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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 -
Alamosite Pbsio3 C 2001 Mineral Data Publishing, Version 1.2 ° Crystal Data: Monoclinic
Alamosite PbSiO3 c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Monoclinic. Point Group: 2=m: Crystals ¯brous [010]; as radiating aggregates and balls, to 7.5 cm. k Physical Properties: Cleavage: Perfect on 010 . Hardness = 4.5 D(meas.) = 6.488(3) D(calc.) = [6.30] f g Optical Properties: Transparent to translucent. Color: Colorless to white, cream, or light gray. Luster: Adamantine. Optical Class: Biaxial ({). Orientation: Y = b. Dispersion: r < v; strong, weak inclined. ® = 1.945{1.947 ¯ = 1.955{1.961 ° = 1.959{1.968 2V(meas.) = 65± Cell Data: Space Group: P 2=n: a = 12.247 b = 7.059 c = 11.236 ¯ = 113:12± Z = 12 X-ray Powder Pattern: Tsumeb, Namibia. 3.34 (100), 3.56 (95), 3.53 (75), 2.300 (75), 3.23 (70), 2.987 (70), 3.25 (60) Chemistry: (1) (2) (3) SiO2 21.11 20.01 21.21 Al2O3 0.09 FeO 0.09 0.18 MnO 0.02 PbO 78.13 78.95 78.79 CaO trace 0.09 insol: 0.61 Total 99.94 99.34 100.00 (1) Alamos, Mexico. (2) Tsumeb, Namibia; by electron microprobe. (3) PbSiO3: Occurrence: As a rare secondary mineral in the oxidized zone of lead-bearing base metal deposits. Association: Wulfenite, leadhillite, cerussite (Alamos, Mexico); leadhillite, anglesite, melanotekite, °eischerite, kegelite, hematite (Tsumeb, Namibia); diaboleite, phosgenite, cerussite, wulfenite, willemite (Tiger, Arizona, USA); melanotekite, shattuckite, wickenburgite (Rawhide mine, Arizona, USA). Distribution: From Mexico, in Sonora, at Alamos, and the San Pascual mine, near Zimap¶an, Hidalgo. In the USA, from Arizona, in the Mammoth-St. -
Infrare D Transmission Spectra of Carbonate Minerals
Infrare d Transmission Spectra of Carbonate Mineral s THE NATURAL HISTORY MUSEUM Infrare d Transmission Spectra of Carbonate Mineral s G. C. Jones Department of Mineralogy The Natural History Museum London, UK and B. Jackson Department of Geology Royal Museum of Scotland Edinburgh, UK A collaborative project of The Natural History Museum and National Museums of Scotland E3 SPRINGER-SCIENCE+BUSINESS MEDIA, B.V. Firs t editio n 1 993 © 1993 Springer Science+Business Media Dordrecht Originally published by Chapman & Hall in 1993 Softcover reprint of the hardcover 1st edition 1993 Typese t at the Natura l Histor y Museu m ISBN 978-94-010-4940-5 ISBN 978-94-011-2120-0 (eBook) DOI 10.1007/978-94-011-2120-0 Apar t fro m any fair dealin g for the purpose s of researc h or privat e study , or criticis m or review , as permitte d unde r the UK Copyrigh t Design s and Patent s Act , 1988, thi s publicatio n may not be reproduced , stored , or transmitted , in any for m or by any means , withou t the prio r permissio n in writin g of the publishers , or in the case of reprographi c reproductio n onl y in accordanc e wit h the term s of the licence s issue d by the Copyrigh t Licensin g Agenc y in the UK, or in accordanc e wit h the term s of licence s issue d by the appropriat e Reproductio n Right s Organizatio n outsid e the UK. Enquirie s concernin g reproductio n outsid e the term s state d here shoul d be sent to the publisher s at the Londo n addres s printe d on thi s page. -
Mottramite Pbcu(VO4)(OH) C 2001-2005 Mineral Data Publishing, Version 1 Crystal Data: Orthorhombic
Mottramite PbCu(VO4)(OH) c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Orthorhombic. Point Group: 2/m 2/m 2/m. As crystals, equant or dipyramidal {111}, prismatic [001] or [100], with {101}, {201}, many others, to 3 mm, in drusy crusts, botryoidal, usually granular to compact, massive. Physical Properties: Fracture: Small conchoidal to uneven. Tenacity: Brittle. Hardness = 3–3.5 D(meas.) = ∼5.9 D(calc.) = 6.187 Optical Properties: Transparent to nearly opaque. Color: Grass-green, olive-green, yellow- green, siskin-green, blackish brown, nearly black. Streak: Yellowish green. Luster: Greasy. Optical Class: Biaxial (–), rarely biaxial (+). Pleochroism: Weak to strong; X = Y = canary-yellow to greenish yellow; Z = brownish yellow. Orientation: X = c; Y = b; Z = a. Dispersion: r> v,strong; rarely r< v.α= 2.17(2) β = 2.26(2) γ = 2.32(2) 2V(meas.) = ∼73◦ Cell Data: Space Group: P nma. a = 7.667–7.730 b = 6.034–6.067 c = 9.278–9.332 Z=4 X-ray Powder Pattern: Mottram St. Andrew, England; close to descloizite. 3.24 (vvs), 5.07 (vs), 2.87 (vs), 2.68 (vs), 2.66 (vs), 2.59 (vs), 1.648 (vs) Chemistry: (1) (2) (1) (2) CrO3 0.50 ZnO 0.31 10.08 P2O5 0.24 PbO 55.64 55.30 As2O5 1.33 H2O 3.57 2.23 V2O5 21.21 22.53 insol. 0.17 CuO 17.05 9.86 Total 100.02 100.00 (1) Bisbee, Arizona, USA; average of three analyses. (2) Pb(Cu, Zn)(VO4)(OH) with Zn:Cu = 1:1. -
Crimsonite, Pbfe23+(PO4)
Mineralogical Magazine, October 2016, Vol. 80(6), pp. 925–935 3+ Crimsonite, PbFe2 (PO4)2(OH)2, the phosphate analogue of carminite from the Silver Coin mine, Valmy, Nevada, USA 1,* 2 3 4 A. R. KAMPF ,P.M.ADAMS ,S.J.MILLS AND B. P. NASH 1 Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, CA 90007, USA 2 126 South Helberta Avenue #2, Redondo Beach, California 90277, USA 3 Geosciences, Museum Victoria, GPO Box 666, Melbourne 3001, Victoria, Australia 4 Department of Geology and Geophysics, University of Utah, Salt Lake City, UT 84112, USA [Received 28 May 2015; Accepted 10 September 2015; Associate Editor: Ian Graham] ABSTRACT 3þ Crimsonite (IMA2014-095), PbFe2 (PO4)2(OH)2, the phosphate analogue of carminite, is a new mineral from the Silver Coin mine, Valmy, Iron Point district, Humboldt County, Nevada, USA, where it occurs as a low-temperature secondary mineral in association with fluorwavellite, goethite, hematite, hentschelite, plumbogummite and variscite on quartz. Crimsonite occurs in subparallel aggregates of deep red blades or plates flattened on {100} and up to 0.1 mm in maximum dimension. The streak is light purplish orange. Crystals are transparent and have adamantine lustre. The Mohs hardness is ∼3½, the tenacity is brittle, the fracture is irregular to splintery and an imperfect cleavage is likely on {101}. The calculated density is 5.180 g/cm3. Crimsonite is optically biaxial (+), with 2V = 85.5(5)° and γ – α = 0.011. Using the Gladstone- Dale relationship, the calculated indices of refraction are α = 2.021, β = 2.026 and γ = 2.032. -
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. -
Topographical Index
997 TOPOGRAPHICAL INDEX EUROPE Penberthy Croft, St. Hilary: carminite, beudantite, 431 Iceland (fsland) Pengenna (Trewethen) mine, St. Kew: Bondolfur, East Iceland: pitchsbone, beudantite, carminite, mimetite, sco- oligoclase, 587 rodite, 432 Sellatur, East Iceland: pitchs~one, anor- Redruth: danalite, 921 thoclase, 587 Roscommon Cliff, St. Just-in-Peuwith: Skruthur, East Iceland: pitchstonc, stokesite, 433 anorthoclase, 587 St. Day: cornubite, 1 Thingmuli, East Iceland: andesine, 587 Treburland mine, Altarnun: genthelvite, molybdenite, 921 Faroes (F~eroerne) Treore mine, St. Teath: beudantite, carminite, jamesonite, mimetite, sco- Erionite, chabazite, 343 rodite, stibnite, 431 Tretoil mine, Lanivet: danalite, garnet, Norway (Norge) ilvaite, 921 Gryting, Risor: fergusonite (var. risSrite), Wheal Betsy, Tremore, Lanivet: he]vine, 392 scheelite, 921 Helle, Arendal: fergusonite, 392 Wheal Carpenter, Gwinear: beudantite, Nedends: fergusonite, 392 bayldonite, carminite, 431 ; cornubite, Rullandsdalen, Risor: fergusonite, 392 cornwallite, 1 Wheal Clinton, Mylor, Falmouth: danal- British Isles ire, 921 Wheal Cock, St. Just-in- Penwith : apatite, E~GLA~D i~D WALES bertrandite, herderite, helvine, phena- Adamite, hiibnerite, xliv kite, scheelite, 921 Billingham anhydrite mine, Durham: Wheal Ding (part of Bodmin Wheal aph~hitalite(?), arsenopyrite(?), ep- Mary): blende, he]vine, scheelite, 921 somite, ferric sulphate(?), gypsum, Wheal Gorland, Gwennap: cornubite, l; halite, ilsemannite(?), lepidocrocite, beudantite, carminite, zeunerite, 430 molybdenite(?), -
Descloizite Pbzn(VO4)(OH) C 2001-2005 Mineral Data Publishing, Version 1
Descloizite PbZn(VO4)(OH) c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Orthorhombic. Point Group: 2/m 2/m 2/m. As crystals, equant or pyramidal {111}, prismatic [001] or [100], or tabular {100}, with {101}, {201}, many others, rarely skeletal, to 5 cm, commonly in drusy crusts, stalactitic or botryoidal, coarsely fibrous, granular to compact, massive. Physical Properties: Fracture: Small conchoidal to uneven. Tenacity: Brittle. Hardness = 3–3.5 D(meas.) = ∼6.2 D(calc.) = 6.202 Optical Properties: Transparent to nearly opaque. Color: Brownish red, red-orange, reddish brown to blackish brown, nearly black. Streak: Orange to brownish red. Luster: Greasy. Optical Class: Biaxial (–), rarely biaxial (+). Pleochroism: Weak to strong; X = Y = canary-yellow to greenish yellow; Z = brownish yellow. Orientation: X = c; Y = b; Z = a. Dispersion: r> v,strong; rarely r< v.α= 2.185(10) β = 2.265(10) γ = 2.35(10) 2V(meas.) = ∼90◦ Cell Data: Space Group: P nma. a = 7.593 b = 6.057 c = 9.416 Z = 4 X-ray Powder Pattern: Venus mine, [El Guaico district, C´ordobaProvince,] Argentina; close to mottramite. 3.23 (vvs), 5.12 (vs), 2.90 (vs), 2.69 (vsb), 2.62 (vsb), 1.652 (vs), 4.25 (s) Chemistry: (1) (2) (1) (2) SiO2 0.02 ZnO 19.21 10.08 As2O5 0.00 PbO 55.47 55.30 +350◦ V2O5 22.76 22.53 H2O 2.17 −350◦ FeO trace H2O 0.02 MnO trace H2O 2.23 CuO 0.56 9.86 Total 100.21 100.00 (1) Abenab, Namibia. -
B Clifford Frondel
CATALOGUE OF. MINERAL PSEUDOMORPHS IN THE AMERICAN MUSEUM -B CLIFFORD FRONDEL BU.LLETIN OF THEAMRICANMUSEUM' OF NA.TURAL HISTORY. VOLUME LXVII, 1935- -ARTIC-LE IX- NEW YORK Tebruary 26, 1935 4 2 <~~~~~~~~~~~~~7 - A~~~~~~~~~~~~~~~, 4~~~~~~~~~~~~~~~~~~~~~~~~~~~~~4 4 4 A .~~~~~~~~~~~~~~~~~~~~~~~~~~4- -> " -~~~~~~~~~4~~. v-~~~~~~~~~~~~~~~~~~t V-~ ~~~~~~~~~~~~~~~~ 'W. - /7~~~~~~~~~~~~~~~~~~~~~~~~~~7 7-r ~~~~~~~~~-A~~~~ ~ ~ ~ ~ ~ ~ ~ ~ ~ -'c~ ~ ~ ' -7L~ ~ ~ ~ ~ 7 54.9:07 (74.71) Article IX.-CATALOGUE OF MINERAL PSEUDOMORPHS IN THE AMERICAN MUSEUM OF NATURAL HISTORY' BY CLIFFORD FRONDEL CONTENTS PAGE INTRODUCTION .................. 389 Definition.389 Literature.390 New Pseudomorphse .393 METHOD OF DESCRIPTION.393 ORIGIN OF SUBSTITUTION AND INCRUSTATION PSEUDOMORPHS.396 Colloidal Origin: Adsorption and Peptization.396 Conditions Controlling Peptization.401 Volume Relations.403 DESCRIPTION OF SPECIMENS.403 INTRODUCTION DEFINITION.-A pseudomorph is defined as a mineral which has the outward form proper to another species of mineral whose place it has taken through the action of some agency.2 This precise use of the term excludes the regular cavities left by the removal of a crystal from its matrix (molds), since these are voids and not solids,3 and would also exclude those cases in which organic material has been replaced by quartz or some other mineral because the original substance is here not a mineral. The general usage of the term is to include as pseudomorphs both petrifactions and molds, and also: (1) Any mineral change in which the outlines of the original mineral are preserved, whether this surface be a euhedral crystal form or the irregular bounding surface of an embedded grain or of an aggregate. (2) Any mineral change which has been accomplished without change of volume, as evidenced by the undistorted preservation of an original texture or structure, whether this be the equal volume replacement of a single crystal or of a rock mass on a geologic scale. -
Lead Sequestration in the Soil Environment with an Emphasis on the Chemical Thermodynamics Involving Phosphate As a Soil Amendment: Review and Simulations
International Journal of Applied Agricultural Research ISSN 0973-2683 Volume 13, Number 1 (2018) pp. 9-19 © Research India Publications http://www.ripublication.com Lead Sequestration in the Soil Environment with an Emphasis on the Chemical Thermodynamics Involving Phosphate as a Soil Amendment: Review and Simulations Michael Aide* and Indi Braden Department of Agriculture, Southeast Missouri State University, USA. (*Corresponding author) Abstract Soil lead (Pb2+) contamination is a global issue and in many instances the extent of the impact is intense. In Missouri (USA) the legacy of lead mining and processing has resulted in widespread soil impact. We present a review of lead research focusing on the use of phosphate soil amendments to reduce the biological availability of lead and to illustrate how simulations of soil solution chemistry may guide researchers in defining their experimental designs. We demonstrate (i) the simulation of lead hydrolysis arising from the dissolution of galena and pyromorphite, (ii) the simulation of lead hydrolysis and the thermodynamically favored precipitation of lead species across selected pH intervals and (iii) provide activity diagrams showing the stability fields for selected soil chemical environments. Thermodynamic simulations are addressed as an important preparatory process for experimental design development and protocol selection involving field-based research. Keywords: Lead, hydrolysis, ion-pair formation, pyromorphite, galena. INTRODUCTION In the eastern Ozarks of Missouri (USA), Mississippi Valley Type lead ores occur in Paleozoic carbonate rock as galena (PbS), with sphalerite (ZnS) and pyrite (FeS2) as important auxiliary minerals [1]. On a world-wide basis, lead (Pb2+) abundances vary with the rock type, ranging from 10 to 40 mg Pb kg-1 in felsic and argillaceous sediments [2]. -
Mottramite, Descloizite, and Vanadinite) in the Caldbeck Area of Cumberland
289 New occurrences of vanadium minerals (mottramite, descloizite, and vanadinite) in the Caldbeck area of Cumberland. By ART~VR W. G. KINGSBURu F.G.S., Dept. of Geology and Mineralogy, University Museum, Oxford, and J. HARTLnY, B.Sc., F.G.S., Dept. of Geology, University of Leeds. [Taken as read 10 June 1954.] Summary.--Four new occurrences of vanadium minerals are described. New X-ray powder data are given for descloizite and mottramite, and show appreciable differences. Evidence is brought that the original occurrence of mottramite was not at Mottram St. Andrew, Cheshire, but Pim Hill, Shropshire, and that most if not all specimens labelled Mottram St. Andrew or Cheshire really came from Pim Hill. ANADIUM minerals are rare in the British Isles, and only two V species, mottramite (Cu, Zn)PbV0tOH and vanadinite Pbs(VO4)aC1, have so far been recorded from a limited number of localities. We do not include the vanadiferous nodules from Budleigh Salterton in Devon, as the vanadiferous mineral has not been identified. Mottramite, supposedly from Mottram St. Andrew in Cheshire, was first described in 1876,1 but we have evidence (below, p. 293) that the locality was in fact Pim Hill in Shropshire. ~ Vanadinite has so far only been found at Leadhills and Wanlockhead in Scotland. Vauquelinite has been de- scribed from Leadhills and Wanlockhead,a but the specimens have since been shown to be mottramite. 4 As a result of our investigations in the Lake District, we have found several new localities in the Caldbeck area for raottramite, deseloizite, and vanadinite. Higher part of Brandy Gill, Carroek Fell. -
Raman Spectroscopic Study of the Mixed Anion Sulphate-Arsenate Mineral Parnauite Cu9[(OH)10|SO4|(Aso4)2].7H2O
QUT Digital Repository: http://eprints.qut.edu.au/ This is the post-print, accepted version of this paper. Published as: Frost, Ray L. and Cejka, Jiri and Keeffe, Eloise C. and Sejkora, Jiri (2009) Raman spectroscopic study of the mixed anion sulphate-arsenate mineral parnauite Cu9[(OH)10|SO4|(AsO4)2].7H2O. Journal of Raman Spectroscopy, 40(11). pp. 1546-1550. © Copyright 2009 John Wiley & Sons, Ltd. Raman spectroscopic study of the mixed anion sulphate-arsenate mineral parnauite . Cu9[(OH)10|SO4|(AsO4)2] 7H2O Ray L. Frost 1 • Jiří Sejkora, 2 Jiří Čejka 1, 2 and Eloise C. Keeffe 1 1 Inorganic Materials Research Program, School of Physical and Chemical Sciences, Queensland University of Technology, GPO Box 2434, Brisbane Queensland 4001, Australia. 2 National Museum, Václavské náměstí 68, CZ-115 79 Praha 1, Czech Republic. The mixed anion mineral parnauite Cu9[(OH)10|SO4|(AsO4)2] 7H2O has been studied by Raman spectroscopy. Characteristic bands associated with arsenate, sulphate, hydroxyl units are identified. Broad bands are observed and are resolved into component bands. Two intense bands at 859 -1 3- and 830 cm are assigned to the ν1 (AsO4) symmetric stretching and ν3 3- (AsO4) antisymmetric stretching modes. The comparatively sharp band at -1 2- 976 cm is assigned to the ν1 (SO4) symmetric stretching mode and a broad -1 2- spectral profile centered upon 1097 cm is attributed to the ν3 (SO4) antisymmetric stretching mode. A comparison of the Raman spectra is made with other arsenate bearing minerals such as carminite, clinotyrolite, kankite, tilasite and pharmacosiderite. KEYWORDS: parnauite, strashimirite, arsenate minerals, Raman spectroscopy, sulphate, hydroxyl, molecular water • Author to whom correspondence should be addressed ([email protected]) 1 INTRODUCTION Parnauite Cu9(AsO4)2(SO4)(OH)10·7H2O is an uncommon mixed anion mineral containing both sulphate and arsenate 1-3 .The mineral is probably orthorhombic with point group 2/m 2/m 2/m 4.