New Minerals from Lavrion Mining District, Greece
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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 -
Mixite Bicu6(Aso4)3(OH)6 • 3H2O C 2001-2005 Mineral Data Publishing, Version 1 Crystal Data: Hexagonal
Mixite BiCu6(AsO4)3(OH)6 • 3H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Hexagonal. Point Group: 6/m. As acicular crystals, elongated along [0001], commonly in mats, radial fibrous aggregates, or cross-fiber veinlets. Physical Properties: Hardness = 3–4 D(meas.) = 3.79–3.83 D(calc.) = [4.04] Optical Properties: Transparent to translucent. Color: Blue-green to emerald-green, pale green, white; pale green to colorless in transmitted light. Streak: Pale bluish green. Luster: Vitreous, silky in aggregates. Optical Class: Uniaxial (+). Pleochroism: O = colorless; E = bright green. Absorption: E > O. ω = 1.743–1.749 = 1.810–1.830 Cell Data: Space Group: P 63/m. a = 13.646(2) c = 5.920(1) Z = 2 X-ray Powder Pattern: Anton mine, Germany. 12.03 (10), 2.46 (9), 3.57 (8), 2.95 (7), 2.86 (6), 2.70 (6), 2.57 (6) Chemistry: (1) (2) (3) P2O5 1.05 0.06 As2O5 29.51 28.79 29.64 SiO2 0.42 Fe2O3 0.97 Bi2O3 12.25 11.18 20.03 FeO 1.52 CuO 44.23 43.89 41.04 ZnO 2.70 CaO 0.83 0.26 H2O 11.06 11.04 9.29 Total 100.45 99.31 100.00 • (1) J´achymov, Czech Republic. (2) Tintic district, Utah, USA. (3) BiCu6(AsO4)3(OH)6 3H2O. Mineral Group: Mixite group. Occurrence: An uncommon secondary mineral in the oxidized zone of copper deposits. Association: Bismutite, smaltite, bismuth, atelestite, erythrite, malachite, barite. Distribution: From the Geister vein, Werner mine, J´achymov (Joachimsthal), Czech Republic. -
Petersite, a REE and Phosphate Analog of Mixite
American Mineralogist, Volume 67, pages 1039-142, l9E2 Petersite,a REE and phosphateanalog of mixite DoNer-o R. PBecon Department of Geological Sciences University of Michigan Ann Arbor, Michigan 48109 nNn PBIB J. DUNN Department of Mineral Sciences Smithsonian Institution Washington, D.C.20560 Abstract The new mineral petersite (Y,REE,Ca)Cuo@Oa)I(OH)6.3H2O)occurs as a supergene mineral at the traprock quarry at Laurel Hill in Secaucus,New Jersey. It occurs in a brecciatedand mineralizedhornfels near a diabasecontact, in associationwith opal and malachite.Prismatic crystals less than 0. I mm in lengthwith forms {1010}and {0001}occur as radiatingsprays. It is optically uniaxial, positive,with or : 1.666(4) and e: 1.747(4). The measureddensity is 3.41g/cm3. Petersite is hexagonal,probable space group PQlm or P63,with a : 13.288(5)c : 5.877(5)4,V : 898.6(8)43,and Z:2.The strongestlines in the powderdiffraction pattern are: (d, intensity,index) I1.6, 100,100; 4.36, 50, 210;3.49,40, 2ll;2.877,40, 400;2.433, 60,212. The nameis in honorof Thomasand JosephPeters. Introduction under catalog # NMNH 148973at the Smithsonian Institution. The new mineral describedherein was sent to us for examinationby Mr. ThomasPeters of the Pater- Morphology son Museum,who had obtainedit from Mr. Nicho- Petersiteoccurs as prismatic hexagonalcrystals las Facciolla, who found it in early 1981. Mr. of simplemorphology. The only forms presentare Peters'examination by SEM techniquessuggested the prism {1010}, and the pinacoid {0001}. The a hexagonal morphology for the mineral and our crystals are usually euhedral and occur in radiating subsequentX-ray diffraction study showedit to be clustersand sprayswhich are somewhatisolated on hexagonaland isostructural with members of the the matrix (Fig. -
Gaspéite-Magnesite Solid Solutions and Their Significance
78 Advances in Regolith GASPÉITE-MAGNESITE SOLID SOLUTIONS AND THEIR SIGNIFICANCE Meagan E. Clissold, Peter Leverett & Peter A. Williams School of Science, Food and Horticulture, University of Western Sydney, Locked Bag 1797, Penrith South DC NSW 1797 It is a surprising fact that, despite the increasing number of secondary minerals of Ni(II) recognized from oxidized base metal deposits (Anthony et al. 2003), the supergene chemistry responsible for their formation remains poorly understood. An understanding of this chemistry would be desirable in view of its importance with respect to geochemical exploration for the element, its behaviour in the regolith and the potential development of commercially exploitable secondary nickel resources. Of the secondary nickel minerals known, gaspéite, NiCO3, is perhaps the most common and has been observed in a number of Western Australian deposits. Notable among these is the 132 pit at Widgiemooltha, near Kambalda, WA (Nickel et al.1994). The supergene profile of the 132 pit consists of 5 zones: oxide, carbonate, violarite-pyrite, transition and primary zone. The carbonate zone is 3-12 m below surface and is characterized by the occurrence of a number of flat-lying to sub-horizontal veins of gaspéite that cut across altered wall rock comprising tremolite and goethite. These veins extend from what was a large sulfide body across the matrix layer. Single gaspéite veins have a size of 5 x 5 x 0.05 m on average and may occur in masses of up to 10 x 10 x 1 m; they are typically massive to either granular or fibrous. From the lower part of the carbonate zone upwards there is a progressive decrease in the amount of gaspéite and other carbonate minerals, and their respective nickel contents. -
Violarite Fe2+Ni S4
2+ 3+ Violarite Fe Ni2 S4 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Cubic. Point Group: 4/m 32/m. As nodules up to 0.5 cm and massive. Physical Properties: Cleavage: Perfect on {001}. Tenacity: Brittle. Hardness = 4.5–5.5 VHN = 455–493 (100 g load). D(meas.) = n.d. D(calc.) = 4.79 Optical Properties: Opaque. Color: Violet-gray; distinctly violet in reflected light. Luster: Metallic. R: (400) 39.0, (420) 39.6, (440) 40.2, (460) 40.6, (480) 41.0, (500) 41.4, (520) 41.9, (540) 42.5, (560) 43.1, (580) 43.8, (600) 44.3, (620) 44.8, (640) 45.4, (660) 45.8, (680) 46.2, (700) 46.6 Cell Data: Space Group: Fd3m. a = 9.51 Z = 8 X-ray Powder Pattern: Vermilion mine, Sudbury, Canada. 2.85 (100), 1.674 (80), 1.820 (60), 2.36 (50), 1.059 (50), 1.183 (40), 1.115 (40) Chemistry: (1) (2) (3) Fe 17.01 19.33 18.52 Ni 38.68 33.94 38.94 Co 1.05 2.50 Cu 1.12 1.05 S 41.68 42.17 42.54 insol. 0.40 1.31 Total 99.94 100.30 100.00 (1) Vermilion mine, Sudbury, Canada; contains trace chalcopyrite. (2) Friday mine, Julian, California, USA; contains trace chalcopyrite. (3) FeNi2S4. Mineral Group: Linnaeite group. Occurrence: Of hydrothermal origin, with other sulfides. Association: Pyrrhotite, millerite, chalcopyrite, pentlandite. Distribution: In the USA, from the Friday mine, Julian, San Diego Co., California; the Key West mine, Clark Co., Nevada; the Copper King mine, Gold Hill district, Boulder Co., Colorado; the Lick Fork deposit, Floyd Co., Virginia; and the Gap Nickel mine, Lancaster Co., Pennsylvania. -
Mineraiogy, Lithostratigraphy and Geochemistry of North Lngebright Lake, Saskatchewan, Canada
Mineraiogy, Lithostratigraphy and Geochemistry of North lngebright Lake, Saskatchewan, Canada BY Yuqiang Shang A Thesis Submitted to the Faculty of Graduate Studies in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy Department of Geological Sciences University of Manitoba Winnipeg, Manitoba (c) December, 2000 National Library Bibliothèque nationale 1+1 ,,,da du Canada Acquisitions and Acquisitions et Bibliographic Services seMces bibliographiques 395 Weliington Street 395. rue Wellington OttawaON KlAON4 Oîtawa ON KIA ON4 Canada Canada The author has granted a non- L'auteur a accordé une licence non exclusive licence allowing the exclusive permettant a la National Library of Canada to Bhliotheque nationale du Canada de reproduce, loan, distri'bute or sell reproduire, prêter, distribuer ou copies of this thesis in microform, vendre des copies de cette thèse sous paper or electronic formats. la forme de microfiche/nlm, de reproduction sur papier ou sur format électronique. The author retains ownership of the L'auteur conserve la propriété du copyright in this thesis. Neither the droit d'auteur qui protège cette thèse. thesis nor substantial extracts from it Ni la thèse ni des extraits substantiels may be printed or otherwise de celle-ci ne doivent être imp~imés reproduced without the author's ou autrement reproduits sans son permission. autorisation. THE UNIVERSITY OF MANITOBA FACULTY OF GRADUATE STUDIES ***** COPYRIGHT PERMISSION PAGE MineraIogy, Lithostratigraphy and Geochemistry of North Iigebright Lake, -
Leightonite K2ca2cu(SO4)4 • 2H2O C 2001-2005 Mineral Data Publishing, Version 1
Leightonite K2Ca2Cu(SO4)4 • 2H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Orthorhombic. Point Group: 2/m 2/m 2/m. Lathlike crystals, flattened on {100}, elongated along [010], or equant, showing {100}, {101}, {110}, {113}, several other forms, to 4 mm; commonly forms cross-fiber veinlets. Twinning: On {201}. Physical Properties: Hardness = 3 D(meas.) = 2.95 D(calc.) = 2.95 Optical Properties: Transparent to translucent. Color: Pale watery blue to greenish blue; pale blue in transmitted light. Luster: Vitreous. Optical Class: Biaxial (–). Orientation: X = c; Y = b; Z = a. Dispersion: r> v,moderately strong. α = 1.574–1.578 β = 1.587 γ = 1.595 2V(meas.) = ∼60◦ 2V(calc.) = 89◦060 Cell Data: Space Group: F mmm. a = 11.654(2) b = 7.497(1) c = 10.097(1) β = 125.21(1)◦ Z=2 X-ray Powder Pattern: Chuquicamata, Chile. 2.90 (100), 3.18 (60), 1.781 (30), 2.22 (20), 2.51 (10), 2.40 (10), 1.461 (10) Chemistry: (1) (2) SO3 49.33 49.87 CuO 11.97 12.39 CaO 18.41 17.46 Na2O 0.56 K2O 13.93 14.67 H2O 5.71 5.61 Total 99.91 100.00 • (1) Chuquicamata, Chile; corresponds to (K1.92Na0.12)Σ=2.04Ca2.13Cu0.98(SO4)4.00 2.06H2O. • (2) K2Ca2Cu(SO4)4 2H2O. Occurrence: Of localized occurrence in the oxidized zone of a copper deposit, probably formed under conditions of low acidity (Chuquicamata, Chile). Association: Natrochalcite, bl¨odite, atacamite, bellingerite, kr¨ohnkite,gypsum, quartz (Chuquicamata, Chile); chalcanthite, anhydrite, lammerite (Tsumeb, Namibia). -
Lammerite Cu3(Aso4,PO4)
Lammerite Cu3(AsO4, PO4)2 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. Crystals, to 2 mm, are prismatic along [001] to tabular on {100} and terminated by {011}; additional forms include {010} and striated {120}; in radial spheroidal aggregates. Physical Properties: Cleavage: Perfect on {010}; good on {100}; imperfect on {001}. Hardness = 3.5–4 D(meas.) = 4.9–5.18 D(calc.) = 5.263 Optical Properties: Transparent. Color: Dark green. Streak: Pale green. Luster: Adamantine, vitreous on cleavage surfaces. Optical Class: Biaxial (+). Pleochroism: Strong; X = pale blue; Y = sky-blue; Z = pale bluish green. Orientation: X = b; Z ∧ c ' 40◦. Dispersion: rv, very strong. α = ∼1.89 β = 1.90–2.06 γ = 1.95–2.14 2V(meas.) = 54(5)◦ 2V(calc.) = 50◦ Cell Data: Space Group: P 21/a. a = 5.079(1) b = 11.611(2) c = 5.394(1) β = 111.72(2)◦ Z=2 X-ray Powder Pattern: Laurani, Bolivia. 2.89 (10), 2.52 (9), 3.06 (8), 3.00 (8), 2.62 (8), 2.59 (8), 2.84 (7) Chemistry: (1) (2) As2O5 49.8 32.64 P2O5 12.40 FeO 0.2 0.06 CuO 49.9 54.64 ZnO 0.8 0.11 MgO 0.2 Total 100.9 99.85 1− (1) Laurani, Bolivia; by electron microprobe, absence of (OH) and H2O confirmed by IR; corresponding to (Cu2.90Zn0.05Mg0.02Fe0.01)Σ=2.98(As1.00O4)2. (2) Tolbachik fissure volcano, Russia; by electron microprobe, corresponding to (Cu2.96Zn0.01)Σ=2.97[(As0.62P0.38)Σ=1.00O4]2. -
02-Newsl7tabs 27..32
Mineralogical Magazine, February 2011, Vol. 75(1), pp. 27À31 CNMNC Newsletter IMA Commission on New Minerals, Nomenclature and Classification (CNMNC) NEWSLETTER 7 New minerals and nomenclature modifications approved in 2010 1 2 3 P. A. WILLIAMS (Chairman, CNMNC), F. HATERT (Vice-Chairman, CNMNC), M. PASERO (Vice-Chairman, 4 CNMNC) AND S. J. MILLS (Secretary, CNMNC) 1 School of Natural Sciences, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797, Australia À [email protected] 2 Laboratoire de Mine´ralogie, Universite´ de Lie`ge, B-4000 Lie`ge, Belgium À [email protected] 3 Dipartimento di Scienze della Terra, Universita` degli Studi di Pisa, Via Santa Maria 53, I-56126 Pisa, Italy À [email protected] 4 Department of Earth and Ocean Sciences, University of British Columbia, Vancouver BC, Canada V6T 1Z4 À [email protected] The information given here is provided by the IMA Commission on New Minerals, Nomenclature and Classification for comparative purposes and as a service to mineralogists working on new species. Each mineral is described in the following format: NEW MINERAL PROPOSALS APPROVED IN NOVEMBER 2 010 Mineral name, if the authors agree on its IMA No. 2010-044 release prior to the full description appearing Titanium in press Ti Chemical formula Orebody 31, Luobusa mining district, in Qusong Type locality County, Tibet (29º5’N 92º5’E) Full authorship of proposal Fang Qing-Song, Shi Ni-Cheng, Li Guo-Wu*, E-mail address of corresponding author Bai Wen-Ji, Yang Jing-Sui, Xiong Ming, Rong Relationship to other -
Sulfide Minerals in the G and H Chromitite Zones of the Stillwater Complex, Montana
Sulfide Minerals in the G and H Chromitite Zones of the Stillwater Complex, Montana GEOLOGICAL SURVEY PROFESSIONAL PAPER 694 Sulfide Minerals in the G and H Chromitite Zones of the Stillwater Complex, Montana By NORMAN J PAGE GEOLOGICAL SURVEY PROFESSIONAL PAPER 694 The relationship of the amount, relative abundance, and size of grains of selected sulfide minerals to the crystallization of a basaltic magma UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON: 1971 UNITED STATES DEPARTMENT OF THE INTERIOR ROGERS C. B. MORTON, Secretary GEOLOGICAL SURVEY William T. Pecora, Director Library of CongresR catalog-card No. 70-610589 For sale by the Superintendent of Documents, U.S. Government Printin&' Otrice Washin&'ton, D.C. 20402 - Price 35 cents (paper cover) CONTENTS Page Abstract------------------------------------------------------------------------------------------------------------ 1 Introduction________________________________________________________________________________________________________ 1 Acknowledgments--------------------------------------------------------------------------------------------------- 4 Sulfide occurrences-------------------------------------------------------------------------------------------------- 4 Sulfide inclusions in cumulus minerals_____________________________________________________________________________ 4 Fabrtc______________________________________________________________________________________________________ 5 Phase assemblages__________________________________________________________________________________________ -
From the Lingyan Temple, Changqing, Shandong, China
Technical Study of Polychrome Arhat Figures Dated From the Song Dynasty(960-1279 CE) From the Lingyan Temple, Changqing, Shandong, China Yongdong Tong University of Science and Technology Beijing Youzhen Cai Shandong Cultural Relic Conservation and Restoration Center Xuening Wang Shandong Cultural Relic Conservation and Restoration Center Zhimin Li Shandong University Austin Nevin Courtauld Institute of Art: The Courtauld Institute of Art Qinglin Ma ( [email protected] ) Shandong University https://orcid.org/0000-0002-5542-2388 Research Article Keywords: Lingyan Temple, Arhat statues, paint layers, scientic analysis Posted Date: June 30th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-662279/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/29 Abstract Scientic analysis revealed the materials and techniques used in the process of making the polychrome sculptures providing a solid foundation for the protection and restoration of the painted statues. In addition analysis revealed changes in colour schemes applied to the sculptures can provide the basis for the virtual restoration of the painted statues. In order carry out scientically-informed protection and restoration of the Bodhidharma statue from the Lingyan Temple, Changqinq, Shandong, several analytical methods such as optical microscope (OM), Micro-Raman spectroscopy (μ-RS), scanning electron microscopy coupled with energy dispersive X-ray analysis (SEM-EDS) and Fourier transform infrared spectroscopy (FTIR) were employed. Analysis clearly reveal the information including the stratigraphic structure and the composition of pigment. The use of silver foils and golden yellow pyrophyllite mineral to replace gold foils were found in the gilding paint layer in the later repainting after the Song Dynasty. -
The Paragenesis of Silver Minerals in the Pb-Zn Stan Terg Deposit, Kosovo: an Example of Precious Metal Epithermal Mineralization
2016, vol. 42 (1): 19–29 The paragenesis of silver minerals in the Pb-Zn Stan Terg deposit, Kosovo: an example of precious metal epithermal mineralization Joanna Kołodziejczyk1, Jaroslav Pršek1, Burim Asllani2, Feriz Maliqi3 1 AGH University of Science and Technology, Faculty of Geology, Geophysics and Environmental Protection, Department of Economic Geology; al. A. Mickiewicza 30, 30-059 Krakow, Poland 2 E&E Experts LLC, 10000, Prishtina, Republic of Kosovo 3 Trepça – Enterprise under AKP Administration, Parku Industrial Mitrovicë, Mitrovicë, 40000, Republic of Kosovo © 2016 Authors. This is an open access publication, which can be used, distributed and reproduced in any medium according to the Creative Commons CC-BY 4.0 License requiring that the original work has been properly cited. Received: 9 February 2016; accepted: 12 April 2016 Abstract: This study reports silver mineral association found recently in the Stan Terg lead and zinc mine, locat- ed in the Vardar zone (in northern Kosovo). The described mineralization comprises pyrargyrite (Ag3SbS3), frei- eslebenite (AgPbSbS3), high-Ag bearing tetrahedrite and freibergite ((Ag4+2xCu2−2x)[(Cu,Ag)4(Fe, Zn)2]Σ6Sb4S12S1−x with (0 < x < 1)); as well as native compounds (Electrum, composition of those minerals was confirmed by the electron microprobe. The freibergite from native silver is native antimony). The Ag-minerals occur in vuggs and cracks in a massive galena ore and have signs of the latest minerals, which precipitated in the deposit. The chem- ical of the Stan Terg deposit reveals zonality and contains between 13.91–20.28% of Ag. The high concentration of Ag in solutions is also indicated by relatively high silver content in Au-Ag alloy (electrum), which is between 47.02% and 73.19% of Ag.