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Distribution of As, Ni and Co in Tailings and Surface Waters in the Cobalt Area, Ontario1
DISTRIBUTION OF AS, NI AND CO IN TAILINGS AND SURFACE 1 WATERS IN THE COBALT AREA, ONTARIO Jeanne B. Percival2, Y.T. John Kwong3, Charles G. Dumaresq4, Frederick A. Michel5 Abstract: From 1904 until the mid 1930’s and intermittently until 1989, over 450 million troy ounces of silver was mined from the Cobalt area, Ontario. Currently there is no active mining of silver, but the area has seen recent exploration activities for other commodities such as diamonds. Cobalt, however, has not only a renowned mining history, but also an environmental legacy. The area is characterized by remnant historic mine workings and numerous waste rock piles and tailings ponds. Several elements of concern including arsenic, nickel and cobalt continually enter the local watershed from the tailings and waste rock piles. These elements are transported through surface waters to the wetlands in the Farr Creek drainage basin and ultimately enter Lake Timiskaming. Tailings samples are composed of abundant plagioclase with subordinate quartz, chlorite, calcite and dolomite. Less common are K-feldspar, amphibole and mica as well as trace minerals such as erythrite, scorodite and pharmocolite. When efflorescent mineral crusts form on tailings surfaces they are dominated by either gypsum or thenardite. The tailings may contain up to 3.5 wt % Co and 2.2 wt% Ni. Lake sediment and tailings cores show concentrations up to 1.8 wt% As, 0.62 wt% Co and 0.27 wt% Ni in the solids, and 160 mg/L As, 74 mg/L Co and 42 mg/L Ni in the pore waters. One core collected from the infilled Hebert Pond situated within the Nipissing Low Grade Mill tailings impoundment show pore water concentrations in excess of 1,500 mg/L As associated with an organic- rich layer. -
Villyaellenite (Mn, Ca)Mn2(Aso3oh)2(Aso4)2(H2O)4
Villyaellenite (Mn, Ca)Mn2(AsO3OH)2(AsO4)2(H2O)4 Crystal Data: Monoclinic. Point Group: 2/m. Crystals tabular on {100}, to prismatic along [001], showing {100}, {110}, {011}, {010}, {101}, and {001}, to 4 cm; in rosettes and radial aggregates. Physical Properties: Cleavage: Good on {100}. Hardness = ∼4 D(meas.) = 3.20-3.69 D(calc.) = 3.339 Optical Properties: Transparent. Color: Pale rose-red, orange-pink, colorless; colorless in transmitted light. Streak: White. Luster: Vitreous. Optical Class: Biaxial (-). Pleochroism: Moderate; X = very pale orange-pink; Y = exceedingly pale orange-pink; Z = pale orange-pink. Orientation: X = b; Y ∧ c = 30°-40°. Absorption: Z >> X > Y. α = 1.660-1.713 β = 1.670-1.723 γ = 1.676-1.729 2V(meas.) = 70.5°-76° 2V(calc.) = 75°-75.6° Cell Data: Space Group: C2/c. a = 18.400(2) b = 9.4778(10) c = 9.9594(12) β = 96.587(3)° Z = 4 X-ray Powder Pattern: Sainte-Marie-aux-Mines, France. 3.297 (100), 8.476 (90), 3.132 (60), 4.606 (50), 4.761 (40), 3.811 (40), 3.025 (40) Chemistry: (1) (2) As2O5 52.99 50.6 FeO 0.1 MnO 22.40 36.2 ZnO 2.9 CaO 13.58 0.5 H2O 11.42 9.9 Total 100.39 100.2 (1) Sainte-Marie-aux-Mines, France; by electron microprobe, total Mn as MnO, H2O by TGA; 2+ reducing H2O to 10.7% by analogy to other group members, corresponds to (Mn 2.74Ca2.10)Σ=4.84 (H2O)4(AsO3OH)2.31(AsO4)1.69. -
Polarized Infrared Reflectance Spectra of Brushite
Polarized infrared reflectance spectra of brushite (CaHPO4 center dot 2H(2)O) crystal investigation of the phosphate stretching modes Jean-Yves Mevellec, Sophie Quillard, Philippe Deniard, Omar Mekmene, Frederic Gaucheron, Jean-Michel Bouler, Jean-Pierre Buisson To cite this version: Jean-Yves Mevellec, Sophie Quillard, Philippe Deniard, Omar Mekmene, Frederic Gaucheron, et al.. Polarized infrared reflectance spectra of brushite (CaHPO4 center dot 2H(2)O) crystal investigation of the phosphate stretching modes. Spectrochimica Acta Part A: Molecular and Biomolecular Spec- troscopy, Elsevier, 2013, 111, pp.7. 10.1016/j.saa.2013.03.047. hal-00980658 HAL Id: hal-00980658 https://hal.archives-ouvertes.fr/hal-00980658 Submitted on 29 May 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 111 (2013) 7–13 Contents lists available at SciVerse ScienceDirect Spectr ochimica Acta Part A: Molecul ar and Biomo lecular Spectrosco py journal homepage: www.elsevier.com/locate/saa Polarized infrared reflectance spectra of brushite (CaHPO4Á2H2O) crystal investigation of the phosphate stretching modes ⇑ Jean-Yves Mevellec a, , Sophie Quillard b, Philippe Deniard a, Omar Mekmene c, Frédéric Gaucheron c, Jean-Michel Bouler b, Jean-Pierre Buisson a a CNRS, Institut des Matériaux Jean-Rouxel (IMN) – UMR 6502, Université de Nantes, 2 rue de la Houssinière, B.P. -
Geologica Macedonica
UDC 55 In print: ISSN 0352–1206 CODEN – GEOME 2 On line: ISSN 1857–8586 GEOLOGICA MACEDONICA Geologica Macedonica Vol. No pp. Štip 2 91–176 2018 Geologica Macedonica Год. 32 Број стр. Штип Geologica Macedonica Vol. No pp. Štip 2 91–176 2018 Geologica Macedonica Год. 32 Број стр. Штип GEOLOGICA MACEDONICA Published by: – Издава: "Goce Delčev" University in Štip, Faculty of Natural and Technical Sciences, Štip, Republic of Macedonia Универзитет „Гоце Делчев“ во Штип, Факултет за природни и технички науки, Штип, Република Македонија EDITORIAL BOARD Todor Serafimovski (R. Macedonia, Editor in Chief), Blažo Boev (R. Macedonia, Editor), David Alderton (UK), Tadej Dolenec (R. Slovenia), Ivan Zagorchev (R. Bulgaria), Wolfgang Todt (Germany), Nikolay S. Bortnikov (Russia), Clark Burchfiel (USA), Thierry Augé (France), Todor Delipetrov (R. Macedonia), Vlado Bermanec (Croatia), Milorad Jovanovski (R. Macedonia), Spomenko Mihajlović (Serbia), Dragan Milovanović (Serbia), Dejan Prelević (Germany), Albrecht von Quadt (Switzerland) УРЕДУВАЧКИ ОДБОР Тодор Серафимовски (Р. Македонија, главен уредник), Блажо Боев (Р. Македонија, уредник), Дејвид Олдертон (В. Британија), Тадеј Доленец (Р. Словенија), Иван Загорчев (Р. Бугарија), Волфганг Тод (Германија), акад. Николај С. Бортников (Русија), Кларк Барчфил (САД), Тиери Оже (Франција), Тодор Делипетров (Р. Македонија), Владо Берманец (Хрватска), Милорад Јовановски (Р. Македонија), Споменко Михајловиќ (Србија), Драган Миловановиќ (Србија), Дејан Прелевиќ (Германија), Албрехт фон Квад (Швајцарија) Language editor Лектура Marijana Kroteva Маријана Кротева (English) (англиски) Georgi Georgievski Георги Георгиевски (Macedonian) (македонски) Technical editor Технички уредник Blagoja Bogatinoski Благоја Богатиноски Proof-reader Коректор Alena Georgievska Алена Георгиевска Address Адреса GEOLOGICA MACEDONICA GEOLOGICA MACEDONICA EDITORIAL BOARD РЕДАКЦИЈА Faculty of Natural and Technical Sciences Факултет за природни и технички науки P. -
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338 Geologica Macedonica, Vol. 32, No. 2, pp. 95–117 (2018) GEOME 2 IISSN 0352 – 1206 Manuscript received: August 5, 2018 e-ISSN 1857 – 8586 Accepted: November 7, 2018 UDC: 553.46:550.43.08]:504(497.721) 553.497:550.43.08]:504(497.721) Original scientific paper SUPERGENE MINERALOGY OF THE LOJANE Sb-As-Cr DEPOSIT, REPUBLIC OF MACEDONIA: TRACING THE MOBILIZATION OF TOXIC METALS Uwe Kolitsch1,2, Tamara Đorđević2, Goran Tasev3, Todor Serafimovski3, Ivan Boev3, Blažo Boev3 1Mineralogisch-Petrographische Abt., Naturhistorisches Museum, Burgring 7, A-1010 Wien, Austria 2Institut für Mineralogie und Kristallographie, Universität Wien, Althanstr. 14, A-1090 Wien, Austria 3Department of Mineral Deposits, Faculty of Natural and Technical Sciences, “Goce Delčev” University in Štip, Blvd. Goce Delčev 89, 2000 Štip, Republic of Macedonia [email protected] A b s t r a c t: As part of a larger project on the environmental mineralogy and geochemistry of the Lojane Sb- As-Cr deposit, Republic of Macedonia, which was mined for chromite and, later, stibnite until 1979 and is a substantial source of arsenic and antimony pollution, the supergene mineralogy of the deposit was studied. Samples collected on ore and waste dumps were used to identify and characterize the previously uninvestigated suite of supergene mineral phases by standard mineralogical techniques. The following species were determined (in alphabetical order): annaber- gite, arseniosiderite(?), gypsum, hexahydrite, hörnesite, pararealgar, roméite-group minerals, rozenite, scorodite, sen- armontite, stibiconite, sulphur, tripuhyite and valentinite. Their occurrences are described and their local conditions of formation are discussed. High-resolution Raman spectra of hörnesite, hexahydrite and rozenite are provided and com- pared with literature data. -
6H2O, a New Mineral and a Possible Sink for Sb During
1 Revision #1 2 Smamite, Ca2Sb(OH)4[H(AsO4)2]·6H2O, a new mineral and a possible sink for Sb during 3 weathering of fahlore 4 1§ 2 3 4 5 JAKUB PLÁŠIL , ANTHONY R. KAMPF , NICOLAS MEISSER , CÉDRIC LHEUR , THIERRY 5 6 6 BRUNSPERGER AND RADEK ŠKODA 7 8 1 Institute of Physics ASCR, v.v.i., Na Slovance 1999/2, 18221 Prague 8, Czech Republic 9 2 Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 Exposition 10 Boulevard, Los Angeles, CA 90007, USA 11 3 Musée cantonal de géologie, Université de Lausanne, Anthropole, Dorigny, CH-1015 12 Lausanne, Switzerland 13 4 1 rue du St. Laurent, 54280 Seichamps, France 14 5 22 route de Wintzenheim, 68000 Colmar, France 15 6 Department of Geological Sciences, Faculty of Science, Masaryk University, Kotlářská 2, 611 16 37, Brno, Czech Republic 17 18 ABSTRACT 19 Smamite, Ca2Sb(OH)4[H(AsO4)2]·6H2O, is a new mineral species from the Giftgrube mine, 20 Rauenthal, Sainte-Marie-Aux-Mines ore-district, Haut-Rhin department, France. It is a supergene 21 mineral found in quartz-carbonate gangue with disseminated to massive tennantite-tetrahedrite 22 series minerals, native arsenic, Ni-Co arsenides and supergene minerals picropharmacolite, 23 fluckite and pharmacolite. Smamite occurs as lenticular crystals growing in aggregates up to 0.5 24 mm across. The new mineral is whitish to colorless, transparent with vitreous luster and white 25 streak; non-fluorescent under UV radiation. The Mohs hardness is ~3½ ; the tenacity is brittle, 26 the fracture is curved, and there is no apparent cleavage. -
New Mineral Names*
American Mineralogist, Volume 62, pages 1259-1262, 1977 NewMineral Names* MtcHe.rr-Flrlscsnn, Lours J. CesRrAND ADoLF Pe.ssr Franzinite* Six microprobe analyses gave (range and av.): AsrOu 44.96-45.68,45.36; CuO 16.84-20.22,18.81; ZnO 16.78-18.57, Stefano Merlino and Paolo Orlandi (1977)Franzinite, a new min- 17.90;CdO l3 58-14.93,14.08; CaO 0.41-l.ll' 0.80; PbO 0.14- eral phase from Pitigliano,ltaly. Neues Jahrb. Mineral. Mon- 1.42,0.63: MnO 0.'79-1.27,1.07; sum 97 8l-99 54' 98.65 percent, atsh., 163-167. corresponding to (Cu,Zn,Cd).(AsOa), with Cu:Zn:Cd : 1.19: Microchemical analysis gave SiO, 32.44, Al2Os 25.21, Fe"O" Lll:0.55. The mineral is readily dissolvedby concentratedacids 0.04,MgO 0.14,CaO 12.08,Na,O 11.50,K,O 4.24,SOa 10.65, CO, X-ray study showsthe mineral to be monoclinic,space group 12' 154, Cl 036,H,O 1.88,sum 100.08- (O:Cl,) 0.08 : 100.00 Im. or 12/m, a ll.65, b 12.68,c 6.87(all + 0.01A)' B 98 95 + 0.05'' percent. "SiO, and AlrO, were determined by X-ray fluorescence, Z = 6, G calc 4.95 The strongest X-ray lines (46 given) are 6.41 (vvs) account being taken of the proper correction factor for S and Cl (MS) (020, l0T), 3.29 (vSXll2), 2.876 (vSX400), 2.79s and assuming that the weight percentages sum up to 100 0." (222, 321, 240), 1.644(MS). -
Crystal Growth & Design 2007 Vol. 7, No. 12 2756–2763
CRYSTAL GROWTH · Oriented Overgrowth of Pharmacolite (CaHAsO4 2H2O) on & DESIGN Gypsum (CaSO · 2H O) 4 2 2007 Juan Diego Rodríguez-Blanco, Amalia Jiménez,* and Manuel Prieto VOL. 7, NO. 12 Departamento de Geología, UniVersidad de OViedo, Jesús Arias de Velasco s/n, 33005 OViedo, Spain 2756–2763 ReceiVed March 7, 2007; ReVised Manuscript ReceiVed August 31, 2007 ABSTRACT: At neutral pH and 25 °C, the interaction of arsenate-bearing aqueous solutions with gypsum results in surface precipitation of pharmacolite (CaHAsO4 · 2H2O) crystals. The crystals grow oriented onto the gypsum surface, forming an epitaxy. Using an A-centered unit-cell setting for both pharmacolite (Aa) and gypsum (A2/a), the epitaxial relationship is found to be (010)Gy j | (010)Ph and [101]Gy | [101]Ph. Pharmacolite forms thick three-dimensional crystals elongated on [101] with {010}, {111}, and {11j1}j as major forms. Both the crystal morphology and the epitaxial orientation are interpreted on the basis of the bond arrangement in the structure of both phases. The reaction can be envisaged as a sort of solvent-mediated replacement of gypsum by pharmacolite. Under these experimental conditions, the process stops at a “pseudo-equilibrium” end point in which the reactive solids become completely isolated from the aqueous solution by the epitaxial coating of pharmacolite crystals. The thermodynamic solubility product of pharmacolite was determined at this stage and found to be pK ) 4.68 ( 0.04. The reaction paths actually followed by the system and the “true equilibrium” end point are modeled using the geochemical code PHREEQC. Introduction of gypsum and calcium arsenates, detecting that gypsum may contain some arsenic and calcium arsenates may contain some Cocrystallization from aqueous solutions has been receiving sulfur. -
MINERALS with a FRENCH CONNECTION François Fontan and Robert F
MINERALS with a FRENCH CONNECTION François Fontan and Robert F. Martin The Canadian Mineralogist Special Publication 13 TABLE OF CONTENTS Préface vii Preface viii Introduction 1 The scope and contents of this book 1 Early discoveries 1 The three museums in Paris 2 Previous surveys of minerals discovered in France 5 The profile of mineralogy in France today 6 The information to be reported in each entry 6 Bibliography 7 Acknowledgements: special mentions 8 Acknowledgements prepared by François Fontan (2005–2007) 9 Acknowledgements prepared by Robert F. Martin (2007–2017) 9 Hold the presses: new arrivals! 11 Minerals with a type locality in France 13 Minerals discovered elsewhere and named after French citizens 267 Six irregular cases 525 Appendices and indexes 539 The appendices 540 Appendix 1. Minerals with a type locality in France, including New Caledonia: alphabetical listing 541 Appendix 2. Minerals (n = 127) with a type locality in France, including New Caledonia: chronological listing 544 Figure A1. Geographic distribution of mineral discoveries in France 545 Figure A2. Geographic distribution of mineral discoveries in New Caledonia 546 Figure A3. The number of type localities of minerals, grouped by decade 546 Appendix 3. Minerals with a type locality in France, including New Caledonia: geographic distribution 547 Appendix 4. Minerals discovered elsewhere than in France and named after French citizens: alphabetical list 549 Appendix 5. Minerals (n = 128) discovered elsewhere than in France and named after French citizens: chronological listing 552 Appendix 6. Minerals discovered elsewhere than in France and named after French citizens: geographic distribution 553 Appendix 7. The top 21 countries ranked according to the number of new mineral species discovered 556 Appendix 8. -
A Partial Glossary of Spanish Geological Terms Exclusive of Most Cognates
U.S. DEPARTMENT OF THE INTERIOR U.S. GEOLOGICAL SURVEY A Partial Glossary of Spanish Geological Terms Exclusive of Most Cognates by Keith R. Long Open-File Report 91-0579 This report is preliminary and has not been reviewed for conformity with U.S. Geological Survey editorial standards or with the North American Stratigraphic Code. Any use of trade, firm, or product names is for descriptive purposes only and does not imply endorsement by the U.S. Government. 1991 Preface In recent years, almost all countries in Latin America have adopted democratic political systems and liberal economic policies. The resulting favorable investment climate has spurred a new wave of North American investment in Latin American mineral resources and has improved cooperation between geoscience organizations on both continents. The U.S. Geological Survey (USGS) has responded to the new situation through cooperative mineral resource investigations with a number of countries in Latin America. These activities are now being coordinated by the USGS's Center for Inter-American Mineral Resource Investigations (CIMRI), recently established in Tucson, Arizona. In the course of CIMRI's work, we have found a need for a compilation of Spanish geological and mining terminology that goes beyond the few Spanish-English geological dictionaries available. Even geologists who are fluent in Spanish often encounter local terminology oijerga that is unfamiliar. These terms, which have grown out of five centuries of mining tradition in Latin America, and frequently draw on native languages, usually cannot be found in standard dictionaries. There are, of course, many geological terms which can be recognized even by geologists who speak little or no Spanish. -
AFM Study of the Epitaxial Growth of Brushite (Cahpo4.2H2O) On
American Mineralogist, Volume 95, pages 1747–1757, 2010 AFM study of the epitaxial growth of brushite (CaHPO4·2H2O) on gypsum cleavage surfaces ANDRÉ JORGE PINTO ,1 ENC A RN A CIÓN RUIZ -AGUDO ,2,* CHRISTINE V. PUTNIS ,2 ANDREW PUTNIS ,2 AM A LI A JIMÉNEZ ,1 A ND MA NUEL PRIETO 1 1Department of Geology, Universidad de Oviedo, Jesús Arias de Velasco s/n, 33005 Oviedo, Spain 2Institut für Mineralogie, Universität Münster, Corrensstrasse 24, 48149 Münster, Germany ABSTR A CT The epitaxial overgrowth of brushite (CaHPO4·2H2O) by the interaction of phosphate-bearing, slightly acidic, aqueous solutions with gypsum (CaSO4·2H2O) was investigated in situ using atomic force microscopy (AFM). Brushite growth nuclei were not observed to form on the {010} gypsum cleavage surface, but instead formed in areas of high dissolution, laterally attached to gypsum [101] step edges. During the brushite overgrowth the structural relationships between brushite (Aa) and gyp- sum (A2/a) result in several phenomena, including the development of induced twofold twining, habit polarity, and topographic effects due to coalescence of like-oriented crystals. The observed brushite growth is markedly anisotropic, with the growth rate along the main periodic bond chains (PBCs) in the brushite structure increasing in the order [101] > [101] > [010], leading to tabular forms elongated on [101]. Such a growth habit may result from the stabilization of the polar [101] direction of brushite due to changes in hydration of calcium ions induced by the presence of sulfate in solution, which is 2– consistent with the stabilization of the gypsum [101] steps during dissolution in the presence of HPO4 ions. -
New Mineral Names*
The American Mineralogist, Volume60, pages945-947, l9Z5 NEW MINERAL NAMES* Mlcttnrl FLerscurn AND J. A. MnuonRrNo Brassite* The mineral,associated with realgar,native As, and a little orpi- FneNcors FoNTAN,Mencsl Onlrnc, FnnNcors prnurNcrer, ment,occurs as grains up to 0.2mm in calciteveinlets in marlsand RoleNo Prrnnor, nNo RsleNr Sre,nr_(1973) La brassite, siliceouslimestones at Duranus,Alpes-Maritimes, France. MgHAsO..4HrO. Bull. Soc. Franc. Mineral. Cristallogr. 96, The nameis for the locality.Type materialis at the EcoleNatl. 365-370. Superieuredes Mines, Paris.M.F. Analysisby M.O. on 15.4mg from Jachymovgave AsrOr 4g.1, Jagowerite* MgO 15.6,CaO 0.9, HrO (by ditr.)35.4 percent, corresponding to the formula above.The mineralcan be synthesizedfrom solutions E. P. Mencsen,M. E. Conrns,AND A. E.Ano (1973)Jagowerite: with pH 24 andis readilyobtained by the spontaneousdehydra- A new barium phosphatemineral from the yukon Territory. tion of roesslerite.The Drl curve showsa small endothermic Can. Mineral. 12, 135-136. breakat 95o,a largeone at 135o,and an exothermiipeak at 570.. A gravimetricanalysis (H. Sharples,analyst) gave: BaO 38.41, X-ray studyshows the mineralto be orthorhombic,space group P,O631.41, Al,Os 25.87, Fe,O, 0.26, S 0.15,H,O+ 4.09,total Pbca,a 7.472+0.001,,l0.E9l +0.001, c 16.585+0.005A,Z:8. c 100.19percent. Emission and solid sourcemass spectrographic ca1c.2.326,meas 2.28*0.04 (data on syntheticcrystals, Brasse and analysesindicated the followingelems,rts present in amountsless Pemy,Bull. Soc. Chim. Franc.