NEW MINERAL NAMESX Fnq,Nr C. Hnwrnorne, Knnnnth W. Br,Aon
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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 -
MAMMOTHITE: a Pb-Sb-Cu-Al OXY-HYDROXIDE-SULFATE — HYDROGEN ATOM DETERMINATION LOWERS SPACE GROUP SYMMETRY
canmin.52.4.00048 04-03-15 10:50 687 The Canadian Mineralogist Vol. 52, pp. 687-698 (2014) DOI: 10.3749/canmin.1400048 MAMMOTHITE: A Pb-Sb-Cu-Al OXY-HYDROXIDE-SULFATE — HYDROGEN ATOM DETERMINATION LOWERS SPACE GROUP SYMMETRY § JOEL D. GRICE Canadian Museum of Nature, PO Box 3443, Stn D, Ottawa, ON, K1P 6P4, Canada MARK A. COOPER Department of Geological Sciences, University of Manitoba, 125 Dysart Road, Winnipeg, MB, R3T 2N2, Canada ABSTRACT The crystal structure of mammothite, Pb6Cu4AlSbO2(SO4)2Cl4(OH)16, is monoclinic in acentric space group C2, with a 18.959(4), b 7.3398(19), c 11.363(3) Å, β 112.428(9)˚, V 1461.6(1.0) Å3, and Z = 2. It has been refined to an R index of 0.019 on the basis of 3878 observed reflections. There are three crystallographically distinct Pb sites with two different co-ordinations: [Pb1O8Cl1] is a mono-capped square antiprism polyhedron, while [Pb21O7Cl2] and [Pb22O7Cl2] are tri- capped trigonal prisms. Both Cu2+ sites have distorted [4 + 2] octahedral coordination due to the Jahn-Teller effect. The Al and Sb sites are regular-octahedral co-ordination with oxygen atoms. The [SO4] tetrahedron is quite distorted, with S–O bond lengths varying from 1.45 to 1.52 Å and subtended O–S–O angles varying from 106 to 113˚. In the structure there are eight (OH)– anions. All eight H atoms pfu were located, and it is these structure sites that reduce the symmetry from centric to acentric. Although mammothite is classified as a framework structure, it has a distinct layering. -
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. -
THE CRYSTAL STRUCTURE of SHIGAITE, Lalmne*(Oh)Ele(So+Lzna(H2o)6{H2o}6, a HYDROTALCITE.GROUP MINERAL
9L The CanadianMineralo gist Vol. 34, pp. 91,-97(1996) THE CRYSTALSTRUCTURE OF SHIGAITE, lAlMne*(oH)ele(so+lzNa(H2o)6{H2o}6, A HYDROTALCITE.GROUPMINERAL MARK A. COOPERand FRANK C. HAWTHORNE Deparnnewof GeolagicalSciences, University of Manitoba"Winnipeg, Manitoba, R3T 2N2 ABSTRACT The cryslal strucbre of shigaite, tAMnA+(OlD6l3(SOfrNa(H2O)6{HzO}0,rhombohedral, a 9.512(l), c 33.074$) 4,, y 2591.0(8) Ar, Z = 3, R3, hasbeen solved by direct nethods and refined to an R ndex of 4.2Vousing 979 observedreflections measuredwith MoKcl X-radiation.The structuralunit of shigaiteis a planar sheetof edge-sharingoctahedra [AlMna+(OID6]1+. These oxycation sheetsare intercalatedwith oxyanion she€tsof chemical composition Na(H2O)6{H2O}6(SOf2;hydrogen bonding plays a major role in linkage both within the oxyanionsheet and betweenthe structuraluoit and the oxyanionsheet of interstitial species.This work showsshigaite to containessential Na andresults in a significantrevision ofthe chemicalformula- Shigaiteis a hydrotalcite-goup mineral, the Mn2+analogue of motukoreaite. Keywords:shigaite, crystal structure,chemical formul4 hydrogenbonding, hydrotalcite group. Somaanr Nous avons affin6 la stucture de la shigarte, IA1MnS+(OII)613(SO)2Na(H2O)6{HzO}0,rhombo6drique, a 9.512(l), c 33.074(0A, V259L.09)N,z= 3, Rl parm6thoaes directeijusqu'lirnreiiiu n a6l.Z%6nuinsnt979 r6flexionsobserv6es avecun rayonnementMorcr. L'unit6 structuraleest un feuillet d'octabdrese a€tes partag6es,de composition[AlMn3+(OI{)6]11 Ces couchesoxy-cationiques sont intercal6esavec des couchesoxy-anioniques de composition Na(H2O)6{H2O}6(SO)2; les liaisons hydrogdnejouent un role imporanq aussi bien dsns les couchesoxy-anioniques qu'enhe I'unit6 structuraleet la coucheoxy-anionique de I'espbceinterstitielle. -
Design Rules for Discovering 2D Materials from 3D Crystals
Design Rules for Discovering 2D Materials from 3D Crystals by Eleanor Lyons Brightbill Collaborators: Tyler W. Farnsworth, Adam H. Woomer, Patrick C. O'Brien, Kaci L. Kuntz Senior Honors Thesis Chemistry University of North Carolina at Chapel Hill April 7th, 2016 Approved: ___________________________ Dr Scott Warren, Thesis Advisor Dr Wei You, Reader Dr. Todd Austell, Reader Abstract Two-dimensional (2D) materials are championed as potential components for novel technologies due to the extreme change in properties that often accompanies a transition from the bulk to a quantum-confined state. While the incredible properties of existing 2D materials have been investigated for numerous applications, the current library of stable 2D materials is limited to a relatively small number of material systems, and attempts to identify novel 2D materials have found only a small subset of potential 2D material precursors. Here I present a rigorous, yet simple, set of criteria to identify 3D crystals that may be exfoliated into stable 2D sheets and apply these criteria to a database of naturally occurring layered minerals. These design rules harness two fundamental properties of crystals—Mohs hardness and melting point—to enable a rapid and effective approach to identify candidates for exfoliation. It is shown that, in layered systems, Mohs hardness is a predictor of inter-layer (out-of-plane) bond strength while melting point is a measure of intra-layer (in-plane) bond strength. This concept is demonstrated by using liquid exfoliation to produce novel 2D materials from layered minerals that have a Mohs hardness less than 3, with relative success of exfoliation (such as yield and flake size) dependent on melting point. -
New Mineral Names*
American Mineralogist, Volume 71, pages 227-232, 1986 NEW MINERAL NAMES* Pers J. Dulw, Gsoncr Y. CHao, JonN J. FrrzperRrcr, RrcHeno H. LaNcr-nv, MIcHeer- FrerscHnn.aNo JRNBIA. Zncznn Caratiite* sonian Institution. Type material is at the Smithsonian Institu- tion under cataloguenumbers 14981I and 150341.R.H.L. A. M. Clark, E. E. Fejer, and A. G. Couper (1984) Caratiite, a new sulphate-chlorideofcopper and potassium,from the lavas of the 1869 Vesuvius eruption. Mineralogical Magazine, 48, Georgechaoite* 537-539. R. C. Boggsand S. Ghose (1985) GeorgechaoiteNaKZrSi3Or' Caratiite is a sulphate-chloride of potassium and copper with 2HrO, a new mineral speciesfrom Wind Mountain, New Mex- ideal formula K4Cu4Or(SO4).MeCl(where Me : Na and,zorCu); ico. Canadian Mineralogist, 23, I-4. it formed as fine greenacicular crystalsin lava of the 1869 erup- S. Ghose and P. Thakur (1985) The crystal structure of george- tion of Mt. Vesuvius,Naples, Italy. Caratiite is tetragonal,space chaoite NaKZrSi3Or.2HrO. Canadian Mineralogist, 23, 5-10. group14; a : 13.60(2),c : a.98(l) A, Z:2.The strongestlines of the powder partern arc ld A, I, hkll: 9.61(l00Xl l0); Electron microprobe analysis yields SiO, 43.17, 7-xO229.51, 6.80(80X200); 4.296(60X3 I 0); 3.0I 5( 100b)(a 20,32r); 2.747 (7 0) NarO 7.42,IGO I1.28, HrO 8.63,sum 100.010/0,corresponding (4 I t); 2.673(60X5 I 0); 2.478(60)(002); 2. 3 8 8(70Xa 3 l, 50I ); to empirical formula Na, orl(oru(Zro rrTio o,Feo o,)Si, or Oe' 2. -
Joëlbruggerite, Pb3zn3(Sb5+,Te6+)
American Mineralogist, Volume 94, pages 1012–1017, 2009 5+ 6+ 5+ Joëlbruggerite, Pb3Zn3(Sb ,Te )As2O13(OH,O), the Sb analog of dugganite, from the Black Pine mine, Montana STUART J. MILLS ,1,* UWE KOLITSCH ,2 RITSURO MIYAWAKI ,3 LEE A. GROAT ,1 AND GLENN POIRIER 4 1Department of Earth and Ocean Sciences, University of British Columbia, 6339 Stores Road, Vancouver, British Columbia V6T 1Z4, Canada 2Mineralogisch-Petrographische Abteilung, Naturhistorisches Museum Wien, Burgring 7, A-1010 Wien, Austria 3Department of Geology, National Museum of Nature and Science, 3-23-1, Hyakunin-cho, Shinjuku, Tokyo 169-0073, Japan 4Mineral Sciences Division, Canadian Museum of Nature, P.O. Box 3443, Station D, Ottawa, Ontario K1P 6P4, Canada ABSTRACT 5+ 6+ Joëlbruggerite, ideally Pb3Zn3(Sb ,Te )As2O13(OH,O), is a new arsenate mineral (IMA 2008-034) and the Sb5+ analog of dugganite, from the Black Pine mine, 14.5 km northwest of Philipsburg, Granite County, Montana. It is usually found perched on mimetite; other species that may be present include malachite, azurite, pseudomalachite, chalcocite, beudantite-corkite, duftite, dugganite, and kuksite, in milky quartz veins. Joëlbruggerite occurs as barrel-shaped or prismatic crystals up to about 50 µm across in various shades of purple. The crystals have an adamantine luster and a white streak. Mohs hardness is about 3. The fracture is irregular, and the tenacity is brittle. Joëlbruggerite crystals are uniaxial (–), with a calculated refractive index of n = 1.993, and weakly pleochroic: X = Y = gray, Z = purple; absorption: Z > X = Y. Crystals show straight extinction and are length-fast. The empirical chemical formula (mean of 5 electron microprobe analyses) calculated on the basis of 14 [O + OH] 2+ 5+ 6+ anions is Pb3.112(Zn2.689Fe0.185)Σ2.874(Sb0.650Te 0.451)Σ1.101(As1.551P0.203Si0.160)Σ1.914O13.335(OH)0.665. -
JUNE 2021 Contents
................................ 2 NO. 64 64 VOLUME QUARTERLY NEWS BULLETIN ~ JUNE 2 0 2 1 Guest Editorial - Is field geology dead? The Council for Geoscience’s data portal goes live Parahibbingite—a new mineral found in SA .................................................................................................................................................................................................... Volume 64 ~ Number TWO ~ JUNE 2021 contents Society News GSSA MANDELA MINING PRECINCT (FORMERLY CSIR MININGTEK), 2 Guest Editorial - Cameron Penn-Clarke CORNER RUSTENBURG & CARLOW ROADS, 4 Executive Manager’s Corner MELVILLE, SOUTH AFRICA. 6 President’s Column P.O. Box 91230 Auckland Park 2006 8 Media Statement Johannesburg, South Africa 10 The Professional (Affairs) Corner Tel: +27 11 358 0028 e-mail: [email protected] University News Web: www.gssa.org.za 16 Wits School of Geosciences COMMITTEE Convener & Editor: Trishya Owen-Smith ......... 011 559 2677 20 Stellenbosch University Advertising: GSSA Office [email protected] Design & Layout: Belinda Boyes-Varley ........ 079 129 7748 Printing: Seriti Printing (Pty) Ltd ..... 012 843 7632 Articles 22 Parahibbingite—a new mineral found in South Africa All submissions to: Trishya Owen-Smith [email protected] 23 IMA-CNMMN Attach Word .doc + individual high resolution .jpg’s for images 24 The first fossil locality in the Karoo Basin rediscovered 26 AngloGold Ashanti lifts the lid Contributions for the next issue should be submitted by: 15th August, 2021. Mineral Scene Geobulletin is provided free to members of the GSSA. Non- member subscriptions per four issue volume are R350.00 for 30 Shigaite South Africa. Overseas and rest of Africa, R350 plus postage. Surface mail, R200.00. Airmail, R300.00. The views expressed in this magazine are not necessarily those of the GSSA, its editor The Geotraveller or the publishers. -
Shigaite Namn Al3(SO4)
2+ • Shigaite NaMn6 Al3(SO4)2(OH)18 12H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Hexagonal. Point Group: 3. Hexagonal tabular crystals, to 2 cm, may be in groups; as thin films and fracture coatings. Twinning: On {0001}. Physical Properties: Cleavage: On {0001}, perfect. Tenacity: Moderately flexible. Hardness = ∼2 D(meas.) = 2.32 D(calc.) = 2.35 Optical Properties: Semitransparent. Color: Pale yellow, bright yellow, golden yellow, burnt orange; brownish yellow if included, brown to black if altered. Streak: Very pale yellow to white. Luster: Vitreous to dull. Optical Class: Uniaxial (–). Pleochroism: Distinct; O = yellow; E = very pale yellow. Absorption: O > E. ω = 1.546 = n.d. Cell Data: Space Group: R3. a = 9.51–9.52 c = 32.83–33.074 Z = 3 X-ray Powder Pattern: Ioi mine, Japan. 10.89 (100), 5.47 (90), 2.457 (90), 3.664 (80), 2.198 (60), 1.944 (60), 4.36 (40) Chemistry: (1) (2) (3) SO3 13.6 12.75 13.95 Al2O3 15.3 11.8 13.32 Fe2O3 0.9 2.6 MnO 41.7 42.1 37.08 MgO 0.25 Na2O n.d. n.d. 2.70 H2O 28.0 [30.5] 32.95 Total 99.5 [100.0] 100.00 (1) Ioi mine,Japan; by electron microprobe, total Fe as Fe2O3, total Mn as MnO, H2Oby TGA-EGA. (2) Iron Monarch quarry, Australia; by electron microprobe, average of two analyses, • total Fe as Fe2O3, total Mn as MnO, H2O by difference. (3) NaMn6Al3(SO4)2(OH)18 12H2O. Occurrence: A rare secondary mineral in metamorphosed manganese ore deposits. -
Description and Unique Crystal-Structure of Waterhouseite, a New Hydroxy Manganese Phosphate Species from the Iron Monarch Deposit, Middleback Ranges, South Australia
1401 The Canadian Mineralogist Vol. 43, pp. 1401-1410 (2005) DESCRIPTION AND UNIQUE CRYSTAL-STRUCTURE OF WATERHOUSEITE, A NEW HYDROXY MANGANESE PHOSPHATE SPECIES FROM THE IRON MONARCH DEPOSIT, MIDDLEBACK RANGES, SOUTH AUSTRALIA ALLAN PRING§ Department of Mineralogy, South Australian Museum, North Terrace, Adelaide, South Australia 5000, and School of Earth & Environmental Science, University of Adelaide, Adelaide, S.A. 5005, Australia UWE KOLITSCH Institut für Mineralogie und Kristallographie, Geozentrum, Universität Wien, Althanstr. 14, A–1090 Wien, Austria WILLIAM D. BIRCH Department of Mineralogy, Museum of Victoria, GPO Box 666E, Melbourne, Victoria, 3000, Australia ABSTRACT Waterhouseite from the Iron Monarch mine, Iron Knob, South Australia, is a new hydroxy manganese phosphate species that has a unique crystal-structure. The mineral was found in a carbonate-rich zone with gatehouseite, seamanite, rhodochrosite, shigaite, barite, hausmannite and hematite. It occurs as divergent sprays of orange-brown to dark brown bladed crystals up to 1 mm in length but only up to 20 m in thickness. The crystals are transparent with a pearly luster on cleavages, but it is vitreous to pearly on the tabular faces. The mineral is brittle, with a conchoidal fracture and a yellowish brown streak. There is a perfect cleavage on (100) and a probable cleavage on (001). The crystals show the principal forms {100} (dominant), {010}, {011} and {001}. All crystals are twinned on (100) by non-merohedry. The Mohs hardness is estimated to be ~4, and the measured density is 3.55(5) g/cm3 (calculated density is 3.591 g/cm3). Crystals are biaxial negative and length-slow, with ␣ 1.730(3),  ~1.738 and ␥ 1.738(4), but 2V could not be measured. -
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. -
1 Geological Association of Canada Mineralogical
GEOLOGICAL ASSOCIATION OF CANADA MINERALOGICAL ASSOCIATION OF CANADA 2006 JOINT ANNUAL MEETING MONTRÉAL, QUÉBEC FIELD TRIP 4A : GUIDEBOOK MINERALOGY AND GEOLOGY OF THE POUDRETTE QUARRY, MONT SAINT-HILAIRE, QUÉBEC by Charles Normand (1) Peter Tarassoff (2) 1. Département des Sciences de la Terre et de l’Atmosphère, Université du Québec À Montréal, 201, avenue du Président-Kennedy, Montréal, Québec H3C 3P8 2. Redpath Museum, McGill University, 859 Sherbrooke Street West, Montréal, Québec H3A 2K6 1 INTRODUCTION The Poudrette quarry located in the East Hill suite of the Mont Saint-Hilaire alkaline complex is one of the world’s most prolific mineral localities, with a species list exceeding 365. No other locality in Canada, and very few in the world have produced as many species. With a current total of 50 type minerals, the quarry has also produced more new species than any other locality in Canada, and accounts for about 25 per cent of all new species discovered in Canada (Horváth 2003). Why has a single a single quarry with a surface area of only 13.5 hectares produced such a mineral diversity? The answer lies in its geology and its multiplicity of mineral environments. INTRODUCTION La carrière Poudrette, localisée dans la suite East Hill du complexe alcalin du Mont Saint-Hilaire, est l’une des localités minéralogiques les plus prolifiques au monde avec plus de 365 espèces identifiées. Nul autre site au Canada, et très peu ailleurs au monde, n’ont livré autant de minéraux différents. Son total de 50 minéraux type à ce jour place non seulement cette carrière au premier rang des sites canadiens pour la découverte de nouvelles espèces, mais représente environ 25% de toutes les nouvelles espèces découvertes au Canada (Horváth 2003).