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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 -
Theoretical Studies on As and Sb Sulfide Molecules
Mineral Spectroscopy: A Tribute to Roger G. Bums © The Geochemical Society, Special Publication No.5, 1996 Editors: M. D. Dyar, C. McCammon and M. W. Schaefer Theoretical studies on As and Sb sulfide molecules J. A. TOSSELL Department of Chemistry and Biochemistry University of Maryland, College Park, MD 20742, U.S.A. Abstract-Dimorphite (As4S3) and realgar and pararealgar (As4S4) occur as crystalline solids con- taining As4S3 and As4S4 molecules, respectively. Crystalline As2S3 (orpiment) has a layered structure composed of rings of AsS3 triangles, rather than one composed of discrete As4S6 molecules. When orpiment dissolves in concentrated sulfidic solutions the species produced, as characterized by IR and EXAFS, are mononuclear, e.g. ASS3H21, but solubility studies suggest trimeric species in some concentration regimes. Of the antimony sulfides only Sb2S3 (stibnite) has been characterized and its crystal structure does not contain Sb4S6 molecular units. We have used molecular quantum mechanical techniques to calculate the structures, stabilities, vibrational spectra and other properties of As S , 4 3 As4S4, As4S6, As4SIO, Sb4S3, Sb4S4, Sb4S6 and Sb4SlO (as well as S8 and P4S3, for comparison with previous calculations). The calculated structures and vibrational spectra are in good agreement with experiment (after scaling the vibrational frequencies by the standard correction factor of 0.893 for polarized split valence Hartree-Fock self-consistent-field calculations). The calculated geometry of the As4S. isomer recently characterized in pararealgar crystals also agrees well with experiment and is calculated to be about 2.9 kcal/mole less stable than the As4S4 isomer found in realgar. The calculated heats of formation of the arsenic sulfide gas-phase molecules, compared to the elemental cluster molecules As., Sb, and S8, are smaller than the experimental heats of formation for the solid arsenic sulfides, but shown the same trend with oxidation state. -
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 -
A Single-Crystal Epr Study of Radiation-Induced Defects
A SINGLE-CRYSTAL EPR STUDY OF RADIATION-INDUCED DEFECTS IN SELECTED SILICATES A Thesis Submitted to the College of Graduate Studies and Research In Partial Fulfillment of the Requirements For the Degree of Doctor of Philosophy In the Department of Geological Sciences University of Saskatchewan Saskatoon By Mao Mao Copyright Mao Mao, October, 2012. All rights reserved. Permission to Use In presenting this thesis in partial fulfilment of the requirements for a Doctor of Philosophy degree from the University of Saskatchewan, I agree that the Libraries of this University may make it freely available for inspection. I further agree that permission for copying of this thesis in any manner, in whole or in part, for scholarly purposes may be granted by the professor or professors who supervised my thesis work or, in their absence, by the Head of the Department or the Dean of the College in which my thesis work was done. It is understood that any copying or publication or use of this thesis or parts thereof for financial gain shall not be allowed without my written permission. It is also understood that due recognition shall be given to me and to the University of Saskatchewan in any scholarly use which may be made of any material in my thesis. Requests for permission to copy or to make other use of material in this thesis in whole or part should be addressed to: Head of the Department of Geological Sciences 114 Science Place University of Saskatchewan Saskatoon, Saskatchewan S7N5E2, Canada i Abstract This thesis presents a series of single-crystal electron paramagnetic resonance (EPR) studies on radiation-induced defects in selected silicate minerals, including apophyllites, prehnite, and hemimorphite, not only providing new insights to mechanisms of radiation-induced damage in minerals but also having direct relevance to remediation of heavy metalloid contamination and nuclear waste disposal. -
REVISION 1 an Insight at the Inverse Transformation of Realgar Altered By
REVISION 1 An insight at the inverse transformation of realgar altered by light Giovanni Pratesi1,2 and Matteo Zoppi1* 1Museo di Storia Naturale - Sezione Mineralogia e Litologia, Università di Firenze, via La Pira 4, I- 50121 Firenze, Italy. 2Dipartimento di Scienze della Terra, Università di Firenze, via La Pira 4, I-50121 Firenze, Italy. * E-mail: [email protected] ABSTRACT The light-induced alteration of realgar and β-As4S4 is a well known phenomenon but still displays interesting aspects not completely explained. In the transformation from realgar to pararealgar the molecule As4S4 undergoes a structural modification, and ever since the initial studies two important issues have been highlighted: the influence of the oxygen and the reversibility of the process. The previous study on the reversibility of the altered β-As4S4 points out that this polymorph exhibits a dual behaviour. When the light-induced alteration occurs with the presence of the air, pararealgar and arsenolite, along with amorphous material, are the products, while if the air is not present β-As4S4 turns completely into pararealgar. Moreover, when annealing the altered material in the realgar stability fields (220 °C), in the first case pararealgar and amorphous material turn into stoichiometric alacranite, while in the second case the alteration is completely reversible. Similarly, the present study focuses the attention on the question if realgar, when altered by means of the light and when annealed, might behave as β-As4S4 does. These results display that the phenomenon is more complex. The alteration of realgar with the presence of the air yields pararealgar along with arsenolite, a small quantity of uzonite and amorphous material, and when the air is not present pararealgar is the only product. -
Geological Controls on Pit Lake Chemistry: Implications for the Assessment of Water Quality in Inactive Open Pits
IMWA Proceedings 1998 | © International Mine Water Association 2012 | www.IMWA.info Geological Controls on Pit Lake Chemistry: Implications for the assessment of Water Quality in Inactive Open Pits 1 2 2 2 3 R.J.Bowell , J. Barta , M.Gringrich , W.Mansanares and J. Parshley 'Steffen, Robertson & Kirsten (UK) Limited, Stunmit House, 9 Windsor Place, CardiffCFI 3BX, Wales 2Getchell Gold Corporation, Golconda, Nevada NV89414, USA 3Steffen, Robertson & Kirsten (US) Inc., 1755 E. Plumb Lane, Reno, Nevada NV89502, USA ABSTRACT Open pitting is a method of mining used to exploit many mineral commodities. In many instances mining occurs below the water table leading to active dewatering of the pit during mining. On suspension of activity, pumping is terminated and as infilling of the pit is not always economic the pit is flooded, forming a pit lake. Pit Lakes are viewed as a significant environmental issue owing to their visible presence. It is often, erroneously assumed that all pit lakes will be acid and of poor quality. Consequently in many cases extensive water quality modelling is undertaken to determine the chemical characteristics of a pit lake, with only scant geological knowledge of the pit walls. However, the water quality of a mine pit lake is largely predictable from geological knowledge of the ore deposit, the host rocks and mineralogy. In this paper we present a case study from Nevada of an inactive open pit on which a detailed study was conducted to determine the environmental impacts. This study was greatly enhanced by using geological and geochemical mapping of the pit walls in order to determine controls on pit lake chemistry. -
Growth and Raman Spectroscopic Characterization of As4s4 (II) Single Crystals
*4. Manuscript Click here to view linked References Growth and Raman spectroscopic characterization of As4S4 (II) single crystals Atsushi Kyono Division of Earth Evolution Sciences, Graduate School of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai Tsukuba, Ibaraki 305-8572, Japan Corresponding author: A. Kyono Present Address: Geophysical Laboratory, Carnegie Institution of Washington, 5251 Broad Branch Rd. NW, Washington, DC 20015-1305, USA Email: [email protected] Phone: +1-202-478-8940, Fax: +1-202-478-8901 pg. 1 ABSTRACT As described by Kutoglu (1976), single crystals of As4S4 (II) phase have been grown using a new two-step synthesis that drastically increases the reproducibility that is attainable in synthetic experiments. First, through photoinduced phase transformation, pararealgar powder is prepared as a precursor instead of AsS melt. Then it is dissolved and recrystallized from CS2 solvent. Results show that single crystals of the As4S4 (II) phase were obtained reproducibly through the dissolution–recrystallization process. Single crystals of As4S4 (II) obtained using the method were translucent and showed a uniform yellow–orange color. The crystal exhibits a platelet-like shape as a thin film with well-developed faces (0 1 0) and (0 -1 0). The grown crystals are as large as 0.50 × 0.50 × 0.01 mm. They were characterized using powder and single crystal X-ray diffraction techniques to confirm the phase identification and the lattice parameters. The As4S4 (II) phase crystallizes in monoclinic system with cell parameters a = 11.202(4) Å, b = 9.954(4) Å, c = 7.142(4) Å, β = 92.81(4)°, V = 795.4(6) Å3, which shows good agreement with the former value. -
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338 Geologica Macedonica, Vol. 32, No. 2, pp. 95–117 (2018) GEOME 2 IISSN 0352 – 1206 Manuscript received: August 5, 2018 e-ISSN 1857 – 8586 Accepted: November 7, 2018 UDC: 553.46:550.43.08]:504(497.721) 553.497:550.43.08]:504(497.721) Original scientific paper SUPERGENE MINERALOGY OF THE LOJANE Sb-As-Cr DEPOSIT, REPUBLIC OF MACEDONIA: TRACING THE MOBILIZATION OF TOXIC METALS Uwe Kolitsch1,2, Tamara Đorđević2, Goran Tasev3, Todor Serafimovski3, Ivan Boev3, Blažo Boev3 1Mineralogisch-Petrographische Abt., Naturhistorisches Museum, Burgring 7, A-1010 Wien, Austria 2Institut für Mineralogie und Kristallographie, Universität Wien, Althanstr. 14, A-1090 Wien, Austria 3Department of Mineral Deposits, Faculty of Natural and Technical Sciences, “Goce Delčev” University in Štip, Blvd. Goce Delčev 89, 2000 Štip, Republic of Macedonia [email protected] A b s t r a c t: As part of a larger project on the environmental mineralogy and geochemistry of the Lojane Sb- As-Cr deposit, Republic of Macedonia, which was mined for chromite and, later, stibnite until 1979 and is a substantial source of arsenic and antimony pollution, the supergene mineralogy of the deposit was studied. Samples collected on ore and waste dumps were used to identify and characterize the previously uninvestigated suite of supergene mineral phases by standard mineralogical techniques. The following species were determined (in alphabetical order): annaber- gite, arseniosiderite(?), gypsum, hexahydrite, hörnesite, pararealgar, roméite-group minerals, rozenite, scorodite, sen- armontite, stibiconite, sulphur, tripuhyite and valentinite. Their occurrences are described and their local conditions of formation are discussed. High-resolution Raman spectra of hörnesite, hexahydrite and rozenite are provided and com- pared with literature data. -
Franklin-Sterling 2017 Gem and Mineral Show
Franklin-Sterling 2017 GEM & MINERAL SHOW SATURDAY, SEPTEMBER 23rd • 9-5 SUNDAY, SEPTEMBER 24th • 10-4 Littell Community Center FRANKLIN, NEW JERSEY The Fluorescent Mineral Capital of the World Miners Day and Volunteer Appreciation Day, Franklin Mineral Museum, May 7, 2017 Local miners and their families have been honored by the Franklin Mineral Museum for many years. Held on the first Sunday of May, Miners Day also honors museum volunteers. Attendance is by invitation, and the festivities include a buffet lunch, a concert by the famous Franklin Band, and awards to science students in local schools. Mineral collectors and citizens of New Jersey, thank these miners when you see them! They worked to mine our state's zinc and iron ores while recovering the mineral heritage displayed in museums here in Franklin and Sterling Hill, and at many other museums in our country and around the world. These miners worked at the Sterling Mine at Sterling Hill in Ogdensburg, N.J., with the exception of Bob Allen, a veteran of the Scrub Oaks Mine in Mine Hill, N.J. Left to right: Rich Gunderman, Bob Allen, Dick Bostwick (in front), Dom Lorenzo, Tom Laner, Steve Delmar, Mike Hallowich, Paul Rizzo, Andy Gancarcik, Al Restrepo, Chris Auer, Ed Keith, Lenny Talmadge (in back), Bernie Kozykowski, Harvey Barlow (in back), Doug Francisco, and Bill Rude. Sterling Hill miners who were present but missing from both photos are John Antal, Al Grazevich, Mike Gunderman, Ted Hanson, Fred Kirk, Steve Sanford, Henry Wisniewski, and John Yanish. Also present for Miners Day but missing from the photos is Ron Mishkin, who worked at Franklin in the sum- mers of 1952 and 1953, and later in iron mines near Dover. -
Single Crystal Raman Spectroscopy of Selected Arsenite, Antimonite and Hydroxyantimonate Minerals
SINGLE CRYSTAL RAMAN SPECTROSCOPY OF SELECTED ARSENITE, ANTIMONITE AND HYDROXYANTIMONATE MINERALS Silmarilly Bahfenne B.App.Sci (Chem.) Chemistry Discipline This thesis is submitted as part of the assessment requirements of Master of Applied Science Degree at QUT February 2011 KEYWORDS Raman, infrared, IR, spectroscopy, synthesis, synthetic, natural, X-ray diffraction, XRD, scanning electron microscopy, SEM, arsenite, antimonate, hydroxyantimonate, hydrated antimonate, minerals, crystal, point group, factor group, symmetry, leiteite, schafarzikite, apuanite, trippkeite, paulmooreite, finnemanite. i ii ABSTRACT This thesis concentrates on the characterisation of selected arsenite, antimonite, and hydroxyantimonate minerals based on their vibrational spectra. A number of natural arsenite and antimonite minerals were studied by single crystal Raman spectroscopy in order to determine the contribution of bridging and terminal oxygen atoms to the vibrational spectra. A series of natural hydrated antimonate minerals was also compared and contrasted using single crystal Raman spectroscopy to determine the contribution of the isolated antimonate ion. The single crystal data allows each band in the spectrum to be assigned to a symmetry species. The contribution of bridging and terminal oxygen atoms in the case of the arsenite and antimonite minerals was determined by factor group analysis, the results of which are correlated with the observed symmetry species. In certain cases, synthetic analogues of a mineral and/or synthetic compounds isostructural or related to the mineral of interest were also prepared. These synthetic compounds are studied by non-oriented Raman spectroscopy to further aid band assignments of the minerals of interest. Other characterisation techniques include IR spectroscopy, SEM and XRD. From the single crystal data, it was found that good separation between different symmetry species is observed for the minerals studied. -
The Rarer Metals
THE RARER METALS. By FRANK L. HESS. INTRODUCTION. Great gold placer fields, now mere wastes of overturned gravels; worked-out coal fields; exhausted gold, silver, and other mines, with their sterile dumps, gaunt head frames, and decaying shaft houses and mills, testify that, unlike manufactures and agricultural prod ucts, mineral deposits are diminishing assets, and the fact that a large production of some mineral has been made in one year does not necessarily imply that it can be repeated under the impetus of great need. In estimating the possible production of any mineral for any period, a proper weighing of the attending circumstances, the statistics of production of preceding years, and a knowledge of the deposits themselves are all necessary, and these statements probably apply more forcibly to the metals used in alloy steels than to others, for these metals occur in vastly less quantities than coal, iron, copper, or the other common metals, and the individual deposits are smaller' and much less widely distributed and, unlike those of copper or iron, are in very few places concentrated from lean into richer deposits. Comparatively restricted markets and lack of knowledge concern ing these metals themselves and of the minerals in which they occur have prevented prospecting for them until within the last few years, so that as a rule developments of such deposits are small. The subjects briefly discussed here with reference to their avail ability as war supplies are treated more fully in Mineral Resources and other publications of the.United States Geological Survey, espe cially those for recent years. -
Allchar Mineral Assemblage 3
Geologica Macedonica, Vol. 15-16, p. 1-23 (2001-2002) Suppl. GEOME2 SSN 0352 - 1206 Manuscript received: December 15, 200 1 UDC: 553.08 (497 .7) Accepted: March 3, 2002 Original scientific paper ~• ALLCHAR l\1INERAL ASSEMBLAGE l 3 l 4 Blazo Boev , Vladimir Bermanec , Todor Serafimovski\ Sonja Lepitkova , Snezana Mikulcic , 5 5 5 Marin ~oufek\ Gligor Jovanovski , Trajce Stafilov , Metodija Najdoski IDepartment ofPetrology, Mineralogy and Geochemistry, Faculty ofMining and Geology, "Sv. Kiril i Metodij" University, Goce Delcev 89, MK-2000 Stip, Republic ofMacedonia 2Department ofMineral Deposits, Faculty ofMining and Geology, "Sv. Kiril i Metodij" University, Goce Delcev 89, MK-2000 Stip, Republic of Macedonia 3Institute ofMineralogy and Petrology, Department ofGeology, Faculty ofScience, University ofZagreb, Horvatovac bb, HR-JOOOO Zagreb, Croatia 4Department ofMineralogy and Petrology, Croatian Natural History Museum, Demetrova I, HR-JOOOO Zagreb, Croatia 5Institute of Chemistry, Faculty ofScience, "Sv. Kiril i Metodij" University, P.o. Box 162, MK-JOOI Skopje, Republic ofMacedonia Abstract. The paper is a summary of investigatioris carried out on minerals of the Allchar deposit. It discusses the TI-As-Sb-Au mineral ill emblage after detailed and intense research work. Four types of mineralization have been distinguished based on the mineral assemblage present: I. The first ly pe is characterised by high c ment of iron and sulphur, but lower arsenic and thalli um contenl. The pyrite-marcasite mineral assemblage is characterized by the presence of some quantities of arsenic-pyrite. 2. The second type is characterized by the high antimony and low iron and thallium content. Stibnite is the most common mineral in the group.