Tables of Fluorescent and Radioactive Minerals
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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. -
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 -
Geochemical Modeling of Iron and Aluminum Precipitation During Mixing and Neutralization of Acid Mine Drainage
minerals Article Geochemical Modeling of Iron and Aluminum Precipitation during Mixing and Neutralization of Acid Mine Drainage Darrell Kirk Nordstrom U.S. Geological Survey, Boulder, CO 80303, USA; [email protected] Received: 21 May 2020; Accepted: 14 June 2020; Published: 17 June 2020 Abstract: Geochemical modeling of precipitation reactions in the complex matrix of acid mine drainage is fundamental to understanding natural attenuation, lime treatment, and treatment procedures that separate constituents for potential reuse or recycling. The three main dissolved constituents in acid mine drainage are iron, aluminum, and sulfate. During the neutralization of acid mine drainage (AMD) by mixing with clean tributaries or by titration with a base such as sodium hydroxide or slaked lime, Ca(OH)2, iron precipitates at pH values of 2–3 if oxidized and aluminum precipitates at pH values of 4–5 and both processes buffer the pH during precipitation. Mixing processes were simulated using the ion-association model in the PHREEQC code. The results are sensitive to the solubility product constant (Ksp) used for the precipitating phases. A field example with data on discharge and water composition of AMD before and after mixing along with massive precipitation of an aluminum phase is simulated and shows that there is an optimal Ksp to give the best fit to the measured data. Best fit is defined when the predicted water composition after mixing and precipitation matches most closely the measured water chemistry. Slight adjustment to the proportion of stream discharges does not give a better fit. Keywords: geochemical modeling; acid mine drainage; iron and aluminum precipitation; schwertmannite; basaluminite 1. -
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. -
Washington State Minerals Checklist
Division of Geology and Earth Resources MS 47007; Olympia, WA 98504-7007 Washington State 360-902-1450; 360-902-1785 fax E-mail: [email protected] Website: http://www.dnr.wa.gov/geology Minerals Checklist Note: Mineral names in parentheses are the preferred species names. Compiled by Raymond Lasmanis o Acanthite o Arsenopalladinite o Bustamite o Clinohumite o Enstatite o Harmotome o Actinolite o Arsenopyrite o Bytownite o Clinoptilolite o Epidesmine (Stilbite) o Hastingsite o Adularia o Arsenosulvanite (Plagioclase) o Clinozoisite o Epidote o Hausmannite (Orthoclase) o Arsenpolybasite o Cairngorm (Quartz) o Cobaltite o Epistilbite o Hedenbergite o Aegirine o Astrophyllite o Calamine o Cochromite o Epsomite o Hedleyite o Aenigmatite o Atacamite (Hemimorphite) o Coffinite o Erionite o Hematite o Aeschynite o Atokite o Calaverite o Columbite o Erythrite o Hemimorphite o Agardite-Y o Augite o Calciohilairite (Ferrocolumbite) o Euchroite o Hercynite o Agate (Quartz) o Aurostibite o Calcite, see also o Conichalcite o Euxenite o Hessite o Aguilarite o Austinite Manganocalcite o Connellite o Euxenite-Y o Heulandite o Aktashite o Onyx o Copiapite o o Autunite o Fairchildite Hexahydrite o Alabandite o Caledonite o Copper o o Awaruite o Famatinite Hibschite o Albite o Cancrinite o Copper-zinc o o Axinite group o Fayalite Hillebrandite o Algodonite o Carnelian (Quartz) o Coquandite o o Azurite o Feldspar group Hisingerite o Allanite o Cassiterite o Cordierite o o Barite o Ferberite Hongshiite o Allanite-Ce o Catapleiite o Corrensite o o Bastnäsite -
Rediscovery of the Elements — a Historical Sketch of the Discoveries
REDISCOVERY OF THE ELEMENTS — A HISTORICAL SKETCH OF THE DISCOVERIES TABLE OF CONTENTS incantations. The ancient Greeks were the first to Introduction ........................1 address the question of what these principles 1. The Ancients .....................3 might be. Water was the obvious basic 2. The Alchemists ...................9 essence, and Aristotle expanded the Greek 3. The Miners ......................14 philosophy to encompass a obscure mixture of 4. Lavoisier and Phlogiston ...........23 four elements — fire, earth, water, and air — 5. Halogens from Salts ...............30 as being responsible for the makeup of all 6. Humphry Davy and the Voltaic Pile ..35 materials of the earth. As late as 1777, scien- 7. Using Davy's Metals ..............41 tific texts embraced these four elements, even 8. Platinum and the Noble Metals ......46 though a over-whelming body of evidence 9. The Periodic Table ................52 pointed out many contradictions. It was taking 10. The Bunsen Burner Shows its Colors 57 thousands of years for mankind to evolve his 11. The Rare Earths .................61 thinking from Principles — which were 12. The Inert Gases .................68 ethereal notions describing the perceptions of 13. The Radioactive Elements .........73 this material world — to Elements — real, 14. Moseley and Atomic Numbers .....81 concrete basic stuff of this universe. 15. The Artificial Elements ...........85 The alchemists, who devoted untold Epilogue ..........................94 grueling hours to transmute metals into gold, Figs. 1-3. Mendeleev's Periodic Tables 95-97 believed that in addition to the four Aristo- Fig. 4. Brauner's 1902 Periodic Table ...98 telian elements, two principles gave rise to all Fig. 5. Periodic Table, 1925 ...........99 natural substances: mercury and sulfur. -
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. -
Koritnigite Zn(Aso3oh)•
Koritnigite Zn(AsO3OH) • H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Triclinic, pseudomonoclinic. Point Group: 1. As imperfect platy crystals, to 5 mm, in aggregates. Physical Properties: Cleavage: {010}, perfect; cleavage traces k [001] and k [100], visible on {010}. Tenacity: Flexible. Hardness = 2 D(meas.) = 3.54 D(calc.) = 3.56 Optical Properties: Transparent. Color: Colorless, white, rose. Luster: Pearly on {010}. Optical Class: Biaxial (+). Orientation: X = b; Y ∧ a ' 28◦; Z ∧ c ' 22◦. α = 1.632(5) β = 1.652(3) γ = 1.693(3) 2V(meas.) = 70(5)◦ Cell Data: Space Group: P 1. a = 7.948(2) b = 15.829(5) c = 6.668(2) α =90.86(2)◦ β =96.56(2)◦ γ =90.05(2)◦ Z=8 X-ray Powder Pattern: Tsumeb, Namibia; very close to cobaltkoritnigite. 7.90 (10), 3.16 (9), 3.83 (7), 2.461 (6), 2.186 (5), 3.95 (4), 2.926 (4) Chemistry: (1) (2) (3) As2O5 51.75 54.67 51.46 FeO + Fe2O3 trace 0.05 CoO 4.54 NiO 2.44 ZnO 35.97 25.83 36.44 MgO trace H2O [12.3] [12.47] 12.10 Total [100.0] [100.00] 100.00 2− (1) Tsumeb, Namibia; by electron microprobe, (AsO3OH) confirmed by IR, H2O by difference. • (2) J´achymov, Czech Republic; H2O by difference. (3) Zn(AsO3OH) H2O. Occurrence: A secondary mineral of the lower oxidation zone in a dolostone-hosted polymetallic hydrothermal ore deposit (Tsumeb, Namibia). Association: Tennantite, cuprian adamite, stranskiite, lavendulan, k¨ottigite,tsumcorite, prosperite, o’danielite (Tsumeb, Namibia); erythrite, arsenolite, sphalerite (J´achymov, Czech Republic). -
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. -
4Utpo3so UM-P-88/125
4utpo3So UM-P-88/125 The Incorporation of Transuranic Elements in Titanatc Nuclear Waste Ceramics by Hj. Matzke1, B.W. Seatonberry2, I.L.F. Ray1, H. Thiele1, H. Trisoglio1, C.T. Walker1, and T.J. White3'4'5 1 Commission of the European Communities, Joint Research Centre, i Karlsruhe Establishment, ' \ 'I European Institute for Transuranium Elements, Postfach 2340, D-7500 Karlsruhe, Federal Republic of Germany. 2 Advanced Materials Program, Australian Nuclear Science and Technology Organization, Private Mail Bag No. 1, Menai, N.S.W., 2234, Australia. 3 National Advanced Materials Analytical Centre, School of Physics, The University of Melbourne, Parkville, Vic, 3052, Australia. Supported by the Australian Natio-al Energy Research, Development and Demonstration Programme. 4 Member, The American Ceramic Society 5 Author to whom correspondence whould oe addressed 2 The incorporation of actinide elements and their rare earth element analogues in titanatc nuclear waste forms are reviewed. New partitioning data are presented for three waste forms contining Purex waste simulant in combination with either NpC^, PuC>2 or An^Oo. The greater proportion of transuranics partition between perovskitc and ztrconoiite, while some americium may enter loveringite. Autoradiography revealed clusters of plutonium atoms which have been interpreted as unrcacted dioxide or scsquioxide. It is concluded that the solid state behavior of transaranic elements in titanate waste forms is poorly understood; certainly inadequate to tailor a ceramic for the incorporation of fast breeder reactor wastes. A number of experiments are proposed that will provide an adequate, data base for the formulation and fabrication of transuranic-bearing jj [i waste forms. ' ' 1 ~> I. -
Aluminite Al2(SO4)(OH)4 • 7H2O C 2001-2005 Mineral Data Publishing, Version 1
Aluminite Al2(SO4)(OH)4 • 7H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. As needles and fibers, to 0.1 mm, commonly in reniform, nodular, or spherulitic masses, and as veinlets. Physical Properties: Fracture: Earthy, in aggregates. Tenacity: Friable. Hardness = 1–2 D(meas.) = 1.66–1.82 D(calc.) = 1.794 Optical Properties: Translucent, opaque if massive. Color: White to grayish white; colorless in transmitted light. Luster: Dull to earthy. Optical Class: Biaxial (+). Orientation: X = elongation. α = 1.459–1.460 β = 1.464 γ = 1.470 2V(meas.) = ∼90◦ Cell Data: Space Group: P 21/c. a = 7.440(1) b = 15.583(2) c = 11.700(2) β = 110.18(2)◦ Z=4 X-ray Powder Pattern: G´ant, Hungary. 7.93 (100), 9.01 (90), 3.7224 (72), 4.760 (71), 3.7419 (70), 5.033 (63), 4.868 (63) Chemistry: (1) (2) SO3 23.37 23.26 Al2O3 29.87 29.63 H2O 46.76 47.11 Total [100.00] 100.00 (1) Newhaven, England; recalculated to 100% after deduction of a small amount of gypsum. • (2) Al2(SO4)(OH)4 7H2O. Occurrence: Typically in clays or lignites, formed by the reaction of sulfate-bearing solutions from the decomposition of marcasite or pyrite at moderate temperatures with aluminous silicates; as a volcanic sublimate; in sulfur deposits; rarely in caves. Association: Basaluminite, gibbsite, epsomite, gypsum, celestine, dolomite, goethite. Distribution: In Germany, from Morl, near Halle, Saxony-Anhalt. In the Czech Republic, at Milevsko (M¨uhlhausen),near Kralupy, Kuchelbad, Miletic, and Velvary.