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Remediation of Uranium-Contaminated Ground Water at Fry Canyon, Utah
Science Highlight – November 2003 Remediation of Uranium-contaminated Ground Water at Fry Canyon, Utah Christopher C. Fuller1, John R. Bargar2, James A. Davis1 1U.S. Geological Survey, Water Resources Division, Menlo Park, CA 2Stanford Synchrotron Radiation Laboratory, SLAC, Stanford University, Stanford, CA Clean up of contaminated aquifers is a difficult and expensive problem because of the inaccessibility of the subsurface and the volume of soil and ground water requiring treat- ment. Established technologies such as pump-and-treat and soil excavation are ineffective in most large contamination scenarios because they treat only a small fraction of the con- tamination or are prohibitively expensive (National Research Council, 1999). Perme- able Reactive Barriers (PRBs) are a relatively new technology that offer promise to overcome these obstacles. PRBs are trenches (figure 1) or fence-like arrays of non-pumping wells emplaced in the subsurface at depths of up to 150 feet to intercept the flow of contaminated ground water (Freethey et al., 2002). Fill materials contained within the PRBs react with dissolved contaminants to degrade or sequester them. Thus, in essence, PRBs act as large in-situ filters to clean ground water. PRB technologies offer lower oper- ating costs, are highly energy efficient, and require no surface facilities or ground water pumping/recharge (Freethey et al., 2002; Morrison and Spangler, 1992; Shoemaker et al., 1995). Two commonly proposed PRB contaminant-removal mechanisms are: (a) precipitation reac- tions in which metal contaminants are sequestered within freshly formed mineral phases, and (b) oxidative degradation of contaminants by particulate iron metal. In order for PRBs to be cost-effective they should be effective for an economically viable period (or be replenishable). -
Iidentilica2tion and Occurrence of Uranium and Vanadium Identification and Occurrence of Uranium and Vanadium Minerals from the Colorado Plateaus
IIdentilica2tion and occurrence of uranium and Vanadium Identification and Occurrence of Uranium and Vanadium Minerals From the Colorado Plateaus c By A. D. WEEKS and M. E. THOMPSON A CONTRIBUTION TO THE GEOLOGY OF URANIUM GEOLOGICAL S U R V E Y BULL E TIN 1009-B For jeld geologists and others having few laboratory facilities.- This report concerns work done on behalf of the U. S. Atomic Energy Commission and is published with the permission of the Commission. UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1954 UNITED STATES DEPARTMENT OF THE- INTERIOR FRED A. SEATON, Secretary GEOLOGICAL SURVEY Thomas B. Nolan. Director Reprint, 1957 For sale by the Superintendent of Documents, U. S. Government Printing Ofice Washington 25, D. C. - Price 25 cents (paper cover) CONTENTS Page 13 13 13 14 14 14 15 15 15 15 16 16 17 17 17 18 18 19 20 21 21 22 23 24 25 25 26 27 28 29 29 30 30 31 32 33 33 34 35 36 37 38 39 , 40 41 42 42 1v CONTENTS Page 46 47 48 49 50 50 51 52 53 54 54 55 56 56 57 58 58 59 62 TABLES TABLE1. Optical properties of uranium minerals ______________________ 44 2. List of mine and mining district names showing county and State________________________________________---------- 60 IDENTIFICATION AND OCCURRENCE OF URANIUM AND VANADIUM MINERALS FROM THE COLORADO PLATEAUS By A. D. WEEKSand M. E. THOMPSON ABSTRACT This report, designed to make available to field geologists and others informa- tion obtained in recent investigations by the Geological Survey on identification and occurrence of uranium minerals of the Colorado Plateaus, contains descrip- tions of the physical properties, X-ray data, and in some instances results of chem- ical and spectrographic analysis of 48 uranium arid vanadium minerals. -
Stillwellite-(Ce) (Ce, La, Ca)Bsio
Stillwellite-(Ce) (Ce; La; Ca)BSiO5 c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Hexagonal. Point Group: 3: As °at rhombohedral crystals, to 4 cm, and massive. Twinning: Observed about [100]. Physical Properties: Cleavage: One imperfect. Fracture: Conchoidal. Hardness = 6.5 D(meas.) = 4.57{4.60 D(calc.) = 4.67 » Optical Properties: Transparent to translucent. Color: Red-brown to pale pink; colorless in thin section. Streak: White. Optical Class: Uniaxial (+) to biaxial (+). ! = 1.765{1.784 ² = 1.780{1.787 2V(meas.) = 0±{6± Cell Data: Space Group: P 31: a = 6.841{6.844 c = 6.700{6.702 Z = 3 X-ray Powder Pattern: Mary Kathleen mine, Australia. 3.43 (s), 2.96 (s), 2.13 (ms), 4.44 (m), 1.864 (m), 2.71 (mw), 2.24 (mw) Chemistry: (1) (2) (1) (2) (1) (2) SiO2 22.40 22.06 La2O3 27.95 19.12 MgO 0.06 UO2 0.22 Ce2O3 33.15 30.82 CaO 0.95 0.34 ThO2 5.41 Pr2O3 1.82 F 0.30 + B2O3 12.23 [13.46] Nd2O3 5.36 H2O 0.85 Al2O3 0.42 Sm2O3 0.34 H2O¡ 0.10 Y2O3 0.74 0.28 Fe2O3 0.18 P2O5 0.67 Total [100.00] [99.26] (1) Mary Kathleen mine, Australia; recalculated to 100.00% after removal of very small amounts of uraninite and apatite determined by separate analysis. (2) Vico volcano, near Vetralla, Italy; by electron microprobe, B2O3 calculated from stoichiometry, original total given as 99.23%; corresponds to (Ce0:50La0:31Nd0:08Th0:05Pr0:03Ca0:02Sm0:01)§=1:00B1:02Si0:97O5: Occurrence: Locally abundant as a metasomatic replacement of metamorphosed calcareous sediments (Mary Kathleen mine, Australia); in alkalic pegmatites in syenite in an alkalic massif (Dara-i-Pioz massif, Tajikistan). -
AUTUNITE from MT. SPOKANE, WASHINGTON* G. W. Lno, U. S. Geologicalsurvey, Menlo Park, California
THE AMERICAN MINERALOGIST, VOL. 45, JANUARY_FEBRUARY, 1960 AUTUNITE FROM MT. SPOKANE, WASHINGTON* G. W. Lno, U. S. GeologicalSurvey, Menlo Park, California ABSTRACT Near Mt. Spokane, Washington, coarsely crystalline autunite is developed in vugs, fractures, and shear zones in granitic rock. With the exception of dispersed submicroscopic uraninite particles, autunite is the only ore mineral in the deposits. A study of associated granitic rocks reveals that apatite, the most abundant accessory constituent, has been pref- erentially leached and corroded in mineralized zones, suggesting that it may have provided a source of lime and phosphate for the formation of autunite. Leaching may have been effected partly by meteoric water) but more probably was due to the action of ascending connate solutions that may also have carried uranium from unoxidized, as yet undiscovered deposits at depth. Autunite from the Daybreak mine has been studied optically, chemically, and by r-ray diffraction. The autunite is commonly zoned from light-yellow margins to dark-green or black cores, and autunite from the inner zone has a higher specific gravity and higher re- fractive indices than peripheral light material. X-ray powder difiraction patterns of dark and light meta-autunite formed from this autunite show no significant difierences in the d spacings; howevet, diffraction patterns of nine zoned samples each show uraninite to be present in the dark, and absent from the light, phase. UOz and UOs determinations range from 0.66-0.70 per cent and 57.9-58.0 pe( cent, respectively, for light autunite, whereas dark autunite shows a range (in seven determinations) of UOz from 1,2 to 4.0 per cent, and UOs from 55.1 to 58.8 per cent. -
Cation Substitution in Uranyl Phosphates of the Autunite Group: Equilibrium Relations and Crystallization Between Metatorbernite and Metauranocircite
Versão online: http://www.lneg.pt/iedt/unidades/16/paginas/26/30/208 Comunicações Geológicas (2015) 102, Especial I, 27-30 ISSN: 0873-948X; e-ISSN: 1647-581X Cation substitution in uranyl phosphates of the autunite group: equilibrium relations and crystallization between metatorbernite and metauranocircite Substituição catiónica em fosfatos de uranilo do grupo da autunite: relações de equilíbrio e cristalização entre metatorbernite e metauranocircite M. Andrade1, J. Duarte1, I. Martins 1, J. Reis 1, J. Mirão3, M. A. Gonçalves1,2* Artigo original Original article © 2015 LNEG – Laboratório Nacional de Geologia e Energia IP Abstract: Uranyl phosphate minerals play an important role in the 1. Introduction uranium immobilization within weathering and supergene enrichment profiles. This work consists on the morphological, structural and Uranyl phosphate minerals are major constituents in weathered U chemical characterization of natural and synthetic minerals of Cu and Ba deposits and can display a multi-stage evolving history in the – metatorbernite and metauranocircite, respectively. SEM imaging has environment they crystalize. Their importance is two-fold: as revealed an extended range of morphologies, from tabular to rosette-like main U-bearing phases in weathering profiles with potential crystals, with the presence of epitaxial growths. These studies have also economic value (as in Nisa and Tarabau, where natural uranyl revealed natural heterogeneities affected by cationic substitution along phosphates of Cu and Ba were identified; Pinto et al., 2012; preferred crystallographic directions. The experimental results suggest Prazeres, 2011) and as fixing phases of U limiting its long-term, that the precipitation of metatorbernite is easier than metauranocircite. Simulations of the chemical system show that precipitation depends on million-year scale, dispersion in the oxidized surface supersaturation evolution, which in turn in a function of aqueous complex environment. -
Three Occurrences of High-Thorian Uraninite Near Easton, Pennsylvania*
THE AMERICAN MINERALOGIST, YOL. 42, NOVEMBER_DECEMBER 1957 THREE OCCURRENCES OF HIGH-THORIAN URANINITE NEAR EASTON, PENNSYLVANIA* Anruun M oNrcounnu, Laf ayette C oll,ege, Easton, P ennsylaanio. Assrnacr The geology, mineralogy and paragenesis of three occurrences of high-thorian uraninite in serpentine near Easton, Pa., are described. seven *-ray fluorescence analyses together with three corroborative chemical analyses show this mineral to be high-thorian uraninite rather than high-uranoan thorianite as supposed six samples contajn from about l5/o to 3570ThOr. At the Williams quarry hydrothermai alteration of much uraninite to a sequence of secondary uranium- and thorium-rich minerals occurred. Frondel,s Mineral C, thoro- gummite, then boltrvoodite and uranophane were formed during serpentinization of frac- tured dolomite-diopside-tremolite contact-metamorphosed rock. Supergene coatings, chiefly hydrous uranium silicates and including boltwoodite and uranophane, formed much later. At the reservoir site slight hldrothermal alteration oI uraninite to thorogummite occurred. At the Royal Green Marble co. quarry uraninite is found unaltered. At these localities fracturing or temperatures during later hydrothermal mineralization may have been of lower intensity. It is concluded that thorium-rich Easton uraninite does not alter readily to secondary minerals, except when subjected to severe deformation and concomitant attack by ser- pentinizing hydrothermal solutions. The Th, rJ and. zr of this contact-metasomatic uran- inite and the associated zircon originated in a granite-pegmatite magma rich in these elements, which intruded dolomitic rocks and through deformation while crystallizing yielded the hydrothermal solutions that deposited these minerals in those rocks. then serpentinized the rocks. INrnonucrroN High-thorian uraninite, regardeduntil now as high-uranoan thorian- ite,1occurs in serpentinerock at three localitiesjust north and northeast of Easton, Pennsylvania.The two earlier discoverieswere made around 1930by GeorgeW. -
Petrology and Mineralogy of the Mount Rosa Area, El Paso and Teller Counties, Colorado
THE AMERICAN MINERALOGIST, VOL. 5 1, MARCH-APRIL, 1966 PETROLOGY AND MINERALOGY OF THE MOUNT ROSA AREA, EL PASO AND TELLER COUNTIES, COLORADO. II. PEGMATITESI EuceNB B. Gnoss, CaliJornia Diris,ion of Mines and Geology San Fra nci sco, C alifor n i o AND E. Wu. IIerNnrcu, Department of Geologyand Mineralogy The Llniversity of Michigan, Ann Arbor, Michigan. Aesrnlcr Two contrasting swarms of pegmatite dikes occur intermingled in the Pikes Peak granite and in related alkalic granites in the Mount Rosa area, west of Colorado Springs. One is the older calc-alkalic Pikes Peak type; the younger is the alkalic Mount Rosa type. The accessory assemblage of the Mount Rosa quartz-microcline-riebeckite pegmatites consists chiefly of radioactive zircon, fluorite, astrophyllite, thorite, and lesser amounts of pyrochlore, rutile, niobian rutile, columbite, bertrandite and rare aluminofluorides. These dikes intrude both the Pikes Peak and its derivative fayaiite granites along north- east-trending fractures. These pegmatites contrast markedly with the coexisting Pikes Peak pegmatites, which are characterized by quartz and amazonite crystals, zircon, biotite, siderite, and minor topaz, allanite, cassiterite and genthelvite. The Pikes Peak type occurs as segregations and injected bodies only within Pikes Peak granite. Age determinations on zircons from pegmatites of the Mount Rosa type proved to be inconsistent, but ages determined by means of the Kao/Ara0 method on pegmatitic rie- beckite are consistent rvith geological evidence and age determinations on the granites, giving an age of 1040 my. INrnolucrroN Discoverl' of unusual minerals in pegmatitesof the St. Peters Dome district, Mount Rosa area,Colorado, attracted the attention of mineralo- gists as earlv as 1877 (Koenig, 1877). -
Spodumene and Autunite from Alstead, New Hampshire G
578 TEE AM ERICAN M I N ERALOGIST SPODUMENE AND AUTUNITE FROM ALSTEAD, NEW HAMPSHIRE G. R. MBcarHLrN, Cornel'|,Uniaersity. During an investigation in August and September, 7927, oI the pegmatites of the Gilsum area, Cheshire County, New Hamp- shire, two minerals, spodumene and autunite, were found which are not known to have been reported before from this district. It seemsworthwhile, therefore, to put this occurrence on record. The pegmatites of this region are intruded into a mica schist with which they have rather sharp contacts, although there is some lit-par-lit injection on a small scale as well as tourmalini- zation of the wall rock. The essentialminerals, aside from qtartz, are feldspar and muscovite, both of which are extensively quarried in the area. The accessory minerals include biotite, black tour- maline, beryl, garnet, apatite, spodumene,autunite, and zircon. The spodumene and autunite came from the quarry of the New Hampshire Mica and Mining Company in the town of Alstead, about one and four-fifths miles north northwest of Gilsum village. The spodumene crystals occur on an inaccessiblewall near the top of the west face of the quarry. They were much concealedby material washed down from the surface, but the crystals exposed appeared to be of the order of several feet in length. From blocks which had fallen from the wall a few crystals were obtained, the largest of which was six inches long, four inches wide, and one and one-half inches thick, but it did not represent the entire crystal. The spodumene occurs associated with tourmaline, garnet, apatite, feldspar, qtartz, and sericite. -
Thermodynamics of Formation of Coffinite, Usio4
Thermodynamics of formation of coffinite, USiO4 Xiaofeng Guoa,b, Stéphanie Szenknectc, Adel Mesbahc, Sabrina Labsd, Nicolas Clavierc, Christophe Poinssote, Sergey V. Ushakova, Hildegard Curtiusd, Dirk Bosbachd, Rodney C. Ewingf, Peter C. Burnsg, Nicolas Dacheuxc, and Alexandra Navrotskya,1 aPeter A. Rock Thermochemistry Laboratory and Nanomaterials in the Environment, Agriculture, and Technology Organized Research Unit, University of California, Davis, CA 95616; bEarth and Environmental Sciences Division, Los Alamos National Laboratory, Los Alamos, NM 87545; cInstitut de Chimie Séparative de Marcoule, UMR 5257, CNRS/CEA/Université Montpellier/Ecole Nationale Supérieure de Chimie de Montpellier, Site de Marcoule, 30207 Bagnols sur Cèze, France; dInstitute of Energy and Climate Research, Nuclear Waste Management, Forschungszentrum Jülich GmbH, 52425 Jülich, Germany; eCEA, Nuclear Energy Division, RadioChemistry & Processes Department, BP 17171, 30207 Bagnols sur Cèze, France; fDepartment of Geological and Environmental Sciences, School of Earth Sciences, Stanford University, Stanford, CA 94305; and gDepartment of Civil and Environmental Engineering and Earth Sciences, University of Notre Dame, Notre Dame, IN 46556 Contributed by Alexandra Navrotsky, April 20, 2015 (sent for review February 10, 2015) Coffinite, USiO4, is an important U(IV) mineral, but its thermody- The precipitation of USiO4 as a secondary phase should be namic properties are not well-constrained. In this work, two dif- favored in contact with silica-rich groundwater (21) [silica − ferent coffinite samples were synthesized under hydrothermal concentration >10 4 mol/L (22, 23)]. Natural coffinite samples conditions and purified from a mixture of products. The enthalpy are often fine-grained (4, 5, 8, 11, 13, 15, 24), due to the long of formation was obtained by high-temperature oxide melt solu- exposure to alpha-decay event irradiation (4, 6, 25, 26) and are tion calorimetry. -
Meta-Autunite Ca(UO2)2(PO4)2 • 2−6H2O C 2001-2005 Mineral Data Publishing, Version 1
Meta-autunite Ca(UO2)2(PO4)2 • 2−6H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Tetragonal. Point Group: 4/m 2/m 2/m or 422. As rectangular tabular crystals, exhibiting {001}, {111}, {110}, {011}, rarely pyramidal; as foliated or scaly aggregates. Physical Properties: Cleavage: Perfect on {001}; indistinct on {010}. Hardness = 2–2.5 D(meas.) = 3.35–3.55 D(calc.) = 3.31 Radioactive. Fluoresces yellowish green under UV. Dehydrates irreversibly from autunite under ambient conditions. Optical Properties: Translucent to opaque. Color: Lemon-yellow to greenish yellow, yellowish green, dark green. Luster: Pearly to dull. Optical Class: Uniaxial (–), anomalously biaxial (–). Pleochroism: X = colorless to pale yellow; Y = Z = dark yellow. Orientation: Z = c. Dispersion: r> v,strong. ω = 1.600–1.611 = 1.594–1.598 α = 1.596–1.604 β = 1.602–1.622 γ = 1.603–1.630 2V(meas.) = 5–20◦ Cell Data: Space Group: P 4/nmm or P 4222. a = 6.99 c = 8.46 Z = 1 X-ray Powder Pattern: Les Oudots mine, Saˆone-et-Loire,France. (ICDD 39-1351). 8.46 (100), 3.620 (60), 2.115 (35), 2.615 (30), 1.601 (25), 5.39 (20), 4.233 (20) Chemistry: (1) The mineral usually analyzed as autunite; meta-autunite I contains 6H2O; meta-autunite II contains 2H2O and probably does not occur in nature. Mineral Group: Meta-autunite group. Occurrence: A secondary mineral, formed as dehydration pseudomorphs after autunite. Association: Autunite. Distribution: Widespread. All autunite (q.v.) localities probably contain meta-autunite. Name: The prefix meta indicates the dehydration product of autunite. -
Trace- and Minor-Element Mineralogy of the Microgranite at Ghurayyah
DEPARTMENT OF THE INTERIOR U.S. GEOLOGICAL SURVEY Trace- and minor-element mineralogy of the microgranite at Ghurayyah, Kingdom of Saudi Arabia I/ I/ Mortimer H. Staatz and Isabelle K. Brownfield Open-File Report 86- Report prepared for Ministry of Petroleum and Mineral Resources, Deputy Ministry for Mineral Resources, Saudi Arabia This report is preliminary and has not been reviewed for conformity with U.S. Geological Survey editorial standards and stratigraphic nomenclature. I/ U.S. Geological Survey, Denver, CO 1986 CONTENTS ABSTRACT........................................................... 1 INTRODUCTION....................................................... 1 MINERAL-SEPARATION STUDIES......................................... 4 AUTORADIOGRAPHS.................................................... 6 INDIVIDUAL-GRAIN STUDIES........................................... 6 GRAIN-SIZE STUDIES................................................. 12 DATA STORAGE....................................................... 12 REFERENCES CITED................................................... 12 ILLUSTRATIONS Figure 1 Index map showing the location of Ghurayyah.............. 2 2 Autoradiographs of samples from Ghurayyah................ 7 TABLES Table 1 Location and type of samples collected at Ghurayyah....... 3 2 Minerals identified in heavy-mineral separates from Ghurayyah................................................. 5 3 Electron-microprobe analyses of zircon from Ghurayyah..... 9 4 Electron-microprobe analyses of thorite grains from sample G-l, -
Coffinite Formation from UO2+X
www.nature.com/scientificreports OPEN Cofnite formation from UO2+x Stéphanie Szenknect1*, Delhia Alby1, Marta López García2, Chenxu Wang4, Renaud Podor1, Frédéric Miserque5, Adel Mesbah1, Lara Duro2, Lena Zetterström Evins3, Nicolas Dacheux1, Jordi Bruno2 & Rodney C. Ewing4 Most of the highly radioactive spent nuclear fuel (SNF) around the world is destined for fnal disposal in deep-mined geological repositories. At the end of the fuel’s useful life in a reactor, about 96% of the SNF is still UO2. Thus, the behaviour of UO2 in SNF must be understood and evaluated under the weathering conditions of geologic disposal, which extend to periods of hundreds of thousands of years. There is ample evidence from nature that many uranium deposits have experienced conditions for which the formation of cofnite, USiO4, has been favoured over uraninite, UO2+x, during subsequent alteration events. Thus, cofnite is an important alteration product of the UO2 in SNF. Here, we present the frst evidence of the formation of cofnite on the surface of UO2 at the time scale of laboratory experiments in a solution saturated with respect to amorphous silica at pH = 9, room temperature and under anoxic conditions. 4+ Uraninite, UO2+x is the most common U mineral in nature followed by cofnite, USiO 4, which is found as a primary phase or an alteration product in many uranium deposits. Cofnite, tetragonal, is isostructural with 1 zircon (ZrSiO4) and thorite (TSiO 4); however, cofnite can contain some water either as H 2O or OH groups . Altered uraninite and cofnite have been documented from Oklo, Gabon 2–5, deposits in the Athabasca Basin 4,6,7 and Elliot Lake, Canada8.