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By Edgar Blanco

At the Deer Trail Mine, interest in recovering noble metals from oxide ore and tailings oxide ore with 6.0/1.0 g/t Au and 200/140 g/t Ag respectively has led to metallurgic studies focused on finding an adequate treatment for these materials. Using cyanide leaching, the silver/gold recoveries from oxide ore and oxide tailings were 39%/95% and 36%/96%, respectively. Since these recoveries were less than spectacular for silver, it was decided to explore a non-cyanide leaching process that would extract silver and gold better. Based on previous research the possibility of using aqua regia in combination with sulfuric acid was evaluated. On a laboratory scale, variables such as mineralogical composition, concentration of reagents, dissolved oxygen, reaction time, pH and temperature were evaluated. Under optimal conditions it was possible to achieve >65% silver recovery and >85% gold recovery for both oxide ore and tailings.

Jan 1, 2009

By J. E. Dutrizac

The mineral forms of silver, lead and cadmium in the zinc concentrates and the various roaster products made by the Kidd Creek Division of Falconbridge Inc. have been elucidated. In the concentrates, all three elements occur mainly in sulphide form, either in solid solution in the principal ore minerals or as discrete mineral grains. During roasting, Ag, Pb and Cd are preferentially concentrated in the hot cyclone and ESP dusts of the roaster train. Silver is converted to <0.5 µm grains of silver metal and to Ag2S04 which dissolves in or impregnates silicates. Lead is converted to Pb-bearing silicates or to PbS04 and PbO which are present either as tiny free grains in ZnO or as an intergrowth with lead silicate. Lead is also a minor constituent of the ferrite phase. Cadmium occurs mostly as cadmium-bearing zno and ZnFe2o4 , but a significant amount also reports as Cd-bearing silicates or zinc sulphate.

Jan 1, 1990

By Corby G. Anderson

For over a century, the Sunshine Mine in Idaho has been a major producer of silver. An estimated 335,000,000 troy ounces of silver has been mined. This has established the Sunshine Mine as the largest single source of silver in the world. Because the dominant silver containing mineral is tetrahedrite, a copper and antimony sulfide, normal metallurgical treatments to recover the precious metal are not practical. Thus, over the course of the company&apos;s history, novel, hydrometallurgical technologies have been developed on-site to handle complex, precious metal containing materials. Recently, the use of Sunshine technology has been extended to the recycle of secondary materials. As well, the use of Sunshine technology by other organizations for treatment of both primary and secondary feedstocks containing precious and base metals is an area of growing interest. This paper will provide an overview of Sunshine hydrometallurgical technologies including the applicability of Sunshine technology to the recycling of precious and base metals.

Jan 1, 1995

By Leonid N. Shekhter, Corby G. Anderson, Esra Cankaya-Yalcin, Daniel G. Gribbin, Joseph D. Lessard, Larry F. McHugh

"A new process for smelting copper, Looping Sulfide Oxidation™ (LSO™) significantly and positively alters the smelting energy balance. This process uses copper oxide in conjunction with air for the desulfurization of copper and chalcopyrite concentrates. Copper oxide is regenerated in a flash type furnace and then ""looped"" back for the oxidation of the copper concentrate. Heat and material balances show that the Looping Sulfide Oxidation™ process requires significantly lower net energy than conventional technology. This process produces anode copper and higher S02 content off-gases for efficient formation of sulfuric acid. Additionally, the process yields slags with lower copper solubility as compared to the conventional technology.IntroductionBased on the positive results from LSO™ investigations [1], further lab investigations into co=on sulfides and metal oxides were performed. It was discovered that chalcopyrite (CuFeS2) is oxidized with copper (II) oxide. In this reaction over 98.5% of sulfur was removed as S02, while a significantly improved energy balance was observed. This paper intends to analyze both the conventional flash smelting process and the newly developed Looping Sulfide Oxidation™ process, comparing heat and material balance results. LSO™ yields improvements to the energy footprint for copper, opening the door to new copper processing opportunities."

Jan 1, 2013

By Bart Blanpain, Muxing Guo, Zhuangzhuang Liu

In order to stabilize free lime in the basic oxygen furnace (BOF) slag to achieve high value products, quartz sand and other additives are injected into slag. However, the current hot stage slag stabilization does not work in case of slag (before treatment) with a liquid fraction lower than 90%, where the slag containing solid particles is too viscous. Therefore, it is essential to understand how solid phases affect the viscosity of the slag system. In this study, the industrial BOF slags were investigated with respect to the correlation between volume fraction of solid phases and its viscosity. Slag viscosity was measured with a rotating type viscometer at temperatures below the liquidus. The volume fraction of solid phases was quantitatively calculated with FactSage. The Einstein-Roscoe equation was employed to predict the viscosity of BOF slag.

Jan 1, 2016

By M. S. Moats

The treatment of oxidized residues of zinc with high iron content continues to present a technical challenge in both the steel and zinc industries. Two main problems are commonly identified and include high treatment costs and environmental concerns about contaminated, iron-bearing residuals. A new approach to this problem is described in which selective separation of the iron and zinc into salable products may be potentially feasible. The waste material is first leached to give a solution having an approximate concentration of 110 g/l Zn, 15 g/1 Fe and 40 g/1 H2SO4 and other impurities such as Pb, Cd, Cu and Sb. A suitable organic, such as D2EHPA, is used to load the majority of the iron. The aqueous phase is then acceptable for zinc electrowinning after standard solution purification. The novel step in the flow sheet is the efficient recovery of the ferric iron from the organic solvent using a solid metal to reduce the iron to the ferrous state. The Fe+2 is easily stripped into an aqueous phase in a relatively pure form, suitable for use in water treatment. Process parameters and possible flow sheet designs are described and discussed.

Jan 1, 1995

By Bruce W. Wessels

"Metal-organic chemical vapor deposition has been shown to be a highly versatile technique for the synthesis of complex oxides. High dielectric constant oxide thin films of SrTiO3, BaTiO3, Ba1-xSrxTiO3 and SrxBa1-xNb2O6 can be be be deposited at 800 ºC with this technique. The fluorine substituted B-diketonate precursors have been shown to be well-suited for the deposition of high quality, epitaxial thin films of these materials.IntroductionThere has been a resurgence of interest in thin film ferroelectric oxides as a result of the development of techniques to deposit high quality material. Both physical and chemical vapor deposition techniques have been realized. Of the chemical vapor deposition techniques, metal-organic chemical vapor deposition (MOCVD) has received the most interest for the deposition of ferroelectric oxide thin films. This results, in part, from the availability of a number of volatile metal-organic precursors.(l) Moreover, MOCVD offers the advantages of high growth rates, uniform coverage over large areas, conformability, abrupt interfaces and excellent epitaxial crystallinity. Of the metalorganic precursors, the B-diketonate complexes have played an important role especially in the deposition of ferroelectric oxides containing alkaline-earth metals such as BaTi03 and Ba1•XSrxTi03. For example, barium tetramethylheptanedionate Ba(thd)2 has been used in the preparation of BaTi03 by MOCVD.(2) These compounds, however, are not without their problems. Ba(dpm)2 has a relatively low volatility; and as a consequence, temperatures in excess of 180·C are required for volatilization. This leads to the necessity of a complex precursor delivery system to insure that the precursor does not condense before the reaction zone. Moreover, the Ba precursor tends to oligomerize leading to a decrease in vapor pressure as well as a problem with reproducibility. To counter these problems, novel liquid source and solid source precursor delivery systems have been developed. (3)(4)"

Jan 1, 1994

By K. Adham

For use in many existing and emerging applications, the purification of natural graphite is required to achieve +99.9% carbon content with minimum metallic impurities. Currently, the hydrofluoric acid process is used, which carries certain environmental and workplace health and safety impacts. While thermal purification of graphite at temperatures over 2500 °C is a known alternative, such high-temperature furnaces are expensive to build and operate. Using chlorine at lower temperatures to purify graphite is also known and patented, but is currently limited to treating solid synthetic graphite shapes in small-scale batch furnaces. Chlorine treatment of natural flake graphite resources can be used commercially, if certain drawbacks are addressed through process improvements that can be helped with the use of fluidized bed reactor technology.

By Ho Jung Heo

The proper control of slag composition is a dominant factor affecting yield of iron as well as dephosphorization efficiency in an electric arc furnace (EAF) operation. Moreover, thermophysical properties of slags such as viscosity are strongly affected by the changes in slag composition. Slag foaming, which is also a function of viscosity, is directly connected with the yield of iron and thus optimum slag chemistry are highly required in view of thermodynamics and physical properties. Therefore, we analyzed the slag composition in commercial melt shop (70 ton EAF) with the aim of higher yield of iron as well as higher dephosphorization during EAF process.

By S. N. Monteiro, C. M. F. Vieira, A. P. N. M. de Sa, J. P. D. Vitorino

"This work has as its objective to characterize an ash waste and to evaluate its incorporation into a clay to produce bricks and roofing tiles. The waste is a type of fly-ash resulting from the incineration of a selected part of urban garbage, which is basically constituted of organic matter and plastics. The waste was submitted to mineralogical and chemical characterization. Compositions were prepared with incorporation of the waste in amounts of up to 20wt.% into athe clay. Rectangular specimens were prepared by extrusion and fired in a laboratory furnace at 900°C. The physical and mechanical properties evaluated were: linear shrinkage, water absorption and flexural rupture strength. The results showed that the waste is predominantly composed of quartz and calcium compounds. The incorporation of the ash was deleterious to the evaluated properties of the clay. It is suggested that the incorporation should be made in amounts below 5wt. % to avoid deleterious effect in the mechanical strength and water absorption of the clayey ceramic.IntroductionThe world attention has turned to a subject of great concern today, the production and disposal of large amounts of industrial wastes as well as wastes of various sources. When deposed in an unsuitable place, these wastes can cause considerable harm to human health and to the environment. Our planet suffers with air pollution, groundwater and soil contamination as well as silting of rivers and lakes with the growing amounts of our society wastes.The recycling of waste materials is of great interest to the industries, mainly due to the environmental agencies legislation. One of the practices for correct disposal of these wastes being investigated is to incorporate into red ceramics, such as bricks and roofing tiles. The natural variability of the characteristics of the clays associated with the relatively simple processing techniques and also the low performance required for the products allow the presence of relatively high levels of impurities in clayey ceramics."

Jan 1, 2011

By Yuanpei LAN, Minren XU, Deliang NIU, Zhu WANG, Qingcai Liu, Shan Ren

Removal of gas is the major function of RH degasser. To optimize the RH refining craft in Chongqing Iron and Steel Co. Ltd, the degassing effect of RH degasser at different degrees of vacuum was investigated using a vacuum induction furnace. In addition, the effect of processing time on the gas content dissolved in molten steel was also studied. The results showed that degree of vacuum was one of the important factors that determined the degassing efficiency in RH refining process. High vacuum degree is helpful in the removal of gas, especially in the removal of [H] dissolved in molten steel. The processing time could be reduced from 25-30 min to 15 minutes and gas content could also meet the demand of RH refining

Jan 1, 2015

By B. C. Curson

A comprehensive simulation of .the gas handling system in BHP Copper&apos;s San Manuel smelter was developed using AFT Fathom software, with the objective of minimizing SO2 emissions while maximizing smelter throughput. Once verified with plant data, the simulation quickly revealed&apos; the complex interactions occurring between individual converters and the flash furnace. The increased understanding provided by the simulation allowed novel, counter-intuitive control strategies to be developed and tested successfully.

Jan 1, 1999

By A. G. Raraz

Reactive metal electrorefining presents a number of problems that pose obstacles to commercial operation. Cerium has been chosen as the surrogate for certain reactive metals because of its thermodynamic and electrochemical characteristics. A comparative review of the properties for cerium and plutonium has been presented to justify the choice of cerium as the surrogate metal for studying electrorefining. This review has addressed the electrochemical, thermodynamic, and kinetic parameters of molten salt electrorefining of cerium metal to provide an insight to this extremely important process. The cell components and configuration, current efficiency of the process, purity of the cathodically deposited metal and the power requirement of the system are evaluated for a molten CaCl2-MgCl2 salt electrolyte using a molten, stirred impure anode. Crucible designs, salt electrolyte, cell temperature and electrode materials are also evaluated. Selection of the salt electrolyte and the cell temperature have been suggested from this study.

Jan 1, 1992

By Dewei Zhu

A general purpose computer model for describing the transport phenomena and resulting rate of deposition in Chemical Vapor Deposition (CVD) processes has been described. Partial differential equations describing the conservation of mass, momentum, energy and chemical species are solved by a computer program employing a finite volume method. The program allows for multiple chemical species and natural convection effects. In this paper, the deposition of silicon by the reaction of silicon tetrachloride and hydrogen in a vertical stagnation flow reactor with rotating substrate has been considered. The effects of reactor pressure and substrate rotation speed on the rate and uniformity of deposition have been studied. The predicted rates of silicon deposition along the substrate are in reasonable agreement with experimental results found in literature. The model can be used as a tool for design optimization of such reactors.

Jan 1, 1990

By Pengfu Tan

Electric arc furnace (EAF) dust from the steel industries is listed by the United Sates EPA as a hazardous waste under the regulations of the Resource Conservation and Recovery Act due to the presence of lead, cadmium and chromium. The disposal of the approximately 650,000 tons of EAF dust per year in the U.S. and Canada is an expensive and unresolved problem for the majority of steel companies. The Waelz process has been considered as the best process for treating EAF dust. A process model, combined thermodynamic modeling with heat transfer calculations, has been developed to simulate the chemical reactions, mass and heat transfer and heat balance in the kiln. The injection of air into the slag and the temperature profile along the kiln has been modeled. The effect of (CaO+MgO)/SiO2 on the solidus temperature of slag has been modeled also and discussed. Some optimizing results have been presented in this paper.

Jan 1, 2005

By Xiao Y. Yan

A fused salt electrochemical process was investigated for the synthesis of non-oxide ceramic powders directly from metal oxides, boric oxide, and carbon powders by electro-deoxidation. Sintered pellets of the mixed powders were designed to act as a composite cathode in the electrolytic cell. Electrolysis was carried out in molten CaCl2-NaCl eutectic at 3.1 V and at 600-900 ºC under argon. The favoured cathodic reaction was the removal of the oxygen from the oxides to produce metal atoms that reacted with either the reduced boron atoms, forming a metal boride, or the carbon initially present in the sintered pellets to produce a metal carbide. The technical viability of the process was demonstrated by the electro-deoxidation of sintered pellets of TiO2/B2O3 and TiO2/C to produce TiB2 and TiC, respectively. Compared to existing carbothermic reduction process, this new electrochemical process may be less energy intensive and may lead to lower production costs. I

Jan 1, 2008

By Jonkion M. Font

Due to the known disadvantages of the use of iron silicate slag in the nickel converting stage, i.e., high metal losses, high magnetite content, and low fixation of impurities in the slag, the development of the new proposed "ferrous calcium silicate slag" for smelting and converting processes of nickel is very promising. Hence, considering the successful experimental results of using CaO base slag for the nickel smelting process, a study based on a detailed comparison for the phase equilibrium, and the minor elements distribution between the Ni3S2-FeS matte with either FeOx-CaO or FeOX-Si02 base slag was investigated. The main results are summarized as: no difference in the nickel losses between both slags was found at high nickel content in the matte, and the fractional distribution analysis for arsenic and antimony pointed out their preferential fixation in the calcium ferrite slag rather than in the iron silicate slag. Considering the energy and pollution issues, the technical feasibility of using calcium ferrite slag in a converting process of the Bessemer matte will have a prominent future for the nickel industry.

Jan 1, 2003

By Jose M. Gomez-Vega, Osamu Takai, Atsushi Hozumi, Hiroyuki Sugimura

"Ongoing research is reported aimed at improving the properties of mesoporous silica-based coatings on various substrates for optoelectronic or medical applications. Tetraethylorthosilicate (TEOS) was selected as the silica precursor, and amphiphilic triblock copolymers poly( ethylene oxide)- poly(propylene oxide)poly( ethylene oxide) as the surfactant micellar template or structure-directing agents. Cetyltrimethylammonium chloride (CTAC) was also used as a control agent. The effect of the templating agent and type of substrate (glass, Si, and Ti) on the mesoporosity, particularly on the alignment of the mesochannels, has been investigated. Three · different treatments (thermocalcination, photocalcination, and solvent extraction) have been also studied to remove the organic templates.IntroductionThe fabrication of mesoporous silicate-based materials through the utilization of a sol-gel process, where cooperative organization of organic and inorganic species takes place, provides a versatile approach to nanoscaled structures with potential applications in fields such as catalysts, optoelectronics, biomaterials, etc. Compared to conventional low molecular weight surfactants, self assembly of amphiphilic·block copolymers can result in mesostructured materials with larger pore sizes (up to 30 nm).1 Most of the synthetic strategies use silicon alkoxides as the silica precursor, although non-silicate metal alkoxides, e.g; Ti, Zr, Al, and B, have been also used to obtain different mesoporous materials, or even mixed metallic oxide systems. 2 Recently, Yang et al. 3 • 4 were able to synthesii:e a great variety of mesoporous metal oxides ID nonaqueous media using inorganic precursors (metal chlorides) and block copolymers as structure-directing agents."

Jan 1, 2000

By Robert D. Pehlke

"The evolution of oxygen steelmaking is reviewed and new operating processes are described. The developments which could impact this technology are summarized. Staged and continuous steelmaking are considered in the light of new technologies. The future opportunities for oxygen steelmaking processes are overviewed. IntroductionThe use of oxygen in steelmaking was originally brought on the scene by the development of pneumatic steelmaking. Sir Henry Bessemer in England originally conceptualized the use of gaseous oxygen in steelmaking, and then he and William Kelly in Eddyville, Kentucky independently developed the original pneumatic process which involved blowing air through a bath of molten pig iron to oxidize the carbon and silicon and produce steel. This process and many following processes, including those which would use pure oxygen gas, have been proposed.Beginning with the first commercial oxygen steelmaking vessels at Linz, Austria in 1952, the world steelmaking industry has adopted this style of processing. In general, the process has involved the use of steel scrap in amounts from 20 to 35% of the metallic charge with molten pig iron produced in blast furnaces making up the remainder. The impurities in the charge are oxidized through the use of oxygen gas injected into the steelmaking vessel.However, currently being adopted into commerical practice and on the horizon are a number of advances in this process which include the use of iron ores as a source of iron and oxygen, the use of an all scrap charge, incorporation of pre-reduced iron, the use of auxillary fuels to change the balance of cold and liquid iron-base charge materials and numerous refining techniques."

Jan 1, 1988

By Junwei Han, Wenqing Qin, Dawei Wang, Fen Jiao, Wei Liu

The removal of iron impurity from zinc calcine was studied by magnetization roasting and magnetic separation. The effects of roasting temperature, magnetic intensity, ore grinding, and leaching pretreatment on iron grade and recovery were investigated. The results indicated that iron recovery increased with the increase of roasting temperature or magnetic intensity, while iron grade was always less than 22%, depending on the fact that the magnetite were not liberated completely. The good liberation was difficult to be achieved by ore grinding but was easier by acid leaching, since the magnetite grains were very fine. After the leaching pretreatment, the recovery of 76.31% with iron grade of 53.24% was obtained by one roughing and cleaning. The SEM/EDS analysis showed that a part of sphalerite, zinc ferrite and other gangues were mixed into the iron concentrate, while some of fine magnetite was reported to the tailing.

Jan 1, 2016