Environmental Assessment of Selected Cone Penetrometer Grouts and a Tracer
1993-08-01
Bentonite Clay ............ ...................... A2 Attapulgite Clay ................................... A22 Microfine Portland Cement...and the tracer are a. Bentonite clay. b. Attapulgite clay. c. Microfine portland cement. d. Joosten grout (calcium silicate grout). e. Urethane grout. f...Inc., on an attapulgite clay product (trade name: Zeogel). " Microfine portland cement. Information was obtained for two micro- fine portland cements
Modification of hydraulic conductivity in granular soils using waste materials.
Akbulut, S; Saglamer, A
2004-01-01
This paper evaluates the use of waste products such as silica fume and fly ash in modification of the granular soils in order to remove some environmental problems and create new useful findings in the field of engineering. It is known that silica fume and fly ash, as well as clay material, are used in geotechnical engineering because of their pozzolanic reactivity and fineness to improve the soil properties needed with respect to engineering purposes. The main objective of this research project was to investigate the use of these materials in geotechnical engineering and to improve the hydraulic properties of soils by means of grouting. For this reason, firstly, suitable grouts in suspension forms were prepared by using silica fume, fly ash, clay and cement in different percentages. The properties of these cement-based grouts were then determined to obtain the desired optimum values for grouting. After that, these grouts were penetrated into the soil samples under pressure. The experimental work indicates that these waste materials and clay improved the physical properties and the fluidity of the cement-based grouts and they also decreased the hydraulic conductivity of the grouted soil samples by sealing the voids of the soil. The results of this study have important findings concerning the use of these materials in soil treatment and the improvement of hydraulic conductivity of the soils.
Studies on thermal reactions and sintering behaviour of red clays by irreversible dilatometry
NASA Astrophysics Data System (ADS)
Anil, Asha; Misra, S. N.; Misra, N. M.
2018-05-01
Thermal behavior of clays strongly influences that of ceramic bodies made thereof and hence, its study is must for assessing its utility in ceramic products as well as to set the body composition. Irreversible dilatometry is an effective thermal analysis tool for evaluating thermal reactions as well as sintering behavior of clays or clay based ceramic bodies. In this study, irreversible dilatometry of four red clay samples (S, M, R and G) of Gujarat region, which vary in their chemical and mineralogical compositions was carried out using a Dilatometer and compared. Chemical analysis and XRD of red clays were carried out. XRD showed that major clay minerals in S, M and R clays are kaolinite. However, clay marked R and G showed presence of both kaolinite and illite and /muscovite. Presence of non-clay minerals such as hematite, quartz, anatase were also observed in all clays. XRD results were in agreement with chemical analyses results. Rational analyses showed variation in amount of clay and non-clay minerals in red clay samples. Evaluation of dilatometric curves showed that clay marked as S, M and R exhibit patterns typical for kaolinitic clays. Variation in linear expansion (up to 550°C) and shrinkage (above 550°C) between these three clays was found to be related to difference in amount of quartz and kaolinite respectively. However, dilatometric curve of G exhibit a pattern similar to that for an illitic clay. This study confirmed that sintering of investigated kaolinitic and illitic and / muscovitic red clays initiates at above 1060°C and 860°C respectively and this behaviour strongly depends upon type and amount of minerals and their chemical compositions.
NASA Astrophysics Data System (ADS)
Ginil Mon, S.; Jaya Vinse Ruban, Y.; Vetha Roy, D.
2011-09-01
In the large field of nanotechnology, polymer matrix-based nanocomposites have become a prominent area of current research and development. Exfoliated clay-based nanocomposites have dominated the polymer world with excellent characteristics. EPDM rubber composites have been synthesized by solution-intercalation using the easily available kaolinite as filler. The composite structure has been elucidated by X-ray diffraction (XRD), Fourier transform IR, and scanning electron microscope studies. The molecular level dispersion of clay layers has been verified by the disappearance of basal XRD peak of kaolinite in the EPDM/kaolinite composites. The mechanical properties showed significant improvement of EPDM/kaolinite composites with respect to neat EPDM.
Clay-cement suspensions - rheological and functional properties
NASA Astrophysics Data System (ADS)
Wojcik, L.; Izak, P.; Mastalska-Poplawska, J.; Gajek, M.
2017-01-01
The piping erosion in soil is highly unexpected in civil engineering. Elimination of such damages is difficult, expensive and time-consuming. One of the possibility is the grouting method. This method is still developed into direction of process automation as well as other useful properties of suspensions. Main way of modernization of the grouting method is connected it with rheology of injection and eventuality of fitting them to specific problems conditions. Very popular and useful became binders based on modified clays (clay-cement suspensions). Important principle of efficiency of the grouting method is using of time-dependent pseudothixotropic properties of the clay-cement suspensions. The pseudo-rheounstability aspect of the suspensions properties should be dedicated and fitted to dynamic changes of soil conditions destructions. Whole process of the modification of the suspension rheology is stimulated by the specific agents. This article contains a description of practical aspects of the rheological parameters managing of the clay-cement suspensions, dedicated to the building damages, hydrotechnic constructions etc.
Improved method and composition for immobilization of waste in cement-based material
Tallent, O.K.; Dodson, K.E.; McDaniel, E.W.
1987-10-01
A composition and method for fixation or immobilization of aqueous hazardous waste material in cement-based materials (grout) is disclosed. The amount of drainable water in the cured grout is reduced by the addition of an ionic aluminum compound to either the waste material or the mixture of waste material and dry-solid cement- based material. This reduction in drainable water in the cured grout obviates the need for large, expensive amounts of gelling clays in grout materials and also results in improved consistency and properties of these cement-based waste disposal materials.
Cai, Li; Tong, Meiping; Wang, Xueting; Kim, Hyunjung
2014-07-01
This study investigated the influence of two representative suspended clay particles, bentonite and kaolinite, on the transport of titanium dioxide nanoparticles (nTiO2) in saturated quartz sand in both NaCl (1 and 10 mM ionic strength) and CaCl2 solutions (0.1 and 1 mM ionic strength) at pH 7. The breakthrough curves of nTiO2 with bentonite or kaolinite were higher than those without the presence of clay particles in NaCl solutions, indicating that both types of clay particles increased nTiO2 transport in NaCl solutions. Moreover, the enhancement of nTiO2 transport was more significant when bentonite was present in nTiO2 suspensions relative to kaolinite. Similar to NaCl solutions, in CaCl2 solutions, the breakthrough curves of nTiO2 with bentonite were also higher than those without clay particles, while the breakthrough curves of nTiO2 with kaolinite were lower than those without clay particles. Clearly, in CaCl2 solutions, the presence of bentonite in suspensions increased nTiO2 transport, whereas, kaolinite decreased nTiO2 transport in quartz sand. The attachment of nTiO2 onto clay particles (both bentonite and kaolinite) were observed under all experimental conditions. The increased transport of nTiO2 in most experimental conditions (except for kaolinite in CaCl2 solutions) was attributed mainly to the clay-facilitated nTiO2 transport. The straining of larger nTiO2-kaolinite clusters yet contributed to the decreased transport (enhanced retention) of nTiO2 in divalent CaCl2 solutions when kaolinite particles were copresent in suspensions.
Hosterman, John W.; Loferski, Patricia J.
1978-01-01
The distribution of kaolinite in parts of the Devonian shale section is the most significant finding of this work. These shales are composed predominately of 2M illite and illitic mixed-layer clay with minor amounts of chlorite and kaolinite. Preliminary data indicate that kaolinite, the only allogenic clay mineral, is present in successively older beds of the Ohio Shale from south to north in the southern and middle parts of the Appalachian basin. This trend in the distribution of kaolinite shows a paleocurrent direction to the southwest. Three well-known methods of preparing the clay fraction for X-ray diffraction analysis were tested and evaluated. Kaolinite was not identified in two of the methods because of layering due to differing settling rates of the clay minerals. It is suggested that if one of the two settling methods of sample preparation is used, the clay film be thin enough for the X-ray beam to penetrate the entire thickness of clay.
Origin, distribution, and rapid removal of hydrothermally formed clay at Mount Baker, Washington
Frank, David
1983-01-01
Clay minerals are locally abundant in two hydrothermal areas at Mount Baker-Sherman Crater and the Dorr Fumarole Field. The silt- and clay-size fractions of volcanic debris that is undergoing alteration at and near the ground surface around areas of current fumarolic activity in Sherman Crater are largely dominated by alunite and a silica phase, either opal or cristobalite, but contain some kaolinite and smectite. Correspondingly, the chemistry of solutions at the surface of the crater, as represented by the crater lake, favors the formation of alunite over kaolinite. In contrast, vent-filling debris that was ejected to the surface from fumaroles in 1975 contains more than 20 percent clay-size material in which kaolinite and smectite are dominant. The youngest eruptive deposit (probably 19th century) on the crater rim was also altered prior to ejection and contains as much as 27 percent clay-size material in which kaolinite, smectite, pyrophyllite, and mixed-layer illitesmectite are abundant. The hydrothermal products, kaolinite and alunite, are present in significant amounts in five large Holocene mudflows that originated at the upper cone of Mount Baker. The distribution of kaolinite in crater and valley deposits indicates that, with the passage of time, increasingly greater amounts of this clay mineral have been incorporated into large mass movements from the upper cone. Either erosion has cut into more kaolinitic parts of the core of Sherman Crater, or the amount of kaolinite has increased through time in Sherman Crater.
NASA Astrophysics Data System (ADS)
Ben M'barek-Jemaï, Moufida; Sdiri, Ali; Ben Salah, Imed; Ben Aissa, Lassaad; Bouaziz, Samir; Duplay, Joelle
2017-05-01
Late Jurassic-Lower Cretaceous clays of the Jebel Ammar study site were used as raw materials for potential applications in ceramic industry. Physico-chemical characterization of the collected samples was performed using atomic absorption spectroscopy, X-ray diffraction, thermogravimetry and dilatometry (Bugot's curve). Geotechnical study was also undertaken by the assessment of plasticity and liquidity limits. It was found that high concentrations of silica, alumina with SiO2/Al2O3 ratio characterized the studied clays; its high amounts of CaO and Fe2O3 in the Late Jurassic clays indicated their calcareous nature. In addition, technological tests indicated moderate to low plasticity values for the Late Jurassic and Lower Cretaceous clays, respectively. Clay fraction (<2 μm) reached 50% of the natural clay in some cases. Mineralogical analysis showed that Jurassic clays were dominated by smectite, illite and kaolinite, as clay mineral species; calcite was the main associated mineral. Lower Cretaceous clays were mainly composed of abundant illite accompanied by well-crystallized smectite and kaolinite. Kaolinite gradually increased upwards, reaching 70% of the total clay fraction (i.e. <2 μm). Quartz, calcite and feldspar were the main non-clay minerals. Based on these analyses, the clays meet technological requirements that would allow their use in the ceramic industry and for the manufacturing of ceramic tiles.
Organic Pollutants in Soils, as Studied by Nuclear Magnetic Resonance
1998-05-15
represented in most of this study by the ’ following major soil components: humics (humic acid, fulvic acid, humin), clays ( montmorillonite , kaolinite ...fulvic acids and clays ( kaolinite and montmorillonite ). This study was designed to provide the kind of fundamental chemical/physical information...elemental analysis and 29Si and 27A1 NMR data, are a kaolinite and a Ca- montmorillonite obtained from the Missouri Clay Repository, Columbia, MO. Figures
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
2004-09-01
report increasing adsorption capacity depending on the specific clay type, in the order kaolinite < illite < montmorillonite (11). This finding suggests... kaolinite , illite, and montmorillonite . Finally, there is a wide varia- tion in adsorption constants among the different nitroaromatic compounds...common to micas, chlorites, pyrophyllite, talc, kaolinite , and gibbsite . As is now known, clays typically consist of layered crystalline structures
The clays of the United States east of the Mississippi River
Ries, Henrich
1903-01-01
Since clays vary mineralogically they vary also chemically, but the plasticity may remain the same through a wide range of chemical composition, and this property is evidently not dependent on the chemical composition alone, but is due rather to some physical cause. The plasticity may be destroyed by heating the clay to a sufficiently high temperature to drive off the chemically combined water. Although varying in their mineral composition, most clays are supposed to contain more or less of the mineral kaolinite (a hydrated silicate of alumina), which is commonly referred to as the clay base or clay substance. The adoption of the latter term has probably arisen from the fact that many have 'considered this mineral to be the cause of plasticity, an idea now known to be somewhat incorrect, because some of the most plastic clays contain but small quantities of kaolinite, and vice versa.
1989-10-01
montmorillonite enhanced the growth of smooth brome grass. Topsoil, the clays attapulgite and kaolinite , and the commercial products Agrosoke anj Stawetwere...clays bentonite, attapulgite, kaolinite , and montmorillonite . Trade name and company addresses for the clays are listed in Table 1. Agrosoke and Stawet...desertcoZa, G. etunicatwn, and G. intraradice8. The clays attapulgite, ben- tonite, kaclinite,/and montmorillonite from various commercial sources were
Zeta Potential Measurements on Three Clays from Turkey and Effects of Clays on Coal Flotation
Hussain; Dem&idot;rc&idot;; özbayoğlu
1996-12-25
There is a growing trend of characterizing coal and coal wastes in order to study the effect of clays present in them during coal washing. Coarse wastes from the Zonguldak Coal Washery, Turkey, were characterized and found to contain kaolinite, illite, and chlorite. These three clays, obtained in almost pure form from various locations in Turkey, have been subjected to X-ray diffraction (XRD) analysis to assess their purity and zeta potential measurements in order to evaluate their properties in terms of their surface charge and point of zero charge (pzc) values. It was found from XRD data that these clays were almost pure and their electrokinetic potential should therefore be representative of their colloidal behavior. All three clay minerals were negatively charged over the range from pH 2.5 to 11. Chlorite and illite have pzc at pH 3 and pH 2.5, respectively, whereas kaolinite has no pzc. The effect of these clays in Zonguldak coal, wastes, and black waters on coal flotation was studied by floating artificial mixtures of Zonguldak clean coal (4.5% ash) and individual clay. The flotation tests on coal/individual clay revealed that each clay influences coal flotation differently according to its type and amount. Illite had the worst effect on coal floated, followed by chlorite and kaolinite. The loss of yield in coal was found to be 18% for kaolinite, 20% for chlorite, and 28% for illite, indicating the worst effect of illite and least for kaolinite during coal flotation.
Clay mineralogy of weathering profiles from the Carolina Piedmont.
Loferski, P.J.
1981-01-01
Saprolite profiles (12) that formed over various crystalline rocks from the Charlotte 1o X 2o quadrangle showed overall similarity in their clay mineralogy to depths of 6 to 45 m indicating control by weathering processes rather than by rock type. Most saprolite contained 10-25% clay, and ranged 3 to 70%. Kaolinite and halloysite composed = or >75% of the clay fraction of most samples. The ratio kaolinite:halloysite ranged widely, from 95% kaolinite to 90% halloysite, independent of depth. Clay-size mica was present in all profiles, and ranged 5-75% over a sericite schist. Mixed-layer mica-smectite and mica-vermiculite were subordinate; discrete smectite and vermiculite were rare. The abundance of halloysite indicates a continuously humid environment since the time of profile formation, because of the rapidity with which halloysite dehydrates irreversibly. -R.S.M.
Near-infrared reflectance spectra of mixtures of kaolin-group minerals: Use in clay mineral studies
Crowley, James K.; Vergo, Norma
1988-01-01
Near-infrared (NIR) reflectance spectra for mixtures of ordered kaolinite and ordered dickite have been found to simulate the spectral response of disordered kaolinite. The amount of octahedral vacancy disorder in nine disordered kaolinite samples was estimated by comparing the sample spectra to the spectra of reference mixtures. The resulting estimates are consistent with previously published estimates of vacancy disorder for similar kaolin minerals that were modeled from calculated X-ray diffraction patterns. The ordered kaolinite and dickite samples used in the reference mixtures were carefully selected to avoid undesirable particle size effects that could bias the spectral results.NIR spectra were also recorded for laboratory mixtures of ordered kaolinite and halloysite to assess whether the spectra could be potentially useful for determining mineral proportions in natural physical mixtures of these two clays. Although the kaolinite-halloysite proportions could only be roughly estimated from the mixture spectra, the halloysite component was evident even when halloysite was present in only minor amounts. A similar approach using NIR spectra for laboratory mixtures may have applications in other studies of natural clay mixtures.
The Influence of Soil Suction on the Shear Strength of Unsaturated Soil
1990-09-01
the shear strength parameters c’ and 0’ for montmorillonitic and kaolinitic clays increased following the addition of divalent calcium hydroxide to...503-513. Sridharan, A., Rao, S.N., and Rao, G.V. (1971), "Shear Strength Char- acteristics of Saturated Montmorillonite and Kaolinite Clays," Soils...Summary of Shear Strengths of Unsaturated Specimens of Compacted Kaolinite and Compacted Red Earth (After Murthy, Sridharan and Nagaraj, 1987
Zhang, Ling; Lu, Qingye; Xu, Zhenghe; Liu, Qingxia; Zeng, Hongbo
2012-07-15
The interactions between kaolinite clay particles and a comb-type polymer (polycarboxylate ether or PCE), so-called PCE super-plasticizer, were investigated through viscosity and surface forces measurements by a rheometer and a Surface Forces Apparatus (SFA). The addition of PCE shows a strong impact on the viscosity of concentrated kaolinite suspensions in alkaline solutions (pH=8.3) but a weak effect under acidic conditions (pH=3.4). In acidic solutions, the high viscosity measured is attributed to the strong electrostatic interaction between negatively charged basal planes and positively charged edge surfaces of clay particles. Under the alkaline condition, the suspension viscosity was found to first increase significantly and then decrease with increasing PCE dosages. The results from surface forces measurement show that PCE molecules at low dosages can bridge the kaolinite particles in the concentrated suspensions via hydrogen bonding, leading to the formation of a kaolinite-PCE "network" and hence an increased suspension viscosity. At high PCE dosages, clay particles are fully covered by PCE molecules, leading to a more dispersed kaolinite suspensions and hence lower suspension viscosity due to steric repulsion between the adsorbed PCE molecules. The insights derived from measuring viscosity and interfacial properties of kaolinite suspensions containing varying amount of comb-type super-plasticizer PCE at different pH provide the foundation for many engineering applications and optimizing industrial processes. Copyright © 2012 Elsevier Inc. All rights reserved.
Clay alteration and gold deposition in the genesis and blue star deposits, Eureka County, Nevada
Drews-Armitage, S. P.; Romberger, S.B.; Whitney, C.G.
1996-01-01
The Genesis and Blue Star sedimentary rock-hosted gold deposits occur within the 40-mile-long Carlin trend and are located in Eureka County, Nevada. The deposits are hosted within the Devonian calcareous Popovich Formation, the siliciclastic Rodeo Creek unit and the siliciclastic Vinini Formation. The host rocks have undergone contact metamorphism, decalcification, silicification, argillization, and supergene oxidation. Detailed characterization of the alteration patterns, mineralogy, modes of occurrence, and associated geochemistry of clay minerals resulted in the following classifications: least altered rocks, found distal to the orebody, consisting of both metamorphosed and unmetamorphosed host rock that has not been completely decalcified; and altered rocks, found proximal to the orebody that have been decalcified. Altered rocks are classified further into the following groups based on clay mineral content: silicic, 1 to 10 percent clay; silicicargillic, 10 to 35 percent clay; and argillic, 35 to 80 percent clay. Clay species identified are 1M illite, 2M1 illite, kaolinite, halloysite, and dioctahedral smectite. An early hydrothermal event resulted in the precipitation of euhedral kaolinite and at least one generation of silica. This event occurred contemporaneously with decalcification which increased rock permeability and porosity. A second clay alteration event resulted in the precipitation of hydrothermal 1M illite which replaced hydrothermal kaolinite and is associated with gold deposition. Silver and silica deposition is also associated with this phase of hydrothermal alteration. Hydrothermal alteration was followed by supergene alteration which resulted in the formation of supergene kaolinite, halloysite, and smectite as well as the oxidation of iron-bearing minerals. Supergene clays are concentrated along faults, dike margins, and within rocks containing carbonate. Gold mineralization is not associated with supergene clay minerals within the Genesis and Blue Star deposits. Rocks classified as silicic-argillic in the Popovich Formation represent the most significant gold host. Silicicargillic rocks commonly exhibit bedding-parallel alteration zones. This pattern of alteration indicates that stratigraphy as well as northwest-trending structures played a significant role in the migration of gold-bearing fluids. Based on K-Ar age determinations of hydrothermal 1M illite associated with gold, the main event of mineralization in the Genesis and Blue Star deposits occurred between 93 and 100 Ma, during mid-Cretaceous time.
Strain Rate and Stress Relaxation Effects on Pressuremeter Testing in Clays
1992-03-01
CHARACTERISTICS OF KAOLINITE AND GROUND SILICA 245 APPENDIX E COMPUTER PROGRAMS ....................... 248 0 0 0 0 0 0 0 iv LIST OF TABLES Table Page 3.1 A...Comparison of Three Types of Boundary Conditions in a Multiaxial Cubical Test Apparatus ................... 37 3.2 Properties of the Kaolinite and Kaolin...to 0.01 %/min Versus Strain Rate for Kaolinite Clay ................... 102 4.3 Shear Strength Normalized with Respect to 0.01 %/min Versus Strain Rate
2013-09-30
HPMM. For these minerals, kaolinite and smectite , the corresponding shear speed estimates are 13 m/s and 0.25 m/s. The third and fourth columns of...representative value for each parameter in two clay minerals, kaolinite and smectite , which are the most common types in marine mud. These values produce...13 m/s for kaolinite and 0.25 m/s for smectite . The third column shows typical ranges of values for h, L, and χ in the two clay types. The fourth
Gibson, T.G.; Bybell, L.M.; Mason, D.B.
2000-01-01
Kaolinite usually is present in relatively small amounts in most upper Paleocene and lower Eocene neritic deposits of the northern US Atlantic Coastal Plain. However, there is a short period (less than 200,000 k.y.) in the latest Paleocene (upper part of calcareous nannoplankton Zone NP 9) when kaolinite-dominated clay mineral suites replaced the usual illite/smectite-dominated suites. During this time of global biotic and lithologic changes, kaolinite increased from less than 5% of the clay mineral suite to peak proportions of 50-60% of the suite and then returned to less than 5% in uppermost Paleocene/lowermost Eocene strata. This kaolinite pulse is present at numerous localities from southern Virginia to New Jersey. These sites represent both inner and middle neritic depositional environments and reflect input from several river drainage systems. Thus, it is inferred that kaolinite-rich source areas were widespread in the northeastern US during the latest Paleocene. Erosion of these source areas contributed the kaolinite that was transported and widely dispersed into shelf environments of the Salisbury embayment. The kaolinite increase, which occurred during a time of relatively high sea level, probably is the result of intensified weathering due to increased temperature and precipitation. The southern extent of the kaolinite pulse is uncertain in that uppermost Paleocene beds have not been identified in the southern Atlantic Coastal Plain. The late Paleocene kaolinite pulse that consists of an increase to peak kaolinite levels followed by a decrease can be used for detailed correlation between more upbasin and more downbasin sections in the Salisbury embayment. Correlations show that more upbasin Paleocene/Eocene boundary sections are erosionally truncated. They have varying portions of the kaolinite increase and, if present at all, discontinuous portions of the subsequent kaolinite decrease. As these truncated sections are disconformably overlain by lower Eocene strata, rapid erosional removal of large parts of the most kaolinite-rich P/E boundary clay deposits occurred by early Eocene time. Erosion of the kaolinite-rich P/E boundary beds was enhanced during times of sea-level fall when kaolinite-rich sediments were redeposited to produce kaolinite spikes in basal beds of lower and middle Eocene sequences that have little or no kaolinite elsewhere in the sequence. In contrast, more downbasin sites document only the upper, decreasing part of the kaolinite pulse. The absence of strata documenting the earlier kaolinite increase is attributed to slow sedimentation (condensed interval) as a result of a significant sea level rise that ponded most sediments in shallower waters, combined with the probable subsequent erosional removal of these thin downbasin deposits by oceanic currents.
Ugochukwu, Uzochukwu C; Fialips, Claire I
2017-07-01
Acid treatment of clay minerals is known to modify their properties such as increase their surface area and surface acidity, making them suitable as catalysts in many chemical processes. However, the role of these surface properties during biodegradation processes of polycyclic aromatic hydrocarbons (PAHs) is only known for mild acid (0.5 M Hydrochloric acid) treated clays. Four different clay minerals were used for this study: a montmorillonite, a saponite, a palygorskite and a kaolinite. They were treated with 3 M hydrochloric acid to produce acid activated clay minerals. The role of the acid activated montmorillonite, saponite, palygorskite and kaolinite in comparison with the unmodified clay minerals in the removal of PAHs during biodegradation was investigated in microcosm experiments. The microcosm experiments contained micro-organisms, oil, and clays in aqueous medium with a hydrocarbon degrading microorganism community predominantly composed of Alcanivorax spp. Obtained results indicated that acid activated clays and unmodified kaolinite did not enhance the biodegradation of the PAHs whereas unmodified montmorillonite, palygorskite and saponite enhanced their biodegradation. In addition, unmodified palygorskite adsorbed the PAHs significantly due to its unique channel structure. Copyright © 2017 Elsevier Ltd. All rights reserved.
Fogler, H. Scott; Srinivasan, Keeran R.
1990-01-01
A novel modified clay sorbent and method of treating industrial effluents to remove trace pollutants, such as dioxins, biphenyls, and polyaromatics such as benzo(a)pyrene and pentachlorophenol. The novel clay sorbent has a composite structure in which the interlayer space of an expandable clay, such as smectite, is filled with polyvalent or multivalent inorganic cations which forces weaker surfactant cations to locate on the surface of the clay in such an orientation that the resulting composite is hydrophilic in nature. A specific example is cetylpyridinium-hydroxy aluminum-montmorillonite. In certain embodiments, a non-expanding clay, such as kaolinite, is used and surfactant cations are necessarily located on an external surface of the clay. A specific example is cetylpyridinium-kaolinite.
Role of Organic Acids in Bioformation of Kaolinite: Results of Laboratory Experiments
NASA Astrophysics Data System (ADS)
Bontognali, T. R. R.; Vasconcelos, C.; McKenzie, J. A.
2012-04-01
Clay minerals and other solid silica phases have a broad distribution in the geological record and greatly affect fundamental physicochemical properties of sedimentary rocks, including porosity. An increasing number of studies suggests that microbial activity and microbially produced organic acids might play an important role in authigenic clay mineral formation, at low temperatures and under neutral pH conditions. In particular, early laboratory experiments (Linares and Huertas, 1971) reported the precipitation of kaolinite in solutions of SiO2 and Al2O3 with different molar ratios SiO2/Al2O3, together with fulvic acid (a non-characterized mixture of many different acids containing carboxyl and phenolate groups) that was extracted from peat soil. Despite many attempts, these experiments could not be reproduced until recently. Fiore et al. (2011) hypothesized that the non-sterile fulvic acid might have contained microbes that participated in the formation of kaolinite. Using solutions saturated with Si and Al and containing oxalate and/or mixed microbial culture extracted from peat-moss soil, they performed incubation experiments, which produced kaolinite exclusively in solutions containing oxalate and microbes. We proposed to test the role of specific organic acids for kaolinite formation, conducting laboratory experiments at 25˚C, with solutions of sodium silicate, aluminum chloride and various organic compounds (i.e. EDTA, citric acid, succinic acid and oxalic acid). Specific organic acids may stabilize aluminum in octahedral coordination positions, which is crucial for the initial nucleation step. In our experiments, a poorly crystalline mineral that is possibly a kaolinite precursor formed exclusively in the presence of succinic acid. In experiments with other organic compounds, no incorporation of Al was observed, and amorphous silica was the only precipitated phase. In natural environments, succinic acid is produced by a large variety of microbes as an intermediate product of the tricarboxylic acid cycle. Our results demonstrate, for the first time, that the formation of a specific clay mineral (proto-kaolinite) occurs in the presence of a specific organic compound (succinic acid). This implies that microbial species capable of excreting succinate among their EPS may promote authigenic kaolinite formation at low temperature and neutral pH. This biological degradation process might play a crucial role for the formation of authigenic kaolinite, which is a widespread clay mineral in sedimentary environments. Fiore, S., Dumontet, S., Huertas, F.J., and Pasquale, V., 2011. Bacteria-induced crystallization of kaolinite. Applied Clay Science, 53:566-571. Linares, J., and Huertas, F., 1971. Kaolinite: Synthesis at room temperature. Science 171: 896-897.
Geology and Refractory Clay Deposits of the Haldeman and Wrigley Quadrangles, Kentucky
Patterson, Sam H.; Hosterman, John W.; Huddle, John Warfield
1962-01-01
The Haldeman and Wrigley 7th-minute quadrangles are near the western edge of the eastern Kentucky coal field and cover an area of approximately 117 square miles in parts of Carter, Rowan, Elliott, and Morgan Counties, Ky. The rocks exposed in the two quadrangles are of Early and Late Mississippian and Early and Middle Pennsylvanian age. The Mississippian rocks are composed of the thick Brodhead formation, which consists of siltstone and shale, and eleven thin marine limestone and shale formations, having an aggregate thickness of about 150 feet. The Lee and Breathitt formations, of Pennsylvanian age, consist of sandstone, siltstone, and shale; they also contain thin beds of coal and several beds of underclay, including the economically important Olive Hill clay bed of Crider, 1913. Pennsylvanian rocks include beds of both continental and marine origin. The eleven thin Mississippian formations and the upper-most part of the thick Brodhead formation are truncated by a prominent unconformity on which rocks of Pennsylvanian age rest. The rocks occupy a region of gentle dips between the Cincinnati arch and the Appalachian Mountains. Refractory clay deposits are in the Olive Hill clay bed, which occurs in the lower part of the Lee formation. The Olive Hill clay bed is discontinuous and consists of a series of irregularly shaped lenses. The bed is approximately two-thirds semifiint clay and one-third flint clay, and it contains minor amounts of plastic clay. Some of the flint clay is nearly pure kaolinite, but the semi flint and plastic clay consists of mixtures of kaolinite, illite, and mixed-layer clay minerals. The structure of the kaolinite ranges from highly crystalline to very poorly crystalline 'fireclay' type. The degree of crystallinity of the kaolinite and the hardness of the clay vary inversely with the amount of illite and mixed-layer clay minerals present. The nearly pure kaolinite is believed to have formed by the removal of alkalies and some silica fram mixtures of kaolinite, illite, and mixed-layer clays by leaching in swamps to the deposition of the beds overlying the clay. The refractory properties of the clay vary directly with the purity of the kaolinite, and refractoriness decreases as the proportions of illite and mixed-layer clays increase. Certain nonclay minerals, chiefly siderite, pyrite, and iron oxide-bearing minerals, also act as fiuxes, reducing the refractory properties of the clay. The entire resources of clay in the Olive Hill clay bed are roughly and tentatively estimated to include 105,000,000 tons in the Haldeman quadrangle and 175,000,000 tons in the Wrigley quadrangle. Much of this clay is of poor quality and the amount that is better than the minimum requirements for use in refractories is probably about 30,000,000 tons. Only a fraction of this tonnage is suitable for superheat-duty products. Limestone is the only nonmetallic mineral resource other than refractory clay that has been developed in the two quadrangles, but 1arge amounts of shale suitable for use in making lightweight aggregate and structural clay products may also be present. Most of the limestone, which is quarried. in both quadrangles, is used for road-metal, concrete aggregate, and agriculture stone, but some of the limestone is of the quality that would be suitable for other uses. Virtually all the Mississippian Beech Creek limestone of Malott, 1919 which is as much as 18 feet thick, consists of high-calcium limestone. Shale beds that appear most favoralble for making lightweight aggregate are in the shale facies of the Lee formation of Pennsylvanian age. Shale that is probably suitable for structural clay products is present in the shale flacles of the Lee formation and in the Muldraugh formation of Mississippian age. Several dry holes have been drilled in search for oil and gas within the area of the two quadrangles. Though no commercial production was ever attained, one well furnished a supply of gas f
Surface charge features of kaolinite particles and their interactions
NASA Astrophysics Data System (ADS)
Gupta, Vishal
Kaolinite is both a blessing and a curse. As an important industrial mineral commodity, kaolinite clays are extensively used in the paper, ceramic, paint, plastic and rubber industries. In all these applications the wettability, aggregation, dispersion, flotation and thickening of kaolinite particles are affected by its crystal structure and surface properties. It is therefore the objective of this research to investigate selected physical and surface chemical properties of kaolinite, specifically the surface charge of kaolinite particles. A pool of advanced analytical techniques such as XRD, XRF, SEM, AFM, FTIR and ISS were utilized to investigate the morphological and surface chemistry features of kaolinite. Surface force measurements revealed that the silica tetrahedral face of kaolinite is negatively charged at pH>4, whereas the alumina octahedral face of kaolinite is positively charged at pH<6, and negatively charged at pH>8. Based on electrophoresis measurements, the apparent iso-electric point for kaolinite particles was determined to be less than pH 3. In contrast, the point of zero charge was determined to be pH 4.5 by titration techniques, which corresponds to the iso-electric point of between pH 4 and 5 as determined by surface force measurements. Results from kaolinite particle interactions indicate that the silica face--alumina face interaction is dominant for kaolinite particle aggregation at low and intermediate pH values, which explains the maximum shear yield stress at pH 5-5.5. Lattice resolution images reveal the hexagonal lattice structure of these two face surfaces of kaolinite. Analysis of the silica face of kaolinite showed that the center of the hexagonal ring of oxygen atoms is vacant, whereas the alumina face showed that the hexagonal surface lattice ring of hydroxyls surround another hydroxyl in the center of the ring. High resolution transmission electron microscopy investigation of kaolinite has indicated that kaolinite is indeed composed of silica/alumina bilayers with a c-spacing of 7.2 A. The surface charge densities of the silica face, the alumina face and the edge surface of kaolinite all influence particle interactions, and thereby affect the mechanical properties of kaolinite suspensions. The improved knowledge of kaolinite surface chemistry from this dissertation research provides a foundation for the development of improved process strategies for both the use and disposal of clay particles such as kaolinite.
1997-05-01
estuaries was modeled using phenanthrene, bacterial extracellular polymer and kaolinite clay as surrogates for a hydrophobic organic pollutant...coefficients obtained for phenanthrene sorption to kaolinite and bentonite in the presence of varying amounts of DOM represented by alginic acid and tannic...acid. 333 Table B.3: Literature values for sorption between phenanthrene, humic acid and kaolinite for [DOM]a = 10 mg/L 334 Table E.1: Sample output data
Creep and Sliding in Clays Slopes: Mutual Effects of Interlayer Swelling and Ice Jacking.
1984-01-11
chlorite 14% (6-21%) calcite 6,5% (1 - 15%) kaolinite 2% ( 1- 5%) dolomite 0,5% (0 - 4%) montmorillonite 23% (15-35%) Non clay phases 19% (15-30%) Clay...iconcretions, 200 mm coal lenses RE 3 4 Calcite N Quartz Feldspar Illite-muscovite Z Chlorite E Kaolinite montmori 1 loni te Fig. 10: Mineral content... montmorillonite , belong to a fluviatile fresh water cycle and are possibly influenced by volcanic ash falls. The series under investigation belongs to the upper
DOE Office of Scientific and Technical Information (OSTI.GOV)
Destaillats, Hugo; Kibanova, D.; Trejo, M.
2008-03-01
We studied the synthesis and photocatalytic activity of small-sized TiO{sub 2} supported on hectorite and kaolinite. Deposition of TiO{sub 2} on the clay mineral surface was conducted by using a sol-gel method with titanium isopropoxide as precursor. Anatase TiO{sub 2} particles formation was achieved by hydrothermal treatment at 180 C. Material characterization was conducted using XRD, SEM, XPS, ICP-OES, BET and porosimetry analysis. Efficiency in synthesizing clay-TiO{sub 2} composites depended strongly on the clay mineral structure. Incorporation of anatase in hectorite, an expandable clay mineral, was found to be very significant (> 36 wt.% Ti) and to be followed bymore » important structural changes at the clay mineral surface. Instead, no major structural modifications of the clay were observed for kaolinite-TiO{sub 2}, as compared with the untreated material. Photocatalytic performance of clay-TiO{sub 2} composites was evaluated with ATR-FTIR following the oxidation of adsorbed toluene and d-limonene, two model air pollutants. In either case, the photocatalytic removal efficiency of these hydrophobic substrates by the synthesized clay-TiO{sub 2} composites was comparable to that observed using pure commercial TiO{sub 2} (Degussa P25).« less
Slime coating of kaolinite on chalcopyrite in saline water flotation
NASA Astrophysics Data System (ADS)
Li, Zhi-li; Rao, Feng; Song, Shao-xian; Li, Yan-mei; Liu, Wen-biao
2018-05-01
In saline water flotation, the salinity can cause a distinguishable slime coating of clay minerals on chalcopyrite particles through its effect on their electrical double layers in aqueous solutions. In this work, kaolinite was used as a representative clay mineral for studying slime coating during chalcopyrite flotation. The flotation of chalcopyrite in the presence and absence of kaolinite in tap water, seawater, and gypsum-saturated water and the stability of chalcopyrite and kaolinite particles in slurries are presented. Zeta-potential distributions and scanning electron microscopy images were used to characterize and explain the different slime coating degrees and the different flotation performances. Kaolinite particles induced slime coating on chalcopyrite surfaces and reduced chalcopyrite floatability to the greatest extent when the pH value was in the alkaline range. At 0.24wt% of kaolinite, the chalcopyrite floatability was depressed by more than 10% at alkaline pH levels in tap water. Salinity in seawater and gypsum-saturated water compressed the electrical double layers and resulted in extensive slime coating.
Intercalation of acrylic acid and sodium acrylate into kaolinite and their in situ polymerization
NASA Astrophysics Data System (ADS)
Zhang, Bo; Li, Yanfeng; Pan, Xiaobing; Jia, Xin; Wang, Xiaolong
2007-02-01
Novel nano-composites of poly (acrylic acid)-kaolinite were prepared, and intercalation and in situ polymerization were used in this process. The nano-composites were obtained by in situ polymerization of acrylic acid (AA) and sodium acrylate (AANa) intercalated into organo-kaolinite, which was obtained by refining and chemically modifying with solution intercalation step in order to increase the basal plane distance of the original clay. The modification was completed by using dimethyl-sulfoxide (DMSO)/methanol and potassium acetate (KAc)/water systems step by step. The materials were characterized with the help of XRD, FT-IR and TEM; the results confirmed that poly(acrylic acid) (PAA) and poly(sodium acrylate) (PAANa) were intercalated into the interlamellar spaces of kaolinite, the resulting copolymer composites (CC0 : copolymer crude kaolinite composite, CC1 : copolymer DMSO kaolinite composite, CC2 : copolymer KAc kaolinite composite) of CC2 exhibited a lamellar nano-composite with a mixed nano-morphology, and partial exfoliation of the intercalating clay platelets should be the main morphology. Finally, the effect of neutralization degree on the intercalation behavior was also investigated.
Johnsson, Mark J.; Ellen, Stephen D.; McKittrick, Mary Anne
1993-01-01
Orographic precipitation on the southern flank of the southeastern Koolau Mountains produces a pronounced precipitation gradient. The corresponding gradient in the intensity of the chemical weathering environment provides an opportunity to address the effects of varying chemical weathering intensity on the composition of clay-size weathering products in soils developed on basalt. In addition, little-modified remnants of the constructional surface of the Koolau Volcano, isolated by stream dissection, remain as facets on the southern ends of the parallel ridges of the study area. By comparing clay mineralogy of soils developed on these older geomorphic surfaces with those developed on the younger sharp-crested ridges and steep side slopes, the effects of weathering duration on clay mineralogy can also be addressed.Soil clays in this part of the Koolau Mountains are mineralogically complex; principal phases include smectite, kaolinite, and halloysite, but pure end member phases are uncommon. Rather, most phases contain some amount of mixed layering. Smectite may contain small (<5%) amounts of randomly interstratified halloysite. Similarly, kaolinite commonly contains a small proportion of halloysite interlayers. A complex halloysitic phase shows evidence of interstratification with both smectite and kaolinite. Nonphyllosilicates found in the clay fraction include gibbsite, goethite, rare quartz, and perhaps cristobalite.The gradient in precipitation is reflected in soil clay mineralogy by varying proportions of dominantly smectitic, kaolinitic, and halloysitic phases. In regions of relatively low precipitation (<2,000 mm/yr), soils are dominated by the smectitic and halloysitic phases. With increased precipitation (as much as ∼4,000 mm/yr), kaolinitic and halloysitic phases become the dominant clay minerals, and goethite and gibbsite become increasingly abundant.Older soils developed on geomorphic surfaces representing the original constructional surface of Koolau Volcano are markedly more leached than those from younger landscapes in the same precipitation regime. Although smectite may be present, kaolinite is the dominant phase, and accumulations of Fe and Ti occur in the uppermost soil levels. Enrichment of Zr and Ti in these soils, as compared to concentrations in the original basaltic parent material, indicates that as much as 75% of the parent material has been lost. Thus weathering duration may affect soil clay composition in the same way as weathering intensity.Because smectite and halloysite are expandable clay minerals, their presence in soils may decrease slope stability and influence the nature of slope processes. Soil avalanches occur on steep slopes throughout the study area, whereas slow-moving landslides appear to be restricted to gentler slopes in drier parts of the study area where smectite is abundant. The clay mineralogy of soils thus appears to influence the nature of slope processes in the southeastern Koolau Mountains.
Intensity of African Humid Periods Estimated from Saharan Dust Fluxes.
Ehrmann, Werner; Schmiedl, Gerhard; Beuscher, Sarah; Krüger, Stefan
2017-01-01
North Africa experienced dramatic changes in hydrology and vegetation during the late Quaternary driven by insolation-induced shifts of the tropical rain belt and further modulated by millennial-scale droughts and vegetation-climate feedbacks. While most past proxy and modelling studies concentrated on the temporal and spatial dynamics of the last African humid period, little is known about the intensities and characteristics of pre-Holocene humid periods. Here we present a high-resolution record of fine-grained eastern Saharan dust from the Eastern Mediterranean Sea spanning the last 180 kyr, which is based on the clay mineral composition of the marine sediments, especially the kaolinite/chlorite ratio. Minimum aeolian kaolinite transport occurred during the African Humid Periods because kaolinite deflation was hampered by increased humidity and vegetation cover. Instead, kaolinite weathering from kaolinite-bearing Cenozoic rocks was stored in lake basins, river beds and soils during these periods. During the subsequent dry phases, fine-grained dust was mobilised from the desiccated lakes, rivers and soils resulting in maximum aeolian uptake and transport of kaolinite. The kaolinite transport decreased again when these sediment sources exhausted. We conclude that the amount of clay-sized dust blown out of the Sahara into the Eastern Mediterranean Sea is proportional to the intensity of the kaolinite weathering and accumulation in soils and lake sediments, and thus to the strength of the preceding humid period. These humid periods provided the windows for the migration of modern humans out of Africa, as postulated previously. The strongest humid period occurred during the Eemian and was followed by two weaker phases centred at ca. 100 ka and ca. 80 ka.
Intensity of African Humid Periods Estimated from Saharan Dust Fluxes
Ehrmann, Werner; Schmiedl, Gerhard; Beuscher, Sarah; Krüger, Stefan
2017-01-01
North Africa experienced dramatic changes in hydrology and vegetation during the late Quaternary driven by insolation-induced shifts of the tropical rain belt and further modulated by millennial-scale droughts and vegetation-climate feedbacks. While most past proxy and modelling studies concentrated on the temporal and spatial dynamics of the last African humid period, little is known about the intensities and characteristics of pre-Holocene humid periods. Here we present a high-resolution record of fine-grained eastern Saharan dust from the Eastern Mediterranean Sea spanning the last 180 kyr, which is based on the clay mineral composition of the marine sediments, especially the kaolinite/chlorite ratio. Minimum aeolian kaolinite transport occurred during the African Humid Periods because kaolinite deflation was hampered by increased humidity and vegetation cover. Instead, kaolinite weathering from kaolinite-bearing Cenozoic rocks was stored in lake basins, river beds and soils during these periods. During the subsequent dry phases, fine-grained dust was mobilised from the desiccated lakes, rivers and soils resulting in maximum aeolian uptake and transport of kaolinite. The kaolinite transport decreased again when these sediment sources exhausted. We conclude that the amount of clay-sized dust blown out of the Sahara into the Eastern Mediterranean Sea is proportional to the intensity of the kaolinite weathering and accumulation in soils and lake sediments, and thus to the strength of the preceding humid period. These humid periods provided the windows for the migration of modern humans out of Africa, as postulated previously. The strongest humid period occurred during the Eemian and was followed by two weaker phases centred at ca. 100 ka and ca. 80 ka. PMID:28129378
DOE Office of Scientific and Technical Information (OSTI.GOV)
Guerra, Denis L., E-mail: denis@cpd.ufmt.b; Leidens, Victor L.; Viana, Rubia R.
2010-05-15
The compound N{sup 1}-[3-(trimethoxysilyl)propyl]diethylenetriamine was anchored onto Amazon kaolinite surface by heterogeneous route. The modified and natural kaolinite samples were characterized by transmission electron microscopy, scanning electron microscopic, X-ray diffraction, and nuclear magnetic nuclei of {sup 29}Si and {sup 13}C. The well-defined peaks obtained in the {sup 13}C NMR spectrum in the 5.0-62.1 ppm region confirmed the attachment of organic functional groups as pendant chains bonded into the porous clay. The ability of these materials to remove U(VI) from aqueous solution was followed by a series of adsorption isotherms adjusted to a Sips equation at room temperature and pH 4.0.more » The kinetic parameters analyzed by the Lagergren and Elovich models gave a good fit for a pseudo-second order reaction with k{sub 2} values 16.0 and 25.1 mmol g{sup -1} min{sup -1} ranges for natural and modified kaolinite clays, respectively. The energetic effects caused by metal ion adsorption were determined through calorimetric titrations. - Graphical abstract: This investigation reports the use of original and modified kaolinites as alternative absorbents. The compound N-[3-trimethoxysilyl)propyl]diethylenetriamine was anchored onto Amazon kaolinite surface by heterogeneous route.« less
NASA Astrophysics Data System (ADS)
Dumon, Mathijs; Oostermeyer, Fran; Timmermans, Els; De Meulemeester, Aschwin; Mees, Florias; Van Driessche, Isabel; Erens, Hans; Bazirake Mujinya, Basile; Van Ranst, Eric
2015-04-01
The study of the formation and transformation of clay minerals is of the upmost importance to understand soil formation and to adjust land-use management to the land surface conditions. These clay minerals determine to a large extent the soil physical and chemical properties. It is commonly observed that over time the mineralogy of any parent material is transformed to a simple assemblage composed mostly of Al and Fe oxides and low-activity clays, e.g. kaolinite. This is especially obvious in the humid tropics, which have been protected from glacial erosion, allowing deep, highly weathered soils to form. Despite the abundant presence of kaolinite in these soils, its formation pathways are still under debate: either neoformation by dissolution-crystallisation reactions or solid-state transformation of 2:1 phyllosilicates. To elucidate this, weathering sequences in a unique 40 m core taken below a termite mound, reaching a talc-chlorite bearing substrate in the Lubumbashi area, Katanga, DR Congo are being investigated in detail using a.o. quantitative X-ray diffraction analysis, chemical characterization, micromorphology and µXRF-scanning with the main objective to improve the understanding of the formation pathways of kaolinite subgroup minerals in humid tropical environments. Based on an initial characterization of the core, two zones of interest were selected for more detailed analysis, for which the early findings will be presented. The first zone extends from ca. 9 m to 11 m below the surface is dominated by kaolinite but shows early traces of primary talc and micas. The second zone extends from 34 to 36 m below the surface and contains large amounts of chlorite, with smaller amounts of talc, micas and kaolinite.
Interaction between ATP, metal ions, glycine, and several minerals
NASA Technical Reports Server (NTRS)
Rishpon, J.; Ohara, P. J.; Lawless, J. G.; Lahav, N.
1982-01-01
Interactions between ATP, glycine and montmorillonite and kaolinite clay minerals in the presence of various metal cations are investigated. The adsorption of adenine nucleotides on clays and Al(OH)3 was measured as a function of pH, and glycine condensation was followed in the presence of ATP, ZnCl2, MgCl2 and either kaolinite or montmorillonite. The amounts of ATP and ADP adsorbed are found to decrease with increasing Ph, and to be considerably enhanced in experiments with Mg(2+)- and Zn(2+)-montmorillonite with respect to Na(+)-montmorillonite. The effects of divalent cations are less marked in kaolinite. Results for Al(OH)3 show the importance of adsorption at clay platelet edges at high pH. The decomposition of ATP during drying at high temperature is observed to be inhibited by small amounts of clay, vacuum, or Mg(2+) or Zn(2+) ions, and to be accompanied by peptide formation in the presence of glycine. Results suggest the importance of Zn(2+) and Mg(2+) in chemical evolution.
Ocurrence and genesis of kaolinite in sedimentary deposits from the Southern Iberian Range (Spain)
NASA Astrophysics Data System (ADS)
Bauluz, B.; Mayayo, M. J.; Yuste, A.; Fernández-Nieto, C.; González López, J. M.
2003-04-01
The kaolinite-rich clay deposits from the Southern Iberian Range (Spain) correspond to continental clay-sandy series developed during Lower Cretaceous times. The clay deposits are mined by ceramic industry nowadays, and are intercalated with coal levels (lignites) that are also mined for energetic purposes. We have characterized by XRD, optical, and electronic microscopy (SEM, TEM) the mineralogical composition of a set of 55 samples, emphasizing in the kaolinite features: texture, morphology, crystallinity, and composition. Studied rocks (lutites, limolites, and sandstones) are composed by different proportions of quartz, kaolinite, muscovite, and illite, with minor K-feldspar, pyrite and siderite. The XRD study shows that, in comparison to micaceous phases, kaolinite particles are preferentially concentrated in the finest fractions of the rocks, indicating a lower crystal size. In addition, electron microscopy observations show that kaolinite occurs in four distinct modes: (a) as subhedral-anhedral flakes (<20 μm) that are the major component of the lutites. This kaolinite shows a disordered type (XRD). Chemical composition of kaolinite and illite particles (TEM/AEM) show a broad compositional variation. Some of the particles correspond to kaolinite and illite compositions, but most of the analyses indicate intermediate compositions, suggesting the occurrence of submicroscopic intergrowths of kaolinite and illite. The detection of low Ca contents in some analyses indicate the presence of smectite phases in these intergrowths. Probably, this kaolinite was formed by alteration of aluminosilicates (micas and K-feldspars) in the source area of the sediments. (b) as flakes filling pyritized plants in some dark lutites. (c) as subhedral and hexagonal plates, up to 5 μm in size, in sandstones. They are replacing K-feldspar fragments with clear evidence of alteration under SEM. The kaolinites display a high degree of order. (d) as booklets of pseudo-hexagonal plates of kaolinite and muscovite-type mica. These aggregates, up to 30 μm thick, appears mainly in limolites. The growth of kaolinite between the cleavage layers of pre-existing detrital mica resulted in a net increase in volume of the original grain. The delicate fabrics of these intergrowths suggest an in situ origin. The modes (b), (c) and (d) would have an authigenic origin, being K-feldspar one of the source of components for their formation during the early stages of the diagenesis.
Saeedi, Mohsen; Li, Loretta Y; Grace, John R
2018-05-15
The effects of soil components such as clay minerals and as humic acids, as well as co-existing metals and polycyclic aromatic hydrocarbons, on desorption and mobility are examined. Three types of artificially blended clay and clay mineral mixtures (pure kaolinite, kaolinite + sand and kaolinite + sand + bentonite), each with different humic acid content, were tested for desorption and mobility of acenaphthene, fluorene and fluoranthene by three extracting solutions CaCl 2 (0.01 M) and EDTA (0.01M) with non-ionic surfactants (Tween 80 and Triton X100). Heavy metals (Ni, Pb and Zn) were also studied for desorption and mobility. The influence of co-present metals on simultaneous desorption and mobility of PAHs was investigated as well. The results showed that <10% of metals in the clay mineral mixtures were mobile. Combined EDTA and non-ionic solutions can enhance the desorption and mobility of PAHs to >80% in clay mineral mixtures containing no sand, while in the same soils containing ∼40% sand, the desorption exceeded 90%. Heavy metals, as well as increasing humic acids content in the clay mineral mixtures, decreased the desorption and mobility of PAHs, especially for soils containing no sand, and for fluoranthene compared with fluorene and acenaphthene. Copyright © 2018 Elsevier Ltd. All rights reserved.
NASA Astrophysics Data System (ADS)
Chizhikova, N. P.; Gamzikov, G. P.; Chechetko, E. S.
2018-01-01
The mineralogical composition of agrogray, dark gray, and agro-dark gray soils (Luvic Greyzemic Retic Phaeozems); agro-dark gray residual-calcareous soils (Calcaric Cambic Phaeozems); clay-illuvial agrochernozems (Luvic Chernic Phaeozems); and agrochernozems with migrational-mycelial carbonates (Haplic Chernozems) developed in the forest-steppe of Central Siberia within the Irkutsk Depression has been studied. The clay (<1 μm) fraction separated from these soils consists of mixed-layer minerals with alternating layers of hydromica, smectite, vermiculite, and chlorite; the proportions between them change within the soil profiles. The clay fraction also contains hydromicas, kaolinite, chlorite, and some admixture of the fine-dispersed quartz. Each type of the soils is characterized by its own distribution pattern of clay material with specific alternation of layers in the mixed-layer formations. Mixed-layer minerals of the chlorite-vermiculite type predominate in the upper horizons of texture-differentiated soils. Down the soil profile, the content of mixed-layer mica-smectitic minerals increases. In the clay fraction of arable dark gray-humus soils with residual carbonates, the distribution of the clay fraction and major mineral phases in the soil profile is relatively even. An increased content of well-crystallized kaolinite is typical of these soils. The parent material of agrochernozems has a layered character: the upper horizons are generally depleted of clay, and the middle-profile and lower horizons are characterized by the considerable kaolinite content. In general, the clay material of soils of the Tulun-Irkutsk forest-steppe differs considerably from the clay material of foreststeppe soils developed from loesslike and mantle loams in the European part of Russia. In particular, this difference is seen in the proportions between major mineral phases and between biotitic and muscovitic components, as well as in the degree of crystallinity and behavior of kaolinite and chlorite.
NASA Astrophysics Data System (ADS)
Guerra, Denis L.; Leidens, Victor L.; Viana, Rúbia R.; Airoldi, Claudio
2010-05-01
The compound N 1-[3-(trimethoxysilyl)propyl]diethylenetriamine was anchored onto Amazon kaolinite surface by heterogeneous route. The modified and natural kaolinite samples were characterized by transmission electron microscopy, scanning electron microscopic, X-ray diffraction, and nuclear magnetic nuclei of 29Si and 13C. The well-defined peaks obtained in the 13C NMR spectrum in the 5.0-62.1 ppm region confirmed the attachment of organic functional groups as pendant chains bonded into the porous clay. The ability of these materials to remove U(VI) from aqueous solution was followed by a series of adsorption isotherms adjusted to a Sips equation at room temperature and pH 4.0. The kinetic parameters analyzed by the Lagergren and Elovich models gave a good fit for a pseudo-second order reaction with k2 values 16.0 and 25.1 mmol g -1 min -1 ranges for natural and modified kaolinite clays, respectively. The energetic effects caused by metal ion adsorption were determined through calorimetric titrations.
Mixed-layer kaolinite-montmorillonite from the Yucatan Peninsula, Mexico
Schultz, L.G.; Shepard, A.O.; Blackmon, P.D.; Starkey, H.C.
1971-01-01
Clay beds 1–2 m thick and interbedded with marine limestones probably of early Eocene age are composed of nearly pure mixed-layer kaolinite-montmorillonite. Particle size studies, electron micrographs, X-ray diffraction studies, chemical analyses, cation exchange experiments, DTA, and TGA indicate that clays from three different localities contain roughly equal proportions of randomly interlayered kaolinite and montmorillonite layers. The montmorillonite structural formulas average K0·2Na0·2Ca0·2Mg0·2(Al2·5Fe1·03+Mg0·5)(Al0·75Si7.25)O20+(OH)4−, with a deficiency of structural (OH) in either the montmorillonite or kaolinite layers. Nonexchangeable K+ indicates that a few layers are mica-like. Crystals are mostly round plates 1/10 to 1/20 µ across. The feature most diagnostic of the mixed-layer character is an X-ray reflection near 8 Å after heating at 300°C. The clays are inferred to have developed by weathering of volcanic ash and subsequent erosion and deposition in protected nearshore basins.
NASA Astrophysics Data System (ADS)
CHEN, Q.; Liu, Z.; Stattegger, K.
2012-12-01
Clay mineralogy of two gravity cores (18428 and 18429) on the upper continental slope of the northwestern South China Sea was investigated in order to understand terrigenous sediment sources and to evaluate the contribution from the Red River since the Late Glacial Maximum. Planktonic foraminiferal oxygen isotope and carbonate stratigraphies suggest that Core 18428 is constrained in Holocene while Core 18429 covers the period of MIS 1-2. Clay mineral assemblages of two cores are composed mainly of smectite (18-57%) and illite (21-41%), with minor chlorite (12-21%) and kaolinite (8-26%). In despite of relatively constant values of illite crystallinity, ranging among 0.14°-0.20° Δ2θ, the time series variation in clay mineral distributions indicates a strong glacial-interglacial shift. Contents of illite, chlorite, and kaolinite (Core 18429) in the Holocene are lower than in the glacial period, and vice versa for the smectite content. The provenance analysis based on clay mineralogy suggests the Red River as a predominant sedimentary source of illite, chlorite, and kaolinite during all the depositional period of MIS 1-2. The sea level change actually controlled the variations of clay mineral assemblages on the upper slope since the Last Glacial Maximum. When the sea level was low during the last glacial period, more terrigenous sediments from the Red River could reach the continental slope in the northwestern South China Sea. However, when the sea level is closed to the present situation during the Holocene, most of Red River sediments could be trapped in the Gulf of Tonkin, instead of draining in the deep South China Sea.
Clay mineral distribution and provenance in the Heuksan mud belt, Yellow Sea
NASA Astrophysics Data System (ADS)
Cho, Hyen Goo; Kim, Soon-Oh; Kwak, Kyeong Yoon; Choi, Hunsoo; Khim, Boo-Keun
2015-12-01
The Heuksan mud belt (HMB), located in the southeastern Yellow Sea, runs parallel to the southwest coast of Korea. In this study, the distribution and relative contribution of four major clay minerals are investigated using 101 surface sediment samples collected in the course of KIOST (2001, 2010, 2011) and KIGAM (2012) cruises, as well as 33 river sediment samples (four from the Huanghe River, three from the Changjiang River, and 26 from Korean rivers) in order to clarify the provenance of fine-grained sediments in the HMB. Based on this currently largest and most robust dataset available for interpretation, the clay mineral assemblages of the fine-grained sediments in the HMB are found to be on average composed of 64.7% illite, 17.9% chlorite, 11.4% kaolinite, and 5.9% smectite. Overall, the clay mineral assemblages are similar in both the northern and the southern parts of the HMB, although smectite seems to be relatively enriched in the southern part, whereas kaolinite is slightly more dominant in the northern part. This clearly indicates that the clays are mostly derived from Korean rivers and, in the southern part of the HMB, partly also from the Huanghe River in China. The new data thus confirm and strengthen the tentative interpretation of some earlier work based on a more limited dataset.
Ortiz, José; Montaño, Martín; Plascencia, Alejandro; Salinas, Jaime; Torrentera, Noemí; Zinn, Richard A.
2016-01-01
Two experiments were conducted to examine the influence of kaolinite clay supplementation (0%, 1%, or 2% diet dry matter [DM] basis) on characteristics of digestion (Trial 1) and growth performance (Trial 2) in calf-fed Holstein steers fed a finishing diet. In Trial 1, 6 Holstein steers (539±15 kg) with ruminal and duodenal cannulas were used to evaluate treatment effects on characteristics of digestion. Kaolinite clay supplementation decreased total tract DM digestion (linear effect, p<0.01) without effects (p≥0.10) on site and extent of digestion of organic matter, neutral detergent fiber, starch and N, or ruminal microbial efficiency. There were no treatment effects on ruminal pH, volatile fatty acids molar proportions or estimated methane production. In Trial 2, 108 Holstein steers (132.4±5.6 kg) were used in a 308-d study to evaluate growth performance and carcass characteristics. There were no treatment effects (p>0.10) on average daily gain (ADG) and gain efficiency (ADG/dry matter intake). Kaolinite supplementation tended (linear effect, p = 0.08) to increase dietary net energy (NE) during the initial 112-d period. However, the overall (308-d) effect of supplementation dietary NE was not appreciable (p>0.20). However, due to the inertness of kaolinite, itself, the ratio of observed-to-expected dietary NE increased with kaolinite supplementation. This effect was more pronounced (linear effect, p 0.03) during the initial 224 d of the study. Overall (308 d), kaolinite supplementation tended to increase (linear effect, p = 0.07) dietary NE by 3% over expected. Kaolinite supplementation did not affect carcass weight, yield grade, longissimus area, kidney, pelvic and heart fat, and quality grade, but decreased (linear effect, p = 0.01) dressing percentage. It is concluded that kaolinite supplementation up to 2% of diet DM may enhance energetic efficiency of calf-fed Holstein steers in a manner independent of changes in characteristics of ruminal and total tract digestion. PMID:27165016
Chlorination of alumina in kaolinitic clay
NASA Astrophysics Data System (ADS)
Grob, B.; Richarz, W.
1984-09-01
The chlorination of alumina in kaolinitic clay with Cl2 and CO gas mixtures was studied gravimetrically. The effects of the calcination method and of NaCl addition on the reactivity of the clay were examined. Fast reaction rates were achieved only with samples previously exposed to a sulfating treatment. Optimum conditions, with maximum yield and selectivity to A1C13 and minimum SiO2 conversion, were found between 770 and 970 K. At higher temperatures the SiCl4 formed poisons the reactive alumina surface by selective chemisorption with a marked decrease of the reaction rate.
Mineralogy and thermal properties of clay from Slatina (Ub, Serbia)
NASA Astrophysics Data System (ADS)
Milosevic, Maja; Logar, Mihovil; Kaludjerovic, Lazar; Jelic, Ivana
2017-04-01
The "Slatina" deposit, Ub, Serbia was opened in 1965 and represents one of few deposits exploited by "Kopovi" a.d., Ub, company. Deposit is composed of clay layers belonging to Neogene sediments that are widespread transgressive over granitoid rocks of Cer mountain and Paleozoic and Mesozoic sediments. Clay is mostly of illite-montmorillonite-kaolinite type and they are generally used as ceramic materials while some of the layers are used as fire-resistant materials. In this study we present mineralogical and thermal characterization of two samples to determine their application as industrial materials. Chemical and mineral composition was determined using inductively coupled plasma optical emission spectroscopy (ICP-OES), X-ray diffraction (XRD) on powder and oriented samples, infrared spectroscopy (IR) and granulometry. Cationic exchange capacity (CEC) and specific surface area (SSA) was determined using spectrophotometry and methylene blue (MB). Thermal properties where determined by gravimetry (120, 350, 600 and 1000 oC) and differential thermal analysis (DTA). Quantitative mineral composition obtained by Rietveld refinement of combined chemical and XRD data shows that the sample 1(SC) is mainly smectite-illite (45%) and kaolinite (14%) clay with 19% of quartz, 10% feldspars and 7% of limonite, while sample 2(SV) is smectite-illite (43%) and kaolinite (11%) clay with 10% of quartz, 15% feldspars and 7% of limonite. Both samples have low content of impurities (carbonate minerals). Medium grain size (μm) goes from 1.02 (SSA = 104 m2/g) for sample 1(SC) to 0.71 (SSA = 117 m2/g) for sample 2(SV) while their CEC is 12.7 and 14.9 mmol/100g for 1(SC) and 2(SV) respectively. IR spectra of the samples shows larger amount of smectite clays with quartz and carbonate minerals for both samples which is in accordance with XRD data. DTA data shows couple of events that are endothermic. First one (100-200 oC) is associated with loss of moisture and constitutive water, second (300-400 oC) with iron hydroxide minerals, third (500-600 oC) with smectite clay content with smaller separate bands of kaolinite clays while events between 800-900 oC correspond to carbonate minerals. Loss of mass after gravimetry measurement at given temperatures shows that the samples have significant amount of water in their structure (≈3 wt% (120 oC)) with larger weight loss at 600 oC (3.06 and 3.37 wt%) while total weight loss is 9.12 and 9.08 wt% for 1(SC) and 2(SV) respectively. The studied clays from "Slatina" deposit have a medium content of smectite-illite minerals with smaller amount of kaolinite mineral together with quartz and feldspars. Based on their mineral composition and characteristics, possible application should be in different types of ceramic and construction industries. REFERENCES - M. Milošević, M. Logar, B. Dojčinović, A. Rosić and S. Erić, 2016, Diffuse reflectance spectra of methylene blue adsorbed on different types of clay samples, Clay Minerals, (2016) 5, 1-15
Hydrogen and oxygen isotope exchange reactions between clay minerals and water
O'Neil, J.R.; Kharaka, Y.K.
1976-01-01
The extent of hydrogen and oxygen isotope exchange between clay minerals and water has been measured in the temperature range 100-350?? for bomb runs of up to almost 2 years. Hydrogen isotope exchange between water and the clays was demonstrable at 100??. Exchange rates were 3-5 times greater for montmorillonite than for kaolinite or illite and this is attributed to the presence of interlayer water in the montmorillonite structure. Negligible oxygen isotope exchange occurred at these low temperatures. The great disparity in D and O18 exchange rates observed in every experiment demonstrates that hydrogen isotope exchange occurred by a mechanism of proton exchange independent of the slower process of O18 exchange. At 350?? kaolinite reacted to form pyrophyllite and diaspore. This was accompanied by essentially complete D exchange but minor O18 exchange and implies that intact structural units in the pyrophyllite were inherited from the kaolinite precursor. ?? 1976.
Rare earth minerals in a “no tonstein” section of the Dean (Fire Clay) coal, Knox County, Kentucky
DOE Office of Scientific and Technical Information (OSTI.GOV)
Hower, James C.; Berti, Debora; Hochella, Michael F.
The Dean (Fire Clay) coal in Knox County, Kentucky, does not contain the megascopically-visible ash-fall tonstein present in most other sections of the coal bed. Like the Fire Clay tonstein, a low-ash portion of the coal is enriched in rare earth elements (>2400 ppm, on ash basis). In addition to kaolinite produced in the diagenesis of volcanic glass, transmission electron microscopy studies indicate the coal contains primary kaolinite, LaCeNdTh monazite, barium niobate, native gold, and FeNiCr spinels. The mineral assemblages, particularly the kaolinite-monazite association and its similarity to the tonsteins in coal to the east, demonstrate the coal was subjectmore » to the REE-enriched volcanic ash fall, apparently just at a more dilute level than at locations where the tonstein is present.« less
Rare earth minerals in a “no tonstein” section of the Dean (Fire Clay) coal, Knox County, Kentucky
Hower, James C.; Berti, Debora; Hochella, Michael F.; ...
2018-05-03
The Dean (Fire Clay) coal in Knox County, Kentucky, does not contain the megascopically-visible ash-fall tonstein present in most other sections of the coal bed. Like the Fire Clay tonstein, a low-ash portion of the coal is enriched in rare earth elements (>2400 ppm, on ash basis). In addition to kaolinite produced in the diagenesis of volcanic glass, transmission electron microscopy studies indicate the coal contains primary kaolinite, LaCeNdTh monazite, barium niobate, native gold, and FeNiCr spinels. The mineral assemblages, particularly the kaolinite-monazite association and its similarity to the tonsteins in coal to the east, demonstrate the coal was subjectmore » to the REE-enriched volcanic ash fall, apparently just at a more dilute level than at locations where the tonstein is present.« less
Experimental study of Human Adenoviruses interactions with clays
NASA Astrophysics Data System (ADS)
Bellou, Maria; Syngouna, Vasiliki; Paparrodopoulos, Spyros; Vantarakis, Apostolos; Chrysikopoulos, Constantinos
2014-05-01
Clays are used to establish low permeability liners in landfills, sewage lagoons, water retention ponds, golf course ponds, and hazardous waste sites. Human adenoviruses (HAdVs) are waterborne viruses which have been used as viral indicators of fecal pollution. The objective of this study was to investigate the survival of HAdV in static and dynamic clay systems. The clays used as a model were crystalline aluminosilicates: kaolinite and bentonite. The adsorption and survival of HAdVs onto these clays were characterized at two different controlled temperatures (4 and 25o C) under static and dynamic batch conditions. Control tubes, in the absence of clay, were used to monitor virus inactivation due to factors other than adsorption to clays (e.g. inactivation or sorption onto the tubes walls). For both static and dynamic batch experiments, samples were collected for a maximum period of seven days. This seven day time - period was determined to be sufficient for the virus-clay systems to reach equilibrium. To infer the presence of infectious HAdV particles, all samples were treated with Dnase and the extraction of viral nucleid acid was performed using a commercial viral RNA kit. All samples were analyzed by Real - Time PCR which was used to quantify viral particles in clays. Samples were also tested for virus infectivity by A549 cell cultures. Exposure time intervals in the range of seven days (0.50-144 hours) resulted in a load reduction of 0.74 to 2.96 logs for kaolinite and a reduction of 0.89 to 2.92 for bentonite. Furthermore, virus survival was higher onto bentonite than kaolinite (p
The Weathering of Rocks Under Humid Tropical Conditions.
kaolinitic clay, the formation of gibbsite from the kaolinite , and the leaching of silica and iron-oxides. (Modified author abstract)...rhyolitic to andesitic lavas, tuffs and granophyre, under warm humid climatic conditions. The dominant minerals in the bauxite deposits are gibbsite ... kaolinite , quartz (also chalcedony), goethite, and hematite. The occurrence of bauxite is determined primarily by the parent rocks, which are typically fine
Biodegradation of crude oil saturated fraction supported on clays.
Ugochukwu, Uzochukwu C; Jones, Martin D; Head, Ian M; Manning, David A C; Fialips, Claire I
2014-02-01
The role of clay minerals in crude oil saturated hydrocarbon removal during biodegradation was investigated in aqueous clay/saturated hydrocarbon microcosm experiments with a hydrocarbon degrading microorganism community. The clay minerals used for this study were montmorillonite, palygorskite, saponite and kaolinite. The clay mineral samples were treated with hydrochloric acid and didecyldimethylammonium bromide to produce acid activated- and organoclays respectively which were used in this study. The production of organoclay was restricted to only montmorillonite and saponite because of their relative high CEC. The study indicated that acid activated clays, organoclays and unmodified kaolinite, were inhibitory to biodegradation of the hydrocarbon saturates. Unmodified saponite was neutral to biodegradation of the hydrocarbon saturates. However, unmodified palygorskite and montmorillonite were stimulatory to biodegradation of the hydrocarbon saturated fraction and appears to do so as a result of the clays' ability to provide high surface area for the accumulation of microbes and nutrients such that the nutrients were within the 'vicinity' of the microbes. Adsorption of the saturated hydrocarbons was not significant during biodegradation.
Effect of Dissolved NaC1 on Freezing Curves of Kaolinite, Montmorillonite, and Sand Pastes,
1999-01-01
test this procedure. Pastes of kaolinite clay, montmorillonite , and quartz sand were prepared by washing repeatedly with aque- ous solutions of 0.1...Cold Regions Research & Engineering Laboratory Effect of Dissolved NaCI on Freezing Curves of Kaolinite , Montmorillonite , and Sand Pastes S.A...of kaolinite pastes warmed from -66.6°C to 0°C 8 4. Unfrozen-water contents, as measured by pulsed NMR, of montmorillonite pastes cooled from 0
Moyo, Francis; Tandlich, Roman; Wilhelmi, Brendan S.; Balaz, Stefan
2014-01-01
Renewed focus on the sorption of hydrophobic organic chemicals (HOCs) onto mineral surfaces and soil components is required due to the increased and wider range of organic pollutants being released into the environment. This mini-review examines the possibility of the contribution and mechanism of HOC sorption onto clay mineral sorbents such as kaolinite, and soil organic matter and the possible role of both in the prevention of environmental contamination by HOCs. Literature data indicates that certain siloxane surfaces can be hydrophobic. Therefore soils can retain HOCs even at low soil organic levels and the extent will depend on the structure of the pollutant and the type and concentration of clay minerals in the sorbent. Clay minerals are wettable by nonpolar solvents and so sorption of HOCs onto them from aqueous and non-aqueous solutions is possible. This is important for two reasons: firstly, the movement and remediation of soil environments will be a function of the concentration and type of clay minerals in the soil. Secondly, low-cost sorbents such as kaolinite and expandable clays can be added to soils or contaminated environments as temporary retention barriers for HOCs. Inorganic cations sorbed onto the kaolinite have a strong influence on the rate and extent of sorption of hydrophobic organic pollutants onto kaolinite. Structural sorbate classes that can be retained by the kaolinite matrix are limited by hydrogen bonding between hydroxyl groups of the octahedral alumosilicate sheet and the tetrahedral sheet with silicon. Soil organic carbon plays a key role in the sorption of HOCs onto soils, but the extent will be strongly affected by the structure of the organic soil matter and the presence of soot. Structural characterisation of soil organic matter in a particular soil should be conducted during a particular contamination event. Contamination by mining extractants and antibiotics will require renewed focus on the use of the QSAR approaches in the context of the sorption of HOCs onto clay minerals from aqueous and non-aqueous solutions. PMID:24821385
Geology and resources of the Andersonville, Georgia, kaolin and bauxite district
Cofer, Harland E.; Manker, John Phillip
1983-01-01
The kaolin and kaolin-rich sediments of the Andersonville district were deposited in an estuary environment with restricted circulation and little tidal or longshore current influence. Micaceous kaolinitic clays were deposited during late Paleocene time on broad, shallow water flats between deeper water distributary channels in the estuarine system. During the cycle of deposition, kaolinitic sediments were temporarily exposed to weathering leading to bauxitization and further kaolinization. Subsequently, subaerial and/or subaqueous erosion planed off and redeposited some of the weathering products as organic-rich clays and silts, berthierine-bearing clays, and rarely as colluvial bauxite and sedimentary bauxitic clays. Upon resubmergence, gibbsite-rich, porous bauxite, and bauxitic clays were exposed to silica-saturated water of the estuary. Gibbsite reacted with silica to form kaolinite and resulted in the formation of the transitional (bauxitic) clays overlying the bauxite. Kaolinitic sediments transported by streams again spread over the altered and redeposited material. At the close of the kaolin depositional period movement along the Andersonville Fault Zone and related faults changed the basinal configuration, and the area of the uplifted (southern) block of the fault was exposed to weathering and bauxitization for a limited period of time. General submergence again occurred and much of the district was covered by marine and brackish water, ending the period of commercial kaolin deposition. The kaolin and bauxite deposits in the Andersonville district form a broad belt 15 kilometers wide and 22 kilometers long trending in a northwest-southeastward direction. Most of the kaolin and bauxite of commercial value occur within a narrow 10-kilometer-wide zone in the belt. The reserves of kaolin suitable for refractory and chemical use are approximately 290 million tonnes. Paramarginal resources of sandy kaolin suitable for refractory, chemical, or aluminum manufacture after beneficiation are approximately 240 million tonnes. Indicated and inferred reserves of bauxite and bauxitic clay are 1.8 million tonnes and 7.3 million tonnes respectively.
21 CFR 186.1256 - Clay (kaolin).
Code of Federal Regulations, 2012 CFR
2012-04-01
... CONSUMPTION (CONTINUED) INDIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific...-58-7) consists of hydrated aluminum silicate. The commercial products of clay (kaolin) contain... kaolin. Kaolinite or china clay is whiter, less contaminated with extraneous minerals, and less plastic...
21 CFR 186.1256 - Clay (kaolin).
Code of Federal Regulations, 2011 CFR
2011-04-01
... CONSUMPTION (CONTINUED) INDIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific...-58-7) consists of hydrated aluminum silicate. The commercial products of clay (kaolin) contain... kaolin. Kaolinite or china clay is whiter, less contaminated with extraneous minerals, and less plastic...
21 CFR 186.1256 - Clay (kaolin).
Code of Federal Regulations, 2013 CFR
2013-04-01
... CONSUMPTION (CONTINUED) INDIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific...-58-7) consists of hydrated aluminum silicate. The commercial products of clay (kaolin) contain... kaolin. Kaolinite or china clay is whiter, less contaminated with extraneous minerals, and less plastic...
21 CFR 186.1256 - Clay (kaolin).
Code of Federal Regulations, 2010 CFR
2010-04-01
... CONSUMPTION (CONTINUED) INDIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific...-58-7) consists of hydrated aluminum silicate. The commercial products of clay (kaolin) contain... kaolin. Kaolinite or china clay is whiter, less contaminated with extraneous minerals, and less plastic...
Weck, Philippe F.; Kim, Eunja; Jove-Colon, Carlos F.
2015-03-04
In this study, the structural, mechanical and thermodynamic properties of 1 : 1 layered dioctahedral kaolinite clay, with ideal Al 2Si 2O 5(OH) 4 stoichiometry, were investigated using density functional theory corrected for dispersion interactions (DFT-D2). The bulk moduli of 56.2 and 56.0 GPa predicted at 298 K using the Vinet and Birch–Murnaghan equations of state, respectively, are in good agreement with the recent experimental value of 59.7 GPa reported for well-crystallized samples. The isobaric heat capacity computed for uniaxial deformation of kaolinite along the stacking direction reproduces calorimetric data within 0.7–3.0% from room temperature up to its thermal stabilitymore » limit.« less
Phosphates in some Missouri refractory clays
Halley, Robert B.; Foord, Eugene E.; Keller, David J.; Keller, Walter D.
1997-01-01
This paper describes in detail phosphate minerals occurring in refractory clays of Missouri and their effect on the refractory degree of the clays. The minerals identified include carbonate-fluorapatite (francolite), crandallite, goyazite, wavellite, variscite and strengite. It is emphasized that these phosphates occur only in local isolated concentrations, and not generally in Missouri refractory clays.The Missouri fireclay region comprises 2 districts, northern and southern, separated by the Missouri River. In this region, clay constitutes a major part of the Lower Pennsylvanian Cheltenham Formation. The original Cheltenham mud was an argillic residue derived from leaching and dissolution of pre-Pennsylvanian carbonates. The mud accumulated on a karstic erosion surface truncating the pre-Cheltenham rocks. Fireclays of the northern district consist mainly of poorly ordered kaolinite, with variable but minor amounts of illite, chlorite and fine-grained detrital quartz. Clays of the southern district were subjected to extreme leaching that produced well-ordered kaolinite flint clays. Local desilication formed pockets of diaspore, or more commonly, kaolinite, with oolite-like nubs or burls of diaspore (“burley”" clay).The phosphate-bearing materials have been studied by X-ray diffraction (XRD), scanning electron microscopy-energy dispersive spectral analysis (SEM-EDS) and chemical analysis. Calcian goyazite was identified in a sample of diaspore, and francolite in a sample of flint clay. A veinlet of wavellite occurs in flint clay at one locality, and a veinlet of variscite-strengite at another locality.The Missouri flint-clay-hosted francolite could not have formed in the same manner as marine francolite. The evidence suggests that the Cheltenham francolite precipitated from ion complexes in pore water, nearly simultaneously with crystallization of kaolinite flint clay from an alumina-silica gel. Calcian goyazite is an early diagenetic addition to its diaspore host. The wavellite and variscite-strengite veinlets are secondary, precipitated from ion complexes in ground water percolating along cracks in the flint clay. The flint clay host of the variscite-strengite veinlet contains strontian crandallite. All of the phosphates contain significant amounts of strontium. The source of P, Ca and Sr was the marine carbonates. Dissolution of these carbonates produced the argillic residue that became the primordial Cheltenham paludal mud, which ultimately altered to fireclay.Preliminary firing tests show that the presence of phosphates lowers fusion temperature. However, it is not clear whether poor refractoriness is due to the presence of phosphates, per se, or to Ca, Sr and other alkaline elements present in the phosphates.
Interface Modeling for Electro-Osmosis in Subgrade Structures
2004-12-01
aggregate and different clays ( kaolinite , montmorillonite , limestone and quartz sands) created to simulate below grade structures. A direct current 30...Quartz Sand 100 Sieve Ca Montmorillonite Na Montmorillonite Kaolinite The test setup used a 0.45 water to cement ratio concrete cylinder... Kaolinite cell Figure 4. Measured pH for Concrete and Na Montmorillonite cell 4 Scaling occurred at the interface between the anode
Effects of simulated clay gouges on the sliding behavior of Tennessee sandston
NASA Astrophysics Data System (ADS)
Shimamoto, Toshihiko; Logan, John M.
1981-06-01
The effects of simulated fault gouge on the sliding behavior of Tennessee sandstone are studied experimentally with special reference to the stabilizing effect of clay minerals mixed into the gouge. About 30 specimens with gouge composed of pure clays, of homogeneously mixed clay and anhydrite, or of layered clay and anhydrite, along a 35° precut are deformed dry in a triaxial apparatus at a confining pressure of 100 MPa, with a shortening rate of about 5 · 10 -4/sec, and at room temperature. Pure clay gouges exhibit only stable sliding, and the ultimate frictional strength is very low for bentonite (mont-morillonite), intermediate for chlorite and illite, and considerably higher for kaolinite. Anhydrite gouge shows violent stick-slip at 100 MPa confining pressure. When this mineral is mixed homogeneously with clays, the frictional coefficient of the mixed gouge, determined at its ultimate frictional strength, decreases monotonically with an increase in the clay content. The sliding mode changes from stick-slip to stable sliding when the frictional coefficient of the mixed clay-anhydrite gouge is lowered down below 90-95% of the coefficient of anhydrite gouge. The stabilizing effect of clay in mixed gouge is closely related to the ultimate frictional strength of pure clays; that is, the effect is conspicuous only for a mineral with low frictional strength. Only 15-20% of bentonite suppresses the violent stick-slip of anhydrite gouge. In contrast, violent stick-slip occurs even if the gouge contains as much as 75% of kaolinite. The behavior of illite and chlorite is intermediate between that of kaolinite and bentonite. Bentonite—anhydrite two-layer gouge exhibits stable sliding even when the bentonite content is only 5%. Thus, the presence of a thin, clay-rich layer in a fault zone stabilizes the behavior much more effectively than do the clay minerals mixed homogeneously with the gouge. This result brings out the mechanical significance of internal structures of a fault zone in understanding the effects of intrafault materials on the fault motion. Based on the present experimental results incorporated with some other experimental data, it is argued that although the stabilizing effect of montmorillonite and vermiculite is indeed remarkable at room temperature, the effect should be much less pronounced at elevated temperatures, due perhaps to the dewatering of the clays. In most geological environments where shallow earthquakes occur, the stabilizing effect of clays is probably not so conspicuous as to completely suppress the unstable motion of a fault.
New organophilic kaolin clays based on single-point grafted 3-aminopropyl dimethylethoxysilane.
Zaharia, A; Perrin, F-X; Teodorescu, M; Radu, A-L; Iordache, T-V; Florea, A-M; Donescu, D; Sarbu, A
2015-10-14
In this study, the organophilization procedure of kaolin rocks with a monofunctional ethoxysilane- 3 aminopropyl dimethyl ethoxysilane (APMS) is depicted for the first time. The two-step organophilization procedure, including dimethyl sulfoxide intercalation and APMS grafting onto the inner hydroxyl surface of kaolinite (the mineral) layers was tested for three sources of kaolin rocks (KR, KC and KD) with various morphologies and kaolinite compositions. The load of APMS in the kaolinite interlayer space was higher than that of 3-aminopropyl triethoxysilane (APTS) due to the single-point grafting nature of the organophilization reaction. A higher long-distance order of kaolinite layers with low staking was obtained for the APMS, due to a more controllable organiphilization reaction. Last but not least, the solid state (29)Si-NMR tests confirmed the single-point grafting mechanism of APMS, corroborating monodentate fixation on the kaolinite hydroxyl facets, with no contribution to the bidentate or tridentate fixation as observed for APTS.
Lavie, S; Stotzky, G
1986-01-01
The respiration of three phenotypes of Histoplasma capsulatum, the causal agent of histoplasmosis in humans, was markedly reduced by low concentrations of montmorillonite but was reduced less by even higher concentrations of kaolinite or attapulgite (palygorskite). The reduction in respiration followed a pattern that suggested saturation-type kinetics: an initial sharp reduction that occurred with low concentrations of clay (0.01 to 0.5% [wt/vol]), followed by a more gradual reduction with higher concentrations (1 to 8%). Increases in viscosity (which could impair the movement of O2) caused by the clays were not responsible for the reduction in respiration, and the clays did not interfere with the availability of nutrients. Scanning electron microscopy after extensive washing showed that the clay particles were tightly bound to the hyphae, suggesting that the clays reduced the rate of respiration of H. capsulatum by adhering to the mycelial surface and, thereby, interfered with the movement of nutrients, metabolites, and gases across the mycelial wall. Images PMID:3954340
Lavie, S; Stotzky, G
1986-01-01
The respiration of three phenotypes of Histoplasma capsulatum, the causal agent of histoplasmosis in humans, was markedly reduced by low concentrations of montmorillonite but was reduced less by even higher concentrations of kaolinite or attapulgite (palygorskite). The reduction in respiration followed a pattern that suggested saturation-type kinetics: an initial sharp reduction that occurred with low concentrations of clay (0.01 to 0.5% [wt/vol]), followed by a more gradual reduction with higher concentrations (1 to 8%). Increases in viscosity (which could impair the movement of O2) caused by the clays were not responsible for the reduction in respiration, and the clays did not interfere with the availability of nutrients. Scanning electron microscopy after extensive washing showed that the clay particles were tightly bound to the hyphae, suggesting that the clays reduced the rate of respiration of H. capsulatum by adhering to the mycelial surface and, thereby, interfered with the movement of nutrients, metabolites, and gases across the mycelial wall.
Carbonation of Clay Minerals Exposed to scCO2/Water at 200 degrees and 250 degrees C
DOE Office of Scientific and Technical Information (OSTI.GOV)
Sugama, T.; Ecker, L.; Gill, S.
2010-11-01
To clarify the mechanisms of carbonation of clay minerals, such as bentonite, kaolinite, and soft clay, we exposed them to supercritical carbon dioxide (scCO2)/water at temperatures of 200 and 250 C and pressures of 1500 and 2000 psi for 72- and 107-hours. Bentonite, comprising three crystalline phases, montmorillonite (MMT), anorthoclase-type albite, and quartz was susceptible to reactions with ionic carbonic acid yielded by the interactions between scCO2 and water, particularly MMT and anorthoclase-type albite phases. For MMT, the cation-exchangeable ions, such as Na+ and Ca2+, present in its basal interplanar space, were replaced by proton, H+, from ionic carbonic acid;more » thereafter, the cations leaching from MMT directly reacted with CO32- as a counter ion of H+ to form carbonate compounds. Such in-situ carbonation process in basal space caused the shrinkage and breakage of the spacing structure within MMT. In contrast, the wet carbonation of anorthoclase-type albite, categorized as rock minerals, entailed the formation of three amorphous by-products, such as carbonates, kaolinite-like compounds, and silicon dioxide. Together, these two different carbonations caused the disintegration and corruption of bentonite. Kaolinite clay containing the amorphous carbonates and silicon dioxide was inert to wet carbonation. We noted only a gain in weight due to its water uptake, suggesting that kaolinite-like by-products generated by the wet carbonation of rock minerals might remain unchanged even during extended exposure. Soft clay consisting of two crystalline phases, dolomite and silicon dioxide, also was unaltered by wet carbonation, despite the uptake of water.« less
Kang, Fuxing; Ge, Yangyang; Hu, Xiaojie; Goikavi, Caspar; Waigi, Michael Gatheru; Gao, Yanzheng; Ling, Wanting
2016-12-15
In current adsorption studies of biotoxins to phyllosilicate clays, multiply weak bonding types regarding these adsorptions are not well known; the major attractive forces, especially for kaolinite and illite, are difficult to be identified as compared to smectite with exchangeable cations. Here, we discriminated the bonding types of aflatoxin B1 (AFB1) contaminant to these clays by combined batch experiment with model computation, expounded their bonding mechanisms which have been not quantitatively described by researchers. The observed adsorbent-to-solution distribution coefficients (K d ) of AFB1 presented in increasing order of 18.5-37.1, 141.6-158.3, and 354.6-484.7L/kg for kaolinite, illite, and smectite, respectively. Normalization of adsorbent-specific surface areas showed that adsorption affinity of AFB1 is mainly dependent on the outside surfaces of clay aggregates. The model computation and test of ionic effect further suggested that weakly electrostatic attractions ((Si/Al-OH) 2 ⋯(OC) 2 ) are responsible for AFB1-kaolinite adsorption (K d , 18.5-37.1L/kg); a moderate electron-donor-acceptor attraction ((CO) 2 ⋯K + ⋯(O-Al) 3 ) is related to AFB1-illite adsorption (K d , 141.6-158.3L/kg); a strong calcium-bridging linkage ((CO) 2 ⋯Ca 2+ ⋯(O-Si) 4 ) is involved in AFB1-smectite adsorption (K d , 354.6-484.7L/kg). Changes in Gibbs free energy (ΔG°) suggested that the computed result is reliable, providing a good reproduction of AFB1-clay interaction. Copyright © 2016 Elsevier B.V. All rights reserved.
Clay minerals behaviour in thin sandy clay-rich lacustrine turbidites (Lake Hazar, Turkey)
NASA Astrophysics Data System (ADS)
El Ouahabi, Meriam; Hubert-Ferrari, Aurelia; Lamair, Laura; Hage, Sophie
2017-04-01
Turbidites have been extensively studied in many different areas using cores or outcrop, which represent only an integrated snapshot of a dynamic evolving flow. Laboratory experiments provide the missing relationships between the flow characteristics and their deposits. In particular, flume experiments emphasize that the presence of clay plays a key role in turbidity current dynamics. Clay fraction, in small amount, provides cohesive strength to sediment mixtures and can damp turbulence. However, the degree of flocculation is dependent on factors such as the amount and size of clay particles, the surface of clay particles, chemistry and pH conditions in which the clay particles are dispersed. The present study focuses on thin clayey sand turbidites found in Lake Hazar (Turkey) occurring in stacked thin beds. Depositional processes and sources have been previously studied and three types were deciphered, including laminar flows dominated by cohesion, transitional, and turbulence flow regimes (Hage et al., in revision). For the purpose of determine the clay behavior in the three flow regimes, clay mineralogical, geochemical measurements on the cores allow characterising the turbidites. SEM observations provide further information regarding the morphology of clay minerals and other clasts. The study is particularly relevant given the highly alkaline and saline water of the Hazar Lake. Clay minerals in Hazar Lake sediments include kaolinite (1:1-type), illite and chlorite (2:1-type). Hazar lake water is alkaline having pH around 9.3, in such alkaline environment, a cation-exchange reaction takes place. Furthermore, in saline water (16‰), salts can act as a shield and decrease the repulsive forces between clay particle surfaces. So, pH and salt content jointly impact the behaviour of clays differently. Since the Al-faces of clay structures have a negative charge in basic solutions. At high pH, all kaolinite surfaces become negative-charged, and then kaolinite particles are dispersed, and the suspension is stabilized supported by our SEM observations. In alkaline water, kaolinite reveals a lower degree of consolidation. While, alkaline water has no measurable effect on illite and chlorite surface properties due to the absence of modifications in charge. Illite and chlorite form with other clasts clusters or aggregate structures in suspension when the particle interactions are dominated by attractive energies were formed. The aggregate structure plays a major part in the flow behavior of clay suspensions. Flocs will immobilize the suspending medium, and give rise to increasing viscosity and yield strength of the suspension. S. Hage, A. Hubert-Ferrari, L. Lamair, U. Avşar, M. El Ouahabi, M. Van Daele, F. Boulvain, M.A. Bahri, A. Seret, Al. Plenevaux. Flow dynamics at the origin of thin sandy clay-rich lacustrine turbidites: Examples from Lake Hazar, Turkey, submitted to Sedimentology, in revision.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Ohnuki, T.; Francis, A.; Kozai, N.
2010-04-01
We conducted a series of basic studies on the microbial accumulation of actinides to elucidate their migration behavior around backfill materials used in the geological disposal of radioactive wastes. We explored the interactions of U(VI) and Pu(VI) with Bacillus subtilis, kaolinite clay, and within a mixture of the two, directly analyzing their association with the bacterium in the mixture by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The accumulation of U by the mixture rose as the numbers of B. subtilis cells increased. Treating the kaolinite with potassium acetate (CH{sub 3}COOK) removed approximately 80% of the associated uraniummore » while only 65% was removed in the presence of B. subtilis. TEM-EDS analysis confirmed that most of the U taken from solution was associated with B. subtilis. XANES analyses revealed that the oxidation state of uranium associated with B. subtilis, kaolinite, and with the mixture containing both was U(VI). The amount of Pu sorbed by B. subtilis increased with time, but did not reach equilibrium in 48 h; in kaolinite alone, equilibrium was attained within 8 h. After 48 h, the oxidation state of Pu in the solutions exposed to B. subtilis and to the mixture had changed to Pu(V), whereas the oxidation state of the Pu associated with both was Pu(IV). In contrast, there was no change in the oxidation state of Pu in the solution nor on kaolinite after exposure to Pu(VI). SEM-EDS analysis indicated that most of the Pu in the mixture was associated with the bacteria. These results suggest that U(VI) and Pu(VI) preferentially are sorbed to bacterial cells in the presence of kaolinite clay, and that the mechanism of accumulation of U and Pu differs. U(VI) is sorbed directly to the bacterial cells, whereas Pu(VI) first is reduced to Pu(V) and then to Pu(IV), and the latter is associated with the cells. These results have important implications on the migrations of radionuclides around the repository sites of geological disposal. Microbial cells compete with clay colloids for radionuclides accumulation, and because of their higher affinity and larger size, the microbes accumulate radionuclides and migrate much slower than do the clay colloids. Additionally, biofilm coatings formed on the fractured rock surfaces also accumulate radionuclides, thereby retarding radionuclide migration.« less
Influence of Compositional Variations on Floc Size and Strength
NASA Astrophysics Data System (ADS)
Yin, H.; Tan, X.; Reed, A. H.; Furukawa, Y.; Zhang, G.
2010-12-01
Clay-biopolymer micro aggregates or flocs are abundant in waters, including rivers, lakes, and oceans. Owing to their small size and charged surfaces, fine-grained inorganic sediment particles, mainly clays, interact actively with organic substances, such as organic matter and biogenic polymers, to form aggregates or flocs, typically in the size of 10-1000 μm. The flocs in ocean waters are also termed “marine snow”. These flocs are typically porous, tenuous, and soft in nature. During transport in suspension, they may breakdown and decrease in size if the turbulent shear stress exceeds their strength. They may also collide and form larger ones if the shear stress is relatively small. Since flocs of different size and structure settle at different velocities, understanding their strength is also of essential importance for sediment hydrodynamics, transport, and management. Our study focuses on investigating the influence of compositional variations on floc size and strength so that a better understanding of floc dynamics can be achieved. A laser diffraction-based Cilas® particle size and shape analyzer with controllable fluid circulation velocity was employed to conduct floc size measurements and shape imaging, the latter achieved by a high resolution inverted optical microscope, which is also installed with the size analyzer. Totally two clay minerals, kaolinite and illite, were tested as the model inorganic solid skeleton minerals for floc formation, and two biopolymers, anionic xanthan gum and neutral guar gum, were chosen as analogs of naturally occurring organic matter or biopolymers to simulate clay-biopolymer floc formation. Moreover, the concentration of both organic and inorganic phases was varied. The floc breakage or tensile strength was indirectly estimated by the varied fluid flow velocity in the particle size analyzer’s circulation system. For each individual composition, stable flocs were formed by three different fluid circulating velocities, resulting in different shearing stress in the fluid. Experimental results show that organic biopolymers can have profound influences on clay flocculation process and the resultant floc size and strength. Anionic xanthan gum tends to form smaller and weaker clay-biopolymer flocs than neutral guar gum, because the Coulombic repulsion forces develop between the two negatively charged constituents. Illite results in stronger clay-guar flocs than kaolinite, probably due to the relatively higher negative charges on illite surface. Generally, a bimodal distribution of floc size frequency was observed for all types of flocs. The maxim floc sizes range from 10-30 μm for kaolinite-xanthan flocs to 250-300 μm for kaolinite-guar flocs at a weight ratio of 1:1.
1981-12-01
plagio - clase feldspar and pyroxene. The tine fraction may Surface area and its effects contain the clay "sheet" minerals (i.e. kaolinite. illite...Pyroxene, Kaoliniwe Unified By By Ortho. Plagio . amphibole, Basic clay min. Hematite Soil Soil soil petrogr. X.ray clase clase and Igneous and clay and no
NASA Astrophysics Data System (ADS)
Zhang, Bin; Kang, Jianting; Kang, Tianhe
2018-05-01
CH4 adsorption isotherms of kaolinite with moisture contents ranging from 0 to 5 wt% water, the effects of water on maximum adsorption capacity, kaolinite swelling, and radial distribution function were modelled by the implementing combined Monte Carlo (MC) and molecular dynamics (MD) simulations at 293.15 K (20 °C) and a pressure range of 1-20 MPa. The simulation results showed that the absolute adsorption of CH4 on both dry and moist kaolinite followed a Langmuir isotherm within the simulated pressure range, and both the adsorption capacity and the rate of CH4 adsorption decreased with the water content increases. The adsorption isosteric heats of CH4 on kaolinite decreased linearly with increasing water content, indicating that at higher water contents, the interaction energy between the CH4 and kaolinite was weaker. The interaction between kaolinite and water dominates and was the main contributing factor to kaolinite clay swelling. Water molecules were preferentially adsorbed onto oxygen and hydrogen atoms in kaolinite, while methane showed a tendency to be adsorbed only onto oxygen. The simulation results of our study provide the quantitative analysis of effect of water on CH4 adsorption capacity, adsorption rate, and interaction energy from a microscopic perspective. We hope that our study will contribute to the development of strategies for the further exploration of coal bed methane and shale gas.
Effects of clay minerals on transport of graphene oxide in saturated porous media.
Lu, Taotao; Xia, Tianjiao; Qi, Yu; Zhang, Chengdong; Chen, Wei
2017-03-01
The presence of kaolinite, montmorillonite, and illite in packed quartz sand inhibited the transport of graphene oxide to different degrees. Transport inhibition was exerted mainly by the presence of positively charged sites on clay edges (which served as favorable deposition sites), whereas the effects on the overall particle-collector interaction energy and flow path were small. Kaolinite exhibited the most significant transport-inhibition effects because of its high percentage of edge area. Environ Toxicol Chem 2017;36:655-660. © 2016 SETAC. © 2016 SETAC.
Clay-mineral suites, sources, and inferred dispersal routes: Southern California continental shelf
Hein, J.R.; Dowling, J.S.; Schuetze, A.; Lee, H.J.
2003-01-01
Clay mineralogy is useful in determining the distribution, sources, and dispersal routes of fine-grained sediments. In addition, clay minerals, especially smectite, may control the degree to which contaminants are adsorbed by the sediment. We analyzed 250 shelf sediment samples, 24 river-suspended-sediment samples, and 12 river-bed samples for clay-mineral contents in the Southern California Borderland from Point Conception to the Mexico border. In addition, six samples were analyzed from the Palos Verdes Headland in order to characterize the clay minerals contributed to the offshore from that point source. The <2 ??m-size fraction was isolated, Mg-saturated, and glycolated before analysis by X-ray diffraction. Semi-quantitative percentages of smectite, illite, and kaolinite plus chlorite were calculated using peak areas and standard weighting factors. Most fine-grained sediment is supplied to the shelf by rivers during major winter storms, especially during El Nin??o years. The largest sediment fluxes to the region are from the Santa Ynez and Santa Clara Rivers, which drain the Transverse Ranges. The mean clay-mineral suite for the entire shelf sediment data set (26% smectite, 50% illite, 24% kaolinite+chlorite) is closely comparable to that for the mean of all the rivers (31% smectite, 49% illite, 20% kaolinite+chlorite), indicating that the main source of shelf fine-grained sediments is the adjacent rivers. However, regional variations do exist and the shelf is divided into four provinces with characteristic clay-mineral suites. The means of the clay-mineral suites of the two southernmost provinces are within analytical error of the mineral suites of adjacent rivers. The next province to the north includes Santa Monica Bay and has a suite of clay minerals derived from mixing of fine-grained sediments from several sources, both from the north and south. The northernmost province clay-mineral suite matches moderately well that of the adjacent rivers, but does indicate some mixing from sources in adjacent provinces.
Wang, Miao-miao; Sun, Zhi-gao; Lu, Xiao-ning; Wang, Wei; Wang, Chuan-yuan
2015-04-01
Based on the laser particle size and X-ray diffraction (XRD) analysis, 28 sediment samples collected from the inshore region of the Yellow River estuary in October 2013 were determined to discuss the influence of long-term implementation of the flow-sediment regulation scheme (FSRS, initiated in 2002) on the distributions of grain size and clay components (smectite, illite, kaolinite and chlorite) in sediments. Results showed that, after the FSRS was implemented for more than 10 years, although the proportion of sand in inshore sediments of the Yellow River estuary was higher (average value, 23.5%) than those in sediments of the Bohai Sea and the Yellow River, silt was predominated (average value, 59.1%) and clay components were relatively low (average value, 17.4%). The clay components in sediments of the inshore region in the Yellow River estuary were close with those in the Yellow River. The situation was greatly changed due to the implementation of FSRS since 2002, and the clay components were in the order of illite > smectite > chlorite > kaolinite. This study also indicated that, compared to large-scale investigation in Bohai Sea, the local study on the inshore region of the Yellow River estuary was more favorable for revealing the effects of long-term implementation of the FSRS on sedimentation environment of the Yellow River estuary.
NASA Astrophysics Data System (ADS)
Chenot, Elise; Deconinck, Jean-François; Pucéat, Emmanuelle; Pellenard, Pierre; Guiraud, Michel; Jaubert, Maxime; Jarvis, Ian; Thibault, Nicolas; Cocquerez, Théophile; Bruneau, Ludovic; Razmjooei, Mohammad J.; Boussaha, Myriam; Richard, James; Sizun, Jean-Pierre; Stemmerik, Lars
2018-03-01
New clay mineralogical analyses have been performed on Campanian sediments from the Tethyan and Boreal realms along a palaeolatitudinal transect from 45° to 20°N (Danish Basin, North Sea, Paris Basin, Mons Basin, Aquitaine Basin, Umbria-Marche Basin and Tunisian Atlas). Significant terrigenous inputs are evidenced by increasing proportions of detrital clay minerals such as illite, kaolinite and chlorite at various levels in the mid- to upper Campanian, while smectitic minerals predominate and represented the background of the Late Cretaceous clay sedimentation. Our new results highlight a distinct latitudinal distribution of clay minerals, with the occurrence of kaolinite in southern sections and an almost total absence of this mineral in northern areas. This latitudinal trend points to an at least partial climatic control on clay mineral sedimentation, with a humid zone developed between 20° and 35°N. The association and co-evolution of illite, chlorite and kaolinite in most sections suggest a reworking of these minerals from basement rocks weathered by hydrolysis, which we link to the formation of relief around the Tethys due to compression associated with incipient Tethyan closure. Diachronism in the occurrence of detrital minerals between sections, with detrital input starting earlier during the Santonian in the south than in the north, highlights the northward progression of the deformation related to the anticlockwise rotation of Africa. Increasing continental weathering and erosion, evidenced by our clay mineralogical data through the Campanian, may have resulted in enhanced CO2 consumption by silicate weathering, thereby contributing to Late Cretaceous climatic cooling.
Guerra, Denis L; Leidens, Victor L; Viana, Rúbia R; Airoldi, Claudio
2010-08-15
The compound N-[3-(trimethoxysilyl)propyl]diethylenetriamine (MPDET) was anchored onto Amazon kaolinite surface (KLT) by heterogeneous route. The modified and natural kaolinite clay samples were characterized by transmission electron microscopy (TEM), scanning electron microscopic (SEM), N(2) adsorption, powder X-ray diffraction, thermal analysis, ion exchange capacities, and nuclear magnetic nuclei of (29)Si and (13)C. The well-defined peaks obtained in the (13)C NMR spectrum in the 5.0-62.1 ppm region confirmed the attachment of organic functional groups as pendant chains bonded into the porous clay. The adsorption of uranyl on natural (KLT) and modified (KLT(MPDET)) kaolinite clays was investigated as a function of the solution pH, metal concentration, temperature, and ionic strength. The ability of these materials to remove U(VI) from aqueous solution was followed by a series of adsorption isotherms adjusted to a Sips equation at room temperature and pH 4.0. The maximum number of moles adsorbed was determined to be 8.37 x 10(-3) and 13.87 x 10(-3) mmol g(-1) for KLT and KLT(MPDET) at 298 K, respectively. The energetic effects (Delta(int)H, Delta(int)G, and Delta(int)S) caused by metal cations adsorption were determined through calorimetric titrations. Copyright 2010. Published by Elsevier B.V.
Lipson, S M; Stotzky, G
1983-01-01
The adsorption of reovirus to clay minerals has been reported by several investigators, but the mechanisms defining this association have been studied only minimally. The purpose of this investigation was to elucidate the mechanisms involved with this interaction. More reovirus type 3 was adsorbed, in both distilled and synthetic estuarine water, by low concentrations of montmorillonite than by comparable concentrations of kaolinite containing a mixed complement of cations on the exchange complex. Adsorption to the clays was essentially immediate and was correlated with the cation-exchange capacity of the clays, indicating that adsorption was primarily to negatively charged sites on the clays. Adsorption was greater with low concentrations of clays in estuarine water than in distilled water, as the higher ionic strength of the estuarine water reduced the electrokinetic potential of both clay and virus particles. The addition of cations (as chloride salts) to distilled water enhanced adsorption, with divalent cations being more effective than monovalent cations and 10(-2) M resulting in more adsorption than 10(-3) M. Potassium ions suppressed reovirus adsorption to montmorillonite, probably by collapsing the clay lattices and preventing the expression of the interlayer-derived cation-exchange capacity. More virus was adsorbed by montmorillonite made homoionic to various mono-, di-, and trivalent cations (except by montmorillonite homoionic to potassium) than by comparable concentrations of kaolinite homoionic to the same cations. The sequence of the amount of adsorption to homoionic montmorillonite was Al greater than Ca greater than Mg greater than Na greater than K; the sequence of adsorption to kaolinite was Na greater than Al greater than Ca greater than Mg greater than K. The constant partition-type adsorption isotherms obtained when the clay concentration was maintained constant and the virus concentration was varied indicated that a fixed proportion of the added virus population was adsorbed, regardless of the concentration of infectious particles. A heterogeneity within the reovirus population was indicated. PMID:6639022
NASA Astrophysics Data System (ADS)
Landrou, Gnanli; Brumaud, Coralie; Habert, Guillaume
2017-06-01
In the ceramic industry and in many sectors, clay minerals are widely used. In earthen construction technique, clay plays a crucial role in the processing. The purpose of this research is to understand and modify the clay properties in earth material to propose an innovative strategy to develop a castable earth-based material. To do so, we focused on the modification of clay properties at fresh state with inorganic additives. As the rheological behaviour of clays is controlled by their surface charge, the addition of phosphate anion allows discussing deep the rheology of concentrated clay suspensions. We highlighted the thixotropic and shear thickening behaviour of a dispersed kaolinite clay suspensions. Indeed, by adding sodium hexametaphosphate the workability of clay paste increases and the behaviour is stable during time after a certain shear is applied. Moreover, we stress that the aging and the shift in critical strain in clay system are due to the re-arrangement of clay suspension and a decrease of deformation during time. The understanding of both effect: thixotropy and aging are crucial for better processing of clay-based material and for self-compacting clay concrete. Yet, studies need to pursue to better understand the mechanism.
Fracture in Kaolinite clay suspensions
NASA Astrophysics Data System (ADS)
Kosgodagan Acharige, Sebastien; Jerolmack, Douglas J.; Arratia, Paulo E.
2017-11-01
Clay minerals are involved in many natural (landslides, river channels) and industrial processes (ceramics, cosmetics, oil recovery). They are plate shaped charged colloids and exhibit different flow properties than simpler colloids when suspended in a liquid such as thixotropy and shear-banding. kaolinite platelets are non-swelling, meaning that the stacks formed by the platelets do not have water layers, and thus the suspension does not have a sol-gel transition. However, it has been shown that kaolinite suspensions possesses a non-zero yield stress even at low concentrations, indicating that the particles arrange themselves in a structure through attractive interactions. Here, we experimentally investigate the sedimentation of kaolinite suspensions in a Hele-Shaw cell. The sedimentation of these dilute suspensions can display solid behavior like fracture, revealed in cross-polarized light, which is linked to the failure of the weakly-bonded structure (typical yield stress 10-2 Pa). By changing the interaction potential of the particles (by sonication or introducing salts), we show through these sedimentation experiments, how the fracture pattern can be avoided. Research was sponsored by the Army Research Laboratory and was accomplished under Grant Number 569074.
1988-08-01
self-supporting films, and aqueous slurries. IR spectra were obtained for kaolinite and montmorillonite clays as well as for p-xylene adsorbed on...proportional to OC and Xs. They also reported that the sorption of chloroethanes on sand, montmorillonite , and kaolinite was too small (< 2 ng/g soil...Ca- montmorillonite and Ca-kaolin at fractional surface coverages of only 0.65 and 0.35, respectively. C values for their montmorillonite and kaolinite
Effect of clay type on the velocity and run-out distance of cohesive sediment gravity flows
NASA Astrophysics Data System (ADS)
Baker, Megan; Baas, Jaco H.; Malarkey, Jonathan; Kane, Ian
2016-04-01
Novel laboratory experiments in a lock-exchange flume filled with natural seawater revealed that sediment gravity flows (SGFs) laden with kaolinite clay (weakly cohesive), bentonite clay (strongly cohesive) and silica flour (non-cohesive) have strongly contrasting flow properties. Knowledge of cohesive clay-laden sediment gravity flows is limited, despite clay being one of the most abundant sediment types on earth and subaqueous SGFs transporting the greatest volumes of sediment on our planet. Cohesive SGFs are particularly complex owing to the dynamic interplay between turbulent and cohesive forces. Cohesive forces allow the formation of clay flocs and gels, which increase the viscosity and shear strength of the flow, and attenuate shear-induced turbulence. The experimental SGFs ranged from dilute turbidity currents to dense debris flows. For each experiment, the run-out distance, head velocity and thickness distribution of the deposit were measured, and the flow properties were recorded using high-resolution video. Increasing the volume concentration of kaolinite and bentonite above 22% and 17%, respectively, reduced both the maximum head velocity and the run-out distances of the SGFs. We infer that increasing the concentration of clay particles enhances the opportunity for the particles to collide and flocculate, thus increasing the viscosity and shear strength of the flows at the expense of turbulence, and reducing their forward momentum. Increasing the volume concentration in the silica-flour laden flows from 1% to 46% increased the maximum head velocity, owing to the gradual increase in excess density. Thereafter, however, intergranular friction is inferred to have attenuated the turbulence, causing a rapid reduction in the maximum head velocity and run-out distance as suspended sediment concentration was increased. Moving from flows carrying bentonite via kaolinite to silica flour, a progressively larger volumetric suspended sediment concentration was needed to produce similar run-out distances and maximum head velocities. Strongly cohesive bentonite flows were able to create a stronger network of particle bonds than weakly cohesive kaolinite flows of a similar concentration, thus producing the lower maximum head velocities and run-out distances observed. The lack of cohesion in the silica-flour laden flows meant that extremely high suspended sediment concentrations, i.e. close to the cubic packing density, were required to produce a high enough frictional strength to reduce the forward momentum of these flows. These experimental results can be used to improve our understanding of the deposit geometry and run-out distance of fine-grained SGFs in the natural environment. We suggest that natural SGFs that carry weakly cohesive clays (e.g. kaolinite) reach a greater distance from their origin than flows that contain strongly cohesive clays (e.g. bentonite) at similar suspended sediment concentrations, whilst equivalent fine-grained, non-cohesive SGFs travel the furthest. In addition, weakly cohesive SGFs may cover a larger surface area and have thinner deposits, with important ramifications for the architecture of stacked event beds.
Otto, Caitlin C.; Kilbourne, Jacquelyn
2016-01-01
Discoveries associated with antibacterial activity of hydrated clays necessitate assessments of in vivo efficacy, practical use and safety. Surface properties of clays can lead to variations in the composition and abundance of bound compounds or ions, thus affecting antibacterial activity. Since exchangeable metal ions released from the clay surface are responsible for in vitro antibacterial activity, we evaluated the in vivo antibacterial efficacy of four natural clays (one illite clay, two montmorillonite clays and one kaolinite clay) and three ion-exchanged, antibacterial clays against superficial, cutaneous meticillin-resistant Staphylococcus aureus (MRSA) infections in mice. Superficial, cutaneous wounds on the back of SKH1-Elite mice were generated and subsequently infected with MRSA. Following twice daily applications of a hydrated clay poultice to infected wounds for 7 days, we observed significant differences in the in vivo antibacterial efficacy between different types of clays. The natural and ion-exchanged illite clays performed best, as measured by bacterial load, inflammatory response and gross wound morphology with significant decreases in bacterial viability and dermatitis. Topical application of kaolinite clay was the least effective, resulting in the lowest decrease in bacterial load and exhibiting severe dermatitis. These data suggest that specific types of clays may offer a complementary and integrative strategy for topically treating MRSA and other cutaneous infections. However, since natural clays exhibit in vitro antibacterial variability and vary vastly in surface chemistries, adsorptive/absorptive characteristics and structural composition, the properties and characteristics of illite clays could aid in the development of standardized and customized aluminosilicates for topical infections. PMID:26508716
Latest Paleocene lithologic and biotic events in neritic deposits of southwestern New Jersey
Gibson, Thomas G.; Bybell, Laurel M.; Owens, James P.
1993-01-01
In the southwestern New Jersey Coastal Plain, four drill holes contain continuous neritic sedimentation across the Paleocene/Eocene boundary (calcareous nannofossil Zone NP 9/NP 10 boundary). Significant lithologic and biotic changes occur in these strata near the top of the Paleocene. Global warming, increased precipitation, and other oceanographic and climatic events that have been recognized in high-latitude, deep-oceanic deposits of the latest Paleocene also influenced mid-latitude, shallow-marine, and terrestrial environments of the western North Atlantic. The diverse, well-preserved calcareous nannofossil flora that is present throughout the entire New Jersey boundary section accurately places these events within the uppermost part of the upper Paleocene Zone NP 9. Several rapid but gradational changes occur within a 1.1-m interval near the top of Zone NP 9. The changes include (1) a change in lithology from glauconitic quartz sand to clay, (2) a change in clay mineral suites from illite/smectite-dominated to kaolinite-dominated, (3) a change in benthic foraminiferal assemblages to a lower diversity fauna suggestive of low-oxygen environments, (4) a significant increase in planktonic foraminiferal abundance, and (5) an increased species turnover rate in marine calcareous nannofossils. Pollen was sparse in the New Jersey drill holes, but terrestrial sporomorph species in Virginia exhibit increased turnover rates at a correlative level. Foraminiferal assemblages and lithology indicate that relative sea level rose in New Jersey at the same time as these late Paleocene events occurred in late Biochron NP 9. The higher sea levels influenced sediment type and absolute abundance of planktonic foraminifers in the deposits. Above the initial increase of kaolinite in the upper part of Zone NP 9, the kaolinite percentage continues to increase, and the maximum kaolinite value occurs in the uppermost part of Zone NP 9. There are few changes in either the sediments or the biota precisely at the Zone NP 9/NP 10 boundary in New Jersey. The clay-rich deposits with a high kaolinite clay mineral suite, the lowered diversity benthic foraminiferal assemblages, the abundant planktonic foraminiferal specimens, and the calcareous nannofossil assemblages continued essentially unchanged into the earliest Eocene Zone NP 10. Within the lower part of Zone NP 10, the kaolinite percentage decreased to very low values.
NASA Technical Reports Server (NTRS)
Rudd, Lawrence; Merenyi, Erzsebet
2004-01-01
Worldwide debris flows destroy property and take human lives every year (Costa, 1984). As a result of extensive property damage and loss of life there is a pressing need to go beyond just describing the nature and extent of debris flows as they occur. Most of the research into debris-flow initiation has centered on rainfall, slope angle, and existing debris-flow deposits (Costa and Wieczorek, 1987). The factor of source lithology has been recently addressed by studies in the sedimentary terranes of Grand Canyon (Webb et al., 1996; Griffiths et al., 1996) and on the Colorado Plateau as a whole.3 On the Colorado Plateau shales dominated by kaolinite and illite clays are significantly more likely to be recent producers of debris-flows than are shales in which smectite clays dominate.3 Establishing the location of shales and colluvial deposits containing kaolinite and illite clays in sedimentary terranes on the Colorado Plateau is essential to predicting where debris flows are likely to occur. AVIRIS imagery can be used to distinguish between types of clay minerals (Chabrillat et al., 2001), providing the basis for surface-materials maps. The ultimate product of this study will be a model that can be used to estimate the debris-flow hazard in Cataract Canyon, Utah. This model will be based on GIS overlay analysis of debris-flow initiation factor maps, including surface-materials maps derived from AVIRIS data.
NASA Astrophysics Data System (ADS)
Fox, Aryeh; Packman, Aaron I.; Boano, Fulvio; Phillips, Colin B.; Arnon, Shai
2018-05-01
Fine particle deposition and streambed clogging affect many ecological and biogeochemical processes, but little is known about the effects of groundwater flow into and out of rivers on clogging. We evaluated the effects of losing and gaining flow on the deposition of suspended kaolinite clay particles in a sand streambed and the resulting changes in rates and patterns of hyporheic exchange flux (HEF). Observations of clay deposition from the water column, clay accumulation in the streambed sediments, and water exchange with the bed demonstrated that clay deposition in the bed substantially reduced both HEF and the size of the hyporheic zone. Clay deposition and HEF were strongly coupled, leading to rapid clogging in areas of water and clay influx into the bed. Local clogging diverted exchanged water laterally, producing clay deposit layers that reduced vertical hyporheic flow and favored horizontal flow. Under gaining conditions, HEF was spatially constrained by upwelling water, which focused clay deposition in a small region on the upstream side of each bed form. Because the area of inflow into the bed was smallest under gaining conditions, local clogging required less clay mass under gaining conditions than neutral or losing conditions. These results indicate that losing and gaining flow conditions need to be considered in assessments of hyporheic exchange, fine particle dynamics in streams, and streambed clogging and restoration.
Remobilization of toxic heavy metals adsorbed to bacterial wall-clay composites.
Flemming, C A; Ferris, F G; Beveridge, T J; Bailey, G W
1990-01-01
Significant quantities of Ag(I), Cu(II), and Cr(III) were bound to isolated Bacillus subtilis 168 walls, Escherichia coli K-12 envelopes, kaolinite and smectite clays, and the corresponding organic material-clay aggregates (1:1, wt/wt). These sorbed metals were leached with HNO3, Ca(NO3)2, EDTA, fulvic acid, and lysozyme at several concentrations over 48 h at room temperature. The remobilization of the sorbed metals depended on the physical properties of the organic and clay surfaces and on the character and concentration of the leaching agents. In general, the order of remobilization of metals was Cr much less than Ag less than Cu. Cr was very stable in the wall, clay, and composite systems; pH 3.0, 500 microM EDTA, 120-ppm [mg liter-1] fulvic acid, and 160-ppm Ca remobilized less than 32% (wt/wt) of sorbed Cr. Ag (45 to 87%) and Cu (up to 100%) were readily removed by these agents. Although each leaching agent was effective at mobilizing certain metals, elevated Ca or acidic pH produced the greatest overall mobility. The organic chelators were less effective. Lysozyme digestion of Bacillus walls remobilized Cu from walls and Cu-wall-kaolinite composites, but Ag, Cr, and smectite partially inhibited enzyme activity, and the metals remained insoluble. The extent of metal remobilization was not always dependent on increasing concentrations of leaching agents; for example, Ag mobility decreased with some clays and some composites treated with high fulvic acid, EDTA, and lysozyme concentrations. Sometimes the organic material-clay composites reacted in a manner distinctly different from that of their individual counterparts; e.g., 25% less Cu was remobilized from wall- and envelope-smectite composites than from walls, envelopes, or smectite individually in 500 microM EDTA. Alternatively, treatment with 160-ppm Ca removed 1.5 to 10 times more Ag from envelope-kaolinite composites than from the individual components. The particle size of the deposited metal may account for some of the stability changes; those metals that formed large, compact aggregates (Cr and Ag) as seen by transmission electron microscopy were less likely to be remobilized. In summary, it is apparent that remobilization of toxic heavy metals in sediments, soils, and the vadose zone is a complicated issue. Predictions based on single inorganic or organic component systems are too simplistic. Images PMID:2126702
Program and Abstracts for Clay Minerals Society 28th Annual Meeting
NASA Technical Reports Server (NTRS)
1991-01-01
This volume contains abstracts that were accepted for presentation at the annual meeting. Some of the main topics covered include: (1) fundamental properties of minerals and methods of mineral analysis; (2) surface chemistry; (3) extraterrestrial clay minerals; (4) geothermometers and geochronometers; (5) smectite, vermiculite, illite, and related reactions; (6) soils and clays in environmental research; (7) kaolinite, halloysite, iron oxides, and mineral transformations; and (8) clays in lakes, basins, and reservoirs.
Ice formation on kaolinite: Insights from molecular dynamics simulations
NASA Astrophysics Data System (ADS)
Sosso, Gabriele C.; Tribello, Gareth A.; Zen, Andrea; Pedevilla, Philipp; Michaelides, Angelos
2016-12-01
The formation of ice affects many aspects of our everyday life as well as important technologies such as cryotherapy and cryopreservation. Foreign substances almost always aid water freezing through heterogeneous ice nucleation, but the molecular details of this process remain largely unknown. In fact, insight into the microscopic mechanism of ice formation on different substrates is difficult to obtain even if state-of-the-art experimental techniques are used. At the same time, atomistic simulations of heterogeneous ice nucleation frequently face extraordinary challenges due to the complexity of the water-substrate interaction and the long time scales that characterize nucleation events. Here, we have investigated several aspects of molecular dynamics simulations of heterogeneous ice nucleation considering as a prototypical ice nucleating material the clay mineral kaolinite, which is of relevance in atmospheric science. We show via seeded molecular dynamics simulations that ice nucleation on the hydroxylated (001) face of kaolinite proceeds exclusively via the formation of the hexagonal ice polytype. The critical nucleus size is two times smaller than that obtained for homogeneous nucleation at the same supercooling. Previous findings suggested that the flexibility of the kaolinite surface can alter the time scale for ice nucleation within molecular dynamics simulations. However, we here demonstrate that equally flexible (or non flexible) kaolinite surfaces can lead to very different outcomes in terms of ice formation, according to whether or not the surface relaxation of the clay is taken into account. We show that very small structural changes upon relaxation dramatically alter the ability of kaolinite to provide a template for the formation of a hexagonal overlayer of water molecules at the water-kaolinite interface, and that this relaxation therefore determines the nucleation ability of this mineral.
NASA Astrophysics Data System (ADS)
Fernandez-Ugalde, O.; Barré, P.; Hubert, F.; Virto, I.; Chenu, C.; Ferrage, E.; Caner, L.
2012-12-01
Aggregation is a key process for soil functioning as it influences C storage, vulnerability to erosion and water holding capacity. While the influence of soil organic C on aggregation has been documented, much less is known about the role of soil mineralogy. Soils usually contain a mixture of clay minerals with contrasted surface properties, which should result on different abilities of clay minerals to aggregation. We took advantage of the intrinsic mineral heterogeneity of a temperate Luvisol to compare the role of clay minerals (illite, smectite, kaolinite, and mixed-layer illite-smectite) in aggregation. In a first step, grassland and tilled soil samples were fractionated in water in aggregate-size classes according to the hierarchical model of aggregation (Tisdall and Oades, 1982). Clay mineralogy and organic C in the aggregate-size classes were analyzed. The results showed that interstratified minerals containing swelling phases accumulated in aggregated fractions (>2 μm) compared to free clay fractions (<2 μm) in the two land-uses. The accumulation increased from large macro-aggregates (>500 μm) to micro-aggregates (50-250 μm). C concentration and C/N ratio followed the opposite trend. These results constitute a clay mineral-based evidence for the hierarchical model of aggregation, which postulates an increasing importance of the reactivity of clay minerals in the formation of micro-aggregates compared to larger aggregates. In the latter aggregates, formation relies on the physical enmeshment of particles by fungal hyphae, and root and microbial exudates. In a second step, micro-aggregates from the tilled soil samples were submitted to increasingly disaggregating treatments by sonication to evaluate the link between their water stability and clay mineralogy. Micro-aggregates with increasing stability showed an increase of interstratified minerals containing swelling phases and C concentration for low intensities of disaggregation (from 0 to 5 J mL-1). This suggests that swelling phases promote their stability. Swelling phases and organic C decreased for greater intensities of disaggregation. These results and the SEM images taken at different disaggregation intensities indicate that when increasing disaggregation intensity above 5 J mL-1, the recovered material consists on sand particles covered by physical coatings of illite and kaolinite. Our results show that different clay minerals have different contribution to soil aggregation. Swelling phases are especially important for water-stable aggregates formation, whereas illite and kaolinite can either contribute to aggregation or been coated to sand grains in "mineral aggregates", without porosity and organic C protection capability. In conclusion, soils with large proportion of swelling clay minerals have greater potential for carbon storage by occlusion in aggregates and greater resistance to erosion. Tisdall JM, Oades JM (1982) Organic matter and water-stable aggregates in soils. J Soil Sci 62: 141-163.
NASA Technical Reports Server (NTRS)
Coyne, L.; Mariner, R.; Rice, A.
1991-01-01
Air oxidation of hydrazine was studied by using a group of kaolinites, halloysites, and substituent oxides as models for the tetrahedral and octahedral sheets. The rate was found to be linear with oxygen. The stoichiometry showed that oxygen was the primary oxidant and that dinitrogen was the only important nitrogen-containing product. The rates on kaolinites were strongly inhibited by water. Those on three-dimensional silica and gibbsite appeared not to be. That on a supposedly layered silica formed from a natural kaolinite by acid leaching showed transitional behavior--slowed relative to that expected from a second-order reaction relative to that on the gibbsite and silica but faster than those on the kaolinites. The most striking result of the reaction was the marked increase in the rate of reaction of a constant amount of hydrazine as the amount of clay was increased. The increase was apparent (in spite of the water inhibition at high conversions) over a 2 order of magnitude variation of the clay weight. The weight dependence was taken to indicate that the role of the clay is very important, that the number of reactive centers is very small, or that they may be deactivated over the course of the reaction. In contrast to the strong dependence on overall amount of clay, the variation of amounts of putative oxidizing centers, such as structural Fe(III), admixed TiO2 or Fe2O3, or O- centers, did not result in alteration of the rate commensurate with the degree of variation of the entity in question. Surface iron does play some role, however, as samples that were pretreated with a reducing agent were less active as catalysts than the parent material. These results were taken to indicate either that the various centers interact to such a degree that they cannot be considered independently or that the reaction might proceed by way of surface complexation, rather than single electron transfers.
NASA Technical Reports Server (NTRS)
Jackson, T. A.
1971-01-01
Experiments on the polymerization of the L- and D-optical isomers of aspartic acid and serine using kaolinite as a catalyst showed that the L-optical isomers were polymerized at a much higher rate than the D-optical isomers; racemic (DL-) mixtures were polymerized at an intermediate rate. The peptides formed from the L-monomers were preferentially adsorbed by the clay. In the absence of kaolinite, no significant or consistent difference in the behavior of the L- and D-optical isomers was observed. In experiments on the adsorption of L- and D-phenylalanine by kaolinite, the L-optical isomer was preferentially adsorbed.
Presti, Davide; Pedone, Alfonso; Mancini, Giordano; Duce, Celia; Tiné, Maria Rosaria; Barone, Vincenzo
2016-01-21
Density functional theory calculations and classical molecular dynamics simulations have been used to investigate the structure and dynamics of water molecules on kaolinite surfaces and confined in the interlayer of a halloysite model of nanometric dimension. The first technique allowed us to accurately describe the structure of the tetrahedral-octahedral slab of kaolinite in vacuum and in interaction with water molecules and to assess the performance of two widely employed empirical force fields to model water/clay interfaces. Classical molecular dynamics simulations were used to study the hydrogen bond network structure and dynamics of water adsorbed on kaolinite surfaces and confined in the halloysite interlayer. The results are in nice agreement with the few experimental data available in the literature, showing a pronounced ordering and reduced mobility of water molecules at the hydrophilic octahedral surfaces of kaolinite and confined in the halloysite interlayer, with respect to water interacting with the hydrophobic tetrahedral surfaces and in the bulk. Finally, this investigation provides new atomistic insights into the structural and dynamical properties of water-clay interfaces, which are of fundamental importance for both natural processes and industrial applications.
A Scale Model of Cation Exchange for Classroom Demonstration.
ERIC Educational Resources Information Center
Guertal, E. A.; Hattey, J. A.
1996-01-01
Describes a project that developed a scale model of cation exchange that can be used for a classroom demonstration. The model uses kaolinite clay, nails, plywood, and foam balls to enable students to gain a better understanding of the exchange complex of soil clays. (DDR)
NASA Astrophysics Data System (ADS)
Ahmad, A.; Lopulisa, C.; Imran, A. M.; Baja, S.
2018-05-01
Intensive cropping in the tropical region always becomes one of important driving forces of soil degradation. The primary aim of this study is to analyze the states and the dynamics of soil physicochemical properties to evaluate soil degradation in the tropical region a high rainfall on agricultural areas in South Sulawesi. A number of soil characteristics were analyzed for physical and chemical properties, and clay minerals with X-ray diffractometer. The degree of soil degradation is determined using Wischmeier and Smith equation. This study reveals that mean annual precipitation in 1979-2016 ranged from 1853.15 to 2981.30 mm/year. For land used for paddy field, palm oil, cacao and coffee plantation, the texture dominated with silt loam-clay loam, cation exchange capacity was 18.63-26.32 cmol+ kg-1, 0.98-2.91% of C-organic, 32-55% of base saturation, 0.1-3.5 cm h-1 of permeability, soil clay minerals were montmorillonite-kaolinite-halloysite, and the index erodibility was 0.3-0.5. Land used for mixed plants and shrubs, the texture dominated with silt loam-sandy clay loam, cation exchange capacity was 18.63-27.12 cmol+ kg-1, 1.09-2.89% of C-organic, 32-55% of base saturation, 0.2-4.9 cm/h of permeability, soil clay minerals were kaolinite-halloysite, and index erodibility was 0.1-0.3. Land use for cultivated in the high intensity of rainfall has changed the physicochemical properties of soils, but cultivated in monoculture has at some degree increased soil erodibility.
NASA Astrophysics Data System (ADS)
Lutfalla, Suzanne; Barré, Pierre; Bernard, Sylvain; Le Guillou, Corentin; Alléon, Julien; Chenu, Claire
2016-04-01
Better understanding the mechanisms responsible for the pluri-decadal persistence of carbon in soils requires well constraining the dynamics, the distribution and the chemical nature of both the soil organic carbon (SOC) and the associated mineral phases. The question we address in this work is whether different mineral species lead to different organo-mineral interactions and stabilize different quantities of SOM and different types of SOC. Here, benefiting from the unique opportunity offered by an INRA long term bare fallow (LTBF) experiment having started in 1928 in Versailles (France), we report the in-situ characterization of SOC dynamics in four clay fractions of this silty loam soil (total clays [TC, <2μm], coarse clays [CC, 0.2-2μm], intermediate clays [IC, 0.05-0.2μm] and fine clays [FC, 0-0.05μm]). The IC and FC fractions only contain smectite and illite/smectite mixed-layered clay minerals while the CC fraction also contains illite and kaolinite. In the absence of any carbon input, the plant-free LTBF clay fractions from Versailles progressively lost SOC during the first 50 years of the experiment, until they reached a seemingly stable concentration. Of note, the investigated clay fractions did not lose the same amount of SOC and do not exhibit the same final carbon concentrations. The decrease of the organic C:N ratios with LTBF duration corresponds to a progressive enrichment in N-rich SOC for all fractions which can be attributed to microbial material. Even though the speciation of SOC appears to only slightly evolve with LTBF duration, an enrichment in carboxyl and carbonyl groups is revealed by bulk-scale C-NEXAFS data for SOC from all clay fractions. In addition, STXM-based NEXAFS investigations at the submicrometer scale reveal three types of SOC-clay assemblages in addition to clay-free SOC and organic-free clays. While SOC appears mostly adsorbed onto clay surfaces within the IC and FC fractions, other protection mechanisms occur within the CC fraction. Altogether, the present study suggests that smectite have more efficient protection capabilities than those of illite and kaolinite.
NASA Astrophysics Data System (ADS)
Christofoletti, Sergio Ricardo; Torres Moreno, Maria Margarita; Batezelli, Alessandro; Zanardo, Antenor
2014-05-01
The Corumbataí Formation is a geological unit of the Paraná Basin comprises a range of predominantly argillaceous facies. These clays are important from an economic point of view, because they represent important mineral deposits suppliers of raw materials for the ceramic industry in the production of ceramic tiles.The study presents preliminary results of a research that aims to study the clays municipalities Tambaú, Ferreira and Santa Rosa of Viterbo in the State of São Paulo for their application and diversification of ceramic products. The methodology used was based on a detailed description of facies using the methodology in principles of analysis of Basin Miall (1984), followed by mineralogical identification by X-ray Diffraction, chemical analysis of major elements by X-ray Fluorescence and technological tests ceramic. According to the geological surveys of mines studied through columnar sections were identified the following lithofacies from base to top: Massive, Laminated, Intercalated and Altered. The mineralogy present on these lithofacies is composed by minerals: quartz, microclineo, albite, calcite, dolomite and hematite and by clay minerals illite, kaolinite and montmorillonite. The quartz represents the mineral more present in diffraction and occurs with d001 of 3.33Å in all lithofacies studied. The illite clay mineral represents the most frequent in studied samples presenting d 001 10Å in three conditions (natural, heated and treated with ethylene glycol) in which the blade was subjected to the analysis of X-ray diffraction, the presence of kaolinite or montmorillonite occurs or not in samples. It was observed a increased frequency of some minerals in the lithofacies studied, carbonates (calcite and dolomite), hematite and feldspar occurring in the intermediate portions of the profile with a predominance in lithofacies Intercalated. The illita clay mineral occurs throughout the profile, but with greater frequency in the lithofacies Massive and Laminated. The clay minerals kaolinite and montmorillonite occur in portions intermediate and top of the profiles studied in the intercalated and altered lithofacies. The chemical results of major elements by X-ray fluorescence confirmed the mineralogical results, with average values of 63.74 % of SiO2, 12.50 of Al2O3, 4.35% of of K2O, 0.45% of Na2O, 2,72% of CaO and 1,87 of MgO. The results chemical and mineralogical subsidized testing and ceramic formulations due to be executed later so defining the main applications of these clays in the production of ceramic products. The authors acknowledge the finantial support of Fundação de Amparo à Pesquisa do Estado de São Paulo-FAPESP, (Process, number 2012/24219-9).
Experimental Evaluation of pH and Temperature Effects on the Adsorption of Boron onto Clay Minerals
NASA Astrophysics Data System (ADS)
Hoenisch, B.; Marone, D.; Ruprecht, J.
2017-12-01
Modeling the secular evolution of the concentration [B] and isotopic composition (δ11B) of boron in seawater is hampered by limited constraints on the relative sources (i.e. riverine input of weathering products, hydrothermal convection at mid-ocean ridges and fluids expelled from accretionary prisms) and sinks (i.e. alteration of the oceanic crust, adsorption onto clays, and co-precipitation in carbonates) of boron to and from the ocean. Clays remove approximately 28% of total boron from the ocean and quantification of this sink thus represents a major factor for reconstructing the secular evolution of seawater [B] and δ11B over the Cenozoic. However, the relative strength of the clay sink could have been much smaller in the early Cenozoic compared to today, because borate ion as the charged species is preferentially adsorbed onto detrital clays over boric acid, and because the relative abundance of borate in seawater should have been lower under the more acidic conditions of the early Cenozoic. In addition, different clay minerals tend to fractionate boron isotopes differentially, and the relative composition of clay minerals has varied in the past with the dominant climate and weathering patterns on the continents. We have conducted a range of pH (7.5-8.4) and temperature (3-32°C) experiments with four clay minerals (Kaolinite, Illite, Montmorillonite and Chlorite), to build on previously published but limited experimental data. Similar to a previous study and as expected based on the relative abundance of borate ion in seawater, boron adsorption onto these clays increases at higher pH and lower temperatures, but whereas Montmorillonite and Illite absorb similar quantities of boron, Kaolinite is most and Chlorite least efficient in this process. We are now in the process of characterizing the boron isotope fractionation associated with these adsorption experiments.
Acidity of edge surface sites of montmorillonite and kaolinite
NASA Astrophysics Data System (ADS)
Liu, Xiandong; Lu, Xiancai; Sprik, Michiel; Cheng, Jun; Meijer, Evert Jan; Wang, Rucheng
2013-09-01
Acid-base chemistry of clay minerals is central to their interfacial properties, but up to now a quantitative understanding on the surface acidity is still lacking. In this study, with first principles molecular dynamics (FPMD) based vertical energy gap technique, we calculate the acidity constants of surface groups on (0 1 0)-type edges of montmorillonite and kaolinite, which are representatives of 2:1 and 1:1-type clay minerals, respectively. It shows that tbnd Si-OH and tbnd Al-OH2OH groups of kaolinite have pKas of 6.9 and 5.7 and those of montmorillonite have pKas of 7.0 and 8.3, respectively. For each mineral, the calculated pKas are consistent with the experimental ranges derived from fittings of titration curves, indicating that tbnd Si-OH and tbnd Al-OH2OH groups are the major acidic sites responsible to pH-dependent experimental observations. The effect of Mg substitution in montmorillonite is investigated and it is found that Mg substitution increases the pKas of the neighboring tbnd Si-OH and tbnd Si-OH2 groups by 2-3 pKa units. Furthermore, our calculation shows that the pKa of edge tbnd Mg-(OH2)2 is as high as 13.2, indicating the protonated state dominates under common pH. Together with previous adsorption experiments, our derived acidity constants suggest that tbnd Si-O- and tbnd Al-(OH)2 groups are the most probable edge sites for complexing heavy metal cations.
USDA-ARS?s Scientific Manuscript database
Selenate adsorption behavior was investigated on amorphous aluminum oxide, amorphous iron oxide, goethite, clay minerals: kaolinites, montmorillonites, illite, and 18 soil samples from Hawaii, and the Southwestern and the Midwestern regions of the US as a function of solution pH. Selenate adsorpti...
USDA-ARS?s Scientific Manuscript database
Selenite adsorption behavior was investigated on amorphous aluminum and iron oxides, clay minerals: kaolinite, montmorillonite, and illite, and 45 surface and subsurface soil samples from the Southwestern and Midwestern regions of the USA as a function of solution pH. Selenite adsorption decreased ...
NASA Astrophysics Data System (ADS)
Jeong, G. C.; Kim, M. G.; Choi, J. J.; Ryu, J. O.; Nho, J. G.; Choo, C. O.
2016-12-01
This study aims at estimating landslide-inducing factors such as extreme rainfall, slope, and geological factors in Busan city, southeastern Korea, using clay mineralogy, DM analysis and DB construction in order to develop the landslide evaluation standards suitable for the country. GIS-based data collected from the study area include geological maps, topological maps, soil maps, forest maps and others in the DB construction. Data extraction and processing for landslide-induced factors consist of expandable clay minerals identified using XRD, along with XRF and weathering sensitivity analysis and fundamental soil analysis on 38 bulk samples composed of weathered rocks and soils. Finally landslide sensibility maps were constructed using ArcGIS, together with ASTER satellite images for identifying clay minerals on regional areas helpful for saving time and money. In Mt. Cheonma, 16 samples are composed of quartz, albite, illite, vermiculite, and kaolinite, with little difference in mineralogy. In Mt. Hwangryeong and Mt. Geumryeun, 12 samples consist of quartz, albite, illite, vermiculite, kaolinite and hornblende, with little difference in mineralogy. In Mt. Songhak, 10 samples are composed of quartz, illite, vermiculite, and kaolinite. Quartz, albite and illite are abundant in most samples, regardless of sites studied. IDW interpolation method was applied to the Busan area. The resolution of space grids consists of 5 m x 5 m. Especially, illite was used as the most effective factor that induces landslide using IDW interpolation and ASTER satellite images. In conclusion, sensibility maps constructed using 16 layers including illite content, weathered sensibility are well in accordance with the real sites where landslides took place, showing that areas with high sensibility are closely related to the high frequencies of landslide. This research was supported by the Public Welfare & Safety Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (grant number 2012M3A2A1050976)
Microscopic Mechanism and Kinetics of Ice Formation at Complex Interfaces: Zooming in on Kaolinite
2016-01-01
Most ice in nature forms because of impurities which boost the exceedingly low nucleation rate of pure supercooled water. However, the microscopic details of ice nucleation on these substances remain largely unknown. Here, we have unraveled the molecular mechanism and the kinetics of ice formation on kaolinite, a clay mineral playing a key role in climate science. We find that the formation of ice at strong supercooling in the presence of this clay is about 20 orders of magnitude faster than homogeneous freezing. The critical nucleus is substantially smaller than that found for homogeneous nucleation and, in contrast to the predictions of classical nucleation theory (CNT), it has a strong two-dimensional character. Nonetheless, we show that CNT describes correctly the formation of ice at this complex interface. Kaolinite also promotes the exclusive nucleation of hexagonal ice, as opposed to homogeneous freezing where a mixture of cubic and hexagonal polytypes is observed. PMID:27269363
Some engineering aspects of homoionized mixed clay minerals.
Oren, Ali Hakan; Kaya, Abidin
2003-05-01
Many studies have been conducted to investigate the physicochemical behavior of pure clay minerals and predict their engineering performance in the field. In this study, the physicochemical properties of an artificial mixture of different clay minerals namely, 40-50% montmorillonite, 20-30% illite and 10-15% kaolin were investigated. The mixture was homoionized with sodium, Na+; calcium, Ca2+; and aluminum, Al3+. The engineering properties studied were consistency limits, sediment volume, compressibility behavior, and hydraulic conductivity. The results revealed that the liquid, plastic and shrinkage limits of soil increased with increasing cation valence. The hydraulic conductivity of the soil also increased with an increase in the valence of the cation at any given void ratio. Aluminum and sodium treated clays had the highest and the lowest modified compression index values, respectively. Furthermore, trivalent cation saturated clayey soil consolidates three times faster than that of monovalent and two times faster than that of divalent. These properties of the soils determined were, in general, similar to those of kaolinite rather than those of montmorillonite. The comparison of the results obtained with the published data in the literature revealed that the physicochemical behavior of the tested clay soil was, in general, similar to that of kaolinite.
Fatoyinbo, Henry O; McDonnell, Martin C; Hughes, Michael P
2014-07-01
Detection of pathogens from environmental samples is often hampered by sensors interacting with environmental particles such as soot, pollen, or environmental dust such as soil or clay. These particles may be of similar size to the target bacterium, preventing removal by filtration, but may non-specifically bind to sensor surfaces, fouling them and causing artefactual results. In this paper, we report the selective manipulation of soil particles using an AC electrokinetic microfluidic system. Four heterogeneous soil samples (smectic clay, kaolinitic clay, peaty loam, and sandy loam) were characterised using dielectrophoresis to identify the electrical difference to a target organism. A flow-cell device was then constructed to evaluate dielectrophoretic separation of bacteria and clay in a continous flow through mode. The average separation efficiency of the system across all soil types was found to be 68.7% with a maximal separation efficiency for kaolinitic clay at 87.6%. This represents the first attempt to separate soil particles from bacteria using dielectrophoresis and indicate that the technique shows significant promise; with appropriate system optimisation, we believe that this preliminary study represents an opportunity to develop a simple yet highly effective sample processing system.
Yankson, Kweku K.; Steck, Todd R.
2009-01-01
We present a simple strategy for isolating and accurately enumerating target DNA from high-clay-content soils: desorption with buffers, an optional magnetic capture hybridization step, and quantitation via real-time PCR. With the developed technique, μg quantities of DNA were extracted from mg samples of pure kaolinite and a field clay soil. PMID:19633108
Inyang, Hilary I; Bae, Sunyoung
2005-01-01
Physico-chemical interactions among polymer molecules in aqueous solution and clay mineralogical/textural characteristics influence the sorption of polymer molecules on clay barrier minerals. Amendment of potentially unstable barrier clays with aqueous polymers can improve barrier material resistance to environmental stresses during service. In this research, the ability of molecular coils of polyacrylamide (PAM) to overlap in solution and to enter interlayer space in Na-montmorillonite (specific surface=31.82+/-0.22 m2 g(-1)) and kaolinite (specific surface=18+/-2 m2 g(-1)) were analyzed theoretically and experimentally, using solution viscosity measurements, and X-ray diffractometry. Experimental data on two theoretical indices: relative size ratio (RSR); and molecular availability (Ma) that are formulated to scale polymer molecular sorption on clay interlayer, indicate that the sorption of PAM A (Mw=4000000) and PAM B (Mw=7000000) does not produce any significant change in the d-spacing of both clay minerals. Although the negative Ma values of -3.51 g l(-1) for PAM A and -3.88 g l(-1) for PAM B indicate high levels of entanglement of polymer molecular coils in solution, sorption data confirm that the entangled coils are still able to sorb onto Na-montmorillonite highly and kaolinite to a lesser extent.
Thermo Gravimetric and Differential Thermal Analysis of Clay of Western Rajasthan (india)
NASA Astrophysics Data System (ADS)
Shekhawat, M. S.
The paper presents the study of thermo gravimetric and differential thermal analysis of blended clay. Western part of Rajasthan (India) is rich resource of Ball clays and it is mainly used by porcelain, sanitary ware, and tile industry. The quality and grade of clay available in the region vary from one deposit to other. To upgrade the fired colour and strength properties, different variety of clays may be blended together. The paper compares the results of thermal analysis one of blended clay B2 with reference clay of Ukraine which is imported by industries owners. The result revealed that the blended clay is having mineral kaolinite while the Ukrainian clay is Halloysite.
Hosterman, John W.
1984-01-01
The Gulf of Mexico Coastal Plain produces approximately 85 percent of the ball clay used in the United States. The best commercial-grade clay deposits are composed of poorly crystalline kaolinite and small amounts of Md illite and (or) smectite. Sand and silt and iron oxide minerals are virtually absent, but quartz is present in the clay-size fraction. The best grade ball clays are found as lenses limited to the Wilcox Group (Paleocene and lower Eocene) and Claiborne Group (middle Eocene). Reserves of ball clay are sufficient for the present, but because of the lenticular nature of the clay bodies, close-spaced drilling, detailed sampling, mineralogic analyses, and ceramic testing are needed to prove future reserves.Approximately 11 percent of the total bentonite produced in the United States comes from the Gulf Coast region. The commercial-grade bentonites are composed primarily of smectite with little or no Md illite and kaolinite. The nonclay impurities are quartz, feldspar, muscovite, biotite, calcite, dolomite, gypsum, and heulandite. Commercial bentonites occur in the Upper Cretaceous formations in Alabama and Mississippi, in Paleocene formations in Mississippi and Tennessee, and in Eocene and Miocene formations in Texas. The demand for low-swelling bentonite of the Gulf Coastal Plain has not increased along with the demand for swelling bentonite; therefore the reserves are adequate.
Role of DDL processes during electrolytic reduction of Cu(II) in a low oxygen environment.
Brosky, Rebekah T; Pamukcu, Sibel
2013-11-15
Heavy metals typically accumulate in reduced bottom sediments after being discharged into waterways by industrial and municipal processes. A laboratory experiment was conducted in order to determine if abundance of clay in the bottom sediments of a Cu-contaminated aqueous ecosystem could enhance electrolytic reduction of the heavy metal. Cu(NO3)2 · 2.5H2O was added to simulate a moderately contaminated system with 650 μg Cu/ml kaolinite clay-water slurry. A constant electrical potential of 1.0 V/cm was applied across platinum wire electrodes inserted into the continuously stirred system for four days while the system ORP(2) was monitored and periodic sub-samples were taken for analysis. The electrical as well as the chemical results indicate that the quantity of Cu(II) being reduced to Cu(I), especially within the aqueous phase, is increased within the first 48 h of experimentation by the presence of kaolinite clay up to 0.05 mg clay/l slurry. Copyright © 2013 Elsevier B.V. All rights reserved.
Antimony(V) Adsorption by Variable-Charge Minerals
2013-10-01
6‒] and inner-sphere [≡SOSb(OH)5‒] adsorption mechanisms. In general, however, the models generated for single ligand systems required reoptimization...HCO3 and CO3 ) effectively desorbed Sb(V) from hydrous metal (Al and Fe) oxides, clay minerals, and Sb(V)-contaminated sediments, relative to the...temperatures (20- 22°C). 7 A well- crystallized Georgia kaolinite (KGa-1b) from the Source Clays Repository of The Clay Minerals Society (West Lafayette
Selenium isotope fractionation during adsorption onto the modified clay minerals
NASA Astrophysics Data System (ADS)
Xu, W.; Jianming, Z.; Tan, D.; Qin, H.
2016-12-01
Currently, Selenium (Se) isotopes have been used as a paleoenvironmental proxy to trace Se evolution in Ancient Ocean. And many researchers considered the variation of Se isotopes in nature mainly result from the reduction of Se oxyanion, while Se isotope fractionation during adsorption onto minerals was rarely reported. Therefore, based on the previous studies [1, 2], we used three common clay minerals in supergene environment: montmorillonite, illite and kaolinite as an adsorbent to study Se isotope fractionation during adsorption. Before doing adsorption experiments, the adsorbent were modified as Na-clay minerals to remove the possibility of interference of Ca2+, Fe3+, Fe2+ as well as organic matters. A batch adsorption experiments were carried out at room temperature (23 ±2 °) under N2 atmosphere, initial Se concentration (SeO32-/ SeO42-) was respectively 200ng and 100ng, the solution ionic strength was 0.1mol/L NaCl; the ratio of liquid to solid is 2g / L, and pH = 5. Experimental results showed that adsorption reached a steady state during 48h, and the maximum adsorption for SeO32- was larger than SeO42-. The isotope data showed that SeO42- adsorbed onto three clay minerals didn't present obvious Se isotope fractionation, generally δ82/78Se is less than 0.1 ‰. Meanwhile, SeO32- during adsorption process also didn't show the significant fractionation, less than 0.3 ‰. However, interestingly, for SeO32- the δ82/78Se values of solution during adsorption onto kaolinite underwent a process of increasing by 0.5‰ compared to the initial solution and then decreasing to 0.3‰. We speculated the reason may not be related to the surface charge of the clay minerals, but mostly with the layered structure of clay minerals. Montmorillonite and illite are 2: 1; kaolinite is 1: 1 layered structure. The different layered structure may influence the isotope fraction between Se oxyanions and clay minerals. These still needs further and more experiments to definitely explain this phenomenon. This work was financially supported by National Key Basic Research Program of China (2014CB238903) and Natural Science Foundation of China (41473028, 41273029). [1] D. Peak et al. Soil Science Society of America Journal. 2006, 192-203. [2] T. Missana et al. Journal of Colloid and Interface Science. 2009, 334, 132-138.
Phosphoric acid purification through different raw and activated clay materials (Southern Tunisia)
NASA Astrophysics Data System (ADS)
Trabelsi, Wafa; Tlili, Ali
2017-05-01
This study concerns the purification of Tunisian phosphoric acid produced by the Tunisian Chemical Group (TCG), using raw and activated clays materials from Southern Tunisia. The Gafsa basin clays samples (Jebel Hamadi (JHM); Jebel Stah (JS) and the El Hamma sample (Jebel Aïdoudi (JAD)) were activated with 3 M, HCl solution. Phosphoric acid purification was performed on raw and activated clays. Mineralogical characterisation was carried out using the X-ray powder diffraction method and infrared absorption spectroscopy. Textural changes between raw and activated clays were identified using SEM observations and specific surface analysis. Jebel Hamadi clays were almost dominated by smectite associated with kaolinite and illite traces, while Jebel Stah and Jebel Aïdoudi clays were composed of the association of smectite, illite and kaolinite. It is worth noting that the position of the smectite (001) reflection increased after the acidic activation in all studied samples, indicating the relaxation of the smectite structure along the c-axis. This was corroborated by the increasing specific surface area of the clay particles with the activation process. The specific surface area was close to 50 m2/g and 200 m2/g, for raw and activated materials, respectively. The maximum phosphoric acid purification was obtained by using activated clays with 3 N HCl for 4 h. This performance correlated with the maximum of the external specific surface area which generated strong acid sites. Furthermore, the best results of phosphoric acids purification from TCG were obtained at a specific consumption equivalent to 30 Kg of clay/ton of P2O5. These results showed that the best phosphoric acid purification was yielded by Jebel Aïdoudi clay. In all cases, the highest organic carbon reduction rates in the phosphoric acid after filtration were obtained at 90°C.
Švarcová, Silvie; Bezdička, Petr; Hradil, David; Hradilová, Janka; Žižak, Ivo
2011-01-01
Application of X-ray diffraction (XRD)-based techniques in the analysis of painted artworks is not only beneficial for indisputable identification of crystal constituents in colour layers, but it can also bring insight in material crystal structure, which can be affected by their geological formation, manufacturing procedure or secondary changes. This knowledge might be helpful for art historic evaluation of an artwork as well as for its conservation. By way of example of kaolinite, we show that classification of its crystal structure order based on XRD data is useful for estimation of its provenance. We found kaolinite in the preparation layer of a Gothic wall painting in a Czech church situated near Karlovy Vary, where there are important kaolin deposits. Comparing reference kaolin materials from eight various Czech deposits, we found that these can be differentiated just according to the kaolinite crystallinity. Within this study, we compared laboratory powder X-ray micro-diffraction (micro-XRD) with synchrotron radiation X-ray diffraction analysing the same real sample. We found that both techniques led to the same results.
The influence of aqueous phase properties (pH, ionic strength and divalent metal ion concentration) on clay particle zeta potential and packed-bed electro-osmotic permeability was quantified. Although pH strongly altered the zeta potential of a Georgia kaolinite, it did not signi...
Sorption of Cu and Pb to kaolinite-fulvic acid colloids: Assessment of sorbent interactions
NASA Astrophysics Data System (ADS)
Heidmann, Ilona; Christl, Iso; Kretzschmar, Ruben
2005-04-01
The sorption of Cu(II) and Pb(II) to kaolinite-fulvic acid colloids was investigated by potentiometric titrations. To assess the possible interactions between kaolinite and fulvic acid during metal sorption, experimental sorption isotherms were compared with predictions based on a linear additivity model (LAM). Suspensions of 5 g L -1 kaolinite and 0.03 g L -1 fulvic acid in 0.01 M NaNO 3 were titrated with Cu and Pb solutions, respectively. The suspension pH was kept constant at pH 4, 6, or 8. The free ion activities of Cu 2+ and Pb 2+ were monitored in the titration vessel using ion selective electrodes. Total dissolved concentrations of metals (by ICP-MS) and fulvic acid (by UV-absorption) were determined in samples taken after each titration step. The amounts of metals sorbed to the solid phase, comprised of kaolinite plus surface-bound fulvic acid, were calculated by difference. Compared to pure kaolinite, addition of fulvic acid to the clay strongly increased metal sorption to the solid phase. This effect was more pronounced at pH 4 and 6 than at pH 8, because more fulvic acid was sorbed to the kaolinite surface under acidic conditions. Addition of Pb enhanced the sorption of fulvic acid onto kaolinite at pH 6 and 8, but not at pH 4. Addition of Cu had no effect on the sorption of fulvic acid onto kaolinite. In the LAM, metal sorption to the kaolinite surface was predicted by a two-site, 1-pK basic Stern model and metal sorption to the fulvic acid was calculated with the NICA-Donnan model, respectively. The LAM provided good predictions of Cu sorption to the kaolinite-fulvic acid colloids over the entire range in pH and free Cu 2+ ion activity (10 -12 to 10 -5). The sorption of Pb was slightly underestimated by the LAM under most conditions. A fractionation of the fulvic acid during sorption to kaolinite was observed, but this could not explain the observed deviations of the LAM predictions from the experimental Pb sorption isotherms.
Bohor, B.F.
1990-01-01
The event terminating the Cretaceous period and the Mesozoic era caused massive extinctions of flora and fauna worldwide. Theories of the nature of this event can be classed as endogenic (volcanic, climatic, etc.) or exogenic (extraterrestrial causes). Mineralogical evidence from the boundary clays and claystones strongly favor the impact of an extraterrestrial body as the cause of this event. Nonmarine KT boundary claystones are comprised of two separate layers-an upper layer composed of high-angle ejecta material (shocked quartz, altered glass and spinel) and a basal kaolinitic layer containing spherules, clasts, and altered glass, together with some shocked grains. Recognition of this dual-layered nature of the boundary clay is important for the determination of the timing and processes involved in the impact event and in the assignment and interpretation of geochemical signatures. Multiple sets of shock-induced microdeformations (planar features) in quartz grains separated from KT boundary clays provide compelling evidence of an impact event. This mineralogical manifestation of shock metamorphism is associated worldwide with a large positive anomaly of iridium in these boundary clays, which has also been considered indicative of the impact of a large extraterrestrial body. Global distributions of maximum sizes of shocked quartz grains from the boundary clays and the mineralogy of the ejecta components favor an impact on or near the North American continent. Spinel crystals (magnesioferrite) occur in the boundary clays as micrometer-sized octahedra or skeletal forms. Their composition differs from that of spinels found in terrestrial oceanic basalts. Magnesioferrite crystals are restricted to the high-angle ejecta layer of the boundary clays and their small size and skeletal morphology suggest that they are condensation products of a vaporized bolide. Hollow spherules ranging up to 1 mm in size are ubiquitously associated with the boundary clays. In nonmarine sections, where a high-angle ejecta layer and an underlying kaolinitic layer can be distinguished, the spherules are found only in the kaolinitic layer. The morphologies and surface features of these spherules suggest that they are original forms, and not secondary growths or algal bodies. These impact spherules closely resemble microtektites in size and shape. All of these features of the boundary clay are uniquely associated with impact, and cannot have been formed by volcanic or other terrestrial processes. ?? 1990.
Rock Deformation at High Confining Pressure and Temperature.
debugged, delivered and installed to the contracting agency. Clay specimens of illite, kaolinite and montmorillonite were deformed in tri-axial compression...at 25 and 3000C at a constant confining pressure of 2 kb and a constant strain rate of .0001 sec. The illite and kaolinite are stronger under these...conditions than montmorillonite . Cores from dolomite single crystals were deformed at a confining pressure of 7 kb and temperatures of 300 and 500C
Influence of operational parameters on electro-Fenton degradation of organic pollutants from soil.
Rosales, E; Pazos, M; Longo, M A; Sanroman, M A
2009-09-01
The combination of the Fenton's reagent with electrochemistry (the electro-Fenton process) represents an efficient method for wastewater treatment. This study describes the use of this process to clean soil or clay contaminated by organic compounds. Model soil of kaolinite clay polluted with the dye Lissamine Green B (LGB) was used to evaluate the capability of the electro-Fenton process. The effects of operating parameters such as electrode material and dye concentration were investigated. Operating in an electrochemical cell under optimized conditions while using electrodes of graphite, a constant potential difference of 5 V, pH 3, 0.2 mM FeSO(4). 7H(2)O, and electrolyte 0.1 M Na(2)SO(4), around 80% of the LGB dye on kaolinite clay was decolorized after 3 hours with an electric power consumption around 0.15 W h g(-1). Furthermore, the efficiency of this process for the remediation of a real soil polluted with phenanthrene, a typical polycyclic aromatic hydrocarbon, has been demonstrated.
The Leaching of Aluminium In Spanish Clays, Coal Mining Wastes and Coal Fly Ashes by Sulphuric Acid.
NASA Astrophysics Data System (ADS)
Fernández, A. M.; Ibáñez, J. L.; Llavona, M. A.; Zapico, R.
The acid leaching of aluminium from several non traditional ores, bayerite, kaolinite, different clays, coal mining wastes and coal fly ashes, and the kinetic of their dissolution are described. The effects of time, temperature, acid concentration, sample calcination, particle size were examined. The leaching of aluminium is dependent on acid concentration and strongly on temperature. Generally, the time to reach a fixed percentage of dissolution decreases with increasing acid concentration in the range 6% to 40% acid by weight. On clays and coal mining wastes a good relation between Al removal and ratio kaolinite/illite was also observed at all temperatures and acid concentration tested. Coal fly ashes are particles that were heated at very high temperatures in the power station and Al compounds were transformed into mullite and so Al recovery was minor. Several rate equations describing the kinetics of the leach reaction were discussed and Kinetic parameters and activation energy values of samples are presented.
NASA Astrophysics Data System (ADS)
Do Campo, Margarita; Bauluz, Blanca; del Papa, Cecilia; White, Timothy; Yuste, Alfonso; Mayayo, Maria Jose
2018-06-01
The continental Paleocene-Eocene sequence investigated in this study belongs to the Salta Group, deposited in an intracontinental rift, the Salta Basin (NW Argentina), that evolved from the lower Cretaceous to the middle Paleogene, and is subdivided into the Pirgua, the Balbuena and the Santa Barbara Subgroups. The Maíz Gordo Formation (200 m thick) is the middle unit of the Santa Bárbara Subgroup, deposited during late post-rift sedimentation. We studied the mineralogy of fine-grained horizons of this formation by X-ray diffraction and Scanning Electron Microscopy (SEM) in order to examine the connection between vertical changes in clay mineralogy in alluvial sediments and paleosols, and global paleoclimatic changes registered during the Paleogene. Paleosols vary from calcic vertisols in the lowermost levels, to inseptisols and gleysols in intermediate positions, to gleyed oxisols in the upper section, indicating increased chemical weathering through time. Clay mineral relative abundances vary with a general increase in kaolinite content from bottom to top. However, at one site there are significant variations in kaolinite/muscovite (Kln/Ms) that define five cycles of kaolinite abundance and Kln/Ms. that indicate cyclic patterns of paleoprecipitation and paleotemperature. These are interpreted as several short-lived hyperthermals during the Paleocene-early Eocene in the Southern Hemisphere, which correlate with well-established episodes of warmth documented from the Northern Hemisphere.
Mineral Acquisition from Clay by Budongo Forest Chimpanzees.
Reynolds, Vernon; Lloyd, Andrew W; English, Christopher J; Lyons, Peter; Dodd, Howard; Hobaiter, Catherine; Newton-Fisher, Nicholas; Mullins, Caroline; Lamon, Noemie; Schel, Anne Marijke; Fallon, Brittany
2015-01-01
Chimpanzees of the Sonso community, Budongo Forest, Uganda were observed eating clay and drinking clay-water from waterholes. We show that clay, clay-rich water, and clay obtained with leaf sponges, provide a range of minerals in different concentrations. The presence of aluminium in the clay consumed indicates that it takes the form of kaolinite. We discuss the contribution of clay geophagy to the mineral intake of the Sonso chimpanzees and show that clay eaten using leaf sponges is particularly rich in minerals. We show that termite mound soil, also regularly consumed, is rich in minerals. We discuss the frequency of clay and termite soil geophagy in the context of the disappearance from Budongo Forest of a formerly rich source of minerals, the decaying pith of Raphia farinifera palms.
Mineral Acquisition from Clay by Budongo Forest Chimpanzees
Reynolds, Vernon; Lloyd, Andrew W.; English, Christopher J.; Lyons, Peter; Dodd, Howard; Hobaiter, Catherine; Newton-Fisher, Nicholas; Mullins, Caroline; Lamon, Noemie; Schel, Anne Marijke; Fallon, Brittany
2015-01-01
Chimpanzees of the Sonso community, Budongo Forest, Uganda were observed eating clay and drinking clay-water from waterholes. We show that clay, clay-rich water, and clay obtained with leaf sponges, provide a range of minerals in different concentrations. The presence of aluminium in the clay consumed indicates that it takes the form of kaolinite. We discuss the contribution of clay geophagy to the mineral intake of the Sonso chimpanzees and show that clay eaten using leaf sponges is particularly rich in minerals. We show that termite mound soil, also regularly consumed, is rich in minerals. We discuss the frequency of clay and termite soil geophagy in the context of the disappearance from Budongo Forest of a formerly rich source of minerals, the decaying pith of Raphia farinifera palms. PMID:26218593
NASA Astrophysics Data System (ADS)
Bout-Roumazeilles, V.; Riboulleau, A.; du Châtelet, E. Armynot; Lorenzoni, L.; Tribovillard, N.; Murray, R. W.; Müller-Karger, F.; Astor, Y. M.
2013-02-01
The mineralogical composition of 95 surface sediment samples from the Cariaco Basin continental shelf and Orinoco delta was investigated in order to constrain the clay-mineral main provenance and distribution within the Cariaco Basin. The spatial variability of the data set was studied using a geo-statistical approach that allows drawing representative clay-mineral distribution maps. These maps are used to identify present-day dominant sources for each clay-mineral species in agreement with the geological characteristics of the main river watersheds emptying into the basin. This approach allows (1) identifying the most distinctive clay-mineral species/ratios that determine particle provenance, (2) evaluating the respective contribution of local rivers, and (3) confirming the minimal present-day influence of the Orinoco plume on the Cariaco Basin sedimentation. The Tuy, Unare, and Neveri Rivers are the main sources of clay particles to the Cariaco Basin sedimentation. At present, the Tuy River is the main contributor of illite to the western part of the southern Cariaco Basin continental shelf. The Unare River plume, carrying smectite and kaolinite, has a wide westward propagation, whereas the Neveri River contribution is less extended, providing kaolinite and illite toward the eastern Cariaco Basin. The Manzanares, Araya, Tortuga, and Margarita areas are secondary sources of local influence. These insights shed light on the origin of present-day terrigenous sediments of the Cariaco Basin and help to propose alternative explanations for the temporal variability of clay mineralogy observed in previously published studies.
NASA Astrophysics Data System (ADS)
Sei, J.; Morato, F.; Kra, G.; Staunton, S.; Quiquampoix, H.; Jumas, J. C.; Olivier-Fourcade, J.
2006-10-01
Thirteen clay samples from four deposits in the Ivory Coast (West Africa) were studied using X-ray diffraction, thermogravimetric analysis and chemical analysis. Mineralogical, crystallographic and morphological characteristics of these samples are given. Kaolinite is the principal mineral but other minerals are present in small quantities: illite, quartz, anatase and iron oxides (oxides and oxyhydroxides). The crystallographic, morphological and surface characteristics are influenced by the presence of these impurities. In particular, the presence of iron oxides was associated with reduced structural ordering and thermal stability of kaolinite and increased specific surface area. These clays could be used in the ceramics industry to make tiles and bricks, and also in agronomy as supports for chemical fertilizers or for environmental protection by immobilising potentially toxic waste products.
Leach test of cladding removal waste grout using Hanford groundwater
DOE Office of Scientific and Technical Information (OSTI.GOV)
Serne, R.J.; Martin, W.J.; Legore, V.L.
1995-09-01
This report describes laboratory experiments performed during 1986-1990 designed to produce empirical leach rate data for cladding removal waste (CRW) grout. At the completion of the laboratory work, funding was not available for report completion, and only now during final grout closeout activities is the report published. The leach rates serve as inputs to computer codes used in assessing the potential risk from the migration of waste species from disposed grout. This report discusses chemical analyses conducted on samples of CRW grout, and the results of geochemical computer code calculations that help identify mechanisms involved in the leaching process. Themore » semi-infinite solid diffusion model was selected as the most representative model for describing leaching of grouts. The use of this model with empirically derived leach constants yields conservative predictions of waste release rates, provided no significant changes occur in the grout leach processes over long time periods. The test methods included three types of leach tests--the American Nuclear Society (ANS) 16.1 intermittent solution exchange test, a static leach test, and a once-through flow column test. The synthetic CRW used in the tests was prepared in five batches using simulated liquid waste spiked with several radionuclides: iodine ({sup 125}I), carbon ({sup 14}C), technetium ({sup 99}Tc), cesium ({sup 137}Cs), strontium ({sup 85}Sr), americium ({sup 241}Am), and plutonium ({sup 238}Pu). The grout was formed by mixing the simulated liquid waste with dry blend containing Type I and Type II Portland cement, class F fly ash, Indian Red Pottery clay, and calcium hydroxide. The mixture was allowed to set and cure at room temperature in closed containers for at least 46 days before it was tested.« less
NASA Astrophysics Data System (ADS)
Watson, E.; Werts, S. P.; Gelabert, M.
2016-12-01
Fires in the natural environment affect the physical, chemical, and biological properties of soils. However, fires may also alter the mineralogy of the geologic material in which it comes in contact. Previous experiments on high temperature alteration of clays indicate that dehydration, oxidation, and hydroxylation in clay minerals can occur progressively in that order at increasing temperatures up to 500°C. It is also well known that wildfire events can heat soils to these temperature ranges several centimeters deep. In this experiment, alterations in clay chemistry were used as a tool to investigate fire intensity along with the changing morphology of clay minerals. For data collection, small camp fires were set in York County, SC and temperatures were recorded using a datalogger system to 5 cm deep during the fire event. Control samples were taken adjacent to the fires to compare the changing morphology of the minerals when heated. Powder x-ray diffraction and scanning electron microscopy were used to identify the clay mineralogy. The clay from soil samples was identified as hydrous kaolinite, anhydrous kaolinite, and varying types of goethite. To observe the dehydration, oxidation, and hydroxylation of clay minerals, scanning electron microscopy with emission dispersive spectroscopy was used to identify the O/cation ratios present, which would indicate changes in the oxidation state of the clay minerals. By mapping the changes in O/cation ratios with temperature in silicates, we are able to trace the temperature of the sediments during fire events. This research suggests it may be possible to utilize these geochemical trends to aid in soil and sediment temperature investigations in both archeological and modern soil and surface process investigations.
Chemical Mechanisms of Toxic Solute Interactions with Soil Constituents
1993-04-01
been widely reported (References 125-127). However, in days such as montmorillonite and kaolinite , whose cations have been (partially) exchanged with...matrix-isolation methods were used to characterize the sorption of water and fuel compounds on a model soil consisting of montmorillonite clay. The...only under very dry conditions. 14. SUBJECT TERMS Montmorillonite clay, fuels, infrared 15 NUMBER Of PAGES spectroscopy, ultraviolet-visible
Particle size and X-ray analysis of Feldspar, Calvert, Ball, and Jordan soils
NASA Technical Reports Server (NTRS)
Chapman, R. S.
1977-01-01
Pipette analysis and X-ray diffraction techniques were employed to characterize the particle size distribution and clay mineral content of the feldspar, calvert, ball, and jordan soils. In general, the ball, calvert, and jordan soils were primarily clay size particles composed of kaolinite and illite whereas the feldspar soil was primarily silt-size particles composed of quartz and feldspar minerals.
NASA Astrophysics Data System (ADS)
Wolela, A.
2014-11-01
Diagenetic studied in hydrocarbon-prospective Mesozoic rift basins were carried out in the Blue Nile Basin (Ethiopia), Ulster Basin (United Kingdom) and Hartford Basin (United States of America). Alluvial fan, single and amalgamated multistorey meandering and braided river, deep and shallow perennial lake, shallow ephemeral lake, aeolian and playa mud-flat are the prominent depositional environments. The studied sandstones exhibit red bed diagenesis. Source area geology, depositional environments, pore-water chemistry and circulation, tectonic setting and burial history controlled the diagenetic evolution. The diagenetic minerals include: facies-related minerals (calcrete and dolocrete), grain-coating clay minerals and/or hematite, quartz and feldspar overgrowths, carbonate cements, hematite, kaolinite, illite-smectite, smectite, illite, chlorite, actinolite, laumontite, pyrite and apatite. Diversity of diagenetic minerals and sequence of diagenetic alteration can be directly related to depositional environment and burial history of the basins. Variation in infiltrated clays, carbonate cements and clay minerals observed in the studied sandstones. The alluvial fan and fluviatile sandstones are dominated by kaolinite, illite calcite and ferroan calcite, whereas the playa and lacustrine sandstones are dominated by illite-smectite, smectite-chlorite, smectite, chlorite, dolomite ferroan dolomite and ankerite. Albite, pyrite and apatite are predominantly precipitated in lacustrine sandstones. Basaltic eruption in the basins modified mechanically infiltrated clays to authigenic clays. In all the studied sandstones, secondary porosity predominates over primary porosity. The oil emplacement inhabited clay authigenesis and generation of secondary porosity, whereas authigenesis of quartz, pyrite and apatite continued after oil emplacement.
Molecular Treatment of Nano-Kaolinite Generations.
Táborosi, Attila; Szilagyi, Robert K; Zsirka, Balázs; Fónagy, Orsolya; Horváth, Erzsébet; Kristóf, János
2018-06-18
A procedure is developed for defining a compositionally and structurally realistic, atomic-scale description of exfoliated clay nanoparticles from the kaolinite family of phylloaluminosilicates. By use of coordination chemical principles, chemical environments within a nanoparticle can be separated into inner, outer, and peripheral spheres. The edges of the molecular models of nanoparticles were protonated in a validated manner to achieve charge neutrality. Structural optimizations using semiempirical methods (NDDO Hamiltonians and DFTB formalism) and ab initio density functionals with a saturated basis set revealed previously overlooked molecular origins of morphological changes as a result of exfoliation. While the use of semiempirical methods is desirable for the treatment of nanoparticles composed of tens of thousands of atoms, the structural accuracy is rather modest in comparison to DFT methods. We report a comparative survey of our infrared data for untreated crystalline and various exfoliated states of kaolinite and halloysite. Given the limited availability of experimental techniques for providing direct structural information about nano-kaolinite, the vibrational spectra can be considered as an essential tool for validating structural models. The comparison of experimental and calculated stretching and bending frequencies further justified the use of the preferred level of theory. Overall, an optimal molecular model of the defect-free, ideal nano-kaolinite can be composed with respect to stationary structure and curvature of the potential energy surface using the PW91/SVP level of theory with empirical dispersion correction (PW91+D) and polarizable continuum solvation model (PCM) without the need for a scaled quantum chemical force field. This validated theoretical approach is essential in order to follow the formation of exfoliated clays and their surface reactivity that is experimentally unattainable.
Sorption of Pseudomonas putida onto differently structured kaolinite minerals
NASA Astrophysics Data System (ADS)
Vasiliadou, I. A.; Papoulis, D.; Chrysikopoulos, C.; Panagiotaras, D.; Karakosta, E.; Fardis, M.; Papavassiliou, G.
2010-12-01
The presence of bio-colloids (e.g. bacteria and viruses) in the subsurface could be attributed to the release of particles from septic tanks, broken sewer lines or from artificial recharge with treated municipal wastewater. Bio-colloid transport in the subsurface is significantly affected by sorption onto the solid matrix. Bio-colloid attachment onto mobile or suspended in the aqueous phase soil particles (e.g. clay or other minerals) also may influence their fate and transport in the subsurface. The present study focuses on the investigation of Pseudomonas (Ps.) putida sorption onto well (KGa-1) and poorly (KGa-2) crystallized kaolinite minerals. Batch experiments were carried out to determine the sorption isotherms of Ps. putida onto both types of kaolinite particles. The sorption process of Ps. putida onto KGa-1 and KGa-2 is adequately described by a Langmuir isotherm. Attenuated Total Reflection Fourier Transform Infrared Spectroscopy as well as Nuclear Magnetic Resonance were employed to study the sorption mechanisms of Ps. putida. Experimental results indicated that KGa-2 presented higher affinity and sorption capacity than KGa-1. It was shown that electrostatic interactions and structural disorders can influence the sorption capacity of clay particles.
NASA Astrophysics Data System (ADS)
Allard, T.; Fourdrin, C.; Calas, G.
2007-05-01
Understanding the processes controlling migrations of radioelements at the Earth's surface is an important issue for the long-term safety assessment of high level nuclear waste repositories (HLNWR). Evidence of past occurrence and transfer of radionuclides can be found using radiation-induced defects in minerals. Clay minerals are particularly relevant because of their widespread occurrence at the Earth's surface and their finely divided nature which provides high contact area with radioactive fluids. Owing to its sensitivity to radiations, kaolinite can be used as natural, in situ dosimeter. Kaolinite is known to contain radiation-induced defects which are detected by Electron Paramagnetic Resonance. They are differentiated by their nature, their production kinetics and their thermal stability. One of these defects is stable at the scale of geological periods and provides a record of past radionuclide occurrence. Based on artificial irradiations, a methodology has been subsequently proposed to determine paleodose cumulated by kaolinite since its formation. The paleodose can be used to derive equivalent radioelement concentrations, provided that the age of kaolinite formation can be constrained. This allows quantitative reconstruction of past transfers of radioelements in natural systems. An example is given for the Nopal I U-deposit (Chihuahua, Mexico), hosted in hydrothermally altered volcanic tufs and considered as analogue of the Yucca Mountain site. The paleodoses experienced by kaolinites were determined from the concentration of defects and dosimetry parameters of experimental irradiations. Using few geochemical assumption, a equivalent U-content responsible for defects in kaolinite was calculated from the paleodose, a dose rate balance and model ages of kaolinites constrained by tectonic phases. In a former study, the ages were assumptions derived from regional tectonic events. In thepresent study, ages of mineralization events are measured from U systematics. The corresponding results reveal past accumulation of uranium in the mineralized zone and past leaching in the fissure network of the present barren rock. Geochemical implications for HLNWR will be discussed.
Effect of pH and Electrolytes on Adsorption of 2,4-D onto Kaolinite
NASA Astrophysics Data System (ADS)
Sharma, A.; Kawamoto, K.; Komatsu, T.; Moldrup, P.
2006-12-01
The fate and transport of pesticides in soil can be greatly influenced by adsorption onto clay minerals such as kaolinite. The ionic pesticide 2,4-D (2,4-dichlorophenoxyacetic acid) is one of the most commonly used herbicides. The purpose of this study is to investigate the effect of electrolytes and pH on the adsorption of 2,4- D onto kaolinite. The adsorption coefficient (Kd) of 2,4-D on two types of kaolinite was measured in batch experiments using water and 4 different electrolytes (0.005M CaSO4, 0.005M CaCl2, 0.01M KCl, and 0.01M NaCl). The experiments were carried out with 0.5 g kaolinite at a solid:liquid ratio of 1:20 and at different pH (1.9-6.3). The pH of the solution was controlled by addition of 0.2N of HCl. X-ray diffraction analysis of both kaolinite with and without adsorbed 2,4-D was also done to understand the location of 2,4-D adsorption. The effects of pH and electrolytes on Kd were compared and possible adsorption mechanisms were revealed for 2,4-D adsorption onto the two different types of kaolinite. The results implied that 2,4-D adsorption was higher for an electrolyte solution with monovalent cation than with divalent cation for one type of kaolinite, while no such trend was observed for the other kaolinite. The adsorption of 2,4-D increased significantly with decreasing pH for both types of kaolinite.
Revision of Hopewellian trading patterns in Midwestern North America based on mineralogical sourcing
Hughes, R.E.; Berres, T.E.; Moore, D.M.; Farnsworth, K.B.
1998-01-01
Traditional exchange models purport that all Hopewell-style platform pipes of flint clay were quarried and crafted in southern Ohio by Native Americans from a local kaolinitic flint clay, and that those found in the Havana Hopewell region of western Illinois were transported from southern Ohio along an Ohio River trade network. However, the results of this study show that berthierine-rich flint clay from northwestern Illinois was the only source for pipestone artifacts of the Havana Hopewell region. We base this on (1) X-ray diffraction analysis of quickly made smears, (2) spatiotemporal distribution of artifacts in the Sterling-Rock Falls, Illinois area, and (3) petrographic, X-ray fluorescence, Mo??ssbauer, and SEM/EDX analyses. This understanding of the source of this material made it possible to visually identify the source of large numbers of curated artifacts as having been made of material from the Sterling-Rock Falls area. This discovery has implications for understanding cultural and material exchange among Hopewellian societies. Also, it is the first report of berthierine flint clay and of flint clay that formed before the evolution of terrestrial plants. ?? 1998 John Wiley & Sons, Inc.
NASA Astrophysics Data System (ADS)
Li, Jingrui; Liu, Shengfa; Shi, Xuefa; Feng, Xiuli; Fang, Xisheng; Cao, Peng; Sun, Xingquan; Wenxing, Ye; Khokiattiwong, Somkiat; Kornkanitnan, Narumol
2017-08-01
The clay mineral contents in 110 surface sediment samples collected from the middle of the Bay of Bengal were analyzed by X-ray diffraction (XRD) to investigate the provenance and transport patterns. The illite content was highest, followed by chlorite, kaolinite and then smectite, with average weight percent distributions of 52%, 22%, 14% and 12%, respectively. Illite and chlorite had similar distribution pattern, with higher contents in the northern and central areas and lower contents in the southern area, whereas smectite showed the opposite distribution pattern. Kaolinite show no obvious higher or lower areas and the southern ;belt; was one of the highest content areas. Based on the spatial distribution characteristics and cluster analysis results, the study area can be classified into two provinces. Province I covers the southwestern area and contains high concentrations of illite and smectite sediments. Province II covers most sites and is also characterized by high concentrations of illite, but the weight percent of smectite is only half of that of province I. According to a quantitative estimate using end-member clay minerals contents, the relative contributions from the Himalayan source and the Indian source are 63% and 37% on average, respectively. Integrative analysis indicates that the hydrodynamic environment in the study area, especially the turbidity and surface monsoonal circulation, plays an important role in the spatial distribution and dispersal of the clay fraction in the sediments. The sediments in province I are mainly from the Indian source transported by the East Indian Coastal Current (EICC) and the surface monsoon circulation with minor contributions from the Himalayan source while the sediments in province II are mainly from the Himalayan source transported by turbidity and surface monsoonal circulation with little contribution from Indian river materials.
Paragenesis and reservoir quality within a shallow combination trap: Central West Virginia
DOE Office of Scientific and Technical Information (OSTI.GOV)
Bell, D.A.; Siegrist, H.G. Jr.; Buurman, J.D.
1993-12-01
Sandstone character and reservoir quality of the Lower Mississippian Pocono Big Injun sandstone were examined in Granny Creek-Stockly field, Clay County, West Virginia. Sixty-three samples from 6 wells were analyzed using transmitted light, x-ray diffraction, and scanning electron microscopy techniques. The Pocono Big Injun formation is divided into four [open quotes]sands[close quotes] (Injun 1 through 4) based on composition and hydrocarbon productivity. The Injun 1 sand is a fine-grained, carbonate-cemented litharenite below the oil-producing zone. The oil-productive Injun 2 and 3 sands are well sorted, fine-grained litharenites which contain more authigenic and allogenic clay minerals than adjacent sands. These sandsmore » have produced more than 3.4 million bbl of oil from the Granny Creek part of the field since 1925. The Injun 4 sand is generally a coarse-grained sublitharenite with marginal gas production limited to the uppermost section of the sand. The paragenetic sequence consists of (1) minor quartz overgrowths, (2) illite and chlorite grain coatings, (3) quartz overgrowths, (4) early carbonate, (5) kaolinite, (6) calcite, (7) dolomite, and (8) pyrite. Porosity and permeability were not preserved once paragenesis progressed past the kaolinite stage. Porosity and permeability are variably preserved when steps in the paragenetic sequence are absent within the Pocono Group. Where any porosity is identified within the Pocono sandstones, primary porosity is dominant. However, secondary porosity and microporosity in clay-rich intervals are also important.« less
Alteration minerals in impact-generated hydrothermal systems - Exploring host rock variability
NASA Astrophysics Data System (ADS)
Schwenzer, Susanne P.; Kring, David A.
2013-09-01
Impact-generated hydrothermal systems have been previously linked to the alteration of Mars’ crust and the production of secondary mineral assemblages seen from orbit. The sensitivity of the resultant assemblages has not yet been evaluated as a function of precursor primary rock compositions. In this work, we use thermochemical modeling to explore the variety of minerals that could be produced by altering several known lithologies based on martian meteorite compositions. For a basaltic host rock lithology (Dhofar 378, Humphrey) the main alteration phases are feldspar, zeolite, pyroxene, chlorite, clay (nontronite, kaolinite), and hematite; for a lherzolithic host rock lithology (LEW 88516) the main alteration phases are amphibole, serpentine, chlorite, clay (nontronite, kaolinite), and hematite; and for an ultramafic host rock lithology (Chassigny) the main minerals are secondary olivine, serpentine, magnetite, quartz, and hematite. These assemblages and proportions of phases in each of those cases depend on W/R and temperature. Integrating geologic, hydrologic and alteration mineral evidence, we have developed a model to illustrate the distribution of alteration assemblages that occur in different levels of an impact structure. At the surface, hot, hydrous alteration affects the ejecta and melt sheet producing clay and chlorite. Deeper in the subsurface and depending on the permeability of the rock, a variety of minerals - smectite, chlorite, serpentine, amphiboles and hematite - are produced in a circulating hydrothermal system. These modeled mineral distributions should assist with interpretation of orbital observations and help guide surface exploration by rovers and sample return assets.
NASA Astrophysics Data System (ADS)
Won, Changdok; Hong, Hanlie; Cheng, Feng; Fang, Qian; Wang, Chaowen; Zhao, Lulu; Churchman, Gordon Jock
2018-03-01
To understand climate changes recorded in the Luochuan loess-palaeosols, Shaanxi province, northwestern China, clay mineralogy was studied using X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), and scanning electron microscopy (SEM) methods. XRD results show that clay mineral compositions in the Luochuan loess-palaeosols are dominantly illite, with minor chlorite, kaolinite, smectite, and illite-smectite mixed-layer clays (I/S). Illite is the most abundant species in the sediments, with a content of 61%-83%. The content of chlorite ranges from 5%-22%, and the content of kaolinite ranges from 5%-19%. Smectite (or I/S) occurs discontinuously along the loess profile, with a content of 0-8%. The Kübler index of illite (IC) ranges from 0.255°-0.491°, and the illite chemical index (ICI) ranges from 0.294-0.394. The CIA values of the loesspalaeosols are 61.9-69.02, and the R3+/(R3+ + R2+ + M+) values are 0.508-0.589. HRTEM observations show that transformation of illite to illite-smectite has occurred in both the loess and palaeosol, suggesting that the Luochuan loess-palaeosols have experienced a certain degree of chemical weathering. The Luochuan loess-palaeosols have the same clay mineral assemblage along the profile. However, the relative contents of clay mineral species, CIA, ICI, and IC values fluctuate frequently along the profile, and all these parameters display a similar trend. Moreover, climate changes suggested by the clay index are consistent with variations in the deep-sea δ18O records and the magnetic susceptibility value, and thus, climate changes in the Luochuan region have been controlled by global climate change.
NASA Technical Reports Server (NTRS)
Coyne, L. M.; Mariner, R.; Rice, A.
1991-01-01
Clay minerals have been shown to have numerous, curious, energetic properties by virtue of ultra-violet light release which can be triggered by gentle environmental changes such as wetting and dewetting by a variety of liquids, unique among them water and hydrazine. Since both water and hydrazine play multiple key roles in the air-oxidation of hydrazine on kaolinite surfaces, this reaction would seem to have prime potential for studying interrelationships of energy storage, release and chemical reactivity of clay surfaces, capacities basic to either the Bernal or Cairns-Smith roles of minerals in the origin of life. Establishment of the capacity for stored electronic energy to significantly alter surface chemistry is important, regardless of the reaction chosen to demonstrate it. Hydrazine air oxidation is overawingly complex, given the possibilities for step-wise control and monitoring of parameters. In the light of recently extended characterization of the kaolinite and model sheet catalysts we used to study hydrazine oxidation and gamma-irradiated silica, previous studies of hydrazine air-oxidation on aluminosilicate surfaces have been reevaluated. Our former conclusion remains intact that, whereas trace structural and surface contaminants do play some role in the catalysis of oxidation, they are not the only, nor even the dominant, catalytic centers. Initial intermediates in the oxidation can now be proposed which are consistent with production via O(-)-centers as well as ferric iron centers. The greater than square dependence of the initial reaction rate on the weight of the clay is discussed in the light of these various mechanistic possibilities.
Bacillus subtilis biofilm development in the presence of soil clay minerals and iron oxides.
Ma, Wenting; Peng, Donghai; Walker, Sharon L; Cao, Bin; Gao, Chun-Hui; Huang, Qiaoyun; Cai, Peng
2017-01-01
Clay minerals and metal oxides, as important parts of the soil matrix, play crucial roles in the development of microbial communities. However, the mechanism underlying such a process, particularly on the formation of soil biofilm, remains poorly understood. Here, we investigated the effects of montmorillonite, kaolinite, and goethite on the biofilm formation of the representative soil bacteria Bacillus subtilis . The bacterial biofilm formation in goethite was found to be impaired in the initial 24 h but burst at 48 h in the liquid-air interface. Confocal laser scanning microscopy showed that the biofilm biomass in goethite was 3-16 times that of the control, montmorillonite, and kaolinite at 48 h. Live/Dead staining showed that cells had the highest death rate of 60% after 4 h of contact with goethite, followed by kaolinite and montmorillonite. Atomic force microscopy showed that the interaction between goethite and bacteria may injure bacterial cells by puncturing cell wall, leading to the swarming of bacteria toward the liquid-air interface. Additionally, the expressions of abrB and sinR , key players in regulating the biofilm formation, were upregulated at 24 h and downregulated at 48 h in goethite, indicating the initial adaptation of the cells to minerals. A model was proposed to describe the effects of goethite on the biofilm formation. Our findings may facilitate a better understanding of the roles of soil clays in biofilm development and the manipulation of bacterial compositions through controlling the biofilm in soils.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Maher, K.; Steefel, C. I.; White, A.F.
2009-02-25
In order to explore the reasons for the apparent discrepancy between laboratory and field weathering rates and to determine the extent to which weathering rates are controlled by the approach to thermodynamic equilibrium, secondary mineral precipitation and flow rates, a multicomponent reactive transport model (CrunchFlow) was used to interpret soil profile development and mineral precipitation and dissolution rates at the 226 ka marine terrace chronosequence near Santa Cruz, CA. Aqueous compositions, fluid chemistry, transport, and mineral abundances are well characterized (White et al., 2008, GCA) and were used to constrain the reaction rates for the weathering and precipitating minerals inmore » the reactive transport modeling. When primary mineral weathering rates are calculated with either of two experimentally determined rate constants, the nonlinear, parallel rate law formulation of Hellmann and Tisser and [2006] or the aluminum inhibition model proposed by Oelkers et al. [1994], modeling results are consistent with field-scale observations when independently constrained clay precipitation rates are accounted for. Experimental and field rates, therefore, can be reconciled at the Santa Cruz site. Observed maximum clay abundances in the argillic horizons occur at the depth and time where the reaction fronts of the primary minerals overlap. The modeling indicates that the argillic horizon at Santa Cruz can be explained almost entirely by weathering of primary minerals and in situ clay precipitation accompanied by undersaturation of kaolinite at the top of the profile. The rate constant for kaolinite precipitation was also determined based on model simulations of mineral abundances and dissolved Al, SiO{sub 2}(aq) and pH in pore waters. Changes in the rate of kaolinite precipitation or the flow rate do not affect the gradient of the primary mineral weathering profiles, but instead control the rate of propagation of the primary mineral weathering fronts and thus total mass removed from the weathering profile. Our analysis suggests that secondary clay precipitation is as important as aqueous transport in governing the amount of dissolution that occurs within a profile because clay minerals exert a strong control over the reaction affinity of the dissolving primary minerals. The modeling also indicates that the weathering advance rate and the total mass of mineral dissolved is controlled by the thermodynamic saturation of the primary dissolving phases plagioclase and K-feldspar, as is evident from the difference in propagation rates of the reaction fronts for the two minerals despite their very similar kinetic rate laws.« less
Clay mineral type effect on bacterial enteropathogen survival in soil.
Brennan, Fiona P; Moynihan, Emma; Griffiths, Bryan S; Hillier, Stephen; Owen, Jason; Pendlowski, Helen; Avery, Lisa M
2014-01-15
Enteropathogens released into the environment can represent a serious risk to public health. Soil clay content has long been known to have an important effect on enteropathogen survival in soil, generally enhancing survival. However, clay mineral composition in soils varies, and different clay minerals have specific physiochemical properties that would be expected to impact differentially on survival. This work investigated the effect of clay materials, with a predominance of a particular mineral type (montmorillonite, kaolinite, or illite), on the survival in soil microcosms over 96 days of Listeria monocytogenes, Salmonella Dublin, and Escherichia coli O157. Clay mineral addition was found to alter a number of physicochemical parameters in soil, including cation exchange capacity and surface area, and this was specific to the mineral type. Clay mineral addition enhanced enteropathogen survival in soil. The type of clay mineral was found to differentially affect enteropathogen survival and the effect was enteropathogen-specific. © 2013.
The effect of switchable water additives on clay settling.
Chen, Chien-Shun; Lau, Ying Yin; Mercer, Sean M; Robert, Tobias; Horton, J Hugh; Jessop, Philip G
2013-01-01
The recycling of process water from strip mining extractions is a very relevant task both industrially and environmentally. The sedimentation of fine tailings during such processes, however, can often require long periods of time and/or the addition of flocculants which make later water recycling difficult. We propose the use of switchable water additives as reversible flocculants for clay/water suspensions. Switchable water additives are compounds such as diamines that make it possible to reversibly control the ionic strength of an aqueous solution. Addition of CO(2) to such an aqueous solution causes the ionic strength to rise dramatically, and the change is reversed upon removal of the CO(2). These additives, while in the presence of CO(2), promote the aggregation of clay tailings, reduce settling times, and greatly increase the clarity of the liberated water. The removal of CO(2) from the liberated water regenerates a low ionic strength solution that does not promote clay aggregation and settling until CO(2) is added again. Such reversible behavior would be useful in applications such as oil sands separations in which the recycled water must not promote aggregation. When added to kaolinite and montmorillonite clay suspensions, switchable water provided process waters of lower turbidity than those additives from inorganic salts or by CO(2)-treatment alone. When recollected, the switchable water supernatant was shown to be recyclable over three cycles for enhanced settling of kaolinite. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Testing the stability of magnetic iron oxides/kaolinite nanocomposite under various pH conditions
NASA Astrophysics Data System (ADS)
Tokarčíková, Michaela; Tokarský, Jonáš; Kutláková, Kateřina Mamulová; Seidlerová, Jana
2017-09-01
Magnetically modified clays containing iron oxides nanoparticles (FexOy NPs) are low-cost and environmentally harmless materials suitable for sorption of pollutants from wastewaters. Stability of this smart material was evaluated both experimentally and theoretically using molecular modelling. Original kaolinite and prepared FexOy/kaolinite nanocomposite were characterized using X-ray fluorescence spectroscopy, X-ray powder diffraction, infrared spectroscopy, and transmission electron microscopy, and the stability was studied using leaching tests performed according to the European technical standard EN 12457-2 in deionized water and extraction agents with varying pH (2, 4, 9, and 11). The influence of pH on amount of FexOy NPs released from the composite and amount of the basic elements released from the kaolinite structure was studied using inductively coupled plasma atomic emission spectroscopy. All experiments proved that the magnetic properties of the nanocomposite will not change even after leaching in extraction agents with various pH.
Antibacterial kaolinite/urea/chlorhexidine nanocomposites: Experiment and molecular modelling
NASA Astrophysics Data System (ADS)
Holešová, Sylva; Valášková, Marta; Hlaváč, Dominik; Madejová, Jana; Samlíková, Magda; Tokarský, Jonáš; Pazdziora, Erich
2014-06-01
Clay minerals are commonly used materials in pharmaceutical production both as inorganic carriers or active agents. The purpose of this study is the preparation and characterization of clay/antibacterial drug hybrids which can be further included in drug delivery systems for treatment oral infections. Novel nanocomposites with antibacterial properties were successfully prepared by ion exchange reaction from two types of kaolinite/urea intercalates and chlorhexidine diacetate. Intercalation compounds of kaolinite were prepared by reaction with solid urea in the absence of solvents (dry method) as well as with urea aqueous solution (wet method). The antibacterial activity of two prepared samples against Enterococcus faecalis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa was evaluated by finding the minimum inhibitory concentration (MIC). Antibacterial studies of both samples showed the lowest MIC values (0.01%, w/v) after 1 day against E. faecalis, E. coli and S. aureus. A slightly worse antibacterial activity was observed against P. aeruginosa (MIC 0.12%, w/v) after 1 day. Since samples showed very good antibacterial activity, especially after 1 day of action, this means that these samples can be used as long-acting antibacterial materials. Prepared samples were characterized by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The experimental data are supported by results of molecular modelling.
Effect of organic matter on CO(2) hydrate phase equilibrium in phyllosilicate suspensions.
Park, Taehyung; Kyung, Daeseung; Lee, Woojin
2014-06-17
In this study, we examined various CO2 hydrate phase equilibria under diverse, heterogeneous conditions, to provide basic knowledge for successful ocean CO2 sequestration in offshore marine sediments. We investigated the effect of geochemical factors on CO2 hydrate phase equilibrium. The three-phase (liquid-hydrate-vapor) equilibrium of CO2 hydrate in the presence of (i) organic matter (glycine, glucose, and urea), (ii) phyllosilicates [illite, kaolinite, and Na-montmorillonite (Na-MMT)], and (iii) mixtures of them was measured in the ranges of 274.5-277.0 K and 14-22 bar. Organic matter inhibited the phase equilibrium of CO2 hydrate by association with water molecules. The inhibition effect decreased in the order: urea < glycine < glucose. Illite and kaolinite (unexpandable clays) barely affected the CO2 hydrate phase equilibrium, while Na-MMT (expandable clay) affected the phase equilibrium because of its interlayer cations. The CO2 hydrate equilibrium conditions, in the illite and kaolinite suspensions with organic matter, were very similar to those in the aqueous organic matter solutions. However, the equilibrium condition in the Na-MMT suspension with organic matter changed because of reduction of its inhibition effect by intercalated organic matter associated with cations in the Na-MMT interlayer.
NASA Astrophysics Data System (ADS)
Varol, Baki; Koşun, Erdal; Ünal Pinar, Neslihan; Ayranci, Korhan
2011-03-01
This paper is the first study of pyritized mudstones (PM) in the Permian-Triassic (P-T) boundary section of the Çürük Dağ (Taurus, Antalya Nappes, Turkey). The mudstones were generally formed as lensoidal-shaped layers or infill materials within nodular platform limestones (hardground). Normal marine fauna is diminished in the pyritized limestones, whereas tube-like microorganisms are apparently increased with the association of pyrite crystals consisting of both framboidal and cubic crystals. The total rock volumes are up to 50-60% clay minerals and are mainly made up of in situ kaolinite and subordinate mixed layer clays (illite-vermiculite). Kaolinite preferentially developed on feldspar crystals, sometimes covering ostracoda bivalves together with gypsum micronodules composed of fan-shaped gypsum crystals. The origin of the kaolinite is, in situ, directly related to feldspar dissolution via heterotrophic bacteria. Thus, kaolinite is found along with bacterial structures. Other mineralogical compositions include established quartz (mostly β-quartz), gypsum crystals (100-200 μm) glauconite and magnetite. Magnetite grains comprise a minor amount (1-2%) and show some bacterial-induced crystal orientations. Glauconite is formed as an accessory mineral that occurs as infill material in biogenic grains. On the other hand, some microspheres represented by a silica-dominated composition are only observed in scanning electron microscopes (SEM) studies under high magnification. Isotope values (d34S) obtained from the pyritized mudstones show an isotopic heterogeneity that suggests that the pyritized mudstone consists of at least two components, with different sulphur-concentrations and d34S values.
Dedzo, Gustave K; Ngnie, Gaëlle; Detellier, Christian
2016-02-01
The synthesis of selectively deposited palladium nanoparticles (PdNPs) inside tubular halloysite lumens is reported. This specific localization was directed by the selective modification of the aluminol surfaces of the clay mineral through stable Al-O-C bonds. An ionic liquid (1-(2-hydroxyethyl)-3-methylimidazolium) was grafted onto halloysite following the guest displacement method (generally used for kaolinite) using halloysite-DMSO preintercalate. The characterization of this clay nanohybrid material (XRD, NMR, TGA) showed characteristics reminiscent of similar materials synthesized from kaolinite. The grafting on halloysite lumens was also effective without using the DMSO preintercalate. The presence of these new functionalities in halloysite directs the synthesis of uniform PdNPs with size ranging between 3 and 6 nm located exclusively in the lumens. This results from the selective adsorption of PdNPs precursors in functionalized lumens through an anion exchange mechanism followed by in situ reduction. In contrast, the unmodified clay mineral displayed nanoparticles both inside and outside the tubes. These catalysts showed significant catalytic activity for the reduction of 4-nitrophenol (4-NP). The most efficient catalysts were recycled up to three times without reducing significantly the catalytic activities.
One-dimensional pore pressure diffusion of different grain-fluid mixtures
NASA Astrophysics Data System (ADS)
von der Thannen, Magdalena; Kaitna, Roland
2015-04-01
During the release and the flow of fully saturated debris, non-hydrostatic fluid pressure can build up and probably dissipate during the event. This excess fluid pressure has a strong influence on the flow and deposition behaviour of debris flows. Therefore, we investigate the influence of mixture composition on the dissipation of non-hydrostatic fluid pressures. For this we use a cylindrical pipe of acrylic glass with installed pore water pressure sensors in different heights and measure the evolution of the pore water pressure over time. Several mixtures with variable content of fine sediment (silt and clay) and variable content of coarse sediment (with fixed relative fractions of grains between 2 and 32 mm) are tested. For the fines two types of clay (smectite and kaolinite) and loam (Stoober Lehm) are used. The analysis is based on the one-dimensional consolidation theory which uses a diffusion coefficient D to model the decay of excess fluid pressure over time. Starting from artificially induced super-hydrostatic fluid pressures, we find dissipation coefficients ranging from 10-5 m²/s for liquid mixtures to 10-8 m²/s for viscous mixtures. The results for kaolinite and smectite are quite similar. For our limited number of mixtures the effect of fines content is more pronounced than the effect of different amounts of coarse particles.
NASA Astrophysics Data System (ADS)
Orhan, Hükmü
1992-04-01
The importance of dust storms on geological processes has only been studied recently. Case-hardening, desert-varnish formation, duricrust development, reddening and cementation of sediments and caliche formation, are some important geological processes related to dust storms. Dust storms can also be a major source for cements in aeolian sandstones. The Jurassic aeolian Entrada Formation in the Ghost Ranch area is composed of quartz with minor amounts of feldspar and rock fragments, and is cemented with smectite as grain coatings and calcite and kaolinite as pore fillings. Smectite shows a crinkly and honeycomb-like morphology which points to an authigenic origin. The absence of smectite as framework grains and the presence of partially dissolved grains, coated with smectite and smectite egg-shells, indicate an external source. Clay and fine silt-size particles are believed to be the major source for cements, smectite and calcite in the Entrada Formation. The common association of kaolinite with altered feldspar, and the absence of kaolinite in spots heavily cemented with calcite, lead to the conclusions that the kaolinite formation postdates carbonates and that framework feldspar grains were the source of kaolinite.
Clay mineralogy in different geomorphic surfaces in sugarcane areas
NASA Astrophysics Data System (ADS)
Camargo, L.; Marques, J., Jr.
2012-04-01
The crystallization of the oxides and hydroxides of iron and aluminum and kaolinite of clay fraction is the result of pedogenetic processes controlled by the relief. These minerals have influence on the physical and chemical attributes of soil and exhibit spatial dependence. The pattern of spatial distribution is influenced by forms of relief as the geomorphic surfaces. In this sense, the studies aimed at understanding the relationship between relief and the distribution pattern of the clay fraction attributes contribute to the delineation of specific areas of management in the field. The objective of this study was to evaluate the spatial distribution of oxides and hydroxides of iron and aluminum and kaolinite of clay fraction and its relationship with the physical and chemical attributes in different geomorphic surfaces. Soil samples were collected in a transect each 25 m (100 samples) and in the sides of the same (200 samples) as well as an area of 500 ha (1 sample each six hectare). Geomorphic surfaces (GS) in the transect were mapped in detail to support mapping the entire area. The soil samples were taken to the laboratory for chemical, physical, and mineralogical analysis, and the pattern of spatial distribution of soil attributes was obtained by statistics and geostatistics. The GS I is considered the oldest surface of the study area, with depositional character, and a slope ranging from 0 to 4%. GS II and III are considered to be eroded, and the surface II plan a gentle slope that extends from the edge of the surface until the beginning of I and III. The crystallographic characteristics of the oxides and hydroxides of iron and aluminum and kaolinite showed spatial dependence and the distribution pattern corresponding to the limits present of the GS in the field. Surfaces I and II showed the best environments to the degree of crystallinity of hematite and the surface III to the greatest degree of crystallinity of goethite agreeing to the pedoenvironment conditions of each surface. The rate goethite/(goethite+hematite) decreases the surface I to III this result is the variation of the source material that has an increase of clay which is characteristic of sandstone rock (Adamantine Formation) in the surface III. The rate kaolinite/(kaolinite+gibbsite) also shows a decrease of the surface I to the surface III. The spatial distribution pattern of mineralogy influenced the pattern of physical and chemical properties. On the surface III (with higher iron and gibbsite) had the best physical condition (lower density, higher porosity and aggregates) and greater phosphorus sorption. In this sense, the identification and mapping of the GSs, allowed a better understanding of cause and effect of the distribution of soils in the area, and the recognition of areas of controlled variability of soil attributes. These areas can be considered specific areas of management, useful for planning and management practices in the culture of sugarcane. Besides, suggesting criteria for the recognition of map units that would be equivalent to the future series of soils of the Brazilian System of Soil Classification.
CLAY, COASTAL REGIONS, CYCLES, DELTAS, DEPOSITION, DIAGNOSIS(GENERAL), FINES, FLOW, GEOLOGY, GEOMORPHOLOGY, KAOLINITE , MATHEMATICAL MODELS, MINERALS...MODELS, MONTMORILLONITE , PARAMETERS, PETROGRAPHY, PROCESSING, RATIOS, RESIDUALS, RESPONSE, RIVERS, SALINITY, SAMPLING, SAND, SCHIST, SEDIMENTS
Holocene debris flows on the Colorado Plateau: The influence of clay mineralogy and chemistry
Webb, R.H.; Griffiths, P.G.; Rudd, L.P.
2008-01-01
Holocene debris flows do not occur uniformly on the Colorado Plateau province of North America. Debris flows occur in specific areas of the plateau, resulting in general from the combination of steep topography, intense convective precipitation, abundant poorly sorted material not stabilized by vegetation, and the exposure of certain fine-grained bedrock units in cliffs or in colluvium beneath those cliffs. In Grand and Cataract Canyons, fine-grained bedrock that produces debris flows contains primarily single-layer clays - notably illite and kaolinite - and has low multilayer clay content. This clay-mineral suite also occurs in the colluvium that produces debris flows as well as in debris-flow deposits, although unconsolidated deposits have less illite than the source bedrock. We investigate the relation between the clay mineralogy and major-cation chemistry of fine-grained bedrock units and the occurrence of debris flows on the entire Colorado Plateau. We determined that 85 mapped fine-grained bedrock units potentially could produce debris flows, and we analyzed clay mineralogy and major-cation concentration of 52 of the most widely distributed units, particularly those exposed in steep topography. Fine-grained bedrock units that produce debris flows contained an average of 71% kaolinite and illite and 5% montmorillonite and have a higher concentration of potassium and magnesium than nonproducing units, which have an average of 51% montmorillonite and a higher concentration of sodium. We used multivariate statistics to discriminate fine-grained bedrock units with the potential to produce debris flows, and we used digital-elevation models and mapped distribution of debris-flow producing units to derive a map that predicts potential occurrence of Holocene debris flows on the Colorado Plateau. ?? 2008 Geological Society of America.
NASA Astrophysics Data System (ADS)
Verma, Kamlesh; Bhattacharya, Sanjeeb; Biswas, P.; Shrivastava, Prakash K.; Pandey, Mayuri; Pant, N. C.
2014-11-01
Core U1359 collected from the continental rise off Wilkes Land, east Antarctica, is analyzed for the clay mineralogy and carbon content. The temporal variation of the clay mineralogical data shows a dominance of illite with chlorite, smectite and kaolinite in decreasing concentration. Clay mineral illite is negatively correlated with smectite which shows enrichment during 6.2-6.8, 5.5-5.8, 4.5 and 2.5 Ma. The mineralogical analyses on the silt size fraction (2-53 μm) of some selected samples were also carried out. The combined result of both the size fractions shows the presence of chlorite and illite in both size fractions, smectite and kaolinite only in clay size fraction (<2 μm) and similarity in the crystallinity and chemistry of illite in both fractions. Similar nature of illite in both fractions suggests negligible role of sorting probably due to the deposition from the waxing ice sheet. During times of ice growth, nearby cratonic east Antarctica shield provided biotite-rich sediments to the depositional site. On the other hand, the presence of smectite, only in the clay size fraction, suggests the effective role of sorting probably due to the deposition from distal source in ice retreat condition. During times of ice retreat, smectite-rich sediment derived from Ross Orogen is transported to the core site through surface or bottom water currents. Poor crystallinity of illite due to degradation further corroborates the ice retreat condition. The ice sheet proximal sediments of U1359 show that in the eastern part of Wilkes Land, the `warming' was initiated during late Miocene.
NASA Astrophysics Data System (ADS)
Fleury, Guillaume; Del Nero, Mirella; Barillon, Rémi
2017-01-01
We addressed the effects of mineral surface properties (kaolinite versus Al-oxide) on the sorption-driven fractionation of a soil fulvic acid (FA) at acidic pH, mainly by means of ESI(-)-FTMS analysis of initial and supernatant solutions of FA sorption batch experiments. The MS data provided clear molecular-scale evidence of distinct mechanisms and molecular parameters controlling the FA fractionation upon its sorption on clay and oxide surfaces, respectively. Identification of sorbing and not-sorbing FA compounds in kaolinite-solution systems revealed a weak fractionation among members of sbnd CO2 series of aliphatics or not-condensed aromatics (NCAs) at pH 3.8, and almost no sorption of poorly-oxygenated polycyclic aromatic compounds (PACs) and NCAs. This first molecular-scale description of a FA fractionation in a clay-solution system suggests that H-bonding with low affinity sites (aluminol/silanol) on the basal planes of the clay particles is the main mechanism of sorption. Due to the predominance of such weak and poorly-selective mechanism, the sorption of aliphatic and NCA molecules bearing oxygenated functionalities was prevented at pH 5, due to dissolved Al competing successfully for their coordination. In contrast, a strong FA fractionation was observed onto alumina, with a preferential retention of PACs and highly-oxygenated aliphatics and NCAs. The major part of the poorly oxygenated aliphatics was left in solution. The sorption degree of NCAs and aliphatics was strongly correlated with molecular acidity. For PACs and poorly-oxygenated NCAs, the sorption was driven by reactions of surface ligand exchange (for the most oxygenated compounds) or by hydrophobic interactions (for the least oxygenated compounds).
Heavy metals alter the electrokinetic properties of bacteria, yeasts, and clay minerals.
Collins, Y E; Stotzky, G
1992-01-01
The electrokinetic patterns of four bacterial species (Bacillus subtilis, Bacillus megaterium, Pseudomonas aeruginosa, and Agrobacterium radiobacter), two yeasts (Saccharomyces cerevisiae and Candida albicans), and two clay minerals (montmorillonite and kaolinite) in the presence of the chloride salts of the heavy metals, Cd, Cr, Cu, Hg, Ni, Pb, and Zn, and of Na and Mg were determined by microelectrophoresis. The cells and kaolinite were net negatively charged at pH values above their isoelectric points (pI) in the presence of Na, Mg, Hg, and Pb at an ionic strength (mu) of 3 x 10(-4); montmorillonite has no pI and was net negatively charged at all pH values in the presence of these metals. However, the charge of some bacteria, S. cerevisiae, and kaolinite changed to a net positive charge (charge reversal) in the presence of Cd, Cr, Cu, Ni, and Zn at pH values above 5.0 (the pH at which charge reversal occurred differed with the metal) and then, at higher pH values, again became negative. The charge of the bacteria and S. cerevisiae also reversed in solutions of Cu and Ni with a mu of greater than 3 x 10(-4), whereas there was no reversal in solutions with a mu of less than 3 x 10(-4). The clays became net positively charged when the mu of Cu was greater than 3 x 10(-4) and that of Ni was greater than 1.5 x 10(-4). The charge of the cells and clays also reversed in solutions containing both Mg and Ni or both Cu and Ni (except montmorillonite) but not in solutions containing both Mg and Cu (except kaolinite) (mu = 3 x 10(-4)). The pIs of the cells in the presence of the heavy metals were at either higher or lower pH values than in the presence of Na and Mg. Exposure of the cells to the various metals at pH values from 2 to 9 for the short times (ca. 10 min) required to measure the electrophoretic mobility did not affect their viability. The specific adsorption on the cells and clays of the hydrolyzed species of some of the heavy metals that formed at higher pH values was probably responsible for the charge reversal. These results suggest that the toxicity of some heavy metals to microorganisms varies with pH because the hydrolyzed speciation forms of these metals, which occur at higher pH values, bind on the cell surface and alter the net charge of the cell.(ABSTRACT TRUNCATED AT 400 WORDS) PMID:1622229
Surface Complexation Modeling of U(VI) Adsorption onto Savannah River Site Sediments
NASA Astrophysics Data System (ADS)
Dong, W.; Wan, J.; Tokunaga, T. K.; Denham, M.; Davis, J.; Hubbard, S. S.
2011-12-01
The Savannah River Site (SRS) was a U.S. Department of Energy facility for plutonium production during the Cold War. Waste plumes containing low-level radioactivity and acidic waste solutions were discharged to a series of unlined seepage basins in the F-Area of the SRS from 1955 to 1988. Although the site has undergone many years of active remediation, the groundwater remains acidic, and the concentrations of U and other radionuclides are still significantly higher than their Maximum Contaminant Levels (MCLs). The objective of this effort is to understand and predict U(VI) mobility in acidic waste plumes through developing surface complexation models (SCMs). Laboratory batch experiments were conducted to evaluate U adsorption behavior over the pH range of 3.0 to 9.5. Ten sorbent samples were selected including six contaminated sediment samples from three boreholes drilled within the plume and along the groundwater flow direction, two uncontaminated (pristine) sediment samples from a borehole outside of the plume, and two reference minerals, goethite and kaolinite (identified as the dominant minerals in the clay size fraction of the F-Area sediments). The results show that goethite and kaolinite largely control U partitioning behavior. In comparison with the pristine sediment, U(VI) adsorption onto contaminated sediments exhibits adsorption edges shifted toward lower pH by about 1.0 unit (e.g., from pH≈4.5 to pH≈3.5). We developed a SCMs based component additivity (CA) approach, which can successfully predict U(VI) adsorption onto uncontaminated SRS sediments. However, application of the same SCMs based CA approach to contaminated sediments resulted in underestimates of U(VI) adsorption at acidic pH conditions. The model sensitivity analyses indicate that both goethite and kaolinite surfaces co-contributed to U(VI) adsorption under acidic pH conditions. In particular, the exchange sites of clay minerals might play an important role in adsorption of U(VI) at pH < 5.0. These results suggested that the contaminated sediments might either contain other more reactive clay minerals such as smectite, or that the long-term acid-leaching process might have altered the surface reactivity of the original sediments. Further studies are needed to identify more reactive mineral facies and understand the effects of acid leaching on the surface reactivity of the sediments.
Interaction of human adenoviruses and coliphages with kaolinite and bentonite.
Bellou, Maria I; Syngouna, Vasiliki I; Tselepi, Maria A; Kokkinos, Petros A; Paparrodopoulos, Spyros C; Vantarakis, Apostolos; Chrysikopoulos, Constantinos V
2015-06-01
Human adenoviruses (hAdVs) are pathogenic viruses responsible for public health problems worldwide. They have also been used as viral indicators in environmental systems. Coliphages (e.g., MS2, ΦX174) have also been studied as indicators of viral pollution in fecally contaminated water. Our objective was to evaluate the distribution of three viral fecal indicators (hAdVs, MS2, and ΦΧ174), between two different phyllosilicate clays (kaolinite and bentonite) and the aqueous phase. A series of static and dynamic experiments were conducted under two different temperatures (4, 25°C) for a time period of seven days. HAdV adsorption was examined in DNase I reaction buffer (pH=7.6, and ionic strength (IS)=1.4mM), whereas coliphage adsorption in phosphate buffered saline solution (pH=7, IS=2mM). Moreover, the effect of IS on hAdV adsorption under static conditions was evaluated. The adsorption of hAdV was assessed by real-time PCR and its infectivity was tested by cultivation methods. The coliphages MS2 and ΦΧ174 were assayed by the double-layer overlay method. The experimental results have shown that coliphage adsorption onto both kaolinite and bentonite was higher for the dynamic than the static experiments; whereas hAdV adsorption was lower under dynamic conditions. The adsorption of hAdV increased with decreasing temperature, contrary to the results obtained for the coliphages. This study examines the combined effect of temperature, agitation, clay type, and IS on hAdV adsorption onto clays. The results provide useful new information on the effective removal of viral fecal indicators (MS2, ΦX174 and hAdV) from dilute aqueous solutions by adsorption onto kaolinite and bentonite. Factors enabling enteric viruses to penetrate soils, groundwater and travel long distances within aquifers are important public health issues. Because the observed adsorption behavior of surrogate coliphages MS2 and ΦΧ174 is substantially different to that of hAdV, neither MS2 nor ΦΧ174 is recommended as a suitable model for adenovirus. Copyright © 2015 Elsevier B.V. All rights reserved.
Hosterman, John W.; Flanagan, F.J.; Bragg, Anne; Doughten, M.W.; Filby, R.H.; Grimm, Catherine; Mee, J.S.; Potts, P.J.; Rogers, N.W.
1987-01-01
The concentrations of 3 oxides and 29 elements in 7 National Bureau of Standards (NBS) and 3 Instituto de Pesquisas Techno16gicas (IPT) reference clay samples were etermined by instrumental neutron activation analysis. The analytical work was designed to test the homogeneity of constituents in three new NBS reference clays, NBS-97b, NBS-98b, and NBS-679. The analyses of variance of 276 sets of data for these three standards show that the constituents are distributed homogeneously among bottles of samples for 94 percent of the sets of data. Three of the reference samples (NBS-97, NBS-97a, and NBS-97b) are flint clays; four of the samples (NBS-98, NBS-98a, NBS-98b, and IPT-32) are plastic clays, and three of the samples (NBS-679, IPT-28, and IPT-42) are miscellaneous clays (both sedimentary and residual). Seven clays are predominantly kaolinite; the other three clays contain illite and kaolinite in the approximate ratio 3:2. Seven clays contain quartz as the major nonclay mineral. The mineralogy of the flint and plastic clays from Missouri (NBS-97a and NBS-98a) differs markedly from that of the flint and plastic clays from Pennsylvania (NBS-97, NBS-97b, NBS-98, and NBS-98b). The flint clay NBS-97 has higher average chromium, hafnium, lithium, and zirconium contents than its replacement, reference sample NBS-97b. The differences between the plastic clay NBS-98 and its replacement, NBS-98b, are not as pronounced. The trace element contents of the flint and plastic clays from Missouri, NBS-97a and NBS-98a, differ significantly from those of the clays from Pennsylvania, especially the average rare earth element (REE) contents. The trace element contents of clay sample IPT-32 differ from those of the other plastic clays. IPT-28 and IPT-42 have some average trace element contents that differ not only between these two samples but also from all the other clays. IPT-28 has the highest summation of the average REE contents of the 10 samples. The uranium content of NBS-98a, 46 parts per million, is very much higher than that of the other clays. Plots of average REE contents of the flint and plastic clays, normalized to chondritic abundances, show that the clays from Missouri differ from the same types of clay from Pennsylvania. The plot of REE contents for the miscellaneous clays shows that the normalized means for the elements lanthanum through samarium for IPT-28 are much greater than those for the other miscellaneous clays. The means for the elements europium through lutetium are similar for all three miscellaneous clays.
Unraveling the antibacterial mode of action of a clay from the Colombian Amazon.
Londono, Sandra Carolina; Williams, Lynda B
2016-04-01
Natural antibacterial clays can inhibit growth of human pathogens; therefore, understanding the antibacterial mode of action may lead to new applications for health. The antibacterial modes of action have shown differences based on mineralogical constraints. Here we investigate a natural clay from the Colombian Amazon (AMZ) known to the Uitoto natives as a healing clay. The physical and chemical properties of the AMZ clay were compared to standard reference materials: smectite (SWy-1) and kaolinite (API #5) that represent the major minerals in AMZ. We tested model Gram-negative (Escherichia coli ATCC #25922) and Gram-positive (Bacillus subtilis ATCC #6633) bacteria to assess the clay's antibacterial effectiveness against different bacterial types. The chemical and physical changes in the microbes were examined using bioimaging and mass spectrometry of clay digests and aqueous leachates. Results indicate that a single dose of AMZ clay (250 mg/mL) induced a 4-6 order of magnitude reduction in cell viability, unlike the reference clays that did not impact bacterial survival. AMZ clay possesses a relatively high specific surface area (51.23 m(2)/g) and much higher total surface area (278.82 m(2)/g) than the reference clays. In aqueous suspensions (50 mg clay/mL water), soluble metals are released and the minerals buffer fluid pH between 4.1 and 4.5. We propose that the clay facilitates chemical interactions detrimental to bacteria by absorbing nutrients (e.g., Mg, P) and potentially supplying metals (e.g., Al) toxic to bacteria. This study demonstrates that native traditional knowledge can direct scientific studies.
Commercial demonstration of kaolinitic clay for protection of Flavobacterium columnaris in sportfish
USDA-ARS?s Scientific Manuscript database
Sportfish farms in Arkansas routinely battle Columnaris disease, which is caused by Flavobacterium columnare. Columnaris is especially prevalent during the feed training of centrarchids such as largemouth bass and immediately following harvest of crappie, redear sunfish, and bluegill while they are ...
A role for subducted super-hydrated kaolinite in Earth’s deep water cycle
DOE Office of Scientific and Technical Information (OSTI.GOV)
Hwang, Huijeong; Seoung, Donghoon; Lee, Yongjae
Water is the most abundant volatile component in the Earth. It continuously enters the mantle through subduction zones, where it reduces the melting temperature of rocks to generate magmas. The dehydration process in subduction zones, which determines whether water is released from the slab or transported into the deeper mantle, is an essential component of the deep water cycle. Here we use in situ and time-resolved high-pressure/high-temperature synchrotron X-ray diffraction and infrared spectra to characterize the structural and chemical changes of the clay mineral kaolinite. At conditions corresponding to a depth of about 75 km in a cold subducting slabmore » (2.7 GPa and 200 °C), and in the presence of water, we observe the pressure-induced insertion of water into kaolinite. This super-hydrated phase has a unit cell volume that is about 31% larger, a density that is about 8.4% lower than the original kaolinite and, with 29 wt% H2O, the highest water content of any known aluminosilicate mineral in the Earth. As pressure and temperature approach 19 GPa and about 800 °C, we observe the sequential breakdown of super-hydrated kaolinite. The formation and subsequent breakdown of super-hydrated kaolinite in cold slabs subducted below 200 km leads to the release of water that may affect seismicity and help fuel arc volcanism at the surface.« less
A role for subducted super-hydrated kaolinite in Earth's deep water cycle
NASA Astrophysics Data System (ADS)
Hwang, Huijeong; Seoung, Donghoon; Lee, Yongjae; Liu, Zhenxian; Liermann, Hanns-Peter; Cynn, Hyunchae; Vogt, Thomas; Kao, Chi-Chang; Mao, Ho-Kwang
2017-12-01
Water is the most abundant volatile component in the Earth. It continuously enters the mantle through subduction zones, where it reduces the melting temperature of rocks to generate magmas. The dehydration process in subduction zones, which determines whether water is released from the slab or transported into the deeper mantle, is an essential component of the deep water cycle. Here we use in situ and time-resolved high-pressure/high-temperature synchrotron X-ray diffraction and infrared spectra to characterize the structural and chemical changes of the clay mineral kaolinite. At conditions corresponding to a depth of about 75 km in a cold subducting slab (2.7 GPa and 200 °C), and in the presence of water, we observe the pressure-induced insertion of water into kaolinite. This super-hydrated phase has a unit cell volume that is about 31% larger, a density that is about 8.4% lower than the original kaolinite and, with 29 wt% H2O, the highest water content of any known aluminosilicate mineral in the Earth. As pressure and temperature approach 19 GPa and about 800 °C, we observe the sequential breakdown of super-hydrated kaolinite. The formation and subsequent breakdown of super-hydrated kaolinite in cold slabs subducted below 200 km leads to the release of water that may affect seismicity and help fuel arc volcanism at the surface.
Hyperspectral analysis of clay minerals
NASA Astrophysics Data System (ADS)
Janaki Rama Suresh, G.; Sreenivas, K.; Sivasamy, R.
2014-11-01
A study was carried out by collecting soil samples from parts of Gwalior and Shivpuri district, Madhya Pradesh in order to assess the dominant clay mineral of these soils using hyperspectral data, as 0.4 to 2.5 μm spectral range provides abundant and unique information about many important earth-surface minerals. Understanding the spectral response along with the soil chemical properties can provide important clues for retrieval of mineralogical soil properties. The soil samples were collected based on stratified random sampling approach and dominant clay minerals were identified through XRD analysis. The absorption feature parameters like depth, width, area and asymmetry of the absorption peaks were derived from spectral profile of soil samples through DISPEC tool. The derived absorption feature parameters were used as inputs for modelling the dominant soil clay mineral present in the unknown samples using Random forest approach which resulted in kappa accuracy of 0.795. Besides, an attempt was made to classify the Hyperion data using Spectral Angle Mapper (SAM) algorithm with an overall accuracy of 68.43 %. Results showed that kaolinite was the dominant mineral present in the soils followed by montmorillonite in the study area.
Negative grouting consequences on karst environment
NASA Astrophysics Data System (ADS)
Bonacci, O.; Roje-Bonacci, T.; Gottstein, S.
2009-04-01
Grouting is a procedure by means of which grout is injected into different kinds of karst spaces (cracks, fissures, conduits and caves). It has a wide application in modern civil engineering, especially in karst terrains. It started nearly 200 years ago. In most cases the ingredients for the preparation of mortars and grouting suspensions are: cement, bentonite, clay and fillers, additives for stability and water. In practice the composition of grouting suspension is not standardized. A suspension injected under pressure will circulate in the karst spaces like a more or less viscous fluid until some of the larger suspended particles are blocked where the karst voids get narrower than the size of injected grains. The injection of materials into karst groundwater, i.e. the construction of grouting curtains, definitely could be the cause of unpredictable negative consequences on karst groundwater environments. The building of dams in karst areas always go along the construction of grouting curtains. During the construction of most dams in karst all over the world millions tons of injection mass have been injected in karst underground. It may impact water quantity in vadose zone and in karstic aquifer causing water table lowering and spring desiccation. In such cases the negative impact on local karst environment could be very dangerous. Physically as well as chemically this mass voraciously and quickly destroyed underground habitats and killed an enormous number of endangered and endemic species. Very often this is extremely expensive procedure and in many cases not very successful from the engineering point of view. From the ecological point of view it could causes catastrophic consequences. The greatest problem is that until now neither engineers nor ecologists took care of these great and massive negative influences on underground karst environments. In this paper few examples of different consequences of grouting on the hydrogeological as well as ecological regime on karst environment in the Dinaric karst are given. The goal of this paper is to warn scientific community that is time to start with interdisciplinary research of this problem.
NASA Astrophysics Data System (ADS)
Crasto de Lima, F. D.; Miwa, R. H.; Miranda, Caetano R.
2017-11-01
Layered clay materials have been used to incorporate transition metal (TM) contaminants. Based on first-principles calculations, we have examined the energetic stability and the electronic properties due to the incorporation of Cd and Hg in layered clay materials, kaolinite (KAO) and pyrophyllite (PYR). The TM can be (i) adsorbed on the clay surface as well as (ii) intercalated between the clay layers. For the intercalated case, the contaminant incorporation rate can be optimized by controlling the interlayer spacing of the clay, namely, pillared clays. Our total energy results reveal that the incorporation of the TMs can be maximized through a suitable tuning of vertical distance between the clay layers. Based on the calculated TM/clay binding energies and the Langmuir absorption model, we estimate the concentrations of the TMs. Further kinetic properties have been examined by calculating the activation energies, where we found energy barriers of ˜20 and ˜130 meV for adsorbed and intercalated cases, respectively. The adsorption and intercalation of ionized TM adatoms were also considered within the deprotonated KAO surface. This also leads to an optimal interlayer distance which maximizes the TM incorporation rate. By mapping the total charge transfers at the TM/clay interface, we identify a net electronic charge transfer from the TM adatoms to the topmost clay surface layer. The effect of such a charge transfer on the electronic structure of the clay (host) has been examined through a set of X-ray absorption near edge structure (XANES) simulations, characterizing the changes of the XANES spectra upon the presence of the contaminants. Finally, for the pillared clays, we quantify the Cd and Hg K-edge energy shifts of the TMs as a function of the interlayer distance between the clay layers and the Al K-edge spectra for the pristine and pillared clays.
Removal of organic pollutants and heavy metals in soils by electrokinetic remediation.
Ricart, M T; Pazos, M; Gouveia, S; Cameselle, C; Sanroman, M A
2008-07-01
In this work, the feasibility of electrokinetic remediation for the restoration of polluted soil with organic and inorganic compounds had been development and evaluated using a model soil sample. The model soil was prepared with kaolinite clay artificially polluted in the laboratory with chromium and an azo dye: Reactive Black 5 (RB5). The electromigration of Cr in a spiked kaolinite sample was studied in alkaline conditions. Despite of the high pH registered in the kaolinite sample (around pH 9.5), Cr migrated towards the cathode and it was accumulated in the cathode chamber forming a white precipitate. The removal was not complete, and 23% of the initial Cr was retained into the kaolinite sample close to the cathode side. The azo dye RB5 could be effectively removed from kaolinite by electrokinetics and the complete cleanup of the kaolinite could be achieved in alkaline environment. In this condition, RB5 formed an anion that migrated towards the anode where it was accumulated and quickly degraded upon the electrode surface. The electrokinetic treatment of a kaolinite sample polluted with both Cr and RB5 yielded very good results. The removal of Cr was improved compared to the experiment where Cr was the only pollutant, and RB5 reached a removal as high as 95%. RB5 was removed by electromigration towards the anode, where the dye was degraded upon the surface of the electrode by electrochemical oxidation. Cr was transported towards the cathode by electromigration and electroosmosis. It is supposed that the interaction among RB5 and Cr into the kaolinite sample prevented premature precipitation and allow Cr to migrate and concentrate in the cathode chamber.
Late Quarternary Sedimentation in the Eastern Angola Basin.
1973-11-01
Angola diapir field. Illite and montmorillonite are abundant in the southern part of the basin, reflecting the source in soils of South West Africa and...northward transport in the Benguela Current system. Kaolinite dominates the clay-mineral assemblage in the north-central part of the basin
The perspectives, information and conclusions conveyed in research project abstracts, progress reports, final reports, journal abstracts and journal publications convey the viewpoints of the principal investigator and may not represent the views and policies of ORD and EPA. Concl...
USDA-ARS?s Scientific Manuscript database
Columnaris disease, caused by the bacterial pathogen Flavobacterium columnare, continues to be a major problem worldwide in aquaculture settings. Despite the far-reaching negative impacts of columnaris disease, safe and efficacious preventatives and curatives for this disease remain limited. In th...
Irreversibility of 2,4-Dichlorophenoxyacetic Acid Sorption onto a Volcanic Ash Soil
NASA Astrophysics Data System (ADS)
Mon, E.; Kawamoto, K.; Komatsu, T.; Moldrup, P.
2008-12-01
Pesticide sorption and desorption in soils are key processes governing fate and transport of pesticides in the soil environment. The irreversibility (or hysteresis) in the processes of pesticide sorption and desorption needs to be known to accurately predict behavior of pesticides in soil systems. 2,4-dichlorophenoxyacetic acid (2,4-D) is a widely used pesticide in agriculture fields. However, only few studies of 2,4-D adsorption onto Andosols (volcanic ash soils) have been published, and the knowledge of 2,4-D desorption onto Andosols is very limited. In this study, a volcanic ash soil sampled from a pasture site in Nishi-Tokyo, Japan was used as a sorbent in order to investigate the irreversibility of 2,4-D sorption. For comparison, a pure clay mineral (kaolinite) obtained from Clay Science Society of Japan (CSSJ) was also used. 2,4-D solutions with three concentrations (0.011, 0.022 and 0.045 mmol/L) were prepared in artificial rain water (ARW= 0.085mM NaCl + 0.015mM CaCl2) to simulate field conditions. To prepare the sample solutions, the solid mass/liquid volume ratio of 1:10 was used for both sorbents (volcanic ash soil and kaolinite). The experiments were conducted in triplicate using a batch method under different pH conditions to examine the effect of pH. Desorption was measured during a equilibration procedure: After removal of 7 mL of supernatant in the sorption step, 7 mL of ARW excluding 2,4-D was added to the sample solution after which, it was equilibrated and centrifuged. The procedure was performed sequentially three or four times to obtain a desorption isotherm. Sorption and desorption generally followed Freundlich isotherms. The results showed markedly effects of pH on 2,4-D sorption and desorption in both the soil and kaolinite, with the percentage of sorption increasing with decreasing pH whereas the percentage of desorption decreased. There was a larger adsorption-desorption hysteresis in the volcanic ash soil as compared to kaolinite. Moreover, the largest hysteresis was found under the lowest pH condition indicating that the hysteretic effect likely depended on the variation of pH. In summary, the volcanic ash soil exhibited higher sorption coefficients and hysteresis than kaolinite, likely due to soil properties such as high organic matter content and the presence of different clay minerals.
Toxicological evaluation of clay minerals and derived nanocomposites: a review.
Maisanaba, Sara; Pichardo, Silvia; Puerto, María; Gutiérrez-Praena, Daniel; Cameán, Ana M; Jos, Angeles
2015-04-01
Clays and clay minerals are widely used in many facets of our society. This review addresses the main clays of each phyllosilicate groups, namely, kaolinite, montmorillonite (Mt) and sepiolite, placing special emphasis on Mt and kaolinite, which are the clays that are more frequently used in food packaging, one of the applications that are currently exhibiting higher development. The improvements in the composite materials obtained from clays and polymeric matrices are remarkable and well known, but the potential toxicological effects of unmodified or modified clay minerals and derived nanocomposites are currently being investigated with increased interest. In this sense, this work focused on a review of the published reports related to the analysis of the toxicological profile of commercial and novel modified clays and derived nanocomposites. An exhaustive review of the main in vitro and in vivo toxicological studies, antimicrobial activity assessments, and the human and environmental impacts of clays and derived nanocomposites was performed. From the analysis of the scientific literature different conclusions can be derived. Thus, in vitro studies suggest that clays in general induce cytotoxicity (with dependence on the clay, concentration, experimental system, etc.) with different underlying mechanisms such as necrosis/apoptosis, oxidative stress or genotoxicity. However, most of in vivo experiments performed in rodents showed no clear evidences of systemic toxicity even at doses of 5000mg/kg. Regarding to humans, pulmonary exposure is the most frequent, and although clays are usually mixed with other minerals, they have been reported to induce pneumoconiosis per se. Oral exposure is also common both intentionally and unintentionally. Although they do not show a high toxicity through this pathway, toxic effects could be induced due to the increased or reduced exposure to mineral elements. Finally, there are few studies about the effects of clay minerals on wildlife, with laboratory trials showing contradictory outcomes. Clay minerals have different applications in the environment, thus with a strict control of the concentrations used, they can provide beneficial uses. Despite the extensive number of reports available, there is also a need of systematic in vitro-in vivo extrapolation studies, with still scarce information on toxicity biomarkers such as inmunomodulatory effects or alteration of the genetic expression. In conclusion, a case by case toxicological evaluation is required taking into account that different clays have their own toxicological profiles, their modification can change this profile, and the potential increase of the human/environmental exposure to clay minerals due to their novel applications. Copyright © 2014 Elsevier Inc. All rights reserved.
Heteroaggregation of Silver Nanoparticles with Clay Minerals in Aqueous System
NASA Astrophysics Data System (ADS)
Liu, J.; Burrow, E.; Hwang, Y.; Lenhart, J.
2013-12-01
Nanoparticles are increasingly being used in industrial processes and consumer products that exploit their beneficial properties and improve our daily lives. Nevertheless, they also attract attention when released into natural environment due to their potential for causing adverse effects. The fate and transport of nanoparticles in aqueous systems have been the focus of intense study. However, their interactions with other natural particles have received only limited attention. Clay minerals are ubiquitous in most aquatic systems and their variably charged surfaces can act as deposition sites that can alter the fate and transport of nanoparticles in natural aqueous environments. In this study, we investigated the homoaggregation of silver nanoparticles with different coating layers and their heteroaggregation behavior with clay minerals (illite, kaolinite, montmorillonite) in neutral pH solutions. Silver nanoparticles with a nominal diameter of 80 nm were synthesized with three different surface coating layers: uncoated, citrate-coated and Tween-coated. Illite (IMt-2), kaolinite (KGa-2), and montmorillonite (SWy-2) were purchased from the Clay Mineral Society (Indiana) and pretreated to obtain monocationic (Na-clay) and dicationic (Ca-clay) suspensions before the experiments. The change in hydrodynamic diameter as a function of time was monitored using dynamic light scattering (DLS) measurements in order to evaluate early stage aggregation as a function of electrolyte concentration in both the homo- and heteroaggregation scenarios. A shift in the critical coagulation concentration (CCC) values to lower electrolyte concentrations was observed in binary systems, compared to single silver nanoparticle and clay systems. The results also suggest more rapid aggregation in binary system during the early aggregation stage when compared to the single-particle systems. The behavior of citrate-coated silver nanoparticles was similar to that of the bare particles, while the Tween-coated silver nanoparticles showed high stability in both single and binary systems. There were no significant differences in early stage aggregation kinetics observed inthe Na-clay-nanoparticle or Ca-clay-nanoparticle systems, which suggested that the CCC values of the single Na- or Ca-clay suspensions depend only on the electrolyte concentration, not the original cations on the clay surface. These results provide a basic idea for understanding the heteroaggregation of different silver nanoparticles and clays, which can be utilized in further study of fate and transport of engineered nanoparticles in natural aqueous system.
Nonlinear Propagation of Sound in Recently Settled Flocculated Sediments
NASA Astrophysics Data System (ADS)
Reed, A. H.; Sanders, W. M.
2016-12-01
Cohesive sediments undergo changes in a whirlwind. Dumped out of the river and into the estuary, they get bathed in salty water and subject to turbulent motion. During this sequence of events, the clay particles form clay aggregates of larger size with higher settling rates than the clay particles. Once the flocs have settled, cohesive sediments may form a sediment deposit of mud. Our interest is in the factors that control the development of soundspeed within these muds. This paper addresses organic matter influences on floc aggregation and settling rates. In laboratory studies, organic matter type differed in mixtures with either bentonite or kaolinite clays. The organic matter types used were guar gum, a net positive biopolymer, and xanthan gum, a net negative biopolymer derived from bacterial exudates, similar to those commonly found in estuaries. These biopolymers were dissolved into low salinity water (0-10 ppt). The biopolymer mixture was degassed and during the degassing process, either bentonite or kaolinite clay was added to the vessel. Surprisingly, different settling rates occurred in the clay-biopolymer mixtures. The settling rates of the clay-guar mixtures was more rapid (1-2 days) than the settling rate for the clay-xanthan mixtures. While clay-guar consolidated further, clay-xanthan maintained consistency for more than 2 weeks with density slowly increasing during that period. Compressional soundspeed (Vp) measurements were made with depth through the vessel using 0.5 mHz piezoelectric transducers. It was found that Vp in water was similar to that of the clay-xanthan. Vp was the same in the upper 6 cm of mud as it was in the overlying water and Vp decreased to become slower with increasing depth. Compressional wave velocity (Vp) also changed slightly with the guar complexes below the sediment water interface to the depth of the vessel. Vp was slightly slower in the mud than in the water column. Vp of the water was 1480-1495 m/s whereas Vp within the clay-biopolymer was below the minimum Vp in the water column. This slight decrease in Vp with depth is consistent for that of naturally occurring surficial mud deposits. This work suggests that organic matter type can play a critical role in the rate of consolidation within a mud deposit, which has implications for mud strength development and transport potential.
Hatch, Courtney D; Gough, Raina V; Toon, Owen B; Tolbert, Margaret A
2008-01-17
Although critical to atmospheric modeling of stratospheric ozone depletion, selective heterogeneous nuclei that promote the formation of Type Ia polar stratospheric clouds (PSCs) are largely unknown. While mineral particles are known to be good ice nuclei, it is currently not clear whether they are also good nuclei for PSCs. In the present study, a high-vacuum chamber equipped with transmission Fourier transform infrared spectroscopy and a quadrupole mass spectrometer was used to study heterogeneous nucleation of nitric acid trihydrate (NAT) on two clay minerals-Na-montmorillonite and kaolinite-as analogs of atmospheric terrestrial and extraterrestrial minerals. The minerals are first coated with a 3:1 supercooled H2O/HNO3 solution prior to the observed nucleation of crystalline NAT. At 220 K, NAT formation was observed at low SNAT values of 12 and 7 on kaolinite and montmorillonite clays, respectively. These are the lowest SNAT values reported in the literature on any substrate. However, NAT nucleation exhibited significant temperature dependence. At lower temperatures, representative of typical polar stratospheric conditions, much higher supersaturations were required before nucleation was observed. Our results suggest that NAT nucleation on mineral particles, not previously treated with sulfuric acid, may not be an important nucleation platform for Type Ia PSCs under normal polar stratospheric conditions.
Maher, K.; Steefel, Carl; White, A.F.; Stonestrom, David A.
2009-01-01
In order to explore the reasons for the apparent discrepancy between laboratory and field weathering rates and to determine the extent to which weathering rates are controlled by the approach to thermodynamic equilibrium, secondary mineral precipitation, and flow rates, a multicomponent reactive transport model (CrunchFlow) was used to interpret soil profile development and mineral precipitation and dissolution rates at the 226 ka Marine Terrace Chronosequence near Santa Cruz, CA. Aqueous compositions, fluid chemistry, transport, and mineral abundances are well characterized [White A. F., Schulz M. S., Vivit D. V., Blum A., Stonestrom D. A. and Anderson S. P. (2008) Chemical weathering of a Marine Terrace Chronosequence, Santa Cruz, California. I: interpreting the long-term controls on chemical weathering based on spatial and temporal element and mineral distributions. Geochim. Cosmochim. Acta 72 (1), 36-68] and were used to constrain the reaction rates for the weathering and precipitating minerals in the reactive transport modeling. When primary mineral weathering rates are calculated with either of two experimentally determined rate constants, the nonlinear, parallel rate law formulation of Hellmann and Tisserand [Hellmann R. and Tisserand D. (2006) Dissolution kinetics as a function of the Gibbs free energy of reaction: An experimental study based on albite feldspar. Geochim. Cosmochim. Acta 70 (2), 364-383] or the aluminum inhibition model proposed by Oelkers et al. [Oelkers E. H., Schott J. and Devidal J. L. (1994) The effect of aluminum, pH, and chemical affinity on the rates of aluminosilicate dissolution reactions. Geochim. Cosmochim. Acta 58 (9), 2011-2024], modeling results are consistent with field-scale observations when independently constrained clay precipitation rates are accounted for. Experimental and field rates, therefore, can be reconciled at the Santa Cruz site. Additionally, observed maximum clay abundances in the argillic horizons occur at the depth and time where the reaction fronts of the primary minerals overlap. The modeling indicates that the argillic horizon at Santa Cruz can be explained almost entirely by weathering of primary minerals and in situ clay precipitation accompanied by undersaturation of kaolinite at the top of the profile. The rate constant for kaolinite precipitation was also determined based on model simulations of mineral abundances and dissolved Al, SiO2(aq) and pH in pore waters. Changes in the rate of kaolinite precipitation or the flow rate do not affect the gradient of the primary mineral weathering profiles, but instead control the rate of propagation of the primary mineral weathering fronts and thus total mass removed from the weathering profile. Our analysis suggests that secondary clay precipitation is as important as aqueous transport in governing the amount of dissolution that occurs within a profile because clay minerals exert a strong control over the reaction affinity of the dissolving primary minerals. The modeling also indicates that the weathering advance rate and the total mass of mineral dissolved is controlled by the thermodynamic saturation of the primary dissolving phases plagioclase and K-feldspar, as is evident from the difference in propagation rates of the reaction fronts for the two minerals despite their very similar kinetic rate laws. ?? 2009 Elsevier Ltd.
Mapping Acid Sulfate Alteration of Basaltic Andesite with Thermal Infrared Data
NASA Technical Reports Server (NTRS)
Vaughan, R. G.; Calvin, W. M.; Hook, S. J.; Taranik, J. V.
2002-01-01
Airborne thermal infrared multi- and hyperspectral data sets are used to map sulfate alteration of basaltic andesites near Reno, NV. Alteration includes quartz-alunite, jarosite and a number of clay minerals such as kaolinite and montmorillonite. Additional information is contained in the original extended abstract.
POLISHING INDUSTRIAL WASTE STREAM EFFLUENTS USING FLY ASH - NATURAL CLAY SORBENT COMBINATION
A laboratory evaluation of the use of acidic and basic fly ashes, bentonite, bauxite, illite, kaolinite, zeolite, vermiculite, and activated alumina is presented for polishing a 3.8 x 10 to the 6th power liters per day waste stream from the feldspar mining and processing industry...
NASA Astrophysics Data System (ADS)
Caniço, Ana; Duarte, Luís V.; Silva, Ricardo L.; Rocha, Fernando; Graciano Mendonça Filho, João
2015-04-01
The uppermost Sinemurian-Pliensbachian series of the western part of the Lusitanian Basin is composed by hemipelagic carbonates particularly enriched in organic matter. Great part of this succession, considered to be one of the most important potential source rock intervals of Portugal, crops out in the S. Pedro de Moel and Peniche sectors, belonging to the Água de Madeiros and Vale das Fontes formations. In this study, supported by a detailed and integrated stratigraphic framework, we analyzed 98 marly samples (whole-rock mineralogy and clay minerals assemblages) from the aforementioned formations in the S. Pedro de Moel and Peniche sectors. X-ray Diffraction analysis followed the standard procedures and the semi-quantification of the different mineral phases was calculated using MacDiff 4.2.6. The goals of this work are to demonstrate the vertical variability of the mineral composition of these two units and investigate the relationship between the clay minerals assemblages and the content in organic matter (Total organic carbon: TOC). Besides the abundance of calcite and phyllosilicates, whole-rock mineralogy revealed the presence of quartz, potassium feldspar, dolomite, and pyrite (trace amounts). Other minerals like anhydrite, barite and gypsum occur sporadically. The clay minerals assemblages are dominated by illite+illite/smectite mixed-layers (minimum of 59%), always associated with kaolinite (maximum of 37%) and chlorite (maximum of 25%); sporadically smectite occurs in trace amounts. Generally, high TOC levels (i.e., black shale facies with TOC reaching up to 22 wt.% in both units, see Duarte et al., 2010), show a major increase in chlorite and kaolinite (lower values of illite+illite/smectite mixed layers). A kaolinite enrichment is also observed just above the Sinemurian-Pliensbachian boundary (base of Praia da Pedra Lisa Member of Água de Madeiros Formation; values varying between 30 and 37%). This event is associated with a second-order regressive phase, and marks the disappearance of the organic-rich facies and increase of carbonate sedimentation. This enrichment was likely favored by the development of more humid conditions at the Sinemurian-Pliensbachian transition. References Duarte, L.V., Silva, R.L., Oliveira, L.C.V., Comas-Rengifo, M.J., Silva, F. 2010. Organic-rich facies in the Sinemurian and Pliensbachian of the Lusitanian Basin, Portugal: Total Organic Carbon distribution and relation to transgressive-regressive facies cycles. Geologica Acta 8, 325-340.
Sorption-desorption behavior of PCP on soil organic matter and clay minerals.
Pu, Xunchi; Cutright, Teresa J
2006-08-01
Pentachlorophenol (PCP) contamination is a severe environmental problem due to its widespread occurrence, toxicity and recalcitrance. In order to gain a better understanding of the fate of PCP in soils, the role of the soil organic matter (SOM) and clay minerals in the PCP sorption-desorption was studied on two bulk field soils, two subsoils (i.e., SOM or clay-removed soil) and two artificial soils. The two field soils used were a silty loam from New Mexico (NM) containing 10% clay and a sandy-clay-loam from Colombia (CO) South America comprised of 18% clay minerals. The bulk CO soil containing kaolinite sorbed significantly less PCP than the NM soil. All soils depicted an apparent hysteresis during sorption. The CO bulk and subsoils desorbed 14-20% and 15-26% of the sorbed PCP respectively whereas the NM bulk and subsoils desorbed only 4-12% and 5-16%, respectively. Experiments conducted with pure clay and artificial soils indicated that the expandable clay minerals were key sorbent material. Additional studies to investigate the interaction between SOM and clay minerals are needed to fully understand sorptive phenomena.
Toward Accurate Adsorption Energetics on Clay Surfaces
2016-01-01
Clay minerals are ubiquitous in nature, and the manner in which they interact with their surroundings has important industrial and environmental implications. Consequently, a molecular-level understanding of the adsorption of molecules on clay surfaces is crucial. In this regard computer simulations play an important role, yet the accuracy of widely used empirical force fields (FF) and density functional theory (DFT) exchange-correlation functionals is often unclear in adsorption systems dominated by weak interactions. Herein we present results from quantum Monte Carlo (QMC) for water and methanol adsorption on the prototypical clay kaolinite. To the best of our knowledge, this is the first time QMC has been used to investigate adsorption at a complex, natural surface such as a clay. As well as being valuable in their own right, the QMC benchmarks obtained provide reference data against which the performance of cheaper DFT methods can be tested. Indeed using various DFT exchange-correlation functionals yields a very broad range of adsorption energies, and it is unclear a priori which evaluation is better. QMC reveals that in the systems considered here it is essential to account for van der Waals (vdW) dispersion forces since this alters both the absolute and relative adsorption energies of water and methanol. We show, via FF simulations, that incorrect relative energies can lead to significant changes in the interfacial densities of water and methanol solutions at the kaolinite interface. Despite the clear improvements offered by the vdW-corrected and the vdW-inclusive functionals, absolute adsorption energies are often overestimated, suggesting that the treatment of vdW forces in DFT is not yet a solved problem. PMID:27917256
NASA Technical Reports Server (NTRS)
Coyne, L. M.; Costanzo, P. M.; Theng, B. K.
1989-01-01
Luminescence, induced by dehydration and by wetting with hydrazine and unsymmetrically substituted hydrazine, and related ESR spectra have been observed from several kaolinites, synthetically hydrated kaolinites, and metahalloysites. The amine-wetting luminescence results suggest that intercalation, not a chemiluminescence reaction, is the luminescence trigger. Correlation between hydration-induced luminescence and g = 2 ESR signals associated with O(-)-centres in several natural halloysites, and concurrent diminution of the intensity of both these signal types as a function of aging in two 8.4 angstroms synthetically hydrated, kaolinites, confirm a previously-reported relationship between the luminescence induced by dehydration and in the presence of O(-)-centres (holes, i.e., electron vacancies) in the tetrahedral sheet. Furthermore, the ESR spectra of the 8.4 angstroms hydrate showed a concurrent change in the line shape of the g = 4 signal from a shape usually associated with structural Fe in an ordered kaolinite, to a simpler one typically observed in more disordered kaolinite, halloysite, and montmorillonite. Either structural Fe centres and the O(-)-centres interact, or both are subject to factors previously associated with degree of order. The results question the long-term stability of the 8.4 angstroms hydrate, although XRD does not indicate interlayer collapse over this period. Complex inter-relationships are shown between intercalation, stored energy, structural Fe, and the degree of hydration which may be reflected in catalytic as well as spectroscopic properties of the clays.
A role for subducted super-hydrated kaolinite in Earth’s deep water cycle
DOE Office of Scientific and Technical Information (OSTI.GOV)
Hwang, Huijeong; Seoung, Donghoon; Lee, Yongjae
Water is the most abundant volatile component in the Earth. It continuously enters the mantle through subduction zones, where it reduces the melting temperature of rocks to generate magmas. The dehydration process in subduction zones, which determines whether water is released from the slab or transported into the deeper mantle, is an essential component of the deep water cycle. Here in this paper we use in situ and time-resolved high-pressure/high-temperature synchrotron X-ray diffraction and infrared spectra to characterize the structural and chemical changes of the clay mineral kaolinite. At conditions corresponding to a depth of about 75 km in amore » cold subducting slab (2.7 GPa and 200 °C), and in the presence of water, we observe the pressure-induced insertion of water into kaolinite. This super-hydrated phase has a unit cell volume that is about 31% larger, a density that is about 8.4% lower than the original kaolinite and, with 29 wt% H 2O, the highest water content of any known aluminosilicate mineral in the Earth. As pressure and temperature approach 19 GPa and about 800 °C, we observe the sequential breakdown of super-hydrated kaolinite. The formation and subsequent breakdown of super-hydrated kaolinite in cold slabs subducted below 200 km leads to the release of water that may affect seismicity and help fuel arc volcanism at the surface.« less
A role for subducted super-hydrated kaolinite in Earth’s deep water cycle
Hwang, Huijeong; Seoung, Donghoon; Lee, Yongjae; ...
2017-11-20
Water is the most abundant volatile component in the Earth. It continuously enters the mantle through subduction zones, where it reduces the melting temperature of rocks to generate magmas. The dehydration process in subduction zones, which determines whether water is released from the slab or transported into the deeper mantle, is an essential component of the deep water cycle. Here in this paper we use in situ and time-resolved high-pressure/high-temperature synchrotron X-ray diffraction and infrared spectra to characterize the structural and chemical changes of the clay mineral kaolinite. At conditions corresponding to a depth of about 75 km in amore » cold subducting slab (2.7 GPa and 200 °C), and in the presence of water, we observe the pressure-induced insertion of water into kaolinite. This super-hydrated phase has a unit cell volume that is about 31% larger, a density that is about 8.4% lower than the original kaolinite and, with 29 wt% H 2O, the highest water content of any known aluminosilicate mineral in the Earth. As pressure and temperature approach 19 GPa and about 800 °C, we observe the sequential breakdown of super-hydrated kaolinite. The formation and subsequent breakdown of super-hydrated kaolinite in cold slabs subducted below 200 km leads to the release of water that may affect seismicity and help fuel arc volcanism at the surface.« less
Kaolinite in pharmaceutics and biomedicine.
Awad, Mahmoud E; López-Galindo, Alberto; Setti, Massimo; El-Rahmany, Mahmoud M; Iborra, César Viseras
2017-11-25
Kaolinite Al 2 Si 2 O 5 (OH) 4 is an abundant and inexpensive geomaterial regarded as one of the most common clay minerals in the earth's crust and the most widespread phase among the other kaolin polymorphs (halloysite, dickite and nacrite). Structurally, it is a hydrous aluminum phyllosilicate member belonging to the dioctahedral 1:1 kaolin mineral group. The particle size of the pseudohexagonal kaolinite platelets is normally <2μm (if compared to a human red blood cell of a typical diameter 6.2-8.2μm or to a virus particle of about 50nm diameter). The kaolinite platelets, either stacked together with a common booklet-like shape in a highly ordered structure (well crystallized) or disordered structure (poorly crystallized), consist of layers considered as a strong dipole of hydrophobic siloxane surface dominated by negative charges, and the other hydrophilic aluminol surface carries positive charges. Kaolinite has been used in many pharmaceutical applications as excipient or active ingredient, because it exhibits excellent physical, chemical and surface physicochemical properties. In addition to their classical pharmaceutical uses, kaolinite and its derivatives have been recently considered as a promising material in many biomedical innovation areas such as drug, protein and gene delivery based on the high interaction capacities with organic and biochemical molecules, bioadhesion and cellular uptake. Pharmaceutical kaolin grades are considerably demanded for usage as excipient in formulations of solid and semi-solid dosage forms. The most important functionalities of kaolin used as excipient are reported as diluent, binder, disintegrant, pelletizing and granulating, amorphizing, particle film coating, emulsifying and suspending agent. Because of its uninjured bioactivity, kaolinite has been also used as active agent for treatment of some common diseases. It can be topically administered as hemostatic agent, dermatological protector, anti-inflammatory agent and in pelotherapy, or orally as gastrointestinal protector, and antibacterial, antiviral, detoxification or antidiarrheal agent. With these premises, the future of kaolinite in health-care uses is strongly interesting, especially in the development of pharmaceutical and cosmetic industries. In biomedicinal investigations, it can be considered as a promising natural geomaterial for designing new derivatives that can contribute in the trials of discovering new therapeutic systems and treatment pathways of global challenge diseases such as cancer, viruses, antibiotic resistant bacteria, alzheimer, chronic skeletomuscular and geriatric diseases. Copyright © 2017 Elsevier B.V. All rights reserved.
Evaluation of theoretical and empirical water vapor sorption isotherm models for soils
NASA Astrophysics Data System (ADS)
Arthur, Emmanuel; Tuller, Markus; Moldrup, Per; de Jonge, Lis W.
2016-01-01
The mathematical characterization of water vapor sorption isotherms of soils is crucial for modeling processes such as volatilization of pesticides and diffusive and convective water vapor transport. Although numerous physically based and empirical models were previously proposed to describe sorption isotherms of building materials, food, and other industrial products, knowledge about the applicability of these functions for soils is noticeably lacking. We present an evaluation of nine models for characterizing adsorption/desorption isotherms for a water activity range from 0.03 to 0.93 based on measured data of 207 soils with widely varying textures, organic carbon contents, and clay mineralogy. In addition, the potential applicability of the models for prediction of sorption isotherms from known clay content was investigated. While in general, all investigated models described measured adsorption and desorption isotherms reasonably well, distinct differences were observed between physical and empirical models and due to the different degrees of freedom of the model equations. There were also considerable differences in model performance for adsorption and desorption data. While regression analysis relating model parameters and clay content and subsequent model application for prediction of measured isotherms showed promise for the majority of investigated soils, for soils with distinct kaolinitic and smectitic clay mineralogy predicted isotherms did not closely match the measurements.
Pore space analysis of NAPL distribution in sand-clay media
Matmon, D.; Hayden, N.J.
2003-01-01
This paper introduces a conceptual model of clays and non-aqueous phase liquids (NAPLs) at the pore scale that has been developed from a mathematical unit cell model, and direct micromodel observation and measurement of clay-containing porous media. The mathematical model uses a unit cell concept with uniform spherical grains for simulating the sand in the sand-clay matrix (???10% clay). Micromodels made with glass slides and including different clay-containing porous media were used to investigate the two clays (kaolinite and montmorillonite) and NAPL distribution within the pore space. The results were used to understand the distribution of NAPL advancing into initially saturated sand and sand-clay media, and provided a detailed analysis of the pore-scale geometry, pore size distribution, NAPL entry pressures, and the effect of clay on this geometry. Interesting NAPL saturation profiles were observed as a result of the complexity of the pore space geometry with the different packing angles and the presence of clays. The unit cell approach has applications for enhancing the mechanistic understanding and conceptualization, both visually and mathematically, of pore-scale processes such as NAPL and clay distribution. ?? 2003 Elsevier Science Ltd. All rights reserved.
NASA Astrophysics Data System (ADS)
Beckerman, Laura Grace
The Mars Science Laboratory (MSL) Curiosity rover is equipped with CheMin, the first x-ray diffraction (XRD) instrument on Mars, for in situ mineralogy as part of its mission to seek evidence of past habitability at Gale Crater. Detection and characterization of hydrated minerals like clays and sulfates provides crucial insight into Mars' early geochemistry. For example, clays are often interpreted as having formed in lacustrine environments at neutral pHs, while sulfates such as jarosite are evidence of acid sulfate alteration. However, CheMin's inability to remove non-clay minerals and to preferentially orient samples may pose significant challenges to clay detection and characterization at Gale Crater. To evaluate the effect of particle size separation (<0.2 microm), removal of non-clay minerals, preferred orientation, and ethylene glycol solvation on XRD analyses of clays, we used both a CheMin analog instrument and a traditional laboratory XRD to identify clays in acid sulfate altered basalt from Mars analog sites in Costa Rica. We detected kaolinite in four of the fourteen samples studied, one of which also contained montmorillonite. Kaolinite was not detected in two samples with the analog instrument prior to clay isolation. These results suggest that CheMin may miss detection of some clays at Gale Crater, which could affect interpretations of early Mars' habitability. Mistaking iron-rich natroalunite (Na[Al,Fe]3(SO4) 2(OH)6) for jarosite (KFe3(SO4) 2(OH)6) could also impact interpretations of early Mars, as natroalunite can form over a broader range of pH, water:rock ratios, and redox conditions than can jarosite. To determine if iron-rich natroalunite is a common alteration product at Mars analog sites, we assessed iron content in natroalunite from Costa Rica. We detected up to 30% iron substitution in natroalunite at diverse geochemical settings. We also evaluated the feasibility of using XRD or Raman spectroscopy for in situ iron-rich natroalunite detection, and determined that CheMin on Curiosity and the Raman Laser Spectrometer on the upcoming ExoMars rover could detect natroalunite with ≥25% iron substitution. Distinguishing between iron-rich natroalunite and jarosite with CheMin could aid in interpreting geochemical conditions and habitability at Gale Crater.
A laboratory study of colloid and solute transport in surface runoff on saturated soil
NASA Astrophysics Data System (ADS)
Yu, Congrong; Gao, Bin; Muñoz-Carpena, Rafael; Tian, Yuan; Wu, Lei; Perez-Ovilla, Oscar
2011-05-01
SummaryColloids in surface runoff may pose risks to the ecosystems not only because some of them (e.g., pathogens) are toxic, but also because they may facilitate the transport of other contaminants. Although many studies have been conducted to explore colloid fate and transport in the environment, current understanding of colloids in surface runoff is still limited. In this study, we conducted a range of laboratory experiments to examine the transport behavior of colloids in a surface runoff system, made of a soil box packed with quartz sand with four soil drainage outlets and one surface flow outlet. A natural clay colloid (kaolinite) and a conservative chemical tracer (bromide) were applied to the system under a simulated rainfall event (64 mm/h). Effluent soil drainage and surface flow samples were collected to determine the breakthrough concentrations of bromide and kaolinite. Under the experimental conditions tested, our results showed that surface runoff dominated the transport processes. As a result, kaolinite and bromide were found more in surface flow than in soil drainage. Comparisons between the breakthrough concentrations of bromide and kaolinite showed that kaolinite had lower mobility than bromide in the subsurface flow (i.e., soil drainage), but behaved almost identical to bromide in the surface runoff. Student's t-test confirmed the difference between kaolinite and bromide in subsurface flow ( p = 0.02). Spearman's test and linear regression analysis, however, showed a strong 1:1 correlation between kaolinite and bromide in surface runoff ( p < 0.0001). Our result indicate that colloids and chemical solutes may behave similarly in overland flow on bare soils with limited drainage when surface runoff dominates the transport processes.
Surface complexation model of uranyl sorption on Georgia kaolinite
Payne, T.E.; Davis, J.A.; Lumpkin, G.R.; Chisari, R.; Waite, T.D.
2004-01-01
The adsorption of uranyl on standard Georgia kaolinites (KGa-1 and KGa-1B) was studied as a function of pH (3-10), total U (1 and 10 ??mol/l), and mass loading of clay (4 and 40 g/l). The uptake of uranyl in air-equilibrated systems increased with pH and reached a maximum in the near-neutral pH range. At higher pH values, the sorption decreased due to the presence of aqueous uranyl carbonate complexes. One kaolinite sample was examined after the uranyl uptake experiments by transmission electron microscopy (TEM), using energy dispersive X-ray spectroscopy (EDS) to determine the U content. It was found that uranium was preferentially adsorbed by Ti-rich impurity phases (predominantly anatase), which are present in the kaolinite samples. Uranyl sorption on the Georgia kaolinites was simulated with U sorption reactions on both titanol and aluminol sites, using a simple non-electrostatic surface complexation model (SCM). The relative amounts of U-binding >TiOH and >AlOH sites were estimated from the TEM/EDS results. A ternary uranyl carbonate complex on the titanol site improved the fit to the experimental data in the higher pH range. The final model contained only three optimised log K values, and was able to simulate adsorption data across a wide range of experimental conditions. The >TiOH (anatase) sites appear to play an important role in retaining U at low uranyl concentrations. As kaolinite often contains trace TiO2, its presence may need to be taken into account when modelling the results of sorption experiments with radionuclides or trace metals on kaolinite. ?? 2004 Elsevier B.V. All rights reserved.
δ30Si systematics in a granitic saprolite, Puerto Rico
Ziegler, Karen; Chadwick, Oliver A.; White, Arthur F.; Brzezinski, Mark A.
2005-01-01
Granite weathering and clay mineral formation impart distinct and interpretable stable Si isotope (δ30Si) signatures to their solid and aqueous products. Within a saprolite, clay minerals have δ30Si values ∼2.0‰ more negative than their parent mineral and the δ30Si signature of the bulk solid is determined by the ratio of primary to secondary minerals. Mineral-specific weathering reactions predominate at different depths, driving changes in differing δ30Sipore watervalues. At the bedrock-saprolite interface, dissolution of plagioclase and hornblende creates δ30Sipore water signatures more positive than granite by up to 1.2‰; these reactions are the main contributor of Si to stream water and determine its δ30Si value. Throughout the saprolite, biotite weathering releases Si to pore waters but kaolinite overgrowth formation modulates its contribution to pore-water Si. The influence of biotite on δ30Sipore water is greatest near the bedrock where biotite-derived Si mixes with bulk pore water prior to kaolinite formation. Higher in the saprolite, biotite grains have become more isolated by kaolinite overgrowth, which consumes biotite-derived Si that would otherwise influence δ30Sipore water. Because of this isolation, which shifts the dominant source of pore-water Si from biotite to quartz, δ30Sipore water values are more negative than granite by up to 1.3‰ near the top of the saprolite.
Tao, Kelin; Zhao, Song; Gao, Pin; Wang, Lijin; Jia, Hanzhong
2018-06-06
Interactions between microorganisms and minerals have the potential contribution to remove polycyclic aromatic hydrocarbons (PAHs) in model systems. In this study, phenanthrene (PHE) was used as a probe molecule to explore the potential adsorption and biotransformation processes in the presence of microorganisms and various reference clays, such as montmorillonite (M), kaolinite (K), and pyrophyllite (P). Equilibrium adsorption experiments and scanning electron microscopy (SEM) technique were used to investigate the sorption of Pantoea agglomerans strains on clay minerals saturated with cations (Na + and Fe 3+ ). The adsorption isotherms of PHE and Pantoea agglomerans strains on cation-modified clay minerals fitted to Langmuir equation, and their adsorbed amounts both followed the sequence: montmorillonite > kaolinite > pyrophyllite. For six types of cation-modified minerals, the behavior of PHE adsorbed and Pantoea agglomerans adhered onto mentioned minerals was in the order of Na(I)-M > Fe(Ⅲ)-M, Na(I)-K > Fe(Ⅲ)-K and Fe(Ⅲ)-P > Na(I)-P, respectively. The biodegradation results showed that cation-modified clay minerals could enhance the biodegradation of PHE, ascribing to their large specific surface area, and cation exchange capability, as well as the difference in zeta potential between minerals and Pantoea agglomerans strains. Comparison of biodegradation rates displayed that PHE was degraded the highest in the presence of Na-M (93.285%). In addition, the obtained results suggested that the adhesion of bacteria onto cation-exchanged clay minerals was beneficial to the biodegradation of PHE. Anthracen-9-ylmethanol and 3,4-dimethyl-2-(3-methylbutanoyl)benzoic acid were detected as the main intermediate compounds, which can be further biodegraded into small molecules. The overall results obtained in this study are of valuable significance for the understanding of the behavior of PHE in soil and associated environment. Copyright © 2018 Elsevier Inc. All rights reserved.
NASA Astrophysics Data System (ADS)
Deng, Shaohui; Wang, Xiaoling; Yu, Jia; Zhang, Yichi; Liu, Zhen; Zhu, Yushan
2018-06-01
Grouting plays a crucial role in dam safety. Due to the concealment of grouting activities, complexity of fracture distribution in rock masses and rheological properties of cement grout, it is difficult to analyze the effects of grouting. In this paper, a computational fluid dynamics (CFD) simulation approach of dam foundation grouting based on a 3D fracture network model is proposed. In this approach, the 3D fracture network model, which is based on an improved bootstrap sampling method and established by VisualGeo software, can provide a reliable and accurate geometric model for CFD simulation of dam foundation grouting. Based on the model, a CFD simulation is performed, in which the Papanastasiou regularized model is used to express the grout rheological properties, and the volume of fluid technique is utilized to capture the grout fronts. Two sets of tests are performed to verify the effectiveness of the Papanastasiou regularized model. When applying the CFD simulation approach for dam foundation grouting, three technical issues can be solved: (1) collapsing potential of the fracture samples, (2) inconsistencies in the geometric model in actual fractures under complex geological conditions, and (3) inappropriate method of characterizing the rheological properties of cement grout. The applicability of the proposed approach is demonstrated by an illustrative case study—a hydropower station dam foundation in southwestern China.
Jelavić, S; Stipp, S L S; Bovet, N
2018-06-27
An understanding of the mechanisms that control the adsorption of organic molecules on clay minerals is of interest in several branches of science and industry. Oil production using low salinity injection fluids can increase yields by as much as 40% over standard injection with seawater or formation water. The mechanism responsible for the low salinity response is still debated, but one hypothesis is a change in pore surface wettability. Organic contamination in soil and drinking water aquifers is a challenge for municipal water suppliers and for agriculture. A better understanding is needed for how mineral species, solution composition and pH affect the desorption of low molecular weight organic ligands from clay minerals and consequently their wettability. We used X-ray photoelectron spectroscopy under cryogenic conditions to investigate the in situ composition in the mineral-solution interface region in a series of experiments with a range of pH and ion concentrations. We demonstrate that both chlorite and kaolinite release organic molecules under conditions relevant for low salinity water flooding. This release increases with a higher solution pH but is only slightly affected by the character of the organic ligand. This is consistent with the observation that low salinity enhanced oil recovery correlates with the presence of chlorite and kaolinite. Our results indicate that the pore surface charge and salinity of formation water and injection fluids are key parameters in determining the low salinity response. In general, our results imply that clay mineral surface charge influences the composition in the interface through an affinity for organic molecules.
NASA Technical Reports Server (NTRS)
Bishop, Janice L.; Drief, Ahmed; Dyar, Darby
2003-01-01
Clays, if present on Mars, have been illusive. Determining whether or not clay minerals and other aqueous alteration species are present on Mars provides key information about the extent and duration of aqueous processes on Mars. The purpose of this study is to characterize in detail changes in the mineral grains resulting from grinding and to assess the influence of physical processes on clay minerals on the surface of Mars. Physical alteration through grinding was shown to greatly affect the structure and a number of properties of antigorite and kaolinite. This project builds on an initial study and includes a combination of SEM, HRTEM, reflectance and M ssbauer spectroscopies. Grain size was found to decrease, as expected, with grinding. In addition, nanophase carbonate, Si-OH and iron oxide species were formed.
Using organic matter to increase soil fertility in Burundi: potentials and limitations
NASA Astrophysics Data System (ADS)
Kaboneka, Salvator
2015-04-01
Agriculture production in Burundi is dominated by small scale farmers (0.5 ha/household) who have only very limited access to mineral inputs. In the past, farmers have relied on fallow practices combined with farm yard manures to maintain and improve soil fertility. However, due to the high population growth and high population density (370/km²), fallow practices are nowadays no longer feasible, animal manures cannot be produced in sufficient quantities to maintain soil productivity and food insecurity has become a quasi permanent reality. Most Burundian soils are characterized by 1:1 types of clay minerals (kaolinite) and are acidic in nature. Such soils are of very low cation exchange capacity (CEC). To compare the effect of % clays and % organic matter (% C), correlations tests have been conducted between the two parameters and the CEC. It was found that in high altitude kaolinitic and acidic soils, CEC was highly correlated to % C and less correlated to % clay, suggesting that organic matter could play an important role in improving fertility and productivity of these soils. Based on these findings, additional studies have been conducted to evaluate the fertilizer and soil amendment values of animal manures (cattle, goat, chicken), and leguminous (Calliandra calothyrsus, Gliricidia sepium, Senna simea, Senna spectabilis) and non-leguminous (Tithonia diversifolia) foliar biomass. It was observed that chicken manure significantly reduces Al3+ levels in acidic soils, while Tithonia diversifolia outperforms in nutrient releases compared to the commonly known leguminous agroforestry shrubs and trees indicated above. Although the above mentioned organic sources can contribute to the soil nutrients supply, the quantities potentially available on farm are generally small. The only solution is to supplement these organic sources with other organic sources (compost, organic household waste), chemical fertilizers and mineral amendments (lime) to achieve Integrated Soil Fertility Management. The amendments with inorganic minerals must be on the one hand as specific as possible to function as a real site-specific fertilizer, on the other hand it should be a generic blend to make it less expensive. This is a dilemma, and requires new ways of balancing organic matter and nutrients in the soils. Key words: Kaolinitic and acidic soils, CEC, Organic matter, animal manures, foliar biomass.
Late Miocene to Pleistocene Mineralogy of ODP Site 1146
NASA Astrophysics Data System (ADS)
Arnold, E. M.
2001-12-01
ODP Site 1146 (19° 27.40'N, 116° 16.37'E, 2092 m depth) was drilled on the continental slope of the South China Sea. A composite section, comprised of three stratigraphic units, extends down to 640 mcd. Unit 1 is late Pliocene to Pleistocene nannofossil clay (0 - 243 mcd); Unit 2, middle Miocene to Late Pliocene foraminifera - nannofossil - clay mixed sediment (243 - 553 mcd); Unit 3, early to middle Miocene nannofossil clay (553 - 642 mcd). This study reports the < 2 μ m mineralogy from the late Miocene through early Pleistocene. Samples were analyzed at approximately 1.5 m intervals from 150 to 225 mcd, and 1 m intervals from 225 to 440 mcd, with an age resolution of ~25 ka and ~35 ka, respectively. Illite, chlorite, quartz and plagioclase concentrations decrease with increasing depth through Unit 1. Kaolinite and calcite concentrations increase with depth, while smectite values are constant in this unit. Illite, quartz and plagioclase show high variability in Unit 1 compared with the underlying Unit 2. Unit 2 has more uniform sediment composition, with constant illite, chlorite, and quartz concentrations. Kaolinite concentration increases with depth, following a drop in concentration across the Unit 1/2 boundary. Plagioclase concentration shows a small, steady decrease throughout this unit. Smectite concentration does not change across the Unit 1/2 boundary, decreases to a steady low value from 310 - 400 mcd, and increases again towards the bottom. The mineralogy of sediments recovered at Site 1146 suggest a classic pattern of source region aridification from the middle Pliocene through the Pleistocene, indicated in Unit 1 mineralogy as a decrease in kaolinite with decreasing depth, concomitant with an increase in quartz, plagioclase, illite and chlorite. The mineral variability in this interval suggests glacial - interglacial control of the terrigenous sedimentation. The sediment sources and source area weathering regimes were relatively constant throughout Unit 2, as indicated by low mineral variability and relatively constant mineral concentrations.
NASA Astrophysics Data System (ADS)
Fox, A.; Packman, A. I.; Preziosi-Ribero, A.; Li, A.; Arnon, S.
2017-12-01
Sediment transport and deposition in streams can affect streambed hydraulic characteristics due to clogging, reduce water fluxes through the hyporheic zone, and thus expected to affect biogeochemical processes. Processes affecting deposition of suspended particles were systematically studied under various overlying velocities but without taking into account the interactions with groundwater. This is despite the fact that the interaction with groundwater were shown to play an important role in deposition patterns of fine sediments in field studies. The objective of this study was to evaluate the effect of losing and gaining fluxes on suspended sediment depositional patterns and on hyporheic exchange fluxes. Experiments were conducted in a laboratory flume system (640 cm long and 30 cm wide) that has a capacity to enforce losing or gaining flow conditions. The flume was packed with homogenous sand, while suspended sediment deposition was evaluated by adding kaolinite particles to the water and following the deposition rate by particle disappearance from the bulk water. Consecutive additions of kaolinite were done, while hyporheic exchange fluxes were evaluated by conducting NaCl tracer experiments between each kaolinite additions. Furthermore, dye injections were used to visualize the flow patterns in the streambed using time-lapse photography through the transparent sidewalls of the flume. Hyporheic exchange and particle tracking simulations were done to assess the results of particle deposition and feedbacks between hyporheic flow, particle transport, and streambed clogging. Experimental results showed that the deposition of clay decreases with increasing amount of clay concentration in the sediment. Hyporheic exchange flux decreases linearly with increasing amount of clay added to the system and the region of active hyporheic exchange was confined to the upper part of the sediment. Understanding the particle deposition mechanisms under losing and gaining flow condition are expected to improve our predictive ability to capture the dynamics of streambed characteristics, which has implications to sediment transport, biogeochemical processes and hyporheic ecology.
NASA Astrophysics Data System (ADS)
Kumar, Naveen; Zhao, Cunlu; Klaassen, Aram; van den Ende, Dirk; Mugele, Frieder; Siretanu, Igor
2016-02-01
Most solid surfaces, in particular clay minerals and rock surfaces, acquire a surface charge upon exposure to an aqueous environment due to adsorption and/or desorption of ionic species. Macroscopic techniques such as titration and electrokinetic measurements are commonly used to determine the surface charge and ζ -potential of these surfaces. However, because of the macroscopic averaging character these techniques cannot do justice to the role of local heterogeneities on the surfaces. In this work, we use dynamic atomic force microscopy (AFM) to determine the distribution of surface charge on the two (gibbsite-like and silica-like) basal planes of kaolinite nanoparticles immersed in aqueous electrolyte with a lateral resolution of approximately 30 nm. The surface charge density is extracted from force-distance curves using DLVO theory in combination with surface complexation modeling. While the gibbsite-like and the silica-like facet display on average positive and negative surface charge values as expected, our measurements reveal lateral variations of more than a factor of two on seemingly atomically smooth terraces, even if high resolution AFM images clearly reveal the atomic lattice on the surface. These results suggest that simple surface complexation models of clays that attribute a unique surface chemistry and hence homogeneous surface charge densities to basal planes may miss important aspects of real clay surfaces.
Review: nanocomposites in food packaging.
Arora, Amit; Padua, G W
2010-01-01
The development of nanocomposites is a new strategy to improve physical properties of polymers, including mechanical strength, thermal stability, and gas barrier properties. The most promising nanoscale size fillers are montmorillonite and kaolinite clays. Graphite nanoplates are currently under study. In food packaging, a major emphasis is on the development of high barrier properties against the migration of oxygen, carbon dioxide, flavor compounds, and water vapor. Decreasing water vapor permeability is a critical issue in the development of biopolymers as sustainable packaging materials. The nanoscale plate morphology of clays and other fillers promotes the development of gas barrier properties. Several examples are cited. Challenges remain in increasing the compatibility between clays and polymers and reaching complete dispersion of nanoplates. Nanocomposites may advance the utilization of biopolymers in food packaging.
Ito, Akihiko; Wagai, Rota
2017-01-01
Clay-size minerals play important roles in terrestrial biogeochemistry and atmospheric physics, but their data have been only partially compiled at global scale. We present a global dataset of clay-size minerals in the topsoil and subsoil at different spatial resolutions. The data of soil clay and its mineralogical composition were gathered through a literature survey and aggregated by soil orders of the Soil Taxonomy for each of the ten groups: gibbsite, kaolinite, illite/mica, smectite, vermiculite, chlorite, iron oxide, quartz, non-crystalline, and others. Using a global soil map, a global dataset of soil clay-size mineral distribution was developed at resolutions of 2' to 2° grid cells. The data uncertainty associated with data variability and assumption was evaluated using a Monte Carlo method, and validity of the clay-size mineral distribution obtained in this study was examined by comparing with other datasets. The global soil clay data offer spatially explicit studies on terrestrial biogeochemical cycles, dust emission to the atmosphere, and other interdisciplinary earth sciences. PMID:28829435
Pan, Gang; Zhang, Ming-Ming; Chen, Hao; Zou, Hua; Yan, Hai
2006-05-01
Algal removal abilities of 26 clays/minerals were classified into three categories according to the 8-h equilibrium removal efficiency (Q8h) and removal rate at a clay loading of 0.7 g/L. Type I clays (sepiolite, talc, ferric oxide, and kaolinite) had a Q8h > 90%, a t50 (time needed to remove 50% of the algae) < 15 min, and a t80 < 2.5 h. Type II clays (6 clays) had a Q8h 50-90%, a t50 < 2.5 h, and a t80 > 2.5 h. Type III clays (14 clays) with Q8h < 50%, t50 > 8 h and t80 > 14 h had no practical value in removal of algal blooms. When the clay loading was reduced to 0.2 g/L, Q8h for all the 25 materials decreased to below 60%, except for sepiolite whose Q8h remained about 97%. The high efficiency for sepiolite to flocculate M. aeruginosa cells in freshwaters was due to the mechanism of netting and bridging effect.
Bio-grout based on microbially induced sand solidification by means of asparaginase activity
Li, Mengmeng; Fu, Qing-Long; Zhang, Qiuzhuo; Achal, Varenyam; Kawasaki, Satoru
2015-01-01
Bio-grout, a new ground improvement method, has been recently developed to improve the mechanical properties, decrease the permeability of porous materials, reinforce or repair cementitious materials and modify the properties of soil or sand. Bio-grout production depends on microbially induced calcite precipitation (MICP), which is driven mainly by an enzyme, urease. However, urease-based MICP process produces excessive ammonia, in addition to secondary pollution generated by urea that is used as substrate in it. In the present study, we reported asparaginase-based MICP process for sand bio-grout development using Bacillus megaterium, and results were also compared with urease-based bio-grouts. The asparaginase activity led to significantly less ammonia production compared to urease without compromising with desired properties of a novel grout. The UCS of bio-grout was obtained at 980 kPa, while the permeability was decreased substantially. The mineralogical composition of precipitated substance was identified as calcite using XRD and the crystal morphology was observed under SEM. The mass percentage of calcite in bio-grout was calculated by thermogravimetric analysis and XCT verified calcite precipitation in it. The results confirmed that biocalcification by means of bacterial asparaginase is a potential solution for geotechnical problems. The asparaginase-based MICP process could be of wider acceptance in future. PMID:26525435
Electromigration of Mn, Fe, Cu and Zn with citric acid in contaminated clay.
Pazos, M; Gouveia, S; Sanroman, M A; Cameselle, C
2008-07-01
Metal reactivity, speciation and solubility have an important influence in its transportation through a porous matrix by electrokinetics and, therefore, they dramatically affect the removal efficiency. This work deals with the effect of solubility and transport competition among several metals (Mn, Fe, Cu and Zn) during their transport through polluted clay. The unenhancement electrokinetic treatment results in a limited removal of the tested metals because they were retained into the kaolinite sample by the penetration of the alkaline front. Metals showed a removal degree in accordance with the solubility of the corresponding hydroxide and its formation pH. In 7 days of treatment, the removal results were: 75.6% of Mn; 68.5% of Zn, 40.6% of Cu and 14.8% of Fe. In order to avoid the negative effects of the basic front generated at the cathode, two different techniques were proposed and tested: the addition of citric acid as complexing agent to the polluted kaolinite sample and the use of citric acid to control de pH on the cathode chamber. Both techniques are based on the capability of citric acid to act as a complexing and neutralizing agent. Almost complete removal of Mn, Cu and Zn was achieved when citric acid was used (as neutralizing or complexing agent). But Fe only reached 33% of removal because it formed a negatively charged complex with citrate that retarded its transportation to the cathode.
Using IKONOS Imagery to Estimate Surface Soil Property Variability in Two Alabama Physiographies
NASA Technical Reports Server (NTRS)
Sullivan, Dana; Shaw, Joey; Rickman, Doug
2005-01-01
Knowledge of surface soil properties is used to assess past erosion and predict erodibility, determine nutrient requirements, and assess surface texture for soil survey applications. This study was designed to evaluate high resolution IKONOS multispectral data as a soil- mapping tool. Imagery was acquired over conventionally tilled fields in the Coastal Plain and Tennessee Valley physiographic regions of Alabama. Acquisitions were designed to assess the impact of surface crusting, roughness and tillage on our ability to depict soil property variability. Soils consisted mostly of fine-loamy, kaolinitic, thermic Plinthic Kandiudults at the Coastal Plain site and fine, kaolinitic, thermic Rhodic Paleudults at the Tennessee Valley site. Soils were sampled in 0.20 ha grids to a depth of 15 cm and analyzed for % sand (0.05 - 2 mm), silt (0.002 -0.05 mm), clay (less than 0.002 mm), citrate dithionite extractable iron (Fe(sub d)) and soil organic carbon (SOC). Four methods of evaluating variability in soil attributes were evaluated: 1) kriging of soil attributes, 2) co-kriging with soil attributes and reflectance data, 3) multivariate regression based on the relationship between reflectance and soil properties, and 4) fuzzy c-means clustering of reflectance data. Results indicate that co-kriging with remotely sensed data improved field scale estimates of surface SOC and clay content compared to kriging and regression methods. Fuzzy c-means worked best using RS data acquired over freshly tilled fields, reducing soil property variability within soil zones compared to field scale soil property variability.
González-Costa, Juan José; Reigosa, Manuel Joaquín; Matías, José María; Fernández-Covelo, Emma
2017-01-01
This study determines the influence of the different soil components and of the cation-exchange capacity on the adsorption and retention of different heavy metals: cadmium, chromium, copper, nickel, lead and zinc. In order to do so, regression models were created through decision trees and the importance of soil components was assessed. Used variables were: humified organic matter, specific cation-exchange capacity, percentages of sand and silt, proportions of Mn, Fe and Al oxides and hematite, and the proportion of quartz, plagioclase and mica, and the proportions of the different clays: kaolinite, vermiculite, gibbsite and chlorite. The most important components in the obtained models were vermiculite and gibbsite, especially for the adsorption of cadmium and zinc, while clays were less relevant. Oxides are less important than clays, especially for the adsorption of chromium and lead and the retention of chromium, copper and lead. PMID:28072849
NASA Astrophysics Data System (ADS)
Cai, G.
2013-12-01
*Guanqiang Cai caiguanqiang@sina.com Guangzhou Marine Geological Survey, Guangzhou, 510760, P.R. China As the largest marginal sea in the western pacific, the South China Sea (SCS) receives large amount of terrigenous material annually through numerous rivers from surrounding continents and islands, which make it as the good place for the study of source to sink process. Yet few studies put emphasis on the northwestern continental shelf and slope in the SCS, even though most of the detrital materials derived from the Red River and Hainan Island are deposited in this area, and northwestern shelf plays a significant role in directly linking the South China, the Indochina and the South China Sea and thus controlling the source to sink process of terrestrial sediment. We presented the clay mineral and Sr-Nd isotopic composition of fine-grained fraction for sediments from northwestern SCS, in order to identify sediment source and transportation. The results show that the clay mineral of northwestern SCS sediments are mainly illite (30%~59%), smectite (20%~40%) and kaolinite (8%~35%), with minor chlorite. The illite chemical index varies between 0.19 and 0.75 with an average of 0.49, indicating an intensive hydrolysis in the source region. The 87Sr/86Sr ratios of sediments range from 0.716288 to 0.734416 (average of 0.724659), and ɛ Nd(0) values range from -10.31 to -11.62 (average of -10.93), which suggest that the source rocks of these sediments are derived from continental crust. The Hainan Island is an important source for sediments deposited in the nearshore and western shelf, especially for illite, kaolinite and smectite clay minerals. Furthermore, the relatively high contents of kaolinite and smectite in sediments from eastern shelf and southern slope of Hainan Island are also controlled by the supply of terrigenous materials from Hainan, which cannot be resulted from sedimentary differentiation of the Pearl and Red river sediments. And the correlation analysis between smectite and Sr-Nd isotopic ratios imply that the smectite in sediments mainly come from chemical weathering products of old continental crust, rather than volcanic rocks of Luzon island.
Keller, Margaret A.; Macquaker, Joe H.S.; Taylor, Kevin G.; Polya, David
2014-01-01
Diagenesis significantly impacts mudstone lithofacies. Processes operating to control diagenetic pathways in mudstones are poorly known compared to analogous processes occurring in other sedimentary rocks. Selected organic-carbon-rich mudstones, from the Kimmeridge Clay and Monterey Formations, have been investigated to determine how varying starting compositions influence diagenesis.The sampled Kimmeridge Clay Formation mudstones are organized into thin homogenous beds, composed mainly of siliciclastic detritus, with some constituents derived from water-column production (e.g., coccoliths, S-depleted type-II kerogen, as much as 52.6% total organic carbon [TOC]) and others from diagenesis (e.g., pyrite, carbonate, and kaolinite). The sampled Monterey Formation mudstones are organized into thin beds that exhibit pelleted wavy lamination, and are predominantly composed of production-derived components including diatoms, coccoliths, and foraminifera, in addition to type-IIS kerogen (as much as 16.5% TOC), and apatite and silica cements.During early burial of the studied Kimmeridge Clay Formation mudstones, the availability of detrital Fe(III) and reactive clay minerals caused carbonate- and silicate-buffering reactions to operate effectively and the pore waters to be Fe(II) rich. These conditions led to pyrite, iron-poor carbonates, and kaolinite cements precipitating, preserved organic carbon being S-depleted, and sweet hydrocarbons being generated. In contrast, during the diagenesis of the sampled Monterey Formation mudstones, sulfide oxidation, coupled with opal dissolution and the reduced availability of both Fe(III) and reactive siliciclastic detritus, meant that the pore waters were poorly buffered and locally acidic. These conditions resulted in local carbonate dissolution, apatite and silica cements precipitation, natural kerogen sulfurization, and sour hydrocarbons generation.Differences in mud composition at deposition significantly influence subsequent diagenesis. These differences impact their source rock attributes and mechanical properties.
Effect of Mineral and Microbe Interactions on Biomass Yield
NASA Astrophysics Data System (ADS)
Pena, S. A.; Block, K. A.; Katz, A.; Gottlieb, P.
2016-12-01
The ecological feedback of microbes (bacteria and viruses) in association with minerals is virtually unexplored in the context of characterizing how carbon cycles in the terrestrial ecosystem. These interactions include the ability for bacteriophage to control bacteria populations, the ability of minerals to provide a substrate for bacteria growth, and the effect of minerals on bacteriophage viability. We investigate bacteriophage aggregation with minerals in the clay size fraction (< 0.2 µm) as well as the interaction between bacteriophage and mineral biofilms. In our virus experiments, bacteriophage Φ6 was suspended with the minerals smectite, illite, kaolinite, and goethite at low divalent cation concentrations so aggregation was in the reaction limited colloidal aggregation (RLCA) regime, at neutral pH and room temperature conditions. Virus remained viable at a 1:1 virus-clay ratio for clays, and at an approximate 100:1 ratio for goethite. However, the number of plaque forming units was reduced by 99%. Electron micrographs show viable as well as partially disassembled virus, similar to the results found by Block et al. 2014. We found that inactivation of a 4 x 1011 cm-3 concentration of bacteriophage Φ6 by smectite, illite, kaolinite, and goethite, required a minimum sediment concentration of 1.5 x 1011 cm-3, 1.4 x 1011 cm-3, 2.5 x 1011 cm-3, and 1.1 x 109 cm-3, respectively. Mineral biofilms were generated by suspension of tropical soil clays with gram-positive and gram-negative microbes and characterized by x-ray diffraction and imaged by electron microscopy (SEM and TEM). Mineral biomass produced by gram negative organisms were subjected to virus infection to determine influence of minerals on community resilience. Lastly, we report biomass yield in each instance to quantify the influence of mineral composition on total biomass production.
Ruffell, Alastair; McKinley, Jennifer M; Worden, Richard H
2002-04-15
This paper reviews the opportunities and pitfalls associated with using clay mineralogical analysis in palaeoclimatic reconstructions. Following this, conjunctive methods of improving the reliability of clay mineralogical analysis are reviewed. The Mesozoic succession of NW Europe is employed as a case study. This demonstrates the relationship between clay mineralogy and palaeoclimate. Proxy analyses may be integrated with clay mineralogical analysis to provide an assessment of aridity-humidity contrasts in the hinterland climate. As an example, the abundance of kaolinite through the Mesozoic shows that, while interpretations may be difficult, the Mesozoic climate of NW Europe was subject to great changes in rates of continental precipitation. We may compare sedimentological (facies, mineralogy, geochemistry) indicators of palaeoprecipitation with palaeotemperature estimates. The integration of clay mineralogical analyses with other sedimentological proxy indicators of palaeoclimate allows differentiation of palaeoclimatic effects from those of sea-level and tectonic change. We may also observe how widespread palaeoclimate changes were; whether they were diachronous or synchronous; how climate, sea level and tectonics interact to control sedimentary facies and what palaeoclimate indicators are reliable.
Photodegradation of decabromodiphenyl ether adsorbed onto clay minerals, metal oxides, and sediment.
Ahn, Mi-Youn; Filley, Timothy R; Jafvert, Chad T; Nies, Loring; Hua, Inez; Bezares-Cruz, Juan
2006-01-01
The photodebromination of decabromodiphenyl ether (BDE-209) adsorbed onto six different solid matrixes was investigated in sunlight and by irradiation with 350 +/- 50 nm lamps (four lamps at 24 W each). After 14 days of lamp irradiation, BDE-209 degraded with a half-life of 36 and 44 days, respectively, on montmorillonite or kaolinite, with much slower degradation occurring when sorbed on organic carbon-rich natural sediment (t1/2 = 150 days). In late summer and fall sunlight (40.5 degrees N, elevation 600 ft), the half-lives of BDE-209 sorbed on montmorillonite and kaolinite were 261 and 408 days, respectively. Under both irradiation schemes, no significant loss of BDE-209 occurred when sorbed to aluminum hydroxide, iron oxide (ferrihydrite), or manganese dioxide (birnessite). Upon exposure to both lamp and solar light and in the presence of montmorillonite and kaolinite, numerous lesser brominated congeners (tri- to nonabromodiphenyl ethers) were produced. Nearly identical product distribution was evident on montmorillonite and kaolinite. Dark control experiments for each mineral showed no disappearance of BDE-209 or appearance of degradation products. These results suggest that photodegradation of BDE-209 on mineral aerosols during long-range atmospheric transport may be an important fate process for BDE-209 in the environment.
NASA Astrophysics Data System (ADS)
Kuwahara, Yoshihiro; Masudome, Yukiko; Paudel, Mukunda Raj; Fujii, Rie; Hayashi, Tatsuya; Mampuku, Mami; Sakai, Harutaka
2010-03-01
This paper reports the results of clay mineral analysis (the amount of clay fraction, clay mineral assemblages, illite crystallinity) of samples collected from a drilled core (Rabibhawan (RB) core) located in the west-central part of the Kathmandu Basin on the southern slope of the Central Himalaya. The amount of clay fraction in the core sediments between 12 m and 45 m depth (corresponding to ca. 17-76 ka), which belong to the Kalimati Formation, is variable and shows three clay-poor zones (19-31 ka, 44-51 ka, and 66-75 ka). The variations correspond with those of illite crystallinity index (Lanson index (LI) and modified Lanson index (MLI)) and kaolinite/illite ratio as well as the fossil pollen and diatom records reported by previous workers. These data reveal the following transformations occurring during the weathering process in this area: micas(mainlymuscovite)→illite(→illite-smectitemixedlayermineral(R=1))→kaolinite The sedimentation rate (~ 50 cm/kyr) of clay-poor zones that correspond to dry climate intervals is only half that of clay-rich zones (~ 120 cm/kyr) that correspond to wet climate intervals, indicating weakened chemical weathering and erosion and low suspended discharge during dry climate intervals. The clay-poor zones commonly show unique laminite beds with very fine, authigenic calcite, which was probably precipitated under calm and high calcite concentration conditions caused by low precipitation and run-off. The variations between dry and wet conditions in this area as deduced from clay minerals appear to follow the Indian Summer Monsoon Index (ISMI) (30°N-30°S, 1 July) and northern hemisphere summer insolation (NHSI) signals (30°N) at 1 July, especially during the dry climate zones, whereas the wet maxima of the wet climate zones somewhat deviate from the strongest NHSI. On the other hand, the dry-wet records lead markedly the SPECMAP stack (by about 5000 years). These results suggest that the Indian summer monsoon precipitation was strongly controlled by the NHSI or summer insolation difference between the Himalayan-Tibetan Plateau and the subtropical Indian Ocean, showing a major fluctuation on the 23,000 years precessional cycle, and that it was not driven by changes in high-latitude ice volume, although the records of clay mineral indices during the wet intervals leave a question that other factors, in addition to insolation forcing, may play important roles in weathering, erosion, and sedimentation processes.
Infrared analysis of clay bricks incorporated with spent shea waste from the shea butter industry.
Adazabra, A N; Viruthagiri, G; Shanmugam, N
2017-04-15
The peculiar challenge of effective disposing abundant spent shea waste and the excellent compositional variation tolerance of clay material offered an impetus to examine the incorporation of spent shea waste into clay material as an eco-friendly disposal route in making clay bricks. For this purpose, the chemical constituent, mineralogical compositions and thermal behavior of both clay material and spent shea waste were initially characterized from which modelled brick specimens incorporating 5-20 wt% of the waste into the clay material were prepared. The clay material showed high proportions of SiO 2 (52.97 wt%) and Al 2 O 3 (27.10 wt%) indicating their rich kaolinitic content: whereas, the inert nature of spent shea waste was exhibited by their low oxide content. The striking similarities in infrared absorption bands of pristine clay material and clay materials incorporated with 15 wt% of spent shea waste showed that the waste incorporation had no impact on bond formation of the clay bricks. Potential performance benefits of developing bricks from clay material incorporated with spent shea waste included improved fluxing agents, economic sintering and making of sustainable bricks. Consequently, the analytical results authenticate the incorporation of spent shea waste into clay materials for various desired benefits aside being an environmental correct route of its disposal. Copyright © 2017 Elsevier Ltd. All rights reserved.
Code of Federal Regulations, 2014 CFR
2014-07-01
...) Solvent Kaolinite-type clay Solid diluent, carrier Lactic acid Solvent Lactic acid, 2-ethylhexyl ester (CAS Reg. No. 6283-86-9) Solvent Lactic acid, 2-ethylhexyl ester, (2S)- (CAS Reg. No. 186817-80-1) Solvent Lactic acid, n-propyl ester, (S); (CAS Reg. No. 53651-69-7) Solvent Lauryl alcohol Surfactant...
Bahmanyar, M A
2007-09-01
The effect of different rice cultivation periods on the properties of selected soils in alluvial plain were studied in Mazandaran province (north of Iran) in 2004. Soils were sampled form 0, 6, 16, 26 and over 40 years rice cultivation fields. In each treatment three soil profiles and six nearby auger holes were studied. The present study results indicated that continuous rice cultivation have changed soil moisture regime from xeric to aquic, soil color from brown to grayish, surface horizons from mollic to ochric epipedon and soil structure changed from granular or blocky to massive. Therefore, the soil order has changed from Mollisols to Inceptisols. No illuviation and eluviation of clay minerals occurred as a consequence of rice cultivation. X-ray diffraction analysis showed that clay minerals in non-rice cultivated field were illite, vermiculite, montmorillonite, kaolinite and chlorite, but in rice field were illite, montmorillonite, kaolinite and chlorite, respectively. In contrast of montmorillonite, the amount of illite and vermiculite have been decreased by increasing periods of rice cultivation. The pH values of the saturated soil surface in six weeks past plantation have shifted toward neutrality. While Eh value of non-paddy soils were about +90 mv, surface horizons of paddy soils at field conditions had Eh value about +40, -12, -84, -122 mv, respectively. The amounts of organic matter and available Fe, Mn, Zn and Cu were increased whereas available K was decreased in paddy soils.
Evaluation of the healing activity of therapeutic clay in rat skin wounds.
Dário, Giordana Maciel; da Silva, Geovana Gomes; Gonçalves, Davi Ludvig; Silveira, Paulo; Junior, Adilson Teixeira; Angioletto, Elidio; Bernardin, Adriano Michael
2014-10-01
The use of clays for therapeutic practice is widespread in almost all regions of the world. In this study the physicochemical and microbiological healing characteristics of a clay from Ocara, Brazil, popularly used for therapeutic uses, were analyzed. The presence of Ca, Mg, Al, Fe, and Si was observed, which initially indicated that the clay had potential for therapeutic use. The average particle size of the clay (26.3 μm) can induce the microcirculation of the skin and the XRD analysis shows that the clay is formed by kaolinite and illite, a swelling clay. During the microbiological evaluation there was the need to sterilize the clay for later incorporation into the pharmaceutical formula. The accelerated stability test at 50°C for 3 months has showed that the pharmaceutical formula remained stable with a shelf life of two years. After the stability test the wound-healing capacity of the formulation in rats was evaluated. It was observed that the treatment made with the formulation containing the Ocara clay showed the best results since the formula allowed greater formation of collagen fibers and consequent regeneration of the deep dermis after seven days of treatment and reepithelialization and continuous formation of granulation tissue at the 14th day. Copyright © 2014 Elsevier B.V. All rights reserved.
A Comparative Study of T1 and T2 Relaxation in Shale
NASA Astrophysics Data System (ADS)
Keating, K.; Obasi, C. C.; Pashin, J. C.
2015-12-01
Nuclear magnetic resonance (NMR) relaxation measurement have been used extensively in petroleum and, more recently, in groundwater resource evaluation to estimate the porosity, pore-size distributions, permeability, fluid saturation, and fluid mobility. In shale, the transverse decay rate of NMR signal is sensitive to the microporosity, but is also affected by the paramagnetic contributions of clay and other iron-bearing minerals. Furthermore, contrasts in the magnetic susceptibility of the mineral matrix and pore fluids that result in an inhomogeneous magnetic field within the pore space results in an extra term in transverse relaxation. These issues can cause errors in NMR-based estimates of pore-size distribution and permeability. In this study we compare T1 and T2 relaxation time distributions in order to study the molecular mechanism of relaxation in brine-saturated mixtures of clay and other common minerals. We collected measurements on a range of mixtures of clay minerals common in shale (illite, glauconite, celadonite, chamosite, montmorillonite and kaolinite) and pyrite. To constrain the interpretation of the NMR data, we measured the magnetic susceptibility and surface area of all samples. We are confident that by accounting for the presence and variations of clay and pyrite in shale, we can substantially improve both the NMR estimate of pore-size distribution and permeability.
Dinosaurs, spherules, and the “magic” layer: A new K-T boundary clay site in Wyoming
NASA Astrophysics Data System (ADS)
Bohor, Bruce F.; Triplehorn, Don M.; Nichols, Douglas J.; Millard, Hugh T., Jr.
1987-10-01
A new Cretaceous-Tertiary (K-T) boundary clay site has been found along Dogie Creek in Wyoming in the drainage of Lance Creek—the type area of the Lance Formation of latest Cretaceous age. The boundary clay was discovered in the uppermost part of the Lance Formation, 4 7 cm beneath the lowest lignite in the Paleocene Fort Union Formation and approximately 1 m above a fragmented dinosaur bone. The boundary clay consists of a basal kaolinitic claystone layer as much as 3 cm thick containing hollow goyazite spherules, overlain by a 2 3 mm smectitic layer (the “magic” layer) containing both shock-metamorphosed minerals and an iridium anomaly of 21 ppb. A palynological break coincides with the base of the claystone layer; numerous Late Cretaceous palynomorph species terminate at this boundary. The paleontological significance of this new boundary site lies in its close association with the well-studied assemblage of dinosaurs and other vertebrates and flora within the type area of the Lance Formation. The spherules at the Dogie Creek site are extremely well preserved by virtue of their replacement by the mineral goyazite. This preservation should facilitate the resolution of the origin of the spherules and of their host layer.
Color measurement of methylene blue dye/clay mixtures and its application using economical methods
NASA Astrophysics Data System (ADS)
Milosevic, Maja; Kaludjerovic, Lazar; Logar, Mihovil
2016-04-01
Identifying the clay mineral components of clay materials by staining tests is rapid and simple, but their applicability is restricted because of the mutual interference of the common components of clay materials and difficulties in color determination. The change of color with concentration of the dye is related to the use of colorants as a field test for identifying clay minerals and has been improved over the years to assure the accuracy of the tests (Faust G. T., 1940). The problem of measurement and standardization of color may be solved by combination of colors observed in staining tests with prepared charts of color chips available in the Munsell Book of Color, published by Munsell Color Co. Under a particular set of illumination conditions, a human eye can achieve an approximate match between the color of the dyed clay sample and that of a standard color chip, even though they do have different spectral reflectance characteristics. Experiments were carried out with diffuse reflectance spectroscopy on selected clay samples (three montmorillonite, three kaolinite and one mix-layer clay samples) saturated with different concentration of methylene blue dye solution. Dominant wavelength and purity of the color was obtained on oriented dry samples and calculated by use of the I. C. I. (x, y) - diagram in the region of 400-700 nm (reflectance spectra) without MB and after saturation with different concentrations of MB solutions. Samples were carefully photographed in the natural light environment and processed with user friendly and easily accessible applications (Adobe color CC and ColorHexa encyclopedia) available for android phones or tablets. Obtained colors were compared with Munsell standard color chips, RGB and Hexa color standards. Changes in the color of clay samples in their interaction with different concentration of the applied dye together with application of economical methods can still be used as a rapid fieldwork test. Different types of clay minerals can be distinguished by application of at least three concentrations of the methylene blue dye on the same sample and observing the color change in comparison with standardized color chips that can be easily obtained and free of charge. If the color tests are properly used in conjunction with other more complex analytical procedures, they can be helpful addition in identification of different clay minerals, especially montmorillonite and kaolinite minerals. - Faust G. T., 1940, Staining of clay minerals as a rapid means of identification in natural and beneficiated products, U. S. Bur. Mines, Investigation Report. N0.3522 - Munsell Color, Munsell Book of Color, 1942. Macbeth Division of Kollmorgen Corporation, Maryland, U.S.A. - https://color.adobe.com/create/color-wheel/ - http://www.colorhexa.com/
NASA Astrophysics Data System (ADS)
Dwi Yanti, Evi; Pratiwi, I.
2018-02-01
Clay's abundance has been widely used as industrial raw materials, especially ceramic and tile industries. Utilization of these minerals needs a thermal process for producing ceramic products. Two studies conducted by Septawander et al. and Chin C et al., showed the relationship between thermal behavior of clays and their chemical and mineralogical composition. Clays are characterized by XRD analysis and thermal analysis, ranging from 1100°C to 1200°C room temperature. Specimen of raw materials of clay which is used for the thermal treatment is taken from different geological conditions and formation. In raw material, Quartz is almost present in all samples. Halloysite, montmorillonite, and feldspar are present in Tanjung Morawa raw clay. KC and MC similar kaolinite and illite are present in the samples. The research illustrates the interrelationships of clay minerals and chemical composition with their heat behavior. As the temperature of combustion increases, the sample reduces a significant weight. The minerals which have undergone a transformation phase became mullite, cristobalite or illite and quartz. Under SEM analysis, the microstructures of the samples showed irregularity in shape; changes occurred due the increase of heat.
Syngouna, Vasiliki I; Chrysikopoulos, Constantinos V
2015-02-15
Suspended clay particles in groundwater can play a significant role as carriers of viruses, because, depending on the physicochemical conditions, clay particles may facilitate or hinder the mobility of viruses. This experimental study examines the effects of clay colloids on the transport of viruses in variably saturated porous media. All cotransport experiments were conducted in both saturated and partially saturated columns packed with glass beads, using bacteriophages MS2 and ΦX174 as model viruses, and kaolinite (KGa-1b) and montmorillonite (STx-1b) as model clay colloids. The various experimental collision efficiencies were determined using the classical colloid filtration theory. The experimental data indicated that the mass recovery of viruses and clay colloids decreased as the water saturation decreased. Temporal moments of the various breakthrough concentrations collected, suggested that the presence of clays significantly influenced virus transport and irreversible deposition onto glass beads. The mass recovery of both viruses, based on total effluent virus concentrations, was shown to reduce in the presence of suspended clay particles. Furthermore, the transport of suspended virus and clay-virus particles was retarded, compared to the conservative tracer. Under unsaturated conditions both clay particles facilitated the transport of ΦX174, while hindered the transport of MS2. Moreover, the surface properties of viruses, clays and glass beads were employed for the construction of classical DLVO and capillary potential energy profiles, and the results suggested that capillary forces play a significant role on colloid retention. It was estimated that the capillary potential energy of MS2 is lower than that of ΦX174, and the capillary potential energy of KGa-1b is lower than that of STx-1b, assuming that the protrusion distance through the water film is the same for each pair of particles. Moreover, the capillary potential energy is several orders of magnitude greater than the DLVO potential energy. Copyright © 2014 Elsevier Inc. All rights reserved.
Ceramic media amended with metal oxide for the capture of viruses in drinking water.
Brown, J; Sobsey, M D
2009-04-01
Ceramic materials that can adsorb and/or inactivate viruses in water may find widespread application in low-tech drinking-water treatment technologies in developing countries, where porous ceramic filters and ceramic granular media filters are increasingly promoted for that purpose. We examined the adsorption and subsequent inactivation of bacteriophages MS2 and (phiX-174 on five ceramic media in batch adsorption studies to determine media suitability for use in a ceramic water filter application. The media examined were a kaolinitic ceramic medium and four kaolinitic ceramic media amended with iron or aluminium oxides that had been incorporated into the kaolinitic clays before firing. Batch adsorption tests indicate increased sorption and inactivation of surrogate viruses by media amended with Fe and Al oxide, with FeOOH-amended ceramic inactivating all bacteriophages up to 8 log10. Unmodified ceramic was a poor adsorbent of bacteriophages at less than 1 log10 adsorption-inactivation and high recovery of sorbed phages. These studies suggest that contact with ceramic media, modified with electropositive Fe or Al oxides, can reduce bacteriophages in waters to a greater extent than unmodified ceramic.
Bioavailability of methyl parathion adsorbed on clay minerals and iron oxide.
Cai, Peng; He, Xiaomin; Xue, Aifang; Chen, Hao; Huang, Qiaoyun; Yu, Jun; Rong, Xinming; Liang, Wei
2011-01-30
Adsorption, desorption and degradation by Pseudomonas putida of methyl parathion (O,O-dimethyl O-p-nitrophenyl phosphorothioate) on montmorillonite, kaolinite and goethite were studied. Metabolic activities of methyl parathion-degrading bacteria P. putida in the presence of minerals were also monitored by microcalorimetry to determine the degradation mechanism of methyl parathion. Montmorillonite presented higher adsorption capacity and affinity for methyl parathion than kaolinite and goethite. The percentage of degradation of methyl parathion adsorbed on minerals by P. putida was in the order of montmorillonite>kaolinite>goethite. The presence of minerals inhibited the exponential growth and the metabolic activity of P. putida. Among the examined minerals, goethite exhibited the greatest inhibitory effect on bacterial activity, while montmorillonite was the least depressing. The biodegradation of adsorbed methyl parathion by P. putida is apparently not controlled by the adsorption affinity of methyl parathion on minerals and may be mainly governed by the activity of the methyl parathion-degrading bacteria. The information obtained in this study is of fundamental significance for the understanding of the behavior of methyl parathion in soil environments. Copyright © 2010 Elsevier B.V. All rights reserved.
Monitoring of Grouting Compactness in a Post-Tensioning Tendon Duct Using Piezoceramic Transducers
Jiang, Tianyong; Kong, Qingzhao; Wang, Wenxi; Huo, Linsheng; Song, Gangbing
2016-01-01
A post-tensioning tendon duct filled with grout can effectively prevent corrosion of the reinforcement, maintain bonding behavior between the reinforcement and concrete, and enhance the load bearing capacity of concrete structures. In practice, grouting of the post-tensioning tendon ducts always causes quality problems, which may reduce structural integrity and service life, and even cause accidents. However, monitoring of the grouting compactness is still a challenge due to the invisibility of the grout in the duct during the grouting process. This paper presents a stress wave-based active sensing approach using piezoceramic transducers to monitor the grouting compactness in real time. A segment of a commercial tendon duct was used as research object in this study. One lead zirconate titanate (PZT) piezoceramic transducer with marble protection, called a smart aggregate (SA), was bonded on the tendon and installed in the tendon duct. Two PZT patch sensors were mounted on the top outside surface of the duct, and one PZT patch sensor was bonded on the bottom outside surface of the tendon duct. In the active sensing approach, the SA was used as an actuator to generate a stress wave and the PZT sensors were utilized to detect the wave response. Cement or grout in the duct functions as a wave conduit, which can propagate the stress wave. If the cement or grout is not fully filled in the tendon duct, the top PZT sensors cannot receive much stress wave energy. The experimental procedures simulated four stages during the grout pouring process, which includes empty status, half grouting, 90% grouting, and full grouting of the duct. Experimental results show that the bottom PZT sensor can detect the signal when the grout level increases towards 50%, when a conduit between the SA and PZT sensor is formed. The top PZT sensors cannot receive any signal until the grout process is completely finished. The wavelet packet-based energy analysis was adopted in this research to compute the total signal energy received by PZT sensors. Experimental results show that the energy levels of the PZT sensors can reflect the degree of grouting compactness in the duct. The proposed method has the potential to be implemented to monitor the tendon duct grouting compactness of the reinforced concrete structures with post tensioning. PMID:27556470
Grout formulation for disposal of low-level and hazardous waste streams containing fluoride
McDaniel, E.W.; Sams, T.L.; Tallent, O.K.
1987-06-02
A composition and related process for disposal of hazardous waste streams containing fluoride in cement-based materials is disclosed. the presence of fluoride in cement-based materials is disclosed. The presence of fluoride in waste materials acts as a set retarder and as a result, prevents cement-based grouts from setting. This problem is overcome by the present invention wherein calcium hydroxide is incorporated into the dry-solid portion of the grout mix. The calcium hydroxide renders the fluoride insoluble, allowing the grout to set up and immobilize all hazardous constituents of concern. 4 tabs.
Aggregation of Montmorillonite and Organic Matter in Aqueous Media Containing Artificial Seawater
2009-01-23
laboratory kaolinite and montmorillonite aggregation in which the dispersion-aggregation properties of pure clay suspensions were found to be primarily...Article 3. DATES COVERED (From - To) 4. TITLE AND SUBTITLE Aggregation of montmorillonite and organic matter in aqueous media containing...properties of suspended colloids and aggregates) were determined for systems containing suspended montmorillonite , humic acid, and/or chitin at the
2011-03-25
implied is via iondipole forces.5,6 It is well-known that clays such as montmorillonite and kaolinite accelerate the degradation of insecticides such...REPORT Montmorillonite Functionalized with Pralidoxime As a Material for Chemical Protection against Organophosphorous Compounds 14. ABSTRACT 16...SECURITY CLASSIFICATION OF: Montmorillonite K-10 functionalized with ?-nucleophilic 2-pralidoxime (PAM) and its zwitterionic oximate form (PAMNa) is
Lithologic Control on Secondary Clay Mineral Formation in the Valles Caldera, New Mexico
NASA Astrophysics Data System (ADS)
Caylor, E.; Rasmussen, C.; Dhakal, P.
2015-12-01
Understanding the transformation of rock to soil is central to landscape evolution and ecosystem function. The objective of this study was to examine controls on secondary mineral formation in a forested catchment in the Catalina-Jemez CZO. We hypothesized landscape position controls the type of secondary minerals formed in that well-drained hillslopes favor Si-poor secondary phases such as kaolinite, whereas poorly drained portions of the landscape that collect solutes from surrounding areas favor formation of Si-rich secondary phases such as smectite. The study focused on a catchment in Valles Caldera in northern New Mexico where soils are derived from a mix of rhyolitic volcanic material, vegetation includes a mixed conifer forest, and climate is characterized by a mean annual precipitation of ~800 mm yr-1 and mean annual temperature of 4.5°C. Soils were collected at the soil-saprolite boundary from three landscape positions, classified as well drained hillslope, poorly drained convergent area, and poorly drained hill slope. Clay fractions were isolated and analyzed using a combination of quantitative and qualitative x-ray diffraction (XRD) analyses and thermal analysis. Quantitative XRD of random powder mounts indicated the presence of both primary phases such as quartz, and alkali and plagioclase feldspars, and secondary phases that include illite, Fe-oxyhydroxides including both goethite and hematite, kaolinite, and smectite. The clay fractions were dominated by smectite ranging from 36-42%, illite ranging from 21-35%, and kaolinite ranging from 1-8%. Qualitative XRD of oriented mounts confirmed the presence of smectite in all samples, with varying degrees of interlayering and interstratification. In contrast to our hypothesis, results indicated that secondary mineral assemblage was not strongly controlled by landscape position, but rather varied with underlying variation in lithology. The catchment is underlain by a combination of porphorytic rhyolite and hydrothermally altered rhyolitic tuff, with an intrusion of Paleozoic sandstone. Smectite content was generally greater in areas underlain by the tuff and likely represent a combination of both diagenic smectite formed by hydrothermal alteration of volcanic glass and authigenic smectites formed in the soils via chemical weathering.
REE concentration processes in ion adsorption deposits: Evidence from Madagascar and China.
NASA Astrophysics Data System (ADS)
Smith, Martin; Estrade, Guillaume; Marquis, Eva; Goodenough, Kathryn; Nasun, Peter; Cheng, Xu; Kynicky, Jindrich
2017-04-01
Lateritic clay deposits, where the rare earth elements (REE) occur adsorbed to clay mineral surfaces, are the world's dominant supply of heavy REE (Gd-Lu). These deposits are currently only mined in China where there is a reported heavy REE enrichment, but other deposits are currently under exploration in Brazil, the Philippines and Madagascar. Concentration of REE within IADs has been proposed to be a dominantly supergene process, where easily degradable REE-minerals (e.g. REE-fluorcarbonates) break down and release REE that are then adsorbed to clay minerals resulting in HREE enrichment. Here we present data from the Ambohimirahavavy Complex, Madagascar, and compare them to data from mineralised profiles in China, with the aim of further constraining the formation and REE enrichment processes in ion adsorption deposits. Bulk rock total REE contents from Madagascar vary from 400-5000ppm, with the HREE varying from 10 to 20% of the TREE. Ammonium Sulphate leaches (designed to remove clay-adsorbed REE) of laterite show leachable TREE from 130-500ppm, with no preferential HREE adsorption. Within the sequential extraction procedure the reducible fraction (hydroxylammonium chloride leach) showed the highest REE, but this is largely attributable to Ce4+ in oxide layers. Analysis of laterite profiles show that the REE distribution is heterogeneous, with control from both bedrock heterogeneity, and the hydrological variation between pedolith and saprolith. Similar patterns are seen in Chinese profiles from Jiangxi province. X-ray diffraction shows the clay fraction in all sites is dominated by kaolinite and halloysite. These data are consistent with experimental data which show that kaolinite is only HREE selective in high ionic strength solutions (Coppin et al., 2002), and suggest that HREE enrichment in lateritic deposits may be a function of exceptional bed rock conditions. Petrographic investigation of the Zhaibei granite, immediately underlying HREE enriched weathering profiles in Jiangxi province has identified the presence of HREE-enriched secondary phases associated with carbonate-rich areas (Xu et al., In press). Neodymium isotope data from primary granitic minerals (ɛNd(t)=-11.5±0.5) contrasts dramatically with data from HREE-enriched minerals (ɛNd(t)=0.9±0.8) indicating that pre-weathering metasomatism from fluids derived from outside the granite system may be critical in the HREE enrichment process of mineralised laterites. This may be important in determining the viability of ion adsorption deposits as HREE resources. Coppin et al. (2002) Sorption of lanthanides on smectite and kaolinite. Chem. Geol. 182, 57-68 Xu et al., (In press) Origin of heavy rare earth mineralization in South China. Nature Comms.
NASA Astrophysics Data System (ADS)
Dominika Dybowska, Agnieszka; Luciene Maltoni, Katia; Piella, Jordi; Najorka, Jens; Puntes, Victor; Valsami-Jones, Eugenia
2015-04-01
Stability and reactivity of minerals change as a particle size function, which makes mineral nanoparticles (defined here as <100 nm) fundamentally distinct from the larger size materials. Naturally occurring mineral nanoparticles contribute to many biogeochemical processes, however much remains to be learnt about these materials, their size dependent behavior and environmental significance. Advances in analytical, imaging and spectroscopic techniques made it now possible to study such particles; however we still have limited knowledge of their chemical, structural and morphological identity and reactivity, in particular in soils. The aim of this research was to characterize the naturally occurring nanoparticles in three soils from Brazil central region. The samples were collected in the A horizon, treated with H2O2 to remove organic material, dispersed in ultrasonic bath and wet sieved (53 µm) to remove the sand fraction. The clay fraction was collected by siphoning the supernatant, conditioned in 1000 ml cylinder, according to the Stock's law. This fraction was further processed by re-suspension in water, sonication and repeated centrifugation, to separate the fraction smaller than 100nm. This material, called here the soil "nanofraction", was analyzed using a range of techniques: 1) nanoparticle size/morphology and crystallinity with Transmission Electron Microscopy (TEM operateing in scanning (HAADF-STEM) and High Resolution (HRTEM) mode), 2) size distribution in water with Dynamic Light Scattering (DLS) and surface charge estimated from electrophoretic mobility measurements 3) crystal phase and crystallite size with X-ray Diffraction (XRD) 4) Chemical composition by quantitative analysis of elements (e.g., Si, Fe, Al, Ti) and their spatial distribution with HRTEM/EDS elemental mappings. The nanofraction had an average hydrodynamic particle diameter ranging from 83 to 92nm with a low polydispersity index of 0.13-0.17 and was found highly stable in aqueous suspension (no change in average particle size up to several months of storage). Particle surface charge (in water) ranged from -31mV to -34.5mV (pH = 5.7 - 6.2), this reflects the predominantly negative surface charge of kaolinites in soil environment effectively screening the positive charge of Fe oxides. Kaolinites appeared as single crystals (pseudo hexagonal platelets) while Fe oxides occurred mostly as micro-aggregates, with individual particles often not morphologically distinct with particle size <10nm. In addition, several anatase (TiO2) nanoparticles were also found. Both kaolinites and Fe oxides nanoparticles were crystalline, as evidenced from XRD measurements and HRTEM imaging. Distinction between different crystalline forms of Fe oxides (mainly hematite and goethite) was only possible with XRD, which revealed also subtle differences in mineralogical composition of the clay fraction (<2µm) and nanofraction (<100nm). The kaolinite's crystallite size (calculated from XRD data) was found to range 14-17nm in the nanofraction and 26-50nm in the clay fraction. For hematite, it was 13nm in the nanofraction and ranged from 21-30nm in the clay fraction. Such small particles can be expected to play an important role in soil sorption processes with implications on nutrient and contaminant cycling. Identification and understanding of the properties of naturally occurring nanoparticles in soils can therefore help soil scientists to better understand retention/mobilization of nutrients and pollutants in soils.
The use of fortified soil-clay as on-site system for domestic wastewater purification.
Oladoja, N A; Ademoroti, C M A
2006-02-01
The quest for simple, low-cost and high-performance decentralized wastewater treatment system for domestic application in developing nations necessitated this study. Clay samples collected from different deposits in Nigeria were characterized by studying the mineralogical and geochemical composition using X-ray diffraction (XRD) and atomic absorption spectroscopy (AAS), respectively. Three major clay minerals of kaolinite, illite and smectite were identified. The geochemical studies showed the abundance of SiO2, Al2O3 and H2O+ in each of the clay samples. Performance efficiency studies were conducted to determine the best combination ratio of pebbles/soil-clay. Soil-clay fortified by pebbles in combination ratios of 1:3 (i.e. pebbles:soil-clay = 1:3 (w/w) showed the optimum water purification, while the combination 3:1 gave the least. The flow rate studies showed that the wastewater had a longer residence time in non-fortified soil-clay than in fortified soil-clay. Two modes of treatment methods were employed-single and double column treatment methods (SCT and DCT). The two methods gave effluents of good quality characteristics, but those from the DCT were of better quality. The quality of effluents also varies from one clay type to another. The quality of effluents from media containing smectite clay mineral was better than those from other columns. Repeated usage of the fortified clay column showed a decrease of pH, TS and DO, and an increase of COD when monitored over a period of 10 days.
Timing and conditions of clay fault gouge formation on the Naxos detachment (Cyclades, Greece)
NASA Astrophysics Data System (ADS)
Mancktelow, N.; Zwingmann, H.; Mulch, A.
2016-10-01
Clay fault gouge from the Naxos detachment (locally up to 1.0-1.5 m thick) is reported and dated for the first time. K-Ar ages on eight clay size fractions from the detachment and a minor fault in the immediate footwall have a narrow range, from 10.3 to 9.0 Ma, with an average of 9.7 ± 0.5 Ma (±1σ). These results are in excellent accord with regional and local age constraints, independently demonstrating the reliability of the method. Hydrogen δD values fall in the range -89 to -95‰, indicating interaction with infiltrating meteoric water during gouge formation, which is consistent with deposition of freshwater sediments in the hanging wall at the same time. Clay mineralogy in the detachment gouge is predominantly mixed layer illite-smectite with subordinate 1 M illite and kaolinite but without higher-temperature 2 M1 illite/mica. Clay fault gouge predominantly formed over a limited time and temperature range, potentially acting as a weak lubricant promoting movement on the Naxos detachment, with correspondingly rapid exhumation and cooling of the underlying footwall.
The radiolysis and radioracemization of amino acids on clays
NASA Technical Reports Server (NTRS)
Bonner, W. A.; Hall, H.; Chow, G.; Yi, L.; Lemmon, R. M.
1985-01-01
The effects of the surfaces of kaolinite and bentonite clays on the radiolysis and radioracemization of L-leucine and its hydrochloride salt have been investigated experimentally. L-leucine and its hydrochloride salt were deposited on the clays and the amino acid/clay preparations were irradiated by a Co-60 gamma-ray source which induced 2-89 percent radiolysis. The efficiency of radiolysis and radioracemization were measured using gas chromatography. Results were obtained for leucine in 0.1 M aqueous solution for comparison with the clay-deposted leucine and leucine hydrochloride. It is found that radiolysis and radioracemization in the samples occurred according to a pseudo-first-order rate law. Comparison of the specific rate constants showed that leucine and its hydrochloride salt were the most resistant to both radiolysis and radioracemization, followed by leucine and its hydrochloride salt on kaolin. Leucine and its HCl salt on bentonite, and leucine in aqueous solution were found to be the least resistant to radiolysis and radioracemization. The experimental results are intepreted with respect to the Vester-Ulbricht mechanism for the origin of optical activity.
Installation Restoration Program Phase 2. Confirmation/Quantification. Stage 1. Volume 1.
1986-10-10
FIGUR 1- EEA LNO EFIG I AiNLanfl GUARD BASESHOWING PHSE II INVTIGTOIE I 1- ........ Site No. - I MAA Site No.Northwest Landfill TS Site.No.4 West...Protective Steel PVC Cap Flush Mount in Casing Plastic Nelson Valve Box Land Surface PVC Cap . Cement Grout 0 L n aBentonite Pellet 4" Diameter Seal...12.0 feet BLS. Clays of high plasticity predominate in all three wells. No sand lenses were encountered and the topsoil at all three well locations is
NASA Astrophysics Data System (ADS)
Shi, Xuefa; Liu, Shengfa; Fang, Xisheng; Qiao, Shuqing; Khokiattiwong, Somkiat; Kornkanitnan, Narumol
2015-06-01
A high density sampling program during two joint China-Thailand scientific cruises in 2011-2012 included collection of 152 gravity box cores in the Gulf of Thailand (GoT). Samples from the top 5 cm of each core were analyzed by X-ray diffraction for clay mineral content. Several systemic analytical approaches were applied to examine the distribution pattern and the constraint factors of clay minerals in the surface sediments of the western GoT. The clay minerals mainly comprise illite, kaolinite, chlorite and smectite, having the average weight percent distributions of 50%, 34%, 14% and 2%, respectively. Based on the spatial distribution characteristics and statistical results, the study area can be classified into three provinces. Province I contains high concentrations of smectite, and covers the northern GoT, sediments in this province are mainly from rivers discharging into the upper GoT, especially the Chao Phraya and Mae Klong Rivers. Sediments in Province II are characterized by higher values of illite, located in the central GoT, where fine sediments are contributed by the Mekong River and from the South China Sea. Province Ш, in the coastal regions of southwestern GoT close to Malaysia, exhibits a clay mineral assemblage with complex distribution patterns, and may contain terrestrial materials from the Mae Klong River as well as re-suspended sediments. Results of integrative analysis also demonstrate that the hydrodynamic environment in the study area, especially the seasonal various circumfluence and eddies, play an important role in the spatial distribution and dispersal of clay fraction in sediments.
Mineralogy and provenance of clays in miarolitic cavities of the Pikes Peak Batholith, Colorado
Kile, D.E.
2005-01-01
Clay samples from 105 cavities within miarolitic granitic pegmatites throughout the Pikes Peak batholith, in Colorado, were analyzed by powder X-ray diffraction (XRD). Smectite (beidellite), illite, and kaolinite were found within the cavities. Calculation of crystallite-thickness distribution (CTD), mean thickness of the crystallites, and variance in crystallite thickness, as deduced from XRD patterns, allowed a determination of provenance and mode of formation for illite and smectite. Authigenic miarolitic-cavity illite and smectite show lognormal CTDs and larger mean thicknesses of crystallites than do their soil-derived counterparts; non-lognormal illite in a cavity results from mixing of cavity and soil illite. Analysis of mean thickness and thickness variance shows that crystal growth of illite is initiated by a nucleation event of short duration, followed by surface-controlled kinetics. Crystallization of the miarolitic cavity clays is presumed to occur by neoformation from hydrothermal fluids. The assessment of provenance allows a determination of regional and local distributions of clay minerals in miarolitic cavities within the Pikes Peak batholith.
NASA Astrophysics Data System (ADS)
Tassongwa, Bernard; Eba, François; Njoya, Dayirou; Tchakounté, Jacqueline Numbem; Jeudong, Narcisse; Nkoumbou, Charles; Njopwouo, Daniel
2017-09-01
Field description and sampling along two pits, granulometry, Atterberg limits, mineralogical (XRD, FTIR, DSC & TGA) and geochemical analyses of the Balengou clays help to determine their characteristics and the genesis of the deposit. The mineralogical composition is comprised of halloysite-kaolinite, quartz, montmorillonite, hematite, anatase, feldspar, zircon, chromite, and apatite. Gibbsite and illite occur at the shallow and deep depth, respectively. Dikes of sand-poor clays contain also cristobalite and tridymite. Pairs of elements Rb-Ba, Rb-Sr, Nb-Ta, Ta-Zr, TiO2-Zr display good positive correlations (R2 > 0.85). REE patterns are highly fractionated (LaN up to 3312, LaN/YbN: 19-10) and are marked by deep Ce and Eu negative anomalies. Immobile element canonical ratios indicate that the protoliths were commendite/pantelerite, rhyolite and dacite, or their plutonic equivalents. Mineralogical and geochemical features lead to the suggestion that the clays derived from an advanced argillic hydrothermal alteration.
NASA Technical Reports Server (NTRS)
Izett, G. A.
1988-01-01
At 20 sites in the Raton Basin of Colorado and New Mexico, and at several other sites in Wyoming, Montana, and Canada, a pair of claystone units, an Ir abundance anomaly, and a concentration of shock-metamorphosed minerals mark the palynological K-T boundary. The K-T boundary claystone, which is composed of kaolinite and small amounts of illite/smectite mixed-layer clay, is similar in most respects to kaolinite tonstein layers in coal beds. At some, but not all, K-T boundary localities, the boundary claystone contains solid kaolinite and hollow and solid goyazite spherules, 0.05 to 1.2 mm in diameter. The upper unit, the K-T boundary impact layer, consists chiefly of kaolinite and various amounts of illite/smectite mixed-layer clay. The impact layer and boundary claystone are similar chemically, except that the former has slightly more Fe, K, Ba, Cr, Cu, Li, V, and Zn than the latter. The facts that the boundary claystone and impact layer contain anomalous amounts of Ir, comprise a stratigraphic couplet at Western North American sites, and form thin, discrete layers, similar to air-fall units (volcanic or impact), suggest that the claystone units are of impact origin. Significantly, the impact layer contains as much as 2 percent clastic mineral grains, about 30 percent of which contain multiple sets of shock lamellae. Only one such concentration of shocked minerals has been found near the K-T boundary. The type of K-T boundary shock-metamorphosed materials (quartzite and metaquartzite) in the impact layer and the lack of shock lamellae in quartz and feldspar of pumice lapilli and granitic xenoliths in air-fall pumice units of silicic tuffs, such as the Bishop Tuff, eliminate the possibility that the shock-metamorphosed minerals in the K-T impact layer are of volcanic origin. The global size distribution and abundance of shock-metamorphosed mineral grains suggest that the K-T impact occurred in North America.
Impact of clay minerals on sulfate-reducing activity in aquifers
Wong, D.; Suflita, J.M.; McKinley, J.P.; Krumholz, L.R.
2004-01-01
Previous studies have shown that sulfate-reduction activity occurs in a heterogeneous manner throughout the terrestrial subsurface. Low-activity regions are often observed in the presence of clay minerals. Here we report that clays inhibit sulfate reduction activity in sediments and in a pure culture of Desulfovibriovulgaris. Clay minerals including bentonite and kaolinite inhibited sulfate reduction by 70–90% in sediments. Intact clays and clay colloids or soluble components, capable of passing through a 0.2-µm filter, were also inhibitory to sulfate-reducing bacteria. Other adsorbent materials, including anion or cation exchangers and a zeolite, did not inhibit sulfate reduction in sediments, suggesting that the effect of clays was not due to their cation-exchange capacity. We observed a strong correlation between the Al2O3content of clays and their relative ability to inhibit sulfate reduction in sediments (r2 = 0.82). This suggested that inhibition might be a direct effect of Al3+ (aq) on the bacteria. We then tested pure aluminum oxide (Al2O3) and showed it to act in a similar manner to clay. As dissolved aluminum is known to be toxic to a variety of organisms at low concentrations, our results suggest that the effects of clay on sulfate-reducing bacteria may be directly due to aluminum. Thus, our experiments provide an explanation for the lack of sulfate-reduction activity in clay-rich regions and presents a mechanism for the effect.
The Influence of Abrasion on Martian Dust Grains: Evidence from a Study of Antigorite Grains
NASA Technical Reports Server (NTRS)
Bishop, Janice L.; Drief, Ahmed; Dyar, M. Darby
2003-01-01
Grinding was shown to greatly affect the structure and a number of properties of antigorite grains in a study by Drief and Nieto. Grinding is likely to influence the structure of most clay mineral grains and has been shown recently to influence the structure of kaolinite. The antigorite structure includes curved waves of layered silicate as shown by D dony et al.. Our study was performed in order to characterize in detail changes in the mineral grains resulting from grinding and to assess the influence of physical processes on clay minerals on the surface of Mars. This project includes a combination of SEM, reflectance spectroscopy and Moessbauer spectroscopy.
Laboratory-scale study of possible use of residual sludge from glass sand beneficiation
NASA Astrophysics Data System (ADS)
Prikryl, Richard; Weishauptova, Zuzana; Zach, Jaroslav; Kozlovcev, Petr
2016-04-01
Beneficiation of quartz sand from sedimentary deposits for glass sands results in significant amounts of under-size fraction, a sludge rich in clay minerals. This sludge is considered as a waste and is returned in mined-out spaces for a simple rehabilitation, which is also the case of one of the largest glass sand production areas in the Czech Republic. The amount of produced waste sludge in the studied area (glass sand works in Provodín area, Bohemian Cretaceous Basin) is about 20 kt per year. In the recent study, we have focused on possible employment of this waste material for three applications: (1) a clay component in a raw material mixture for making of hydraulic lime, (2) a kaolinite absorbent, and (3) a geotechnical material. The sampled sludge was primarily analysed for mineralogical and chemical composition, mechanical and physical properties, the specific surface area, and parameters of pore space. X-ray analysis proved the presence of kaolinite, illite (both WCI and PCI), quartz, and accessory microcline. According to silicate analysis, the material is composed of SiO2 (80.52 wt. %), Al2O3 (11.36 wt. %), and K2O (2.14 wt. %). For its potential use as an artificial admixture for hydraulic lime production, the studied material was mixed with pure limestone in ratio of 10, 15, 20, and/or 25 wt. %. The experimental mixtures were burnt in the temperature range from 850 to 1,200°C. XRD was employed for the detection of newly formed phases showing formation of hydraulic phase such as C2S, C3A, C4AF starting from the 1050°C burning temperature. Peak burning temperature significantly influenced amount of individual phases in the burnt product. Second possible mode of use of the investigated waste material focused on its application as a sorbent. Pore space and specific surface area characteristics (SBET 7.4 sq. m/g) range this material to the group of low grade kaolinite-dominated adsorbents. Thermal treatment (burning of raw waste material at temperatures of 500°C and/or 900°C) lead to rapid deterioration of specific surface area, probably due to the structural and phase changes of dominant clay minerals. The latest considered use in the field of geotechnical applications proved possible employment of the studied material as a sealing clay for smaller dams, ponds and/or as a geotechnical barrier for waste dumps.
Controlled Release of Active Agents using Inorganic Tubules.
1995-07-31
In a preferred embodiment, the hollow ceramic or inorganic microtubule is a mineral 11 microtubule, such as halloysite , cylindrite, boulangerite, or...19 common of these is halloysite , an inorganic aluminosilicate belonging to the kaolinite group 20 of clay minerals. See generally, Bates et al...34Morphology and structure of endellite and 21 halloysite ", American Minerologists 35 463-85 (1950), which remains the definitive paper on 7 Navy Case No
Fluoride content of clay minerals and argillaceous earth materials
Thomas, Josephus; Glass, H.D.; White, W.A.; Trandel, R.M.
1977-01-01
A reliable method, utilizing a fluoride ion-selective electrode, is described for the determination of fluoride in clays and shales. Interference by aluminum and iron is minimal. The reproducibility of the method is about ±5% at different levels of fluoride concentration.Data are presented for various clay minerals and for the <2-µm fractions of marine and nonmarine clays and shales. Fluoride values range from 44 ppm (0.0044%) for nontronite from Colfax, WA, to 51,800 ppm (5.18%) for hectorite from Hector, CA. In general, clays formed under hydrothermal conditions are relatively high in fluoride content, provided the hydrothermal waters are high in fluoride content. Besides hectorite, dickite from Ouray, CO, was found to contain more than 50 times as much fluoride (6700 ppm) as highly crystalline geode kaolinite (125 ppm). The clay stratum immediately overlying a fluorite mineralized zone in southern Illinois was found to have a higher fluoride content than the same stratum in a nonmineralized zone approximately 1 mile away. Nonmarine shales in contact with Australian coals were found to be lower in fluoride content than were marine shales in contact with Illinois coals.It is believed that, in certain instances, peak shifts on DTA curves of similar clay minerals are the result of significant differences in their fluoride content.
Sand and clay mineralogy of sal forest soils of the Doon Siwalik Himalayas
NASA Astrophysics Data System (ADS)
Mukesh; Manhas, R. K.; Tripathi, A. K.; Raina, A. K.; Gupta, M. K.; Kamboj, S. K.
2011-02-01
The peteromineralogical characterization of the soil was carried out for the 12 soil profiles exposed in the Shorea robusta dominated forests of the Siwalik forest division, Dehradun. The quartz was observed as the dominating light mineral fraction (64-80%) in all the profiles studied. Biotite, hornblende, zircon, tourmaline, rutile and opaques comprising of iron minerals constituted the heavy mineral fraction (20%). The mineralogy of both the sand and clay fractions revealed a mixed mineralogy. The clay minerals in the order of their dominance were vermiculite, illite, kaolinite and mixed layer minerals. The presence of vermiculite and illite in appreciable quantities indicates that these were synthesized from the K-rich soil solution, as orthoclase and micas were present in significant quantities in the sand minerals. The mineral suites identified in the study shows that the geological, climatological and topographical factors of the region collectively played a dominant role in their formation and transformation. After critical appraisal of the results, it may be deduced that the mineralogical composition, physicochemical properties and total elemental analysis of the soils do not show any deficiency of the bases and other plant nutrients in general. The inherent fertility of the soil is good as indicated by the sand and clay mineralogy of the soil and the biotite and feldspar together with the mica is an important source of nutrients for the vegetation in the soils of the Doon valley.
NASA Astrophysics Data System (ADS)
Stipp, Michael; Schumann, Kai; Leiss, Bernd; Ullemeyer, Klaus
2014-05-01
The Nankai Trough Seismogenic Zone Experiment of the International Ocean Discovery Program (IODP) is the very first attempt to drill into the seismogenic part of a subduction zone. Offshore SW-Japan the oceanic Philippine sea plate is subducted beneath the continental Eurasian plate causing earthquakes of magnitude 8.0 to 8.5 and related tsunamis with a recurrence rate of 80-100 years. For the tsunamigenic potential of the forearc slope and accreted sediments their mechanical strength, composition and fabrics have been investigated. 19 drill core samples of IODP Expeditions 315, 316 and 333 were experimentally deformed in a triaxial cell under consolidated and undrained conditions at confining pressures of 400-1000 kPa, room temperature, axial shortening rates of 0.01-9.0 mm/min, and up to an axial strain of ˜64% (Stipp et al., 2013). With respect to the mechanical behavior, two distinct sample groups could be distinguished. Weak samples from the upper and middle forearc slope of the accretionary prism show a deviatoric peak stress after only a few percent strain (< 10%) and a continuous stress decrease after a maximum combined with a continuous increase in pore pressure. Strong samples from the accretionary prism toe display a constant residual stress at maximum level or even a continuous stress increase together with a decrease in pore pressure towards high strain (Stipp et al., 2013). Synchrotron texture and composition analysis of the experimentally deformed and undeformed samples using the Rietveld refinement program MAUD indicates an increasing strength of the illite and kaolinite textures with increasing depth down to 523 m below sea floor corresponding to a preferred mineral alignment due to compaction. Experimentally deformed samples have generally stronger textures than related undeformed core samples and they show also increasing strength of the illite and kaolinite textures with increasing axial strain. Mechanically weak samples have a bulk clay plus calcite content of 31-65 vol.-% and most of their illite, kaolinite, smectite and calcite [001]-pole figures have maxima >1.5 mrd. Strong samples which were deformed to approximately the same amount of strain (up to 40%) have no calcite and a bulk clay content of 24-36 vol.-%. Illite, kaolinite and smectite [001]-pole figure maxima are mostly <1.5 mrd, except for one sample which was deformed to a considerably higher strain (64%). The higher clay and calcite content and the stronger textures of the mechanically weak samples can be related to a collapsing pore space of the originally flocculated clay aggregates. This process is insignificant in the strong samples from the prism toe, for which deformation would tend to involve large rock volumes and lead to strain dissipation. The weak samples from the forearc slope which become even weaker with increasing strain may provoke mechanical runaway situations allowing for earthquake rupture, surface breakage and tsunami generation. Stipp, M., Rolfs, M., Kitamura, Y., Behrmann, J.H., Schumann, K., Schulte-Kortnack, D. and Feeser, V. 2013. G-Cubed 14/11, doi: 10.1002/ggge.20290.
Unuabonah, Emmanuel I; Olu-Owolabi, Bamidele I; Fasuyi, Esther I; Adebowale, Kayode O
2010-07-15
Kaolinite clay was treated with polyvinyl alcohol to produce a novel water-stable composite called polymer-clay composite adsorbent. The modified adsorbent was found to have a maximum adsorption capacity of 20,400+/-13 mg/L (1236 mg/g) and a maximum adsorption rate constant of approximately = 7.45x10(-3)+/-0.0002 L/(min mg) at 50% breakthrough. Increase in bed height increased both the breakpoint and exhaustion point of the polymer-clay composite adsorbent. The time for the movement of the Mass Transfer Zone (delta) down the column was found to increase with increasing bed height. The presence of preadsorbed electrolyte and regeneration were found to reduce this time. Increased initial Cd(2+) concentration, presence of preadsorbed electrolyte, and regeneration of polymer-clay composite adsorbent reduced the volume of effluent treated. Premodification of polymer-clay composite adsorbent with Ca- and Na-electrolytes reduced the rate of adsorption of Cd(2+) onto polymer-clay composite and lowered the breakthrough time of the adsorbent. Regeneration and re-adsorption studies on the polymer-clay composite adsorbent presented a decrease in the bed volume treated at both the breakpoint and exhaustion points of the regenerated bed. Experimental data were observed to show stronger fits to the Bed Depth Service Time (BDST) model than the Thomas model. 2010 Elsevier B.V. All rights reserved.
NASA Astrophysics Data System (ADS)
Preziosi-Ribero, A.; Fox, A.; Packman, A. I.; Escobar-Vargas, J.; Donado-Garzon, L. D.; Li, A.; Arnon, S.
2017-12-01
Exchange of mass, momentum and energy between surface water and groundwater is a driving factor for the biology, ecology and chemistry of rivers and water bodies in general. Nonetheless, this exchange is dominated by different factors like topography, bed morphology, and large-scale hydraulic gradient. In the particular case of fine sediments like clay, conservative tracer modeling is impossible because they are trapped in river beds for long periods, thus the normal advection dispersion approach leads to errors and results do not agree with reality. This study proposes a numerical particle tracking model that represents the behavior of kaolinite in a sand flume, and how its deposition varies according to different flow conditions, namely losing and gaining flow. Since fine particles do not behave like solutes, kaolinite dynamics are represented using settling velocity and a filtration coefficient allowing the particles to be trapped in the bed. This approach allows us to use measurable parameters directly related with the fine particle features as size and shape, and hydraulic parameters. Results are then compared with experimental results from lab experiments obtained in a recirculating flume, in order to assess the impact of losing and gaining conditions on sediment transport and deposition. Furthermore, our model is able to identify the zones where kaolinite deposition concentrates over the flume due to the bed geometry, and later relate these results with clogging of the bed and hence changes in the bed's hydraulic conductivity. Our results suggest that kaolinite deposition is higher under losing conditions since the vertical velocity of the flow is added to the deposition velocity of the particles modeled. Moreover, the zones where kaolinite concentrates varies under different flow conditions due to the difference in pressure and velocity in the river bed.
NASA Astrophysics Data System (ADS)
Bonaccorsi, R.; McKay, C. P.
2009-12-01
Landing sites of next missions to Mars i.e., the US 2011 Mars Science Laboratory (MSL11) and the ESA2016 Pasteur ExoMars, will include phyllosilicate outcrops as targets for investigating the geological and biological history of that planet. In this context, we present a study assessing the living biomass and habitability potential in mineralogical Mars analogs such as phyllosilicates and hematite-rich deposits encompassing a broad arid-hyper-arid climate range (annual rainfall <0.2 to ~700mm/y). Samples from the Atacama Desert (Chile), the Death Valley (CA), and the California Coast (USA) were analyzed for microbial lipopolysaccharide (LPS) as proxy for Gram-negatives biomass with the Limulus-Amebocite-Lysate (LAL) assay. Mineral phases were identified using X-Ray-Diffraction (XRD). These samples resulted to contain phyllosilicate phases similar to those identified, or inferred [1], on the surface of Mars by the OMEGA-Mars/Express [e.g., 2], the Mars Reconnaissance Orbiter (MRO) instruments (HiRISE and CRISM) [3]. Basic observations were: 1) there is no systematic pattern in biomass content of clays vs. non-clays (oxidized) materials from the study sites; 2) Atacama desiccation polygons (muscovite and kaolinite) and contiguous hematite-rich hyper-arid deposits contain the lowest biomass, i.e., ~104to-105 cells/g, respectively; 3) the hyper-arid clays contain three-order magnitude lower Gram-negative biomass than those (montmorillonite, illite, and chlorite) from the arid Death Valley site (~107cells/g); and 4) finally, the Gram-negative (~107cells/g) of clay minerals-rich materials from the arid site is about the same than that (~1.5 to ~3.0 x 107cells/g) of water-saturated massive deposits (kaolinite, illite, and vermiculite) from the wetter California coast. Results from this investigation will help testing for the habitability potential of phyllosilicate deposits sampled by the MSL11 Mission. REFERENCES:[1] Bibring et al., 2006, Science 312:400-404; [2] Wang et al., 2006 JGR E02S16 Vol.111; [3] Bishop et al., 2008. Science, 321,830-833.
Herich, Hanna; Tritscher, Torsten; Wiacek, Aldona; Gysel, Martin; Weingartner, Ernest; Lohmann, Ulrike; Baltensperger, Urs; Cziczo, Daniel J
2009-09-28
Airborne mineral dust particles serve as cloud condensation nuclei (CCN), thereby influencing the formation and properties of warm clouds. It is therefore of atmospheric interest how dust aerosols with different mineralogy behave when exposed to high relative humidity (RH) or supersaturation (SS) with respect to liquid water. In this study the subsaturated hygroscopic growth and the supersaturated cloud condensation nucleus activity of pure clays and real desert dust aerosols were determined using a hygroscopicity tandem differential mobility analyzer (HTDMA) and a cloud condensation nuclei counter (CCNC), respectively. Five different illite, montmorillonite and kaolinite clay samples as well as three desert dust samples (Saharan dust (SD), Chinese dust (CD) and Arizona test dust (ATD)) were investigated. Aerosols were generated both with a wet and a dry disperser. The water uptake was parameterized via the hygroscopicity parameter kappa. The hygroscopicity of dry generated dust aerosols was found to be negligible when compared to processed atmospheric aerosols, with CCNC derived kappa values between 0.00 and 0.02 (the latter corresponds to a particle consisting of 96.7% by volume insoluble material and approximately 3.3% ammonium sulfate). Pure clay aerosols were generally found to be less hygroscopic than natural desert dust particles. The illite and montmorillonite samples had kappa approximately 0.003. The kaolinite samples were less hygroscopic and had kappa=0.001. SD (kappa=0.023) was found to be the most hygroscopic dry-generated desert dust followed by CD (kappa=0.007) and ATD (kappa=0.003). Wet-generated dust showed an increased water uptake when compared to dry-generated samples. This is considered to be an artifact introduced by redistribution of soluble material between the particles. Thus, the generation method is critically important when presenting such data. These results indicate any atmospheric processing of a fresh mineral dust particle which leads to the addition of more than approximately 3% soluble material will significantly enhance its hygroscopicity and CCN activity.
Coupled Viscous Fluid Flow and Joint Deformation Analysis for Grout Injection in a Rock Joint
NASA Astrophysics Data System (ADS)
Kim, Hyung-Mok; Lee, Jong-Won; Yazdani, Mahmoud; Tohidi, Elham; Nejati, Hamid Reza; Park, Eui-Seob
2018-02-01
Fluid flow modeling is a major area of interest within the field of rock mechanics. The main objective of this study is to gain insight into the performance of grout injection inside jointed rock masses by numerical modeling of grout flow through a single rock joint. Grout flow has been widely simulated using non-Newtonian Bingham fluid characterized by two main parameters of dynamic viscosity and shear yield strength both of which are time dependent. The increasing value of these properties with injection time will apparently affect the parameters representing the grouting performance including grout penetration length and volumetric injection rate. In addition, through hydromechanical coupling a mutual influence between the injection pressure from the one side and the joint opening/closing behavior and the aperture profile variation on the other side is anticipated. This is capable of producing a considerable impact on grout spread within the rock joints. In this study based on the Bingham fluid model, a series of numerical analysis has been conducted using UDEC to simulate the flow of viscous grout in a single rock joint with smooth parallel surfaces. In these analyses, the time-dependent evolution of the grout fluid properties and the hydromechanical coupling have been considered to investigate their impact on grouting performance. In order to verify the validity of these simulations, the results of analyses including the grout penetration length and the injection flow rate were compared with a well-known analytical solution which is available for the simple case of constant grout properties and non-coupled hydraulic analysis. The comparison demonstrated that the grout penetration length can be overestimated when the time-dependent hardening of grout material is not considered. Moreover, due to the HM coupling, it was shown that the joint opening induced by injection pressure may have a considerable increasing impression on the values of penetration length and injected grout volume.
Silicate-catalyzed chemical grouting compositions
DOE Office of Scientific and Technical Information (OSTI.GOV)
Not Available
1972-09-28
Chemical grouting compositions for stabilizing earth, sand, and other porous particulate formations or agglomerates of solids are described. The composition for producing a chemically grouting structure consists of an aqueous base solution of: (1) vegetative polyphenolic material consisting of condensed type tannins, and an aqueous catalyst solution of (2) a water-soluble alkali metal silicate. The polyphenolic material is present in an amount from 5% to 40% based on the weight of the base solution, and the water- soluble alkali metal silicate is present in an amount to provide from 1% to 15% SiOD2U in the silicate compound based on themore » weight of the polyphenolic material. These grouting compositions are completely safe to operating personnel and to surrounding environment, since the potassium or sodium silicate catalysts are nontoxic. (15 claims)« less
An Efficient Method for Subsurface Treatments, Including Squeeze Treatments
2000-03-03
microstructures suitable for use in the present invention. The most common of these is halloysite , an inorganic aluminosilicate belonging to the kaolinite group...of clay minerals. See generally, Bates et al., "Morphology and structure of endellite and halloysite ", American 20 Minerologists 35 463-85...1950), which remains the definitive paper on halloysite . The mineral has 10 10 15 SSSn^.a,. PATHNTAPPHCATION the chemical formula Al203-2Si02
Adsorption coefficients for TNT on soil and clay minerals
NASA Astrophysics Data System (ADS)
Rivera, Rosángela; Pabón, Julissa; Pérez, Omarie; Muñoz, Miguel A.; Mina, Nairmen
2007-04-01
To understand the fate and transport mechanisms of TNT from buried landmines is it essential to determine the adsorption process of TNT on soil and clay minerals. In this research, soil samples from horizons Ap and A from Jobos Series at Isabela, Puerto Rico were studied. The clay fractions were separated from the other soil components by centrifugation. Using the hydrometer method the particle size distribution for the soil horizons was obtained. Physical and chemical characterization studies such as cation exchange capacity (CEC), surface area, percent of organic matter and pH were performed for the soil and clay samples. A complete mineralogical characterization of clay fractions using X-ray diffraction analysis reveals the presence of kaolinite, goethite, hematite, gibbsite and quartz. In order to obtain adsorption coefficients (K d values) for the TNT-soil and TNT-clay interactions high performance liquid chromatography (HPLC) was used. The adsorption process for TNT-soil was described by the Langmuir model. A higher adsorption was observed in the Ap horizon. The Freundlich model described the adsorption process for TNT-clay interactions. The affinity and relative adsorption capacity of the clay for TNT were higher in the A horizon. These results suggest that adsorption by soil organic matter predominates over adsorption on clay minerals when significant soil organic matter content is present. It was found that, properties like cation exchange capacity and surface area are important factors in the adsorption of clayey soils.
Ramasamy, V; Paramasivam, K; Suresh, G; Jose, M T
2014-01-03
Using Gamma ray and Fourier Transform Infrared (FTIR) spectroscopic techniques, level of natural radioactivity ((238)U, (232)Th and (40)K) and mineralogical characterization of Vaigai River sediments have been analyzed with the view of evaluating the radiation risk and its relation to available minerals. Different radiological parameters are calculated to know the entire radiological characterization. The average of activity concentrations and all radiological parameters are lower than the recommended safety limit. However, some sites are having higher radioactivity values than the safety limit. From the FTIR spectroscopic technique, the minerals such as quartz, microcline feldspar, orthoclase feldspar, kaolinite, gibbsite, calcite, montmorillonite and organic carbon are identified and they are characterized. The extinction co-efficient values are calculated to know the relative distribution of major minerals such as quartz, microcline feldspar, orthoclase feldspar and kaolinite. The calculated values indicate that the amount of quartz is higher than orthoclase feldspar, microcline feldspar and much higher than kaolinite. Crystallinity index is calculated to know the crystalline nature of quartz and the result indicates that the presence of ordered crystalline quartz in the present sediment. The role of minerals in the level of radioactivity is assessed by multivariate statistical analysis (Pearson's correlation and Cluster analysis). The statistical analysis confirms that the clay mineral kaolinite is the major factor than other major minerals to induce the important radioactivity variables such as absorbed dose rate and concentrations of (232)Th and (238)U. Copyright © 2013 Elsevier B.V. All rights reserved.
NASA Astrophysics Data System (ADS)
Kent, Dennis V.; Lanci, Luca; Wang, Huapei; Wright, James D.
2017-09-01
The kaolinite-rich Marlboro Clay was deposited on the inner shelf in the Salisbury Embayment of the U.S. Atlantic margin at the onset of the carbon isotope excursion marking the 56 Ma Paleocene-Eocene boundary and is characterized by an anomalously high concentration of magnetic nanoparticles of enigmatic origin that give rise to notably intense bulk magnetization. Recent studies point to a magnetic assemblage that is dominated by single-domain magnetite particles that tend to be isolated rather than arranged in chains, the most distinguishing feature of magnetotactic bacteria fossils. On the other hand, it is very unlikely that the nanoparticles can be condensates of an impact plume given the meter-scale thickness of the Marlboro Clay. We obtained new data from a landward proximal site at Wilson Lake on the New Jersey Coastal Plain and find that the abrupt increase in magnetite nanoparticles is virtually coincident stratigraphically with the recently reported impact spherule layer at the base of the Marlboro Clay in the same core. Yet the high field magnetic susceptibility, a measure of total iron concentration, and strontium isotope values on bulk sediment, an indicator of sediment weathering provenance, are not different in the Marlboro Clay from the immediately underlying Vincentown Formation. We suggest that the distinctive magnetic properties of the Marlboro Clay originated from pyromagnetic soil enhancement by widespread wildfires on the adjoining drainage area. The pyrogenetic products were soon washed from the denuded landscape and rapidly deposited as mud-waves across the shelf, becoming the Marlboro Clay. A few percent of incinerated biomass ends up as calcite known as wood ash stone and can inherit its light carbon isotope composition. Disseminated wood ash stone entrained in the Marlboro Clay could contribute to the landward increase in amplitude of the carbon isotope excursion in bulk carbonate data. A plausible trigger for the initial conflagration is a fireball from the impact of a sizable extraterrestrial object at moderate range.
Satellite-derived mineral mapping and monitoring of weathering, deposition and erosion
Cudahy, Thomas; Caccetta, Mike; Thomas, Matilda; Hewson, Robert; Abrams, Michael; Kato, Masatane; Kashimura, Osamu; Ninomiya, Yoshiki; Yamaguchi, Yasushi; Collings, Simon; Laukamp, Carsten; Ong, Cindy; Lau, Ian; Rodger, Andrew; Chia, Joanne; Warren, Peter; Woodcock, Robert; Fraser, Ryan; Rankine, Terry; Vote, Josh; de Caritat, Patrice; English, Pauline; Meyer, Dave; Doescher, Chris; Fu, Bihong; Shi, Pilong; Mitchell, Ross
2016-01-01
The Earth’s surface comprises minerals diagnostic of weathering, deposition and erosion. The first continental-scale mineral maps generated from an imaging satellite with spectral bands designed to measure clays, quartz and other minerals were released in 2012 for Australia. Here we show how these satellite mineral maps improve our understanding of weathering, erosional and depositional processes in the context of changing weather, climate and tectonics. The clay composition map shows how kaolinite has developed over tectonically stable continental crust in response to deep weathering during northwardly migrating tropical conditions from 45 to 10 Ma. The same clay composition map, in combination with one sensitive to water content, enables the discrimination of illite from montmorillonite clays that typically develop in large depositional environments over thin (sinking) continental crust such as the Lake Eyre Basin. Cutting across these clay patterns are sandy deserts that developed <10 Ma and are well mapped using another satellite product sensitive to the particle size of silicate minerals. This product can also be used to measure temporal gains/losses of surface clay caused by periodic wind erosion (dust) and rainfall inundation (flood) events. The accuracy and information content of these satellite mineral maps are validated using published data. PMID:27025192
NASA Astrophysics Data System (ADS)
Shi, Yaokun; Luo, Mingzhang; Li, Weijie; Song, Gangbing
2018-05-01
The concrete-filled fiber-reinforced polymer tube (CFFT) is a type of structural element widely used in corrosive environments. Poor grout compactness results in incomplete contact or even no contact between the fiber-reinforced polymer (FRP) tube and the concrete grout, which reduces the load bearing capacity of a CFFT. The monitoring of grout compactness for CFFTs is important. The piezoceramic-based electromechanical impedance (EMI) method has emerged as an efficient and low-cost structural health monitoring technique. This paper presents a feasibility study using the EMI method to monitor grout compactness of CFFTs. In this research, CFFT specimens with different levels of compactness (empty, 1/5, 1/3, 1/2, 2/3, and full compactness) were prepared and subjected to EMI measurement by using four piezoceramic patches that were bonded circumferentially along the outer surface of the CFFT. To analyze the correlation between grout compactness and EMI signatures, a compactness index (CI) was proposed based on the root-mean-square deviation (RMSD). The experimental results show that the changes in admittance signatures are able to determine the grout compactness qualitatively. The proposed CI is able to effectively identify the compactness of the CFFT, and provides location information of the incomplete concrete infill.
Effect of Acid on Surface Hydroxyl Groups on Kaolinite and Montmorillonite
DOE Office of Scientific and Technical Information (OSTI.GOV)
Sihvonen, Sarah K.; Murphy, Kelly A.; Washton, Nancy M.
Mineral dust aerosol participates in heterogeneous chemistry in the atmosphere. In particular, the hydroxyl groups on the surface of aluminosilicate clay minerals are important for heterogeneous atmospheric processes. These functional groups may be altered by acidic processing during atmospheric transport. In this study, we exposed kaolinite (KGa-1b) and montmorillonite (STx-1b) to aqueous sulfuric acid and then rinsed the soluble reactants and products off in order to explore changes to functional groups on the mineral surface. To quantify the changes due to acid treatment of edge hydroxyl groups, we use 19F magic angle spinning nuclear magnetic resonance spectroscopy and a probemore » molecule, 3,3,3-trifluoropropyldimethylchlorosilane. We find that the edge hydroxyl groups (OH) increase in both number and density with acid treatment. Chemical reactions in the atmosphere may be impacted by the increase in OH at the mineral edge.« less
NASA Astrophysics Data System (ADS)
Ramos, Yuddy; Goïta, Kalifa; Péloquin, Stéphane
2016-04-01
This study evaluates Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) and Hyperion hyperspectral sensor datasets to detect advanced argillic minerals. The spectral signatures of some alteration clay minerals, such as dickite and alunite, have similar absorption features; thus separating them using multispectral satellite images is a complex challenge. However, Hyperion with its fine spectral bands has potential for good separability of features. The Spectral Angle Mapper algorithm was used in this study to map three advanced argillic alteration minerals (alunite, kaolinite, and dickite) in a known alteration zone in the Peruvian Andes. The results from ASTER and Hyperion were analyzed, compared, and validated using a Portable Infrared Mineral Analyzer field spectrometer. The alterations corresponding to kaolinite and alunite were detected with both ASTER and Hyperion (80% to 84% accuracy). However, the dickite mineral was identified only with Hyperion (82% accuracy).
Water and Sediment Quality in the Yukon River Basin, Alaska, During Water Year 2005
2007-01-01
Disordered Kaolinite 0.6 0.5 0.4 0.7 0.6 1.0 0.4 Ferruginous smectite 7.4 9.5 6.1 4.9 9.4 10.6 12.4 Illite + Smectite 6.8 4.8 5.2 6.6 6.6 5.5 4.9...64.7 Clays: Goethite 0.1 0.1 0.3 0.1 0.1 0.3 0.1 Disordered Kaolinite 0.6 0.9 0.3 0.7 0.9 0.6 0.7 Ferruginous smectite 7.0 6.8 7.1...7.9 7.6 16.4 15.7 Illite + Smectite 10.2 7.7 8.1 7.9 6.8 1.2 3.2 Chlorite 8.0 9.5 9.6 9.4 10.7 10.8 12.2 Muscovite (2M1) 4.1 6.0 5.2 4.8 4.1 4.8
Diagenetic evaluation of Pannonian lacustrine deposits in the Makó Trough, southeastern Hungary
NASA Astrophysics Data System (ADS)
Szőcs, Emese; Milovský, Rastislav; Gier, Susanne; Hips, Kinga; Sztanó, Orsolya
2017-04-01
The Makó Trough is the deepest sub-basin of the Pannonian Basin. As a possible shale gas and tight gas accumulation the area was explored by several hydrocarbon companies. In this study, we present the preliminary results on the diagenetic history and the porosity evolution of sandstones and shales. Petrographic (optical microscopy, CL, blue light microscopy) and geochemical methods (SEM-EDX, WDX, O and C stable isotopes) were applied on core samples of Makó-7 well (3408- 5479 m). Processes which influenced the porosity evolution of the sandstones were compaction, cementation, mineral replacement and dissolution. The most common diagenetic minerals are carbonates (non-ferroan and Fe-bearing calcite, dolomite and ankerite), clay minerals (kaolinite, mixed layer illite-smectite and chlorite) and other silicates (quartz and feldspar). Initial clay mineral and ductile grain content also influences reservoir quality. The volumetrically most significant diagenetic minerals are calcite and clay minerals. The petrography of calcite is variable (bright orange to dull red luminescence color, pore-filling cement, replacive phases which are occasionally scattered in the matrix). The δ13 C-PDB values of calcite range from 1.7 ‰ to -5.5 ‰, while δ18 O-PDB values range from 0.5 ‰ to -9.1 ‰, no depth related trend was observed. These data suggest that calcite occurs in more generations, i.e. eogenetic pre-compactional and mesogenetic post-compactional. Kaolinite is present in mottles in size similar to detrital grains, where remnants of feldspars can be seen. This indicates feldspar alteration via influx of water rich in organic derived carbon dioxide. Secondary porosity can be observed in carbonates and feldspars at some levels, causing the improvement of the reservoir quality.
Evolution of soils on quaternary reef terraces of Barbados, West Indies
Muhs, D.R.
2001-01-01
Soils on uplifted Quaternary reef terraces of Barbados, ???125,000 to ???700,000 yr old, form a climo-chronosequence and show changes in physical, chemical, and mineralogical properties with terrace age. Parent materials are dust derived from the Sahara, volcanic ash from the Lesser Antilles island arc, and detrital carbonate from the underlying reef limestone. Although some terrace soils are probably eroded, soils or their remnants are redder and more clay-rich with increasing terrace age. Profile-average Al2O3 and Fe2O3 content increases with terrace age, which partially reflects the increasing clay content, but dithionite-extractable Fe also increases with terrace age. Profile-average K2O/TiO2, Na2O/TiO2, and P2O5/TiO2 values decrease with terrace age, reflecting the depletion of primary minerals. Average SiO2/Al2O3 values also decrease with terrace age and reflect not only loss of primary minerals but also evolution of secondary clay minerals. Although they are not present in any of the parent materials, the youngest terrace soils are dominated by smectite and interstratified kaolinite-smectite, which gradually alter to relatively pure kaolinite over ???700,000 yr. Comparisons with other tropical islands, where precipitation is higher and rates of dust fall may be lower, show that Barbados soils are less weathered than soils of comparable age. It is concluded that many soil properties in tropical regions can be potentially useful relative-age indicators in Quaternary stratigraphic studies, even when soils are eroded or changes in soil morphology are not dramatic. ?? 2001 University of Washington.
NASA Astrophysics Data System (ADS)
Fonseca, Rita M. F.; Barriga, Fernando J. A. S.; Conceição, Patrícia I. S. T.
2010-12-01
The Southern region of Portugal is subjected to several forms of over-erosion. Most leached products, mainly composed of fine particles containing nutrients, metals or pesticides, are easily transported by river flows. When these are hindered by a physical barrier such as a dam, the particulate load accumulates on the bottom of the reservoirs, often leading to a pronounced decrease of water quality. Bottom sediments from three reservoirs were subjected to grain-size analysis and a study of clay minerals by X-ray diffraction. Most sediments contain a diverse set of clay minerals, mostly illites, smectites, chlorites and kaolinites. The nature of the clay minerals reflects the nature of the parent rocks. During the cycles of transport and temporary deposition, they may undergo significant chemical and physical transformations, which lead to an increase of expandable properties and therefore, to a higher cationic exchange capacity, determining its important role as vehicles of environmental pollutants.
Formation of mixed-layer structures in smectites intercalated with tryptone
NASA Astrophysics Data System (ADS)
Block, K. A.; Trusiak, A.; Steiner, J. C.; Katz, A.; Gottlieb, P.; Alimova, A.
2012-12-01
Stable clay-protein complexes are fundamental to studies of the critical zone, terrestrial ecosystems, pharmacology, and industrial applications such as bioremediation. Two sets of montmorillonite clays were purified and made homoionic for Na and Mg. Mg-montmorillonite and Na-montmorillonite were mixed with tryptone (casein digest) in a 9:1 and 18:1 clay:tryptone ratio, resulting in the formation of reversible intercalated structures. X-ray diffraction analysis of the protein-clay complexes produced profiles consisting of two peaks associated with the smectite 001 reflection and a related tryptone-packet peak similar to that produced by a mixed layer clay structure. Shifts in the 002, 003, and 004 diffraction maxima are attributed to disorder caused by the interaction with the protein. Line broadening in the smectite-tryptone XRD spectra is interpreted to be the result of interlayer absorption. Adsorption produces coherent crystalline packets of regularly interbedded tryptone and smectite platelets. SEM images reveal clay platelets with upwardly rolled edges that tend toward cylindrical structures with the production of occasional tubes in the smaller platelet size range as noted for organic compound-kaolinite intercalation reported by Fenoll Hach-Ali and Weiss (1969). Reference: Fenoll Hach-Ali, P.F., Weiss, A., 1969. Estudio de la reaccion de caolinita y N-metilform- amida. Quimica LXV, 769-790. Scanning electron micrograph of tryptone-intercalated clay platelets exhibiting rolled edge structure.
Decomposition of algal lipids in clay-enriched marine sediment under oxic and anoxic conditions
NASA Astrophysics Data System (ADS)
Lü, Dongwei; Song, Qian; Wang, Xuchen
2010-01-01
A series of laboratory incubation experiments were conducted to examine the decomposition of algal organic matter in clay-enriched marine sediment under oxic and anoxic conditions. During the 245-day incubation period, changes in the concentrations of TOC, major algal fatty acid components (14:0, 16:0, 16:1, 18:1 and 20:5), and n-alkanes (C16-C23) were quantified in the samples. Our results indicate that the organic matters were degraded more rapidly in oxic than anoxic conditions. Adsorption of fatty acids onto clay minerals was a rapid and reversible process. Using a simple G model, we calculated the decomposition rate constants for TOC, n-alkanes and fatty acids which ranged from 0.017-0.024 d-1, 0.049-0.103 d-1 and 0.011 to 0.069 d-1, respectively. Algal organic matter degraded in two stages characterized by a fast and a slow degradation processes. The addition of clay minerals montmorillonite and kaolinite to the sediments showed significant influence affecting the decomposition processes of algal TOC and fatty acids by adsorption and incorporation of the compounds with clay particles. Adsorption/association of fatty acids by clay minerals was rapid but appeared to be a slow reversible process. In addition to the sediment redox and clay influence, the structure of the compounds also played important roles in affecting their degradation dynamic in sediments.
Infrared detection of the mineralogical aspects that influence the processing of calcined kaolin
NASA Astrophysics Data System (ADS)
Groenheide, Stefan; Guatame-Garcia, Adriana; Buxton, Mike; van der Werff, Harald
2017-04-01
Calcined kaolin is an industrial minerals product used in the production of paper, paint, rubber and other specialty applications. It is produced from kaolinite through a series of refinement steps and final calcination at temperatures of above 900°C, with the aim of generating a whiter and more abrasive material. The raw kaolin ore is a mixture of clay minerals, quartz and feldspars, where kaolinite is the main constituent. The optimal kaolin ores to feed the processing plant should ideally have high kaolinite abundance, be free in Fe-bearing mineralogy (to avoid influence in the colour of the product), and the kaolinite itself should be of high crystallinity (to ensure the correct abrasiveness after calcination). This work presents a case study from the kaolin deposits in the St. Austell Granite (South-West England), which are known for their high quality and world-class size. In this area, the kaolin is of primary-hydrothermal origin, with mineral associations that are related to the genetic history. The eventual depletion of the high-quality reserves is bringing now the attention to the lower grade zones, where the amount of impurities increases. As a consequence, it is critical to developing strategies that ensure the supply of high-quality ore to the processing plant. For this, it is necessary to acquire a thorough knowledge of the ore, including relative abundance of the minerals and their textural relationships. Hyperspectral images in the visible-near infrared (VNIR) and short-wave infrared (SWIR) ranges were collected from drill cores and run-off-mine (ROM) samples, obtained from one of the kaolin pits in the St. Austell area, where the kaolin quality is known to be lower than in the rest of the deposit. A series of mineral maps were generated to assess the distribution, texture and abundance of the Fe-bearing mineralogy and the other kaolin-associated minerals, as well as the variations in the crystallinity of kaolinite. The mineral maps enabled the identification of tourmaline, biotite and hematite as the Fe-bearing mineralogy. Tourmaline was found mainly in veins and sometimes as phenocrysts; biotite was rather scarce, which suggest the advanced alteration degree of the deposit; hematite was present as coating and concentrated along quartz veins. Most of the mineral associations were represented by kaolinite, halloysite, muscovite, illite and montmorillonite. The ground mass was mostly kaolinite, although transition zones from kaolinite to halloysite and kaolinite to mica and montmorillonite were detected. Regarding the kaolinite crystallinity, the pure kaolinite graded from high to very high crystallinity. For the mineral mixtures of kaolinite with montmorillonite or halloysite, the crystallinity could not be determined with confidence. These findings raise the possibility of using hyperspectral imaging as a tool for assisting selective mining, by identifying the areas in the deposit with the highest kaolin quality, thus reducing the amount of waste. In scenarios where selective mining is not possible, the spectral characterisation might provide robust mineralogical information about the content of the ore that can support the decision-making process in higher levels of the kaolin value chain.
FT-IR characterization of articulated ceramic bricks with wastes from ceramic industries
NASA Astrophysics Data System (ADS)
Nirmala, G.; Viruthagiri, G.
The 30 ceramic test samples with the kaolinitic clay and ceramic rejects (in the as-received state and sintered at temperatures 900-1200 °C) were investigated through spectral studies in order to elucidate the possibility of recycling the wastes from the government ceramic industry of Vriddhachalam, Tamilnadu state, South India. A detailed attribution of all the spectroscopic frequencies in the spectra recorded in the 4000-400 cm-1 region was attempted and their assignment to different minerals was accomplished. X-ray diffraction analysis was performed to demonstrate the reliability of IR attributions. The indication of well-ordered kaolinite is by the band at 1115 cm-1 in the raw samples which tends to shift towards 1095 cm-1 in all the fired samples. The peaks at 563 cm-1 and 795 cm-1 can be assigned to anorthite and dickite respectively. The presence of quartz and anorthite is confirmed both by XRD and FTIR. The microstructural observations were done through the SEM images which visualized the vitrification of the fired bricks at higher temperatures. The refractory properties of the samples found through the XRF analysis are also appreciable. The present work suggests that the incorporation of the rejects into the clay mixture will be a valid route for the ceramic industries to reduce the costs of the ceramic process.
FT-IR characterization of articulated ceramic bricks with wastes from ceramic industries.
Nirmala, G; Viruthagiri, G
2014-05-21
The 30 ceramic test samples with the kaolinitic clay and ceramic rejects (in the as-received state and sintered at temperatures 900-1200°C) were investigated through spectral studies in order to elucidate the possibility of recycling the wastes from the government ceramic industry of Vriddhachalam, Tamilnadu state, South India. A detailed attribution of all the spectroscopic frequencies in the spectra recorded in the 4000-400cm(-1) region was attempted and their assignment to different minerals was accomplished. X-ray diffraction analysis was performed to demonstrate the reliability of IR attributions. The indication of well-ordered kaolinite is by the band at 1115cm(-1) in the raw samples which tends to shift towards 1095cm(-1) in all the fired samples. The peaks at 563cm(-1) and 795cm(-1) can be assigned to anorthite and dickite respectively. The presence of quartz and anorthite is confirmed both by XRD and FTIR. The microstructural observations were done through the SEM images which visualized the vitrification of the fired bricks at higher temperatures. The refractory properties of the samples found through the XRF analysis are also appreciable. The present work suggests that the incorporation of the rejects into the clay mixture will be a valid route for the ceramic industries to reduce the costs of the ceramic process. Copyright © 2014 Elsevier B.V. All rights reserved.
Summary of Group Development and Testing for Single Shell Tank Closure at Hanford
DOE Office of Scientific and Technical Information (OSTI.GOV)
Harbour, John, R.
2005-04-28
This report is a summary of the bench-scale and large scale experimental studies performed by Savannah River National Laboratory for CH2M HILL to develop grout design mixes for possible use in producing fill materials as a part of Tank Closure of the Single-Shell Tanks at Hanford. The grout development data provided in this report demonstrates that these design mixes will produce fill materials that are ready for use in Hanford single shell tank closure. The purpose of this report is to assess the ability of the proposed grout specifications to meet the current requirements for successful single shell tank closuremore » which will include the contracting of services for construction and operation of a grout batch plant. The research and field experience gained by SRNL in the closure of Tanks 17F and 20F at the Savannah River Site was leveraged into the grout development efforts for Hanford. It is concluded that the three Hanford grout design mixes provide fill materials that meet the current requirements for successful placement. This conclusion is based on the completion of recommended testing using Hanford area materials by the operators of the grout batch plant. This report summarizes the regulatory drivers and the requirements for grout mixes as tank fill material. It is these requirements for both fresh and cured grout properties that drove the development of the grout formulations for the stabilization, structural and capping layers.« less
NASA Astrophysics Data System (ADS)
Li, Xiaoguang; Zhao, Ying; Xi, Beidou; Mao, Xuhui; Gong, Bin; Li, Rui; Peng, Xing; Liu, Hongliang
2016-05-01
In this study, natural clays were used as the support for nanoscale zero-valent iron (nZVI) to fulfill affordable and efficient decontamination materials. In comparison with the kaolinite (K) and montmorillonite (M) supported nZVI materials (K-nZVI and M-nZVI), Hangjin clay supported nZVI (HJ-nZVI) exhibited the best performance for nitrobenzene (NB) removal because of its favorable characteristics, such as higher specific surface area (SSA, 82.0 m2 g-1), larger pore volume (0.1198 cm3 g-1) and bigger average pore diameter (6.2 nm). The NB removal efficiency achieved by HJ-nZVI (93.2 ± 2.8%) was much higher than these achieved by HJ clay alone (38.2 ± 2.3%), nZVI alone (52.3 ± 2.5%) and by the combined use of nZVI and HJ clay (70.2 ± 1.3%). The superior performance of HJ-nZVI was associated with three aspects: the even distribution of nZVIs onto HJ clay, higher payload efficiency of nZVIs and the stronger adsorption capability of HJ clay support. Higher SSA, larger pore volume, favorable cation exchange capacity and structural negative charges all facilitated the payload of iron onto HJ clay. The adsorption process accelerated the reduction via increasing the local concentration of aqueous NB. The high efficiency of HJ-nZVI for decontamination warranted its promising prospect in remediation applications.
Characterization and inventory of PCDD/F emissions from the ceramic industry in China.
Lu, Mang; Wang, Guoxiang; Zhang, Zhongzhi; Su, Youming
2012-04-03
The ceramic industry is considered to be a potential source of dioxins (polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), considering the widespread distribution of dioxins in kaolinitic clays. Nevertheless, studies on the emission of dioxins from the ceramic industry are still very scarce. In this study, raw clays and stack gases from six typical ceramic plants in China were collected and analyzed to estimate the emission of dioxins from the ceramic industry. Dioxin profiles in raw clays were characterized by the domination of the congener octachlorodibenzo-p-dioxin (OCDD), and the contents of other congeners declined with the decreasing degree of chlorination. During the ceramic firing process, a considerable amount (16.5-25.1 wt % of the initial quantity in raw clays) of the dioxins was not destroyed and was released to the atmosphere. Dechlorination of OCDD generated a broad distribution within the PCDD congeners including a variety of non-2,3,7,8-substituted ones with the mass abundance of 0.4-3.6%. Based on the mean concentrations measured in this study, the inventory of PCDD/Fs from the manufacturing of ceramics on the Chinese scale was estimated to be 7.94 kg/year; the corresponding value on the I-TEQ basis is 133.6 g I-TEQ/year. This accounts for about 1.34% (I-TEQ basis) of the total emission of dioxins to the environment in China. The results suggest that the ceramic industry is a significant source of dioxins in the environment.
NASA Astrophysics Data System (ADS)
Do Campo, Margarita; Nieto, Fernando; del Papa, Cecilia; Hongn, Fernando
2014-07-01
In the northern part of the Calchaquí Valley (NW Argentina), Palaeogene Andean foreland sediments are represented by a 1400-metre-thick continental succession (QLC: Quebrada de Los Colorados Formation) consisting of claystones, siltstones, sandstones, and conglomerates representing sedimentation in fluvial-alluvial plains and alluvial fan settings. To understand the main syn- and postsedimentary variables controlling the clay mineral assemblages of this succession, we have studied the fine-grained clastic sediments by X-ray diffraction and electron microscopy, along with a detailed sedimentary facies analysis, for two representative sections. In the northern section, the whole succession was sampled and analysed by XRD, whereas in the second section, a control point 15 km to the south, only the basal levels were analysed. The XRD study revealed a strong contrast in clay mineral assemblages between these two sections as well as with sections in the central Calchaquí Valley studied previously. In the northernmost part of the study area, a complete evolution from smectite at the top to R3 illite/smectite mixed-layers plus authigenic kaolinite at the bottom, through R1-type mixed-layers in between, has been recognized, indicating the attainment of late diagenesis. In contrast, the clay mineral assemblages of equivalent foreland sediments cropping out only 15 km to the south contain abundant smectite and micas, subordinate kaolinite and chlorite, and no I/S mixed-layers to the bottom of the sequence. Early diagenetic conditions were also inferred in a previous study for equivalent sediments of the QLC Formation cropping out to the south, in the central Calchaquí Valley, as smectite occurs in basal strata. Burial depths of approximately 3000 m were estimated for the QLC Formation in the central and northern Calchaquí Valley; in addition, an intermediate to slightly low geothermal gradient can be considered likely for both areas as foreland basins are regarded as hypothermal basins. Consequently, the attainment of late diagenesis in the northernmost study area cannot be explained by significant differences in burial depth nor in geothermal gradient in relation to the section 15 km to the south nor with the central Calchaquí Valley. The formation of R3 mixed-layer I/S and authigenic kaolinite in the northern study area was most likely controlled by the circulation of hot, deep fluids along the reverse faults that bounded the Calchaquí valley. These faults were active during the Cenozoic, as evidenced by the syndepositional deformation features preserved in the studied sediments. Stress could also have been a driving force in burial diagenesis at the R3 mixed-layer I/S stage in these young continental sediments.
Finite element Analysis of Semi-Grouting Sleeve Connection Member Based on ABAQUS
NASA Astrophysics Data System (ADS)
Bao, Longsheng; Fan, Qianyu; Wang, Ling
2018-05-01
This paper use investigates the force transfer mechanism and failure form of semi-grouting sleeve members under axial load, analyze the weak points of structural bearing capacity and verify the reliability of the connection of steel bars through finite element analysis software. The results show that adding the axial load to semi-grouting sleeve forms a 45°oblique compression zone, which help to transfer stress between reinforcement, grouting material and sleeve. Because the maximum stress of sleeve doesn’t reach its tensile resistance and the deformation of the sleeve is located at the junction of the grouting and the threaded section when the stress value of steel bars at each end of the semi-grouting sleeve reach its ultimate tensile strength, we conclude that the semi-grouting sleeve members can meet the construction quality requirements and be used to connect the steel bars at the joints of the assembled structures. It is necessary to avoid breaking down, since the deformation section will accumulate large plastic deformation during the processing of the sleeve.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Koretsky, Carla
Hexavalent chromium is a highly toxic contaminant that has been introduced into aquifers and shallow sediments and soils via many anthropogenic activities. Hexavalent chromium contamination is a problem or potential problem in the shallow subsurface at several DOE sites, including Hanford, Idaho National Laboratory, Los Alamos National Laboratory and the Oak Ridge Reservation (DOE, 2008). To accurately quantify the fate and transport of hexavalent chromium at DOE and other contaminated sites, robust geochemical models, capable of correctly predicting changes in chromium chemical form resulting from chemical reactions occurring in subsurface environments are needed. One important chemical reaction that may greatlymore » impact the bioavailability and mobility of hexavalent chromium in the subsurface is chemical binding to the surfaces of particulates, termed adsorption or surface complexation. Quantitative thermodynamic surface complexation models have been derived that can correctly calculate hexavalent chromium adsorption on well-characterized materials over ranges in subsurface conditions, such pH and salinity. However, models have not yet been developed for hexavalent chromium adsorption on many important constituents of natural soils and sediments, such as clay minerals. Furthermore, most of the existing thermodynamic models have been developed for relatively simple, single solid systems and have rarely been tested for the complex mixtures of solids present in real sediments and soils. In this study, the adsorption of hexavalent chromium was measured as a function of pH (3-10), salinity (0.001 to 0.1 M NaNO3), and partial pressure of carbon dioxide(0-5%) on a suite of naturally-occurring solids including goethite (FeOOH), hydrous manganese oxide (MnOOH), hydrous ferric oxide (Fe(OH)3), γ-alumina (Al2O3), kaolinite (Al2Si2O5(OH)4), and montmorillonite (Na3(Al, Mg)2Si4O10(OH)2-nH2O). The results show that all of these materials can bind substantial quantities of hexavalent chromium, especially at low pH. Unexpectedly, experiments with the clay minerals kaolinite and montmorillonite suggest that hexavalent chromium may interact with these solids over much longer periods of time than expected. Furthermore, hexavalent chromium may irreversibly bind to these solids, perhaps because of oxidation-reduction reactions occurring on the surfaces of the clay minerals. More work should be done to investigate and quantify these chemical reactions. Experiments conducted with mixtures of goethite, hydrous manganese oxide, hydrous ferric oxide, γ-alumina, montmorillonite and kaolinite demonstrate that it is possible to correctly predict hexavalent chromium binding in the presence of multiple minerals using thermodynamic models derived for the simpler systems. Further, these models suggest that of the six solid considered in this study, goethite is typically the solid to which most of the hexavalent chromium will bind. Experiments completed with organic-rich and organic-poor natural sediments demonstrate that in organic-rich substrates, organic matter is likely to control uptake of the hexavalent chromium. The models derived and tested in this study for hexavalent chromium binding to γ-alumina, hydrous manganese oxide, goethite, hydrous ferric oxide and clay minerals can be used to better predict changes in hexavalent chromium bioavailability and mobility in contaminated sediments and soils.« less
Observations on Cretaceous abyssal hills in the northeast Pacific
Eittreim, S.L.; Piper, D.Z.; Chezar, H.; Jones, D.R.; Kaneps, A.
1984-01-01
An abyssal hills area of 50 ?? 60 km in the northeast Pacific was studied using bottom transponder navigation, closely spaced survey lines, and long-traverse oblique photography. The block-faulted north-south hills are bounded by scarps, commonly with 40?? slopes. On these steep scarps sedimentation is inhibited and pillow basalts often crop out. An ash layer of high acoustic reflectivity at about 7 m subbottom depth blankets the area. This ash occurs in multiple beds altered to phillipsite and is highly consolidated. A 24 m.y. age for the ash is based on ichthyolith dates from samples in the overlying sediments. Acoustically transparent Neogene sediments above the ash are thickest in trough bottoms and are absent or thin on steep slopes. These Neogene sediments are composed of pale-brown pelagic clays of illite, quartz, smectite, chlorite and kaolinite. Dark-brown pelagic clays, rich in smectite and amorphous iron oxides, underlie the Neogene surficial sediments. Manganese nodules cover the bottom in varying percentages. The nodules are most abundant near basement outcrops and where the subbottom ash layer is absent. ?? 1984.
NASA Technical Reports Server (NTRS)
Mackin, Steve; Munday, Tim; Hook, Simon
1987-01-01
Airborne Imaging Spectrometer-1 (AIS-1) data were flown over undifferentiated sequences of acid to intermediate volcanics and intrusives; meta-sediments; and a series of partially lateritized sedimentary rocks. The area exhibits a considerable spectral variability, after the suppression of striping effects. Log residual, and Internal Average Relative Reflectance (IARR) analytical techniques were used to enhance mineralogically related spectral features. Both methods produce similar results, but did not visually highlight mineral absorption features due to processing artifacts in areas of significant vegetation cover. The enhancement of mineral related absorption features was achieved using a hybrid processing approach based on the relative reflectance differences between vegetated and non-vegetated surfaces at 1.2 and 2.1 micron. The result is an image with little overall contrast, but which enhances the more subtle spectral features believed to be associated with clays and epidote. The AIS data was subject to interactive analysis using SPAM. Clear separation of clay and epidote related absorption features was apparent, and the identification of kaolinite was possible despite detrimental spectral effects.
[Analysis of XRD spectral characteristics of soil clay mineral in two typical cultivated soils].
Zhang, Zhi-Dan; Luo, Xiang-Li; Jiang, Hai-Chao; Li, Qiao; Shen, Cong-Ying; Liu, Hang; Zhou, Ya-Juan; Zhao, Lan-Po; Wang, Ji-Hong
2014-07-01
The present paper took black soil and chernozem, the typical cultivated soil in major grain producing area of Northeast, as the study object, and determinated the soil particle composition characteristics of two cultivated soils under the same climate and location. Then XRD was used to study the composition and difference of clay mineral in two kinds of soil and the evolutionary mechanism was explored. The results showed that the two kinds of soil particles were composed mainly of the sand, followed by clay and silt. When the particle accumulation rate reached 50%, the central particle size was in the 15-130 microm interval. Except for black soil profile of Shengli Xiang, the content of clay showed converse sequence to the central particle in two soils. Clay accumulated under upper layer (18.82%) in black soil profile while under caliche layer (17.41%) in chernozem profile. Clay content was the least in parent material horizon except in black profile of Quanyanling. Analysis of clay XRD atlas showed that the difference lied in not only the strength of diffraction peak, but also in the mineral composition. The main contents of black soil and chernozem were both 2 : 1 clay, the composition of black soil was smectite/illite mixed layer-illite-vermiculite and that of chernozem was S/I mixture-illite-montmorillonite, and both of them contained little kaolinite, chlorite, quartz and other primary mineral. This paper used XRD to determine the characteristics of clay minerals comprehensively, and analyzed two kinds of typical cultivated soil comparatively, and it was a new perspective of soil minerals study.
X-ray Diffraction and Rietveld Refinement in Deferrified Clays for Forensic Science.
Prandel, Luis V; Melo, Vander de F; Brinatti, André M; Saab, Sérgio da C; Salvador, Fábio A S
2018-01-01
Soil vestiges might provide information about a crime scene. The Rietveld method with X-ray diffraction data (RM-XRD) is a nondestructive technique that makes it possible to characterize minerals present in the soils. Soil clays from the metropolitan region of Curitiba (Brazil) were submitted to DCB treatment and analyzed using XRD with CuK α radiation in the step-scan mode (0.02° 2θ/5 s). The GSAS+EXPGUI software was used for RM refinement. The RM-XRD results, together with the principal component analysis (PCA) (52.6% total variance), showed the kaolinite predominance in most analyzed samples and the highest quartz contents in "site 1." Higher anatase, and gibbsite and muscovite contents influenced discrimination, mainly in "site 3" and "site 1," respectively. These results were enough to discriminate clays of four sites and two horizons using a reduced amount of sample showing that the technique can be applied to the investigation into soil vestiges. © 2017 American Academy of Forensic Sciences.
Halloysite Clay Nanotubes for Enzyme Immobilization.
Tully, Joshua; Yendluri, Raghuvara; Lvov, Yuri
2016-02-08
Halloysite clay is an aluminosilicate nanotube formed by rolling flat sheets of kaolinite clay. They have a 15 nm lumen, 50-70 nm external diameter, length of 0.5-1 μm, and different inside/outside chemistry. Due to these nanoscale properties, they are used for loading, storage, and controlled release of active chemical agents, including anticorrosions, biocides, and drugs. We studied the immobilization in halloysite of laccase, glucose oxidase, and lipase. Overall, negatively charged proteins taken above their isoelectric points were mostly loaded into the positively charged tube's lumen. Typical tube loading with proteins was 6-7 wt % from which one-third was released in 5-10 h and the other two-thirds remained, providing enhanced biocatalysis in nanoconfined conditions. Immobilized lipase showed enhanced stability at acidic pH, and the optimum pH shifted to more alkaline pH. Immobilized laccase was more stable with respect to time, and immobilized glucose oxidase showed retention of enzymatic activity up to 70 °C, whereas the native sample was inactive.
NASA Astrophysics Data System (ADS)
Gong, Fei; Di, Bangrang; Wei, Jianxin; Ding, Pinbo; Shuai, Da
2018-03-01
The presence of clay minerals can alter the elastic behaviour of reservoir rocks significantly as the type of clay minerals, their volume and distribution, and their orientation control the shale's intrinsic anisotropic behaviours. Clay minerals are the most abundant materials in shale, and it has been proven extremely difficult to measure the elastic properties of natural shale by means of a single variable (in this case, the type of clay minerals), due to the influences of multiple factors, including water, TOC content and complex mineral compositions. We used quartz, clay (kaolinite, illite and smectite), carbonate and kerogen extract as the primary materials to construct synthetic shale with different clay minerals. Ultrasonic experiments were conducted to investigate the anisotropy of velocity and mechanical properties in dry synthetic and natural shale as a function of confining pressure. Velocities in synthetic shale are sensitive to the type of clay minerals, possibly due to the different structures of the clay minerals. The velocities increase with confining pressure and show higher rate of velocity increase at low pressures, and P-wave velocity is usually more sensitive than S-wave velocity to confining pressure according to our results. Similarly, the dynamic Young's modulus and Poisson's ratio increase with applied pressure, and the results also reveal that E11 is always larger than E33 and ν31 is smaller than ν12. Velocity and mechanical anisotropy decrease with increasing stress, and are sensitive to stress and the type of clay minerals. However, the changes of mechanical anisotropy with applied stress are larger compared with the velocity anisotropy, indicating that mechanical properties are more sensitive to the change of rock properties.
NASA Astrophysics Data System (ADS)
Lopez, K. A.; Baron, D.; Guo, J.; Woolford, J. M.
2016-12-01
The early to middle Miocene Olcese Formation in the southern San Joaquin Valley of California consists of shallow marine shelf sands in its lower and upper parts, and non-marine, frequently pumiceous sands in its middle part, and varies in thickness up to 1800 ft. There is little known as to the origin, nature, quantity, and distribution of clay minerals throughout the formation. This study examined 95 sidewall core samples from three wells, as well as 388 cutting samples from four wells and 12 samples from 3 outcrops. Well samples were from depths between 1,800 and 4,000 ft. Qualitative and quantitative mineralogy including clay minerals of the sidewall samples and selected cutting samples was determined by powder X-ray diffraction (XRD). XRD analyses were supplemented by scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS) and petrographic microscopy of selected samples. The main minerals of bulk samples include composite clay, quartz, potassium feldspar/plagioclase, calcite, and clinoptilolite. Content of composite clay varies between 17% and 51%. The clay-size fraction is predominantly composed of smectite, illite, kaolinite and chlorite with smectite being the most abundant. Smectite and clinoptilolite may be the alteration products of deeper burial of volcanic materials. The formation permeability could be significantly lowered by these authigenic minerals.
Moon, Deok Hyun; Wazne, Mahmoud; Yoon, In-Ho; Grubb, Dennis G
2008-11-30
A stabilization/solidification (S/S) process for arsenic (As) contaminated soils was evaluated using cement kiln dust (CKD). Laboratory-prepared slurries, made of either kaolinite or montmorillonite, and field soils spiked with either As(3+) or As(5+) were prepared and treated with CKD ranging from 10 to 25 wt%. Sodium arsenite and sodium arsenate at 0.1 wt% were used to simulate arsenite (As(3+)) and arsenate (As(5+)) source contamination in soils, respectively. The effectiveness of treatment was evaluated at curing periods of 1- and 7-days based on the toxicity characteristic leaching procedure (TCLP). As-CKD and As-clay-CKD slurries were also spiked at 10 wt% to evaluate As immobilization mechanism using X-ray powder diffraction (XRPD) analyses. Overall, the TCLP results showed that only the As(5+) concentrations in kaolinite amended with 25 wt% CKD after 1 day of curing were less than the TCLP regulatory limit of 5mg/L. Moreover, at 7 days of curing, all As(3+) and As(5+) concentrations obtained from kaolinite soils were less than the TCLP criteria. However, none of the CKD-amended montmorillonite samples satisfied the TCLP-As criteria at 7 days. Only field soil samples amended with 20 wt% CKD complied with the TCLP criteria within 1 day of curing, where the source contamination was As(5+). XRPD and scanning electron microscopy (SEM)-energy dispersive X-ray spectroscopy (EDX) results showed that Ca-As-O and NaCaAsO(4).7.5H(2)O were the primary phases responsible for As(3+) and As(5+) immobilization in the soils, respectively.
Spatially resolved nanoscale observations of soil carbon multidecadal persistence
NASA Astrophysics Data System (ADS)
Lutfalla, S.; Chenu, C.; Bernard, S.; Le Guillou, C.; Barré, P.
2015-12-01
Assessing how mineral surfaces, especially at small scale, can protect soil organic carbon (SOC) from biodegradation is crucial. The question we address in this work is whether different mineral species lead to different organo-mineral interactions and stabilize different quantities of SOM and different types of SOC. Here we used the unique opportunity offered by long term bare fallows (BF) to study in situ C dynamics in several fine fractions of a silty loam soil. With no vegetation i.e. no external input of fresh C, the plant-free soil of the Versailles 42 Plots (INRA, France) has been progressively enriched in persistent SOC during the 80 years of BF. Contrasted mineral phases of the clay size fraction were isolated by size fractionation on samples from 5 different dates (0, 10, 22, 52, and 79 years after the beginning of the BF, four field replicates per date). Four fractions were studied: total clays (< 2 μm), and three sub fractions in the clay (fine clay: 0 - 0.05 μm, intermediate clay: 0.05 - 0.2 μm, and coarse clay: 0.2 - 2 μm). X-ray diffraction analyses showed contrasted mineralogies in the fine and intermediate clay (smectite and mixed layered illite/smectite) as opposed to the coarse clay (smectite, illite, kaolinite and mixed layered I/S). We performed CHN elemental analysis and synchrotron based spectroscopy and microscopy (NEXAFS bulk and STXM at the carbon K edge of 280 eV, CLS Saskatoon, Canada) to study the dynamics, the distribution and the chemical speciation of the SOC in these fractions. The quantity of C appears to be stabilized after 50 years of BF, even though the dynamics are different for the three clay fractions. Indeed, coarse and intermediate clays have the same final C content but coarse clays lose more C. Fine clay experiences the highest C losses and displays the highest final C content suggesting that fine clays contained more labile C and more persistent C. In all fractions, C:N ratios are really low (below 8) and are decreasing with time, evidencing the dominant presence of microbial SOC. STXM-NEXAFS data shows that, in the fine and intermediate clay fractions, during the first 50 years of BF all mineral particles are associated with SOC. On the contrary, in the coarse clays, SOC displays more diversity: the chemical signature is more diverse and mineral particles not associated with SOC appear more quickly.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Langton, C.; Stefanko, D.
2011-03-10
The objective of this report is to document laboratory testing of blended calcium aluminate - calcium hemihydrate grouts for P-Reactor vessel in-situ decommissioning. Blended calcium aluminate - calcium hemihydrate cement-based grout was identified as candidate material for filling (physically stabilizing) the 105-P Reactor vessel (RV) because it is less alkaline than portland cement-based grout which has a pH greater than 12.4. In addition, blended calcium aluminate - calcium hemihydrate cement compositions can be formulated such that the primary cementitious phase is a stable crystalline material. A less alkaline material (pH {<=} 10.5) was desired to address a potential materials compatibilitymore » issue caused by corrosion of aluminum metal in highly alkaline environments such as that encountered in portland cement grouts [Wiersma, 2009a and b, Wiersma, 2010, and Serrato and Langton, 2010]. Information concerning access points into the P-Reactor vessel and amount of aluminum metal in the vessel is provided elsewhere [Griffin, 2010, Stefanko, 2009 and Wiersma, 2009 and 2010, Bobbitt, 2010, respectively]. Radiolysis calculations are also provided in a separate document [Reyes-Jimenez, 2010].« less
Jinpeng, Zhang; Limin, Liu; Futao, Zhang; Junzhi, Cao
2018-04-04
With cement, bentonite, water glass, J85 accelerator, retarder and water as raw materials, a new composite grouting material used to seal groundwater inflow and reinforce wall rock in deep fractured rock mass was developed in this paper. Based on the reaction mechanism of raw material, the pumpable time, stone rate, initial setting time, plastic strength and unconfined compressive strength of multi-group proportion grouts were tested by orthogonal experiment. Then, the optimum proportion of composite grouting material was selected and applied to the grouting engineering for sealing groundwater inflow and reinforcing wall rock in mine shaft lining. The results show the mixing proportion of the maximum pumpable time, maximum stone rate and minimum initial setting time of grout are A K4 B K1 C K4 D K2 , A K3 B K1 C K1 D K4 and A K3 B K3 C K4 D K1 , respectively. The mixing proportion of the maximum plastic strength and unconfined compressive strength of grouts concretion bodies are A K1 B K1 C K1 D K3 and A K1 B K1 C K1 D K1 , respectively. Balanced the above 5 indicators overall and determined the optimum proportion of grouts: bentonite-cement ratio of 1.0, water-solid ratio of 3.5, accelerator content of 2.9% and retarder content of 1.45%. This new composite grouting material had good effect on the grouting engineering for sealing groundwater inflow and reinforcing wall rock in deep fractured rock mass.
The differences between soil grouting with cement slurry and cement-water glass slurry
NASA Astrophysics Data System (ADS)
Zhu, Mingting; Sui, Haitong; Yang, Honglu
2018-01-01
Cement slurry and cement-water glass slurry are the most widely applied for soil grouting reinforcement project. The viscosity change of cement slurry is negligible during grouting period and presumed to be time-independent while the viscosity of cement-water glass slurry increases with time quickly and is presumed to be time-dependent. Due to the significantly rheology differences between them, the grouting quality and the increasing characteristics of grouting parameters may be different, such as grouting pressure, grouting surrounding rock pressure, i.e., the change of surrounding rock pressure deduced by grouting pressure. Those are main factors for grouting design. In this paper, a large-scale 3D grouting simulation device was developed to simulate the surrounding curtain grouting for a tunnel. Two series of surrounding curtain grouting experiments under different geo-stress of 100 kPa, 150 kPa and 200 kPa were performed. The overload test on tunnel was performed to evaluate grouting effect of all surrounding curtain grouting experiments. In the present results, before 240 seconds, the grouting pressure increases slowly for both slurries; after 240 seconds the increase rate of grouting pressure for cement-water glass slurry increases quickly while that for cement slurry remains roughly constant. The increasing trend of grouting pressure for cement-water glass is similar to its viscosity. The setting time of cement-water glass slurry obtained from laboratory test is less than that in practical grouting where grout slurry solidifies in soil. The grouting effect of cement-water glass slurry is better than that of cement slurry and the grouting quality decreases with initial pressure.
Role of clay minerals in the transportation of iron
Carroll, D.
1958-01-01
The clay minerals have iron associated with them in several ways: 1. (1) as an essential constituent 2. (2) as a minor constituent within the crystal lattice where it is in isomorphous substitution and 3. (3) as iron oxide on the surface of the mineral platelets. Nontronite, "hydromica," some chlorites, vermiculite, glauconite and chamosite contain iron as an essential constituent. Kaolinite and halloysite have no site within the lattice for iron, but in certain environments iron oxide (goethite or hematite) is intimately associated as a coating on the micelles. Analyses of clay minerals show that the content of Fe2O3 varies: 29 per cent (nontronite), 7??3 per cent (griffithite), 4.5 per cent ("hydromica"), 5.5 per cent (chlorite), 4 per cent (vermiculite) and 18 per cent (glauconite). The FeO content is: 40 per cent (chamosite), 7.8 per cent (griffithite), 1-2 per cent ("hydromica"), 3 per cent (glauconite) and 2 per cent (chlorite). The iron associated with the clay minerals remains stable in the environment in which the minerals occur, but if either pH or Eh or both are changed the iron may be affected. Change of environment will cause: 1. (1) removal of iron by reduction of Fe3+ to Fe2+; 2. (2) ion-exchange reactions; 3. (3) instability of the crystal lattice. Experiments using bacterial activity to produce reducing conditions with kaolinite and halloysite coated with iron oxides and with nontronite in which ferric iron is in the octahedral position within the lattice showed that ferric oxide is removed at Eh +0??215 in fresh water and at Eh +0.098 in sea water. Hematite, goethite, and indefinite iron oxides were removed at different rates. Red ferric oxides were changed to black indefinite noncrystalline ferrous sulphide at Eh -0.020 but reverted to ferric oxide under oxidizing conditions. Nontronite turned bright green under reducing conditions and some of the ferrous iron remained within the lattice on a return to oxidizing conditions. Bacterial activity seems to be necessary for maintaining reducing conditions in the environments studied. ?? 1958.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Herich, Hanna; Tritscher, Torsten; Wiacek, Aldona
2009-11-01
Airborne mineral dust particles serve as cloud condensation nuclei (CCN), thereby influencing the formation and properties of warm clouds. It is therefore of particular interest how dust aerosols with different mineralogy behave when exposed to high relative humidity (RH) or supersaturation with respect to liquid water similar to atmospheric conditions. In this study the sub-saturated hygroscopic growth and the supersaturated cloud condensation nucleus activity of pure clays and real desert dust aerosols was determined using a hygroscopicity tandem differential mobility analyzer (HTDMA) and a cloud condensation nuclei counter (CCNC), respectively. Five different illite, montmorillonite and kaolinite clay samples as wellmore » as three desert dust samples (Saharan dust (SD), Chinese dust (CD) and Arizona test dust (ATD)) were used. Aerosols were generated both with a wet and a dry disperser and the water uptake was parameterized via the hygroscopicity parameter, κ. The hygroscopicity of dry generated dust aerosols was found to be negligible when compared to processed atmospheric aerosols, with CCNC derived κ values between 0.00 and 0.02. The latter value can be idealized as a particle consisting of 96.7% (by volume) insoluble material and ~3.3% ammonium sulfate. Pure clay aerosols were found to be generally less hygroscopic than real desert dust particles. All illite and montmorillonite samples had κ~0.003, kaolinites were least hygroscopic and had κ=0.001. SD (κ=0.023) was found to be the most hygroscopic dry-generated desert dust followed by CD (κ=0.007) and ATD (κ=0.003). Wet-generated dust showed an increased water uptake when compared to dry-generated samples. This is considered to be an artifact introduced by redistribution of soluble material between the particles while immersed in an aqueous medium during atomization, thus indicating that specification of the generation method is critically important when presenting such data. Any atmospheric processing of fresh mineral dust which leads to the addition of more than ~3% soluble material is expected to significantly enhance hygroscopicity and CCN activity.« less
NASA Astrophysics Data System (ADS)
Schindler, Michael; Legrand, Christine A.; Hochella, Michael F.
2015-03-01
Nano-scale processes on the solid-water interface of clay minerals control the mobility of metals in the environment. These processes can occur in confined pore spaces of clay buffers and barriers as well as in contaminated sediments and involve a combination of alteration, adsorption and nucleation processes of multiple species and phases. This study characterizes nano-scale processes on the interface between clay minerals and uranyl-bearing solution near neutral pH. Samples of clay minerals with a contact pH of ∼6.7 are collected from a U mill and mine tailings at Key Lake, Saskatchewan, Canada. The tailings material contains Cu-, As-, Co-, Mo-, Ni-, Se-bearing polymetallic phases and has been deposited with a surplus of Ca(OH)2 and Na2CO3 slaked lime. Small volumes of mill-process solutions containing sulfuric acid and U are occasionally discharged onto the surface of the tailings and are neutralized after discharge by reactions with the slaked lime. Transmission electron microscopy (TEM) in combination with the focused ion beam (FIB) technique and other analytical methods (SEM, XRD, XRF and ICP-OES) are used to characterize the chemical and mineralogical composition of phases within confined pore spaces of the clay minerals montmorillonite and kaolinite and in the surrounding tailings material. Alteration zones around the clay minerals are characterized by different generations of secondary silicates containing variable proportions of adsorbed uranyl- and arsenate-species and by the intergrowth of the silicates with the uranyl-minerals cuprosklodowskite, Cu[(UO2)2(SiO3OH)2](H2O)6 and metazeunerite, Cu[(UO2)(AsO4)2](H2O)8. The majority of alteration phases such as illite, illite-smectite, kaolinite and vermiculite have been most likely formed in the sedimentary basin of the U-ore deposit and contain low amounts of Fe (<5 at.%). Iron-enriched Al-silicates or illite-smectites (Fe >10 at.%) formed most likely in the limed tailings at high contact pH (∼10.5) and their structure is characterized by a low degree of long-range order. Adsorption of U and nucleation of metazeunerite and cuprosklodowskite are strongly controlled by the presence of the adsorbed oxy-anion species arsenate and silica on the Fe-enriched silicates. Heterogeneous nucleation of nano-crystals of the uranyl minerals occurs most likely on adsorption sites of binary uranyl-, arsenate- and silica-complexes as well as on ternary uranyl-arsenate or uranyl-silicate complexes. The uranyl minerals occur as aggregates of misoriented nano-size crystals and are the result of supersaturated solutions and a high number of nucleation sites that prevented the formation of larger crystals through Oswald ripening. The results of this study provide an understanding of interfacial nano-scale processes between uranyl species and altered clay buffers in a potential Nuclear Waste repository as similar alteration conditions of clays may occur in a multi-barrier system.
Adsorption of bacteriophages on clay minerals
Chattopadhyay, Sandip; Puls, Robert W.
1999-01-01
The ability to predict the fate of microorganisms in soil is dependent on an understanding of the process of their sorption on soil and subsurface materials. Presently, we have focused on studying the thermodynamics of sorption of bacteriophages (T-2, MS-2, and φX-174) on clays (hectorite, saponite, kaolinite, and clay fraction of samples collected from a landfill site). The thermodynamic study not only determines the feasibility of the process but also provides information on the relative magnitudes of the different forces under a particular set of conditions. The total free energy of interaction during sorption of bacteriophages on clays (ΔG) has been assumed to be the summation of ΔGH (ΔG due to hydrophobic interactions) and ΔGEL (ΔG due to electrostatic interactions). The magnitude of ΔGH was determined from the different interfacial tensions (γ) present in the system, while ΔGEL was calculated from ζ-potentials of the colloidal particles. Calculated results show that surface hydrophobicities of the selected sorbents and sorbates dictate sorption. Among the selected bacteriophages, maximum sorption was observed with T-2, while hectorite has the maximum sorption capacity. Experimental results obtained from the batch adsorption studies also corroborated those obtained from the theoretical study.
NASA Astrophysics Data System (ADS)
Mills, V. W.; Farmer, J. D.; Ruff, S. W.; Nunez, J.; Jahnke, L. L.
2011-12-01
The deposits of siliceous hydrothermal springs are known to capture and preserve a wide range of microbial fossil information. The recent discovery of hydrothermal silica at Home Plate, Columbia Hills, Mars has once again raised interest in the potential importance of ancient spring sinters as targets for future astrobiological mission to Mars. To create additional context information to support future in situ missions to Mars, we have documented systematic changes in the mineralogy and microtexture of modern siliceous hot spring deposits, observed along gradients in temperature, pH and flow velocity. Specific objectives are to: 1) identify chemical and physical factors that promote early diagenetic transformations of amorphous silica (opal-A), to progressively more ordered and crystalline phases (cristobalite, tridymite and quartz); 2) determine the composition and abundance of minor mineral phases, especially clays, in relationship to pH, temperature and paragenesis; and 3) to assess the usefulness of sinter mineralogy and microtexture in reconstructing the paleoenvironmental records preserved in ancient deposits. Study sites for acidic (pH 2-5) sinters included Nymph Creek, located in the Norris Geyser Basin of Yellowstone National Park (YNP). Active alkaline (pH 7-10) springs included Rabbit Creek, Steep Cone and Mound Spring located in the Lower Geyser Basin, YNP. Field measurements in active springs included pH, temperature and flow velocity, along with general microfacies assignments. To better constrain types and rates of silica diagenesis, the study also sampled older (Holocene-Pleistocene-aged) deposits. Laboratory analyses included X-ray powder diffraction (XRPD), thermal infrared spectroscopy (TIR) and thin section petrography for characterizing sinter microtextures and for placing mineral phases (identified by XRPD and TIR) into a time-ordered diagenetic framework. In analyzing the phyllosilicates present in sinters, we applied clay separation and glycolization methods, with XRPD. Results indicate that all of the acidic sinters we studied showed more extensive early diagenetic ordering of silica phases (opal-A to cristobalite and quartz) than the comparable microfacies of alkaline-neutral sinters. Clay analyses showed no evidence for smectitic (expansive) clays, but kaolin family clays (dickite, kaolinite and halloysite) were present in both acidic and alkaline sinters. The microfacies distribution observed for clays suggests: 1) dickite being more abundant in higher temperature (near-vent) microfacies, 2) kaolinite dominating mid-temperature outflow channels, slope and upper distal apron microfacies, and 3) halloysite being restricted to lower distal apron-marsh microfacies transitions. Future work will expand clay analyses to apply near-IR spectroscopy to a broader range of samples to assess the consistency with patterns suggested from XRPD.
Silica sol as grouting material: a physio-chemical analysis.
Sögaard, Christian; Funehag, Johan; Abbas, Zareen
2018-01-01
At present there is a pressing need to find an environmentally friendly grouting material for the construction of tunnels. Silica nanoparticles hold great potential of replacing the organic molecule based grouting materials currently used for this purpose. Chemically, silica nanoparticles are similar to natural silicates which are essential components of rocks and soil. Moreover, suspensions of silica nanoparticles of different sizes and desired reactivity are commercially available. However, the use of silica nanoparticles as grouting material is at an early stage of its technological development. There are some critical parameters such as long term stability and functionality of grouted silica that need to be investigated in detail before silica nanoparticles can be considered as a reliable grouting material. In this review article we present the state of the art regarding the chemical properties of silica nanoparticles commercially available, as well as experience gained from the use of silica as grouting material. We give a detailed description of the mechanisms underlying the gelling of silica by different salt solutions such as NaCl and KCl and how factors such as particle size, pH, and temperature affect the gelling and gel strength development. Our focus in this review is on linking the chemical properties of silica nanoparticles to the mechanical properties to better understand their functionality and stability as grouting material. Along the way we point out areas which need further research.
Mineralogical control of soil organic carbon persistence at the multidecadal time scale
NASA Astrophysics Data System (ADS)
Lutfalla, Suzanne; Barré, Pierre; Bernard, Sylvain; Le Guillou, Corentin; Chenu, Claire
2015-04-01
One of the current challenges in understanding the long term persistence of organic carbon in soils is to assess how mineral surfaces, especially at small scale, can stabilize soil organic carbon (SOC). The question we address in this work is whether different mineral species stabilize different types of SOC. Here we used the unique opportunity offered by long term bare fallows to study in situ C dynamics in several fine fractions of a silty loam soil. Indeed, with no vegetation i.e. no external input of fresh C, the plant-free soil of the Versailles 42 Plots (INRA, France) has been progressively enriched in persistent SOC during the 80 years of bare fallow. To separate mineral phases of the clay size fraction we performed a size fractionation on samples taken from 4 different plots at 5 different dates (0, 10, 22, 52, and 79 years after the beginning of the BF) and analyzed the SOC in the different fractions thus obtained. First, the clay fraction (< 2 µm) was isolated by wet sieving and centrifugation in water. Then, the clay fraction was further separated into 3 size fractions by centrifugation: fine clay (< 0.05 µm), intermediate clay (0.05 - 0.2 µm), and coarse clay (0.2 - 2 µm). X-ray diffraction was used to determine the mineralogy of the phases and we found that the coarse clay fraction on the one hand and fine and intermediate clay fractions on the other hand exhibited contrasted mineralogies. Fine and intermediate clay fractions contained almost exclusively smectite and mixed-layered illite/smectite minerals whereas coarse clays contained also discrete illite and kaolinite on top of smectite and illite/smectite. We carried out CHN elemental analysis to study the C and nitrogen dynamics with time in the different fractions. And synchrotron based spectroscopy and microscopy (NEXAFS bulk and STXM at the carbon K edge of 280 eV, CLS Saskatoon, Canada) was used to get information on the distribution and the chemical speciation of the SOC in fractions with contrasted mineralogies. Data analysis is still ongoing and full results will be presented at EGU. First results show that the dynamics and quality of the SOC differ in the different clay fractions. SOC decay was greater in coarse clays compared to intermediate clays, SOC in the coarse clay fraction displaying more diversity than in the other fractions. SOC persistence at the multidecadal timescale also seems to be mineral dependent: smectite being more efficient at protecting carbon compared to illite.
Effects of leachate on geotechnical characteristics of sandy clay soil
NASA Astrophysics Data System (ADS)
Harun, N. S.; Ali, Z. Rahman; Rahim, A. S.; Lihan, T.; Idris, R. M. W.
2013-11-01
Leachate is a hazardous liquid that poses negative impacts if leaks out into environments such as soil and ground water systems. The impact of leachate on the downgraded quality in terms of chemical characteristic is more concern rather than the physical or mechanical aspect. The effect of leachate on mechanical behaviour of contaminated soil is not well established and should be investigated. This paper presents the preliminary results of the effects of leachate on the Atterberg limit, compaction and shear strength of leachate-contaminated soil. The contaminated soil samples were prepared by mixing the leachate at ratiosbetween 0% and 20% leachate contents with soil samples. Base soil used was residual soil originated from granitic rock and classified as sandy clay soil (CS). Its specific gravity ranged between 2.5 and 2.64 with clay minerals of kaolinite, muscovite and quartz. The field strength of the studied soil ranged between 156 and 207 kN/m2. The effects of leachate on the Atterberg limit clearly indicated by the decrease in liquid and plastic limit values with the increase in the leachate content. Compaction tests on leachate-contaminated soil caused the dropped in maximum dry density, ρdry and increased in optimum moisture content, wopt when the amount of leachate was increased between 0% and 20%. The results suggested that leachate contamination capable to modify some geotechnical properties of the studied residual soils.
Mineralogy of a perudic Andosol in central Java, Indonesia
DOE Office of Scientific and Technical Information (OSTI.GOV)
Van Ranst, Eric; Utami, S. R.; Verdoodt, A.
2008-02-15
We studied the mineralogy of a perudic Andosol developed on the Dieng Tephra Sequence in central Java, Indonesia. The objective was to confirm the presence and determine the origin and stability of 2:1 and interlayered 2:1 phyllosilicates in well-drained Andosols. This was and still is a debated topic in the literature. Total elemental and selective dissolution, as well as microscopic and X-ray diffraction analyses, were performed on the soil samples collected from this site. These analyses confirmed that andic properties were present in the soil samples. The allophane content determined by selective dissolution was 3-4% in the A horizons, andmore » increased to 12-18% in the deeper subsoil horizons. In addition, the clay fraction contained dioctahedral smectite, hydroxy-Al-interlayered 2:1 minerals (HIS), Al-chlorite, kaolinite, pyrophyllite, mica, cristobalite and some gibbsite. The silt and sand fractions were rich in plagioclase and pyroxene. The 2:1 minerals (smectite and pyrophyllite), as well as chlorite and kaolinite were of hydrothermal origin and were incorporated in the tephra during volcanic eruption. Besides desilication during dissolution of unstable minerals, Al interlayering of 2:1 layer silicates was most likely the most prominent pedogenic process. Although hydroxy-Al polymeric interlayers would normally stabilize the 2:1 clay phases, the strong weakening, and even disappearance of the characteristic XRD peaks, indicated instability of these minerals in the upper A horizons due to the perudic and intensive leaching conditions.« less
DOE Office of Scientific and Technical Information (OSTI.GOV)
Loring, John S.; Schaef, Herbert T.; Turcu, Romulus VF
2012-04-25
The interaction of anhydrous supercritical CO2 (scCO2) with both kaolinite and ~1W (i.e. close to but less than one layer of hydration) calcium-saturated montmorillonite was investigated under conditions relevant to geologic carbon sequestration (50 °C and 90 bar). The CO2 molecular environment was probed in situ using a combination of three novel high-pressure techniques: X-ray diffraction, magic angle spinning nuclear magnetic resonance spectroscopy and attenuated total reflection infrared spectroscopy. We report the first direct evidence that the expansion of montmorillonite under scCO2 conditions is due to CO2 migration into the interlayer. Intercalated CO2 molecules are rotationally constrained and do notmore » appear to react with waters to form bicarbonate or carbonic acid. In contrast, CO2 does not intercalate into kaolinite. The findings show that predicting the seal integrity of caprock will have complex dependence on clay mineralogy and hydration state.« less
Nuzzo, Assunta; Piccolo, Alessandro
2013-05-13
The meso-tetra(2,6-dichloro-3-sulfonatophenyl)porphyrinate of manganese(III) chloride [Mn-(TDCPPS)Cl] biomimetic catalyst immobilized on spacer-functionalized kaolinite clay mineral was employed in the oxidative coupling reaction of a dissolved humic acid (HA) suprastructure with either chemical (H2O2) or UV-light oxidation. The changes in molecular size of humic matter subjected to catalyzed oxidative reaction were followed by high-performance size exclusion chromatography (HPSEC) with UV-vis and refractive index (RI) detectors in series, and by thermogravimetric (TGA) analysis. Both the enhanced molecular size shown by differences between HPSEC chromatograms of humic reaction mixtures at either pH 6 or 3.5 and the increase of thermogravimetric stability suggest that the heterogeneous biomimetic catalysis promoted the stabilization of humic conformations by new intermolecular covalent bonds during oxidative coupling. The similarity between chemical and light-induced oxidation results suggests potential multiple applications of the kaolinite-supported heterogeneous catalyst in controlling the reactivity of natural organic matter within biogeochemical cycles and environmental reactions.
[Mechanism of tritium persistence in porous media like clay minerals].
Wu, Dong-Jie; Wang, Jin-Sheng; Teng, Yan-Guo; Zhang, Ke-Ni
2011-03-01
To investigate the mechanisms of tritium persistence in clay minerals, three types of clay soils (montmorillonite, kaolinite and illite) and tritiated water were used in this study to conduct the tritium sorption tests and the other related tests. Firstly, the ingredients, metal elements and heat properties of clay minerals were studied with some instrumental analysis methods, such as ICP and TG. Secondly, with a specially designed fractionation and condensation experiment, the adsorbed water, the interlayer water and the structural water in the clay minerals separated from the tritium sorption tests were fractionated for investigating the tritium distributions in the different types of adsorptive waters. Thirdly, the location and configuration of tritium adsorbed into the structure of clay minerals were studied with infrared spectrometry (IR) tests. And finally, the forces and mechanisms for driving tritium into the clay minerals were analyzed on the basis of the isotope effect of tritium and the above tests. Following conclusions have been reached: (1) The main reason for tritium persistence in clay minerals is the entrance of tritium into the adsorbed water, the interlayer water and the structural water in clay minerals. The percentage of tritium distributed in these three types of adsorptive water are in the range of 13.65% - 38.71%, 0.32% - 5.96%, 1.28% - 4.37% of the total tritium used in the corresponding test, respectively. The percentages are different for different types of clay minerals. (2) Tritium adsorbed onto clay minerals are existed in the forms of the tritiated hydroxyl radical (OT) and the tritiated water molecule (HTO). Tritium mainly exists in tritiated water molecule for adsorbed water and interlayer water, and in tritiated hydroxyl radical for structural water. (3) The forces and effects driving tritium into the clay minerals may include molecular dispersion, electric charge sorption, isotope exchange and tritium isotope effect.
Kang, Chunxi; Wu, Pingxiao; Li, Yuewu; Ruan, Bo; Li, Liping; Tran, Lytuong; Zhu, Nengwu; Dang, Zhi
2015-11-01
Laboratory batch experiments were conducted to investigate the role of clay minerals, e.g., kaolinite and vermiculite, in microbial Cr(VI) reduction by Pseudomonas aeruginosa under growth condition in glucose-amended mediums as a method for treating Cr(VI)-contaminated subsurface environment such as soil. Our results indicated that glucose could acted as an essential electron donor, and clay minerals significantly enhanced microbial Cr(VI) reduction rates by improving the consumption rate of glucose and stimulating the growth and propagation of P. aeruginosa. Cr(VI) bioreduction by both free cells and clay minerals-amended cells followed the pseudo-first-order kinetic model, with the latter one fitting better. The mass balance analyses and X-ray photoelectron spectroscopy analysis found that Cr(VI) was reduced to Cr(III) and the adsorption of total chromium on clay minerals-bacteria complex was small, implying that Cr(VI) bioremoval was not mainly due to the adsorption of Cr(VI) onto cells or clay minerals or clay minerals-cells complex but mainly due to the Cr(VI) reduction capacity of P. aeruginosa under the experimental conditions studied (e.g., pH 7). Atomic force microscopy revealed that the addition of clay minerals (e.g. vermiculite) decreased the surface roughness of Cr(VI)-laden cells and changed the cell morphology and dimension. Fourier transform infrared spectroscopy revealed that organic matters such as aliphatic species and/or proteins played an important role in the combination of cells and clay minerals. Scanning electron microscopy confirmed the attachment of cells on the surface of clay minerals, indicating that clay minerals could provide a microenvironment to protect cells from Cr(VI) toxicity and serve as growth-supporting materials. These findings manifested the underlying influence of clay minerals on microbial reduction of Cr(VI) and gave an understanding of the interaction between pollutants, the environment and the biota.
Adsorption of bacterial plasmids in pure mineral mixtures
NASA Astrophysics Data System (ADS)
Zhang, L.; Cochran, J. P.; Seaman, J. C.; Parrott, B.
2017-12-01
Microorganisms play an important role in controlling the fate and transport of subsurface contaminants through the direct degradation of organic contaminants to the control of chemical redox conditions that impact the speciation and partitioning of inorganic contaminants. Genes that control these processes, including the relative tolerance associated with direct exposure to toxic contaminants, are found within the bacteria's chromosomal DNA and also within distinct, circular DNA elements called plasmids. Plasmids are mobile genetic elements that can be exchanged with other bacterial species through horizontal gene transfer (HGT). The frequency of HGT in soil is influenced by several factors, with the physicochemical characteristics of soil possibly being a primary factor. Thus, the objective for our research was to determine the movement and persistence of bacterial plasmids within soil. Our current study focuses on batch sorption experiments designed to evaluate the partitioning of bacterial plasmids in idealized mineral mixtures that represent the clay mineralogy of highly weathered soils of the Southeastern US. Specifically, we compared plasmid adsorption among pure goethite, kaolinite, and a mixture of goethite and kaolinite. We also determined the adsorption of plasmids on the above minerals over increasing pH (3 to 10). Our results show that adsorption decreased in the following order: goethite > kaolinite > mixture of goethite and kaolinite. We also found that plasmids adsorption was higher at lower pH levels, with pH 3 having the adsorption maximum. However, at pH 3, DNA denaturing may have occurred, leading to aggregation or precipitation of plasmids on the mineral surfaces. Our study was the first steps in determining the influence of soil properties on plasmid adsorption. Our future goals are to determine the adsorption in other pure minerals and in natural soils.
The physical model for research of behavior of grouting mixtures
NASA Astrophysics Data System (ADS)
Hajovsky, Radovan; Pies, Martin; Lossmann, Jaroslav
2016-06-01
The paper deals with description of physical model designed for verification of behavior of grouting mixtures when applied below underground water level. Described physical model has been set up to determine propagation of grouting mixture in a given environment. Extension of grouting in this environment is based on measurement of humidity and temperature with the use of combined sensors located within preinstalled special measurement probes around grouting needle. Humidity was measured by combined capacity sensor DTH-1010, temperature was gathered by a NTC thermistor. Humidity sensors measured time when grouting mixture reached sensor location point. NTC thermistors measured temperature changes in time starting from initial of injection. This helped to develop 3D map showing the distribution of grouting mixture through the environment. Accomplishment of this particular measurement was carried out by a designed primary measurement module capable of connecting 4 humidity and temperature sensors. This module also takes care of converting these physical signals into unified analogue signals consequently brought to the input terminals of analogue input of programmable automation controller (PAC) WinPAC-8441. This controller ensures the measurement itself, archiving and visualization of all data. Detail description of a complex measurement system and evaluation in form of 3D animations and graphs is supposed to be in a full paper.
A new design concept of fully grouted rock bolts in underground construction
NASA Astrophysics Data System (ADS)
Phich Nguyen, Quang; Nguyen, Van Manh; Tuong Nguyen, Ke
2018-04-01
The main problem after excavating an underground excavation is to maintain the stability of the excavation for a certain period of time. Failure in meeting this demand is a threat to safety of men and equipment. Support and reinforcement are different instruments with different mechanisms. Among the common support systems in tunnelling and mining, rock bolts have been widely used to reinforce rock mass and also to reduce geological hazards. Furthermore rock bolts can be applied under varying different geological conditions with cost-effectiveness. Although different methods are developed for grouted rock bolts design until now, the interaction mechanism of the rock bolts and rock mass is still very complicated issue. The paper addresses an analytical model for the analysis and design of fully grouted rock bolts based on the reinforcement principle. According to this concept the jointed rock mass reinforced by grouted rock bolts is considered as composite material which includes rock mass, the grout material and the bolt shank. The mechanical properties of this composite material depend on the ratio of the components. The closed-form solution was developed based on the assumption that the rock mass arround a circular tunnel remained elastic after installing fully grouted rock bolts. The main parameters of the rock-bolt system (the diameter and length of bolt shank, the space between the bolts) are then easily estimated from the obtained solution.
Experimental Characterization of Stress- and Strain-Dependent Stiffness in Grouted Rock Masses.
Kim, Ji-Won; Chong, Song-Hun; Cho, Gye-Chun
2018-03-29
Grouting of fractured rock mass prior to excavation results in grout-filled discontinuities that govern the deformation characteristics of a site. The influence of joint characteristics on the properties of grouted rocks is important in assessing the effects of grouting on jointed rock mass. However, grouting remains a predominantly empirical practice and the effects of grouting on rock joint behavior and material properties have yet to be accurately assessed. Granular materials, including jointed rocks, typically display nonlinear strain-dependent responses that can be characterized by the shear modulus degradation curve. In this study, the effects of grouting on the strain-dependent shear stiffness of jointed rock mass were investigated at the small-strain (below 10 -5 ) and mid-strain (10 -5 to 10 -3 ) ranges using the quasi-static resonant column test and rock mass dynamic test devices. The effects of curing time, axial stress, initial joint roughness, and grouted joint thickness were examined. The results show that (1) grouting of rock joints leads to decreased stress sensitivity and increased small-strain shear stiffness for all tested samples; (2) the grouted rock samples display similar modulus degradation characteristics as the applied grout material; (3) the initial joint roughness determines the stress-dependent behaviors and general stiffness range of the jointed and grouted rocks, but the strain-dependent behaviors are dependent on the properties of the grout material; (4) increased grouted joint thickness results in larger contribution of the grout properties in the overall grouted rock mass.
Experimental Characterization of Stress- and Strain-Dependent Stiffness in Grouted Rock Masses
Cho, Gye-Chun
2018-01-01
Grouting of fractured rock mass prior to excavation results in grout-filled discontinuities that govern the deformation characteristics of a site. The influence of joint characteristics on the properties of grouted rocks is important in assessing the effects of grouting on jointed rock mass. However, grouting remains a predominantly empirical practice and the effects of grouting on rock joint behavior and material properties have yet to be accurately assessed. Granular materials, including jointed rocks, typically display nonlinear strain-dependent responses that can be characterized by the shear modulus degradation curve. In this study, the effects of grouting on the strain-dependent shear stiffness of jointed rock mass were investigated at the small-strain (below 10−5) and mid-strain (10−5 to 10−3) ranges using the quasi-static resonant column test and rock mass dynamic test devices. The effects of curing time, axial stress, initial joint roughness, and grouted joint thickness were examined. The results show that (1) grouting of rock joints leads to decreased stress sensitivity and increased small-strain shear stiffness for all tested samples; (2) the grouted rock samples display similar modulus degradation characteristics as the applied grout material; (3) the initial joint roughness determines the stress-dependent behaviors and general stiffness range of the jointed and grouted rocks, but the strain-dependent behaviors are dependent on the properties of the grout material; (4) increased grouted joint thickness results in larger contribution of the grout properties in the overall grouted rock mass. PMID:29596371
NASA Astrophysics Data System (ADS)
Ndjigui, Paul-Désiré; Onana, Vincent Laurent; Sababa, Elisé; Bayiga, Elie Constantin
2018-07-01
The Lokoundje alluvial clay deposits are located at the left floodplain of the Lokoundje River, towards the estuary in the Kribi region. The mineralogical and geochemical features of the Lokoundje River fine-grained sediments have been reported using XRD, XRF, ICP-MS, and IR instruments in order to understand their provenance and depositional history. The Lokoundje watershed covers a surface area of about 5381 km2. The basement of this watershed is made up of gneisses, amphibolites, migmatites, charnockites, and pyroxenites from the Nyong and Ntem units, in the NW border of the Congo craton. The alluvial materials are about 100 cm thick and cover a total area of 1.4 km2. They are mainly plastic clays with silty-clayey texture and four colors (yellow, red yellow, white, and light grey). The mineral assemblage is composed of kaolinite, quartz, illite, gibbsite, goethite, rutile, and interstratified illite-vermiculite. The infra-red data associated with those of XRD portray the disordering of kaolinite. These materials are mostly constituted by SiO2 (44.33-69.19 wt%, av. = 51.17 wt% with n = 18) and Al2O3 (20.69-30.26 wt%, av. = 26.07 wt%) with very low Fe2O3 contents (1-7.71 wt%, av. = 3.35 wt%). The SiO2/Al2O3 ratio range between 1.46 and 4.1 (av. = 2.06). The alkali contents (Na2O + K2O) are below 5 wt%. ICV, CIA, PIA, and SiO2/Al2O3 portray high degree of chemical weathering in the source area as well as the maturity of sediments. The trace element behavior is quite different probably due to the mixed source rocks; Ba, Sr, Zn have high contents while several elements such as Th and U show low contents. The REE contents are also variable; their concentrations vary between 92 and 1065 ppm (av. = 307 ppm). The mineral assemblage associated with the geochemical data reveal that REE are mainly housed in clay minerals. The behavior of REE is also marked by the abundance of LREE (LREE/HREE = 19.69-34.62). The REE chondrite-normalized spectra confirm the LREE-abundance and exhibit negative Eu anomalies. The PAAS-normalized patterns reveal slight positive Eu anomalies and negative Ce anomalies. The (La/Yb)N values (3.30-8.43, av. = 5.71) display low degree of REE-fractionation in the Lokoundje watershed. The morphological, mineralogical, and geochemical features reveal that the fine-grained sediments derive from the intense weathering of mixed source. The disordering of kaolinite confirms that sediments were sorted during a long transportation before their deposition under oxic conditions (U/Th < 1.25; V/Cr < 2) in the floodplains near the Atlantic coast.
Holmstrand, Henry; Gadomski, Damien; Mandalakis, Manolis; Tysklind, Mats; Irvine, Robert; Andersson, Per; Gustafsson, Orjan
2006-06-15
Polychlorinated dibenzo-p-dioxins (PCDDs) of high concentrations in a ball clay deposit from the Mississippi Embayment were found to be consistent with a natural abiotic and non-pyrogenic origin by investigation with bulk radiocarbon analysis, compound-specific chlorine isotope analysis (CSIA-delta37Cl) of octachlorodibenzo-p-dioxin (OCDD), and black carbon (BC) analysis. The conventional radiocarbon date of total organic carbon from a depth of approximately 10 m in three parallel cores ranged from 14 700 years to >48 000 years, indicating that the strata with elevated levels of PCDDs have remained isolated from recent anthropogenic input in these >40 Ma old clay sediments. The CSIA-delta37Cl of OCDD yielded a delta37Cl of -0.2 per thousandth, which is significantly higher than the postulated range for biotic chlorination by chloroperoxidase enzymes, -11 to -10 per thousandth, and falls within the known range for abiotic organochlorines, -6 to +3 per thousandth. The absence of correlations between concentrations of PCDDs and corresponding pyrogenic black carbon (BC), together with estimations of BC sorptive loadings and the absence of polychlorinated dibenzofurans (PCDFs), suggest that vegetation fires did not form these ball-clay PCDDs. Results from this study indicate that the high levels of the toxic and carcinogenic PCDDs found in kaolinite-bearing clays may result from natural abiotic formation via in situ surface-promoted reactions on the clay mineral, including a so-far unknown organic precursor, rather than being the result of anthropogenic contamination.
Zhang, Zhi-dan; Li, Qiao; Luo, Xiang-li; Jiang, Hai-chao; Zheng, Qing-fu; Zhao, Lan-po; Wang, Ji-hong
2014-08-01
The present paper took the typical saline-alkali soil in Jilin province as study object, and determinated the soil clay mineral composition characteristics of soil in paddy field and dry land. Then XRD spectrum was used to analyze the evolutionary mechanism of clay mineral in the two kinds of soil. The results showed that the physical and chemical properties of soil in paddy field were better than those in dry land, and paddy field would promote the weathering of mineral particles in saline-alkali soil and enhance the silt content. Paddy field soil showed a strong potassium-removal process, with a higher degree of clay mineral hydration and lower degree of illite crystallinity. Analysis of XRD spectrum showed that the clay mineral composition was similar in two kinds of soil, while the intensity and position of diffraction peak showed difference. The evolution process of clay mineral in dry land was S/I mixture-->vermiculite, while in paddy field it was S/I mixture-->vermiculite-->kaolinite. One kind of hydroxylated 'chlorite' mineral would appear in saline-alkali soil in long-term cultivated paddy field. Taking into account that the physical and chemical properties of soil in paddy field were better then those in dry land, we could know that paddy field could help much improve soil structure, cultivate high-fertility soil and improve saline-alkali soil. This paper used XRD spectrum to determine the characteristics of clay minerals comprehensively, and analyzed two'kinds of land use comparatively, and was a new perspective of soil minerals study.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Ren, Li-Te; College of Materials Science and Engineering, Nanjing Tech University, Nanjing 210009; Li, Xiao-Pei
2015-12-15
The proton-conducting materials have potential application in devices such as fuel cells. In this study, a mineral kaolinite-based proton conducting material, kaolinite-4-amidinopyridinium hydrochloride (K-4-APy–HCl), was synthesized by the intercalated compound kaolinite-4-amidinopyridine (K-4-APy) adsorbing volatilizing HCl. The thermogravimetric analysis (TG), powder X-ray diffraction (PXRD) and IR spectrum confirmed the HCl successfully inserting into the interlayer space of kaolinite and the 4-aminopyridine being protonated. The intercalation efficiency is estimated to be ca. 85.6%. With respect to K-4-APy, the interlayer space expends by 1.53 Å. The thermal decomposition mechanism was studied by PXRD and TG techniques. The K-4-APy–HCl shows proton conductivity with σ=3.379×10{supmore » −8} S cm{sup −1} at 373 K and E{sub a}=1.159 eV in the anhydrous condition, which are comparable to MOFs-based proton conducting materials. - Graphical abstract: The intercalated hybrid of mineral kaolinite with 4-amidinopyridinium hydrochloride is prepared to use as proton conducting material. - Highlights: • A new strategy is proposed for preparation of kaolinite-based proton conductor. • Intercalatied hybrid was prepared by sequentially inserting 4-amidinopyridine and adsorbing HCl. • The proton conductivity of intercalated hybrid is comparable to MOFs-based proton-conductors.« less
Jiang, Tianyong; Song, Gangbing
2017-01-01
With the development of the post-tensioning technique, prestressed concrete structures have been widely used in civil engineering. To ensure the long-term effectiveness of the prestressed tendon, the grouting quality of the tendon duct is one of the important factors. However, it is still a challenge to monitor the grouting quality of post-tensioning tendon ducts, due to the invisibility of the grouting. The authors’ previous work proposed a real-time method that employed a stress wave-based active sensing approach with piezoceramic transducers to monitor the grouting compactness of a Post-Tensioning Tendon Duct (PTTD). To further understand the piezoceramic induced stress wave propagation in the PTTD with different grouting levels, this paper develops a two-dimensional finite element model for monitoring the grouting compactness of the tendon duct with a piezoceramic transducer. A smart aggregate (SA) developed to utilize one Lead Zirconate Titanate (PZT) transducer with marble protection is installed in the center location of the tendon duct as an actuator. Two PZT patches are bonded on the bottom and top surface of the tendon duct as the sensors. The analysis results show that the finite element analysis results are in good agreement with the experimental results, which demonstrates that the finite element analysis is feasible and reliable. For the top half of the specimen, not much stress wave could be detected before the full grouting level, except for negligible signals that may propagate through the walls of the tendon duct. When the tendon duct grouting is at 100%, the stress wave propagates to the top of the specimen, and the displacements are symmetric in both left-right and top-bottom directions before the stress waves reach the boundary. The proposed two-dimensional finite element model has the potential to be implemented to simulate the stress wave propagation principle for monitoring grouting compaction of the post-tensioning tendon duct. PMID:28961173
Jiang, Tianyong; Zheng, Junbo; Huo, Linsheng; Song, Gangbing
2017-09-29
With the development of the post-tensioning technique, prestressed concrete structures have been widely used in civil engineering. To ensure the long-term effectiveness of the prestressed tendon, the grouting quality of the tendon duct is one of the important factors. However, it is still a challenge to monitor the grouting quality of post-tensioning tendon ducts, due to the invisibility of the grouting. The authors' previous work proposed a real-time method that employed a stress wave-based active sensing approach with piezoceramic transducers to monitor the grouting compactness of a Post-Tensioning Tendon Duct (PTTD). To further understand the piezoceramic induced stress wave propagation in the PTTD with different grouting levels, this paper develops a two-dimensional finite element model for monitoring the grouting compactness of the tendon duct with a piezoceramic transducer. A smart aggregate (SA) developed to utilize one Lead Zirconate Titanate (PZT) transducer with marble protection is installed in the center location of the tendon duct as an actuator. Two PZT patches are bonded on the bottom and top surface of the tendon duct as the sensors. The analysis results show that the finite element analysis results are in good agreement with the experimental results, which demonstrates that the finite element analysis is feasible and reliable. For the top half of the specimen, not much stress wave could be detected before the full grouting level, except for negligible signals that may propagate through the walls of the tendon duct. When the tendon duct grouting is at 100%, the stress wave propagates to the top of the specimen, and the displacements are symmetric in both left-right and top-bottom directions before the stress waves reach the boundary. The proposed two-dimensional finite element model has the potential to be implemented to simulate the stress wave propagation principle for monitoring grouting compaction of the post-tensioning tendon duct.
NASA Astrophysics Data System (ADS)
Lintz, L.; Werts, S. P.
2014-12-01
The Ninety-Six National Historic Site is located in Greenwood County, SC. Recent geologic mapping of this area has revealed differences in soil properties over short distances within the park. We studied the chemistry of the clay minerals found within the soils to see if there was a correlation between the amounts of soil organic carbon contained in the soil and particle size in individual soil horizons. Three different vegetation areas, including an old field, a deciduous forest, and a pine forest were selected to see what influence vegetation type had on the clay chemistry and carbon levels as well. Four samples containing the O, A, and B horizons were taken from each location and we studied the carbon and nitrogen content using an elemental analyzer, particle size using a Laser Diffraction Particle Size Analyzer, and clay mineralogy with powder X-ray diffraction of each soil sample. Samples from the old field and pine forest gave an overall negative correlation between carbon content and clay percentage, which is against the normal trend for Southern Piedmont Ultisols. The deciduous forest samples gave no correlation at all between its carbon content and clay percentage. Together, all three locations show the same negative relationship, while once separated into vegetation type and A and B horizons it shows even more abnormal relationships of negative while several show no correlation (R2= 0.007403- 0.56268). Using powder XRD, we ran clay samples from each A and B horizon for the clay mineralogy. All three vegetation areas had the same results of containing quartz, kaolinite, and Fe oxides, therefore, clay chemistry is not a reason behind the abnormal trend of a negative correlation between average carbon content and clay percentage. Considering that all three locations have the same climate, topography, and parent material of metagranite, it could be reasonable to assume these results are a factor of environmental and biological influences rather than clay type.
Potential bioavailability of mercury in humus-coated clay minerals.
Zhu, Daiwen; Zhong, Huan
2015-10-01
It is well-known that both clay and organic matter in soils play a key role in mercury biogeochemistry, while their combined effect is less studied. In this study, kaolinite, vermiculite, and montmorillonite were coated or not with humus, and spiked with inorganic mercury (IHg) or methylmercury (MeHg). The potential bioavailability of mercury to plants or deposit-feeders was assessed by CaCl2 or bovine serum albumin (BSA) extraction. For uncoated clay, IHg or MeHg extraction was generally lower in montmorillonite, due to its greater number of functional groups. Humus coating increased partitioning of IHg (0.5%-13.7%) and MeHg (0.8%-52.9%) in clay, because clay-sorbed humus provided more strong binding sites for mercury. Furthermore, humus coating led to a decrease in IHg (3.0%-59.8% for CaCl2 and 2.1%-5.0% for BSA) and MeHg (8.9%-74.6% for CaCl2 and 0.5%-8.2% for BSA) extraction, due to strong binding between mercury and clay-sorbed humus. Among various humus-coated clay particles, mercury extraction by CaCl2 (mainly through cation exchange) was lowest in humus-coated vermiculite, explained by the strong binding between humus and vermiculite. The inhibitory effect of humus on mercury bioavailability was also evidenced by the negative relationship between mercury extraction by CaCl2 and mercury in the organo-complexed fraction. In contrast, extraction of mercury by BSA (principally through complexation) was lowest in humus-coated montmorillonite. This was because BSA itself could be extensively sorbed onto montmorillonite. Results suggested that humus-coated clay could substantially decrease the potential bioavailability of mercury in soils, which should be considered when assessing risk in mercury-contaminated soils. Copyright © 2015. Published by Elsevier B.V.
Analysis on pile testing results of post-grouting bored pile
NASA Astrophysics Data System (ADS)
Zheng, A. R.
2017-04-01
Based on static load test results, the bearing capacity of bored piles with pile-toe and pile-shaft post-grouting has been analyzed. The analysis reveals that: with post-grouting, the interface between pile and surrounding soil are strengthened and the relative sliding displacement in between is reduced; end resistance of pile is enhanced and can be mobilized at earlier stage with smaller sliding displacement. As a result, the performance of bored pile is improved with increased bearing capacity and reduced settlement.
Halloysite nanotubule clay for efficient water purification.
Zhao, Yafei; Abdullayev, Elshad; Vasiliev, Alexandre; Lvov, Yuri
2013-09-15
Halloysite clay has chemical structure similar to kaolinite but it is rolled in tubes with diameter of 50 nm and length of ca. 1000 nm. Halloysite exhibits higher adsorption capacity for both cationic and anionic dyes because it has negative SiO2 outermost and positive Al2O3 inner lumen surface; therefore, these clay nanotubes have efficient bivalent adsorbancy. An adsorption study using cationic Rhodamine 6G and anionic Chrome azurol S has shown approximately two times better dye removal for halloysite as compared to kaolin. Halloysite filters have been effectively regenerated up to 50 times by burning the adsorbed dyes. Overall removal efficiency of anionic Chrome azurol S exceeded 99.9% for 5th regeneration cycle of halloysite. Chrome azurol S adsorption capacity decreases with the increase of ionic strength, temperature and pH. For cationic Rhodamine 6G, higher ionic strength, temperature and initial solution concentration were favorable to enhanced adsorption with optimal pH 8. The equilibrium adsorption data were described by Langmuir and Freundlich isotherms. Copyright © 2013 Elsevier Inc. All rights reserved.
Alagha, Lana; Wang, Shengqun; Yan, Lujie; Xu, Zhenghe; Masliyah, Jacob
2013-03-26
Quartz crystal microbalance with dissipation (QCM-D) was applied to investigate the adsorption characteristics of polyacrylamide-based polymers (PAMs) on anisotropic basal planes of kaolinite. Kaolinite basal planes were differentiated by depositing kaolinite nanoparticles (KNPs) on silica and alumina sensors in solutions of controlled pH values. Adsorption of an in-house synthesized organic-inorganic Al(OH)3-PAM (Al-PAM) as an example of cationic hybrid PAM and a commercially available partially hydrolyzed polyacrylamide (MF1011) as an example of anionic PAM was studied. Cationic Al-PAM was found to adsorb irreversibly and preferentially on tetrahedral silica basal planes of kaolinite. In contrast, anionic MF1011 adsorbed strongly on aluminum-hydroxy basal planes, while its adsorption on tetrahedral silica basal planes was weak and reversible. Adsorption study revealed that both electrostatic attraction and hydrogen-bonding mechanisms contribute to adsorption of PAMs on kaolinite. The adsorbed Al-PAM layer was able to release trapped water overtime and became more compact, while MF1011 film became more dissipative as backbones stretched out from kaolinite surface with minimal overlapping. Experimental results obtained from this study provide clear insights into the phenomenon that governs flocculation-based solid-liquid separation processes using multicomponent flocculants of anionic and cationic nature.
Antenna grout replacement system
NASA Technical Reports Server (NTRS)
Mcclung, C. E. (Inventor)
1983-01-01
An epoxy grout suitable for use in mounting and positioning bearing runner plates used in hydrostatic bearing assemblies for rotatably mounting large radio telescope structures to stationary support pedestals is described. The epoxy grout may be used in original mountings or may be used as part of a replacement system for repairing cavities in existing grout resulting from grout deterioration. The epoxy grout has a relatively short work life and cure time even in the presence of hydraulic oil. The epoxy grout cures without shrinking or sagging to form a grout which is sufficiently strong and durable to provide a grout especially well suited for use under the high pressure loading and close tolerance requirements of large hydrostatic bearing assemblies.
NASA Astrophysics Data System (ADS)
Liu, Yong Jun; Li, Chao; Zhou, When Jun
2018-06-01
This paper presents some numerical simulation results of tensile properties of reinforcing bars spliced by grout-filled coupling sleeves under fire conditions to identify the effect of load ratio on fire resistance time of spliced reinforcing bars, which provide a useful base for predicting structural behaviors of pre-cast reinforced concrete buildings in fires. A spliced rebar system investigated in this paper consists of two equal-diameter steel reinforcing bars with 25mm diameter and a straight coupling sleeve with 50mm outer and 45mm inner diameters. As a result, the thickness of grout between steel bars and sleeves are 20mm. Firstly, the temperature distributions in steel bars connected by grout- filled coupling sleeves exposed to ISO 834 standard fire were calculated utilizing finite element analysis software ANSYS. Secondly, the stress changes in heated steel bars connected by grout-filled coupling sleeves under different constant tensile loads were calculated step by step until the rebar system failed due to fire. Thus, the fire resistant time of rebar spliced by grout-filled coupling sleeves under different axial tensile loads can be determined, further, the relationship between fire resistance time and axial tensile loads ratio can could be obtained. Finally, the fire resistant times versus axial tensile load ratios curve of grout-filled splice sleeve rebars exposed to ISO 834 standard fire is presented.
NASA Astrophysics Data System (ADS)
Bello Yamusa, Yamusa; Yunus, Nor Zurairahetty Mohd; Ahmad, Kamarudin; Rahman, Norhan Abd; Sa'ari, Radzuan
2018-03-01
Laterite soil was investigated to find out the effects of fines content and to identify the micro-structural and molecular characteristics to evaluate its potentiality as a compacted soil landfill liner material. Tests were carried out on natural soil and reconstituted soil by dry weight of soil samples to determine the physical and engineering properties of the soil. All tests were carried out on the samples by adopting the British Standard 1377:1990. The possible mechanisms that contributed to the clay mineralogy were analyzed using spectroscopic and microscopic techniques such as field emission scanning electron microscopy (FESEM), energy-dispersive X-ray (EDX) and X-ray diffractometry (XRD). The laterite soil was found to contain kaolinite as the major clay minerals. A minimum of 50% fines content of laterite soil met the required result for hydraulic barriers in waste containment facilities.
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.
Enrofloxacin uptake and retention on different types of clays
NASA Astrophysics Data System (ADS)
Wan, Miao; Li, Zhaohiu; Hong, Hanlie; Wu, Qingfeng
2013-11-01
The adsorption and retention of enrofloxacin (EN) on different types of clays was studied in batch tests under different pH, contact time, and initial concentration conditions. XRD and FTIR analyses were utilized to characterize EN adsorption and to elucidate mechanisms of EN adsorption. The EN adsorption equilibrium followed the Langmuir isotherm and reached capacities of 667, 228 and 20 mmol/kg at pH 4-5 on the montmorillonite (SWy-2), illite (IMt-2), and kaolinite (KGa-1b), respectively. The pseudo-second-order model fitted the EN sorption kinetics well. Although EN had a much lower adsorption capacity on KGa-1b compared to that on the other two clays, the adsorption rate constant was the fastest at 0.73 kg/mmol-h. Cation exchange interaction was attributed to the major mechanism for EN adsorption on SWy-2 and IMt-2, and non-electrostatic interactions attributed to EN adsorption when solution pH was above 7. Intercalation of EN molecules into the interlayer space of SWy-2 was confirmed by the XRD patterns after EN adsorption. In contrast, the basal spacing and intensity remained the same after EN adsorption on IMt-2 and KGa-1b, indicating that the EN adsorption on the non-swelling clays were limited to the external surfaces.
1993-08-01
grout is pumped through a central tube in the push rod cable and exits through the probe tip. Retraction grouting (as the rod is withdrawn through the...soil) with a microfine Portland cement grout is normally utilized for all projects; however, subfreezing weather mandated that post - retraction grouting...ELECTRODES (4) P2 RESISTIVITY C2 MODULE GROUTING TUBES (2) 24 IN(61 CM) Grout Injector -- 1.4 IN(3.57 CM) o.D. 0" RINGS GROUTING CONE SLEEVE FRICTION
NASA Astrophysics Data System (ADS)
Marsaglia, K. M.; Carozzi, A. V.
The Basal Salina Formation is a lower Eocene transgressive sequence consisting of interbedded shales, siltstones, and conglomeratic sandstones. This formation occurs in the Talara basin of northwestern Peru and is one of a series of complexly faulted hydrocarbon-producing formations within this extensional forearc basin. These sediments were probably deposited in a fan-delta complex that developed along the ancestral Amotape Mountains during the early Eocene. Most of the sediment was derived from the low-grade metamorphic and plutonic rocks that comprise the Amotape Mountains, and their sedimentary cover. Detrital modes of these sandstones reflect the complex tectonic history of the area, rather than the overall forearc setting. Unlike most forearc sediments, these are highly quartzose, with only minor percentages of volcanic detritus. This sand is variably indurated and cemented by chlorite, quartz, calcite, and kaolinite. Clay-mineral matrix assemblages show gradational changes with depth, from primarily detrital kaolinite to diagenetic chlorite and mixed-layered illite/smectite. Basal Salina sandstones exhibit a paragenetic sequence that may be tied to early meteoric influx or late-stage influx of thermally driven brines associated with hydrocarbon migration. Much of the porosity is secondary, resulting from a first-stage dissolution of silicic constituents (volcanic lithic fragments, feldspar, and fibrous quartz) and a later dissolution of surrounding carbonate cement. Types of pores include skeletal grains, grain molds, elongate pores, and fracture porosity. Measured porosity values range up to 24% and coarser samples tend to be more porous. Permeability is enhanced by fractures and deterred by clay-mineral cements and alteration residues.
In situ clay formation : evaluation of a proposed new technology for stable containment barriers.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Nagy, Kathryn L.; DiGiovanni, Anthony Albert; Fredrich, Joanne T.
2004-03-01
Containment of chemical wastes in near-surface and repository environments is accomplished by designing engineered barriers to fluid flow. Containment barrier technologies such as clay liners, soil/bentonite slurry walls, soil/plastic walls, artificially grouted sediments and soils, and colloidal gelling materials are intended to stop fluid transport and prevent plume migration. However, despite their effectiveness in the short-term, all of these barriers exhibit geochemical or geomechanical instability over the long-term resulting in degradation of the barrier and its ability to contain waste. No technologically practical or economically affordable technologies or methods exist at present for accomplishing total remediation, contaminant removal, or destruction-degradationmore » in situ. A new type of containment barrier with a potentially broad range of environmental stability and longevity could result in significant cost-savings. This report documents a research program designed to establish the viability of a proposed new type of containment barrier derived from in situ precipitation of clays in the pore space of contaminated soils or sediments. The concept builds upon technologies that exist for colloidal or gel stabilization. Clays have the advantages of being geologically compatible with the near-surface environment and naturally sorptive for a range of contaminants, and further, the precipitation of clays could result in reduced permeability and hydraulic conductivity, and increased mechanical stability through cementation of soil particles. While limited success was achieved under certain controlled laboratory conditions, the results did not warrant continuation to the field stage for multiple reasons, and the research program was thus concluded with Phase 2.« less
Microstructural controls on the macroscopic behavior of geo-architected rock samples
NASA Astrophysics Data System (ADS)
Mitchell, C. A.; Pyrak-Nolte, L. J.
2017-12-01
Reservoir caprocks, are known to span a range of mechanical behavior from elastic granitic units to visco-elastic shale units. Whether a rock will behave elastically, visco-elastically or plastically depends on both the compositional and textural or microsctructural components of the rock, and how these components are spatially distributed. In this study, geo-architected caprock fabrication was performed to develop synthetic rock to study the role of rock rheology on fracture deformations, fluid flow and geochemical alterations. Samples were geo-architected with Portland Type II cement, Ottawa sand, and different clays (kaolinite, illite, and Montmorillonite). The relative percentages of these mineral components are manipulated to generate different rock types. With set protocols, the mineralogical content, texture, and certain structural aspects of the rock were controlled. These protocols ensure that identical samples with the same morphological and mechanical characteristics are constructed, thus overcoming issues that may arise in the presence of heterogeneity and high anisotropy from natural rock samples. Several types of homogeneous geo-architected rock samples were created, and in some cases the methods were varied to manipulate the physical parameters of the rocks. Characterization of rocks that the samples exhibit good repeatability. Rocks with the same mineralogical content generally yielded similar compressional and shear wave velocities, UCS and densities. Geo-architected rocks with 10% clay in the matrix had lower moisture content and effective porosities than rocks with no clay. The process by which clay is added to the matrix can strongly affect the resulting compressive strength and physical properties of the geo-architected sample. Acknowledgment: This material is based upon work supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Geosciences Research Program under Award Number (DE-FG02-09ER16022).
DOT National Transportation Integrated Search
2013-10-01
A significant proportion of the United States bridge inventory is based on bonded post-tensioned (PT) concrete construction. An important aspect of maintaining corrosion protection of these PT systems is assuring that tendon ducts are properly groute...
DOT National Transportation Integrated Search
2013-10-01
"A significant proportion of the U.S. bridge inventory is based on bonded post-tensioned (PT) concrete construction. An : important aspect of maintaining corrosion protection of these PT systems is assuring that tendon ducts are properly grouted : wi...
Soil forensics: How far can soil clay analysis distinguish between soil vestiges?
Corrêa, R S; Melo, V F; Abreu, G G F; Sousa, M H; Chaker, J A; Gomes, J A
2018-03-01
Soil traces are useful as forensic evidences because they frequently adhere to individuals and objects associated with crimes and can place or discard a suspect at/from a crime scene. Soil is a mixture of organic and inorganic components and among them soil clay contains signatures that make it reliable as forensic evidence. In this study, we hypothesized that soils can be forensically distinguished through the analysis of their clay fraction alone, and that samples of the same soil type can be consistently distinguished according to the distance they were collected from each other. To test these hypotheses 16 Oxisol samples were collected at distances of between 2m and 1.000m, and 16 Inceptisol samples were collected at distances of between 2m and 300m from each other. Clay fractions were extracted from soil samples and analyzed for hyperspectral color reflectance (HSI), X-ray diffraction crystallographic (XRD), and for contents of iron oxides, kaolinite and gibbsite. The dataset was submitted to multivariate analysis and results were from 65% to 100% effective to distinguish between samples from the two soil types. Both soil types could be consistently distinguished for forensic purposes according to the distance that samples were collected from each other: 1000m for Oxisol and 10m for Inceptisol. Clay color and XRD analysis were the most effective techniques to distinguish clay samples, and Inceptisol samples were more easily distinguished than Oxisol samples. Soil forensics seems a promising field for soil scientists as soil clay can be useful as forensic evidence by using routine analytical techniques from soil science. Copyright © 2017 The Chartered Society of Forensic Sciences. Published by Elsevier B.V. All rights reserved.
NASA Astrophysics Data System (ADS)
Wang, Hua
2018-02-01
In the mine construction, the surface pre-grouting technology is an important method to prevent water blast in excavation process of vertical shaft when the shaft must pass through the thick, water-rich and high water-pressure bedrock aquifer. It has been nearly 60 years since the technology was used to reform wall rock of vertical shaft in coal mine in China for the first time, and the existing technology can basically meet the needs of constructing 1000m deep vertical shaft. Firstly, the article introduces that in view of Magg’s spherical seepage theory and Karol’s spherical seepage theory, Chinese scholars found that the diffusion of grout from borehole into the surrounding strata in horizontal direction is irregular through a lot of research and engineering practice of using the surface pre-grouting technology to reform wall rock of vertical shafts, and put forward the selecting principles of grout’s effective diffusion radius in one grouting engineering; Secondly, according to the shape of the grouting boreholes, surface pre-grouting technology of vertical shaft is divided into two stages: vertical borehole stage and S-type borehole stage. Thirdly, the development status of grouting materials and grouting equipment for the technology is introduced. Fourthly, grouting mode, stage height and pressure of the technology are introduced. Finally, it points out that with the increasing depth of coal mining in China, the technology of reforming wall rock of 1000~2000m deep vertical shafts will face many problems, such as grouting theory, grouting equipment, grouting finishing standard, testing and evaluation of grouting effect, and so on. And it put forward a preliminary approach to solving these problems. This paper points out future research directions of the surface pre-grouting technology in China.
NASA Astrophysics Data System (ADS)
Smith, L. A.; Barbour, S. L.; Hendry, M. J.; Novakowski, K.; van der Kamp, G.
2016-07-01
Characterizing the hydraulic conductivity (K) of aquitards is difficult due to technical and logistical difficulties associated with field-based methods as well as the cost and challenge of collecting representative and competent core samples for laboratory analysis. The objective of this study was to produce a multiscale comparison of vertical and horizontal hydraulic conductivity (Kv and Kh, respectively) of a regionally extensive Cretaceous clay-rich aquitard in southern Saskatchewan. Ten vibrating wire pressure transducers were lowered into place at depths between 25 and 325 m, then the annular was space was filled with a cement-bentonite grout. The in situ Kh was estimated at the location of each transducer by simulating the early-time pore pressure measurements following setting of the grout using a 2-D axisymmetric, finite element, numerical model. Core samples were collected during drilling for conventional laboratory testing for Kv to compare with the transducer-determined in situ Kh. Results highlight the importance of scale and consideration of the presence of possible secondary features (e.g., fractures) in the aquitard. The proximity of the transducers to an active potash mine (˜1 km) where depressurization of an underlying aquifer resulted in drawdown through the aquitard provided a unique opportunity to model the current hydraulic head profile using both the Kh and Kv estimates. Results indicate that the transducer-determined Kh estimates would allow for the development of the current hydraulic head distribution, and that simulating the pore pressure recovery can be used to estimate moderately low in situ Kh (<10-11 m s-1).
WASTE SOLIDIFICATION BUILDING BENCH SCALE HIGH ACTIVITY WASTE SIMULANT VARIABILITY STUDY FY2008
DOE Office of Scientific and Technical Information (OSTI.GOV)
Hansen, E; Timothy Jones, T; Tommy Edwards, T
2009-03-20
The primary objective of this task was to perform a variability study of the high activity waste (HAW) acidic feed to determine the impact of feed variability on the quality of the final grout and on the mixability of the salt solution into the dry powders. The HAW acidic feeds were processed through the neutralization/pH process, targeting a final pH of 12. These fluids were then blended with the dry materials to make the final waste forms. A secondary objective was to determine if elemental substitution for cost prohibitive or toxic elements in the simulant affects the mixing response, thusmore » providing a more economical simulant for use in full scale tests. Though not an objective, the HAW simulant used in the full scale tests was also tested and compared to the results from this task. A statistically designed test matrix was developed based on the maximum molarity inputs used to make the acidic solutions. The maximum molarity inputs were: 7.39 HNO{sub 3}, 0.11618 gallium, 0.5423 silver, and 1.1032 'other' metals based on their NO{sub 3}{sup -} contribution. Substitution of the elements aluminum for gallium and copper for silver was also considered in this test matrix, resulting in a total of 40 tests. During the NaOH addition, the neutralization/pH adjustment process was controlled to a maximum temperature of 60 C. The neutralized/pH adjusted simulants were blended with Portland cement and zircon flour at a water to cement mass ratio of 0.30. The mass ratio of zircon flour to Portland cement was 1/12. The grout was made using a Hobart N-50 mixer running at low speed for two minutes to incorporate and properly wet the dry solids with liquid and at medium speed for five minutes for mixing. The resulting fresh grout was measured for three consecutive yield stress measurements. The cured grout was measured for set, bleed, and density. Given the conditions of preparing the grout in this task, all of the grouts were visually well mixed prior to preparing the grouts for measurements. All of the cured grouts were measured for bleed and set. All of the cured grouts satisfied the bleed and set requirements, where no bleed water was observed on any of the grout samples after one day and all had set within 3 days of curing. This data indicates, for a well mixed product, bleed and set requirement are satisfied for the range of acidic feeds tested in this task. The yield stress measurements provide both an indication on the mixability of the salt solution with dry materials and an indication of how quickly the grout is starting to form structure. The inability to properly mix these two streams into a well mixed grout product will lead to a non-homogeneous mixture that will impact product quality. Product quality issues could be unmixed regions of dry material and hot spots having high concentrations of americium 241. Mixes that were more difficult to incorporate typically resulted in grouts with higher yield stresses. The mixability from these tests will provide Waste Solidification Building (WSB) an indication of which grouts will be more challenging to mix. The first yield stress measurements were statistically compared to a list of variables, specifically the batched chemicals used to make the acidic solutions. The first yield stress was also compared to the physical properties of the acidic solutions, physical and pH properties of the neutralized/pH adjusted solutions, and chemical and physical properties of the grout.« less
Reservoir assessment of the Nubian sandstone reservoir in South Central Gulf of Suez, Egypt
NASA Astrophysics Data System (ADS)
El-Gendy, Nader; Barakat, Moataz; Abdallah, Hamed
2017-05-01
The Gulf of Suez is considered as one of the most important petroleum provinces in Egypt and contains the Saqqara and Edfu oil fields located in the South Central portion of the Gulf of Suez. The Nubian sandstone reservoir in the Gulf of Suez basin is well known for its great capability to store and produce large volumes of hydrocarbons. The Nubian sandstone overlies basement rocks throughout most of the Gulf of Suez region. It consists of a sequence of sandstones and shales of Paleozoic to Cretaceous age. The Nubian sandstone intersected in most wells has excellent reservoir characteristics. Its porosity is controlled by sedimentation style and diagenesis. The cementation materials are mainly kaolinite and quartz overgrowths. The permeability of the Nubian sandstone is mainly controlled by grain size, sorting, porosity and clay content especially kaolinite and decreases with increase of kaolinite. The permeability of the Nubian Sandstone is evaluated using the Nuclear Magnetic Resonance (NMR technology) and formation pressure data in addition to the conventional logs and the results were calibrated using core data. In this work, the Nubian sandstone was investigated and evaluated using complete suites of conventional and advanced logging techniques to understand its reservoir characteristics which have impact on economics of oil recovery. The Nubian reservoir has a complicated wettability nature which affects the petrophysical evaluation and reservoir productivity. So, understanding the reservoir wettability is very important for managing well performance, productivity and oil recovery.
Study of Usage Areas of Clay Samples of Asphaltite Quarries in Sirnak, Turkey
NASA Astrophysics Data System (ADS)
Bilgin, Oyku
2017-12-01
The asphaltite of Sirnak, Turkey are in the form of 12 veins and their total reserves are anticipated to be approximately 200 million tons in a field of 25.000 hectares. The asphaltites at the Sirnak region are in the form of fault and crack fillings and take place together with clay minerals at their side rock. The main raw materials used in the production of cement are limestone, clay and marn known as sedimentary rocks. Limestone for CaO and clay minerals for SiO2, Al2O3, and Fe2O3, which are the main compounds of clinker production, are the main raw materials. Other materials containing these four oxides like marn are also used as cement raw material. Conformity levels of the raw materials to be used in cement production vary according to their chemical compounds. The rocks to be used as clay mineral are evaluated by taking the rate of silicate and alumina into consideration. The soils suitable for brick-tile productions are named as sandy clay. Their difference from the ceramic clays is that they are richer in terms of iron, silica and carbonate. These soils are also known under the names such as clay, arid, alluvium, silt, loam and argil. Inside these soils, minerals such as quartz, montmorillonite, kaolinite, calcite, limonite, hidromika, sericite, illite, and chlorite are available. Some parts of the soils consist of clays in amorphous structure. Limestone parts, gypsums, organic substances and bulky rock residuals spoil the quality. The soils suitable for brick production may not be suitable for tile production. In this case, their sandy soils should be mixed up with the clays with fine granule structure which is high in plasticity. During asphaltite mining in Sirnak region, clays forming side rock are gathered at dump sites. In this study; SQX analyses of the clay samples taken from Avgamasya, Seridahli and Segürük asphaltite veins run in Sirnak region are carried out and their usage areas are searched.
The Physical Behavior of Stabilised Soft Clay by Electrokinetic Stabilisation Technology
NASA Astrophysics Data System (ADS)
Azhar, A. T. S.; Nordin, N. S.; Azmi, M. A. M.; Embong, Z.; Sunar, N.; Hazreek, Z. A. M.; Aziman, M.
2018-04-01
Electrokinetic Stabilisation (EKS) technology is the combination processes of electroosmosis and chemical grouting. This technique is most effective in silty and clayey soils where the hydraulic conductivity is very low. Stabilising agents will assist the EKS treatment by inducing it into soil under direct current. The movement of stabilising agents into soil is governed by the principle of electrokinetics. The aim of this study is to evaluate the physical behavior of soft soil using the EKS technology as an effective method to strengthen soft clay soils with calcium chloride (CaCl2) as the stabilising agent. Stainless steel plates were used as the electrodes, while 1.0 mol/l of CaCl2 was used as the electrolyte that fed at the anode compartment. Soft marine clay at Universiti Tun Hussein Onn Malaysia was used as the soil sample. The EKS treatment was developed at Research Centre for Soft Soil (RECESS), UTHM with a constant voltage gradient (50 V/m) in 21 days. The result shows that the shear strength of treated soil was increased across the soil sample. The treated soil near the cathode showed the highest value of shear strength (24.5 – 33 kPa) compared with the anode and in the middle of the soil sample.
NASA Astrophysics Data System (ADS)
Kent, D. V.; Lanci, L.; Wang, H.; Wright, J.
2017-12-01
Wilson Lake B and Millville are the two core sites on the NJ Coastal Plain where an impact spherule layer was discovered at the base of the Marlboro Clay, coinciding with the onset of the carbon isotope excursion (CIE) that identifies the Paleocene-Eocene boundary (Schaller+2016 Science). At the more proximal Wilson Lake site ( 35 m paleowater depth, 20 km from the paleoshore), enhanced magnetization of the Marlboro Clay marked by a dramatic increase in concentration of submicron magnetic particles closely coincided with the sharp peak in abundance of the spherules (Kent+2017 EPSL). Discounting magnetotactic bacteria and impact plume condensate as significant sources of the magnetic nanoparticles that dominate the magnetization of the 10 m-thick Marlboro Clay, a pyrogenetic origin was postulated whereby a widespread and intense conflagration over the hinterlands, quite possibly impact-induced, produced magnetic nanoparticles in the heated soils, a process long known from wildfires and laboratory heating experiments. The pyromagnetically-enhanced kaolinite-rich soils would have been swept from the denuded landscape and deposited across the adjoining shelf, perhaps as mudwaves, to become the Marlboro Clay. The Millville site at double the paleowater depth and distance to the paleoshore compared to Wilson Lake (Makarova+2017 Paleoceanography) shows a similar enhancement in magnetization of the Marlboro Clay. However, the increase in magnetization in Millville starts well above ( 50 cm) the spherule peak and the onset of the CIE, which coincide with a sharp drop in what little carbonate content there is in the Marlboro Clay, resulting in a zone barren of foraminifers (Makarova+2017 op. cit.). The offset in deposition might be due to added barren zone or a longer transit of the soil muds to the more distant Millville site but would not be expected if the magnetic nanoparticles were produced in more direct response to the onset of the CIE, as from proliferation of magnetotactic bacteria. The pyromagnetic enhancement of soils and their (re)deposition can be viewed as local manifestations of a major event that triggered various global reverberations. For example, there is no counterpart of the Marlboro Clay in ODP Site 1051 on Blake Nose where a spherule layer was also found at the onset of the CIE (Schaller+2016 op. cit.).
Thermally conductive cementitious grout for geothermal heat pump systems
Allan, Marita
2001-01-01
A thermally conductive cement-sand grout for use with a geothermal heat pump system. The cement sand grout contains cement, silica sand, a superplasticizer, water and optionally bentonite. The present invention also includes a method of filling boreholes used for geothermal heat pump systems with the thermally conductive cement-sand grout. The cement-sand grout has improved thermal conductivity over neat cement and bentonite grouts, which allows shallower bore holes to be used to provide an equivalent heat transfer capacity. In addition, the cement-sand grouts of the present invention also provide improved bond strengths and decreased permeabilities. The cement-sand grouts can also contain blast furnace slag, fly ash, a thermoplastic air entraining agent, latex, a shrinkage reducing admixture, calcium oxide and combinations thereof.
Laboratory Testing of Silica Sol Grout in Coal Measure Mudstones.
Pan, Dongjiang; Zhang, Nong; Xie, Zhengzheng; Feng, Xiaowei; Kong, Yong
2016-11-22
The effectiveness of silica sol grout on mudstones is reported in this paper. Using X-ray diffraction (XRD), the study investigates how the silica sol grout modifies mudstone mineralogy. Micropore sizes and mechanical properties of the mudstone before and after grouting with four different materials were determined with a surface area/porosity analyser and by uniaxial compression. Tests show that, after grouting, up to 50% of the mesopore volumes can be filled with grout, the dominant pore diameter decreases from 100 nm to 10 nm, and the sealing capacity is increased. Uniaxial compression tests of silica sol grouted samples shows that their elastic modulus is 21%-38% and their uniaxial compressive strength is 16%-54% of the non-grouted samples. Peak strain, however, is greater by 150%-270%. After grouting, the sample failure mode changes from brittle to ductile. This paper provides an experimental test of anti-seepage and strengthening properties of silica sol.
NASA Astrophysics Data System (ADS)
Liu, Quansheng; Lei, Guangfeng; Peng, Xingxin; Lu, Chaobo; Wei, Lai
2018-02-01
Grouting reinforcement, which has an obvious strengthening effect on fractured rock mass, has been widely used in various fields in geotechnical engineering. The rheological properties of grout will greatly affect its diffusion radius in rock fractures, and the water-cement ratio is an important factor in determining the grouting flow patterns. The relationship between shear stress and shear rate which could reflect the grout rheological properties, the effects of water-cement ratio, and temperature on the rheological properties of grouting was studied in the laboratory. Besides, a new method for producing fractured rock specimens was proposed and solved the problem of producing natural fractured rock specimens. To investigate the influences of grouting on mechanical properties of a rock fracture, the fractured rock specimens made using the new method were reinforced by grouting on the independent designed grouting platform, and then normal and tangential mechanical tests were carried out on fractured rock specimens. The results showed that the mechanical properties of fractured rock mass are significantly improved by grouting, the peak shear strength and residual strength of rock fractures are greatly improved, and the resistance to deformation is enhanced after grouting. Normal forces affect the tangential behavior of the rock fracture, and the tangential stress strength increases with normal forces. The strength and stability of fractured rock mass are increased by grouting reinforcement.
1985-02-20
Surface Cemennt/entonte Grout Rat 20/1 6" Diameter Bore "Ole 8 Foit B.G.S. Bentorito 4" Diameter POes" Schedle 409 Fee S.O.S.PVC Riser Pipe with...Casing with Locking Cap GRiser Pipe StickupGround Surface 2.2Fe Cement/BSentonite Grout Ratio 20/1 8" Diameter Bore Hole cv Ile- 3 Feet B.G.S...Ground Surface 4’. Ground Surface .0~ Cemtert/Bentonlte Grout Rat 20/1 8" Diamneter Bore Hole__ 4" Diameter Pl O Schedule 404 PVC Riser Pipe FetBGS
NASA Astrophysics Data System (ADS)
Dafny, Elad; Tawfeeq, Kochar Jamal; Ghabraie, Kazem
2015-10-01
Dam sites provide an outstanding opportunity to explore dynamic changes in the groundwater flow regime because of the high hydraulic gradient rapidly induced in their surroundings. This paper investigates the temporal changes of the hydraulic conductivities of the rocks and engineered structures via a thorough analysis of hydrological data collected at the Dokam Dam, Iraq, and a numerical model that simulates the Darcian component of the seepage. Analysis of the data indicates increased seepage with time and suggests that the hydraulic conductivity of the rocks increased as the conductivity of the grout curtain decreased. Conductivity changes on the order of 10-8 m/s, in a 20-yr period were quantified using the numerical analysis. It is postulated that the changes in hydraulic properties in the vicinity of Dokan Dam are due to suspension of fine materials, interbedded in small fissures in the rocks, and re-settlement of these materials along the curtain. Consequently, the importance of the grout curtain to minimize the downstream seepage, not only as a result of the conductivity contrast with the rocks, but also as a barrier to suspended clay sediments, is demonstrated. The numerical analysis also helped us to estimate the proportion of the disconnected karstic conduit flow to the overall flow.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Lee, Si Y.; Hyun, Sinjae
2013-01-10
A new disposal unit, designated as Saltstone Disposal Unit 6 (SDU6), is being designed for support of site accelerated closure goals and salt waste projections identified in the new Liquid Waste System Plan. The unit is a cylindrical disposal cell of 375 ft in diameter and 43 ft in height, and it has a minimum 30 million gallons of capacity. SRNL was requested to evaluate the impact of an increased grout placement height on the flow patterns radially spread on the floor and to determine whether grout quality is impacted by the height. The primary goals of the work aremore » to develop the baseline Computational Fluid Dynamics (CFD) model and to perform the evaluations for the flow patterns of grout material in SDU6 as a function of elevation of grout discharge port and grout rheology. Two transient grout models have been developed by taking a three-dimensional multiphase CFD approach to estimate the domain size of the grout materials radially spread on the facility floor and to perform the sensitivity analysis with respect to the baseline design and operating conditions such as elevation height of the discharge port and fresh grout properties. For the CFD modeling calculations, air-grout Volume of Fluid (VOF) method combined with Bingham plastic and time-dependent grout models were used for examining the impact of fluid spread performance for the initial baseline configurations and to evaluate the impact of grout pouring height on grout quality. The grout quality was estimated in terms of the air volume fraction for the grout layer formed on the SDU6 floor, resulting in the change of grout density. The study results should be considered as preliminary scoping analyses since benchmarking analysis is not included in this task scope. Transient analyses with the Bingham plastic model were performed with the FLUENTTM code on the high performance parallel computing platform in SRNL. The analysis coupled with a transient grout aging model was performed by using ANSYS-CFX code in the parallel computing platform in Mercer University. Recommended operational guidance was developed assuming that local shear rates and flow patterns related to radial spread along the SDU floor can be used as a measure of grout performance and spatial dispersion affected by the grout height and viscosity. The 5 ft height baseline results show that when the 150 gpm grout flow with a 5 Pa yield stress and a 60 cp viscosity is poured down through a 3 inch discharge port, the grout is spread radially up to about 64 ft distance from the pouring center after 2 hours' pouring time. The air volume fraction of the grout layer is about 29% at 5 minutes' transient time, and it is reduced by about 9% in 2 hours' pouring time, resulting in the grout density consisting of about 80% grout and 20% air volume fractions. The sensitivity results show that when the discharge port is located at a higher position, a larger amount of air is trapped inside the layer formed below the discharge port at the early transient time of less than 30 minutes because of the higher impinging momentum of the grout flow on the floor, resulting in the formation of less smooth layer. The results clearly indicate that the radial spread for the 43 ft discharge port is about 10% faster than that of the 5 ft discharge port for the early transient period of 5 minutes. However, for the pouring time longer than half an hour, the discharge port height does not affect the radial distance spread on the disposal floor. When grout quality is related to grout volume fraction, the grout volume fraction for the 43 ft discharge port has lower volume fraction than the 5 ft discharge port for the transient period of the first 5 minutes. However, for the pouring time longer than half an hour, the discharge port height does not affect the grout volume fraction for the layer accumulated on the disposal floor. A modified Bingham plastic model coupled with time-dependent viscosity behavior was developed for conducting the initial scoping calculations to assess the impact of fluid residence time on radial spreading and basic flow patterns. The results for the transient viscosity model show that when grout material becomes more viscous, the thickness of the grout layer accumulated on the floor becomes higher, but the radial distance spread on the horizontal floor becomes smaller. The early transient results for the grout density with about 32% air volume fractions are in reasonable agreement with those of the idealized Bingham plastic model. It is recommended that the current models developed here be benchmarked against the experimental results for critical applications of the modeling results.« less
NASA Astrophysics Data System (ADS)
Moussa, Abderamane; Novello, Alice; Lebatard, Anne-Elisabeth; Decarreau, Alain; Fontaine, Claude; Barboni, Doris; Sylvestre, Florence; Bourlès, Didier L.; Paillès, Christine; Buchet, Guillaume; Duringer, Philippe; Ghienne, Jean-François; Maley, Jean; Mazur, Jean-Charles; Roquin, Claude; Schuster, Mathieu; Vignaud, Patrick; Brunet, Michel
2016-06-01
This study presents mineralogical and geochemical data from a borehole drilled near the locality of Bol (13°27‧N, 14°44‧E), in the eastern archipelago of the modern Lake Chad (Chad). Samples were taken from a ∼200 m long core section forming a unique sub-continuous record for Central Africa. Among these samples, 25 are dated between 6.4 and 2.4 Ma. Dominant minerals are clays (66% average) mixed with varying amounts of silt and diatomite. The clay fraction consists of Fe-beidellite (87% average), kaolinite, and traces of illite. Clay minerals originate from the erosion of the vertisols that surrounded the paleolake Chad. Sedimentological data indicate that a permanent lake (or recurrent lakes) existed from 6.7 until 2.4 Ma in the vicinity of Bol. By comparison with modern latitudinal distribution of vertisols in Africa the climate was Sudanian-like. Changes in the sedimentation rate suggest a succession of wetter and dryer periods during at least six million years in the region during the critical time period covering the Miocene-Pliocene transition.
Laboratory Testing of Silica Sol Grout in Coal Measure Mudstones
Pan, Dongjiang; Zhang, Nong; Xie, Zhengzheng; Feng, Xiaowei; Kong, Yong
2016-01-01
The effectiveness of silica sol grout on mudstones is reported in this paper. Using X-ray diffraction (XRD), the study investigates how the silica sol grout modifies mudstone mineralogy. Micropore sizes and mechanical properties of the mudstone before and after grouting with four different materials were determined with a surface area/porosity analyser and by uniaxial compression. Tests show that, after grouting, up to 50% of the mesopore volumes can be filled with grout, the dominant pore diameter decreases from 100 nm to 10 nm, and the sealing capacity is increased. Uniaxial compression tests of silica sol grouted samples shows that their elastic modulus is 21%–38% and their uniaxial compressive strength is 16%–54% of the non-grouted samples. Peak strain, however, is greater by 150%–270%. After grouting, the sample failure mode changes from brittle to ductile. This paper provides an experimental test of anti-seepage and strengthening properties of silica sol. PMID:28774061
Comparing the shear strength of grouted fractures: conventional methods vs biomineralisation
NASA Astrophysics Data System (ADS)
El Mountassir, G.; Tobler, D. J.; Moir, H.; Lunn, R. J.; Phoenix, V. R.
2011-12-01
For many engineering applications, such as geological disposal of nuclear waste, underground railways etc., it is necessary to limit fluid flow through fractures. The particle size of conventional cementitious grouts limits the size of fractures into which they can penetrate. To address this issue increasingly microfine and ultrafine cement grouts are becoming commercially available. Despite this the radius of penetration remains dependent on the grout viscosity alongside injection pressure, pumping rate, grout setting time and grout cohesion. As such lower viscosity aqueous solutions may have a greater radius of penetration potentially requiring fewer injection points. In addition cementitious grouts typically undergo volumetric shrinkage during setting. In many applications this change in volume may not be of particular importance but in others where a very low hydraulic conductivity is a critical design criterion, as in nuclear waste repositories, this reduction in volume may be highly significant. This study investigates the use of microbially induced carbonate precipitation (MCP) as a technique for grouting fine aperture rock fractures. Artificial fractures were created in granite cores and were subjected to conventional cementitious grouting methods and MCP. Following treatment the hydraulic and mechanical properties of the grouted fractures were investigated. The mechanical properties of grouts after setting is not usually considered to be a significant issue, but in applications which consider much longer timescales (100,000 years) grouts which result in fractures with improved strength and lower hydraulic conductivity are likely to be preferred.
NASA Astrophysics Data System (ADS)
Aminul Islam, M.
2009-06-01
This study deals with the diagenesis and reservoir quality of sandstones of the Bhuban Formation located at the Titas Gas Field of Bengal Basin. Petrographic study including XRD, CL, SEM and BSE image analysis and quantitative determination of reservoir properties were carried out for this study. The sandstones are fine to medium-grained, moderately well to well sorted subfeldspathic arenites with subordinate feldspathic and lithic arenites. The diagenetic processes include clay infiltration, compaction and cementation (quartz overgrowth, chlorite, kaolinite, calcite and minor amount of pyrite, dolomite and K-feldspar overgrowth). Quartz is the dominant pore occluding cement and generally occurred as small euhedral crystals, locally as large pyramidal crystals in the primary pores. Pressure solution derived from grain contact is the main contributor of quartz overgrowths. Chlorite occurs as pore-lining and pore filling cement. In some cases, chlorite helps to retain porosity by preventing quartz overgrowth. In some restricted depth interval, pore-occlusion by calcite cement is very much intense. Kaolinite locally developed as vermiform and accelerated the minor porosity loss due to pore-occlusion. Kaolinite/chlorite enhances ineffective microporosity. Kaolinite is a by-product of feldspar leaching in the presence of acidic fluid produced during the maturation of organic matter in the adjacent Miocene or deeper Oligocene source rocks. The relation between diagenesis and reservoir quality is as follows: the initial porosity was decreased by compaction and cementation and then increased by leaching of the metastable grains and dissolution of cement. Good quality reservoir rocks were deposited in fluvial environment and hence quality of reservoir rocks is also environment selective. Porosity and permeability data exhibit good inverse correlation with cement. However, some data points indicate multiple controls on permeability. Reservoir quality is thus controlled by pore occluding cement, textural parameters (grain size, pore size and sorting) and depositional environment. The reservoir finally resumed partly its pre-cementation quality after development of secondary porosity.
Jung, Bahngmi; O'Carroll, Denis; Sleep, Brent
2014-10-15
The introduction of nanoscale zero valent iron (nZVI) into the subsurface has recently received significant attention as a potentially effective method for remediation of source zones of chlorinated solvents present as dense nonaqueous phase liquids (DNAPL). One of the challenges in the deployment of nZVI is to achieve good subsurface nZVI mobility to permit delivery of the nZVI to the target treatment zone. Stabilization of nZVI with various polymers has shown promise for enhancing nZVI subsurface mobility, but the impact of subsurface conditions on nZVI mobility has not been fully explored. In this study, the effect of humic acid and kaolinite on the transport of polymer-stabilized nZVI (carboxylmethyl cellulose-surface modified nZVI, CMC90K-RNIP) in sand was investigated using column experiments. In addition, effects of electrolytes on the stability of CMC90K-RNIP in the presence of humic acid, and the stability of humic acid-coated reactive nanoscale iron particles (HA-RNIP) at various humic acid concentrations were investigated. Humic acid enhanced the mobility of bare RNIP, whereas the transport of CMC90K-RNIP was not significantly affected by humic acid injected as a background solution, except at the highest concentration of 500mg/L. At lower pore water velocity, the effect of humic acid on the transport of CMC90K-RNIP was greater than that at high water velocity. Adding kaolinite up to 2% by weight to the sand column reduced the retention of CMC90K-RNIP, but further increases in kaolinite content (to 5%) did not significantly affect nZVI retention. The impact of kaolinite on nZVI retention was more pronounced at lower pore water velocities. Copyright © 2014 Elsevier B.V. All rights reserved.
NASA Astrophysics Data System (ADS)
Powars, D. S.; Edwards, L. E.; Kopp, R. E.; Self-Trail, J.; Schultz, A.
2009-12-01
Abrupt sedimentary changes mark the Paleocene-Eocene Thermal Maximum (PETM) in the mid-Atlantic Coastal Plain. Across the tectonic downwarp known as the Salisbury Embayment (southeastern Virginia to central New Jersey), kaolinite-rich clay (the Marlboro Clay) abruptly replaces glauconite-rich quartz sand, silt, and illite-smectite clay of the late Paleocene. Dozens of cored boreholes obtained by the USGS and other Federal and State agencies, together with geophysical logs from more than 100 boreholes, allow us to document the widespread distribution and depositional, biostratigraphic, paleoecologic, taphonomic, and tectonic characteristics of the Marlboro Clay. In Maryland and Virginia, the Marlboro Clay is a silvery-gray to pale-red plastic clay and locally includes thin laminations and thicker beds of silt, concretions, pyrite nodules, and rare shell fragments (in downdip cores). The clay is unconformity bounded with highly burrowed contacts. The lower contact is locally so bioturbated that it has been reported as gradational. The upper contact in Virginia has glauconite-rich, sand-filled burrows from the overlying Nanjemoy Formation (lower Eocene) that penetrate as much as 8.5 m down into the Marlboro Clay (total thickness only 9 m). Biostratigraphically, the Marlboro Clay is placed in calcareous nannofossil Zone NP9 (and NP10 in downdip cores) and includes the PETM marker dinocyst species Apectodinium augustum (in downdip cores). In New Jersey, a similar clay deposit is described from the subsurface; and based on consistency in lithology, biostratigraphy, stratigraphic position, isotopic composition and its magnetic properties, we apply the name Marlboro Clay to this unique clay unit throughout the Salisbury Embayment. Structure-contour and isopach maps of the present configuration of the Marlboro Clay reveal a widespread deposit with localized truncation or thinning. Tectonic folding and faulting along the inner Coastal Plain and along the James River structural zone produced syn- and post-depositional erosional thinning on uplifted sides of faults and thickening in downdropped areas. The Chesapeake Bay Impact Structure (CBIS) removed the Marlboro Clay across a large area of southeastern Virginia. Faults and folds associated with the CBIS appear to deform the clay in an outer-fracture-zone that extends up to 25-km outside the crater’s outer rim. The Marlboro Clay thickens and is slightly finer-grained in the deeper part of the Marlboro basin in where structure contours on the top-of-basement generally mimic the tectonic downwarp. The apparent deepest (>200 m below sea level) and thickest (>14 m) part of the Marlboro depositional basin appears to extend from just south of the mouth of the Potomac River northward to the lower Choptank River valley, Maryland, then turns sharply northeastward to beneath the central part of Delaware Bay. The Marlboro Clay of the mid-Atlantic United States thus provides a widespread deposit that in its regional and tectonic setting records, in its unusual sedimentary properties, the severe regional environmental changes associated with global climate change during the PETM.
NASA Astrophysics Data System (ADS)
Verstrynge, E.; Wevers, M.; Ghiassi, B.; Lourenço, P. B.
2016-01-01
Different types of strengthening systems, based on fiber reinforced materials, are under investigation for external strengthening of historic masonry structures. A full characterization of the bond behavior and of the short- and long-term failure mechanisms is crucial to ensure effective design, compatibility with the historic substrate and durability of the strengthening solution. Therein, non-destructive techniques are essential for bond characterization, durability assessment and on-site condition monitoring. In this paper, the acoustic emission (AE) technique is evaluated for debonding characterization and localization on fiber reinforced polymer (FRP) and steel reinforced grout-strengthened clay bricks. Both types of strengthening systems are subjected to accelerated ageing tests under thermal cycles and to single-lap shear bond tests. During the reported experimental campaign, AE data from the accelerated ageing tests demonstrated the thermal incompatibility between brick and epoxy-bonded FRP composites, and debonding damage was successfully detected, characterized and located. In addition, a qualitative comparison is made with digital image correlation and infrared thermography, in view of efficient on-site debonding detection.
Suppression of prairie grasses due to excess magnesium in a portion of a restored prairie.
Franson, Raymond; Krabbe, Stephen; Scholes, Chad
2017-01-02
In June 2002, the Department of Energy (DOE) began establishing the 60 ha Howell Prairie at the DOE Weldon Spring Site (WSS). In one area, the clay base is different from the other soil (subarea 2C). Vegetation sampling was conducted on four permanent plots across the prairie beginning in 2008, and shows that three of the four plots have strong establishment of native prairie species including prairie grasses. The fourth plot (subarea 2C), where the soil is different, shows significantly less native grass cover and stunted vegetation compared to the other three plots. One hundred twenty-five soil samples were taken in 6 different months and in 6 different years across the entire prairie restoration. Across the prairie, potassium (K) and phosphorus (P) were not limiting. The pH, organic matter content (OM), and cation exchange capacity (CEC) did not show trends related to the vegetation issues in subarea 2C. Ordination of the ratio of magnesium (Mg):K shows that Mg is very high in subarea 2C, which has been demonstrated to suppress the growth of prairie grasses. Subarea 2C contains interstratified kaolinite-smectite clay which contributes Mg to soil. It is hypothesized that an inexpensive, nondestructive treatment (addition of K) could be applied to remediate this area.
Development of a polymetric grout for the hydrostatic bearing at DSS 14
NASA Technical Reports Server (NTRS)
Mcclung, C. E.; Schwendeman, J. L.; Ball, G. L., III; Jenkins, G. H.; Casperson, R. D.; Gale, G. P.; Riewe, A. A.
1981-01-01
Results of an investigation into the causes of the deterioration and premature failure of the grout under the hydrostatic bearing runner at DSS 14 are reported. Generic types of materials were screened and tested to find a grout material more resistive to the causes of grout failure. Emphasis was placed on the physical properties, strength, modulus of elasticity, and resistance to erosion and chemical attack by oil and unique requirements imposed by each material for mixing, placing, compacting, and cooling. The polymetric grout developed to replace the dry grout is described.
NASA Astrophysics Data System (ADS)
Melo, Mário Sérgio de; Guimarães, Gilson Burigo; Chinelatto, Adilson Luiz; Giannini, Paulo César Fonseca; Pontes, Henrique Simão; Chinelatto, Adriana Scoton Antonio; Atencio, Daniel
2015-11-01
Karstification processes in sandstones of the Furnas Formation, Silurian to Devonian of the Paraná Basin, have been described since the mid-twentieth century. However, some geologists still doubt the idea of true karst in sandstones. Studies carried out in the Campos Gerais region, Paraná State, Southern Brazil, aimed at investigating the nature of erosion processes in Furnas Formation and the role of the dissolution in the development of their notorious erosive features and underground cavities. These studies have led to the recognition of dissolution macro to micro features ('furnas', caves, ponds, sinks, ruiniform relief on cliffs and rocky surfaces, grain corrosion, speleothems, mineral reprecipitation and incrustation). The analysis (scanning electron microscopy, energy dispersive spectrometry and x-ray diffractometry) of sandstones and their alterites has indicated significant dissolution of clay cement along with discrete quartz grain dissolution. This mesodiagenetic cement (kaolinite and illite) is dissolved and reprecipitated as clay minerals with poorly developed crystallinity along with other minerals, such as variscite and minerals of the alunite supergroup, suggesting organic participation in the processes of dissolution and incrustation. The mineral reprecipitation usually forms centimetric speleothems, found in cavities and sheltered rocky surfaces. The cement dissolution associated with other factors (fractures, wet weather, strong hydraulic gradient, antiquity of the landforms) leads to the rock arenisation, the underground erosion and the appearance of the karst features. Carbonate rocks in the basement may locally be increasing the karst forms in the overlying Furnas Formation. The recognition of the karst character of the Furnas Formation sandstones has important implications in the management of underground water resources (increasingly exploited in the region), in the use of the unique geological heritage and in the prevention of geo-environmental accidents resulting from underground erosion phenomena.
Abiogenic photochemical synthesis on surface of meteorites and other small space bodies
NASA Astrophysics Data System (ADS)
Simakov, Michael B.; Kuzicheva, Eugenia A.
The abiogenic photochemical synthesis of complex biochemical compounds on the surface of small bodies in our Solar system was examined. Hydrated minerals are found within a chondrite matrix of meteorites together with significant amounts of organic matter. Clays are likely to have formed when water was present on parent meteoritic bodies. In order to verify the existence of a relationship between abiogenic synthesis of nucleotides and inorganic components of the meteorites, we have investigated possible abiogenic reactions associated with different clay (montmorillonite, kaolinite) and a basaltic one (Tyatya's volcanic ash) under action of open space energy sources as a model of different exobiological environments on the surface of small space bodies. The abiogenic synthesis of natural adenine nucleotides from a mixture of adenosine and inorganic phosphate has been observed following irradiation with VUV light in the presence of different mineral samples. The yields of the products (5'AMP, 2'AMP, 3'AMP, 2'3'cAMP and 3'5'cAMP) depended on irradiation time and kinds of minerals used. The discovery that meteoritic organic compounds may be trapped and protected within a clay mineral matrix has implications for our understanding of prebiotic molecular evolution in the early Solar system. Clay minerals may also have concentrated organic compounds thereby promoting polymerization reactions. An adsorption/binding of nucleic acids components by clay crystals could change the electron distribution and/or the conformation of the molecules. The remnant water molecules in the clay sheets also could influence the course of the reaction. Clay immobilization of phosphate could play an important role in this reaction. Chondritic material could have been a common component of the inner Solar system shortly after its formation and the biologically useful products of clay mineral-organic matter interactions could have also widespread, and delivered to planetary surfaces through the accretion of carbonaceous asteroids.
An abiogenic photochemical synthesis on surface of meteorites and other small space bodies
NASA Astrophysics Data System (ADS)
Simakov, M.; Kuzicheva, E.
Abiogenic photochemical synthesis of complex biochemical compounds on the surface of small bodies in our Solar system was examined. The hydrated minerals are found within a chondrite matrix of meteorites together with significant amounts of organic matter. Clays are likely to have formed when water was presented on parent meteoritic bodies. In order to verify the existence of a relationship between abiogenic synthesis of nucleotides and inorganic components of the meteorites we have investigated possible abiogenic reactions at the presence of different clay minerals (montmorillonite, kaolinite) and basaltic sample (Tjatja's volcanic ash) under action of open space energy sources for modeling of different exobiological environments on the surface of small space bodies. The abiogenic synthesis of natural adenine nucleotides from mixture of adenosine plus inorganic phosphate has been observed under an irradiation with VUV radiation at the presence of different mineral samples. The yields of the products (5'AMP, 2'AMP, 3'AMP, 2'3'cAMP and 3'5'cAMP) were depended from irradiation time and kind of used minerals. The discovery that meteoritic organic compounds may be trapped and protected within a clay mineral matrix has implications for our understanding of prebiotic molecular evolution in the early Solar system. Clay minerals may have concentrated organic compounds thereby promoting polymerization reactions also. An adsorption/binding of nucleic acids components by clay crystals could change in the electron distribution and/or the conformation of the molecules. The remnant water molecules in the clay sheets also could influence on the course of the reaction. Besides, an immobilization of phosphate on clay also could play an important role in our reaction. Chondritic material would have been a common component of the inner Solar system shortly after its formation and the biologically useful products of clay mineral-organic matter interactions would have also widespread, and delivered to planetary surfaces through the accretion of carbonaceous asteroids.
Design and Control of Chemical Grouting : Volume 3 - Engineering Practice
DOT National Transportation Integrated Search
1983-04-01
Recent improvements in the engineering practice of chemical grouting have provided increased confidence in this method of ground modification. Designers can significantly improve the success of chemical grouting by defining their grouting program obj...
MINERALOGY, PETROGRAPHY, AND RADIOACTIVITY OF REPRESENTATIVE SAMPLES OF CHATTANOOGA SHALE
DOE Office of Scientific and Technical Information (OSTI.GOV)
Bates, T.F.; Strahl, E.O.
1957-01-01
Qualitative and quantitative mineralogical studies of the Chattanooga Shale are in progress. Problems of separation and analysis of mineral and organic components are difficult because the rock is fine-grained. However, the applicaiion of light and electron microscopy, x-ray diffraction, nuclear-track study, and other methods has provided data of interest. Megascopically, the shalc is a massive chocolate-brown sediment which displays faint indications of lamination. Some pyrite lenses, nodules, and crystals and a few mica flakes are large enough to be seen with a hand lens. In thin section the rock is seen to consist of grains of quartz and feldspar inmore » a matrix of yellow to red--brown organic material, which incorporates shreds of mica and probably clay particles and is dotted by small clusters of pyrite. Larger organic fragments with associated pyrite are common and take various forms. Individual mineral particles range from pyrite cubes less than 0.15 micron on a side to quartz and feldspar grains as large as 0.10 mm. X-ray studies show the clay minerals to be illite, kaolinite, and chlorite in decreasing order of abundance. Tourmaline, zircon, and apatite are the characteristic heavy minerals of the sediment. Quantitative studies, accomplished by a combination of chemical and mineralogical methods, have shown the composition of a batch sample of this rock to be approxiinately: 22% quartz, 9% feldspar, 31% illite and kaolinite, 22% organic matter, 11% pyrite and marcasite, 2% chlorite, 2% iron oxides, and l% tourmaline, zircon, and apatite. Alphatrack studies of cniulsion-covered thin sections indicate that no uranium mineral is present. Approximately 70% of the uranium atoms is randomly distributed throughout the finegrained matrix of the rock, whereas another 25% is concentrated in organic-pyrite-clay complexes such as pyrite nodules and discrete organic bodies. In unweathered samples there is no relationship between uranium distribution and textural fcatures such as bedding. The data indicate that the uranium was precipitated from sea water under reducing conditions and has not been redistributed following compaction of the sediment. (auth)« less
Leo, Gerhard W.; Pavich, M.J.; Obermeier, Stephen F.
1977-01-01
Undisturbed cores of saprolite developed on crystalline rocks of the Piedmont Province in Fairfax County, Virginia have been obtained using a combination of Shelby tubes, Denison sampler, and modified diamond core-drilling. The principal purpose of the core study is to correlate variations in chemistry, mineralogy and texture with engineering properties throughout the weathering profile. Coring sites were chosen to obtain a maximum depth of weathering on diverse lithologies. The rocks investigated include pelitic schist, metagraywacke, granite, diabase and serpentinite. Four to twelve samples per core were selected, depending on thickness of 1) the weathering profile (from about 1 m in serpentinite to more than 30 m in pelitic schist) and on 2) megascopic changes in saprolite character for analysis of petrography, texture, clay mineralogy andd major element chemistry. Shear strength and compressibility were determined on corresponding segments of core. Standard penetration tests were performed adjacent to coring sites to evaluate engineering properties in situ. Geochemical changes of saprolite developed from each rock type follow predictable trends from fresh rock to soil profile, with relative Increases in Si, Ti, Al, Fe3+ and H20; variable K; and relative loss of Fe 2+, Mg, Ca, and Na. These variations are more pronounced in the weathering profiles over mafic and ultramafic rocks than metagraywacke. Clay minerals in granite, schist and metagraywacke saprolite are kaolinite, dioctahedral vermiculite, interlayered micavermiculite, and minor illite. Gibbsite is locally developed in near-surface samples of schist. Standard penetration test data for the upper 7 m of saprolite over schist and metagraywacke suggest alternations between stronger and weaker horizons than probably reflect variations in lithology including the presence of quartz lenses. Results for granite saprolite are most consistent but indicate lower strength. Shear strength increases fairly regularly downward in the weathering profile. The engineering behavior of diabase saprolite is controlled by a dense, plastic, near-surface clay layer (montmorillonite and kaolinite)overlying rock which is weathered to a granular state (grus), while engineering properties of serpentinite are determined by a very thin weathering profile.
NASA Astrophysics Data System (ADS)
Yoshioka, Mayumi; Takakura, Shinichi; Uchida, Youhei
2018-05-01
To estimate the groundwater flow around a borehole heat exchanger (BHE), thermal properties of geological core samples were measured and a thermal response test (TRT) was performed in the Tsukuba upland, Japan. The thermal properties were measured at 57 points along a 50-m-long geological core, consisting predominantly of sand, silt, and clay, drilled near the BHE. In this TRT, the vertical temperature in the BHE was also monitored during and after the test. Results for the thermal properties of the core samples and from the monitoring indicated that groundwater flow enhanced thermal transfers, especially at shallow depths. The groundwater velocities around the BHE were estimated using a two-dimensional numerical model with monitoring data on temperature changes. According to the results, the estimated groundwater velocity was generally consistent with hydrogeological data from previous studies, except for the data collected at shallow depths consisting of a clay layer. The reasons for this discrepancy at shallow depths were predicted to be preferential flow and the occurrence of vertical flow through the BHE grout, induced by the hydrogeological conditions.
Reactivity of clay minerals with acids and alkalies
Carroll, Dorothy; Starkey, Harry C.
1971-01-01
One-g samples of a montmorillonite, a metabentonite, an illite, two kaolinites, and three halloysites were treated with 50 ml of hydrochloric acid (6⋅45 N, 1:1), acetic acid (4⋅5 N, 1:3), sodium hydroxide (2⋅8 N), sodium chloride solution (pH 6⋅10; Na = 35‰; Cl = 21⋅5‰), and natural sea water (pH 7⋅85; Na = 35⋅5‰; Cl = 21⋅ 5‰) for a 10-day period in stoppered plastic vials. The supernatant solutions were removed from the clay minerals and analyzed for SiO2, Al2O3, CaO, MgO, Na2O, and K2O. All the solutions removed some SiO2, Al2O3, and Fe2O3 from the samples, but the quantities were small. Sodium hydroxide attacked the kaolin group minerals more strongly than it did montmorillonite, metabentonite, or illite. Halloysite was more strongly attacked by hydrochloric acid than was any of the other experimental minerals. Hydrochloric acid removed iron oxide coatings from soil clay minerals, but acetic acid did not remove them completely. The samples most strongly attacked by HCl and NaOH were examined by X-ray diffraction. Acid treatment did not destroy the structure of the clays, but the halloysite structure was partially destroyed. Sodium hydroxide attacked the halloysite structure, as shown by chemical analysis and X-ray diffraction. These experiments show that treatment in dilute acids has no harmful effect in the preparation of clays for X-ray diffraction. Acetic acid is preferred to hydrochloric acid for this purpose. Hydrochloric acid cleans clay minerals by removing free iron oxide from the surface; acetic acid is less effective.
Depositional and diagenetic processes of Qa Khanna playa, North Jordan basaltic plateau, Jordan
NASA Astrophysics Data System (ADS)
Howari, F. M.; Banat, K. M.; Abu-Salha, Y. A.
2010-09-01
The present study explored mineral occurrences and sediment characteristics of playas from northern Jordan and explained depositional and diagenetic processes as reflected from bulk chemistry and sedimentary structures. Mudcracks of different sizes and shape patterns, laminations, intersediment vesicles, and bioturbation pipes are the main sedimentary structures. Plagioclase, olivine, orthopyroxene, nepheline and other opaque minerals are all of detrital origin, and are derived from the basaltic bedrocks surrounding the studied playa. Evaporites are very rare; they are represented only by trace amounts of gypsum. The identified clay minerals in the clay fraction of the studied sediments, arranged according to their decreasing abundances are palygorskite, illite, kaolinite, smectite and chlorite. The elemental abundances were tied to clay, CaCO 3 and nearby igneous rocks. The type of clay minerals, the high pH values of the studied sediments, and the considerable incorporation of Mg and K in palygorskite and illite respectively, may strongly reflect a high evaporative and alkaline environment under arid to semi-arid conditions in an ephemeral lake of the Qa Khanna. Concentrations and distributions of both major and trace elements are essentially controlled by the clay mineralogy and the calcium carbonate content; Ca is mainly incorporated in the CaCO 3, which is either generated authigenically or by aeolian deposition. Fe and K are incorporated and fixed by illite under an evaporative and alkaline environment. Mg is incorporated in palygorskite while Mn is adsorbed on various clay minerals. Sr substitutes for Ca in the aeolian CaCO 3 and its presence in the studied sediments is independent of the prevailing conditions during the playa evolution. Rb substitutes for K in illite under the prevailing chemical conditions in the studied playa.
NASA Astrophysics Data System (ADS)
Elliott, W. C.; Lim, D.; Zaunbrecher, L. K.; Pickering, R. A.; Williams, K. H.; Navarre-Sitchler, A.; Long, P. E.; Noel, V.; Bargar, J.; Qafoku, N. P.
2015-12-01
Alluvial sediments deposited along the Colorado River corridor in the semi-arid regions of central to western Colorado can be important hosts for legacy contamination including U, V, As and Se. These alluvial sediments host aquifers which are thought to provide important "hot spots" and "hot moments" for microbiological activity controlling organic carbon processing and fluxes in the subsurface. Relatively little is known about the clay mineralogy of these alluvial aquifers and the parent alluvial sediments in spite of the fact that they commonly include lenses of silt-clay materials. These lenses are typically more reduced than coarser grained materials, but zones of reduced and more oxidized materials are present in these alluvial aquifer sediments. The clay mineralogy of the non-reduced parent alluvial sediments of the alluvial aquifer located in Rifle, CO (USA) is composed of chlorite, smectite, illite, kaolinite and quartz. The clay mineralogy of non-reduced fine-grained materials at Rifle are composed of the same suite of minerals found in the sediments plus a vermiculite-smectite intergrade that occurs near the bottom of the aquifer near the top of the Wasatch Formation. The clay mineral assemblages of the system reflect the mineralogically immature character of the source sediments. These assemblages are consistent with sediments and soils that formed in a moderately low rainfall climate and suggestive of minimal transport of the alluvial sediments from their source areas. Chlorite, smectite, smectite-vermiculite intergrade, and illite are the likely phases involved in the sorption of organic carbon and related microbial redox transformations of metals in these sediments. Both the occurrence and abundance of chlorite, smectite-vermiculite, illite and smectite can therefore exert an important control on the contaminant fluxes and are important determinants of biogeofacies in mountainous, semiarid terrains.
Johnson, W.H.
1971-02-02
A method is described for constructing a lined underground cavity. The process includes the steps of securing a casing in a borehole by grouting, underreaming the casing, filling the underreamed region with additional grouting, and then drilling through and underreaming the added grouting, thereby forming a room having a lining formed of the grouting. By using a structurally strong grouting that is impervious to water, the resulting room is waterproof and is suitable for on-site storage of an atomic device and its associated equipment prior to an underground atomic event. Such cavities also have other uses; for example, the cavities may be made very deep and used for storage of various fluids such as natural gas storage. (5 claims)
Test plan for formulation and evaluation of grouted waste forms with shine process wastes
DOE Office of Scientific and Technical Information (OSTI.GOV)
Ebert, W. L.; Jerden, J. L.
2015-09-01
The objective of this experimental project is to demonstrate that waste streams generated during the production of Mo99 by the SHINE Medical Technologies (SHINE) process can be immobilized in cement-based grouted waste forms having physical, chemical, and radiological stabilities that meet regulatory requirements for handling, storage, transport, and disposal.
NASA Astrophysics Data System (ADS)
Mohammadi, O.; Wehunt, K.; Chumpitaz, G. A.; Bravo, B.; Ruiz, J.; Dhesi, H.; Halling, M. C.; Pyles, C. G.; Guo, J.; Negrini, R. M.
2016-12-01
Tulare Lake, located in the southern San Joaquin Valley, California has been the site of repeated geologic and paleoclimate studies due to its well preserved sedimentary record based on core, trench exposures, and the mapping of geomorphic features. Yet, no studies have focused on the effect of depositional environment variations on mineralogy. In this study, a series of integrated geochemical, sedimentary, and grain-size climate proxy data from core TL05-4A encompassing the last 25 cal. ka BP were analyzed. Preliminary sedimentary results as determined by X-ray diffraction (XRD) reveal a clay-dominant mineral assemblage containing variable smectite, illite, kaolinite, and chlorite followed by a secondary non-clay contribution in the form of quartz, feldspar, and calcite. The relative abundance of these minerals varies with depth and is tied to regional shifts in climate as best exemplified by an observed rapid increase in bulk clay percentages (+50%) after the Tioga deglaciation event ( 14 cal. ka BP). Six climosequences were determined—three wet periods interspaced by three dry episodes over the last 25 ka. Two important dry periods characterized by gypsum and bassanite occurred from 10.7-9.4 cal. ka BP (Preboreal warming) and 8.2-5.2 cal. ka BP (Holocene Climate Optimum) indicating oxygen depletion, more intense evaporation, and reducing conditions in the lake. These abrupt dry phases may help explain the geographic range reduction and extirpation of Mammuthus primigenius and other North American megafanua as warmer and dryer regional conditions led to enhanced water stress and diminished net primary productivity.
Dimensional Stability of Grout-like Materials Used in Field-Cast Connections
DOT National Transportation Integrated Search
2016-12-01
The wide use of grouts and grout-like materials in the construction industry is seen in applications such as joint sealing, structural repair, and connections in prefabricated bridge elements (PBEs). Currently, different types of grouts are available...
2014-01-01
We have studied the impact of dissolved aluminum on interfacial properties of two aluminum bearing minerals, corundum and kaolinite. The effect of intentionally adding dissolved aluminum on electrokinetic potential of basal plane surfaces of sapphire was studied by streaming potential measurements as a function of pH and was complemented by a second harmonic generation (SHG) study at pH 6. The electrokinetic data show a similar trend as the SHG data, suggesting that the SHG electric field correlates to zeta-potential. A comparable study was carried out on kaolinite particles. In this case electrophoretic mobility was measured as a function of pH. In both systems the addition of dissolved aluminum caused significant changes in the charging behavior. The isoelectric point consistently shifted to higher pH values, the extent of the shift depending on the amount of aluminum present or added. The experimental results imply that published isoelectric points of clay minerals may have been affected by this phenomenon. The presence of dissolved aluminum in experimental studies may be caused by particular pre-treatment methods (such as washing in acids and subsequent adsorption of dissolved aluminum) or even simply by starting a series of measurements from extreme pH (causing dissolution), and subsequently varying the pH in the very same batch. This results in interactions of dissolved aluminum with the target surface. A possible interpretation of the experimental results could be that at low aluminum concentrations adatoms of aluminum (we will refer to adsorbed mineral constituents as adatoms) can form at the sapphire basal plane, which can be rather easily removed. Simultaneously, once the surface has been exposed to sufficiently high aluminum concentration, a visible change of the surface is seen by AFM which is attributed to a surface precipitate that cannot be removed under the conditions employed in the current study. In conclusion, whenever pre-treatment or the starting point of an experiment favor the dissolution of aluminum, dissolved Al may remain in the experimental system and interact with the target surfaces. The systems are then no longer pristine and points of zero charge or sorption data are those of aluminum-bearing systems. PMID:25045321
NASA Astrophysics Data System (ADS)
Bougeault, Cédric; Pellenard, Pierre; Deconinck, Jean-François; Hesselbo, Stephen P.; Dommergues, Jean-Louis; Bruneau, Ludovic; Cocquerez, Théophile; Laffont, Rémi; Huret, Emilia; Thibault, Nicolas
2017-02-01
The Early Jurassic was broadly a greenhouse climate period that was punctuated by short warm and cold climatic events, positive and negative excursions of carbon isotopes, and episodes of enhanced organic matter burial. Clay minerals from Pliensbachian sediments recovered from two boreholes in the Paris Basin, are used here as proxies of detrital supplies, runoff conditions, and palaeoceanographic changes. The combined use of these minerals with stable isotope data (C-O) from bulk carbonates and organic matter allows palaeoclimatic reconstructions to be refined for the Pliensbachian. Kaolinite/illite ratio is discussed as a reliable proxy of the hydrological cycle and runoff from landmasses. Three periods of enhanced runoff are recognised within the Pliensbachian. The first one at the Sinemurian-Pliensbachian transition shows a significant increase of kaolinite concomitant with the negative carbon isotope excursion at the so-called Sinemurian Pliensbachian Boundary Event (SPBE). The Early/Late Pliensbachian transition was also characterised by more humid conditions. This warm interval is associated with a major change in oceanic circulation during the Davoei Zone, likely triggered by sea-level rise; the newly created palaeogeography, notably the flooding of the London-Brabant Massif, allowed boreal detrital supplies, including kaolinite and chlorite, to be exported to the Paris Basin. The last event of enhanced runoff occurred during the late Pliensbachian (Subnodosus Subzone of the Margaritatus Zone), which occurred also during a warm period, favouring organic matter production and preservation. Our study highlights the major role of the London Brabant Massif in influencing oceanic circulation of the NW European area, as a topographic barrier (emerged lands) during periods of lowstand sea-level and its flooding during period of high sea-level. This massif was the unique source of smectite in the Paris Basin. Two episodes of smectite-rich sedimentation ('smectite events'), coincide with regressive intervals, indicating emersion of the London Brabant Massif and thus suggesting that an amplitude of sea-level change high enough to be linked to glacio-eustasy. This mechanism is consistent with sedimentological and geochemical evidences of continental ice growth notably during the Latest Pliensbachian (Spinatum Zone), and possibly during the Early Pliensbachian (late Jamesoni/early Ibex Zones).
A portable high-power diode laser-based single-stage ceramic tile grout sealing system
NASA Astrophysics Data System (ADS)
Lawrence, J.; Schmidt, M. J. J.; Li, L.; Edwards, R. E.; Gale, A. W.
2002-02-01
By means of a 60 W high-power diode laser (HPDL) and a specially developed grout material the void between adjoining ceramic tiles has been successfully sealed. A single-stage process has been developed which uses a crushed ceramic tile mix to act as a tough, inexpensive bulk substrate and a glazed enamel surface to provide an impervious surface glaze. The single-stage ceramic tile grout sealing process yielded seals produced in normal atmospheric conditions that displayed no discernible cracks and porosities. The single-stage grout is simple to formulate and easy to apply. Tiles were successfully sealed with power densities as low as 200 kW/ mm2 and at rates of up to 600 mm/ min. Bonding of the enamel to the crushed ceramic tile mix was identified as being primarily due to van der Waals forces and, on a very small scale, some of the crushed ceramic tile mix material dissolving into the glaze. In terms of mechanical, physical and chemical characteristics, the single-stage ceramic tile grout was found to be far superior to the conventional epoxy tile grout and, in many instances, matched and occasionally surpassed that of the ceramic tiles themselves. What is more, the development of a hand-held HPDL beam delivery unit and the related procedures necessary to lead to the commercialisation of the single-stage ceramic tile grout sealing process are presented. Further, an appraisal of the potential hazards associated with the use of the HPDL in an industrial environment and the solutions implemented to ensure that the system complies with the relevant safety standards are given.
NASA Astrophysics Data System (ADS)
Xie, Xiongyao; Liu, Yujian; Huang, Hongwei; Du, Jun; Zhang, Fengshou; Liu, Lanbo
2007-09-01
For shield tunnelling construction in soft soil areas, the coverage uniformity and quality of consolidation of the injected grout mortar behind the prefabricated tunnel segment is the main concern for tunnel safety and ground settlement. In this paper, ground-penetrating radar (GPR) was applied to evaluate the grout behind the tunnel lining segments in Shanghai, China. The dielectric permittivity of the grout material in Shanghai Metro tunnelling construction was measured in the laboratory. Combining physical modelling results with finite different time domain numerical modelling results, we suggest that the antenna with frequency 200 MHz is well suited to penetrate the reinforced steel bar network of the tunnel lining segment and testing grout patterns behind the segment. The electromagnetic velocity of the grout behind the segment of the tunnel is 0.1 m ns-1 by the analysis of field common-middle point data. A wave-translated method was put forward to process the GPR images. Furthermore, combining the information acquired by GPR with experience data, a GPR non-destructive test standard for the grout mortar evaluation in Shanghai Metro tunnel construction was brought forward. The grout behind the tunnel lining segment is classified into three types: uncompensated grout mortar with a thickness less than 10 cm, normal grout mortar with a thickness between 10 cm and 30 cm and overcompensated grout mortar, which is more than 30 cm thick. The classified method is easily put into practice.
Stochastic Approach to Determine CO2 Hydrate Induction Time in Clay Mineral Suspensions
NASA Astrophysics Data System (ADS)
Lee, K.; Lee, S.; Lee, W.
2008-12-01
A large number of induction time data for carbon dioxide hydrate formation were obtained from a batch reactor consisting of four independent reaction cells. Using resistance temperature detector(RTD)s and a digital microscope, we successfully monitored the whole process of hydrate formation (i.e., nucleation and crystal growth) and detected the induction time. The experiments were carried out in kaolinite and montmorillonite suspensions at temperatures between 274 and 277 K and pressures ranging from 3.0 to 4.0 MPa. Each set of data was analyzed beforehand whether to be treated by stochastic manner or not. Geochemical factors potentially influencing the hydrate induction time under different experimental conditions were investigated by stochastic analyses. We observed that clay mineral type, pressure, and temperature significantly affect the stochastic behavior of the induction times for CO2 hydrate formation in this study. The hydrate formation kinetics along with stochastic analyses can provide basic understanding for CO2 hydrate storage in deep-sea sediment and geologic formation, securing its stability under the environments.
NASA Astrophysics Data System (ADS)
Yan, X. Q.; Zhou, C. Y.; Fang, Y. G.; Lin, L. S.
2017-12-01
The specific surface area (SSA) has a great influence on the physical and chemical properties of fine-grained soils. Determination of specific surface area is an important content for fine-grained soils micro-meso analysis and characteristic research. In this paper, mercury intrusion porosimetry (MIP) was adopted to determine the SSA of fine-grained soils including quartz, kaolinite, bentonite and natural Shenzhen soft clay. The test results show that the average values of SSA obtained by MIP are 0.78m2/g, 11.31m2/g, 57.28m2/g and 27.15m2/g respectively for very fine-grained quartz, kaolin, bentonite and natural Shenzhen soft clay, and that it is feasible to apply MIP to obtain the SSA of fine-grained soils through statistical analysis of 97 samples. Through discussion, it is necessary to consider the state of fine-grained soils such as pore ratio when the SSA of fine-grained soils is determined by MIP.
Thermal expansion of ceramic samples containing natural zeolite
NASA Astrophysics Data System (ADS)
Sunitrová, Ivana; Trník, Anton
2017-07-01
In this study the thermal expansion of ceramic samples made from natural zeolite is investigated. Samples are prepared from the two most commonly used materials in ceramic industry (kaolin and illite). The first material is Sedlec kaolin from Czech Republic, which contains more than 90 mass% of mineral kaolinite. The second one is an illitic clay from Tokaj area in Hungary, which contains about 80 mass% of mineral illite. Varying amount of the clay (0 % - 50 %) by a natural zeolite from Nižný Hrabovec (Slovak Republic), containing clinoptilolite as major mineral phase is replaced. The measurements are performed on cylindrical samples with a diameter 14 mm and a length about 35 mm by a horizontal push - rod dilatometer. Samples made from pure kaolin, illite and zeolite are also subjected to this analysis. The temperature regime consists from linear heating rate of 5 °C/min from 30 °C to 1100 °C. The results show that the relative shrinkage of ceramic samples increases with amount of zeolite in samples.
Mineralogical variation in the size fractions of a Ranong kaolin, southern Thailand
NASA Astrophysics Data System (ADS)
Pisutha-Arnond, Visut; Phuvichit, Suraphol; Leepowpanth, Quanchai
A representative crude Ranong kaolin from the Thungkla-Ranong mine was separated into > 2 mm (granule), 2-1 mm (very coarse sand), 1-0.5 mm (coarse sand), 0.5-0.25 mm (medium sand), 0.25-0.125 mm (fine sand), 0.125-0.062 mm (very fine sand) and 62-28, 28-14, 17-7, 7-4, 4-2, 2-1 and < 1 μ m size fractions. Those size fractions were analyzed by X-ray powder diffractometry (XRD), differential thermal analysis (DTA), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) with attached energy dispersive X-ray spectrometer (EDX). Kaolin group minerals were differentiated by using XRD in combination with various chemical and heat treatments together with TEM, SEM and DTA. The Ranong kaolin consists predominantly of tubular halloysite, poorly crystallized kaolinite and quartz with minor amounts of mica and K-feldspars. Other trace constituents include gibbsite, tourmaline, zircon and colored impurities (i.e. extractable iron hydroxide coating on clay mineral surface). The kaolin minerals are found in all size fractions by which their contents and halloysite/kaolinite ratios increase as the particle sizes become finer. Quartz and mica are also detected in almost all size fractions. They are, however, more abundant with coarsening particle size. Gibbsite, K-feldspar and tourmaline are mainly concentrated in the fine sand to silt size fractions. Crystallinity of kaolin minerals as measured by XRD varied moderately with size. Relatively pure kaolin minerals, predominantly halloysite and kaolinite, can be obtained in the particle size below 1 or 2 μm.
Dai, S.; Chou, C.-L.
2007-01-01
The minerals found in the no.5 coal (Late Permian) from the Zhaotong Coalfield, Yunnan Province, southwestern China, have been examined and found to consist mainly of kaolinite, pyrite, chamosite, quartz, and calcite, with trace amounts of illite and mixed-layer illite-smectite. The proportion of chamosite in clay minerals ranges from 32 to 56 wt%, with an average of 46 wt%. Chamosite is distributed not only in collodetrinite, but also occurs as cell fillings in fusinite, semifusinite, and telinite. The high content and mode of occurrence of chamosite in this mine indicate its formation by interaction of kaolinite with Fe-Mg-rich fluids during early diagenesis. Except for a minor amount of terfigenous quartz, most quartz is of authigenic origin and formed from kaolinite desilication. The calcite content of the no. 5 coal is 1.4-6.3% (with an average of 3%) and is distributed in collodetrinite and as cell fillings of coal-forming plants. Calcite originated from seawater invasion during peat accumulation. Pyrite occurs in several ways: as massive, framboidal, isolated enhedral/ anhedral, and euhedral forms. In addition, the presence of a large amount of pyritized red algae provides strong evidence of seawater invasion during peat accumulation. The red algae may have played an important role in the enrichment of sulfur in the coal. The characteristic assemblage of minerals in this mine resulted from a unique basinal environment in which the mineral matter was derived from a basaltic source region, volcanic activity, and seawater transgression during coal formation.
Greathouse, J. A.; Cygan, R. T.; Fredrich, J. T.; ...
2017-09-28
Molecular simulations of the adsorption of representative organic molecules onto the basal surfaces of various clay minerals were used to assess the mechanisms of enhanced oil recovery associated with salinity changes and water flooding. Simulations at the density functional theory (DFT) and classical levels provide insights into the molecular structure, binding energy, and interfacial behavior of saturate, aromatic, and resin molecules near clay mineral surfaces. Periodic DFT calculations reveal binding geometries and ion pairing mechanisms at mineral surfaces while also providing a basis for validating the classical force field approach. Through classical molecular dynamics simulations, the influence of aqueous cationsmore » at the interface and the role of water solvation are examined to better evaluate the dynamical nature of cation-organic complexes and their co-adsorption onto the clay surfaces. The extent of adsorption is controlled by the hydrophilic nature and layer charge of the clay mineral. All organic species studied showed preferential adsorption on hydrophobic mineral surfaces. However, the anionic form of the resin (decahydro-2-naphthoic acid)—expected to be prevalent at near-neutral pH conditions in petroleum reservoirs—readily adsorbs to the hydrophilic kaolinite surface through a combination of cation pairing and hydrogen bonding with surface hydroxyl groups. Analysis of cation-organic pairing in both the adsorbed and desorbed states reveals a strong preference for organic anions to coordinate with divalent calcium ions rather than monovalent sodium ions, lending support to current theories regarding low-salinity water flooding.« less
DOE Office of Scientific and Technical Information (OSTI.GOV)
Greathouse, J. A.; Cygan, R. T.; Fredrich, J. T.
Molecular simulations of the adsorption of representative organic molecules onto the basal surfaces of various clay minerals were used to assess the mechanisms of enhanced oil recovery associated with salinity changes and water flooding. Simulations at the density functional theory (DFT) and classical levels provide insights into the molecular structure, binding energy, and interfacial behavior of saturate, aromatic, and resin molecules near clay mineral surfaces. Periodic DFT calculations reveal binding geometries and ion pairing mechanisms at mineral surfaces while also providing a basis for validating the classical force field approach. Through classical molecular dynamics simulations, the influence of aqueous cationsmore » at the interface and the role of water solvation are examined to better evaluate the dynamical nature of cation-organic complexes and their co-adsorption onto the clay surfaces. The extent of adsorption is controlled by the hydrophilic nature and layer charge of the clay mineral. All organic species studied showed preferential adsorption on hydrophobic mineral surfaces. However, the anionic form of the resin (decahydro-2-naphthoic acid)—expected to be prevalent at near-neutral pH conditions in petroleum reservoirs—readily adsorbs to the hydrophilic kaolinite surface through a combination of cation pairing and hydrogen bonding with surface hydroxyl groups. Analysis of cation-organic pairing in both the adsorbed and desorbed states reveals a strong preference for organic anions to coordinate with divalent calcium ions rather than monovalent sodium ions, lending support to current theories regarding low-salinity water flooding.« less
De la Varga, I; Muñoz, J F; Bentz, D P; Spragg, R P; Stutzman, P E; Graybeal, B A
2018-05-01
Bond between two cementitious materials is crucial in applications such as repairs, overlays, and connections of prefabricated bridge elements (PBEs), to name just a few. It is the latter that has special interest to the authors of this paper. After performing a dimensional stability study on grout-like materials commonly used as connections between PBEs, it was observed that the so-called 'non-shrink' cementitious grouts showed a considerable amount of early-age shrinkage. This might have negative effects on the integrity of the structure, due not only to the grout material's early degradation, but also to a possible loss of bond between the grout and the prefabricated concrete element. Many factors affect the bond strength between two cementitious materials (e.g., grout-concrete), the presence of moisture at the existing concrete substrate surface being one of them. In this regard, pre-moistening the concrete substrate surface prior to the application of the grout material is sometimes recommended for bond enhancement. This topic has been the focus of numerous research studies in the past; however, there is still controversy among practitioners on the real benefits that this practice might provide. This paper evaluates the tensile bond performance of two non-shrink cementitious grouts applied to the exposed aggregate surface of a concrete substrate, and how the supply of moisture at the grout-concrete interface affects the bond strength. "Pull-off" bond results show increased tensile bond strength when the concrete surface is pre-moistened. Reasons to explain the observed increased bond strength are given after a careful microstructural analysis of the grout-concrete interface. Interfaces where sufficient moisture is provided to the concrete substrate such that moisture movement from the grout is prevented show reduced porosity and increased hydration on the grout side of the interface, which is thought to directly contribute to the increased tensile bond strength.
Methods and system for subsurface stabilization using jet grouting
Loomis, Guy G.; Weidner, Jerry R.; Farnsworth, Richard K.; Gardner, Bradley M.; Jessmore, James J.
1999-01-01
Methods and systems are provided for stabilizing a subsurface area such as a buried waste pit for either long term storage, or interim storage and retrieval. A plurality of holes are drilled into the subsurface area with a high pressure drilling system provided with a drill stem having jet grouting nozzles. A grouting material is injected at high pressure through the jet grouting nozzles into a formed hole while the drill stem is withdrawn from the hole at a predetermined rate of rotation and translation. A grout-filled column is thereby formed with minimal grout returns, which when overlapped with other adjacent grout-filled columns encapsulates and binds the entire waste pit area to form a subsurface agglomeration or monolith of grout, soil, and waste. The formed monolith stabilizes the buried waste site against subsidence while simultaneously providing a barrier against contaminate migration. The stabilized monolith can be left permanently in place or can be retrieved if desired by using appropriate excavation equipment. The jet grouting technique can also be utilized in a pretreatment approach prior to in situ vitrification of a buried waste site. The waste encapsulation methods and systems are applicable to buried waste materials such as mixed waste, hazardous waste, or radioactive waste.
Epoxy Grout With Silica Thickener
NASA Technical Reports Server (NTRS)
Mcclung, C. E.
1984-01-01
Grout cures quickly, even in presence of hydraulic oil. Grout is mixture of aggregate particles, finely-divided silica, epoxy resin, and triethylenetetramine curing agent, with mixture containing about 85 percent silica and aggregate particle sand 15 percent resin and curing agent. Silica is thickening agent and keeps grout from sagging.
NASA Astrophysics Data System (ADS)
Akin, Muge K.
2016-04-01
The term of ground improvement states to the modification of the engineering properties of soils. Jet-grouting is one of the grouting methods among various ground improvement techniques. During jet-grouting, different textures of columns can be obtained depending on the characteristics of surrounding subsoil as well as the adopted jet-grouting system for each site is variable. In addition to textural properties, strength and index parameters of jet-grout columns are highly affected by the adjacent soil. In this study, the physical and mechanical properties of jet-grout columns constructed at two different sites in silty and sandy soil conditions were determined by laboratory tests. A number of statistical relationships between physical and mechanical properties of soilcrete were established in this study in order to investigate the dependency of numerous variables. The relationship between qu and γd is more reliable for sandy soilcrete than that of silty columns considering the determination coefficients. Positive linear relationships between Vp and γd with significantly high determination coefficients were obtained for the jet-grout columns in silt and sand. The regression analyses indicate that the P-wave velocity is a very dominant parameter for the estimation of physical and mechanical properties of jet-grout columns and should be involved during the quality control of soilcrete material despite the intensive use of uniaxial compressive strength test. Besides, it is concluded that the dry unit weight of jet-grout column is a good indicator of the efficiency of employed operational parameters during jet-grouting.
NASA Astrophysics Data System (ADS)
Quille, Rubén; Bustamante, Ángel; Palomino, Ybar
2011-11-01
The ceramic industry is an important area of economic activity in the Ayacucho Region, in particular in the District of Quinua. As a consequence, there is a huge demand for clay to produce ceramic pastes in that region. This paper reports on results concerning the mineralogical characterization of four clayey samples, which were collected MAA and SPQA from the area Pampa de La Quinua with geographic coordinates 13° 02' 49″ S 74° 08' 03″ W, CE1M and CE2M from the Quinua locality 13° 03' 07″ S 74° 08' 31″ W, both in the District of Quinua, Province of Huamanga, Ayacucho, Peru. The chemical and mineralogical characterization of these samples was carried out with powder X-ray diffraction detecting quartz, albite, montmorillonite, kaolinite and glauconite mineral phases, Mössbauer spectroscopy detected iron in kaolinite, glauconite and montmorillonite minerals. Chemical analysis was performed through scanning electron microscopy and energy dispersive X-ray spectroscopy. Data obtained from the combination of these techniques provided relevant information about the morphology, chemical composition, and the mineralogy of samples.
Cheng, Hongfei; Yang, Jing; Liu, Qinfu; Zhang, Jinshan; Frost, Ray L
2010-11-01
Mid-infrared (MIR) and near-infrared (NIR) spectroscopy have been compared and evaluated for differentiating kaolinite, coal bearing kaolinite and halloysite. Kaolinite, coal bearing kaolinite and halloysite are the three relative abundant minerals of the kaolin group, especially in China. In the MIR spectra, the differences are shown in the 3000-3600 cm⁻¹ between kaolinite and halloysite. It cannot obviously differentiate the kaolinite and halloysite, leaving alone kaolinite and coal bearing kaolinite. However, NIR, together with MIR, gives us the sufficient evidence to differentiate the kaolinite and halloysite, especially kaolinite and coal bearing kaolinite. There are obvious differences between kaolinite and halloysite in all range of their spectra, and they also show some difference between kaolinite and coal bearing kaolinite. Therefore, the reproducibility of measurement, signal to noise ratio and richness of qualitative information should be simultaneously considered for proper selection of a spectroscopic method for mineral analysis. Copyright © 2010 Elsevier B.V. All rights reserved.
Chen, Chunmei; Dynes, James J; Wang, Jian; Karunakaran, Chithra; Sparks, Donald L
2014-06-17
There is a growing acceptance that associations with soil minerals may be the most important overarching stabilization mechanism for soil organic matter. However, direct investigation of organo-mineral associations has been hampered by a lack of methods that can simultaneously characterize organic matter (OM) and soil minerals. In this study, STXM-NEXAFS spectroscopy at the C 1s, Ca 2p, Fe 2p, Al 1s, and Si 1s edges was used to investigate C associations with Ca, Fe, Al, and Si species in soil clay fractions from an upland pasture hillslope. Bulk techniques including C and N NEXAFS, Fe K-edge EXAFS spectroscopy, and XRD were applied to provide additional information. Results demonstrated that C was associated with Ca, Fe, Al, and Si with no separate phase in soil clay particles. In soil clay particles, the pervasive C forms were aromatic C, carboxyl C, and polysaccharides with the relative abundance of carboxyl C and polysaccharides varying spatially at the submicrometer scale. Only limited regions in the soil clay particles had aliphatic C. Good C-Ca spatial correlations were found for soil clay particles with no CaCO3, suggesting a strong role of Ca in organo-mineral assemblage formation. Fe EXAFS showed that about 50% of the total Fe in soils was contained in Fe oxides, whereas Fe-bearing aluminosilicates (vermiculite and Illite) accounted for another 50%. Fe oxides in the soil were mainly crystalline goethite and hematite, with lesser amounts of poorly crystalline ferrihydrite. XRD revealed that soil clay aluminosilicates were hydroxy-interlayered vermiculite, Illite, and kaolinite. C showed similar correlation with Fe to Al and Si, implying a similar association of Fe oxides and aluminosilicates with organic matter in organo-mineral associations. These direct microscopic determinations can help improve understanding of organo-mineral interactions in soils.
NASA Astrophysics Data System (ADS)
Lee, J.; Khim, B. K.; Cho, H. G.; Kim, S.; 353 Scientists, I. E.
2016-12-01
Clay mineral studies in the Bengal Fan have allowed the reconstruction of the erosional history of the Himalayan-Tibetan complex since the Early Miocene. Several factors such as climate change and tectonic activity are important for the erosion rate of the Himalaya-Tibet complex. IODP Expedition 353 Site U1447 (10°47.4'N, 93°00'E; 1391 mbsl) was drilled on a ridge 45 km offshore Little Andaman Island in the Andaman Sea, penetrating to total depths of 738 m. Riverine sediments supplied mainly by the Irrawaddy and Salween (draining the Indo-Burman Ranges; smectite-rich) and the Ganga/Brahmaputra (draining the Himalaya; illite-rich) via the surface currents have been known to deposit in the Andaman Sea. We measured clay minerals of 38 sediment samples collected from 150 to 737 m CSF-A at Site U1447 in order to reveal long-term variation patterns of clay minerals and their controlling factors. Age reconstruction of Site U1447 aided by shipboard biostratigraphic and paleomagnetic data defined the study interval spanning from the Late Miocene ( 10 Ma) to Early Pleistocene ( 1.25 Ma). At this interval, clay minerals consist mainly of smectite (28-61% with an average of 47%) followed by illite (20-41% with an average of 29%), kaolinite (9-19% with an average of 14%), and chlorite (5-15% with an average of 10%). Variation of clay mineral compositions is divided into three stages; almost consistent variations of all clay minerals (from 750 to 570 m CSF-A; 10.0 to 7.5 Ma), gradual decrease of smectite and increase of illite and chlorite (from 570 to 400 m CSF-A; 7.5 to 4.5 Ma), and great fluctuation of all clay minerals (from 400 to 150 m CSF-A; 4.5 to 1.1 Ma). Such long-term clay mineral changes may be related to provenance switches, tectonic evolution of the source regions, climatic variations, degree of volcanism with basin evolution, sedimentation history by sea level changes or some combination of these factors.
Role of clay minerals in the formation of atmospheric aggregates of Saharan dust
NASA Astrophysics Data System (ADS)
Cuadros, Javier; Diaz-Hernandez, José L.; Sanchez-Navas, Antonio; Garcia-Casco, Antonio
2015-11-01
Saharan dust can travel long distances in different directions across the Atlantic and Europe, sometimes in episodes of high dust concentration. In recent years it has been discovered that Saharan dust aerosols can aggregate into large, approximately spherical particles of up to 100 μm generated within raindrops that then evaporate, so that the aggregate deposition takes place most times in dry conditions. These aerosol aggregates are an interesting phenomenon resulting from the interaction of mineral aerosols and atmospheric conditions. They have been termed "iberulites" due to their discovery and description from aerosol deposits in the Iberian Peninsula. Here, these aggregates are further investigated, in particular the role of the clay minerals in the aggregation process of aerosol particles. Iberulites, and common aerosol particles for reference, were studied from the following periods or single dust events and locations: June 1998 in Tenerife, Canary Islands; June 2001 to August 2002, Granada, Spain; 13-20 August 2012, Granada; and 1-6 June 2014, Granada. Their mineralogy, chemistry and texture were analysed using X-ray diffraction, electron microprobe analysis, SEM and TEM. The mineral composition and structure of the iberulites consists of quartz, carbonate and feldspar grains surrounded by a matrix of clay minerals (illite, smectite and kaolinite) that also surrounds the entire aggregate. Minor phases, also distributed homogenously within the iberulites, are sulfates and Fe oxides. Clays are apparently more abundant in the iberulites than in the total aerosol deposit, suggesting that iberulite formation concentrates clays. Details of the structure and composition of iberulites differ from descriptions of previous samples, which indicates dependence on dust sources and atmospheric conditions, possibly including anthropic activity. Iberulites are formed by coalescence of aerosol mineral particles captured by precursor water droplets. The concentration of clays in the iberulites is suggested to be the result of higher efficiency for clay capture than for the capture of larger mineral grains. The high hygroscopicity of clay minerals probably causes retention of water in the evaporation stage and some secondary minerals (mainly gypsum) are associated with clays.
Goure-Doubi, Herve; Martias, Céline; Lecomte-Nana, Gisèle Laure; Nait-Ali, Benoît; Smith, Agnès; Thune, Elsa; Villandier, Nicolas; Gloaguen, Vincent; Soubrand, Marilyne; Konan, Léon koffi
2014-11-15
The aim of this study was to understand the mechanisms responsible for the strengthening of "geomimetic" materials, especially the chemical bonding between clay and humic substances. The mineral matter is lateritic clay which mainly consists in kaolinite, goethite, hematite and quartz. The other starting products are fulvic acid (FA) and lime. The preparation of these geomimetic materials is inspired from the natural stabilization of soils by humic substances occurring over thousands of years. The present process involves acidic and alkaline reactions followed by a curing period of 18days at 60°C under a water saturated atmosphere. The acceleration of the strengthening process usually observed in soils makes this an original process for treatment of soils. The consolidation of the "geomimetic" materials could result from two major phenomena: (i) chemical bonding at the interface between the clay particles and iron compounds and the functional groups of the fulvic acid, (ii) a partial dissolution of the clay grains followed by the precipitation of the cementitious phases, namely calcium silicate hydrates, calcium aluminate hydrates and mixed calcium silicum and aluminum hydrates. Indeed, the decrease of the BET specific area of the lateritic clay after 24 h of reaction with FA added to the structural reorganization observed between 900 and 1000°C in the "geomimetic" material, and to the results of adsorption measurements, confirm the formation of organo-ferric complexes. The presence of iron oxides in clay, in the form of goethite, appears to be another parameter in favor of a ligand exchange process and the creation of binding bridges between FA and the mineral matter. Indeed all faces of goethite are likely to be involved in complexation reactions whereas in lateritic clay only lateral faces could be involved. The results of the adsorption experiments realized at a local scale will improve our understandings about the process of adsorption of FA on lateritic clays and its involvement in the strengthening process of materials. Copyright © 2014 Elsevier Inc. All rights reserved.
Brief overview of the various families of grouts and their aplications
DOE Office of Scientific and Technical Information (OSTI.GOV)
Nandts, A.
1989-04-01
It is difficult to maintain an up-to-date overview of all the grouts presently used on the international market. Better grouts are continuously developed and more formulators are making their appearance. Consequently, it is difficult to clearly define all of the products in the industry. This topic has been the subject of numerous papers and textbooks. Most authors, however, only focus on their fields of interest: applications in geotechnical, or rehabilitation, or seepage control in civil engineering, oil or mining industry. There has been a limited transfer of technology from one field to the other because of the enormous differences inmore » magnitude, site conditions and consequently the application techniques. The tools an engineer has are: his expertise in grouting and engineering background, equipment available or to be designed or modified to carry out a particular job, relevant data available from other sciences, and products with a variety of characteristics. This paper concentrates on product selection. The most suitable product for a particular project requires a good understanding of the general chemical and mechanical characteristics of the grout. The grouts have been classified into four categories for the purpose of this paper. There may be other methods of classification; however, this is only an attempt to help the industry with the selection of the most suitable grout for a given application. The four categories are: suspension grouts, chemical grouts, hot melts, and precipitation grouts. 1 fig.« less
Analysis of Causes of Uplift Anomalies in the Čierny Váh Subsoil
NASA Astrophysics Data System (ADS)
Bednárová, Emília; Grambličková, Danka; Škvarka, Juraj; Majerčák, Vlastimil; Slávik, Ivan
2017-12-01
The pumped storage hydropower plant of Čierny Váh was created by means of damming up the valley of the Čierny Váh River. The dam is 18.5 m high above terrain and 375 m long in the dam’s crest. Total capacity of the reservoir is 5.1 million m3. Complicated geological conditions in the subsoil of dam’s body - fractured dolomite with local occurrence of tectonic breccia and clays, with the occurrence of intense disturbances - called for the construction of the grouting curtain in the dam’s subsoil. Its depth is about 20 in the area of the riverine plain, and about 60 m in the areas of abutments. During foregoing operations of the structure, more than 30 years, local anomalies in the uplift development in the right abutment’s subsoil of the lower reservoir dam were recorded. Their abnormally high values on the downstream side of grouting curtain have become the subject of extensive discussion and a stimulus for its remediation. To ensure reliable operation of the hydraulic structure a comprehensive analysis of the impact of the long-term operation of the reservoir on the dam safety was carried out. This included an examination of the causes of anomalous development of uplifts using FEM numerical modelling. The paper presents obtained results from this analysis.
Hansley, Paula L.; Johnson, Ronald C.
1980-01-01
This report presents preliminary results of a mineralogic and diagenetic study of some low-permeability sandstones from measured surface sections and cores obtained from drill holes in the Piceance Creek Basin of northwestern Colorado. A documentation of the mineralogy and diagenetic history will aid in the exploration for natural gas and in the development of recovery technology in these low-permability sandstones. These sandstones are in the nonmarine upper part of the Mesaverde Formation (or Group) of Late Cretaceous age and are separated from overlying lower Tertiary rocks by a major regional unconformity. Attention is focused on the sandstone units of the Ohio Creek Member, which directly underlies the unconformity; however, comparisons between the mineralogy of the Ohio Creek strata and that of the underlying sandstone units are made whenever possible. The Ohio Creek is a member of the Hunter Canyon Formation (Mesaverde Group) in the southwestern part of the basin, and the Mesaverde Formation in the southern and central parts of the basin. The detrital mineralogy is fairly constant throughout all of these nonrnarine Cretaceous sandstone units; however, in the southeastern part of the basin, there is an increase in percentage of feldspar, quartzite, and igneous rock fragments in sandstones of the Ohio Creek Member directly underlying the unconformity. In the southwestern part of the basin, sandstones of the Ohio Creek Member are very weathered and are almost-entirely comprised of quartz, chert, and kaolinite. A complex diagenetic history, partly related to the overlying unconformity, appears to be responsible for transforming these sandstones into potential gas reservoirs. The general diagenetic sequence for the entire Upper Cretaceous interval studied is interpreted to be (early to late): early(?) calcite cement, chlorite, quartz overgrowths, calcite cement, secondary porosity, analcime (surface only), kaolinite and illite, and late carbonate cements. Authigenic high-iron chlorite, which occurs on grain rims and in pore throats, is primarily responsible for the low-permeability of the subsurface sandstones of the Ohio Creek Member in the center of the basin. Kaolinite is the most abundant pore-filling authigenic clay in these sandstones, from the southwestern part of the basin and is responsible for their distinctive white-weathering color in outcrop. In the sandstones below the Ohio Creek Member, however, chlorite and kaolinite occur locally, and authigenic calcite and illite are more abundant. The occurrence and distribution of secondary porosity is one of the most important aspects of the diagenetic history of these sandstones. It is present as moldic intra- and intergranular porosity, as well as microporosity among authigenic clay pariicles. Although present locally in most sandstone units, secondary porosity is particularly common in the uppermost sandstone units and is interpreted to have formed primarily asa result ofweathering during the time represented by the Cretaceous-Tertiary unconformity.
Adsorption Characteristics of Bixin on Acid- and Alkali-Treated Kaolinite in Aprotic Solvents
Rahmalia, Winda; Fabre, Jean-François; Usman, Thamrin
2018-01-01
The adsorption of bixin in aprotic solvents onto acid- and alkali-treated kaolinite was investigated. Kaolinite was treated three times, for 6 h each, with 8 M HCl or 5 M KOH. The adsorbents were characterized by XRD, FT-IR, EDS, and BET-N2. The effects of contact time and dye concentration on adsorption capacity and kinetics, electronic transition of bixin before and after adsorption, and also mechanism of bixin-kaolinite adsorption were investigated. Dye adsorption followed pseudo-second order kinetics and was faster in acetone than in dimethyl carbonate. The best adsorption results were obtained for KOH-treated kaolinite. In both of the solvents, the adsorption isotherm followed the Langmuir model and adsorption capacity was higher in dimethyl carbonate (q m = 0.43 mg/g) than in acetone (0.29 mg/g). The adsorption capacity and kinetics of KOH-treated kaolinite (q m = 0.43 mg/g, k 2 = 3.27 g/mg·min) were better than those of HCl-treated kaolinite (q m = 0.21 mg/g, k 2 = 0.25 g/mg·min) and natural kaolinite (q m = 0.18 mg/g, k 2 = 0.32 g/mg·min). There are shift in the band position of maximum intensity of bixin after adsorption on this adsorbent. Adsorption in this system seemed to be based essentially on chemisorption due to the electrostatic interaction of bixin with the strong basic and reducing sites of kaolinite. PMID:29581720
Liaki, Christina; Rogers, Christopher D F; Boardman, David I
2008-07-01
To determine the consequences of applying electrokinetics to clay soils, in terms of mechanisms acting and resulting effects on the clay, tests were conducted in which an electrical gradient was applied across controlled specimens of English China Clay (ECC) using 'inert' electrodes and a 'Reverse Osmosis' water feed to the electrodes (i.e., to mimic electrokinetic stabilisation without the stabiliser added or electrokinetic remediation without the contaminant being present). The specimens in which electromigration was induced over time periods of 3, 7, 14 and 28 days were subsequently tested for Atterberg Limits, undrained shear strength using a hand shear vane, water content, pH, conductivity and zeta potential. Water flowed through the system from anode to cathode and directly affected the undrained shear strength of the clay. Acid and alkali fronts were created around the anode and cathode, respectively, causing changes in the pH, conductivity and zeta potential of the soil. Variations in zeta potential were linked to flocculation and dispersion of the soil particles, thus raising or depressing the Liquid Limit and Plastic Limit, and influencing the undrained shear strength. Initial weakening around the anode and cathode was replaced by a regain of strength at the anode once acidic conditions had been created, while highly alkaline conditions at the cathode induced a marked improvement in strength. A novel means of indicating strength improvement by chemical means, i.e., free from water content effects, is presented to assist in interpretation of the results.
Tanks 18 And 19-F Structural Flowable Grout Fill Material Evaluation And Recommendations
DOE Office of Scientific and Technical Information (OSTI.GOV)
Langton, C. A.; Stefanko, D. B.
2013-04-23
Cementitious grout will be used to close Tanks 18-F and 19-F. The functions of the grout are to: 1) physically stabilize the final landfill by filling the empty volume in the tanks with a non-compressible material; 2) provide a barrier for inadvertent intrusion into the tank; 3) reduce contaminant mobility by a) limiting the hydraulic conductivity of the closed tank and b) reducing contact between the residual waste and infiltrating water; and 4) providing an alkaline, chemically reducing environment in the closed tank to control speciation and solubility of selected radionuclides. The objective of this work was to identify amore » single (all-in-one) grout to stabilize and isolate the residual radionuclides in the tank, provide structural stability of the closed tank and serve as an inadvertent intruder barrier. This work was requested by V. A. Chander, High Level Waste (HLW) Tank Engineering, in HLW-TTR-2011-008. The complete task scope is provided in the Task Technical and QA Plan, SRNL-RP-2011-00587 Revision 0. The specific objectives of this task were to: 1) Identify new admixtures and dosages for formulating a zero bleed flowable tank fill material selected by HLW Tank Closure Project personnel based on earlier tank fill studies performed in 2007. The chemical admixtures used for adjusting the flow properties needed to be updated because the original admixture products are no longer available. Also, the sources of cement and fly ash have changed, and Portland cements currently available contain up to 5 wt. % limestone (calcium carbonate). 2) Prepare and evaluate the placement, compressive strength, and thermal properties of the selected formulation with new admixture dosages. 3) Identify opportunities for improving the mix selected by HLW Closure Project personnel and prepare and evaluate two potentially improved zero bleed flowable fill design concepts; one based on the reactor fill grout and the other based on a shrinkage compensating flowable fill mix design. 4) Prepare samples for hydraulic property measurements for comparison to the values in the F and H- Tank Farm Performance Assessments (PAs). 5) Identify a grout mix for the Tanks 18-F and 19-F Grout Procurement Specification [Forty, 2011 a, b, c]. Results for two flowable zero bleed structural fill concepts containing 3/8 inch gravel (70070 Series and LP#8 Series) and a sand only mix (SO Series) are provided in this report. Tank Farm Engineering and SRNL Project Management selected the 70070 mix as the base case for inclusion in Revision 0 of the Tanks 18-F and 19-F grout procurement specification [Forty 2011 a] and requested admixture recommendations and property confirmation for this formulation [Forty, 2011 b]. Lower cementitious paste mixes were formulated because the 70070 mix is over designed with respect to strength and generates more heat from hydration reactions than is desirable for mass pour application. Work was also initiated on a modification of the recommended mix which included shrinkage compensation to mitigate fast pathways caused by shrinkage cracking and poor physical bonding to the tank and ancillary equipment. Testing of this option was postponed to FY12. Mix, LP#8-16 is recommended for inclusion in the specification for furnishing and delivering tank closure grout for Tanks 18-F and 19-F [Forty, 2011 c]. A shrinkage compensating variation of this mix, LP#16C, has not been fully developed and characterized at this time.« less
Investigating the Influence of Clay Mineralogy on Stream Bank Erodibility
NASA Astrophysics Data System (ADS)
Ambers, R. K.; Stine, M. B.
2005-12-01
Soil scientists concerned with erosion of agricultural fields and geotechnical engineers concerned with the mechanical behavior of soils under different conditions have both examined the role of clay mineralogy in controlling soil/sediment properties. Fluvial geomorphologists studying stream channel erosion and stability have focused more on the effects of particle-size distribution, vegetation and rooting. The clay mineralogy of bed and bank sediment has the potential to influence cohesiveness and erodibility, however. The goal of this study is to determine the influence of clay mineralogy on the erodibility of natural stream bank sediment, utilizing techniques drawn from pedology and soil mechanics. Bank samples were collected from eleven sites in small watersheds in central and western Virginia. To obtain sediment containing a range of different clay minerals, watersheds with different types of bedrock were chosen for sampling. Rock types included mafic to felsic metamorphic and igneous rocks, shale, sandstone, and limestone. Where stream bank materials were clearly stratified, different layers were sampled separately. X-ray diffraction of the clay-fraction of the sediment indicates the presence of kaolinite, illite, vermiculite, and mixed-layer clay minerals in various abundances in the different samples. Clay content is 9-46%, as determined by the hydrometer method, and textures range from silty clay and silt loam to clay loam and sandy loam. Organic mater contents range from 1-5% by the loss-on-ignition method. Bulk density of intact sediment samples averages 1.5 g/cc. Liquid limits range from 23-41 with one sample having a value of 65; plasticity indices range from 15-22. While these tests predict that the samples would show a range of mechanical behaviors, the channel morphology at the sampling sites was not strikingly different, all having steep cut banks eroded primarily by scour with no evidence of mass movement and most having a width/depth ratio around 4.5. The ASTM pinhole test for identifying dispersive clay soils is being adapted to measure erodibility of intact and remolded sediment samples in the laboratory to look for more subtle differences in behavior under erosive conditions. Factors such as the extent and method of sample compaction are being taken into account in order to standardize the method.
Mapping advanced argillic alteration at Cuprite, Nevada, using imaging spectroscopy
Swayze, Gregg A.; Clark, Roger N.; Goetz, Alexander F.H.; Livo, K. Eric; Breit, George N.; Kruse, Fred A.; Sutley, Stephen J.; Snee, Lawrence W.; Lowers, Heather A.; Post, James L.; Stoffregen, Roger E.; Ashley, Roger P.
2014-01-01
Mineral maps based on Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) data were used to study late Miocene advanced argillic alteration at Cuprite, Nevada. Distributions of Fe-bearing minerals, clays, micas, sulfates, and carbonates were mapped using the Tetracorder spectral-shape matching system. The Al content of white micas increases toward altered areas and near intrusive rocks. Alunite composition varies from pure K to intimate mixtures of Na-K endmembers with subpixel occurrences of huangite, the Ca analogue of alunite. Intimately mixed Na-K alunite marks areas of relatively lower alteration temperature, whereas co-occurring Na-alunite and dickite may delineate relict hydrothermal conduits. The presence of dickite, halloysite, and well-ordered kaolinite, but absence of disordered kaolinite, is consistent with acidic conditions during hydrothermal alteration. Partial lichen cover on opal spectrally mimics chalcedony, limiting its detection to lichen-free areas. Pods of buddingtonite are remnants of initial quartz-adularia-smectite alteration. Thus, spectral maps provide a synoptic view of the surface mineralogy, and define a previously unrecognized early steam-heated hydrothermal event.Faulting and episodes of hydrothermal alteration at Cuprite were intimately linked to upper plate movements above the Silver Peak-Lone Mountain detachment and growth, collapse, and resurgence of the nearby Stonewall Mountain volcanic complex between 8 and 5 Ma. Isotopic dating indicates that hydrothermal activity started at least by 7.61 Ma and ended by about 6.2 Ma. Spectral and stable isotope data suggest that Cuprite is a late Miocene low-sulfidation adularia-sericite type hot spring deposit overprinted by late-stage, steam-heated advanced argillic alteration formed along the margin of the Stonewall Mountain caldera.
On sorption and swelling of CO 2 in clays
Busch, A.; Bertier, P.; Gensterblum, Y.; ...
2016-03-23
One well-studied technology is the geological storage of carbon dioxide (CO 2), and a number of demonstration projects around the world have proven its feasibility and challenges. Storage conformance and seal integrity are among the most important aspects, as they determine risk of leakage as well as limits for storage capacity and injectivity. By providing evidence for safe storage is critical for improving public acceptance. Most caprocks are composed of clays as dominant mineral type which can typically be illite, kaolinite, chlorite or smectite. A number of recent studies addressed the interaction between CO 2 and these different clays andmore » it was shown that clay minerals adsorb considerable quantities of CO 2. For smectite this uptake can lead to volumetric expansion followed by the generation of swelling pressures. On the one hand CO 2 adsorption traps CO 2, on the other hand swelling pressures can potentially change local stress regimes and in unfavourable situations shear-type failure is assumed to occur. Moreover, for storage in a reservoir having high clay contents the CO 2 uptake can add to storage capacity which is widely underestimated so far. Smectite-rich seals in direct contact with a dry CO 2 plume at the interface to the reservoir might dehydrate leading to dehydration cracks. Such dehydration cracks can provide pathways for CO 2 ingress and further accelerate dewatering and penetration of the seal by supercritical CO 2. At the same time, swelling may also lead to the closure of fractures or the reduction of fracture apertures, thereby improving seal integrity. Finally, the goal of this communication is to theoretically evaluate and discuss these scenarios in greater detail in terms of phenomenological mechanisms, but also in terms of potential risks or benefits for carbon storage.« less
Rodríguez-Cruz, M S; Sánchez-Martín, M J; Andrades, M S; Sánchez-Camazano, M
2007-01-10
In this work, the efficiency of reactive clay barriers in the immobilisation of organic pesticides in a sandy soil was studied. Reactive barriers were prepared by modification of montmorillonite, kaolinite and palygorskite clay minerals, and of a clayey soil with the cationic surfactant octadecyltrimethylammonium bromide (ODTMA). Percolation curves of the pesticides linuron, atrazine and metalaxyl of different hydrophobic character, were obtained in columns packed with a natural sandy soil with these barriers intercalated under saturated flow conditions. The cumulative curves in the unmodified soil indicated a leaching of pesticides greater than 85% of the total amount of compound added. After barrier intercalation, the breakthrough curves (BTC) indicated a dramatic decrease in the amounts of linuron leached in all columns and a significant modification of the leaching kinetics of atrazine and metalaxyl. Retardation factors, R, of the pesticides in the columns were significantly correlated with the organic matter content (OM) derived from the ODTMA of the organo clay/soil barriers (r2>or=0.78). Significant correlations were also found between these R factors and the pore volume values corresponding to the maximum peaks of the BTCs (r2=0.83; p<0.01) or the total volumes leached (r2=0.44; p<0.05) for the pesticides atrazine and metalaxyl. The results obtained point to the interest in the use of reactive clay barriers for almost complete immobilisation of hydrophobic pesticides or for decreasing the leaching of moderately hydrophobic pesticides coming from point-like sources of pollution. These barriers would avoid the generation of elevated concentrations of these compounds in the soils due to their rapid washing.
NASA Astrophysics Data System (ADS)
Benetoli, Luís O. B.; de Souza, Cláudio M. D.; da Silva, Klébson L.; de Souza, Ivan G.; de Santana, Henrique; Paesano, Andrea; da Costa, Antonio C. S.; Zaia, Cássia Thaïs B. V.; Zaia, Dimas A. M.
2007-12-01
In the present paper, the adsorption of amino acids (Ala, Met, Gln, Cys, Asp, Lys, His) on clays (bentonite, kaolinite) was studied at different pH (3.00, 6.00, 8.00). The amino acids were dissolved in seawater, which contains the major elements. There were two main findings in this study. First, amino acids with a charged R group (Asp, Lys, His) and Cys were adsorbed on clays more than Ala, Met and Gln (uncharged R groups). However, 74% of the amino acids in the proteins of modern organisms have uncharged R groups. These results raise some questions about the role of minerals in providing a prebiotic concentration mechanism for amino acids. Several mechanisms are also discussed that could produce peptide with a greater proportion of amino acids with uncharged R groups. Second, Cys could play an important role in prebiotic chemistry besides participating in the structure of peptides/proteins. The FT-IR spectra showed that the adsorption of amino acids on the clays occurs through the amine group. However, the Cys/clay interaction occurs through the sulfhydryl and amine groups. X-ray diffractometry showed that pH affects the bentonite interlayer, and at pH 3.00 the expansion of Cys/bentonite was greater than that of the samples of ethylene glycol/bentonite saturated with Mg. The Mössbauer spectrum for the sample with absorbed Cys showed a large increase (˜20%) in ferrous ions. This means that Cys was able to partially reduce iron present in bentonite. This result is similar to that which occurs with aconitase where the ferric ions are reduced to Fe 2.5.
NASA Astrophysics Data System (ADS)
Ye, Chengcheng; Yang, Yibo; Fang, Xiaomin; Hong, Hanlie; Zhang, Weilin; Yang, Rongsheng; Song, Bowen; Zhang, Zhiguo
2018-03-01
Palygorskite is a widely used indicator of semiarid to arid environments in paleoclimate studies. In this study, we present detailed mineralogical and geochemical investigations exploring the genesis of palygorskite found in Eocene fluvial sediment in the northern Qaidam Basin on the northeastern Tibetan Plateau. The presence of two types of palygorskite is revealed, based on their crystallinity characteristics and distinctive rare earth element (REE) patterns in the coexisting clay fraction. Well-crystallized palygorskite samples are characterized by remarkably negative Ce anomalies and obvious middle rare earth element enrichment. Poorly crystallized palygorskite samples generally exhibit positive Ce anomalies and less pronounced middle rare earth element enrichment, which resemble those of nonpalygorskite-bearing clay samples. Given the presence of an overall oxidized fluvial sedimentary environment, we attribute the well-crystallized palygorskite (which has textures comprising long, interwoven fibers) to direct precipitation (i.e., neoformation) occurring within a reducing environment during early/postdepositional processes while the poorly crystallized palygorskite (which is characterized by short, club-shaped single crystals) originates as catchment-delivered detritus. These poorly crystallized palygorskites occur mostly in 49.5-47.0 Ma and are accompanied by decreasing kaolinite content, increasing chlorite content, and abundant xerophytic spore-pollen from the Qaidam Basin, and its neighboring Xining Basin. Collectively, these evidences suggest that a less humid climate followed after the Early Eocene Climate Optimum.
NASA Astrophysics Data System (ADS)
Truche, Laurent; Joubert, Gilles; Dargent, Maxime; Martz, Pierre; Cathelineau, Michel; Rigaudier, Thomas; Quirt, David
2018-07-01
Hydrogen (H2)-rich fluids are observed in a wide variety of geologic settings including gas seeps in serpentinized ultramafic rocks, sub-seafloor hydrothermal vents, fracture networks in crystalline rocks from continental and oceanic crust, and volcanic gases. Natural hydrogen sources can sustain deep microbial ecosystems, induce abiotic hydrocarbons synthesis and trigger the formation of prebiotic organic compounds. However, due to its extreme mobility and small size, hydrogen is not easily trapped in the crust. If not rapidly consumed by redox reactions mediated by bacteria or suitable mineral catalysts it diffuses through the rocks and migrates toward the surface. Therefore, H2 is not supposed to accumulate in the crust. We challenge this view by demonstrating that significant amount of H2 may be adsorbed by clay minerals and remain trapped beneath the surface. Here, we report for the first time H2 content in clay-rich rocks, mainly composed of illite, chlorite, and kaolinite from the Cigar Lake uranium ore deposit (northern Saskatchewan, Canada). Thermal desorption measurements reveal that H2 is enriched up to 500 ppm (i.e. 0.25 mol kg-1 of rock) in these water-saturated rocks having a very low total organic content (<0.5 wt%). Such hydrogen uptake is comparable and even exceeds adsorbed methane capacities reported elsewhere for pure clay minerals or shales. Sudoite (Al-Mg di-trioctahedral chlorite) is probably the main mineral responsible for H2 adsorption in the present case. The presence of multiple binding sites in interlinked nanopores between crystal layers of illite-chlorite particles offers the ideal conditions for hydrogen sorption. We demonstrate that 4 to 17% of H2 produced by water radiolysis over the 1.4-Ga-lifetime of the Cigar Lake uranium ore deposit has been trapped in the surrounding clay alteration haloes. As a result, sorption processes on layered silicates must not be overlooked as they may exert an important control on the fate and mobility of H2 in the crust. Furthermore, the high capacity of clay minerals to sorb molecular hydrogen may also open up new opportunities for exploration of unexpected energy resources and for H2 storage based on geo-inspired materials.
Using Frozen Barriers for Containment of Contaminants
2017-09-21
barriers are constructed of grout slurry and plastic or steel sheet pilings. Circumferential barriers can be used to completely enclose a source of...2.1.1 Slurry walls A soil-bentonite slurry trench cutoff wall (slurry wall) is excavated and backfilled with grout, cement , or soil-bentonite...installation requires a mixing area, and there is a substantial amount of excavation and the need to dispose of spoil. The advantages of cement -based
Extraction of hydrothermal alterations from ASTER SWIR data from east Zanjan, northern Iran
NASA Astrophysics Data System (ADS)
Azizi, H.; Tarverdi, M. A.; Akbarpour, A.
2010-07-01
The use of satellite images for mineral exploration has been very successful in pointing out the presence of minerals such as smectite and kaolinite which are important in the identification of hydrothermal alterations. Shortwave infrared (SWIR) bands from Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) with the wavelength of ASTER SWIR bands between 1.65 and 2.43 μm has a good potential for mapping a hydrothermal alteration minerals such as alunite, pyrophyllite, kaolinite, illite-muscovite-sericite, and carbonate. In this range, hydroxide minerals which have been produced by hydrothermal alteration exhibit good absorption compared to shorter or longer wavelengths. In this research which aims to remove atmospheric and topographic effects from ASTER SWIR data, the authors used the log-residual method (LRM) with the minimum noise fraction (MNF) transformation to create a pixel purity index (PPI) which was used to extract the most spectrally pure pixels from multispectral images. Spectral analyses of the clay mineralogy of the study area (east Zanjan, in northern Iran) were obtained by matching the unknown spectra of the purest pixels to the U.S. Geological Survey (USGS) mineral library. Three methods, spectral feature fitting (SFF), spectral angle mapping (SAM), and binary encoding (BE) were used to generate a score between 0 and 1, where a value of 1 indicates a perfect match showing the exact mineral type. In this way, it was possible to identify certain mineral classes, including chlorite, carbonate, calcite-dolomite-magnesite, kaolinite-smectite, alunite, and illite. In this research, two main propylitic and phyllic-argillic zones could be separated using their compositions of these minerals. These two alteration zones are important for porphyry copper deposits and gold mineralization in this part of Iran.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Herbst, A.K.; Rogers, A.Z.; McCray, J.A.
The Low-Activity Waste Process Technology Program at the Idaho Nuclear Technology and Engineering Center (INTEC) anticipates that large volumes of low-level/low-activity wastes will need to be grouted prior to near-surface disposal. During fiscal year 1998, three grout formulations were studied for low-activity wastes derived from INTEC liquid sodium-bearing waste. Compressive strength and leach results are presented for phosphate bonding cement, acidic grout, and alkaline grout formulations. In an additional study, grout formulations are recommended for stabilization of the INTEC underground storage tank residual heels.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Johnson, Ch.; Cange, J.; Lambert, R.
In the early to mid-1960's, liquid low-level wastes (LLLW) generated at Oak Ridge National Laboratory were disposed of in specially-constructed, gravel-filled trenches within the Melton Valley watershed at the lab. The initial selected remedy for Trenches 5 and 7 was in situ vitrification; however, an amendment to the record of decision changed the remedy to in situ grouting of the trenches. The work was accomplished by filling the void space within the crushed stone section of each trench with cementitious grout. The contaminated soil surrounding the trenches (1-m perimeter) was then grouted with acrylamide grout. At the HRE fuel wells,more » a 1-m ring of soil surrounding the fuel wells was grouted with acrylamide. The results of the hydraulic conductivity tests ranged from 4.74 x 10{sup -6} to 3.60 x 10{sup -7} cm/sec, values that were well below the 1 x 10{sup -5} cm/sec design criterion. In summary: The ISG Project was conducted to decrease hydraulic conductivity and thereby decrease water flow and contaminate migration from the area of the trenches. The initial remedy for Trenches 5 and 7 in the Melton Valley ROD was for in situ vitrification of the trench matrix. The remedy was changed to in situ grouting of the trenches and HRE fuel wells through an amendment to the ROD after moisture was found in the trenches. The grouting of the trenches was accomplished by filling the void space within the crushed stone section of each trench with cementitious grout. The contaminated soil surrounding the trenches (1-m perimeter) was then grouted with acrylamide grout to further reduce water infiltration. Soil backfill above each of the seven HRE fuel wells was removed to a depth of approximately 1 m by augering, and the soils were replaced with a cement plug to prevent water infiltration from migrating down the original borehole. Soil surrounding the fuel wells was then grouted with acrylamide to ensure water infiltration through the HRE fuel wells is prevented. A summary of the quantities used is shown. After completion of grouting, in-situ hydraulic conductivities of the grouted materials were measured to verify attainment of the design objective. The areas were then covered with multi-layer caps as part of the MV hydrologic isolation project. (authors)« less
NASA Astrophysics Data System (ADS)
Black, Sarah R.; Hynek, Brian M.
2018-06-01
Interpretation of Martian geology relies heavily on our understanding of terrestrial analog deposits and our ability to obtain comprehensive and accurate mineralogical compositions. Many previous studies of terrestrial hydrothermal deposits relied on limited datasets and/or did not use instruments analogous to those deployed on Mars. We analyzed 100 hydrothermally altered basalts from Costa Rica, Nicaragua, and Iceland with Mars analog Visible to Short Wave Infrared (VSWIR) spectroscopy, X-ray Diffraction (XRD), and Raman laser spectrometry. Alteration mineralogy consisted of amorphous and crystalline SiO2 (cristobalite, tridymite, quartz), Ca/Al/Fe/Mg-sulfates (gypsum, anhydrite, alunite, jarosite, hexahydrite, alunogen), Fe-, Ti-, and Mg-oxides/hydroxides (hematite, goethite, anatase/brookite, brucite), elemental sulfur, and phyllosilicates (montmorillonite, kaolinite). Results indicate VSWIR is best suited for identification of X-ray amorphous materials such as hydrated SiO2 and phyllosilicates, while XRD is best utilized for highly ordered crystalline materials such as sulfates, crystalline SiO2 polymorphs, elemental sulfur, and Mg-hydroxides identification. Surprisingly, XRD had the lowest identification rates for Fe-oxides/hydroxides (42% compared to 61% and 75% for VNIR and Raman, respectively), and nearly equal identification rates as VSWIR for kaolinite (76% for VSWIR, 71% for XRD). Identification of phyllosilicates in XRD, while possible, is not as effective as VSWIR without extensive sample preparation. Our observed identification rates may be attributed to the relative abundance of materials-Fe-oxides/hydroxides being present as surface coatings, the presence of large amounts of kaolinite in some samples, and an increased particle size for kaolinite relative to other clays. Elemental sulfur and Fe- and Ti-oxides/hydroxides were more readily identified with Raman. With NASA's current focus on habitability, hydrothermally altered areas-which we know to host a wide range of microbial life here on Earth-are of high interest and it is likely that future rovers will encounter similar mineral assemblages. Therefore, future rovers would benefit from using a combination of these methods and expanding the VSWIR sampling range to the full 300-2500 nm to conduct a comprehensive mineralogical investigation.
Fractionation of aquatic natural organic matter upon sorption to goethite and kaolinite
Meier, M.; Namjesnik-Dejanovic, K.; Maurice, P.A.; Chin, Y.-P.; Aiken, G.R.
1999-01-01
Natural organic matter (NOM) consists of a complex mixture of organic molecules; previous studies have suggested that preferential sorption of higher molecular weight, more hydrophobic, and more aromatic components may lead to fractionation of the NOM pool upon passage through porous media. Our work expands upon previous studies by quantifying the change in solution-phase weight average molecular weight (M(w)) upon sorption of bulk (rather than isolated) surface water NOM from the Suwannee River (SR) and the Great Dismal Swamp (GDS) to goethite and kaolinite at different sorption densities and at pH 4, 22??C. High pressure size exclusion chromatography (HPSEC) was used to quantify changes in M(w) upon sorption, and molar absorptivities at ?? = 280 nm were used to approximate changes in solution NOM aromaticity. Two SR water samples were used, with M(w) = 2320 and 2200 Da; a single GDS sample was used, with M(w) = 1890 Da. The SR NOM was slightly more hydrophobic and aromatic. These differences were reflected in greater sorption of SR NOM than GDS NOM. Both surface water NOMs showed a much greater affinity for goethite than for kaolinite. HPSEC analysis of the NOM remaining in solution after 24 h reaction time with geothite revealed that the largest changes in solution phase M(w)s (decreases by 900-1700 Da) occurred at relatively low equilibrium sorbate concentrations (approximately 5-20 mg C 1-1); the decrease in solution M(w) suggested that reactive surface sites were occupied disproportionately by large and intermediate size NOM moieties. At higher equilibrium NOM concentrations (>20 mg C 1-1), as percent adsorption decreased, M(w) in solution was similar to original samples. A smaller decrease in solution NOM M(w) (300-500 Da at 10-20 mg C 1-1 ~ 100 Da at > 20 mg) also occurred upon sorption to kaolinite. Overall, our results showed that factors (as related to NOM composition, clay mineral surface properties, and position along the sorption isotherm) which promote a higher percent sorption lead to the most pronounced decreases in solution M(w).
TANKS 18 AND 19-F STRUCTURAL FLOWABLE GROUT FILL MATERIAL EVALUATION AND RECOMMENDATIONS
DOE Office of Scientific and Technical Information (OSTI.GOV)
Stefanko, D.; Langton, C.
2011-11-01
Cementitious grout will be used to close Tanks 18-F and 19-F. The functions of the grout are to: (1) physically stabilize the final landfill by filling the empty volume in the tanks with a non compressible material; (2) provide a barrier for inadvertent intrusion into the tank; (3) reduce contaminant mobility by (a) limiting the hydraulic conductivity of the closed tank and (b) reducing contact between the residual waste and infiltrating water; and (4) providing an alkaline, chemically reducing environment in the closed tank to control speciation and solubility of selected radionuclides. The objective of this work was to identifymore » a single (all-in-one) grout to stabilize and isolate the residual radionuclides in the tank, provide structural stability of the closed tank and serve as an inadvertent intruder barrier. This work was requested by V. A. Chander, High Level Waste (HLW) Tank Engineering, in HLW-TTR-2011-008. The complete task scope is provided in the Task Technical and QA Plan, SRNL-RP-2011-00587 Revision 0. The specific objectives of this task were to: (1) Identify new admixtures and dosages for formulating a zero bleed flowable tank fill material selected by HLW Tank Closure Project personnel based on earlier tank fill studies performed in 2007. The chemical admixtures used for adjusting the flow properties needed to be updated because the original admixture products are no longer available. Also, the sources of cement and fly ash have changed, and Portland cements currently available contain up to 5 wt. % limestone (calcium carbonate). (2) Prepare and evaluate the placement, compressive strength, and thermal properties of the selected formulation with new admixture dosages. (3) Identify opportunities for improving the mix selected by HLW Closure Project personnel and prepare and evaluate two potentially improved zero bleed flowable fill design concepts; one based on the reactor fill grout and the other based on a shrinkage compensating flowable fill mix design. (4) Prepare samples for hydraulic property measurements for comparison to the values in the F and H- Tank Farm Performance Assessments (PAs). (5) Identify a grout mix for the Tanks 18-F and 19-F Grout Procurement Specification [Forty, 2011 a, b, c]. Results for two flowable zero bleed structural fill concepts containing 3/8 inch gravel (70070 Series and LP-8 Series) and a sand only mix (SO Series) are provided in this report. Tank Farm Engineering and SRNL Project Management selected the 70070 mix as the base case for inclusion in Revision 0 of the Tanks 18-F and 19-F grout procurement specification [Forty 2011 a] and requested admixture recommendations and property confirmation for this formulation [Forty, 2011 b]. Lower cementitious paste mixes were formulated because the 70070 mix is over designed with respect to strength and generates more heat from hydration reactions than is desirable for mass pour application. Work was also initiated on a modification of the recommended mix which included shrinkage compensation to mitigate fast pathways caused by shrinkage cracking and poor physical bonding to the tank and ancillary equipment. Testing of this option was postponed to FY12.« less
Karim, Mohamed Rehan; Mahmud, Hilmi; Mashaan, Nuha S.; Katman, Herdayati; Husain, Nadiah Md
2014-01-01
Semi-flexible pavement surfacing is a composite pavement that utilizes the porous pavement structure of the flexible bituminous pavement, which is subsequently grouted with appropriate cementitious materials. This study aims to investigate the compressive strength, flexural strength, and workability performance of cementitious grout. The grout mixtures are designed to achieve high strength and maintain flow properties in order to allow the cement slurries to infiltrate easily through unfilled compacted skeletons. A paired-sample t-test was carried out to find out whether water/cement ratio, SP percentages, and use of silica fume influence the cementitious grout performance. The findings showed that the replacement of 5% silica fume with an adequate amount of superplasticizer and water/cement ratio was beneficial in improving the properties of the cementitious grout. PMID:24526911
Koting, Suhana; Karim, Mohamed Rehan; Mahmud, Hilmi; Mashaan, Nuha S; Ibrahim, Mohd Rasdan; Katman, Herdayati; Husain, Nadiah Md
2014-01-01
Semi-flexible pavement surfacing is a composite pavement that utilizes the porous pavement structure of the flexible bituminous pavement, which is subsequently grouted with appropriate cementitious materials. This study aims to investigate the compressive strength, flexural strength, and workability performance of cementitious grout. The grout mixtures are designed to achieve high strength and maintain flow properties in order to allow the cement slurries to infiltrate easily through unfilled compacted skeletons. A paired-sample t-test was carried out to find out whether water/cement ratio, SP percentages, and use of silica fume influence the cementitious grout performance. The findings showed that the replacement of 5% silica fume with an adequate amount of superplasticizer and water/cement ratio was beneficial in improving the properties of the cementitious grout.
Farooq, Muhammad; Kim, Jung Ho; Song, Young Soo; Amjad Sabir, Mohammad; Umar, Muhammad; Tariq, Mohammad; Muhammad, Said
2014-01-01
The highway of Yongweol-ri, Muan-gun, south-western part of the South Korean Peninsula, is underlain by the abandoned of subsurface cavities, which were discovered in 2005. These cavities lie at shallow depths with the range of 5∼15 meters below the ground surface. Numerous subsidence events have repeatedly occurred in the past few years, damaging infrastructure and highway. As a result of continuing subsidence issues, the Korean Institute of Geosciences and Mineral Resources (KIGAM) was requested by local administration to resolve the issue. The KIGAM used geophysical methods to delineate subsurface cavities and improve more refined understanding of the cavities network in the study area. Cement based grouting has been widely employed in the construction industry to reinforce subsurface ground. In this research work, time-lapse electrical resistivity surveys were accomplished to monitor the grouting injection in the subsurface cavities beneath the highway, which have provided a quasi-real-time monitoring for modifying the subsurface cavities related to ground reinforcement, which would be difficult with direct methods. The results obtained from time-lapse electrical resistivity technique have satisfactory imaged the grouting injection experiment in the subsurface cavities beneath the highway. Furthermore, the borehole camera confirmed the presence of grouting material in the subsurface cavities, and hence this procedure increases the mechanical resistance of subsurface cavities below the highway. PMID:24578621
Farooq, Muhammad; Park, Samgyu; Kim, Jung Ho; Song, Young Soo; Amjad Sabir, Mohammad; Umar, Muhammad; Tariq, Mohammad; Muhammad, Said
2014-01-01
The highway of Yongweol-ri, Muan-gun, south-western part of the South Korean Peninsula, is underlain by the abandoned of subsurface cavities, which were discovered in 2005. These cavities lie at shallow depths with the range of 5∼15 meters below the ground surface. Numerous subsidence events have repeatedly occurred in the past few years, damaging infrastructure and highway. As a result of continuing subsidence issues, the Korean Institute of Geosciences and Mineral Resources (KIGAM) was requested by local administration to resolve the issue. The KIGAM used geophysical methods to delineate subsurface cavities and improve more refined understanding of the cavities network in the study area. Cement based grouting has been widely employed in the construction industry to reinforce subsurface ground. In this research work, time-lapse electrical resistivity surveys were accomplished to monitor the grouting injection in the subsurface cavities beneath the highway, which have provided a quasi-real-time monitoring for modifying the subsurface cavities related to ground reinforcement, which would be difficult with direct methods. The results obtained from time-lapse electrical resistivity technique have satisfactory imaged the grouting injection experiment in the subsurface cavities beneath the highway. Furthermore, the borehole camera confirmed the presence of grouting material in the subsurface cavities, and hence this procedure increases the mechanical resistance of subsurface cavities below the highway.
Effects of Coal Gangue on Cement Grouting Material Properties
NASA Astrophysics Data System (ADS)
Liu, J. Y.; Chen, H. X.
2018-05-01
The coal gangue is one of the most abundant industrial solid wastes and pollute source of air and water. The use of coal gangue in the production of cement grouting material comforms to the basic state policy of environment protection and the circular using of natural resources. Through coal gangue processing experiment, coal gangue cement grouting materials making test, properties detection of properties and theoretical analysis, the paper studied the effects of coal gangue on the properties of cement grouting materials. It is found that at the range of 600 to 700 °C, the fluidity and the compressive and flexural strengths of the cement grouting materials increase with the rising up of the calcination temperatures of coal gangue. The optimum calcination temperature is around 700 °C. The part substitution of cement by the calcined coal gangue in the cement grouting material will improve the mechanical properties of the cement grouting material, even thought it will decrease its fluidity. The best substitution amount of cement by coal gangue is about 30%. The fluidity and the long term strength of the ordinary silicate cement grouting material is obviously higher than that of the sulphoaluminate cement one as well as that of the silicate-sulphoaluminate complex cement one.
Syngouna, Vasiliki I; Chrysikopoulos, Constantinos V
2016-03-01
The cotransport of clay colloids and viruses in vertically oriented laboratory columns packed with glass beads was investigated. Bacteriophages MS2 and ΦX174 were used as model viruses, and kaolinite (ΚGa-1b) and montmorillonite (STx-1b) as model clay colloids. A steady flow rate of Q=1.5 mL/min was applied in both vertical up (VU) and vertical down (VD) flow directions. In the presence of KGa-1b, estimated mass recovery values for both viruses were higher for VD than VU flow direction, while in the presence of STx-1b the opposite was observed. However, for all cases examined, the produced mass of viruses attached onto suspended clay particles were higher for VD than VU flow direction, suggesting that the flow direction significantly influences virus attachment onto clays, as well as packed column retention of viruses attached onto suspended clays. KGa-1b hindered the transport of ΦX174 under VD flow, while STx-1b facilitated the transport of ΦX174 under both VU and VD flow directions. Moreover, KGa-1b and STx-1b facilitated the transport of MS2 in most of the cases examined except of the case where KGa-1b was present under VD flow. Also, the experimental data were used for the estimation of virus surface-coverages and virus surface concentrations generated by virus diffusion-limited attachment, as well as virus attachment due to sedimentation. Both sedimentation and diffusion limited virus attachment were higher for VD than VU flow, except the case of MS2 and STx-1b cotransport. The diffusion-limited attachment was higher for MS2 than ΦΧ174 for all cases examined. Copyright © 2015 Elsevier B.V. All rights reserved.
Chemistry of the Marlboro Clay in Virginia and Implications for the Paleocene-Eocene Thermal Maximum
NASA Astrophysics Data System (ADS)
Zimmer, M.; Cai, Y.; Corley, A.; Liang, J. A.; Powars, D.; Goldstein, S. L.; Kent, D. V.; Broecker, W. S.
2017-12-01
The Paleocene-Eocene Thermal Maximum (PETM) was a global hyperthermal ( 5ºC warming) event marked by a rapid carbon isotope excursion (CIE) of >1‰ in the marine carbonate record (e.g. Zeebe et al. Nature Geoscience 2009). Possible explanations for the CIE include intrusion of a sill complex into organic carbonate (Aarnes et al. J. Geol. Soc. 2015), dissolution of methane hydrates (Thomas et al. Geology 2002), and a comet impact event (Schaller et al. Science 2016). Here we present new data across the PETM from the VirginiaDEQ-USGS Surprise Hill (SH) core, Northumberland Co., VA. We analyzed the Marlboro Clay, a thick, kaolinite-rich clay unit that marks the initiation of the PETM in the mid-Atlantic Coastal Plain of North America, as well as units above and below it. Bulk sediment records a δ13C excursion of approximately -5‰ across the CIE, while benthic foraminifera (Cibicidoides spp.) record a synchronous excursion of approximately -4.5‰. These results are consistent with other records from the New Jersey Coastal Plain (Makarova et al. Paleoceanography 2017). The excursion coincides with an increase in magnetic susceptibility, a decrease in bulk CaCO3 content, and an 2.5‰ decrease of δ18O in both the bulk sediment and benthic foraminifera of the SH core. Pb isotope analyses of the <63 μm fraction sediments indicate a unique provenance make-up for the Marlboro Clay. The results of the study thus indicate that PETM Marlboro Clay was not generated simply by intensified weathering of the same source area as the underlying Aquia Formation and overlying Nanjemoy Formation. Any hypothesis that aims to explain the mechanism that triggered the PETM must also account for the observed distinct provenance make-up of the Marlboro Clay.
Geochemical Fate and Transport of Diphenhydramine and Cetirizine in Soil
NASA Astrophysics Data System (ADS)
Wireman, R.; Rutherford, C. J.; Vulava, V. M.; Cory, W. C.
2015-12-01
Pharmaceuticals compounds presence in natural soils and water around the world has become a growing concern. These compounds are being discharged into the environment through treated wastewater or municipal sludge applications. The main goal of this study is determine their geochemical fate in natural soils. In this study we investigated sorption and transport behavior of diphenhydramine (DPH) and cetirizine (CTZ) in natural soils. These two commonly-used antihistamines are complex aromatic hydrocarbons with polar functional groups. Two clean acidic soils (pH~4.5) were used for these studies - an A-horizon soil that had higher organic matter content (OM, 7.6%) and a B-horizon soil that had lower OM (1.6%), but higher clay content (5.1%). Sorption isotherms were measured using batch reactor experiments. Data indicated that sorption was nonlinear and that it was stronger in clay-rich soils. The pKa's of DPH and CTZ are 8.98 and 8.27 respectively, i.e., these compounds are predominantly in cationic form at soil pH. In these forms, they preferentially sorb to negatively charged mineral surfaces (e.g., clay) present in the soils. Soil clay mineral characterization indicated that kaolinite was the dominant clay mineral present along with small amount of montmorillonite. The nonlinear sorption isotherms were fitted with Freundlich model. Transport behavior of both compounds was measured using glass chromatography columns. As expected both DPH and CTZ were strongly retained in the clay-rich soil as compared with OM-rich soil. The asymmetrical shape of the breakthrough curves indicated that there were likely two separate sorption sites in the soil, each with different reaction rates with each compound. A two-region advection-dispersion transport code was used to model the transport breakthrough curves. There was no evidence of transformation or degradation of the compounds during our sorption and transport studies.
Geochemical Fate and Transport of Sildenafil and Vardenafil
NASA Astrophysics Data System (ADS)
Richter, L.; Boudinot, G.; Vulava, V. M.; Cory, W. C.
2015-12-01
The geochemical fate of pharmaceuticals and their degradation products is a developing environmental field. The geologic, chemical, and biological fate of these pollutants has become very relevant with the increase in human population and the resulting increase in pollutant concentrations in the environment. In this study, we focus on sildenafil (SDF) and vardenafil (VDF), active compounds in Viagra and Levitra, respectively, two commonly used erectile dysfunction drugs. The main objective is to determine the sorption potential and transport behavior of these two compounds in natural soils. Both SDF and VDF are complex organic molecules with multiple amine functional groups in their structures. Two types of natural acidic soils (pH≈4.5), an organic-rich soil (7.6% OM) and clay-rich soil (5.1% clay) were used in this study to determine which soil components influence sorption behavior of both compounds. Sorption isotherms measured using batch reactors were nearly linear, but sorption was stronger in soil that contained higher clay content. Both compounds have multiple pKas due to the amine functional groups, the relevant pKas of SDF are 5.97 and 7.27, and those of VDF's are 4.72 and 6.21. These values indicate that these compounds likely behave as cations in soil suspensions and hence were strongly sorbed to negatively-charged clay minerals present in both soils. The clay composition in both soils is predominantly kaolinite with smaller amount of montmorillonite, both of which have a predominantly negative surface charge. Transport experiments using glass chromatography columns indicated that both compounds were more strongly retarded in the clay-rich soils. Breakthrough curves from the transport experiments were modeled using convection-dispersion transport equations. The organic matter in the soil seemed to play a less dominant role in the geochemistry in this study, but is likely to transform both compounds into derivative compounds as seen in other studies.
NASA Astrophysics Data System (ADS)
Girard, Jean-Pierre; Freyssinet, Philippe; Chazot, Gilles
2000-02-01
An integrated study of O and H isotopes in the lateritic profile of Yaou, French Guiana, was undertaken to investigate the usefulness of stable isotopes as tracers of climatic changes in continental environments. The studied profile is composed of a 27 m thick saprolite, mostly developed in the past under wet-and-dry tropical climate in association with a duricrust, overlain by a 3 m thick yellow latosol formed more recently under present equatorial hot and humid climate. δ 18O-δD values determined for weathering goethite (pseudomorphs after pyrite) and kaolinite (microcrystalline clay groundmass) throughout the 30 m deep profile reflect formation temperatures consistent with present (25°C) and realistic past climatic temperatures (20°C-30°C), indicating that weathering minerals formed in isotopic equilibrium with their genetic environment and were not subjected to significant isotope exchange after formation. A distinct shift downward (2‰ for δ 18O, 15‰ for δD) from low to high δ 18O-δD values occurs around 20 m depth in the saprolite. It is interpreted as recording the change from the past tropical to the present equatorial climate. Goethite and kaolinite in the 5-10 m thick saprolite interval immediately above the active basement weathering front are in isotopic equilibrium with modern water and must have formed under present equatorial-humid conditions. In contrast, goethite and kaolinite found higher up in the saprolite and in the duricrust formed in the past under tropical wet and dry climate from waters distinctly depleted in 18O and D relative to modern water. The marked depletion of paleo-meteoric water at Yaou most likely reflects a more contrasted or "monsoonal" character of the ancient tropical climate. The present study shows that ancient weathering minerals in lateritic profiles preserve their δ 18O-δD values and carry a time signal. The time signal is best expressed in minerals formed rapidly at the weathering front and not subjected to post-formational remobilization, such as the goethite pseudomorphs after pyrite occurring at Yaou. Groundmass kaolinite is more susceptible to partial remobilization, through successive dissolution-precipitation reactions, which may obliterate the paleoclimatic signal. Unraveling the climatic record carried by weathering minerals in old soil systems is greatly enhanced by studying both oxygen and hydrogen isotopic compositions.
Heating-freezing effects on the orientation of kaolin clay particles
Jaradat, Karam A.; Darbari, Zubin; Elbakhshwan, Mohamed; ...
2017-09-29
The effects of temperature changes on the particle orientation of a consolidated kaolin are studied using XRD experiments. Here, two sets of equipment were utilized in this study: a benchtop equipment, and a synchrotron beamline at the National Synchrotron Light Source II (NSLS-II) at Brookhaven National Laboratory. The kaolin specimens tested in the benchtop XRD were subjected to elevated and freezing temperatures ex-situ, while those used for the NSLS-II experiment were exposed to the temperature changes in-situ. The temperatures considered in this study range from freezing (-10 °C) to elevated temperature below boiling (90 °C). The thermally-induced reorientation of claymore » mineral particles is highly dependent on the relative orientation of the clay mineral particles with respect to the applied thermal gradient. For example, kaolin samples with kaolinite particles oriented perpendicular to the thermal gradient, and to the expected thermally-induced pore water flow, experience much higher particles reorientations compared to samples with particles initially oriented parallel to the thermal gradient. Lastly, freezing kaolin preserved its microstructure as ice crystals form.« less
Heating-freezing effects on the orientation of kaolin clay particles
DOE Office of Scientific and Technical Information (OSTI.GOV)
Jaradat, Karam A.; Darbari, Zubin; Elbakhshwan, Mohamed
The effects of temperature changes on the particle orientation of a consolidated kaolin are studied using XRD experiments. Here, two sets of equipment were utilized in this study: a benchtop equipment, and a synchrotron beamline at the National Synchrotron Light Source II (NSLS-II) at Brookhaven National Laboratory. The kaolin specimens tested in the benchtop XRD were subjected to elevated and freezing temperatures ex-situ, while those used for the NSLS-II experiment were exposed to the temperature changes in-situ. The temperatures considered in this study range from freezing (-10 °C) to elevated temperature below boiling (90 °C). The thermally-induced reorientation of claymore » mineral particles is highly dependent on the relative orientation of the clay mineral particles with respect to the applied thermal gradient. For example, kaolin samples with kaolinite particles oriented perpendicular to the thermal gradient, and to the expected thermally-induced pore water flow, experience much higher particles reorientations compared to samples with particles initially oriented parallel to the thermal gradient. Lastly, freezing kaolin preserved its microstructure as ice crystals form.« less
Design and Control of Chemical Grouting : Volume 1 - Construction Control
DOT National Transportation Integrated Search
1983-04-01
This report presents the results of a laboratory and field research program investigating innovative method for design and control of chemical grouting in soils. Chemical grouting practice is reviewed and standard evaluation and measurement technique...
Raman, SEM-EDS and XRPD investigations on pre-Columbian Central America "estucado" pottery
NASA Astrophysics Data System (ADS)
Casanova Municchia, Annalaura; Micheli, Mario; Ricci, Maria Antonietta; Toledo, Michelle; Bellatreccia, Fabio; Lo Mastro, Sergio; Sodo, Armida
2016-03-01
Seventeen different colored fragments from six selected pre-Columbian estucado ceramics from El Salvador have been investigated by Raman spectroscopy, scanning electron microscope coupled to an energy dispersive spectrometer (SEM/EDS) and X-ray powder diffraction (XRPD). The peculiarity of this kind of ceramics consist of the unusual presence of a white engobe, traditionally termed stucco, between the ceramic body and the decoration elements, hence the name estucado ceramics. The aim of this work was to study the unusual manufacturing technique and to identify the chemical composition of the engobe and of the pigment palette. The results showed that the stucco layer is made of clay (kaolinite) with traces of titanium oxide (anatase). Remarkably, this is the same composition of the white pigments used for the decoration layer, thus excluding an early use of natural titanium oxide as a white pigment in the estucado productions as suggested in previous investigations. Moreover, the presence of kaolinite and anatase both in the stucco and in the decoration layer suggests a cold-working or low temperature technique. The red, yellow and green decorations were realized by the use of natural ochre, while in all the blue and gray decorations Maya blue pigment was identified. Finally, an amorphous carbon pigment of vegetal origin and manganese oxide were used to obtain black pigments.
Liquid Secondary Waste Grout Formulation and Waste Form Qualification
DOE Office of Scientific and Technical Information (OSTI.GOV)
Um, Wooyong; Williams, B. D.; Snyder, Michelle M. V.
This report describes the results from liquid secondary waste (LSW) grout formulation and waste form qualification tests performed at Pacific Northwest National Laboratory (PNNL) for Washington River Protection Solutions (WRPS) to evaluate new formulations for preparing a grout waste form with high-sulfate secondary waste simulants and the release of key constituents from these grout monoliths. Specific objectives of the LSW grout formulation and waste form qualification tests described in this report focused on five activities: 1.preparing new formulations for the LSW grout waste form with high-sulfate LSW simulants and solid characterization of the cured LSW grout waste form; 2.conducting themore » U.S. Environmental Protection Agency (EPA) Method 1313 leach test (EPA 2012) on the grout prepared with the new formulations, which solidify sulfate-rich Hanford Tank Waste Treatment and Immobilization Plant (WTP) off-gas condensate secondary waste simulant, using deionized water (DIW); 3.conducting the EPA Method 1315 leach tests (EPA 2013) on the grout monoliths made with the new dry blend formulations and three LSW simulants (242-A evaporator condensate, Environmental Restoration Disposal Facility (ERDF) leachate, and WTP off-gas condensate) using two leachants, DIW and simulated Hanford Integrated Disposal Facility (IDF) Site vadose zone pore water (VZPW); 4.estimating the 99Tc desorption K d (distribution coefficient) values for 99Tc transport in oxidizing conditions to support the IDF performance assessment (PA); 5.estimating the solubility of 99Tc(IV)-bearing solid phases for 99Tc transport in reducing conditions to support the IDF PA.« less
Dimensional Stability of Grout-Type Materials Used as Connections for Prefabricated Bridge Elements
DOT National Transportation Integrated Search
2016-05-01
The research presented in this report focuses on addressing performance concerns related to dimensional stability (primarily early age shrinkage) of 11 commercially available grout-type materials. Some of these grouts, especially those classified as ...
Corrosion performance of prestressing strands in contact with dissimilar grouts.
DOT National Transportation Integrated Search
2013-01-01
To improve the corrosion protection provided to prestressing strands, anti-bleed grouts are used to fill voids in post-tensioning : ducts that result from bleeding and shrinkage of older Portland Cement grouts. Environmental differences caused by exp...
Aluminium X-ray absorption Near Edge Structure in model compounds and Earth's surface minerals
NASA Astrophysics Data System (ADS)
Ildefonse, P.; Cabaret, D.; Sainctavit, P.; Calas, G.; Flank, A.-M.; Lagarde, P.
Aluminium K-edge X-ray absorption near edge spectra (XANES) of a suite of silicate and oxides minerals consist of electronic excitations occurring in the edge region, and multiple scattering resonances at higher energies. The main XANES feature for four-fold Al is at around 2 eV lower energy than the main XANES feature for six-fold Al. This provides a useful probe for coordination numbers in clay minerals, gels, glasses or material with unknown Al-coordination number. Six-fold aluminium yields a large variety of XANES features which can be correlated with octahedral point symmetry, number of aluminium sites and distribution of Al-O distances. These three parameters may act together, and the quantitative interpretation of XANES spectra is difficult. For a low point symmetry (1), variations are mainly related to the number of Al sites and distribution of Al-O distances: pyrophyllite, one Al site, is clearly distinguished from kaolinite and gibbsite presenting two Al sites. For a given number of Al-site (1), variations are controlled by changes in point symmetry, the number of XANES features being increased as point symmetry decreases. For a given point symmetry (1) and a given number of Al site (1), variations are related to second nearest neighbours (gibbsite versus kaolinite). The amplitude of the XANES feature at about 1566 eV is a useful probe for the assessment of AlIV/Altotal ratios in 2/1 phyllosilicates. Al-K XANES has been performed on synthetic Al-bearing goethites which cannot be studied by 27Al NMR. At low Al content, Al-K XANES is very different from that of α-AlOOH but at the highest level, XANES spectrum tends to that of diaspore. Al-K XAS is thus a promising tool for the structural study of poorly ordered materials such as clay minerals and natural alumino-silicate gels together with Al-subsituted Fe-oxyhydroxides.
NASA Astrophysics Data System (ADS)
Baghdady, Ashraf R.; Howari, Fares M.; Al-Wakeel, Mohamed I.
2016-08-01
The Florida phosphate deposits in Four Corners and Hardee County mines are composed mainly of phosphate minerals and quartz in addition to subordinate proportions of feldspars, dolomite, calcite, gypsum, kaolinite, attapulgite and montmorillonite. These phosphorites contain three structurally different types of mudclasts: massive mudclasts, mudclasts with concentric structure and mudclasts consisting of agglomerates of apatite microparticles. The latter are represented by particles resembling phosphatized fossil bacteria associated with microbial filaments, and hollow apatite particles having surfacial coatings and connected to microbial filaments. The Florida phosphate particles are reworked and vary in mineral composition, color and shape. They are composed of a mixture of well-crystalline species including carbonate fluorapatite (francolite), carbonate apatite and fluorapatite. The color variation of the phosphate particles is related to difference in mineral composition, extent of diagenetic effects and reworking. The light-colored mudclasts are characterized by the presence of carbonate apatite and aluminum hydroxide phosphate minerals, whereas the dark mudclasts are rich in iron aluminum hydroxide phosphate minerals. The Florida phosphorites are suggested to be formed partially by authigenetic precipitation, replacement of the sea floor carbonate and diatomite, and microbial processes. With respect to elemental geochemistry, the analyzed particles contain small percentages of sulfur and iron which are related to the occurrence of pyrite. Traces of silica and alumina are recorded which may be attributed to the diagenetic. Some of the tested particles are relatively rich in phosphorous, fluorine, calcium, and magnesium, while poor in silicon, potassium and sulfur. Whereas, the bioclasts (especially teeth) are relatively rich in calcium, phosphorous and fluorine while poor in silicon, aluminum, magnesium and potassium. Hence, the microchemical analyses revealed that differential diagenesis affected mudclasts more than bioclasts. There is a complete compositional gradation between clay and phosphate particles which reflects their interaction. This involved kaolinitization of the phosphate particles, phosphatization of the clay mineral particles and production of silica.
Fluorescence X-ray microscopy on hydrated tributyltin-clay mineral suspensions
NASA Astrophysics Data System (ADS)
Neuhäusler, U.; Schmidt, C.; Hoch, M.; Susini, J.
2003-03-01
Using the scanning transmission X-ray microscope at ID21 beamline of the ESRF in fluorescence mode, we mapped tin at a bulk concentration of 1000 μg(Sn)/ml within hydrated tributyltin (TBT)-clay mineral (Kaolinite) dispersion with sub-300 nm spatial resolution. Using the L absorption edges of tin at 3929, 4156 and 4465 eV fluorescence radiation was excited in tin atoms with incident photon energies of 4 and 4.5 keV. When using 4 keV radiation, only tin fluorescence is excited. For 4.5 keV X rays, both the fluorescence of tin and calcium (which is present in the solid phase) can be measured. Methodologically, we were interested in assessing and proving the possibilities and limitations of fluorescence mapping using the L absorption edges of tin, where the fluorescence yield is significantly lower compared to other elements with their K edges in the same energy range. Scientifically, organotin-clay mineral interactions are of environmental concern because this factor influences significantly the distribution of toxic TBT in the aquatic System. On one hand, the half-life of TBT deposited to the sediment phase increases, and consequently the time of its bioavailability. On the other hand, the adsorption process is reversible, which means that contaminated sediments can act as a source of pollution. The adsorption and desorption effects can be studied directly with high spatial resolution and brought into connection to the surface properties of the clay mineral under study as well as to other experimental parameters, like pH or salinity.
Design and Control of Chemical Grouting : Volume 4 - Executive Summary
DOT National Transportation Integrated Search
1983-04-01
This report focuses on the engineering practice of chemical grouting, summarizing the findings of a study to improve design and control techniques for chemical grouting in soils. Improved methods for the planning, control and evaluation of chemical g...
NASA Astrophysics Data System (ADS)
Schöllhorn, Iris; Foellmi, Karl; adatte, Thierry
2016-04-01
The Early Jurassic interval witnessed different phases of paleoenvironmental change, starting with the end-Triassic mass extinction event, c. 201.4 Ma ago, which was marked by terrestrial ecosystem turnover, up to 50% loss in marine biodiversity and large turnovers in global geochemical cycles linked to the onset of Central Atlantic Magmatic Province volcanism (Raup et Sepkosky, 1982 ; Hesselbo et al., 2002 ; Deenen et al., 2010). This time interval saw equally a phase of major climate change near the Pliensbachian-Toarcian boundary, which was followed by the Early Toarcian oceanic anoxic episode (e.g., Suan et al., 2010). Previous studies mainly focused on these major and short-lived events, while the remaining intervals of the Early Jurassic received significantly less attention. Therefore, in this study, we examine the sedimentological, geochemical and environmental changes between these events on the northern Tethyan margin (Swiss Jura). With this purpose, a wide array of geochemical analyses (carbon isotope, Rock-Eval, phosphorus content, mineralogy, trace and major element content and clay analyses) and sedimentary observations has been performed on four sections and cores (Frick, Riniken, Pfaffnau and Kreuzlingen). We observed two depositional systems: (1) the Schambelen Member (lower Hettangian) and the Frick Mb. (middle Upper Sinemurian), which are characterised by organic-rich shales intercalated by tempestites; and (2) the Beggingen Member (Upper Hettangian to Lower Sinemurian) and the Grünscholz, Breitenmatt and Rietheim Members (upper Upper Sinemurian to Pliensbachian), which are composed of carbonates marked by the presence of hiati, condensed beds, phosphate- and fossil-rich strata, and erosional features, which testify to a dynamic environment characterised by overall low sediment-accumulation rates. The clay fraction, composed mainly of kaolinite, chlorite and illite, was controlled by various parameters. The rise of kaolinite in the Late Sinemurian was probably caused by a shallowing-up also shown by a decrease in phyllosilicates and an increase in the quartz content in the whole rock. The related sea-level change is probably linked to tectonically induced regional tilting. The lowest kaolinite contents are observed in the condensed sections where important remobilisation took place. The isotope and rock-eval analyses reveal also important environmental changes: (a) Two negative carbon isotope excursions measured on organic matter (CIEorg -2‰) are observed during the Early Hettangian accompanied by a change in organic matter composition, higher productivity (high hydrogen indices), anoxia (high trace element, pyrite and organic matter contents and presence of pyrite framboids; cf. also Schwab and Spangenberg, 2006) and higher weathering rates (CIA and clay mineralogy). (b) The Early Sinemurian is characterised by a +4‰ CIEorg in this sections. Nevertheless, the globality and causes of this CIE remain to be determined. (c) The Sinemurian-Pliensbachian boundary record a negative CIEorg (-3‰), followed by a positive CIE (+2‰) during the Early-Late Pliensbachian and a negative CIEorg (-1.5‰) during the Late Pliensbachian. These CIEs are also recorded in several other localities in carbonates, belemnites, wood and organic matter, and result likely from global events. These CIEs are linked to OM preservation and/or productivity changes and/or 13C-depleted carbon input(s).
Lopes, Renato P; Dillenburg, Sergio R; Schultz, Cesar L
2016-01-01
Loess consists of silt-dominated sediments that cover ~10% of the Earth's surface. In southern South America it occurs in Argentina, Bolivia, Paraguay and Uruguay, and its presence in southern Brazil was never studied in detail. Here is proposed a new lithostratigraphic unit, Cordão Formation, consisting of loess deposits in the southern Brazilian coastal plain. It consists of fine-very fine silt with subordinate sand and clay, found mostly in lowland areas between Pleistocene coastal barriers. These sediments are pale-colored (10YR hue) and forms ~1,5-2,0 meter-thick stable vertical walls. The clay minerals include illite, smectite, interstratified illite/smectite and kaolinite, the coarser fraction is mostly quartz and plagioclase. Caliche and iron-manganese nodules are also present. The only fossils found so far are rodent teeth and a tooth of a camelid (Hemiauchenia paradoxa). Luminescence ages indicate that this loess was deposited in the latest Pleistocene, between ~30 and 10 kyrs ago, and its upper portion was modified by erosion and accumulation of clay and organic matter in the Holocene. The estimated accumulation rate was ~630 g/m2/year. The probable source of this loess is the Pampean Aeolian System of Argentina and it would have been deposited by the increased aeolian processes of the last glacial.
A note on the effect of fault gouge composition on the stability of frictional sliding
Summers, R.; Byerlee, J.
1977-01-01
The frictional properties of fault gouge have been studied at confining pressures to 6 kbars. If the gouge is composed of strong materials such as crushed granite or quartz sand, the frictional strength is high, and violent stick-slip occurs at confining pressures above approximately 1.5 kbars. If the gouge is composed of minerals such as illite, kaolinite, chlorite, or antigorite, which have weak bonding forces between the structural layers, the frictional strength is slightly lower, but violent stick-slip still occurs under high confining pressure. The expanding clays, montmorillonite and vermiculite, which have free water between their structural layers, slide stably at confining pressures as high as 6.25 kbars and exhibit low friction. A similar stable behavior with lowered strength is observed in water-saturated quartz sand when the water is confined within the fault zone during deformation. The results of this series of experiments support water being the stabilizing influence when it is either (1) trapped within or between rocks of low permeability and can provide a high pore pressure when the rocks are deformed, or (2) loosely bonded in a mineral structure, as in the hydrated clays, where it can produce a pseudo-pore pressure when the clay is compressed. In both these cases, the effective stress can be reduced and the deformation stabilized. ?? 1977.
NASA Astrophysics Data System (ADS)
Stolboushkin, A. Yu; Akst, D. V.; Fomina, O. A.; Ivanov, A. I.; Syromyasov, V. A.
2017-09-01
The analysis of waste coal from mining enterprises of Kemerovo region as raw materials for production of building ceramics is given. The results of studies of material, chemical and mineralogical compositions of waste coal from Abashevskaya processing plant (Novokuznetsk) are presented. It was established that the chemical composition of waste coal refers to aluminosilicate raw materials with a high content of alumina and coloring oxides, the residual carbon content in the wastes is 12-25 %. According to the granulometric composition the waste coal is basically a sandy-dusty fraction with a small amount of clay particles (1-3 %). Additional grinding of coal waste and the introduction of a clay additive in an amount of up to 30 % are recommended. The results of the study of the mineral composition of waste coal are presented. Clay minerals are represented in the descending order by hydromuscovite, montmorillonite and kaolinite, minerals-impurities consist of quartz, feldspar fine-dispersed carbonates. The results of the investigation of ceramic-technological properties of waste coal, which belong to the group of moderately plastic low-melting raw materials, are given. As a result of a comprehensive study it was been established that with chemical, granulometric and mineralogical compositions waste coal with the reduced residual carbon can be used in the production of ceramic bricks.
NASA Astrophysics Data System (ADS)
Liu, Jianguo; Yan, Wen; Chen, Zhong; Lu, Jun
2012-09-01
Clay minerals of surface sediment samples from nine bays/harbors along northern coast of the South China Sea (SCS) are used for sediment sources and contribution estimation in the study areas. Results reveal that sediments in the study bays/harbors seem to be a mixture of sediments from the Pearl, Hanjiang River and local islands/rivers, but their clay mineral assemblage is distinct from that of Luzon and Taiwan sediments, indicating that sediments are derived mainly from the neighboring sources through riverine input and partly from localized sediments. Due to input of local sediments in the northern SCS, sediments from both east of the Leizhou Peninsula (Area IV) and next to the Pearl River estuary (PRE, Area II) have high smectite percent. Affected by riverine input of the Pearl and Hanjiang Rivers, sediments in west of the PRE (Area III) and east of the PRE (Area I) have high illite (average 47%) and kaolinite (54%) percents, respectively. Sediment contributions of various major sources to the study areas are estimated as the following: (1) the Hanjiang River provide 95% and 84% sediments in Areas I and II, respectively, (2) the Pearl River supply 79% and 29% sediments in Areas III and IV, respectively and (3) local sediments contribute the rest and reach the maximum (˜71%) in Area IV.
Huang, Qiaoyun; Wu, Huayong; Cai, Peng; Fein, Jeremy B.; Chen, Wenli
2015-01-01
Bacterial adhesion onto mineral surfaces and subsequent biofilm formation play key roles in aggregate stability, mineral weathering, and the fate of contaminants in soils. However, the mechanisms of bacteria-mineral interactions are not fully understood. Atomic force microscopy (AFM) was used to determine the adhesion forces between bacteria and goethite in water and to gain insight into the nanoscale surface morphology of the bacteria-mineral aggregates and biofilms formed on clay-sized minerals. This study yields direct evidence of a range of different association mechanisms between bacteria and minerals. All strains studied adhered predominantly to the edge surfaces of kaolinite rather than to the basal surfaces. Bacteria rarely formed aggregates with montmorillonite, but were more tightly adsorbed onto goethite surfaces. This study reports the first measured interaction force between bacteria and a clay surface, and the approach curves exhibited jump-in events with attractive forces of 97 ± 34 pN between E. coli and goethite. Bond strengthening between them occurred within 4 s to the maximum adhesion forces and energies of −3.0 ± 0.4 nN and −330 ± 43 aJ (10−18 J), respectively. Under the conditions studied, bacteria tended to form more extensive biofilms on minerals under low rather than high nutrient conditions. PMID:26585552
Application of resistivity monitoring to evaluate cement grouting effect in earth filled dam
DOE Office of Scientific and Technical Information (OSTI.GOV)
Kim, Jin-Mo; Yoon, Wang-Jung
In this paper, we applied electrical resistivity monitoring method to evaluate the cement grouting effect. There are a lot of ways to evaluate cement grouting effect. In order to do this evaluation in a great safety, high efficiency, and lower cost, resistivity monitoring is found to be the most appropriate technique. In this paper we have selected a dam site from Korea to acquire resistivity monitoring data and compare the results of inversion to estimate the cement grouting effect.
The grout/glass performance assessment code system (GPACS) with verification and benchmarking
DOE Office of Scientific and Technical Information (OSTI.GOV)
Piepho, M.G.; Sutherland, W.H.; Rittmann, P.D.
1994-12-01
GPACS is a computer code system for calculating water flow (unsaturated or saturated), solute transport, and human doses due to the slow release of contaminants from a waste form (in particular grout or glass) through an engineered system and through a vadose zone to an aquifer, well and river. This dual-purpose document is intended to serve as a user`s guide and verification/benchmark document for the Grout/Glass Performance Assessment Code system (GPACS). GPACS can be used for low-level-waste (LLW) Glass Performance Assessment and many other applications including other low-level-waste performance assessments and risk assessments. Based on all the cses presented, GPACSmore » is adequate (verified) for calculating water flow and contaminant transport in unsaturated-zone sediments and for calculating human doses via the groundwater pathway.« less
NASA Astrophysics Data System (ADS)
Zhao, Yifei; Zou, Xinqing; Gao, Jianhua; Wang, Chenglong; Li, Yali; Yao, Yulong; Zhao, Wancang; Xu, Min
2018-02-01
We examined the source-to-sink sediment transport processes from the Changjiang River to the estuarine coastal shelf area by analyzing the clay mineral assemblages in suspended sediment samples from the Changjiang River catchment and surface samples from the estuarine coastal shelf area following the impoundment of the Three Gorges Dam (TGD) in 2003. The results indicate that the clay mineral compositions throughout the study area are dominated by illite, with less abundant kaolinite and chlorite and scarce smectite. The clay minerals display distinct differences in the tributaries and exhibit obvious changes in the trunk stream compared with the periods before 2003, and the source of sediment has largely shifted to the mid- to lower reaches of the river after 2003. Spatially, the clay mineral assemblages in the estuarine area define two compositionally distinct provinces. Province I covers the mud area of the Changjiang River estuary and the Zhe-Min coastal region, where sediment is primarily supplied by the Changjiang River. Province II includes part of the Changjiang River estuary and the southeastern portion of the study area, where the sediment is composed of terrestrial material from the Changjiang River and re-suspended material from the Huanghe River carried by the Jiangsu coastal current. Moreover, the other smaller rivers in China (including the Oujiang and Minjiang rivers of mainland China and the rivers of West Taiwan) also contribut sediments to the estuarine and inner shelf areas. In general, the clay mineral assemblages in the Changjiang River estuarine area are have mainly been controlled by sediment supplied from upstream of the Changjiang River tributaries. However, since the completion of the TGD in 2003, the mid- to downstream tributaries have become the main source of sediments from the Changjiang catchment into the East China Sea. These analyses further demonstrate that the coastal currents and the decrease in the sediment load of the river have the greatest impacts on the distribution and transport of clay minerals assemblages in the sediments.
TANKS 18 AND 19-F EQUIPMENT GROUT FILL MATERIAL EVALUATION AND RECOMMENDATIONS
DOE Office of Scientific and Technical Information (OSTI.GOV)
Stefanko, D.; Langton, C.
The United States Department of Energy (US DOE) intends to remove Tanks 18-F and 19-F at the Savannah River Site (SRS) from service. The high-level waste (HLW) tanks have been isolated from the F-area Tank Farm (FTF) facilities and will be filled with cementitious grout for the purpose of: (1) physically stabilizing the empty volumes in the tanks, (2) limiting/eliminating vertical pathways from the surface to residual waste on the bottom of the tanks, (3) providing an intruder barrier, and (4) providing an alkaline, chemical reducing environment within the closure boundary to limit solubility of residual radionuclides. Bulk waste andmore » heel waste removal equipment will remain in Tanks 18-F and 19-F when the tanks are closed. This equipment includes: mixer pumps, transfer pumps, transfer jets, equipment support masts, sampling masts and dip tube assemblies. The current Tank 18-F and 19-F closure strategy is to grout the internal void spaces in this equipment to eliminate fast vertical pathways and slow water infiltration to the residual material on the tank floor. This report documents the results of laboratory testing performed to identify a grout formulation for filling the abandoned equipment in Tanks 18-F and 19-F. The objective of this work was to formulate a flowable grout for filling internal voids of equipment that will remain in Tanks 18-F and 19-F during the final closures. This work was requested by V. A. Chander, Tank Farm Closure Engineering, in HLW-TTR-2011-008. The scope for this task is provided in the Task Technical and Quality Assurance Plan (TTQAP), SRNL-RP-2011-00587. The specific objectives of this task were to: (1) Prepare and evaluate the SRR cooling coil grout identified in WSRC-STI-2008-00298 per the TTR for this work. The cooling coil grout is a mixture of BASF MasterFlow{reg_sign} 816 cable grout (67.67 wt. %), Grade 100 ground granulated blast furnace slag (7.52 wt. %) and water (24.81 wt. %); (2) Identify equipment grout placement and performance properties; (3) Design up to 2 additional grout systems for filling the Tank 18-F and Tank 19-F equipment; (4) Prepare samples of candidate grouts and measure fresh properties, thermal properties and cured properties; (5) Recommend a grout for the Tier 1A equipment fill mock up - ADMP 4 foot high mock up, 1 inch and 2 inch pipes; (6) Support procurement of materials for the Tier 1A equipment fill mock up test; (7) Prepare samples of the recommended grout for hydraulic property measurements which can be used for comparison to values used in the F- Tank Farm Performance Assessment (PA); and (8) Document equipment fill grout data and recommendations in a report.« less
DOE Office of Scientific and Technical Information (OSTI.GOV)
Phillips, S.J.; Phillips, M.; Etheridge, D.
2012-07-01
Per regulatory agreement and facility closure design, U.S. Department of Energy Hanford Site nuclear fuel cycle structures and materials require in situ isolation in perpetuity and/or interim physicochemical stabilization as a part of final disposal or interim waste removal, respectively. To this end, grout materials are being used to encase facilities structures or are being incorporated within structures containing hazardous and radioactive contaminants. Facilities where grout materials have been recently used for isolation and stabilization include: (1) spent fuel separations, (2) uranium trioxide calcining, (3) reactor fuel storage basin, (4) reactor fuel cooling basin transport rail tanker cars and casks,more » (5) cold vacuum drying and reactor fuel load-out, and (6) plutonium fuel metal finishing. Grout components primarily include: (1) portland cement, (2) fly ash, (3) aggregate, and (4) chemical admixtures. Mix designs for these typically include aggregate and non aggregate slurries and bulk powders. Placement equipment includes: (1) concrete piston line pump or boom pump truck for grout slurry, (2) progressive cavity and shearing vortex pump systems, and (3) extendable boom fork lift for bulk powder dry grout mix. Grout slurries placed within the interior of facilities were typically conveyed utilizing large diameter slick line and the equivalent diameter flexible high pressure concrete conveyance hose. Other facilities requirements dictated use of much smaller diameter flexible grout conveyance hose. Placement required direct operator location within facilities structures in most cases, whereas due to radiological dose concerns, placement has also been completed remotely with significant standoff distances. Grout performance during placement and subsequent to placement often required unique design. For example, grout placed in fuel basin structures to serve as interim stabilization materials required sufficient bearing i.e., unconfined compressive strength, to sustain heavy equipment yet, low breakout force to permit efficient removal by track hoe bucket or equivalent construction equipment. Further, flow of slurries through small orifice geometries of moderate head pressures was another typical design requirement. Phase separation of less than 1 percent was a typical design requirement for slurries. On the order of 30,000 cubic meters of cementitious grout have recently been placed in the above noted U.S. Department of Energy Hanford Site facilities or structures. Each has presented a unique challenge in mix design, equipment, grout injection or placement, and ultimate facility or structure performance. Unconfined compressive and shear strength, flow, density, mass attenuation coefficient, phase separation, air content, wash-out, parameters and others, unique to each facility or structure, dictate the grout mix design for each. Each mix design was tested under laboratory and scaled field conditions as a precursor to field deployment. Further, after injection or placement of each grout formulation, the material was field inspected either by standard laboratory testing protocols, direct physical evaluation, or both. (authors)« less
Dispersion of kaolinite by dissolved organic matter from Douglas-fir roots
Philip B. Durgin; Jesse G. Chaney
1984-01-01
The organic constituents of water extracts from Douglas-fir (Pseudotsuga menziesii [Mirb.] Franco var. menziesii) roots that cause kaolinite dispersion were investigated. The dissolved organic matter was fractionated according to molecular size and chemical characteristics into acids, neutrals, and bases of the hydrophilic and hydrophobic groups.
NASA Astrophysics Data System (ADS)
Londono, S. C.; Williams, L. B.
2013-12-01
The emergence of antibiotic resistant bacteria and increasing accumulations of antibiotics in reclaimed water, drive the quest for new natural antimicrobials. We are studying the antibacterial mechanism(s) of clays that have shown an ability to destroy bacteria or significantly inhibit their growth. One possible mode of action is from soluble transition metal species, particularly reduced Fe, capable of generating deleterious oxygen radical species. Yet another possibility is related to membrane damage as a consequence of physical or electrostatic interaction between clay and bacteria. Both mechanisms could combine to produce cell death. This study addresses a natural antibacterial clay from the NW Amazon basin, South America (AMZ clay). Clay mineralogy is composed of disordered kaolinite (28.9%), halloysite (17.8%) illite (12%) and smectite (16.7%). Mean particle size is 1.6μm and total and specific surface area 278.82 and 51.23 m2/g respectively. The pH of a suspension (200mg/ml) is 4.1 and its Eh is 361mV after 24h of equilibration. The ionic strength of the water in equilibrium with the clay after 24 h. is 6 x10-4M. These conditions, affect the element solubility, speciation, and interactions between clay and bacteria. Standard microbiological methods were used to assess the viability of two model bacteria (Escherichia coli and Bacillus subtilis) after incubation with clay at 37 degC for 24 hrs. A threefold reduction in bacterial viability was observed upon treatment with AMZ clay. We separated the cells from the clay using Nycodenz gradient media and observed the mounts under the TEM and SEM. Results showed several membrane anomalies and structural changes that were not observed in the control cells. Additionally, clay minerals appeared in some places attached to cell walls. Experiments showed that exchanging AMZ clay with KCl caused loss of antibacterial property. Among the exchangeable -and potentially toxic- ions we measured Al+3, Cu+2, Zn+2, Ba+2 and Co+2. Besides being toxic at high concentrations, these species affect the electrophoretic interactions between clay and bacteria surfaces. Additionally, the cation exchange neutralizes the clay surface charge thus modifying further the behavior of particles in suspension. Therefore, we evaluated the clay and bacteria zeta potential (ζ) as an index for possible electrostatic forces and modeled the total interactions using DLVO theory. We suspended the particles in water equilibrated with clay (leachate). Results show that at pH 4, the ζ of clays is -14 mV while it is -3mV for bacteria. The divalent ions and trivalent Aluminum, present in the AMZ leachate, compress the thickness of the double layer (hydration shell) thus decreasing electrostatic repulsion and allowing particles to come closer. The proximity of particles increases the probability of attractive forces to bind clays and cells. In summary, results indicate that a process other than simple chemical transfer from clay to bacteria is operating. The electrostatic attraction and physical proximity may enhance the toxic action of metals and interfere with the membrane properties or processes.
DOT National Transportation Integrated Search
2016-10-16
n Accelerated Bridge Construction (ABC) methods, one way to connect prefabricated columns is by using grouted steel bar couplers. As of October 2016, in the U.S., only Utah DOT allows the use of grouted couplers in plastic hinge locations in seismic ...
Municipalities are discovering rapid degradation of infrastructures in wastewater collection and treatment facilities due to infiltration of leaking water from the surrounding environments. Rehabilitation of these facilities by in situ methods, including the use of grouting, is u...
Municipalities are discovering rapid degradation of infrastructures in wastewater collection and treatment facilities due to infiltration of leaking water from the surrounding environments. Rehabilitation of these facilities by in situ methods, including the use of grouting, is u...
Preparation of poly(vinyl alcohol)/kaolinite nanocomposites via in situ polymerization
DOE Office of Scientific and Technical Information (OSTI.GOV)
Jia Xin; Department of Chemistry, Hexi University, Zhangye 734000; Li Yanfeng
2008-03-04
Poly(vinyl alcohol)/kaolinite intercalated nanocomposites (Kao-PVA) were prepared via in situ intercalation radical polymerization. Vinyl acetate (VAc) was intercalated into kaolinite by a displacement method using dimethyl sulfoxide/kaolinite (Kao-DMSO) as the intermediate. Then, PVAc/kaolinite (Kao-PVAc) was obtained via radical polymerization with benzoyl peroxide (BPO) as initiator. Last, PVAc/kaolinite was saponified via direct-hydrolysis with NaOH solution in order to obtain PVA/kaolinite nanocomposites, which was characterized by Fourier-Transformation spectroscopy (FTIR), wide X-ray diffraction (WXRD) and transmission electron microscopy (TEM). Their differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) results of the obtained PVA/kaolinite suggested that the thermal properties had an obvious improvement.
DOT National Transportation Integrated Search
2014-06-01
This report contains a summary of the research performed to develop a replacement for the high-temperature grout : fluidity (HTGF) test. The HTGF test was employed in the past by FDOT to qualify post-tensioning (PT) grouts for use in : post-tensioned...
Research in Foundation Grouting with Cement
1960-03-01
grout is mixed. 2. For cracks of the order of 0.05 in., a grout in which the ratio[ of water to cement is 0.75 by volune gives the r’ost desirable 4... thickness of the order of t5 in. 4. 3hear tests on grout films fog-cured at 70 F for 28 days denon- stratel that increasing the pressure within the...alkaline water dripre.I through cracks in the concrete lidng of some of the penstock tunnels Jai daaged the paint an- metal -work. The uplift pressure
1994-05-01
utilizes drill bits and tubing to cut through the soil. Unlike the auger method, a slurry mixture is used to keep the drill bit clean and assist in...is applied. In the sleeve pipe method, or also called tube -a-manchette, the sleeve pipe is installed in the grout hole, and sealed in place with a...acts as a one-way valve. allowing grout out of the pipe, but not back into the sleeve. A grouting tube with double packer is used to inject the grout
Frictional Properties of Opalinus Clay: Implications for Nuclear Waste Storage
NASA Astrophysics Data System (ADS)
Orellana, L. F.; Scuderi, M. M.; Collettini, C.; Violay, M.
2018-01-01
The kaolinite-bearing Opalinus Clay (OPA) is the host rock proposed in Switzerland for disposal of radioactive waste. However, the presence of tectonic faults intersecting the OPA formation put the long-term safety performance of the underground repository into question due to the possibility of earthquakes triggered by fault instability. In this paper, we study the frictional properties of the OPA shale. To do that, we have carried out biaxial direct shear experiments under conditions typical of nuclear waste storage. We have performed velocity steps (1-300 μm/s) and slide-hold-slide tests (1-3,000 s) on simulated fault gouge at different normal stresses (4-30 MPa). To establish the deformation mechanisms, we have analyzed the microstructures of the sheared samples through scanning electron microscopy. Our results show that peak (μpeak) and steady state friction (μss) range from 0.21 to 0.52 and 0.14 to 0.39, respectively, thus suggesting that OPA fault gouges are weak. The velocity dependence of friction indicates a velocity strengthening regime, with the friction rate parameter (a - b) that decreases with normal stress. Finally, the zero healing values imply a lack of restrengthening during interseismic periods. Taken together, if OPA fault reactivates, our experimental evidence favors an aseismic slip behavior, making the nucleation of earthquakes difficult, and long-term weakness, resulting in stable fault creeping over geological times. Based on the results, our study confirms the seismic safety of the OPA formation for a nuclear waste repository.
NASA Astrophysics Data System (ADS)
Akai, Junji; Nomura, Nao; Matsushita, Shin; Kudo, Hisaaki; Fukuhara, Haruo; Matsuoka, Shiro; Matsumoto, Jinko
Soil contamination by radioactive Cs from Fukushima Daiichi Nuclear Power Plant accident was investigated. Absorption and desorption experiments of Cs were conducted for several phyllosillicates (kaolinite, sericite, montmorillonite, vermiculite, chrysotile and biotite), zeolite and solid organic matter (dead and green leaves). The results confirmed the characteristic sorption and desorption of Cs by these materials. The 2:1 type phyllosilicate, especially, vermiculite and montmorillonite absorbed Cs well. Heated vermiculite for agricultural use and weathered montmorillonite also adsorbed Cs. Leaves also absorbed Cs considerably but easily desorbed it. In summary, the relative capacity and strength of different materials for sorption of Cs followed the order: zeolite (clinoptilolite) > 2:1 type clay mineral > 1:1 type clay mineral > dead and green leaves. Culture experiments using bacteria of both naturally living on dead leaves in Iitate village, Fukushima Pref. and bacterial strains of Bacillus subtillis, Rhodococus erythropolis, Streptomyces aomiensis and Actinomycetospora chlora were carried out. Non-radioactive 1% Cs solution (CsCl) was added to the culture media. Two types of strong or considerable bacterial uptakes of Cs were found in bacterial cells. One is that Cs was contained mainly as globules inside bacteria and the other is that Cs was absorbed in the whole bacterial cells. The globules consisted mainly of Cs and P. Based on all these results, future diffusion and re-circulation behavior of Cs in the surface environment was discussed.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Elliott, W. Crawford; Kahn, Bernd; Rosson, Robert
2011-11-14
In this exploratory project, we are testing two interrelated hypotheses about the sorption of Cs within weathered micaceous materials in subsurface regolith materials from the Savannah River Site (SRS) located on the Atlantic Coastal Plain: 1) that stable cesium has become significantly enriched relative to potassium in subsurface micaceous particles as a result of chemical weathering processes; and 2) that the Cs so present is sufficient to be a major factor determining the ability of the subsurface materials to take up and hold 137Cs. To test these hypotheses, we collected by hand augur soil samples corresponding to soils representative atmore » the SRS: upland regolith (Fuquay series); soils formed on Tobacco Road Sandstone; and, soils formed on Quaternary Alluvium. From our data, the quantification of the amounts of stable cesium concentrated in various sites within 2:1 phyllosilicates by natural processes is highly relevant toward understanding the future sorption of 137Cs by the mica, illite, vermiculite, and hydroxyl interstratified vermiculite (HIV) phases present in the subsurface at and in proximity to SRS. Studying sorption and fixation of Cs in these micaceous phases interlayers potentially leads to increased knowledge to the extent that stable Cs resists exchange with ion exchange cations (Mg, NH4, or even alkyl ammonium compounds) and to the extent that Cs can become fixed over the long term. Such knowledge will help in the development of 137Cs remediation strategies for the long-term, which is a critical aspect of the SBR goals. We characterized the mineralogy, K-Ar ages of the soil and soil clay fractions (before and after acid treatment), and alkali element chemistry (K, Rb, Cs) of the clay fractions of soils collected from these three different types of soils. The clay fractions of the Fuquay soils are composed of kaolinite, and hydroxy interstratified vermiculite (HIV). Kaolinite, HIV, quartz, gibbsite and illite are found in the quaternary soils. Leach experiments using 10% nitric acid and 50% nitric acid were performed on 62 mesh fractions to show the amounts of Cs and Rb relative to K (Cs/K, Rb/K) that are exchangeable in these soils compared to Coastal Plain micas and upper continental crust. The Cs/K and Rb/K of the leachates are considerably higher relative to both upper continental crust and relative to weathered micas found in Georgia Coast Plain sediments. The K-Ar ages of the clay fractions of five different SRS soil series were ca. 320 Ma. After leaching with nitric acid, the ages of the soil clay fractions were approximately the same as the unleached soil clays. Based on the similarity of these ages to the ages of Coastal Plain micas, the K and Ar remaining after treatment is believed to be enclosed in a relect mica in the HIV phases in the soils. The HIV is likely a mica-HIV intergrade. Based on these data, stable cesium has become significantly enriched relative to potassium in subsurface micaceous particles as a result of chemical weathering processes in the SRS Fuquay soils studied thus far. Our data permit the interpretation describing the sorption of Cs and Rb in an apex site or in a hard to reach hard-to-exchange sorption site during pedogenesis. In terms of testing the second hypothesis, our work is ongoing and we report some preliminary data on Cs-137 and Rb-85 exchange experiments on select SRS Fuquay soils (-2 mm). Our isotopic equilibration experiments using Cs and Rb isotopes in separate exchange experiments show only small amounts of Cs and Rb in the original sample is exchangeable isotopically for a period of a few weeks in acidified conditions. The isotope exchange experiments provide support for our interpretation that pedogenically accumulated Cs (and Rb) occupy sites that are unavailable to exchange or exchange slowly in acid conditions corresponding to present conditions in SRS soils. In more basic solutions, greater exchange isotopic exchange is noted and suggests an expansion of interlayer sites thereby permitting more isotopic exchange of Cs and Rb.« less
NASA Astrophysics Data System (ADS)
Chen, Jun; Min, Fan-fei; Liu, Lingyun; Liu, Chunfu; Lu, Fangqin
2017-10-01
The adsorption of four different amine/ammonium salts of DDA (Dodecyl amine), MDA (N-methyldodecyl amine), DMDA (N,N-dimethyldodecyl amine) and DTAC (Dodecyl trimethyl ammonium chloride) on kaolinite particles was investigated in the study through the measurement of contact angles, zeta potentials, aggregation observation, adsorption and sedimentation. The results show that different amine/ammonium salts can adsorb on the kaolinite surface to enhance the hydrophobicity and reduce the electronegativity of kaolinite particle surface, and thus induce a strong hydrophobic aggregation of kaolinite particles which promotes the settlement of kaolinite. To explore the adsorption mechanism of these four amine/ammonium salts on kaolinite surfaces, the adsorptions of DDA+, MDA+, DMDA+ and DTAC+ on kaolinite (001) surface and (00 1 bar) surface are calculated with DFT (Density functional theory). The DFT calculation results indicate that different amine/ammonium cations can strongly adsorbed on kaolinite (001) surface and (00 1 bar) surface by forming Nsbnd H⋯O strong hydrogen bonds or Csbnd H⋯O weak hydrogen bonds, and there are strongly electrostatic attractions between different amine/ammonium cations and kaolinite surfaces. The main adsorption mechanism of amine/ammonium cations on kaolinite is hydrogen-bond interaction and electrostatic attraction.
NASA Technical Reports Server (NTRS)
Janice, Bishop; Banin, A.; Mancinelli, R. L.; Klovstad, M. R.; DeVincenzi, Donald L. (Technical Monitor)
2001-01-01
Nitrogen is an essential element for life. It is the only element among the six major biogenic elements, C, O, S, O, P, H, whose presence in the Martian soil has not been positively and directly established. We describe here a study assessing the ability to detect NH4 in soils by two methods: differential thermal analysis (DTA) and infrared (IR) reflectance spectroscopy. Four standard clay minerals (kaolinite, montmorillonite, illite and attapulgite) and an altered tephra sample from Mauna Kea were treated with NH4 in this study. Samples of the NH4-treated and leached clays were analyzed by DTA and infrared (IR) reflectance spectroscopy to quantify the delectability of soluble and sorbed/fixed NH4. An exotherm at 270-280 C was clearly detected in the DTA curves of NH4-treated (non-leached) samples. This feature is assigned to the thermal decomposition reaction of NH4. Spectral bands observed at 1.56, 2.05, 2.12, 3.06, 3.3, 3.5, 5.7 and 7.0 microns in the reflectance spectra of NH4-treated and leached samples are assigned to the sorbed/fixed ammonium in the clays. The montmorillonite has shown the most intense absorbance due to fixed ammonium among the leached samples in this study, as a result of its high cation sorption capacity. It is concluded that the presence of sorbed or fixed NH4 in clays may be detected by infrared (IR) reflectance or emission spectroscopy. Distinction between soluble and sorbed NH4 may be achieved through the presence or absence of several spectral features assigned to the sorbed NH4 moietyi and, specifically, by use of the 4.2 micrometer feature assigned to solution NH4. Thermal analyses furnish supporting evidence of ammonia in our study through detection of N released at temperatures of 270-330 C. Based on these results it is estimated that IR spectra measured from a rover should be able to detect ammonia if present above 20 mg NH4/g sample in the surface layers. Orbital IR spectra and thermal analyses measured on a rover may be able to detect ammonia in soils as well but at higher abundances. The spectral features at 3.06 and 7.0 microns due to bound NH4 in clays and altered Hawaiian tephra appear to be the most promising for detection by orbital spectrometers. If N species are present on Mars the sedimentary deposits may be the best regions to look for them.
Zhang, Tongwei; Ellis, Geoffrey S.; Ruppel, Stephen C.; Milliken, Kitty; Lewan, Mike; Sun, Xun; Baez, Luis; Beeney, Ken; Sonnenberg, Steve
2013-01-01
A series of CH4 adsorption experiments on natural organic-rich shales, isolated kerogen, clay-rich rocks, and artificially matured Woodford Shale samples were conducted under dry conditions. Our results indicate that physisorption is a dominant process for CH4 sorption, both on organic-rich shales and clay minerals. The Brunauer–Emmett–Teller (BET) surface area of the investigated samples is linearly correlated with the CH4 sorption capacity in both organic-rich shales and clay-rich rocks. The presence of organic matter is a primary control on gas adsorption in shale-gas systems, and the gas-sorption capacity is determined by total organic carbon (TOC) content, organic-matter type, and thermal maturity. A large number of nanopores, in the 2–50 nm size range, were created during organic-matter thermal decomposition, and they significantly contributed to the surface area. Consequently, methane-sorption capacity increases with increasing thermal maturity due to the presence of nanopores produced during organic-matter decomposition. Furthermore, CH4 sorption on clay minerals is mainly controlled by the type of clay mineral present. In terms of relative CH4 sorption capacity: montmorillonite ≫ illite – smectite mixed layer > kaolinite > chlorite > illite. The effect of rock properties (organic matter content, type, maturity, and clay minerals) on CH4 adsorption can be quantified with the heat of adsorption and the standard entropy, which are determined from adsorption isotherms at different temperatures. For clay-mineral rich rocks, the heat of adsorption (q) ranges from 9.4 to 16.6 kJ/mol. These values are considerably smaller than those for CH4 adsorption on kerogen (21.9–28 kJ/mol) and organic-rich shales (15.1–18.4 kJ/mol). The standard entropy (Δs°) ranges from -64.8 to -79.5 J/mol/K for clay minerals, -68.1 to -111.3 J/mol/K for kerogen, and -76.0 to -84.6 J/mol/K for organic-rich shales. The affinity of CH4 molecules for sorption on organic matter is stronger than for most common clay minerals. Thus, it is expected that CH4 molecules may preferentially occupy surface sites on organic matter. However, active sites on clay mineral surfaces are easily blocked by water. As a consequence, organic-rich shales possess a larger CH4-sorption capacity than clay-rich rocks lacking organic matter. The thermodynamic parameters obtained in this study can be incorporated into model predictions of the maximum Langmuir pressure and CH4- sorption capacity of shales under reservoir temperature and pressure conditions.
NASA Astrophysics Data System (ADS)
Zhao, Yifei; Zou, Xinqing; Liu, Qing; Wang, Chenglong; Ge, Chendong; Xu, Min
2018-02-01
The estuarine-inner shelf mud regions of the East China Sea (ECS) are valuable for studying the source-to-sink processes of fluvial sediments deposited since the Holocene. In this study, we present evidence of the provenance and environmental evolution of two cores (S5-2 and JC07) from the estuarine-inner shelf regions of the ECS over the past 100 years based on 210Pb dating, high-resolution grain size measurements and clay mineral analyses. The results indicate that the clay mineral assemblages of cores S5-2 and JC07 are dominated by illite, followed by kaolinite and chlorite, and present scarce amounts of smectite. A comparison of these clay mineral assemblages with several major sources reveals that the fine sediments on the estuarine-inner shelf of the ECS represent a mixture of provenances associated with the Yangtze and Yellow Rivers, as well as smaller rivers. However, the contribution of each provenance has varied greatly over the past hundred years, as indicated by the down-core variability due to strong sediment reworking and transport on the inner shelf and the reduction of the sediment load from the Yangtze River basin. In the mud region of the Yangtze River estuary, the sediment from 1930 to 1956 was primarily derived from the Yangtze River, although the Yellow River was also an important influence. From 1956 to 2013, the Yellow River contribution decreased, whereas the Yangtze River contribution correspondingly increased. In the Zhe-Min mud region, the Yangtze River contributed more sediment than did other rivers from 1910 to 1950; however, the Yangtze River contribution gradually decreased from 1950 to 2013. Moreover, the other small rivers accounted for minor contributions, and the East Asian winter monsoon (EAWM) played an important role in the sediment transport process in the ECS. Our results indicate that the weakening/strengthening of the EAWM and a decrease in the sediment load of the Yangtze River influenced the transport and fate of sediment on the estuarine-inner shelf of the ECS.
Thermal Response Testing Takes a Step Forward
Clemenzi, Rick; Ewbank, Garen; Siglin, Judy; ...
2017-09-01
Oak Ridge National Labs has independently confirmed the accuracy of a new breakthrough Advanced Thermal Response Test (TRT) method that it claims “uses less than half of the test time, allows for a fluctuating or interruptible heat flux, performs quality validation of a GHEX installation, and yields new insights into ground thermal conductivity that warrant further research.” The new Advanced TRT approach will reduce costs and, for the first time, also determine the actual thermal conductivity of grout as it is installed. As everyone in the ground source heat pump (GSHP) industry knows, assuring the quality of the grout jobmore » of a ground heat exchanger (GHEX) is an especially vexing problem. Unless one is standing at the borehole head the entire time grouting is underway, they basically have no idea how good or bad the grouting job is or even if the loop pipe itself is installed correctly. This problem has been further brought to light with formal third party grout reports confirming that grout had been poured from the surface and that many loops were shorter than the specified depth in several projects« less
Thermal Response Testing Takes a Step Forward
DOE Office of Scientific and Technical Information (OSTI.GOV)
Clemenzi, Rick; Ewbank, Garen; Siglin, Judy
Oak Ridge National Labs has independently confirmed the accuracy of a new breakthrough Advanced Thermal Response Test (TRT) method that it claims “uses less than half of the test time, allows for a fluctuating or interruptible heat flux, performs quality validation of a GHEX installation, and yields new insights into ground thermal conductivity that warrant further research.” The new Advanced TRT approach will reduce costs and, for the first time, also determine the actual thermal conductivity of grout as it is installed. As everyone in the ground source heat pump (GSHP) industry knows, assuring the quality of the grout jobmore » of a ground heat exchanger (GHEX) is an especially vexing problem. Unless one is standing at the borehole head the entire time grouting is underway, they basically have no idea how good or bad the grouting job is or even if the loop pipe itself is installed correctly. This problem has been further brought to light with formal third party grout reports confirming that grout had been poured from the surface and that many loops were shorter than the specified depth in several projects« less
NASA Astrophysics Data System (ADS)
Lawrence, J.; Li, L.; Spencer, J. T.
1998-04-01
Work has been conducted using a 60 Wcw high power diode laser (HPDL) in order to determine the feasibility and characteristics of sealing the void between adjoining ceramic tiles with a specially developed grout material having an impermeable enamel surface glaze. A two-stage process has been developed using a new grout material which consists of two distinct components: an amalgamated compound substrate and a glazed enamel surface; the amalgamated compound seal providing a tough, heat resistant bulk substrate, whilst the enamel provides an impervious surface. HPDL processing has resulted in crack free seals produced in normal atmospheric conditions. The basic process phenomena are investigated and the laser effects in terms of seal morphology, composition and microstructure are presented. Also, the resultant heat affects are analysed and described, as well as the effects of the shield gases, O 2 and Ar, during laser processing. Tiles were successfully sealed with power densities as low as 500 W/cm 2 and at rates up to 600 mm/min. Contact angle measurements revealed that due to the wettability characteristics of the amalgamated oxide compound grout (AOCG), laser surface treatment was necessary in order to alter the surface from a polycrystalline to a semi-amorphous structure, thus allowing the enamel to adhere. Bonding of the enamel to the AOCG and the ceramic tiles was identified as being principally due to van der Waals forces, and on a very small scale, some of the base AOCG material dissolving into the glaze.
Use of fly-ash slurry in backfill grouting in coal mines.
Jiang, Ning; Zhao, Jinhai; Sun, Xizhen; Bai, Liyang; Wang, Changxiang
2017-11-01
Cave backfill grouting implies grouting of the caving rock mass prior to it being compacted. The filling materials strengthen the caving rock and support the overlying strata to achieve the purpose of slowing down the surface subsidence. The broken roof will fail and collapse during mining operations performed without appropriate supporting measures being taken. It is difficult to perform continuous backfill mining on the working face of such roofs using the existing mining technology. In order to solve the above problems, fly ash and mine water are considered as filling materials, and flow characteristics of fly-ash slurry are investigated through laboratory experiments and theoretical analyses. Laws governing the diffusion of fly-ash slurry in the void of caving rock masses and in the void between a caving rock mass and a basic roof are obtained and verified. Based on the results obtained from the above analyses and actual conditions at the Zhaoguan coal mine, Shandong Province, China, a cave backfill grouting system of the hauling pipeline is developed and successfully tested at the 1703 working face in the Zhaoguan coal mine. The results demonstrate that a filling rate of 43.46% is achieved, and the surface subsidence coefficient of the grouting process is found to be 0.475. Compared to the total caving method, the proposed system is found to achieve a reduction rate of 40.63%. This effectively helps in lowering the value of the surface subsidence coefficient. Fly ash and mine water, considered as primary materials in this study, also play a significant role in improving the air quality and water environment.
Goffeng, Lars Ole; Kjuus, Helge; Heier, Mona Skard; Alvestrand, Monica; Ulvestad, Bente; Skaug, Vidar
2008-01-01
The aim of the study was to examine possible persisting visual system effects in tunnel workers previously exposed to acrylamide and N-methylolacrylamide during grouting work. Visual field light sensitivity threshold and colour vision has been examined among 44 tunnel workers 2-10 years after exposure to acrylamide and N-methylolacrylamide containing grouting agents. Forty-four tunnel workers not involved in grouting operations served as control group. Information on exposure and background variables was obtained for all participants from a questionnaire. Visual light sensitivity threshold was measured using Humphrey Visual Field Static Perimeter 740, program 30-2 Fastpack, with red stimuli on white background, and colour vision, using Lanthony D-15 Desaturated Color test. Based on D-15d test results, colour confusion index (CCI), and a severity index (C-index) was calculated. The exposed group had a significantly higher threshold for detecting single stimuli in all parts of the inner 30 degrees of the visual field compared to the control group. The foveal threshold group difference was 1.4 dB (p=0.002) (mean value, both eyes). On the Lanthony 15 Hue Desaturated test, the exposed subjects made more errors in sorting blue colours, and a statistically significant increase in C-index was observed. Surrogate measures for duration and intensity of exposure gave no further improvement of the model. The results indicate slightly reduced light sensitivity and reduced colour discrimination among the exposed subjects compared to the controls. The findings may be due to previous exposure to acrylamide containing grouts among the tunnel workers.
Tan, Daoyong; Yuan, Peng; Annabi-Bergaya, Faïza; Liu, Dong; He, Hongping
2015-01-01
Methoxy-modified kaolinite was used as a novel carrier for loading and release of the herbicide 3-amino-1,2,4-triazole, known as amitrole (abbreviated here as AMT). The methoxy modification made the interlayer space of the kaolinite available for AMT intercalation. The AMT loading content in methoxy-modified kaolinite reached up to 20.8 mass% (twice the loading content by unmodified kaolinite). About 48% of this amount is located in the interlayer space. The release profiles of the AMT fit with the modified Korsmeyer-Peppas model. Due to the diffusional restriction of the intercalated AMT by the lamellar structure of the kaolinite and the strong electrostatic attraction between the intercalated AMT and the kaolinite, a slow release of AMT from the methoxy-modified kaolinite was achieved. These results show that the methoxy-modification is a facile method to make the interlayer space of kaolinite available for hosting other guest molecules. The methoxy-modified kaolinite is a promising candidate for high-capacity loading and controlled-release of other molecules such as drugs, agrochemicals, and biochemicals. PMID:25747124
Influence of kaolinite on chiral hydrolysis of methyl dichlorprop enantiomers*
Fang, Zhao-hua; Wen, Yue-zhong; Liu, Wei-ping
2005-01-01
The effect of kaolinite on the enzymatic chiral hydrolysis of methyl dichlorprop enantiomers ((R,S)-methyl-2-(2,4-dichlorophenoxy) propanoic acid, 2,4-DPM) was investigated using chiral gas chromatography. Compared with the control without kaolinite, the enantiomeric ratio (ER) increased from 1.35 to 8.33 and the residual ratio of 2,4-DPM decreased from 60.89% to 41.55% in the presence of kaolinite. Kaolinite likely had emotion influence on lipase activity and its enantioselectivity. Moreover, the amount of kaolinite added was also found to be a sensitive factor affecting the enantioselective hydrolysis of 2,4-DPM. Fourier transform infrared (FTIR) spectroscopy studies of the interaction of lipase with kaolinite provided insight into the molecular structure of the complex and offered explanation of the effects of kaolinite on enzymatic hydrolysis of 2,4-DPM. Spectra showed that the effect of kaolinite on the hydrolysis of 2,4-DPM was affected by adsorption of lipase on kaolinite and changes of adsorbed lipase conformation, which led to the modified enantioselectivity. PMID:16187418
NASA Astrophysics Data System (ADS)
Tan, Daoyong; Yuan, Peng; Annabi-Bergaya, Faïza; Liu, Dong; He, Hongping
2015-03-01
Methoxy-modified kaolinite was used as a novel carrier for loading and release of the herbicide 3-amino-1,2,4-triazole, known as amitrole (abbreviated here as AMT). The methoxy modification made the interlayer space of the kaolinite available for AMT intercalation. The AMT loading content in methoxy-modified kaolinite reached up to 20.8 mass% (twice the loading content by unmodified kaolinite). About 48% of this amount is located in the interlayer space. The release profiles of the AMT fit with the modified Korsmeyer-Peppas model. Due to the diffusional restriction of the intercalated AMT by the lamellar structure of the kaolinite and the strong electrostatic attraction between the intercalated AMT and the kaolinite, a slow release of AMT from the methoxy-modified kaolinite was achieved. These results show that the methoxy-modification is a facile method to make the interlayer space of kaolinite available for hosting other guest molecules. The methoxy-modified kaolinite is a promising candidate for high-capacity loading and controlled-release of other molecules such as drugs, agrochemicals, and biochemicals.
Detellier, Christian
2017-01-01
Functionalization of the kaolinite (K) interlayer space is challenging. In this work, a new kaolinite-based nanohybridmaterial (K-NI) was successfully synthesized by grafting on the interlayer aluminol surfaces the ionic liquid, 1-(1-methylnaphthyl)-3-(2-hydroxyethyl) imidazolium chloride (NI), using a guest displacement strategy. A substantial increase of the basal spacing (10.8 Å) was obtained. This is a grafted derivative of kaolinite possessing one of the largest d-values. Washing in water for several days and other vigorous treatments such as sonication showed a minor effect on the integrity of the material. FTIR and 13C NMR confirmed the conservation of the structure of the ionic liquid after the grafting. Thermal analysis confirmed the presence of grafted material and was used to estimate the abundance of the grafted ionic liquid (0.44 mole per mole of kaolinite structural formula, (Al2Si2O5(OH)4)). By using cyclic voltammetry, the permeability of a film of K-NI for the bulky ferricyanide ions was demonstrated. The accumulation of nitrophenolate anions was effective (maximum capacity of 190 μmol/g), but was less important than what was expected due to the steric hindrance of the bulky grafted NI. Although the presence of chloride anions reduced the adsorption capacity, the affinity of the modified kaolinite interlayer space for the nitrophenolate anions was demonstrated. PMID:28850087
Kenne Dedzo, Gustave; Detellier, Christian
2017-08-29
Functionalization of the kaolinite (K) interlayer space is challenging. In this work, a new kaolinite-based nanohybridmaterial (K-NI) was successfully synthesized by grafting on the interlayer aluminol surfaces the ionic liquid, 1-(1-methylnaphthyl)-3-(2-hydroxyethyl) imidazolium chloride (NI), using a guest displacement strategy. A substantial increase of the basal spacing (10.8 Å) was obtained. This is a grafted derivative of kaolinite possessing one of the largest d -values. Washing in water for several days and other vigorous treatments such as sonication showed a minor effect on the integrity of the material. FTIR and 13 C NMR confirmed the conservation of the structure of the ionic liquid after the grafting. Thermal analysis confirmed the presence of grafted material and was used to estimate the abundance of the grafted ionic liquid (0.44 mole per mole of kaolinite structural formula, (Al₂Si₂O₅(OH)₄)). By using cyclic voltammetry, the permeability of a film of K-NI for the bulky ferricyanide ions was demonstrated. The accumulation of nitrophenolate anions was effective (maximum capacity of 190 μmol/g), but was less important than what was expected due to the steric hindrance of the bulky grafted NI. Although the presence of chloride anions reduced the adsorption capacity, the affinity of the modified kaolinite interlayer space for the nitrophenolate anions was demonstrated.
NASA Astrophysics Data System (ADS)
Høien, Are Håvard; Nilsen, Bjørn
2014-05-01
The Løren road tunnel is a part of a major project at Ring road 3 in Oslo, Norway. The rock part of the tunnel is 915 m long and has two tubes with three lanes and breakdown lanes. Strict water ingress restriction was specified and continuous rock mass grouting was, therefore, carried out for the entire tunnel, which was excavated in folded Cambro-Silurian shales intruded by numerous dykes. This paper describes the rock mass grouting that was carried out for the Løren tunnel. Particular emphasis is placed on discussing grout consumption and the challenges that were encountered when passing under a distinct rock depression. Measurement while drilling (MWD) technology was used for this project, and, in this paper, the relationships between the drill parameter interpretation (DPI) factors water and fracturing are examined in relation to grout volumes. A lowering of the groundwater table was experienced during excavation under the rock depression, but the groundwater was nearly re-established after completion of the main construction work. A planned 80-m watertight concrete lining was not required to be built due to the excellent results from grouting in the rock depression area. A relationship was found between leakages mapped in the tunnel and the DPI water factor, indicating that water is actually present where the DPI water factor shows water in the rock. It is concluded that, for the Løren tunnel, careful planning and high-quality execution of the rock mass grouting made the measured water ingress meet the restrictions. For future projects, the DPI water factor may be used to give a better understanding of the material in which the rock mass grouting is performed and may also be used to reduce the time spent and volumes used when grouting.
Disinfection of water with new chitosan-modified hybrid clay composite adsorbent.
Unuabonah, Emmanuel I; Adewuyi, Adewale; Kolawole, Matthew O; Omorogie, Martins O; Olatunde, Olalekan C; Fayemi, Scott O; Günter, Christina; Okoli, Chukwunonso P; Agunbiade, Foluso O; Taubert, Andreas
2017-08-01
Hybrid clay composites were prepared from Kaolinite clay and Carica papaya seeds via modification with chitosan, Alum, NaOH, and ZnCl 2 in different ratios, using solvothermal and surface modification techniques. Several composite adsorbents were prepared, and the most efficient of them for the removal of gram negative enteric bacteria was the hybrid clay composite that was surface-modified with chitosan, Ch-nHYCA 1:5 (Chitosan: nHYCA = 1:5). This composite adsorbent had a maximum adsorption removal value of 4.07 × 10 6 cfu/mL for V. cholerae after 120 min, 1.95 × 10 6 cfu/mL for E. coli after ∼180 min and 3.25 × 10 6 cfu/mL for S. typhi after 270 min. The Brouers-Sotolongo model was found to better predict the maximum adsorption capacity ( q max ) of Ch-nHYCA 1:5 composite adsorbent for the removal of E. coli with a q max of 103.07 mg/g (7.93 × 10 7 cfu/mL) and V. cholerae with a q max of 154.18 mg/g (1.19 × 10 8 cfu/mL) while the Sips model best described S. typhi adsorption by Ch-nHYCA 1:5 composite with an estimated q max of 83.65 mg/g (6.43 × 10 7 cfu/mL). These efficiencies do far exceed the alert/action levels of ca. 500 cfu/mL in drinking water for these bacteria. The simplicity of the composite preparation process and the availability of raw materials used for its preparation underscore the potential of this low-cost chitosan-modified composite adsorbent (Ch-nHYCA 1:5 ) for water treatment.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Ethridge, F.G.; Saracino, A.M.; Burns, L.K.
The encompassing sandstones, siltstones, shales and thin conglomerates of the gasified G Coal seam at the North Knobs SDB-UCG site were deposited mainly in fluvial and poorly-drained swamp environments. These beds dip at 65/sup 0/ at the North Knobs site. Thin section and SEM analyses of the sandstones and coarse siltstones show that they are sublithic to subarkosic arenites cemented with clay minerals, calcite hematite, siderite and silica. The sandstones of Unit D directly above the coal seam have the highest concentration of calcite cement, the lowest mean grain size, and are best sorted in terms of quartz grain sizemore » variations; however, they are the worst sorted in terms of sieve size variations. Clay minerals in the sandstones are dominantly kaolinite and smectite with lesser amounts of illite and chlorite. These clays are of secondary origin. Heat alteration is present only in coals and overburden rock from cores that penetrated the cavity. Thermally altered rocks including hornfels, buchite, paralava rock and paralava breccia were found in the bottom of the dipping cavity near the injection well. The high temperature minerals of tridymite, cristobalite, mullite, cordierite, monoclinic pyroxene and high temperature plagioclase indicate that temperatures of at least 1200/sup 0/C to 1400/sup 0/C were attained in the lower part of the burn cavity. The mechanical test on the unaltered and altered overburden rock show that the most important lithologic property controlling rock strength and seismic wave velocity is the amount and type of cement in the rock. Other parameters measured were grain size, amount of clay cement, and porosity; sorting had a secondary effect on the rock strength and seismic wave velocity. There is a non-linear and direct relationship between mechanical strength and ultrasonic wave velocities for the rock tests. 30 references.« less
The spectroscopic study of building composites containing natural sorbents.
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.
Pedogenesis of a catena of the Farmdale-Sangamon Geosol complex in the north central United States
Jacobs, P.M.; Konen, M.E.; Curry, B. Brandon
2009-01-01
The Farmdale-Sangamon Geosol pedocomplex consists of the Sangamon Geosol and the overlying Farmdale Geosol, which form the most extensive terrestrial record of the last interglacial to glacial transition in the Midwest United States. The geosol complex formed for upwards of 100??ka, extending from the end of MIS 6 through 4 for the Sangamon Geosol, then the Farmdale Geosol for during a brief episode at the end of MIS 3 following slow accumulation and pedogenic modification of eolian silt deposited on top of the Sangamon Geosol. Our study site consists of a buried paleo-hillslope transect that forms a catena, enabling evaluation of slope effects on interglacial-scale soil formation. The Sangamon Geosol is formed in calcareous and illitic glaciogenic sediment. Along the catena the Sangamon Geosol profiles display some morphological changes, namely in terms of colors that we interpret as indicators of differences in drainage. Most thickness and horizonation characteristics are similar all along the transect, with intact upper sola horizons (AE and E horizons) that overlie clay-enriched Bt horizons. The Bt horizons contain abundant clay that exists as illuvial clay coatings, matrix infills, and as mosaic-speckled domains. The clay originated both by in situ weathering and through illuviation from the clay depleted upper sola. Slope does not appear to affect Bt characteristics beyond redder hues of the matrix and clay coatings in the upper slope position. With depth, effects of carbonate leaching and infilling of clay in the matrix decrease and clay coatings are restricted to walls of voids adjacent to aggregates. Clay mineralogy shows illite depletion, but no interstratified kaolinite-expandable minerals, indicating the degree of weathering is not as great as is typical of Sangamon Geosol profiles formed in loess or in glaciogenic sediment of the central Illinois type area. Clay mineralogy is also stratified with depth, coincident with particle size, which probably indicates sorting of layers of illitic dolomite and shale. Variation of horizon and profile characteristics appears to largely be a function of particle size variability and stratification than topographic position in the catena. The influence of hillslope position on soil redistribution during formation of the Sangamon Geosol appears negligible given the uniformity of upper solum horizon thickness and sandy particle size characteristics, so we conclude that a bioturbation and rainwash origin of the upper solum and the texture contrast in these profiles is not the best process model explanation. We suggest that the base-rich nature of these soils led to ecosystem characteristics that discouraged erosion and encouraged infiltration and a lessivage-type origin of the texture contrast. No convincing evidence of MIS 6 through MIS 4 loess occurs at this site. The Farmdale Geosol formed in the Robein Silt, which is Roxana Silt (MIS 3 loess) that was redistributed downslope. The Robein Silt is thicker and finer in the topographic low and indicates the cooler and forested environmental conditions during MIS 3 were conducive to downslope movement of soil and also produced greater differences in drainage-induced soil morphological changes in the Farmdale Geosol. ?? 2009 Elsevier B.V. All rights reserved.
Koarashi, Jun; Nishimura, Syusaku; Atarashi-Andoh, Mariko; Matsunaga, Takeshi; Sato, Tsutomu; Nagao, Seiya
2018-08-01
The Fukushima Daiichi nuclear power plant accident caused serious radiocesium ( 137 Cs) contamination in soils in a range of terrestrial ecosystems. It is well documented that the interaction of 137 Cs with soil constituents, particularly clay minerals, in surface soil layers exerts strong control on the behavior of this radionuclide in the environment; however, there is little understanding of how soil aggregation-the binding of soil particles together into aggregates-can affect the mobility and bioavailability of 137 Cs in soils. To explore this, soil samples were collected at seven sites under different land-use conditions in Fukushima and were separated into four aggregate-size fractions: clay-sized (<2 μm); silt-sized (2-20 μm); sand-sized (20-212 μm); and macroaggregates (212-2000 μm). The fractions were then analyzed for 137 Cs content and extractability and mineral composition. In forest soils, aggregate formation was significant, and 69%-83% of 137 Cs was associated with macroaggregates and sand-sized aggregates. In contrast, there was less aggregation in agricultural field soils, and approximately 80% of 137 Cs was in the clay- and silt-sized fractions. Across all sites, the 137 Cs extractability was higher in the sand-sized aggregate fractions than in the clay-sized fractions. Mineralogical analysis showed that, in most soils, clay minerals (vermiculite and kaolinite) were present even in the larger-sized aggregate fractions. These results demonstrate that larger-sized aggregates are a significant reservoir of potentially mobile and bioavailable 137 Cs in organic-rich (forest and orchard) soils. Our study suggests that soil aggregation reduces the mobility of particle-associated 137 Cs through erosion and resuspension and also enhances the bioavailability of 137 Cs in soils. Copyright © 2018 Elsevier Ltd. All rights reserved.
The Global ASTER Geoscience and Mineralogical Maps
NASA Astrophysics Data System (ADS)
Abrams, M.
2017-12-01
In 2012, Australia's Commonwealth Scientific and Industrial Research Organization (CSIRO) released 17 Geoscience mineral maps for the continent of Australia We are producing the CSIRO Geoscience data products for the entire land surface of the Earth. These maps are created from Advanced Spacecraft Thermal Emission and Reflection Radiometer (ASTER) data, acquired between 2000 and 2008. ASTER, onboard the United States' Terra satellite, is part of NASA's Earth Observing System. This multispectral satellite system has 14 spectral bands spanning: the visible and near-infrared (VNIR) @ 15 m pixel resolution; shortwave-infrared (SWIR) @ 30 m pixel resolution; and thermal infrared (TIR) @ 90 m pixel resolution. In a polar-orbit, ASTER acquires a 60 km swath of data.The CSIRO maps are the first continental-scale mineral maps generated from an imaging satellite designed to measure clays, quartz and other minerals. Besides their obvious use in resource exploration, the data have applicability to climatological studies. Over Australia, these satellite mineral maps improved our understanding of weathering, erosional and depositional processes in the context of changing weather, climate and tectonics. The clay composition map showed how kaolinite has developed over tectonically stable continental crust in response to deep weathering. The same clay composition map, in combination with one sensitive to water content, enabled the discrimination of illite from montmorillonite clays that typically develop in large depositional environments over thin (sinking) continental crust. This product was also used to measure temporal gains/losses of surface clay caused by periodic wind erosion (dust) and rainfall inundation (flood) events. The two-year project is undertaken by JPL with collaboration from CSIRO. JPL has in-house the entire ASTER global archive of Level 1B image data—more than 1,500,000 scenes. This cloud-screened and vegetation-masked data set will be the basis for creation of the suite of global Geoscience products using all of ASTER's 14 VNIR-SWIR-TIR spectral bands resampled to 100 m pixel resolution. We plan a staged release of the geoscience products through NASA's LPDAAC.
Fines migration during CO 2 injection: Experimental results interpreted using surface forces
DOE Office of Scientific and Technical Information (OSTI.GOV)
Xie, Quan; Saeedi, Ali; Delle Piane, Claudio
The South West Hub project is one of the Australian Flagship Carbon Capture and Storage projects located in the south-west of Western Australia. To evaluate the injectivity potential during the forthcoming full-scale CO 2 injection, we conducted three core-flooding experiments using reservoir core plugs from the well Harvey-1. We aimed to investigate in this paper whether the injection of CO 2 leads to fines migration and permeability reduction due to the relatively high kaolinite content (up to 13%) in the injection interval of the target formation (i.e. the Wonnerup Member of the Lesueur Formation). We imaged the core samples beforemore » flooding to verify the presence of kaolinite at the pore-scale using scanning electron microscopy (SEM). We also examined the pore network of the core plugs before and after the core-flooding experiments using Nuclear Magnetic Resonance (NMR). Moreover, to gain a better understanding of any kaolinite fines migration, we delineated surface force using two models based on Derjaguin-Landau-Verwey-Overbeek (denoted by DLVO) theory coupled hydrodynamic force: (1) sphere/flat model representing interaction between kaolinite/quartz, and (2) flat/flat model representing interaction between kaolinite/kaolinite. Our core-flooding experimental results showed that CO 2/brine injection triggered moderate to significant reduction in the permeability of the core samples with a negligible porosity change. NMR measurements supported the core-flooding results, suggesting that the relatively large pores disappeared in favour of a higher proportion of the medium to small pores after flooding. The DLVO calculations showed that some kaolinite particles probably lifted off and detached from neighbouring kaolinite particles rather than quartz grains. Moreover, the modelling results showed that the kaolinite fines migration would not occur under normal reservoir multiphase flow conditions. This is not because of the low hydrodynamic force. It is rather because the geometries of the particles dominate their interplay. Finally and overall, both of the experimental and analytical modelling results point to the fines migration to be the most likely cause of the permeability impairment observed during core-flooding experiments.« less
Fines migration during CO 2 injection: Experimental results interpreted using surface forces
Xie, Quan; Saeedi, Ali; Delle Piane, Claudio; ...
2017-09-04
The South West Hub project is one of the Australian Flagship Carbon Capture and Storage projects located in the south-west of Western Australia. To evaluate the injectivity potential during the forthcoming full-scale CO 2 injection, we conducted three core-flooding experiments using reservoir core plugs from the well Harvey-1. We aimed to investigate in this paper whether the injection of CO 2 leads to fines migration and permeability reduction due to the relatively high kaolinite content (up to 13%) in the injection interval of the target formation (i.e. the Wonnerup Member of the Lesueur Formation). We imaged the core samples beforemore » flooding to verify the presence of kaolinite at the pore-scale using scanning electron microscopy (SEM). We also examined the pore network of the core plugs before and after the core-flooding experiments using Nuclear Magnetic Resonance (NMR). Moreover, to gain a better understanding of any kaolinite fines migration, we delineated surface force using two models based on Derjaguin-Landau-Verwey-Overbeek (denoted by DLVO) theory coupled hydrodynamic force: (1) sphere/flat model representing interaction between kaolinite/quartz, and (2) flat/flat model representing interaction between kaolinite/kaolinite. Our core-flooding experimental results showed that CO 2/brine injection triggered moderate to significant reduction in the permeability of the core samples with a negligible porosity change. NMR measurements supported the core-flooding results, suggesting that the relatively large pores disappeared in favour of a higher proportion of the medium to small pores after flooding. The DLVO calculations showed that some kaolinite particles probably lifted off and detached from neighbouring kaolinite particles rather than quartz grains. Moreover, the modelling results showed that the kaolinite fines migration would not occur under normal reservoir multiphase flow conditions. This is not because of the low hydrodynamic force. It is rather because the geometries of the particles dominate their interplay. Finally and overall, both of the experimental and analytical modelling results point to the fines migration to be the most likely cause of the permeability impairment observed during core-flooding experiments.« less
DOE Office of Scientific and Technical Information (OSTI.GOV)
Pickenheim, B.; Hansen, E.; Leishear, R.
A 10-inch READCO mixer is used for mixing the premix (45 (wt%) fly ash, 45 wt% slag, and 10 wt% portland cement) with salt solution in the Saltstone Production Facility (SPF). The Saltstone grout free falls into the grout hopper which feeds the suction line leading to the Watson SPX 100 duplex hose pump. The Watson SPX 100 pumps the grout through approximately 1500 feet of piping prior to being discharged into the Saltstone Disposal Facility (SDF) vaults. The existing grout hopper has been identified by the Saltstone Enhanced Low Activity Waste Disposal (ELAWD) project for re-design. The current nominalmore » working volume of this hopper is 12 gallons and does not permit handling an inadvertent addition of excess dry feeds. Saltstone Engineering has proposed a new hopper tank that will have a nominal working volume of 300 gallons and is agitated with a mechanical agitator. The larger volume hopper is designed to handle variability in the output of the READCO mixer and process upsets without entering set back during processing. The objectives of this task involve scaling the proposed hopper design and testing the scaled hopper for the following processing issues: (1) The effect of agitation on radar measurement. Formation of a vortex may affect the ability to accurately measure the tank level. The agitator was run at varying speeds and with varying grout viscosities to determine what parameters cause vortex formation and whether measurement accuracy is affected. (2) A dry feeds over addition. Engineering Calculating X-ESR-Z-00017 1 showed that an additional 300 pounds of dry premix added to a 300 gallon working volume would lower the water to premix ratio (W/P) from the nominal 0.60 to 0.53 based on a Salt Waste Processing Facility (SWPF) salt simulant. A grout with a W/P of 0.53 represents the upper bound of grout rheology that could be processed at the facility. A scaled amount of dry feeds will be added into the hopper to verify that this is a recoverable situation. (3) The necessity of baffles in the hopper. The preference of the facility is not to have baffles in the hopper; however, if the initial testing indicates inadequate agitation or difficulties with the radar measurement, baffles will be tested.« less
Kaolinite adsorption-regeneration system for dyestuff treatment by Fenton based processes.
Rosales, Emilio; Anasie, Delia; Pazos, Marta; Lazar, Iuliana; Sanromán, M Angeles
2018-05-01
The regeneration and reuse of adsorbents is a subject of interest nowadays in order to reduce the pollution and the wastes generated in the adsorption wastewater treatment. In this work, the regeneration of the spent kaolinite by different advanced oxidation processes (Fenton, electro-Fenton and electrokinetic-Fenton) was evaluated. Initially, it was confirmed the ability of a low cost clayey material, kaolinite, for the adsorption of model dye such as Rhodamine B showing Freundlich isotherm fitting. Then, the regeneration and consequent degradation of the pollutant in the adsorbent by Fenton based processes was carried out. The role of different parameters affecting the regeneration process (H 2 O 2 :Fe 2+ ratio, liquid:solid ratio) were evaluated. Working at 100:1 H 2 O 2 :Fe 2+ ratio and 30min near complete dye removal (around 97%) from kaolinite was obtained by Fenton treatment. After that, a two-stage treatment for adsorption-regeneration was evaluated during five treatment cycles demonstrating its viability for regeneration of the adsorbent through dye degradation. Based on the successful application of Fenton technique, the improvement of the treatment by electro-Fenton and electrokinetic-Fenton were studied for different solid:liquid ratios achieving satisfactory regeneration values. Copyright © 2017 Elsevier B.V. All rights reserved.
Experimental observation of standing interfacial waves induced by surface waves in muddy water
NASA Astrophysics Data System (ADS)
Maxeiner, Eric; Dalrymple, Robert A.
2011-09-01
A striking feature has been observed in a laboratory wave tank with a thin layer of clear water overlying a layer of mud. A piston-type wave maker is used to generate long monochromatic surface waves in a tank with a layer of kaolinite clay at the bottom. The wave action on the mud causes the clay particles to rise from the bottom into the water column, forming a lutocline. As the lutocline approaches the water surface, a set of standing interfacial waves form on the lutocline. The interfacial wave directions are oriented nearly orthogonal to the surface wave direction. The interfacial waves, which sometimes cover the entire length and width of the tank, are also temporally subharmonic as the phase of the interfacial wave alternates with each passing surface wave crest. These interfacial waves are the result of a resonant three-wave interaction involving the surface wave train and the two interfacial wave trains. The interfacial waves are only present when the lutocline is about 3 cm of the water surface and they can be sufficiently nonlinear as to exhibit superharmonics and a breaking-type of instability.
Enrofloxacin sorption on smectite clays: effects of pH, cations, and humic acid.
Yan, Wei; Hu, Shan; Jing, Chuanyong
2012-04-15
Enrofloxacin (ENR) occurs widely in natural waters because of its extensive use as a veterinary chemotherapeutic agent. To improve our understanding of the interaction of this emerging contaminant with soils and sediments, sorption of ENR on homoionic smectites and kaolinite was studied as a function of pH, ionic strength, exchangeable cations, and humic acid concentration. Batch experiments and in situ ATR-FTIR analysis suggested multiple sorption mechanisms. Cation exchange was a major contributor to the sorption of cationic ENR species on smectite. The decreased ENR sorption with increasing ionic strength indicated the formation of outer-sphere complexes. Exchangeable cations significantly influenced the sorption capacity, and the observed order was Cs
NASA Astrophysics Data System (ADS)
Azhar, A. T. S.; Jefferson, I.; Madun, A.; Abidin, M. H. Z.; Rogers, C. D. F.
2018-04-01
Electrokinetic stabilisation (EKS) method has the ability to solve the problems of soft highly compressibility soil. This study will present the results from an experimental study of EKS on soft soils using inactive kaolinite clay, inert electrode and distilled water (DW) as a pure system mechanism before any chemical stabilisers being used in this research. Therefore, this will provide a baseline study to improve the efficiency of EKS approach. The test model was using inert electrode of Electrokinetic Geosythentic (EKG) developed at the Newcastle University to apply a constant voltage gradient of 50 V/m across a soil sample approximately 400 mm. Distilled water was used at the pore electrolyte fluid compartments supplied under zero hydraulic gradient conditions for the periods of 3, 7 and 14 days. Throughout the monitoring, physical and chemical characteristics were measured. Results from the monitoring data, physical and chemical properties of the pure system showed the development of pH gradient, the changes of electrical conductivity and chemical concentrations with regards to the distance from anode and treatment periods due to the electrochemical effects even though there was no chemical stabilisers were introduced or released from the degradation of electrodes.
NASA Astrophysics Data System (ADS)
Kaplan, Hannah H.; Milliken, Ralph E.; Fernández-Remolar, David; Amils, Ricardo; Robertson, Kevin; Knoll, Andrew H.
2016-09-01
Outcrops of hydrated minerals are widespread across the surface of Mars, with clay minerals and sulfates being commonly identified phases. Orbitally-based reflectance spectra are often used to classify these hydrated components in terms of a single mineralogy, although most surfaces likely contain multiple minerals that have the potential to record local geochemical conditions and processes. Reflectance spectra for previously identified deposits in Ius and Melas Chasma within the Valles Marineris, Mars, exhibit an enigmatic feature with two distinct absorptions between 2.2 and 2.3 μm. This spectral 'doublet' feature is proposed to result from a mixture of hydrated minerals, although the identity of the minerals has remained ambiguous. Here we demonstrate that similar spectral doublet features are observed in airborne, field, and laboratory reflectance spectra of rock and sediment samples from Rio Tinto, Spain. Combined visible-near infrared reflectance spectra and X-ray diffraction measurements of these samples reveal that the doublet feature arises from a mixture of Al-phyllosilicate (illite or muscovite) and jarosite. Analyses of orbital data from the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) shows that the martian spectral equivalents are also consistent with mixtures of Al-phyllosilicates and jarosite, where the Al-phyllosilicate may also include kaolinite and/or halloysite. A case study for a region within Ius Chasma demonstrates that the relative proportions of the Al-phyllosilicate(s) and jarosite vary within one stratigraphic unit as well as between stratigraphic units. The former observation suggests that the jarosite may be a diagenetic (authigenic) product and thus indicative of local pH and redox conditions, whereas the latter observation may be consistent with variations in sediment flux and/or fluid chemistry during sediment deposition.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Zeitler, T. R.; Greathouse, J. A.; Cygan, R. T.
Low-salinity water flooding, a method of enhanced oil recovery, consists of injecting low ionic strength fluids into an oil reservoir in order to detach oil from mineral surfaces in the underlying formation. Although highly successful in practice, the approach is not completely understood at the molecular scale. Molecular dynamics simulations have been used to investigate the effect of surface protonation on the adsorption of an anionic crude oil component on clay mineral edge surfaces. A set of interatomic potentials appropriate for edge simulations has been applied to the kaolinite (010) surface in contact with an aqueous nanopore. Decahydro-2-napthoic acid inmore » its deprotonated form (DHNA –) was used as a representative resin component of crude oil, with monovalent and divalent counterions, to test the observed trends in low-salinity water flooding experiments. Surface models include fully protonated (neutral) and deprotonated (negative) edge sites, which require implementation of a new deprotonation scheme. The surface adsorptive properties of the kaolinite edge under neutral and deprotonated conditions have been investigated for low and high DHNA – concentrations with Na + and Ca 2+ as counterions. The tendency of DHNA – ions to coordinate with divalent (Ca 2+) rather than monovalent (Na +) ions greatly influences adsorption tendencies of the anion. Additionally, the formation of net positively charged surface sites due to Ca 2+ at deprotonated sites results in increased DHNA – adsorption. Divalent cations such as Ca 2+ are able to efficiently bridge surface sites and organic anions. Replacing those cations with monovalent cations such as Na + diminishes the bridging mechanism, resulting in reduced adsorption of the organic species. As a result, a clear trend of decreased DHNA – adsorption is observed in the simulations as Ca 2+ is replaced by Na + for deprotonated surfaces, as would be expected for oil detachment from reservoir formations following a low-salinity flooding event.« less
Zeitler, T. R.; Greathouse, J. A.; Cygan, R. T.; ...
2017-10-05
Low-salinity water flooding, a method of enhanced oil recovery, consists of injecting low ionic strength fluids into an oil reservoir in order to detach oil from mineral surfaces in the underlying formation. Although highly successful in practice, the approach is not completely understood at the molecular scale. Molecular dynamics simulations have been used to investigate the effect of surface protonation on the adsorption of an anionic crude oil component on clay mineral edge surfaces. A set of interatomic potentials appropriate for edge simulations has been applied to the kaolinite (010) surface in contact with an aqueous nanopore. Decahydro-2-napthoic acid inmore » its deprotonated form (DHNA –) was used as a representative resin component of crude oil, with monovalent and divalent counterions, to test the observed trends in low-salinity water flooding experiments. Surface models include fully protonated (neutral) and deprotonated (negative) edge sites, which require implementation of a new deprotonation scheme. The surface adsorptive properties of the kaolinite edge under neutral and deprotonated conditions have been investigated for low and high DHNA – concentrations with Na + and Ca 2+ as counterions. The tendency of DHNA – ions to coordinate with divalent (Ca 2+) rather than monovalent (Na +) ions greatly influences adsorption tendencies of the anion. Additionally, the formation of net positively charged surface sites due to Ca 2+ at deprotonated sites results in increased DHNA – adsorption. Divalent cations such as Ca 2+ are able to efficiently bridge surface sites and organic anions. Replacing those cations with monovalent cations such as Na + diminishes the bridging mechanism, resulting in reduced adsorption of the organic species. As a result, a clear trend of decreased DHNA – adsorption is observed in the simulations as Ca 2+ is replaced by Na + for deprotonated surfaces, as would be expected for oil detachment from reservoir formations following a low-salinity flooding event.« less
NASA Astrophysics Data System (ADS)
Scott, M.; Verba, C.; Falcon, A.; Poston, J.; McKoy, M.
2017-12-01
Because of their multiple uses in clean energy technologies, rare earth elements (REE) are critical for national economic and energy security. With no current domestic source, supply remains a major concern for domestic security. Underclay - specifically the layer of stratum beneath a coal bed - is a potentially rich source of REE. This study focuses on the characterization and ion exchange recovery of REE from underclay samples from the Lower Freeport, Middle Kittanning, and Pittsburgh coal seams in West Virginia. Multimodal techniques provided quantitative assessments of REE-bearing mineral phases in select underclays and the influence of organic acid rock treatment on the recovery of REE from both exchangeable and crystalline mineral phases present. All samples are from extensively weathered horizons that contain abundant kaolinite and illite. Total REE concentrations range from 250-450 ppm and all samples have a HREE/LEEE ratio >20%. Rare earth element bearing minerals identified in the clay are monazite, xenotime, florencite, and crandallite. Our selective recovery approach is designed to isolate and recover REE through partial dissolution of the clay matrix and ion exchange rather than dissolution/recovery of phosphate or aluminosilicate bound REE. These results provide a better understanding of coal seam underclay, the affinity of REEs for specific ligands and colloids, and how the rock and ligands respond to different chemical treatments. These processes are important to the development and commercialization of efficient and cost effective methods to extract REE from domestic geologic deposits and recover into salable forms.
Evaluation of PCDD/Fs emissions during ceramic production: a laboratory study.
Lu, Mang; Luo, Yi-Jing; Zhang, Zhong-Zhi; Xiao, Meng; Zhang, Min
2012-08-30
Because of the ubiquity of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in kaolinitic clays, the ceramic industry is considered to be a potential source of PCDD/Fs. However, studies on the emission of PCDD/Fs from ceramic production are still very scarce. In this study, PCDD/Fs emissions during ceramic production were investigated in an electric laboratory batch kiln. The results showed that the PCDD/Fs were completely removed from the ceramic pieces after 30 min of firing at the peak temperature of 1200°C. Nevertheless, on the mass and international toxic equivalent basis, 27.5% and 46.2% of the total PCDD/Fs amount in the raw clay were released into the atmosphere during firing, respectively. These PCDD/Fs were emitted into the air before the temperature was elevated to a level high enough for their destruction. Dechlorination reactions generated a broad distribution within the PCDD/Fs congeners including a variety of non-2,3,7,8-substituted ones. The emission of PCDD/Fs was decreased to 16.3 wt.% of the total PCDD/Fs amount in the raw clay, when the initial kiln temperature was enhanced to 600°C. The emission of PCDD/Fs could be reduced significantly in the presence of a glaze coating on the ceramic test piece. These results indicated that ceramic production is an un-neglectable source of PCDD/Fs in the environment. Copyright © 2012 Elsevier B.V. All rights reserved.
Geochemistry and Minerality of Wine
NASA Astrophysics Data System (ADS)
Oze, C.; Horton, T. W.; Beaman, M.
2010-12-01
Kaolinite (Al2Si2O5(OH)4) and gibbsite (Al(OH)3) are capable of forming in a variety of environments including anthropogenic solutions such as wine. Here, we evaluate the geochemistry of twelve white wines in order to assess the potential relationship between kaolinite/gibbsite saturation and minerality, a common wine descriptor used to express the rock and/or soil character in the aromas and flavors of wines. Aluminum and Si concentrations ranged from 228-1,281 µg L-1 and 6,583-19,746 µg L-1, respectively, where Si and Al are the only elements to demonstrate positive covariance with minerality scores. Sulfur levels varied from 25,013-167,383 µg L-1 and show the strongest negative covariance with minerality scores. However, like all of the elements studied (Al, Si, Na, Mg, S, K, Ca, and Fe), these trends were not significantly different than random at the 95% confidence level. In contrast, the relative degrees of gibbsite/kaolinite saturation display strong positive covariance with minerality scores and these trends are not random at the greater than 95% confidence level. Overall, our tasters were able to accurately assess the degree of gibbsite/kaolinite saturation amongst the twelve wines based on the objective of assessing minerality. Although the wines were undersaturated with respect to gibbsite/kaolinite, geochemical modeling reveals that increasing the wines’ pHs from ~3.3 to 4.1-4.6 (which is achievable on the palate where saliva has a pH of 7.4) results in gibbsite/kaolinite oversaturation. By considering that minerality is a function of gibbsite/kaolinite saturation and decreasing S, the origin of minerality’s taste and chemical origin in wine with known physical standards becomes increasingly crystalline.
Heckman, R. A.
1971-12-14
Nuclear explosions have been proposed as a means for recovering gas from underground gas-bearing rock formations. In present practice, the nuclear device is positioned at the end of a long pipe which is subsequently filled with grout or concrete. After the device is exploded, the grout is drilled through to provide a flow path for the released gas to the ground surface. As settled grout is brittle, often the compressive shock of the explosion fractures the grout and deforms the pipe so that it may not be removed nor reused. In addition, the pipe is sometimes pinched off completely and the gas flow is totally obstructed. (2 claims)
Heckman, R.A.
1971-12-14
Nuclear explosions have been proposed as a means for recovering gas from underground gas-bearing rock formations. In present practice, the nuclear device is positioned at the end of a long pipe which is subsequently filled with grout or concrete. After the device is exploded, the grout is drilled through to provide a flow path for the released gas to the ground surface. As settled grout is brittle, often the compressive shock of the explosion fractures the grout and deforms the pipe so that it may not be removed nor reused. In addition, the pipe is sometimes pinched off completely and the gas flow is totally obstructed. (2 claims)
Ahrens, Ernst H.
1999-01-01
An ultrafine cementitious grout in three particle grades containing Portland cement, pumice as a pozzolanic material and superplasticizer in the amounts of about 30 wt. % to about 70 wt. % Portland cement; from about 30 wt. % to about 70 wt. % pumice containing at least 70% amorphous silicon dioxide; and from 1.2 wt. % to about 5.0 wt. % superplasticizer. The superplasticizer is dispersed in the mixing water prior to the addition of dry grout and the W/CM ratio is about 0.4 to 1/1. The grout has very high strength and very low permeability with good workability. The ultrafine particle sizes allow for sealing of microfractures below 10 .mu.m in width.
NASA Astrophysics Data System (ADS)
Ivanova, Ekaterina
2013-04-01
The weathering of sheet silicates is well known to be related to local and global geochemical cycles. Content and composition of clay minerals in soil determine the sorption properties of the soil horizons, water-holding capacity of the soil, stickiness, plasticity, etc. Microorganisms have a diverse range of mechanisms of minerals' structure transformation (acid- and alkali formation, biosorption, complexing, etc). One of the methods is an ability of exopolysaccharide-formation, in particular the formation of mucus, common to many bacteria, including cyanobacteria. Mucous covers cyanobacteria are the specific econiches for other bacteria, including actinomycetes. The objective was to analyze the structural changes of clay minerals under the influence of the cyanobacterial-actinomycetes associative growth. The objects of the study were: 1) the experimental symbiotic association, consisting of free-living heterocyst-formative cyanobacterium Anabaena variabilis Kutz. ATCC 294132 and actinomycete Streptomyces cyaneofuscatus FR837630, 2) rock samples obtained from the Museum of the Soil Science Department of the Lomonosov Moscow State University: kaolinite, consisting of kaolin (96%) Al4 (OH) 8 [Si4O10]; mixed with hydromica, chlorite and quartz; vermiculite, consisting of vermiculite (Ca, Mg, ...)*(Mg, Fe)3(OH)2[(Si, Al)4O10]*4H2O and trioctahedral mica (biotite). The mineralogical compositions of the rocks were determined by the universal X-ray Diffractometer Carl Zeiss Yena. The operationg regime was kept constant (30 kv, 40 mA). The cultivation of the association of actinomycete S. cyanoefuscatus and cyanobacterium A. variabilis caused a reduction in the intensity of kaolinite and hydromica reflexes. However, since both (mica and kaolinite) components have a rigid structure, the significant structural transformation of the minerals was not revealed. Another pattern was observed in the experiment, where the rock sample of vermiculite was used as the mineral substrate. The associative growth of S. cyaneofuscatus and A. variabilis led to the transformation of minerals indicated by the significant decreasing of the intensity of the reflections of vermiculite as well as biotite. Reduction in the intensity of the basal reflections of vermiculite (d001, d004 and d005) three times indicates the process of biodestruction of this component of the rock. The formation of the swelling phase - the product of biotite transformation into the mica-vermicullite mixed-layer formation was revealed. The study demonstrates the differences in the transformation of clay minerals under the influence of cyanobacterial-actinomycetes association, depending on minerals' crystal chemistry and it's resistance to weathering. The rate of the process transformation of micas into the mixed-layer formation depends on their structure - trioctahedral mica (biotite, part of vermiculite sample) are transformated much faster than dioctahedral. The growth of associative thallus and monocultures of cyanobacterium and actinomycete promoted the removal of potassium (?), magnesium (Mg) and aluminum (Al) from the crystal lattice of the rock sample of vermiculite. Leaching of elements due to the influence of associative thallus exceeded the release of cations observed in the sample under the influence of the growth of cyanobacterium and streptomycete monocultures and in the control sample of vermiculite. Therefore, the association's biodegradation impact on the mineral structure was significantly greater than the influence of the monocultures of cyanobacteria and actinomycetes.
Kaolinite flocculation induced by smectite addition - a transmission X-ray microscopic study.
Zbik, Marek S; Song, Yen-Fang; Frost, Ray L
2010-09-01
The influence of smectite addition on kaolinite suspensions in water was investigated by transmission X-ray microscopy (TXM) and Scanning Electron Microscopy (SEM). Sedimentation test screening was also conducted. Micrographs were processed by the STatistic IMage Analysing (STIMAN) program and structural parameters were calculated. From the results of the sedimentation tests important influences of small smectite additions to about 3wt.% on kaolinite suspension flocculation has been found. In order to determine the reason for this smectite impact on kaolinite suspension, macroscopic behaviour micro-structural examination using Transmission X-ray Microscope (TXM) and SEM has been undertaken. TXM & SEM micrographs of freeze-dried kaolinite-smectite suspensions with up to 20% smectite showed a high degree of orientation of the fabric made of highly oriented particles and greatest density when 3wt.% of smectite was added to the 10wt.% dense kaolinite suspension. In contrast, suspensions containing pure kaolinite do not show such platelet mutual orientation but homogenous network of randomly oriented kaolinite platelets. This suggests that in kaolinite-smectite suspensions, smectite forms highly oriented basic framework into which kaolinite platelets may bond in face to face preferential contacts strengthening structure and allowing them to show plastic behaviour which is cause of platelets orientation. Copyright 2010 Elsevier Inc. All rights reserved.
CsIX/TRU Grout Feasibility Study
DOE Office of Scientific and Technical Information (OSTI.GOV)
S. J. Losinski; C. M. Barnes; B. K. Grover
A settlement agreement between the Department of Energy (DOE) and the State of Idaho mandates that liquid waste now stored at the Idaho Nuclear Technology Engineering Center (INTEC - formerly the Idaho Chemical Processing Plant, ICPP) will be calcined by the end of year 2012. This study investigates an alternative treatment of the liquid waste that removes undissolved solids (UDS) by filtration and removes cesium by ion exchange followed by cement-based grouting of the remaining liquid into 55-gal drums. Operations are assumed to be from January 2008 through December 2012. The grouted waste will be contact-handled and will be shippedmore » to the Waste Isolation Pilot Plant (WIPP) in New Mexico for disposal. The small volume of secondary wastes such as the filtered solids and cesium sorbent (resin) would remain in storage at the Idaho National Engineering and Environmental Laboratory for treatment and disposal under another project, with an option to dispose of the filtered solids as a r emote-handled waste at WIPP.« less
NASA Astrophysics Data System (ADS)
Makó, Éva; Kovács, András; Ható, Zoltán; Kristóf, Tamás
2015-12-01
Recent experimental and simulation findings with kaolinite-methanol intercalation complexes raised the question of the existence of more stable structures in wet and dry state, which has not been fully cleared up yet. Experimental and molecular simulation analyses were used to investigate different types of kaolinite-methanol complexes, revealing their real structures. Cost-efficient homogenization methods were applied to synthesize the kaolinite-dimethyl sulfoxide and kaolinite-urea pre-intercalation complexes of the kaolinite-methanol ones. The tested homogenization method required an order of magnitude lower amount of reagents than the generally applied solution method. The influence of the type of pre-intercalated molecules and of the wetting or drying (at room temperature and at 150 °C) procedure on the intercalation was characterized experimentally by X-ray diffraction and thermal analysis. Consistent with the suggestion from the present simulations, 1.12-nm and 0.83-nm stable kaolinite-methanol complexes were identified. For these complexes, our molecular simulations predict either single-layered structures of mobile methanol/water molecules or non-intercalated structures of methoxy-functionalized kaolinite. We found that the methoxy-modified kaolinite can easily be intercalated by liquid methanol.
Residence time effects on technetium reduction in slag-based cementitious materials.
Arai, Yuji; Powell, Brian A; Kaplan, D I
2018-01-15
A long-term disposal of technetium-99 ( 99 Tc) has been considered in a type of cementitious formulation, slag-based grout, at the U.S. Department of Energy, Savannah River Site, Aiken SC, U.S.A. Blast furnace slag, which contains S and Fe electron donors, has been used in a mixture with fly ash, and Portland cement to immobilize 99 Tc(VII)O 4 - (aq) in low level radioactive waste via reductive precipitation reaction. However the long-term stability of Tc(IV) species is not clearly understood as oxygen gradually diffuses into the solid structure. In this study, aging effects of Tc speciation were investigated as a function of depth (<2.5cm) in slag-based grout using X-ray absorption spectroscopy. All of Fe(II) in solids was oxidized to Fe(III) after 117d. However, elemental S, sulfide, and sulfoxide persists at the 0-8mm depths even after 485d, suggesting the presence of a reduced zone below the surface few millimeters. Pertechnetate was successfully reduced to Tc(IV) after 29d. Distorted hydrolyzed Tc(IV) octahedral molecules were partially sulfidized and or polymerized at all depths (0-8mm) and were stable in 485d aged sample. The results of this study suggest that variable S species contribute to stabilize the partially sulfidized Tc(IV) species in aged slag-based grout. Copyright © 2017 Elsevier B.V. All rights reserved.
Esteban, María Dolores; Rodríguez, Raúl Rubén; Ibanco, Francisco José; Sánchez, Isidro
2017-01-01
At present, sustainability is of major importance in the cement industry, and the use of additions such as silica fume as clinker replacement contributes towards that goal. Special foundations, and particularly micropiles, are one of the most suitable areas for the use of sustainable cements. The aim of this research is to analyse the effects in the very long-term (for 600 days) produced by sulphate attack in the microstructure of grouts for micropiles in which OPC (ordinary Portland cement) has been replaced by 5% and 10% silica fume. This line of study is building on a previous work, where these effects were studied in slag and fly ash grouts. Grouts made using a commercial sulphate-resisting Portland cement were also studied. The non-destructive impedance spectroscopy technique, mercury intrusion porosimetry, and Wenner resistivity testing were used. Mass variation and the compressive strength have also been analysed. Apparently, impedance spectroscopy is the most suitable technique for studying sulphate attack development. According to the results obtained, grouts for micropiles with a content of silica fume up to 10% and exposed to an aggressive sulphate medium, have a similar or even better behaviour in the very long-term, compared to grouts prepared using sulphate-resisting Portland cement. PMID:28767078
Ortega, José Marcos; Esteban, María Dolores; Rodríguez, Raúl Rubén; Pastor, José Luis; Ibanco, Francisco José; Sánchez, Isidro; Climent, Miguel Ángel
2017-08-02
At present, sustainability is of major importance in the cement industry, and the use of additions such as silica fume as clinker replacement contributes towards that goal. Special foundations, and particularly micropiles, are one of the most suitable areas for the use of sustainable cements. The aim of this research is to analyse the effects in the very long-term (for 600 days) produced by sulphate attack in the microstructure of grouts for micropiles in which OPC (ordinary Portland cement) has been replaced by 5% and 10% silica fume. This line of study is building on a previous work, where these effects were studied in slag and fly ash grouts. Grouts made using a commercial sulphate-resisting Portland cement were also studied. The non-destructive impedance spectroscopy technique, mercury intrusion porosimetry, and Wenner resistivity testing were used. Mass variation and the compressive strength have also been analysed. Apparently, impedance spectroscopy is the most suitable technique for studying sulphate attack development. According to the results obtained, grouts for micropiles with a content of silica fume up to 10% and exposed to an aggressive sulphate medium, have a similar or even better behaviour in the very long-term, compared to grouts prepared using sulphate-resisting Portland cement.
NASA Astrophysics Data System (ADS)
Xie, Chengyu; Jia, Nan; Shi, Dongping; Lu, Hao
2017-10-01
In order to study the slurry diffusion law during grouting, Richards unsaturated-saturated model was introduced, the definition of the grouting model is clear, the Richards model control equation was established, And the BP neural network was introduced, the improved fluid-solid coupling model was constructed, Through the use of saturated - unsaturated seepage flow model, As well as the overflow boundary iterative solution of the mixed boundary conditions, the free surface is calculated. Engineering practice for an example, with the aid of multi - field coupling analysis software, the diffusion law of slurry was simulated numerically. The results show that the slurry diffusion rule is affected by grouting material, initial pressure and other factors. When the slurry starts, it flows in the cracks along the upper side of the grouting hole, when the pressure gradient is reduced to the critical pressure, that is, to the lower side of the flow, when the slurry diffusion stability, and ultimately its shape like an 8. The slurry is spread evenly from the overall point of view, from the grouting mouth toward the surrounding evenly spread, it gradually reaches saturation by non-saturation, and it is not a purely saturated flow, when the slurry spread and reach a saturated state, the diffusion time is the engineering grouting time.
NASA Astrophysics Data System (ADS)
Egger, Hans; Homayoun, Mandana; Schnabel, Wolfgang
2002-10-01
The Paleocene to lowermost Eocene formations of the Rhenodanubian Flysch were deposited in an abyssal environment at the continental rise to the south of the European Plate. The pattern of paleocurrents indicates a number of small distributary systems for the turbiditic material that entered the basin from the north and was deflected to the east and to the west. Heavy mineral assemblages in the turbidites suggest the erosion of medium-grade metasediments in the Danian and the progressive erosion of underlying metamorphic magmatic rocks in the Thanetian and Ypresian. The most obvious sedimentary event is the breakdown in turbidite sedimentation during the late Danian to the early Thanetian. Remarkably, this starvation of turbidites is associated with high values of chlorite in the clay mineral assemblages of interturbidite shales, indicating increased mechanical erosion of the adjoining land areas. Tectonic uplift of these areas and associated block faulting and tilting is assumed to be responsible for this increase in erosion as well as for the synchronous cutting off of the basin from the source area of the turbidites. This tectonic activity is related to the onset of the collision of the European and the Adriatic Plates. A second major event documented in the Paleogene record is the change from a predominantly siliciclastic system to a carbonate system in the latest Thanetian. Associated with the global negative carbon isotope excursion (CIE) in the upper part of calcareous nannozone NP9, calcareous mudturbidites become the prevailing rock type. Eutrophication of surface waters is indicated by acmes of diatoms, radiolaria and dinoflagellates at the level of the CIE. Together with slightly increased values of kaolinite in the clay mineral assemblages of interturbidite shales, this can be interpreted as a result of increased continental run-off due to high precipitation rates in a humid climate. The top of the increased kaolinite input is poorly constrained because of a very high input of smectite due to volcanic activity in sub-zone NP10a. This igneous activity is assigned to the opening of the Northern Atlantic Ocean and has no geodynamic relevance for the Rhenodanubian Basin.