Surface Area and Porosity Determination of Natural Todorokite
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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. -
Jacobsite from the Tamworth District of New South Wales
538 Jacobsite from the Tamworth district of New South Wales. By F .L. STILLWELL, D.Sc., and A. B. EDWAP~DS,D.Sc., Ph.D., D.I.C. Commonwealth Scientific and Industrial Organization, Melbourne. [Taken as read November 2, 1950.] WO new occurrences of the rare manganese mineral jacobsite T (MnF%0~) have come to light in the course of mineragraphic studies carried out as part of the research programme of the Mineragraphic Section of the Commonwealth Scientific and Industrial Research Organization. The jacobsite occurs as a constituent of small bodies of high-grade manganese ore at Weabonga, near Danglemah, and at the Mount Sally mine, about 6 miles west of Danglemah, both in the Tam- worth district of New South Wales. The deposits occur in altered sediments, within a mile or two of a granite contact. 1 They are irregular lenticular veins ranging from a few inches to several feet in thickness, between altered slate walls. The veins do not exceed a length of 200-300 feet. The lode material consists of manganese oxides, chiefly psilomelane and pyrolusite, associated with quartz, rhodonite, and iron oxide. The manganese oxides are mainly supergene, and although the deposits are of high grade near the surface, it is doubtful whether they can be worked below the depths of 50- 60 feet, owing to the increase in the amount of rhodonite and quartz relative to manganese oxides at this depth. In the Weabonga ore the jacobsite occurs as narrow seams and lenticles, about 0.5 cm. across, and 3.0 cm. long enclosed in, and partly replaced by, pyrolusite and psilomelane. -
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 -
Non-Precious Metal Catalysts for Oxygen Reduction Reaction in Alkaline Solutions Zhewen Yin University of South Florida, [email protected]
University of South Florida Scholar Commons Graduate Theses and Dissertations Graduate School March 2018 Non-precious Metal Catalysts for Oxygen Reduction Reaction in Alkaline Solutions Zhewen Yin University of South Florida, [email protected] Follow this and additional works at: http://scholarcommons.usf.edu/etd Part of the Materials Science and Engineering Commons Scholar Commons Citation Yin, Zhewen, "Non-precious Metal Catalysts for Oxygen Reduction Reaction in Alkaline Solutions" (2018). Graduate Theses and Dissertations. http://scholarcommons.usf.edu/etd/7250 This Thesis is brought to you for free and open access by the Graduate School at Scholar Commons. It has been accepted for inclusion in Graduate Theses and Dissertations by an authorized administrator of Scholar Commons. For more information, please contact [email protected]. Non-precious Metal Catalysts for Oxygen Reduction Reaction in Alkaline Solutions by Zhewen Yin A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Materials Science and Engineering Department of Chemical and Biomedical Engineering College of Engineering University of South Florida Co-Major Professor: Venkat R. Bhethanabotla, Ph.D. Co-Major Professor: John N. Kuhn, Ph.D. Scott Campbell, Ph.D. Date of Approval: March 19, 2018 Keywords: Tungsten oxide, Sol-gel processing, Mesoporous, Fuel cells, Electrochemistry Copyright © 2018, Zhewen Yin DEDICATION This work is dedicated to my parents, Mrs. Mei Chen and Mr. Bin Yin, who despite all the sufferings and prolonged separation love me, trust me and have supported me every step of the way. Without their sacrifices and encouragement I could never have walked this far. -
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. -
Development of Novel Biosorbents in Removing Heavy Metals from Aqueous Solution
DEVELOPMENT OF NOVEL BIOSORBENTS IN REMOVING HEAVY METALS FROM AQUEOUS SOLUTION A Thesis Submitted in Fulfilment of the Requirement for the degree of DOCTOR OF PHILOSOPHY IN ENVIRONMENTAL ENGINEERING By Md Anwar Hossain Under the Guidance of Prof. Dr. Huu Hao NGO School of Civil and Environmental Engineering Faculty of Engineering and Information Technology University of Technology, Sydney (UTS) Sydney, Australia December, 2013 Certificate I certify that this thesis has not already been submitted for any degree and is not being submitted as part of candidature for any other degree. I also certify that the thesis has been written by me and any help that I have received in preparing this thesis, and all sources used, have been acknowledged in this thesis. Signature of Candidate …………………………………………………. (Md Anwar Hossain) ii I dedicated this work to my beloved parents Md Akbar Ali Mosa. Ruhila Khatun iii Acknowledgement It was not simple and easy task, but both nerve-racking and enjoyable during my doctoral research at Centre for Technology in Water and Wastewater (CTWW), University of Technology, Sydney (UTS), Australia. It would not have been feasible and possible to achieve this doctoral research without the help and support of the people around me and therefore they need a special mention and thanks here. I would like to appreciate the people for their help and support during my research. My first thanks and gratitude goes to my principal supervisor Prof. Dr. Huu Hao NGO. He was a source of continuous inspiration, motivation, stimulation and strength throughout my research. I would like to show my deep gratitude to my co-supervisors Dr Wenshan GUO, Dr. -
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. -
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. -
Magyar Tudomány
Magyar Tudomány Az élet keletkezése A Világegyetem fejlõdése A jóléti állam – válság és kiutak Doktori iskolák Magyar Akkreditációs Bizottság 2003•101217 Magyar Tudomány • 2003/10 A MAGYAR TUDOMÁNYOS AKADÉMIA FOLYÓIRATA. ALAPÍTÁS ÉVE: 1840 CIX. kötet – Új folyam, XLVIII. kötet, 2003/10. szám Fôszerkesztô: CSÁNYI VILMOS Vezetô szerkesztô: ELEK LÁSZLÓ Olvasószerkesztô: MAJOROS KLÁRA Szerkesztôbizottság: ÁDÁM GYÖRGY, BENCZE GYULA, CZELNAI RUDOLF, CSÁSZÁR ÁKOS, ENYEDI GYÖRGY, KOVÁCS FERENC, KÖPECZI BÉLA, LUDASSY MÁRIA, NIEDERHAUSER EMIL, SOLYMOSI FRIGYES, SPÄT ANDRÁS, SZENTES TAMÁS, VÁMOS TIBOR A lapot készítették: CSAPÓ MÁRIA, CSATÓ ÉVA, GAZDAG KÁLMÁNNÉ, HALMOS TAMÁS, MATSKÁSI ISTVÁN, PERECZ LÁSZLÓ, SPERLÁGH SÁNDOR, SZABADOS LÁSZLÓ, SZENTGYÖRGYI ZSUZSA, F. TÓTH TIBOR Lapterv, tipográfia: MAKOVECZ BENJAMIN Szerkesztôség: 1051 Budapest, Nádor utca 7. • Telefon/fax: 3179-524 [email protected] • www.matud.iif.hu Kiadja az Akaprint Kft. • 1115 Bp., Bártfai u. 65. Tel.: 2067-975 • [email protected] Elôfizethetô a FOK-TA Bt. címén (1134 Budapest, Gidófalvy L. u. 21.); a Posta hírlapüzleteiben, az MP Rt. Hírlapelôfizetési és Elektronikus Posta Igazgatóságánál (HELP) 1846 Budapest, Pf. 863, valamint a folyóirat kiadójánál: Akaprint Kft. 1115 Bp., Bártfai u. 65. Elôfizetési díj egy évre: 6048 Ft Terjeszti a Magyar Posta és alternatív terjesztôk Kapható az ország igényes könyvesboltjaiban Nyomdai munkák: Akaprint Kft. 25845 Felelõs vezetõ: Freier László Megjelent: 15,35 (A/5) ív terjedelemben HU ISSN 0025 0325 1218 TARTALOM Tanulmányok Szathmáry -
High-Temperature X-Ray Study of the System Fe3o4-Mn3o4
U. S. Department of Commerce Research Paper RP2111 National Bureau of Standards Volume 45, July 1950 Part of the Journal of Research of the National Bureau of Standards High-Temperature X-Ray Study of the System Fe 30 4-Mn30 4 By H. F. McMurdie, Barbara M. Sullivanl and Floyd A. Mauer A series of compositions in the system Fea04-Mna04 was prepared and examined at high temperatures by X-ray diffraction methods. Although Fea04 and Mna0 4 form a con tinuous series of substitutional solid solutions stable at room temperatures, t hose composi tions co ntaining less than 60 percent of Mna04 are cubic, of the spinel type, and the rest are tetragonal. Those compositions t hat are tegragonal at room temperature pass through a two-phase region when heated and acquire the cubic spinel-type structure at high tempera tures. The temperature range of t he t wo-phase (exsei~ n ) region varies with composition. The relation to t hi s system of the mincrals vredenburgite and hausmannite is discussed. I. Introduction :Mason prcpared a series of compounds by co A few years ago, while the oxides of manganese pl'ecipi tating l11Lxtures of the hydroxide of iron were being studied in this laboratory (1] / it was and manganese and heating the precipitate at found that Mn304, on being heated, inverts from approximately 1,200 ° C to obtain the proper the tetragonal structure to a cubic form of the s tate of oxidation. In this way, homogeneous spinel type at 1,170° C . preparations covering the range from 20 to 100 The low temperature form of Mn30 4 (hausman mole percent of Mn30 4 were obtained. -
Jakob Maarten Van Bemmelen (November 3, 1830 Amelo – March 13, 1911 Leiden) and the History of the Theory of Adsorption from Solution
http://www.uni-kiel.de/anorg/lagaly/group/klausSchiver/bemmelen.pdf Please take notice of: (c)Beneke, Lagaly. Don't quote without permission. Jakob Maarten van Bemmelen (November 3, 1830 Amelo – March 13, 1911 Leiden) and the history of the theory of adsorption from solution Klaus Beneke and Gerhard Lagaly Institute of Inorganic Chemistry Christian-Albrechts-University Kiel D-24098 Kiel [email protected] February 2005, modified November 15, 2005 2 Jakob Maarten van Bemmelen (November 3, 1830 Amelo – March 13,1911 Leiden) and the history of the theory of adsorption from solution Van Bemmelen was descented from a family, many of whose members were distinguished in education, law, and statesmanship. Jakob Maarten van Bemmelen was born on November 3, 1830 in Amelo where his father Jan Frans van Bemmelen was headmaster of the grammar school. His mother was Antoinetta Adriana de Kempenaer. His father died in the same year (December 26, 1830) and his family moved to Leiden. On September 13, 1847 he matricultated there as a student. He studied inorganic- and organic chemistry also pharmacy under Professor Antonius Henrik van der Boon Mesch (15.04.1804 Jakob Maarten van Bemmelen Delft - 12.08.1874 Leiden), who had only a primitive laboratory at his disposal, where van Bemmelen made some quantitative inorganic analysis. Van der Boon Mesch studied fermentation, mineralogy, industrial chemistry, construction of voltaic batteries and boiling points of water/alcohol mixtures. In 1852, van Bemmelen was appointed as an assistent in the laboratory of Professor Petrus Jan van Kerckhoff (1813 - 1876) in Groningen. Van Kerckhoff was head of the chemistry institute since 1851.