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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 -
Wickenburgite Pb3caal2si10o27² 3H2O
Wickenburgite Pb3CaAl2Si10O27 ² 3H2O c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Hexagonal. Point Group: 6=m 2=m 2=m: Tabular holohedral crystals, dominated by 0001 and 1011 , to 1.5 mm. As spongy aggregates of small, highly perfect f g f g individuals; as subparallel aggregates or rosettes; granular. Physical Properties: Cleavage: 0001 , indistinct. Tenacity: Brittle but tough. Hardness = 5 D(meas.) = 3.85 D(cfalc.) g= 3.88 Fluoresces dull orange under SW UV. Optical Properties: Transparent to translucent. Color: Colorless to white; rarely salmon-pink. Luster: Vitreous. Optical Class: Uniaxial ({). Dispersion: r < v; moderate. ! = 1.692 ² = 1.648 Cell Data: Space Group: P 63=mmc: a = 8.53 c = 20.16 Z = 2 X-ray Powder Pattern: Near Wickenburg, Arizona, USA. 10.1 (100), 3.26 (80), 3.93 (60), 3.36 (40), 2.639 (40), 5.96 (30), 5.04 (30) Chemistry: (1) (2) SiO2 42.1 40.53 Al2O3 7.6 6.88 PbO 44.0 45.17 CaO 3.80 3.78 H2O 3.77 3.64 Total 101.27 100.00 (1) Near Wickenburg, Arizona, USA. (2) Pb3CaAl2Si10O24(OH)6: [needsnew??formula] Occurrence: In oxidized hydrothermal veins, carrying galena and sphalerite, in quartz and °uorite gangue (near Wickenburg, Arizona, USA). Association: Phoenicochroite, mimetite, cerussite, willemite, crocoite, duftite, hemihedrite, alamosite, melanotekite, luddenite, ajoite, shattuckite, vauquelinite, descloizite, laumontite. Distribution: In the USA, in Arizona, at several localities south of Wickenburg, Maricopa Co., including the Potter-Cramer property, Belmont Mountains, and the Moon Anchor mine; on dumps at a Pb-Ag-Cu prospect in the Artillery Peaks area, Mohave Co.; and in the Dives (Padre Kino) mine, Silver district, La Paz Co. -
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. -
To Volume 55, 1970
THE AMERICAN MINERALOGIST. VOL, 55. NOVEMtsER.DECEMBER. 1970 INDEX TO VOLUME 55, 1970 The index for this volume attempts to combine the advantages of the content of the traditional subject index, with the computer storage and retrieval possibilities of the KWIC index that was used for volumes 52-54. This index is processed and printed from the input to the Bibli.ography and Iniler oJ Geology,under a contract arrangement with the American Geological Institute. Thanks are due them for their excellent cooperation in this initial venture. The content and layout of this index, and in particular the choice of sub- ject headings, and subheadings, is still evolving. General cornments and specific suggestions from users will be welcomed, and should be addressed to the Editor oI The American Mineralogisl. 2147 AUTHOR INDEX TO VOLUME 55 7-8 1440 Adams. John W. A convenient nonoxidizing heating method for metamict minerals tt-12 2141 Ahmed, E. F. R. (ed.) Crystallographiccomputing [book review] 7-8 1302 Akizuki, Mizuhiko. Slip structureof heated sphalerite 3-4 491 Albee, Arden L. Semiquantitative electron microprobe determination of Fer1 /Fer t and Mn:r /Mnr' in oxides and silicatesand its applicationto petrologicproblems 9-r0 1772 Alberti, Alberto. variation in diffractometer profiles of powder with a gaussian dispersionof the chemical composition t-2 299 Allmann, Rudolf. How to recognize O OH-and H:O in crystal structures determined by x-rays [abstr.] Allmann, Rudolf. How to recognize O: , OH', and H:O in crystal structures 5-6 1003 determined by x-rays Anderson, C. P. The crystal structuresof the humite minerals;ll, Chondrodite 7-8 1182 Anderson, Charles A. -
Claringbullite Cu4cl(OH)7 C 2001-2005 Mineral Data Publishing, Version 1
Claringbullite Cu4Cl(OH)7 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Hexagonal. Point Group: 6/m 2/m 2/m. As micaceous or platy crystals, to 1 cm, flattened on {1000}; in groups of divergent plates. Physical Properties: Cleavage: Perfect on {0001}; distinct on {1010} and {1120}. Hardness = Soft. D(meas.) = 3.9 D(calc.) = 3.99 Optical Properties: Transparent to translucent. Color: Blue; pale blue in transmitted light. Luster: Pearly. Optical Class: Uniaxial (–). ω = 1.782 = [1.780] Cell Data: Space Group: P 63/mmc. a = 6.6733(5) c = 9.185(1) Z = 2 X-ray Powder Pattern: Nchanga mine, Zambia or Kambove, Congo. 5.75 (vvs), 2.700 (vvs), 2.445 (vs), 4.89 (s), 4.58 (s), 2.889 (ms), 1.797 (ms) Chemistry: (1) (2) (3) CuO 78.18 74.42 77.85 Cl 8.55 8.30 8.68 H2O [15.14] [19.03] 15.43 SO3 0.06 0.12 −O=Cl2 1.93 1.87 1.96 Total [100.00] [100.00] 100.00 (1) Nchanga mine, Zambia; by electron microprobe, H2O by difference, presence confirmed by elemental analyzer. (2) Kambove, Congo; by electron microprobe, H2O by difference, presence confirmed by elemental analyzer; the mean of five analyses from both localities above corresponds • to Cu8.00(SO4)0.01Cl1.99(OH)14.00 0.68H2O. (3) Cu4Cl(OH)7. Occurrence: In oxidized copper ore or slag, produced under chlorine-rich conditions. Association: Cuprite, malachite, quartz, brochantite, nantokite, paratacamite, connellite, spangolite. Distribution: In the Nchanga mine, Chingola, Zambia. From the M’sesa mine, Kambove, Katanga Province, Congo (Shaba Province, Zaire). -
Mineral Ecology and Network Analysis of Chromium, Platinum
MINERAL ECOLOGY AND NETWORK ANALYSIS OF CHROMIUM, PLATINUM, GOLD AND PALLADIUM A THESIS IN ENVIRONMENTAL AND URBAN GEOSCIENCES Presented to the Faculty of the University Of Missouri-Kansas City in partial fulfillment of The requirements for the degree MASTER OF SCIENCE By CHARLES ANDENGENIE MWAIPOPO B.S., University of Missouri-Kansas City, 2018 Kansas City, Missouri 2020 MINERAL ECOLOGY AND NETWORK ANALYSIS OF CHROMIUM, PLATINUM, GOLD AND PALLADIUM Charles Andengenie Mwaipopo, Candidate for the Master of Science Degree University of Missouri-Kansas City, 2020 ABSTRACT Data collected on the location of mineral species and related minerals from the field have many great uses from mineral exploration to mineral analysis. Such data is useful for further exploration and discovery of other minerals as well as exploring relationships that were not as obvious even to a trained mineralogist. Two fields of mineral analysis are examined in the paper, namely mineral ecology and mineral network analysis through mineral co-existence. Mineral ecology explores spatial distribution and diversity of the earth’s minerals. Mineral network analysis uses mathematical functions to visualize and graph mineral relationships. Several functions such as the finite Zipf-Mandelbrot (fZM), chord diagrams and mineral network diagrams, processed data and provided information on the estimation of minerals at different localities and interrelationships between chromium, platinum, gold and palladium-bearing minerals. The results obtained are important in highlighting several connections that could prove useful in mineral exploration. The main objective of the study is to provide any insight into the relationship among chromium, platinum, palladium and gold that could prove useful in mapping out potential locations of either mineral in the future. -
New Mineral Names
THE AMURICAN MINERALOGIST. VOL. 53, JULY-AUGUST, 1968 NEW MINERAL NAMES Mrcn,lrr- FlBrscunr< Unnamed Lead-Bismuth Telluride J. C. Rucrr.mca (1967) Electron probe studies of some Canadian telluride minerals. (abstr). Can. Mineral.,9, 305. A new Pb-Bi telluride has been found as minute inclusions in chalcopyrite from the Robb Montbray mine, Montbray Township, Quebec.The probable formula is (Pb,Bi)rTe+. J. A. Mondarino Sakuraiite Arrna Karo (1965) Sakuraiite, a new mineral. Chigakw Kenkyu (Earth Sci.mce Studies), Sakurai Vol. 1-5 [in Japanese]. Electron microprobe anaiyses of two grains with different texture gave C:u23j- 2,21 *2;Zn 10+1, 14+1; Fe 9*1, 5+0.5;Ag 4105, 3.5+0.5;ln 17+2,23+2; Sn 9+7, 4+0.5; S 31+3, 30+2; total 103*10.5, 100.5+9.5, correspondingto (Cur pfnsTFenT Ags )(In6 zSnoa)Sr z and (Cur tZno sF'eoaAgs 1)(Inn gSnor)Sr 1 respectively or A:BSa, with A: Cu, Zn, Fe, Ag (Cu ) Zn ) FeAg) and B : In, Sn (In > Sn). This is the indium analogue of kesterite. Spectrographic anaiysis of the ore containing sakuraiite, stannite, sphalerite, chalcopy- rite and quartz gave Cu, ln, Zn, Sn as major, Fe, Ag as subordinate, Bi as minor and Pb, Ga and Cd as trace constituents. The X-ray powder data are very close to those for zincian stannite [L. G. Berry and R. M. Thompson, GeoLSoc. Amer. Mem. 85, 52 53 (1962)l and give 3.15(l}0)(ll2), 1.927 (n)Q2O,O24),1.650(20)(132, 116),2.73(10)(020,004) as the strongest lines. -
Minerals of Arizona Report
MINERALS OF ARIZONA by Frederic W. Galbraith and Daniel J. Brennan THE ARIZONA BUREAU OF MINES Price One Dollar Free to Residents of Arizona Bulletin 181 1970 THE UNIVERSITY OF ARIZONA TUCSON TABLE OF CONT'ENTS EIements .___ 1 FOREWORD Sulfides ._______________________ 9 As a service about mineral matters in Arizona, the Arizona Bureau Sulfosalts ._. .___ __ 22 of Mines, University of Arizona, is pleased to reprint the long-standing booklet on MINERALS OF ARIZONA. This basic journal was issued originally in 1941, under the authorship of Dr. Frederic W. Galbraith, as Simple Oxides .. 26 a bulletin of the Arizona Bureau of Mines. It has moved through several editions and, in some later printings, it was authored jointly by Dr. Gal Oxides Containing Uranium, Thorium, Zirconium .. .... 34 braith and Dr. Daniel J. Brennan. It now is being released in its Fourth Edition as Bulletin 181, Arizona Bureau of Mines. Hydroxides .. .. 35 The comprehensive coverage of mineral information contained in the bulletin should serve to give notable and continuing benefits to laymen as well as to professional scientists of Arizona. Multiple Oxides 37 J. D. Forrester, Director Arizona Bureau of Mines Multiple Oxides Containing Columbium, February 2, 1970 Tantaum, Titanium .. .. .. 40 Halides .. .. __ ____ _________ __ __ 41 Carbonates, Nitrates, Borates .. .... .. 45 Sulfates, Chromates, Tellurites .. .. .. __ .._.. __ 57 Phosphates, Arsenates, Vanadates, Antimonates .._ 68 First Edition (Bulletin 149) July 1, 1941 Vanadium Oxysalts ...... .......... 76 Second Edition, Revised (Bulletin 153) April, 1947 Third Edition, Revised 1959; Second Printing 1966 Fourth Edition (Bulletin 181) February, 1970 Tungstates, Molybdates.. _. .. .. .. 79 Silicates ... -
Charles Palache
NATIONAL ACADEMY OF SCIENCES C H A R L E S P ALACHE 1869—1954 A Biographical Memoir by R E G I N A L D A . D ALY Any opinions expressed in this memoir are those of the author(s) and do not necessarily reflect the views of the National Academy of Sciences. Biographical Memoir COPYRIGHT 1957 NATIONAL ACADEMY OF SCIENCES WASHINGTON D.C. CHARLES PALACHE 1869-1954 BY REGINALD A. DALY ITH EXPERT HELP Charles Palache traced his family tree back Wto the sixteenth century; none of its members seem to have had any leaning toward science. One family of these ancestors belonged to the group of the persecuted Sephardim Jews of Por- tugal who were exiled to Holland. Some of their descendants won distinction as ambassadors to Algiers. Much later, for some un- known reason, one family migrated to Jamaica where Charles Palache's grandfather, John Palache, headed a plantation. For political reasons he abandoned that home in 1834, and put his wife and three daughters on a ship sailing for New York, but he died before he could follow them on the next boat. Three months later Charles Palache's father, James, was born in New York City. At the age of fifteen, James acted as cabin boy on a schooner round- ing Cape Horn and in 1849 landed in San Francisco, his home henceforth. There he married Helen M. Whitney, who had traveled from her home in Green Bay, Wisconsin, to California in a caravan of seven covered wagons. Their son Charles was born in San Fran- cisco on July 18, 1869. -
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Pure Appl. Chem., Vol. 77, No. 3, pp. 643–651, 2005. DOI: 10.1351/pac200577030643 © 2005 IUPAC Solutions in the “big laboratory”: Toward a model for metals at the Earth’s surface* Peter A. Williams School of Science, Food and Horticulture, University of Western Sydney, Locked Bag 1797, Penrith South DC NSW 1797, Australia Abstract: Numerous factors control the chemistry of metal ions in natural aqueous systems. These include the presence of a host of complexing agents, speciation among a variety of competing ligands, buffering due to precipitated solid phases, and the relative influences of kinetic versus thermodynamic phenomena. Natural aqueous systems are inevitably compli- cated, but simple, inorganic models can be constructed to characterize a variety of different environments. While available data sets for these models are large, it is clear that much fur- ther research is required in order to develop more sophisticated models. Some of the fields of research that need to be addressed are outlined, and some of the constraints on such re- search are briefly discussed. Keywords: aqueous solutions; geochemistry; minerals; modeling; equilibria. INTRODUCTION We live in a watery world. The “big laboratory”, the surface of the Earth, is a heterogeneous environ- ment in which aqueous systems play a major role in determining the chemistry of transport of inorganic and organic species. Among other things, the transport of metal ions and their interactions with living organisms is mediated by aqueous chemistries of varying complexity. Understanding such systems is of central importance in many fields ranging from biochemistry, toxicology, and nutrition to hydrometal- lurgy, mineral exploration, and pollution studies [1,2].