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An Application of Near-Infrared and Mid-Infrared Spectroscopy to the Study of 3 Selected Tellurite Minerals: Xocomecatlite, Tlapallite and Rodalquilarite 4 5 Ray L
QUT Digital Repository: http://eprints.qut.edu.au/ Frost, Ray L. and Keeffe, Eloise C. and Reddy, B. Jagannadha (2009) An application of near-infrared and mid- infrared spectroscopy to the study of selected tellurite minerals: xocomecatlite, tlapallite and rodalquilarite. Transition Metal Chemistry, 34(1). pp. 23-32. © Copyright 2009 Springer 1 2 An application of near-infrared and mid-infrared spectroscopy to the study of 3 selected tellurite minerals: xocomecatlite, tlapallite and rodalquilarite 4 5 Ray L. Frost, • B. Jagannadha Reddy, Eloise C. Keeffe 6 7 Inorganic Materials Research Program, School of Physical and Chemical Sciences, 8 Queensland University of Technology, GPO Box 2434, Brisbane Queensland 4001, 9 Australia. 10 11 Abstract 12 Near-infrared and mid-infrared spectra of three tellurite minerals have been 13 investigated. The structure and spectral properties of two copper bearing 14 xocomecatlite and tlapallite are compared with an iron bearing rodalquilarite mineral. 15 Two prominent bands observed at 9855 and 9015 cm-1 are 16 2 2 2 2 2+ 17 assigned to B1g → B2g and B1g → A1g transitions of Cu ion in xocomecatlite. 18 19 The cause of spectral distortion is the result of many cations of Ca, Pb, Cu and Zn the 20 in tlapallite mineral structure. Rodalquilarite is characterised by ferric ion absorption 21 in the range 12300-8800 cm-1. 22 Three water vibrational overtones are observed in xocomecatlite at 7140, 7075 23 and 6935 cm-1 where as in tlapallite bands are shifted to low wavenumbers at 7135, 24 7080 and 6830 cm-1. The complexity of rodalquilarite spectrum increases with more 25 number of overlapping bands in the near-infrared. -
Metamorphism of Sedimentary Manganese Deposits
Acta Mineralogica-Petrographica, Szeged, XX/2, 325—336, 1972. METAMORPHISM OF SEDIMENTARY MANGANESE DEPOSITS SUPRIYA ROY ABSTRACT: Metamorphosed sedimentary deposits of manganese occur extensively in India, Brazil, U. S. A., Australia, New Zealand, U. S. S. R., West and South West Africa, Madagascar and Japan. Different mineral-assemblages have been recorded from these deposits which may be classi- fied into oxide, carbonate, silicate and silicate-carbonate formations. The oxide formations are represented by lower oxides (braunite, bixbyite, hollandite, hausmannite, jacobsite, vredenburgite •etc.), the carbonate formations by rhodochrosite, kutnahorite, manganoan calcite etc., the silicate formations by spessartite, rhodonite, manganiferous amphiboles and pyroxenes, manganophyllite, piedmontite etc. and the silicate-carbonate formations by rhodochrosite, rhodonite, tephroite, spessartite etc. Pétrographie and phase-equilibia data indicate that the original bulk composition in the sediments, the reactions during metamorphism (contact and regional and the variations and effect of 02, C02, etc. with rise of temperature, control the mineralogy of the metamorphosed manga- nese formations. The general trend of formation and transformation of mineral phases in oxide, carbonate, silicate and silicate-carbonate formations during regional and contact metamorphism has, thus, been established. Sedimentary manganese formations, later modified by regional or contact metamorphism, have been reported from different parts of the world. The most important among such deposits occur in India, Brazil, U.S.A., U.S.S.R., Ghana, South and South West Africa, Madagascar, Australia, New Zealand, Great Britain, Japan etc. An attempt will be made to summarize the pertinent data on these metamorphosed sedimentary formations so as to establish the role of original bulk composition of the sediments, transformation and reaction of phases at ele- vated temperature and varying oxygen and carbon dioxide fugacities in determin- ing the mineral assemblages in these deposits. -
Speciation of Manganese in a Synthetic Recycling Slag Relevant for Lithium Recycling from Lithium-Ion Batteries
metals Article Speciation of Manganese in a Synthetic Recycling Slag Relevant for Lithium Recycling from Lithium-Ion Batteries Alena Wittkowski 1, Thomas Schirmer 2, Hao Qiu 3 , Daniel Goldmann 3 and Ursula E. A. Fittschen 1,* 1 Institute of Inorganic and Analytical Chemistry, Clausthal University of Technology, Arnold-Sommerfeld Str. 4, 38678 Clausthal-Zellerfeld, Germany; [email protected] 2 Department of Mineralogy, Geochemistry, Salt Deposits, Institute of Disposal Research, Clausthal University of Technology, Adolph-Roemer-Str. 2A, 38678 Clausthal-Zellerfeld, Germany; [email protected] 3 Department of Mineral and Waste Processing, Institute of Mineral and Waste Processing, Waste Disposal and Geomechanics, Clausthal University of Technology, Walther-Nernst-Str. 9, 38678 Clausthal-Zellerfeld, Germany; [email protected] (H.Q.); [email protected] (D.G.) * Correspondence: ursula.fi[email protected]; Tel.: +49-5323-722205 Abstract: Lithium aluminum oxide has previously been identified to be a suitable compound to recover lithium (Li) from Li-ion battery recycling slags. Its formation is hampered in the presence of high concentrations of manganese (9 wt.% MnO2). In this study, mock-up slags of the system Li2O-CaO-SiO2-Al2O3-MgO-MnOx with up to 17 mol% MnO2-content were prepared. The man- ganese (Mn)-bearing phases were characterized with inductively coupled plasma optical emission spectrometry (ICP-OES), X-ray diffraction (XRD), electron probe microanalysis (EPMA), and X-ray absorption near edge structure analysis (XANES). The XRD results confirm the decrease of LiAlO2 phases from Mn-poor slags (7 mol% MnO2) to Mn-rich slags (17 mol% MnO2). -
Mineral Processing
Mineral Processing Foundations of theory and practice of minerallurgy 1st English edition JAN DRZYMALA, C. Eng., Ph.D., D.Sc. Member of the Polish Mineral Processing Society Wroclaw University of Technology 2007 Translation: J. Drzymala, A. Swatek Reviewer: A. Luszczkiewicz Published as supplied by the author ©Copyright by Jan Drzymala, Wroclaw 2007 Computer typesetting: Danuta Szyszka Cover design: Danuta Szyszka Cover photo: Sebastian Bożek Oficyna Wydawnicza Politechniki Wrocławskiej Wybrzeze Wyspianskiego 27 50-370 Wroclaw Any part of this publication can be used in any form by any means provided that the usage is acknowledged by the citation: Drzymala, J., Mineral Processing, Foundations of theory and practice of minerallurgy, Oficyna Wydawnicza PWr., 2007, www.ig.pwr.wroc.pl/minproc ISBN 978-83-7493-362-9 Contents Introduction ....................................................................................................................9 Part I Introduction to mineral processing .....................................................................13 1. From the Big Bang to mineral processing................................................................14 1.1. The formation of matter ...................................................................................14 1.2. Elementary particles.........................................................................................16 1.3. Molecules .........................................................................................................18 1.4. Solids................................................................................................................19 -
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. -
Inis: Terminology Charts
IAEA-INIS-13A(Rev.0) XA0400071 INIS: TERMINOLOGY CHARTS agree INTERNATIONAL ATOMIC ENERGY AGENCY, VIENNA, AUGUST 1970 INISs TERMINOLOGY CHARTS TABLE OF CONTENTS FOREWORD ... ......... *.* 1 PREFACE 2 INTRODUCTION ... .... *a ... oo 3 LIST OF SUBJECT FIELDS REPRESENTED BY THE CHARTS ........ 5 GENERAL DESCRIPTOR INDEX ................ 9*999.9o.ooo .... 7 FOREWORD This document is one in a series of publications known as the INIS Reference Series. It is to be used in conjunction with the indexing manual 1) and the thesaurus 2) for the preparation of INIS input by national and regional centrea. The thesaurus and terminology charts in their first edition (Rev.0) were produced as the result of an agreement between the International Atomic Energy Agency (IAEA) and the European Atomic Energy Community (Euratom). Except for minor changesq the terminology and the interrela- tionships btween rms are those of the December 1969 edition of the Euratom Thesaurus 3) In all matters of subject indexing and ontrol, the IAEA followed the recommendations of Euratom for these charts. Credit and responsibility for the present version of these charts must go to Euratom. Suggestions for improvement from all interested parties. particularly those that are contributing to or utilizing the INIS magnetic-tape services are welcomed. These should be addressed to: The Thesaurus Speoialist/INIS Section Division of Scientific and Tohnioal Information International Atomic Energy Agency P.O. Box 590 A-1011 Vienna, Austria International Atomic Energy Agency Division of Sientific and Technical Information INIS Section June 1970 1) IAEA-INIS-12 (INIS: Manual for Indexing) 2) IAEA-INIS-13 (INIS: Thesaurus) 3) EURATOM Thesaurusq, Euratom Nuclear Documentation System. -
Thirty-Fourth List of New Mineral Names
MINERALOGICAL MAGAZINE, DECEMBER 1986, VOL. 50, PP. 741-61 Thirty-fourth list of new mineral names E. E. FEJER Department of Mineralogy, British Museum (Natural History), Cromwell Road, London SW7 5BD THE present list contains 181 entries. Of these 148 are Alacranite. V. I. Popova, V. A. Popov, A. Clark, valid species, most of which have been approved by the V. O. Polyakov, and S. E. Borisovskii, 1986. Zap. IMA Commission on New Minerals and Mineral Names, 115, 360. First found at Alacran, Pampa Larga, 17 are misspellings or erroneous transliterations, 9 are Chile by A. H. Clark in 1970 (rejected by IMA names published without IMA approval, 4 are variety because of insufficient data), then in 1980 at the names, 2 are spelling corrections, and one is a name applied to gem material. As in previous lists, contractions caldera of Uzon volcano, Kamchatka, USSR, as are used for the names of frequently cited journals and yellowish orange equant crystals up to 0.5 ram, other publications are abbreviated in italic. sometimes flattened on {100} with {100}, {111}, {ill}, and {110} faces, adamantine to greasy Abhurite. J. J. Matzko, H. T. Evans Jr., M. E. Mrose, lustre, poor {100} cleavage, brittle, H 1 Mono- and P. Aruscavage, 1985. C.M. 23, 233. At a clinic, P2/c, a 9.89(2), b 9.73(2), c 9.13(1) A, depth c.35 m, in an arm of the Red Sea, known as fl 101.84(5) ~ Z = 2; Dobs. 3.43(5), D~alr 3.43; Sharm Abhur, c.30 km north of Jiddah, Saudi reflectances and microhardness given. -
New Mineral Names*
AmericanMineralogM, Volume66, pages 1099-l103,IgEI NEW MINERAL NAMES* LouIs J. Cetnt, MrcHeer FtnrscHnn AND ADoLF Pnssr Aldermanlter Choloallte. I. R. Harrowficl4 E. R. Segnitand J. A. Watts (1981)Alderman- S. A. Williams (1981)Choloalite, CuPb(TeO3)z .HrO, a ncw min- ite, a ncw magnesiumalrrminum phosphate.Mineral. Mag.44, eral. Miaeral. Mag. 44, 55-51. 59-62. Choloalite was probably first found in Arabia, then at the Mina Aldermanite o@urs as minute, very thin" talc-likc crystallitcs La Oriental, Moctczuma, Sonora (the typc locality), and finally at with iuellite and other secondaryphosphates in the Moculta rock Tombstone, Arizona. Only thc Tombstone material provides para- phosphatc deposit near thc basc of Lower Cambrisn limestone genetic information. In this material choloalite occurs with cerus- close to Angaston, ca. 60 km NE of Adelaide. Microprobc analy- site, emmonsite and rodalquilarite in severcly brecciated shale that si.q supplcmented by gravimetric water determination gave MgO has been replaced by opal and granular jarosite. Wet chcmical E.4,CaO 1.2, AJ2O328.4, P2O5 25.9, H2O 36.1%,(totat 100),lead- analysisofcholoalitc from the type locality gave CuO 11.0,PbO ing to the formula Mg5Als2(POa)s(OH)zz.zH2O,where n = 32. 33.0,TeO2 50.7, H2O 3.4,total 98.1%,correspolding closcly to thc Thc powder diffraction pattern, taken with a Guinier camera, can formula in the titlc. Powder pattems of thc mineral from thc three be indexed on an orthorhombic. ccll with a = 15.000(7), D = localities can bc indexcd on the basis of a cubic ccll with a : 8.330(6),c - 26.60(l)A, Z = 2,D alc.2.15 from assumedcell con- l2.5l9A for the material from Mina La Oriental, Z: l2,D c,alc. -
JOURNAL the Russell Society
JOURNAL OF The Russell Society Volume 20, 2017 www.russellsoc.org JOURNAL OF THE RUSSELL SOCIETY The journal of British Isles topographical mineralogy EDITOR Dr Malcolm Southwood 7 Campbell Court, Warrandyte, Victoria 3113, Australia. ([email protected]) JOURNAL MANAGER Frank Ince 78 Leconfield Road, Loughborough, Leicestershire, LE11 3SQ. EDITORIAL BOARD R.E. Bevins, Cardiff, U.K. M.T. Price, OUMNH, Oxford, U.K. R.S.W. Braithwaite, Manchester, U.K. M.S. Rumsey, NHM, London, U.K. A. Dyer, Hoddlesden, Darwen, U.K. R.E. Starkey, Bromsgrove, U.K. N.J. Elton, St Austell, U.K. P.A. Williams, Kingswood, Australia. I.R. Plimer, Kensington Gardens, S. Australia. Aims and Scope: The Journal publishes refereed articles by both amateur and professional mineralogists dealing with all aspects of mineralogy relating to the British Isles. Contributions are welcome from both members and non-members of the Russell Society. Notes for contributors can be found at the back of this issue, on the Society website (www.russellsoc.org) or obtained from the Editor or Journal Manager. Subscription rates: The Journal is free to members of the Russell Society. The non-member subscription rates for this volume are: UK £13 (including P&P) and Overseas £15 (including P&P). Enquiries should be made to the Journal Manager at the above address. Back numbers of the Journal may also be ordered through the Journal Manager. The Russell Society: named after the eminent amateur mineralogist Sir Arthur Russell (1878–1964), is a society of amateur and professional mineralogists which encourages the study, recording and conservation of mineralogical sites and material. -
Clinocervantite, ~-Sb204, the Natural Monoclinic Polymorph of Cervantite from the Cetine Mine, Siena, Italy
Eur. J. Mineral. 1999,11,95-100 Clinocervantite, ~-Sb204, the natural monoclinic polymorph of cervantite from the Cetine mine, Siena, Italy RICCARDO BASSO 1, GABRIELLA LUCCHETTI I, LIVIa ZEFIRO 1 and ANDREA PALENZONA 2 IDipartimento di Scienze delia Terra dell'Universita, Corso Europa 26, 1-]6] 32 Genova, Ita]y e-mail: minera]@dister.unige.it 2Dipartimento di Chi mica e Chimica industria]e dell'Universita, Via Dodecaneso 3],1-]6]46 Genova, Ita]y Abstract: Clinocervantite occurs at the Cetine di Cotorniano mine associated with valentinite, tripuhyite, bindheimite and rosiaite. Clinocervantite, appearing generally as aggregates of single prisms elongated along [001] or twinned on {100}, is co]ourless, transparent, with vitreous lustre, biaxial, with the lowest measured ] ] refractive index a,' = .72 and the highest one y' = 2. O. The strongest lines in the powder pattern are dill = 3.244 A and d311 = 2.877 A. The crystal structure, space group C2Ie with a = 12.061(1) A, b = 4.836(1) A, ] e = 5.383( I) A, ~= 04.60( 4)" and Z = 4, has been refined to R = 0.020, confirming the new mineral to be the natural analogue of the synthetic ~-Sb204 already known. The structures of clinocervantite and cervantite may be regarded as built up by stacking layers of nearly identical structure and composition accounting for both polytypism in the Sb204 compound and twinning of the clinocervantite crystals. Key-words: clinocervantite, crystal-structure refinement, cervantite, twinning. Introduction Occurrence, physical properties and chemical composition During the study of rosiaite (Basso et al., 1996), an associated new mineral was found in materia] Clinocervantite occurs in litt]e cavities of a rock from the Cetine mine, central Tuscany, Italy. -
A Review of the Structural Architecture of Tellurium Oxycompounds
Mineralogical Magazine, May 2016, Vol. 80(3), pp. 415–545 REVIEW OPEN ACCESS A review of the structural architecture of tellurium oxycompounds 1 2,* 3 A. G. CHRISTY ,S.J.MILLS AND A. R. KAMPF 1 Research School of Earth Sciences and Department of Applied Mathematics, Research School of Physics and Engineering, Australian National University, Canberra, ACT 2601, Australia 2 Geosciences, Museum Victoria, GPO Box 666, Melbourne, Victoria 3001, Australia 3 Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, CA 90007, USA [Received 24 November 2015; Accepted 23 February 2016; Associate Editor: Mark Welch] ABSTRACT Relative to its extremely low abundance in the Earth’s crust, tellurium is the most mineralogically diverse chemical element, with over 160 mineral species known that contain essential Te, many of them with unique crystal structures. We review the crystal structures of 703 tellurium oxysalts for which good refinements exist, including 55 that are known to occur as minerals. The dataset is restricted to compounds where oxygen is the only ligand that is strongly bound to Te, but most of the Periodic Table is represented in the compounds that are reviewed. The dataset contains 375 structures that contain only Te4+ cations and 302 with only Te6+, with 26 of the compounds containing Te in both valence states. Te6+ was almost exclusively in rather regular octahedral coordination by oxygen ligands, with only two instances each of 4- and 5-coordination. Conversely, the lone-pair cation Te4+ displayed irregular coordination, with a broad range of coordination numbers and bond distances. -
Demesmaekerite Pb2cu5(UO2)2(Se O3)6(OH)6 • 2H2O C 2001-2005 Mineral Data Publishing, Version 1
4+ Demesmaekerite Pb2Cu5(UO2)2(Se O3)6(OH)6 • 2H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Triclinic. Point Group: 1. Crystals are elongated along [001] and flattened on {100} or {010}, with dominant {100} and {010}, secondary faces typically striated k [101], to 1 cm; in radial aggregates. Physical Properties: Hardness = 3–4 D(meas.) = 5.28(4) D(calc.) = 5.42 Radioactive. Optical Properties: Translucent to opaque. Color: Bottle-green to pale olive-green, becoming brownish green with dehydration. Optical Class: Biaxial (+). Pleochroism: X 0 = yellow-green; Y 0 = brown. α = 1.835(5) (α 0) β = n.d. γ = 1.910(5) (γ 0) 2V(meas.) = n.d. Cell Data: Space Group: P 1. a = 11.955(5) b = 10.039(4) c = 5.639(2) α =89.78(4)◦ β = 100.36(4)◦ γ =91.34(4)◦ Z=1 X-ray Powder Pattern: Musonoi mine, Congo. 2.97 (FFF), 5.42 (FF), 5.89 (F), 3.34 (F), 5.14 (mF), 4.72 (mF), 4.67 (mF) Chemistry: (1) (2) SeO2 30.9 30.65 UO3 27.6 26.34 PbO 19.4 20.55 CuO 18.2 18.31 H2O 4.2 4.15 Total 100.3 100.00 (1) Musonoi mine, Congo; H2O by the Penfield method; corresponds to Pb1.87Cu4.93(UO2)2.08 • • (SeO3)6(OH)6.04 2H2O. (2) Pb2Cu5(UO2)2(SeO3)6(OH)6 2H2O. Occurrence: Rare in the lower oxidized portions of a selenium-bearing Cu–Co deposit. Association: Cuprosklodowskite, kasolite, guilleminite, derriksite, chalcomenite, malachite, selenian digenite.