Diamond Dan's Mineral Names Dictionary
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Crystalline Silica, Cristobalite (CAS No
Crystalline Silica, Quartz (CAS No. 14808-60-7) Crystalline Silica, Cristobalite (CAS No. 14464-46-1) Crystalline Silica, Tridymite (CAS No. 15468-32-3) Diatomaceous earth (CAS No. 61790-53-2) This dossier on crystalline silica, quartz, cristobalite and tridymite and diatomaceous earth presents the most critical studies pertinent to the risk assessment of these substances in their use in drilling muds and cement additives. This dossier does not represent an exhaustive or critical review of all available data. The majority of information presented in this dossier was obtained from the ECHA database that provides information on chemicals that have been registered under the EU REACH (ECHA). Where possible, study quality was evaluated using the Klimisch scoring system (Klimisch et al., 1997). For the purpose of this dossier, crystalline silica, quartz (CAS No. 14808-60-7) has been reviewed as representative of crystalline silica cristobalite and tridymite. Crystalline silica, quartz is also considered representative of diatomaceous earth, as they both consist mainly of silicon dioxide. Screening Assessment Conclusion – Crystalline silica, quartz, cristobalite and tridymite and diatomaceous earth are classified as tier 1 chemicals and require a hazard assessment only. 1 BACKGROUND Crystalline silica is a common mineral found in the earth's crust. Materials like sand, stone, concrete and mortar contain crystalline silica. It is also used to make products such as glass, pottery, ceramics, bricks and artificial stone. Silica, in the form of sand, is used as the main ingredient in sand casting for the manufacture of metallic components in engineering and other applications. The high melting point of silica enables it to be used in such applications. -
Phase Equilibria and Thermodynamic Properties of Minerals in the Beo
American Mineralogist, Volwne 71, pages 277-300, 1986 Phaseequilibria and thermodynamic properties of mineralsin the BeO-AlrO3-SiO2-H2O(BASH) system,with petrologicapplications Mlnx D. B.qnroN Department of Earth and SpaceSciences, University of California, Los Angeles,Los Angeles,California 90024 Ansrru,cr The phase relations and thermodynamic properties of behoite (Be(OH)r), bertrandite (BeoSirOr(OH)J, beryl (BerAlrSiuO,r),bromellite (BeO), chrysoberyl (BeAl,Oo), euclase (BeAlSiOo(OH)),and phenakite (BerSiOo)have been quantitatively evaluatedfrom a com- bination of new phase-equilibrium, solubility, calorimetric, and volumetric measurements and with data from the literature. The resulting thermodynamic model is consistentwith natural low-variance assemblagesand can be used to interpret many beryllium-mineral occurTences. Reversedhigh-pressure solid-media experimentslocated the positions of four reactions: BerAlrSiuO,,: BeAlrOo * BerSiOo+ 5SiO, (dry) 20BeAlSiOo(OH): 3BerAlrsi6or8+ TBeAlrOo+ 2BerSiOn+ l0HrO 4BeAlSiOo(OH)+ 2SiOr: BerAlrSiuO,,+ BeAlrOo+ 2H2O BerAlrSiuO,,+ 2AlrSiOs : 3BeAlrOa + 8SiO, (water saturated). Aqueous silica concentrationswere determined by reversedexperiments at I kbar for the following sevenreactions: 2BeO + H4SiO4: BerSiOo+ 2H2O 4BeO + 2HoSiOo: BeoSirO'(OH),+ 3HrO BeAlrOo* BerSiOo+ 5H4Sio4: Be3AlrSiuOr8+ loHro 3BeAlrOo+ 8H4SiO4: BerAlrSiuOrs+ 2AlrSiO5+ l6HrO 3BerSiOo+ 2AlrSiO5+ 7H4SiO4: 2BerAlrSiuOr8+ l4H2o aBeAlsioloH) + Bersio4 + 7H4sio4:2BerAlrsiuors + 14Hro 2BeAlrOo+ BerSiOo+ 3H4SiOo: 4BeAlSiOr(OH)+ 4HrO. -
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 -
Intergrown Emerald Specimen from Chivor Tity Was Confirmed by Raman Spectroscopy
Editor Nathan Renfro Contributing Editors Elise A. Skalwold and John I. Koivula Intergrown Emerald Specimen from Chivor tity was confirmed by Raman spectroscopy. The inclusion exhibited a well-formed hexagonal prismatic shape with Colombia’s Chivor emerald mines are located in the east- pyramid-like termination (figure 2). Although intergrowth ern zone of the Eastern Cordillera range of the Andes emerald crystals have been described and documented in Mountains. Chivor translates to “green and rich land” in the literature several times (G. Grundmann and G. Giu- Chibcha, the language of the indigenous people who were liani, “Emeralds of the world,” in G. Giuliani et al., Eds., already mining emerald more than 500 years ago, before Emeralds of the World, extraLapis English, No. 2, 2002, pp. the arrival of the Spanish conquistadors (D. Fortaleché et al., “The Colombian emerald industry: Winds of change,” Fall 2017 G&G, pp. 332–358). Chivor emeralds exhibit a bright green color with a tint of blue; they have relatively Figure 1. An emerald crystal inclusion measuring high clarity and fewer inclusions than emeralds found in ~2.67 × 2.71 × 5.43 mm is found inside this large Colombia’s western belt. emerald specimen (18.35 × 10.69 × 9.79 mm) from Colombia’s Chivor mine. Photo by John Jairo Zamora. The authors recently examined a rough emerald crystal specimen (figure 1), measuring 18.35 × 10.69 × 9.79 mm, reportedly from Chivor. This crystal weighed 3.22 g (16.10 ct) and had a prismatic hexagonal crystal shape. Standard gemological examination confirmed the gemstone to be emerald, and ultraviolet/visible/near-infrared (UV-Vis-NIR) spectroscopy showed a classic Colombian emerald absorp- tion spectrum. -
New Mineral Names*
American Mineralogist, Volume 68, pages 280-2E3, 1983 NEW MINERAL NAMES* MrcnnBr- FrelscHen AND ADoLF Pnnsr Arsendescloizite* The mineral occurs at Uchucchacua,Peru, in acicular crystals up to 2fi) x 20 microns, associatedwith galena, manganoan (1982) Paul Keller and P. J. Dunn Arsendescloizite, a new sphalerite, pyrite, pyrrhotite, and alabandite, with gangue of mineral from Tsumeb. Mineralog. Record, 13, 155-157. quartz, bustamite, rhodonite, and calcite. Also found at Stitra, pyrite-pyrrhotite in rhyo- Microprobe analysis (HzO by TGA) gave AszOs 26.5, PbO Sweden,in a metamorphosed deposit 52.3,ZnO1E.5, FeO 0.3, Il2O2.9, sum 100.5%,corresponding to litic and dacitic rocks; in roundedgrains up to 50 fl.min diameter, associated with galena, freibergite, gudmundite, manganoan Pb1.s6(Zn1.63Fe6.oJ(AsOaXOH)1a or PbZn(AsO+XOH), the ar- senateanalogue ofdescloizite. The mineral is slightly soluble in sphalerite,bismuth, and spessartine. hot HNO3. The name is for A. Benavides, for his contribution to the Weissenbergand precessionmeasurements show the mineral development of mining in Peru. Type material is at the Ecole (Uchucchacua)and at the Free to be orthorhombic, space group F212121,a : 6.075, b = 9.358, Natl. Superieuredes Mines, Paris (SAtra). c = 7.$44, Z = 4, D. calc. 6.57. The strongestX-ray lines University, Amsterdam, Netherlands M.F. (31 eiven) are 4.23(6)(lll); 3.23(lOXl02);2.88(10)(210,031); 2.60 Kolfanite* (E)(13 I ) ; 2.W6)Q3r) ; I .65(6X33I, 143,233); r.559 (EX3I 3,060,25I ). Crystalsare tabular up to 1.0 x 0.4 x 0.5 mm in size, on {001}, A. -
Erzherzog Johann Und Sein Gedenkjahr 2009
Erzherzog Johann und sein Gedenkjahr 2009 Diplomarbeit zur Erlangung des akademischen Grades einer Magistra der Philosophie an der Geisteswissenschaftlichen Fakultät der Karl-Franzens-Universität Graz vorgelegt von : Hermine Fürst am Institut für Volkskunde und Kulturanthropologie der Universität Graz Begutachter: Ao. Univ.-Prof. Dr. phil. Helmut Eberhart Graz, 2013 Vorwort Das Thema für meine Diplomarbeit entstand auf der Exkursion zur österreichischen Regionalkultur von Herrn Prof. Dr. Helmut Eberhart im Oktober 2009. Als wir auf der Heimfahrt von Maria Zell am Brandhof vorbeifuhren machte uns Herr Prof. Eberhart auf den ehemaligen landwirtschaftlichen Musterbetrieb von Erzherzog Johann aufmerksam. Nachdem 2009 das Gedenkjahr zum 150. Todestag Erzherzog Johanns stattfand, und ich die Veranstaltungen dazu interessiert beobachtete, wollte ich einfach mehr über diese Person und seine Zeit wissen. So ließ mich das Thema nicht mehr los und es entstand daraus ″Erzherzog Johann und sein Gedenkjahr 2009 ″ Aufrichtigen Dank möchte ich Herrn Univ.-Prof. Dr. Helmut Eberhart aussprechen, der mich auf dieses sehr interessante Thema aufmerksam machte und für die fachliche Betreuung während meiner Arbeit. Ein besonderer Dank gilt auch Fr. Dr. Silvia Renhart der Leiterin des Gedenkjahres zum 150. Todestag von Erzherzog Johann für ihre fachkundige Unterstützung und der Bereitstellung von Unterlagen. Weiters möchte ich mich bei Herrn Dipl.-Ing. Heiner Herzog bedanken, mit dem ich ein sehr interessantes Gespräch führen konnte, sowie bei allen weiteren -
Optical-Spectroscopy.Pdf
Reviews in Mineralogy & Geochemistry Vol. 78 pp. 371-398, 2014 9 Copyright© Mineralogical Society of America Optical Spectroscopy George R. Rossman Division of Geological and Planetary Sciences California Institute of Technology Pasadena, California 91125-2500, U.S.A. grr@ gps.caltech.edu INTRODUCTION Optical spectroscopy is concerned with the measurement of the absorption, reflection and emission of light in the near-ultraviolet (-250 nm) through the mid-infrared ( -3000 nm) portions of the spectrum. The human interface to the geological and mineralogical world is primarily visual. Optical spectroscopy is, in particular, well suited to investigating the origin of color in minerals. The reflection spectroscopy of minerals has been motivated to a large extent by interest in remote sensing. Emission spectra are usually studied in reference to luminescence phenomena. Studies of mineral color, metal ion site occupancy, oxidation states and concentrations have generally been done with absorption spectroscopy. This chapter concentrates on single crystal absorption spectroscopy. Absorption of light by crystals can occur for a number of reasons. For many minerals, the presence of ions of transition elements (e.g., Ti, V, Cr, Mn, Fe, Co, Ni, Cu) in their various oxidation states is the cause of light absorption. In some minerals, the individual ions cause the light absorption while in others it is the interaction between ions such as between Fe2+ and Fe3+ that causes color. In some minerals, rare-earth elements are an important source of color. 2 Some minerals are colored by small molecular units involving metal ions (UOl+, Cr04 -) or anions (S 3- in sodalites). Many sulfide minerals such as cinnabar (HgS) and realgar (As4S4) owe their color to band gaps in the semiconducting sulfides. -
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 -
Cavansite, a Calcium and Vanadium Silicate of Formula Ca(VO)(Si4o1o
.. ,., Cavansite, a calcium and vanadium silicate of formula Ca(VO)(Si4O1o).4H.P, occurs as sky-blue to greenish-blue radiating prismatic rosettes up to~mm in size associated with its dimorph, pentagonite, in a roadcut near Lake Owyhee State Park in Malheur County, Oregon. Discovery of these two minerals is attributed to Mr. and Mrs. Leslie Perrigo of Fruitland, Idaho, (at this locality in 1961), and to Dr. John Cowles at the Goble locality in 1963 (see below). Associated with the cavansite and pentagonite are abundant colorless analcime, stilbite, chabazite, thomsonite and heulandite, as well as colorless to pale yellow calcite, and rare green or colorless apophyllite. This occurence and a similar emplacement (of cavansite only) near Goble, Columbia County, Oregon (co-type localities), represent the only known deposits of these two minerals in the United States. As determined by X-ray fluorescense and crystal stfiucture analysis, cavansite is orthorhombic, conforms to space group Pcmn (D2h 6), has a unit cell with a=lO.298(4), b=l3.999(7), c=9.6O1(2) Angstroms, contains four formula units, is optically biaxial positive and strongly pleochroic. Pentagonite, the dimorph, occurs as prismatic crystals twinned to form fivelings with a star shaped cross section. Also orthorhombic, it belongs to space group 12 Ccm21(C2v ), and has a unit cell with a=lO.298(4), b=13.999(7), and c=B.891(2) Angstroms, and also contains ··four formula units. The pentagonite crystals are optically very similar to cavansite, but are biaxially negative. The cell dimensions given tend to vary· to a small degree, presumably because of varying zeolitic water content. -
Institute of Mineralogy – Report 2008
Institute of Mineralogy – Report 2008 2008 has been a very special year for us. Following more than four years of intense prepara- tions, terra mineralia opened its gates to the public in October with a week of festivities (see also report 2007). Ever since, the steady stream of visitors from near and afar has already lured more than 50,000 people to the exhibits, and Freiberg is more lively than ever. With the successful filling of the chair of Mineral Resources and Petrology with Dr. Jens Gutzmer (be- fore: University of Johannesburg, RSA), our house is finally complete again and all three groups back to full strength. Shortly before the end of the year, the working group Applied and General Mineralogy received a particular honour: Dr. Kristian Ufer was bestowed with the Hans-Joachim-Martini-Award for his works in the “Development of structural models for the Rietveld quantification of swellable illite/smectite minerals in rocks”. This is the solution of a riddle that has been seen as a non-solvable applied problem for many decades. The addi- tional impetus from these successes is already noticeable. The year was much richer, how- ever, and the following pages report about related events and achievements. We should not neglect the sad sides, though. This mainly includes the death of three reputable professors of our institute who have strongly contributed to shaping our house, its reputation and direc- tion. Institute, University and City Contemporary issues in and around Freiberg. Rector (Vice-chancellor) Georg Unland was nominated the new Finance Minister of our Free-state of Saxony. -
Minnesota's Mineral Resources
CHAPTER • 9 Minnesota's Mineral Resources IN MINNESOTA the production of iron ore is far more valuable economically than the total of all other mineral products, but im portant industries are based on Minnesota's other geological forma tions as well. Architectural, monumental, and structural stone are produced from granite, limestone, dolomite, and other Minnesota rocks. Gravel and sand are excavated and processed, and clay is used for many ceramic products. :Manganese in important amounts occurs in the iron ores of the Cuyuna district. Finally, although they are often not thought of as mineral products, two of our most im portant mineral resources are water and soil. The iron ores and mining operations of the Mesabi, Vermilion, and Cuyuna iron-bearing districts and of the southeastern lYlinnesota counties will be discussed in detail in later chapters, but a few sta tistics on Minnesota's iron ore industry may remind us how impor tant this geological heritage is. The following is an estimate of Min nesota's iron ore reserves, made on lYlay 1, 1961: Gross Tons Mesabi Range 500,799,179 Vermilion Range 9,755,974 Cuyuna Range 36,530,000 Fillmore County 'il,860,337 Total iron ore 549,945,490 172 MI NESOTA'S MINERAL RESOURCES The total production of iron ore in Minne ota to January 1, 1962, was 2,529,737,553 tons. Total taxes paid on iron ore to January 1, 1961 , were approximately $1,257,448,400, a very important source of funds for the state government. Slightly over 60 per cent of the total iron ore produced in the United States has come from l\1inne- ota. -
High-Pressure Crystal Chemistry of Beryl (Beralrsi.Otr) and Euclase
American Mineralogist, Volume 71, pages 977-984, 1986 High-pressurecrystal chemistry of beryl (BerAlrSi.Otr) and euclase(BeAlSiO4OH) Rosnnr M. HaznN, ANonpw Y. Au, Llnnv W. FrNcnn GeophysicalLaboratory, CarnegieInstitution of Washington, 2801 Upton Street,N.W., Washington, D.C. 20008 Ansrnlcr Compressibilities and high-pressurecrystal structures of beryl and euclasehave beon determined by X-ray methods at severalpressures. Beryl (hexagonal,space group P6/mcc) has nearly isotropic compressibility; linear compressibilitiesperpendicular and parallel to the c axis ateB':1.72 + 0.04 x l0-a kbar-'and B,:2.10 + 0.09 x 10-akbar-'. The correspondingbulk modulus is 1.70 + 0.05 Mbar if the pressurederivative of the bulk modulus K'is assumedto be 4. Euclase(monoclinic, spacegroup P2r/a)has anisotropic compression,with maximum compressibrlity of 2.44 + 0.05 x l0-a kbar-l parallel to the unique monoclinic b axis, and minimum compressibility of 1.50 + 0.03 x 10-a kbar-' approximately parallel to [01]. The intermediate axis of compressionhas a magnitude of 1.96 + 0.05 x lO-akbar-'in the a-c plane.The bulk modulus of euclaseis 1.59 t 0.03 Mbar if K' is assumedto be 4. The bulk moduli ofBe, Al, and Si cation coordination polyhedrain beryl are all consistent with 1.7 Mbar, which is the crystal bulk modulus. Beryl compressionoccurs primarily by shorteningof cation-anion bond distances.In euclase,the 2.3-Mbar polyhedralbulk moduli are significantly greater than the observed 1.6-Mbar crystal modulus. Compression in euclase,particularly along the b crystallographicaxis, results from a combination of poly- hedral compressionand changesin interpolyhedral angles.