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By Kaixi Jiang, Lan Li, Bang Wei, Haibei Wang, Yaping Feng

"China is currently the world's largest copper producer. In the last five years, 950 kt/y of smelting capacity was commissioned. Currently, about 1200 kt/y smelting capacity is under construction and about 2000 kt/y smelting capacity is under feasibility study. Ausmelt/ISA smelting and flash smelting technologies were commonly adopted in China. After the double-flash-smelter was first adopted in 2004, three new double-flash-smelters are scheduled. Recently, two new copper smelting technologies were developed in China. One is an improved bath side-blown smelting process, and another is the SK.S bottom blowing process. Both technologies have been in practice for over three years and have achieved good technical performance. Approximately 500 kt/y new smelting capacity in China and India will adopt these technologies. Both technologies have the advantages of low investment cost, low energy consumption and high flexibility for complex raw materials. This paper reviews ""green"" copper smelting projects in China and introduces the practices of the two new Chinese smelting technologies.IntroductionPresently, China is the largest copper producer in the world. As far as the smelting of copper is concerned, there are many smelting processes applied in industrial production, such as flash smelting, Noranda smelting, Ausmelt smelting, Isa smelting, the Mitsubishi process, Vanukov smelting, silver copper-smelting, SKS smelting, both side-blown smelting, traditional blast furnace smelting, electric furnace smelting, reverberatery smelting and so on . Except the last three traditional processes that are eliminated because of their failure to meet the requirements for environmental protection, all of the other above-mentioned methods are advanced smelting processes adopted nowadays."

Jan 1, 2012

By J. J. Rush

Neutron scattering and analysis techniques are extremely powerful, often unique, probes for the characterization of the amount, location, bonding states, and dynamics of hydrogen in all classes of materials. Developments over the past decade at the NIST Center for Neutron Research and elsewhere have greatly increased the sensitivity and dynamic range of neutron methods. In this paper, we provide a flavor of the capabilities of modem neutron instrumentation for the study of hydrogen in a number of technologically interesting systems, including metal hydrides, fuel-cell materials, fullerenes, and disordered carbons.

Jan 1, 2002

By Amy Nelson

In the electrolytic production of zinc, cobalt is removed from the zinc electrolyte by cementation with zinc dust prior to electrowinning. Although the thermodynamics for this reaction are favourable, kinetic barriers to cobalt reduction render the method almost useless in practice unless activators such as copper and antimony or arsenic are added. There is a large body of work studying the effect of these additives, yet the mechanism by which they act is still poorly understood. Even when the target conditions are met, zinc dust consumption is excessively high: satisfactory operation requires up to 300 times the stoichiometric amount of zinc dust. The objective of this work is three-fold: (1) to examine the effects of activators and elucidate the characteristics that make a good activator; (2) to identify new additives that could lead to a more efficient purification process; and (3) to test the new additives with synthetic and real electrolyte solutions. The present paper gives a status report on this project.

Jan 1, 1998

By K. G. Wang, M. E. Glicksman, P. Crawford

"We formulate the mathematical solution to late-stage multi particle diffusion in finite systems. The transition from finite system behavior to that for an infinite system is established. Large-scale simulations are reported regarding the dynamics of phase coarsening. Even in the case of a small volume fraction (Vv = 10-4), the particle size distribution is broader than that for the well-known Lifshitz-Slyozov limit at zero volume fraction. We also report the first simulation studies of extremely low volume fraction, for which corresponding experiments, as well as other simulations, do not exist at present for comparison. However, in the case of moderate volume fractions (Vv = 0.1), the fiucutations in the volumetric growth rate of particles are extracted from our simulations. These simulations provide additional insight into the statistical nature of diffusion interactions, including multiparticle stochastics during microstructural evolution.IntroductionPredicting microstructure evolution in alloys remains one of the cornerstones of materials science. Phase coarsening is a common process in microstrucural evolution that leads to a decrease in the excess total interfacial energy of the system. The system typically consists of separate and identifiable units, or domains, such as second-phase particles distributed in a matrix. During phase coarsening, larger particles grow at the expense of small particles. Over time, this ""competition"" results in an increase in the average size of the particle population, and in a concomitant decrease in the number of particles.Particle size and microstructure of many cast alloys depend on similar coarsening processes. Indeed, properties of these materials, such as strength, toughness, ductility, and electrical conductivity, depend on the material's average particle size and particle size distribution (PSD). Understanding and controlling microstructures in two-phase systems are clearly of widespread technological importance."

Jan 1, 2001

By Tsutomu Yamamura

The electrolytic reduction mechanism of rare-earth chlorides such as LaCl3, CeCl3, NdCl3, ` SmCl3 and DyCl3 in alkali chloride baths has been investigated in NaCl, KCI and eutectic LiCI- KCI by means of electrochemical transient methods. The thermodynamic behaviors of rare-earth containing species have been discussed in the frame of Electrode potential - P02- diagram. Low current efficiency found in the case of Nd electro-winning has been attributed to the dissolution of Nd into the bath. The analyses of electrochemical measurement required the elucidation of the effects of the factors such as under-potential deposition, metal dissolution, moisture and oxygen partial pressure.

Jan 1, 2003

In accordance with the new concept described in the paper presented at the TMS annual meeting in 1989, 1 a new zinc cellhouse was constructed and successfully operated. The new concept was proposed in order to reduce energy requirements and to mechanize the electrode handling in the cellhouse. Major modifications involved the use of an electrode unit consistfog of assembled anodes and cathodes with frame bodies between each cathode and anode. The space between a cathode and an anode could be halved by this unit structure. In this paper actual operation data are summarized and discussed in comparison with the calculated figures.

Jan 1, 1990

By José Luiz Rodrigues Bravo

The production of electrolytic copper with assured quality corresponding to international standards, in a conventional electrorefkery of a custom smelter, is a hard and cautious task, if no advanced technologies for selective control of electrolyte impurities are available. The improper control of the amount of As , Sb and Bi in the anode that enter the tankhouse , attributable either to a bad schedule of concentrate input or to the unavailability of clean concentrates in the international market , as well as the lack of means to maintain the suitable level of these elements in the electrolyte together with other operational circumstances, can result in off-grade copper, as well as affect the starting sheet chemically and physically. This paper presents in a practical way the relationship between the operational conditions and the cathode and starting sheet quality produced at CMSA, covering the period of the last five years of operation, discusses the technologies available in the market for antimony and bismuth removal and compare the results of testwork, achieved in the laboratories of CMSA, using two resins not associated with patented technologies.

Jan 1, 1997

By M. Misra, J. Nanor

The precipitation and removal of arsenic from process waters can be accomplished with addition of lanthanum chloride alone or in conjunction with ferric sulfate. The long term stability of these corresponding precipitated compounds is critical from the disposal stand-point. In this paper the characterization of ferric, lanthanum and lanthanum-ferric arsenate compounds formed at room temperature in acidic and alkaline pH is presented. The characterization techniques used included zeta potential, XRD and SEM. Zeta potential measurements of ferric and lanthanum hydroxides in the presence of arsenate indicate that oxyanions of arsenate are chemically adsorbed onto the positively charged surfaces of these hydroxides. In alkaline pH there is desorption of arsenate species from the ferric hydroxide surface, hence the product is thought to be unstable. On the contrary, lanthanum arsenate is stable in alkaline pH. XRD patterns show that the ferric arsenate formed in acidic and alkaline pH is amorphous, whereas lanthanum arsenate and lanthanum-ferric arsenate formed in acidic and alkaline pH are crystalline.

Jan 1, 1999

By Akram Alfantzai, Farzad Mohammadi, Maysam Mohammadi

"Degradation of lead anodes has always been a major concern among the electrowinning industries. In this study, the effect of agitation of the zinc electrowinning solution on the integrity of lead anodes was investigated. Galvanostatic experiments were performed at 37±0.5°C using 0,600 and l000rpm magnetic stirring rates for 24 hours. The Pb02 layer formed on the anode surface was reduced to PbS04 (discharged). The discharge information was used to calculate the amount of Pb02 present on the surface. Weight loss measurements along with the discharge calculations revealed that the degradation rate of the lead anode increased as the solution was stirred more vigorously. Furthermore, the amount of remaining Pb02 on the surfaces was decreased as a function of solution velocity. Therefore, it may be concluded that, degradation rate oflead anodes is controlled by detachment of the corrosion products from the surface rather than by electrochemical reactions. IntroductionElectrowinning is one of the extraction stages of zinc, in which pure zinc is deposited from acidic solution after froth flotation, roasting and leaching processes. The anode electrode materials play important roles in the electrowinning process. Their electrocatalytical capacities determine the oxygen evolution overpotential, and consequently the cell potential and energy efficiency of the zinc electrodeposition [l]. Purity of the zinc deposited on the cathode is affected by the solubility and corrosion resistance of the anode materials. Using insoluble materials as anode in the electrowinning leads to the higher purity of the deposited metal on the cathode[2]. Lead (Pb) and its alloys have been used as the anode in the zinc electrowinning because of its special properties such as relatively low cost, low melting point, insolubility in solutions containing sulphuric acid and high conductivity in both states of metallic and oxidized [3, 4]. In zinc electrowinnig, zinc reduction occurs on the cathode (reaction 1) and the oxygen evolution reaction (OER) (reaction 2) is the main anodic reaction [5, 6]."

Jan 1, 2013

By Jayagopal Ucbil, M. Krishna, V. T. Vijayalakshmi

"The pitting susceptibility of aluminium metal matrix composites reinforced with garnet particles has been examined using static weight loss method by exposing the metal matrix composites (MMC) specimens to the action of IN HCI acid at laboratory temperature for different time intervals. It was found that the corrosion rate decreased with increase in weight percentage of reinforcement while the corrosion rate was a function of the matrix alloy but not of the reinforcement material. Further, it was found that the rate of corrosion was dependent on the interface region formed between the reinforcement and the matrix. A comparison of the base matrix with the corresponding composite when subjected to heat treatment for varying periods of 4, 8, and 12 hours respectively was made. The comparison revealed that corrosion resistance of the composite increased with the duration of heat treatment and this has established a considerable improvement in corrosion resistance of the composite when compared with the base matrix.IntroductionMetal matrix composites (MMCs) offer designers many added benefits, as they are particularly suited for applications requiring good strength at high temperature, good structural rigidity, dimensional stability, and light weight [1-5]. The trend is towards safe usage of the MMC parts in the automobile engine, which work particularly at high temperature and pressure environments [6-7]. Particles reinforced MMCs have been most popular over the last two decades. Among the MMCs, the most popular families are represented by aluminium reinforced with ceramic particles. Although the incorporation of the second phase into a matrix material can enhance the physical and mechanical properties of the base metal, it could also significantly change the corrosion behavior."

Jan 1, 2000

"Depletion of known ore reserves and increased demand for precious metals have caused a revolution in biohydrometallurgical processing technology for gold recovery. Known ore deposits and future discoveries are most likely to be lower grade sulfide ores that can be difficult to recover with current leaching technology. Future metal recovery operations will increasingly use bio-oxidation techniques.Bacteria are an integral part of mineral cycling and mineral transformation in nature. Although biological processes are recognized as part of the mineralization and oxidation reactions in some ore deposits, they have only recently been applied to enhancing metal recovery in hydrometallurgical procedures. This paper explores the traditional metallurgical application of biological leaching and oxidation reactions and reviews the complete range of bacteria available for metal recovery systems. Pre-treatment of ores with bacteria improves metal recoveries in tank leaching systems and shows promise for heap leaching methods.IntroductionThere is no longer any question that bacteria playa natural role in the on-going transformation of some ore deposits (1,2). As applied to sulfide ores, a few strains have been specifically identified that exhibit a natural leaching potential (3). These bacteria can be isolated from waters and soils in old mining districts where they contribute to continuing leaching and pollution problems in acid drainage and heavy metal solubilization. Sulfur and iron bacteria as well as many heterotrophic strains have also been found in ore deposits and sedimentary rocks at depths up to 2000 meters (4). Their presence in both ore deposits and processed ores shows the microbial association with natural leaching and the potential role that bacteria can play in the development of new leaching technology."

Jan 1, 1988

By David B. Dreisinger

Mass and heat balance modeling is a powerful tool for the design and analysis of hydrometallurgical process flowsheets. In this first of two papers, we examine the basic fundamentals of mass and heat balance modeling, and apply these concepts to several flowsheets using a simple spreadsheet model. In this way, we aim to demonstrate how such models are not only easy to construct, but can also be indispensable for comparing various flowsheet alternatives, for making rational economic decisions, and for developing a basic understanding of existing process behaviour.

Jan 1, 2002

By B. Q. Li, R. A. Mirshams

"A numerical algorithm is described for the simultaneous prediction of the thermomechanical behavior of the materials and microstructure evolption during metal forging. The numerical development is based on the finite element solution of the thermoviscoplastic deformation of metals coupled with the internal state variable model describing the microstructure evolution involving work hardening, recovery, recrystallization and grain size distribution. The finite element code for rigid viscoplastic deformation is developed based on the modification of the existing code for the thermal and fluid flow calculations. The code is tested against and compares well with the results reported in literature. The procedures for the integration of the · rnicrostructure model into the macro finite element model are described. Results are presented showing the characteristics of materials dynamics and mechanical deformation during simple metal forging processes.IntroductionIn industrial deformation processes such as hot rolling and forging, the workpiece undergoes both macroscopic plastic deformations and microstructural evolution. A computer model that allows to predict both materials dynamics and macroscopic deformation is obviously more useful for both fundamental understanding and deformation process optimization. For some industrial applications, especially those involving novel, light and high strength materials, such an integrated model is critical in that both materials and thermomechanical 'behavior during forging must be carefully controlled to obtain the products that meet the desired strength requirement [I]."

Jan 1, 2000

By R. Padilla

A thermogravimetric study has been conducted to follow the decomposition and volatilization of arsenic from enargite concentrate in nitrogen and slightly oxidizing atmospheres. Temperature has a large effect on the rate of volatilization of arsenic. Fractional volatilization of arsenic as high as 98% were obtained in less than 60 min at 650°C in nitrogen atmosphere, while in slightly oxidizing atmosphere the same volatilization could be achieved in 30 min. It was found that arsenic volatilizes as sulfide in nitrogen atmosphere and as 4xture of sulfide and oxide in atmospheres containing 1% oxygen. By using the pore blocking and the first order kinetic models, apparent activation energies of 213 and 200 kJ/mol for the temperature range of 780 - 900 K and 205 and 184 kJ/mol for the temperature range of 900 - 985 K were determined for enargite and copper concentrate, respectively.

Jan 1, 1997

By Chen Song

Cobalt basic carbonate particles were precipitated from 1.0mol cobalt nitrate or cobalt sulfate solution with ammonia carbonate. By controlling the zeta-potential of the particles and the ionic strength of the solution, the uniform particles with ellipsoid or rod shapes were obtained. During the precipitation process, the interface tension was diminished to the minimum and therefore the Ostwald ripening and secondary nucleation were both inhibited. The morphology and the size control by zeta-potential seem to be the result of thermodynamics rather than classical crystalline kinetics. The particle sizes were in the range of 0.4-0.6, 0.3-0.4 micrometer. After thermolysis, the spinel-type C0304 particles were produced. The morphologies of C0304 particles were similar to that of their precursors.

Jan 1, 2003

By Jin-tao Gao

In order to recover Ti resource from titanium bearing blast furnace slag, a new technology to separate perovskite phase from CaO-TiO2-SiO2-Al2O3-MgO system by supergravity is researched. In the condition of gravity coefficient of 750g, treatment temperature of 1305°C and time of 20min, the significant layers appear in samples which are obtained by means of centrifugal treatment. Along the direction of the supergravity, the volume fraction of perovskite phase increases gradually, and the equivalent diameters of perovskite phase crystals increases with the area approaching to the bottom of the sample. It is indicated that TiO2 is enriched in the bottom of sample as concentrate with a recovery ratio of 74.05% by supergravity treatment.

Jan 1, 2014

By Omid Marzoughi

In this research, both the kinetics and the mechanisms of the roasting of a sphalerite concentrate from the Bafgh mining complex in Iran were investigated. The oxidation process was performed in a muffle furnace in air and the effects of time and temperature on the degree of oxidation of the zinc sulfide sample were quantitatively studied. The experimental data were fitted to the shrinking core model. In the temperature range of 650–800 °C, the rate-controlling step was the chemical reaction between the zinc sulfide and oxygen with an activation energy of 103 kJ mol−1. On the other hand, in the temperature range of 850–950 °C, the rate-controlling step was oxygen diffusion with an activation energy of 50 kJ mol−1. Also, the roasting process was studied using thermogravimetric (TGA) and derivative thermogravimetric (DTGA) techniques.

By K. Tozwa

The electrical conductivity of electrolytes for copper electrorefining and electrowinning processes has been reported by many researchers since 1911. The experimental results show that the conductivity increases with an increase in sulfuric acid concentration and decreascs with an increase in copper concentration. In pure copper sulfate solution, however, the conductivity increases with an increase in the copper concentration. After confirming the conductivity of pure and acidified copper sulfate solutions experimentally, the concentrations of hydrogen ion and free (not hydrated) water in the electrolytes were estimated and it was found that the relation between the conductivity of acidified copper sulfate electrolytes and the products of concentration of hydrogen ion and free water is linear. Accordingly, the conductivity of acidified copper sulfate electrolytes increases with an increase in sulfuric acid concentration and decreases with an increase in copper concentration.

Jan 1, 2003

By Li Xi

This paper describes how a back-propagation neural network is built for predicting the properties of engineering materials from their other properties, compositions or processes. A predicted result of the impact toughness of a 12Cr-2Ni-1.5Mo stainless steel from its tempering temperature is presented. Furthermore, the combination of this neural network for prediction is able to supplement the unpredictability of the expert system outside its domain of expertise. An integrated system may perform more intelligently and solve more complex problems as well as human expert, in some case even better.

Jan 1, 1992

By Chao Li, Qian Li, Yong-bin Yang, Kai Li, Qiang Xie, Yuan-yuan Zhu, Dong-ye Li, Qi-bing Tan

"The permeability of sintering mix is a vital technological property in sintering process. However, it can only be measured by off-line method on samples picked from the production. In order to acquire the properties of sintering mix accurately, on-line measuring of permeability is urgently required. Based on the reflection characteristics of bed permeability on pipe flowing parameters, a new method is presented in this paper for on-line measuring of sintering mix permeability. The measurement can be performed by blowing gas flow in the bed with the measuring pipe. Measuring results are obtained by picking the data on flowing rate and pressure in the pipe. The function of flowing rate to pressure may be certain for samples with the same permeability. Thus, the permeability was determined by contrasting this function to the result of off-line measuring, and the relative coefficient or R2 value was more than 99%.IntroductionThe permeability of sintering mix is a vital technological property in sintering process, which directly determines production and quality of sinter, or even determines whether the sinter production is carried out smoothly [1,3].The permeability have more obvious influence on vertical sintering speed, which is mainly related to air quantity passing through material bed. Under certain inducing capacity and negative pressure, the vertical sintering speed mainly depends on the permeability of sintering mix. Low permeability may make burning through point of sintering move back, and the sinter mix cannot be burnt through. High permeability may make burning through point of sintering move forward, improving production efficiency by increasing the speed of sintering machine [4] Good permeability means a small resistance of fan ,reduction of negative pressure of sintering machine, and full contact between air and sulfide, which can strengthen physical-chemical reaction during sintering process and increase desulphurization rate. In gas well through material layer process, gas-solid desulfurization reaction and gas-solid-liquid heat exchange are completed and hot gas through the combustion zone supplies the sintering process with heat. Finally uniform sintering of the material layer in height and width direction is achieved [5] While high permeability index leads to weak sinter strength, fast sintering speed, short residence time of high temperature region and little liquid phase. Moreover, liquid phase in the fast cooling process is too late to fully crystallize but forming glass phase which is harmful to sinter strength as well. Bad permeability means a big fan resistance and increase of negative pressure of sintering machine, which make the air pass through material layer difficultly. When air and mix contact difficultly, removal of sulfide reduces so that desulfurization is incomplete. Meanwhile, low caking efficiency, slow sintering speed and easily burnt sinter , reduce sinter output. Therefore appropriate permeability of sintering mix is the premise of stable burning through point and satisfactory sinter output and quality."

Jan 1, 2013