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By Richard M. RusselI, Jerry Sweeney

"The disposal of Aluminum slag wastes continues to challenge an otherwise environmentally beneficial and highly desirable industry - Aluminum Recycling. Slag wastes contain soluble salts that can be reused in aluminum smelting. Reclaiming salt is a logical first step in eliminating slag waste.Reclaiming salt flux has been conducted on a limited basis in the United States for reasons of economy. Practical methods and rising landfill tipping fees will increase the number of plants which opt to recover salts from slag wastes.The authors share their experiences in the design, operation and startup of a commercial scale flux reclamation plant operated by Tennessee Aluminum Processors at Mt. Pleasant Tennessee. This paper identifies three elements that allow practical operations:• Minimizing Evaporator Heat Duty• Simplifying Evaporator Operations• Potassium Chloride Fortification of the Recycled Salt"

Jan 1, 2000

By E. Gervais

Modern life in inconceivable without zinc. Zinc provides the most cost-effective and environmentally efficient method of protecting steel from corrosion. Zinc is also used to power electric vehicles and computers, to make brass, automotive equipment, household appliances, fittings, tools and toys, and to support the building and construction industries. It is also used in pharmaceuticals and cosmetics, in rubber, in fertilisers and in animal feeds. The links between properties, applications and performance, as well as zinc demand and market dynamics, will be reviewed along with market development opportunities and successes. The presentation will also include a progress report on the five-year plan of the International Zinc Association to increase the global market for zinc, over and above the natural growth, by 500,000 tonnes/year by 2002.

Jan 1, 2000

By Luis G. S. Sobral, Gabrielle N. Bard

Copper sulphides Concentrates, from the flotation process of copper primary ore; contain, commonly, small amounts of precious metals, such as gold and silver. During the smelting process of those concentrate all gold and silver are practically in the blister copper, which is cast into anodes. Those copper anodes are electrorefined in an electrolytic system, where the electrolyte is an acid copper sulphate solution, where a high purity electrolytic copper is produced (>999,9/1000). The slime when submitted to an oxidative leaching process, using sodium hypochlorite and hydrogen peroxide as oxidizing agents, turn those metals into solution. This research practical work, apart from concentrating effort on the digestion of the anode slime, aims at evaluating the efficiency of the cementation process of the metals of interest for the separation of them to take place. 141

Jan 1, 2008

By D. Ducharme, J. Lenz

Operation of the Kidd electrolytic zinc plant commenced in 1972 with a cellhouse capacity of 105,000 tonnes of zinc cathode. The original cellhouse layout consisted of 42 parallel rows for a total of 588 cells. As leaching capacity increased, the cellhouse was expanded to 630 cells. Zinc cathode was manually stripped from plant start-up until the development of a mobile automated stripping system in 1994. Machine development continued until a second unit was placed in production in 1996, from which point, 60 % of the cellhouse was being stripped with the automated system. The final phase of the project was implemented in 1999 with the commissioning of two more automated strippers. This paper describes the implementation of the automated stripping system and its impact on cellhouse productivity.

Jan 1, 2000

By Philip Thompson

"Carefully planned laboratory test programs provide valuable data regarding the amenability of low grade gold ores to heap leaching. The most common laboratory test is the column leach test. The overwhelming problem associated with this type of test is the limit on the test column height. Most laboratories use a three (3) meter (10 foot) high column as a standard test due to building ceiling limitations, sample size limitations, etc. This paper presents a case study in which an ore sample was tested in a 1.5 meter, a three meter, and a six meter high column to determine the effect of column height on the test results. Other important factors such as sample preparation protocol, preliminary bottle roll testing to determine appropriate crush size, column diameter requirements, and leach solution analyses, are also discussed.IntroductionColumn leach testing has been used for years by many laboratories to determine the amenability of low grade precious metals bearing ores to heap leaching. However, the test work can be compromised by poor planning, misinterpretation of results, and extrapolation of data beyond the reasonable boundaries of the experiment. Preliminary test work should be performed prior to column testing. This preliminary work provides valuable information regarding the response of the ore to cyanidation and aids in the design of the column tests.The sample should be screened into various size fractions prior to testing. The fractions are assayed to determine the gold content of each size fraction and of the overall sample. The most valuable preliminary test is the bottle roll cyanidation test which is usually performed on five kilograms of coarse sample in a large rolling bottle which can accept material up to 50 millimeters top size. The residue from this test is screened at different sizes to determine the distribution of unleached gold in the residue. Comparison of the gold distribution in the leach residue with the distribution of gold in the feed at the same size intervals provides an indication of the appropriate crush size for the sample. The overall gold extraction from the sample at the crush size tested is also determined from these data. Lime and cyanide requirements can also be estimated from this test. The viscosity of the bottle roll pulp and the size distribution of the feed and leach residue can also suggest whether agglomeration of the ore will be required prior to column testing. Ores which contain significant amounts of clays (greater than 5 percent) will generally require agglomeration to prevent plugging of the test column."

Jan 1, 1997

By Jeffrey Shepherd, Scott R. Smith, Eduard Guerra

"Electrochemical and spectroscopic evidence for the dissolution of a Au electrode by meso-2,3- dimercaptosuccinic acid (DMSA) from an acidic LiCl04 electrolyte is presented. Near the potential of zero charge, DMSA was determined to form a stable layer on the metal surface but at more anodic polarizations, DMSA was displaced from the metal through an oxidative process. The anodic displacement of the layer from the electrode resulted in a small amount of Au that was detected in the electrolyte using atomic absorption analysis. The extent of Au dissolution, was monitored while holding the potential of the electrode for 24 hours at the thermodynamic Eo/H,O in LiCl04 electrolytes containing 10 mM DMSA. This routine resulted in detectable quantities of a soluble Au-DMSA complex in the electrolyte and the greatest leaching was observed at a pH = 2.0. At room temperature, the leaching rate was stable at 10.9 µg cm·2 hr·' however, upon increasing the temperature to 50.0°C, the rate of Au dissolution increased yielding an average rate of extraction of 40.1 µg cm·2 hr- 1. Interestingly, after the first 12 hours of leaching at 50.0°C, the leaching current decreased dramatically suggesting surface passivation which prevented further Au extraction. The implications of this process in the industrial leaching of Au will be discussed.IntroductionThe use of cyanide in the industrial process of leaching Au from ores has raised concerns regarding both operational safety and environmental issues surrounding the disposal of spent leaching eftluents in tailings ponds. Depending on the chemical nature of the processed ore, the spent solutions that are released into the tailings ponds can contain toxic cyanide, either dissolved or complexed with different metals and may pose serious risk to wildlife as well as freshwater contamination to nearby water systems. Because of these issues, some recent studies have focused on the exploration of more environmentally-friendly molecules to selectively leach Au with appropriate kinetics. However, to effectively leach Au into an aqueous solution, a suitable ligand that reacts to form a stable chemical bond with Au is needed to form soluble Au complexes that can be later recovered [I]. Recently several sulfur bearing alternatives have been shown to leach significant quantities of Au in aqueous solutions. These include thiourea [2], thiocyanate [3], and thiosulphate [4]. However, alkylthiols are also known to quickly form a stable covalent Au-S bond [5], but have been relatively understudied in term of their ability to leach Au in solution, even though some short chain thiols are water soluble and relatively nontoxic."

Jan 1, 2012

By Lin Yang, Minjun Tang, Shuishi Liu, Jianfeng Zhou, Linjiang Qing, Xiaolei Song, Yufeng Guo, Tao Jiang

"The dynamics of oolitic hematite magnetic roasting was studied. The results show that oolitic hematite magnetic roasting was controlled by the internal diffusion, and the diffusion coefficient was 9.018x10-7 m2·s-1when the oolitic hematite was roasted at 650°C. Magnetic susceptibility improves when temperature increases and roasted time prolonges under the condition of roasting at 650°Cfor 50min, with the magnetic susceptibility is 39.88%. CaF2 and Na2C03 can significantly improve the magnetic susceptibility at the same roasting condition, and the magnetic susceptibility was 63.35% and 57.99% respectively, thus the reduction of oolimic hematite was promoted.IntroductionWith the continual depletion of free-milling iron ores and its rising price, developing the abundant resources of oolitic hematite has become one of the main research areas. The oolitic hematite accounts for 10% of China's iron ore reserve, and it also accounts for 30% of red ore reserve in China [1]. In order to exploit the oolitic hematite, there are many beneficiation research methods, including fine grinding/selective flocculation/high intensity magnetic separation or flotation, high-gradient magnetic separation, low intensity magnetic separation/high intensity magnetic separation/reverse flotation, chloridizing roasting/acid pickling, magnetic roasting/leaching process etc [2]. However, the oolitic hematite is easy to slim and the valuable mineral is covered by the slim, because of the tiny granule of value mineral, then the ooides are formed due to the state of layer morphology formed by iron ore and ganaue minerals [3, 4]. Fairly good separation indexes were hard to be obtained by traditional separation due to its structural features, so the magnetic property of the iron minerals will be changed with the use of the magnetic roasting [5, 6], which result in hematite variably altered to magnetite and simplified technological process so that a good separation indexes will be obtained by using the low intensity magnetic separation. Therefore, in order to provide theoretical direction of how to use the oolitic hematite effectively through the magnetic roasting, the oolitic hematite of GuiZhou province was studied, which emphasized on researching the dynamics of oolitic hematite magnetic roasting."

Jan 1, 2013

By Qionghua Zhou, Wei Liu

"Nanocrystalline silver bulk material with average grain size of 20.3 nm was prepared by warmvacuum- compaction method. The as-prepared nanocrystalline silver was characterized by X-ray diffraction (XRD), differential scanning calarmeutry analysis (DSC), thermogravimetric analysis (TG), and 6157 type Electrometer test, respectivily. The experimental results show that the average grain size and microstrain of the nanocrystalline silver are 20.3 nm and 0.088%. The melting point and melting enthalpy are 1228.7 Kand 82.34 Jig, which are lower than that of coarse-grained silver by 6 Kand 22.6 Jig, respectively. The electrical resistivity of nanocrystlline silver increases with higher temperature when the range of temperature is between 233K and 293K. The electrical resistivity at 293 K is 1.475xlO -7 Q·m, which is higher than that of coarsegrained silver by a factor of 9.IntroductionN anocrystaline ( nc) materials or nano structured ( ns) materials are three-dimensional (3 D) bulk materials with average grain size typically smaller than 100 nm. Ne materials have been of great interest for their unique properties, such as superior tensile strength [1-2], high microhardness [3- 4], superplasticity [5-6], magnetically quasi-isotropic [7-8] , and so on, making them one of the most promising nano-scale materials with wide applications. Ne materials with average grain size of 5-10 nm were firstly fabricated by Gleiter et al. [9] in 1980s, using inert gas condensation (IGC) method. Unfortunately, the large surface to volume ratio creates a high surface energy component in the total free energy of the system and results in a metastable state in the materials. Therefore, due to the signfica nt disordered grain boundary regions, nanomaterials are thermally unstable and are subjected to a strong driving force for grain growth. The grain growth even occurred at room temperature [10].The conflict or deviation of measured date, e.g. strength, microhardness, thermal stability, partly due to the grain boundary ratio or the distribution of grain size, and partly derived from imperfections such as voids and microcracks while earlier processing techniques are known to result in incomplete dens:fication [11-12]. Therefore, the higher quality samples produced in subsequently years still show such a general trend."

Jan 1, 2011

By G Hope, C Young, R. N. Gow

"The presence of enargite (Cu3AsS4) is problematic in gold processing as it is refractory, increasing cyanide and oxygen consumption, and enviromnentally hazardous. Selective leaching and treatment of the arsenic would prove advantageous to conventional gold leaching methods. The reactivity of enargite samples from Montana, US and Quiruvilca, Peru were studied under alkaline conditions, pH range of 8-13, using a cyclic voltammetry corrosion cell setup. Raman spectra of the surface were taken during and after cycling to compare surface species against theoretical predominance diagrams. Under slightly oxidizing conditions, covellite (CuS) peaks were found on the surface in a short matter of time, above - 200m V vs SHE for pH 9-13, suggesting arsenic leaching, but for longer conditioning times, elemental sulfur peaks were also found, which created a passivating surface layer. By operating above pH 12, under reducing conditions, ~-500mV vs SHE, arsenic can be leached as a thioarsenate (AsS4-xOx3-), without sulfur formation.IntroductionEnviromnental limitations on pyrometallurgical processing of arsenic has pushed the desire to process enargite-, Cu3AsS4, bearing concentrates towards a hydrometallurgical solution. Attempts to process can be broken down into two categories - the co-dissolution of arsenic and copper under acidic conditions or the selective leaching of arsenic under basic conditions. The selective leaching of arsenic would preferably leave behind a chalcocite, Cu2S, or covellite, CuS, phase that would be more amenable to conventional processing methods of the copper and gold industries. These methods employ bi- or poly-sulfides to leach arsenic as Assl· [1-4], hypochlorite leaching [5-7], ammoniacal leaching [8] or fine grinding to mechanically activate the enargite surface and increase normally slow reaction kinetics[9]. This study looked into the surface formations of an enargite electrode under alkaline conditions, in a pH range from 8-13, as it cycled from -1000 mV to 1000 mV vs SHE. The understanding of the formations and under what conditions they form will be helpful in further development of any of the aforementioned processes."

Jan 1, 2012

By M. Frades, C. Frías, G. Díaz, A. B. Mejías

"In recent years, zinc recovery from flue dusts and other industrial wastes has been increased, offering to the market a large tonnage of secondary zinc oxides, which can not be processed directly to render high quality zinc because of the hazardous impurities and halogens content.The ZINCEXTM Technology has been commercially applied for more than thirty years and represents the most suitable solution to deal with secondary or crude zinc oxides due to its flexibility, simplicity, and cost-efficiency, allowing production of SHG electrolytic zinc and pure zinc sulfate salts thanks to the flexibility and selectivity of the zinc solvent extraction unit regarding to get rid of impurities.A dual plant able to produce electrolytic zinc and crystallized zinc sulfate has been engineered to provide a flexible and profitable solution to zinc market. A description of the study and the relevant achievements is presented in this paper.IntroductionZinc is a valuable commodity in the marketplace and can be recycled again and again and still maintain its physical and chemical properties. Zinc recycling offers both environmental and economic benefits such as reducing volumes of material that end up in landfills, saving energy by reducing the need for mining and smelting, and relieving environmental impact on the land and water, and conserving zinc ore [1].The supply of zinc able to be re-processed will be increasing from year to year according to secondary materials enter the recycling stream, and as a result, more recycled zinc will become available in the market. Thus, some existing zinc refineries are implementing an annexed treatment line to process secondary oxides in conjunction with primary zinc concentrates [2].The galvanized steel scrap is normally recycled in electric arc furnaces or in basic oxygen furnaces, which generates a large tonnage of zinc-bearing flue dusts (EAFD). Around one million ton EAFD is yearly produced at the USA and the EU, respectively. The flue dusts are treated commercially by pyrometallurgical ways such as waelz kilns, electrothermic furnaces, etc, to yield secondary zinc oxides that can not be processed directly to render high quality zinc because of the hazardous impurities and halogens content [3]."

Jan 1, 2008

By S. Aguayo-Salinas, J. L. Valenzuela-García, A. L. Leal-Cruz, M. I. Pech-Canul, M. T. Certucha-Barragán

"The aim of this research was to carry out a comparative and systematic study of the degradation of cyanide by hybrid natural/biodegradation and biodegradation methods using a mixture of Pseudomonas sp and Bacillus megaterium native bacteria. Bioreactors consist of filled columns with contaminated ore containing 100 ppm of total cyanide. In the biodegradation tests a mixture of bacteria was inoculated into the biodegrading solution. Results of cyanide degradation show a similar asymptotic behavior in both the hybrid (opened system) and biodegradation (closed system) methods; however, for the same period of time (72 h) the permissible maximum levels (1-2 ppm of cyanide) are only attained in the closed system. While in the closed system the cyanide levels are reduced from 100 to 1.5 ppm, in the open system, cyanide decreases from 100 to 2.4 ppm.IntroductionOne of the most important tasks of mining industry is the treatment of the wastes generated in mining operations. Accordingly, industrial waste waters and ores represent a complex problem and a great challenge. In addition to ethic and communitarian considerations, there are laws that prohibit or regulate the contamination of water and air. Moreover, they establish that the restoration of wastes must be considered as a necessary operation cost [1]. Currently this important problem is being addressed by the mining and metallurgical industries using different approaches; mainly they are focusing on the treatment of waste waters and ores generated by the leaching process in which cyanide is used as a leaching agent for the recovery of precious metals as gold and silver. Cyanides have toxic characteristics and thus negatively impact the environment when they are discharged to the ground without previous treatment. While there are some processes in current use there are others that have only been proposed and that allow cyanide degradation, transformation to less toxic compounds and/or the complete elimination of cyanide. The second group includes a variety of techniques that use natural, chemical and biological treatments. Natural treatments consist of the passive abandoning of the heap and of its washing with water. Since these processes are slow and generate great volumes of water partially contaminated, then other alternatives should be considered."

Jan 1, 2008

By M. O. Lai

"Metal matrix composite (MMC) with composition of Al-4.Swt.%Cu reinforced by IOwt.%TiB2 or ISwt.%SiC particulate has been successfully fabricated using powder metallurgy technique. Disk, compression and beam specimens were prepared with (a) layered structure containing ductile Al-4.Swt.%Cu with brittle Al-4.Swt.%Cu/TiB2 or Al-4.Swt.%Cu/SiC layers, and (b) homogenous constituent with composition of Al-4.Swt.%Cu/lOwt.%TiB2' The specimens for the fracture toughness measurement were built through three ductile-brittle-ductile alternating layers. For the beam specimens, the layers were built through brittle-ductile-brittle sequence. The brittle layer consisted of Al-4.S%Cu with fixed amount of reinforcement. Fracture toughness testing revealed an increase for layered composites although the total amount of the reinforcement was the same for all disk specimens. The increase in fracture toughness is due to the existence of ductile layers which manifests a strong influence on delaying the occurrence of fracture. It acts as a barrier to resist the propagation of crack and hence increases the fracture toughness of the layered MMC specimens, Delamination in the beam specimens was observed to be due to shear stresses. Fracture surfaces of both disk, compress and beam specimens were characterized using the SEM. IntroductionMechanical and thermal properties can be achieved by the incorporation of refractory secondary phases to constrain the plastic flow of the matrix in a metal matrix composite (MMC). The size of the reinforcement particulate incorporated must be in the range larger than the dislocation cell size and strongly bonded to the matrix (I). Particulate reinforced metal matrix composites hence provide high modulus, improved wear resistance and strength (2-4). Because of the incorporation of refractory phases which are generally brittle, the major limitation in the mechanical properties of MMCs is their limited ductility in comparison to their base metals. Cracks normally initiate from the reinforcement and voids (4, 5). Due to the lack of ductility, cracks propagate rapidly with increase in load. As a result, the interactions between reinforcement particles and propagating cracks have recently been of great research interest (6). In addition, volume fraction of reinforcement and aging condition of the matrix significantly affect the mechanical behaviour of MMCs. In the case of AI-3.5%Cu reinforced with varying volume fractions of SiC particulate, it has been found that the probability of particle fracture increased with increasing volume fraction of reinforcement (7)."

Jan 1, 1996

By Ehsan Vahidi, Fereshteh Rashchi, Amirhossein Shahnazi

"The pig iron from steel manufacturing plants contains a high concentration of vanadium-bearing materials smelted with iron ore. During the oxidation process of the molten pig iron with oxygen lances, vanadium transfers to the slag. In this research, recovery of vanadium from LD (Linz-Donawitz) converter slag of steelmaking plant was investigated. The leaching residue was characterized by XRD and XRF techniques. The maximum vanadium recovery was achieved at optimum leaching conditions of 70 °C, S/L: 1/15, sodium hydroxide concentration: 3 M and leaching time: 150 minutes. The dissolution rate increased with rising sodium hydroxide concentration and temperature and decreasing particle size. The experimental data are treated graphically to explain the kinetics of the vanadium recovery process using shrinking core model (SCM). As a result, the controlling regimes in the SCM were analyzed separately using liquid film diffusion control, solid product diffusion control, and reaction control mechanisms.IntroductionVanadium is commercially important as a constituent of several alloys and catalysts. Nowadays, vanadium is mostly recovered as a by-product from secondary sources or from industrial waste streams such as titaniferrous magnetite, fly ash, spent catalysts, and petroleum coke. Steelmaking operations are specifically concerned by this problem due to the production of a huge quantity of by-products [1]. These by-products, including LD converter slag, sludge, fly ash, spent catalyst, ash, and alloyed scrap, contain a notable amount of heavy metals which may cause environmental problems. Solvent extraction is one of the techniques being increasingly used for the recovery of vanadium [2]. Apart from vanadium ore, secondary resources such as titanmagnetite, ilmenite and slag from the ferrous industry are a major source of supply. The pig iron from steel manufacturing contains a majority of vanadium-bearing materials smelted with iron ore. In a heat resistant shaking ladle the molten pig iron is oxidized with oxygen lances, causing the vanadium to be transferred to the slag. Normally, the vanadium in LD converter steel slag (coming from Linz-Donawitz steelmaking process) is ca. 5% as vanadium pentoxide (V2O5). This slag is the world's principal raw material for vanadium production [3, 4]. Moskalyk and Alfantazi [4] reported that a roast-leach process is used in South Africa for the production of vanadium oxides from magnetite ores while some of the slag was converted to ferrovanadium. A portion of the slag was exported to Europe for the production of vanadium oxide. The researchers mentioned that alkaline roasting was the main process at that time employed to extract vanadium pentoxide from vanadium slags."

Jan 1, 2012

By L. L. Sutter

Fly ash is a by-product produced from the combustion of most hels including municipal solid waste. Currently, most combustion residuals are disposed of in landfills at a continually increasing cost and with questionable impact on the environment. Due to the presence of heavy metal compounds, municipal waste combustor (MWC) fly ash has the potential to leach these metals (e.g., lead and cadmium) above regulatory limits. The heterogeneous nature of MWC fly ash makes detailed characterization difficult. This research focuses on the identification of lead compounds in MWC fly ash. Samples obtained from the Olmsted Waste-to-Energy Facility in Rochester, Minnesota were examined in this study. The fly ash was fractionated into six size ranges and prepared as geological thin sections for analysis. The worked discussed in this paper involves using an electron microprobe analyzer to determine phase composition in MWC fly ash. In addition, backscattered electron imaging, digital image processing, and mineral liberation analysis software were used to determine phase distributions and phase associations as a function of particle size. Several lead containing compounds in several forms are identified. The results of this study show that lead can be identified in small sectioned particles which would not be apparent using normal backscattered electron imaging.

Jan 1, 1994

By M. C. Ruiz

The conventional pyrometallurgical methods to treat copper sulfide concentrates include generally, one or more oxidizing steps where the formation of SO2 gas can not be prevented. From the economical point of view and the nature of some of the processes in which SO2 is produced, its complete capture is not feasible; therefore an important fraction is released to the atmosphere as fugitive emissions. In this research, the reduction of chalcocite was studied in the presence of lime as an alternative method, which overcomes the pollution problems related to SO2 emissions. The effect of temperature, time, concentration of carbon and CaO on the reduction rate were studied. Among these variables, temperature affects most the reduction rate. Conversions over 95 % can be obtained in less that 20 minutes at temperatures over 1000 ° C. The measured partial pressures of the gaseous components indicated that the chalcocite reduction proceeded through the gaseous intermediate species CO, C02, and the overall kinetics was controlled by the Boudouard reaction. The kinetic model In(1-X)= kt fits well the experimental data. Apparent activation energy of 3 14 kJ/mol was calculated for the temperature range of 900 0C-1050 °C.

Jan 1, 1999

By Cody Burcher-Jones

The recovery of rare earth elements (REEs) through heap leach/in situ techniques from so-called ion adsorption clays (IACs) is attractive due to their inherent simplicity. However, the underlying mechanisms of these processes are poorly understood. In this study, the deportment of REEs in a typical IAC material has been investigated and was found to concentrate in the phyllo-layers of the clays, especially hallyosite, and was readily desorbed by various ion-exchange reagents indicating various potential routes to liberate them. Here we are reporting the use of seawater (0.5 M NaCl), spiked with various amounts of (NH4)2SO4, and found better extraction using a reagent mixture than NaCl on its own. Further, the leaching of REEs from a bed of clay material was investigated over time to understand the rate of transport through the stagnant material. Results indicate that REE release is likely to be controlled by diffusion through the clay material, while desorption in agitated systems is rapid. A degree of fractionation between different REEs can be observed during diffusion. Nonetheless, the successful operation of in situ leach operations for this type of material would depend primarily on how easily solution cocktails can be made to flow through the bed material.

By M. I. Zinigrad

A model of an ideal associated solution is presented. This model takes into account the existence of complexes of various compositions, sizes and geometries and allows calculating thermodynamic properties and phase diagrams of binary alloys. The model has been used formerly to calculate thermodynamic parameters and the position of the liquidus line for binary eutectic systems and also those having a stable compound in the solid phase. In all the cases the model parameters were not adjusted rather estimated from melting temperatures of the components. The recent studies dealt with the influence of arbitrary-stoichiometry associates on the equilibrium thermodynamic properties of liquid alloys. The application of the model to eutectic systems and systems having an unlimited solubility in solid and liquid states close to liquidus has been considered. It was shown that if the difference in melting temperatures of the components was small, different types of fusibility diagrams were possible: eutectic diagrams, cigar-shaped diagrams or diagrams with upper or lower azeotropic points. Peritectic transformations could take place when the difference in melting temperatures of the components was large. The present work is devoted to calculation of phase diagrams and thermodynamic properties of binary systems on the basis of chrome.

Jan 1, 2006

By Pekka Taskinen, Hannu Johto

"Copper sulfide concentrates often contain impurities such as lead and iron. The phase stabilities of the sulfide impurity systems in metallurgical process conditions are in many cases unsatisfactorily known. Thermodynamic information of a system gives better understanding of its behavior of metal making processes, but also has effects on the economic and environmental factors of the production process. In this study, isothermal equilibrium and quenching experiments of the stable phases of the system Cu2S-FeS-PbS at 700 and 900 °C were carried out and based on the experimental results, Gibbs triangle of equilibrium phases of the system was outlined.IntroductionThe knowledge of stabilities of phases and the thermodynamic properties of many sulfide systems in the temperature range of 500-1200 °C are quite limited. Especially, the knowledge of liquidus surfaces of multicomponent sulfide systems is essential for making many metallurgical processes more environmental friendly and allowing the utilization of complex concentrates. In this work, the aim was to investigate the phase stabilities of the quasiternary system CU2SFeS- PbS using evacuated silica ampoules. Of greatest interest were the properties of the liquidus surface in the system, in order to be able to predict better the formation of a liquid phase in metallurgical processes."

Jan 1, 2012

By Huang Kai

Uniform needle-like and spherical nickel oxalate particles were prepared by the chelating precipitation process, which was based on the reaction of oxalate acid and the solution of ammonia nickel chloride. The molar ratio of ammonia to nickel ion in the mixed solution is essential to determine whether the spherical or needle-like particles are formed, which means actually the concentration of ammonia is the key to determine the growth mechanism. When oxalate acid is added in the form of solid, it may act as the nucleation interface for the eariy-precipitated substance and so induce the formation of spherical particles. The PVP agent can improve the dispersing degree of the needle-like particles and higher reacting temperature leads to larger particles. The composition of the needle-like particle consists of ammonium and nickel oxalate instead of the pure nickel oxalate.

Jan 1, 2003

By Justin Karl, Ali Gordon, James DeMarco, Yongho Sohn

"Aluminum metal-matrix composites are lightweight materials that have the potential to supplant steel in many applications. The current work helps to identify the parameters that confer maximal strength and ductility. Torsion tests were performed on the as-cast aluminum metal-matrix composite A359-SiCp-30% at a variety of temperatures and twist rates. Dependence of material properties on temperature and strain rate were identified from equivalent stress-strain curves constructed from the reduced data. Examination of the microstructure was performed on the as-cast material and on fracture surfaces. A temperature-and strain rate-dependent constitutive model was applied to simulation of the mechanical response of the torsion specimen. Trends in material properties corroborate and extend trends identified previously under tensile loading with regard to temperature and strain rate dependence. Shear properties of simulated specimens agree with properties obtained through experimentation.IntroductionAluminum metal-matrix composites (A1-MMCs) have become increasingly popu1ar in recent years. While unreinforced aluminum alloys have low densities and high ductilities, they are not suitable for many applications due to their lack of strength and stiffness. To provide added strength and stiffness while maintaining favorable densities, it has become common to reinforce aluminum alloys with silicon carbide in various forms, although usually the inclusions are in the form of whiskers or particles. The result is a composite material with superior specific strength and stiffness. While whisker-reinforced composites are expensive due to the necessity of processing by nonstandard techniques and have low transverse properties when rolled, particle reinforced Al-MMCs have transverse material property values almost as high as the longitudinal properties and are not as expensive to process as whisker-reinforced Al-MMCs [1]."

Jan 1, 2012