Origin of the Mineral Deposits
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Fundamental Flotation Behaviors of Chalcopyrite and Galena Using O-Isopropyl-N-Ethyl Thionocarbamate As a Collector
minerals Article Fundamental Flotation Behaviors of Chalcopyrite and Galena Using O-Isopropyl-N-Ethyl Thionocarbamate as a Collector Yongjie Bu ID , Yuehua Hu *, Wei Sun *, Zhiyong Gao ID and Runqing Liu School of Mineral Processing and Bioengineering, Central South University, Changsha 410083, China; [email protected] (Y.B.); [email protected] (Z.G.); [email protected] (R.L.) * Correspondence: [email protected] (Y.H.); [email protected] (W.S.); Tel.: +86-731-8830-482 (Y.H.); +86-0731-8883-6873 (W.S.) Received: 31 January 2018; Accepted: 12 March 2018; Published: 13 March 2018 Abstract: Copper and lead are two important and widely used metals in industry. Chalcopyrite (CuFeS2) is associated with galena (PbS) in ore, and it has been a research hotspot in separating galena from chalcopyrite by flotation. In this study, the flotation behaviors of chalcopyrite and galena were studied through flotation tests, adsorption measurements, solution chemistry calculation, Fourier transform infrared spectroscopy (FTIR) and molecular dynamics (MD) simulations. The results show that the floatability of chalcopyrite is better than that of galena in the presence of O-isopropyl-N-ethyl thionocarbamate (IPETC), and the recovery difference between chalcopyrite and galena is about 20% when IPETC is 7 × 10−4 mol/L at pH 9.5, while the floatability difference between the two minerals is significant. Competitive adsorption of OH− and IPETC on mineral surfaces leads to lower floatability of galena than that of chalcopyrite. IPETC is able to remove the hydration layer on mineral surfaces and then adsorb on active sites. The floatability of minerals is enhanced with the increase of their hydrophobicity. -
Editorial for Special Issue “Ore Genesis and Metamorphism: Geochemistry, Mineralogy, and Isotopes”
minerals Editorial Editorial for Special Issue “Ore Genesis and Metamorphism: Geochemistry, Mineralogy, and Isotopes” Pavel A. Serov Geological Institute of the Kola Science Centre, Russian Academy of Sciences, 184209 Apatity, Russia; [email protected] Magmatism, ore genesis and metamorphism are commonly associated processes that define fundamental features of the Earth’s crustal evolution from the earliest Precambrian to Phanerozoic. Basically, the need and importance of studying the role of metamorphic processes in formation and transformation of deposits is of great value when discussing the origin of deposits confined to varied geological settings. In synthesis, the signatures imprinted by metamorphic episodes during the evolution largely indicate complicated and multistage patterns of ore-forming processes, as well as the polygenic nature of the mineralization generated by magmatic, postmagmatic, and metamorphic processes. Rapid industrialization and expanding demand for various types of mineral raw ma- terials require increasing rates of mining operations. The current Special Issue is dedicated to the latest achievements in geochemistry, mineralogy, and geochronology of ore and metamorphic complexes, their interrelation, and the potential for further prospecting. The issue contains six practical and theoretical studies that provide for a better understanding of the age and nature of metamorphic and metasomatic transformations, as well as their contribution to mineralization in various geological complexes. The first article, by Jiang et al. [1], reports results of the first mineralogical–geochemical Citation: Serov, P.A. Editorial for studies of gem-quality nephrite from the major Yinggelike deposit (Xinjiang, NW China). Special Issue “Ore Genesis and The authors used a set of advanced analytical techniques, that is, electron probe microanaly- Metamorphism: Geochemistry, sis, X-ray fluorescence (XRF) spectrometry, inductively coupled plasma mass spectrometry Mineralogy, and Isotopes”. -
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]. -
A Column Leaching Model of Low-Grade Chalcopyrite Ore: Mineral Preferences and Chemical Reactivity
minerals Article A Column Leaching Model of Low-Grade Chalcopyrite Ore: Mineral Preferences and Chemical Reactivity Heike Bostelmann and Gordon Southam * School of Earth and Environmental Sciences, The University of Queensland, St Lucia 4072, Australia; [email protected] * Correspondence: [email protected]; Tel.: +61-07-3365-8505 Received: 16 November 2020; Accepted: 8 December 2020; Published: 17 December 2020 Abstract: Bioleaching models to examine copper extraction from low-grade chalcopyrite ores were set up to identify the influence of pyrite on leaching efficacy. A combination of scanning electron microscopy and geochemical analysis showed that extraction was marginally enhanced by the addition of pyrite when using a combination of Leptospirillum ferrooxidans, an iron oxidiser, Acidithiobacillus thiooxidans, a sulphur oxidising species and Acidithiobacillus ferrooxidans, an iron and sulphur oxidiser. Extensive biofilms formed on the pyrite surfaces (>106 cells/mm2) but were severely limited on chalcopyrite, possessing approximately the same number of cells as quartz grains, an internal non-nutrient control “substrate” (with ca. 2 103 cells/mm2). The presence of dissolved copper did × not inhibit the growth of this consortium. Indirect “bioleaching” of chalcopyrite appears to be limited by proton activity at the chalcopyrite surface. Keywords: bioleaching; chalcopyrite; pyrite; low-grade ore 1. Introduction Economic processing of chalcopyrite ores through bioleaching, i.e., the mobilisation of metals from ore by microorganisms, has not been as successful as secondary copper sulphide leaching operations [1]. This chalcopyrite “problem” needs to be solved, as it is the dominant copper mineral in many low-grade copper deposits. This has resulted in large quantities of low-grade waste material being stockpiled or discarded in mining operations, as they are not economic to process, though they do contain massive quantities of metals (i.e., copper) simply due to their combined volume [1–3]. -
United States Patent (19) 11 Patent Number: 4,514,290 Swiatkowski Et Al
United States Patent (19) 11 Patent Number: 4,514,290 Swiatkowski et al. 45 Date of Patent: Apr. 30, 1985 54 FLOTATION COLLECTOR COMPOSITION 4,206,045 6/1980 Wang et al.......................... 209/166 AND ITS USE 4,358,368 1/1982 Helsten et al........................ 252/61 4,425,229 1/1984 Baronet al. .......................... 252/61 (75) Inventors: Piotr Swiatkowski, Huddinge; Thomas Wiklund, Nacka, both of FOREIGN PATENT DOCUMENTS Sweden 1 155072 10/1963 Fed. Rep. of Germany ...... 209/167 73) Assignee: KenoGard AB, Stockholm, Sweden Primary Examiner-Bernard Nozick 21 Appl. No.: 471,006 Attorney, Agent, or Firm-Fred Philpitt 22 Filed: Mar. 1, 1983 57 ABSTRACT 30 Foreign Application Priority Data A flotation collector composition comprises a combina tion of fatty acids, amidocarboxylic acids or amidosul Mar. 5, 1982 SE Sweden ................................ 8201363 fonic acids and partial esters of phosphoric acid and 51 Int. Cl. ............................................... BO3D 1/14 alkoxylated alcohols. The collector composition is used 52 U.S. C. ....................................... 209/166; 252/61 for upgrading nonsulfide minerals containing alkaline 58) Field of Search ................... 252/61; 209/166, 167 earth metals by froth flotation. Minerals such as apatite, calcite, scheelite, fluorspar, magnesite and baryte can be 56) References Cited separated from the gangues using the collector compo U.S. PATENT DOCUMENTS sition. 2,297,664 9/1942 Tartaron ............................. 209/167 4,139,481 2/1979 Wang et al. ........................... 252A61 13 Claims, No Drawings 4,514,290 1. 2 The amidocarboxylic acids and the amidosulfonic FLOTATION COLLECTOR COMPOSITION AND acids which are used in the present collector combina ITS USE tions can be characterized by the general formula The present invention relates to a flotation collector R-X-(CH2)n-A, wherein x is the group composition comprising fatty acids, amido carboxylic acids or amidosulfonic acids and certain phosphate es R ters. -
Sedimentary Exhalative Deposits (SEDEX)
Sedimentary Exhalative Deposits (SEDEX) Main charactersitcs:SEDEX deposits are stratiform, massive sulphide lenses formed in local basins on the sea floor. This is usually as a result of hydrothermal activity in areas of continental rifting. They represent major sources of lead and zinc with minor amounts of gold, barium and copper. Alteration is common especially in the form of silicification. Sedex deposits have many similarities with VMS deposits. Idealised SEDEX Deposit Model e.g. Mount Isa, Broken Hill (Australia), Sullivan (Canada), Silvermines (Ireland) Adapted from Evans 1997: Ore Geology and Industrial Minerals The stratiform lenses formed in Sedex deposits can be up to 40km thick and have a lateral extent of 100km's. Stockwork or vein mineralisation may occur beneath this. Host rock lithology varies from shales, siltstones and carbonates (low energy environment) to debris flows, conglomerates and breccias (high energy environments). Sedex deposits have been categorised in terms of a sedimentary basin hierachy. First order basins have lateral extents of hundreds of km's and maybe represented by epicratonic embayments ot intracratonic basins. Second order basins which can be up to tens of km's in size occur within the first order basins and contain third order basins, less than 10km in diameter, where the stratiform sulphide lenses tend to develop. There are several ideas for the formation of these deposits but one contention is that they were formed by the convection of sea water as shown above. As the sea water traverses through the crust it would dissolve base metals from the host rock, which would eventually lead to their collection and precipitation near the surface. -
BOOM DAYS in HANCOCK COUNTY Or a History of Mining in the Towns of Hancock and Sullivan, Maine
BOOM DAYS IN HANCOCK COUNTY or A History of Mining in the Towns of Hancock and Sullivan, Maine By Henry B. Gallison U. of M. '35 As partial, fulfillment of the requirements of Ed 52 - History of Education in Maine. 2 . Foreword I must confess that in choosing this subject I did not expect to find so much material as I have succeeded in doing. I am not sorry; I am glad. I knew from hearsay and from the older folk of the region that there had been a great deal of excitement at one time, but I did known when the boom had taken place when I started my research. I had never heard of any report being published on the subject, and as a matter of fact, no comprehensive report has ever been written. Scattered reports on different phases of the work are here brought together for what I take to be the first time. All material used is source material, and I am only sorry that time will not allow me to go further than I have. The Library at Harvard College and the Library at Bowdoin both, contain reports which I should have like to read and incorporate into this report; and the Ellsworth American, a newspaper that was published weekly in Hancock County during those hectic days as well as at the present time, must have contained some truly classic stories about the boom. This narrative, then, must remain embellished by the personal incidents which would so liven it, and be only a statement of facts. -
Minerals and Mineral Products in Our Bedroom Bed Hematite
Minerals and Mineral Products in our Bedroom Make-Up Kit Muscovite Bed Talc Hematite: hinges, handles, Mica mattress springs Hematite: for color Chromite: chrome plating Bismuth Radio Barite Copper: wiring Plastic Pail Quartz: clock Mica Gold: connections Cassiterite: solder Toilet Bowl / Tub Closet Feldspar: porcelain Chromite: chrome plating Pyrolusite: coloring Hematite: hinges, handles (steel) Chromite: plumbing fixtures Quartz : mirror on door Copper: tubing Desk Toothpaste Hematite: hinges, handles (steel) Apatite: teeth Chromite: chrome plating Fluorite: toothpaste Mirror Rutile: to color false Hematite: handle, frame teeth yellow Chromite: plating Gold: fillings Gold: plating Cinnabar: fillings Quartz: mirror Towels Table Lamp Sphalerite: dyes Brass (an alloy of copper and Chromite: dyes zinc): base Quartz: bulb Water Pipe/Faucet/Shower bulb Wolframite: lamp filament Brass Copper: wiring Iron Nickel Minerals and Mineral Products in our Bedroom Chrome: stainless steel Bathroom Cleaner Department of Environment and Natural Resources Borax: abrasive, cleaner, and antiseptic MINES AND GEOSCIENCES BUREAU Deodorant Spray Can Cassiterite Chromite Copper Carpet Quartz Sphalerite: dyes Telephone Chromite: dyes Drinking Glasses Copper: wiring Sulfur: foam padding Quartz Chromite: plating Gold: red color Clock Silver: electronics Pentlandite: spring Graphite: batteries Refrigerator Quartz: glass, time keeper Hematite Television Chromite: stainless steel Chromite: plating Computer Galena Wolframite: monitor Wolframite: monitor Copper Copper: -
Download the Scanned
MTNERALOGTCALSOCIETY (LONDON) A meeting of the Society was held on Thursday, January 11th, 1951,in the apartments of the Geological Society of London, Burlington House, Piccadilly, W. 1 (by kind permis- sion). Exnrsrrs (1) Crystals of analcime and baryte from the trachyte of Traprain Law, East Lothian: by Dr. S. I. Tomkeiefi. (2) The use of a Laspeyres ocular lens in preference to the Berek compensator: by Dr. A. F. Hallimond. (3) Sections and colour photographs of (a) artificial corundum, (b) kyanite-staurolite intergrowth, (c) garnet: by Dr. Francis Jones. Papnns The following papers were read: (1) 'RnrcrmNlecn' AND 'BREZTNA'Leltrr,rln rN METEoRrrrc IRoNS. By Dr. L. J. Spencer Reichenbach lamellae, seen as bands on etched sections, were originally described as enclosed plates of troilite parallel to cube pianes in the kamacite-taenite structure, and Brczina lamellae as schreibersite parallel to the rhombic-dodecahedron. These minerals, and also cohenite, have since been observed in both of these and in other orientations. It has sometimes been assumed that bands at right angles indicate orientation on cube planes, but they may also be due to other orientations. On a section parallel to an octahedral plane it is possible only with lamellae parailel to the rhombic dodecahedron' (2) SnorrunNraRy INSLUSTSNSrN tnn IIvpnnsTHENE-GABBRo, ARDNAItrUR6HAN,ARGYLL- SIIIRE. By Mr. M. K. Wells The hypersthene-gabbro contains an abundance of granular basic hornfels inclusions which have all been interpreted in the past as recrystallized basic igneous rocks. Some of these inclusions, particularly banded ones, are now believed to be sedimentary rocks which have sufiered considerable metasomatism. -
Structure and Mineralization of Precambrian Rocks in the Galena-Roub Aix District, Black Hills, South Dakota
Structure and Mineralization of Precambrian Rocks in the \ Galena-Roubaix District, Black Hills, South Dakota ( By R. W. BAYLEY » CONTRIBUTIONS TO ECONOMIC GEOLOGY V ' GEOLOGICAL SURVEY BULLETIN 1312-E UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1970 UNITED STATES DEPARTMENT OF THE INTERIOR WALTER J. HICKEL, Secretary GEOLOGICAL SURVEY William T. Pecora, Director For sale by the Superintendent of Documents, U.S. Government Printing Office Washington, D.C. 20402 - Price 55 cents (paper cover) CONTENTS Page Abstract_ ____-_-_----_-----__--_-----_--_--.. El Introduction _________________________________ 1 Field methods_______-_____-_____-_____-__--_ 2 General geology.___-__--__-_--__-_--___._-_--_. 3 Stratigraphy. ___________________---__--__-__-.. 4 Metabasalt and chert.______-__-__-_____-_. 4 Graphitic schist and cherty ferruginous schist. 5 Metagraywacke, schist, and slate_ ___________ 6 Structure. ___________.-______-_-__-_-_-_-___-. 6 Distribution of gold. 7 Diamond drilling. __ 9 Magnetic survey. __ 10 Summary________ 14 References. -. ______ 15 ILLUSTEATIONS Page PLATE 1. Geologic map of the Galena-Roubaix district, Lawrence County, Black Hills, South Dakota.________________ In pocket FIGURE 1. Generalized geologic map of the northern Black Hills____-___ E2 2. Magnetic survey in the vicinity of U.S. Geological Survey diamond-drill hole 1__________________________________ 13 TABLE Page TABLIS 1. Results of core-sample analyses, U.S. Geological Survey diamond-drill hole 1, Galena-Roubaix district.____________ Ell ra CONTRIBUTIONS TO ECONOMIC GEOLOGY STRUCTURE AND MINERALIZATION OF PRECAMBRIAN ROCKS IN THE GALENA-ROUB AIX DISTRICT, BLACK HILLS, SOUTH DAKOTA ByK.W.BAYLEY ABSTRACT The Galena-Roubaix district is underlain chiefly by tightly folded and mod erately metamorphosed sedimentary and volcanic rocks of Precambrian age. -
The Electrical Resistivity of Galena, Pyrite, and Chalcopyrite
American Mineralogist, Volume61, pages248-259, 1976 The electricalresistivity of galena,pyrite, and chalcopyrite Doneln F. PnlorrronreNn RnlpH T. Suurv Departmentof Geologyand Geophysics,Uniuersity of Utah Salt Lake Cily, Utah 84112 Abstract. The sulfidesgalena, chalcopyrite, and pyrite are semiconductorswhose electrical resistivity and type are controlled by deviationsfrom stoichiometryand impurity content,and henceby their geochemicalenvironment. We measuredelectrical resistivity,type, and the impurity content (emissionspectrograph and microprobe) on small volumesof sample.Our results, together with those obtained from a comprehensiveliterature analysis, are usedto construct histogramsof the natural variability in carrier density and resistivity. Sulfur deficiency is the dominant defect in chalcopyrite and hence almost all natural samplesare n-type. lt appearsthat the copper/iron ratio is also important electrically,the copper-richsamples being the more resistive. lmportant donor deiectsin galena(z-type samples)are antimony and bismuth impurities, and sulfur vacancies;acceptor defects(p-type samples) include silver impurities and lead 'Mississippi vacancies.P-type samplesappear to be restrictedto Valley' and argentiferous deposits. In pyrite, electricallyactive impurities include cobalt, nickel, and copper as donors, and arsenicas an acceptor.Deviations from stoichiometry,in the same senseas galena,may be important. Pyritesfrom sedimentaryand epithermaldeposits are usuallyp-type if cupriferous sulfidesare not present.Samples from hypothermaldeposits -
Banded Iron Formations
Banded Iron Formations Cover Slide 1 What are Banded Iron Formations (BIFs)? • Large sedimentary structures Kalmina gorge banded iron (Gypsy Denise 2013, Creative Commons) BIFs were deposited in shallow marine troughs or basins. Deposits are tens of km long, several km wide and 150 – 600 m thick. Photo is of Kalmina gorge in the Pilbara (Karijini National Park, Hamersley Ranges) 2 What are Banded Iron Formations (BIFs)? • Large sedimentary structures • Bands of iron rich and iron poor rock Iron rich bands: hematite (Fe2O3), magnetite (Fe3O4), siderite (FeCO3) or pyrite (FeS2). Iron poor bands: chert (fine‐grained quartz) and low iron oxide levels Rock sample from a BIF (Woudloper 2009, Creative Commons 1.0) Iron rich bands are composed of hematitie (Fe2O3), magnetite (Fe3O4), siderite (FeCO3) or pyrite (FeS2). The iron poor bands contain chert (fine‐grained quartz) with lesser amounts of iron oxide. 3 What are Banded Iron Formations (BIFs)? • Large sedimentary structures • Bands of iron rich and iron poor rock • Archaean and Proterozoic in age BIF formation through time (KG Budge 2020, public domain) BIFs were deposited for 2 billion years during the Archaean and Proterozoic. There was another short time of deposition during a Snowball Earth event. 4 Why are BIFs important? • Iron ore exports are Australia’s top earner, worth $61 billion in 2017‐2018 • Iron ore comes from enriched BIF deposits Rio Tinto iron ore shiploader in the Pilbara (C Hargrave, CSIRO Science Image) Australia is consistently the leading iron ore exporter in the world. We have large deposits where the iron‐poor chert bands have been leached away, leaving 40%‐60% iron.