Palynostratigraphy and depositional environment of Vastan Lignite Mine (Early Eocene), Gujarat, western India

NASA Astrophysics Data System (ADS)

Rao, M. R.; Sahni, Ashok; Rana, R. S.; Verma, Poonam

2013-04-01

Early Eocene sedimentary successions of south Asia, are marked by the development of extensive fossil-bearing, lignite-rich sediments prior to the collision of India with Asia and provide data on contemporary equatorial faunal and vegetational assemblages. One such productive locality in western India is the Vastan Lignite Mine representing approximately a 54-52 Ma sequence dated by the presence of benthic zone marker species, Nummulites burdigalensis burdigalensis. The present study on Vastan Lignite Mine succession is based on the spore-pollen and dinoflagellate cyst assemblages and documents contemporary vegetational changes. 86 genera and 105 species belonging to algal remains (including dinoflagellate cysts), fungal remains, pteridophytic spores and angiospermous pollen grains have been recorded. On the basis of first appearance, acme and decline of palynotaxa, three cenozones have been recognized and broadly reflect changing palaeodepositional environments. These are in ascending stratigraphic order (i) Proxapertites Spp. Cenozone, (ii) Operculodinium centrocarpum Cenozone and (iii) Spinizonocolpites Spp. Cenozone. The basal sequence is lagoonal, palm-dominated and overlain by more open marine conditions with dinoflagellate cysts and at the top, mangrove elements are dominant. The succession has also provided a unique record of fish, lizards, snakes, and mammals.

Characterization of uranium bearing material using x-ray fluorescence and direct gamma-rays measurement techniques

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

Mujaini, M., E-mail: madihah@uniten.edu.my; Chankow, N.; Yusoff, M. Z.

2016-01-22

Uranium ore can be easily detected due to various gamma-ray energies emitted from uranium daughters particularly from {sup 238}U daughters such as {sup 214}Bi, {sup 214}Pb and {sup 226}Ra. After uranium is extracted from uranium ore, only low energy gamma-rays emitted from {sup 235}U may be detected if the detector is placed in close contact to the specimen. In this research, identification and characterization of uranium bearing materials is experimentally investigated using direct measurement of gamma-rays from {sup 235}U in combination with the x-ray fluorescence (XRF) technique. Measurement of gamma-rays can be conducted by using high purity germanium (HPGe) detectormore » or cadmium telluride (CdTe) detector while a {sup 57}Coradioisotope-excited XRF spectrometer using CdTe detector is used for elemental analysis. The proposed technique was tested with various uranium bearing specimens containing natural, depleted and enriched uranium in both metallic and powder forms.« less

In situ mobility of uranium in the presence of nitrate following sulfate-reducing conditions.

PubMed

Paradis, Charles J; Jagadamma, Sindhu; Watson, David B; McKay, Larry D; Hazen, Terry C; Park, Melora; Istok, Jonathan D

2016-04-01

Reoxidation and mobilization of previously reduced and immobilized uranium by dissolved-phase oxidants poses a significant challenge for remediating uranium-contaminated groundwater. Preferential oxidation of reduced sulfur-bearing species, as opposed to reduced uranium-bearing species, has been demonstrated to limit the mobility of uranium at the laboratory scale yet field-scale investigations are lacking. In this study, the mobility of uranium in the presence of nitrate oxidant was investigated in a shallow groundwater system after establishing conditions conducive to uranium reduction and the formation of reduced sulfur-bearing species. A series of three injections of groundwater (200 L) containing U(VI) (5 μM) and amended with ethanol (40 mM) and sulfate (20 mM) were conducted in ten test wells in order to stimulate microbial-mediated reduction of uranium and the formation of reduced sulfur-bearing species. Simultaneous push-pull tests were then conducted in triplicate well clusters to investigate the mobility of U(VI) under three conditions: 1) high nitrate (120 mM), 2) high nitrate (120 mM) with ethanol (30 mM), and 3) low nitrate (2 mM) with ethanol (30 mM). Dilution-adjusted breakthrough curves of ethanol, nitrate, nitrite, sulfate, and U(VI) suggested that nitrate reduction was predominantly coupled to the oxidation of reduced-sulfur bearing species, as opposed to the reoxidation of U(IV), under all three conditions for the duration of the 36-day tests. The amount of sulfate, but not U(VI), recovered during the push-pull tests was substantially more than injected, relative to bromide tracer, under all three conditions and further suggested that reduced sulfur-bearing species were preferentially oxidized under nitrate-reducing conditions. However, some reoxidation of U(IV) was observed under nitrate-reducing conditions and in the absence of detectable nitrate and/or nitrite. This suggested that reduced sulfur-bearing species may not be fully effective at limiting the mobility of uranium in the presence of dissolved and/or solid-phase oxidants. The results of this field study confirmed those of previous laboratory studies which suggested that reoxidation of uranium under nitrate-reducing conditions can be substantially limited by preferential oxidation of reduced sulfur-bearing species. Copyright © 2016 The Authors. Published by Elsevier B.V. All rights reserved.

In situ mobility of uranium in the presence of nitrate following sulfate-reducing conditions

DOE PAGES

Paradis, Charles J.; Jagadamma, Sindhu; Watson, David B.; ...

2016-02-11

Reoxidation and mobilization of previously reduced and immobilized uranium by dissolved phase oxidants poses a significant challenge for remediating uranium-contaminated groundwater. Preferential oxidation of reduced sulfur-bearing species, as opposed to reduced uranium bearing species, has been demonstrated to limit the mobility of uranium at the laboratory scale yet field-scale investigations are lacking. Here in this study, the mobility of uranium in the presence of nitrate oxidant was investigated in a shallow groundwater system after establishing conditions conducive to uranium reduction and the formation of reduced sulfur-bearing species. A series of three injections of groundwater (200 L) containing U(VI) (5 μM)more » and amended with ethanol (40 mM) and sulfate (20 mM) were conducted in ten test wells in order to stimulate microbial mediated reduction of uranium and the formation of reduced sulfur-bearing species. Simultaneous push-pull tests were then conducted in triplicate well clusters to investigate the mobility of U(VI) under three conditions: 1) high nitrate (120 mM), 2) high nitrate (120 mM) with ethanol (30 mM), and 3) low nitrate (2 mM) with ethanol (30 mM). Dilution-adjusted breakthrough curves of ethanol, nitrate, nitrite, sulfate, and U(VI) suggested that nitrate reduction was predominantly coupled to the oxidation of reduced-sulfur bearing species, as opposed to the reoxidation of U(IV), under all three conditions for the duration of the 36-day tests. The amount of sulfate, but not U(VI), recovered during the push-pull tests was substantially more than injected, relative to bromide tracer, under all three conditions and further suggested that reduced sulfur-bearing species were preferentially oxidized under nitrate-reducing conditions. However, some reoxidation of U(IV) was observed under nitrate-reducing conditions and in the absence of detectable nitrate and/or nitrite. This suggested that reduced sulfur-bearing species may not be fully effective at limiting the mobility of uranium in the presence of dissolved and/or solid-phase oxidants. Lastly, the results of this field study confirmed those of previous laboratory studies which suggested that reoxidation of uranium under nitrate-reducing conditions can be substantially limited by preferential oxidation of reduced sulfur-bearing species.« less

National Uranium Resource Evaluation. Volume 1. Summary of the geology and uranium potential of Precambrian conglomerates in southeastern Wyoming

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

Karlstrom, K.E.; Houston, R.S.; Flurkey, A.J.

1981-02-01

A series of uranium-, thorium-, and gold-bearing conglomerates in Late Archean and Early Proterozoic metasedimentary rocks have been discovered in southern Wyoming. The mineral deposits were found by applying the time and strata bound model for the origin of uranium-bearing quartz-pebble conglomerates to favorable rock types within a geologic terrane known from prior regional mapping. No mineral deposits have been discovered that are of current (1981) economic interest, but preliminary resource estimates indicate that over 3418 tons of uranium and over 1996 tons of thorium are present in the Medicine Bow Mountains and that over 440 tons of uranium andmore » 6350 tons of thorium are present in Sierra Madre. Sampling has been inadequate to determine gold resources. High grade uranium deposits have not been detected by work to date but local beds of uranium-bearing conglomerate contain as much as 1380 ppM uranium over a thickness of 0.65 meters. This project has involved geologic mapping at scales from 1/6000 to 1/50,000 detailed sampling, and the evaluation of 48 diamond drill holes, but the area is too large to fully establish the economic potential with the present information. This first volume summarizes the geologic setting and geologic and geochemical characteristics of the uranium-bearing conglomerates. Volume 2 contains supporting geochemical data, lithologic logs from 48 drill holes in Precambrian rocks, and drill site geologic maps and cross-sections from most of the holes. Volume 3 is a geostatistical resource estimate of uranium and thorium in quartz-pebble conglomerates.« less

Uranium- and thorium-bearing pegmatites of the United States

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

Adams, J.W.; Arengi, J.T.; Parrish, I.S.

1980-04-01

This report is part of the National Uranium Resource Evaluation (NURE) Program designed to identify criteria favorable for the occurrence of the world's significant uranium deposits. This project deals specifically with uranium- and thorium-bearing pegmatites in the United States and, in particular, their distribution and origin. From an extensive literature survey and field examination of 44 pegmatite localities in the United States and Canada, the authors have compiled an index to about 300 uranium- and thorium-bearing pegmatites in the United States, maps giving location of these deposits, and an annotated bibliography to some of the most pertinent literature on themore » geology of pegmatites. Pegmatites form from late-state magma differentiates rich in volatile constituents with an attendant aqueous vapor phase. It is the presence of an aqueous phase which results in the development of the variable grain size which characterizes pegmatites. All pegmatites occur in areas of tectonic mobility involving crustal material usually along plate margins. Those pegmatites containing radioactive mineral species show, essentially, a similar distribution to those without radioactive minerals. Criteria such as tectonic setting, magma composition, host rock, and elemental indicators among others, all serve to help delineate areas more favorable for uranium- and thorium-bearing pegmatites. The most useful guide remains the radioactivity exhibited by uranium- and thorium-bearing pegmatites. Although pegmatites are frequently noted as favorable hosts for radioactive minerals, the general paucity and sporadic distribution of these minerals and inherent mining and milling difficulties negate the resource potential of pegmatites for uranium and thorium.« less

Thermodynamic properties of selected uranium compounds and aqueous species at 298.15 K and 1 bar and at higher temperatures; preliminary models for the origin of coffinite deposits

USGS Publications Warehouse

Hemingway, B.S.

1982-01-01

Thermodynamic values for 110 uranium-bearing phases and 28 aqueous uranium solution species (298.15 K and l bar) are tabulated based upon evaluated experimental data (largely from calorimetric experiments) and estimated values. Molar volume data are given for most of the solid phases. Thermodynamic values for 16 uranium-bearing phases are presented for higher temperatures in the form of and as a supplement to U.S. Geological Survey Bulletin 1452 (Robie et al., 1979). The internal consistency of the thermodynamic values reported herein is dependent upon the reliability of the experimental results for several uranium phases that have been used as secondary calorimetric reference phases. The data for the reference phases and for those phases evaluated with respect to the secondary reference phases are discussed. A preliminary model for coffinite formation has been proposed together with an estimate of the free energy of formation of coffinite. Free energy values are estimated for several other uranium-bearing silicate phases that have been reported as secondary uranium phases associated with uranium ore deposits and that could be expected to develop wherever uranium is leached by groundwaters.

Discussions about safety criteria and guidelines for radioactive waste management.

PubMed

Yamamoto, Masafumi

2011-07-01

In Japan, the clearance levels for uranium-bearing waste have been established by the Nuclear Safety Commission (NSC). The criteria for uranium-bearing waste disposal are also necessary; however, the NSC has not concluded the discussion on this subject. Meanwhile, the General Administrative Group of the Radiation Council has concluded the revision of its former recommendation 'Regulatory exemption dose for radioactive solid waste disposal', the dose criteria after the institutional control period for a repository. The Standardization Committee on Radiation Protection in the Japan Health Physics Society (The Committee) also has developed the relevant safety criteria and guidelines for existing exposure situations, which are potentially applicable to uranium-bearing waste disposal. A new working group established by The Committee was initially aimed at developing criteria and guidelines specifically for uranium-bearing waste disposal; however, the aim has been shifted to broader criteria applicable to any radioactive wastes.

Reconnaissance for uranium-bearing carbonaceous rocks in California and adjacent parts of Oregon and Nevada

USGS Publications Warehouse

Moore, George Winfred; Stephens, James G.

1954-01-01

During the summer of 1952 a reconnaissance was conducted in California and parts of Oregon and Nevada in search of new deposits of uranium-bearing carbonaceous rocks. The principal localities found in California where uranium occurs in coal are listed here with. the uranium content of the coal: Newhall prospect, Los Angeles County, 0.020 percent; Fireflex mine, San Benito County, 0.005 percent; American licyaite mine, Amador County, 0.004 percent; and Tesla prospect, Alameda County, 0.003 percent. An oil-saturated sandstone near Edna, San Luis Obispo County, contains 0.002 percent uranium.

Natural radioactivity in stream sediments of Oltet River, Romania

NASA Astrophysics Data System (ADS)

Ion, Adriana

2017-04-01

The concentration of naturally occurring radionuclides (U-238, Th-232 and K-40) in stream sediments of the Oltet River was measured in order to establish the primary sources of radionuclides, the transport pathways and the geochemical factors favouring their mobilisation and concentration in the existing geological context. The Oltet River has a length of 185 Km and crosses the southern central part of the country, being the right tributary of the Olt River. The range in elevation of the watercourse varies between 1963 m in the springs area (Parîng Mountains) and 200 m at the confluence with the Olt River, whereas the relief of the Oltet Basin has a varied character, manifested by the presence of diverse forms of relief, starting with major mountainous heights and ending with low-lying plains regions. In cross section from North to South, the Olteț River cuts metamorphic rocks (schist, gneisses, quartzite, marble, mica-schist's), magmatic rocks (granite and granitoid massifs - intruded by veins of microgranite, aplite, pegmatite and lamprophyre) and limestone, followed by deposits composed of clays, marls, sands and gravels, that are characterized by the presence of lignite seams. 44 stream sediment samples were collected in summer of 2016 from sampling points distributed along the river with an equidistance of about 4 - 5 km. The activity concentrations of the U-238, Th-232 and K-40 were measured by gamma ray spectrometry using HPGe detector (ORTEC) with 26% relative efficiency in multilayer shielding. The reference materials used were IAEA - RGK-1 and IAEA - 314. Analysis was performed on the <2 mm fraction of sediment sample, each sample was counted for 24,000 s. U-238 specific activity in the stream sediments varies between 6.18 and 68.76 Bq/Kg and Th-232 specific activity from 8.12 to 89.28 Bq/Kg, whereas the K-40 specific activity in sediments ranges from 99.01 to 312.16 Bq/Kg. In the upper sector of the Oltet River, concentrations of U-238, Th-232 and K-40 show a good correlation between them and reflect the lithological features, the mechanical degradation of the rocks overcomes their chemical decomposition. In the middle part of the river as result of almost abrupt passage between mountain and hilly terrains increases and concentration of radionuclides; effect of large quantities of clastic material deposited by torrents. The mechanical migration of resistant uranium, thorium and potassium bearing mineral determines the movement of rock particles under moving water effect, and redistribution in alluvial sediments with preservation of the native features. In this zone under the action of biochemical processes and other chemical weathering agents, uranium is released from rocks and penetrates in the superficial circulation area or groundwater. Through this geochemical process the amounts of thorium and potassium released are modest, leaching of uranium being the dominant feature (uranyl ion). The downstream lignite seams are the secondary geochemical barriers in accumulation of uranium; the radiometric data obtained for stream sediments emphasize this enrichment.

Stripping-coal deposits on lower Lignite Creek, Nenana coal field, Alaska

USGS Publications Warehouse

Wahrhaftig, Clyde; Birman, Joseph H.

1954-01-01

Stripping-coal reserves in an area of about 9.4 square miles extending from the Nenana River about 6 miles up the valley of Lignite Creek are estimated to amount to about 95, 000, 000 tons. The stripping-coal reserves are located in the lower and middle members of the Tertiary coal-bearing formation. Five continuous beds in the middle member range in thickness from 5 to 30 feet, and a discontinuous bed at the base of the lower member is about 60 feet thick. Analyses of outcrop samples, as received at the laboratory, show a heating content of 7,500--8,200 Btu, an ash content of 6 to 14 percent, and a moisture content of 25 percent. The reserve estimate is based on a maximum thickness of overburden of 200 feet. Coal below the level of Lignite Creek or its major tributaries was not considered as it was assumed that stripping would be by hydraulic methods. Uncertainties regarding the position of the coal outcrops and the extent of burning of the coal beds are the basis for a recommendation that, where possible, the stripping reserves be tested by drilling. Overburden consists largely of weakly consolidated sandstone and includes some coarse gravel and a few boulders 20 feet or more in diameter. Water for hydraulic mining can be obtained from the Nenana River. Lignite Creek does not appear to be a dependable source. Disposal of debris may affect the channel of the Nenana River causing damage to railroads and structures. Landslides are common in the valley of Lignite Creek and will affect mining operations and transportation routes.

Search for uranium in western United States

USGS Publications Warehouse

McKelvey, Vincent Ellis

1953-01-01

The search for uranium in the United States is one of the most intensive ever made for any metal during our history. The number of prospectors and miners involved is difficult to estimate but some measure of the size of the effort is indicated by the fact that about 500 geologists are employed by government and industry in the work--more than the total number of geologists engaged in the study of all other minerals together except oil. The largest part of the effort has been concentrated in the western states. No single deposit of major importance by world standards has been discovered but the search has led to the discovery of important minable deposits of carnotite and related minerals on the Colorado Plateau; of large, low grade deposits of uranium in phosphates in the northwestern states and in lignites in the Dakotas, Wyoming, Idaho and New Mexico; and of many new and some promising occurrences of uranium in carnotite-like deposits and in vein deposits. Despite the fact that a large number of the districts considered favorable for the occurrence of uranium have already been examined, the outlook for future discoveries is bright, particularly for uranium in vein and in carnotite-like deposits in the Rocky Mountain States.

Uranium association with iron-bearing phases in mill tailings from Gunnar, Canada.

PubMed

Othmane, Guillaume; Allard, Thierry; Morin, Guillaume; Sélo, Madeleine; Brest, Jessica; Llorens, Isabelle; Chen, Ning; Bargar, John R; Fayek, Mostafa; Calas, Georges

2013-11-19

The speciation of uranium was studied in the mill tailings of the Gunnar uranium mine (Saskatchewan, Canada), which operated in the 1950s and 1960s. The nature, quantification, and spatial distribution of uranium-bearing phases were investigated by chemical and mineralogical analyses, fission track mapping, electron microscopy, and X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectroscopies at the U LIII-edge and Fe K-edge. In addition to uranium-containing phases from the ore, uranium is mostly associated with iron-bearing minerals in all tailing sites. XANES and EXAFS data and transmission electron microscopy analyses of the samples with the highest uranium concentrations (∼400-700 mg kg(-1) of U) demonstrate that uranium primarily occurs as monomeric uranyl ions (UO2(2+)), forming inner-sphere surface complexes bound to ferrihydrite (50-70% of the total U) and to a lesser extent to chlorite (30-40% of the total U). Thus, the stability and mobility of uranium at the Gunnar site are mainly influenced by sorption/desorption processes. In this context, acidic pH or alkaline pH with the presence of UO2(2+)- and/or Fe(3+)-complexing agents (e.g., carbonate) could potentially solubilize U in the tailings pore waters.

Host rocks and their alterations as related to uranium-bearing veins in the United States

USGS Publications Warehouse

Walker, George W.

1956-01-01

This paper, dealing with the different kinds of host rocks and their alterations associated with uranium-bearing veins in the United States, is a chapter of a comprehensive report entitled , "Geology of uranium-bearing vein deposits in the United States," in preparation by George W. Walker, Frank W. Osterwald, and others. The comprehensive report will include detailed information on tectonic and structural setting, kinds of host rocks, wall-rock alteration, mineralogy, physical characteristics, processes of deposition, and concepts of origin of uraniferous veins; but, because it will not be completed until sometime in the future, some chapters of the report are being transmitted as they are finished. Part of an introductory chapter to the comprehensive report entitled, "Classification and distribution of uranium-bearing veins in the United States" (Walker and Osterwald, 1956) has already been transmitted; several of the terms used herein are defined in the introductory chapter. Data included in this chapter demonstrate that uranium-bearing veins are: 1) in rocks of nearly all textural, chemical, and mineralogic types; 2) most abundant in holocrystalline, commonly equigranular, igeneous and metamorphic rocks characterized by a moderate to high silica content and and by similar physical properties. Although some of the physiochemical properties of the host rocks are discussed in terms of favorability or nonfavoribility for uranium deposition, the principal purpose of this chapter is to establish the petroloic environment in which uranium-bearing veins have been found. Because favorability or nonfavorability of host rocks is related complexly to the chemistry of ore solutions and to methods or uranium transport and deposition, several hypothetical processes of transport and deposition have been referred to briefly; these and other hypotheses will be outlines and discussed in greater detail in a subsequent chapter. The compilation of data leading to this report and its preparation by a member of the Uranium Research and Resource Section, U.S. Geological Survey, was done on behalf of the Division of Raw Materials, U.S. Atomic Energy Commission. The report is based on both published and unpublished information collected principally by personnel of the U.S. Geological Survey, the U.S. Atomic Energy Commission or its predecessor organization, the Manhattan Engineer District, and to a lesser extent by staff members of other Federal or State agencies and by geologists in private industry. Information concerning foreign uranium-bearing vein deposits has been extracted almost exclusively from published reports; references to these and other data are included at appropriate places.

Method of fabricating a uranium-bearing foil

DOEpatents

Gooch, Jackie G [Seymour, TN; DeMint, Amy L [Kingston, TN

2012-04-24

Methods of fabricating a uranium-bearing foil are described. The foil may be substantially pure uranium, or may be a uranium alloy such as a uranium-molybdenum alloy. The method typically includes a series of hot rolling operations on a cast plate material to form a thin sheet. These hot rolling operations are typically performed using a process where each pass reduces the thickness of the plate by a substantially constant percentage. The sheet is typically then annealed and then cooled. The process typically concludes with a series of cold rolling passes where each pass reduces the thickness of the plate by a substantially constant thickness amount to form the foil.

RECOVERY OF URANIUM VALUES FROM URANIUM BEARING RAW MATERIALS

DOEpatents

Michal, E.J.; Porter, R.R.

1959-06-16

Uranium leaching from ground uranium-bearing raw materials using MnO/sub 2/ in H/sub 2/SO/sub 4/ is described. The MnO/sub 2/ oxidizes U to the leachable hexavalent state. The MnO/sub 2/ does not replace Fe normally added, because the Fe complexes P and catalyzes the MnO/sub 2/ reaction. Three examples of continuous processes are given, but batch operation is also possible. The use of MnO/sub 2/ makes possible recovery of very low U values. (T.R.H.)

Controls on Methane Occurrences in Shallow Aquifers Overlying the Haynesville Shale Gas Field, East Texas.

PubMed

Nicot, Jean-Philippe; Larson, Toti; Darvari, Roxana; Mickler, Patrick; Slotten, Michael; Aldridge, Jordan; Uhlman, Kristine; Costley, Ruth

2017-07-01

Understanding the source of dissolved methane in drinking-water aquifers is critical for assessing potential contributions from hydraulic fracturing in shale plays. Shallow groundwater in the Texas portion of the Haynesville Shale area (13,000 km 2 ) was sampled (70 samples) for methane and other dissolved light alkanes. Most samples were derived from the fresh water bearing Wilcox formations and show little methane except in a localized cluster of 12 water wells (17% of total) in a approximately 30 × 30 km 2 area in Southern Panola County with dissolved methane concentrations less than 10 mg/L. This zone of elevated methane is spatially associated with the termination of an active fault system affecting the entire sedimentary section, including the Haynesville Shale at a depth more than 3.5 km, and with shallow lignite seams of Lower Wilcox age at a depth of 100 to 230 m. The lignite spatial extension overlaps with the cluster. Gas wetness and methane isotope compositions suggest a mixed microbial and thermogenic origin with contribution from lignite beds and from deep thermogenic reservoirs that produce condensate in most of the cluster area. The pathway for methane from the lignite and deeper reservoirs is then provided by the fault system. © 2017, National Ground Water Association.

Seasonal variations of natural radionuclides, minor and trace elements in lake sediments and water in a lignite mining area of North-Western Greece.

PubMed

Noli, Fotini; Tsamos, Panagiotis

2018-05-01

The radiological and chemical pollution of a cluster of four lakes in a lignite mining area of North-Western Greece was investigated using a variety of analytical techniques. Alpha spectrometry was applied to measure the activity concentrations of the uranium radioisotopes (U-234, U-235, and U-238) in waters. The mass activities of U-238, Th-232, and K-40 in sediments were measured by high-resolution gamma spectrometry. Furthermore, the determination of the minor and trace elements was carried out by instrumental neutron activation analysis (INAA) in both water and sediments samples, respectively. Pollution levels were also evaluated by calculating enrichment factors (EFs), contamination factors (CFs) and pollution load index (PLI). The data were discussed taking into account several parameters such as the distance from the pollution source, temperature, and location and showed that the environmental impact in this region could not be considered as negligible. The deviation of the isotopic ratio of U-234/U-238 from the equilibrium value indicated waters with intensive dissolution of uranium. The activity values in both waters and sediments found to be low in cool periods and increased in warm periods. Moreover, the concentrations of the elements U, Zn, and Fe were raised in water samples indicating possible pollution as well as the CFs and PLI denoted accumulation in the sediments and moderate to severe contamination for Zn and Cr in some cases.

Integrated stratigraphy of Paleocene lignite seams of the fluvial Tullock Formation, Montana (USA).

NASA Astrophysics Data System (ADS)

Noorbergen, Lars J.; Kuiper, Klaudia F.; Hilgen, Frederik J.; Krijgsman, Wout; Dekkers, Mark J.; Smit, Jan; Abels, Hemmo A.

2015-04-01

Coal-bearing fluvial sedimentation is generally thought to be dominated by autogenic processes that are processes intrinsic to the sedimentary system. Ongoing research however suggests that several fluvial processes such as floodplain inundation and avulsion, can also be controlled by external forcing such as orbital climate change. Still, the exact role of orbital climate forcing in fluvial sediments is difficult to decipher since riverine deposits are complicated by variable sedimentation rates including erosion of previously deposited material, by lateral heterogeneity of sedimentation, and by scarcity of independent dating methods. The early Paleocene lignite-bearing Tullock Formation of the Williston Basin in eastern Montana represents a record of fluvial sedimentation that is perfectly exposed and, displays a seemingly regular alternation of sandstones and lignite seams. These coal beds contain multiple volcanic ash layers. Here, we use an integrated stratigraphic approach (litho- and magnetostratigraphy, geochemical fingerprinting and radio-isotope dating of volcanic ash layers) to establish a high-resolution time frame for the early Paleocene fluvial sediments. First age estimations indicate that the Tullock Formation in Eastern Montana was deposited over a time span of ~ 1000 kyr subsequent to the Cretaceous - Paleogene boundary, dated at ~ 65.95 Ma [1]. Initial high-resolution magnetostratigraphy revealed the occurrence of the C29r/C29n polarity reversal which was stratigraphic consistent at different field locations. We investigate the regional significance of sedimentary change at multiple sites of the same age in order to provide improved insight on the role of orbital forcing in fluvial coal formation. References: [1] Kuiper, K.F., Deino, A., Hilgen, F.J., Krijgsman, W., Renne, P.R., Wijbrans, J.R. (2008). Synchronizing Rock Clocks of Earth History. Science 320, 500-504.

Sedimentology of gas-bearing Devonian shales of the Appalachian Basin

NASA Astrophysics Data System (ADS)

Potter, P. E.; Maynard, J. B.; Pryor, W. A.

1981-01-01

Sedimentology of the Devonian shales and its relationship to gas, oil, and uranium are reported. Information about the gas bearing Devonian shales of the Appalachian Basin is organized in the following sections: paleogeography and basin analysis; lithology and internal stratigraphy; paleontology; mineralogy, petrology, and chemistry; and gas oil, and uranium.

PREPARATION OF REFRACTORY OXIDE CRYSTALS

DOEpatents

Grimes, W.R.; Shaffer, J.H.; Watson, G.M.

1962-11-13

A method is given for preparing uranium dioxide, thorium oxide, and beryllium oxide in the form of enlarged individual crystals. The surface of a fused alkali metal halide melt containing dissolved uranium, thorium, or beryllium values is contacted with a water-vapor-bearing inert gas stream at a rate of 5 to 10 cubic centimeters per minute per square centimeter of melt surface area. Growth of individual crystals is obtained by prolonged contact. Beryllium oxide-coated uranium dioxide crystals are prepared by disposing uranium dioxide crystals 5 to 20 microns in diameter in a beryllium-containing melt and contacting the melt with a water-vapor-bearing inert gas stream in the same manner. (AEC)

Estimation and mapping of uranium content of geological units in France.

PubMed

Ielsch, G; Cuney, M; Buscail, F; Rossi, F; Leon, A; Cushing, M E

2017-01-01

In France, natural radiation accounts for most of the population exposure to ionizing radiation. The Institute for Radiological Protection and Nuclear Safety (IRSN) carries out studies to evaluate the variability of natural radioactivity over the French territory. In this framework, the present study consisted in the evaluation of uranium concentrations in bedrocks. The objective was to provide estimate of uranium content of each geological unit defined in the geological map of France (1:1,000,000). The methodology was based on the interpretation of existing geochemical data (results of whole rock sample analysis) and the knowledge of petrology and lithology of the geological units, which allowed obtaining a first estimate of the uranium content of rocks. Then, this first estimate was improved thanks to some additional information. For example, some particular or regional sedimentary rocks which could present uranium contents higher than those generally observed for these lithologies, were identified. Moreover, databases on mining provided information on the location of uranium and coal/lignite mines and thus indicated the location of particular uranium-rich rocks. The geological units, defined from their boundaries extracted from the geological map of France (1:1,000,000), were finally classified into 5 categories based on their mean uranium content. The map obtained provided useful data for establishing the geogenic radon map of France, but also for mapping countrywide exposure to terrestrial radiation and for the evaluation of background levels of natural radioactivity used for impact assessment of anthropogenic activities. Copyright © 2016 Elsevier Ltd. All rights reserved.

Reconnaissance for uranium in asphalt-bearing rocks in the western states

USGS Publications Warehouse

Hail, William James

1955-01-01

Evaluation of field data indicates that naturally occurring asphalts with a relatively high uranium content probably originated in, or migrated through, rocks that contain more than average amounts of uranium. It is believed that some of the uranium was present as an original constituent of the oil but that some uranium may have been introduced during migration of the oil.

Uranium content and leachable fraction of fluorspars

USGS Publications Warehouse

Landa, E.R.; Councell, T.B.

2000-01-01

Much attention in the radiological health community has recently focused on the management and regulation of naturally occurring radioactive materials. Although uranium-bearing minerals are present in a variety of fluorspar deposits, their potential consideration as naturally occurring radioactive materials has received only limited recognition. The uranium content of 28 samples of acid- and cryolite-grade (>97% CaF2) fluorspar from the National Defense Stockpile was found to range from 120 to 24,200 ??g kg-1, with a mean of 2,145 ??g kg-1. As a point of comparison, the average concentration of uranium in the upper crust of the earth is about 2,500 ??g kg-1. Leachability of this uranium was assessed by means of the Toxicity Characteristic Leaching Procedure (TCLP). The TCLP extractable fraction ranged from 1 to 98%, with a mean of 24% of the total uranium. The typically low concentrations of uranium seen in these materials probably reflects the removal of uranium-bearing mineral phases during the beneficiation of the crude fluorspar ore to achieve industrial specifications. Future NORM studies should examine crude fluorspar ores and flotation tailings.

DEEP BIOSPHERE. Exploring deep microbial life in coal-bearing sediment down to ~2.5 km below the ocean floor.

PubMed

Inagaki, F; Hinrichs, K-U; Kubo, Y; Bowles, M W; Heuer, V B; Hong, W-L; Hoshino, T; Ijiri, A; Imachi, H; Ito, M; Kaneko, M; Lever, M A; Lin, Y-S; Methé, B A; Morita, S; Morono, Y; Tanikawa, W; Bihan, M; Bowden, S A; Elvert, M; Glombitza, C; Gross, D; Harrington, G J; Hori, T; Li, K; Limmer, D; Liu, C-H; Murayama, M; Ohkouchi, N; Ono, S; Park, Y-S; Phillips, S C; Prieto-Mollar, X; Purkey, M; Riedinger, N; Sanada, Y; Sauvage, J; Snyder, G; Susilawati, R; Takano, Y; Tasumi, E; Terada, T; Tomaru, H; Trembath-Reichert, E; Wang, D T; Yamada, Y

2015-07-24

Microbial life inhabits deeply buried marine sediments, but the extent of this vast ecosystem remains poorly constrained. Here we provide evidence for the existence of microbial communities in ~40° to 60°C sediment associated with lignite coal beds at ~1.5 to 2.5 km below the seafloor in the Pacific Ocean off Japan. Microbial methanogenesis was indicated by the isotopic compositions of methane and carbon dioxide, biomarkers, cultivation data, and gas compositions. Concentrations of indigenous microbial cells below 1.5 km ranged from <10 to ~10(4) cells cm(-3). Peak concentrations occurred in lignite layers, where communities differed markedly from shallower subseafloor communities and instead resembled organotrophic communities in forest soils. This suggests that terrigenous sediments retain indigenous community members tens of millions of years after burial in the seabed. Copyright © 2015, American Association for the Advancement of Science.

Precambrian uranium-bearing quartz-pebble conglomerates: exploration model and United States resource potential

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

Houston, R.S.; Karlstrom, K.E.

1979-11-01

Uranium has been discovered in fluvial quartz-pebble conglomerates in most of the Precambrian shield areas of the world, including the Canadian, African, South American, Indian, Baltic, and Australian shields. Occurrences in these and other areas are shown. Two of these occurrences, the Huronian supergroup of Canada and the Witwatersrand deposit of South Africa contain 20 to 30 percent of the planet's known uranium reserves. Thus it is critical that we understand the origin of these deposits and develop exploration models that can aid in finding new deposits. Inasmuch as these uranium-bearing conglomerates are confined almost entirely to rocks of Precambrianmore » age, Part I of this review begins with a discussion of Precambrian geology as it applies to the conglomerates. This is followed by a discussion of genetic concepts, a discussion of unresolved problems, and finally a suggested exploration model. Part II summarizes known and potential occurrences of Precambrian fossil placers in the world and evaluates them in terms of the suggested exploration model. Part III discusses the potential for important Precambrian fossil-placer uranium deposits in the United States and includes suggestions that may be helpful in establishing an exploration program in this country. Part III also brings together new (1975-1978) data on uranium occurrences in the Precambrian of the Wyoming Province. Part IV is a complete bibliography of Precambrian fossil placers, divided according to geographical areas. In total, this paper is designed to be a comprehensive review of Precambrian uranium-bearing fossil placers which will be of use to uranium explorationists and to students of Precambrian geology.« less

Characterization of uranium redox state in organic-rich Eocene sediments.

PubMed

Cumberland, Susan A; Etschmann, Barbara; Brugger, Joël; Douglas, Grant; Evans, Katy; Fisher, Louise; Kappen, Peter; Moreau, John W

2018-03-01

The presence of organic matter (OM) has a profound impact on uranium (U) redox cycling, either limiting or promoting the mobility of U via binding, reduction, or complexation. To understand the interactions between OM and U, we characterised U oxidation state and speciation in nine OM-rich sediment cores (18 samples), plus a lignite sample from the Mulga Rock polymetallic deposit in Western Australia. Uranium was unevenly dispersed within the analysed samples with 84% of the total U occurring in samples containing >21 wt % OM. Analyses of U speciation, including x-ray absorption spectroscopy and bicarbonate extractions, revealed that U existed predominately (∼71%) as U(VI), despite the low pH (4.5) and nominally reducing conditions within the sediments. Furthermore, low extractability by water, but high extractability by a bi-carbonate solution, indicated a strong association of U with particulate OM. The unexpectedly high proportion of U(VI) relative to U(IV) within the OM-rich sediments implies that OM itself does not readily reduce U, and the reduction of U is not a requirement for immobilizing uranium in OM-rich deposits. The fact that OM can play a significant role in limiting the mobility and reduction of U(VI) in sediments is important for both U-mining and remediation. Copyright © 2017 Elsevier Ltd. All rights reserved.

Natural radioactivity in lignite samples from open pit mines "Kolubara", Serbia--risk assessment.

PubMed

Ðurašević, M; Kandić, A; Stefanović, P; Vukanac, I; Sešlak, B; Milošević, Z; Marković, T

2014-05-01

Coal as fossil fuel mainly contains naturally occurring radionuclides from the uranium and thorium series and (40)K. Use of coal, primarily in industry, as a result has dispersion of radioactive material from coal in and through air and water. The aim of this study was to determine the activity concentrations of natural radionuclides in coal samples from open pit mines "Kolubara" and to evaluate its effect on population health. The results showed that all measured and calculated values were below the limits recommended in international legislation. © 2013 Published by Elsevier Ltd.

Rapid Dissolution of Soluble Uranyl Phases in Arid, Mine-Impacted Catchments Near Church Rock, NM

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

deLemos, J.L.; Bostick, B.C.; Quicksall, A.N.

2009-05-14

We tested the hypothesis that runoff of uranium-bearing particles from mining waste disposal areas was a significant mechanism for redistribution of uranium in the northeastern part of the Upper Puerco River watershed (New Mexico). However, our results were not consistent with this hypothesis. Analysis of >100 sediment and suspended sediment samples collected adjacent to and downstream from uranium source areas indicated that uranium levels in the majority of the samples were not elevated above background. Samples collected within 50 m of a known waste disposal site were subjected to detailed geochemical characterization. Uranium in these samples was found to bemore » highly soluble; treatment with synthetic pore water for 24 h caused dissolution of 10-50% of total uranium in the samples. Equilibrium uranium concentrations in pore water were >4.0 mg/L and were sustained in repeated wetting events, effectively depleting soluble uranium from the solid phase. The dissolution rate of uranium appeared to be controlled by solid-phase diffusion of uranium from within uranium-bearing mineral particles. X-ray adsorption spectroscopy indicated the presence of a soluble uranyl silicate, and possibly a uranyl phosphate. These phases were exhausted in transported sediment suggesting that uranium was readily mobilized from sediments in the Upper Puerco watershed and transported in the dissolved load. These results could have significance for uranium risk assessment as well as mining waste management and cleanup efforts.« less

Rapid Dissolution of Soluble Uranyl Phases in Arid, Mine-Impacted Catchments near Church Rock, NM

PubMed Central

DELEMOS, JAMIE L.; BOSTICK, BENJAMIN C.; QUICKSALL, ANDREW N.; LANDIS, JOSHUA D.; GEORGE, CHRISTINE C.; SLAGOWSKI, NAOMI L.; ROCK, TOMMY; BRUGGE, DOUG; LEWIS, JOHNNYE; DURANT, JOHN L.

2008-01-01

We tested the hypothesis that runoff of uranium-bearing particles from mining waste disposal areas was a significant mechanism for redistribution of uranium in the northeastern part of the Upper Puerco River watershed (New Mexico). However, our results were not consistent with this hypothesis. Analysis of >100 sediment and suspended sediment samples collected adjacent to and downstream from uranium source areas indicated that uranium levels in the majority of the samples were not elevated above background. Samples collected within 50 m of a known waste disposal site were subjected to detailed geochemical characterization. Uranium in these samples was found to be highly soluble; treatment with synthetic pore water for 24 h caused dissolution of 10–50% of total uranium in the samples. Equilibrium uranium concentrations in pore water were >4.0 mg/L and were sustained in repeated wetting events, effectively depleting soluble uranium from the solid phase. The dissolution rate of uranium appeared to be controlled by solid-phase diffusion of uranium from within uranium-bearing mineral particles. X-ray adsorption spectroscopy indicated the presence of a soluble uranyl silicate, and possibly a uranyl phosphate. These phases were exhausted in transported sediment suggesting that uranium was readily mobilized from sediments in the Upper Puerco watershed and transported in the dissolved load. These results could have significance for uranium risk assessment as well as mining waste management and cleanup efforts. PMID:18589950

Localized sulfate-reducing zones in a coastal plain aquifer

USGS Publications Warehouse

Brown, C.J.; Coates, J.D.; Schoonen, M.A.A.

1999-01-01

High concentrations of dissolved iron in ground water of coastal plain or alluvial aquifers contribute to the biofouling of public supply wells for which treatment and remediation is costly. Many of these aquifers, however, contain zones in which microbial sulfate reduction and the associated precipitation of iron-sulfide minerals decreases iron mobility. The principal water-bearing aquifer (Magothy Aquifer of Cretaceous age) in Suffolk County, New York, contains localized sulfate-reducing zones in and near lignite deposits, which generally are associated with clay lenses. Microbial analyses of core samples amended with [14C]-acetate indicate that microbial sulfate reduction is the predominant terminal-electron-accepting process (TEAP) in poorly permeable, lignite-rich sediments at shallow depths and near the ground water divide. The sulfate-reducing zones are characterized by abundant lignite and iron-sulfide minerals, low concentrations of Fe(III) oxyhydroxides, and by proximity to clay lenses that contain pore water with relatively high concentrations of sulfate and dissolved organic carbon. The low permeability of these zones and, hence, the long residence time of ground water within them, permit the preservation and (or) allow the formation of iron-sulfide minerals, including pyrite and marcasite. Both sulfate-reducing bacteria (SRB) and iron-reducing bacteria (IRB) are present beneath and beyond the shallow sulfate-reducing zones. A unique Fe(III)-reducing organism, MD-612, was found in core sediments from a depth of 187 m near the southern shore of Long Island. The distribution of poorly permeable, lignite-rich, sulfate-reducing zones with decreased iron concentration is varied within the principal aquifer and accounts for the observed distribution of dissolved sulfate, iron, and iron sulfides in the aquifer. Locating such zones for the placement of production wells would be difficult, however, because these zones are of limited aerial extent.

Contribution of Uranium-Bearing Evaporites to Plume Persistence Issues at a Former Uranium Mill Site Riverton, Wyoming, USA

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

Johnson, Raymond; Dam, William; Campbell, Sam

2016-08-01

• Evaporites occur in an unsaturated silt layer, which is underlain by a sand and gravel aquifer. • These evaporites are rich in chloride across the site. • Uranium concentrations are higher in the evaporites that overlie the uranium contaminant plume. • Flooding can solubilize the evaporites in the silt layer and release chloride, sulfate (not shown), and uranium into the underlyingsand and gravel aquifer. • The uranium-rich evaporites can delay natural flushing, creating plume persistence near the Little Wind River.

METHOD OF OPERATING A CALUTRON

DOEpatents

Davidson, P.H.

1960-01-12

A method of operating an electromagnetic isotope separator of the calutron class is reported whereby uranium tetrachloride is produced at a controlled rate within the source rather than betng introduced therein as was formerly practiced. This is accomplished by placing a uranium-bearing material, such as uranium metal, uranium trichloride, or uranium carbide in the charge receptacle of the calutron, heating this material to about to produce uranium tetrachloride vapor at a rate controlled by the chlorine gas flow into the source. The vapor is subsequently ionized by an electric arc and mass separated by conventional calutron methods.

URANIUM RECOVERY PROCESS

DOEpatents

Bailes, R.H.; Long, R.S.; Olson, R.S.; Kerlinger, H.O.

1959-02-10

A method is described for recovering uranium values from uranium bearing phosphate solutions such as are encountered in the manufacture of phosphate fertilizers. The solution is first treated with a reducing agent to obtain all the uranium in the tetravalent state. Following this reduction, the solution is treated to co-precipitate the rcduced uranium as a fluoride, together with other insoluble fluorides, thereby accomplishing a substantially complete recovery of even trace amounts of uranium from the phosphate solution. This precipitate usually takes the form of a complex fluoride precipitate, and after appropriate pre-treatment, the uranium fluorides are leached from this precipitate and rccovered from the leach solution.

Germanium geochemistry and mineralogy

USGS Publications Warehouse

Bernstein, L.R.

1985-01-01

Germanium is enriched in the following geologic environments: 1. (1) iron meteorites and terrestrial iron-nickel; 2. (2) sulfide ore deposits, particularly those hosted by sedimentary rocks; 3. (3) iron oxide deposits; 4. (4) oxidized zones of Ge-bearing sulfide deposits; 5. (5) pegmatites, greisens, and skarns; and 6. (6) coal and lignitized wood. In silicate melts, Ge is highly siderophile in the presence of native iron-nickel; otherwise, it is highly lithophile. Among silicate minerals, Ge is concentrated in those having less polymerized silicate tetrahedra such as olivine and topaz. In deposits formed from hydrothermal solutions, Ge tends to be enriched mostly in either sulfides or in fluorine-bearing phases; it is thus concentrated both in some hydrothermal sulfide deposits and in pegmatites, greisens, and skarns. In sulfide deposits that formed from solutions having low to moderate sulfur activity, Ge is concentrated in sphalerite in amounts up to 3000 ppm. Sulfide deposits that formed from solutions having higher sulfur activity allowed Ge to either form its own sulfides, particularly with Cu, or to substitute for As, Sn, or other metals in sulfosalts. The Ge in hydrothermal fluids probably derives from enrichment during the fractional crystallization of igneous fluids, or is due to the incorporation of Ge from the country rocks, particularly from those containing organic material. Germanium bonds to lignin-derivative organic compounds that are found in peat and lignite, accounting for its common concentration in coals and related organic material. Germanium is precipitated from water together with iron hydroxide, accounting for its concentration in some sedimentary and supergene iron oxide deposits. It also is able to substitute for Fe in magnetite in a variety of geologic environments. In the oxidized zone of Ge-bearing sulfide deposits, Ge is concentrated in oxides, hydroxides, and hydroxy-sulfates, sometimes forming its own minerals. It is particularly enriched in some iron- and manganese-bearing oxides and hydroxides, including goethite (up to 5300 ppm) and hematite (up to 7000 ppm). ?? 1985.

Uranium-bearing copper deposits in the Coyote district, Mora County, New Mexico

USGS Publications Warehouse

Zeller, H.D.; Baltz, Elmer Harold

1954-01-01

Uranium-bearing copper deposits occur in steeply dipping beds of the Sangre de Cristo formation of Pennsylvanian and Permian(?) age south of Coyote, Mora County, N. Mex. Mapping and sampling of these deposits indicate that they are found in lenticular carbonaceous zones in shales and arkosic sandstones. Samples from these zones contain as much as 0.067 percent uranium and average 3 percent copper. Metatyuyamunite is dissemihatedin some of the arkosic sandstone beds, and uraninite is present in some of the copper sulfide nodules occurring in the shale. These sulfide nodules are composed principally of chalcocite but include some bornite, covellite, pyrite, and malachite. Most of the samples were collected near the surface from the weathered zone. The copper and uranium were probably deposited with the sediments and concentrated into zones during compaction and lithification. Carbonaceous material in the Sangre de Cristo formation provided the environment that precipitated uranium and copper from mineral-charged connate waters forced from the clayey sediments.

SOLVENT EXTRACTION OF URANIUM VALUES

DOEpatents

Feder, H.M.; Ader, M.; Ross, L.E.

1959-02-01

A process is presented for extracting uranium salt from aqueous acidic solutions by organic solvent extraction. It consists in contacting the uranium bearing solution with a water immiscible dialkylacetamide having at least 8 carbon atoms in the molecule. Mentioned as a preferred extractant is dibutylacetamide. The organic solvent is usually used with a diluent such as kerosene or CCl/sub 4/.

Occurrences of uranium-bearing minerals in the St. Kevin District, Lake County, Colorado

USGS Publications Warehouse

Pierson, C.T.; Singewald, Q.D.

1953-01-01

None of the uranium occurrences are of commercial importance. They are for the most part in non-glaciated terrane, which has been subjected to a very long period of weathering.  Thus, chemical leaching within the zone of weathering may have greatly reduced the uranium content of material near the surface, and occurrences of even small quantities of secondary uranium minerals might be related to stronger, primary concentrations at depth.

REMOVAL OF URANIUM FROM ORGANIC LIQUIDS

DOEpatents

Vavalides, S.P.

1959-08-25

A process is described for recovering small quantities of uranium from organic liquids such as hydrocarbon oils. halogen-substituted hydrocarbons, and alcohols. The organic liquid is contacted with a comminuted alkaline earth hydroxide, calcium hydroxide particularly, and the resulting uranium-bearing solid is separated from the liquid by filtration. Uranium may then be recovered from the solid by means of dissolution in nitric acid and conventional extraction with an organic solvent such as tributyl phosphate.

Process for recovering uranium from waste hydrocarbon oils containing the same. [Uranium contaminated lubricating oils from gaseous diffusion compressors

DOEpatents

Conrad, M.C.; Getz, P.A.; Hickman, J.E.; Payne, L.D.

1982-06-29

The invention is a process for the recovery of uranium from uranium-bearing hydrocarbon oils containing carboxylic acid as a degradation product. In one aspect, the invention comprises providing an emulsion of water and the oil, heating the same to a temperature effecting conversion of the emulsion to an organic phase and to an acidic aqueous phase containing uranium carboxylate, and recovering the uranium from the aqueous phase. The process is effective, simple and comparatively inexpensive. It avoids the use of toxic reagents and the formation of undesirable intermediates.

PROCESS OF RECOVERING URANIUM

DOEpatents

Carter, J.M.; Larson, C.E.

1958-10-01

A process is presented for recovering uranium values from calutron deposits. The process consists in treating such deposits to produce an oxidlzed acidic solution containing uranium together with the following imparities: Cu, Fe, Cr, Ni, Mn, Zn. The uranium is recovered from such an impurity-bearing solution by adjusting the pH of the solution to the range 1.5 to 3.0 and then treating the solution with hydrogen peroxide. This results in the precipitation of uranium peroxide which is substantially free of the metal impurities in the solution. The peroxide precipitate is then separated from the solution, washed, and calcined to produce uranium trioxide.

The Robinson and Weatherly uraniferous pyrobitumen deposits near Placerville, San Miguel County, Colorado

USGS Publications Warehouse

Wilmarth, V.R.; Vickers, R.C.

1953-01-01

Uranium deposits that contain uraniferous pyrobitumen of possible hydrothermal origin occur at the Weatherly and Robinson properties near Placerville, San Miguel County, Colo. These deposits were mined for copper, silver, and gold more than 50 years ago and were developed for uranium in 1950. The Robinson property, half a mile east of Placerville, consists of the White Spar, New Discovery Lode, and Barbara Jo claims. The rocks in this area are nearly horizontal sandstones, shales, limestones, and conglomerates of the Cutler formation of Permian age and the Dolores formation of Triassic and Jurassic (?) age. These rocks have been faulted extensively and intruded by a Tertiary (?) andesite porphyry dike. Uranium-bearing pyrobitumen associated with tennantite, tetrahedrite, galena, sphalerite, chalcopyrite, bornite, azurite, malachite, calcite, barite, and quartz occurs in a lenticular body as much as 40 feet long and 6 feet wide along a northwest-trending, steeply dipping normal fault. The uranium content of eleven samples from the uranium deposit ranges from 0.001 to 0.045 percent uranium and averages about 0.02 percent uranium. The Weatherly property, about a mile northwest of Placerville, consists of the Black King claims nos. 1, 4, and 5. The rocks in this area include the complexly faulted Cutler formation of Permian age and the Dolores formation of Triassic and Jurassic (?) age. Uranium-bearing pyrobitumen arid uranophane occur, along a northwest-trending, steeply dipping normal fault and in the sedimentary rocks on the hanging wall of the fault. Lens-shaped deposits in the fault zone are as much as 6 feet long and 2 feet wide and contain as much as 9 percent uranium; whereas channel samples across the fault zone contain from 0.001 to 0.014 percent uranium. Tetrahedrite, chalcopyrite, galena, sphalerite, fuchsite, malachite, azurite, erythrite, bornite, and molybdite in a gangue of pyrite, calcite, barite, and quartz are associated with the uraniferous material. In the sedimentary rocks on the hanging wall, uranium-bearing pyrobitumen occurs in replacement lenses as much as,8 inches wide and 6 feet long, and in nodules as much as 6 inches in diameter for approximately 100 feet away from the fault. Pyrite and calcite are closely associated with the uraniferous material in the sedimentary rocks. Samples from the replacement bodies contain from 0. 007 to 1.4 percent uranium.

Kinetic study of the thermal decomposition of uranium metaphosphate, U(PO3)4, into uranium pyrophosphate, UP2O7

NASA Astrophysics Data System (ADS)

Yang, Hee-Chul; Kim, Hyung-Ju; Lee, Si-Young; Yang, In-Hwan; Chung, Dong-Yong

2017-06-01

The thermochemical properties of uranium compounds have attracted much interest in relation to thermochemical treatments and the safe disposal of radioactive waste bearing uranium compounds. The characteristics of the thermal decomposition of uranium metaphosphate, U(PO3)4, into uranium pyrophosphate, UP2O7, have been studied from the view point of reaction kinetics and acting mechanisms. A mixture of U(PO3)4 and UP2O7 was prepared from the pyrolysis residue of uranium-bearing spent TBP. A kinetic analysis of the reaction of U(PO3)4 into UP2O7 was conducted using an isoconversional method and a master plot method on the basis of data from a non-isothermal thermogravimetric analysis. The thermal decomposition of U(PO3)4 into UP2O7 followed a single-step reaction with an activation energy of 175.29 ± 1.58 kJ mol-1. The most probable kinetic model was determined as a type of nucleation and nuclei-growth models, the Avrami-Erofeev model (A3), which describes that there are certain restrictions on nuclei growth of UP2O7 during the solid-state decomposition of U(PO3)4.

Geochemical hosts of solubilized radionuclides in uranium mill tailings

USGS Publications Warehouse

Landa, E.R.; Bush, C.A.

1990-01-01

The solubilization and subsequent resorption of radionuclides by ore components or by reaction products during the milling of uranium ores may have both economic and environmental consequences. Particle-size redistribution of radium during milling has been demonstrated by previous investigators; however, the identification of sorbing components in the tailings has received little experimental attention. In this study, uranium-bearing sandstone ore was milled, on a laboratory scale, with sulfuric acid. At regular intervals, filtrate from this suspension was placed in contact with mixtures of quartz sand and various potential sorbents which occur as gangue in uranium ores; the potential sorbents included clay minerals, iron and aluminum oxides, feldspar, fluorspar, barite, jarosite, coal, and volcanic glass. After equilibration, the quartz sand-sorbent mixtures were separated from the filtrate and radioassayed by gamma-spectrometry to determine the quantities of 238U, 230Th, 226Ra, and 210Pb sorbed, and the radon emanation coefficients. Sorption of 238U was low in all cases, with maximal sorptions of 1-2% by the bentonite- and coal-bearing samples. 230Th sorption also was generally less than 1%; maximal sorption here was observed in the fluorspar-bearing sample and appears to be associated with the formation of gypsum during milling. 226Ra and 210 Pb generally showed higher sorption than the other nuclides - more than 60% of the 26Ra solubilized from the ore was sorbed on the barite-bearing sample. The mechanism (s) for this sorption by a wide variety of substrates is not yet understood. Radon emanation coefficients of the samples ranged from about 5 to 30%, with the coal-bearing samples clearly demonstrating an emanating power higher than any of the other materials. ?? 1990.

Zircon U-Pb geochronology and geochemistry of granites in the Zhuguangshan complex, South China: Implications for uranium mineralization

NASA Astrophysics Data System (ADS)

Zhang, Long; Chen, Zhenyu; Li, Xiaofeng; Li, Shengrong; Santosh, M.; Huang, Guolong

2018-05-01

The Zhuguangshan complex, composed of Caledonian, Indosinian, and Yanshanian granites, and Cretaceous mafic dykes, is one of the most important granite-hosted uranium producers in South China. Here we present LA-ICP-MS zircon U-Pb and hornblende 40Ar/39Ar geochronology and whole-rock and biotite geochemistry for the granites in this complex to evaluate the magmatism and its constraints on uranium mineralization. Samples collected from the Fuxi, Youdong, Longhuashan, Chikeng, Qiling, and Sanjiangkou intrusions yield zircon weighted 206Pb/238U ages of 426.7 ± 5.4 Ma, 226.4 ± 3.5 Ma, 225.0 ± 2.7 Ma, 152.2 ± 3.0 Ma, 153.9 ± 2.1 Ma, and 155.2 ± 2.1 Ma, respectively. A new Ar-Ar dating of the hornblende of the diabase from the Changjiang uranium ore field yields a plateau age of 145.1 ± 1.5 Ma. These results coupled with published geochronological data indicate that six major magmatic events occurred in the study area at 420-435 Ma, 225-240 Ma, 150-165 Ma, 140 Ma, 105 Ma, and 90 Ma. Both U-bearing and barren granites occur in this complex, and they display differences in whole-rock and biotite geochemistry. The barren granites show higher Al2O3, CaO, TFMM, Rb, Zr, Ba, SI, Mg#, (La/Yb)N, and Eu/Eu*, but lower SiO2, ALK, Rb, DI, Rb/Sr, and TiO2/MgO than those of the U-bearing granites. Biotites in the U-bearing granites are close to the Fe-rich siderophyllite-annite end member with Fe/(Fe + Mg) ratios higher than 0.66, whereas those in the barren granites are relatively close to the Mg-rich eastonite-phlogopite end member with Fe/(Fe + Mg) ratios <0.66. The U-bearing granites were mainly derived from the partial melting of pelitic sedimentary source, whereas the psammitic source generated the barren granites. In addition, the barren granites show higher TFMM, Ba, and Eu/Eu* but lower SiO2, Rb/Sr and Al2O3/TiO2 ratios with higher zircon saturation temperatures relative to the U-bearing granites. These results indicate that the geochemical compositions of the U-bearing and barren granites are dictated not only by the compositions of source rocks but also the physicochemical conditions of partial melting. Our study suggests that these two factors are also the major factors that control uranium ore potential of the granites in the Zhuguangshan complex. The geochemical variations of U-bearing and barren granites can serve as a potential detector for granite-hosted uranium deposits.

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

Balat, M.

The objective of this study is to determine the lignite use for Turkey's energy necessity. Lignite is the most important energy resource of Turkey when compared with others according to the amount of reserves. Lignite is the dominant source of energy produced (43%) in Turkey. Lignite deposits are encountered in almost every region of Turkey. Total lignite reserves are estimated at 8,375 million tons, of which 7,340 million tons (88%) is economically feasible. Share of lignite reserves of Turkey are 2% in the world. Lignite deposits are encountered in almost every region of Turkey. Afsin-Elbistan, Mugla, Soma, Tuncbilek, Seyitomer, Beypazarimore » and Sivas basins constitutes the most important known lignite reserves. The biggest lignite deposits, 40% of the total, are in Afsin-Elbistan. Lignite extraction is expected to increase as the government feels pressure to close down unprofitable hard coal mines that are geologically difficult, increasing the cost of extraction.« less

Stress-sensitivity of The Hydraulic Properties of A Fault Gouge

NASA Astrophysics Data System (ADS)

Harrington, J. F.; Horseman, S. T.; Hama, K.; Metcalfe, R.

Tono Mine is located about 350 km southwest of Tokyo and is the site of the most extensive uranium deposits in Japan. The geological setting comprises Tertiary (Mizu- nami Group) sedimentary rocks overlying Cretaceous granitic basement rocks. In as- cending order, the sedimentary rocks are the Toki Lignite-bearing Formation (con- glomerate, interbedded sandstone and mudstone), the Akeyo Formation (tuffaceous sandstone) and the Oidawara Formation (siltstone and mudstone). The Tsukiyoshi Fault cuts through this sequence and is a reverse fault, dipping to the south at 60- 70 degrees, with a throw of about 30 metres. As part of its hydrogeological studies, JNC is evaluating the impact of the fault on groundwater flow in the Tertiary sedi- ments. A sample was taken from a borehole in the NATM Drift, where the fault zone contains gouge material with two clay-bearing layers around 2 to 3 cm thick, separated by a 10 to 20 cm thick layer of unconsolidated fine sandy material. The sample was obtained using a triple-tube core barrel fitted with a split sample tube and a diamond bit. A specimen was prepared and consolidated at successive effective stress levels of 2, 6 and 12 MPa. The plot of void ratio against the logarithm of effective stress was found to be sensibly linear with a negative slope, kappa, of 0.036 rising to 0.044 at higher stress levels. The evidence suggests that the gouge is overconsolidated. Hy- draulic conductivity and specific storage were also measured at each stress level using the constant flow rate method. Hydraulic conductivity was found to be strongly stress sensitive, falling from 1.84 x 10-12 m.s-1 at 2 MPa to 7.9 x 10-14 m.s-1 at 12 MPa. Specific storage values were analysed using the critical state soil mechanics approach assuming a stress-dependent pore compressibility. Reasonable agreement was found between the theoretical curve with kappa = 0.036 and the measured values.

Removal of uranium from aqueous HF solutions

DOEpatents

Pulley, Howard; Seltzer, Steven F.

1980-01-01

This invention is a simple and effective method for removing uranium from aqueous HF solutions containing trace quantities of the same. The method comprises contacting the solution with particulate calcium fluoride to form uranium-bearing particulates, permitting the particulates to settle, and separting the solution from the settled particulates. The CaF.sub.2 is selected to have a nitrogen surface area in a selected range and is employed in an amount providing a calcium fluoride/uranium weight ratio in a selected range. As applied to dilute HF solutions containing 120 ppm uranium, the method removes at least 92% of the uranium, without introducing contaminants to the product solution.

Recovery of uranium values

DOEpatents

Brown, K. B.; Crouse, Jr., D. J.; Moore, J. G.

1959-03-10

A liquid-liquid extraction method is presented for recovering uranium values from an aqueous acidic solution by means of certain high molecular weight amine fn the amine classes of primary, secondary, heterocyclic secondary, tertiary, or heterocyclic tertiary. The uranium bearing aqueous acidic solution is contacted with the selected anine dissolved in a nonpolar waterimmiscible organfc solvent such as kerosene. The uranium which is substantially completely extracted by the organic phase may be stripped therefrom by water, and recovered from the aqueous phase by treatment into ammonia to precipitate ammonium diuranate.

RECOVERY OF URANIUM VALUES

DOEpatents

Brown, K.B.; Crouse, D.J. Jr.; Moore, J.G.

1959-03-10

A liquid-liquid extraction method is presented for recovering uranium values from an aqueous acidic solution by means of certain high molecular weight amine in the amine classes of primary, secondary, heterocyclic secondary, tertiary, or heterocyclic tertiary. The uranium bearing aqueous acidic solution is contacted with the selected amine dissolved in a nonpolar water-immiscible organic solvent such as kerosene. The uranium which is substantially completely exiracted by the organic phase may be stripped therefrom by waters and recovered from the aqueous phase by treatment into ammonia to precipitate ammonium diuranate.

Preliminary reconnaissance survey for thorium, uranium, and rare-earth oxides, Bear Lodge Mountains, Crook County, Wyoming

USGS Publications Warehouse

Wilmarth, V.R.; Johnson, D.H.

1953-01-01

An area about 6 miles north of Sundance, in the Bear Lodge Mountains, in Crook County, Wyo., was examined during August 1950 for thorium, uranium, and rare-earth oxides and samples were collected. Uranium is known to occur in fluorite veins and iron-manganese veins and in the igneous rocks of Tertiary age that compose the core of the Bear Lodge Mountains. The uranium content of the samples ranges from 0.001 to 0.015 percent in those from the fluorite veins, from 0.005 to 0.018 percent in those from the iron-manganese veins, and from 0.001 to 0.017 percent in those from the igneous rocks. The radioactivity of the samples is more than that expected from the uranium content. Thorium accounts for most of this discrepancy. The thorium oxide content of samples ranges from 0.07 to 0.25 percent in those from the iron-manganese veins and from 0.07 to 0.39 percent in those from the sedimentary rocks, and from0.04 to 0.30 in those from the igneous rocks. Rare-earth oxides occur in iron-manganese veins and in zones of altered igneous rocks. The veins contain from 0.16 to 12.99 percent rare-earth oxides, and the igneous rocks, except for two localities, contain from 0.01 to 0.42 percent rare-earth oxides. Inclusions of metamorphosed sedimentary rocks in the intrusive rocks contain from 0.07 to 2.01 percent rare-earth oxides.

Uranium and organic matters: use of pyrolysis-gas chromatography, carbon, hydrogen, and uranium contents to characterize the organic matter from sandstone-type deposits

USGS Publications Warehouse

Leventhal, Joel S.

1979-01-01

Organic matter seems to play an important role in the genesis of uranium deposits in sandstones in the western United States. Organic materials associated with ore from the Texas coastal plain, Tertiary basins of Wyoming, Grants mineral belt of New Mexico, and the Uravan mineral belt of Utah and Colorado vary widely in physical appearance and chemical composition. Partial characterization of organic materials is achieved by chemical analyses to determine atomic hydrogen-to-carbon (H/C) ratios and by gas chromatographic analyses to determine the molecular fragments evolved during stepwise pyrolysis. From the pyrolysis experiments the organic materials can be classified and grouped: (a) lignites from Texas and Wyoming and (b) hydrogen poor materials, from Grants and Uravan mineral belts and Wyoming; (c) naphthalene-containing materials from Grants mineral belt and Wyoming; and (d) complex and aromatic materials from Uravan, Grants and Wyoming. The organic materials analyzed have atomic H/C ratios that range from approximately 0.3 to at least 1.5. The samples with higher H/C ratios yield pyrolysis products that contain as many as 30 carbon atoms per molecule. Samples with low H/C ratios are commonly more uraniferous and yield mostly methane and low-molecular-weight gases during pyrolysis.

Aerial radiometric and magnetic reconnaissance survey of portions of Arizona, Idaho, Montana, New Mexico, South Dakota and Washington. Volume 2-F. Lewistown Quadrangle. Final report

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

Not Available

1979-06-01

Results of a high-sensitivity, aerial, gamma-ray spectrometer and magnetometer survey of the Lewistown Quadrangle, Montana, are presented. Instrumentation and methods are described in Volume 1 of this final report. Statistical and geological analysis of the radiometric data revealed 58 uranium anomalies worthy of field-checking as possible prospects. One anomaly may be associated with the Cambrian Flathead Quartzite that may contain deposits similar to the Blind River and Rand uranium deposits. Three anomalies may be indicative of sandstone-type deposits in Jurassic rocks, particularly the Morrison Formation, which hosts uranium mineralization elsewhere. One of the latter anomalies is also related to rocksmore » of the Mississippian Madison Group, and this suggests the possible presence of uranium in limestones of the Mission Canyon Formation. There are 45 anomalies related to the Cretaceous rocks. Lignite in the Hell Creek and Judith River formations and Eagle Sandstone may have caused the formation of 22 epigenetic uranium deposits. Many anomalies occur in the Bearpaw Shale and Claggett Formation. However, only five are considered significant of the remainder are expected to be caused by large amounts of radioactive bentonite or bentonitic shale. Two other Cretaceous units that may host sandstone-type deposits are the Colorado Shale and Kootenai Formation that register 16 and two anomalies respectively. Only one anomaly pertains to Tertiary rocks, and it may be indicative of vein-type deposits in the intrusives of the Judith Mountains. These rocks may also act as source rocks for deposits surrounding the Judith Mountains. Eight anomalies related only to Quaternary units may be demonstrative of uranium-rich source rocks that could host uranium mineralization.Several anomalies are located close to oil fields and may have been cause by radium-rich oil-field brines.« less

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

Buck, E.C.; Cunnane, J.C.; Brown, N.R.

A combination of optical microscopy, scanning electron microscopy with backscattered electron detection (SEM/BSE), and analytical electron microscopy (AEM) is being used to determine the nature of uranium in soils from the Fernald Environmental Management Project. The information gained from these studies is being used to develop and test remediation technologies. Investigations using SEM have shown that uranium is contained within particles that are typically 1 to 100 {mu}m in diameter. Further analysis with AEM has shown that these uranium-rich regions are made up of discrete uranium-bearing phases. The distribution of these uranium phases was found to be inhomogeneous at themore » microscopic level.« less

Occurrence of microbial acetate-oxidation in ~2 km-deep coal-bearing sediments off the Shimokita Peninsula, Japan (IODP Expedition 337)

NASA Astrophysics Data System (ADS)

Ijiri, A.; Inagaki, F.

2015-12-01

During the Integrated Ocean Drilling Program (IODP) Expedition 337 in 2012, the riser-drilling vessel Chikyu extended the previous world depth record of scientific ocean drilling and made one of the deepest scientific borehole down to 2466 m below the seafloor (mbsf) at Site C0020 Hole A off the Shimokita Peninsula, Japan. The sedimentary sequence consists of 17 lignite layers below 1.5 km bellow the seafloor. Microbiological and geochemical data consistently showed evidence for the existence of microbial communities associated with lignite coal beds in the coal-bearing sediments (Inagaki and Hinrichs et al., Science, 2015). Since lignite coals produce substantial dissolved organic compounds during the burial alternation process, volatile fatty acids may play important roles for microbial life and its activity in the deep sedimentary environment. To address this hypothesis, we measured methanogenic and acetate-oxidation activities by radiotracer incubation experiments using 14C-labelled substrate ([2-14C]-acetate) immediately after core recovery. Activity of aceticlastic methanogenesis was observed in the sediment above the coal-baring layers (>1990 mbsf), ranging from 0.2 to 1.2 pmol cm-3 d-1. The highest activity was observed in a coal-bed horizon at 1990 mbsf. However, aceticlastic methanogenesis was below the detection limit in sediment samples below the 2 km-coal layers. Activity of acetate oxidation to CO2 was measured by 14CO2 production rate from [2-14C]-acetate. Interestingly, the acetate-oxidation activity was observed in sediments above the coal beds, which values were generally higher than those of methanogenesis with the maximum value of 33 pmol cm-3 d-1 at 1800 mbsf. The rates gradually decreased with increasing depth from 1800 mbsf and reached below the detection limit (i.e., 0.05 pmol cm-3 d-1) in 2 km-deep coal-bed samples. The occurrence of relatively high acetate oxidation at ~1800 mbsf above the coal formation suggests that microbes respire acetate with available electron acceptors such as glauconitic iron oxides in the deep sedimentary environment.

The Gas Hills uranium district and some probable controls for ore deposition

USGS Publications Warehouse

Zeller, Howard Davis

1957-01-01

Uranium deposits occur in the upper coarse-grained facies of the Wind River formation of Eocene age in the Gas Hills district of the southern part of the Wind River Basin. Some of the principal deposits lie below the water table in the unoxidized zone and consist of uraninite and coffinite occurring as interstitial fillings in irregular blanket-like bodies. In the near-surface deposits that lie above the water table, the common yellow uranium minerals consist of uranium phosphates, silicates, and hydrous oxides. The black unoxidized uraninite -coffinite ores show enrichment of molybdenum, arsenic, and selenium when compared to the barren sandstone. Probable geologic controls for ore deposits include: 1) permeable sediments that allowed passage of ore-bearing solutions; 2) numerous faults that acted as impermeable barriers impounding the ore -bearing solutions; 3) locally abundant pyrite, carbonaceous material, and natuial gas containing hydrogen sulfide that might provide a favorable environment for precipitation of uranium. Field and laboratory evidence indicate that the uranium deposits in the Gas Hills district are very young and related to the post-Miocene to Pleistocene regional tilting to the south associated with the collapse of the Granite Mountains fault block. This may have stopped or reversed ground water movement from a northward (basinward) direction and alkaline ground water rich in carbonate could have carried the uranium into the favorable environment that induced precipitation.

Impact of the uranium (VI) speciation in mineralised urines on its extraction by calix[6]arene bearing hydroxamic groups used in chromatography columns.

PubMed

Baghdadi, S; Bouvier-Capely, C; Ritt, A; Peroux, A; Fevrier, L; Rebiere, F; Agarande, M; Cote, G

2015-11-01

Actinides determination in urine samples is part of the analyses performed to monitor internal contamination in case of an accident or a terrorist attack involving nuclear matter. Mineralisation is the first step of any of these analyses. It aims at reducing the sample volume and at destroying all organic compounds present. The mineralisation protocol is usually based on a wet ashing step, followed by actinides co-precipitation and a furnace ashing step, before redissolution and the quantification of the actinides by the appropriate techniques. Amongst the existing methods to perform the actinides co-precipitation, alkali-earth (typically calcium) precipitation is widely used. In the present work, the extraction of uranium(VI), plutonium(IV) and americium(III) from the redissolution solutions (called "mineralised urines") on calix[6]arene columns bearing hydroxamic groups was investigated as such an extraction is a necessary step before their determination by ICP-MS or alpha spectrometry. Difficulties were encountered in the transfer of uranium(VI) from raw to mineralised urines, with yield of transfer ranging between 0% and 85%, compared to about 90% for Pu and Am, depending on the starting raw urines. To understand the origin of such a difficulty, the speciation of uranium (VI) in mineralised urines was investigated by computer simulation using the MEDUSA software and the associated HYDRA database, compiled with recently published data. These calculations showed that the presence of phosphates in the "mineralised urines" leads to the formation of strong uranyl-phosphate complexes (such as UO2HPO4) which compete with the uranium (VI) extraction by the calix[6]arene bearing hydroxamic groups. The extraction constant of uranium (VI) by calix[6]arene bearing hydroxamic groups was determined in a 0.04 mol L(-1) sodium nitrate solution (logK=4.86±0.03) and implemented in an extraction model taking into account the speciation in the aqueous phase. This model allowed to simulate satisfactorily the experimental uranium extraction data and to support the preliminary conclusions about the role of the phosphates present in mineralised urines. These calculations also showed that the phosphate/calcium ratio is a key parameter as far as the efficiency of the uranium (VI) extraction by the calix[6]arene columns is concerned. It predicted that the addition of CaCl2 in mineralised urines would release uranium (VI) from phosphates by forming calcium (II)-phosphate complexes and thus facilitate the uranium (VI) extraction on calix[6]arene columns. These predictions were confirmed experimentally as the addition of 0.1 mol L(-1) CaCl2 to a mineralised urine containing naturally a high concentration of phosphate (typically 0.04 mol L(-1)) significantly increased the percentage of uranium (VI) extraction on the calix[6]arene columns. Copyright © 2015 Elsevier B.V. All rights reserved.

Microbial screening test for lignite degradation: Quarterly progress report No. 9 for the period January-March 1987

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

Yen, Teh Fu

1987-03-01

Anaerobic fermentation of water soluble fraction of modified lignite was attempted. Solubilized lignite formed bioprecipitate after biodegradation. Fermentation of water solubilized lignite in enrichment media produced gases and organic acids. FT-IR spectra of solubilized lignite after biodegradation showed that the concentration of organic oxygen have decreased and that the concentration of -CH/sub 3/ terminal group have increased. Solubilized lignite may serve as sole carbon source by using selective media. Bacteria was suspected of being able to utilize fulvic-like materials from solubilized lignite. Isolation of anaerobic bacteria was achieved by surface culture, and it indicated morphological differences among isolated colonies. Alginatemore » gel entrapment, an immobilization method, was applied to T. versicolor fungal cells. Active fungal growth was observed from the immobilized spheres on sodium-alginate gel. It seems that the immobilized biocatalysts may be used to enhance the production of bioextract from lignite in a reactor system. Hydroxylation of lignite was accomplished through Fenton reaction at pH 7.5. FT-IR analysis showed that lignite treated with Fenton's reagent exhibits weaker aromatic bending and ether linkage than untreated lignite. 13 refs., 8 figs.« less

Reconnaissance for uranium in the coal of Sao Paulo, Santa Catarina, and Rio Grande do Sul, Brazil

USGS Publications Warehouse

Haynes, Donald D.; Pierson, Charles T.; White, Max G.

1958-01-01

Uranium-bearing coal and carbonaceous shale of the Rio Bonito formation of Pennsylvanian age have been found in the States of Sao Paulo, Santa Catarlna and Rio Grande do Sul, Brazil. The uranium oxide content of the samples collected in the State of Sao Paulo ranges from 0.001 percent to 0.082 percent. The samples collected in Santa Catarina averaged about 0.002 percent uranium oxide; those collected in Rio Grande do Sul, about 0.003 percent uranium oxide. Since the field and laboratory investigations are still in their initial stages, only raw data on the radioactivity and uranium content of Brazilian coals are given in this report.

Uranium deposits at the Jomac mine, White Canyon area, San Juan County, Utah

USGS Publications Warehouse

Trites, A.F.; Hadd, G.A.

1955-01-01

azurite, and chalcanthite occur locally with the uranium minerals. Principal ore guides at the Jomac mine are channels, and scours at the bottom of these channels coal-bearing sandstone or conglomerate at the base of the Shinarump conglomerate, coal, and jarosite.

A preliminary report on a zone containing thick lignite beds, Denver Basin, Colorado

USGS Publications Warehouse

Soister, Paul E.

1973-01-01

A zone of lignite beds of Paleocene age in the Denver Formation (Upper Cretaceous and Paleocene) lies about 800-1,500 feet above the well-known and extensively mined coal beds of the Laramie Formation (Upper Cretaceous). The zone is a few hundred to as much as 500 feet thick. Where lignite beds lie within 1,000 feet of the surface, this zone underlies an area about 30 miles wide by about 75 miles long, stretching from just northeast of Denver to several miles south of Calhan. Fifteen mines were operated at various periods between 1874 and 1940 and probably produced a total of less than 100,000 tons of lignite, mostly for local use. From 1874 to 1974, several geologists have reported on this lignite zone or the enclosing beds, but no detailed reports have been written except for one by this writer. Drill holes are the main source of geologic data, owing to poor exposure. There are generally about 3 to 6 lignite beds, and they are mostly about 15 or 20 to a few tens of feet apart. Most or all beds typically contain numerous non-coal partings from a fraction of an inch to several inches thick, so that thickness of lignite beds should be stated as gross thickness and as net lignite thickness; net lignite thickness is generally from 70 to 90 percent of gross thickness. Many partings are composed of kaolin, but others are composed of other clay minerals, siltstone, and sandstone. The lignite beds range generally from 1 or 2 to several feet thick, and some are as much as 10-25 feet thick; the thickest known bed has a maximum thickness of 54.5 feet, with a net lignite thickness of 40 feet. Most lignite beds seem to have fair lateral continuity, and at least some beds are several miles in extent. The thickest known lignite bed was traced for at least 18 miles, from northwest to southeast of Watkins. The lignite is brownish-black to black, weathers, checks, and disintegrates rapidly, and even in drill cores from a few hundred feet in depth the lignite is easily broken by hand pressure. Quality of the lignite is lowered by the non-coal partings and, locally at least, by some small blebs and balls of clay in the lignite itself, especially at the base. Available analyses indicate that the following general figures, on an as-received basis, may be applied to relatively clean lignite from this zone: 6,000-7,000 Btu, 20-35 percent moisture, 8-18 percent ash, and 0.3-0.5 percent sulfur. Rank of the lignite is lignite A as calculated by the formulas of the American Society for Testing and . Materials (ASTM), although some parts, especially of deeper beds, may be as high as subbituminous C coal in rank. Best utilization of the lignite probably would be by gasification, liquefaction, or similar methods, because of the numerous non-coal partings and low quality. The thickest known lignite bed is estimated to contain at least 1.25 billion short tons of lignite. Two methods of roughly estimating the order of magnitude of lignite resources, in beds at least 4 feet thick and within 1,000 feet of the surface in this zone, indicate resources are on the order of 20 billion tons.

The distribution of trace elements in Turkish lignites in Western Anatolia and the Thrace Basin

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

Palmer, C.A.; Tuncali, E.; Finkelman, R.

1999-07-01

The United States Geological Survey (USGS) and the General Directorate of Mineral Research and Exploration in Turkey (Maden Tetkik ve Arama:MTA) are working together to provide a more complete understanding of the chemical properties of lignites from major Turkish lignite producing areas. The project is a part of the USGS effort to produce an international coal database and is part of the ``Technological and Chemical properties of Turkish Lignite Inventory Project'' being conducted by the MTA General Directorate. The lignites in Turkey formed in several different depositional environments at different geologic times and have differing chemical properties. The Eocene lignitesmore » are limited to northern Turkey. Oligocene lignites, in the Trace Basin of northwestern Turkey, are intercalated with marine sediments. Miocene lignites are generally located in western Turkey. These coal deposits have relatively abundant reserves, with limnic characteristics. The Pliocene-Pleistocene lignites are found in the eastern part of Turkey. Most of these lignites have low calorific values, high moisture and high ash contents. The majority of the lignite extraction is worked in open-pit mines. Turkish lignite production is used mainly by power plants; small amounts are used by households and in industry. All the samples in this study were collected as channel samples of the beds. Analyses of 71 coal samples (mostly lignites) have been completed for 54 elements using various analytical techniques including inductively coupled plasma emission and mass spectrometry, instrumental neutron activation analysis and various single element techniques. Many of these lignites have elemental concentrations similar to those of US lignites. However, maximum or mean concentrations of B, Cr, Cs, Ni, As, Br, Sb, Cs and U in Turkey were higher than the corresponding maximum or mean found in either of the Fort Union or Gulf Coast basins, the two most productive lignite basins in the U.S.« less

Wettability modification of Wender lignite by adsorption of dodecyl poly ethoxylated surfactants with different degree of ethoxylation: A molecular dynamics simulation study.

PubMed

Zhang, Lei; Li, Bao; Xia, Yangchao; Liu, Shengyu

2017-09-01

Lignite is an important and useful fossil fuel in the world and the strong hydrophilicity of it limits its applications. Surfactant adsorption on lignite is an effective way to make it hydrophobic. In this work, aiming to examine the effect of the degree of ethoxylation on the adsorption behavior of dodecyl poly ethoxylated surfactants on lignite and the wettability modification of modified lignite by surfactant adsorption, different combined systems formed by surfactants, water and a model surface of Wender lignite have been studied using molecular dynamics simulation. The adsorption configurations vary with the degree of ethoxylation. At the same adsorption amounts, increasing the degree of ethoxylation can make the adsorption layer more compactness and bring stronger adsorption strength. The results of binding energy and its components show that the adsorption of alkyl polyoxyethylene ethers surfactant on lignite is physically adsorbed rather than electrostatically or chemisorbed. Meanwhile, van der Waals interaction plays a dominant role in the adsorption. The addition of surfactant could reduce the possibility of the interaction between water and lignite. Compared to the original lignite, the interaction between them is weakened after surfactant adsorption in water/surfactant/lignite system, thus strengthening the hydrophobicity of lignite. Similar to the adsorption strength, hydrophobicity of modified lignite increases with the increase of the degree of ethoxylation. The lignite surface properties are changed due to surfactant adsorption by analyzing the compositions of interaction energy and the change of hydrogen bonds. Copyright © 2017 Elsevier Inc. All rights reserved.

Lignite pellets and methods of agglomerating or pelletizing

DOEpatents

Baker, Albert F.; Blaustein, Eric W.; Deurbrouck, Albert W.; Garvin, John P.; McKeever, Robert E.

1981-01-01

The specification discloses lignite pellets which are relatively hard, dust resistant, of generally uniform size and free from spontaneous ignition and general degradation. Also disclosed are methods for making such pellets which involve crushing as mined lignite, mixing said lignite with a binder such as asphalt, forming the lignite binder mixture into pellets, and drying the pellets.

Microbial screening test for lignite degradation. Quarterly progress report No. 1, January-March 1985

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

Yen, T.F.

1985-01-01

Potassium permanganate and sodium hypochlorite oxidation of lignitic coal were performed. Ion chromatography of low molecular weight carboxylic acids - oxalic acid, formic acid, and acetic acid - produced by potassium permanganate and sodium hypochlorite oxidation was executed. Oxalic acid was found to be the most predominant low molecular weight species. It was estimated that about 10% of the carbon present in the chemical structure of lignite was converted to oxalic acid by sodium hypochlorite oxidation. Ion chromatography analysis showed that about 43% of the lignite carbon was converted to carbon dioxide in all experiments. Biological degradation of lignite bymore » P. versicolor, a white-rot fungus, on lignite/agar and lignite slurry was attempted. Apparently, P. versicolor is capable of growing on lignite slurry. Acclimation of P. versicolor to lignite was proceeded. Biochemical reaction test for laccase production of P. versicolor was performed and found to be positive. 15 refs., 5 figs., 6 tabs.« less

Distribution and correlation of the natural radionuclides in a coal mine of the West Macedonia Lignite Center (Greece).

PubMed

Tsikritzis, L I; Fotakis, M; Tzimkas, N; Kolovos, N; Tsikritzi, R

2008-02-01

The distribution and correlation of six natural nuclides in the West Macedonia Lignite Center, Northern Greece were studied. Fifty-five samples of lignite, aged from 1.8 to 5 million years, and corresponding steriles, beds of marls, clays and sands alternating with the lignite, were collected perpendicular to the mine benches and measured spectroscopically. The mean concentrations of (238)U and (226)Ra in lignites were found to be higher than that in steriles since these nuclides are associated with the organic material of lignite, whereas (238)U/(226)Ra equilibrium was not observed in either lignites or steriles. Finally, the ratio (226)Ra/(228)Ra in lignites was approximately double of that in steriles, confirming the affinity of the (238)U series with the coal matrix in contrast to the (232)Th series. No correlation was found between radionuclide concentrations and the depth of the sample, nor with the ash content of lignite.

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

Yilmaz, A.O.

Total coal reserve (hard coal + lignite) in the world is 984 billion tons. While hard coal constitutes 52% of the total reserve, lignite constitutes 48% of it. Turkey has only 0.1% of world hard coal reserve and 1.5% of world lignite reserves. Turkey has 9th order in lignite reserve, 8th order in lignite production, and 12th order in total coal (hard coal and lignite) consumption. While hard coal production meets only 13% of its consumption, lignite production meets lignite consumption in Turkey. Sixty-five percent of produced hard coal and 78% of produced lignite are used for electricity generation. Lignitesmore » are generally used for electricity generation due to their low quality. As of 2003, total installed capacity of Turkey was 35,587 MW, 19% (6,774 MW) of which is produced from coal-based thermal power plants. Recently, use of natural gas in electricity generation has increased. While the share of coal in electricity generation was about 50% for 1986, it is replaced by natural gas today.« less

SLURRY SOLVENT EXTRACTION PROCESS FOR THE RECOVERY OF METALS FROM SOLID MATERIALS

DOEpatents

Grinstead, R.R.

1959-01-20

A solvent extraction process is described for recovering uranium from low grade uranium bearing minerals such as carnotit or shale. The finely communited ore is made up as an aqueous slurry containing the necessary amount of acid to solubilize the uranium and simultaneously or subsequently contacted with an organic solvent extractant such as the alkyl ortho-, or pyro phosphoric acids, alkyl phosphites or alkyl phosphonates in combination with a diluent such as kerosene or carbon tetrachlorids. The extractant phase is separated from the slurry and treated by any suitable process to recover the uranium therefrom. One method for recovering the uranium comprises treating the extract with aqueous HF containing a reducing agent such as ferrous sulfate, which reduces the uranium and causes it to be precipitated as uranium tetrafluoride.

Hydrothermal uranium deposits containing molybdenum and fluorite in the Marysvale volcanic field, west-central Utah

USGS Publications Warehouse

Cunningham, C.G.; Rasmussen, J.D.; Steven, T.A.; Rye, R.O.; Rowley, P.D.; Romberger, S.B.; Selverstone, J.

1998-01-01

Uranium deposits containing molybdenum and fluorite occur in the Central Mining Area, near Marysvale, Utah, and formed in an epithermal vein system that is part of a volcanic/hypabyssal complex. They represent a known, but uncommon, type of deposit; relative to other commonly described volcanic-related uranium deposits, they are young, well-exposed and well-documented. Hydrothermal uranium-bearing quartz and fluorite veins are exposed over a 300 m vertical range in the mines. Molybdenum, as jordisite (amorphous MoS2, together with fluorite and pyrite, increase with depth, and uranium decreases with depth. The veins cut 23-Ma quartz monzonite, 20-Ma granite, and 19-Ma rhyolite ash-flow tuff. The veins formed at 19-18 Ma in a 1 km2 area, above a cupola of a composite, recurrent, magma chamber at least 24 ?? 5 km across that fed a sequence of 21- to 14-Ma hypabyssal granitic stocks, rhyolite lava flows, ash-flow tuffs, and volcanic domes. Formation of the Central Mining Area began when the intrusion of a rhyolite stock, and related molybdenite-bearing, uranium-rich, glassy rhyolite dikes, lifted the fractured roof above the stock. A breccia pipe formed and relieved magmatic pressures, and as blocks of the fractured roof began to settle back in place, flat-lying, concave-downward, 'pull-apart' fractures were formed. Uranium-bearing, quartz and fluorite veins were deposited by a shallow hydrothermal system in the disarticulated carapace. The veins, which filled open spaces along the high-angle fault zones and flat-lying fractures, were deposited within 115 m of the ground surface above the concealed rhyolite stock. Hydrothermal fluids with temperatures near 200??C, ??18OH2O ~ -1.5, ?? -1.5, ??DH2O ~ -130, log fO2 about -47 to -50, and pH about 6 to 7, permeated the fractured rocks; these fluids were rich in fluorine, molybdenum, potassium, and hydrogen sulfide, and contained uranium as fluoride complexes. The hydrothermal fluids reacted with the wallrock resulting in precipitation of uranium minerals. At the deepest exposed levels, wall-rocks were altered to sericite; and uraninite, coffinite, jordisite, fluorite, molybdenite, quartz, and pyrite were deposited in the veins. The fluids were progressively oxidized and cooled at higher levels in the system by boiling and degassing; iron-bearing minerals in wall rocks were oxidized to hematite, and quartz, fluorite, minor siderite, and uraninite were deposited in the veins. Near the ground surface, the fluids were acidified by condensation of volatiles and oxidation of hydrogen sulfide in near-surface, steam-heated, ground waters; wall rocks were altered to kaolinite, and quartz fluorite, and uraninite were deposited in veins. Secondary uranium minerals, hematite, and gypsum formed during supergene alteration later in the Cenozoic when the upper part of the mineralized system was exposed by erosion.

Behavior of uranium under conditions of interaction of rocks and ores with subsurface water

NASA Astrophysics Data System (ADS)

Omel'Yanenko, B. I.; Petrov, V. A.; Poluektov, V. V.

2007-10-01

The behavior of uranium during interaction of subsurface water with crystalline rocks and uranium ores is considered in connection with the problem of safe underground insulation of spent nuclear fuel (SNF). Since subsurface water interacts with crystalline rocks formed at a high temperature, the mineral composition of these rocks and uranium species therein are thermodynamically unstable. Therefore, reactions directed toward the establishment of equilibrium proceed in the water-rock system. At great depths that are characterized by hindered water exchange, where subsurface water acquires near-neutral and reducing properties, the interaction is extremely sluggish and is expressed in the formation of micro- and nanoparticles of secondary minerals. Under such conditions, the slow diffusion redistribution of uranium with enrichment in absorbed forms relative to all other uranium species is realized as well. The products of secondary alteration of Fe- and Ti-bearing minerals serve as the main sorbents of uranium. The rate of alteration of minerals and conversion of uranium species into absorbed forms is slow, and the results of these processes are insignificant, so that the rocks and uranium species therein may be regarded as unaltered. Under reducing conditions, subsurface water is always saturated with uranium. Whether water interacts with rock or uranium ore, the equilibrium uranium concentration in water is only ≤10-8 mol/l. Uraninite ore under such conditions always remains stable irrespective of its age. The stability conditions of uranium ore are quite suitable for safe insulation of SNF, which consists of 95% uraninite (UO2) and is a confinement matrix for all other radionuclides. The disposal of SNF in massifs of crystalline rocks at depths below 500 m, where reducing conditions are predominant, is a reliable guarantee of high SNF stability. Under oxidizing conditions of the upper hydrodynamic zone, the rate of interaction of rocks with subsurface water increases by orders of magnitude and subsurface water is commonly undersaturated with uranium. Uranium absorbed by secondary minerals, particularly by iron hydroxides and leucoxene, is its single stable species under oxidizing conditions. The impact of oxygen-bearing water leads to destruction of uranium ore. This process is realized simultaneously at different hypsometric levels even if the permeability of the medium is variable in both the lateral and vertical directions. As a result, intervals containing uranyl minerals and relics of primary uranium ore are combined in ore-bearing zones with intervals of completely dissolved uranium minerals. A wide halo of elevated uranium contents caused by sorption is always retained at the location of uranium ore entirely destroyed by weathering. Uranium ore commonly finds itself in the aeration zone due to technogenic subsidence of the groundwater table caused by open-pit mining or pumping out of water from underground mines. The capillary and film waters that interact with rocks and ores in this zone are supplemented by free water filtering along fractures when rain falls or snow is thawing. The interaction of uranium ore with capillary water results in oxidation of uraninite, accompanied by loosening of the mineral surface, formation of microfractures, and an increase in solubility with enrichment of capillary water in uranium up to 10-4 mol/l. Secondary U(VI) minerals, first of all, uranyl hydroxides and silicates, replace uraninite, and uranium undergoes local diffusion redistribution with its sorption by secondary minerals of host rocks. The influx of free water facilitates the complete dissolution of primary and secondary uranium minerals, the removal of uranium at the sites of groundwater discharge, and its redeposition under reducing conditions at a greater depth. It is evident that the conditions of the upper hydrodynamic zone and the aeration zone are unfit for long-term insulation of SNF and high-level wastes because, after the failure of containers, the leakage of radionuclides into the environment becomes inevitable.

Enhanced fuel production in thorium/lithium hybrid blankets utilizing uranium multipliers

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

Pitulski, R.H.

1979-10-01

A consistent neutronics analysis is performed to determine the effectiveness of uranium bearing neutron multiplier zones on increasing the production of U/sup 233/ in thorium/lithium blankets for use in a tokamak fusion-fission hybrid reactor. The nuclear performance of these blankets is evaluated as a function of zone thicknesses and exposure by using the coupled transport burnup code ANISN-CINDER-HIC. Various parameters such as U/sup 233/, Pu/sup 239/, and H/sup 3/ production rates, the blanket energy multiplication, isotopic composition of the fuels, and neutron leakages into the various zones are evaluated during a 5 year (6 MW.y.m/sup -2/) exposure period. Although themore » results of this study were obtained for a tokomak magnetic fusion device, the qualitative behavior associated with the use of the uranium bearing neutron multiplier should be applicable to all fusion-fission hybrids.« less

The Feed Materials Program of the Manhattan Project: A Foundational Component of the Nuclear Weapons Complex

NASA Astrophysics Data System (ADS)

Reed, B. Cameron

2014-12-01

The feed materials program of the Manhattan Project was responsible for procuring uranium-bearing ores and materials and processing them into forms suitable for use as source materials for the Project's uranium-enrichment factories and plutonium-producing reactors. This aspect of the Manhattan Project has tended to be overlooked in comparison with the Project's more dramatic accomplishments, but was absolutely vital to the success of those endeavors: without appropriate raw materials and the means to process them, nuclear weapons and much of the subsequent cold war would never have come to pass. Drawing from information available in Manhattan Engineer District Documents, this paper examines the sources and processing of uranium-bearing materials used in making the first nuclear weapons and how the feed materials program became a central foundational component of the postwar nuclear weapons complex.

Geological and geochemical aspects of uranium deposits. A selected, annotated bibliography

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

Garland, P.A.; Thomas, J.M.; Brock, M.L.

1980-06-01

A bibliography of 479 references encompassing the fields of uranium and thorium geochemistry and mineralogy, geology of uranium deposits, uranium mining, and uranium exploration techniques has been compiled by the Ecological Sciences Information Center of Oak Ridge National Laboratory. The bibliography was produced for the National Uranium Resource Evaluation Program, which is funded by the Grand Junction Office of the Department of Energy. The references contained in the bibliography have been divided into the following eight subject categories: (1) geology of deposits, (2) geochemistry, (3) genesis O deposits, (4) exploration, (5) mineralogy, (6) uranium industry, (7) reserves and resources, andmore » (8) geology of potential uranium-bearing areas. All categories specifically refer to uranium and thorium; the last category contains basic geologic information concerning areas which the Grand Junction Office feels are particularly favorable for uranium deposition. The references are indexed by author, geographic location, quadrangle name, geoformational feature, taxonomic name, and keyword.« less

Sustainable Mining Land Use for Lignite Based Energy Projects

NASA Astrophysics Data System (ADS)

Dudek, Michal; Krysa, Zbigniew

2017-12-01

This research aims to discuss complex lignite based energy projects economic viability and its impact on sustainable land use with respect to project risk and uncertainty, economics, optimisation (e.g. Lerchs and Grossmann) and importance of lignite as fuel that may be expressed in situ as deposit of energy. Sensitivity analysis and simulation consist of estimated variable land acquisition costs, geostatistics, 3D deposit block modelling, electricity price considered as project product price, power station efficiency and power station lignite processing unit cost, CO2 allowance costs, mining unit cost and also lignite availability treated as lignite reserves kriging estimation error. Investigated parameters have nonlinear influence on results so that economically viable amount of lignite in optimal pit varies having also nonlinear impact on land area required for mining operation.

Leaching of uranium from glass and ceramic foodware and decorative items

USGS Publications Warehouse

Landa, Edward R.; Councell, Terry B.

1992-01-01

Beginning as early as the first century A. D. and continuing until at least the 1970s, uranium was used as a coloring agent in glass and in ceramic glazes. The leaching of uranium from such items is of interest as some were designed for food storage or serving. Thirty-three glass items and two ceramic items were leached sequentially with deionized water, dilute acetic acid, and 1 M nitric acid to assess realistic and worst-case scenario leaching by foods and beverages. The maximum quantity of uranium leached from the uranium-bearing glasses was about 30 µg L-1, while that from the ceramic-glazed items was about 300,000 µg L-1.

Geological and geochemical aspects of uranium deposits: a selected, annotated bibliography. [474 references

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

Thomas, J.M.; Garland, P.A.; White, M.B.

This bibliography, a compilation of 474 references, is the fourth in a series compiled from the National Uranium Resource Evaluation (NURE) Bibliographic Data Base. This data base was created for the Grand Junction Office of the Department of Energy's National Uranium Resource Evaluation Project by the Ecological Sciences Information Center, Oak Ridge National Laboratory. The references in the bibliography are arranged by subject category: (1) geochemistry, (2) exploration, (3) mineralogy, (4) genesis of deposits, (5) geology of deposits, (6) uranium industry, (7) geology of potential uranium-bearing areas, and (8) reserves and resources. The references are indexed by author, geographic location,more » quadrangle name, geoformational feature, and keyword.« less

Future of lignite resources: a life cycle analysis.

PubMed

Wang, Qingsong; Liu, Wei; Yuan, Xueliang; Zheng, Xiaoning; Zuo, Jian

2016-12-01

Lignite is a low-quality energy source which accounts for 13 % of China's coal reserves. It is imperative to improve the quality of lignite for large-scale utilization. To further explore and analyze the influence of various key processes on the environment and economic costs, a lignite drying and compression technology is evaluated using an integrated approach of life cycle assessment and life cycle costs. Results showed that lignite mining, direct air emissions, and electricity consumption have most significant impacts on the environment. An integrated evaluation of life cycle assessment and life cycle costs showed that the most significant contributor to the environmental impacts and economic costs was the lignite mining process. The impact of transportation and wastewater treatment process on the environment and economic costs was small enough to be ignored. Critical factors were identified for reducing the environmental and economic impacts of lignite drying and compression technology. These findings provide useful inputs for both industrial practice and policy making for exploitation, processing, and utilization of lignite resources.

Pelletizing lignite

DOEpatents

Goksel, Mehmet A.

1983-11-01

Lignite is formed into high strength pellets having a calorific value of at least 9,500 Btu/lb by blending a sufficient amount of an aqueous base bituminous emulsion with finely-divided raw lignite containing its inherent moisture to form a moistened green mixture containing at least 3 weight % of the bituminous material, based on the total dry weight of the solids, pelletizing the green mixture into discrete green pellets of a predetermined average diameter and drying the green pellets to a predetermined moisture content, preferrably no less than about 5 weight %. Lignite char and mixture of raw lignite and lignite char can be formed into high strength pellets in the same general manner.

PROCESS FOR THE RECOVERY AND PURIFICATION OF URANIUM DEPOSITS

DOEpatents

Carter, J.M.; Kamen, M.D.

1958-10-14

A process is presented for recovering uranium values from UCl/sub 4/ deposits formed on calutrons. Such deposits are removed from the calutron parts by an aqueous wash solution which then contains the uranium values in addition to the following impurities: Ni, Cu, Fe, and Cr. This impurity bearing wash solution is treated with an oxidizing agent, and the oxidized solution is then treated with ammonia in order to precipitate the uranium as ammonium diuranate. The metal impurities of iron and chromium, which form insoluble hydroxides, are precipitated along with the uranium values. The precipitate is separated from the solution, dissolved in acid, and the solution again treated with ammonia and ammonium carbonate, which results in the precipitation of the metal impurities as hydroxides while the uranium values remain in solution.

Identification of Uranium Minerals in Natural U-Bearing Rocks Using Infrared Reflectance Spectroscopy

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

Beiswenger, Toya N.; Gallagher, Neal B.; Myers, Tanya L.

The identification of minerals, including uranium-bearing minerals, is traditionally a labor-intensive-process using x-ray diffraction (XRD), fluorescence, or other solid-phase and wet chemical techniques. While handheld XRD and fluorescence instruments can aid in field identification, handheld infrared reflectance spectrometers can also be used in industrial or field environments, with rapid, non-destructive identification possible via spectral analysis of the solid’s reflectance spectrum. We have recently developed standard laboratory measurement methods for the infrared (IR) reflectance of solids and have investigated using these techniques for the identification of uranium-bearing minerals, using XRD methods for ground-truth. Due to the rich colors of such species,more » including distinctive spectroscopic signatures in the infrared, identification is facile and specific, both for samples that are pure or are partially composed of uranium (e.g. boltwoodite, schoepite, tyuyamunite, carnotite, etc.) or non-uranium minerals. The method can be used to detect not only pure and partial minerals, but is quite sensitive to chemical change such as hydration (e.g. schoepite). We have further applied statistical methods, in particular classical least squares (CLS) and multivariate curve resolution (MCR) for discrimination of such uranium minerals and two uranium pure chemicals (U3O8 and UO2) against common background materials (e.g. silica sand, asphalt, calcite, K-feldspar) with good success. Each mineral contains unique infrared spectral features; some of the IR features are similar or common to entire classes of minerals, typically arising from similar chemical moieties or functional groups in the minerals: phosphates, sulfates, carbonates, etc. These characteristic 2 infrared bands generate the unique (or class-specific) bands that distinguish the mineral from the interferents or backgrounds. We have observed several cases where the chemical moieties that provide the spectral discrimination in the longwave IR do so by generating upward-going reststrahlen bands in the reflectance data, but the same minerals have other weaker (overtone) bands, sometimes from the same chemical groups, that are manifest as downward-going transmission-type features in the midwave and shortwave infrared.« less

Microbial screening test for lignite degradation. Quarterly progress report No. 4, October-December 1985

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

Yen, T.F.

1985-01-01

Chemical oxidation of lignite by means of hydrogen peroxide - acetic acid was executed. Methanol fractionation of the oxidized product yielded 76.4% methanol solubles, 9.3% methanol insolubles and 11.2% CO/sub 2/. Biodegradation of the methanol fraction by soil bacteria was found to be positive as demonstrated by gel permeation chromatography (GPC). The shift of the average molecular weight throughout biodegradation was estimated to be from 310 g/mole, to 243 g/mole, zero day and four weeks respectively. Biodegradation of lignitic substrates, benzene - methanol fraction (A - 1), aqueous alkaline fraction (A - 2), clean lignite residue (A - 3), rawmore » lignite, and methanol soluble fraction after oxidation, by means of oil - field soil bacteria and Polyporus versicolor ATCC 12679 was attempted. All previous mentioned lignitic substrates yielded positive results for oil-field soil bacteria, while A - 2 fraction and raw lignite yielded positive results for P. versicolor. Unidentified fungi strains, N 1, L 1, and L 2 were also tested on lignitic substrates. Mild growth was observed in these cases.« less

238U and 235U isotope fractionation upon oxidation of uranium-bearing rocks by fracture waters

NASA Astrophysics Data System (ADS)

Chernyshev, I. V.; Golubev, V. N.; Chugaev, A. V.; Mandzhieva, G. V.

2016-10-01

The variations in 238U/235U values accompanying mobilization of U by fracture waters from uranium-bearing rocks, in which U occurs as a fine impregnation of oxides and silicates, were studied by the high-precision (±0.07‰) MC-ICP-MS method. Transition of U into the aqueous phase in the oxidized state U(VI) is accompanied by its isotope fractionation with enrichment of dissolved U(VI) in the heavy isotope 238U up to 0.32‰ in relation to the composition of the solid phases. According to the sign, this effect is consistent with the tendency of the behavior of 238U and 235U upon interaction of river waters with rocks of the catchment areas [11] and with the effect observed during oxidation of uraninite by the oxygen-bearing NaHCO3 solution [12].

Biodegradation of photo-oxidized lignite and characterization of the products

NASA Astrophysics Data System (ADS)

Li, Jiantao; Liu, Xiangrong; Yue, Zilin; Zhang, Yaowen

2018-01-01

Biodegradation of photo-oxidized Inner Mongolia lignite by pseudomonas aeruginosa was studied and the degradation percentage reached 56.27%, while the corresponding degradation percentage of the strain degrading raw Inner Mongolia lignite is only 23.16%. The degradation products were characterized. Proximate and ultimate analyses show that the higher oxygen content increased by photo-oxidation pretreatment maybe promoted the degradation process. Ultraviolet spectroscopy (UV) analysis of the liquid product reveals that it contains unsaturated structures and aromatic rings are the main structure units. Gas chromatography-mass spectrometry (GC-MS) analysis indicates that the main components of the ethyl acetate extracts are low molecular weight organic compounds, such as ketones, acids, hydrocarbons, esters and alcohols. Infrared spectroscopy (IR) analysis of raw lignite, photo-oxidized lignite and residual lignite demonstrates that the absorption peaks of functional groups in residual lignite disappeared or weakened obviously. Scanning electron microscopy (SEM) analysis manifests that small holes appear in photo-oxidized lignite surface, which may be promote the degradation process and this is only from the physical morphology aspects, so it can be inferred from the tests and analyses results that the more important reason of the high degradation percentage is mostly that the photo-oxidation pretreatment changes the chemical structures of lignite.

Investigation of the electronic ground states for a reduced pyridine(diimine) uranium series: evidence for a ligand tetraanion stabilized by a uranium dimer.

PubMed

Anderson, Nickolas H; Odoh, Samuel O; Williams, Ursula J; Lewis, Andrew J; Wagner, Gregory L; Lezama Pacheco, Juan; Kozimor, Stosh A; Gagliardi, Laura; Schelter, Eric J; Bart, Suzanne C

2015-04-15

The electronic structures of a series of highly reduced uranium complexes bearing the redox-active pyridine(diimine) ligand, (Mes)PDI(Me) ((Mes)PDI(Me) = 2,6-(2,4,6-Me3-C6H2-N═CMe)2C5H3N) have been investigated. The complexes, ((Mes)PDI(Me))UI3(THF) (1), ((Mes)PDI(Me))UI2(THF)2 (2), [((Mes)PDI(Me))UI]2 (3), and [((Mes)PDI(Me))U(THF)]2 (4), were examined using electronic and X-ray absorption spectroscopies, magnetometry, and computational analyses. Taken together, these studies suggest that all members of the series contain uranium(IV) centers with 5f (2) configurations and reduced ligand frameworks, specifically [(Mes)PDI(Me)](•/-), [(Mes)PDI(Me)](2-), [(Mes)PDI(Me)](3-) and [(Mes)PDI(Me)](4-), respectively. In the cases of 2, 3, and 4 no unpaired spin density was found on the ligands, indicating a singlet diradical ligand in monomeric 2 and ligand electron spin-pairing through dimerization in 3 and 4. Interaction energies, representing enthalpies of dimerization, of -116.0 and -144.4 kcal mol(-1) were calculated using DFT for the monomers of 3 and 4, respectively, showing there is a large stabilization gained by dimerization through uranium-arene bonds. Highlighted in these studies is compound 4, bearing a previously unobserved pyridine(diimine) tetraanion, that was uniquely stabilized by backbonding between uranium cations and the η(5)-pyridyl ring.

Hydrology of area 46, Northern Great Plains and Rocky Mountain coal provinces, North Dakota

USGS Publications Warehouse

Croft, M.G.; Crosby, Orlo A.

1987-01-01

This report is one of a series that describes the hydrology of coal provinces nationwide. The Northern Great Plains and Rocky Mountain Coal Provinces are divided into 20 separate reporting areas which are numbered 43 to 62. This report provides general hydrologic information for Area 46 using a brief text with accompanying maps, charts, or graphs. This information may be used to describe the hydrology of the general area of any existing or proposed mine. Some of the more obvious hydrologic problems of coal development that will need to be addressed before development are disruption of aquifers and potential contamination of streams, aquifers, and the atmosphere.Area 46 is in northwestern North Dakota and is composed of parts or all of 14 hydrologic units based on surface-water drainage basins. The area is drained by the Missouri and Souris Rivers.Lignite-bearing rocks of late Paleocene age underlie nearly all of Area 46. The thickest and most continuous lignite beds occur in the Sentinel Butte and Tongue River Members of the Fort Union Formation. Alluvial deposits and a veneer of glacial drift of late Pleistocene age overlie the lignite-bearing rocks. The climate of the area is semiarid. Mean annual precipitation ranges from 13.9 to 17.8 inches. Mean annual temperatures range from 37.7°F at Bowbells to 40.9°F at Williston. Mean monthly temperatures at Williston range from 8.3°F to 70°F. The growing season is about 125 days.A fairly comprehensive data base for streamflow and water quality in streams is available for Area 46. Many of the small-stream monitoring sites have been operated during the last few years to provide a data base before coal development. With the exception of the Missouri River, which is controlled by several dams, both the quantity and quality of water varies greatly in all streams. A ground-water observation network for water levels and water quality has been established through county ground-water resource investigations and other ground-water studies and provides an adequate data base. Three activities within the U.S. Geological Survey identify and provide access to hydrologic data. These are the National Water-Data Exchange (NAWDEX), the National Water-Data Storage and Retrieval System (WATSTORE), and the Office of Water-Data Coordination (OWDC).

Degradation of Coal by the Fungi Polyporus versicolor and Poria monticola

PubMed Central

Cohen, Martin S.; Gabriele, Peter D.

1982-01-01

We report that two species of basidiomycete fungi (Polyporus versicolor and Poria monticola) grow in minimal liquid or solid medium when supplemented with crushed lignite coal. The fungi also grow directly on crushed lignite coal. The growth of both fungi was observed qualitatively as the production and extension of hyphae. No fungal growth occurred in minimal agar medium without coal. The fungi degraded solid lignite coal to a black liquid product which never appeared in cultures unless fungi and coal were present together. Apparently, lignite coal can serve as the principal substrate for the growth of the fungi. Infrared analyses of the liquid products of lignite degradation showed both similarities to and differences from the original lignite. Images PMID:16346060

Solubilization of Australian lignites by microorganisms

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

Catcheside, D.E.A.; Mallett, K.J.; Cox, R.E.

1988-01-01

Australia has substantial lignite deposits, particularly in the Latrobe Valley in Victoria where 4.10/sup 10/ tons are accessible with available technologies. The authors have investigated the susceptibility of these coal to solubilization by microorganisms, including species additional to those already identified as active on North American lignites. The data presented here show that acid oxidized lignites from the Latrobe Valley are solubilized by each of seven species of microorganisms previously found to be active on Leonardite and oxidized North American lignites. These are the wood rot fungi: Trametes versicolor, Poria placenta and Phanerochaete chrysosporium, the lignin degrading prokaryote Streptomyces viridosporusmore » and three fungi isolated from lignite in Mississippi: Candida ML-13, Cunninghamelia YML-1 and Penicillium waksmanii.« less

Geology and recognition criteria for sandstone uranium deposits in mixed fluvial-shallow marine sedimentary sequences, South Texas. Final report

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

Adams, S.S.; Smith, R.B.

1981-01-01

Uranium deposits in the South Texas Uranium Region are classical roll-type deposits that formed at the margin of tongues of altered sandstone by the encroachment of oxidizing, uraniferous solutions into reduced aquifers containing pyrite and, in a few cases, carbonaceous plant material. Many of the uranium deposits in South Texas are dissimilar from the roll fronts of the Wyoming basins. The host sands for many of the deposits contain essentially no carbonaceous plant material, only abundant disseminated pyrite. Many of the deposits do not occur at the margin of altered (ferric oxide-bearing) sandstone tongues but rather occur entirely within reduced,more » pyurite-bearing sandstone. The abundance of pyrite within the sands probably reflects the introduction of H/sub 2/S up along faults from hydrocarbon accumulations at depth. Such introductions before ore formation prepared the sands for roll-front development, whereas post-ore introductions produced re-reduction of portions of the altered tongue, leaving the deposit suspended in reduced sandstone. Evidence from three deposits suggests that ore formation was not accompanied by the introduction of significant amounts of H/sub 2/S.« less

Geochemical features of the ore-bearing medium in uranium deposits in the Khiagda ore field

NASA Astrophysics Data System (ADS)

Kochkin, B. T.; Solodov, I. N.; Ganina, N. I.; Rekun, M. L.; Tarasov, N. N.; Shugina, G. A.; Shulik, L. S.

2017-09-01

The Neogene uranium deposits of the Khiagda ore field (KOF) belong to the paleovalley variety of the hydrogene type and differ from other deposits of this genetic type in the geological and geochemical localization conditions. The contemporary hydrogeochemical setting and microbiological composition of ore-bearing medium are discussed. The redox potential of the medium (Eh is as low as-400 mV) is much lower than those established at other hydrogenic deposits, both ancient Late Mesozoic and young Late Alpine, studied with the same methods in Russia, Uzbekistan, and southern Kazakhstan. The pH of subsurface water (6.86-8.13) differs in significant fluctuations both between neighboring deposits and within individual ore lodes. Hydrogen-forming and denitrifying bacteria are predominant in microbiological populations, whereas sulfate-reducing bacteria are low-active. The consideration of these factors allowed us to describe the mechanism of uranium ore conservation as resulting from the development of the cryolithic zone, which isolates ore lodes from the effect of the external medium. Carbonated water supplied from the basement along fault zones also participates in the formation of the present-day hydrogeochemical setting. Based on the features of the ore-bearing medium, we propose a method of borehole in situ acid leaching to increase the efficiency of mining in the Khiagda ore field.

JV Task 98 - Controlling Mercury Emissions for Utilities Firing Lignites from North America

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

Steven Benson

2007-06-15

This project compiled and summarized the findings and conclusions of research, development, and demonstration projects on controlling mercury from lignite coals. A significant amount of work has been conducted since 1994 on mercury in lignite, mercury measurement in flue gases, sorbent, sorbent enhancement additives, oxidation agent development, and full-scale demonstration of mercury control technologies. This report is focused on providing the lignite industry with an understanding of mercury issues associated with the combustion of lignite, as well as providing vital information on the methods to control mercury emissions in coal-fired power plants.

URANIUM PRECIPITATION PROCESS

DOEpatents

Thunaes, A.; Brown, E.A.; Smith, H.W.; Simard, R.

1957-12-01

A method for the recovery of uranium from sulfuric acid solutions is described. In the present process, sulfuric acid is added to the uranium bearing solution to bring the pH to between 1 and 1.8, preferably to about 1.4, and aluminum metal is then used as a reducing agent to convert hexavalent uranium to the tetravalent state. As the reaction proceeds, the pH rises amd a selective precipitation of uranium occurs resulting in a high grade precipitate. This process is an improvement over the process using metallic iron, in that metallic aluminum reacts less readily than metallic iron with sulfuric acid, thus avoiding consumption of the reducing agent and a raising of the pH without accomplishing the desired reduction of the hexavalent uranium in the solution. Another disadvantage to the use of iron is that positive ferric ions will precipitate with negative phosphate and arsenate ions at the pH range employed.

PROCESS OF SEPARATING URANIUM FROM AQUEOUS SOLUTION BY SOLVENT EXTRACTION

DOEpatents

Warf, J.C.

1958-08-19

A process is described for separating uranium values from aqueous uranyl nitrate solutions. The process consists in contacting the uramium bearing solution with an organic solvent, tributyl phosphate, preferably diluted with a less viscous organic liquida whereby the uranyl nitrate is extracted into the organic solvent phase. The uranvl nitrate may be recovered from the solvent phase bv back extracting with an aqueous mediuin.

PROCESS FOR THE CONCENTRATION OF ORES CONTAINING GOLD AND URANIUM

DOEpatents

Gaudin, A.M.; Dasher, J.

1958-06-10

ABS>A process is described for concentrating certain low grade uranium and gold bearing ores, in which the gangue is mainly quartz. The production of the concentrate is accomplished by subjecting the crushed ore to a froth floatation process using a fatty acid as a collector in conjunction with a potassium amyl xanthate collector. Pine oil is used as the frothing agent.

Microbial screening test for lignite degradation. Quarterly progress report No. 2, April-June 1985

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

Yen, T.F.

1985-01-01

Fractionation of lignite was performed by means of: (1) benzene-methanol followed by aqueous alkaline extraction; and (2) benzene followed by methanol-alkaline extraction. The residue obtained by the latter fractionation was oxidized by means of cupric oxide and separated into methanol soluble fraction and methanol insoluble residue. Methanol-alkaline fraction was further divided into methylene chloride extractable portion and methylene chloride non-extractable portion. Fourier Transform Infrared Spectroscopy (FT-IR) was employed to characterize functional groups present in the raw lignite sample, benzene-methanol fraction, aqueous alkaline fraction, lignite residue, and benzene fraction. FT-IR was also used for the analysis of both methylene chloride extractablemore » and non-extracted portions. The following are some functional groups identified by the spectra of the fractions mentioned above: OH, amide, aromatic, CH, CO, C=C, CH/sub 2/, C-CH/sub 3/, SiCH/sub 3/, epoxide, and C-O-C. Both, raw lignite sample and aqueous alkaline fraction produced positive results for P. versicolor growth, whereas benzene-methanol fraction and lignite residue produced negative results. Acclimation of P. versicolor to lignite was accomplished up to 80% lignite and 20% neopeptone and maltose. 10 refs., 9 figs., 6 tabs.« less

Uranium in Surface Waters and Sediments Affected by Historical Mining in the Denver West 1:100,000 Quadrangle, Colorado

USGS Publications Warehouse

Zielinski, Robert A.; Otton, James K.; Schumann, R. Randall; Wirt, Laurie

2008-01-01

Geochemical sampling of 82 stream waters and 87 stream sediments within mountainous areas immediately west of Denver, Colorado, was conducted by the U.S. Geological Survey in October 1994. The primary purpose was to evaluate regionally the effects of geology and past mining on the concentration and distribution of uranium. The study area contains uranium- and thorium-rich bedrock, numerous noneconomic occurrences of uranium minerals, and several uranium deposits of variable size and production history. During the sampling period, local streams had low discharge and were more susceptible to uranium-bearing acid drainage originating from historical mines of base- and precious-metal sulfides. Results indicated that the spatial distribution of Precambrian granites and metamorphic rocks strongly influences the concentration of uranium in stream sediments. Within-stream transport increases the dispersion of uranium- and thorium rich mineral grains derived primarily from granitic source rocks. Dissolved uranium occurs predominantly as uranyl carbonate complexes, and concentrations ranged from less than 1 to 65 micrograms per liter. Most values were less than 5 micrograms per liter, which is less than the current drinking water standard of 30 micrograms per liter and much less than locally applied aquatic-life toxicity standards of several hundred micrograms per liter. In local streams that are affected by uranium-bearing acid mine drainage, dissolved uranium is moderated by dilution and sorptive uptake by stream sediments. Sorbents include mineral alteration products and chemical precipitates of iron- and aluminum-oxyhydroxides, which form where acid drainage enters streams and is neutralized. Suspended uranium is relatively abundant in some stream segments affected by nearby acid drainage, which likely represents mobilization of these chemical precipitates. The 234U/238U activity ratio of acid drainage (0.95-1.0) is distinct from that of local surface waters (more than 1.05), and this distinctive isotopic composition may be preserved in iron-oxyhydroxide precipitates of acid drainage origin. The study area includes a particularly large vein-type uranium deposit (Schwartzwalder mine) with past uranium production. Stream water and sediment collected downstream from the mine's surface operations have locally anomalous concentrations of uranium. Fine-grained sediments downstream from the mine contain rare minute particles (10-20 micrometers) of uraninite, which is unstable in a stream environment and thus probably of recent origin related to mining. Additional rare particles of very fine grained (less than 5 micrometer) barite likely entered the stream as discharge from settling ponds in which barite precipitation was formerly used to scavenge dissolved radium from mine effluent.

Biodegradation and bioconversion of coals by fungi. Quarterly progress report No. 1, October 1-December 31, 1985. [Candida sp. and T. versicolor

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

Ward, B.

1985-01-01

Following a month-long start-up period during which the principal investigator traveled to several sites of lignite outcrops to collect samples, efforts were begun to isolate new strains of coal-bioconverting fungal strains. Out of about thirty different organisms isolated from weathered samples of three different types of lignite, three isolates exhibited biosolubilization of the one lignite tested to date. These organisms have not yet been identified but they appear to be new strains of lignite-degrading fungi. We have observed that degree of biosolubilization varies among apparently similar samples of the same lignite. Weathered lignite is more readily solubilized than is previouslymore » unexposed lignite, but even tests on weathered coal have not been consistently repeatable. We have begun experiments designed to identify one or more factors of weathering which render coal more readily attacked by fungi. We hope to establish methods whereby consistently repeatable assays can be performed on bioconversion of coals. 2 refs., 1 fig., 1 tab.« less

A comparative study of nitrogen conversion during pyrolysis of coconut fiber, its corresponding biochar and their blends with lignite.

PubMed

Liu, Zhengang; Balasubramanian, Rajasekhar

2014-01-01

In the present study, the conversion of fuel-N to HCN and NH3 was investigated during rapid pyrolysis of raw biomass (coconut fiber), its corresponding biochar and their blends with lignite within a temperature range of 600-900°C. The results showed that the raw biomass and the biochar showed totally different nitrogen partitioning between NH3 and HCN. HCN was the dominant nitrogen pollutant from pyrolysis of raw biomass, while for the biochar pyrolysis the yield of NH3 was slightly higher than that of HCN. Synergistic interactions occurred within both raw biomass/lignite and biochar/lignite blends, especially for the biochar/lignite blend, and resulted in reduced yields of HCN and NH3, decreased the total nitrogen percentage retained in the char and promoted harmless N2 formation. These findings suggest that biochar/lignite co-firing for energy production may have the enhanced benefit of reduced emissions of nitrogen pollutants than raw biomass/lignite. Copyright © 2013 Elsevier Ltd. All rights reserved.

RECONNAISSANCE FOR URANIUM IN ASPHALT-BEARING ROCKS IN THE WESTERN UNITED STATES

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

Hail, W.J. Jr.

1957-01-01

An appraisal of asphait-bearing rocks as potential sources of uranium was made during 1953 and 1954 in 45 areas in Calif., Utah, Wyo., Mont., N. Mex., Tex., Okla., and Mo. A total of 202 samples from these areas was analyzed for uranium. The oldest rocks sampled are Ordovician in age, and the youngest are Recent. Although none of the deposits are of value at this time as a source of U, some of the deposits may constitute a low-grade U resource, but recovery of the U will depend upon the primary use of the asphalt. Significant amounts of U lnmore » the ash of oil extracted from these rocks were found in samples from 7 of the 45 areas examined. These areas are Chalome Creek, McKittrick, Edna, and Los Alamos Calif.; Vernal, Utah; Sulphur, Okla.; and Ellis, Mo. The average U content in the ash of the extracted oil of samples from these 7 areas ranges from 0.028 to 0.376%. All except the Chalone Creek area contain large estimated reserves of asphalt-bearing rock, ranging from 15 million to almost 2 billion tons. The average U content of samples from 13 additiomal areas ranges from 0.020 to 0.06B% in the ash of the extracted oil. Many of these areas contain very large reserves of asphalt-bearing rocks. It is believed that most of the asphalt deposits are oil residues, and that the U was introduced during or after the late stages of oil movement and loss of the lighter oil fractions. (auth)« less

Release behavior of uranium in uranium mill tailings under environmental conditions.

PubMed

Liu, Bo; Peng, Tongjiang; Sun, Hongjuan; Yue, Huanjuan

2017-05-01

Uranium contamination is observed in sedimentary geochemical environments, but the geochemical and mineralogical processes that control uranium release from sediment are not fully appreciated. Identification of how sediments and water influence the release and migration of uranium is critical to improve the prevention of uranium contamination in soil and groundwater. To understand the process of uranium release and migration from uranium mill tailings under water chemistry conditions, uranium mill tailing samples from northwest China were investigated with batch leaching experiments. Results showed that water played an important role in uranium release from the tailing minerals. The uranium release was clearly influenced by contact time, liquid-solid ratio, particle size, and pH under water chemistry conditions. Longer contact time, higher liquid content, and extreme pH were all not conducive to the stabilization of uranium and accelerated the uranium release from the tailing mineral to the solution. The values of pH were found to significantly influence the extent and mechanisms of uranium release from minerals to water. Uranium release was monitored by a number of interactive processes, including dissolution of uranium-bearing minerals, uranium desorption from mineral surfaces, and formation of aqueous uranium complexes. Considering the impact of contact time, liquid-solid ratio, particle size, and pH on uranium release from uranium mill tailings, reducing the water content, decreasing the porosity of tailing dumps and controlling the pH of tailings were the key factors for prevention and management of environmental pollution in areas near uranium mines. Copyright © 2017 Elsevier Ltd. All rights reserved.

First Report of Microfaunal Remains from Lignitic Sequences of Bhavnagar Lignite Mine (khadsaliya Formation), Gujarat, India: Implication to Depositional Environments and Age

NASA Astrophysics Data System (ADS)

Maurya, A. S.

2016-12-01

FIRST REPORT OF MICROFAUNAL REMAINS FROM LIGNITIC SEQUENCES OF BHAVNAGAR LIGNITE MINE (KHADSALIYA FORMATION), GUJARAT, INDIA: IMPLICATION TO DEPOSITIONAL ENVIRONMENTS AND AGEABHAYANAND SINGH MAURYA1*, SANJAY KUMAR VERMA1, PRAGYA PANDEY11Department of Earth Sciences, Indian Institute of Technology Roorkee, Roorkee Moderately preserved fish otoliths, fish vertebra, bivalves, pteropods, ostracods and foraminifereral remains were recovered from the grey to greenish-grey clays of Khadsaliya Formation, Bhavnagar Lignite Mine (western India) and quantitatively analyzed to understand the depositional environment. The bio-facies assemblage is diverse and dominated by fauna Fishes, Bivalve, Pteropods and with rare occurrences of Ostracoda and Foraminifera. Fish fauna includes otoliths represented by Ambassidarum, Apogonidarum, Percoideorum and Gobiidarum vastani, out of which Gobiidarum vastani is possibly representing Ypresian (early Eocene). The Globanomalina ovalis a smaller planktic foraminifer is known to be a very short ranged species corresponds to Planktic Foranimiferal Zone 5 to 6 (P5-P6) i.e late Thanetian to early Yepresian. Presence of both fresh water (Lepisosteus, Osteoglossidae), fresh water (Cypridopsis) ostracods and shallow marine fauna (Enchodus, Egertonia and Stephanodus) of fish vertebra; (Cardita) bivalve, , marine water (Globanomalina, Eggrella, Pyrulinoides) foraminifer suggests that Bhavnagar lignite mine have an assemblage of admixed fauna and rocks of Khaldsiya formation at Bhavnagar Lignite mine deposited under marine transgressive-regressive cycles. Some of the microfauna from Bhavnagar lignite mine show close affinities with microfaunal assemblages of the Vastan lignite mine of Gujarat, India which is stated to be of Ypresian (early Eocene).

Lithofacies control of lignite distribution and ground-water quality, Wilcox group (Eocene), east-central Texas

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

Ayers, W.B. Jr.; Lewis, A.H.

1984-04-01

Deep lignite resources (200-2000 ft; 61-610 m) were evaluated regionally using 1470 geophysical well logs to interpret lithofacies, lignite occurrence, and resistivity (water quality). The regional distribution of lithofacies indicates that in the region, the Wilcox Group is a fluvial-deltaic system. The primary fluvial system entered the Wilcox coastal plain west of Waco, Texas, trended southeast, and supplied a 75-mi (120-km) wide fluvial-deltaic system comparable in size to the Mississippi system. Lignites are most abundant in the Calvert Bluff Formation (upper Wilcox). Lower Calvert Bluff lignites are thickest and most extensive southwest of the Navasota River, whereas those of themore » upper Calvert Bluff are thickest northeast of the Brazos River. In the shallow subsurface, Calvert Bluff lignites are found in dip-elongate low-sand areas (flood plains) between channel-sand belts. Basinward, laterally continuous lignites coincide with high net sand areas comprise of distributary channel sands indicative of a delta-plain setting. The wilcox Group is a major aquifer. Maps of resistivity values show that Wilcox channel sands are conduits for ground-water flow. High values of formation resistivity (low total dissolved solids) exist in recharge areas at outcrop and around salt domes. Elongate trends of high resistivity values extend tens of miles basinward and coincide with axes of major sands. Resistivity values decrease basinward and the 20 ohm-m contour delineates the downdip limit of fresh water. Lithofacies and lignite occurrence maps are guides to exploration for deep lignite. Resistivity maps can be used to explore for ground-water resources.« less

Organic compounds in water extracts of coal: links to Balkan endemic nephropathy.

PubMed

Maharaj, S V M; Orem, W H; Tatu, C A; Lerch, H E; Szilagyi, D N

2014-02-01

The Pliocene lignite hypothesis is an environmental hypothesis that has been proposed to explain the etiology of Balkan endemic nephropathy (BEN). Aqueous leaching experiments were conducted on a variety of coal samples in order to simulate groundwater leaching of organic compounds, and to further test the role of the Pliocene lignite hypothesis in the etiology of BEN. Experiments were performed on lignite coal samples from endemic BEN areas in Romania and Serbia, and lignite and bituminous coals from nonendemic regions in Romania and the USA. Room temperature, hot water bath, and Soxhlet aqueous extraction experiments were conducted between 25 and 80 °C, and from 5 to 128 days in duration. A greater number of organic compounds and in higher concentrations were present in all three types of leaching experiments involving endemic area Pliocene lignite samples compared to all other coals examined. A BEN causing molecule or molecules may be among phenols, PAHs, benzenes, and/or lignin degradation compounds. The proposed transport pathway of the Pliocene lignite hypothesis for organic compound exposure from endemic area Pliocene lignite coals to well and spring drinking water, is likely. Aromatic compounds leached by groundwater from Pliocene lignite deposits in the vicinity of endemic BEN areas may play a role in the etiology of the disease. A better understanding of organic compounds leached by groundwater from Pliocene lignite deposits may potentially lead to the identification and implementation of effective strategies for the prevention of exposure to the causative agent(s) for BEN, and in turn, prevention of the disease.

Uranium in surface soils: an easy-and-quick assay combining X-ray diffraction and fluorescence qualitative data

NASA Astrophysics Data System (ADS)

Figueiredo, M. O.; Silva, T. P.; Batista, M. J.; Leote, J.; Ferreira, M. L.; Limpo, V.

2009-04-01

Portugal has been a uranium-producer since the beginning of the last century. The uranium-rich area of Alto Alentejo, East-central Portugal, was identified more than fifty years ago [1]. Almost all the uranium-bearing mineralization occurs in schistose rocks of the contact metamorphic aureole produced by intrusion of the Hercynian monzonitic granite of Alto Alentejo into the pre-Ordovitian schist-greywacke complex forming deposits of vein and dissemination type. The Nisa uranium-reservoir, situated at the sharp border of a large and arch shaped granite pluton, was identified in 1957 [2] but its exploitation was considered economically impracticable until recently. However, its existence and the accumulated detritus of these prospect efforts are a concern for local populations [3]. A study of the near-surface soils close to the Nisa reservoir was therefore undertaken to assess the uranium retention by adsorption on clay components under the form of uranyl ions, [UO2]2+ [4-6] and its eventual release into the aquifer groundwater. As an attempt to very quickly appraise the presence of uranium in as-collected near-surface sediment samples a combination of laboratory X-ray techniques was designed: X-ray diffraction (XRD) to identify the mineral phases and roughly estimate its relative proportion plus X-ray fluorescence spectrometry in wavelength dispersive mode (XRF-WDS) to ascertain the presence of uranium and tentatively evaluate its content by comparison with selected chemical components of the soil. A description of the experimental methodology adopted for the implemented easy-and-quick uranium assay is presented. Obtained results compare quite well to the data of certified time-consuming analytical tests of uranium in those soil samples. [1] L. Pilar (1966) Conditions of formation of Nisa uranium deposit (in Portuguese). Comunic. Serv. Geol. Portugal, tomo L, 50-85. [2] C. Gonçalves & J.V. Teixeira Lopes (1971) Uranium deposit of Nisa: geological aspects of its discovery and valorisation (in Portuguese). Internal Rept., JEN, 20 pp. [3] http://www.naturtejo.com [4] J.A. Davis et al. (2006) Processes affecting transport of uranium in a suboxic aquifer. Phys. Chem. of the Earth 31, 548-555. [5] Y. Arai et al. (2007) Spectroscopic evidence for uranium bearing precipitates in Vadose zone sediments at the Hanford 300-Area site. Environ. Sci. Technol. 41, 4633-4639. [6] A. Kremleva, S. Krüger & N. Rösch (2008) Density functional model studies of uranyl adsorption on (001) surfaces of kaolinite. Langmuir 24, 9515-9524.

Petrography and geochemistry of the San Miguel lignite, Jackson Group (Eocene), south Texas

USGS Publications Warehouse

Warwick, Peter D.; Crowley, Sharon S.; Ruppert, Leslie F.; Pontolillo, James

1996-01-01

The San Miguel lignite deposit (late Eocene, lower Jackson Group) of south Texas consists of four or more thin (generally < 1 m thick) lignite benches that are separated by claystone and mudstone partings. The partings are composed of altered volcanic air-fall ash that has been reworked by tidal or channel processes associated with a back-barrier depositional environment. The purpose of this study is to examine the relationship between the ash yield and the petrographic and geochemical characteristics of the San Miguel lignite as mined. Particular attention is given to 12 of the environmentally sensitive trace elements (As, Be, Cd, Cr, Co, Hg, Mn, Ni, Pb, Sb, Se, and U) that have been identified as possible hazardous air pollutants (HAPs) by the United States Clean Air Act Amendments of 1990. A total of 29 rock and lignite samples were collected and characterized by geochemical and petrographic methods. The major conclusions of the study are as follows: (1) The distribution of Mn is inversely related to the ash yield of the lignite samples. This indicates an organic affinity, or an association with finely disseminated minerals in the lignite that contain this element. (2) On a whole-coal basis, the concentration of the HAPs' element Pb is positively related to ash yield in lignite samples. This indicates an inorganic affinity for Pb. (3) Average whole-coal concentrations of As, Be, Sb, and U in the San Miguel samples are greater than published averages for these elements in other U.S. lignites. (4) The upper and lower lignite benches of the San Miguel deposit are both ash- and algal-rich, indicating that these intervals were probably deposited in wetter conditions than those in which the middle intervals formed. (5) The dominance of the eugelinite maceral subgroup over the huminite subgroup indicates that the San Miguel lignites were subjected to peat-forming conditions (either biogenic or chemical) that enabled degradation of wood cellular material into matrix gels, or that the plants that formed these lignite benches were less woody and more prone to formation of matrix gels. (6) An inertinite-rich layer (top of the B bed) might have formed from widespread oxidation of the San Miguel peat as a result of a volcanic ash fall which was subsequently reworked.

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

Nurten Vardar; Zehra Yumurtaci

The major gaseous emissions (e.g. sulfur dioxide, nitrogen oxides, carbon dioxide, and carbon monoxide), some various organic emissions (e.g. benzene, toluene and xylenes) and some trace metals (e.g. arsenic, cobalt, chromium, manganese and nickel) generated from lignite-fired power plants in Turkey are estimated. The estimations are made separately for each one of the thirteen plants that produced electricity in 2007, because the lignite-fired thermal plants in Turkey are installed near the regions where the lignite is mined, and characteristics and composition of lignite used in each power plant are quite different from a region to another. Emission factors methodology ismore » used for the estimations. The emission factors obtained from well-known literature are then modified depending on local moisture content of lignite. Emission rates and specific emissions (per MWh) of the pollutants from the plants without electrostatic precipitators and flue-gas desulfurization systems are found to be higher than emissions from the plants having electrostatic precipitators and flue -gas desulfurization systems. Finally a projection for the future emissions due to lignite-based power plants is given. Predicted demand for the increasing generation capacity based on the lignite-fired thermal power plant, from 2008 to 2017 is around 30%. 39 refs., 13 figs., 10 tabs.« less

Less-costly activated carbon for sewage treatment

NASA Technical Reports Server (NTRS)

Ingham, J. D.; Kalvinskas, J. J.; Mueller, W. A.

1977-01-01

Lignite-aided sewage treatment is based on absorption of dissolved pollutants by activated carbon. Settling sludge is removed and dried into cakes that are pyrolyzed with lignites to yield activated carbon. Lignite is less expensive than activated carbon previously used to supplement pyrolysis yield.

Physical exploration for uranium during 1951 in the Silver Reef district, Washington County, Utah

USGS Publications Warehouse

Stugard, Frederick

1954-01-01

During 1951 a joint exploration program of the most promising uraniferous areas in the Silver Reef district was made by the U.S. Geological Survey and the U.S. atomic Energy Commission. A U.S. Bureau of Mines drill crew, on contract to the Atomic Energy Commission, did 2,450 feet of diamond drilling under the geological supervision of the U.S. Geological Survey. The purpose of the drilling was to delineate broadly the favorable ground for commercial development of the uranium deposits. Ten drill holes were located around Pumpkin Point, which is the northeastern end of Buckeye Reef, to probe for extensions of small ore sheets mined on the Point in fine-grained sandstones of the Chinle formation. Three additional holes were located around Tecumseh Hill to probe for extensions of the small showings of uranium-bearing rocks of Buckeye Reef. Only one trace of uranium mineral was detected in the 13 drill holes by logging of drill cores, gamma-ray logging of the holes, and analysis of many core splits from favorable lithology. Extensive traversing with Geiger counters throughout the district and detailed geologic mapping of areas on Buckeye Reef and on East Reef indicate that the chances of discovering significant uranium deposits in the Silver Reef district are very poor, because of: highly variable lithology, closely faulted structure, and obliteration of the shallow uranium-bearing lenses by silver mining. Most of the available ore in the district was in the Pumpkin Point area and has been mined during 1950 to 1953. No ore reserves can be computed for the district before further development work. The most favorable remaining area in the district is now being explored by the operators with Atomic Energy Commission supervision.

Identification of Uranium Minerals in Natural U-Bearing Rocks Using Infrared Reflectance Spectroscopy.

PubMed

Beiswenger, Toya N; Gallagher, Neal B; Myers, Tanya L; Szecsody, James E; Tonkyn, Russell G; Su, Yin-Fong; Sweet, Lucas E; Lewallen, Tricia A; Johnson, Timothy J

2018-02-01

The identification of minerals, including uranium-bearing species, is often a labor-intensive process using X-ray diffraction (XRD), fluorescence, or other solid-phase or wet chemical techniques. While handheld XRD and fluorescence instruments can aid in field applications, handheld infrared (IR) reflectance spectrometers can now also be used in industrial or field environments, with rapid, nondestructive identification possible via analysis of the solid's reflectance spectrum providing information not found in other techniques. In this paper, we report the use of laboratory methods that measure the IR hemispherical reflectance of solids using an integrating sphere and have applied it to the identification of mineral mixtures (i.e., rocks), with widely varying percentages of uranium mineral content. We then apply classical least squares (CLS) and multivariate curve resolution (MCR) methods to better discriminate the minerals (along with two pure uranium chemicals U 3 O 8 and UO 2 ) against many common natural and anthropogenic background materials (e.g., silica sand, asphalt, calcite, K-feldspar) with good success. Ground truth as to mineral content was attained primarily by XRD. Identification is facile and specific, both for samples that are pure or are partially composed of uranium (e.g., boltwoodite, tyuyamunite, etc.) or non-uranium minerals. The characteristic IR bands generate unique (or class-specific) bands, typically arising from similar chemical moieties or functional groups in the minerals: uranyls, phosphates, silicates, etc. In some cases, the chemical groups that provide spectral discrimination in the longwave IR reflectance by generating upward-going (reststrahlen) bands can provide discrimination in the midwave and shortwave IR via downward-going absorption features, i.e., weaker overtone or combination bands arising from the same chemical moieties.

A comparison of thermal behaviors of raw biomass, pyrolytic biochar and their blends with lignite.

PubMed

Liu, Zhengang; Balasubramanian, Rajasekhar

2013-10-01

In this study, thermal characteristics of raw biomass, corresponding pyrolytic biochars and their blends with lignite were investigated. The results showed that pyrolytic biochars had better fuel qualities than their parent biomass. In comparison to raw biomass, the combustion of the biochars shifted towards higher temperature and occurred at continuous temperature zones. The biochar addition in lignite increased the reactivities of the blends. Obvious interactions were observed between biomass/biochar and lignite and resulted in increased total burnout, shortened combustion time and increased maximum weight loss rate, indicating increased combustion efficiencies than that of lignite combustion alone. Regarding ash-related problems, the tendency to form slagging and fouling increased, when pyrolytic biochars were co-combusted with coal. This present study demonstrated that the pyrolytic biochars were more suitable than raw biomass to be co-combusted with lignite for energy generation in existing coal-fired power plants. Copyright © 2013 Elsevier Ltd. All rights reserved.

Mössbauer study of Fe mineralogy with respect to rank, type and Colombian carboniferous zone

NASA Astrophysics Data System (ADS)

Caballero, F. Reyes; Martínez Ovalle, S. A.; Díaz Lagos, M.; Gómez, O. P.; Blandón, A.

2017-11-01

The transmission mode of Fe-57 Mössbauer spectroscopy was used to identify iron bearing minerals and establish relationships between and among these minerals and the ranks and types of various carboniferous zones in Colombia. Maceral and mineral compositions vary significantly among Colombian carboniferous zones. These variations determine some of the final characteristics and potential uses of coal, and therefore significantly contribute to defining coal quality. A comparison of spectroscopy results shows that the thermal maturity of the Colombian coals ranges from lignite to semianthracite. Similarities and differences exist with respect to conventional parameters. The coals of Córdoba and Cauca have higher sulfur contents > 2 % ash contents. Iron bearing minerals identified included pyrite, which was, found everywhere, and illite, ankerite, siderite, iron sulfates were found in particular areas. Coals from Valle del Cauca, Córdoba, Caldas and Santander are characterized by oxidation of pyrite and its transformation into ferrous or ferric sulfate.

Appraisal of Hydrologic Information Needed in Anticipation of Lignite Mining in Lauderdale County, Tennessee

USGS Publications Warehouse

Parks, William Scott

1981-01-01

Lignite in western Tennessee occurs as lenses or beds at various stratigraphic horizons in the Coastal Plain sediments of Late Cretaceous and Tertiary age. The occurrence of this lignite has been known for many decades, but not until the energy crisis was it considered an important energy resource. In recent years, several energy companies have conducted extensive exploration programs in western Tennessee, and tremendous reserves of lignite have been found. From available information, Lauderdale County was selected as one of the counties where strip-mining of lignite will most likely occur. Lignite in this county occurs in the Jackson and Cockfield Formations, undivided, of Tertiary age. The hydrology of the county is known only from regional studies and the collection of some site-specific data. Therefore, in anticipation of the future mining of lignite, a plan is needed for obtaining hydrologic and geologic information to adequately define the hydrologic system before mining begins and to monitor the effects of strip-mining once it is begun. For this planning effort, available hydrologic, geologic, land use, and associated data were located and compiled; a summary description of the surface and shallow subsurface hydrologic system was prepared: the need for additional baseline hydrologic information was outlined; and plans to monitor the effects of strip-mining were proposed. This planning approach, although limited to a county area, has transferability to other Coastal Plain areas under consideration for strip-mining of lignite.

Texas lignite mining: Groundwater and slope stability control in the nineties and beyond

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

Lawrence J.

As lignite mining in Texas approaches and exceeds depths of 200 feet below ground level, rising costs demand that innovative mining approaches be used in order to maintain the economic viability of lignite mining. Groundwater and slope stability problems multiply at these depths, resulting in increasing focus on how to control these costs. Dewatering costs are consistently rising for the lignite industry, as deeper mining encounters more and larger saturated sand bodies. These sands require dewatering in order to improve slope stability. Planning and analysis become more important as the number of wells grows beyond what can be managed withmore » a simple {open_quotes}cookie-cutter{close_quotes} approach. Slope stability plays an increasing role in mining concerns as deeper lignite is recovered. Slope stability causes several problems, including loss of lignite, increased rehandle, and hazards to personnel and equipment. Traditional lignite mine planning involved a fairly {open_quotes}generic{close_quotes} pit design with one design highwall angle, one design spoil angle, and little geotechnical evaluation of the deposit. This {open_quotes}one mine-one design{close_quotes} approach, while cost-effective in the past, is now being replaced by a more critical analysis of the design requirements of each area. Geotechnical evaluation plays an increasing role in the planning and operational aspects of lignite mining. Laboratory core sample test results can be used for slope stability modeling, in order to obtain more accurate design and operational information.« less

Preliminary notes on distribution of uranium in the Florida pebble phosphate field and suggestions for studying and sampling

USGS Publications Warehouse

,

1948-01-01

The accompanying map and sections show examples of the present state of information about the occurrence of the "Leached" uranium-bearing bed in the Florida pebble phosphate district. The dashed lines on the map define, as closely as present data permit, the limit of the area in which this bed contains significant amounts of uranium. The figures next to localities on the map indicate first, the thickness of the bed in feet; and second the uranium content in thousandths of percent. For example, the figures 16-10 next to the TVA localities in Secs. 9 and 10, T. 32 S., R. 26 E. indicate 16 feet at 0.010 percent uranium. A "0" by a locality indicates either that the uranium content is less than 0.001 percent or less than the concentration in the underlying phosphate beds (matrix of the miners) or that the leached bed is not present.

Selected annotated bibliography of the geology and occurrence of uranium-bearing marine black shales in the United States

USGS Publications Warehouse

Fix, Carolyn E.

1956-01-01

The bibliography consists of annotations or abstracts of selected reports that pertain to the geology and occurrence of uranium in marine black shales and their metamorphic equivalents in the United States. Only those reports that were available to the public prior to June 30, 1956, are included. Most of the reports may be consulted in the larger public, university, or scientific libraries. A few reports that have been released to the public in open file may be consulted at designated offices of the Geological Survey. An effort has been made to include only those references to shales whose uranium is believed to be of syngenetic origin and whose major source of radioactivity is uranium. Many general papers on the geology of uranium deposits refer to marine black shales, and some of these general papers have been included.

Botanical prospecting for uranium on La Ventana Mesa, Sandoval County, New Mexico

USGS Publications Warehouse

Starrett, Wm. H.; Cannon, Helen L.

1954-01-01

A botanical sampling program has been completed by the U.S. Geological Survey on La Ventana Mesa, Sandoval County, N. Mex. A uranium-bearing coal in the Allison-Gibson members of the Cretaceous Mesaverde formation crops out in erosional remnants of the mesa.The coal is capped by a well-fractured 65-foot sandstone bed through which roots of a pinyon-juniper forest penetrate. Samples of several hundred branches of trees growing on top of the mesa were collected and analyzed for uranium. The assays ranged from 0.1 part per million to 2.3 ppm uranium in the wood ash. Dead branches, which were found to contain more uranium in the ash than live branches, were sampled where possible. The results have been contoured to indicated probable areas of mineralized coal. Parts of the north butte are recommended as favorable for physical exploration.

METHOD OF MAKING WIRE FUEL ELEMENTS

DOEpatents

Zambrow, J.L.

1960-08-01

A method is given for making a nuclear reactor fuel element in the form of a uranium-bearing wire clad with zirconium. A uranium bar is enclosed in a zirconium sheath which is coated with an oxide of magnesium, beryllium, or zirconium. The sheathed bar is then placed in a steel tube and reduced to the desired diameter by swaging at 800 to 900 deg C, after which the steel and oxide are removed.

Uranium hydrogeochemical and stream sediment reconnaissance of the Newcastle NTMS quadrangle, Wyoming, including concentrations of forty-two additional elements

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

Goff, S.J.; Sandoval, W.F.; Gallimore, D.L.

1980-06-01

During the summer and fall of 1977, 533 water and 1226 sediment samples were collected from 1740 locations within the 18,000 km/sup 2/ area of the Newcastle quadrangle, Wyoming. Water samples were collected from wells and springs; sediment samples were collected from stream channels and from springs. Each water sample was analyzed for uranium, and each sediment sample was analyzed for 43 elements, including uranium and thorium. Uranium concentrations in water samples range from below the detection limit of 0.02 ppB to 702.26 ppB and have a median of 1.73 ppB and a mean of 11.76 ppB. Water samples containingmore » high uranium concentrations (>20 ppB) generally are associated with known uranium mining activity or units known to be uranium bearing. About one-third of the water samples containing high uranium concentrations were collected from locations within the Pumpkin Buttes and Turnercrest-Ross Districts. Nearly half of the water samples containing high uranium concentrations were collected from locations just west of the Monument Hill and Highland Flats-Box Creek Districts. Similar anomalous uranium concentrations in this region have been reported updip from Exxon's Highland uranium deposits. High uranium concentrations were also found associated with the Lance Creek-Old Woman Anticline District.« less

Preliminary summary review of thorium-bearing mineral occurrences in Alaska

USGS Publications Warehouse

Bates, Robert G.; Wedow, Helmuth

1952-01-01

Thorium-bearing minerals are known at 47 localities in Alaska. At these localities the thorium occurs as a major constituent or in minor amounts as an impurity in one or more of the following 12 minerals: allanite, columbite, ellsworthite, eschynite, gummite, monazite, orangite, parisite, thorianite, thorite, xenotime, and zircon. In addition other minerals, such as biotite and sphene, are radioactive and may contain thorium. Several unidentified columbate minerals with uranium or thorium and uranium as major constituents have been recognized at some localities. The distribution, by type of deposit, of the 57 thorium occurrences is as follows: lode - 3, lode and placer - 1, granitic rock - 3, granitic rock and related placer - 14, and placer - 26. Of the four lode occurrences only the radioactive veins at Salmon Bay in southeastern Alaska and the contact metamorphic deposit in the Nixon Fork area of central Alaska warrant further consideration, although insufficient data are available to determine whether these two deposits have commercial possibilities. The remaining occurrences of thorium-bearing minerals in Alaska are limited to placer deposits and disseminations of accessory minerals in granitic rocks. In most of these occurrences the thorium-bearing minerals occur in only trace amounts and consequently warrent little further consideration. More data are needed to determine the possibilities of byproduct recovery of thorium-bearing minerals from several of the gold and tin placers.

Geology and preliminary dating of the hominid-bearing sedimentary fill of the Sima de los Huesos Chamber, Cueva Mayor of the Sierra de Atapuerca, Burgos, Spain.

PubMed

Bischoff, J L; Fitzpatrick, J A; León, L; Arsuagà, J L; Falgueres, C; Bahain, J J; Bullen, T

1997-01-01

Sediments of the Sima de los Huesos vary greatly over distances of a few meters. This is typical of interior cave facies, and caused by cycles of cut and fill. Mud breccias containing human bones, grading upwards to mud containing bear bones, fill an irregular surface cut into basal marks and sands. The lack of Bedding and the chaotic abundance of fragile speleothem clasts in the fossiliferous muds suggests that the deposit was originally a subterranean pond facies, and that after emplacement of the human remains, underwent vigorous post-depositional rotation and collapse and brecciation, caused by underlying bedrock dissolution and undermining. The fossiliferous deposits are capped by flowstone and guano-bearing muds which lack large-mammal fossils. U-series and radiocarbon dating indicates the capping flowstones formed from about 68 ka to about 25 ka. U-series analyses of speleothem clasts among the human fossils indicate that all are at, or close to, isotopic equilibrium (> 350 ka). The distribution of U-series dates for 25 bear bones (154 +/- 66 ka) and for 16 human bones (148 +/- 34 ka) is similar and rather broad. Because the human bones seem to be stratigraphically older than chose of the bears, the results would indicate that most of the bones have been accumulating uranium irregularly with time. Electron spin resonance (ESR) analyses of six selected bear bones indicates dates of 189 +/- 28 ka, for which each is cordant with their corresponding U-series date (181 +/- 41 ka). Combined ESR and U-series dates for these samples yielded 200 +/- 4 ka. Such agreement is highly suggestive that uranium uptake in these bones was close to the early-uptake (EU) model, and the dates are essentially correct. Another three selected samples yielded combined ESR U-series dates of 320 +/- 4 ka with a modeled intermediate-mode of uranium uptake. The dating results, therefore, seem to provide a firm minimum age of about 200 ka for the human entry: and suggestive evidence of entry before 320 ka.

Geology and preliminary dating of the hominid-bearing sedimentary fill of the Sima de los Huesos Chamber, Cueva Mayor of the Sierra de Atapuerca, Burgos, Spain

USGS Publications Warehouse

Bischoff, J.L.; Fitzpatrick, J.A.; Leon, L.; Arsuaga, J.L.; Falgueres, Christophe; Bahain, J.-J.; Bullen, T.

1997-01-01

Sediments of the Sima de los Huesos vary greatly over distances of a few meters. This is typical of interior cave facies, and caused by cycles of cut and fill. Mud breccias containing human bones, grading upwards to mud containing bear bones, fill an irregular surface cut into basal marls and sands. The lack of bedding and the chaotic abundance of fragile speleothem clasts in the fossiliferous muds suggests that the deposit was originally a subterranean pond facies, and that after emplacement of the human remains, underwent vigorous post-depositional rotation and collapse and brecciation, caused by underlying bedrock dissolution and undermining. The fossiliferous deposits are capped by flowstone and guano-bearing muds which lack large-mammal fossils. U-series and radiocarbon dating indicates the capping flowstones formed from about 68 ka to about 25 ka. U-series analyses of speleothem clasts among the human fossils indicate that all are at, or close to, isotopic equilibrium (>350 ka). The distribution of U-series dates for 25 bear bones (154??66ka) and for 16 human bones (148??34 ka) is similar and rather broad. Because the human bones seem to be stratigraphically older than those of the bears, the results would indicate that most of the bones have been accumulating uranium irregularly with time. Electron spin resonance (ESR) analyses of six selected bear bones indicates dates of 189??28 ka, for which each is concordant with their corresponding U-series date (181??41 ka). Combined ESR and U-series dates for these samples yielded 200??4 ka. Such agreement is highly suggestive that uranium uptake in these bones was close to the early-uptake (EU) model, and the dates are essentially correct. Another three selected samples yielded combined ESR-U-series dates of 320??4 ka with a modeled intermediate-mode of uranium uptake. The dating results, therefore, seem to provide a firm minimum age of about 200 ka for the human entry; and suggestive evidence of entry before 320 ka. ?? 1997 Academic Press Limited.

Preliminary report on near-surface lignite occurrences, Cleveland County, Arkansas

USGS Publications Warehouse

Heermann, Stephen E.

1983-01-01

Four cross sections were constructed from lithologic descriptions of 43 drill holes in Cleveland County, Ark., in order to illustrate the occurrence of lignite and to relate the lignite beds to the regional stratigraphic framework. Of 43 holes drilled, 8 contained beds of lignite, but only two had beds greater than 30 in. thick. These beds are apparently lenticular and are restricted to the upper 60 ft. of the Cockfield Formation of the Claiborne Group of Middle Eocene age. The Cockfield Formation is at or near the surface west of the Saline River.

Liquefaction/solubilization of low-rank Turkish coals by white-rot fungus (Phanerochaete chrysosporium)

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

Elbeyli, I.Y.; Palantoken, A.; Piskin, S.

2006-08-15

Microbial coal liquefaction/solubilization of three low-rank Turkish coals (Bursa-Kestelek, Kutahya-Seyitomer and Mugla-Yatagan lignite) was attempted by using a white-rot fungus (Phanerochaete chrysosporium DSM No. 6909); chemical compositions of the products were investigated. The lignite samples were oxidized by nitric acid under moderate conditions and then oxidized samples were placed on the agar medium of Phanerochaete chrysosporium. FTIR spectra of raw lignites, oxidized lignites and liquid products were recorded, and the acetone-soluble fractions of these samples were identified by GC-MS technique. Results show that the fungus affects the nitro and carboxyl/carbonyl groups in oxidized lignite sample, the liquid products obtained bymore » microbial effects are the mixture of water-soluble compounds, and show limited organic solubility.« less

Canned pump having a high inertia flywheel

DOEpatents

Veronesi, Luciano; Raimondi, ALbert A.

1989-01-01

A canned pump is described which includes a motor, impeller, shaft, and high inertia flywheel mounted within a hermetically sealed casing. The flywheel comprises a heavy metal disk made preferably of a uranium alloy with a stainless steel shell sealably enclosing the heavy metal. The outside surfaces of the stainless steel comprise thrust runners and a journal for mating with, respectively, thrust bearing shoes and radial bearing segments. The bearings prevent vibration of the pump and, simultaneously, minimize power losses normally associated with the flywheel resulting from frictionally pumping surrounding fluid.

Canned pump having a high inertia flywheel

DOEpatents

Veronesi, L.; Raimondi, A.A.

1989-12-12

A canned pump is described which includes a motor, impeller, shaft, and high inertia flywheel mounted within a hermetically sealed casing. The flywheel comprises a heavy metal disk made preferably of a uranium alloy with a stainless steel shell sealably enclosing the heavy metal. The outside surfaces of the stainless steel comprise thrust runners and a journal for mating with, respectively, thrust bearing shoes and radial bearing segments. The bearings prevent vibration of the pump and, simultaneously, minimize power losses normally associated with the flywheel resulting from frictionally pumping surrounding fluid. 5 figs.

Uniform deposition of uranium hexafluoride (UF6): Standardized mass deposits and controlled isotopic ratios using a thermal fluorination method

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

McNamara, Bruce K.; O’Hara, Matthew J.; Casella, Andrew M.

2016-07-01

Abstract: We report a convenient method for the generation of volatile uranium hexafluoride (UF6) from solid uranium oxides and other uranium compounds, followed by uniform deposition of low levels of UF6 onto sampling coupons. Under laminar flow conditions, UF6 is shown to interact with surfaces within the chamber to a highly predictable degree. We demonstrate the preparation of uranium deposits that range between ~0.01 and 470±34 ng∙cm-2. The data suggest the method can be extended to creating depositions at the sub-picogram∙cm-2 level. Additionally, the isotopic composition of the deposits can be customized by selection of the uranium source materials. Wemore » demonstrate a layering technique whereby two uranium solids, each with a different isotopic composition, are employed to form successive layers of UF6 on a surface. The result is an ultra-thin deposit of UF6 that bears an isotopic signature that is a composite of the two uranium sources. The reported deposition method has direct application to the development of unique analytical standards for nuclear safeguards and forensics.« less

Regularities of spatial association of major endogenous uranium deposits and kimberlitic dykes in the uranium ore regions of the Ukrainian Shield

NASA Astrophysics Data System (ADS)

Kalashnyk, Anna

2015-04-01

During exploration works we discovered the spatial association and proximity time formation of kimberlite dykes (ages are 1,815 and 1,900 Ga for phlogopite) and major industrial uranium deposits in carbonate-sodium metasomatites (age of the main uranium ore of an albititic formation is 1,85-1,70 Ga according to U-Pb method) in Kirovogradsky, Krivorozhsky and Alekseevsko-Lysogorskiy uranium ore regions of the Ukrainian Shield (UkrSh) [1]. In kimberlites of Kirovogradsky ore region uranium content reaches 18-20 g/t. Carbon dioxide is a major component in the formation of hydrothermal uranium deposits and the formation of the sodium in the process of generating the spectrum of alkaline ultrabasic magmas in the range from picritic to kimberlite and this is the connection between these disparate geochemical processes. For industrial uranium deposits in carbonate-sodium metasomatitics of the Kirovogradsky and Krivorozhsky uranium ore regions are characteristic of uranyl carbonate introduction of uranium, which causes correlation between CO2 content and U in range of "poor - ordinary - rich" uranium ore. In productive areas of uranium-ore fields of the Kirovogradsky ore region for phlogopite-carbonate veinlets of uranium ore albitites deep δ13C values (from -7.9 to -6.9o/oo) are characteristic. Isotope-geochemical investigation of albitites from Novokonstantynovskoe, Dokuchaevskoe, Partyzanskoe uranium deposits allowed obtaining direct evidence of the involvement of mantle material during formation of uranium albitites in Kirovogradsky ore region [2]. Petrological characteristics of kimberlites from uranium ore regions of the UkrSh (presence of nodules of dunite and harzburgite garnet in kimberlites, diamonds of peridotite paragenesis, chemical composition of indicator minerals of kimberlite, in particular Gruzskoy areas pyropes (Cr2O3 = 6,1-7,1%, MgO = 19,33-20,01%, CaO = 4,14-4,38 %, the content of knorringite component of most grains > 50mol%), chromites (Cr2O3 = 45,32-62,17%, MgO = 7,3-12,5%) allow us to estimate the depth of generation of kimberlite magmas more than 170-200 km. Ilmenites show two groups according to MgO, Cr2O3 and TiO2 content. Reconstructions of the mantle sections show also two intervals of pressures divided at 4.5 GPa, the upper part is highly metasomatized This high degree metasomatism is determined for almost all mantle columns. It is suggested that large-scale of uranium-bearing mantle fluids may be associated with the ancient degasation during the subduction which is highly enriched in U component . Analysis of the reasons for the marked association kimberlitic dykes and major industrial uranium deposits in carbonate-sodium metasomatic in the UkrSh led to the conclusion that hydrothermal uranium deposits are confined to the supply mantle fluid systems of mantle fault zones exercising brings sodium carbonate solutions enriched uranium from mantle sources. References: 1. Kalashnik A.A. New prognostic-evaluation criteria in technology prognosis of forming industrial endogenous uranium deposits of the Ukrainian Shield, 2014. Scientific proceedings of UkrSGRI, № 2, p. 27-54 (in Russian) 2. Stepanjuk L.M., Bondarenko S.V., Somka V.O. and other, 2012. Source of uranium and uranium-bearing sodium albitites for example of Dokuchaievskogo field of the Ingulsky megablock of the UkrSh: Abstracts of scientific conference "Theoretical issues and research practice metasomatic rocks and ores" (Kyiv, 14-16 March 2012), IGMOF, p.78-80. (in Ukrainian)

Comparison of artificial maturation of lignite in hydrous and nonhydrous conditions

USGS Publications Warehouse

Behar, F.; Lewan, M.D.; Lorant, F.; Vandenbroucke, M.

2003-01-01

The objectives of the study are to compare product compositions and yields generated from lignite artificially matured by open nonhydrous pyrolysis, closed nonhydrous pyrolysis, and hydrous pyrolysis. The pyrolysis products were fractionated into CO2, H2O, CH4, C2-C5, C8-C14, C14+ saturates, C14+ aromatics and NSOs (resins+asphaltenes). All three methods generated high and similar quantities of water during pyrolysis that ranged between 14.6 and 15.2 wt.% of the original lignite. As a result of this high water content generated by the lignite, the experiments with no added water are referred to as nonhydrous rather than anhydrous. Rock-Eval pyrolysis and elemental analyses were conducted on the recovered lignite after solvent extraction to determine their residual hydrocarbon generation potential and to plot their position in a van Krevelen diagram, respectively. Residual lignite from the closed nonhydrous and hydrous experiments showed relationships between vitrinite reflectance (%Ro) values and atomic H/C ratios that occurred within the fields observed for natural maturation of coal. Although no significant differences in the atomic H/C ratios were observed between closed nonhydrous and hydrous pyrolysis, the vitrinite reflectance values were on the average 0.2% Ro lower in the residual lignite from the nonhydrous experiments. The remaining hydrocarbon generation potential as determined by Rock-Eval pyrolysis of the residual lignite showed that the nonhydrous residuals had on the average 16 mg more hydrocarbon potential per gram of original lignite than the hydrous residuals. This suggests there is a better release of the pyrolysis products from the lignite network in the hydrous experiments once generation occurs. For gas generation, at maximum yields, open nonhydrous pyrolysis generates the most hydrocarbon gas (21.0 mg/g original lignite), which is 20% more than closed nonhydrous pyrolysis and 29% more than hydrous pyrolysis. Closed nonhydrous pyrolysis generates on the average 14% more gas than hydrous pyrolysis, but the proportionality of the generated hydrocarbon gases is essentially the same for both pyrolysis methods. At maximum yields, CO2 generation is greatest in hydrous pyrolysis (99.5 mg/g original lignite), with yields being 37 percent higher than closed nonhydrous pyrolysis and 26% higher than open nonhydrous pyrolysis. The maximum yields of C14+ products are highest and similar for open nonhydrous pyrolysis and hydrous pyrolysis (125.6 and 125.9 mg/g lignite, respectively), and are more than 70% higher than closed nonhydrous pyrolysis. This difference in the maximum yields of C14+ products can be explained by differences in the proportionality between either cracking reactions that result in liquid product and char formation or trapping of generated products within the coal network (cross-linking reactions). Maximum yields of C14+ aliphatics from hydrous experiments may not have been attained, but the maximums that were observed and their GC traces are similar for the three pyrolysis systems.

PROCESS OF SEPARATING PLUTONIUM FROM URANIUM

DOEpatents

Brown, H.S.; Hill, O.F.

1958-09-01

A process is presented for recovering plutonium values from aqueous solutions. It comprises forming a uranous hydroxide precipitate in such a plutonium bearing solution, at a pH of at least 5. The plutonium values are precipitated with and carried by the uranium hydroxide. The carrier precipitate is then redissolved in acid solution and the pH is adjusted to about 2.5, causing precipitation of the uranous hydroxide but leaving the still soluble plutonium values in solution.

Effects of lignite application on ammonia and nitrous oxide emissions from cattle pens.

PubMed

Sun, Jianlei; Bai, Mei; Shen, Jianlin; Griffith, David W T; Denmead, Owen T; Hill, Julian; Lam, Shu Kee; Mosier, Arvin R; Chen, Deli

2016-09-15

Beef cattle feedlots are a major source of ammonia (NH3) emissions from livestock industries. We investigated the effects of lignite surface applications on NH3 and nitrous oxide (N2O) emissions from beef cattle feedlot pens. Two rates of lignite, 3 and 6kgm(-2), were tested in the treatment pen. No lignite was applied in the control pen. Twenty-four Black Angus steers were fed identical commercial rations in each pen. We measured NH3 and N2O concentrations continuously from 4th Sep to 13th Nov 2014 using Quantum Cascade Laser (QCL) NH3 analysers and a closed-path Fourier Transform Infrared Spectroscopy analyser (CP-FTIR) in conjunction with the integrated horizontal flux method to calculate NH3 and N2O fluxes. During the feeding period, 16 and 26% of the excreted nitrogen (N) (240gNhead(-1)day(-1)) was lost via NH3 volatilization from the control pen, while lignite application decreased NH3 volatilization to 12 and 18% of the excreted N, for Phase 1 and Phase 2, respectively. Compared to the control pen, lignite application decreased NH3 emissions by approximately 30%. Nitrous oxide emissions from the cattle pens were small, 0.10 and 0.14gN2O-Nhead(-1)day(-1) (<0.1% of excreted N) for the control pen, for Phase 1 and Phase 2, respectively. Lignite application increased direct N2O emissions by 40 and 57%, to 0.14 and 0.22gN2O-Nhead(-1)day(-1), for Phase 1 and Phase 2, respectively. The increase in N2O emissions resulting from lignite application was counteracted by the lower indirect N2O emission due to decreased NH3 volatilization. Using 1% as a default emission factor of deposited NH3 for indirect N2O emissions, the application of lignite decreased total N2O emissions. Copyright © 2016 Elsevier B.V. All rights reserved.

78 FR 63463 - Intent To Prepare a Regional Environmental Impact Statement for Surface Coal and Lignite Mining...

Federal Register 2010, 2011, 2012, 2013, 2014

2013-10-24

... Environmental Impact Statement for Surface Coal and Lignite Mining in the State of Texas AGENCY: Department of..., indirect, and cumulative effects associated with a decision to develop and assess data and information with... responsibility. These coal and lignite mining activities may eventually require authorization from the USACE...

The mineral base and productive capacities of metals and non-metals of Kosovo

NASA Astrophysics Data System (ADS)

Rizaj, M.; Beqiri, E.; McBow, I.; O'Brien, E. Z.; Kongoli, F.

2008-08-01

All historical periods of Kosovo—Ilirik, Roman, Medieval, Turkish, and former Yugoslavian—are linked with the intensive development of mining and metallurgy. This activity influenced and still is influencing the overall position of Kosovo as a country. For example, according to a 2006 World Bank report as well as other studies, Kosovo has potential lignite resources (geological reserves) of about 1.5 billion tonnes, which are ranked fifth in the world in importance. Other significant Kosovan mineral resources include lead, zinc, gold, silver, bauxite, and uranium, and rare metals accompanying those minerals, including indium, cadmium, thallium, gallium, and bismuth. These rare metals are of particular importance in developing advanced industrial technologies. Kosovo also has reserves of high-quality non-metals, including magnesite, quartz grit, bentonite, argil, talc, and asbestos. No database exists for these non-metal reserves, and further research and studies are needed.

The mineral base and productive capacities of metals and non-metals of Kosovo

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

Rizaj, M.; Beqiri, E.; McBow, I.

2008-08-15

All historical periods of Kosovo - Ilirik, Roman, Medieval, Turkish, and former Yugoslavian - are linked with the intensive development of mining and metallurgy. This activity influenced and still is influencing the overall position of Kosovo as a country. For example, according to a 2006 World Bank report as well as other studies, Kosovo has potential lignite resources (geological reserves) of about 1.5 billion tonnes, which are ranked fifth in the world in importance. Other significant Kosovan mineral resources include lead, zinc, gold, silver, bauxite, and uranium, and rare metals accompanying those minerals, including indium, cadmium, thallium, gallium, and bismuth.more » These rare metals are of particular importance in developing advanced industrial technologies. Kosovo also has reserves of high-quality non-metals, including magnesite, quartz grit, bentonite, argil, talc, and asbestos. No database exists for these non-metal reserves, and further research and studies are needed.« less

METHOD OF DISSOLVING REFRACTORY ALLOYS

DOEpatents

Helton, D.M.; Savolainen, J.K.

1963-04-23

This patent relates to the dissolution of alloys of uranium with zirconium, thorium, molybdenum, or niobium. The alloy is contacted with an anhydrous solution of mercuric chloride in a low-molecular-weight monohydric alcohol to produce a mercury-containing alcohol slurry. The slurry is then converted to an aqueous system by adding water and driving off the alcohol. The resulting aqueous slurry is electrolyzed in the presence of a mercury cathode to remove the mercury and produce a uranium-bearing aqueous solution. This process is useful for dissolving irradiated nuclear reactor fuels for radiochemical reprocessing by solvent extraction. In addition, zirconium-alloy cladding is selectively removed from uranium dioxide fuel compacts by this means. (AEC)

Selective uptake of uranium and thorium by some vegetables

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

Yusof, A.M.; Ghazali, Z.; Rahman, S.A.

1996-12-31

Uranium and thorium are trace elements in the actinide series found naturally in the atmosphere and can enter the human body through ingestion of food or by drinking. To establish baseline information for current and future environmental assessment due to pollution, especially in foodstuff, by heavy and trace metals, biological samples such as locally grown vegetables were analyzed for uranium and thorium contents. The terrain in most parts of the Malaysian peninsula consists of monazite-bearing rocks or soil that can be found extensively in areas related to tin-mining operations. Abandoned mining areas provide suitable sites for vegetable cultivation where mostmore » vegetables in the lowlands are grown.« less

Water resources of the Rattlesnake Butte area, a site of potential lignite mining in west-central North Dakota

USGS Publications Warehouse

Horak, W.F.

1983-01-01

In much of western North Dakota, minable lignite beds and associated sand beds are valuable local aquifers. Strip mining disrupts the aquifers and could significantly impact the local hydrology, imposing hardships on local residents. This comprehensive water-resources study of a 147-square-mile coal area in west-central North Dakota was done to facilitate sound management decisions regarding the suitability of the site for mining. Two strippable lignite beds, identified as the D and E beds, in the lower 250 to 300 feet of the Sentinel Butte Member of the Fort Union Formation underlie much of two small stream basins. The lignites and two closely associated sand deposits are the only consistently occurring aquifers within several hundred feet of the land surface. The D lignite bed underlies nearly the entire study area, but is not water bearing where it is structurally uplifted beneath upland areas. It is, for the most part, marginally confined. The E lignite bed overlies the D bed and is extensively eroded along North Creek in the southern part of the study area. The E bed is either unsaturated or unconfined in most of its area of occurrence. Direction of ground-water flow in both lignite aquifers is largely controlled by topography. Interconnected sand beds deposited as channel fill in braided streams form aquifers between the E and D beds (E-D aquifer) and below the D bed (D-HT aquifer). Both aquifers underlie the central part of the study area and each consists of as much as 100 feet of predominantly fine to medium silty unconsolidated sand. Maximum depth to the top of the aquifers was 200 feet for the E-D aquifer and 320 feet for the D-HT aquifer. The E-D aquifer, where near land surface, is unconfined, whereas the D-HT aquifer is entirely confined. Direction of ground-water flow in the D-HT aquifer is not influenced by the local topography as in the three overlying aquifers.Aquifers also occur at much greater depth beneath the study area in strata of Late Cretaceous and early Tertiary age. The Fox Hills and Tongue River aquifers are most commonly utilized and lie at depths of about 1,700 and 750 feet, respectively. Water in all aquifers beneath the study area is a sodium bicarbonate or sodium sulfate type. Mean dissolved solids in the four aquifers in the Sentinel Butte Member ranged from 1,290 to 1,970 milligrams per liter- Most of the samples were soft water, had low dissolved iron concentration, and were slightly to moderately colored (tan to brown) by dissolved organics. Several samples from the four aquifers had a perceptible hydrogen sulfide odor.North Creek and an unnamed tributary of the Green River drain most of the study area. North Creek flows intermittently during most years, while the Green River tributary flows perennially and has base flow of about 0.2 cubic foot per second. North Creek has predominately a sodium sulfate type water and the Green River tributary has a sodium bicarbonate-sulfate type water. At high flows, the dissolved solids generally are less than 1,000 milligrams per liter, and the water contains greater percentages of calcium and magnesium than at low flow.The impacts of strip mining on the shallow ground-water flow system would be very localized due to the already low water levels and the segmented nature of the flow system. Similarly, water-quality impacts on the ground-water system would be localized. Natural geochemical processes are effective in limiting the severity and lateral spread of chemically enriched waters. Streamflow magnitudes should not be significantly affected by mining activities. Stream quality impacts should be readily manageable by ordinary routing, impoundment, and treatment techniques.

Wall-rock control of cortain pitchblende deposits in Golden Gate Canyon, Jefferson County, Colorado

USGS Publications Warehouse

Adams, John W.; Stugard, Frederick

1954-01-01

Carbonate veins cutting pre-Cambrian metamorphic rocks in Golden Gate Canyon contain pitchblende and base-metal sulfides. The veins occupy extensive faults of Laramide age but normally contain pitchblende only where the cut hornblende gneiss. At the Union Pacific prospect, which was studied in detail, pitchblende, hermatite, and some ankerite formed in advance of sulfides, except possibly for minor pyrite. Base-metal sulfides and the bulk of ankerite-calcite vein-filling were deposited after the pitchblende. Chemical analyses show a high ferrous iron content in the hornblende gneiss in contrast to low ferrous iron in the adjacent biotite gneiss. It is hypothesized that ferrous iron released by alteration of hornblende was partly oxidized to hematite by the ore-bearing solutions and, contemporaneously, uranium was reduced and deposited as pitchblende. In other veins, biotite or iron sulfides may have been similarly effective in precipitating pitchblende. Apparently both the ferrous ion and the sulfide ion can serve as reducing agents and control pitchblende deposition. It is suggested that conditions particularly favorable for uranium deposition are present where uranium-bearing solutions had access to rocks rich in ferrous iron or pre-existing sulfides.

Long term contracts, expansion, innovation and stability: North Dakota's lignite mines thrive

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

Buchsbaum, L.

2009-08-15

North Dakota's lignite coal industry is mainly located in three countries in the central part of the state. Its large surface lignite mines are tied through long-term (20-40 years) contracts to power plants. The article talks about operations at three of the most productive mines - the Freedom mine, Falkirk mine and Center Mine. 4 figs.

Photochemical dissolution of Turkish lignites in tetralin at different irradiation power and reaction times

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

F. Karacan; T. Torul

2007-08-15

The effect of the power of ultraviolet (UV) irradiation on the tetrahydrofuran (THF) solubles yield (the total soluble product) and the soluble product distribution of the dissolution of Turkish lignites (Beypazari and Tuncbilek lignite) in tetralin at ambient temperatures has been investigated. The lignite samples were exposed to UV irradiation for 1, 2, 3, 5, and 10 days in the power of irradiation ranging from 0 to 180 W at 60 W intervals. The yields of THF solubles and oils increased with increasing irradiation power and time. The optimum irradiation power depends on the irradiation time to obtain the highestmore » degradation products. However, the yield of degradation products depends also on the lignite type. The largest fraction obtained from lignites by photochemical energy is oil. While the yields of THF solubles and oils sharply increased with irradiation power at longer reaction times, the yields of asphaltenes (AS) slightly decreased. Increasing oil yields is relatively larger when AS yields tend to decrease. These trends of AS and oil yields are ascribable to conversion of AS to oils at higher power. Small changes were observed in the PAS yields under all conditions. 27 refs., 5 figs., 1 tab.« less

H-binding of size- and polarity-fractionated soil and lignite humic acids after removal of metal and ash components.

PubMed

Drosos, Marios; Leenheer, Jerry A; Avgeropoulos, Apostolos; Deligiannakis, Yiannis

2014-03-01

A fractionation technique, combining dialysis removal of metal and ash components with hydrofluoric acid and pH 10 citrate buffer followed by chromatography of dialysis permeate on XAD-8 resin at decreasing pH values, has been applied to lignite humic acid (lignite-HA) and soil humic acid (soil-HA). H-binding data and non ideal competitive adsorption-Donnan model parameters were obtained for the HA fractions by theoretical analysis of H-binding data which reveal a significant increase of the carboxyl and the phenolic charge for the lignite-HA fractions vs. the parental lignite humic acid (LParentalHA). The fractionated lignite-HA material consisted mainly of permeate fractions, some of which were fulvic acid-like. The fractionated soil-HA material consisted mainly of large macromolecular structures that did not permeate the dialysis membrane during deashing. Chargeable groups had comparable concentrations in soil-HA fractions and parental soil humic acid (SParentalHA), indicating minimal interference of ash components with carboxyl and phenolic (and/or enolic) groups. Fractionation of HA, combined with theoretical analysis of H-binding, can distinguish the supramolecular vs. macromolecular nature of fractions within the same parental HA.

Activated-Lignite-Based Super Large Granular Slow-Release Fertilizers Improve Apple Tree Growth: Synthesis, Characterizations, and Laboratory and Field Evaluations.

PubMed

Tang, Yafu; Wang, Xinying; Yang, Yuechao; Gao, Bin; Wan, Yongshan; Li, Yuncong C; Cheng, Dongdong

2017-07-26

In this work, lignite, a low-grade coal, was modified using the solid-phase activation method with the aid of a Pd/CeO 2 nanoparticle catalyst to improve its pore structure and nutrient absorption. Results indicate that the adsorption ability of the activated lignite to NO 3 - , NH 4 + , H 2 PO 4 - , and K + was significantly higher than that of raw lignite. The activated lignite was successfully combined with the polymeric slow-release fertilizer, which exhibits typical slow-release behavior, to prepare the super large granular activated lignite slow-release fertilizer (SAF). In addition to the slow-release ability, the SAF showed excellent water-retention capabilities. Soil column leaching experiments further confirmed the slow-release characteristics of the SAF with fertilizer nutrient loss greatly reduced in comparison to traditional and slow-release fertilizers. Furthermore, field tests of the SAF in an orchard showed that the novel SAF was better than other tested fertilizers in improve the growth of young apple trees. Findings from this study suggest that the newly developed SAF has great potential to be used in apple cultivation and production systems in the future.

H-binding of size- and polarity-fractionated soil and lignite humic acids after removal of metal and ash components

USGS Publications Warehouse

Drosos, Marios; Leenheer, Jerry A.; Avgeropoulos, Apostolos; Deligiannakis, Yiannis

2014-01-01

A fractionation technique, combining dialysis removal of metal and ash components with hydrofluoric acid and pH 10 citrate buffer followed by chromatography of dialysis permeate on XAD-8 resin at decreasing pH values, has been applied to lignite humic acid (lignite-HA) and soil humic acid (soil-HA). H-binding data and non ideal competitive adsorption-Donnan model parameters were obtained for the HA fractions by theoretical analysis of H-binding data which reveal a significant increase of the carboxyl and the phenolic charge for the lignite-HA fractions vs. the parental lignite humic acid (LParentalHA). The fractionated lignite-HA material consisted mainly of permeate fractions, some of which were fulvic acid-like. The fractionated soil-HA material consisted mainly of large macromolecular structures that did not permeate the dialysis membrane during deashing. Chargeable groups had comparable concentrations in soil-HA fractions and parental soil humic acid (SParentalHA), indicating minimal interference of ash components with carboxyl and phenolic (and/or enolic) groups. Fractionation of HA, combined with theoretical analysis of H-binding, can distinguish the supramolecular vs. macromolecular nature of fractions within the same parental HA.

Uranium favorability of tertiary rocks in the Badger Flats, Elkhorn Thrust Area, Park and Teller Counties, Colorado

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

Young, P.; Mickle, D.G.

1976-10-01

Uranium potential of Tertiary rocks in the Badger Flats--Elkhorn Thrust area of central Colorado is closely related to a widespread late Eocene erosion surface. Most uranium deposits in the area are in the Eocene Echo Park Alluvium and Oligocene Tallahassee Creek Conglomerate, which were deposited in paleodrainage channels on or above this surface. Arkosic detritus within the channels and overlying tuffaceous sedimentary rocks of the Antero and Florissant Formations of Oligocene age and silicic tuffs within the volcanic units provide abundant sources of uranium that could be concentrated in the channels where carbonaceous debris facilitates a reducing environment. Anomalous soil,more » water, and stream-sediment samples near the Elkhorn Thrust and in Antero basin overlie buried channels or are offset from them along structural trends; therefore, uranium-bearing ground water may have moved upward from buried uranium deposits along faults. The area covered by rocks younger than the late Eocene erosion surface, specifically the trends of mapped or inferred paleochannels filled with Echo Park Alluvium and Tallahassee Creek Conglomerate, and the Antero Formation are favorable for the occurrence of uranium deposits.« less

Coal-bed methane potential in Montana

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

Campen, E.

1991-06-01

Montana's coal resources are the second largest of the US, with coal underlying approximately 35% of the state. These resources are estimated at 478 billion tons. Associated coal-bed methane resources are estimated to be 14 tcf. The coals of Montana range from Jurassic to early Tertiary in age and from lignite to low-volatile bituminous in rank. Thickness, rank, maceral composition, and proximate and ultimate analyses all vary vertically and laterally. The state contains eight major coal resource areas. A large percentage of Montana's coal consists of the Paleocene Fort Union lignites of eastern Montana, generally considered of too low amore » rank to contain significant methane resources. Most of the state's other coal deposits are higher in rank and contain many recorded methane shows. During Cretaceous and Tertiary times, regressive-transgressive cycles resulted in numerous coal-bearing sequences. Major marine regressions allowed the formation of large peat swamps followed by transgressions which covered the swamps with impervious marine shales, preventing the already forming methane from escaping. About 75% of Montana's coal is less than 1,000 ft below the ground's surface, making it ideal for methane production. Associated water appears to be fresh, eliminating environmental problems. Pipelines are near to most of the major coal deposits. Exploration for coal-bed methane in Montana is still in its infancy but at this time shows commercial promise.« less

Changes in floral composition with depositional environment in Texas Eocene Manning Formation lignites

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

Gennett, J.A.; Raymond, A.L.

1986-09-01

The floral composition of palynomorph assemblages of Jacksonian Texas lignites is closely linked to depositional systems. Localities on the eastern Gulf coastal plain are included in the late Eocene Fayette delta system, and lignite formation is considered to have occurred in lower deltaic environments. Samples are commonly dominated by grains of Caprifoliipites/Salixpollenites, Momites, or Nyssa, indicating dicotyledonous tree-dominated swamps. Some samples contain abundant Cicatricosspories spores, suggesting marshy, fern-dominated areas. The San Miguel lignite deposit in McMullen County is located on the eastern margin of the south Texas strand-plain/barrier-bar system. Caprifoliipites/Salixpollenites pollen is rare in the San Miguel, and most ofmore » the levels are dominated by small tricolporates such as cupuliferoipollenites and Sapotaceae. Nyssa is locally important. The lignite is considered to have been deposited in a nondeltaic freshwater swamp behind a barrier island. The Miguel Alleman deposit, across the Mexican border in Tamaulipas, is thought to have developed in a lagoonal-estuarine environment. Dinoflagellates such as Wetzeliella are common at some levels, indicating marine conditions. As with San Miguel, small tricolporates and Momipites are common. These assemblages contrast with Sabinian floras. Wilcox Group east Texas lignites were formed in fluvial environments. Betulaceous pollen is common in these coals. Sabinian south Texas lignites formed in marine environments yield dinoflagellates and Chenopodium-type pollen. Chenopods are common in present-day Gulf Coast salt marshes but seem to have been absent from Jackson-age seacoasts.« less

238U/235U determinations of some commonly used reference materials and U-bearing accessory minerals (Invited)

NASA Astrophysics Data System (ADS)

Condon, D.; Noble, S.; McLean, N.; Bowring, S. A.

2009-12-01

We have determined 238U/235U ratios for a suite of commonly used natural (CRM 112a, SRM 950a, HU-1) and synthetic (IRMM 184 and CRM U500) uranium reference materials in addition to several U-bearing accessory phases (zircon and monazite) by thermal ionisation mass-spectrometry (TIMS) using the IRMM 3636 233U-236U double spike to accurately correct for mass fractionation. The 238U/235U values for the natural uranium reference materials differ, by up to 0.1%, from the widely used ‘consensus’ value (137.88) with all having 238U/235U values less than 137.88. Similarly, initial 238U/235U data from zircon and monazite yield 238U/235U values that are lower than the ‘consensus’ value. The data obtained from U-bearing minerals is used to assess how the uncertainty in the 238U/235U ratio contributes to the systematic discordance observed in 238U/206Pb and 235U/207Pb dates (Mattinson, 2000; Schoene et al., 2006) which has traditionally been wholly attributed to error in the U decay constants. The 238U/235U determinations made on the synthetic reference materials yield results that are considerably more precise and accurate than the certified values (0.02% vs. 0.1% for CRM U500). The calibration of isotopic tracers used for U-daughter geochronology that are partially based upon these reference materials, and the resultant age determinations, will benefit from increased accuracy and precision. Mattinson, J.M., 2000. Revising the “gold standard”—the uranium decay constants of Jaffey et al., 1971. Eos Trans. AGU, Spring Meet. Suppl., Abstract V61A-02. Schoene B., Crowley J.L., Condon D.C., Schmitz M.D., Bowring S.A., 2006, Reassessing the uranium decay constants for geochronology using ID-TIMS U-Pb data. Geochimica et Cosmochimica Acta 70: 426-445

ELUTION OF URANIUM FROM RESIN

DOEpatents

McLEan, D.C.

1959-03-10

A method is described for eluting uranium from anion exchange resins so as to decrease vanadium and iron contamination and permit recycle of the major portion of the eluats after recovery of the uranium. Diminution of vanadium and iron contamination of the major portion of the uranium is accomplished by treating the anion exchange resin, which is saturated with uranium complex by adsorption from a sulfuric acid leach liquor from an ore bearing uranium, vanadium and iron, with one column volume of eluant prepared by passing chlorine into ammonium hydroxide until the chloride content is about 1 N and the pH is about 1. The resin is then eluted with 8 to 9 column volumes of 0.9 N ammonium chloride--0.1 N hydrochloric acid solution. The eluants are collected separately and treated with ammonia to precipitate ammonium diuranate which is filtered therefrom. The uranium salt from the first eluant is contaminated with the major portion of ths vanadium and iron and is reworked, while the uranium recovered from the second eluant is relatively free of the undesirable vanadium and irons. The filtrate from the first eluant portion is discarded. The filtrate from the second eluant portion may be recycled after adding hydrochloric acid to increase the chloride ion concentration and adjust the pH to about 1.

A review of Alabama lignite deposits

USGS Publications Warehouse

Aubourg, Claire E.; Warwick, Peter D.; Karlsen, Alexander K.; Merrill, Matthew D.; Valentine, Brett J.

2011-01-01

This review of Alabama lignite deposits is a part of the U.S. Geological Survey (USGS) National Coal Resource Assessment (NCRA) of the Gulf Coast region (see Ruppert et al., 2002; Dennen, 2009; and other chapters of this publication). Because lignite is not currently mined in Alabama, a detailed assessment of the state was not made, and only a review is presented in this chapter.

Coal geology of the Paleocene-Eocene Calvert Bluff Formation (Wilcox Group) and the Eocene Manning Formation (Jackson Group) in east-central Texas; field trip guidebook for the Society for Organic Petrology, Twelfth Annual Meeting, The Woodlands, Texas, August 30, 1995

USGS Publications Warehouse

Warwick, Peter D.; Crowley, Sharon S.

1995-01-01

The Jackson and Wilcox Groups of eastern Texas (fig. 1) are the major lignite producing intervals in the Gulf Region. Within these groups, the major lignite-producing formations are the Paleocene-Eocene Calvert Bluff Formation (Wilcox) and the Eocene Manning Formation (Jackson). According to the Keystone Coal Industry Manual (Maclean Hunter Publishing Company, 1994), the Gulf Coast basin produces about 57 million short tons of lignite annually. The state of Texas ranks number 6 in coal production in the United States. Most of the lignite is used for electric power generation in mine-mouth power plant facilities. In recent years, particular interest has been given to lignite quality and the distribution and concentration of about a dozen trace elements that have been identified as potential hazardous air pollutants (HAPs) by the 1990 Clean Air Act Amendments. As pointed out by Oman and Finkelman (1994), Gulf Coast lignite deposits have elevated concentrations of many of the HAPs elements (Be, Cd, Co, Cr, Hg, Mn, Se, U) on a as-received gm/mmBtu basis when compared to other United States coal deposits used for fuel in thermo-electric power plants. Although regulations have not yet been established for acceptable emissions of the HAPs elements during coal burning, considerable research effort has been given to the characterization of these elements in coal feed stocks. The general purpose of the present field trip and of the accompanying collection of papers is to investigate how various aspects of east Texas lignite geology might collectively influence the quality of the lignite fuel. We hope that this collection of papers will help future researchers understand the complex, multifaceted interrelations of coal geology, petrology, palynology and coal quality, and that this introduction to the geology of the lignite deposits of east Texas might serve as a stimulus for new ideas to be applied to other coal basins in the U.S. and abroad.

Uranium deposits in the Eureka Gulch area, Central City district, Gilpin County, Colorado

USGS Publications Warehouse

Sims, P.K.; Osterwald, F.W.; Tooker, E.W.

1954-01-01

The Eureka Gulch area of the Central City district, Gilpin County, Colo., was mined for ores of gold, silver, copper, lead, and zinc; but there has been little mining activity in the area since World War I. Between 1951 and 1953 nine radioactive mine dumps were discovered in the area by the U.S. Geological Survey and by prospectors. the importance of the discoveries has not been determined as all but one of the mines are inaccessible, but the distribution, quantity, and grade of the radioactive materials found on the mine dumps indicate that the area is worth of additional exploration as a possible source of uranium ore. The uranium ans other metals are in and near steeply dipping mesothermal veins of Laramide age intrusive rocks. Pitchblende is present in at least four veins, and metatorbernite, associated at places with kosolite, is found along two veins for a linear distance of about 700 feet. The pitchblends and metatorbernite appear to be mutually exclusive and seem to occur in different veins. Colloform grains of pitchblende were deposited in the vein essentially contemporaneously with pyrite. The pitchblende is earlier in the sequence of deposition than galena and sphalerite. The metatorbernite replaces altered biotite-quartz-plagioclase gneiss and altered amphibolite, and to a lesser extent forms coatings on fractures in these rocks adjacent to the veins; the kasolite fills vugs in highly altered material and in altered wall rocks. Much of the pitchblende found on the dumps has been partly leached subsequent to mining and is out of equilibrium. Selected samples of metatorbernite-bearing rock from one mine dump contain as much as 6.11 percent uranium. The pitchblende is a primary vein mineral deposited from uranium-bearing hydrothermal solutions. The metatorbernite probably formed by oxidation, solution, and transportation of uranium from primary pitchblende, but it may be a primary mineral deposited directly from fluids of different composition from these that deposited pitchblende.

Integrated geophysical investigations for the delineation of source and subsurface structure associated with hydro-uranium anomaly: A case study from South Purulia Shear Zone (SPSZ), India

NASA Astrophysics Data System (ADS)

Sharma, S. P.; Biswas, A.

2012-12-01

South Purulia Shear Zone (SPSZ) is an important region for prospecting of uranium mineralization. Geological studies and hydro-uranium anomaly suggest the presence of Uranium deposit around Raghunathpur village which lies about 8 km north of SPSZ. However, detailed geophysical investigations have not been carried out in this region for investigation of uranium mineralization. Since surface signature of uranium mineralization is not depicted near the location, a deeper subsurface source is expected for hydro uranium anomaly. To delineate the subsurface structure and to investigate the origin of hydro-uranium anomaly present in the area, Vertical Electrical Sounding (VES) using Schlumberger array and Gradient Resistivity Profiling (GRP) were performed at different locations along a profile perpendicular to the South Purulia Shear Zone. Apparent resistivity computed from the measured sounding data at various locations shows a continuously increasing trend. As a result, conventional apparent resistivity data is not able to detect the possible source of hydro uranium anomaly. An innovative approach is applied which depicts the apparent conductivity in the subsurface revealed a possible connection from SPSZ to Raghunathpur. On the other hand resistivity profiling data suggests a low resistive zone which is also characterized by low Self-Potential (SP) anomaly zone. Since SPSZ is characterized by the source of uranium mineralization; hydro-uranium anomaly at Raghunathpur is connected with the SPSZ. The conducting zone has been delineated from SPSZ to Raghunathpur at deeper depths which could be uranium bearing. Since the location is also characterized by a low gravity and high magnetic anomaly zone, this conducting zone is likely to be mineralized zone. Keywords: Apparent resistivity; apparent conductivity; Self Potential; Uranium mineralization; shear zone; hydro-uranium anomaly.

Depositional environments of the uranium-bearing Cutler Formations, Lisbon Valley, Utah

USGS Publications Warehouse

Campbell, John A.; Steele-Mallory, Brenda A.

1979-01-01

The Cutler Formation in Lisbon Valley, San Juan County, Utah, is composed predominantly of fluvial arkosic sandstones, siltstones, shales, and mudstones that were deposited by meandering streams that flowed across a flood plain and tidal flat close to sea level. Two types of channel deposits are recognized from their sedimentary structures: meandering and distributary. The flood plain was occasionally transgressed by a shallow sea from the west, resulting in the deposition of several thin limestones and marine sandstones. The marine sandstones were deposited as longshore bars. Wind transported sand along the shoreline of the shallow sea, forming a coastal dune field. Marine sandstones and eolian sandstones are more common in the upper Cutler in the southern part of the area, whereas in the central and northern part of the area the formation is predominantly fluvial. Crossbed orientation indicates that Cutler streams flowed S. 67? W. on the the average, whereas marine currents moved sediment S. 36? E. and N. 24? W., and wind transported sand S. 800 E. The uranium in the Cutler is found in the central and northern part of the area, in the upper part of the formation, in small fluvial sandstone bodies that were deposited predominantly in a distributary environment. No uranium is known in the marine or eolian sandstones. Petrographically, the uranium-bearing sandstones are identical to other Cutler fluvial sandstones except that they contain less calcite and more clay and are slightly coarser grained. Ore formation has modified the host sandstones very little.

Exploration for uranium deposits in the Atkinson Mesa area, Montrose County, Colorado

USGS Publications Warehouse

Brew, Daniel Allen

1954-01-01

The U.S. Geological Survey explored the Atkinson Mesa area for uranium- and vanadium-bearing deposits from July 2, 1951, to June 18, 1953, with 397 diamond-drill holes that totaled 261,251 feet. Sedimentary rocks of Mesozoic age are exposed in the Atkinson Mesa area. They are: the Brushy Basin member of the Upper Jurassic Morrison formation, the Lower Cretaceous Burro Canyon formation, and the Upper and Lower Cretaceous Dakota sandstone. All of the large uranium-vanadium deposits discovered by Geological Survey drilling are in a series of sandstone lenses in the upper part of the Salt Wash member of the Jurassic Morrison formation. The deposits are mainly tabular and blanket-like, but some elongate pod-shaped masses, locally called "rolls" may be present. The mineralized material consists of sandstone impregnated with a uranium mineral which is probably coffinite, spme carnotite, and vanadium minerals, thought to be mainly corvusite and montroseite. In addition,, some mudstone and carbonaceous material is similarly impregnated. Near masses of mineralized material the sandstone is light gray or light brown, is generally over 40 feet thick, and usually contains some carbonaceous material and abundant disseminated pyrite or limonite stain. Similarly, the mudstone in contact with the ore-bearing sandstone near bodies of mineralized rock is commonly blue gray, as compared to its dominant red color away from ore deposits. Presence and degree of these features are useful guides in exploring for new deposits.

Bioprocessing of lignite coals using reductive microorganisms

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

Crawford, D.L.

In order to convert lignite coals into liquid fuels, gases or chemical feedstock, the macromolecular structure of the coal must be broken down into low molecular weight fractions prior to further modification. Our research focused on this aspect of coal bioprocessing. We isolated, characterized and studied the lignite coal-depolymerizing organisms Streptomyces viridosporus T7A, Pseudomonas sp. DLC-62, unidentified bacterial strain DLC-BB2 and Gram-positive Bacillus megaterium strain DLC-21. In this research we showed that these bacteria are able to solubilize and depolymerize lignite coals using a combination of biological mechanisms including the excretion of coal solublizing basic chemical metabolites and extracellular coalmore » depolymerizing enzymes.« less

Carbon-free induction furnace

DOEpatents

Holcombe, Cressie E.; Masters, David R.; Pfeiler, William A.

1985-01-01

An induction furnace for melting and casting highly pure metals and alloys such as uranium and uranium alloys in such a manner as to minimize contamination of the melt by carbon derived from the materials and the environment within the furnace. The subject furnace is constructed of carbon free materials and is housed within a conventional vacuum chamber. The furnace comprises a ceramic oxide crucible for holding the charge of metal or alloy. The heating of the crucible is achieved by a plasma-sprayed tungsten susceptor surrounding the crucible which, in turn, is heated by an RF induction coil separated from the susceptor by a cylinder of inorganic insulation. The furnace of the present invention is capable of being rapidly cycled from ambient temperatures to about 1650.degree. C. for effectively melting uranium and uranium alloys without the attendant carbon contamination problems previously encountered when using carbon-bearing furnace materials.

Non-carbon induction furnace

DOEpatents

Holcombe, C.E.; Masters, D.R.; Pfeiler, W.A.

1984-01-06

The present invention is directed to an induction furnace for melting and casting highly pure metals and alloys such as uranium and uranium alloys in such a manner as to minimize contamination of the melt by carbon derived from the materials and the environment within the furnace. The subject furnace is constructed of non-carbon materials and is housed within a conventional vacuum chamber. The furnace comprises a ceramic oxide crucible for holding the charge of metal or alloys. The heating of the crucible is achieved by a plasma-sprayed tungsten susceptor surrounding the crucible which, in turn, is heated by an rf induction coil separated from the susceptor by a cylinder of inorganic insulation. The furnace of the present invention is capable of being rapidly cycled from ambient temperatures to about 1650/sup 0/C for effectively melting uranium and uranium alloys without the attendant carbon contamination problems previously encountered when using carbon-bearing furnace materials.

Uranium hydrogeochemical and stream sediment reconnaissance of the Newcastle NTMS Quadrangle, Wyoming, including concentrations of forty-two additional elements

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

Goff, S.J.; Sandoval, W.F.; Gallimore, D.L.

1980-06-01

Water and sediment samples were collected and each water sample was analyzed for U, and each sediment sample was analyzed for 43 elements, including U and Th. Uranium concentrations in water samples range from below the detection limit of 0.02 ppB to 702.26 ppB and have a median of 1.73 ppB and a mean of 11.76 ppB. Water samples containing high uranium concentrations generally are associated with known uranium mining activity or units known to be uranium bearing. About one-third of the water samples containing high uranium concentrations were collected from locations within the Pumpkin Buttes and Turnercrest-Ross Districts. Nearlymore » half of the water samples containing high uranium concentrations were collected from locations just west of the Monument Hill and Highland Flats-Box Creek Districts. Similar anomalous uranium concentrations in this region have been reported updip from Exxon's Highland uranium deposits. High uranium concentrations were also found associated with the Lance Creek-Old Woman Anticline District. Uranium concentrations in sediment samples range from 1.14 to 220.70 ppM and have a median of 3.37 ppM and a mean of 4.03 ppM. Throughout the major uranium mining districts of the Powder River Basin, sediment samples with high uranium concentrations were collected from dry streams located near wells producing water samples with high uranium concentrations. High uranium concentrations were also found associated with the Lance Creek oil field where uranium mineralization is known in the White River formation. High uranium concentrations were also found in sediment samples in areas where uranium mineralization is not known. These samples are from dry streams in areas underlain by the White River formation, the Niobrara formation, and the Pierre, Carlisle, Belle Fourche, and Mowry shales.« less

Co-combustion of pellets from Soma lignite and waste dusts of furniture works

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

Deveci, N.D.; Yilgin, M.; Pehlivan, D.

2008-07-01

In this work, volatiles and char combustion behaviors of the fuel pellets prepared from a low quality lignite and the dusts of furniture works and their various blends were investigated in an experimental fixed bed combustion system through which air flowed by natural convection. Combustion data obtained for varied bed temperatures, mass of pellets, and blend compositions has showed that ignition times of the pellets decreased and volatiles combustion rates tended to increase with the burning temperature. It was concluded that some synergy had existed between lignite and lower ratios of furniture work dusts, which was indicated by a promptmore » effect on the volatiles combustion rates. Char combustion rates of blend pellets have depended predominantly on the amount of lignite in the blend. The amounts of combustion residues of the pellets were considerably higher than those calculated from individual ash contents of the raw materials and related to lignite ratio in the blends.« less

Interactions between organic amendments and phosphate fertilizers modify phosphate sorption processes in an acid soil

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

Sckefe, C.R.; Patti, A.F.; Clune, T.S.

2008-07-15

To determine how organic amendments and phosphate fertilizers interact to modify P sorption processes, three phosphate fertilizers were applied to lignite- and compost-amended acid soil and incubated for either 3 or 26 days. The fertilizers applied were potassium dihydrogen phosphate, triple superphosphate, and diammonium phosphate (DAP). After 3 days of incubation, sorption of all three P sources was decreased in the lignite-amended treatments, whereas P sorption was increased in the compost-amended treatments. Increased incubation time (26 days) resulted in significantly decreased P sorption when DAP was added to lignite-amended treatments. Addition of triple superphosphate increased P sorption in lignite- andmore » compost-amended treatments and decreased solution pH compared with DAP application. In addition to the effect of P source, differences in P sorption between the lignite- and compost-amended treatments were driven by differences in solution chemistry, predominantly solution pH and cation dynamics. Soil amendment and fertilizer addition also increased microbial activity in the incubation systems, as measured by carbon dioxide respiration. It is proposed that the combination of lignite and DAP may contribute to decreased P sorption in acid soils, with the positive effects likely caused by both chemical and biological processes, including the formation of soluble organic-metal complexes.« less

Process Analysis of Lignite Circulating Fluidized Bed Boiler Coupled with Pyrolysis Topping

NASA Astrophysics Data System (ADS)

Wang, Baoqun; Dong, Li; Wang, Yin; Matsuzawa, Y.; Xu, Guangwen

We developed a comprehensive process model in ASPEN Plus to simulate the energy and mass balances of a lignite-fueled atmospheric circulating fluidized bed (CFB) boiler integrated with coal predrying and pyrolysis topping. In this model, it is assumed that the heat from exhausted flue gas was employed for coal predrying, and the sensible heat derived from circulated bed material was used for the pyrolysis topping (endothermic process). The simulation was conducted with respectto the Yunnan Kaiyuan CFB boiler, and two representative lignite coals from Xiao Long Tan (XLT) and Xin Shao (XS) were considered. The result shows that the predrying of coal with the sensible heat of above 363 K from flue gas, the amount of coal consumed in the boiler can be reduced by 3.5% and 5.3% for XLT lignite and XS lignite, respectively. It was also found that integration of pyrolysis topping with the boiler increased the coal consumption of the boiler, and the extent of consumption-increase varies with the yields of tar and gas in the pyrolysis topping process. For agas yield of 5.2% and a tar yield of 5-6%, the consumption of XS lignite increased by about 20% comparing to that in the case without topping.

Adsorption Behavior of Surfactant on Lignite Surface: A Comparative Experimental and Molecular Dynamics Simulation Study

PubMed Central

He, Meng; Zhang, Wei; Cao, Xiaoqiang; You, Xiaofang; Li, Lin

2018-01-01

Experimental and computational simulation methods are used to investigate the adsorption behavior of the surfactant nonylphenol ethoxylate (NPEO10), which contains 10 ethylene oxide groups, on the lignite surface. The adsorption of NPEO10 on lignite follow a Langmuir-type isotherm. The thermodynamic parameters of the adsorption process show that the whole process is spontaneous. X-ray photoelectron spectroscopic (XPS) analysis indicates that a significant fraction of the oxygen-containing functional groups on the lignitic surface were covered by NPEO10. Molecular dynamics (MD) simulations show that the NPEO10 molecules were found to adsorb at the water-coal interface. Moreover, polar interactions are the main effect in the adsorption process. The density distributions of coal, NPEO10, and water molecules along the Z axis show that the remaining hydrophobic portions of the surfactant extend into the solution, creating a more hydrophobic coal surface that repels water molecules. The negative interaction energy calculated from the density profiles of the head and tail groups along the three spatial directions between the surfactant and the lignitic surface suggest that the adsorption process is spontaneous. The self-diffusion coefficients show that the presence of NPEO10 causes higher water mobility by improving the hydrophobicity of lignite. PMID:29389899

Irradiation performance of HTGR fuel rods in HFIR experiments HRB-7 and -8

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

Valentine, K.H.; Homan, F.J.; Long, E.L. Jr.

1977-05-01

The HRB-7 and -8 experiments were designed as a comprehensive test of mixed thorium-uranium oxide fissile particles with Th:U ratios from 0 to 8 for HTGR recycle application. In addition, fissile particles derived from Weak-Acid Resin (WAR) were tested as a potential backup type of fissile particle for HTGR recycle. These experiments were conducted at two temperatures (1250 and 1500/sup 0/C) to determine the influence of operating temperature on the performance parameters studied. The minor objectives were comparison of advanced coating designs where ZrC replaced SiC in the Triso design, testing of fuel coated in laboratory-scale equipment with fuel coatedmore » in production-scale coaters, comparison of the performance of /sup 233/U-bearing particles with that of /sup 235/U-bearing particles, comparison of the performance of Biso coatings with Triso coatings for particles containing the same type of kernel, and testing of multijunction tungsten-rhenium thermocouples. All objectives were accomplished. As a result of these experiments the mixed thorium-uranium oxide fissile kernel was replaced by a WAR-derived particle in the reference recycle design. A tentative decision to make this change had been reached before the HRB-7 and -8 capsules were examined, and the results of the examination confirmed the accuracy of the previous decision. Even maximum dilution (Th/U approximately equal to 8) of the mixed thorium-uranium oxide kernel was insufficient to prevent amoeba of the kernels at rates that are unacceptable in a large HTGR. Other results showed the performance of /sup 233/U-bearing particles to be identical to that of /sup 235/U-bearing particles, the performance of fuel coated in production-scale equipment to be at least as good as that of fuel coated in laboratory-scale coaters, the performance of ZrC coatings to be very promising, and Biso coatings to be inferior to Triso coatings relative to fission product retention.« less

Radioactive deposits in California

USGS Publications Warehouse

Walker, George W.; Lovering, Tom G.

1954-01-01

Reconnaissance examination by Government geologists of many areas, mine properties, and prospects in California during the period between 1948 and 1953 has confirmed the presence of radioactive materials in place at more than 40 localities. Abnormal radioactivity at these localities is due to concentrations of primary and secondary uranium minerals, to radon gas, radium (?), and to thorium minerals. Of the known occurrences only three were thought to contain uranium oxide (uranitite or pitchblende), 4 contained uranium-bearing columbate, tantalate, or titanate minerals, 12 contained secondary uranium minerals, such as autunite, carnotite, and torbernite, one contained radon gas, 7 contained thorium minerals, and, at the remaining 16 localities, the source of the anomalous radiation was not positively determined. The occurrences in which uranium oxide has been tentatively identified include the Rathgeb mine (Calaveras County), the Yerih group of claims (San Bernardino County), and the Rainbow claim (Madera County). Occurrences of secondary uranium minerals are largely confined to the arid desert regions of south-eastern California including deposits in San Bernardino, Kern, Inyo, and Imperial Counties. Uranium-bearing columbate, tantalate, or titanate minerals have been reported from pegmatite and granitic rock in southeastern and eastern California. Thorium minerals have been found in vein deposits in eastern San Bernardino County and from pegmatites and granitic rocks in various parts of southeastern California; placer concentrations of thorium minerals are known from nearly all areas in the State that are underlain, in part, by plutonic crystalline rocks. The primary uranium minerals occur principally as minute accessory crystals in pegmatite or granitic rock, or with base-metal sulfide minerals in veins. Thorium minerals also occur as accessory crystals in pegmatite or granitic rock, in placer deposits derived from such rock, and, at Mountain Pass, in veins containing rare earths. Secondary uranium minerals have been found as fracture coatings and as disseminations in various types of wall rock, although they are largely confined to areas of Tertiary volcanic rocks. Probably the uranium in the uraniferous deposits in California is related genetically to felsic crystalline rocks and felsic volcanic rocks; the present distribution of the secondary uranium minerals has been controlled, in part, by circulating ground waters and probably, in part, by magmatic waters related to the Tertiary volcanic activity. The thorium minerals are genetically related to the intrusion of pegmatite and plutonic crystalline rocks. None of the known deposits of radioactive minerals in California contain marketable reserves of uranium or thorium ore under economic conditions existing in 1952. With a favorable local market small lots of uranium ore may be available in the following places: the Rosamund prospect, the Rafferty and Chilson properties, the Lucky Star claim, and the Yerih group. The commercial production of thorium minerals will be possible, in the near future, only if these minerals can be recovered cheaply as a byproduct either from the mining of rare earths minerals at Mountain Pass or as a byproduct of placer mining for gold.

Bioprocessing of lignite coals using reductive microorganisms. Final technical report, September 30, 1988--March 29, 1992

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

Crawford, D.L.

In order to convert lignite coals into liquid fuels, gases or chemical feedstock, the macromolecular structure of the coal must be broken down into low molecular weight fractions prior to further modification. Our research focused on this aspect of coal bioprocessing. We isolated, characterized and studied the lignite coal-depolymerizing organisms Streptomyces viridosporus T7A, Pseudomonas sp. DLC-62, unidentified bacterial strain DLC-BB2 and Gram-positive Bacillus megaterium strain DLC-21. In this research we showed that these bacteria are able to solubilize and depolymerize lignite coals using a combination of biological mechanisms including the excretion of coal solublizing basic chemical metabolites and extracellular coalmore » depolymerizing enzymes.« less

Microbial screening test for lignite degradation. Quarterly progress report No. 3, July 1-September 30, 1985

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

Yen, T.F.

1985-01-01

Degradation of Beulah std No. 3 lignite was carried out by means of cupric oxidation, modified-autoclaved-cupric oxidation, sodium dichromate oxidation, and also by biological methods. Assessment of the yield of alkaline-soluble and methanol soluble products of both cupric oxidation and modified cupric oxidation (on a moisture-free and ash-free basis) was carried out by both ion chromatography and gel permeation chromatography. Fractionation of lignite for natural-uninoculated-biological growth resulted in no growth for both benzene-methanol fraction and alkaline filtrate fraction, whereas that of alkaline geletinous fraction resulted in positive growth of unidentified white-rot fungi. Acclimation of Polyporus versicolor to lignite was attempted.more » 10 refs.« less

Radon gas: contractor liability for an indoor health hazard.

PubMed

Shuko, C M

1986-01-01

Many families throughout the United States have recently detected dangerously high concentrations of radon gas inside their homes. Radon, a carcinogenic gas produced from uranium, has been discovered in structures overlying uranium-bearing rock. This discovery may result in litigation to determine contractor liability for building upon radon-releasing rock sites. This Note examines the strengths and weaknesses of the various theories of contractor liability and considers potential statutory claims under the Clean Air Act. The Note suggests, as an alternative approach to recovery, a proposed regulatory scheme and implementation plan.

U-Th-Pb systematics of some granitoids from the northeastern Yilgarn Block, Western Australia and implications for uranium source rock potential.

USGS Publications Warehouse

Stuckless, J.S.; Bunting, J.A.; Nkomo, I.T.

1981-01-01

The Mount Boreas-type granite and spatially associated syenitic granitoid of Western Australia yield Pb/Pb ages of 2370+ or -100Ma and 2760+ or -210Ma, respectively. Th/Pb ages, although less precise, are concordant with these ages, and therefore the apparent ages are interpreted to be the crystallisation ages for these two units. U/Pb ages are variable and for the most part anomalously old, which suggests a Cainozoic uranium loss. However, this loss is generally small (<3mu g/g); therefore, neither granitoid in its fresh state provides a good source for nearby calcrete-hosted uranium deposits. The possibility remains that the Mount Boreas- type granite that has been completely weathered during the Tertiary could have been a source for the calcrete-type uranium deposits in W.A. Although the Mount Boreas-type granite is highly fractionated, it does not bear a strong geochemical imprint of a sedimentary precursor. This feature contrasts it with apparently fresh granitoids from other parts of the world that have lost large amounts of uranium (approx 20mu g/g) and are associated with large roll-type and other low temperature-type uranium deposits.-Authors

Infrared spectra and quantum chemical calculations of the uranium-carbon molecules UC, CUC, UCH, and U(CC)2

NASA Astrophysics Data System (ADS)

Wang, Xuefeng; Andrews, Lester; Ma, Dongxia; Gagliardi, Laura; Gonçalves, António P.; Pereira, Cláudia C. L.; Marçalo, Joaquim; Godart, Claude; Villeroy, Benjamin

2011-06-01

Laser evaporation of carbon rich uranium/carbon alloy targets into condensing argon or neon matrix samples gives weak infrared absorptions that increase on annealing, which can be assigned to new uranium carbon bearing species. New bands at 827.6 cm-1 in solid argon or 871.7 cm-1 in neon become doublets with mixed carbon 12 and 13 isotopes and exhibit the 1.0381 carbon isotopic frequency ratio for the UC diatomic molecule. Another new band at 891.4 cm-1 in argon gives a three-band mixed isotopic spectrum with the 1.0366 carbon isotopic frequency ratio, which is characteristic of the anti-symmetric stretching vibration of a linear CUC molecule. No evidence was found for the lower energy cyclic U(CC) isomer. Other bands at 798.6 and 544.0 cm-1 are identified as UCH, which has a uranium-carbon triple bond similar to that in UC. Evidence is found for bicyclic U(CC)2 and tricyclic U(CC)3. This work shows that U and C atoms react spontaneously to form the uranium carbide U≡C and C≡U≡C molecules with uranium-carbon triple bonds.

Possible linkages between lignite aquifers, pathogenic microbes, and renal pelvic cancer in northwestern Louisiana, USA

USGS Publications Warehouse

Bunnell, J.E.; Tatu, C.A.; Bushon, R.N.; Stoeckel, D.M.; Brady, A.M.G.; Beck, M.; Lerch, H.E.; McGee, B.; Hanson, B.C.; Shi, R.; Orem, W.H.

2006-01-01

In May and September, 2002, 14 private residential drinking water wells, one dewatering well at a lignite mine, eight surface water sites, and lignite from an active coal mine were sampled in five Parishes of northwestern Louisiana, USA. Using a geographic information system (GIS), wells were selected that were likely to draw water that had been in contact with lignite; control wells were located in areas devoid of lignite deposits. Well water samples were analyzed for pH, conductivity, organic compounds, and nutrient and anion concentrations. All samples were further tested for presence of fungi (cultures maintained for up to 28 days and colonies counted and identified microscopically) and for metal and trace element concentration by inductively-coupled plasma mass spectrometry and atomic emission spectrometry. Surface water samples were tested for dissolved oxygen and presence of pathogenic leptospiral bacteria. The Spearman correlation method was used to assess the association between the endpoints for these field/laboratory analyses and incidence of cancer of the renal pelvis (RPC) based on data obtained from the Louisiana Tumor Registry for the five Parishes included in the study. Significant associations were revealed between the cancer rate and the presence in drinking water of organic compounds, the fungi Zygomycetes, the nutrients PO4 and NH3, and 13 chemical elements. Presence of human pathogenic leptospires was detected in four out of eight (50%) of the surface water sites sampled. The present study of a stable rural population examined possible linkages between aquifers containing chemically reactive lignite deposits, hydrologic conditions favorable to the leaching and transport of toxic organic compounds from the lignite into the groundwater, possible microbial contamination, and RPC risk. ?? Springer Science+Business Media B.V. 2006.

Deaths from neoplasms and detection of radionuclides in excised human lungs in the Eordea Basin, Greece.

PubMed

Sichletidis, Lazaros T; Tsiotsios, Ioannis; Gavriilidis, Agapios; Chloros, Diamantis; Konstantinidis, Theodoros; Psarrakos, Kiriakos; Koufogiannis, Dimitrios; Siountas, Anastasios; Filippou, Dimitrios

2003-12-01

Lignite contains various trace-metal natural radioactive contaminants. In the Eordea Basin, the most important lignite field in Greece, the authors conducted a proportional mortality ratio (PMR) study that compared the mortality rates of individuals who lived in the basin vs. a control group who resided in the city of Kilkis, over a 30-yr period. The following information was used in the study: (a) municipal registrations of deaths from neoplasms during the period from 1971 to 2000, and (b) detection of radioactive substances in samples obtained from excised lungs of individuals living in Eordea Basin who suffered from neoplasm. The corresponding registrations of deaths from neoplasm of the inhabitants of Kilkis, a city located outside the Eordea Basin, formed the control group. A diachronic increase of the PMR was detected as a result of neoplasms and, particularly, as a result of lung cancer in Eordea Basin. However, the above ratio did not exceed the corresponding PMR recorded in Kilkis. In 20 lung samples obtained from patients who had lived in Eordea Basin, and in 19 lung samples from patients in Kilkis, the activity of the radionuclides of uranium and thorium radioactive decay series, potassium-40, and cesium-137 was not higher than expected. No statistically significant difference was found between the inhabitants of the 2 regions, thus it was concluded that the increase in respiratory-system neoplasms was likely associated with the high prevalence of smoking among the regions' inhabitants. In future studies, a longer observation period and examination of more cases will be necessary to further investigate a possible association between radionuclides and lung neoplasms in the Eordea Basin.

Determination of particle-bound polycyclic aromatic hydrocarbons emitted from co-pelletization combustion of lignite and rubber wood sawdust

NASA Astrophysics Data System (ADS)

Kan, R.; Kaosol, T.; Tekasakul, P.; Tekasakul, S.

2017-09-01

Determination of particle-bound Polycyclic Aromatic Hydrocarbons (PAHs) emitted from co-pelletization combustion of lignite and rubber wood sawdust in a horizontal tube furnace is investigated using High Performance Liquid Chromatography with coupled Diode Array and Fluorescence Detection (HPLC-DAD/FLD). The particle-bound PAHs based on the mass concentration and the toxicity degree are discussed in the different size ranges of the particulate matters from 0.07-11 μm. In the present study, the particle-bound PAHs are likely abundant in the fine particles. More than 70% of toxicity degree of PAHs falls into PM1.1 while more than 80% of mass concentration of PAHs falls into PM2.5. The addition of lignite amount in the co-pelletization results in the increasing concentration of either 4-6 aromatic ring PAHs or high molecular weight PAHs. The high contribution of 4-6 aromatic ring PAHs or high molecular weight PAHs in the fine particles should be paid much more attention because of high probability of human carcinogenic. Furthermore, the rubber wood sawdust pellets emit high mass concentration of PAHs whereas the lignite pellets emit high toxicity degree of PAHs. By co-pelletized rubber wood sawdust with lignite (50% lignite pellets) has significant effect to reduce the toxicity degree of PAHs by 70%.

Factors controlling localization of uranium deposits in the Dakota Sandstone, Gallup and Ambrosia Lake mining districts, McKinley County, New Mexico

USGS Publications Warehouse

Pierson, Charles Thomas; Green, Morris W.

1977-01-01

Geologic studies were made at all of the uranium mines and prospects in the Dakota Sandstone of Early(?) and Late Cretaceous age in the Gallup mining district, McKinley County, New Mexico. Dakota mines in the adjacent Ambrosia Lake mining district were visited briefly for comparative purposes. Mines in the eastern part of the Gallup district, and in the Ambrosia Lake district, are on the Chaco slope of the southern San Juan Basin in strata which dip gently northward toward the central part of the basin. Mines in the western part of the Gallup district are along the Gallup hogback (Nutria monocline) in strata which dip steeply westward into the Gallup sag. Geologic factors which controlled formation of the uranium deposits in the Dakota Sandstone are: (1) a source of uranium, believed to be uranium deposits of the underlying Morrison Formation of Late Jurassic age; (2) the accessibility to the Dakota of uranium-bearing solutions from the Morrison; (3) the presence in the Dakota of permeable sandstone beds overlain by impermeable carbonaceous shale beds; and (4) the occurrence within the permeable Dakota sandstone beds of carbonaceous reducing material as bedding-plane laminae, or as pockets of carbonaceous trash. Most of the Dakota uranium deposits are found in the lower part of the formation in marginal-marine distributary-channel sandstones which were deposited in the backshore environment. However, the Hogback no. 4 (Hyde) Mine (Gallup district) occurs in sandy paludal shale of the backshore environment, and another deposit, the Silver Spur (Ambrosia Lake district), is found in what is interpreted to be a massive beach or barrier-bar sandstone of the foreshore environment in the upper part of the Dakota. The sedimentary depositional environment most favorable for the accumulation of uranium is that of backshore areas lateral to main distributary channels, where levee, splay, and some distributary-channel sandstones intertongue with gray carbonaceous shales and siltstones of the well-drained swamp environment. Deposits of black carbonaceous shale which were formed in the poorly drained swamp deposits of the interfluve area are not favorable host rocks for uranium. The depositional energy levels of the various environments in which the sandstone and shale beds of the Dakota were deposited govern the relative favorability of the strata as uranium host rocks. In the report area, uranium usually occurs in carbonaceous sandstone deposited under low- to medium-energy fluvial conditions within distributary channels. A prerequisite, however, is that such sandstone be overlain by impermeable carbonaceous shale beds. Low- to medium-energy fluvial conditions result in the deposition of sandstone beds having detrital carbonaceous material distributed in laminae or in trash pockets on bedding planes. The carbonaceous laminae and trash pockets provide the necessary reductant to cause precipitation of uranium from solution. High-energy fluvial conditions result in the deposition of sandstones having little or no carbonaceous material included to provide a reductant. Very low energy swampy conditions result in carbonaceous shale deposits, which are generally barren of uranium because of their relative impermeability to migrating uranium-bearing solutions.

Cofiring lignite with hazelnut shell and cotton residue in a pilot-scale fluidized bed combustor

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

Zuhal Gogebakan; Nevin Selcuk

In this study, cofiring of high ash and sulfur content lignite with hazelnut shell and cotton residue was investigated in 0.3 MWt METU Atmospheric Bubbling Fluidized Bed Combustion (ABFBC) Test Rig in terms of combustion and emission performance of different fuel blends. The results reveal that cofiring of hazelnut shell and cotton residue with lignite increases the combustion efficiency and freeboard temperatures compared to those of lignite firing with limestone addition only. CO{sub 2} emission is not found sensitive to increase in hazelnut shell and cotton residue share in fuel blend. Cofiring lowers SO{sub 2} emissions considerably. Cofiring of hazelnutmore » shell reduces NO and N{sub 2}O emissions; on the contrary, cofiring cotton residue results in higher NO and N{sub 2}O emissions. Higher share of biomass in the fuel blend results in coarser cyclone ash particles. Hazelnut shell and cotton residue can be cofired with high ash and sulfur-containing lignite without operational problems. 32 refs., 12 figs., 11 tabs.« less

Combustion characteristics and air pollutant formation during oxy-fuel co-combustion of microalgae and lignite.

PubMed

Gao, Yuan; Tahmasebi, Arash; Dou, Jinxiao; Yu, Jianglong

2016-05-01

Oxy-fuel combustion of solid fuels is seen as one of the key technologies for carbon capture to reduce greenhouse gas emissions. The combustion characteristics of lignite coal, Chlorella vulgaris microalgae, and their blends under O2/N2 and O2/CO2 conditions were studied using a Thermogravimetric Analyzer-Mass Spectroscopy (TG-MS). During co-combustion of blends, three distinct peaks were observed and were attributed to C. vulgaris volatiles combustion, combustion of lignite, and combustion of microalgae char. Activation energy during combustion was calculated using iso-conventional method. Increasing the microalgae content in the blend resulted in an increase in activation energy for the blends combustion. The emissions of S- and N-species during blend fuel combustion were also investigated. The addition of microalgae to lignite during air combustion resulted in lower CO2, CO, and NO2 yields but enhanced NO, COS, and SO2 formation. During oxy-fuel co-combustion, the addition of microalgae to lignite enhanced the formation of gaseous species. Copyright © 2016 Elsevier Ltd. All rights reserved.

Lignite deposits of the Kutch Basin, western India: Carbon isotopic and palynological signatures of the early Eocene hyperthermal event ETM2

NASA Astrophysics Data System (ADS)

Agrawal, Shailesh; Verma, Poonam; Rao, M. R.; Garg, Rahul; Kapur, Vivesh V.; Bajpai, Sunil

2017-09-01

This study presents new results of combined palynological and stable carbon isotope (δ13C) investigations carried out in the well known lignite sequence at Panandhro, District Kutch, in the Gujarat state of western India. Dinoflagellate cysts and associated spore-pollen assemblage assign an early Eocene (Ypresian) age to the lignitic succession at Panandhro. Furthermore, a pronounced negative Carbon Isotope Excursion (CIE) of about 2.7‰, correlated to the Second Eocene Thermal Maximum (53.7 Ma), a globally recognized hyperthermal event, was discovered in the middle part of the succession, consistent with the palynological constraints. This is the first record of an Eocene hyperthermal event (ETM2) from the Kutch Basin. Our data has regional implications for the age of the lignitic sequences across western India as it demonstrates that there is no significant age difference between the lignite deposits of the Kutch and Cambay basins. Our results also support a Lutetian age for the previously described vertebrate fossils, including whales, from the Panandhro mine section.

Application of neodymium isotope ratio measurements for the origin assessment of uranium ore concentrates.

PubMed

Krajkó, Judit; Varga, Zsolt; Yalcintas, Ezgi; Wallenius, Maria; Mayer, Klaus

2014-11-01

A novel procedure has been developed for the measurement of (143)Nd/(144)Nd isotope ratio in various uranium-bearing materials, such as uranium ores and ore concentrates (UOC) in order to evaluate the usefulness and applicability of variations of (143)Nd/(144)Nd isotope ratio for provenance assessment in nuclear forensics. Neodymium was separated and pre-concentrated by extraction chromatography and then the isotope ratios were measured by multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS). The method was validated by the measurement of standard reference materials (La Jolla, JB-2 and BCR-2) and the applicability of the procedure was demonstrated by the analysis of uranium samples of world-wide origin. The investigated samples show distinct (143)Nd/(144)Nd ratio depending on the ore type, deposit age and Sm/Nd ratio. Together with other characteristics of the material in question, the Nd isotope ratio is a promising signature for nuclear forensics and suggests being indicative of the source material, the uranium ore. Copyright © 2014 The Authors. Published by Elsevier B.V. All rights reserved.

Exploration for uranium deposits in the Spring Creek Mesa area, Montrose County, Colorado

USGS Publications Warehouse

Roach, Carl Houston

1954-01-01

4. The “ore-bearing sandstone” in the vicinity of relatively unoxidized ore deposits commonly contains sparse to abundant disseminated pyrite. In the vicinity of oxidized deposits it commonly contains abundant limonite spots and widespread limonite staining.

SEPARATION OF TECHNETIUM FROM AQUEOUS SOLUTIONS BY COPRECIPITATION WITH MAGNETITE

DOEpatents

Rimshaw, S.J.

1961-10-24

A method of separating technetium in the 4+ oxidation state from an aqueous basic solution containing products of uranium fission is described. The method consists of contacting the solution with finely divided magnetite and recovering a technetium-bearing precipitate. (AEC)

Humic Acid Isolations from Lignite by Ion Exchange Method

NASA Astrophysics Data System (ADS)

Kurniati, E.; Muljani, S.; Virgani, D. G.; Neno, B. P.

2018-01-01

The humic liquid is produced from lignite extraction using alkali solution. Conventional humic acid is obtained by acidifying a humic solution using HCl. The purpose of this research is the formation of solid humic acid from lignite by ion exchange method using cation resin. The results showed that the addition of cation resin was able to reduce the pH from 14 to pH 2 as well as the addition of acid (HCl), indicating the exchange of Na + ions with H + ions. The reduction of pH in the humic solution is influenced by the concentration of sodium ions in the humic solution, the weight of the cation resin, and the ion exchange time. The IR spectra results are in good agreement for humic acid from lignite characterization.

A preliminary report on the geology of the Dennison-Bunn uranium claim, Sandoval County, New Mexico

USGS Publications Warehouse

Ridgley, Jennie L.

1978-01-01

Uranium at the Dennison-Bunn claim, south of Cuba, N. Mex., along the east margin of the San Juan Basin, occurs in unoxidized gray, fluvial channel sandstone of the Westwater Canyon Member of the Upper Jurassic Morrison Formation. The uranium-bearing sandstone is bounded on the north and south by a variable zone of buff and orange sandstone. Within the mineralized zone, the uranium has been remobilized and reconcentrated along the margins of numerous smaller tongues of oxidized rock in a configuration similar to that found in roll-type uranium deposits. In cross section, these small-scale features are zoned; they have an inner, pale orange, oxidized core, a mineralized redox rim cemented with hematite(?), and an outer-shell of -gray, slightly to moderately mineralized rock. The uranium content in the mineralized rock ranges from 0.001 to 0.07 percent U3O8. The uranium, at this locality, is believed to have originated within the Westwater Canyon Member or to have been derived from the overlying Brushy Basin Member. Based on observed outcrop relations, two hypotheses are proposed for explaining the origin of the occurrence. Briefly these hypotheses are: (1) the mineralized zone represents the remnant of an original roll-type uranium deposit, formed during early Eocene time, which has undergone subsequent oxidation with remobilization and redeposition of uranium around the margins of smaller tongues of oxidized rock; and (2) the mineralized zone represents the remnant of an original tabular deposit which has undergone subsequent oxidation with remobilization and redeposition of uranium around the margins of smaller tongues of oxidized rock.

Geologic sources and concentrations of selenium in the West-Central Denver Basin, including the Toll Gate Creek watershed, Aurora, Colorado, 2003-2007

USGS Publications Warehouse

Paschke, Suzanne S.; Walton-Day, Katherine; Beck, Jennifer A.; Webbers, Ank; Dupree, Jean A.

2014-01-01

Toll Gate Creek, in the west-central part of the Denver Basin, is a perennial stream in which concentrations of dissolved selenium have consistently exceeded the Colorado aquatic-life standard of 4.6 micrograms per liter. Recent studies of selenium in Toll Gate Creek identified the Denver lignite zone of the non-marine Cretaceous to Tertiary-aged (Paleocene) Denver Formation underlying the watershed as the geologic source of dissolved selenium to shallow ground-water and surface water. Previous work led to this study by the U.S. Geological Survey, in cooperation with the City of Aurora Utilities Department, which investigated geologic sources of selenium and selenium concentrations in the watershed. This report documents the occurrence of selenium-bearing rocks and groundwater within the Cretaceous- to Tertiary-aged Denver Formation in the west-central part of the Denver Basin, including the Toll Gate Creek watershed. The report presents background information on geochemical processes controlling selenium concentrations in the aquatic environment and possible geologic sources of selenium; the hydrogeologic setting of the watershed; selenium results from groundwater-sampling programs; and chemical analyses of solids samples as evidence that weathering of the Denver Formation is a geologic source of selenium to groundwater and surface water in the west-central part of the Denver Basin, including Toll Gate Creek. Analyses of water samples collected from 61 water-table wells in 2003 and from 19 water-table wells in 2007 indicate dissolved selenium concentrations in groundwater in the west-central Denver Basin frequently exceeded the Colorado aquatic-life standard and in some locations exceeded the primary drinking-water standard of 50 micrograms per liter. The greatest selenium concentrations were associated with oxidized groundwater samples from wells completed in bedrock materials. Selenium analysis of geologic core samples indicates that total selenium concentrations were greatest in samples containing indications of reducing conditions and organic matter (dark gray to black claystones and lignite horizons). The Toll Gate Creek watershed is situated in a unique hydrogeologic setting in the west-central part of the Denver Basin such that weathering of Cretaceous- to Tertiary-aged, non-marine, selenium-bearing rocks releases selenium to groundwater and surface water under present-day semi-arid environmental conditions. The Denver Formation contains several known and suspected geologic sources of selenium including: (1) lignite deposits; (2) tonstein partings; (3) organic-rich bentonite claystones; (4) salts formed as secondary weathering products; and possibly (5) the Cretaceous-Tertiary boundary. Organically complexed selenium and/or selenium-bearing pyrite in the enclosing claystones are likely the primary mineral sources of selenium in the Denver Formation, and correlations between concentration of dissolved selenium and dissolved organic carbon in groundwater indicate weathering and dissolution of organically complexed selenium from organic-rich claystone is a primary process mobilizing selenium. Secondary salts accumulated along fractures and bedding planes in the weathered zone are another potential geologic source of selenium, although their composition was not specifically addressed by the solids analyses. Results from this and previous work indicate that shallow groundwater and streams similarly positioned over Denver Formation claystone units at other locations in the Denver Basin also may contain concentrations of dissolved selenium greater than the Colorado aquatic-life standard or the drinking- water standard.

Study on the coal mixing ratio optimization for a power plant

NASA Astrophysics Data System (ADS)

Jin, Y. A.; Cheng, J. W.; Bai, Q.; Li, W. B.

2017-12-01

For coal-fired power plants, the application of blended coal combustion has been a great issue due to the shortage and rising prices of high-rank coal. This paper describes the optimization of blending methods between Xing'an lignite coal, Shaltala lignite coal, Ura lignite coal, and Inner Mongolia bituminous coal. The multi-objective decision-making method based on fuzzy mathematics was used to determine the optimal blending ratio to improve the power plant coal-fired economy.

Environmental Assessment: Construct Airfield Lighting Vault and Demolish Building 531 at Grand Forks Air Force Base

DTIC Science & Technology

2007-08-01

The backfill material shall be free of bentonite, trash, frozen or organic material including lignites, humus , sod, grass, roots or other...organic material including lignites, humus , sod, grass, roots or other vegetation. The backfill material shall not be of a size greater than 3 inches, may...lignites, humus , sod, grass, roots or other vegetation. The backfill material shall not be of a size greater than 3 inches, may not contain more than 12

Preliminary geologic investigation of the West Glendive lignite deposits, Dawson County, Montana

USGS Publications Warehouse

Banet, Arthur C.

1979-01-01

Four major lignite beds, all in the Fort Union Formation (Paleocene), occur in the West Glendive area, Dawson County, Montana. The Newton Ranch and Poverty Flats beds are in the Lebo Member and the Peuse and Kolberg Ranch beds are in the Tongue River Member. Correlation of the lignite beds across the area shows that the Peuse bed is the thickest and most extensive. Field mapping and drill-hole data indicate that folding and faulting are more common than previously reported.

Reactivity of iron-rich phyllosilicates with uranium and chromium through redox transition zones

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

Burgos, William D.

This project performed thermodynamic, kinetic, and mineral structural studies on the reactivity of phyllosilicate Fe(II/III) with metal-reducing bacteria, and with two important poly-valent DOE contaminants (chromium and uranium) that show high mobility in their oxidized state. We focused on Fe-bearing phyllosilicates because these are important components of the reactive, fines fraction of Hanford, Oak Ridge, and Idaho National Laboratory sediments. Iron-bearing phyllosilicates strongly influence the redox state and mobility of Cr and U because of their limited hydraulic conductivity, high specific surface area, and redox reactivity. This was a collaborative project between Penn State (W.D. Burgos – PI), Miami Universitymore » (H. Dong – Co-PI), and Argonne National Laboratory (K. Kemner and M. Boyanov – Co-PIs). Penn State and Miami University were funded together but separately from ANL. This report summarizes research findings and publications produced by Penn State and Miami University.« less

Oxidation kinetics of hydride-bearing uranium metal corrosion products

NASA Astrophysics Data System (ADS)

Totemeier, Terry C.; Pahl, Robert G.; Frank, Steven M.

The oxidation behavior of hydride-bearing uranium metal corrosion products from Zero Power Physics Reactor (ZPPR) fuel plates was studied using thermo-gravimetric analysis (TGA) in environments of Ar-4%O 2, Ar-9%O 2, and Ar-20%O 2. Ignition of corrosion product samples from two moderately corroded plates was observed between 125°C and 150°C in all environments. The rate of oxidation above the ignition temperature was found to be dependent only on the net flow rate of oxygen in the reacting gas. Due to the higher net oxygen flow rate, burning rates increased with increasing oxygen concentration. Oxidation rates below the ignition temperature were much slower and decreased with increasing test time. The hydride contents of the TGA samples from the two moderately corroded plates, determined from the total weight gain achieved during burning, were 47-61 wt% and 29-39 wt%. Samples from a lightly corroded plate were not reactive; X-ray diffraction (XRD) confirmed that they contained little hydride.

Determination of optimal environmental policy for reclamation of land unearthed in lignite mines - Strategy and tactics

NASA Astrophysics Data System (ADS)

Batzias, Dimitris F.; Pollalis, Yannis A.

2012-12-01

In this paper, optimal environmental policy for reclamation of land unearthed in lignite mines is defined as a strategic target. The tactics concerning the achievement of this target, includes estimation of optimal time lag between each lignite site (which is a segment of the whole lignite field) complete exploitation and its reclamation. Subsidizing of reclamation has been determined as a function of this time lag and relevant implementation is presented for parameter values valid for the Greek economy. We proved that the methodology we have developed gives reasonable quantitative results within the norms imposed by legislation. Moreover, the interconnection between strategy and tactics becomes evident, since the former causes the latter by deduction and the latter revises the former by induction in the time course of land reclamation.

Assessment of potential migration of radionuclides and trace elements from the White Mesa uranium mill to the Ute Mountain Ute Reservation and surrounding areas, southeastern Utah

USGS Publications Warehouse

Naftz, David L.; Ranalli, Anthony J.; Rowland, Ryan C.; Marston, Thomas M.

2011-01-01

In 2007, the Ute Mountain Ute Tribe requested that the U.S. Environmental Protection Agency and U.S. Geological Survey conduct an independent evaluation of potential offsite migration of radionuclides and selected trace elements associated with the ore storage and milling process at an active uranium mill site near White Mesa, Utah. Specific objectives of this study were (1) to determine recharge sources and residence times of groundwater surrounding the mill site, (2) to determine the current concentrations of uranium and associated trace elements in groundwater surrounding the mill site, (3) to differentiate natural and anthropogenic contaminant sources to groundwater resources surrounding the mill site, (4) to assess the solubility and potential for offsite transport of uranium-bearing minerals in groundwater surrounding the mill site, and (5) to use stream sediment and plant material samples from areas surrounding the mill site to identify potential areas of offsite contamination and likely contaminant sources.

Formation of unprecedented actinidecarbon triple bonds in uranium methylidyne molecules

PubMed Central

Lyon, Jonathan T.; Hu, Han-Shi; Andrews, Lester; Li, Jun

2007-01-01

Chemistry of the actinide elements represents a challenging yet vital scientific frontier. Development of actinide chemistry requires fundamental understanding of the relative roles of actinide valence-region orbitals and the nature of their chemical bonding. We report here an experimental and theoretical investigation of the uranium methylidyne molecules X3UCH (X = F, Cl, Br), F2ClUCH, and F3UCF formed through reactions of laser-ablated uranium atoms and trihalomethanes or carbon tetrafluoride in excess argon. By using matrix infrared spectroscopy and relativistic quantum chemistry calculations, we have shown that these actinide complexes possess relatively strong UC triple bonds between the U 6d-5f hybrid orbitals and carbon 2s-2p orbitals. Electron-withdrawing ligands are critical in stabilizing the U(VI) oxidation state and sustaining the formation of uranium multiple bonds. These unique UC-bearing molecules are examples of the long-sought actinide-alkylidynes. This discovery opens the door to the rational synthesis of triple-bonded actinidecarbon compounds. PMID:18024591

PURIFICATION PROCESS

DOEpatents

Wibbles, H.L.; Miller, E.I.

1958-01-14

This patent deals with the separation of uranium from molybdenum compounds, and in particular with their separation from ether solutions containing the molybdenum in the form of acids, such as silicomolybdic and phosphomolybdic acids. After the nitric acid leach of pitchblende, the molybdenum values present in the ore are found in the leach solution in the form of complex acids. The uranium bearing solution may be purified of this molybdenum content by comtacting it with activated charcoal. The purification is improved when the acidity of the solution is low ad agitation is also beneficial. The molybdenum may subsequently be recovered from the charcosl ad the charcoal reused.

A possible link between Balkan endemic nephropathy and the leaching of toxic organic compounds from Pliocene lignite by groundwater: Preliminary investigation

USGS Publications Warehouse

Orem, W.H.; Feder, G.L.; Finkelman, R.B.

1999-01-01

Balkan endemic nephropathy (BEN) is a fatal kidney disease that is known to occur only in clusters of villages in alluvial valleys of tributaries of the Danube River in Bulgaria, Romania, Yugoslavia, Bosnia, and Croatia. The confinement of this disease to a specific geographic area has led to speculation that an environmental factor may be involved in the etiology of BEN. Numerous environmental factors have been suggested as causative agents for producing BEN, including toxic metals in drinking water, metal deficiency in soils of BEN areas, and environmental mycotoxins to name a few. These hypotheses have either been disproved or have failed to conclusively demonstrate a connection to the etiology of BEN, or the clustering of BEN villages. In previous work, we observed a distinct geographic relationship between the distribution of Pliocene lignites in the Balkans and BEN villages. We hypothesized that the long-term consumption of well water containing toxic organic compounds derived from the leaching of nearby Pliocene lignites by groundwater was a primary factor in the etiology of BEN. In our current work, chemical analysis using 13C nuclear magnetic resonance (13CNMR) spectroscopy indicated a high degree of organic functionality in Pliocene lignite from the Balkans, and suggested that groundwater can readily leach organic matter from these coal beds. Semi-quantitative gas chromatography/mass spectroscopy analysis of solvent extracts of groundwater from shallow wells in BEN villages indicated the presence of potentially toxic aromatic compounds, such as napthalene, fluorene, phenanthrene, and pyrene at concentrations in the ppb range. Laboratory leaching of Balkan Pliocene lignites with distilled water yielded soluble organic matter (> 500 MW) containing large amounts of aromatic structures similar to the simple/discrete aromatic compounds detected in well water from BEN villages. These preliminary results are permissive of our hypothesis and suggest that further work on the possible relationship between the etiology of BEN and toxic aromatic substances leached from Pliocene lignites in well water is warranted.A distinct geographic relationship between the distribution of Pliocene lignites in the Balkans and villages where Balkan endemic nephropathy (BEN) occurs has been observed, indicating a possible link between BEN and the long-term consumption of well water containing toxic organic compounds derived from the leaching of nearby Pliocene lignites. Preliminary investigations by NMR spectroscopy, gas chromatography/mass spectroscopy and leaching experiments show a high degree of organic functionality in the Pliocene lignites, high-leachability by groundwater of organic matter from these beds, and the presence of toxic aromatic compounds.

Handbook on surficial uranium deposits. Chapter 3. World distribution relative to climate and physical setting

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

Carlisle, D

1983-01-01

This chapter discusses regional controls which affect the world distribution of surficial chemogenic uranium deposits. The most important of these are (1) climate, (2) geomorphology, including physiographic and climatic stability, and (3) provenance, i.e., the weathering terrain from which uranium and associated substances are derived. The three economically important environments are the calcrete environment, simple evaporative environments and paludal environments. Of these three categories, the calcrete uranium environment is probably the most uniquely constrained in terms of regional climate, geomorphic setting, provenance (vanadium as well as uranium) and especially the need for long term stability of both climate and physiography.more » Purely evaporative deposits, though subject to some of the same kinds of constraints, can also reflect local circumstances and a wider range of climates, physiographic settings, and source terrains. The third category encompassing bogs, marshes and organic-rich playas can form under an even wider range of climates and settings provided only that organic materials accumulate in abundance and are contacted by uranium-bearing waters. For all of these reasons and also because of the great economic importance of the calcrete environment as well as its relative novelty and complexity the discussion in this chapter is focused on calcrete, dolocrete and gypcrete uranium deposits. Objective data are reviewed first follwed by inferences and suggestions. 13 figures.« less

Wind Transport of Radionuclide- Bearing Dust, Peña Blanca, Chihuahua, Mexico

NASA Astrophysics Data System (ADS)

Velarde, R.; Goodell, P. C.; Gill, T. E.; Arimoto, R.

2007-05-01

This investigation evaluates radionuclide fractionation during wind erosion of high-grade uranium ore storage piles at Peña Blanca (50km north of Chihuahua City), Chihuahua, Mexico. The aridity of the local environment promotes dust resuspension by high winds. Although active operations ceased in 1983, the Peña Blanca mining district is one of Mexico`s most important uranium ore reserves. The study site contains piles of high grade ore, left loose on the surface, and separated by the specific deposits from which they were derived (Margaritas, Nopal I, and Puerto I). Similar locations do not exist in the United States, since uranium mining sites in the USA have been reclaimed. The Peña Blanca site serves as an analog for the Yucca Mountain project. Dust deposition is collected at Peña Blanca with BSNE sediment catchers (Fryrear, 1986) and marble dust traps (Reheis, 1999). These devices capture windblown sediment; subsequently, the sample data will help quantify potentially radioactive short term field sediment loss from the repository surface and determine sediment flux. Aerosols and surface materials will be analyzed and radioactivity levels established utilizing techniques such as gamma spectroscopy. As a result, we will be able to estimate how much radionuclide contaminated dust is being transported or attached geochemically to fine grain soils or minerals (e.g., clays or iron oxides). The high-grade uranium-bearing material is at secular equilibrium, thus the entire decay series is present. Of resulting interest is not only the aeolian transport of uranium, but also of the other daughter products. These studies will improve our understanding of geochemical cycling of radionuclides with respect to sources, transport, and deposition. The results may also have important implications for the geosciences and homeland security, and potential applications to public health. Funding for this project is provided in part via a NSF grant to Arimoto.

Map showing radon potential of rocks and soils in Fairfax County, Virginia

USGS Publications Warehouse

Otton, James K.; Schumann, R. Randall; Owen, Douglass E.; Thurman, Nelson; Duval, Joseph S.

1988-01-01

Since 1984, indoor radon has gained national attention as a significant health hazard in the United States. Radon is a colorless, odorless, radioactive gas derived from uranium by radioactive decay. The U.S. Environmental Protection Agency (EPA) now projects that 5,000 to 20,000 lung-cancer deaths per year may be attributed to the long-term exposure to indoor radon and its radioactive decay products. Indoor radon has been previously recognized as a health hazard associated with uranium-bearing mill tailings or building materials, but it was not until December 1984 that some natural soils and rocks were found to be sources of indoor radon at levels comparable to those in uranium mines. It is now suspected that elevated indoor radon levels are far more widespread than initially though. The EPA considers 4 picoCuries of radon per liter of air (pCi/L) as the level (in a year-round measurement) at which actions ought to be taken to lower the concentration of indoor radon. All soils and rocks contain measurable amounts of uranium, which generate measurable amounts of radon. Certain soils and rocks, however, have a greater potential to cause indoor radon problems than others because (1) they have a higher uranium content and thus can generate higher levels of radon in soil gas (gas that occupies the pores of the soil), and (2) the permeability of the sol or rack is sufficiently high that radon-bearing soil gas can flow freely and move indoors through the foundation of the structure. This study was designed to demonstrate the correlation between the geologic environment and indoor radon levels and to demonstrate a method of assessment that could be used by other informed workers in areas of their interest. A parallel study by Gundersen and others (1988) of the radon potential of rocks and soils in Montgomery County, Md., used somewhat different methods of assessment because the data available for and assessment of Montgomery County differed.

Naturally Occurring Radionuclides of Ash Produced by Coal Combustion. The Case of the Kardia Mine in Northern Greece

NASA Astrophysics Data System (ADS)

Fotakis, M.; Tsikritzis, L.; Tzimkas, N.; Kolovos, N.; Tsikritzi, R.

2008-08-01

West Macedonia Lignite Center (WMLC), located in Northwest Greece, releases into the atmosphere about 21,400 tons/year of fly ash through the stacks of four coal fired plants. The lignite ash contains naturally occurring radionuclides, which are deposited on the WMLC basin. This work investigates the natural radioactivity of twenty six ash samples, laboratory produced from combustion of lignite, which was sampled perpendicularly to the benches of the Kardia mine. The concentrations of radionuclides 40K, 235U, 238U, 226Ra, 228Ra and 232Th, were measured spectroscopically and found round one order of magnitude as high as those of lignite. Subsequently the Radionuclide Partitioning Coefficients of radionuclides were calculated and it was found that they are higher for 232Th, 228Ra and 40K, because the latter have closer affinity with the inorganic matrix of lignite. During combustion up to one third of the naturally occurring radioisotopes escape from the solid phase into the flue gases. With comparison to relative global data, the investigated ash has been found to have relatively high radioactivity, but the emissions of the WMLC radionuclides contribute only 0.03% to the mean annual absorbed dose.

Environmental geology of the Wilcox Group Lignite Belt, east Texas

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

Henry, C.D.; Basciano, J.M.

This report provides a data base for decisions about lignite mining and reclamation in the Wilcox Group of East Texas. A set of environmental geologic maps, which accompanies this report, depicts the character of the land that will be affected by mining. The environmental geologic maps of the East Texas lignite belt provide an accurate inventory of land resources. The maps identify areas where mining is most likely to occur, areas of critical natural resources that could be affected by mining, such as aquifer recharge areas, and areas of natural hazards, such as floodplains. Principal areas of both active andmore » planned surface mining are also located. The seven environmental geologic maps cover the outcrop area of the Wilcox Group, the major lignite host, and adjacent geologic units from Bastrop County to Texarkana. This report begins with a discussion of various physical aspects of the lignite belt, including geology, hydrology, soils, climate, and land use, to aid in understanding the maps. The criteria and methodology used to delineate the environmental geologic units are discussed. Varied applications of the environmental geologic maps are considered. 23 references, 9 figures, 3 tables.« less

Leaching behavior of rare earth elements in Fort Union lignite coals of North America

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

Laudal, Daniel A.; Benson, Steven A.; Addleman, Raymond Shane

Rare earth elements are crucial materials in an incredible array of consumer goods, energy system components and military defense applications. However, the global production and entire value chain for rare earth elements is dominated by China, with the U.S. currently 100% import reliant for these critical materials. Traditional mineral ores including those previously mined in the U.S., however, have several challenges. Chief among these is that the content of the most critical and valuable of the rare earths are deficient, making mining uneconomical. Further, the supply of these most critical rare earths is nearly 100% produced in China from amore » single resource that is only projected to last another 10 to 20 years. The U.S. currently considers the rare earths market an issue of national security. It is imperative that alternative domestic sources of rare earths be identified and methods developed to produce them. Recently, coal and coal byproducts have been identified as one of these promising alternative resources. This paper details the results of a study on characterization of North Dakota lignite and lignite-related feedstocks as an assessment of their feasibility for rare earth element recovery. The abundance, distribution and modes of occurrence of the rare earth elements in the samples collected were determined in this initial study to inform the selection of appropriate extraction and concentration methods to recover the rare earth elements. Materials investigated include the lignite coals, clay-rich sediments associated with the coal seams, and materials associated with a lignite beneficiation system and power plant. The results show that high rare earth element levels exist both in lignite coals and associated sediments. The form of the rare earth elements in the clay materials is primarily as ultra-fine mineral grains. In the lignite coals, approximately 80-95% of the rare earths content is organically associated, primarily as coordination complexes.« less

Paleocene-eocene lignite beds of southwest Alabama: Parasequence beds in highstand systems tracts

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

Mancini, E.A.; Tew, B.H.; Carroll, R.E.

1993-09-01

In southwest Alabama, lignite beds are present in at least four stratigraphic intervals that span approximately 8 m.y. of geologic time. Lignite is found in the Paleocene Oak Hill Member and Coal Bluff Member of the Naheola Formation of the Midway Group and the Paleocene Tuscahoma Sand and the Eocene Hatchetigbee Formation of the Wilcox Group. Lignite beds range in thickness from 0.5 to 11 ft and consist of 32-53% moisture, 13-39% volatile matter, 4-36% fixed carbon, and 5-51% ash. These Paleocene and Eocene lignite beds occur as parasequence deposits in highstand systems tracts of four distinct third-order depositional sequences.more » The lignite beds are interpreted as strata within highstand systems tract parasequences that occur in mud-dominated regressive intervals. Lignite beds were deposited in coastal marsh and low-lying swamp environments as part of deltaic systems that prograded into southwestern Alabama from the west. As sediment was progressively delivered into the basin from these deltas, the effects of relative sea level rise during an individual cycle were overwhelmed, producing a net loss of accommodation and concomitant overall basinward progradation of the shoreline (regression). Small-scale fluctuations in water depth resulting from the interaction of eustasy, sediment yield, and subsidence led to cyclical flooding of the low-lying coastal marshes and swamps followed by periods of progradational and regression. Highstand systems tract deposition within a particular depositional sequence culminated with a relative sea level fall that resulted in a lowering of base level and an abrupt basinward shift in coastal onlap. Following sea level fall and the subsequent accumulation of the lowstand deposits, significant relative sea level rise resulted in the marine inundation of the area previously occupied by coastal marshes and swamps and deposition of the transgressive systems tract of the overlying sequence.« less

Natural desulfurization in coal-fired units using Greek lignite.

PubMed

Konidaris, Dimitrios N

2010-10-01

This paper analyzes the natural desulfurization process taking place in coal-fired units using Greek lignite. The dry scrubbing capability of Greek lignite appears to be extremely high under special conditions, which can make it possible for the units to operate within the legislative limits of sulfur dioxide (SO2) emissions. According to this study on several lignite-fired power stations in northern Greece, it was found that sulfur oxide emissions depend on coal rank, sulfur content, and calorific value. On the other hand, SO2 emission is inversely proportional to the parameter gammaCO2(max), which is equal to the maximum carbon dioxide (CO2) content by volume of dry flue gas under stoichiometric combustion. The desulfurization efficiency is positively correlated to the molar ratio of decomposed calcium carbonate to sulfur and negatively correlated to the free calcium oxide content of fly ash.

Drill-hole data, drill-site geology, and geochemical data from the study of Precambrian uraniferous conglomerates of the Medicine Bow Mountains and Sierra Madre of southeastern Wyoming

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

Karlstrom, K.E.; Houston, R.S.; Schmidt, T.G.

1981-02-01

This volume is presented as a companion to Volume 1: The Geology and Uranium Potential of Precambrian Conglomerates in the Medicine Bow Mountains and Sierra Madre of Southeastern Wyoming; and to Volume 3: Uranium Assessment for Precambrian Pebble Conglomerates in Southeastern Wyoming. Volume 1 summarized the geologic setting and geologic and geochemical characteristics of uranium-bearing conglomerates in Precambrian metasedimentary rocks of southeastern Wyoming. Volume 3 is a geostatistical resource estimate of U and Th in quartz-pebble conglomerates. This volume contains supporting geochemical data, lithologic logs from 48 drill holes in Precambrian rocks of the Medicine Bow Mountains and Sierra Madre,more » and drill site geologic maps and cross-sections from most of the holes.« less

Aerial radiometric and magnetic reconnaissance survey of the Eagle--Dillingham area, Alaska, Mt. Hayes Quadrangle

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

Not Available

1978-06-01

The results of a high-sensitivity aerial gamma-ray spectrometer and magnetometer survey of the Mt. Hayes Quadrangle, Alaska, are presented. Instrumentation and methods are described in Volume 1 of this final report. Statistical and geological analysis of the radiometric data revealed two uranium anomalies worthy of field checking as possible prospects. One is located near Mesozoic granite, which is believed to have the best potential for future economic uranium deposits. Another uranium anomaly is associated with Paleozoic-Precambrian rocks and may be caused by augen gneiss or possibly granitic intrusives. Two weakly uraniferous provinces merit study: one in the northwest, which maymore » be related to the Tertiary-Cretaceous coal-bearing unit, and a second in the northeast, which may be related to Mesozoic granites.« less

Microbial reduction of U(VI) under alkaline conditions: implications for radioactive waste geodisposal.

PubMed

Williamson, Adam J; Morris, Katherine; Law, Gareth T W; Rizoulis, Athanasios; Charnock, John M; Lloyd, Jonathan R

2014-11-18

Although there is consensus that microorganisms significantly influence uranium speciation and mobility in the subsurface under circumneutral conditions, microbiologically mediated U(VI) redox cycling under alkaline conditions relevant to the geological disposal of cementitious intermediate level radioactive waste, remains unexplored. Here, we describe microcosm experiments that investigate the biogeochemical fate of U(VI) at pH 10-10.5, using sediments from a legacy lime working site, stimulated with an added electron donor, and incubated in the presence and absence of added Fe(III) as ferrihydrite. In systems without added Fe(III), partial U(VI) reduction occurred, forming a U(IV)-bearing non-uraninite phase which underwent reoxidation in the presence of air (O2) and to some extent nitrate. By contrast, in the presence of added Fe(III), U(VI) was first removed from solution by sorption to the Fe(III) mineral, followed by bioreduction and (bio)magnetite formation coupled to formation of a complex U(IV)-bearing phase with uraninite present, which also underwent air (O2) and partial nitrate reoxidation. 16S rRNA gene pyrosequencing showed that Gram-positive bacteria affiliated with the Firmicutes and Bacteroidetes dominated in the post-reduction sediments. These data provide the first insights into uranium biogeochemistry at high pH and have significant implications for the long-term fate of uranium in geological disposal in both engineered barrier systems and the alkaline, chemically disturbed geosphere.

Petrography and geochemistry of selected lignite beds in the Gibbons Creek mine (Manning Formation, Jackson Group, Paleocene) of east-central Texas

USGS Publications Warehouse

Warwick, Peter D.; Crowley, Sharon S.; Ruppert, Leslie F.; Pontolillo, James

1997-01-01

This study examined the petrographic and geochemical characteristics of two lignite beds (3500 and 4500 beds, Manning Formation, Jackson Group, Eocene) that are mined at the Gibbons Creek mine in east-central Texas. The purpose of the study was to identify the relations among sample ash yield, coal petrography, and trace-element concentrations in lignite and adjoining rock layers of the Gibbons Creek mine. Particular interest was given to the distribution of 12 environmentally sensitive trace elements (As, Be, Cd, Cr, Co, Hg, Mn, Ni, Pb, Sb, Se, and U) that have been identified as potentially hazardous air pollutants (HAPs) in the United States Clean Air Act Amendments of 1990. Eleven lignite, floor, and rock parting samples were collected from incremental channel samples of the 3500 and 4500 beds that were exposed in a highwall of pit A3 at the Gibbons Creek mine. Short proximate and ultimate and forms of sulfur analyses were performed on all lignite samples, and lignite and rock samples were analyzed for 60 major, minor and trace elements. Representative splits of all lignite samples were ground and cast into pellets, and polished for petrographic analyses in blue-light fluorescence and reflected white light to determine liptinite, inertinite, and huminite maceral group percentages. The following observations summarize our results and conclusions about the geochemistry, petrography, and sedimentology of the 3500 and 4500 beds of the Gibbons Creek lignite deposit: (1) Weighted average dry (db) ash yield for the two beds is 29.7%, average total sulfur content is 2.6%, and average calorific value is 7832 Btu (18.22 MJ/kg). Ash yields are greatest in the lower bench (59.33% db) of the 3500 bed and in the upper bench of the 4500 bed (74.61% db). (2) For lignite samples (on a whole-coal basis), the distributions of two of the HAPs (Pb and Sb) are positively related to ash yield, probably indicating an inorganic affinity for these elements. By using cluster analysis we found that Be and Cd were poorly associated with ash yield, indicating a possible organic affinity, and that Ni, Se, Hg, U, and Pb cluster with most of the rare-earth elements. (3) The dominance of the crypto-eugelinite maceral subgroup over the crypto-humotelinite subgroup suggests that all Gibbons Creek lignites were subjected to peat-forming conditions (either biogenic or chemical) conducive to the degradation of wood cellular material into matrix gels, or that original plant material was not very woody and was prone to formation of matrix gels. The latter idea is supported by pollen studies of Gibbons Creek lignite beds; results indicate that the peat was derived in part from marsh plants low in wood tissue. (4) The occurrence of siliceous sponge spicules in the lower benches of the 3500 bed suggests the original peat in this part of the bed was deposited in standing, fresh water. (5) The petrographic data indicate that the upper sample interval of the 3500 bed contains more inertinite (3%) than the other samples studied. Increases in inertinite content in the upper part of the 3500 bed may have been associated with alteration of the peat by acids derived from the volcanic ash or could have been caused by fire, oxidation and drying, or biologic alteration of the peat in the paleo-mire.

Germanium and uranium in coalified wood bom upper Devonian black shale

USGS Publications Warehouse

Breger, I.A.; Schopf, J.M.

1955-01-01

Microscopic study of black, vitreous, carbonaceous material occurring in the Chattanooga shale in Tennessee and in the Cleveland member of the Ohio shale in Ohio has revealed coalified woody plant tissue. Some samples have shown sufficient detail to be identified with the genus Cauixylon. Similar material has been reported in the literature as "bituminous" or "asphaltic" stringers. Spectrographic analyses of the ash from the coalified wood have shown unusually high percentages of germanium, uranium, vanadium, and nickel. The inverse relationship between uranium and germanium in the ash and the ash content of various samples shows an association of these elements with the organic constituents of the coal. On the basis of geochemical considerations, it seems most probable that the wood or coalified wood was germanium-bearing at the time logs or woody fragmenta were floated into the basins of deposition of the Chattanooga shale and the Cleveland member of the Ohio shale. Once within the marine environment, the material probably absorbed uranium with the formation of organo-uranium compounds such as exist in coals. It is suggested that a more systematic search for germaniferous coals in the vicinity of the Chattanooga shale and the Cleveland member of the Ohio shale might be rewarding. ?? 1955.

Geohydrologic reconnaissance of the Avoca lignite deposit area near Williston, northwestern North Dakota

USGS Publications Warehouse

Horak, W.F.; Crosby, O.A.

1985-01-01

The Avoca lignite deposit in the Sentinel Butte Member of the Fort Union Formation consists of four potentially strippable lignite beds. Average bed thicknesses, in descending order, are 5, 5, 9, and 8 .feet. In the area between Stony Creek and Crazy Man Coulee, the lignite beds are unsaturated, and between Stony Creek and Little Muddy River, only the two lowest beds are saturated. Natural discharge to outcrops in the stream valleys results in low potentiometric levels in the lignite beds.Aquifers in sandstone beds in the Fox Hills Sandstone and the Hell Creek Formation probably would yield as much as 50 gallons per minute of sodium bicarbonate type water. Dissolved-solids concentrations range from 800 to 2,000 milligrams per liter. The aquifers are from 1,100 to 1,800 feet below land surface. Sandstone beds in the Ludlow and Cannonball Members of the Fort Union Formation probably could yield several gallons per minute of sodium bicarbonate water with dissolved-solids concentrations ranging from 800 to 2,000 milligrams per liter. Aquifers in the Ludlow and Cannonball Members lie between 700 and 1,300 feet below land surface. Individual sand beds in the Tongue River and Sentinel Butte Members of the Fort Union Formation are the shallowest aquifers encountered below the minable lignite beds. Properly constructed wells completed in these sand beds could yield as much as 40 gallons per minute. The water generally is a sodium bicarbonate type with dissolved-solids concentrations ranging from about 500 to 4,200 milligrams per liter. Alluvium and glacial-drift deposits constitute the Little Muddy aquifer bordering the lignite deposit on the west and south. The aquifer could yield as much as 1,200 gallons per minute of sodium bicarbonate type water with dissolved-solids concentrations ranging from 975 to 1, 730 milligrams per liter.Little Muddy Creek and Stony Creek have significant base flow. The flow is contributed partly by discharge from the lignite. Quality of water is least mineralized at high stream flows. Mining would not severely affect ground-water levels because potentiometric levels already are low. Chemically enriched leachate water from the spoils could percolate to the saturated zone and eventually reach the streams as base flow or recharge the glaciofluvial aquifers.

Secondary Structures in a Freeze-Dried Lignite Humic Acid Fraction Caused by Hydrogen-Bonding of Acidic Protons with Aromatic Rings.

PubMed

Cao, Xiaoyan; Drosos, Marios; Leenheer, Jerry A; Mao, Jingdong

2016-02-16

A lignite humic acid (HA) was separated from inorganic and non-HA impurities (i.e., aluminosilicates, metals) and fractionated by a combination of dialysis and XAD-8 resin. Fractionation revealed a more homogeneous structure of lignite HA. New and more specific structural information on the main lignite HA fraction is obtained by solid-state nuclear magnetic resonance (NMR) spectroscopy. Quantitative (13)C multiple cross-polarization (multiCP) NMR indicated oxidized phenyl propane structures derived from lignin. MultiCP experiments, conducted on potassium HA salts titrated to pH 10 and pH 12, revealed shifts consistent with carboxylate and phenolate formation, but structural changes associated with enolate formation from aromatic beta keto acids were not detected. Two-dimensional (1)H-(13)C heteronuclear correlation (2D HETCOR) NMR indicated aryl-aliphatic ketones, aliphatic and aromatic carboxyl groups, phenol, and methoxy phenyl ethers. Acidic protons from carboxyl groups in both the lignite HA fraction and a synthetic HA-like polycondensate were found to be hydrogen-bonded with electron-rich aromatic rings. Our results coupled with published infrared spectra provide evidence for the preferential hydrogen bonding of acidic hydrogens with electron-rich aromatic rings rather than adjacent carbonyl groups. These hydrogen-bonding interactions likely result from stereochemical arrangements in primary structures and folding.

Carbonate and lignite cycles in the Ptolemais Basin: Orbital control and suborbital variability (Late Neogene, northern Greece)

NASA Astrophysics Data System (ADS)

Weber, M. E.; Tougiannidis, N.; Ricken, W.; Rolf, C.; Kleineder, M.; Bertram, N.; Antoniadis, P.

2009-04-01

We recently commenced a project to investigate deep drillings as well as outcrops in the Ptolemais Basin, northern Greece, for paleoenvironmental and paleoclimate change. Specific attention is paid to mining sites Achlada, Vevi, Vegora, Amynteon, North Field, South Field, and Lava. The sediment archive comprises Upper Miocene to Quaternary continental lake deposits (up to 800 m thick) with an extended Lower Pliocene section. The Upper Miocene sections are composed of diatomaceous mud and gray marls. Pliocene lake sediments commence with the Kyrio member (lignite/grey marl), followed by the Theodoxus member (beige marl/lignite), and the Notio member (marl with intercalated sand /lignite). The limnic deposits show striking rhythmic bedding of (mostly) carbonates and lignites, reflecting orbital-induced humidity and temperature changes in this small NW-SE elongated continental basin. First, we retrieved chronometric information by determining magnetic polarity changes on three sites as independent stratigraphic ground-truth in combination with palynological evidence and published data. Then we conducted a number of high-resolution (1 - 6 cm increment), non-destructive measurements to obtain paleoclimate proxies: photospectrometry (colors L, a, b), magnetic susceptibility, and natural gamma. Accordingly, we achieved a multi-proxy insight into paleoclimate and paleoenvironmental evolution at unprecedented temporal resolution (up to a few decades!) over long time series and at a number of key sites. Using the newly-developed ESALab software, we conducted spectral and evolutionary spectral analysis to evaluate the cyclo-stratigraphic development. As for orbital variability, spectral power is concentrated on precession, hemi-precession, and eccentricity, with only minor impact of orbital tilt. We used this information to increase the temporal resolution of our age models by tuning as many precession (insolation) maxima as possible to carbonate minima (lignite maxima), assuming that the lignite phase is associated with maximum temperature and humidity. The reason to apply the tuning was primarily to obtain a better temporal control on the cyclicity documented in the suborbital frequency band. These higher-frequency variations provide a significant contribution and visually resemble those that have been documented for the Greenland Ice Sheet during the last glacial cycle. Future goals of our work include the establishment of possible teleconnections to other parts of the global climate system. We would like to evaluate (i) how the aridification of the Messinian salinity crisis affected the Upper Miocene limnic record, (ii) why the lignite production was enhanced during the warm Lower Pliocene and how the link to the warm global climate might have been created, and (iii) whether the massive northern hemisphere glaciation during the Upper Pliocene might have contributed to the termination of lignite formation in the Ptolemais Basin.

Non-enzymatic U(VI) interactions with biogenic mackinawite

NASA Astrophysics Data System (ADS)

Veeramani, H.; Qafoku, N. P.; Kukkadapu, R. K.; Murayama, M.; Hochella, M. F.

2011-12-01

Reductive immobilization of hexavalent uranium [U(VI)] by stimulation of dissimilatory metal and/or sulfate reducing bacteria (DMRB or DSRB) has been extensively researched as a remediation strategy for subsurface U(VI) contamination. These bacteria derive energy by reducing oxidized metals as terminal electron acceptors, often utilizing organic substrates as electron donors. Thus, when evaluating the potential for in-situ uranium remediation in heterogeneous subsurface media, it is important to understand how the presence of alternative electron acceptors such as Fe(III) and sulfate affect U(VI) remediation and the long term behavior and reactivity of reduced uranium. Iron, an abundant subsurface element, represents a substantial sink for electrons from DMRB, and the reduction of Fe(III) leads to the formation of dissolved Fe(II) or to reactive biogenic Fe(II)- and mixed Fe(II)/Fe(III)- mineral phases. Consequently, abiotic U(VI) reduction by reactive forms of biogenic Fe(II) minerals could be a potentially important process for uranium immobilization. In our study, the DMRB Shewanella putrefaciens CN32 was used to synthesize a biogenic Fe(II)-bearing sulfide mineral: mackinawite, that has been characterized by XRD, SEM, HRTEM and Mössbauer spectroscopy. Batch experiments involving treated biogenic mackinawite and uranium (50:1 molar ratio) were carried out at room temperature under strict anoxic conditions. Following complete removal of uranium from solution, the biogenic mackinawite was analyzed by a suite of analytical techniques including XAS, HRTEM and Mössbauer spectroscopy to determine the speciation of uranium and investigate concomitant Fe(II)-phase transformation. Determining the speciation of uranium is critical to success of a remediation strategy. The present work elucidates non-enzymatic/abiotic molecular scale redox interactions between biogenic mackinawite and uranium.

Redox-Active vs Redox-Innocent: A Comparison of Uranium Complexes Containing Diamine Ligands.

PubMed

Pattenaude, Scott A; Mullane, Kimberly C; Schelter, Eric J; Ferrier, Maryline G; Stein, Benjamin W; Bone, Sharon E; Lezama Pacheco, Juan S; Kozimor, Stosh A; Fanwick, Phillip E; Zeller, Matthias; Bart, Suzanne C

2018-05-11

Uranium complexes ( Mes DAE) 2 U(THF) (1-DAE) and Cp 2 U( Mes DAE) (2-DAE) ( Mes DAE = [ArN-CH 2 CH 2 -NAr]; Ar = 2,4,6-trimethylphenyl (Mes)), bearing redox-innocent diamide ligands, have been synthesized and characterized for a full comparison with previously published, redox-active diimine complexes, ( Mes DAB Me ) 2 U(THF) (1-DAB) and Cp 2 U( Mes DAB Me ) (2-DAB) ( Mes DAB Me = [ArN═C(Me)C(Me)═NAr]; Ar = Mes). These redox-innocent analogues maintain an analogous steric environment to their redox-active ligand counterparts to facilitate a study aimed at determining the differing electronic behavior around the uranium center. Structural analysis by X-ray crystallography showed 1-DAE and 2-DAE have a structural environment very similar to 1-DAB and 2-DAB, respectively. The main difference occurs with coordination of the ene-backbone to the uranium center in the latter species. Electronic absorption spectroscopy reveals these new DAE complexes are nearly identical to each other. X-ray absorption spectroscopy suggests all four species contain +4 uranium ions. The data also indicates that there is an electronic difference between the bis(diamide)-THF uranium complexes as opposed to those that only contain one diamide and two cyclopentadienyl rings. Finally, magnetic measurements reveal that all complexes display temperature-dependent behavior consistent with uranium(IV) ions that do not include ligand radicals. Overall, this study determines that there is no significant bonding difference between the redox-innocent and redox-active ligand frameworks on uranium. Furthermore, there are no data to suggest covalent bonding character using the latter ligand framework on uranium, despite what is known for transition metals.

Interpretation of detailed aerial gamma-ray survey, Jabal Ashirah area, southeastern Arabian Shield, Kingdom of Saudi Arabia

USGS Publications Warehouse

Duval, J.S.

1987-01-01

A detailed aerial gamma-ray spectrometric survey of the Jabal Ashirah area in the southeastern Arabian Shield has been analyzed using computer-classification algorithms. The analysis resulted in maps that show radiometric map units and gamma-ray anomalies indicating the presence of possible concentrations of potassium and uranium. The radiometric-unit map was interpreted to 'produce a simplified radiolithic map that was correlated with the mapped geology. The gamma-ray data show uranium anomalies that coincide with a tin-bearing granite, but known gold and nickel mineralization do not have any associated gamma-ray signatures.

METAL EXTRACTION PROCESS

DOEpatents

Lewis, G.W. Jr.; Rhodes, D.E.

1957-11-01

An improved method for extracting uranium from aqueous solutions by solvent extraction is presented. A difficulty encountered in solvent extraction operations using an organic extractant (e.g., tributyl phosphate dissolved in kerosene or carbon tetrachloride) is that emulsions sometimes form, and phase separation is difficult or impossible. This difficulty is overcome by dissolving the organic extractant in a molten wax which is a solid at operating temperatures. After cooling, the wax which now contains the extractant, is broken into small particles (preferably flakes) and this wax complex'' is used to contact the uranium bearing solutions and extract the metal therefrom. Microcrystalline petroleum wax and certain ethylene polymers have been found suitable for this purpose.

Effects of hauling timber, lignite coal, and coke fuel on Louisiana highways and bridges.

DOT National Transportation Integrated Search

2005-03-01

This study included the development of a methodology to assess the economic impact of overweight permitted vehicles hauling timber, lignite coal, and coke fuel on Louisiana highways and bridges. Researchers identified the highway routes and bridges b...

Broiler Litter × Industrial By-Products Reduce Nutrients and Microbial Losses in Surface Runoff When Applied to Forages.

PubMed

Adeli, Ardeshir; Read, John J; Brooks, John P; Miles, Dana; Feng, Gary; Jenkins, Johnie N

2017-03-01

The inability to incorporate broiler litter (BL) into permanent hayfields and pastures leads to nutrient accumulation near the soil surface and increases the potential transport of nutrients in runoff. This study was conducted on Marietta silt loam soil to determine the effect of flue gas desulfurization (FGD) gypsum and lignite on P, N, C, and microbial concentrations in runoff. Treatments were (i) control (unfertilized) and (ii) BL at 13.4 Mg ha alone or (iii) treated with either FGD gypsum or lignite applied at 20% (w/w) (2.68 Mg ha). Rainfall simulators were used to produce a 5.6 cm h storm event sufficient in duration to cause 15 min of continuous runoff. Repeated rains were applied at 3-d intervals to determine how long FGD gypsum and lignite are effective in reducing loss of litter-derived N, P, and C from soil. Application of BL increased N, P, and C concentrations in runoff as compared to the control. Addition of FGD gypsum reduced ( < 0.05) water-soluble P and dissolved organic C concentrations in runoff by 39 and 16%, respectively, as compared to BL alone. Lignite reduced runoff total N and NH-N concentrations by 38 and 70%, respectively, as compared to BL alone. Addition of FGD gypsum or lignite failed to significantly reduce microbial loads in runoff, although both treatments reduced microbial concentration by >20%. Thus, BL treated with FGD and lignite can be considered as cost-effective management practices in the mitigation of P, N, and C and possibly microbial concentration in runoff. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

Uranium decay daughters from isolated mines: Accumulation and sources.

PubMed

Cuvier, A; Panza, F; Pourcelot, L; Foissard, B; Cagnat, X; Prunier, J; van Beek, P; Souhaut, M; Le Roux, G

2015-11-01

This study combines in situ gamma spectrometry performed at different scales, in order to accurately locate the contamination pools, to identify the concerned radionuclides and to determine the distribution of the contaminants from soil to bearing phase scale. The potential mobility of several radionuclides is also evaluated using sequential extraction. Using this procedure, an accumulation area located downstream of a former French uranium mine and concentrating a significant fraction of radioactivity is highlighted. We report disequilibria in the U-decay chains, which are likely related to the processes implemented on the mining area. Coupling of mineralogical analyzes with sequential extraction allow us to highlight the presence of barium sulfate, which may be the carrier of the Ra-226 activities found in the residual phase (Ba(Ra)SO4). In contrast, uranium is essentially in the reducible fraction and potentially trapped in clay-iron coatings located on the surface of minerals. Copyright © 2015 Elsevier Ltd. All rights reserved.

Physical exploration for uranium during 1951 in the Silver Reef district, Washington County, Utah

USGS Publications Warehouse

Stugard, Frederick

1953-01-01

During 1951 a joint exploration program of the most promising uraniferous areas in the Silver Reef district was made by the U.S. Geological Survey and the u.S. Atomic Energy Commission.  A U.S. Bureau of Mines drill crew, on contract to the Atomic Energy Commission, did 2,450 feet of diamond drilling under the geological supervision of the U.S. Geological Survey.  The purpose of the drilling was to delineate broadly the favorable ground for commercial development of the uranium depostis.  Ten drill holes were located around Pumpkin Point, which is the northeastern end of Buckeye Reef, to probe for extensions of small ore shootsmined on the Point in fine-grained sandstones of the Chinle formation.  Three additional holes were located around teh Tecumseh Hill to prbe for extensions of the small showings of uranium-bearing rocks of Buckeye Reef.

Lignite-to-methanol: an engineering evaluation of Winkler gasification and ICI methanol synthesis route. Final report

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

Goyen, S.; Baily, E.; Mawer, J.

1980-10-01

The objective of the work reported herein was to develop a preliminary conceptual design, capital requirements, and product cost for a lignite-to-methanol plant incorporating Winkler Gasification Technology and ICI Methanol synthesis. The lignite-to-methanol complex described herein is designed to produce 15,000 TPD of fuel grade methanol. The complex is designed to be self-sufficient with respect to all utility services, offsites, and other support facilities, including power generation. Following is a summary of the results of the study: (1) Tons per day (TPD) of Lignite Feedstock and Fuel (as received) was 47,770; (2) TPD of Fuel Grade Methanol Product was 15,000;more » (3) Thermal efficiency, % (HHV) was 47.4; (4) Plant investment expressed in terms of first quarter of 1980 was ($ Million) 1545; and (5) Applying the economic premises used by EPRI for fuel conversion plant utility type financing, the calculated levelized and first year product costs are included.« less

Combustion behavior of different kinds of torrefied biomass and their blends with lignite.

PubMed

Toptas, Asli; Yildirim, Yeliz; Duman, Gozde; Yanik, Jale

2015-02-01

In this study, the combustion behavior of different kinds of torrefied biomass (lignocellulosic and animal wastes) and their blends with lignite was investigated via non-isothermal thermogravimetric method under air atmosphere. For comparison, combustion characteristics of raw biomasses were also determined. Torrefaction process improved the reactivity of char combustion step of biomasses. Characteristic combustion parameters for blends showed non-additivity behavior. It was found that the mixture of torrefied biomasses and lignite at a ratio of 1:1 had a lower ignition and burnout temperature than the coal-only sample. Although no interactions were observed between the lignite and torrefied biomass at initial step of combustion, a certain degree of interaction between the components occurred at char combustion step. Kinetic parameters of combustion were calculated by using the Coats Redfern model. Overall, this study showed that poultry litters can be used as a substitute fuel in coal/biomass co-firing systems by blending with lignocellulosic biomass. Copyright © 2014 Elsevier Ltd. All rights reserved.

Thermogravimetric investigation of the co-combustion between the pyrolysis oil distillation residue and lignite.

PubMed

Li, Hao; Xia, Shuqian; Ma, Peisheng

2016-10-01

Co-combustion of lignite with distillation residue derived from rice straw pyrolysis oil was investigated by non-isothermal thermogravimetric analysis (TGA). The addition of distillation residue improved the reactivity and combustion efficiency of lignite, such as increasing the weight loss rate at peak temperature and decreasing the burnout temperature and the total burnout. With increasing distillation residue content in the blended fuels, the synergistic interactions between distillation residue and lignite firstly increased and then decreased during co-combustion stage. Results of XRF, FTIR, (13)C NMR and SEM analysis indicated that chemical structure, mineral components and morphology of samples have great influence on the synergistic interactions. The combustion mechanisms and kinetic parameters were calculated by the Coats Redfern model, suggesting that the lowest apparent activation energy (120.19kJ/mol) for the blended fuels was obtained by blending 60wt.% distillation residue during main co-combustion stage. Copyright © 2016 Elsevier Ltd. All rights reserved.

Petrographic Composition of Lignite from the Lake Somerville Spillway (East-central Texas)

NASA Astrophysics Data System (ADS)

Pawelec, Sandra; Bielowicz, Barbara

2017-12-01

In the presented paper, the macroscopic and microscopic composition of lignite from Lake Somerville Spillway has been examined. The study area is the upper part of the Manning Formation, located north-west of Somerville in the central-eastern part of Texas. There are three exposures: NE, SW and MC (Main Central) with visible parts of late-Eocene lignite seams belonging to the Jackson Group. The Manning section is divided into four marine dominated parasequences (P1 through P4). Lignite samples outlining the P1 parasequence from the MC and NE outcrops and the argillate sample from the lower part of the P2 parasequence, NE outcrop. Macroscopic characterization was carried out based on lithological classifications of humic coal. On this basis, it has been shown that the main lithotype occurring in the deposit is detritic (matrix) coal with a high share of mineral matter. The maceral composition of coal was determined according to the ICCP guidelines. The macerals from liptinite group were determined under fluorescent light. The maceral group content analysis was performed with use of 500-600 equally spaced points on the surface of the polished sections. It has been found that the examined coal is dominated by macerals from the huminite group, with a share ranging from 20.8 to 65.3% volume, including atrinite (9.8-22.8% volume, 17.5% volume on average). In the examined coal, macerals from the inertinite group (10.1 to 44.8%), especially semifusinite (max. 13.9%), fusinite (max. 9.3%) and funginite (max. 6.3 %) are of particularly large share. In the liptinite group, particular attention was paid to the content of alginite (max. 4.5%) and bituminite (max. 1.3 %), which indicate the paralic sedimentation environment of the examined coal. Additionally, the variability of macerals and maceral groups within the exposures and levels of the P1 parasequence was examined. The last step was to compare lignite from Lake Somerville Spillway with other lignites belonging to the Jackson Group, namely Gibbons Creek and San Miguel lignite mines.

The application of Airborne Laser Scaning for identifying old lignite workings - case study: the mine "Borussia" near Ośno Lubuskie (Western Poland)

NASA Astrophysics Data System (ADS)

Gontaszewska-Piekarz, Agnieszka; Mrówczyńska, Maria

2018-04-01

The paper presents the possibilities of using data obtained by airborne laser scanning for identifying areas where lignite used to be mined. The technology of airborne laser scanning presented in the paper as and its results have a vast potential in terms of identifying local terrain deformations. The paper also presents the history of lignite mining in the region of Ośno Lubuskie (the north-west of Ziemia Lubuska - western Poland). It describes underground mining in complicated geological conditions (glaciotectonic deformations). The paper is supplemented with historical maps showing the locations of the mines

Production of Polyhydroxyalkanoates Using Hydrolyzates of Spruce Sawdust: Comparison of Hydrolyzates Detoxification by Application of Overliming, Active Carbon, and Lignite

PubMed Central

Kucera, Dan; Benesova, Pavla; Ladicky, Peter; Pekar, Miloslav; Sedlacek, Petr; Obruca, Stanislav

2017-01-01

Polyhydroxyalkanoates (PHAs) are bacterial polyesters which are considered biodegradable alternatives to petrochemical plastics. PHAs have a wide range of potential applications, however, the production cost of this bioplastic is several times higher. A major percentage of the final cost is represented by the price of the carbon source used in the fermentation. Burkholderia cepacia and Burkholderia sacchari are generally considered promising candidates for PHA production from lignocellulosic hydrolyzates. The wood waste biomass has been subjected to hydrolysis. The resulting hydrolyzate contained a sufficient amount of fermentable sugars. Growth experiments indicated a strong inhibition by the wood hydrolyzate. Over-liming and activated carbon as an adsorbent of inhibitors were employed for detoxification. All methods of detoxification had a positive influence on the growth of biomass and PHB production. Furthermore, lignite was identified as a promising alternative sorbent which can be used for detoxification of lignocellulose hydrolyzates. Detoxification using lignite instead of activated carbon had lower inhibitor removal efficiency, but greater positive impact on growth of the bacterial culture and overall PHA productivity. Moreover, lignite is a significantly less expensive adsorbent in comparison with activated charcoal and; moreover, used lignite can be simply utilized as a fuel to, at least partially, cover heat and energetic demands of fermentation, which should improve the economic feasibility of the process. PMID:28952532

Germanium and uranium in coalified wood from Upper Devonian black shale

USGS Publications Warehouse

Breger, Irving A.; Schopf, James M.

1954-01-01

Microscopic study of black, vitreous, carbonaceous material occurring in the Chattanooga shale in Tennessee and in the Cleveland member of the Ohio shale in Ohio has revealed coalified woody plant tissue. Some samples have shown sufficient detail to be identified with the genus Callixylon. Similar material has been reported in the literature as "bituminous" or "asphaltic" stringers. Spectrographic analyses of the ash from the coalified wood have shown unusually high percentages of germanium, uranium, vanadium, and nickel. The inverse relationship between uranium and germanium in the ash and the ash content of various samples shows an association of these elements with the organic constituents of the coal. On the basis of geochemical considerations, it seems most probable that the wood or coalified wood was germanium-bearing at the time logs or woody fragments were floated into the basins of deposition of the Chattanooga shale and the Cleveland member of the Ohio shale. Once within the marine environment, the material probably absorbed uranium with the formation of organo-uranium compounds such as have been found to exist in coals. It is suggested that a more systematic search for germaniferous coals in the vicinity of the Chattanooga shale and the Cleveland member of the Ohio shale might be rewarding.

ALPHA SPECTROMETRIC EVALUATION OF SRM-995 AS A POTENTIAL URANIUM/THORIUM DOUBLE TRACER SYSTEM FOR AGE-DATING URANIUM MATERIALS

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

Beals, D.

2011-12-06

Uranium-233 (t{sub 1/2} {approx} 1.59E5 years) is an artificial, fissile isotope of uranium that has significant importance in nuclear forensics. The isotope provides a unique signature in determining the origin and provenance of uranium-bearing materials and is valuable as a mass spectrometric tracer. Alpha spectrometry was employed in the critical evaluation of a {sup 233}U standard reference material (SRM-995) as a dual tracer system based on the in-growth of {sup 229}Th (t{sub 1/2} {approx} 7.34E3 years) for {approx}35 years following radiochemical purification. Preliminary investigations focused on the isotopic analysis of standards and unmodified fractions of SRM-995; all samples were separatedmore » and purified using a multi-column anion-exchange scheme. The {sup 229}Th/{sup 233}U atom ratio for SRM-995 was found to be 1.598E-4 ({+-} 4.50%) using recovery-corrected radiochemical methods. Using the Bateman equations and relevant half-lives, this ratio reflects a material that was purified {approx} 36.8 years prior to this analysis. The calculated age is discussed in contrast with both the date of certification and the recorded date of last purification.« less

National Uranium Resource Evaluation: Marfa Quadrangle, Texas

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

Henry, C D; Duex, T W; Wilbert, W P

1982-09-01

The uranium favorability of the Marfa 1/sup 0/ by 2/sup 0/ Quadrangle, Texas, was evaluated in accordance with criteria established for the National Uranium Resource Evaluation. Surface and subsurface studies, to a 1500 m (5000 ft) depth, and chemical, petrologic, hydrogeochemical, and airborne radiometric data were employed. The entire quadrangle is in the Basin and Range Province and is characterized by Tertiary silicic volcanic rocks overlying mainly Cretaceous carbonate rocks and sandstones. Strand-plain sandstones of the Upper Cretaceous San Carlos Formation and El Picacho Formation possess many favorable characteristics and are tentatively judged as favorable for sandstone-type deposits. The Tertiarymore » Buckshot Ignimbrite contains uranium mineralization at the Mammoth Mine. This deposit may be an example of the hydroauthigenic class; alternatively, it may have formed by reduction of uranium-bearing ground water produced during diagenesis of tuffaceous sediments of the Vieja Group. Although the presence of the deposit indicates favorability, the uncertainty in the process that formed the mineralization makes delineation of a favorable environment or area difficult. The Allen intrusions are favorable for authigenic deposits. Basin fill in several bolsons possesses characteristics that suggest favorability but which are classified as unevaluated because of insufficient data. All Precambrian, Paleozoic, other Mesozoic, and other Cenozoic environments are unfavorable.« less

Radium and uranium concentrations and associated hydrogeochemistry in ground water in southwestern Pueblo County, Colorado

USGS Publications Warehouse

Felmlee, J. Karen; Cadigan, Robert Allen

1979-01-01

Radium and uranium concentrations in water from 37 wells tapping the aquifer system of the Dakota Sandstone and Purgatoire Formation in southwestern Pueblo County, Colorado, have a wide range of values and define several areas of high radioactivity in the ground water. Radium ranges from 0.3 to 420 picocuries per liter and has a median value of 8.8, and uranium ranges from 0.02 to 180 micrograms per liter and has a median value of 2.4. Radon concentrations, measured in 32 of the 37 wells, range from less than 100 picocuries per liter to as much as 27,000 and have a median value of 580. Relationships among the radioactive elements and 28 other geochemical parameters were studied by using correlation coefficients and R-mode factor analysis. Five factor groups were determined to represent major influences on water chemistry: (1) short-term solution reactions, (2) oxidation reactions, (3) hydrolysis reactions, (4) uranium distribution, and (5) long-term solution reactions. Uranium concentrations are most strongly influenced by oxidation reactions but also are affected by solution reactions and distribution of uranium in the rocks of the aquifer system. Radon and radium concentrations are mostly controlled by uranium distribution; radium also shows a moderate negative relationship with oxidation. To explain the statistical and spatial relationships among the parameters, a model was developed involving the selective leaching of uranium-bearing phases and metal sulfides which occur in discontinuous zones in sandstone and shale. When reducing conditions prevail, uranium is immobile, but radium can be taken into solution. When faults and associated fractured rocks allow oxidizing conditions to dominate, uranium can be taken into solution; radium can also be taken into solution, or it may become immobilized by coprecipitation with iron and manganese oxides or with barite. Several areas within the study area are discussed in terms of the model.

Uranium isotope separation from 1941 to the present

NASA Astrophysics Data System (ADS)

Maier-Komor, Peter

2010-02-01

Uranium isotope separation was the key development for the preparation of highly enriched isotopes in general and thus became the seed for target development and preparation for nuclear and applied physics. In 1941 (year of birth of the author) large-scale development for uranium isotope separation was started after the US authorities were warned that NAZI Germany had started its program for enrichment of uranium and might have confiscated all uranium and uranium mines in their sphere of influence. Within the framework of the Manhattan Projects the first electromagnetic mass separators (Calutrons) were installed and further developed for high throughput. The military aim of the Navy Department was to develop nuclear propulsion for submarines with practically unlimited range. Parallel to this the army worked on the development of the atomic bomb. Also in 1941 plutonium was discovered and the production of 239Pu was included into the atomic bomb program. 235U enrichment starting with natural uranium was performed in two steps with different techniques of mass separation in Oak Ridge. The first step was gas diffusion which was limited to low enrichment. The second step for high enrichment was performed with electromagnetic mass spectrometers (Calutrons). The theory for the much more effective enrichment with centrifugal separation was developed also during the Second World War, but technical problems e.g. development of high speed ball and needle bearings could not be solved before the end of the war. Spying accelerated the development of uranium separation in the Soviet Union, but also later in China, India, Pakistan, Iran and Iraq. In this paper, the physical and chemical procedures are outlined which lead to the success of the project. Some security aspects and Non-Proliferation measures are discussed.

Geophysical interpretation of U, Th, and rare earth element mineralization of the Bokan Mountain peralkaline granite complex, Prince of Wales Island, southeast Alaska

USGS Publications Warehouse

McCafferty, Anne E.; Stoeser, Douglas B.; Van Gosen, Bradley S.

2014-01-01

A prospectivity map for rare earth element (REE) mineralization at the Bokan Mountain peralkaline granite complex, Prince of Wales Island, southeastern Alaska, was calculated from high-resolution airborne gamma-ray data. The map displays areas with similar radioelement concentrations as those over the Dotson REE-vein-dike system, which is characterized by moderately high %K, eU, and eTh (%K, percent potassium; eU, equivalent parts per million uranium; and eTh, equivalent parts per million thorium). Gamma-ray concentrations of rocks that share a similar range as those over the Dotson zone are inferred to locate high concentrations of REE-bearing minerals. An approximately 1300-m-long prospective tract corresponds to shallowly exposed locations of the Dotson zone. Prospective areas of REE mineralization also occur in continuous swaths along the outer edge of the pluton, over known but undeveloped REE occurrences, and within discrete regions in the older Paleozoic country rocks. Detailed mineralogical examinations of samples from the Dotson zone provide a means to understand the possible causes of the airborne Th and U anomalies and their relation to REE minerals. Thorium is sited primarily in thorite. Uranium also occurs in thorite and in a complex suite of ±Ti±Nb±Y oxide minerals, which include fergusonite, polycrase, and aeschynite. These oxides, along with Y-silicates, are the chief heavy REE (HREE)-bearing minerals. Hence, the eU anomalies, in particular, may indicate other occurrences of similar HREE-enrichment. Uranium and Th chemistry along the Dotson zone showed elevated U and total REEs east of the Camp Creek fault, which suggested the potential for increased HREEs based on their association with U-oxide minerals. A uranium prospectivity map, based on signatures present over the Ross-Adams mine area, was characterized by extremely high radioelement values. Known uranium deposits were identified in the U-prospectivity map, but the largest tract occurs over a radioelement-rich granite phase within the pluton that is likely not related to mineralization. Neither mineralization type displays a well-defined airborne magnetic signature.

The Nopal 1 Uranium Deposit: an Overview

NASA Astrophysics Data System (ADS)

Calas, G.; Allard, T.; Galoisy, L.

2007-05-01

The Nopal 1 natural analogue is located in the Pena Blanca uranium district, about 50 kms north of Chihuahua City, Mexico. The deposit is hosted in tertiary ignimbritic ash-flow tuffs, dated at 44 Ma (Nopal and Colorados formations), and overlying the Pozos conglomerate formation and a sequence of Cretaceous carbonate rocks. The deposit is exposed at the ground surface and consists of a near vertical zone extending over about 100 m with a diameter of 40 m. An interesting characteristic is that the primary mineralization has been exposed above the water table, as a result of the uplift of the Sierra Pena Blanca, and subsequently oxidized with a remobilization of hexavalent uranium. The primary mineralization has been explained by various genetic models. It is associated to an extensive hydrothermal alteration of the volcanic tuffs, locally associated to pyrite and preserved by an intense silicification. Several kaolinite parageneses occur in fissure fillings and feldspar pseudomorphs, within the mineralized breccia pipe and the barren surrounding rhyolitic tuffs. Smectites are mainly developed in the underlying weakly welded tuffs. Several radiation-induced defect centers have been found in these kaolinites providing a unique picture of the dynamics of uranium mobilization (see Allard et al., this session). Another evidence of this mobilization is given by the spectroscopy of uranium-bearing opals, which show characteristic fluorescence spectra of uranyl groups sorbed at the surface of silica. By comparison with the other uranium deposits of the Sierra Pena Blanca and the nearby Sierra de Gomez, the Nopal 1 deposit is original, as it is one of the few deposits hving retained a reduced uranium mineralization.

Evolution of uranium distribution and speciation in mill tailings, COMINAK Mine, Niger.

PubMed

Déjeant, Adrien; Galoisy, Laurence; Roy, Régis; Calas, Georges; Boekhout, Flora; Phrommavanh, Vannapha; Descostes, Michael

2016-03-01

This study investigated the evolution of uranium distribution and speciation in mill tailings from the COMINAK mine (Niger), in production since 1978. A multi-scale approach was used, which combined high resolution remote sensing imagery, ICP-MS bulk rock analyses, powder X-ray diffraction, Scanning Electron Microscopy, Focused Ion Beam--Transmission Electron Microscopy and X-ray Absorption Near Edge Spectroscopy. Mineralogical analyses showed that some ore minerals, including residual uraninite and coffinite, undergo alteration and dissolution during tailings storage. The migration of uranium and other contaminants depends on (i) the chemical stability of secondary phases and sorbed species (dissolution and desorption processes), and (ii) the mechanical transport of fine particles bearing these elements. Uranium is stabilized after formation of secondary uranyl sulfates and phosphates, and adsorbed complexes on mineral surfaces (e.g. clay minerals). In particular, the stock of insoluble uranyl phosphates increases with time, thus contributing to the long-term stabilization of uranium. At the surface, a sulfate-cemented duricrust is formed after evaporation of pore water. This duricrust limits water infiltration and dust aerial dispersion, though it is enriched in uranium and many other elements, because of pore water rising from underlying levels by capillary action. Satellite images provided a detailed description of the tailings pile over time and allow monitoring of the chronology of successive tailings deposits. Satellite images suggest that uranium anomalies that occur at deep levels in the pile are most likely former surface duricrusts that have been buried under more recent tailings. Copyright © 2015 Elsevier B.V. All rights reserved.

Fabrication of thorium bearing carbide fuels

DOEpatents

Gutierrez, Rueben L.; Herbst, Richard J.; Johnson, Karl W. R.

1981-01-01

Thorium-uranium carbide and thorium-plutonium carbide fuel pellets have been fabricated by the carbothermic reduction process. Temperatures of 1750.degree. C. and 2000.degree. C. were used during the reduction cycle. Sintering temperatures of 1800.degree. C. and 2000.degree. C. were used to prepare fuel pellet densities of 87% and >94% of theoretical, respectively. The process allows the fabrication of kilogram quantities of fuel with good reproducibility of chemicals and phase composition. Methods employing liquid techniques that form carbide microspheres or alloying-techniques which form alloys of thorium-uranium or thorium-plutonium suffer from limitation on the quantities processed of because of criticality concerns and lack of precise control of process conditions, respectively.

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

Kin, B.; Dincer, S.; Kuyulu, A.

The authors report the reduction and removal of sulfur compounds from Can K{sub 4}, Keles and Agacli lignite samples, obtained from mines close to Istanbul, studied using chlorine gas. Water or mixtures of methyl chloroform-water and carbon tetrachloride-water were used as solvents. Chlorine gas was bubbled through a suspension of lignite sample in solvent for about 1 to 5 hrs. It was observed that removal of sulfur increased with increasing time. Chlorinolysis and the Meyers method were used separately to compare their effects on the reduction of sulfur from Agacli and Keles lignite samples. Chlorinolysis was found to be moremore » effective than the Meyers method in the removal of organic sulfur and thus the total sulfur.« less

Lignite Research Project.

ERIC Educational Resources Information Center

Robinson, Fred

Since it became known in l979 that the Arkansas Power and Light Company was going to build a large electricity generating plant near Hampton and that there would be a lignite mining operation established there to support the power plant, the Warren public schools have been preparing to meet the impact on the schools. Because it was assumed that…

Spectral Study of Modified Humic Acids from Lignite

NASA Astrophysics Data System (ADS)

Zherebtsov, Sergey; Malyshenko, Natalya; Bryukhovetskaya, Ludmila; Ismagilov, Zinfer

2017-11-01

The IR-Fourier, ESR and solid-state 13C NMR analysis are used for investigation of unmodified and modified humic acids obtained from Tisul lignite (the Kansko-Achinsk Basin). Treatment with Hydrogen peroxide used for modification of humic acids and it changes the functionalgroup composition of the humic acids and increases the sorptional capacity

Survival and growth of trees and shrubs on different lignite minesoils in Louisiana

Treesearch

James D. Haywood; Allan E. Tiarks; James P. Barnett

1993-01-01

In 1980, an experimental opencast lignite mine was developed to compare redistributed A horizon with three minesoil mixtures as growth media for woody plants. The three minesoil mixtures contained different amounts and types of overburden materials, and normal reclamation practices were followed. Loblolly pine (Pinus taeda, L.), sawtooth oak (

Limitations and plausibility of the Pliocene lignite hypothesis in explaining the etiology of Balkan endemic nephropathy.

PubMed

Maharaj, S V M

2014-01-01

Balkan endemic nephropathy (BEN) is a chronic, tubulointerstitial renal disease often accompanied by urothelial cancer that has a lethality of nearly 100%. One of the many factors that have been proposed to play an etiological role in BEN is exposure to organic compounds from Pliocene lignite coal deposits via the drinking water in endemic areas. The objective of this study was to systematically evaluate the role of the tenets of the Pliocene lignite hypothesis in the etiology of BEN in order to provide an improved understanding of the hypothesis for colleagues and patients alike. A comprehensive compilation of the possible limitations of the hypothesis, with each limitation addressed in turn is presented. The Pliocene lignite hypothesis can best account for, is consistent with, or has the potential to explain the evidence associated with the myriad of factors related to BEN. Residents of endemic areas are exposed to complex mixtures containing hundreds of organic compounds at varying doses and their potentially more toxic (including nephrotoxic) and/or carcinogenic metabolites; however, a multifactorial etiology of BEN appears most likely.

Hydrologic and geochemical data for the Big Brown lignite mine area, Freestone County, Texas

USGS Publications Warehouse

Dorsey, Michael E.

1985-01-01

Lignite mining in east and east-central Texas is increasing in response to increased energy needs throughout the State. Associated with the increase in mining activities is a greater need to know the effects of mining activities on the water quantity and quality of near-surface aquifers. The near-surface lignite beds mined at the Big Brown Lignite Mine are from the Calvert Bluff Formation of the Wilcox Group of Eocene age, which is a minor aquifer generally having water suitable for all uses, in eastern Freestone County, Texas. One of the potential hydro!ogic effects of surface-coal mining is a change in the quality of ground water associated with replacement of aquifer materials by mine spoils. The purpose of this report is to compile and categorize geologic, mineralogic, geochemical, and hydrologic data for the Big Brown Lignite Mine and surrounding area in east-central Texas. Included are results of pasteextract analyses, constituent concentrations in water from batch-mixing experiments, sulfur analyses, and minerals or mineral groups detected by X-ray diffraction in 12 spoil material samples collected from 3 locations at the mine site. Also, common-constituent and trace-constituent concentrations in water from eight selected wells, located updip and downdip from the mine, are presented. Dissolved-solids concentrations in water from batch-mixing experiments vary from 12 to 908 milligrams per liter. Water from selected wells contain dissolved-solids concentrations ranging from 75 to 510 milligrams per liter.

Reclamation of a lignite combustion waste disposal site with alders (Alnus sp.): assessment of tree growth and nutrient status within 10 years of the experiment.

PubMed

Pietrzykowski, Marcin; Woś, Bartłomiej; Pająk, Marek; Wanic, Tomasz; Krzaklewski, Wojciech; Chodak, Marcin

2018-06-01

Combustion wastes are characterised by extremely low N contents. Therefore, introduction of nitrogen-fixing species at the first stage of their biological reclamation is required. This paper presents an assessment of the growth parameters of alders (Alnus sp.) 10 years after their introduction to a disposal site of lignite combustion waste in Central Poland. Black (Alnus glutinosa) and grey alders (Alnus incana) were planted directly in the combustion waste. The soil amendment included three variants: control with pure combustion waste, admixture of lignite culm and addition of acid sand. Both alder species displayed good growth parameters comparable to those of alders in natural habitats. However, black alder had better growth parameters, such as stand density index (SDI), diameter at breast height (DBH) and height (H) than grey alder. The lignite amendment exerted a positive effect on tree growth, reflected in a higher SDI and H, whereas the acid sand amendment did not affect any of the growth parameters of the studied alder species. Despite the good growth parameters, the measured N:P and N:K ratios in the alder leaves largely differed from the optimal values indicating insufficient P and K supply at the combustion waste disposal site. This may pose a threat to further development of the introduced tree plantings. The introduction of alders along with the lignite addition into the planting holes seems to be a successful method of combustion waste revegetation.

Biochar and lignite affect H+-ATPase and H+-PPase activities in root tonoplast and nutrient contents of mung bean under salt stress.

PubMed

Torabian, Shahram; Farhangi-Abriz, Salar; Rathjen, Judith

2018-05-31

This research was conducted to evaluate effects of biochar (50 and 100 g kg -1 soil) and lignite (50 and 100 g kg -1 soil) treatments on H + -ATPase and H + -PPase activity of root tonoplast, nutrient content, and performance of mung bean under salt stress. High saline conditions increased H + -ATPase and H + -PPase activities in root tonoplast, sodium (Na) content, reactive oxygen species (H 2 O 2 and O 2 - ) generation, relative electrolyte leakage (REL) and 2,2-Diphenyl-1-picrylhydrazyl (DPPH) activity in root and leaf, but decreased relative water content (RWC), chlorophyll content index, leaf area, potassium (K), calcium (Ca), magnesium (Mg), zinc (Zn) and iron (Fe) content of plant tissues, root and shoot dry weight of mung bean. Lignite and biochar treatments decreased the H + -ATPase and H + -PPase activities of root tonoplast under salt stress. Moreover, these treatments increased the cation exchange capacity of soil and nutrient values in plant tissues. Biochar and lignite diminished the generation of reactive oxygen species and DPPH activity in root and leaf cells, and these superior effects improved chlorophyll content index, leaf area and growth of mung bean under both conditions. In general, the results of this study demonstrated that biochar and lignite decreased the entry of Na ion into the cells, enriched plant cells with nutrients, and consequently improved mung bean performance under salt toxicity. Copyright © 2018 Elsevier Masson SAS. All rights reserved.

Preparation and combustion of Yugoslavian lignite-water fuel, Task 7.35. Topical report, July 1991--December 1993

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

Anderson, C.M.; DeWall, R.A.; Ljubicic, B.R.

1994-03-01

Yugoslavia`s interest in lignite-water fuel (LWF) stems from its involvement in an unusual power project at Kovin in northern Serbia. In the early 1980s, Electric Power of Serbia (EPS) proposed constructing a 600-MW power plant that would be fueled by lignite found in deposits along and under the Danube River. Trial underwater mining at Kovin proved that the dredging operation is feasible. The dredging method produces a coal slurry containing 85% to 90% water. Plans included draining the water from the coal, drying it, and then burning it in the pulverized coal plant. In looking for alternative ways to utilizemore » the ``wet coal`` in a more efficient and economical way, a consortium of Yugoslavian companies agreed to assess the conversion of dredged lignite into a LWF using hot-water-drying (HWD) technology. HWD is a high-temperature, nonevaporative drying technique carried out under high pressure in water that permanently alters the structure of low-rank coals. Changes effected by the drying process include irreversible removal of moisture, micropore sealing by tar, and enhancement of heating value by removal of oxygen, thus, enhancement of the slurry ability of the coal with water. Physical cleaning results indicated a 51 wt % reduction in ash content with a 76 wt % yield for the lignite. In addition, physical cleaning produced a cleaned slurry that had a higher attainable solids loading than a raw uncleaned coal slurry. Combustion studies were then performed on the raw and physically cleaned samples with the resulting indicating that both samples were very reactive, making them excellent candidates for HWD. Bench-scale results showed that HWD increased energy densities of the two raw lignite samples by approximately 63% and 81%. An order-of-magnitude cost estimate was conducted to evaluate the HWD and pipeline transport of Kovin LWF to domestic and export European markets. Results are described.« less

Analysis of Suitability for Development of New Mining Field in Northern Part of Kosovo Lignite Basin - Sibovc / Analiza Możliwości Udostępnienia Nowego Obszaru Wybierania W Północnej Części Zagłębia Węgla Brunatnego Sibovc W Kosowie

NASA Astrophysics Data System (ADS)

Cehlár, Michal; Rybár, Radim; Pinka, Ján; Haxhiu, Lorik; Beer, Martin

2013-06-01

This review describes the possibility of development a new lignite deposit in northern Kosovo lignite basin - Sibovc. Analysis of the initial state briefly evaluates Kosovo energy sector, geomorphological conditions and quality of lignite from Sibovc deposit. With using Dataminesoft it was created geological model and approximate calculation of lignite reserves in the deposit. The data obtained from Dataminesoft were used as starting points of the financial analysis of project. The result of the analysis is exactly describe the qualitative and quantitative characteristics of deposit Sibovc compared to other deposits in the area and creating of geological model with productive horizons deposit of lignite. Based on these data lignite deposit Sibovc was classified, according to the classification of deposits the UN, as economical. W pracy tej omówiono możliwości udostępnienia nowego obszaru wybierania złoża węgla brunatnego (lignitu) w północnej części zagłębia węgla brunatnego Sibovc w Kosowie. W analizie stanu początkowego krótko scharakteryzowano sektor energetyczny Kosowa, warunki geo-morfologiczne oraz parametry jakościowe węgla brunatnego z zagłębia Sibovc. Przy pomocy pakietu Dataminesoft stworzono model geologiczny i przeprowadzono przybliżone obliczenia zasobów węgla brunatnego w złożu. Dane uzyskane przy zastosowaniu pakietu Dataminesoft zostały następnie wykorzystane jako dane wejściowe do analizy finansowej przedsięwzięcia. Na podstawie wyników analizy uzyskuje się jakościową i ilościową charakterystykę złoża w odniesieniu do pozostałych złóż w regionie. Opracowano model geologiczny ze szczegółowym wskazaniem poziomów wybierania lignitu. W oparciu o te dane dokonano klasyfikacji złoża węgla brunatnego (lignitu) w Sibovc zgodnie z międzynarodowymi zasadami klasyfikacji wykazując, że złoże będzie ekonomiczne.

Multivariate analysis of subsurface radiometric data in Rongsohkham area, East Khasi Hills district, Meghalaya (India): implication on uranium exploration.

PubMed

Kukreti, B M; Pandey, Pradeep; Singh, R V

2012-08-01

Non-coring based exploratory drilling was under taken in the sedimentary environment of Rangsohkham block, East Khasi Hills district to examine the eastern extension of existing uranium resources located at Domiasiat and Wakhyn in the Mahadek basin of Meghalaya (India). Although radiometric survey and radiometric analysis of surface grab/channel samples in the block indicate high uranium content but the gamma ray logging results of exploratory boreholes in the block, did not obtain the expected results. To understand this abrupt discontinuity between the two sets of data (surface and subsurface) multivariate statistical analysis of primordial radioactive elements (K(40), U(238) and Th(232)) was performed using the concept of representative subsurface samples, drawn from the randomly selected 11 boreholes of this block. The study was performed to a high confidence level (99%), and results are discussed for assessing the U and Th behavior in the block. Results not only confirm the continuation of three distinct geological formations in the area but also the uranium bearing potential in the Mahadek sandstone of the eastern part of Mahadek Basin. Copyright © 2012 Elsevier Ltd. All rights reserved.

Potential Treatment of Inflammatory and Proliferative Diseases by Ultra-Low Doses of Ionizing Radiations

PubMed Central

Sanders, Charles L.

2012-01-01

Ultra-low doses and dose- rates of ionizing radiation are effective in preventing disease which suggests that they also may be effective in treating disease. Limited experimental and anecdotal evidence indicates that low radiation doses from radon in mines and spas, thorium-bearing monazite sands and enhanced radioactive uranium ore obtained from a natural geological reactor may be useful in treating many inflammatory conditions and proliferative disorders, including cancer. Optimal therapeutic applications were identified via a literature survey as dose-rates ranging from 7 to 11μGy/hr or 28 to 44 times world average background rates. Rocks from an abandoned uranium mine in Utah were considered for therapeutic application and were examined by γ-ray and laser-induced breakdown fluorescence spectroscopy. The rocks showed the presence of transuranics and fission products with a γ-ray energy profile similar to aged spent uranium nuclear fuel (93% dose due to β particles and 7% due to γ rays). Mud packs of pulverized uranium ore rock dust in sealed plastic bags delivering bag surface β,γ dose-rates of 10–450 μGy/h were used with apparent success to treat several inflammatory and proliferative conditions in humans. PMID:23304108

Neutronics Studies of Uranium-bearing Fully Ceramic Micro-encapsulated Fuel for PWRs

DOE PAGES

George, Nathan M.; Maldonado, G. Ivan; Terrani, Kurt A.; ...

2014-12-01

Our study evaluated the neutronics and some of the fuel cycle characteristics of using uranium-based fully ceramic microencapsulated (FCM) fuel in a pressurized water reactor (PWR). Specific PWR lattice designs with FCM fuel have been developed that are expected to achieve higher specific burnup levels in the fuel while also increasing the tolerance to reactor accidents. The SCALE software system was the primary analysis tool used to model the lattice designs. A parametric study was performed by varying tristructural isotropic particle design features (e.g., kernel diameter, coating layer thicknesses, and packing fraction) to understand the impact on reactivity and resultingmore » operating cycle length. Moreover, to match the lifetime of an 18-month PWR cycle, the FCM particle fuel design required roughly 10% additional fissile material at beginning of life compared with that of a standard uranium dioxide (UO 2) rod. Uranium mononitride proved to be a favorable fuel for the fuel kernel due to its higher heavy metal loading density compared with UO 2. The FCM fuel designs evaluated maintain acceptable neutronics design features for fuel lifetime, lattice peaking factors, and nonproliferation figure of merit.« less

30 CFR 75.1319 - Weight of explosives permitted in boreholes in bituminous and lignite mines.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 30 Mineral Resources 1 2014-07-01 2014-07-01 false Weight of explosives permitted in boreholes in bituminous and lignite mines. 75.1319 Section 75.1319 Mineral Resources MINE SAFETY AND HEALTH ADMINISTRATION... 3 pounds except when blasting solid rock in its natural deposit. (b) The total weight of explosives...

30 CFR 75.1319 - Weight of explosives permitted in boreholes in bituminous and lignite mines.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 30 Mineral Resources 1 2011-07-01 2011-07-01 false Weight of explosives permitted in boreholes in bituminous and lignite mines. 75.1319 Section 75.1319 Mineral Resources MINE SAFETY AND HEALTH ADMINISTRATION... 3 pounds except when blasting solid rock in its natural deposit. (b) The total weight of explosives...

30 CFR 75.1319 - Weight of explosives permitted in boreholes in bituminous and lignite mines.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 30 Mineral Resources 1 2010-07-01 2010-07-01 false Weight of explosives permitted in boreholes in bituminous and lignite mines. 75.1319 Section 75.1319 Mineral Resources MINE SAFETY AND HEALTH ADMINISTRATION... 3 pounds except when blasting solid rock in its natural deposit. (b) The total weight of explosives...

30 CFR 75.1319 - Weight of explosives permitted in boreholes in bituminous and lignite mines.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 30 Mineral Resources 1 2012-07-01 2012-07-01 false Weight of explosives permitted in boreholes in bituminous and lignite mines. 75.1319 Section 75.1319 Mineral Resources MINE SAFETY AND HEALTH ADMINISTRATION... 3 pounds except when blasting solid rock in its natural deposit. (b) The total weight of explosives...

30 CFR 75.1319 - Weight of explosives permitted in boreholes in bituminous and lignite mines.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 30 Mineral Resources 1 2013-07-01 2013-07-01 false Weight of explosives permitted in boreholes in bituminous and lignite mines. 75.1319 Section 75.1319 Mineral Resources MINE SAFETY AND HEALTH ADMINISTRATION... 3 pounds except when blasting solid rock in its natural deposit. (b) The total weight of explosives...

Origin of the Mariano Lake uranium deposit, McKinley County, New Mexico

USGS Publications Warehouse

Fishman, Neil S.; Reynolds, Richard L.

1982-01-01

The Mariano Lake uranium deposit, hosted by the Brushy Basin Member of the Jurassic Morrison Formation, occurs in the trough of an east-west trending syncline at the western end of the Smith Lake-Mariano Lake group of uranium deposits near Crownpoint, New Mexico. The orebody, which contains abundant amorphous organic material, is situated on the reduced side of a regional reduction-oxidation (redox) interface. The presence of amorphous organic material suggests the orebody may represent a tabular (primary) deposit, whereas the close proximity of the orebody to the redox interface is suggestive that uranium was secondarily redistributed by oxidative processes from pre-existing tabular orebodies. Uranium contents correlate positively with both organic carbon and vanadium contents. Petrographic evidence and scanning electron microscope-energy dispersive analyses point to uranium residence in the epigentically introduced amorphous organic material, which coats detrital grains and fills voids. Uranium mineralization was preceded by the following diagenetic alterations: precipitation of pyrite (d34S values ranging from-11.0 to-38.2 per mil); precipitation of mixed-layer smectite-illite clays; partial dissolution of some of the detrital feldspar population; and precipitation of quartz and adularia overgrowths. Alterations associated with uranium mineralization include emplacement of amorphous organic material (possibly uranium bearing); destruction of detrital iron-titanium oxide grains; coprecipitation of chlorite and microcrystalline quartz, and precipitation of pyrite and marcasite (d34S values for these sulfides ranging from -29.4 to -41.6 per mil). After mineralization, calcite, dolomite, barite, and kaolinite precipitated, and authigenic iron disulfides were replaced by ferric oxides and hydroxides. Geochemical data (primarily the positive correlation of uranium content to both organic carbon and vanadium contents) and petrographic observations (epigentically introduced amorphous organic matter and uranium residence in this organic matter) indicate that the Mariano Lake orebody is a tabular-type uranium deposit. Oxidative processes have not noticeably redistributed and reconcentrated primary uranium in the immediate vicinity of the deposit nor have they greatly modified geochemical characteristics in the ore. Preservation of the Mariano Lake deposit may not only be related to its position along the synclinal trough, where oxidative destruction of the orebody has been inhibited by stagnation of oxidizing ground waters by the structure, but also due to the deflection of ground waters (resulting from low orebody porosity) around the orebody.

Correlation of Paleocene Harmon and Hansen lignite beds, Adams, Billings, Bowman, Golden Valley, Hettinger, and Slope Counties, Williston Basin, North Dakota

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

Keighin, C.W.; Flores, R.M.; Ochs, A.

In southwestern North Dakota, minable lignite beds in the Paleocene Fort Union Formation include the Harmon and Hansen beds in the Bowman-Gascoyne area. Data from more than 700 drill holes penetrating these beds was used to construct stratigraphic cross sections. The Harmon and Hansen beds are the thickest and most laterally persistent lignites found under < 150 ft of overburden. The Harmon coal bed is as much as 34 ft thick, and is often split by claystone interbeds of variable thickness. The Hansen coal bed typically occurs 10--100 ft below the Harmon coal bed; it rarely attains a thickness ofmore » 15 ft, and averages 4 ft in thickness.« less

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

Korkmaz, S.; Kara-Gulbay, R.; Turan, M.

Since Turkey is a developing country with tremendous economic growth, its energy demand is also getting increased. Of this energy, about 70% is supplied from fossil fuels and the remaining 30% is from renewable sources. Among the fossil fuels, 90% of oil, natural gas, and coal are imported, and only 10% is from domestic sources. All the lignite is supplied from domestic sources. The total share of renewable sources and lignite in the total energy production is 45%. In order for Turkey to have sufficient and reliable energy sources, first the renewable energy sources must be developed, and energy productionmore » from fossil fuels, except for lignite, must be minimized. Particularly, scarcity of fossil fuels and increasing oil prices have a strong effect on economic growth of the country.« less

A summary of niobium and rare earth localities from Ha'il and other areas in western Saudi Arabia: a preliminary study

USGS Publications Warehouse

Matzko, John J.; Naqvi, Mohammed Ibne

1978-01-01

Investigations in 1965 located veins containing radioactive material in the Halaban Group on the east side of a granite pluton at Jabal Aja near Ha'il. Later study extended the known area of radioactivity to a total length of about 30 km. Mineralogic studies indicated that the samples were low in uranium and that the radioactivity was due principally to thorium in niobium-bearing minerals. Two samples were reexamined to identify the sources of radioactivity, but X-ray and alpha plate studies did not reveal the radioactive minerals, even though uranium mineralization was indicated by the alpha plates. Further sampling is suggested to isolate the sources of radioactivity. This study indicates that niobium occurrences are related to alkaline intrusives in many areas of western Saudi Arabia. These areas should be investigated for their possible niobium and rare earth contents; their uranium content is apparently too low to be of economic interest.

Uranium-bearing breccia pipes of northwestern Arizona - an overview

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

Chenoweth, W.L.

During the 1950s and 1960s, the uranium deposits in breccia pipes of the Grand Canyon region were regarded as geologic curiosities. Today this area is the site of numerous exploration projects for ore-bearing pipes. The classic example of the older mines is the Orphan Lode, a patented claim within Grand Canyon National Park. Between 1956 and 1969, this deposit produced 4.26 million lb U/sub 3/O/sub 8/. Exploration since the mid-1970s has developed numerous new deposits in the Grand Canyon region. The Hack 1, 2, and 3, Pigeon, Kanab North, Canyon, and Pinenut deposits are, or will be, mined. The pipesmore » are circular and originated by dissolution of the Mississippian Redwall Limestone and collapse of the overlying strata. Uraninite ore occurs in both the pipe fill and in association with the peripheral shear zone. The principal host rocks are the Coconino Sandstone, Hermit Shale, and Esplanade Sandstone. Although small (3 to 5 million lb U/sub 3/O/sub 8/), the high grade (60 to 70% U/sub 3/O/sub 8/) of the deposits makes the pipes attractive exploration targets.« less

Uranium Isotope Ratios in Modern and Precambrian Soils

NASA Astrophysics Data System (ADS)

DeCorte, B.; Planavsky, N.; Wang, X.; Auerbach, D. J.; Knudsen, A. C.

2015-12-01

Uranium isotopes (δ238U values) are an emerging paleoredox proxy that can help to better understand the redox evolution of Earth's surface environment. Recently, uranium isotopes have been used to reconstruct ocean and atmospheric redox conditions (Montoya-Pino et al., 2010; Brennecka et al., 2011; Kendall et al., 2013; Dahl et al., 2014). However, to date, there have not been studies on paleosols, despite that paleosols are, arguably better suited to directly tracking the redox conditions of the atmosphere. Sedimentary δ238U variability requires the formation of the soluble, oxidized form of U, U(VI). The formation of U(VI) is generally thought to require oxygen levels orders of magnitude higher than prebiotic levels. Without significant U mobility, it would have been impossible to develop isotopically distinct pools of uranium in ancient Earth environments. Conversely, an active U redox cycle leads to significant variability in δ238U values. Here we present a temporally and geographically expansive uranium isotope record from paleosols and modern soils to better constrain atmospheric oxygen levels during the Precambrian. Preliminary U isotope measurements of paleosols are unfractionated (relative to igneous rocks), possibly because of limited fractionation during oxidation (e.g., {Wang, 2015 #478}) or insufficient atmospheric oxygen levels to oxidize U(IV)-bearing minerals in the bedrock. Further U isotope measurements of paleosols with comparison to modern soils will resolve this issue.

Geology and recognition criteria for uranium deposits of the quartz-pebble conglomerate type. Final report

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

Button, A.; Adams, S.S.

1981-03-01

This report is concerned with Precambrian uraniferous conglomerates. This class of deposit has been estimated to contain between approximately 16 and 35 percent of the global uranium reserve in two rather small areas, one in Canada, the other in South Africa. Similar conglomerates, which are often gold-bearing, are, however, rather widespread, being found in parts of most Precambrian shield areas. Data have been synthesized on the geologic habitat and character of this deposit type. The primary objective has been to provide the most relevant geologic observations in a structural fashion to allow resource studies and exploration to focus on themore » most prospective targets in the shortest possible time.« less

Uranium-series dating of the Mousterian occupation at Abric Romani, Spain

USGS Publications Warehouse

Bischoff, J.L.; Julia, R.; Mora, R.

1988-01-01

The precise evolutionary position of the Neanderthal people continues to be a major uncertainty in human evolution. Their origin and their relationship to anatomically modern people are unclear and are clouded by poor chronology. Lithic artefacts of' the Mousterian type, found throughout Europe and the Mediterranean Basin, are believed to be the tool kit of the Neanderthals, but dates within Mousterian-bearing deposits are extremely rare. We report here on 20 high-quality uranium-series dates from Mousterian beds at Abric Romani, a rock shelter near Barcelona, Spain. The dates range from 39 to 60 kyr before present (BP) in an orderly stratigraphic succession and provide precise chronological control on an important Mousterian archaeological site. ?? 1988 Nature Publishing Group.

Application of N-modified lignite and activated biochar to increase growth of summer wheat on nutrient-poor sandy soil

NASA Astrophysics Data System (ADS)

Schillem, Steffi; Schneider, Bernd-Uwe; Zeihser, Uwe; Hüttl, Reinhard F.

2017-04-01

Land degradation is recognized as the main environmental problem that adversely depletes soil organic carbon (SOC) and nitrogen (SON) stocks, which in turn directly affects the fertility and productivity of soils. Degraded soils and marginal lands are characterized by low fertility, poor physicochemical and biological properties and are almost free of soil organic matter (SOM), limiting their functional properties and, hence, their productivity. To enhance or restore the fertility of these soils, natural soil amendments such as biochar, lignite or humic acids can be added. A greenhouse experiment was carried out to investigate the effect of different application rates (5, 7.5, 11, 15, 28 t ha-1) of N-modified lignite (NL) incorporated in a nutrient-poor sandy soil from a recultivation site on plant growth, water use and nitrogen use efficiency of summer wheat. Additionally activated biochar (BC) was tested to see whether any differences exist between N-modified lignite and activated biochar at the same C-application rates. All variants with soil amendments displayed a much higher grain and straw yield and water use efficiency compared to the control sample. The differences were significant for the 28 t ha-1variant followed by the variant with 5 t ha-1 NL. With the 7.5 t ha-1 NL higher biomasses, water and nitrogen use efficiency could be achieved compared to the variant treated with BC at the same C-content. This study shows that even small amounts of N-modified lignite can increase growth, water and nitrogen use efficiency of summer wheat on marginal lands.

Comparison of metallurgical coke and lignite coke for power generation in Thailand

NASA Astrophysics Data System (ADS)

Ratanakuakangwan, Sudlop; Tangjitsitcharoen, Somkiat

2017-04-01

This paper presents and compares two alternatives of cokes in power generation which are the metallurgical coke with coke oven gas and the coke from lignite under the consideration of the energy and the environment. These alternatives not only consume less fuel due to their higher heat content than conventional coal but also has less SO2 emission. The metallurgical coke and its by-product which is coke oven gas can be obtained from the carbonization process of coking coal. According to high grade coking coal, the result in the energy attitude is not profitable but its sulfur content that directly affects the emission of SO2 is considered to be very low. On the other hand, the coke produced from lignite is known as it is the lowest grade from coal and it causes the high pollution. Regarding to energy profitability, the lignite coke is considered to be much more beneficial than the metallurgical coke in contrast to the environmental concerns. However, the metallurgical coke has the highest heating value. Therefore, a decision making between those choices must be referred to the surrounding circumstances based on energy and environment as well as economic consideration in the further research.

Limitations and plausibility of the Pliocene lignite hypothesis in explaining the etiology of Balkan endemic nephropathy

PubMed Central

Maharaj, S V M

2014-01-01

Background: Balkan endemic nephropathy (BEN) is a chronic, tubulointerstitial renal disease often accompanied by urothelial cancer that has a lethality of nearly 100%. Introduction: One of the many factors that have been proposed to play an etiological role in BEN is exposure to organic compounds from Pliocene lignite coal deposits via the drinking water in endemic areas. Objectives: The objective of this study was to systematically evaluate the role of the tenets of the Pliocene lignite hypothesis in the etiology of BEN in order to provide an improved understanding of the hypothesis for colleagues and patients alike. Methods: A comprehensive compilation of the possible limitations of the hypothesis, with each limitation addressed in turn is presented. Results: The Pliocene lignite hypothesis can best account for, is consistent with, or has the potential to explain the evidence associated with the myriad of factors related to BEN. Conclusions: Residents of endemic areas are exposed to complex mixtures containing hundreds of organic compounds at varying doses and their potentially more toxic (including nephrotoxic) and/or carcinogenic metabolites; however, a multifactorial etiology of BEN appears most likely. PMID:24075451

A geochemical study of macerals from a Miocene lignite and an Eocene bituminous coal, Indonesia

USGS Publications Warehouse

Stankiewicz, B.A.; Kruge, M.A.; Mastalerz, Maria

1996-01-01

Optical and chemical studies of maceral concentrates from a Miocene lignite and an Eocene high-volatile bituminous C coal from southeastern Kalimantan, Indonesia were undertaken using pyro-Lysis, optical, electron microprobe and FTIR techniques Pyrolysis products of vitrinite from bituminous coal were dominated by straight-chain aliphatics and phenols. The huminite of the Miocene lignite produced mostly phenolic compounds upon pyrolysis. Differences in the pyrolysis products between the huminite and vitrinite samples reflect both maturation related and paleobotanical differences. An undefined aliphatic source and/or bacterial biomass were the likely contributors of n-alkyl moieties to the vitrinite. The resinite fraction in the lignite yielded dammar-derived pyrolysis products, as well as aliphatics and phenols as the products of admixed huminite and other liptinites. The optically defined resinite-rich fraction of the bituminous coal from Kalimantan produced abundant n-aliphatic moieties upon pyrolysis, but only two major resin markers (cadalene and 1,6-dimethylnaphthalene). This phenomenon is likely due to the fact that Eocene resins were not dammar-related. Data from the electron microprobe and Fourier transform infrared spectrometry strongly support the results obtained by Py GC MS and microscopy.

Survey of synfuel technology for lignite

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

Sondreal, E.A.

1982-01-01

The most important market for lignite will continue to be the electric utility industry, where it is used to fuel large pc-fired boilers serving major regional power grids. However, the growth of this market and thechnology is being challenged by new and more stringent environmental control requirements, including the international concern over acid rain. Environmental and economic issues could either encourage or limit the development of a synfuels market for lignite depending on the cost effectiveness of the technological solutions that are developed. Clearly the United States needs to develop its coal resources to reduce dependence on imported oil. However,more » demand for coal derived substitute petroleum will be constrained by cost for the forseeable future. Government policy initiatives and new technology will be the keys to removing these constraints in the decades ahead. A crossover point with respect to petroleum and natural gas will be reached at some point in the future, which will allow synthetic fuels to penetrate the markets now served by oil and gas. Those of us who are today concerned with the development of lignite resources can look forward to participating in the major synfuels market that will emerge when those economic conditions are realized.« less

Uranium Bio-accumulation and Cycling as revealed by Uranium Isotopes in Naturally Reduced Sediments from the Upper Colorado River Basin

NASA Astrophysics Data System (ADS)

Lefebvre, Pierre; Noël, Vincent; Jemison, Noah; Weaver, Karrie; Bargar, John; Maher, Kate

2016-04-01

Uranium (U) groundwater contamination following oxidized U(VI) releases from weathering of mine tailings is a major concern at numerous sites across the Upper Colorado River Basin (CRB), USA. Uranium(IV)-bearing solids accumulated within naturally reduced zones (NRZs) characterized by elevated organic carbon and iron sulfide compounds. Subsequent re-oxidation of U(IV)solid to U(VI)aqueous then controls the release to groundwater and surface water, resulting in plume persistence and raising public health concerns. Thus, understanding the extent of uranium oxidation and reduction within NRZs is critical for assessing the persistence of the groundwater contamination. In this study, we measured solid-phase uranium isotope fractionation (δ238/235U) of sedimentary core samples from four study sites (Shiprock, NM, Grand Junction, Rifle and Naturita, CO) using a multi-collector inductively coupled plasma mass spectrometer (MC-ICP-MS). We observe a strong correlation between U accumulation and the extent of isotopic fractionation, with Δ238U up to +1.8 ‰ between uranium-enriched and low concentration zones. The enrichment in the heavy isotopes within the NRZs appears to be especially important in the vadose zone, which is subject to variations in water table depth. According to previous studies, this isotopic signature is consistent with biotic reduction processes associated with metal-reducing bacteria. Positive correlations between the amount of iron sulfides and the accumulation of reduced uranium underline the importance of sulfate-reducing conditions for U(IV) retention. Furthermore, the positive fractionation associated with U reduction observed across all sites despite some variations in magnitude due to site characteristics, shows a regional trend across the Colorado River Basin. The maximum extent of 238U enrichment observed in the NRZ proximal to the water table further suggests that the redox cycling of uranium, with net release of U(VI) to the groundwater by non-fractionating oxidation, is occurring within this zone. Thus, release of uranium from the NRZs may play a critical role in the persistence of groundwater contamination at these sites.

Beneficiation of Turkish lignites by thermal treatment and magnetic separation

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

Onal, G.; Renda, D.; Mustafaev, I.

1999-07-01

In this paper, the improvement of Turkish lignites by semi-coking and REMS magnetic separation, in two stages, is discussed. The oxidation and decomposition of pyrite through the thermal treatment result in the formation of iron oxide and pyrrhotite on the surface. In addition to pyrite, part of the organic sulfur is also removed. After thermal treatment of lignites at temperatures ranging from 370 to 650 C, the application of REMS magnetic separator produces a product higher in calorific value and lower in sulfur content. The product can be utilized after briquetting. The volatile gases can also be used after sulfurmore » removal. This process appears to be feasible as a clean coal manufacture from the point of energy efficiency. A short economic analysis is also presented.« less

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

Vorres, K S

The overall accomplishments of the HYGAS program to date are that it has demonstrated the key process concepts and integrated unit operations of coal gasification. It has also demonstrated several methods of hydrogen generation, including catalytic steam reforming of natural gas, electrothermal gasification, and also steam-oxygen gasification. A total of 37 tests with lignite, including a total of 5500 tons of lignite processed, demonstrated the technical feasibility of a gasification process using lignite. A total of 17 tests with bituminous coal involved a total of 3100 tons. Some specific objectives of the HYGAS program for fiscal 1977 include tests tomore » be conducted with subbituminous coal. Data will be collected for use in the design of an effluent treatment and water reuse cycles in a commercial plant. New methanation catalysts will be tested. Materials testing will continue.« less

Study on coal char ignition by radiant heat flux.

NASA Astrophysics Data System (ADS)

Korotkikh, A. G.; Slyusarskiy, K. V.

2017-11-01

The study on coal char ignition by CO2-continuous laser was carried out. The coal char samples of T-grade bituminous coal and 2B-grade lignite were studied via CO2-laser ignition setup. Ignition delay times were determined at ambient condition in heat flux density range 90-200 W/cm2. The average ignition delay time value for lignite samples were 2 times lower while this difference is larger in high heat flux region and lower in low heat flux region. The kinetic constants for overall oxidation reaction were determined using analytic solution of simplified one-dimensional heat transfer equation with radiant heat transfer boundary condition. The activation energy for lignite char was found to be less than it is for bituminous coal char by approximately 20 %.

RELATIONSHIP OF URANIUM ORE DEPOSITS TO PETROLEUM AND GAS-BEARING STRUCTURES

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

Russell, R.T.

eposits are located on producing or breached oil and gas structures, or in the immediate vicinity of such structures. Individual deposits associated with these structures contain ore reserves which may exceed one million tons. Data derived from a study of the known deposits should be useful in evaluating the potentiality of other areas where similar structural relations and abnormal radioactivity are known to exist. Uranium deposits located in producing oil or gas fields include a deposit of more than one million tons of uranium ore on a single salt dome in Texas, and uranium deposits in the Poison Basin, Wyoming,more » which are situated over a producing naturalgas structure, having a potential of 100,000 to 200,000 tons. Important uranium mining districts are also located near producing oil fields or near structures which may have contained oil at some time in the past. The Gas Hills district to Wyoming is on the flanks of a breached anticline and within one mile of natural-gas seeps. Deposits in the Brown's Park formation near Maybell, Colorado, are witin 10 miles of producing oil wells and natural-gas seeps are known within one mile of some of the uranium mines; and at Morrison, Colorado, uranium ore is associated with tar seeps. On th Colorado Plateau, large ore bodies with total reserves of at least 30 million tons of 0.3% U/sub 3/O/sub 8/ ore in the Ambrosia Lake district near Grants, New Mexico, and produce ore associated with asphaltite.'' The uraniferous asphaltite'' ore at Temple Mountain, Utah has been known for nearly 50 years. At both Circle Cliffs and the Inter- River area in Utah, uranium ore is associated with asphaltic material on anticlinal structures. Many other deposits are on breached strucIn Wyoming, uranium deposits in Tertiary sandstone and arkose generally lack carbon trash, but are located near oil or gas structures that contain hydrocarbons and natural gases capable of precititating uranium. Also, many uranium deposits on the Colorado Plateau have insufficient plant remains present to be the fixing agent for uranium, but petroleum and/or natural gas are proposed as possible extractants. The hydrogen sulfide contaned in natural gas or dissolved in oil-field water has been a factor in the formation of some uranium deposits. Oil-type structural traps must have been effective in localizing both petroleum and uranium ore in some districts. Although petroleum may contain small amounts of uranium, it is doubtful if either oil or natural gas are important transporting agents for uranium. Careful consideration of these various factors will provide a basis upon which to evaluate more effectively many ore producing areas. (auth)« less

Processes for liquefying carbonaceous feedstocks and related compositions

DOEpatents

MacDonnell, Frederick M.; Dennis, Brian H.; Billo, Richard E.; Priest, John W.

2017-02-28

Methods for the conversion of lignites, subbituminous coals and other carbonaceous feedstocks into synthetic oils, including oils with properties similar to light weight sweet crude oil using a solvent derived from hydrogenating oil produced by pyrolyzing lignite are set forth herein. Such methods may be conducted, for example, under mild operating conditions with a low cost stoichiometric co-reagent and/or a disposable conversion agent.

Enhancing Carbon Reactivity in Mercury Control in Lignite-Fired Systems

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

Chad Wocken; Michael Holmes; John Pavlish

2008-06-30

This project was awarded through the U.S. Department of Energy (DOE) National Energy Technology Laboratory Program Solicitation DE-PS26-03NT41718-01. The Energy & Environmental Research Center (EERC) led a consortium-based effort to resolve mercury (Hg) control issues facing the lignite industry. The EERC team-the Electric Power Research Institute (EPRI); the URS Corporation; the Babcock & Wilcox Company; ADA-ES; Apogee; Basin Electric Power Cooperative; Otter Tail Power Company; Great River Energy; Texas Utilities; Montana-Dakota Utilities Co.; Minnkota Power Cooperative, Inc.; BNI Coal Ltd.; Dakota Westmoreland Corporation; the North American Coal Corporation; SaskPower; and the North Dakota Industrial Commission-demonstrated technologies that substantially enhanced themore » effectiveness of carbon sorbents to remove Hg from western fuel combustion gases and achieve a high level ({ge} 55% Hg removal) of cost-effective control. The results of this effort are applicable to virtually all utilities burning lignite and subbituminous coals in the United States and Canada. The enhancement processes were previously proven in pilot-scale and limited full-scale tests. Additional optimization testing continues on these enhancements. These four units included three lignite-fired units: Leland Olds Station Unit 1 (LOS1) and Stanton Station Unit 10 (SS10) near Stanton and Antelope Valley Station Unit 1 (AVS1) near Beulah and a subbituminous Powder River Basin (PRB)-fired unit: Stanton Station Unit 1 (SS1). This project was one of three conducted by the consortium under the DOE mercury program to systematically test Hg control technologies available for utilities burning lignite. The overall objective of the three projects was to field-test and verify options that may be applied cost-effectively by the lignite industry to reduce Hg emissions. The EERC, URS, and other team members tested sorbent injection technologies for plants equipped with electrostatic precipitators (ESPs) and spray dryer absorbers combined with fabric filters (SDAs-FFs). The work focused on technology commercialization by involving industry and emphasizing the communication of results to vendors and utilities throughout the project.« less

Characteristics of Pyrolytic Topping in Fluidized Bed for Different Volatile Coals

NASA Astrophysics Data System (ADS)

Xiong, R.; Dong, L.; Xu, G. W.

Coal is generally combusted or gasified directly to destroy completely the chemical structures, such as aromatic rings containing in volatile coals including bituminite and lignite. Coal topping refers to a process that extracts chemicals with aromatic rings from such volatile coals in advance of combustion or gasification and thereby takes advantage of the value of coal as a kind of chemical structure resource. CFB boiler is the coal utilization facility that can be easily retrofitted to implement coal topping. A critical issue for performing coal topping is the choice of the pyrolytic reactor that can be different types. The present study concerns fluidized bed reactor that has rarely been tested for use in coal topping. Two different types of coals, one being Xiaolongtan (XLT) lignite and the other Shanxi (SX) bituminous, were tested to clarify the yield and composition of pyrolysis liquid and gas under conditions simulating actual operations. The results showed that XLT lignite coals had the maximum tar yield in 823-873K and SX bituminite realized its highest tar yield in 873-923K. Overall, lignite produced lower tar yield than bituminous coal. The pyrolysis gas from lignite coals contained more CO and CO2 and less CH4, H2 and C2+C3 (C2H4, C2H6, C3H6, C3H8) components comparing to that from bituminous coal. TG-FTIR analysis of tars demonstrated that for different coals there are different amounts of typical chemical species. Using coal ash of CFB boiler, instead of quartz sand, as the fluidized particles decreased the yields of both tar and gas for all the tested coals. Besides, pyrolysis in a reaction atmosphere simulating the pyrolysis gas (instead of N2) resulted also in higher production of pyrolysis liquid.

Catalysts and process developments for two-stage liquefaction. Fourth quarterly technical progress report, July 1, 1991--September 30, 1991

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

Cronauer, D.C.; Swanson, A.J.; Sajkowski, D.J.

Research under way in this project centers upon developing and evaluating catalysts and process improvements for coal liquefaction in the two-stage close-coupled catalytic process. As documented in the previous quarterly report there was little advantage for presoaking Black Thunder coal or Martin Lake lignite in a hydrogen-donor solvent, such as tetralin, at temperatures up to 600{degrees}F prior to liquefaction at higher temperatures. The amount of decarboxylation that occurred during the presoaking of Black Thunder coal or Martin Lake lignite in tetralin in the temperature range of 400 to 600{degrees}F was also relatively small. As indicated by both CO{sub 2} releasemore » and the change in oxygen-containing coal functionality, the level of decarboxylation in coal-derived solvent seems to correlate with the depth of coal dissolution. The feedstock liquefaction studies for the three feedstocks (Black Thunder subbituminous coal, Martin Lake lignite, and Illinois No. 6 coal) have been completed, and their results were compared in this report. Both Black Thunder coal and Martin Lake lignite gave lighter products than Illinois No. 6 coal at similar process conditions. Severe catalyst deactivation in the first stage was also observed with the Martin Lake lignite run. The first stage catalyst testing program was started. After a successful reference run with Illinois No. 6 coal, a high temperature run with AMOCAT{trademark} 1C was completed. In addition, a run was made with Illinois No. 6 coal using an oil-soluble catalyst, Molyvan L, in the first stage and AMOCAT{trademark} 1C in the second stage, where preliminary run results look promising.« less

Impact of RCRA (PL 94-580) on the use or disposal of solid wastes from Texas lignite-fired utility boilers: a literature survey. Final report. [Flue gas desulfurization sludges

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

Smith, R.L.

A literature survey was conducted in order to determine the amount of information available to the public concerning the impact of the Resource Conservation and Recovery Act of 1976 (RCRA) on the use or disposal of solid wastes from Texas lignite-fired utility boilers. The utility power plants of ALCOA, Big Brown, Martin Lake, Monticello and San Miguel are the only facilities currently using Texas lignite as fuel. RCRA is a comprehensive federal law which provides for the management of hazardous waste from generation to ultimate disposal. Utility solid wastes such as fly ash and flue gas desulfurization (FGD) sludge aremore » currently classified as excluded wastes (wastes exempt from hazardous classification) pending further information regarding these high-volume, low risk wastes. RCRA also provides for the increased need of recovered materials in Subtitle F - Federal Procurement. The lignite deposits of Texas occur in belts that stretch diagonally across the state from Laredo to Texarkana. The sulfur content and Btu value of Texas lignite combined requires that sulfur scrubbers be installed on new power plant units. The utility solid wastes occur in large quantities and leachate from some of these wastes contained detectable amounts of chromium and selenium. However, the concentration of these elements in the leachate was not sufficient to classify any of the utility wastes in this study as hazardous per current RCRA guidelines. In general, fly ash and FGD sludge are classified as Class II wastes and disposed of in an environmentally acceptable manner. Considerable amounts of bottom ash and fly ash are utilized but, thus far, FGD sludge has been landfilled, usually in combination with fly ash.« less

Characterizations of Deposited Ash During Co-Firing of White Pine and Lignite in Fluidized Bed Combustor

NASA Astrophysics Data System (ADS)

Shao, Yuanyuan; Zhu, Jesse; Preto, Fernando; Tourigny, Guy; Wang, Jinsheng; Badour, Chadi; Li, Hanning; Xu, Chunbao Charles

Characterizations of ash deposits from co-firing/co-combusting of a woody biomass (i.e., white pine) and lignite coal were investigated in a fluidized-bed combustor using a custom designed air-cooled probe installed in the freeboard region of the reactor. Ash deposition behaviors on a heat transfer surface were comprehensively investigated and discussed under different conditions including fuel type, fuel blending ratios (20-80% biomass on a thermal basis), and moisture contents. For the combustion of 100% lignite, the compositions of the deposited ash were very similar to those of the fuel ash, while in the combustion of 100% white pine pellets or sawdust the deposited ash contained a much lower contents of CaO, SO3, K2O and P2O5 compared with the fuel ash, but the deposited ash was enriched with SiO2, Al2O3 and MgO. A small addition of white pine (20% on a heat input basis) to the coal led to the highest ash deposition rates likely due to the strong interaction of the CaO and MgO (from the biomass ash) with the alumina and silica (from the lignite ash) during the co-combustion process, evidenced by the detection of high concentrations of calcium/magnesium sulfates, aluminates and silicates in the ash deposits. Interestingly, co-firing of white pine pellets and lignite at a 50% blending ratio led to the lowest ash deposition rates. Ash deposition rates in combustion of fuels as received with a higher moisture content was found to be much lower than those of oven-dried fuels.

Development of Kinetics and Mathematical Models for High-Pressure Gasification of Lignite-Switchgrass Blends: Cooperative Research and Development Final Report, CRADA Number CRD-11-447

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

Iisa, Kristiina

2016-04-06

NREL will work with Participant as a subtier partner under DE-FOA-0000240 titled "Co-Production of Power, Fuels, and Chemicals via Coal/Biomass Mixtures." The goal of the project is to determine the gasification characteristics of switchgrass and lignite mixtures and develop kinetic models. NREL will utilize a pressurized thermogravimetric analyzer to measure the reactivity of chars generated in a pressurized entrained-flow reactor at Participant's facilities and to determine the evolution of gaseous species during pyrolysis of switchgrass-lignite mixtures. Mass spectrometry and Fourier-transform infrared analysis will be used to identify and quantify the gaseous species. The results of the project will aid inmore » defining key reactive properties of mixed coal biomass fuels.« less

Impact of uranyl-calcium-carbonato complexes on uranium(VI) adsorption to synthetic and natural sediments.

PubMed

Stewart, Brandy D; Mayes, Melanie A; Fendorf, Scott

2010-02-01

Adsorption on soil and sediment solids may decrease aqueous uranium concentrations and limit its propensity for migration in natural and contaminated settings. Uranium adsorption will be controlled in large part by its aqueous speciation, with a particular dependence on the presence of dissolved calcium and carbonate. Here we quantify the impact of uranyl speciation on adsorption to both goethite and sediments from the Hanford Clastic Dike and Oak Ridge Melton Branch Ridgetop formations. Hanford sediments were preconditioned with sodium acetate and acetic acid to remove carbonate grains, and Ca and carbonate were reintroduced at defined levels to provide a range of aqueous uranyl species. U(VI) adsorption is directly linked to UO(2)(2+) speciation, with the extent of retention decreasing with formation of ternary uranyl-calcium-carbonato species. Adsorption isotherms under the conditions studied are linear, and K(d) values decrease from 48 to 17 L kg(-1) for goethite, from 64 to 29 L kg (-1) for Hanford sediments, and from 95 to 51 L kg(-1) for Melton Branch sediments as the Ca concentration increases from 0 to 1 mM at pH 7. Our observations reveal that, in carbonate-bearing waters, neutral to slightly acidic pH values ( approximately 5) and limited dissolved calcium are optimal for uranium adsorption.

PRIMARY MINERALIZATION OF URANIUM-BEARING "SILICEOUS REEF" VEINS IN THE BOULDER BATHOLITH, MONTANA. PART I. THE HOST ROCKS

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

Wright, H.D.; Bieler, B.H.

1960-01-01

Between 1952 and 1956 a study was made of some of the uranium-bearing hydrothermal veins in the northern part of the Boulder batholith, Montana. Three mines, the W. Wilson, G. Washington, and Free Enterprise, were investigated in detail. The veins are characterized by a microcrystalline quartz gangue containing sparsely scattered, very fine-grained sulfide minerals and uraninite. Above the present water table, secondary uranium minerals are abundant locally. Throughout the area the veins --called "siliceous reefs"--strike east to northeast, are of steep dip, and vary in thickness from a fraction of an inch to several feet. The country rock is granodioritemore » containing, in order of abundance, plagioclase (An/sub 30/ to An/sub 36/), quartz, orthoclase, biotite, and hornblende, with apatite, zircon, and sphene. Small bodies of aplite, pegmatite, and alaskite occur along some veins. The granodiorite adjacent to the veins is rather strongly altered. The alteration is similar throughout all of the deposits studied, in barren and orebearing portions alike. The essential minerals show a characteristic sequence of alteration, in the order hornblende, andesine, biotite, orthoclase, and quartz. Successive zones of alteration are characterized, from the vein outward, by maximum development of sericite (muscovite polytype 1M, in part), kaolinite, and montmorillonite. Other alteration products are quartz, pyrite, calcite, leucoxene, and chlorite. The alteration resulted in an increase in silica and ferric iron, a decrease in alumina, total iron, ferrous iron, lime, soda, and magnesia, and little change in potash, titania, phosphorus, carbon dioxide, and sulfur. Consideration of the stability fields of the sheet structure silicate minerals indicates little basis for interpretation of the temperatures prevailing during mineralization. (auth)« less

The Schlema-Alberoda five-element uranium deposit, Germany: An example of self-organizing hydrothermal system

NASA Astrophysics Data System (ADS)

Naumov, G. B.; Vlasov, B. P.; Golubev, V. N.; Mironova, O. F.

2017-01-01

As a result of integrating geological, mineralogical, and geochemical data on the unique Schlema-Alberoda five-element uranium deposit situated in Federal Republic of Germany and explored in detail down to a depth of 2 km, it has been shown that its formation for more than 100 Ma has been caused by combination of internal and external factors. The latter comprise favorable metallogenic specialization of the region, injection of intrusive bodies bearing the necessary stock of energy, and periodic pulses of tectonic reactivation. The internal factors of self-development involve evolutionary processes, which occur in host rocks at the consecutive stages of prograde and retrograde metamorphism giving rise to alteration of rocks in consistence with physical and chemical laws at variable temperature and degree of system opening.

Far Field Modeling Methods For Characterizing Surface Detonations

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

Garrett, A.

2015-10-08

Savannah River National Laboratory (SRNL) analyzed particle samples collected during experiments that were designed to replicate tests of nuclear weapons components that involve detonation of high explosives (HE). SRNL collected the particle samples in the HE debris cloud using innovative rocket propelled samplers. SRNL used scanning electronic microscopy to determine the elemental constituents of the particles and their size distributions. Depleted uranium composed about 7% of the particle contents. SRNL used the particle size distributions and elemental composition to perform transport calculations that indicate in many terrains and atmospheric conditions the uranium bearing particles will be transported long distances downwind.more » This research established that HE tests specific to nuclear proliferation should be detectable at long downwind distances by sampling airborne particles created by the test detonations.« less

The effects of pore structure on the behavior of water in lignite coal and activated carbon.

PubMed

Nwaka, Daniel; Tahmasebi, Arash; Tian, Lu; Yu, Jianglong

2016-09-01

The effects of physical structure (pore structure) on behavior of water in lignite coal and activated carbon (AC) samples were investigated by using Differential Scanning Calorimetry (DSC) and low-temperature X-ray diffraction (XRD) techniques. AC samples with different pore structures were prepared at 800°C in steam and the results were compared with that of parent lignite coal. The DSC results confirmed the presence of two types of freezable water that freeze at -8°C (free water) and -42°C (freezable bound water). A shift in peak position of free water (FW) towards lower temperature was observed in AC samples compared to the lignite coal with decreasing water loading. The amount of free water (FW) increased with increasing gasification conversion. The amounts of free and freezable bound water (FBW) in AC samples were calculated and correlated to pore volume and average pore size. The amount of FW in AC samples is well correlated to the pore volume and average pore size of the samples, while an opposite trend was observed for FBW. The low-temperature XRD analysis confirmed the existence of non-freezable water (NFW) in coal and AC with the boundary between the freezable and non-freezable water (NFW) determined. Copyright © 2016 Elsevier Inc. All rights reserved.

A field study of lignite as a drying aid in the superheated steam drying of anaerobically digested sludge.

PubMed

Hoadley, A F A; Qi, Y; Nguyen, T; Hapgood, K; Desai, D; Pinches, D

2015-10-01

Dried sludge is preferred when the sludge is either to be incinerated or used as a soil amendment. This paper focuses on superheated steam drying which has many benefits, because the system is totally enclosed, thereby minimising odours and particulate emissions. This work reports on field trials at a wastewater treatment plant where anaerobically digested sludge is dried immediately after being dewatered by belt press. The trials showed that unlike previous off-site tests, the sludge could be dried without the addition of a filter aid at a low production rate. However, the trials also confirmed that the addition of the lignite (brown coal) into the anaerobically digested sludge led to a more productive drying process, improved product quality and a greater fraction of the product being in the desired product size range. It is concluded that these results were achieved because the lignite helped to control the granule size in the dryer. Furthermore neither Salmonella spp or E coli were detected in the dried samples. Tests on spontaneous combustion show that this risk is increased in proportion to the amount of lignite used as a drying aid. Crown Copyright © 2015. Published by Elsevier Ltd. All rights reserved.

Ecohydrological perspective of phytogenic organic and inorganic components in Greek lignites: a quantitative reinterpretation

NASA Astrophysics Data System (ADS)

Mulder, Christian; Sakorafa, Vasiliki; Burragato, Francesco; Visscher, Henk

2000-06-01

A consensus about the development of freshwater wetlands in relation to time and space is urgently required. Our study aims to address this issue by providing additional data for a fine-scaled comparison of local depositional settings of Greek mires during the Pliocene and Pleistocene. Lignite profiles exhibit phytogenic organic components (macerals) that have been used to investigate the past peat-forming vegetation structure and their succession series. The organic petrology of lignite samples from the opencast mines of Komanos (Ptolemais) and Choremi (Megalopolis) was achieved to assess the water supply, wetland type, nutrient status and vegetation physiognomy. A holistic approach (a study of ecosystems as complete entities) was carried out for a paleoecological reconstruction of the mires. Huminite, liptinite and inertinite were traced by means of their chemical and morphological differences together with the morphogenic and taphonomic affinities. The problem of combining independent information from different approaches in a multivariate calibration setup has been considered. Linear regression, non-metric multidimensional scaling and one-way analysis of variance tested the occurrence of palynological and petrological proxies. Although the lignite formation and deposition are less related to humid periods than expected, the resulting differences occurring in the reconstructed development stages appear to be related to astronomically forced climate fluctuations.

Trace elements in the Fontinalis antipyretica from rivers receiving sewage of lignite and glass sand mining industry.

PubMed

Kosior, Grzegorz; Samecka-Cymerman, Aleksandra; Kolon, Krzysztof; Brudzińska-Kosior, Anna; Bena, Waldemar; Kempers, Alexander J

2015-07-01

Intensive lignite and glass sand mining and industrial processing release waste which may contain elements hazardous to the aquatic ecosystem and constitute a potential risk to human health. Therefore, their levels must be carefully controlled. As a result, we examined the effects of sewage on the aquatic Fontinalis antipyretica moss in the Nysa Łużycka (lignite industry) and the Kwisa Rivers (glass sand industry). The Nysa Łużycka and the Kwisa Rivers appeared to be heavily polluted with As, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, V and Zn, which were reflected in the extremely high concentration of these elements in F. antipyretica along the studied watercourses. In the Nysa Łużycka, trace element composition in the moss species is affected by lignite industry with accumulation in its tissues of the highest concentrations of Cd, Co, Cr, Cu, Mn, Ni, Pb and Zn, while samples from the Kwisa sites influenced by glass sand industry revealed the highest concentrations of As, V and Fe. The principal component and classification analysis classifies the concentration of elements in the aquatic F. antipyretica moss, thus enabling the differentiation of sources of water pollution in areas affected by mining industry.

Effect of co-combustion on the burnout of lignite/biomass blends: a Turkish case study.

PubMed

Haykiri-Acma, H; Yaman, S

2008-11-01

Co-combustion of Turkish Elbistan lignite and woody shells of hazelnut was performed in a TGA up to 1173 K with a heating rate of 20 K/min. SEM images of each fuel revealed the differences in their physical appearances. Hazelnut shell was blended with lignite in the range of 2-20 wt% to observe the co-combustion properties. Maximum burning rates (Rmax), temperatures of the maximum burning rates (T(R-max)), and the final burnout values of the parent samples and the blends were compared. The results were interpreted considering lignite properties and the major biomass ingredients such as cellulosics, hemicellulosics, and lignin. Deviations between the theoretical and experimental burnout values were evaluated at various temperatures. Burnout characteristics of the blends up to 10 wt% were concluded to have a synergistic effect so the addition of hazelnut shell up to 8 wt% provided higher burnouts than the expected theoretical ones, whereas addition of as much as 10 wt% led to a decrease in the burnout. However, the additive effects were more favorable for the blend having a biomass content of 20 wt%. Apparent activation energy, Rmax, and T(R-max), were found to follow the additive behavior for the blend samples.

Thermal exploitation of wastes with lignite for energy production.

PubMed

Grammelis, Panagiotis; Kakaras, Emmanuel; Skodras, George

2003-11-01

The thermal exploitation of wastewood with Greek lignite was investigated by performing tests in a laboratory-scale fluidized bed reactor, a 1-MW(th) semi-industrial circulating fluidized bed combustor, and an industrial boiler. Blends of natural wood, demolition wood, railroad sleepers, medium-density fiberboard residues, and power poles with lignite were used, and the co-combustion efficiency and the effect of wastewood addition on the emitted pollutants were investigated. Carbon monoxide, sulfur dioxide, and oxides of nitrogen emissions were continuously monitored, and, during the industrial-scale tests, the toxic emissions (polychlorinated dibenzodioxins and dibenzofurans and heavy metals) were determined. Ash samples were analyzed for heavy metals in an inductively coupled plasma-atomic emission spectroscopy spectrophotometer. Problems were observed during the preparation of wastewood, because species embedded with different compounds, such as railway sleepers and demolition wood, were not easily treated. All wastewood blends were proven good fuels; co-combustion proceeded smoothly and homogeneous temperature and pressure profiles were obtained. Although some fluctuations were observed, low emissions of gaseous pollutants were obtained for all fuel blends. The metal element emissions (in the flue gases and the solid residues) were lower than the legislative limits. Therefore, wastewood co-combustion with lignite can be realized, provided that the fuel handling and preparation can be practically performed in large-scale installations.

Diatremes of the Hopi Buttes, Arizona; chemical and statistical analyses

USGS Publications Warehouse

Wenrich, K.J.; Mascarenas, J.F.

1982-01-01

Lacustrine sediments deposited in maar lakes of the Hopi Buttes diatremes are hosts for uranium mineralization of as much as 1500 ppm. The monchiquites and limburgite turfs erupted from the diatremes are distinguished from normal alkalic basalts of the Colorado Plateau by their extreme silica undersaturation and high water, TiO2, and P2O5 contents. Many trace elements are also unusually abundant, including Ag, As, Ba, Be, Ce, Dy, Eu, F, Gd, Hf, La, Nd, Pb, Rb, Se, Sm, Sn, Sr, Ta, Tb, Th, U, V, Zn, and Zr. The lacustrine sediments, which consist predominantly of travertine and clastic rocks, are the hosts for syngenetic and epigenetic uranium mineralization of as much as 1500 ppm uranium. Fission track maps show the uranium to be disseminated within the travertine and clastic rocks, and although microprobe analyses have not, as yet, revealed discrete uranium-bearing phases, the clastic rocks show a correlation of high Fe, Ti, and P with areas of high U. Correlation coefficients show that for the travertines, clastics, and limburgite ruffs, Mo, As, Sr, Co, and V appear to have the most consistent and strongest correlations with uranium. Many elements, including many of the rare-earth elements, that are high in these three rocks are also high in the monchiquites, as compared to the average crustal abundance for the respective rock type. This similar suite of anomalous elements, which includes such immobile elements as the rare earths, suggests that Fluids which deposited the travertines were related to the monchiquitic magma. The similar age of about 5 m.y. for both the lake beds and the monchiquites also appears to support this source for the mineralizing fluids.

Uranium-238 and thorium-232 series concentrations in soil, radon-222 indoor and drinking water concentrations and dose assessment in the city of Aldama, Chihuahua, Mexico.

PubMed

Colmenero Sujo, L; Montero Cabrera, M E; Villalba, L; Rentería Villalobos, M; Torres Moye, E; García León, M; García-Tenorio, R; Mireles García, F; Herrera Peraza, E F; Sánchez Aroche, D

2004-01-01

High-resolution gamma spectrometry was used to determine the concentration of 40K, 238U and 232Th series in soil samples taken from areas surrounding the city of Aldama, in Chihuahua. Results of indoor air short-time sampling, with diffusion barrier charcoal detectors, revealed relatively high indoor radon levels, ranging from 29 to 422 Bq/m3; the radon concentrations detected exceeded 148 Bq/m3 in 76% of the homes tested. Additionally, liquid scintillation counting showed concentrations of radon in drinking water ranging from 4.3 to 42 kBq/m3. The high activity of 238U in soil found in some places may be a result of the uranium milling process performed 20 years ago in the area. High radon concentrations indoor and in water may be explained by assuming the presence of uranium-bearing rocks underneath of the city, similar to a felsic dike located near Aldama. The estimated annual effective dose of gamma radiation from the soil and radon inhalation was 3.83 mSv.

Evaluation of mine fires due to spontaneous combustion in the mechanized faces of Middle Anatolian Lignite mine (OAL), case studies

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

Gueyagueler, T.; Karaman, H.

1995-12-31

In this paper fires due to spontaneous combustion in Middle Anatolian Lignite mine (OAL) which is the first fully mechanized underground lignite mine in Turkey, are studied. Since the installation of mechanization, due to spontaneous heating, four panel fires namely, AO1, AO2, AO3 and AO4 have broken out. During these fires, the concentrations of carbon monoxide, methane and the velocity of air are measured continuously by the Micro Minos Environmental monitoring system. For each fire, the environment where fire has started is examined and the possible causes of the fire are investigated. Also the precautions taken to extinguish the firemore » at different stages are described and the importance of the early detection of mine fire are discussed together with the limitations of the monitoring system the practical difficulties observed during the fire.« less

The effect of the depth and groundwater on the formation of sinkholes or ground subsidence associated with abandoned room and pillar lignite mines under static and dynamic conditions

NASA Astrophysics Data System (ADS)

Aydan, Ö.; Ito, T.

2015-11-01

It is well known that some sinkholes or subsidence take place from time to time in the areas where abandoned room and pillar type mines exist. The author has been involved with the stability of abandoned mines beneath urbanized residential areas in Tokai region and there is a great concern about the stability of these abandoned mines during large earthquakes as well as in the long term. The 2003 Miyagi Hokubu and 2011 Great East Japan earthquakes caused great damage to abandoned mines and resulted in many collapses. The author presents the effect of the depth and groundwater on the formation of sinkholes or ground subsidence associated with abandoned room and pillar lignite mines under static and dynamic conditions and discusses the implications on the areas above abandoned lignite mines in this paper.

Production of a nitrogeneous humic fertilizer by the oxidation-ammoniation of lignite

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

Coca, J.

1984-12-01

Two lignite samples were oxidised with HNO/sub 3/ (20% wt) at 75 C and treated afterwards with NH/sub 3/ in a fluidised-bed reactor in a temperature range 100-375 C. The effects of temperature, NH/sub 3/ flow rate, and reaction time on the total N/sub 2/ content of the product are reported. The product contained 7-13% wt of total N/sub 2/ which increased as the ammoniation temperature increased. Soil nitrification measurements of the N/sub 2/-enriched lignites showed that the maximum conversion to nitrates and rate of nitrification are exhibited by the product obtained at the lowest ammoniation temperature, i.e. 100 C.more » Maximum conversion to nitrates at that temperature was 45%, which compares well with similar products such as ammoniated peat (35%) and ammonium nitrohumates (45%).« less

Quantification of kinetic rate law parameters for the dissolution of natural autunite in the presence of aqueous bicarbonate ions at high concentrations

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

Gudavalli, Ravi; Katsenovich, Yelena; Wellman, Dawn

Uranium is a key contaminant of concern in the groundwater at 91 waste sites at 18 U.S. Department of Energy (DOE) facilities within the United States and is a potential source of groundwater contamination and a risk to human health and the environment through discharges to surface water. Dissolved inorganic carbon (bicarbonate/carbonate) has a high affinity for complexing with uranium that is present as sorbed or unique uranium-bearing mineral phases within the sedimentary matrix. This process can result in the formation of soluble uranyl carbonate aqueous species, which are mobile under circumneutral pH conditions. This study was conducted to quantifymore » the rate of release of uranium from the autunite mineral, (Ca[(UO 2)(PO 4)] 2∙3H 2O), that was formed during polyphosphate injection to remediate uranium; the dissolution of uranium was studied as a function of the aqueous bicarbonate concentration, ranging from 25 to 100 mM. Experiments were carried out in the pH range from 7 to 11 in the temperature range of 23-90°C via single-pass flow-through testing. Consistent with the results of previous studies (Gudavalli et al., 2013 a, b), the rate of uranium release from autunite exhibited minimal dependency on temperature, but was strongly dependent on pH and increasing concentrations of bicarbonate in the solution. Data obtained during these experiments were compared with results of previous experiments conducted using a low-concentration range of bicarbonate solutions (0.5-3.0 mM). An 8- to 30 fold increase in the rate of uranium release was observed in the presence of high bicarbonate concentrations at pH 7-8 compared to low bicarbonate values, while at pH 9-11, there was only a 5-fold increase in uranium rate of release with an increase in bicarbonate concentrations. The rate of uranium release was calculated to be between 5.18 x 10 -8 and 1.69 x 10 -7 mol m -2 s -1. The activation energy values at high and low bicarbonate concentrations were similar, with ratio values in the range of 0.6-1.0.« less

Quantification of kinetic rate law parameters for the dissolution of natural autunite in the presence of aqueous bicarbonate ions at high concentrations.

PubMed

Gudavalli, Ravi; Katsenovich, Yelena; Wellman, Dawn

2018-05-02

Uranium is a key contaminant of concern in the groundwater at U.S. Department of Energy (DOE) facilities within the United States and is a potential source of groundwater contamination and a risk to human health and the environment through discharges to surface water. Dissolved inorganic carbon (bicarbonate/carbonate) has a high affinity for complexing with uranium that is present as sorbed or unique uranium-bearing mineral phases within the sedimentary matrix. This process can result in the formation of soluble uranyl carbonate aqueous species, which are mobile under circumneutral pH conditions. This study was conducted to quantify the rate of release of uranium from the autunite mineral, (Ca[(UO 2 )(PO 4 )] 2 •3H 2 O), that was formed during polyphosphate injection to remediate uranium; the dissolution of uranium was studied as a function of the aqueous bicarbonate concentration, ranging from 25 to 100 mM. Experiments were carried out in the pH range from 7 to 11 in the temperature range of 23-90 °C via single-pass flow-through testing. Consistent with the results of previous studies (Gudavalli et al., 2013a, 2013b), the rate of uranium release from autunite exhibited minimal dependency on temperature, but was strongly dependent on pH and increasing concentrations of bicarbonate in the solution. Data obtained during these experiments were compared with results of previous experiments conducted using a low-concentration range of bicarbonate solutions (0.5-3.0 mM). An 8- to 30-fold increase in the rate of uranium release was observed in the presence of high bicarbonate concentrations at pH 7-8 compared to low bicarbonate values, while at pH 9-11, there was only a 5-fold increase in uranium rate of release with an increase in bicarbonate concentrations. The rate of uranium release was calculated to be between 5.18 × 10 -8 and 1.69 × 10 -7  mol m -2 s -1 . The activation energy values at high and low bicarbonate concentrations were similar, with ratio values in the range of 0.6-1.0. Copyright © 2018 Elsevier Ltd. All rights reserved.

Results of exploration at the Old Leyden coal mine, Jefferson County, Colorado

USGS Publications Warehouse

Gude, A.J.; McKeown, F.A.

1953-01-01

Six diamond core holes totaling 2, 201 feet were drilled by the. U, S. Bureau of Mines under contract to the U. S. Atomic Energy Commission at the Old Leyden coal mine, Jefferson County, Colo. The holes were spotted on the basis of geologic mapping by the U. S. Geological survey and were drilled to explore the lateral and downward extent of a uranium-bearing coal and the associated carnotite deposits in the adjacent sandstone° The data obtained from the diamond-core holes helped to explain the geology and structural control of the deposit. The uranium is most abundant in a coal bed that in places has been brecciated by shearing. and then altered to a hard, dense, and silicified rock. The uraniferous coal is in the nearly vertical beds of the Laramie formation of Upper Cretaceous age. Small lenticular bodies of uraniferous material, 50 feet long, 25 to 30 feet wide, and 2 to 4 feet thick, occur at intervals in the coal and silicified coal over a strike length of about 800 feet. These bodies contain 0.10 to 0.50 percent uranium. Data obtained from the drilling indicate a discontinuous radioactive zone between these higher-grade bodies; assays of samples from the cores range from 0.001 to 0.10 percent uranium. All drill holes were probed by Survey and A. E. C. logging equipment and showed anomalies where the core assayed more than 0.005 percent uranium. Material of ore grade--0.10 percent uranium--was found in one core; the rock in the other five holes was of lower grade. The presence of the radioactive zone in all holes suggests, however, that uranium is distributed irregularly in a southerly plunging deposit which is exposed in the adit, on the outcrop, and in other diamond-drill holes that were put down by the lessee.

Assessment of natural radioactivity in aquifer medium bearing uranium ores in Koprubasi, Turkey

NASA Astrophysics Data System (ADS)

Simsek, Celalettin

2008-10-01

Koprubasi, located within Manisa Province near the Izmir, is the biggest uranium mine where uranium ores originate from Neogene aged altered sandstone and conglomerate layers. The main objective of this study is to determine the radiation hazard associated with radioactivity levels of uranium ores, and the rocks and sediments around Koprubasi. In this regard, measured activity levels of 226Ra, 232Th and 40K were compared with world averages. The average activity levels of 226 Ra, 232Th and 40K were measured to be 5369.75, 124.78 and 10.0 Bq/kg in uranium ores, 24.32, 52.94 and 623.38 Bq/kg in gneiss, 46.24, 45.13 and 762.26 Bq/kg in sandstone and conglomerate, 73.11, 43.15 and 810.65 Bq/kg in sediments, respectively. All samples have high 226Ra and 40K levels according to world average level. As these sediments are used as construction materials and in agricultural activities within the study area, the radiation hazard are calculated by using dose rate (D), annual effective dose rate (He), radium equivalent activity (Raeq) and radiation hazard index (Iyr). All the samples have Raeq levels that are lower than the world average limit of 370 Bq/kg. On the other hand, D, He and Iyr values are higher than world average values. These results indicate that the uranium ores in the Koprubasi is the most important contributor to the natural radiation level. The radioactivity levels of sediments and rocks make them unsuitable for use as agricultural soil and as construction materials. Moreover, it is determined that shallow groundwater in sediments and deep groundwater in conglomerate rocks and also surface water sources in the Koprubasi have high 226Ra content. According to environmental radioactive baseline, some environmental protection study must be taken in Koprubasi uranium site and the environment.

Uranium speciation in acid waste-weathered sediments: The role of aging and phosphate amendments

DOE PAGES

Perdrial, Nicolas; Vázquez-Ortega, Angélica; Wang, Guohui; ...

2017-12-05

Uranium speciation and lability are strongly coupled to mineral transformations in silicate sediments, particularly for sediments subjected to weathering in acidic, high-level radioactive waste, as occurred at the Department of Energy's Hanford (WA) site. Here, uncontaminated Hanford sediments were reacted for 365 days with acidic (pH 3), uranium-bearing waste solutions, with and without phosphate in batch experiments, prior to detailed characterizations using electron microscopy, x-ray diffraction and x-ray absorption spectroscopy. In PO 4-reactant free systems, uranium speciation was controlled initially by precipitation of compreignacite [K 2(UO 2) 6O 4(OH) 6·8H 2O]- and becquerelite [Ca(UO 2) 6O 4(OH) 6·8H 2O]-like species.more » Subsequent further removal of uranium coincided with that of Si and accumulation of boltwoodite, [(K, Na)(UO 2) 2O 4(HSiO 4) 2•0.5(H 2O)]-like species of uranium at 180 and 365 days. When present, PO 4 exerted a direct and strong control over U speciation. Furthermore, the detection of meta-ankoleite, [K 2(UO 2) 2O 4(PO 4) 2·6H 2O] at all reaction times when U was present emphasizes the importance of dissolved phosphate as a control on U speciation. Here, meta-ankoleite appears well crystallized and when it occurs as the principal product of sediment weathering, its low solubility is expected to limit dissolved U(VI) concentrations in groundwater. Although boltwoodite solubility is also low, it is formed more slowly (and only when PO 4 is absent), after initial precipitation of more soluble, less crystalline uranyl hydroxides. In the context of Hanford crib waste our results suggest that with PO 4 present, nearly all uranium would have precipitated in the upper soil.« less

Uranium speciation in acid waste-weathered sediments: The role of aging and phosphate amendments

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

Perdrial, Nicolas; Vázquez-Ortega, Angélica; Wang, Guohui

Uranium speciation and lability are strongly coupled to mineral transformations in silicate sediments, particularly for sediments subjected to weathering in acidic, high-level radioactive waste, as occurred at the Department of Energy's Hanford (WA) site. In this study, uncontaminated Hanford sediments were reacted for 365 days with acidic (pH 3), uranium-bearing waste solutions, with and without phosphate in batch experiments, prior to detailed characterizations using electron microscopy, x-ray diffraction and x-ray absorption spectroscopy. In PO(4)(-)reactant free systems, uranium speciation was controlled initially by precipitation of compreignacite [K-2(UO2)(6)O-4(OH)(6)center dot 8H(2)O]-and becquerelite [Ca(UO2)(6)O-4(OH)(6)center dot 8H(2)O]-like species. Subsequent further removal of uranium coincided withmore » that of Si and accumulation of boltwoodite, [(K, Na)(UO2)(2)O-4(HSiO4)(2)center dot 0.5(H2O)]-like species of uranium at 180 and 365 days. When present, PO4 exerted a direct and strong control over U speciation. The detection of meta-ankoleite, [K-2(UO2)(2)O-4(PO4)(2)center dot 6H(2)O] at all reaction times when U was present emphasizes the importance of dissolved phosphate as a control on U speciation. Here, meta-ankoleite appears well crystallized and when it occurs as the principal product of sediment weathering, its low solubility is expected to limit dissolved U(VI) concentrations in groundwater. Although boltwoodite solubility is also low, it is formed more slowly (and only when PO4 is absent), after initial precipitation of more soluble, less crystalline uranyl hydroxides. In the context of Hanford crib waste our results suggest that with PO4 present, nearly all uranium would have precipitated in the upper soil.« less

Uranium speciation in acid waste-weathered sediments: The role of aging and phosphate amendments

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

Perdrial, Nicolas; Vázquez-Ortega, Angélica; Wang, Guohui

Uranium speciation and lability are strongly coupled to mineral transformations in silicate sediments, particularly for sediments subjected to weathering in acidic, high-level radioactive waste, as occurred at the Department of Energy's Hanford (WA) site. Here, uncontaminated Hanford sediments were reacted for 365 days with acidic (pH 3), uranium-bearing waste solutions, with and without phosphate in batch experiments, prior to detailed characterizations using electron microscopy, x-ray diffraction and x-ray absorption spectroscopy. In PO 4-reactant free systems, uranium speciation was controlled initially by precipitation of compreignacite [K 2(UO 2) 6O 4(OH) 6·8H 2O]- and becquerelite [Ca(UO 2) 6O 4(OH) 6·8H 2O]-like species.more » Subsequent further removal of uranium coincided with that of Si and accumulation of boltwoodite, [(K, Na)(UO 2) 2O 4(HSiO 4) 2•0.5(H 2O)]-like species of uranium at 180 and 365 days. When present, PO 4 exerted a direct and strong control over U speciation. Furthermore, the detection of meta-ankoleite, [K 2(UO 2) 2O 4(PO 4) 2·6H 2O] at all reaction times when U was present emphasizes the importance of dissolved phosphate as a control on U speciation. Here, meta-ankoleite appears well crystallized and when it occurs as the principal product of sediment weathering, its low solubility is expected to limit dissolved U(VI) concentrations in groundwater. Although boltwoodite solubility is also low, it is formed more slowly (and only when PO 4 is absent), after initial precipitation of more soluble, less crystalline uranyl hydroxides. In the context of Hanford crib waste our results suggest that with PO 4 present, nearly all uranium would have precipitated in the upper soil.« less

Petrological, geochemical and isotopic characteristics of lignite and calcified lignite from mining area Pesje, Velenje Basin, Slovenia

NASA Astrophysics Data System (ADS)

Vrabec, Mirijam; Markič, Miloš; Vrabec, Marko; Jaćimović, Radojko; Kanduč, Tjaša

2014-05-01

Lignite (organic rich) and calcified lignite (inorganic rich) samples from excavation field -50c mining area Pesje, Velenje Basin, Slovenia were investigated. During geological and structural mapping lignite and calcified lignite samples were systematically taken for determination of their petrological, geochemical and isotopic characteristics. Lignite is composed of fine detritical gelified matrix. At least five different types of calcified lignite were recognized forming laminations, calcifications after wood, petrified wood and complete replacements of lignite with carbonate. All measured parameters so far indicate geochemical processes during sedimentation of the Velenej Basin. After macroscopic description samples were split to organic and inorganic component (Ward, 1984) and powdered in an agate mortar for geochemical and isotopic analyses. Major and trace elements (As, B, Ba, Cd, Co, Cr, Cu, Hg, Mn, Mo, Sb, Se, Th, U, Zn) in these samples were determined by instrumental neutron activation analysis (INAA) using k-0 standardization method (Jaćimović et al, 2002). The isotopic composition of carbon and nitrogen was determined using a Europa 20-20 continuous flow IRMS ANCA-SL preparation module. A 1 mg amount of a sample was weighed in a tin capsule for carbon and 10 mg for nitrogen analysis. Samples for carbon analyses were pretreated with 1 M HCl to remove carbonates. Carbonate samples from carbonate-rich strata and calcified xylite were first roasted at 450 deg C (Krantz et al., 1987). Three miligrams of carbonate sample was transformed into CO2 by reaction with anhydrous H3PO4 at 55 deg C under vacuum (McCrea, 1950) and measured with GV 2003 isotope ratio mass spectrometer. Measured isotopic composition of oxygen as VPDB values was recalculated to the VSMOW reference standard to enable the comparison with data from other coal basins. SEM/EDXS of carbonate rich sediments was performed with JEOL JSM 5800 electron microanalyzer scanning electron microscope energy dispersive X-ray spectroscopy at the Department of Ceramics at the Jožef Stefan Institute. Geochemical characteristics of major and trace elements indicate that the values of major and trace elements are comparable to world average coal (Zhang et al., 2004). Isotopic composition of carbon and isotopic composition of nitrogen of investigated samples indicate values from to -29.4o to -23.7o and 1.8o to 5.9o respectively. Lower value of isotopic composition of carbon indicates higher gelification (values up to -29.4) and higher value of isotopic composition of nitrogen (values up to 5.9) indicate higher mineralization. The results of SEM/EDXS microscopy revealed that in calcified lignite chemical composition of calcite prevails. Traces of diagenetic pyrite were also found, indicating localized anoxic conditions during sedimentation. Values of isotopic composition of CCaCO3 range from -2 to +13 and indicate temperature of precipitation from 17.3 to 35 deg C, which is similar to results obtained in previous studies (Kanduč et al., 2012). References Krantz, D.E., Williams, D.F., Jones, D.S., 1987: Ecological and paleoenvironmental information using stable isotope profiles from living and fossil mollusks. Palaeogeography, Palaeoclimatology, Palaeoecology 58, 249-266. Kanduč T., Markič M., Zavšek S., McIntosh J. 2012: carbon cycling in the Pliocene Velenje Coal Basin, Slovenia, inferred from stable carbon isotopes. International Journal of Coal Geology 89, 70-83. Jaćimović, R., Lazaru, A., Mihajlović, D., Ilić, R., Stafilov, T., 2002: Determination of major and trace elements in some minerals by k0-instrumental neutron activation analysis. Journal of Radioanalytical Nuclear Chemistry, 253, 427-434. McCrea, JM., 1950. On the isotopic chemistry of carbonates and a paleotemperature scale. Journal of Chemical Physics 18, 849. Ward C.R. (Ed.), 1984: Coal Geology and Coal Technology. Black-well, Oxford, 345 pp. Zhang J.Y., Zheng C.G., Ren D.Y., Chou C.L., Zheng R.S., Wang Z.P., Zhao F. H., Ge Y.T. 2004: Distribution of potentially hazardous trace elements in coals from Shoxi provinces, China. Fuel 83: 129-135.

Active methods of mercury removal from flue gases.

PubMed

Marczak, Marta; Budzyń, Stanisław; Szczurowski, Jakub; Kogut, Krzysztof; Burmistrz, Piotr

2018-03-23

Due to its adverse impact on health, as well as its global distribution, long atmospheric lifetime and propensity for deposition in the aquatic environment and in living tissue, the US Environmental Protection Agency (US EPA) has classified mercury and its compounds as a severe air quality threat. Such widespread presence of mercury in the environment originates from both natural and anthropogenic sources. Global anthropogenic emission of mercury is evaluated at 2000 Mg year -1 . According to the National Centre for Emissions Management (Pol. KOBiZE) report for 2014, Polish annual mercury emissions amount to approximately 10 Mg. Over 90% of mercury emissions in Poland originate from combustion of coal.The purpose of this paper was to understand mercury behaviour during sub-bituminous coal and lignite combustion for flue gas purification in terms of reduction of emissions by active methods. The average mercury content in Polish sub-bituminous coal and lignite was 103.7 and 443.5 μg kg -1 . The concentration of mercury in flue gases emitted into the atmosphere was 5.3 μg m -3 for sub-bituminous coal and 17.5 μg m -3 for lignite. The study analysed six low-cost sorbents with the average achieved efficiency of mercury removal from 30.6 to 92.9% for sub-bituminous coal and 22.8 to 80.3% for lignite combustion. Also, the effect of coke dust grain size was examined for mercury sorptive properties. The fine fraction of coke dust (CD) adsorbed within 243-277 μg Hg kg -1 , while the largest fraction at only 95 μg Hg kg -1 . The CD fraction < 0.063 mm removed almost 92% of mercury during coal combustion, so the concentration of mercury in flue gas decreased from 5.3 to 0.4 μg Hg m -3 . The same fraction of CD had removed 93% of mercury from lignite flue gas by reducing the concentration of mercury in the flow from 17.6 to 1.2 μg Hg m -3 . The publication also presents the impact of photochemical oxidation of mercury on the effectiveness of Hg vapour removal during combustion of lignite. After physical oxidation of Hg in the flue gas, its effectiveness has increased twofold.

Formation of albitite-hosted uranium within IOCG systems: the Southern Breccia, Great Bear magmatic zone, Northwest Territories, Canada

NASA Astrophysics Data System (ADS)

Montreuil, Jean-François; Corriveau, Louise; Potter, Eric G.

2015-03-01

Uranium and polymetallic U mineralization hosted within brecciated albitites occurs one kilometer south of the magnetite-rich Au-Co-Bi-Cu NICO deposit in the southern Great Bear magmatic zone (GBMZ), Canada. Concentrations up to 1 wt% U are distributed throughout a 3 by 0.5 km albitization corridor defined as the Southern Breccia zone. Two distinct U mineralization events are observed. Primary uraninite precipitated with or without pyrite-chalcopyrite ± molybdenite within magnetite-ilmenite-biotite-K-feldspar-altered breccias during high-temperature potassic-iron alteration. Subsequently, pitchblende precipitated in earthy hematite-specular hematite-chlorite veins associated with a low-temperature iron-magnesium alteration. The uraninite-bearing mineralization postdates sodic (albite) and more localized high-temperature potassic-iron (biotite-magnetite ± K-feldspar) alteration yet predates potassic (K-feldspar), boron (tourmaline) and potassic-iron-magnesium (hematite ± K-feldspar ± chlorite) alteration. The Southern Breccia zone shares attributes of the Valhalla (Australia) and Lagoa Real (Brazil) albitite-hosted U deposits but contains greater iron oxide contents and lower contents of riebeckite and carbonates. Potassium, Ni, and Th are also enriched whereas Zr and Sr are depleted with respect to the aforementioned albitite-hosted U deposits. Field relationships, geochemical signatures and available U-Pb dates on pre-, syn- and post-mineralization intrusions place the development of the Southern Breccia and the NICO deposit as part of a single iron oxide alkali-altered (IOAA) system. In addition, this case example illustrates that albitite-hosted U deposits can form in albitization zones that predate base and precious metal ore zones in a single IOAA system and become traps for U and multiple metals once the tectonic regime favors fluid mixing and oxidation-reduction reactions.

Radiometric reconnaissance in the Garfield and Taylor park quadrangles, Chaffee and Gunnison counties, Colorado

USGS Publications Warehouse

Dings, M.G.; Schafer, Max

1953-01-01

During the summer of 1952 most of the mines and prospects in the Garfield and Taylor Park quadrangles of west-central Colorado were examined radiometrically by the U. S. Geological Survey to determine the extent, grade, and mode of occurrence of radioactive substances. The region contains a relatively large number of rock types, chiefly pre-Cambrian schists, gneisses, and granites; large and small isolated areas of sedimentary rocks of Paleozoic and Mesozoic ages; and a great succession of intrusive rocks of Tertiary age that range from andesite to granite and occur as stocks, chonoliths, sills, dikes, and one batholith. The prevailing structures are northwest-trending folds and faults. Ores valued at about $30,000,000 have been produced from this region. Silver, lead, zinc, and gold have accounted for most of this value, but small tonnages of copper, tungsten, and molybdenum have also been produced. The principal ore minerals are sphalerite, silver-bearing galena, cerussite, smithsonite, and gold-bearing pyrite and limonite; they occur chiefly as replacement bodies in limestone and as shoots in pyritic quartz veins. Anomalous radioactivity is uncommon and the four localities at which it is known are widely separated in space. The uranium content of samples from these localities is low. Brannerite, the only uranium-bearing mineral positively identified in the region, occurs sparingly in a few pegmatites and in one quartz-beryl-pyrite vein. Elsewhere radioactivity is associated with (l) black shale seams in the Manitou dolomite, (2) a quartz-pyrite-molybdenite vein, (3) a narrow border zone of oxidized material surrounding a small lead zinc ore body in the Manitou dolomite along a strong fault zone.

Final Environmental Assessment for Proposed Construction II, Buckley Air Force Base, Colorado

DTIC Science & Technology

2004-06-01

Onopordum acanthium Scotch thistle Salsola sp. Russian thistle Tamarisk ramosissima Saltcedar Verbascum thapsus Mullein 3.7.4 Site-Specific...AFB by the City of Aurora. 3.10 RADON Radon is an odorless, tasteless radioactive gas. It is released by the breakdown of uranium -bearing deposits...such as sterile oats or winter wheat to establish root mass and compete with weeds • Follow sterile oats or winter wheat planting with mixed grass

Desulphurization of coal using borax

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

Yaman, S.; Kuecuekbayrak, S.

1996-12-31

In this study, a high sulphur Turkish lignite was mixed with various amounts of solid borax [Na{sub 2}B{sub 4}O{sub 7}10H{sub 2}O] and then these mixtures were subjected to various oxydesulphurization processes. Effects of amount of borax, temperature and partial pressure of oxygen on sulphur removal and coal recovery were investigated in the ranges of 0.625--15.000 g for 5 g lignite, 423--498 K, 0.0--1.5 MPa, respectively.

Mineralogical composition of boiler fouling and slagging deposits and their relation to fly ashes: the case of Kardia power plant.

PubMed

Kostakis, George

2011-01-30

Slagging and fouling deposits from a pulverized lignite fired steam generating unit of the Kardia power plant (West Macedonia, Greece) were mineralogically investigated. The structure and cohesion of these deposits varied, usually depending on the level height of the boiler unit where they were formed. Some of the deposits had complex phase composition. The dominant components of the deposits of the burner zone and of the lower and intermediate boiler zones were the amorphous, anhydrite and hematite, while those of the highest levels contained amorphous, and anhydrite. Furthermore, in deposits formed in various other boiler areas gehlenite, anorthite, diopside, quartz, Ca(2)SiO(4), brownmillerite and other crystalline phases were also identified, usually in low amounts or in traces. The major part of the phases constituting the deposits were formed in the boiler, since only a minor part derived from the unreacted minerals present in lignite. Anhydrite was generated from the reaction of SO(2) with CaO formed mainly by the calcination of calcite as well as from dehydration of gypsum contained in lignite, while hematite was produced mainly from the oxidation of pyrite. The calcium-containing silicates formed in the boiler were mainly the products of reactions between CaO and minerals contained in the lignite. Copyright © 2010 Elsevier B.V. All rights reserved.

Coal industry of Turkey

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

Cetincelik, M.

1979-09-01

The known occurrences of hard (bituminous) coal in Turkey are very limited. Total resources are estimated to be 1,500,000,000 metric tons of which 205,000,000 tons are considered to be technically and economically recoverable at the present time. Tertiary lignite deposits are found extensively throughout Turkey. Total resources of lignite are estimated to be about 5,140,000,000 metric tons of which 2,740,000,000 tons are considered to be recoverable. In 1978, Turkey completely nationalized its coal industry whereby the government was authorized to take over all private mines. As a result of this, a major increase in coal production is expected based onmore » a new energy policy. Turkish Coal Enterprises (TKI), a state-owned organization, is now in control of the entire coal industry. TKI was established by law in 1957 and has its headquarters in Ankara. The gradually changing structure of Turkey's national economy from agriculture to increased industrialization has been accompanied by a rise in energy requirements. However, the lack of recent industrial expansion and the decline in the national economy has been due to the shortage of energy. A new energy plan developed for the country has established that, in the future, lignite will be used in far greater proportions for electricity generation (burned in captive plants). The nationalization of Turkey's lignite mines is expected to ensure a coordinated and effective means of meeting the demand.« less

Advanced power assessment for Czech lignite. Task 3.6, Volume 1

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

Sondreal, E.A.; Mann, M.D.; Weber, G.W.

1995-12-01

The US has invested heavily in research, development, and demonstration of efficient and environmentally acceptable technologies for the use of coal. The US has the opportunity to use its leadership position to market a range of advanced coal-based technologies internationally. For example, coal mining output in the Czech Republic has been decreasing. This decrease in demand can be attributed mainly to the changing structure of the Czech economy and to environmental constraints. The continued production of energy from indigenous brown coals is a major concern for the Czech Republic. The strong desire to continue to use this resource is amore » challenge. The Energy and Environmental Research Center undertook two major efforts recently. One effort involved an assessment of opportunities for commercialization of US coal technologies in the Czech Republic. This report is the result of that effort. The technology assessment focused on the utilization of Czech brown coals. These coals are high in ash and sulfur, and the information presented in this report focuses on the utilization of these brown coals in an economically and environmentally friendly manner. Sections 3--5 present options for utilizing the as-mined coal, while Sections 6 and 7 present options for upgrading and generating alternative uses for the lignite. Contents include Czech Republic national energy perspectives; powering; emissions control; advanced power generation systems; assessment of lignite-upgrading technologies; and alternative markets for lignite.« less

Sorption of the monoterpenes α-pinene and limonene to carbonaceous geosorbents including biochar.

PubMed

Hale, Sarah E; Endo, Satoshi; Arp, Hans Peter H; Zimmerman, Andrew R; Cornelissen, Gerard

2015-01-01

The sorption of two monoterpenes, α pinene and limonene to the carbonaceous geosorbents graphite, bituminous coal, lignite coke, biochar and Pahokee peat was quantified. Polyethylene (PE) passive samplers were calibrated for the first time for these compounds by determining the PE-water partitioning coefficients and used as a tool to determine sorption to the carbonaceous geosorbents. Log KPE-water values were 3.49±0.58 for α pinene and 4.08±0.27 for limonene. The sorption of limonene to all materials was stronger than that for α pinene (differences of 0.2-1.3 log units between distribution coefficients for the monoterpenes). Placing Kd values in increasing order for α pinene gave biochar≈Pahokee peat≈bituminous coal≈lignite coke

Origin of coffinite in sedimentary rocks by a sequential adsorption-reduction mechanism.

USGS Publications Warehouse

Goldhaber, M.B.; Hemingway, B.S.; Mohagheghi, A.; Reynolds, R.L.; Northrop, H.R.

1987-01-01

Coffinite is the dominant ore mineral in the V-U ores of the Tony-M mine in the Henry Mts mineral belt of the Colorado Plateau. This orebody was formed at a density-stratified solution interface between uranyl-ion-bearing meteoric water and a saline fluid which was locally reducing. The localization of U at this solution interface occurred by adsorption onto the surfaces of detrital minerals, this adsorption being related to the pH difference between the two fluids. Experimental evidence is presented showing that the adsorption facilitated the reduction of uranium to U(IV). This adsorbed, reduced uranium bonded with aqueous silica in the ore zone to form coffinite. The high concentration of silica (as a monomeric species) in the ore-forming solution stabilized coffinite in preference to uraninite.-R.A.H.

Forms of uranium associated to silica in the environment of the Nopal deposit (Mexico)

NASA Astrophysics Data System (ADS)

Allard, T.; Othmane, G.; Menguy, N.; Vercouter, T.; Morin, G.; Calas, G.; Fayek, M.

2011-12-01

The understanding of the processes that control the transfers of uranium in the environment is necessary for the safety assessement of nuclear waste repositories. In particular, several poorly ordered phases (e.g. Fe oxihydroxides) are expected to play an important role in trapping uranium from surface waters. Among them, natural systems containing amorphous silica are poorly documented. A former study from the environment of the Peny mine (France) showed the importance of silica in uranium speciation [1]. The Nopal uranium deposit is located in volcanic tuff from tertiary period. It hosted several hydrothermal alteration episodes responsible for clay minerals formation. A primary uranium mineralisation occurred in a breccia pipe, consisting in uraninite, subsequently altered in secondary uranium minerals among which several silicates. Eventually, opal was formed and coated uranyl silicates such as uranophane and weeksite [2], [3]. Opals also contain minor amounts of uranium. The Nopal deposit is still considered as a natural analogue of high level nuclear waste repository located in volcanic tuff. It may be used to reveal the low temperature conditions of trapping of uranium in systems devoid of iron oxides such as silica-containing ones. The aim of this study is then to determine the uranium speciation, and its possible complexity, associated to these opals that represent a late trapping episode. It will provide insights ranging from the micrometer scale of electron microscopies to the molecular scale provided by fluorescence spectroscopy. Three samples of green or yellow opals have been analysed by a combination of complementary tools including scanning electron microscopy (SEM) on cross-sections, transmission electron microscopy (TEM) on focused ion beam (FIB) films, cathodoluminescence and time-resolved laser fluorescence spectroscopy (TRLFS). Uranium speciation was found to be complex. We first evidence U-bearing microparticles of beta-uranophane Ca[(UO2)(SiO3OH)]2(H2O)5 and apatite Ca5(PO4)3(OH,Cl,F) containing minor amounts of uranium. Uranophane was formed prior to opal and coated by it. However the major part of uranium is concentrated in Ca-U-enriched zones with a Ca:U ratio of 1:1 and displaying botryoidal features. The exact nature of Ca-U species in these zones was not specified but TEM, cathodoluminescence and TRLFS analyses suggest the presence of Cam-(UO2)m-(O/OH/H2O)n complexes adsorbed or incorporated in opal. These results will be discussed in terms of chemical conditions that prevailed during U incorporation and compared to other known U-Si environmental systems, including the Peny system (France). [1] Allard, T. et al. (1999) Chem. Geol., 158, 81-103 [2] Calas, G. et al. (2008) Terra Nova, 20, 206-212. [3] Schindler, M. et al. (2010) Geochim. Cosmochim. Ac, 74, 187-202.

Influence of uranyl speciation and iron oxides on uranium biogeochemical redox reactions

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

Stewart, B.D.; Amos, R.T.; Nico, P.S.

2010-03-15

Uranium is a pollutant of concern to both human and ecosystem health. Uranium's redox state often dictates its partitioning between the aqueous- and solid-phases, and thus controls its dissolved concentration and, coupled with groundwater flow, its migration within the environment. In anaerobic environments, the more oxidized and mobile form of uranium (UO{sub 2}{sup 2+} and associated species) may be reduced, directly or indirectly, by microorganisms to U(IV) with subsequent precipitation of UO{sub 2}. However, various factors within soils and sediments may limit biological reduction of U(VI), inclusive of alterations in U(VI) speciation and competitive electron acceptors. Here we elucidate themore » impact of U(VI) speciation on the extent and rate of reduction with specific emphasis on speciation changes induced by dissolved Ca, and we examine the impact of Fe(III) (hydr)oxides (ferrihydrite, goethite and hematite) varying in free energies of formation on U reduction. The amount of uranium removed from solution during 100 h of incubation with S. putrefaciens was 77% with no Ca or ferrihydrite present but only 24% (with ferrihydrite) and 14% (no ferrihydrite) were removed for systems with 0.8 mM Ca. Imparting an important criterion on uranium reduction, goethite and hematite decrease the dissolved concentration of calcium through adsorption and thus tend to diminish the effect of calcium on uranium reduction. Dissimilatory reduction of Fe(III) and U(VI) can proceed through different enzyme pathways, even within a single organism, thus providing a potential second means by which Fe(III) bearing minerals may impact U(VI) reduction. We quantify rate coefficients for simultaneous dissimilatory reduction of Fe(III) and U(VI) in systems varying in Ca concentration (0 to 0.8 mM), and using a mathematical construct implemented with the reactive transport code MIN3P, we reveal the predominant influence of uranyl speciation, specifically the formation of uranyl-calcium-carbonato complexes, and ferrihydrite on the rate and extent of uranium reduction in complex geochemical systems.« less

Geology of the Midnite uranium mine, Stevens County, Washington; a preliminary report

USGS Publications Warehouse

Nash, J. Thomas; Lehrman, Norman J.

1975-01-01

The Midnite mine is one of only two mines in the United States currently producing uranium from discordant deposits in crystalline host rocks. Ore bodies are in metamorphosed steeply dipping Precambrian pelitic and calcareous rocks of a roof pendant adjacent to a Cretaceous(?) porphyritic quartz monzonite pluton. Production during 14 years, of operation has been about 8 million pounds of U3O8 from oxidized and reduced ores averaging 0.23 percent U3O8. Uranium deposits are generally tabular in form and dimensions range up to 380 m long, 210 m wide, and 50 m thick. Deposits are bounded on at least one side by unmineralized intrusive ribs of granitic rock, and thickest mineralized zones invariably occur at depressions in the intrusive contact. Upper limits of some deposits are nearly horizontal, and upper elevations of adjacent mineralized zones separated by ribs of granite are similar. Near surface ore is predominantly autunite, but ore at depth consists of pitchblende and coffinite with abundant pyrite and marcasite. Uranium minerals occur as .disseminations along foliation, replacements, and stockwork fracture-fillings. No stratigraphic controls on ore deposition are recognized. Rather, mineralized zones cut across lithologic boundaries if permeability is adequate. Most ore is in muscovite schist and mica phyllite, but important deposits occur in calc-silicate hornfels. Amphibolite sills and mid-Tertiary dacite dikes locally, carry ore where intensely fractured. High content of iron and sulfur, contained chiefly in FeS2, appear to be an important feature of favorable host rocks. Geometry of deposits, structural, and geochemical features suggest that uranium minerals were deposited over a span of time from late Cretaceous to late Tertiary. Ore occurs in but is not offset by a shear zone that displaces mid-Tertiary rocks.. Economic zones of uranium are interpreted to have been secondarily enriched in late Tertiary time by downward and lateral migration of uranium into permeable zones where deposition was influenced by ground water controls and minerals that could reduce or neutralize uranium-bearing solutions.

Actinide Oxidation State and O/M Ratio in Hypostoichiometric Uranium-Plutonium-Americium U0.750Pu0.246Am0.004O2-x Mixed Oxides.

PubMed

Vauchy, Romain; Belin, Renaud C; Robisson, Anne-Charlotte; Lebreton, Florent; Aufore, Laurence; Scheinost, Andreas C; Martin, Philippe M

2016-03-07

Innovative americium-bearing uranium-plutonium mixed oxides U1-yPuyO2-x are envisioned as nuclear fuel for sodium-cooled fast neutron reactors (SFRs). The oxygen-to-metal (O/M) ratio, directly related to the oxidation state of cations, affects many of the fuel properties. Thus, a thorough knowledge of its variation with the sintering conditions is essential. The aim of this work is to follow the oxidation state of uranium, plutonium, and americium, and so the O/M ratio, in U0.750Pu0.246Am0.004O2-x samples sintered for 4 h at 2023 K in various Ar + 5% H2 + z vpm H2O (z = ∼ 15, ∼ 90, and ∼ 200) gas mixtures. The O/M ratios were determined by gravimetry, XAS, and XRD and evidenced a partial oxidation of the samples at room temperature. Finally, by comparing XANES and EXAFS results to that of a previous study, we demonstrate that the presence of uranium does not influence the interactions between americium and plutonium and that the differences in the O/M ratio between the investigated conditions is controlled by the reduction of plutonium. We also discuss the role of the homogeneity of cation distribution, as determined by EPMA, on the mechanisms involved in the reduction process.

Impact of uranyl-calcium-carbonato complexes on uranium(VI) adsorption to synthetic and natural sediments

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

Stewart, B.D.; Mayes, Melanie; Fendorf, Scott

2010-01-01

Adsorption on soil and sediment solids may decrease aqueous uranium concentrations and limit its propensity for migration in natural and contaminated settings. Uranium adsorption will be controlled in large part by its aqueous speciation, with a particular dependence on the presence of dissolved calcium and carbonate. Here we quantify the impact of uranyl speciation on adsorption to both goethite and sediments from the Hanford Clastic Dike and Oak Ridge Melton Branch Ridgetop formations. Hanford sediments were preconditioned with sodium acetate and acetic acid to remove carbonate grains, and Ca and carbonate were reintroduced at defined levels to provide a rangemore » of aqueous uranyl species. U(VI) adsorption is directly linked to UO{sub 2}{sup 2+} speciation, with the extent of retention decreasing with formation of ternary uranyl-calcium-carbonato species. Adsorption isotherms under the conditions studied are linear, and K{sub d} values decrease from 48 to 17 L kg{sup -1} for goethite, from 64 to 29 L kg{sup -1} for Hanford sediments, and from 95 to 51 L kg{sup -1} for Melton Branch sediments as the Ca concentration increases from 0 to 1 mM at pH 7. Our observations reveal that, in carbonate-bearing waters, neutral to slightly acidic pH values ({approx}5) and limited dissolved calcium are optimal for uranium adsorption.« less

Leaching behavior of rare earth elements in fort union lignite coals of North America

DOE PAGES

Laudal, Daniel A.; Benson, Steven A.; Addleman, Raymond Shane; ...

2018-03-30

Fort Union lignite coal samples were subjected to a series of aqueous leaching experiments to understand the extraction behavior of the rare earth elements (REE). This testing was aimed at understanding the modes of occurrence of the REE in the lignite coals, as well as to provide foundational data for development of rare earth extraction processes. In a first series of tests, a sequential leaching process was used to investigate modes of occurrence of the REE of select lignite coals. The tests involved sequential exposure to solvents consisting of water, ammonium acetate and dilute hydrochloric acid (HCl). The results indicatedmore » that water and ammonium acetate extracted very little of the REE, indicating the REE are not present as water soluble or ion-exchangeable forms. However, the data shows that a large percentage of the REE were extracted with the hydrochloric acid (80–95 wt%), suggesting presence in HCl-soluble mineral forms such as carbonates, and/or presence as organic complexes. A second series of tests was performed involving single-step leaching with dilute acids and various operating parameters, including acid type, acid concentration, acid/coal contact time and coal particle size. For select samples, additional tests were performed to understand the results of leaching, including float-sink density separations and humic acid extraction. The results have shown that the majority of REE in Fort Union lignites appear to be associated weakly with the organic matrix of the coals, most likely as coordination complexes of carboxylic acid groups. The light REE and heavy REE exhibit different behaviors, however. The extractable light REE appear to have association both in acid-soluble mineral forms and as organic complexes, whereas the extractable heavy REE appear to be almost solely associated with the organics. In conclusion, scandium behavior was notably different than yttrium and the lanthanides, and the data suggests the extractable content is primarily associated as acid-soluble mineral forms.« less

Mid-latitude continental temperatures through the early Eocene in western Europe

NASA Astrophysics Data System (ADS)

Inglis, Gordon N.; Collinson, Margaret E.; Riegel, Walter; Wilde, Volker; Farnsworth, Alexander; Lunt, Daniel J.; Valdes, Paul; Robson, Brittany E.; Scott, Andrew C.; Lenz, Olaf K.; Naafs, B. David A.; Pancost, Richard D.

2017-02-01

Branched glycerol dialkyl glycerol tetraethers (brGDGTs) are increasingly used to reconstruct mean annual air temperature (MAAT) during the early Paleogene. However, the application of this proxy in coal deposits is limited and brGDGTs have only been detected in immature coals (i.e. lignites). Using samples recovered from Schöningen, Germany (∼48°N palaeolatitude), we provide the first detailed study into the occurrence and distribution of brGDGTs through a sequence of early Eocene lignites and associated interbeds. BrGDGTs are abundant and present in every sample. In comparison to modern studies, changes in vegetation type do not appear to significantly impact brGDGT distributions; however, there are subtle differences between lignites - representing peat-forming environments - and siliciclastic nearshore marine interbed depositional environments. Using the most recent brGDGT temperature calibration (MATmr) developed for soils, we generate the first continental temperature record from central-western continental Europe through the early Eocene. Lignite-derived MAAT estimates range from 23 to 26 °C while those derived from the nearshore marine interbeds exceed 20 °C. These estimates are consistent with other mid-latitude environments and model simulations, indicating enhanced mid-latitude, early Eocene warmth. In the basal part of the section studied, warming is recorded in both the lignites (∼2 °C) and nearshore marine interbeds (∼2-3 °C). This culminates in a long-term temperature maximum, likely including the Early Eocene Climatic Optimum (EECO). Although this long-term warming trend is relatively well established in the marine realm, it has rarely been shown in terrestrial settings. Using a suite of model simulations we show that the magnitude of warming at Schöningen is broadly consistent with a doubling of CO2, in agreement with late Paleocene and early Eocene pCO2 estimates.

Continental temperatures through the early Eocene in western central Europe

NASA Astrophysics Data System (ADS)

Inglis, G. N.; Collinson, M. E.; Riegel, W.; Wilde, V.; Farnsworth, A.; Lunt, D. J.; Robson, B.; Scott, A. C.; Lenz, O.; Pancost, R.

2016-12-01

In contrast to the marine realm, our understanding of terrestrial temperature change during greenhouse climates is poorly constrained. Recently, branched glycerol dialkyl glycerol tetraethers (brGDGTs) have been used to successfully reconstruct mean annual air temperature (MAAT) during the early Paleogene. However, despite the potential to provide new insights into terrestrial climate, the application of this proxy in lignite and coal deposits is still limited. Using samples recovered from Schöningen, Germany ( 48°N), we provide the first detailed study into the occurrence and distribution of brGDGTs through a sequence of Early Eocene lignites and associated marine interbeds. Branched GDGTs are abundant and present in every sample. In comparison to modern studies, changes in vegetation type do not appear to significantly impact brGDGT distributions; however, there are subtle differences in these distributions between lignites and siliciclastic nearshore marine interbed sediments. Using the most recent brGDGT temperature calibration, we generate the first continental temperature record from central-western continental Europe through the Early Eocene. Lignite-derived MAAT estimates range from 23 to 26°C and those derived from the nearshore marine interbeds always exceed 20°C. These estimates are consistent with other mid-latitude palaeoclimate proxy records which indicate enhanced early Eocene warmth. In the basal part of the section, warming is recorded in both the lignites ( 2°C) and nearshore marine interbeds ( 2-3°C). This culminates in a long-term temperature maximum, likely including the Early Eocene Climatic Optimum (EECO). Although this trend is relatively well established in marginal marine sediments within the SW Pacific, it has rarely been shown in other regions or terrestrial settings. Using a suite of new climate model simulations, our warming trend is consistent with a doubling of CO2 (from 560ppmv to 1120ppmv) which broadly agrees with proxy-derived CO2 estimates from the early Paleogene

Leaching behavior of rare earth elements in fort union lignite coals of North America

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

Laudal, Daniel A.; Benson, Steven A.; Addleman, Raymond Shane

Fort Union lignite coal samples were subjected to a series of aqueous leaching experiments to understand the extraction behavior of the rare earth elements (REE). This testing was aimed at understanding the modes of occurrence of the REE in the lignite coals, as well as to provide foundational data for development of rare earth extraction processes. In a first series of tests, a sequential leaching process was used to investigate modes of occurrence of the REE of select lignite coals. The tests involved sequential exposure to solvents consisting of water, ammonium acetate and dilute hydrochloric acid (HCl). The results indicatedmore » that water and ammonium acetate extracted very little of the REE, indicating the REE are not present as water soluble or ion-exchangeable forms. However, the data shows that a large percentage of the REE were extracted with the hydrochloric acid (80–95 wt%), suggesting presence in HCl-soluble mineral forms such as carbonates, and/or presence as organic complexes. A second series of tests was performed involving single-step leaching with dilute acids and various operating parameters, including acid type, acid concentration, acid/coal contact time and coal particle size. For select samples, additional tests were performed to understand the results of leaching, including float-sink density separations and humic acid extraction. The results have shown that the majority of REE in Fort Union lignites appear to be associated weakly with the organic matrix of the coals, most likely as coordination complexes of carboxylic acid groups. The light REE and heavy REE exhibit different behaviors, however. The extractable light REE appear to have association both in acid-soluble mineral forms and as organic complexes, whereas the extractable heavy REE appear to be almost solely associated with the organics. In conclusion, scandium behavior was notably different than yttrium and the lanthanides, and the data suggests the extractable content is primarily associated as acid-soluble mineral forms.« less

Geology of the Midnite uranium mine area, Washington: maps, description, and interpretation

USGS Publications Warehouse

Nash, J. Thomas

1977-01-01

Bedrock geology of about 12 km2 near the Midnite mine has been mapped at the surface, in mine exposures, and from drilling, at scales from 1:600 to 1:12,000 and is presented here at 1:12,000 to provide description of the setting of uranium deposits. Oldest rocks in the area are metapelitic and metacarbonate rocks of the Precambrian (Y) Togo Formation. The chief host for uranium deposits is graphitic and pyritic mica phyllite and muscovite schist. Ore also occurs in calc-silicate hornfels and marble at the western edge of a calcareous section about 1,150 m thick. Calcareous rocks of the Togo are probably older than the pelitic as they are interpreted to be near the axis of a broad anticline. The composition and structural position of the calcareous unit suggests correlation with less metamorphosed carbonate-bearing rocks of the Lower Wallace Formation, Belt Supergroup, about 200 km to the east. Basic sills intrusive into the Togo have been metamorphosed to amphibolite. Unmetamorphosed rocks in the mine area are Cretaceous(?) and Eocene igneous rocks. Porphyritic quartz monzonite of Cretaceous age, part of the Loon Lake batholith, is exposed over one third of the mine area. It underlies the roof pendant of Precambrian rocks in which the Midnite mine occurs at depths of generally less than 300 m. The pluton is a two-mica granite and exhibits pegmatitic and aplitic textural features indicative of water saturation and pressure quenching. Eocene intrusive and extrusive rocks in the area provide evidence that the Eocene surface was only a short distance above the present uranium deposits. Speculative hypotheses are presented for penesyngenetic, hydrothermal, and supergene modes of uranium emplacement. The Precambrian Stratigraphy, similar in age and pre-metamorphic lithology to that of rocks hosting large uranium deposits in Saskatchewan and Northern Territory, Australia, suggests the possibility of uranium accumulation along with diagenetic pyrite in carbonaceous muds in a marine shelf environment. This hypothesis is not favored by the author because there is no evidence for stratabound uranium such as high regional radioactivity in the Togo. A hydrothermal mode of uranium emplacement is supported by the close apparent ages of mineralization and plutonism, and by petrology of the pluton. I speculate that uranium may have become enriched in postmagmatic fluids at the top of the pluton, possibly by hydrothermal leaching of soluble uranium associated with magnetite, and diffused outward into metasedimentary wall rocks to create an aureole about 100 m thick containing about 100 ppm uranium. Chemistry of the hydrothermal process is not understood, but uranium does not appear to have been transported by an oxidizing fluid, and the fluid did not produce veining and alteration comparable to that of base-metal sulfide deposits. Uranium in the low-grade protore is believed to have been redistributed into permeable zones in the Tertiary to create ore grades. Geologic and isotopic ages of uranium mineralization, and the small volume of porphyritic quartz monzonite available for leaching, are not supportive of supergene emplacement of uranium.

APPARATUS FOR HIGH PURITY METAL RECOVERY

DOEpatents

Magel, T.T.

1959-02-10

An apparatus is described for preparing high purity metal such as uranium, plutonium and the like from an impure mass of the same metal. The apparatus is arranged so that the impure metal is heated and swept by a stream of hydrogen gas bearing a halogen such as iodine. The volatiie metal halide formed is carried on to a hot filament where the metal halide is decomposed and the molten high purity metal is collected in a rceeiver below

Fabrication of thorium bearing carbide fuels

DOEpatents

Gutierrez, R.L.; Herbst, R.J.; Johnson, K.W.R.

Thorium-uranium carbide and thorium-plutonium carbide fuel pellets have been fabricated by the carbothermic reduction process. Temperatures of 1750/sup 0/C and 2000/sup 0/C were used during the reduction cycle. Sintering temperatures of 1800/sup 0/C and 2000/sup 0/C were used to prepare fuel pellet densities of 87% and > 94% of theoretical, respectively. The process allows the fabrication of kilogram quantities of fuel with good reproductibility of chemical and phase composition.

Tanacetum vulgare as a bioindicator of trace-metal contamination: a study of a naturally colonized open-pit lignite mine.

PubMed

Jasion, Mateusz; Samecka-Cymerman, Aleksandra; Kolon, Krzysztof; Kempers, Alexander J

2013-10-01

We investigated the possibility of use of Tanacetum vulgare (tansy) as an ecological indicator of metal concentration in a naturally colonized open-pit lignite mine in Bełchatów (Poland). Tanacetum vulgare is the only species growing abundantly and spontaneously in the lignite mine waste dumps. Metal concentrations in roots, stems, leaves, flowers, and soil were measured in dump sites differing in type and time of reclamation and therefore differing in pollution levels. Tanacetum vulgare appeared to be an accumulator of chromium and iron in roots, whereas highest concentrations of manganese and zinc were found in leaves. A high bioaccumulation factor for cadmium (Cd) was observed in dumps and control sites, indicating that even small amounts of Cd in the environment may result in significant uptake by the plant. The lowest concentrations of metals were found in plants from sites situated on dumps reclaimed with argillaceous limestone.

Production of Low Enriched Uranium Nitride Kernels for TRISO Particle Irradiation Testing

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

McMurray, J. W.; Silva, C. M.; Helmreich, G. W.

2016-06-01

A large batch of UN microspheres to be used as kernels for TRISO particle fuel was produced using carbothermic reduction and nitriding of a sol-gel feedstock bearing tailored amounts of low-enriched uranium (LEU) oxide and carbon. The process parameters, established in a previous study, produced phasepure NaCl structure UN with dissolved C on the N sublattice. The composition, calculated by refinement of the lattice parameter from X-ray diffraction, was determined to be UC 0.27N 0.73. The final accepted product weighed 197.4 g. The microspheres had an average diameter of 797±1.35 μm and a composite mean theoretical density of 89.9±0.5% formore » a solid solution of UC and UN with the same atomic ratio; both values are reported with their corresponding calculated standard error.« less

Elucidating bonding preferences in tetrakis(imido)uranate(VI) dianions

NASA Astrophysics Data System (ADS)

Anderson, Nickolas H.; Xie, Jing; Ray, Debmalya; Zeller, Matthias; Gagliardi, Laura; Bart, Suzanne C.

2017-09-01

Actinyl species, [AnO2]2+, are well-known derivatives of the f-block because of their natural occurrence and essential roles in the nuclear fuel cycle. Along with their nitrogen analogues, [An(NR)2]2+, actinyls are characterized by their two strong trans-An-element multiple bonds, a consequence of the inverse trans influence. We report that these robust bonds can be weakened significantly by increasing the number of multiple bonds to uranium, as demonstrated by a family of uranium(VI) dianions bearing four U-N multiple bonds, [M]2[U(NR)4] (M = Li, Na, K, Rb, Cs). Their geometry is dictated by cation coordination and sterics rather than by electronic factors. Multiple bond weakening by the addition of strong π donors has the potential for applications in the processing of high-valent actinyls, commonly found in environmental pollutants and spent nuclear fuels.

Nuclear fuels for very high temperature applications

NASA Astrophysics Data System (ADS)

Lundberg, L. B.; Hobbins, R. R.

The success of the development of nuclear thermal propulsion devices and thermionic space nuclear power generation systems depends on the successful utilization of nuclear fuel materials at temperatures in the range 2000 to 3500 K. Problems associated with the utilization of uranium bearing fuel materials at these very high temperatures while maintaining them in the solid state for the required operating times are addressed. The critical issues addressed include evaporation, melting, reactor neutron spectrum, high temperature chemical stability, fabrication, fission induced swelling, fission product release, high temperature creep, thermal shock resistance, and fuel density, both mass and fissile atom. Candidate fuel materials for this temperature range are based on UO2 or uranium carbides. Evaporation suppression, such as a sealed cladding, is required for either fuel base. Nuclear performance data needed for design are sparse for all candidate fuel forms in this temperature range, especially at the higher temperatures.

Influence of Acid Mine Drainage (AMD) on recent phyto- and zooplankton in "the Anthropogenic Lake District" in south-west Poland

NASA Astrophysics Data System (ADS)

Sienkiewicz, Elwira; Gasiorowski, Michal

2015-04-01

In south-west Poland (central Europe) many the post-mining lakes formed so-called "the Anthropogenic Lake District". Areas, where water comes in contact with lignite beds characterized by high concentration of sulfide minerals are called Acid Mine Drainage (AMD). Pyrite oxidation and other sulfide compounds caused release sulfuric acids and heavy metal ions. These processes caused decline of water pH, sometimes to extremely low pH < 2.8. Presently, pit lakes located in south-west Poland have water pH ranged between 2.7 and 8.9. Differences of water reaction in the mine lakes depend on many factors, such as bedrock buffer capacity, geological structure of carboniferous area, exploitation technique of lignite, methods of filling and water supply of reservoirs and their age. During the evolution of lakes' ecosystems, sulfate-iron-calcium type of waters occurring in acid lakes will transform in alkaline hydrogen-carbonate-calcium type of waters. Due to the different time of the completion of lignite exploitation, lakes' age varied between forty and over one hundred years. Studies showed that younger lakes are more acidic in compare to older. To estimate impact of AMD we analyzed recent diversity of diatoms and Cladocera remains and water chemistry from extremely acidic, relatively young lakes and from alkaline, older water bodies. As we expected, flora and fauna from acidic lakes have shown very low diversity and species richness. Among diatoms, Eunotia exigua (Bréb. ex Kütz.) Rabenhorst and/or E. paludosa Grunow were dominated taxa, while fauna Cladocera did not occurred in lakes with water pH < 3. On this area, exploitation of lignite continued up to 1973. Older lakes were formed in the region where the mine started work in 1880 and lignite mining stopped in 1926. Measurements of pH value in situ point to neutral or alkaline water, but because of the possibility of hysteresis phenomenon, the studies of phyto- and zooplankton have shown if there has already been a widespread neutralization of lake ecosystems, what encompassing both recovery of water chemistry and rebuilding of biota communities. Studies have confirmed, that phyto- and zooplankton living nowadays in lakes located on this area, where exploitation of lignite ended at the beginning of 20th century, indicate completely recovery from acidification caused by coal mine activities. Presently, the lakes were dominated by planktonic diatoms and Cladocera taxa, such as Discostella pseudostelligera (Hust.) Houk & Klee and Bosmina longirostris, respectively.

Hydrological, geological, and biological site characterization of breccia pipe uranium deposits in Northern Arizona

USGS Publications Warehouse

Alpine, Andrea E.

2010-01-01

On July 21, 2009, U.S. Secretary of the Interior Ken Salazar proposed a two-year withdrawal of about 1 million acres of Federal land near the Grand Canyon from future mineral entry. These lands are contained in three parcels: two parcels on U.S. Bureau of Land Management land to the north of the Grand Canyon (North and East Segregation Areas) and one on the Kaibab National Forest south of the Grand Canyon (South Segregation Area). The purpose of the two-year withdrawal is to examine the potential effects of restricting these areas from new mine development for the next 20 years. This proposed withdrawal initiated a period of study during which the effects of the withdrawal must be evaluated. At the direction of the Secretary, the U.S. Geological Survey began a series of short-term studies designed to develop additional information about the possible effects of uranium mining on the natural resources of the region. Dissolved uranium and other major, minor, and trace elements occur naturally in groundwater as the result of precipitation infiltrating from the surface to water-bearing zones and, presumably, to underlying regional aquifers. Discharges from these aquifers occur as seeps and springs throughout the region and provide valuable habitat and water sources for plants and animals. Uranium mining within the watershed may increase the amount of radioactive materials and heavy metals in the surface water and groundwater flowing into Grand Canyon National Park and the Colorado River, and deep mining activities may increase mobilization of uranium through the rock strata into the aquifers. In addition, waste rock and ore from mined areas may be transported away from the mines by wind and runoff.

Microbial communities associated with uranium in-situ recovery mining process are related to acid mine drainage assemblages.

PubMed

Coral, Thomas; Descostes, Michaël; De Boissezon, Hélène; Bernier-Latmani, Rizlan; de Alencastro, Luiz Felippe; Rossi, Pierre

2018-07-01

A large fraction (47%) of the world's uranium is mined by a technique called "In Situ Recovery" (ISR). This mining technique involves the injection of a leaching fluid (acidic or alkaline) into a uranium-bearing aquifer and the pumping of the resulting solution through cation exchange columns for the recovery of dissolved uranium. The present study reports the in-depth alterations brought to autochthonous microbial communities during acidic ISR activities. Water samples were collected from a uranium roll-front deposit that is part of an ISR mine in operation (Tortkuduk, Kazakhstan). Water samples were obtained at a depth of ca 500 m below ground level from several zones of the Uyuk aquifer following the natural redox zonation inherited from the roll front deposit, including the native mineralized orebody and both upstream and downstream adjacent locations. Samples were collected equally from both the entrance and the exit of the uranium concentration plant. Next-generation sequencing data showed that the redox gradient shaped the community structures, within the anaerobic, reduced, and oligotrophic habitats of the native aquifer zones. Acid injection induced drastic changes in the structures of these communities, with a large decrease in both cell numbers and diversity. Communities present in the acidified (pH values < 2) mining areas exhibited similarities to those present in acid mine drainage, with the dominance of Sulfobacillus sp., Leptospirillum sp. and Acidithiobacillus sp., as well as the archaean Ferroplasma sp. Communities located up- and downstream of the mineralized zone under ISR and affected by acidic fluids were blended with additional facultative anaerobic and acidophilic microorganisms. These mixed biomes may be suitable communities for the natural attenuation of ISR mining-affected subsurface through the reduction of metals and sulfate. Assessing the effect of acidification on the microbial community is critical to evaluating the potential for natural attenuation or active bioremediation strategies. Copyright © 2018 Elsevier B.V. All rights reserved.

The geochemistry of water near a surficial organic-rich uranium deposit, northeastern Washington State, U.S.A.

USGS Publications Warehouse

Zielinski, R.A.; Otton, J.K.; Wanty, R.B.; Pierson, C.T.

1987-01-01

The chemistry of three stream, three spring and six near-surface waters in the vicinity of a Holocene organic-rich uranium deposit is described, with particular emphasis on the chemistry of U. Results characterize the solution behavior of uranium as U-bearing water interacts with relatively undecomposed, surficial organic matter. Of the measured major and trace chemical species, only U is consistently highly enriched (17-318 ppb) relative to reported values for regional waters, or to literature values for waters in largely granitic terrains. R-mode factor analysis of the chemical data suggests that most U is present in a soluble form, but that some U is also associated with fine suspended particulates of clay, organic matter, or hydrous oxides. Calculations that apply thermodynamic data to predict U speciation in solution indicate the relative importance of uranyl carbonate and uranyl phosphate complexes. Analysis of more finely filtered samples (0.05 ??m vs. 0.45 ??m), and direct radiographic observations using fission-track detectors suspended in the waters indicate the presence of some uraniferous particulate matter. Application of existing thermodynamic data for uranous- and uranyl-bearing minerals indicates that all waters are undersaturated with U minerals as long as ambient Eh ??? +0.1 v. If coexisting surface and near-surface waters are sufficiently oxidizing, initial fixation of U in the deposit should be by a mechanism of adsorption. Alternatively, more reducing conditions may prevail in deeper pore waters of the organic-rich host sediments, perhaps leading to direct precipitation or diagenetic formation of U4+ minerals. A 234U 238U alpha activity ratio of 1.08 ?? 0.02 in a spring issuing from a hillslope above the deposit suggests a relatively soluble source of U. In contrast, higher activity ratios of 234U 238U (??? 1.3) in waters in contact with the uraniferous valley-fill sediments suggest differences in the nature of interaction between groundwater and the local, U-rich source rocks. ?? 1987.

Approaches to Post-Mining Land Reclamation in Polish Open-Cast Lignite Mining

NASA Astrophysics Data System (ADS)

Kasztelewicz, Zbigniew

2014-06-01

The paper presents the situation regarding the reclamation of post-mining land in the case of particular lignite mines in Poland until 2012 against the background of the whole opencast mining. It discusses the process of land purchase for mining operations and its sales after reclamation. It presents the achievements of mines in the reclamation and regeneration of post-mining land as a result of which-after development processes carried out according to European standards-it now serves the inhabitants as a recreational area that increases the attractiveness of the regions.

Laboratory analysis and airborne detection of materials stimulated to luminesce by the sun

USGS Publications Warehouse

Hemphill, W.R.; Theisen, A.F.; Tyson, R.M.

1984-01-01

The Fraunhofer line discriminator (FLD) is an airborne electro-optical device used to image materials which have been stimulated to luminesce by the Sun. Such materials include uranium-bearing sandstone, sedimentary phosphate rock, marine oil seeps, and stressed vegetation. Prior to conducting an airborne survey, a fluorescence spectrometer may be used in the laboratory to determine the spectral region where samples of the target material exhibit maximum luminescence, and to select the optimum Fraunhofer line. ?? 1984.

Method for preparing hydride configurations and reactive metal surfaces

DOEpatents

Silver, G.L.

1984-05-18

A method for preparing reactive metal surfaces, particularly uranium surfaces is disclosed, whereby the metal is immediately reactive to hydrogen gas at room temperature and low pressure. The metal surfaces are first pretreated by exposure to an acid which forms an adherent hydride-bearing composition on the metal surface. Subsequent heating of the pretreated metal at a temperature sufficient to decompose the hydride coating in vacuum or inert gas renders the metal surface instantaneously reactive to hydrogen gas at room temperature and low pressure.

Studying Legacy Uranium Contamination On Navajo, Laguna, and Isleta Lands In Collaboration With Native American Undergraduate Researchers

NASA Astrophysics Data System (ADS)

Cadol, D. D.; Frey, B.; Chee, C.

2017-12-01

Personally relevant research experiences at key points in a student's education are potentially powerful influences on their long-term career path. With this in mind, New Mexico EPSCoR created the STEM Advancement Program (STEMAP) to provide a summer research experience for students from the non-graduate-degree granting institutions in New Mexico. Recruitment focused on underrepresented minorities, primarily Native American and Hispanic students, who applied to work with one of six research components. Our research component focused on understanding the fate and transport of environmental uranium in the Four Corners region. The geosciences are especially amenable to providing meaningful research experiences, particularly for groups that have a strong cultural connection with the land. Uranium mining activities were extensive on several reservations in the 1950s to 1980s, and many of the sites have not been remediated. The impact of mining likely contributed to the high interest among Native American (especially Navajo) STEMAP applicants in this research topic. In four years of summer research we mentored four Native American students (two male and two female) and one white non-Hispanic female. Following their work in our research group, one student extended her research, three graduated, and one transferred to a research institution. This success likely reflects a combination of recruitment efforts, which built on community connections, as well as efforts to provide personal mentoring and to create an inclusive environment. The work of these students has advanced our understanding of fluvial transport of uranium from inactive mining districts, an important pathway given the role of these streams in providing water for agriculture and aggregate for construction. Findings demonstrate an affinity of uranium to sorb to fine-grained sediment, meaning standing water in stock ponds is of particular concern. The students also studied uranium-bearing dust generated from legacy sites, documenting dissolution of uranium in two contrasting simulated lung fluids. Student presentations in the affected communities closed the communication loop, presenting findings in an accessible format. Ideally these presentations also planted seeds of interest in the geosciences for younger community members.

Dibutyl Phosphoric Acid Solubility in High-Acid, Uranium-Bearing Solutions at SRS

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

Pierce, R.A.

1998-10-02

The Savannah River Site has enriched uranium (EU) solution which has been stored for almost 10 years since being purified in the second uranium cycle of the H area solvent extraction process. The concentrations in solution are approximately 6 g/L U and about 0.1 M nitric acid. Residual tributylphosphate in the solutions has slowly hydrolyzed to form dibutyl phosphoric acid (HDBP) at concentrations averaging 50 mg/L. Uranium is known to form compounds with the dibutylphosphate ion (DBP) which have limited solubility. The potential to form uranium-DBP solids raises a nuclear criticality safety issue. Prior SRTC tests (WSRC-TR-98-00188) showed that U-DBPmore » solids precipitate at concentrations potentially attainable during the storage of enriched uranium solutions. Furthermore, evaporation of the existing EUS solution without additional acidification could result in the precipitation of U-DBP solids if the DBP concentration in the resulting solution exceeds 110 mg/L at ambient temperature. The same potential exists for evaporation of unwashed 1CU solutions. As a follow-up to the earlier studies, SRTC studied the solubility limits for solutions containing acid concentrations above 0.5M HNO3. The data obtained in these tests reveals a shift to higher levels of DBP solubility above 0.5M HNO3 for both 6 g/L and 12 g/L uranium solutions. Analysis of U-DBP solids from the tests identified a mixture of different molecular structures for the solids created. The analysis distinguished UO2(DBP)2 as the dominant compound present at low acid concentrations. As the acid concentration increases, the crystalline UO2(DBP)2 shows molecular substitutions and an increase in amorphous content. Further analysis by methods not available at SRS will be needed to better identify the specific compounds present. This data indicates that acidification prior to evaporation can be used to increase the margin of safety for the storage of the EUS solutions. Subsequent experimentation evaluated options for absorbing HDBP from solution using either activated carbon or anion exchange resin. The activated carbon outperformed the anion exchange resin. Activated carbon absorbs DBP rapidly and has demonstrated the capability of absorbing 15 mg of DBP per gram of activated carbon. Analytical results also show that activated carbon absorbs uranium up to 17 mg per gram of carbon. It is speculated that the uranium absorbed is part of a soluble U-DBP complex that has been absorbed. Additional testing must still be performed to 1) establish absorption limits for uranium for anion exchange resin, 2) evaluate desorption characteristics of uranium and DBP, and 3) study the possibility of re-using the absorbent.« less

Nanoscale Zirconium-(oxyhydr)oxide in Contaminated Sediments From Hanford, WA - A New Host for Uranium

NASA Astrophysics Data System (ADS)

Stubbs, J. E.; Elbert, D. C.; Veblen, L. A.; Zachara, J. M.; Davis, J. A.; Veblen, D. R.

2008-12-01

Zirconium-, uranium-, and copper-bearing wastes have leached from former disposal ponds into vadose zone sediments in the 300 Area at the Department of Energy's Hanford Site. Zirconium is enriched in the shallow portion of the vadose zone, and we have discovered an amorphous Zr-(oxyhydr)oxide that contains 16% of the total uranium budget (84.24 ppm) in one of the shallow samples. We have characterized the oxide using electron microprobe analysis (EMPA), a focused ion beam (FIB) instrument, and transmission electron microscopy (TEM). It occurs in fine-grained coatings found on lithic and mineral fragments in these sediments. The oxide is intimately intergrown with the phyllosilicates and other minerals of the coatings, and in places can be seen coating individual, nano-sized phyllosilicate mineral grains. Electron energy-loss spectroscopy (EELS) shows that the Zr-(oxyhydr)oxide has a P:Zr atomic ratio around 0.2, suggesting it is either intergrown with minor amounts of a Zr-phosphate or has adsorbed a significant amount of phosphate. This material has adsorbed or incorporated a substantial amount of uranium. Thus, understanding its nature is critical to predicting the long-term fate of U in the Hanford vadose zone. While the low-temperature uptake of U by Zr-(oxhydr)oxides and phosphates has been studied for several decades in laboratory settings, to our knowledge ours is the first report of such uptake in the field.

The geohydrologic system and probable effects of mining in the Sand Creek-Hanks lignite area, western Williams County, North Dakota

USGS Publications Warehouse

Armstrong, C.A.

1985-01-01

The investigation was undertaken to define the geohydrology of the Sand Creek-Hanks area and to project probable hydrologic effects of lignite mining on the area. Aquifers occur in sandstone beds in the Fox Hills Sandstone and the Hell Creek Formation of Cretaceous age and in sandstone lenses and lignite beds in the Tongue River and Sentinel Butte Members of the Fort Union Formation of Tertiary age.The top of the Fox Hills aquifer ranges from about 1,200 to 2,000 feet below land surface. Yields of wells completed in the aquifer could be as much as 60 gallons per minute. Water in the Fox Hills aquifer is a sodium bicarbonate type and generallyDepths to the top of the Hell Creek aquifer range from about 900 to 1,600 feet. Well yields range from less than 10 to 40 gallons per minute. Water in the aquifer is a sodium bicarbonate type and generally contains between 1,000 and 2,200 milligrams per liter dissolved solids. Depths to aquifers in the Tongue River and Sentinel Butte Members of Fort Union Formation range from near land surface to about 1,000 feet below land surface. Wells completed in the aquifers may yield as much as 40 gallons per minute of sodium bicarbonate or a sodium sulfate type water that contains about 800 to 4,100 milligrams per liter dissolved solids.Glacial drift covers most of the study area. The drift thickness ranges from a veneer to about 380 feet. Well yields range from a few gallons per minute to 900 gallons per minute. Dissolved-solids concentrations in water from the glacial drift generally range from 477 to 2,050 milligrams per liter. Mining of lignite will destroy all aquifers in and above the mined lignite and will expose overburden to oxidation. Leaching will cause an increase in dissolved solids in ground water immediately beneath the mines and possibly will cause some increase in the dissolved solids in low flows in area streams.

Design assessment of a 150 kWt CFBC Test Unit

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

Batu, A.; Selcuk, N.; Kulah, G.

2010-04-15

For clean and efficient energy generation from coal, the most suitable technology known to date is 'Fluidized Bed Combustion' technology. Applications of circulating fluidized bed (CFB) combustion technology have been steadily increasing in both capacity and number over the past decade. Designs of these units have been based on the combustion tests carried out in pilot scale facilities to determine the combustion and desulfurization characteristics of coal and limestone reserves in CFB conditions. Similarly, utilization of Turkish lignites in CFB boilers necessitates adaptation of CFB combustion technology to these resources. However, the design of these test units are not basedmore » on firing coals with high ash, volatile matter and sulfur contents like Turkish lignites. For this purpose, a 150 kWt CFB combustor test unit is designed and constructed in Chemical Engineering Department of Middle East Technical University, based on the extensive experience acquired at the existing 0.3 MWt Bubbling Atmospheric Fluidized Bed Combustor (AFBC) Test Rig. Following the commissioning tests, a combustion test is carried out for investigation of combustion characteristics of Can lignite in CFB conditions and for assessment of the design of test unit. Comparison of the design outputs with experimental results reveals that most of the predictions and assumptions have acceptable agreement with the operating conditions. In conclusion, the performance of 150 kWt CFBC Test Unit is found to be satisfactory to be utilized for the long term research studies on combustion and desulfurization characteristics of indigenous lignite reserves in circulating fluidized bed combustors. (author)« less

Research on a new type of additive for CWS from low temperature pyrolysis tar

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

Wu Guoguang; Wang Zuna

1997-12-31

In this paper, coal tar from flash pyrolysis of Ping Zhuang lignite with solid heat carrier was used as raw material, which was directly synthesized a new type of additive for coal water slurry (CWS) in the laboratory. The wetting heat between the lignite and distilled water and solution of additive has been determined. It is evident that the wetting heat between the lignite and distilled water is very high, up to 44.56 J/g, which is harmful to preparing CWS. The wetting heat between the lignite and a solution of additive is reduced, which is related to its characteristics suchmore » as surface properties, oxygen functional groups and structure. The effect of coal properties on preparing CWS has also been analyzed systematically. It is suggested that the concentration of CWS is regularly changed with oxygen content of coal based on moisture and ash content. It is emphasized that when the influence of macerals on slurriability of coal is observed, inherent properties of each maceral such as pore structure, porosity, oxygen functional groups, grindability must be tightly combined to evaluate comprehensively. The structural characteristics of the additive matches well the molecular structure and surface properties of the coal. It is seen by synthetic experiments that suitable a degree of sulphonating and condensation are beneficial to preparing CWS. The rheology and stability of CWS have also been investigated. The result indicates that the stability of CWS using the new type of additive is improved, and the production cost of the additive synthesized from low temperature pyrolysis coal tar can be reduced.« less

Radiostratigraphic study of the deposits of the Maikop Group, Western Azerbaijan

NASA Astrophysics Data System (ADS)

Efendieva, M.; Babaev, R.; Johnson, C.; Feyzullayev, A.; Aliev, Ch.

2012-11-01

This work presents the results of biostratigraphic study of natural outcrops of the Maikop Group, which were first carried together with detailed radiometric studies in the Ganja oil and gas-bearing region, Western Azerbaijan. The paleontological research method included determination of the genus or species (depending on the preservation) of microfaunistic remains (foraminifera, ostracods, fish remains). The radiometric research method included measurements of the integral radioactivity in the field, the sampling, as well as laboratory radionuclide (spectral) analysis. As a result of our research, the stratigraphic control of variation in the radioactivity of rocks of the Maikop Group of the Ganja oil and gas-bearing region has been established. The radioactivity of Oligocene rocks is predominantly determined by potassium content. The radioactivity of the Miocene part of the section of the Maikop Group is determined by uranium-potassium contents. Within the Ganja oil and gas-bearing region, deposits of the Kotsakhurian regional stage, which are usually referred to "barren" formations or anoxic "fish facies", contain a significant number of species of benthic foraminiferal fauna.

Isotherm and thermodynamic studies of Zn (II) adsorption on lignite and coconut shell-based activated carbon fiber.

PubMed

Shrestha, Sohan; Son, Guntae; Lee, Seung Hwan; Lee, Tae Gwan

2013-08-01

The Zn (II) adsorption capacity of lignite and coconut shell-based activated carbon fiber (ACF) was evaluated as a function of initial Zn (II) concentration, temperature and contact time in batch adsorption process in this study. Adsorption uptake increased with initial Zn (II) concentration and temperature. Optimal contact time for the adsorption of Zn (II) ions onto lignite and coconut shell-based ACF was found to be 50 min. Removal percentage decreased from 88.0% to 78.54% with the increment in initial Zn (II) concentration from 5 to 50 mg L(-1). Equilibrium data fit well with Langmuir-I isotherm indicating homogeneous monolayer coverage of Zn (II) ions on the adsorbent surface. Maximum monolayer adsorption capacity of Zn (II) ions on ACF was found to be 9.43 mg g(-1). Surface morphology and functionality of ACF prior to and after adsorption were characterized by electron microscopy and infrared spectroscopy. Various thermodynamic parameters such as standard Gibbs free energy (ΔG°), standard enthalpy (ΔH°), and standard entropy (ΔS°) were evaluated. Copyright © 2013 Elsevier Ltd. All rights reserved.

Cleaner co-combustion of lignite-biomass-waste blends by utilising inhibiting compounds of toxic emissions.

PubMed

Skodras, G; Palladas, A; Kaldis, S P; Sakellaropoulos, G P

2007-04-01

In this paper, the co-combustion behaviour of coal with wastes and biomass and the related toxic gaseous emissions were investigated. The objective of this work is to add on towards a cleaner co-combustion of lignite-waste-biomass blends by utilizing compounds that could inhibit the formation of toxic pollutants. A series of co-combustion tests was performed in a pilot scale incinerator, and the emissions of polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) were measured. The co-combustion behaviour of lignite with olive kernels, MDF and sawdust was studied and the ability of additives such as urea, almond shells and municipal sewage sludge to reduce the PCDD/F emissions was examined. All blends were proven good fuels and reproducible combustion conditions were achieved. The addition of inhibitors prior to combustion showed in some cases, relatively high PCDD/F emissions reduction. Among the inhibitors tested, urea seems to achieve a reduction of PCDD/F emissions for all fuel blends, while an unstable behaviour was observed for the others.

The influence of organic substances type on the properties of mineral-organic fertilizers

NASA Astrophysics Data System (ADS)

Huculak-Mä Czka, Marta; Hoffmann, Krystyna; Hoffmann, Józef

2010-05-01

In presented research the lignite coal, peat, poultry droppings and their composts were suggested as a components of mineral-organic fertilizers. Fertility of soil is conditioned by an ability to supply plants with water and nutrients essential to their growth and development. The soil is described as tri-phase system consisting of solid, liquid and gas phase. In solid phase the soil minerals and organic matter can be distinguished. The content of micro-organisms contained in the soil i.e. microfauna and microflora is indispensable for high soil fertility. Nutrients should occur in the forms available for plants in order to obtain high yields of the high quality crops. Organic fertilizing has versatile activity. Increasing contents of humus, providing mineral nutrients included in organic substance and the improvement in physical properties of the soil belong to its main purposes. Due to applying organic fertilizers heavy soils is getting loosen and in consequence become more airy what probably influences stimulation of soil micro-organisms activity. An aqueous as well as sorption capacity of light soils is also increasing, buffer range and the stabilization of the proper level of pH value of the soil, plants are provided with basic macro and micronutrients. Conventional organic fertilizers applied in an arable farms are manure, dung, green manures and composts of different kind. Within compost group the following types can be distinguished: compost from farming, urban wastes, shredded straw, poultry droppings, industrial wastes, bark of coniferous tree etc. Properly developed fertilizer formulas should contain in their composition both mineral as well as organic elements. Such fertilizer should fit its composition to the soil and plant requirements. It should contain organic substance being characterized by a high aqueous and cations sorption capacity, substance undergoing the fast mineralization with the large calcium content. Inorganic substances e.g. bentonites which are used for suspension fertilizers manufacturing meet these requirements as well. In the presented studies lignite coal was applied as a component of mineral-organic preparations. The advantages of lignite coal are positive influence on the soil heat balance and reduction of the temperature fluctuations influence as well as humic acids contents that are extracted during its decomposition improving the soil structure and enrichment with humus substances. The lignite coal used in examinations contained 50 - 60 wt. % of Corg, about 45 cmol/kg Ca, 18.5 cmol/kg Mg and P, K, N in the ppm amount. Unfortunately the fertilizer components included in the lignite coal are rather unavailable for plants. It seems, that progress of lignite coal mineralization and humification can be expressed in the increasing content of humus substances. Humus acids are of great importance for plants on account of their solubility. During examination on the selection of fertilizer components a Corg content was analyzed as a parameter determining the quality of mineral-organic preparations. As the analytical technique for Corg determination particularly a Tiurin method was applied. Apart from lignite coal and peat as the source of organic substance the poultry droppings and compost on their basis were analyzed. Poultry droppings depending on bird species as well as feeding and breeding method are characterized by variable composition. A high pH values and a large content of nitrogen are their distinctive features, sometimes too high on account of plant nutritional requirements, and toxic as well as limiting cropping. Taking environmental protection requirements into consideration as well as on account of proper plants nutrition an appropriate preparation of mineral-organic fertilizer is recommended what can be obtained by applying lignite coal and poultry droppings as components of fertilizer using appropriate proportion. Adapting composted poultry droppings is more beneficial, but requires extra financial outlays. Results obtained from examinations of organic substance and the investigations on the influence of components on plants germination allow for developing valid formulas for mineral-organic fertilizers.

A preliminary evaluation of the nonfuel mineral potential of Somalia

USGS Publications Warehouse

Greenwood, W.R.

1982-01-01

Additional exploration in Somalia is warranted for a wide variety of metallic and nonmetallic deposits. In Precambrian rocks, deposit types favorable for exploration include: a banded iron formation; platinum-bearing mafic-ultramafic complexes; tin-bearing quartz veins; phosphorite; stratabound base-metal deposits; uranium associated with Precambrian(?) syenite; apatite, molybdenum, and alumina in alkalic rocks; Jurassic and Cretaceous black shales; possible bedded-barite and massive base- and precious-metal sulfide deposits; vein barite in Tertiary rocks in fault zones; sepiolite and bentonite for drilling muds and other industrial uses; celestite; possible Tertiary zeolite; and uranium deposits. Several of these deposit types could be Jointly developed and integrated into domestic industries; for example, phosphate and gypsum, or bentonite for pelletized iron from the banded iron deposits. Other deposits such as barite and sepiolite are of value because of their proximity to major drilling operations in the Arabian Gulf. Still other deposits, such as alumina and banded iron, might be marketable because of proximity to aluminum and iron-refining industries now being constructed in Saudi Arabia. Some deposits, such as celestite, can be developed with little capital investment; others, such as the iron deposits, would require large capital commitments. Exploration and evaluation for many of these deposits can be accomplished by Somali geologists with a few advisors. Most of the deposits require feasibility studies conducted by teams of economic geologists, extractive metallurgists, and economists. Some marginal deposits could be exploited if cooperative development schemes could be negotiated with governments in nearby countries.

Biodegradation and bioconversion of coals by fungi: Technical report No. 6 for the period December 1, 1986-February 28, 1987. [Candida sp. , Cunninghamella sp. , Acremonium sp. , and Trametes versicolor

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

Ward, B.

We continued our tests for biosolubilization activity on lignite, subbituminous, and bituminous coals, using both surface solubilization and agar diffusion assays for selected lignite-solubilizing strains challenged with untreated and treated coals shown in earlier tests to be resistant to biosolubilization. These latter were subjected to treatments with heat or pressurized oxygen atmosphere, or to combinations of the same. We have observed biosolubilization of some weathered high-rank coals by some of the fungal isolates tested. 1 tab.

Drilling fluid

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

Russell, J.A.; Patel, B.B.

1987-11-03

A drilling fluid additive mixture is described consisting essentially of a sulfoalkylated tannin in admixture with a non-sulfoalkylated alkali-solubilized lignite wherein the weight ratio of the sulfoalkylated tannin to the non-sulfoalkylated lignite is in the range from about 2:1 to about 1:1. The sulfoalkylated tannin has been sulfoalkylated with at least one -(C(R-)/sub 2/-SO/sub 3/M side chain, wherein each R is selected from the group consisting of hydrogen and alkyl radicals containing from 1 to about 5 carbon atoms, and M is selected from the group consisting of ammonium and the alkali metals.

Injection of Emulsified Vegetable Oil for Long-Term Bioreduction of Uranium

NASA Astrophysics Data System (ADS)

Brooks, S. C.; Watson, D. B.; Schadt, C. W.; Jardine, P. M.; Gihring, T. M.; Zhang, G.; Mehlhorn, T.; Lowe, K.; Phillips, J.; Earles, J.; Wu, W.; Criddle, C. S.; Kemner, K. M.; Boyanov, M.

2011-12-01

In situ bioremediation of a uranium and nitrate-contaminated aquifer with the slow-release electron donor, emulsified vegetable oil (EVO), was tested at the US DOE Subsurface Biogeochemical Research Program (SBR) Integrated Field Research Challenge (IFRC) site, in Oak Ridge, TN. The EVO injection took place in Area 2 of the IFRC located about 300 m downgradient of the former S-3 disposal ponds. Liquid wastes, disposed in the ponds from 1951 to 1983, were primarily composed of nitric acid, plating wastes containing various metals (Cr, Ni) radionuclides (U, Tc), inorganics (nitrate, sulfate) and organic contaminants (tetrachloroethylene, acetone). Prior pond closure in 1987, large volumes of waste fluids migrated into the subsurface, down Bear Creek Valley and into Bear Creek. Contaminants detected at Area 2 were transported through a high permeability gravelly fill that is considered a preferred transport pathway for U to Bear Creek. Groundwater in the gravelly fill is contaminated with U (1-3 mg/L), sulfate (95-130 mg/L), and nitrate (20-40 mg/L) and 500 mg/kg or higher U has been detected on the solid phase of the fill material. The objective of this study is to investigate the feasibility and long-term sustainability of U(VI) reduction and immobilization, and nitrate degradation in the high permeability, high flow gravel fill using EVO as the electron donor. A one-time EVO injection was conducted over a 2 hour period in the highly permeable gravel (hydraulic conductivity 0.08 cm/sec) in the well instrumented IFRC Area 2 field plot. Extensive monitoring of geochemical parameters, dissolved gases and microbial populations were conducted during the test. A bromide tracer test was conducted prior to the injection of the EVO to assess transport pathways and rates. Geochemical analysis of site groundwater demonstrated the sequential bioreduction of oxygen, nitrate, Mn(IV), Fe(III) and sulfate. Transient accumulation of acetate was observed as an intermediate in the oil degradation. Reduction and removal of U and nitrate from groundwater was observed in all wells in hydraulic connection to the injection wells after 2-4 weeks. U concentrations in groundwater were reduced to below 30 ppb (US EPA drinking water standard) at some well locations and nitrate was reduced to below detectable levels. Rebound of U in groundwater was observed together with the rebound of sulfate concentrations as the EVO was consumed. The flux of U and nitrate contamination from groundwater to the surface water receptor (Bear Creek) was significantly reduced by the EVO injection over a one year period. Uranium (VI) reduction to U(IV) in the field tests was confirmed by X-ray absorption near-edge spectroscopy (XANES) analysis. The reduced U(IV) was determined by X-ray absorption fine structure (XAFS) to be in an Fe-U complex, not uraninite. The activities of major Fe(III)- and sulfate-reducing bacteria with U(VI)-reducing capability as well as methanogens was stimulated after injection of the oil.

The effect of Si and Al concentrations on the removal of U(VI) in the alkaline conditions created by NH3 gas

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

Katsenovich, Yelena P.; Cardona, Claudia; Lapierre, Robert

2016-10-01

Remediation of uranium in the deep unsaturated zone is a challenging task, especially in the presence of oxygenated, high-carbonate alkalinity soil and pore water composition typical for arid and semi-arid environments of the western regions of the U.S. This study evaluates the effect of various pore water constituencies on changes of uranium concentrations in alkaline conditions, created in the presence of reactive gases such as NH3 to effectively mitigate uranium contamination in the vadose zone sediments. This contaminant is a potential source for groundwater pollution through slow infiltration of soluble and highly mobile uranium species towards the water table. Themore » objective of this research was to evaluate uranium sequestration efficiencies in the alkaline synthetic pore water solutions prepared in a broad range of Si, Al, and bicarbonate concentrations typically present in field systems of the western U.S. regions and identify solid uranium-bearing phases that result from ammonia gas treatment. In previous studies (Szecsody et al. 2012; Zhong et al. 2015), although uranium mobility was greatly decreased, solid phases could not be identified at the low uranium concentrations in field-contaminated sediments. The chemical composition of the synthetic pore water used in the experiments varied for silica (5–250 mM), Al3+ (2.8 or 5 mM), HCO3- (0–100 mM) and U(VI) (0.0021–0.0084 mM) in the solution mixture. Experiment results suggested that solutions with Si concentrations higher than 50 mM exhibited greater removal efficiencies of U(VI). Solutions with higher concentrations of bicarbonate also exhibited greater removal efficiencies for Si, Al, and U(VI). Overall, the silica polymerization reaction leading to the formation of Si gel correlated with the removal of U(VI), Si, and Al from the solution. If no Si polymerization was observed, there was no U removal from the supernatant solution. Speciation modeling indicated that the dominant uranium species in the presence of bicarbonate were anionic uranyl carbonate complexes (UO2(CO3)2-2 and UO2(CO3)3-4) and in the absence of bicarbonate in the solution, U(VI) major species appeared as uranyl-hydroxide (UO2(OH)3- and UO2(OH)4-2) species. The model also predicted the formation of uranium solid phases. Uranyl carbonates as rutherfordine [UO2CO3], cejkaite [Na4(UO2)(CO3)3] and hydrated uranyl silicate phases as Na-boltwoodite [Na(UO2)(SiO4)·1.5H2O] were anticipated for most of the synthetic pore water compositions amended from medium (2.9 mM) to high (100 mM) bicarbonate concentrations.« less

Spatial variability and geochemistry of rare earth elements in soils from the largest uranium-phosphate deposit of Brazil.

PubMed

Cunha, Cleyton Saialy Medeiros; da Silva, Ygor Jacques Agra Bezerra; Escobar, Maria Eugenia Ortiz; do Nascimento, Clístenes Williams Araújo

2018-02-22

The Itataia uranium-phosphate deposit is the largest uranium reserve in Brazil. Rare earth elements (REEs) are commonly associated with phosphate deposits; however, there are no studies on the concentrations of REEs in soils of the Itataia deposit region. Thus, the objective of the research was to evaluate the concentration and spatial variability of REEs in topsoils of Itataia phosphate deposit region. In addition, the influence of soil properties on the geochemistry of REEs was investigated. Results showed that relatively high mean concentrations (mg kg -1 ) of heavy REEs (Gd 6.01; Tb 1.25; Ho 1.15; Er 4.05; Tm 0.64; Yb 4.61; Lu 0.65) were found in surface soils samples. Soil properties showed weak influence on the geochemical behavior of REEs in soils, except for the clay content. On the other hand, parent material characteristics, such as P and U, had strong influence on REEs concentrations. Spatial distribution patterns of REEs in soils are clearly associated with P and U contents. Therefore, geochemical surveys aiming at the delineation of ore-bearing zones in the region can benefit from our data. The results of this work reinforce the perspective for co-mining of P, U and REEs in this important P-U reserve.

Uniform deposition of uranium hexafluoride (UF6): Standardized mass deposits and controlled isotopic ratios using a thermal fluorination method.

PubMed

McNamara, Bruce K; O'Hara, Matthew J; Casella, Andrew M; Carter, Jennifer C; Addleman, R Shane; MacFarlan, Paul J

2016-07-01

We report a convenient method for the generation of volatile uranium hexafluoride (UF6) from solid uranium oxides and other U compounds, followed by uniform deposition of low levels of UF6 onto sampling coupons. Under laminar flow conditions, UF6 is shown to interact with surfaces within a fixed reactor geometry to a highly predictable degree. We demonstrate the preparation of U deposits that range between approximately 0.01 and 500ngcm(-2). The data suggest the method can be extended to creating depositions at the sub-picogramcm(-2) level. The isotopic composition of the deposits can be customized by selection of the U source materials and we demonstrate a layering technique whereby two U solids, each with a different isotopic composition, are employed to form successive layers of UF6 on a surface. The result is an ultra-thin deposit that bears an isotopic signature that is a composite of the two U sources. The reported deposition method has direct application to the development of unique analytical standards for nuclear safeguards and forensics. Further, the method allows access to very low atomic or molecular coverages of surfaces. Copyright © 2016 Elsevier B.V. All rights reserved.

Numerical analysis of single and multiple particles of Belchatow lignite dried in superheated steam

NASA Astrophysics Data System (ADS)

Zakrzewski, Marcin; Sciazko, Anna; Komatsu, Yosuke; Akiyama, Taro; Hashimoto, Akira; Kaneko, Shozo; Kimijima, Shinji; Szmyd, Janusz S.; Kobayashi, Yoshinori

2018-03-01

Low production costs have contributed to the important role of lignite in the energy mixes of numerous countries worldwide. High moisture content, though, diminishes the applicability of lignite in power generation. Superheated steam drying is a prospective method of raising the calorific value of this fuel. This study describes the numerical model of superheated steam drying of lignite from the Belchatow mine in Poland in two aspects: single and multi-particle. The experimental investigation preceded the numerical analysis and provided the necessary data for the preparation and verification of the model. Spheres of 2.5 to 30 mm in diameter were exposed to the drying medium at the temperature range of 110 to 170 °C. The drying kinetics were described in the form of moisture content, drying rate and temperature profile curves against time. Basic coal properties, such as density or specific heat, as well as the mechanisms of heat and mass transfer in the particular stages of the process laid the foundations for the model construction. The model illustrated the drying behavior of a single particle in the entire range of steam temperature as well as the sample diameter. Furthermore, the numerical analyses of coal batches containing particles of various sizes were conducted to reflect the operating conditions of the dryer. They were followed by deliberation on the calorific value improvement achieved by drying, in terms of coal ingredients, power plant efficiency and dryer input composition. The initial period of drying was found crucial for upgrading the quality of coal. The accuracy of the model is capable of further improvement regarding the process parameters.

Catalysts and process developments for two-stage liquefaction. Quarterly technical progress report, January 1, 1991--March 31, 1991, report No. 40

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

Cronauer, D.C.; Swanson, A.J.; Sajkowski, D.J.

Research under way in this project centers upon developing and evaluating catalysts and process improvements for coal liquefaction in the two-stage close-coupled catalytic process. Further experimentation was undertaken in a continuous flow unit with Black Thunder coal, where the primary goal was to determine the extent of decarboxylation and changes in the structure of the unconverted coal samples. The preliminary results indicated little conversion of the feed coal to THF solubles at 600{degrees}F, although the conversion did increase with increasing temperature up to 24% at 700{degrees}F. The level of decarboxylation was also low at the above reaction temperatures. Thus, presoakingmore » in a coal-derived solvent or even tetralin does not seem to be an effective means to achieve decarboxylation. Feedstock liquefaction studies were done with Martin Lake lignite in a two-stage continuous flow unit. Conversion to THF solubles was 82-87%. The Martin Lake lignite product was very light and no resid was produced. Sulfur levels in the product were low, although nitrogen levels were relatively high, requiring further processing by hydrotreating. An air-oxidized sample of Martin Lake lignite produced high oxygen containing resid at the expense of distillate, which clearly indicates that air oxidation of lignite is detrimental. The spent catalyst from the first stage was severely deactivated and generally, the spent catalysts from both stages were in worse condition than those from a previous run with Black Thunder coal. The completed testing results of Sandia`s NiMo/hydrous titanate oxide (NiMo/HTO) preparations are reported.« less

Chemical characterization and receptor modeling of PM10 in the surroundings of the opencast lignite mines of Western Macedonia, Greece.

PubMed

Samara, Constantini; Argyropoulos, George; Grigoratos, Theodoros; Kouras, Αthanasios; Manoli, Εvangelia; Andreadou, Symela; Pavloudakis, Fragkiskos; Sahanidis, Chariton

2018-05-01

The Western Macedonian Lignite Center (WMLC) in northwestern Greece is the major lignite center in the Balkans feeding four major power plants of total power exceeding 4 GW. Concentrations of PM 10 (i.e., particulate matters with diameters ≤10 μm) are the main concern in the region, and the high levels observed are often attributed to the activities related to power generation. In this study, the contribution of fugitive dust emissions from the opencast lignite mines to the ambient levels of PM 10 in the surroundings was estimated by performing chemical mass balance (CMB) receptor modeling. For this purpose, PM 10 samples were concurrently collected at four receptor sites located in the periphery of the mine area during the cold and the warm periods of the year (November-December 2011 and August-September 2012), and analyzed for a total of 26 macro- and trace elements and ionic species (sulfate, nitrate, chloride). The robotic chemical mass balance (RCMB) model was employed for source identification/apportionment of PM 10 at each receptor site using as inputs the ambient concentrations and the chemical profiles of various sources including the major mine operations, the fly ash escaping the electrostatic filters of the power plants, and other primary and secondary sources. Mean measured PM 10 concentrations at the different sites ranged from 38 to 72 μg m -3 . The estimated total contribution of mines ranged between 9 and 22% in the cold period increasing to 36-42% in the dry warm period. Other significant sources were vehicular traffic, biomass burning, and secondary sulfate and nitrate aerosol. These results imply that more efficient measures to prevent and suppress fugitive dust emissions from the mines are needed.

Condition-Based Conveyor Belt Replacement Strategy in Lignite Mines with Random Belt Deterioration

NASA Astrophysics Data System (ADS)

Blazej, Ryszard; Jurdziak, Leszek

2017-12-01

In Polish lignite surface mines, condition-based belt replacement strategies are applied in order to assure profitable refurbishment of worn out belts performed by external firms specializing in belt maintenance. In two of three lignite mines, staff asses belt condition subjectively during visual inspections. Only one mine applies specialized diagnostic device (HRDS) allowing objective magnetic evaluation of belt core condition in order to choose the most profitable moment for the dismantling of worn out belt segments from conveyors and sending them to the maintenance firm which provides their refurbishment. This article describes the advantages of a new diagnostic device called DiagBelt. It was developed at the Faculty of Geoengineering, Mining and Geology, Wroclaw University of Science and Technology. Economic gains from its application are calculated for the lignite mine and for the belt maintenance firm, taking into account random life (durability) of new and reconditioned belts (after the 1st and the 2nd refurbishment). Recursive calculations for following years allow the estimation of the length and costs of replaced, reconditioned and purchased belts on an annual basis, while the use of the Monte Carlo method allows the estimation of their variability caused by random deterioration of belts. Savings are obtained due to better selection of moments (times) for the replacement of belt segments and die to the possibility to qualify worn out belts for refurbishment without the need to remove their covers. In effect, increased belt durability and lowered share of waste belts (which were not qualified for reconditioning) create savings which can quickly cover expenditures on new diagnostic tools and regular belt inspections in the mine.

Removal of pharmaceuticals, perfluoroalkyl substances and other micropollutants from wastewater using lignite, Xylit, sand, granular activated carbon (GAC) and GAC+Polonite® in column tests - Role of physicochemical properties.

PubMed

Rostvall, Ande; Zhang, Wen; Dürig, Wiebke; Renman, Gunno; Wiberg, Karin; Ahrens, Lutz; Gago-Ferrero, Pablo

2018-06-15

This study evaluated the performance of five different sorbents (granular activated carbon (GAC), GAC + Polonite ® (GAC + P), Xylit, lignite and sand) for a set of 83 micropollutants (MPs) (pharmaceuticals, perfluoroalkyl substances (PFASs), personal care products, artificial sweeteners, parabens, pesticide, stimulants), together representing a wide range of physicochemical properties. Treatment with GAC and GAC + P provided the highest removal efficiencies, with average values above 97%. Removal rates were generally lower for Xylit (on average 74%) and lignite (on average 68%), although they proved to be highly efficient for a few individual MPs. The average removal efficiency for sand was only 47%. It was observed that the MPs behaved differently depending on their physicochemical properties. The physicochemical properties of PFASs (i.e. molecular weight, topological molecular surface area, log octanol water partition coefficient (K ow ) and distribution coefficient between octanol and water (log D)) were positively correlated to observed removal efficiency for the sorbents Xylit, lignite and sand (p < 0.05), indicating a strong influence of perfluorocarbon chain length and associated hydrophobic characteristics. In contrast, for the other MPs the ratio between apolar and polar surface area (SA/SP) was positively correlated with the removal efficiency, indicating that hydrophobic adsorption may be a key feature of their sorption mechanisms. GAC showed to be the most promising filter medium to improve the removal of MPs in on-site sewage treatment facilities. However, more studies are needed to evaluate the removal of MPs in field trials. Copyright © 2018 Elsevier Ltd. All rights reserved.

Development and demonstration of a lignite-pelletizing process. Phase II report

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

Not Available

1980-01-01

The current work began with scale-up of laboratory equipment to commercial size equipment. For this purpose, BCI used an existing pilot plant that had been assembled to pelletize and indurate taconite ore. BCI determined therewith that lignite pellets can be produced continuously on a pilot scale using the basic process developed in the laboratory. The resulting pellets were found to be similar to the laboratory pellets at equivalent binder compositions. Tests of product made during a 5-ton test run are reported. A 50-ton demonstration test run was made with the pilot plant. Pellet production was sustained for a two-week period.more » The lignite pelletizing process has, therefore, been developed to the point of demonstration in a 50-ton test. BCI has completed and cost estimated a conceptually designed 4000 TPD facility. BCI believes it has demonstrated a technically feasible process to agglomerate lignite by using an asphalt emulsion binder. Product quality is promising. Capital and operating costs appear acceptable to justify continuing support and development. The next step should focus on three areas: production development, process refinement, and cost reduction. For further development, BCI recommends consideration of a 5 to 10 ton/h pilot plant or a 20 to 40 ton/h module of a full sized plant, the lower first cost of the former being offset by the ability to incorporate the latter into a future production unit. Other specific recommendations are made for future study that could lead to process and cost improvements: Binder Formulation, disc Sizing, Drier Bed Depth, and Mixing Approach. Pellet use other than power plant fuel is considered.« less

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

Sozen, A.; Arcaklioglu, E.

The main goal of this study is to develop the energy sources estimation equations in order to estimate the future projections and make correct investments in Turkey using artificial neural network (ANN) approach. It is also expected that this study will be helpful in demonstrating energy situation of Turkey in amount of EU countries. Basic energy indicators such as population, gross generation, installed capacity, net energy consumption, import, export are used in input layer of ANN. Basic energy sources such as coal, lignite, fuel-oil, natural gas and hydro are in output layer. Data from 1975 to 2003 are used tomore » train. Three years (1981, 1994 and 2003) are only used as test data to confirm this method. Also, in this study, the best approach was investigated for each energy sources by using different learning algorithms (scaled conjugate gradient (SCG) and Levenberg-Marquardt (LM)) and a logistic sigmoid transfer function in the ANN with developed software. The statistical coefficients of multiple determinations (R{sup 2}-value) for training data are equal to 0.99802, 0.99918, 0.997134, 0.998831 and 0.995681 for natural gas, lignite, coal, hydraulic, and fuel-oil, respectively. Similarly, these values for testing data are equal to 0.995623, 0.999456, 0.998545, 0.999236, and 0.99002. The best approach was found for lignite by SCG algorithm with seven neurons so mean absolute percentage error (MAPE) is equal to 1.646753 for lignite. According to the results, the future projections of energy indicators using ANN technique have been obviously predicted within acceptable errors. Apart from reducing the whole time required, the importance of the ANN approach is possible to find solutions that make energy applications more viable and thus more attractive to potential users.« less

Modeling non-steady state radioisotope transport in the vadose zone--A case study using uranium isotopes at Pena Blanca, Mexico

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

Ku, T. L.; Luo, S.; Goldstein, S. J.

2009-06-01

Current models using U- and Th-series disequilibria to study radioisotope transport in groundwater systems mostly consider a steady-state situation. These models have limited applicability to the vadose zone (UZ) where the concentration and migratory behavior of radioisotopes in fluid are often transitory. We present here, as a first attempt of its kind, a model simulating the non-steady state, intermittent fluid transport in vadose layers. It provides quantitative constraints on in-situ migration of dissolved and colloidal radioisotopes in terms of retardation factor and rock-water interaction (or water transit) time. For uranium, the simulation predicts that intermittent flushing in the UZ leadsmore » to a linear relationship between reciprocal U concentration and {sup 234}U/{sup 238}U ratio in percolating waters, with the intercept and slope bearing information on the rates of dissolution and {alpha}-recoil of U isotopes, respectively. The general validity of the model appears to be borne out by the measurement of uranium isotopes in UZ waters collected at various times over a period during 1995-2006 from a site in the Pena Blanca mining district, Mexico, where the Nopal I uranium deposit is located. Enhanced {sup 234}U/{sup 238}U ratios in vadose-zone waters resulting from lengthened non-flushing time as prescribed by the model provide an interpretative basis for using {sup 234}U/{sup 238}U in cave calcites to reconstruct the regional changes in hydrology and climate. We also provide a theoretical account of the model's potential applications using radium isotopes.« less

Modeling non-steady state radioisotope transport in the vadose zone - A case study using uranium isotopes at Peña Blanca, Mexico

NASA Astrophysics Data System (ADS)

Ku, T. L.; Luo, S.; Goldstein, S. J.; Murrell, M. T.; Chu, W. L.; Dobson, P. F.

2009-10-01

Current models using U- and Th-series disequilibria to study radioisotope transport in groundwater systems mostly consider a steady-state situation. These models have limited applicability to the vadose zone (UZ) where the concentration and migratory behavior of radioisotopes in fluid are often transitory. We present here, as a first attempt of its kind, a model simulating the non-steady state, intermittent fluid transport in vadose layers. It provides quantitative constraints on in-situ migration of dissolved and colloidal radioisotopes in terms of retardation factor and rock-water interaction (or water transit) time. For uranium, the simulation predicts that intermittent flushing in the UZ leads to a linear relationship between reciprocal U concentration and 234U/ 238U ratio in percolating waters, with the intercept and slope bearing information on the rates of dissolution and α-recoil of U isotopes, respectively. The general validity of the model appears to be borne out by the measurement of uranium isotopes in UZ waters collected at various times over a period during 1995-2006 from a site in the Peña Blanca mining district, Mexico, where the Nopal I uranium deposit is located. Enhanced 234U/ 238U ratios in vadose-zone waters resulting from lengthened non-flushing time as prescribed by the model provide an interpretative basis for using 234U/ 238U in cave calcites to reconstruct the regional changes in hydrology and climate. We also provide a theoretical account of the model's potential applications using radium isotopes.

Compositions and methods for removing arsenic in water

DOEpatents

Gadgil, Ashok Jagannth [El Cerrito, CA

2011-02-22

Compositions and methods and for contaminants from water are provided. The compositions comprise ferric hydroxide and ferric oxyhydride coated substrates for use in removing the contaminant from the water. Contacting water bearing the contaminant with the substrates can substantially reduce contaminant levels therein. Methods of oxidizing the contaminants in water to facilitate their removal by the ferric hydroxide and ferric oxyhydride coated substrates are also provided. The contaminants include, but are not limited to, arsenic, selenium, uranium, lead, cadmium, nickel, copper, zinc, chromium and vanadium, their oxides and soluble salts thereof.

Method and apparatus for drilling horizontal holes in geological structures from a vertical bore

DOEpatents

Summers, David A.; Barker, Clark R.; Keith, H. Dean

1982-01-01

This invention is directed to a method and apparatus for drilling horizontal holes in geological strata from a vertical position. The geological structures intended to be penetrated in this fashion are coal seams, as for in situ gasification or methane drainage, or in oil-bearing strata for increasing the flow rate from a pre-existing well. Other possible uses for this device might be for use in the leaching of uranium ore from underground deposits or for introducing horizontal channels for water and steam injections.

Chemical data and statistical interpretations for rocks and ores from the Ranger uranium mine, Northern Territory, Australia

USGS Publications Warehouse

Nash, J. Thomas; Frishman, David

1983-01-01

Analytical results for 61 elements in 370 samples from the Ranger Mine area are reported. Most of the rocks come from drill core in the Ranger No. 1 and Ranger No. 3 deposits, but 20 samples are from unmineralized drill core more than 1 km from ore. Statistical tests show that the elements Mg, Fe, F, Be, Co, Li, Ni, Pb, Sc, Th, Ti, V, CI, As, Br, Au, Ce, Dy, La Sc, Eu, Tb, Yb, and Tb have positive association with uranium, and Si, Ca, Na, K, Sr, Ba, Ce, and Cs have negative association. For most lithologic subsets Mg, Fe, Li, Cr, Ni, Pb, V, Y, Sm, Sc, Eu, and Yb are significantly enriched in ore-bearing rocks, whereas Ca, Na, K, Sr, Ba, Mn, Ce, and Cs are significantly depleted. These results are consistent with petrographic observations on altered rocks. Lithogeochemistry can aid exploration, but for these rocks requires methods that are expensive and not amenable to routine use.

Natural thorium resources and recovery: Options and impacts

USGS Publications Warehouse

Ault, Timothy; Van Gosen, Bradley S.; Krahn, Steven; Croff, Allen

2016-01-01

This paper reviews the front end of the thorium fuel cycle, including the extent and variety of thorium deposits, the potential sources of thorium production, and the physical and chemical technologies required to isolate and purify thorium. Thorium is frequently found within rare earth element–bearing minerals that exist in diverse types of mineral deposits, often in conjunction with other minerals mined for their commercial value. It may be possible to recover substantial quantities of thorium as a by-product from active titanium, uranium, tin, iron, and rare earth mines. Incremental physical and chemical processing is required to obtain a purified thorium product from thorium minerals, but documented experience with these processes is extensive, and incorporating thorium recovery should not be overly challenging. The anticipated environmental impacts of by-product thorium recovery are small relative to those of uranium recovery since existing mining infrastructure utilization avoids the opening and operation of new mines and thorium recovery removes radionuclides from the mining tailings.

Radioactivity and uranium content of the Sharon Springs member of the Pierre shale and associated rocks in western Kansas and eastern Colorado

USGS Publications Warehouse

Landis, Edwin R.

1955-01-01

As a part of the Geological Survey's program of investigating uranium-bearing carbonaceous rocks on behalf of the Division of Raw Materials of the U.S. Atomic Energy Commission, a reconnaissance of the Sharon Springs member of the Pierre shale in western Kansas and eastern Colorado was conducted during 1954. The Sharon Springs member of the Pierre shale and its lateral equivalents ranges from 155 to about 500 feet in thickness and generally contains about 0.001 percent uranium, but some beds contain larger amounts. A 6-foot thick shale bed in Cheyenne County, Colo., contains about 0.006 percent uranium, a 4 1/2-foot thick sequence of beds in Crowley County, Colo., is estimated to contain between 0.004 and 0.005 percent uranium, and a 3 1/2-foot thick sequence of beds in Kiowa County, Colo., contains about 0.004 percent uranium. At several outcrop localities, sequences of beds as much as 9 1/2 feet thick contain about 0.003 percent uranium. Data from wells indicate that the 4 1/2-foot thick sequence of beds in Crowley County, Colo., may have a lateral extent of at least 5 1/2 miles. A gamma-ray log of a well in Yuma County, Colo., indicates the presence of a sequence of beds 66 feet thick which contains 0.005 to 0.010 percent equivalent uranium. No definite pattern of areal distribution of radioactivity and uranium content in the Sharon Springs is indicated by available data. Lateral variation in uranium content of individual beds was not noted in outcrops, which seldom extend more than 150 feet, but subsurface data from gamma-ray logs of wells indicate that both the maximum radioactivity and the thickness of radioactive beds are variable within distances of a few miles. Vertical variation in radioactivity and uranium content of the more radioactive beds is usually abrupt, but in the rocks as a whole the range of uranium content is so small that large variations in content are absent. In most of the gamma-ray logs examined there is only part of the sequence of rocks comprising the Pierre shale and Niobrara formation that exhibits radioactivity in excess of the average radioactivity of the two formations. Comparison of features of gamma-ray logs of wells in north-eastern Colorado suggests that the most radioactive part referred to above is a laterally correlatable sequence of beds. The stratigraphic position of the radioactive unit relative to the Pierre shale-Niobrara formation contact in oil industry scout reports, as identified from electric logs and wells, is variable within short distances. This may indicate that some of the Pierre-Niobrara contacts picked from electric logs may not correspond to the boundary that would be selected by examination of the rocks themselves, or may indicate that there is a facies relationship between teh lowermost part of the Pierre shale and the uppermost part of the Niobrara formation.

Exploring the effect of oxygen-containing functional groups on the water-holding capacity of lignite.

PubMed

Liu, Jie; Jiang, Xiangang; Cao, Yu; Zhang, Chen; Zhao, Guangyao; Zhao, Maoshuang; Feng, Li

2018-05-07

Graphene oxide with different degrees of oxidation was prepared and selected as a model compound of lignite to study quantitatively, using both experiment and theoretical calculation methods, the effect on water-holding capacity of oxygen-containing functional groups. The experimental results showed that graphite can be oxidized, and forms epoxy groups most easily, followed by hydroxyl and carboxyl groups. The prepared graphene oxide forms a membrane-state as a single layer structure, with an irregular surface. The water-holding capacity of lignite increased with the content of oxygen-containing functional groups. The influence on the configuration of water molecule clusters and binding energy of water molecules of different oxygen-containing functional groups was calculated by density functional theory. The calculation results indicated that the configuration of water molecule clusters was totally changed by oxygen-containing functional groups. The order of binding energy produced by oxygen-containing functional groups and water molecules was as follows: carboxyl > edge phenol hydroxyl >epoxy group. Finally, it can be concluded that the potential to form more hydrogen bonds is the key factor influencing the interaction energy between model compounds and water molecules.

Chemical mass balance source apportionment of TSP in a lignite-burning area of Western Macedonia, Greece

NASA Astrophysics Data System (ADS)

Samara, Constantini

Total suspended particle mass concentrations (TSP) were determined in the Kozani-Ptolemais-Florina basin (western Macedonia, Greece), an area with intensive lignite burning for power generation. The study was conducted over a 1-year period (November 2000-November 2001) at 10 receptor sites located at variable distances from the power plants. Ambient TSP samples were analyzed for 27 major, minor and trace elements. Particulate emissions were also collected from a variety of sources including fly ash, lignite dust, automobile traffic, domestic heating, and open-air burning of agricultural biomass and refuse, and analyzed for the same chemical components. Ambient and source chemical profiles were used for source identification and apportionment of TSP by employing a chemical mass balance (CMB) receptor model. Diesel burning in vehicular traffic and in the power plants for generator start up was found to be the major contributor to ambient TSP levels at all 10 sites. Other sources with significant contributions were domestic coal burning, vegetative burning (wood combustion and agricultural burns) and refuse open-air burning. Fly ash escaping the electrostatic precipitators of the power plants was a minor contributor to ambient TSP.

Land movement monitoring at the Mavropigi lignite mine using spaceborne D-InSAR

NASA Astrophysics Data System (ADS)

Papadaki, Eirini; Tripolitsiotis, Achilleas; Steiakakis, Chrysanthos; Agioutantis, Zacharias; Mertikas, Stelios; Partsinevelos, Panagiotis; Schilizzi, Pavlos

2013-08-01

This paper examines the capability of remote sensing radar interferometry to monitor land movements, as it varies with time, in areas close to open pit lignite mines. The study area is the "Mavropigi" lignite mine in Ptolemais, Northern Greece; whose continuous operation is of vital importance to the electric power supply of Greece. The mine is presently 100-120m deep while horizontal and vertical movements have been measured in the vicinity of the pit. Within the mine, ground geodetic monitoring has revealed an average rate of movement amounting to 10-20mm/day at the southeast slopes. In this work, differential interferometry (DInSAR), using 19 Synthetic Aperture Radar (SAR) images of ALOS satellite, has been applied to monitor progression of land movement caused my mining within the greater area of "Mavropigi" region. The results of this work show that DInSAR can be used effectively to capture ground movement information, well before signs of movements can be observed visually in the form of imminent fissures and tension cracks. The advantage of remote sensing interferometry is that it can be applied even in inaccessible areas where monitoring with ground equipment is either impossible or of high-cost (large areas).

Petrographic and anatomical characteristics of plant material from two peat deposits of Holocene and Miocene age, Kalimantan, Indonesia

USGS Publications Warehouse

Moore, T.A.; Hilbert, R.E.

1992-01-01

Samples from two peat-forming environments of Holocene and Miocene age in Kalimantan (Borneo), Indonesia, were studied petrographically using nearly identical sample preparation and microscopic methodologies. Both deposits consist of two basic types of organic material: plant organs/tissues and fine-grained matrix. There are seven predominant types of plant organs and tissues: roots possessing only primary growth, stems possessing only primary growth, leaves, stems/roots with secondary growth, secondary xylem fragments, fragments of cork cells, and macerated tissue of undetermined origin. The fine-grained matrix consists of fragments of cell walls and cell fillings, fungal remains, spores and pollen grains, and resin. Some of the matrix material does not have distinct grain boundaries (at ??500) and this material is designated amorphous matrix. The major difference between the Holocene peat and Miocene lignite in reflected light, oil immersion is a loss of red coloration in the cell walls of tissue in the lignite, presumably due to loss of cellulosic compounds. In addition, cortex and phloem tissue (hence primary roots and stems) are difficult to recognize in the lignite, probably because these large, thin-walled tissues are more susceptible to microbial degradation and compaction. Particle size in both peat and lignite samples display a bimodal distribution when measurements are transformed to a - log2 or phi (??), scale. Most plant parts have modes of 2-3?? (0.25 - 0.125 mm), whereas the finer-grained particulate matrix has modes of 7-9?? (0.008-0.002 mm). This similarity suggest certain degradative processes. The 2-3?? range may be a "stable" size for plant parts (regardless of origin) because this is a characteristics of a substrate which is most suitable for plant growth in peat. The finer-grained matrix material (7-9??) probably results from fungal decay which causes plant material to weaken and with slight physical pressure to shatter into its component parts, i.e. fragments of cell walls and fillings. The absence of differences in particle size between the peat and lignite also indicate little compaction of organic components; rather an extreme loss in water content and pore space has occurred from between the particles of organic material. ?? 1992.

Geology of the Ralston Buttes district, Jefferson County, Colorado: a preliminary report

USGS Publications Warehouse

Sheridan, Douglas M.; Maxwell, Charles H.; Albee, Arden L.; Van Horn, Richard

1956-01-01

The Ralston Buttes district in Jefferson County is one of the most significant new uranium districts located east of the Continental Divide in Colorado. The district is east of the Colorado Front Range mineral belt, along the east front of the range. From November 1953 through October 1956, about 10,000 tons of uranium ore, much of which was high-grade pitchblende-bearing vein material, was shipped from the district. The ore occurs in deposits that range in size from bodies containing less than 50 tons to ore shoots containing over 1,000 tons. The only other mining activity in the area has been a sporadic production of beryl, feldspar, and scrap mica from Precambrian pegmatites, and quarrying of dimension stone, limestone, and clay from sedimentary rocks. Most of the Ralston Buttes district consists of complexly folded Precambrian metamorphic and igneous rocks - gneiss, schist, quartzite, amphibolite, and granodiorite. Paleozoic and Mesozoic sedimentary rocks crop out in the northeastern part of the district. These rocks are cut by northwesterly-trending fault systems of Laramide age and by small bodies of intrusive rocks that are Tertiary in age. The typical uranium deposits in the district are hydrothermal veins occupying openings in Laramide fault breccias or related fractures that cut the Precambrian rocks. Pitchblende and lesser amounts of secondary uranium minerals are associated with sparse base-mental sulfides in a gangue of carbonate minerals, potash feldspar, and, more rarely, quartz. Less common types of deposits consist of pitchblende and secondary uranium minerals that occupy fractures cutting pegmatites and quartz veins. The uranium deposits are concentrated in two areas, the Ralston Creek area and the Golden Gate Canyon area. The deposits in the Ralston Creek area are located along the Rogers fault system, and the deposits in the Golden Gate Canyon area are along the Hurricane Hill fault system. Two geologic factors were important to the localization of the uranium deposits: (1) favorable structural environment and (2) favorable host rocks. The deposits in each of the two major areas are located where a northwesterly-trending Laramide fault system splits into a complex network of faults. Also, most of the deposits appear to be localized where the faults cut Precambrian rocks rich in hornblende, biotite, or garnet and biotite. The ore controls recognized in this relatively new uranium district may have wider application in areas of similar geology elsewhere in the Front Range.

Assessment of the Coal-Bed Gas Total Petroleum System in the Cook Inlet-Susitna region, south-central Alaska

USGS Publications Warehouse

Rouse, William A.; Houseknecht, David W.

2012-01-01

The Cook Inlet-Susitna region of south-central Alaska contains large quantities of gas-bearing coal of Tertiary age. The U.S. Geological Survey in 2011 completed an assessment of undiscovered, technically recoverable coal-bed gas resources underlying the Cook Inlet-Susitna region based on the total petroleum system (TPS) concept. The Cook Inlet Coal-Bed Gas TPS covers about 9,600,000 acres and comprises the Cook Inlet basin, Matanuska Valley, and Susitna lowland. The TPS contains one assessment unit (AU) that was evaluated for coal-bed gas resources between 1,000 and 6,000 feet in depth over an area of about 8,500,000 acres. Coal beds, which serve as both the source and reservoir for natural gas in the AU, were deposited during Paleocene-Pliocene time in mires associated with a large trunk-tributary fluvial system. Thickness of individual coal beds ranges from a few inches to more than 50 feet, with cumulative coal thickness of more than 800 feet in the western part of the basin. Coal rank ranges from lignite to subbituminous, with vitrinite reflectance values less than 0.6 percent throughout much of the AU. The AU is considered hypothetical because only a few wells in the Matanuska Valley have tested the coal-bed reservoirs, so the use of analog coal-bed gas production data was necessary for this assessment. In order to estimate reserves that might be added in the next 30 years, coal beds of the Upper Fort Union Formation in the Powder River Basin of Wyoming and Montana were selected as the production analog for Tertiary coal beds in the Cook Inlet-Susitna region. Upper Fort Union coal beds have similar rank (lignite to subbituminous), range of thickness, and coal-quality characteristics as coal beds of the Tertiary Kenai Group. By use of this analog, the mean total estimate of undiscovered coal-bed gas in the Tertiary Coal-Bed Gas AU is 4.674 trillion cubic feet (TCF) of gas.

Biogeochemical aspects of uranium mineralization, mining, milling, and remediation

USGS Publications Warehouse

Campbell, Kate M.; Gallegos, Tanya J.; Landa, Edward R.

2015-01-01

Natural uranium (U) occurs as a mixture of three radioactive isotopes: 238U, 235U, and 234U. Only 235U is fissionable and makes up about 0.7% of natural U, while 238U is overwhelmingly the most abundant at greater than 99% of the total mass of U. Prior to the 1940s, U was predominantly used as a coloring agent, and U-bearing ores were mined mainly for their radium (Ra) and/or vanadium (V) content; the bulk of the U was discarded with the tailings (Finch et al., 1972). Once nuclear fission was discovered, the economic importance of U increased greatly. The mining and milling of U-bearing ores is the first step in the nuclear fuel cycle, and the contact of residual waste with natural water is a potential source of contamination of U and associated elements to the environment. Uranium is mined by three basic methods: surface (open pit), underground, and solution mining (in situ leaching or in situ recovery), depending on the deposit grade, size, location, geology and economic considerations (Abdelouas, 2006). Solid wastes at U mill tailings (UMT) sites can include both standard tailings (i.e., leached ore rock residues) and solids generated on site by waste treatment processes. The latter can include sludge or “mud” from neutralization of acidic mine/mill effluents, containing Fe and a range of coprecipitated constituents, or barium sulfate precipitates that selectively remove Ra (e.g., Carvalho et al., 2007). In this chapter, we review the hydrometallurgical processes by which U is extracted from ore, the biogeochemical processes that can affect the fate and transport of U and associated elements in the environment, and possible remediation strategies for site closure and aquifer restoration.This paper represents the fourth in a series of review papers from the U.S. Geological Survey (USGS) on geochemical aspects of UMT management that span more than three decades. The first paper (Landa, 1980) in this series is a primer on the nature of tailings and radionuclide mobilization from them. The second paper (Landa, 1999) includes coverage of research carried out under the U.S. Department of Energy’s Uranium Mill Tailings Remedial Action Program (UMTRA). The third paper (Landa, 2004) reflects the increased focus of researchers on biotic effects in UMT environs. This paper expands the focus to U mining, milling, and remedial actions, and includes extensive coverage of the increasingly important alkaline in situ recovery and groundwater restoration.

Grain growth in uranium nitride prepared by spark plasma sintering

NASA Astrophysics Data System (ADS)

Johnson, Kyle D.; Lopes, Denise Adorno

2018-05-01

Uranium mononitride (UN) has long been considered a potential high density, high performance fuel candidate for light water reactor (LWR) and fast reactor (FR) applications. However, deployability of this fuel has been limited by the notable resistance to sintering and subsequent difficulty in producing a desirable microstructure, the high costs associated with 15N enrichment, as well as the known proclivity to oxidation and interaction with steam. In this study, the stimulation of grain growth in UN pellets sintered using SPS has been investigated. The results reveal that by using SPS and controlling temperature, time, and holding pressure, grain growth can be stimulated and controlled to produce a material featuring both a desired porosity and grain size, at least within the range of interest for nuclear fuel candidates. Grain sizes up to 31 μm were obtained using temperatures of 1650 °C and hold times of 15 min. Evaluation by EBSD reveal grain rotation and coalescence as the dominant mechanism in grain growth, which is suppressed by the application of higher external pressure. Moreover, complete closure of the porosity of the material was observed at relative densities of 96% TD, resulting in a material with sufficient porosity to accommodate LWR burnup. These results indicate that a method exists for the economic fabrication of an 15N-bearing uranium mononitride fuel with favorable microstructural characteristics compatible with use in a light water-cooled nuclear reactor.

Spectral pathways for exploration of secondary uranium: An investigation in the desertic tracts of Rajasthan and Gujarat, India

NASA Astrophysics Data System (ADS)

Bharti, Rishikesh; Kalimuthu, R.; Ramakrishnan, D.

2015-10-01

This study aims at identifying potential zones of secondary uranium enrichment using hyperspectral remote sensing, γ-ray spectrometry, fluorimetry and geochemical techniques in the western Rajasthan and northern Gujarat, India. The investigated area has suitable source rocks, conducive past-, and present-climate that can facilitate such enrichment. This enrichment process involves extensive weathering of uranium bearing source rocks, leaching of uranyl compounds in groundwater, and their precipitation in chemical deltas along with duricrusts like calcretes and gypcretes. Spatial distribution of groundwater calcretes (that are rich in Mg-calcite) and gypcretes (that are rich in gypsum) along palaeochannels and chemical deltas were mapped using hyperspectral remote sensing data based on spectral absorptions in 1.70 μm, 2.16 μm, 2.21 μm, 2.33 μm, 2.44 μm wavelength regions. Subsequently based on field radiometric survey, zones of U anomalies were identified and samples of duricrusts and groundwater were collected for geochemical analyses. Anomalous concentration of U (2345.7 Bq/kg) and Th (142.3 Bq/kg) are observed in both duricrusts and groundwater (U-1791 μg/l, Th-34 μg/l) within the palaeo-delta and river confluence. The estimated carnotite Solubility Index also indicates the secondary enrichment of U and the likelihood of occurrence of an unconventional deposit.

Reuse of thermosetting plastic waste for lightweight concrete.

PubMed

Panyakapo, Phaiboon; Panyakapo, Mallika

2008-01-01

This paper presents the utilization of thermosetting plastic as an admixture in the mix proportion of lightweight concrete. Since this type of plastic cannot be melted in the recycling process, its waste is expected to be more valuable by using as an admixture for the production of non-structural lightweight concrete. Experimental tests for the variation of mix proportion were carried out to determine the suitable proportion to achieve the required properties of lightweight concrete, which are: low dry density and acceptable compressive strength. The mix design in this research is the proportion of plastic, sand, water-cement ratio, aluminum powder, and lignite fly ash. The experimental results show that the plastic not only leads to a low dry density concrete, but also a low strength. It was found that the ratio of cement, sand, fly ash, and plastic equal to 1.0:0.8:0.3:0.9 is an appropriate mix proportion. The results of compressive strength and dry density are 4.14N/mm2 and 1395 kg/m3, respectively. This type of concrete meets most of the requirements for non-load-bearing lightweight concrete according to ASTM C129 Type II standard.

Exploration of cultivable fungal communities in deep coal-bearing sediments from ∼1.3 to 2.5 km below the ocean floor.

PubMed

Liu, Chang-Hong; Huang, Xin; Xie, Tian-Ning; Duan, Ning; Xue, Ya-Rong; Zhao, Tan-Xi; Lever, Mark A; Hinrichs, Kai-Uwe; Inagaki, Fumio

2017-02-01

Although subseafloor sediments are known to harbour a vast number of microbial cells, the distribution, diversity, and origins of fungal populations remain largely unexplored. In this study, we cultivated fungi from 34 of 47 deep coal-associated sediment samples collected at depths ranging from 1289 to 2457 m below the seafloor (mbsf) off the Shimokita Peninsula, Japan (1118 m water depth). We obtained a total of 69 fungal isolates under strict contamination controls, representing 61 Ascomycota (14 genera, 23 species) and 8 Basidiomycota (4 genera, 4 species). Penicillium and Aspergillus relatives were the most dominant genera within the Ascomycetes, followed by the members of genera Cladosporium, Hamigera, Chaetomium, Eutypella, Acremonium, Aureobasidium, Candida, Eurotium, Exophiala, Nigrospora, Bionectria and Pseudocercosporella. Four Basidiomycota species were identified as genera Schizophyllum, Irpex, Bjerkandera and Termitomyces. Among these isolates, Cladosporium sphaerospermum and Aspergillus sydowii relatives were isolated from a thin lignite coal-sandstone formation at 2457 mbsf. Our results indicate that these cultivable fungal populations are indigenous, originating from past terrigenous environments, which have persisted, possibly as spores, through ∼20 million years of depositional history. © 2017 Society for Applied Microbiology and John Wiley & Sons Ltd.

Trace elements reconnaissance investigations in New Mexico and adjoining states in 1951

USGS Publications Warehouse

Bachman, George O.; Read, Charles B.

1952-01-01

In the summer and fall of 1951, a reconnaissance search was made in New Mexico and adjacent states for uranium in coal and carbonaceous shale, chiefly of Mesozoic age, and black marine shale of Paleozoic age. Tertiary volcanic rocks, considered to be a possible source for uranium in the coal and associated rocks, were examined where the volcanic rocks were near coal-bearing strata. Uranium in possibly commercial amounts was found at La Ventana Mesa, Sandoval County, New Mexico. Slightly uranifeous coal and carbonaceous shale were found near San Ysidro, Sandoval County, and on Beautiful Mountain, San Juan County, all in New Mexico, and at Keams Canyon, Navajo County, and near Tuba City, Coconino County, in Arizona. Except for La Ventana deposit, none appeared to be of economic importance at the time this report was written, but additional reconnaissance investigations have been underway this field season, in the area where the deposits occur. Marine black shale of Sevonian age was examined in Otero and Socorro Counties, New Mexico and Gila County, Arizona. Mississippian black shale in Socorro County and Pennsylvanian black shale in Taos County, New Mexico were also tested. Equivalent uranium content of samples of these shales did not exceed 0.004 percent. Rhyolitic tuff from the Mount Taylor region is slightly radioactive as is the Bandelier tuff in the Nacimiento region and in the Jemez Plateau. Volcanic rocks in plugs and dikes in the northern Chuska Mountains and to the north in New Mexico as well as in northeastern Arizona and southeastern Utah are slightly radioactive. Coal and carbonaceous rocks in the vicinity of these and similar intrusions are being examined.

Isotopically exchangeable organic hydrogen in coal relates to thermal maturity and maceral composition

USGS Publications Warehouse

Mastalerz, Maria; Schimmelmann, A.

2002-01-01

Hydrogen isotopic exchangeability (Hex) and ??Dn values of non-exchangeable organic hydrogen were investigated in coal kerogens ranging in rank from lignite to graphite. The relative abundance of Hex is highest in lignite with about 18% of total hydrogen being exchangeable, and decreases to around 2.5% in coals with Ro of 1.7 to ca. 5.7%. At Still higher rank (Ro > 6%), Hex increases slightly, although the abundance of total hydrogen decreases. ??Dn is influenced by original biochemical D/H ratios and by thermal maturation in contact with water. Therefore, ??Dn does not show an overall consistent trend with maturity. ?? 2002 Elsevier Science Ltd. All rights reserved.

Method for preparing hydride configurations and reactive metal surfaces

DOEpatents

Silver, Gary L.

1988-08-16

A method for preparing highly hydrogen-reactive surfaces on metals which normally require substantial heating, high pressures, or an extended induction period, which involves pretreatment of said surfaces with either a non-oxidizing acid or hydrogen gas to form a hydrogen-bearing coating on said surfaces, and subsequently heating said coated metal in the absence of moisture and oxygen for a period sufficient to decompose said coating and cooling said metal to room temperature. Surfaces so treated will react almost instantaneously with hydrogen gas at room temperature and low pressure. The method is particularly applicable to uranium, thorium, and lanthanide metals.

Structural degradation of Thar lignite using MW1 fungal isolate: optimization studies

USGS Publications Warehouse

Haider, Rizwan; Ghauri, Muhammad A.; Jones, Elizabeth J.; Orem, William H.; SanFilipo, John R.

2015-01-01

Biological degradation of low-rank coals, particularly degradation mediated by fungi, can play an important role in helping us to utilize neglected lignite resources for both fuel and non-fuel applications. Fungal degradation of low-rank coals has already been investigated for the extraction of soil-conditioning agents and the substrates, which could be subjected to subsequent processing for the generation of alternative fuel options, like methane. However, to achieve an efficient degradation process, the fungal isolates must originate from an appropriate coal environment and the degradation process must be optimized. With this in mind, a representative sample from the Thar coalfield (the largest lignite resource of Pakistan) was treated with a fungal strain, MW1, which was previously isolated from a drilled core coal sample. The treatment caused the liberation of organic fractions from the structural matrix of coal. Fungal degradation was optimized, and it showed significant release of organics, with 0.1% glucose concentration and 1% coal loading ratio after an incubation time of 7 days. Analytical investigations revealed the release of complex organic moieties, pertaining to polyaromatic hydrocarbons, and it also helped in predicting structural units present within structure of coal. Such isolates, with enhanced degradation capabilities, can definitely help in exploiting the chemical-feedstock-status of coal.

Rehabilitation of a lignite mine-disturbed area in the Indian Desert

USGS Publications Warehouse

Sharma, K.D.; Kumar, P.; Gough, L.P.; SanFilipo, J.R.

2004-01-01

Extensive lignite mining in the Indian (Thar) Desert commenced within the past decade. Accompanying extraction of this valuable resource there have been visible, important environmental impacts. The resultant land degradation has prompted concern from both public and regulatory bodies. This research assesses the success of rehabilitation plans implemented to revegetate a lignite mine-disturbed area, near the village of Giral in western Rajasthan State. Rehabilitation success was achieved within the environmental constraints of this northwest Indian hot-desert ecosystem using a combination of: (1) backfilling (abandoned pits) with minespoil and of covering the backfilled-surfaces with fresh topsoil to a thickness of about 0??30 m; (2) use of micro-catchment rainwater harvesting (MCWH) technique; (3) soil profile modification approaches; (4) plant establishment methodologies; and (5) the selection of appropriate germplasm material (trees, shrubs and grasses). Preliminary results indicate that the resulting vegetative cover will be capable of self-perpetuation under natural conditions while at the same time meeting the land-use requirements of the local people. The minespoil is alkaline in nature and has high electrical conductance. The average content of organic carbon, N, P and K is lower than in the regional topsoil. However, the concentration of Ca, Mg, Na and total S in the minespoil is much higher than in the topsoil. Further, the spoil material has no biological activity. Enhanced plant growth was achieved in MCWH plots, compared to control plots, where minespoil moisture storage was improved by 18-43 per cent. The rehabilitation protocol used at the site appears to have been successful because, in addition to the planted species, desirable native invasive species have become established. This study developed methods for the rehabilitation of lignite mine-disturbed areas and has also resulted in an understanding of rehabilitation processes in arid regions with an emphasis on the long-term monitoring of rehabilitation success. ?? 2004 John Wiley and Sons, Ltd.

Comparative Study on Synergetic Degradation of a Reactive Dye Using Different Types of Fly Ash in Combined Adsorption and Photocatalysis

NASA Astrophysics Data System (ADS)

Giri Babu, P. V. S.; Swaminathan, G.

2016-09-01

A comprehensive study was carried out on four different fly ashes used as a catalyst for the degradation of Acid Red 1 using ultraviolet rays. These fly ashes are collected from different thermal power stations located at various places in India and having different chemical compositions. Three fly ashes are from lignite-based thermal power plants, and one is from the coal-based power plant. One fly ash is classified as Class F, two fly ashes are classified as Class C and remaining one is not conforming to ASTM C618 classification. X-Ray Fluorescence analysis was used to identify the chemical composition of fly ashes and SiO2, Al2O3, CaO, Fe2O3 and TiO2 were found to be the major elements present in different proportions. Various analysis were carried out on all the fly ashes like Scanning Electron Microscopy to identify the microphysical properties, Energy Dispersive X-Ray spectroscopy to quantify the elements present in the catalyst and X-Ray Diffraction to identify the catalyst phase analysis. The radical generated during the reaction was identified by Electron paramagnetic resonance spectroscopy. The parameters such as initial pH of the dye solution, catalyst dosage and initial dye concentration which influence the dye degradation efficiency were studied and optimised. In 60 min duration, the dye degradation efficiency at optimum parametric values of pH 2.5, initial dye concentration of 10 mg/L and catalyst dosage of 1.0 g/L using various fly ashes, i.e., Salam Power Plant, Barmer Lignite Power Plant, Kutch Lignite Power Plant and Neyveli Lignite Thermal Power plant (NLTP) were found to be 40, 60, 67 and 95 % respectively. The contribution of adsorption alone was 18 % at the above mentioned optimum parametric values. Among the above four fly ash NLTP fly ashes proved to be most efficient.

Determining the area of influence of depression cone in the vicinity of lignite mine by means of triangle method and LANDSAT TM/ETM+ satellite images.

PubMed

Zawadzki, Jarosław; Przeździecki, Karol; Miatkowski, Zygmunt

2016-01-15

Problems with lowering of water table are common all over the world. Intensive pumping of water from aquifers for consumption, irrigation, industrial or mining purposes often causes groundwater depletion and results in the formation of cone of depression. This can severely decrease water pressure, even over vast areas, and can create severe problems such as degradation of agriculture or natural environment sometimes depriving people and animals of water supply. In this paper, the authors present a method for determining the area of influence of a groundwater depression cone resulting from prolonged drainage, by means of satellite images in optical, near infrared and thermal infrared bands from TM sensor (Thematic Mapper) and ETM+ sensor (Enhanced Thematic Mapper +) placed on Landsat 5 and Landsat 7 satellites. The research area was Szczercowska Valley (Pol. Kotlina Szczercowska), Central Poland, located within a range of influence of a groundwater drainage system of the lignite coal mine in Belchatow. It is the biggest lignite coal mine in Poland and one of the largest in Europe exerting an enormous impact on the environment. The main method of satellite data analysis for determining soil moisture, was the so-called triangle method. This method, based on TVDI (Temperature Vegetation Dryness Index) was supported by additional spatial analysis including ordinary kriging used in order to combine fragmentary information obtained from areas covered by meadows. The results obtained are encouraging and confirm the usefulness of the triangle method not only for soil moisture determination but also for assessment of the temporal and spatial changes in the area influenced by the groundwater depression cone. The range of impact of the groundwater depression cone determined by means of above-described remote sensing analysis shows good agreement with that determined by ground measurements. The developed satellite method is much faster and cheaper than in-situ measurements, and allows for systematic monitoring of the vast area in the vicinity of Belchatow lignite mine. Besides, this method could be useful as a helper in in-situ measurement allowing a significant reduction of the number of in-situ measurements by performing them only within problematic areas. Hence, the triangle method can be used as an effective supplement to field measurements. Although the research area is located in Poland, in the vicinity of lignite mine, the method of observation of depression cones provided in this study is universal and effective, and therefore could also be useful to an international audience. Copyright © 2015 Elsevier Ltd. All rights reserved.

The increase of the fertility of soils using the liquid organic fertilizers and fertilizers based on sugar-beet wastes.

NASA Astrophysics Data System (ADS)

Vyborova, Oxana

2010-05-01

The fertility of soil is a capacity for ensuring plants by water, nutrients, air and capacity for making optimal conditions for growth and development of plants. The result of it is a yield. The main characteristic of fertility of soil is maintenance of humus. The humus is important part of organic matter. The supporting of soil fertility is impossible by traditional methods. The amount of receiving mineral fertilizers in agriculture will not increase in future, because mineral fertilizers are very expensive. The mineral fertilizers don't influence on maintenance of total amount of humus in soil and improve the circulation of nutrients. Every hectare of fields have to receive no less than 8-10 tons of organic fertilizers, therefore we will have self-supporting balance of humus and the fertility of soils will be increasing. Consequently we are looking for new types of organic materials and we include them in modern agro technologies. One of them is an organomineral fertilizer (lignitic materials). The humic chemicals in the form of lignitic materials of natrium, potassium and ammonium are permitted for using them in agriculture at the beginning of 1984. The Department of agriculture in Russian Federation considered the problem of using humic chemicals and made a decision to use them on the fields of our country, because the lignitic materials can restore the fertility of our fields. The lignitic materials increase the amount of spore-forming bacteria, mold fungi and actinomycete. Therefore the organic decomposition occurs more strongly, the processes of humification increase the speed and the amount of humus rises in the soil. The new forming humus has a high biological activity and it improves chemical and physical soil properties. The addition of lignitic materials in soil activates different groups of microorganisms, which influence on mobilization of nutrients and transformation from potential to effective fertility. The inclusion of humic fertilizers improves physical, physicochemical properties of soils, its air, water and thermal rate. Humic acids with mineral and organomineral particles of soil form the soil absorbent complex. The inclusion of humic fertilizers promotes the process when humic substances form a very valuable water-stable clumpy-granular structure, which improves water-carrying and water-holding capacity, its air permeability by agglutination of mineral particles with each other. The soils, where humic fertilizers are carried in soils regularly, are more stable for influence of chemical polluting substances (for example, radioactive nuclides, heavy metals, pesticides) than poor soils. The inclusion of humic fertilizers is very important in period of urbanization and cropping on the plough-lands not far from a big industrial area. The lignitic materials tie together the detrimental compounds formed the insoluble complex in soil solution. The detrimental compounds don't go into plants, subsoil waters and atmosphere. The lignitic watering of soils (in concentration from 0.1 to 0.01%) increases biological activity of soil in a man-caused zones and it promotes to stability of plants to detrimental emission of enterprises. Today the problem of processing of sugar-beet industry is very important. In the result of storing sugar-beet wastes the pollution of environment is occurred, examples of this pollution are gassing, salinization of soils and ground waters by filtrational sediments. One of these wastes is defecation sludge. The defecation sludge consists of CaCO3, organic matter, nitrogen, phosphorus, potassium and microelements. The technology of receiving N-Ca fertilizer based on defecate was developed because of impossibility of using this waste in pure form. For available data, using of these fertilizers improves the soil fertility and degree of pollution by heavy metals don't exceed an acceptance limits.

Effect of biogas generation on radon emissions from landfills receiving radium-bearing waste from shale gas development.

PubMed

Walter, Gary R; Benke, Roland R; Pickett, David A

2012-09-01

Dramatic increases in the development of oil and natural gas from shale formations will result in large quantities of drill cuttings, flowback water, and produced water. These organic-rich shale gas formations often contain elevated concentrations of naturally occurring radioactive materials (NORM), such as uranium, thorium, and radium. Production of oil and gas from these formations will also lead to the development of technologically enhanced NORM (TENORM) in production equipment. Disposal of these potentially radium-bearing materials in municipal solid waste (MSW) landfills could release radon to the atmosphere. Risk analyses of disposal of radium-bearing TENORM in MSW landfills sponsored by the Department of Energy did not consider the effect of landfill gas (LFG) generation or LFG control systems on radon emissions. Simulation of radon emissions from landfills with LFG generation indicates that LFG generation can significantly increase radon emissions relative to emissions without LFG generation, where the radon emissions are largely controlled by vapor-phase diffusion. Although the operation of LFG control systems at landfills with radon source materials can result in point-source atmospheric radon plumes, the LFG control systems tend to reduce overall radon emissions by reducing advective gas flow through the landfill surface, and increasing the radon residence time in the subsurface, thus allowing more time for radon to decay. In some of the disposal scenarios considered, the radon flux from the landfill and off-site atmospheric activities exceed levels that would be allowed for radon emissions from uranium mill tailings. Increased development of hydrocarbons from organic-rich shale formations has raised public concern that wastes from these activities containing naturally occurring radioactive materials, particularly radium, may be disposed in municipal solid waste landfills and endanger public health by releasing radon to the atmosphere. This paper analyses the processes by which radon may be emitted from a landfill to the atmosphere. The analyses indicate that landfill gas generation can significantly increase radon emissions, but that the actual level of radon emissions depend on the place of the waste, construction of the landfill cover, and nature of the landfill gas control system.

Geology and uranium deposits of the Cochetopa and Marshall Pass districts, Saguache and Gunnison counties, Colorado

USGS Publications Warehouse

Olson, Jerry C.

1988-01-01

The Cochetopa and Marshall Pass uranium districts are in Saguache and Gunnison Counties, south-central Colorado. Geologic mapping of both districts has shown that their structural history and geologic relationships have a bearing on the distribution and origin of their uranium deposits. In both districts, the principal uranium deposits are situated at the intersection of major faults with Tertiary erosion surfaces. These surfaces were buried by early Tertiary siliceous tuffs-- a likely source of the uranium. That uranium deposits are related to such unconformities in various parts of the world has been suggested by many other authors. The purpose of this study is to understand the geology of the two districts and to define a genetic model for uranium deposits that may be useful in the discovery and evaluation of uranium deposits in these and other similar geologic settings. The Cochetopa and Marshall Pass uranium districts produced nearly 1,200 metric tons of uranium oxide from 1956 to 1963. Several workings at the Los Ochos mine in the Cochetopa district, and the Pitch mine in the Marshall Pass district, accounted for about 97 percent of this production, but numerous other occurrences of uranium are known in the two districts. As a result of exploration of the Pitch deposit in the 1970's, a large open-pit mining operation began in 1978. Proterozoic rocks in both districts comprise metavolcanic, metasedimentary, and igneous units. Granitic rocks, predominantly quartz monzonitic in composition, occupy large areas. In the northwestern part of the Cochetopa district, metavolcanic and related metasedimentary rocks are of low grade (lower amphibolite facies). In the Marshall Pass district, layered metamorphic rocks are predominantly metasedimentary and are of higher (sillimanite subfacies) grade than the Cochetopa rocks. Paleozoic sedimentary rocks in the Marshall Pass district range from Late Cambrian to Pennsylvanian in age and are 700 m thick. The Paleozoic rocks include, from oldest to youngest, the Sawatch Quartzite, Manitou Dolomite, Harding Quartzite, Fremont Dolomite, Parting Formation and Dyer Dolomite of the Chaffee Group, Leadville Dolomite, and Belden Formation. In the Cochetopa district, Paleozoic rocks are absent. Mesozoic sedimentary rocks overlie the Precambrian rocks in the Cochetopa district and comprise the Junction Creek Sandstone, Morrison Formation, Dakota Sandstone, and Mancos Shale. In the Marshall Pass district, Mesozoic rocks are absent and were presumably removed by pre-Tertiary erosion. Tertiary volcanic rocks were deposited on an irregular surface of unconformity; they blanketed both districts but have been eroded, away from much of the area. They include silicic ash flows as well as andesitic lava flows and breccias. In the Marshall Pass district, a 20to 20D-m thickness of waterlaid tuff of early Tertiary age indicates the former presence of a lake over much of the district. In the Cochetopa district, faults have a predominantly east-west trend, and the major Los Ochos fault shows displacement during Laramide time. In the Marshall Pass district, the Chester fault is a major north-trending reverse fault along which Proterozoic rocks have been thrust westward over Paleozoic and Proterozoic rocks. Displacement on the Chester fault was almost entirely of Laramide age. Both faults and old erosion surfaces or unconformities are important in the origin of uranium deposits because of their influence on the movement and localization of ore-forming solutions. In the Cochetopa district, all the known uranium occurrences crop out within 100 m of the inferred position of the unconformity surface beneath the Tertiary volcanic rocks. Much of the district was part of the drainage of an ancestral Cochetopa Creek. The principal uranium deposit, at the Los Ochos mine, is localized along the Los Ochos fault and is near the bottom of the paleovalley where the paleovalley crosses the fault. This

Preliminary Report on the White Canyon Area, San Juan County, Utah

USGS Publications Warehouse

Benson, William Edward Barnes; Trites, A.F.; Beroni, E.P.; Feeger, J.A.

1952-01-01

The White Canyon area in San Juan County, Utah, contains known deposits of copper-uranium ore and is currently being mapped and studied by the Geological Survey. To date, approximately 75 square miles, or about 20 percent of the area, has been mapped on a scale 1 inch=1 mile. The White Canyon area is underlain by more than 2,000 feet of sedimentary rocks, Carboniferous to Jurassic(?) in age. The area is on the flank of the Elk Ridge anticline, and the strata have a regional dip of 1 deg to 2 deg SW. The Shinarump conglomerate of Late Triassic age is the principal ore-bearing formation. The Shinarump consists of lenticular beds of sandstone, conglomeratic sandstone, clay, and siltstone, and ranges in thickness from a feather edge to as much as 75 feet. Locally the sandstones contain silicified and carbonized wood and fragments of charcoal. These vegetal remains are especially common in channel-fill deposits. Jointing is prominent in the western part of the area, and apparently affects all formations. Adjacent to the joints some of the redbeds in the sequence are bleached. Deposits of copper-uranium minerals have been found in the Moenkopi, Shinarump, and Chinle formations, but the only production of ore has been from the Shinarump conglomerate. The largest concentration of these minerals is in the lower third of the Shinarump, and the deposits seem to be controlled in part by ancient channel fills and in part by fractures. Locally precipitation of the copper and uranium minerals apparently has been aided by charcoal and clays. Visible uranium minerals include both hard and soft pitchblende and secondary hydrosulfates, phosphates, and silicates. In addition, unidentified uranium compounds are present in carbonized wood and charcoal, and in veinlets of hydrocarbons. Base-metal sulfides have been identified in all prospects that extend beyond the oxidized zone. Secondary copper minerals in the oxidized zone include the hydrous sulfates and carbonates, and possibly chrysocolla. The principal gangue minerals are quartz, clay minerals, chlorite, oxides of iron and manganese, alunite, calcite, gypsum, pyrite, allophane, gibbsite, opal, and chalcedony. The origin of the copper-uranium ores has not been determined, but the association of many deposits with fractures, the mineralogic assemblage, and a lead-uranium age determination of 50 to 60 million years for the pitchblende in the Happy Jack mine favor the hypothesis that the ores are of hydrothermal origin and were deposited in early Tertiary time. Criteria believed to be the most useful in prospecting for new deposits are (1) visible uranium minerals; (2) visible copper minerals; (3) alunite; (4) hydrocarbons; and (5) bleaching of the underlying Moenkopi formation.

Radioactive source materials in Los Estados Unidos de Venezuela

USGS Publications Warehouse

Wyant, Donald G.; Sharp, William N.; Rodriguez, Carlos Ponte

1953-01-01

This report summarizes the data available on radioactive source materials in Los Estados Unidos de Venezuela accumulated by geologists of the Direccions Tecnica de Geolgia and antecedent agencies prior to June 1951, and the writers from June to November 1951. The investigation comprised preliminary study, field examination, office studies, and the preparation of this report, in which the areas and localities examined are described in detail, the uranium potentialities of Venezuela are summarized, and recommendations are made. Preliminary study was made to select areas and rock types that were known or reported to be radioactive or that geologic experience suggests would be favorable host for uranium deposits, In the office, a study of gamma-ray well logs was started as one means of amassing general radiometric data and of rapidly scanning many of ye rocks in northern Venezuela; gamma-ray logs from about 140 representative wells were examined and their peaks of gamma intensity evaluated; in addition samples were analyzed radiometrically, and petrographically. Radiometic reconnaissance was made in the field during about 3 months of 1951, or about 12 areas, including over 100 localities in the State of Miranda, Carabobo, Yaracuy, Falcon, Lara, Trujillo, Zulia, Merida, Tachira, Bolivar, and Territory Delta Amacuro. During the course of the investigation, both in the filed and office, information was given about geology of uranium deposits, and in techniques used in prospecting and analysis. All studies and this report are designed to supplement and to strengthen the Direccion Tecnica de Geologias's program of investigation of radioactive source in Venezuela now in progress. The uranium potentialities of Los Estados de Venezuela are excellent for large, low-grade deposits of uraniferous phospahtic shales containing from 0.002 to 0.027 percent uranium; fair, for small or moderate-sized, low-grade placer deposits of thorium, rare-earth, and uranium minerals; poor, for high-grade hydrothermal pitchblende deposits; and highly possible for small, medium- to high-grade despots of carnotite-or copper-uranium bearing sandstone. Recommendations for the Venezuelan uranium program include 1) the systematic collection of a mass general radiometric data by examining sample collections, expanding the gamma-ray program, encouraging the use of Geiger counter by field geologists, and by enlisting the aid of the general public; 2) , the examination of specific areas or localities, chosen on the basis of geologic favorability from the results of the amassing of data, or obtained by hints and rumors; 3), the organization of a unit within the Direccion Tecnica de Geologica to direct, collection, and collate metric data. It is emphasized that to be most fruitful the program requires the application of sounds and imaginative geologic theory.

Migration behavior of naturally occurring radionuclides at the Nopal I uranium deposit, Chihuahua, Mexico

NASA Astrophysics Data System (ADS)

Prikryl, James D.; Pickett, David A.; Murphy, William M.; Pearcy, English C.

1997-04-01

Oxidation of pyrite at the Nopal I uranium deposit, Peña Blanca district, Chihuahua, Mexico has resulted in the formation of Fe-oxides/hydroxides. Anomalous U concentrations (i.e. several hundred to several thousand ppm) measured in goethite, hematite, and amorphous Fe-oxyhydroxides in a major fracture that crosscuts the deposit and the absence of U minerals in the fracture suggest that U was retained during secondary mineral growth or sorbed on mineral surfaces. Mobilization and transport of U away from the deposit is suggested by decreasing U concentrations in fracture-infilling materials and in goethite and hematite with distance from the deposit. Greater than unity {234U}/{238U} activity ratios measured in fracture-infilling materials indicate relatively recent ( < 1 Ma) U uptake from fluids that carried excess 234U. Systematic decreases in {234U}/{238U} activity ratios of fracture materials with distance from the deposit suggest a multistage mobilization process, such as remobilization of U from 234U-enriched infill minerals or differential or diminished transport of U-bearing solutions containing excess 234U.

Summary of ground-water quality impacts of uranium mining and milling in the Grants mineral belt, New Mexico. Technical note (final)

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

Kaufmann, R.F.; Eadie, G.G.; Russell, C.R.

Ground-water contamination from uranium mining and milling results from the infiltration of radium-bearing mine, mill, and ion-exchange plant effluents. Radium, selenium, and nitrate were of most value as indicators of contamination. In recent years, mining has increased radium in mine effluents from several picocuries/liter (pCi/1) or less, to 100-150 pCi/1. The shallow aquifer in use in the vicinity of one mill was grossly contaminated with selenium, attributable to the mill tailings. Seepage from two other mill tailings ponds averaged 67,400,000 liters/year and, to date, has contributed an estimated 1.1 curies of radium to ground water. At one of these, anmore » injection well was used to dispose of over 3,400,000,000 liters of waste from 1960-1973. The wastes have not been properly monitored and have apparently migrated to more shallow, potable aquifers. No adverse impacts on municipal water quality in Paguate, Bluewater, Grants, Milan, and Gallup were observed. (GRA)« less

Discrimination of unique biological communities in the Mississippi lignite belt

NASA Technical Reports Server (NTRS)

Miller, W. F. (Principal Investigator); Cutler, J. D.

1981-01-01

Small scale hardcopy LANDSAT prints were manually interpreted and color infrared aerial photography was obtained in an effort to identify and map large contiguous areas of old growth hardwood stands within Mississippi's lignite belt which do not exhibit signs of recent disturbance by agriculture, grazing, timber harvesting, fire, or any natural catastrophe, and which may, therefore, contain unique or historical ecological habitat types. An information system using land cover classes derived from digital LANDSAT data and containing information on geology, hydrology, soils, and cultural activities was developed. Using computer-assisted land cover classifications, all hardwood remnants in the study area which are subject to possible disturbance from surface mining were determined. Twelve rare plants were also identified by botanists.

Comparison of coal reactivityduring conversion into different oxidizing medium

NASA Astrophysics Data System (ADS)

Korotkikh, A. G.; Slyusarskiy, K. V.; Larionov, K. B.; Osipov, V. I.

2016-10-01

Acoal conversion process of different coal samples into three different types of oxidizing medium (argon, air and steam) were studied by means of thermogravimetry. Two coal types with different metamorphism degree (lignite and bituminous coal) were used. The experimental procedure was carried out in non-isothermal conditions in temperature range from 373 K to 1273 K with 20 K/min heating rate. Purge gas consisted of argon and oxidizer with volumetric ratio 1:24 and had 250 ml/min flow rate.The ignition and burnout indexes were calculated to evaluate sample reactivity at different oxidizing mediums. The highest reactivity coefficient values in same atmosphere were obtained for lignite. It was caused by higher particle special surface area and volatile matter content.

Analysis of renewable energy sources and electric vehicle penetration into energy systems predominantly based on lignite

NASA Astrophysics Data System (ADS)

Dedinec, A.; Jovanovski, B.; Gajduk, A.; Markovska, N.; Kocarev, L.

2016-05-01

We consider an integration of renewable energy into transport and electricity sectors through vehicle to grid (V2G) technologies for an energy system that is predominantly based on lignite. The national energy system of Macedonia is modeled using EnergyPLAN which integrates energy for electricity, transport and heat, and includes hourly fluctuations in human needs and the environment. We show that electric-vehicles can provide the necessary storage enabling a fully renewable energy profile for Macedonia that can match the country's growing demand for energy. Furthermore, a large penetration of electric vehicles leads to a dramatic reduction of 47% of small particles and other air pollutants generated by car traffic in 2050.

Ground fissures in the area of Mavropigi Village (N. Greece): Seismotectonics or mining activity?

NASA Astrophysics Data System (ADS)

Kalogirou, Eleni; Tsapanos, Theodoros; Karakostas, Vassilios; Marinos, Vassilios; Chatzipetros, Alexandros

2014-12-01

In the beginning of July 2010, a ground fissure was observed in the field near the village of Mavropigi (Northern Greece) and specifically in its NW side. Later on (early September), a second ground fissure was perceived, close and almost parallel to the first one and very close to the limits of the lignite exploitation mine (by the Public Power Corporation, PPC). It was observed that the village of Mavropigi slides away slowly towards the PPC lignite mine. Geological, seismological, as well as geotechnical survey in the field indicated that the phenomenon is related to the coal mining exploitation in the near vicinity of the village rather than to any seismotectonic activity in the surrounding area.

Validation of gamma-ray detection techniques for safeguards monitoring at natural uranium conversion facilities

NASA Astrophysics Data System (ADS)

Dewji, S. A.; Lee, D. L.; Croft, S.; Hertel, N. E.; Chapman, J. A.; McElroy, R. D.; Cleveland, S.

2016-07-01

Recent IAEA circulars and policy papers have sought to implement safeguards when any purified aqueous uranium solution or uranium oxides suitable for isotopic enrichment or fuel fabrication exists. Under the revised policy, IAEA Policy Paper 18, the starting point for nuclear material under safeguards was reinterpreted, suggesting that purified uranium compounds should be subject to safeguards procedures no later than the first point in the conversion process. In response to this technical need, a combination of simulation models and experimental measurements were employed to develop and validate concepts of nondestructive assay monitoring systems in a natural uranium conversion plant (NUCP). In particular, uranyl nitrate (UO2(NO3)2) solution exiting solvent extraction was identified as a key measurement point (KMP), where gamma-ray spectroscopy was selected as the process monitoring tool. The Uranyl Nitrate Calibration Loop Equipment (UNCLE) facility at Oak Ridge National Laboratory was employed to simulate the full-scale operating conditions of a purified uranium-bearing aqueous stream exiting the solvent extraction process in an NUCP. Nondestructive assay techniques using gamma-ray spectroscopy were evaluated to determine their viability as a technical means for drawing safeguards conclusions at NUCPs, and if the IAEA detection requirements of 1 significant quantity (SQ) can be met in a timely way. This work investigated gamma-ray signatures of uranyl nitrate circulating in the UNCLE facility and evaluated various gamma-ray detector sensitivities to uranyl nitrate. These detector validation activities include assessing detector responses to the uranyl nitrate gamma-ray signatures for spectrometers based on sodium iodide, lanthanum bromide, and high-purity germanium detectors. The results of measurements under static and dynamic operating conditions at concentrations ranging from 10-90 g U/L of natural uranyl nitrate are presented. A range of gamma-ray lines is examined, including attenuation for transmission measurement of density and concentration. It was determined that transmission-corrected gamma-ray spectra provide a reliable way to monitor the 235U concentration of uranyl nitrate solution in transfer pipes in NUCPs. Furthermore, existing predictive and analysis methods are adequate to design and realize practical designs. The 137Cs transmission source employed in this work is viable but not optimal for 235U densitometry determination. Validated simulations assessed the viability of 133Ba and 57Co as alternative densitometry sources. All three gamma-ray detectors are viable for monitoring natural uranium feed; although high-purity germanium is easiest to interpret, it is, however, the least attractive as an installation instrument. Overall, for monitoring throughput in a facility such as UNCLE, emulating the uranium concentration and pump speeds of the Springfields conversion facility in the United Kingdom, an uncertainty of less than 0.17% is required in order to detect the diversion of 1 SQ of uranyl nitrate through changes in uranium concentration over an accountancy period of one year with a detection probability of 50%. Although calibrated gamma-ray detection systems are capable of determining the concentration of uranium content in NUCPs, it is only in combination with verifiable operator declarations and supporting data, such as flow rate and enrichment, that safeguards conclusions can be drawn.

Predicting equilibrium uranium isotope fractionation in crystals and solution

NASA Astrophysics Data System (ADS)

Schauble, E. A.

2015-12-01

Despite the rapidly growing interest in using 238U/235U measurements as a proxy for changes in oxygen abundance in surface and near-surface environments, the present theoretical understanding of uranium isotope fractionation is limited to a few simple gas-phase molecules and analogues of dissolved species (e.g., 1,2,3). Understanding uranium isotope fractionation behavior in more complicated species, such as crystals and adsorption complexes, will help in the design and interpretation of experiments and field studies, and may suggest other uses for 38U/235U measurements. In this study, a recently developed first-principles method for estimating the nuclear volume component of field shift fractionation in crystals and complex molecular species (4) is combined with mass-dependent fractionation theory to predict equilibrium 38U/235U fractionations in aqueous and crystalline uranium compounds, including uraninite (UO2). The nuclear field shift effect, caused by the interaction of electrons with the finite volume of the positive charge distribution in uranium nuclei, is estimated using Density Functional Theory and the Projector Augmented Wave method (DFT-PAW). Tests against relativistic electronic structure calculations and Mössbauer isomer shift data indicate that the DFT-PAW method is reasonably accurate, while being much better suited to models of complex and crystalline species. Initial results confirm previous predictions that the nuclear volume effect overwhelms mass depdendent fractionation in U(VI)-U(IV) exchange reactions, leading to higher 238U/235U in U(IV) species (i.e., for UO2 xtal vs. UO22+aq, ln αNV ≈ +1.8‰ , ln αMD ≈ -0.8‰, ln αTotal ≈ +1.0‰ at 25ºC). UO2 and U(H2O)94+, are within ~0.4‰ of each other, while U(VI) species appear to be more variable. This suggests that speciation is likely to significantly affect natural uranium isotope fractionations, in addition to oxidation state. Tentatively, it appears that uranyl-type (UO22+-bearing) structures will tend to have higher 238U/235U than uranate-type structures that lack strong U=O bonds. References: 1. Bigeleisen (1996) JACS 118:3676; 2. Schauble (2006) Eos 87:V21B-0570; 3. Abe et al. (2008) J Chem Phys 128:144309, 129:164309, & Abe et al. (2010) J Chem Phys 133:044309; 4. Schauble (2013) PNAS 110:17714.

The uranium-bearing nickel-cobalt-native silver deposits in the Black Hawk district, Grant County, New Mexico

USGS Publications Warehouse

Gillerman, Elliot; Whitebread, Donald H.

1953-01-01

The Black Hawk (Bullard Peak) district, Grant County, N. Mex., is 21 miles by road west of Silver City. From 1881 to 1893 more than $1,000,000.00 of high-grade silver ore is reported to have been shipped from the district. Since 1893 there has been no mining in the district except during a short period in 1917 when the Black Hawk mine was rehabilitated. Pre-Cambrian quartz diorite gneiss, which contains inclusions of quartzite, schist, monzonite, and quartz monzonite, is the most widespread rock in the district. The quartz diorite gneiss is intruded by many pre-Cambrian and younger rocks, including diorite granite, diabase, monzonite porphyry and andesite and is overlain by the Upper Cretaceous Beartooth quartzite. The monzonite porphyry, probably of late Cretaceous or early Tertiary age, forms a small stock along the northwestern edge of the district and numerous dikes and irregular masses throughout the district. The ore deposits are in fissure veins that contain silver, cobalt, and uranium. The ore minerals, which include native silver, niccolite, millerite, skutterudite, nickel skutterudite, bismuthinite, pitchblende, and sphalerite, are in a carbonate gangue in narrow, persistent veins, most of which trend northeasterly. Pitchblende has been identified in the Black Hawk and the Alhabra deposits and unidentified radioactive minerals were found at five other localities. The deposits that contain the radioactive minerals constitude a belt 600 to 1,500 feet wide that trends about N. 45° E., and is approximately parallel to the southeastern boundary of the monzonite porphyry stock. All the major ore deposits are in the quartz diorite gneiss in close proximity to the monzonite porphyry. The ore deposits are similar to the deposits at Great Bear Lake, Canada, and Joachimstahl, Czechoslovakia.

ASTER, ALI and Hyperion sensors data for lithological mapping and ore minerals exploration.

PubMed

Beiranvand Pour, Amin; Hashim, Mazlan

2014-01-01

This paper provides a review of the Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER), Advanced Land Imager (ALI), and Hyperion data and applications of the data as a tool for ore minerals exploration, lithological and structural mapping. Spectral information extraction from ASTER, ALI, and Hyperion data has great ability to assist geologists in all disciplines to map the distribution and detect the rock units exposed at the earth's surface. The near coincidence of Earth Observing System (EOS)/Terra and Earth Observing One (EO-1) platforms allows acquiring ASTER, ALI, and Hyperion imagery of the same ground areas, resulting accurate information for geological mapping applications especially in the reconnaissance stages of hydrothermal copper and gold exploration, chromite, magnetite, massive sulfide and uranium ore deposits, mineral components of soils and structural interpretation at both regional and district scales. Shortwave length infrared and thermal infrared bands of ASTER have sufficient spectral resolution to map fundamental absorptions of hydroxyl mineral groups and silica and carbonate minerals for regional mapping purposes. Ferric-iron bearing minerals can be discriminated using six unique wavelength bands of ALI spanning the visible and near infrared. Hyperion visible and near infrared bands (0.4 to 1.0 μm) and shortwave infrared bands (0.9 to 2.5 μm) allowed to produce image maps of iron oxide minerals, hydroxyl-bearing minerals, sulfates and carbonates in association with hydrothermal alteration assemblages, respectively. The techniques and achievements reviewed in the present paper can further introduce the efficacy of ASTER, ALI, and Hyperion data for future mineral and lithological mapping and exploration of the porphyry copper, epithermal gold, chromite, magnetite, massive sulfide and uranium ore deposits especially in arid and semi-arid territory.

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

NONE

In the Bear Creek Valley Watershed Remedial Investigation, the Boneyard/Burnyard was identified as the source of the largest releases of uranium into groundwater and surface water in Bear Creek Valley. The proposed action for remediation of this site is selective excavation and removal of source material and capping of the remainder of the site. The schedule for this action has been accelerated so that this is the first remedial action planned to be implemented in the Bear Creek Valley Record of Decision. Additional data needs to support design of the remedial action were identified at a data quality objectives meetingmore » held for this project. Sampling at the Boneyard/Burnyard will be conducted through the use of a phased approach. Initial or primary samples will be used to make in-the-field decisions about where to locate follow-up or secondary samples. On the basis of the results of surface water, soil, and groundwater analysis, up to six test pits will be dug. The test pits will be used to provide detailed descriptions of source materials and bulk samples. This document sets forth the requirements and procedures to protect the personnel involved in this project. This document also contains the health and safety plan, quality assurance project plan, waste management plan, data management plan, implementation plan, and best management practices plan for this project as appendices.« less

Uranium deposits at Shinarump Mesa and some adjacent areas in the Temple Mountain district, Emery County, Utah

USGS Publications Warehouse

Wyant, Donald G.

1953-01-01

Deposits of uraniferous hydrocarbons are associated with carnotite in the Shinarump conglomerate of Triassic age at Shinarump Mesa and adjacent areas of the Temple Mountain district in the San Rafael Swell of Emery County, Utah. The irregular ore bodies of carnotite-bearing sandstone are genetically related to lenticular uraniferous ore bodies containing disseminated asphaltitic and humic hydrocarbon in permeable sandstones and were localized indirectly by sedimentary controls. Nearly non-uraniferous bitumen commonly permeates the sandstones in the Shinarump conglomerate and the underlying Moekopi formation in the area. The ore deposits at Temple Mountain have been altered locally by hydrothermal solutions, and in other deposits throughout the area carnotite has been transported by ground and surface water. Uraniferous asphaltite is thought to be the non-volatile residue of an original weakly uraniferous crude oil that migrated into the San Rafael anticline; the ore metals concentrated in the asphaltite as the oil was devolatilized and polymerized. Carnotite is thought to have formed from the asphaltite by ground water leaching. It is concluded that additional study of the genesis of the asphaltitic uranium ores in the San Rafael Swell, of the processes by which the hydrocarbons interact and are modified (such as heat, polymerization, and hydrogenation under the influence of alpha-ray bombardment), of petroleum source beds, and of volcanic intrusive rocks of Tertiary age are of fundamental importance in the continuing study of the uranium deposits on the Colorado Plateau.

Redox bias in loss of ignition moisture measurement for relatively pure plutonium-bearing oxide materials.

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

Eller, P. G.; Stakebake, J. L.; Cooper, T. D.

2001-01-01

This paper evaluates potential analytical bias in application of the Loss on Ignition (LOI) technique for moisture measurement to relatively pure (plutonium assay of 80 wt.% or higher) oxides containing uranium that have been stabilized according to stabilization and storage standard DOE-STD-3013-2000 (STD-3013). An immediate application is to Rocky Flats (RF) materials derived from highgrade metal hydriding separations subsequently treated by multiple calcination cycles. Specifically evaluated are weight changes due to oxidatiodreduction of multivalent impurity oxides that could mask true moisture equivalent content measurement. Process knowledge and characterization of materials representing complex-wide materials to be stabilized and packaged according tomore » STD-3013, and particularly for the immediate RF target stream, indicate that oxides of uranium, iron and gallium are the only potential multivalent constituents expected to be present above 0.5 wt.%. The evaluation shows that of these constituents, with few exceptions, only uranium oxides can be present at a sufficient level to produce weight gain biases significant with respect to the LO1 stability test. In general, these formerly high-value, high-actinide content materials are reliably identifiable by process knowledge and measurement. Si&icant bias also requires that UO1 components remain largely unoxidized after calcination and are largely converted to U30s clsning LO1 testing at only slightly higher temperatures. Based on wellestablished literature, it is judged unlikely that this set of conditions will be realized in practice. We conclude that it is very likely that LO1 weight gain bias will be small for the immediate target RF oxide materials containing greater than 80 wt.% plutonium plus a much smaller uranium content. Recommended tests are in progress to confum these expectations and to provide a more authoritative basis for bounding LO1 oxidatiodreduction biases. LO1 bias evaluation is more difficult for lower purity materials and for fuel-type uranium-plutonium oxides. However, even in these cases testing may show that bias effects are manageable.« less

Hydrologic characteristics and possible effects of surface mining in the northwestern part of West Branch Antelope Creek basin, Mercer County, North Dakota

USGS Publications Warehouse

Crawley, Mark E.; Emerson, Douglas G.

1981-01-01

Lignite beds and abundant discontinuous sandstone beds of the Paleocene Sentinel Butte Member of the Fort Union Formation and sand and gravel beds in the Quarternary glaciofluvial deposits (Antelope Creek aquifer) are the most important aquifers for domestic and livestock water supplies in the West Branch Antelope Creek basin. In the Beulah-Zap lignite, ground water moves from highland area in the west toward the Antelope Creek aquifer. Water levels in the basal Sentinel Butte sandstone appear to be controlled by the level of Lake Sakakawea. In the glaciofluvial deposits of the Antelope Creek aquifer water moves from a ground-water divide northwestward to Lake Sakakawea and southeastward toward the Knife River. Large water-level declines in wells completed in the lignite and shallower aquifers could be expected with mining. The effects probably would be limited to within 1 to 2 miles of an active mine. Surface-runoff duration could be altered by increased infiltration and retention in the reclaimed are and possible temporal extension of base flow could occur. Shallow ground water beneath mine sites would be expected to increase in dissolved solids and locally to contain large sodium and sulfate concentrations. In some locations movement of poor quality water toward the Antelope Creek aquifer would be expected. (USGS)

Preparation and Evaluation of Adsorbents from Coal and Irvingia gabonensis Seed Shell

NASA Astrophysics Data System (ADS)

Ezeokonkwo, Mercy A.; Ofor, Okechukwu F.; Ani, Julius U.

2017-12-01

The adsorption of Cd(II) and Pb(II) ions on adsorbents prepared from sub-bituminous coal, lignite and a blend of coal and Irvingia gabonensis seed shells was investigated. Fourier transform infrared, scanning electron microscope and X-ray fluorescence analyses implicated hydroxyl, carbonyl, Al2O3 and SiO2 as being responsible for binding the metal ions on the porous adsorbents. The optimum adsorption of carbonized lignite for the removal of Cd(II) and Pb(II) ions from aqueous media were 80.93% and 87.85%, respectively. Batch adsorption was done by effect of adsorbent dosage, pH, contact time, temperature, particle size, and initial concentration. Equilibrium for the removal of Pb(II) and Cd(II) was established within 100 and 120 min respectively. Blending the lignite-derived adsorbent with Irvingia gabonensis seed shell improved the performance significantly. More improvement was observed on modification of the blend using NaOH and H3PO4. Pb(II) was preferentially adsorbed than Cd(II) in all cases. Adsorption of Cd(II) and Pb(II) ions followed Langmuir isotherm. The kinetics of adsorption was best described by pseudo-second order model. The potential for using a blend of coal and agricultural byproduct (Irvingia gabonensis seed shell) was found to be a viable alternative for removal of toxic heavy metals from aqueous solutions.

Simulation of 0.3 MWt AFBC test rig burning Turkish lignites

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

Selcuk, N.; Degirmenci, E.; Oymak, O.

1997-12-31

A system model coupling bed and freeboard models for continuous combustion of lignite particles of wide size distribution burning in their own ash in a fluidized bed combustor was modified to incorporate: (1) a procedure for faster computation of particle size distributions (PSDs) without any sacrifice in accuracy; (2) energy balance on char particles for the determination of variation of temperature with particle size, (3) plug flow assumption for the interstitial gas. An efficient and accurate computer code developed for the solution of the conservation equations for energy and chemical species was applied to the prediction of the behavior ofmore » a 0.3 MWt AFBC test rig burning low quality Turkish lignites. The construction and operation of the test rig was carried out within the scope of a cooperation agreement between Middle East Technical University (METU) and Babcock and Wilcox GAMA (BWG) under the auspices of Canadian International Development Agency (CIDA). Predicted concentration and temperature profiles and particle size distributions of solid streams were compared with measured data and found to be in reasonable agreement. The computer code replaces the conventional numerical integration of the analytical solution of population balance with direct integration in ODE form by using a powerful integrator LSODE (Livermore Solver for Ordinary Differential Equations) resulting in two orders of magnitude decrease in CPU (Central Processing Unit) time.« less

The solubilization of low-ranked coals by microorganisms

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

Strandberg, G.W.

1987-07-09

Late in 1984, our Laboratory was funded by the Pittsburgh Energy Technology Center, US Department of Energy, to investigate the potential utility of microorganisms for the solubilization of low-ranked coals. Our approach has been multifacited, including studies of the types of microorganisms involved, appropriate conditions for their growth and coal-solubilization, the suceptibility of different coals to microbial action, the chemical and physical nature of the product, and potential bioprocess designs. A substantial number of fungal species have been shown to be able to solubilize coal. Cohen and Gabrielle reported that two lignin-degrading fungi, Polyporous (Trametes) versicolor and Poria monticola couldmore » solubilize lignite. Ward has isolated several diverse fungi from nature which are capable of degrading different lignites, and our Laboratory has isolated three coal-solubilizing fungi which were found growing on a sample of Texas lignite. The organisms we studied are shown in Table 1. The perceived significance of lignin degradation led us to examine two lignin-degrading strains of the genus Streptomyces. As discussed later, these bacteria were capable of solubilizing coal; but, in the case of at least one, the mechanism was non-enzymatic. The coal-solubilizing ability of other strains of Streptomyces was recently reported. Fakoussa and Trueper found evidence that a strain of Pseudomonas was capble of solubizing coal. It would thus appear that a diverse array of microorganisms possess the ability to solubilize coal. 16 refs.« less

Isolation and identification of a Candida digboiensis strain from an extreme acid mine drainage of the Lignite Mine, Gujarat.

PubMed

Patel, Mitesh J; Tipre, Devayani R; Dave, Shailesh R

2009-12-01

An extremely acidic mine drainage (AMD) water sample was collected in 1998 and 2008 from Panandhro lignite mine, Gujarat, India. The yeast isolated from this sample was identified using mini API identification system, as a member of genus Candida. The major cellular fatty acids detected by FAME from the isolate are C(16:0) and C(18:2) (cis 9,12)/C(18:0alpha) as 25.23 and 19.5%, respectively. The isolate was identified as Candida digboiensis by 18S rRNA gene sequence analysis and designated as Candida digboiensis SRDyeast1. Phylogenetic analysis using D1/D2 variable domains showed that the closest relative of this strain is Candida blankii with 3% divergence. This organism has been reported for the first time from the lignite mine AMD sample, and for cellular fatty acid analysis. This yeast is able to survive in the AMD sample preserved at 10-42 degrees C temperature since last 10 years along with iron oxidizing microorganisms. It can grow in the presence of 40% glucose, 10% NaCl and in the pH range of 1 to 10. The isolate is capable of producing enzymes like protease and lipase. This isolate differs from the type strain Candida digboiensis in as many as six physiological and metabolic characteristics.

Chemical investigations of aquifers affected by pyrite oxidation in the Bitterfeld lignite district.

PubMed

Grützmacher, G; Hindel, R; Kantor, W; Wimmer, R

2001-01-01

In a large area around the former open-pit lignite mines near Bitterfeld, Germany, groundwater taken from wells was analyzed for the major cations, anions, and trace elements. Quaternary and Tertiary sediments were collected from aquifers exposed on the sides of the pits and from boreholes outside the mines and analyzed for major and trace elements, as well as for carbonate, pyritic sulfur and total organic carbon. The pH and electrical conductivity of the sediments in suspension were measured. Significant differences were determined between the Tertiary sediments of the aquifers that were exposed to atmospheric oxygen during the lowering of the groundwater table and those outside the cone of depression. The greatest differences were found in the pyrite content, the pH values, and the electrical conductivity. In order to map the degree to which the mining of the lignite has affected the quality of the groundwater in the study area, the water samples were divided into six classes on the basis of their sulfate content. The neutralization potential was calculated to estimate the potential for acidification. Prediction of future groundwater quality is based on both (i) the present composition of the groundwater, surface water, and Quaternary and Tertiary aquifer sediments and (ii) the present and future groundwater flow directions. These studies have shown which parameters are important for future groundwater monitoring.

Valorization of lignite combustion residues and ferroalumina in the production of aggregates.

PubMed

Anagnostopoulos, I M; Stivanakis, V E; Angelopoulos, G N; Papamantellos, D C

2010-02-15

The present research study investigates the synergy of industrial solid by-products from lignite combustion (fly ash and bottom ash) and aluminum production (ferroalumina) in the production of lightweight aggregates (LWA). The process consists of two stages, pelletization and sintering. Bottom ash (BA) is used as the principal raw material in mixtures while ferroalumina (FAL) is added in lower percentages (5-30 wt%). BA carbon content is used as the fuel of sintering process in high temperatures, around 1250 degrees C, and gas generation is responsible for porous structure formation. Physical properties such as porosity, water absorption and bulk density, of sintering products are measured. Increase of FAL percentage in sintering mixtures results in decrease of porosity from 61% to 35% and of water absorption from 61% to 21% and in increase of bulk density from 1.02 g/cm(3) to 1.80 g/cm(3) of the produced aggregates. Aggregates produced by FAL addition up to 20 wt% are characterized as LWA. Aggregates formed are used in the production of concrete specimens. Compressive strength of concrete increases by increasing FAL addition in aggregates from 5 wt% to 15 wt% (highest strength value), while decrease by increasing FAL addition from 20 wt% to 30 wt%. FAL addition in lignite ashes sintering mixtures (up to 15 wt%) is considered as an important parameter for enhancing aggregates strength.

Direct comparison of XAFS spectroscopy and sequential extraction for arsenic speciation in coal

USGS Publications Warehouse

Huggins, Frank E.; Huffman, G.P.; Kolker, A.; Mroczkowski, S.; Palmer, C.A.; Finkelman, R.B.

2000-01-01

The speciation of arsenic in an Ohio bituminous coal and a North Dakota lignite has been examined by the complementary methods of arsenic XAFS spectroscopy and sequential extraction by aqueous solutions of ammonium acetate, HCl, HF, and HNO3. In order to facilitate a more direct comparison of the two methods, the arsenic XAFS spectra were obtained from aliquots of the coal prepared after each stage of the leaching procedure. For the aliquots, approximately linear correlations (r2 > 0.98 for the Ohio coal, > 0.90 for the ND lignite) were observed between the height of the edge-step in the XAFS analysis and the concentration of arsenic measured by instrumental neutron activation analysis. Results from the leaching sequence indicate that there are two major arsenic forms present in both coals; one is removed by leaching with HCl and the other by HNO3. Whereas the XAFS spectral signatures of the arsenic leached by HCl are compatible with arsenate for both coals, the arsenic leached by HNO3 is identified as arsenic associated with pyrite for the Ohio coal and as an As3+ species for the North Dakota lignite. Minor arsenate forms persist in both coals after the final leaching with nitric acid. The arsenate forms extracted in HCl are believed to be oxidation products derived from the other major arsenic forms upon exposure of the pulverized coals to air.

Optimization of on-line hydrogen stable isotope ratio measurements of halogen- and sulfur-bearing organic compounds using elemental analyzer-chromium/high-temperature conversion isotope ratio mass spectrometry (EA-Cr/HTC-IRMS).

PubMed

Gehre, Matthias; Renpenning, Julian; Geilmann, Heike; Qi, Haiping; Coplen, Tyler B; Kümmel, Steffen; Ivdra, Natalija; Brand, Willi A; Schimmelmann, Arndt

2017-03-30

Accurate hydrogen isotopic analysis of halogen- and sulfur-bearing organics has not been possible with traditional high-temperature conversion (HTC) because the formation of hydrogen-bearing reaction products other than molecular hydrogen (H 2 ) is responsible for non-quantitative H 2 yields and possible hydrogen isotopic fractionation. Our previously introduced, new chromium-based EA-Cr/HTC-IRMS (Elemental Analyzer-Chromium/High-Temperature Conversion Isotope Ratio Mass Spectrometry) technique focused primarily on nitrogen-bearing compounds. Several technical and analytical issues concerning halogen- and sulfur-bearing samples, however, remained unresolved and required further refinement of the reactor systems. The EA-Cr/HTC reactor was substantially modified for the conversion of halogen- and sulfur-bearing samples. The performance of the novel conversion setup for solid and liquid samples was monitored and optimized using a simultaneously operating dual-detection system of IRMS and ion trap MS. The method with several variants in the reactor, including the addition of manganese metal chips, was evaluated in three laboratories using EA-Cr/HTC-IRMS (on-line method) and compared with traditional uranium-reduction-based conversion combined with manual dual-inlet IRMS analysis (off-line method) in one laboratory. The modified EA-Cr/HTC reactor setup showed an overall H 2 -recovery of more than 96% for all halogen- and sulfur-bearing organic compounds. All results were successfully normalized via two-point calibration with VSMOW-SLAP reference waters. Precise and accurate hydrogen isotopic analysis was achieved for a variety of organics containing F-, Cl-, Br-, I-, and S-bearing heteroelements. The robust nature of the on-line EA-Cr/HTC technique was demonstrated by a series of 196 consecutive measurements with a single reactor filling. The optimized EA-Cr/HTC reactor design can be implemented in existing analytical equipment using commercially available material and is universally applicable for both heteroelement-bearing and heteroelement-free organic-compound classes. The sensitivity and simplicity of the on-line EA-Cr/HTC-IRMS technique provide a much needed tool for routine hydrogen-isotope source tracing of organic contaminants in the environment. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

In situ calibration of a high-resolution gamma-ray borehole sonde for assaying uranium-bearing sandstone deposits

USGS Publications Warehouse

Day, J.H.

1985-01-01

A method is presented for assaying radioactive sandstone deposits in situ by using a high-resolution borehole gamma-ray spectrometer. Gamma-ray photopeaks from the same spectrum acquired to analyze a sample are used to characterize gamma-ray attenuation properties, from which a calibration function is determined. Assay results are independent of differences between properties of field samples and those of laboratory or test-hole standards generally used to calibrate a borehole sonde. This assaying technique is also independent of the state of radioactive disequilibrium that usually exists in nature among members of the natural-decay chains. ?? 1985.

Coal desulfurization by low temperature chlorinolysis, phase 1

NASA Technical Reports Server (NTRS)

Kalvinskas, J. J.; Hsu, G. C.; Ernest, J. B.; Andress, D. F.; Feller, D. R.

1977-01-01

The reported activity covers laboratory scale experiments on twelve bituminous, sub-bituminous and lignite coals, and preliminary design and specifications for bench-scale and mini-pilot plant equipment.

30 CFR 75.380 - Escapeways; bituminous and lignite mines.

Code of Federal Regulations, 2010 CFR

2010-07-01

...) Underground transformer stations, battery charging stations, substations, and rectifiers except— (A) Where... rectifiers and power centers with transformers that are either dry-type or contain nonflammable liquid...

Energy production for environmental issues in Turkey

NASA Astrophysics Data System (ADS)

Yuksel, Ibrahim; Arman, Hasan; Halil Demirel, Ibrahim

2017-11-01

Due to the diversification efforts of energy sources, use of natural gas that was newly introduced into Turkish economy, has been growing rapidly. Turkey has large reserves of coal, particularly of lignite. The proven lignite reserves are 8.0 billion tons. The estimated total possible reserves are 30 billion tons. Turkey, with its young population and growing energy demand per person, its fast growing urbanization, and its economic development, has been one of the fast growing power markets of the world for the last two decades. It is expected that the demand for electric energy in Turkey will be 580 billion kWh by the year 2020. Turkey's electric energy demand is growing about 6-8% yearly due to fast economic growing. This paper deals with energy demand and consumption for environmental issues in Turkey.

Wetter and cooler: pronounced temperate climate conditions in western Anatolia during the Middle Miocene Climatic Optimum

NASA Astrophysics Data System (ADS)

Güner, Tuncay H.; Bouchal, Johannes M.; Köse, Nesibe; Denk, Thomas

2017-04-01

During the course of an ongoing palaeobotanical investigation of the lignite mines of the Yataǧan Basin, Muǧla province, Turkey, the fossil leaves of the Eskihisar lignite mine were analysed using the Climate Leaf Analysis Multivariate Program (CLAMP). The investigated fossil leaves derive from the marls and clayey limestones (Sekköy Member) overlying the exploited lignite seam (uppermost Turgut Member). The age of the studied sedimentary rocks is well constrained by vertebrate fossils occuring in the main lignite seam (MN6 → Gomphoterium angustidens Cuvier, 1817; Percrocuta miocenica Pavlov & Thenius, 1965) and at the Yenieskihisar Mammal locality (MN7/8, uppermost Sekköy Member). 719 specimens were measured and assigned to 65 leaf morphotypes. Using this data, CLAMP reconstructed the following climate parameters: mean annual temperature (MAT) 12.58 (+/-1.5)°C, warm month mean temperature (WMMT) 23.72 (+/-2.5)°C, cold month mean temperature (WMMT) 2.29 (+/-2)°C, length of growing season (LGS) 7.52 (+/-0.75) month, mean growing season precipitation (GSP) 130.1 (+/-40) cm, precipitation during the three wettest months (3-WET) 67 (+/-25) cm, precipitation during the three driest months (3-DRY) 20.4 (+/-7.5) cm. The reconstructed parameters are too cool for tropical climates (the 18˚ C winter isotherm being a threshold for tropical climates) and indicate temperate conditions; climates fitting these parameters (Cfb according to the Köppen-Geiger climate classification) can be found today in regions known as "Tertiary relict areas" (e.g. Black sea coast of Northeast Turkey, eastern China, Japan). Based on a substantial amount of rainfall during the three driest months, it is further possible to exclude markedly seasonal climates such as a summer-dry and winter-wet Mediterranean climate and a summer-wet and winter-dry monsoon climate as commonly found along the southern foothills of the Himalayas and in southwestern China. Instead, a fully humid Cf climate is proposed that has only a weak seasonality in precipitation (lower precipitation in winter). The findings of our study provide valuable information for inferring palaeoenvironments of middle Miocene rich ungulate faunas in western Turkey (e.g. Paşalar), for which seasonal tropical and subtropical forest communities have been proposed (Andrews, 1990). The fossil floras of the Tınaz and Salihpaşalar lignite mines, representing the Tınaz sub-basin and the main basin of the wider Yataǧan Basin, are investigated at the moment, and a synthesis paper combining and comparing evidence from the macro floral and palynological data is soon to be submitted. Andrews. (1990) Palaeoecology of the Miocene fauna from Paşalar, Turkey. Journal of Human evolution 19:569-582.

Detailed mineral and chemical relations in two uranium-vanadium ores

USGS Publications Warehouse

Garrels, Robert M.; Larsen, E. S.; Pommer, A.M.; Coleman, R.G.

1956-01-01

Channel samples from two mines on the Colorado Plateau have been studied in detail both mineralogically and chemically. A channel sample from the Mineral Joe No. 1 mine, Montrose County, Colo., extends from unmineralized rock on one side, through a zone of variable mineralization, into only weakly mineralized rock. The unmineralized rock is a fairly clean quartz sand cemented with gypsum and contains only minor amounts of clay minerals. One boundary between unmineralized and mineralized rock is quite sharo and is nearly at right angles to the bedding. Vanadium clay minerals, chiefly mixed layered mica-montmorillonite and chlorite-monmorillonite, are abundant throughout the mineralized zone. Except in the dark "eye" of the channel sample, the vanadium clay minerals are accompanied by hewettite, carnotite, tyuyamunite, and probably unidentified vanadates. In the dark "eye," paramontroseite, pyrite, and marcasite are abundant, and bordered on each side by a zone containing abundant corvusite. No recognizable uranium minerals were seen in the paramontroseite zone although uranium is abundant there. Coaly material is recognizable throughout all of the channel but is most abundant in and near the dark "eye." Detailed chemical studies show a general increase in Fe, Al, U, and V, and a decrease in SO4 toward the "eye" of the channel. Reducing capacity studies indicate that V(IV) and Fe(II) are present in the clay mineral throughout the channel, but only in and near the "eye" are other V(IV) minerals present (paramontroseite and corvusite). The uranium is sexivalent, although its state of combination is conjectural where it is associated with paramontroseite. Where the ore boundary is sharp, the boundary of introduced trace elements is equally sharp. Textural and chemical relations leave no doubt that the "eye: is a partially oxidized remnant of a former lower-valence ore, and the remainder of the channel is a much more fully oxidized remnant. A channel sample from the Virgin No. 3 mine, Montrose County, Colo., extends from weakly mineralized sandstone on both sides through a strongly mineralized central zone. The weakly mineralized zone is a poorly sorted sandstone with common detrital clay partings; chlorite and mixed layer mica-montmorrillonite are abundant interstitial to the quartz grains. No distinct vanadium or uranium minerals are recognizable, although the clay minerals are vanadium bearing. Euherdral pyrite grains and selenian galena are present but rare. The strongly mineralized rock is separated from the weakly mineralized rock by a narrow transition zone which only apporiximates the bedding planes. It contains abundant vanadium-bearing clay minerals (predominantly chlorite) interstitial to the quartz grains, and apparently replacing them. Paramontroseite is common and is intergrown with the clay minerals. Pyrite and marcasite are present, chiefly in or near the abundant blebs and fragments of carbonaceous material. Selenian galena is rarely present, and generally in or near carbonaceous material. Coffinite is the only uranium mineral idenitified; it is extremely fine grained and was identified only in X-ray diffraction patterns of heavy separates. Distribution of trace elements is not clear; some are consistently high in the strongly mineralized rocks, and some are consistently low. The trace element composition of the unmineralized rock is not known. Chemical studies show a very abrupt rise in the total U, V, and Fe from the weakly mineralized to strongly mineralized rock. Reducing-capacity studies indicate that most of the vanadium is present as V(IV), but some is present as V(V); that iron is present as both Fe(II) and Fe(III), the latter believed to have been present in the primary clays of the unmineralized rock; and that come of the uranium is present as U(VI) in addition to the U(IV) in the coffinite. All evidence points to weak oxidation of an ore once having a somewhat lower valence state. The channel samples from both the Mineral Joe No. 1 mine and the Virgin No. 3 mine are believe to have been essentially identical in mineralogy prior to oxidation by weathering: vanadium was present as V(III) in montroseite and V(IV) in the vanadium clays; uranium was present largely as U(IV) in coffinite and/or uraninite. The Mineral Joe No. 1 mine channel sample is now more fully oxidized. Vanadium clays are unquestionably formed abundantly during the primary mineralization, and they persist with a minimum of alteration during much of the weathering. They suggest that the vanadium is carried as V(IV) in the ore-forming fluids; it seems likely too that the uranium is carried as a U(VI) ion.

A method for the estimation of dual transmissivities from slug tests

NASA Astrophysics Data System (ADS)

Wolny, Filip; Marciniak, Marek; Kaczmarek, Mariusz

2018-03-01

Aquifer homogeneity is usually assumed when interpreting the results of pumping and slug tests, although aquifers are essentially heterogeneous. The aim of this study is to present a method of determining the transmissivities of dual-permeability water-bearing formations based on slug tests such as the pressure-induced permeability test. A bi-exponential rate-of-rise curve is typically observed during many of these tests conducted in heterogeneous formations. The work involved analyzing curves deviating from the exponential rise recorded at the Belchatow Lignite Mine in central Poland, where a significant number of permeability tests have been conducted. In most cases, bi-exponential movement was observed in piezometers with a screen installed in layered sediments, each with a different hydraulic conductivity, or in fissured rock. The possibility to identify the flow properties of these geological formations was analyzed. For each piezometer installed in such formations, a set of two transmissivity values was calculated piecewise based on the interpretation algorithm of the pressure-induced permeability test—one value for the first (steeper) part of the obtained rate-of-rise curve, and a second value for the latter part of the curve. The results of transmissivity estimation for each piezometer are shown. The discussion presents the limitations of the interpretational method and suggests future modeling plans.

Validation of gamma-ray detection techniques for safeguards monitoring at natural uranium conversion facilities

DOE PAGES

Dewji, Shaheen A.; Lee, Denise L.; Croft, Stephen; ...

2016-03-28

Recent IAEA circulars and policy papers have sought to implement safeguards when any purified aqueous uranium solution or uranium oxides suitable for isotopic enrichment or fuel fabrication exists. Under the revised policy, IAEA Policy Paper 18, the starting point for nuclear material under safeguards was reinterpreted, suggesting that purified uranium compounds should be subject to safeguards procedures no later than the first point in the conversion process. In response to this technical need, a combination of simulation models and experimental measurements were employed to develop and validate concepts of nondestructive assay monitoring systems in a natural uranium conversion plant (NUCP).more » In particular, uranyl nitrate (UO 2(NO 3) 2) solution exiting solvent extraction was identified as a key measurement point (KMP), where gamma-ray spectroscopy was selected as the process monitoring tool. The Uranyl Nitrate Calibration Loop Equipment (UNCLE) facility at Oak Ridge National Laboratory was employed to simulate the full-scale operating conditions of a purified uranium-bearing aqueous stream exiting the solvent extraction process in an NUCP. Nondestructive assay techniques using gamma-ray spectroscopy were evaluated to determine their viability as a technical means for drawing safeguards conclusions at NUCPs, and if the IAEA detection requirements of 1 significant quantity (SQ) can be met in a timely way. This work investigated gamma-ray signatures of uranyl nitrate circulating in the UNCLE facility and evaluated various gamma-ray detector sensitivities to uranyl nitrate. These detector validation activities include assessing detector responses to the uranyl nitrate gamma-ray signatures for spectrometers based on sodium iodide, lanthanum bromide, and high-purity germanium detectors. The results of measurements under static and dynamic operating conditions at concentrations ranging from 10–90 g U/L of natural uranyl nitrate are presented. A range of gamma-ray lines is examined, including attenuation for transmission measurement of density and concentration. It was determined that transmission-corrected gamma-ray spectra provide a reliable way to monitor the 235U concentration of uranyl nitrate solution in transfer pipes in NUCPs. Furthermore, existing predictive and analysis methods are adequate to design and realize practical designs. The 137Cs transmission source employed in this work is viable but not optimal for 235U densitometry determination. Validated simulations assessed the viability of 133Ba and 57Co as alternative densitometry sources. All three gamma-ray detectors are viable for monitoring natural uranium feed; although high-purity germanium is easiest to interpret, it is, however, the least attractive as an installation instrument. Overall, for monitoring throughput in a facility such as UNCLE, emulating the uranium concentration and pump speeds of the Springfields conversion facility in the United Kingdom, an uncertainty of less than 0.17% is required in order to detect the diversion of 1 SQ of uranyl nitrate through changes in uranium concentration over an accountancy period of one year with a detection probability of 50%. As a result, calibrated gamma-ray detection systems are capable of determining the concentration of uranium content in NUCPs, it is only in combination with verifiable operator declarations and supporting data, such as flow rate and enrichment, that safeguards conclusions can be drawn.« less

Water resources of the Fort Berthold Indian Reservation, west-central North Dakota

USGS Publications Warehouse

Cates, Steven W.; Macek-Rowland, Kathleen M.

1998-01-01

Water resources of the Fort Berthold Indian Reservation in west-central North Dakota occur as ground water in bedrock and buried-valley aquifers and as surface water in streams and Lake Sakakawea. The bedrock aquifers-the Fox Hills-Hell Creek, Tongue River, and Sentinel Butte store about 93 million acre-feet of water under the Reservation. The Fox Hills-Hell Creek aquifer is composed mainly of very fine to medium-grained sandstone and stores about 51 million acrefeet of water. Water levels in the aquifer declined from 1976 through 1992. The Tongue River aquifer is composed mainly of claystones and siltstones and has widely distributed pockets of sandstone or lignite layers. The aquifer stores about 24 million acre-feet of water. The Sentinel Butte aquifer is composed mainly of interbedded claystones, siltstones, shale, lignite, and sandstone and stores about 18 million acre-feet of water. Yields from the lignite beds are highly variable. Water in the aquifers was predominantly a sodium bicarbonate type. Mean dissolved solids concentrations were 1,530 milligrams per liter in water from the Fox Hills-Hell Creek aquifer, 2,110 milligrams per liter in water from the Tongue River aquifer, and 1,300 milligrams per liter in water from the Sentinel Butte aquifer. The East Fork Shell Creek, Shell Creek, White Shield, New Town, and Sanish aquifers occur within buried valleys and store about 1,414,000 acre-feet of water. The East Fork Shell Creek and Shell Creek aquifers are composed of sand and gravel lenses that are surrounded by less permeable till. Water in the East Fork Shell Creek aquifer is a sodium sulfate bicarbonate type, and water in the Shell Creek aquifer is a sodium bicarbonate sulfate type. Mean dissolved-solids concentrations were 3,220 milligrams per liter in water from the East Fork Shell Creek aquifer and 1,470 milligrams per liter in water from the Shell Creek aquifer.The White Shield aquifer is composed of very fine to coarse sand and fine to coarse gravel. Water in the aquifer varies from a sodium bicarbonate sulfate type to a mixed calcium magnesium sodium bicarbonate sulfate type. Mean dissolved-solids concentrations were 1,080 milligrams per liter in water from the eastern part of the aquifer and 1,430 milligrams per liter in water from the western part of the aquifer. Water levels in the western part of the aquifer rose during 1970-92. The New Town aquifer is composed of lenticular deposits of sand and gravel. Water in the aquifer is a calcium sodium bicarbonate sulfate type and had a mean dissolved-solids concentration of 1,390 milligrams per liter. Data indicate a close correspondence between ground-water levels and lake stage of Lake Sakakawea, implying a hydraulic connection between the aquifer and the lake.The Sanish aquifer is composed of sand, clayey sand, and thin gravels that are poorly cemented and highly permeable. Water in the aquifer is a mixed calcium magnesium bicarbonate sulfate type and had a mean dissolved-solids concentration of 1,350 milligrams per liter.Major streams on the Reservation are Bear Den Creek, Shell Creek, East Fork Shell Creek, Deepwater Creek, Moccasin Creek, and Squaw Creek. Mean streamflow for Bear Den Creek for June 1966 through September 1992 was 6.72 cubic feet per second. Mean streamflow for Shell Creek for September 1965 through September 1981 was 12.9 cubic feet per second. Streamflow measurements for East Fork Shell Creek for April 1990 through June 1991 ranged from zero to 3.65 cubic feet per second, measurements for Deepwater Creek for April 1990 through May 1991 ranged from zero to 4.28 cubic feet per second, measurements for Moccasin Creek for April 1990 through September 1992 ranged from zero to 7.07 cubic feet per second, and measurements for Squaw Creek for April 1990 through September 1992 ranged from zero to 4.22 cubic feet per second. Lake Sakakawea has a maximum surface area of 390,000 acres. The surface area is variable in relation to lake stage, which was unusually low during this study. The mean lake elevation for Lake Sakakawea for 1970-92 was 1,837.08 feet, and the mean lake elevation for 1990-92 was 1,821.14 feet.

Role of NSO compounds during primary cracking of a Type II kerogen and a Type III lignite

USGS Publications Warehouse

Behar, F.; Lorant, F.; Lewan, M.

2008-01-01

The aim of this work is to follow the generation of NSO compounds during the artificial maturation of an immature Type II kerogen and a Type III lignite in order to determine the different sources of the petroleum potential during primary cracking. Experiments were carried out in closed system pyrolysis in the temperature range from 225 to 350 ??C. Two types of NSOs were recovered: one is soluble in n-pentane and the second in dichloromethane. A kinetic scheme was optimised including both kerogen and NSO cracking. It was validated by complementary experiments carried out on isolated asphaltenes generated from the Type II kerogen and on the total n-pentane and DCM extracts generated from the Type III lignite. Results show that kerogen and lignite first decompose into DCM NSOs with minor generation of hydrocarbons. Then, the main source of petroleum potential originates from secondary cracking of both DCM and n-pentane NSOs through successive decomposition reactions. These results confirm the model proposed by Tissot [Tissot, B., 1969. Premie??res donne??es sur les me??canismes et la cine??tique de la formation du pe??trole dans les bassins se??dimentaires. Simulation d'un sche??ma re??actionnel sur ordinateur. Oil and Gas Science and Technology 24, 470-501] in which the main source of hydrocarbons is not the insoluble organic matter, but the NSO fraction. As secondary cracking of the NSOs largely overlaps that of the kerogen, it was demonstrated that bulk kinetics in open system is a result of both kerogen and NSO cracking. Thus, another kinetic scheme for primary cracking in open system was built as a combination of kerogen and NSO cracking. This new kinetic scheme accounts for both the rate and amounts of hydrocarbons generated in a closed pyrolysis system. Thus, the concept of successive steps for hydrocarbon generation is valid for the two types of pyrolysis system and, for the first time, a common kinetic scheme is available for extrapolating results to natural case studies. ?? 2007 Elsevier Ltd. All rights reserved.

An ecosystem approach to evaluate restoration measures in the lignite mining district of Lusatia/Germany

NASA Astrophysics Data System (ADS)

Schaaf, Wolfgang

2015-04-01

Lignite mining in Lusatia has a history of over 100 years. Open-cast mining directly affected an area of 1000 km2. Since 20 years we established an ecosystem oriented approach to evaluate the development and site characteristics of post-mining areas mainly restored for agricultural and silvicultural land use. Water and element budgets of afforested sites were studied under different geochemical settings in a chronosequence approach (Schaaf 2001), as well as the effect of soil amendments like sewage sludge or compost in restoration (Schaaf & Hüttl 2006). Since 10 years we also study the development of natural site regeneration in the constructed catchment Chicken Creek at the watershed scale (Schaaf et al. 2011, 2013). One of the striking characteristics of post-mining sites is a very large small-scale soil heterogeneity that has to be taken into account with respect to soil forming processes and element cycling. Results from these studies in combination with smaller-scale process studies enable to evaluate the long-term effect of restoration measures and adapted land use options. In addition, it is crucial to compare these results with data from undisturbed, i.e. non-mined sites. Schaaf, W., 2001: What can element budgets of false-time series tell us about ecosystem development on post-lignite mining sites? Ecological Engineering 17, 241-252. Schaaf, W. and Hüttl, R. F., 2006: Direct and indirect effects of soil pollution by lignite mining. Water, Air and Soil Pollution - Focus 6, 253-264. Schaaf, W., Bens, O., Fischer, A., Gerke, H.H., Gerwin, W., Grünewald, U., Holländer, H.M., Kögel-Knabner, I., Mutz, M., Schloter, M., Schulin, R., Veste, M., Winter, S. & Hüttl, R.F., 2011: Patterns and processes of initial terrestrial-ecosystem development. Journal of Plant Nutrition and Soil Science, 174, 229-239. Schaaf, W., Elmer, M., Fischer, A., Gerwin, W., Nenov, R., Pretsch, H. and Zaplate, M.K., 2013: Feedbacks between vegetation, surface structures and hydrology during initial development of the artificial catchment `Chicken Creek'. Procedia Environmental Sciences 19, 86-95.

Infiltration and soil erosion modelling on Lausatian post mine sites

NASA Astrophysics Data System (ADS)

Kunth, Franziska; Schmidt, Jürgen

2013-04-01

Land management of reclaimed lignite mine sites requires long-term and safe structuring of recultivation areas. Erosion by water leads to explicit soil losses, especially on heavily endangered water repellent and non-vegetated soil surfaces. Beyond that, weathering of pyrite-containing lignite burden dumps causes sulfuric acid-formation, and hence the acidification of groundwater, seepage water and surface waters. Pyrite containing sediment is detached by precipitation and transported into worked-out open cuts by draining runoff. In addition to ground water influence, erosion processes are therefore involved in acidification of surface waters. A model-based approach for the conservation of man-made slopes of post mining sites is the objective of this ongoing study. The study shall be completed by modeling of the effectiveness of different mine site recultivation scenarios. Erosion risks on man-made slopes in recultivation areas should be determined by applying the physical, raster- and event based computer model EROSION 2D/3D (Schmidt, 1991, 1992; v. Werner, 1995). The widely used erosion model is able to predict runoff as well as detachment, transport and deposition of sediments. Lignite burden dumps contain hydrophobic substances that cover soil particles. Consequently, these soils show strong water repellency, which influences the processes of infiltration and soil erosion on non-vegetated, coal containing dump soils. The influence of water repellency had to be implemented into EROSION 2D/3D. Required input data for soil erosion modelling (e.g. physical soil parameters, infiltration rates, calibration factors, etc.) were gained by soil sampling and rainfall experiments on non-vegetated as well as recultivated reclaimed mine sites in the Lusatia lignite mining region (southeast of Berlin, Germany). The measured infiltration rates on the non-vegetated water repellent sites were extremely low. Therefore, a newly developed water repellency-factor was applied to depict infiltration and erosion processes on water repellent dump soils. For infiltration modelling with EROSION 2D calibration factors (e.g. water repellency factor, skin-factor, etc.) were determined in different steps by calibrating computer modelled infiltration, respectively volume rate of flow to the measured data.

Groundwater-quality data in the Bear Valley and Selected Hard Rock Areas study unit, 2010: Results from the California GAMA Program

USGS Publications Warehouse

Mathany, Timothy M.; Belitz, Kenneth

2013-01-01

Groundwater quality in the 112-square-mile Bear Valley and Selected Hard Rock Areas (BEAR) study unit was investigated by the U.S. Geological Survey (USGS) from April to August 2010, as part of the California State Water Resources Control Board (SWRCB) Groundwater Ambient Monitoring and Assessment (GAMA) Program’s Priority Basin Project (PBP). The GAMA-PBP was developed in response to the California Groundwater Quality Monitoring Act of 2001 and is being conducted in collaboration with the SWRCB and Lawrence Livermore National Laboratory (LLNL). The BEAR study unit was the thirty-first study unit to be sampled as part of the GAMA-PBP. The GAMA Bear Valley and Selected Hard Rock Areas study was designed to provide a spatially unbiased assessment of untreated-groundwater quality in the primary aquifer system and to facilitate statistically consistent comparisons of untreated groundwater quality throughout California. The primary aquifer system is defined as the zones corresponding to the perforation intervals of wells listed in the California Department of Public Health (CDPH) database for the BEAR study unit. Groundwater quality in the primary aquifer system may differ from the quality in the shallow or deep water-bearing zones; shallow groundwater may be more vulnerable to surficial contamination. In the BEAR study unit, groundwater samples were collected from two study areas (Bear Valley and Selected Hard Rock Areas) in San Bernardino County. Of the 38 sampling sites, 27 were selected by using a spatially distributed, randomized grid-based method to provide statistical representation of the primary aquifer system in the study unit (grid sites), and the remaining 11 sites were selected to aid in the understanding of the potential groundwater-quality issues associated with septic tank use and with ski areas in the study unit (understanding sites). The groundwater samples were analyzed for organic constituents (volatile organic compounds [VOCs], pesticides and pesticide degradates, pharmaceutical compounds, and wastewater indicator compounds [WICs]), constituents of special interest (perchlorate, N-nitrosodimethylamine [NDMA], and 1,2,3-trichloropropane [1,2,3-TCP]), and inorganic constituents (trace elements, nutrients, dissolved organic carbon [DOC], major and minor ions, silica, total dissolved solids [TDS], alkalinity, and arsenic and iron species), and uranium and other radioactive constituents (radon-222 and activities of tritium and carbon-14). Isotopic tracers (of hydrogen and oxygen in water, of nitrogen and oxygen in dissolved nitrate, of dissolved boron, isotopic ratios of strontium in water, and of carbon in dissolved inorganic carbon) and dissolved noble gases (argon, helium-4, krypton, neon, and xenon) were measured to help identify the sources and ages of sampled groundwater. In total, groundwater samples were analyzed for 289 unique constituents and 8 water-quality indicators in the BEAR study unit. Quality-control samples (blanks, replicate pairs, or matrix spikes) were collected at 13 percent of the sites in the BEAR study unit, and the results for these samples were used to evaluate the quality of the data from the groundwater samples. Blank samples rarely contained detectable concentrations of any constituent, indicating that contamination from sample collection or analysis was not a significant source of bias in the data for the groundwater samples. Replicate pair samples all were within acceptable limits of variability. Matrix-spike sample recoveries were within the acceptable range (70 to 130 percent) for approximately 84 percent of the compounds. This study did not evaluate the quality of water delivered to consumers. After withdrawal, groundwater typically is treated, disinfected, and (or) blended with other waters to maintain water quality. Regulatory benchmarks apply to water that is delivered to the consumer, not to untreated groundwater. However, to provide some context for the results, concentrations of constituents measured in the untreated groundwater were compared with regulatory and non-regulatory health-based benchmarks established by the U.S. Environmental Protection Agency (USEPA) and CDPH, and to non-health-based benchmarks established for aesthetic concerns by CDPH. Comparisons between data collected for this study and benchmarks for drinking water are for illustrative purposes only and are not indicative of compliance or non-compliance with those benchmarks. All concentrations of organic and special-interest constituents from grid sites sampled in the BEAR study unit were less than health-based benchmarks. In total, VOCs were detected in 17 of the 27 grid sites sampled (approximately 63 percent), pesticides and pesticide degradates were detected in 4 grid sites (approximately 15 percent), and perchlorate was detected in 21 grid sites (approximately 78 percent). Inorganic constituents (trace elements, major and minor ions, nutrients, and uranium and other radioactive constituents) were sampled for at 27 grid sites; most concentrations were less than health-based benchmarks. Exceptions include one detection of arsenic greater than the USEPA maximum contaminant level (MCL-US) of 10 micrograms per liter (μg/L), three detections of uranium greater than the MCL-US of 30 μg/L, nine detections of radon-222 greater than the proposed MCL-US of 4,000 picocuries per liter (pCi/L), and one detection of fluoride greater than the CDPH maximum contaminant level (MCL-CA) of 2 milligrams per liter. Concentrations of inorganic constituents with non-health-based benchmarks (iron, manganese, chloride, and TDS) were less than the CDPH secondary maximum contaminant level (SMCL-CA) in most grid sites. Exceptions include two detections of iron greater than the SMCL-CA of 300 μg/L and one detection of manganese greater than the SMCL-CA of 50 μg/L.

Radioactive rare-earth deposit at Scrub Oaks mine, Morris County, New Jersey

USGS Publications Warehouse

Klemic, Harry; Heyl, A.V.; Taylor, Audrey R.; Stone, Jerome

1959-01-01

A deposit of rare-earth minerals in the Scrub Oaks iron mine, Morris County, N. J., was mapped and sampled in 1955. The rare-earth minerals are mainly in coarse-grained magnetite ore and in pegmatite adjacent to it. Discrete bodies of rare-earth-bearing magnetite ore apparently follow the plunge of the main magnetite ore body at the north end of the mine. Radioactivity of the ore containing rare earths is about 0.2 to 0.6 mllliroentgens per hour. The principal minerals of the deposit are quartz, magnetite, hematite, albiteoligoclase, perthite and antiperthite. Xenotime and doverite aggregates and bastnaesite with intermixed leucoxene are the most abundant rare-earth minerals, and zircon, sphene, chevkinite, apatite, and monazite are of minor abundance in the ore. The rare-earth elements are partly differentiated into cerium-rich bastnaesite, chevkinite, and monazite, and yttrium-rich xenotime and doverite. Apatite, zircon, and sphene contain both cerium and yttrium group earths. Eleven samples of radioactive ore and rock average 0.009 percent uranium, 0.062 percent thorium, 1.51 percent combined rare-earth oxides including yttrium oxide and 24.8 percent iron. Scatter diagrams of sample data show a direct correlation between equivalent uranium, uranium, thorium, and combined rare^ earth oxides. Both cerium- and yttrium-group earths are abundant in the rare-earth minerals. Radioactive magnetite ore containing rare-earth minerals probably formed as a variant of the magnetite mineralization that produced the main iron ore of the Scrub Oaks deposit. The rare-earth minerals and the iron ore were deposited contemporaneously. Zircon crystals, probably deposited at the same time, have been determined by the Larsen method to be about 550 to 600 million years old (late Precambrian age). Uranium, thorium, and rare-earth elements are potential byproducts of iron in the coarse-grained magnetite ore.

Microbial desulphurization of Turkish lignites by White Rot Fungi

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

Pinar Aytar; Mesut Sam; Ahmet Cabuk

2008-03-15

Biodesulphurization experiments were carried out with Tuncbilek lignite, characterized by high sulfur content (2.59%) by using Trametes versicolor ATCC 200801 and Phanerochaete chrysosporium ME 446. At fungal biomass studies, the effects of various parameters on fungal desulphurization of coals such as pH, temperature, pulp density, incubation time, and sterilization were investigated for both microorganisms. The maximum desulphurization (40%) was observed after 6 days of incubation at 35{sup o}C for T. versicolor. The optimum pH was measured at 6, and the agitation rate was fixed at 125 rpm. The pulp density was found as 5% (w/v) for the high extent ofmore » desulphurization. Also, calorific value did not change during this experiment. However, the ash and metal contents of coal were eliminated. 30 refs., 6 figs., 2 tabs.« less

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

NONE

ARCTECH has developed a novel process (MicGAS) for direct, anaerobic biomethanation of coals. Biomethanation potential of coals of different ranks (Anthracite, bitumious, sub-bitumious, and lignites of different types), by various microbial consortia, was investigated. Studies on biogasification of Texas Lignite (TxL) were conducted with a proprietary microbial consortium, Mic-1, isolated from hind guts of soil eating termites (Zootermopsis and Nasutitermes sp.) and further improved at ARCTECH. Various microbial populations of the Mic-1 consortium carry out the multi-step MicGAS Process. First, the primary coal degraders, or hydrolytic microbes, degrade the coal to high molecular weight (MW) compounds. Then acedogens ferment themore » high MW compounds to low MW volatile fatty acids. The volatile fatty acids are converted to acetate by acetogens, and the methanogens complete the biomethanation by converting acetate and CO{sub 2} to methane.« less

The use of Pb isotopes to differentiate between contemporary and ancient sources of pollution in Greece

NASA Astrophysics Data System (ADS)

Åberg, G.; Charalampides, G.; Fosse, G.; Hjelmseth, H.

Stable lead isotopes are used to illustrate the relation source-receptor and to differentiate between sources of pollution in Greece. Air filters collected in the Kozani-Ptolemais lignite mining area, West Macedonia, point to an impact from gasoline lead as well as lead from the combustion of lignite. This is supported by lead isotope data of wheat grown on reclaimed land. Lead isotope analyses of contemporary teeth from the Lavrio sulphide mining area, southeast of Greece, show the imprint of previous mining activities as well as traffic emissions. Moreover, the Lavrio teeth can be distinguished from one tooth from Athens; the Athens tooth show a stronger impact of gasoline lead. Lead data also imply that the Greek top soil is contaminated by air pollution from earlier sulphide mining and smelting since Hellenic and Roman times.

Preliminary report on the lignite resources of the Niobe area, Burke and Ward counties, North Dakota

USGS Publications Warehouse

Owen, Hal E.

1977-01-01

Two lignite beds, the Niobe and the Bonus, occur at strippable depths within the Niobe area. The Niobe bed averages 5 feet (1.5 meters) in thickness and the Bonus bed averages 8 feet (2.4 meters) in thickness. These beds lie in the lower part of the Sentinel Butte Member of the Fort Union Formation (Paleocene). The demonstrated resources of both beds combined is 122 million tons (110 million tonnes), all of which are under less than 120 feet (37 meters) of overburden. The overburden consists of glacial till and shale. The lateral continuity of the coal has been locally interrupted by faulting, glacial outwash channels, and erosion. Folding and/or faulting occurs parallel to the Missouri Coteau escarpment and faulting occurs roughly perpendicular to the escarpment.

Catalysts and process developments for two-stage liquefaction. First quarterly technical progress report No. 52, October 1, 1991--December 31, 1991

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

Cronauer, D.C.; Swanson, A.J.; Sajkowski, D.J.

Research under way in this project centers upon developing and evaluating catalysts and process improvements for coal liquefaction in the two-stage, close-coupled catalytic process. As discussed in the previous quarterly report, the feedstock liquefaction studies for the three feedstocks (Black Thunder subbituminous coal, Martin Lake lignite, and Illinois No. 6 coal) were completed. Both Black Thunder coal and Martin Lake lignite gave lighter products than Illinois No. 6 coal at similar process conditions. Severe catalyst deactivation in the first stage was also observed with the Martin Lake lignite run. The first stage catalyst testing program was started (Task 3.2.1). Aftermore » a successful reference run with Illinois No. 6 coal, a high-temperature run with AMOCAT{trademark} 1C was completed, where the results showed that the first stage temperature should be no higher than 820{degrees}F. In addition, several runs were made both with Illinois No. 6 and Black Thunder coals using oil-soluble catalysts, Molyvan L, and molybdenum octoate in one or both stages. Overall, the results look very promising and show that dispersed molybdenum catalysts are good alternatives for Stage 1 or both 1 and 2, especially for Illinois No. 6 coal. In the case of Black Thunder coal, the conversion and yields were good, although the product quality was poorer, however, the use of slurry catalysts is still recommended.« less

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

Ali Sinag; Melike Sungur; Muammer Canel

Copyrolysis of a Turkish lignite with low-density polyethylene (LDPE) is conducted in a tubular reactor. The effect of experimental conditions (temperature of 400-700{sup o}C, catalyst, LDPE contents of the mixture are 33, 50, and 67 wt %) on the formation of tar, gas, and char and their effects on the formation of phenol are investigated. The catalysts used are red mud (which is a waste product of an aluminum factory in Turkey), zeolite (Linde type A (LTA)), and K{sub 2}CO{sub 3}. Tar evolution is determined to be increased significantly by increasing the LDPE content of the coal-LDPE mixture during themore » pyrolysis. The effect of adding LDPE to the coal on the gas generation is not remarkable. An increase in temperature leads to increased gas yields. Phenol and phenol derivatives are the obstacles for the complete conversion of lignite to tar and gas. To investigate this negative effect of phenols on the yields, the phenols found in tar from coal pyrolysis are detected by gas chromatography-mass spectroscopy (GC-MS), and it is observed that phenolic structures detected in the tar obtained by individual pyrolysis of coal are dramatically decreased by adding polymer to the coal. The use of catalysts during the copyrolysis procedure leads to improved gas generation. The possible reasons of these variations are discussed. A remarkable synergetic effect between lignite and LDPE on the tar yields is also observed. 21 refs., 8 figs., 4 tabs.« less

Modification of apparent fission yields by Chemical Fractionation following Fission (CFF)

NASA Astrophysics Data System (ADS)

Hohenberg, Charles; Meshik, Alex

2008-04-01

Grain-by-grain studies of the 2 billion year old Oklo natural reactor, using laser micro-extraction^1,2, yield detailed information about Oklo, a water-moderated pulsed reactor, cycle times, total neutron fluence and duration, but it also demonstrates Chemical Fractionation following Fission. In the CFF process, members of an isobaric yield chain with long half-lives are subject to migration before decay can occur. Of particular interest is the 129 isobar where 17 million ^129I can migrate out of the host grain before decay, and iodine compounds are water soluble. This is amply demonstated by the variation of Xe spectra between micron-sized uranium-bearing minerals and adjacent uranium-free minerals. Fission 129 yields for the spontaneous fission of ^238U generally come from measured ^129Xe in pitchblend^2, ores emplaced by aqueous activity, and are incorrect due to the CFF process. ^238U yields for the 131 and 129 chains, reported in Hyde^3, as 0.455 +- .02 and < 0.012, respectively, the latter being anomalously low. ^1A Meshik, C Hohenberg and O Pravdivtesva, PRL 93, 182302 (2004); A Meshik Sci. Am. Nov (2005), 55; ^2E K Hyde, Nucl Prop of Heavy Elements III (1964).

RECOVERY OF URANIUM FROM LOW GRADE URANIUM BEARING ORES

DOEpatents

Rhodes, H.B.; Pesold, W.F.; Hirshon, J.M.

1959-06-01

Recovery of U, Fe, and Al from Chattanooga shale is described. Ground shale (-4 to +325 mesh) is roasted to remove organic and volatile matter. The heated shale is then reacted with a chlorinating agent (CCl/sub 4/, COCl/sub 2/, Cl, and SCl) at 600 to 1000 C. The metal chloride vapor is separated from entrained solids and then contacted with a liquid alkali metal chloride which removes U. The U is reeovered by cooling and dissolving the bath followed by acidification and solvent extraction. A condensed phase of Al, Fe, and K chlorides is treated to separate Al as alumina by passing through a Fe/sub 2/O/ sub 3/ bed. The remaining FeCl/sub 3/ is oxidized by O/sub 2/ at 1000 C to form Fe/sub 2/O/sub 3/ and Cl/sub 2/. Alternatively, vapor from the U separation step may be passed to a liquid KCl bath at 500 to 650 C. The resulting mixture is oxidized to form Cl/sub 2/ and Fe/sub 2/O/sub 3/ + Al/sub 2/O/sub 3/. The Al and Fe are separated by reaction with NaOH at high temperatures and pressures. (T.R.H.)

Some thorium prospects, Lemhi Pass area, Beaverhead County, Montana

USGS Publications Warehouse

Armstrong, Frank C.

1955-01-01

The Last Chance group> Brown Bear and Shady Tree claims in Beaverhead County, Mont., were explored for thorium under a Defense Minerals Exploration Administration Contract in 1951 and 1952. The project was undertaken to explore northwest-trending moderately to steep dipping, thorite-bearing quartz-barite-hematite veins. The veins are wall-rock replacements and fissure fillings in faults and shears that cut rocks of the Precambrian Belt series. Recurrent movement along the faults has intense fractured the veins. Quartz iron-oxide minerals, and thorite have been deposited in these fractures. The iron oxides and thorite are intimately associated and were among the last minerals deposited. Because no rare earth or uranium minerals have been found in the veins, it is thought that the small amounts of these elements reported in the analyses must substitute for thorium in the thorite. Under the D. M. E. A. contract the Last Chance vein was traced on surface for a distance of about 1,300 feet; the thickness ranges from about 35 feet to a few inches. Two diamond drill holes cut the vein 240 and 290 feet below the outcrop.

Subsurface Conditions Controlling Uranium Incorporation in Iron Oxides: A Redox Stable Sink

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

Fendorf, Scott

2016-04-05

Toxic metals and radionuclides throughout the U.S. Department of Energy Complex pose a serious threat to ecosystems and to human health. Of particular concern is the redox-sensitive radionuclide uranium, which is classified as a priority pollutant in soils and groundwaters at most DOE sites owing to its large inventory, its health risks, and its mobility with respect to primary waste sources. The goal of this research was to contribute to the long-term mission of the Subsurface Biogeochemistry Program by determining reactions of uranium with iron (hydr)oxides that lead to long-term stabilization of this pervasive contaminant. The research objectives of thismore » project were thus to (1) identify the (bio)geochemical conditions, including those of the solid-phase, promoting uranium incorporation in Fe (hydr)oxides, (2) determine the magnitude of uranium incorporation under a variety of relevant subsurface conditions in order to quantify the importance of this pathway when in competition with reduction or adsorption; (3) identify the mechanism(s) of U(VI/V) incorporation in Fe (hydr)oxides; and (4) determine the stability of these phases under different biogeochemical (inclusive of redox) conditions. Our research demonstrates that redox transformations are capable of achieving U incorporation into goethite at ambient temperatures, and that this transformation occurs within days at U and Fe(II) concentrations that are common in subsurface geochemical environments with natural ferrihydrites—inclusive of those with natural impurities. Increasing Fe(II) or U concentration, or initial pH, made U(VI) reduction to U(IV) a more competitive sequestration pathway in this system, presumably by increasing the relative rate of U reduction. Uranium concentrations commonly found in contaminated subsurface environments are often on the order of 1-10 μM, and groundwater Fe(II) concentrations can reach exceed 1 mM in reduced zones of the subsurface. The redox-driven U(V) incorporation mechanism may help to explain U retention in some geologic materials, improving our understanding of U-based geochronology and the redox status of ancient geochemical environments. Additionally, U(VI) may be incorporated within silicate minerals though encapsulation of U-bearing iron oxides, leading to a redox stable solid. Our research detailing previously unrecognized mechanism of U incorporation within sediment minerals may even lead to new approaches for in situ contamination remediation techniques, and will help refine models of U fate and transport in reduced subsurface zones.« less

Processing of solid solution, mixed uranium/refractory metal carbides for advanced space nuclear power and propulsion systems

NASA Astrophysics Data System (ADS)

Knight, Travis Warren

Nuclear thermal propulsion (NTP) and space nuclear power are two enabling technologies for the manned exploration of space and the development of research outposts in space and on other planets such as Mars. Advanced carbide nuclear fuels have been proposed for application in space nuclear power and propulsion systems. This study examined the processing technologies and optimal parameters necessary to fabricate samples of single phase, solid solution, mixed uranium/refractory metal carbides. In particular, the pseudo-ternary carbide, UC-ZrC-NbC, system was examined with uranium metal mole fractions of 5% and 10% and corresponding uranium densities of 0.8 to 1.8 gU/cc. Efforts were directed to those methods that could produce simple geometry fuel elements or wafers such as those used to fabricate a Square Lattice Honeycomb (SLHC) fuel element and reactor core. Methods of cold uniaxial pressing, sintering by induction heating, and hot pressing by self-resistance heating were investigated. Solid solution, high density (low porosity) samples greater than 95% TD were processed by cold pressing at 150 MPa and sintering above 2600 K for times longer than 90 min. Some impurity oxide phases were noted in some samples attributed to residual gases in the furnace during processing. Also, some samples noted secondary phases of carbon and UC2 due to some hyperstoichiometric powder mixtures having carbon-to-metal ratios greater than one. In all, 33 mixed carbide samples were processed and analyzed with half bearing uranium as ternary carbides of UC-ZrC-NbC. Scanning electron microscopy, x-ray diffraction, and density measurements were used to characterize samples. Samples were processed from powders of the refractory mono-carbides and UC/UC 2 or from powders of uranium hydride (UH3), graphite, and refractory metal carbides to produce hypostoichiometric mixed carbides. Samples processed from the constituent carbide powders and sintered at temperatures above the melting point of UC showed signs of liquid phase sintering and were shown to be largely solid solutions. Pre-compaction of mixed carbide powders prior to sintering was shown to be necessary to achieve high densities. Hypostoichiometric, samples processed at 2500 K exhibited only the initial stage of sintering and solid solution formation. Based on these findings, a suggested processing methodology is proposed for producing high density, solid solution, mixed carbide fuels. Pseudo-binary, refractory carbide samples hot pressed at 3100 K and 6 MPa showed comparable densities (approximately 85% of the theoretical value) to samples processed by cold pressing and sintering at temperatures of 2800 K.

Genesis of kasolite associated with aplite-pegmatite at Jabal Sayid, Hijaz region, Kingdom of Saudi Arabia

NASA Astrophysics Data System (ADS)

Dawood, Yehia H.; Harbi, Hesham M.; Abd El-Naby, Hamdy H.

2010-01-01

In this study, we report kasolite Pb(UO 2)SiO 4·(H 2O) for the first time as a main uranyl mineral in the mineralized aplite-pegmatite of Jabal Sayid, Hijaz region. It commonly forms clusters of yellow acicular crystals in the voids and fractures. The mineral chemistry and mineralogical characteristics of kasolite were investigated using different techniques. Calcium, iron and phosphorus are detected in kasolite in addition to its major constituents; uranium, lead and silicon. Lead does not exist as a radiogenic product and not even as a substitute for uranium in the mineral structure. Alternatively, galena mineralization could be considered as a source for lead. The fluoride and carbonate complexes played a significant role in the formation of kasolite. High temperature hydrothermal solutions reacted with pre-existing uranium-bearing metamictized accessory minerals such as pyrochlore, U-rich thorite and zircon to form uranous fluoride complexes. These complexes are predominant in reducing environment and at pH 4. When the fluids approached the surface passing through fracture system, the oxygen fugacity ( fO 2) and the pH increased because of the loss of volatile components. At these conditions, uranous fluorides would convert to uranyl fluoride complexes UO 2F 3-. Further decrease in temperature was associated with the decay of the activity of fluorine ion by the dilution of hydrothermal solutions and precipitation of fluorite. At this condition, uranyl-carbonate complexes are favoured. These complexes were combined later with silica and lead to form kasolite.

Summary of reconnaissance for radioactive deposits in Alaska, 1945-1954, and an appraisal of Alaskan uranium possibilities

USGS Publications Warehouse

Wedow, Helmuth

1956-01-01

In the period 1945-1954 over 100 investigations for radioactive source materials were made in Alaska. The nature of these investigations ranged from field examinations of individual prospects or the laboratory analysis of significantly radioactive samples submitted by prospectors to reconnaissance studies of large districts. In this period no deposits of uranium or thorium that would warrant commercial exploitation were discovered. The investigations, however, disclosed that radioactive materials occur in widely scattered areas of Alaska and in widely diverse environments. Many igneous rocks throughout Alaska are weakly radioactive because of uranium- and thorium-bearing accessory minerals, such as allanite, apatite, monazite, sphene, xenotime, and zircon; more rarely the radioactivity of these rocks is due to thorianite or thorite and their uranoan varieties. The felsic rocks, for example, granites and syenites, are generally more radioactive than the mafic igneous rocks. Pegmatites, locally, have also proved to be radioactive, but they have little commercial significance. No primary uranium oxide minerals have been found yet in Alaskan vein deposits, except, perhaps, for a mineral tentatively identified as pitchblende in the Hyder district of southeastern Alaska. However, certain occurrences of secondary uranium minerals, chiefly those of the uranite group, on the Seward Peninsula, in the Russian Mountains, and in the vicinity of Kodiak suggest that pitchblende-type ores may occur at depth beneath zones of alteration. Thorite-bearing veins have been discovered on Prince of Wales Island in southeastern Alaska. Although no deposits or carnotite-type minerals have been found in Alaska, several samples containing such minerals have been submitted by Alaskan prospectors. Efforts to locate the deposits from which these minerals were obtained have been unsuccessful, but review of available geologic data suggests that several Alaskan areas are potentially favorable for carnotite-type deposits. The chief of these areas is the Alaska Peninsula-Cook Inlet area which encompasses most of the reported occurrences of the prospectors' carnotite-type samples. Alaska is also potentially favorable for the occurrence of large bodies of the very low-grade uraniferous sedimentary rocks, such as phosphorites and black shales. This type of deposit, however, has not received much study because of the emphasis on the search for bonanza-type high-grade ores. Uraniferous phosphorites similar to those of Idaho, Montana, and Wyoming occur in northern Alaska on the north flank of the Brooks Range; black shales comparable to the uraniferous shales of the Chattanooga formation of southeastern United States have been noted along the Yukon River near the international boundary. Placer deposits in Alaska have some small potential for the production of the radioactive elements as byproducts of gold- and tin-placer mining. the placer area believed to have the relatively greatest potential in Alaska lies in the Kahiltna River valley where concentrates are known to contain such commercial minerals as ilmenite, cassiterite, platinum, and gold in addition to uranothorianite and monazite. The possibilities of the natural fluids--water and petroleum--have not yet been tested in Alaska to any great extent. Studies of fluids are in progress to determine whether they may be used to discover and define areas potentially favorable for the occurrence of uraniferous lodes.

30 CFR 90.2 - Definitions.

Code of Federal Regulations, 2012 CFR

2012-07-01

... old section 203(b) program (36 FR 20601, October 27, 1971), or under § 90.3 (Part 90 option; notice of... area bituminous coal, lignite, or anthracite from its natural deposits in the earth by any means or...

30 CFR 90.2 - Definitions.

Code of Federal Regulations, 2013 CFR

2013-07-01

... old section 203(b) program (36 FR 20601, October 27, 1971), or under § 90.3 (Part 90 option; notice of... area bituminous coal, lignite, or anthracite from its natural deposits in the earth by any means or...

30 CFR 90.2 - Definitions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... old section 203(b) program (36 FR 20601, October 27, 1971), or under § 90.3 (Part 90 option; notice of... area bituminous coal, lignite, or anthracite from its natural deposits in the earth by any means or...

30 CFR 90.2 - Definitions.

Code of Federal Regulations, 2010 CFR

2010-07-01

... old section 203(b) program (36 FR 20601, October 27, 1971), or under § 90.3 (Part 90 option; notice of... area bituminous coal, lignite, or anthracite from its natural deposits in the earth by any means or...

30 CFR 90.2 - Definitions.

Code of Federal Regulations, 2014 CFR

2014-07-01

... old section 203(b) program (36 FR 20601, October 27, 1971), or under § 90.3 (Part 90 option; notice of... area bituminous coal, lignite, or anthracite from its natural deposits in the earth by any means or...

Corrosion Testing of 304L SS 3013 Inner Container and Teardrop Samples

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

Tokash, Justin Charles; Hill, Mary Ann; Lillard, Scott

The Department of Energy (DOE) 3013 Standard specifies a minimum of two containers to be used for the storage of plutonium-bearing materials containing at least 30 wt.% plutonium and uranium. Three nested containers are typically used, the outer, inner, and convenience containers, shown in Figure 1. Both the outer and inner containers are sealed with a weld while the innermost convenience container must not be sealed. Lifetime of the containers is expected to be fifty years. The containers are fabricated of austenitic stainless steels (SS) due to their high corrosion resistance. Potential failure mechanisms of the storage containers have beenmore » examined by Kolman and Lillard et al.« less

Bearing assembly and the like for use in corrosive and non-corrosive atmospheres

DOEpatents

Mashburn, Douglas N.; Woodall, Harold C.; Wright, Ralph R.

1979-01-01

This invention relates to a novel machine element characterized by mutually rubbing surfaces which are composed of dissimilar materials having high hardness, a low coefficient of friction, and resistance to corrosion by halogen-containing atmospheres. As exemplified by the preferred embodiment for use in gaseous UF.sub.6, the rubbing surfaces are chemically deposited nickel and anodized aluminum. These surfaces permit jam-free operation despite long-term exposure to UF.sub.6. Preferably, both surfaces have a hardness of at least about 500 HV.sub.100 on the Vickers hardness scale, and preferably the anodized-aluminum surface is of a type having comparatively little tendency to sorb uranium hexafluoride.

Uranium-Bearing Srilankite from High-Pressure Garnetites of the Southern Urals: First Data

NASA Astrophysics Data System (ADS)

Gottman, I. A.; Pushkarev, E. V.; Khiller, V. V.

2018-04-01

This work presents the results of studying srilankite, a rare zirconium titanate (ZrTi2O6), associated with ilmenite, rutile, zircon, uraninite, and other minerals discovered in high-pressure garnetites of the lherzolite Mindyak massif (Southern Urals). Srilankite occurs as inclusions in ilmenite and rutile of up to several tens of microns in size. It was established for the first time that srilankite contains a significant UO2 admixture (up to 20%). The negative correlation between Zr and U is evidence of isomorphism in the srilankite-brannerite system. The association of srilankite with high-Zr rutile indicates that formation of these minerals occurred at T > 850°C.

Evaluation of Rare Earth Element Extraction from North Dakota Coal-Related Feed Stocks

NASA Astrophysics Data System (ADS)

Laudal, Daniel A.

The rare earth elements consist of the lanthanide series of elements with atomic numbers from 57-71 and also include yttrium and scandium. Due to their unique properties, rare earth elements are crucial materials in an incredible array of consumer goods, energy system components and military defense applications. However, the global production and entire value chain for rare earth elements is dominated by China, with the U.S. currently 100% import reliant for these critical materials. Traditional mineral ores including previously mined deposits in the U.S., however, have several challenges. Chief among these is that the content of the most critical and valuable of the rare earths are deficient, making mining uneconomical. Further, the supply of these most critical rare earths is nearly 100% produced in China from a single resource that is only projected to last another 10 to 20 years. The U.S. currently considers the rare earths market an issue of national security. It is imperative that alternative domestic sources of rare earths be identified and methods developed to produce them. Recently, coal and coal byproducts have been identified as one of these promising alternative resources. This dissertation details a study on evaluation of the technical and economic feasibility of rare earth element recovery from North Dakota lignite coal and lignite-related feedstocks. There were four major goals of this study: i) identify lignite or lignite-related feedstocks with total rare earth element content above 300 parts per million, a threshold dictated by the agency who funded this research as the minimum for economic viability, ii) determine the geochemistry of the feedstocks and understand the forms and modes of occurrence of the rare earth elements, information necessary to inform the development of extraction and concentration methods, iii) identify processing methods to concentrate the rare earth elements from the feedstocks to a target of two weight percent, a value that would be sufficient to leverage existing separation and refining methods developed for the traditional mineral ore industry, and iv) develop a process that is economically viable and environmentally benign. To achieve these overall goals, and to prove or disprove the research hypotheses, the research scope was broken down into three main efforts: i) sampling and characterization of potential feedstocks, ii) laboratory-scale development and testing of rare earth element extraction and concentration methods, and iii) process design and technical and economic feasibility evaluation. In total, 174 unique samples were collected, and several locations were identified that exceeded the 300 ppm total rare earth elements target. The results showed that on a whole sample basis, the rare earths are most concentrated in the clay-rich sediments associated with the coal seams, but on an ash basis in certain locations within certain coal seams the content is significantly higher, an unexpected finding given prior research. At Falkirk Mine near Underwood, North Dakota three coal seams were found to have elevated levels of rare earths, ranging from about 300 to 600 ppm on an ash basis. Additionally, exceptionally high rare earths content was found in samples collected from an outcropping of the Harmon-Hansen coal zone in southwestern North Dakota that contained 2300 ppm on an ash basis. The results dictated that extraction and concentration methods be developed for these rare earth element-rich coals, instead of the mineral-rich sediments. This effort also found that at a commercial-scale, due to non-uniformity of the rare earths content stratigraphically in the coal seams, selective mining practices will be needed to target specific locations within the seams. The bulk mining and blending practices as Falkirk Mine result in a relatively low total rare earths content in the feed coal entering the Coal Creek Power Station adjacent to the mine. Characterization of the coal samples identified that the predominant modes of rare earths occurrence in the lignite coals are associations with the organic matter, primarily as coordination complexes and a lesser amount as ion-exchangeable cations on oxygen functional groups. Overall it appears that about 80-95% of rare earths content in North Dakota lignite is organically associated, and not present in mineral forms, which due to the weak organic bonding, presented a unique opportunity for extraction. The process developed for extraction of rare earths was applied to the raw lignite coals instead of fly ash or other byproducts being investigated extensively in the literature. Rather, the process uses a dilute acid leaching process to strip the organically associated rare earths from the lignite with very high efficiency of about 70-90% at equilibrium contact times. Although the extraction kinetics are quite fast given commercial leaching operations, there is some tradeoff between extraction efficiency and contact time. (Abstract shortened by ProQuest.).

Liberation of microbial substrates from macromolecular organic matter by non-supercritical CO2

NASA Astrophysics Data System (ADS)

Sauer, P.; Glombitza, C.; Kallmeyer, J.

2012-12-01

The worldwide search for suitable underground storage formations for CO2 also considers coal-bearing strata. CO2 is already injected into coal seams for enhanced recovery of coal bed methane. However, the geochemical and microbiological effects of increased CO2 concentrations on organic matter rich formations are rarely investigated. The injected CO2 will dissolve in the pore water, causing a decrease in pH and resulting in acidic formation waters. Low molecular weight organic acids (LMWOAs) are chemically bound to the macromolecular matrix of sedimentary organic matter and may be liberated by hydrolysis, which is enhanced under acidic conditions. Recent investigations outlined the importance of LMWOAs as a feedstock for subsurface microbial life [1]. Therefore, injection of CO2 into coal formations may result in enhanced nutrient supply for subsurface microbes. To investigate the effects of highly CO2-saturated waters on the release of LMWOAs from coal, we developed an inexpensive high-pressure-high-temperature system that allows manipulating the concentration of dissolved gases up to 60 MPa and 120°C, respectively. The sample is placed in a flexible, gas-tight and inert PVDF sleeve, separating it from the pressure fluid and allowing for subsampling without loss of pressure. Lignite samples from the DEBITS-1 well, Waikato Basin, NZ and the Welzow-Süd open-cast mine, Niederlausitz, Germany, were extracted at 90° C and 5 MPa, with either pure water, CO2-saturated water, CO2/NO2 or CO2/SO2-saturated water. Subsamples were taken at different time points during the 72 hrs. long extraction. Extraction of LMWOAs from coal samples with our pressurised system resulted in yields that were up to four times higher than those reported for Soxhlet extraction [2]. These higher yields may be explained by the fact that during Soxhlet extraction the sample only gets into contact with freshly distilled water, whereas in our system the extraction fluid is circulated, resulting in more acidic extraction conditions. In comparison to pure water extractions, CO2-saturated water affected the extraction yield in both directions by up to 40 percent. For the lignite from DEBITS-1 well, CO2-saturated water resulted in a permanently lower yield, whereas the lignites from the Lausitz showed an increase in formate and a decrease in oxalate. LMWOAs found in the extraction fluid may not just result from hydrolysis but also from different secondary reactions. It was suggested that oxalate in aqueous extracts of coals is a result of the decomposition of 1,2-dihydroxy-carboxylic acids [3]. We assume that for oxalate (and maybe for other LMWOAs as well) the extraction yield is not only affected by hydrolysis but also by secondary reactions, which may be suppressed in the presence of CO2 and other gasses dissolved in the extraction medium. These results show the importance of performing laboratory simulations of subsurface processes under conditions that resemble the true in-situ conditions as closely as possible. References [1] Glombitza et al., 2009, Org. Geochem. 40, 175-183 [2] Vieth et al., 2008, Org. Geochem. 39, 985-991 [3] Bou-Raad et al., 2000, Fuel 79, 1185-1193

Graphic and algebraic solutions of the discordant lead-uranium age problem

USGS Publications Warehouse

Stieff, L.R.; Stern, T.W.

1961-01-01

Uranium-bearing minerals that give lead-uranium and lead-lead ages that are essentially in agreement, i.e. concordant, generally are considered to have had a relatively simple geologic history and to have been unaltered since their deposition. The concordant ages obtained on such materials are, therefore, assumed to approach closely the actual age of the minerals. Many uranium-bearing samples, particularly uranium ores, give the following discordant age sequences; Pb206 U238 < Pb207 U235 ??? Pb207 Pb206 or, less frequently, Pb207 Pb206 ??? Pb207 U235 < Pb206 U238. These discordant age sequences have been attributed most often to uncertainties in the common lead correction, selective loss of radio-active daughter products, loss or gain of lead or uranium, or contamination by an older generation of radiogenic lead. The evaluation of discordant lead isotope age data may be separated into two operations. The first operation, with which this paper is concerned, is mechanical in nature and involves the calculation of the different possible concordant ages corresponding to the various processes assumed to have produced the discordant ages. The second operation is more difficult to define and requires, in part, some personal judgement. It includes a synthesis of the possible concordant age solutions with other independent geologic and isotopic evidence. The concordant age ultimately chosen as most acceptable should be consistent not only with the known events in the geologic history of the area, the age relations of the enclosing rocks, and the mineralogic and paragenetic evidence, but also with other independent age measurements and the isotopic data obtained on the lead in related or associated non-radioactive minerals. The calculation of the possible concordant ages from discordant age data has been greatly simplified by Wetherill's graphical method of plotting the mole ratios of radiogenic Pb206 U238 ( N206 N238) vs. radiogenic Pb207 U235 ( N207 N235) after correcting for the contaminating common Pb206 and Pb207. The linear relationships noted in this graphical procedure have been extended to plots of the mole ratios of total Pb206 U238 ( tN206 N238) vs. total Pb207 U235 ( tN207 N235). This modification permits the calculation of concordant ages for unaltered samples using only the Pb207 Pb206 ratio of the contaminating common lead. If isotopic data are available for two samples of the same age, x and y, from the same or related deposits or outcrops, graphs of the normalized difference ratios [ ( N206 N204)x - ( N206 N204)y ( N238 N204)x -( N238 N204)y] vs. [ ( N207 N204)x - ( N207 N204)y ( N235 N204)x -( N235 N204)y] can give concordant ages corrected for unknown amounts of a common lead with an unknown Pb207/ Pb206 ratio. (If thorium is absent the difference ratios may be normalized with the more abundant index isotope, Pb208.) Similar plots of tho normalized, difference ratios for three genetically related samples (x - y) and(x - z), will give concordant ages corrected, in addition, for either one unknown period of past alteration or initial contamination by an older generation of radiogenic lead of unknown Pb207/Pb206 ratio. Practical numerical solutions for many of tho concordant age calculations are not currently available. However, the algebraic equivalents of these new graphical methods give equations which may be programmed for computing machines. For geologically probable parameters the equations of higher order have two positive real roots that rapidly converge on the exact concordant ages corrected for original radiogenic lead and for loss or gain of lead or uranium. Modifications of these general age equations expanded only to the second degree have been derived for use with desk calculators. These graphical and algebraic methods clearly suggest both the type and minimum number of samples necessary for adequate mathematical analysis of discordant lead isotope age data. This mathematical treatment also makes it clear t

A combined chemical, isotopic and microstructural study of pyrite from roll-front uranium deposits, Lake Eyre Basin, South Australia

NASA Astrophysics Data System (ADS)

Ingham, Edwina S.; Cook, Nigel J.; Cliff, John; Ciobanu, Cristiana L.; Huddleston, Adam

2014-01-01

The common sulfide mineral pyrite is abundant throughout sedimentary uranium systems at Pepegoona, Pepegoona West and Pannikan, Lake Eyre Basin, South Australia. Combined chemical, isotopic and microstructural analysis of pyrite indicates variation in fluid composition, sulfur source and precipitation conditions during a protracted mineralization event. The results show the significant role played by pyrite as a metal scavenger and monitor of fluid changes in low-temperature hydrothermal systems. In-situ micrometer-scale sulfur isotope analyses of pyrite demonstrated broad-scale isotopic heterogeneity (δ34S = -43.9 to +32.4‰VCDT), indicative of complex, multi-faceted pyrite evolution, and sulfur derived from more than a single source. Preserved textures support this assertion and indicate a genetic model involving more than one phase of pyrite formation. Authigenic pyrite underwent prolonged evolution and recrystallization, evidenced by a genetic relationship between archetypal framboidal aggregates and pyrite euhedra. Secondary hydrothermal pyrite commonly displays hyper-enrichment of several trace elements (Mn, Co, Ni, As, Se, Mo, Sb, W and Tl) in ore-bearing horizons. Hydrothermal fluids of magmatic and meteoric origins supplied metals to the system but the geochemical signature of pyrite suggests a dominantly granitic source and also the influence of mafic rock types. Irregular variation in δ34S, coupled with oscillatory trace element zonation in secondary pyrite, is interpreted in terms of continuous variations in fluid composition and cycles of diagenetic recrystallization. A late-stage oxidizing fluid may have mobilized selenium from pre-existing pyrite. Subsequent restoration of reduced conditions within the aquifer caused ongoing pyrite re-crystallization and precipitation of selenium as native selenium. These results provide the first qualitative constraints on the formation mechanisms of the uranium deposits at Beverley North. Insights into depositional conditions and sources of both sulfide and uranium mineralization and an improved understanding of pyrite geochemistry can also underpin an effective vector for uranium exploration at Beverley North and other sedimentary systems of the Lake Eyre Basin, as well as in comparable geological environments elsewhere. Average intensity of 32S signal in counts per second × 108.Drift corrected 34S/32S prior to IMF calibration.Two-sigma propagated uncertainty on individual measurements.

Underground gas storage in the Leyden lignite mine

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

Meddles, R.M.

1978-01-01

Underground gas storage in the Leyden lignite mine by Public Service Co. of Colorado was preceded by careful studies of mine records with respect to geologic conditions and investigation of the gas-sealing potential of the rocks surrounding the cavern. The water level in shaft No. 3 in Sept. 1958 was about 100 ft above the coal seam at that point. Wells were drilled into the mine up-dip (east) of the structurally highest point that a mine shaft intersected the coal seams, and gas was injected into the mine, using the mine water as a seal. At least the up-dip partmore » of the mine was gas-tight, and tests were expanded to the rest of the mine, which also proved to be gas-tight. All that remained to complete the preparation of the mine for permanent gas storage was sealing of the old mine shafts.« less

Evaluating nephrotoxicity of high-molecular-weight organic compounds in drinking water from lignite aquifers

USGS Publications Warehouse

Bunnell, J.E.; Tatu, C.A.; Lerch, H.E.; Orem, W.H.; Pavlovic, N.

2007-01-01

High-molecular-weight organic compounds such as humic acids and/or fulvic acids that are naturally mobilized from lignite beds into untreated drinking-water supplies were suggested as one possible cause of Balkan endemic nephropathy (BEN) and cancer of the renal pelvis. A lab investigation was undertaken in order to assess the nephrotoxic potential of such organic compounds using an in vitro tissue culture model. Because of the infeasibility of exposing kidney tissue to low concentrations of organics for years in the lab, tangential flow ultrafiltration was employed to hyperconcentrate samples suitable for discerning effects in the short time frames necessitated by tissue culture systems. Effects on HK-2 kidney cells were measured using two different cell proliferation assays (MTT and alamarBlue). Results demonstrated that exposure of kidney tissue to high-molecular-weight organics produced excess cell death or proliferation depending on concentration and duration of exposure. Copyright ?? Taylor & Francis Group, LLC.

Experimental Study of Hydrogasification of Lignite and Subbituminous Coal Chars

PubMed Central

Gil, Stanisław

2015-01-01

The experimental facility for pressure hydrogasification research was adapted to the pressure of 10 MPa and temperature of 1300 K, which ensured repeatability of results and hydrogen heating to the process temperature. A hydrogasification reaction of chars produced from two rank coals was investigated at temperatures up to 1173 K, pressures up to 8 MPa, and the gas flow rates of 0.5–5 dmn 3/min. Reactivity of the “Szczerców” lignite char was found to be slightly higher than that of the subbituminous “Janina” coal char produced under the same conditions. A high value of the char reactivity was observed to a certain carbon conversion degree, above which a sharp drop took place. It was shown that, to achieve proper carbon conversion, the hydrogasification reaction must proceed at a temperature above 1200 K. PMID:26065028

Structural analysis of geochemical samples by solid-state nuclear magnetic resonance spectrometry. Role of paramagnetic material

USGS Publications Warehouse

Vassallo, A.M.; Wilson, M.A.; Collin, P.J.; Oades, J.M.; Waters, A.G.; Malcolm, R.L.

1987-01-01

An examination of coals, coal tars, a fulvic acid, and soil fractions by solid-state 13C NMR spectrometry has demonstrated widely differing behavior regarding quantitative representation in the spectrum. Spin counting experiments on coal tars and the fulvic acid show that almost all the sample carbon is observed in both solution and solid-state NMR spectra. Similar experiments on two coals (a lignite and a bituminous coal) show that most (70-97%) of the carbon is observed; however, when the lignite is ion exchanged with 3% (w/w) Fe3+, the fraction of carbon observed drops to below 10%. In additional experiments signal intensity from soil samples is enhanced by a simple dithionite treatment. This is illustrated by 13C, 27Al, and 29Si solid-state NMR experiments on soil fractions. ?? 1987 American Chemical Society.

Stabilisation of bank slopes that are prone to liquefaction in ecologically sensitive areas.

PubMed

Nestler, P; Stoll, R D

2001-01-01

A consequence of lignite stripping in the Lusatia mining district (East Germany) is the backfilling of dumps that mainly consist of low-compacted fine and medium-grained sands. When the ground-water table, which had been lowered while stripping the coal, is rising again, these dumps might be affected by a settlement flow due to the liquefaction of soils. Common methods for stabilisation as, for instance, blasting or vibrator-jetting deep compaction, are not very useful in ecologically sensitive areas, where dumps have been afforested and embankment areas of residual lakes have developed into highly valuable biotopes. A new so-called air-impulse method in combination with directional horizontal drilling has been developed, which does not have a considerably negative impact on the vegetation during compaction. The experience gained during the first employment of this method at the lake "Katja", a residual lake of lignite stripping, is presented in this paper.

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

McKeigue, J.; Da Cunha, A.; Severino, D.

Turkey's growing power market has attracted investors and project developers for over a decade, yet their plans have been dashed by unexpected political or financial crises or, worse, obstructed by a lengthy bureaucratic approval process. Now, with a more transparent retail electricity market, government regulators and investors are bullish on Turkey. Is Turkey ready to turn the power on? This report closely examine Turkey's plans to create a power infrastructure capable of providing the reliable electricity supplies necessary for sustained economic growth. It was compiled with on-the-ground research and extensive interview with key industrial and political figures. Today, hard coalmore » and lignite account for 21% of Turkey's electricity generation and gas-fired plants account for 50%. The Alfin Elbistan-B lignite-fired plant has attracted criticism for its lack of desulfurization units and ash dam facilities that have tarnished the industry's image. A 1,100 MW hard-coal fired plant using supercritical technology is under construction. 9 figs., 1 tab.« less

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

Ali Sinag; Melike Sungur; Mustafa Gullu

This study describes the detailed hydrocarbon type characterization of the tar (liquid phase) obtained by copyrolysis of Mustafa Kemal Paa (M.K.P.) lignite (Turkey) and low density polyethylene (LDPE) and by pyrolysis of coal and LDPE individually. Various spectroscopic techniques (gas chromatography-mass spectroscopy (GC-MS), nuclear magnetic resonance spectroscopy ({sup 1}H NMR), Fourier transform infrared spectroscopy (FTIR), and gel permeation chromatography (GPC)) are used for characterization, and the effect of the experimental conditions (temperature, lignite:low density polyethylene (LDPE) ratio, and catalyst) on the hydrocarbon distributions is discussed. The results show that the tars obtained by copyrolysis have similar properties with commercial gasolinemore » (especially in the presence of Red mud). Red mud and bentonite used as catalysts make a positive effect on the production of olefins instead aromatics. Polyethylene acts as a hydrogenation medium for the coal product as revealed by FTIR results. 18 refs., 9 figs., 5 tabs.« less

Increasing arsenic concentrations in runoff from 12 small forested catchments (Czech Republic, Central Europe): patterns and controls.

PubMed

Novak, Martin; Erbanova, Lucie; Fottova, Daniela; Voldrichova, Petra; Prechova, Eva; Blaha, Vladimir; Veselovsky, Frantisek; Krachler, Michael

2010-08-01

The 40-year long period of heavy industrialization in Central Europe (1950-1990) was accompanied by burning of arsenic-rich lignite in thermal power plants, and accumulation of anthropogenic arsenic in forest soils. There are fears that retreating acidification may lead to arsenic mobilization into drinking water, caused by competitive ligand exchange. We present monthly arsenic concentrations in surface runoff from 12 headwater catchments in the Czech Republic for a period of 13 years (1996-2008). The studied area was characterized by a north-south gradient of decreasing pollution. Acidification, caused mainly by SOx and NOx emissions from power plants, has been retreating since 1987. Between 1996 and 2003, maximum arsenic concentrations in runoff did not change, and were < 1 ppb in the rural south and < 2 ppb in the industrial north. During the subsequent two years, 2004-2005, maximum arsenic concentrations in runoff increased, reaching 60% of the drinking water limit (10 ppb). Starting in 2006, maximum arsenic concentrations returned to lower values at most sites. We discuss three possible causes of the recent arsenic concentration maximum in runoff. We rule out retreating acidification and a pulse of high industrial emission rates as possible controls. The pH of runoff has not changed since 1996, and is still too low (<6.5) at most sites for an As-OH(-) ligand exchange to become significant. Elevated arsenic concentrations in runoff in 2004-2005 may reflect climate change through changing hydrological conditions at some, but not all sites. Dry conditions may result in elevated production of DOC and sulfur oxidation in the soil. Subsequent wet conditions may be accompanied by acidification leading to faster dissolution of arsenic-bearing sulfides, dissolution of arsenic-bearing Fe-oxyhydroxides, and elevated transport of arsenic sorbed on organic matter. Anaerobic domains exist in normally well-aerated upland soils for hours-to-days following precipitation events. 2010 Elsevier B.V. All rights reserved.

Age model for a continuous, ca 250-ka Quaternary lacustrine record from Bear Lake, Utah-Idaho

USGS Publications Warehouse

Colman, Steven M.; Kaufman, D.S.; Bright, Jordon; Heil, C.; King, J.W.; Dean, W.E.; Rosenbaum, J.G.; Forester, R.M.; Bischoff, J.L.; Perkins, Marie; McGeehin, J.P.

2006-01-01

The Quaternary sediments sampled by continuous 120-m-long drill cores from Bear Lake (Utah-Idaho) comprise one of the longest lacustrine sequences recovered from an extant lake. The cores serve as a good case study for the construction of an age model for sequences that extend beyond the range of radiocarbon dating. From a variety of potential age indicators, we selected a combination of radiocarbon ages, one magnetic excursion (correlated to a standard sequence), and a single Uranium-series age to develop an initial data set. The reliability of the excursion and U-series data require consideration of their position with respect to sediments of inferred interglacial character, but not direct correlation with other paleoclimate records. Data omitted from the age model include amino acid age estimates, which have a large amount of scatter, and tephrochronology correlations, which have relatively large uncertainties. Because the initial data set was restricted to the upper half of the BL00-1 core, we inferred additional ages by direct correlation to the independently dated paleoclimate record from Devils Hole. We developed an age model for the entire core using statistical methods that consider both the uncertainties of the original data and that of the curve-fitting process, with a combination of our initial data set and the climate correlations as control points. This age model represents our best estimate of the chronology of deposition in Bear Lake. Because the age model contains assumptions about the correlation of Bear Lake to other climate records, the model cannot be used to address some paleoclimate questions, such as phase relationships with other areas.

Heavy minerals and sedimentary organic matter in Pleistocene and Cretaceous sediments on Long Island, New York, with emphasis on pyrite and marcasite in the Magothy aquifer

USGS Publications Warehouse

Brown, Craig J.; Rakovan, John; Schoonen, Martin A.A.

2000-01-01

Abundance and distribution of iron-bearing and other heavy minerals in sediments of Long Island, N.Y., were examined to identify sources and sinks of dissolved iron and other ground-water constituents along a deep flow path from the ground-water divide to the southern shore along the Nassau-Suffolk County border. The occurrence and reactivity of many iron-bearing minerals in the aquifer system are affected by terminal electron-accepting processes, which are a function of depth below land surface, distance from the ground-water divide, and organic-matter content of the sediment. The lateral distribution of heavy minerals within lithologic sediments is not uniform throughout Long Island, or even along the 30-kilometer study section at the Nassau-Suffolk County border. Mineralogy and mineral abundance in Pleistocene units differ from those in Cretaceous sediments, and some of the trends vary with depth as well as from north to south. Major heavy minerals in the Cretaceous sediments at the study sites include pyrite, marcasite, muscovite, leucoxene, ilmenite, rutile, staurolite, chloritoid, and aluminosilicates (Al2SiO5); those in the overlying Pleistocene deposits at one site include iron oxides, leucoxene, zircon, garnet, ilmenite, aluminosilicates, and hornblende. Pyrite, marcasite, garnet, hornblende, and tourmaline were found locally in the Cretaceous sediments. Pyrite and marcasite were detected less frequently in borehole samples from near the ground-water divide, where the ground water is generally oxic, than in those from near the southern shore of Long Island, but were found in sulfate- reducing zones throughout the Magothy aquifer. Glauconite was present in Cretaceous and Pleistocene deposits, but only in the marine or transitional units. The most abundant and potentially reactive of the iron-bearing minerals found were iron (hydr)oxides, leucoxene, glauconite, chlorite, pyrite, and marcasite. The presence and morphology of pyrite and marcasite can be indicative of the microbial and geochemical environments. Pyrite generally was found in association with lignite or as interstitial cement. Marcasite was found as interstitial cement and is associated with the oxidation of iron-sulfide minerals upgradient. Pyrite crystals were octahedral, cubic, cubo-octahedral, and framboidal, and many samples showed more than one generation of crystal growth. Marcasite cement, which consisted of platey crystals in most samples, probably forms only under nonmarine conditions.

Evaluation of Thermal Evolution Profiles and Estimation of Kinetic Parameters for Pyrolysis of Coal/Corn Stover Blends Using Thermogravimetric Analysis

DOE PAGES

Bhagavatula, Abhijit; Huffman, Gerald; Shah, Naresh; ...

2014-01-01

The thermal evolution profiles and kinetic parameters for the pyrolysis of two Montana coals (DECS-38 subbituminous coal and DECS-25 lignite coal), one biomass sample (corn stover), and their blends (10%, 20%, and 30% by weight of corn stover) have been investigated at a heating rate of 5°C/min in an inert nitrogen atmosphere, using thermogravimetric analysis. The thermal evolution profiles of subbituminous coal and lignite coal display only one major peak over a wide temperature distribution, ~152–814°C and ~175–818°C, respectively, whereas the thermal decomposition profile for corn stover falls in a much narrower band than that of the coals, ~226–608°C. Themore » nonlinearity in the evolution of volatile matter with increasing percentage of corn stover in the blends verifies the possibility of synergistic behavior in the blends with subbituminous coal where deviations from the predicted yield ranging between 2% and 7% were observed whereas very little deviations (1%–3%) from predicted yield were observed in blends with lignite indicating no significant interactions with corn stover. In addition, a single first-order reaction model using the Coats-Redfern approximation was utilized to predict the kinetic parameters of the pyrolysis reaction. The kinetic analysis indicated that each thermal evolution profile may be represented as a single first-order reaction. Three temperature regimes were identified for each of the coals while corn stover and the blends were analyzed using two and four temperature regimes, respectively.« less

Reservoir characteristics of two minter oil sands based on continuous core, E-logs, and geochemical data: Bee Brake field, East-Central Louisiana

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

Echols, J.B.; Goddard, D.A.; Bouma, A.

The Bee Brake field area, located in township 4N/6E and 4N/7E in Concordia Parish, has been one of the more prolific oil-producing areas in east-central Louisiana. Production decline in various fields, however, has sparked interest in the economic feasibility of locating and producing the remaining bypassed oil in the lower Wilcox. For this purpose, the Angelina BBF No. 1 well was drilled, and a 500-ft conventional core and a complete suite of state-of-the-are wireline logs were recovered. Production tests were run on the Minter interval of interest. The 16-ft Minter interval (6742-6758 ft depth), bounded at its top and basemore » by lignite seams, consists of an upper 4-ft oil sand (Bee Brake) and a lower 3-ft oil sand (Angelina). The oil sands are separated by approximately 5 ft of thinly laminated silty shale and 4 ft of very fine-grained silty sandstone. Detailed sedimentologic and petrographic descriptions of the Minter interval provide accurate facies determinations of this lower delta-plain sequence. Petrophysical evaluation, combining core plug and modern electric-log data show differences between reservoir quality of the Bee Brake and Angelina sands. This data will also be useful for correlating and interpolating old electric logs. Organic geochemistry of the oil, lignites, and shales provides insight as to the source of the Minter oils and the sourcing potential of the lignites.« less

Evaluation of Thermal Evolution Profiles and Estimation of Kinetic Parameters for Pyrolysis of Coal/Corn Stover Blends Using Thermogravimetric Analysis

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

Bhagavatula, Abhijit; Huffman, Gerald; Shah, Naresh

The thermal evolution profiles and kinetic parameters for the pyrolysis of two Montana coals (DECS-38 subbituminous coal and DECS-25 lignite coal), one biomass sample (corn stover), and their blends (10%, 20%, and 30% by weight of corn stover) have been investigated at a heating rate of 5°C/min in an inert nitrogen atmosphere, using thermogravimetric analysis. The thermal evolution profiles of subbituminous coal and lignite coal display only one major peak over a wide temperature distribution, ~152–814°C and ~175–818°C, respectively, whereas the thermal decomposition profile for corn stover falls in a much narrower band than that of the coals, ~226–608°C. Themore » nonlinearity in the evolution of volatile matter with increasing percentage of corn stover in the blends verifies the possibility of synergistic behavior in the blends with subbituminous coal where deviations from the predicted yield ranging between 2% and 7% were observed whereas very little deviations (1%–3%) from predicted yield were observed in blends with lignite indicating no significant interactions with corn stover. In addition, a single first-order reaction model using the Coats-Redfern approximation was utilized to predict the kinetic parameters of the pyrolysis reaction. The kinetic analysis indicated that each thermal evolution profile may be represented as a single first-order reaction. Three temperature regimes were identified for each of the coals while corn stover and the blends were analyzed using two and four temperature regimes, respectively.« less

Characterizing thermogenic coalbed gas from Polish coals of different ranks by hydrous pyrolysis

USGS Publications Warehouse

Kotarba, M.J.; Lewan, M.D.

2004-01-01

To provide a better characterization of origin and volume of thermogenic gas generation from coals, hydrous pyrolysis experiments were conducted at 360??C for 72 h on Polish coals ranging in rank from lignite (0.3% R r) to semi-anthracite (2.0% Rr). Under these conditions, the lignites attained a medium-volatile bituminous rank (1.5% Rr), high-volatile bituminous coals attained a low-volatile bituminous rank (1.7% Rr), and the semi-anthracite obtained an anthracite rank (4.0% R r). Hydrous pyrolysis of a coal, irrespective of rank, provides a diagnostic ??13C value for its thermogenic hydrocarbon gases. This value can be used quantitatively to interpret mixing of indigenous thermogenic gas with microbial methane or exogenous thermogenic gas from other sources. Thermogenic methane quantities range from 20 dm3/kg of lignite (0.3% Rr) to 0.35 dm3/kg of semi-anthracite (2.0% Rr). At a vitrinite reflectance of 1.7% Rr, approximately 75% of the maximum potential for a coal to generate thermogenic methane has been expended. At a vitrinite reflectance of 1.7% Rr, more than 90% of the maximum potential for a coal to generate CO2 has been expended. Assuming that these quantities of generated CO2 remain associated with a sourcing coal bed as uplift or erosion provide conditions conducive for microbial methanogenesis, the resulting quantities of microbial methane generated by complete CO2 reduction can exceed the quantities of thermogenic methane generated from the same coal bed by a factor of 2-5. ?? 2004 Elsevier Ltd. All rights reserved.

Regulation of coal polymer degradation by fungi. Tenth Quartery report, October 1996--December 1996

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

Irvine, R.L.; Bumpus, J.A.

1997-01-28

It has long been known that low rank coal such as leonardite can be solubilized by strong base (>pH 12). Recent discoveries have also shown that leonardite is solubilized by Lewis bases at considerably lower pH values and by fungi that secrete certain Lewis bases (i.e., oxalate ion). During the current reporting period we have studied the ability of a strong base (sodium hydroxide, pH 12), and two fungi, Phanerochaete chrysosporium and Trametes versicolor, to solubilize Argonne Premium Coals. In general, Argonne Premium Coals were relatively resistant to base mediated solubilization. However, when these coals were preoxidized (150{degrees}C for sevenmore » days), substantial amounts of several coals were solubilized. Most affected were the Lewiston-Stockton bituminous coal, the Beulah-Zap lignite, the Wyodak-Anderson subbituminous coal and the Blind Canyon bituminous coal. Argonne Premium Coals were previously shown by us to be relatively resistant to solubilization by sodium oxalate. When preoxidized coals were treated with sodium oxalate, only the Beulah-Zap lignite was substantially solubilized. Although very small amounts of the other preoxidized coals were solubilized by treatment with oxalate, the small amount of solubilization that did take place was generally increased relative to that observed for coals that were not preoxidized. None of the Argonne Premium Coals were solubilized by P. chrysosporium or T. versicolor. Of considerable interest, however, is the observation that P. chrysosporium and T. versicolor mediated extensive solubilization of Lewiston-Stockton bituminous coal, the Beulah-Zap lignite and the Wyodak-Anderson subbituminous coal.« less

Utilization of lignite power generation residues for the production of lightweight aggregates.

PubMed

Anagnostopoulos, Iason M; Stivanakis, Victor E

2009-04-15

A novel process is proposed for the utilization of lignite combustion solid residues in the production of inflammable lightweight aggregates (LWA). The process consists of two stages, pelletization and sintering, and carbon contained in BA was used as the process fuel. The main residues bottom ash (BA) and fly ash (FA) from Megalopolis power plant were characterized, mixed in different proportions and treated through pelletization and sintering process. Sintering benefits from combustion of BA carbon content and the product is a hardened porous cake. The energy required for achievement of high temperatures, in the range of 1250 degrees C, was offered by carbon combustion and CO(2) evolution is responsible for porous structure formation. Selected physical properties of sintered material relevant to use as lightweight aggregates were determined, including bulk density, porosity and water absorption. Bulk density varies from 0.83 to 0.91 g/cm(3), porosity varies from 60% to 64% and water absorption varies from 66% to 80%. LWA formed is used for the production of lightweight aggregate concrete (LWAC). Thermal conductivity coefficient varies from 0.25 to 0.37 W/mK (lower than maximum limit 0.43 W/mK) and compressive strength varies from 19 to 23 MPa (higher than minimum limit 17 MPa). The results indicate that sintering of lignite combustion residues is an efficient method of utilization of carbon containing BA and production of LWA for structural and insulating purposes. Carbon content of BA is a key factor in LWA production. Finally, this research work comprises the first proposed application for utilization of BA in Greece.

Pipeline transportation of upgraded Yugoslavian lignite fuels

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

Ljubicic, B.; Anderson, C.; Bukurov, Z.

1993-12-31

Hydraulic transport and handling procedures for coal are not widely used, but when practiced, they result in a technically and economically successful operation. Potentially the most attractive way to utilize lignitic coals for power generation would be to combine hydraulic mining techniques with aqueous ash removal, hydrothermal processing, solids concentration, and coal-water fuel (CWF) combustion. Technical and economic assessment of this operation is being implemented within the Yugoslavian-American Scientific Technical Cooperation Agreement. The Energy and Environmental Research Center (EERC), Grand Forks, North Dakota, with support from the U.S. Department of Energy, has entered into a jointly sponsored research project withmore » Electric Power of Serbia (EPS), Belgrade, Yugoslavia, to investigate the application of the nonevaporative hydrothermal drying procedure, commonly called hot-water drying (HWD), developed at the EERC, to the lignite from the Kovin deposit. Advances in hydrothermal treatment of low-rank coals (LRCs) at the EERC have enabled cheaper, more reactive LRCs to be used in coal-water fuels (CWFs). HWD is a high-temperature, nonevaporative drying technique carried out at high pressure in water that permanently alters the structure of LRC. It solves the stability problems by producing a safe, easily transported, liquid fuel that can be handled and used like oil. For continued or increased success, it is necessary to evaluate carefully all aspects of slurry technology that permit further optimization. This paper discusses some aspects of low-rank coal hydraulic transport combined with hydrothermal treatment as an alternative energy solution toward less oil dependence in Yugoslavia.« less

Mass Transport of Condensed Species in Aerodynamic Fallout Glass from a Near-Surface Nuclear Test

NASA Astrophysics Data System (ADS)

Weisz, David Gabriel

In a near-surface nuclear explosion, vaporized device materials are incorporated into molten soil and other carrier materials, forming glassy fallout upon quenching. Mechanisms by which device materials mix with carrier materials have been proposed, however, the specific mechanisms and physical conditions by which soil and other carrier materials interact in the fireball, as well as the subsequent incorporation of device materials with carrier materials, are not well constrained. A surface deposition layer was observed preserved at interfaces where two aerodynamic fallout glasses agglomerated and fused. Eleven such boundaries were studied using spatially resolved analyses to better understand the vaporization and condensation behavior of species in the fireball. Using nano-scale secondary ion mass spectrometry (NanoSIMS), we identified higher concentrations of uranium from the device in 7 of the interface layers, as well as isotopic enrichment (>75% 235U) in 9 of the interface layers. Major element analysis of the interfaces revealed the deposition layer to be chemically enriched in Fe-, Ca- and Na-bearing species and depleted in Ti- and Al-bearing species. The concentration profiles of the enriched species at the interface are characteristic of diffusion. Three of the uranium concentration profiles were fit with a modified Gaussian function, representative of 1-D diffusion from a planar source, to determine time and temperature parameters of mass transport. By using a historical model of fireball temperature to simulate the cooling rate at the interface, the temperature of deposition was estimated to be 2200 K, with 1? uncertainties in excess of 140 K. The presence of Na-species in the layers at this estimated temperature of deposition is indicative of an oxygen rich fireball. The notable depletion of Al-species, a refractory oxide that is highly abundant in the soil, together with the enrichment of Ca-, Fe-, and 235U-species, suggests an anthropogenic source of the enriched species, together with a continuous chemical fractionation process as these species condensed.

Selected annotated bibliography of the geology of uraniferous and radioactive native bituminous substances, exclusive of coals, in the United States

USGS Publications Warehouse

Jones, Harriet Nell

1956-01-01

Native bituminous substances are divided into two groups, 1) bitumens and, 2) pyrobitumens. Bitumens are composed principally of hydrocarbons substantially free from oxygenated bodies, are fusible, and are soluble in carbon disulfide. Native bitumens occur in liquid and solid forms. The native liquid bitumens include all petroleums or crude oils. Native solid bitumens include native waxes such as ozocerite, asphalts or petroleum tars, and asphaltites such as gilsonite and grahamite. Pyrobitumens are composed principally of hydrocarbons which may contain oxygenated bodies. They are infusible and are insoluble, or nearly insoluble, in carbon disulfide. Native pyrobitumens are divided into an oxygen-containing group including peats, lignites, and coals, and an essentially oxygen-free, asphaltic group including such substances as wurtzilite, albertite, impsonite, and ingramite. Thucholites, which are carbonaceous substances that may contain uranium, thorium, and rare earths, commonly are considered to be pyrobitumens. Their compositions are variable and may fall into either the oxygen-containing or oxygen-free group. All varieties of native bituminous substances may be associated with mineral matter. The nomenclature of bitumens and pyrobitumens is used very loosely in the literature. This circumstance arises from the difficulty in recognizing many of these substances by visual examination, and because many of them can be identified accurately only by chemical methods. Inasmuch as some of the chemical procedures are time-consuming and satisfactory analytical methods have not been devised for all these substances, geologists generally have not obtained precise identifications but rather have used names that appeared most appropriate to the circumstances. It is expected that future research will show many substances called "asphaltite," "thucholite," etc., to be incorrectly identified. The nomenclature used by the authors of the various references of this bibliography is followed without deviation or further discussion. The stratigraphic nomenclature also is that used by the authors. In this bibliography emphasis is placed on reports dealing with the uranium contents and radioactivity of native bituminous substances rather than on mineralogical and chemical studies of these substances. The distribution of the substances described in the references is shown on the accompanying map. The indicated presence of these substances does not infer that they contain sufficient radioactive elements to constitute ores.

SHIPMENT OF TWO DOE-STD-3013 CONTAINERS IN A 9977 TYPE B PACKAGE

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

Abramczyk, G.; Bellamy, S.; Loftin, B.

2011-06-06

The 9977 is a certified Type B Packaging authorized to ship uranium and plutonium in metal and oxide forms. Historically, the standard container for these materials has been the DOE-STD-3013 which was specifically designed for the long term storage of plutonium bearing materials. The Department of Energy has used the 9975 Packaging containing a single 3013 container for the transportation and storage of these materials. In order to reduce container, shipping, and storage costs, the 9977 Packaging is being certified for transportation and storage of two 3013 containers. The challenges and risks of this content and the 9977s ability tomore » meet the Code of Federal Regulations for the transport of these materials are presented.« less

Calculation of the temperature in the container unit with a modified design for the production of {sup 99}Mo at the VVR-Ts research reactor facility (IVV.10M)

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

Kazantsev, A. A., E-mail: kazantsevanatoly@gmail.com; Sergeev, V. V.; Kochnov, O. Yu.

The temperature regime is calculated for two different designs of containers with uranium-bearing material for the upgraded VVR-Ts research reactor facility (IVV.10M). The containers are to be used in the production of {sup 99}Mo. It is demonstrated that the modification of the container design leads to a considerable temperature reduction and an increase in the near-wall boiling margin and allows one to raise the amount of material loaded into the container. The calculations were conducted using the international thermohydraulic contour code TRAC intended to analyze the technical safety of water-cooled nuclear power units.

Evidence for the timing and duration of the last interglacial period from high-precision uranium-series ages of corals on tectonically stable coastlines

USGS Publications Warehouse

Muhs, D.R.

2002-01-01

The last interglacial period has a timing and duration that can be estimated from U-series dating of emergent, coral-bearing deposits on tectonically stable coastlines. High-precision dating from Bermuda, the Bahamas, Hawaii, and Australia suggests that the last interglacial period had a sea level at least as high as present from ???128,000 to 116,000 yr B.P. Sea level reached a near-present level more quickly after the close of the penultimate glacial period than at the close of the last glacial period and the duration of high sea level is longer than that implied by the deep-sea record. ?? 2002 University of Washington.

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

Chambers, Doug; Wiatzka, Gerd; Brown, Steve

This paper provides the life story of Canada's original radium/uranium mine. In addition to the history of operations, it discusses the unique and successful approach used to identify the key issues and concerns associated with the former radium, uranium and silver mining property and the activities undertaken to define the remedial actions and subsequent remedial plan. The Port Radium Mine site, situated approximately 275 km north of Yellowknife on the east shore of Great Bear Lake, Northwest Territories, was discovered in 1930 and underground mining began in 1932. The mine operated almost continuously from 1932 to 1982, initially for recoverymore » of radium, then uranium and finally, for recovery of silver. Tailings production totaled an estimated 900,000 tons and 800,000 tons from uranium and silver processing operations respectively. In the early days of mining, Port Radium miners were exposed to radon and associated decay product levels (in Working Level Months of exposure - WLM) hundreds of times greater than modern standards. The experience of the Port Radium miners provides important contribution to understanding the risks from radon. While the uranium mine was originally decommissioned in the early 1960's, to the standards of the day, the community of Deline (formerly Fort Franklin) had concerns about residual contamination at the mine site and the potential effects arising from use of traditional lands. The Deline people were also concerned about the possible risks to Deline Dene arising from their work as ore carriers. In the late 1990's, the community of Deline brought these concerns to national attention and consequently, the Government of Canada and the community of Deline agreed to move forward in a collaborative manner to address these concerns. The approach agreed to was to establish the Canada-Deline Uranium Table (CDUT) to provide a joint process by which the people of Deline could have their concerns expressed and addressed. A great deal of work was done through the CDUT, including efforts to assess site environment and safety issues in the context of modern reclamation standards. In addition to the environmental and remediation studies, an assessment of historic exposures of Deline ore carriers to radiation and a follow-up epidemiological feasibility study were performed. SENES Consultants Limited (SENES) carried out the dose reconstruction for the Port Radium miners in the 1990's, was the environmental consultant to the CDUT from 2000 to 2005, developed the Remedial Action Plan (RAP), engineering plans and specifications for decommissioning the Port Radium mine and vicinity sites in 2005/6, supervised the remedial works in 2007 and carried out the long term post closure monitoring from 2008 to 2012. Our firsthand experience from working cooperatively with the CDUT provides insights into effective decommissioning of historic contaminated sites. (authors)« less

Porous metal oxide microspheres from ion exchange resin

NASA Astrophysics Data System (ADS)

Picart, S.; Parant, P.; Caisso, M.; Remy, E.; Mokhtari, H.; Jobelin, I.; Bayle, J. P.; Martin, C. L.; Blanchart, P.; Ayral, A.; Delahaye, T.

2015-07-01

This study is devoted to the synthesis and the characterization of porous metal oxide microsphere from metal loaded ion exchange resin. Their application concerns the fabrication of uranium-americium oxide pellets using the powder-free process called Calcined Resin Microsphere Pelletization (CRMP). Those mixed oxide ceramics are one of the materials envisaged for americium transmutation in sodium fast neutron reactors. The advantage of such microsphere precursor compared to classical oxide powder is the diminution of the risk of fine dissemination which can be critical for the handling of highly radioactive powders such as americium based oxides and the improvement of flowability for the filling of compaction chamber. Those millimetric oxide microspheres incorporating uranium and americium were synthesized and characterizations showed a very porous microstructure very brittle in nature which occurred to be adapted to shaping by compaction. Studies allowed to determine an optimal heat treatment with calcination temperature comprised between 700-800 °C and temperature rate lower than 2 °C/min. Oxide Precursors were die-pressed into pellets and then sintered under air to form regular ceramic pellets of 95% of theoretical density (TD) and of homogeneous microstructure. This study validated thus the scientific feasibility of the CRMP process to prepare bearing americium target in a powder free manner.

A geochronologic framework for the Ziegler Reservoir fossil site, Snowmass Village, Colorado

USGS Publications Warehouse

Mahan, Shannon; Gray, Harrison J.; Pigati, Jeffrey S.; Wilson, Jim; Lifton, Nathaniel A.; Paces, James B.; Blaauw, Maarten

2014-01-01

The Ziegler Reservoir fossil site near Snowmass Village, Colorado, provides a unique opportunity to reconstruct high-altitude paleoenvironmental conditions in the Rocky Mountains during the last interglacial period. We used four different techniques to establish a chronological framework for the site. Radiocarbon dating of lake organics, bone collagen, and shell carbonate, and in situ cosmogenic 10Be and 26Al ages on a boulder on the crest of a moraine that impounded the lake suggest that the ages of the sediments that hosted the fossils are between ~ 140 ka and > 45 ka. Uranium-series ages of vertebrate remains generally fall within these bounds, but extremely low uranium concentrations and evidence of open-system behavior limit their utility. Optically stimulated luminescence (OSL) ages (n = 18) obtained from fine-grained quartz maintain stratigraphic order, were replicable, and provide reliable ages for the lake sediments. Analysis of the equivalent dose (DE) dispersion of the OSL samples showed that the sediments were fully bleached prior to deposition and low scatter suggests that eolian processes were likely the dominant transport mechanism for fine-grained sediments into the lake. The resulting ages show that the fossil-bearing sediments span the latest part of marine isotope stage (MIS) 6, all of MIS 5 and MIS 4, and the earliest part of MIS 3.

The role of the thermal convection of fluids in the formation of unconformity-type uranium deposits: the Athabasca Basin, Canada

NASA Astrophysics Data System (ADS)

Pek, A. A.; Malkovsky, V. I.

2017-05-01

In the global production of uranium, 18% belong to the unconformity-type Canadian deposits localized in the Athabasca Basin. These deposits, which are unique in terms of their ore quality, were primarily studied by Canadian and French scientists. They have elaborated the diagenetic-hydrothermal hypothesis of ore formation, which suggests that (1) the deposits were formed within a sedimentary basin near an unconformity surface dividing the folded Archean-Proterozoic metamorphic basement and a gently dipping sedimentary cover, which is not affected by metamorphism; (2) the spatial accommodation of the deposits is controlled by the rejuvenated faults in the basement at their exit into the overlying sedimentary sequence; the ore bodies are localized above and below the unconformity surface; (3) the occurrence of graphite-bearing rocks is an important factor in controlling the local structural mineralization; (4) the ore bodies are the products of uranium precipitation on a reducing barrier. The mechanism that drives the circulation of ore-forming hydrothermal solutions has remained one of the main unclear questions in the general genetic concept. The ore was deposited above the surface of the unconformity due to the upflow discharge of the solution from the fault zones into the overlying conglomerate and sandstone. The ore formation below this surface is a result of the downflow migration of the solutions along the fault zones from sandstone into the basement rocks. A thermal convective system with the conjugated convection cells in the basement and sedimentary fill of the basin may be a possible explanation of why the hydrotherms circulate in the opposite directions. The results of our computations in the model setting of the free thermal convection of fluids are consistent with the conceptual reasoning about the conditions of the formation of unique uranium deposits in the Athabasca Basin. The calculated rates of the focused solution circulation through the fault zones in the upflow and downflow branches of a convection cell allow us to evaluate the time of ore formation up to the first hundreds of thousands years.

Pyrochlore-rich titanate ceramics for the immobilization of plutonium: redox effects on phase equilibria in cerium- and thorium- substituted analogs

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

Ryerson, F J; Ebbinghaus, B

2000-05-25

Three compositions representing plutonium-free analogs of a proposed Ca-Ti-Gd-Hf-U-PU oxide ceramic for the immobilization of plutonium were equilibrated at 1 atm, 1350 C over a range of oxygen fugacities between air and that equivalent to the iron-wuestite buffer. The cerium analog replaces Pu on a mole-per-mole basic with Ce; the thorium analog replaces Pu with Th. A third material has 10 wt% Al{sub 2}O{sub 3} added to the cerium analog to encourage the formation of a Hf-analog of, CaHfTi{sub 2}O{sub 7}, zirconolite, which is referred to as hafnolite. The predominant phase produced in each formulation under all conditions is pyrochlore,more » A{sub 2}T{sub 2}O{sub 7}, where the T site is filled by Ti, and Ca, the lanthanides, Hf, U and Pu are accommodated on the A-site. Other lanthanide and uranium-bearing phases encountered include brannerite (UTi{sub 2}O{sub 6}), hafnolite (CaHfTi{sub 2}O{sub 7}), perovskite (CaTiO{sub 3}) and a calcium-lanthanide aluminotitanate with nominal stoichiometry (Ca,Ln)Ti{sub 2}Al{sub 9}O{sub 19}, where Ln is a lanthanide. The phase compositions show progressive shifts with decreasing oxygen fugacity. All of the phases observed have previously been identified in titanate-based high-level radioactive waste ceramics and demonstrate the flexibility of these ceramics to variations in processing parameters. The main variation is an increase in the uranium concentrations of pyrochlore and brannerite which must be accommodated by variations in modal abundance. Pyrochlore compositions are consistent with existing spectroscopic data suggesting that uranium is predominantly pentavalent in samples synthesized in air. A simple model based on ideal stoichiometry suggests the U{sup +4}/{Sigma}U varies linearly with log fO{sub 2} and that all of the uranium is quadravalent at the iron-wuestite buffer.« less

Diffusive parameters of tritiated water and uranium in chalk

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

Descostes, M.; UMR 8587 CEA, Universite d'Evry, CNRS,; Pili, E.

2012-07-15

The Cretaceous Chalk of North-western Europe exhibits a double porosity (matrix and fracture) providing pathways for both slow and rapid flow of water. The present study aims at understanding and predicting the contaminant transfer properties through a significant section of this formation, with a particular emphasis on diffusion. This requires to study the nature of porosity and to perform diffusion experiments in representative samples using uranium and tritiated water (HTO), respectively taken as a reactive tracer and an inert one. The diffusive parameters, i.e. the accessible porosity and the effective diffusion coefficient were determined. Additional information was obtained with mercurymore » porosimetry, gravimetric water content, textural and mineralogical characterization. The diffusion tests performed with HTO appear to be the best method to measure the total accessible porosity in any type of porous media, especially those having large pore size distributions. Our study demonstrates that classical gravimetric water content measurements are not sensitive to the reduction in pore size as opposed to HTO diffusion tests because capillary water is not extracted by conventional gravimetric method but can still be probed by diffusion experiments. We found effective diffusion coefficients D{sub e}(U(VI)) near 4 x 10{sup -10} m{sup 2}s{sup -1}). The slower migration of U(VI) compared to HTO indicates sorption, with R{sub d}(U(VI)) from 100 to 360 mL g{sup -1}. These values are one order of magnitude larger than other determinations of the U(VI) sorption coefficient because only the matrix porosity is concerned here. The migration of U(VI) in chalk is only limited by sorption on ancillary Fe-Pb-bearing minerals. Transport of HTO and U(VI) is independent of the porosity distribution. Uranium diffusion in the chalk matrix porosity is fast enough to allow the total invasion of the pore space within characteristic time scales of the order of 1000 years. This results in a partitioning of uranium velocities in fracture flow and matrix flow proportionally to the respective fracture and matrix porosities. (authors)« less

Organic geochemical studies of the transformation of gymnospermous xylem during peatification and coalification to subbituminous coal

USGS Publications Warehouse

Hatcher, P.G.; Lerch, H. E.; Verheyen, T.V.

1990-01-01

It is generally recognized that xylem from trees that are buried in peat swamps is transformed first to huminite macerals in brown coal and then to vitrinite macerals in bituminous coal by processes collectively known as coalification. In order to understand the chemical nature of coalification of xylem and the chemical structures that eventually evolve in coal, we examined a series of gymnospermous xylem samples coalified to varying degrees. The samples included modern fresh xylem, modern degraded xylem in peat, and xylem coalified to ranks of brown coal (lignite B), lignite A, and subbituminous coal. The organic geochemical methods used in this study included solid-state 13C nuclear magnetic resonance (NMR) and pyrolysis/gas chromatography/mass spectrometry. The NMR method provided average compositional information, and the pyrolysis provided detailed molecular information. Although the samples examined include different plants of different geologic ages, they all share a common feature in that they are gymnospermous and presumably have or had a similar kind of lignin. The data obtained in this study provide enough details to allow delineation of specific coalification pathway for the xylem is microbial degradation in peat (peatification), leading to selective removal of cellulosic components. These components constitute a large fraction of the total mass of xylem, usually greater than 50%. Although cellulosic components can survive degradation under certain conditions, their loss during microbial degradation is the rule rather than exception during peatification. As these components of xylem are degraded and lost, lignin, another major component of xylem, is selectively enriched because it is more resistant to microbial degradation than the cellulosic components. Thus, lignin survives peatification in a practically unaltered state and becomes the major precursor of coalified xylem. During its transformation to brown coal and lignite A, lignin in xylem is altered by two important processes. The first involves loss of methoxyl groups, primarily by demethylation (Fig. 1A). The end products of demethylation are catechol-like structures as shown below in Figure 1B. The second transformation process involves increased cross-linking of the aromatic rings. This cross-linking induces increased carbon substitution of the aromatic rings such that the lignin-derived structures become more highly condensed. During its conversion to coalified xylem in subbituminous coal, lignitic xylem, composed primarily of condensed catechol-like structures, is transformed to a macromolecular material primarily composed of phenol-like structures. The catechol-like structures of lignitic xylem loose a hydroxyl group, which is replaced by a hydrogen to form the phenol-like structure as shown in the example in Figure 1B. The pyrolysis data provided only a few clues as to the fate of the C3-side chain of lignin during coalification. However, the NMR data suggest that this side chain is altered, probably by loss of the hydroxyl groups that are attached in modern lignin. Interference in the NMR analysis by aliphatic components of wood, such as resins, precludes definitive determinations of the fate of the C3-side chain during coalification. ?? 1990.

Testing the potential of bacterial branched tetraether membrane lipids as temperature proxy in peat and immature coal deposits

NASA Astrophysics Data System (ADS)

Weijers, J. W. H.; Steinmann, P.; Hopmans, E. C.; Basiliko, N.; Finkelstein, S. A.; Johnson, K. R.; Schouten, S.; Sinninghe Damsté, J. S.

2012-04-01

Branched glycerol dialkyl glycerol tetraether (brGDGT) membrane lipids occur ubiquitously in peat and soil. In soil, the degree of methylation and cyclisation of branched tetraethers (MBT index and CBT ratio, respectively) has shown to relate to both soil pH and annual mean air temperature (MAT). Using this relation, past annual MATs can be reconstructed by analysing brGDGTs in marine sediment records near large river outflows. More recently, the potential of this MBT/CBT proxy is also being explored in lakes. Despite being more abundant in peat than soils, however, the utility of the proxy has not yet been fully explored in peat records. Present day peat records generally extent back to the early Holocene, but if the MBT/CBT proxy were shown to be applicable in peat deposits, there is also potential to apply it to immature coal deposits like lignites, which could provide valuable snapshots of continental climate back to the early Cenozoic. Here results are presented of analyses of different peats in south eastern Canada, showing that the pH of peat along a nutrient gradient is rather well reflected by the CBT. Annual MAT reconstructions based on the MBT/CBT soil calibration, however, tend to overestimate measured MAT. This is also the case for peat analysed from the surface of Etang de la Gruère peat bog in the Swiss Jura Mountains. Along the 6m depth profile of this bog (~13ka), CBT-reconstructed pH is compared with in-situ measured pore water pH showing that the brGDGT composition does not reflect present-day in-situ conditions. Instead, it reflects a stratigraphic boundary between Carex and Sphagnum dominated peat at 4 m depth that is not present in the pore water profile, testifying to a 'fossil' nature of the brGDGTs down the peat bog. Analyses of three immature coals of the Argonne Premium Coal Series reveal that branched GDGTs are present in the most immature coal, the Beulah Zap lignite (Ro = 0.25%), and only just above detection limit in the Wyodak Anderson coal (Ro = 0.32%), both of about the same age (Late Palaeocene). In the more mature Illinois #6 coal (Ro = 0.46%), brGDGTs are completely absent. In the Denver Basin, a comparison is made between outcrop and drilled core samples of Palaeocene lignites. BrGDGTs are preserved in the core samples, although in low quantities compared to peat. Outcrop samples are clearly overprinted by modern soil derived brGDGTs, despite digging a meters deep trench, which shows the need to obtain fresh non-weathered samples by coring. Reconstructed annual MAT for both the Beulah Zap and the Denver Basin lignites are several degrees higher than estimates based on leaf margin and oxygen isotope analyses from the same sites. Both reconstructions do testify, nevertheless, to the warm continental conditions during the early Cenozoic of the central U.S.A.. Although further validation is required, potentially in the form of a specific peat calibration, these results do show potential for application of the MBT/CBT temperature proxy in peat and lignite deposits.

POWDERED ACTIVATED CARBON FROM NORTH DAKOTA LIGNITE: AN OPTION FOR DISINFECTION BY-PRODUCT CONTROL IN WATER TREATMENT PLANTS

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

Daniel J. Stepan; Thomas A. Moe; Melanie D. Hetland

New federal drinking water regulations have been promulgated to restrict the levels of disinfection by-products (DBPs) in finished public water supplies. DBPs are suspected carcinogens and are formed when organic material is partially oxidized by disinfectants commonly used in the water treatment industry. Additional federal mandates are expected in the near future that will further affect public water suppliers with respect to DBPs. Powdered activated carbon (PAC) has traditionally been used by the water treatment industry for the removal of compounds contributing to taste and odor problems. PAC also has the potential to remove naturally occurring organic matter (NOM) frommore » raw waters prior to disinfection, thus controlling the formation of regulated DBPs. Many small water systems are currently using PAC for taste and odor control and have the potential to use PAC for controlling DBPs. This project, a cooperative effort between the Energy & Environmental Research Center (EERC), the Grand Forks Water Treatment Plant, and the University of North Dakota Department of Civil Engineering, consists of several interrelated tasks. The objective of the research was to evaluate a cost-effective PAC produced from North Dakota lignite for removing NOM from water and reducing trihalomethane formation potential. The research approach was to develop a statistically valid testing protocol that can be used to compare dose-response relationships between North Dakota lignite-derived PAC and commercially available PAC products. A statistical analysis was performed to determine whether significant correlations exist between operating conditions, water properties, PAC properties, and dose-response behavior. Pertinent physical and chemical properties were also measured for each of the waters and each of the PACs.« less

Effects of low-temperature catalytic pretreatments on coal structure and reactivity in liquefaction. Final technical report, Volume 1 - effects of solvents, catalysts and temperature conditions on conversion and structural changes of low-rank coals

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

Huang, Lili; Schobert, Harold H.; Song, Chunshan

1998-01-01

The main objectives of this project were to study the effects of low-temperature pretreatments on coal structure and their impacts on subsequent liquefaction. The effects of pretreatment temperatures, catalyst type, coal rank, and influence of solvent were examined. Specific objectives were to identify the basic changes in coal structure induced by catalytic and thermal pretreatments, and to determine the reactivity of the catalytically and thermally treated coals for liquefaction. In the original project management plan it was indicated that six coals would be used for the study. These were to include two each of bituminous, subbituminous, and lignite rank. Formore » convenience in executing the experimental work, two parallel efforts were conducted. The first involved the two lignites and one subbituminous coal; and the second, the two bituminous coals and the remaining subbituminous coal. This Volume presents the results of the first portion of the work, studies on two lignites and one subbituminous coal. The remaining work accomplished under this project will be described and discussed in Volume 2 of this report. The objective of this portion of the project was to determine and compare the effects of solvents, catalysts and reaction conditions on coal liquefaction. Specifically, the improvements of reaction conversion, product distribution, as well as the structural changes in the coals and coal-derived products were examined. This study targeted at promoting hydrogenation of the coal-derived radicals, generated during thermal cleavage of chemical bonds, by using a good hydrogen donor-solvent and an effective catalyst. Attempts were also made in efforts to match the formation and hydrogenation of the free radicals and thus to prevent retrogressive reaction.« less

EERC pilot-scale CFBC evaluation facility Project CFB test results. Topical report, Task 7.30

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

Mann, M.D.; Hajicek, D.R.; Henderson, A.K.

Project CFB was initiated at the University of North Dakota Energy and Environmental Research Center (EERC) in May 1988. Specific goals of the project were to (1) construct a circulating fluidized-bed combustor (CFBC) facility representative of the major boiler vendors` designs with the capability of producing scalable data, (2) develop a database for use in making future evaluations of CFBC technology, and (3) provide a facility for evaluating fuels, free of vendor bias for use in the - energy industry. Five coals were test-burned in the 1-MWth unit: North Dakota and Asian lignites, a Wyoming subbituminous, and Colorado and Pennsylvaniamore » bituminous coats. A total of 54 steady-state test periods were conducted, with the key test parameters being the average combustor temperature, excess air, superficial gas velocity, calcium-to-sulfur molar ratio, and the primary air-to-secondary air split. The capture for a coal fired in a CFBC is primarily dependent upon the total alkali-to-sulfur ratio. The required alkali-to ratio for 90% sulfur retention ranged from 1.4 to 4.9, depending upon coal type. While an alkali-to-ratio of 4.9 was required to meet 90% sulfur retention for the Salt Creek coal versus 1.4 for the Asian lignite, the total amount of sorbent addition required is much less for the Salt Creek coal, 4.2 pound sorbent per million Btu coal input, versus 62 pound/million Btu for the Asian lignite. The bituminous coals tested show optimal capture at combustor temperatures of approximately 1550{degree}F, with low-rank coals having optimal sulfur capture approximately 100{degree}F lower.« less

EERC pilot-scale CFBC evaluation facility Project CFB test results

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

Mann, M.D.; Hajicek, D.R.; Henderson, A.K.

Project CFB was initiated at the University of North Dakota Energy and Environmental Research Center (EERC) in May 1988. Specific goals of the project were to (1) construct a circulating fluidized-bed combustor (CFBC) facility representative of the major boiler vendors' designs with the capability of producing scalable data, (2) develop a database for use in making future evaluations of CFBC technology, and (3) provide a facility for evaluating fuels, free of vendor bias for use in the - energy industry. Five coals were test-burned in the 1-MWth unit: North Dakota and Asian lignites, a Wyoming subbituminous, and Colorado and Pennsylvaniamore » bituminous coats. A total of 54 steady-state test periods were conducted, with the key test parameters being the average combustor temperature, excess air, superficial gas velocity, calcium-to-sulfur molar ratio, and the primary air-to-secondary air split. The capture for a coal fired in a CFBC is primarily dependent upon the total alkali-to-sulfur ratio. The required alkali-to ratio for 90% sulfur retention ranged from 1.4 to 4.9, depending upon coal type. While an alkali-to-ratio of 4.9 was required to meet 90% sulfur retention for the Salt Creek coal versus 1.4 for the Asian lignite, the total amount of sorbent addition required is much less for the Salt Creek coal, 4.2 pound sorbent per million Btu coal input, versus 62 pound/million Btu for the Asian lignite. The bituminous coals tested show optimal capture at combustor temperatures of approximately 1550[degree]F, with low-rank coals having optimal sulfur capture approximately 100[degree]F lower.« less

Nuclear magnetic resonance studies of ancient buried wood-II. Observations on the origin of coal from lignite to bituminous coal

USGS Publications Warehouse

Hatcher, P.G.; Breger, I.A.; Szeverenyi, N.; Maciel, G.E.

1982-01-01

Coalified logs ranging in age from Late Pennsylvania to Miocene and in rank from lignite B to bituminous coal were analyzed by 13C nuclear magnetic resonance (NMR) utilizing the cross-polarization, magic-angle spinning technique, as well as by infrared spectroscopy. The results of this study indicate that at least three major stages of coalification can be observed as wood gradually undergoes transformation to bituminous coal. The first stage involves hydrolysis and loss of cellulose from wood with retention and differential concentration of the resistant lignin. The second stage involves conversion of the lignin residues directly to coalified wood of lignitic rank, during which the oxygen content of intermediate diagenetic products remains constant as the hydrogen content and the carbon content increases. These changes are thought to involve loss of methoxyl groups, water, and C3 side chains from the lignin. In the third major stage of coalification, the coalified wood increases in rank to subbituminous and bituminous coal; during this stage the oxygen content decreases, hydrogen remains constant, and the carbon content increases. These changes are thought to result from loss of soluble humic acids that are rich in oxygen and that are mobilized during compaction and dewatering. Relatively resistant resinous substances are differentially concentrated in the coal during this stage. The hypothesis that humic acids are formed as mobile by-products of the coalification of lignin and function only as vehicles for removal of oxygen represents a dramatic departure from commonly accepted views that they are relatively low-molecular-weight intermediates formed during the degradation of lignin that then condense to form high-molecular-weight coal structures. ?? 1982.

Source apportionment by PMF on elemental concentrations obtained by PIXE analysis of PM10 samples collected at the vicinity of lignite power plants and mines in Megalopolis, Greece

NASA Astrophysics Data System (ADS)

Manousakas, M.; Diapouli, E.; Papaefthymiou, H.; Migliori, A.; Karydas, A. G.; Padilla-Alvarez, R.; Bogovac, M.; Kaiser, R. B.; Jaksic, M.; Bogdanovic-Radovic, I.; Eleftheriadis, K.

2015-04-01

Particulate matter (PM) is an important constituent of atmospheric pollution especially in areas under the influence of industrial emissions. Megalopolis is a small city of 10,000 inhabitants located in central Peloponnese in close proximity to three coal opencast mines and two lignite fired power plants. 50 PM10 samples were collected in Megalopolis during the years 2009-11 for elemental and multivariate analysis. For the elemental analysis PIXE was used as one of the most effective techniques in APM analytical characterization. Altogether, the concentrations of 22 elements (Z = 11-33), whereas Black Carbon was also determined for each sample using a reflectometer. Factorization software was used (EPA PMF 3.0) for source apportionment analysis. The analysis revealed that major emission sources were soil dust 33% (7.94 ± 0.27 μg/m3), biomass burning 19% (4.43 ± 0.27 μg/m3), road dust 15% (3.63 ± 0.37 μg/m3), power plant emissions 13% (3.01 ± 0.44 μg/m3), traffic 12% (2.82 ± 0.37 μg/m3), and sea spray 8% (1.99 ± 0.41 μg/m3). Wind trajectories have suggested that metals associated with emission from the power plants came mainly from west and were connected with the locations of the lignite mines located in this area. Soil resuspension, road dust and power plant emissions increased during the warm season of the year, while traffic/secondary, sea spray and biomass burning become dominant during the cold season.

OXIDATION AND DEVOLATILIZATION OF NITROGEN IN COAL CHAR

EPA Science Inventory

The reactions of organically-bound nitrogen in coal char during combustion have been studied in a laboratory furnace using size-graded char particles prepared by the pyrolysis of a Montana lignite. The time-resolved variations of nitrogen-to-carbon ratio during char oxidation hav...