Follow up the Leaching Efficiency of Uranium Series from High-Grade Granite Sample with High Concentration of Sulfuric Acid

Total Page:16

File Type:pdf, Size:1020Kb

Follow up the Leaching Efficiency of Uranium Series from High-Grade Granite Sample with High Concentration of Sulfuric Acid PROCEEDINGS: Nada et al. Follow up the leaching efficiency of uranium series from high-grade granite sample with high concentration of sulfuric acid A. Nada1, N. Imam2*, A. Ghanem1 1 Physics Department, Faculty of Women for Art, Science and Education, Ain Shams University, 11757, Egypt. 2 National Institute of Oceanography and Fisheries, Cairo, 11516, Egypt Keywords: Leaching efficiency, Granite sample, Sulfuric acid Presenting author, e-mail: [email protected] Introduction Materials and methods Uranium is the most representative actinide element that Sample preparation is of fundamental importance in the nuclear fuel cycle. The red granite sample from Gabal Gattar, the Northern Uranium is a naturally occurring radionuclide which has Eastern Desert (2352.8 ppm), was crushed and grinded 238 9 235 three isotopes ( U (t1/2=4.5x10 yr) 99.72 %, U into 63 mesh and then quartered to obtain representative 8 234 5 (t1/2=7.1x10 yr) 0.0055 % and U (t1/2=2.5x10 yr) sample. The mineralogical characterization of the granite 0.72 %. It has several oxidation states tetravalent and sample was done using X-Ray Diffraction (XRD) (Model hexavalent which dominant in the environment. D8 discover manufacture by USA). The sample is Hexavalent uranium is more dissoluble and mobile than measured by y-spectrometry, using an HPGe-detector to tetravalent uranium. Extraction of uranium is indeed determine the activity concentrations (Bq) of Uranium a hydrometallurgical operation in which uranium is isotopes (238U, 235U, and 234U), 230Th and 226Ra series. The directly leached first by suitable acid or alkaline reagents conditions of the leaching procedures were 50 g of sample, (Kraiz et al., 2016). Acid leaching is more widely used 98 % (H2SO4) acid concentration, 60 min stirring time, 1:3 than the alkaline one because of relatively coarse solid/liquid ratios at room temperature. The leaching preparatory grinding, comparatively mild reagent procedures performed with two methods to determine the concentration, shorter leaching times, applied under an leaching efficiency. After the leaching process, the ambient temperature and atmospheric pressure, the sample was filtered by using filter paper to get pregnant highest extraction efficiency, convenient for subsequent solution and the second method the sample without filter recovery processes (Kraiz et al., 2016; Nada et al., 2019). to get solution named total sample. Leaching mining is a new type of deposit mining technology that includes a solid liquid transfer process Analytical techniques transmitting useful elements from the ore to the leaching The leachate (pregnant solution) and total solution were solution. measured by an HPGe detector at interval time for more The granitic rocks constitute about 60% of the total than four months. The detector has a relative efficiency of neoproterozoic outcrops of the Eastern Desert of Egypt. about 50 % of the 3"x3" Nal(Tl) crystal efficiency, (El Gaby, 1975) classified the granites in Egypt into two connected to multichannel analyzer card (MCA) installed groups: (a) synorogenic granitoids, and (b) younger in a PC computer. The software program MAESTRO-32 granites, which include the post-orogenic pink and red was used to accumulate and analyze the data. The system granites. The younger granites of the Northern Eastern was calibrated for energy to display gamma photo peaks Desert found to be favourable for uranium mineralization between 63 and 3000 keV. The efficiency calibration was and showed significantly higher level of radioactivity performed by using three well-known reference materials (Kraiz et al., 2016). Gabal Gattar area was located at obtained from the International Atomic Energy Agency Eastern Desert, the west of Hurghada city at the Red Sea for U, Th and K activity measurements: RGU-1, RGTh- coast. The younger granites of G. Gattar are highly 1and RGK-1 (IAEA, 1987). Uranium-238 activity was fractured, sheared and subjected to hydrothermal determined in directly from the gamma rays emitted by its alteration processes. The U-mineralization at this daughter product 234mPa whose activity was determined occurrence are mainly related to presence of some from 1001 keV photo peaks (Sutherland and deJong, uranium minerals such as uraninite, pitchblende, 1990). The uranium-235 activity was determined directly uranophane, beta uranophane, clarkeite, zippeite, soddyite by its gamma ray peaks; 143.8, 163.4, 185.7, and 205.3 and kosolite as well as some U-bearing accessory and keV (Yucel et al., 1998). The 234U activity was determined secondary minerals like zircon, sphene, chlorite, fluorite from the gamma rays emitted from this nuclide at energies and iron-uraniferous grains (El-Galy et al., 2007). The of 53.2 keV and 120.9 keV (Yokoyama et al., 2008). main objective of the present investigation is studying Thorium-230 was determined from the 67.7 keV peak uranium leaching efficiency of granite sample with high (Simpson, and Grtin, 1998). The specific activity of 226Ra concentration of acid. In this type of study, Laboratory was measured using the186.1 keV from its own gamma- tests are used to evaluate a heap leach process using a ray (after the subtraction of the185.7 keV of 235U). The batch type of testing methodology. We attempt to follow specific activity of 214Pb was measured using the 241.9, up the leaching efficiency of uranium isotopes from high- 295.2keVand 351.9 keV while the specific activity of grade granite sample with high concentration of sulfuric 214Bi was measured using the 609.3keV. The activity acid at different interval time. concentrations of these radionuclides were measured by using the relation given in equation (1) (Bakr, 2014). 60 PROCEEDINGS: Nada et al. (1) Results and discussion where: Chemical analysis of Gabal Gattar granite sample Ai is the activity concentration of radionuclide (i) in The mineralogical composition of the granite sample has Bq kg-1, a good source for the alkali oxides (K2O + Na2O) B.RY is the emission probability of the gamma line contained in potash feldspar minerals (orthoclase and corresponding to the peak energy (Y) of radionuclide (i), microcline) and the sodic plagioclase feldspar mineral is the spectrometer's efficiency corresponding to the (albite) as shown in Table 1 and Figure 1. The chemical peak energy (Y) at the specific geometry, analysis of granite sample presented the major oxides of NsY is the net count under the peak area of the selected the sample Table 2. Oxygen and SiO2 were the main major gamma line for the measured sample, oxide of the studied sample and Al2O3 was the second t is the real counting time, and major oxide. The studied red younger granite M is the mass of the sample in kg. characterized enrichment in alkalis (K2O+Na2O) and The leaching efficiency of the radionuclides was albite. calculated according to the following equation: Leaching efficiency (%) = Activity concentration in leachate (Bq) / Activity concentration in the original sample (Bq) (2) I All.I Ca0.1 K0.27 Na0.63 08 Si2.9J\northodase ~ I Al K 08 SiJ Sankline t 02S! Quartzlow ~ I ~ . 8 1 ◄ Ca0 . 32 N a 0.1&O ◄ Sl1 , 1 84L a b4'tdoflte f AINa08Si3Albile I Al K0.89 Na0.11 08 Si3 MIClodine ~ I U i ~ 8 i I i ~~ . ) i ,,1•• ~•/1.. ~,-, ~ p, •> 1,, I 30 -~~~40 50 ! 60 70 80 " 20 2Thela (Coupled Twolhala/Theta) WL0 1.54060 Figure 1. The XRD diffraction pattern of granite sample. Table 1. The mineralogical characterization of G.Gattar granite sample. Compound Quartz Orthoclase Albite Microcline U Th Name low Wt (%) I 43.6 I 29.5 I 23.6 I 0.5 11 2.7 I 0.1 I Table 2. Chemical compositions of G.Gattar granite sample. Chemical Oxygen Na2O Al2O3 SiO2 K2O CaO UO2 ThO2 composition Wt (%) I 47.5 I 5.2 I 10.1 I 31.1 I 4.7 I 0.7 I 0.5 I 0.1 I Radiometric measurement context, 226Ra series has little changed from start point The activity concentrations of solid, leaching and total into 20 days and after that nearly slightly constant. This sample are shown in Table 3. In solid sample, there was may due to lower solubility of these radionuclides. From secular equilibrium between 238U and 226Ra and Figure (2, 3), it's obvious that, 230Th has highest activity disequilibrium with 234U that has the highest activity concentration which may be due to alpha recoil (Shiobara concentration. The sample indicated that preferential et al., 2017) and the solubility of 230Th increases in acidic abundance of 234U relative to 238U may due to prevailing aqueous solutions (Abdelouas, 2006). reducing conditions. The ARs of 234U/238U were higher than unity little In leaching sample, the activity concentration of 238U, changing from start until end of time as shown in Figure 230Th and 235U started increasing from start point into 4. This may be due to preferential release of 234U from 40 days and after that became slightly constant. On the damaged lattice sites produced bya-recoil atoms of 234U other hand, 234U has narrow change from start point to end during the leaching period (Bonotto et al., 2001; Andersen of time; we can say no change with the time. This may et al., 2009). However, due to different oxidation states, due to hexavalent uranium is more mobile at higher 234U forms more soluble U (VI) complexes and remains acidity, and tetravalent uranium will oxidize and convert in solution, while 238U present in the form of less soluble into hexavalent uranium. The 234U on the surface of the U (IV) complexes, precipitates (Pekala et al., 2010). The granite sample was dissolved quickly the leaching ARs of 230Th/238U were higher than unity started closed solution increased rapidly to its maximum. On the same into unity and increased with the time.
Recommended publications
  • 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.
    [Show full text]
  • United States Department of the Interior Geological Survey
    UNITED STATES DEPARTMENT OF THE INTERIOR GEOLOGICAL SURVEY A CATALOG OF STUDY MATERIAL OF RADIOACTIVE MINERALS T. W. Stern October 1950 Trace Elements Investigations Report 129 JAN 1 0 2081' CONTENTS Page Introduction ......................... Group A. Uranium and thorium minerals Group B. Minerals with minor amounts of uranium and thorium ................................ 62 Group C. Synthetic uranium compounds pre­ pared by the U. S. Geological Survey ............... ^9 A CATALOG OF STUDY MATERIAL OF RADIOACTIVE MINERALS by T. W. Stern Introduction This catalog is a list of specimens of radioactive minerals for which the Geological Survey has been collecting optical, X-ray dif­ fraction, and other data. The specimens are in the study collections of the U. S. National Museum, the Mineralogical Museum of Harvard University (including some specimens on loan at Harvard from the American Museum of Natural History), and the Geological Survey. The listing does not include all specimens in these institutions, but it does include those specimens for which X-ray patterns can be made available as well as representative specimens from significant local­ ities. In addition, references are given to material on deposit, at the U. S. National Museum, that has been described in the literature. Because of the rarity of much of the material here listed, re­ quests for study material must be considered individually. Regardless of the quantity of material, any request granted by the U. S. National Museum will have to be accepted on the terms laid down by that organ­ ization to conserve limited or rare minerals. Those minerals that show external crystal form but do not give X-ray powder diffraction patterns are listed with the word "ignited" after the X-ray powder diffraction photograph number.
    [Show full text]
  • Thn Auertcan M Rlueralocrsr
    THn AUERTcANM rluERALocrsr JOURNAL OF TIIE MINDRALOGICAL SOCIETY OF ANIERICA vbl.41 JULY-AUGUST, 1956 Nos. 7 and 8 MTNERAL COMPOSTTTON OF G'UMMTTE*f Crrllonl FnoNonr, H artard Llniaersity,Cambrid,ge, M ass., and. U. S. GeologicalSurwy, Washington, D.C. ABSTRACT The name gummite has been wideiy used for more than 100 years as a generic term to designate fine-grained yellow to orange-red alteration products of uraninite whose true identity is unknown. A study of about 100 specimens of gummite from world-wide localities has been made by r-ray, optical, and chemical methods. rt proved possible to identify almost all of the specimens with already known uranium minerals. Gummite typicalty occurs as an alteration product of uraninite crystals in pegmatite. Such specimensshow a characteristic sequenceof alteration products: (1) A central core of black or brownish-black uraninite. (2) A surrounding zone, yellow to orange-red, composed chiefly of hydrated lead uranyl oxides. This zone constitutes the traditional gummite. It is principally composed of fourmarierite, vandendriesscheite and two unidentified phases (Mineral -4 and Mineral c). Less common constituents are clarkeite, becquerelite, curite, and schoepite. (3) An outer silicate zone. This usually is dense with a greenish-yellow color and is composed of uranophane or beta-uranophane; it is sometimes soft and earthy with a straw-yellow to pale-brown color and is then usually composed of kasolite or an unidenti- fied phase (Minerat B). Soddyite and sklodowskite occur rarely. There are minor variations in the above general sequence. rt some specimens the core may be orange-red gummite without residual uraninite or the original uraninite crystal may be wholly converted to silicates.
    [Show full text]
  • SIMPLE URANIUM OXIDES, HYDROXIDES U4+ + U6+, SIMPLE and COMPLEX URANYL HYDROXIDES in ORES Andrey A
    New Data on Minerals. 2011. Vol. 46 71 SIMPLE URANIUM OXIDES, HYDROXIDES U4+ + U6+, SIMPLE AND COMPLEX URANYL HYDROXIDES IN ORES Andrey A. Chernikov Fersman Mineralogical Museum, Russian Academy of Sciences, Moscow, [email protected], [email protected] The review of published and new own data of simple uranium oxides revealed that the formation of five simple oxides is probable: nasturan, sooty pitchblende, uraninite, uranothorianite, and cerianite. Among simple oxides, nasturan, sooty pitchblende, and uraninite are the most abundant in ores varied in genesis and mineralogy. Uranothorianite or thorium uraninite (aldanite) is occasional in the ores, while cerianite is believed in U-P deposits of Northern Kazakhstan. Hydrated nasturan is the most abundant among three uranium (IV+VI) hydroxides in uranium ores. Insignificant ianthinite was found in few deposits, whereas cleusonite was indentified only in one deposit. Simple uranyl hydroxides, schoepite, metaschoepite, and paraschoepite, are widespread in the oxidized ores of the near-surface part of the Schinkolobwe deposit. They are less frequent at the deeper levels and other deposits. Studtite and metastudtite are of insignificant industrial importance, but are of great inter- est to establish genesis of mineral assemblages in which they are observed, because they are typical of strongly oxidized conditions of formation of mineral assemblages and ores. The X-ray amorphous urhite associated with hydrated nasturan and the X-ray amorphous hydrated matter containing ferric iron and U6+ described for the first time at the Lastochka deposit, Khabarovsk krai, Russia are sufficiently abundant uranyl hydroxides in the oxidized uranium ores. Significant complex uranyl hydroxides with interlayer K, Na, Ca, Ba, Cu, Pb, and Bi were found basically at a few deposits: Schinkolobwe, Margnac, Wölsendorf, Sernyi, and Tulukuevo, and are less frequent at the other deposits, where quite large monomineralic segregations of nasturan and crystals of uraninite were identified.
    [Show full text]
  • Clarkeite (Na, Ca, Pb)(UO2)O(OH) • 0−1H2O C 2001-2005 Mineral Data Publishing, Version 1
    Clarkeite (Na, Ca, Pb)(UO2)O(OH) • 0−1H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Hexagonal. Point Group: 32/m. As dense microcrystalline replacements of uraninite, which may be mineralogically zoned. Physical Properties: Fracture: Conchoidal to splintery. Tenacity: Brittle. Hardness = 4–4.5 D(meas.) = 6.29–6.39 D(calc.) = 6.74 Radioactive. Optical Properties: Opaque, transparent in thin grains. Color: Dark brown, mahogany- brown, chocolate-brown, or reddish orange; reddish brown to orange-brown or orange in transmitted light. Streak: Yellowish brown. Luster: Slightly waxy. Optical Class: Biaxial (–). Pleochroism: Weak; in darker oranges. Dispersion: r< v,weak. α = 1.997 β = 2.098 γ = 2.108 2V(meas.) = 30◦–50◦ Cell Data: Space Group: R3m. a = 3.954(1) c = 17.660(3) Z = 3 X-ray Powder Pattern: Fanny Gouge mine, North Carolina, USA. 3.195 (100), 5.903 (64), 3.365 (56), 2.707 (34), 1.9772 (33), 2.945 (28), 1.6410 (23) Chemistry: (1) (2) (3) (1) (2) (3) UO3 81.72 79.9 83.14 MgO 0.28 SiO2 0.50 0.03 CaO 2.84 2.1 0.37 UO2 0.8 SrO 0.29 ThO2 2.4 0.49 Na2O 3.44 2.3 7.01 Al2O3 0.92 K2O 0.48 0.42 + Y2O3 0.82 H2O 3.36 4.2 − RE2O3 2.62 H2O 1.3 Fe2O3 0.18 H2O [3.47] PbO 3.71 7.9 3.96 insol. 0.14 0.2 Total 100.19 101.1 [100.00] (1) Spruce Pine, North Carolina, USA.
    [Show full text]
  • STRONG and WEAK INTERLAYER INTERACTIONS of TWO-DIMENSIONAL MATERIALS and THEIR ASSEMBLIES Tyler William Farnsworth a Dissertati
    STRONG AND WEAK INTERLAYER INTERACTIONS OF TWO-DIMENSIONAL MATERIALS AND THEIR ASSEMBLIES Tyler William Farnsworth A dissertation submitted to the faculty at the University of North Carolina at Chapel Hill in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry. Chapel Hill 2018 Approved by: Scott C. Warren James F. Cahoon Wei You Joanna M. Atkin Matthew K. Brennaman © 2018 Tyler William Farnsworth ALL RIGHTS RESERVED ii ABSTRACT Tyler William Farnsworth: Strong and weak interlayer interactions of two-dimensional materials and their assemblies (Under the direction of Scott C. Warren) The ability to control the properties of a macroscopic material through systematic modification of its component parts is a central theme in materials science. This concept is exemplified by the assembly of quantum dots into 3D solids, but the application of similar design principles to other quantum-confined systems, namely 2D materials, remains largely unexplored. Here I demonstrate that solution-processed 2D semiconductors retain their quantum-confined properties even when assembled into electrically conductive, thick films. Structural investigations show how this behavior is caused by turbostratic disorder and interlayer adsorbates, which weaken interlayer interactions and allow access to a quantum- confined but electronically coupled state. I generalize these findings to use a variety of 2D building blocks to create electrically conductive 3D solids with virtually any band gap. I next introduce a strategy for discovering new 2D materials. Previous efforts to identify novel 2D materials were limited to van der Waals layered materials, but I demonstrate that layered crystals with strong interlayer interactions can be exfoliated into few-layer or monolayer materials.
    [Show full text]
  • Clarkeite: New Chemical and Structural Data
    American Mineralogist, Volume 82, pages 607±619, 1997 Clarkeite: New chemical and structural data ROBERT J. FINCH* AND RODNEY C. EWING Department of Earth and Planetary Sciences, University of New Mexico, Albuquerque, New Mexico 87131, U.S.A. ABSTRACT Clarkeite crystallizes during metasomatic replacement of pegmatitic uraninite by late- stage, oxidizing hydrothermal ¯uids. Samples are zoned compositionally: Clarkeite, which is Na rich, surrounds a K-rich core (commonly with remnant uraninite) and is surrounded by more Ca-rich material; volumetrically, clarkeite is most abundant. Clarkeite is hexag- onal (space group Rm3Å )a53.954(4), c 5 17.73(1) AÊ (Z 5 3). The structure of clarkeite is based on anionic sheets of the form [(UO2)(O,OH)2]. The sheets are bonded to each other through interlayer cations and H2O molecules. The empirical formula for clarkeite from the Fanny Gouge mine near Spruce Pine, North Carolina, is: {Na0.733K0.029Ca0.021Sr0.009Y0.024Th0.006Pb0.058}S0.880[(UO2)0.942O0.918(OH)1.082](H2O)0.069. Na predominates and the Pb is radiogenic. The general formula for clarkeite is 21 31 41 {(Na,K)pMMMPbqr s x}[(UO2)1 2 xO1 2 y(OH)1 1 y](H2O)z where Na .. K and p . (q 1 r 1 s). The number of O22 ions and OH groups in the structural unit is determined by the net charge of the interlayer cations (except Pb): y 5 1 2 (p 1 2q 1 3r 1 4s). This suggests that the ideal formula for ideal end-member clarkeite is Na[(UO2)O(OH)](H2O)0-1.
    [Show full text]
  • The Pegmatite Dyke at Rømteland
    The pegmatite dyke at Rømteland. A c/e^ci/ii/on of the mme^a/F and a ck/FcuFFlon of the mineral paragenesis, especially within the system (Fe, Mn)O-TiO2-Y2O3-(Nb, Ta)205-Si02 By Thor L. Sverdrup Contents lntro^uction 125 Magnetite 161 125 162 Description of the area 127 162 6etelM!NstionB 128 163 History 129 Orangite 163 Description of the pegmatite .... 130 Palygorskite 164 Temperature of formation of the Plagioclase 164 pegmatite 134 p^rite 166 Magmatic origin; supporting Quartz 166 odBervation3 142 3amalBliite 167 OeBci'lption ot tlie mineral 143 Spessartite 168 143 3pkene 169 147 169 153 170 Apatite 156 170 Bastnåsite 156 Uraninite 170 Lei-yl 157 Clarkeite 171 Liotite 157 171 Oalcite 158 l<2B3olite 171 Chalcopyrite 158 a-uranophane 171 158 ?ircon 171 Chlorite (Daphnite) 158 Mineral paragenesis at Rømteland 173 Columbite 158 The two adjacent four component 159 system with the oxides: (Fe, Luxenite 159 Mn)O-Y2O3-(Nb, Ta)2O5-TiOé> ?luolite 160 SiO2 181 Nematite 160 161 Sammendrag 191 Ilmenite 161 195 Introduction. The pegmatite described is located at Rømteland, about 7 km W of Vigeland, Vest-Agder county, southern Norway. Field investigations were made in the summers of 1955 and 1956, and v the laboratory work was done under the direction of Professor Dr. Tom F. W. Barth and Dr. H. Neumann. The pe^matite is BUllouncie6 by a hornblende bearing quartz monzonite which Barth (1945) has called farsundite. Major (1939) believes the quartz monzonite to be a magmatic rock which during its emplacement has torn loose pieces of the sur rounding gneiss and partly assimilated these.
    [Show full text]
  • Complete Title of My Thesis
    GEOCHEMISTRY OF URANIUM AT MINERAL-WATER INTERFACES: RATES OF SORPTION-DESORPTION AND DISSOLUTION-PRECIPITATION REACTIONS Thesis by Daniel Giammar In Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy California Institute of Technology Pasadena, California 2001 (Defended May 8, 2001) ii © 2001 Daniel Giammar All Rights Reserved iii Acknowledgments My advisor Janet Hering has supported and encouraged me throughout my graduate student career. From her I have learned a great deal about aquatic chemistry and, by her example, much about scientific curiosity and discipline. She is consistently my best and most thorough critic. Michael Hoffmann’s encouragement and suggestions have contributed in many ways to my work. George Rossman’s mineralogical insight led to some of the most interesting experiments in this work. Jim Morgan has been a mentor and role model throughout my study at Caltech, and I would particularly like to thank him for his emphasis on the fundamentals, both scientifically and on the basketball court. I would like to acknowledge the profound influence that Susan Leach, my middle school life and earth sciences teacher, had on my decision to pursue a career in environmental science and engineering. David Dzombak at Carnegie Mellon encouraged me to go to graduate school and remains a great role model for me. At Caltech, Gerald Wasserburg’s enthusiasm for geochemistry got me interested in uranium and his encouragement contributed to the initiation of this work. The summer undergraduate research projects of Helen Claudio and Yi-Ping Liu constitute portions of this work. When I would run into a problem with the X-ray diffractometer or scanning electron microscope, Chi Ma was always there to bail me out.
    [Show full text]
  • Attachment SOTERM)
    Title 40 CFR Part 191 Subparts B and C Compliance Recertification Application for the Waste Isolation Pilot Plant Appendix SOTERM-2009 Actinide Chemistry Source Term United States Department of Energy Waste Isolation Pilot Plant Carlsbad Field Office Carlsbad, New Mexico Appendix SOTERM-2009 Actinide Chemistry Source Term Title 40 CFR Part 191 Subparts B and C Compliance Recertification Application 2009 Table of Contents SOTERM-1.0 Introduction ............................................................................................SOTERM-1 SOTERM-2.0 Expected WIPP Repository Conditions, Chemistry, and Processes ......SOTERM-3 SOTERM-2.1 Ambient Geochemical Conditions .....................................................SOTERM-3 SOTERM-2.2 Repository Conditions........................................................................SOTERM-3 SOTERM-2.2.1 Repository Pressure.....................................................................SOTERM-5 SOTERM-2.2.2 Repository Temperature..............................................................SOTERM-5 SOTERM-2.2.3 Water Content and Relative Humidity ........................................SOTERM-5 SOTERM-2.2.4 Minimum Repository Brine Volume...........................................SOTERM-6 SOTERM-2.2.5 DRZ.............................................................................................SOTERM-7 SOTERM-2.3 Repository Chemistry.........................................................................SOTERM-7 SOTERM-2.3.1 WIPP Brine..................................................................................SOTERM-7
    [Show full text]
  • Minerals Localities
    MINERALS and their LOCALITIES This book is respectfully dedicated to the memory of Dr. John Sinkankas for his kind initiative and support to publish this book in English version. MINERALS and their LOCALITIES Jan H. Bernard and Jaroslav Hyršl Edited by Vandall T. King © 2004 by Granit, s.r.o. © 2004 Text by Jan H. Bernard and Jaroslav Hyršl © 2004 Photos by Jaroslav Hyršl (463), Studio Granit (534), Jaromír Tvrdý (34), Petr Zajíček (4) The photographed specimens are from the collections of both authors as well as from many other collections. The autors are grateful to all institutions and persons who allowed to photograph their specimens for this book. Front cover photos: Turquoise, polished, 55 mm, Zhilandy, Kazakhstan, G Galena, 45 mm, Madan, Bulgaria, G Sphalerite, xx 12 mm, Morococha, Peru, H Gypsum, xx 40 mm, Las Salinas, Peru, H Variscite, xx 5 mm, Itumbiara, Brazil, H Rhodochrosite, polished, 50 mm, Capillitas, Argentina, H Back cover photo: Wolframite, 45 mm, Yaogangxian, China, H Page 1: Muscovite, 45 mm, Linopolis, Brazil, H Page 2: Vivianite, 100 mm, Huanzala, Bolivia, H Page 3: Liddicoatite, polished, 70 mm, Anjanabonoina, Madagaskar, G Page 5: Opal - fire, polished, 50 mm, Mezezo, Ethiopia, G Page 12: Brazilianite, 35 mm, Linopolis, Brazil, H Page 13: Gold, 35 mm, Eagle's Nest Mine, California, G Published by Granit, s.r.o. Štefánikova 43, 150 00 Praha 5, Czech Republic e-mail: [email protected] www.granit-publishing.cz Composition and reproduction by Studio VVG, Prague Printed in Czech Republic by Finidr, s.r.o., Český Těšín 14/02/03/01 All rights reserved.
    [Show full text]
  • Rutherfordine U O2(CO3) C 2001-2005 Mineral Data Publishing, Version 1
    6+ Rutherfordine U O2(CO3) c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Orthorhombic. Point Group: mm2. Crystals are lathlike, elongated along [001], with large {100}, {010}, {001}, to 3 mm; commonly radiating, fibrous, matted, in pulverulent, earthy to very fine-grained dense masses. Physical Properties: Cleavage: On {010}, perfect; on {001}, less perfect. Hardness = n.d. D(meas.) = 5.7 D(calc.) = 5.682 Radioactive. Optical Properties: Semitransparent. Color: Pale yellow, straw-yellow, greenish yellow, orange, amber-brown, may be zoned. Luster: Dull to earthy, silky if fibrous. Optical Class: Biaxial (+). Pleochroism: Slight; X = colorless; Y = pale yellow; Z = pale greenish yellow. Orientation: X = b; Y = c; Z = a. α = 1.715–1.723 β = 1.728–1.730 γ = 1.755–1.795 2V(meas.) = Large. 2V(calc.) = 53◦ Cell Data: Space Group: Imm2. a = 4.840(1) b = 9.273(2) c = 4.298(1) Z = 2 X-ray Powder Pattern: Uluguru Mountains, Tanzania. 4.61 (100), 4.30 (70), 3.23 (40), 3.92 (30), 2.64 (25), 2.309 (20), 2.062 (20) Chemistry: (1) (2) (3) CO2 13.1 13.6 13.33 UO3 86.7 86.6 86.67 + H2O 0.2 Total [100.0] 100.2 100.00 (1) Uluguru Mountains, Tanzania; recalculated to 100% from an original total of 100.3%, after deduction of Pb and Ca as kasolite and uranophane, and remaining FeO and CaO as impurities. (2) Katanga Province, Congo. (3) UO2(CO3). Occurrence: A secondary mineral formed as a weathering product of uraninite. Association: Uraninite, becquerelite, masuyite, schoepite, kasolite, curite, boltwoodite, vandendriesscheite, billietite, metatorbernite, fourmarierite, studtite, sklodowskite.
    [Show full text]