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By Toyohisa Fujita

The effect of variables on the gold extraction with ammonium thiosulfate was investigated on sponge gold and ore samples. The Effects of CUS04, (NH4hS203, NH40H, (N~hS04' pH, stirring speed and retention on gold leaching rate and thiosulfate oxidation (consumption) have been studied. Almost 100% of gold was leached from sponge gold and over 96% from ore sample at optimum conditions. Trioctylmethyl ammonium chloride was used to recover gold from thiosulfate pregnant solution. It was found that more than 99% of gold was recovered by the extractant diluted with n-octane at 01 A ratio of 1: 1 without the re-adjustment of pH or others. Also, the gold cementation was conducted without de-aeration by using zinc, copper and aluminum powders. The result indicated that the gold was effectively recovered from a solution of low ammonia and copper concentrations and higher thiosulfate concentration. The gold recovery process by using ammonium thiosulfate is an environmental friendly method comparing to conventional cyanidation process.

Jan 1, 2003

By Laurence Whitty-Léveillé

Proper handling of the radioactive fraction associated with the production of rare earth elements (REEs) in the mining industry is essential for a sustainable environment and human health. Actinides, such as uranium and thorium, have similar chemical properties to REEs, and are often co-dissolved in current hydrometallurgical processes. This causes radioactive contamination of the infrastructure through the extraction cycle. The present study optimizes, through experimental design, a sequential leaching procedure with Na2CO3/NaHCO3 and HCl for the rapid and selective dissolution of REEs and actinides. Optimization focuses on the main operating parameters (time, temperature, and concentration); different types of minerals, REE composites, and ores; on achieving maximal leaching yield; and on minimizing dissolution of the gangue metals (Fe, Si, and Ca). The final sequential procedure was rapid (1 h), effective, and led to the segregation of Th, U, and REEs with limited dissolution of the gangue metals.

By J. R. Donald

Electric arc furnace (EAF) dust, which can be considered as a by-product of the steel recycling process, contains significant quantities of recoverable zinc and iron, as well as hazardous elements such as cadmium, lead and chromium, which can be leached by ground water. The zinc in the EAF dust is found almost entirely in the form of either zinc oxide or zinc ferrite, the latter accounting for 20 to 50 percent of the total zinc. It is important that an efficient process be developed which renders the dust inert, while reclaiming the valuable metals to off-set processing costs. During the conventional carbothermic reduction processes, iron is formed, and this iron can participate in the reduction of the zinc oxide in zinc ferrite. In the present work, the reduction of the zinc oxide in zinc ferrite by iron according to the following reaction: ZnO-Fe2O3(s,s) + 2 Fe(s) = Zn(g) + 4 FeO(s) was studied in an argon atmosphere using a thennogravimetric technique. First, a thermodynamic analysis was performed using the F*A*C*T computational system. Then, the effects of briquette aspect ratio (lid), temperature, zinc ferrite particle size, amount of iron added, as well as additions such as lime, sodium chloride, and calcium fluoride were investigated. It was found that, initially, the reaction was chemically controlled with an activation energy of 178.1 kJ/mol. Then, after a product layer had formed on the outer surface of the briquette, the reaction was restricted by the diffusion of zinc gas away from the reaction interface. The parabolic rate law was fitted to the experimental data, and the parabolic rate constant was found to be: = -6.2275 + 0.0054 T (K)

Jan 1, 1995

By Kenneth N. Han

Ammonia has been found to be an effective leaching reagent for gold, silver and platinum group metals in the presence of appropriate oxidants. Electrochemical and kinetic aspects of the dissolution of elemental gold in ammoniacal solutions have been investigated. The cathodic reaction of aurous di-ammine on the gold cathode has been investigated first. From this investigation, the standard electro-potential of the cathodic reaction .and hence. the Gibbs free energy of formation of the aurous di-ammine were established. The solubility of gold in ammoniacal solutions was also examined in relation to ammonia concentration, temperature and concentration of various oxidants. The anodic reaction of the gold disk in ammonia? in the presence? of various oxidants including oxygen, ozon, hypochlorite, hydrogen peroxide, cupric and cobaltic ammine, and iodine was also examined and the results have been discussed. Excellent dissolution yielding of gold and many other metals, typically better than 95% recovery in 1'-2 'hours of leaching at a temperature ranging 80°C to 190°C has been observed. Test results of the dissolution of gold from elemental state as well as other sources including sulfidic ores and scrap are presented.

Jan 1, 1998

By O. E. Omotoso

This study is part of an ongoing investigation to understand the mechanism of stabilization/solidification of hazardous chromium wastes in ordinary Portland cement (OPC). Tricalcium silicate (C3S*),a major component of OPC is mixed with reagent grade Cr(lll) and Cr(VI) solutions, to simulate complex cementiCr waste systems. Scanning electron microscopy (SEM) and energy disperse spectrometry (EDS) were employed to provide microstructural and chemical information. Transmission electron microscopy (TEMlEDS), apart from complimenting the SEM, was used to probe the distribution of Cr in the hydration products of C3S and to provide crystallographic information. 29Si MAS NMR (magic angle spinning - nuclear magnetic resonance) Was used to characterize the influence of Cr on the hydrated silicate structure.

Jan 1, 1995

By Selim Coskun

In this study, tungsten matrix composites reinforced with 2 wt% TiC particles were mechanically alloyed (MA?d) for 3h, 6h, 12h and 24h. 1 wt% Ni is used as sintering aid which is added before and after mechanical alloying. Microstructural and phase characterizations of composite powders and sintered samples were carried out via SEM and XRD analyses. Furthermore, density and hardness measurements of as-consolidated and sintered samples were carried out. Additionally, DSC experiments were conducted to investigate the sintering behavior of the MA?d powders.

Jan 1, 2009

By Yoshio Waseda, Tetsuya Uda, Tom H. Okabe

"Halide salt has been tested as a reductant for producing titanium powder directly from TiCl4. From the results of thermodynamic investigation for several rare earth chloride systems, DyCl2 was found to be used for the reduction of TiCl4 instead of the conventional metallic reductant. When TiCl4 was fed into molten salts containing DyCl2 at 1073K, titanium powder of several ten micron meters in diameter was obtained. In contrast to the sponge titanium produced by the conventional Kroll process, the present new process using a halidothermic reduction in a reactive molten salt appears to be suitable for producing metal powder. From the thermodynamic point of view, the resultant DyCl3 can be reduced to DyCl2 by magnesium. By utilizing the multivalent halide redox couple, some possible ways of titanium powder production directly from TiCl4 by magnesiothermic reduction are shown to be feasible. This can also be applied to the development of a new continuous titanium reduction process.1 IntroductionTitanium and its alloys show attractive mechanical properties such as strength-to-weight, rigidity-to-weight ratios and excellent corrosion resistance. Nevertheless, the application of titanium alloys is limited compared to other structural materials (e.g. steels, aluminum alloys) because of its high cost of production. Currently, almost all of titanium is produced by metallothermic reduction of TiCl4 by magnesium (Kroll process)[1] in an airtight metallic reactor. This process is batch type and labor intensive. Therefore, many attempts to develop new process for producing titanium are investigated so far."

Jan 1, 2000

By Roger C. Urquhart

Copper-nickel-sulphide ores mined in the Rustenburg district of South Africa are generally smelted in electric furnaces because of the high-temperature slag produced, the availability of cheap electric power, and the smaller pollution problems. Apart from melting, the functions of the electric furnace are to recover most of the matte content in the converter slag by physical and chemical interaction with the furnace bath and to provide adequate time for the optimum separation of matte and slag. Smooth, efficient operation will denend on fluid slags for settling, balanced by high resistivities to obtain adequate concentration and distribution of power by way of current heating. To obtain a greater understanding of the processes involved, an investigation was undertaken at Rustenburg Platinum Mines on the smelting of copper-nickel concentrates in a 19.5 MVA furnace with six in-line electrodes. The matte- and slag-tapping temperatures, slag temperatures, slag analyses, electrical data, and electrode position were measured. Radioactive tracers were introduced into the slag, and quantitative results relating to the flow pattern within the furnace were obtained. These studies were augmented by scaled laboratory investigations relating to the determination of cell constants and current distribution within the furnace. Instantaneous field and power distribution plots were determined by use of an on-line mini-computer. The applicability of these results to furnace operation is discussed.

Jan 1, 1976

By Niander A. Cerqueira, Afonso G. Azevedo, Mairyanne S. Souza, Victor B. Souza, Victor T. Bartolazzi, Igor W. D. C. Pereira, Rondinelli C. Ribeiro

The common glass machining process used in the market of Brazil’s civil construction generates tons of waste through the folder of that waste disposal out by the water used during machining. After drying the product is intended for landfill representing a great environmental liabilities since these deposited glass waste in the environment have a decomposition time greater than four thousand years due to its high chemical and mechanical resistance. Aiming to give a destination that addresses this waste disposal problem in the environment, much has been studied in an attempt to incorporate them into the mix cement to partially replace the sand. In this work it was decided to carry out specific studies using common traits comparing the stroke with sand with a dash with partial replacement of 30% of the sand for the glass machining residue was analyzed resistance compressive resulting in a potential good product.

Mar 1, 2017

By Tomoya Nihei, Hiroshi Hayashi

"A novel selenium removal process called Recycled Green rust/Ferrite Process is developed by MMC. In this process, a mixed Fe2+-Fe3+ hydroxide compound, green rust (GR), reduces selenate to elemental selenium, while GR is consequently oxidized to magnetite Fe3O4. Sequencing batch-mode experiment showed that the residual selenium concentration gradually decreased with the number of batch test increased. Stable selenium removal was achieved when the number of batch test exceed 15 times. Optimum selenium removal ratio reached 99.95% where initial Se concentration 2.1mg/L decreased to 0.001mg/L. Furthermore, the continuous feeding test carried out through a pilot-scale plant with a feeding capacity 600 L/hr. Approximately 860-hour-feeding test was carried out for the selenium-contaminated groundwater which had an averaged selenium concentration of 0.88 mg/L. Selenium concentration in the effluent from thickener maintained less than 0.01 mg/L (selenium removal rate of 99%) until a net operating time reached 800 hours.IntroductionJapan is one of the largest producers of selenium, and thus there are potential environmental impacts of selenium on soil and aquatic environments. The Mitsubishi Material Corporation (MMC) owns some real estate properties whose soil and groundwater was polluted by selenium and other heavy metals. These sites include former industrial plants: a smelter for nonferrous metal and a fabricating semiconductors and pigments. Selenium in aquatic environment commonly exists in four oxidation states, namely, VI, IV, 0 and -II. Selenate ion (SeO4 2-), the most oxidized form of selenium, and selenite ion (SeO3 2-) are highly soluble and mobile. Elemental selenium (Se0) is insoluble in water and therefore has much lower toxicity. Because selenium is carcinogenic and teratogenic at high concentration, the national effluent standard in Japan is fixed at 0.1 mg/L and the environmental standard at 0.01 mg/L. Although there are several selenium removal techniques, the most conventional process is coprecipitation with a ferric hydroxide because of its simplicity and low cost. It is known that selenite is adsorbed strongly on the surface of ferric hydroxide, but selenate is not. The low affinity of selenate on oxide mineral surfaces was demonstrated by the fact that selenate could be easily displaced by adding competing anions, particularly sulfate ion. Selenate removal from polluted water is one of the most difficult techniques, and more effective methods are desired. MMC developed a novel selenium removal process [1]. In this process, the concentrated slurry that contains Fe(II)-Fe(III) hydroxyl-salts known as Green Rusts (GRs) contributes to selenate removal. The main components of the iron precipitate in the reactor are GRs and their oxidation product, magnetite (Fe3O4)."

Jan 1, 2008

"The pyrometallurgical method of recycling car batteries suffers from a potential for air pollution violations, which prompts the desire for a viable hydrometallurgicaJ alternative. Several Processes have been proposed, including leach-electrowinning routes using HBF4 and/or HzSiF6 based electrolytes, along with anodes of PbO2 on inert substrates.A study has been carried out to evaluate the proposed systems, with the intention of demonstrating a six month life of an electrolyte-anode combination. The work, which focused on the use of HzSiF6, has indicated that there was no acceptable anode, and has lead to the development of a technique to produce smooth, glassy, adherent coatings on graphite, and to the development of an anode composed of a series of copper cored graphite rods.The paper will present results on leaching and electrowinning experiments, as well as the description of a flowsheet for a pilot plant that will be used to produce one tone per day of refined lead from spent battery paste."

Jan 1, 1997

By Ali Akbar Mottahedi

It is known for a long time that the reaction of oxygen with carbon, silicon, iron and many other elements is exothermic. The heat of released from these kind of reactions can decrease the time of fusion of iron and steel for metallurgical purposes in the electrical arc furnaces. By decreasing the time of fusion, we increase the rate of process and the amount of production. So, by blowing oxygen in to the furnace, we can reduce the consumption of electricity and save cost. There are many problems in the procedure of the oxygen blowing. In this project, the theoretical aspect of the oxygen blowing and its side effects into the arc electric furnaces are investigated. An oxygen blowing system into the arc electrical furnace of metallurgy department of Machine Sazi factory was also set up. This process reduced the consumption of electricity up to 22% and increases the rate of production, by reducing tap ? to ? tap time up to 15%. In this project; all oxygen blowing systems and its control were set up.

Jan 1, 2006

By Roberto Parra

The wear and corrosion phenomena in the furnace lining of the ferrous and non ferrous pyrometallurgical processes are complex problems where chemical, interfacial and mechanical phenomena are presents. The characteristics of the processes determine the conditions to which these materials are submitted, where the thermal conditions reached during the operation is one of the most important parameter. Assuming that all the degradation phenomena are thermal activated, the rate of the different steps of the wear mechanism will depend on the thermal field in the lining. In view to apply the independent physicochemical knowledge of degradation mechanisms to the analysis and design of furnace lining the methodology of the Nodal Wear Model (NWM) was done. It combines the mathematical modelling of the heat transfer in the lining with the physicochemical control equation for the wear-corrosion phenomena. The NWM has been applied to different examples: theoretical analysis, laboratory scale test and industrial applications. We present in this paper the theoretical background of the model and two examples of applications: the sole of an electric furnace and the earth of a blast furnace.

Jan 1, 2006

The increasing need for robust pyrometallurgical furnace construction is driven by two trends in the copper and other base metals smelting industry: ? the desire for increased production within a single furnace line by greatly increasing smelting intensities, which generates high heat fluxes to the crucible. walls, and ? the operational and economic imperatives of maintaining high percentage on- line times and long campaign lives between rebuilds. A key feature of furnaces capable of producing at high rates, while containing intense processes, is a strong, thermally robust wall cooling system. Equally important design aspects include the furnace steel structure, refractories, a cooling water supply and piping arrangment for safety from leaks and disruptions, and instrumentation/controls for monitoring and rapid mitigation of process excursions. Integration of the cooling elements into these furnace systems is essential for optimum performance of the cooling elements, and indeed the entire furnace. This paper discusses the development of a composite copper / refractory water- cooled design, which has been successfully implemented on several copper smelting and converting furnaces, including Kennecott's flash converting furnace, INCO's MK reactor, and Kidd Creek's converting furnace.

Jan 1, 1999

By P. Barrios

Over a period of one year, an in-depth investigation was carried out in a conventional copper refinery to understand the behaviour of silver in copper electrolysis. The increase in silver content in the cathodes increases almost linearly with the duration of electrolysis, and the silver content of the electrolyte between the electrodes shows similar behaviour. The silver content of the cathode deposited daily depends directly on the silver concentration of the electrolyte and this, in turn, is strongly influenced by its internal temperature. The average temperature between the electrodes rises from the first to the second and to the third crop, because of the increase in the distance between the electrodes and the heat generated by the passage of the current. The mechanism of dissolution of silver from the anode, and its passage to the cathode, are discussed. Following the change to the Isa system, it was proved that the results and conclusions are analogous. Based on these results, a reduction of more than 20% in silver losses in the cathodes was achieved.

Jan 1, 1999

By Khosrow Nikkhah

Increasingly ion exchange systems are being included in design of hydrometallurgical plants for metal extraction or impurity removal. Because such systems operate sequentially and are based on resins that exchange one ion for another, store it temporarily and release it to a regenerating solution, the usual steady state heat and mass balancing tools and spreadsheets cannot be used to design them successfully. This paper outlines the role of dynamic simulation in design of ion exchange systems. Examples are given for use of dynamic simulation in design and investigation of equipment based on consideration of the effect of input criteria such as expected ion loading and elution profiles. The methodology for dynamic modeling using IDEAS in design of multi column ion exchange trains operating in parallel is presented. Results shown include the non-steady state distribution of extracted metal and limitations imposed on operating conditions. These conditions include proposed sequencing of columns for loading and elution cycles, loading, elution and recycle flow rates as well as size and choice of related ion exchange plant equipment.

Jan 1, 2003

By Li Cheng

The SKS copper smelting process was jointly developed by Shuikoushan Mining Corp. and ENFI (Beijing Central Engineering and Research Institute for Non-ferrous Metallurgical Industries) in China. It is a new bath copper concentrate smelting process with oxygen enriched air. The pilot plant testwork was completed successfully in 1993. SKS has demonstrated to be an advanced bottom blown smelting process. This technology got the First Class Prize of Scientific and Technological Progress awarded by CNNC (China National Non-ferrous Metal Industry Corp.) in 1994. The SKS process has significant capital and operating cost advantages. Its environmental and industrial safety and hygiene performance represents a substantial improvement when compared to conventional technologies. The technology has generated great interest in the Chinese metallurgical industry. Feasibility studies and basic designs have been carried out to incorporate in retrofit and green field smelter projects in China and abroad. This paper describes the history of the pilot plant operating data (50 tonnes dry feed/day), and discusses the features of the SKS technology, its application and possible future trends.

Jan 1, 1999

By Nathaniel Arbiter

The first ammonia leaching plants, applied to copper carbonate and native copper tailings in 19 15, were followed more recently by research and development of flowsheets for ammonia leaching of sulfide concentrates. These were applied to two commercial plants. Anaconda's Arbiter Plant started up in 1974 with a design capacity of 36,000 tons/year of cathodes, to be produced by ammonia leaching with oxygen, followed by solvent extraction and electrowinning. The plant shutdown in late 1977 as a result of high maintenance and operating costs, partly due to harsh winters; to complications associated with sulfate disposal; and to changes in mineralogy. BHP's Coloso plant in Chile was designed to produce 80,000 tons/year of cathodes by leaching part of Escondida's concentrate production. Using a similar flowsheet but with air and low temperatures to avoid sulfate production, it started up in late 1994 and shutdown in mid-1998, after failing to reach cathode design capacity, and experiencing problems with its technology. The paper reviews the technologies and also alternative methods for overcoming the problems.

Jan 1, 1999

By N. Kanarin

A thermodynamic study is reported on the chlorination of Fe(1-x.)O, Fe2O3, Cr2O3, MgO, Mg2SiO4 with chlorine in the presence or the absence of reducing atmospheres. The reactivities of these compounds as well as that of Mg3Si2O5(OH)4 using Cl2+N2, Cl2+air, and Cl2+CO gas mixtures were studied by non isothermal thermogravimetric analysis between 20 and 1000 °C. The same solids were chlorinated in a horizontal experimental set, during two hours between 350 and 1000 °C, in reducing and oxidizing atmospheres: The chlorination products were examined by XRD and SEM, and possible reaction paths were examined. Results indicate that the carbochlorination of these solids was better than their chlorination; Furthermore, the carbochlorination was performed at lower temperatures than those of the chlorination. Finally, the reaction extent was higher in the case of carbo-chlorination of these compounds. Based on these results, a process was suggested for the selective recovery of chromium compounds from the chromite concentrate.

Jan 1, 1995

By J. R. Goode

Up to one half of neodymium and praseodymium production, key ingredients in permanent magnets, is produced illegally. About 60% of cobalt production, critical in lithium-ion batteries and other applications, comes from central African states, and much of it is produced illegally. Tantalum, important in modern electronics, is also primarily sourced from central Africa and, again, much of it illegally. Illegal mineral production, as exemplified here, is often used to fund armed conflict. Furthermore, it is typically conducted with scant regard for human rights and environmental protection. It also leads to depressed prices which in turn limits the possibility of legitimate producers entering the market. Systems of traceability and provenance, along with cooperative supply chain participants can limit the production of illegitimate material and thereby improve conditions in the countries of origin and reduce downward pressure on prices.