Some Magnetite Deposits of Stevens and Okanogan Counties, Washington
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Podiform Chromite Deposits—Database and Grade and Tonnage Models
Podiform Chromite Deposits—Database and Grade and Tonnage Models Scientific Investigations Report 2012–5157 U.S. Department of the Interior U.S. Geological Survey COVER View of the abandoned Chrome Concentrating Company mill, opened in 1917, near the No. 5 chromite mine in Del Puerto Canyon, Stanislaus County, California (USGS photograph by Dan Mosier, 1972). Insets show (upper right) specimen of massive chromite ore from the Pillikin mine, El Dorado County, California, and (lower left) specimen showing disseminated layers of chromite in dunite from the No. 5 mine, Stanislaus County, California (USGS photographs by Dan Mosier, 2012). Podiform Chromite Deposits—Database and Grade and Tonnage Models By Dan L. Mosier, Donald A. Singer, Barry C. Moring, and John P. Galloway Scientific Investigations Report 2012-5157 U.S. Department of the Interior U.S. Geological Survey U.S. Department of the Interior KEN SALAZAR, Secretary U.S. Geological Survey Marcia K. McNutt, Director U.S. Geological Survey, Reston, Virginia: 2012 This report and any updates to it are available online at: http://pubs.usgs.gov/sir/2012/5157/ For more information on the USGS—the Federal source for science about the Earth, its natural and living resources, natural hazards, and the environment—visit http://www.usgs.gov or call 1–888–ASK–USGS For an overview of USGS information products, including maps, imagery, and publications, visit http://www.usgs.gov/pubprod To order this and other USGS information products, visit http://store.usgs.gov Suggested citation: Mosier, D.L., Singer, D.A., Moring, B.C., and Galloway, J.P., 2012, Podiform chromite deposits—database and grade and tonnage models: U.S. -
The Efficient Improvement of Original Magnetite in Iron Ore Reduction
minerals Article The Efficient Improvement of Original Magnetite in Iron Ore Reduction Reaction in Magnetization Roasting Process and Mechanism Analysis by In Situ and Continuous Image Capture Bing Zhao 1,2, Peng Gao 1,2,*, Zhidong Tang 1,2 and Wuzhi Zhang 1,2 1 School of Resources and Civil Engineering, Northeastern University, Shenyang 110819, China; [email protected] (B.Z.); [email protected] (Z.T.); [email protected] (W.Z.) 2 National-Local Joint Engineering Research Center of High-Efficient Exploitation Technology for Refractory Iron Ore Resources, Shenyang 110819, China * Correspondence: [email protected]; Tel.: +86-024-8368-8920 Abstract: Magnetization roasting followed by magnetic separation is considered an effective method for recovering iron minerals. As hematite and magnetite are the main concomitant constituents in iron ores, the separation index after the magnetization roasting will be more optimized than with only hematite. In this research, the mechanism of the original magnetite improving iron ore reduction during the magnetization roasting process was explored using ore fines and lump ore samples. Under optimum roasting conditions, the iron grade increased from 62.17% to 65.22%, and iron recovery increased from 84.02% to 92.02% after separation, when Fe in the original magnetite content increased from 0.31% to 8.09%, although the Fe masses in each sample were equal. For lump ores with magnetite and hematite intergrowth, the method of in situ and continuous image capture Citation: Zhao, B.; Gao, P.; Tang, Z.; for microcrack generation and the evolution of the magnetization roasting process was innovatively Zhang, W. -
Recovery of Magnetite-Hematite Concentrate from Iron Ore Tailings
E3S Web of Conferences 247, 01042 (2021) https://doi.org/10.1051/e3sconf/202124701042 ICEPP-2021 Recovery of magnetite-hematite concentrate from iron ore tailings Mikhail Khokhulya1,*, Alexander Fomin1, and Svetlana Alekseeva1 1Mining Institute of Kola Science Center of Russian Academy of Sciences, Apatity, 184209, Russia Abstract. The research is aimed at study of the probable recovery of iron from the tailings of the Olcon mining company located in the north-western Arctic zone of Russia. Material composition of a sample from a tailings dump was analysed. The authors have developed a separation production technology to recover magnetite-hematite concentrate from the tailings. A processing flowsheet includes magnetic separation, milling and gravity concentration methods. The separation technology provides for production of iron ore concentrate with total iron content of 65.9% and recovers 91.0% of magnetite and 80.5% of hematite from the tailings containing 20.4% of total iron. The proposed technology will increase production of the concentrate at a dressing plant and reduce environmental impact. 1 Introduction The mineral processing plant of the Olcon JSC, located at the Murmansk region, produces magnetite- At present, there is an important problem worldwide in hematite concentrate. The processing technology the disposal of waste generated during the mineral includes several magnetic separation stages to produce production and processing. Tailings dumps occupy huge magnetite concentrate and two jigging stages to produce areas and pollute the environment. However, waste hematite concentrate from a non-magnetic fraction of material contains some valuable components that can be magnetic separation [13]. used in various industries. In the initial period of plant operation (since 1955) In Russia, mining-induced waste occupies more than iron ore tailings were stored in the Southern Bay of 300 thousand hectares of lands. -
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. -
Barite (Barium)
Barite (Barium) Chapter D of Critical Mineral Resources of the United States—Economic and Environmental Geology and Prospects for Future Supply Professional Paper 1802–D U.S. Department of the Interior U.S. Geological Survey Periodic Table of Elements 1A 8A 1 2 hydrogen helium 1.008 2A 3A 4A 5A 6A 7A 4.003 3 4 5 6 7 8 9 10 lithium beryllium boron carbon nitrogen oxygen fluorine neon 6.94 9.012 10.81 12.01 14.01 16.00 19.00 20.18 11 12 13 14 15 16 17 18 sodium magnesium aluminum silicon phosphorus sulfur chlorine argon 22.99 24.31 3B 4B 5B 6B 7B 8B 11B 12B 26.98 28.09 30.97 32.06 35.45 39.95 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 potassium calcium scandium titanium vanadium chromium manganese iron cobalt nickel copper zinc gallium germanium arsenic selenium bromine krypton 39.10 40.08 44.96 47.88 50.94 52.00 54.94 55.85 58.93 58.69 63.55 65.39 69.72 72.64 74.92 78.96 79.90 83.79 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 rubidium strontium yttrium zirconium niobium molybdenum technetium ruthenium rhodium palladium silver cadmium indium tin antimony tellurium iodine xenon 85.47 87.62 88.91 91.22 92.91 95.96 (98) 101.1 102.9 106.4 107.9 112.4 114.8 118.7 121.8 127.6 126.9 131.3 55 56 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 cesium barium hafnium tantalum tungsten rhenium osmium iridium platinum gold mercury thallium lead bismuth polonium astatine radon 132.9 137.3 178.5 180.9 183.9 186.2 190.2 192.2 195.1 197.0 200.5 204.4 207.2 209.0 (209) (210)(222) 87 88 104 105 106 107 108 109 110 111 112 113 114 115 116 -
Smelting Iron from Laterite: Technical Possibility Or Ethnographic Aberration?
Smelting Iron from Laterite: Technical Possibility or Ethnographic Aberration? T. O. PRYCE AND S. NATAPINTU introduction Laterites deposits (orlateriticsoilsastheyarealsocalled)arefrequently reported in Southeast Asia, and are ethnographically attested to have been used for the smelting of iron in the region (Abendanon 1917 in Bronson 1992:73; Bronson and Charoenwongsa 1986), as well as in Africa (Gordon and Killick 1993; Miller and Van Der Merwe 1994). The present authors do not dispute this evidence; we merely wish to counsel cautioninitsextrapolation.Modifyingour understanding of a population’s potential to locally produce their own iron has immediate ramifications for how we reconstruct ancient metal distribution net- works, and the social exchanges that have facilitated them since iron’s generally agreed appearance in Southeast Asian archaeological contexts during the mid-first millennium b.c. (e.g., Bellwood 2007:268; Higham 1989:190). We present this paper as a wholly constructive critique of what appears to be a prevailingperspectiveonpre-modernSoutheastAsianironmetallurgy.Wehave tried to avoid technical language and jargon wherever possible, as our aim is to motivate scholars working within the regiontogivefurtherconsiderationtoiron as a metal, as a technology, and as a socially significant medium (e.g., Appadurai 1998; Binsbergen 2005; Gosden and Marshall 1999). When writing a critique it is of course necessary to cite researchers with whom one disagrees, and we have done this with full acknowledgment that in modern archaeology no one person can encompass the entire knowledge spectrum of the discipline.1 The archaeome- tallurgy of iron is probably on the periphery of most of our colleagues’ interests, but sometimes, within the technical, lies the pivotal, and in sharing some of our insights we hope to illuminate issues of benefit to all researchers in Metal Age Southeast Asia. -
CHALCOPYRITE Visiting
communication, 2000). The quarry is privately owned and permission must be obtained before CHALCOPYRITE visiting. 13. Groveland mine, near Felch. CuFeS2 Common as attractive microcrystals (DeMark, A widespread and common copper ore mineral 2000). occurring in veins, disseminations, or as replacement deposits. Northern Peninsula. Alpena County: 1. Lafarge Corporation, Great Lakes Region (formerly National Gypsum Company) quarry, Alpena: Rare, with calcite, dolomite, barite, sphalerite, marcasite, pyrite, and strontianite (Morris, 1983). 2. Paxton quarry, Paxton: With calcite, dolomite, quartz, sphalerite, pyrite, and marcasite (Morris, 1983). Baraga County: Ohio mines (Webster and Imperial mines), Imperial Heights near Michigamme: Associates are apatite, goethite, grunerite, graphite, palygorskite, carbonates, and Figure 56: A 1.3 mm chalcopyrite crystal on dolomite other sulfides (Morris, 1983; DeMark, 2000). from the Groveland mine, Dickinson County. Ramon Crystals on calcite rhombohedra. DeMark specimen, Dan Behnke photograph. Dickinson County: 1. Metronite quarry, 4 km east-northeast of Felch: In tremolite marble Gogebic County: 1. Eureka mine near Ramsay, (Randville Dolomite) along contact of aplite- sections 12 and 13, T47N, R46W: With pyrite and pegmatite dike and in marginal parts of the dike gold in quartz veins at contact between granite and itself (Heinrich, 1962b). 2. Rian’s quarry southeast the Palms slate (Dickey and Young, 1938). 2. of Felch: Similar occurrence (Pratt, 1954). 3. In Copp’s mine 10 km north of Marenisco: With iron formation of the Menominee iron range and galena, sphalerite, pyrite, and dolomite (Dana, also just north of Felch: Rare, usually associated 1892). 3. Roadside exposure on south side of with secondary pyrite (Pratt, 1954; Brower, 1968). -
ITP Mining: Energy and Environmental Profile of the U.S. Mining Industry: Chapter 4: Iron
Energy and Environmental Profile of the U.S. Mining Industry 4 Iron The chemical element iron is the fourth most common element in the Earth's crust and the second most abundant metal. About five percent of the Earth's crust is composed of iron. The metal is chemically active and is found in nature combined with other elements in rocks and soils. In its natural state, iron is chemically bonded with oxygen, water, carbon dioxide, or sulfur in a variety of minerals. Forms of Iron Minerals, Ores, and Rocks Iron occurs mainly in iron-oxide ores. Some ores are a mixture of minerals rich in iron. Other iron ores are less rich and have a large number of impurities. The most important iron ore- forming minerals are: • Magnetite - Magnetite (Fe3O4) forms magnetic black iron ore. There are large deposits of magnetite in Russia and Sweden. • Hematite - Hematite (Fe2O3) is a red iron ore. Hematite occurs in almost all forms, from solid rock to loose earth. It is the most plentiful iron ore and occurs in large quantities throughout the world. • Goethite - Goethite (Fe2O3.H2O), a brown ore, contains iron. • Limonite - Limonite (Fe2O3.H2O) is a yellow-brown iron ore. Limonite is a collective term for impure goethite and a mixture of hydrated iron oxides. Iron 4-1 Energy and Environmental Profile of the U.S. Mining Industry Taconite contains low-grade iron in fine specks and bands. It is an extremely hard and flinty - containing about 25 - 30 percent iron. The iron in taconite occurs principally as magnetite and hematite and finely dispersed with silica in sedimentary deposits. -
Conservation and Systematic Development of Iron
1 PART : II INTRODUCTION CONSERVATION (PRESERVATION) AND SYSTEMATIC DEVELOPMENT OF IRON ORE One of the species of National Wealth is iron ore. Conservation of this mineral is of prime importance for industrial development. Indian legislature has recognized it in Section: 18 of the Mines & Minerals (Development & Regulation) Act, 1957. Section : 18, inter-alia, directs the Central Government to take all such steps as may be necessary for: (a) the conservation (Preservation) (b) and systematic development of minerals in India Systematic development of minerals in India would require: (a) exact estimate of reserves available (b) reasonable estimate of resources from where probable reserves can be estimated. This, inter–alia, would require opening of new mines. For that purpose, exploration is necessary. 2 For this, it would be worthwhile to refer to: A (REPORTS FOR EXPLORATION) (i) DOCUMENT ON STRATEGY FOR EXPLORATION, EXPLOITATION AND DEVELOPMENT FOR IRON ORE IN INDIA, PUBLISHED BY THE SUB–GROUP ON IRON ORE in India (January, 2006) (ii) MINERAL POLICY ISSUES IN THE CONTEXT OF EXPORT AND DOMESTIC USE OF IRON ORE IN INDIA - REPORT - FEBRUARY 2008 (INDIAN COUNCIL FOR RESEARCH ON INTERNATIONAL ECONOMIC RELATIONS) (iii) ECONOMICS OF SPONGE IRON AND STEEL PRODUCTION (SEPTEMBER, 2008) BY STEEL AND NATURAL RESOURCES STRATEGY RESEARCH, VASANT KUNJ, NEW DELHI (iv) IRON ORE – STATUS AND FUTURE PROSPECTS” by M. S. Jairam, Director, Geological Survey of India (v) IBM REPORT, 2009, AND PROVISIONAL FIGURES, AS ON 1-4-2010, SUPPLIED BY IBM, FOR IRON ORE 3 B (ILLEGAL MINING) (vi) 19TH REPORT OF STANDING COMMITTEE ON COAL & STEEL which highlights menace of illegal mining. -
CARBONATE and MAGNETITE PARAGENESES AS MONITORS of CARBON DIOXIDE and OXYGEN FUGACITY Andrea M
Lunar and Planetary Science XXXI 1424.pdf CARBONATE AND MAGNETITE PARAGENESES AS MONITORS OF CARBON DIOXIDE AND OXYGEN FUGACITY Andrea M. Koziol, Department of Geology, University of Dayton, 300 College Park, Dayton, OH 45469-2364 USA; e-mail: [email protected] Introduction: A geologist or meteoriticist magnetite grains, led Brearley to suggest that a may have before them an assemblage of miner- later reheating event caused the carbonate to als that together record a history of the tem- decompose. The CO2 evolved would produce perature, pressure, and fluid composition that the small voids. The siderite component of the the rock has experienced. Certain key minerals carbonate would preferentially break down, do record water, CO2, and O2 fugacities. forming magnetite [5]. Siderite, FeCO3, is one of those key miner- als. The stable coexistence of siderite with an- Alternatively, an increase in oxygen fugac- other key mineral, such as graphite or magnet- ity would promote magnetite formation by ite (Fe3O4), is only possible under certain re- strictive conditions. If other variables are 3 FeCO3 + 1/2 (O2) = Fe3O4 + 3 CO2. (1) known, the activity or fugacity of CO2 or O2 in the fluid phase once present in the rock can Oxygen fugacity could change as pore fluid often be estimated. This is an oxybarometer: a changes, or as certain mineral reactions pro- way of estimating oxygen fugacity (fO2) from gress. The oxygen may not be present in a gas mineral assemblages. The results can be used to phase, but may be dissolved in a fluid or supplied understand parageneses of iron-rich carbonate by a mineral. -
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. -
Rock and Mineral Identification for Engineers
Rock and Mineral Identification for Engineers November 1991 r~ u.s. Department of Transportation Federal Highway Administration acid bottle 8 granite ~~_k_nife _) v / muscovite 8 magnify~in_g . lens~ 0 09<2) Some common rocks, minerals, and identification aids (see text). Rock And Mineral Identification for Engineers TABLE OF CONTENTS Introduction ................................................................................ 1 Minerals ...................................................................................... 2 Rocks ........................................................................................... 6 Mineral Identification Procedure ............................................ 8 Rock Identification Procedure ............................................... 22 Engineering Properties of Rock Types ................................. 42 Summary ................................................................................... 49 Appendix: References ............................................................. 50 FIGURES 1. Moh's Hardness Scale ......................................................... 10 2. The Mineral Chert ............................................................... 16 3. The Mineral Quartz ............................................................. 16 4. The Mineral Plagioclase ...................................................... 17 5. The Minerals Orthoclase ..................................................... 17 6. The Mineral Hornblende ...................................................