Jacobsite from the Tamworth District of New South Wales
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Redalyc.Mineralogical Study of the La Hueca Cretaceous Iron-Manganese
Revista Mexicana de Ciencias Geológicas ISSN: 1026-8774 [email protected] Universidad Nacional Autónoma de México México Corona Esquivel, Rodolfo; Ortega Gutiérrez, Fernando; Reyes Salas, Margarita; Lozano Santacruz, Rufino; Miranda Gasca, Miguel Angel Mineralogical study of the La Hueca Cretaceous Iron-Manganese deposit, Michoacán, south-western Mexico Revista Mexicana de Ciencias Geológicas, vol. 17, núm. 2, 2000, pp. 142-151 Universidad Nacional Autónoma de México Querétaro, México Available in: http://www.redalyc.org/articulo.oa?id=57217206 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Revista Mexicana de Ciencias Geológicas, volumen 17, número 2, 143 2000, p. 143- 153 Universidad Nacional Autónoma de México, Instituto de Geología, México, D.F MINERALOGICAL STUDY OF THE LA HUECA CRETACEOUS IRON- MANGANESE DEPOSIT, MICHOACÁN, SOUTHWESTERN MEXICO Rodolfo Corona-Esquivel1, Fernando Ortega-Gutiérrez1, Margarita Reyes-Salas1, Rufino Lozano-Santacruz1, and Miguel Angel Miranda-Gasca2 ABSTRACT In this work we describe for the first time the mineralogy and very briefly the possible origin of a banded Fe-Mn deposit associated with a Cretaceous volcanosedimentary sequence of the southern Guerrero terrane, near the sulfide massive volcanogenic deposit of La Minita. The deposit is confined within a felsic tuff unit; about 10 meters thick where sampled for chemical analysis. Using XRF, EDS and XRD techniques, we found besides todorokite, cryptomelane, quartz, romanechite (psilomelane), birnessite, illite-muscovite, cristobalite, chlorite, barite, halloysite, woodruffite, nacrite or kaolinite, and possibly hollandite-ferrian, as well as an amorphous material and two unknown manganese phases. -
Metamorphism of Sedimentary Manganese Deposits
Acta Mineralogica-Petrographica, Szeged, XX/2, 325—336, 1972. METAMORPHISM OF SEDIMENTARY MANGANESE DEPOSITS SUPRIYA ROY ABSTRACT: Metamorphosed sedimentary deposits of manganese occur extensively in India, Brazil, U. S. A., Australia, New Zealand, U. S. S. R., West and South West Africa, Madagascar and Japan. Different mineral-assemblages have been recorded from these deposits which may be classi- fied into oxide, carbonate, silicate and silicate-carbonate formations. The oxide formations are represented by lower oxides (braunite, bixbyite, hollandite, hausmannite, jacobsite, vredenburgite •etc.), the carbonate formations by rhodochrosite, kutnahorite, manganoan calcite etc., the silicate formations by spessartite, rhodonite, manganiferous amphiboles and pyroxenes, manganophyllite, piedmontite etc. and the silicate-carbonate formations by rhodochrosite, rhodonite, tephroite, spessartite etc. Pétrographie and phase-equilibia data indicate that the original bulk composition in the sediments, the reactions during metamorphism (contact and regional and the variations and effect of 02, C02, etc. with rise of temperature, control the mineralogy of the metamorphosed manga- nese formations. The general trend of formation and transformation of mineral phases in oxide, carbonate, silicate and silicate-carbonate formations during regional and contact metamorphism has, thus, been established. Sedimentary manganese formations, later modified by regional or contact metamorphism, have been reported from different parts of the world. The most important among such deposits occur in India, Brazil, U.S.A., U.S.S.R., Ghana, South and South West Africa, Madagascar, Australia, New Zealand, Great Britain, Japan etc. An attempt will be made to summarize the pertinent data on these metamorphosed sedimentary formations so as to establish the role of original bulk composition of the sediments, transformation and reaction of phases at ele- vated temperature and varying oxygen and carbon dioxide fugacities in determin- ing the mineral assemblages in these deposits. -
The Wittelsbach-Graff and Hope Diamonds: Not Cut from the Same Rough
THE WITTELSBACH-GRAFF AND HOPE DIAMONDS: NOT CUT FROM THE SAME ROUGH Eloïse Gaillou, Wuyi Wang, Jeffrey E. Post, John M. King, James E. Butler, Alan T. Collins, and Thomas M. Moses Two historic blue diamonds, the Hope and the Wittelsbach-Graff, appeared together for the first time at the Smithsonian Institution in 2010. Both diamonds were apparently purchased in India in the 17th century and later belonged to European royalty. In addition to the parallels in their histo- ries, their comparable color and bright, long-lasting orange-red phosphorescence have led to speculation that these two diamonds might have come from the same piece of rough. Although the diamonds are similar spectroscopically, their dislocation patterns observed with the DiamondView differ in scale and texture, and they do not show the same internal strain features. The results indicate that the two diamonds did not originate from the same crystal, though they likely experienced similar geologic histories. he earliest records of the famous Hope and Adornment (Toison d’Or de la Parure de Couleur) in Wittelsbach-Graff diamonds (figure 1) show 1749, but was stolen in 1792 during the French T them in the possession of prominent Revolution. Twenty years later, a 45.52 ct blue dia- European royal families in the mid-17th century. mond appeared for sale in London and eventually They were undoubtedly mined in India, the world’s became part of the collection of Henry Philip Hope. only commercial source of diamonds at that time. Recent computer modeling studies have established The original ancestor of the Hope diamond was that the Hope diamond was cut from the French an approximately 115 ct stone (the Tavernier Blue) Blue, presumably to disguise its identity after the that Jean-Baptiste Tavernier sold to Louis XIV of theft (Attaway, 2005; Farges et al., 2009; Sucher et France in 1668. -
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 -
Chromium(III/VI) Binding to Magnetite (Fe3o4), Hausmannite (Mn3o4), and Jacobsite (Mnfe2o4) Nanomaterials
University of Texas at El Paso DigitalCommons@UTEP Open Access Theses & Dissertations 2010-01-01 Chromium(III/VI) Binding To Magnetite (Fe3O4), Hausmannite (Mn3O4), And Jacobsite (Mnfe2O4) Nanomaterials Jeffrey Edward Hernandez University of Texas at El Paso, [email protected] Follow this and additional works at: https://digitalcommons.utep.edu/open_etd Part of the Analytical Chemistry Commons, and the Environmental Sciences Commons Recommended Citation Hernandez, Jeffrey Edward, "Chromium(III/VI) Binding To Magnetite (Fe3O4), Hausmannite (Mn3O4), And Jacobsite (Mnfe2O4) Nanomaterials" (2010). Open Access Theses & Dissertations. 2499. https://digitalcommons.utep.edu/open_etd/2499 This is brought to you for free and open access by DigitalCommons@UTEP. It has been accepted for inclusion in Open Access Theses & Dissertations by an authorized administrator of DigitalCommons@UTEP. For more information, please contact [email protected]. CHROMIUM(III/VI) BINDING TO MAGNETITE (Fe 3O4), HAUSMANNITE (Mn 3O4), AND JACOBSITE (MnFe 2O4) NANOMATERIALS JEFFREY EDWARD HERNANDEZ Department of Chemistry APPROVED: ______________________________ Jorge Gardea-Torresdey, Ph.D. Chair ______________________________ Jose R. Peralta-Videa, Ph.D. ______________________________ Elizabeth J. Walsh, Ph.D. __________________________ Patricia D. Witherspoon, Ph.D. Dean of the Graduate School Copyright © By Jeffrey Edward Hernandez 2010 Dedication To GOD the father almighty To my beloved Beatrice To my mother Margarita, my sister Lorraine and my entire family “Science can purify religion from error and superstition; religion can purify science from idolatry and false absolutes. Each can draw the other into a wider world, a world in which both can flourish.... We need each other to be what we must be, what we are called to be.” Pope John Paul II CHROMIUM(III/VI) BINDING TO MAGNETITE (Fe 3O4), HAUSMANNITE (Mn 3O4), AND JACOBSITE (MnFe 2O4) NANOMATERIALS By JEFFREY HERNANDEZ, B.S. -
Surface Area and Porosity Determination of Natural Todorokite
NATIONAL AND KAPODISTRIAN UNIVERSITY OF ATHENS Surface area and porosity determination of natural todorokite- rich manganese (Mn) oxides, Cape Vani Mn deposit, Milos Island, Greece: implications for potential industrial applications By: Alexandra Stavropoulou A Thesis submitted in partial fullfilment of the requirements for the degree of Master of Science (M.Sc.) in the Faculty of Geology and Geoenvironment Supervisor: Prof. Stephanos P. Kilias January 2017 Master Thesis Stavropoulou V. Alexandra Examination Committee 1. Stephanos Kilias, Professor 2. Athanasios Godelitsas, Associate Professor 3. Ioannis Mitsis, Assistant Professor 2 Master Thesis Stavropoulou V. Alexandra ABSTRACT Natural todorokite-rich Mn oxide ore samples derived from the Cape Vani Mn oxide deposit, Milos Island, Greece, were studied by means of N2 BET specific surface area (SSA), and pore volume measurements. Cape Vani Mn oxide ores occur in a Pliocene- Pleistocene intravolcanic marine basin, they consist primarily of nanocrystalline and crystal defective todorokite, and δ-MnO2, hollandite-cryptomelane-coronadite- manjiroite and pyrolusite that cement volcaniclastic sandstone, and are suggested to be derived from biogenic Mn oxide precursors. Todorokite which possesses many potential technological and industrial applications, has been identified in Cape Vani employing primarily high-resolution transmission electron microscopy (HR-TEM) ; moreover, the Milos todorokite has identical nanoparticle morphology to experimentally produced todorokite from birnessite (Atkins et al., 2014) under conditions analogous to marine diagenetic and hydrothermal settings. The determined SSA and porosity were compared to available relevant data from the published literature, i.e. natural and synthetic todorokite in order to evaluate its industrial and/or environmental application prospects. The measured N2 BET surface areas of the sandstone-hosted Cape Vani material range from 10.7 to 53.1 m2/g, and correspond largely to Mn oxides and primarily todorokite. -
THE MICROHARDNESS of OPAQUE MINERALS VOL.I THESIS Submitted by B.B. YOUNG, B.Sc., A.R.S.M. Degree of Doctor of Philosophy In
THE MICROHARDNESS OF OPAQUE MINERALS VOL.I THESIS Submitted by B.B. YOUNG, B.Sc., A.R.S.M. Degree of Doctor of Philosophy in the Faculty of Science UNIVERSITY OF LONDON April, 1961 Department of Mining Geology, Imperial College, London. I CONTENTS VOL. 1 Page No. Abstracts 1 Acknowledgements 4 Introduction 5 Chapter I. THEORY OF HARDNESS 9 A. General 9 B. Nature of the bonding forces 10 C. Hardness in relation to polishing 14 D. Assessement of hardness 16 E. Microhardness testing instruments 22 Chapter II. EXPERIMENTAL PROCEDURE 25 A. Methods of mounting sections 25 B. Relative merits of the mounting media used 30 C. Grinding and polishing techniques 32 D. Orientation of sections 36 E. Measurement of microhardness 44 F. Routine procedure 42 G. Accuracy and renroducibility of results 45 11 Page No. Chapter III. VARIATION OF MICROHARDNESS WITH LOAD 53 A. Variation of microhardness values with load 53 (a)General 53 (b)Results 60 (c)Discussion of the results 69 (d)Conclusions 77 B. The relation between load and grain size 78 (a)General 78 (b)Discussion 80 C. Variation of the deformation characteristics with load 88 Chapter IV. VARIATION OF MICROHATNESS WITH ORIENTATION 90 A. General 90 B. Microhardness values determined from randomly oriented sections 91 C. The relation, during indentation, between deformation processes and orientation 104 D. Microhardness values obtained on oriented sections of mineral 110 (a)General 110 (b)Discussion of the results 111 (i) Isometric minerals 111 (ii) Tetragonal minerals 130 (iii)Hexagonal mineral 139 iii Page No. (iv) Orthorhombic minerals 150 (v) Monoclinic minerals 163 (vi) Triclinic mineral E. -
Lower Applegate Area
... (26) ELDER MANGANESE LOWER APPLEGATE AREA Rhodonite ore with some rhodochrosite and hard manganese oxides in fracture planes occurs in a black, siliceous, metamorphosed sediment. The rock may be cobbed to show fairly large pieces of deep pink rhodonite. From the standpoint of metallurgical manganese ore, the prospect shows little promise. Authority: FWL (?) Department report Owner: J. R. Elder(?) Location: Sec. 6, T. 39 S., R. 5 W., south of Mungers Creek. Geology: "The rocks of the locality are old, highly metamorphosed sediments." n'l'he only opening -~he deposit is an opencut about 10 ft. long with a face about 8 ft. high, all in a black, siliceous, metamorphosed sediment, into which eydrothermal solutions have penetrated, depositing quartz, rhodonite and a small amount of rhodochrosite in irregular small seams and lenses. A thin\. coating of hard manganese oxides covers some fracture planes, and a little soft black oxide occurs in joint cracks near the surface." "The rock may be cobbed to show fairly large pieces of deep pink rhodonite, and several hundred pounds has been sold to collectors and lapidaries. The work done on the deposit has been to obtain rhodonite for this purpose". "The surface indicttes a considerable area of similar country rock, and probably trenching would show a greuter extent of the rhodonite oc currence. From the standpoint of producing a metallurgical manganese ore, however, the prospect shows little promise." SITE NP.ME: ELDER MANGANESE COUNTY: JOSEPHINE SYNONYMS: OWNER: LOCATION: MINING DIS:LOWER APPLEGATE BLM FS DIS: QUADl: GR.ANTS PASS SCALE: 100000 TOWNSHIP:039S QUAD2: OREGON CAVES SCALE: 62500 R.ANGE:005W RIVER BASIN:17 SECTION:06 PHYSIOG: 13 KLAMATH MOUNTAINS SECT FRACT:S USGS NUM: M013351 LAT:42-12-22N DOGAMI MLR: LONG:123-20-21W REPORTER: LEE, W UTM N:4672500 AFFILIATION: USGS UTM E:472000 REP DATE: 74 01 UTM Z:+10 UPDATE BY: FERNS, MARK L. -
Pink Minerals by Dean Sakabe MEETING Wednesday March 25
MARCH 2015 - VOLUME 50, ISSUE 3 Meeting Times Pink Minerals By Dean Sakabe MEETING Pink Minerals is the theme for March. Please note that will not be talking Wednesday about the Pink Diamonds from the Arglye mine. Nor the Pink Sapphires that March 25, 2015 are coming out of Madagascar, which are Pink Sapphires and not light red Ru- by’s there is a difference and Ruby’s are only red everything else is sapphires. 6:15-8:00 pm Makiki District Park Starting off will be the nice Pink Admin Building Quartz’s. These quartz’s colored by traces of Iron and Titanium are the ones NEXT MONTH found in crystal forms. Not the Rose Blue-Green Minerals Quartz found in massive habits. These quartz’s are found in nice clusters or single crystals most notably from the LAPIDARY Minas Gerais region of Brazil. Every Thursday Pink Quartz, Galileia, Minas Gerais, 6:00-8:30pm Morganite is a Pink Beryl, predomi- Brazil Makiki District Park nately a Beryllium, Aluminum, Silicate 2nd floor Arts and Oxide. It was first identified in 1910, and was named the following year by Crafts Bldg George Kunz. Who named this mineral in honor of J. P. Morgan, who in turn happened to be an avid collec- MEMBERSHIP tor of Gemstones. Morganite DUE COSTS 2015 receives its pink color via Man- Single: $10.00 ganese which substituted itself Family: $15.00 for Aluminum in the crystal lat- tice. © Rock & Mineral Society of Ha- wai`i, Inc. Pink Smithsonite (or Cobal- P.O. Box 23020 toan Smithsonite) is a Zinc Honolulu, HI 96823-3020 Carbonate. -
The Origins of Color in Minerals Four Distinct Physical Theories
American Mineralogist, Volume 63. pages 219-229, 1978 The origins of color in minerals KURT NASSAU Bell Laboratories Murray Hill, New Jersey 07974 Abstract Four formalisms are outlined. Crystal field theory explains the color as well as the fluores- cence in transition-metal-containing minerals such as azurite and ruby. The trap concept, as part of crystal field theory, explains the varying stability of electron and hole color centers with respect to light or heat bleaching, as well as phenomena such as thermoluminescence. The molecular orbital formalism explains the color of charge transfer minerals such as blue sapphire and crocoite involving metals, as well as the nonmetal-involving colors in lazurite, graphite and organically colored minerals. Band theory explains the colors of metallic minerals; the color range black-red-orange- yellow-colorless in minerals such as galena, proustite, greenockite, diamond, as well as the impurity-caused yellow and blue colors in diamond. Lastly, there are the well-known pseudo- chromatic colors explained by physical optics involving dispersion, scattering, interference, and diffraction. Introduction The approach here used is tutorial in nature and references are given for further reading or, in some Four distinct physical theories (formalisms) are instances, for specific examples. Color illustrations of required for complete coverage in the processes by some of the principles involved have been published which intrinsic constituents, impurities, defects, and in an earlier less technical version (Nassau, 1975a). specific structures produce the visual effects we desig- Specific examples are given where the cause of the nate as color. All four are necessary in that each color is reasonably well established, although reinter- provides insights which the others do not when ap- pretations continue to appear even in materials, such plied to specific situations. -
Petrology of Mn Carbonate–Silicate Rocks from the Gangpur Group, India
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by eprints@NML Journal of Asian Earth Sciences 25 (2005) 773–780 www.elsevier.com/locate/jaes Petrology of Mn carbonate–silicate rocks from the Gangpur Group, India B.K. Mohapatraa,*, B. Nayakb aRegional Research Laboratory (CSIR), Bhubaneswar 751 013, India bNational Metallurgical Laboratory (CSIR), Jamshedpur 831 007, India Received 11 April 2003; revised 6 February 2004; accepted 21 July 2004 Abstract Metamorphosed Mn carbonate–silicate rocks with or without oxides (assemblage I) and Mn silicate–oxide rocks with minor Mn carbonate (assemblage II) occur as conformable lenses within metapelites and metacherts of the Precambrian Gangpur Group, India. The petrology of the carbonate minerals: rhodochrosite, kutnahorite, and calcite that occur in these two assemblages is reported. Early stabilisation of spessartine, aegirine, quartz, and carbonates (in a wide solid solution range) was followed by pyroxmangite, tephroite, rhodonite through decarbonation reactions. Subsequently, jacobsite, hematite, braunite, hollandite and hausmannite have formed by decarbonation–oxidation processes during prograde metamorphism. Textural characteristics and chemical composition of constituent phases suggest that the mineral assemblages reflect a complex ! w relationship between protolithic composition, variation of XCO2 ( 0.2 to 0.3) and oxygen fugacity. A variation of XCO2 and fO2 would imply internal buffering of pore fluids through mineral reactions that produced diverse assemblages in the carbonate bearing manganiferous rocks. A minor change in temperature (from around 400 to 450 8C) does not appear to have had any major influence on the formation of different mineral associations. q 2004 Elsevier Ltd.