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Intergrown Emerald Specimen from Chivor Tity Was Confirmed by Raman Spectroscopy
Editor Nathan Renfro Contributing Editors Elise A. Skalwold and John I. Koivula Intergrown Emerald Specimen from Chivor tity was confirmed by Raman spectroscopy. The inclusion exhibited a well-formed hexagonal prismatic shape with Colombia’s Chivor emerald mines are located in the east- pyramid-like termination (figure 2). Although intergrowth ern zone of the Eastern Cordillera range of the Andes emerald crystals have been described and documented in Mountains. Chivor translates to “green and rich land” in the literature several times (G. Grundmann and G. Giu- Chibcha, the language of the indigenous people who were liani, “Emeralds of the world,” in G. Giuliani et al., Eds., already mining emerald more than 500 years ago, before Emeralds of the World, extraLapis English, No. 2, 2002, pp. the arrival of the Spanish conquistadors (D. Fortaleché et al., “The Colombian emerald industry: Winds of change,” Fall 2017 G&G, pp. 332–358). Chivor emeralds exhibit a bright green color with a tint of blue; they have relatively Figure 1. An emerald crystal inclusion measuring high clarity and fewer inclusions than emeralds found in ~2.67 × 2.71 × 5.43 mm is found inside this large Colombia’s western belt. emerald specimen (18.35 × 10.69 × 9.79 mm) from Colombia’s Chivor mine. Photo by John Jairo Zamora. The authors recently examined a rough emerald crystal specimen (figure 1), measuring 18.35 × 10.69 × 9.79 mm, reportedly from Chivor. This crystal weighed 3.22 g (16.10 ct) and had a prismatic hexagonal crystal shape. Standard gemological examination confirmed the gemstone to be emerald, and ultraviolet/visible/near-infrared (UV-Vis-NIR) spectroscopy showed a classic Colombian emerald absorp- tion spectrum. -
New Mineral Names*
American Mineralogist, Volume 68, pages 280-2E3, 1983 NEW MINERAL NAMES* MrcnnBr- FrelscHen AND ADoLF Pnnsr Arsendescloizite* The mineral occurs at Uchucchacua,Peru, in acicular crystals up to 2fi) x 20 microns, associatedwith galena, manganoan (1982) Paul Keller and P. J. Dunn Arsendescloizite, a new sphalerite, pyrite, pyrrhotite, and alabandite, with gangue of mineral from Tsumeb. Mineralog. Record, 13, 155-157. quartz, bustamite, rhodonite, and calcite. Also found at Stitra, pyrite-pyrrhotite in rhyo- Microprobe analysis (HzO by TGA) gave AszOs 26.5, PbO Sweden,in a metamorphosed deposit 52.3,ZnO1E.5, FeO 0.3, Il2O2.9, sum 100.5%,corresponding to litic and dacitic rocks; in roundedgrains up to 50 fl.min diameter, associated with galena, freibergite, gudmundite, manganoan Pb1.s6(Zn1.63Fe6.oJ(AsOaXOH)1a or PbZn(AsO+XOH), the ar- senateanalogue ofdescloizite. The mineral is slightly soluble in sphalerite,bismuth, and spessartine. hot HNO3. The name is for A. Benavides, for his contribution to the Weissenbergand precessionmeasurements show the mineral development of mining in Peru. Type material is at the Ecole (Uchucchacua)and at the Free to be orthorhombic, space group F212121,a : 6.075, b = 9.358, Natl. Superieuredes Mines, Paris (SAtra). c = 7.$44, Z = 4, D. calc. 6.57. The strongestX-ray lines University, Amsterdam, Netherlands M.F. (31 eiven) are 4.23(6)(lll); 3.23(lOXl02);2.88(10)(210,031); 2.60 Kolfanite* (E)(13 I ) ; 2.W6)Q3r) ; I .65(6X33I, 143,233); r.559 (EX3I 3,060,25I ). Crystalsare tabular up to 1.0 x 0.4 x 0.5 mm in size, on {001}, A. -
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 -
List of New Mineral Names: with an Index of Authors
415 A (fifth) list of new mineral names: with an index of authors. 1 By L. J. S~v.scs~, M.A., F.G.S. Assistant in the ~Iineral Department of the,Brltish Museum. [Communicated June 7, 1910.] Aglaurito. R. Handmann, 1907. Zeita. Min. Geol. Stuttgart, col. i, p. 78. Orthoc]ase-felspar with a fine blue reflection forming a constituent of quartz-porphyry (Aglauritporphyr) from Teplitz, Bohemia. Named from ~,Xavpo~ ---- ~Xa&, bright. Alaito. K. A. ~Yenadkevi~, 1909. BuU. Acad. Sci. Saint-P6tersbourg, ser. 6, col. iii, p. 185 (A~am~s). Hydrate~l vanadic oxide, V205. H~O, forming blood=red, mossy growths with silky lustre. Founi] with turanite (q. v.) in thct neighbourhood of the Alai Mountains, Russian Central Asia. Alamosite. C. Palaehe and H. E. Merwin, 1909. Amer. Journ. Sci., ser. 4, col. xxvii, p. 899; Zeits. Kryst. Min., col. xlvi, p. 518. Lead recta-silicate, PbSiOs, occurring as snow-white, radially fibrous masses. Crystals are monoclinic, though apparently not isom0rphous with wol]astonite. From Alamos, Sonora, Mexico. Prepared artificially by S. Hilpert and P. Weiller, Ber. Deutsch. Chem. Ges., 1909, col. xlii, p. 2969. Aloisiite. L. Colomba, 1908. Rend. B. Accad. Lincei, Roma, set. 5, col. xvii, sere. 2, p. 233. A hydrated sub-silicate of calcium, ferrous iron, magnesium, sodium, and hydrogen, (R pp, R',), SiO,, occurring in an amorphous condition, intimately mixed with oalcinm carbonate, in a palagonite-tuff at Fort Portal, Uganda. Named in honour of H.R.H. Prince Luigi Amedeo of Savoy, Duke of Abruzzi. Aloisius or Aloysius is a Latin form of Luigi or I~ewis. -
Structure of Synthetic Liimg,Cu)Cuz[Siz06]Z: a Unique Chain Silicate Related to Pyroxene
American Mineralogist, Volume 82, pages 143-148, 1997 Structure of synthetic LiiMg,Cu)Cuz[Siz06]z: A unique chain silicate related to pyroxene HIROYUKI HORIUCHI,1 AKIHIRO SAITO,I TOSHINAGA TACHI,2 AND HIROSHI NAGASAWA2 'Mineralogical Institute, Faculty of Science, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113, Japan 'Department of Chemistry, Faculty of Science, Gakushuin University, 1-5-1 Mejiro, Toshima-ku, Tokyo 171, Japan ABSTRACT A unique Cu-bearing chain silicate, Li2(Mg,Cu)Cuz[Si206b was synthesized, and the structure was determined by single-cry~tal X-ray diffraction techniques. The structure was found to be triclinic, spacoe group PI, with unit-cell parameters a = 5.7068(7), b = 7.4784(9), c = 5.2193(3) A, ex = 99.911(8), J3 = 97.436(8), 'Y = 84.52(1)°, and Z = 1. The arrangement of zweier single chains, [Siz06], differs significantly from chain arrange- ments in the pyroxene and pyroxenoid structures, and the "I-beam" description of the pyroxene structure is not applicable. The structure may be classified as a new derivative type of the pyroxene structure, with an "oblique I-beam". Cu atoms are coordinated by four atoms in a square-planar arrangement with 1.94-2.00 A for Cu-O and two atoms with °longer Cu-O distances of 2.41-2.92 A, consistent with the crystal-field stabilization° ~f the d9. electroni~ structure of Cu2+. The square-planar Cu04 units form a [CunOZn+2] nbbon with n = 3 ill the structure, which is also found in Cu-bearing chain silicates such as shattuckite and plancheite with n > 3. -
Mottramite Pbcu(VO4)(OH) C 2001-2005 Mineral Data Publishing, Version 1 Crystal Data: Orthorhombic
Mottramite PbCu(VO4)(OH) c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Orthorhombic. Point Group: 2/m 2/m 2/m. As crystals, equant or dipyramidal {111}, prismatic [001] or [100], with {101}, {201}, many others, to 3 mm, in drusy crusts, botryoidal, usually granular to compact, massive. Physical Properties: Fracture: Small conchoidal to uneven. Tenacity: Brittle. Hardness = 3–3.5 D(meas.) = ∼5.9 D(calc.) = 6.187 Optical Properties: Transparent to nearly opaque. Color: Grass-green, olive-green, yellow- green, siskin-green, blackish brown, nearly black. Streak: Yellowish green. Luster: Greasy. Optical Class: Biaxial (–), rarely biaxial (+). Pleochroism: Weak to strong; X = Y = canary-yellow to greenish yellow; Z = brownish yellow. Orientation: X = c; Y = b; Z = a. Dispersion: r> v,strong; rarely r< v.α= 2.17(2) β = 2.26(2) γ = 2.32(2) 2V(meas.) = ∼73◦ Cell Data: Space Group: P nma. a = 7.667–7.730 b = 6.034–6.067 c = 9.278–9.332 Z=4 X-ray Powder Pattern: Mottram St. Andrew, England; close to descloizite. 3.24 (vvs), 5.07 (vs), 2.87 (vs), 2.68 (vs), 2.66 (vs), 2.59 (vs), 1.648 (vs) Chemistry: (1) (2) (1) (2) CrO3 0.50 ZnO 0.31 10.08 P2O5 0.24 PbO 55.64 55.30 As2O5 1.33 H2O 3.57 2.23 V2O5 21.21 22.53 insol. 0.17 CuO 17.05 9.86 Total 100.02 100.00 (1) Bisbee, Arizona, USA; average of three analyses. (2) Pb(Cu, Zn)(VO4)(OH) with Zn:Cu = 1:1. -
Formation of Chrysocolla and Secondary Copper Phosphates in the Highly Weathered Supergene Zones of Some Australian Deposits
Records of the Australian Museum (2001) Vol. 53: 49–56. ISSN 0067-1975 Formation of Chrysocolla and Secondary Copper Phosphates in the Highly Weathered Supergene Zones of Some Australian Deposits MARTIN J. CRANE, JAMES L. SHARPE AND PETER A. WILLIAMS School of Science, University of Western Sydney, Locked Bag 1797, Penrith South DC NSW 1797, Australia [email protected] (corresponding author) ABSTRACT. Intense weathering of copper orebodies in New South Wales and Queensland, Australia has produced an unusual suite of secondary copper minerals comprising chrysocolla, azurite, malachite and the phosphates libethenite and pseudomalachite. The phosphates persist in outcrop and show a marked zoning with libethenite confined to near-surface areas. Abundant chrysocolla is also found in these environments, but never replaces the two secondary phosphates or azurite. This leads to unusual assemblages of secondary copper minerals, that can, however, be explained by equilibrium models. Data from the literature are used to develop a comprehensive geochemical model that describes for the first time the origin and geochemical setting of this style of economically important mineralization. CRANE, MARTIN J., JAMES L. SHARPE & PETER A. WILLIAMS, 2001. Formation of chrysocolla and secondary copper phosphates in the highly weathered supergene zones of some Australian deposits. Records of the Australian Museum 53(1): 49–56. Recent exploitation of oxide copper resources in Australia these deposits are characterized by an abundance of the has enabled us to examine supergene mineral distributions secondary copper phosphates libethenite and pseudo- in several orebodies that have been subjected to intense malachite associated with smaller amounts of cornetite and weathering. -
Namibia Critical Metals Inc
Namibia Critical Metals Inc. (formerly Namibia Rare Earths Inc.) CONSOLIDATED FINANCIAL STATEMENTS FOR THE YEARS ENDED NOVEMBER 30, 2018 AND 2017 NAMIBIA CRITICAL METALS INC. – CONSOLIDATED FINANCIAL STATEMENTS NAMIBIA CRITICAL METALS INC. MANAGEMENT’S DISCUSSION AND ANALYSIS This management's discussion and analysis of the financial condition and results of operations ("MD&A") of Namibia Critical Metals Inc. (the “Company” formerly known as Namibia Rare Earths Inc.) is dated March 25, 2019 and provides an analysis of the Company’s financial results and progress for the years ended November 2018 and 2017. This MD&A should be read in conjunction with the Company's audited consolidated financial statements for the years ended November 30, 2018 and 2017 and related notes thereto, which were prepared in accordance with International Financial Reporting Standards (“IFRS”) as issued by the International Accounting Standards Board (“IASB”) and Interpretations of the IFRS Interpretations Committee (“IFRIC”). All amounts are expressed in Canadian dollars unless otherwise noted. This discussion includes certain statements that may be deemed “forward-looking statements”. All statements in this discussion, other than statements of historical fact, that address exploration drilling, exploitation activities and events or developments that the Company expects, are forward-looking statements. Although the Company believes the expectations expressed in such forward-looking statements are based on reasonable assumptions, such statements are not guarantees of future performance and actual results or developments may differ materially from those in the forward-looking statements. Factors that could cause actual results to differ materially from those in forward-looking statements include market prices, exploitation and exploration results, continued availability of capital and financing and general economic, market or business conditions. -
B Clifford Frondel
CATALOGUE OF. MINERAL PSEUDOMORPHS IN THE AMERICAN MUSEUM -B CLIFFORD FRONDEL BU.LLETIN OF THEAMRICANMUSEUM' OF NA.TURAL HISTORY. VOLUME LXVII, 1935- -ARTIC-LE IX- NEW YORK Tebruary 26, 1935 4 2 <~~~~~~~~~~~~~7 - A~~~~~~~~~~~~~~~, 4~~~~~~~~~~~~~~~~~~~~~~~~~~~~~4 4 4 A .~~~~~~~~~~~~~~~~~~~~~~~~~~4- -> " -~~~~~~~~~4~~. v-~~~~~~~~~~~~~~~~~~t V-~ ~~~~~~~~~~~~~~~~ 'W. - /7~~~~~~~~~~~~~~~~~~~~~~~~~~7 7-r ~~~~~~~~~-A~~~~ ~ ~ ~ ~ ~ ~ ~ ~ ~ -'c~ ~ ~ ' -7L~ ~ ~ ~ ~ 7 54.9:07 (74.71) Article IX.-CATALOGUE OF MINERAL PSEUDOMORPHS IN THE AMERICAN MUSEUM OF NATURAL HISTORY' BY CLIFFORD FRONDEL CONTENTS PAGE INTRODUCTION .................. 389 Definition.389 Literature.390 New Pseudomorphse .393 METHOD OF DESCRIPTION.393 ORIGIN OF SUBSTITUTION AND INCRUSTATION PSEUDOMORPHS.396 Colloidal Origin: Adsorption and Peptization.396 Conditions Controlling Peptization.401 Volume Relations.403 DESCRIPTION OF SPECIMENS.403 INTRODUCTION DEFINITION.-A pseudomorph is defined as a mineral which has the outward form proper to another species of mineral whose place it has taken through the action of some agency.2 This precise use of the term excludes the regular cavities left by the removal of a crystal from its matrix (molds), since these are voids and not solids,3 and would also exclude those cases in which organic material has been replaced by quartz or some other mineral because the original substance is here not a mineral. The general usage of the term is to include as pseudomorphs both petrifactions and molds, and also: (1) Any mineral change in which the outlines of the original mineral are preserved, whether this surface be a euhedral crystal form or the irregular bounding surface of an embedded grain or of an aggregate. (2) Any mineral change which has been accomplished without change of volume, as evidenced by the undistorted preservation of an original texture or structure, whether this be the equal volume replacement of a single crystal or of a rock mass on a geologic scale. -
The Mineral Industry of Namibia in 1997
THE MINERAL INDUSTRY OF NAMIBIA By George J. Coakley Namibia is located on the southwest coast of Africa between The system of taxation on diamond mining consisted of three South Africa and Angola. The 825,418 square kilometer country separate taxes: income, diamond profits, and diamond export had an estimated population in 1997 of 1.63 million and a gross duties. The latter has now been replaced by a 10% royalty. The domestic product (GDP) per capita of about $2,070. The mineral overall income tax on diamond mining companies is levied at the industry of Namibia provided about 15% of the country’s $3.2 rate of 55% of taxable income, plus a surcharge of 10% on the billion1 GDP in 1996 (iafrica.com Namibia, [no date] General market value of diamonds shipped and sold. The Income Tax Act information—GDP figures: accessed October 1, 1998 at URL provides that this 10% surcharge paid as diamond profits tax be http://trade.iafrica.com.na/generalinfo/factsfigures/ credited against the income tax payable by diamond mines. A composition.htm) and annually contributes to approximately 50% new Diamond Act is expected to be promulgated in 1998. of the value of total exports earnings. In 1997, the industry was The fiscal regime for oil exploration companies consists of dominated by three established mining companies—Namdeb three principal elements: an income tax and an Additional Profits Diamond Corp (Pty.) Ltd., Rossing Uranium Ltd., and Tsumeb Tax (APT), both levied in terms of the Petroleum (Taxation) Act, Corp. Ltd. The Government’s proactive policies encouraged new No. -
Minerals Found in Michigan Listed by County
Michigan Minerals Listed by Mineral Name Based on MI DEQ GSD Bulletin 6 “Mineralogy of Michigan” Actinolite, Dickinson, Gogebic, Gratiot, and Anthonyite, Houghton County Marquette counties Anthophyllite, Dickinson, and Marquette counties Aegirinaugite, Marquette County Antigorite, Dickinson, and Marquette counties Aegirine, Marquette County Apatite, Baraga, Dickinson, Houghton, Iron, Albite, Dickinson, Gratiot, Houghton, Keweenaw, Kalkaska, Keweenaw, Marquette, and Monroe and Marquette counties counties Algodonite, Baraga, Houghton, Keweenaw, and Aphrosiderite, Gogebic, Iron, and Marquette Ontonagon counties counties Allanite, Gogebic, Iron, and Marquette counties Apophyllite, Houghton, and Keweenaw counties Almandite, Dickinson, Keweenaw, and Marquette Aragonite, Gogebic, Iron, Jackson, Marquette, and counties Monroe counties Alunite, Iron County Arsenopyrite, Marquette, and Menominee counties Analcite, Houghton, Keweenaw, and Ontonagon counties Atacamite, Houghton, Keweenaw, and Ontonagon counties Anatase, Gratiot, Houghton, Keweenaw, Marquette, and Ontonagon counties Augite, Dickinson, Genesee, Gratiot, Houghton, Iron, Keweenaw, Marquette, and Ontonagon counties Andalusite, Iron, and Marquette counties Awarurite, Marquette County Andesine, Keweenaw County Axinite, Gogebic, and Marquette counties Andradite, Dickinson County Azurite, Dickinson, Keweenaw, Marquette, and Anglesite, Marquette County Ontonagon counties Anhydrite, Bay, Berrien, Gratiot, Houghton, Babingtonite, Keweenaw County Isabella, Kalamazoo, Kent, Keweenaw, Macomb, Manistee, -
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682 NOTES AND NEWS atoms are less restricted and their vibrations parallel to the c axis are bigger than those in the (001) plane. Sasset al. (1957) reports a rms dis- placementfor oxygenin CaCOeof about 0.09 A parallel to c which is in good agreement with the value reported in this investigation. Their two anisotropic displacementsin the (001) plane,0.06 A and 0'11 A, re- spectively parallel and perpendicular to the a axis, bracket the value of 0.086 A of Table 2. AcrNowr-npGMENTS The writers wish to expresstheir appreciationto Dr. A. S. Ginzbarg and Miss E. E. Allen who wrote the programsfor the three-dimensional Fourier and least-squarescomputations and to Dr' R. A. Rowland for his critical reading of the manuscript. Rrrnnnmcrs Bnlorev,W. F.,Bunsr, J. l-., eNnGnm, D. L (1953),Crystal Chemistry and Difierential Thermal Efiects of Dolomite: Amer. Mineral.,38,207. Snss, R. L., Vmar.n, R., ero DoNonun, J. (1957), Interatomic Distances and Thermal Anisotropy in Sodium Nitrate and Calcite: Acta Cryst., l0' 567. Wvcrorr, W. G., aNo MnnwtN, H.E. (1924), The Crystal Structure of Dolomite: Amer' J. Sci.,8, M7 . THE AMERICAN MINERALOGIST, VOL. 44, MAY JUNE, 1959 OCCURRENCEOF JORDANITEIN THE OTAVI MOUNTAINS, SOUTHWEST AFRICA N. L. MenrHAM, Grootfontein,Soulh West Afri'ca An interesting occurrence of jordanite (PbrnAszSz+?)has recently been found at Kupferberg in the Otavi Mountains of South West Africa. The following brief note describesits mode of occurrence and chemical composition. The Kupferberg copper prospect lies in the Otavi Valley about 40 miles South West of Grootfontein.