Cationic surfactants-modified natural zeolites: improvement of the excipients functionality.

PubMed

Krajisnik, Danina; Milojević, Maja; Malenović, Anđelija; Daković, Aleksandra; Ibrić, Svetlana; Savić, Snezana; Dondur, Vera; Matijasević, Srđan; Radulović, Aleksandra; Daniels, Rolf; Milić, Jela

2010-10-01

In this study an investigation of cationic surfactants-modified natural zeolites as drug formulation excipient was performed. The aim of this work was to carry out a study of the purified natural zeolitic tuff with high amount of clinoptilolite as a potential carrier for molecules of pharmaceutical interest. Two cationic surfactants (benzalkonium chloride and hexadecyltrimethylammonium bromide) were used for modification of the zeolitic surface in two levels (equal to and twice as external cation-exchange capacity of the zeolitic tuff). Prepared samples were characterized by Fourier transform infrared spectroscopy, thermogravimetric, high-performance liquid chromatography analysis, and powder flow determination. Different surfactant/zeolite composites were used for additional investigation of three model drugs: diclofenac diethylamine, diclofenac sodium, and ibuprofen by means of adsorption isotherm measurements in aqueous solutions. The modified zeolites with two levels of surfactant coverage within the short activation time were prepared. Determination of flow properties showed that modification of zeolitic surface reflected on powder flow characteristics. Investigation of the model drugs adsorption on the obtained composites revealed that a variation between adsorption levels was influenced by the surfactant type and the amount present at the surface of the composites. In vitro release profiles of the drugs from the zeolite-surfactant-drug composites revealed that sustained drug release could be attained over a period of 8 hours. The presented results for drug uptake by surfactant-zeolite composites and the afterward drug release demonstrated the potential use of investigated modified natural zeolite as excipients for advanced excipients in drug formulations.

Actinide Sorption in Rainier Mesa Tunnel Waters from the Nevada Test Site

DOE Office of Scientific and Technical Information (OSTI.GOV)

Zhao, P; Zavarin, M; Leif, R

2007-12-17

The sorption behavior of americium (Am), plutonium (Pu), neptunium (Np), and uranium (U) in perched Rainier Mesa tunnel water was investigated. Both volcanic zeolitized tuff samples and groundwater samples were collected from Rainier Mesa, Nevada Test Site, NV for a series of batch sorption experiments. Sorption in groundwater with and without the presence of dissolved organic matter (DOM) was investigated. Am(III) and Pu(IV) are more soluble in groundwater that has high concentrations of DOM. The sorption K{sub d} for Am(III) and Pu(IV) on volcanic zeolitized tuff was up to two orders of magnitude lower in samples with high DOM (15more » to 19 mg C/L) compared to samples with DOM removed (< 0.4 mg C/L) or samples with naturally low DOM (0.2 mg C/L). In contrast, Np(V) and U(VI) sorption to zeolitized tuff was much less affected by the presence of DOM. The Np(V) and U(VI) sorption Kds were low under all conditions. Importantly, the DOM was not found to significantly sorb to the zeolitized tuff during these experiment. The concentration of DOM in groundwater affects the transport behavior of actinides in the subsurface. The mobility of Am(III) and Pu(IV) is significantly higher in groundwater with elevated levels of DOM resulting in potentially enhanced transport. To accurately model the transport behavior of actinides in groundwater at Rainier Mesa, the low actinide Kd values measured in groundwater with high DOM concentrations must be incorporated in predictive transport models.« less

Degraded dryland rehabilitation: boosting seedling survival using zeolitic tuff

NASA Astrophysics Data System (ADS)

Alhamad, Mohammad Noor; Alrbabah, Mohammad; Athamneh, Hana

2016-04-01

More than 90% of Jordan is broadly defined as rangelands. Most rangelands are located within the arid zone of the country. Extensive grazing occurs across much of the natural pastures resulting in serious environmental degradation of natural resources in these rangelands. Several programs were carried out for rangeland conservation and rehabilitation in the country. However, these programs face a major challenge of the low survival rate of transplanted shrub seedlings. Seeking innovative approaches to assure healthy establishment of seedling is a big challenge to achieve successful rehabilitation programs. Drought is considered one of the major problems in rehabilitation. Promoting survival and growth, using zeolitic tuff added to planting holes is suggested to be a possible solution. The experiment was conducted on a factorial arrangement within RCBD design. Two shrub species (Atriplex halimus, Atriplex nummularia) were transplanted into holes prepared with three levels of tuff treatments (mulching, mixing and control) under rainfed condition. The result showed insignificant effect of tuff on seedling survival percentage, when mixing tuff with plantation soil or adding tuff as mulch. Also, the two species showed similar survival percentages over two measured dates. However, mixing tuff with soil during hole preparation significantly enhanced seedling heights. Furthers, The Australian atriplex (Atriplex nummularia) species significantly grow higher than Atriplex halimus. The study results suggested that mixing zeoltic tuff with soil during transplantation of seedling is promising in improving the success of rangeland rehabilitation in dry areas in Jordan.

Geologic evaluation of six nonwelded tuff sites in the vicinity of Yucca Mountain, Nevada for a surface-based test facility for the Yucca Mountain Project

DOE Office of Scientific and Technical Information (OSTI.GOV)

Broxton, D.E.; Chipera, S.J.; Byers, F.M. Jr.

1993-10-01

Outcrops of nonwelded tuff at six locations in the vicinity of Yucca Mountain, Nevada, were examined to determine their suitability for hosting a surface-based test facility for the Yucca Mountain Project. Investigators will use this facility to test equipment and procedures for the Exploratory Studies Facility and to conduct site characterization field experiments. The outcrops investigated contain rocks that include or are similar to the tuffaceous beds of Calico Hills, an important geologic and hydrologic barrier between the potential repository and the water table. The tuffaceous beds of Calico Hills at the site of the potential repository consist of bothmore » vitric and zeolitic tuffs, thus three of the outcrops examined are vitric tuffs and three are zeolitic tuffs. New data were collected to determine the lithology, chemistry, mineralogy, and modal petrography of the outcrops. Some preliminary data on hydrologic properties are also presented. Evaluation of suitability of the six sites is based on a comparison of their geologic characteristics to those found in the tuffaceous beds of Calico Hills within the exploration block.« less

Multiple episodes of zeolite deposition in fractured silicic tuff

DOE Office of Scientific and Technical Information (OSTI.GOV)

Carlos, B.A.; Chipera, S.J.; Snow, M.G.

Fractures in silicic tuffs above the water table at Yucca Mountain, Nevada, USA contain two morphologies of heulandite with different compositions. Tabular heulandite is zoned, with Sr-rich cores and Mg-rich rims. Later prismatic heulandite is nearly the same composition as the more magnesian rims. Heulandite and stellerite may occur between layers of calcite, and calcite occurs locally between generations of heulandite. Thermodynamic modeling, using estimated thermodynamic data and observed chemical compositions for heulandite and stellerite, shows that stellerite is the favored zeolite unless Ca concentrations are reduced or Mg and/or Sr concentrations are significantly elevated above current Yucca Mountain waters.

Oligocene lacustrine tuff facies, Abu Treifeya, Cairo-Suez Road, Egypt

NASA Astrophysics Data System (ADS)

Abdel-Motelib, Ali; Kabesh, Mona; El Manawi, Abdel Hamid; Said, Amir

2015-02-01

Field investigations in the Abu Treifeya area, Cairo-Suez District, revealed the presence of Oligocene lacustrine volcaniclastic deposits of lacustrine sequences associated with an Oligocene rift regime. The present study represents a new record of lacustrine zeolite deposits associated with saponite clay minerals contained within reworked clastic vitric tuffs. The different lithofacies associations of these clastic sequences are identified and described: volcaniclastic sedimentary facies represent episodic volcaniclastic reworking, redistribution and redeposition in a lacustrine environment and these deposits are subdivided into proximal and medial facies. Zeolite and smectite minerals are mainly found as authigenic crystals formed in vugs or crusts due to the reaction of volcanic glasses with saline-alkaline water or as alteration products of feldspars. The presence of abundant smectite (saponite) may be attributed to a warm climate, with alternating humid and dry conditions characterised by the existence of kaolinite. Reddish iron-rich paleosols record periods of non-deposition intercalated with the volcaniclastic tuff sequence.

Radionuclide sorption in Yucca Mountain tuffs with J-13 well water: Neptunium, uranium, and plutonium. Yucca Mountain site characterization program milestone 3338

DOE Office of Scientific and Technical Information (OSTI.GOV)

Triay, I.R.; Cotter, C.R.; Kraus, S.M.

1996-08-01

We studied the retardation of actinides (neptunium, uranium, and plutonium) by sorption as a function of radionuclide concentration in water from Well J-13 and of tuffs from Yucca Mountain. Three major tuff types were examined: devitrified, vitric, and zeolitic. To identify the sorbing minerals in the tuffs, we conducted batch sorption experiments with pure mineral separates. These experiments were performed with water from Well J-13 (a sodium bicarbonate groundwater) under oxidizing conditions in the pH range from 7 to 8.5. The results indicate that all actinides studied sorb strongly to synthetic hematite and also that Np(V) and U(VI) do notmore » sorb appreciably to devitrified or vitric tuffs, albite, or quartz. The sorption of neptunium onto clinoptilolite-rich tuffs and pure clinoptilolite can be fitted with a sorption distribution coefficient in the concentration range from 1 X 10{sup -7} to 3 X 10{sup -5} M. The sorption of uranium onto clinoptilolite-rich tuffs and pure clinoptilolite is not linear in the concentration range from 8 X 10{sup -8} to 1 X 10{sup -4} M, and it can be fitted with nonlinear isotherm models (such as the Langmuir or the Freundlich Isotherms). The sorption of neptunium and uranium onto clinoptilolite in J-13 well water increases with decreasing pH in the range from 7 to 8.5. The sorption of plutonium (initially in the Pu(V) oxidation state) onto tuffs and pure mineral separates in J-13 well water at pH 7 is significant. Plutonium sorption decreases as a function of tuff type in the order: zeolitic > vitric > devitrified; and as a function of mineralogy in the order: hematite > clinoptilolite > albite > quartz.« less

Comparison of neptunium sorption results using batch and column techniques

DOE Office of Scientific and Technical Information (OSTI.GOV)

Triay, I.R.; Furlano, A.C.; Weaver, S.C.

1996-08-01

We used crushed-rock columns to study the sorption retardation of neptunium by zeolitic, devitrified, and vitric tuffs typical of those at the site of the potential high-level nuclear waste repository at Yucca Mountain, Nevada. We used two sodium bicarbonate waters (groundwater from Well J-13 at the site and water prepared to simulate groundwater from Well UE-25p No. 1) under oxidizing conditions. It was found that values of the sorption distribution coefficient, Kd, obtained from these column experiments under flowing conditions, regardless of the water or the water velocity used, agreed well with those obtained earlier from batch sorption experiments undermore » static conditions. The batch sorption distribution coefficient can be used to predict the arrival time for neptunium eluted through the columns. On the other hand, the elution curves showed dispersivity, which implies that neptunium sorption in these tuffs may be nonlinear, irreversible, or noninstantaneous. As a result, use of a batch sorption distribution coefficient to calculate neptunium transport through Yucca Mountain tuffs would yield conservative values for neptunium release from the site. We also noted that neptunium (present as the anionic neptunyl carbonate complex) never eluted prior to tritiated water, which implies that charge exclusion does not appear to exclude neptunium from the tuff pores. The column experiments corroborated the trends observed in batch sorption experiments: neptunium sorption onto devitrified and vitric tuffs is minimal and sorption onto zeolitic tuffs decreases as the amount of sodium and bicarbonate/carbonate in the water increases.« less

DOE Office of Scientific and Technical Information (OSTI.GOV)

Connolly, J.R.

Petrologic, bulk chemical, and mineralogic data are presented for 49 samples of tuffaceous rocks from core holes USW G-1 and UE-25a{number_sign}1 at Yucca Mountain, Nevada. Included, in descending stratigraphic order, are 11 samples from the Topopah Spring Member of the Paintbrush Tuff, 12 samples from the Tuffaceous Beds of Calico Hills, 3 samples from the Prow Pass Member of the Crater Flat Tuff, 20 samples from the Bullfrog Member of the Crater Flat Tuff and 3 samples from the Tram Member of the Crater Flat Tuff. The suite of samples contains a wide variety of petrologic types, including zeolitized, glassy,more » and devitrified tuffs. Data vary considerably between groups of samples, and include thin section descriptions (some with modal analyses for which uncertainties are estimated), electron microprobe analyses of mineral phases and matrix, mineral identifications by X-ray diffraction, and major element analyses with uncertainty estimates.« less

Preliminary hydrogeologic assessment of boreholes UE-25c #1, UE-25c #2, and UE-25c #3, Yucca Mountain, Nye County, Nevada

USGS Publications Warehouse

Geldon, A.L.

1993-01-01

Boreholes UE-25c #1, UE-25c #2, and UE-25c #3 (collectively called the C-holes) each were drilled to a depth of 914.4 meters at Yucca Mountain, on the Nevada Test Site, in 1983 and 1984 for the purpose of conducting aquifer and tracer tests. Each of the boreholes penetrated the Paintbrush Tuff and the tuffs and lavas of Calico Hills and bottomed in the Crater Flat Tuff. The geologic units penetrated consist of devitrified to vitrophyric, nonwelded to densely welded, ash-flow tuff, tuff breccia, ash-fall tuff, and bedded tuff. Below the water table, which is at an average depth of 401.6 meters below land surface, the rocks are argillic and zeolitic. The geologic units at the C-hole complex strike N. 2p W. and dip 15p to 21p NE. They are cut by several faults, including the Paintbrush Canyon Fault, a prominent normal fault oriented S. 9p W., 52.2p NW. The rocks at the C-hole complex are fractured extensively, with most fractures oriented approximately perpendicular to the direction of regional least horizontal principal stress. In the Crater Flat Tuff and the tuffs and lavas of Calico Hills, fractures strike predominantly between S. 20p E. and S. 20p W. and secondarily between S. 20p E. and S. 60p E. In the Topopah Spring Member of the Paintbrush Tuff, however, southeasterly striking fractures predominate. Most fractures are steeply dipping, although shallowly dipping fractures occur in nonwelded and reworked tuff intervals of the Crater Flat Tuff. Mineral-filled fractures are common in the tuff breccia zone of the Tram Member of the Crater Flat Tuff, and, also, in the welded tuff zone of the Bullfrog Member of the Crater Flat Tuff. The fracture density of geologic units in the C-holes was estimated to range from 1.3 to 7.6 fractures per cubic meter. Most of these estimates appear to be the correct order of magnitude when compared to transect measurements and core data from other boreholes 1.3 orders of magnitude too low. Geophysical data and laboratory analyses were used to determine matrix hydrologic properties of the tuffs and lavas of Calico Hills and the Crater Flat Tuff in the C-holes. The porosity ranged from 12 to 43 percent and, on the average, was larger in nonwelded to partially welded, ash-flow tuff, ashfall tuff, and reworked tuff than in moderately to densely welded ash-flow tuff. The pore-scale horizontal permeability of nine samples ranged from 5.7x10'3 to 2.9 millidarcies, and the pore-scale vertical permeability of these samples ranged from 3.7x10'* to 1.5 millidarcies. Ratios of pore-scale horizontal to vertical permeability generally ranged from 0.7 to 2. Although the number of samples was small, values of pore-scale permeability determined were consistent with samples from other boreholes at Yucca Mountain. The specific storage of nonwelded to partially welded ash-flow tuff, ash-fall tuff, and reworked tuff was estimated from porosity and elasticity to' be 2xlO'6 per meter, twice the specific storage of moderately to densely welded ash-flow tuff and tuff breccia. The storativity of geologic units, based on their average thickness (corrected for bedding dip) and specific storage, was estimated to range from 1xlO's to 2xlO'4. Ground-water flow in the Tertiary rocks of the Yucca Mountain area is not confined by strata but appears to result from the random intersection of water-bearing fractures and faults. Even at the C-hole complex, an area of only 1,027 square meters, water-producing zones during pumping tests vary from borehole to borehole. In borehole UE-25c #1, water is produced mainly from the lower, nonwelded to welded zone of the Bullfrog Member of the Crater Flat Tuff and secondarily from the tuff-breccia zone of the Tram Member of the Crater Flat Tuff. In borehole UE-25c #3, water is produced in nearly equal proportions from these two intervals and the central, moderately to densely welded zone of the Bullfrog Member. In borehole UE-25c #2, almost all production comes from the moderately to dense

Methods for pore water extraction from unsaturated zone tuff, Yucca Mountain, Nevada

USGS Publications Warehouse

Scofield, K.M.

2006-01-01

Assessing the performance of the proposed high-level radioactive waste repository at Yucca Mountain, Nevada, requires an understanding of the chemistry of the water that moves through the host rock. The uniaxial compression method used to extract pore water from samples of tuffaceous borehole core was successful only for nonwelded tuff. An ultracentrifugation method was adopted to extract pore water from samples of the densely welded tuff of the proposed repository horizon. Tests were performed using both methods to determine the efficiency of pore water extraction and the potential effects on pore water chemistry. Test results indicate that uniaxial compression is most efficient for extracting pore water from nonwelded tuff, while ultracentrifugation is more successful in extracting pore water from densely welded tuff. Pore water splits collected from a single nonwelded tuff core during uniaxial compression tests have shown changes in pore water chemistry with increasing pressure for calcium, chloride, sulfate, and nitrate. Pore water samples collected from the intermediate pressure ranges should prevent the influence of re-dissolved, evaporative salts and the addition of ion-deficient water from clays and zeolites. Chemistry of pore water splits from welded and nonwelded tuffs using ultracentrifugation indicates that there is no substantial fractionation of solutes.

Zeolite-clay mineral zonation of volcaniclastic sediments within the McDermitt caldera complex of Nevada and Oregon

USGS Publications Warehouse

Glanzman, Richard K.; Rytuba, James J.

1979-01-01

Volcaniclastic sediments deposited in the moat of the collapsed McDermitt caldera complex have been altered chiefly to zeolites and potassium feldspar. The original rhyolitic and peralkaline ash-flow tuffs are included in conglomerates at the caldera rims and grade into a lacustrine series near the center of the collapse. The tuffs show a lateral zeolitic alteration from almost fresh glass to clinoptilolite, clinoptilolite-mordenite, and erionite; to analcime-potassium feldspar; and finally to potassium feldspar. Vertical zonation is in approximately the same order. Clay minerals in associated mudstones, on the other hand, show little lateral variation but a distinct vertical zonation, having a basal dioctahedral smectite, a medial trioctahedral smectite, and an upper dioctahedral smectite. The medial trioctahedral smectite is enriched in lithium (as much as 6,800 ppm Li). Hydrothermal alteration of the volcaniclastic sediments, forming both mercury and uranium deposits, caused a distinct zeolite and clay-mineral zonation within the general lateral zonation. The center of alteration is generally potassium feldspar, commonly associated with alunite. Potassium feldspar grades laterally and vertically to either clinoptilolite or clinoptilolite-mordenite, generally associated with gypsum. This zone then grades vertically and laterally into fresh glass. The clay minerals are a dioctahedral smectite, a mixed-layer clay mineral, and a 7-A clay mineral. The mixed-layer and 7-A clay minerals are associated with the potassium feldspar-alunite zone of alteration, and the dioctahedral smectite is associated with clinoptilolite. This mineralogical zonation may be an exploration guide for mercury and uranium mineralization in the caldera complex environment.

Effect of reducing groundwater on the retardation of redox-sensitive radionuclides

PubMed Central

Hu, QH; Zavarin, M; Rose, TP

2008-01-01

Laboratory batch sorption experiments were used to investigate variations in the retardation behavior of redox-sensitive radionuclides. Water-rock compositions were designed to simulate subsurface conditions at the Nevada Test Site (NTS), where a suite of radionuclides were deposited as a result of underground nuclear testing. Experimental redox conditions were controlled by varying the oxygen content inside an enclosed glove box and by adding reductants into the testing solutions. Under atmospheric (oxidizing) conditions, radionuclide distribution coefficients varied with the mineralogic composition of the sorbent and the water chemistry. Under reducing conditions, distribution coefficients showed marked increases for 99Tc (from 1.22 at oxidizing to 378 mL/g at mildly reducing conditions) and 237Np (an increase from 4.6 to 930 mL/g) in devitrified tuff, but much smaller variations in alluvium, carbonate rock, and zeolitic tuff. This effect was particularly important for 99Tc, which tends to be mobile under oxidizing conditions. A review of the literature suggests that iodine sorption should decrease under reducing conditions when I- is the predominant species; this was not consistently observed in batch tests. Overall, sorption of U to alluvium, devitrified tuff, and zeolitic tuff under atmospheric conditions was less than in the glove-box tests. However, the mildly reducing conditions achieved here were not likely to result in substantial U(VI) reduction to U(IV). Sorption of Pu was not affected by the decreasing Eh conditions achieved in this study, as the predominant sorbed Pu species in all conditions was expected to be the low-solubility and strongly sorbing Pu(OH)4. Depending on the aquifer lithology, the occurrence of reducing conditions along a groundwater flowpath could potentially contribute to the retardation of redox-sensitive radionuclides 99Tc and 237Np, which are commonly identified as long-term dose contributors in the risk assessment in various radionuclide environmental contamination scenarios. The implications for increased sorption of 99Tc and 237Np to devitrified tuff under reducing conditions are significant as the fractured devitrified tuff serves as important water flow path at the NTS and the horizon for a proposed repository to store high-level nuclear waste at Yucca Mountain. PMID:19077277

DOE Office of Scientific and Technical Information (OSTI.GOV)

Hu, Q; Zavarin, M; Rose, T P

Laboratory batch sorption experiments were used to investigate variations in the retardation behavior of redox-sensitive radionuclides. Water-rock compositions used during these experiments were designed to simulate subsurface conditions at the Nevada Test Site (NTS), where a suite of radionuclides were deposited as a result of underground nuclear testing. Experimental redox conditions were controlled by varying the oxygen content inside an enclosed glove box and by adding reductants into the testing solutions. Under atmospheric (oxidizing) conditions, the radionuclide distribution coefficients varied with the mineralogical composition of the sorbent and the water chemistry. Under reducing conditions, distribution coefficients showed marked increases formore » {sup 99}Tc and {sup 237}Np in devitrified tuff, but much smaller variations in alluvium, carbonate rock, and zeolitic tuff. This effect was particularly important for {sup 99}Tc, which tends to be mobile under oxidizing conditions. Unlike other redox-sensitive radionuclides, iodine sorption may decrease under reducing conditions when I{sup -} is the predominant species. Overall, sorption of U to alluvium, devitrified tuff, and zeolitic tuff under atmospheric conditions was less than in the glove-box tests. However, the mildly reducing conditions achieved here were not likely to result in substantial U(VI) reduction to U(IV). Sorption of Pu was not affected by the decreasing redox conditions achieved in this study, as the predominant sorbed Pu species in all conditions was expected to be the low-solubility and strongly sorbing Pu(OH){sub 4}. Depending on the aquifer lithology, the occurrence of reducing conditions along a groundwater flowpath could potentially contribute to the retardation of redox-sensitive radionuclides {sup 99}Tc and {sup 237}Np, which are commonly identified as long-term dose contributors in the risk assessment in various nuclear facilities.« less

Slanic Tuff and associated Miocene evaporite deposits, Eastern Carpathians, Romania

NASA Astrophysics Data System (ADS)

Bojar, Ana-Voica; Halas, Stanislaw; Barbu, Victor; Bojar, Hans-Peter; Wojtowicz, Artur; Duliu, Octavian

2017-04-01

Miocene tuffs of calcalkaline composition are widespread in the Carpathians, Pannonian and Eastern Alpine realm. Their occurrences are described in outcrops as well as in the subsurface. The presence of such tuffs may offer important criteria for stratigraphic correlations and help to establish the absolute age of deposits and associated climatic and environmental changes. The Green Stone Hill (Muntele Piatra Verde) is situated to the north of Slanic-Prahova salt mine, in the bend region of the Eastern Carpathians, Romania. From bottom to top the section is composed of: marls with Globigerina followed by the so called Slanic tuff, gypsum and salt breccia and, on the top, radiolarian bearing shales. The stratigraphic age of the section is Middle to Upper Badenian (nannoplankton zones NN5 to NN6). XRD investigations of the green Slanic tuff show that the main mineralogical component is clinoptilolite (zeolite) followed by quartz and plagioclase. For this type of tuff there is no crystalline phase, which may be used for radiometric dating. In the middle part of the green tuff interval, we found discrete layers of a much coarser white tuff, with mineralogy consisting of quartz, plagioclase, biotite and clinoptilolite. The white tuff forming distinct layers within the green tuff, has an andesitic composition. 40Ar/39Ar dating of biotite concentrates from the white tuff gives an age of 13.6±0.2Ma, the dated layer being situated below the gypsum and salt breccia. We consider that the age is well constraining the time when the green tuffs were formed at the border of the basin. From this level upwards discrete gypsum layers occurs within the green tuffs, the age may be considered as indicating the base of the evaporitic sequence. To the south-east, from this level upwards evaporites, mainly salt formed. The age suggests that evaporitic deposits formed after the Mid Badenian climatic optimum, evaporitic formation being related to restricted circulation due the drop of sea-level and tectonism.

Rare earth elements upon assessment of reasons of the geophagy in Sikhote-Alin region (Russian Federation), Africa and other world regions.

PubMed

Panichev, Alexander M; Popov, Vladimir K; Chekryzhov, Igor Yu; Seryodkin, Ivan V; Stolyarova, Tatiana A; Zakusin, Sergey V; Sergievich, Alexandr A; Khoroshikh, Pavel P

2016-12-01

Rocks eaten by wild animals on the Bolshoy Shanduyskiy kudur in the Sikhote-Alin region (Russian Federation) are zeolite-clay mineral complexes-products of weathering of zeolitized vitric tuffs of rhyolite composition, deposited in aqueous medium within the volcanic caldera of about 55 million years ago. By composition of rock-forming oxides, the tuffs refer to high-potassium calc-alkaline series. In trace elements of most favorite kudurites of the Bolshoy Shanduyskiy kudur, there are significantly increased contents of most of rare earth elements (2-5 times in comparison with surrounding rocks). The results of our analysis of geological and geochemical data on kudurs and kudurites in another part of the Sikhote-Alin, as well as on other regions of the world (particularly, in Africa and Indonesia), taking into account new data on the prevalence of rare earth elements in living matter and their medical and biological properties, enable us to consider the version of causal connection of the geophagy with rare earth elements.

Reducing Uncertainty in the Distribution of Hydrogeologic Units within Volcanic Composite Units of Pahute Mesa Using High-Resolution 3-D Resistivity Methods, Nevada Test Site, Nevada

USGS Publications Warehouse

Rodriguez, Brian D.; Sweetkind, Don; Burton, Bethany L.

2010-01-01

The U.S. Department of Energy (DOE) and the National Nuclear Security Administration (NNSA) at their Nevada Site Office (NSO) are addressing groundwater contamination resulting from historical underground nuclear testing through the Environmental Management program and, in particular, the Underground Test Area (UGTA) project. From 1951 to 1992, 828 underground nuclear tests were conducted at the Nevada Test Site (NTS) northwest of Las Vegas (DOE UGTA, 2003). Most of these tests were conducted hundreds of feet above the groundwater table; however, more than 200 of the tests were near, or within, the water table. This underground testing was limited to specific areas of the NTS including Pahute Mesa, Rainier Mesa/Shoshone Mountain, Frenchman Flat, and Yucca Flat. Volcanic composite units make up much of the area within the Pahute Mesa Corrective Action Unit (CAU) at the NTS, Nevada. The extent of many of these volcanic composite units extends throughout and south of the primary areas of past underground testing at Pahute and Rainier Mesas. As situated, these units likely influence the rate and direction of groundwater flow and radionuclide transport. Currently, these units are poorly resolved in terms of their hydrologic properties introducing large uncertainties into current CAU-scale flow and transport models. In 2007, the U.S. Geological Survey (USGS), in cooperation with DOE and NNSA-NSO acquired three-dimensional (3-D) tensor magnetotelluric data at the NTS in Area 20 of Pahute Mesa CAU. A total of 20 magnetotelluric recording stations were established at about 600-m spacing on a 3-D array and were tied to ER20-6 well and other nearby well control (fig. 1). The purpose of this survey was to determine if closely spaced 3-D resistivity measurements can be used to characterize the distribution of shallow (600- to 1,500-m-depth range) devitrified rhyolite lava-flow aquifers (LFA) and zeolitic tuff confining units (TCU) in areas of limited drill hole control on Pahute Mesa within the Calico Hills zeolitic volcanic composite unit (VCU), an important hydrostratigraphic unit in Area 20. The resistivity response was evaluated and compared with existing well data and hydrogeologic unit tops from the current Pahute Mesa framework model. In 2008, the USGS processed and inverted the magnetotelluric data into a 3-D resistivity model. We interpreted nine depth slices and four west-east profile cross sections of the 3-D resistivity inversion model. This report documents the geologic interpretation of the 3-D resistivity model. Expectations are that spatial variations in the electrical properties of the Calico Hills zeolitic VCU can be detected and mapped with 3-D resistivity, and that these changes correlate to differences in rock permeability. With regard to LFA and TCU, electrical resistivity and permeability are typically related. Tuff confining units will typically have low electrical resistivity and low permeability, whereas LFA will have higher electrical resistivity and zones of higher fracture-related permeability. If expectations are shown to be correct, the method can be utilized by the UGTA scientists to refine the hydrostratigraphic unit (HSU) framework in an effort to more accurately predict radionuclide transport away from test areas on Pahute and Rainier Mesas.

Zeolitization of intracaldera sediments and rhyolitic rocks in the 1.25 Ma lake of Valles caldera, New Mexico, USA

NASA Astrophysics Data System (ADS)

Chipera, Steve J.; Goff, Fraser; Goff, Cathy J.; Fittipaldo, Melissa

2008-12-01

Quantitative X-ray diffraction analysis of about 80 rhyolite and associated lacustrine rocks has characterized previously unrecognized zeolitic alteration throughout the Valles caldera resurgent dome. The alteration assemblage consists primarily of smectite-clinoptilolite-mordenite-silica, which replaces groundmass and fills voids, especially in the tuffs and lacustrine rocks. Original rock textures are routinely preserved. Mineralization typically extends to depths of only a few tens of meters and resembles shallow "caldera-type zeolitization" as defined by Utada et al. [Utada, M., Shimizu, M., Ito, T., Inoue, A., 1999. Alteration of caldera-forming rocks related to the Sanzugawa volcanotectonic depression, northeast Honshu, Japan — with special reference to "caldera-type zeolitization." Resource Geol. Spec. Issue No. 20, 129-140]. Geology and 40Ar/ 39Ar dates limit the period of extensive zeolite growth to roughly the first 30 kyr after the current caldera formed (ca. 1.25 to 1.22 Ma). Zeolitic alteration was promoted by saturation of shallow rocks with alkaline lake water (a mixture of meteoric waters and degassed hydrothermal fluids) and by high thermal gradients caused by cooling of the underlying magma body and earliest post-caldera rhyolite eruptions. Zeolitic alteration of this type is not found in the later volcanic and lacustrine rocks of the caldera moat (≤ 0.8 Ma) suggesting that later lake waters were cooler and less alkaline. The shallow zeolitic alteration does not have characteristics resembling classic, alkaline lake zeolite deposits (no analcime, erionite, or chabazite) nor does it contain zeolites common in high-temperature hydrothermal systems (laumontite or wairakite). Although aerially extensive, the early zeolitic alteration does not form laterally continuous beds and are consequently, not of economic significance.

Stratigraphic and volcano-tectonic relations of Crater Flat Tuff and some older volcanic units, Nye County, Nevada

USGS Publications Warehouse

Carr, W.J.; Byers, F.M.; Orkild, Paul P.

1984-01-01

The Crater Flat Tuff is herein revised to include a newly recognized lowest unit, the Tram Member, exposed at scattered localities in the southwest Nevada Test Site region, and in several drill holes in the Yucca Mountain area. The overlying Bullfrog and Prow Pass Members are well exposed at the type locality of the formation near the southeast edge of Crater Flat, just north of U.S. Highway 95. In previous work, the Tram Member was thought to be the Bullfrog Member, and therefore was shown as Bullfrog or as undifferentiated Crater Flat Tuff on published maps. The revised Crater Flat Tuff is stratigraphically below the Topopah Spring Member of the Paintbrush Tuff and above the Grouse Canyon Member of the Belted Range Tuff, and is approximately 13.6 m.y. old. Drill holes on Yucca Mountain and near Fortymile Wash penetrate all three members of the Crater Flat as well as an underlying quartz-poor unit, which is herein defined as the Lithic Ridge Tuff from exposures on Lithic Ridge near the head of Topopah Wash. In outcrops between Calico Hills and Yucca Flat, the Lithic Ridge Tuff overlies a Bullfrog-like unit of reverse magnetic polarity that probably correlates with a widespread unit around and under Yucca Flat, referred to previously as Crater Flat Tuff. This unit is here informally designated as the tuff of Yucca Flat. Although older, it may be genetically related to the Crater Flat Tuff. Although the rocks are poorly exposed, geophysical and geologic evidence to date suggests that (1) the source of the Crater Flat Tuff is a caldera complex in the Crater Flat area between Yucca Mountain and Bare Mountain, and (2) there are at least two cauldrons within this complex--one probably associated with eruption of the Tram, the other with the Bullfrog and Prow Pass Members. The complex is named the Crater Flat-Prospector Pass caldera complex. The northern part of the Yucca Mountain area is suggested as the general location of the source of pre-Crater Flat tuffs, but a caldera related to the Lithic Ridge Tuff has not been specifically identified.

Two examples of subaqueously welded ash-flow tuffs: the Visean of southern Vosges (France) and the Upper Cretaceous of northern Anatolia (Turkey)

NASA Astrophysics Data System (ADS)

Schneider, Jean-Luc; Fourquin, Claude; Paicheler, Jean-Claude

1992-02-01

Pyroclastic deposits interpreted as subaqueous ash-flow tuff have been recognized within Archean to Recent marine and lacustrine sequences. Several authors proposed a high-temperature emplacement for some of these tuffs. However, the subaqueous welding of pyroclastic deposits remains controversial. The Visean marine volcaniclastic formations of southern Vosges (France) contain several layers of rhyolitic and rhyodacitic ash-flow tuff. These deposits include, from proximal to distal settings, breccia, lapilli and fine-ash tuff. The breccia and lapilli tuff are partly welded, as indicated by the presence of fiamme, fluidal and axiolitic structures. The lapilli tuff form idealized sections with a lower, coarse and welded unit and an upper, bedded and unwelded fine-ash tuff. Sedimentary structures suggest that the fine-ash tuff units were deposited by turbidity currents. Welded breccias, interbedded in a thick submarine volcanic complex, indicate the close proximity of the volcanic source. The lapilli and fine-ash tuff are interbedded in a thick marine sequence composed of alternating sandstones and shales. Presence of a marine stenohaline fauna and sedimentary structures attest to a marine depositional environment below storm-wave base. In northern Anatolia, thick massive sequences of rhyodacitic crystal tuff are interbedded with the Upper Cretaceous marine turbidites of the Mudurnu basin. Some of these tuffs are welded. As in southern Vosges, partial welding is attested by the presence of fiamme and fluidal structures. The latter are frequent in the fresh vitric matrix. These tuff units contain a high proportion of vitroclasis, and were emplaced by ash flows. Welded tuff units are associated with non-welded crystal tuff, and contain abundant bioclasts which indicate mixing with water during flowage. At the base, basaltic breccia beds are associated with micritic beds containing a marine fauna. The welded and non-welded tuff sequences are interbedded in an alternation of limestones and marls. These limestones are rich in pelagic microfossils. The evidence above strongly suggest that in both examples, tuff beds are partly welded and were emplaced at high temperature by subaqueous ash flows in a permanent marine environment. The sources of the pyroclastic material are unknown in both cases. We propose that the ash flows were produced during submarine fissure eruptions. Such eruptions could produce non-turbulent flows which were insulated by a steam carapace before deposition and welding. The welded ash-flow tuff deposits of southern Vosges and northern Anatolia give strong evidence for existence of subaqueous welding.

Hydrology of Yucca Mountain, Nevada

USGS Publications Warehouse

Flint, A.L.; Flint, L.E.; Kwicklis, E.M.; Bodvarsson, G.S.; Fabryka-Martin, J. M.

2001-01-01

Yucca Mountain, located in southern Nevada in the Mojave Desert, is being considered as a geologic repository for high-level radioactive waste. Although the site is arid, previous studies indicate net infiltration rates of 5-10 mm yr-1 under current climate conditions. Unsaturated flow of water through the mountain generally is vertical and rapid through the fractures of the welded tuffs and slow through the matrix of the nonwelded tuffs. The vitric-zeolitic boundary of the nonwelded tuffs below the potential repository, where it exists, causes perching and substantial lateral flow that eventually flows through faults near the eastern edge of the potential repository and recharges the underlying groundwater system. Fast pathways are located where water flows relatively quickly through the unsaturated zone to the water table. For the bulk of the water a large part of the travel time from land surface to the potential repository horizon (~300 m below land surface) is through the interlayered, low fracture density, nonwelded tuff where flow is predominately through the matrix. The unsaturated zone at Yucca Mountain is being modeled using a three-dimensional, dual-continuum numerical model to predict the results of measurements and observations in new boreholes and excavations. The interaction between experimentalists and modelers is providing confidence in the conceptual model and the numerical model and is providing researchers with the ability to plan further testing and to evaluate the usefulness or necessity of further data collection.

Novel kinetic model of the removal of divalent heavy metal ions from aqueous solutions by natural clinoptilolite.

PubMed

Jovanovic, Mina; Rajic, Nevenka; Obradovic, Bojana

2012-09-30

Removal of heavy metal ions from aqueous solutions using zeolites is widely described by pseudo-second order kinetics although this model may not be valid under all conditions. In this work, we have extended approaches used for derivation of this model in order to develop a novel kinetic model that is related to the ion exchange mechanism underlying sorption of metal ions in zeolites. The novel model assumed two reversible steps, i.e. release of sodium ions from the zeolite lattice followed by bonding of the metal ion. The model was applied to experimental results of Cu(II) sorption by natural clinoptilolite-rich zeolitic tuff at different initial concentrations and temperatures and then validated by predictions of ion exchange kinetics of other divalent heavy metal ions (i.e. Mn(II), Zn(II) and Pb(II)). Model predictions were in excellent agreements with experimental data for all investigated systems. In regard to the proposed mechanism, modeling results implied that the sodium ion release rate was constant for all investigated metals while the overall rate was mainly determined by the rate of heavy metal ion bonding to the lattice. In addition, prediction capabilities of the novel model were demonstrated requiring one experimentally determined parameter, only. Copyright © 2012 Elsevier B.V. All rights reserved.

Stochastic modeling of a lava-flow aquifer system

USGS Publications Warehouse

Cronkite-Ratcliff, Collin; Phelps, Geoffrey A.

2014-01-01

This report describes preliminary three-dimensional geostatistical modeling of a lava-flow aquifer system using a multiple-point geostatistical model. The purpose of this study is to provide a proof-of-concept for this modeling approach. An example of the method is demonstrated using a subset of borehole geologic data and aquifer test data from a portion of the Calico Hills Formation, a lava-flow aquifer system that partially underlies Pahute Mesa, Nevada. Groundwater movement in this aquifer system is assumed to be controlled by the spatial distribution of two geologic units—rhyolite lava flows and zeolitized tuffs. The configuration of subsurface lava flows and tuffs is largely unknown because of limited data. The spatial configuration of the lava flows and tuffs is modeled by using a multiple-point geostatistical simulation algorithm that generates a large number of alternative realizations, each honoring the available geologic data and drawn from a geologic conceptual model of the lava-flow aquifer system as represented by a training image. In order to demonstrate how results from the geostatistical model could be analyzed in terms of available hydrologic data, a numerical simulation of part of an aquifer test was applied to the realizations of the geostatistical model.

Hydrothermal convection and mordenite precipitation in the cooling Bishop Tuff, California, USA

NASA Astrophysics Data System (ADS)

Randolph-Flagg, N. G.; Breen, S. J.; Hernandez, A.; Self, S.; Manga, M.

2014-12-01

We present field observations of erosional columns in the Bishop Tuff and then use laboratory results and numerical models to argue that these columns are evidence of relict convection in a cooling ignimbrite. Many square kilometers of the Bishop Tuff have evenly-spaced, vertical to semi-vertical erosional columns, a result of hydrothermal alteration. These altered regions are more competent than the surrounding tuff, are 0.1-0.7 m in diameter, are separated by ~ 1 m, and in some cases are more than 8 m in height. JE Bailey (U. of Hawaii, dissertation, 2005) suggested that similar columns in the Bandelier Tuff were formed when slumping allowed water to pool at the surface of the still-cooling ignimbrite. As water percolated downward it boiled generating evenly spaced convection cells similar to heat pipes. We quantify this conceptual model and apply it the Bishop Tuff to understand the physics within ignimbrite-borne hydrothermal systems. We use thin sections to measure changing porosity and use scanning electron microscope (SEM) and x-ray diffraction (XRD) analyses to show that pore spaces in the columns are cemented by the mineral mordenite, a low temperature zeolite that precipitates between 120-200 oC (Bish et al., 1982), also found in the Bandelier Tuff example. We then use scaling to show 1) that water percolating into the cooling Bishop Tuff would convect and 2) that the geometry and spacing of the columns is predicted by the ignimbrite temperature and permeability. We use the computer program HYDROTHERM (Hayba and Ingebritsen, 1994; Kipp et al., 2008) to model 2-phase convection in the Bishop Tuff. By systematically changing permeability, initial temperature, and topography we can identify the pattern of flows that develop when the ignimbrite is cooled by water from above. Hydrothermally altered columns in ignimbrite are the natural product of coupled heat, mass, and chemical transport and have similarities to other geothermal systems, economic ore deposits, and mid-ocean ridge hydrothermal systems. The columns allow direct observation to constrain complex models of multiphase convection, reactive transport, and permeability. Our results also have paleoclimate implications, implying a large and stable source of water in the SE/SSE Long Valley area immediately after the ~760,000 ka caldera-forming eruption.

Eruptive history, petrology, and petrogenesis of the Joe Lott Tuff Member of the Mount Belknap Volcanics, Marysvale volcanic field, west-central Utah

USGS Publications Warehouse

Budding, Karin E.

1982-01-01

The Joe Lott Tuff Member of the Mount Belknap Volcanics is the largest rhyolitic ash-flow tuff sheet in the Marysvale volcanic field. It was erupted 19 m.y. ago, shortly after the changeover from intermediate-composition calc-alkalic volcanism to bimodal basalt-rhyolite volcanism. Eruption of the tuff resulted in the formation of the Mount Belknap Caldera whose pyroclastic intracaldera stratigraphy parallels that in the outflow facies. The Joe Loft Tuff Member is a composite ash-flow sheet that changes laterally from a simple cooling unit near the source to four distinct cooling units toward the distal end. The lowest of these units is the largest and most widespread; it is 64 m thick and contains a basal vitrophyre. Eruption of the lower unit led to the initial collapse of the caldera. The lower unit is followed upward by a 43 m middle unit, a 26 m pink-colored unit which is separated by a prominent air- fall layer, and a 31 m upper unit. The Joe Loft Tuff Member is an alkali rhyolite with 75.85-77.31 wt. % silica and 8.06-9.32 wt. % K2O+Na2O; the agpaitic index (Na2O+ K2O/Al2O3) is .77-.98. The tuff contains about I% phenocrysts of quartz, sanidine, oligoclase, augite, apatite, zircon, sphene, biotite, and oxidized Fe-Ti oxides. The basal vitrophyre contains accessory allanite, chevkinite, and magnesiohastingsite. The main cooling units are chemically and mineralogically zoned indicating that the magma chamber restratified prior to each major eruption. Within each of the two thickest cooling units, the mineralogy changes systematically upwards; the Or content and relative volume of sanidine decreases and An content of plagioclase increases. The basal vitrophyre of the lower unit has a bulk composition that lies in the thermal trough near the minima of Or-Ab-Q at 1 kb PH2O. Microprobe analyses of feldspar and chemical modeling on experimental systems indicate that pre-eruption temperatures were near 750?C and that the temperature increased during the eruption of the cooling units. The chemical gradients in the apatite and whole-rock data in the Joe Loft Tuff Member and the consistent mineral assemblages throughout the ash-flow cannot be explained by crystal settling. The fractionation of the Joe Lott Tuff Member appears to closer fit the model of convection-driven thermogravitational diffusion.

Evaluation of Pleistocene groundwater flow through fractured tuffs using a U-series disequilibrium approach, Pahute Mesa, Nevada, USA

USGS Publications Warehouse

Paces, James B.; Nichols, Paul J.; Neymark, Leonid A.; Rajaram, Harihar

2013-01-01

Groundwater flow through fractured felsic tuffs and lavas at the Nevada National Security Site represents the most likely mechanism for transport of radionuclides away from underground nuclear tests at Pahute Mesa. To help evaluate fracture flow and matrix–water exchange, we have determined U-series isotopic compositions on more than 40 drill core samples from 5 boreholes that represent discrete fracture surfaces, breccia zones, and interiors of unfractured core. The U-series approach relies on the disruption of radioactive secular equilibrium between isotopes in the uranium-series decay chain due to preferential mobilization of 234U relative to 238U, and U relative to Th. Samples from discrete fractures were obtained by milling fracture surfaces containing thin secondary mineral coatings of clays, silica, Fe–Mn oxyhydroxides, and zeolite. Intact core interiors and breccia fragments were sampled in bulk. In addition, profiles of rock matrix extending 15 to 44 mm away from several fractures that show evidence of recent flow were analyzed to investigate the extent of fracture/matrix water exchange. Samples of rock matrix have 234U/238U and 230Th/238U activity ratios (AR) closest to radioactive secular equilibrium indicating only small amounts of groundwater penetrated unfractured matrix. Greater U mobility was observed in welded-tuff matrix with elevated porosity and in zeolitized bedded tuff. Samples of brecciated core were also in secular equilibrium implying a lack of long-range hydraulic connectivity in these cases. Samples of discrete fracture surfaces typically, but not always, were in radioactive disequilibrium. Many fractures had isotopic compositions plotting near the 230Th-234U 1:1 line indicating a steady-state balance between U input and removal along with radioactive decay. Numerical simulations of U-series isotope evolution indicate that 0.5 to 1 million years are required to reach steady-state compositions. Once attained, disequilibrium 234U/238U and 230Th/238U AR values can be maintained indefinitely as long as hydrological and geochemical processes remain stable. Therefore, many Pahute Mesa fractures represent stable hydrologic pathways over million-year timescales. A smaller number of samples have non-steady-state compositions indicating transient conditions in the last several hundred thousand years. In these cases, U mobility is dominated by overall gains rather than losses of U.

Pleistocene hydrovolcanism in the Tule Lake Basin, N. E. California

DOE Office of Scientific and Technical Information (OSTI.GOV)

Lavine, A.

1993-04-01

The Prisoners Rock and The Peninsula tuff cones and the North Crater tuff ring, located in the Tule Lake Basin of northeastern California formed along a north-trending fissure approximately 270 ka when basaltic magma interacted with abundant groundwater or shallow lake water, resulting in phreatomagmatic eruptions. Diatomite inclusions in the tuff ring and correlations with the corresponding depth and diatoms in a drill core taken in the center of the basin, 2.5 km to the west of the cones, indicate shallow, marshy or shallow, alkaline-open conditions at Tule Lake around 270 ka. Deposits at Prisoners Rock and The Peninsula indicatemore » subaerial emplacement, which allowed the deposits to lithify with little erosion by the lake. Subsequent wave erosion caused undercutting and breaking off of large blocks along mainly north-trending fractures forming vertical cliff faces on the east and west sides of the cones. The cones are elongated north-south with a greater thickness of deposits on the north and northeast, probably due to prevailing southwesterly winds at the time of eruptions. Deposits of the tuff cones at Prisoners Rock and The Peninsula resulted from deep explosions caused by water-magma ratios of around 3:1. The deposits are mainly inversely graded planar surge beds, ranging in thickness from 5 to 30 cm, and grading from very fine ash to 2 cm-diameter accretionary lapilli. Emplacement by highly steam-saturated, poorly inflated pyroclastic surges is indicated by the abundance of accretionary lapilli, vesiculated tuffs, soft-sediment deformation structures, steep bedding angles (20 to 40 degrees) lack of structures beneath country rock inclusions, massive bedding, and cementation of the deposits by alteration of basaltic glass to calcite, zeolites, clays, and chlorite.« less

Isotopic and trace element variability in altered and unaltered tuffs at Yucca Mountain, Nevada

USGS Publications Warehouse

Peterman, Z.E.; Spengler, R.W.; Singer, F.R.; Dickerson, R.P.

1993-01-01

Reference stratigraphic sections near Yucca Mountain, Nevada were established and sampled in outcrop areas where the volcanic rocks have been minimally altered. Isotopic and trace element analyses obtained for these reference sections are baseline data for assessing the degree and extent of element mobility attendant with past zonal alteration of the rock mass. In agreement with earlier studies, zeolitization is shown to have occurred under wholesale open-system conditions. Calcium was increased by two three times the baseline values and strontium up to twenty times. In contrast, barium displays less variability, and the high-field strength elements zirconium and titanium were the least mobile during zeolitization. The data reported here establish the usefulness of reference sections of assessing past elements mobility. The information gained will be helpful in predicting possible future element mobility induced by thermally activated fluids in the near field of a potential repository.

Early miocene bimodal volcanism, Northern Wilson Creek Range, Lincoln County, Nevada

USGS Publications Warehouse

Willis, J.B.; Willis, G.C.

1996-01-01

Early Miocene volcanism in the northern Wilson Creek Range, Lincoln County, Nevada, produced an interfingered sequence of high-silica rhyolite (greater than 74% SiO2) ash-flow tuffs, lava flows and dikes, and mafic lava flows. Three new potassium-argon ages range from 23.9 ?? 1.0 Ma to 22.6 ?? 1.2 Ma. The rocks are similar in composition, stratigraphic character, and age to the Blawn Formation, which is found in ranges to the east and southeast in Utah, and, therefore, are herein established as a western extension of the Blawn Formation. Miocene volcanism in the northern Wilson Creek Range began with the eruption of two geochemically similar, weakly evolved ash-flow tuff cooling units. The lower unit consists of crystal-poor, loosely welded, lapilli ash-flow tuffs, herein called the tuff member of Atlanta Summit. The upper unit consists of homogeneous, crystal-rich, moderately to densely welded ash-flow tuffs, herein called the tuff member of Rosencrans Peak. This unit is as much as 300 m thick and has a minimum eruptive volume of 6.5 km3, which is unusually voluminous for tuffs in the Blawn Formation. Thick, conspicuously flow-layered rhyolite lava flows were erupted penecontemporaneously with the tuffs. The rhyolite lava flows have a range of incompatible trace element concentrations, and some of them show an unusual mixing of aphyric and porphyritic magma. Small volumes of alkaline, vesicular, mafic flows containing 50 weight percent SiO2 and 2.3 weight percent K2O were extruded near the end of the rhyolite volcanic activity. The Blawn Formation records a shift in eruptive style and magmatic composition in the northern Wilson Creek Range. The Blawn was preceded by voluminous Oligocene eruptions of dominantly calc-alkaline orogenic magmas. The Blawn and younger volcanic rocks in the area are low-volume, bimodal suites of high-silica rhyolite tuffs and lava flows and mafic lava flows.

Geology and Geochemistry of the 25.0 Ma Underdown Caldera Tuffs and tuff of Clipper Gap, Western Nevada Volcanic Field caldera belt, north-central Nevada

NASA Astrophysics Data System (ADS)

Cousens, B.; Klausen, K. B.; Henry, C.

2016-12-01

The 25.0 Ma Underdown Caldera of the Shoshone Mountains near Austin, Nevada, is part of the Ignimbrite Flare-up suite of calderas in north-central Nevada. Our goal is to characterize the geochemistry and geochronology of the tuffs, determine magma sources, and contrast Underdown with nearby contemporaneous caldera suites. The caldera is contained within a single, mildly west-tilted fault block (Bonham, 1970). The basement rocks are altered intermediate volcanic rocks, rarely intruded by rhyolite veins. The lowermost caldera unit, exposed only on the east side of the fault block, is the sparsely qtz-feld-phyric Underdown Tuff, a high-silica rhyolite (Bonham, 1970) that is columnar-jointed, densely welded, commonly includes aphyric pumice, but locally includes porphyritic pumice. Stretched pumice, flow folds, and foliations that reach nearly vertical demonstrate significant rheomorphism. A densely-welded porphyritic tuff is also present along the southeast side of the exposed caldera, and may be either blocks of an older tuff or a porphyritic phase of the Underdown Tuff. Correlative outflow, the tuff of Clipper Gap, emplaced east of the caldera, is petrographically similar with the same two pumice types. Overlying the Underdown Tuff is the Bonita Canyon Formation, which is moderately welded, commonly lithic- and pumice-rich with minor biotite, quartz and feldspar crystals, and contains reworked lenses; megabreccia of intermediate volcanic rocks and abundantly porphyritic tuff are common. This formation may be an upper part of the Underdown Tuff. On the west side of the Shoshone Mountains, the Bonita Canyon units are overlain by a more porphyritic, variably pumiceous, commonly vitrophyric, and densely welded tuff. At 24.7 Ma, this tuff is petrographically similar to and may be a younger part of the 25.2 Ma tuff of Arc Dome exposed to the east in the Toiyabe Range. Ongoing dating and geochemical analyses will constrain the timing and relationships between the tuffs.

Geochronologic and paleomagnetic evidence defining the relationship between the Miocene Hiko and Racer Canyon tuffs, eccentric outflow lobes from the Caliente caldera complex, southeastern Great Basin, USA

USGS Publications Warehouse

Gromme, S.; Deino, A.M.; Best, M.G.; Hudson, M.R.

1997-01-01

Outflow sheets of the Hiko tuff and the Racer Canyon tuff, which together extend over approximately 16000 km2 around the Caliente caldera complex in southeastern Nevada, have long been considered to be products of simultaneous or near-simultaneous eruptions from inset calderas in the west and east ends, respectively, of the caldera complex. New high-precision 40Ar/39Ar geochronology and paleomagnetic data demonstrate that emplacement of the uppermost part of the Racer Canyon tuff at 18.33??0.03 Ma was nearly synchronous with emplacement of the single outflow cooling unit of the much larger overlying Hiko tuff at 18.32??0.04 Ma. Based on comparison with the geomagnetic polarity time scale derived from the sea-floor spreading record, we conclude that emplacement of the first of several outflow cooling units of the Racer Canyon tuff commenced approximately 0.5 m.y. earlier. Only one paleomagnetic polarity is found in the Hiko tuff, but at least two paleomagnetic reversals have been found in the Racer Canyon tuff. The two formations overlap in only one place, at and near Panaca Summit northeast of the center of the Caliente caldera complex; here the Hiko tuff is stratigraphically above the Racer Canyon tuff. This study demonstrates the power of combining 40Ar/39Ar and paleomagnetic data in conjunction with phenocryst compositional modes to resolve problematic stratigraphic correlations in complex ash-flow sequences where use of one method alone might not eliminate ambiguities.

Resistance of bioparticles formed of phosphate-accumulating bacteria and zeolite to harsh environmental conditions.

PubMed

Ivankovic, Tomislav; Hrenovic, Jasna; Matonickin-Kepcija, Renata

2013-01-01

Extreme environmental conditions, such as pH fluctuations, high concentrations of toxicants or grazing of protozoa, can potentially be found in wastewater treatment systems. This study was carried out to provide specific evidence on how 'bioparticles' can resist these conditions. The term 'bioparticle' is used to describe a particle comprising natural zeolitized tuff with a developed biofilm of the phosphate-accumulating bacterial species, Acinetobacter junii, on the surface. The bacteria in the biofilm were protected from the negative influence of extremely low pH, high concentrations of benzalkonium-chloride and grazing by Paramecium caudatum and Euplotes affinis, even under conditions that caused complete eradication of planktonic bacteria. During an incubation of 24 h, the biofilms were maintained and bacteria detached from the bioparticles, thus bioaugmenting the wastewater. The bioparticles provided a safe environment for the survival of bacteria in harsh environmental conditions and could be used for successful bioaugmentation in wastewater treatment plants.

Hydrothermal Rock-Fluid Interactions in 15-year-old Submarine Basaltic Tuff at Surtsey Volcano, Iceland

NASA Astrophysics Data System (ADS)

Jackson, M. D.; Couper, S.; Li, Y.; Stan, C. V.; Tamura, N.; Stefansson, A.; Moore, J. G.; Wenk, H. R.

2016-12-01

Basaltic tephra at Surtsey volcano, produced by 1963-1967 eruptions in the offshore SE Icelandic rift zone, record the complex interplay of factors that determine rates of palagonitization and crystallization of authigenic minerals in seafloor basalts worldwide. We investigate how formation of nanocrystalline clay mineral in fresh sideromelane glass influenced crystallization of mineral cements in submarine tuff from a 181 m core drilled in 1979. Synchrotron-based microdiffraction and microfluorescence maps (2x5 µm X-ray beam spot size) at beamline 12.3.2, Advanced Light Source, SEM-EDS compositional analyses, and fluid geochemical models compare processes in lapilli-sized glass fragments, vitric cementing matrix, and fine ash accretions. In lapilli at 137.9 m (100°C), nanocrystalline clay mineral in gel-palagonite has asymetric 14.9-12.6 Å (001) reflections, with Fe and Ti enrichment relative to Si, Al and Ca, compared with adjacent sideromelane. Neighboring fibro-palagonite has symmetric (001) and greater Fe and Ti enrichment. Al-tobermorite, a rare calcium-silicate-hydrate, crystallized in nearby vesicles. The 11.30-11.49 Å (002) interlayer and Ca/(Si+Al) ratio of 0.9-1.0 record release of Si, Al, and Ca in a chemical system relatively isolated from submarine hydrothermal fluid flow. In vitric matrix relatively open to fluid flow, however, phillipsite zeolite cement predominates. Al-tobermorite formed at 88.45 m (130°C) and 102.6 m (140°C), but is associated with fibro-palagonite and analcite, reflecting more rapid palagonitization, and changing cation solubility and pH at higher temperature. Tubular palagonite microstructures show nanocrystalline clay mineral with (001) preferred orientations that wrap around relict microchannels, produced perhaps through biogenic activity. Nanocrystalline clay mineral d-spacings suggest similarities with nontronite, but zeolite in palagonite diffraction patterns and 6-9 wt% MgO suggest a polycrystalline composite with smectite mineral precursor(s). Fifteen years after eruption, Al-tobermorite-zeolite assemblages varied with porosity, pH, and reactive rock mass/liquid volume ratio in submillimeter-scale hydrothermal environments. This initial phase of alteration is rarely preserved in older palagonitized rift zone basalts.

Structure, stratigraphy, and eruption dynamics of a young tuff ring: Hanauma Bay, O'ahu, Hawai'i

NASA Astrophysics Data System (ADS)

Rottas, K. M.; Houghton, B. F.

2012-09-01

The Hanauma Bay-Koko Head complex is one of several young volcanic landforms along the Koko fissure, in southeastern O'ahu. The Hanauma Bay region of the complex comprises two nested tuff rings, inner and outer Hanauma Bay, and multiple smaller vents. The internal structure of the inner tuff ring, well exposed due to subsequent breaching by the ocean and wave erosion, indicates that it formed during a minimum of five distinct phases of deposition that produced five mappable units. Significant inward collapses generated major unconformities that separate the units exposed in the inner wall. The planes of failure are cut by narrow steep-walled, locally overhung channels and gullies, suggesting that the collapse events were each followed by short time breaks during which the deposits were eroded by rainfall runoff. Within each pyroclastic unit, there are many local slump scars and unconformities, suggesting that minor instability of the inner wall was a near-constant feature. From bedding sags and surge bed forms, it is apparent that the vent shifted at least twice during tuff ring growth. Ballistic blocks in the youngest unit indicate that the eruption overlapped in time with a separate eruption to the north, most likely to be that of the Kahauloa tuff ring 880 m away.

Task IV: Groundshock-Induced Hydrogeologic Response: Volume 2. Hydrologic Response of Deep Based Systems to Blast Loading

DTIC Science & Technology

1994-09-01

north-south. Width of the cap rock is approximately 1.5 miles, length about 3 miles and area about 4.4 square miles. According to Thordarson (1965...The volcanic tuffs making up the mesa are of moderately recent (Miocene) to very recent (Pliocene) origin. Thordarson (1965) identifies 11 layered tuff...various degrees of welded or partially welded tuff can be formed during cooling. The tuff units identified by Thordarson (1965) making up Rainier

Geochronology and correlation of Tertiary volcanic and intrusive rocks in part of the southern Toquima Range, Nye County, Nevada

USGS Publications Warehouse

Shawe, Daniel R.; Snee, Lawrence W.; Byers, Frank M.; du Bray, Edward A.

2014-01-01

Extensive volcanic and intrusive igneous activity, partly localized along regional structural zones, characterized the southern Toquima Range, Nevada, in the late Eocene, Oligocene, and Miocene. The general chronology of igneous activity has been defined previously. This major episode of Tertiary magmatism began with emplacement of a variety of intrusive rocks, followed by formation of nine major calderas and associated with voluminous extrusive and additional intrusive activity. Emplacement of volcanic eruptive and collapse megabreccias accompanied formation of some calderas. Penecontemporaneous volcanism in central Nevada resulted in deposition of distally derived outflow facies ash-flow tuff units that are interleaved in the Toquima Range with proximally derived ash-flow tuffs. Eruption of the Northumberland Tuff in the north part of the southern Toquima Range and collapse of the Northumberland caldera occurred about 32.3 million years ago. The poorly defined Corcoran Canyon caldera farther to the southeast formed following eruption of the tuff of Corcoran Canyon about 27.2 million years ago. The Big Ten Peak caldera in the south part of the southern Toquima Range Tertiary volcanic complex formed about 27 million years ago during eruption of the tuff of Big Ten Peak and associated air-fall tuffs. The inferred Ryecroft Canyon caldera formed in the south end of the Monitor Valley adjacent to the southern Toquima Range and just north of the Big Ten Peak caldera in response to eruption of the tuff of Ryecroft Canyon about 27 million years ago, and the Moores Creek caldera just south of the Northumberland caldera developed at about the same time. Eruption of the tuff of Mount Jefferson about 26.8 million years ago was accompanied by collapse of the Mount Jefferson caldera in the central part of the southern Toquima Range. An inferred caldera, mostly buried beneath alluvium of Big Smoky Valley southwest of the Mount Jefferson caldera, formed about 26.5 million years ago with eruption of the tuff of Round Mountain. The Manhattan caldera south of the Mount Jefferson caldera and northwest of the Big Ten Peak caldera formed in association with eruption of a series of tuffs, principally the Round Rock Formation, mostly ash-flow tuff, about 24.4 million years ago. Extensive 40Ar/39Ar dating of about 60 samples that represent many of the Tertiary extrusive and intrusive rocks in the southern Toquima Range provides precise ages that refine the chronology of previously dated units. New geochronologic data indicate that the petrogenetically related Corcoran Canyon, Ryecroft Canyon, and Mount Jefferson calderas formed during a period of about 560,000 years. Electron microprobe analyses of phenocrysts from 20 samples of six dated units underscore inferred petrogenetic relations among some of these units. In particular, compositions of augite, hornblende, and biotite in tuffs erupted from the Corcoran Canyon, Ryecroft Canyon, and Mount Jefferson calderas are similar, which suggests that magmas represented by these tuffs have similar petrogenetic histories. The unique occurrence of hypersthene in Isom-type tuff confirms its derivation from a source beyond the southern Toquima Range.

Surface complexation modeling of americium sorption onto volcanic tuff.

PubMed

Ding, M; Kelkar, S; Meijer, A

2014-10-01

Results of a surface complexation model (SCM) for americium sorption on volcanic rocks (devitrified and zeolitic tuff) are presented. The model was developed using PHREEQC and based on laboratory data for americium sorption on quartz. Available data for sorption of americium on quartz as a function of pH in dilute groundwater can be modeled with two surface reactions involving an americium sulfate and an americium carbonate complex. It was assumed in applying the model to volcanic rocks from Yucca Mountain, that the surface properties of volcanic rocks can be represented by a quartz surface. Using groundwaters compositionally representative of Yucca Mountain, americium sorption distribution coefficient (Kd, L/Kg) values were calculated as function of pH. These Kd values are close to the experimentally determined Kd values for americium sorption on volcanic rocks, decreasing with increasing pH in the pH range from 7 to 9. The surface complexation constants, derived in this study, allow prediction of sorption of americium in a natural complex system, taking into account the inherent uncertainty associated with geochemical conditions that occur along transport pathways. Published by Elsevier Ltd.

Woolly erionite from the Reese River zeolite deposit, Lander County, Nevada, and its relationship to other erionites

USGS Publications Warehouse

Gude, Arthur J.; Sheppard, Richard A.

1981-01-01

Woolly erionite from the Reese River deposit, Nevada, is identical in appearance to that at the type locality, near Durkee, Oregon. Both of these erionites differ in appearance from all other erionite reported in the past 20 years from diverse rocks throughout the world which are described as prismatic or acicular in habit. The non-woolly erionites are especially common as microscopic crystals in diagenetically altered vitroclastic lacustrine deposits of Cenozoic age. The Reese River woolly erionite fills joints in gray to brownish-gray lacustrine mudstone of probably Pliocene age, in a zone about 1 m thick beneath a conspicuous gray vitric tuff. Compact masses of long, curly, woolly erionite fibers are in the plane of the joint and locally are associated with opal. Indices of refraction are ω = 1.468 and ε = 1.472; hexagonal unit-cell parameters are a = 13.186(2) Å, c = 15.055(1) Å, and V = 2267.1(0.9) Å3. A chemical analysis of woolly erionite yields a unit-cell composition of: Na1.01K2.84Mg0.3Ca1.69Al8.18Si27.84O72 · 28.51H2O.

Correlation of the KHS Tuff of the Kibish Formation to volcanic ash layers at other sites, and the age of early Homo sapiens (Omo I and Omo II).

PubMed

Brown, Francis H; McDougall, Ian; Fleagle, John G

2012-10-01

Hominin specimens Omo I and Omo II from Member I of the Kibish Formation, Ethiopia are attributed to early Homo sapiens, and an age near 196 ka has been suggested for them. The KHS Tuff, within Member II of the Kibish Formation has not been directly dated at the site, but it is believed to have been deposited at or near the time of formation of sapropel S6 in the Mediterranean Sea. Electron microprobe analyses suggest that the KHS Tuff correlates with the WAVT (Waidedo Vitric Tuff) at Herto, Gona, and Konso (sample TA-55), and with Unit D at Kulkuletti in the Ethiopian Rift Valley. Konso sample TA-55 is older than 154 ka, and Unit D at Kulkuletti is dated at 183 ka. These correlations and ages provide strong support for the age originally suggested for the hominin remains Omo I and Omo II, and for correlation of times of deposition in the Kibish region with formation of sapropels in the Mediterranean Sea. The Aliyo Tuff in Member III of the Kibish Formation is dated at 104 ka, and correlates with Gademotta Unit 15 in the Ethiopian Rift Valley. Copyright © 2012 Elsevier Ltd. All rights reserved.

Geochronology of the mammal-bearing late Cenozoic on the northern Altiplano, Bolivia

NASA Astrophysics Data System (ADS)

Marshall, L. G.; Swisher, C. C.; Lavenu, A.; Hoffstetter, R.; Curtis, G. H.

1992-01-01

Samples of seven tuff or ignimbrite units associated with known land mammal faunas of late Miocene and Pliocene age were collected from 17 localities on the northern Altiplano of western Bolivia. Mineral separates dated by the classic 40K- 40Ar technique (35 dates) and by single crystal laser fusion (SCLF) 40Ar/ 39Ar analysis (84 dates) indicate the following preferred ages based on SCLF 40Ar/ 39Ar dates on sanidine for six of these units: Ulloma Tuff, 10.35±0.06 Ma; Callapa Tuff, 9.03±0.07 Ma; Toba 76, 5.348±0.003 Ma; Ayo Ayo Tuff, 2.896±0.006 Ma; Perez Ignimbrite, 2.815±0.005 Ma; and Chijini Tuff, 2.650±0.012 Ma. Land mammal faunas of early Huayquerian age are bracketed below by the Callapa Tuff (9.0 Ma) and above the base of the Cerke Formation (7.6 Ma); faunas of Montehermosan age are bracketed below by the Toba 76 and Cota Cota Tuffs ( ca. 5.4 Ma), and above by the Ayo Ayo and Chijini Tuffs ( ca. 2.8 Ma) of the Umala and La Paz Formations, respectively; and faunas of Ensenadan and Lujanian age occur in rocks younger than 1.6 Ma. Hiatuses identified by the absence of late Huayquerian and Chapadmalalan-Uquian faunas correlate with unconformities which are interpreted as deformation phases: the first with Q3 (8.0-5.5 Ma) and the second with Q4 (2.8-1.6 Ma) of the Quechua Orogeny.

High-temperature, large-volume, lavalike ash-flow tuffs without calderas in southwestern Idaho

USGS Publications Warehouse

Ekren, E.B.; McIntyre, David H.; Bennett, Earl H.

1984-01-01

Rhyolitic rocks were erupted from vents in and adjacent to the Owyhee Mountains and Owyhee Plateau of southwestern Idaho from 16 m.y. ago to about 10 m.y. ago. They were deposited on a highly irregular surface developed on a variety of basement rocks that include granitic rocks of Cretaceous age, quartz latite and rhyodacite tuffs and lava flows of Eocene age, andesitic and basaltic lava flows of Oligocene age, and latitic and basaltic lava flows of early Miocene age. The rhyolitic rocks are principally welded tuffs that, regardless of their source, have one feature in common-namely internal characteristics indicating en-masse, viscous lavalike flowage. The flowage features commonly include considerable thicknesses of flow breccia at the bases of various cooling units. On the basis of the tabular nature of the rhyolitic deposits, their broad areal extents, and the local preservation of pyroclastic textures at the bases, tops, and distal ends of some of the deposits, we have concluded that the rocks were emplaced as ash flows at extremely high temperatures and that they coalesced to liquids before final emplacement and cooling. Temperatures of l090?C and higher are indicated by iron-titanium oxide compositions. Rhyolites that are about 16 m.y. old are preserved mostly in the downdropped eastern and western flanks of the Silver City Range and they are inferred to have been erupted from the Silver City Range. They rarely contain more than about 2 percent phenocrysts that consist of quartz and subequal amounts of plagioclase and alkali feldspar; commonly, they contain biotite, and they are the only rhyolitic rocks in the area to do so. The several rhyolitic units that are 14 m.y. to about 10 m.y. old contain only pyroxene-principally ferriferous and intermediate pigeonites-as mafic constituents. The rhyolites of the Silver City Range comprise many cooling units, none of which can be traced for great distances. Rocks erupted from the Owyhee Plateau include two sequences that were traced over areas having diameters of about 100 km. These two sheets are the herein-named Swisher Mountain Tuff, which is about 13.8 m.y. old, and the Little Jacks Tuff, which is about 10 m.y. old. The Swisher Mountain Tuff was erupted from the Juniper Mountain volcanic center, a gentle dome that is not bounded by arcuate faults indicative of cauldron subsidence. The tuff is 200 m thick over a considerable area in and adjacent to its source. It apparently thins gradually toward its distal edges, and it is inferred to be uniformly distributed around its source at Juniper Mountain. The unit contains vitrophyres at various intervals from base to top, and, although the vitrophyres are, in general, flow layered and commonly flow brecciated, they occasionally contain well-defined pumice clasts. The vitrophyres indicate compound cooling, and, near the distal edges of the sheet, some of them probably represent complete cooling breaks. The Little Jacks Tuff onlaps the Swisher Mountain Tuff in expo sures east of Juniper Mountain, and it is inferred to have been erupted from a source on the part of the Owyhee Plateau that lies just east of the area studied. This inferred source area, like that at Juniper Mountain, is also expressed today as a gentle dome without structural features indicative of cauldron subsidence. The Little Jacks Tuff, in most exposures in the deep canyons of the Plateau, consists of at least four cooling units, and, in places in the eastern part of the studied area near the source area, it possibly comprises as many as six. Although there is no obvious evidence of erosion between the various cooling units, magnetic polarity measurements indicate that there were at least two magnetic reversals during the eruption interval of the Little Jacks Tuff. Like the Swisher Mountain Tuff, the Little Jacks has flattened pumice clasts in a few outcrops-principally at the bases of the various cooling units. The two tuff sequences are calc-a

Mineralogy and sedimentology of the Miocene Göcenoluk borate deposit, Kırka district, western Anatolia, Turkey

NASA Astrophysics Data System (ADS)

García-Veigas, Javier; Helvacı, Cahit

2013-05-01

The Miocene boratiferous district of Kırka, in western Anatolia (Turkey), is the most important Na-borate (borax) resource in the world. Two separate deposits in the Kırka district are located near the villages of Sarıkaya and Göcenoluk (Eskişehir Province). Borax is intensively exploited in open-pit mines in the Sarıkaya deposit while only small quarries of colemanite are known in the Göcenoluk deposit. Recent exploratory drilling in the Göcenoluk area intersected a thick succession of dolostones, tuffs and three borate-bearing units (Lower, Intermediate and Upper Borate Units). In them, the most abundant borate mineral is ulexite (Ca-Na-borate) passing at depth to probertite. Borax (Na-borate) is only present in the Intermediate Borate Unit. Minor amounts of colemanite (Ca-borate) and hydroboracite (Ca-Mg-borate) occur at the base, and/or top, of each mineralized unit. Pyroclastic layers within the borate units show intense alteration by alkaline, boron-bearing waters and formation of diagenetic clay minerals (smectites), zeolites (analcime) and borosilicates (searlesite). The Göcenoluk succession is interpreted as a shallow, ephemeral, alkaline lake deposit in which carbonates formed as stromatolites and travertines. Borate precipitation in the Göcenoluk area took place interstitially within muddy and carbonate sediments in a lateral progression from marginal Ca-borates towards Na-Ca-borates and rarely to Na-borates in the center of the lake. Authigenic silicate mineral distribution shows parallel changes toward the center of the lake that reflect increasing pH gradient.

Building zeolites from pre-crystallized units: nanoscale architecture.

PubMed

Corma, Avelino; Li, Chengeng; Moliner, Manuel

2018-01-24

Since the earlier descriptions by Barrer in the 40's on converting natural minerals into synthetic zeolites, the use of pre-crystallized zeolites as crucial inorganic directing agents to synthesize other crystalline zeolites with improved physico-chemical properties, has become a very intense and relevant research field, allowing the design, particularly in the last years, of new industrial catalysts. In the present review, we will highlight how the presence of some crystalline fragments in the synthesis media, such as small secondary building units (SBUs) or layered substructures, not only favors the crystallization of other zeolites presenting similar SBUs or layers, but also permits mostly controlling important parameters affecting to their catalytic activity (i.e. chemical composition, crystal size, or porosity, among others). In this sense, the recent advances on the preparation of 3-D and 2-D related zeolites through seeding and zeolite-to-zeolite transformation processes will be extensively revised, including their preparation in presence or absence of organic structure directing agents (OSDAs), with the aim of introducing general guidelines for designing more efficient future synthesis approaches for target zeolites. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

A Hierarchical MFI Zeolite with a Two-Dimensional Square Mesostructure.

PubMed

Shen, Xuefeng; Mao, Wenting; Ma, Yanhang; Xu, Dongdong; Wu, Peng; Terasaki, Osamu; Han, Lu; Che, Shunai

2018-01-15

A conceptual design and synthesis of ordered mesoporous zeolites is a challenging research subject in material science. Several seminal articles report that one-dimensional (1D) mesostructured lamellar zeolites are possibly directed by sheet-assembly of surfactants, which collapse after removal of intercalated surfactants. However, except for one example of two-dimensional (2D) hexagonal mesoporous zeolite, no other zeolites with ordered 2D or three-dimensional (3D) mesostructures have been reported. An ordered 2D mesoporous zeolite can be templated by a cylindrical assembly unit with specific interactions in the hydrophobic part. A template molecule with azobenzene in the hydrophobic tail and diquaternary ammonium in the hydrophilic head group directs hierarchical MFI zeolite with a 2D square mesostructure. The material has an elongated octahedral morphology, and quaternary, ordered, straight, square channels framed by MFI thin sheets expanded along the a-c planes and joined with 90° rotations. The structural matching between the cylindrical assembly unit and zeolite framework is crucial for mesostructure construction. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Geohydrologic data from test hole USW UZ-7, Yucca Mountain area, Nye County, Nevada

USGS Publications Warehouse

Kume, Jack; Hammermeister, D.P.

1990-01-01

This report contains a description of the methods used in drilling and coring of the test-hole USW UZ-7, a description of the methods used in collecting, handling, and testing of test-hole samples; Lithologic information from the test hole; and water-content, water-potential, bulk-density, grain-density, porosity, and tritium data for the test hole. Test-hole USW UZ-7 was drilled and cored to a total depth of 62.94 m. The drilling was done using air as a drilling fluid to minimize disturbance to the water content of cores, drill-bit cuttings, and borehole wall-rock. Beginning at the land surface, the unsaturated-zone rock that was penetrated consisted of alluvium; welded and partially to nonwelded ash-flow tuff; bedded and reworked ash-fall tuff; nonwelded ash-flow tuff; and welded ash-flow tuff. Values of gravimetric water content and water potential of alluvium were intermediate between the extreme values in welded and nonwelded units of tuff. Gravimetric water content was largest in bedded and nonwelded ash-fall tuffs and was smallest in welded ash-flow tuff. Values of water potential were more negative in densely welded ash-flow tuffs and were less negative in bedded and nonwelded ash-fall tuffs. Bulk density was largest in densely welded ash-flow tuffs and smallest in nonwelded and bedded ash-fall tuffs. Grain density was uniform but was slightly larger in nonwelded and bedded ash-fall tuffs than in welded ash-flow tuffs. Porosity trends were opposite to bulk-density trends. Tritium content in alluvium was smallest near the alluvium-bedrock contact, markedly increased in the middle of the deposit, and decreased in the near-surface zone of the deposit. (Author 's abstract)

The geology and chronology of the Acheulean deposits in the Mieso area (East-Central Ethiopia).

PubMed

Benito-Calvo, Alfonso; Barfod, Dan N; McHenry, Lindsay J; de la Torre, Ignacio

2014-11-01

This paper presents the Quaternary sequence of the Mieso area of Central-East Ethiopia, located in the piedmont between the SE Ethiopian Escarpment and the Main Ethiopian Rift-Afar Rift transition sector.In this region, a piedmont alluvial plain is terraced at þ25 m above the two main fluvial courses, the Mieso and Yabdo Rivers. The piedmont sedimentary sequence is divided into three stratigraphic units separated by unconformities. Mieso Units I and II contain late Acheulean assemblages and a weakly consolidated alluvial sequence, consisting mainly of fine sediments with buried soils and, to a lesser degree, conglomerates. Palaeo-wetland areas were common in the alluvial plain, represented by patches of tufas, stromatolites and clays. At present, the piedmont alluvial surface is preserved mainly on a dark brown soil formed at the top of Unit II. Unit III corresponds to a fluvial deposit overlying Unit II, and is defined by sands, silty clays and gravels, including several Later Stone Age (LSA) occurrences. Three fine-grained tephra levels are interbedded in Unit I (tuffs TBI and TA) and II (tuff CB), and are usually spatially-constrained and reworked. Argon/argon (40Ar/39Ar) dating from tuff TA, an ash deposit preserved in a palustrine environment, yielded an age of 0.212 ± 0.016 Ma (millions of years ago). This date places thetop of Unit I in the late Middle Pleistocene, with Acheulean sites below and above tuff TA. Regional correlations tentatively place the base of Unit I around the Early-Middle Pleistocene boundary, Unit II inthe late Middle Pleistocene and within the Late Pleistocene, and the LSA occurrences of Unit III in the LatePleistoceneeHolocene.

Influence of Crystal Expansion/Contraction on Zeolite Membrane Permeation

DOE Office of Scientific and Technical Information (OSTI.GOV)

Sorenson, Stephanie G; Payzant, E Andrew; Noble, Richard D

X-ray diffraction was used to measure the unit cell parameters of B-ZSM-5, SAPO-34, and NaA zeolite powders as a function of adsorbate loading at 303 K, and in one case, at elevated temperatures. Most adsorbates expanded the zeolite crystals below saturation loading at 303 K: n-hexane and SF6 in B-ZSM-5, methanol and CO2 in SAPO-34, and methanol in NaA zeolite. As the loadings increased, the crystals expanded more. Changes in the unit cell volumes of B-ZSM-5 and SAPO-34 zeolite powders correlated with changes in permeation through zeolite membranes defects. When the zeolite crystals expanded or contracted upon adsorption, the defectmore » sizes decreased or increased. In B-ZSM-5 membranes, the fluxes through defects decreased dramatically when n-hexane or SF6 adsorbed. In contrast, i-butane adsorption at 303 K contracted B-ZSM-5 crystals at low loadings and expanded them at higher loadings. Correspondingly, the flux through B-ZSM-5 membrane defects increased at low i-butane loadings and decreased at high loading because the defects increased in size at low loading and decreased at high loadings. At 398 K and 473 K, n-hexane expanded the B-ZSM-5 unit cell more as the temperature increased from 303 to 473 K. The silicalite-1 and B-ZSM-5 unit cell volumes expanded similarly upon n-hexane adsorption at 303 K; boron substitution had little effect on volume expansion.« less

Volcanotectonic history of Crater Flat, southwestern Nevada, as suggested by new evidence from drill hole USW-VH-1 and vicinity

USGS Publications Warehouse

Carr, W.J.

1982-01-01

New evidence for a possible resurgent dome in the caldera related to eruption of the Bullfrog Member of the Crater Flat Tuff has been provided by recent drilling of a 762-meter (2,501-foot) hole in central Crater Flat. Although no new volcanic units were penetrated by the drill hole (USW-VH-1), the positive aeromagnetic anomaly in the vicinity of the drill hole appears to result in part from the unusually thick, densely welded tuff of the Bullfrog. Major units penetrated include alluvium, basalt of Crater Flat, Tiva Canyon and Topopah Spring Members of the Paintbrush Tuff, and Prow Pass and Bullfrog Members of the Crater Flat Tuff. In addition, the drill hole provided the first subsurface hydrologic information for the area. The water table in the hole is at about 180 meters (600 feet), and the temperature gradient appears slightly higher than normal for the region.

Mapping of hydrothermally altered rocks using airborne multispectral scanner data, Marysvale, Utah, mining district

USGS Publications Warehouse

Podwysocki, M.H.; Segal, D.B.; Jones, O.D.

1983-01-01

Multispectral data covering an area near Marysvale, Utah, collected with the airborne National Aeronautics and Space Administration (NASA) 24-channel Bendix multispectral scanner, were analyzed to detect areas of hydrothermally altered, potentially mineralized rocks. Spectral bands were selected for analysis that approximate those of the Landsat 4 Thematic Mapper and which are diagnostic of the presence of hydrothermally derived products. Hydrothermally altered rocks, particularly volcanic rocks affected by solutions rich in sulfuric acid, are commonly characterized by concentrations of argillic minerals such as alunite and kaolinite. These minerals are important for identifying hydrothermally altered rocks in multispectral images because they have intense absorption bands centered near a wavelength of 2.2 ??m. Unaltered volcanic rocks commonly do not contain these minerals and hence do not have the absorption bands. A color-composite image was constructed using the following spectral band ratios: 1.6??m/2.2??m, 1.6??m/0.48??m, and 0.67??m/1.0??m. The particular bands were chosen to emphasize the spectral contrasts that exist for argillic versus non-argillic rocks, limonitic versus nonlimonitic rocks, and rocks versus vegetation, respectively. The color-ratio composite successfully distinguished most types of altered rocks from unaltered rocks. Some previously unrecognized areas of hydrothermal alteration were mapped. The altered rocks included those having high alunite and/or kaolinite content, siliceous rocks containing some kaolinite, and ash-fall tuffs containing zeolitic minerals. The color-ratio-composite image allowed further division of these rocks into limonitic and nonlimonitic phases. The image did not allow separation of highly siliceous or hematitically altered rocks containing no clays or alunite from unaltered rocks. A color-coded density slice image of the 1.6??m/2.2??m band ratio allowed further discrimination among the altered units. Areas containing zeolites and some ash-fall tuffs containing montmorillonite were readily recognized on the color-coded density slice as having less intense 2.2-??m absorption than areas of highly altered rocks. The areas of most intense absorption, as depicted in the color-coded density slice, are dominated by highly altered rocks containing large amounts of alunite and kaolinite. These areas form an annulus, approximately 10 km in diameter, which surrounds a quartz monzonite intrusive body of Miocene age. The patterns of most intense alteration are interpreted as the remnants of paleohydrothermal convective cells set into motion during the emplacement of the central intrusive body. ?? 1983.

Contrasting perspectives on the Lava Creek Tuff eruption, Yellowstone, from new U–Pb and 40Ar/39Ar age determinations

USGS Publications Warehouse

Wilson, Colin J. N.; Stelten, Mark; Lowenstern, Jacob B.

2018-01-01

The youngest major caldera-forming event at Yellowstone was the ~ 630-ka eruption of the Lava Creek Tuff. The tuff as mapped consists of two major ignimbrite packages (members A and B), linked to widespread coeval fall deposits and formation of the Yellowstone Caldera. Subsequent activity included emplacement of numerous rhyolite flows and domes, and development of two structurally resurgent domes (Mallard Lake and Sour Creek) that accommodate strain due to continual uplift/subsidence cycles. Uplifted lithologies previously mapped on and adjacent to Sour Creek dome were thought to include the ~ 2.08-Ma Huckleberry Ridge Tuff, cropping out beneath Lava Creek Tuff members A and B. Mapped outcrops of this Huckleberry Ridge Tuff material were sampled as welded ignimbrite (sample YR345) on Sour Creek dome, and at nearby Bog Creek as welded ignimbrite (YR311) underlain by an indurated lithic lag breccia containing blocks of another welded ignimbrite (YR324). Zircon near-rim U–Pb analyses from these samples yield weighted mean ages of 661 ± 13 ka (YR345: 95% confidence), 655 ± 11 ka (YR311), and 664 ± 15 ka (YR324) (combined weighted mean of 658.8 ± 6.6 ka). We also studied two samples of ignimbrite previously mapped as Huckleberry Ridge Tuff on the northeastern perimeter of the Yellowstone Caldera, ~ 12 km ENE of Sour Creek dome. Sanidines from these samples yield 40Ar/39Ar age estimates of 634.5 ± 6.8 ka (8YC-358) and 630.9 ± 4.1 ka (8YC-359). These age data show that all these units represent previously unrecognized parts of the Lava Creek Tuff and do not have any relationship to the Huckleberry Ridge Tuff. Our observations and data imply that the Lava Creek eruption was more complex than is currently assumed, incorporating two tuff units additional to those currently mapped, and which themselves are separated by a time break sufficient for cooling and some reworking. The presence of a lag breccia suggests that a source vent lay nearby (< ~ 3 km) for some of the tuffs and that the Yellowstone Caldera boundary in this area could be reconsidered.

Contrasting perspectives on the Lava Creek Tuff eruption, Yellowstone, from new U-Pb and 40Ar/39Ar age determinations

NASA Astrophysics Data System (ADS)

Wilson, Colin J. N.; Stelten, Mark E.; Lowenstern, Jacob B.

2018-06-01

The youngest major caldera-forming event at Yellowstone was the 630-ka eruption of the Lava Creek Tuff. The tuff as mapped consists of two major ignimbrite packages (members A and B), linked to widespread coeval fall deposits and formation of the Yellowstone Caldera. Subsequent activity included emplacement of numerous rhyolite flows and domes, and development of two structurally resurgent domes (Mallard Lake and Sour Creek) that accommodate strain due to continual uplift/subsidence cycles. Uplifted lithologies previously mapped on and adjacent to Sour Creek dome were thought to include the 2.08-Ma Huckleberry Ridge Tuff, cropping out beneath Lava Creek Tuff members A and B. Mapped outcrops of this Huckleberry Ridge Tuff material were sampled as welded ignimbrite (sample YR345) on Sour Creek dome, and at nearby Bog Creek as welded ignimbrite (YR311) underlain by an indurated lithic lag breccia containing blocks of another welded ignimbrite (YR324). Zircon near-rim U-Pb analyses from these samples yield weighted mean ages of 661 ± 13 ka (YR345: 95% confidence), 655 ± 11 ka (YR311), and 664 ± 15 ka (YR324) (combined weighted mean of 658.8 ± 6.6 ka). We also studied two samples of ignimbrite previously mapped as Huckleberry Ridge Tuff on the northeastern perimeter of the Yellowstone Caldera, 12 km ENE of Sour Creek dome. Sanidines from these samples yield 40Ar/39Ar age estimates of 634.5 ± 6.8 ka (8YC-358) and 630.9 ± 4.1 ka (8YC-359). These age data show that all these units represent previously unrecognized parts of the Lava Creek Tuff and do not have any relationship to the Huckleberry Ridge Tuff. Our observations and data imply that the Lava Creek eruption was more complex than is currently assumed, incorporating two tuff units additional to those currently mapped, and which themselves are separated by a time break sufficient for cooling and some reworking. The presence of a lag breccia suggests that a source vent lay nearby (< 3 km) for some of the tuffs and that the Yellowstone Caldera boundary in this area could be reconsidered.

Diatreme evolution during the phreatomagmatic eruption of the Songaksan tuff ring, Jeju Island, Korea

NASA Astrophysics Data System (ADS)

Go, S. Y.; Kim, G. B.; Jeong, J. O.; Sohn, Y. K.

2017-03-01

The Songaksan tuff ring, Jeju Island, Korea, which erupted ca. 3.7 ka BP in a coastal setting, provides an unusual opportunity to study the processes of phreatomagmatic eruption and the formation of a diatreme because of the exceptionally well-preserved ejecta beds and well-known subsurface geology. The tuff sequence can be divided into four units (A to D), which have distinctly different accidental componentry (quartz-rich vs. quartz-poor), grain surface features (abraded and ash-coated vs. unabraded and uncoated), and chemical compositions of juvenile particles. The basal tephra bed of unit A, which probably erupted after the removal of the relatively hard shallow-level (<120 m deep) substrate by initial cratering, comprises only unabraded and uncoated grains and contains abundant relatively deep-derived (>120 m deep) accidental grains, suggesting that the early erupted tephra had not yet experienced recycling and pre-eruption mixing in the diatreme. On the other hand, the overlying tephra beds of units A, B, and D contain an abundance of abraded and ash-coated juvenile/accidental grains, suggesting that the tephra comprised significant proportions of "recycled" or "premixed" materials from previous eruptions or subsurface explosions, which participated in the explosion-driven mixing in the diatreme before eventual ejection from the diatreme. Unit C is unusual in that it comprises extremely rare accidental grains and ash-coated juvenile/accidental grains. We interpret that the supply of solid materials, either accidental or juvenile, to the diatreme was greatly reduced because of temporary stabilization of the diatreme and the reduction in magma flux to the diatreme. The diatreme is therefore envisaged to have been filled with a water-saturated slurry, in which particle abrasion and adhesion were inhibited. We also infer that the diatreme fill was temporarily removed by a powerful explosion before eruption of unit C on the basis of the near absence of the tephra grains from earlier eruptions throughout the tephra beds of unit C. The ratio of tachylite to sideromelane grains generally increases up-section of the tuff sequence with two abrupt drops across the tuff unit boundaries. These variations are coincident with the changes in the chemical composition of juvenile particles, suggesting an overall decrease in magma flux punctuated by brief increases in magma flux associated with the arrival of new magma batches. The textural and compositional variations of the Songaksan tuff ring suggest that there can be significant variability in diatreme processes even during a purely phreatomagmatic eruption of a tuff ring, including removal and renewal of the diatreme fill, and that there is still much room for further investigation of the diatreme processes from the ejecta beds in order to make the current diatreme model more robust.

Petrology and geochemistry of the Grouse Canyon Member of the Belted Range Tuff, Rock-Mechanics Drift, U12g Tunnel, Nevada Test Site

DOE Office of Scientific and Technical Information (OSTI.GOV)

Connolly, J.R.; Mansker, W.L.; Hicks, R.

1983-04-01

G-Tunnel at Nevada Test Site (NTS) is the site of thermal and thermomechanical experiments examining the feasibility of emplacing heat-producing nuclear wastes in silicic tuffs. This report describes the general stratigraphy, mineralogy, and bulk chemistry of welded portions of the Grouse Canyon Member of the Belted Range Tuff, the unit in which most of these experiments will be performed. The geologic characteristics of the Grouse Canyon Member are compared with those of the Topopah Spring Member of the Paintbrush Tuff, presently the preferred horizon for an actual waste repository at Yucca Mountain, near the southwest boundary of Nevada Test Site.more » This comparison suggests that test results obtained in welded tuff from G-Tunnel are applicable, with limitations, to evaluation of the Topopah Spring Member at Yucca Mountain.« less

Petrologic evolution of the Caetano magmatic system: What can we learn from a dissected, 34 Ma caldera in the northern Great Basin, western U.S.A.?

NASA Astrophysics Data System (ADS)

Watts, K. E.; Colgan, J. P.; John, D. A.; Henry, C. D.

2012-12-01

Eruption of the >1,100 km3 Caetano Tuff and formation of the Caetano caldera occurred during the mid-Tertiary ignimbrite flare-up in the Great Basin. Post-collapse extension and faulting created a series of tilted fault blocks that expose >4 km thick intracaldera tuff, two generations of resurgent granitic plutons, silicic ring-fracture intrusions, a tuff dike that fed the early eruption, and pre- and post-caldera andesites. We integrate new petrologic data for extrusive and intrusive Caetano units with geologic mapping and geochronology to provide an exceptional view into the inner workings of a large caldera center. The Caetano Tuff is a phenocryst-rich (~30-50%) ignimbrite with a mineralogy of plagioclase + sanidine + quartz + biotite + orthopyroxene + Fe-Ti oxides ± hornblende + accessory zircon and allanite. Plagioclase crystals in the Caetano Tuff and cogenetic intrusive units span a wide compositional range (>30 mol% An) and have diverse petrographic textures ranging from euhedral phenocrysts to anhedral, sieved crystals with melt-rich cores. Plagioclase compositions measured by electron microprobe for whole rock thin sections are consistent with compositional zoning of the intracaldera tuff shown by XRF whole rock analyses, oligoclase (~10-30 mol% An) and andesine (~30-50 mol% An) in the most evolved (75-77% SiO2) and least evolved (72-74% SiO2) tuff units, respectively. However, orthopyroxene compositions are apparently decoupled from the host tuff composition, with the highest Mg#s (~60-70%) occurring in the most evolved tuff samples. In the Caetano Tuff, equilibrium pairs of Fe-Ti oxides yield an average eruption temperature of 745°C, which is consistent with the average Ti-in-zircon temperature of 750±70°C (1 stdev, n=90 spots) obtained from Ti concentrations measured by SHRIMP for single zircons. Application of Al-in-hornblende geobarometry indicates an average equilibration pressure of 4.5±0.1 kbar, corresponding to mid-crustal magma storage depths of ~14-15 km. In light of our new petrologic data, we highlight the following key points: (1) Diverse crystal cargoes, disequilibrium textures, and wide compositional oscillations in single phenocrysts and among discrete mineral populations indicate prolonged and complex episodes of magma assembly and growth. Based on zircon U-Pb SHRIMP ages that range from ~34-37 Ma, assembly and growth may have spanned ~2-3 Ma, or a 34 Ma Caetano magma chamber may have assimilated older igneous rocks in and around the caldera. (2) Mineral chemistry, U-Pb and Ar-Ar geochronology, O isotope geochemistry, and whole rock major and trace element geochemistry indicate a genetic connection between the Caetano Tuff and resurgent granitic plutons, supporting the role of linked volcanic-plutonic components in caldera settings. (3) Generation and eruption of crystal-rich "monotonous" rhyolite calls into question the prevailing paradigms of crystal-poor rhyolites derived from crystal mushes, or crystal-rich "monotonous intermediates" derived from homogeneous dacitic magma reservoirs. The Caetano Tuff may be a representative end member of caldera-forming eruptions that is important for understanding large-volume rhyolite genesis in the shallow-middle crust.

Records of Triassic volcanism in Pangean Great Lakes, and implications for reconstructing the distal effects of Large Igneous Provinces

NASA Astrophysics Data System (ADS)

Whiteside, J. H.; Percival, L.; Kinney, S.; Olsen, P. E.; Mather, T. A.; Philpotts, A.

2017-12-01

Documentation of the precise timing of volcanic eruptions in sedimentary records is key for linking volcanic activity to both historical and geological episodes of environmental change. Deposition of tuffs in sediments, and sedimentary enrichment of trace metals linked to igneous processes, are both commonly used for such correlations. In particular, sedimentary mercury (Hg) enrichments have been used as a marker for volcanic activity from Large Igneous Provinces (LIPs) to support their link to episodes of major climate change and mass extinction in the geological record. However, linking such enrichments to a specific eruption or eruption products is often challenging or impossible. In this study, the mercury records from two exactly contemporaneous latest Triassic-earliest Jurassic rift lakes are presented. Both sedimentary records feature igneous units proposed to be related to the later (Early Jurassic) stages of volcanism of the Central Atlantic Magmatic Province (CAMP). These CAMP units include a small tuff unit identified by thin-section petrology and identified at 10 localities over a distance of over 200 km, and a major CAMP basalt flow overlying this tuff (and dated at 200.916±0.064 Ma) which is also known across multiple sedimentary basins in both North America and Morocco and is thought to have been emplaced about 120 kyr after the tuff. A potential stratigraphic correlation between Hg enrichments and the igneous units is considered, and compared to the established records of mercury enrichments from the latest Triassic that are thought to be coeval with the earlier stages of CAMP volcanism. Investigating the Hg records of sedimentary successions containing tuffs and basalt units is an important step for demonstrating whether the mercury emissions from specific individual volcanic eruptions in the deep past can be identified in the geological record, and are thus important tools for interpreting the causes of associated past geological events, such as mass extinctions.

Simple approach in understanding interzeolite transformations using ring building units

NASA Astrophysics Data System (ADS)

Suhendar, D.; Buchari; Mukti, R. R.; Ismunandar

2018-04-01

Recently, there are two general approaches used in understanding interzeolite transformations, thermodynamically represented by framework density (FD) and kinetically by structural building units. Two types of structural building units are composite building units (CBU’s) and secondary building units (SBU’s). This study aims to examine the approaches by using interzeolite transformation data available in literature and propose a possible alternative approach. From a number of cases of zeolite transformation, the FD and CBU approach are not suitable for use. The FD approach fails in cases involving zeolite parents that have moderate or high FD’s, while CBU approach fails because of CBU’s unavailability in parent zeolites compared with CBU’s in their transformation products. The SBU approach is most likely to fit because SBU’s are units that have basic form of ring structures and closer to the state and shape of oligomeric fragments present in zeolite synthesis or dissolution cases. Thus, a new approach can be considered in understanding the interzeolite transformation, namely the ring building unit (RBU) approach. The advantage of RBU approach is RBU’s can be easily derived from all framework types, but in SBU approach there are several types of frameworks that cannot be expressed in SBU forms.

Deep Vadose Zone Flow and Transport Behavior at T-Tunnel Complex, Rainier Mesa, Nevada National Security Site

NASA Astrophysics Data System (ADS)

Parashar, R.; Reeves, D. M.

2010-12-01

Rainier Mesa, a tuffaceous plateau on the Nevada National Security Site, has been the location of numerous subsurface nuclear tests conducted in a series of tunnel complexes located approximately 450 m below the top of the mesa and 500 m above the regional groundwater flow system. The tunnels were constructed near the middle of an 800 m Tertiary sequence of faulted, low-permeability welded and non-welded bedded, vitric, and zeolitized tuff units. Water levels from wells in the vicinity of the T-tunnel complex indicate the presence of a perched saturation zone located approximately 100 m above the T-tunnel complex. This upper zone of saturation extends downward through most of the Tertiary sequence. The groundwater table is located at an elevation of 1300 m within a thrust sheet of Paleozoic carbonates, corresponding to the lower carbonate aquifer hydrostratigraphic unit (LCA3). The LCA3 is considered to be hydraulically connected to the Death Valley regional flow system. The objective of this project is to simulate complex downward patterns of fluid flow and radionuclide transport from the T-tunnel complex through the matrix and fault networks of the Tertiary tuff units to the water table. We developed an improved fracture characterization and mapping methodology consisting of displacement-length scaling relationships, simulation of realistic fault networks based on site-specific data, and the development of novel fracture network upscaling techniques that preserves fracture network flow and transport properties on coarse continuum grid. Development of upscaling method for fracture continua is based on the concepts of discrete fracture network modeling approach which performs better at honoring network connectivity and anisotropy of sparse networks in comparison to other established methods such as a tensor approach. Extensive flow simulations in the dual-continuum framework demonstrate that the characteristics of fault networks strongly influences the saturation profile and formation of perched zones, although they may not conduct a large amount of flow when compared to the matrix continua. The simulated results are found to be very sensitive to distribution of fracture aperture, density of the network, and spatial pattern of fracture clustering. The faults provide rapid pathways for radionuclide transport and the conceptual modeling of diffusional mass transfer between matrix and fracture continua plays a vital role in prediction of the overall behavior of the breakthrough curve.

Geology of the Humboldt region and the Iron King mine, Bigbug mining district, Yavapai County, Arizona

USGS Publications Warehouse

Creasey, Saville Cyrus

1951-01-01

The Humboldt region is in central Yavapai County, Arizona. The intersection of the 112? 15' meridian and the 34? 30' N parallel is in the approximate geographical center of the region, and the Iron King mine is about 2000 feet west-northwest of the intersection. Pre-Cambrian rocks form the bedrock in the Humboldt region. Late Cenozoic unconsolidated river wash and valley fill, including some interbedded basalt, locally mantle the pre-Cambrian rocks, especially in the north-central part of the region (Lonesome Valley). The pre-Cambrian rocks consist of five newly defined metavolcanic formations derived from flows and tuff s, and of six intrusive units ranging in composition from granite to gabbro or perhaps more mafic types. Relic bedding-and pillow structures are locally prominent in the metavolcanics; geopetal structures are uncommon, but where present, generally indicate that the top is toward the west, though the evidence is too meager to be conclusive. Low-grade dynamothermal metamorphism altered the metavolcanics and to a lesser extent the intrusive rocks, forming textures, structures, and mineral assemblages characteristic of low temperature and moderate stress. The Texas Gulch formation, which is the easternmost metavolcanic formation, consists of five lithologic units. Arranged in the general order of their appearance from east to west they are meta-andesite breccia, purple slate, metarhyolite tuff, meta-andesite, and green slate. The boundary between the Texas Gulch formation and the Iron King meta-andesite is apparently gradational. The Iron King meta-andesite consists of three meta-andesite tuff units, two meta-andesite flow units and one metarhyolite tuff and conglomerate unit. The assemblage chlorite-albite-epitode with or without quartz is dominant in the meta-andesites. Mafic intrusive rocks, which may be approximately contemporaneous with metamorphism, may explain the presence of actinolitic hornblende in the central part of the formation. Toward the west the Iron King meta-andesite appears to grade into the Spud Mountain metabreccia through a zone containing beds characteristic of either one formation or the other. The Spud Mountain metabreccia consists of interbedded metabreccia and metatuff beds. The metatuffs are largely andesitic in composition, but a few thin beds of metarhyolite tuff occur. The fragments in the metabreccia beds consist chiefly or porphyritic meta-andesites and the matrix is meta-andesite tuff. Pre-Cambrian faults now marked by dikes separate the Chaparral Gulch metavolcanics, which lie west of the Spud Mountain metabreccia, from underlying and overlying formations. The Chaparral Gulch metavolcanics contain metarhyolite tuff, metarhyolite flow, and meta-andesite tuff that locally was contaminated by rhyolitic detritus. The Indian Hills metavolcanics, which are northeast of the Chaparral Gulch metavolcanics, consist of two broad units, one composed of metarhyolites and the other of meta-andesites. Metamorphosed tuffs and flows are believed to be represented in both units and flow breccia in the meta-andesites. Granite and alaskite; granodiorite and quartz diorite; diorite, mafic quartz diorite, gabbro and diabase; metarhyolite (?); and quartz porphyry comprise the pre-Cambrian intrusive units mapped. They include both deep-seated and hypabyssal types. Dynamothermal metamorphism has foliated the smaller bodies and the margins of the larger masses and partly converted them into mineral assemblages stable under low-grade metamorphic conditions. Planar structures (chiefly foliation) are omnipresent and linear structures are common in the pre-Cambrian meta-volcanic rocks. North-trending planar structures dominate in the Indian Hills metavolcanics, and in the Spud Mountain metabreccia, whereas northeast-trending planar structures are dominant in the Texas Gulch formation, Iron King meta-andesite, and Chaparral Gulch metavolcanics. To a lesser extent northeast-trending st

Recurrent eruption and subsidence at the Platoro caldera complex, southeastern San Juan volcanic field, Colorado: New tales from old tuffs

USGS Publications Warehouse

Lipman, P.W.; Dungan, M.A.; Brown, L.L.; Deino, A.

1996-01-01

Reinterpretation of a voluminous regional ash-flow sheet (Masonic Park Tuff) as two separate tuff sheets of similar phenocryst-rich dacite erupted from separate source calderas has important implications for evolution of the multicyclic Platoro caldera complex and for caldera-forming processes generally. Masonic Park Tuff in central parts of the San Juan field, including the type area, was erupted from a concealed source at 28.6 Ma, but widespread tuff previously mapped as Masonic Park Tuff in the southeastern San Juan Mountains is the product of the youngest large-volume eruption of the Platoro caldera complex at 28.4 Ma. This large unit, newly named the "Chiquito Peak Tuff," is the last-erupted tuff of the Treasure Mountain Group, which consists of at least 20 separate ash-flow sheets of dacite to low-silica rhyolite erupted from the Platoro complex during a 1 m.y. interval (29.5-28.4 Ma). Two Treasure Mountain tuff sheets have volumes in excess of 1000 km3 each, and five more have volumes of 50-150 km3. The total volume of ash-flow tuff exceeds 2500 km3, and caldera-related lavas of dominantly andesitic composition make up 250-500 km3 more. A much greater volume of intermediate-composition magma must have solidified in subcaldera magma chambers. Most preserved features of the Platoro complex - including postcollapse asymmetrical trap-door resurgent uplift of the ponded intracaldera tuff and concurrent infilling by andesitic lava flows - postdate eruption of the Chiquito Peak Tuff. The numerous large-volume pre-Chiquito Peak ash-flow tuffs document multiple eruptions accompanied by recurrent subsidence; early-formed caldera walls nearly coincide with margins of the later Chiquito Peak collapse. Repeated syneruptive collapse at the Platoro complex requires cumulative subsidence of at least 10 km. The rapid regeneration of silicic magmas requires the sustained presence of an andesitic subcaldera magma reservoir, or its rapid replenishment, during the 1 m.y. life span of the Platoro complex. Either case implies large-scale stoping and assimilative recycling of the Tertiary section, including intracaldera tuffs.

Breaking Structural Energy Constraints: Hydrothermal Crystallization of High-Silica Germanosilicates via Building Units Self-Growing Approach.

PubMed

Peng, Mingming; Jiang, Jingang; Liu, Xue; Ma, Yue; Jiao, Meichen; Xu, Hao; Wu, Haihong; He, Mingyuan; Wu, Peng

2018-06-11

Zeolites, a class of crystalline microporous materials, have a wide range of practical applications, in particular serving as key catalysts in petrochemical and finechemical processes. Millions of zeolite topologies are theoretically possible. However, to date, only 235 frameworks with various tetrahedral element compositions have been discovered in nature or artificially synthesized, among which approximately 50 topologies are available in pure silica forms. Germanosilicates are becoming an important zeolite family, with a rapidly increasing number of topological structures with unusual double four-membered-ring (D4R) building units and large-pore or extra large-pore systems. The synthesis of their high-silica analogues with higher (hydro)thermal stability remains a great challenge because the formation of siliceous D4R units is kinetically and thermodynamically unfavorable in hydrothermal systems. Herein, we demonstrate that such D4R-containing high-silica zeolites with unexpected crystalline topologies (ECNU-24-RC and IM-20-RC) are readily constructed through a versatile route. This strategy provides new opportunities for the synthesis of high-silica zeolite catalysts that are hardly obtained by conventional hydrothermal synthesis and it would also facilitate a break-through in increasing the number and types of zeolite materials with practical applications. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Early postcaldera rhyolite and structural resurgence at Long Valley Caldera, California

NASA Astrophysics Data System (ADS)

Hildreth, Wes; Fierstein, Judy; Calvert, Andrew

2017-04-01

After the 767-ka caldera-forming eruption of 650 km3 of rhyolite magma as the Bishop Tuff, 90-100 km3 of similar rhyolite erupted in the west-central part of Long Valley caldera in as many as 40 batches spread over the 110,000-year interval from 750 ka to 640 ka. Centrally, this Early Rhyolite (ER) is as thick as 622 m, but it spread radially to cover much of the caldera floor, where half its area is now concealed by post-ER sediments and lavas. At least 75% of the ER is aphyric rhyolite tuff. Drillholes encountered 22 (altered) ER lava flows intercalated in the pyroclastic pile, and another 11 units of (largely fresh) ER lava are exposed on the caldera's resurgent dome and at Lookout Mountain. Exposed units have been distinguished, mapped, studied petrographically and chemically, and radioisotopically dated; each is described in detail. Their phenocryst contents range from 0 to 2.5 wt%. All the phyric units have plagioclase, orthopyroxene, and ilmenite; most have biotite and rare tiny magnetite, and a few contain rare zircon. The compositional range of fresh obsidians is narrow-74.3-75.0% SiO2, 1.21-1.37% FeO*, and 5.12-5.26% K2O, but wider variations in Ti, Ba, Sr, and Zr permit distinction of individual units and eruptive groups. The limited chemical and petrographic variability shown by so many ER batches released episodically for 110,000 years suggests a thermally buffered and well-stirred reservoir. The ER central area, where ER eruptions had taken place, was uplifted 400 m to form a structural dome 10 km in diameter. Most of the inflation is attributable to 10 sills of ER that intrude the Bishop Tuff beneath the uplift, but other processes potentially contributing to resurgence are also considered. As shown by erratics of Mesozoic rocks ice-rafted from the Sierra Nevada and dropped on ER lavas, much of the ER had erupted early enough and at low enough elevation to be inundated by the intracaldera lake and was only later lifted by the resurgence that also raised clusters of the erratics hundreds of meters higher than any shoreline. Most of the uplift was over by 570 ka, but dome-crossing faults that exhibit normal throw of 10-30 m cut lavas as young as 175-125 ka. For most elements, chemical ranges of the ER lie within those of the zoned Bishop Tuff, which had erupted earlier from the same place. Only Ba, Zr, Hf, and Eu/Eu* extend to ranges outside those of the Bishop Tuff, nominally to less evolved compositions. Initial 87Sr/86Sr values of ER are likewise within the range of the Bishop Tuff, but ER ratios of 143Nd/144Nd and 206Pb/204Pb extend beyond those of the Bishop Tuff to values slightly more influenced by upper-crustal contributions. FeTi-oxide geothermometry yields 752°-844 °C for ER, compared to 700°-820 °C for the Bishop Tuff. ER fO2 values are 0.5-1.0 log units more reduced than those of the T-fO2 array of the Bishop Tuff. The postcaldera reduction may reflect reaction with graphite from the black lithics of Paleozoic graphitic metapelite so abundant in the Bishop Tuff. Much of the pumice emplaced during the later half of the Bishop Tuff eruption has 10-25 wt% phenocrysts, dominantly quartz and sanidine, but the 100 km3 of ER has only 0-2.5 wt% and completely lacks quartz and sanidine. Postcaldera processes, including mixing, volatile ascent, and crystal resorption, as well as potential contaminants and magmatic inputs, are all considered.

Hydraulic conductivity of compacted zeolites.

PubMed

Oren, A Hakan; Ozdamar, Tuğçe

2013-06-01

Hydraulic conductivities of compacted zeolites were investigated as a function of compaction water content and zeolite particle size. Initially, the compaction characteristics of zeolites were determined. The compaction test results showed that maximum dry unit weight (γ(dmax)) of fine zeolite was greater than that of granular zeolites. The γ(dmax) of compacted zeolites was between 1.01 and 1.17 Mg m(-3) and optimum water content (w(opt)) was between 38% and 53%. Regardless of zeolite particle size, compacted zeolites had low γ(dmax) and high w(opt) when compared with compacted natural soils. Then, hydraulic conductivity tests were run on compacted zeolites. The hydraulic conductivity values were within the range of 2.0 × 10(-3) cm s(-1) to 1.1 × 10(-7) cm s(-1). Hydraulic conductivity of all compacted zeolites decreased almost 50 times as the water content increased. It is noteworthy that hydraulic conductivity of compacted zeolite was strongly dependent on the zeolite particle size. The hydraulic conductivity decreased almost three orders of magnitude up to 39% fine content; then, it remained almost unchanged beyond 39%. Only one report was found in the literature on the hydraulic conductivity of compacted zeolite, which is in agreement with the findings of this study.

Subglacial hydrothermal alteration minerals in Jökulhlaup deposits of Southern Iceland, with implications for detecting past or present habitable environments on Mars.

PubMed

Warner, Nicholas H; Farmer, Jack D

2010-06-01

Jökulhlaups are terrestrial catastrophic outfloods, often triggered by subglacial volcanic eruptions. Similar volcano-ice interactions were likely important on Mars where magma/lava may have interacted with the planet's cryosphere to produce catastrophic floods. As a potential analogue to sediments deposited during martian floods, the Holocene sandurs of Iceland are dominated by basaltic clasts derived from the subglacial environment and deposited during jökulhlaups. Palagonite tuffs and breccias, present within the deposits, represent the primary alteration lithology. The surface abundance of palagonite on the sandurs is 1-20%. X-ray diffraction (XRD) analysis of palagonite breccias confirms a mineral assemblage of zeolites, smectites, low-quartz, and kaolinite. Oriented powder X-ray diffractograms (< 2 microm fraction) for palagonite breccia clasts and coatings reveal randomly ordered smectite, mixed layer smectite/illite, zeolites, and quartz. Visible light-near infrared (VNIR) and shortwave infrared (SWIR) lab spectroscopic data of the same palagonite samples show H2O/OH(-) absorptions associated with clays and zeolites. SWIR spectra derived from Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) images of the sandurs reveal Al-OH(-) and Si-OH(-) absorption features. The identified alteration mineral assemblage is consistent with low temperature (100-140 degrees C) hydrothermal alteration of basaltic material within the subglacial environment. These results suggest that potential martian analog sites that contain a similar suite of hydrated minerals may be indicative of past hydrothermal activity and locations where past habitable environments for microbial life may be found.

Common Ion Effects In Zeoponic Substrates: Dissolution And Cation Exchange Variations Due to Additions of Calcite, Dolomite and Wollastonite

NASA Technical Reports Server (NTRS)

Beiersdorfer, R. E.; Ming, D. W.; Galindo, C., Jr.

2003-01-01

c1inoptilolite-rich tuff-hydroxyapatite mixture (zeoponic substrate) has the potential to serve as a synthetic soil-additive for plant growth. Essential plant macro-nutrients such as calcium, phosphorous, magnesium, ammonium and potassium are released into solution via dissolution of the hydroxyapatite and cation exchange on zeolite charged sites. Plant growth experiments resulting in low yield for wheat have been attributed to a Ca deficiency caused by a high degree of cation exchange by the zeolite. Batch-equilibration experiments were performed in order to determine if the Ca deficiency can be remedied by the addition of a second Ca-bearing, soluble, mineral such as calcite, dolomite or wollastonite. Variations in the amount of calcite, dolomite or wollastonite resulted in systematic changes in the concentrations of Ca and P. The addition of calcite, dolomite or wollastonite to the zeoponic substrate resulted in an exponential decrease in the phosphorous concentration in solution. The exponential rate of decay was greatest for calcite (5.60 wt. % -I), intermediate for wollastonite (2.85 wt.% -I) and least for dolomite (1.58 wt.% -I). Additions of the three minerals resulted in linear increases in the calcium concentration in solution. The rate of increase was greatest for calcite (3.64), intermediate for wollastonite (2.41) and least for dolomite (0.61). The observed changes in P and Ca concentration are consistent with the solubilities of calcite, dolomite and wollastonite and with changes expected from a common ion effect with Ca. Keywords: zeolite, zeoponics, common-ion effect, clinoptilolite, hydroxyapatite

Silicate melt inclusion evidence for extreme pre-eruptive enrichment and post-eruptive depletion of lithium in silicic volcanic rocks of the western United States: implications for the origin of lithium-rich brines

USGS Publications Warehouse

Hofstra, Albert H.; Todorov, T.I.; Mercer, C.N.; Adams, D.T.; Marsh, E.E.

2013-01-01

To evaluate whether anatectic and/or highly fractionated lithophile element-enriched rhyolite tuffs deposited in arid lacustrine basins lose enough lithium during eruption, lithification, and weathering to generate significant Li brine resources, pre-eruptive melt compositions, preserved in inclusions, and the magnitude of post-eruptive Li depletions, evident in host rhyolites, were documented at six sites in the western United States. Each rhyolite is a member of the bimodal basalt-rhyolite assemblage associated with extensional tectonics that produced the Basin and Range province and Rio Grande rift, an evolving pattern of closed drainage basins, and geothermal energy or mineral resources. Results from the 0.8 Ma Bishop tuff (geothermal) in California, 1.3 to 1.6 Ma Cerro Toledo and Upper Bandelier tephra (geothermal) and 27.9 Ma Taylor Creek rhyolite (Sn) in New Mexico, 21.7 Ma Spor Mountain tuff (Be, U, F) and 24.6 Ma Pine Grove tuff (Mo) in Utah, and 27.6 Ma Hideaway Park tuff (Mo) in Colorado support the following conclusions. Melt inclusions in quartz phenocrysts from rhyolite tuffs associated with hydrothermal deposits of Sn, Mo, and Be are extremely enriched in Li (1,000s of ppm); those from Spor Mountain have the highest Li abundance yet recorded (max 5,200 ppm, median 3,750 ppm). Forty-five to 98% of the Li present in pre-eruptive magma was lost to the environment from these rhyolite tuffs. The amount of Li lost from the small volumes (1–10 km3) of Li-enriched rhyolite deposited in closed basins is sufficient to produce world-class Li brine resources. After each eruption, meteoric water leaches Li from tuff, which drains into playas, where it is concentrated by evaporation. The localized occurrence of Li-enriched rhyolites may explain why brines in arid lacustrine basins seldom have economic concentrations of Li. Considering that hydrothermal deposits of Sn, Mo, Be, U, and F may indicate potential for Li brines in nearby basins, we surmise that the world’s largest Li brine resource in the Salar de Uyuni (10 Mt) received Li from nearby rhyolite tuffs in the Bolivian tin belt.

On the physics of unstable infiltration, seepage, and gravity drainage in partially saturated tuffs

DOE Office of Scientific and Technical Information (OSTI.GOV)

Faybishenko, B.; Bodvarsson, G.S.; Salve, R.

2002-04-01

To improve understanding of the physics of dynamic instabilities in unsaturated flow processes within the Paintbrush nonwelded unit (PTn) and the middle nonlithophysal portion of the Tonopah Spring welded tuff unit (TSw) of Yucca Mountain, we analyzed data from a series of infiltration tests carried out at two sites (Alcove 4 and Alcove 6) in the Exploratory Studies Facility, using analytical and empirical functions. The analysis of infiltration rates measured at both sites showed three temporal scales of infiltration rate: (1) a macro-scale trend of overall decreasing flow, (2) a meso-scale trend of fast and slow motion exhibiting three-stage variationsmore » of the flow rate (decreasing, increasing, and [again] decreasing flow rate, as observed in soils in the presence of entrapped air), and (3) micro-scale (high frequency) fluctuations. Infiltration tests in the nonwelded unit at Alcove 4 indicate that this unit may effectively dampen episodic fast infiltration events; however, well-known Kostyakov, Horton, and Philip equations do not satisfactorily describe the observed trends of the infiltration rate. Instead, a Weibull distribution model can most accurately describe experimentally determined time trends of the infiltration rate. Infiltration tests in highly permeable, fractured, welded tuff at Alcove 6 indicate that the infiltration rate exhibits pulsation, which may have been caused by multiple threshold effects and water-air redistribution between fractures and matrix. The empirical relationships between the extrinsic seepage from fractures, matrix imbibition, and gravity drainage versus the infiltration rate, as well as scaling and self-similarity for the leading edge of the water front are the hallmark of the nonlinear dynamic processes in water flow under episodic infiltration through fractured tuff. Based on the analysis of experimental data, we propose a conceptual model of a dynamic fracture flow and fracture-matrix interaction in fractured tuff, incorporating the time dependent processes of water redistribution in the fracture-matrix system.« less

Geochemistry and Geochronology of Middle Tertiary Volcanic Rocks of the Central Chiricahua Mountains, Southeast Arizona

USGS Publications Warehouse

du Bray, Edward A.; Pallister, John S.; Snee, Lawrence W.

2004-01-01

Middle Tertiary volcanic rocks of the central Chiricahua Mountains in southeast Arizona are the westernmost constituents of the Eocene-Oligocene Boot Heel volcanic field of southwestern New Mexico and southeastern Arizona. About two dozen volumetric ally and stratigraphically significant volcanic units are present in this area. These include large-volume, regionally distributed ash-flow tuffs and smaller volume, locally distributed lava flows. The most voluminous of these units is the Rhyolite Canyon Tuff, which erupted 26.9 million years ago from the Turkey Creek caldera in the central Chiricahua Mountains. The Rhyolite Canyon Tuff consists of 500-1,000 cubic kilometers of rhyolite that was erupted from a normally zoned reservoir. The tuff represents sequential eruptions, which became systematically less geochemically evolved with time, from progressively deeper levels of the source reservoir. Like the Rhyolite Canyon Tuff, other ashflow tuffs preserved in the central Chiricahua Mountains have equivalents in nearby, though isolated mountain ranges. However, correlation of these other tuffs, from range to range, has been hindered by stratigraphic discontinuity, structural complexity, and various lithologic similarities and ambiguities. New geochemical and geochronologic data presented here enable correlation of these units between their occurrences in the central Chiricahua Mountains and the remainder of the Boot Heel volcanic field. Volcanic rocks in the central Chiricahua Mountains are composed dominantly of weakly peraluminous, high-silica rhyolite welded tuff and rhyolite lavas of the high-potassium and shoshonitic series. Trace-element, and to a lesser extent, major-oxide abundances are distinct for most of the units studied. Geochemical and geochronologic data depict a time and spatial transgression from subduction to within-plate and extensional tectonic settings. Compositions of the lavas tend to be relatively homogeneous within particular units. In contrast, compositions of the ash-flow tuffs, including the Rhyolite Canyon Tuff, vary significantly owing to eruption from compositionally zoned reservoirs. Reservoir zonation is consistent with fractional crystallization of observed phenocryst phases and resulting residual liquid compositional evolution. Rhyolite lavas preserved in the moat of the Turkey Creek caldera depict compositional zonation that is the reverse of that expected of magma extraction from progressively deeper parts of a normally zoned reservoir. Presuming that the source reservoir was sequentially tapped from its top downward, development of reverse zonation in the rhyolite lava sequence may indicate that later erupted, more evolved magma contains systematically less wallrock contamination derived from the geochemically primitive margins of its incompletely mixed reservoir. New 40Ar/39Ar geochronology data indicate that the principal middle Tertiary volcanic rocks in the central Chiricahua Mountains were erupted between about 34.2 and 26.2 Ma, and that the 5.2 m.y. period between 33.3 and 28.1 Ma was amagmatic. The initial phase of eruptive activity in the central Chiricahua Mountains, between 34.2 and 33.3 Ma, was associated with a regional tectonic regime dominated by subduction along the west edge of North America. We infer that the magmatic hiatus, nearly simultaneous with a hiatus of similar duration in parts of the Boot Heel volcanic field east of the central Chiricahua Mountains, is related to a period of more rapid convergence and therefore shallower subduction that may have displaced subduction-related magmatic activity to a position east of the present-day Boot Heel volcanic field. The hiatus also coincides with a major plate tectonic reorganization along the west edge of North America that resulted in cessation of subduction and initiation of transform faulting along the San Andreas fault. The final period of magmatism in the central Chiricahua Mountains, between 28.1 and 23.2 Ma, ap

3D Model of the McGinness Hills Geothermal Area

DOE Data Explorer

Faulds, James E.

2013-12-31

The McGinness Hills geothermal system lies in a ~8.5 km wide, north-northeast trending accommodation zone defined by east-dipping normal faults bounding the Toiyabe Range to the west and west-dipping normal faults bounding the Simpson Park Mountains to the east. Within this broad accommodation zone lies a fault step-over defined by north-northeast striking, west-dipping normal faults which step to the left at roughly the latitude of the McGinness Hills geothermal system. The McGinness Hills 3D model consists of 9 geologic units and 41 faults. The basal geologic units are metasediments of the Ordovician Valmy and Vininni Formations (undifferentiated in the model) which are intruded by Jurassic granitic rocks. Unconformably overlying is a ~100s m-thick section of Tertiary andesitic lava flows and four Oligocene-to-Miocene ash-flow tuffs: The Rattlesnake Canyon Tuff, tuff of Sutcliffe, the Cambell Creek Tuff and the Nine Hill tuff. Overlying are sequences of pre-to-syn-extensional Quaternary alluvium and post-extensional Quaternary alluvium. 10-15º eastward dip of the Tertiary stratigraphy is controlled by the predominant west-dipping fault set. Geothermal production comes from two west dipping normal faults in the northern limb of the step over. Injection is into west dipping faults in the southern limb of the step over. Production and injection sites are in hydrologic communication, but at a deep level, as the northwest striking fault that links the southern and northern limbs of the step-over has no permeability.

One-step synthesis of mesoporous pentasil zeolite with single-unit-cell lamellar structural features

DOEpatents

Tsapstsis, Michael; Zhang, Xueyi

2015-11-17

A method for making a pentasil zeolite material includes forming an aqueous solution that includes a structure directing agent and a silica precursor; and heating the solution at a sufficient temperature and for sufficient time to form a pentasil zeolite material from the silica precursor, wherein the structure directing agent includes a quaternary phosphonium ion.

Absolute Paleointensity Study of Miocene Tiva Canyon Tuff, Yucca Mountain, Nevada

NASA Astrophysics Data System (ADS)

Patiman, A.; Bowles, J.

2014-12-01

Unoriented samples from the ~12.7 Ma Tiva Canyon (TC) tuff from Yucca Mountain, Nevada are studied in terms of magnetic properties and geomagnetic paleointensity. The magnetic mineralogy and magnetic properties of the TC tuff have previously been well documented, and the remanence-carrier in ~15-m thick zones at the top and bottom of the unit is dominantly is single domain (SD) to superparamagnetic (SP) magnetite, which may be considered ideal for absolute paleointensity studies. Among one of the several episodic volcanic eruptions of the Southwestern Nevada Volcanic Field (SWNVF), the welded TC tuff belongs to the Paintbrush Group. Here we present magnetic properties from two previously unreported sections of the TC tuff, as well as Thellier-type absolute paleointensity estimates. Samples were collected from the lower ~7 m at the base of the flow. Magnetic properties studied include hysteresis, bulk magnetic susceptibility, frequency-dependent susceptibility, and anhysteretic remanent magnetization acquisition. Magnetic property results are consistent with earlier work, showing that the main magnetic mineral is magnetite. SP samples are dominant from the lower ~1 m to ~3.6 m basal unit while the middle unit of ~3.7 m to 7.0 m mainly consists of SD samples. The paleointensity results are closely tied to the stratigraphic height and magnetic properties linked to domain state. The SD samples have consistent absolute paleointensity values 32.40±0.22 uT, VADM 5.74*1022 A.m2 and behaved ideally during paleointensity experiments. The SP samples have consistently higher paleointensity and less ideal behavior, but would likely pass many traditional quality-control tests. Since the magnetite has been interpreted to form by precipitation out of the glass post-emplacement, but at temperatures higher than the Curie temperature, we tentatively interpret the SD remanence to be a primary thermal remanent magnetization and the paleointensity result to be a valid estimate of geomagnetic paleointensity for the Miocene. Post-emplacement vapor-phase alteration might be expected to alter magnetic mineralogy and magnetization, and has been reported in the upper portions of the TC tuff, but not in the lower sections discussed here.

Geohydrology of Monitoring Wells Drilled in Oasis Valley near Beatty, Nye County, Nevada, 1997

USGS Publications Warehouse

Robledo, Armando R.; Ryder, Philip L.; Fenelon, Joseph M.; Paillet, Frederick L.

1999-01-01

Twelve monitoring wells were installed in 1997 at seven sites in and near Oasis Valley, Nevada. The wells, ranging in depth from 65 to 642 feet, were installed to measure water levels and to collect water-quality samples. Well-construction data and geologic and geophysical logs are presented in this report. Seven geologic units were identified and described from samples collected during the drilling: (1) Ammonia Tanks Tuff; (2) Tuff of Cutoff Road; (3) tuffs, not formally named but informally referred to in this report as the 'tuff of Oasis Valley'; (4) lavas informally named the 'rhyolitic lavas of Colson Pond'; (5) Tertiary colluvial and alluvial gravelly deposits; (6) Tertiary and Quaternary colluvium; and (7) Quaternary alluvium. Water levels in the wells were measured in October 1997 and February 1998 and ranged from about 18 to 350 feet below land surface. Transmissive zones in one of the boreholes penetrating volcanic rock were identified using flowmeter data. Zones with the highest transmissivity are at depths of about 205 feet in the 'rhyolitic lavas of Colson Pond' and 340 feet within the 'tuff of Oasis Valley.'

Preliminary report on the geology and geophysics of drill hole UE25a-1, Yucca Mountain, Nevada Test Site

USGS Publications Warehouse

Spengler, Richard W.; Muller, D.C.; Livermore, R.B.

1979-01-01

A subsurface geologic study in connection with the Nevada Nuclear Waste Storage Investigations has furnished detailed stratigraphic and structural information about tuffs underlying northeastern Yucca Mountain on the Nevada Test Site. Drill hole UE25a-1 penetrated thick sequences of nonwelded to densely welded ash-flow and bedded tuffs of Tertiary age. Stratigraphic units that were identified from the drill-hole data include the Tiva Canyon and Topopah Spring Members of the Paintbrush Tuff, tuffaceous beds of Calico Hills, and the Prow Pass and Bullfrog Members of the Crater Flat Tuff. Structural analysis of the core indicated densely welded zones to be highly fractured. Many fractures show near-vertical inclinations and are commonly coated with secondary silica, manganese and iron oxides, and calcite. Five fault zones were recognized, most of which occurred in the Topopah Spring Member. Shear fractures commonly show oblique-slip movement and some suggest a sizable component of lateral compression. Graphic logs are included that show the correlation of lithology, structural properties, and geophysical logs. Many rock units have characteristic log responses but highly fractured zones, occurring principally in the Tiva Canyon and Topopah Spring Members, restricted log coverage to the lower half of the drill hole.

Hydrology of the unsaturated zone, Yucca Mountain, Nevada

USGS Publications Warehouse

Lecain, Gary D.; Stuckless, John S.

2012-01-01

The unsaturated zone at Yucca Mountain was investigated as a possible site for the nation's first high-level nuclear waste repository. Scientific investigations included infiltration studies, matrix properties testing, borehole testing and monitoring, underground excavation and testing, and the development of conceptual and numerical models of the hydrologic processes at Yucca Mountain. Infiltration estimates by empirical and geochemical methods range from 0.2 to 1.4 mm/yr and 0.2–6.0 mm/yr, respectively. Infiltration estimates from numerical models range from 4.5 mm/yr to 17.6 mm/yr. Rock matrix properties vary vertically and laterally as the result of depositional processes and subsequent postdepositional alteration. Laboratory tests indicate that the average matrix porosity and hydraulic conductivity values for the main level of the proposed repository (Topopah Spring Tuff middle nonlithophysal zone) are 0.08 and 4.7 × 10−12 m/s, respectively. In situ fracture hydraulic conductivity values are 3–6 orders of magnitude greater. The permeability of fault zones is approximately an order of magnitude greater than that of the surrounding rock unit. Water samples from the fault zones have tritium concentrations that indicate some component of postnuclear testing. Gas and water vapor movement through the unsaturated zone is driven by changes in barometric pressure, temperature-induced density differences, and wind effects. The subsurface pressure response to surface barometric changes is controlled by the distribution and interconnectedness of fractures, the presence of faults and their ability to conduct gas and vapor, and the moisture content and matrix permeability of the rock units. In situ water potential values are generally less than −0.2 MPa (−2 bar), and the water potential gradients in the Topopah Spring Tuff units are very small. Perched-water zones at Yucca Mountain are associated with the basal vitrophyre of the Topopah Spring Tuff or the Calico Hills bedded tuff. Thermal gradients in the unsaturated zone vary with location, and range from ~2.0 °C to 6.0 °C per 100 m; the variability appears to be associated with topography. Large-scale heater testing identified a heat-pipe signature at ~97 °C, and identified thermally induced and excavation-induced changes in the stress field. Elevated gas-phase CO2 concentrations and a decrease in the pH of water from the condensation zone also were identified. Conceptual and numerical flow and transport models of Yucca Mountain indicate that infiltration is highly variable, both spatially and temporally. Flow in the unsaturated zone is predominately through fractures in the welded units of the Tiva Canyon and Topopah Spring Tuffs and predominately through the matrix in the Paintbrush Tuff nonwelded units and Calico Hills Formation. Isolated, transient, fast-flow paths, such as faults, do exist but probably carry only a small portion of the total liquid-water flux at Yucca Mountain. The Paintbrush Tuff nonwelded units act as a storage buffer for transient infiltration pulses. Faults may act as flow boundaries and/or fast pathways. Below the proposed repository horizon, low-permeability lithostratigraphic units of the Topopah Spring Tuff and/or the Calico Hills Formation may divert flow laterally to faults that act as conduits to the water table. Advective transport pathways are consistent with flow pathways. Matrix diffusion is the major mechanism for mass transfer between fractures and the matrix and may contribute to retardation of radionuclide transport when fracture flow is dominant. Sorption may retard the movement of radionuclides in the unsaturated zone; however, sorption on mobile colloids may enhance radionuclide transport. Dispersion is not expected to be a major transport mechanism in the unsaturated zone at Yucca Mountain. Natural analogue studies support the concepts that percolating water may be diverted around underground openings and that the percentage of infiltration that becomes seepage decreases as infiltration decreases.

Geology of the Yucca Mountain region

USGS Publications Warehouse

Stuckless, J.S.; O'Leary, Dennis W.

2006-01-01

Yucca Mountain has been proposed as the site for the nation's first geologic repository for high-level radioactive waste. This chapter provides the geologic framework for the Yucca Mountain region. The regional geologic units range in age from late Precambrian through Holocene, and these are described briefly. Yucca Mountain is composed dominantly of pyroclastic units that range in age from 11.4 to 15.2 Ma. The proposed repository would be constructed within the Topopah Spring Tuff, which is the lower of two major zoned and welded ash-flow tuffs within the Paintbrush Group. The two welded tuffs are separated by the partly to nonwelded Pah Canyon Tuff and Yucca Mountain Tuff, which together figure prominently in the hydrology of the unsaturated zone. The Quaternary deposits are primarily alluvial sediments with minor basaltic cinder cones and flows. Both have been studied extensively because of their importance in predicting the long-term performance of the proposed repository. Basaltic volcanism began ca. 10 Ma and continued as recently as ca. 80 ka with the eruption of cones and flows at Lathrop Wells, ???10 km south-southwest of Yucca Mountain. Geologic structure in the Yucca Mountain region is complex. During the latest Paleozoic and Mesozoic, strong compressional forces caused tight folding and thrust faulting. The present regional setting is one of extension, and normal faulting has been active from the Miocene through to the present. There are three major local tectonic domains: (1) Basin and Range, (2) Walker Lane, and (3) Inyo-Mono. Each domain has an effect on the stability of Yucca Mountain. ?? 2007 Geological Society of America. All rights reserved.

Geohydrologic data and test results from Well J-13, Nevada Test Site, Nye County, Nevada

DOE Office of Scientific and Technical Information (OSTI.GOV)

Thordarson, W.

Well J-13 was drilled to a depth of 1063.1 meters by using air-hydraulic-rotary drilling equipment. The well penetrated 135.6 meters of alluvium of Quaternary and Tertiary age and 927.5 meters of tuff of Tertiary age. The Topopah Spring Member of the Paintbrush Tuff, the principal aquifer, was penetrated from depths of 207.3 to 449.6 meters; a pumping test indicated its transmissivity is 120 meters squared per day, and its hydraulic conductivity is 1.0 meters per day. Below the Topopah Spring Member, tuff units are confining beds; transmissivities range from 0.10 to 4.5 meters squared per day, and hydraulic conductivities rangemore » from 0.0026 to 0.15 meter per day. Confining beds penetrated below a depth of 719.3 meters had the smallest transmissivities (0.10 to 0.63 meter squared per day) and hydraulic conductivities (0.0026 to 0.0056 meter per day). A static water level of about 282.2 meters was measured for the various water-bearing tuff units above a depth of 645.6 meters. Below a depth of 772.7 meters, the static water level was slightly deeper, 283.3 to 283.6 meters. Ground water sampled from well J-13 is a sodium bicarbonate water containing small concentrations of calcium, magnesium, silica, and sulfate, which is a typical analysis of water from tuff. Apparent age of the ground water, derived from carbon-14 age dating, is 9900 years. 15 references, 24 figures, 13 tables.« less

Nonmarine facies in the Late Triassic(?) to Early Jurassic Horn Mountain Tuff member of the Talkeetna Formation, Horn Mountain, lower Cook Inlet basin, Alaska

USGS Publications Warehouse

LePain, D.L.; Stanley, Richard G.; Helmold, K.P.

2016-01-01

The Talkeetna Formation is a prominent lithostratigraphic unit in south-central Alaska. In the Iniskin–Tuxedni area, Detterman and Hartsock (1966) divided the formation into three mappable units including, from oldest to youngest, the Marsh Creek Breccia, the Portage Creek Agglomerate, and the Horn Mountain Tuff Members. The Horn Mountain Tuff Member was thought to include rocks deposited in a nonmarine setting based on the presence of “tree stumps in an upright position” (Detterman and Hartsock, 1966, p. 19) near the top of the type section at Horn Mountain. Bull (2015) recognized possible nonmarine volcaniclastic rocks in the member during the 2014 field season in a saddle on the north side of Horn Mountain (figs. 2-1 and 2-2). The authors visited this location in 2015 and measured a short stratigraphic section to document facies, interpret depositional setting, and constrain age. This report summarizes our field observations and presents preliminary interpretations.

Environmental effect and genetic influence: a regional cancer predisposition survey in the Zonguldak region of Northwest Turkey

NASA Astrophysics Data System (ADS)

Kadir, Selahattin; Önen-Hall, A. Piril; Aydin, S. Nihal; Yakicier, Cengiz; Akarsu, Nurten; Tuncer, Murat

2008-03-01

The Cretaceous-Eocene volcano-sedimentary units of the Zonguldak region of the western Black Sea consist of subalkaline andesite and tuff, and sandstone dominated by smectite, kaolinite, accessory chlorite, illite, mordenite, and analcime associated with feldspar, quartz, opal-CT, amphibole, and calcite. Kaolinization, chloritization, sericitization, albitization, Fe-Ti-oxidation, and the presence of zeolite, epidote, and illite in andesitic rocks and tuffaceous materials developed as a result of the degradation of a glass shards matrix, enclosed feldspar, and clinopyroxene-type phenocrysts, due to alteration processes. The association of feldspar and glass with smectite and kaolinite, and the suborientation of feldspar-edged, subparallel kaolinite plates to fracture axes may exhibit an authigenic smectite or kaolinite. Increased alteration degree upward in which Al, Fe, and Ti are gained, and Si, Na, K, and Ca are depleted, is due to the alteration following possible diagenesis and hydrothermal activities. Micromorphologically, fibrous mordenite in the altered units and the presence of needle-type chrysotile in the residential buildings in which cancer cases lived were detected. In addition, the segregation pattern of cancer susceptibility in the region strongly suggested an environmental effect and a genetic influence on the increased cancer incidence in the region. The most likely diagnosis was Li-Fraumeni syndrome, which is one of the hereditary cancer predisposition syndromes; however, no mutations were observed in the p53 gene, which is the major cause of Li-Fraumeni syndrome. The micromorphology observed in the altered units in which cancer cases were detected may have a role in the expression of an unidentified gene, but does not explain alone the occurrence of cancer as a primary cause in the region.

Tuff of Bridge Spring: A mid-Miocene ash-flow tuff, northern Colorado River extensional corridor, Nevada and Arizona

DOE Office of Scientific and Technical Information (OSTI.GOV)

Smith, E.I.; Morikawa, S.A.; Martin, M.W.

1993-04-01

The Tuff of Bridge Spring (TBS) (15.19[+-]0.02 Ma; Gans, 1991) is a compositionally variable dacite to rhyolite ash-flow tuff that crops out over 1800 sq. km in the northern Colorado River extensional corridor. The TBS varies in composition from 59.5 to 74 wt. % SiO[sub 2] and typically contains phenocrysts of sanidine, plagioclase, biotite, clinopyroxene, [+-] sphene, [+-] apatite, [+-] zircon, and [+-] hornblende. The TBS is thickest and displays its greatest compositional range in the center of its area of exposure. The McCullough Range section contains at least three chemically distinct flow units that vary in composition from dacitemore » to rhyolite. The basal and uppermost units are normally zoned and the middle unit is reversely zoned. The complex chemical zonation and zoning reversals in the TBS indicate that it erupted from a magma chamber that was periodically injected by both mafic and felsic magmas. Sections at the edge of the exposure area are thin, contain only one or two chemically definable flow units and have a limited compositional range. To the west at Sheep Mountain, TBS is 2.9 m thick and ranges from 70.2--71.7 wt % SiO[sub 2]. To the east in the White Hills, TBS is 14 m thick and ranges from 59.5--65.3 wt % SiO[sub 2]. This chemical and field data indicate that although the TBS is regionally extensive, individual flow units are not. Isotopic data and chemistry suggest that all sections of the TBS are cogenetic. Comparisons of chemical, geochronological and isotopic data between the TBS and nearby coeval plutons indicate that the Aztec Wash (Eldorado Mts., Nevada) and Mt. Perkins (Black Mountain, Arizona) plutons are possible source for the TBS. Both plutons exhibit ample evidence of magma mixing and commingling, processes that may produce compositional zonation such as that observed in the TBS.« less

Antimicrobial efficacy and longevity of silver+zeolite incorporating preinsulated ducts installed in real healthcare settings.

PubMed

Tinteri, C; Potenza, M; Rizzetto, R

2012-12-01

The values of microbial growth in the air exiting from the heating, ventilation and air conditioning (HVAC) ducts treated with silver/zeolite have been shown to be lower than those in the air coming out the traditional metal ones. This study aims to verify how long this antimicrobial activity lasts. All the tests were performed according to US ASTM E2180-01 and ISO-JIZ 22196 standards. Samples of aluminum cladding panels of different thickness and incorporating silver-zeolite were tested in order to verify their thickness depending antibacterial activity. The same kind of linings samples were analyzed after a simulated and accelerated ageing process. Ag-zeolite incorporating HVAC duct panels linings were tested after years from their installation, in order to verify the maintenance of their bactericidal power during time. For laminates containing different amounts of silver+Zeolite it was shown that also in panels with minimum thickness tested, the lowest germicidal effect (GE) found was still very good (GE of 5,76 ULog10). After their wearing and tearing the antimicrobial activity tended to increase passing from 7.2081 to 8.29922 LogUnits in panels 80 microns thick. For still hospital working aluminium foils incorporating Silver/Zeolite on panels installed through 2006 and 2008, the antimicrobial action of zeolite was still firmly present even after two years and three years.The germicidal effect standards were maintained even during time on constant values between 7.477 and 7.086 LogUnits. The persistence of bactericidal efficacy of Ag+zeolite treatment in all the materials used for the construction of HVAC ductworks can be confirmed.

Petrographic and geochemical characteristics of a section through the Tiva Canyon Tuff at Antler Ridge, Yucca Mountain, Nevada

DOE Office of Scientific and Technical Information (OSTI.GOV)

Singer, F.R.; Widmann, B.L.; Dickerson, R.P.

1994-12-31

The Tiva Canyon Tuff of the Paintbrush Group of Miocene age caps much of Yucca Mountain, Nevada and is a compositionally zoned, compound cooling, pyroclastic flow that ranges from a dominantly high-silica rhyolitic base to a quartz-latitic caprock. Petrographic and geochemical studies have focused on rigorously defining the internal stratigraphy of this unit to support the detailed mapping of the Ghost Dance fault and other structures in the central fault block of Yucca Mountain. This study shows that devitrification textures and vapor phase mineralogy, in addition to other physical attributes such as pumice variability (flattening) and crystal content, can bemore » used as distinguishing criteria to better define lithologic zones within the Tiva Canyon Tuff. In addition, the study also shows that the petrographic textures and chemistry of the groundmass vary systematically within recognizable lithologic zones and may be used to characterize and vertically divide litho-stratigraphic zones within the Tiva Canyon Tuff.« less

The influence of adsorbed molecules on the framework vibrations of Na-Faujasites studied with FT Raman spectroscopy

NASA Astrophysics Data System (ADS)

Ferwerda, R.; van der Maas, J. H.

1995-11-01

The use of FT Raman spectroscopy in the elucidation of the structural parameters of Faujasitic zeolites is investigated. Because fluorescence is less of a problem on excitation with a near-infrared laser, FT Raman spectroscopy allows one to probe the effects of in situ heat treatments on the zeolite structure. A correlation is found between the bending vibrations of the Y zeolites and their unit cell size. The vibrations, however, are severely influenced by the charge distribution within the zeolite. Hence, the position of the charge-balancing cations and the water content affect the Raman spectra. Pyridine adsorption results in a rearrangement of the cations or water molecules still present in the structure after activation, and thus alters the vibrations of the zeolite lattice.

Characterization of sonicated natural zeolite/ferric chloride hexahydrate by infrared spectroscopy

NASA Astrophysics Data System (ADS)

Prasetyo, T. A. B.; Soegijono, B.

2018-03-01

The characteristics of sonicated Bayah natural zeolite with and without ferric chloride hexahydrate solution using infrared method has been studied. High intensity ultrasonic waves were exposed to the samples for 40 min, 80 min and 120 min. Infra red spectra analysis was conducted to evaluate zeolite vibrational spectrum contributions, namely, the vibrations from the framework of the zeolite, from the charge-balancing cations, and from the relatively isolated groups, such as the surface OH groups and their behavior after sonication process. An addition of FeCl3.6H2O and sonication process on natural zeolite improved secondary building units link by forming oxygen bridges and also close relationship with duration of applied high intensity ultrasonic process. Longer ultrasonic process resulted in more increment of O-H absorbance.

Metal Oxide/Zeolite Combination Absorbs H2S

NASA Technical Reports Server (NTRS)

Voecks, Gerald E.; Sharma, Pramod K.

1989-01-01

Mixed copper and molybdenum oxides supported in pores of zeolite found to remove H2S from mixture of gases rich in hydrogen and steam, at temperatures from 256 to 538 degree C. Absorber of H2S needed to clean up gas streams from fuel processors that incorporate high-temperature steam reformers or hydrodesulfurizing units. Zeolites chosen as supporting materials because of their high porosity, rigidity, alumina content, and variety of both composition and form.

Construction of Zeolite-Like Cluster Organic Frameworks from 3 d-4 d/3 d-3 d Heterometallic Supertetrahedral Secondary Building Units: Syntheses, Structures, and Properties.

PubMed

Lin, Li-Dan; Deng, Chu-Chu; Zhao, D; Li, Xin-Xiong; Zheng, Shou-Tian

2018-01-02

Two zeolite-like cluster organic frameworks based on Cd-Cu/Mn-Cu heterometallic supertetrahedral secondary building units have been successfully constructed under solvothermal conditions, namely, Cu[Cd 4 Cu 6 (L) 4 (H 2 O) 18 ](Ac) 9 ⋅DMA⋅3 H 2 O (1), and Cu[Mn 4 Cu 6 (L) 4 (Ac) 3 (H 2 O) 12 ](Ac) 6 ⋅CH 3 CN⋅13 H 2 O (2), where H 3 L=2-(hydroxymethyl)-2-(pyridin-4-yl)-1,3-propanediol, Ac=CH 3 COO - , DMA=N,N'-dimethylacetamide. Single-crystal X-ray structural analysis reveals that both 1 and 2 exhibit 3-dimensional zeolite-like architectures with similar 4-connected components, but possess definitely different topologies of diamondoid (dia) and uncommon lonsdaleite (lon), respectively. 1 and 2 represent the first cases of zeolite-like cluster organic frameworks containing Cd-Cu/Mn-Cu heterometallic supertetrahedral secondary building units. Furthermore, the magnetic properties and porous nature of 1 and 2 were also studied. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Quantification of thickness and wrinkling of exfoliated two-dimensional zeolite nanosheets

DOE Office of Scientific and Technical Information (OSTI.GOV)

Kumar, Prashant; Agrawal, Kumar Varoon; Tsapatsis, Michael

Some two-dimensional (2D) exfoliated zeolites are single- or near single-unit cell thick silicates that can function as molecular sieves. Although they have already found uses as catalysts, adsorbents and membranes precise determination of their thickness and wrinkling is critical as these properties influence their functionality. Here we demonstrate a method to accurately determine the thickness and wrinkles of a 2D zeolite nanosheet by comprehensive 3D mapping of its reciprocal lattice. Since the intensity modulation of a diffraction spot on tilting is a fingerprint of the thickness, and changes in the spot shape are a measure of wrinkling, this mapping ismore » achieved using a large-angle tilt-series of electron diffraction patterns. As a result, application of the method to a 2D zeolite with MFI structure reveals that the exfoliated MFI nanosheet is 1.5 unit cells (3.0 nm) thick and wrinkled anisotropically with up to 0.8 nm average surface roughness.« less

Quantification of thickness and wrinkling of exfoliated two-dimensional zeolite nanosheets

DOE PAGES

Kumar, Prashant; Agrawal, Kumar Varoon; Tsapatsis, Michael; ...

2015-05-11

Some two-dimensional (2D) exfoliated zeolites are single- or near single-unit cell thick silicates that can function as molecular sieves. Although they have already found uses as catalysts, adsorbents and membranes precise determination of their thickness and wrinkling is critical as these properties influence their functionality. Here we demonstrate a method to accurately determine the thickness and wrinkles of a 2D zeolite nanosheet by comprehensive 3D mapping of its reciprocal lattice. Since the intensity modulation of a diffraction spot on tilting is a fingerprint of the thickness, and changes in the spot shape are a measure of wrinkling, this mapping ismore » achieved using a large-angle tilt-series of electron diffraction patterns. As a result, application of the method to a 2D zeolite with MFI structure reveals that the exfoliated MFI nanosheet is 1.5 unit cells (3.0 nm) thick and wrinkled anisotropically with up to 0.8 nm average surface roughness.« less

Evidence for large-magnitude, post-Eocene extension in the northern Shoshone Range, Nevada, and its implications for Carlin-type gold deposits in the lower plate of the Roberts Mountains allochthon

USGS Publications Warehouse

Colgan, Joseph P.; Henry, Christopher D.; John, David A.

2014-01-01

The northern Shoshone and Toiyabe Ranges in north-central Nevada expose numerous areas of mineralized Paleozoic rock, including major Carlin-type gold deposits at Pipeline and Cortez. Paleozoic rocks in these areas were previously interpreted to have undergone negligible postmineralization extension and tilting, but here we present new data that suggest major post-Eocene extension along west-dipping normal faults. Tertiary rocks in the northern Shoshone Range crop out in two W-NW–trending belts that locally overlie and intrude highly deformed Lower Paleozoic rocks of the Roberts Mountains allochthon. Tertiary exposures in the more extensive, northern belt were interpreted as subvertical breccia pipes (intrusions), but new field data indicate that these “pipes” consist of a 35.8 Ma densely welded dacitic ash flow tuff (informally named the tuff of Mount Lewis) interbedded with sandstones and coarse volcaniclastic deposits. Both tuff and sedimentary rocks strike N-S and dip 30° to 70° E; the steeply dipping compaction foliation in the tuffs was interpreted as subvertical flow foliation in breccia pipes. The southern belt along Mill Creek, previously mapped as undivided welded tuff, includes the tuff of Cove mine (34.4 Ma) and unit B of the Bates Mountain Tuff (30.6 Ma). These tuffs dip 30° to 50° east, suggesting that their west-dipping contacts with underlying Paleozoic rocks (previously mapped as depositional) are normal faults. Tertiary rocks in both belts were deposited on Paleozoic basement and none appear to be breccia pipes. We infer that their present east tilt is due to extension on west-dipping normal faults. Some of these faults may be the northern strands of middle Miocene (ca. 16 Ma) faults that cut and tilted the 34.0 Ma Caetano caldera ~40° east in the central Shoshone Range (

Geological nature of mineral licks and the reasons for geophagy among animals

NASA Astrophysics Data System (ADS)

Panichev, Alexander M.; Popov, Vladimir K.; Chekryzhov, Igor Yu.; Seryodkin, Ivan V.; Sergievich, Alexander A.; Golokhvast, Kirill S.

2017-06-01

In this paper, the reasons for geophagy (the eating of rocks by wild herbivores) in two regions of the eastern Sikhote-Alin volcanic belt are considered. The mineralogical and chemical features of the consumed rocks, as well as the geological conditions of their formation, are investigated. A comparative analysis of the mineral and chemical composition of the consumed rocks and the excrement of the animals, almost completely consisting of mineral substances, is carried out. It is established that the consumed rocks are hydrothermally altered rhyolitic tuffs located in the volcanic calderas and early Cenozoic volcano-tectonic depressions. They consist of 30-65 % from zeolites (mainly clinoptilolites) and smectites, possessing powerful sorption properties. According to the obtained data, the main reason for geophagy may be connected with the animals' urge to discard excessive and toxic concentrations of certain elements that are widespread in specific habitats and ingested with forage plants.

A database of new zeolite-like materials.

PubMed

Pophale, Ramdas; Cheeseman, Phillip A; Deem, Michael W

2011-07-21

We here describe a database of computationally predicted zeolite-like materials. These crystals were discovered by a Monte Carlo search for zeolite-like materials. Positions of Si atoms as well as unit cell, space group, density, and number of crystallographically unique atoms were explored in the construction of this database. The database contains over 2.6 M unique structures. Roughly 15% of these are within +30 kJ mol(-1) Si of α-quartz, the band in which most of the known zeolites lie. These structures have topological, geometrical, and diffraction characteristics that are similar to those of known zeolites. The database is the result of refinement by two interatomic potentials that both satisfy the Pauli exclusion principle. The database has been deposited in the publicly available PCOD database and in www.hypotheticalzeolites.net/database/deem/. This journal is © the Owner Societies 2011

Chemical data and variation diagrams of igneous rocks from the Timber Mountain-Oasis Valley Caldera Complex, southern Nevada

USGS Publications Warehouse

Quinlivan, W.D.; Byers, F.M.

1977-01-01

Silica variation diagrams presented here are based on 162 chemical analyses of tuffs, lavas, and intrusives, representative of volcanic centers of the Timber Mountain-Oasis Valley caldera complex and cogenetic rocks of the Silent Canyon ca1dera. Most of the volcanic units sampled are shown on the U.S. Geological Survey geologic map of the Timber Mountain caldera area (I-891) and are described in U.S. Geological Survey Professional Paper 919. Early effusives of the complex, although slightly altered, are probably chemically, and petrographically, more like the calc-alkalic Fraction Tuff (Miocene) of the northern Nellis Air Force Base Bombing and Gunnery Range to the north, whereas effusives of later Miocene age, such as the Paintbrush and Timber Mountain Tuffs, are alkali-calcic.

Characteristics of Fault Zones in Volcanic Rocks Near Yucca Flat, Nevada Test Site, Nevada

USGS Publications Warehouse

Sweetkind, Donald S.; Drake II, Ronald M.

2007-01-01

During 2005 and 2006, the USGS conducted geological studies of fault zones at surface outcrops at the Nevada Test Site. The objectives of these studies were to characterize fault geometry, identify the presence of fault splays, and understand the width and internal architecture of fault zones. Geologic investigations were conducted at surface exposures in upland areas adjacent to Yucca Flat, a basin in the northeastern part of the Nevada Test Site; these data serve as control points for the interpretation of the subsurface data collected at Yucca Flat by other USGS scientists. Fault zones in volcanic rocks near Yucca Flat differ in character and width as a result of differences in the degree of welding and alteration of the protolith, and amount of fault offset. Fault-related damage zones tend to scale with fault offset; damage zones associated with large-offset faults (>100 m) are many tens of meters wide, whereas damage zones associated with smaller-offset faults are generally a only a meter or two wide. Zeolitically-altered tuff develops moderate-sized damage zones whereas vitric nonwelded, bedded and airfall tuff have very minor damage zones, often consisting of the fault zone itself as a deformation band, with minor fault effect to the surrounding rock mass. These differences in fault geometry and fault zone architecture in surface analog sites can serve as a guide toward interpretation of high-resolution subsurface geophysical results from Yucca Flat.

Chemical evolution of a pleistocene rhyolitic center: Sierra La Primavera, Jalisco, México

NASA Astrophysics Data System (ADS)

Mahood, Gail A.

1981-06-01

The late Pleistocene caldera complex of the Sierra La Primavera, Jalisco, México, contains well-exposed lava flows and domes, ash-flow tuff, air-fall pumice, and caldera-lake sediments. All eruptive units are high-silica rhyolites, but systematic chemical differences correlate with age and eruptive mode. The caldera-producing unit, the 45-km3 Tala Tuff, is zoned from a mildly peralkaline first-erupted portion enriched in Na, Rb, Cs, Cl, F, Zn, Y, Zr, Hf, Ta, Nb, Sb, HREE, Pb, Th, and U to a metaluminous last-erupted part enriched in K, LREE, Sc, and Ti; Al, Ca, Mg, Mn, Fe, and Eu are constant within analytical errors. The earliest post-caldera lava, the south-central dome, is nearly identical to the last-erupted portion of the Tala Tuff, whereas the slightly younger north-central dome is chemically transitional from the south-central dome to later, moremafic, ring domes. This sequence of ash-flow tuff and domes represents the tapping of progressively deeper levels of a zoned magma chamber 95,000 ± 5,000 years ago. Since that time, the lavas that erupted 75,000, 60,000, and 30,000 years ago have become decreasingly peralkaline and progressively enriched only in Si, Rb, Cs, and possibly U. They represent successive eruption of the uppermost magma in the post-95,000-year magma chamber. Eruptive units of La Primavera are either aphyric or contain up to 15% phenocrysts of sodic sanidine ≧quartz >ferrohedenbergite >fayalite>ilmenite±titanomagnetite. Whereas major-element compositions of sanidine, clinopyroxene, and fayalite phenocrysts changed only slightly between eruptive groups, concentrations of many trace elements changed by factors of 5 to 10, resulting in crystal/glass partition coefficients that differ by factors of up to 20 between successively erupted units. The extreme variations in partitioning behavior are attributed to small changes in bulk composition of the melt because major-element compositions of the phenocrysts and temperature, pressure, and oxygen fugacity of the magma all remained essentially constant. Crystal settling and incremental partial melting by themselves appear incapable of producing either the chemical gradients within the Tala Tuff magma chamber or the trends with time in the post-caldera lavas. Transport of trace metals as volatile complexes within the thermal and gravitational gradient in volatilerich but water-undersaturated magma is considered the dominant process responsible for compositional zonation in the Tala Tuff. The evolution of the post-caldera lavas with time is thought to involve the diffusive emigration of trace elements from a relatively dry magma as a decreasing proportion of network modifiers and/or a decreasing concentration of complexing ligands progressively reduced trace-metal-site availability in the silicate melt.

Paleomagnetism and Lithostratigraphy of the Miocene Tuff of Huntoon Creek Type Section

NASA Astrophysics Data System (ADS)

Johnson, S.; Pluhar, C. J.; Lindeman, J. R.

2014-12-01

Here we define the Tuff of Huntoon Creek (THC), previously identified and mapped in Mono Basin, CA by Gilbert et al. (1968) as "latite ignimbrite" (K-Ar date of 11.1-11.9 Ma). Formally defining this formation and its paleomagnetic characteristics, can help reveal the spatial and temporal relationships of the Walker Lane and Mina Deflection structural features, including distribution of vertical axis rotation. THC is composed of four tuffs with an intercalated volcaniclastic sandstone giving a total stratigraphic thickness of ~300 m. We define THC in a gorge of Huntoon Creek, where the stratigraphic section is capped by Pliocene basalt. The lowest and most extensive stratigraphic unit, the Huntoon Valley member of THC, is ~243 m thick and can be distinguished from other units by the presence of sanidine and biotite phenocrysts and normal polarity. A 7-meter-thick volcaniclastic sandstone overlies the Huntoon Valley member, straddling a magnetic polarity reversal within the section. The 3 overlying members of THC are reversed-polarity, biotite-bearing, sanidine-free tuffs of variable degrees of welding. Their paleomagnetic directions are each statistically distinguishable from the others, indicating that the deposition of each tuff is separated by a significant amount of time and can be used as a geologically instantaneous measure of Earth's magnetic field for purposes of averaging out secular variation. The capping Pliocene olivine basalt was emplaced over an erosional unconformity of significant relief, as evidenced by the complete absence at some locations of the uppermost biotite-bearing THC member. The tilt corrected mean paleomagnetic direction for the 4 members of THC indicate a clockwise rotation magnitude of 77.5°±40.3°. The absolute rotation results of this locality are statistically indistinguishable from the relative rotation results of this locality compared to Cowtrack Mountain (Lindeman et al. 2013). The corroboration of these data suggests that this region of the Mina Deflection has undergone large magnitude clockwise rotation since the emplacement of THC. However, the capping basalt exhibits a magnetic declination of due north, suggesting that this unit experienced little rotation and that rotational deformation in this region had mostly ended by the time of its emplacement at ~3.5 Ma.

Generation of Continental Crust in Central America: New Field and Geochemical Observations on Silicic Magmatism in Costa Rica

NASA Astrophysics Data System (ADS)

Szymanski, D. W.; Patino, L. C.; Vogel, T. A.; Alvarado, G. E.

2002-12-01

Explaining the occurrence of high-silica arc magmatism in the absence of continental crust remains a fundamental problem in igneous petrology. Recent work in the southern portion of the Central American volcanic arc has expanded the database for the abundant high-silica ash-flow tuffs erupted on top of thick oceanic basement in Costa Rica and southern Nicaragua. Regional differences in geochemistry are observed in data from central and northern Costa Rica. In addition, local heterogeneities among units are demonstrated in plots of both major and trace elements. High-silica ash-flow tuffs in central Costa Rica include the Tiribi Tuff (~0.33 Ma) and Alto Palomo formation (~0.56 Ma). In northern Costa Rica, numerous large silicic ash-flow sheets are found in the Guanacaste province, ranging from late Miocene (<10 Ma) to Pleistocene (~0.6 Ma) in age. A frequency histogram of normalized silica content for all analyses to date from these units (n=222) produces a left-skewed curve with a mode occurring at approximately 70 wt.% SiO2. Samples from the northern region (n=107) demonstrate a tighter distribution of silica content (60.1-78.7 wt.% SiO2 with a median of 72.2 wt.% SiO2) compared to samples from the central region (n=115, 55.4-74.2 wt.% SiO2 with a median of 67.1 wt.% SiO2). The least evolved samples come from the Tiribi Formation in the Valle Central and are chemically distinct from rocks in the Guanacaste region. In both chemistry and geographical position, the Alto Palomo formation appears to represent a transition between tuffs in the Valle Central and those in Guanacaste. Incompatible trace element ratios for these units are nearly identical to regional trends observed in basaltic to andesitic lavas of the modern Costa Rican arc (e.g. Ba/Nb). The Papagayo sequence is an example of chemical variation within one vertical section. The sequence is a ~21 m section of well-exposed tuff that represents an essentially continuous sampling of an evolving magma body. Major-element analyses from a systematic vertical sampling of the section support a model of crystal fractionation, eruption, and mafic replenishment of the magma chamber. Samples range from 60.1 to 70.2 wt.% SiO2, with the most mafic sample occurring at the top of sequence as a visibly mafic-silicic mingled pumice. The Rio Liberia (~1.47 Ma) and Salitral (~1.3 Ma) formations in the Guanacaste region form a series of tuffs, related by the same inferred vent. Despite overlapping silica content, the units have distinct mineral compositions. The Salitral formation includes plagioclase- and amphibole-rich units that appear very similar in the field, while the Rio Liberia contains biotite. Chemically, the units are distinct, forming several separate trends in trace element plots. These heterogeneities most likely reflect differences in both source and/or processes of magma evolution.

A Remotely Sensed and Paleomagnetic Perspective on the Bonelli Tuff of NW AZ and SE CA

NASA Astrophysics Data System (ADS)

Gomez, C. D.

2015-12-01

The southern Black and Cerbat Mountains of NW AZ and the Sacramento Mountains of SE CA preserve ignimbrites associated with multiple episodes of volcanic activity that span at least a million years. Unraveling the stratrigraphy of these deposits, as well as their eruptive centers, is critical for constraining the volcanic history of this ignimbrite, the 18.8 Ma Peach Spring Tuff, is the recently identified 17.7 Ma Tuff of Bonelli House (TB) (Ferguson & Cook 2015) and may also occur in the southern Black and Sacramento Mountains. To help determine the extent and possible source of the TB, we have performed a combined remote sensing and paleomagnetic study of this unit, including possible correlatives. Paleomagnetic work involved Remanence and anisotropic magnetic susceptibility methods. Drill samples were collected and processed at Scripps Institute of Oceanography & Pomona College. An AC current was run to obtain the Paleomag current, as opposed to the traditional of heating up the cores at specific intervals. Sacramento Mountains samples produced an average direction of 200.9 / -26.4, which contrasts the Peach Spring Tuff paleodirection of 036.4/33 (Wells & Hillhouse, 1989). An AMS direction was determined using a MFK1 Kappabridge instrument and consistently showed similar flow direction to that of the PST. In compiling our data on a map, we took into account the Whipple Detachment Fault, ~40 km westward (Lister & Davis, 1989). We were able to identify a spectral signature and remnant paleomagnetic direction for the TB and identify potential additional outcrops in the southern Black mountains. AMS showed us that the ignimbrites originated from a source in the Silver Creek Caldera, which may indicate the PST at TB were produced from a similar source. The remnant paleomagnetic direction allows us to closely correlate these tuff units as occurring within a similar timeframe. The contrasting paleodirection of the TB and the PST allows us to confidently say that the Peach Spring and Bonelli Tuffs occurred at different times when the Earth's magnetic field directions were different.

Stochastic Model of Fracture Frequency Heterogeneity in a Welded Tuff EGS reservoir, Snake River Plain, Idaho, USA

NASA Astrophysics Data System (ADS)

Moody, A.; Fairley, J. P., Jr.

2014-12-01

In light of recent advancements in reservoir enhancement and injection tests at active geothermal fields, there is interest in investigating the geothermal potential of widespread subsurface welded tuffs related to caldera collapse on the Snake River Plain (SRP). Before considering stimulation strategies, simulating heat extraction from the reservoir under in-situ fracture geometries will give a first-order estimation of extractable heat. With only limited deep boreholes drilled on the SRP, few analyses of the bulk hydrologic properties of the tuffs exist. Acknowledging the importance of the spatial heterogeneity of fractures to the permeability and injectivity of reservoirs hosted in impermeable volcanic units, we present fracture distributions from ICDP hole 5036-2A drilled as a part of Project HOTSPOT. The core documents more than 1200 m of largely homogeneous densely welded tuff hosting an isothermal warm-water reservoir at ~60˚ C. Multiple realizations of a hypothetical reservoir are created using sequential indicator algorithms that honor the observed vertical fracture frequency statistics. Results help form criteria for producing geothermal energy from the SRP.

IM-16: A new microporous germanosilicate with a novel framework topology containing d4r and mtw composite building units

DOE Office of Scientific and Technical Information (OSTI.GOV)

Lorgouilloux, Yannick; Dodin, Mathias; Paillaud, Jean-Louis

2009-03-15

The synthesis and the structure of IM-16 a new germanosilicate with a novel zeolitic topology prepared hydrothermally with the ionic liquid 3-ethyl-1-methyl-3H-imidazol-1-ium as the organic structure-directing agent are reported. The structure of calcined and partially rehydrated IM-16 of chemical formula |(H{sub 2}O){sub 0.16}|[Si{sub 3.47}Ge{sub 2.53}O{sub 12}] was solved from powder XRD data in space group Cmcm with a=15.0861(2) A, b=17.7719(3) A, c=19.9764(3) A, V=5355.84(12) A{sup 3} (Z=16). This new zeolite framework type contains 10-MRs channels and may be described from the d4r and mtw composite building units. - Graphical abstract: The synthesis and the structure of IM-16 a new germanosilicatemore » with a novel zeolitic topology prepared hydrothermally with the ionic liquid 3-ethyl-1-methyl-3H-imidazol-1-ium as the organic structure-directing agent are reported. This new zeolite framework type contains 10-MRs channels and may be described from the d4r and mtw composite building units.« less

Zeolite A imidazolate frameworks

NASA Astrophysics Data System (ADS)

Hayashi, Hideki; Côté, Adrien P.; Furukawa, Hiroyasu; O'Keeffe, Michael; Yaghi, Omar M.

2007-07-01

Faujasite (FAU) and zeolite A (LTA) are technologically important porous zeolites (aluminosilicates) because of their extensive use in petroleum cracking and water softening. Introducing organic units and transition metals into the backbone of these types of zeolite allows us to expand their pore structures, enhance their functionality and access new applications. The invention of metal-organic frameworks and zeolitic imidazolate frameworks (ZIFs) has provided materials based on simple zeolite structures where only one type of cage is present. However, so far, no metal-organic analogues based on FAU or LTA topologies exist owing to the difficulty imposed by the presence of two types of large cage (super- and β-cages for FAU, α- and β-cages for LTA). Here, we have identified a strategy to produce an LTA imidazolate framework in which both the link geometry and link-link interactions play a decisive structure-directing role. We describe the synthesis and crystal structures of three porous ZIFs that are expanded analogues of zeolite A; their cage walls are functionalized, and their metal ions can be changed without changing the underlying LTA topology. Hydrogen, methane, carbon dioxide and argon gas adsorption isotherms are reported and the selectivity of this material for carbon dioxide over methane is demonstrated.

Zeolite A imidazolate frameworks.

PubMed

Hayashi, Hideki; Côté, Adrien P; Furukawa, Hiroyasu; O'Keeffe, Michael; Yaghi, Omar M

2007-07-01

Faujasite (FAU) and zeolite A (LTA) are technologically important porous zeolites (aluminosilicates) because of their extensive use in petroleum cracking and water softening. Introducing organic units and transition metals into the backbone of these types of zeolite allows us to expand their pore structures, enhance their functionality and access new applications. The invention of metal-organic frameworks and zeolitic imidazolate frameworks (ZIFs) has provided materials based on simple zeolite structures where only one type of cage is present. However, so far, no metal-organic analogues based on FAU or LTA topologies exist owing to the difficulty imposed by the presence of two types of large cage (super- and beta-cages for FAU, alpha- and beta-cages for LTA). Here, we have identified a strategy to produce an LTA imidazolate framework in which both the link geometry and link-link interactions play a decisive structure-directing role. We describe the synthesis and crystal structures of three porous ZIFs that are expanded analogues of zeolite A; their cage walls are functionalized, and their metal ions can be changed without changing the underlying LTA topology. Hydrogen, methane, carbon dioxide and argon gas adsorption isotherms are reported and the selectivity of this material for carbon dioxide over methane is demonstrated.

Physical and Thermal Structure of the Bishop Tuff, California

NASA Astrophysics Data System (ADS)

Wilson, C. J.; Hildreth, W.

2001-12-01

The 0.76 Ma Bishop Tuff, California, includes an ignimbrite constructed from a series of overlapping packages of material erupted sequentially and simultaneously from multiple sources around the ring fracture of Long Valley caldera (Wilson, C.J.N., Hildreth, W., 1997, Journal of Geology 105, 407-439). Exceptionally good continuous exposures of the ignimbrite in the walls of Owens Gorge to the east of Long Valley provide a cross-section through the east-side packages (Ig1E and Ig2E). We have measured 10 sections up the gorge walls to draw up a cross section of the ignimbrite down Owens Gorge, using lithic abundances and lithologies to define the physical eruptive packages and their subdivisions, and measurements of tuff bulk density (as an easily measured proxy for welding intensity) to define the thermal eruptive packages. The physically emplaced bodies of ignimbrite represent an overlapping, shingling suite of material such that successively later ignimbrite occurs most prominently farther away from source. Two major and two lesser zones of maximum density (welding) are present, the lower two (in Ig1Ea and lower Ig1Eb) in upper Owens Gorge, and the two most prominent (upper Ig1Eb and Ig2Eb) in middle and lower parts of the gorge. Welding fluctuations are controlled by bulk temperatures of individual batches of hotter and cooler material, but the intensity of the welding also depends on deposit thickness (i.e. load stress). Physically defined contacts between ignimbrite packages show that time breaks inferred to be of hours may not result in formation of any visible parting or flow unit boundary. Furthermore, positions of density (welding) minima between zones of higher density tuff do not coincide with horizons of stratigraphic significance. These observations lead to two conclusions. (1) The absence of clear partings or flow unit boundaries in an ignimbrite sequence is not diagnostic either of the material representing a single flow unit, or of the material being continuously progressively aggraded. (2) Use of the density (welding) minimum to locate the boundaries of cooling units and in measuring and modelling the emplacement and thermal history of compound cooling units may lead to errors.

Paleoflow of the Tuff of San Felipe on Isla Angel de la Guarda

NASA Astrophysics Data System (ADS)

Skinner, S. M.; Stock, J. M.; Martin Barajas, A.

2013-05-01

The Tuff of San Felipe is a widespread 12.5 Ma ignimbrite in northwestern Mexico that has a proven potential in reconstructing the rifting history of the Gulf of California. Previous studies have used the Tuff of San Felipe to correlate Isla Tiburon to the Sierra San Felipe on the Baja California Peninsula, and to correlate central Isla Angel de la Guarda to Baja California in the region of Cataviña. However, because only scattered outcrops are preserved in this latter region, paleoflow directions are an important additional constraint for reconstructing its past position relative to Isla Angel de la Guarda. We have confirmed the presence of the Tuff of San Felipe on Isla Angel de la Guarda and collected rocks from 44 sites for paleomagnetic and AMS analysis. Our work on the Tuff of San Felipe has revealed discrepancies in the magnetic fabric, and resulting flow direction, on the scale of hundreds of meters. The lack of a uniform flow direction from a single mesa impairs our ability to correlate offset channelized flows over large distances. To investigate the robustness of the AMS fabric we have performed a spatially dense sampling of the unit. Rigorous rock magnetic experiments will be used to investigate any correlation between changes in the magnetic mineralogy of the samples and any irregularities or constancies in the measured fabrics and flow directions. With this study we aim to characterize the variability of the AMS ellipsoid in natural volcanic samples and the scale at which AMS can be used as a meaningful indicator of paleoflow in the Tuff of San Felipe.

Trondhjemite and metamorphosed quartz keratophyre tuff of the Ammonoosuc volcanics (Ordovician), western New Hampshire and adjacent Vermont and Massachusetts.

USGS Publications Warehouse

Leo, G.W.

1985-01-01

These volcanic rocks consist of a lower, mainly mafic unit of hornblende-plagioclase amphibolite and an upper, mainly felsic metamorphosed quartz keratophyre tuff. They are intruded by sills, dykes and plugs of trondhjemite; which is highly silicic (SiO2, 73-81%), low in Al2O3 (11.3-13.5%) and generally contains <1% K2O. Both trondhjemite and volcanics are calc-alkaline. The major- and minor-element geochemistry of the trondhjemites is closely similar to that of the quartz keratophyre tuff. These rocks were probably produced by partial melting of basaltic source rocks, rather than by fractional crystallization, in view of the virtually bimodal nature of the Ammonoosuc assemblage. The generation of the felsic rocks occurred at deeper levels along a subduction zone dipping eastward.-L.C.H.

The effect of positioning cations on acidity and stability of the framework structure of Y zeolite

PubMed Central

Deng, Changshun; Zhang, Junji; Dong, Lihui; Huang, Meina; Bin Li; Jin, Guangzhou; Gao, Junbin; Zhang, Feiyue; Fan, Minguang; Zhang, Luoming; Gong, Yanjun

2016-01-01

The investigation on the modification of NaY zeolite on LaHY and AEHY (AE refers Ca and Sr and the molar ratio of Ca and Sr is 1:1) zeolites was proformed by XRD, N2-physisorption (BET), XRF, XPS, NH3-TPD, Py-IR, hydrothermal stability, and catalytic cracking test. These results indicate that HY zeolite with ultra low content Na can be obtained from NaY zeolite through four exchange four calcination method. The positioning capability of La3+ in sodalite cage is much better than that of AE2+ and about 12 La3+ can be well coordinated in sodalite cages of one unit cell of Y zeolite. Appropriate acid amount and strength favor the formation of propylene and La3+ is more suitable for the catalytic cracking of cyclohexane than that of AE2+. Our results not only elaborate the variation of the strong and weak acid sites as well as the Brönsted and Lewis acid sites with the change of exchanged ion content but also explore the influence of hydrothermal aging of LaHY and AEHY zeolites and find the optimum ion exchange content for the most reserved acid sites. At last, the coordination state and stabilization of ion exchanged Y zeolites were discussed in detail. PMID:26987306

New approach for determination of the influence of long-range order and selected ring oscillations on IR spectra in zeolites

NASA Astrophysics Data System (ADS)

Mikuła, Andrzej; Król, Magdalena; Mozgawa, Włodzimierz; Koleżyński, Andrzej

2018-04-01

Vibrational spectroscopy can be considered as one of the most important methods used for structural characterization of various porous aluminosilicate materials, including zeolites. On the other hand, vibrational spectra of zeolites are still difficult to interpret, particularly in the pseudolattice region, where bands related to ring oscillations can be observed. Using combination of theoretical and computational approach, a detailed analysis of these regions of spectra is possible; such analysis should be, however, carried out employing models with different level of complexity and simultaneously the same theory level. In this work, an attempt was made to identify ring oscillations in vibrational spectra of selected zeolite structures. A series of ab initio calculations focused on S4R, S6R, and as a novelty, 5-1 isolated clusters, as well as periodic siliceous frameworks built from those building units (ferrierite (FER), mordenite (MOR) and heulandite (HEU) type) have been carried out. Due to the hierarchical structure of zeolite frameworks it can be expected that the total envelope of the zeolite spectra should be with good accuracy a sum of the spectra of structural elements that build each zeolite framework. Based on the results of HF calculations, normal vibrations have been visualized and detailed analysis of pseudolattice range of resulting theoretical spectra have been carried out. Obtained results have been applied for interpretation of experimental spectra of selected zeolites.

New 40Ar/39Ar age of the Bishop Tuff from multiple sites and sediment rate calibration for the Matuyama-Brunhes boundary

USGS Publications Warehouse

Sarna-Wojcicki, A. M.; Pringle, M.S.; Wijbrans, J.

2000-01-01

Precise dating of sanidine from proximal ash flow Bishop Tuff and air fall Bishop pumice and ash, California, can be used to derive an absolute age of the Matuyama Reversed-Brunhes Normal (M-B) paleomagnetic transition, identified stratigraphically close beneath the Bishop Tuff and ash at many sites in the western United States. An average age of 758.9 ?? 1.8 ka, standard error of the mean (SEM), was obtained for individual sanidine crystals or groups of several crystals, determined from ???70 individual analyses of sanidine separates from 11 sample groups obtained at five localities. The basal air fall pumice (757.7 ?? 1.8 ka) and overlying ash flow tuff (762.2 ?? 4.7 ka) from near the source yield essentially the same dates within errors of analysis, suggesting that the two units were emplaced close in time. A date on distal Bishop air fall ash bed at Friant, California, ???100 km to the west of the source area, is younger, 750.1 ?? 4.3 ka, but not significantly different within analytical error (??1 standard deviation). Previous dates of the Bishop Tuff, obtained by others using conventional K-Ar and the fission track method on zircons, ranged from ???650 ka to ???1.0 Ma. The most recent, generally accepted date by the K-Ar method on sanidine was 738 ?? 3 ka. We infer, as others before, that many K-Ar dates on sanidine feldspar are too young owing to incomplete degassing of radiogenic Ar during fusion in the K-Ar technique and that many older K-Ar dates are too old owing to detrital or xenocrystic contamination in the larger samples that are necessary for the technique. The new dates are similar to recent 40Ar/39Ar ages of the Bishop Tuff determined on individual samples by others but are derived from a larger proximal sample population and from multiple analysis of each sample. The results provide a definitive and precise age calibration of this widespread chronostratigraphic marker in the western United States and northeastern Pacific Ocean. We calculated the age of the M-B transition at five sites, assuming constant sedimentation rates, the age of the Bishop ash bed and one or more well-dated chronostratigraphic horizons above and below the Bishop Tuff ash bed and M-B transition, and stratigraphic separations between these datum levels. The age of the M-B transition is 774.2 ?? 2.8 ka, based on the average of eight such calculations, close to other recent determinations, and similar to that determined from the astronomically tuned polarity timescale. Our approach provides an alternative and surprisingly precise method for determining the age of the M-B and other chronostratigraphic levels. The above dates, calculated using U.S. Geological Survey values of 27.92 Ma for the Taylor Creek (TC) sanidine can be recalculated to other widely used values for these monitors. For example, using recently published values of 28.34 Ma (TC) and 523.1 Ma (McLure Mountain hornblende, MMhb-1), the resulting ages are ???774 ka for the Bishop Tuff and ash bed and ???789 ka for the M-B transition. Copyright 2000 by the American Geophysical Union.

Stratigraphy, correlation, depositional setting, and geophysical characteristics of the Oligocene Snowshoe Mountain Tuff and Creede Formation in two cored boreholes

USGS Publications Warehouse

Larsen, Daniel; Nelson, Philip H.

2000-01-01

Core descriptions and geophysical logs from two boreholes (CCM-1 and CCM-2) in the Oligocene Snowshoe Mountain Tuff and Creede Formation, south-central Colorado, are used to interpret sedimentary and volcanic facies associations and their physical properties. The seven facies association include a mixed sequence of intracaldera ash-flow tuffs and breccias, alluvial and lake margin deposits, and tuffaceous lake beds. These deposits represent volcanic units related to caldera collapse and emplacement of the Snowshoe Mountain Tuff, and sediments and pyroclastic material deposited in the newly formed caldera basin, Early sedimentation is interpreted to have been rapid, and to have occurred in volcaniclastic fan environments at CCM-1 and in a variery of volcaniclastic fan, braided stream shallow lacustrine, and mudflat environments at CCM-2. After an initial period of lake-level rise, suspension settling, turbidite, and debris-flow sedimentation occurred in lacustrine slope and basin environments below wave base. Carbonate sedimentation was initially sporadic, but more continuous in the latter part of the recorded lake history (after the H fallout tuff). Sublacustrine-fan deposition occurred at CCM-1 after a pronounced lake-level fall and subsequent rise that preceded the H tuff. Variations in density, neutron, gamma-ray, sonic, and electrical properties of deposits penetrated oin the two holes reflect variations in lithology, porosity, and alteration. Trends in the geophysical properties of the lacustrine strata are linked to downhole changes in authigenic mineralology and a decrease in porosity interpreted to have resulted primarily from diagenesis. Lithological and geophysical characteristics provide a basis for correlation of the cores; however, mineralogical methods of correlation are hampered by the degree of diagenesis and alteration.

Paleoflow of the Tuff of San Felipe on Isla Angel de la Guarda

NASA Astrophysics Data System (ADS)

Skinner, S. M.; Stock, J. M.; Martin, A.

2013-12-01

The Tuff of San Felipe is a widespread 12.5 Ma ignimbrite in northwestern Mexico that has a proven potential in reconstructing the rifting history of the Gulf of California. Previous studies have used the Tuff of San Felipe to correlate Isla Tiburon to the Sierra San Felipe on the Baja California Peninsula, and to correlate central Isla Angel de la Guarda to Baja California in the region of Cataviña. However, because only scattered outcrops are preserved in this latter region, paleoflow directions are an important additional constraint for reconstructing its past position relative to Isla Angel de la Guarda. We have confirmed the presence of the Tuff of San Felipe on Isla Angel de la Guarda and collected rocks from 44 sites for paleomagnetic and AMS analysis. Our work on the Tuff of San Felipe has revealed discrepancies in the magnetic fabric, and resulting flow direction. The azimuth of flow directions observed at 27 sites over 1.5 square kilometers ranges from 8° to 355° with a mean direction of 195° and an α95 of 27°. The lack of a uniform flow direction from a single mesa impairs our ability to correlate offset channelized flows over large distances. To investigate the robustness of the AMS fabric we have performed a spatially dense sampling of the unit. Rigorous rock magnetic experiments will be used to investigate any correlation between changes in the magnetic mineralogy of the samples and any irregularities or constancies in the measured fabrics and flow directions. With this study we aim to characterize the variability of the AMS ellipsoid in natural volcanic samples and the scale at which AMS can be used as a meaningful indicator of paleoflow in the Tuff of San Felipe.

Vegetation during UMBI and deposition of Tuff IF at Olduvai Gorge, Tanzania (ca. 1.8 Ma) based on phytoliths and plant remains.

PubMed

Albert, Rosa Maria; Bamford, Marion K

2012-08-01

As part of ongoing research at Olduvai Gorge, Tanzania, to determine the detailed paleoenvironmental setting during Bed I and Bed II times and occupation of the basin by early hominins, we present the results of phytolith analyses of Tuff IF which is the uppermost unit of Bed I. Phytoliths were identified in most of the levels and localities on the eastern paleolake margin, but there are not always sufficient numbers of identifiable morphologies to infer the specific type of vegetation due to dissolution. Some surge surfaces and reworked tuff surfaces were vegetated between successive ash falls, as indicated by root-markings and the presence of a variety of phytolith morphotypes. Dicotyledonous wood/bark types were dominant except at the FLK N site just above Tuff IF when monocots are dominant and for the palm-dominated sample from the reworked channel cutting down into Tuff IF at FLK N. The area between the two fault scarps bounding the HWK Compartment, approximately 1 km wide, was vegetated at various time intervals between some of the surges and during the reworking of the Tuff. By lowermost Bed II times the eastern margin was fully vegetated again. Climate and tectonic activity probably controlled the fluctuating lake levels but locally the paleorelief and drainage were probably the controlling factors for the vegetation changes. These data support a scenario of small groups of hominins making brief visits to the paleolake during uppermost Bed I times, followed by a more desirable vegetative environment during lowermost Bed II times. Copyright © 2011 Elsevier Ltd. All rights reserved.

Extra-large pore zeolite (ITQ-40) with the lowest framework density containing double four- and double three-rings

PubMed Central

Díaz-Cabañas, M. J.; Jiang, J.; Afeworki, M.; Dorset, D. L.; Soled, S. L.; Strohmaier, K. G.

2010-01-01

The first zeolite structure (ITQ-40) that contains double four (D4) and double three (D3) member ring secondary building units has been synthesized by introducing Ge and NH4F and working in concentrated synthesis gels. It is the first time that D3-Rs have been observed in a zeolite structure. As was previously analyzed [Brunner GO, Meier, WM (1989) Nature 337:146–147], such a structure has a very low framework density (10.1 T/1,000 Å3). Indeed, ITQ-40 has the lowest framework density ever achieved in oxygen-containing zeolites. Furthermore, it contains large pore openings, i.e., 15-member rings parallel to the [001] hexagonal axis and 16-member ring channels perpendicular to this axis. The results presented here push ahead the possibilities of zeolites for uses in electronics, control delivery of drugs and chemicals, as well as for catalysis. PMID:20660773

New seismo-stratigraphic and marine magnetic data of the Gulf of Pozzuoli (Naples Bay, Tyrrhenian Sea, Italy): inferences for the tectonic and magmatic events of the Phlegrean Fields volcanic complex (Campania)

NASA Astrophysics Data System (ADS)

Aiello, Gemma; Marsella, Ennio; Fiore, Vincenzo Di

2012-06-01

A detailed reconstruction of the stratigraphic and tectonic setting of the Gulf of Pozzuoli (Naples Bay) is provided on the basis of newly acquired single channel seismic profiles coupled with already recorded marine magnetics gathering the volcanic nature of some seismic units. Inferences for the tectonic and magmatic setting of the Phlegrean Fields volcanic complex, a volcanic district surrounding the western part of the Gulf of Naples, where volcanism has been active since at least 50 ka, are also discussed. The Gulf of Pozzuoli represents the submerged border of the Phlegrean caldera, resulting from the volcano-tectonic collapse induced from the pyroclastic flow deposits of the Campanian Ignimbrite (35 ka). Several morpho-depositional units have been identified, i.e., the inner continental shelf, the central basin, the submerged volcanic banks and the outer continental shelf. The stratigraphic relationships between the Quaternary volcanic units related to the offshore caldera border and the overlying deposits of the Late Quaternary depositional sequence in the Gulf of Pozzuoli have been highlighted. Fourteen main seismic units, both volcanic and sedimentary, tectonically controlled due to contemporaneous folding and normal faulting have been revealed by geological interpretation. Volcanic dykes, characterized by acoustically transparent sub-vertical bodies, locally bounded by normal faults, testify to the magma uprising in correspondence with extensional structures. A large field of tuff cones interlayered with marine deposits off the island of Nisida, on the western rim of the gulf, is related to the emplacement of the Neapolitan Yellow Tuff deposits. A thick volcanic unit, exposed over a large area off the Capo Miseno volcanic edifice is connected with the Bacoli-Isola Pennata-Capo Miseno yellow tuffs, cropping out in the northern Phlegrean Fields.

Antibacterial properties of Ag-exchanged Philippine natural zeolite-chitosan composites

NASA Astrophysics Data System (ADS)

Taaca, Kathrina Lois M.; Olegario, Eleanor M.; Vasquez, Magdaleno R.

2017-12-01

Zeolites are microporous minerals composed of silicon, aluminum and oxygen. These aluminosilicates consist of tetrahedral units which produce open framework structures to generate a system of pores and cavities of molecular dimensions. Zeolites are naturally abundant and can be mined in most parts of the world. In this study, natural zeolites (NaZ) which are locally-sourced here in the Philippines were investigated to determine its properties. An ion-exchange process was utilized, using the zeolite to silver (Ag) solution ratio of 1:20 (w/v), to incorporate Ag into the zeolite framework. Characterizations such as XRD, AAS, and Agar diffusion assay were used to evaluate the properties of the synthesized Ag-exchanged zeolites (AgZ). X-ray diffraction revealed that both NaZ and AgZ have peaks mostly corresponding to the clinoptilolite structure, with some trace peaks of the mordenite and quartz. Absorption spectroscopy revealed that the ion exchange process added about 0.61188g of silver into the zeolite structure. This Ag content was seen to be enough to make the AgZ sample exhibit an antibacterial effect where clearing zones against E. coli and S. aureus were observed in the agar diffusion assay, respectively. The AgZ sample was also tested as ceramic filler to a polymer matrix-chitosan. The diffusion assay revealed presence of antibacterial activity to the polymer composite with AgZ fillers. These results indicate that the Philippine natural zeolite, incorporated with metals such as Ag, can be used as an antibacterial agent and can be developed as a ceramic filler to improve the antibacterial property of composite materials for biomedical application.

La roca magica: Uses of natural zeolites in agriculture and industry

PubMed Central

Mumpton, Frederick A.

1999-01-01

For nearly 200 years since their discovery in 1756, geologists considered the zeolite minerals to occur as fairly large crystals in the vugs and cavities of basalts and other traprock formations. Here, they were prized by mineral collectors, but their small abundance and polymineralic nature defied commercial exploitation. As the synthetic zeolite (molecular sieve) business began to take hold in the late 1950s, huge beds of zeolite-rich sediments, formed by the alteration of volcanic ash (glass) in lake and marine waters, were discovered in the western United States and elsewhere in the world. These beds were found to contain as much as 95% of a single zeolite; they were generally flat-lying and easily mined by surface methods. The properties of these low-cost natural materials mimicked those of many of their synthetic counterparts, and considerable effort has made since that time to develop applications for them based on their unique adsorption, cation-exchange, dehydration–rehydration, and catalytic properties. Natural zeolites (i.e., those found in volcanogenic sedimentary rocks) have been and are being used as building stone, as lightweight aggregate and pozzolans in cements and concretes, as filler in paper, in the take-up of Cs and Sr from nuclear waste and fallout, as soil amendments in agronomy and horticulture, in the removal of ammonia from municipal, industrial, and agricultural waste and drinking waters, as energy exchangers in solar refrigerators, as dietary supplements in animal diets, as consumer deodorizers, in pet litters, in taking up ammonia from animal manures, and as ammonia filters in kidney-dialysis units. From their use in construction during Roman times, to their role as hydroponic (zeoponic) substrate for growing plants on space missions, to their recent success in the healing of cuts and wounds, natural zeolites are now considered to be full-fledged mineral commodities, the use of which promise to expand even more in the future. PMID:10097058

Location of MTBE and toluene in the channel system of the zeolite mordenite: Adsorption and host-guest interactions

DOE Office of Scientific and Technical Information (OSTI.GOV)

Arletti, Rossella, E-mail: rossella.arletti@unito.it; Martucci, Annalisa; Alberti, Alberto

This paper reports a study of the location of Methyl Tertiary Butyl Ether (MTBE) and toluene molecules adsorbed in the pores of the organophylic zeolite mordenite from an aqueous solution. The presence of these organic molecules in the zeolite channels was revealed by structure refinement performed by the Rietveld method. About 3 molecules of MTBE and 3.6 molecules of toluene per unit cell were incorporated into the cavities of mordenite, representing 75% and 80% of the total absorption capacity of this zeolite. In both cases a water molecule was localized inside the side pocket of mordenite. The saturation capacity determinedmore » by the adsorption isotherms, obtained by batch experiments, and the weight loss given by thermogravimetric (TG) analyses were in very good agreement with these values. The interatomic distances obtained after the structural refinements suggest MTBE could be connected to the framework through a water molecule, while toluene could be bonded to framework oxygen atoms. The rapid and high adsorption of these hydrocarbons into the organophylic mordenite zeolite makes this cheap and environmental friendly material a suitable candidate for the removal of these pollutants from water. - graphical abstract: Location of MTBE (a) and toluene (b) in mordenite channels (projection along the [001] direction). Highlights: Black-Right-Pointing-Pointer We investigated the MTBE and toluene adsorption process into an organophilic zeolite mordenite. Black-Right-Pointing-Pointer The presence of MTBE and toluene in mordenite was determined by X-ray diffraction studies. Black-Right-Pointing-Pointer About 3 molecules of MTBE and 3.6 molecules of toluene per unit cell were incorporated into the zeolite cavities. Black-Right-Pointing-Pointer MTBE is connected to the framework through a water molecule. Black-Right-Pointing-Pointer Toluene is directly bonded to framework oxygen atoms.« less

La roca magica: uses of natural zeolites in agriculture and industry.

PubMed

Mumpton, F A

1999-03-30

For nearly 200 years since their discovery in 1756, geologists considered the zeolite minerals to occur as fairly large crystals in the vugs and cavities of basalts and other traprock formations. Here, they were prized by mineral collectors, but their small abundance and polymineralic nature defied commercial exploitation. As the synthetic zeolite (molecular sieve) business began to take hold in the late 1950s, huge beds of zeolite-rich sediments, formed by the alteration of volcanic ash (glass) in lake and marine waters, were discovered in the western United States and elsewhere in the world. These beds were found to contain as much as 95% of a single zeolite; they were generally flat-lying and easily mined by surface methods. The properties of these low-cost natural materials mimicked those of many of their synthetic counterparts, and considerable effort has made since that time to develop applications for them based on their unique adsorption, cation-exchange, dehydration-rehydration, and catalytic properties. Natural zeolites (i.e., those found in volcanogenic sedimentary rocks) have been and are being used as building stone, as lightweight aggregate and pozzolans in cements and concretes, as filler in paper, in the take-up of Cs and Sr from nuclear waste and fallout, as soil amendments in agronomy and horticulture, in the removal of ammonia from municipal, industrial, and agricultural waste and drinking waters, as energy exchangers in solar refrigerators, as dietary supplements in animal diets, as consumer deodorizers, in pet litters, in taking up ammonia from animal manures, and as ammonia filters in kidney-dialysis units. From their use in construction during Roman times, to their role as hydroponic (zeoponic) substrate for growing plants on space missions, to their recent success in the healing of cuts and wounds, natural zeolites are now considered to be full-fledged mineral commodities, the use of which promise to expand even more in the future.

Demonstration of a Solar Thermal Combined Heating, Cooling and Hot Water System Utilizing an Adsorption Chiller for DoD Installations

DTIC Science & Technology

2013-12-01

capacities ranging from 3-330 tons using silica gel or 250-450 tons using zeolite desiccant. Adsorption chillers are also currently manufactured by...Mayekawa (20-100 tons using zeolite desiccant) • Union (10-125 tons using silica gel) Sortech - 2 ton units for residential use • InvenSor - 3 ton

A low temperature furnace for solution crystal growth on the International Space Station

NASA Astrophysics Data System (ADS)

Baç, Nurcan; Harpster, Joseph; Maston, Robert A.; Sacco, Albert

2000-01-01

The Zeolite Crystal Growth Furnace Unit (ZCG-FU) is the first module in an integrated payload designed for low temperature crystal growth in solutions on the International Space Station (ISS). This payload is scheduled to fly on the ISS flight 7A.1 in an EXPRESS rack. Its name originated from early shuttle flight experiments limited to the growth of zeolite crystals but has since grown to include other materials of significant commercial interest using the solution method of crystal growth. Zeolites, ferroelectrics, piezeoelectrics and silver halides are some of the materials considered. The ZCG-FU experiment consists of a furnace unit and its electronic control system, and mechanically complex, crystal growth autoclaves suitable for use with a particular furnace and solution. The ZCG facility is being designed to grow into four independent furnaces controlled by IZECS (Improved Zeolite Electronic Control System). IZECS provides monitoring of critical parameters, data logging, safety monitoring, air-to-ground control and operator interfacing. It is suitable for controlling the four furnaces either individually or all at one time. It also contains the power management solid-state drivers and switches for the ZCG-FU furnace. The furnace contains 19 tubes operating at three different temperature zones. .

Relative Abundances of Calcite and Silica in Fracture Coatings as a Possible Indicator of Evaporation in a Thick Unsaturated Zone, Yucca Mountain, Nevada

NASA Astrophysics Data System (ADS)

Marshall, B. D.; Moscati, R. J.

2005-12-01

Yucca Mountain, a ridge of shallowly dipping, Miocene-age volcanic rocks in southwest Nevada, is the proposed site for a nuclear waste repository to be constructed in the 500- to 700-m-thick unsaturated zone (UZ). At the proposed repository, the 300-m-thick Topopah Spring Tuff welded unit (TSw) is overlain by approximately 30 m of nonwelded tuffs (PTn); the Tiva Canyon Tuff welded unit (TCw) overlies the PTn with a range in thickness from 0 to approximately 130 m at the site. The amount of water percolation through the UZ is low and difficult to measure directly, but local seepage into mined tunnels has been observed in the TCw. Past water seepage in the welded tuffs is recorded by widespread, thin (0.3 cm) coatings of calcite and silica on fracture surfaces and within cavities. Abundances of calcite and silica in the coatings were determined by X-ray microfluorescence mapping and subsequent multispectral image analysis of over 200 samples. The images were classified into constituent phases including opal-chalcedony-quartz (secondary silica) and calcite. In the TCw samples, the median calcite/silica ratio is 8; in the TSw samples within 35 m below the PTn, median calcite/silica falls to 2, perhaps reflecting an increase in soluble silica from the presence of glass in the nonwelded tuffs. In the deeper parts of the TSw, median calcite/silica reaches 100 and many samples contain no detectable secondary silica phase. Evaporation and changing pCO2 control precipitation of calcite from water percolating downward in the UZ, but precipitation of opal requires only evaporation. Calcite/silica ratios, therefore, can constrain the relative importance of evaporation in the UZ. Although calcite/silica values scatter widely within the TSw, reflecting the spatial variability of gas and water flow, average calcite/silica ratios increase with stratigraphic depth, indicating less evaporation at the deeper levels of the UZ. Coupled with the much smaller calcite/silica ratios observed in coatings from the TCw, these data indicate that evaporation decreases with depth in the UZ. Evaporation at the repository horizon and in the overlying units is an important process that reduces the amount of seepage at the repository horizon.

Quartz phenocrysts preserve volcanic stresses at Long Valley and Yellowstone calderas

NASA Astrophysics Data System (ADS)

Befus, K. S.; Leonhardi, T. C.; Manga, M.; Tamura, N.; Stan, C. V.

2016-12-01

Magmatic processes and eruptions are the consequence of stresses active in volcanic environments. Few techniques are presently available to quantify those stresses because they operate in subsurface and/or hazardous environments, and thus new techniques are needed to advance our understanding of key processes. Here, we provide a dataset of volcanic stresses that were imparted to quartz crystals that traveled through, and were hosted within, pyroclastic and effusive eruptions from Long Valley and Yellowstone calderas. We measured crystal lattice deformation with submicron spatial resolution using the synchrotron X-ray microdiffraction beamline (12.3.2) at the Advanced Light Source, Lawrence Berkeley National Laboratory. Quartz from all units produces diffraction patterns with residual strains locked in the crystal lattice. We used Hooke's Law and the stiffness constants of quartz to calculate the stresses that caused the preserved residual strains. At Long Valley caldera, quartz preserves stresses of 187±80 MPa within pumice clasts in the F1 fall unit of the Bishop Tuff, and preserves stresses of 120±45 MPa from the Bishop Tuff welded ignimbrite. At Yellowstone caldera quartz preserves stresses of 115±30 and 140±60 MPa within pumices from the basal fall units of the Mesa Falls Tuff and the Tuff of Bluff Point, respectively. Quartz from near-vent and flow-front samples from Summit Lake lava flow preserves stresses up to 130 MPa, and show no variation with distance travelled. We believe that subsurface processes cause the measured residual stresses, but it remains unclear if they are relicts of fragmentation or from the magma chamber. The residual stresses from both Long Valley and Yellowstone samples roughly correlate to lithostatic pressures estimated for the respective pre-eruption magma storage depths. It is possible that residual stress in quartz provides a new geobarometer for crystallization pressure. Moving forward, we will continue to perform analyses and experiments on natural and synthetic crystals to better determine the source of residual stresses.

The Pioneer Ultramafic Complex of the Barberton Greenstone Belt, South Africa

NASA Astrophysics Data System (ADS)

Cooper, M. R.; Byerly, G. R.; Lowe, D. R.; Thompson, M. E.

2005-12-01

The 3.55-3.22 Ga Barberton Greenstone Belt is an approximately 100km x 30km northeast trending, isoclinally folded, volcanic and sedimentary succession surrounded by intrusive granitic rocks. It is perhaps Earth's best preserved mid-Archean supracrustal sequence and also among the most magnesian, making it an ideal location for studying compositionally distinct rocks of the Archean, such as komatiites. The Pioneer Ultramafic Complex has been interpreted as a komatiitic intrusion but we argue that it is a sequence of layered komatiitic flows and interbedded tuffs correlative with other komatiitic extrusive units of the 3.29 Ga Weltevreden Formation, the uppermost formation of the Onverwacht Group. The Pioneer Ultramafic Complex contains at least 900m of section in the study area, including at least 5 flow sets, with individual flows up to 100 m thick, sections of tuff up to 100m thick and additional thinner tuff units. The base of the sequence is in fault contact with the Sawmill Ultramafic Complex, which is similar to and perhaps correlative with the Pioneer. The top of the sequence is bounded by the Moodies Fault and slightly younger sedimentary rocks of the Fig Tree and Moodies Groups. Typical flows of the Pioneer have highly serpentinized olivine-rich cumulate bases, fresh olivine bearing peridotitic lithologies in central portions, and increasing pyroxene content, pyroxene size, and elongation of grains toward the flow tops. Three of the five flows are capped with random and/or oriented spinifex layers. The tuffs within this and other layered ultramafic complexes of the Barberton Greenstone Belt are mostly fine grained, slaty serpentinites that were previously interpreted as bedding horizontal zones of shearing. However, rare preservation of angular and vesicular lapilli, and more commonly cross-stratification in finer grained layers, provide strong evidence that these layers represent tuffs. High chromium and other trace element contents suggest they are komatiitic tuffs likely co-magmatic with the interbedded komatiitic lava flows. Compositions of fresh olivines range between 91 to 93 percent forsterite, indicating a komatiitic melt composition. In addition to olivine phenocrysts, fresh chromite, orthopyroxene, pigeonite, and augite are all present as smaller intercumulus crystals or microphenocrysts. The pyroxenes have Mg numbers up to 89 and Al/Ti ratios approximately 10-15. The latter are consistent with the Al/Ti ratios of 20-30 found within the komatiites and tuffs analyzed thus far. These ratios indicate the flows belong to the aluminium undepleted group of komatiites. The rock and mineral chemistry of these flows allow us to determine melt compositions and explore correlations and relationships with other komatiitic flows and layered ultramafic complexes of the Barberton Greenstone Belt. Field studies of these flows help characterize an Archean igneous complex believed to represent shallow marine deposition of komatiitic tuffs and coeval emplacement of thick vertically differentiated komatiitic flows.

New approach for determination of the influence of long-range order and selected ring oscillations on IR spectra in zeolites.

PubMed

Mikuła, Andrzej; Król, Magdalena; Mozgawa, Włodzimierz; Koleżyński, Andrzej

2018-04-15

Vibrational spectroscopy can be considered as one of the most important methods used for structural characterization of various porous aluminosilicate materials, including zeolites. On the other hand, vibrational spectra of zeolites are still difficult to interpret, particularly in the pseudolattice region, where bands related to ring oscillations can be observed. Using combination of theoretical and computational approach, a detailed analysis of these regions of spectra is possible; such analysis should be, however, carried out employing models with different level of complexity and simultaneously the same theory level. In this work, an attempt was made to identify ring oscillations in vibrational spectra of selected zeolite structures. A series of ab initio calculations focused on S4R, S6R, and as a novelty, 5-1 isolated clusters, as well as periodic siliceous frameworks built from those building units (ferrierite (FER), mordenite (MOR) and heulandite (HEU) type) have been carried out. Due to the hierarchical structure of zeolite frameworks it can be expected that the total envelope of the zeolite spectra should be with good accuracy a sum of the spectra of structural elements that build each zeolite framework. Based on the results of HF calculations, normal vibrations have been visualized and detailed analysis of pseudolattice range of resulting theoretical spectra have been carried out. Obtained results have been applied for interpretation of experimental spectra of selected zeolites. Copyright © 2018 Elsevier B.V. All rights reserved.

The growth of zeolites A, X and mordenite in space

NASA Technical Reports Server (NTRS)

Sacco, Albert, Jr.; Bac, N.; Coker, E. N.; Dixon, A. G.; Warzywoda, J.; Thompson, R. W.

1994-01-01

Zeolites are a class of crystalline aluminosilicate materials that form the backbone of the chemical process industry worldwide. They are used primarily as adsorbents and catalysts and support to a significant extent the positive balance of trade realized by the chemical industry in the United States (around $19 billion in 1991). The magnitude of their efforts can be appreciated when one realizes that since their introduction as 'cracking catalysts' in the early 1960's, they have saved the equivalent of 60 percent of the total oil production from Alaska's North Slope. Thus the performance of zeolite catalysts can have a profound effect on the U.S. economy. It is estimated that a 1 percent increase in yield of the gasoline fraction per barrel of oil would represent a savings of 22 million barrels of crude oil per year, representing a reduction of $400 million in the United States' balance of payments. Thus any activity that results in improvement in zeolite catalyst performance is of significant scientific and industrial interest. In addition, due to their 'stability,' uniformity, and, within limits, their 'engineerable' structures, zeolites are being tested as potential adsorbents to purify gases and liquids at the parts-per-billion levels needed in today's electronic, biomedical, and biotechnology industries and for the environment. Other exotic applications, such as host materials for quantum-confined semiconductor atomic arrays, are also being investigated. Because of the importance of this class of material, extensive efforts have been made to characterize their structures and to understand their nucleation and growth mechanisms, so as to be able to custom-make zeolites for a desired application. To date, both the nucleation mechanics and chemistry (such as what are the 'key' nutrients) are, as yet, still unknown for many, if not all, systems. The problem is compounded because there is usually a 'gel' phase present that is assumed to control the degree of supersaturation, and this gel undergoes a continuous 'polymerization' type reaction during nucleation and growth. Generally, for structure characterization and diffusion studies, which are useful in evaluating zeolites for improving yield in petroleum refining as well as for many of the proposed new applications (e.g., catalytic membranes, molecular electronics, chemical sensors) large zeolites (greater than 100 to 1000 times normal size) with minimum lattice defects are desired. Presently, the lack of understanding of zeolite nucleation and growth precludes the custom design of zeolites for these or other uses. It was hypothesized that the microgravity levels achieved in an orbiting spacecraft could help to isolate the possible effects of natural convection (which affects defect formation) and minimize sedimentation, which occurs since zeolites are twice as dense as the solution from which they are formed. This was expected to promote larger crystals by allowing growing crystals a longer residence time in a high-concentration nutrient field. Thus it was hypothesized that the microgravity environment of Earth orbit would allow the growth of large, more defect-free zeolite crystals in high yield.

Vitrification of copper flotation waste.

PubMed

Karamanov, Alexander; Aloisi, Mirko; Pelino, Mario

2007-02-09

The vitrification of an hazardous iron-rich waste (W), arising from slag flotation of copper production, was studied. Two glasses, containing 30wt% W were melted for 30min at 1400 degrees C. The first batch, labeled WSZ, was obtained by mixing W, blast furnace slag (S) and zeolite tuff (Z), whereas the second, labeled WG, was prepared by mixing W, glass cullet (G), sand and limestone. The glass frits showed high chemical durability, measured by the TCLP test. The crystallization of the glasses was evaluated by DTA. The crystal phases formed were identified by XRD resulting to be pyroxene and wollastonite solid solutions, magnetite and hematite. The morphology of the glass-ceramics was observed by optical and scanning electron microscopy. WSZ composition showed a high rate of bulk crystallization and resulted to be suitable for producing glass-ceramics by a short crystallization heat-treatment. WG composition showed a low crystallization rate and good sinterability; glass-ceramics were obtained by sinter-crystallization of the glass frit.

Facile preparation of hierarchically porous diatomite/MFI-type zeolite composites and their performance of benzene adsorption: the effects of NaOH etching pretreatment.

PubMed

Yu, Wenbin; Yuan, Peng; Liu, Dong; Deng, Liangliang; Yuan, Weiwei; Tao, Bo; Cheng, Hefa; Chen, Fanrong

2015-03-21

Hierarchically porous diatomite/MFI-type zeolite (Dt/Z) composites with excellent benzene adsorption performance were prepared. The hierarchical porosity was generated from the microporous zeolite coated at the surface of diatom frustules and from the macroporous diatomite support. A facile NaOH etching method was employed for the first time to treat the frustule support, followed by hydrothermal growth of MFI-type zeolite at the surface of frustules previously seeded with nanocrystalline silicalite-1 (Sil-1). NaOH etching enlarged the pores on diatom frustules and further increased the coated zeolite contents (W(z)). The central macropore size of the diatom frustules increased from approximately 200-500 nm to 400-1000 nm after NaOH etching. The W(z) could reach 61.2%, while the macroporosity of the composites was largely preserved due to more voids for zeolite coating being formed by NaOH etching. The Dt/Z composites exhibited higher benzene adsorption capacity per unit mass of zeolite and less mass transfer resistance than Sil-1, evaluated via a method of breakthrough curves. These results demonstrate that etching of a diatomite support is a facile but crucial process for the preparation of Dt/Z composites, enabling the resulting composites to become promising candidates for uses in volatile organic compounds emission control. Copyright © 2014 Elsevier B.V. All rights reserved.

The link between volcanism and plutonism in epizonal magma systems; high-precision U–Pb zircon geochronology from the Organ Mountains caldera and batholith, New Mexico

USGS Publications Warehouse

Rioux, Matthew; Farmer, Lang; Bowring, Samuel; Wooton, Kathleen M.; Amato, Jeffrey M.; Coleman, Drew S.; Verplanck, Philip L.

2016-01-01

The Organ Mountains caldera and batholith expose the volcanic and epizonal plutonic record of an Eocene caldera complex. The caldera and batholith are well exposed, and extensive previous mapping and geochemical analyses have suggested a clear link between the volcanic and plutonic sections, making this an ideal location to study magmatic processes associated with caldera volcanism. Here we present high-precision thermal ionization mass spectrometry U–Pb zircon dates from throughout the caldera and batholith, and use these dates to test and improve existing petrogenetic models. The new dates indicate that Eocene volcanic and plutonic rocks in the Organ Mountains formed from ~44 to 34 Ma. The three largest caldera-related tuff units yielded weighted mean 206Pb/238U dates of 36.441 ± 0.020 Ma (Cueva Tuff), 36.259 ± 0.016 Ma (Achenback Park tuff), and 36.215 ± 0.016 Ma (Squaw Mountain tuff). An alkali feldspar granite, which is chemically similar to the erupted tuffs, yielded a synchronous weighted mean 206Pb/238U date of 36.259 ± 0.021 Ma. Weighted mean 206Pb/238U dates from the larger volume syenitic phase of the underlying Organ Needle pluton range from 36.130 ± 0.031 to 36.071 ± 0.012 Ma, and the youngest sample is 144 ± 20 to 188 ± 20 ka younger than the Squaw Mountain and Achenback Park tuffs, respectively. Younger plutonism in the batholith continued through at least 34.051 ± 0.029 Ma. We propose that the Achenback Park tuff, Squaw Mountain tuff, alkali feldspar granite and Organ Needle pluton formed from a single, long-lived magma chamber/mush zone. Early silicic magmas generated by partial melting of the lower crust rose to form an epizonal magma chamber. Underplating of the resulting mush zone led to partial melting and generation of a high-silica alkali feldspar granite cap, which erupted to form the tuffs. The deeper parts of the chamber underwent continued recharge and crystallization for 144 ± 20 ka after the final eruption. Calculated magmatic fluxes for the Organ Needle pluton range from 0.0006 to 0.0030 km3/year, in agreement with estimates from other well-studied plutons. The petrogenetic evolution proposed here may be common to many small-volume silicic volcanic systems.

Eruption and emplacement of a laterally extensive, crystal-rich, and pumice-free ignimbrite (the Cretaceous Kusandong Tuff, Korea)

NASA Astrophysics Data System (ADS)

Sohn, Y. K.; Son, M.; Jeong, J. O.; Jeon, Y. M.

2009-10-01

The Cretaceous Kusandong Tuff, Korea, is a thin (1-5 m thick) but laterally extensive (~ 200 km) silicic ignimbrite emplaced in a fluviolacustrine basin adjacent to a continental volcanic arc. The tuff has been used as an excellent key bed because of its great lateral continuity and unique lithology, characterized by the virtual absence of juvenile clasts and an abundance of quartz and feldspar crystals (up to 55-73 vol.%). The tuff is mostly massive and ungraded and locally shows crude internal layering, basal inverse grading and near-top normal grading of crystals, either erosional or non-erosional lower surfaces, and flat-lying to imbricated grain fabrics. Fragile intraformational clasts of mudstone and tuff are also included. These features provide only ambiguous information on the properties of the responsible pyroclastic density currents: i.e. whether they were dense and laminar or dilute and turbulent. The overall lateral continuity and sheet-like geometry of the tuff suggests, however, that the transport system of the currents was highly expanded, dilute, and turbulent. A plug-flow or slab-flow model cannot explain the origin of crude internal layering, imbricated grain fabrics, and the high crystal content, which is most likely the result of vigorous sorting processes within a dilute and turbulent current. Features indicative of deposition from a dense and laminar transporting medium are locally present, suggesting that a dense and laminar depositional system could develop locally at the base of the dilute and turbulent transport system. The virtual absence of juvenile clasts in the tuff is interpreted to be due to rapid ascent, sudden decompression, and full fragmentation of silicic magma into fine glass shards and crystals. Scarcity of basement-derived accidental components together with the absence of pumiceous fallout deposits beneath the tuff is interpreted to be due to shallow-level fragmentation of magma followed by immediate generation of pyroclastic density currents from shallow-level blasts at the onset of eruption. The eruption occurred through multiple vent sites in a short period of time, producing a seemingly single but actually composite ignimbrite unit. Such an eruption was probably possible because of a regional tectonic event within the basin or in its vicinity. It is proposed that a composite ignimbrite with the characteristics of the Kusandong Tuff can be an exemplary product of syntectonic volcanism that can provide an insight into the interpretation of structural and stratigraphic evolution of a sedimentary basin.

Ash-flow tuffs of the Galiuro Volcanics in the northern Galiuro Mountains, Pinal County, Arizona

USGS Publications Warehouse

Krieger, Medora Louise Hooper

1979-01-01

The upper Oligocene and lower Miocene Galiuro Volcanics in the northern part of the Galiuro Mountains contains two distinctive major ash-flow tuff sheets, the Holy Joe and Aravaipa Members. These major ash-flows illustrate many features of ash-flow geology not generally exposed so completely. The Holy Joe Member, composed of a series of densely welded flows of quartz latite composition that make up a simple cooling unit. is a rare example of a cooling unit that has a vitrophyre at the top as well as at the base. The upper vitrophyre does not represent a cooling break. The Aravaipa Member. a rhyolite, is completely exposed in Aravaipa and other canyons and on Table Mountain. Remarkable exposures along Whitewash Canyon exhibit the complete change from a typical stacked-up interior zonation of an ash flow to a non welded distal margin. Vertical and horizontal changes in welding, crystallization, specific gravity, and lithology are exposed. The ash flow can be divided into six lithologic zones. The Holy Joe and Aravaipa Members of the Galiuro Volcanics are so well exposed and so clearly show characteristic features of ash-flow tuffs that they could be a valuable teaching aid and a source of theses for geology students.

Completion Report for Well ER-EC-5

DOE Office of Scientific and Technical Information (OSTI.GOV)

Bechtel Nevada

2004-10-01

Well ER-EC-5 was drilled for the U.S. Department of Energy, National Nuclear Security Administration Nevada Site Office in support of the Nevada Environmental Restoration Project at the Nevada Test Site, Nye County, Nevada. This well was drilled in the summer of 1999 as part of the U.S. Department of Energy's hydrogeologic investigation program in the Western Pahute Mesa - Oasis Valley region just west of the Nevada Test Site. A 44.5-centimeter surface hole was drilled and cased off to a depth of 342.6 meters below ground surface. The borehole diameter was then decreased to 31.1 centimeters for drilling to amore » total depth of 762.0 meters. One completion string with three isolated slotted intervals was installed in the well. A preliminary composite, static water level was measured at the depth of 309.9 meters, 40 days after installation of the completion string. Detailed lithologic descriptions with stratigraphic assignments are included in the report. These are based on composite drill cuttings collected every 3 meters, and 18 sidewall samples taken at various depths below 349.6 meters, supplemented by geophysical log data and results from detailed chemical and mineralogical analyses of rock samples. The well penetrated Tertiary-age tuffs of the Thirsty Canyon Group, caldera moat-filling sedimentary deposits, lava of the Beatty Wash Formation, and landslide breccia and tuffs of the Timber Mountain Group. The well reached total depth in welded ashflow tuff of the Ammonia Tanks Tuff after penetrating 440.1 meters of this unit, which is also the main water-producing unit in the well. The geologic interpretation of data from this well constrains the western margin of the Ammonia Tanks caldera to the west of the well location.« less

Geochemical and Petrological Studies of Peralkaline Rocks from Laborcita de San Javier, Chihuahua, Mexico

NASA Astrophysics Data System (ADS)

Lozano, J. E.; Espejel-Garcia, V. V.; Villalobos-Aragon, A.

2013-05-01

Peralkaline igneous rocks are characterized by a lower total aluminum content in comparison to the total alkalis content (Na + K), and are important to determine the tectonic environment in which they formed. The majority of the volcanic activity in Chihuahua State, northern Mexico, is mostly related to the formation of the Sierra Madre Occidental (SMO), product of the subduction of the Farallon plate. Volcanic activity of Paleogene age (late Oligocene) to the SW of Chihuahua city, specifically in the towns of Laborcita de San Javier and Cusihuiriachic, includes 27.5 M.a. peralkaline tuffs, capping the older rhyolites and andesites of the SMO. This sequence becomes thicker and more prominent towards the west. A volcanic section of more than 1,000 m thick is exposed in the Laborcita area, which ranges in age from 27 to 35 Ma. The oldest (bottom) unit is a calc-alkaline felsic ash-flow tuff and rhyolitic lavas interbedded with flows of mafic to intermediate composition. Overlying this unit, there is a basaltic andesite with an age of 30 to 33 Ma. Right at the top of this sequence, there is the widespread peralkaline ash-flow tuff (27.5 M.a.), focus of this study. Geochemical analyses performed to rhyolitic tuffs by Mauger and Dayvault (1983), have a peralkalinity index ranging from 0.94 to 1.20, while analyses prepared for this project only reach an index of 0.60. The appearance of peralkaline rocks in the Chihuahua State indicates the change of tectonic regime from compression (Farallon plate subduction) to distension (Basin and Range and/or Rio Grande Rift), about 27 M.a. ago.

Rare Earth coordination polymers with zeolite topology constructed from 4-connected building units.

PubMed

Guo, Xiaodan; Zhu, Guangshan; Li, Zhongyue; Chen, Yan; Li, Xiaotian; Qiu, Shilun

2006-05-15

A series of rare earth coordination polymers, M(BTC)(DMF)(DMSO) (M = Tb (1), Ho (2), Er (3), Yb (4), Y (5)), with zeolite ABW topology have been synthesized under mild conditions. They exhibit the same three-dimensional (3D) architecture and crystallize in monoclinic symmetry space group P2(1)/n. Their structures are built up from inorganic and organic 4-connected building units, whose vertex symbols are 4.4.6.6.6.8. The building units link to each other to generate approximate 5 x 8 angstroms2 channels along the [100] direction. The luminescent and magnetic properties of these compounds are investigated, and the results reveal that they could be anticipated to be potential antiferromagnetic and fluorescent materials.

Geohydrology of volcanic tuff penetrated by test well UE-25b#1, Yucca Mountain, Nye County, Nevada

USGS Publications Warehouse

Lahoud, R.G.; Lobmeyer, D.H.; Whitfield, M.S.

1984-01-01

Test well UE-25bNo1, located on the east side of Yucca Mountain in the southwestern part of the Nevada Test Site, was drilled to a total depth of 1,220 meters and hydraulically tested as part of a program to evaluate the suitability of Yucca Mountain as a nuclear-waste repository. The well penetrated almost 46 meters of alluvium and 1,174 meters of Tertiary volcanic tuffs. The composite hydraulic head for aquifers penetrated by the well was 728.9 meters above sea level (471.4 meters below land surface) with a slight decrease in loss of hydraulic head with depth. Average hydraulic conductivities for stratigraphic units determined from pumping tests, borehole-flow surveys, and packer-injection tests ranged from less than 0.001 meter per day for the Tram Member of the Crater Flat Tuff to 1.1 meters per day for the Bullfrog Member of the Crater Flat Tuff. The small values represented matrix permeability of unfractured rock; the large values probably resulted from fracture permeability. Chemical analyses indicated that the water is a soft sodium bicarbonate type, slightly alkaline, with large concentrations of dissolved silica and sulfate. Uncorrected carbon-14 age dates of the water were 14,100 and 13,400 years. (USGS)

Correlation of Pliocene and Pleistocene tephra layers between the Turkana Basin of East Africa and the Gulf of Aden

USGS Publications Warehouse

Brown, F.H.; Sarna-Wojcicki, A. M.; Meyer, C.E.; Haileab, B.

1992-01-01

Electron-microprobe analyses of glass shards from volcanic ash in Pliocene and Pleistocene deep-sea sediments in the Gulf of Aden and the Somali Basin demonstrate that most of the tephra layers correlate with tephra layers known on land in the Turkana Basin of northern Kenya and southern Ethiopia. Previous correlations are reviewed, and new correlations proposed. Together these data provide correlations between the deep-sea cores, and to the land-based sections at eight levels ranging in age from about 4 to 0.7 Ma. Specifically, we correlate the Moiti Tuff (???4.1 Ma) with a tephra layer at 188.6 m depth in DSDP hole 231 and with a tephra layer at 150 m depth in DSDP hole 241, the Wargolo Tuff with a tephra layer at 179.7 m in DSDP Hole 231 and with a tephra layer at 155.3 m depth in DSDP Hole 232, the Lomogol Tuff (defined here) with a tephra layer at 165 m in DSDP Hole 232A, the Lokochot Tuff with a tephra layer at 140.1 m depth in DSDP Hole 232, the Tulu Bor Tuff with a tephra layer at 160.8 m depth in DSDP Hole 231, the Kokiselei Tuff with a tephra layer at 120 m depth in DSDP Hole 231 and with a tephra layer at 90.3 m depth in DSDP Hole 232, the Silbo Tuff (0.74 Ma) with a tephra layer at 35.5 m depth in DSDP Hole 231 and possibly with a tephra layer at 10.9 m depth in DSDP Hole 241. We also present analyses of other tephra from the deep sea cores for which correlative units on land are not yet known. The correlated tephra layers provide eight chronostratigraphic horizons that make it possible to temporally correlate paleoecological and paleoclimatic data between the terrestrial and deep-sea sites. Such correlations may make it possible to interpret faunal evolution in the Lake Turkana basin and other sites in East Africa within a broader regional or global paleoclimatic context. ?? 1992.

Volcanism at 1.45 Ma within the Yellowstone Volcanic Field, United States

NASA Astrophysics Data System (ADS)

Rivera, Tiffany A.; Furlong, Ryan; Vincent, Jaime; Gardiner, Stephanie; Jicha, Brian R.; Schmitz, Mark D.; Lippert, Peter C.

2018-05-01

Rhyolitic volcanism in the Yellowstone Volcanic Field has spanned over two million years and consisted of both explosive caldera-forming eruptions and smaller effusive flows and domes. Effusive eruptions have been documented preceding and following caldera-forming eruptions, however the temporal and petrogenetic relationships of these magmas to the caldera-forming eruptions are relatively unknown. Here we present new 40Ar/39Ar dates for four small-volume eruptions located on the western rim of the second-cycle caldera, the source of the 1.300 ± 0.001 Ma Mesa Falls Tuff. We supplement our new eruption ages with whole rock major and trace element chemistry, Pb isotopic ratios of feldspar, and paleomagnetic and rock magnetic analyses. Eruption ages for the effusive Green Canyon Flow (1.299 ± 0.002 Ma) and Moonshine Mountain Dome (1.302 ± 0.003 Ma) are in close temporal proximity to the eruption age of the Mesa Falls Tuff. In contrast, our results indicate a period of volcanism at ca 1.45 Ma within the Yellowstone Volcanic Field, including the eruption of the Bishop Mountain Flow (1.458 ± 0.002 Ma) and Tuff of Lyle Spring (1.450 ± 0.003 Ma). These high-silica rhyolites are chemically and isotopically distinct from the Mesa Falls Tuff and related 1.3 Ma effusive eruptions. The 40Ar/39Ar data from the Tuff of Lyle Spring demonstrate significant antecrystic inheritance, prevalent within the upper welded ash-flow tuff matrix, and minimal within individual pumice. Antecrysts are up to 20 kyr older than the eruption, with subpopulations of grains occurring every few thousand years. We interpret these results as an indicator for the timing of magmatic pulses into a growing magmatic system that would ultimately erupt the Tuff of Lyle Spring, and which we more broadly interpret as the tempo of crustal accumulation associated with bimodal magmatism. We propose a system whereby chemically, isotopically, and temporally distinct, isolated small-volume magma batches are periodically generated and erupted in a low magmatic flux state, which is punctuated by larger volume caldera-forming eruptions.

Specific surface area of a crushed welded tuff before and after aqueous dissolution

USGS Publications Warehouse

Reddy, M.M.; Claassen, H.C.

1994-01-01

Specific surface areas were measured for several reference minerals (anorthoclase, labradorite and augite), welded tuff and stream sediments from Snowshoe Mountain, near Creede, Colorado. Crushed and sieved tuff had an unexpectedly small variation in specific surface area over a range of size fractions. Replicate surface area measurements of the largest and smallest tuff particle size fractions examined (1-0.3 mm and <0.212 mm) were 2.3 ?? 0.2 m2/g for each size fraction. Reference minerals prepared in the same way as the tuff had smaller specific surface areas than that of the tuff of the same size fraction. Higher than expected tuff specific surface areas appear to be due to porous matrix. Tuff, reacted in solutions with pH values from 2 to 6, had little change in specific surface area in comparison with unreacted tuff. Tuff, reacted with solutions having high acid concentrations (0.1 M hydrochloric acid or sulfuric-hydrofluoric acid), exhibited a marked increase in specific surface area compared to unreacted tuff. ?? 1994.

Recommended nomenclature for zeolite minerals: report of the subcommittee on zeolites of the International Mineralogical Association, Commission of New Minerals and Mineral Names

USGS Publications Warehouse

Coombs, D.S.; Alberti, A.; Armbruster, T.; Artioli, G.; Colella, C.; Galli, E.; Grice, Joel D.; Liebau, F.; Mandarino, J.A.; Minato, H.; Nickel, E.H.; Passaglia, E.; Peacor, D.R.; Quartieri, S.; Rinaldi, R.; Ross, M.; Sheppard, R.A.; Tillmanns, E.; Vezzalini, G.

1998-01-01

This report embodies recommendations on zeolite nomenclature approved by the International Mineralogical Association Commission of New Minerals and Mineral Names. In a working definition of a zeolite mineral used for review, interrupted tetrahedral framework structures are accepted where other zeolitic properties prevail, and complete substitution by elements other than Si and Al is allowed. Separate species are recognized in topologically distinctive compositional series in which different extra-framework cations are the most abundance in atomic proportions. To name these, the appropriate chemical symbol is attached by a hyphen to the series name as a suffix except for the names harmotome, pollucite and wairakite in the phillipsite and analcime series. Differences in space-group symmetry and in order-disorder relationships in zeolites having the same topologically distinctive framework do not in general provide adequate grounds for recognition of separate species. Zeolite species are not to be distinguished solely on Si:Al ratio except for heulandite (Si:Al < 4.0) and clinoptilolite (Si:Al ??? 4.0). Dehydration, partial hydration, and over-hydration are not sufficient grounds for the recognition of separate species of zeolites. Use of the term 'ideal formula' should be avoided in referring to a simplified or averaged formula of a zeolite. Newly recognized species in compositional series are as follows: brewsterite-Sr.-Ba: chabazite-Ca.-Na.-K; clinoptilolite-K, -Na, -Ca: dachiardite-Ca, -Na; erionite-K, -Ca: faujasite-Na, -Ca, -Na: paulingite-K. -Ca; phillipsite-Na, -Ca, -Ka; stilbite-Ca, -Na. Key references, type locality, origin of name, chemical data. IZA structure-type symbols, space-group symmetry; unit-cell dimensions, and comments on structure are listed for 13 compositional series, 82 accepted zeolite mineral species, and three of doubtful status. Herschelite, leonhardite, svetlozarite, and wellsite are discredited as mineral species names. Obsolete and discredited names are listed.

Miocene calc-alkaline magmatism, calderas, and crustal extension in the Kofa and Castle Dome Mountains, southwestern Arizona

DOE Office of Scientific and Technical Information (OSTI.GOV)

Grubensky, M.J.; Bagby, W.C.

1990-11-10

Two widespread lower Miocene rhyolite ash flow tuffs in the Kofa and Castle Dome Mountains of southwestern Arizona are products of caldera-forming eruptions. These closely erupted tuffs, the tuff of Yaqui Tanks and the tuff of Ten Ewe Mountain, are approximately 22 Ma in age and their eruptions culminate a 1- to 2-m.y.-long burst of calc-alkaline volcanic activity centered on the northern Castle Dome Mountains. Exotic blocks of Proterozoic and Mesozoic crystalline rocks up to 20 m across are present in exposures of the tuff of Yaqui Tanks exposed in the central Castle Dome Mountains and the southern Kofa Mountains.more » A single, thick cooling unit of the tuff of Ten Ewe Mountain that includes thick lenses of mesobreccia marks the location of the younger caldera that extends from Palm Canyon in the western Kofa Mountains eastward more than 7 km along strike to the central part of the range. Large residual Bouguer gravity anomalies, one beneath each inferred caldera, are interpreted as batholithic rocks or low-density caldera fill. Caldera-related volcanism in the Kofa region occurred during a transition in extensional tectonic regimes: From a regime of east-west trending uplifts and basins to a regime manifest primarily by northwest striking normal faults. A narrow corridor of folding and strike-slip faulting formed during volcanism in the southern Kofa Mountains. Upper Oligocene or lower Miocene coarse sedimentary rocks along the southern flank of the Chocolate Mountains anticlinorium in the southern Castle Dome Mountains mark the periphery of a basin similar to other early and middle Tertiary basins exposed in southern California. The volcanic section of the Kofa region was dissected by high-angle normal faults related to northeast-southwest oriented crustal extension typical of the southern Basin and Range province.« less

Volcanic Stratigraphy of the Quaternary Rhyolite Plateau in Yellowstone National Park

USGS Publications Warehouse

Christiansen, Robert L.; Blank, H. Richard

1972-01-01

The volcanic sequence of the Quaternary Yellowstone plateau consists of rhyolites and basalts representing three volcanic cycles. The major events of each cycle were eruption of a voluminous ash-flow sheet and formation of a large collapse caldera. Lesser events of each cycle were eruption of precaldera and postcaldera rhyolitic lava flows and marginal basaltic lavas. The three major ash-flow sheets are named and designated in this report as formations within the Yellowstone Group. The lavas are assigned to newly named formations organized around the three ash-flow sheets of the Yellowstone Group to represent the volcanic cycles. Rocks of the first volcanic cycle comprise the precaldera Junction Butte Basalt and rhyolite of Broad Creek; the Huckleberry Ridge Tuff of the Yellowstone Group; and the postcaldera Lewis Canyon Rhyolite and basalt of The Narrows. Rocks of the second volcanic cycle do not crop out within Yellowstone National Park, and only the major unit, the Mesa Falls Tuff of the Yellowstone Group, is named here. The third volcanic cycle is represented by the precaldera Mount Jackson Rhyolite and Undine Falls Basalt; the Lava Creek Tuff of the Yellowstone Group; and the postcaldera Plateau Rhyolite and five post-Lava Creek basaltic sequences. Collapse to form the compound and resurgent Yellowstone caldera was related to eruption of the Lava Creek Tuff. The Plateau Rhyolite is divided into six members - the Mallard Lake, Upper Basin, Obsidian Creek, Central Plateau, Shoshone Lake Tuff, and Roaring Mountain Members; all but the Mallard Lake postdate resurgent doming of the caldera. The basalts are divided into the Swan Lake Flat Basalt, Falls River Basalt, basalt of Mariposa Lake, Madison River Basalt, and Osprey Basalt. Sediments are intercalated in the volcanic section below the Huckleberry Ridge and Mesa Falls Tuffs and within the Junction Butte Basalt, sediments and basalts of The Narrows, Undine Falls Basalt, Plateau Rhyolite, and Osprey Basalt.

Neogene Fallout Tuffs from the Yellowstone Hotspot in the Columbia Plateau Region, Oregon, Washington and Idaho, USA

PubMed Central

Nash, Barbara P.; Perkins, Michael E.

2012-01-01

Sedimentary sequences in the Columbia Plateau region of the Pacific Northwest ranging in age from 16–4 Ma contain fallout tuffs whose origins lie in volcanic centers of the Yellowstone hotspot in northwestern Nevada, eastern Oregon and the Snake River Plain in Idaho. Silicic volcanism began in the region contemporaneously with early eruptions of the Columbia River Basalt Group (CRBG), and the abundance of widespread fallout tuffs provides the opportunity to establish a tephrostratigrahic framework for the region. Sedimentary basins with volcaniclastic deposits also contain diverse assemblages of fauna and flora that were preserved during the Mid-Miocene Climatic Optimum, including Sucker Creek, Mascall, Latah, Virgin Valley and Trout Creek. Correlation of ashfall units establish that the lower Bully Creek Formation in eastern Oregon is contemporaneous with the Virgin Valley Formation, the Sucker Creek Formation, Oregon and Idaho, Trout Creek Formation, Oregon, and the Latah Formation in the Clearwater Embayment in Washington and Idaho. In addition, it can be established that the Trout Creek flora are younger than the Mascall and Latah flora. A tentative correlation of a fallout tuff from the Clarkia fossil beds, Idaho, with a pumice bed in the Bully Creek Formation places the remarkably well preserved Clarkia flora assemblage between the Mascall and Trout Creek flora. Large-volume supereruptions that originated between 11.8 and 10.1 Ma from the Bruneau-Jarbidge and Twin Falls volcanic centers of the Yellowstone hotspot in the central Snake River Plain deposited voluminous fallout tuffs in the Ellensberg Formation which forms sedimentary interbeds in the CRBG. These occurrences extend the known distribution of these fallout tuffs 500 km to the northwest of their source in the Snake River Plain. Heretofore, the distal products of these large eruptions had only been recognized to the east of their sources in the High Plains of Nebraska and Kansas. PMID:23071494

Neogene fallout tuffs from the Yellowstone hotspot in the Columbia Plateau region, Oregon, Washington and Idaho, USA.

PubMed

Nash, Barbara P; Perkins, Michael E

2012-01-01

Sedimentary sequences in the Columbia Plateau region of the Pacific Northwest ranging in age from 16-4 Ma contain fallout tuffs whose origins lie in volcanic centers of the Yellowstone hotspot in northwestern Nevada, eastern Oregon and the Snake River Plain in Idaho. Silicic volcanism began in the region contemporaneously with early eruptions of the Columbia River Basalt Group (CRBG), and the abundance of widespread fallout tuffs provides the opportunity to establish a tephrostratigrahic framework for the region. Sedimentary basins with volcaniclastic deposits also contain diverse assemblages of fauna and flora that were preserved during the Mid-Miocene Climatic Optimum, including Sucker Creek, Mascall, Latah, Virgin Valley and Trout Creek. Correlation of ashfall units establish that the lower Bully Creek Formation in eastern Oregon is contemporaneous with the Virgin Valley Formation, the Sucker Creek Formation, Oregon and Idaho, Trout Creek Formation, Oregon, and the Latah Formation in the Clearwater Embayment in Washington and Idaho. In addition, it can be established that the Trout Creek flora are younger than the Mascall and Latah flora. A tentative correlation of a fallout tuff from the Clarkia fossil beds, Idaho, with a pumice bed in the Bully Creek Formation places the remarkably well preserved Clarkia flora assemblage between the Mascall and Trout Creek flora. Large-volume supereruptions that originated between 11.8 and 10.1 Ma from the Bruneau-Jarbidge and Twin Falls volcanic centers of the Yellowstone hotspot in the central Snake River Plain deposited voluminous fallout tuffs in the Ellensberg Formation which forms sedimentary interbeds in the CRBG. These occurrences extend the known distribution of these fallout tuffs 500 km to the northwest of their source in the Snake River Plain. Heretofore, the distal products of these large eruptions had only been recognized to the east of their sources in the High Plains of Nebraska and Kansas.

Post-middle Miocene Tuffs of Bodie Hills and Mono Basin, California: Paleomagnetic Reference Directions and Vertical Axis Rotation

NASA Astrophysics Data System (ADS)

Lindeman, J. R.; Pluhar, C. J.; Farner, M. J.

2013-12-01

The relative motions of the Pacific and North American plates about the Sierra Nevada-North American Euler pole is accommodated by dextral slip along the San Andreas Fault System (~75%) and the Walker Lane-Eastern California Shear Zone system of faults, east of the Sierra Nevada microplate (~25%). The Bodie Hills and Mono Basin regions lie within the Walker Lane and partially accommodate deformation by vertical axis rotation of up to 60o rotation since ~9.4 Ma. This region experienced recurrent eruptive events from mid to late Miocene, including John et al.'s (2012) ~12.05 Ma Tuff of Jack Springs (TJS) and Gilbert's (1968) 11.1 - 11.9 Ma 'latite ignimbrite' east of Mono Lake. Both tuffs can be identified by phenocrysts of sanidine and biotite in hand specimens, with TJS composed of a light-grey matrix and the latite ignimbrite composed of a grey-black matrix. Our paleomagnetic results show these units to both be normal polarity, with the latite ignimbrite exhibiting a shallow inclination. TJS's normal polarity is consistent with emplacement during subchron C5 An. 1n (12.014 - 12.116 Ma). The X-ray fluorescence analyses of fiamme from TJS in Bodie Hills and the latite ignimbrite located east of Mono Lake reveal them both to be rhyolites with the latite ignimbrite sharing elevated K composition seen in the slightly younger Stanislaus Group (9.0 - 10.2 Ma). We establish a paleomagnetic reference direction of D = 352.8o I = 42.7o α95 = 7.7o n = 5 sites (42 samples) for TJS in the Bodie Hills in a region hypothesized by Carlson (2012) to have experienced low rotation. Our reference for Gilbert's latite ignimbrite (at Cowtrack Mountain) is D = 352.9o I = 32.1o α95 = 4.7o. This reference locality is found on basement highland likely to have experienced less deformation then the nearby Mono Basin since ignimbrite emplacement. Paleomagnetic results from this latite ignimbrite suggests ~98.2o × 5.5o of clockwise vertical axis rotation of parts of eastern Mono Basin since unit emplacement. A welded 11.7 Ma (K-Ar; Drake, 1979) rhyolitic tuff near Trafton Mountain appears similar in composition to TJS. Drake's tuff exhibits a reversed polarity, consistent with reversed polarity subchron C5r.3r (11.614 - 12.014 Ma) and distinguishes this tuff from TJS and Gilbert's latite ignimbrite.

Recognition of primary and diagenetic magnetizations to determine the magnetic polarity record and timing of deposition of the moat-fill rocks of the Oligocene Creede Caldera, Colorado

USGS Publications Warehouse

Reynolds, Richard L.; Rosenbaum, Joseph G.; Sweetkind, Donald S.; Lanphere, Marvin A.; Robert, Andrew P.; Verosub, Kenneth L.

2000-01-01

Sedimentary and volcaniclastic rocks of the Oligocene Creede Formation fill the moat of the Creede caldera, which formed at about 26.9 Ma during the eruption of the Snowshoe Mountain Tuff. Paleomagnetic and rock magnetic studies of two cores (418 and 703 m long) that penetrated the lower half of the Creede Formation, in addition to paleomagnetic and isotopic dating studies of stratigraphically bracketing volcanic units, provide information on the age and the time span of sedimentation of the caldera fill. Normal polarity magnetization are found in Snowshoe Mountain Tuff beneath the moat sediments; in detrital-magnetite-bearing graded tuffs near the bottom of the moat fill; in an ash-fall deposit about 200 m stratigraphically about the top of core 2; and in postcaldera lava flows of the Fisher Dacite that overlie the Creede Formation. Normal polarity also characterizes detrital-magnetite-bearing tuff and sandstone unites within the caldera moat rocks that did not undergo severe sulfidic alteration. The combination of initially low magnitude of remanent magnetization and the destructive effects of subsequent diagenetic sulfidization on detrital iron oxides results in a poor paleomagnetic record for the fine-grained sedimentary rocks of the Creede Formation. these fine-grained rocks have either normal or revered polarity magnetizations that are carried by magnetite and/or maghemite. Many more apparent reversals are found that can be accommodated by any geomagnetic polarity time scale over the interval spanned by the ages of the bracketing extrusive rocks. Moreover, opposite polarity magnetization are found in specimens separated by only a few centimeters, without intervening hiatuses, and by specimens in several tuff beds, each of which represents a single depositional event. These polarity changes cannot, therefore, be attributed to detrital remanent magnetization. Many polarity changes are apparently related to chemical remanent magnetizations carried by postdepositional magnetite and maghemite that formed in rocks in which most or all detrital megnetic iron oxide was destroyed. Incipient oxidation of early diagenetic pyrite may have normal polarity Snowshoe Mountain Tuff (26.89 ± 0.0 Ma, 1 δ) and on the normal polarity postcaldera Fisher lava flows (as young as 26.23 ± 0.05 Ma, 1 δ) indicate that deposition of the Creede Formation spanned about 340-660 k.y. The intermittently defined normal polarity magnetization for the caldera-fill sequence, compared with different versions of the geomagnetic polarity time scale, is consistent with the shorter time span.

Anammox-zeolite system acting as buffer to achieve stable effluent nitrogen values.

PubMed

Yapsakli, Kozet; Aktan, Cigdem Kalkan; Mertoglu, Bulent

2017-02-01

For a successful nitrogen removal, Anammox process needs to be established in line with a stable partial nitritation pretreatment unit since wastewater influent is mostly unsuitable for direct treatment by Anammox. Partial nitritation is, however, a critical bottleneck for the nitrogen removal since it is often difficult to maintain the right proportions of NO 2 -N and NH 4 -N during long periods of time for Anammox process. This study investigated the potential of Anammox-zeolite biofilter to buffer inequalities in nitrite and ammonium nitrogen in the influent feed. Anammox-zeolite biofilter combines the ion-exchange property of zeolite with the biological removal by Anammox process. Continuous-flow biofilter was operated for 570 days to test the response of Anammox-zeolite system for irregular ammonium and nitrite nitrogen entries. The reactor demonstrated stable and high nitrogen removal efficiencies (approximately 95 %) even when the influent NO 2 -N to NH 4 -N ratios were far from the stoichiometric ratio for Anammox reaction (i.e. NO 2 -N to NH 4 -N ranging from 0 to infinity). This is achieved by the sorption of surplus NH 4 -N by zeolite particles in case ammonium rich influent came in excess with respect to Anammox stoichiometry. Similarly, when ammonium-poor influent is fed to the reactor, ammonium desorption took place due to shifts in ion-exchange equilibrium and deficient amount were supplied by previously sorbed NH 4 -N. Here, zeolite acted as a preserving reservoir of ammonium where both sorption and desorption took place when needed and this caused the Anammox-zeolite system to act as a buffer system to generate a stable effluent.

Voluminous lava-like precursor to a major ash-flow tuff: Low-column pyroclastic eruption of the Pagosa Peak Dacite, San Juan volcanic field, Colorado

USGS Publications Warehouse

Bachmann, Olivier; Dungan, M.A.; Lipman, P.W.

2000-01-01

The Pagosa Peak Dacite is an unusual pyroclastic deposit that immediately predated eruption of the enormous Fish Canyon Tuff (~5000 km3) from the La Garita caldera at 28 Ma. The Pagosa Peak Dacite is thick (to 1 km), voluminous (>200 km3), and has a high aspect ratio (1:50) similar to those of silicic lava flows. It contains a high proportion (40-60%) of juvenile clasts (to 3-4 m) emplaced as viscous magma that was less vesiculated than typical pumice. Accidental lithic fragments are absent above the basal 5-10% of the unit. Thick densely welded proximal deposits flowed rheomorphically due to gravitational spreading, despite the very high viscosity of the crystal-rich magma, resulting in a macroscopic appearance similar to flow-layered silicic lava. Although it is a separate depositional unit, the Pagosa Peak Dacite is indistinguishable from the overlying Fish Canyon Tuff in bulk-rock chemistry, phenocryst compositions, and 40Ar/39Ar age. The unusual characteristics of this deposit are interpreted as consequences of eruption by low-column pyroclastic fountaining and lateral transport as dense, poorly inflated pyroclastic flows. The inferred eruptive style may be in part related to synchronous disruption of the southern margin of the Fish Canyon magma chamber by block faulting. The Pagosa Peak eruptive sources are apparently buried in the southern La Garita caldera, where northerly extensions of observed syneruptive faults served as fissure vents. Cumulative vent cross-sections were large, leading to relatively low emission velocities for a given discharge rate. Many successive pyroclastic flows accumulated sufficiently rapidly to weld densely as a cooling unit up to 1000 m thick and to retain heat adequately to permit rheomorphic flow. Explosive potential of the magma may have been reduced by degassing during ascent through fissure conduits, leading to fracture-dominated magma fragmentation at low vesicularity. Subsequent collapse of the 75 x 35 km2 La Garita caldera and eruption of the Fish Canyon Tuff were probably triggered by destabilization of the chamber roof as magma was withdrawn during the Pagosa Peak eruption. (C) 2000 Elsevier Science B.V. All rights reserved.

Show Me the Mush! - Constraints From Voluminous Rhyolitic Ignimbrites of Bimodal and Calc-alkaline Settings on the Applicability of a Mush Model

NASA Astrophysics Data System (ADS)

Streck, M. J.

2012-12-01

Mush models have been popular in explaining crystal-poor rhyolites of a variety of settings. The classical mush model requires an abundance of very crystal-rich (>50%), intermediate (dacitic) magmas that upon compaction expel their interstitial liquids that erupt to give rise to rhyolitic lava flows and ignimbrites. In volcanic systems, a critical part in evaluating a mush model rests on providing evidence for the existence of suitable crystal-rich intermediate magmas that are consistent with the petrology of the erupted rhyolites. In my evaluation, I focus on providing constraints of whether or not suitable crystal mushes are likely to have existed and were instrumental in the production of a select series of voluminous (>100 km3) rhyolitic ignimbrites. Furthermore, the volcanic framework of each selected ignimbrite is used for assessing questions of "eruptibility" of magma types. The three main evaluated units representing 'hot-dry-reduced' rhyolites of bimodal settings are the 16-15.4 Ma Dinner Creek Tuff, the 9.7 Ma Devine Canyon Tuff, and 7.1 Ma Rattlesnake Tuff. All three tuffs erupted in eastern Oregon within a basalt-rhyolite suite. The key feature that makes them particularly valuable for this discussion is that each of the tuffs erupted a co-magmatic component that tracks the intermediate to mafic underpinnings to the rhyolitic magma. This allows a direct assessment of what intermediate magmas residing in close spatial proximity to the rhyolites looked like. On the other hand, other characteristics such as degree of chemical zoning, element trends, single or multiple cooling units, etc., vary considerably among the three tuffs thus covering a wide spectrum of rhyolites from bimodal settings. As representative of 'cool-wet-oxidized' rhyolites, I test applicability of the mush model on the tuffs and associated lavas of the Oligocene San Luis caldera system. This system represents strongly confocal and voluminous eruptions that are closely spaced in time at the end of the activity period of the Central Caldera Cluster of the Oligocene San Juan volcanic field, Colorado. Compositional intermediate underpinnings of each of the 'hot-dry-reduced' rhyolites fail geochemical requirements to represent suitable intermediate magmas. In addition, these underpinnings are crystal-poor and this is inconsistent with the required high crystallinity of magma mushes. Remelting scenarios to reduce crystallinities in intermediate magmas are excluded - again on geochemical grounds. Other complications with a model of voluminous crystal mushes beneath such rhyolites are the production of strong trace-element chemical gradation within single magma batches as well as multi-cyclic eruptions of crystal-poor rhyolites from the same system. For the system of 'cold-wet-oxidized' rhyolites, one of the challenges for a mush model is that interstitial melts of crystal-rich intermediate magmas compositionally deviate from erupted rhyolites when abundant amphibole (±sphene) is present, yet both phases are commonly expected phenocrystic phases at crystallinities when extraction of rhyolite from mush can take place.

Biochar, Bentonite and Zeolite Supplemented Feeding of Layer Chickens Alters Intestinal Microbiota and Reduces Campylobacter Load

PubMed Central

Prasai, Tanka P.; Walsh, Kerry B.; Bhattarai, Surya P.; Midmore, David J.; Van, Thi T. H.; Moore, Robert J.; Stanley, Dragana

2016-01-01

A range of feed supplements, including antibiotics, have been commonly used in poultry production to improve health and productivity. Alternative methods are needed to suppress pathogen loads and maintain productivity. As an alternative to antibiotics use, we investigated the ability of biochar, bentonite and zeolite as separate 4% feed additives, to selectively remove pathogens without reducing microbial richness and diversity in the gut. Neither biochar, bentonite nor zeolite made any significant alterations to the overall richness and diversity of intestinal bacterial community. However, reduction of some bacterial species, including some potential pathogens was detected. The microbiota of bentonite fed animals were lacking all members of the order Campylobacterales. Specifically, the following operational taxonomic units (OTUs) were absent: an OTU 100% identical to Campylobacter jejuni; an OTU 99% identical to Helicobacter pullorum; multiple Gallibacterium anatis (>97%) related OTUs; Bacteroides dorei (99%) and Clostridium aldenense (95%) related OTUs. Biochar and zeolite treatments had similar but milder effects compared to bentonite. Zeolite amended feed was also associated with significant reduction in the phylum Proteobacteria. All three additives showed potential for the control of major poultry zoonotic pathogens. PMID:27116607

CR-100 synthetic zeolite adsorption characteristics toward Northern Banat groundwater ammonia.

PubMed

Tomić, Željko; Kukučka, Miroslav; Stojanović, Nikoleta Kukučka; Kukučka, Andrej; Jokić, Aleksandar

2016-10-14

The adsorption characteristics of synthetic zeolite CR-100 in a fixed-bed system using continuous flow of groundwater containing elevated ammonia concentration were examined. The possibilities for adsorbent mass calculation throughout mass transfer zone using novel mathematical approach as well as zeolite adsorption capacity at every sampling point in time or effluent volume were determined. The investigated adsorption process consisted of three clearly separated steps indicated to sorption kinetics. The first step was characterized by decrease and small changes in effluent ammonia concentration vs. experiment time and quantity of adsorbed ammonia per mass unit of zeolite. The consequences of this phenomenon were showed in the plots of the Freundlich and the Langmuir isotherm models through a better linear correlation according as graphical points contingent to the first step were not accounted. The Temkin and the Dubinin-Radushkevich isotherm models showed the opposite tendency with better fitting for overall measurements. According to the obtained isotherms parameter data, the investigated process was found to be multilayer physicochemical adsorption, and also that synthetic zeolite CR-100 is a promising material for removal of ammonia from Northern Banat groundwater with an ammonia removal efficiency of 90%.

Enrichment process of biogas using simultaneous Absorption - Adsorption methods

NASA Astrophysics Data System (ADS)

Kusrini, Eny; Lukita, Maya; Gozan, Misri; Susanto, Bambang Heru; Nasution, Dedy Alharis; Rahman, Arif; Gunawan, Cindy

2017-03-01

Removal of CO2 in biogas is an essential methods to the purification and upgrading of biogas. Natural Clinoptilolite zeolites were evaluated as sorbents for purification of biogas that produced from palm oil mill effluent (POME) by anerobic-digestion method. The absorption and adsorption experiments were conducted in a fixed-bed two column adsorption unit by simultaneous absorption-adsorption method. The Ca(OH)2 solution with concentration of 0.062 M was used as absorption method. Sorbent for removal of CO2 in biogas have been prepared by modifying of Clinoptilolite zeolites with an acid (HCl, 2M) and alkaline (NaOH, 2M), calcined at 450°C and then coated using chitosan (0.5 w/v%) in order to increase their adsorption capacity. The removal of CO2 in biogas was achieved about ˜83% using 2.5 g of sorbent zeolite (2M)/chitosan dosage for each column, breakthrough time of 30 min, and flow rate of 100 mL/min. Clinoptilolite zeolites with modifications of an acid-alkaline and chitosan (zeolite (2M)/chitosan) are promising sorbents due to the amine groups from chitosan and high surface-volume ratio are one of important factors in a simultaneous absorption-adsorption method.

Distinguishing and correlating deposits from large ignimbrite eruptions using paleomagnetism: The Cougar Point Tuffs (mid-Miocene), southern Snake River Plain, Idaho, USA

NASA Astrophysics Data System (ADS)

Finn, David R.; Coe, Robert S.; Brown, Ethan; Branney, Michael; Reichow, Marc; Knott, Thomas; Storey, Michael; Bonnichsen, Bill

2016-09-01

In this paper, we present paleomagnetic, geochemical, mineralogical, and geochronologic evidence for correlation of the mid-Miocene Cougar Point Tuff (CPT) in southwest Snake River Plain (SRP) of Idaho. The new stratigraphy presented here significantly reduces the frequency and increases the scale of known SRP ignimbrite eruptions. The CPT section exposed at the Black Rock Escarpment along the Bruneau River has been correlated eastward to the Brown's Bench escarpment (six common eruption units) and Cassia Mountains (three common eruption units) regions of southern Idaho. The CPT records an unusual pattern of geomagnetic field directions that provides the basis for robust stratigraphic correlations. Paleomagnetic characterization of eruption units based on geomagnetic field variation has a resolution on the order of a few centuries, providing a strong test of whether two deposits could have been emplaced from the same eruption or from temporally separate events. To obtain reliable paleomagnetic directions, the anisotropy of anhysteretic remanence was measured to correct for magnetic anisotropy, and an efficient new method was used to remove gyroremanence acquired during alternating field demagnetization.

Background studies in support of a feasibility assessment on the use of copper-base materials for nuclear waste packages in a repository in tuff

DOE Office of Scientific and Technical Information (OSTI.GOV)

Van Konynenburg, R.A.; Kundig, K.J.A.; Lyman, W.S.

1990-06-01

This report combines six work units performed in FY`85--86 by the Copper Development Association and the International Copper Research Association under contract with the University of California. The work includes literature surveys and state-of-the-art summaries on several considerations influencing the feasibility of the use of copper-base materials for fabricating high-level nuclear waste packages for the proposed repository in tuff rock at Yucca Mountain, Nevada. The general conclusion from this work was that copper-base materials are viable candidates for inclusion in the materials selection process for this application. 55 refs., 48 figs., 22 tabs.

Zeolites on Mars: Possible environmental indicators in soils and sediments

NASA Technical Reports Server (NTRS)

Ming, D. W.; Gooding, J. L.

1988-01-01

Weathering products should serve as indicators of weathering environments and may provide the best evidence of the nature of climate change on Mars. No direct mineralogical measurements of Martian regolith were performed by the Viking missions, but the biology and X-ray fluorescence experiments provided some information on the physiochemical properties of Martian regolith. Most post-Viking studies of candidate weathering products have emphasized phyllosilicates and Fe-oxides; zeolites are potentially important, but overlooked, candidate Martian minerals. Zeolites would be important on Mars for three different reasons. First, they are major sinks of atmospheric gases and, per unit mass, are stronger and more efficient sorbents than are phyllosilicates. Secondly, they can be virtually unique sorbents and shelters for organic compounds and possible catalysts for organic-based reactions. Finally, their exchangeable ions are good indicators of the chemical properties of solutions with which they have communicated. Accordingly, the search for information on past compositions of the Martian atmosphere and hydrosphere should find zeolites to be rich repositories.

Identification of mineral composition and weathering product of tuff using reflectance spectroscopy

NASA Astrophysics Data System (ADS)

Hyun, C.; Park, H.

2009-12-01

Tuff is intricately composed of various types of rock blocks and ash matrixes during volcanic formation processes. Qualitative identification and quantitative assessment of mineral composition of tuff usually have been done using manual inspection with naked-eyes and various chemical analyses. Those conventional methods are destructive to objects, time consuming and sometimes carry out biased results from subjective decision making. To overcome limits from conventional methods, assessment technique using reflectance spectroscopy was applied to tuff specimens. Reflectance spectroscopy measures electromagnetic reflectance on rock surface and can extract diagnostic absorption features originated from chemical composition and crystal structure of constituents in the reflectance curve so mineral species can be discriminated qualitatively. The intrinsic absorption feature from particular mineral can be converted to absorption depth representing relative coverage of the mineral in the measurement area by removing delineated convex hull from raw reflectance curve. The spectral measurements were performed with field spectrometer FieldSpec®3 of ASD Inc. and the wavelength range of measurement was form 350nm to 2500nm. Three types of tuff blocks, ash tuff, green lapilli tuff and red lapilli tuff, were sampled from Hwasun County in Korea and the types of tuffs. The differences between green tuff and red tuff are from the color of their matrixes. Ash tuff consists of feldspars and quartz and small amount of chalcedony, calcite, dolomite, epidote and basalt fragments. Green lapilli tuff consists of feldspar, quartz and muscovite and small amount of calcite, chalcedony, sericite, chlorite, quartzite and basalt fragments. Red lapilli tuff consists of feldspar, quartz and muscovite and small amount of calcite, chalcedony, limonite, zircon, chlorite, quartzite and basalt fragments. The tuff rocks were coarsely crushed and blocks and matrixes were separated to measure standard spectral reflectance of each constituent. Unmixing of mineral composition and their weathering products of blocks and matrixes in tuff were conducted and the ratio of mineral composition was calculated for each specimen. This study was supported by National Research Institute of Cultural Heritage (project title: Development on Evaluation Technology for Weathering Degree of Stone Cultural Properties, project no.: 09B011Y-00150-2009).

Recommended nomenclature for zeolite minerals: Report of the Subcommittee on Zeolites of the International Mineralogical Association, Commission on New Minerals and Mineral Names

USGS Publications Warehouse

Coombs, D.S.; Alberti, A.; Armbruster, T.; Artioli, G.; Colella, C.; Galli, E.; Grice, Joel D.; Liebau, F.; Mandarino, J.A.; Minato, H.; Nickel, E.H.; Passaglia, E.; Peacor, D.R.; Quartieri, S.; Rinaldi, R.; Ross, M.; Sheppard, R.A.; Tillmanns, E.; Vezzalini, G.

1998-01-01

This report embodies recommendations on zeolite nomenclature approved by the International Mineralogical Association Commission on New Minerals and Mineral Names. In a working definition of a zeolite mineral used for this review, structures containing an interrupted containing an interrupted framework of tetrahedra are accepted where other zeolitic properties prevail, and complete substitution by elements other than Si and Al is alloowed. Separate species are recognized in topologically distinctive compositional series in which different extra-framework cations are the most abundant in atomic proportions. To name these, the appropriate chemical symbol is attached by a hyphen to the series name as a suffix, except for the names harmotome, pollucite and wairakite in the phillipsite and analcime series. Differences in space-group symmetry and in order-disorder relationships in zeolites having the same topologically distinctive framework do not in general provide adequate grounds for recognition of separate species. Zeolite species are not to be distinguished solely in Si:Al ratio except for heulandite (Si:Al < 4.0) and clinoptilolite (Si:Al ??? 4.0). Dehydration, partial hydration and over-hydration are not sufficient grounds for the recognition of separate species of zeolites. Use of the term 'ideal formula' should be avoided in referring to a simplified or averaged formula of zeolite. Newly recognized species in compositional series are as follows: brewsterite-Sr, -Ba; chabazite-Ca, -Na, -K; clinoptilolite-K, -Na, -Ca; dechiardite-Ca, -Na; erionite-Na, -K, -Ca,; faujasite-Na, -Ca, -Mg; ferrierite-Mg, -K, -Na; gmelinite-Na, -Ca, -K; heulandite-Ca, -Na, -K, -Sr; levyne-Ca, -Na; paulingite-K, -Ca; phillipsite-Na, -Ca, -K stilbite-Ca, -Na. Key references, type locality, origin of name, chemical data, IZA structure-type symbols, space-group symmetry, unit-cell dimensions, and comments on structure are listed for 13 compositional series, 82 accepted zeolite mineral species, and three of doubtful status. Herschelite, leonhardite, svetlozarite and wellsite are discredited as mineral species names. Obsolete and discredited names are listed.

Recommended nomenclature for zeolite minerals: report of the subcommittee on zeolites of the International Mineralogical Association, Commission on new Minerals and Mineral names

USGS Publications Warehouse

Coombs, D.S.; Alberti, A.; Armbruster, T.; Artioli, G.; Colella, C.; Galli, E.; Grice, Joel D.; Liebau, F.; Mandarino, J.A.; Minato, H.; Nickel, E.H.; Passaglia, E.; Peacor, D.R.; Quartieri, S.; Rinaldi, R.; Ross, M.; Sheppard, R.A.; Tillmanns, E.; Vezzalini, G.

1997-01-01

This report embodies recommendations on zeolite nomenclature approved by the International Mineralogical Association, Commission on New Minerals and Mineral Names. In a working definition of a zeolite mineral used for this review, structures containing an interrupted framework of tetrahedra are accepted where other zeolitic properties prevail, and complete substitution by elements other than Si and Al is allowed. Separate species are recognized in topologically distinctive compositional series in which different extra-framework cations are the most abundant in atomic proportions. To name these, the appropriate chemicalsymbol is attached by a hyphen to the series name as a suffix, except for the names harmotome, pollucite and wairakite in the phillipsite and analcime series. Differences in space-group symmetry and in order-disorder relationships in zeolites having the same topologically distinctive framework do not in general provide adequate grounds for recognition of separate species. Zeolite species are not to be distinguished solely on the ratio Si:Al except for heulandite (Si:Al < 4.0) and clinoptilolite (Si:Al ??? 4.0). Dehydration, partial hydration, and overhydration are not sufficient grounds for the recognition of separate species of zeolites. Use of the term 'ideal formula' should be avoided in referring to a simplified or averaged formula of a zeolite. newly recognized species in compositional series are as follows: brewsterite-Sr, -Ba, chabazite-Ca, -Na, -K, clinoptilolite-K, -Na, -Ca, dachiardite-Ca, -Na, erionite-Na, erionite-Na, -K, -Ca, faujasite-Na, -Ca, -Mg, ferrierite-Mg, -K, -Na, gmelinite-Na, -Ca, -K, heulandite-Ca, -Na, -K, -Sr, levyne-Ca, -Na, paulingite-K, -Ca, phillipsite-Na, -Ca, -K, and stilbite-Ca, -Na. Key references, type locality, origin of name, chemical data, IZA structure-type symbols, space-group symmetry, unit-cell dimensions, and comments on structure are listed for 13 compositional series, 82 accepted zeolite mineral species, and three of doubtful status. Herschelite, leonhardite, dvetlozarite, and wellsite are discredited as mineral species names. Obsolete and discredited names are listed.

Molecular simulations and experimental studies of zeolites

NASA Astrophysics Data System (ADS)

Moloy, Eric C.

Zeolites are microporous aluminosilicate tetrahedral framework materials that have symmetric cages and channels with open-diameters between 0.2 and 2.0 nm. Zeolites are used extensively in the petrochemical industries for both their microporosity and their catalytic properties. The role of water is paramount to the formation, structure, and stability of these materials. Zeolites frequently have extra-framework cations, and as a result, are important ion-exchange materials. Zeolites also play important roles as molecular sieves and catalysts. For all that is known about zeolites, much remains a mystery. How, for example, can the well established metastability of these structures be explained? What is the role of water with respect to the formation, stabilization, and dynamical properties? This dissertation addresses these questions mainly from a modeling perspective, but also with some experimental work as well. The first discussion addresses a special class of zeolites: pure-silica zeolites. Experimental enthalpy of formation data are combined with molecular modeling to address zeolitic metastability. Molecular modeling is used to calculate internal surface areas, and a linear relationship between formation enthalpy and internal surface areas is clearly established, producing an internal surface energy of approximately 93 mJ/m2. Nitrate bearing sodalite and cancrinite have formed under the caustic chemical conditions of some nuclear waste processing centers in the United States. These phases have fouled expensive process equipment, and are the primary constituents of the resilient heels in the bottom of storage tanks. Molecular modeling, including molecular mechanics, molecular dynamics, and density functional theory, is used to simulate these materials with respect to structure and dynamical properties. Some new, very interesting results are extracted from the simulation of anhydrous Na6[Si6Al 6O24] sodalite---most importantly, the identification of two distinct oxygen sites (rather than one), and formation of a new supercell. New calorimetric measurements of enthalpy are used to examine the energetics of the hydrosodalite family of zeolites---specifically, formation enthalpies and hydration energies. Finally, force-field computational methods begin the examination of water in terms of energetics, structure, and radionuclide containment and diffusion.

Picrite "Intelligence" from the Middle-Late Triassic Stikine arc: Composition of mantle wedge asthenosphere

NASA Astrophysics Data System (ADS)

Milidragovic, D.; Zagorevski, A.; Weis, D.; Joyce, N.; Chapman, J. B.

2018-05-01

Primitive, near-primary arc magmas occur as a volumetrically minor ≤100 m thick unit in the Canadian Cordillera of northwestern British Columbia, Canada. These primitive magmas formed an olivine-phyric, picritic tuff near the base of the Middle-Late Triassic Stuhini Group of the Stikine Terrane (Stikinia). A new 40Ar/39Ar age on hornblende from a cross-cutting basaltic dyke constrains the tuff to be older than 221 ± 2 Ma. An 87Sr/86Sr isochron of texturally-unmodified tuff samples yields 212 ± 25 Ma age, which is interpreted to represent syn-depositional equilibration with sea-water. Parental trace element magma composition of the picritic tuff is strongly depleted in most incompatible trace elements relative to MORB and implies a highly depleted ambient arc mantle. High-precision trace element and Hf-Nd-Pb isotopic analyses indicate an origin by mixing of a melt of depleted ambient asthenosphere with ≤2% of subducted sediment melt. Metasomatic addition of non-conservative incompatible elements through melting of subducted Panthalassa Ocean floor sediments accounts for the arc signature of the Stuhini Group picritic tuff, enrichment of light rare earth elements (LREE) relative to heavy rare earth elements (HREE) and high field strength elements (HFSE), and anomalous enrichment in Pb. The inferred Panthalassan sediments are similar in composition to the Neogene-Quaternary sediments of the modern northern Cascadia Basin. The initial Hf isotopic composition of the picritic tuff closely approximates that of the ambient Middle-Late Triassic asthenosphere beneath Stikinia and is notably less radiogenic than the age-corrected Hf isotopic composition of the Depleted (MORB) Mantle reservoir (DM or DMM). This suggests that the ambient asthenospheric mantle end-member experienced melt depletion (F ≤ 0.05) a short time before picrite petrogenesis. The mantle end-member in the source of the Stuhini Group picritic tuff is isotopically similar to the mantle source of enriched mid-ocean ridge basalts (E-MORB) erupted today at the southern end of the Explorer Ridge in northeastern Pacific Ocean. The isotopic similarity between the Middle-Late Triassic ambient mantle under Stikinia, and mantle presently tapped at the southern Explorer Ridge suggests that enriched domains in the northeastern Pacific mantle are long-lived (≥222 million years).

In defense of Magnetite-Ilmenite Thermometry in the Bishop Tuff and its implication for gradients in silicic magma reservoirs

USGS Publications Warehouse

Evans, Bernard W; Hildreth, Edward; Bachmann, Olivier; Scaillet, Bruno

2016-01-01

Despite claims to the contrary, the compositions of magnetite and ilmenite in the Bishop Tuff correctly record the changing conditions of T and fO2 in the magma reservoir. In relatively reduced (∆NNO < 1) siliceous magmas (e.g., Bishop Tuff, Taupo units), Ti behaves compatibly (DTi ≈ 2-3.5), leading to a decrease in TiO2 activity in the melt with cooling and fractionation. In contrast, FeTi-oxides are poorer in TiO2 in more oxidized magmas (∆NNO > 1, e.g., Fish Canyon Tuff, Pinatubo), and the d(aTiO2)/dT slope can be negative. Biotite, FeTi-oxides, liquid, and possibly plagioclase largely maintained equilibrium in the Bishop Tuff magma (unlike the pyroxenes, and cores of quartz, sanidine, and zircon) prior ro and during a mixing event triggered by a deeper recharge, which, based on elemental diffusion profiles in minerals, took place at least several decades before eruption. Equilibrating phases and pumice compositions show evolving chemical variations that correlate well with mutually consistent temperatures based on the FeTi-oxides, sanidine-plagioclase, and ∆18O quartz-magnetite pairs. Early Bishop Tuff (EBT) temperatures are lower (700 to ~780‎°C) than temperatures (780 to >820°C) registered in Late Bishop Tuff (LBT), the latter defined here not strictly stratigraphically, but by the presence of orthopyroxene and reverse-zoned rims on quartz and sanidine. The claimed similarity in compositions, Zr-saturation temperatures and thermodynamically calculated temperatures (730-740°C) between EBT and less evolved LBT reflect the use of glass inclusions in quartz cores in LBT that were inherited from the low temperature rhyolitic part of the reservoir characteristic of the EBT. LBT temperatures as high as 820°C, the preservation of orthopyroxene, and the presence of reverse-zoned minerals (quartz, sanidine, zircons) are consistent with magma recharge at the base of the zoned reservoir, heating the cooler rhyolitic melt, partly remelting cumulate mush, and introducing enough CO2 (0.4-1.4 wt%, mostly contained in the exsolved fluid phase) to significantly lower H2O-activity in the system.

Origin of hydrous alkali feldspar-silica intergrowth in spherulites from intra-plate A2-type rhyolites at the Jabal Shama, Saudi Arabia

NASA Astrophysics Data System (ADS)

Surour, Adel A.; El-Nisr, Said A.; Bakhsh, Rami A.

2016-03-01

Miocene rhyolites (19.2 ± 0.9 Ma) at the Jabal Shama in western Saudi Arabia represent an example of rift-related silicic volcanism that took place during the formation of the Red Sea. They mostly consist of tuffaceous varieties with distinct flow banding, and pea-sized spherulites, obsidian and perlitized rhyolite tuffs. Although they have the geochemical signature of A2-type rhyolites, these silicic rocks are not typically alkaline but alkali-calcic to calc-alkaline. They developed in a within-plate regime and possibly derived from a recycled mafic subducted slab in depleted sub-continental mantle beneath the western Arabian plate. The Jabal Shama rhyolites are younger in age than their Miocene counterparts in Yemen and Ethiopia. The Jabal Shama spherulites consist of hydrous alkali feldspar-silica radial intergrowths with an occasional brown glass nucleus. Carbonate- and glass-free spherulites give up to 4.45 wt% L.O.I. The hydrous nature of these silicates and the absence of magnetite in the spherulites is a strong indication of oxidizing conditions. The spherulites contain hydrous feldspars with up to ∼6 wt% H2O, and they develop by diffusion and devitrification of glass in the rhyolite tuff at ∼800 °C. Owing to higher undercooling due to supersaturation, the radial hydrous phases within spherulites might grow faster and led to coagulation. The polygonal contacts between spherulites and the ∼120° dihedral angle suggest solid-state modification and recrystallization as the process of devitrification proceeds as low as ∼300 °C. The sum of FeO + MgO is positively correlated with total alkalies along with magnetite oxidation in the matrix to Fe-oxyhydroxides, and to the incorporation of OH- into silicates within the spehrulites themselves. Structural H2O in glass of the Jabal Shama perlite (obsidian) is considerable (∼9-12 wt%) with 3.72-5.6 wt% L.O.I. of the whole-rock. The presence of deleterious silica impurities would lower the ore grade due to poor expansion. Zeolitization of the rhyolite tuff was limited or incomplete in comparison with that of Pliocene-Pleistocene rift-related mafic volcanics in the western Arabian plate.

Polynomials for crystal frameworks and the rigid unit mode spectrum

PubMed Central

Power, S. C.

2014-01-01

To each discrete translationally periodic bar-joint framework in , we associate a matrix-valued function defined on the d-torus. The rigid unit mode (RUM) spectrum of is defined in terms of the multi-phases of phase-periodic infinitesimal flexes and is shown to correspond to the singular points of the function and also to the set of wavevectors of harmonic excitations which have vanishing energy in the long wavelength limit. To a crystal framework in Maxwell counting equilibrium, which corresponds to being square, the determinant of gives rise to a unique multi-variable polynomial . For ideal zeolites, the algebraic variety of zeros of on the d-torus coincides with the RUM spectrum. The matrix function is related to other aspects of idealized framework rigidity and flexibility, and in particular leads to an explicit formula for the number of supercell-periodic floppy modes. In the case of certain zeolite frameworks in dimensions two and three, direct proofs are given to show the maximal floppy mode property (order N). In particular, this is the case for the cubic symmetry sodalite framework and some other idealized zeolites. PMID:24379422

Self-assembly in poly(dimethylsiloxane)-poly(ethylene oxide) block copolymer template directed synthesis of Linde type A zeolite.

PubMed

Bonaccorsi, Lucio; Calandra, Pietro; Kiselev, Mikhail A; Amenitsch, Heinz; Proverbio, Edoardo; Lombardo, Domenico

2013-06-11

We describe the hydrothermal synthesis of zeolite Linde type A (LTA) submicrometer particles using a water-soluble amphiphilic block copolymer of poly(dimethylsiloxane)-b-poly(ethylene oxide) as a template. The formation and growth of the intermediate aggregates in the presence of the diblock copolymer have been monitored by small-angle X-ray scattering (SAXS) above the critical micellar concentration at a constant temperature of 45 °C. The early stage of the growth process was characterized by the incorporation of the zeolite LTA components into the surface of the block copolymer micellar aggregates with the formation of primary units of 4.8 nm with a core-shell morphology. During this period, restricted to an initial time of 1-3 h, the core-shell structure of the particles does not show significant changes, while a subsequent aggregation process among these primary units takes place. A shape transition of the SAXS profile at the late stage of the synthesis has been connected with an aggregation process among primary units that leads to the formation of large clusters with fractal characteristics. The formation of large supramolecular assemblies was finally verified by scanning electron microscopy, which evidenced the presence of submicrometer aggregates with size ranging between 100 and 300 nm, while X-ray diffraction confirmed the presence of crystalline zeolite LTA. The main finding of our results gives novel insight into the mechanism of formation of organic-inorganic mesoporous materials based on the use of a soft interacting nanotemplate as well as stimulates the investigation of alternative protocols for the synthesis of novel hybrid materials with new characteristics and properties.

Welded tuff porosity characterization using mercury intrusion, nitrogen and ethylene glycol monoethyl ether sorption and epifluorescence microscopy

USGS Publications Warehouse

Reddy, M.M.; Claassen, H.C.; Rutherford, D.W.; Chiou, C.T.

1994-01-01

Porosity of welded tuff from Snowshoe Mountain, Colorado, was characterized by mercury intrusion porosimetry (MIP), nitrogen sorption porosimetry, ethylene glycol monoethyl ether (EGME) gas phase sorption and epifluorescence optical microscopy. Crushed tuff of two particle-size fractions (1-0.3 mm and less than 0.212 mm), sawed sections of whole rock and crushed tuff that had been reacted with 0.1 N hydrochloric acid were examined. Average MIP pore diameter values were in the range of 0.01-0.02??m. Intrusion volume was greatest for tuff reacted with 0.1 N hydrochloric acid and least for sawed tuff. Cut rock had the smallest porosity (4.72%) and crushed tuff reacted in hydrochloric acid had the largest porosity (6.56%). Mean pore diameters from nitrogen sorption measurements were 0.0075-0.0187 ??m. Nitrogen adsorption pore volumes (from 0.005 to 0.013 cm3/g) and porosity values (from 1.34 to 3.21%) were less than the corresponding values obtained by MIP. More than half of the total tuff pore volume was associated with pore diameters < 0.05??m. Vapor sorption of EGME demonstrated that tuff pores contain a clay-like material. Epifluorescence microscopy indicated that connected porosity is heterogeneously distributed within the tuff matix; mineral grains had little porosity. Tuff porosity may have important consequences for contaminant disposal in this host rock. ?? 1994.

Pretest thermal analysis of the Tuff Water Migration/In-Situ Heater Experiment

DOE Office of Scientific and Technical Information (OSTI.GOV)

Bulmer, B.M.

This report describes the pretest thermal analysis for the Tuff Water Migration/In-Situ Heater Experiment to be conducted in welded tuff in G-tunnel, Nevada Test Site. The parametric thermal modeling considers variable boiling temperature, tuff thermal conductivity, tuff emissivity, and heater operating power. For nominal tuff properties, some near field boiling is predicted for realistic operating power. However, the extent of boiling will be strongly determined by the ambient (100% water saturated) rock thermal conductivity. In addition, the thermal response of the heater and of the tuff within the dry-out zone (i.e., bounded by boiling isotherm) is dependent on the temperaturemore » variation of rock conductivity as well as the extent of induced boiling.« less

Petrology, sedimentology, and diagenesis of hemipelagic limestone and tuffaceous turbidities in the Aksitero Formation, central Luzon, Philippines

USGS Publications Warehouse

Garrison, Robert E.; Espiritu, E.; Horan, L.J.; Mack, L.E.

1979-01-01

The Aksitero Formation of central Luzon is an upper Eocene and lower Oligocene sequence of evenly bedded hemipelagic limestone with a few thin interlayers of tuffaceous turbidites. The limestone consists chiefly of planktonic foraminifers and calcareous nannofossils, with up to 30 percent of noncarbonate components, chiefly volcaniclastic debris. The tuff layers are graded beds. Composed mainly of glass shards, pumice fragments, crystals, and fine-grained volcanic rock fragments. Hydrocarbons migrated into the pores of the tuffaceous layers early during diagenesis but they were subsequently flushed out and only bitumen remains, chiefly as thin coatings on grains and wthin pumice vesicles. Later during diagenesis, zeolites (mordenite and c1inoptilolite) and secondary calcite preferentially replaced glass shards and pumice fragments. Deposition of the Aksitero Formation probably occurred at depths of at least 1,000 meters within a subsiding basin adjacent to an active island arc system. Submarine ash eruptions of silicic composition caused volcaniclastic turbidity currents that occasionally reached the basin floor. The more proximal facies of these volcaniclastic deposits may be prospective for hydrocarbons.

Revised stratigraphy of Area 123, Koobi Fora, Kenya, and new age estimates of its fossil mammals, including hominins.

PubMed

Gathogo, Patrick N; Brown, Francis H

2006-11-01

Recent geologic study shows that all hominins and nearly all other published mammalian fossils from Paleontological Collection Area 123, Koobi Fora, Kenya, derive from levels between the KBS Tuff (1.87+/-0.02 Ma) and the Lower Ileret Tuff (1.53+/-0.01 Ma). More specifically, the fossils derive from 53 m of section below the Lower Ileret Tuff, an interval in which beds vary markedly laterally, especially those units containing molluscs and algal stromatolites. The upper Burgi Member (approximately 2.00-1.87 Ma) crops out only in the southwestern part of Area 123. Adjacent Area 110 contains larger exposures of the member, and there the KBS Tuff is preserved as an airfall ash in lacustrine deposits and also as a fluvially redeposited ash. We observed no mammalian fossils in situ in this member in Area 123, but surface specimens have been documented in some monographic treatments. Fossil hominins from Area 123 were attributed to strata above the KBS Tuff in the 1970s, but later they were assigned to strata below the KBS Tuff (now called the upper Burgi Member). This study definitively places the Area 123 hominins in the KBS Member. Most of these hominins are between 1.60 and 1.65 myr in age, but the youngest may date to only 1.53 Ma, and the oldest, to 1.75 Ma. All are 0.15-0.30 myr younger than previously estimated. The new age estimates, in conjunction with published taxonomic attributions of fossils, suggest that at least two species of Homo coexisted in the region along with A. boisei until at least 1.65 Ma. Comparison of crania KNM-ER 1813 and KNM-ER 1470, which were believed to be of comparable age, is at the focus of the debate over whether Homo habilis sensu lato is in fact composed of two species: Homo habilis and Homo rudolfensis. These two crania are separated in time by approximately 0.25 myr, and therefore, arguments for their conspecificity no longer need to confront the issue of unusually high contemporaneous variation within a single species.

Cutting Materials in Half: A Graph Theory Approach for Generating Crystal Surfaces and Its Prediction of 2D Zeolites

DOE Office of Scientific and Technical Information (OSTI.GOV)

Witman, Matthew; Ling, Sanliang; Boyd, Peter

Scientific interest in two-dimensional (2D) materials, ranging from graphene and other single layer materials to atomically thin crystals, is quickly increasing for a large variety of technological applications. While in silico design approaches have made a large impact in the study of 3D crystals, algorithms designed to discover atomically thin 2D materials from their parent 3D materials are by comparison more sparse. Here, we hypothesize that determining how to cut a 3D material in half (i.e., which Miller surface is formed) by severing a minimal number of bonds or a minimal amount of total bond energy per unit area canmore » yield insight into preferred crystal faces. We answer this question by implementing a graph theory technique to mathematically formalize the enumeration of minimum cut surfaces of crystals. While the algorithm is generally applicable to different classes of materials, we focus on zeolitic materials due to their diverse structural topology and because 2D zeolites have promising catalytic and separation performance compared to their 3D counterparts. We report here a simple descriptor based only on structural information that predicts whether a zeolite is likely to be synthesizable in the 2D form and correctly identifies the expressed surface in known layered 2D zeolites. The discovery of this descriptor allows us to highlight other zeolites that may also be synthesized in the 2D form that have not been experimentally realized yet. Finally, our method is general since the mathematical formalism can be applied to find the minimum cut surfaces of other crystallographic materials such as metal-organic frameworks, covalent-organic frameworks, zeolitic-imidazolate frameworks, metal oxides, etc.« less

Cutting Materials in Half: A Graph Theory Approach for Generating Crystal Surfaces and Its Prediction of 2D Zeolites.

PubMed

Witman, Matthew; Ling, Sanliang; Boyd, Peter; Barthel, Senja; Haranczyk, Maciej; Slater, Ben; Smit, Berend

2018-02-28

Scientific interest in two-dimensional (2D) materials, ranging from graphene and other single layer materials to atomically thin crystals, is quickly increasing for a large variety of technological applications. While in silico design approaches have made a large impact in the study of 3D crystals, algorithms designed to discover atomically thin 2D materials from their parent 3D materials are by comparison more sparse. We hypothesize that determining how to cut a 3D material in half (i.e., which Miller surface is formed) by severing a minimal number of bonds or a minimal amount of total bond energy per unit area can yield insight into preferred crystal faces. We answer this question by implementing a graph theory technique to mathematically formalize the enumeration of minimum cut surfaces of crystals. While the algorithm is generally applicable to different classes of materials, we focus on zeolitic materials due to their diverse structural topology and because 2D zeolites have promising catalytic and separation performance compared to their 3D counterparts. We report here a simple descriptor based only on structural information that predicts whether a zeolite is likely to be synthesizable in the 2D form and correctly identifies the expressed surface in known layered 2D zeolites. The discovery of this descriptor allows us to highlight other zeolites that may also be synthesized in the 2D form that have not been experimentally realized yet. Finally, our method is general since the mathematical formalism can be applied to find the minimum cut surfaces of other crystallographic materials such as metal-organic frameworks, covalent-organic frameworks, zeolitic-imidazolate frameworks, metal oxides, etc.

Cutting Materials in Half: A Graph Theory Approach for Generating Crystal Surfaces and Its Prediction of 2D Zeolites

PubMed Central

2018-01-01

Scientific interest in two-dimensional (2D) materials, ranging from graphene and other single layer materials to atomically thin crystals, is quickly increasing for a large variety of technological applications. While in silico design approaches have made a large impact in the study of 3D crystals, algorithms designed to discover atomically thin 2D materials from their parent 3D materials are by comparison more sparse. We hypothesize that determining how to cut a 3D material in half (i.e., which Miller surface is formed) by severing a minimal number of bonds or a minimal amount of total bond energy per unit area can yield insight into preferred crystal faces. We answer this question by implementing a graph theory technique to mathematically formalize the enumeration of minimum cut surfaces of crystals. While the algorithm is generally applicable to different classes of materials, we focus on zeolitic materials due to their diverse structural topology and because 2D zeolites have promising catalytic and separation performance compared to their 3D counterparts. We report here a simple descriptor based only on structural information that predicts whether a zeolite is likely to be synthesizable in the 2D form and correctly identifies the expressed surface in known layered 2D zeolites. The discovery of this descriptor allows us to highlight other zeolites that may also be synthesized in the 2D form that have not been experimentally realized yet. Finally, our method is general since the mathematical formalism can be applied to find the minimum cut surfaces of other crystallographic materials such as metal–organic frameworks, covalent-organic frameworks, zeolitic-imidazolate frameworks, metal oxides, etc. PMID:29532024

Cutting Materials in Half: A Graph Theory Approach for Generating Crystal Surfaces and Its Prediction of 2D Zeolites

DOE PAGES

Witman, Matthew; Ling, Sanliang; Boyd, Peter; ...

2018-02-06

Scientific interest in two-dimensional (2D) materials, ranging from graphene and other single layer materials to atomically thin crystals, is quickly increasing for a large variety of technological applications. While in silico design approaches have made a large impact in the study of 3D crystals, algorithms designed to discover atomically thin 2D materials from their parent 3D materials are by comparison more sparse. Here, we hypothesize that determining how to cut a 3D material in half (i.e., which Miller surface is formed) by severing a minimal number of bonds or a minimal amount of total bond energy per unit area canmore » yield insight into preferred crystal faces. We answer this question by implementing a graph theory technique to mathematically formalize the enumeration of minimum cut surfaces of crystals. While the algorithm is generally applicable to different classes of materials, we focus on zeolitic materials due to their diverse structural topology and because 2D zeolites have promising catalytic and separation performance compared to their 3D counterparts. We report here a simple descriptor based only on structural information that predicts whether a zeolite is likely to be synthesizable in the 2D form and correctly identifies the expressed surface in known layered 2D zeolites. The discovery of this descriptor allows us to highlight other zeolites that may also be synthesized in the 2D form that have not been experimentally realized yet. Finally, our method is general since the mathematical formalism can be applied to find the minimum cut surfaces of other crystallographic materials such as metal-organic frameworks, covalent-organic frameworks, zeolitic-imidazolate frameworks, metal oxides, etc.« less

Geochemistry of rock units at the potential repository level, Yucca Mountain, Nevada

USGS Publications Warehouse

Peterman, Z.E.; Cloke, P.L.

2002-01-01

The compositional variability of the phenocryst-poor member of the 12.8 Ma Topopah Spring Tuff at the potential repository level was assessed by duplicate analysis of 20 core samples from the cross drift at Yucca Mountain, Nevada. Previous analyses of outcrop and core samples of the Topopah Spring Tuff showed that the phenocryst-poor rhyolite, which includes both lithophysal and nonlithophysal zones, is relatively uniform in composition. Analyses of rock samples from the cross drift, the first from the actual potential repository block, also indicate the chemical homogeneity of this unit excluding localized deposits of vapor-phase minerals and low-temperature calcite and opal in fractures, cavities, and faults. The possible influence of vapor-phase minerals and calcite and opal coatings on rock composition at a scale sufficiently large to incorporate these heterogeneously distributed deposits was evaluated and is considered to be relatively minor. Therefore, the composition of the phenocryst-poor member of the Topopah Spring Tuff is considered to be adequately represented by the analyses of samples from the cross drift. The mean composition as represented by the 10 most abundant oxides in wt. % or g/100 g is: SiO2, 76.29; Al2O3, 12.55; FeO, 0.14; Fe2O3, 0.97; MgO, 0.13; CaO, 0.50; Na2O, 3.52; K2O, 4.83; TiO2, 0.11; and MnO, 0.07. ?? 2002 Published by Elsevier Science Ltd.

Geohydrologic and drill-hole data for test well USW H-4, Yucca Mountain, Nye County, Nevada

DOE Office of Scientific and Technical Information (OSTI.GOV)

Whitfield, M.S. Jr.; Thordarson, W.; Eshom, E.P.

This report presents data on drilling operations, lithology, geophysical well logs, sidewall-core samples, water-level monitoring, pumping tests, injection tests, radioactive-tracer borehole flow survey, and water chemistry for test well USW H-4. The well is one of a series of test wells drilled in the southwestern part of the Nevada Test Site, Nye County, Nevada, in cooperation with the US Department of Energy. These test wells are part of the Nevada Nuclear Waste Storage Investigations to identify sites for storage of high-level radioactive wastes. Test well USW H-4 was drilled in ash-flow tuff to a total depth of 1219 meters. Depthmore » to water below land surface was 519 meters, or at an altitude of 730 meters above sea level. After test pumping at a rate of 17.4 liters per second for approximately 9 days, the drawdown was 4.85 meters. A radioactive borehole-flow survey indicated that the Bullfrog Member of the Crater Flat Tuff (Tertiary age) was the most productive geologic unit, producing 36.5 percent of the water in the well. The second most productive geologic unit was the Tram Member of the Crater Flat Tuff, which produced 32 percent of the water. The water in test well USW H-4 is predominantly a soft, sodium bicarbonate type of water typical of water produced in tuffaceous rocks in southern Nevada. 7 references, 26 figures, 9 tables.« less

Fault evolution in volcanic tuffs and quartz-rich eolian sandstone as mechanical analogs for faulting in Martian pyroclastic deposits

NASA Astrophysics Data System (ADS)

Okubo, C. H.

2014-12-01

In order to establish a foundation for studies of faulting in Martian rocks and soils in volcanic terrain, the distribution of brittle strain around faults within the North Menan Butte Tuff in the eastern Snake River Plain, Idaho and the Joe Lott Tuff Member of the Mount Belknap Volcanics, Utah, has been recently described. These studies employed a combination of macroscopic and microscopic observations, including measurements of in situ permeability as a proxy for non-localized brittle deformation of the host rock. In areas where the tuff retained its primary granular nature at the time of deformation, initial plastic yielding in both tuffs occurred along deformation bands. Both compactional and dilational types of deformation bands were observed, and faulting occurred along clusters of deformation bands. Where secondary alteration processes imparted a massive texture to the tuff, brittle deformation was accommodated along fractures. Host-rock permeability exhibits little variation from non-deformed values in the North Menan Butte Tuff, whereas host rock permeability is reduced by roughly an order of magnitude through compaction alone (no alteration) in the Joe Lott Tuff. To create a bridge between these observations in tuff and the more substantial body of work centered on deformation band formation and faulting in quartz-rich sandstones, the same techniques employed in the North Menan Butte Tuff and the Joe Lott Tuff have also been applied to a kilometer-scale fault in the Jurassic Navajo Sandstone in the Waterpocket Fold, Utah. These observations demonstrate that the manifestation of strain and evolution of faulting in the Mars-analog tuffs are comparable to that in quartz-rich sandstones. Therefore, current understanding of brittle deformation in quartz-rich sandstones can be used to inform investigations into fault growth within porous tuffs on Mars. A discussion of these observations, practical limitations, and directions for future work are presented here.

Revised ages for tuffs of the Yellowstone Plateau volcanic field: Assignment of the Huckleberry Ridge Tuff to a new geomagnetic polarity event

USGS Publications Warehouse

Lanphere, M.A.; Champion, D.E.; Christiansen, R.L.; Izett, G.A.; Obradovich, J.D.

2002-01-01

40Ar/39Ar ages were determined on the three major ash-flow tuffs of the Yellowstone Plateau volcanic field in the region of Yellowstone National Park in order to improve the precision of previously determined ages. Total-fusion and incremental-heating ages of sanidine yielded the following mean ages: Huckleberry Ridge Tuff-2.059 ?? 0.004 Ma; Mesa Falls Tuff-1.285 ?? 0.004 Ma; and Lava Creek Tuff-0.639 ?? 0.002 Ma. The Huckleberry Ridge Tuff has a transitional magnetic direction and has previously been related to the Reunion Normal-Polarity Subchron. Dating of the Reunion event has been reviewed and its ages have been normalized to a common value for mineral standards. The age of the Huckleberry Ridge Tuff is significantly younger than lava flows of the Reunion event on Re??union Island, supporting other evidence for a normal-polarity event younger than the Reunion event.

The oligocene Lund Tuff, Great Basin, USA: A very large volume monotonous intermediate

USGS Publications Warehouse

Maughan, L.L.; Christiansen, E.H.; Best, M.G.; Gromme, C.S.; Deino, A.L.; Tingey, D.G.

2002-01-01

Unusual monotonous intermediate ignimbrites consist of phenocryst-rich dacite that occurs as very large volume (> 1000 km3) deposits that lack systematic compositional zonation, comagmatic rhyolite precursors, and underlying plinian beds. They are distinct from countless, usually smaller volume, zoned rhyolite-dacite-andesite deposits that are conventionally believed to have erupted from magma chambers in which thermal and compositional gradients were established because of sidewall crystallization and associated convective fractionation. Despite their great volume, or because of it, monotonous intermediates have received little attention. Documentation of the stratigraphy, composition, and geologic setting of the Lund Tuff - one of four monotonous intermediate tuffs in the middle-Tertiary Great Basin ignimbrite province - provides insight into its unusual origin and, by implication, the origin of other similar monotonous intermediates. The Lund Tuff is a single cooling unit with normal magnetic polarity whose volume likely exceeded 3000 km3. It was emplaced 29.02 ?? 0.04 Ma in and around the coeval White Rock caldera which has an unextended north-south diameter of about 50 km. The tuff is monotonous in that its phenocryst assemblage is virtually uniform throughout the deposit: plagioclase > quartz ??? hornblende > biotite > Fe-Ti oxides ??? sanidine > titanite, zircon, and apatite. However, ratios of phenocrysts vary by as much as an order of magnitude in a manner consistent with progressive crystallization in the pre-eruption chamber. A significant range in whole-rock chemical composition (e.g., 63-71 wt% SiO2) is poorly correlated with phenocryst abundance. These compositional attributes cannot have been caused wholly by winnowing of glass from phenocrysts during eruption, as has been suggested for the monotonous intermediate Fish Canyon Tuff. Pumice fragments are also crystal-rich, and chemically and mineralogically indistinguishable from bulk tuff. We postulate that convective mixing in a sill-like magma chamber precluded development of a zoned chamber with a rhyolitic top or of a zoned pyroclastic deposit. Chemical variations in the Lund Tuff are consistent with equilibrium crystallization of a parental dacitic magma followed by eruptive mixing of compositionally diverse crystals and high-silica rhyolite vitroclasts during evacuation and emplacement. This model contrasts with the more systematic withdrawal from a bottle-shaped chamber in which sidewall crystallization creates a marked vertical compositional gradient and a substantial volume of capping-evolved rhyolite magma. Eruption at exceptionally high discharge rates precluded development of an underlying plinian deposit. The generation of the monotonous intermediate Lund magma and others like it in the middle Tertiary of the western USA reflects an unusually high flux of mantle-derived mafic magma into unusually thick and warm crust above a subducting slab of oceanic lithosphere. ?? 2002 Elsevier Science B.V. All rights reserved.

Chronology of early Archaean granite-greenstone evolution in the Barberton Mountain Land, South Africa, based on precise dating by single zircon evaporation

NASA Technical Reports Server (NTRS)

Kruener, Alfred; Byerly, Gary R.; Lowe, Donald R.

1991-01-01

Precise Pb-207/Pb-206 single zircon evaporating ages are reported for low-grade felsic metavolcanic rocks within the Onverwacht and Fig Tree Groups of the Barberton Greenstone Belt (BGB), South Africa, as well as for granitoid plutons bordering the belt. Dacitic tuffs of the Hooggenoeg Formation in the upper part of the Onverwacht Group are shown to yield ages between 3445 + or - 3 and 3416 + or - 5 Ma and to contain older crustal components represented by a 3504 + or - 4 Ma old zircon xenocryst. Fig Tree dacitic tuffs and agglomerates have euhedral zircons between 3259 + or - 3 Ma in age which are interpreted to reflect the time of crystallization. The comagmatic relationships between greenstone felsic volcanic units and the surrounding plutonic suites are keynoted. The data adduced show that the Onverwacht and Fig Tree felsic units have distinctly different ages and thus do not constitute a single, tectonically repeated unit as proposed by others. It is argued that conventional multigrain zircon dating may not accurately identify the time of felsic volcanic activity in ancient greenstones, and that the BGB in the Kaapval craton of southern Africa and greenstones in the Pilbara Block of Western Australia may have been part of a larger crustal unit in early Archaean times.

An investigation of volcanic depressions. Part 3: Maars, tuff-rings, tuff-cones, and diatremes

NASA Technical Reports Server (NTRS)

Lorenz, V.; Mcbirney, A. R.; Williams, H.

1970-01-01

A classification of maars, tuff-rings, tuff-cones, and diatremes is given along with a summary of their lithologic and structural characteristics at the surface and at depth, and their probable manner of formation. Particular emphasis is placed on the roles of fluidization and groundwater.

Microgravity

NASA Image and Video Library

1992-06-25

Space Shuttle Columbia (STS-50) astronaut Bornie Dunbar wears protective goggles to assemble a zeolite sample cartridge for the Crystal Growth Furnace (CGF) in the United States Microgravity Laboratory-1 (USML-1) science module.

Template-Based Geometric Simulation of Flexible Frameworks

PubMed Central

Wells, Stephen A.; Sartbaeva, Asel

2012-01-01

Specialised modelling and simulation methods implementing simplified physical models are valuable generators of insight. Template-based geometric simulation is a specialised method for modelling flexible framework structures made up of rigid units. We review the background, development and implementation of the method, and its applications to the study of framework materials such as zeolites and perovskites. The “flexibility window” property of zeolite frameworks is a particularly significant discovery made using geometric simulation. Software implementing geometric simulation of framework materials, “GASP”, is freely available to researchers. PMID:28817055

Age, composition, and areal distribution of the Pliocene Lawlor Tuff, and three younger Pliocene tuffs, California and Nevada

USGS Publications Warehouse

Sarna-Wojcicki, Andrei M.; Deino, Alan L.; Fleck, Robert J.; McLaughlin, Robert J.; Wagner, David; Wan, Elmira; Wahl, David B.; Hillhouse, John W.; Perkins, Michael

2011-01-01

The Lawlor Tuff is a widespread dacitic tephra layer produced by Plinian eruptions and ash flows derived from the Sonoma Volcanics, a volcanic area north of San Francisco Bay in the central Coast Ranges of California, USA. The younger, chemically similar Huichica tuff, the tuff of Napa, and the tuff of Monticello Road sequentially overlie the Lawlor Tuff, and were erupted from the same volcanic field. We obtain new laser-fusion and incremental-heating 40Ar/39Ar isochron and plateau ages of 4.834 ± 0.011, 4.76 ± 0.03, ≤4.70 ± 0.03, and 4.50 ± 0.02 Ma (1 sigma), respectively, for these layers. The ages are concordant with their stratigraphic positions and are significantly older than those determined previously by the K-Ar method on the same tuffs in previous studies.Based on offsets of the ash-flow phase of the Lawlor Tuff by strands of the eastern San Andreas fault system within the northeastern San Francisco Bay area, total offset east of the Rodgers Creek–Healdsburg fault is estimated to be in the range of 36 to 56 km, with corresponding displacement rates between 8.4 and 11.6 mm/yr over the past ∼4.83 Ma.We identify these tuffs by their chemical, petrographic, and magnetic characteristics over a large area in California and western Nevada, and at a number of new localities. They are thus unique chronostratigraphic markers that allow correlation of marine and terrestrial sedimentary and volcanic strata of early Pliocene age for their region of fallout. The tuff of Monticello Road is identified only near its eruptive source.

Alteration mineralogy, mineral chemistry and stable isotope geochemistry of the Eocene pillow lavas from the Trabzon area, NE Turkey

NASA Astrophysics Data System (ADS)

Abdioğlu Yazar, Emel

2018-02-01

The Eocene subaqueous volcanic units in NE Turkey developed as pillow, closely packed pillow, isolated pillow, pillow breccia, hyaloclastite breccia and rare peperitic facies with red micritic limestones. They are locally set on volcaniclastic sandstone and claystone alternations and gradually pass to tuffs and volcanic breccias. The pillow lava samples generally exhibit intersertal, intergranular, microlitic porphyritic, variolitic, vesicular and glomeroporphyritic and glassy textures with clinopyroxene (Wo47-52En40-45Fs6-8), plagioclase (An10 to An96), olivine (Fo79-87) and Fe-Ti oxides (Usp0-0.27). Saponite, interlayered chlorite/saponite, rare beidellite and calcite were determined after olivine, rarely after plagioclase as well as in the glassy groundmass. Illite was restricted to plagioclase and the glassy groundmass. Na-Ca zeolites, chlorites/saponites, beidellite, dolomite and calcite occur as void infillings and in the glassy groundmass. Mineralogical, lithochemical and isotopic interpretations as well as thermometric calculations reveal a low-temperature seawater alteration in a semi-closed environment for the alteration of primary minerals and volcanic glass in addition to sealed vesicles and open systems for crosscutting veins. Due to the short exposure time intervals of seawater to rocks, the total chemistry of the rocks is not fully changed and most of the elements seem to be immobile, remaining in the system as a result of precipitation in voids and cracks. Thermometric estimations indicate that, the temperature of heated seawater is approximately 160 °C at the highest point especially in the vesicles, and decreases to approximately 85 °C due to circulation, resulting in alterations of the primary phases and volcanic glass.

Synthesis and Properties of Nanoparticle Forms Saponite Clay, Cancrinite Zeolite and Phase Mixtures Thereof.

PubMed

Shao, Hua; Pinnavaia, Thomas J

2010-09-01

The low-temperature synthesis (90°C) of nanoparticle forms of a pure phase smectic clay (saponite) and zeolite (cancrinite) is reported, along with phase mixtures thereof. A synthesis gel corresponding to the Si:Al:Mg unit cell composition of saponite (3.6:0.40:3.0) and a NaOH/Si ratio of 1.39 affords the pure phase clay with disordered nanolayer stacking. Progressive increases in the NaOH/Si ratio up to a value of 8.33 results in the co-crystallization of first garronite and then cancrinite zeolites with nanolath morphology. The resulting phase mixtures exhibit a compound particulate structure of intertwined saponite nanolayers and cancrinite nanolaths that cannot be formed through physical mixing of the pure phase end members. Under magnesium-free conditions, pure phase cancrinite nanocrystals are formed. The Si/Al ratio of the reaction mixture affects the particle morphology as well as the chemical composition of the cancrinite zeolite. Ordinarily, cancrinite crystallizes with a Si/Al ratio of 1.0, but a silicon-rich form of the zeolite (Si/Al=1.25) is crystallized at low temperature from a silica rich synthesis gel, as evidenced by (29)Si NMR spectroscopy and XEDS-TEM. Owing to the exceptionally high external surface areas of the pure phase clay (875 m(2)/g) and zeolite end members (8.9 - 40 m(2)/g), as well as their unique mixed phase composites (124 - 329 m(2)/g), these synthetic derivatives are promising model nanoparticles for studies of the bioavailability of poly-aromatic hydrocarbons immobilized in silicate bearing sediments and soils.

Unraveling the volcanic and post-volcanic history at Upsal Hogback, Fallon, Nevada, USA

NASA Astrophysics Data System (ADS)

Anderson, E.; Cousens, B.

2013-12-01

Upsal Hogback is a < 25 ka phreatomagmatic volcanic center situated near Fallon, Nevada. The volcano neighbors two other young volcanic complexes: the Holocene Soda Lakes maars and Rattlesnake Hill, a ~ 1 Ma volcanic neck (Shevenell et al., 2005). These volcanoes lie on the transition between the Sierra Nevada and the Basin and Range province, as well as on the edge of the Walker Lane. Upsal Hogback includes two to four vents, fewer than mapped by Morrison (1964), and can be divided into north (one vent) and south (three potential vents) complexes. The vents all produced phreatomagmatic eruptions resulting in tuff rings composed primarily of coarse, indurated lapilli tuffs with abundant volcanic bombs. Ash tuffs are infrequent, as are structures such as crossbedding. The bombs and lapilli include olivine and plagioclase phenocrysts. The basalts are alkaline and have intraplate-type normalized incompatible element patterns. Both complexes are enriched in LREE compared to HREE, though the north complex overall has lower concentrations of the REE. The flat HREE pattern is indicative of spinel peridotite mantle source. Epsilon Nd values for the north complex are +2.50+/-0.02 and for the south complex are +2.83+/-0.02. The magmas appear to have an enriched asthenospheric mantle source. Bomb samples show that eruptions from the two complexes are geochemically distinguishable both in major and trace elements, suggesting that the two complexes tapped different magma types during eruptions that likely occurred at slightly different times. The proximity of Upsal Hogback to Fallon makes constraining its age important to characterize the hazard to the city. It lies above the Wono ash bed, dated at 25,000 years (Fultz et al., 1983), and tufa deposited over the edifice is dated at 11,100 +/- 100 and 8,600 +/- 200 years (Benson et al., 1992; Broecker and Kaufman, 1965). 40Ar/39Ar total gas age by Shevenell et al. (2005) dated the volcano at 0.60 +/- 0.09 Ma, but with no plateau or isochron, and is thus unreliable. The ash bed and tufa ages show that the eruptions would have occurred during the late history of glacial Lake Lahontan. The evidence for primarily subaerial or shallow subaqueous eruptions, including abundant bomb sags and armored lapilli, demonstrate that most of the volcanism occurred during a low stand in lake level history. Some upper tuff units have been heavily altered to palagonite, which establishes that there was substantial water present during some of the later eruptions. The upper edifice has been significantly modified by slumping of the lapilli tuffs during or after of the eruptions, as indicated by the wildly varying strikes and dips found in adjacent lapilli tuff blocks. Lake Lahontan has substantially altered the morphology of the volcano through wave action and shoreline erosion, as well as tufa deposition, since the eruption and emplacement of the tuffs. The edifice has gone through significant changes during its post-eruptive history that mask many of its original features; it was possible that it was a tuff cone that has been modified into a tuff ring.

A summary of the geology and petrology of the Sierra La Primavera, Jalisco, Mexico

NASA Astrophysics Data System (ADS)

Mahood, Gail A.

1981-11-01

The Sierra La Primavera, near Guadalajara, Mexico, is a Late Pleistocene rhyolitic center consisting of lava flows and domes, ash flow tuff, air fall pumice, and caldera lake sediments. All eruptive units are high-silica rhyolites, but systematic compositional differences correlate with age and eruptive mode. The earliest lavas erupted approximately 145,000 years ago and were followed approximately 95,000 years ago by the eruption of about 20 km3 of magma as ash flows that form the Tala Tuff. The Tala Tuff is zoned from a mildly peralkaline first-erupted portion enriched in Na, Rb, Cs, Cl, F, Zn, Y, Zr, Nb, Sb, HREE, Hf, Ta, Pb, Th, and U to a metaluminous last-erupted part enriched in K, LREE, Sc, and Ti; Al, Ca, Mg, Mn, Fe, and Eu are constant within analytical errors. Collapse of the roof zone of the magma chamber led to the formation of a shallow 11-km-diameter caldera in which lake sediments began to collect. The earliest postcaldera lava, the south-central dome, is nearly identical to the last-erupted portion of the Tala Tuff, whereas the slightly younger north-central dome is chemically transitional from the south-central dome to later, more mafic, ring domes. This sequence of ash flow tuff and domes represents the tapping of progressively deeper levels of a zoned magma chamber 95,000 ± 5,000 years ago. Sedimentation continued and a period of volcanic quiescence was marked by the deposition of some 30 m of fine-grained ashy sediments. Approximately 75,000 years ago a new group of ring domes erupted at the southern margin of the lake. These domes are lapped by only 10-20 m of sediments as uplift resulting from renewed insurgence of magma brought an end to the lake. This uplift culminated in the eruption, beginning approximately 60,000 years ago, of aphyric lavas along a southern arc. The youngest of these lavas erupted approximately 30,000 years ago. The lavas that erupted 75,000, 60,000, and 30,000 years ago became decreasingly peralkaline and progressively enriched only in Si, Rb, Cs, and possibly U with time. They represent successive eruption of the uppermost magma in the postcaldera magma chamber. Eruptive units of La Primavera are either aphyric or contain up to 15% phenocrysts of sodic sanidine ≥ quartz ≫ ferrohedenbergite > fayalite > ilmenite ± titanomagnetite. Major element compositions of sanidine, clinopyroxene, and fayalite phenocrysts vary only slightly between eruptive groups, but the concentrations of many trace elements change by factors of 5-10. This is reflected in phenocryst/glass partition coefficients that differ by factors of up to 20 between successively erupted units. Because the major element compositions of the phenocrysts and the pressure, temperature, and ƒO2 of the magmas were essentially constant, the large variations in partitioning behavior are thought to result from small changes in bulk composition of the melt. Crystal settling and incremental partial melting are by themselves incapable of producing either the chemical gradients within the Tala Tuff magma chamber or the trends with time in the post-95,000-year lavas. Rather, diffusional processes in the silicate liquid are thought to have been the dominant differentiation mechanisms. The zonation in the Tala Tuff is attributed to transport of trace metals as volatile complexes within a thermal and gravitational gradient in a volatile-rich but water-undersaturated magma. The evolution of the postcaldera lavas with time is thought to involve the diffusive emigration of trace elements from a relatively dry magma as a decreasing proportion of network modifiers and/or a decreasing concentration of complexing ligands progressively reduced octahedral site availability in the silicate melt.

Paleomagnetism of the Oligocene Kalamazoo Tuff: implications for middle Tertiary extension in east central Nevada

USGS Publications Warehouse

Hagstrum, J.T.; Gans, P.B.

1989-01-01

The Oligocene Kalamazoo Tuff (???35 Ma) was sampled for paleomagnetic analysis across a 100-km-wide zone of highly extended crust in east central Nevada to estimate between-site vertical axis rotations and thus the relative importance of strike-slip faulting to the mechanism of extension. The tilt-corrected data, with sources of error reduced or eliminated, exhibit a 28?? ?? 12?? clockwise rotation of the Schell Creek Range relative to the Kern Mountains region. This rotation implies differential extension accommodated by strike-slip faulting or N-S shortening. The paleomagnetic results also suggest that large changes in strike of layered units near faults with presumed strike-slip movement need not be the result of oroclinal bending, but could result from superimposed sets of orthogonal normal faults. -from Authors

Mechanistic insights into aqueous phase propanol dehydration in H-ZSM-5 zeolite

DOE Office of Scientific and Technical Information (OSTI.GOV)

Mei, Donghai; Lercher, Johannes A.

Aqueous phase dehydration of 1-propanol over H-ZSM-5 zeolite was investigated using density functional theory (DFT) calculations. The water molecules in the zeolite pores prefer to aggregate via the hydrogen bonding network and be protonated at the Brønsted acidic sites (BAS). Two typical configurations, i.e., dispersed and clustered, of water molecules were identified by ab initio molecular dynamics simulation of the mimicking aqueous phase H-ZSM-5 zeolite unit cell with 20 water molecules per unit cell. DFT calculated Gibbs free energies suggest that the dimeric propanol-propanol, the propanol-water complex, and the trimeric propanol-propanol-water are formed at high propanol concentrations, which provide amore » kinetically feasible dehydration reaction channel of 1-propanol to propene. However, calculation results also indicate that the propanol dehydration via the unimolecular mechanism becomes kinetically discouraged due to the enhanced stability of the protonated dimeric propanol and the protonated water cluster acting as the BAS site for alcohol dehydration reaction. This work was supported by the US Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences & Biosciences. Pacific Northwest National Laboratory (PNNL) is a multiprogram national laboratory operated for DOE by Battelle. Computing time was granted by the grand challenge of computational catalysis of the William R. Wiley Environmental Molecular Sciences Laboratory (EMSL). EMSL is a national scientific user facility located at Pacific Northwest National Laboratory (PNNL) and sponsored by DOE’s Office of Biological and Environmental Research.« less

Geologic Reconnaissance of the Antelope-Ashwood Area, North-Central Oregon: With Emphasis on the John Day Formation of Late Oligocene and Early Miocene Age

USGS Publications Warehouse

Peck, Dallas L.

1964-01-01

This report briefly describes the geology of an area of about 750 square miles in Jefferson, Wasco, Crook, and Wheeler Counties, Oregon. About 16,000 feet of strata that range in age from pre-Tertiary to Quaternary are exposed. These include the following units: pre-Tertiary slate, graywacke, conglomerate, and meta-andesite; Clarno Formation of Eocene age - lava flows, volcanic breccia, tuff, and tuffaceous mudstone, chiefly of andesitic composition; John Day Formation of late Oligocene and early Miocene age - pyroclastic rocks, flows, and domes, chiefly of rhyolitic composition; Columbia River Basalt of middle Miocene age - thick, columnar jointed flows of very fine grained dense dark-gray basalt; Dalles Formation of Pliocene age - bedded tuffaceous sandstone, siltstone, and conglomerate; basalt of Pliocene or Pleistocene age - lava flows of porous-textured olivine basalt; and Quaternary loess, landslide debris, and alluvium. Unconformities separate pre-Tertiary rocks and Clarno Formation, Clarno and John Day Formations, John Day Formation and Columbia River Basalt, and Columbia River Basalt and Dalles Formation. The John Day Formation, the only unit studied in detail, consists of about 4,000 feet of tuff, lapilli tuff, strongly to weakly welded rhyolite ash flows, and less abundant trachyandesite flows and rhyolite flows and domes. The formation was divided into nine mappable members in part of the area, primarily on the basis of distinctive ledge-forming welded ash-flow sheets. Most of the sheets are composed of stony rhyolite containing abundant lithophysae and sparse phenocrysts. One sheet contains 10 to 20 percent phenocrysts, mostly cryptoperthitic soda sanidine, but including less abundant quartz, myrmekitic intergrowths of quartz and sanidine, and oligoclase. The rhyolitic ash flows and lava flows were extruded from nearby vents, in contrast to some of the interbedded air-fall tuff and lapilli tuff of dacitic and andesitic composition that may have been derived from vents in an ancestral Cascade Range. The John Day is dated on the basis of a late Oligocene flora near the base of the formation and early Miocene faunas near the top of the formation. The middle Miocene and older rocks in the Antelope-Ashwood area are broadly folded and broken along northeast-trending faults. Over much of the area the rocks dip gently eastward from the crest of a major fold and are broken along a series of steeply dipping antithetic strike faults. Pliocene and Quaternary strata appear to be undeformed. At the Priday agate deposit, chalcedony-filled spherulites (thunder-eggs) occur in the lower part of a weakly welded rhyolitic ash flow. The so-called thunder-eggs are small spheroidal bodies, about 3 inches in average diameter; each consists of a chalcedonic core surrounded by a shell of welded tuff that is altered to radially oriented fibers of cristobalite and alkalic feldspar.

Microgravity

NASA Image and Video Library

1995-10-20

Onboard Space Shuttle Columbia (STS-73) Payload Specialist Albert Sacco loads autoclaves using a power screwdriver into the Zeolite Crystal Growth (ZCG) experiment in the middeck for the United States Microgravity Laboratory 2 (USML-2) Spacelab mission.

Eruptive and noneruptive calderas, northeastern San Juan Mountains, Colorado: Where did the ignimbrites come from?

USGS Publications Warehouse

Lipman, P.W.; McIntosh, W.C.

2008-01-01

The northeastern San Juan Mountains, the least studied portion of this well-known segment of the Southern Rocky Mountains Volcanic Field are the site of several newly identified and reinterpreted ignimbrite calderas. These calderas document some unique eruptive features not described before from large volcanic systems elsewhere, as based on recent mapping, petrologic data, and a large array of newly determined high-precision, laser-fusion 40Ar/39Ar ages (140 samples). Tightly grouped sanidine ages document exceptionally brief durations of 50-100 k.y. or less for individual Oligocene caldera cycles; biotite ages are more variable and commonly as much as several hundred k.y. older than sanidine from the same volcanic unit. A previously unknown ignimbrite caldera at North Pass, along the Continental Divide in the Cochetopa Hills, was the source of the newly distinguished 32.25-Ma Saguache Creek Tuff (???400-500 km3). This regionally, distinctive crystal-poor alkalic rhyolite helps fill an apparent gap in the southwestward migration from older explosive activity, from calderas along the N-S Sawatch locus in central Colorado (youngest, Bonanza Tuff at 33.2 Ma), to the culmination of Tertiary volcanism in the San Juan region, where large-volume ignimbrite eruptions started at ca. 29.5 Ma and peaked with the enormous Fish Canyon Tuff (5000 km3) at 28.0 Ma. The entire North Pass cycle, including caldera-forming Saguache Creek Tuff, thick caldera-filling lavas, and a smaller volume late tuff sheet, is tightly bracketed at 32.25-32.17 Ma. No large ignimbrites were erupted in the interval 32-29 Ma, but a previously unmapped cluster of dacite-rhyolite lava flows and small tuffs, areally associated with a newly recognized intermediate-composition intrusion 5 ?? 10 km across (largest subvolcanic intrusion in San Juan region) centered 15 km north of the North Pass caldera, marks a near-caldera-size silicic system active at 29.8 Ma. In contrast to the completely filled North Pass caldera that has little surviving topographic expression, no voluminous tuffs vented directly from the adjacent Cochetopa Park caldera, which is morphologically beautifully preserved. Instead, Cochetopa Park subsided passively as the >500 km3 Nelson Mountain Tuff vented at 26.9 Ma from an "underfit" caldera (youngest of the San Luis complex) 30 km to the SW. Three separate regional ignimbrites were erupted sequentially from San Luis calderas within an interval of less than 50-100 k.y., a more rapid recurrence rate for large explosive eruptions than previously documented elsewhere. In eruptive processes, volcanic compositions, areal extent, duration of activity, and magmatic production rates and volumes, the Southern Rocky Mountains Volcanic Field represents present-day erosional remnants of a composite volcanic field, comparable to younger ignimbrite terranes of the Central Andes. ?? 2008 Geological Society of America.

Mechanics of brittle deformation and slope failure at the North Menan Butte tuff cone, Eastern Snake River Plain, Idaho

NASA Astrophysics Data System (ADS)

Okubo, C. H.

2013-12-01

The Menan Volcanic Complex consists of phreatomagmatic tuff cones that were emplaced as part of the regional volcanic activity in the Snake River Plain during the late Pleistocene. These tuff cones, the ';Menan Buttes', resulted from the eruption of basaltic magma through water-saturated alluvium and older basalts along the Snake River. The tuffs are composed primarily of basaltic glass with occasional plagioclase and olivine phenocrysts. The tuff is hydrothermally altered to a massive palagonitic tuff at depth but is otherwise poorly welded. Mass movements along the flanks of the cones were contemporaneous with tuff deposition. These slope failures are manifest as cm- to meter-scale pure folds, faults and fault-related folds, as well as larger slumps that are tens to a few hundred meters wide. Previous investigations classified the structural discontinuities at North Menan Butte based on orientation and sense of displacement, and all were recognized as opening-mode or shear fractures (Russell and Brisbin, 1990). This earlier work also used a generalized model of static (i.e., aseismic) gravity-driven shear failure within cohesionless soils to infer a possible origin for these fractures through slope failure. Recent work at North Menan Butte has provided novel insight into the styles of brittle deformation present, the effect of this deformation on the circulation of subsurface fluids within the tuff cone, as well as the mechanisms of the observed slope failures. Field observations reveal that the brittle deformation, previously classified as fractures, is manifest as deformation bands within the non-altered, poorly welded portions of the tuff. Both dilational and compactional bands, with shear, are observed. Slumps are bounded by normal faults, which are found to have developed within clusters of deformation bands. Deformation bands along the down-slope ends of these failure surfaces are predominantly compactional in nature. These bands have a ~3800 millidarcy permeability, a decrease from the ~9400 millidarcy permeability typical of the non-deformed, poorly-welded tuff. As such, these bands would have acted to slow to the circulation of local fluids through the tuff cone, possibly reducing the slopes' stability further. Future work will employ slope stability models to investigate the tendency for slumping of these tuffs shortly after their emplacement, accounting for water-saturated conditions and the effects of eruption-related seismicity. These results will improve current understanding of the mechanics of fault growth within basaltic tuff and enable more rigorous assessments of the hazards posed by slope instability on active phreatomagmatic tuff cones.

Tephra layers of blind Spring Valley and related upper pliocene and pleistocene tephra layers, California, Nevada, and Utah: isotopic ages, correlation, and magnetostratigraphy

USGS Publications Warehouse

Sarna-Wojcicki, Andrei M.; Reheis, Marith C.; Pringle, Malcolm S.; Fleck, Robert J.; Burbank, Doug; Meyer, Charles E.; Slate, Janet L.; Wan, Elmira; Budahn, James R.; Troxel, Bennie; Walker, James P.

2005-01-01

Numerical ages have been determined for a stratigraphic sequence of silicic tephra layers exposed at the Cowan Pumice Mine in Blind Spring Valley, near Benton Hot Springs, east-central California, as well as at Chalk Cliffs, north of Bishop, Calif. The tephra layers at these sites were deposited after eruptions from nearby sources, most of them from near Glass Mountain, and some from unknown sources. The ages were determined primarily by the laser-fusion 40Ar/39Ar method, mostly on sanidine feldspar; two were determined by conventional K-Ar analysis on obsidian clasts. These tephra layers, all underlying the Bishop ash bed and listed in order of concordant age and stratigraphic position, are: Tephra Unit Method Material Age Bishop Tuff (air-fall pumice) Ar/Ar sanidine 0.759?0.002 Ma* Upper tuffs of Glass Mountain Ar/Ar sanidine 0.87?0.02 Ma Upper tuffs of Glass Mountain Ar/Ar sanidine 1.13?0.19 Ma Lower tuffs of Glass Mountain K-Ar obsidian 1.86?0.09 Ma (avg of 2 dates) Ar/Ar sanidine 1.92?0.02 Ma (avg of 2 dates) Tuffs of Blind Spring Valley Ar/Ar sanidine 2.135?0.02 to sanidine 2.219?0.006 Ma (10 dates) Tuffs of Benton Hot Springs Ar/Ar plagioclase 2.81?0.02 Ma *Date published previously The above tephra layers were also petrographically examined and the volcanic glass shards of the layers were chemically analyzed using the electron microprobe and, for some samples, instrumental neutron activation analysis and X-ray fluorescence. The same types of chemical and petrographic analyses were conducted on stratigraphic sequences of tephra layers of suspected upper Pliocene and Pleistocene age in several past and present depositional basins within the region outside of Blind Spring Valley. Chemical characterization, combined with additional dates and with magnetostratigraphy of thick sections at two of the distal sites, allow correlation of the tephra layers at the Cowan Pumice Mine with layers present at the distal sites and provide age constraints for other intercalated tephra layers and sediments for which age data were previously lacking. The identification at several sections of the widespread Huckleberry Ridge ash bed, derived from the Yellowstone eruptive source area in Wyoming, as well as a new 40Ar/39Ar age on this ash bed from a proximal locality, provide additional age constraints to several of the distal sections. The dated or temporally bracketed distal units, in order of concordant age and stratigraphic position, are: Tephra Unit Method Material Age Tephra layers of Glass Mountain (undiff.) P-mag.*; correlation N/A 1.78 , 1.96, 1.96, 2.22, 2.57, <2.89 Ma Tephra layers of Benton Hot Springs Ar/Ar; correlation plagioclase 2.89?0.03 Ma *Magnetostratigraphic polarity determination At the Cowan Pumice Mine, only a partial section of the eruptive record is preserved, but the best materials for laser-fusion 40Ar/39Ar and other isotopic dating methods were obtained. In the more distal Willow Wash and Confidence Hills sections, both persistent depositional basins for most of late Pliocene time, more complete sections of upper Pliocene tephra layers were preserved. In the region of Glass Mountain, the tephra layers that make up each of the mapped and dated pyroclastic units are multiple and complex, but a progressive simplification of the stratigraphy away from the source area was observed for more distal sites in southern and southwestern California and in Utah. This progressive

Geology of the Mid-Miocene Rooster Comb Caldera and Lake Owyhee Volcanic Field, eastern Oregon: Silicic volcanism associated with Grande Ronde flood basalt

NASA Astrophysics Data System (ADS)

Benson, Thomas R.; Mahood, Gail A.

2016-01-01

The Lake Owyhee Volcanic Field (LOVF) of eastern Oregon consists of rhyolitic caldera centers and lava fields contemporaneous with and spatially related to Mid-Miocene Columbia River flood basalt volcanism. Previous studies delineated two calderas in the southeastern part of LOVF near Owyhee Reservoir, the result of eruptions of two ignimbrites, the Tuff of Leslie Gulch and the Tuff of Spring Creek. Our new interpretation is that these two map units are differentially altered parts of a single ignimbrite produced in a major phreatomagmatic eruption at 15.8 Ma. Areas previously mapped as Tuff of Spring Creek are locations where the ignimbrite contains abundant clinoptilolite ± mordenite, which made it susceptible to erosion. The resistant intracaldera Tuff of Leslie Gulch has an alteration assemblage of albite ± quartz, indicative of low-temperature hydrothermal alteration. Our new mapping of caldera lake sediments and pre- and post-caldera rhyolitic lavas and intrusions that are chemically similar to intracaldera Tuff of Leslie Gulch point to a single 20 × 25 km caldera, which we name the Rooster Comb Caldera. Erosion of the resurgently uplifted southern half of the caldera created dramatic exposures of intracaldera Tuff of Leslie Gulch cut by post-caldera rhyolite dikes and intrusions that are the deeper-level equivalents of lava domes and flows that erupted into the caldera lake preserved in exposures to the northeast. The Rooster Comb Caldera has features in common with more southerly Mid-Miocene calderas of the McDermitt Volcanic Field and High Rock Caldera Complex, including formation in a basinal setting shortly after flood basalt eruptions ceased in the region, and forming on eruption of peralkaline ignimbrite. The volcanism at Rooster Comb Caldera postdates the main activity at McDermitt and High Rock, but, like it, begins 300 ky after flood basalt volcanism begins in the area, and while flood basalts don't erupt through the silicic focus, are contemporaneous with the latest stages of eruptions nearby. High Rock and McDermitt rhyolites are associated with propagation of Steens Basalt dikes to the south, and LOVF rhyolites with later propagation of Grande Ronde Basalt dikes to the north and north-northwest.

MX Siting Investigation Geotechnical Evaluation Conterminous United States. Volume II. Intermediate Screening.

DTIC Science & Technology

1977-12-21

sections of the CSP ( Thordarson and others, 1967; Figure 8). Interbedded materials consist of agglomerates, air-fall and ash-flow tuffs which are welded to...of Economic Geology, 1977, Land resource map of Texas: Bur. Econ. Geol., Univ. Texas, Austin, Texas. (in press). Thordarson , W., Young, R.A., and

Geology and ore deposits of the McDermitt Caldera, Nevada-Oregon

USGS Publications Warehouse

Rytuba, James J.

1976-01-01

The McDermitt caldera is a Miocene collapse structure along the Nevada-Oregon border. The oval-shaped caldera is bounded by arcuate normal faults on the north and south and by rhyolite ring domes on the west. Precollapse ash-flow tuffs exposed within the south caldera rim consist of three cooling units and are peralkaline in composition. Refractive indexes of nonhydrated glasses from basal vitrophyres of the. units range from 1.493 to 1.503 and are typical of comendites. Post-collapse intracaldera rocks consist of tuffaceous lake sediments, rhyolite flows and domes, and ash-flow tuffs. Within the caldera are the mercury mines of Bretz, Cordero, McDermitt, Opalite, and Ruja and the Moonlight uranium mine. The mercury mines are adjacent to ring fracture faults, and the uranium mine and other uranium occurrences are located within rhyolite ring domes. Fluid inclusions in quartz indicate a deposition temperature of 340?C for the uranium deposit and 200?C for the mercury deposits. The mercury deposits formed at shallow depth by replacement of lakebed sediments and volcanic rocks.

Hydrovolcanic and Hydrothermal Biomediated Mineral Growth in Basaltic Tuff, Surtsey Volcano, Iceland

NASA Astrophysics Data System (ADS)

Jackson, M. D.; Couper, S.; Ivarsson, M.; Stan, C. V.; Tamura, N.; Miyagi, L. M.; Moore, J. G.

2017-12-01

Fine-scale analyses of hydroclasts in 1979 Surtsey basaltic tuff drill core provide new methods for examining hydrovolcanic and hydrothermal magma-rock influences on biomediated alteration in palagonitized submarine tephra. Synchrotron source X-ray microdiffraction and microfluorescence studies from Advanced Light Source beamline 12.3.2, epifluorescent UVA illumination microscopy, S/TEM EDX compositional analyses, and Raman spectroscopy define diverse nanocrystalline clay mineral structures at 137.9 m depth (93.8 °C (1980)) and 102.6 m depth (141.3 °C (1980)). At 137.9 m, olivine contains endolithic microborings; vermicular microstructures in altered glass contain nontronite exhibiting crystallographic preferred orientation; and 75-150 µm sub-circular microstructures in altered glass contain Al-tobermorite, a calcium-silicate-hydrate with 11.3 Å interlayer spacing, zeolite, and epifluorescent, thread-like structures. At 102.6 m depth, concentrically-layered microstructures occur in altered glass and altered olivine. These have nontronite crystallographic preferred orientations that rotate around a longitudinal axis commonly occupied by a 10-80 µm long, epifluorescent thread-like structure. Pronounced carbon concentrations detected by S/TEM EDX trace layer boundaries. First-order Raman bands at 1370 cm-1 (disorder-related) and at 1580 cm-1 (order-related), and second-order bands at 2500-3300 cm-1 (overtone scattering) detect degraded organic carbonaceous matter, a strong indication of biological origin. Sub-circular nanostructures in altered glass at 137.9 m depth show similar spectra. Borehole fluid temperatures at 102.6 m, 141.3 °C in 1980, exceeded 130 °C, the assumed limit for growth of microorganisms, however. Previous analyses suggest an early low temperature episode in submarine deposits, prior to development of a hydrothermal system driven by 1964-1967 magmatic intrusions. The abundant traces of biomediated nanocrystalline clay mineral growth validate this hypothesis. Hydrovolcanic fragmentation apparently increased ingress of seawater from the marine biosphere. Both eruptive and hydrothermal water-rock interactions influenced palagonitic alteration at the submillimeter scale during diverse temperature chronologies in the very young volcano.

Hydrogeology of rocks penetrated by test well JF-3, Jackass Flats, Nye County, Nevada

DOE Office of Scientific and Technical Information (OSTI.GOV)

Plume, R.W.; La Camera, R.J.

1996-12-31

The U.S. Department of Energy and U.S. Geological Survey are monitoring water levels in southern Nevada and adjacent parts of California in response to concern about the potential effects of pumping ground water to support the Yucca Mountain Site-Characterization Program. Well JF-3 was drilled in the western part of Jackass Flats for monitoring water levels, for determining the likelihood of a hydraulic connection between well JF-3 and production wells J-12 and J-13, and for measuring the hydraulic properties of the Topopah Spring Tuff. The borehole for JF-3 penetrated about 480 feet of alluvium and 818 feet of underlying volcanic rock.more » The well was finished at a depth of 1,138 feet below land surface near the base of the Topopah Spring Tuff, which is the principal volcanic-rock aquifer in the area. The Topopah Spring Tuff at well JF-3 extends from depths of 580 feet to 1,140 feet and consists of about 10 feet of partly to moderately welded ash-flow tuff; 10 feet of vitrophyre; 440 feet of devitrified, moderately to densely welded ash-flow tuff; 80 feet of densely welded ash-flow tuff; 10 feet of vitric, nonwelded to partly welded ash-flow tuff; and 10 feet of ashfall tuff. Fractures and lithophysae are most common in the devitrified tuff, especially between depths of 600 feet and 1,040 feet. Much of the water produced in well JF-3 probably comes from the sequence of these devitrified tuffs that is below the water table. The transmissivity of the aquifer is an estimated 140,000-160,000 feet squared per day and hydraulic conductivity is 330-370 feet per day. These values exceed estimates made at well J-13 by two orders of magnitude. Such large differences may be accounted for by differences in the development of fractures and lithophysae in the Topopah Spring Tuff at the two wells.« less

Triaxial- and uniaxial-compression testing methods developed for extraction of pore water from unsaturated tuff, Yucca Mountain, Nevada

DOE Office of Scientific and Technical Information (OSTI.GOV)

Mower, T.E.; Higgins, J.D.; Yang, I.C.

1989-12-31

To support the study of hydrologic system in the unsaturated zone at Yucca Mountain, Nevada, two extraction methods were examined to obtain representative, uncontaminated pore-water samples from unsaturated tuff. Results indicate that triaxial compression, which uses a standard cell, can remove pore water from nonwelded tuff that has an initial moisture content greater than 11% by weight; uniaxial compression, which uses a specifically fabricated cell, can extract pore water from nonwelded tuff that has an initial moisture content greater than 8% and from welded tuff that has an initial moisture content greater than 6.5%. For the ambient moisture conditions ofmore » Yucca Mountain tuffs, uniaxial compression is the most efficient method of pore-water extraction. 12 refs., 7 figs., 2 tabs.« less

Energy Dissipation in Calico Hills Tuff due to Pore Collapse

NASA Astrophysics Data System (ADS)

Lockner, D. A.; Morrow, C. A.

2008-12-01

Laboratory tests indicate that the weakest portions of the Calico Hills tuff formation are at or near yield stress under in situ conditions and that the energy expended during incremental loading can be more than 90 percent irrecoverable. The Calico Hills tuff underlies the Yucca Mountain waste repository site at a depth of 400 to 500 m within the unsaturated zone. The formation is highly variable in the degree of both vitrification and zeolitization. Since 1980, a number of boreholes penetrated this formation to provide site characterization for the YM repository. In the past, standard strength measurements were conducted on core samples from the drillholes. However, a significant sampling bias occurred in that tests were preferentially conducted on highly vitrified, higher-strength samples. In fact, the most recent holes were drilled with a dry coring technique that would pulverize the weakest layers, leaving none of this material for testing. We have re-examined Calico Hills samples preserved at the YM Core Facility and selected the least vitrified examples (some cores exceeded 50 percent porosity) for mechanical testing. Three basic tests were performed: (i) hydrostatic crushing tests (to 350 MPa), (ii) standard triaxial deformation tests at constant effective confining pressure (to 70 MPa), and (iii) plane strain tests with initial conditions similar to in situ stresses. In all cases, constant pore pressure of 10 MPa was maintained using argon gas as a pore fluid and pore volume loss was monitored during deformation. The strongest samples typically failed along discrete fractures in agreement with standard Mohr-Coulomb failure. The weaker, high porosity samples, however, would fail by pure pore collapse or by a combined shear-induced compaction mechanism similar to failure mechanisms described for porous sandstones and carbonates. In the plane-strain experiments, energy dissipation due to pore collapse was determined for eventual input into dynamic wave calculations. These calculations will simulate ground accelerations at the YM repository due to propagation of high-amplitude compressional waves generated by scenario earthquakes. As an example, in one typical test on a sample with 43 percent starting porosity, an axial stress increase of 25 MPa resulted from 6 percent shortening and energy dissipation (due to grain crushing and pore collapse) of approximately 1.5x106 J/m3. Under proper conditions, this dissipation mechanism could represent a significant absorption of radiated seismic energy and the possible shielding of the repository from extreme ground shaking.

Geology of the Western Part of Los Alamos National Laboratory (TA-3 to TA-16), Rio Grande Rift, New Mexico

DOE Office of Scientific and Technical Information (OSTI.GOV)

C.J.Lewis; A.Lavine; S.L.Reneau

2002-12-01

We present data that elucidate the stratigraphy, geomorphology, and structure in the western part of Los Alamos National Laboratory between Technical Areas 3 and 16 (TA-3 and TA-16). Data include those gathered by geologic mapping of surficial, post-Bandelier Tuff strata, conventional and high-precision geologic mapping and geochemical analysis of cooling units within the Bandelier Tuff, logging of boreholes and a gas pipeline trench, and structural analysis using profiles, cross sections, structure contour maps, and stereographic projections. This work contributes to an improved understanding of the paleoseismic and geomorphic history of the area, which will aid in future seismic hazard evaluationsmore » and other investigations. The study area lies at the base of the main, 120-m (400-ft) high escarpment formed by the Pajarito fault, an active fault of the Rio Grande rift that bounds Los Alamos National Laboratory on the west. Subsidiary fracturing, faulting, and folding associated with the Pajarito fault zone extends at least 1,500 m (5,000 ft) to the east of the main Pajarito fault escarpment. Stratigraphic units in the study area include upper units of the Tshirege Member of the early Pleistocene Bandelier Tuff, early Pleistocene alluvial fan deposits that predate incision of canyons on this part of the Pajarito Plateau, and younger Pleistocene and Holocene alluvium and colluvium that postdate drainage incision. We discriminate four sets of structures in the area between TA-3 and TA-16: (a) north-striking faults and folds that mark the main zone of deformation, including a graben in the central part of the study area; (b) north-northwest-striking fractures and rare faults that bound the eastern side of the principal zone of deformation and may be the surface expression of deep-seated faulting; (c) rare northeast-striking structures near the northern limit of the area associated with the southern end of the Rendija Canyon fault; and (d) several small east-west-striking faults. We consider all structures to be Quaternary in that they postdate the Tshirege Member (1.22 million years old) of the Bandelier Tuff. Older mesa-top alluvial deposits (Qoal), which may have a large age range but are probably in part about 1.13 million years old, are clearly faulted or deformed by many structures. At two localities, younger alluvial units (Qfo and Qfi) appear to be truncated by faults, but field relations are obscure, and we cannot confirm the presence of fault contacts. The youngest known faulting in the study area occurred in Holocene time on a down-to-the-west fault, recently trenched at the site of a new LANL Emergency Operations Center (Reneau et al. 2002).« less

Synchrotron Powder X-ray Diffraction Study of the Structure and Dehydration Behavior of Sepiolite

DOE Office of Scientific and Technical Information (OSTI.GOV)

Post,J.; Bish, D.; Heaney, P.

2007-01-01

Rietveld refinements using synchrotron powder X-ray diffraction data were used to study the crystal structure and dehydration behavior of sepiolite from Durango, Mexico. The room-temperature (RT) sepiolite structure in air compares well with previous models but reveals an additional zeolitic H{sub 2}O site. The RT structure under vacuum retained only {approx}1/8 of the zeolitic H{sub 2}O and the volume decreased by 1.3%. Real-time, temperature-resolved synchrotron powder X-ray diffraction data and Rietveld refinements were used to investigate the behavior of the sepiolite structure from 300 to 925 K. Rietveld refinements revealed that most of the zeolitic H{sub 2}O is lost bymore » {approx}390 K, accompanied by a decrease in the a and c unit-cell parameters. Above {approx}600 K the sepiolite structure folds as one-half of the crystallographically bound H{sub 2}O is lost. Rietveld refinements of the 'anhydrous' sepiolite structure reveal that, in general, unit-cell parameters a and b and volume steadily decrease with increasing temperature; there is an obvious change in slope at {approx}820 K suggesting a phase transformation coinciding with the loss of the remaining bound H{sub 2}O molecule.« less

Preliminary evaluation of the landsat-4 thematic mapper data for mineral exploration

USGS Publications Warehouse

Podwysocki, M.H.; Power, M.S.; Jones, O.D.

1985-01-01

Landsat-4 Thematic Mapper (TM) data recorded over an arid terrain were analyzed to determine the applicability of using of TM data for identifying and mapping hydrothermally altered, potentially mineralized rocks. Clays, micas, and other minerals bearing the OH anion in specific crystal lattice positions have absorption bands in the 2.2-??m region (TM channel 7, TM7) and commonly lack features in the 1.6-??m region (TM5). Channel ratios TM5/TM7, TM5/TM4, and TM3/TM1 were combined into a color-ratio-composite (CRC) image and used to distinguish hydrothermally altered rocks, unaltered rocks, and vegetation. These distinctions are made possible by using the TM5 and TM7, channels which are not available in the Landsat multispectral scanner (MSS). Digital masking was used to eliminate ambiguities due to water and shadows. However, some ambiguities in identification resulted between altered volcanic rocks and unaltered sedimentary deposits that contained clays, carbonates, and gypsum, and between altered volcanic rocks and volcanic tuffs diagenetically altered to zeolites. However, compared to MSS data, TM data should greatly improve the ability to map hydrothermally altered rocks in arid terrains. ?? 1985.

Geotechnical Assessment of United States and Foreign Test Sites and Material Properties of Geologic Media

DTIC Science & Technology

1979-06-01

kilometers. Hydraulic fracturing data in crystalline rock and indicates that the stress state-varies depending on the tectonic environment (Figure 17). The...S. CAROLINA 0 -A GRANITE. WISCONSIN SO 10 * GRANITE. CALIFORNIA 0 NTS TUFF. NEVADA A 10 t0 50 40 Figure 17. Hydraulic fracturing data in Crystalline

Investigations on Local Seismic Phases and Modeling of Seismic Signals

DTIC Science & Technology

1993-10-31

basement is 1 km. The water table, wt , is from Doty and Thordarson (1983). It separates the dry, DT, and the wet, WT, tuff levels. Above these volcanic...regional variations of t*(f) in the United States. Geophys. J. R. astr. Soc. 82 , 125-140 Doty, G. C. and W. Thordarson , 1983. Water table in rocks of

Deformation of the Wineglass Welded Tuff and the timing of caldera collapse at Crater Lake, Oregon

USGS Publications Warehouse

Kamata, H.; Suzuki-Kamata, K.; Bacon, C.R.

1993-01-01

Four types of deformation occur in the Wineglass Welded Tuff on the northeast caldera rim of Crater Lake: (a) vertical tension fractures; (b) ooze-outs of fiamme: (c) squeeze-outs of fiamme; and (d) horizontal pull-apart structures. The three types of plastic deformation (b-d) developed in the lower part of the Wineglass Welded Tuff where degree of welding and density are maximum. Deformation originated from concentric normal faulting and landsliding as the caldera collapsed. The degree of deformation of the Wineglass Welded Tuff increases toward the northeast part of the caldera, where plastic deformation occurred more easily because of a higher emplacement temperature probably due to proximity to the vent. The probable glass transition temperature of the Wineglass Welded Tuff suggests that its emplacement temperature was ???750??C where the tuff is densely welded. Calculation of the conductive cooling history of the Wineglass Welded Tuff and the preclimactic Cleetwood (lava) flow under assumptions of a initially isothermal sheet and uniform properties suggests that (a) caldera collapse occurred a maximum of 9 days after emplacement of the Wineglass Welded Tuff, and that (b) the period between effusion of the Cleetwood (lava) flow and onset of the climactic eruption was <100 years. If cooling is controlled more by precipitation during quiescent periods than by conduction, these intervals must be shorter than the calculated times. ?? 1993.

Petrochemistry of late miocene peraluminous silicic volcanic rocks from the Morococala field, Bolivia

USGS Publications Warehouse

Morgan, VI G.B.; London, D.; Luedke, R.G.

1998-01-01

Late Miocene peraluminous volcanic rocks of the Morococala field, Bolivia, define a layered stratigraphy of basal andalusite-, biotite-(?? Muscovite)-bearing rhyolite tuffs (AR), overlain by cordierite-, biotite-bearing rhyolite tuffs (CR), and capped by biotite-beanng quartz latite tuffs, lavas, and late domal flows (QL). Mineral and whole-rock compositions become more evolved from top to bottom, with differentiation reflected by decreasing Ca, Ba, Mg, Fe, and rare earth elements (REE) versus increasing F, Na/K, and aluminosity from QL to AR. Mineral, whole-rock, and glass inclusion compositions are consistent with derivation of all three rock types from a single stratified magma reservoir, but age and spatial relations between the three units make this unlikely. Genesis of the QL involved biotite-dehydration melting of an aluminous source at T > 750??C and P ??? 4-6 kbar. If not co-magmatic with QL, the other units were generated primarily by muscovite-dehydration melting at T = 730-750??C and P ??? 3??5-4??5 kbar for CR, and T ??? 750??C for AR with pre-emptive residence at low pressure (1??5-3??0 kbar). Low hematite contents (XHem ??? 0??06) of ilmenite grains in AR, CR, and early grains (as inclusions in plagioclase and sanidine cores) in QL indicate reduced conditions imposed by a graphite-bearing source. Compositional variability among texturally later oxides (ilmenite with XHem = 0??06-0??50, primary magnetite), however, apparently records progressive increases in pre-eruptive f(O2) in QL. Plagioclase-melt equilibria and electron microprobe analysis difference for quartz-hosted glass inclusions suggest pre-emptive melt H2O contents ??? 5-7 wt % for the AR, ???4-6 wt % for the CR, and ???3-5 wt % for the QL.

The Bossoroca Complex, São Gabriel Terrane, Dom Feliciano Belt, southernmost Brazil: Usbnd Pb geochronology and tectonic implications for the neoproterozoic São Gabriel Arc

NASA Astrophysics Data System (ADS)

Gubert, Mauricio Lemos; Philipp, Ruy Paulo; Stipp Basei, Miguel Angelo

2016-10-01

Usbnd Pb LA-ICPMS geochronological analyses were carried out on zircon grains from metavolcanic rocks of the Bossoroca Complex and for one ash tuff of the Acampamento Velho Formation of the Camaquã Basin, in order to understand the evolution of the Neoproterozoic São Gabriel magmatic arc. A total of 42 analyses of igneous zircon grains were performed in three samples. The results yielded Usbnd Pb ages of 767.2 ± 2.9 Ma for the metavolcanic agglomerate (BOS-02); 765 ± 10 Ma for the metacrystal tuff (BOS-03) and 565.8 ± 4.8 Ma for the ash tuff (BOS-04). The Orogenic Cycle in Brazil is characterized by a set of orogenic belts consisting of petrotectonic associations juxtaposed by two collisional events that occurred at the end of the Neoproterozoic. In southern Brazil this orogeny formed the Dom Feliciano Belt, a unit composed of associations of rocks developed during two major orogenic events called São Gabriel (900-680 Ma) and Dom Feliciano (650-540 Ma). The main São Gabriel associations are tectonically juxtaposed as elongated strips according to the N20-30°E direction, bounded by ductile shear zones. The Bossoroca Complex comprises predominantly metavolcano-sedimentary rocks, characterized by medium-K calc-alkaline association generated in a cordillera-type magmatic arc. The volcanism occurred in sub-aerial environment, developing deposits generated by flow, resurgence and fall, sporadically interrupted by subaqueous epiclastic deposits, suggesting an arc related basin. The São Gabriel Terrane contains the petrotectonic units that represent the closure of the Charrua Ocean associated to the subduction period of the Brasiliano Orogenic Cycle in the Sul-rio-grandense Shield.

Genesis of the post-caldera eastern Upper Basin Member rhyolites, Yellowstone, WY: from volcanic stratigraphy, geochemistry, and radiogenic isotope modeling

NASA Astrophysics Data System (ADS)

Pritchard, Chad J.; Larson, Peter B.

2012-08-01

An array of samples from the eastern Upper Basin Member of the Plateau Rhyolite (EUBM) in the Yellowstone Plateau, Wyoming, were collected and analyzed to evaluate styles of deposition, geochemical variation, and plausible sources for low δ18O rhyolites. Similar depositional styles and geochemistry suggest that the Tuff of Sulphur Creek and Tuff of Uncle Tom's Trail were both deposited from pyroclastic density currents and are most likely part of the same unit. The middle unit of the EUBM, the Canyon flow, may be composed of multiple flows based on a wide range of Pb isotopic ratios (e.g., 206Pb/204Pb ranges from 17.54 to 17.86). The youngest EUBM, the Dunraven Road flow, appears to be a ring fracture dome and contains isotopic ratios and sparse phenocrysts that are similar to extra-caldera rhyolites of the younger Roaring Mountain Member. Petrologic textures, more radiogenic 87Sr/86Sr in plagioclase phenocrysts (0.7134-0.7185) than groundmass and whole-rock ratios (0.7099-0.7161), and δ18O depletions on the order of 5‰ found in the Tuff of Sulphur Creek and Canyon flow indicate at least a two-stage petrogenesis involving an initial source rock formed by assimilation and fractional crystallization processes, which cooled and was hydrothermally altered. The source rock was then lowered to melting depth by caldera collapse and remelted and erupted. The presence of a low δ18O extra-caldera rhyolite indicates that country rock may have been hydrothermally altered at depth and then assimilated to form the Dunraven Road flow.

Encapsulating Metal Clusters and Acid Sites within Small Voids: Synthetic Strategies and Catalytic Consequences

NASA Astrophysics Data System (ADS)

Goel, Sarika

The selective encapsulation of metal clusters within zeolites can be used to prepare clusters that are uniform in diameter and to protect them against sintering and contact with feed impurities, while concurrently allowing active sites to select reactants based on their molecular size, thus conferring enzyme-like specificity to chemical catalysis. The apertures in small and medium-pore zeolites preclude the use of post-synthetic protocols to encapsulate the relevant metal precursors because cationic or anionic precursors with their charge-balancing double layer and gaseous complexes cannot diffuse through their windows or channels. We have developed general strategies to encapsulate metal clusters within small-pore zeolites by using metal precursors stabilized by ammonia or organic amine ligands, which stabilize metal precursors against their premature precipitation at the high temperature and pH conditions required for the hydrothermal synthesis of the target zeolite structures and favor interactions between metal precursors and incipient aluminosilicate nuclei during the self-assembly of microporous frameworks. When synthesis temperatures were higher than 400 K, available ligands were unable to prevent the premature precipitation of the metal precursors. In such cases, encapsulation was achieved instead via interzeolite transformations after successfully encapsulating metal precursors or clusters via post-synthesis exchange or ligand protection into parent zeolites and subsequently converting them into the target structures while retaining the encapsulated clusters or precursors. Such strategies led to the successful selective encapsulation of a wide range of metal clusters (Pt, Pd, Ru, Rh, Ir, Re, and Ag) within small-pore (SOD (sodalite), LTA (Linde type A (zeolite A)), GIS (gismondine), and ANA (analcime)) and medium-pore (MFI (ZSM-5)) zeolites. These protocols provide novel and diverse mechanism-based strategies for the design of catalysts with protected active sites. We have demonstrated the selectivity of the encapsulation processes by combining transmission electron microscopy and chemisorptive titrations with rigorous catalytic assessments of the ability of these materials to catalyze reactions of small molecules, which can access the intracrystalline voids, but not of larger molecules that cannot access the metal clusters within such voids. The selective confinement of clusters also prevented their contact with sulfur compounds (e.g., thiophene and H2S), thus allowing reactions to occur at conditions that otherwise render unconfined clusters unreactive. We have also developed synthetic protocols and guiding principles, inspired by mechanistic considerations, for the synthesis of zeolites via interzeolite transformations without the use of organic structure-directing agents (OSDA). More specifically, we have synthesized high-silica MFI (ZSM-5), CHA (chabazite), STF (SSZ-35) and MTW (ZSM-12) zeolites from FAU (faujasite) or BEA (beta) parent materials. Structures with lower framework densities (FAU or BEA) were successfully transformed into thermodynamically-favored, more stable structures with higher framework densities (MFI, CHA, STF, and MTW); to date, target materials with higher Si/Al ratios (Si/Al >10) have not been synthesized via interzeolite transformations without the aid of the OSDA species used to discover these zeolite structures and deemed essential up until now for their successful synthesis. Overcoming kinetic hurdles in such transformations required either the presence of common composite building units (CBU) between parent and target structures or, in their absence, the introduction of small amount of seeds of the daughter structures. The NaOH/SiO2 ratio, H2O/SiO2 ratio and Al content in reagents are used to enforce synchronization between the swelling and local restructuring within parent zeolite domains with the spalling of fragments or building units from seeds of the target structure. The pseudomorphic nature of these seed-mediated transformations, which conserve the volume occupied by the parent crystals and lead to similar size and crystal shape in products, reflect incipient nucleation of target structures occurring at the outer regions of the parent domains and lead to the formation of mesoporosity as a natural consequence of the space-conserving nature of these structural changes and of the higher density of the daughter frameworks. The synthesis mechanism and the guidelines developed enable us to enforce conditions required for the formation of zeolites that previously required OSDA species for their synthesis, thus expanding to a significant extent the diversity of zeolite frameworks that are accessible via these synthesis protocols and providing potential savings in the time and cost involved in the synthesis of some of these zeolite structures.

Tephrochronology of Bed II, Olduvai Gorge, Tanzania, and placement of the Oldowan-Acheulean transition.

PubMed

McHenry, Lindsay J; Stanistreet, Ian G

2018-04-12

Tuffaceous marker beds, derived from volcanic products from the Ngorongoro Volcanic Highlands, help define a stratigraphic framework for the world-renowned fossil and stone tool record exposed at Olduvai Gorge, Tanzania. However, previous efforts to constrain this tuff record, especially for Olduvai Bed II, have been limited because of erosion, contamination, reworking, and the alteration of volcanic glass under saline-alkaline conditions. This paper applies previously defined geochemical and mineralogical "fingerprints" for several major Bed II marker tuffs, based on glass (where available) and phenocrysts more resistant to alteration (feldspar, hornblende, augite, and titanomagnetite), to tuffs from stratigraphic sections in the Olduvai Junction Area, including previously and recently excavated Acheulean and Oldowan sites (HWK EE (Locality (Loc) 42), EF-HR (Loc 12a), FLK (Loc 45), and MNK (Loc 88)). The Middle Bed II Bird Print Tuff (BPT) is found to be more compositionally variable than previously reported but is still valuable as a stratigraphic marker over short distances. The confirmation of blocks of Tuff IID in conglomerate helps constrain Upper Bed II stratigraphy at sites where in-situ tuffs are absent. This paper also compiles the results of published geochronological research, providing stratigraphic context and updating previously reported dates using a consistent 40 Ar/ 39 Ar reference standard age. The results of this work support the following paleoanthropologically relevant conclusions: 1) the early Acheulean site EF-HR (Loc 12a) is situated above the level of Hay's Tuff IIC, and thus sits in Upper rather than Middle Bed II, (2) the HWK EE (Loc 42) Oldowan site is constrained between Tuff IIA and Tuff IIB, just above the boundary between Lower and Middle Bed II, and 3) the Acheulean site at FLK W most likely lies within the Middle Augitic Sandstone, above Tuff IIB, similar to the placements by Leakey and Hay for the earliest Acheulean at Olduvai. Copyright © 2018 Elsevier Ltd. All rights reserved.

Nd, Sr, and O isotopic variations in metaluminous ash-flow tuffs and related volcanic rocks at the Timber Mountain/Oasis Valley Caldera, Complex, SW Nevada: implications for the origin and evolution of large-volume silicic magma bodies

USGS Publications Warehouse

Farmer, G.L.; Broxton, D.E.; Warren, R.G.; Pickthorn, W.

1991-01-01

Nd, Sr and O isotopic data were obtained from silicic ash-flow tuffs and lavas at the Tertiary age (16-9 Ma) Timber (Mountain/Oasis Valley volcanic center (TMOV) in southern Nevada, to assess models for the origin and evolution of the large-volume silicic magma bodies generated in this region. The large-volume (>900 km3), chemically-zoned, Topopah Spring (TS) and Tiva Canyon (TC) members of the Paintbrush Tuff, and the Rainier Mesa (RM) and Ammonia Tanks (AT) members of the younger Timber Mountain Tuff all have internal Nd and Sr isotopic zonations. In each tuff, high-silica rhyolites have lower initial e{open}Nd values (???1 e{open}Nd unit), higher87Sr/86Sr, and lower Nd and Sr contents, than cocrupted trachytes. The TS, TC, and RM members have similar e{open}Nd values for high-silica rhyolites (-11.7 to -11.2) and trachytes (-10.5 to -10.7), but the younger AT member has a higher e{open}Nd for both compositional types (-10.3 and -9.4). Oxygen isotope data confirm that the TC and AT members were derived from low e{open}Nd magmas. The internal Sr and Nd isotopic variations in each tuff are interpreted to be the result of the incorporation of 20-40% (by mass) wall-rock into magmas that were injected into the upper crust. The low e{open}Nd magmas most likely formed via the incorporation of low ??18O, hydrothermally-altered, wall-rock. Small-volume rhyolite lavas and ash-flow tuffs have similar isotopic characteristics to the large-volume ash-flow tuffs, but lavas erupted from extracaldera vents may have interacted with higher ??18O crustal rocks peripheral to the main magma chamber(s). Andesitic lavas from the 13-14 Ma Wahmonie/Salyer volcanic center southeast of the TMOV have low e{open}Nd (-13.2 to -13.8) and are considered on the basis of textural evidence to be mixtures of basaltic composition magmas and large proportions (70-80%) of anatectic crustal melts. A similar process may have occurred early in the magmatic history of the TMOV. The large-volume rhyolites may represent a mature stage of magmatism after repeated injection of basaltic magmas, crustal melting, and volcanism cleared sufficient space in the upper crust for large magma bodies to accumulate and differentiate. The TMOV rhyolites and 0-10 Ma old basalts that erupted in southern Nevada all have similar Nd and Sr isotopic compositions, which suggests that silicic and mafic magmatism at the TMOV were genetically related. The distinctive isotopic compositions of the AT member may reflect temporal changes in the isotopic compositions of basaltic magmas entering the upper crust, possibly as a result of increasing "basification" of a lower crustal magma source by repeated injection of mantle-derived mafic magmas. ?? 1991 Springer-Verlag.

Removal of paraquat solution onto zeolite material

NASA Astrophysics Data System (ADS)

Sirival, Rujikarn; Patdhanagul, Nopbhasinthu; Preecharram, Sutthidech; Photharin, Somkuan

2018-04-01

The purpose of this research was to study the adsorption of paraquat herbicides onto zeolite Y materials by the batch method. Three adsorbents material: Zeolite-3, Zeolite-10, and Zeolite-100 were Si/Al ratio at 3.58, 8.57 and 154.37, respectively. The factors for adsorption of paraquat as follows, adsorption time, initial concentrations of paraquat, pH and adsorption isotherm were investigated. The results showed that zeolite-10 had higher adsorption capacity than zeolite-3 and zeolite-100. The appropriate conditions for adsorption were 24 h., Zeolite 0.1 g., Initial paraquat concentration 100 ppm at pH 6. The adsorption isotherm was found to correspond with Langmuir Isotherm and the maximum paraquat adsorption is 26.38 mg/g for zeolite-10, 21.41 mg/g and 9.60 mg/g for zeolite-3 and zeolite-100, respectively. The characterization of zeolite material with XRD, XRF and BET. Furthermore, the zeolite materials applied to remove other organic and inorganic wastewater.

Graphite in the Bishop Tuff and its effect on postcaldera oxygen fugacity

USGS Publications Warehouse

Hildreth, Edward; Ryan-Davis, Juliet; Harlow, Benjamin

2017-01-01

Several cubic kilometers of Paleozoic graphite-bearing argillitic country rocks are present as lithic fragments in Bishop Tuff ignimbrite and fallout. The lithics were entrained by the 650 km3 of rhyolite magma that vented during the 5- to 6-day-long, caldera-forming eruption at Long Valley, California. The caldera is floored by a 350 km2 roof plate that collapsed during the eruption and consists in large part of the Paleozoic strata that provided the abundant hornfelsed metapelitic lithic clasts in the tuff. Graphite has been identified by Raman spectroscopy, electron-dispersive spectroscopy, and X-ray diffraction as an irregularly dispersed component in the small fraction of Bishop Tuff pumice that is dark-colored. Carbon concentration has been determined in pumice, lithics, and wall rocks. Values of δ13C range from –21‰ to –29‰ Vienna Peedee Belemnite (VPDB) for pumice, lithics, and argillitic wall rocks, reflecting the biogenic origin of the reduced carbon in oxygen-limited black Paleozoic marine mudrocks. Carbonate contents, measured separately, are negligible in fresh pumice and lithics. Microprobe analyses of titanomagnetite-ilmenite pairs show that oxygen-fugacity values of numerous batches of postcaldera Early Rhyolite (750–640 ka; ~100 km3) are up to one log unit more reduced than those of the temperature–oxygen fugacity (T-fO2) array of the Bishop Tuff (767 ka), despite similar major-element compositions and Fe-Ti–oxide temperature ranges. All of the many batches of Early Rhyolite, which erupted episodically over an interval of ~125,000 years, yield the reduced fO2 values, indicating that reaction with graphite lowered magmatic fO2 after the caldera-forming eruption but before the first eruption of Early Rhyolite. It is inferred that reaction of postcaldera rhyolite magma with the reduced carbon in a great mass of subsided roof rocks lowered its fO2. It is suggested that comparable effects could have attended caldera collapse of other magma chambers hosted in continental sedimentary rocks.

Fission-track dating of pumice from the KBS Tuff, East Rudolf, Kenya

USGS Publications Warehouse

Hurford, A.J.; Gleadow, A.J.W.; Naeser, C.W.

1976-01-01

Fission-track dating of zircon separated from two pumice samples from the KBS Tuff in the Koobi Fora Formation, in Area 131, East Rudolf, Kenya, gives an age of 2.44??0.08 Myr for the eruption of the pumice. This result is compatible with the previously published K-Ar and 40Ar/ 39Ar age spectrum estimate of 2.61??0.26 Myr for the KBS Tuff in Area 105, but differs from the more recently published K-Ar date of 1.82??0.04 Myr for the KBS Tuff in Area 131. This study does not support the suggestion that pumice cobbles of different ages occur in the KBS Tuff. ?? 1976 Nature Publishing Group.

Rapid screening of the antimicrobial efficacy of Ag zeolites.

PubMed

Tosheva, L; Belkhair, S; Gackowski, M; Malic, S; Al-Shanti, N; Verran, J

2017-09-01

A semi-quantitative screening method was used to compare the killing efficacy of Ag zeolites against bacteria and yeast as a function of the zeolite type, crystal size and concentration. The method, which substantially reduced labor, consumables and waste and provided an excellent preliminary screen, was further validated by quantitative plate count experiments. Two pairs of zeolite X and zeolite beta with different sizes (ca. 200nm and 2μm for zeolite X and ca. 250 and 500nm for zeolite beta) were tested against Escherichia coli (E. coli) and Candida albicans (C. albicans) at concentrations in the range 0.05-0.5mgml -1 . Reduction of the zeolite crystal size resulted in a decrease in the killing efficacy against both microorganisms. The semi-quantitative tests allowed convenient optimization of the zeolite concentrations to achieve targeted killing times. Zeolite beta samples showed higher activity compared to zeolite X despite their lower Ag content, which was attributed to the higher concentration of silver released from zeolite beta samples. Cytotoxicity measurements using peripheral blood mononuclear cells (PBMCs) indicated that Ag zeolite X was more toxic than Ag zeolite beta. However, the trends for the dependence of cytotoxicity on zeolite crystal size at different zeolite concentrations were different for the two zeolites and no general conclusions about zeolite cytotoxicity could be drawn from these experiments. This result indicates a complex relationship, requiring the necessity for individual cytotoxicity measurements for all antimicrobial applications based on the use of zeolites. Copyright © 2017 Elsevier B.V. All rights reserved.

Theoretical Study of the Mechanism Behind the para-Selective Nitration of Toluene in Zeolite H-Beta

DOE Office of Scientific and Technical Information (OSTI.GOV)

Andersen, Amity; Govind, Niranjan; Subramanian, Lalitha

Periodic density functional theory calculations were performed to investigate the origin of the favorable para-selective nitration of toluene exhibited by zeolite H-beta with acetyl nitrate nitration agent. Energy calculations were performed for each of the 32 crystallographically unique Bronsted acid sites of a beta polymorph B zeolite unit cell with multiple Bronsted acid sites of comparable stability. However, one particular aluminum T-site with three favorable Bronsted site oxygens embedded in a straight 12-T channel wall provides multiple favorable proton transfer sites. Transition state searches around this aluminum site were performed to determine the barrier to reaction for both para andmore » ortho nitration of toluene. A three-step process was assumed for the nitration of toluene with two organic intermediates: the pi- and sigma-complexes. The rate limiting step is the proton transfer from the sigma-complex to a zeolite Bronsted site. The barrier for this step in ortho nitration is shown to be nearly 2.5 times that in para nitration. This discrepancy appears to be due to steric constraints imposed by the curvature of the large 12-T pore channels of beta and the toluene methyl group in the ortho approach that are not present in the para approach.« less

Development of metal organic fromwork-199 immobilized zeolite foam for adsorption of common indoor VOCs.

PubMed

Saini, Vipin K; Pires, João

2017-05-01

Reticulated foam shaped adsorbents are more efficient for the removal of volatile organic compounds (VOCs), particularly from low VOC-concentration indoor air streams. In this study composite structure of zeolite and metal organic frameworks (MOFs), referred as ZMF, has been fabricated by immobilization of fine MOF-199 powder on foam shaped Zeolite Socony Mobil-5 (ZSM-5) Zeolitic structure, referred as ZF. The ZMF possess a uniform and well-dispersed coating of MOF-199 on the porous framework of ZF. It shows higher surface area, pore volume, and VOCs adsorption capacity, as compared to ZF-structure. Post-fabrication changes in selective adsorption properties of ZMF were studied with three common indoor VOCs (benzene, n-hexane, and cyclohexane), using gravimetric adsorption technique. The adsorption capacity of ZMF with different VOCs follow the order of benzene>n-hexane>cyclohexane. In comparison with MOF-199 and ZF, the composite structure ZMF shows improvement in selectivity for benzene from other two VOCs. Further, improvement in efficiency and stability of prepared ZMF was found to be associated with its high MOF loading capacity and unique morphological and structural properties. The developed composite structure with improved VOCs removal and recyclability could be a promising material for small to limited scale air pollution treatment units. Copyright © 2016. Published by Elsevier B.V.

Pore-water extraction from unsaturated tuff by triaxial and one-dimensional compression methods, Nevada Test Site, Nevada

USGS Publications Warehouse

Mower, Timothy E.; Higgins, Jerry D.; Yang, In C.; Peters, Charles A.

1994-01-01

Study of the hydrologic system at Yucca Mountain, Nevada, requires the extraction of pore-water samples from welded and nonwelded, unsaturated tuffs. Two compression methods (triaxial compression and one-dimensional compression) were examined to develop a repeatable extraction technique and to investigate the effects of the extraction method on the original pore-fluid composition. A commercially available triaxial cell was modified to collect pore water expelled from tuff cores. The triaxial cell applied a maximum axial stress of 193 MPa and a maximum confining stress of 68 MPa. Results obtained from triaxial compression testing indicated that pore-water samples could be obtained from nonwelded tuff cores that had initial moisture contents as small as 13 percent (by weight of dry soil). Injection of nitrogen gas while the test core was held at the maximum axial stress caused expulsion of additional pore water and reduced the required initial moisture content from 13 to 11 percent. Experimental calculations, together with experience gained from testing moderately welded tuff cores, indicated that the triaxial cell used in this study could not apply adequate axial or confining stress to expel pore water from cores of densely welded tuffs. This concern led to the design, fabrication, and testing of a one-dimensional compression cell. The one-dimensional compression cell used in this study was constructed from hardened 4340-alloy and nickel-alloy steels and could apply a maximum axial stress of 552 MPa. The major components of the device include a corpus ring and sample sleeve to confine the sample, a piston and base platen to apply axial load, and drainage plates to transmit expelled water from the test core out of the cell. One-dimensional compression extracted pore water from nonwelded tuff cores that had initial moisture contents as small as 7.6 percent; pore water was expelled from densely welded tuff cores that had initial moisture contents as small as 7.7 percent. Injection of nitrogen gas at the maximum axial stress did not produce additional pore water from nonwelded tuff cores, but was critical to recovery of pore water from densely welded tuff cores. Gas injection reduced the required initial moisture content in welded tuff cores from 7.7 to 6.5 percent. Based on the mechanical ability of a pore-water extraction method to remove water from welded and nonwelded tuff cores, one-dimensional compression is a more effective extraction method than triaxial compression. However, because the effects that one-dimensional compression has on pore-water chemistry are not completely understood, additional testing will be needed to verify that this method is suitable for pore-water extraction from Yucca Mountain tuffs.

Permian U-Pb (CA-TIMS) zircon ages from Australia and China: Constraining the time scale of environmental and biotic change

NASA Astrophysics Data System (ADS)

Denyszyn, S. W.; Mundil, R.; Metcalfe, I.; He, B.

2010-12-01

In eastern Australia, the interconnected Bowen and Sydney Basins are filled with terrestrial sediments of late Paleozoic to early Mesozoic age. These sedimentary units record significant evolutionary events of eastern Gondwana during the time interval between two major mass extinctions (end Middle Permian and Permian-Triassic), and also provide lithological evidence for the Carboniferous-Permian Late Paleozoic Ice Age of southern Pangea, considered to be divisible into up to seven discrete glaciation events in Australia [e.g., 1]. These glaciations are currently assigned ages that indicate that the last of the glaciations predate the end Middle Permian mass extinction at ca. 260 Ma. However, the estimates for the time and durations are largely based on biostratigraphy and lithostratigraphy that, in the absence of robust and precise radioisotopic ages, are unacceptably fragile for providing an accurate high-resolution framework. Interbedded with the sediments are numerous tuff layers that contain zircon, many of which are associated with extensive coal measures in the Sydney and Bowen Basins. Published SHRIMP U-Pb zircon ages [2, 3] have been shown to be less precise and inaccurate when compared to ages applying the CA-TIMS method to the same horizons. Also within the late Middle Permian, the eruption of the Emeishan flood basalts in SW China has been proposed to have caused the end Middle Permian mass extinction [e.g., 4], though a causal link between these events demands a rigorous test that can only be provided by high-resolution geochronology. We present new U-Pb (CA-TIMS) zircon ages on tuff layers from the Sydney and Bowen Basins, with the purpose of generating a timescale for the Upper Permian of Australia to allow correlation with different parts of the world. Initial results, with permil precision, date a tuff layer within the uppermost Bandanna Fm. to ca. 252 Ma, a tuff within the Moranbah Coal Measures to ca. 256 Ma, and a tuff within the Ingelara Fm. to ca. 257 Ma, the latter two units lying stratigraphically below the latest identified glacial deposits. U-Pb (CA-TIMS) results on zircons from the Emeishan flood basalts and related volcanic products confirm the end-Guadalupian age (ca. 260 Ma) of the magmatism, and based on present data, place the Emeishan volcanic event (and its possibly associated mass extinction) within the occurrence of the Late Paleozoic Ice Age. This study’s primary goal is the establishment of a chronostratigraphic framework that would allow the integration of calibrated records from both terrestrial and marine units from different parts of the world in order to constrain the timing and rates of extinctions and recoveries in different locations and physical environments. [1] Fielding et al. (2008), J. Geol Soc. Lon., v. 165, pp. 129-140 [2] Michaelsen et al. (2001), Aus. J. Earth Sci., v. 48, pp. 183-192 [3] Roberts et al. (1996), Aus. J. Earth Sci., v. 43, pp. 401-421 [4] He et al. (2007), EPSL, v. 255, pp. 306-323

Geologic map of Harrat Hutaymah, with petrologic classification and distribution of ultramafic inclusions, Saudi Arabia

USGS Publications Warehouse

Thornber, Carl R.

1990-01-01

This map shows detailed geology of the Quaternary and Tertiary volcanic deposits that comprise Harrat Hutaymah and an updated and generalized compilation of the underlying Proterozoic and Paleozoic basement rocks. Quaternary alluvial cover and details of basement geology (that is, faults, dikes, and other features) are not shown. Volcanic unit descriptions and contact relations are based upon field investigation by the author and on compilation and revision of mapping Kellogg (1984; northern half of area) and Pallister (1984; southern half of area). A single K-Ar date of 1.80 ± 0.05 Ma for an alkali olivine basalt flow transected by the Al Hutaymah tuff ring (Pallister, 1984) provides the basis for an estimated late Tertiary to Quaternary age range for all harrat volcanic units other than unit Qtr (tuff reworked during Quaternary age time). Contact relations and unit descriptions for the basement rocks were compiled from Pallister (1984), Kellogg (1984 and 1985), DuBray (1984), Johnson and Williams (1984), Vaslet and others (1987), Cole and Hedge (1986), and Richter and others (1984). All rock unit names in this report are informal and capitalization follows Saudi Arabian stratigraphic nomenclature (Fitch, 1980). Geographic information was compiled from Pallister (1984), Kellogg (1984), and Fuller (in Johnson and Williams, 1984) and from field investigation by the author in 1986. The pie diagrams on the map show the distribution and petrology of ultramafic xenoliths of Harrat Hutaymah. The pie diagrams are explained by a detailed classification of ultramafic xenoliths that is introduced in this report.

Influences of Sedimentary Environments and Volcanic Sources on Diagenetic Alteration of Volcanic Tuffs in South China.

PubMed

Gong, Nina; Hong, Hanlie; Huff, Warren D; Fang, Qian; Bae, Christopher J; Wang, Chaowen; Yin, Ke; Chen, Shuling

2018-05-16

Permian-Triassic (P-Tr) altered volcanic ashes (tuffs) are widely distributed within the P-Tr boundary successions in South China. Volcanic altered ashes from terrestrial section-Chahe (CH) and marine section-Shangsi (SS) are selected to further understand the influence of sedimentary environments and volcanic sources on diagenetic alterarion on volcanic tuffs. The zircon 206 Pb/ 238 U ages of the corresponding beds between two sections are almost synchronous. Sedimentary environment of the altered tuffs was characterized by a low pH and did not experience a hydrothermal process. The dominant clay minerals of all the tuff beds are illite-smectite (I-S) minerals, with minor chlorite and kaolinite. I-S minerals of CH (R3) are more ordered than SS (R1), suggesting that CH also shows a higher diagenetic grade and more intensive chemical weathering. Besides, the nature of the volcanism of the tuff beds studied is derived from different magma sources. The clay mineral compositions of tuffs have little relation with the types of source volcanism and the depositional environments. Instead, the degree of the mixed-layer clay minerals and the REE distribution are mainly dependent upon the sedimentary environments. Thus, the mixed-layer clay minerals ratio and their geochemical index can be used as the paleoenvironmental indicator.

Trace and rare-earth element characteristics of acidic tuffs from southern Peru and northern Bolivia and a fission-track age for the sillar of Arequipa

NASA Astrophysics Data System (ADS)

Vatin-Perignon, N.; Poupeau, G.; Oliver, R. A.; La Venu, A.; Labrin, F.; Keller, F.; Bellot-Gurlet, L.

1996-03-01

Trace-element and REE data of glass and pumices of acidic tuffs and related fall deposits erupted in southern Peru and northern Bolivia between 20 and 0.36 Ma display typical characteristics of subduction related continental arc magmatism of the CVZ with strong LILE/HFSE enrichment and non enrichment of HREE and Y. Geochemical variations of these tuffs are linked to subduction processes and controlled by changes in tectonic regimes which occured with each Quechua tectonic pulse and affected the astenospheric wedge and both the dowgoing and the overriding lithospheres. During Neogene — Pleistocene times, tuffs erupted in northern Bolivia are typically enriched in Zr, Hf, Th, Ba, LREEs and other incompatible elements and incompatible /Yb ratios are much higher relative to those erupted from southern Peru, at a given SiO 2 content (65-67 wt. for dacites, 72-73 wt.% for rhyolites). {Zr}/{Hf} ratios increase eastward from 27 to 30 and {Ce}/{Yb N} ratios from 11 to 19 reflecting the variation of degree of wedge contribution. Fractionation of the LREE over the HREE and fractionation of incompatible elements may be due to their heterogeneous distribution in the magma source. More highly fractionated REE patterns of Bolivian tuffs than Peruvian tuffs are attributed to variable amounts of contamination of magmas by lower crust. After the Quechua compressional event at 7 Ma, {Sr}/{Y} ratios of tuffs of the same age, erupted at 150-250 km or 250-400 km from the Peru-Chile trench, increase from southern Peru to northern Bolivia. These differences may be attributed to the subduction of a swarm oceanic lithosphere under the Bolivian Alti-plano, leading to partial melting of the sudbucted lithosphere. New FT dating of obsidian fragments of the sillar of Arequipa at 2.42 ± 0.11 Ma. This tuff dates the last Quechua compressional upper Pliocene phase ( 2.5 Ma) and confirms that the sillar is not contemporaneous with the Toba 76 tuff or the Perez ignimbrite of northern Bolivia. Geochemical characteristics of tuffs erupted before and after this last compressional phase remained the same and provide evidence that the upper Miocene ( 7 Ma) compressional deformations played the most important role on the variability of the geochemical characteristics of the southern Peruvian and northern Bolivian tuffs.

Pressurized Slot Testing to Determine Thermo-Mechanical Properties of Lithophysal Tuff at Yucca Mountain Nevada.

DOE Office of Scientific and Technical Information (OSTI.GOV)

George, James T.; Sobolik, Steven R.; Lee, Moo Y.

The study described in this report involves heated and unheated pressurized slot testing to determine thermo-mechanical properties of the Tptpll (Tertiary, Paintbrush, Topopah Spring Tuff Formation, crystal poor, lower lithophysal) and Tptpul (upper lithophysal) lithostratigraphic units at Yucca Mountain, Nevada. A large volume fraction of the proposed repository at Yucca Mountain may reside in the Tptpll lithostratigraphic unit. This unit is characterized by voids, or lithophysae, which range in size from centimeters to meters, making a field program an effective method of measuring bulk thermal-mechanical rock properties (thermal expansion, rock mass modulus, compressive strength, time-dependent deformation) over a range ofmore » temperature and rock conditions. The field tests outlined in this report provide data for the determination of thermo-mechanical properties of this unit. Rock-mass response data collected during this field test will reduce the uncertainty in key thermal-mechanical modeling parameters (rock-mass modulus, strength and thermal expansion) for the Tptpll lithostratigraphic unit, and provide a basis for understanding thermal-mechanical behavior of this unit. The measurements will be used to evaluate numerical models of the thermal-mechanical response of the repository. These numerical models are then used to predict pre- and post-closure repository response. ACKNOWLEDGEMENTS The authors would like to thank David Bronowski, Ronnie Taylor, Ray E. Finley, Cliff Howard, Michael Schuhen (all SNL) and Fred Homuth (LANL) for their work in the planning and implementation of the tests described in this report. This is a reprint of SAND2004-2703, which was originally printed in July 2004. At that time, it was printed for a restricted audience. It has now been approved for unlimited release.« less

The influence of the long-range order on the vibrational spectra of structures based on sodalite cage.

PubMed

Mikuła, A; Król, M; Koleżyński, A

2015-06-05

Zeolites are a group of tecto-aluminosilicates with numerous practical applications, e.g. gas separators, molecular sieves and sorbents. The unique properties result from porous structure of channels and cages which are built from smaller units - the so-called Secondary Building Units (SBU), and sometimes also larger groups (Breck, 1974; Ciciszwili et al., 1974; Mozgawa, 2008; Čejka and van Bekkum, 2005). The aim of this study was the examination of the influence of long-range order on vibrational spectra of sodalite and zeolite A. Ab initio calculations (geometry optimizations and vibrational spectra calculations) of sodalite cage and selected SBU were carried out by means of Gaussian09 (Frisch et al., 2009) (in the case of isolated clusters) and Crystal09 (Dovesi et al., 2005, 2009) (for periodic structures). The obtained results were compared with the experimental spectra of sodalite and zeolite A crystal structures, synthesized under hydrothermal conditions. These results allowed analyzing of the long-range ordering influence on the vibrational spectra, as well as the identification of the characteristic vibrations in β cage based frameworks. It has been found, that based on small structural fragment (SBU) models a characteristic vibrations can be identify. However, full spectra analysis and especially the interpretation of far-infrared region of the spectra require using periodic models under the influence of translational crystal lattice. Copyright © 2015 Elsevier B.V. All rights reserved.

In Situ Measurement of Permeability in the Vicinity of Faulted Nonwelded Bishop Tuff, Bishop, CA

NASA Astrophysics Data System (ADS)

Dinwiddie, C. L.; Fedors, R. W.; Ferrill, D. A.; Bradbury, K. K.

2002-12-01

The nonwelded Bishop Tuff includes matrix-supported massive ignimbrites and clast-supported bedded deposits. Fluid flow through such faulted nonwelded tuff is likely to be influenced by a combination of host rock properties and the presence of deformation features, such as open fractures, mineralized fractures, and fault zones that exhibit comminuted fault rock and clays. Lithologic contacts between fine- and coarse-grained sub-units of nonwelded tuff may induce formation of capillary and/or permeability barriers within the unsaturated zone, potentially leading to down-dip lateral diversion of otherwise vertically flowing fluid. However, discontinuities (e.g., fractures and faults) may lead to preferential sub-vertical fast flow paths in the event of episodic infiltration rates, thus disrupting the potential for both (1) large-scale capillary and/or permeability barriers to form and for (2) redirection of water flow over great lateral distances. This study focuses on an innovative technique for measuring changes in matrix permeability near faults in situ--changes that may lead to enhancement of vertical fluid flow and disruption of lateral fluid flow. A small-drillhole minipermeameter probe provides a means to eliminate extraction of fragile nonwelded tuffs as a necessity for permeability measurement. Advantages of this approach include (1) a reduction of weathering-effects on measured permeability, and (2) provision of a superior sealing mechanism around the gas injection zone. In order to evaluate the effect of faults and fault zone deformation on nonwelded tuff matrix permeability, as well as to address the potential for disruption of lithologic barrier-induced lateral diversion of flow, data were collected from two fault systems and from unfaulted host rock. Two hundred and sixty-seven gas-permeability measurements were made at 89 locations; i.e. permeability measurements were made in triplicate at each location with three flow rates. Data were collected at the first fault and perpendicularly away from it within the hanging wall to a distance of 6 m [20 ft] along one transect, and perpendicular to the fault from the foot wall to the hanging wall for a distance of 6 m [20 ft] along a second transect. Additionally, eight water-permeameter tests were conducted in order to augment the gas-permeability data. Gas-permeability measurements were collected along two transects at the main fault of the second fault system and perpendicularly away from it within the foot wall to a distance of 10.5 m [34 ft], crossing several secondary faults in the process. Data were also collected within the fault gouge of the main fault, and were found to vary therein by an order of magnitude. This Bishop Tuff study supports the U.S. Nuclear Regulatory Commission (NRC) review of hydrologic property studies at Yucca Mountain, Nevada, which are conducted by the U.S. Department of Energy. This abstract is an independent product of the CNWRA and does not necessarily reflect the views or regulatory position of the NRC.

Paleomagnetism and tectonic rotation of the lower Miocene Peach Springs Tuff: Colorado Plateau, Arizona, to Barstow, California

USGS Publications Warehouse

Wells, Ray E.; Hillhouse, John W.

1989-01-01

We have determined remanent magnetization directions of the lower Miocene Peach Springs Tuff at 41 localities in western Arizona and southeastern California. An unusual northeast and shallow magnetization direction confirms the proposed geologic correlation of isolated outcrops of the tuff from the Colorado Plateau to Barstow, California, a distance of 350 km. The Peach Springs Tuff was apparently emplaced as a single cooling unit about 18 or 19 Ma and is now exposed in 4 tectonic provinces west of the Plateau, including the Transition Zone, Basin and Range, Colorado River extensional corridor, and central Mojave Desert strike-slip zone. As such, the tuff is an ideal stratigraphic and structural marker for paleomagnetic assessment of regional variations in tectonic rotations about vertical axes. From 4 sites on the stable Colorado Plateau, we have determined a reference direction of remanent magnetization (I = 36.4°, D = 33.0°, α95 = 3.4°) that we interpret as a representation of the ambient magnetic field at the time of eruption. A steeper direction of magnetization (I = 54.8°, D = 22.5°, α95 = 2.3°) was observed at Kingman where the tuff is more than 100 m thick, and similar directions were determined at 7 other thick exposures of the Peach Springs Tuff. The steeper component is presumably a later-stage magnetization acquired after prolonged cooling of the ignimbrite. When compared to the Plateau reference direction, tilt-corrected directions from 3 of 6 sites in the central Mojave strike-slip zone show localized rotations up to 13° in the vicinity of strike-slip faults. The other three sites show no significant rotations with respect to the Colorado Plateau. Both clockwise and counterclockwise rotations were measured, and no systematic regional pattern is evident. Our results do not support kinematic models which require consistent rotation of large regions to accommodate the cumulative displacement of major post-middle Miocene strike-slip faults in the central Mojave Desert. Most of our sites in the Transition Zone and Basin and Range province have had no significant rotation, although small counterclockwise rotation in the McCullough and New York Mountains may be related to sinistral shear along en echelon faults southwest of the Lake Mead shear zone. The larger rotations occur in the Colorado River extensional corridor, where 8 of 14 sites show rotations ranging from 37° clockwise to 51° counterclockwise. These rotations occur in allochthonous tilt blocks which have been transported northeastward above the Chemehuevi-Whipple Mountains detachment fault. Upper-plate blocks within 1 km of the exposed detachment unexpectedly show no significant rotation. From this relation, we infer that rotations are accommodated along numerous low-angle faults at higher structural levels above the detachment surface.

Chemical correlation of some late Cenozoic tuffs of Northern and Central California by neutron activation analysis of glass and comparison with X-ray fluorescence analysis

USGS Publications Warehouse

Sarna-Wojcicki, Andrei M.; Bowman, Harry W.; Russell, Paul C.

1979-01-01

Glasses separated from several dacitic and rhyolitic late Cenozoic tuffs of northern and central California were analyzed by neutron activation for more than 43 elemental abundances. Eighteen elements--scandiurn, manganese, iron, zinc, rubidium, cesium, barium, lanthanum, cerium, samarium, europium, terbiurn, dysprosiurn, ytterbiurn, hafniurn, tantalurn, thorium and uranium--were selected as most suitable for purposes of chemical correlation on the basis of their natural variability in silicic tuffs and the precision obtainable in analysis. Stratigraphic relations between tuffs and replicate chemical analyses on individual tuffs make it possib1e to calibrate a quantitative parameter, the similarity coefficient, which indicates the degree of correlation for the tuffs studied. The highest similarity coefficient (0.99) was obtained for analyses of two tuffs (potassium-argon dated at about' 6.0 m.y.) exposed in the Merced(?) and Petaluma Formations of Sonoma County, which represent different paleoenvironments, shallow-water marine and fresh water or brackish marine, respectively. Corre1ation of these formations on the basis of criteria other than tephrochronoloqy would be difficult. Results of neutron activation analysis in general confirm earlier correlations made on the basis of analysis by X-ray fluorescence but also make it possible to resolve small compositional differences between chemically simi1ar tuffs in stratigraphic proximity. The Lawlor Tuff (potassium-argon dated at about 4.0 m.y.) is identified at two new localities: in a core sample obtained from a bore hole east of Suisun Bay, and from the Kettleman Hills of western San Joaquin Valley. This identification permits correlation of the uppermost part of the marine Etchegoin Formation in the San Joaquin Valley with the continental Livermore Gravels of Clark, the Tassajara Formation, and the upper part of the Sonoma Volcanics in the cel1tral Coast Ranges of California. A younger tuff near the top of the marine San Joaquin Formation in the Kettleman Hills has been identified at both new 1oca1ities .

Eruptive style and construction of shallow marine mafic tuff cones in the Narakay Volcanic Complex (Proterozoic, Hornby Bay Group, Northwest Territories, Canada)

NASA Astrophysics Data System (ADS)

Ross, Gerald M.

1986-03-01

The Early Proterozoic (1663 Ma) Narakay Volcanic Complex, exposed in Great Bear Lake (Northwest Territories, Canada), is a bimodal suite of basalt and rhyolite erupted in a continental setting and consisting largely of pyroclastic rocks interlayered with shallow marine sedimentary rocks of the Hornby Bay Group. Mafic pyroclastic rocks consist of lapilli tuff, tuff, tuff breccia and agglomerate that represent the remnants of small subaerial tuff cones (0.5 to 2 km in diameter) that in most cases have subsided into the volcanic conduit. Stratification styles, sedimentary structures and grain morphologies in pyroclastic rocks reflect variations in the water:magma ratio during eruptions and have been used to help elucidate eruptive mechanisms and reconstruct volcanic edifices. Basaltic pyroclasts are commonly bounded by fracture surfaces and are morphologically similar to modern pyroclasts produced by thermal quench fragmentation or steam-blast disruption of magma. Most fragments have low vesicularity and scoria is only locally abundant which indicates that eruptive energy was supplied mostly by water—melt interaction rather than exsolution of magmatic gases. Cored bombs and lapilli, fusiform bombs, and pyroclasts similar in texture to those of Strombolian cinder and agglutinate spatter, are uncommon but are stratigraphically widespread and imply the occurrence of Strombolian eruptions, presumably when water access to the vent was impeded. Massive bedding is typical of the tuffs and, in addition to the poorly sorted ash-rich nature of the tuffs, implies deposition from water- and/or steam-rich hydrovolcanic eruption clouds and cypressoid jets by airfall and dense pyroclastic flows. Uncommon well-stratified and sorted ash and lapilli tuff record airfall and pyroclastic flow(?) deposition from eruption clouds rich in magmatic gases. Base surge deposits are uncommon and occur only in the subaerial portion of a sequence of tuffs inferred to record the progradation of a cone-margin surge platform into standing water. Few of the tuff cone deposits display a systematic vertical sequence of stratification styles, structures and grain morphologies. This indicates that either the eruptive style varied irregularly between hydrovolcanic and Strombolian and/or that pyroclasts of different origin were mixed during eruptions.

Reconnaissance geochronology of tuffs in the Miocene Barstow Formation: implications for basin evolution and tectonics in the central Mojave Desert

USGS Publications Warehouse

Miller, David M.; Leslie, Shannon R.; Hillhouse, John W.; Wooden, Joseph L.; Vazquez, Jorge A.; Reynolds, R.E.

2010-01-01

Early to middle Miocene lacustrine strata of the Barstow Formation are well dated in just a few places, limiting our ability to infer basin evolution and regional tectonics. At the type section in the Mud Hills, previous studies have shown that the lacustrine interval of the Barstow Formation is between ~16.3 Ma and ~13.4 Ma. Elsewhere, lake beds of the Barstow Formation have yielded vertebrate fossils showing the Hemingfordian/Barstovian transition at ~16 Ma but are otherwise poorly dated. In an attempt to clarify the age and depositional environments of the lake deposits, we are mapping the Barstow Formation and dating zircons from interbedded tuffs, as well as testing ash-flow tuffs for the distinctive remanent magnetization direction of the widespread Peach Spring Tuff. Thus far, our new U-Pb zircon ages indicate that the Barstow lake beds contain tuff beds as old as 19.1 Ma and as young as 15.3 Ma. At Harvard Hill, Barstow lake beds contain a thick tuff dated at 18.7 Ma. On the basis of zircon ages, mineralogy, zircon chemistry, and paleomagnetic results, we consider the thick tuff to be a lacustrine facies of the Peach Spring Tuff. We have identified the Peach Spring Tuff by similar methods at eight localities over a broad area, providing a timeline for several fluvial and lacustrine sections. The new dates indicate that long-lived lacustrine systems originated before 19 Ma and persisted to at least 15 Ma. The onset of lacustrine conditions predates the Peach Spring Tuff in most Barstow Formation sections and may be older than 19.5 Ma in some places. The new data indicate that the central Mojave Desert contained narrow to broad lake basins during and after extension, and that Barstow lacustrine deposits did not exclusively postdate extensional tectonics. At present, it is unclear whether several separate, small lake basins coexisted during the early to middle Miocene, or if instead several small early Miocene basins gradually coalesced over about 6 million years to form one or two large middle Miocene lake basins.

Reconnaissance geochronology of tuffs in the Miocene Barstow Formation: implications for basin evolution and tectonics in the central Mojave Desert

USGS Publications Warehouse

Miller, D.M.; Leslie, S.R.; Hillhouse, J.W.; Wooden, J.L.; Vazquez, J.A.; Reynolds, R.E.

2010-01-01

Early to middle Miocene lacustrine strata of the Barstow Formation are well dated in just a few places, limiting our ability to infer basin evolution and regional tectonics. At the type section in the Mud Hills, previous studies have shown that the lacustrine interval of the Barstow Formation is between ~16.3 Ma and ~13.4 Ma. Elsewhere, lake beds of the Barstow Formation have yielded vertebrate fossils showing the Hemingfordian/Bartovian transition at ~16 Ma but are otherwise poorly dated. In an attempt to clarify the age and depositional environments of the lake deposits, we are mapping the Barstow Formation and dating zircons from interbedded tuffs, as well as testing ash-flow tuffs for the distinctive remanent magnetization direction of the widespread Peach Spring Tuff. Thus far, our new U-Pb zircon ages inficate that the Barstow lake beds contain tuff beds as old as 19.1 Ma and as young as 15.3 Ma. At Harvard Hill, Barstow lake beds contain a thick tuff dated at 18.7 Ma. On the basis of zircon ages, mineralogy, zircon chemistry, and paleomagnetic results, we consider the thick tuff to be a lacustrine facies of the Peach Spring Tuff. We have identified the Peach Spring Tuff by similar methods at eight localities over a broad area, providing a timeline for several fluvial and lacustrine sections. The new dates indicate that long-lived lacustrine systems originated before 19 Ma and persisted to at least 15 Ma. The onset of lacustrine conditions predates the Peach Spring Tuff in most Barstow Formation sections and may be older than 19.5 Ma in some places. The new data indicate that the central Mojave Desert contained narrow to broad lake basins during and after extension, and that Barstow lacustrine deposits did not exclusively postdate extensional tectonics. At present, it is unclear whether several separate, small lake basins coexisted during the early to middle Miocene, or if instead several small early Miocene basins gradually coalesced over about 6 millions years to form one or two large middle Miocene lake basins.

Antifungal activities against toxigenic Fusarium specie and deoxynivalenol adsorption capacity of ion-exchanged zeolites.

PubMed

Savi, Geovana D; Cardoso, William A; Furtado, Bianca G; Bortolotto, Tiago; Zanoni, Elton T; Scussel, Rahisa; Rezende, Lucas F; Machado-de-Ávila, Ricardo A; Montedo, Oscar R K; Angioletto, Elidio

2018-03-04

Zeolites are often used as adsorbents materials and their loaded cations can be exchanged with metal ions in order to add antimicrobial properties. The aim of this study was to use the 4A zeolite and its derived ion-exchanged forms with Zn 2+ , Li + , Cu 2+ and Co 2+ in order to evaluate their antifungal properties against Fusarium graminearum, including their capacity in terms of metal ions release, conidia germination and the deoxynivalenol (DON) adsorption. The zeolites ion-exchanged with Li + , Cu 2+ , and Co 2+ showed an excellent antifungal activity against F. graminearum, using an agar diffusion method, with a zone of inhibition observed around the samples of 45.3 ± 0.6 mm, 25.7 ± 1.5 mm, and 24.7 ± 0.6 mm, respectively. Similar results using agar dilution method were found showing significant growth inhibition of F. graminearum for ion-exchanged zeolites with Zn 2+ , Li + , Cu 2+ , and Co 2+ . The fungi growth inhibition decreased as zeolite-Cu 2+ >zeolite-Li + >zeolite-Co 2+ >zeolite-Zn 2+ . In addition, the conidia germination was strongly affected by ion-exchanged zeolites. With regard to adsorption capacity, results indicate that only zeolite-Li + were capable of DON adsorption significantly (P < 0.001) with 37% at 2 mg mL -1 concentration. The antifungal effects of the ion-exchanged zeolites can be ascribed to the interactions of the metal ions released from the zeolite structure, especially for zeolite-Li + , which showed to be a promising agent against F. graminearum and its toxin.

Design and fabrication of zeolite macro- and micromembranes

NASA Astrophysics Data System (ADS)

Chau, Lik Hang Joseph

2001-07-01

The chemical nature of the support surface influences zeolite nucleation, crystal growth and elm adhesion. It had been demonstrated that chemical modification of support surface can significantly alter the zeolite film and has a good potential for large-scale applications for zeolite membrane production. The incorporation of titanium and vanadium metal ions into the structural framework of MFI zeolite imparts the material with catalytic properties. The effects of silica and metal (i.e., Ti and V) content, template concentration and temperature on the zeolite membrane growth and morphology were investigated. Single-gas permeation experiments were conducted for noble gases (He and Ar), inorganic gases (H2, N2, SF6) and hydrocarbons (methane, n-C4, i-C4) to determine the separation performance of these membranes. Using a new fabrication method based on microelectronic fabrication and zeolite thin film technologies, complex microchannel geometry and network (<5 mum), as well as zeolite arrays (<10 mum) were successfully fabricated onto highly orientated supported zeolite films. The zeolite micropatterns were stable even after repeated thermal cycling between 303 K and 873 K for prolonged periods of time. This work also demonstrates that zeolites (i.e., Sil-1, ZSM-5 and TS-1) can be employed as catalyst, membrane or structural materials in miniature chemical devices. Traditional semiconductor fabrication technology was employed in micromachining the device architecture. Four strategies for the manufacture of zeolite catalytic microreactors were discussed: zeolite powder coating, uniform zeolite film growth, localized zeolite growth, and etching of zeolite-silicon composite film growth inhibitors. Silicalite-1 was also prepared as free-standing membrane for zeolite membrane microseparators.

Patchy distribution of magma that fed the Bishop Tuff supereruption: Evidence from matrix glass major and trace-element compositions

NASA Astrophysics Data System (ADS)

Gualda, G. A. R.; Ghiorso, M. S.; Hurst, A. A.; Allen, M. C.; Bradshaw, R. W.

2017-12-01

For more than 40 years, the Bishop Tuff has been the archetypical example of a singular, zoned magma body that fed a supereruption. Early-erupted material is pyroxene-free and crystal poor (<20 wt. %), presumably erupted from the upper parts of the magma body; late-erupted material is orthopyroxene and clinopyroxene-bearing, commonly more crystal rich (up to 30 wt. % crystals), and presumably tapped magma from the lower portions of the magma body. Fe-Ti oxide compositions suggest higher crystallization temperatures for late-erupted magmas (as high as 820 °C) than for early-erupted magmas (as low as 700 °C). Pressures and temperatures derived from major element compositions of glass inclusions led Gualda & Ghiorso (2013, CMP) to suggest an alternative model of lateral juxtaposition of two main magma bodies - each one feeding early-erupted and late-erupted units. Chamberlain et al. (2015, JPet) and Evans et al. (2016, AmMin) recently disputed this interpretation. We present a large dataset of matrix glass compositions for 161 pumice clasts that span the stratigraphy of the deposit. We calculate crystallization pressures based on major-element glass compositions using rhyolite-MELTS geobarometry, and crystallization temperatures based on Zr in glass using zircon saturation geothermometry. We apply the same methods to 1538 major-element and 615 trace-element analyses from Chamberlain et al. The results overwhelmingly demonstrate that there is no difference in crystallization temperature or pressure between early and late-erupted magmas. Crystallization pressures and temperatures are unimodal, with modes of 150 MPa and 730 °C (calibration of Watson & Harrison). Our results strongly support lateral juxtaposition of two main magma bodies. Smaller units recognized by Chamberlain et al. crystallized at the same pressures as the main bodies - this suggests the coexistence of larger and smaller magma bodies at the time of the Bishop Tuff supereruption. We compare our findings for the Bishop Tuff with results for very large and supereruptions elsewhere in the world. We argue that supereruptions typically mobilize a complex patchwork of magma bodies that reside within specific levels of the crust. They reveal moments of high-melt productivity in the crust, unlike what we observe in the Earth today.

Rhyolitic tephra record of the Gona region, southern Afar Rift, Ethiopia: Characteristics correlation and chronology

NASA Astrophysics Data System (ADS)

Dunbar, N. W.; Brown, F. H.; Levin, N. E.; McIntosh, W. C.; Rogers, M.; Semaw, S.; Simpson, S. W.; Stinchcomb, G. E.

2016-12-01

The Gona region, on the western flank of the southern Afar Rift, in Ethiopia, contains a rich and complex tephra record that provides insight into structural evolution of the region and chronological controls on the local record of human evolution. Despite lack of source volcanoes in the Gona region, thick (up to 80 cm), fine-grained (20-500 µm), fresh, pure, glassy distal tephra layers, which are discontinuous and appear to have undergone significant secondary thickening shortly after deposition, are present in sediments deposited in the last two million years. Altered tephra are present in older sediments. New data are consistent with those reported by Quade et al. (2008), showing that tephra from Gona are typically rhyolitic, consistent with derivation from large, but distant volcanic eruptions. Significant geochemical variation is observed between different tephra layers, particularly with respect to FeO (ranging between 2 and 7.5 wt.% in different rhyolitic tephra), Ca, Mn, and Cl. Elements Na and K are variable, consistent with alkali mobility during glass hydration. Although some tephra layers contain feldspar and are thus datable using the 40Ar/39Ar, others are not directly datable, so must be geochemically linked to dated source eruptions. A unit of particular focus is the widespread marker tuff known locally as the Boolihinan tuff, which is associated with significant hominin fossils and artifacts. This locally aphyric unit, which consists of highly expanded rhyolitic glass, exhibits some geochemical variability, particularly with respect to SiO2 (74-78 wt.%), but yields a robust compositions with respect to Fe, Ca, Mn, and Cl. The Boolihinan tuff was previously tentatively correlated to a 1.6 Ma tephra found in DSDP core DEM-4-1. However, we suggest here a more robust correlation to two samples of an unwelded ignimbrite with 40Ar/39Ar ages of 1.281±0.061 and 1.253±0.041 (27-01 and 27-05 of Morgan et al., 2012) from the Melka Kunture area, which is over 300 km from the Gona field area. The Boolihinan tuff is interpreted to be the ashfall equivalent of the unwelded ignimbrite. This correlation provides a chronological marker which in turn provides improved age constraints to the fossils and artifacts at Gona that are found in association with this tephra.

Radioelements and their occurrence with secondary minerals in heated and unheated tuff at the Nevada Test Site

DOE Office of Scientific and Technical Information (OSTI.GOV)

Flexser, S.; Wollenberg, H.A.

1992-06-01

Samples of devitrified welded tuff near and away from the site of a heater test in Rainier Mesa were examined with regard to whole-rock radioelement abundances, microscopic distribution of U, and oxygen isotope ratios. Wholerock U averages between 4 and 5 ppM, and U is concentrated at higher levels secondary opaque minerals as well as in accessory grains. U in primary and secondary sites is most commonly associated with Mn phases, which average {approximately}30 ppM U in more uraniferous occurrences. This average is consistent and apparently unaffected by proximity to the heater. The Mn phases differ compositionally from Mn mineralsmore » in other NTS tuffs, usually containing abundant Fe, Ti, and sometimes Ce, and are often poorly crystalline. Oxygen isotope ratios show some depletion in {delta}{sup 18}O in tuff samples very close to the heater; this depletion is consistent with isotopic exchange between the tuff and interstitial water, but it may also reflect original heterogeneity in isotopic ratios of the tuff unrelated to the heater test. Seismic properties of several tuff samples were measured. Significant differences correlating with distance from the heater occur in P- and S-wave amplitudes; these may be due to loss of bound water. Seismic velocities are nearly constant and indicate a lack of significant microcracking. The absence of clearer signs of heater-induced U mobilization or isotopic variations may be due to the short duration of the heater test, and to insufficient definition of pre-heater-test heterogeneities in the tuff.« less

Modification of Natural Zeolite with Fe(III) and Its Application as Adsorbent Chloride and Carbonate ions

NASA Astrophysics Data System (ADS)

Suhartana; Sukmasari, Emmanuella; Azmiyawati, Choiril

2018-04-01

The aim of the research is to natural zeolite with Fe(III) using anion exchange process to improve the anion exchange capacity. Natural zeolite was activated using HNO3 1 N and then mixed with FeCl3 solution and refluxed followed by oven and calcination at a temperature of 550°C. The influence of Fe(III) to zeolite was characterized by FTIR while presence of Fe in zeolite characterized by AAS. Zeolite and Zeolite-Fe adsorption capacity of chloride and carbonate anions were determined through adsorption test by variation of pH and contact time. In advanced, and then to determining the Fe adsorbed concentration at Zeolite using UV-Vis spectrophotometer. FTIR analysis result showed that the addition of Fe does not affect the zeolite’s structure but change the intensity of the zeolite spectra. The Fe concentration in Zeolite-Fe of 714 mg L-1, indicate that Fe was present in the zeolite. Both Zeolite and Zeolite-Fe adsorbtion results showed that optimum pH of Chloride anion is 2, with adsorption capacity 2,33 x 10-3 gg-1 and optimum contact time is 8 minutes. While Zeolite and Zeolite-Fe adsorbtion results showed that optimum pH of Carbonate anion is 5, with adsorption capacity 5,31 x 10-3 gg-1 and optimum contact time is 8 minutes.

Geology of Mount Rainier National Park, Washington

USGS Publications Warehouse

Fiske, Richard S.; Hopson, Clifford Andrae; Waters, Aaron Clement

1963-01-01

Mount Rainier National Park includes 378 square miles of rugged terrain on the west slope of the Cascade Mountains in central Washington. Its mast imposing topographic and geologic feature is glacier-clad Mount Rainier. This volcano, composed chiefly of flows of pyroxene andesite, was built upon alt earlier mountainous surface, carved from altered volcanic and sedimentary rocks invaded by plutonic and hypabyssal igneous rocks of great complexity. The oldest rocks in the park area are those that make up the Olmnapecosh Formation of late Eocene age. This formation is more than 10,000 feet thick, and consists almost entirely of volcanic debris. It includes some lensoid accumulations of lava and coarse mudflows, heaped around volcanic centers., but these are surrounded by vastly greater volumes of volcanic clastic rocks, in which beds of unstratified coarse tuff-breccia, about 30 feet in average thickness, alternate with thin-bedded breccias, sandstones, and siltstones composed entirely of volcanic debris. The coarser tuff-breccias were probably deposited from subaqueous volcanic mudflows generated when eruption clouds were discharged directly into water, or when subaerial ash flows and mudflows entered bodies of water. The less mobile mudflows and viscous lavas built islands surrounded by this sea of thinner bedded water-laid clastics. In compostion the lava flows and coarse lava fragments of the Ohanapecosh Formation are mostly andesite, but they include less abundant dacite, basalt, and rhyolite. The Ohanapecosh Formation was folded, regionally altered to minerals characteristic of the zeolite facies of metamorphism, uplifted, and deeply eroded before the overlying Stevens Ridge Formation of Oligocene or early Miocene age was deposited upon it. The Stevens Ridge rocks, which are about 3,000 feet in maximum total thickness, consist mainly of massive ash flows. These are now devitrified and altered, but they originally consisted of rhyodacite pumice lapilli and glass shards, which compacted and welded into thick massive units during emplacement and cooling. Subordinate water-laid clastic rocks occur t(ward the top of the formation, and thin-bedded pyroclastic layers occur between some of the ash flows. Exposures on Backbone Ridge and on Carbon River below the mouth of Cataract Creek show that in places the thick basal Stevens Ridge ash flows swept with great violence over an old erosion surface developed on rocks of the Ohanapecosh Formation. Masses of mud, tree trunks, and other surface debris were swirled upward into the base of the lowermost ash fiery, and lobes and tongues of hot ash were forced downward into. the saprolitic mud. The Stevens Ridge Formation is concordantly overlain by the Fifes Peak Formation of probable early Miocene age, which consists of lava flows, subordinate mudflows, and minor quantities of tuffaceous clastic rocks. The lavas are predominantly olivine basalt and basaltic andesite, but they include a little rhyolite. They are slightly to moderately altered: the ferromagnesian phenocrysts are generally replaced by saponite, chiprite, or carbonate ; the glass is devitrified ; and the rocks are locally permeated by veinlets of zeolite. Swarms of diabase sills and dikes are probably intrusive equivalents of the Fifes Peak lavas. The upper part of the Fifes Peak Formation has been mostly eroded from Mount Rainier National Park, but farther north, in the Cedar Lake quadrangle, it attains a thickness of more than 5,000 feet. The Fifes Peak and earlier formations were gently folded, faulted, uplifted, and eroded before the. late Miocene Tatoosh pluton worked its way upward to shallow depths and eventually broke through to the surface. The rise of the pluton was accompanied by .the injection of a complicated melange of satellitic stocks, sills, and dikes. A favored horizon for intrusion of sills was along or near the unconfo

Mineralogy and fluid content of sediments entering the Costa Rica subduction zone - Results from Site U1414, IODP Expedition 344

NASA Astrophysics Data System (ADS)

Charpentier, D.; Buatier, M.; Kutterolf, S.; Straub, S. M.; Nascimento, D.; Millan, C.

2013-12-01

Subduction zones are characterized by the largest thrust earthquakes, as quantified by both rupture area and seismic moment release. Offshore Costa Rica, the oceanic Cocos Plate subducts under the Caribbean plate forming the southern end of the Middle America trench. A high convergence rate and almost complete subduction of incoming sediments make the Costa Rica convergent margin an extremely dynamic environment. The Costa Rica Seismogenesis Project (CRISP) is designed to understand the processes that control nucleation and seismic rupture of large earthquakes at erosional subduction zones. Site U1414 of IODP Exp.344 was drilled to investigate the material from the incoming Cocos Plate. A key parameter of incoming plate is fluid content and release because it impacts deformation within the subduction complex. The deposition, compaction and diagenesis of sedimentary rocks control the distribution of fluids, fluid pressures and fluid flow patterns within subduction zones. We therefore decided to characterize sediment composition and quantify the different types of water at Site U1414. Mineralogical investigations were performed using optical and electronic microscope observations, X Ray Diffraction (on bulk and clay fractions), Cation Exchange Capacity measurements, carbon analyses (to determine carbonate contents), and sequenced extractions in NaOH (to quantify the biogenic opal content). Fluid characteristics were approached by thermal gravimetric analyses. The entire sedimentary sequence was recovered at Site U1414 and can be divided into three major sedimentary units. The first one is a hemipelagic silty clay to clay with a gradual increase of calcareous nannofossils. The dominant mineral is smectite associated in the clay fractions with kaolinite and zeolites. Small amounts of biogenic opal have been analyzed. Other minerals like quartz, feldspar and calcite are also present. The second unit is composed of nannofossil-rich calcareous ooze. The proportion of biosilica is variable and can attain 15 wt.%. Smectite and zeolites are present in smaller amount. The third unit is a lithified sandstone. Biosilica and smectite are absent, but zeolites are still present in this unit. Fluid content that can be released varies from about 15 wt.% to 40 wt.%. In shallow levels a significant proportion is pore water fluid, whereas in deeper levels water stored within minerals comprises a greater proportion of the total fluid budget. The presence of smectite yields to fluid release by dehydration and dehydroxylation at temperatures less than approximately 100°C and 500°C respectively. Transformation of biogenic opal to diagenetic silice goes to completion at temperatures of 50-100°C. It seems to be an importance source of fluid in the second unit, whereas in unit three it is zeolite water.

Effect of alkali-treatment on the characteristics of natural zeolites with different compositions.

PubMed

Ates, Ayten

2018-08-01

A series of natural zeolites with different compositions were modified by post-synthesis modification with sodium hydroxide (NaOH) solution. Natural and modified zeolites were characterized by XRD, SEM, nitrogen adsorption, FTIR, zeta potential and temperature programmed desorption of ammonia (NH 3 -TPD). The adsorption capacities of these samples were evaluated by the adsorption of manganese from aqueous solution. The treatment with NaOH led to a decrease in the surface area and microporosity of all natural zeolites as well as partly damage of the zeolite structure depending on zeolite composition. In addition, the amount of weak, medium and strong acid sites in the zeolites was changed significantly by NaOH treatment depending on zeolite composition. The NaOH treatment resulted in a four-fold improvement in adsorption capacity of natural zeolite originated from Bigadic and a twofold decrease in that of the natural zeolite originated from Manisa-Gordes. Although the improved adsorption capacity might be mainly due to modification of porosity in the zeolites and formation of hydroxysodalite, the reduced adsorption capacity of the zeolite might be mainly due to a significant deformation of the zeolite structure. The pseudo-second-order kinetic model for the adsorption of manganese on all natural and modified zeolites fits well. Copyright © 2018 Elsevier Inc. All rights reserved.

Geoengineering properties of potential repository units at Yucca Mountain, southern Nevada

DOE Office of Scientific and Technical Information (OSTI.GOV)

Tillerson, J.R.; Nimick, F.B.

1984-12-01

The Nevada Nuclear Waste Storage Investigations (NNWSI) Project is currently evaluating volcanic tuffs at the Yucca Mountain site, located on and adjacent to the Nevada Test Site, for possible use as a host rock for a radioactive waste repository. The behavior of tuff as an engineering material must be understood to design, license, construct, and operate a repository. Geoengineering evaluations and measurements are being made to develop confidence in both the analysis techniques for thermal, mechanical, and hydrothermal effects and the supporting data base of rock properties. The analysis techniques and the data base are currently used for repository design,more » waste package design, and performance assessment analyses. This report documents the data base of geoengineering properties used in the analyses that aided the selection of the waste emplacement horizon and in analyses synopsized in the Environmental Assessment Report prepared for the Yucca Mountain site. The strategy used for the development of the data base relies primarily on data obtained in laboratory tests that are then confirmed in field tests. Average thermal and mechanical properties (and their anticipated variations) are presented. Based upon these data, analyses completed to date, and previous excavation experience in tuff, it is anticipated that existing mining technology can be used to develop stable underground openings and that repository operations can be carried out safely.« less

Re-collection of Fish Canyon Tuff for fission-track standardization

USGS Publications Warehouse

Naeser, C.W.; Cebula, G.T.

1984-01-01

The PURPOSE of this note is to announce the availability of apatite and zircon from a third collection of the Oligocene Fish Canyon Tuff (FC-3). Apatite and zircon separated from the Fish Canyon Tuff have prove to be a useful standard for fission-track dating, both for interlaboratory comparisons and for checking procedures within a laboratory. In May 1981, about 540 kg of Fish Canyon Tuff were collected for mineral separation. Approximately 7. 5 g of apatite, 6. 5 g of zircon, and 89 g of sphene were recovered from this collection. This new material is now ready for distribution.

Rejuvenation Stage Volcanics at Laeo Kilauea, Kauai, Hawaii

NASA Astrophysics Data System (ADS)

Thordarson, T.; Garcia, M.; Wanless, D.; Tagami, T.; Sano, H.

2005-12-01

The Plio-Pleistocene Koloa volcanic series represents the rejuvenated volcanism on Kauai, one of the oldest main Hawaiian Islands. The Koloa series is made up of highly alkalic basalt and associated sedimentary rocks that rest unconformably on the shield-building Waimea Canyon volcanic series. Koloa vents are dispersed across the eastern two-thirds of the island and typically consist of scoria or lava cones that fed broad lava flow fields blanketing the marginal lowlands on the south, east and north side of the island. The northernmost subaerial Koloa vents are found at Laeo Kilauea on the north shore of the island. At Laeo Kilauea the volcanic succession is unusual in that it contains the only phreatomagmatic vent structures of the Koloa series. Here an ~2-km-long costal cliff face reveals a bedded phreatomagmatic tephra sequence that is >90-m-thick and represents the remnant of an a much large tuff cone (>2-km in diameter). The tuff cone sequence is characterized by decimeter to meters thick layers, where cross-bedded ash beds alternate with massive and poorly sorted lapilli tuff beds. The cross-bedded deposits were produced by dry and wet surges, whereas the poorly sorted beds represent fall deposits produced by sustained eruption column (i.e. continuous up-rush) or tephra jets (i.e. rooster-tail explosions). The juvenile clast population of the tephra consists of olivine-phyric foidite, but it also contains abundant wall-rock lithics, including fragments of reef-limestone. The base of the tuff cone outcrops at Mokolea point on the east side of the outcrop, where phreatomagmatic tephra rests directly on an older Koloa pahoehoe flow, a olivine- and mellelite-phyric foidite lava. The tephra sequence is cut by an ~1-m-thick olivine-bearing basanite dike, which acted as a feeder for the fountain-fed spatter and lava (up to 100-m-thick) that cap the phreatomagmatic tephra sequence. These units are separated by a 2-3 m thick soil horizon formed by weathering of the tuff. These three formations have been dated by Ar-Ar giving 2.65 +/- 0.35 Ma for the age of the basal foidite lava, 1.68 +/- 0.11 Ma for the tuff cone and 0.69 +/- 0.03 Ma for the overlying fountain-fed basanite lava. Important conclusions that can be drawn from the results of this study include: (1) The characteristics of the phreatomagmatic tephra indicate that at times the tuff cone crater was filled with water implying that the eruption site was submarine and most likely located in shallow coastal waters. The presence of reef-limestone fragments in the tephra supports this notion. On the other hand, the underlying and overlying lava flows, which do extend an unknown distance beyond the current shoreline, were clearly deposited on dry land. This implies that Kauai experienced significant changes in sea level in early to mid Pleistocene times. (2) The eruptions that produced the tuff cone and the overlying fountain-fed basanite lava are one million years apart, yet the dikes that fed these eruptions appear to have followed a similar path to the surface. This indicates that the magma is utilizing preexisting structural weaknesses to reach the surface.

Refinement of the crystal structures of biomimetic weddellites produced by microscopic fungus Aspergillus niger

NASA Astrophysics Data System (ADS)

Rusakov, A. V.; Frank-Kamenetskaya, O. V.; Gurzhiy, V. V.; Zelenskaya, M. S.; Izatulina, A. R.; Sazanova, K. V.

2014-05-01

The single-crystal structures of four biomimetic weddellites CaC2O4 · (2 + x)H2O with different contents of zeolitic water ( x = 0.10-0.24 formula units) produced by the microscopic fungus Aspergillus niger were refined from X-ray diffraction data ( R = 0.029-0.038). The effect of zeolitic water content on the structural stability of weddellite was analyzed. The parameter a was shown to increase with increasing x due to the increase in the distance between water molecules along this direction. The water content and structural parameters of the synthesized weddellites are similar to those of weddellites from biofilms and kidney stones.

Temperature dependence of the Henry's law constant for hydrogen storage in NaA zeolites: a Monte Carlo simulation study.

PubMed

Sousa, João Miguel; Ferreira, António Luís; Fagg, Duncan Paul; Titus, Elby; Krishna, Rahul; Gracio, José

2012-08-01

Grand canonical Monte Carlo simulations of hydrogen adsorption in zeolites NaA were carried out for a wide range of temperatures between 77 and 300 K and pressures up to 180 MPa. A potential model was used that comprised of three main interactions: van der Waals, coulombic and induced polarization by the electric field in the system. The computed average number of adsorbed molecules per unit cell was compared with available results and found to be in agreement in the regime of moderate to high pressures. The particle insertion method was used to calculate the Henry coefficient for this model and its dependence on temperature.

Biodiesel synthesis via transesterification of lipid Chlorophyta cultivated in walne rich carbon medium using KOH/Zeolite catalyst

NASA Astrophysics Data System (ADS)

Dianursanti, Hayati, Siti Zahrotul; Putri, Dwini Normayulisa

2017-11-01

Microalgae from the Chlorophyta division such as Nannochloropsis oculata and Chlorella vulgaris are highly potential to be developed as biodiesel feedstocks because they have a high oil content up to 58%. Biodiesel is produced by transesterification of triglycerides and alcohols with the aid of homogeneous catalysts such as KOH. However, the use of KOH catalysts produces soaps in the biodiesel synthesis. Heterogeneous catalysts are known to solve this problem. One of them is natural zeolite. Zeolite can be used as a catalyst and as a support catalyst. Loading KOH on the zeolite surface is expected to increase alkalinity in KOH/Zeolite catalysts so as to increase the activity of KOH/Zeolite catalyst in transesterification of triglyceride with methanol. In this experimental lipid of microalgae will be used for produced biodiesel via transesterification reaction with methanol and KOH/Zeolite as a catalyst heterogeneous at 60 °C for 3h and utilized catalyst modificated KOH/Zeolite with variation 0.5 M, 1 M and 1.5 M KOH. The modified zeolite was then analyzed by XRF, XRD and BET. The result showed that the yield of biodiesel from lipid N.oculata was 81,09% by 0.5KOH/Zeolite catalyst, 86,53% by 1KOH/Zeolite catalyst, 1,5KOH/Zeolite and 88,13% by 1.5KOH/Zeolit, while the biodiesel produced from lipid C.vulgaris was 59.29% by 0.5KOH/Zeolite, 82.27% by 1KOH/Zeolite and 83.72% by 1.5KOH/Zeolite.

Fabrication of 6FDA-durene membrane incorporated with zeolite T and aminosilane grafted zeolite T for CO2/CH4 separation

NASA Astrophysics Data System (ADS)

Jusoh, Norwahyu; Fong Yeong, Yin; Keong Lau, Kok; Shariff, Azmi Mohd

2017-08-01

In the present work, zeolite T and aminosilane grafted zeolite T are embedded into 6FDA-durene polyimide phase for the fabrication of mixed matrix membranes (MMMs). FESEM images demonstrated that the improvement of interfacial adhesion between zeolite and polymer phases in MMM loaded with aminosilane grafted zeolite T was not significant as compared to zeolite T/6FDA-durene MMM. From the gas permeation test, CO2/CH4 selectivity up to 26.4 was achieved using MMM containing aminosilane grafted zeolite T, while MMM loaded with ungrafted zeolite T showed CO2/CH4 selectivity of 19.1. In addition, MMM incorporated with aminosilane grafted zeolite T particles successfully lies on Robeson upper bound 2008, which makes it an attractive candidate for CO2/CH4 separation.

The Widespread Distribution of Komatiitic Tuffs in the 3.3 Ga Weltevreden Formation, Barberton Greenstone Belt, South Africa

NASA Astrophysics Data System (ADS)

Thompson, M. E.; Lowe, D. R.; Byerly, G. R.

2007-12-01

The 3.5-3.2 Ga Barberton greenstone belt is a heavily deformed, 10-15 km thick succession of volcanic and sedimentary rocks representing one of the best preserved Paleoarchean supracrustal sequences known. It consists of the basal volcanic-dominated Onverwacht Group and the overlying sedimentary-dominated Fig Tree and Moodies Groups. Major volcanic rocks in the BGB include komatiites, tholeiitic basalts, and dacites. Although flow rocks and fragmental deposits have been identified representing all extrusive magma types, the abundance of komatiitic volcaniclastic units is remarkable considering the mechanical difficulties in explosively erupting low viscosity ultramafic lava. In the Onverwacht Group, most komatiitic tuffs contain 85-95 wt% SiO2, due to early silicification, and very low concentrations of most other elements, making original compositions somewhat uncertain. However, in the northernmost part of the BGB, north of the Inyoka Fault, the ~ 3.3 Ga Weltevreden Formation is composed largely of komatiitic flow rocks, tuffs, layered ultramafic complexes, and subordinate black and banded cherts. Previous studies have established the extrusive nature of the komatiites, but there are also many thick interlayered slaty units, previously interpreted as sheared flow rocks, which show cross-bedding, soft-sediment deformation, and other features indicating an alternate derivation. These units range from 2 to 80 m thick and may represent 10% or more of the overall stratigraphy of the Weltevreden Formation. They are characterized by low-temperature serpentinization that has commonly preserved original elemental abundances, enabling a more precise determination of primary komatiitic liquid composition. These rocks are magnesium rich, with MgO ranging from 23 to 36 wt%, and high Ni (~1500 ppm) and Cr (~2600 ppm) contents typical of komatiites. Several possible mechanisms could have produced these rocks, including (1) erosion and transport of pre-existing komatiitic flow rock, (2) volcanic base surges, (3) current reworking of fall-deposited pyroclastic material, and (4) remobilization of hyaloclastitic debris. The abundance of fine-grained sediments and of flat- and cross-laminated beds, the paucity of cr-spinels, and komatiitic immobile element ratios suggest that most of these high-Mg beds formed by minor reworking of komatiitic pyroclastic ash in a subaqueous environment.

Catalase-like activity studies of the manganese(II) adsorbed zeolites

NASA Astrophysics Data System (ADS)

ćiçek, Ekrem; Dede, Bülent

2013-12-01

Preparation of manganese(II) adsorbed on zeolite 3A, 4A, 5A. AW-300, ammonium Y zeolite, organophilic, molecular sieve and catalase-like enzyme activity of manganese(II) adsorbed zeolites are reported herein. Firstly zeolites are activated at 873 K for two hours before contact manganese(II) ions. In order to observe amount of adsorption, filtration process applied for the solution. The pure zeolites and manganese(II) adsorbed zeolites were analysed by FT-IR. As a result according to the FT-IR spectra, the incorporation of manganese(II) cation into the zeolite structure causes changes in the spectra. These changes are expected particularly in the pseudolattice bands connected with the presence of alumino and silicooxygen tetrahedral rings in the zeolite structure. Furthermore, the catalytic activities of the Mn(II) adsorbed zeolites for the disproportionation of hydrogen peroxide were investigated in the presence of imidazole. The Mn(II) adsorbed zeolites display efficiency in the disproportion reactions of hydrogen peroxide, producing water and dioxygen in catalase-like activity.

Removal of Ca2+ and Zn2+ from aqueous solutions by zeolites NaP and KP.

PubMed

Yusof, Alias Mohd; Malek, Nik Ahmad Nizam Nik; Kamaruzaman, Nurul Asyikin; Adil, Muhammad

2010-01-01

Zeolites P in sodium (NaP) and potassium (KP) forms were used as adsorbents for the removal of calcium (Ca2+) and zinc (Zn2+) cations from aqueous solutions. Zeolite KP was prepared by ion exchange of K+ with Na+ which neutralizes the negative charge of the zeolite P framework structure. The ion exchange capacity of K+ on zeolite NaP was determined through the Freundlich isotherm equilibrium study. Characterization of zeolite KP was determined using infrared spectroscopy and X-ray diffraction (XRD) techniques. From the characterization, the structure of zeolite KP was found to remain stable after the ion exchange process. Zeolites KP and NaP were used for the removal of Ca and Zn from solution. The amount of Ca2+ and Zn2+ in aqueous solution before and after the adsorption by zeolites was analysed using the flame atomic absorption spectroscopy method. The removal of Ca2+ and Zn2+ followed the Freundlich isotherm rather than the Langmuir isotherm model. This result also revealed that zeolite KP adsorbs Ca2+ and Zn2+ more than zeolite NaP and proved that modification of zeolite NaP with potassium leads to an increase in the adsorption efficiency of the zeolite. Therefore, the zeolites NaP and KP can be used for water softening (Ca removal) and reducing water pollution/toxicity (Zn removal).

Geological monitoring of Surtsey, Iceland, 1967-1998

USGS Publications Warehouse

Jakobsson, Sveinn P.; Gudmundsson, Gudmundur; Moore, James G.

2000-01-01

Aspects of the geological monitoring of the volcanic island of Surtsey 1967-1998, are described. A hydrothermal system was developed within the tephra craters in late 1966 to early 1967. Temperatures in a drill hole, situated at the eastern border of the hydrothermal area, indicate that the hydrothermal system at that site has been cooling at an average rate of ≤ 1°C per year since 1980. The tephra was altered rapidly within the hydrothermal area, producing the first visible palagonite tuff in 1969. A substantial part of the tephra pile above sea level was probably converted to tuff by 1972. The visible area of tuff has gradually increased since then, primarily due to erosion of tephra at the surface. By 1998 52% of the exposed tephra area had been converted to palagonite tuff. By volume, however, some 80-85% of the tephra pile above sea level has been converted to tuff in 1998. The area of Surtsey has shrunk from its original 2.65 km2 (1967) to 1.47 km2 (1998) due to marine abrasion. The geological formations on Surtsey have, however, responded quite variably to erosion. The tephra pile was easily eroded, but marine abrasion. The central core of palagonite tuff is estimated to be ≤0.39 km2. Statistical estimation of models of the decreases of Surtsey indicate that it will last for a long time. The numerical experiments indicate that it will take over 100 years until only the palagonite tuff core is left. It is postulated that the final remnany of Surtsey before complete destruction will be a palagonite tuff crag, comparable to those of the other islands in the Vestmannaeyjar archipelago.

Recrystallization and anatexis along the plutonic-volcanic contact of the Turkey Creek caldera, Arizona

USGS Publications Warehouse

du Bray, E.A.; Pallister, J.S.

1999-01-01

Unusual geologic and geochemical relations are preserved along the contact between intracaldera tuff and a resurgent intrusion within the 26.9 Ma Turkey Creek caldera of southeast Arizona. Thick intracaldera tuff is weakly argillically altered throughout, except in zones within several hundred meters of its contact with the resurgent intrusion, where the groundmass of the tuff has been variably converted to granophyre and unaltered sanidine phenocrysts are present. Dikes of similarly granophyric material originate at the tuff-resurgent intrusion contact and intrude overlying intracaldera megabreccia and tuff. Field relations indicate that the resurgent intrusion is a laccolith and that it caused local partial melting of adjacent intracaldera tuff. Geochemical and petrographic relations indicate that small volumes of partially melted intracaldera tuff assimilated and mixed with dacite of the resurgent intrusion along their contact, resulting in rocks that have petrographic and compositional characteristics transitional between those of tuff and dacite. Some of this variably contaminated, second-generation magma coalesced, was mobilized, and was intruded into overlying intracaldera rocks. Interpretation of the resurgent intrusion in the Turkey Creek and other calderas as intracaldera laccoliths suggests that intrusions of this type may be a common, but often unrecognized, feature of calderas. Development of granophyric and anatectic features such as those described here may be equally common in other calderas. The observations and previously undocumented processes described here can be applied to identification and interpretation of similarly enigmatic relations and rocks in other caldera systems. Integration of large-scale field mapping with detailed petrographic and chemical data has resulted in an understanding of otherwise intractable but petrologically important caldera-related features.

Structure, stratigraphy, and eruption chronology of the Hanauma Bay Tuff Ring, Oahu, Hawaii

NASA Astrophysics Data System (ADS)

Rottas, K. M.; Houghton, B. F.

2010-12-01

The Hanauma Bay-Koko Head Complex is one of several volcanic landforms along the Koko fissure, in southeastern Oahu, that formed during rejuvenated volcanism. The Hanauma Bay region of the complex is comprised of two nested tuff rings. The internal structure of the inner tuff ring is well exposed due to subsequent breaching and wave erosion and is described in detail here for the first time. The inner tuff ring is currently believed to have formed during a single eruption episode. However, field observations, detailed photography, structural mapping in both the vertical and horizontal planes, extensive measurements of bedding attitudes, and stratigraphic analysis suggest that there were a minimum of five distinct intervals of deposition, which also blanketed the deposits of the outer tuff ring with ejecta. These intervals of sedimentation were separated by significant collapses, generating major unconformities that cross the inner wall of the inner ring. The planes of failure are marked by smaller steep-walled channels and gullies, eroded by rainfall-induced runoff and suggesting the failures were each followed by short time breaks with erosion. Within each pyroclastic sequence there are also smaller slump scars and local unconformities. The inner tuff ring was predominately formed by pyroclastic surges, although the beds of Phase 3 are primarily fall deposits. From ballistic trajectories and bedding features, it is apparent that the eruption locus shifted a minimum of two times during tuff ring growth. Ballistic blocks in the final Phase 5 indicate that the Hanauma Bay eruption was contemporaneous with a separate eruption to the north, most likely that of the Kahauloa tuff ring 880 meters away.

Performance of single-pass and by-pass multi-step multi-soil-layering systems for low-(C/N)-ratio polluted river water treatment.

PubMed

Wei, Cai-Jie; Wu, Wei-Zhong

2018-09-01

Two kinds of hybrid two-step multi-soil-layering (MSL) systems loaded with different filter medias (zeolite-ceramsite MSL-1 and ceramsite-red clay MSL-2) were set-up for the low-(C/N)-ratio polluted river water treatment. A long-term pollutant removal performance of these two kinds of MSL systems was evaluated for 214 days. By-pass was employed in MSL systems to evaluate its effect on nitrogen removal enhancement. Zeolite-ceramsite single-pass MSL-1 system owns outstanding ammonia removal capability (24 g NH 4 + -Nm -2 d -1 ), 3 times higher than MSL-2 without zeolite under low aeration rate condition (0.8 × 10 4  L m -2 .h -1 ). Aeration rate up to 1.6 × 10 4  L m -2 .h -1 well satisfied the requirement of complete nitrification in first unit of both two MSLs. However, weak denitrification in second unit was commonly observed. By-pass of 50% influent into second unit can improve about 20% TN removal rate for both MSL-1 and MSL-2. Complete nitrification and denitrification was achieved in by-pass MSL systems after addition of carbon source with the resulting C/N ratio up to 2.5. The characters of biofilms distributed in different sections inside MSL-1 system well illustrated the nitrogen removal mechanism inside MSL systems. Two kinds of MSLs are both promising as an appealing nitrifying biofilm reactor. Recirculation can be considered further for by-pass MSL-2 system to ensure a complete ammonia removal. Copyright © 2018 Elsevier Ltd. All rights reserved.

Enhanced selectivity of zeolites by controlled carbon deposition

DOEpatents

Nenoff, Tina M.; Thoma, Steven G.; Kartin, Mutlu

2006-05-09

A method for carbonizing a zeolite comprises depositing a carbon coating on the zeolite pores by flowing an inert carrier gas stream containing isoprene through a regenerated zeolite at elevated temperature. The carbonized zeolite is useful for the separation of light hydrocarbon mixtures due to size exclusion and the differential adsorption properties of the carbonized zeolite.

The spectroscopic study of building composites containing natural sorbents.

PubMed

Król, M; Mozgawa, W

2011-08-15

This work presents the results of FT-IR spectroscopic studies of heavy metal cations (Ag(+), Pb(2+), Zn(2+), Cd(2+) and Cr(3+)) immobilization from aqueous solutions on natural sorbents. The sorption has been conducted on sodium forms of zeolite (clinoptilolite) and clay minerals (mixtures containing mainly montmorillonite and kaolinite) which have been separated from natural Polish deposit. In the next part of the work both sorbents were used to obtain new building composites. It was proven those heavy metal cations' sorption causes changes in IR spectra of the zeolite and clay minerals. These alterations are dependent on the way the cations were sorbed. In the case of zeolite, variations of the bands corresponding to the characteristic ring vibrations have been observed. These rings occur in pseudomolecular complexes 4-4-1 (built of alumino- and silicooxygen tetrahedra) which constitute the secondary building units (SBU) and form spatial framework of the zeolite. The most significant changes have been determined in the region of pseudolattice vibrations (650-700 cm(-1)). In the instance of clay minerals, changes in the spectra occur at two ranges: 1200-800 cm(-1)--the range of the bands assigned to asymmetric Si-O(Si,Al) and bending Al-OH vibrations and 3800-3000 cm(-1)--the range of the bands originating from OH(-) groups stretching vibrations. Next results indicate possibilities of applying the used natural sorbents for the obtainment of new building materials having favourable composition and valuable properties. The zeolite was used for obtaining autoclaved materials with an addition of CaO, and the clay minerals for ceramic sintered materials with an addition of quartz and clinoptilolite were produced. FT-IR studies were also conducted on the obtained materials. Copyright © 2010 Elsevier B.V. All rights reserved.

Ultra-selective high-flux membranes from directly synthesized zeolite nanosheets

DOE Office of Scientific and Technical Information (OSTI.GOV)

Jeon, Mi Young; Kim, Donghun; Kumar, Prashant

A zeolite with structure type MFI is an aluminosilicate or silicate material that has a three-dimensionally connected pore network, which enables molecular recognition in the size range 0.5-0.6 nm. These micropore dimensions are relevant for many valuable chemical intermediates, and therefore MFI-type zeolites are widely used in the chemical industry as selective catalysts or adsorbents. As with all zeolites, strategies to tailor them for specific applications include controlling their crystal size and shape. Nanometre-thick MFI crystals (nanosheets) have been introduced in pillared and self-pillared (intergrown) architectures, offering improved mass-transfer characteristics for certain adsorption and catalysis applications. Moreover, single (non-intergrown andmore » nonlayered) nanosheets have been used to prepare thin membranes that could be used to improve the energy efficiency of separation processes. However, until now, single MFI nanosheets have been prepared using a multi-step approach based on the exfoliation of layered MFI9,15, followed by centrifugation to remove non-exfoliated particles. This top-down method is time-consuming, costly and low-yield and it produces fragmented nanosheets with submicrometre lateral dimensions. Alternatively, direct (bottom-up) synthesis could produce high-aspect-ratio zeolite nanosheets, with improved yield and at lower cost. Here we use a nanocrystal-seeded growth method triggered by a single rotational intergrowth to synthesize high-aspect-ratio MFI nanosheets with a thickness of 5 nanometres (2.5 unit cells). These high-aspect-ratio nanosheets allow the fabrication of thin and defect-free coatings that effectively cover porous substrates. Finally, these coatings can be intergrown to produce high-flux and ultra-selective MFI membranes that compare favourably with other MFI membranes prepared from existing MFI materials (such as exfoliated nanosheets or nanocrystals).« less

Ultra-selective high-flux membranes from directly synthesized zeolite nanosheets

DOE PAGES

Jeon, Mi Young; Kim, Donghun; Kumar, Prashant; ...

2017-03-15

A zeolite with structure type MFI is an aluminosilicate or silicate material that has a three-dimensionally connected pore network, which enables molecular recognition in the size range 0.5-0.6 nm. These micropore dimensions are relevant for many valuable chemical intermediates, and therefore MFI-type zeolites are widely used in the chemical industry as selective catalysts or adsorbents. As with all zeolites, strategies to tailor them for specific applications include controlling their crystal size and shape. Nanometre-thick MFI crystals (nanosheets) have been introduced in pillared and self-pillared (intergrown) architectures, offering improved mass-transfer characteristics for certain adsorption and catalysis applications. Moreover, single (non-intergrown andmore » nonlayered) nanosheets have been used to prepare thin membranes that could be used to improve the energy efficiency of separation processes. However, until now, single MFI nanosheets have been prepared using a multi-step approach based on the exfoliation of layered MFI9,15, followed by centrifugation to remove non-exfoliated particles. This top-down method is time-consuming, costly and low-yield and it produces fragmented nanosheets with submicrometre lateral dimensions. Alternatively, direct (bottom-up) synthesis could produce high-aspect-ratio zeolite nanosheets, with improved yield and at lower cost. Here we use a nanocrystal-seeded growth method triggered by a single rotational intergrowth to synthesize high-aspect-ratio MFI nanosheets with a thickness of 5 nanometres (2.5 unit cells). These high-aspect-ratio nanosheets allow the fabrication of thin and defect-free coatings that effectively cover porous substrates. Finally, these coatings can be intergrown to produce high-flux and ultra-selective MFI membranes that compare favourably with other MFI membranes prepared from existing MFI materials (such as exfoliated nanosheets or nanocrystals).« less

New ion-exchanged zeolite derivatives: antifungal and antimycotoxin properties against Aspergillus flavus and aflatoxin B1

NASA Astrophysics Data System (ADS)

Savi, Geovana D.; Cardoso, Willian A.; Furtado, Bianca G.; Bortolotto, Tiago; Da Agostin, Luciana O. V.; Nones, Janaína; Torres Zanoni, Elton; Montedo, Oscar R. K.; Angioletto, Elidio

2017-08-01

Zeolites are microporous crystalline hydrated aluminosilicates with absorbent and catalytic properties. This material can be used in many applications in stored-pest management such as: pesticide and fertilizer carriers, animal feed additives, mycotoxin binders and food packaging materials. Herein, four 4A zeolite forms were prepared by ion-exchange and their antifungal effect against Aspergillus flavus was highlighted. Additionally, the antimycotoxin activity and the aflatoxin B1 (AFB1) adsorption capacity of these zeolites as well as their toxic effects on Artemia sp. were investigated. The ion-exchanged zeolites with Li+ and Cu2+ showed the best antifungal activity against A. flavus, including effects on conidia germination and hyphae morphological alterations. Regarding to antimycotoxin activity, all zeolite samples efficiently inhibited the AFB1 production by A. flavus. However, the ion-exchanged zeolites exhibited better results than the 4A zeolite. On the other hand, the AFB1 adsorption capacity was only observed by the 4A zeolite and zeolite-Li+. Lastly, our data showed that all zeolites samples used at effective concentrations for antifungal and antimycotoxin assays (2 mg ml-1) showed no toxic effects towards Artemia sp. Results suggest that some these ion-exchanged zeolites have great potential as an effective fungicide and antimycotoxin agent for agricultural and food safety applications.

Surfactant modified zeolite as amphiphilic and dual-electronic adsorbent for removal of cationic and oxyanionic metal ions and organic compounds.

PubMed

Tran, Hai Nguyen; Viet, Pham Van; Chao, Huan-Ping

2018-01-01

A hydrophilic Y zeolite was primarily treated with sodium hydroxide to enhance its cation exchange capacity (Na-zeolite). The organo-zeolite (Na-H-zeolite) was prepared by a modification process of the external surface of Na-zeolite with a cationic surfactant (hexadecyltrimethylammonium; HDTMA). Three adsorbents (i.e., pristine zeolite, Na-zeolite, and Na-H-zeolite) were characterized with nitrogen adsorption/desorption isotherms, scanning electron microscopy coupled with energy dispersive X-ray spectroscopy, cation exchange capacities, and zeta potential. Results demonstrated that HDTMA can be adsorbed on the surface of Na-zeolite to form patchy bilayers. The adsorption capacity of several hazardous pollutants (i.e., Pb 2+ , Cu 2+ , Ni 2+ , Cr 2 O 7 2- , propylbenzene, ethylbenzene, toluene, benzene, and phenol) onto Na-H-zeolite was investigated in a single system and multiple-components. Adsorption isotherm was measured to further understand the effects of the modification process on the adsorption behaviors of Na-H-zeolite. Adsorption performances indicated that Na-H-zeolite can simultaneously adsorb the metal cations (on the surface not covered by HDTMA), oxyanions (on the surface covered by HDTMA). Na-H-zeolite also exhibited both hydrophilic and hydrophobic surfaces to uptake organic compounds with various water solubilities (from 55 to 75,000mg/L). It was experimentally concluded that Na-H-zeolite is a potential dual-electronic and amphiphilic adsorbent for efficiently removing a wide range of potentially toxic pollutants from aquatic environments. Copyright © 2017 Elsevier Inc. All rights reserved.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Liu Yingya; Grzywa, Maciej; Weil, Matthias

A novel metal-organic framework (MOF) based on a tetranuclear copper cluster and a linear organic ligand formulated as [Cu{sub 4}OCl{sub 6}(DABCO){sub 2}].0.5DABCO.4CH{sub 3}OH (denoted as MFU-5, MFU=Metal-Organic Framework, Ulm University; DABCO=1,4-diazabicyclo[2.2.2]octane), was prepared via solvothermal synthesis. In contrast with common MOF synthesis strategies, MFU-5 is assembled from pre-defined molecular secondary building units, i.e. {l_brace}Cu{sub 4}OCl{sub 6}{r_brace} moieties, which become the nodes of the coordination framework. The title compound was characterized by single crystal X-ray diffraction, variable temperature powder diffraction (VT-XRPD), thermal analysis, as well as IR- and UV/Vis spectroscopy. Crystal data for MFU-5: hexagonal, P6/mcc (no. 192), a=25.645(9), c=17.105(11) A,more » V=9742(8) A{sup 3}, Z=12, 1690 structure factors, R[F{sup 2}>2sigma(F{sup 2})]=0.049. MFU-5 is a 3D metal-organic framework with 1D channels running along the c-axis hosting DABCO and methanol solvent molecules. The framework displays a zeolite-like structure constructed from mso cages, which represents the composite building units in the zeolites SSF, MSO and SZR. Two-fold interpenetration is observed between these building units. TG/DTA-MS and VT-XRPD characterization reveal a stepwise release of methanol and DABCO molecules upon heating, eventually resulting in a structural change into a non-porous material. - Graphical abstract: The metal-organic framework [Cu{sub 4}OCl{sub 6}(DABCO){sub 2}].0.5DABCO.4CH{sub 3}OH (MFU-5) is constructed from a molecular precursor containing {l_brace}Cu{sub 4}OCl{sub 6}{r_brace} secondary building units which become cross-linked into a 3D zeolite-type network with hexagonal symmetry by linear DABCO ligands (DABCO=1,4-diazabicyclo[2.2.2]octane).« less

Determining the physical and chemical processes behind four caldera-forming eruptions in rapid succession in the San Juan caldera cluster, Colorado, USA

NASA Astrophysics Data System (ADS)

Curry, A. C.; Caricchi, L.; Lipman, P. W.

2017-12-01

A primary goal of volcanology is to understand the frequency and magnitude of large, explosive volcanic eruptions to mitigate their impact on society. Recent studies show that the average magma flux and the time between magma injections into a given magmatic-volcanic system fundamentally control the frequency and magnitude of volcanic eruptions, yet these parameters are unknown for many volcanic regions on Earth. We focus on major and trace element chemistry of individual phases and whole-rock samples, initial zircon ID-TIMS analyses, and zircon SIMS oxygen isotope analyses of four caldera-forming ignimbrites from the San Juan caldera cluster in the Southern Rocky Mountain volcanic field, Colorado, to determine the physical and chemical processes leading to large eruptions. We collected outflow samples along stratigraphy of the three caldera-forming ignimbrites of the San Luis caldera complex: the Rat Creek Tuff ( 150 km3), Cebolla Creek Tuff ( 250 km3), and Nelson Mountain Tuff (>500 km3); and we collected samples of both outflow and intracaldera facies of the Snowshoe Mountain Tuff (>500 km3), which formed the Creede caldera. Single-crystal sanidine 40Ar/39Ar ages show that these large eruptions occurred in rapid succession between 26.91 ± 0.02 Ma (Rat Creek Tuff) and 26.87 ± 0.02 Ma (Snowshoe Mountain Tuff), providing an opportunity to investigate the temporal evolution of magmatic systems feeding large, explosive volcanic eruptions. Major and trace element analyses show that the first and last eruption of the San Luis caldera complex (Rat Creek Tuff and Nelson Mountain Tuff) are rhyolitic to dacitic ignimbrites, whereas the Cebolla Creek Tuff and Snowshoe Mountain Tuff are crystal-rich, dacitic ignimbrites. Trace elements show enrichment in light rare-earth elements (LREEs) over heavy rare-earth elements (HREEs), and whereas the trace element patterns are similar for each caldera cycle, trace element values for each ignimbrite show variability in HREE concentrations. This variability indicates that these large eruptions sampled a magmatic system with some degree of internal heterogeneity. These results have implications for the chemical and physical processes, such as magmatic flux and injection periodicity, leading to the formation of large magmatic systems prior to large, explosive eruptions.

Use of infrared spectroscopy for the determination of electronegativity of rare earth elements.

PubMed

Frost, Ray L; Erickson, Kristy L; Weier, Matt L; McKinnon, Adam R; Williams, Peter A; Leverett, Peter

2004-07-01

Infrared spectroscopy has been used to study a series of synthetic agardite minerals. Four OH stretching bands are observed at around 3568, 3482, 3362, and 3296 cm(-1). The first band is assigned to zeolitic, non-hydrogen-bonded water. The band at 3296 cm(-1) is assigned to strongly hydrogen-bonded water with an H bond distance of 2.72 A. The water in agardites is better described as structured water and not as zeolitic water. Two bands at around 999 and 975 cm(-1) are assigned to OH deformation modes. Two sets of AsO symmetric stretching vibrations were found and assigned to the vibrational modes of AsO(4) and HAsO(4) units. Linear relationships between positions of infrared bands associated with bonding to the OH units and the electronegativity of the rare earth elements were derived, with correlation coefficients >0.92. These linear functions were then used to calculate the electronegativity of Eu, for which a value of 1.1808 on the Pauling scale was found.

Probing the volcanic-plutonic connection and the genesis of crystal-rich rhyolite in a deeply dissected supervolcano in the Nevada Great Basin: Source of the late Eocene Caetano Tuff

USGS Publications Warehouse

Watts, Kathryn E.; John, David A.; Colgan, Joseph P.; Henry, Christopher D.; Bindeman, Ilya N.; Schmitt, Axel K.

2016-01-01

Late Cenozoic faulting and large-magnitude extension in the Great Basin of the western USA has created locally deep windows into the upper crust, permitting direct study of volcanic and plutonic rocks within individual calderas. The Caetano caldera in north–central Nevada, formed during the mid-Tertiary ignimbrite flare-up, offers one of the best exposed and most complete records of caldera magmatism. Integrating whole-rock geochemistry, mineral chemistry, isotope geochemistry and geochronology with field studies and geologic mapping, we define the petrologic evolution of the magmatic system that sourced the >1100 km3Caetano Tuff. The intra-caldera Caetano Tuff is up to ∼5 km thick, composed of crystal-rich (30–45 vol. %), high-silica rhyolite, overlain by a smaller volume of comparably crystal-rich, low-silica rhyolite. It defies classification as either a monotonous intermediate or crystal-poor zoned rhyolite, as commonly ascribed to ignimbrite eruptions. Crystallization modeling based on the observed mineralogy and major and trace element geochemistry demonstrates that the compositional zonation can be explained by liquid–cumulate evolution in the Caetano Tuff magma chamber, with the more evolved lower Caetano Tuff consisting of extracted liquids that continued to crystallize and mix in the upper part of the chamber following segregation from a cumulate-rich, and more heterogeneous, source mush. The latter is represented in the caldera stratigraphy by the less evolved upper Caetano Tuff. Whole-rock major, trace and rare earth element geochemistry, modal mineralogy and mineral chemistry, O, Sr, Nd and Pb isotope geochemistry, sanidine Ar–Ar geochronology, and zircon U–Pb geochronology and trace element geochemistry provide robust evidence that the voluminous caldera intrusions (Carico Lake pluton and Redrock Canyon porphyry) are genetically equivalent to the least evolved Caetano Tuff and formed from magma that remained in the lower chamber after ignimbrite eruption and caldera collapse. Thus, the Caetano Tuff contradicts models for the mutually exclusive origins of voluminous volcanic and plutonic magmas in the upper crust. Crystal-scale O isotope data indicate that the Caetano Tuff is one of the most 18O-enriched rhyolites in the Great Basin (δ18Omagma = 10·2 ± 0·2‰), supporting anatexis of local metasedimentary basement crust. Metapelite xenoliths in the Carico Lake pluton and ubiquitous xenocrystic zircons in the Caetano Tuff provide constraints for the anatexis process; these data point to shallow (<15 km) dehydration melting of a protolith similar to the Proterozoic McCoy Creek Group siliciclastic sediments in eastern Nevada, projected beneath Caetano in fault-stacked shelf sediments that were thickened during Mesozoic crustal shortening. Mean zircon U–Pb ages for different stratigraphic levels of the intra-caldera Caetano Tuff are 34·2–34·5 Ma, 0·2–0·5 Myr older than the caldera sanidine 40Ar/39Ar age of 34·00 ± 0·03 Ma, documenting protracted duration of assembly and homogenization of isotopically diverse upper crustal melts, followed by crystallization and zonation to generate the Caetano Tuff magma chamber. Sanidine rims in the least evolved Caetano Tuff and in the Carico Lake pluton and Redrock Canyon porphyry have sharply zoned Ba domains that point to crystal growth during magmatic recharge events. The recharge magma is inferred to have been compositionally similar to the Caetano Tuff magma, with increased Ba resulting from remelting of Ba-rich sanidine cumulates. Mush reactivation to generate the Caetano Tuff eruption was sufficiently rapid to preserve compositional gradients in the intracaldera ignimbrite, calling into question models that predict homogeneity as a prerequisite for remobilizing crystal-rich ignimbrite magmas.

Potential Applications of Zeolite Membranes in Reaction Coupling Separation Processes

PubMed Central

Daramola, Michael O.; Aransiola, Elizabeth F.; Ojumu, Tunde V.

2012-01-01

Future production of chemicals (e.g., fine and specialty chemicals) in industry is faced with the challenge of limited material and energy resources. However, process intensification might play a significant role in alleviating this problem. A vision of process intensification through multifunctional reactors has stimulated research on membrane-based reactive separation processes, in which membrane separation and catalytic reaction occur simultaneously in one unit. These processes are rather attractive applications because they are potentially compact, less capital intensive, and have lower processing costs than traditional processes. Therefore this review discusses the progress and potential applications that have occurred in the field of zeolite membrane reactors during the last few years. The aim of this article is to update researchers in the field of process intensification and also provoke their thoughts on further research efforts to explore and exploit the potential applications of zeolite membrane reactors in industry. Further evaluation of this technology for industrial acceptability is essential in this regard. Therefore, studies such as techno-economical feasibility, optimization and scale-up are of the utmost importance.

NMR crystallography of zeolites: How far can we go without diffraction data?

PubMed

Brouwer, Darren H; Van Huizen, Jared

2018-05-10

Nuclear magnetic resonance (NMR) crystallography-an approach to structure determination that seeks to integrate solid-state NMR spectroscopy, diffraction, and computation methods-has emerged as an effective strategy to determine structures of difficult-to-characterize materials, including zeolites and related network materials. This paper explores how far it is possible to go in determining the structure of a zeolite framework from a minimal amount of input information derived only from solid-state NMR spectroscopy. It is shown that the framework structure of the fluoride-containing and tetramethylammonium-templated octadecasil clathrasil material can be solved from the 1D 29 Si NMR spectrum and a single 2D 29 Si NMR correlation spectrum alone, without the space group and unit cell parameters normally obtained from diffraction data. The resulting NMR-solved structure is in excellent agreement with the structures determined previously by diffraction methods. It is anticipated that NMR crystallography strategies like this will be useful for structure determination of other materials, which cannot be solved from diffraction methods alone. Copyright © 2018 John Wiley & Sons, Ltd.

Deep electrical investigations in the Long Valley geothermal area, California

DOE Office of Scientific and Technical Information (OSTI.GOV)

Stanley, W.D.; Jackson, D.B.; Zohdy, A.A.R.

1976-02-10

Direct current resistivity and time domain electromagnetic techniques were used to study the electrical structure of the Long Valley geothermal area. A resistivity map was compiled from 375 total field resistivity measurements. Two significant zones of low resistivity were detected, one near Casa Diablo Hot Springs and one surrounding the Cashbaugh Ranch-Whitmore Hot Springs area. These anomalies and other parts of the caldera were investigated in detail with 49 Schlumberger dc soundings and 13 transient electromagnetic soundings. An extensive conductive zone of 1- to 10-..cap omega..m resistivity was found to be the cause of the total field resistivity lows. Drillmore » hole information indicates that the shallow parts of the conductive zone in the eastern part of the caldera contain water of only 73/sup 0/C and consist of highly zeolitized tuffs and ashes in the places that were tested. A deeper zone near Whitmore Hot Springs is somewhat more promising in potential for hot water, but owing to the extensive alteration prevalent in the caldera the presence of hot water cannot be definitely assumed. The resistivity results indicate that most of the past hydrothermal activity, and probably most of the present activity, is controlled by fracture systems related to regional Sierran faulting.« less

Haneş and Valea Vinului (Romania) closed mines Acid Mine Drainages (AMDs)--actual condition and passive treatment remediation proposal.

PubMed

Măicăneanu, Andrada; Bedelean, Horea; Ardelean, Marius; Burcă, Silvia; Stanca, Maria

2013-10-01

Acid Mine Drainages (AMDs) from Haneş and Valea Vinului (Romania) closed mines were considered for characterization and treatment using a local zeolitic volcanic tuff, ZVT, (Măcicaş, Cluj County, Romania). Water samples were collected from two locations, before and after discharging point in case of Haneş mine, and on three horizons in case of Valea Vinului mine. Physico-chemical (pH, total solid, heavy metal ions concentration) analyses showed that the environment is strongly affected by these AMD discharges even if the mines were closed years ago. Iron, manganese and zinc were the main pollutants identified in Haneş mine AMD, while zinc is the one mainly present in case of Valea Vinului AMD. A batch technique (no stirring) in which the ZVT was put in contact with the AMD sample was proposed as a passive remediation technique. ZVT successfully remove heavy metal ion from AMD. According to heavy metal ion concentrations, removal efficiencies are reaching 100%, varying as follows, Fe(2+)>Zn(2+)>Mn(2+). When the ZVT was compared with two cationic resins (strong, SAR and weak acid, WAR) the following series was depicted, SAR>ZVT>WAR. Copyright © 2013 Elsevier Ltd. All rights reserved.

Sorption of As(V) on aluminosilicates treated with Fe(II) nanoparticles.

PubMed

Dousová, Barbora; Grygar, Tomás; Martaus, Alexandr; Fuitová, Lucie; Kolousek, David; Machovic, Vladimír

2006-10-15

Adsorption of arsenic on clay surfaces is important for the natural and simulated removal of arsenic species from aqueous environments. In this investigation, three samples of clay minerals (natural metakaoline, natural clinoptilolite-rich tuff, and synthetic zeolite) in both untreated and Fe-treated forms were used for the sorption of arsenate from model aqueous solution. The treatment of minerals consisted of exposing them to concentrated solution of Fe(II). Within this process the mineral surface has been laden with Fe(III) oxi(hydroxides) whose high affinity for the As(V) adsorption is well known. In all investigated systems the sorption capacity of Fe(II)-treated sorbents increased significantly in comparison to the untreated material (from about 0.5 to >20.0 mg/g, which represented more than 95% of the total As removal). The changes of Fe-bearing particles in the course of treating process and subsequent As sorption were investigated by the diffuse reflectance spectroscopy and the voltammetry of microparticles. IR spectra of treated and As(V)-saturated solids showed characteristic bands caused by Fe(III)SO(4), Fe(III)O, and AsO vibrations. In untreated As(V)-saturated solids no significant AsO vibrations were observed due to the negligible content of sorbed arsenate.

Facile synthesis of hollow zeolite microspheres through dissolution–recrystallization procedure in the presence of organosilanes

DOE Office of Scientific and Technical Information (OSTI.GOV)

Tao, Haixiang; Ren, Jiawen; Liu, Xiaohui

2013-04-15

Hollow zeolite microspheres have been hydrothermally synthesized in the presence of organosilanes via a dissolution–recrystallization procedure. In the presence of organosilanes, zeolite particles with a core/shell structure formed at the first stage of hydrothermal treatment, then the core was consumed and recrystallized into zeolite framework to form the hollow structure during the second hydrothermal process. The influence of organosilanes was discussed, and a related dissolution–recrystallization mechanism was proposed. In addition, the hollow zeolite microspheres exhibited an obvious advantage in catalytic reactions compared to conventional ZSM-5 catalysts, such as in the alkylation of toluene with benzyl chloride. - Graphical abstract: Hollowmore » zeolite spheres with aggregated zeolite nanocrystals were synthesized via a dissolution–recrystallization procedure in the presence of organosiline. Highlights: ► Hollow zeolite spheres with aggregated zeolite nanocrystals were synthesized via a dissolution–recrystallization procedure. ► Organosilane influences both the morphology and hollow structure of zeolite spheres. ► Hollow zeolite spheres showed an excellent catalytic performance in alkylation of toluene with benzyl chloride.« less

Geoengineering characterization of welded tuffs from laboratory and field investigations

DOE Office of Scientific and Technical Information (OSTI.GOV)

Zimmerman, R.M.; Nimick, F.B.; Board, M.P.

1984-12-31

Welded tuff beneath Yucca Mountain adjacent to the Nevada Test Site (NTS) is being considered for development as a high-level radioactive waste repository by the Nevada Nuclear Waste Storage Investigations (NNWSI) Project. Because access into Yucca Mountain has been limited to borehole explorations, early geoengineering materials characterizations have been derived from laboratory tests on cores from Yucca Mountain and from laboratory and field tests on welded tuffs located in G-Tunnel on the NTS. G-Tunnel contains welded tuffs that have similar properties and stress states to those at Yucca Mountain and has been the location for in situ rock mechanics testing.more » The purpose of this paper is to summarize the geoengineering material property data obtained to date and to compare appropriate laboratory and field data from G-Tunnel to findings from Yucca Mountain. Geomechanical and thermal data are provided and are augmented by limited geological and hydrological data. A comparison of results of laboratory measurements on tuffs from Yucca Mountain and G-Tunnel indicates good agreement between the bulk densities, saturations, moduli of elasticity, Poisson`s ratios, and P-wave velocities. The G-Tunnel tuff has slightly lower thermal conductivity, tensile strength, compressive strength and slightly higher matrix permeability than does the welded tuff near the proposed repository horizon at Yucca Mountain. From a laboratory-to-field scaling perspective, the modulus of deformation shows the most sensitivity to field conditions because of the presence of the joints found in the field. 14 references, 1 table.« less

Geoengineering characterization of welded tuffs from laboratory and field investigations

DOE Office of Scientific and Technical Information (OSTI.GOV)

Zimmerman, R.M.; Nimick, F.B.; Board, M.P.

1984-12-31

Welded tuff beneath Yucca Mountain adjacent to the Nevada Test Site (NTS) is being considered for development as a high-level radioactive waste repository by the Nevada Nuclear Waste Storage Investigations (NNWSI) Project. Because access into Yucca Mountain has been limited to borehole explorations, early geoengineering materials characterizations have been derived from laboratory tests on cores from Yucca Mountain and from laboratory and field tests on welded tuffs located in G-Tunnel on the NTS. G-Tunnel contains welded tuffs that have similar properties and stress states to those at Yucca Mountain and has been the location for in situ rock mechanics testing.more » The purpose of this paper is to summarize the geoengineering material property data obtained to date and to compare appropriate laboratory and field data from G-Tunnel to findings from Yucca Mountain. Geomechanical and thermal data are provided and are augmented by limited geological and hydrological data. A comparison of results of laboratory measurements on tuffs from Yucca Mountain and G-Tunnel indicates good agreement between the bulk densities, saturations, moduli of elasticity, Poisson`s ratios, and P-wave velocities. The G-Tunnel tuff has slightly lower thermal conductivity, tensile strength, compressive strength and slightly higher matrix permeability than does the welded tuff near the proposed repository horizon at Yucca Mountain. From a laboratory-to-field scaling perspective, the modulus of deformation shows the most sensitivity to field conditions because of the presence of joints found in the field. 14 refs., 1 tab.« less

Revealing Lattice Expansion of Small-Pore Zeolite Catalysts during the Methanol-to-Olefins Process Using Combined Operando X-ray Diffraction and UV-vis Spectroscopy.

PubMed

Goetze, Joris; Yarulina, Irina; Gascon, Jorge; Kapteijn, Freek; Weckhuysen, Bert M

2018-03-02

In small-pore zeolite catalysts, where the size of the pores is limited by eight-ring windows, aromatic hydrocarbon pool molecules that are formed inside the zeolite during the Methanol-to-Olefins (MTO) process cannot exit the pores and are retained inside the catalyst. Hydrocarbon species whose size is comparable to the size of the zeolite cage can cause the zeolite lattice to expand during the MTO process. In this work, the formation of retained hydrocarbon pool species during MTO at a reaction temperature of 400 °C was followed using operando UV-vis spectroscopy. During the same experiment, using operando X-ray Diffraction (XRD), the expansion of the zeolite framework was assessed, and the activity of the catalyst was measured using online gas chromatography (GC). Three different small-pore zeolite frameworks, i.e., CHA, DDR, and LEV, were compared. It was shown using operando XRD that the formation of retained aromatic species causes the zeolite lattice of all three frameworks to expand. Because of the differences in the zeolite framework dimensions, the nature of the retained hydrocarbons as measured by operando UV-vis spectroscopy is different for each of the three zeolite frameworks. Consequently, the magnitude and direction of the zeolite lattice expansion as measured by operando XRD also depends on the specific combination of the hydrocarbon species and the zeolite framework. The catalyst with the CHA framework, i.e., H-SSZ-13, showed the biggest expansion: 0.9% in the direction along the c -axis of the zeolite lattice. For all three zeolite frameworks, based on the combination of operando XRD and operando UV-vis spectroscopy, the hydrocarbon species that are likely to cause the expansion of the zeolite cages are presented; methylated naphthalene and pyrene in CHA, 1-methylnaphthalene and phenalene in DDR, and methylated benzene and naphthalene in LEV. Filling of the zeolite cages and, as a consequence, the zeolite lattice expansion causes the deactivation of these small-pore zeolite catalysts during the MTO process.

Revealing Lattice Expansion of Small-Pore Zeolite Catalysts during the Methanol-to-Olefins Process Using Combined Operando X-ray Diffraction and UV–vis Spectroscopy

PubMed Central

2018-01-01

In small-pore zeolite catalysts, where the size of the pores is limited by eight-ring windows, aromatic hydrocarbon pool molecules that are formed inside the zeolite during the Methanol-to-Olefins (MTO) process cannot exit the pores and are retained inside the catalyst. Hydrocarbon species whose size is comparable to the size of the zeolite cage can cause the zeolite lattice to expand during the MTO process. In this work, the formation of retained hydrocarbon pool species during MTO at a reaction temperature of 400 °C was followed using operando UV–vis spectroscopy. During the same experiment, using operando X-ray Diffraction (XRD), the expansion of the zeolite framework was assessed, and the activity of the catalyst was measured using online gas chromatography (GC). Three different small-pore zeolite frameworks, i.e., CHA, DDR, and LEV, were compared. It was shown using operando XRD that the formation of retained aromatic species causes the zeolite lattice of all three frameworks to expand. Because of the differences in the zeolite framework dimensions, the nature of the retained hydrocarbons as measured by operando UV–vis spectroscopy is different for each of the three zeolite frameworks. Consequently, the magnitude and direction of the zeolite lattice expansion as measured by operando XRD also depends on the specific combination of the hydrocarbon species and the zeolite framework. The catalyst with the CHA framework, i.e., H-SSZ-13, showed the biggest expansion: 0.9% in the direction along the c-axis of the zeolite lattice. For all three zeolite frameworks, based on the combination of operando XRD and operando UV–vis spectroscopy, the hydrocarbon species that are likely to cause the expansion of the zeolite cages are presented; methylated naphthalene and pyrene in CHA, 1-methylnaphthalene and phenalene in DDR, and methylated benzene and naphthalene in LEV. Filling of the zeolite cages and, as a consequence, the zeolite lattice expansion causes the deactivation of these small-pore zeolite catalysts during the MTO process. PMID:29527401

Origin of metaluminous and alkaline volcanic rocks of the Latir volcanic field, northern Rio Grande rift, New Mexico

USGS Publications Warehouse

Johnson, C.M.; Lipman, P.W.

1988-01-01

Volcanic rocks of the Latir volcanic field evolved in an open system by crystal fractionation, magma mixing, and crustal assimilation. Early high-SiO2 rhyolites (28.5 Ma) fractionated from intermediate compositionmagmas that did not reach the surface. Most precaldera lavas have intermediate-compositions, from olivine basaltic-andesite (53% SiO2) to quartz latite (67% SiO2). The precaldera intermediate-composition lavas have anomalously high Ni and MgO contents and reversely zoned hornblende and augite phenocrysts, indicating mixing between primitive basalts and fractionated magmas. Isotopic data indicate that all of the intermediate-composition rocks studied contain large crustal components, although xenocrysts are found only in one unit. Inception of alkaline magmatism (alkalic dacite to high-SiO2 peralkaline rhyolite) correlates with, initiation of regional extension approximately 26 Ma ago. The Questa caldera formed 26.5 Ma ago upon eruption of the >500 km3 high-SiO2 peralkaline Amalia Tuff. Phenocryst compositions preserved in the cogenetic peralkaline granite suggest that the Amalia Tuff magma initially formed from a trace element-enriched, high-alkali metaluminous magma; isotopic data suggest that the parental magmas contain a large crustal component. Degassing of water- and halogen-rich alkali basalts may have provided sufficient volatile transport of alkalis and other elements into the overlying silicic magma chamber to drive the Amalia Tuff magma to peralkaline compositions. Trace element variations within the Amalia Tuff itself may be explained solely by 75% crystal fractionation of the observed phenocrysts. Crystal settling, however, is inconsistent with mineralogical variations in the tuff, and crystallization is thought to have occurred at a level below that tapped by the eruption. Spatially associated Miocene (15-11 Ma) lavas did not assimilate large amounts of crust or mix with primitive basaltic magmas. Both mixing and crustal assimilation processes appear to require development of relatively large magma chambers in the crust that are sustained by large basalt fluxes from the mantle. The lack of extensive crustal contamination and mixing in the Miocene lavas may be related to a decreased basalt flux or initiation of blockfaulting that prevented pooling of basaltic magma in the crust. ?? 1988 Springer-Verlag.

Histamine-binding capacities of different natural zeolites: a comparative study.

PubMed

Selvam, Thangaraj; Schwieger, Wilhelm; Dathe, Wilfried

2018-06-07

Two different natural zeolites from Cuba and Mexico, which are already being used as contemporaneous drugs or dietary supplements in Germany and Mexico, respectively, are applied in a comparative study of their histamine-binding capacities as a function of their particle sizes. The zeolites are characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM) and N 2 -sorption measurements (BET surface areas). The Cuban zeolite contains clinoptilolite and mordenite as major phases (78% zeolite), whereas the Mexican one contains only clinoptilolite (65% zeolite). Both zeolites are apparently free from fibrous materials according to SEM. Both zeolites adsorb significant amount of histamine under the experimental conditions. Nevertheless, the results showed that the histamine-binding capacity of the Cuban zeolite is higher than the Mexican one and the smaller the particle size of zeolite, the higher the histamine-binding capacity. This difference could be due to the variation in their mineralogical compositions resulting in varied BET surface areas. Thus, the high histamine-binding capacities of Cuban zeolites seem to be due at least partly to the presence of the large-pore zeolite mordenite, providing high total pore volumes, which will be discussed in detail. For the first time, we have shown that the mineralogical compositions of natural zeolites and their particle sizes play a key role in binding histamine, which is one of the most important regulators in human physiology.

Integrated synthesis of zeolites 4A and Na-P1 using coal fly ash for application in the formulation of detergents and swine wastewater treatment.

PubMed

Cardoso, Ariela M; Horn, Martha B; Ferret, Lizete S; Azevedo, Carla M N; Pires, Marçal

2015-04-28

Several researchers have reported zeolite synthesis using coal ash for a wide range of applications. However, little attention has been given to green processes, including moderate synthesis conditions, using waste as raw material and effluent reuse or reduction. In this study, Brazilian coal fly ashes were used for integrated synthesis of zeolites 4A and Na-P1 by two different routes and under moderate operating conditions (temperature and pressure). Both procedures produced zeolites with similar conversions (zeolite 4A at 82% purity and zeolite Na-P1 at 57-61%) and high CEC values (zeolites 4A: 4.5meqCa(2+)g(-1) and zeolites Na-P1: 2.6-2.8meqNH4(+)g(-1)). However, process 1 generated less effluent for the zeolite mass produced (7mLg(-1)), with low residual Si and Al levels and 74% of the Si available in the coal fly ash incorporated into the zeolite, while only 55% is used in process 2. For use as a builder in detergents, synthetic zeolite 4A exhibited conformity parameters equal to or greater than those of the commercial zeolite adopted as reference. Treatment of swine wastewater with zeolite Na-P1 resulted in a high removal capacity for total ammoniacal nitrogen (31mgg(-1)). Copyright © 2015 Elsevier B.V. All rights reserved.

UTILITY OF ZEOLITES IN ARSENIC REMOVAL FROM WATER

EPA Science Inventory

Zeolites are well known for their ion exchange and adsorption properties. So far the cation exchanger properties of zeolites have been extensively studied and utilized. The anion exchanger properties of zeolites are less studied. Zeolite Faujasite Y has been used to remove arseni...

The Onset of the Sturtian Snowball Earth: New Geochronology and Chemostratigraphy from the Tambien Group of Ethiopia

NASA Astrophysics Data System (ADS)

Park, Y.; MacLennan, S. A.; Swanson-Hysell, N.; Maloof, A. C.; Schoene, B.; Alene, M.; Tremblay, M. M.; Anttila, E.; Haileab, B.

2016-12-01

The Snowball Earth hypothesis proposes that the onset of global glaciation was a rapid event, particularly at low-latitudes, due to a runaway ice-albedo instability in the climate system. Currently, the Neoproterozoic Sturtian Snowball Earth Glaciation is constrained to have been ongoing at low-latitudes in present day NW Canada at 716.47 ± 0.24 Ma based on a U-Pb date from a tuff within glacial diamictite (Macdonald et al., 2010). A date from a rhyolite underlying this diamicitite of 717.43 ± 0.14 Ma has been inferred to precede the glaciation, although this age is not a strict maximum for the initiation of the snowball Earth since evidence of glaciation may have been obscured in volcanic units. The Tonian-Cryogenian Tambien Group of northern Ethiopia is a mixed carbonate-siliciclastic sequence deposited in an arc proximal basin that conformably culminates in diamictite associated with the Sturtian Glaciation. This study exploits the presence of tuffs suitable for high precision U-Pb zircon geochronology interbedded with recently discovered exposures of the transition into the snowball Earth. Dates from tuffs stratigraphically <100 m below massive diamictite enable a test of synchronicity for the initiation of the Sturtian Glaciation when compared with data from NW Canada and S China. Furthermore, tuffs in the proximity of the chemostratigraphically defined Islay negative δ13C anomaly give the opportunity to develop new U-Pb dates to test the prediction from Re-Os dating of black shales in NW Canada that the Islay significantly predates the Sturtian ice age, decoupling the sharpest negative downturns in inorganic δ13C values from glacial initiation. These data also augment and temporally constrain the pre-glacial 87Sr/86Sr curve, informing ongoing modeling efforts of global weathering and seawater chemistry as they relate to hypotheses of the role of large igneous province emplacement and paleogeography in the initiation of Snowball Earth glaciation.

2.8-Ma ash-flow caldera at Chegem River in the northern Caucasus Mountains (Russia), contemporaneous granites, and associated ore deposits

USGS Publications Warehouse

Lipman, P.W.; Bogatikov, O.A.; Tsvetkov, A.A.; Gazis, C.; Gurbanov, A.G.; Hon, K.; Koronovsky, N.V.; Kovalenko, V.I.; Marchev, P.

1993-01-01

Diverse latest Pliocene volcanic and plutonic rocks in the north-central Caucasus Mountains of southern Russia are newly interpreted as components of a large caldera system that erupted a compositionally zoned rhyolite-dacite ash-flow sheet at 2.83 ?? 0.02 Ma (sanidine and biotite 40Ar/39Ar). Despite its location within a cratonic collision zone, the Chegem system is structurally and petrologically similar to typical calderas of continental-margin volcanic arcs. Erosional remnants of the outflow Chegem Tuff sheet extend at least 50 km north from the source caldera in the upper Chegem River. These outflow remnants were previously interpreted by others as erupted from several local vents, but petrologic similarities indicate a common origin and correlation with thick intracaldera Chegem Tuff. The 11 ?? 15 km caldera and associated intrusions are superbly exposed over a vertical range of 2,300 m in deep canyons above treeline (elev. to 3,800 m). Densely welded intracaldera Chegem Tuff, previously described by others as a rhyolite lava plateau, forms a single cooling unit, is > 2 km thick, and contains large slide blocks from the caldera walls. Caldera subsidence was accommodated along several concentric ring fractures. No prevolcanic floor is exposed within the central core of the caldera. The caldera-filling tuff is overlain by andesitic lavas and cut by a 2.84 ?? 0.03-Ma porphyritic granodiorite intrusion that has a cooling age analytically indistinguishable from that of the tuffs. The Eldjurta Granite, a pluton exposed low in the next large canyon (Baksan River) 10 km to the northwest of the caldera, yields variable K-feldspar and biotite ages (2.8 to 1.0 Ma) through a 5-km vertical range in surface and drill-hole samples. These variable dates appear to record a prolonged complex cooling history within upper parts of another caldera-related pluton. Major W-Mo ore deposits at the Tirniauz mine are hosted in skarns and hornfels along the roof of the Eldjurta Granite, and associated aplitic phases have textural features of Climax-type molybdenite porphyries in the western USA. Similar 40Ar/39Ar ages, mineral chemistry, and bulk-rock compositions indicate that the Chegem Tuff, intracaldera intrusion, and Eldjurta Granite are all parts of a large magmatic system that broadly resembles the middle Tertiary Questa caldera system and associated Mo deposits in northern New Mexico, USA. Because of their young age and superb three-dimensional exposures, rocks of the Chegem-Tirniauz region offer exceptional opportunities for detailed study of caldera structures, compositional gradients in volcanic rocks relative to cogenetic granites, and the thermal and fluid-flow history of a large young upper-crustal magmatic system. ?? 1993.

Tectonic Setting and Bimodal Magmatic Evolution of Eocene Volcanic Rocks of the Bijgerd-Kuh-e Kharchin area, Uromieh-Dokhtar Zone, Iran

NASA Astrophysics Data System (ADS)

Davarpanah, A.; Khalatbari-Jafari, M.; Babaie, H. A.; Krogstad, E. J.; Mobasher, K.; La Tour, T. E.; Deocampo, D. M.

2008-12-01

Geochemical composition and texture of the Middle and Late Eocene volcanic, volcaniclastic, and volcanic- sedimentary rocks in the Bijgerd-Kuh-e Kharchin area, northwest of Saveh, provide significant geochemical and geological clues for the tectonic and magmatic evolution of the Uromieh-Dokhtar volcanic-plutonic zone of Iran. The Middle Eocene volcanic rocks have an intermediate composition and include green tuff and tuffaceous sandstone with intercalated sandstone, sandy tuff, and shale. The shale has lenses of nummulite- bearing limestone with a Middle Eocene detrital age. The time between the Middle and Late Eocene volcanic activities in this area is marked by the presence of andesite and rhyolitic tuff. The Late Eocene succession is distinguished by the presence of four alternating levels (horizons) of intermediate lava and ignimbrite which we designate as Eig. The ignimbrites of the Eig sequence have a rhyolitic composition and include ignimbrite- breccia, ignimbrite-tuff, and ignimbrite-lava pairs. The volume of the felsic volcanic rocks in this sequence far exceeds that of the intermediate rocks, which makes it unlikely that they evolved through the magmatic differentiation of a basaltic magma. The presence of the nummulite-bearing limestone lenses, and sandstone and conglomerate interbeds between the ignimbrites, suggests a shallow marine environment for the pyroclastic deposition and probably the eruptions. The tuff and siltstone of the Est unit that sits above the first ignimbrite may represent deep water, Late Eocene deposit. Oligo-Miocene limestone of the Qom Formation unconformably overlies the uppermost Late Eocene ignimbrite. Washings from red marls give microfossils with Late Eocene age for the Eig sequence, which is synchronous with other paleontological evidence that puts the peak volcanic activity as Late Eocene in the Bijgerd-Kuh-e Kharchin area. Field and petrographic evidence for magma mixing/mingling is given by the presence of mafic- intermediate enclaves in the ignimbrite, hybrid breccias with felsic and mafic clasts, felsic pseudo-flames filled with intermediate lava, heterogeneity in the ignimbrite texture, and sieve texture and oscillatory zoning of plagioclase and opacitization of olivine in the intermediate lava. Geochemical analyses of the major and trace elements (including the REE) and rock texture and assemblages indicate the bimodal magmatic characteristics of the mafic-intermediate lavas and ignimbrites. The tuff and the breccia show a hybrid elemental distribution between those of rhyolite and basalt. The ignimbrites show more enriched compositions than those of the mafic and intermediate rocks on the chondrite-normalized trace element distribution diagram. The higher enrichment of the LREE in the ignimbrites may be due to a crustal contribution. The primitive mantle-normalized elemental distributions show a distinct depletion of Nb and Ti, which suggests a subduction-related volcanism during Eocene.

Oxygen isotopic and geochemical evidence for a short-lived, high-temperature hydrothermal event in the Chegem caldera, Caucasus Mountains, Russia

USGS Publications Warehouse

Gazis, C.; Taylor, H.P.; Hon, K.; Tsvetkov, A.

1996-01-01

Within the 2.8 Ma Chegem ash-flow caldera (11 ?? 15 km), a single cooling unit of rhyolitic to dacitic welded tuff more than 2 km thick is exposed in deep valleys incised during recent rapid uplift of the Caucasus Mountains. The intracaldera tuff is mineralogically fresh and unaltered, and is overlain by andesite lavas and cut by a resurgent granodiorite intrusion. Major- and trace-element compositions for a 1405-m stratigraphic section of intracaldera tuff display trends of upwardly increasing Na2O, CaO, Al2O3, total Fe, MgO, TiO2, Sr and Zr and decreasing SiO2, K2O and Rb. This mafic-upward zoning (from 76.1 to 69.9% SiO2) reflects an inverted view of the upper part of the source magma chamber. Oxygen isotope studies of 35 samples from this 1405-m section define a striking profile with "normal" igneous ??18O values (+7.0 to +8.5) in the lower 600 m of tuff, much lower ??18O values (-4.0 to +4.3) in a 700-m zone above that and a shift to high ??18O values (+4.4 to -10.9) in the upper 100 m of caldera-fill exposure. Data from two other partial stratigraphic sections indicate that these oxygen isotope systematics are probably a caldera-wide phenomenon. Quartz and feldspar phenocrysts everywhere have "normal" igneous ??18O values of about +8.5 and +7.5, respectively, whereas groundmass and glass ??18O values range from -7.7 to +12.3. Consequently, the ??18O values of coexisting feldspar, groundmass and glass form a steep array in a plot of ??feldspar vs. ??groundmass/glass. Such pronounced disequilibrium between coexisting feldspar and groundmass or glass has never before been observed on this scale. It requires a hydrothermal event involving large amounts of low-18O H2O at sufficiently high temperatures and short enough time (tens of years or less) that glass exchanges thoroughly but feldspar does not. The most likely process responsible for the O depletions at Chegem is a very high temperature (500-600??C), short-lived, vigorous meteoric-hydrothermal event that was focused within the upper 750 m of intracaldera tuff. Mass balance calculations indicate fluid fluxes of = 6 ?? 10-6 mol cm-2 s-1. We believe that the closest historical analogue to this Chegem hydrothermal event is the situation observed in the Valley of Ten Thousand Smokes (Alaska, USA), where hundreds of steam fumaroles with measured temperatures as high as 645??C persisted for 10 to 15 years in the much smaller welded ash-flow tuff sheet (??? 200 m thick) produced by the 1912 Katmai eruption.

Alkaline hydrothermal conversion of fly ash filtrates into zeolites 2: utilization in wastewater treatment.

PubMed

Somerset, Vernon; Petrik, Leslie; Iwuoha, Emmanuel

2005-01-01

Filtrates were collected using a codisposal reaction wherein fly ash was reacted with acid mine drainage. These codisposal filtrates were then analyzed by X-ray Fluorescence spectrometry for quantitative determination of the SiO2 and Al2O3 content. Alkaline hydrothermal zeolite synthesis was then applied to the filtrates to convert the fly ash material into zeolites. The zeolites formed under the experimental conditions were faujasite, sodalite, and zeolite A. The use of the fly ash-derived zeolites and a commercial zeolite was explored in wastewater decontamination experiments as it was applied to acid mine drainage in different dosages. The concentrations of Ni, Zn, Cd, As, and Pb metal ions in the treated wastewater were investigated. The results of the treatment of the acid mine drainage with the prepared fly ash zeolites showed that the concentrations of Ni, Zn, Cd, and Hg were decreased as the zeolite dosages of the fly ash zeolite (FAZ1) increased.

Tailored zeolites for the removal of metal oxyanions: overcoming intrinsic limitations of zeolites.

PubMed

Figueiredo, Hugo; Quintelas, Cristina

2014-06-15

This review aims to present a global view of the efforts conducted to convert zeolites into efficient supports for the removal of heavy metal oxyanions. Despite lacking affinity for these species, due to inherent charge repulsion between zeolite framework and anionic species, zeolites have still received considerable attention from the scientific community, since their versatility allowed tailoring them to answer specific requirements. Different processes for the removal and recovery of toxic metals based on zeolites have been presented. These processes resort to modification of the zeolite surface to allow direct adsorption of oxyanions, or by combination with reducing agents for oxyanions that allow ion-exchange with the converted species by the zeolite itself. In order to testify zeolite versatility, as well as covering the wide array of physicochemical constraints that oxyanions offer, chromium and arsenic oxyanions were selected as model compounds for a review of treatment/remediation strategies, based on zeolite modification. Copyright © 2014 Elsevier B.V. All rights reserved.

Natural zeolite reactivity towards ozone: the role of compensating cations.

PubMed

Valdés, Héctor; Alejandro, Serguei; Zaror, Claudio A

2012-08-15

Among indoor pollutants, ozone is recognised to pose a threat to human health. Recently, low cost natural zeolites have been applied as alternative materials for ozone abatement. In this work, the effect of compensating cation content of natural zeolite on ozone removal is studied. A Chilean natural zeolite is used here as starting material. The amount of compensating cations in the zeolite framework was modified by ion exchange using an ammonium sulphate solution (0.1 mol L(-1)). Characterisation of natural and modified zeolites were performed by X-ray powder diffraction (XRD), nitrogen adsorption at 77K, elemental analysis, X-ray fluorescence (XRF), thermogravimetric analysis coupled with mass spectroscopy (TGA-MS), and temperature-programmed desorption of ammonia (NH(3)-TPD). Ozone adsorption and/or decomposition on natural and modified zeolites were studied by diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). Results show that the zeolite compensating cation content affects ozone interaction with zeolite active sites. Ammonium ion-exchange treatments followed by thermal out-gassing at 823 K, reduces ozone diffusion resistance inside the zeolite framework, increasing ozone abatement on zeolite surface active sites. Weak and strong Lewis acid sites of zeolite surface are identified here as the main active sites responsible of ozone removal. Copyright © 2012 Elsevier B.V. All rights reserved.

Selective adsorption of thiophene and 1-benzothiophene on metal-ion-exchanged zeolites in organic medium.

PubMed

Xue, Mei; Chitrakar, Ramesh; Sakane, Kohji; Hirotsu, Takahiro; Ooi, Kenta; Yoshimura, Yuji; Feng, Qi; Sumida, Naoto

2005-05-15

Adsorption of the organic sulfur compounds thiophene (TP) and 1-benzothiophene (1-BTP) in an organic model solution of hydrodesulfurizated gasoline (heptane with 1 wt% toluene and 0.156 mM (5 ppmw as sulfur) TP or 1-BTP) was studied by a batch method at 80 degrees C using metal-ion-exchanged Y-zeolites. Although NaY-zeolite or its acid-treated material rarely adsorbed the organic sulfur compounds, NaY-zeolites exchanged with Ag+, Cu2+, and Ce3+ ions and NH(4)Y-zeolites exchanged with Ce3+ ions showed markedly high adsorptive capacities for TP and 1-BTP. The sulfur uptake increased in the order CuY-zeolite(Na)

Solvent-Free Synthesis of Zeolites: Mechanism and Utility.

PubMed

Wu, Qinming; Meng, Xiangju; Gao, Xionghou; Xiao, Feng-Shou

2018-05-08

Zeolites have been extensively studied for years in different areas of chemical industry, such as shape selective catalysis, ion-exchange, and gas adsorption and separation. Generally, zeolites are prepared from solvothermal synthesis in the presence of a large amounts of solvents such as water and alcohols in sealed autoclaves under autogenous pressure. Water has been regarded as essential to synthesize zeolites for fast mass transfer of reactants, but it occupies a large space in autoclaves, which greatly reduces the yield of zeolite products. Furthermore, polluted wastes and relatively high pressure due to the presence of water solvent in the synthesis also leads to environmental and safety issues. Recently, inspired by great benefits of solvent-free synthesis, including the environmental concerns, energy consumption, safety, and economic cost, researchers continually challenge the rationale of the solvent and reconsider the age-old question "Do we actually need solvents at all in zeolite synthesis?" In this Account, we briefly summarize our efforts to rationally synthesize zeolites via a solvent-free route. Our research demonstrates that a series of silica, aluminosilicate, and aluminophosphate-based zeolites can be successfully prepared by mixing, grinding, and heating starting solid materials under solvent-free conditions. Combining an organotemplate-free synthesis with a solvent-free approach maximizes the advantages resulting in a more sustainable synthetic route, which avoids using toxic and costly organic templates and the formation of harmful gases by calcination of organic templates at high temperature. Furthermore, new insights into the solvent-free crystallization process of zeolites have been provided by modern techniques such as NMR and UV-Raman spectroscopy, which should be helpful in designing new zeolite structures and developing novel routes for synthesis of zeolites. The role of water and the vital intermediates during the crystallization of zeolites have been proposed and verified. In addition to a significant reduction in liquid wastes and a remarkable increase in zeolite yields, the solvent-free synthesis of zeolites exhibits more unprecedented benefits, including (i) the formation of hierarchical micro-, meso-, and macrostructures, which benefit the mass transfer in the reactions, (ii) rapid synthesis at higher temperatures, which greatly improve the space-time yields of zeolites, and (iii) construction of a novel catalytic system for encapsulation of metal nanoparticles and metal oxide particles within zeolite crystals synergistically combining the advantages of catalytic metal nanoparticles and metal oxide particles (high activity) and zeolites (shape selectivity). We believe that the concept of "solvent-free synthesis of zeolites" would open a door for deep understanding of zeolite crystallization and the design of efficient zeolitic catalysts.

Geologic map of the Paintbrush Canyon Area, Yucca Mountain, Nevada

DOE Office of Scientific and Technical Information (OSTI.GOV)

Dickerson, R.P.; Drake, R.M. II

This geologic map is produced to support site characterization studies of Yucca Mountain, Nevada, site of a potential nuclear waste storage facility. The area encompassed by this map lies between Yucca Wash and Fortymile Canyon, northeast of Yucca Mountain. It is on the southern flank of the Timber Mountain caldera complex within the southwest Nevada volcanic field. Miocene tuffs and lavas of the Calico Hills Formation, the Paintbrush Group, and the Timber Mountain Group crop out in the area of this map. The source vents of the tuff cones and lava domes commonly are located beneath the thickest deposits ofmore » pyroclastic ejecta and lava flows. The rocks within the mapped area have been deformed by north- and northwest-striking, dominantly west-dipping normal faults and a few east-dipping normal faults. Faults commonly are characterized by well developed fault scarps, thick breccia zones, and hanging-wall grabens. Latest movement as preserved by slickensides on west-dipping fault scarps is oblique down towards the southwest. Two of these faults, the Paintbrush Canyon fault and the Bow Ridge fault, are major block-bounding faults here and to the south at Yucca Mountain. Offset of stratigraphic units across faults indicates that faulting occurred throughout the time these volcanic units were deposited.« less

Geologic map of the Puye Quadrangle, Los Alamos, Rio Arriba, Sandoval, and Santa Fe Counties, New Mexico

USGS Publications Warehouse

Dethier, David P.

2003-01-01

The Puye quadrangle covers an area on the eastern flank of the Jemez Mountains, north of Los Alamos and west of Espanola, New Mexico. Most of the quadrangle consists of a dissected plateau that was formed on the resistant caprock of the Bandelier Tuff, which was erupted from the Valles caldera approximately 1 to 2 million years ago. Within the canyons of the east-flowing streams that eroded this volcanic tableland, Miocene and Pliocene fluvial deposits of the Puye Formation and Santa Fe Group are exposed beneath the Bandelier Tuff. These older units preserve sand and gravel that were deposited by streams and debris flows flowing from source areas located mostly north and northeast of the Puye quadrangle. The landscape of the southeastern part of the quadrangle is dominated by the valley of the modern Rio Grande, and by remnants of piedmont-slope and river-terrace deposits that formed during various stages of incision of the Rio Grande drainage on the landscape. Landslide deposits are common along the steep canyon walls where broad tracts of the massive caprock units have slumped toward the canyons on zones of weakness in underlying strata, particularly on silt/clay-rich lacustrine beds within the Puye Formation.

Phreatomagmatic eruptions through unconsolidated coastal plain sequences, Maungataketake, Auckland Volcanic Field (New Zealand)

NASA Astrophysics Data System (ADS)

Agustín-Flores, Javier; Németh, Károly; Cronin, Shane J.; Lindsay, Jan M.; Kereszturi, Gábor; Brand, Brittany D.; Smith, Ian E. M.

2014-04-01

Maungataketake is a monogenetic basaltic volcano formed at ~ 85-89 ka in the southern part of the Auckland Volcanic Field (AVF), New Zealand. It comprises a basal 1100-m diameter tuff ring, with a central scoria/spatter cone and lava flows. The tuff ring was formed under hydrogeological and geographic conditions very similar to the present. The tuff records numerous density stratified, wet base surges that radiated outward up to 1 km, decelerating rapidly and becoming less turbulent with distance. The pyroclastic units dominantly comprise fine-grained expelled grains from various sedimentary deposits beneath the volcano mixed with a minor component of juvenile pyroclasts (~ 35 vol.%). Subtle lateral changes relate to deceleration with distance and vertical transformations are minor, pointing to stable explosion depths and conditions, with gradual transitions between units and no evidence for eruptive pauses. This volcano formed within and on ~ 60 m-thick Plio/Pleistocene, poorly consolidated, highly permeable shelly sands and silts (Kaawa Formation) capped by near-impermeable, water-saturated muds (Tauranga Group). These sediments rest on moderately consolidated Miocene-aged permeable turbiditic sandstones and siltstones (Waitemata Group). Magma-water fuelled thermohydraulic explosions remained in the shallow sedimentary layers, excavating fine-grained sediments without brittle fragmentation required. On the whole, the resulting cool, wet pyroclastic density currents were of low energy. The unconsolidated shallow sediments deformed to accommodate rapidly rising magma, leading to development of complex sill-like bodies and a range of magma-water contact conditions at any time. The weak saturated sediments were also readily liquefied to provide an enduring supply of water and fine sediment to the explosion loci. Changes in magma flux and/or subsequent stabilisation of the conduit area by a lava ring-barrier led to ensuing Strombolian and fire-fountaining eruption phases. Future eruptions in littoral environments around Auckland are likely to be of this type, producing base surges that rapidly decrease in energy over short runout distances (~ 1 km).

Hydrogeologic and hydrochemical framework, south-central Great Basin, Nevada-California, with special reference to the Nevada Test Site

DOE Office of Scientific and Technical Information (OSTI.GOV)

Winograd, I.J.; Thordarson, W.

Intensely fractured Precambrian and Paleozoic carbonate and clastic rocks and block-faulted Cenozoic volcanic and sedimentary strata in the Nevada Test Site are divided into 10 hydrogeologic units. Three of these--the lower clastic aquitard, the lower carbonate aquifer, and the tuff aquitard--control the regional movement of ground water. The coefficients of fracture transmissiblity of these rocks are, respectively, less than 1,000, 1,000 to 900,000, and less than 200 gallons per day per foot; interstitial permeability is negligible. Solution caverns are locally present in the carbonate aquifer, but regional movement of water is controlled by variations in fracture transmissibility and by structuralmore » juxtaposition of the aquifer and the lower clastic aquitard. Water circulates freely to depths of at least 1,500 feet beneath the top of the aquifer and up to 4,200 feet below land surface. Synthesis of hydrogeologic, hydrochemical, and isotopic data suggests that an area of at least 4,500 square miles (including 10 intermontane valleys) is hydraulically integrated into one ground-water basin, the Ash Meadows basin, by interbasin movement of ground water through the widespread carbonate aquifer. Discharge from this basin--a minimum of about 17,000 acre-feet annually--occurs along a fault-controlled spring line at Ash Meadows in east-central Amargosa Desert. Intrabasin movement of water between Cenozoic aquifers and the lower carbonate aquifer is controlled by the tuff aquitard, the basal Cenozoic hydrogeologic unit. Such movement significantly influences the chemistry of water in the carbonate aquifer. Ground-water velocity through the tuff aquitard in Yucca Flat is less than 1 foot per year. Velocity through the lower carbonate aquifer ranges from an estimated 0.02 to 200 feet per day, depending upon geographic position within the flow system.Within the Nevada Test Site, ground water moves southward and southwestward toward Ash Meadows.« less

Oxygen and hydrogen isotope geochemistry of zeolites

NASA Technical Reports Server (NTRS)

Karlsson, Haraldur R.; Clayton, Robert N.

1990-01-01

Oxygen and hydrogen isotope ratios for natural samples of the zeolites analcime, chabazite, clinoptilolite, laumontite, mordenite, and natrolite have been obtained. The zeolite samples were classified into sedimentary, hydrothermal, and igneous groups. The ratios for each species of zeolite are reported. The results are used to discuss the origin of channel water, the role of zeolites in water-rock interaction, and the possibility that a calibrated zeolite could be used as a low-temperature geothermometer.

Effect of Annealing Temperature on Broad Luminescence of Silver-Exchanged Zeolites Y and A

NASA Astrophysics Data System (ADS)

Gui, Sa Chu Rong; Lin, H.; Bao, W.; Wang, W.

2018-05-01

The annealing temperature dependence of luminescence properties of silver (Ag)-exchanged zeolites Y and A was studied. It was found that the absorbance and excitation/emission bands are strongly affected by the thermal treatments. With increase in annealing temperature, the absorbance of Ag in zeolite Y increases at first and then decreases. However, the position of the excitation/emission band in zeolite Y was found to be insensitive to the annealing temperature. In contrast, the excitation/emission bands in zeolite A are particularly sensitive to the annealing temperature. The difference of such temperature dependence in zeolites Y and A may be due to the different microporous structure of the two minerals. Moreover, the fact that this dependence is not observed in Ag-exchanged zeolite Y is likely to be due to the difficulty in dehydration of zeolite Y in air or due to the weak Ag+-Ag+ interaction in zeolite Y.

Catalytic Fast Pyrolysis of Cellulose Using Nano Zeolite and Zeolite/Matrix Catalysts in a GC/Micro-Pyrolyzer.

PubMed

Lee, Kyong-Hwan

2016-05-01

Cellulose, as a model compound of biomass, was catalyzed over zeolite (HY,.HZSM-5) and zeolite/matrix (HY/Clay, HM/Clay) in a GC/micro-pyrolyzer at 500 degrees C, to produce the valuable products. The catalysts used were pure zeolite and zeolite/matrix including 20 wt% matrix content, which were prepared into different particle sizes (average size; 0.1 mm, 1.6 mm) to study the effect of the particle size of the catalyst for the distribution of product yields. Catalytic pyrolysis had much more volatile products as light components and less content of sugars than pyrolysis only. This phenomenon was strongly influenced by the particle size of the catalyst in catalytic fast pyrolysis. Also, in zeolite and zeolite/matrix catalysts the zeolite type gave the dominant impact on the distribution of product yields.

Enhanced chromium adsorption capacity via plasma modification of natural zeolites

NASA Astrophysics Data System (ADS)

Cagomoc, Charisse Marie D.; Vasquez, Magdaleno R., Jr.

2017-01-01

Natural zeolites such as mordenite are excellent adsorbents for heavy metals. To enhance the adsorption capacity of zeolite, sodium-exchanged samples were irradiated with 13.56 MHz capacitively coupled radio frequency (RF) argon gas discharge. Hexavalent chromium [Cr(VI)] was used as the test heavy metal. Pristine and plasma-treated zeolite samples were soaked in 50 mg/L Cr solution and the amount of adsorbed Cr(VI) on the zeolites was calculated at predetermined time intervals. Compared with untreated zeolite samples, initial Cr(VI) uptake was 70% higher for plasma-treated zeolite granules (50 W 30 min) after 1 h of soaking. After 24 h, all plasma-treated zeolites showed increased Cr(VI) uptake. For a 2- to 4-month period, Cr(VI) uptake increased about 130% compared with untreated zeolite granules. X-ray diffraction analyses between untreated and treated zeolite samples revealed no major difference in terms of its crystal structure. However, for plasma-treated samples, an increase in the number of surface defects was observed from scanning electron microscopy images. This increase in the number of surface defects induced by plasma exposure played a crucial role in increasing the number of active sorption sites on the zeolite surface.

Correlation of ash-flow tuffs.

USGS Publications Warehouse

Hildreth, W.; Mahood, G.

1985-01-01

Discrimination and correlation of ash-flow sheets is important in structurally complex, long-lived volcanic fields where such sheets provide the best keys to the regional stratigraphic framework. Three-dimensional complexities resulting from pulsatory eruptions, sectorial emplacement, mechanical sorting during outflow, thermal and compositional zoning of magmas, the physical zoning of cooling units, and structural and erosional disruption can make such correlation and discrimination difficult. When lithologic, magnetic, petrographic, chemical, and isotopic criteria for correlating ash-flow sheets are critically evaluated, many problems and pitfalls can be identified. Distinctive phenocrysts, pumice clasts, and lithic fragments are among the more reliable criteria, as are high-precision K-Ar ages and thermal remanent magnetization (TRM) directions in unaltered welded tuff. Chemical correlation methods should rely principally upon welded or nonwelded pumice blocks, not upon the ash-flow matrix, which is subject to fractionation, mixing, and contamination during emplacement. Compositional zoning of most large sheets requires that many samples be analyzed before phenocryst, glass or whole-rock chemical trends can be used confidently as correlation criteria.-Authors

Using natural clinoptilolite zeolite as an amendment in vermicomposting of food waste.

PubMed

Zarrabi, Mansur; Mohammadi, Ali Akbar; Al-Musawi, Tariq J; Najafi Saleh, Hossein

2018-06-02

The effect of adding different proportions of natural clinoptilolite zeolite (5 and 10%) to food waste vermicomposting was investigated by assessing the physicochemical characteristics, worms' growth, and maturation time of finished vermicompost in comparison with the vermicompost prepared with no amendment (control). Vermicomposting was performed in 18 plastic containers for 70 days. The experimental results showed that the carbon-to-nitrogen (C/N) ratios were 15.85, 10.75, and 8.94 for 5 and 10% zeolite concentration and control after 70 days, respectively. The addition of zeolite could facilitate organic matter degradation and increase the total nitrogen content by adsorption of ammonium ions. Increasing the proportion of zeolite from 0% (control) to 10% decreased the ammonia escape by 25% in the final vermicompost. The natural zeolite significantly reduced the electrical conductivity (EC). At the end of the process, salinity uptake efficiency was 39.23% for 5% zeolite treatment and 45.23% for 10% zeolite treatment. The pH values at 5 and 10% zeolite-amended treatments were 7.31 and 7.57, respectively, in comparison to 7.10 in the control. The maturation time at the end of vermicomposting decreased with increasing zeolite concentration. The vermicompost containing 5 and 10% zeolite matured in 49 and 42 days, respectively, in comparison to 56 days for the control. With the use of an initial ten immature Eisenia fetida worms, the number of mature worms in the 10% zeolite treatment was 26 more than that in the 5% zeolite treatment (21 worms) and 9 more than that in the control treatment (17 worms). Significantly, natural zeolite showed a beneficial effect on the characteristics of the end-product when used in the vermicomposting of food waste.

Investigating the Influence of Temperature on the Kaolinite-Base Synthesis of Zeolite and Urease Immobilization for the Potential Fabrication of Electrochemical Urea Biosensors.

PubMed

Anderson, David Ebo; Balapangu, Srinivasan; Fleischer, Heidimarie N A; Viade, Ruth A; Krampa, Francis D; Kanyong, Prosper; Awandare, Gordon A; Tiburu, Elvis K

2017-08-08

Temperature-dependent zeolite synthesis has revealed a unique surface morphology, surface area and pore size which influence the immobilization of urease on gold electrode supports for biosensor fabrication. XRD characterization has identified zeolite X (Na) at all crystallization temperatures tested. However, N₂ adsorption and desorption results showed a pore size and pore volume of zeolite X (Na) 60 °C, zeolite X (Na) 70 °C and zeolite X (Na) 90 °C to range from 1.92 nm to 2.45 nm and 0.012 cm³/g to 0.061 cm³/g, respectively, with no significant differences. The specific surface area of zeolite X (Na) at 60, 70 and 90 °C was 64 m²/g, 67 m²/g and 113 m²/g, respectively. The pore size, specific surface area and pore volumes of zeolite X (Na) 80 °C and zeolite X (Na) 100 °C were dramatically increased to 4.21 nm, 295 m²/g, 0.762 cm³/g and 4.92 nm, 389 m²/g, 0.837 cm³/g, in that order. The analytical performance of adsorbed urease on zeolite X (Na) surface was also investigated using cyclic voltammetry measurements, and the results showed distinct cathodic and anodic peaks by zeolite X (Na) 80 °C and zeolite X (Na) 100 °C. These zeolites' molar conductance was measured as a function of urea concentration and gave an average polynomial regression fit of 0.948. The findings in this study suggest that certain physicochemical properties, such as crystallization temperature and pH, are critical parameters for improving the morphological properties of zeolites synthesized from natural sources for various biomedical applications.

SEM-MLA-based Investigation of the Composition of Mafic Volcaniclastic Deposits from the Paraná Large Igneous Province, Brazil

NASA Astrophysics Data System (ADS)

Höfig, D. F.; Höfig, T. W.; Licht, O. A. B.; Haser, S.; Valore, L.

2017-12-01

Mafic volcaniclastic deposits (MVDs) have been widely reported in Large Igneous Provinces around the world, except for the Paraná Province (review by Ross et al., 2005: J Volcanol Geotherm Res, 145, pp. 281-314). Recent geochemical classification for this unit highlights, however, the occurrence of such deposits, connected to basic lava flows, mostly those High Ti - High P ones (Licht.: J Volcanol Geotherm Res, in press). In southern Brazil, MVDs intercalated with lava flows have been reported at 680 sites, showing conspicuous poorly sorted polymictic breccia at the base, grading to tuff breccias and red silicified tuffs at the top. Newly sampled rocks of Paraná mafic volcanoclastic deposits unravel important information about the composition utilizing Scanning Electron Microscopy-based Mineral Liberation Analysis. Overall, they show similar mineralogy presenting obsidian (25-40%), different phases of iron oxide (5-20%), quartz (10-25%), plagioclase (5-25%), celadonite (5-25%), and chlorite (5-10%). The breccias reveal a greater content of celadonite due to the presence of altered hypohyaline and hypocrystalline basaltic shards, whereas the tuffs are more enriched in glass. Different generations of plagioclase are attributed to various basalt shards and clasts as well vitroclasts found in the matrix. It is proposed that the MVDs were generated by explosive events due the interaction between the ascending mafic magma and deep aquifer systems and its siliciclastic matrix represents the country rock, i.e., the underneath Paleozoic sedimentary sequence of Paraná Basin.

Hydraulic characterization of overpressured tuffs in central Yucca Flat, Nevada Test Site, Nye County, Nevada

USGS Publications Warehouse

Halford, Keith J.; Laczniak, Randell J.; Galloway, Devin L.

2005-01-01

A sequence of buried, bedded, air-fall tuffs has been used extensively as a host medium for underground nuclear tests detonated in the central part of Yucca Flat at the Nevada Test Site. Water levels within these bedded tuffs have been elevated hundreds of meters in areas where underground nuclear tests were detonated below the water table. Changes in the ground-water levels within these tuffs and changes in the rate and distribution of land-surface subsidence above these tuffs indicate that pore-fluid pressures have been slowly depressurizing since the cessation of nuclear testing in 1992. Declines in ground-water levels concurrent with regional land subsidence are explained by poroelastic deformation accompanying ground-water flow as fluids pressurized by underground nuclear detonations drain from the host tuffs into the overlying water table and underlying regional carbonate aquifer. A hydraulic conductivity of about 3 x 10-6 m/d and a specific storage of 9 x 10-6 m-1 are estimated using ground-water flow models. Cross-sectional and three-dimensional ground-water flow models were calibrated to measured water levels and to land-subsidence rates measured using Interferometric Synthetic Aperture Radar. Model results are consistent and indicate that about 2 million m3 of ground water flowed from the tuffs to the carbonate rock as a result of pressurization caused by underground nuclear testing. The annual rate of inflow into the carbonate rock averaged about 0.008 m/yr between 1962 and 2005, and declined from 0.005 m/yr in 2005 to 0.0005 m/yr by 2300.

Highly crystallized nanometer-sized zeolite a with large Cs adsorption capability for the decontamination of water.

PubMed

Torad, Nagy L; Naito, Masanobu; Tatami, Junichi; Endo, Akira; Leo, Sin-Yen; Ishihara, Shinsuke; Wu, Kevin C-W; Wakihara, Toru; Yamauchi, Yusuke

2014-03-01

Nanometer-sized zeolite A with a large cesium (Cs) uptake capability is prepared through a simple post-milling recrystallization method. This method is suitable for producing nanometer-sized zeolite in large scale, as additional organic compounds are not needed to control zeolite nucleation and crystal growth. Herein, we perform a quartz crystal microbalance (QCM) study to evaluate the uptake ability of Cs ions by zeolite, to the best of our knowledge, for the first time. In comparison to micrometer-sized zeolite A, nanometer-sized zeolite A can rapidly accommodate a larger amount of Cs ions into the zeolite crystal structure, owing to its high external surface area. Nanometer-sized zeolite is a promising candidate for the removal of radioactive Cs ions from polluted water. Our QCM study on Cs adsorption uptake behavior provides the information of adsorption kinetics (e.g., adsorption amounts and rates). This technique is applicable to other zeolites, which will be highly valuable for further consideration of radioactive Cs removal in the future. Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Feldspar dissolution rates in the Topopah Spring Tuff, Yucca Mountain, Nevada

USGS Publications Warehouse

Bryan, C.R.; Helean, K.B.; Marshall, B.D.; Brady, P.V.

2009-01-01

Two different field-based methods are used here to calculate feldspar dissolution rates in the Topopah Spring Tuff, the host rock for the proposed nuclear waste repository at Yucca Mountain, Nevada. The center of the tuff is a high silica rhyolite, consisting largely of alkali feldspar (???60 wt%) and quartz polymorphs (???35 wt%) that formed by devitrification of rhyolitic glass as the tuff cooled. First, the abundance of secondary aluminosilicates is used to estimate the cumulative amount of feldspar dissolution over the history of the tuff, and an ambient dissolution rate is calculated by using the estimated thermal history. Second, the feldspar dissolution rate is calculated by using measured Sr isotope compositions for the pore water and rock. Pore waters display systematic changes in Sr isotopic composition with depth that are caused by feldspar dissolution. The range in dissolution rates determined from secondary mineral abundances varies from 10-16 to 10-17 mol s-1 kg tuff-1 with the largest uncertainty being the effect of the early thermal history of the tuff. Dissolution rates based on pore water Sr isotopic data were calculated by treating percolation flux parametrically, and vary from 10-15 to 10-16 mol s-1 kg tuff-1 for percolation fluxes of 15 mm a-1 and 1 mm a-1, respectively. Reconciling the rates from the two methods requires that percolation fluxes at the sampled locations be a few mm a-1 or less. The calculated feldspar dissolution rates are low relative to other measured field-based feldspar dissolution rates, possibly due to the age (12.8 Ma) of the unsaturated system at Yucca Mountain; because oxidizing and organic-poor conditions limit biological activity; and/or because elevated silica concentrations in the pore waters (???50 mg L-1) may inhibit feldspar dissolution. ?? 2009 Elsevier Ltd. All rights reserved.

Evaluation of the adsorptive behavior of cesium and strontium on hydroxyapatite and zeolite for decontamination of radioactive substances.

PubMed

Ozeki, K; Aoki, H

2016-08-12

Removal of radioactive substances, such as cesium (Cs) and strontium (Sr), has become an emerging issue after the Fukushima Daiichi Nuclear Power Plant Disaster. To assess the possibility that hydroxyapatite (HA) and zeolites can be used for removal of radioactive substances, the adsorption capacities of Cs and Sr on the HA and a zeolite were investigated. The influence of Fe ions on Cs and Sr adsorption on the HA and the zeolite was also evaluated, because Fe ions are the most effective inhibitor of Cs adsorption on the zeolite.In the Cs adsorption process on the HA and the zeolite, the zeolite showed a higher adsorption ratio than the HA, and the maximum sorption capacity of the zeolite was calculated as 196 mg/g, whereas the HA showed a higher Sr adsorption ratio than the zeolite. The maximum sorption capacity of Sr on the HA was 123 mg/g. Under coexistence with Fe, Cs adsorption on the zeolite decreased with increasing Fe concentration, reaching 2.0 ± 0.8% at 0.1 M Fe concentration. In contrast, Cs adsorption on the zeolite was improved by adding the HA. In the case of coexistence of the HA, the Cs adsorption on the mixture of the HA and the zeolite was 52.4% ± 3.6 % at 0.1 M Fe concentration, although Cs adsorption on the HA alone was quite low. In the Fe adsorption processes of the HA and the zeolite, the HA exhibited a maximum sorption capacity of 256 mg/g, which was much higher than that of the zeolite (111 mg/g). The high affinity of Fe on the HA contributes to the improvement of the deteriorated Cs adsorption on the zeolite due to Fe ions.

Sedimentary conditions of Upper Permian volcano-clastic rocks of Ayan-Yrahskiy anticlinorium (Verhoyansk-Kolyma orogen)

NASA Astrophysics Data System (ADS)

Astakhova, Anna; Khardikov, Aleksandr

2013-04-01

Sedimentation conditions of upper Permian volcano-clastic rocks of Ayan-Yurakhsky anticlinorium are the reason of discussions between researchers. It is important to correctly solve this problem. Investigation allows us to conclude that upper Permian sediments was formed due to high rate deltaic sedimentation on shelf and continental slope of epicontinental sea basin. More than 45 outcrops of upper Permian sediments were described within Ayan-Yurakhsky anticlinorium. Termochemical and X-ray phase, lithological facies, stadial, paleogeographic and others were applied. Investigation allows to classify following types: tuffs, tuffites of andesites, andesi-dacites, sandstone tuffs, siltstone tuffs and claystone tuffs. Two facies were deliniated in the research area: 1) delta channel facies 2) epicontinental sea shelf edge and continental slope. Delta channel facies are located on the south-west part of Aian-Yrahskiy anticlinorium. It is composed of silty packsand and psammitic tuff-siltstone alternation and gravel-psammitic andesi-dacitic tuffute and tuff-breccia bands. Sediments have cross-bedding, through cross-bedding, curvilinear lamination structures. Facies occurred during high rate deltaic sedimentation on the shelf of epicontinental sea. Epicontinental sea shelf edge and continental slope facies are located on the south-west part. Sediments are represented by large thickness tuff-siltstone with tuff-sandstone, tuff-madstone, tuff, tuffite bands and lenses. Large number of submarine landslides sediments provide evidence that there was high angle sea floore environment. 30-50 m diametr eruption centers were described by authors during geological traverses. They are located in Kulu river basin. Their locations are limited by deep-seated pre-ore fault which extended along Ayan-Yurakhsky anticlinorium. U-Pb SHRIMP method showed that the average age of circons, taken from eruption centers, is Permian (256,3±3,7 ma). This fact confirms our emphasis that eruption centers were the centre of underwater effusive explosions which had been occurred in late Permian time. Gold ore deposits mainly localized in the south of Ayan-Yurakhsky anticlinorium and associated with upper Permian deltaic facies sediments. Taking into account lithological facies feature and volcanoclastic origin of sediments it is reasonable to suggest expelled-catagenesis model of gold mineralization. Gold was entered in sedimentary basin with piroclastic material. During catagenesis stage gold migrated from complex of shelf edge and continental slope to fan delta front complex in conjunction with expelled water. The emplacement of ore gold deposits related with upper Permian sediments can be successfully predicted, using this model and associated techniques.

Characterization and antibacterial activity of silver exchanged regenerated NaY zeolite from surfactant-modified NaY zeolite.

PubMed

Salim, Mashitah Mad; Malek, Nik Ahmad Nizam Nik

2016-02-01

The antibacterial activity of regenerated NaY zeolite (thermal treatment from cetyltrimethyl ammonium bromide (CTAB)-modified NaY zeolite and pretreatment with Na ions) loaded with silver ions were examined using the broth dilution minimum inhibitory concentration (MIC) method against Escherichia coli (E. coli ATCC 11229) and Staphylococcus aureus (S. aureus ATCC 6538). X-ray diffraction (XRD), attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), energy dispersive X-ray (EDX) and chemical elemental analyses were used to characterize the regenerated NaY and AgY zeolites. The XRD patterns indicated that the calcination and addition of silver ions on regenerated NaY zeolite did not affect the structure of the regenerated NaY zeolite as the characteristic peaks of the NaY zeolite were retained, and no new peaks were observed. The regenerated AgY zeolite showed good antibacterial activity against both bacteria strains in distilled water, and the antibacterial activity of the samples increased with increasing Ag loaded on the regenerated AgY zeolite; the regenerated AgY zeolite was more effective against E. coli than S. aureus. However, the antibacterial activity of the regenerated AgY was not effective in saline solution for both bacteria. The study showed that CTAB-modified NaY zeolite materials could be regenerated to NaY zeolite using thermal treatment (550°C, 5h) and this material has excellent performance as an antibacterial agent after silver ions loading. Copyright © 2015 Elsevier B.V. All rights reserved.

A study on removing nitrogen from paddy field rainfall runoff by an ecological ditch-zeolite barrier system.

PubMed

Wang, Xiaoling; Li, Jiansheng; Li, Songmin; Zheng, Xiaotong

2017-12-01

Ecological ditches and zeolite have been widely applied in the removal of farmland nonpoint source pollution separately; little research has been done on the effects of combining the two methods. Specifically, few studies have focused on the in situ regeneration of zeolite. A 2-year field experiment using an ecological ditch-zeolite barrier system was conducted in a paddy field of summer rice-winter wheat rotation in the Taihu Lake area. The system consisted of two zeolite barriers positioned at one third and two thirds of the length of the ditch. This study focused on the effect of the system on in situ nitrogen removal during the rice-growing season. Simultaneous laboratory kinetics experiments with natural zeolite and a series of adsorbed zeolites taken from the ditch at different time were also conducted. The concentration removal efficiencies of total nitrogen are averaged 24.66% in 2014 and 30.39% in 2015. Meanwhile, the cumulative adsorption quantity of ammonia nitrogen by the two barriers accounted for 49.27% of the ammonia nitrogen removed in 2014 and 54.35% of that in 2015. The amount of nitrogen adsorbed by plants was larger than that adsorbed by zeolite. The breakthrough curves of the zeolite and the characteristics of the zeolite surface structures from different periods all demonstrated that the zeolite can be regenerated in situ in the case of unsaturated zeolite within the ecological ditch. It can be concluded that an ecological ditch-zeolite barrier system is a realistic option for removing nitrogen from agricultural rainfall runoff in the Taihu Lake area.

Zeolite Nanoparticles for Selective Sorption of Plasma Proteins

NASA Astrophysics Data System (ADS)

Rahimi, M.; Ng, E.-P.; Bakhtiari, K.; Vinciguerra, M.; Ahmad, H. Ali; Awala, H.; Mintova, S.; Daghighi, M.; Bakhshandeh Rostami, F.; de Vries, M.; Motazacker, M. M.; Peppelenbosch, M. P.; Mahmoudi, M.; Rezaee, F.

2015-11-01

The affinity of zeolite nanoparticles (diameter of 8-12 nm) possessing high surface area and high pore volume towards human plasma proteins has been investigated. The protein composition (corona) of zeolite nanoparticles has been shown to be more dependent on the plasma protein concentrations and the type of zeolites than zeolite nanoparticles concentration. The number of proteins present in the corona of zeolite nanoparticles at 100% plasma (in vivo state) is less than with 10% plasma exposure. This could be due to a competition between the proteins to occupy the corona of the zeolite nanoparticles. Moreover, a high selective adsorption for apolipoprotein C-III (APOC-III) and fibrinogen on the zeolite nanoparticles at high plasma concentration (100%) was observed. While the zeolite nanoparticles exposed to low plasma concentration (10%) exhibited a high selective adsorption for immunoglobulin gamma (i.e. IGHG1, IGHG2 and IGHG4) proteins. The zeolite nanoparticles can potentially be used for selectively capture of APOC-III in order to reduce the activation of lipoprotein lipase inhibition during hypertriglyceridemia treatment. The zeolite nanoparticles can be adapted to hemophilic patients (hemophilia A (F-VIII deficient) and hemophilia B (F-IX deficient)) with a risk of bleeding, and thus might be potentially used in combination with the existing therapy.

Zeolite Nanoparticles for Selective Sorption of Plasma Proteins.

PubMed

Rahimi, M; Ng, E-P; Bakhtiari, K; Vinciguerra, M; Ali Ahmad, H; Awala, H; Mintova, S; Daghighi, M; Bakhshandeh Rostami, F; de Vries, M; Motazacker, M M; Peppelenbosch, M P; Mahmoudi, M; Rezaee, F

2015-11-30

The affinity of zeolite nanoparticles (diameter of 8-12 nm) possessing high surface area and high pore volume towards human plasma proteins has been investigated. The protein composition (corona) of zeolite nanoparticles has been shown to be more dependent on the plasma protein concentrations and the type of zeolites than zeolite nanoparticles concentration. The number of proteins present in the corona of zeolite nanoparticles at 100% plasma (in vivo state) is less than with 10% plasma exposure. This could be due to a competition between the proteins to occupy the corona of the zeolite nanoparticles. Moreover, a high selective adsorption for apolipoprotein C-III (APOC-III) and fibrinogen on the zeolite nanoparticles at high plasma concentration (100%) was observed. While the zeolite nanoparticles exposed to low plasma concentration (10%) exhibited a high selective adsorption for immunoglobulin gamma (i.e. IGHG1, IGHG2 and IGHG4) proteins. The zeolite nanoparticles can potentially be used for selectively capture of APOC-III in order to reduce the activation of lipoprotein lipase inhibition during hypertriglyceridemia treatment. The zeolite nanoparticles can be adapted to hemophilic patients (hemophilia A (F-VIII deficient) and hemophilia B (F-IX deficient)) with a risk of bleeding, and thus might be potentially used in combination with the existing therapy.

Zeolite Nanoparticles for Selective Sorption of Plasma Proteins

PubMed Central

Rahimi, M.; Ng, E.-P.; Bakhtiari, K.; Vinciguerra, M.; Ahmad, H. Ali; Awala, H.; Mintova, S.; Daghighi, M.; Bakhshandeh Rostami, F.; de Vries, M.; Motazacker, M. M.; Peppelenbosch, M. P.; Mahmoudi, M.; Rezaee, F.

2015-01-01

The affinity of zeolite nanoparticles (diameter of 8–12 nm) possessing high surface area and high pore volume towards human plasma proteins has been investigated. The protein composition (corona) of zeolite nanoparticles has been shown to be more dependent on the plasma protein concentrations and the type of zeolites than zeolite nanoparticles concentration. The number of proteins present in the corona of zeolite nanoparticles at 100% plasma (in vivo state) is less than with 10% plasma exposure. This could be due to a competition between the proteins to occupy the corona of the zeolite nanoparticles. Moreover, a high selective adsorption for apolipoprotein C-III (APOC-III) and fibrinogen on the zeolite nanoparticles at high plasma concentration (100%) was observed. While the zeolite nanoparticles exposed to low plasma concentration (10%) exhibited a high selective adsorption for immunoglobulin gamma (i.e. IGHG1, IGHG2 and IGHG4) proteins. The zeolite nanoparticles can potentially be used for selectively capture of APOC-III in order to reduce the activation of lipoprotein lipase inhibition during hypertriglyceridemia treatment. The zeolite nanoparticles can be adapted to hemophilic patients (hemophilia A (F-VIII deficient) and hemophilia B (F-IX deficient)) with a risk of bleeding, and thus might be potentially used in combination with the existing therapy. PMID:26616161

Removal of calcium and magnesium ions from shale gas flowback water by chemically activated zeolite.

PubMed

Chang, Haiqing; Liu, Teng; He, Qiping; Li, Duo; Crittenden, John; Liu, Baicang

2017-07-01

Shale gas has become a new sweet spot of global oil and gas exploration, and the large amount of flowback water produced during shale gas extraction is attracting increased attention. Internal recycling of flowback water for future hydraulic fracturing is currently the most effective, and it is necessary to decrease the content of divalent cations for eliminating scaling and maintaining effectiveness of friction reducer. Zeolite has been widely used as a sorbent to remove cations from wastewater. This work was carried out to investigate the effects of zeolite type, zeolite form, activation chemical, activation condition, and sorption condition on removal of Ca 2+ and Mg 2+ from shale gas flowback water. Results showed that low removal of Ca 2+ and Mg 2+ was found for raw zeolite 4A and zeolite 13X, and the efficiency of the mixture of both zeolites was slightly higher. Compared with the raw zeolites, the zeolites after activation using NaOH and NaCl greatly improved the sorption performance, and there was no significant difference between dynamic activation and static activation. Dynamic sorption outperformed static sorption, the difference exceeding 40% and 7-70% for removal of Ca 2+ and Mg 2+ , respectively. Moreover, powdered zeolites outperformed granulated zeolites in divalent cation removal.

Energetics of sodium-calcium exchanged zeolite A.

PubMed

Sun, H; Wu, D; Guo, X; Shen, B; Navrotsky, A

2015-05-07

A series of calcium-exchanged zeolite A samples with different degrees of exchange were prepared. They were characterized by powder X-ray diffraction (XRD) and differential scanning calorimetry (DSC). High temperature oxide melt drop solution calorimetry measured the formation enthalpies of hydrated zeolites CaNa-A from constituent oxides. The water content is a linear function of the degree of exchange, ranging from 20.54% for Na-A to 23.77% for 97.9% CaNa-A. The enthalpies of formation (from oxides) at 25 °C are -74.50 ± 1.21 kJ mol(-1) TO2 for hydrated zeolite Na-A and -30.79 ± 1.64 kJ mol(-1) TO2 for hydrated zeolite 97.9% CaNa-A. Dehydration enthalpies obtained from differential scanning calorimetry are 32.0 kJ mol(-1) H2O for hydrated zeolite Na-A and 20.5 kJ mol(-1) H2O for hydrated zeolite 97.9% CaNa-A. Enthalpies of formation of Ca-exchanged zeolites A are less exothermic than for zeolite Na-A. A linear relationship between the formation enthalpy and the extent of calcium substitution was observed. The energetic effect of Ca-exchange on zeolite A is discussed with an emphasis on the complex interactions between the zeolite framework, cations, and water.

Exploitation of Unique Properties of Zeolites in the Development of Gas Sensors

PubMed Central

Zheng, Yangong; Li, Xiaogan; Dutta, Prabir K.

2012-01-01

The unique properties of microporous zeolites, including ion-exchange properties, adsorption, molecular sieving, catalysis, conductivity have been exploited in improving the performance of gas sensors. Zeolites have been employed as physical and chemical filters to improve the sensitivity and selectivity of gas sensors. In addition, direct interaction of gas molecules with the extraframework cations in the nanoconfined space of zeolites has been explored as a basis for developing new impedance-type gas/vapor sensors. In this review, we summarize how these properties of zeolites have been used to develop new sensing paradigms. There is a considerable breadth of transduction processes that have been used for zeolite incorporated sensors, including frequency measurements, optical and the entire gamut of electrochemical measurements. It is clear from the published literature that zeolites provide a route to enhance sensor performance, and it is expected that commercial manifestation of some of the approaches discussed here will take place. The future of zeolite-based sensors will continue to exploit its unique properties and use of other microporous frameworks, including metal organic frameworks. Zeolite composites with electronic materials, including metals will lead to new paradigms in sensing. Use of nano-sized zeolite crystals and zeolite membranes will enhance sensor properties and make possible new routes of miniaturized sensors. PMID:22666081

Antimicrobial Activity of Silver Ions Released from Zeolites Immobilized on Cellulose Nanofiber Mats.

PubMed

Rieger, Katrina A; Cho, Hong Je; Yeung, Hiu Fai; Fan, Wei; Schiffman, Jessica D

2016-02-10

In this study, we exploit the high silver ion exchange capability of Linde Type A (LTA) zeolites and present, for the first time, electrospun nanofiber mats decorated with in-house synthesized silver (Ag(+)) ion exchanged zeolites that function as molecular delivery vehicles. LTA-Large zeolites with a particle size of 6.0 μm were grown on the surface of the cellulose nanofiber mats, whereas LTA-Small zeolites (0.2 μm) and three-dimensionally ordered mesoporous-imprinted (LTA-Meso) zeolites (0.5 μm) were attached to the surface of the cellulose nanofiber mats postsynthesis. After the three zeolite/nanofiber mat assemblies were ion-exchanged with Ag(+) ions, their ion release profiles and ability to inactivate Escherichia coli (E. coli) K12 were evaluated as a function of time. LTA-Large zeolites immobilized on the nanofiber mats displayed more than an 11 times greater E. coli K12 inactivation than the Ag-LTA-Large zeolites that were not immobilized on the nanofiber mats. This study demonstrates that by decorating nanometer to micrometer scale Ag(+) ion-exchanged zeolites on the surface of high porosity, hydrophilic cellulose nanofiber mats, we can achieve a tunable release of Ag(+) ions that inactivate bacteria faster and are more practical to use in applications over powder zeolites.

Percolation flux and Transport velocity in the unsaturated zone, Yucca Mountain, Nevada

USGS Publications Warehouse

Yang, I.C.

2002-01-01

The percolation flux for borehole USW UZ-14 was calculated from 14C residence times of pore water and water content of cores measured in the laboratory. Transport velocity is calculated from the depth interval between two points divided by the difference in 14C residence times. Two methods were used to calculate the flux and velocity. The first method uses the 14C data and cumulative water content data directly in the incremental intervals in the Paintbrush nonwelded unit and the Topopah Spring welded unit. The second method uses the regression relation for 14C data and cumulative water content data for the entire Paintbrush nonwelded unit and the Topopah Spring Tuff/Topopah Spring welded unit. Using the first method, for the Paintbrush nonwelded unit in boreholeUSW UZ-14 percolation flux ranges from 2.3 to 41.0 mm/a. Transport velocity ranges from 1.2 to 40.6 cm/a. For the Topopah Spring welded unit percolation flux ranges from 0.9 to 5.8 mm/a in the 8 incremental intervals calculated. Transport velocity ranges from 1.4 to 7.3 cm/a in the 8 incremental intervals. Using the second method, average percolation flux in the Paintbrush nonwelded unit for 6 boreholes ranges from 0.9 to 4.0 mm/a at the 95% confidence level. Average transport velocity ranges from 0.6 to 2.6 cm/a. For the Topopah Spring welded unit and Topopah Spring Tuff, average percolation flux in 5 boreholes ranges from 1.3 to 3.2 mm/a. Average transport velocity ranges from 1.6 to 4.0 cm/a. Both the average percolation flux and average transport velocity in the PTn are smaller than in the TS/TSw. However, the average minimum and average maximum values for the percolation flux in the TS/TSw are within the PTn average range. Therefore, differences in the percolation flux in the two units are not significant. On the other hand, average, average minimum, and average maximum transport velocities in the TS/TSw unit are all larger than the PTn values, implying a larger transport velocity for the TS/TSw although there is a small overlap.

Radiogenic Ingrowth of 40CA from Decay of 40K Provides a Powerful Tracer for Understanding the Origins of Felsic Magmas

NASA Technical Reports Server (NTRS)

Mills, Ryan D.; Simon, Justin I.; Depaolo, Donald J.; Bachmann, Olivier

2013-01-01

Over time high K/Ca continental crust produces a unique Ca isotopic reservoir, with measurable 40Ca excesses compared to Earth's mantle (?Ca=0). Thus, values of ?Cai > 1 indicate a significant crustal contribution to a magma. Values of ?Cai (<1) indistinguishable from mantle Ca indicate that the Ca in those magmas is either directly from the mantle, or is from partial melting of newly formed crust. So, whereas 40Ca excesses clearly define crustal contributions, mantle-like 40Ca/44Ca ratios are not as definitive. Here we present Ca isotopic measurements of intermediate to felsic igneous rocks from the western United States, and two crustal xenoliths found within the Fish Canyon Tuff (FCT). The two crustal xenoliths found within the 28.2 Ma FCT of the southern Rocky Mountain volcanic field (SRMVF) yield ?Ca values of 4 and 7.5, respectively. The 40Ca excesses of these possible source rocks are due to long-term in situ 40K decay and suggest that they are Precambrian in age. However, the FCT (?Cai 0.3) is within uncertainty of the mantle 40Ca/44Ca. Together, these data indicate that little Precambrian crust was involved in the petrogenesis of the FCT. Nd isotopic analyses of the FCT imply that it was generated from 10- 75% of an enriched component, and the Ca isotopic data appear to restrict that component to newly formed lower crust, or enriched mantle. However, the Ca isotopic data do permit assimilation of some crust with low Ca/Nd; decreasing the 143Nd/144Nd without adding much excess 40Ca to the FCT. Several other large tuffs from the SRMVF and from Yellowstone have ?Cai indistinguishable from the mantle. However, a few large tuffs from the SRMVF show significant 40Ca excesses. These tuffs (Wall Mountain, Blue Mesa, and Grizzly Peak) are likely sourced from near, or within the Colorado Mineral Belt. New isotopic measurements of Mesozoic and Tertiary granites from across the northern Great Basin show a range of ?Cai from 0 to 3. In these samples ?Cai is generally correlated with ?Sri and is broadly negatively correlated with ?Ndi. However, for granites with similar ?Ndi at a given general location ?Cai can vary significantly (1 to 2 epsilon units). In rocks where low ?Ndi could also be due to melting from enriched reservoirs in the mantle lithosphere, the combination of high ?Cai with low ?Ndi clearly identifies crustal melts.

Synthesis of novel perfluoroalkylglucosides on zeolite and non-zeolite catalysts.

PubMed

Nowicki, Janusz; Mokrzycki, Łukasz; Sulikowski, Bogdan

2015-04-08

Perfluoroalkylglucosides comprise a very important class of fluorine-containing surfactants. These compounds can be synthesized by using the Fisher reaction, starting directly from glucose and the required perfluoroalcohols. We wish to report on the use of zeolite catalysts of different structure and composition for the synthesis of perfluoroalkylglucosides when using glucose and 1-octafluoropentanol as substrates. Zeolites of different pore architecture have been chosen (ZSM-5, ZSM-12, MCM-22 and Beta). Zeolites were characterized by XRD, nitrogen sorption, scanning electron microscopy (SEM) and solid-state 27Al MAS NMR spectroscopy. The activity of the zeolite catalysts in the glycosidation reaction was studied in a batch reactor at 100 °C below atmospheric pressure. The performance of zeolites was compared to other catalysts, an ion-exchange resin (Purolite) and a montmorillonite-type layered aluminosilicate. The catalytic performance of zeolite Beta was the highest among the zeolites studied and the results were comparable to those obtained over Purolite and montmorillonite type catalysts.

Zeolite and swine inoculum effect on poultry manure biomethanation

NASA Astrophysics Data System (ADS)

Kougias, P. G.; Fotidis, I. A.; Zaganas, I. D.; Kotsopoulos, T. A.; Martzopoulos, G. G.

2013-03-01

Poultry manure is an ammonia-rich substrate that inhibits methanogenesis, causing severe problems to the anaerobic digestion process. In this study, the effect of different natural zeolite concentrations on the mesophilic anaerobic digestion of poultry waste inoculated with well-digested swine manure was investigated. A significant increase in methane production was observed in treatments where zeolite was added, compared to the treatment without zeolite.Methane production in the treatment with 10 g dm-3 of natural zeolite was found to be 109.75% higher compared to the treatment without zeolite addition. The results appear to be influenced by the addition of zeolite, which reduces ammonia toxicity in anaerobic digestion and by the ammonia-tolerant swine inoculum.

Natural zeolites in diet or litter of broilers.

PubMed

Schneider, A F; Almeida, D S De; Yuri, F M; Zimmermann, O F; Gerber, M W; Gewehr, C E

2016-04-01

This study aims to analyse the influence of adding natural zeolites (clinoptilolite) to the diet or litter of broilers and their effects on growth performance, carcass yield and litter quality. Three consecutive flocks of broilers were raised on the same sawdust litter, from d 1 to d 42 of age, and distributed in three treatments (control with no added zeolites, addition of 5 g/kg zeolite to diet and addition of 100 g/kg zeolites to litter). The addition of zeolites to the diet or litter did not affect growth performance or carcass yield. The addition of zeolites to the diet did not influence moisture content of the litter, ammonia volatilisation was reduced only in the first flock and pH of litter was reduced in the second and third flock. However, the addition of zeolites to the litter reduced moisture content, litter pH and ammonia volatilisation in all flocks analysed. The addition of 5 g/kg zeolite to the diet in three consecutive flocks was not effective in maintaining litter quality, whereas the addition of 100 g/kg natural zeolites to sawdust litter reduced litter moisture and ammonia volatilisation in three consecutive flocks raised on the same litter.

Utilization of Natural Zeolite from Ponorogo and Purworejo for Naphthol Substance Adsorption

NASA Astrophysics Data System (ADS)

Imandiani, Sundus; Indira, Christine; Johan, Anthony; Budiyono

2018-02-01

Indonesia has many zeolite producing areas yet untapped. Researchers developed the utilization of natural zeolites useful for the adsorption of naphthol dyes commonly found in batik waste. In this study researchers used natural zeolites from Purworejo and Ponorogo that are activated using hydrochloric acid that is used for adsorption. The purpose of this research is to know the effect of natural zeolite activation from Ponorogo and Purworejo on the effectiveness of adsorption of naphthol dyes widely used in batik industry. Natural zeolite was activated using HCl concentration of 1.3N; 1.8N; 3.2N; and 3.9N for 60 minutes. The methods are preparation of natural zeolite from Purworejo and Ponorogo, dealumination using hydrochloric acid, adsorption process of naphthol dyes using activated zeolite, and test of adsorption result with uv-vis spectrophotometry. The test results showed that the higher HCl concentration will increase adsorption capacity. This can be known from the concentration of naphthol dye which decreased both using natural zeolite Ponorogo and Purworejo. While the effectiveness of adsorption shows natural zeolite Purworejo has a greater adsorption capacity than Ponorogo with optimum conditions of dealumination using concentration HCl 3,9N.

Hydrothermal synthesis of free-template zeolite T from kaolin

NASA Astrophysics Data System (ADS)

Arshad, Sazmal E.; Yusslee, Eddy F.; Rahman, Md. Lutfor; Sarkar, Shaheen M.; Patuwan, Siti Z.

2017-12-01

Free-template zeolite T crystals were synthesized via hydrothermal synthesis by utilizing the activated kaolin as silica and alumina source, with the molar composition of 1 SiO2: 0.04 Al2O3: 0.26 Na2O: 0.09 K2O: 14 H2O. Observation of the formation of free-template zeolite crystals were done at temperature 90°C, 100 °C and 110 °C respectively. It was therefore determined that during the 120 h of the synthesis at 90 °C, zeolite T nucleated and formed a first competitive phase with zeolite L. As temperature increases to 100 °C, zeolite T presented itself as a major phase in the system at time 168 h. Subsequently, development of Zeolite T with second competitive phase of zeolite W was observed at temperature 110 °C. In this study, XRD and SEM instruments were used to monitor the behavior of zeolite T crystals with respect of temperature and time. By using natural resource of kaolin clay as a starting material, this paper hence aims to provide new findings in synthesis of zeolite T using low energy consumption and low production cost.

Investigating the Influence of Temperature on the Kaolinite-Base Synthesis of Zeolite and Urease Immobilization for the Potential Fabrication of Electrochemical Urea Biosensors

PubMed Central

Anderson, David Ebo; Balapangu, Srinivasan; Fleischer, Heidimarie N. A.; Viade, Ruth A.; Awandare, Gordon A.; Tiburu, Elvis K.

2017-01-01

Temperature-dependent zeolite synthesis has revealed a unique surface morphology, surface area and pore size which influence the immobilization of urease on gold electrode supports for biosensor fabrication. XRD characterization has identified zeolite X (Na) at all crystallization temperatures tested. However, N2 adsorption and desorption results showed a pore size and pore volume of zeolite X (Na) 60 °C, zeolite X (Na) 70 °C and zeolite X (Na) 90 °C to range from 1.92 nm to 2.45 nm and 0.012 cm3/g to 0.061 cm3/g, respectively, with no significant differences. The specific surface area of zeolite X (Na) at 60, 70 and 90 °C was 64 m2/g, 67 m2/g and 113 m2/g, respectively. The pore size, specific surface area and pore volumes of zeolite X (Na) 80 °C and zeolite X (Na) 100 °C were dramatically increased to 4.21 nm, 295 m2/g, 0.762 cm3/g and 4.92 nm, 389 m2/g, 0.837 cm3/g, in that order. The analytical performance of adsorbed urease on zeolite X (Na) surface was also investigated using cyclic voltammetry measurements, and the results showed distinct cathodic and anodic peaks by zeolite X (Na) 80 °C and zeolite X (Na) 100 °C. These zeolites’ molar conductance was measured as a function of urea concentration and gave an average polynomial regression fit of 0.948. The findings in this study suggest that certain physicochemical properties, such as crystallization temperature and pH, are critical parameters for improving the morphological properties of zeolites synthesized from natural sources for various biomedical applications. PMID:28786961

Effective solidification/stabilisation of mercury-contaminated wastes using zeolites and chemically bonded phosphate ceramics.

PubMed

Zhang, Shaoqing; Zhang, Xinyan; Xiong, Ya; Wang, Guoping; Zheng, Na

2015-02-01

In this study, two kinds of zeolites materials (natural zeolite and thiol-functionalised zeolite) were added to the chemically bonded phosphate ceramic processes to treat mercury-contaminated wastes. Strong promotion effects of zeolites (natural zeolite and thiol-functionalised zeolite) on the stability of mercury in the wastes were obtained and these technologies showed promising advantages toward the traditional Portland cement process, i.e. using Portland cement as a solidification agent and natural or thiol-functionalised zeolite as a stabilisation agent. Not only is a high stabilisation efficiency (lowered the Toxicity Characteristic Leaching Procedure Hg by above 10%) obtained, but also a lower dosage of solidification (for thiol-functionalised zeolite as stabilisation agent, 0.5 g g(-1) and 0.7 g g(-1) for chemically bonded phosphate ceramic and Portland cement, respectively) and stabilisation agents (for natural zeolite as stabilisation agent, 0.35 g g(-1) and 0.4 g g(-1) for chemically bonded phosphate ceramic and Portland cement, respectively) were used compared with the Portland cement process. Treated by thiol-functionalised zeolite and chemically bonded phosphate ceramic under optimum parameters, the waste containing 1500 mg Hg kg(-1) passed the Toxicity Characteristic Leaching Procedure test. Moreover, stabilisation/solidification technology using natural zeolite and chemically bonded phosphate ceramic also passed the Toxicity Characteristic Leaching Procedure test (the mercury waste containing 625 mg Hg kg(-1)). Moreover, the presence of chloride and phosphate did not have a negative effect on the chemically bonded phosphate ceramic/thiol-functionalised zeolite treatment process; thus, showing potential for future application in treatment of 'difficult-to-manage' mercury-contaminated wastes or landfill disposal with high phosphate and chloride content. © The Author(s) 2015.

Ammonium removal from high-strength aqueous solutions by Australian zeolite.

PubMed

Wijesinghe, D Thushari N; Dassanayake, Kithsiri B; Sommer, Sven G; Jayasinghe, Guttila Y; J Scales, Peter; Chen, Deli

2016-07-02

Removal of ammonium nitrogen (NH4(+)-N) particularly from sources which are highly rich in nitrogen is important for addressing environmental pollution. Zeolites, aluminosilicate minerals, are commonly used as commercial adsorbents and ion-exchange medium in number of commercial applications due to its high adsorption capacity of ammonium (NH4(+)). However, detailed investigations on NH4(+) adsorption and ion exchange capacities of Australian natural zeolites are rare, particularly under higher NH4(+) concentrations in the medium. Therefore, this study was conducted to determine NH4(+) adsorption characteristics of Australian natural zeolites at high NH4(+) concentrations with and without other chemical compounds in an aqueous solution. Results showed that initial NH4(+) concentration, temperature, reaction time, and pH of the solution had significant effects on NH4(+) adsorption capacity of zeolite. Increased retention time and temperature generally had a positive impact on adsorption. Freundlich model fitted well with adsorption process of Australian natural zeolites; however, Langmuir model had best fitted for the adsorption process of sodium (Na(+)) treated zeolites. NaCl treatment increased the NH4(+) adsorption capacity of Australian zeolites by 25% at 1000 mg-N, NH4(+) solution. The maximum adsorption capacity of both natural Australian zeolites and Na(+) treated zeolites were estimated as 9.48 and 11.83 mg-N/g, respectively, which is lower than many zeolites from other sources. Compared to the NH4(+) only medium, presence of other competitive ions and acetic acid in the medium (resembling composition in digested swine manure slurries) reduced NH4(+) removal of natural and Na(+) treated zeolites by 44% and 57%, respectively. This suggests detailed investigations are required to determine practically achievable NH4(+) -N removal potential of zeolites for applications in complex mediums such as animal manure slurries.

Research on Molecular Sieve Technology.

ERIC Educational Resources Information Center

Shah, Dhananjai B.; Hayhurst, David T.

1985-01-01

The zeolite synthesis and modification research program at Cleveland State University (Ohio) is described, including program philosophy and objectives, and research facilities. Also considers zeolite synthesis, adsorption on zeolites, kinetics of adsorption, and zeolite catalysis research. (JN)

Photochemical charge separation in zeolites: Electron transfer dynamics, nanocrystals and zeolitic membranes. Final technical report

DOE Office of Scientific and Technical Information (OSTI.GOV)

Dutta, Prabir K.

2001-09-30

Aluminosilicate zeolites provide an excellent host for photochemical charge separation. Because of the constraints provided by the zeolite, the back electron transfer from the reduced acceptor to the oxidized sensitizer is slowed down. This provides the opportunity to separate the charge and use it in a subsequent reaction for water oxidation and reduction. Zeolite-based ruthenium oxide catalysts have been found to be efficient for the water splitting process. This project has demonstrated the usefulness of zeolite hosts for photolytic splitting of water.

Volcanic stratigraphy of large-volume silicic pyroclastic eruptions during Oligocene Afro-Arabian flood volcanism in Yemen

NASA Astrophysics Data System (ADS)

Peate, Ingrid Ukstins; Baker, Joel A.; Al-Kadasi, Mohamed; Al-Subbary, Abdulkarim; Knight, Kim B.; Riisager, Peter; Thirlwall, Matthew F.; Peate, David W.; Renne, Paul R.; Menzies, Martin A.

2005-12-01

A new stratigraphy for bimodal Oligocene flood volcanism that forms the volcanic plateau of northern Yemen is presented based on detailed field observations, petrography and geochemical correlations. The >1 km thick volcanic pile is divided into three phases of volcanism: a main basaltic stage (31 to 29.7 Ma), a main silicic stage (29.7 to 29.5 Ma), and a stage of upper bimodal volcanism (29.5 to 27.7 Ma). Eight large-volume silicic pyroclastic eruptive units are traceable throughout northern Yemen, and some units can be correlated with silicic eruptive units in the Ethiopian Traps and to tephra layers in the Indian Ocean. The silicic units comprise pyroclastic density current and fall deposits and a caldera-collapse breccia, and they display textures that unequivocally identify them as primary pyroclastic deposits: basal vitrophyres, eutaxitic fabrics, glass shards, vitroclastic ash matrices and accretionary lapilli. Individual pyroclastic eruptions have preserved on-land volumes of up to ˜850 km3. The largest units have associated co-ignimbrite plume ash fall deposits with dispersal areas >1×107 km2 and estimated maximum total volumes of up to 5,000 km3, which provide accurate and precisely dated marker horizons that can be used to link litho-, bio- and magnetostratigraphy studies. There is a marked change in eruption style of silicic units with time, from initial large-volume explosive pyroclastic eruptions producing ignimbrites and near-globally distributed tuffs, to smaller volume (<50 km3) mixed effusive-explosive eruptions emplacing silicic lavas intercalated with tuffs and ignimbrites. Although eruption volumes decrease by an order of magnitude from the first stage to the last, eruption intervals within each phase remain broadly similar. These changes may reflect the initiation of continental rifting and the transition from pre-break-up thick, stable crust supporting large-volume magma chambers, to syn-rift actively thinning crust hosting small-volume magma chambers.

Effects of zeolites on cultures of marine micro-algae: A brief review.

PubMed

Fachini, Adriano; Vasconcelos, Maria Teresa S D

2006-10-01

The cation-exchange capacity of zeolites is well known and has been increasingly explored in different fields with both economic and environmental successes. In aquatic medium with low salinity, zeolites have found multiple applications. However, a review of the literature on the applications of zeolites in salt waters found relatively few articles, including some recently published papers. The purpose of this review is to present the state-of-the-art on applications of using zeolites for amending the trace elemental contents of salt water as well as the implications of this property for promoting marine micro-algal growth. This paper deals with the following features: Sorption capacity of zeolites including 1. application of zeolites in saltwater, 2. the role of silicon and zeolites on cultures of micro-algae, and 3. the role of organically chelated trace metals. The following competing factors have been identified as effects of zeolites on algal growth in salt water: (i) ammonia decrease: growth inhibition reduced; (ii) macro-nutrients increase, mainly silicon: stimulation of silicon-dependent algae; (iii) trace metals increase (desorption from zeolites) or decrease (adsorption): inhibition or stimulation, depending on the nature of the element and its concentration; and, (iv) changes in the chelating organics exudation: inhibition or stimulation of growth, depending on the (a) nature of the complexed element; (b) bioavailability of the complex; and (c) concentration of the elements simultaneously present in inorganic forms. Zeolites have been capable of stimulating the growth of the silicon-demanding marine micro-algae, like diatoms, mainly because they can act as a silicon buffer in seawater. Zeolites can also influence the yield of non-silicon-demanding algae, because the changes they can cause (liberation and adsorption of trace elements) in the composition of the medium. Zeolites have been capable of stimulating the growth of the marine micro-algae. However, the extent of ion exchange between zeolite and seawater, which conditions the effects, will depend on several factors: (1) initial metal concentration in seawater; (2) levels of trace metals in the zeolites (contaminants); (3) characteristics of the zeolites in terms of both ion-exchange capacity and specific affinities for the different cations; (4) quantity of zeolite per litre of solution; (5) pH and (6) response of the organism in terms of liberation of organic ligands. Therefore, a previous investigation in each particular case is recommended, in order to select the zeolitic characteristics and concentrations that will maximize the algal yield. Stimulation of phytoplankton growth can be economically relevant since phytoplankton constitutes the basis of the marine food webs and is required in fish farming nurseries in the marine aquaculture industry. Zeolites are cheap, only small amounts (few milligrams per liter of culture) are required and the addition of some micro-nutrients may be omitted. Therefore, the inclusion of zeolites in algal cultures in aquaculture may have economic advantages.

ZEOLITES: EFFECTIVE WATER PURIFIERS

EPA Science Inventory

Zeolites are known for their adsorption, ion exchange and catalytic properties. Various natural zeolites are used as odor and moisture adsorbents and water softeners. Due to their acidic nature, synthetic zeolites are commonly employed as solid acid catalysts in petrochemical ind...

Study of zeolite influence on analytical characteristics of urea biosensor based on ion-selective field-effect transistors

PubMed Central

2014-01-01

A possibility of the creation of potentiometric biosensor by adsorption of enzyme urease on zeolite was investigated. Several variants of zeolites (nano beta, calcinated nano beta, silicalite, and nano L) were chosen for experiments. The surface of pH-sensitive field-effect transistors was modified with particles of zeolites, and then the enzyme was adsorbed. As a control, we used the method of enzyme immobilization in glutaraldehyde vapour (without zeolites). It was shown that all used zeolites can serve as adsorbents (with different effectiveness). The biosensors obtained by urease adsorption on zeolites were characterized by good analytical parameters (signal reproducibility, linear range, detection limit and the minimal drift factor of a baseline). In this work, it was shown that modification of the surface of pH-sensitive field-effect transistors with zeolites can improve some characteristics of biosensors. PMID:24636423

Methods of using structures including catalytic materials disposed within porous zeolite materials to synthesize hydrocarbons

DOEpatents

Rollins, Harry W [Idaho Falls, ID; Petkovic, Lucia M [Idaho Falls, ID; Ginosar, Daniel M [Idaho Falls, ID

2011-02-01

Catalytic structures include a catalytic material disposed within a zeolite material. The catalytic material may be capable of catalyzing a formation of methanol from carbon monoxide and/or carbon dioxide, and the zeolite material may be capable of catalyzing a formation of hydrocarbon molecules from methanol. The catalytic material may include copper and zinc oxide. The zeolite material may include a first plurality of pores substantially defined by a crystal structure of the zeolite material and a second plurality of pores dispersed throughout the zeolite material. Systems for synthesizing hydrocarbon molecules also include catalytic structures. Methods for synthesizing hydrocarbon molecules include contacting hydrogen and at least one of carbon monoxide and carbon dioxide with such catalytic structures. Catalytic structures are fabricated by forming a zeolite material at least partially around a template structure, removing the template structure, and introducing a catalytic material into the zeolite material.

Preparation and characterization of polysulfone/zeolite mixed matrix membranes for removal of low-concentration ammonia from aquaculture wastewater.

PubMed

Moradihamedani, Pourya; Abdullah, Abdul Halim

2018-01-01

Removal of low-concentration ammonia (1-10 ppm) from aquaculture wastewater was investigated via polysulfone (PSf)/zeolite mixed matrix membrane. PSf/zeolite mixed matrix membranes with different weight ratios (90/10, 80/20, 70/30 and 60/40 wt.%) were prepared and characterized. Results indicate that PSf/zeolite (80/20) was the most efficient membrane for removal of low-concentration ammonia. The ammonia elimination by PSf/zeolite (80/20) from aqueous solution for 10, 7, 5, 3 and 1 ppm of ammonia was 100%, 99%, 98.8%, 96% and 95% respectively. The recorded results revealed that pure water flux declined in higher loading of zeolite in the membrane matrix due to surface pore blockage caused by zeolite particles. On the other hand, ammonia elimination from water was decreased in higher contents of zeolite because of formation of cavities and macrovoids in the membrane substructure.

Systems including catalysts in porous zeolite materials within a reactor for use in synthesizing hydrocarbons

DOEpatents

Rolllins, Harry W [Idaho Falls, ID; Petkovic, Lucia M [Idaho Falls, ID; Ginosar, Daniel M [Idaho Falls, ID

2012-07-24

Catalytic structures include a catalytic material disposed within a zeolite material. The catalytic material may be capable of catalyzing a formation of methanol from carbon monoxide and/or carbon dioxide, and the zeolite material may be capable of catalyzing a formation of hydrocarbon molecules from methanol. The catalytic material may include copper and zinc oxide. The zeolite material may include a first plurality of pores substantially defined by a crystal structure of the zeolite material and a second plurality of pores dispersed throughout the zeolite material. Systems for synthesizing hydrocarbon molecules also include catalytic structures. Methods for synthesizing hydrocarbon molecules include contacting hydrogen and at least one of carbon monoxide and carbon dioxide with such catalytic structures. Catalytic structures are fabricated by forming a zeolite material at least partially around a template structure, removing the template structure, and introducing a catalytic material into the zeolite material.

Brittle deformation and slope failure at the North Menan Butte tuff cone, Eastern Snake River Plain, Idaho

USGS Publications Warehouse

Okubo, Chris H.

2014-01-01

The manifestation of brittle deformation within inactive slumps along the North Menan Butte, a basaltic tuff cone in the Eastern Snake River Plain, is investigated through field and laboratory studies. Microstructural observations indicate that brittle strain is localized along deformation bands, a class of structural discontinuity that is predominant within moderate to high-porosity, clastic sedimentary rocks. Various subtypes of deformation bands are recognized in the study area based on the sense of strain they accommodate. These include dilation bands (no shear displacement), dilational shear bands, compactional shear bands and simple shear bands (no volume change). Measurements of the host rock permeability between the deformation bands indicate that the amount of brittle strain distributed throughout this part of the rock is negligible, and thus deformation bands are the primary means by which brittle strain is manifest within this tuff. Structural discontinuities that are similar in appearance to deformation bands are observed in other basaltic tuffs. Therefore deformation bands may represent a common structural feature of basaltic tuffs that have been widely misclassified as fractures. Slumping and collapse along the flanks of active volcanoes strongly influence their eruptive behavior and structural evolution. Therefore characterizing the process of deformation band and fault growth within basaltic tuff is key to achieving a more complete understanding of the evolution of basaltic volcanoes and their associated hazards.

Rapid synthesis of beta zeolites

DOEpatents

Fan, Wei; Chang, Chun -Chih; Dornath, Paul; Wang, Zhuopeng

2015-08-18

The invention provides methods for rapidly synthesizing heteroatom containing zeolites including Sn-Beta, Si-Beta, Ti-Beta, Zr-Beta and Fe-Beta. The methods for synthesizing heteroatom zeolites include using well-crystalline zeolite crystals as seeds and using a fluoride-free, caustic medium in a seeded dry-gel conversion method. The Beta zeolite catalysts made by the methods of the invention catalyze both isomerization and dehydration reactions.

Effects of ultrasonic treatment on zeolite NaA synthesized from by-product silica.

PubMed

Vaičiukynienė, Danutė; Kantautas, Aras; Vaitkevičius, Vitoldas; Jakevičius, Leonas; Rudžionis, Žymantas; Paškevičius, Mantas

2015-11-01

The synthesis of zeolite NaA from silica by-product was carried out in the presence of 20 kHz ultrasound at room temperature. Zeolites obtained in this type of synthesis were compared to zeolites obtained by performing conventional static syntheses under similar conditions. The sonication effects on zeolite NaA synthesis were characterized by phase identification, crystallinity etc. The effects of different parameters such as crystallization time and initial materials preparation methods on the crystallinity and morphology of the synthesized zeolites were investigated. The final products were characterized by XRD and FT-IR. It was possible to obtain crystalline zeolite NaA from by-product silica in the presence of ultrasound. Copyright © 2015 Elsevier B.V. All rights reserved.

Antimicrobial mortar surfaces for the improvement of hygienic conditions.

PubMed

De Muynck, W; De Belie, N; Verstraete, W

2010-01-01

To evaluate the effectiveness of various antimicrobial mortar formulations in inhibiting the growth of a selection of pathogens of environmental and hygienic concern. Mortar prisms containing triclosan-incorporated fibres or different concentrations of silver copper zeolites were incubated with Escherichia coli, Listeria monocytogenes, Salmonella enterica or Staphylococcus aureus at 4 or 20 degrees C for 24 h. From plate counting, a substantial bactericidal effect (>4 log units) could only be observed for the mortar specimens containing more than 3% zeolites on cement weight base, the effect being more pronounced at 20 degrees C compared to 4 degrees C. No inhibitory effect could be observed for mortar specimens containing antimicrobial fibres. Adenosinetriphosphate (ATP) measurements allowed for a rapid indication of the occurrence of antimicrobial activity. In order to obtain a bactericidal effect on mortar surfaces, concentrations of silver copper zeolites of more then 3% are required. To our knowledge, this is the first study in which the effectiveness of various antimicrobial mortar mixtures towards the inhibition of pathogens has been evaluated in a quantitative way. Antimicrobial concrete mixtures can be used for the improvement of the hygienic conditions in a variety of environments.

Co-remediation of the lead-polluted garden soil by exogenous natural zeolite and humic acids.

PubMed

Shi, Wei-yu; Shao, Hong-bo; Li, Hua; Shao, Ming-an; Du, Sheng

2009-08-15

The current study reported the co-remediation effect on the lead-polluted garden soil by zeolite and humic acids (HA), which was from comparing with the remediation of single zeolite in term of the lead fraction of sequential extraction in the soil and the distribution of lead in different parts of rape. Mixed treatment (zeolite and HA) and single treatment (zeolite) were, respectively, applied to the artificially polluted garden soil to examine the difference of their remediation effects in pot experiment. Results indicated that the co-remediation led to significantly greater (p<0.01) reduction in the lead concentration in plants than by singly adding to zeolite. The co-application of zeolite and HA reduced the available fraction of lead compounds, but slightly increased (p<0.01) the water-soluble fraction of lead compounds in the garden soil, compared with the application of single zeolite, especially in the severe lead-polluted soil (> or =1000 mg kg(-1)). This method might be an efficient way to remediate the lead-polluted soils on a large scale, although zeolite is a kind of hazardous material.

Synthesis of Zeolites Using the ADOR (Assembly-Disassembly-Organization-Reassembly) Route

PubMed Central

Wheatley, Paul S.; Čejka, Jiří; Morris, Russell E.

2016-01-01

Zeolites are an important class of materials that have wide ranging applications such as heterogeneous catalysts and adsorbents which are dependent on their framework topology. For new applications or improvements to existing ones, new zeolites with novel pore systems are desirable. We demonstrate a method for the synthesis of novel zeolites using the ADOR route. ADOR is an acronym for Assembly, Disassembly, Organization and Reassembly. This synthetic route takes advantage of the assembly of a relatively poorly stable that which can be selectively disassembled into a layered material. The resulting layered intermediate can then be organized in different manners by careful chemical manipulation and then reassembled into zeolites with new topologies. By carefully controlling the organization step of the synthetic pathway, new zeolites with never before seen topologies are capable of being synthesized. The structures of these new zeolites are confirmed using powder X-ray diffraction and further characterized by nitrogen adsorption and scanning electron microscopy. This new synthetic pathway for zeolites demonstrates its capability to produce novel frameworks that have never been prepared by traditional zeolite synthesis techniques. PMID:27078165

Carbon dioxide capture utilizing zeolites synthesized with paper sludge and scrap-glass.

PubMed

Espejel-Ayala, F; Corella, R Chora; Pérez, A Morales; Pérez-Hernández, R; Ramírez-Zamora, R M

2014-12-01

The present work introduces the study of the CO2 capture process by zeolites synthesized from paper sludge and scrap glass. Zeolites ZSM-5, analcime and wairakite were produced by means of two types of Structure Directing Agents (SDA): tetrapropilamonium (TPA) and ethanol. On the one hand, zeolite ZSM-5 was synthesized using TPA; on the other hand, analcime and wairakite were produced with ethanol. The temperature programmed desorption (TPD) technique was performed for determining the CO2 sorption capacity of these zeolites at two sorption temperatures: 50 and 100 °C. CO2 sorption capacity of zeolite ZSM-5 synthesized at 50 °C was 0.683 mmol/g representing 38.2% of the value measured for a zeolite ZSM-5 commercial. Zeolite analcime showed a higher CO2 sorption capacity (1.698 mmol/g) at 50 °C and its regeneration temperature was relatively low. Zeolites synthesized in this study can be used in the purification of biogas and this will produce energy without increasing the atmospheric CO2 concentrations. © The Author(s) 2014.

Effect of zinc oxide amounts on the properties and antibacterial activities of zeolite/zinc oxide nanocomposite.

PubMed

Alswat, Abdullah A; Ahmad, Mansor Bin; Saleh, Tawfik A; Hussein, Mohd Zobir Bin; Ibrahim, Nor Azowa

2016-11-01

Nanocomposites of zinc oxide loaded on a zeolite (Zeolite/ZnO NCs) were prepared using co-precipitation method. The ratio effect of ZnO wt.% to the Zeolite on the antibacterial activities was investigated. Various techniques were used for the nanocomposite characterization, including UV-vis, FTIR, XRD, EDX, FESEM and TEM. XRD patterns showed that ZnO peak intensity increased while the intensities of Zeolite peaks decreased. TEM images indicated a good distribution of ZnO-NPs onto the Zeolite framework and the cubic structure of the zeolite was maintained. The average particle size of ZnO-nanoparticles loaded on the surface of the Zeolite was in the range of 1-10nm. Moreover, Zeolite/ZnO NCs showed noticeable antibacterial activities against the tested bacteria; Gram- positive and Gram- negative bacteria, under normal light. The efficiency of the antibacterial increased with increasing the wt.% from 3 to 8 of ZnO NPs, and it reached 87% against Escherichia coli E266. Copyright © 2016 Elsevier B.V. All rights reserved.

Synthesis of Zeolites Using the ADOR (Assembly-Disassembly-Organization-Reassembly) Route.

PubMed

Wheatley, Paul S; Čejka, Jiří; Morris, Russell E

2016-04-03

Zeolites are an important class of materials that have wide ranging applications such as heterogeneous catalysts and adsorbents which are dependent on their framework topology. For new applications or improvements to existing ones, new zeolites with novel pore systems are desirable. We demonstrate a method for the synthesis of novel zeolites using the ADOR route. ADOR is an acronym for Assembly, Disassembly, Organization and Reassembly. This synthetic route takes advantage of the assembly of a relatively poorly stable that which can be selectively disassembled into a layered material. The resulting layered intermediate can then be organized in different manners by careful chemical manipulation and then reassembled into zeolites with new topologies. By carefully controlling the organization step of the synthetic pathway, new zeolites with never before seen topologies are capable of being synthesized. The structures of these new zeolites are confirmed using powder X-ray diffraction and further characterized by nitrogen adsorption and scanning electron microscopy. This new synthetic pathway for zeolites demonstrates its capability to produce novel frameworks that have never been prepared by traditional zeolite synthesis techniques.

Nanodispersed Suspensions of Zeolite Catalysts for Converting Dimethyl Ether into Olefins

NASA Astrophysics Data System (ADS)

Kolesnichenko, N. V.; Yashina, O. V.; Ezhova, N. N.; Bondarenko, G. N.; Khadzhiev, S. N.

2018-01-01

Nanodispersed suspensions that are effective in DME conversion and stable in the reaction zone in a three-phase system (slurry reactor) are obtained from MFI zeolite commercial samples (TsVM, IK-17-1, and CBV) in liquid media via ultrasonic treatment (UST). It is found that the dispersion medium, in which ultrasound affects zeolite commercial sample, has a large influence on particle size in the suspension. UST in the aqueous medium produces zeolite nanoparticles smaller than 50 nm, while larger particles of MFI zeolite samples form in silicone or hydrocarbon oils. Spectral and adsorption data show that when zeolites undergo UST in an aqueous medium, the acid sites are redistributed on the zeolite surface and the specific surface area of the mesopores increases. Preliminary UST in aqueous media of zeolite commercial samples (TsVM, IK-17-1, and CBV) affects the catalytic properties of MFI zeolite nanodispersed suspensions. The selectivity of samples when paraffins and olefins form is largely due to superacid sites consisting of OH groups of hydroxonium ion H3O+.

Oxidation of cyclohexane catalyzed by metal-ion-exchanged zeolites.

PubMed

Sökmen, Ilkay; Sevin, Fatma

2003-08-01

The ion-exchange rates and capacities of the zeolite NaY for the Cu(II), Co(II), and Pb(II) metal ions were investigated. Ion-exchange equilibria were achieved in approximately 72 h for all the metal ions. The maximum ion exchange of metal ions into the zeolite was found to be 120 mg Pb(II), 110 mg Cu(II), and 100 mg Co(II) per gram of zeolite NaY. It is observed that the exchange capacity of a zeolite varies with the exchanged metal ion and the amount of metal ions exchanged into zeolite decreases in the sequence Pb(II) > Cu(II) > Co(II). Application of the metal-ion-exchanged zeolites in oxidation of cyclohexane in liquid phase with visible light was examined and it is observed that the order of reactivity of the zeolites for the conversion of cyclohexane to cyclohexanone and cyclohexanol is CuY > CoY > PbY. It is found that conversion increases by increase of the empty active sites of a zeolite and the formation of cyclohexanol is favored initially, but the cyclohexanol is subsequently converted to cyclohexanone.

Highly mesoporous single-crystalline zeolite beta synthesized using a nonsurfactant cationic polymer as a dual-function template.

PubMed

Zhu, Jie; Zhu, Yihan; Zhu, Liangkui; Rigutto, Marcello; van der Made, Alexander; Yang, Chengguang; Pan, Shuxiang; Wang, Liang; Zhu, Longfeng; Jin, Yinying; Sun, Qi; Wu, Qinming; Meng, Xiangju; Zhang, Daliang; Han, Yu; Li, Jixue; Chu, Yueying; Zheng, Anmin; Qiu, Shilun; Zheng, Xiaoming; Xiao, Feng-Shou

2014-02-12

Mesoporous zeolites are useful solid catalysts for conversion of bulky molecules because they offer fast mass transfer along with size and shape selectivity. We report here the successful synthesis of mesoporous aluminosilicate zeolite Beta from a commercial cationic polymer that acts as a dual-function template to generate zeolitic micropores and mesopores simultaneously. This is the first demonstration of a single nonsurfactant polymer acting as such a template. Using high-resolution electron microscopy and tomography, we discovered that the resulting material (Beta-MS) has abundant and highly interconnected mesopores. More importantly, we demonstrated using a three-dimensional electron diffraction technique that each Beta-MS particle is a single crystal, whereas most previously reported mesoporous zeolites are comprised of nanosized zeolitic grains with random orientations. The use of nonsurfactant templates is essential to gaining single-crystalline mesoporous zeolites. The single-crystalline nature endows Beta-MS with better hydrothermal stability compared with surfactant-derived mesoporous zeolite Beta. Beta-MS also exhibited remarkably higher catalytic activity than did conventional zeolite Beta in acid-catalyzed reactions involving large molecules.

Water supply for the Nuclear Rocket Development Station at the U.S. Atomic Energy Commission's Nevada Test Site

USGS Publications Warehouse

Young, Richard Arden

1972-01-01

The Nuclear Rocket Development Station, in Jackass Flats, occupies about 123 square miles in the southwestern part of the U.S. Atomic Energy Commission's Nevada Test Site. Jackass Flats, an intermontane valley bordered by highlands on all sides except for a drainage outlet in the southwestern corner, has an average annual rainfall of 4 inches. Jackass Flats is underlain by alluvium, colluvium, and volcanic rocks of Cenozoic age and, at greater depth, by sedimentary rocks of Paleozoic age. The alluvium and the colluvium lie above the saturated zone throughout nearly all of Jackass Flats. The Paleozoic sedimentary rocks contain limestone and dolomite units that are excellent water producers elsewhere ; however, these units are too deep in Jackass Flats to be economic sources of water. The only important water-producing unit known in the vicinity of the Nuclear Rocket Development Station is a welded-tuff aquifer, the Topopah Spring Member of the Paintbrush Tuff, which receives no significant recharge. This member contains about 500 feet of highly fractured rock underlying an area 11 miles long and 3 miles wide in western Jackass Flats. Permeability of the aquifer is derived mostly from joints and fractures; however, some permeability may be derived from gas bubbles in the upper part of the unit. Transmissivity, obtained from pumping tests, ranges from 68,000 to 488,000 gallons per day per foot. Volume of the saturated part of the aquifer is about 3.5 cubic miles, and the average specific yield probably ranges from 1 to 5 percent. The volume of ground water in storage is probably within the range of 37-187 billion gallons. This large amount of water should be sufficient to supply the needs of the Nuclear Rocket Development Station for many years. Water at the Nuclear Rocket Development Station is used for public supply, construction, test-cell coolant, exhaust cooling, and thermal shielding during nuclear reactor and engine testing, and washdown. Present (1967) average consumption of water is 520,000 gallons per day--all supplied by one well. This supply well and a standby well have a production capability of 1.6 million gallons per day--adequate for present needs. Water in the welded-tuff aquifer is of the sodium bicarbonate type. Dissolved-solids content of the water in Jackass Flats is in the general range 230 milligrams per liter in the western part to 890 milligrams per liter in the eastern part.

POTASSIUM PERMANGANATE AND CLINOPTILOLITE ZEOLITE FOR IN SITU TREATMENT OF GROUND WATER CONTAMINATED WITH LANDFILL LEACHATE: LABORATORY STUDY

EPA Science Inventory

There are tens of thousands of closed landfills in the United States, many of whicih are unlined and sited on alluvial deposits. Landfills are of concern because leachate contains a variety of pollutants that can contaminate ground and surface water. Data from chemical analysis...

UTILITY OF ZEOLITES IN HAZARDOUS METAL REMOVAL FROM WATER

EPA Science Inventory

Zeolites are well known for their ion exchange, adsorption and acid catalysis properties. Different inorganic pollutants have been removed from water at room temperature by using synthetic zeolites. Zeolite Faujasite Y has been used to remove inorganic pollutants including arseni...

Antimicrobial properties of zeolite-X and zeolite-A ion-exchanged with silver, copper, and zinc against a broad range of microorganisms.

PubMed

Demirci, Selami; Ustaoğlu, Zeynep; Yılmazer, Gonca Altın; Sahin, Fikrettin; Baç, Nurcan

2014-02-01

Zeolites are nanoporous alumina silicates composed of silicon, aluminum, and oxygen in a framework with cations, water within pores. Their cation contents can be exchanged with monovalent or divalent ions. In the present study, the antimicrobial (antibacterial, anticandidal, and antifungal) properties of zeolite type X and A, with different Al/Si ratio, ion exchanged with Ag(+), Zn(2+), and Cu(2+) ions were investigated individually. The study presents the synthesis and manufacture of four different zeolite types characterized by scanning electron microscopy and X-ray diffraction. The ion loading capacity of the zeolites was examined and compared with the antimicrobial characteristics against a broad range of microorganisms including bacteria, yeast, and mold. It was observed that Ag(+) ion-loaded zeolites exhibited more antibacterial activity with respect to other metal ion-embedded zeolite samples. The results clearly support that various synthetic zeolites can be ion exchanged with Ag(+), Zn(2+), and Cu(2+) ions to acquire antimicrobial properties or ion-releasing characteristics to provide prolonged or stronger activity. The current study suggested that zeolite formulations could be combined with various materials used in manufacturing medical devices, surfaces, textiles, or household items where antimicrobial properties are required.

Timing and development of the Heise volcanic field, Snake River Plain, Idaho, western USA

USGS Publications Warehouse

Morgan, L.A.; McIntosh, W.C.

2005-01-01

The Snake River Plain (SRP) developed over the last 16 Ma as a bimodal volcanic province in response to the southwest movement of the North American plate over a fixed melting anomaly. Volcanism along the SRP is dominated by eruptions of explosive high-silica rhyolites and represents some of the largest eruptions known. Basaltic eruptions represent the final stages of volcanism, forming a thin cap above voluminous rhyolitic deposits. Volcanism progressed, generally from west to east, along the plain episodically in successive volcanic fields comprised of nested caldera complexes with major caldera-forming eruptions within a particular field separated by ca. 0.5-1 Ma, similar to, and in continuation with, the present-day Yellowstone Plateau volcanic field. Passage of the North American plate over the melting anomaly at a particular point in time and space was accompanied by uplift, regional tectonism, massive explosive eruptions, and caldera subsidence, and followed by basaltic volcanism and general subsidence. The Heise volcan ic field in the eastern SRP, Idaho, represents an adjacent and slightly older field immediately to the southwest of the Yellowstone Plateau volcanic field. Five large-volume (>0.5 km3) rhyolitic ignimbrites constitute a time-stratigraphic framework of late Miocene to early Pliocene volcanism for the study region. Field relations and high-precision 40Ar/39Ar age determinations establish that four of these regional ignimbrites were erupted from the Heise volcanic field and form the framework of the Heise Group. These are the Blacktail Creek Tuff (6.62 ?? 0.03 Ma), Walcott Tuff (6.27 ?? 0.04 Ma), Conant Creek Tuff (5.51 ?? 0.13 Ma), and Kilgore Tuff (4.45 ?? 0.05 Ma; all errors reported at ?? 2??). The fifth widespread ignimbrite in the regions is the Arbon Valley Tuff Member of the Starlight Formation (10.21 ?? 0.03 Ma), which erupted from a caldera source outside of the Heise volcanic field. These results establish the Conant Creek Tuff as a distinct and widespread ignimbrite in the Heise volcanic field, eliminating former confusion resulting from previous discordant K/Ar and fission-track dates. New 40Ar/39Ar determinations, when combined wi th geochemical, lithologic geophysical, and field data, define the volcanic and tectonic history of the Heise volcanic field and surrounding areas. Volcanic units erupted from the Heise volcanic field also provide temporal control for tectonic events associated with late Cenozoic extension in the Snake Range and with uplift of the Teton Range, Wyoming. In the Snake Range, movement of large (???0.10 km3) slide blocks of Mississippian limestone exposed 50 km to the east of the Heise field occurred between 6.3 and 5.5 Ma and may have been catastrophically triggered by the caldera eruption of the 5.51 ?? 0.13-Ma Conant Creek Tuff. This slide block movement of ???300 vertical meters indicates that the Snake Range had significant relief by at least 5.5 Ma. In Jackson Hole, the distribution of outflow facies of the 4.45 ?? 0.05-Ma Kilgore caldera in the Heise volcanic field on the eastern SRP indicates that the northern Teton Range was not a significant topographic feature at this time. ?? 2005 Geological Society of America.

Dacitic ash-flow sheet near Superior and Globe, Arizona

USGS Publications Warehouse

Peterson, Donald W.

1961-01-01

Remnants of a dacitic ash-flow sheet near Globe, Miama, and Superia, Arizona cover about 100 square miles; before erosion the area covered by the sheet was at least 400 square miles and perhaps as much as 1,500 square miles. Its maximum thickness is about 2,000 feet, its average thickness is about 500 feet, and its original volume was at least 40 cubic miles. It was erupted on an eroded surface with considerable relief. The main part of the deposit was thought by early workers to be a lava flow. Even after the distinctive character of welded tuffs and related rocks was discovered, the nature and origin of this deposit remained dubious because textures did not correspond to those in other welded tuff bodies. Yet a lava flow as silicic as this dacite would be viscous instead of spreading out as an extensive sheet. The purpose of this investigation has been to study the deposit, resolve the inconsistencies, and deduce its origin and history. Five stratigraphic zones are distinguished according to differences in the groundmass. From bottom to top the zones are basal tuff, vitrophyre, brown zone, gray zone, and white zone. The three upper zones are distinguished by colors on fresh surfaces, for each weathers to a similar shade of light reddish brown. Nonwelded basal tuff grades upward into the vitrophyre, which is a highly welded tuff. The brown and gray zones consist of highly welded tuff with a lithoidal groundmass. Degree of welding decreases progressively upward through the gray and the white zones, and the upper white zone is nonwelded. Textures are clearly outlined in the lower part of the brown zone, but upward they become more diffuse because of increasing devitrification. In the white zone, original textures are essentially obliterated, and the groundmass consists of spherulites and microcrystalline intergrowths. The chief groundmass minerals are cristobalite and sanidine, with lesser quartz and plagioclase. Phenocrysts comprise about 40 percent of the rock, and their relative proportions are fairly uniform. Almost three-fourths of the phenocrysts are plagioclase, one-tenth quartz, one-tenth biotite, and the remainder sanidine, magnetite, and hornblende, with accessory sphene, zircon, and appetite. Pumice fragments are nearly equidimensional near the top of the sheet, and downward they become progressively more flattened until they finally disappear. The zones and the pumice fragment flattening ration (ratio of length to height) provide means for recognizing several faults within the sheet. Twelve new chemical analyses are nearly uniform in composition. If named according to chemical composition, the rock would be a quartz latite, but when named according to phenocrysts, it is a dacite. From the field occurrence and the interpretation of relict textures, it is concluded that the deposit is an ash-flow sheet containing large amounts of welded tuff, and that it was emplaced by a type of nuee ardente instead of a lava flow or air-fall shower. The nature of zoning and trend of flattening ratios indicate a series of eruptions in rapid enough succession for the sheet to form a single cooling unit. Except in the lower part of the sheet, original textures were obscured by devitrification and crystallization during cooling. Nearly uniform mineralogy and chemistry suggest a single magnetic source. A nearly circular area, about 3? miles in diameter, of altered dacite and earlier volcanic rocks, bounded by intricately faulted and brecciated older rocks, may be the site of a caldera that represents the source of the eruptions.

The effect of pressure on open-framework silicates: elastic behaviour and crystal-fluid interaction

NASA Astrophysics Data System (ADS)

Gatta, G. D.; Lotti, P.; Tabacchi, G.

2018-02-01

The elastic behaviour and the structural evolution of microporous materials compressed hydrostatically in a pressure-transmitting fluid are drastically affected by the potential crystal-fluid interaction, with a penetration of new molecules through the zeolitic cavities in response to applied pressure. In this manuscript, the principal mechanisms that govern the P-behaviour of zeolites with and without crystal-fluid interaction are described, on the basis of previous experimental findings and computational modelling studies. When no crystal-fluid interaction occurs, the effects of pressure are mainly accommodated by tilting of (quasi-rigid) tetrahedra around O atoms that behave as hinges. Tilting of tetrahedra is the dominant mechanism at low-mid P-regime, whereas distortion and compression of tetrahedra represent the mechanisms which usually dominate the mid-high P regime. One of the most common deformation mechanisms in zeolitic framework is the increase of channels ellipticity. The deformation mechanisms are dictated by the topological configuration of the tetrahedral framework; however, the compressibility of the cavities is controlled by the nature and bonding configuration of the ionic and molecular content, resulting in different unit-cell volume compressibility in isotypic structures. The experimental results pertaining to compression in "penetrating" fluids, and thus with crystal-fluid interaction, showed that not all the zeolites experience a P-induced intrusion of new monoatomic species or molecules from the P-transmitting fluids. For example, zeolites with well-stuffed channels at room conditions (e.g. natural zeolites) tend to hinder the penetration of new species through the zeolitic cavities. Several variables govern the sorption phenomena at high pressure, among those: the "free diameters" of the framework cavities, the chemical nature and the configuration of the extra-framework population, the partial pressure of the penetrating molecule in the fluid (if mixed with other non-penetrating molecules), the rate of P-increase, the surface/volume ratio of the crystallites under investigations and the temperature at which the experiment is conducted. An overview of the intrusion phenomena of monoatomic species (e.g. He, Ar, Kr), small (e.g. H2O, CO2) and complex molecules, along with the P-induced polymerization phenomena (e.g. C2H2, C2H4, C2H6O, C2H6O2, BNH6, electrolytic MgCl2·21H2O solution) is provided, with a discussion of potential technological and geological implications of these experimental findings.

Synthesis and characterization of zeolite from coal fly ash

NASA Astrophysics Data System (ADS)

Liu, Yong; Luo, Qiong; Wang, Guodong; Li, Xianlong; Na, Ping

2018-05-01

Fly ash (FA) from coal-based thermal power plant was used to synthesize zeolite in NaOH solution with hydrothermal method in this work. Firstly, the effects of calcination and acid treatment on the removal of impurities in fly ash were studied. Then based on the pretreated FA, the effects of alkali concentration, reaction temperature and Si/Al ratio on the synthesis of zeolite were studied in detail. The mineralogy, morphology, thermal behavior, infrared spectrum and specific surface for the synthetic sample were investigated. The results indicated that calcination at 750 °C for 1.5 h can basically remove unburned carbon from FA, and 4 M hydrochloric acid treatment of calcined FA at 90 °C for 2 h will reduce the quality of about 34.3%wt, which are mainly iron, calcium and sulfur elements. The concentration of NaOH, reaction temperature and Si/Al ratio have important effect on the synthesis of zeolite. In this study, 0.5 M NaOH cannot obtain any zeolite. High temperature is beneficial to zeolite synthesis from FA, but easily lead to a variety of zeolites. The synthetic sample contains three kinds of zeolites such as zeolite P, sodalite and zeolite X, when the reaction conditions are 2 M NaOH and 120 °C for 24 h. In this research, quartz always exists in the synthetic sample, but will reduce with the increase of temperature. The synthetic zeolite has the specific surface area of about 42 m2 g‑1 and better thermal stability.

UTILITY OF ZEOLITES IN REMOVAL OF INORGANIC AND ORGANIC WATER POLLUTANTS

EPA Science Inventory

Zeolites are well known for their ion exchange, adsorption and acid catalysis properties. Different inorganic and organic pollutants have been removed from water at room temperature using various zeolites. Synthetic zeolite Faujasite Y has been used to remove inorganic pollutants...

Dispersible Exfoliated Zeolite Nanosheets and Their Application as a Selective Membrane

DOE Office of Scientific and Technical Information (OSTI.GOV)

Varoon, Kumar; Zhang, Xueyi; Elyassi, Bahman

2011-10-06

Thin zeolite films are attractive for a wide range of applications, including molecular sieve membranes, catalytic membrane reactors, permeation barriers, and low-dielectric-constant materials. Synthesis of thin zeolite films using high-aspect-ratio zeolite nanosheets is desirable because of the packing and processing advantages of the nanosheets over isotropic zeolite nanoparticles. Attempts to obtain a dispersed suspension of zeolite nanosheets via exfoliation of their lamellar precursors have been hampered because of their structure deterioration and morphological damage (fragmentation, curling, and aggregation). We demonstrated the synthesis and structure determination of highly crystalline nanosheets of zeolite frameworks MWW and MFI. The purity and morphological integritymore » of these nanosheets allow them to pack well on porous supports, facilitating the fabrication of molecular sieve membranes.« less

Planar Zeolite Film-Based Potentiometric Gas Sensors Manufactured by a Combined Thick-Film and Electroplating Technique

PubMed Central

Marr, Isabella; Reiß, Sebastian; Hagen, Gunter; Moos, Ralf

2011-01-01

Zeolites are promising materials in the field of gas sensors. In this technology-oriented paper, a planar setup for potentiometric hydrocarbon and hydrogen gas sensors using zeolites as ionic sodium conductors is presented, in which the Pt-loaded Na-ZSM-5 zeolite is applied using a thick-film technique between two interdigitated gold electrodes and one of them is selectively covered for the first time by an electroplated chromium oxide film. The influence of the sensor temperature, the type of hydrocarbons, the zeolite film thickness, and the chromium oxide film thickness is investigated. The influence of the zeolite on the sensor response is briefly discussed in the light of studies dealing with zeolites as selectivity-enhancing cover layers. PMID:22164042

Silver-Ion-Exchanged Nanostructured Zeolite X as Antibacterial Agent with Superior Ion Release Kinetics and Efficacy against Methicillin-Resistant Staphylococcus aureus.

PubMed

Chen, Shaojiang; Popovich, John; Iannuzo, Natalie; Haydel, Shelley E; Seo, Dong-Kyun

2017-11-15

As antibiotic resistance continues to be a major public health problem, antimicrobial alternatives have become critically important. Nanostructured zeolites have been considered as an ideal host for improving popular antimicrobial silver-ion-exchanged zeolites, because with very short diffusion path lengths they offer advantages in ion diffusion and release over their conventional microsized zeolite counterparts. Herein, comprehensive studies are reported on materials characteristics, silver-ion release kinetics, and antibacterial properties of silver-ion-exchanged nanostructured zeolite X with comparisons to conventional microsized silver-ion-exchanged zeolite (∼2 μm) as a reference. The nanostructured zeolites are submicrometer-sized aggregates (100-700 nm) made up of primary zeolite particles with an average primary particle size of 24 nm. The silver-ion-exchanged nanostructured zeolite released twice the concentration of silver ions at a rate approximately three times faster than the reference. The material exhibited rapid antimicrobial activity against methicillin-resistant Staphylococcus aureus (MRSA) with minimum inhibitory concentration (MIC) values ranging from 4 to 16 μg/mL after 24 h exposure in various growth media and a minimum bactericidal concentration (MBC; >99.9% population reduction) of 1 μg/mL after 2 h in water. While high concentrations of silver-ion-exchanged nanostructured zeolite X were ineffective at reducing MRSA biofilm cell viability, efficacy increased at lower concentrations. In consideration of potential medical applications, cytotoxicity of the silver-ion-exchanged nanostructured zeolite X was also investigated. After 4 days of incubation, significant reduction in eukaryotic cell viability was observed only at concentrations 4-16-fold greater than the 24 h MIC, indicating low cytotoxicity of the material. Our results establish silver-ion-exchanged nanostructured zeolites as an effective antibacterial material against dangerous antibiotic-resistant bacteria.

Status Report on the 40Ar/39Ar and U/Pb Dating of Tuffs in the Dewey Lake Formation of West Texas Towards Constraining the Permo-Triassic Magnetostratigraphic Time Scale

NASA Astrophysics Data System (ADS)

Chang, S.; Renne, P. R.; Mundil, R.

2007-12-01

A detailed magnetic polarity time scale for the Permo-Triassic Boundary interval, critical for correlating events in marine and terrestrial paleoenvironments, is not yet well-established. Recently, late Permian magnetostratigraphic studies have been reported for non-marine sections in Europe and South Africa (Szurlies et al., 2003; Nawrocki, 2004; Ward et al., 2005). However, these sections are devoid of index fossil suitable for correlation with marine successions and also lack age constraints from radioisotopic dating methods. In other words, it is dubious to correlate these magnetostratigraphic data with the GSSP Permo-Triassic boundary and mass extinction. The Dewey Lake red beds formation of West Texas, believed to be the youngest Permian formation in North America, has yielded high-quality paleomagnetic data (Molina-Garza et al., 1989; Steiner, 2001) and contains several silicic tuffs potentially enabling high-resolution calibration of the magnetic polarity time scale in this critical age range. The tuffs have yet to be placed into a regional stratigraphic or magnetostratigraphic framework, and it is unclear exactly how many distinct eruptive units are represented by the 7 distinct samples collected to date from widely separated (>160 km) localities. 40Ar/39Ar (sanidine and biotite) and U/Pb (zircon) studies reveal that all 7 sampled tuffs were probably erupted within several hundred ka of the Permo-Triassic boundary as dated at the Meishan GSSP section (Renne et al., 1995; Mundil et al., 2004) but results thus far are inadequate to convincingly resolve age differences between the various samples. U/Pb dating of some samples is severely challenged by Pb-loss from the zircons despite application of the Mattinson (2005) annealing/chemical abrasion technique. 40Ar/39Ar data have been obtained from as many as four different irradiations in order to reduce neutron fluence related error. We observe the familiar ~1% bias between U/Pb and 40Ar/39Ar ages. Biotite microprobe data, zircon U/Th TIMS data, and the absence of sanidine from some samples serve to help correlate or distinguish some samples despite irresolvable age differences; existing data suggest that 4 distinct tuffs are present in the Dewey Lake Formation. Resolving their ages convincingly will require further work, but it is clear from our results combined with previous magnetostratigraphic data that magnetic polarity reversals were relatively frequent in the latest Permian. Thus the uniqueness of correlations elsewhere with the Permo-Triassic boundary based on magnetostratigraphy alone are not well-founded.

Innovative In-Situ Remediation of Contaminated Sediments for Simultaneous Control of Contamination and Erosion. Part 2

DTIC Science & Technology

2011-10-01

00516 20 Table 10. Partitioning coefficients used in transport modeling. Metal Clinoptilolite Zeolite (ml/g) Phillipsite Zeolite (ml/g) As...3 and 5. Laboratory protocols used for these tests were the same as those used for the previously described zeolite bioassays. The significance...amendments. Two cases were simulated using the 1-dimensional model for clinoptilolite zeolite (ZC) and phillipsite zeolite (ZP). The results of the

[What a physician should know about zeolites].

PubMed

Boranić, M

2000-01-01

Zeolites are natural and synthetic hydrated crystalline aluminosilicates endowed with absorptive and ion exchange properties. They have found numerous and multifarous applications--in industry as catalysts and absorbents, in water sanitation for the removal of ammonia and heavy metals, in agriculture as fertilizers, and in animal husbandry as the absorbents of excreted material and as food additives. Medical applications have included the use in filtration systems for anesthesia or dialysis and as the contrast materials in NMR imaging. Recently, zeolite powders for external use have found application as deodorants, antimycotic agents and wound dressings. Peroral use of encapsulated zeolite powders enriched with vitamins, oligoelements or other ingredients has been claimed to exert beneficial medical effects. Ingestion of zeolites may be considered analogous to the clay eating (geophagia), considered in traditional medicine as a remedy for various illnesses. Being amphoteric, zeolites are partly soluble in acid or alkaline media, but within the physiological pH range the solubility is generally low. Minimal amounts of free aluminium or silicium from the ingested zeolites are resorbed from the gut. The bulk of ingested zeolite probably remains undissolved in the gut. In view of the ion exchange properties, zeolites may be expected to change the ionic content, pH and buffering capacity of the gastrointestinal secretions and to affect the transport through the intestinal epithelium. In addition, zeolites could affect the bacterial flora and the resorption of bacterial products, vitamins and oligoelements. The contact of zeolite particles with gastrointestinal mucosa may elicit the secretion of cytokines with local and systemic actions. Reactive silicium ions might react with biomolecules of the intestinal epithelium, and if resorbed, do so in other cells. Mutagenic and carcinogenic effects of zeolite particles have been described, resembling such effects of asbestos fibers. Thus, local and systemic effects of zeolites may be complex and interrelated, and an objective assessment requires appropriate experimental models.

'water splitting' by titanium exchanged zeolite A. Technical report

DOE Office of Scientific and Technical Information (OSTI.GOV)

Kuznicki, S.M.; Eyring, E.M.

1978-09-01

Visually detectable and chromatographically and mass spectrally identified hydrogen gas evolves from titanium (III) exchanged zeolite A immersed in water and illuminated with visible light. Titanium(III) exchanged zeolite X and zeolite Y do not produce this reaction. A photochemically produced, oxygenated titanium free radical (detected by electron spin resonance) not previously described is the species in the zeolite that reduces protons to molecular hydrogen. The other product of this reduction step is a nonradical, oxygenated titanium species of probable empirical formula TiO4. Heating the spent oxygenated titanium containing zeolite A under vacuum at 375 C restores over fifty percent ofmore » the free radical. Unlike previously reported systems, heating does not restore the original aquotitanium(III) species in the zeolite. Thus a means other than heating must be found to achieve a closed photochemical cycle that harnesses visible solar energy in the production of molecular hydrogen. The titanium exchanged zeolite A does, however, lend itself to a thermolysis of water previously described by Kasai and Bishop. (Author)« less

A family of zeolites with controlled pore size prepared using a top-down method

NASA Astrophysics Data System (ADS)

Roth, Wieslaw J.; Nachtigall, Petr; Morris, Russell E.; Wheatley, Paul S.; Seymour, Valerie R.; Ashbrook, Sharon E.; Chlubná, Pavla; Grajciar, Lukáš; Položij, Miroslav; Zukal, Arnošt; Shvets, Oleksiy; Čejka, Jiří

2013-07-01

The properties of zeolites, and thus their suitability for different applications, are intimately connected with their structures. Synthesizing specific architectures is therefore important, but has remained challenging. Here we report a top-down strategy that involves the disassembly of a parent zeolite, UTL, and its reassembly into two zeolites with targeted topologies, IPC-2 and IPC-4. The three zeolites are closely related as they adopt the same layered structure, and they differ only in how the layers are connected. Choosing different linkers gives rise to different pore sizes, enabling the synthesis of materials with predetermined pore architectures. The structures of the resulting zeolites were characterized by interpreting the X-ray powder-diffraction patterns through models using computational methods; IPC-2 exhibits orthogonal 12- and ten-ring channels, and IPC-4 is a more complex zeolite that comprises orthogonal ten- and eight-ring channels. We describe how this method enables the preparation of functional materials and discuss its potential for targeting other new zeolites.

ZEOLITE: "THE MAGIC STONE"; MAIN NUTRITIONAL, ENVIRONMENTAL, EXPERIMENTAL AND CLINICAL FIELDS OF APPLICATION.

PubMed

Laurino, Carmen; Palmieri, Beniamino

2015-08-01

zeolites (clinoptilolites) are a family of alluminosilicates and cations clustered to form macro aggregates by small individual cavities. In the medical area they are involved in detoxification mechanisms capturing ions and molecules into their holes. Actually, we classify about 140 types of natural and 150 synthetic zeolites, for specific and selective use. Clinoptilolite is a natural zeolite and it is the most widespread compound in the medical market. this review analyzes the main fields of zeolite utilization. we searched Pubmed/Medline using the terms "zeolite" and "clinoptilolite". in zoothechnology and veterinary medicine zeolite improves the pets' fitness, removes radioactive elements, aflatoxines and poisons. Zeolite displays also antioxidant, whitening, hemostatic and anti-diarrhoic properties, projected in human care. However very scanty clinical studies have been run up to now in immunodeficiency, oncology after chemotherapy and radiotherapy as adjuvants. further clinical investigations are urgently required after this review article publication which updates the state of the art. Copyright AULA MEDICA EDICIONES 2014. Published by AULA MEDICA. All rights reserved.

IR and NMR studies of hierarchical material obtained by the treatment of zeolite Y by ammonia solution

NASA Astrophysics Data System (ADS)

Gackowski, Mariusz; Kuterasiński, Łukasz; Podobiński, Jerzy; Sulikowski, Bogdan; Datka, Jerzy

2018-03-01

Ammonia treatment of ultrastable zeolite Y has a great impact on its features. XRD showed a partial loss of crystallinity coupled with a loss of long-distance zeolite ordering. However, a typical short-range zeolite ordering, in the light of 29Si NMR studies, was largely preserved. 27Al MAS NMR spectra evidenced that most of Al was located in zeolitic tetrahedral positions, but some of them adopted a distorted configuration. Evolution of zeolites acidity was followed quantitatively by using IR. In particular, such studies revealed the presence of strongly acidic Sisbnd OHsbnd Al groups. IR studies suggest also heterogeneity of these OH groups. The heterogeneity of Sisbnd OHsbnd Al groups was a consequence of the less ordered structure of zeolites treated with ammonia solutions. It was also found that the treatment with ammonia solutions yields hierarchical material. The samples revealed promising catalytic properties in the liquid phase isomerization of α-pinene. Zeolites desilicated with ammonia may constitute an inexpensive route yielding viable hierarchical catalysts.

Theoretical studies of alkyl radicals in the NaY and HY zeolites.

PubMed

Ghandi, Khashayar; Zahariev, Federico E; Wang, Yan Alexander

2005-08-18

Interplay of quantum mechanical calculations and experimental data on hyperfine coupling constants of ethyl radical in zeolites at several temperatures was engaged to study the geometries and binding energies and to predict the temperature dependence of hyperfine splitting of a series of alkyl radicals in zeolites for the first time. The main focus is on the hyperfine interaction of alkyl radicals in the NaY and HY zeolites. The hyperfine splitting for neutral free radicals and free radical cations is predicted for different zeolite environments. This information can be used to establish the nature of the muoniated alkyl radicals in the NaY and HY zeolites via muSR experiments. The muon hyperfine coupling constants of the ethane radical cation in these zeolites are very large with relatively little dependence on temperature. It was found that the intramolecular dynamics of alkyl free radicals are only weakly affected by their strong binding to zeolites. In contrast, the substrate binding has a significant effect on their intermolecular dynamics.

Mineralogical and geochemical studies on the Central Seruyan Pb-Zn deposits in Central Kalimantan, Indonesia

NASA Astrophysics Data System (ADS)

Choi, Y.; Lee, I.; Choi, B.; KIM, Y.; Moon, I.

2017-12-01

The Central Seruyan Pb-Zn deposit is located in Seruyan, Central Kalimantan Province in Indonesia. This deposit has been developed since last year and is still being investigated. The Pb-Zn deposit consists of two formations, Pinoh and Kuayan formation. The former is a metamorphic unit hosting schist, phyllite and gneiss, and the latter is a pyroclastic and volcanic unit includes intermediate volcanic rocks such as dacite, tuff and breccia. Most host rocks of the deposit is composed of the silicified porphyritic dacite and silicified phyllite and covered by silicified tuff. The joints and fractures within the wall rock has E-W trends. The Seruyan Pb-Zn deposit is considered as hydrothermal breccia type.In this study, we observe ore minerals and host rocks to understand the genesis of the Pb-Zn deposit with geochemical data. Pyrite, chalcopyrite, sphalerite and galena are major ore minerals and covellite and bornite are also observed as minor sulfide minerals. These ore minerals, except pyrite, usually occur within quartz or calcite veins indicating the influence of hydrothermal fluid. In the host rocks, dacite, has the altered minerals like sericite, chlorite, epidote and some clay minerals of hydrothermal origin. All minerals occur as massive form. Only some pyrites have an euhedral form. Small amount of Au, Ag and Mo are detected in major ore minerals in the EPMA (electron probe X-ray microanalyzer) analyses.

Petrogenesis and U-Pb zircon chronology of felsic tuffs interbedded with turbidites (Eastern Pontides Orogenic Belt, NE Turkey): Implications for Mesozoic geodynamic evolution of the eastern Mediterranean region and accumulation rates of turbidite sequences

NASA Astrophysics Data System (ADS)

Eyuboglu, Yener

2015-01-01

The Meso-Cenozoic geodynamic evolution of the Eastern Pontides Orogenic Belt, which is one of the key areas of the Alpine-Himalayan system, is still controversial due to lack of systematic geological, geophysical, geochemical and chronological data. The prevailing interpretation is that this belt represents the southern margin of Eurasia during the Mesozoic and its geodynamic evolution is related to northward subduction of oceanic lithosphere. This paper reports the first detailed geological, geochemical and chronological data from felsic tuffs interbedded with late Cretaceous turbidites in the Southern Zone of the Eastern Pontides Orogenic Belt. Individual tuff layers are thin, mostly < 2 m in thickness, implying that these are dominantly air-fall tuffs. Petrographic data indicate that the felsic tuffs, which exhibit various degrees of alteration, can be classified as crystal-rich and crystal-poor tuffs. The crystal-poor tuffs consist mainly of 45-65% devitrified glass shards and 10-20% broken quartz crystals, whereas the crystal-rich tuffs consist of > 50% crystals. The zircon U-Pb data show three statistically distinct ages at 84, 81 and 77 Ma, with uncertainties of about 1 Ma, suggesting that tuff-forming late Cretaceous magmatism started about 84 Ma ago and was episodically active over a minimum of 7 Ma. The age data also indicate that the average accumulation rate of the turbiditic sequence that hosts the felsic tuffs remained constant between 36 and 40 cm/10 ky. Their enrichment in LIL and LRE elements relative to HFS and HRE elements, and also strongly negative Nb, Ta and Ti anomalies, are consistent with those of magmas generated by subduction-related processes. The tuffs have relatively low initial ratios of 143Nd/144Nd (0.512296-0.512484; εNd: - 2.1 and - 7.2) and 87Sr/86Sr (0.704896-0.706159). Their initial Pb isotopic compositions range from 18.604 to 18.646 for 206Pb/204Pb, from 15.644 to 15.654 for 207Pb/206Pb and from 38.712 to 38.763 for 208Pb/204Pb. The distribution of Sr-Nd isotopic compositions in the late Cretaceous igneous rocks from different locations of the Eastern Pontides Orogenic Belt is consistent with two-component mixing between depleted mantle and crust. However, the Pb isotopic data are not compatible with two-component mixing and require at least a third component. Considering all of the new data and also previous data such as southward migration and increasing potassium content of the late Cretaceous arc volcanism, the northward migration of Cenozoic igneous activity, northward drift of the belt since the late Cretaceous and the existence of south-dipping reverse fault systems in the whole region, the Meso-Cenozoic geodynamic evolution of the Eastern Pontides Orogenic Belt can be best explained by southward subduction of Tethys oceanic lithosphere, rather than northward subduction.

Nanocomposites of zeolite-titanium(IV) oxides: Preparation, characterization, adsorption, photocatalytic and bactericidal properties

NASA Astrophysics Data System (ADS)

Domoroshchina, Elena; Kravchenko, Galina; Kuz'micheva, Galina

2017-06-01

NT/zeolite nanocomposites (NT - nanosized titanium(IV) oxides: η-phase and Hombifine N with anatase; zeolite: Beta(25), ZSM-5 with different modules Si/Al, MOR, or Y) have been obtained by two methods: modified cold-impregnation method (method 1) and in situ method of introduction of zeolites into the reaction mixture during the synthesis of NT by hydrolysis of TiOSO4×xH2SO4×yH2O or TiOSO4×2H2O aqueous solutions (method 2), performed for the first time. According to the X-ray data, the following differences in the NT:zeolite systems under investigation have been revealed: the mixture of zeolites and NT in nanocrystalline (Hombifine N/zeolite) or amorphous states (η-phase/zeolite, except for η-phase/MOR, where NT peaks are absent) (method 1), and the mixture of Y-zeolite and amorphous NT or only Y-zeolite without NT (method 2), which indicates the different levels of interaction between NT and zeolites in the systems studied. The best characteristics of properties (photocatalytic, adsorption, and antibacterial) have been revealed in the nanocomposites synthesized by the method 2. The correlation between the photoreaction rate constant (the k value) under UV irradiation in the presence of nanocomposites (kmax for NT/ZSM-5(12)) and the type of precursor, its pH, synthesis duration, NT:zeolite ratio, organic dye composition (methyl orange or Rhodamine G) has been established. The highest degree of extraction of P(V) ions from model aqueous systems has been observed in the presence of nanocomposites with the largest total surface area of all particles (Rmax = 99.48% for NT/MOR). The correlation between the sorption degree of P(V) ions and the modulus of zeolite is possible. Antibacterial activity in the dark towards Escherichia coli has been found for Y and Beta(25) zeolites and nanocomposites on their basis (methods 1 and 2) with the maximum diameter of bacterial growth inhibition (18 mm) obtained for NT/Beta(25) (method 2) synthesized only from TiOSO4×xH2SO4×yH2O precursor.

Geological and 40Ar/39Ar age constraints on late-stage Deccan rhyolitic volcanism, inter-volcanic sedimentation, and the Panvel flexure from the Dongri area, Mumbai

NASA Astrophysics Data System (ADS)

Sheth, Hetu C.; Pande, Kanchan

2014-04-01

Post-K-Pg Boundary Deccan magmatism is well known from the Mumbai area in the Panvel flexure zone. Represented by the Salsette Subgroup, it shows characters atypical of much of the Deccan Traps, including rhyolite lavas and tuffs, mafic tuffs and breccias, spilitic pillow basalts, and "intertrappean" sedimentary or volcanosedimentary deposits, with mafic intrusions as well as trachyte intrusions containing basaltic enclaves. The intertrappean deposits have been interpreted as formed in shallow marine or lagoonal environments in small fault-bounded basins due to syn-volcanic subsidence. We report a previously unknown sedimentary deposit underlying the Dongri rhyolite flow from the upper part of the Salsette Subgroup, with a westerly tectonic dip due to the Panvel flexure. We have obtained concordant 40Ar/39Ar ages of 62.6 ± 0.6 Ma (2σ) and 62.9 ± 0.2 Ma (2σ) for samples taken from two separate outcrops of this rhyolite. The results are significant in showing that (i) Danian inter-volcanic sedimentary deposits formed throughout Mumbai, (ii) the rock units are consistent with the stratigraphy postulated earlier for Mumbai, (iii) shale fragments known in some Dongri tuffs were likely derived from the sedimentary deposit under the Dongri rhyolite, (iv) the total duration of extrusive and intrusive Deccan magmatism was at least 8-9 million years, and (v) Panvel flexure formed, or continued to form, after 63 Ma, possibly even 62 Ma, and could not have formed by 65-64 Ma as concluded in a recent study.

Growth of zeolite crystals in the microgravity environment of space

NASA Technical Reports Server (NTRS)

Sacco, A., Jr.; Sand, L. B.; Collette, D.; Dieselman, K.; Crowley, J.; Feitelberg, A.

1986-01-01

Zeolites are hydrated, crystalline aluminosilicates with alkali and alkaling earth metals substituted into cation vacancies. Typically zeolite crystals are 3 to 8 microns. Larger cyrstals are desirable. Large zeolite crystals were produced (100 to 200 microns); however, they have taken restrictively long times to grow. It was proposed if the rate of nucleation or in some other way the number of nuclei can be lowered, fewer, larger crystals will be formed. The microgravity environment of space may provide an ideal condition to achieve rapid growth of large zeolite crystals. The objective of the project is to establish if large zeolite crystals can be formed rapidly in space.

Structure modification of natural zeolite for waste removal application

NASA Astrophysics Data System (ADS)

Widayatno, W. B.

2018-03-01

Tremendous industrialization in the last century has led to the generation of huge amount of waste. One of the recent hot research topics is utilizing any advance materials and methods for waste removal. Natural zeolite as an inexpensive porous material with a high abundance holds a key for efficient waste removal owing to its high surface area. However, the microporous structure of natural zeolite hinders the adsorption of waste with a bigger molecular size. In addition, the recovery of natural zeolite after waste adsorption into its pores should also be considered for continuous utilization of this material. In this study, the porosity of natural zeolite from Tasikmalaya, Indonesia, was hydrothermally-modified in a Teflon-lined autoclave filled with certain pore directing agent such as distilled water, KOH, and NH4OH to obtain hierarchical pore structure. After proper drying process, the as-treated natural zeolite is impregnated with iron cation and heat-treated at specified temperature to get Fe-embedded zeolite structure. XRD observation is carried out to ensure the formation of magnetic phase within the zeolite pores. The analysis results show the formation of maghemite phase (γ-Fe2O3) within the zeolite pore structure.

Chemistry of alkali cation exchanged faujasite and mesoporous NaX using alkyl halides and phosphates

NASA Astrophysics Data System (ADS)

Lee, Min-Hong

The purpose of this work was to increase the reactivity of Faujasite X (NaX) zeolite toward the reactive decontamination of materials subject to nucleophilic attack by means of zeolite cation optimization and by means of the synthesis of mesoporous Faujasite X. Primary alkyl halides and trialkyl phosphates have been the test materials on which the cation-optimized and mesoporous zeolites have been tested. In the alkali cation optimization work, reactions of methyl iodide and 1-chloropropane with alkali metal cation exchanged Faujasite zeolite X were investigated at room temperature. The reactivity of the framework and the product formation were shown to depend on zeolite framework counter-cation. A quantitative study of zeolite product formation has been carried out, primarily using solid-state NMR spectroscopy. Large alkali cations showed preference toward substitution chemistry. In contrast, alkyl halide exposed LiX and NaX zeolites underwent both substitution and elimination. Subsequently introduced water molecules led to hydrolysis of framework species that was sensitive to framework counter-cation. The mesoporous NaX zeolites work undertakes to test whether an improvement in surface chemical reactivity can be achieved by introducing mesopores into the already reactive nucleophilic microporous NaX zeolite. Incorporation of the polydiallyl dimethyl ammonium chloride (PDADMAC) template and the formation of mesopores in Faujasite X zeolite (NaX) were successful and well-characterized. The mesopores are proposed to have occurred from incorporation of the cationic PDADMAC polymer into the zeolite by compensating zeolite framework charge. Subsequent sodium cation exchange of calcined mesoporous NaX was shown to restore the chemical reactivity characteristic of as-synthesized NaX. Trialkyl organophosphorous compounds underwent substitution reactions. The reactivity of both microporous and mesoporous Faujasite zeolite X and the product formation was shown to depend on the length of the alkyl chain. Although introduced mesopores alleviated the limited reagent diffusion to reactive sites due to the microporosity of the NaX zeolites, no marked improvement in the product yields was achieved with either the 1-chloroalkanes or the trialkyl phosphates test compounds, regardless of alkyl chain length. The disappointing results have been attributed to lack of substantial net increase in the numbers of zeolite nucleophilic sites accompanying mesopore introduction.

Magmatism, ash-flow tuffs, and calderas of the ignimbrite flareup in the western Nevada volcanic field, Great Basin, USA

USGS Publications Warehouse

Christopher D. Henry,; John, David A.

2013-01-01

The western Nevada volcanic field is the western third of a belt of calderas through Nevada and western Utah. Twenty-three calderas and their caldera-forming tuffs are reasonably well identified in the western Nevada volcanic field, and the presence of at least another 14 areally extensive, apparently voluminous ash-flow tuffs whose sources are unknown suggests a similar number of undiscovered calderas. Eruption and caldera collapse occurred between at least 34.4 and 23.3 Ma and clustered into five ∼0.5–2.7-Ma-long episodes separated by quiescent periods of ∼1.4 Ma. One eruption and caldera collapse occurred at 19.5 Ma. Intermediate to silicic lavas or shallow intrusions commonly preceded caldera-forming eruptions by 1–6 Ma in any specific area. Caldera-related as well as other magmatism migrated from northeast Nevada to the southwest through time, probably resulting from rollback of the formerly shallow-dipping Farallon slab. Calderas are restricted to the area northeast of what was to become the Walker Lane, although intermediate and effusive magmatism continued to migrate to the southwest across the future Walker Lane.Most ash-flow tuffs in the western Nevada volcanic field are rhyolites, with approximately equal numbers of sparsely porphyritic (≤15% phenocrysts) and abundantly porphyritic (∼20–50% phenocrysts) tuffs. Both sparsely and abundantly porphyritic rhyolites commonly show compositional or petrographic evidence of zoning to trachydacites or dacites. At least four tuffs have volumes greater than 1000 km3, with one possibly as much as ∼3000 km3. However, the volumes of most tuffs are difficult to estimate, because many tuffs primarily filled their source calderas and/or flowed and were deposited in paleovalleys, and thus are irregularly distributed.Channelization and westward flow of most tuffs in paleovalleys allowed them to travel great distances, many as much as ∼250 km (original distance) to what is now the western foothills of the Sierra Nevada, which was not a barrier to westward flow of ash flows at that time. At least three tuffs flowed eastward across a north-south paleodivide through central Nevada. That tuffs could flow significant distances apparently uphill raises questions about the absolute elevation of the region and the elevation, relief, and location of the paleodivide.Calderas are equant to slightly elongate, at least 12 km in diameter, and as much as 35 km in longest dimension. Exceptional exposure of two caldera complexes that resulted from extensional faulting and tilting show that calderas subsided as much as 5 km as large piston-like blocks; caldera walls were vertical to steeply inward dipping to depths ≥4–5 km, and topographic walls formed by slumping of wall rock into the caldera were only slightly outboard (≤1 km) of structural margins.Most calderas show abundant post-collapse magmatism expressed as resurgent intrusions, ring-fracture intrusions, or intracaldera lavas that are closely related temporally (∼0–0.5 Ma younger) to caldera formation. Granitoid intrusions, which were emplaced at paleodepths ranging from <1 to ∼7 km, are compositionally similar to both intracaldera ash-flow tuffs and post-caldera lavas. Therefore in the western Nevada volcanic field, erupted caldera-forming tuffs commonly were the upper parts of large magma chambers that retained considerable volumes of magma after tuff eruption.Several calderas in the western Nevada volcanic field hosted large hydrothermal systems and underwent extensive hydrothermal alteration. Different types of hydrothermal systems (neutral-pH alkali-chloride and acid or low-pH magmatic-hydrothermal) may reflect proximity to (depth of) large resurgent intrusions. With the exception of the giant Round Mountain epithermal gold deposit, few known caldera-related hydrothermal systems are strongly mineralized. Major middle Cenozoic precious and base metal mineral deposits in and along the margins of the western Nevada volcanic field are mostly related to intrusive rocks that preceded caldera-forming eruptions.

Preparation of 13X from Waste Quartz and Photocatalytic Reaction of Methyl Orange on TiO2/ZSM-5, 13X and Y-Zeolite.

PubMed

Wang, Jia-Jie; Jing, You-Hai; Ouyang, Tong; Chang, Chang-Tang

2015-08-01

TiO2 photocatalytic reactions not only remove a variety of organic pollutants via complete mineralization, but also destroy the bacterial cell wall and cell membrane, thus playing an important bactericidal role. However, the post-filtration procedures to separate nanometer-levels of TiO2 and the gradual inactivity of photocatalyst during continuous use are defects that limit its application. In this case, we propose loading TiO2 on zeolite for easy separation and 13X is considered as a promising one. In our study, 13X-zeolite was prepared by a hydrothermal method and the source of Si was extracted from waste quartz sand. For comparison, commercial zeolite with different microporous and mesoporous diameters (ZSM-5 and Y-zeolites) were also used as TiO2 supports. The pore size of the three kinds of zeolites are as follows: Y-zeolite > 13X > ZSM-5. Different TiO2 loading content over ZSM-5, 13X and Y-zeolite were prepared by the sol-gel method. XRD, FTIR, BET, UV-vis, TGA and SEM were used for investigation of material characteristics. In addition, the efficiencies of mineralization and photodegradation were studied in this paper. The effects of the loading ratio of TiO2 over zeolites, initial pH, and concentration on photocatalytic performance are investigated. The relationship between best loading content of TiO2 and pore size of the zeolite was studied. The possible roles of the ZSM-5, 13X-zeolites and Y-zeolites support on the reactions and the possible mechanisms of effects were also explored. The best loading content of TiO2 over ZSM-5, 13X and Y-zeolite was found to be 50 wt%, 12.5 wt% and 7 wt%, respectively. The optimum pH condition is 3 with TiO2 over ZSM-5, 13X-zeolites and Y-zeolites. The results showed that the degradation and mineralization efficiency of 12.5 wt%GT13X (TiO2 over 13X) after 90 min irradiation reached 57.9% and 22.0%, which was better than that of 7 wt%GTYZ (TiO2 over Y-zeolites) while much lower than that of 50 wt%GTZ (TiO2 over ZSM-5). The materials were recycled four times while the degradation was remained at a higher level.

Progress on Zeolite-membrane-aided Organic Acid Esterification

NASA Astrophysics Data System (ADS)

Makertiharta, I. G. B. N.; Dharmawijaya, P. T.

2017-07-01

Esterification is a common route to produce carboxylic acid esters as important intermediates in chemical and pharmaceutical industries. However, the reaction is equilibrium limited and needs to be driven forward by selective removal one of the products. There have been some efforts to selectively remove water from reaction mixture via several separation processes (such as pervaporation and reactive distillation). Integrated pervaporation and esterification has gained increasing attention towards. Inorganic zeolite is the most popular material for pervaporation due to its high chemical resistant and separation performance towards water. Zeolite also has proven to be an effective material in removing water from organic compound. Zeolite can act not only as selective layer but also simultaneously act as a catalyst on promoting the reaction. Hence, there are many configurations in integrating zeolite membrane for esterification reaction. As a selective layer to remove water from reaction mixture, high Si/Al zeolite is preferred to enhance its hydrophilicity. However, low Si/Al zeolite is unstable in acid condition due to dealumination thus eliminate its advantages. As a catalyst, acid zeolites (e.g. H-ZSM-5) provide protons for autoprotolysis of the carboxylic acid similar to other catalyst for esterification (e.g. inorganic acid, and ion exchange resins). There are many studies related to zeolite membrane aided esterification. This paper will give brief information related to zeolite membrane role in esterification and also research trend towards it.

Synthesis and characterization of Sn/zeolite and catalytic activity test in the esterification reaction of sludge oil

NASA Astrophysics Data System (ADS)

Alimuddin, Andi Hairil; Usman, Thamrin; Wahyuni, Nelly; Rudiyansyah, Prawatya, Yopa Eka; Astar, Ismail; Yustira, Yudi

2017-03-01

Synthesis of Sn-Zeolite has been made to use for esterification reaction of free fatty acids in sludge oil. Catalyst characterization was accomplished using X-Ray Diffraction (XRD), X-Ray Flourecence (XRF), and Fourier Transform Infra Red (FTIR). Catalyst Sn/zeolite was synthesized by impregnated Sn of SnCl2 into the zeolite. The amount of Sn impregnated base on the value of cation exchange capacity (CEC) of zeolites. Esterification reaction of fatty acids from sludge oil using Sn/Zeolite catalyst was did by variated the reaction time. XRD analysis results showed that the catalyst Sn/zeolite was dominated by modernit and quartz. XRF analysis results was increasing amount of Sn metal and the Si/Al ratio on Sn/zeolite catalyst along with addition of Sn metal. FTIR analysis results showed that the catalyst synthesized had Bronsted acid side (the spectrum 1639.4; 1656.7; 1654.8 cm-1) and the Lewis acid (spectrum 1400.2 and 1402.2 cm-1). The results showed that the optimum conditions of esterification reaction in 4 hours reaction time, 5% concentration of the catalyst, and molar ratio was about 1:10 with a conversion percentage of products reached 96.00%, which can be achieved with a ratio was about 4:1 between Sn and zeolite on Sn/zeolite catalyst.

Oxidative regeneration of toluene-saturated natural zeolite by gaseous ozone: the influence of zeolite chemical surface characteristics.

PubMed

Alejandro, Serguei; Valdés, Héctor; Manéro, Marie-Hélène; Zaror, Claudio A

2014-06-15

In this study, the effect of zeolite chemical surface characteristics on the oxidative regeneration of toluene saturated-zeolite samples is investigated. A Chilean natural zeolite (53% clinoptilolite, 40% mordenite and 7% quartz) was chemically modified by acid treatment with hydrochloric acid and by ion-exchange with ammonium sulphate. Thermal pre-treatments at 623 and 823K were applied and six zeolite samples with different chemical surface characteristics were generated. Chemical modification of natural zeolite followed by thermal out-gassing allows distinguishing the role of acidic surface sites on the regeneration of exhausted zeolites. An increase in Brønsted acid sites on zeolite surface is observed as a result of ammonium-exchange treatment followed by thermal treatment at 623K, thus increasing the adsorption capacity toward toluene. High ozone consumption could be associated to a high content of Lewis acid sites, since these could decompose ozone into atomic active oxygen species. Then, surface oxidation reactions could take part among adsorbed toluene at Brønsted acid sites and surface atomic oxygen species, reducing the amount of adsorbed toluene after the regenerative oxidation with ozone. Experimental results show that the presence of adsorbed oxidation by-products has a negative impact on the recovery of zeolite adsorption capacity. Copyright © 2014 Elsevier B.V. All rights reserved.

Fabrication of silver nanoparticles doped in the zeolite framework and antibacterial activity

PubMed Central

Shameli, Kamyar; Ahmad, Mansor Bin; Zargar, Mohsen; Yunus, Wan Md Zin Wan; Ibrahim, Nor Azowa

2011-01-01

Using the chemical reduction method, silver nanoparticles (Ag NPs) were effectively synthesized into the zeolite framework in the absence of any heat treatment. Zeolite, silver nitrate, and sodium borohydride were used as an inorganic solid support, a silver precursor, and a chemical reduction agent, respectively. Silver ions were introduced into the porous zeolite lattice by an ion-exchange path. After the reduction process, Ag NPs formed in the zeolite framework, with a mean diameter of about 2.12–3.11 nm. The most favorable experimental condition for the synthesis of Ag/zeolite nanocomposites (NCs) is described in terms of the initial concentration of AgNO3. The Ag/zeolite NCs were characterized by ultraviolet-visible spectroscopy, powder X-ray diffraction, transmission electron microscopy, scanning electron microscopy, energy dispersive X-ray fluorescence, and Fourier transform infrared. The results show that Ag NPs form a spherical shape with uniform homogeneity in the particle size. The antibacterial activity of Ag NPs in zeolites was investigated against Gram-negative bacteria (ie, Escherichia coli and Shigella dysentriae) and Gram-positive bacteria (ie, Staphylococcus aureus and methicillin-resistant Staphylococcus aureus) by disk diffusion method using Mueller–Hinton agar at different sizes of Ag NPs. All of the synthesized Ag/zeolite NCs were found to have antibacterial activity. These results show that Ag NPs in the zeolite framework can be useful in different biological research and biomedical applications. PMID:21383858

Adsorption and desorption of carbaryl on hexadecyl trimethyl ammonium bromide modified zeolite NaY using RGB portable photometer

NASA Astrophysics Data System (ADS)

Patdhanagul, Nopbhasinthu; Chanpaka, Saiphon; Intharaksa, Orapan; Sirival, Rujikarn; Thanomsith, Kannikar; Wongkwanklom, Sarayuth

2018-04-01

The carbaryl adsorption-desorption isotherms of zeolite NaY and hexadecyl trimethyl ammonium bromide (HTAB) modified zeolite NaY were investigated. Zeolite NaY was synthesized and modified by HTAB in the concentration range 0.1 - 10.0 mM. The adsorption isotherms indicated that zeolite modified with HTAB could significantly enhance the carbaryl adsorption capacity. Zeolite NaY modified with 5.0 mM HTAB gave great carbaryl adsorption because of hydrophilic surface. The 5.0 mM HTAB could adsorb up to 145.75 ppm g-1 of carbaryl which was equivalent to a 36.7% increase. The Surface area characterization showed the remaining of pore volume and pore size diameter and external surface area whereas the BET surface area and micropore surface area of modified zeolite slightly decreased. The XRD results indicate that modification of zeolite NaY with HTAB does not change the crystallinity of the starting zeolite. The elemental analysis indicated that the Si/Al ratio of synthesized zeolite NaY was close to 2.43. Desorption of carbaryl was tested by organic solvents such as methanol, ethanol, tetrahydrofuran, hexane and Deionized water. The results demonstrated that the percentage desorption of methanol is the highest. Carbaryl was quantitatively desorbed with percentage desorption of 82-100 %. It indicated sorption mechanism of carbaryl on the modified sorbent which was principally driven by hydrophobic forces.

Fabrication of silver nanoparticles doped in the zeolite framework and antibacterial activity.

PubMed

Shameli, Kamyar; Ahmad, Mansor Bin; Zargar, Mohsen; Yunus, Wan Md Zin Wan; Ibrahim, Nor Azowa

2011-01-01

Using the chemical reduction method, silver nanoparticles (Ag NPs) were effectively synthesized into the zeolite framework in the absence of any heat treatment. Zeolite, silver nitrate, and sodium borohydride were used as an inorganic solid support, a silver precursor, and a chemical reduction agent, respectively. Silver ions were introduced into the porous zeolite lattice by an ion-exchange path. After the reduction process, Ag NPs formed in the zeolite framework, with a mean diameter of about 2.12-3.11 nm. The most favorable experimental condition for the synthesis of Ag/zeolite nanocomposites (NCs) is described in terms of the initial concentration of AgNO(3). The Ag/zeolite NCs were characterized by ultraviolet-visible spectroscopy, powder X-ray diffraction, transmission electron microscopy, scanning electron microscopy, energy dispersive X-ray fluorescence, and Fourier transform infrared. The results show that Ag NPs form a spherical shape with uniform homogeneity in the particle size. The antibacterial activity of Ag NPs in zeolites was investigated against Gram-negative bacteria (ie, Escherichia coli and Shigella dysentriae) and Gram-positive bacteria (ie, Staphylococcus aureus and methicillin-resistant Staphylococcus aureus) by disk diffusion method using Mueller-Hinton agar at different sizes of Ag NPs. All of the synthesized Ag/zeolite NCs were found to have antibacterial activity. These results show that Ag NPs in the zeolite framework can be useful in different biological research and biomedical applications.

Lithium modified zeolite synthesis for conversion of biodiesel-derived glycerol to polyglycerol

DOE Office of Scientific and Technical Information (OSTI.GOV)

Ayoub, Muhammad, E-mail: muhammad.ayoub@petronas.com.my; Abdullah, Ahmad Zuhairi, E-mail: chzuhairi@usm.my; Inayat, Abrar, E-mail: abrar.inayat@petronas.com.my

Basic zeolite has received significant attention in the catalysis community. These zeolites modified with alkaline are the potential replacement for existing zeolite catalysts due to its unique features with added advantages. The present paper covers the preparation of lithium modified zeolite Y (Li-ZeY) and its activity for solvent free conversion of biodiesel-derived glycerol to polyglycerol via etherification process. The modified zeolite was well characterized by X-ray diffraction (XRD), Scanning Electron Microscope (SEM) and Nitrogen Adsorption. The SEM images showed that there was no change in morphology of modified zeolite structure after lithium modification. XRD patterns showed that the structure ofmore » zeolite was sustained after lithium modification. The surface properties of parent and modified zeolite was also observed N{sub 2} adsortion-desorption technique and found some changes in surface area and pore size. In addition, the basic strength of prepared materials was measured by Hammet indicators and found that basic strength of Li-ZeY was highly improved. This modified zeolite was found highly thermal stable and active heterogamous basic catalyst for conversion of solvent free glycerol to polyglycerol. This reaction was conducted at different temperatures and 260 °C was found most active temperature for this process for reaction time from 6 to 12 h over this basic catalyst in the absence of solvent.« less

Electrochemical water splitting using nano-zeolite Y supported tungsten oxide electrocatalysts

NASA Astrophysics Data System (ADS)

Anis, Shaheen Fatima; Hashaikeh, Raed

2018-02-01

Zeolites are often used as supports for metals and metal oxides because of their well-defined microporous structure and high surface area. In this study, nano-zeolite Y (50-150 nm range) and micro-zeolite Y (500-800 nm range) were loaded with WO3, by impregnating the zeolite support with ammonium metatungstate and thermally decomposing the salt thereafter. Two different loadings of WO3 were studied, 3 wt.% and 5 wt.% with respect to the overall catalyst. The prepared catalysts were characterized for their morphology, structure, and surface areas through scanning electron microscope (SEM), XRD, and BET. They were further compared for their electrocatalytic activity for hydrogen evolution reaction (HER) in 0.5 M H2SO4. On comparing the bare micro-zeolite particles with the nano-form, the nano-zeolite Y showed higher currents with comparable overpotentials and lower Tafel slope of 62.36 mV/dec. WO3 loading brought about a change in the electrocatalytic properties of the catalyst. The overpotentials and Tafel slopes were observed to decrease with zeolite-3 wt.% WO3. The smallest overpotential of 60 mV and Tafel slope of 31.9 mV/dec was registered for nano-zeolite with 3 wt.% WO3, while the micro-zeolite gave an overpotential of 370 mV and a Tafel slope of 98.1 mV/dec. It was concluded that even with the same metal oxide loading, nano-zeolite showed superior performance, which is attributed to its size and hence easier escape of hydrogen bubbles from the catalyst.

Optimization for zeolite regeneration and nitrogen removal performance of a hypochlorite-chloride regenerant.

PubMed

Zhang, Wei; Zhou, Zhen; An, Ying; Du, Silu; Ruan, Danian; Zhao, Chengyue; Ren, Ning; Tian, Xiaoce

2017-07-01

Simultaneous zeolites regeneration and nitrogen removal were investigated by using a mixed solution of NaClO and NaCl (NaClO-NaCl solution), and effects of the regenerant on ammonium removal performance and textural properties of zeolites were analyzed by long-term adsorption and regeneration operations. Mixed NaClO-NaCl solution removed more NH 4 + exchanged on zeolites and converted more of them to nitrogen than using NaClO or NaCl solution alone. Response surface methodological analysis indicated that molar ratio of hypochlorite and nitrogen (ClO - /N), NaCl concentration and pH value all had significant effects on zeolites regeneration and NH 4 + conversion to nitrogen, and the optimum condition was obtained at ClO - /N of 1.75, NaCl concentration of 20 g/L and pH of 10.0. Zeolites regenerated by mixed NaClO-NaCl solution showed higher ammonium adsorption rate and lower capacity than unused zeolites. Zeolites and the regeneration solution were both effective even after 20 cycles of use. Composition and morphological analysis revealed that the main mineral species and surface morphology of zeolites before and after NaClO-NaCl regeneration were unchanged. Textural analysis indicated that NaClO-NaCl regeneration leads to an increased surface area of zeolites, especially the microporosity. The results indicated that NaClO-NaCl regeneration is an attractive method to achieve sustainable removal of nitrogen from wastewater through zeolite. Copyright © 2017 Elsevier Ltd. All rights reserved.

Removal of excess nutrients by Australian zeolite during anaerobic digestion of swine manure.

PubMed

Wijesinghe, D Thushari N; Dassanayake, Kithsiri B; Scales, Peter; Sommer, Sven G; Chen, Deli

2018-03-21

The objective of this study was to investigate the feasibility of using natural and NaCl-treated Australian zeolites to simultaneously remove excess nutrients from anaerobically digested swine manure. Ion adsorption and desorption properties of Australian zeolite during the anaerobic digestion of swine manure were investigated. Two experiments were conducted: the first was an adsorption experiment with multi-component solutions that corresponded with the ionic composition of swine manure digestates. The second experiment determined the effects of zeolite dose rates during anaerobic digestion of swine manure on the removal of N, P and K from solution. Adsorption isotherms confirmed selectivity for K + over NH 4 + by Australian natural and sodium zeolites. Therefore, NH 4 + removal was considerably reduced when there was simultaneous K + uptake. Natural zeolite desorbed more Ca 2+ during K + and NH 4 + adsorption than sodium zeolite. The ion exchange reaction was independent of the presence of P. P removal was very dependent on the pH of the medium. Natural Australian zeolite was shown to be a potential sorbent for the removal of NH 4 + , K + and P during the anaerobic digestion of swine manure. However, the application of high concentrations of zeolite at higher pH values (> 7.5) might not be appropriate for anaerobic digestion, because zeolite desorbed more Ca 2+ ions into the solution at the higher doses of zeolite and then availability of P for microbial growth might be reduced as a result of PO 4 3- precipitation with Ca 2+ at the higher pH.

Reactivity of propene, n-butene, and isobutene in the hydrogen transfer steps of n-hexane cracking over zeolites of different structure

DOE Office of Scientific and Technical Information (OSTI.GOV)

Lukyanov, D.B.

The reaction of n-hexane cracking over HZSM-5, HY zeolite and mordenite (HM) was studied in accordance with the procedure of the [beta]-test recently proposed for quantitative characterization of zeolite hydrogen transfer activity. It is shown that this procedure allows one to obtain quantitative data on propene, n-butene, and isobutene reactivities in the hydrogen transfer steps of the reaction. The results demonstrate that in the absence of steric constraints (large pore HY and HM zeolites) isobutene is approximately 5 times more reactive in hydrogen transfer than n-butene. The latter, in turn, is about 1.3 times more reactive than propene. With mediummore » pore HZSM-5, steric inhibition of the hydrogen transfer between n-hexane and isobutene is observed. This results in a sharp decrease in the isobutene reactivity: over HZSM-5 zeolites isobutene is only 1.2 times more reactive in hydrogen transfer than n-butene. On the basis of these data it is concluded that the [beta]-test measures the [open quotes]real[close quotes] hydrogen transfer activity of zeolites, i.e., the activity that summarizes the effects of the acidic and structural properties of zeolites. An attempt is made to estimate the [open quotes]ideal[close quotes] zeolite hydrogen transfer activity, i.e., the activity determined by the zeolite acidic properties only. The estimations obtained show that this activity is approximately 1.8 and 1.6 times higher for HM zeolite in comparison with HZSM-5 and HY zeolites, respectively. 16 refs., 4 figs., 2 tabs.« less

Supported rhenium complexes: almost uniform rhenium tricarbonyls synthesized from CH3Re(CO)5 and HY zeolite.

PubMed

Lobo-Lapidus, Rodrigo J; Gates, Bruce C

2010-11-02

Supported rhenium complexes were prepared from CH(3)Re(CO)(5) and dealuminated HY zeolite or NaY zeolite, each with a Si/Al atomic ratio of 30. The samples were characterized with infrared (IR) and extended X-ray absorption fine structure (EXAFS) spectroscopies. EXAFS data characterizing the sample formed by the reaction of CH(3)Re(CO)(5) with dealuminated HY zeolite show that the rhenium complexes were bonded to the zeolite frame, incorporating, on average, three carbonyl ligands per Re atom (as shown by Re-C and multiple-scattering Re-O EXAFS contributions). The IR spectra, consistent with this result, show that the supported rhenium carbonyls were bonded near aluminum sites of the zeolite, as shown by the decrease in intensity of the IR bands characterizing the acidic silanol groups resulting from the reaction of the rhenium carbonyl with the zeolite. This supported metal complex was characterized by narrow peaks in the ν(CO) region of the IR spectrum, indicating highly uniform species. In contrast, the species formed from CH(3)Re(CO)(5) on NaY zeolite lost fewer carbonyl ligands than those formed on HY zeolite and were significantly less uniform, as indicated by the greater breadth of the ν(CO) bands in the IR spectra. The results show the importance of zeolite H(+) sites for the formation of uniform supported rhenium carbonyls from CH(3)Re(CO)(5); the formation of such uniform complexes did not occur on the NaY zeolite.

Properties of Zeolite A Obtained from Powdered Laundry Detergent: An Undergraduate Experiment.

ERIC Educational Resources Information Center

Smoot, Alison L.; Lindquist, David A.

1997-01-01

Presents experiments that introduce students to the myriad properties of zeolites using the sodium form of zeolite A (Na-A) from laundry detergent. Experiments include extracting Na-A from detergent, water softening properties, desiccant properties, ion-exchange properties, and Zeolite HA as a dehydration catalyst. (JRH)

In-situ petrophysical properties of hotspot volcanoes. Results from ODP Leg 197, Detroit Seamount and HSDP II borehole, Hawaii

NASA Astrophysics Data System (ADS)

Kock, I.; Pechnig, R.; Buysch, A.; Clauser, C.

2003-04-01

During ODP Leg 197 an extensive logging program was run on Site 1203, Detroit Seamount. This seamount is part of the Emperor seamount chain, a continuation of the Hawaiian volcanic chain. Standard ODP/LDEO logging tool strings were used to measure porosity, density, resistivity, p- and s-wave velocities and gamma ray activity. The FMS-tool yielded detailed high resolution resistivity images of the borehole wall. By interpretation and statistical analysis of the logging parameters a petrophysical classification of the drilled rock content could be derived. The pillow lava recovered in the cores exhibits low porosity, low resistivity and high density. This indicates no or very little vesicles in the non-fractured rock unit. Compared to the pillow basalts, subaerial basalts show increasing porosity, gamma ray and potassium content and decreasing density, resistivity and velocity. A basalt with no or little vesicles and a basalt with average or many vesicles can clearly be distinguished. The volcaniclastics show lower resistivity, lower sonic velocities, higher porosities and lower densities than the basalts. Three different rock types can be distinguished within the volcaniclastics: Tuffs, resedimented tephra and breccia. The tuff shows medium porosity and density, low gamma ray and potassium content. The log responses from the resedimented tephra suggest that the tephra is more easily altered than the tuff. The log responses from the breccia lie between the tuff and tephra log responses, but the breccia can clearly be identified in the FMS borehole images. A similar rock content was found in the Hawaiian Scientific Drilling Project borehole. Gamma ray activity, electrical resistivity and sonic velocity were measured down to 2700 mbsl.. Compared to the 72-76 Ma old Detroit seamount basalts, the HSDP subaerial and submarine lava flows show a significant lower gamma ray activity, while sonic velocity and electrical resistivity are comparable. Deviations between the gamma ray activity might be due to the different primary compositions of the melt or to long lasting low temperature alteration. Investigations on this topic are in progress.

Dry method for recycling iodine-loaded silver zeolite

DOEpatents

Thomas, Thomas R.; Staples, Bruce A.; Murphy, Llewellyn P.

1978-05-09

Fission product iodine is removed from a waste gas stream and stored by passing the gas stream through a bed of silver-exchanged zeolite until the zeolite is loaded with iodine, passing dry hydrogen gas through the bed to remove the iodine and regenerate the bed, and passing the hydrogen stream containing the hydrogen iodide thus formed through a lead-exchanged zeolite which adsorbs the radioactive iodine from the gas stream and permanently storing the lead-exchanged zeolite loaded with radioactive iodine.

Differentiation of colloidal and dissolved silica: Analytical separation using spectrophotometry and inductively coupled plasma atomic emission spectrometry

USGS Publications Warehouse

Lewis-Russ, A.; Ranville, J.; Kashuba, A.T.

1991-01-01

A method is described that differentiates between solutions containing silica-dominated colloids and solutions that are essentially free of colloids. Suspensions of tuff particles were treated to remove colloids by centrifugation, filtration or both. Agreement of silica concentrations determined by inductively coupled plasma atomic emission spectrometry and by a spectrophotometric method was taken as an indication of colloid-free solutions. For two tuffs, centrifugation was effective for removing colloids. For the third, highly altered tuff, filtration was more effective for removing colloids.

Modeling cation/anion-water interactions in functional aluminosilicate structures.

PubMed

Richards, A J; Barnes, P; Collins, D R; Christodoulos, F; Clark, S M

1995-02-01

A need for the computer simulation of hydration/dehydration processes in functional aluminosilicate structures has been noted. Full and realistic simulations of these systems can be somewhat ambitious and require the aid of interactive computer graphics to identify key structural/chemical units, both in the devising of suitable water-ion simulation potentials and in the analysis of hydrogen-bonding schemes in the subsequent simulation studies. In this article, the former is demonstrated by the assembling of a range of essential water-ion potentials. These span the range of formal charges from +4e to -2e, and are evaluated in the context of three types of structure: a porous zeolite, calcium silicate cement, and layered clay. As an example of the latter, the computer graphics output from Monte Carlo computer simulation studies of hydration/dehydration in calcium-zeolite A is presented.

Formation of reactive oxygen by N2O decomposition over binuclear cationic sites of Fe-ferrierite zeolite: Periodic DFT + U study

NASA Astrophysics Data System (ADS)

Avdeev, Vasilii I.; Bedilo, Alexander F.

2018-03-01

The electronic nature of sites over Fe-ferrierite zeolite stabilizing active α-oxygen is analyzed by the periodic DFT + U approach. It is shown that two antiferromagnetically coupled Fe2+ cations with bridging OH-bonds form a stable bi-nuclear site of the [Fe2+<2OH>Fe2+] doped FER complex. Frontier orbitals of this complex populated by two electrons with minority spins are localized in the bandgap. As a result, [Fe2+<2OH>Fe2+] unit acquires the properties of a binuclear Lewis acid dipolarophile for 1,3-dipole N2O. First reaction step of N2O decomposition follows the Huisgen‧s concept of the 1,3-dipolar cycloaddition concept followed by the formation of reactive oxygen species Fesbnd O.

Zeolite crystal growth in space

NASA Technical Reports Server (NTRS)

Sacco, Albert, Jr.; Thompson, Robert W.; Dixon, Anthony G.

1991-01-01

The growth of large, uniform zeolite crystals in high yield in space can have a major impact on the chemical process industry. Large zeolite crystals will be used to improve basic understanding of adsorption and catalytic mechanisms, and to make zeolite membranes. To grow large zeolites in microgravity, it is necessary to control the nucleation event and fluid motion, and to enhance nutrient transfer. Data is presented that suggests nucleation can be controlled using chemical compounds (e.g., Triethanolamine, for zeolite A), while not adversely effecting growth rate. A three-zone furnace has been designed to perform multiple syntheses concurrently. The operating range of the furnace is 295 K to 473 K. Teflon-lined autoclaves (10 ml liquid volume) have been designed to minimize contamination, reduce wall nucleation, and control mixing of pre-gel solutions on orbit. Zeolite synthesis experiments will be performed on USML-1 in 1992.

Atomic sites and stability of Cs+ captured within zeolitic nanocavities

PubMed Central

Yoshida, Kaname; Toyoura, Kazuaki; Matsunaga, Katsuyuki; Nakahira, Atsushi; Kurata, Hiroki; Ikuhara, Yumi H.; Sasaki, Yukichi

2013-01-01

Zeolites have potential application as ion-exchangers, catalysts and molecular sieves. Zeolites are once again drawing attention in Japan as stable adsorbents and solidification materials of fission products, such as 137Cs+ from damaged nuclear-power plants. Although there is a long history of scientific studies on the crystal structures and ion-exchange properties of zeolites for practical application, there are still open questions, at the atomic-level, on the physical and chemical origins of selective ion-exchange abilities of different cations and detailed atomic structures of exchanged cations inside the nanoscale cavities of zeolites. Here, the precise locations of Cs+ ions captured within A-type zeolite were analyzed using high-resolution electron microscopy. Together with theoretical calculations, the stable positions of absorbed Cs+ ions in the nanocavities are identified, and the bonding environment within the zeolitic framework is revealed to be a key factor that influences the locations of absorbed cations. PMID:23949184

Effect of SrO content on Zeolite Structure

NASA Astrophysics Data System (ADS)

Widiarti, N.; Sari, U. S.; Mahatmanti, F. W.; Harjito; Kurniawan, C.; Prasetyoko, D.; Suprapto

2018-04-01

The aims of current studies is to investigate the effect of strontium oxide content (SrO) on synthesized zeolite. Zeolite was synthesized from Tetraethyl orthosilicate (TEOS) as precursors of SiO2 and aluminum isopropoxide (AIP) precursors. The mixture was aged for 3 days and hydrothermally treated for 6 days. The SrO content was added by impregnation method. The products were then characterized using X-Ray Diffraction (XRD), Fourier Transform Infrared (FTIR), and Surface Area Analyzer (SAA). The diffractogram confirmed the formation of Faujasite-like zeolite. However, after the addition of SrO, the crystallinity of zeolite was deformed. The diffractograms shows the amorphous phase of zeolite were decrease as the SrO content is increase. The structural changes was also observed from FTIR spectra which shows the shifting and peak formation. The surface area analysis showed that the increasing loading of SrO/Zeolites reduced the catalyst surface area.

ZEOLITE PERFORMANCE AS AN ANION EXCHANGER FOR ARSENIC SEQUESTRATION IN WATER

EPA Science Inventory

Zeolites are well known for their use in ion exchange and acid catalysis reactions. The use of zeolites in anion or ligand exchange reactions is less studied. The NH4+ form of zeolite Y (NY6, Faujasite) has been tested in this work to evaluate its performance for arsenic removal...

Potential of Ni supported on KH zeolite catalysts for carbon dioxide reforming of methane

NASA Astrophysics Data System (ADS)

Kaengsilalai, Athiya; Luengnaruemitchai, Apanee; Jitkarnka, Sirirat; Wongkasemjit, Sujitra

The catalytic activity of Ni on a series of catalysts supported on the synthesized KH zeolite for the CO 2 reforming of methane has been investigated. The KH zeolite supports were previously synthesized via silatrane and alumatrane precursors using the sol-gel process and hydrothermal microwave treatment. Eight percent Ni was impregnated onto the synthesized KH zeolites, which have different morphologies: called dog-bone, flower, and disordered shapes. The prepared Ni/KH zeolites were tested for their catalytic activity at 700 °C, at atmospheric pressure, and at a CH 4/CO 2 ratio of 1. The results showed that Ni supported on dog-bone and flower-shaped KH zeolites provided better activity than that of disordered KH zeolite due to higher CH 4 and CO 2 conversions, a higher H 2 production, and a smaller amount of coke formation on the catalyst surface. Furthermore, the stability of the Ni/KH zeolite was greatly superior to that of Ni supported on alumina and clinoptiolite catalysts after 65 h on stream.

Zeolites on Mars: Prospects for Remote Sensing

NASA Technical Reports Server (NTRS)

Gaffney, E. S.; Singer, R. B.; Kunkle, T. D.

1985-01-01

The Martian surface composition measured by Viking can be represented by several combinations of minerals incorporating major fractions of zeolites known to occur in altered mafic rocks and polar soils on Earth. The abundant occurrence of zeolites on Mars is consistent with what is known about both the physical and chemical environment of that planet. The laboratory reflectance spectra (0.65 to 2.55 microns) of a number of relatively pure zeolite minerals and some naturally occurring zeolite-clay soils were measured. All of the spectra measured are dominated by strong absorption near 1.4 and 1.9 microns and a steep reflectance drop longward of about 2.2 microns, all of which are due to abundant H2O. Weaker water overtone bands are also apparent, and in most cases there is spectral evidence for minor Fe(3+). In these features the zeolite spectra are similar to spectra of smectite clays which have abundant interlayer water. The most diagnostic difference between clay and zeolite spectra is the total absence in the zeolites of the weak structural OH absorption.

Physicochemical regeneration of high silica zeolite Y used to clean-up water polluted with sulfonamide antibiotics.

PubMed

Braschi, I; Blasioli, S; Buscaroli, E; Montecchio, D; Martucci, A

2016-05-01

High silica zeolite Y has been positively evaluated to clean-up water polluted with sulfonamides, an antibiotic family which is known to be involved in the antibiotic resistance evolution. To define possible strategies for the exhausted zeolite regeneration, the efficacy of some chemico-physical treatments on the zeolite loaded with four different sulfonamides was evaluated. The evolution of photolysis, Fenton-like reaction, thermal treatments, and solvent extractions and the occurrence in the zeolite pores of organic residues eventually entrapped was elucidated by a combined thermogravimetric (TGA-DTA), diffractometric (XRPD), and spectroscopic (FT-IR) approach. The chemical processes were not able to remove the organic guest from zeolite pores and a limited transformation on embedded molecules was observed. On the contrary, both thermal treatment and solvent extraction succeeded in the regeneration of the zeolite loaded from deionized and natural fresh water. The recyclability of regenerated zeolite was evaluated over several adsorption/regeneration cycles, due to the treatment efficacy and its stability as well as the ability to regain the structural features of the unloaded material. Copyright © 2015. Published by Elsevier B.V.

[Preparation of HDTMA-modified Zeolite and Its Performance in Nitro-phenol Adsorption from Wastewaters].

PubMed

Guo, Jun-yuan; Wang, Bin

2016-05-15

In this study, natural zeolite was modified by HDTMA. Effects of the modified conditions, HDTMA-modified zeolite doses, solution pH values, and reaction time on nitro-phenol removal were investigated, and the adsorption kinetics and isotherms were discussed. Compared with natural zeolite, HDTMA-modified zeolite showed better performance in nitro-phenol removal. An adsorption capacity of 2.53 mg · g⁻¹ was achieved when the concentration of HDTMA solution (pH = 10) was 1.2% in preparation of modified zeolite. This adsorption capacity was higher than that obtained by natural zeolite (0.54 mg · g⁻¹). In adsorption tests, when HDTMA- modified zeolite dose was adjusted to 8 g · L⁻¹, the removal efficiency of nitro-phenol reached 93.9% after 90 min reaction, with wastewater pH of 6. Furthermore, the nitro-phenol adsorption process could be well fitted to the pseudo-first-order kinetics model (R² > 0.90), whereas the adsorption isotherm results indicated that Langmuir model provided the best fitting for the equilibrium data at different temperatures, with R² of higher than 0.90.

Benzene carboxylic acid derivatized graphene oxide nanosheets on natural zeolites as effective adsorbents for cationic dye removal.

PubMed

Yu, Yang; Murthy, Bandaru N; Shapter, Joseph G; Constantopoulos, Kristina T; Voelcker, Nicolas H; Ellis, Amanda V

2013-09-15

Graphene oxide (GO) nanosheets were grafted to acid-treated natural clinoptilolite-rich zeolite powders followed by a coupling reaction with a diazonium salt (4-carboxybenzenediazoniumtetrafluoroborate) to the GO surface. Raman spectroscopy, Fourier transform infrared (FTIR) spectroscopy, and thermogravimetric analysis (TGA) revealed successful grafting of GO nanosheets onto the zeolite surface. The application of the adsorbents for the adsorption of rhodamine B from aqueous solutions was then demonstrated. After reaching adsorption equilibrium the maximum adsorption capacities were shown to be 50.25, 55.56 and 67.56 mg g(-1) for pristine natural zeolite, GO grafted zeolite (GO-zeolite) and benzene carboxylic acid derivatized GO-zeolite powders, respectively. The adsorption behavior was fitted to a Langmuir isotherm and shown to follow a pseudo-second-order reaction model. Further, a relationship between surface functional groups, pH and adsorption efficiency was established. Results indicate that benzene carboxylic acid derivatized GO-zeolite powders are environmentally favorable adsorbents for the removal of cationic dyes from aqueous solutions. Copyright © 2013 Elsevier B.V. All rights reserved.

Zeolite Crystal Growth (ZCG) Flight on USML-2

NASA Technical Reports Server (NTRS)

Sacco, Albert, Jr.; Bac, Nurcan; Warzywoda, Juliusz; Guray, Ipek; Marceau, Michelle; Sacco, Teran L.; Whalen, Leah M.

1997-01-01

The extensive use of zeolites and their impact on the world's economy has resulted in many efforts to characterize their structure, and improve the knowledge base for nucleation and growth of these crystals. The zeolite crystal growth (ZCG) experiment on USML-2 aimed to enhance the understanding of nucleation and growth of zeolite crystals, while attempting to provide a means of controlling the defect concentration in microgravity. Zeolites A, X, Beta, and Silicalite were grown during the 16 day - USML-2 mission. The solutions where the nucleation event was controlled yielded larger and more uniform crystals of better morphology and purity than their terrestrial/control counterparts. The external surfaces of zeolite A, X, and Silicalite crystals grown in microgravity were smoother (lower surface roughness) than their terrestrial controls. Catalytic studies with zeolite Beta indicate that crystals grown in space exhibit a lower number of Lewis acid sites located in micropores. This suggests fewer structural defects for crystals grown in microgravity. Transmission electron micrographs (TEM) of zeolite Beta crystals also show that crystals grown in microgravity were free of line defects while terrestrial/controls had substantial defects.

Optimized Production of Coal Fly Ash Derived Synthetic Zeolites for Mercury Removal from Wastewater

NASA Astrophysics Data System (ADS)

Tauanov, Z.; Shah, D.; Itskos, G.; Inglezakis, V.

2017-09-01

Coal fly ash (CFA) derived synthetic zeolites have become popular with recent advances and its ever-expanding range of applications, particularly as an adsorbent for water and gas purification and as a binder or additive in the construction industry and agriculture. Among these applications, perpetual interest has been in utilization of CFA derived synthetic zeolites for removal of heavy metals from wastewater. We herein focus on utilization of locally available CFA for efficient adsorption of mercury from wastewater. To this end, experimental conditions were investigated so that to produce synthetic zeolites from Kazakhstani CFAs with conversion into zeolite up to 78%, which has remarkably high magnetite content. In particular, the effect of synthesis reaction temperature, reaction time, and loading of adsorbent were systematically investigated and optimized. All produced synthetic zeolites and the respective CFAs were characterized using XRD, XRF, PSA and porosimetric instruments to obtain microstructural and mineralogical data. Furthermore, the synthesized zeolites were studied for the removal of mercury from aqueous solutions. A comparison of removal eficiency and its relationship to the physical and chemical properties of the synthetic zeolites were analyzed and interpreted.

Comparative study of As (III) and Zn (II) removal from aqueous solutions using Philippine natural zeolite and alumina

NASA Astrophysics Data System (ADS)

Olegario-Sanchez, Eleanor; Pelicano, Christian Mark

2017-12-01

Herein, the heavy metal removal efficiency of Philippine natural zeolite is investigated through a comparative study with commercial alumina (Al2O3). XRD results revealed a high purity crystalline γ-Al2O3 and a natural zeolite having clinoptilolite (Na,K,Ca)2-3Al3(Al,Si)2Si13O36.12H2O and mordenite (Ca, Na2, K2)Al2Si10O24.7H2O as primary component minerals. Micro-pores and plate-like structures were observed on the surface of the natural zeolite. The natural zeolite has shown three times higher removal efficiency for Zn2+ ion than alumina. On the other hand, alumina exhibited comparable but smaller removal efficiency for As3+ as with that of natural zeolite. Alumina showed a higher capability of increasing the pH of both solutions compared with the natural zeolite. Based on removal efficiency and adsorbent costs, Philippine natural zeolite could be used as a low-cost alternative for wastewater treatment.

Are there Tuffs from Toba Supereruptions in Singapore?

NASA Astrophysics Data System (ADS)

Bergal-Kuvikas, O.; Bouvet de Maisonneuve, C.; Vazquez, J. A.

2016-12-01

Singapore is a dense transportation hub and the most highly populated area of SE Asia. In order to assess volcanic hazards for Singapore, we compiled a database of Quaternary eruptions from neighboring volcanoes and we investigated samples from 20 boreholes collected across 11 reservoirs and several natural outcrops in the NW parts of the city. We identified a deposit of white to slightly yellow clay with a visible thickness of 6-8 meters in the western part of Singapore. This deposit of very fine ash is silicic (SiO2 72-75 wt.%) and calk-alkaline (K2O 3.7-4.5 wt.%). The ash layer is clearly weathered as the LOI is around 5 wt.% and SEM images show the presence of clay minerals almost exclusively. Geochemical mapping shows that quartz crystals are characterized by textures similar to volcanic deposits. N-MORB normalized spiderdiagrams of whole-rocks show minimums in Nb and Ti, enrichments in LREE, and depletions of HREE. This suggests a subduction origin. One possible source for this voluminous weathered ash layer is the Toba caldera, which produced several super eruptions in the Quaternary (the Young Toba Tuff at 0.074 Ma, Middle Toba Tuff at 0.5 Ma, Old Toba Tuff at 0.84 Ma, and Haranggoal Dacite Tuff at 1.2 Ma). Recognizing distal Toba tuffs is problematic because most deposits are underwater. Most of the analyzed samples have geochemical compositions that are statistically similar to the Toba tuffs and characterized by high contents of HREE elements (e.g. Y, Er, Yb) and some REE (e.g. Eu, Ba, La, Th). Preliminary dating shows the presence of Triassic zircons, possibly due to geologic contamination. Additional dating is needed to ascertain the source and age of this ash. Our new geochemical data of likely distal Toba deposits will be an important component for tephrochronological and paleoenvironmental studies in addition to being of importance for hazards assessments in Singapore.

Carbonatite tuffs in the Laetolil Beds of Tanzania and the Kaiserstuhl in Germany

USGS Publications Warehouse

Hay, R.L.; O'Neil, J.R.

1983-01-01

Carbonatite lava and tephra are now well known. The only modern eruptive carbonatites, from Oldoinyo Lengai, Tanzania, are of alkali carbonatite, whereas all of the pre-modern examples are of calcite or dolomite. Chemical and stable isotope analyses were made of separate phases of Pliocene carbonatite tuffs of the Laetolil Beds in Tanzania and of Miocene carbonatite tuffs of the Kaiserstuhl in Germany in order to understand the reasons for this major difference. The Laetolil Beds contain numerous carbonatite and melilitite-carbonatite tuffs. It is proposed that the carbonatite ash was originally of alkali carbonate composition and that the alkali component was dissolved, leaving a residuum of calcium carbonate. The least recrystallized melilitite-carbonatite tuff contains early-deposited calcite cement and calcite pseudomorphs after nyerereite (?) that have contents of strontium and barium and ??18O and ??13C values suggestive of incomplete chemical and isotopic exchange during alteration and replacement of alkali carbonatite ash. Carbonatite tuffs of the Kaiserstuhl contain globules composed of calcite phenocrysts and microphenocrysts in a groundmass of calcite with a small amount of clay, apatite, and magnetite. The SrO contents of phenocrysts, microphenocrysts, and groundmass calcite average 0.90, 1.42, and 0.59 percent, respectively. The average ??18O and ??13C values of globules (+14.3 and -9.0, respectively) fall between those of coarse-grained intrusive Kaiserstuhl carbonatite (avg. +6.6, -5.8) and those of low-temperature calcite cement in the carbonatite tuffs (+21.8, -14.9). The phenocrysts and microphenocrysts are primary magmatic calcite, but several features indicate that the groundmass has been recrystallized and altered in contact with meteoric water, resulting in weathering of silicate to clay, leaching of strontium, and isotopic exchange. The weight of evidence favors an original high content of alkali carbonatite in the groundmass, with recrystallization following leaching of the alkalies. ?? 1983 Springer-Verlag.

Activated and Micronized Zeolite in the Modulation of Cellular Oxidative Stress in Mexican Smokers: A Randomized Clinical Trial.

PubMed

Atitlán-Gil, Alfonso; Bretón-de la Loza, Martín M; Jiménez-Ortega, José C; Belefant-Miller, Helen; Betanzos-Cabrera, Gabriel

2017-01-01

Activated and micronized zeolites are used as detoxifying agents in humans. Detoxification is attributed to their ability to reduce lipid peroxidation by scavenging free radicals. To evaluate activated and micronized zeolites as modulators of cellular oxidative stress in Mexican smokers without lung diseases. Randomized clinical trial. Subjects were randomly divided into three groups: activated and micronized zeolites, n = 29; vitamin E, an accepted antioxidant, n = 29; and maltodextrin as control, n = 27. Each group received the corresponding supplementation, dissolved in water, once a day for 30 days as follows: activated and micronized zeolites, 5.4 g activated and micronized zeolite; vitamin E, 400 mg D-alpha tocopheryl acetate; and maltodextrin, 250 mg of maltodextrin. The thiobarbituric acid reactive substances assay was used to screen for lipid peroxidation. Catalase activity, plasma antioxidant capacity, and hydrogen peroxide levels were also measured. Results were analyzed by a one-way ANOVA and post hoc test of Bonferroni. Subjects administered activated and micronized zeolites had equivalent antioxidant activities as subjects administered vitamin E. Activated and micronized zeolites may be useful as a modulator of oxidative stress in smokers. However, inclusion of a comparison group of non-smokers would be useful in future studies to assess the degree to which zeolites reverse the oxidant stress.

Zeolites in the Pine Ridge Indian Reservation, South Dakota

USGS Publications Warehouse

Raymond, William H.; Bush, Alfred L.; Gude, Arthur J.

1982-01-01

Zeolites of possible commercial value occur in the Brule Formation of Oligocene age and the Sharps Formation (Harksen, 1961) of Miocene age which crop out in a wide area in the northern part of the Pine Ridge Indian Reservation. The thickness of the zeolite-bearing Interval and the extent of areas within the Interval which contain significant amounts of zeolites are far greater than was expected prior to this investigation. The shape of the zeolite-bearing Interval is tabular and the dimensions of Its exposure are roughly 10 ml x 200 mi x 150 ft (16 km x 160 km x 45 m) thick. Within the study area, there are tracts in which the zeolite resource potential is significant (see pl. 2). This report is intended to inform the Oglala Sioux Tribe of some of the most promising zeolite occurrences. Initial steps can then be taken by the Tribe toward possible development of the resources, should they wish to do so. The data contained herein identify areas of high zeolite potential, but are not adequate to establish economic value for the deposits. If development is recommended by the tribal government, we suggest that the tribal government contact companies involved in research and production of natural zeolites and provide them with the data in this report.

In-situ aging microwave heating synthesis of LTA zeolite layer on mesoporous TiO2 coated porous alumina support

NASA Astrophysics Data System (ADS)

Baig, Mirza A.; Patel, Faheemuddin; Alhooshani, Khalid; Muraza, Oki; Wang, Evelyn N.; Laoui, Tahar

2015-12-01

LTA zeolite layer was successfully grown on a superhydrophilic mesoporous titania layer coated onto porous α-alumina substrate. Mesoporous titania layer was formed as an intermediate bridge in the pore size variation between the macroporous α-alumina support and micro-porous LTA zeolite layer. In-situ aging microwave heating synthesis method was utilized to deposit the LTA zeolite layer. Mesoporous titania layer was pre-treated with UV photons and this was observed to have played a major role in improving the surface hydrophilicity of the substrate leading to formation of increased number of Ti-OH groups on the surface. This increase in Ti-OH groups enhanced the interaction between the synthesis gel and the substrate leading to strong attachment of the amorphous gel on the substrate, thus enhancing coverage of the LTA zeolite layer to almost the entire surface of the 1-inch (25.4 mm) diameter membrane. LTA zeolite layer was developed via in-situ aged under microwave irradiation to study the effect of synthesis parameters such as in-situ aging time and synthesis time on the formation of the LTA zeolite layer. Optimized process parameters resulted in the formation of crack-free porous zeolite layer yielding a zeolite-titania-alumina multi-layer membrane with a gradient in porosity.

Pioneering In Situ Recrystallization during Bead Milling: A Top-down Approach to Prepare Zeolite A Nanocrystals.

PubMed

Anand, Chokkalingam; Yamaguchi, Yudai; Liu, Zhendong; Ibe, Sayoko; Elangovan, Shanmugam P; Ishii, Toshihiro; Ishikawa, Tsuyoshi; Endo, Akira; Okubo, Tatsuya; Wakihara, Toru

2016-07-05

Top-down approach has been viewed as an efficient and straightforward method to prepare nanosized zeolites. Yet, the mechanical breaking of zeolite causes amorphization, which usually requires a post-milling recrystallization to obtain fully crystalline nanoparticles. Herein we present a facile methodology to prepare zeolite nanocrystals, where milling and recrystallization can be performed in situ. A milling apparatus specially designed to work under conditions of high alkalinity and temperature enables the in situ recrystallization during milling. Taking zeolite A as an example, we demonstrate its size reduction from ~3 μm to 66 nm in 30 min, which is quite faster than previous methods reported. Three functions, viz., miniaturization, amorphization and recrystallization were found to take effect concurrently during this one-pot process. The dynamic balance between these three functions was achieved by adjusting the milling period and temperature, which lead to the tuning of zeolite A particle size. Particle size and crystallinity of the zeolite A nanocrystals were confirmed by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and water adsorption-desorption. This work presents a pioneering advancement in this field of nanosized zeolites, and will facilitate the mass production as well as boost the wide applications of nanosized zeolites.

Pioneering In Situ Recrystallization during Bead Milling: A Top-down Approach to Prepare Zeolite A Nanocrystals

PubMed Central

Anand, Chokkalingam; Yamaguchi, Yudai; Liu, Zhendong; Ibe, Sayoko; Elangovan, Shanmugam P.; Ishii, Toshihiro; Ishikawa, Tsuyoshi; Endo, Akira; Okubo, Tatsuya; Wakihara, Toru

2016-01-01

Top-down approach has been viewed as an efficient and straightforward method to prepare nanosized zeolites. Yet, the mechanical breaking of zeolite causes amorphization, which usually requires a post-milling recrystallization to obtain fully crystalline nanoparticles. Herein we present a facile methodology to prepare zeolite nanocrystals, where milling and recrystallization can be performed in situ. A milling apparatus specially designed to work under conditions of high alkalinity and temperature enables the in situ recrystallization during milling. Taking zeolite A as an example, we demonstrate its size reduction from ~3 μm to 66 nm in 30 min, which is quite faster than previous methods reported. Three functions, viz., miniaturization, amorphization and recrystallization were found to take effect concurrently during this one-pot process. The dynamic balance between these three functions was achieved by adjusting the milling period and temperature, which lead to the tuning of zeolite A particle size. Particle size and crystallinity of the zeolite A nanocrystals were confirmed by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and water adsorption-desorption. This work presents a pioneering advancement in this field of nanosized zeolites, and will facilitate the mass production as well as boost the wide applications of nanosized zeolites. PMID:27378145

Theoretical Investigation of Methane Hydroxylation over Isoelectronic [FeO]2+- and [MnO]+-Exchanged Zeolites Activated by N2O.

PubMed

Mahyuddin, M Haris; Shiota, Yoshihito; Staykov, Aleksandar; Yoshizawa, Kazunari

2017-09-05

While the most likely structure of the active site in iron-containing zeolites has been recently identified as [FeO] 2+ (Snyder et al. Nature 2016, 536, 317-321), the mechanism for the direct conversion of methane to methanol over this active species is still debatable between the direct-radical-rebound or nonradical (concerted) mechanism. Using density functional theory on periodic systems, we calculated the two reaction mechanisms over two d 4 isoelectronic systems, [FeO] 2+ and [MnO] + zeolites. We found that [FeO] 2+ zeolites favor the direct-radical-rebound mechanism with low CH 4 activation energies, while [MnO] + zeolites prefer the nonradical mechanism with higher CH 4 activation energies. These contrasts, despite their isoelectronic structures, are mainly due to the differences in the metal coordination number and O α (oxo) spin density. Moreover, molecular orbital analyses suggest that the zeolite steric hindrance further degrades the reactivity of [MnO] + zeolites toward methane. Two types of zeolite frameworks, i.e., medium-pore ZSM-5 (MFI framework) and small-pore SSZ-39 (AEI framework) zeolites, were evaluated, but no significant differences in the reactivity were found. The rate-determining reaction step is found to be methanol desorption instead of methane activation. Careful examination of the most stable sites hosting the active species and calculation for N 2 O decomposition over [Fe] 2+ -MFI and -AEI zeolites were also performed.

Adsorption and photocatalytic degradation of pharmaceuticals and pesticides by carbon doped-TiO2 coated on zeolites under solar light irradiation.

PubMed

An, Ye; de Ridder, David Johannes; Zhao, Chun; Schoutteten, Klaas; Bussche, Julie Vanden; Zheng, Huaili; Chen, Gang; Vanhaecke, Lynn

2016-01-01

To evaluate the performance of zeolite-supported carbon-doped TiO(2) composite catalysts toward target pollutants under solar light irradiation, the adsorption and photocatalytic degradation of 18 pharmaceuticals and pesticides with distinguishing features (molecular size and volume, and photolysis) were investigated using mordenite zeolites with SiO(2)/Al(2)O(3) ratios of 18 and 240. Different quantities of carbon-doped TiO(2) were coated on the zeolites, and then the finished composite catalysts were tested in demineralized, surface, and hospital wastewater samples, respectively. The composite photocatalysts were characterized by X-ray diffraction, field emission scanning electron microscopy, and surface area and porosity analyses. Results showed that a dispersed layer of carbon-doped TiO(2) is formed on the zeolite surface; this layer blocks the micropores of zeolites and reduces their surface area. However, these reductions did not significantly affect adsorption onto the zeolites. Our results demonstrated that zeolite-supported carbon-doped TiO(2) systems can effectively degrade 18 pharmaceuticals and pesticides in demineralized water under natural and simulated solar light irradiation. In surface and hospital wastewaters, zeolite-supported carbon-doped TiO(2) systems present excellent anti-interference capability against radical scavengers and competitive organics for pollutants removal, and higher pollutants adsorption on zeolites evidently enhances the removal rate of target pollutants in surface and hospital wastewater samples with a complicated matrix.

Experimental study on the adsorptive-distillation for dehydration of ethanol-water mixture using natural and synthetic zeolites

NASA Astrophysics Data System (ADS)

Megawati, Wicaksono, D.; Abdullah, M. S.

2017-03-01

This research studied adsorptive-distillation (AD) for dehydration of ethanol-water mixture using natural and synthetic zeolites as adsorbent for ethanol purification. Especially, the effect of purification time is recorded and studied to evaluate performance of designed AD equipment. This AD was performed in a batch condition using boiling flask covered with heating mantle and it was maintained at 78°C temperature and 1 atm pressure. The initial ethanol volume was 300 mL with 93.8% v/v concentration. The synthetic zeolite type used was zeolite 3A. The flowed vapour was condensed using water as a cooling medium. Every 5 minutes of time duration the samples were collected until the vapour could not be condensed in that condition and then be analyzed its concentration using Gas-Chromatography. Experiment shows that the designed AD equipment could increase ethanol concentration at first 5 minutes with highest ethanol concentration achieved using synthetic zeolite (97.47% v/v). However, ethanol concentration from AD process using natural zeolite only reached 96.5% v/v. Thus, synthetic zeolite as adsorbent could pass azeotropic point, but natural zeolite fail. The ratio of adsorbed water per adsorbent for natural and synthetic zeolites are about 0.023 and 0.056 gwater/gads, respectively, at 50 minutes of time. Finally, synthetic zeolite (at 55 minutes the value of C/C0 is about 0.85 and the average outlet water concentration is 4.70 mole/L) as adsorbent for AD of ethanol water is better than natural zeolite (at 55 minutes the value of C/C0 is about 0.63 and the average outlet water concentration is 6.43 mole/L).

Magnetic zeolite NaA: synthesis, characterization based on metakaolin and its application for the removal of Cu2+, Pb2+.

PubMed

Liu, Haibo; Peng, Shuchuan; Shu, Lin; Chen, Tianhu; Bao, Teng; Frost, Ray L

2013-06-01

The optimum parameters for synthesis of zeolite NaA based on metakaolin were investigated according to results of cation exchange capacity and static water adsorption of all synthesis products and selected X-ray diffraction (XRD). Magnetic zeolite NaA was synthesized by adding Fe3O4 in the precursor of zeolite. Zeolite NaA and magnetic zeolite NaA were characterized with scanning electron microscopy (SEM) and XRD. Magnetic zeolite NaA with different Fe3O4 loadings was prepared and used for removal of heavy metals (Cu(2+), Pb(2+)). The results show the optimum parameters for synthesis zeolite NaA are SiO2/Al2O3=2.3, Na2O/SiO2=1.4, H2O/Na2O=50, crystallization time 8h, crystallization temperature 95 °C. The addition of Fe3O4 makes the NaA zeolite with good magnetic susceptibility and good magnetic stability regardless of the Fe3O4 loading, confirming the considerable separation efficiency. Additionally, Fe3O4 loading had a little effect on removal of heavy metal by magnetic zeolite, however, the adsorption capacity still reaches 2.3 mmol g(-1) for Cu(2+), Pb(2+) with a removal efficiency of over 95% in spite of 4.7% Fe3O4 loading. This indicates magnetic zeolite can be used to remove metal heavy at least Cu(2+), Pb(2+) from water with metallic contaminants and can be separated easily after a magnetic process. Copyright © 2013 Elsevier Ltd. All rights reserved.

Modification of zeolite 4A for use as an adsorbent for glyphosate and as an antibacterial agent for water.

PubMed

Zavareh, Siamak; Farrokhzad, Zahra; Darvishi, Farshad

2018-07-15

The aim of this work was to design a low cost adsorbent for efficient and selective removal of glyphosate from water at neutral pH conditions. For this purpose, zeolite 4A, a locally abundant and cheap mineral material, was ion-exchanged with Cu 2+ to produce Cu-zeolite 4A. The FTIR results revealed that the modification has no important effect on chemical structure of zeolite 4A. After modification, highly crystalline zeolite 4A was converted to amorphous Cu-zeolite 4A according to XRD studies. The SEM images showed spherical-like particles with porous surfaces for Cu-zeolite 4A compared to cubic particles with smooth surfaces for zeolite 4A. Adsorption equilibrium data were well fitted with non-linear forms of Langmuir, Freundlich and Temkin isotherms. The maximum adsorption capacity for Cu-zeolite 4A was calculated to be 112.7 mg g -1 based on the Langmuir model. The adsorption of glyphosate by the modified adsorbent had fast kinetics fitted both pseudo-first-order and pseudo-second-order models. A mechanism based on chemical adsorption was proposed for the removal process. The modified adsorbent had a good selectivity to glyphosate over natural waters common cations and anions. It also showed desired regeneration ability as an important feature for practical uses. The potential use of the developed material as antibacterial agent for water disinfection filters was also investigated by MIC method. Relatively strong antibacterial activity was observed for Cu-zeolite 4A against Gram-positive and Gram-negative model bacteria while zeolite 4A had no antibacterial properties. No release of Cu 2+ to aqueous solutions was detected as unique feature of the developed material. Copyright © 2018 Elsevier Inc. All rights reserved.

Applications of zeolites in biotechnology and medicine - a review.

PubMed

Bacakova, Lucie; Vandrovcova, Marta; Kopova, Ivana; Jirka, Ivan

2018-05-01

Zeolites are microporous tectosilicates of natural or synthetic origin, which have been extensively used in various technological applications, e.g. as catalysts and as molecular sieves, for separating and sorting various molecules, for water and air purification, including removal of radioactive contaminants, for harvesting waste heat and solar heat energy, for adsorption refrigeration, as detergents, etc. These applications of zeolites were typically related with their porous character, their high adsorption capacity, and their ion exchange properties. This review is focused on potential or already practically implemented applications of zeolites in biotechnology and medicine. Zeolites are promising for environment protection, detoxication of animal and human organisms, improvement of the nutrition status and immunity of farm animals, separation of various biomolecules and cells, construction of biosensors and detection of biomarkers of various diseases, controlled drug and gene delivery, radical scavenging, and particularly tissue engineering and biomaterial coating. As components of scaffolds for bone tissue engineering, zeolites can deliver oxygen to cells, can stimulate osteogenic cell differentiation, and can inhibit bone resorption. Zeolites can also act as oxygen reservoirs, and can improve cell performance in vascular and skin tissue engineering and wound healing. When deposited on metallic materials for bone implantation, zeolite films showed anticorrosion effects, and improved the osseointegration of these implants. In our studies, silicalite-1 films deposited on silicon or stainless steel substrates improved the adhesion, growth, viability and osteogenic differentiation of human osteoblast-like Saos-2 cells. Zeolites have been clinically used as components of haemostatics, e.g. in the Advanced Clotting Sponge, as gastroprotective drugs, e.g. Absorbatox® 2.4D, or as antioxidative agents (Klinobind®). Some zeolites are highly cytotoxic and carcinogenic, e.g. erionite. However, in other zeolites, the antiproliferative and pro-apoptotic effects can be used for tumor therapy.

Supported Rhenium Complexes: Almost Uniform Rhenium Tricarbonyls Synthesized from CH[subscript 3]Re(CO)[subscript 5] and HY Zeolite

DOE Office of Scientific and Technical Information (OSTI.GOV)

Lobo-Lapidus, Rodrigo J.; Gates, Bruce C.

2010-12-07

Supported rhenium complexes were prepared from CH{sub 3}Re(CO){sub 5} and dealuminated HY zeolite or NaY zeolite, each with a Si/Al atomic ratio of 30. The samples were characterized with infrared (IR) and extended X-ray absorption fine structure (EXAFS) spectroscopies. EXAFS data characterizing the sample formed by the reaction of CH{sub 3}Re(CO){sub 5} with dealuminated HY zeolite show that the rhenium complexes were bonded to the zeolite frame, incorporating, on average, three carbonyl ligands per Re atom (as shown by Re-C and multiple-scattering Re-O EXAFS contributions). The IR spectra, consistent with this result, show that the supported rhenium carbonyls were bondedmore » near aluminum sites of the zeolite, as shown by the decrease in intensity of the IR bands characterizing the acidic silanol groups resulting from the reaction of the rhenium carbonyl with the zeolite. This supported metal complex was characterized by narrow peaks in the {nu}{sub CO} region of the IR spectrum, indicating highly uniform species. In contrast, the species formed from CH{sub 3}Re(CO){sub 5} on NaY zeolite lost fewer carbonyl ligands than those formed on HY zeolite and were significantly less uniform, as indicated by the greater breadth of the {nu}{sub CO} bands in the IR spectra. The results show the importance of zeolite H{sup +} sites for the formation of uniform supported rhenium carbonyls from CH{sub 3}Re(CO){sub 5}; the formation of such uniform complexes did not occur on the NaY zeolite.« less

Pore-water extraction from unsaturated tuff by triaxial and one-dimensional compression methods, Nevada Test Site, Nevada

DOE Office of Scientific and Technical Information (OSTI.GOV)

Mower, T.E.; Higgins, J.D.; Yang, In C.

1994-07-01

The hydrologic system in the unsaturated tuff at Yucca Mountain, Nevada, is being evaluated for the US Department of Energy by the Yucca Mountain Project Branch of the US Geological Survey as a potential site for a high-level radioactive-waste repository. Part of this investigation includes a hydrochemical study that is being made to assess characteristics of the hydrologic system such as: traveltime, direction of flow, recharge and source relations, and types and magnitudes of chemical reactions in the unsaturated tuff. In addition, this hydrochemical information will be used in the study of the dispersive and corrosive effects of unsaturated-zone watermore » on the radioactive-waste storage canisters. This report describes the design and validation of laboratory experimental procedures for extracting representative samples of uncontaminated pore water from welded and nonwelded, unsaturated tuffs from the Nevada Test Site.« less

Effect of the addition of by-product ash of date palms on the mechanical characteristics of gypsum-calcareous materials used in road construction

NASA Astrophysics Data System (ADS)

Khellou, A.; Kriker, A.; Hafssi, A.; Belbarka, K.; Baali, K.

2016-07-01

The gypsum-calcareous materials, also known as the crusting tuff, are used in the pavement layers of low -traffic road and considered as the materials of first choice in the Saharan region of Algeria. The objective of this paper is to study the mechanical characteristics of tuff of Ouargla town that is situated in the Southeast of Algeria, by adding different percentage of ash resulted from the combustion of by-products of date palms, such as 4%, 8% and l2%, to the tuff. The results obtained have shown a remarkable improvement both in compressive strength at different ages and in the bearing index in the two cases immediate and after immersion in water. These characteristics of the mixture (tuff+ash) reach their maximum values at the 8% of ash addition.

Hierarchical zeolites from class F coal fly ash

NASA Astrophysics Data System (ADS)

Chitta, Pallavi

Fly ash, a coal combustion byproduct is classified as types class C and class F. Class C fly ash is traditionally recycled for concrete applications and Class F fly ash often disposed in landfills. Class F poses an environmental hazard due to disposal and leaching of heavy metals into ground water and is important to be recycled in order to mitigate the environmental challenges. A major recycling option is to reuse the fly ash as a low-cost raw material for the production of crystalline zeolites, which serve as catalysts, detergents and adsorbents in the chemical industry. Most of the prior literature of fly ash conversion to zeolites does not focus on creating high zeolite surface area zeolites specifically with hierarchical pore structure, which are very important properties in developing a heterogeneous catalyst for catalysis applications. This research work aids in the development of an economical process for the synthesis of high surface area hierarchical zeolites from class F coal fly ash. In this work, synthesis of zeolites from fly ash using classic hydrothermal treatment approach and fusion pretreatment approach were examined. The fusion pretreatment method led to higher extent of dissolution of silica from quartz and mullite phases, which in turn led to higher surface area and pore size of the zeolite. A qualitative kinetic model developed here attributes the difference in silica content to Si/Al ratio of the beginning fraction of fly ash. At near ambient crystallization temperatures and longer crystallization times, the zeolite formed is a hierarchical faujasite with high surface area of at least 360 m2/g. This work enables the large scale recycling of class F coal fly ash to produce zeolites and mitigate environmental concerns. Design of experiments was used to predict surface area and pore sizes of zeolites - thus obviating the need for intense experimentation. The hierarchical zeolite catalyst supports tested for CO2 conversion, yielded hydrocarbons up to C9, a performance attesting the hierarchal pore structure. The preliminary techno-economic feasibility assessment demonstrates a net energy saving of 75% and cost saving of 63% compared to the commercial zeolite manufacturing process.

[Effect of Nano Zeolite on Chemical Fractions of Cd in Soil and Its Uptake by Cabbage].

PubMed

Xiong, Shi-juan; Xu, Wei-hong; Xie, Wen-wen; Chen, Rong; Chen, Yong-qin; Chi, Sun-lin; Chen, Xu- gen; Zhang, Jin-zhong; Xiong, Zhi-ting; Wang, Zheng-yin; Xie, De-ti

2015-12-01

Incubation experiments were carried out to investigate the influence of different nano zeolite (NZ) and ordinary zeolite (OZ) levels(0, 5, 10 and 20 g · kg⁻¹) on the change trends in fraction distribution coefficient (FDC) of Cd when exposed to different Cadmium (Cd) levels (1, 5, 10 and 15 mg · kg⁻¹), and pot experiments were carried out to investigate their influence on soil Cd fraction and Cd uptake by cabbage. The results in incubation experiments showed that the application of nano zeolite as well as ordinary zeolite effectively decreased the FDC of exchangeable Cd and increased the FDC of Fe-Mn oxide fraction. The FDC of soil Cd from 0 d to 28 d was deceased at first, then increased and tended to be stable, and finally increased. At the end of incubation, the FDC of soil exchangeable Cd decreased from 72.0%-88.0% to 30.0%-66.4%. Exchangeable fraction Cd was the most dominant Cd fraction in soil during the whole incubation. The results in pot experiment indicated that the application of nano zeolite and ordinary zeolite decreased the concentration and FDC of soil exchangeable Cd, and concurrently the concentration and FDC of Cd in carbonate, Fe-Mn oxide, organic matter and residual fraction were increased. The lowest EX-Cd was observed in the treatment with high dose of nano zeolite (20 g · kg⁻¹). The FDC of exchangeable Cd showed significant negative relationship with the soil pH (P < 0.05), and was concurrently extremely positively correlated with Cd concentration in shoot and root of cabbage (P < 0.01). Soil pH increased by 1.8%-45.5% and 6.1%-54.3% in the presence of zeolite when exposed to 5 mg · kg⁻¹ 1 and Cd, respectively; FDC of exchangeable Cd decreased by 16.3%-47.7% and 16.2%-46.7%; Cd concentration in each tissues of cabbage decreased by 1.0%-75.0% and 3.8%-53.2%, respectively. Moreover, the reduction effect of nano zeolite on soil and plant Cd was better than that of ordinary zeolite. The growth of cabbage was stimulated by low and medium zeolite doses (≤ 10 g · kg⁻¹), while inhibited by high zeolite doses (20 g · kg⁻¹). Compared to ordinary zeolite, the biomass of Chinese cabbage was significantly increased by Nano zeolite, while the exchangeable Cd in soil as well as Cd concentration and Cd accumulation of cabbage were significantly reduced.

The age and composition of the pre-Cenozoic basement of the Jalisco Block: implications for and relation to the Guerrero composite terrane

NASA Astrophysics Data System (ADS)

Valencia, Victor A.; Righter, Kevin; Rosas-Elguera, Jose; López-Martínez, Margarita; Grove, Marty

2013-09-01

The Jalisco Block is thought to be part of the Guerrero terrane, but the nature and age of the underlying crystalline basement are largely unknown. We have collected a suite of schists, granitoids, and weakly metamorphosed marine sediments from various parts of the Jalisco Block including Atenguillo and Ameca, Mascota and San Sebastián, Cuale, Puerto Vallarta, Punta Mita, Yelapa, and Tomatlán. The schists range in age from 135 to 161 Ma, with many exhibiting Proterozoic and Phanerozoic zircon ages. The granitoids range in age from 65 to 90 Ma, and are calc-alkaline compositionally—similar to granitoids from the Puerto Vallarta and Los Cabos batholiths. The Jalisco granitoids also experienced similar uplift rates to granitoids from the regions to the north and south of the Jalisco Block. The marine sediments yield a maximum depositional age of 131 Ma, and also contain a significant zircon population with ages extending back to the Archean. Granitoids from this study define two age groups, even after the effects of thermal resetting and different closure temperatures are considered. The 66.8-Ma silicic ash flow tuff near Union de Tula significantly expands the extent of this Cretaceous-Paleocene age ash flow tuff unit within the Jalisco Block, and we propose calling the unit "Carmichael silicic ash flow tuff volcanic succession" in honor of Ian Carmichael. The ages of the basement schists in the Jalisco Block fully overlap with the ages of terranes of continental Mexico, and other parts of the Guerrero terrane in the south, confirming the autochthonous origin of the Jalisco Block rather than exotic arc or allochthonous origin. Geologic data, in combination with geochronologic and oxygen isotopic data, suggest the evolution of SW Mexico with an early 200-1,200-Ma passive margin, followed by steep subduction in a continental arc setting at 160-165 Ma, then shallower subduction by 135 Ma, and finally, emplacement of granitoids at 65-90 Ma.

Catalytic Oxidation by Transition Metal Ions in Zeolites.

DTIC Science & Technology

1984-09-28

exotic schemes were developed. It was previously demonstrated that MoCI5 may be reacted with a HYu (here Yu denotes a steam-stabilized or...34ultrastable" zeolite) to form a MoYu zeolite and HC1 which is removed from the system.1 In this study, MoYu zeolites have been prepared by reacting HYu with Mo

Framework Stabilization of Si-Rich LTA Zeolite Prepared in Organic-Free Media

DOE Office of Scientific and Technical Information (OSTI.GOV)

Conato, Marlon T.; Oleksiak, Matthew D.; McGrail, B. Peter

2014-10-16

Zeolite HOU-2 (LTA type) is prepared with the highest silica content (Si/Al = 2.1) reported for Na-LTA zeolites without the use of an organic structure-directing agent. The rational design of Si-rich zeolites has the potential to improve their thermal stability for applications in catalysis, gas storage, and selective separations.

PEG-template for surface modification of zeolite: A convenient material to the design of polypropylene based composite for packaging films

NASA Astrophysics Data System (ADS)

Toommee, S.; Pratumpong, P.

2018-06-01

Zeolite was successfully modified by conventional synthetic route. Polyethylene glycol was employed for surface modification of zeolite. The surface of zeolite exhibited therefore hydrophobic properties. Less than 5 wt% of modified zeolites with uniform size and shape were integrated into polypropylene matrix. Mechanical properties of composite exhibited the similar trend compare to neat polypropylene. Oxygen transmission rate and water vapor transmission rate were evaluated and it exhibited the strong potential to be a good candidate material in active packaging.

Method for the recovery of silver from silver zeolite

DOEpatents

Reimann, G.A.

1985-03-05

High purity silver is recovered from silver exchanged zeolite used to capture radioactive iodine from nuclear reactor and nuclear fuel reprocessing environments. The silver exchanged zeolite is heated with slag formers to melt and fluidize the zeolite and release the silver, the radioactivity removing with the slag. The silver containing metallic impurities is remelted and treated with oxygen and a flux to remove the metal impurities. About 98% of the silver in the silver exchanged zeolite having a purity of 99% or better is recoverable by the method.

Method for the recovery of silver from silver zeolite

DOEpatents

Reimann, George A.

1986-01-01

High purity silver is recovered from silver exchanged zeolite used to capture radioactive iodine from nuclear reactor and nuclear fuel reprocessing environments. The silver exchanged zeolite is heated with slag formers to melt and fluidize the zeolite and release the silver, the radioactivity removing with the slag. The silver containing metallic impurities is remelted and treated with oxygen and a flux to remove the metal impurities. About 98% of the silver in the silver exchanged zeolite having a purity of 99% or better is recoverable by the method.

Zeolite Crystal Growth in Microgravity and on Earth

NASA Technical Reports Server (NTRS)

2003-01-01

The Center for Advanced Microgravity Materials Processing (CAMMP), a NASA-sponsored Research Partnership Center, is working to improve zeolite materials for storing hydrogen fuel. CAMMP is also applying zeolites to detergents, optical cables, gas and vapor detection for environmental monitoring and control, and chemical production techniques that significantly reduce by-products that are hazardous to the environment. Shown here are zeolite crystals (top) grown in a ground control experiment and grown in microgravity on the USML-2 mission (bottom). Zeolite experiments have also been conducted aboard the International Space Station.

On the reactive occlusion of the (uranium trichloride + lithium chloride + potassium chloride) eutectic salt in zeolite 4A

NASA Astrophysics Data System (ADS)

Lexa, Dusan; Leibowitz, Leonard; Kropf, Jeremy

2000-03-01

The interaction between the (uranium trichloride + lithium chloride + potassium chloride) eutectic salt and zeolite 4A has been studied by temperature-resolved synchrotron powder X-ray diffraction, evolved gas analysis and differential scanning calorimetry, between 300 and 900 K. The onset of salt occlusion by the zeolite has been detected at 450 K. Evidence of a reaction between zeolitic water and uranium trichloride, leading to the formation of uranium dioxide, has appeared at 600 K. The uranium dioxide particle size increases from 2 nm at 600 K to 25 nm at 900 K - an indication of their extra-zeolitic location. No appreciable degradation of the zeolite structure has been observed.

Measurement of cation exchange capacity (CEC) on natural zeolite by percolation method

NASA Astrophysics Data System (ADS)

Wiyantoko, Bayu; Rahmah, Nafisa

2017-12-01

The cation exchange capacity (CEC)measurement has been carried out in natural zeolite by percolation method. The natural zeolite samples used for cation exchange capacity measurement were activated beforehand with physical activation and chemical activation. The physically activated zeolite was done by calcination process at 600 °C for 4 hours. The natural zeolite was activated chemically by using sodium hydroxide by refluxing process at 60-80 °C for 3 hours. In summary, cation exchange capacity (CEC) determination was performed by percolation, distillation and titration processes. Based on the measurement that has been done, the exchange rate results from physical activated and chemical activated of natural zeolite were 181.90cmol (+)/kg and 901.49cmol (+)/kg respectively.

Synthesis and characterization of mesoporous NaY zeolite from natural Blitar’s kaolin

NASA Astrophysics Data System (ADS)

Khalifah, S. N.; aini, Z. N.; Hayati, E. K.; Aini, N.; Prasetyo, A.

2018-03-01

Mesoporous NaY Zeolite has been synthesized from calcined natural Blitar’s kaolin with the addition of NaOH and CTABr surfactant as mesoporous template by hydrothermal method. Natural kaolin was calcinated with different time and temperature to change kaolin to metakaolin. X-ray diffraction data showed that mesoporous NaY zeolite was formed with impurities compound of sodalite, kaolin and quartz phases. The BET analysis resulted that the pore of NaY Zeolite belongs to mesoporous type with pore size 9,421 nm. Characterization from FTIR confirmed about the functional group of zeolites (988, 776, 663, 464 cm-1). Scanning electron microscopy characterization showed that the morphological of mesoporous NaY zeolites have uniform and crystalline particles formed.

Synthesis of Zeolite-X from Bottom Ash for H2 Adsorption

NASA Astrophysics Data System (ADS)

Kurniawan, R. Y.; Romadiansyah, T. Q.; Tsamarah, A. D.; Widiastuti, N.

2018-01-01

Zeolite-X was synthesized from bottom ash power plant waste using fusion method on air atmosphere. The fused product dissolved in demineralized water and aluminate solution was added to adjust the SiO2/Al2O3 molar ratio gel prior hydrothermal process. The synthesis results were characterized using X-Ray Diffraction (XRD), Scanning Electron Microscope (SEM), and Fourier Transform Infrared (FTIR). The results showed that the zeolite-X has a high crystallinity with octahedral particle. The pure-form zeolite-X then was characterized and tested for H2 gas adsorption by gravimetric method to determine the H2 gas adsorption capacity of zeolite-X from bottom ash and it was compared to synthetic zeolite-X.

Major element and oxygen isotope geochemistry of vapour-phase garnet from the Topopah Spring Tuff at Yucca Mountain, Nevada, USA

USGS Publications Warehouse

Moscati, Richard J.; Johnson, Craig A.

2014-01-01

Twenty vapour-phase garnets were studied in two samples of the Topopah Spring Tuff of the Paintbrush Group from Yucca Mountain, in southern Nevada. The Miocene-age Topopah Spring Tuff is a 350 m thick, devitrified, moderately to densely welded ash-flow tuff that is zoned compositionally from high-silica rhyolite to latite. During cooling of the tuff, escaping vapour produced lithophysae (former gas cavities) lined with an assemblage of tridymite (commonly inverted to cristobalite or quartz), sanidine and locally, hematite and/or garnet. Vapour-phase topaz and economic deposits associated commonly with topaz-bearing rhyolites (characteristically enriched in F) were not found in the Topopah Spring Tuff at Yucca Mountain. Based on their occurrence only in lithophysae, the garnets are not primary igneous phenocrysts, but rather crystals that grew from a F-poor magma-derived vapour trapped during and after emplacement of the tuff. The garnets are euhedral, vitreous, reddish brown, trapezohedral, as large as 2 mm in diameter and fractured. The garnets also contain inclusions of tridymite. Electron microprobe analyses of the garnets reveal that they are almandine-spessartine (48.0 and 47.9 mol.%, respectively), have an average composition of (Fe1.46Mn1.45Mg0.03Ca0.10)(Al1.93Ti0.02)Si3.01O12 and are comparatively homogeneous in Fe and Mn concentrations from core to rim. Composited garnets from each sample site have δ18O values of 7.2 and 7.4‰. The associated quartz (after tridymite) has δ18O values of 17.4 and 17.6‰, values indicative of reaction with later, low-temperature water. Unaltered tridymite from higher in the stratigraphic section has a δ18O of 11.1‰ which, when coupled with the garnet δ18O values in a quartz-garnet fractionation equation, indicates isotopic equilibration (vapour-phase crystallization) at temperatures of ~600°C. This high-temperature mineralization, formed during cooling of the tuffs, is distinct from the later and commonly recognized low-temperature stage (generally 50–70°C) of calcite, quartz and opal secondary mineralization, formed from downward-percolating meteoric water, that locally coats fracture footwalls and lithophysal floors.

A high-pyrite semianthracite of Late Permian age in the Songzao Coalfield, southwestern China: Mineralogical and geochemical relations with underlying mafic tuffs

USGS Publications Warehouse

Dai, S.; Wang, X.; Chen, W.; Li, D.; Chou, C.-L.; Zhou, Y.; Zhu, Chen; Li, H.; Zhu, Xudong; Xing, Y.; Zhang, W.; Zou, J.

2010-01-01

The No. 12 Coal (Late Permian) in the Songzao Coalfield, Chongqing, southwestern China, is characteristically high in pyrite and some trace elements. It is uniquely deposited directly above mafic tuff beds. Samples of coal and tuffs have been studied for their mineralogy and geochemistry using inductively coupled plasma-mass spectrometry, X-ray fluorescence, plasma low-temperature ashing plus powder X-ray diffraction, and scanning electron microscopy equipped with energy-dispersive X-ray analysis.The results show that the minerals of the No. 12 Coal are mainly composed of pyrite, clay minerals (kaolinite, chamosite, and illite), ankerite, calcite, and trace amounts of quartz and boehmite. Kaolinite and boehmite were mainly derived from sediment source region of mafic tuffs. Chamosite was formed by the reaction of kaolinite with Fe-Mg-rich fluids during early diagenesis. The high pyrite (Sp,d=8.83%) in the coal was related to marine transgression over peat deposits and abundant Fe derived from the underlying mafic tuff bed. Ankerite and calcite were precipitated from epigenetic fluids.Chemical compositions of incompatible elements indicate that the tuffs were derived from enriched mantle and the source magmas had an alkali-basalt character. Compared to other coals from the Songzao Coalfield and common Chinese coals, the No. 12 Coal has a lower SiO2/Al2O3 (1.13) but a higher Al2O3/Na2O (80.1) value and is significantly enriched in trace elements including Sc (13.5??g/g), V (121??g/g), Cr (33.6??g/g), Co (27.2??g/g), Ni (83.5??g/g), Cu (48.5??g/g), Ga (17.3??g/g), Y (68.3??g/g), Zr (444??g/g), Nb (23.8??g/g), and REE (392??g/g on average). Above mineralogical compositions, as well as similar ratios of selected elements (e.g., SiO2/Al2O3 and Al2O3/Na2O) and similar distribution patterns of incompatible elements (e.g., the mantle-normalized diagram for incompatible elements and chondrite-normalized diagram for rare earth elements) of coal and tuff, indicated that enriched trace elements above were largely derived from mafic tuffs, in addition to a minor amount from the Kandian Oldland. ?? 2010 Elsevier B.V.

Tertiary volcanic rocks and uranium in the Thomas Range and northern Drum Mountains, Juab County, Utah

USGS Publications Warehouse

Lindsey, David A.

1982-01-01

The Thomas Range and northern Drum Mountains have a history of volcanism, faulting, and mineralization that began about 42 m.y. (million years) ago. Volcanic activity and mineralization in the area can be divided into three stages according to the time-related occurrence of rock types, trace-element associations, and chemical composition of mineral deposits. Compositions of volcanic rocks changed abruptly from rhyodacite-quartz latite (42-39 m.y. ago) to rhyolite (38-32 m.y. ago) to alkali rhyolite (21 and 6-7 m.y. ago); these stages correspond to periods of chalcophile and siderophile metal mineralization, no mineralization(?), and lithophile metal mineralization, respectively. Angular unconformities record episodes of cauldron collapse and block faulting between the stages of volcanic activity and mineralization. The youngest angular unconformity formed between 21 and 7 m.y. ago during basin-and-range faulting. Early rhyodacite-quartz latite volcanism from composite volcanoes and fissures produced flows, breccias, and ash-flow tuff of the Drum Mountains Rhyodacite and Mt. Laird Tuff. Eruption of the Mt. Laird Tuff about 39 m.y. ago from an area north of Joy townsite was accompanied by collapse of the Thomas caldera. Part of the roof of the magma chamber did not collapse, or the magma was resurgent, as is indicated by porphyry dikes and plugs in the Drum Mountains. Chalcophile and siderophile metal mineralization, resulting in deposits of copper, gold, and manganese, accompanied early volcanism. Te middle stage of volcanic activity was characterized by explosive eruption of rhyolitic ash-flow tuffs and collapse of the Dugway Valley cauldron. Eruption of the Joy Tuff 38 m.y. ago was accompanied by subsidence of this cauldron and was followed by collapse and sliding of Paleozoic rocks from the west wall of the cauldron. Landslides in The Dell were covered by the Dell Tuff, erupted 32 m.y. ago from an unknown source to the east. An ash flow of the Needles Range(?) Formation was erupted 30-31 m.y. ago from an unknown source. Mineralization probably did not occur during the rhyolitic stage of volcanism. The last stage of volcanism was contemporaneous with basin-and-range faulting and was characterized by explosive eruption of ash and pumice, forming stratified tuff, and by quiet eruption of alkali rhyolite as viscous flows and domes. The first episode of alkali rhyolite volcanism deposited the beryllium tuff and porphyritic rhyolite members of the Spor Mountain Formation 21 m.y. ago. After a period of block faulting, the stratified tuff and alkali rhyolite of the Topaz Mountain Rhyolite were erupted 6-7 m.y. ago along faults and fault intersections. Erosion of Spor Mountain, as well as explosive eruptions through dolomite, provided abundant dolomite detritus to the beryllium tuff member. The alkali rhyolite of both formations is fluorine rich, as is evident from abundant topaz, and contains anomalous amounts of lithophile metals. Alkali rhyolite volcanism was accompanied by lithophile metal mineralization which deposited fluorite, beryllium, and uranium. The structure of the area is dominated by the Thomas caldera and the younger Dugway Valley cauldron, which is nested within the Thomas caldera; the Thomas caldera is surrounded by a rim of Paleozoic rocks at Spor Mountain and Paleozoic to Precambrian rocks in the Drum Mountains. The Joy fault and Dell fault system mark the ring-fracture zone of the Thomas caldera. These structural features began to form about 39 m.y. ago during eruption of the Mt. Laird Tuff and caldera subsidence. The Dugway Valley cauldron sank along a series of steplike normal faults southeast of Topaz Mountain in response to collapse of the magma chamber of the Joy Tuff. Caldera structure was modified by block faulting between 21 and 7 m.y. ago, the time of widespread extensional faulting in the Basin and Range Province. Vents erupted alkali rhyolite 6-7 m.y. ago along basin-and-range faults.

Effect of Fe3O4 addition on removal of ammonium by zeolite NaA.

PubMed

Liu, Haibo; Peng, Shuchuan; Shu, Lin; Chen, Tianhu; Bao, Teng; Frost, Ray L

2013-01-15

Magnetic zeolite NaA with different Fe(3)O(4) loadings was prepared by hydrothermal synthesis based on metakaolin and Fe(3)O(4). The effect of added Fe(3)O(4) on the removal of ammonium by zeolite NaA was investigated by varying the Fe(3)O(4) loading, pH, adsorption temperature, initial concentration, adsorption time. Langmuir, Freundlich, and pseudo-second-order modeling were used to describe the nature and mechanism of ammonium ion exchange using both zeolite and magnetic zeolite. Thermodynamic parameters such as change in Gibbs free energy, enthalpy and entropy were calculated. The results show that all the selected factors affect the ammonium ion exchange by zeolite and magnetic zeolite, however, the added Fe(3)O(4) apparently does not affect the ion exchange performance of zeolite to the ammonium ion. Freundlich model provides a better description of the adsorption process than Langmuir model. Moreover, kinetic analysis indicates the exchange of ammonium on the two materials follows a pseudo-second-order model. Thermodynamic analysis makes it clear that the adsorption process of ammonium is spontaneous and exothermic. Regardless of kinetic or thermodynamic analysis, all the results suggest that no considerable effect on the adsorption of the ammonium ion by zeolite is found after the addition of Fe(3)O(4). According to the results, magnetic zeolite NaA can be used for the removal of ammonium due to the good adsorption performance and easy separation method from aqueous solution. Copyright © 2012 Elsevier Inc. All rights reserved.

Scaling Relations for Acidity and Reactivity of Zeolites

PubMed Central

2017-01-01

Zeolites are widely applied as solid acid catalysts in various technological processes. In this work we have computationally investigated how catalytic reactivity scales with acidity for a range of zeolites with different topologies and chemical compositions. We found that straightforward correlations are limited to zeolites with the same topology. The adsorption energies of bases such as carbon monoxide (CO), acetonitrile (CH3CN), ammonia (NH3), trimethylamine (N(CH3)3), and pyridine (C5H5N) give the same trend of acid strength for FAU zeolites with varying composition. Crystal orbital Hamilton populations (COHP) analysis provides a detailed molecular orbital picture of adsorbed base molecules on the Brønsted acid sites (BAS). Bonding is dominated by strong σ donation from guest molecules to the BAS for the adsorbed CO and CH3CN complexes. An electronic descriptor of acid strength is constructed based on the bond order calculations, which is an intrinsic parameter rather than adsorption energy that contains additional contributions due to secondary effects such as van der Waals interactions with the zeolite walls. The bond order parameter derived for the CH3CN adsorption complex represents a useful descriptor for the intrinsic acid strength of FAU zeolites. For FAU zeolites the activation energy for the conversion of π-adsorbed isobutene into alkoxy species correlates well with the acid strength determined by the NH3 adsorption energies. Other zeolites such as MFI and CHA do not follow the scaling relations obtained for FAU; we ascribe this to the different van der Waals interactions and steric effects induced by zeolite framework topology. PMID:29142616

Preparation of highly stable zeolite-alginate foam composite for strontium(90Sr) removal from seawater and evaluation of Sr adsorption performance.

PubMed

Hong, Hye-Jin; Kim, Byoung-Gyu; Ryu, Jungho; Park, In-Su; Chung, Kang-Sup; Lee, Sang Moon; Lee, Jin-Bae; Jeong, Hyeon Su; Kim, Hyunchul; Ryu, Taegong

2018-01-01

Alginate bead is a promising strontium (Sr) adsorbent in seawater, but highly concentrated Na ions caused over-swelling and damaged the hydrogel bead. To improve the mechanical stability of alginate bead, flexible foam-type zeolite-alginate composite was synthesized and Sr adsorption performance was evaluated in seawater; 1-10% zeolite immobilized alginate foams were prepared by freeze-dry technique. Immobilization of zeolite into alginate foam converted macro-pores to meso-pores which lead to more compact structure. It resulted in less swollen composite in seawater medium and exhibited highly improved mechanical stability compared with alginate bead. Besides, Sr adsorption efficiency and selectivity were enhanced by immobilization of zeolite in alginate foam due to the increase of Sr binding sites (zeolite). In particular, Sr selectivity against Na was highly improved. The 10% zeolite-alginate foam exhibited a higher log K d of 3.3, while the pure alginate foam exhibited 2.7 in the presence of 0.1 M Na. Finally, in the real seawater, the 10% zeolite-alginate foam exhibited 1.5 times higher Sr adsorption efficiency than the pure alginate foam. This result reveals that zeolite-alginate foam composite is appropriate material for Sr removal in seawater due to its swelling resistance as well as improved Sr adsorption performance in complex media. Copyright © 2017 Elsevier Ltd. All rights reserved.

Synthesis of Engineered Zeolitic Materials: From Classical Zeolites to Hierarchical Core-Shell Materials.

PubMed

Masoumifard, Nima; Guillet-Nicolas, Rémy; Kleitz, Freddy

2018-04-01

The term "engineered zeolitic materials" refers to a class of materials with a rationally designed pore system and active-sites distribution. They are primarily made of crystalline microporous zeolites as the main building blocks, which can be accompanied by other secondary components to form composite materials. These materials are of potential importance in many industrial fields like catalysis or selective adsorption. Herein, critical aspects related to the synthesis and modification of such materials are discussed. The first section provides a short introduction on classical zeolite structures and properties, and their conventional synthesis methods. Then, the motivating rationale behind the growing demand for structural alteration of these zeolitic materials is discussed, with an emphasis on the ongoing struggles regarding mass-transfer issues. The state-of-the-art techniques that are currently available for overcoming these hurdles are reviewed. Following this, the focus is set on core-shell composites as one of the promising pathways toward the creation of a new generation of highly versatile and efficient engineered zeolitic substances. The synthesis approaches developed thus far to make zeolitic core-shell materials and their analogues, yolk-shell, and hollow materials, are also examined and summarized. Finally, the last section concisely reviews the performance of novel core-shell, yolk-shell, and hollow zeolitic materials for some important industrial applications. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Impact of steel slag on the ammonium adsorption by zeolite and a new configuration of zeolite-steel slag substrate for constructed wetlands.

PubMed

Shi, Pengbo; Jiang, Yingbo; Zhu, Hongtao; Sun, Dezhi

2017-07-01

The CaO dissolution from slag, as well as the effects of influencing parameters (i.e. pH and Ca 2+ concentration) on the ammonium adsorption onto zeolite, was systematically studied in this paper. Modeling results of Ca 2+ and OH - release from slag indicated that pseudo-second-order reaction had a better fitness than pseudo-first-order reaction. Changing pH value from 7 to 12 resulted in a drastic reduction of the ammonium adsorption capacity on zeolite, from the peak adsorption capacity at pH 7. High Ca 2+ concentration in solution also inhibited the adsorption of ammonium onto zeolite. There are two proposed mechanisms for steel slag inhibiting the ammonium adsorption capacity of zeolite. On the one hand, OH - released from steel slag can react with ammonium ions to produce the molecular form of ammonia (NH 3 ·H 2 O), which would cause the dissociation of NH 4 + from zeolite. On the other hand, Ca 2+ could replace the NH 4 + ions to adhere onto the surface of zeolite. An innovative substrate filling configuration with zeolite placed upstream of the steel slag was then proposed to eliminate the disadvantageous effects of steel slag. Experimental results showed that this novel filling configuration was superior to two other filling configurations in terms of ammonium removal.

Zeolites in Eocene basaltic pillow lavas of the Siletz River Volcanics, Central Coast Range, Oregon

USGS Publications Warehouse

Keith, Terry E.C.; Staplese, Lloyd W.

1985-01-01

Zeolites and associated minerals occur in a tholeiitic basaltic pillow lava sequence that makes up part of the Eocene Siletz River Volcanics in the central Coast Range, Oregon. Regional zoning of zeolite assemblages is not apparent; the zeolites formed in joints, fractures, and interstices, although most occur in central cavities of basalt pillows. The zeolites and associated minerals identified, in general order of paragenetic sequence, are smectite, pyrite, calcite (small spheres), thomsonite, natrolite, analcime, scolecite, mesolite, stilbite, heulandite, apophyllite, chahazite, mordenite, calcite (scalenohedra and twinned rhombohedra), laumontite, and amethystine quartz. Common three-mineral assemblages are: natrolite-analcime-sfilbite, stilbite-heulandite-chabazite, stilbite-apophyllie-chabazite, and natrolite-mesolite-laumontite.Alteration of basaltic glass, which was initially abundant, appears to have been an important factor in formation of the zeolites. Isotopic data suggest that zeolitization occurred during a low-temperature (60 ~ 70°C submarine hydrothermal event, or by reactions of cold (~ 10°C meteoric water with basalt over a long time. The occurrence of different mineral assemblages in cavities of adjacent basalt pillows indicates that these minerals crystallized in dosed systems that were isolated as fractures and joints were sealed by deposition of smectite and early zeolites. Although the total chemical composition of the mineral assemblages in cavities is similar, different mineral species formed because of the sensitivity of zeolite minerals to slight variations in physical and chemical conditions within individual cavities.

Immobilizing of catalyst using Bayah's natural zeolite to reduce the chemical oxygen demand (COD) and total organic carbon (TOC)

NASA Astrophysics Data System (ADS)

Jayanudin, Kustiningsih, Indar; Sari, Denni Kartika

2017-05-01

Indonesia is rich of natural minerals, many of which had not been widely used. One potential natural mineral is zeolite from Bayah Banten that can be used to support catalyst in the process of waste degradation. The purpose of this research is to characterize the Bayah's zeolite and to figure out the effectiveness of the zeolite as supporting agent to the Fe catalyst in the process of phenol degradation, with the main purposes are to reduce the Chemical Oxygen Demand (COD) and Total Organic Carbon (TOC). This research consists of three steps, activation of natural zeolite using 1M, 2M, and 3M NaOH solution, impregnation process with 0.025M, 0.05 M and 0.075M Fe(NO3)3.9H2O solution, and calcination at 500°C. Bayah's natural zeolite was characterize using Brauner-Emmet-Teller (BET) for its pore area, X-ray Fluorescence (XRF) for analyzing zeolite's component before and after activation process and after impregnation process, and Scanning Electron Microscope (SEM) for analyzing zeolite's morphology. The result showed that the highest pore area was 9Å, Fe metal from Fe(NO3)3.9H2O 0,075 M solution remained in zeolite pore was 7,73%, the reduction of COD and TOC was yielded at H2O2: phenol ratio of 1 : 6.

Erionite and other fibrous zeolites in volcanic environments: the need for a risk assessment in Italy

NASA Astrophysics Data System (ADS)

Cavallo, A.; Rimoldi, B.

2012-04-01

In many European countries in the '90s there was a significant increase in mortality linked to mesothelioma, a cancer of the lung, involving pleural, pericardial and peritoneal mesothelial cells, which unfortunately has no cure at present. Though most of these cases have been attributed to t asbestos, in Italy at least 17% of cases of mesothelioma is still not fully explained. In the years between 1990 and 2000, it was discovered that the inhalation of erionite fibers (a zeolite group mineral, that can be found in altered volcanic rocks) was the cause of a regional epidemic of mesothelioma in some villages of Cappadocia (Turkey). Erionite, in fact, was recently included in Class 1 (highly carcinogenic) by the World Health Organization, up to 800 times more carcinogenic than asbestos; on the other hand, little is known about the toxicity of other fibrous zeolites, commonly intergrown with erionite, such as offretite and mordenite. Erionite was reported in different regions of Italy; nevertheless, a systematic mapping of its distribution, the quantification of its presence in rocks and data about airborne fibers are still missing. We carried out first preliminary sampling in Veneto, in Tertiary volcanic rocks, mainly hydrothermally altered basalts. The first mineralogical investigations by means of XRPD, SEM-EDS and OM confirmed the presence of small amounts of erionite and abundant fibrous offretite, in vugs of basaltic rocks. Intergrowths and overgrowths with other fibrous minerals are quite common, and the morphological-chemical similarities among these zeolites pose a special analytical problem, with the need of combining different techniques. Our first findings, combined with the fact that zeolites are important industrial minerals, emphasize the need of a risk assessment in Italy and Europe, because there are no systematic studies on the distribution of erionite or similar fibrous zeolites in the environment. The knowledge of the epidemiology of mesothelioma linked to erionite in Italy is extremely scarce: INAIL, through its database of occupational diseases, can provide essential information for epidemiological research. An effective risk assessment in Italy will require coordinated actions from government agencies, local health authorities, Universities and research centers, in order to record the actual presence of fibrous zeolites, recognizing mineral species and quantifying their abundance in rock deposits. The different geological conditions through time of volcanic deposits will be compared with an updated "database" on the physical-chemical-geological conditions of formation of zeolites. In sites where the presence of fibrous zeolites has been validated by laboratory tests, we will proceed with accurate field surveys and sampling campaigns, in order to determine detailed geological-stratigraphic and structural features, and resolving precisely the thickness, areal extent and volume of lithostratigraphic units containing these minerals. These data will be entered into a GIS to produce a result that can be used immediately and in the long-period by research institutes, local authorities and regional agencies for environmental protection. In sites where the presence of hazardous fibrous minerals has been validated, we will plan airborne fibers sampling campaigns, and we will assess the extent of airborne dispersion produced by natural agents and by man activity. In the case that these sites host active mining or quarrying activities, we will quantify the airborne fibers contamination at workplaces and propose measures for environmental risk mitigation.

Influence of different natural zeolite concentrations on the anaerobic digestion of piggery waste.

PubMed

Milán, Z; Sánchez, E; Weiland, P; Borja, R; Martín, A; Ilangovan, K

2001-10-01

The effect of different natural zeolite concentrations on the anaerobic digestion of piggery waste was studied. Natural zeolite doses in the range 0.2-10 g/l of wastewater were used in batch experiments, which were carried out at temperatures between 27 degrees C and 30 degrees C. Total chemical oxygen demand (COD), total and volatile solids, ammonia and organic nitrogen, pH, total volatile fatty acids (TVFA), alkalinity (Alk) and accumulative methane production were determined during 30 days of digestion. The anaerobic digestion process was favored by the addition of natural zeolite at doses between 2 and 4 g/l and increasingly inhibited at doses beyond 6 g/l. A first-order kinetic model of COD removal was used to determine the apparent kinetic constants of the process. The kinetic constant values increased with the zeolite amount up to a concentration of 4 g/l. The values of the maximum accumulative methane production (Gm) increased until zeolite concentrations of 2-4 g/l. The addition of zeolite reduced the values of the TVFA/ Alk ratio while increasing the pH values, and these facts could contribute to the process failure at zeolite doses of 10 g/l.

Properties and applications of zeolites.

PubMed

Rhodes, Christopher J

2010-01-01

Zeolites are aluminosilicate solids bearing a negatively charged honeycomb framework of micropores into which molecules may be adsorbed for environmental decontamination, and to catalyse chemical reactions. They are central to green-chemistry since the necessity for organic solvents is minimised. Proton-exchanged (H) zeolites are extensively employed in the petrochemical industry for cracking crude oil fractions into fuels and chemical feedstocks for other industrial processes. Due to their ability to perform cation-exchange, in which the cations that are originally present to counterbalance the framework negative charge may be exchanged out of the zeolite by cations present in aqueous solution, zeolites are useful as industrial water-softeners, in the removal of radioactive Cs+ and Sr2+ cations from liquid nuclear waste and in the removal of toxic heavy metal cations from groundwaters and run-off waters. Surfactant-modified zeolites (SMZ) find particular application in the co-removal of both toxic anions and organic pollutants. Toxic anions such as arsenite, arsenate, chromate, cyanide and radioactive iodide can also be removed by adsorption into zeolites that have been previously loaded with co-precipitating metal cations such as Ag+ and Pb2+ which form practically insoluble complexes that are contained within the zeolite matrix.

Shear Rheology of Suspensions of Porous Zeolite Particles in Concentrated Polymer Solutions

NASA Astrophysics Data System (ADS)

Olanrewaju, Kayode O.; Breedveld, Victor

2008-07-01

We present experimental data on the shear rheology of Ultem (polyetherimide)/NMP(l-methyl-2-pyrrolidinone) solutions with and without suspended surface-modified porous/nonporous zeolite (ZSM-5) particles. We found that the porous zeolite suspensions have relative viscosities that significantly exceed the Krieger-Dougherty predictions for hard sphere suspensions. The major origin of this discrepancy is the selective absorption of NMP solvent into the zeolite pores, which raises both the polymer concentration and the particle volume fraction, thus enhancing both the viscosity of the continuous phase Ultem/NMP polymer solution and the particle contribution to the suspension viscosity. Other factors, such as zeolite non-sphericity and specific interactions with Ultem polymer, contribute to the suspension viscosity to a lesser extent. We propose a predictive model for the viscosity of porous zeolite suspensions by incorporating an absorption parameter, α, into the Krieger-Dougherty model. We also propose independent approaches to determine α. The first one is indirect and based on zeolite density/porosity data, assuming that all pores will be filled with solvent. The other method is based on our experimental data, by comparing the viscosity data of porous versus non-porous zeolite suspensions. The different approaches are compared.

Zeolites: Can they be synthesized by design

DOE Office of Scientific and Technical Information (OSTI.GOV)

Davis, M.E.

1994-09-01

Zeolites and zeolite-like molecular sieves are crystalline oxides that have high surface-to-volume ratios and are able to recognize, discriminate, and organize molecules with differences of < 1 [angstrom]. The close connection between the atomic structure and macroscopic properties of these materials has led to uses in molecular recognition. For example, zeolites and zeolite-like molecular sieves can reveal marvelous molecular recognition specificity and sensitivity that can be applied to catalysis, separations technology, and chemical sensing. Additionally, they can serve as hosts to organize guest atoms and molecules that endow composite materials with optoelectric and electrochemical properties. Because of the high levelmore » of structural control necessary to create high-performance materials with zeolites or zeolite-like molecular sieves, the design and synthesis of these solids with specific architectures and properties are highly desired. Although this lofty goal is still elusive, advances have been made to allow the serious consideration of designing molecular sieves. Here, the author covers two aspects of this ongoing effort. First, he discusses the feasibility of designing pore architectures through the use of organic structure-directing agents. Second, he explores the possibility of creating zeolites through ''Lego chemistry.''« less

Selective Ring Opening of 1-Methylnaphthalene Over NiW-Supported Catalyst Using Dealuminated Beta Zeolite.

PubMed

Kim, Eun-Sang; Lee, You-Jin; Kim, Jeong-Rang; Kim, Joo-Wan; Kim, Tae-Wan; Chae, Ho-Jeong; Kim, Chul-Ung; Lee, Chang-Ha; Jeong, Soon-Yong

2016-02-01

Nanoporous Beta zeolite was dealuminated by weak acid treatment for reducing the acidity. Bi-functional catalysts were prepared using commercial Beta zeolites and the dealuminated zeolites for acidic function, NiW for metallic function. 1-Methylnaphthalene was selected as a model compound for multi-ring aromatics in heavy oil, and its selective ring opening reaction has been investigated using the prepared bi-functional catalysts with different acidity in fixed bed reaction system. The dealuminated Beta zeolites, which crystal structure and nanoporosity were maintained, showed the higher SiO2/Al2O3 ratio and smaller acidity than their original zeolite. NiW-supported catalyst using the dealuminated Beta zeolite with SiO2/Al203 mole ratio of 55 showed the highest performance for the selective ring opening. The acidity of catalyst seemed to play an important role as active sites for the selective ring opening of 1-methylnaphthalene but there should be some optimum catalyst acidity for the reaction. The acidity of Beta zeolite could be controlled by the acid treatment and the catalyst with the optimum acidity for the selective ring opening could be prepared.

A Fiber Optic Interferometric Sensor Platform for Determining Gas Diffusivity in Zeolite Films.

PubMed

Yang, Ruidong; Xu, Zhi; Zeng, Shixuan; Jing, Wenheng; Trontz, Adam; Dong, Junhang

2018-04-04

Fiber optic interferometer (FOI) sensors have been fabricated by directly growing pure-silica MFI-type zeolite (i.e., silicalite) films on straight-cut endfaces of single-mode communication optical fibers. The FOI sensor has been demonstrated for determining molecular diffusivity in the zeolite by monitoring the temporal response of light interference from the zeolite film during the dynamic process of gas adsorption. The optical thickness of the zeolite film depends on the amount of gas adsorption that causes the light interference to shift upon loading molecules into the zeolitic channels. Thus, the time-dependence of the optical signal reflected from the coated zeolite film can represent the adsorption uptake curve, which allows computation of the diffusivity using models derived from the Fick’s Law equations. In this study, the diffusivity of isobutane in silicalite has been determined by the new FOI sensing method, and the results are in good agreement with literature values obtained by various conventional macroscopic techniques. The FOI sensor platform, because of its robustness and small size, could be useful for studying molecular diffusion in zeolitic materials under conditions that are inaccessible to the existing techniques.

Atmospheric Pressure Plasma Jet-Assisted Synthesis of Zeolite-Based Low-k Thin Films.

PubMed

Huang, Kai-Yu; Chi, Heng-Yu; Kao, Peng-Kai; Huang, Fei-Hung; Jian, Qi-Ming; Cheng, I-Chun; Lee, Wen-Ya; Hsu, Cheng-Che; Kang, Dun-Yen

2018-01-10

Zeolites are ideal low-dielectric constant (low-k) materials. This paper reports on a novel plasma-assisted approach to the synthesis of low-k thin films comprising pure-silica zeolite MFI. The proposed method involves treating the aged solution using an atmospheric pressure plasma jet (APPJ). The high reactivity of the resulting nitrogen plasma helps to produce zeolite crystals with high crystallinity and uniform crystal size distribution. The APPJ treatment also remarkably reduces the time for hydrothermal reaction. The zeolite MFI suspensions synthesized with the APPJ treatment are used for the wet deposition to form thin films. The deposited zeolite thin films possessed dense morphology and high crystallinity, which overcome the trade-off between crystallinity and film quality. Zeolite thin films synthesized using the proposed APPJ treatment achieve low leakage current (on the order of 10 -8 A/cm 2 ) and high Young's modulus (12 GPa), outperforming the control sample synthesized without plasma treatment. The dielectric constant of our zeolite thin films was as low as 1.41. The overall performance of the low-k thin films synthesized with the APPJ treatment far exceed existing low-k films comprising pure-silica MFI.

Explosive shaped charge penetration into tuff rock

DOE Office of Scientific and Technical Information (OSTI.GOV)

Vigil, M.G.

1988-10-01

Analysis and data for the use of Explosive Shaped Charges (ESC) to generate holes in tuff rock formation is presented. The ESCs evaluated include Conical Shaped Charges (CSC) and Explosive Formed Projectiles (EFP). The CSCs vary in size from 0.158 to 9.1 inches inside cone diameter. The EFPs were 5.0 inches in diameter. Data for projectile impact angles of 30 and 90 degrees are presented. Analytically predicted depth of penetration data generally compared favorably with experimental data. Predicted depth of penetration versus ESC standoff data and hole profile dimensions in tuff are also presented. 24 refs., 45 figs., 6 tabs.

(40)Ar/(39)Ar dating of Bed I, Olduvai Gorge, Tanzania, and the chronology of early Pleistocene climate change.

PubMed

Deino, Alan L

2012-08-01

(40)Ar/(39)Ar dating of tuffs and lavas of the late Pleistocene volcanic and sedimentary sequence of Olduvai Gorge, north-central Tanzania, provides the basis for a revision of Bed I chronostratigraphy. Bed I extends from immediately above the Naabi Ignimbrite at 2.038 ± 0.005 Ma to Tuff IF at 1.803 ± 0.002 Ma. Tuff IB, a prominent widespread marker tuff in the basin and a key to understanding hominin evolutionary chronologies and paleoclimate histories, has an age of 1.848 ± 0.003 Ma. The largest lake expansion event in the closed Olduvai lake basin during Bed I times encompassed the episode of eruption and emplacement of this tuff. This lake event is nearly coincident with the maximum precessional insolation peak of the entire Bed I/Lower Bed II interval, calculated from an astronomical model of the boreal summer orbital insolation time-series. The succeeding precessional peak also apparently coincides with the next youngest expansion of paleo-Lake Olduvai. The extreme wet/dry climate shifts seen in the upper part of Bed I occur during an Earth-orbital eccentricity maximum, similar to episodic lake expansions documented elsewhere in the East African Rift during the Neogene. Copyright © 2012 Elsevier Ltd. All rights reserved.

Analysis of Conservative Tracer Tests in the Bullfrog, Tram, and Prow Pass Tuffs, 1996 to 1998, Yucca Mountain, Nye County, Nevada

USGS Publications Warehouse

Umari, Amjad; Fahy, Michael F.; Earle, John D.; Tucci, Patrick

2008-01-01

To evaluate the potential for transport of radionuclides in ground water from the proposed high-level nuclear-waste repository at Yucca Mountain, Nevada, conservative (nonsorbing) tracer tests were conducted among three boreholes, known as the C-hole Complex, and values for transport (or flow) porosity, storage (or matrix) porosity, longitudinal dispersivity, and the extent of matrix diffusion were obtained. The C-holes are completed in a sequence of Miocene tuffaceous rock, consisting of nonwelded to densely welded ash-flow tuff with intervals of ash-fall tuff and volcaniclastic rocks, covered by Quaternary alluvium. The lower part of the tuffaceous-rock sequence includes the Prow Pass, Bullfrog, and Tram Tuffs of the Crater Flat Group. The rocks are pervaded by tectonic and cooling fractures. Paleozoic limestone and dolomite underlie the tuffaceous rocks. Four radially convergent and one partially recirculating conservative (nonsorbing) tracer tests were conducted at the C-hole Complex from 1996 to 1998 to establish values for flow porosity, storage porosity, longitudinal dispersivity, and extent of matrix diffusion in the Bullfrog and Tram Tuffs and the Prow Pass Tuff. Tracer tests included (1) injection of iodide into the combined Bullfrog-Tram interval; (2) injection of 2,6 difluorobenzoic acid into the Lower Bullfrog interval; (3) injection of 3-carbamoyl-2-pyridone into the Lower Bullfrog interval; and (4) injection of iodide and 2,4,5 trifluorobenzoic acid, followed by 2,3,4,5 tetrafluorobenzoic acid, into the Prow Pass Tuff. All tracer tests were analyzed by the Moench single- and dual-porosity analytical solutions to the advection-dispersion equation or by superposition of these solutions. Nonlinear regression techniques were used to corroborate tracer solution results, to obtain optimal parameter values from the solutions, and to quantify parameter uncertainty resulting from analyzing two of the three radially convergent conservative tracer tests conducted in the Bullfrog and Tram intervals. Longitudinal dispersivity values in the Bullfrog and Tram Tuffs ranged from 1.83 to 2.6 meters, flow-porosity values from 0.072 to 0.099, and matrix-porosity values from 0.088 to 0.19. The flow-porosity values indicate that the pathways between boreholes UE-25 c#2 and UE-25 c#3 in the Bullfrog and Tram intervals are not connected well. Tracer testing in the Prow Pass interval indicates different transport characteristics than those obtained in the Bullfrog and Tram intervals. In the Prow Pass Tuff, longitudinal dispersivity was 0.27 meter, flow porosity was 4.5 ? 10?4, and matrix porosity was 0.01. This indicates that the flow network in the Prow Pass is dominated by interconnected fractures, whereas in the Bullfrog and Tram, the flow network is dominated by discontinuous fractures with connecting segments of matrix.

Halloysite nanotube-based electrospun ceramic nanofibre mat: a novel support for zeolite membranes

PubMed Central

Chen, Zhuwen; Zeng, Jiaying; Lv, Dong; Gao, Jinqiang; Zhang, Jian; Bai, Shan; Li, Ruili; Wu, Jingshen

2016-01-01

Some key parameters of supports such as porosity, pore shape and size are of great importance for fabrication and performance of zeolite membranes. In this study, we fabricated millimetre-thick, self-standing electrospun ceramic nanofibre mats and employed them as a novel support for zeolite membranes. The nanofibre mats were prepared by electrospinning a halloysite nanotubes/polyvinyl pyrrolidone composite followed by a programmed sintering process. The interwoven nanofibre mats possess up to 80% porosity, narrow pore size distribution, low pore tortuosity and highly interconnected pore structure. Compared with the commercial α-Al2O3 supports prepared by powder compaction and sintering, the halloysite nanotube-based mats (HNMs) show higher flux, better adsorption of zeolite seeds, adhesion of zeolite membranes and lower Al leaching. Four types of zeolite membranes supported on HNMs have been successfully synthesized with either in situ crystallization or a secondary growth method, demonstrating good universality of HNMs for supporting zeolite membranes. PMID:28083098

Investigation of mircroorganisms colonising activated zeolites during anaerobic biogas production from grass silage.

PubMed

Weiss, S; Zankel, A; Lebuhn, M; Petrak, S; Somitsch, W; Guebitz, G M

2011-03-01

The colonisation of activated zeolites (i.e. clinoptilolites) as carriers for microorganisms involved in the biogas process was investigated. Zeolite particle sizes of 1.0-2.5mm were introduced to anaerobic laboratory batch-cultures and to continuously operated bioreactors during biogas production from grass silage. Incubation over 5-84 days led to the colonisation of zeolite surfaces in small batch-cultures (500 ml) and even in larger scaled and flow-through disturbed bioreactors (28 l). Morphological insights were obtained by using scanning electron microscopy (SEM). Single strand conformation polymorphism (SSCP) analysis based on amplification of bacterial and archaeal 16S rRNA fragments demonstrated structurally distinct populations preferring zeolite as operational environment. via sequence analysis conspicuous bands from SSCP patterns were identified. Populations immobilised on zeolite (e.g. Ruminofilibacter xylanolyticum) showed pronounced hydrolytic enzyme activity (xylanase) shortly after re-incubation in sterilised sludge on model substrate. In addition, the presence of methanogenic archaea on zeolite particles was demonstrated. Copyright © 2010 Elsevier Ltd. All rights reserved.

Study on adsorption of rhodamine B onto Beta zeolites by tuning SiO2/Al2O3 ratio.

PubMed

Cheng, Zhi-Lin; Li, Yan-Xiang; Liu, Zan

2018-02-01

The exploration of the relationship between zeolite composition and adsorption performance favored to facilitate its better application in removal of the hazardous substances from water. The adsorption capacity of rhodamine B (RB) onto Beta zeolite from aqueous solution was reported. The relationship between SiO 2 /Al 2 O 3 ratio and adsorption capacity of Beta zeolite for RB was explored. The structure and physical properties of Beta zeolites with various SiO 2 /Al 2 O 3 ratios were determined by XRD, FTIR, TEM, BET, UV-vis and so on characterizations. The adsorption behavior of rhodamine B onto Beta zeolite matched to Langmuir adsorption isotherm and more suitable description for the adsorption kinetics was a pseudo-second-order reaction model. The maximum adsorption capacity of the as-prepared Beta zeolite with SiO 2 /Al 2 O 3 = 18.4 was up to 27.97mg/g. Copyright © 2017 Elsevier Inc. All rights reserved.

Elimination of Escherichia coli and Salmonella in Clam by Using Zeolite in a Station of Depuration.

PubMed

Gdoura, Morsi; Sellami, Hanen; Khannous, Lamia; Ketata, Najib; Neila, Idriss Ben; Traore, Al Ibrahim; Chekir, Zouhair; Gdoura, Radhouane

2017-09-01

  The application of natural zeolite for water and wastewater treatment has been carried out and is still a promising technique in environmental cleaning processes. Natural zeolite can be used to improve the purification process of clams (Ruditapes decussatus). Thus, our study aimed at improving the clam purification system in order to reduce Escherichia coli and eliminate Salmonella in samples artificially contaminated with this bacterium using a natural zeolite to replace the biological filter. The results showed that zeolite used in a depuration system improved the clam purification process. Moreover, natural zeolite exhibited high performance in the adsorption of bacteria and allowed to reduce the Escherichia coli abundance in 24 h, thus ensuring purified clams conformity with the ISO 16649-3 standard. These results indicate the beneficial effects of using zeolite in the adsorption of bacteria and the reduction in the abundance of Escherichia coli and set the Salmonella from marine organisms.

Potential and challenges of zeolite chemistry in the catalytic conversion of biomass.

PubMed

Ennaert, Thijs; Van Aelst, Joost; Dijkmans, Jan; De Clercq, Rik; Schutyser, Wouter; Dusselier, Michiel; Verboekend, Danny; Sels, Bert F

2016-02-07

Increasing demand for sustainable chemicals and fuels has pushed academia and industry to search for alternative feedstocks replacing crude oil in traditional refineries. As a result, an immense academic attention has focused on the valorisation of biomass (components) and derived intermediates to generate valuable platform chemicals and fuels. Zeolite catalysis plays a distinct role in many of these biomass conversion routes. This contribution emphasizes the progress and potential in zeolite catalysed biomass conversions and relates these to concepts established in existing petrochemical processes. The application of zeolites, equipped with a variety of active sites, in Brønsted acid, Lewis acid, or multifunctional catalysed reactions is discussed and generalised to provide a comprehensive overview. In addition, the feedstock shift from crude oil to biomass involves new challenges in developing fields, like mesoporosity and pore interconnectivity of zeolites and stability of zeolites in liquid phase. Finally, the future challenges and perspectives of zeolites in the processing of biomass conversion are discussed.

Theoretical studies of the nitrogen containing compounds adsorption behavior on Na(I)Y and rare earth exchanged RE(III)Y zeolites.

PubMed

Geng, Wei; Zhang, Haitao; Zhao, Xuefei; Zan, Wenyan; Gao, Xionghou; Yao, Xiaojun

2015-01-01

In this work, the adsorption behavior of nitrogen containing compounds including NH3, pyridine, quinoline, and carbazole on Na(I)Y and rare earth exchanged La(III)Y, Pr(III)Y, Nd(III)Y zeolites was investigated by density functional theory (DFT) calculations. The calculation results demonstrate that rare earth exchanged zeolites have stronger adsorption ability for nitrogen containing compounds than Na(I)Y. Rare earth exchanged zeolites exhibit strongest interaction with quinoline while weakest with carbazole. Nd(III)Y zeolites are found to have strongest adsorption to all the studied nitrogen containing compounds. The analysis of the electronic total charge density and electron orbital overlaps show that nitrogen containing compounds interact with zeolites by π-electrons of the compounds and the exchanged metal atom. Mulliken charge population analysis also proves that adsorption energies are strongly dependent on the charge transfer between the nitrogen containing molecules and exchanged metal atom in the zeolites.

Halloysite nanotube-based electrospun ceramic nanofibre mat: a novel support for zeolite membranes

NASA Astrophysics Data System (ADS)

Chen, Zhuwen; Zeng, Jiaying; Lv, Dong; Gao, Jinqiang; Zhang, Jian; Bai, Shan; Li, Ruili; Hong, Mei; Wu, Jingshen

2016-12-01

Some key parameters of supports such as porosity, pore shape and size are of great importance for fabrication and performance of zeolite membranes. In this study, we fabricated millimetre-thick, self-standing electrospun ceramic nanofibre mats and employed them as a novel support for zeolite membranes. The nanofibre mats were prepared by electrospinning a halloysite nanotubes/polyvinyl pyrrolidone composite followed by a programmed sintering process. The interwoven nanofibre mats possess up to 80% porosity, narrow pore size distribution, low pore tortuosity and highly interconnected pore structure. Compared with the commercial α-Al2O3 supports prepared by powder compaction and sintering, the halloysite nanotube-based mats (HNMs) show higher flux, better adsorption of zeolite seeds, adhesion of zeolite membranes and lower Al leaching. Four types of zeolite membranes supported on HNMs have been successfully synthesized with either in situ crystallization or a secondary growth method, demonstrating good universality of HNMs for supporting zeolite membranes.

Composting domestic sewage sludge with natural zeolites in a rotary drum reactor.

PubMed

Villaseñor, J; Rodríguez, L; Fernández, F J

2011-01-01

This work aimed the influence of zeolites addition on a sludge-straw composting process using a pilot-scale rotary drum reactor. The type and concentration of three commercial natural zeolites were considered: a mordenite and two clinoptilolites (Klinolith and Zeocat). Mordenite caused the greatest carbon removal (58%), while the clinoptilolites halved losses of ammonium. All zeolites removed 100% of Ni, Cr, Pb, and significant amounts (more than 60%) of Cu, Zn and Hg. Zeocat displayed the greatest retention of ammonium and metals, and retention efficiencies increased as Zeocat concentration increased. The addition of 10% Zeocat produced compost compliant with Spanish regulations. Zeolites were separated from the final compost, and leaching studies suggested that zeolites leachates contained very low metals concentrations (<1 mg/kg). Thus, the final compost could be applied directly to soil, or metal-polluted zeolites could be separated from the compost prior to application. The different options have been discussed. Copyright © 2010 Elsevier Ltd. All rights reserved.

Behaviour at high pressure of Rb7NaGa8Si12O40·3H2O (a zeolite with EDI topology): a combined experimental-computational study

NASA Astrophysics Data System (ADS)

Gatta, G. D.; Tabacchi, G.; Fois, E.; Lee, Y.

2016-03-01

The high-pressure behaviour and the P-induced structural evolution of a synthetic zeolite Rb7NaGa8Si12O40·3H2O (with edingtonite-type structure) were investigated both by in situ synchrotron powder diffraction (with a diamond anvil cell and the methanol:ethanol:water = 16:3:1 mixture as pressure-transmitting fluid) up to 3.27 GPa and by ab initio first-principles computational modelling. No evidence of phase transition or penetration of P-fluid molecules was observed within the P-range investigated. The isothermal equation of state was determined; V 0 and K T0 refined with a second-order Birch-Murnaghan equation of state are V 0 = 1311.3(2) Å3 and K T0 = 29.8(7) GPa. The main deformation mechanism (at the atomic scale) in response to the applied pressure is represented by the cooperative rotation of the secondary building units (SBU) about their chain axis (i.e. [001]). The direct consequence of SBU anti-rotation on the zeolitic channels parallel to [001] is the increase in pore ellipticity with pressure, in response to the extension of the major axis and to the contraction of the minor axis of the elliptical channel parallel to [001]. The effect of the applied pressure on the bonding configuration of the extra-framework content is only secondary. A comparison between the P-induced main deformation mechanisms observed in Rb7NaGa8Si12O40·3H2O and those previously found in natural fibrous zeolites is made.

An Introduction to Zeolite Synthesis Using Imidazolium-Based Cations as Organic Structure-Directing Agents.

PubMed

Vinaches, Paloma; Bernardo-Gusmão, Katia; Pergher, Sibele B C

2017-08-06

Zeolite synthesis is a wide area of study with increasing popularity. Several general reviews have already been published, but they did not summarize the study of imidazolium species in zeolite synthesis. Imidazolium derivatives are promising compounds in the search for new zeolites and can be used to help understand the structure-directing role. Nearly 50 different imidazolium cations have already been used, resulting in a variety of zeolitic types, but there are still many derivatives to be studied. In this context, the purpose of this short review is to help researchers starting in this area by summarizing the most important concepts related to imidazolium-based zeolite studies and by presenting a table of recent imidazolium derivatives that have been recently studied to facilitate filling in the knowledge gaps.

A new approach to evaluate natural zeolite ability to sorb lead (Pb) from aqueous solutions

NASA Astrophysics Data System (ADS)

Drosos, Evangelos I. P.; Karapanagioti, Hrissi K.

2013-04-01

Lead (Pb) is a hazardous pollutant commonly found in aquatic ecosystems. Among several methods available, the addition of sorbent amendments to soils or sediments is attractive, since its application is relatively simple, while it can also be cost effective when a low cost and re-usable sorbent is used; e.g. natural zeolites. Zeolites are crystalline aluminosilicates with a three-dimensional structure composed of a set of cavities occupied by large ions and water molecules. Zeolites can accommodate a wide variety of cations, such as Na+, K+, Ca2+, Mg2+, which are rather loosely held and can readily be exchanged for others in an aqueous solution. Natural zeolites are capable of removing cations, such as lead, from aqueous solutions by ion exchange. There is a wide variation in the cation exchange capacity (CEC) of natural zeolites because of the different nature of various zeolites cage structures, natural structural defects, adsorbed ions, and their associated gangue minerals. Naturally occurring zeolites are rarely pure and are contaminated to varying degrees by other minerals, such as clays and feldspars, metals, quartz, or other zeolites as well. These impurities affect the CEC even for samples originated from the same region but from a different source. CEC of the material increases with decreasing impurity content. Potentially exchangeable ions in such impurities do not necessarily participate in ion exchange mechanism, while, in some cases, impurities may additionally block the access to active sites. For zeoliferous rocks having the same percentage of a zeolitic phase, the CEC increases with decreasing Si/Al ratio, as the more Si ions are substituted by Al ions, the more negative the valence of the matrix becomes. Sodium seems to be the most effective exchangeable ion for lead. On the contrary, it is unlikely that the potassium content of the zeolite would be substituted. A pretreatment with high concentration solutions of Na, such as 2 M NaCl, can significantly improve zeolite CEC by bringing the material to near homoionic form. pH and temperature are the critical parameters for using natural zeolites as sorbents. Zeolites should not be used in extremely acidic, neither in extremely basic pH conditions, except for very short times. The exchange of Pb, requires low solution pH, to avoid precipitation but not too low because the H+ are competitive ions for ion exchange; as a result the zeolite CEC related to Pb removal may be downgraded. If pH enters the basic range (e.g. pH>8), more aquatic complexes with lower positive valence than those prevailing in lower pH are produced; these complexes are less attracted by the negative charged zeolitic matrix. Pb uptake is favored at higher temperatures as ion exchange (including the diffusion of exchangeable ions inside the material and the medium, and vice versa) is an endothermic process. With the increase of temperature there is a decrease in hydration of all available exchangeable cations that eases the movement within the channels of the solid matrix. Additionally, the mobility of the potassium ions, present in the zeolitic material, also increases with the temperature resulting in enhanced CEC.

Chlorine-36 data at Yucca Mountain: Statistical tests of conceptual models for unsaturated-zone flow

USGS Publications Warehouse

Campbell, K.; Wolfsberg, A.; Fabryka-Martin, J.; Sweetkind, D.

2003-01-01

An extensive set of chlorine-36 (36Cl) data has been collected in the Exploratory Studies Facility (ESF), an 8-km-long tunnel at Yucca Mountain, Nevada, for the purpose of developing and testing conceptual models of flow and transport in the unsaturated zone (UZ) at this site. At several locations, the measured values of 36Cl/Cl ratios for salts leached from rock samples are high enough to provide strong evidence that at least a small component of bomb-pulse 36Cl, fallout from atmospheric testing of nuclear devices in the 1950s and 1960s, was measured, implying that some fraction of the water traveled from the ground surface through 200-300 m of unsaturated rock to the level of the ESF during the last 50 years. These data are analyzed here using a formal statistical approach based on log-linear models to evaluate alternative conceptual models for the distribution of such fast flow paths. The most significant determinant of the presence of bomb-pulse 36Cl in a sample from the welded Topopah Spring unit (TSw) is the structural setting from which the sample was collected. Our analysis generally supports the conceptual model that a fault that cuts through the nonwelded Paintbrush tuff unit (PTn) that overlies the TSw is required in order for bomb-pulse 36Cl to be transmitted to the sample depth in less than 50 years. Away from PTn-cutting faults, the ages of water samples at the ESF appear to be a strong function of the thickness of the nonwelded tuff between the ground surface and the ESF, due to slow matrix flow in that unit. ?? 2002 Elsevier Science B.V. All rights reserved.

Volcaniclastic dykes tell on fracturing, explosive eruption and lateral collapse at Stromboli volcano (Italy)

NASA Astrophysics Data System (ADS)

Vezzoli, Luigina; Corazzato, Claudia

2016-05-01

In the upper part of the Stromboli volcano, in the Le Croci and Bastimento areas, two dyke-like bodies of volcanic breccia up to two-metre thick crosscut and intrude the products of Vancori and Neostromboli volcanoes. We describe the lithofacies association of these unusual volcaniclastic dykes, interpret the setting of dyke-forming fractures and the emplacement mechanism of internal deposits, and discuss their probable relationships with the explosive eruption and major lateral collapse events that occurred at the end of the Neostromboli period. The dyke volcaniclastic deposits contain juvenile magmatic fragments (pyroclasts) suggesting a primary volcanic origin. Their petrographic characteristics are coincident with the Neostromboli products. The architecture of the infilling deposits comprises symmetrically-nested volcaniclastic units, separated by sub-vertical boundaries, which are parallel to the dyke margins. The volcanic units are composed of distinctive lithofacies. The more external facies is composed of fine and coarse ash showing sub-vertical laminations, parallel to the contact wall. The central facies comprises stratified, lithic-rich breccia and lapilli-tuff, whose stratification is sub-horizontal and convolute, discordant to the dyke margins. Only at Le Croci dyke, the final unit shows a massive tuff-breccia facies. The volcaniclastic dykes experienced a polyphasic geological evolution comprising three stages. The first phase consisted in fracturing, explosive intrusion related to magma rising and upward injection of magmatic fluids and pyroclasts. The second phase recorded the dilation of fractures and their role as pyroclastic conduits in an explosive eruption possibly coeval with the lateral collapse of the Neostromboli lava cone. Finally, in the third phase, the immediately post-eruption mass-flow remobilization of pyroclastic deposits took place on the volcano slopes.

Physical and stable-isotope evidence for formation of secondary calcite and silica in the unsaturated zone, Yucca Mountain, Nevada

USGS Publications Warehouse

Whelan, J.F.; Paces, J.B.; Peterman, Z.E.

2002-01-01

Calcite and silica form coatings on fracture footwalls and cavity floors in the welded tuffs at Yucca Mountain, the potential site of a high-level radioactive waste repository. These secondary mineral deposits are heterogeneously distributed in the unsaturated zone (UZ) with fewer than 10% of possible depositional sites mineralized. The paragenetic sequence, compiled from deposits throughout the UZ, consists of an early-stage assemblage of calcite??fluorite??zeolites that is frequently capped by chalcedony??quartz. Intermediate- and late-stage deposits consist largely of calcite, commonly with opal on buried growth layers or outermost crystal faces of the calcite. Coatings on steep-dipping fractures usually are thin (??? 3 mm) with low-relief outer surfaces whereas shallow-dipping fractures and lithophysal cavities typically contain thicker, more coarsely crystalline deposits characterized by unusual thin, tabular calcite blades up to several cms in length. These blades may be capped with knobby or corniced overgrowths of late-stage calcite intergrown with opal. The observed textures in the fracture and cavity deposits are consistent with deposition from films of water fingering down fracture footwalls or drawn up faces of growing crystals by surface tension and evaporated at the crystal tips. Fluid inclusion studies have shown that most early-stage and some intermediate-stage calcite formed at temperatures of 35 to 85??C. Calcite deposition during the past several million years appears to have been at temperatures < 30??C. The elevated temperatures indicated by the fluid inclusions are consistent with temperatures estimated from calcite ??18O values. Although others have interpreted the elevated temperatures as evidence of hydrothermal activity and flooding of the tuffs of the potential repository, the authors conclude that the temperatures and fluid-inclusion assemblages are consistent with deposition in a UZ environment that experienced prolonged heat input from gradual cooling of nearby plutons. The physical restriction of the deposits (and, therefore, fluid flow) to fracture footwalls and cavity floors and the heterogeneous and limited distribution of the deposits provides compelling evidence that they do not reflect flooding of the thick UZ at Yucca Mountain. The textures and isotopic and chemical compositions of these mineral deposits are consistent with deposition in a UZ setting from meteoric waters percolating downward along fracture flow paths.

A Sensor Based on LiCl/NaA Zeolite Composites for Effective Humidity Sensing.

PubMed

Zhang, Ying; Xiang, Hongyu; Sun, Liang; Xie, Qiuhong; Liu, Man; Chen, Yu; Ruan, Shengping

2018-03-01

LiCl/NaA zeolite composites were successfully prepared by doping 1 wt%, 2 wt%, 5 wt%, and 8 wt% of LiCl into NaA zeolite. The humidity sensing properties of LiCl/NaA composites were investigated among 11% 95% relative humidity (RH). The LiCl/NaA composites exhibited better humidity sensing properties than pure NaA zeolite. The sensor made by 2 wt% Li-doped NaA zeolite possesses the best linearly in the whole RH. These results demonstrate that the LiCl/NaA composites have the potential application in humidity sensing.

Increased thermal conductivity monolithic zeolite structures

DOEpatents

Klett, James; Klett, Lynn; Kaufman, Jonathan

2008-11-25

A monolith comprises a zeolite, a thermally conductive carbon, and a binder. The zeolite is included in the form of beads, pellets, powders and mixtures thereof. The thermally conductive carbon can be carbon nano-fibers, diamond or graphite which provide thermal conductivities in excess of about 100 W/mK to more than 1,000 W/mK. A method of preparing a zeolite monolith includes the steps of mixing a zeolite dispersion in an aqueous colloidal silica binder with a dispersion of carbon nano-fibers in water followed by dehydration and curing of the binder is given.

Molecular Monte Carlo Simulations Using Graphics Processing Units: To Waste Recycle or Not?

PubMed

Kim, Jihan; Rodgers, Jocelyn M; Athènes, Manuel; Smit, Berend

2011-10-11

In the waste recycling Monte Carlo (WRMC) algorithm, (1) multiple trial states may be simultaneously generated and utilized during Monte Carlo moves to improve the statistical accuracy of the simulations, suggesting that such an algorithm may be well posed for implementation in parallel on graphics processing units (GPUs). In this paper, we implement two waste recycling Monte Carlo algorithms in CUDA (Compute Unified Device Architecture) using uniformly distributed random trial states and trial states based on displacement random-walk steps, and we test the methods on a methane-zeolite MFI framework system to evaluate their utility. We discuss the specific implementation details of the waste recycling GPU algorithm and compare the methods to other parallel algorithms optimized for the framework system. We analyze the relationship between the statistical accuracy of our simulations and the CUDA block size to determine the efficient allocation of the GPU hardware resources. We make comparisons between the GPU and the serial CPU Monte Carlo implementations to assess speedup over conventional microprocessors. Finally, we apply our optimized GPU algorithms to the important problem of determining free energy landscapes, in this case for molecular motion through the zeolite LTA.

Petrology and trace element geochemistry of the Honolulu volcanics, Oahu: implications for the oceanic mantle below Hawaii.

USGS Publications Warehouse

Clague, D.A.; Frey, F.A.

1982-01-01

These volcanic rocks are the products of small-volume, late-stage vents along rifts cutting the older massive Koolan tholeiitic shield on Oahu. Most of the lavas and tuffs have the geochemical features expected of near-primary magmas derived from a peridotite source with olivine Fo87-89, e.g. 100 Mg/(Mg + Fe2+) > 65, Ni > 250 p.p.m. and the presence of ultramafic mantle xenoliths at 18 of the 37 vents. Thus the geochemistry of the alkali olivine basalt, basanite, nephelinite and nepheline melilitite lavas and tuffs of these Honolulu volcanic rocks has been used to deduce the composition of their mantle source and the conditions under which they were generated by partial melting in the mantle. New major- and trace-element analyses for 31 samples are tabulated and indicate derivation by partial melting of a garnet (<10%) lherzolite source which was isotopically homogeneous and compositionally uniform for most major and trace elements, though apparently heterogeneous in TiO2, Zr, Hf, Nb and Ta (due perhaps to the low inferred degrees of melting which failed to exhaust the source in minor residual phases). In comparison with estimates of a primordial mantle composition and the mantle source of MORB, the garnet peridotite source of these Honolulu volcanics was increasingly enriched in the sequence heavy REE, Y, Tb, Ti, Sm, Zr and Hf, for which a multi-stage history is required. This composition differs from the source of the previously erupted tholeiitic shield, nor is it represented in the upper-mantle xenoliths in the lavas and tuff of the unit.-R.A.H.

Synthesis and Characterization of Zeolite Na-Y and Its Conversion to the Solid Acid Zeolite H-Y

ERIC Educational Resources Information Center

Warner, Terence E.; Klokker, Mads Galsgaard; Nielsen, Ulla Gro

2017-01-01

Zeolite Y has an iconic crystal structure, but more importantly, the hydrogen modification zeolite H-Y is the classic example of a solid acid which is used extensively as a catalyst in the oil industry. This metastable compound cannot be synthesized directly, which creates an opportunity to discuss various preparative strategies with the students,…

An Ultrahigh CO2-Loaded Silicalite-1 Zeolite: Structural Stability and Physical Properties at High Pressures and Temperatures.

PubMed

Marqueño, Tomas; Santamaria-Perez, David; Ruiz-Fuertes, Javier; Chuliá-Jordán, Raquel; Jordá, Jose L; Rey, Fernando; McGuire, Chris; Kavner, Abby; MacLeod, Simon; Daisenberger, Dominik; Popescu, Catalin; Rodriguez-Hernandez, Placida; Muñoz, Alfonso

2018-06-04

We report the formation of an ultrahigh CO 2 -loaded pure-SiO 2 silicalite-1 structure at high pressure (0.7 GPa) from the interaction of empty zeolite and fluid CO 2 medium. The CO 2 -filled structure was characterized in situ by means of synchrotron powder X-ray diffraction. Rietveld refinements and Fourier recycling allowed the location of 16 guest carbon dioxide molecules per unit cell within the straight and sinusoidal channels of the porous framework to be analyzed. The complete filling of pores by CO 2 molecules favors structural stability under compression, avoiding pressure-induced amorphization below 20 GPa, and significantly reduces the compressibility of the system compared to that of the parental empty one. The structure of CO 2 -loaded silicalite-1 was also monitored at high pressures and temperatures, and its thermal expansivity was estimated.

Berriasian (Early Cretaceous) radiometric ages from the Grindstone Creek Section, Sacramento Valley, California

USGS Publications Warehouse

Bralower, T.J.; Ludwig, K. R.; Obradovich, J.D.

1990-01-01

The Grindstone Creek Section, Glenn County, Northern California is a sequence of hemipelagic mudstone, siltstone and sandstone interbedded with concretionary limestone and a few thin tuffs and bentonites. Two tuffs have been collected from a narrow interval of this sequence and subjected to mineralogical and isotopic analyses. UPb isotopic analyses of zircon fractions from these volcanic horizons indicate an age of 137.1 + 1.6/-0.6 Ma. A detailed investigation has been conducted on the calcareous nannofossil stratigraphy of this section based on numerous samples with moderately preserved assemblages. The nannoflora is largely of Tethyan affinity, and allows direct correlation with the Berriasian stratotype section, with sections with published magnetostratigraphies and with a DSDP site drilled between known magnetic anomalies. The dated tuffs lie in the lower part of the upper Berriasian Cretarhabdus angustiforatus Zone (Assipetra infracretacea Subzone) and within the narrow range of Rhagodiscus nebulosus. At three different sections, this subzone can be correlated with M-sequence Polarity Zones M16 and M16n. An independent magnetostratigraphic correlation is provided at DSDP Site 387, drilled between anomalies M15 and M16, where basal sediments contain R. nebulosus. Buchia collected within a meter of the lower tuff lie within the B. uncitoides Zone which is Berriasian in age. The upper tuff level, which occurs 65 m above the lower tuff, is situated within the overlying B. pacifica Zone. This zone had previously been correlated with the early Valanginian, but is clearly also partly of Berriasian age based on nannofossil stratigraphy. Our results allow an estimate of the age of the Berriasian-Valanginian and Jurassic-Cretaceous boundaries of 135.1 Ma and 141.1 Ma, respectively, and these fall within the range of, but differ significantiy from, several published time-scales. ?? 1990.

Assessment of the geothermal potential of southwestern New Mexico. Final report, July 1, 1978-April 30, 1980

DOE Office of Scientific and Technical Information (OSTI.GOV)

Elston, W.E.

1981-07-01

Results are reported of geologic mapping of geothermal anomalies in the Gila Hot Springs KGRA/Mimbres Hot Springs area, Grant County. They suggest that both hot-spring occurrences are structurally controlled by the intersection of a major Basin and Range fault and the disturbed margin of an ash-flow tuff cauldron. Hydrothermal alteration in both areas is related to mid-Tertiary volcanism, not to modern hot springs. At Gila Hot Springs, the geothermal aquifer is a zone at the contact between the unwelded top of a major ash-flow tuff sheet (Bloodgood Canyon Rhyolite Tuff) and a succession of interlayered vesicular basaltic andesite flows andmore » thin sandstone beds (Bearwallow Mountain Formation). Scattered groups of natural hot springs occur at intersections of this zone and the faults bordering the northeastern side of the Gila Hot Springs graben. Hydrothermal alteration of Bloodgood Canyon Rhyolite Tuff near major faults seems to have increased its permeability. At Mimbres Hot Springs, a single group of hot springs is controlled by the intersection of the Mimbres Hot Springs fault and a fractured welded ash-flow tuff that fills the Emory cauldron (Kneeling Nun Tuff). Gila Hot Springs and Mimbres Hot Springs do not seem to be connected by throughgoing faults. At both localities, hot spring water is used locally for space heating and domestic hot water; at Gila Hot Springs, water of 65.6/sup 0/C (150/sup 0/F) is used to generate electricity by means of a 10 kw freon Rankine Cycle engine. This is the first such application in New Mexico.« less

Geochronology and Regional Correlation of Continental Permo-Triassic Sediments in West Texas

NASA Astrophysics Data System (ADS)

Mitchell, W.; Renne, P. R.; Mundil, R.; Chang, S.; Geissman, J. W.; Tabor, N. J.; Mack, G.

2011-12-01

Although many aspects of marine sections spanning the Permian-Triassic boundary (PTB) have been studied in great detail across a broad paleogeographic area, less is known about the timing, pace, and extent of environmental changes and extinctions across this boundary in continental environments, particularly along the Panthalassa margin. Extensive outcrops in the Ochoan Series of west Texas provide an opportunity to investigate the terrestrial record spanning the PTB. The presence of several silicic tuffs in these sections allows for precise radioisotopic dating using both U-Pb and 40Ar/39Ar techniques. Dated strata then serve as a calibration basis for paleomagnetic and lithostratigraphic studies and facilitate stratigraphic correlation across the few to hundreds of kilometers separating study sites. Depending on the possible correlations, as many as seven tuffs have been identified in this region, the ages of which are within about a million years of the chronometrically-defined PTB at the Meishan section in China at ca. 252 Ma. Data obtained thus far indicate that the PTB occurs within the Quartermaster/Dewey Lake Formation. With the aims of determining the number and ages of distinct tuffs found and facilitating a well-correlated regional stratigraphy among the studied sections, we present preliminary radioisotopic age determinations of, and correlations among, these tuffs using the zircon U-Pb system, 40Ar/39Ar dating where possible, as well as mineral chemistry. Our results include the first dated tuff in the Ochoan Series that lies within the Alibates Formation which underlies the Dewey Lake Fm. Other samples in progress from the various tuffs in the region, in combination with results from magneto- and chemostratigraphy, will significantly expand the areal coverage of these strata and lead towards a greatly improved chronostratigraphic framework.

Volcano-stratigraphy and 40Ar/ 39Ar geochronology of the Macusani ignimbrite field: monitor of the Miocene geodynamic evolution of the Andes of southeast Peru

NASA Astrophysics Data System (ADS)

Cheilletz, Alain; Clark, Alan H.; Farrar, Edward; Pauca, Guido Arroyo; Pichavant, Michel; Sandeman, Hamish A.

1992-04-01

A total of 1400 m of ignimbritic ash-flow tuffs distributed in five cross-sections and extending from the pre-Neogene base to the uppermost flows were studied in the Miocene Macusani ignimbrite basin (southeast Peru). Volcano-stratigraphic interpolation and precise 40Ar/ 39Ar dating of sanidine, biotite, and rhyolitic glass from the ash-flow tuffs give rise to a southwest-northeast correlation chart subdivided into six volcanic cycles or fundamental cooling units i.e., (1) 10.0 ± 0.5; (2) 7.8-8.0 ± 0.1; (3) 7.5 ± 0.1; (4) 7.3 ± 0.1; (5) 6.8-7.0 ± O.1; and (6) 6.7 ± O.1 Ma. These delimit two brief e 10 ± 1 and 7 ± 1 Ma, which are sensibly synchronous with the Quechua 2 and Quechua 3 compressional events characterizing the tectonic regime in the Central Andes. This close relationship between tectonic pulses and felsic magmatic activity adds a supplementary constraint to models of the Miocene tectono-magmatic evolution of the Cordillera Oriental. The stratigraphic relationships of the uranium mineralization of the Macusani field are defined for the first time: the stratiform-stratabound occurrences are restricted to three main cooling units dated at 7.8, 7.5 and 6.9-6.8 Ma which constitute a maximum age for uranium deposition.

Characterization of Water and CO2 Adsorption by Stores 3A Desiccant Samples Using Thermal Gravimetric Analysis and Fourier Transform Infrared Spectroscopy

DOE Office of Scientific and Technical Information (OSTI.GOV)

RIVERA, DION A.; ALAM, M. KATHLEEN; MARTIN, LAURA

2003-02-01

Two lots of manufactured Type 3a zeolite samples were compared by TGA/IR analysis. The first lot, obtained from Davidson Chemical, a commercial vendor, was characterized during the previous study cycle for its water and water-plus-CO{sub 2} uptake in order to determine whether CO{sub 2} uptake prevented water adsorption by the zeolite. It was determined that CO{sub 2} did not hamper water adsorption using the Davidson zeolite. CO{sub 2} was found on the zeolite surface at dewpoints below -40 C, however it was found to be reversibly adsorbed. During the course of the previous studies, chemical analyses revealed that the Davidsonmore » 3a zeolite contained calcium in significant quantities, along with the traditional counterions potassium and sodium. Chemical analysis of a Type 3a zeolite sample retrieved from Kansas City (heretofore referred to as the ''Stores 3a'' sample) indicated that the Stores sample was a more traditional Type 3a zeolite, containing no calcium. TGA/IR studies this year focused on obtaining CO{sub 2} and water absorbance data from the Stores 3a zeolite. Within the Stores 3a sample, CO{sub 2} was found to be reversibly absorbed within the sample, but only at and below -60 C with 5% CO{sub 2} loading. The amount of CO{sub 2} observed eluting from the Stores zeolite at this condition was similar to what was observed from the Davidson zeolite sample but with a greater uncertainty in the measured value. The results of the Stores 3a studies are summarized within this report.« less

Nano-sized zeolites as modulators of thiacloprid toxicity on Chironomus riparius

PubMed Central

Wicht, Anna-Jorina; Guluzada, Leyla; Crone, Barbara; Karst, Uwe; Lee, Hwa Jun; Triebskorn, Rita; Haderlein, Stefan B.; Huhn, Carolin; Köhler, Heinz-R.

2017-01-01

This study investigated whether zeolites of different size (Y30 (nano-sized) and H-Beta(OH)-III (forming large aggregates/agglomerates composed of 50 nm small primary particles)) exerted acute toxicity on larvae of the non-biting midge, Chironomus riparius, and whether such zeolites are able to modulate the toxicity of a common insecticide, thiacloprid, by means of adsorption of a dissolved toxicant. We conducted acute toxicity tests with fourth instar larvae of C. riparius. In these tests, larvae were exposed to zeolites or thiacloprid solely, or to mixtures of both compounds. The mixtures comprised 1.0 µg/L thiacloprid in addition to low (5.2 mg/L), medium (18.2 mg/L), and high (391.7 mg/L) zeolite concentrations, resulting in different adsorption rates of thiacloprid. As biological endpoints, changes in mortality rates and in behavior were monitored every 24 h over a total investigation period of 96 h. Furthermore, we conducted chemical analyses of thiacloprid in the medium and the larvae and located the zeolite particles within the larvae by LA-ICP-MS imaging techniques. Our results demonstrate that both types of zeolites did not exert acute toxicity when applied as single-substances, but led to reduced acute toxicity of thiacloprid when applied together with thiacloprid. These results are in line with the sorption properties of zeolites indicating reduced bioavailability of thiacloprid, although our data indicate that thiacloprid can desorb from zeolites to some extent. While freely dissolved (i.e., non-sorbed) fraction of thiacloprid was a good parameter to roughly estimate toxic effects, it did not correlate with measured internal thiacloprid concentrations. Moreover, it was shown that both zeolite types were ingested by the larvae, but no indication for cellular uptake of them was found. PMID:28729952

Preliminary appraisal of gravity and magnetic data of Syncline Ridge, western Yucca Flat, Nevada Test Site, Nye County, Nevada

USGS Publications Warehouse

Ponce, David A.; Hanna, William F.

1982-01-01

A gravity and magnetic study of the Syncline Ridge area was conducted as part of an investigation of argillite rocks of the Eleana Formation under consideration as a medium for the possible storage of high-level radioactive waste. Bouguer gravity anomaly data, viewed in light of densities obtained by gamma-gamma logs and previous work of D. L. Healey (1968), delineate two regions of steep negative gradient where Cenozoic rocks and sediments are inferred to abruptly thicken: (1) the western third of the study area where Tertiary volcanic rocks are extensively exposed and (2) the northeast corner of the area where Quaternary alluvium is exposed and where volcanic rocks are inferred to occur at depth. In the remainder of the area, a region extending contiguously from Mine Mountain northwestward through Syncline Ridge to the Eleana Range, the gravity data indicate that the Eleana Formation, where not exposed, is buried at depths of less than about 200 m, except in a limited area of exposed older Paleozoic rocks on Mine Mountain. Quaternary alluvium and Tertiary volcanic rocks are inferred to occur in this region as veneers or shallow dishes of deposit on Tippipah Limestone or Eleana Formation. Low-level aeromagnetic anomaly data, covering the western two-thirds of the study area, delineate relatively magnetic tuff units within the Tertiary volcanic rocks and provide a very attractive means for distinguishing units of normal polarization from units of reversed polarization. If used in conjunction with results of previous magnetization studies of G. D. Bath (1968), the low-level survey may prove to be an effective tool for mapping specific tuff members in the volcanic terrane. The important question of the feasibility of discriminating high-quartz argillite from low-quartz argillite of the Eleana Formation using surface gravity data remains unresolved. If the more highly competent, denser, high-quartz phase should occur as stratigraphic units many tens of meters thick, closely spaced gravity data may reliably detect these units. If the high-quartz phase occurs only as relatively thin units, interbedded with low-quartz phase, borehole gravity surveying can be used much more effectively than equivalent surface gravity surveying.

Preparation of a Versatile Bifunctional Zeolite for Targeted Imaging Applications

PubMed Central

Ndiege, Nicholas; Raidoo, Renugan; Schultz, Michael K.; Larsen, Sarah

2011-01-01

Bifunctional zeolite Y was prepared for use in targeted in vivo molecular imaging applications. The strategy involved functionalization of the external surface of zeolite Y with chloropropyltriethoxysilane followed by reaction with sodium azide to form azide-functionalized NaY, which is amenable to copper(1) catalyzed click chemistry. In this study, a model alkyne (4-pentyn-1-ol) was attached to the azide-terminated surface via click chemistry to demonstrate feasibility for attachment of molecular targeting vectors (e.g., peptides, aptamers) to the zeolite surface. The modified particle efficiently incorporates the imaging radioisotope gallium-68 (68Ga) into the pores of the azide-functionalized NaY zeolite to form a stable bifunctional molecular targeting vector. The result is a versatile “clickable” zeolite platform that can be tailored for future in vivo molecular targeting and imaging modalities. PMID:21306141

Molecular simulation of water removal from simple gases with zeolite NaA.

PubMed

Csányi, Eva; Ható, Zoltán; Kristóf, Tamás

2012-06-01

Water vapor removal from some simple gases using zeolite NaA was studied by molecular simulation. The equilibrium adsorption properties of H(2)O, CO, H(2), CH(4) and their mixtures in dehydrated zeolite NaA were computed by grand canonical Monte Carlo simulations. The simulations employed Lennard-Jones + Coulomb type effective pair potential models, which are suitable for the reproduction of thermodynamic properties of pure substances. Based on the comparison of the simulation results with experimental data for single-component adsorption at different temperatures and pressures, a modified interaction potential model for the zeolite is proposed. In the adsorption simulations with mixtures presented here, zeolite exhibits extremely high selectivity of water to the investigated weakly polar/non-polar gases demonstrating the excellent dehydration ability of zeolite NaA in engineering applications.

Changing of Sumatra backswamp peat properties by seawater and zeolite application

NASA Astrophysics Data System (ADS)

Sarifuddin; Nasution, Z.; Rauf, A.; Mulyanto, B.

2018-02-01

This research attempts to improve the properties of backswamp peatsoil originated from Asahan District, North Sumatra Indonesia by adding sea water and zeolite using factorial randomized block design with volume of sea water as first factor, consisting of without seawater, 500 ml, 1000 ml and 1500 ml and second factor are dosages of zeolite consisting of without zeolite, 100 g, 200 g each 10 kgs of wet peat soil. at green house in faculty of agriculture University of Sumatra Utara (USU) Medan, Indonesia. The result showed that the application of seawater decreased pH, C/N and Cation Exchange Capacity and increased of base saturation of peat soil. Adding of zeolite minerals can buffered the increasing of acidity and Electric Conductivity caused by sea water application. Interaction seawater + zeolite decreased of C/N and increased of percent of base saturation.

Application of nuclear magnetic resonance spectroscopy, Fourier transform infrared spectroscopy, UV-Visible spectroscopy and kinetic modeling for elucidation of adsorption chemistry in uptake of tetracycline by zeolite beta.

PubMed

Kang, Jin; Liu, Huijuan; Zheng, Yu-Ming; Qu, Jiuhui; Chen, J Paul

2011-02-01

Extensive usage of tetracycline has resulted in its contamination in surface water and groundwater. The adsorption of tetracycline on zeolite beta was systematically investigated for the decontamination of the antibiotic polluted water in this study. Ninety percent of uptake by the zeolite beta occured in 0.25h, and the adsorption equilibrium was obtained within 3h, which was well described by an intraparticle diffusion model. The adsorption generally increased when pH was increased from 4.0 to 5.0, and then decreased significantly as the pH was further increased, which was caused by the pH-dependent speciation of tetracycline and surface charge of zeolite beta. Both Freundlich and Langmuir equations well described the adsorption isotherm. A thermodynamic analysis showed that the sorption process was spontaneous and endothermic. Aluminum atoms in the zeolite played a crucial role in the uptake; the adsorption increased with the increasing aluminum content in zeolite. The UV-Visible spectroscopy study showed that the spectra of tetracycline changed upon the interaction with zeolite beta, which could be ascribed to the formation of complexes of tetracycline and aluminum atoms in the zeolite surface. Nuclear magnetic resonance spectroscopy study further confirmed the participation of Al in the tetracycline adsorption. Fourier transform infrared spectroscopy studies showed that the amino functional groups in tetracycline were involved in the complexation with the zeolite surface. Copyright © 2010 Elsevier Inc. All rights reserved.

Characterization of Zeolite in Zeolite-Geopolymer Hybrid Bulk Materials Derived from Kaolinitic Clays

PubMed Central

Takeda, Hayami; Hashimoto, Shinobu; Yokoyama, Hiroaki; Honda, Sawao; Iwamoto, Yuji

2013-01-01

Zeolite-geopolymer hybrid materials have been formed when kaolin was used as a starting material. Their characteristics are of interest because they can have a wide pore size distribution with micro- and meso-pores due to the zeolite and geopolymer, respectively. In this study, Zeolite-geopolymer hybrid bulk materials were fabricated using four kinds of kaolinitic clays (a halloysite and three kinds of kaolinite). The kaolinitic clays were first calcined at 700 °C for 3 h to transform into the amorphous aluminosilicate phases. Alkali-activation treatment of the metakaolin yielded bulk materials with different amounts and types of zeolite and different compressive strength. This study investigated the effects of the initial kaolinitic clays on the amount and types of zeolite in the resultant geopolymers as well as the strength of the bulk materials. The kaolinitic clays and their metakaolin were characterized by XRD analysis, chemical composition, crystallite size, 29Si and 27Al MAS NMR analysis, and specific surface area measurements. The correlation between the amount of zeolite formed and the compressive strength of the resultant hybrid bulk materials, previously reported by other researchers was not positively observed. In the studied systems, the effects of Si/Al and crystalline size were observed. When the atomic ratio of Si/Al in the starting kaolinitic clays increased, the compressive strength of the hybrid bulk materials increased. The crystallite size of the zeolite in the hybrid bulk materials increased with decreasing compressive strength of the hybrid bulk materials. PMID:28809241

Synthetic Zeolites as Controlled-Release Delivery Systems for Anti-Inflammatory Drugs.

PubMed

Khodaverdi, Elham; Soleimani, Hossein Ali; Mohammadpour, Fatemeh; Hadizadeh, Farzin

2016-06-01

Scientists have always been trying to use artificial zeolites to make modified-release drug delivery systems in the gastrointestinal tract. An ideal carrier should have the capability to release the drug in the intestine, which is the main area of absorption. Zeolites are mineral aluminosilicate compounds with regular structure and huge porosity, which are available in natural and artificial forms. In this study, soaking, filtration and solvent evaporation methods were used to load the drugs after activation of the zeolites. Weight measurement, spectroscopy FTIR, thermogravimetry and scanning electronic microscope were used to determine drug loading on the systems. Finally, consideration of drug release was made in a simulated gastric fluid and a simulated intestinal fluid for all matrixes (zeolites containing drugs) and drugs without zeolites. Diclofenac sodium (D) and piroxicam (P) were used as the drug models, and zeolites X and Y as the carriers. Drug loading percentage showed that over 90% of drugs were loaded on zeolites. Dissolution tests in stomach pH environment showed that the control samples (drug without zeolite) released considerable amount of drugs (about 90%) within first 15 min when it was about 10-20% for the matrixes. These results are favorable as NSAIDs irritate the stomach wall and it is ideal not to release much drugs in the stomach. Furthermore, release rate of drugs from matrixes has shown slower rate in comparison with control samples in intestine pH environment. © 2016 John Wiley & Sons A/S.