Textural and Compositional Characteristics of Cobalt Ores from the Skuterud Mines of Modum, Norway
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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 -
DOGAMI MP-20, Investigations of Nickel in Oregon
0 C\1 a: w a.. <( a.. en ::::> 0 w z <( __j __j w () en � INVESTIGATIONS OF NICKEL IN OREGON STATE OF OREGON DEPARTMENT OF GEOL.OGY AND MINERAL. IN OUSTRIES DONAL.D .A HUL.L. STATE GEOLOGIST 1978 STATE OF OREGON DEPARTMENT OF GEOLOGY AND MINERAL INDUSTRIES 1069 State Office Building, Portland, Oregon 97201 MISCELLANEOUS PAPER 20 INVESTIGATIONS OF NICKEL IN OREGON Len Ramp, Resident Geologist Grants Pass Field Office Oregon Department of Geology and Mineral Industries Conducted in conformance with ORS 516.030 . •. 5 1978 GOVERNING BOARD Leeanne MacColl, Chairperson, Portland Talent Robert W. Doty STATE GEOLOGIST John Schwabe Portland Donald A. Hull CONTENTS INTRODUCTION -- - ---- -- -- --- Purpose and Scope of this Report Acknowledgments U.S. Nickel Industry GEOLOGY OF LATERITE DEPOSITS - -- - 3 Previous Work - - - - --- 3 Ultramafic Rocks - ----- --- 3 Composition - - -------- - 3 Distribution ------ - - - 3 Structure - 3 Geochemistry of Nickel ---- 4 Chemical Weathering of Peridotite - - 4 The soi I profile ------- 5 M i nero I ogy -- - ----- 5 Prospecting Guides and Techniques- - 6 OTHER TYPES OF NICKEL DEPOSITS - - 7 Nickel Sulfide Deposits- - - - - - 7 Deposits in Oregon 7 Other areas --- 8 Prospecting techniques 8 Silica-Carbonate Deposits - -- 8 DISTRIBUTION OF LATERITE DEPOSITS - ------ 9 Nickel Mountain Deposits - - ------ --------- 9 Location --------------- --- 9 Geology - ------- ----- 11 Ore deposits ----------- - -- 11 Soil mineralogy - ------- 12 Structure --- ---- ---- 13 Mining and metallurgy ------------ ---- 13 Production- -
Nickeline Nias C 2001-2005 Mineral Data Publishing, Version 1
Nickeline NiAs c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Hexagonal. Point Group: 6/m 2/m 2/m. Commonly in granular aggregates, reniform masses with radial structure, and reticulated and arborescent growths. Rarely as distorted, horizontally striated, {1011} terminated crystals, to 1.5 cm. Twinning: On {1011} producing fourlings; possibly on {3141}. Physical Properties: Fracture: Conchoidal. Tenacity: Brittle. Hardness = 5–5.5 VHN = n.d. D(meas.) = 7.784 D(calc.) = 7.834 Optical Properties: Opaque. Color: Pale copper-red, tarnishes gray to blackish; white with strong yellowish pink hue in reflected light. Streak: Pale brownish black. Luster: Metallic. Pleochroism: Strong; whitish, yellow-pink to pale brownish pink. Anisotropism: Very strong, pale greenish yellow to slate-gray in air. R1–R2: (400) 39.2–45.4, (420) 38.0–44.2, (440) 36.8–43.5, (460) 36.2–43.2, (480) 37.2–44.3, (500) 39.6–46.4, (520) 42.3–48.6, (540) 45.3–50.7, (560) 48.2–52.8, (580) 51.0–54.8, (600) 53.7–56.7, (620) 55.9–58.4, (640) 57.8–59.9, (660) 59.4–61.3, (680) 61.0–62.5, (700) 62.2–63.6 Cell Data: Space Group: P 63/mmc. a = 3.621(1) c = 5.042(1) Z = 2 X-ray Powder Pattern: Unknown locality. 2.66 (100), 1.961 (90), 1.811 (80), 1.071 (40), 1.328 (30), 1.033 (30), 0.821 (30) Chemistry: (1) (2) Ni 43.2 43.93 Co 0.4 Fe 0.2 As 55.9 56.07 Sb 0.1 S 0.1 Total 99.9 100.00 (1) J´achymov, Czech Republic; by electron microprobe, corresponds to (Ni0.98Co0.01 Fe0.01)Σ=1.00As1.00. -
Cobalt Mineral Ecology
American Mineralogist, Volume 102, pages 108–116, 2017 Cobalt mineral ecology ROBERT M. HAZEN1,*, GRETHE HYSTAD2, JOSHUA J. GOLDEN3, DANIEL R. HUMMER1, CHAO LIU1, ROBERT T. DOWNS3, SHAUNNA M. MORRISON3, JOLYON RALPH4, AND EDWARD S. GREW5 1Geophysical Laboratory, Carnegie Institution, 5251 Broad Branch Road NW, Washington, D.C. 20015, U.S.A. 2Department of Mathematics, Computer Science, and Statistics, Purdue University Northwest, Hammond, Indiana 46323, U.S.A. 3Department of Geosciences, University of Arizona, 1040 East 4th Street, Tucson, Arizona 85721-0077, U.S.A. 4Mindat.org, 128 Mullards Close, Mitcham, Surrey CR4 4FD, U.K. 5School of Earth and Climate Sciences, University of Maine, Orono, Maine 04469, U.S.A. ABSTRACT Minerals containing cobalt as an essential element display systematic trends in their diversity and distribution. We employ data for 66 approved Co mineral species (as tabulated by the official mineral list of the International Mineralogical Association, http://rruff.info/ima, as of 1 March 2016), represent- ing 3554 mineral species-locality pairs (www.mindat.org and other sources, as of 1 March 2016). We find that cobalt-containing mineral species, for which 20% are known at only one locality and more than half are known from five or fewer localities, conform to a Large Number of Rare Events (LNRE) distribution. Our model predicts that at least 81 Co minerals exist in Earth’s crust today, indicating that at least 15 species have yet to be discovered—a minimum estimate because it assumes that new minerals will be found only using the same methods as in the past. Numerous additional cobalt miner- als likely await discovery using micro-analytical methods. -
Article Is Available On- Bearing Mineralising Event Is Not Possible Because of the Line At
Eur. J. Mineral., 33, 175–187, 2021 https://doi.org/10.5194/ejm-33-175-2021 © Author(s) 2021. This work is distributed under the Creative Commons Attribution 4.0 License. Grimmite, NiCo2S4, a new thiospinel from Príbram,ˇ Czech Republic Pavel Škácha1,2, Jiríˇ Sejkora1, Jakub Plášil3, Zdenekˇ Dolnícekˇ 1, and Jana Ulmanová1 1Department of Mineralogy and Petrology, National Museum, Cirkusová 1740, 193 00 Prague 9 – Horní Pocernice,ˇ Czech Republic 2Mining Museum Príbram,ˇ Hynka Klickyˇ place 293, 261 01 Príbramˇ VI, Czech Republic 3Institute of Physics ASCR, v.v.i., Na Slovance 1999/2, 182 21 Prague 8, Czech Republic Correspondence: Pavel Škácha ([email protected]) Received: 25 December 2020 – Revised: 2 March 2021 – Accepted: 8 March 2021 – Published: 19 April 2021 Abstract. The new mineral grimmite, NiCo2S4, was found in siderite–sphalerite gangue at the dump of shaft no. 9, one of the mines in the abandoned Príbramˇ uranium and base-metal district, central Bohemia, Czech Republic. The new mineral occurs as rare idiomorphic to hypidiomorphic grains up to 200 µm × 70 µm in size or veinlet aggregates. In reflected light, grimmite is creamy grey with a pinkish tint. Pleochroism, polarising colours and internal reflections were not observed. Reflectance values of grimmite in the air (R %) are 42.5 at 470 nm, 45.9 at 546 nm, 47.7 at 589 nm and 50.2 at 650 nm). The empirical formula for grimmite, based on electron-microprobe analyses (n D 13), is Ni1:01(Co1:99Fe0:06Pb0:01Bi0:01/62:07S3:92. The ideal formula is NiCo2S4; requires Ni 19.26, Co 38.67, and S 42.07; and totals 100.00 wt %. -
The Opaque Mineralogy of Metasedimentary Rocks of the Meguma Group, Beaverbank-Rawdon Area, Nova Scotia S
Document généré le 2 oct. 2021 11:42 Atlantic Geology The opaque mineralogy of metasedimentary rocks of the Meguma Group, Beaverbank-Rawdon area, Nova Scotia S. J. Haysom, R. J. Horne et G. Pe-Piper Volume 33, numéro 3, fall 1997 URI : https://id.erudit.org/iderudit/ageo33_3err01 Aller au sommaire du numéro Éditeur(s) Atlantic Geoscience Society ISSN 0843-5561 (imprimé) 1718-7885 (numérique) Découvrir la revue Citer ce document Haysom, S. J., Horne, R. J. & Pe-Piper, G. (1997). The opaque mineralogy of metasedimentary rocks of the Meguma Group, Beaverbank-Rawdon area, Nova Scotia. Atlantic Geology, 33(3), 67–68. All rights reserved © Atlantic Geology, 1997 Ce document est protégé par la loi sur le droit d’auteur. L’utilisation des services d’Érudit (y compris la reproduction) est assujettie à sa politique d’utilisation que vous pouvez consulter en ligne. https://apropos.erudit.org/fr/usagers/politique-dutilisation/ Cet article est diffusé et préservé par Érudit. Érudit est un consortium interuniversitaire sans but lucratif composé de l’Université de Montréal, l’Université Laval et l’Université du Québec à Montréal. Il a pour mission la promotion et la valorisation de la recherche. https://www.erudit.org/fr/ A tlantic Geology 249 ERRATUM The opaque mineralogy of metasedimentary rocks of the Meguma Group, Beaverbank-Rawdon area, Nova Scotia S. J. Haysom1, R.J. Home2 and G. Pe-Piper1 1 Department of Geology, Saint M ary’s University, Halifax, Nova Scotia B3H 3C 3, Canada 2Nova Scotia Department of Natural Resources, P.O. Box 698, Halifax, Nova Scotia B3J 2 T9, Canada Date Received January 15, 1996 Date Accepted June 13, 1997 (Ref.: 1997. -
The Opaque Mineralogy of Metasedimentary Rocks of the Meguma Group, Beaverbank-Rawdon Area, Nova Scotia
A tlantic G eology 105 The opaque mineralogy of metasedimentary rocks of the Meguma Group, Beaverbank-Rawdon area, Nova Scotia S.J. Haysom1, RJ. Horne2 and G. Pe-Piper1 departm ent of Geology, Saint Mary’s University, Halifax, Nova Scotia B3H 3C 3, Canada 2Nova Scotia Department of Natural Resources, P.O. Box 698, Halifax, Nova Scotia B3J 2 T9, Canada Date Received January 15, 1996 Date Accepted June 13, 1997 Opaque mineralogy of a representative cross-section of deformed and metamorphosed turbiditic slate and metasandstone of the Meguma Group has been investigated optically and by electron microprobe. A strong strati graphic control over the presence and abundance of certain opaque minerals is recognized, -which may prove useful for environmental evaluation such as acid drainage potential. Abundant pyrite and pyrrhotite in the lower Halifax Formation reflect concentration of early diagenetic pyrite resulting from the reduction of seawater sulphate under anoxic conditions. Magnetite is restricted to the Goldenville Formation. Ilmenite and rutile occur through out the succession, and minor chalcopyrite, arsenopyrite, covellite, hematite and glaucodot were also noted. Pyrrhotite and ilmenite, as well as spessartine, chlorite and chloritoid porphyroblasts, developed during pro grade metamorphism before and/or during cleavage formation, which also resulted in removal of early diagenetic pyrite. Later pyrite formed by replacement or remobilization of pyrrhotite during retrograde metamorphism. Colloform pyrite, arsenopyrite and chalcopyrite are the youngest mineral phases. On a dtudid la structure mindralogique opaque d’un echantillon representatif de mdtagres et d’ardoise turbiditique deformes et metamorphises du groupe de Meguma, optiquement ainsi qu’a l’aide d’une microsonde dlectronique. -
54 SKUTTERUDITE FROX{ COBALT. ONTARIOI on Some Specimens
54 THE AMENICAN M]NENALOGIST SKUTTERUDITE FROX{ COBALT. ONTARIOI T. I/. WALKER Uruiuersily oJ Torontn On somespecimens recently obtained from the Temiskaming mine, Cobalt, Ontario, small brilliant crystals resembling smal- tite were observed,imbedded in fragments of soft chloritic or micaceouscountry rock includedin the vein. As is well known, smaltite and chloanthite closelyresemble one another and are commonlyintergrown in the samecrystal. It was with a view to determiningthe relative purity of the supposedsmaltite that this examinationwas undertaken. The principal ore in the vein is smaltite,usually massive, but occasionallyforming rough crystalsup to b or 6 millimeters in diameter. The rest of the vein matter is either calcite or lrag- ments of country rock. The small crystals under investigation seemto representthe latest mineral to form;they are tirr white, and verSzlustrous. The specific gravity, determined on 0.62 gram of carefully selectedcrystals, is 6.29,which is closerto the value usually given for skutterudite (CoAss) than to that for smaltite (CoAsz). The crystals, which seldom exceed a millimeter in diameter, were measured on a Goldschmidt goniometer. The fol- lowing forms were obseryed on each crystal: a(IOO), o(111), d(110), and n(211). The relative development of the forms is shown in figure 1. Nothing observed suggests that the crystals are Frc.1. hemihedral-the faces of the last two formswere not alwayspresent in full, but the omissionsappeared to be quite irregular. These four forms have all been observed on both smaltite and skutterudite. An analysis made on the powdered mineral is shown in I. l Presented at the firrt annual meeting of the Mineralogical Society of America, December 28, 1920. -
Cobalt, Nickel and Selenium in Tasmanian Ore Minerals
COBALT, NICKEL ANU SELENIUM IN TASMANIAN ORE MINERALS by G. D. LOFTUS-HILLS, B.Sc. (lions.) Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy. UNIVERSITY OF TASMANIA HOBART 1968 This thesis contains no material which has been accepted for the award of any other degree or diploma in any University and, to the best of my knowledge and belief, contains no copy or paraphrase of material previously published or written by another person, except where due reference is made in the text of the thesis. G. D. LOFTUS-HILLS. University of Tasmania, November, 1968, ABSTRACT Analyses of Co, Ni and Se in pyrites and other minerals from a wide variety of Tasmanian ore deposits support a genetic relationship between the Mt. Lyell (pyritic - Cu) and Rosebery (banded In-Pb-Cu) deposits, and the Cambrian eugeosynclinal volcanic rocks in which they occur. The concentration trends for all the ores due to fundamental availability contain smaller-scale components due to depositional processes, which, except in one case, do not interfere with these trends. The components include impoverishment of Co (and Ni) during remobilization of sulphides, increase in Ni and decrease in Co away from the centre of zoned deposits, impoverishment of Ni (and Co) in replacement as compared with vein lodes, and regular and irregular partitioning of respectively Co-Ni and Se between coexisting minerals. The trends of Co-Ni in pyrite due to availability include the following: (a) The sedimentary-diagenetic pyrites generally contain Co/Ni < 0.5, but show no correlation of Co-Ni values with rock type, age, or degree of recrystallization. -
A Specific Gravity Index for Minerats
A SPECIFICGRAVITY INDEX FOR MINERATS c. A. MURSKyI ern R. M. THOMPSON, Un'fuersityof Bri.ti,sh Col,umb,in,Voncouver, Canad,a This work was undertaken in order to provide a practical, and as far as possible,a complete list of specific gravities of minerals. An accurate speciflc cravity determination can usually be made quickly and this information when combined with other physical properties commonly leads to rapid mineral identification. Early complete but now outdated specific gravity lists are those of Miers given in his mineralogy textbook (1902),and Spencer(M,i,n. Mag.,2!, pp. 382-865,I}ZZ). A more recent list by Hurlbut (Dana's Manuatr of M,i,neral,ogy,LgE2) is incomplete and others are limited to rock forming minerals,Trdger (Tabel,l,enntr-optischen Best'i,mmungd,er geste,i,nsb.ildend,en M,ineral,e, 1952) and Morey (Encycto- ped,iaof Cherni,cal,Technol,ogy, Vol. 12, 19b4). In his mineral identification tables, smith (rd,entifi,cati,onand. qual,itatioe cherai,cal,anal,ys'i,s of mineral,s,second edition, New york, 19bB) groups minerals on the basis of specificgravity but in each of the twelve groups the minerals are listed in order of decreasinghardness. The present work should not be regarded as an index of all known minerals as the specificgravities of many minerals are unknown or known only approximately and are omitted from the current list. The list, in order of increasing specific gravity, includes all minerals without regard to other physical properties or to chemical composition. The designation I or II after the name indicates that the mineral falls in the classesof minerals describedin Dana Systemof M'ineralogyEdition 7, volume I (Native elements, sulphides, oxides, etc.) or II (Halides, carbonates, etc.) (L944 and 1951). -
Primary Minerals of the Jáchymov Ore District
Journal of the Czech Geological Society 48/34(2003) 19 Primary minerals of the Jáchymov ore district Primární minerály jáchymovského rudního revíru (237 figs, 160 tabs) PETR ONDRU1 FRANTIEK VESELOVSKÝ1 ANANDA GABAOVÁ1 JAN HLOUEK2 VLADIMÍR REIN3 IVAN VAVØÍN1 ROMAN SKÁLA1 JIØÍ SEJKORA4 MILAN DRÁBEK1 1 Czech Geological Survey, Klárov 3, CZ-118 21 Prague 1 2 U Roháèových kasáren 24, CZ-100 00 Prague 10 3 Institute of Rock Structure and Mechanics, V Holeovièkách 41, CZ-182 09, Prague 8 4 National Museum, Václavské námìstí 68, CZ-115 79, Prague 1 One hundred and seventeen primary mineral species are described and/or referenced. Approximately seventy primary minerals were known from the district before the present study. All known reliable data on the individual minerals from Jáchymov are presented. New and more complete X-ray powder diffraction data for argentopyrite, sternbergite, and an unusual (Co,Fe)-rammelsbergite are presented. The follow- ing chapters describe some unknown minerals, erroneously quoted minerals and imperfectly identified minerals. The present work increases the number of all identified, described and/or referenced minerals in the Jáchymov ore district to 384. Key words: primary minerals, XRD, microprobe, unit-cell parameters, Jáchymov. History of mineralogical research of the Jáchymov Chemical analyses ore district Polished sections were first studied under the micro- A systematic study of Jáchymov minerals commenced scope for the identification of minerals and definition early after World War II, during the period of 19471950. of their relations. Suitable sections were selected for This work was aimed at supporting uranium exploitation. electron microprobe (EMP) study and analyses, and in- However, due to the general political situation and the teresting domains were marked. -
Spatial Distribution of the Ophiolite-Hosted Co–Ni–As-Rich Hydrothermal Mineralization in the Punta Corna Mining Complex, Lanzo Valleys, Northern Italy
EGU21-7589 https://doi.org/10.5194/egusphere-egu21-7589 EGU General Assembly 2021 © Author(s) 2021. This work is distributed under the Creative Commons Attribution 4.0 License. Spatial distribution of the ophiolite-hosted Co–Ni–As-rich hydrothermal mineralization in the Punta Corna Mining complex, Lanzo Valleys, Northern Italy Giovanni Grieco1, Marilena Moroni1, Micol Bussolesi2, Alessandro Cavallo2, and Simone Orizio1 1Earth Science Department, University of Milan, via S. Botticelli 23, 20133, Milan, Italy 2Department of Earth and Environmental Sciences – DISAT, University of Milan-Bicocca, p.zza della Scienza 1–4, 2016 Milan, Italy Cobalt is a transition metal with a trace element abundance in the Earth’s crust (26.6 ppm). It forms mainly sulfides like carrollite, siegenite and linneite and enters the cobaltite-gersdorffite solid solution and di-tri-arsenides safflorite, rammelsbergite and skutterudite while erythrite and asbolane are secondary Co phases. Cobalt is a Critical Raw Material for the EU, strategically important due to its use in the industry (batteries, superalloys, catalysts etc.). Italy hosts several Co-bearing hydrothermal deposits, which were variably exploited in the past. In this work we focus on the Co-Fe-Ni hydrothermal veins emplaced within the metabasites of the Lanzo Valleys ophiolite complex in the western sector of the Alpine belt. The vein system is collectively called “Punta Corna mining complex”, and was exploited for Fe, Ag and later Co in the past (Castelli et al., 2011, Moroni et al., 2019). A detailed field survey of the past cobalt mining works was carried out in summer 2019, followed by sampling, mostly inside mining tunnels and from waste dumps in order to increase data about this poorly known vein system.