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By Xinghui Meng

The leaching behavior of platinum powder in .iodide solutions under oxygen pressure in an autoclave was investigated. Ammonium salts were added to the leaching solution at neutral pH as a key lixiviant for platinum. The effect of temperature, partial pressure of oxygen, concentration of iodide and of arttmonium salts on the dissolution rate of platinum was examined. Under experimental conditions, the leaching behavior of platinum powder exhibited a complex reaction mechanism. A precipitate was found during the leaching process and was identified to be platinum ammine iodide, Pt(NH3hI4. The dissolution rate was controlled by a series of chemical reactions, the equilibrium concentration of the platinum ammine iodide being responsible for the ultimate limit to the recovery.

Jan 1, 1996

By Song Ning

The main mineral constituents of phase-transformed chalcopyrite are CuS and FeS2. CuS is more soluble than FeS2 in an acidic CuCl2 solution with presence of excessive NaCl, so that FeS2 could be removed as solid residue from a leached solution. The experimental results showed that the efficiency of the copper leaching is heavily determined by the following two factors: a) The degree of the chalcopyrite phase transformation to CuS and FeS2 b)The concentration of Cl during the leaching, specifically whether there is enough excessive Cl existed. I t was found that when the Cl in the solution is not excessive, the slowest step of the leaching is the dissolution of Cu2Cl2.

Jan 1, 2006

By D. L. Jones

The leaching of natural chalcopyrite was studied in both ferric sulfate and ferric chloride solutions. The chemistry of the two reactions is quite different, with substantial sulfur oxidation occurring only in sulfate solutions. Ferric chloride is a more effective reagent, for the leaching rate is greatly increased with finer particles and higher (Fe+++), and unaffected by high (Fe++); none of these advantages are found with ferric sulfate. In addition, the morphology of leaching appears to be different, with ferric sulfate leaching preferentially along fissures or grain boundaries. The kinetics were found to be linear over an extended period, rather than parabolic as reported elsewhere. An explanation of the observed phenanena is proposed using the electrochemical theory of leaching, and experimental measurement of the mixed potential of the mineral during leaching.

Jan 1, 1976

By R. Menge, N. Basin, M. Sibony, J. Lecadet, S. Schmidt

In 1996, Metaleurop replaced its conventional sintering and blast furnace lead smelting activity in Nordenham, Germany by Sirosmelt/Ausmelt technology. Following some alterations to the process and the equipment, the bath smelting plant reached its design capacity for the treatment of lead concentrates, lead sulphate paste from spent batteries, secondaries and internal by-products. A reliable metallurgical process has been established, and thus higher process stability has been achieved, increasing simultaneously the refractory life. Nevertheless, improvements are needed to control the process with a better automation system and reliable expert-systems, because of the intensity of the smelting process. The introduction of the Sirosmelt process for the pyrometallurgical production of lead instead of the prior conventional process has also demonstrated the following advantages: reduced emissions of heavy metals and gaseous compounds, reduction of the specific energy consumption, minimization of residues and a reduction of staff and maintenance costs. The environmental performance of the plant meets the requirements of the German regulations.

Jan 1, 2000

By Arthur S. Klein, Hugh R. Lowry

"The Levitation Casting Process is a new continuous casting method that uses an electromagnetic levitation field, instead of a mold, to support and contain a column of solidifying metal. By counteracting gravitational forces and hydrostatic pressure on the metal column, this process eliminates friction and adhesion at the interface between the solidifying metal and the cooled walls of the casting chamber. The process inherently provides high casting speeds, excellent dimensional control and smooth, continuous emergence of solidified product from the top of the casting chamber.Of major importance is that the electromagnetic field produces an intense stirring of the liquid metal both before and during solidification. As a result of this stirring, the cast product has a homogeneous, equiaxed, fine grain structure generally suitable for immediate drawing or other forming operations without the need for hot rolling or other expensive additional processing.This paper reviews the fundamentals of the Levitation Casting Process, results obtained in casting various pure metals and alloys, and the production sized system at Lowell, MA, that uses this process. IntroductionThe Levitation Casting process was specifically developed to meet several requirements including:• Economic at low casting rates• Usable with pure metals and alloys• High, uniform product quality suitable for fine wire drawing or cold rolling into flat strip and tape• Easy cast product shape and size changes• Process inherently stable and easily automatedIn meeting these criteria it was also desired to retain the advantages of General Electric's well known Dip Forming continuous casting process; namely the inherent ""fail-safe"" properties of upward casting, solidifying metal by means other than pressure contact with a cooled mold, and use of a sealed furnace, casting chamber and cooling tower, filled with a protective atmosphere, to prevent oxidation of the molten metal or cast product."

Jan 1, 1988

By Shiwei Sun, Hongxu Li, Xiangxin Hao, Xie Yang

"Environmental impact assessment of copper metallurgical processes will soon become a compulsory activity in the future. The goal of this work is to analyses the copper metallurgical processes including pyro-metallurgy and hydrometallurgy based on the life cycle assessment method implemented in GaBi software. The evaluation indicators such as global warming potential (GWP), acidification potential (AP), photochemical ozone creation potential (POCP) and human toxic potential (HTP) are taken into account. The results show that the major environmental impact phase in pyro-metallurgy derives from beneficiation because of the largest material and energy consumption. It is also shown that copper hydrometallurgy has significantly lower environmental impact than pyro-metallurgy. Based on the evaluation results, some corresponding optimization methods are recommended to reduce environmental impact.IntroductionCopper is an important metal in modem society due to its wide variety of uses, including electrical wiring, heat exchangers, piping and roof construction and increasingly consumer electronics. Demand for copper has increased dramatically over the past decades, driving production rates almost exponentially. Annual production of copper was estimated to be 20 million tonnes in 2012 with Chinese production at about 6.06 million ton in 2012P1. The production process of copper has environment impacts that often go unnoticed by the producer. Higher production, coupled with declining ore grades, is placing increasing pressure on the natural environment.Sound environmental management helps producers improve their manufacturing technique. LCA is a well-established tool for assessing environmental impact potential and can be readily adapted to map impact potential over time, which can be used to quantify the environment impacts of a product or a process [21. This is achieved by creating an inventory of all the energy and material flows used in the process's life cycle. The results of an LCA can be used to improve the operation of a process so that they have less impact on the environment."

Jan 1, 2014

By Zhiqian Zhang, Chao Wu, Chao Li, Hongxu Li, Yu Chen, Xiangxin Hao

"In this paper, the life cycle assessment models for automobile lightweight materials including high-strength steel, aluminum alloy and magnesium alloy are developed by Gabi software. The evaluation models and evaluation indicators such as acidification effects, rich eutrophication effect, ozone layer depletion effects, global warming, resource consumption and formation of ozone potential were taken into account. It is shown that the effects of acidification and ozone formation are mainly derived from the run phase of high-strength steel and they have strong environmental impact load. While considering the entire life cycle with materials production phase and resource consumption, the aluminum and magnesium alloy appe art o have large r environmental load than high-strength steel. Base d on the evaluation, some optimization tips are proposed.IntroductionAs the increasing of car ownership, automobile has its two sides. One which is the convenient, efficient and fast traffic vehicle; the other is aggravating energy consumption, emissions and environmental pollution. The car industry faces heavy pressure with energy saving, safety and environmental protection. Nowadays, the main study ways for automotive energy-saving and environmental protection are power system improvement, alternative energy sources and technologies. For limitation of technique, development cycle and market share, the development of car is little progress at this stage and the application has been restricted. And another important way is the lightweight of vehicle. Usually there are three ways to get the lightweight automobile body structure, automobile body structure optimized design, using advanced body manufacturing technology, development and application of lightweight high strength body material.The life cycle assessment (LCA)[1lis commonly used to evaluate environmental factors and potential environmental impacts of products and services. As an environmental management tool of product-oriented, it becomes increasingly popular in industry. In this study, the concept of LCA and GaBi software was used to develop models for the three automotive lightweight materials, evaluate the environmental impact and make horizontal and vertical contrast by choosing variety of evaluation systems and indexes."

Jan 1, 2013

A full-scale test of chalcocite heap bioleaching was undertaken at Straits? Nifty Copper Operation. Straits worked closely with the CSIRO to investigate the chemical and biological changes over the life cycle of this chalcocite heap bioleach system. Results indicated nearly 80% copper recovery was achieved in just over 300 days. Significant changes in iron chemistry and microbiological activity were detected. Temperatures in the heap reached as high as 70 ºC during the time of maximal copper recovery rate. The dominant cultivatable bacterial strains were typical mesophilic bacteria, however, naturally occurring moderately thermophilic bacteria were detected by culture and culture independent molecular (PCR followed by denaturing gradient electrophoresis [DGGE]) and signature lipid methods. Signatures for the iron and sulfur-oxidising species Acidithiobacillus ferrooxidans and Sulfobacillus spp., as well as the moderately thermophilic heterotroph Alicyclobacillus sp. were detected. Biomass was greatest in ?warm? but not ?hot? parts of the heap, and Hyperthermophilic Archaea were not detected.

Jan 1, 2003

By P. F. Stratton, M Huggahalli, N Saxena

"Several studies have been carried out to determine how the optimum atmosphere conditions in the heat treatment of metals can be established for a given product by using different gas injectors and varying atmosphere flow rate and composition. The most common approach taken to gain insight into furnace atmospheres has been to use commercial computational fluid dynamics codes and examples of their use are shown. However, the complexity of these codes, the difficulty in establishing boundary conditions, their cost and computational demands limit their usability in solving day-to-day production problems.A simplified, web-based model of a furnace atmosphere is described where the conservation equations are solved to determine the composition profiles of the atmosphere in the furnace. Although the model is restricted in scope to certain types of furnace, it is shown to give better results than CFD when boundary conditions are uncertain. The application of the model to the understanding of existing furnace conditions and to determining ways of optimising the use of gases are discussed. IntroductionThe important role of protective atmospheres during heat treatment of metals, furnace brazing of assemblies and soldering of printed circuit boards is well established. The atmosphere in the furnace prevents air ingress and oxidation of the parts, helps flush away any flux or binder from braze and solder pastes and provides an important mode of heat transfer [1]. In a batch furnace having typically one or two gas injectors, the gas utilisation and process can be optimised by minimising air leaks and mantaining atmosphere homogeneity with fans or other atmosphere circulation techniques. In a continuous furnace, however, atmosphere optimisation is more difficult as furnace inlets and exits can also let in air. The atmosphere requirements of different stages of heat treatment, brazing or soldering vary [2]. Achieving these atmospheres in different sections of the open-ended furnace is a relatively complex task. Methods such as atmosphere zoning and the use of physical curtains and gas injectors have evolved with time, though it is hard to predict how effective these techniques will be for a given furnace and process. Experts in the field tend to rely on experience and rules-of-thumb rather than scientific method to achieve the required results."

Jan 1, 2001

By A. R. Laplante

Recent developments in gold metallurgy are used to illustrate how the interface between gravity recovery and hydrometallurgy has evolved in recent years. Of particular interest is the use of gravity recovery to produce high-grade concentrates that can be subjected to intensive cyanidation. It is expected that a growing proportion of gold production, possibly close to 50% in certain countries, will follow this route. Other examples of the interaction between gravity recovery and cyanidation are also provided. Implications for new and renewed research directions are discussed.

Jan 1, 2003

By M. Soltanieh

The liquidus surface? and tie-lines in the nickel-cobalt-sulphur ternary system have been determined between 1<273-1573 K. The experiments were conducted by equlibrating the liquid sulphide with the metallic alloy phase. The liquid sulphide phase was sampled and chemically analyzed. The alloy was analyzed by electrol} microprobe. Combining the present results with the.avai1abl~ literature data, the thermodynamic properties of this system were calculated.

Jan 1, 1998

By Dan A. Mackie

Continuous leaching of precious metals ores in a vat is possible using a jigging technique. This patented method promises to be competitive with heap leaching, particularly in northern climates, difficult terrain, high precipiptation regions, and environmentally sensitive areas. The paper discusses test work to date, plans for pilot plant testing and basic economics

Jan 1, 1990

By Q. Chen

The magnetic properties and phase evolution of Nd-lean and/or boron-rich melt- extracted ribbons of Nd98Fe90.2xBx, where x = 6 through 11, have been studied using XRD, DTA, TMA, and VSM. The off-stoichiometric Nd2Fe14B compositions cause additional phases to be present after crystallization and affect the magnetic properties obtained. The crystallization temperature of this alloy series rises with the increasing) boron content. In addition to Nd2Fe14B and a-Fe, Fe3B is detected. It is found that increasing the boron content reduces B, within this composition range. The magnetic properties are directly associated with the relative magnetic phase content in the samples.

Jan 1, 1997

By S. S. Bogomolov

The relationship between the magnetic properties and micro- structures of Pr-Fe alloys rapidly quenched by melt-spinning and highly undercooled by containerless processing in the Cambridge drop-tube was studied. The maximum measured coercivity, Hc, of as-cast samples was 4450 Oe for Pr-2 wt.%Fe. However, rapid quenching or melt undercooling decreases coercivity for hypo- eutectic alloys (<10 wt.%Fe) and increases Hc for hyper-eutectic systems.

Jan 1, 1992

By C. D. Chapman

Current regulations regarding the landfill disposal of asbestos containing wastes are inadequate to ensure there are no ground water or airborne emissions. Accordingly, there is growing recognition that asbestos wastes can only be safely disposed of by using techniques that destroy the hazardous fibres. An innovative high-temperature plasma arc technology (The MAGRAM Process) is being developed for the recovery of magnesium metal from asbestos together with supplementary magnesia containing feedstock. The furnace will operate in. open bath mode with aluminium and/or ferrosilicon being employed as reductant. An important advantage of the process is that magnesium vapour within the furnace will be generated close to atmospheric pressure rather than at reduced pressure under which existing processes operate. Thermodynamic modelling work has been undertaken to define the range of slag composition and furnace temperature under which magnesium production at atmospheric pressure is feasible. The effect of slag chemistry, reductant addition, and temperature on product quality and yield have also been investigated and key aspects have been tested on bench scale. A 300 kW pilot plasma furnace unit has been employed for the treatment of calcined asbestos wastes. Aspects of design and operation of the unit are detailed. Acknowledgement: This work is substantially financially supported by the European Communities under the Industrial and Materials Technologies (Brite EuRam H) Research and Development programme.

Jan 1, 1995

By Joseph Bloch

The hydriding of bulk metals and alloys is a gas-solid reaction in which a hydride product layer is initially nucleated adjacent to the gas-solid interface and continues to grow until a complete transformation of the parent (a) phase into the hydride phase. The combination of measurements of the overall hydriding kinetics of samples having defined shapes and dimensions, together with examinations of partially hydrided samples, enables the presentation of the reaction rate in terms of an appropriate reaction model. A common and important type of topochemical development of the hydride in bulk metals and alloys involves a hydride layer formed on the metallic surface. The continuity of the layer can affect the reaction rate. The rate of hydrogen absorption in a sample, in the presence of a hydride layer, is usually analyzed using a model combining several sequential steps in which the hydrogen is transferred from the gas phase into the reaction site. Coupling the flux equations across the layer under proper steady state conditions, results in a complex rate equation in which the steady state rate of hydrogen absorption (proportional to the hydride layer velocity) is expressed in terms of the pressure, temperature, the rate constants of the sequential steps and the critical concentrations of hydrogen in the hydride. Generally, the rate constants of the individual microscopic processes are comparable in magnitude, so that the overall rate is not controlled by any of the specific sequential steps. However, there are two limit cases related to the first stage, the adsorption, for which the general rate equation is much simpler, namely, the fast and the slow adsorption approximations. Using this limit cases, equations are derived for the steady state hydriding rate of a given system. These equations provide means to anticipate the pressure dependence of the steady state absorption rate under low pressures, close to Peq and under very high pressures. At the low pressure regime both the fast and slow absorption cases yield linear pressure dependence. For the very high pressure range, it is found that the rate become independent of the applied pressure. The rate is given then by a combination of the individual rate constants of the system and the critical hydrogen concentrations. The model is shown to apply in several real cases, such as ZrCo, LaNi5 and titanium.

Jan 1, 2002

By F. W. H. Dean

A very sensitive sensor for the detection and measurement of hydrogen in solid steel is described. This technique is non-invasive and uses a collector to sweep the hydrogen emanating from a steel surface and feed to it sensor. This method is particularly sensitive, resolving fluxes to < 2 pI cm?2 S?I, with a linear measurement up to 1000 pI cm&apos;2 S?I, The collector is held on the steel substrate by magnets and it is shown that emanation of hydrogen from the steel is controlled by bulk diffusion of the hydrogen through the steel. The technique is demonstrated to have an excellent response time and reproducibility.

Jan 1, 2001

By J. E. Dutrizac

Fracture-exposed surfaces of sphalerite samples having five different solid solution iron contents ranging from 0.0 wt% to 14.8 wt% Fe were leached for 15 to 120 s at 100°C in 0.3 M Fe(S04)1.5 -0.3 M H2S04 media. The reacted samples were examined using X-ray photoelectron spectroscopy (XPS) which provides chemical state information on the first few nanometers of the solid surface. Surface compositions show that the leaching rate increases with increasing solid solution iron content of the sphalerite. Detailed evaluation of high resolution S2p spectra show that the leaching progresses via the formation of polysulphide species. Disulphide species were not detected in any of the experiments. Examination of the Zn2p and Fe2p spectra indicate little change in the chemical states of these elements over the duration of the experiments. Longer leaching times resulted in the generation of elemental sulphur. The ratios of elemental sulphur to dissolved ferrous ions and zinc suggest that less than 5% of the sulphide is oxidized to sulphate. Morphological studies showed that the elemental sulphur commonly formed at a few isolated sites, such as the grain boundaries. Furthermore, euhedral sulphur crystals were often identified. These observations suggest that at least part of the elemental sulphur forms via dissolved sulphide species which are oxidized in solution by ferric sulphate.

Jan 1, 2003

By Isabel Lázaro

A detailed study has been undertaken into the electrochemistry of the leaching of chalcopyrite in acidic solutions containing ferric ions. Mixed potential measurements have shown that the maximum potential achievable on a chalcopyrite disk in a ferric sulfate medium lies within the so-called passive or prewave region in the anodic behavior of chalcopyrite. The very low current densities due to the anodic oxidation of chalcopyrite at potentials in the region of the mixed potential has made studies of the initial stages of dissolution difficult. However a careful rotating ring-disk electrode (RRDE) study has enabled data to be obtained for the stoichiometry of the initial dissolution reaction to be obtained. Thus, in addition to the detection of soluble iron and copper as products in this potential region, a soluble sulfur species has also been detected. A comparison of the experimental with the expected collection efficiencies of the products on the ring has revealed that this soluble sulfur species is likely to be thiosulfate. The characteristic transient anodic behaviour of chalcopyrite in this potential region has been interpreted in terms of a rate limiting solid-state diffusion process. Thus, extrapolated rates based on reported measured solid-state diffusion coefficients for the mineral at elevated temperatures have been shown to be consistent with the potentiostatic current-time transients. Furthermore, comparative studies of the anodic characteristics of the copper sulfide minerals covellite and bornite has confirmed their greater reactivity in this potential region. The results of this investigation have been combined with a parallel study of the non-oxidative behaviour of chalcopyrite in order to derive a model for the dissolution process which is consistent with other published studies of the electrochemistry and dissolution of the mineral.

Jan 1, 2003

By Luis W. Pommier

The wastes of the plating industry are generated in the process of rinsing the plated objects and during the cleaning of the plating shops. High volumes of hazardous waters are neutralized on site producing recyclable water, generating a metal rich, hazardous, filter cake. Occasionally, a complete plating bath has to be discarded which increases the metal content of the filter cakes. These filter cakes are discarded as hazardous at a cost of over $ 250 per ton. The metals found in the cakes are generally copper, nickel and chromium or zinc, lead and cadmium, assaying from 2% to 15% or even higher content of each metal The metals and their contents are highly variable. Some plating shops discard their products directly to hazardous waste sites, others, have them collected by companies which consolidate wastes from several producers prior to discarding. These wastes, richer in metal content than mine ores, need neither mining nor crushing and grinding for concentration. The commonly found impurities in the mine ores, i.e.: pyrites, arsenic, and valuable metals which are present in minute quantities, are absent in the filter cakes. The processes available to selectively recover the metals from the filter cakes, are discussed based on their technical and economic merits. The flow-sheets include leaching, solvent extraction when required, and electrolytic refining. Examples, showing the separation of copper, nickel and chromium and also of zinc and lead in pilot plants, show the technical and economic viability of the processes.

Jan 1, 1996