VOLCANIC-ASSOCIATED MASSIVE SULFIDE DEPOSITS (MODELS 24A-B, 28A; Singer, 1986A,B; Cox, 1986)
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JAROSITE in ANCIENT TERRESTRIAL ROCKS: IMPLICATIONS for UNDERSTANDING MARS DIAGENESIS and HABITABILITY. S.L. Potter-Mcintyre1 and T.M
Lunar and Planetary Science XLVIII (2017) 1237.pdf JAROSITE IN ANCIENT TERRESTRIAL ROCKS: IMPLICATIONS FOR UNDERSTANDING MARS DIAGENESIS AND HABITABILITY. S.L. Potter-McIntyre1 and T.M. McCollom2, 1Southern Illinois University, Geology Department, Parkinson Lab Mailcode 4324, Carbondale, IL, 62901, [email protected], 2LASP, CU Boulder, 1234 Innovation Drive, Boulder, CO 80303. Introduction: Sulfate minerals of the alunite- jarosite family have been identified in stratified depos- its at numerous locations across Mars, including two of the rover landing sites [e.g., 1,2,3, 4]. Because these minerals typically precipitate from aqueous solutions and are stable only under acidic conditions, there has been considerable interest in studying their occurrence in martian settings as indicators of depositional and diagenetic conditions on early Mars [e.g., 3]. Many terrestrial occurrences of jarosite and alunite that have been proposed as analogs for these minerals have no clear relevance to the geologic setting where they occur on Mars. In southern Utah, however, Jurassic sand- stones at Mollies Nipple (MN) contain jarosite and alunite cements whose characteristics may be very sim- ilar to the stratified deposits on Mars. In addition, pre- vious studies have indicated these deposits to be spec- trally similar to many of the martian deposits [5,6]. Although the rocks at MN are early to middle Ju- rassic, the diagenetic history that resulted in the precip- itation of the jarosite and alunite cements is not under- stood. The results of the investigation will be used to gain insights into the origin and persistence of mineral from the alunite-jarosite family in martian settings. -
Geochemical Modeling of Iron and Aluminum Precipitation During Mixing and Neutralization of Acid Mine Drainage
minerals Article Geochemical Modeling of Iron and Aluminum Precipitation during Mixing and Neutralization of Acid Mine Drainage Darrell Kirk Nordstrom U.S. Geological Survey, Boulder, CO 80303, USA; [email protected] Received: 21 May 2020; Accepted: 14 June 2020; Published: 17 June 2020 Abstract: Geochemical modeling of precipitation reactions in the complex matrix of acid mine drainage is fundamental to understanding natural attenuation, lime treatment, and treatment procedures that separate constituents for potential reuse or recycling. The three main dissolved constituents in acid mine drainage are iron, aluminum, and sulfate. During the neutralization of acid mine drainage (AMD) by mixing with clean tributaries or by titration with a base such as sodium hydroxide or slaked lime, Ca(OH)2, iron precipitates at pH values of 2–3 if oxidized and aluminum precipitates at pH values of 4–5 and both processes buffer the pH during precipitation. Mixing processes were simulated using the ion-association model in the PHREEQC code. The results are sensitive to the solubility product constant (Ksp) used for the precipitating phases. A field example with data on discharge and water composition of AMD before and after mixing along with massive precipitation of an aluminum phase is simulated and shows that there is an optimal Ksp to give the best fit to the measured data. Best fit is defined when the predicted water composition after mixing and precipitation matches most closely the measured water chemistry. Slight adjustment to the proportion of stream discharges does not give a better fit. Keywords: geochemical modeling; acid mine drainage; iron and aluminum precipitation; schwertmannite; basaluminite 1. -
Review 1 Sb5+ and Sb3+ Substitution in Segnitite
1 Review 1 2 3 Sb5+ and Sb3+ substitution in segnitite: a new sink for As and Sb in the environment and 4 implications for acid mine drainage 5 6 Stuart J. Mills1, Barbara Etschmann2, Anthony R. Kampf3, Glenn Poirier4 & Matthew 7 Newville5 8 1Geosciences, Museum Victoria, GPO Box 666, Melbourne 3001, Victoria, Australia 9 2Mineralogy, South Australian Museum, North Terrace, Adelaide 5000 Australia + School of 10 Chemical Engineering, The University of Adelaide, North Terrace 5005, Australia 11 3Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 12 Exposition Boulevard, Los Angeles, California 90007, U.S.A. 13 4Mineral Sciences Division, Canadian Museum of Nature, P.O. Box 3443, Station D, Ottawa, 14 Ontario, Canada, K1P 6P4 15 5Center for Advanced Radiation Studies, University of Chicago, Building 434A, Argonne 16 National Laboratory, Argonne. IL 60439, U.S.A. 17 *E-mail: [email protected] 18 19 20 21 22 23 24 25 26 27 Abstract 28 A sample of Sb-rich segnitite from the Black Pine mine, Montana, USA has been studied by 29 microprobe analyses, single crystal X-ray diffraction, μ-EXAFS and XANES spectroscopy. 30 Linear combination fitting of the spectroscopic data provided Sb5+:Sb3+ = 85(2):15(2), where 31 Sb5+ is in octahedral coordination substituting for Fe3+ and Sb3+ is in tetrahedral coordination 32 substituting for As5+. Based upon this Sb5+:Sb3+ ratio, the microprobe analyses yielded the 33 empirical formula 3+ 5+ 2+ 5+ 3+ 6+ 34 Pb1.02H1.02(Fe 2.36Sb 0.41Cu 0.27)Σ3.04(As 1.78Sb 0.07S 0.02)Σ1.88O8(OH)6.00. -
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 -
Atomic Force Microscopy Studies on Sulfur-, Selenium- and Tellurium-Based Metal Chalcogenide Thin Films: a Review
Vol. 11(5), pp. 42-49, November 2017 DOI: 10.5897/AJPAC2017.0739 Article Number: BEB18A566732 African Journal of Pure and Applied ISSN 1996 - 0840 Copyright © 2017 Chemistry Author(s) retain the copyright of this article http://www.academicjournals.org/AJPAC Review Atomic force microscopy studies on sulfur-, selenium- and tellurium-based metal chalcogenide thin films: A review Ho Soonmin Centre for Green Chemistry and Applied Chemistry, INTI International University, Putra Nilai, 71800, Negeri Sembilan, Malaysia. Received 5 October, 2017; Accepted 16 November, 2017 Sulfur, selenium and tellurium-based metal chalcogenide films have been prepared using various deposition methods. Investigation of morphological properties of the generated surface structures on chalcogenide thin films using atomic force microscopy technique was reported. The purpose of this work is to describe past important research findings that are related to atomic force microscopy technique. Key words: Atomic force microscopy, surface roughness, film thickness, grain size. INTRODUCTION Sulfur-based films (Ho et al., 2013; Saravanan et al., epitaxy, metal organic vapor phase epitaxy, pulsed laser 2010; Mohd et al., 2011; Abdullah et al., 2010; deposition, spray pyrolysis, successive ionic layer Dhandayuthapani et al., 2017; Huse et al., 2017; Ahmad adsorption, and reaction. There are a number of papers et al., 2010; Garcia et al., 2017), selenium based films that report the results of morphological, structural, (Ham et al., 2008; Xue et al., 2006; Rajesh et al., 2013; compositional, functional group, and optical Kassim et al., 2010; Wen et al., 2017), and tellurium- characterization of thin films. These films were based metal chalcogenide films (Laxman et al., 2012; characterized using range of characterization techniques Pandiaraman et al., 2011; Camacho-Espinosa et al., such as X-ray photoelectron spectroscopy (Lisco et al., 2014; Chen et al., 2009; Yang et al., 2017) possess 2015; Meng et al., 2015; Zhang et al., 2001; useful electrical, optical and physical properties. -
UV-Shielding Properties of Fe (Jarosite) Vs. Ca (Gypsum) Sulphates
Astrobiological significance of minerals on Mars surface environment: UV-shielding properties of Fe (jarosite) vs. Ca (gypsum) sulphates Gabriel Amaral1, Jesus Martinez-Frias2, Luis Vázquez2,3 1 Departamento de Química Física I, Facultad de Ciencias Químicas, Universidad Complutense, 28040 Madrid, Spain; Tel: 34-91-394-4305/4321, Fax: 34-91-394-4135, e-mail: [email protected] 2 Centro de Astrobiología (CSIC-INTA), 28850 Torrejón de Ardoz, Madrid, Spain, Tel: 34-91-520-6418, Fax: 34-91-520-1621, e-mail: [email protected] 3 Departamento de Matemática Aplicada, Facultad de Informática, Universidad Complutense de Madrid, 28040 Madrid, Spain, Tel: +34-91-3947612, Fax: +34- 91-3947510, e-mail: [email protected] &RUUHVSRQGLQJDXWKRU Jesús Martinez-Frias ([email protected]) 1 $EVWUDFW The recent discovery of liquid water-related sulphates on Mars is of great astrobiological interest. UV radiation experiments, using natural Ca and Fe sulphates (gypsum, jarosite), coming from two selected areas of SE Spain (Jaroso Hydrothermal System and the Sorbas evaporitic basin), were performed using a Xe Lamp with an integrated output from 220 nm to 500 nm of 1.2 Wm-2. The results obtained demonstrate a large difference in the UV protection capabilities of both minerals and also confirm that the mineralogical composition of the Martian regolith is a crucial shielding factor. Whereas gypsum showed a much higher transmission percentage, jarosite samples, with a thickness of only 500 µm, prevented transmission. This result is extremely important for the search for life on Mars as: a) jarosite typically occurs on Earth as alteration crusts and patinas, and b) a very thin crust of jarosite on the surface of Mars would be sufficient to shield microorganisms from UV radiation. -
Gomposition and Occurrence of Electrum Atthe
L37 The Canadian M inerala g i st Vol.33,pp. 137-151(1995) GOMPOSITIONAND OCCURRENCEOF ELECTRUM ATTHE MORNINGSTAR DEPOSIT, SAN BERNARDINOCOUNTY, GALIFORNIA: EVIDENCEFOR REMOBILIZATION OF GOLD AND SILVER RONALD WYNN SIIEETS*, JAMES R. CRAIG em ROBERT J. BODNAR Depanmen of Geolngical Sciences, Virginin Polytechnic h stitate and Stale (Jniversity, 4A44 Dening Hall, Blacl<sburg, Virginin 24060, U.S-A,. Arsrnacr Elecfum, acanthiteand uytenbogaardtite have been examined from six depthswithin the tabular quartzt calcite sockwork and breccia-filled veins in the fault-zone-hostedMorning Star depositof the northeasternMojave Desert, Califomia. Six distinct types of electrum have been identified on the basis of minerat association,grain moryhology and composition. Two types, (1) p1'rite-hostedand (2) quartz-hostedelectrum, occur with acanthite after argentite and base-metalsulfide minerals in unoxidized portions of the orebody; the remaining forr types, (3) goethite-hostedelectrum, (4) electnrm cores, (5) electrumrims and (6) wire electrum,are associatedwith assemblagesof supergeneminerals in its oxidizedportions. Pyrite- hosted quartz-hostedand goethite-hostedelectrum range in compositionfrom 6l ta 75 utt.7oAu and have uniform textures and no zoning. In lower portions ofthe oxidized ore zone, electrum seemsto replacegoethite and occursas small grains on surfacesof the goethite.Textural evidencefavors supergeneremobilization of Au and Ag, which were depositedas electrum on or replacinggoethite. This type of electrumis identical in appearanceand compositionto prinary electrum,In the upper portions of the oxidized zone,secondary electum occursas a gold-rich rim on a core of elechum and as wire-like grains,both with acanthiteand uytenbogaardtite.Such secondaryelectrum contains from 78 to 93 wt./o Au. Textural relations and asso- ciated minerals suggestthat the primary electrum was hydrothermally depositedand partially remobilized by supergene processes. -
Mobilisation of Arsenic, Selenium and Uranium from Carboniferous Black Shales in West Ireland T ⁎ Joseph G.T
Applied Geochemistry 109 (2019) 104401 Contents lists available at ScienceDirect Applied Geochemistry journal homepage: www.elsevier.com/locate/apgeochem Mobilisation of arsenic, selenium and uranium from Carboniferous black shales in west Ireland T ⁎ Joseph G.T. Armstronga, , John Parnella, Liam A. Bullocka,b, Adrian J. Boycec, Magali Perezd, Jörg Feldmannd a School of Geosciences, University of Aberdeen, Meston Building, Aberdeen, AB24 3UE, UK b Ocean and Earth Science, National Oceanography Centre Southampton, University of Southampton Waterfront Campus, European Way, Southampton, SO14 3ZH, UK c Scottish Universities Environmental Research Centre, University of Glasgow, Rankine Avenue, Scottish Enterprise Technology Park, East Kilbride, Glasgow, G75 0QF, UK d Trace Element Speciation Laboratory, School of Natural and Computing Science, University of Aberdeen, Meston Building, Aberdeen, AB24 3UE, UK ARTICLE INFO ABSTRACT Editorial handling by Prof. M. Kersten The fixation and accumulation of critical elements in the near surface environment is an important factor in Keywords: understanding elemental cycling through the crust, both for exploration of new resources and environmental Black shale management strategies. Carbonaceous black shales are commonly rich in trace elements relative to global crustal Carboniferous averages, many of which have potential environmental impacts depending on their speciation and mobility at Regolith surface. This trace element mobility can be investigated by studying the secondary mineralisation (regolith) Secondary mineralisation associated with black shales at surface. In this study, Carboniferous shales on the west coast of Ireland are found Oxidation to have higher than average shale concentrations of As, Cd, Cu, Co, Mo, Ni, Se, Te and U, similar to the laterally Jarosite equivalent Bowland Shales, UK. -
Metal-Sulfur Compounds in N2 Reduction and Nitrogenase-Related Chemistry
Metal-Sulfur Compounds in N2 Reduction and Nitrogenase-Related Chemistry Kazuki Tanifuji1 and Yasuhiro Ohki 2* 1 Department of Molecular Biology and Biochemistry, University of California, Irvine, Irvine, CA 92697-3900, United States 2 Department of Chemsitry, Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8602, Japan e-mail: [email protected] Abstract Transition metal-sulfur (M-S) compounds are an indispensable means for biological systems to convert N2 into NH3 (biological N2 fixation), and these may have emerged by chemical evolution from a pre-biotic N2 fixation system. With a main focus on synthetic species, this article provides a comprehensive review of the chemistry of M-S compounds related to the conversion of N2 and the structures/functions of the nitrogenase cofactors. Three classes of M-S compounds are highlighted here: multi-nuclear M-S clusters structurally or functionally relevant to the nitrogenase cofactors; mono- and di-nuclear transition metal complexes supported by sulfur-containing ligands in N2 and N2Hx (x = 2, 4) chemistry; metal sulfide-based solid materials employed in the reduction of N2. Fair assessments on these classes of compounds revealed that our understanding is still limited in N2 reduction and related substrate reductions. Our aims of this review are to compile a collection of studies performed at atomic to mesoscopic scales and to present potential opportunities for elucidating the roles of metal and sulfur atoms in the biological N2 fixation that might be helpful -
Acanthite Ag2s C 2001-2005 Mineral Data Publishing, Version 1 Crystal Data: Monoclinic, Pseudo-Orthorhombic
Acanthite Ag2S c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic, pseudo-orthorhombic. Point Group: 2/m. Primary crystals are rare, prismatic to long prismatic, elongated along [001], to 2.5 cm, may be tubular; massive. Commonly paramorphic after the cubic high-temperature phase (“argentite”), of original cubic or octahedral habit, to 8 cm. Twinning: Polysynthetic on {111}, may be very complex due to inversion; contact on {101}. Physical Properties: Cleavage: Indistinct. Fracture: Uneven. Tenacity: Sectile. Hardness = 2.0–2.5 VHN = 21–25 (50 g load). D(meas.) = 7.20–7.22 D(calc.) = 7.24 Photosensitive. Optical Properties: Opaque. Color: Iron-black. Streak: Black. Luster: Metallic. Anisotropism: Weak. R: (400) 32.8, (420) 32.9, (440) 33.0, (460) 33.1, (480) 33.0, (500) 32.7, (520) 32.0, (540) 31.2, (560) 30.5, (580) 29.9, (600) 29.2, (620) 28.7, (640) 28.2, (660) 27.6, (680) 27.0, (700) 26.4 ◦ Cell Data: Space Group: P 21/n. a = 4.229 b = 6.931 c = 7.862 β =99.61 Z=4 X-ray Powder Pattern: Synthetic. 2.606 (100), 2.440 (80), 2.383 (75), 2.836 (70), 2.583 (70), 2.456 (70), 3.080 (60) Chemistry: (1) (2) (3) Ag 86.4 87.2 87.06 Cu 0.1 Se 1.6 S 12.0 12.6 12.94 Total 100.0 99.9 100.00 (1) Guanajuato, Mexico; by electron microprobe. (2) Santa Lucia mine, La Luz, Guanajuato, Mexico; by electron microprobe. (3) Ag2S. Polymorphism & Series: The high-temperature cubic form (“argentite”) inverts to acanthite at about 173 ◦C; below this temperature acanthite is the stable phase and forms directly. -
Aluminite Al2(SO4)(OH)4 • 7H2O C 2001-2005 Mineral Data Publishing, Version 1
Aluminite Al2(SO4)(OH)4 • 7H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. As needles and fibers, to 0.1 mm, commonly in reniform, nodular, or spherulitic masses, and as veinlets. Physical Properties: Fracture: Earthy, in aggregates. Tenacity: Friable. Hardness = 1–2 D(meas.) = 1.66–1.82 D(calc.) = 1.794 Optical Properties: Translucent, opaque if massive. Color: White to grayish white; colorless in transmitted light. Luster: Dull to earthy. Optical Class: Biaxial (+). Orientation: X = elongation. α = 1.459–1.460 β = 1.464 γ = 1.470 2V(meas.) = ∼90◦ Cell Data: Space Group: P 21/c. a = 7.440(1) b = 15.583(2) c = 11.700(2) β = 110.18(2)◦ Z=4 X-ray Powder Pattern: G´ant, Hungary. 7.93 (100), 9.01 (90), 3.7224 (72), 4.760 (71), 3.7419 (70), 5.033 (63), 4.868 (63) Chemistry: (1) (2) SO3 23.37 23.26 Al2O3 29.87 29.63 H2O 46.76 47.11 Total [100.00] 100.00 (1) Newhaven, England; recalculated to 100% after deduction of a small amount of gypsum. • (2) Al2(SO4)(OH)4 7H2O. Occurrence: Typically in clays or lignites, formed by the reaction of sulfate-bearing solutions from the decomposition of marcasite or pyrite at moderate temperatures with aluminous silicates; as a volcanic sublimate; in sulfur deposits; rarely in caves. Association: Basaluminite, gibbsite, epsomite, gypsum, celestine, dolomite, goethite. Distribution: In Germany, from Morl, near Halle, Saxony-Anhalt. In the Czech Republic, at Milevsko (M¨uhlhausen),near Kralupy, Kuchelbad, Miletic, and Velvary. -
The Use Op Cobalt-60 As a Radiotracer in a Study Op
THE USE OP COBALT-60 AS A RADIOTRACER IN A STUDY OP THE ANALYTICAL CHEMISTRY OF COBALT DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of the Ohio State University By DARNELL SALYER, B. S. The Ohio State University 1956 Approvec by: Adv^rer Department of Chemistry ACKNOWLEDGMENT The author would like to express his sincere appre ciation to Dr. T. R. Sweet for his guidance and advice during the period of this research. The author’s wife, Octavia Elizabeth Salyer, has been a source of help and encouragement during the con clusion of this work and the oreparation of the manuscript. Most of this work was completed while the author held graduate fellowships from the Cincinnati Chemical vVorks (1954-55) and the Central Division of the Allied Chemical and Dye Corporation (1955-56). The aid provided by these fellowsnips is gratefully acknowledged. ii Table of Contents Page INTRODUCTION ................................................ 1 THE ANODIC DEPOSITION PROBLEM........................... 9 Theory of Anodic Deposition ...................... 9 Conditions for the Deposition of C o b a l t ......... 13 Promising Methods, A Qualitative Study........... 16 Reproducibility, A Quantitative Study ........... 17 Nature of the Deposits................. ........... 27 Ignition of Deposits............................... 33 Summary of Optimum Conditions for Plating and Weighing...................................... 34 Preparation of the Standard Curve ................ 37 Interference Study.................................. 41 DETERMINATION OF SMALL AMOUNTS OF COBALT BY THE ISOTOPE DILUTION-ANODIC DEPOSITION' METHOD . 4 6 Separation of Cobalt from Iron............... 49 Conclusion................................... 49 A STUDY OF THE CATHODIC ElECTRODEPOSITION METHOD FOR oOBALT »»»»»••••»»»..»»•».»• 31 Previous W o r k ...................................... 53 Experimental.