• Title/Summary/Keyword: metal ores

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Study of Utilization of Natural Zeolites as Functional Materials for Water Purification (II): Adsorption Properties of Heavy Metal Ions by Domestic Zeolites (천연 제올라이트의 수환경 개선용 기능성 소재로의 활용에 관한 연구 (II): 국내산 제올라이트의 중금속 이온 흡착 특성)

    • Journal of the Mineralogical Society of Korea
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    • v.16 no.3
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    • pp.201-213
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    • 2003
  • The adsorption property and ability of domestic zeolites for some heavy metal ions (Ag, Pb, Cr, Cu, Zn, Mn), which may cause a serious environmental problem in industrial wastewater, were evaluated on ore unit through a series of adsorption experiments together with careful examinations of mineral composition and properties of the zeolites. Though the adsorption behavior basically took place in the form of a cation exchange reaction, the higher CEC value does not necessarily to imply the higher adsorption capacity for a specific heavy metal. A general trend of the adsorption selectivity for heavy metals in the zeolites is determined to be as follow: $Ag\geq$Pb>Cr,Cu$\geq$Zn>Mn, but the adsorption properties of heavy metal ions somewhat depend on the species and composition of zeolite. Clinoptilolite tends to adsorb selectively Cu in case of Cr and Cu, whereas heulandite prefers Cr to Cu. A dominant adsorption selectivity of the zeolite ores for Ag and Pb is generally conspicuous regardless of their zeolite species and composition. The zeolite ores exhibit a preferential adsorption especially for $Ag^{+}$ so as not to regenerate when treated with $Na^{+}$ . In the adsorption capacity for heavy meta ions, the zeolites differ in great depending on their species: ferrierite>clinoptilolite>heulandite. Considering the CEC value of mordenite, the mordenite-rich ore appears to be similar to the clinoptilolite ore in the adsorption capacity. The adsorption capacity for heavy metals is not positively proportional to the CEC values of the zeolites measured by the exchange reaction with ammonium ion. In addition, the adsorption capacity roughly tends to depend on the zeolite contents, i.e., the grade of zeolite ore, but the trend is not consistent at all in some ores. These may be caused by the adsorption selectivity for some specific heavy metals, the presence of possible stacking micro-faults and natural cations such as K hardly to exchange in the zeolite. Considering the economic availability and functional effectiveness as natural zeolite resources, clinoptilolite ores could be applicable to utilize the domestic zeolites for the removal of heavy metals.

Chlorination of Metal Sulfide with Chlorine Gas (금속황화물의 염소화 반응)

  • Song, Yon-Ho;Hong, Jung-Seun;Lee, Chul-Tae
    • Applied Chemistry for Engineering
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    • v.5 no.6
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    • pp.1078-1091
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    • 1994
  • Thermodynamic calculations have been made from existing literature data to show that it is reasonable to expect to recover metal chlorides from the chlorination of metal sulfides with chlorine gas. The reactions between 12 metal sulfides, such as, $Ag_2S$, $As_2S_3$, CdS, CuS, $Cu_2S$, FeS, HgS, $MoS_2$, $Ni_3S_2$, PbS, $Sb_2S_3$ and chlorine gas were investigated by means of thermogravimetric method. The theorical calculation and the experimental investigation showed that chlorination of sulfide is a better alternative process for the extraction metallurgical process of sulfide ores.

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Mineralogical studies and extraction of some valuable elements from sulfide deposits of Abu Gurdi area, South Eastern Desert, Egypt

  • Ibrahim A. Salem;Gaafar A. El Bahariya;Bothina T. El Dosuky;Eman F. Refaey;Ahmed H. Ibrahim;Amr B. ElDeeb
    • Analytical Science and Technology
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    • v.37 no.1
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    • pp.47-62
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    • 2024
  • Abu Gurdi area is located in the South-eastern Desert of Egypt which considered as volcanic massive sulfide deposits (VMS). The present work aims at investigating the ore mineralogy of Abu Gurdi region in addition to the effectiveness of the hydrometallurgical route for processing these ores using alkaline leaching for the extraction of Zn, Cu, and Pb in the presence of hydrogen peroxide, has been investigated. The factors affecting the efficiency of the alkaline leaching of the used ore including the reagent composition, reagent concentration, leaching temperature, leaching time, and Solid /Liquid ratio, have been investigated. It was noted that the sulfide mineralization consists mainly of chalcopyrite, sphalerite, pyrite, galena and bornite. Gold is detected as rare, disseminated crystals within the gangue minerals. Under supergene conditions, secondary copper minerals (covellite, malachite, chrysocolla and atacamite) were formed. The maximum dissolution efficiencies of Cu, Zn, and Pb at the optimum leaching conditions i.e., 250 g/L NaCO3 - NaHCO3 alkali concentration, for 3 hr., at 250 ℃, and 1/5 Solid/liquid (S/L) ratio, were 99.48 %, 96.70 % and 99.11 %, respectively. An apparent activation energy for Zn, Cu and Pb dissolution were 21.599, 21.779 and 23.761 kJ.mol-1, respectively, which were between those of a typical diffusion-controlled process and a chemical reaction-controlled process. Hence, the diffusion of the solid product layer contributed more than the chemical reaction to control the rate of the leaching process. High pure Cu(OH)2, Pb(OH)2, and ZnCl2 were obtained from the finally obtained leach liquor at the optimum leaching conditions by precipitation at different pH. Finally, highly pure Au metal was separated from the mineralized massive sulfide via using adsorption method.

Ore Minerals and Mineralization Conditions of Magnetite Deposits in the Janggun Mine, Korea (장군광산(將軍鑛山)의 자철석광상(磁鐵石鑛床)에서 산출(産出)되는 광석광물(鑛石鑛物)과 생성조건(生成條件))

  • Lee, Hyun Koo;Lee, Chan Hee;Song, Suckhwan
    • Economic and Environmental Geology
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    • v.29 no.1
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    • pp.1-11
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    • 1996
  • Magnetite ores of the Janggun mine are embedded in dolomitic limestone of the Janggun Limestone Formation contacting with Chunyang granite, and are closely associated with skarn minerals. Mineralization of magnetite deposits can be divided into two stages as deep-seated skarn stage and shallow hydrothermal replacement stage. Mineralogies of skarn stage consist of magnetite, pyrrhotite and base-metal sulfides, and those of hydrothermal stage is base-metal sulfides, native bismuth, bismuthinite, tetrahedrite, boulangerite, bournonite and stannite. The FeS mole % in sphalerite and As atom % in arsenopyrite range from 22.47 to 26.30 and from 31.39 to 31.66 in skarn stage, and are from 17.54 to 32.54 and 28.87 to 30.70 in hydrothermal stage, respectively. Based on mineralization characteristics, mineral assemblages, chemical compositions and thermodynamic considerations, formation temperatures, sulfur fugacities ($-logf_2$), pH and oxygen fugacity ($-logfo_2$) estimated to be from 345 to $382^{\circ}C$, from 8.1 to 9.7atm, from 6.5 to 7.2 and from 30.5 to 31.2atm in the skarn stage, respectively, and temperature and $-logfs_2$ are from 245 to $315^{\circ}C$ and from 10.4 to 13.2atm in the hydrothermal stage.

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Ores and Fluid Inclusions from South Ore Deposits of the Dunjeon Gold Mine (둔전금광산(屯田金鑛山) 남광상(南鑛床)의 광석(鑛石)과 유체포유물(流體包有物))

  • Park, Hee-In;Woo, Young-Kyun;Lee, Chan Hee
    • Economic and Environmental Geology
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    • v.20 no.2
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    • pp.107-118
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    • 1987
  • The south ore deposits of the Dunjeon gold mine is a fissure-filling vein emplaced in the granitoids, skarnized and hornfelsified rocks of Ordovician Dumudong formation. The vein mineral paragenesis is complicated by repeated fracturing but three distinct depositional stages can be recognized; (1) base metal sulfides stage, (2) base metal sulfides, antimony-bismuthsulfosalts and native metals stage, (3) barren carbonates stage. Gold was mainly deposited in stage II. Fluid inclusion data indicate that fluid temperatures were from $310^{\circ}C$ to $402^{\circ}C$ during stage I and then declined steadily to $148^{\circ}C$ in the closing late stage III. Salinities were in the range of 0.4 to 5.0 equivalent weight percent NaCl and do not reveals any systematic trend through stag I, II and III. Ore mineralogy suggests that temperatures and sulfur fugacities in the earlier stage II were in the range of $340^{\circ}C$ to $360^{\circ}C$, $10^{-8}$ to $10^{-9}$ atm. respectively and then declined steadily to the range of $185^{\circ}C$ to $200^{\circ}C$ and $10^{-17}$ to $10^{-19}$atm. in the later stage II.

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Extractive Metallurgy and Recycling of Cobalt (코발트의 제련과 리사이클링)

  • Sohn, Ho-Sang
    • Journal of Powder Materials
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    • v.29 no.3
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    • pp.252-261
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    • 2022
  • Cobalt is a vital metal in the modern society because of its applications in lithium-ion batteries, super alloys, hard metals, and catalysts. Further, cobalt is a representative rare metal and is the 30th most abundant element in the Earth's crust. This study reviews the current status of cobalt extraction and recycling processes, along with the trends in its production amount and use. Although cobalt occurs in a wide range of minerals, such as oxides and sulfides of copper and nickel ores, the amounts of cobalt in the minerals are too low to be extracted economically. The Democratic Republic of Congo (DRC) leads cobalt mining, and accounts for 68.9 % of the global cobalt reserves (142,000 tons in 2020). Cobalt is mainly extracted from copper-cobalt and nickel-cobalt concentrates and is occasionally extracted directly from the ore itself by hydro-, pyro-, and electro-metallurgical processes. These smelting methods are essential for developing new recycling processes to extract cobalt from secondary resources. Cobalt is mainly recycled from lithium-ion batteries, spent catalysts, and cobalt alloys. The recycling methods for cobalt also depend on the type of secondary cobalt resource. Major recycling methods from secondary resources are applied in pyro- and hydrometallurgical processes.

Current Status of Pyrometallurgical Process for the Reclamation of Urban Ore (도시광석(都市鑛石) 재자원화(再資源化)를 위한 건식공정(乾式工程)의 현황(現況))

  • Kim, Byung-Su;Lee, Jae-Chun;Shin, Do-Yeoun;Jeoung, Jin-Ki;Rhee, Kang-In;Sohn, Jeong-Soo;Yang, Dong-Hyo;Kim, Min-Seuk;Kim, Soo-Kyung
    • Resources Recycling
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    • v.21 no.2
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    • pp.3-8
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    • 2012
  • In the points of the environmental conservation and the recirculating utilization of limited resources, it is very important to recover valuable metals like Au, Ag, Pd, Cu, Sn, Ni, Co, and Li used as industrial raw materials from urban ores. From now, many processes have been developed for recovering the valuable metals contained in urban ores and some of them have been operated commercially. In the paper, pyrometallurgical processes developed for reclaiming valuable metals from urban ores will be briefly introduced.

Hydrated Lime Roasting of Precious Metal Ores with A Cyclone Reactor

  • Cho, Chong S.
    • Proceedings of the Korea Association of Crystal Growth Conference
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    • 1997.06a
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    • pp.53-60
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    • 1997
  • The roasting of pyrite with a cyclone reactor have been studied in terms of investigating the reaction behavior of pyrite. The development of a fundamental model for pyrite oxidation and lime sulfation in a vertical cyclone reactor. The model assumes a chemical control shrinking core behavior for the pyrite and a fluid film control shrinking core behavior for the lime. The oxygen and sulphur dioxide concentrations and the energy balance for the gas, pyrite and lime particles are solved. The model was solved and characterized numerically. Experiments have been performed to study the influence of reaction parameters such as reactor temperatures, pyrite particle sizes, air flow rates, feeding rates, and mixing ratio of pyrite and lime. The oxidation and sulfation products were characterized chemically and physically.

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Silver Ores and Fluid Inclusions of the Cheolam Silver Deposits (철암은광상(鐵岩銀鑛床)의 광석(鑛石)과 유체포유물(流體包有物))

  • Park, Hee-In;Woo, Young-Kyun;Bae, Young Boo
    • Economic and Environmental Geology
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    • v.20 no.1
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    • pp.1-18
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    • 1987
  • The Cheolam silver deposits are emplaced along the fractures in breccia dike and the Hongjesa granite. Breccia dike contains fragments of late Cretaceous acidic volcanic rocks and other fragments of various rocks distributed in the mine area. Therefore it is presumed that the mineralization was taken place in later than late Cretaceous time. Mineral paragenesis is complicated by multiple episodes of fracturing. Six distinct depositional stages can be recognized: stage I, deposition of base metal sulfides; stage II, deposition of base metal sulfides and silver minerals; stage III, deposition of carbonates; stage IV, deposition of silver minerals and base metal sulfides; stage V, deposition of silver minerals; stage VI, deposition of barren quartz. Silver minerals from the deposits are native silver, acanthite, pyrargyrite, argentian tetrahedrite, stephanite, polybasite, pearceite, allargentum, antimonial silver and electrum. Fluid inclusion studies ware carried out for stage I, II, IV and VI quartz and stage III calcite. Homogenization temperatures for each stage are as follows: stage I, from $225^{\circ}$ to $360^{\circ}C$; stage II, from $145^{\circ}$ to $220^{\circ}C$; stage III, from $175^{\circ}$ to $240^{\circ}C$; stage IV, from $130^{\circ}$ to $185^{\circ}C$; stage VI, from $120^{\circ}$ to $145^{\circ}C$. Salinities of ore fluids were in the range of 4 and 10 wt.% equivalent NaCl over stage I and stage VI. Ore mineralogical data of each stage indicate that temperatures are within the range of homogenization temperature of fluid inclusions and sulfur fugacities declined steadily from $10^{-9.7}atm$. to $10^{-18.7}atm$. through stage I into stage V.

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Geochemical Study on Pollution of Heavy Metals in Soils, Plants and Streams in the Vicinity of Abandoned Metal Mines -Dalseong and Kyeongsan Mines- (금속폐광산주변의 토양, 식물 및 하천의 중금속오염에 대한 지화학적 연구 -달성 및 경산광산-)

  • Lee, Jae Yeong;Lee, In Ho;Lee, Sun Yeong
    • Economic and Environmental Geology
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    • v.29 no.5
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    • pp.597-613
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    • 1996
  • The tonnage of copper and tungsten produced at Dalseong mine by Taehan Tungsten Mining Company from 1961 to 1971 was 48,704 tons (M/T) of 4 wt.% Cu and 1,620 tons (S/T) of 70wt.% WO, but the mine was closed in 1974. Kyeongsan mine is a small abandoned cobalt mine with no data of production. To investigate the pollution level of the mine areas, soils, plants (Ohwi and Pampanini), stream waters and stream sediments were taken and Fe, Mn, Cu, Pb, Zn, Ni, Co, Cd and Cr were analysed by ICP. Soils are considerably contaminated by the heavy metals related to ore deposits, The heavy metal contents in plants vary with the species and parts of plants. Stream waters are anomalously high in heavy metals in the vicinity of the mines but the contents decrease downstream in the process of dilution and precipiation. However, heavy metal contents increase very high in stream sediments due to precipiation. To protect environmental damages caused by acid mine drainages wetlands must be constructed outside pits, and it is necessary to fill pits with waters, limestone chips and organic materials, which give reducing and alkaline condition to ores. Under the condition pyrite is protected from oxidation and aqueous iron sulphates precipitate to form stable secondary pyrite.

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