Summary of Results. Re–Os Molybdenite Dating of Copper And
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A Review of Flotation Separation of Mg Carbonates (Dolomite and Magnesite)
minerals Review A Review of Flotation Separation of Mg Carbonates (Dolomite and Magnesite) Darius G. Wonyen 1,†, Varney Kromah 1,†, Borbor Gibson 1,† ID , Solomon Nah 1,† and Saeed Chehreh Chelgani 1,2,* ID 1 Department of Geology and Mining Engineering, Faculty of Engineering, University of Liberia, P.O. Box 9020 Monrovia, Liberia; [email protected] (D.G.W.); [email protected] (Y.K.); [email protected] (B.G.); [email protected] (S.N.) 2 Department of Electrical Engineering and Computer Science, University of Michigan, Ann Arbor, MI 48109, USA * Correspondence: [email protected]; Tel.: +1-41-6830-9356 † These authors contributed equally to the study. Received: 24 July 2018; Accepted: 13 August 2018; Published: 15 August 2018 Abstract: It is well documented that flotation has high economic viability for the beneficiation of valuable minerals when their main ore bodies contain magnesium (Mg) carbonates such as dolomite and magnesite. Flotation separation of Mg carbonates from their associated valuable minerals (AVMs) presents several challenges, and Mg carbonates have high levels of adverse effects on separation efficiency. These complexities can be attributed to various reasons: Mg carbonates are naturally hydrophilic, soluble, and exhibit similar surface characteristics as their AVMs. This study presents a compilation of various parameters, including zeta potential, pH, particle size, reagents (collectors, depressant, and modifiers), and bio-flotation, which were examined in several investigations into separating Mg carbonates from their AVMs by froth flotation. Keywords: dolomite; magnesite; flotation; bio-flotation 1. Introduction Magnesium (Mg) carbonates (salt-type minerals) are typical gangue phases associated with several valuable minerals, and have complicated processing [1,2]. -
Download PDF About Minerals Sorted by Mineral Name
MINERALS SORTED BY NAME Here is an alphabetical list of minerals discussed on this site. More information on and photographs of these minerals in Kentucky is available in the book “Rocks and Minerals of Kentucky” (Anderson, 1994). APATITE Crystal system: hexagonal. Fracture: conchoidal. Color: red, brown, white. Hardness: 5.0. Luster: opaque or semitransparent. Specific gravity: 3.1. Apatite, also called cellophane, occurs in peridotites in eastern and western Kentucky. A microcrystalline variety of collophane found in northern Woodford County is dark reddish brown, porous, and occurs in phosphatic beds, lenses, and nodules in the Tanglewood Member of the Lexington Limestone. Some fossils in the Tanglewood Member are coated with phosphate. Beds are generally very thin, but occasionally several feet thick. The Woodford County phosphate beds were mined during the early 1900s near Wallace, Ky. BARITE Crystal system: orthorhombic. Cleavage: often in groups of platy or tabular crystals. Color: usually white, but may be light shades of blue, brown, yellow, or red. Hardness: 3.0 to 3.5. Streak: white. Luster: vitreous to pearly. Specific gravity: 4.5. Tenacity: brittle. Uses: in heavy muds in oil-well drilling, to increase brilliance in the glass-making industry, as filler for paper, cosmetics, textiles, linoleum, rubber goods, paints. Barite generally occurs in a white massive variety (often appearing earthy when weathered), although some clear to bluish, bladed barite crystals have been observed in several vein deposits in central Kentucky, and commonly occurs as a solid solution series with celestite where barium and strontium can substitute for each other. Various nodular zones have been observed in Silurian–Devonian rocks in east-central Kentucky. -
Overview of Tungsten Indicator Minerals Scheelite and Wolframite with Examples from the Sisson W-Mo Deposit, Canada
Overview of tungsten indicator minerals scheelite and wolframite with examples from the Sisson W-Mo deposit, Canada M. Beth McClenaghan1, M.A. Parkhill2, A.A. Seaman3, A.G. Pronk3, M. McCurdy1 & D.J. Kontak4 1Geological Survey of Canada, 601 Booth Street, Ottawa, Ontario, Canada K1A 0E8 (e-mail: [email protected]) 2New Brunswick Department of Energy and Mines, Geological Surveys Branch, P.O. Box 50, Bathurst, New Brunswick, Canada E2A 3Z1 3New Brunswick Department of Energy and Mines, Geological Surveys Branch, P.O. Box 6000, Fredericton, New Brunswick, Canada E3B 5H1 4Department of Earth Sciences, Laurentian University, Sudbury, Ontario, Canada P3E 2C6 These short course notes provide an overview of published lit- Table 1. List of regional surveys and case studies conducted around erature on the use of scheelite and wolframite as indicator min- the world in which scheelite and/or wolframite in surficial sediments erals for W, Mo, and Au exploration. The use of scheelite and have been used as indicator minerals. wolframite in stream sediments is well documented for mineral Mineral Media Location Source of Information exploration but less so for using glacial sediments (Table 1). scheelite stream sediments Pakistan Asrarullah (1982) wolframite stream sediments Burma ESCAP Scretariat (1982) The Geological Survey of Canada has recently conducted a scheelite, wolframite stream sediments USA Theobald & Thompson (1960) glacial till and stream sediment indicator mineral case study scheelite stream sediments, soil Thailand Silakul (1986) around the Sisson W-Mo deposit in eastern Canada. scheelite stream sediments Greenland Hallenstein et al. (1981) Preliminary indicator mineral results from this ongoing study scheelite stream sediments Spain Fernández-Turiel et al. -
Porphyry and Other Molybdenum Deposits of Idaho and Montana
Porphyry and Other Molybdenum Deposits of Idaho and Montana Joseph E. Worthington Idaho Geological Survey University of Idaho Technical Report 07-3 Moscow, Idaho ISBN 1-55765-515-4 CONTENTS Introduction ................................................................................................ 1 Molybdenum Vein Deposits ...................................................................... 2 Tertiary Molybdenum Deposits ................................................................. 2 Little Falls—1 ............................................................................. 3 CUMO—2 .................................................................................. 3 Red Mountain Prospect—45 ...................................................... 3 Rocky Bar District—43 .............................................................. 3 West Eight Mile—37 .................................................................. 3 Devil’s Creek Prospect—46 ....................................................... 3 Walton—8 .................................................................................. 4 Ima—3 ........................................................................................ 4 Liver Peak (a.k.a. Goat Creek)—4 ............................................. 4 Bald Butte—5 ............................................................................. 5 Big Ben—6 ................................................................................. 6 Emigrant Gulch—7 ................................................................... -
Geology of Tungsten Deposits in North-Central Chile
UNITED STATES DEPARTMENT OF THE INTERIOR J. A. Krug, Secretary GEOLOGICAL SURVEY W. E. Wrather, Director Bulletin 960-C GEOLOGY OF TUNGSTEN DEPOSITS IN NORTH-CENTRAL CHILE BY JAMES F. McALLISTER AND CARLOS RUIZ F. Prepared in cooperation with the DEPARTAMENTO DE MINAS Y PETROLED DE CHILE under the auspices of INTERDEPARTMENTAL COMMITTEE ON SCIENTIFIC AND CULTURAL COOPERATION, DEPARTMENT OF STATE Geologic Investigations in the American Republics, 1947 (Pages 89-108) UNITED STATES GOVERNMENT PRINTING OFFICE WASHINGTON : 1948 For sale by the Superintendent of Documents, U. S. Government Printing Office, Washington 25, D. C. Price $1.75 CONTENTS Page Abstract____..______________________________._ 89 Introduction___________________________-__________ __________-___ 89 Geology_________________________________..._ 92 Rocks.____________________________________ 92 Structure____________________________________ 92 Minerals. _.---_.----_..---_.------_- _- -- 92 Type, size, and grade of ore deposits.------------._-----_-_-_-_-_ 93 Descriptions of mining properties__________-___-_-_-_---__--_---____- 94 Salamanca region____________________________________________ 94 Castaneda de Llamuco mine--___----------_-------_------__ 94 Picbe prospect... ________.- _ . 97 Domeyko region_______________________________________________ 97 El Durazno district.-..__-___.___--_____-__________...___ 97 Boliviana mine-..._________-____-._--._._-__-_--__-__. 99 Minillas property......____________________________________ 99 Vallenar region______________________________________________ 101 San Antonio mining property.______________________________ 102 Zapallo de Chehuque mining property_________*____-______- 104 Metric equivalents____-____-_____-_______-----_-__--_-_-_-__--_-- 106 Index.--.___-____-_._______________._______________ 107 Page PLATE 21. Geologic map of the Castaneda de Llamuco tungsten deposit. In pocket 22. Plan of workings, Castafieda de Llamuco mine. _-____-___ In pocket 23. -
Implications for Environmental and Economic Geology
UNIVERSITY OF CALIFORNIA RIVERSIDE Kinetics of the Dissolution of Scheelite in Groundwater: Implications for Environmental and Economic Geology A Thesis submitted in partial satisfaction of the requirements for the degree of Master of Science in Geological Sciences by Stephanie Danielle Montgomery March 2013 Thesis Committee: Dr. Michael A. McKibben, Chairperson Dr. Christopher Amrhein Dr. Timothy Lyons Copyright by Stephanie Danielle Montgomery 2013 The Thesis of Stephanie Danielle Montgomery is approved: _________________________________________ _________________________________________ _________________________________________ Committee Chairperson University of California, Riverside ABSTRACT OF THE THESIS Kinetics of the Dissolution of Scheelite in Groundwater: Implications for Environmental and Economic geology by Stephanie Danielle Montgomery Masters of Science, Graduate Program in Geological Sciences University of California, Riverside, March 2013 Dr. Michael McKibben, Chairperson Tungsten, an emerging contaminant, has no EPA standard for its permissible levels in drinking water. At sites in California, Nevada, and Arizona there may be a correlation between elevated levels of tungsten in drinking water and clusters of childhood acute lymphocytic leukemia (ALL). Developing a better understanding of how tungsten is released from rocks into surface and groundwater is therefore of growing environmental interest. Knowledge of tungstate ore mineral weathering processes, particularly the rates of dissolution of scheelite (CaWO4) in groundwater, could improve models of how tungsten is released and transported in natural waters. Our research focused on the experimental determination of the rates and products of scheelite dissolution in 0.01 M NaCl (a proxy for groundwater), as a function of temperature, pH, and mineral surface area. Batch reactor experiments were conducted within constant temperature circulation baths over a pH range of 3-10.5. -
Seg Sp-2 Giant Ore Deposits 285
SEG SP-2 GIANT ORE DEPOSITS 285 THE GENESIS OF GIANT PORPHYRY MOLYBDENUM DEPOSITS J. D. Keith, E. H. Christiansen Department of Geology, Brigham Young University Provo, Utah U.S.A., 84604 and R. B. Carten U. S. Geological Survey, Mackay School of Mines Reno, Nevada U.S.A., 89557-0047 ABSTRACT Giant porphyry molybdenum deposits are best exemplified by the Climax and Henderson deposits in Colorado. The high grades of these deposits are probably inherited from magmatic molybdenum concentrations of about 4 to 5 ppm, which are high for metaluminous rhyolitic magmas that average about 2 ppm molybdenum. High magmatic molybdenum concentrations in metaluminous rocks appear to be related to high magmatic oxygen fugacities (2 or 3 log units above QFM oxygen buffer) and are correlated with high niobium concentrations. High oxygen fugacities are likely inherited from calc-alkaline or lamprophyric predecessors. High niobium and molybdenum are related to extreme fractionation of rhyolitic magmas. Much higher concentrations of molybdenum (> 1,000 ppm) in the ore fluid (and the cupola magma) are probably achieved by crystallization in the deeper portions of a magma chamber accompanied by convection of the evolved liquid to the cupola and volatile fluxing. Exploration criteria for a giant, high-grade deposit include: 1) a tectonic setting that indicates a changeover from compressional to extensional tectonics, 2) thick continental crust at the time of deposit formation may encourage extreme differentiationand crustal contamination, 3) an isotopically zoned magma chamber indicative of a long-lived heat source, 4) a large, sub-volcanic, central-vent ash flow/dome system that erupted less than 100 km3 of rhyolite, and 5) high niobium concentrations (> 75 ppm) in a subalkaline, magnetite-bearing rhyolite. -
Role of Sodium Carbonate in Scheelite Flotation – a Multi-Faceted Reagent
Helmholtz-Zentrum Dresden-Rossendorf (HZDR) Role of sodium carbonate in scheelite flotation – a multi-faceted reagent Kupka, N.; Rudolph, M.; Originally published: October 2018 Minerals Engineering 129(2018), 120-128 DOI: https://doi.org/10.1016/j.mineng.2018.09.005 Perma-Link to Publication Repository of HZDR: https://www.hzdr.de/publications/Publ-27114 Release of the secondary publication on the basis of the German Copyright Law § 38 Section 4. CC-BY-NC-ND 4.0 *Manuscript Click here to view linked References Role of sodium carbonate in scheelite flotation – a multi-faceted reagent 1 1,a 1 2 Nathalie Kupka ; Martin Rudolph 3 1 Helmholtz Institute Freiberg for Resource Technology, Helmholtz Zentrum Dresden-Rossendorf, Chemnitzer 4 Straße 40, 09599 Freiberg, Germany 5 a 6 [email protected] 7 8 Abstract 9 10 Even though sodium carbonate is a reagent frequently used in flotation, its role is mostly described as 11 a buffering pH modifier and a pulp dispersant. In the case of scheelite flotation, it has been hinted that 12 13 sodium carbonate improves both grade and/or recovery but the mechanism itself is ambiguous at best 14 or at least has not been distinctly reported in the literature. Furthermore, the addition of depressants 15 such as sodium silicate or quebracho could be triggering additional mechanisms. Through batch 16 flotation testwork on a skarn scheelite ore with high calcite content, single mineral flotation and 17 contact angle measurements, this article aims at demonstrating that sodium carbonate is a multi- 18 faceted reagent, which serves as a buffering pH modifier, a pulp dispersant precipitating calcium and 19 20 magnesium ions in suspension, a depressant for calcite and calcium silicates and also a promoter for 21 scheelite. -
Porphyry Deposits
PORPHYRY DEPOSITS W.D. SINCLAIR Geological Survey of Canada, 601 Booth St., Ottawa, Ontario, K1A 0E8 E-mail: [email protected] Definition Au (±Ag, Cu, Mo) Mo (±W, Sn) Porphyry deposits are large, low- to medium-grade W-Mo (±Bi, Sn) deposits in which primary (hypogene) ore minerals are dom- Sn (±W, Mo, Ag, Bi, Cu, Zn, In) inantly structurally controlled and which are spatially and Sn-Ag (±W, Cu, Zn, Mo, Bi) genetically related to felsic to intermediate porphyritic intru- Ag (±Au, Zn, Pb) sions (Kirkham, 1972). The large size and structural control (e.g., veins, vein sets, stockworks, fractures, 'crackled zones' For deposits with currently subeconomic grades and and breccia pipes) serve to distinguish porphyry deposits tonnages, subtypes are based on probable coproduct and from a variety of deposits that may be peripherally associat- byproduct metals, assuming that the deposits were econom- ed, including skarns, high-temperature mantos, breccia ic. pipes, peripheral mesothermal veins, and epithermal pre- Geographical Distribution cious-metal deposits. Secondary minerals may be developed in supergene-enriched zones in porphyry Cu deposits by weathering of primary sulphides. Such zones typically have Porphyry deposits occur throughout the world in a series significantly higher Cu grades, thereby enhancing the poten- of extensive, relatively narrow, linear metallogenic tial for economic exploitation. provinces (Fig. 1). They are predominantly associated with The following subtypes of porphyry deposits are Mesozoic to Cenozoic orogenic belts in western North and defined according to the metals that are essential to the eco- South America and around the western margin of the Pacific nomics of the deposit (metals that are byproducts or poten- Basin, particularly within the South East Asian Archipelago. -
Stable Isotope Studies of Quartz-Vein Type Tungsten Deposits in Dajishan Mine, Jiangxi Province, Southeast China
Stable Isotope Geochemistry: A Tribute to Samuel Epstein © The Geochemical Society, Special Publication No.3, 1991 Editors: H. P. Taylor, Jr., J. R. O'Neil and I. R. Kaplan Stable isotope studies of quartz-vein type tungsten deposits in Dajishan Mine, Jiangxi Province, Southeast China YUCH-NING SHIEH Department of Earth and Atmospheric Sciences, Purdue University, West Lafayette, IN 47907, U.S.A. and GUO-XIN ZHANG Institute of Geochemistry (Guangzhou Branch), Academia Sinica, Guangzhou, Guangdong 510640, People's Republic of China Abstract-The Dajishan tungsten deposits belong to the wolframite-quartz vein type. These occur as fissure-fillings in the contact zone between the Jurassic Yenshanian granites and Cambrian meta- sandstones and slates. Quartz, beryl, muscovite, wolframite, scheelite, and sulfides are the major minerals formed in the main stage of mineralization. Late-stage minerals include calcite, dolomite, quartz, fluorite, and scheelite (replacing wolframite). No granitic rocks are exposed at the surface, but drilling has revealed hidden granitic bodies ranging in composition from biotite granite and two- mica granite to muscovite granite and pegmatite. These may represent a differentiation series from a common magma. Exceedingly uniform 0180 values are found in the minerals from the main-stage veins: quartz = 11.1-12.7 (n = 27), muscovite = 8.4-10.0 (n = 22), wolframite = 4.1-5.3 (n = 15), scheelite = 4.2-5.5 (n = 4), suggesting that isotopic equilibrium apparently has attained and that relatively constant physico-chemical conditions prevailed throughout the main-stage of mineralization. Oxygen isotope fractionations for .quartz-wolframite, quartz-scheelite, and quartz-muscovite pairs give concordant isotopic temperatures of 320-390°C, consistent with results from fluid inclusion 018 oD studies. -
Geochemistry and Genesis of Beryl Crystals in the LCT Pegmatite Type, Ebrahim-Attar Mountain, Western Iran
minerals Article Geochemistry and Genesis of Beryl Crystals in the LCT Pegmatite Type, Ebrahim-Attar Mountain, Western Iran Narges Daneshvar 1 , Hossein Azizi 1,* , Yoshihiro Asahara 2 , Motohiro Tsuboi 3 , Masayo Minami 4 and Yousif O. Mohammad 5 1 Department of Mining Engineering, Faculty of Engineering, University of Kurdistan, Sanandaj 66177-15175, Iran; [email protected] 2 Department of Earth and Environmental Sciences, Graduate School of Environmental Studies, Nagoya University, Nagoya 464-8601, Japan; [email protected] 3 Department of Applied Chemistry for Environment, School of Biological and Environmental Sciences, Kwansei Gakuin University, Sanda 669-1337, Japan; [email protected] 4 Division for Chronological Research, Institute for Space-Earth Environmental Research, Nagoya University, Nagoya 464-8601, Japan; [email protected] 5 Department of Geology, College of Science, Sulaimani University, Sulaimani 46001, Iraq; [email protected] * Correspondence: [email protected]; Tel.: +98-918-872-3794 Abstract: Ebrahim-Attar granitic pegmatite, which is distributed in southwest Ghorveh, western Iran, is strongly peraluminous and contains minor beryl crystals. Pale-green to white beryl grains are crystallized in the rim and central parts of the granite body. The beryl grains are characterized by low contents of alkali oxides (Na2O = 0.24–0.41 wt.%, K2O = 0.05–0.17 wt.%, Li2O = 0.03–0.04 wt.%, Citation: Daneshvar, N.; Azizi, H.; and Cs2O = 0.01–0.03 wt.%) and high contents of Be2O oxide (10.0 to 11.9 wt.%). The low contents Asahara, Y.; Tsuboi, M.; Minami, M.; of alkali elements (oxides), low Na/Li (apfu) ratios (2.94 to 5.75), and variations in iron oxide Mohammad, Y.O. -
Rhenium and Other Trace Elements in Molybdenite from the Christmas Mine Area, Gila County, Arizona
UNITED STATES DEPARTMENT OF THE INTERIOR GEOLOGICAL SURVEY Rhenium and Other Trace Elements in Molybdenite from the Christmas Mine Area, Gila County, Arizona Randolph A. Koski Open-File Report 81-154 This report is preliminary and has not been reviewed for conformity with U.S. Geological Survey editorial standards and stratigraphic nomenclature INTRODUCTION Rhenium (Re), the third-series transition metal with atomic number 75, is a rare element in the continental crust (0.0001 ppm according to Taylor, 1964) , but is concentrated especially in the mineral molybdenite , MoS_ Molybdenite from a variety of occurrences and mineral deposits in North America (for example, Fleischer, 1959; Giles and Schilling, 1972) and Australia (Riley, 1967; Morgan and others, 1968; and Ayres, 1974) has been analyzed previously and shows a wide range in Re content. Some geochemical trends are apparent: molybdenites from porphyry Cu-Mo deposits have high Re, whereas the content of Re in molybdenites from porphyry or stockwork Mo depos its is low. Five purified molybdenite samples from the Christmas mine area, Gila County, Arizona, have been analyzed by instrumental neutron activation to determine the variation in Re content within this porphyry copper system. In addition to Re, 13 other trace elements were detected in one or more of the samples. GEOLOGY OF THE CHRISTMAS DEPOSIT The Christmas porphyry copper deposit (Eastlick, 1968; Perry, 1969; and Koski, 1979) is centered on a Laramide-age, composite granodioritic stock and dike complex which intrudes Paleozoic carbonate rocks and mafic breccias and flows of the Cretaceous Williamson Canyon Volcanics in the sou thern Dripping Spring Mountains.