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By Florian Kongoli

The liquidus surface of multicomponent slags is an important parameter in various smelting and converting processes. It helps not only to optimize the slag, chemistry of current processes and their fluxing strategies, but also to determine the availability of new slags for more advanced technologies. In a series of our previous publications, the liquidus surface of some multicomponent iron oxide slags has been quantified at several constant oxygen potentials and the effect of the latter, ignored until that moment, was quantified along with the effect of some minor components. In this work, the liquidus surface of some iron oxide slags is quantified at constant CO2/CO ratios. This is a new convenient way for the quantitative description of the slag liquidus surface and the effect of several fluxes, especially in those processes such as slag solidification, where oxygen potential changes continuously. This type of diagram also describes more dynamically the effect of oxygen potential, clarifies the relation between CO2/CO ratio and oxygen potential in terms of the liquidus surface, which is not widely understood by metallurgist today, and reduces the gap between laboratory work and industrial experience.

Jan 1, 2002

By N. E. Ablesimov

Electron probe X-ray microanalyser of a coating deposited with "Elitron¬22A" electrospark alloying (ESA) set (anode - Cr, base-catode - chrome vanadium steel) has shown that the zone of phase forming can be divided into three parts: the coating itself, diffusion zone and a thermal affection zone in the base material. Waves of iron and chrome concentrations have been found in the diffusion zone. The authors interprete them as a phenomenon of substance self-organizing in the 30 pill deep diffusion zone, characterized by a change of compositions during the transfer of material from the coating to the base: coating - 20 µm (FeCr2), diffusion zone - 30 µm (Fe3Cr, FeCr, Fe4Cr, Fe2Cr), base - steel (Fe - 87 %, Cr - 12 %, V - I %). This ESA phenomen has been noted for the first time. It may be relative to the phenomenon of periodic formation of secondary products during the mutual diffusion of reacting substances in the case of a one-way reaction. Similar regular structures may appear in the diffusion zone during ESA of vanadium steels with vanadium, manganese steels with manganese and so on.

Jan 1, 1999

By Hector M. Henao

There is an increasing trend in the copper smelters to recycle electronic materials, which contain relatively high concentration of precious metals. As a consequence, the amount of precious metals lost in the slag phase is increasing. To determine the portion of the precious metals chemically dissolved and that associated with the mechanically trapped matte in the slag will be a key factor to improve the recovery of those metals. Thus, an experimental study was carried out to determine the distribution of precious metals (Au, Pt, Pd, Rh, Ru) between the equilibrated copper matte and iron-silicate slag phases. The experiments were made in a magnesia crucible at 1573 K and a fixed partial pressure of SO2 of 0.1 atm for the matte grades between 40 and 70 mass% of copper. It was found that the distribution ratios (defined as mass% X in slag/mass% X in matte, where X represents the precious metal) are around 10-2 for Ru, 10-3 for Au, Pt and Pd and 10-4 for Rh. The distribution ratios show a tendency to increase when the grade of matte is increased.

Jan 1, 2006

By H. Hirayama, T. Okura, O. Kato

"Saganoseki Smelter & Refinery, one of the largest copper smelters in the world, has the annual capacity of 300,000 metric tons in copper content with two flash furnaces, six Pierce-Smith type converters, two anode furnaces, four acid plants, three tank houses and perfect pollution control system.Coping with the many severe conditions surrounding the copper industry in the last decade, Saganoseki Smelter has kept performing the stable operation, while enhancing the smelting capacity and developing new technologies such as the hydrometallurgical treating of converter dust recovered at electric precipitators. Especially in the operation of flash furnaces, which are of Nippon Mining's conversion type using hot air in a temperature of l,000ºC some technological improvements and complete operation control factors have approved the concentrate feed rate to reach to 2,200 tons a day for a flash furnace.Reported in this paper are the production control design for copper smelting process, and the operation control scheme of the flash furnace following the brief review of the characteristic of Saganoseki Smelter's process and some improvements. Copper Smelting ProcessDescriptions of major unit operations and general specifications of the copper smelting facilities are summarized in Table 1, and the present flowsheet of the copper smelting is described in Figure 1 (1,2).Outputs and raw materials treated in the last five years are shown in Table 2, in which concentrate includes powder copper scrap which amounts to 3 to 4% of concentrate.A full operation was performed for a period of one month, for both one flash furnace operation and for two flash furnace operation. With one furnace operation, 19,200 tons of copper were produced. With the two furnace operation, 84,000 tons of concentrates were charged and 33,500 tons of anode (net 28,600 tons of copper) were produced.The actual production level, however, has been kept at 80 to 90% of the full capacity because of low copper price, tight market of copper concentrate or fall of net demand in Japan."

Jan 1, 1989

By Somayeh Dashti, Ehsan Vahidi, Fereshteh Rashchi

"The main goals in zinc electrowinning process are decreasing of power consumption and increasing of current efficiency. In this study, the electrowinning of zinc in the presence of different additives in electrolyte were established and Arabic Gum, Gelatine, sodium lauryl sulphate and l-hexyl-3-methylimidazolium hydrogen sulfate in the five levels using Taguchi method was examined. In our previous researches, using orthogonal array, effect of zinc electrowinning parameters such as anode type, current density, sulphuric acid concentration, temperature and zinc ion concentration was studied and the optimized conditions for zinc electrowinning was obtained. Anode composition: Pb-Ag 0.5%-Sn2%-Sb1%, current density (A/m2):500, acid concentration (g/1):165, temperature: 60°C, zinc ion concentration (g/1):70. The main goals in zinc electrowinning process are decreasing of power consumption and increasing of current efficiency. ln this research, the effect of four additives: Gum Arabic, Gelatine, sodium lauryl sulphate and an organic material in the four levels with Taguchi method was examined. ln fact the effect of electrolyte environment and determining the best electrolyte under the optimized conditions is the main aim of this study.IntroductionDue to its low cost and abundance, zinc is widely used in the production of brass, galvanized steel, sacrificed anodes and primary and secondary batteries [I]. Some 80% of world primary zinc production is derived via roast-leach-electrowinning processes [2-4]. In the electrowinning process to both improve final product quality and current efficiency the leachate should be purified [5].To produce zinc a current method is to extractit from acidic zinc sulphate solutions by electrolysis with aluminum cathodes and insoluble lead-based anodes [6]. Though the electrolytic processing of zinc has been performed for many years, there are still current efficiency problems in the cathodic process. These low efficiencies (88- 93%) have a serious impact on the costs associated with the energy consumption. On the other hand, these low efficiencies increase energy consumption and decrease the quality of the surface morphology [7- 8]."

Jan 1, 2012

By J. Vander Linden, R. De Ketelaere, M. Verhaege

In this paper, results are presented concerning the search to implement Supported Liquid Membrane (SLM) technology for the recovery of copper from electroplating effluents. Acid copper electroplating rinse solutions or effluents resulting from the post-treatment of, for example, cyanide-containing copper electroplating baths all contain copper (2+) in the lower concentration levels. A thorough study of the influence of the individual parameters and of their combined impact on mass transfer in small scale laboratory SLM modules has been performed, enabling to set forward the appropriate operating conditions for a pilot plant installation. The pilot plant, containing two SLM modules. of 18 m2 of surface area, has been tested extensively, including short and long term runs, with real process solutions. It was demonstrated that this installation is able to treat 40 l/h of acid copper sulphate rinse solutions· containing 500 ppm of copper. The final copper concentration in the effluent can be reduced to a few ppm while copper metal is recovered by electrolysis of the concentrate. This technology is also applicable to the treatment of solutions with low copper content of origins other than plating shops, such as tailings from copper plants or mine waters.

Jan 1, 2000

By Manolete Mena

WC-Co nanocomposite powder is among the first group of materials with a promising potential for nanocrystalline-materials application. A chemical vapor synthesis (CVS) process that has previously been used for preparing the aluminides of titanium and nickel, and other metallic and intermetallic powders has been applied to the preparation of WC-Co nanocomposite powder. This CVS system was designed so that a tungsten precursor (WCl6 powder) and a cobalt precursor (CoCl2 powder) were separately fed into each evaporator in a reactor by means of specially designed powder feeders. The reduction and carburization of the vaporized chlorides by methane-hydrogen mixtures produced nanosized WC and Co composite powder. The product is a very uniform mixture of the constituent powders, which is important to ensure a high quality of the bulk cemented tungsten carbide product after consolidation. In the present work, the effects of reaction temperature, CH4 to WCl6 ratio, CH4 to H2 ratio, residence time, and Co content on the powder composition and particle size were determined. The products were characterized using XRD, carbon analyzer, and TEM.

Jan 1, 2006

By A. V. Tarasov

Emission of sulfur-containing gases causes most adverse impact on the natural environment in the process of nonferrous metals production. Under the conditions of Arctic regions, in particular in the region of the Norilsk Mining and Metallurgical Complex (Russia), this problem requires a special approach taking into account potential economic and socioeconomic consequences. By reducing the iron sulfide content of flotation concentrates by using new flotation reagents inhibiting pyrrhotite flotation and by applying advanced process flowsheets for flotation it is possible to increase the nonferrous metals content of flotation concentrates by 5% or more along with a corresponding reduction in SO2 formation during their subsequent pyrometallurgical processing. The ways used to resolve the environmental problems in the Norilsk region in the process of nickel and copper production, are based on the improvement of methods for elemental sulfur recovery from metallurgical off-gas by non-conventional techniques, the sulfur recovery from metallurgical gases by production of liquid sulfur dioxide and the technology for pyrometallurgical treatment of sulfide concentrates without SO2 formation. Another opportunity is the development and commercial introduction of hydrometallurgical technologies for treating copper-nickel sulfide ores.

Jan 1, 2006

By Shaohua Ju, Huang Chang-yuan, Lu Shuaidan, Peng Jin-hui, Wu Guoqin, Yaqian Wei, Zhang Li-bo

"The contrastive studies of microwave and conventional roasting copper residue from zinc hydrometallurgical was carried. The experimental results showed that the microwave roasting has the higher dechlorination rate in the same condition such as temperature, heat preservation time and atmosphere. When the samples with 100 mesh grain size, the Cl content turned from 14.27% to 1.33% and the dechlorination rate achieved over 90% at 400°C with 2h microwave roasting. And in the same conditions, the materials' dechlorination rate after conventional roasting just reached around 78%. The phase changes of the roasting process was investigated with X-ray diffraction analysis.IntroductionCl element can be accumulated gradually in the solution of Zinc hydrometallurgical system. When Cl content in electrolysis solution comes up to 100 mg/L, the stability of electrodeposits process would be severely affected [ 1]. It would not only accelerate the consumption of cathode and anode plate, elevate the power consumption, but also cause serious corrosion of device, increase production costs and lower the quality of electrolytic zinc [2]. Thus, C1- contained in the solution should be removed before electrodeposits."

Jan 1, 2013

By Celaletdin Ergun, Ibrahim Erden, Gurbuz Gunes, Thomas J. Webste, Huinan Liu, Abdurrahman Bahadll

"B, Ti, Ag, AI and Cu substituted hydroxyl apatites were synthesized via precipitation method. Then the samples were air-sintered at 1300°C for 2 hrs and characterized with XRD, SEM, FTIR, and cell adhesion behaviors.IntroductionSynthetic hydroxylapatite (HA, Ca10(P04)6(0H)2) has a similar composition and structure to biological apatite. Therefore, it has been safely and extensively used as an implant material for bone substitute. However, synthetic HA has been used for a various applications including medical or non-medical applications, such as matrices for drug release control, bone cements, tooth paste additive, blood purification agent, monolithic implants or coatings on metallic implants, packing media for column chromatography, gas sensors, catalysis and host materials for lasers and luminescent materials, etc. [1-9].The major factors affecting the performance of HA on these applications are crystal morphology, density, porosity, pore size and distribution, chemical composition, and surface structure. As provided by the high flexibility of the apatite structure a great variety of cationic and anionic species can be substituted into HA structure which is specifically considered as an effective method to modify the properties of HA [10,11]."

Jan 1, 2012

By S. K. Kawatra

A growing concern for pyrometallurgical operations is the generation of airborne particulates. These particulates can be generated by combustion processes, or by materials handling. Regulation of these particles by the EPA has become progressively more stringent, first for particulates finer than 10 micrometers (PM10), which are particles fine enough to be inhaled into the lungs. Then, restrictions were introduced on emissions of particles finer than 2.5 micrometers (PM2.5), which are fine enough to become embedded in lung tissues. The next stage of regulations is likely to be ?nanoparticulates,? particles finer than 100 nanometers, which are in a size range where their very high surface area leads to enhanced reactivity. While all of the health effects due to nanoparticulates have not yet been determined, there have been enough studies to indicate that there is a problem, and restrictions on nanoparticulate emissions are only a matter of time. In this paper, it will be demonstrated that dry handling, comminution, and combustion sources represent a significant concern for both PM and nanoparticulate emissions. In regards to dry handling, the effects of utilizing effective dust suppressants on PM and nanoparticulate emissions will be explored.

Jan 1, 2006

Most of the world's zinc metal is produced via the roast- leach-electrowinning (RLE) process. The process is well established, but most of the sulphur in the sphalerite concentrates reports in the acid, which has to be stored and/or sold. There are significant incentives to develop a simpler process with much reduced acid generation. Ferric ion is a well known oxidant for most sulphides, in particular sphalerite, and it converts the sulphide to elemental sulphur. Based on stoichiometry, however, the amount of ferric ion needed to achieve acceptable zinc extractions is prohibitive for downstream zinc recovery from the leach solutions. The process suggested here makes use of less-than-stoichiometric ferric sulphate additions because the ferric ion is regenerated by sparging SO2/O2 mixtures. This regeneration can be effected in-situ in the leach vessel or outside the leach vessel. An example of the application of this new process is presented for a Canadian sphalerite concentrate assaying 60% Zn. The effects of temperature, ferric concentration and ferric ion regeneration are presented. Options to recover zinc from the leach solution are also briefly discussed.

Jan 1, 2000

By P. Hanniala, J. Sulanto

"The requirement for the reduction of sulphur dioxide emissions from copper smelters is becoming more and more important. Therefore, the most important question in smelting technology will be how to produce even, high strength SO2 gas in smelter and how to combine smelting and converting. The best sorution in certain cases is to eliminate converters totally.Outokumpu is already responding to this challenge. As a result of extensive research work, Outokumpu Oy has developed the Flash Smelting Process for direct smelting of blister copper from concentrates in one step.The newest process development is the Kennecott-Outokumpu Flash Converting process, where solidified copper matte is converted into blister copper. The production of low volume high SO2 content gases, separation of smelting and converting operations to allow increased on-line availability, and simplified process control are the major benefits of the process which translates to reduced smelter capital and operating costs.Also, it has been studied the use of the same Outokumpu furnace for smelting and converting alternately when the production capacity is low.In this paper, the developments and improvements of the Outokumpu Process are described from the operation and investment cost standpoints"

Jan 1, 1988

By W. G. Davenport

Most pre-t 988 Outokumpu flash furnaces were built with blast heaters. Many continue to use them. Blast temperatures in these smelters· are typically 400 to 700 K (Table 2. 1) This chapter: (a) shows how hot blast is included in our calculations (b) evaluates the effects orhot blast onauthothermal65% Cu matte production.

Jan 1, 2001

By T. I. Arbuzova

The present work presents the original data concerning using a high pressure torsion method and a shock wave loading technique to produce compact oxide nanomaterials and investigations of the effect of severe plastic deformation on a microstructure, crystal lattice and stability of these compounds. This allowed us to compare two ways of deformation action that can be characterized as quasi-static and dynamic effect, correspondingly. Particular attention was paid to a stoichiometry and surface composition changes upon severe plastic deformations. A procedure for studying chemistry of the oxide nanomaterials by means of nuclear microanalysis and Rutherford back scattering has been worked through. For surface studies the X-ray photoelectron spectroscopy has been used. It was shown that both distortion methods permit to produce massive nano-scale oxide materials from the coarse-grained powder during a single technological cycle. Bulk nanocrystalline materials based on LaMnO3, TiOy and ZrO2:Y2O3 were obtained by the quasi-static deformation technique. Nanoscaled ceramics of CuO, Mn3O4 and LaMnO3 were produced by the dynamic deformations. The density of the nanoceramics comes to 99%. Size effects and specific imperfection of the nanoceramics obtained lead to a set of particularities of physical properties.

Jan 1, 2006

By Zhong g. Shui-ping

A new type Pb-Ag (0.8wt%)-Bi (0~5.0wt %) alloy used as anode in electrowinning of zinc from sulphuric acid electrolytes was prepared. The electrochemical properties of this ternary lead alloys have been tested and compared with those of Pb-Ag (0.8wt %) anodes used in industry. Results show the anodic overpotential decreases with the increasing of Bi content in the alloys. When the content of Bi was 1.0 wt% and 5.0 wt%, the anodic overpotential is about 40?50 mV and 60?80 mV lower than that of Pb-Ag (0.8wt %) alloy, respectively. The formation of oxide layers on the surface of these alloys was traced by LSV methods and the composition of the anodic oxide layers was characterized by XRD and SEM analysis. The surface layer on the two type anodes examined is mainly composed of a?PbO2 and ß?PbO2. But different structure of the surface layer was observed, Pb-Ag (0.8wt%)-Bi (1.0wt %) has a more fine-grained structure as compared to Pb-Ag (0.8wt %). But the film on Pb-Ag (0.8wt%)-Bi (3.0wt %) alloy is rather friable, cracked and not tightly attached to the anode.

Jan 1, 2008

By Renaud Metz

The DOPA process (Direct Oxidation of a Precursor Alloy) was used to prepare ceramic powders based on doped SnO2 and ZnO. The DOPA process consists essentially in the direct oxidation of a homogeneous precursor alloy. A unique advantage of this process is its rather benign environmental impact since no dangerous reactants are used and no harmful by-products are generated. Only oxygen and the alloy metals participate on the chemical reaction to produce the multi-component oxide. Homogeneous alloys of niobium, cobalt and chromium doped tin have been prepared. The molten metal alloy is atomised in air using a double fluid nozzle to produce metallic powders. A subsequent thermal treatment is carried out to fully oxidise the sprayed metal alloy powders. These raw powders are used to prepare a ceramic powder through a mill homogenisation and atomisation process. The ceramic powder is then uniaxially compacted in disc shape and sintered in an oxidising atmosphere. The resulting sintered bodies are metallised on their flat faces and the cylindrical surface is passivated using lead free glass enamel. These ceramics present excellent semiconducting properties with non-linear (non-ohmic) characteristics. The DOPA process is found to be an attractive procedure to obtain ceramic powders for the preparation of SnO2 varistors.

Jan 1, 2006

By David G. Dixon, Ahmad Ghahremaninezhad, Edouard Asselin

"In this study pertaining to the electrochemistry of chalcopyrite, the active/passive behavior of a chalcopyrite electrode in 0.5M sulfuric acid solution was investigated. Potentiostatic and potentiodynamic polarization and multi-cyclic voltanunetry were conducted to analyze the electrodissolution parameters of the electrode.The potentiodynamic and potentiostatic polarizations of chalcopyrite revealed the formation of a passive film on the surface of chalcopyrite. From the potentiostatic study in the passive potential region, a decrease in the dissolution current density by increasing the potential was observed. From this, it was concluded that the passive film is an n-type semiconductor and cation interstitial defects or anion vacancies are the charge carriers. From multi-cyclic voltammetry studies, four cathodic peaks at - 0.37, 0.30, -0.10 and-0.20 YsHE were detected on the surface of a passivated chalcopyrite electrode. The cathodic peaks at 0.37 and 0.30 V were connected to ferric to ferrous reduction and copper sulfide formation, respectively. The peaks at -0.10 and - 0.20 were related to chalcopyrite reduction. The products of the chalcopyrite reduction reactions were suggested to be Cu2S, Cu9fesS16 and Cu5feS4 and evolution of hydrogen sulfide gas (H2S).IntroductionChalcopyrite is the most abundant copper bearing mineral in the world and its dissolution behavior represents the most important technological consideration in the hydrometallurgical extraction of copper [I]. Since the current pyrometallurgical methods for copper extraction from chalcopyrite have environmental issues, many studies have considered the leaching and dissolution of CuFeS2 in different aqueous media [2-5]. The main problem associated with leaching processes is the slow dissolution rate of the mineral [6]. During the dissolution process, increasing the potential of the chalcopyrite in the anodic direction will cause the formation of surface layers which hinder the dissolution rate of the mineral [7]. The precise composition of the layers is in dispute. Previous studies have concluded that these layers could be sulfur [8-9], precipitated iron compounds [8], a solid electrolyte interphase (SEI) - which slows the rate of electron transfer- [10], a metal deficient sulfide [ll], or polysulfidic in nature [12-13]. In order to increase the leaching kinetics of chalcopyrite, the characterization of the layers formed during dissolution is essential and electrochemical methods are important to this end. Studies by Biegler [14] show nucleation and growth of a thin two-dimensional sulfide phase on the surface of chalcopyrite during the exposure of a polished sample in HzS04 solution or air. More studies by Biegler and Swift [15] have shown evidence for nucleation and growth of a 3-dimensional phase at low anodic potentials (around 200 mV vs. OCP). The current-time behavior of the dissolution process in this potential area has the characteristics of expansion and overlap of localized dissolution centers."

Jan 1, 2012

By Marco A. S. Aguiar, Luis G. S. Sobral, Vânia Mori, Paulo A. Medeiros da Silva

"Copper occurs in the crust of the earth, predominantly, as sulphides. Among the copper sulphide minerals, the chalcopyrite is the most abundant and the most refractory to the conventional oxidative processes. This work aims at developing an electrolytic process for treating a copper sulphides flotation concentrate, more precisely chalcopyrite (CuFeS2) and bornite (Cu5FeS4) in the percentages of 70 and 30%, respectively.This paper presents a low-cost operational electroleaching process for treating copper sulphides flotation concentrates, with a high chalcopyrite content. This research practical work aims at improving the copper extraction from that sulphide mineral, in a relatively short time with low-operating cost taking into consideration the influence of a cationic surfactant. The electrolyte of the electrolytic reaction system was a 2,0 mol.L-1 NaCl solution containing CTAB, a cationic surfactant. The electroleaching system contains one DSATM (dimensionally stable anode) anode and two nickel or copper foams (threedimension electrodes. During the electroleaching process the chloride ions are oxidized to chlorine at the anode surface, which in contact with the aqueous phase generate enough hypochlorite ions to oxidize chalcopyrite.The copper ions released from the chemical oxidation process are reduced at the cathode surface as metallic copper."

Jan 1, 2008

By Wenshan Zhang

The industrial production experiments on Zn, Mn simultaneous leaching, impurity removal and ZnMnO2 simultaneous electrolysis were carried out. The process flow, technical requirement and research results about the experiments were discussed and the good technical quail-fixation and high quality of products were obtained. Reactions for each major technological process have been expatiated based on the thermodynamic analysis.

Jan 1, 2006