Iidentilica2tion and Occurrence of Uranium and Vanadium Identification and Occurrence of Uranium and Vanadium Minerals from the Colorado Plateaus
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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). -
Significance of Mineralogy in the Development of Flowsheets for Processing Uranium Ores
JfipwK LEACHING TIME REAGENTS TEMPERATURE FLOCCULANT CLARITY AREA COUNTER CURRENT DECANTATION It 21 21 J^^LJt TECHNICAL REPORTS SERIES No.19 6 Significance of Mineralogy in the Development of Flowsheets for Processing Uranium Ores \W# INTERNATIONAL ATOMIC ENERGY AGENCY, VIENNA, 1980 SIGNIFICANCE OF MINERALOGY IN THE DEVELOPMENT OF FLOWSHEETS FOR PROCESSING URANIUM ORES The following States are Members of the International Atomic Energy Agency: AFGHANISTAN HOLY SEE PHILIPPINES ALBANIA HUNGARY POLAND ALGERIA ICELAND PORTUGAL ARGENTINA INDIA QATAR AUSTRALIA INDONESIA ROMANIA AUSTRIA IRAN SAUDI ARABIA BANGLADESH IRAQ SENEGAL BELGIUM IRELAND SIERRA LEONE BOLIVIA ISRAEL SINGAPORE BRAZIL ITALY SOUTH AFRICA BULGARIA IVORY COAST SPAIN BURMA JAMAICA SRI LANKA BYELORUSSIAN SOVIET JAPAN SUDAN SOCIALIST REPUBLIC JORDAN SWEDEN CANADA KENYA SWITZERLAND CHILE KOREA, REPUBLIC OF SYRIAN ARAB REPUBLIC COLOMBIA KUWAIT THAILAND COSTA RICA LEBANON TUNISIA CUBA LIBERIA TURKEY CYPRUS LIBYAN ARAB JAMAHIRIYA UGANDA CZECHOSLOVAKIA LIECHTENSTEIN UKRAINIAN SOVIET SOCIALIST DEMOCRATIC KAMPUCHEA LUXEMBOURG REPUBLIC DEMOCRATIC PEOPLE'S MADAGASCAR UNION OF SOVIET SOCIALIST REPUBLIC OF KOREA MALAYSIA REPUBLICS DENMARK MALI UNITED ARAB EMIRATES DOMINICAN REPUBLIC MAURITIUS UNITED KINGDOM OF GREAT ECUADOR MEXICO BRITAIN AND NORTHERN EGYPT MONACO IRELAND EL SALVADOR MONGOLIA UNITED REPUBLIC OF ETHIOPIA MOROCCO CAMEROON FINLAND NETHERLANDS UNITED REPUBLIC OF FRANCE NEW ZEALAND TANZANIA GABON NICARAGUA UNITED STATES OF AMERICA GERMAN DEMOCRATIC REPUBLIC NIGER URUGUAY GERMANY, FEDERAL REPUBLIC OF NIGERIA VENEZUELA GHANA NORWAY VIET NAM GREECE PAKISTAN YUGOSLAVIA GUATEMALA PANAMA ZAIRE HAITI PARAGUAY ZAMBIA PERU The Agency's Statute was approved on 23 October 1956 by the Conference on the Statute of the IAEA held at United Nations Headquarters, New York; it entered into force on 29 July 1957. -
Diaspore Alo(OH) C 2001-2005 Mineral Data Publishing, Version 1 Crystal Data: Orthorhombic
Diaspore AlO(OH) c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Orthorhombic. Point Group: 2/m 2/m 2/m. As crystals, platy on {010} and elongated to acicular along [001], to 40 cm; stalactitic, foliated, scaly; disseminated, massive. Twinning: On {021}, to form heart-shaped twins or pseudohexagonal aggregates; on {061}, uncommon. Physical Properties: Cleavage: {010} perfect, {110} distinct, {100} in traces. Fracture: Conchoidal. Tenacity: Very brittle. Hardness = 6.5–7 D(meas.) = 3.2–3.5 D(calc.) = 3.380 Optical Properties: Transparent to translucent. Color: White, pale gray, colorless, greenish gray, brown, pale yellow, pink, lilac; color may vary with viewing direction in the same specimen, may show a color change from brownish green in daylight to raspberry pink in artificial light; colorless in thin section. Luster: Adamantine, vitreous, pearly on cleavage faces. Optical Class: Biaxial (+). Pleochroism: In thick plates, may be reddish brown to reddish violet; grayish green to green. Orientation: X = c; Y = b; Z = a. Dispersion: r< v,weak. Absorption: Z > Y > X, seen on strongly colored specimens. α = 1.682–1.706 β = 1.705–1.725 γ = 1.730–1.752 2V(meas.) = 84◦–86◦ Cell Data: Space Group: P bnm. a = 4.4007(6) b = 9.4253(13) c = 2.8452(3) Z = 4 X-ray Powder Pattern: Springfield, Massachusetts, USA. 3.99 (100), 2.317 (56), 2.131 (52), 2.077 (49), 1.633 (43), 2.558 (30), 1.480 (20) Chemistry: (1) (2) (1) (2) SiO2 0.42 Fe2O3 0.18 Al2O3 84.44 84.98 H2O 14.99 15.02 Total 100.03 100.00 (1) Kossoi Brod, Russia. -
A Study of Some Methods of Concentrating Uranium and Radium in Carnotite Ore
Scholars' Mine Masters Theses Student Theses and Dissertations 1932 A study of some methods of concentrating uranium and radium in carnotite ore H. L. Gibbs Follow this and additional works at: https://scholarsmine.mst.edu/masters_theses Part of the Chemical Engineering Commons Department: Recommended Citation Gibbs, H. L., "A study of some methods of concentrating uranium and radium in carnotite ore" (1932). Masters Theses. 4815. https://scholarsmine.mst.edu/masters_theses/4815 This thesis is brought to you by Scholars' Mine, a service of the Missouri S&T Library and Learning Resources. This work is protected by U. S. Copyright Law. Unauthorized use including reproduction for redistribution requires the permission of the copyright holder. For more information, please contact [email protected]. A STUDY OF SOl.ill T,::ETHODS O:B" COl1C}~;TTRl~TnTG TJP"':~..1TTIJL! ;:J·TD RIillIOIJ IN C.AR~OTIT!~ ORE. by lliJ10LD L. GIBBS A THESIS submitted to the faculty of the SCI-TOOL OF MINES AND 1~'IETIJ:.,LURGY OF THE m·...lVERSITY OJ!' I'~IaSOURI in partial fulfillment of the work required for the Degree of' Ivll~T:ER OF SCIENCE n~ C:EIa1IC.AL ENGnmERnTG Rolla, ~~iissour1 1 9 3 2 Al'proved by f.A.J. -,. ~ Acknowledgments • • • • • • • 1 Object • • ••• • • • 2 Introduction • • • 2 Description of the Ore • • • 3 Examination o~ the Ore • • • • • 3 Methods of Analysis • • • • • • 7 Flocculation Tests • • • g Flotation of Carnotite • • • • • II Results of Flotation Testa • • • • 15 Recovery of Radium :rrom Leached Ore by Flotation • • • • 18 Summary -
Roscoelite K(V ; Al; Mg)2Alsi3o10(OH)2 C 2001 Mineral Data Publishing, Version 1.2 ° Crystal Data: Monoclinic
3+ Roscoelite K(V ; Al; Mg)2AlSi3O10(OH)2 c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Monoclinic. Point Group: 2=m: As minute scales, in druses, rosettes, or fan-shaped groups; ¯brous and in felted aggregates; as impregnations, massive. Physical Properties: Cleavage: Perfect on 001 . Hardness = Soft. D(meas.) = 2.92{2.94 D(calc.) = [2.89] f g Optical Properties: Transparent to translucent. Color: Dark clove-brown, greenish brown to dark greenish brown. Luster: Pearly. Optical Class: Biaxial ({). Pleochroism: X = green-brown; Y = Z = olive-green. ® = 1.59{1.610 ¯ = 1.63{1.685 ° = 1.64{1.704 2V(meas.) = 24.5±{39.5± Cell Data: Space Group: C2=c: a = 5.26 b = 9.09 c = 10.25 ¯ = 101:0± Z = 2 X-ray Powder Pattern: Paradox Valley, Colorado, USA. 10.0 (100), 4.54 (80), 3.35 (80), 2.60 (80), 1.52 (60), 3.66 (50), 3.11 (50) Chemistry: (1) SiO2 47.82 Al2O3 12.60 V2O5 19.94 FeO 3.30 MgO 2.43 CaO trace Na2O 0.33 K2O 8.03 + H2O 5.13 Total 99.58 (1) Stuckslager mine, California, USA. Polymorphism & Series: Forms a series with muscovite; 1M polytype. Mineral Group: Mica group. Occurrence: An early-stage gangue mineral in low-temperature epithermal Au-Ag-Te deposits; from the oxidized portions of low-temperature sedimentary U-V ores. Association: Quartz, pyrite, carbonates, °uorite, gold (Au-Ag-Te mineral association); corvusite, hewettite, carnotite, tyuyamunite (U-V mineral association). Distribution: In the USA, from the Stuckslager mine, Lotus, El Dorado Co., California; in Colorado, from Cripple Creek, Teller Co., La Plata district, La Plata Co., Magnolia district, Boulder Co., the Gateway district, Mesa Co., in the Uravan and Paradox, Bull Canyon, and Slick Rock districts, in Montrose, San Miguel, and Dolores Cos. -
Uraninite Alteration in an Oxidizing Environment and Its Relevance to the Disposal of Spent Nuclear Fuel
TECHNICAL REPORT 91-15 Uraninite alteration in an oxidizing environment and its relevance to the disposal of spent nuclear fuel Robert Finch, Rodney Ewing Department of Geology, University of New Mexico December 1990 SVENSK KÄRNBRÄNSLEHANTERING AB SWEDISH NUCLEAR FUEL AND WASTE MANAGEMENT CO BOX 5864 S-102 48 STOCKHOLM TEL 08-665 28 00 TELEX 13108 SKB S TELEFAX 08-661 57 19 original contains color illustrations URANINITE ALTERATION IN AN OXIDIZING ENVIRONMENT AND ITS RELEVANCE TO THE DISPOSAL OF SPENT NUCLEAR FUEL Robert Finch, Rodney Ewing Department of Geology, University of New Mexico December 1990 This report concerns a study which was conducted for SKB. The conclusions and viewpoints presented in the report are those of the author (s) and do not necessarily coincide with those of the client. Information on SKB technical reports from 1977-1978 (TR 121), 1979 (TR 79-28), 1980 (TR 80-26), 1981 (TR 81-17), 1982 (TR 82-28), 1983 (TR 83-77), 1984 (TR 85-01), 1985 (TR 85-20), 1986 (TR 86-31), 1987 (TR 87-33), 1988 (TR 88-32) and 1989 (TR 89-40) is available through SKB. URANINITE ALTERATION IN AN OXIDIZING ENVIRONMENT AND ITS RELEVANCE TO THE DISPOSAL OF SPENT NUCLEAR FUEL Robert Finch Rodney Ewing Department of Geology University of New Mexico Submitted to Svensk Kämbränslehantering AB (SKB) December 21,1990 ABSTRACT Uraninite is a natural analogue for spent nuclear fuel because of similarities in structure (both are fluorite structure types) and chemistry (both are nominally UOJ. Effective assessment of the long-term behavior of spent fuel in a geologic repository requires a knowledge of the corrosion products produced in that environment. -
Arizona Department of Mines and Mineral Resources
Arizona Department of Mines and Mineral Resources 1502 West Washington, Phoenix, AZ 85007 Phone (602) 255-3795 1-800-446-4259 in Arizona FAX (602) 255-3777 www.admmr.state.az.us Titanium Circular 9, August 1982 by Michael N Greeley, Mining Engineer Titanium is a lightweight metal that is virtually as strong as steel. As our technologies and industries have become increasingly sophisticated, demand for this relatively scarce, but highly desirable metal has increased rapidly. This information circular is written to acquaint the prospector and miner with titanium and its uses. A resume of typical geologic environments and production possibilities in Arizona is given. Uses phisticated needs will vie for a greater share of the The largest market for titanium is in the manufacture world's supply of this unique metal. of pigments. Because of its high refractive index, titanium dioxide pigment imparts whiteness, opacity, Geology and Mineralogy and brightness to paints, varnishes, and lacquers. The most important titanium minerals are anatase Titanium pigment is also used greatly in paper coat (Ti0 ), ilmenite (FeTi0 ), perovskite (CaTi03), ru- 2 3 ings and as paper fillers. Many plastic products such tile (Ti0 ), sphene (CaTiSiOS), and leucoxene. Leu as polyethylene, polyvinyl chloride, and polystyrene 2 coxene, a mineraloid, is an alteration product of il incorporate titanium pigment because of its resis menite, from which a portion of the iron has been tance to degradation by ultraviolet light and its leached. Currently the minerals of commercial inter chemical inertness. est are ilmenite, leucoxene, and rutile. Production historically has come from three types of deposits: Titanium dioxide pigment and other titanium com Beach and stream placers, massive deposits of titani pounds are used in many miscellaneous applications, ferous iron ore, and igneous complexes in which ru including rubber tires, floor and wall coverings, tile occurs in association with anorthosite and simi glass fibers, ceramic capacitors, carbide cutting lar, mafic crystalline rocks. -
The Structure and Vibrational Spectroscopy of Cryolite, Na3alf6 Cite This: RSC Adv., 2020, 10, 25856 Stewart F
RSC Advances PAPER View Article Online View Journal | View Issue The structure and vibrational spectroscopy of cryolite, Na3AlF6 Cite this: RSC Adv., 2020, 10, 25856 Stewart F. Parker, *a Anibal J. Ramirez-Cuesta b and Luke L. Daemenb Cryolite, Na3[AlF6], is essential to commercial aluminium production because alumina is readily soluble in molten cryolite. While the liquid state has been extensively investigated, the spectroscopy of the solid state has been largely ignored. In this paper, we show that the structure at 5 K is the same as that at Received 31st May 2020 room temperature. We use a combination of infrared and Raman spectroscopies together with inelastic Accepted 1st July 2020 neutron scattering (INS) spectroscopy. The use of INS enables access to all of the modes of Na3[AlF6], DOI: 10.1039/d0ra04804f including those that are forbidden to the optical spectroscopies. Our spectral assignments are supported rsc.li/rsc-advances by density functional theory calculations of the complete unit cell. Introduction In view of the technological importance of cryolite, we have Creative Commons Attribution 3.0 Unported Licence. carried out a comprehensive spectroscopic investigation and 1 Cryolite, Na3[AlF6], occurs naturally as a rare mineral. Histori- report new infrared and Raman spectra over extended temper- cally, it was used as a source of aluminium but this has been ature and spectral ranges and the inelastic neutron scattering superseded by bauxite (a mixture of the Al2O3 containing (INS) spectrum. The last of these is observed for the rst time minerals boehmite, diaspore and gibbsite), largely because of and enables access to all of the modes of Na3[AlF6]. -
Geochemistry, Mineralogy and Microbiology of Cobalt in Mining-Affected Environments
minerals Article Geochemistry, Mineralogy and Microbiology of Cobalt in Mining-Affected Environments Gabriel Ziwa 1,2,*, Rich Crane 1,2 and Karen A. Hudson-Edwards 1,2 1 Environment and Sustainability Institute, University of Exeter, Penryn TR10 9FE, UK; [email protected] (R.C.); [email protected] (K.A.H.-E.) 2 Camborne School of Mines, University of Exeter, Penryn TR10 9FE, UK * Correspondence: [email protected] Abstract: Cobalt is recognised by the European Commission as a “Critical Raw Material” due to its irreplaceable functionality in many types of modern technology, combined with its current high-risk status associated with its supply. Despite such importance, there remain major knowledge gaps with regard to the geochemistry, mineralogy, and microbiology of cobalt-bearing environments, particu- larly those associated with ore deposits and subsequent mining operations. In such environments, high concentrations of Co (up to 34,400 mg/L in mine water, 14,165 mg/kg in tailings, 21,134 mg/kg in soils, and 18,434 mg/kg in stream sediments) have been documented. Co is contained in ore and mine waste in a wide variety of primary (e.g., cobaltite, carrolite, and erythrite) and secondary (e.g., erythrite, heterogenite) minerals. When exposed to low pH conditions, a number of such minerals are 2+ known to undergo dissolution, typically forming Co (aq). At circumneutral pH, such aqueous Co can then become immobilised by co-precipitation and/or sorption onto Fe and Mn(oxyhydr)oxides. This paper brings together contemporary knowledge on such Co cycling across different mining environments. -
A New Method of the Qualitative Chemical Analysis of Common Cations
A New Method of the Qualitative Chemical Analysis of Common Cations by Keiichiro MATS UOKA* Introductory A qualitative analysis of inorganic substances is concerned with the methods of determining the species of base-forming and acid-forming constituents that are pre- sent in a substance. A qualitative analysis admits of twofold classification ; one is chemical and the other is physical method. Recent progress has introduced into the physical method many useful instruments and, for this reason, it is possible for the physical method to perform a very minute analysis in the accurate manner. Yet these instruments are regrettably too high to be within the reach of an average chemical laboratory. In any qualitative chemical analysis important procedures are separation, detec- tion and confirmatory test of the obtained result. With this method it is imperative that a very minute and accurate determination should be performed in less time. A chemical method is also divided into two kinds ; dry and wet methods. The former consists of heating test which contains blowpipe test as a sub-class and bead reaction including borax bead test, microscopic bead test, etc. Though the dry method is useful, its main value is derived from being used as a preliminary procedure. The latter method is further divided into four classes as follows. 1. Method by the use of H2S. 2. Method which uses substitutes for H2S. 3. Method which uses organic reagents instead of sulfide. 4. Method which detects each element on an individual basis. Methods in (1), (2) and (3) are systematic separating methods. And method in (1) and (2) are analyses based on the same principle. -
Cobalt Mineral Ecology
American Mineralogist, Volume 102, pages 108–116, 2017 Cobalt mineral ecology ROBERT M. HAZEN1,*, GRETHE HYSTAD2, JOSHUA J. GOLDEN3, DANIEL R. HUMMER1, CHAO LIU1, ROBERT T. DOWNS3, SHAUNNA M. MORRISON3, JOLYON RALPH4, AND EDWARD S. GREW5 1Geophysical Laboratory, Carnegie Institution, 5251 Broad Branch Road NW, Washington, D.C. 20015, U.S.A. 2Department of Mathematics, Computer Science, and Statistics, Purdue University Northwest, Hammond, Indiana 46323, U.S.A. 3Department of Geosciences, University of Arizona, 1040 East 4th Street, Tucson, Arizona 85721-0077, U.S.A. 4Mindat.org, 128 Mullards Close, Mitcham, Surrey CR4 4FD, U.K. 5School of Earth and Climate Sciences, University of Maine, Orono, Maine 04469, U.S.A. ABSTRACT Minerals containing cobalt as an essential element display systematic trends in their diversity and distribution. We employ data for 66 approved Co mineral species (as tabulated by the official mineral list of the International Mineralogical Association, http://rruff.info/ima, as of 1 March 2016), represent- ing 3554 mineral species-locality pairs (www.mindat.org and other sources, as of 1 March 2016). We find that cobalt-containing mineral species, for which 20% are known at only one locality and more than half are known from five or fewer localities, conform to a Large Number of Rare Events (LNRE) distribution. Our model predicts that at least 81 Co minerals exist in Earth’s crust today, indicating that at least 15 species have yet to be discovered—a minimum estimate because it assumes that new minerals will be found only using the same methods as in the past. Numerous additional cobalt miner- als likely await discovery using micro-analytical methods. -
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American Mineralogist, Volume 77, pages 670475, 1992 NEW MINERAL NAMES* JonN L. J,Annson CANMET, 555 Booth Street,Ottawa, Ontario KIA OGl' Canada Abswurmbachite* rutile, hollandite, and manganoan cuprian clinochlore. The new name is for Irmgard Abs-Wurmbach, in recog- T. Reinecke,E. Tillmanns, H.-J. Bernhardt (1991)Abs- her contribution to the crystal chemistry, sta- wurmbachite, Cu'?*Mnl*[O8/SiOo],a new mineral of nition of physical properties ofbraunite. Type the braunite group: Natural occurrence,synthesis, and bility relations, and crystal structure.Neues Jahrb. Mineral. Abh., 163,ll7- material is in the Smithsonian Institution, Washington, r43. DC, and in the Institut fiir Mineralogie, Ruhr-Universitlit Bochum, Germany. J.L.J. The new mineral and cuprian braunit€ occur in brown- ish red piemontite-sursassitequartzites at Mount Ochi, near Karystos, Evvia, Greece, and in similar quartzites on the Vasilikon mountains near Apikia, Andros Island, Barstowite* Greece.An electron microprobe analysis (Andros mate- C.J. Stanley,G.C. Jones,A.D. Hart (1991) Barstowite, gave SiO, 9.8, TiO, rial; one of six for both localities) 3PbClr'PbCOr'HrO, a new mineral from BoundsClifl 0.61,Al,O3 0.60, Fe'O, 3.0,MnrO. 71.3,MgO 0.04,CuO St. Endellion,Cornwall. Mineral. Mag., 55, l2l-125. 12.5, sum 97.85 wto/o,corresponding to (CuStrMn3tu- Electron microprobe and CHN analysis gavePb75.47, Mgoo,)", oo(Mn3jrFe|jrAlo orTif.[nCuStr)", nrSi' o, for eight (calc.)6.03, sum 101.46wto/o, cations,ideally CuMnuSiO'r, the Cu analogueof braunite. Cl 18.67,C l.Iz,H 0.18,O to Pb.orClrrrCr.or- The range of Cu2* substitution for Mn2' is 0-42 molo/oin which for 17 atoms corresponds The min- cuprian braunite and 52-93 molo/oin abswurmbachite.