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Xrd and Tem Studies on Nanophase Manganese
Clays and Clay Minerals, Vol. 64, No. 5, 488–501, 2016. 1 1 2 2 3 XRD AND TEM STUDIES ON NANOPHASE MANGANESE OXIDES IN 3 4 FRESHWATER FERROMANGANESE NODULES FROM GREEN BAY, 4 5 5 6 LAKE MICHIGAN 6 7 7 8 8 S EUNGYEOL L EE AND H UIFANG X U* 9 9 NASA Astrobiology Institute, Department of Geoscience, University of Wisconsin Madison, Madison, 10 À 10 1215 West Dayton Street, A352 Weeks Hall, Wisconsin 53706 11 11 12 12 13 Abstract—Freshwater ferromanganese nodules (FFN) from Green Bay, Lake Michigan have been 13 14 investigated by X-ray powder diffraction (XRD), micro X-ray fluorescence (XRF), scanning electron 14 microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), and scanning 15 transmission electron microscopy (STEM). The samples can be divided into three types: Mn-rich 15 16 nodules, Fe-Mn nodules, and Fe-rich nodules. The manganese-bearing phases are todorokite, birnessite, 16 17 and buserite. The iron-bearing phases are feroxyhyte, goethite, 2-line ferrihydrite, and proto-goethite 17 18 (intermediate phase between feroxyhyte and goethite). The XRD patterns from a nodule cross section 18 19 suggest the transformation of birnessite to todorokite. The TEM-EDS spectra show that todorokite is 19 associated with Ba, Co, Ni, and Zn; birnessite is associated with Ca and Na; and buserite is associated with 20 2+ +2 3+ 20 Ca. The todorokite has an average chemical formula of Ba0.28(Zn0.14Co0.05 21 2+ 4+ 3+ 3+ 3+ 2+ 21 Ni0.02)(Mn4.99Mn0.82Fe0.12Co0.05Ni0.02)O12·nH2O. -
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. -
Infrared and Raman Spectroscopic Characterization of the Silicateв
Journal of Molecular Structure 1042 (2013) 1–7 Contents lists available at SciVerse ScienceDirect Journal of Molecular Structure journal homepage: www.elsevier.com/locate/molstruc Infrared and Raman spectroscopic characterization of the silicate–carbonate mineral carletonite – KNa4Ca4Si8O18(CO3)4(OH,F)ÁH2O ⇑ Ray L. Frost a, , Yunfei Xi a, Ricardo Scholz b, Andrés López a, Fernanda Maria Belotti c a School of Chemistry, Physics and Mechanical Engineering, Science and Engineering Faculty, Queensland University of Technology, GPO Box 2434, Brisbane, Queensland 4001, Australia b Geology Department, School of Mines, Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG 35400-00, Brazil c Federal University of Itajubá, Campus Itabira, Itabira, MG 35903-087, Brazil article info abstract Article history: An assessment of the molecular structure of carletonite a rare phyllosilicate mineral with general chem- Received 28 February 2013 ical formula given as KNa4Ca4Si8O18(CO3)4(OH,F)ÁH2O has been undertaken using vibrational spectros- Received in revised form 19 March 2013 copy. Carletonite has a complex layered structure. Within one period of c, it contains a silicate layer of Accepted 19 March 2013 composition NaKSi O ÁH O, a carbonate layer of composition NaCO Á0.5H O and two carbonate layers Available online 26 March 2013 8 18 2 3 2 of composition NaCa2CO3(F,OH)0.5. À1 2À Raman bands are observed at 1066, 1075 and 1086 cm . Whether these bands are due to the CO m1 Keywords: 3 symmetric stretching mode or to an SiO stretching vibration is open to question. Carletonite Multiple bands are observed in the 300–800 cmÀ1 spectral region, making the attribution of these Carbonate Infrared bands difficult. -
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 -
Studies of the Zeolites Composition of Zeolites of the Natrolite Group and Compositional Relations Among Thomsonites Gonnardites, and Natrolites
r-'1 ~ Q I ~ c lt') ~ r-'1 'JJ ~ Q.) < ~ ~ ......-~ ..,.;;j ~ <z 0 0 Q.) 1-4 rJ:J rJ:J N r-'1 ~ Q.) 0 ~ ..c ~ ~ ~ I r-'1 ~ > ~ 0 I ~ rJ:J 'JJ ..,.;;j Q.) < .....-~ 0 . 1-4 ~ C"-' 0 ~ ..,.;;j ~ 0 r-'1 00 C"-' Foster-STUDIES•. OF THE ZEOLITES-Geological Survey Professional Paper 504-D, E Studies of the Zeolites Composition of Zeolites of the Natrolite Group and Compositional Relations among Thomsonites Gonnardites, and Natrolites By MARGARET D. FOSTER SHORTER CONTRIBUTIONS TO GENERAL GEOLOGY GEOLOGICAL SURVEY PROFESSIONAL PAPER 504-D, E UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON 1965 UNITED STATES DEPARTMENT OF THE INTERIOR STEWART L. UDALL, Secretory GEOLOGICAL SURVEY Thomas B. Nolan, Director The U.S. Geological Survey Library has cataloged this publication as follows: Foster, Margaret Dorothy, 1895- Studies of the zeolites. D. Composition of zeolites of the natrolite group. E. Compositional relations among thom sonites, gonnardites, and natrolites. Washington, U.S. Govt. Print. Off., 1965. v, 7; iii, 10 p. diagrs., tables. 30 em. (U.S. Geological Survey. Professional paper 504-D, E) Shorter contributions to general geology. Each part also has separate title page. Includes bibliographies. (Continued on next card) Foster, Margaret Dorothy, 1895- Studies of the zeolites. 1965. (Card 2) 1. Zeolites. I. Title. II. Title: Composition of zeolites of the natro lite group. III. Title: Compositional relations among thomsonites, gonnardites, and natrolites. (Series) For sale by the Superintendent of Documents, U.S. Government Printing Office Washington, D.C. 20402 - Price 25 cents (paper cover) Studies of the Zeolites Composition of Zeolites of the N atrolite Group By MARGARET D. -
Alphab Etical Index
ALPHAB ETICAL INDEX Names of authors are printed in SMALLCAPITALS, subjects in lower-case roman, and localities in italics; book reviews are placed at the end. ABDUL-SAMAD, F. A., THOMAS, J. H., WILLIAMS, P. A., BLASI, A., tetrahedral A1 in alkali feldspar, 465 and SYMES, R. F., lanarkite, 499 BORTNIKOV, N. S., see BRESKOVSKA, V. V., 357 AEGEAN SEA, Santorini I., iron oxide mineralogy, 89 Boulangerite, 360 Aegirine, Scotland, in trachyte, 399 BRAITHWAITE, R. S. W., and COOPER, B. V., childrenite, /~kKERBLOM, G. V., see WILSON, M. R., 233 119 ALDERTON, D. H. M., see RANKIN, A. H., 179 Braunite, mineralogy and genesis, 506 Allanite, Scotland, 445 BRESKOVSKA, V. V., MOZGOVA, N. N., BORTNIKOV, N. S., Aluminosilicate-sodalites, X-ray study, 459 GORSHKOV, A. I., and TSEPIN, A. I., ardaite, 357 Amphibole, microstructures and phase transformations, BROOKS, R. R., see WATTERS, W. A., 510 395; Greenland, 283 BULGARIA, Madjarovo deposit, ardaite, 357 Andradite, in banded iron-formation assemblage, 127 ANGUS, N. S., AND KANARIS-SOTIRIOU, R., autometa- Calcite, atomic arrangement on twin boundaries, 265 somatic gneisses, 411 CANADA, SASKATCHEWAN, uranium occurrences in Cree Anthophyllite, asbestiform, morphology and alteration, Lake Zone, 163 77 CANTERFORD, J. H., see HILL, R. J., 453 Aragonite, atomic arrangements on twin boundaries, Carbonatite, evolution and nomenclature, 13 265 CARPENTER, M. A., amphibole microstructures, 395 Ardaite, Bulgaria, new mineral, 357 Cassiterite, SW England, U content, 211 Arfvedsonite, Scotland, in trachyte, 399 Cebollite, in kimberlite, correction, 274 ARVlN, M., pumpellyite in basic igneous rocks, 427 CHANNEL ISLANDS, Guernsey, meladiorite layers, 301; ASCENSION ISLAND, RE-rich eudialyte, 421 Jersey, wollastonite and epistilbite, 504; mineralization A TKINS, F. -
Petrology of Nepheline Syenite Pegmatites in the Oslo Rift, Norway: Zr and Ti Mineral Assemblages in Miaskitic and Agpaitic Pegmatites in the Larvik Plutonic Complex
MINERALOGIA, 44, No 3-4: 61-98, (2013) DOI: 10.2478/mipo-2013-0007 www.Mineralogia.pl MINERALOGICAL SOCIETY OF POLAND POLSKIE TOWARZYSTWO MINERALOGICZNE __________________________________________________________________________________________________________________________ Original paper Petrology of nepheline syenite pegmatites in the Oslo Rift, Norway: Zr and Ti mineral assemblages in miaskitic and agpaitic pegmatites in the Larvik Plutonic Complex Tom ANDERSEN1*, Muriel ERAMBERT1, Alf Olav LARSEN2, Rune S. SELBEKK3 1 Department of Geosciences, University of Oslo, PO Box 1047 Blindern, N-0316 Oslo Norway; e-mail: [email protected] 2 Statoil ASA, Hydroveien 67, N-3908 Porsgrunn, Norway 3 Natural History Museum, University of Oslo, Sars gate 1, N-0562 Oslo, Norway * Corresponding author Received: December, 2010 Received in revised form: May 15, 2012 Accepted: June 1, 2012 Available online: November 5, 2012 Abstract. Agpaitic nepheline syenites have complex, Na-Ca-Zr-Ti minerals as the main hosts for zirconium and titanium, rather than zircon and titanite, which are characteristic for miaskitic rocks. The transition from a miaskitic to an agpaitic crystallization regime in silica-undersaturated magma has traditionally been related to increasing peralkalinity of the magma, but halogen and water contents are also important parameters. The Larvik Plutonic Complex (LPC) in the Permian Oslo Rift, Norway consists of intrusions of hypersolvus monzonite (larvikite), nepheline monzonite (lardalite) and nepheline syenite. Pegmatites ranging in composition from miaskitic syenite with or without nepheline to mildly agpaitic nepheline syenite are the latest products of magmatic differentiation in the complex. The pegmatites can be grouped in (at least) four distinct suites from their magmatic Ti and Zr silicate mineral assemblages. -
Apophyllite-(Kf)
December 2013 Mineral of the Month APOPHYLLITE-(KF) Apophyllite-(KF) is a complex mineral with the unusual tendency to “leaf apart” when heated. It is a favorite among collectors because of its extraordinary transparency, bright luster, well- developed crystal habits, and occurrence in composite specimens with various zeolite minerals. OVERVIEW PHYSICAL PROPERTIES Chemistry: KCa4Si8O20(F,OH)·8H20 Basic Hydrous Potassium Calcium Fluorosilicate (Basic Potassium Calcium Silicate Fluoride Hydrate), often containing some sodium and trace amounts of iron and nickel. Class: Silicates Subclass: Phyllosilicates (Sheet Silicates) Group: Apophyllite Crystal System: Tetragonal Crystal Habits: Usually well-formed, cube-like or tabular crystals with rectangular, longitudinally striated prisms, square cross sections, and steep, diamond-shaped, pyramidal termination faces; pseudo-cubic prisms usually have flat terminations with beveled, distinctly triangular corners; also granular, lamellar, and compact. Color: Usually colorless or white; sometimes pale shades of green; occasionally pale shades of yellow, red, blue, or violet. Luster: Vitreous to pearly on crystal faces, pearly on cleavage surfaces with occasional iridescence. Transparency: Transparent to translucent Streak: White Cleavage: Perfect in one direction Fracture: Uneven, brittle. Hardness: 4.5-5.0 Specific Gravity: 2.3-2.4 Luminescence: Often fluoresces pale yellow-green. Refractive Index: 1.535-1.537 Distinctive Features and Tests: Pseudo-cubic crystals with pearly luster on cleavage surfaces; longitudinal striations; and occurrence as a secondary mineral in association with various zeolite minerals. Laboratory analysis is necessary to differentiate apophyllite-(KF) from closely-related apophyllite-(KOH). Can be confused with such zeolite minerals as stilbite-Ca [hydrous calcium sodium potassium aluminum silicate, Ca0.5,K,Na)9(Al9Si27O72)·28H2O], which forms tabular, wheat-sheaf-like, monoclinic crystals. -
Adamsite-(Y), a New Sodium–Yttrium Carbonate Mineral
1457 The Canadian Mineralogist Vol. 38, pp. 1457-1466 (2000) ADAMSITE-(Y), A NEW SODIUM–YTTRIUM CARBONATE MINERAL SPECIES FROM MONT SAINT-HILAIRE, QUEBEC JOEL D. GRICE§ and ROBERT A. GAULT Research Division, Canadian Museum of Nature, P.O. Box 3443, Station D, Ottawa, Ontario K1P 6P4, Canada ANDREW C. ROBERTS Geological Survey of Canada, 601 Booth Street, Ottawa, Ontario K1A 0E8, Canada MARK A. COOPER Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada ABSTRACT Adamsite-(Y), ideally NaY(CO3)2•6H2O, is a newly identified mineral from the Poudrette quarry, Mont Saint-Hilaire, Quebec. It occurs as groups of colorless to white and pale pink, rarely pale purple, flat, acicular to fibrous crystals. These crystals are up to 2.5 cm in length and form spherical radiating aggregates. Associated minerals include aegirine, albite, analcime, ancylite-(Ce), calcite, catapleiite, dawsonite, donnayite-(Y), elpidite, epididymite, eudialyte, eudidymite, fluorite, franconite, gaidonnayite, galena, genthelvite, gmelinite, gonnardite, horváthite-(Y), kupletskite, leifite, microcline, molybdenite, narsarsukite, natrolite, nenadkevichite, petersenite-(Ce), polylithionite, pyrochlore, quartz, rhodochrosite, rutile, sabinaite, sérandite, siderite, sphalerite, thomasclarkite-(Y), zircon and an unidentified Na–REE carbonate (UK 91). The transparent to translucent mineral has a vitreous to pearly luster and a white streak. It is soft (Mohs hardness 3) and brittle with perfect {001} and good {100} and {010} cleav- ␣  ␥ ° ° ages. Adamsite-(Y) is biaxial positive, = V 1.480(4), = 1.498(2), = 1.571(4), 2Vmeas. = 53(3) , 2Vcalc. = 55 and is nonpleochroic. Optical orientation: X = [001], Y = b, Z a = 14° (in  obtuse). It is triclinic, space group P1,¯ with unit-cell parameters refined from powder data: a 6.262(2), b 13.047(6), c 13.220(5) Å, ␣ 91.17(4),  103.70(4), ␥ 89.99(4)°, V 1049.1(5) Å3 and Z = 4. -
Infrare D Transmission Spectra of Carbonate Minerals
Infrare d Transmission Spectra of Carbonate Mineral s THE NATURAL HISTORY MUSEUM Infrare d Transmission Spectra of Carbonate Mineral s G. C. Jones Department of Mineralogy The Natural History Museum London, UK and B. Jackson Department of Geology Royal Museum of Scotland Edinburgh, UK A collaborative project of The Natural History Museum and National Museums of Scotland E3 SPRINGER-SCIENCE+BUSINESS MEDIA, B.V. Firs t editio n 1 993 © 1993 Springer Science+Business Media Dordrecht Originally published by Chapman & Hall in 1993 Softcover reprint of the hardcover 1st edition 1993 Typese t at the Natura l Histor y Museu m ISBN 978-94-010-4940-5 ISBN 978-94-011-2120-0 (eBook) DOI 10.1007/978-94-011-2120-0 Apar t fro m any fair dealin g for the purpose s of researc h or privat e study , or criticis m or review , as permitte d unde r the UK Copyrigh t Design s and Patent s Act , 1988, thi s publicatio n may not be reproduced , stored , or transmitted , in any for m or by any means , withou t the prio r permissio n in writin g of the publishers , or in the case of reprographi c reproductio n onl y in accordanc e wit h the term s of the licence s issue d by the Copyrigh t Licensin g Agenc y in the UK, or in accordanc e wit h the term s of licence s issue d by the appropriat e Reproductio n Right s Organizatio n outsid e the UK. Enquirie s concernin g reproductio n outsid e the term s state d here shoul d be sent to the publisher s at the Londo n addres s printe d on thi s page. -
Chemical Composition and Petrogenetic Implications of Eudialyte-Group Mineral in the Peralkaline Lovozero Complex, Kola Peninsula, Russia
minerals Article Chemical Composition and Petrogenetic Implications of Eudialyte-Group Mineral in the Peralkaline Lovozero Complex, Kola Peninsula, Russia Lia Kogarko 1,* and Troels F. D. Nielsen 2 1 Vernadsky Institute of Geochemistry and Analytical Chemistry, Russian Academy of Sciences, 119991 Moscow, Russia 2 Geological Survey of Denmark and Greenland, 1350 Copenhagen, Denmark; [email protected] * Correspondence: [email protected] Received: 23 September 2020; Accepted: 16 November 2020; Published: 20 November 2020 Abstract: Lovozero complex, the world’s largest layered peralkaline intrusive complex hosts gigantic deposits of Zr-, Hf-, Nb-, LREE-, and HREE-rich Eudialyte Group of Mineral (EGM). The petrographic relations of EGM change with time and advancing crystallization up from Phase II (differentiated complex) to Phase III (eudialyte complex). EGM is anhedral interstitial in all of Phase II which indicates that EGM nucleated late relative to the main rock-forming and liquidus minerals of Phase II. Saturation in remaining bulk melt with components needed for nucleation of EGM was reached after the crystallization about 85 vol. % of the intrusion. Early euhedral and idiomorphic EGM of Phase III crystalized in a large convective volume of melt together with other liquidus minerals and was affected by layering processes and formation of EGM ore. Consequently, a prerequisite for the formation of the ore deposit is saturation of the alkaline bulk magma with EGM. It follows that the potential for EGM ores in Lovozero is restricted to the parts of the complex that hosts cumulus EGM. Phase II with only anhedral and interstitial EGM is not promising for this type of ore. -
Gonnardite Na2caal4si6o20 ² 7H2O C 2001 Mineral Data Publishing, Version 1.2 ° Crystal Data: Tetragonal
Gonnardite Na2CaAl4Si6O20 ² 7H2O c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Tetragonal. Point Group: 42m: Fibrous crystals, at the centers of radiating spherulites, to 3 cm; massive. Physical Properties: Hardness = 5 D(meas.) = 2.25{2.36 D(calc.) = 2.33 Optical Properties: Translucent. Color: White, yellowish to salmon-red. Luster: Silky. Optical Class: Biaxial (+) or ({); commonly zoned. Orientation: X = c. ® = 1.497{1.508 ¯ = 1.498{1.510 ° = 1.499{1.513 2V(meas.) = 50± Cell Data: Space Group: I42d: a = 13.21(1) c = 6.622(4) Z = 2 X-ray Powder Pattern: Chaux de Bergonne, France; may be confused with natrolite and tetranatrolite. 2.92 (100), 5.93 (80), 6.70 (60), 4.44 (60), 4.74 (50), 3.23 (50), 3.12 (40) Chemistry: (1) (2) (3) SiO2 43.45 43.20 44.58 Al2O3 27.91 27.90 25.22 CaO 6.95 3.61 6.94 Na2O 8.69 13.16 7.66 H2O [13.00] 11.74 15.60 Total [100.00] 99.61 100.00 (1) Chaux de Bergonne, France; by electron microprobe, H2O by di®erence; corresponding to Na2:22Ca0:98Al4:32Si5:71O20 ² 5:70H2O: (2) Aci Trezza, Sicily, Italy; corresponds to Na3:5Ca0:5Al4:5 Si5:9O20:8 ² 5:35H2O: (3) Na2CaAl4Si6O20 ² 7H2O: Mineral Group: Zeolite group. Occurrence: In cavities in basalt, leucite tephrite, and altered skarn. Association: Zeolites, calcite. Distribution: Well characterized material from: in France, at Chaux de Bergonne, Gignat, Puy de D^ome. In Italy, from Capo di Bove, near Rome, Lazio; and at Aci Castello, Aci Trezza, Osilo, and other places on Sardinia.