New Mineral Names*
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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 -
General Index
CAL – CAL GENERAL INDEX CACOXENITE United States Prospect quarry (rhombs to 3 cm) 25:189– Not verified from pegmatites; most id as strunzite Arizona 190p 4:119, 4:121 Campbell shaft, Bisbee 24:428n Unanderra quarry 19:393c Australia California Willy Wally Gully (spherulitic) 19:401 Queensland Golden Rule mine, Tuolumne County 18:63 Queensland Mt. Isa mine 19:479 Stanislaus mine, Calaveras County 13:396h Mt. Isa mine (some scepter) 19:479 South Australia Colorado South Australia Moonta mines 19:(412) Cresson mine, Teller County (1 cm crystals; Beltana mine: smithsonite after 22:454p; Brazil some poss. melonite after) 16:234–236d,c white rhombs to 1 cm 22:452 Minas Gerais Cripple Creek, Teller County 13:395–396p,d, Wallaroo mines 19:413 Conselheiro Pena (id as acicular beraunite) 13:399 Tasmania 24:385n San Juan Mountains 10:358n Renison mine 19:384 Ireland Oregon Victoria Ft. Lismeenagh, Shenagolden, County Limer- Last Chance mine, Baker County 13:398n Flinders area 19:456 ick 20:396 Wisconsin Hunter River valley, north of Sydney (“glen- Spain Rib Mountain, Marathon County (5 mm laths donite,” poss. after ikaite) 19:368p,h Horcajo mines, Ciudad Real (rosettes; crystals in quartz) 12:95 Jindevick quarry, Warregul (oriented on cal- to 1 cm) 25:22p, 25:25 CALCIO-ANCYLITE-(Ce), -(Nd) cite) 19:199, 19:200p Kennon Head, Phillip Island 19:456 Sweden Canada Phelans Bluff, Phillip Island 19:456 Leveäniemi iron mine, Norrbotten 20:345p, Québec 20:346, 22:(48) Phillip Island 19:456 Mt. St-Hilaire (calcio-ancylite-(Ce)) 21:295– Austria United States -
The Veladero High-Sulfidation Epithermal Au-Ag Deposit
THE VELADERO HIGH-SULFIDATION EPITHERMAL AU-AG DEPOSIT, ARGENTINA: VOLCANIC STRATIGRAPHY, ALTERATION, MINERALIZATION, AND QUARTZ PARAGENESIS by Elizabeth A. Holley A thesis submitted to the Faculty and the Board of Trustees of the Colorado School of Mines in partial fulfillment of the requirements for the degree of Doctor of Philosophy (Geology). Golden, Colorado Date _________________ Signed:___________________________ Elizabeth A. Holley Signed:___________________________ Dr. Thomas Monecke Thesis Advisor Golden, Colorado Date _________________ Signed:___________________________ Dr. J. D. Humphrey Associate Professor and Head Department of Geology and Geological Engineering ii ABSTRACT The Veladero Au-Ag high-sulfidation epithermal deposit is located in the El Indio-Pasuca belt in Argentina. Veladero is an oxidized deposit that contained reserves of 12.2 Moz of Au and 226.2 Moz of Ag at the end of 2008. Ore is primarily hosted in silicified breccias. The volcanic package at Veladero is a coalescing complex of domes, diatremes, and hydrothermal breccia bodies, mantled by a thick apron of volcaniclastic deposits. These units are inferred to be of Cerro de las Tórtolas age (16.0 ± 0.2 to 14.9 ± 0.7 Ma) at Amable in the southern part of the Veladero area, and Vacas Heladas age (12.7 ± 0.9 to 11.0 ± 0.2 Ma) at Filo Federico in the northern part of Veladero. Emplacement of hydrothermal breccia units was accompanied or shortly followed by multiple pulses of magmatic-hydrothermal and alternating jarosite alteration from about 15.4 to 8.9 Ma. Alunite and jarosite 40Ar-39Ar ages and U-Pb zircon ages of crosscutting dikes restrict mineralization at Amable to the period from 15.4 to 12.14 0.11 Ma, probably commencing closer to 12.7 Ma. -
Thirty-Seventh List of New Mineral Names. Part 1" A-L
Thirty-seventh list of new mineral names. Part 1" A-L A. M. CLARK Department of Mineralogy, The Natural History Museum, Cromwell Road, London SW7 5BD, UK AND V. D. C. DALTRYt Department of Geology and Mineralogy, University of Natal, Private Bag XO1, Scottsville, Pietermaritzburg 3209, South Africa THE present list is divided into two sections; the pegmatites at Mount Alluaiv, Lovozero section M-Z will follow in the next issue. Those Complex, Kola Peninsula, Russia. names representing valid species, accredited by the Na19(Ca,Mn)6(Ti,Nb)3Si26074C1.H20. Trigonal, IMA Commission on New Minerals and Mineral space group R3m, a 14.046, c 60.60 A, Z = 6. Names, are shown in bold type. Dmeas' 2.76, Dc~ac. 2.78 g/cm3, co 1.618, ~ 1.626. Named for the locality. Abenakiite-(Ce). A.M. McDonald, G.Y. Chat and Altisite. A.P. Khomyakov, G.N. Nechelyustov, G. J.D. Grice. 1994. Can. Min. 32, 843. Poudrette Ferraris and G. Ivalgi, 1994. Zap. Vses. Min. Quarry, Mont Saint-Hilaire, Quebec, Canada. Obschch., 123, 82 [Russian]. Frpm peralkaline Na26REE(SiO3)6(P04)6(C03)6(S02)O. Trigonal, pegmatites at Oleny Stream, SE Khibina alkaline a 16.018, c 19.761 A, Z = 3. Named after the massif, Kola Peninsula, Russia. Monoclinic, a Abenaki Indian tribe. 10.37, b 16.32, c 9.16 ,~, l~ 105.6 ~ Z= 2. Named Abswurmbachite. T. Reinecke, E. Tillmanns and for the chemical elements A1, Ti and Si. H.-J. Bernhardt, 1991. Neues Jahrb. Min. Abh., Ankangite. M. Xiong, Z.-S. -
New Mineral Names*,†
American Mineralogist, Volume 106, pages 1537–1543, 2021 New Mineral Names*,† Dmitriy I. Belakovskiy1 and Yulia Uvarova2 1Fersman Mineralogical Museum, Russian Academy of Sciences, Leninskiy Prospekt 18 korp. 2, Moscow 119071, Russia 2CSIRO Mineral Resources, ARRC, 26 Dick Perry Avenue, Kensington, Western Australia 6151, Australia In this issue This New Mineral Names has entries for 11 new species, including bohuslavite, fanfaniite, ferrierite-NH4, feynmanite, hjalmarite, kenngottite, potassic-richterite, rockbridgeite-group minerals (ferrirockbridgeite and ferro- rockbridgeite), rudabányaite, and strontioperloffite. Bohuslavite* show a very strong and broad absorption in the O–H stretching region –1 D. Mauro, C. Biagoni, E. Bonaccorsi, U. Hålenius, M. Pasero, H. Skogby, (3600–3000 cm ) and a prominent band at 1630 (H–O–H bending) with F. Zaccarini, J. Sejkora, J. Plášil, A.R. Kampf, J. Filip, P. Novotný, a shoulder indicating two slightly different H2O environments in the –1 3+ structure. The weaker band at ~5100 cm is assigned to H2O combination R. Škoda, and T. Witzke (2019) Bohuslavite, Fe4 (PO4)3(SO4)(OH) mode (bending + stretching). The IR spectrum of bohuslavite from HM (H2O)10·nH2O, a new hydrated iron phosphate-sulfate. European Journal of Mineralogy, 31(5-6), 1033–1046. shows bands at: 3350, 3103, 1626, 1100, 977, 828, 750, 570, and 472 cm–1. Polarized optical absorption spectra show absorption bands due to 3+ 3+ electronic transitions in octahedrally coordinated Fe at 23 475, 22 000, Bohuslavite (2018-074a), ideally Fe4 (PO4)3(SO4)(OH)(H2O)10·nH2O, –1 triclinic, was discovered in two occurrences, in the Buca della Vena baryte and 18 250 cm . -
New Mineral Names*
---- -- American Mineralogist, Volume 70, pages 214-221, 1985 NEW MINERAL NAMES* PETE J. DUNN, GEORGE Y. CHAO, MICHAEL FLEISCHER, JAMES A. FERRAIOLO, RICHARD H. LANGLEY, ADOLF PAaST, AND JANET A. ZILCZER Bulachlte* (RE1.7tFeij:1i5 Tho.03Po.01h:=I.80 C5.15015.95 F 1.94,(Ba2.47SrO.02Cao.06 K. Walenta (1983) Bulachite, a new aluminum arsenate mineral Nao.3s~.07h:-3.00 (RE1.63Feij~ Tho.02AIo.01h:-1.70C5.23015.ssF2.56 and (Ba2.53SrO.03CaO.t3Nao.24Ko.07h:-3.00 (REt.66 Tho.02Po.os from Neubulach in the northern Black Forest. Der Aufschluss, 34,445-451 (in German). Alo.01h:- J.70C4.96015.66F1.SS,or ideally Ba3Ce2(C03hF2' The min- erai dissolves readily in dilute HCI and in other strong inorganic Chemical analysis gave Ah03 37.2, AS205 39.1 and H20 (by acids. weight loss) 25.5, sum 101.8%, leading to the idealized formula Weissenberg photographs, four-circle single-crystal diffrac- Ah(As04)(OHh . 3H20. Bulachite is easily soluble in HCII: I, tometry and electron diffraction show the mineral to be mono- less easily in HN03 I: I. clinic, C2/m, Cm or C2, a = 21.4256, b = 5.0348, c = 13.2395A, Dimensions of the orthorhombic unit cell, as determined from (3= 94.613°. There is a pronounced rhombohedral subcell with a' an indexed X-ray powder diffraction pattern, are: a 15.53, b = 5.11, c' = 9.8A, similar to the subcell of huanghoite (Am. 17.78, c 7.03A, Z = 10, D (meas.) 2.60, (calc.) 2.55. The Mineral., 48, 1179, 1963). -
Shin-Skinner January 2018 Edition
Page 1 The Shin-Skinner News Vol 57, No 1; January 2018 Che-Hanna Rock & Mineral Club, Inc. P.O. Box 142, Sayre PA 18840-0142 PURPOSE: The club was organized in 1962 in Sayre, PA OFFICERS to assemble for the purpose of studying and collecting rock, President: Bob McGuire [email protected] mineral, fossil, and shell specimens, and to develop skills in Vice-Pres: Ted Rieth [email protected] the lapidary arts. We are members of the Eastern Acting Secretary: JoAnn McGuire [email protected] Federation of Mineralogical & Lapidary Societies (EFMLS) Treasurer & member chair: Trish Benish and the American Federation of Mineralogical Societies [email protected] (AFMS). Immed. Past Pres. Inga Wells [email protected] DUES are payable to the treasurer BY January 1st of each year. After that date membership will be terminated. Make BOARD meetings are held at 6PM on odd-numbered checks payable to Che-Hanna Rock & Mineral Club, Inc. as months unless special meetings are called by the follows: $12.00 for Family; $8.00 for Subscribing Patron; president. $8.00 for Individual and Junior members (under age 17) not BOARD MEMBERS: covered by a family membership. Bruce Benish, Jeff Benish, Mary Walter MEETINGS are held at the Sayre High School (on Lockhart APPOINTED Street) at 7:00 PM in the cafeteria, the 2nd Wednesday Programs: Ted Rieth [email protected] each month, except JUNE, JULY, AUGUST, and Publicity: Hazel Remaley 570-888-7544 DECEMBER. Those meetings and events (and any [email protected] changes) will be announced in this newsletter, with location Editor: David Dick and schedule, as well as on our website [email protected] chehannarocks.com. -
New Mineral Names*
American Mineralogist, Volume 83, pages 400±403, 1998 NEW MINERAL NAMES* JOHN L. JAMBOR1 AND ANDREW C. ROBERTS2 1Department of Earth Sciences, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada 2Geological Survey of Canada, 601 Booth Street, Ottawa, Ontario K1A 0G1, Canada Benyacarite* from the results of a crystal structure determination. The F. Demartin, T. Pilati, H.D. Gay, C.M. Gramaccioli (1993) empirical formula on the basis of 23 anions is The crystal structure of a mineral related to paulkerrite. (Ca3.00K0.01)S3.01B5O6(OH)7Cl1.99´8H2O. The mineral occurs Zeits. Kristallogr., 208, 57±71. as micaceous grains, 0.5 3 0.25 3 0.1 mm, that form F. Demartin, H.D. Gay, C.M. Gramaccioli, T. Pilati (1997) cleavable masses up to 2 3 1 3 1 mm. Colorless to white, Benyacarite, a new titanium-bearing phosphate mineral transparent to translucent, vitreous luster, white streak, species from Cerro Blanco, Argentina. Can. Mineral., ¯exible, micaceous, perfect {010} cleavage, H 5 5, 35, 707±712. twinned on (010), non¯uorescent, Dmeas 5 1.97(3), Dcalc 5 Chemical data in the 1993 paper were abstracted in 1.93 g/cm3 for Z 5 2. The IR spectrum shows the pres- Am. Mineral., 79, p. 763, 1994. On the basis of Z 5 4, ence of H2O groups and complex borate groups. Optically 21 the empirical formula is [(H2O)0.78K0.16Na0.03]2 Ti(Mn V0.75 biaxial negative, a51.506(2), b51.527(2), g5 21 31 41 Fe0.21 Mg0.04)2(Fe 0.68 Ti 0.28 Al0.07)2(PO4)4(O0.6F0.4)2´14H2O, The 1.532(2), 2Vmeas 5 56(1), 2Vcalc 5 51.48, orientation Z 5 mineral occurs as euhedral tabular to almost equidimen- b, X ` c 5 308 in the obtuse angle b. -
Capgaronnite, Hgs'ag(Clrbrri), a New Sulfide-Halide Mineral from Var, France
American Mineralogist, Volume 77, pages 197-200, 1992 Capgaronnite, HgS'Ag(ClrBrrI), a new sulfide-halide mineral from Var, France Bnr.lN MlsoN National Museum of Natural History, Smithsonian Institution, Washington, DC 20560, U.S.A. Wrr-r.r,LnnG. Murvrpm CSIRO Division of Mineral Products, P.O. Box l24,Port Melbourne, Victoria 3207, Australia Hl.r,rr- S.q,RP Department of Mineralogy, Natural History Museum, P.O. Box 434, Geneva, Switzerland AssrRAcr Capgaronnite,ideally HgAg(Cl,Br,I)S, is a new mineral from the Cap-Garonnecopper- lead mine, Var, France. The mineral is orthorhombic, space gtoup P2t2r2' with a : 6.803(8), b : 12.87(l), c -- 4.528(7), and Z :4. The composition and crystal structure of capgaronnite are related to those of perroudite [5HgS.4Ag(Cl,Br,I)] previously reported from the Cap-Garonne locality. Like perroudite, capga.ronnite probably crystallized fol- lowing decomposition of Hg- and Ag-bearing tennantite by halide-bearing solutions of marine origin. Capgaronnite is pleochroic in very thin splinters, with a : dark brown and 7 : gray to clear purple. The optical orientation is a : c, P : b, and "t : a' Indices of refraction measured by reflectance measurements on oriented crystals in polished section were d - : 2.2, t - 2.3; 0 could not be measuredbecause the crystalsare very thin parallel to B 6. A preliminary solution of the capgaronniteatomic iurangement(R : 0.17) was obtained from X-ray film intensities.In capgaronnite,(010) layers of face-sharedHg octahedrabuilt around chains ofcontinuous -S-Hg-S- bonds arejoined by cross-linked,paired groups of Ag tetrahedra. -
Capgaronnite, Hgs. Ag(CI,Br ,1), a New Sulfide-Halide ]Ti1ineralfrom
American Mineralogist, Volume 77, pages 197-200, 1992 Capgaronnite, HgS. Ag( CI,Br ,1), a new sulfide-halide ]tI1ineralfrom Var, France BRIAN MASON National Museum of Natural History, Smithsonian Institution, Washington, DC 20560, U.S.A. WILLIAM G. MUMME CSIRO Division of Mineral Products, P.o. Box 124, Port Melbounle, Victoria 3207, Australia HALIL SARP Department of Mineralogy, Natural History Museum, P.O. Box 434, Geneva, Switzerland ABSTRACT Capgaronnite, ideally HgAg(Cl,Br,I)S, is a new mineral from. the Cap-Garonne copper- lead mine, Var, France. The mineral is orthorhombic, spac~~ group P2t2t2, with a = 6.803(8), b = 12.87(1), c = 4.528(7), and Z = 4. The composition and crystal structure of capgaronnite are related to those of perroudite [5HgS. 4Ag(Cl,Br,I)] previously reported from the Cap-Garonne locality. Like perroudite, capgaronnite probably crystallized fol- lowing decomposition of Hg- and Ag-bearing tennantite by halide-bearing solutions of marine origin. Capgaronnite is pleochroic in very thin splinters, with a = dark brown and 'Y= gray to clear purple. The optical orientation is a = c, {3= b, and 'Y = a. Indices of refraction measured by reflectance measurements on oriented crystals in polished section were a f'"'W 2.2, 'Yf'"'W2.3; {3could not be measured because the crystals are very thin parallel to {3= b. A preliminary solution of the capgaronnite atomic arrangement (R = 0.17) was obtained from X-ray film intensities. In capgaronnite, (010) layers offace-shared Hg octahedra built around chains of continuous -S-Hg-S- bonds are joined by cross-linked, paired groups of Ag tetrahedra. -
Hgsag(Cl, Br) : Un Nouveau Minéral De La Mine De Cap Garonne, Var (France) : Polymorphe De La Capgaronnite
L'iltisite : HgSAg(Cl, Br) : un nouveau minéral de la mine de Cap Garonne, Var (France) : polymorphe de la capgaronnite Autor(en): Sarp, Halil / Sanz-Gysler, Jan / Perroud, Pierre Objekttyp: Article Zeitschrift: Archives des sciences et compte rendu des séances de la Société Band (Jahr): 50 (1997) Heft 1: Archives des Sciences PDF erstellt am: 30.09.2021 Persistenter Link: http://doi.org/10.5169/seals-740261 Nutzungsbedingungen Die ETH-Bibliothek ist Anbieterin der digitalisierten Zeitschriften. Sie besitzt keine Urheberrechte an den Inhalten der Zeitschriften. Die Rechte liegen in der Regel bei den Herausgebern. Die auf der Plattform e-periodica veröffentlichten Dokumente stehen für nicht-kommerzielle Zwecke in Lehre und Forschung sowie für die private Nutzung frei zur Verfügung. Einzelne Dateien oder Ausdrucke aus diesem Angebot können zusammen mit diesen Nutzungsbedingungen und den korrekten Herkunftsbezeichnungen weitergegeben werden. Das Veröffentlichen von Bildern in Print- und Online-Publikationen ist nur mit vorheriger Genehmigung der Rechteinhaber erlaubt. Die systematische Speicherung von Teilen des elektronischen Angebots auf anderen Servern bedarf ebenfalls des schriftlichen Einverständnisses der Rechteinhaber. Haftungsausschluss Alle Angaben erfolgen ohne Gewähr für Vollständigkeit oder Richtigkeit. Es wird keine Haftung übernommen für Schäden durch die Verwendung von Informationen aus diesem Online-Angebot oder durch das Fehlen von Informationen. Dies gilt auch für Inhalte Dritter, die über dieses Angebot zugänglich sind. Ein Dienst der ETH-Bibliothek ETH Zürich, Rämistrasse 101, 8092 Zürich, Schweiz, www.library.ethz.ch http://www.e-periodica.ch Archs Sei. Genève Vol. 50 Fase. I pp. 1 -5 Avril 1997 L'ILTISITE, HgSAg(Cl.Br), UN NOUVEAU MINÉRAL DE LA MINE DE CAP GARONNE, VAR (FRANCE), POLYMORPHE DE LA CAPGARONNITE PAR Halil SARP*, Jan SANZ-GYSLER* & Pierre PERROUD* (Afx rep» /e 7 S. -
IMA–CNMNC Approved Mineral Symbols
Mineralogical Magazine (2021), 85, 291–320 doi:10.1180/mgm.2021.43 Article IMA–CNMNC approved mineral symbols Laurence N. Warr* Institute of Geography and Geology, University of Greifswald, 17487 Greifswald, Germany Abstract Several text symbol lists for common rock-forming minerals have been published over the last 40 years, but no internationally agreed standard has yet been established. This contribution presents the first International Mineralogical Association (IMA) Commission on New Minerals, Nomenclature and Classification (CNMNC) approved collection of 5744 mineral name abbreviations by combining four methods of nomenclature based on the Kretz symbol approach. The collection incorporates 991 previously defined abbreviations for mineral groups and species and presents a further 4753 new symbols that cover all currently listed IMA minerals. Adopting IMA– CNMNC approved symbols is considered a necessary step in standardising abbreviations by employing a system compatible with that used for symbolising the chemical elements. Keywords: nomenclature, mineral names, symbols, abbreviations, groups, species, elements, IMA, CNMNC (Received 28 November 2020; accepted 14 May 2021; Accepted Manuscript published online: 18 May 2021; Associate Editor: Anthony R Kampf) Introduction used collection proposed by Whitney and Evans (2010). Despite the availability of recommended abbreviations for the commonly Using text symbols for abbreviating the scientific names of the studied mineral species, to date < 18% of mineral names recog- chemical elements