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By Helena Byrdziak

Polish Copper Industry, located in the Lepica-Glogów region and operated since the 1970's, includes four mines and two smelters, "Legnica" and "Glogów", the latter consisting of "Glogów" I" and "Glogów II" both having different technologies. The "Legnica" and the "Glogów I" smelters using shaft furnaces, so sulfur elimination largely takes place during batchwise converting, resulting in fluctuation SO2-concentration between less than 1% up to 10% in the converter pas W the sulfuric acid plants. The ensuing difficulties of the past have now largely been overcome. Introduction of flash smelting at "Glogów II" with subsequent acid making by double SO2-conversion from the stable process gas, contributed significantly to further reduction Of SO2-emission. In 1994 a new double conversion sulfuric acid plant was installed at "Glogów l" as well as a "Solinox" desulfurisation plant at "Legnica", further reducing SO2 emission considerably, The next step towards this goal under consideration is a semi-dry desulfurization system for the "Glogów I" power station, SO2- abatement measures by KGHM and the results thereby achieved are presented.

Jan 1, 1996

By A. V. Tarasov

In order to improve the efficiency of hydrometallurgical processing of pyrrhotite concentrates, an integrated set of research has been carried out to investigate the use of sulfur dioxide in individual unit operations and as a leaching agent in the autoclave process as a substitute for oxygen. Treating iron-containing raw materials for production of nonferrous metals are based on the selective reaction of SO2 with iron sulfides and oxides. Iron is dissolved as sulfate, which can be treated in a separate circuit to produce iron-containing pigments or it can be disposed of after neutralization. Nonferrous and precious metals contained in pyrrhotite concentrate do not react with sulfur dioxide and remain virtually completely in the solid phase, i.e. high-grade sulfide concentrate to be treated by hydro- or pyrometallurgical methods. Elemental sulfur formed in the process of leaching is separated from the pulp in granulated form as a result of the use of special surfactants. The process of sulfide concentrate leaching with the use of sulfur dioxide is conducted at temperatures above the sulfur melting point (119°C) with distributed feeding of surfactant and under a partial pressure of sulfur dioxide of up to 0.3 to 0.5 MPa.

Jan 1, 2006

By N. A. Warner

Fundamental studies on the reaction of limestone or dolomite at high temperature with S02 are extended to the realm of large scale primary copper smelting. Whereas flue gas desulfurisation in the electric power utility industry is concerned with S02 concentrations normally less than 0.5 percent, high temperature smelting gases can have S02 levels approaching 100 percent. The reaction involved is very exothermic so proposals are made in this paper for returning the heat generated in sulfur fixation directly back to the copper smelting process. This integration leads to metal production with lower energy requirements than current technology. The anhydrite reaction product can either be disposed of locally with minimum adverse environmental impact or upgraded to a value-added product. It is assumed, of course, that no viable market exists to support sulfuric acid production.

Jan 1, 1996

By Peter K. Everett

One of the major driving forces behind the development of the Intec Copper Process has been the increasingly stringent regulations governing SO2 emissions and, in some parts of the world, a declining H2SO4 market. Other incentives include operating cost (9.2 US c/lb Cu), capital cost (US $1400/annual tonne Cu compared with smelter cost of US$3-4000/annual tonne Cu) and the ability to treat low grade and contaminated concentrates. With such advantageous features, widespread use of the process is expected over time, leading to the production of large amounts of residues containing around 25% elemental sulfur, together with approximately 50-60 % akaganeite (FeOOH) and the ganggue minerals originally present in the concentrate feed. This paper briefly describes the Intec process chemistry involved in the formation of elemental sulfur, thereby avoiding atmospheric sulfur dioxide pollution, and the investigations to be carried out either to extract it or to turn the residue into a valuable by-product while minimising any adverse environmental effects, The process is being developed jointly by a group of fifteen major international mining companies.

Jan 1, 1996

By D. Silva-Galvan, R. D. Morales, S. Gonzáelez-López, A. Romero-Serrano, G. Plascencia-Barrera, F. Chavez-Alcala

This work is focussed on lead decopperising by two techniques: conventional top addition of sulfur and injection of sulfur powder. It is found that the first method proceeds under equilibrium conditions and the second one depends on kinetic considerations. Experiments were carried out using 15 kg lead baths at two temperatures, 340°C and 380°C. The carrying gas used for the injection trials was nitrogen at flow rates of 6.3 and 18.6 L min- 1• The results show that 'decopperising process is more efficient at temperatures close to the melting point of lead for the sulfur top addition process, whereas high temperatures produce better copper removal for the injection of sulfur powder. Besides, the sulfur injection with the higher nitrogen flow rate (18.6 L min-1) produced higher decopperising rates. Thermodynamic and kinetic models are used to simulate this lead refining process.

Jan 1, 2000

By David B. George

Kennecott recently completed an $880 million modernization and expansion of its smelter and refinery to process all concentrates from the Bingham Canyon mine. This is the first application of Kennecott-Outokumpu Flash Converting. Molten material movement by overhead cranes is eliminated and high levels of oxygen enrichment result in very low process gas volumes and exceptionally control of sulfur oxide emissions. All existing in-plant hygiene, safety, and environmental regulations will be met and the smelter is positioned for anticipated more stringent future regulations. Sulfur capture is 99.9 percent resulting in sulfur dioxide emissions less than the 112 kg/hr Air Permit limit, making the smelter the cleanest in the world.

Jan 1, 1996

By A. P. Paiva

Studies focused on the recovery of precious metals by solvent extraction have recently increased. either to devise suitable solvents or to clarify the involved extraction mechanisms and kinetics. In this work, a comparison of the performance exhibited by triphenylphosphine (TPP), bis-(penty1thio)-ethane (BPTE) and triisobutylphosphine sulfide CI"I'BPS) in the extraction of silver from acidic chloride media is carried out. Extraction and stripping isotherms involving the three extractants are presented together with the results obtained on the selectivity of silver extraction against high contents of iron, copper and lead. Attempts to clarify the mechanism of silver extraction by TIBPS were performed by studying the distribution coefficient dependence on ligand and chloride concentrations. The effect of temperature on extraction and stripping is also considered. The interfacial tension for the system, measured with different concentrations of extractant in the organic phase, is analysed.

Jan 1, 1994

By John Demol

Monazite, a rare earth and thorium phosphate mineral, is one of the major minerals processed for extraction of rare earths. Industry practice for treating monazite concentrates is to use either a sulfuric acid bake or caustic conversion route. In the sulfuric acid bake, monazite concentrate is mixed with concentrated sulfuric acid and roasted. The rare earth phosphate mineral is converted to rare earth sulfate which dissolves in a subsequent water leach. As the bake temperature increases above 300 °C, thorium becomes less soluble. Although acid baking is practised in industry, the bake reactions are not well understood. A combination of chemical analysis, XRD and SEM-EDS was used to identify reaction processes occurring during sulfuric acid baking of a 93 wt% monazite concentrate between 200 °C and 800 °C. The effects of these reactions on the leachability of the rare earths, thorium and phosphate were also examined.

By A. Kontopoulos

The extraction of nickel and cobalt from low-grade greek laterites by sulfuric acid leaching has been studied. Batch and continuous mini-plant atmospheric leaching as well as pressure leaching techniques were employed. Atmospheric leaching at temperatures as high as 95 OC generally resulted in low Ni extractions (up to 82%), high acid consumption (650-850 kg/t ore or 80-100 kg/kg Ni) and high Fe co-dissolution (30%). Pressure leaching at 260 OC increased Ni extraction to over 98%, with minimal Fe co-dissolution (2.5%); acid consumption was 300 kg/t ore (31 kg/kg Ni). Detailed experimental results and conceptual flow sheets for atmospheric and pressure leaching are presented.

Jan 1, 1991

By R. H. Rubisov

Sulphuric acid pressure leaching of nickeliferous laterites has attracted considerable attention from the nickel industry during the past five years. The process is especially advantageous for limonitic laterites that mostly contain goethite, because iron precipitates releasing acid and thus rendering low acid consumption. It is also applicable to mixtures of limonites and saprolites, although at higher acid consumption due to magnesium. Effective process design requires the solubility of metals that precipitate during the process to be known. In the present work, determination of metal solubilities is based on a simple speciation program that assumes the presence of only one dominant complex for each metal. The thermodynamic data for the precipitation reactions are extracted from high-temperature experiments with monometallic systems published previously. The validity of the approach is then tested against mixed bimetallic systems, and finally applied to calculate the solubility of aluminium, iron and magnesium in laterite leaching effluents "at temperature". In both cases of limonitic feed and limoniticfsaprolitic blends, the prediction closely follows metal solubilities measured experimentally at temperatures from 230 to 270°C and at terminal he acidities ranging from 10 to 75 g/L.

Jan 1, 1999

By T. Ranki-Kilpinen

In the flash smelting technique, developed by Outokumpu Oyj, off-gases with dust load are directed into the heat recovery boiler (HRB). As the temperature decreases, metallic sulphates become thermodynamically stable. Sulphation of oxidic particles initiates. The release of heat causes an increase in particle temperatures, and soft sulphated particles can stick to the heat transfer surfaces. Dust accretion may form and cause operational problems. The objectives of the project are to study sulphation reaction mechanisms and kinetics of flue- dust particles under HRB conditions, and get more information for the flue-dust treatment possibilities. The sulphation behaviour of synthetic Cu2O particles (37-53 pm) was studied using a fluid-bed reactor of laboratory scale. The experimental parameters in the latest campaign were oxygen and sulphur dioxide contents of 2.5-10 vol-% 02 and 40-60 vol-% SO2 respectively and temperatures of 600-660°C. Samples were examined microscopically (SEM+EDS) and chemical analysis were conducted. The sulphation rate was found to have a maximum at the certain temperature, which was dependent on the gas SO2 content. Regardless of the level of SO2, a rise in oxygen content promoted sulphate formation.

Jan 1, 2002

By R. Nilsson

In the present work the sulphide capacities of Ca0-Mn0-Si0, ternary slags have been measured in the temperature range 1798 - 1873 K by equilibrating the slag with a gas-mixture containing CO, CO,, SO, and Ar. The results are compared with the data reported in literature. A theoretical model has been developed in the present work where the sulphide capacity is expressed as a function of the slag composition and temperature. The model enables the estimation of sulphide capacities of complex slags with a knowledge of the capacities of simpler systems.

Jan 1, 1994

By D. J. Brennan

A techno-economic study is in progress, examining process and product options for treating smelter gases containing various concentrations of sulphur dioxide. Key contenders have been examined within an Australian context using the following criteria: * Markets for products * Capital Costs * Operating Costs * Waste streams generated Product options considered thus far are sulphuric acid, sulphur, calcium sulphite and gypsum. The development of an appropriate overall framework for evaluating process and product options is discussed and findings thus far presented. The emerging techno-economic study offers promise as a constructive guide to future policy decisions by industry and government.

Jan 1, 1994

By Wankun Wang, Shixing Wang, Jinhui Peng, Zebiao Zhang

"Germanium leaching from germanium dust and fume was carried out using sulphuric acid. Response surface methodology (RSM), based on a five level, four variable central composite design (CCD), was employed to obtain the best possible combination of liquid/solid ratio (Xi: 2-10), leaching time (X2: 1-5 h), sulphuric acid concentration (X3:3.15-15.75mol/L) and leaching temperature (X4:50-90 *C) for germanium leaching. The obtained experimental data were fit to a one-order polynomial equation using multiple regression analysis and also analyzed by analysis of variance (ANOVA). The 3-D response surface plot and the contour plot derived from the mathematical models were applied to determine the optimal conditions. The optimum extraction conditions were: liquid/solid ratio of 10, leaching time of 1 h, sulphuric acid concentration of 15.75 mol/L, and leaching temperature of 87.8 'C. Under these conditions, the germanium leaching extent was 65.14%, which is in close agreement with the value predicted by the model. The samples were characterized before and after leaching using X-ray diffraction (XRD).IntroductionResponse surface methodology (RSM) is one of the relevant multivariate techniques which can deal with multivariant experimental design strategy, statistical modeling and process optimization [1-15]. It is used to examine the relationship between one or more response variables and a set of quantitative experimental variables or factors. This method is often employed after the vital controllable factors are identified. It is also used to find the factor settings that optimize the response. Designs of this type are usually chosen when a curvature in the response surface is suspected [6], The process optimization of the sulphuric acid leaching of germanium from germanium dust and fume has not been reported in the literature. Hence the present work intends to assess the effects of variables such as liquid/solid ratio, leaching time, sulphuric acid concentration and leaching temperature and to identify the optimum conditions using RSM. The characteristics of sample before and after leaching are assessed using the advanced analytical instruments such as X-ray diffraction (XRD)."

Jan 1, 2012

By Richard B. Diver, Mark D. Allendorf, Daniel E. Dedrick, James E. Miller, Roy E. Hogan, Andrea Ambrosini, Eric N. Coker, Anthony H. McDaniel, Nathan P. Siegel, Gary L. Kellogg

"Converting carbon dioxide and water to hydrocarbons is an attractive option for storing solar energy and, coupled with appropriate CO2 capture technology, for recycling carbon and impacting atmospheric CO2 concentrations. For any process, high solar-to-fuel efficiency is necessary for large scale viability and favorable economics. Thermochemical approaches for solar-to-fuel conversion are potentially highly efficient as they avoid the inherent limitations of photosynthesis and also sidestep the solar-to-electric conversion necessary to drive electrolytic reactions. Solar-driven two-step metal-oxide-based thermochemical cycles for producing the components of syngas, CO and H2, from CO2 and H2O are the basis of the “Sunshine to Petrol” project. Multi-cycle production of both H2 and CO has been demonstrated over several iron- and cerium-based compositions fabricated into monolithic pieces both in the laboratory and at the National Solar Thermal Test Facility. These compositions are being developed for deployment in a unique and continuous solar-driven reactor prototype, the counter-rotating-ring receiver reactor recuperator or CR5.IntroductionThe interconnected challenges posed by increasing global competition for petroleum and the increasing concentration of atmospheric carbon dioxide are now widely recognized. Meeting these challenges requires recognition that although hydrocarbon fuels are ideal energy carriers, they can no longer be thought of as primary energy sources. It is necessary to take the realistic view that our conventional fossil fuels are in fact “stored sunlight” in the form of “sequestered carbon.” This view leads to a search for options to use and store sunlight more directly.Sunshine to PetrolIn combusting hydrocarbons we unlock the energy for utilization, but we also release the carbon to the atmosphere. However, nature teaches us that with an appropriate persistent energy source, e.g. solar irradiation, it is possible to effectively reverse the combustion process and “reenergize” CO2 and H2O back into hydrocarbon form."

Jan 1, 2010

By Anja Pfennig, Axel Kranzmann, Sabrina Schulze

The CCS technique involves the compression of emission gasses in deep geological layers. To guarantee the safety of the site, C02-corrosion of the injection pipe steels has to be given special attention when engineering CCS-sites. To get to know the corrosion behaviour samples of the heat treated steel 1.7225 42CrMo4, used for casing, and the stainless injectionpipe steel 1.4034 X46Cr13 were kept at T=60 °C and ambient pressure as well as p=lOO bar for 700 h - 8000 h in a C02-saturated synthetic aquifer environment similar to possible geological on-shore CCS-sites in the northern German Basin. The isothermal corrosion behaviour obtained by mass gain of the steels in the gas phase, the liquid phase and the intermediate phase gives surface corrosion rates around 0.1 to 0.8 mm/year at ambient pressure and much lower about 0.02 to 0.2 mm/year at 100 bar where the C02 is in its supercritical state. Severe pit corrosion with pit heights around 4.5 mm are only located on the 42CrMo4 steel. Main phase of the continuous complicated multi-layered carbonate/oxide structure is siderite F eC03 in both types of steel.

Jan 1, 2013

Today’s world relies upon advanced green technologies that are made of critical elements with unique properties. Examples include rare earth elements (REEs) that are critical in the manufacturing of wind turbines and electric/hybrid vehicle batteries, key components of a greener future that face supply uncertainty and near zero recycling. To tackle their supply challenges, activities have begun for urban mining from waste electrical and electronic equipment (WEEE) that contain considerable amount of REEs, but their current level of recycling is less than 1%. Current recycling practices use either pyrometallurgy, which is energy intensive, or hydrometallurgy that utilizes large volumes of acids and solvents and generates large volumes of hazardous waste. In this study, we developed a novel and sustainable process to recycle REEs from WEEE, NiMH batteries in particular. The developed process relies on supercritical fluid extraction (SCFE) utilizing CO2 as the solvent, which is abundant, safe, cost effective, and inert. The effect of seven operating parameters, namely temperature, pressure, residence time, sample to chelating agent ratio, agitation rate, complex formulation, and methanol addition on REE extraction efficiency was investigated, and optimum operating conditions were determined. This work is the first to utilize a very efficient and safe process that runs at low temperature to extract metals from postconsumer products with minimum hazardous waste generation, while offering about 90% leaching efficiency for REEs. We expect our process to find widespread applicability in urban mining of REEs using green chemistry.

By Kafui Nyavor

Acid mine drainage (AMD) is presently the biggest single environmental problem facing the mining industry. New and expanding metal mines in most parts of the world have to demonstrate their ability to contain this problem to obtain operating permits. Conventional methods of controlling acid mine drainage have primarily been limited to collecting the drainage and neutralizing with alkaline materials which do not provide a permanent solution to the AMD problem. Since acid mine drainage results from the oxidation of sulfides in the presence of oxygen, water and iron-oxidizing bacteria, controlling any of these three factors contributing to pyrite oxidation provides a potential at-source remedy for reducing or preventing acid mine drainage formation. Physical properties such as hydrophobicity also play an important role in the attachment of bacteria, adsorption of oxygen, water, and other ions that subsequently lead to the oxidation of pyrite. In this communication, the suppression of pyrite oxidation by treatment with fatty acid amines (FAA) was investigated. The FAA treated pyrite samples were tested at various conditions of temperature and pressure. At an elevated oxygen pressure of 500 psi and a temperature of 600 C, less than 0.2% oxidation was obtained for the FAA treated pyrite samples, while over 1.2% oxidation was obtained for the untreated samples in 10 hours of oxidation time. Accelerated column oxidation tests at ambient condition showed that FAA mated samples reduced pyrite oxidation by at least 75% in 81 days.

Jan 1, 1994

By S. Uddin

An integrated device has been developed to measure sedimentation potential, conductivity and pH simultaneously of particulate systems. Maxwell?s model was used to calculate volume fraction of solid from the conductivity data. In this approach, all system variables are known and zeta potential can be calculated from Smoluchowski?s equation. The technique is validated by comparing zeta potential vs. pH for alumina and silica suspensions with electrophoresis measurements. The technique was extended to mixed alumina/silica systems. Sufficient column height along with size difference between the two minerals allowed gravity fractionation during settling. Sedimentation potential measured over time identified the transition from one mineral to the next. Using XRD analysis the results supported the correlation between surface charge and sample composition. This is a step towards characterizing surface charge of mixed systems of interest in mineral processing.

Jan 1, 2010

By Hiroshi Maeta, Takao Kino, Hirota Osono, Kikuo Matsusaka, Azusa Shida

"Prior to refine an ultra-high purity material, it is necessary to estimate the surface cleanness of a base material. In this report, the cleaning method of a surface for refining of an ultra-high purity aluminum has been studied. Aluminum sample of 99.999% purity was p9lished mechanically and electrically and washed with various solvents. Surface composition and a depth profile near the surface were examined. Based on the experimental results, surface structure of an ultra-high purity aluminum was discussed.IntroductionRecently, studies on high purity metals have become of interest, and we have reported .various properties of an ultra- high purity aluminum1- 2)In order to purify a metal, it is necessary to clean a work area and to make vacuous as possible. So, we are studying the purification of aluminum by an ultra-high vacuum refining system and a zone refining system set up in a clean room with cleanliness class of 1000.Now, in order to avoid a mixing of impurities into the refining metal, a surface cleanness of a base metal is very important factor. The purity of the base aluminum used our work is 99.999%, but the surface state of the base aluminum is not clear. Aims in this work .are to investigate the surface state and to obtain the cleaning method of the base aluminum.Experimental procedureSamples used in this work were 99.9% (3N), 99.99%(4N) and 99.999% (SN) aluminum produced industrially and 99.9999% (6N) aluminum purified by us."

Jan 1, 2000