Metazeunerite Cu(UO2)2(Aso4)2 • 8H2O C 2001-2005 Mineral Data Publishing, Version 1 Crystal Data: Tetragonal
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The Structure and Composition of the Mineral Pharmacosiderite
Zeitschrift fUr Kristallographie, Bd. 125, S. 92-108 (1967) The structure and composition of the mineral pharmacosiderite By M. J. BUERGER, W. A. DOLLASE* and ISABEL GARAYCOCHEA-WITTKE** Massachusetts Institute of Technology, Cambridge, Massachusetts Dedicated to Prof. Dr. G. Menzer on the occasion of his 70th birthday (Received April 17, 1967) Auszug Eine Struktur von Pharmakosiderit wurde von ZEMANN 1947 vorgeschlagen. An einem Pharmakosiderit von Cornwall untersuchten wir die Struktur von neuem. Obwohl die starken Reflexe mit P43m bei a = 7,98 A im Einklang sind, in Ubereinstimmung mit ZEMANNS Ergebnissen, verlangen doch einige schwa- chere Reflexe eine groJ3ere Elementarzelle, was zusammen mit einer schwachen Doppelbrechung auf eine geringere Symmetrie hinweist. Wegen der Inhomogeni- tat des Materials muJ3ten wir uns auf die Untersuchung einer gemittelten Struk- tur, bezogen auf eine isometrische Zelle mit a = 7,98 A, beschranken. Wir konn- ten die Struktur bis zu R = 6!% verfeinern. Unsere Untersuchung bestatigt das von ZEMANN vorgeschlagene Strukturgerust, andert jedoch etwas an der Aus- fUllung der offenen Raume, an der keine Alkaliatome beteiligt sind. Wenn die Struktur auf die isometrische Zelle mit a = 7,98 A bezogen wird, so konnen die Wassermolekiile nur teilweise die Punktlagen besetzen, denen sie zugeordnet sind. Wir schlieJ3en daraus, daJ3 das Pharmakosiderit-Gerust kontinuierlich ist, das Wasser in den Hohlraumen jedoch die Symmetrie verringert, und daJ3 sich der einheitlich erscheinende Kristall in Wirklichkeit aus Bereichen zusanunen- setzt, in denen die Anordnung der Wassermolekule einheitlich ist, aber an den Bereichsgrenzen Zwillingsorientierungen aufweist. Es wird gezeigt, daJ3 bei Behandlung von Pharmakosiderit mit Alkalihydro- xyd-Losungen Alkaliatome in die Struktur eindringen. -
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 -
Liroconite Cu2al(Aso4)(OH)4 • 4H2O C 2001-2005 Mineral Data Publishing, Version 1
Liroconite Cu2Al(AsO4)(OH)4 • 4H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. Typically as crystals with a flattened octahedral or lenticular aspect, dominated by {110} and {011} and striated parallel to their intersections, also {001}, {010}, {100}, to 3.6 cm, alone and in sub-parallel groups. May be granular, massive. Physical Properties: Cleavage: On {110}, {011}, indistinct. Fracture: Uneven to conchoidal. Hardness = 2–2.5 D(meas.) = 2.94–3.01 D(calc.) = [3.03] Optical Properties: Transparent to translucent. Color: Sky-blue, bluish green, verdigris-green, emerald-green; pale blue to pale bluish green in transmitted light. Streak: Pale blue to pale green. Luster: Vitreous to resinous. Optical Class: Biaxial (–). Orientation: Y = b; Z ∧ a =25◦. Dispersion: r< v,moderate. α = 1.612(3) β = 1.652(3) γ = 1.675(3) 2V(meas.) = n.d. 2V(calc.) = 72(5)◦ Cell Data: Space Group: I2/a. a = 12.664(2) b = 7.563(2) c = 9.914(3) β =91.32(2)◦ Z=4 X-ray Powder Pattern: Cornwall, England. 6.46 (10), 3.01 (10), 5.95 (9), 2.69 (6), 3.92 (5), 2.79 (5), 2.21 (5) Chemistry: (1) (2) P2O5 3.73 As2O5 23.05 26.54 Al2O3 10.85 11.77 Fe2O3 0.98 CuO 36.38 36.73 H2O 25.01 24.96 Total 100.00 100.00 • (1) Cornwall, England. (2) Cu2Al(AsO4)(OH)4 4H2O. Occurrence: A rare secondary mineral in the oxidized zone of some copper deposits. Association: Olivenite, chalcophyllite, clinoclase, cornwallite, strashimirite, malachite, cuprite, “limonite”. -
Iidentilica2tion and Occurrence of Uranium and Vanadium Identification and Occurrence of Uranium and Vanadium Minerals from the Colorado Plateaus
IIdentilica2tion and occurrence of uranium and Vanadium Identification and Occurrence of Uranium and Vanadium Minerals From the Colorado Plateaus c By A. D. WEEKS and M. E. THOMPSON A CONTRIBUTION TO THE GEOLOGY OF URANIUM GEOLOGICAL S U R V E Y BULL E TIN 1009-B For jeld geologists and others having few laboratory facilities.- This report concerns work done on behalf of the U. S. Atomic Energy Commission and is published with the permission of the Commission. UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1954 UNITED STATES DEPARTMENT OF THE- INTERIOR FRED A. SEATON, Secretary GEOLOGICAL SURVEY Thomas B. Nolan. Director Reprint, 1957 For sale by the Superintendent of Documents, U. S. Government Printing Ofice Washington 25, D. C. - Price 25 cents (paper cover) CONTENTS Page 13 13 13 14 14 14 15 15 15 15 16 16 17 17 17 18 18 19 20 21 21 22 23 24 25 25 26 27 28 29 29 30 30 31 32 33 33 34 35 36 37 38 39 , 40 41 42 42 1v CONTENTS Page 46 47 48 49 50 50 51 52 53 54 54 55 56 56 57 58 58 59 62 TABLES TABLE1. Optical properties of uranium minerals ______________________ 44 2. List of mine and mining district names showing county and State________________________________________---------- 60 IDENTIFICATION AND OCCURRENCE OF URANIUM AND VANADIUM MINERALS FROM THE COLORADO PLATEAUS By A. D. WEEKSand M. E. THOMPSON ABSTRACT This report, designed to make available to field geologists and others informa- tion obtained in recent investigations by the Geological Survey on identification and occurrence of uranium minerals of the Colorado Plateaus, contains descrip- tions of the physical properties, X-ray data, and in some instances results of chem- ical and spectrographic analysis of 48 uranium arid vanadium minerals. -
THE SINGLE-CRYSTAL X-RAY STRUCTURES of BARIOPHARMACOSIDERITE-C, BARIOPHARMACOSIDERITE-Q and NATROPHARMACOSIDERITE
1477 The Canadian Mineralogist Vol. 48, pp. 1477-1485 (2010) DOI : 10.3749/canmin.48.5.1477 THE SINGLE-CRYSTAL X-RAY STRUCTURES OF BARIOPHARMACOSIDERITE-C, BARIOPHARMACOSIDERITE-Q and NATROPHARMACOSIDERITE SIMON L. HAGER, PETER LEVERETT§ AND PETER A. WILLIAMS School of Natural Sciences, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797, Australia STUART J. MILLS Department of Earth and Ocean Sciences, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada DavID E. HIBBS School of Pharmacy, University of Sydney, Sydney, NSW 2006, Australia MATI RAUDSEPP Department of Earth and Ocean Sciences, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada ANTHONY R. KAMPF Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, California 90007, USA WILLIAM D. BIRCH Geosciences Section, Museum Victoria, GPO Box 666, Melbourne, Victoria 3001, Australia ABSTRACT The crystal structures of two polymorphic forms of bariopharmacosiderite have been determined. Bariopharmacosiderite-C, from Robinson’s Reef, Clunes, Victoria, Australia, (Ba0.47K0.04Na0.02)(Fe3.97Al0.03)[(As0.72P0.28)O4]3(OH)4•2.52H2O, is cubic, space group P43m, a 7.942(1) Å, Z = 1, R = 0.089. Bariopharmacosiderite-Q, from the Sunny Corner mine, Sunny Corner, New South Wales, Australia, Ba0.5Fe4(OH)4(AsO4)3•6.16H2O, is tetragonal, space group P42m, a 7.947(1), c 8.049(2) Å, Z = 1, R = 0.050. In the cubic polymorph, Ba ions are disordered over all faces of the unit cell, whereas in the tetragonal polymorph, Ba ions are centered on the 001 face. -
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(?), -
New Mineral Names*
American Mineralogist, Volume 96, pages 1654–1661, 2011 New Mineral Names* PAULA C. PIILONEN,1,† RALPH ROWE,1 GLENN POIRIER,1 AND KIMBERLY T. TAIT2 1Mineral Sciences Division, Canadian Museum of Nature, P.O. Box 3443, Station D, Ottawa, Ontario K1P 6P4, Canada 2Department of Natural History, Royal Ontario Museum,100 Queen’s Park, Toronto, Ontario M5S 2C6, Canada NEW MINERALS The streak is white and the Mohs hardness is estimated to be about 1½. Thin crystal fragments are flexible, but not elastic. The fracture is irregular and there are three cleavage directions: {001} AFMITE* perfect, {010} and {110} good. The mineral is non-fluorescent A.R. Kampf, S.J. Mills, G.R Rossman, I.M. Steele, J.J. Pluth, under all wavelengths of ultraviolet radiation. The density mea- sured by sink-float in aqueous solution of sodium polytungstate and G. Favreau (2011) Afmite, Al3(OH)4(H2O)3(PO4) is 2.39(3) g/cm3. The calculated density, based on the empirical (PO3OH)·H2O, a new mineral from Fumade, Tarn, France: de- 3 scription and crystal structure. Eur. J. Mineral., 23, 269–277. formula and single-crystal cell, is 2.391 g/cm and that for the ideal formula is 2.394 g/cm3. Afmite is found at Fumade, Castelnau-de-Brassac, Tarn, Electron microprobe analyses provided Al2O3 40.20 and France (43°39′30″N, 2°29′58″E). The phosphates occur in P2O5 38.84 wt% and CHN analyses provided H2O 25.64 wt%, fractures and solution cavities in shale/siltstone exposed in total 103.68 wt%. -
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. -
Journal of the Russell Society, Vol 4 No 2
JOURNAL OF THE RUSSELL SOCIETY The journal of British Isles topographical mineralogy EDITOR: George Ryba.:k. 42 Bell Road. Sitlingbourn.:. Kent ME 10 4EB. L.K. JOURNAL MANAGER: Rex Cook. '13 Halifax Road . Nelson, Lancashire BB9 OEQ , U.K. EDITORrAL BOARD: F.B. Atkins. Oxford, U. K. R.J. King, Tewkesbury. U.K. R.E. Bevins. Cardiff, U. K. A. Livingstone, Edinburgh, U.K. R.S.W. Brai thwaite. Manchester. U.K. I.R. Plimer, Parkvill.:. Australia T.F. Bridges. Ovington. U.K. R.E. Starkey, Brom,grove, U.K S.c. Chamberlain. Syracuse. U. S.A. R.F. Symes. London, U.K. N.J. Forley. Keyworth. U.K. P.A. Williams. Kingswood. Australia R.A. Howie. Matlock. U.K. B. Young. Newcastle, U.K. Aims and Scope: The lournal publishes articles and reviews by both amateur and profe,sional mineralogists dealing with all a,pecI, of mineralogy. Contributions concerning the topographical mineralogy of the British Isles arc particularly welcome. Not~s for contributors can be found at the back of the Journal. Subscription rates: The Journal is free to members of the Russell Society. Subsc ription rates for two issues tiS. Enquiries should be made to the Journal Manager at the above address. Back copies of the Journal may also be ordered through the Journal Ma nager. Advertising: Details of advertising rates may be obtained from the Journal Manager. Published by The Russell Society. Registered charity No. 803308. Copyright The Russell Society 1993 . ISSN 0263 7839 FRONT COVER: Strontianite, Strontian mines, Highland Region, Scotland. 100 mm x 55 mm. -
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 66, pages 1274-1280, 1981 NEW MINERAL NAMES* MICHAEL FLEISCHER AND LOUIS J. CABRI Cyanophillite* ar~ 3.350(50)(110), 3.:208(50)(020), 3.080 (80)(111), 2.781(100) (221,111), 2.750(70)(112), 1.721 (60). Kurt Walenta (1981) Cyanophillite, a new mineral from the Clara ~olor1ess to white, luster vitreous. Cleavages {010}, {OOI}, Mine, near Oberwolfach, Central Black Forest. Chem. der {OIl} good, not easily observed. Hardness about 5. Optically Erde, 40, 195-200 (in German). biaxial positive, ns ex= 1.713, /3 = 1.730, )' = 1.748, 2V +88° (89° Analyses gave CuO 36.3, 32.5; Ah03 8.5, -; Sb203 36.5, 38.3; calc.). Material with Zn:Mg = 1:1 is biaxial, neg., ns. ex= 1.689, H20 19.8; sum 101.1%, corresponding to 10CuO . 2Ah03 . 3Sb2 /3 = 1.707, )' = 1.727, 2V ~ 85°. 03 . 25H20. The mineral is dissolved readily by cold 1:1 HCI, The mineral occurs as coatings and small crystals, largest partly dissolved by 1: 1 HN03. Loss of weight when heated (%) dimension about 1 mm; on prosperite, adamite, and austinite 110° 3.4, 150° 9.5, 200° 19.8%. At 250° the mineral is decomposed from Tsumeb, Namibia. Forms observed {010}, {001}, {Oil}, also and turns black. {IOO}very small. X-ray study shows the mineral to be orthorhombic, space The name is for Robert I. Gait, Curator of Mineralogy, Royal group Pmmb, a = 11.82, b = 10.80, c = 9.64A, Z = 1, D 3.10 Ontario Museum, Toronto. Type material is at the Royal Ontario meas., 3.12 calc.