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By Etsuro Shibata

The saturated solubility of chromium oxide and the valence of chromium in the slag are important matters when considering how to effectively utilize chromium-containing slags. The experimental data of various types of slags cited in the literature were arranged according to the optical basicity in order to evaluate the effects of the oxygen potential and the slag composition. The saturated solubility of chromium oxide and the Cr2+/ Cr3+ ratio tend to decrease with the increase of the optical basicity of the slag at an oxygen potential below 10.5 atm. However, at an oxygen potential of 0.21 atm, the saturated solubility and the Cr6+/Cr3+ ratio tend to increase with an increase of the optical basicity. A practical approach was suggested to reduce chromium in the stainless steel slag and simultaneously recover it as a ferroalloy by the direct smelting reduction of chromium oxide in the molten slag using some reductant in a small furnace.

Jan 1, 2003

By T. J. White

Each year, thousands of tons of toxic concentrates are produced as the unwanted byproducts of industrial operations and smelting activities. The fate of these materials remains open, as in general their consumption is limited and potential markets contracting. Xtaltite (pronounced crystal-tight) is a Synthetic Mineral Immobilization Technology (SMITE) optimized for the concentration, detoxification and consolidation of toxic metal wastes. In this approach, we seek to mimic nature to produce durable synthetic minerals that survive for aeons in well characterized geological settings. This approach has high public acceptability because the concept is easily understood by the layperson and the long term stability of the waste form may be predicted with confidence. In addition, where Xtaltite is used for mine backfill, a system of ecologically sustainable mining development is established. This paper details the design and fabrication of Xtaltite under oxidizing and reducing conditions. To illustrate and contrast these stabilization regimes, specific reference will be made to the treatment of thallium, chrom~um and arsenic wastes. Waste form performance under TCLP, dynamic boiling water tests and in other leaching media will be compared and discussed with respect to their relevance to different disposal options.

Jan 1, 1995

By Howard K. Worner

"In a rewarding career spanning nearly two thirds of a century, the author has worked at the frontier of such diverse fields as the creep of metals, structure properties and production of novel dental and surgical materials, molten salt electrolysis for titanium production, greatly improving the productivity of large iron blast furnaces and of oxygen steelmaking. While each of these has given great satisfaction, special thrills have derived from the development of new methods for the continuous production or refining of both ferrous and non ferrous metals. A rewarding segment was the evolution of various aspects of WORCRA technology. Unfortunately, several of these inventions have been ""ahead of their time"". Introduction""I am greatly honoured by the convening of this meeting to recognise my contributions to pyrometallurgy. My appreciation is the greater because this is the third Howard Worner Symposium; the first took place in the University of Newcastle in 1988, close to my 75th birthday. It was arranged by the local branch of The Australasian Institute of Mining and Metallurgy with the theme, ""Frontiers in Pyrometallurgy"". The second was organised by the University of Wollongong in conjunction with the Australian Academy of Science and the Australian Academy of Technological Sciences and Engineering; it celebrated my 80th birthday and, at my request, covered a broad range of topics under the heading of ""Recent Advances in Science and Technology"". Now, this very international meeting on ""Injection in Pyrometallurgy"" has been convened by the G K Williams Co-operative Research Centre for Extractive Metallurgy in my alma mater. I am both delighted and honoured that the cosponsors are the TMS (USA) and ISIJ (Japan).Dr Madhu Nilmani consulted me about the field to be covered and I readily concurred because ""injection"" has been of keen interest to me since the beginning of the 1960s when I began my pioneering work on sequential oxygen (or air) injection into flowing streams for both refining of blast furnace hot metal to steel and for the continuous smelting-converting of copper and nickel."

Jan 1, 1996

By Ken-ichiro Uemura

"The DIOS process has been developed for eight years since 1988. The research project was started with the element studies carried out by each of the five integrated steel making companies in Japan, the final two and half years were spent for the pilot plant studies. Operation were conducted in the entirely closed and pressurized system successfully as planned. From the result, the DIOS process was proved to be viable as a future iron-making process substitutable for the conventional blast furnace. In addition, a lot of findings were obtained. Hot metal productivity was primarily determined by a oxygen flow rate, and a coal consumption varied depending on the productivity. The post combustion ratio was a little lower than expected from the result of the element study. It was supposed to relate the gas-reforming with coal or volatile matter in the free space of the furnace. Hot metal carbon content seemed to depend on the char content in slag.INTRODUCTIONThe JISF's DIOS pilot plant (DIOS=Direct Iron Ore Smelting Reduction Process) has finished its last campaign of the operations in January 1996. The project was started in 1988 as a joint research of the Center for Coal Utilization, Japan and the Japan Iron and Steel Federation (JISF) with a subsidy for promoting coal productions and utilization technologies from the Agency of National Resources and Energy, the Ministry of International Trade and Industry(MITI). Throughout the pilot plant test, a total of over 20,000 tons of hot metal was produced for more than 2,000 hours of the operation. Recorded production rate was 538 ton/day for 3 days at a specific coal consumption of approx. 1,000kg/hmt. Long-term operation was carried out in the fifth campaign for 18 days, which has proved that the entirely closed and pressurized DIOS process works well as planned. In Figure 1 is shown the representative operational performance obtained in the first five campaigns. The project is going to be finished by the end of March this year after investigating the technical viability and economic potential of the process, and completing the conceptual design of the DIOS commercial plant. In this paper, the system and facilities of the DIOS process are first introduced and some of the results of the pilot plant test are detailed later."

Jan 1, 1996

A novel process is being developed for metal recovery from waste electrical and electronic equipment involving a leach reactor coupled to an electrochemical reactor. Metals such as Ag, Au, Cu, Pb, Pd, Sn etc. are dissolved from shredded electronic scrap in an acidic aqueous chloride electrolyte by oxidising them with aqueous dissolved chlorine species. In the electrochemical reactor: (i) chlorine is generated at the anode for use as the oxidant in the leach reactor, and, simultaneously, (ii) at the cathode, the dissolved metals are electrodeposited from the leach solution. The extended Butler-Volmer equation was used to provide predictions of the electrode potential dependences of partial current densities and, hence, total current densities, current efficiencies and alloy compositions for acidic aqueous chloride electrolytes containing Ag(I), Au(III), Cu(II), Pb(II), Pd(IV) and Sn(IV) species, together with dissolved chlorine. With judicious choice of kinetic parameters, the predicted total current density ? electrode potential behaviour of such solutions was in good agreement with experimental data for a rotating Pt disc electrode. Reduction of dissolved chlorine at a Pt rotating disc electrode exhibited mass transport controlled behaviour, in agreement with Levich?s equation over the potential range 0.3-0.9 V (SHE). This could form the basis of a linear sensor, possibly using a microelectrode for measurement and control of the dissolved chlorine concentration in the efflux of leach reactors and inlet to electrowinning reactors in the envisaged process.

Jan 1, 2003

By Veneta Groudeva

A pyritic ore containing zinc, lead and copper as? the relevant primary sulfide minerals, .as well as gold and silver finely disseminated in the sulfide matrix, was? leached in percolation columns. Each column contained 30 kg of ore crushed to minus 10 mm. Firstly, zinc and copper were efficiently leached by means of chemolithothrophic bacteria? in acidic sulfate bearing medium. Zinc was leached more rapidly than copper but the final extractions of these metals were similar (about 75% in 300 days). A part of the galena was oxidized to the. insoluble lead sulfate during the leaching. The pyr:ite was, however, relatively slightly attacked. The ore was then leached by means of FeC11 - HCl solutions both in the presence and in the absence of bacteria to solubilize the lead. The chemolithotrophic bacteria grew in media containing both chloride and sulfat~ ions and maintained a high ferric to ferrous ion ratio in the percoiating solutions. The chemical leaching was, however, more efficient since ft was possible to carry it out at higher chloride ion concentrations. About 10% of the lead was leached in this way in 90 days. Finally, the ore was leached by thiourea in the presence of a gold-oxidant (oxone) to extract the gold and silver. Over 60% of the gold and over 55% of the silver were extracted from the ore in 150 days, while. the extractions of these precious metals from an untreated ore sample were lower than 25%.

Jan 1, 1991

By R. S. Celmer

The distributions of cobalt, molybdenum, copper, and selenium between nickel matte and silica-saturated iron silicate slag have been determined in the region of the metallic saturation boundary, at 1523 K. Results are given as a function of the composition of the coexisting Fe-Ni alloy and the activity of iron in the system. Under strongly reducing conditions, these minor elements display a marked preferential accumulation in the sulphide phase. It is shown that the dissolution of cobalt and molybdenum in slag follows an oxidative mechanism, and distribution equilibria are correlated with the oxygen potential. From these data, the thermodynamic properties of cobalt in nickel matte are computed. Further, comparisons of minor element partitions are made between the nickel and copper matte smelting cases under metal saturation conditions.

Jan 1, 1988

By George S. Dulikravich

An advanced semi-stochastic algorithm for constrained multi-objective optimization has been adapted and combined with experimental testing and verification to determine optimum concentrations of aJ10ying elements in heat-resistant and corrosion-resistant H-Series austenitic stainless steel alloys. The objective was to simultaneously maximize a number of alloy's mechanical properties. This research will result in a rigorous tool for the design of high-strength H-Series steels and other types of alloys unattainable by any means existing at the present time. Such a material-by-design tool will also be able to reduce or minimize the need for the addition of expensive elements such as Cr, Ni, Co, Nb, Ti, V, etc. and still obtain the optimum properties of an aJ1oy.

Jan 1, 2003

By Oleksandr Liaskovskiy, Sergey Beringov, Sergiy Yatsuk, Timur Vlasenko, Iryna Buchovska

"Working with solar-grade silicon for solar cells application usually meets some difficulties in comparison to polysilicon produced by Siemens method: higher impurities content leads to lower yield, worse electro-physical parameters and poor performance in solar cells application. However some adjustments in ingot production can show significant improvements in quality of final product: crystalline wafers and cells.Recent investigations have shown that solar-grade silicon is suitable for high effective production process such as mono-like multicrystalline wafer production. Production-scale lots made at Pillar show promising results for solar-grade silicon application: high-quality wafers with significantly big crystalline grains of <100> orientation.IntroductionThe standard technology of producing multicrystalline silicon ingots by directional solidification method in quartz crucibles has a number of disadvantages resulting in limited efficiency of solar cells made of multicrystalline material: crystallites of multicrystalline ingot are relatively small (down to 5 mm size), grain borders of crystallites contain parasitic impurities such as metals, silicon nitride etc., crystallographic orientation of crystallites is random. The listed deficiencies are an integral characteristic of the technology which affects the efficiency of solar cells, such as presence of solar cells with low efficiency even at a high level of average efficiency, problems with shunted cells, silicon nitride inclusions, which adversely affect cell efficiency and are centres for silicon carbide formation, impossibility of application of high effective alkaline texturing etc. Also with regard to the targets set by photovoltaic to reduce the cost per Wp in the nearest future, standard technology of multicrystalline silicon ingots production by directional solidification faces certain challenges some of which are hard to overcome due to rather low efficiency of solar cells made of multicrystalline wafers. Therefore alternative methods of multicrystalline silicon production for photovoltaic application having a number of advantages in comparison to traditional technology are developing rapidly."

Jan 1, 2012

By Mei-le He, Min Chen, Xiang Shen, Lei Xu, Lei Liu, Nan Wang, Xue-liang Yin

In the current study, Al2O3-MgO-CaO refractories were prepared at 1400-1600 by the addition of MnO micro-powders, and the effect of MnO addition on densification behavior of the refractory was discussed. The results showed that the doped MnO dissolved to MgAl2O4 phase, and promoted the growth of MgAl2O4 grains by the formation of MgAl2O4 solid solution. As a result, the dense microstructure was obtained, with the apparent porosity decreased from 19.2% to 5.4% and the bulk density increased from 2.78g/cm3 to 3.15g/cm3 after firing at 1600 for 2h by the addition of 4% MnO. In addition, a texture microstructure was observed, which is considered to be favorable to improve mechanical properties and the service life of Al2O3-MgO-CaO system refractories.

Jan 1, 2016

By Masayasu Kawahara

"The extraction and separation of nickel, cobalt and copper were investigated with a solvent impregnated resin which was produced from UX84-I and XAD-4. The extraction behavior of metals with the solvent impregnated resin is similar to that with solvent extraction. The extraction ability of solvent impregnated resin improves when using finer particle resin and with a higher concentration of extraction solvent.IntroductionSolvent extraction is well known-as a method for separation of metallic elements in solution. However there are problems with intermediate phase and solvent loss. Ion exchange resin is also used in hydrometallurgy, but it is not fit for separating a large quantity of metals. Amberlite XAD-4 resin is known as a absorption agent of organic matter in water. It is expected that the resin which has the ability of extracting metals can be made by absorbing organic extractant on XAD-4 resin In this study, solvent impregnated resin (SIR) was produced from LIX84-I and XAD-4, and extraction and separation of nickel, cobalt and copper were conducted using SIR. The extraction properties of SIR were investigated, and a comparison between ordinary solvent extraction and SIR was made.Experimental ProcedureAmberlite XAD-4 was used as absorption resin for the organic extractant in this study. The physical properties of XAD-4 are shown in Table I. Amber lite XAD-4 has a large surface area and shows good ability to absorb organic matter in water, but the: resin does not have the ability of exchanging metallic ion."

Jan 1, 2000

By Liping Gu, Gordon A. Irons

"A 1/3 scale ""thin-slice"" model of an electric arc furnace was developed so that gas could be injected to simulate foaming gas evolution. The influence of arc jets, oxygen lancing and bottom bubbling was also simulated. Liquid velocities were measured by a white light particle image velocimetry system. Numerical simulations of some of these effects were made using commercial CFD packages. Comparisons with measured results show that considerable care is required to select the appropriate model and to interpret the computational results.INTRODUCTIONDuring recent years electric arc furnaces (EAF) have captured a significant share of steel production, partially due to increased productivity through the introduction of advanced technology such as oxygen injection, slag foaming and long-arc operation, process automation and post-combustion. However, systematic analysis of the process and these effects on heat transfer and fluid flow in the furnace is still in its infancy. Most investigationsl1 6l have been restricted to a specific application such as oxygen lancing or bottom stirring. In addition, it is very difficult to make comparisons between these computed results and experimental/industrial results. In this work a 1/3-scale ""thin-slice"" model of Dofasco's 190 ton EAF was built. The fluid flow in the bath due to the arc jets, bottom stirring, oxygen lancing and CO evolution was simulated. The velocity distributions in the bath were measured using Particle Image Velocimetry (PIV) System. In addition, numerical simulations of bottom stirring and CO evolution were carried out using two commercial CFD packages (Fluent and Phoenics). The objective of this work is to validate the mathematical models so that they can be applied to the full-scale furnaces."

Jan 1, 1999

By T. T. Chen

Gold in the Twin Creeks ore is primarily associated with arsenian pyrite. During pressure oxidation, the sulphides are solubilized, but part of the dissolved iron reprecipitates as jarosite and as an iron sulphate-arsenate-phosphate phase. The pressure oxidation products are subjected to cyanide leaching. The cyanide leach residues consist of quartz, gypsum, bassanite, anhydrite, small amounts of jarosite, an iron-sulphate-arsenate-phosphate phase, as well as trace amounts of orthoclase, rutile, pyrite, hematite and monazite; all these particles are dispersed in a fine grained matrix of illite-muscovite. The autoclave leach residues contain a small amount of carbonaceous matter. Many gold grains are detected on the surfaces of the carbon particles, and these gold particles are not leached during cyanidation. The gold particles are typically 0.1-0.2/Lm in size and commonly are embedded in the carbon surface or are coated with a K-AI-Si-S-O phase on the surface of the carbon. The gold grains are consistently associated with elevated CI contents (50-300 ppm Cl). The poor gold cyanide leach recoveries, which initially occurred in the Twin Creek developmental circuit under certain operating conditions, are attributed to the presence of chloride in the feed. This results in the formation of soluble gold chlorocomplexes in the autolcave and the subsequent sequestering of the gold on the surfaces of the carbon particles.

Jan 1, 2000

By Zhitong Sui

Based on several case studies on the precipitating behavior of valuable nonferrous metal compounds (VNMC) in molten slags a green technology for the recovery of VNMC from molten slags was proposed. This technology involves three steps: (I) The selective enrichment of the dispersed VNMC into the designed mineral phase in the molten slag; (2) The selective coarsening of the designed mineral phase to a critical grain size in the molten slag; (3) The selective separation from tailing of the grown mineral phase in the solidified slag by dressing or hydrometallurgy processes. This is a clean and low cost technique and has a great capacity to deal with a large quantity of slags. The utilization of the recovered VNMC such as Titanium, Boron, Vanadium compounds was summarized as examples of application. It was confirmed by experiments that the precipitating behavior of the designed mineral phases like Perovskite(CaTiO3), Suanite(2MgO*B2O3) and Sincosite(CaOoV2O5*P2O5) in molten slags is obviously affected by operation factors such as temperature, chemical composition, heat-treatment, additives and so on. The precipitating kinetics and mechanism of the VNMC from molten slags during solidification processes were also investigated.

Jan 1, 2003

By Nieves Iglesias

The removal of the refractoriness of a gold bearing pyrite- arsenopyrite ore is studied. Flotation concentrates were prepared and leached with a dilute acidic ferric sulfate solution. The elemental sulfur film which forms on arsenopyrite in the oxidation process is not responsible for the low rate of the arsenic dissolution observed. A positive effect on the leaching rate is observed when Ag&apos; is added. This pretreatment eliminates the refractory nature of concentrates.

Jan 1, 1993

By Hong Yong Sohn, Miguel Olivas-Martinez

"Different approaches are used for calculating the ‘energy requirement’ of a process. The determination of energy requirement becomes confusing for a process in which a fuel is also a reactant. The key issue is which heat of chemical reaction should be included in the ‘energy requirement’ value. We will use the example of ironmaking processes to illustrate the problem. The different approaches essentially boil down to the question: does one include the combustion heat of the reductant used in the reduction reaction or just the heat of the reduction reaction? Depending on the viewpoint, either approach can be accepted; it is a matter of convention. There is a need, however, to select a standard approach because the absolute value of ‘energy requirement’ of a process depends on the choice. The energy requirement of a novel flash ironmaking process will be compared with that of an average blast furnace operation.IntroductionDifferent approaches are used for performing energy balance calculations and perhaps more significantly in presenting the ‘energy requirement’ of a process. The question becomes more involved for a process in which one or more reactants are also used to generate the process heat by combustion. Often the key issue is which heat of chemical reaction to include in presenting the ‘energy requirement’ of the process.It is worthwhile to note at the outset that the difference in energy requirements between different processes for converting similar raw materials to the same desired product is largely unaffected by the choice of chemical reactions to be included. However, the absolute value presented as the ‘energy requirement’ of a process can be different by a large amount depending on the approach. We use the example of ironmaking processes to illustrate the problem. In these processes, as currently practiced or under development, carbon and/or hydrocarbons (including hydrogen) are used as the fuel as well as the reactant for reducing the iron oxide mineral.The different approaches in this case essentially boil down to the following question: does one include the combustion heat of the reductant used in the reduction reaction or treat the reductant portion as just a reactant? Depending on the viewpoint, either approach can be considered acceptable. It is a matter of convention. There is a need, however, to select a standard approach because the absolute value of ‘energy requirement’ of an ironmaking process (e.g., the currently dominant blast furnace process) depends on such a choice. It is particularly important to clearly state the specific approach used when the energy requirement of ironmaking is compared with those of other industrial processes such as petrochemicals production."

Jan 1, 2014

By Gaballah I.

Elimination of arsenic, mercury and zinc from synthetic solutions containing H;\A.sD4. HgCI2 and ZnCI2 using modified barks was investigated. The pH range was varied from ?1 to 10. The initial concentrations of individual element were 10,100 and 1000 ppm. More than 99 % of mercury and 65 % of zinc cations were removed by the modified bark .. In this case, the modified bark reacts as a cation exchanger leading to the release of &apos; two protons for every HgII or ZnII fixed by this material. About 30 % of arsenic was eliminated from the solution. This &apos;low efficiency could be attributed to? the presence of arsenic ,as. anion. Decontamination of a treated industrial effluent containing 4 ppm of ion? metals was performed on a pilot plant scale by the modified bll(k. More than 70&apos;% of these ion metals were eliminated.

Jan 1, 1995

By J. Antrekowitsch

Keywords: residues, fluorides, chlorides, zinc, steel mill dust The recyclability of various nonferrous metal wastes often suffers from a relatively high fluorine and chlorine content. Both are inserted in most cases by the use of plastic contaminated scrap and a wide variety of different coatings. These halogens lead to poor product qualities and off gas contamination. Especially the history of zinc recovery from steel mill dusts shows, that the today common hydrometallurgical options are on their limit and therefore are not sufficient in most cases. This thermochemical study should give more information about different pyrometallurgical options, that offer both a chlorine and fluorine reduction and efficient zinc recovery, preferably in one process step. Selective evaporation in different atmospheres and conversion with the use of hydrogen are the main parts in this study. The results combined with the relatively small information available from literature should provide a basis for further investigations in this field.

Jan 1, 2005

By J. M. Rapkoch

In late October 1996, an acid plant at a major U.S. copper smelter was faced with unexpected and rapidly increasing pressure drop across the gas cooling tower in the acid plant, indicating a build-up on the packing. This threatened to halt operations if not resolved. Earlier that month, a smaller vessel in the acid plant was found to be completely plugged with lead sulfate. It was feared that a similar fate awaited the gas cooling tower unless the scale build-up was stopped. Although lead sulfate is present in most copper smelter acid plants, this accumulation was unusually severe. An investigation was launched to find the source of the lead, determine how lead is transported to the gas cooling tower, recommend operating practices to prevent such severe scaling, and seek ways to recycle the lead value in the scale covered polypropylene packing. Late in the investigation it was learned that the lead originated from an improperly executed recycling program.

Jan 1, 2000

By R. W. Bartlett

The extensive central Idaho black sand placer deposits are a potential source of rare earth elements, particularly the heavy rare earth elements that are not prevalent in commercial bastnasite deposits. These placers derive from the Idaho batholith. The geology, occurrence, and extent of these deposits are reviewed and the diverse mineral assemblages and complex mineral chemical compositions of these sands are described. Niobium, yttrium and thorium are also present in significant concentrations. The results of prior mining practice, including concentration and separation of the heavy minerals are reviewed. Technical approaches to extraction of rare earths from Idaho black sand concentrates are discussed.

Jan 1, 1992