Minerals Named After Scientists
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Tundrite-(Ce) Na3(Ce; La)4(Ti; Nb)2(Sio4)2(CO3)3O4(OH) ² 2H2O C 2001 Mineral Data Publishing, Version 1.2 ° Crystal Data: Triclinic
Tundrite-(Ce) Na3(Ce; La)4(Ti; Nb)2(SiO4)2(CO3)3O4(OH) ² 2H2O c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Triclinic. Point Group: 1: Crystals acicular along [001] and °attened on 010 , to 3 cm; as stellate groups and spherulitic masses. Twinning: On 010 , producing f g f g pseudorhombohedra. Physical Properties: Cleavage: Pronounced on 010 . Fracture: Splintery. f g Tenacity: Brittle. Hardness = 3 D(meas.) = 3.70{4.12 D(calc.) = 4.06 » Optical Properties: Transparent. Color: Brownish yellow, greenish yellow to bright light green. Streak: Yellowish gray. Luster: Vitreous to adamantine. Optical Class: Biaxial (+). Pleochroism: Weak; X = pale yellow; Z = greenish yellow. Orientation: Z c = 4 {14 . ® = 1.743 ¯ = 1.80 ° = 1.88 2V(meas.) = 76 ^ ± ± ± Cell Data: Space Group: P 1: a = 7.533(4) b = 13.924(6) c = 5.010(2) ® = 99±52(2)0 ¯ = 70±50(3)0 ° = 100± 59(2)0 Z = 1 X-ray Powder Pattern: Il¶³maussaq intrusion, Greenland. 13.49 (100), 2.505 (100), 3.448 (90), 2.766 (90), 3.535 (80), 6.784 (70), 1.914 (70) Chemistry: (1) SiO2 10.03 TiO2 12.20 La2O3 8.57 Ce2O3 24.38 Nd2O3 10.25 RE2O3 5.80 Nb2O5 3.44 CaO 0.75 Na2O 8.20 CO3 16.38 Total [100.00] (1) Il¶³maussaq intrusion, Greenland; by electron microprobe, C con¯rmed by loss on ignition; original analysis given as elements, here recalculated to oxides, corresponding to Na3:17(Ce1:78Nd0:73La0:63RE0:41Ca0:16)§=3:71(Ti1:83Nb0:31)§=2:14(SiO4)2:00(CO3)3:27O4:25: Occurrence: In pegmatite veins associated with nepheline syenites. -
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 -
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 -
The Secondary Phosphate Minerals from Conselheiro Pena Pegmatite District (Minas Gerais, Brazil): Substitutions of Triphylite and Montebrasite Scholz, R.; Chaves, M
The secondary phosphate minerals from Conselheiro Pena Pegmatite District (Minas Gerais, Brazil): substitutions of triphylite and montebrasite Scholz, R.; Chaves, M. L. S. C.; Belotti, F. M.; Filho, M. Cândido; Filho, L. Autor(es): A. D. Menezes; Silveira, C. Publicado por: Imprensa da Universidade de Coimbra URL persistente: URI:http://hdl.handle.net/10316.2/31441 DOI: DOI:http://dx.doi.org/10.14195/978-989-26-0534-0_27 Accessed : 2-Oct-2021 20:21:49 A navegação consulta e descarregamento dos títulos inseridos nas Bibliotecas Digitais UC Digitalis, UC Pombalina e UC Impactum, pressupõem a aceitação plena e sem reservas dos Termos e Condições de Uso destas Bibliotecas Digitais, disponíveis em https://digitalis.uc.pt/pt-pt/termos. Conforme exposto nos referidos Termos e Condições de Uso, o descarregamento de títulos de acesso restrito requer uma licença válida de autorização devendo o utilizador aceder ao(s) documento(s) a partir de um endereço de IP da instituição detentora da supramencionada licença. Ao utilizador é apenas permitido o descarregamento para uso pessoal, pelo que o emprego do(s) título(s) descarregado(s) para outro fim, designadamente comercial, carece de autorização do respetivo autor ou editor da obra. Na medida em que todas as obras da UC Digitalis se encontram protegidas pelo Código do Direito de Autor e Direitos Conexos e demais legislação aplicável, toda a cópia, parcial ou total, deste documento, nos casos em que é legalmente admitida, deverá conter ou fazer-se acompanhar por este aviso. pombalina.uc.pt digitalis.uc.pt 9 789892 605111 Série Documentos A presente obra reúne um conjunto de contribuições apresentadas no I Congresso Imprensa da Universidade de Coimbra Internacional de Geociências na CPLP, que decorreu de 14 a 16 de maio de 2012 no Coimbra University Press Auditório da Reitoria da Universidade de Coimbra. -
First Terrestrial Occurrence of Titanium
875 Thz Caradian M fuc ralo g is t Vol.35, pp. 875-885(1997) FIRSTTERRESTRIAL OCCURRENCE OF TITANIUM.RICH PYRRHOTITE, MARCASITEAND PVRITEIN A FENITIZEDXENOLITH FROMTHE KHIBINA ALKALINE COMPLEX. RUSSIA ANDREI Y. BARKOVT nxp KAUKO V.O. LAAJOKI Irxtiruteof Geosciencesand Astrorcmy, University of Oula FIN-90570OuIW FinLand YT]RIP.MEN'SHIKOV Geological Instirute, Kola Science Cente, Russian Acadenry of Scimces, 14 Fersman Street, Apatity 1M200 , Russia TUOMO T. AI.APIETI Instituteof Geoscierrcesand Astrotnnry, University of Ouh+FN-90570 OuIu Finlnnl SEPPOJ. SryONEN Instiarcof ElcctronOptics, University of OuhaFN-90570 Ouh+ Finlnnd ABSTRACT The first terrestrial titanium-rich sulfides, the fust natural niobium-rich sulfide FeMgSe, fluorine-rich (ca. 6 wt.Vo D end-memberphlogopite (S().04 wLTo FeO) and ferroan alabandite occurlocally in aheterogeneous xenolit\ enclosed within nepheline syenite in the l(hifiaa alkalins gs6plex, Kola Peninsul4 northwestem Russia- This assemblage is exclusively associated with an alkali-feldspar-rich rock, probably fenite. Associat€d ninerals include corundum, Nb-Zr-bearing rutile and monazite. The maximum Ti content reaches 3.9 w.7o in pynhotite and 2 wt.7o in marcasite and pyrite, which represent prducts of replacement of the pynhotite. Titanium is distributed rather homogeneously within single grains of the pyrrhotite; however, a strong grain-to-gain variation is observed. The Tl-rich sulfides invariably contrin an elevated level ofvanadium (0.2-0 .4 wr.Vo).T\e results indicate that both Ti and V enter into solid solution in the sulfides. Presumably, there is an environmental similarity between the occurrences ofTl-bearing sulfides in trftibina and in meteorites (enstatite chondrites), where Tl-bearing hoilite occurs. -
: Crystal Structure and Revision of Chemical Formula](https://docslib.b-cdn.net/cover/1463/cafetite-ca-ti2o5-h2o-crystal-structure-and-revision-of-chemical-formula-371463.webp)
Cafetite, Ca[Ti2o5](H2O): Crystal Structure and Revision of Chemical Formula
American Mineralogist, Volume 88, pages 424–429, 2003 Cafetite, Ca[Ti2O5](H2O): Crystal structure and revision of chemical formula SERGEY V. K RIVOVICHEV,1,* VICTOR N. YAKOVENCHUK,2 PETER C. BURNS,3 YAKOV A. PAKHOMOVSKY,2 AND YURY P. MENSHIKOV2 1Department of Crystallography, St. Petersburg State University, University Embankment 7/9, St. Petersburg 199034, Russia 2Geological Institute, Kola Science Centre, Russian Academy of Sciences, Fersmana 14, 184200-RU Apatity, Russia 3Department of Civil Engineering and Geological Sciences, University of Notre Dame, Notre Dame, Indiana 46556-0767, U.S.A. ABSTRACT The crystal structure of cafetite, ideally Ca[Ti2O5](H2O), (monoclinic, P21/n, a = 4.9436(15), b = 12.109(4), c = 15.911(5) Å, b = 98.937(5)∞, V = 940.9(5) Å3, Z = 8) has been solved by direct methods and refined to R1 = 0.057 using X-ray diffraction data collected from a crystal pseudo-merohedrally twinned on (001). There are four symmetrically independent Ti cations; each is octahedrally coordi- nated by six O atoms. The coordination polyhedra around the Ti cations are strongly distorted with individual Ti-O bond lengths ranging from 1.743 to 2.223 Å (the average <Ti-O> bond length is 1.98 Å). Two symmetrically independent Ca cations are coordinated by six and eight anions for Ca1 and Ca2, respectively. The structure is based on [Ti2O5] sheets of TiO6 octahedra parallel to (001). The Ca atoms and H2O groups are located between the sheets and link them into a three-dimensional struc- ture. The structural formula of cafetite confirmed by electron microprobe analysis is Ca[Ti2O5](H2O), . -
38Th RMS Program Notes
E.fu\wsoil 'og PROGRAM Thursday Evening, April 14, 2011 PM 4:00-6:00 Cocktails and Snacks – Hospitality Suite 400 (4th Floor) 6:00-7:45 Dinner – Baxter’s 8:00-9:15 THE GUALTERONI COLLECTION: A TIME CAPSULE FROM A CENTURY AGO – Dr. Renato Pagano In 1950, the honorary curator of the Museum of Natural History in Genoa first introduced Dr. Renato Pagano to mineral collecting as a Boy Scout. He has never looked back. He holds a doctorate in electrical engineering and had a distinguished career as an Italian industrialist. His passion for minerals has produced a collection of more than 13,000 specimens, with both systematic and aesthetic subcollections. His wife Adriana shares his passion for minerals and is his partner in collecting and curating. An excellent profile of Renato, Adriana, and their many collections appeared earlier this year in Mineralogical Record (42:41-52). Tonight Dr. Pagano will talk about an historic mineral collection assembled between 1861 and 1908 and recently acquired intact by the Museum of Natural History of Milan. We most warmly welcome Dr. Renato Pagano back to the speakers’ podium. 9:15 Cocktails and snacks in the Hospitality Suite on the 4th floor will be available throughout the rest of the evening. Dealers’ rooms will be open at this time. All of the dealers are located on the 4th floor. Friday Morning, April 15, 2011 AM 9:00 Announcements 9:15-10:15 CRACKING THE CODE OF PHLOGOPITE DEPOSITS IN QUÉBEC (PARKER MINE), MADAGASCAR (AMPANDANDRAVA) AND RUSSIA (KOVDOR) – Dr. Robert F. Martin Robert François Martin is an emeritus professor of geology at McGill University in Montreal. -
Petrology of Nepheline Syenite Pegmatites in the Oslo Rift, Norway: Zr and Ti Mineral Assemblages in Miaskitic and Agpaitic Pegmatites in the Larvik Plutonic Complex
MINERALOGIA, 44, No 3-4: 61-98, (2013) DOI: 10.2478/mipo-2013-0007 www.Mineralogia.pl MINERALOGICAL SOCIETY OF POLAND POLSKIE TOWARZYSTWO MINERALOGICZNE __________________________________________________________________________________________________________________________ Original paper Petrology of nepheline syenite pegmatites in the Oslo Rift, Norway: Zr and Ti mineral assemblages in miaskitic and agpaitic pegmatites in the Larvik Plutonic Complex Tom ANDERSEN1*, Muriel ERAMBERT1, Alf Olav LARSEN2, Rune S. SELBEKK3 1 Department of Geosciences, University of Oslo, PO Box 1047 Blindern, N-0316 Oslo Norway; e-mail: [email protected] 2 Statoil ASA, Hydroveien 67, N-3908 Porsgrunn, Norway 3 Natural History Museum, University of Oslo, Sars gate 1, N-0562 Oslo, Norway * Corresponding author Received: December, 2010 Received in revised form: May 15, 2012 Accepted: June 1, 2012 Available online: November 5, 2012 Abstract. Agpaitic nepheline syenites have complex, Na-Ca-Zr-Ti minerals as the main hosts for zirconium and titanium, rather than zircon and titanite, which are characteristic for miaskitic rocks. The transition from a miaskitic to an agpaitic crystallization regime in silica-undersaturated magma has traditionally been related to increasing peralkalinity of the magma, but halogen and water contents are also important parameters. The Larvik Plutonic Complex (LPC) in the Permian Oslo Rift, Norway consists of intrusions of hypersolvus monzonite (larvikite), nepheline monzonite (lardalite) and nepheline syenite. Pegmatites ranging in composition from miaskitic syenite with or without nepheline to mildly agpaitic nepheline syenite are the latest products of magmatic differentiation in the complex. The pegmatites can be grouped in (at least) four distinct suites from their magmatic Ti and Zr silicate mineral assemblages. -
Revision 2 of Ms. 5419 Page 1 Time's Arrow in the Trees of Life And
Revision 2 of Ms. 5419 Time’s Arrow in the Trees of Life and Minerals Peter J. Heaney1,* 1Dept. of Geosciences, Penn State University, University Park, PA 16802 *To whom correspondence should be addressed: [email protected] Page 1 Revision 2 of Ms. 5419 1 ABSTRACT 2 Charles Darwin analogized the diversification of species to a Tree of Life. 3 This metaphor aligns precisely with the taxonomic system that Linnaeus developed 4 a century earlier to classify living species, because an underlying mechanism – 5 natural selection – has driven the evolution of new organisms over vast timescales. 6 On the other hand, the efforts of Linnaeus to extend his “universal” organizing 7 system to minerals has been regarded as an epistemological misfire that was 8 properly abandoned by the late nineteenth century. 9 The mineral taxonomies proposed in the wake of Linnaeus can be 10 distinguished by their focus on external character (Werner), crystallography (Haüy), 11 or chemistry (Berzelius). This article appraises the competition among these 12 systems and posits that the chemistry-based Berzelian taxonomy, as embedded 13 within the widely adopted system of James Dwight Dana, ultimately triumphed 14 because it reflects Earth’s episodic but persistent progression with respect to 15 chemical differentiation. In this context, Hazen et al.’s (2008) pioneering work in 16 mineral evolution reveals that even the temporal character of the phylogenetic Tree 17 of Life is rooted within a Danan framework for ordering minerals. 18 19 Page 1 Revision 2 of Ms. 5419 20 INTRODUCTION 21 In an essay dedicated to the evolutionary biologist Ernst Mayr, Stephen Jay 22 Gould (2000) expresses his indignation at the sheer luckiness of Carolus Linnaeus 23 (1707-1778; Fig. -
New Minerals Approved Bythe Ima Commission on New
NEW MINERALS APPROVED BY THE IMA COMMISSION ON NEW MINERALS AND MINERAL NAMES ALLABOGDANITE, (Fe,Ni)l Allabogdanite, a mineral dimorphous with barringerite, was discovered in the Onello iron meteorite (Ni-rich ataxite) found in 1997 in the alluvium of the Bol'shoy Dolguchan River, a tributary of the Onello River, Aldan River basin, South Yakutia (Republic of Sakha- Yakutia), Russia. The mineral occurs as light straw-yellow, with strong metallic luster, lamellar crystals up to 0.0 I x 0.1 x 0.4 rnrn, typically twinned, in plessite. Associated minerals are nickel phosphide, schreibersite, awaruite and graphite (Britvin e.a., 2002b). Name: in honour of Alia Nikolaevna BOG DAN OVA (1947-2004), Russian crys- tallographer, for her contribution to the study of new minerals; Geological Institute of Kola Science Center of Russian Academy of Sciences, Apatity. fMA No.: 2000-038. TS: PU 1/18632. ALLOCHALCOSELITE, Cu+Cu~+PbOZ(Se03)P5 Allochalcoselite was found in the fumarole products of the Second cinder cone, Northern Breakthrought of the Tolbachik Main Fracture Eruption (1975-1976), Tolbachik Volcano, Kamchatka, Russia. It occurs as transparent dark brown pris- matic crystals up to 0.1 mm long. Associated minerals are cotunnite, sofiite, ilin- skite, georgbokiite and burn site (Vergasova e.a., 2005). Name: for the chemical composition: presence of selenium and different oxidation states of copper, from the Greek aA.Ao~(different) and xaAxo~ (copper). fMA No.: 2004-025. TS: no reliable information. ALSAKHAROVITE-Zn, NaSrKZn(Ti,Nb)JSi401ZJz(0,OH)4·7HzO photo 1 Labuntsovite group Alsakharovite-Zn was discovered in the Pegmatite #45, Lepkhe-Nel'm MI. -
Revision #1 the Atomic Arrangement and Electronic Interactions In
This is the peer-reviewed, final accepted version for American Mineralogist, published by the Mineralogical Society of America. The published version is subject to change. Cite as Authors (Year) Title. American Mineralogist, in press. DOI: https://doi.org/10.2138/am-2021-7851. http://www.minsocam.org/ 1 Revision #1 2 3 The atomic arrangement and electronic interactions in vonsenite at 4 295, 100, and 90 K 5 1, 1, 2 3 4 6 MARC MADERAZZO , JOHN M. HUGHES , M. DARBY DYAR , GEORGE R. ROSSMAN , 5 3 6 7 BRANDON J. ACKLEY , ELIZABETH C. SKLUTE , MARIAN V. LUPULESCU , AND 7 8 JEFFREY CHIARENZELLI 9 10 1Department of Geology, University of Vermont, Burlington, Vermont, 05405, U.S.A. 11 2Department of Geology and Environmental Earth Sciences, Miami University, Oxford, Ohio 45056, U.S.A. 12 3Department of Astronomy, Mount Holyoke College, South Hadley, Massachusetts 01075, U.S.A. 13 4Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California 91125- 14 2500, U.S.A. 15 5Department of Chemistry, University of Vermont, Burlington, Vermont, 05405, U.S.A. 16 6New York State Museum, Research and Collections, 3140 CEC, Albany, New York 12230, U.S.A. 17 7Department of Geology, St. Lawrence University, Canton, New York 13617, U.S.A. 18 19 ABSTRACT 2+ 3+ 20 Vonsenite, Fe 2Fe O2BO3, has been the subject of many studies in the materials-science and 21 condensed-matter-physics communities due to interest in the electronic and magnetic properties 22 and ordering behavior of the phase. One such study, undertaken on synthetic material of 23 endmember composition, reports X-ray diffraction structure refinements that indicate a phase 24 transition from Pbam to Pbnm at or just below approximately 283 K, determined subsequently to 25 arise from a Peierls-like instability. -
Brandãoite, [Beal2(PO4)2(OH)2(H2O
Mineralogical Magazine (2019), 83, 261–267 doi:10.1180/mgm.2018.121 Article Brandãoite, [BeAl2(PO4)2(OH)2(H2O)4](H2O), a new Be–Al phosphate mineral from the João Firmino mine, Pomarolli farm region, Divino das Laranjeiras County, Minas Gerais State, Brazil: description and crystal structure † Luiz A. D. Menezes Filho1 , Mário L. S. C. Chaves1, Mark A. Cooper2, Neil A. Ball2, Yassir A. Abdu2,3, Ryan Sharpe2, Maxwell C. Day2 and Frank C. Hawthorne2* 1Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil; 2Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada; and 3Department of Applied Physics and Astronomy, University of Sharjah, P.O. Box 27272, Sharjah, United Arab Emirates Abstract – Brandãoite, [BeAl2(PO4)2(OH)2(H2O)4](H2O), is a new Be Al phosphate mineral from the João Firmino mine, Pomarolli farm region, Divino das Laranjeiras County, Minas Gerais State, Brazil, where it occurs in an albite pocket with other secondary phosphates, including beryllonite, atencioite and zanazziite, in a granitic pegmatite. It occurs as colourless acicular crystals <10 µm wide and <100 µm long that form compact radiating spherical aggregates up to 1.0–1.5 mm across. It is colourless and transparent in single crystals and white in aggregates, has a white streak and a vitreous lustre, is brittle and has conchoidal fracture. Mohs hardness is 6, and the calculated density 3 α β γ is 2.353 g/cm . Brandãoite is biaxial (+), = 1.544, = 1.552 and = 1.568, all ± 0.002; 2Vobs = 69.7(10)° and 2Vcalc = 71.2°.