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By Takayoshi Fujii, Mitsumasa Hoshi, Chikashi Suenaga, Yoshiaki Suzuki

"In a bid to renovate its Saganoseki Smelter & Refinery and to establish a leading production unit in terms of global competitiveness, Nippon Mining & Metals undertook major - restructuring efforts since 1993.One of its themes was the shift from a two-flash furnaces operation to a single-flash furnace operation. The shift was successfully completed in 1996 while maintaining the production at the same level (330,000 metric tons per year of copper) by adopting such measures as improvements in pneumatic concentrate dryers, the concentrate feeding system, concentrate burners, the furnace cooling system, and a new cryogenic oxygen plant was constructed.With a view to realizing high matte grade operation (at 65%Cu) and increasing the concentrate feeding rate, further steps were taken the capacity of waste heat boiler was expanded and technical improvements were added, including optimization of the smelting reaction in the furnace shaft. As a result, the smelting capacity, as of the year 2000, has increased to 450,000 metric tons per year of copper.IntroductionThe feed rate to the flash furnace was doubled to 140 t/h from 70 t/h in 1996. Teething problems, as a result of the renovation, were almost solved by the end of 1996, and the operation of the single furnace operation has become stable.The main theme was the shift from a two-flash furnaces operation to a single-furnace operation to maintain the production capacity at the same level, namely 330,000 metric tons of copper per year. Then, in a bid to further renovate the Saganoseki Smelter & Refinery and to establish a leading production unit in terms of global competitiveness, further enhancement of the flash furnace's productivity was planned.The purpose of this plan was to raise the copper production capacity to 450,000 mtpy building on the potentialities of existing plants and without installing new equipment."

Jan 1, 2000

By Wenjie Zhu

Chromite ore processing residue (COPR) is a hazardous waste containing high concentration of chromium. We describe here a pioneer trial of detoxification of COPR in column reactor with an indigenous chromate reducing bacterium Leucobacter sp. Ch1, which showed high chromate reducing ability at high pH. Under the optimum conditions, at 30°C and pH 10.0, pH of leachate decreased from 10.3 to 8.3, and Cr(VI) concentration in solution decreased to zero mg L-1, and 76.4% of Cr(VI) was removed from COPR samples. The leaching toxicity of detoxified residue was 1.1 mg L-1 that was lower than national standard of China.

Jan 1, 2008

By Keizo Uematsu, Satoshi Tanaka, Nozomu Uchida, Ronne Hendrajaya

"The influence of microstructural defects on strength in Si3N4 is reviewed. The presence of cracks, pores and inclusions greatly affects the strength of Si3N4. The micron order crack size and distribution were quantified by micrographic technique. The observed defect size was range from 4 µm to 28 µm.The density of defect increases as the defect size decreases. The correlation between defects size and density was better represented on the logarithmic graph. The correlation was linier. IntroductionFracture in ceramics materials occurs from. In order to understand the relationship between strength and defects, it is necessary to examine the fracture process quantitatively.1In this study, the micrographic technique is used to determine the defects size and distribution in Si3N4. The observed data will be used to predict the material strength by using fracture mechanics rnodel.2Experimental ProcedureThe sintered Si3N4 specimens ( SNl, Japan Fine Ceramics Center) were sliced into 1mm thick . The both sides of specimen surface were polished into by using diamond slurries with particle size down to 2µm. The final thickness was 0.045 mm. The optical microscope (NIKON OPTIPHOT02-POL) was used to observed the internal defects with transmission mode. The reflection mode was used to determine the surface defects, so that the internal defect could be distinguished from surface defect. The measurement and counting was taken on the micrograph and the longest part of the defect was measured as the defect size. The size density distribution of internal defect is taken."

Jan 1, 2000

By Baokuan Li, Qiang Wang, Zhu He

"A mathematical model has been developed to investigate the magnetohydrodynamic (MHD), thermal, and solidified behavior in electroslag remelting process. Based on the finite volume method, a multiphase coupling MHD approach is employed to investigate the droplet formation as well as movement in molten slag under the action of an alternating current. The VOF formulation is adopted for interface tracking. The electrical potential method is adopted for the electric current and magnetic field. The Electromagnetic force and Joule heating are recalculated at each time step and then is implemented in the momentum and energy equations as a source term, respectively. Moreover, solidification of the metal is described by an enthalpy-based formulation, while the mushy zone is treated as a porous medium with porosity equal to the liquid fraction. The model is used to investigate the effect of electrode tip shape on MHD, thermal, and solidified behavior and provide valuable information.IntroductionElectroslag remelting (ESR) process has been used widely to produce high-performance alloys dedicated to critical application, such as hot work tool steels, nickel base alloys, the manufacture of components in aerospace and landbased turbines, etc. Figure 1 shows a schematic diagram of ESR process including a consumable electrode, a molten slag pool, a liquid metal pool, a solidified ingot, and a water-cooled mold. Alternating or direct current flows from the electrode to the water-cooled baseplate through the high resistivity calcium-fluoride-based molten slag which result in Joule heating and Electromagnetic force (EMF). Part of the Joule heating melts the electrode and the droplets travel through the slag and accumulate the liquid metal pool. The electrode is continuously advanced into the slag as it melts to build up an ingot of improved structure and composition by controlled solidification and chemical refinement. The metallurgical properties of the remelted ingot are really related to the solidification structure, which strongly depends on magnetohydrodynamic, thermal, and solidified behavior in the molten slag, liquid metal pool, and mushy zone."

Jan 1, 2014

By Jinfu Xu, Youqing Cao, Yuting Lv, Hang You, Peng Jiang

"In present work, we reported the fabrication of composites consisted of M42 powder metallurgy high speed steel and 45 steel at one step via spark plasma sintering (SPS) technology. The interface microstructure, compositions and microhardness with the interface forming mechanism were investigated. The results show that the morphology and microhardness within the M42/45 steel interfaces exhibit a gradient distribution. The interfaces possessed a transition layer up to 10.2 ?m with few distortions and microcracks. The formation of M42/45 steel interfaces were driven by both fusion and diffusion processes. The former one was primary at the early sintering process, while the later one becomes dominant over the followed sintering process.IntroductionPowder high-speed steels have been widely used in cutting tools, cold-hot tools and dies, as well as in cut materials and structure parts with wear resistance and high-temperature resistance, due to its high hardness, good wear resistance, desirable cutting toughness and favorable hot hardness [1-2]. For materials of some parts in practical production, not only the favorable toughness is required to resist the impact action, but also the high hardness and exceptional wear resistance are demanded. According to the functional requirements and working conditions, bimetal composite materials are prepared in a certain mode, proportion and distribution, by designing two metals with different chemical and physical properties [3-6]. Considering the composites exhibit different properties in different positions of the parts with a combination of the advantages of two metals, they can obtain enhanced properties that the single one can not achieve."

Jan 1, 2012

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 K. Osseo-Asare

Rate laws for the hydrogen reduction of metal ions are typically of the form: [r = -d[M(II)]/dt = k[M(II)]xPy2H] where k is an apparent rate constant, [M(II)] and PH2 represent dissolved metal concentration and hydrogen pressure respectively, while x = 0 - 1 and y = 0.5 - 2. Half-order dependences have been reported for some M(II)/H2 systems; however, no satisfactory explanations have been offered. In an effort to bridge this gap in our understanding, the published precipitation rate data (for M(II) = Cu(II), Ni(II), and Co(II)) are reviewed (with emphasis on the reported reaction orders) and compared with the corresponding but limited electrochemical polarization data. Based on the available literature on the electrochemical kinetics of the M/M(II) and H2/H+ systems it is demonstrated theoretically that, under certain conditions (e.g., in the presence of electron-conducting solids), the rate of the M(II)/H2 reaction can be expressed as: [-d[M2+]/dt = k[M2+]2/1P2/12H] It is concluded that electrochemical processes probably play an important role in the hydrogen reduction of metal ions, especially for systems that involve heterogeneous catalysis.

Jan 1, 2003

By Ray Y. Lin

This study explores the formation of sodium pyrosulfate in molten sodium sulfate resulting from dissolution of SO3 at temperatures between 1160 and 1250 K. Solubility of SO3 in Na2SO4 melts at temperatures between 1160 and 1250 K under gas mixtures of SO2, O2 and argon was investigated applying a thermogravemetric analysis (TGA) technique. The activity of Na2O in the melt was determined with a high temperature electrochemical cell (ECC). Results showed that the SO3 solubility in molten Na2SO4 increases with decreasing temperatures and increasing SO3 partial pressures. Enthalpy of SO3 dissolution in molten Na2SO4 was calculated to be -119 kJ/mol for infinite dilute solutions. Thermochemistry of Na2SO4-Na2S2O7 melts was analyzed based on information obtained from both TGA and ECC techniques. Detailed examinations of the earlier low temperature measurements in the Na2SO4-Na2S2O7 system along with data from this study reveal that the solution behavior between Na2SO4 and Na2S2O7 can be satisfactorily treated as regular with the interaction parameter, , being 2.7 kJ/mol. The phase diagram and the field of SO3 partial pressure has been generated with the thermodynamic calculation using a regular solution approach.

Jan 1, 2006

By Eiichi Kuzuno, Atsushi Shibayama, Toyohisa Fujita, Kazuo Koike, Toshio Miyazaki, Hitoshi Masuda

"A solid sulfur is more useful to recover and store than a sulfuric acid as a by-product in the zinc hydrometallurgy. In this experiment a zin concentrate (sphalerite) was leached with ferric sulfate at about 373 K for 3 to 6 hours. Zinc was leached more than 95%. After a solid-liquid separation, the leached residue contained solid sulfur was obtained. The particles in the residue were dispersed by lignin and the solid sulfur of approximately 85% was recovered as float product by a flotation with frother in the pH 4. The dried float product was heated at 413K for 2 hours. The pure solid sulfur was recovered. On the other hand in the leached liquid a zinc oxide was ·added and ferrous .iron was oxidized to ferric iron by blowing oxygen. This ferric iron was returned to the zinc leached process after solid-liquid separation.IntroductionZinc concentrate is usually roasted as pretreatment in zinc hydrometallurgy and the produced S02 is changed to sulfuric acid. However, recently in Japan the utilization of sulfuric acid has been limited and it is more costly to store. Instead of producing sulfutic acid the solid sulfur recovery has been examined by direct leaching of zinc_ concentrate in this experiment.In the direct leaching, several kinds of effects have been studied for leaching of sphalerite in ferric sulfate solution. The addition of lignine siilfonate1 • 2) and fine· grinding3) increases the · speed arid leaching fraction of sphalerite. The leaching ratio depends on impurities in sphalerite ores4 • 5). Here, the zinc concentrate is leached ferric sulfate solution under atmospheric pressure at 373K. The solid sulfur in leached residue is separated as float products from other solids by sink-float separation and flotation. The sulfur in float products is purified by evaporation at 413K and recovered."

Jan 1, 2000

By Ahmet Geveci

[Generally accepted formula related to sulfur slag-metal distribution ratio is given by the following equation: [ ] According to the above equation it can be deduced that sulfur distribution between slag and metal is governed mainly by metal composition (?s term), slag composition (slag basicity and in turn sulfide capacity), oxygen potential of the system (ao¬¬ term) and temperature(related to equilibrium constant, K). In this study, the results of ladle furnace operations conducted in Erdemir-Iron and Steel Works Co. (Turkey) in relation to sulfur removal, have been given. Typical ladle furnace slag analyses of 4937K quality steel have been presented. Activity coefficient of FetO,?FetO, have been calculated with the relation obtained fromthe literature. Activity calculations have been performed with the program written in Mathcad. The changes in activity of aFetO in the slag phase,, have also been studied in relation to the sulfur removal: The relation between % Decrease aFetO and %DeS (measured)have been investigated for 4937K runs and someother types of steel produced in the Erdemir Plant. Related to ladle operations %desulfurization defined as [(%Sinitial-%Sfinal)/S%initial]*100 values have been presented for different steel qualities.]

Jan 1, 2006

By Nan Zhang, Gai-feng Xue, Shangchao Liu, Benquan Fu

"The high-magnetization microspheres of Fe3O4 encapsulated with S1O2 and T1O2 layers (Fe3O4@SiO2@TiO2) were prepared. The microspheres were characterized by transmission electron microscopy and scanning electron microscopy. These high-magnetization microspheres could be readily dispersed by shaking whereas they could be rapidly separated from the aqueous solution simply by applying an external magnetic field. The two shells of S1O2 and T1O2 protected the iron oxide well and the microspheres were stable in acid and base solutions. Therefore, they have a good potential for the enrichment of phosphopeptides or photocatalytic activity. They could also be used to remove metal ions from waste water.IntroductionSolid-phase extraction (SPE) is the most commonly used separation technique for its simplicity, consumption of small volumes of organic solvent, and the ability to achieve a higher enrichment factor. The quest for new adsorbents is an important factor in improving analytical sensitivity and precision in SPE techniques. To date, many novel adsorbents, such as nanometer-sized materials, carbon nanotubes, mesoporous materials and magnetic nanoparticles have been employed in SPE.Magnetic polymeric microspheres, an interesting advanced composite material, have received increasing attention in the past few decades because of their unique physical and chemical properties and their potential for use in applications in various fields [1]. Magnetic microspheres consisting of an iron oxide core and a silica shell have attracted particular attention for their unique magnetic response, low cytotoxicity, and chemically modifiable surface. The core-shell magnetic silica microspheres have shown great potential in the fields of biotechnology and biomedicine for applications such as cell labeling and separation, enzyme and protein separations, targeted drug delivery, and magnetic ferrofluids hyperthermia."

Jan 1, 2012

By Xiangru Chen, Honggang Zhong, Qijie Zhai, Qingqing Sun

"A horizontal directional solidification equipment, with an in-situ pouring system, was employed to physically simulate the solidification behavior of continuous casting. In this paper, the 2304 duplex stainless steel (DSS 2304) was investigated using this equipment due to its microstructure produced by continuous casting process was usually not satisfied. The grain size combined with the position of columnar to equiaxed transition (CET) of DSS 2304 were observed and the results showed these microstructure characteristics were very close to those of the continuous casting slabs. In addition, the influences of pouring temperatures and cooling conditions on the CET behavior were investigated. The results revealed that the length of the columnar grains decreased with decreasing the pouring temperatures and flow rates of the cooling water. Besides, the content of austenite decreases with increasing the distance from the chilled sidewall.IntroductionDuplex Stainless Steels (DSSs) have been widely used in industry for their excellent mechanical strength and superior corrosion resistance in Cl- environments when compared with other stainless steels [1,2]. Their good performances are mostly on account of the duplex phase structure-ferrite (d) and austenite (?) and the high proportion of alloying elements. Although, DSSs have good ductility, but worse formability compared to the austenitics, and this is the key to restrict DSSs application [3]. This is due to the differences properties between the two phases. The hot workability of ferrite (d) is better than austenite (?) and exhibits a lower flow stress during hot rolling processing [4]. The early workers had revealed that coalescent force of phase interface, microstructure, difference of mechanical property between two phases and the precipitations are the main factors affecting the formability of DSSs [5,6]. Another important reason that affects the alloy’s mechanical properties is columnar to equiaxed transition (CET) [7]. It often occurs during continuous casting solidification process and induces inhomogeneous mechanical properties and the microstructure varies with different processing parameters, such as pouring temperatures, cooling conditions (water flow rates in the cooling zones) and casting speed [8]."

Jan 1, 2012

By Vladimir Mindin

Simulation of complex equilibria is usually done in the P-T-X coordinates, where "Xu is the amount of individual chemical components in the system. This approach is not productive in some very important cases: (i) investigation of "open" systems, (ii) determination of coordinates (trajectories) of mono-variant points, among others. To solve these and some other problems, we use the idea of chemical potentials of elements (CPE) of the system. A system of different coordinates axes (CPE-axes ) leads to a new strategy of simulation, observing the results of the simulation, and to efficient technology of compressing and storage the data of the simulation.

Jan 1, 1994

By Jorge Alberto Soares Tenório, Victor Bridi Telles, Denise Crocce Romano Espinosa, Felipe Fardin Grillo, Vicente de Paulo Ferreira Marques Sobrinho, José Roberto de Oliveira

"This research aims to study the process of incorporation of the metal iron in electric arc furnace dust (EAFD), from a steel mill producing long steel by liquid iron in addition to the changing temperature of 1400 degree Celsius altering experimental conditions such as how to add the EAFD (as received and in the form of briquettes), the percentage of EAFD to be added (10, 20 and 30% of initial weight of sample pig iron) and the time of withdrawal of the sample of pig iron and slag (30 minutes after the addition of EAFD). Previously, the EAFD will be characterized using the following techniques: chemical analysis, particle size analysis, X-ray diffraction, scanning electron microscopy (SEM) and Energy Dispersive Spectroscopy (EDS) microanalysis. After characterization, the eletric arc furnace dust to be added to the bath of liquid iron, will be divided into 2 types: the first order of addition will be in the form ""as received"" from the plant and the second is through the agglomeration of EAFD in the form of briquettes. The achievement of fusion experiments in laboratory scale, will take place in a vertical tubular furnace with temperature control. The fusion experiments to assess the incorporation of the metal iron will use graphite crucibles. A flow of inert gas (argon) will be maintained inside the furnace during the experiments. It is expected that the results obtained at the end of the research allow the evaluation of the iron metal incorporation of eletric arc furnace dust in hot metal bath.IntroductionThe steel industry generates a variety of solid wastes, liquid effluents and gaseous emissions at various stages of processing. The electric furnace dust (EAFD), generated in electric arc furnaces, represents a major problem for their content of chemical elements such as zinc, iron, chromium, cadmium, among others, issued to the atmosphere during the manufacture of steel[1]."

Jan 1, 2012

By C. E. Abbey

Cobalt, iron and manganese play various roles in copper electrowinning using lead–calcium–tin alloyed anodes. Cobalt catalyzes electrochemical water decomposition resulting in lower anode potential and reduced corrosion rates. Iron reduces cathodic current efficiency, but is used to reduce higher oxidation states of manganese that oxidize organics in solvent extraction. Manganese also produces anode scale and is generally considered a problematic impurity. The effect of the combined interaction of these three metal ions on the anode potential has not been quantified yet. The current work used a three factor, two level, three replicate central composite design of experiments to analyze the effects and potential interactions among cobalt, iron and manganese. The experiments consisted of chronopotentiometric analysis to assess anode potential after 24 h of operation. Higher [Co], lower [Mn] and either high or low [Fe] yielded lower anode potentials. Two regression models were developed to predict anode potential as a function of [Co], [Fe] and [Mn]. A method to estimate electrical energy consumption for copper electrowinning is also presented.

By José C. Escobedo B.

A kinetic study of nitrogen dissolution in a. electromagnetically stirred Co-Cr-Mo alloy bath was made. The experiments were carried out at 1693, 1723 and 1743K of temperature, with a nitrogen pressure of 0.67 atm. The mass transfer coefficients were obtained, finding that their values increase as temperature grows. The true kinetic constants were calculated. It was found that at 1693K of temperature, the kinetics of the nitrogen dissolution process is controlled by a mixed mechanism involving both transport processes and chemical reaction, while at 1723 and 1743K of temperature, the kinetics is controlled only by transport processes mechanisms.

Jan 1, 1995

By Lianjun Liu, Ying Li, Qianyi Zhang

"Photocatalytic reduction of CO2 by H2O for production of Cl fuels (CO and CH4) was studied using copper and iodine co-modified TiO2 (Cu-IffiO2) nanocomposites, with copper deposited on the surface and iodine doped in the lattice. The nanocomposites were prepared via a combined hydrothermal and wet impregnation process. All I-doped samples demonstrated visible light activity. Under UV-vis irradiation, co-modification of Cu and I significantly increased TiO2 photoactivity compared with bare TiO2 or those modified with only one species.IntroductionThe photoreduction of CO2 into fuels on photocatalysts such as TiO2 has been regarded as an important approach to solve both energy shortage and globe warming problems [1]. However, the wide band gap and fast recombination ofphotoinduced hole (h+) and electrons (e"") limited the application of TiO2 in CO2 photoreduction reaction. Extensive research has been conducted to improve the photocatalytic ability ofTiO2 by depositing or doping foreign ions that can enhance charge transfer and/or creates intra-band-gap states to induce visible light absorption at the subband- gap energy. Compared with mono-doping, co-doping of metal/nonmetal species has been reported to have higher photocatalytic activity for TiO2 [1-3]. Our previous studies showed that Cu deposited on TiO2 [4] or iodine doped in TiO2 [5] significantly enhanced the catalytic efficiency for CO2 photoreduction and increased the response to visible light. We hypothesize that there could be a synergetic effect if TiO2 is co-modified by both Cu and I species resulting in further improvement in CO2 reduction efficiency. In this work, we synthesized and characterized Cu-IffiO2 samples and investigated their activity toward CO2 reduction under visible and UV-vis illumination, respectively.Experimental MethodsMaterialsTitanium tetra-isopropoxide (TTIP, 98%) and isopropanol (C3HsO, 99.8%) were purchased from Acros Organic. Iodic acid (HIO3,99.8%) and Copper Chloride (CuCh, 99.9%) were purchased from Alfa Aesar. All other chemicals were analytical grade and used without further treatment."

Jan 1, 2012

By Isıl Kerti, Sibel Daglılar, Sinem Yıldırım

In this study, effect of rolling and coiling temperature in thermo mechanical controlled process (TMCP), on the microstructure and mechanical properties of dual phase (DP) steel according to martensite volume fraction (MVF) rate was investigated. By using various finishing mill exit temperature and cooling conditions that is controlled laminar cooling system, the microstructural evolution of coil improves the mechanical properties with lower costs and higher productivities, in comparison to the heat treatment after rolling. The main part of the paper contains the result of tensile, yield and microstructure properties of DP600 steel produced on hot strip rolling plant and run- out table line. The results show that a higher MVF and an increasing cooling rate after the last deformation raised strength of the DP600 steel. The yield strength and ultimate tensile strength increase by decreasing coiling temperature.

Jan 1, 2015

By Niels Verbaan, Ralph Fitch, Charlotte Forstner, David Dreisinger

A process has been developed to extract gold, silver, indium, gallium, lead, copper, zinc, and other metals from a large resource using an oxidizing acid chloride heap leaching technology. The ore is crushed and/or ground to improve reactivity and then contacted with a solution containing NaCl-HCl-NaOCl. The value metals are leached into solution as chloro-complexes. The leachate is treated in a series of separation and recovery processes to produce separate saleable or disposable products. The paper will provide a summary of process development and application to a silver-indium ore from Bolivia. The possible application of the process to other ore types will be presented for discussion.

Jan 1, 2015

By Nelson Collao I.

Loss of the organic phase from solvent extraction circuits is a major cost factor for SXEW operations. Recognized sources of loss include evaporation, entrainment, and biological degradation. The mechanisms for both entrainment and evaporative losses are well recognized. Biological degradation of the organic has not been as extensively evaluated as the other mechanisms but is a major source of loss. This paper discusses the impact of biological degradation on an operating plant, potential mechanisms for degradation, conditions under which biodegradation of plant organic can occur and plant conditions that may assist in promoting biodegradation.

Jan 1, 2003