The Pyrochlore Supergroup of Minerals: Nomenclature
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Geochemical Alteration of Pyrochlore Group Minerals: Pyrochlore Subgroup
American Mineralogist, Volume 80, pages 732-743, 1995 Geochemical alteration of pyrochlore group minerals: Pyrochlore subgroup GREGORY R. LUMPKIN Advanced Materials Program, Australian Nuclear Science and Technology Organization, Menai 2234, New South Wales, Australia RODNEY C. EWING Department of Earth and Planetary Sciences, University of New Mexico, Albuquerque, New Mexico 87131, U.S.A. ABSTRACT Primary alteration of uranpyrochlore from granitic pegmatites is characterized by the substitutions ADYD-+ ACaYO, ANaYF -+ ACaYO, and ANaYOI-I --+ ACaYO. Alteration oc- curred at ""450-650 °C and 2-4 kbar with fluid-phase compositions characterized by relatively low aNa+,high aeaH, and high pH. In contrast, primary alteration of pyrochlore from nepheline syenites and carbonatites follows a different tre:nd represented by the sub- stitutions ANaYF -+ ADYD and ACaYO -+ ADYD. In carbonatites, primary alteration of pyrochlore probably took place during and after replacement of diopside + forsterite + calcite by tremolite + dolomite :t ankerite at ""300-550 °C and 0-2 kbar under conditions of relatively low aHF, low aNa+,low aeaH, low pH, and elevated activities of Fe and Sr. Microscopic observations suggest that some altered pyrochlor1es are transitional between primary and secondary alteration. Alteration paths for these specimens scatter around the trend ANaYF -+ ADYD. Alteration probably occurred at 200-350 °C in the presence of a fluid phase similar in composition to the fluid present during primary alteration but with elevated activities of Ba and REEs. Mineral reactions in the system Na-Ca-Fe-Nb-O-H indicate that replacement of pyrochlore by fersmite and columbite occurred at similar conditions with fluid conpositions having relatively low aNa+,moderate aeaH, and mod- erate to high aFeH.Secondary alteration « 150 °C) is charactlerized by the substitutions ANaYF -+ ADYD,ACaYO -+ ADYD,and ACaXO -+ ADXDtogether with moderate to extreme hydration (10-15 wt% H20 or 2-3 molecules per formula unit). -
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 -
Thirteenth List of New Mineral Names. 1 by L. J. SPENCER, M.A., Sc.D., F.R.S
624 Thirteenth list of new mineral names. 1 By L. J. SPENCER, M.A., Sc.D., F.R.S. Keeper of Minerals in the British Museum of Natural History. [Communicated June 7, 1934.] Alkanasul. J. Westman, 1931. Bol. Minero Soc. Nac. Mineria, Santiago de Chile, vol. 43 (a5o 47), p. 433; Zeits. Prakt. Geol., 1932, vol. 40, p. 110. Hydrous basic sulphate of aluminium, potassium, and sodium, K2SO4.Na~SO4.2AI2(SO4)a.6AI(OH)3.6H~O , yellowish-white to bluish-grey, massive, occurring in large amount near Salamanca, Chile. Named from the chemical composition. [Evidently identical with natroalunite.] [M.A. 5-200.] Alleghanyite. C. S. Ross and P. F. Kerr, 1932. Amer. Min., vol. 17, p. 7. Manganese silicate, 5MnO.2Si02, as pink orthorhombic grains, considered to be distinct from tephroite [2MnO.Si02]. Named from the locality, Alleghany County, North Carolina. [M.A. 5-50.] Alumo-chalcosiderite. A. Jahn and E. Gruner, 1933. Mitt. Vogtliind. Gesell. Naturfor., vol. 1, no. 8, p. 19 (Alumo-Chalkosi- derit). A variety of chalcosiderite containing some alumina (Al~O a 10.45 %) replacing ferric oxide. [M.A. 5-391.] Amarillite. H. Ungemach, 1933. Compt. Rend. Acad. Sci. Paris, vol. 197, p. 1133; Bull. Soc. Fran~. Min., [1934], vol. 56 (for 1933), p. 303. Hydrated sulphate of sodium and ferric iron NaFe(SO4)2.6HzO, as yellow monoclinic crystals from Tierra Amarilla, Chile. Named from the locality. [M.A. 5-390.] 1 Previous lists of this series have been given every three years at the ends of vols. 11-22 (1897-1931) of this Magazine. -
Columbium (Niubium) and Tantalum
COLUMBIUM (NIOBIUM) AND TANTALUM By Larry D. Cunningham Domestic survey data and tables were prepared by Robin C. Kaiser, statistical assistant, and the world production table was prepared by Regina R. Coleman, international data coordinator. Columbium [Niobium (Nb)] is vital as an alloying element in economic penalty in most applications. Neither columbium nor steels and in superalloys for aircraft turbine engines and is in tantalum was mined domestically because U.S. resources are of greatest demand in industrialized countries. It is critical to the low grade. Some resources are mineralogically complex, and United States because of its defense-related uses in the most are not currently (2000) recoverable. The last significant aerospace, energy, and transportation industries. Substitutes are mining of columbium and tantalum in the United States was available for some columbium applications, but, in most cases, during the Korean Conflict, when increased military demand they are less desirable. resulted in columbium and tantalum ore shortages. Tantalum (Ta) is a refractory metal that is ductile, easily Pyrochlore was the principal columbium mineral mined fabricated, highly resistant to corrosion by acids, a good worldwide. Brazil and Canada, which were the dominant conductor of heat and electricity, and has a high melting point. pyrochlore producers, accounted for most of total estimated It is critical to the United States because of its defense-related columbium mine production in 2000. The two countries, applications in aircraft, missiles, and radio communications. however, no longer export pyrochlore—only columbium in Substitution for tantalum is made at either a performance or upgraded valued-added forms produced from pyrochlore. -
Geology of the Saint-Marcel Valley Metaophiolites (Northwestern Alps, Italy)
Journal of Maps ISSN: (Print) 1744-5647 (Online) Journal homepage: http://www.tandfonline.com/loi/tjom20 Geology of the Saint-Marcel valley metaophiolites (Northwestern Alps, Italy) Paola Tartarotti, Silvana Martin, Bruno Monopoli, Luca Benciolini, Alessio Schiavo, Riccardo Campana & Irene Vigni To cite this article: Paola Tartarotti, Silvana Martin, Bruno Monopoli, Luca Benciolini, Alessio Schiavo, Riccardo Campana & Irene Vigni (2017) Geology of the Saint-Marcel valley metaophiolites (Northwestern Alps, Italy), Journal of Maps, 13:2, 707-717, DOI: 10.1080/17445647.2017.1355853 To link to this article: http://dx.doi.org/10.1080/17445647.2017.1355853 © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Journal of Maps View supplementary material Published online: 31 Jul 2017. Submit your article to this journal Article views: 24 View related articles View Crossmark data Full Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=tjom20 Download by: [Università degli Studi di Milano] Date: 08 August 2017, At: 01:46 JOURNAL OF MAPS, 2017 VOL. 13, NO. 2, 707–717 https://doi.org/10.1080/17445647.2017.1355853 SCIENCE Geology of the Saint-Marcel valley metaophiolites (Northwestern Alps, Italy) Paola Tartarottia, Silvana Martinb, Bruno Monopolic, Luca Benciolinid, Alessio Schiavoc, Riccardo Campanae and Irene Vignic aDipartimento di Scienze della Terra “Ardito Desio”, Università degli Studi di Milano, Milan, Italy; bDipartimento di -
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. -
Carbonatites of the World, Explored Deposits of Nb and REE—Database and Grade and Tonnage Models
Carbonatites of the World, Explored Deposits of Nb and REE—Database and Grade and Tonnage Models By Vladimir I. Berger, Donald A. Singer, and Greta J. Orris Open-File Report 2009-1139 U.S. Department of the Interior U.S. Geological Survey U.S. Department of the Interior KEN SALAZAR, Secretary U.S. Geological Survey Suzette M. Kimball, Acting Director U.S. Geological Survey, Reston, Virginia: 2009 For product and ordering information: World Wide Web: http://www.usgs.gov/pubprod/ Telephone: 1-888-ASK-USGS For more information on the USGS—the Federal source for science about the Earth, its natural and living resources, natural hazards, and the environment: World Wide Web: http://www.usgs.gov/ Telephone: 1-888-ASK-USGS Suggested citation: Berger, V.I., Singer, D.A., and Orris, G.J., 2009, Carbonatites of the world, explored deposits of Nb and REE— database and grade and tonnage models: U.S. Geological Survey Open-File Report 2009-1139, 17 p. and database [http://pubs.usgs.gov/of/2009/1139/]. Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government. ii Contents Introduction 1 Rules Used 2 Data Fields 2 Preliminary analysis: —Grade and Tonnage Models 13 Acknowledgments 16 References 16 Figures Figure 1. Location of explored Nb– and REE–carbonatite deposits included in the database and grade and tonnage models 4 Figure 2. Cumulative frequency of ore tonnages of Nb– and REE–carbonatite deposits 14 Figure 3 Cumulative frequency of Nb2O5 grades of Nb– and REE–carbonatite deposits 15 Figure 4 Cumulative frequency of RE2O3 grades of Nb– and REE–carbonatite deposits 15 Figure 4 Cumulative frequency of P2O5 grades of Nb– and REE–carbonatite deposits 16 Tables Table 1. -
About Tungsten Mining Emerging Australian Tungsten Developer, Tungsten Mining NL Is an Australian Based Resources Company Listed on the Australian Securities Exchange
Quarterly Report – September 2016 Highlights RC and Diamond drilling confirms shallow potential – During the quarter, the Company drilled 35 RC drillholes for 1,483m and a further 6 diamond drillholes for 234m, targeting shallow mineralisation at Mt Mulgine. Better results included 17 metres at 0.46% WO3 and 0.02% Mo from 2 metres at Mulgine Hill and 72 metres at 0.16% WO3 and 0.02% Mo from surface at Trench. Samples were collected from this program for mineralogical and metallurgical studies, aimed at determining the optimal processing route. Core sampling program delivers encouraging results - Encouraging results achieved from the initial phase of a historical core sampling program at the Mulgine Hill deposit at the Mt Mulgine Project. The reported results, including 8.6m at 0.24% WO3 and 4.9m at 0.18% WO3, highlight the potential to add to existing intersections plus to identify new zones of mineralisation from the historical Minefields and ANZECO drilling. The results of the core sampling program and Q3 drilling program described above will be utilised in development planning and a further update of the geological model and Mineral Resource estimate for Mulgine Hill. Historical diamond hole highlights Trench potential – A review of the Black Dog gold prospect within the Trench deposit has identified significant downhole and strike potential. BDD006 intersected 248m at 0.08% WO3, approximately 100-150m down-dip of the Bobby McGee pit. Mt Mulgine Strategic Development Plan - Tungsten Mining has developed a Strategic Development Plan for the Mt Mulgine Project directed towards the production of tungsten concentrate within 2 years. -
The Metallurgy of Antimony
Chemie der Erde 72 (2012) S4, 3–8 Contents lists available at SciVerse ScienceDirect Chemie der Erde journal homepage: www.elsevier.de/chemer The metallurgy of antimony Corby G. Anderson ∗ Kroll Institute for Extractive Metallurgy, George S. Ansell Department of Metallurgical and Materials Engineering, Colorado School of Mines, Golden, CO 80401, United States article info abstract Article history: Globally, the primary production of antimony is now isolated to a few countries and is dominated by Received 4 October 2011 China. As such it is currently deemed a critical and strategic material for modern society. The metallurgical Accepted 10 April 2012 principles utilized in antimony production are wide ranging. This paper will outline the mineral pro- cessing, pyrometallurgical, hydrometallurgical and electrometallurgical concepts used in the industrial Keywords: primary production of antimony. As well an overview of the occurrence, reserves, end uses, production, Antimony and quality will be provided. Stibnite © 2012 Elsevier GmbH. All rights reserved. Tetrahedrite Pyrometallurgy Hydrometallurgy Electrometallurgy Mineral processing Extractive metallurgy Production 1. Background bullets and armory. The start of mass production of automobiles gave a further boost to antimony, as it is a major constituent of Antimony is a silvery, white, brittle, crystalline solid that lead-acid batteries. The major use for antimony is now as a trioxide exhibits poor conductivity of electricity and heat. It has an atomic for flame-retardants. number of 51, an atomic weight of 122 and a density of 6.697 kg/m3 ◦ ◦ at 26 C. Antimony metal, also known as ‘regulus’, melts at 630 C 2. Occurrence and mineralogy and boils at 1380 ◦C. -