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By Xiao Long, Ting Wu, Lilong Zhu, Qian Wang, Shengping He

"During the continuous casting of peritectic steel slabs, mould fluxes with high crystallization capacity are usually chosen for improving slab surface quality. However, the lubrication condition of casting shell also could be deteriorated. Since precipitation of crystals within liquid slag film can change the composition and property of liquid slag over solid-liquid slag film interface region, its impacts on continuous casting process also are not clear. In order to clear this phenomenon, an experiment method was put forward, and mould fluxes for peritectic steel slabs continuous casting were selected and examined. The results reveal that after crystals have been separated, the crystallization capacity of leftover liquid slag increased with different levels, which could deteriorate the lubrication condition of casting shell and cause a series of problems. Thereby, mould fluxes with high crystallization capacity at beginning for heat transfer control and then weaker after crystallization should be considered in the future.IntroductionIn the continuous casting of peritectic steel slabs, contradiction between heat transfer control and slab shell lubrication by mould fluxes has been treated as a key problem for maintaining a smooth manufacturing process [ 1]. Strong and uneven horizontal heat flux over the meniscus region will cause uneven solidification of casting shell, especially for peritectic steel slab with enormous volume change caused by phase transition. All of those could cause surface defects like longitudinal crack [2-4]."

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

By P. Thapliyal

The petroleum refining industry generates over a million tons of spent catalyst per year, containing valuable metals. Currently, these materials are recycled to smelting furnaces, but the fundamental mechanisms controlling the recovery processes are poorly understood. Furthermore, submerged injection of finely divided materials is potentially a means to obtain high recoveries of pay metals. In this study, a catalyst containing 10% Ni and 1% Co was injected into 45 kg heats of matte. A copper matte was chosen so that the nickel and cobalt recoveries were measurable. It was found that the recovery ranged from 40 to 700Al, increasing with catalyst feed rate, decreasing with catalyst particle size and decreasing with the oxygen content of the carrier gas. A mathematical model was developed to account for the results, and to permit extrapolation to nickel mattes. The industrial implications are discussed.

Jan 1, 1996

By David C. Lynch

FeCl3 particulate of 10 to 100 um in diameter was reacted with radicals produced in an oxygen plasma at pressures between 1 to 20 Torr. The particulate, in a fluidized bed, was positioned above the plasma to avoid over heating the oxide product which is known to lead to crust and clinker formation[ 1 ]. Reaction between the iron chloride and the gas phase occurred at temperatures between 66 and 226 °C. Oxygen radicals react with the surface material to a depth of approximately 2.5 4m. Surface material, analyzed with a x-ray technique, indicates that the maximum amount of FeCl3 reacted on a weight basis was found to be approximately 67%. More typically, 40 to 50 wt% of the chloride was reacted within 30 minutes to 1 hour.

Jan 1, 1996

By Rikiya Kamezawa, Rudiono, Manabu Takeuchi

"Schottky type solar cells based on phthalocyanine (Pc) thin films were fabricated, and their photovoltaic performance was investigated in various ambient atmospheres. Most of cells prepared in this study showed a good rectification and photovoltaic effects in the visible wavelength region. The introduction ofN02 gas into the measuring chamber was confirmed to increase the current both in dark and under light illumination. However, chemical reaction between the Al electrode and N02 formed some oxide and deteriorated the Schottky barrier, resulting in an increase in cell resistivity. SF 6 gas also showed similar effects on the cell performance.IntroductionPhthalocyanine is one of the typical organic semiconductors, which shows high photoconductive sensitivity in the visible to infrared region. Today, several kinds of metal phthalocyanines are used in electrophotographic photoreceptors. In addition, application of phthalocyanines to solar cells have also been trying by many workers [1, 2]. Many efforts have been made for improving performance of phthalocyanine solar cells by modification of device structure [3, 4], doping by dye or pigment [5, 6] and incorporation of metal clusters [7]. It is known that electrical conductivity in phthalocyanine is increased by adsorption ofNO2 [8, 9]. We tried to improve photovoltaic performance ofphthalocyanine solar cell by adsorption ofNO2. This paper describes the influence of N02 adsorption on the photovoltaic behavior of phthalocyanine solar cells."

Jan 1, 2000

By Dai Xi

In the present work, the viscosities of molten FenO-MgO-Si02 and FenO-MgO-CaO-Si02 semi-synthetic slags for nickel flash smelting were measured in the temperature range from 1473 to 1723K by a rotational viscometer. The ratio of Fe to Si02 was fixed at 1.2, calcium and magnesium oxide contents varied in the range from 2 to 8 mass% and 9 to 12 mass%, respectively. The results showed that silicate anions became smaller by increasing CaO content, which results in a decrease of the viscosity of the slag. In the case of MgO addition the viscosity behavior was complicated. At MgO content below 11 mass%, the viscosity increased with the increase of MgO at all temperatures tested. However, when the MgO content was above II mass%, the viscosity decreased slightly for FenO-MgO-CaO-Si02 system. At higher MgO contents, low-viscosity slags can be obtained by adding CaO. At a given composition, the viscosity decreased with increasing temperature. The higher the temperature, the more MgO can be added before saturation. The effect of Fe304 on the viscosity was quite significant. The viscosity of slag increased by 300mPa's at l573K when Fe304 content varied from 3 to 9 mass%. The viscosity values are presented as the functions of temperature and composition. A comparison between FenO-MgO-Si02 and FenO-MgO-CaO-Si02 systems is given in this study.

Jan 1, 2003

By Yan Fu, Chuanlin Fan, Xiujing Zhai, Yongfeng Chang, Binchuan Li

"The mechanism of the selective chlorination of nickel and cobalt in reduced limonitic laterite was investigated. Reduced ores were obtained from the reduction roasting of a limonitic nickel laterite. The thermal decomposition of related chlorides and the selective chlorination of the reduced ore were carefully studied using Differential Thermal analysis - Thermogravimetry (DTA-TG), X-Ray Diffraction and chemical leaching methods. In the temperature range of 300 - 500 °C, aluminum chloride hexahydrate was chosen as chloride agent. During the selective chlorination, reduced ore was partly chlorinated by hydrogen chloride generated from the thermal decomposition of chloride agent. Then the oxydrolysis of ferrous chloride re-generated hydrogen chloride was used to further the chlorination. Finally, iron was mostly rejected as hematite, while nickel and cobalt were selectively chlorinated. More than 91 %Ni , 90%Co and about 4%Fe in the chlorinated ore was extracted using a water leaching method.IntroductionLimonitic nickel laterite is an important nickel reserve, which is rich in iron in the form of goethite and has low contents of magnesium, aluminum, silicon, and other elements. Goethite is the main nickel-bearing mineral in the laterite [1]. Nickel is generally present in goethite in three modes: (a) associated with amorphous or poorly crystalline goethite, (b) weakly adsorbed to the crystalline goethite surface, and ( c) as lattice substituents [2]. In addition, cobalt in limonite was found to be associated with a manganese phase rich also in nickel [3]. These results indicate that the extractions of nickel and cobalt are highly dependent upon the degree of the decomposition of the nickel, cobalt-bearing minerals.For the selective extraction of nickel and cobalt from limonitic laterite, the ore is usually processed by hydrometallurgical methods, including high pressure acid leaching (HPAL) [4] or reductive roasting - ammonia leaching (Caron process). However, there are still some disadvantages in these processes, such as the expense of autoclaves and scaling problems in HP AL [ 4, 5], and relatively low overall metal recovery, large energy and reagent requirements for the Caron process."

Jan 1, 2011

By Itavahn Alves da Silva, Jose Dimas de Arruda, Amanda Aparecida Fátima Arruda, da Silva de Souza, Carlos Antonio da Silva, Varadarajan Seshadri, Samuel

The knowledge of the flow field inside a continuous casting mold is essential to improve operational efficiency of the process and also to achieve better inclusion control. Physical modeling, PIV technique and CFD have been employed to assess the velocity distribution in the metal- slag interface region in a slab mold. The analysis of results shows how higher casting velocity and lower immersion depth of submerged nozzle can lead to higher turbulence in the slag-metal interface. The effects of density difference between slag and metal and interfacial tension between the phases have been highlighted.

Jan 1, 2016

By Cailing Zhen, Jian Pan, Deqing Zhu, Xianlin Zhou, Yanhong Luo, Guixiang Huang

The grate-kiln process has been widely applied for oxide pellet production with the quick development of steel industry in China, but ring formation takes place which adversely affects the productivity and properties of fired pellets. Rotary kiln at high temperature seems a black box, and ring formation is difficult to measure directly by current technology. It’s of great importance to monitor ring formation during firing of pellets. Therefore, a method for estimating the thickness of ring formation in rotary kilns was studied, based on working out theoretically the relationship between ring thickness and the outside surface of the kiln, according to steady-state heat transfer across a cylinder, which provides a soft-sensing technique for ring formation at high temperature, and achieves stable pellet production .

Jan 1, 2015

By Wolfgang Baum

Case studies from epithermal gold-silver deposits in the western United States and in Latin America show that the routine use of process-related mineralogical studies has become an important tool for the reduction of development, capital and operating costs. Bypassing the mineralogical characteristics of epithermal gold-silver ores, as a result of fast-track development approaches, has resulted in multimillion dollar metal losses and/or in considerable modification costs of existing operations.

Jan 1, 1988

By Andre L. De Vegt

For the past eight years Paques has been engaged in the development and installation of treatment systems based on biotechnological processes to remove sulfur compounds from water, air and gaseous streams. Metal and sulfate can be removed from mine waters using two biological steps: 1. Sulfate reducing bacteria convert sulfate to hydrogen sulfide (HzS). The HzS reacts with the dissolved metals to form insoluble metal sulfide precipitates. 2. Sulfide oxidizing bacteria convert excess H2S to elemental sulfur. Paques has designed and installed a groundwater treatment system for the Budelco zinc refinery in the Netherlands to remove metals and sulfate as described above. The system has been operating since May 1992 treating a flow of 5000 m3/d. A test program, utilizing a large scale pilot plant, will commence in November 1995 at a copper mine in the U.S.A. to remediate groundwater contaminated with sulfate and heavy metals. Biological reactor performance and selective metal recovery will be studied. Sulfur dioxide (S00 can be removed from fluegas using a combination of scrubber technology and the two biological steps. The end product is elemental sulfur. A commercial size biological desulfurization plant has been in operation since July 1994 treating 50,000 Nm3/h of fluegas. Sulfide can be removed from mining waters or anaerobic wetlands using a THIOPAQ® Sulfide Oxidizing reactor.

Jan 1, 1996

By Jiann-Yang Hwang, Ying Qin, Shu-Jing Zhu

Metallurgical Oil Sludge (MOS) is a byproduct created in the process of steelmaking. More than a million tons of MOS are generated each year throughout the world. The material contains hazardous components such as heavy metals and pathogenic organics, which can cause serious environmental problems and health issues. Landfill, combustion, and pyrolysis have been investigated for the disposal of MOS. However, these methods are unsatisfactory since they are unable to reach the clean environment goal. In this study, we investigate the possibility of using MOS as a reductant in a high temperature metallurgical process. The results are reported and discussed.

Jan 1, 2015

By Alexander I. Raitchenko

"An electroconductive viscous liquid may flow in laminar or turbulent regime under Lorentz-force generated by the intercrossed electric current and magnetic field. When there is a starting flat layer between hard and free boundaries with surface tension the spatial Lorentz-force can create a specific stationary regime of flow: the plane free surface will transform into the wavy one, and the movement in the depth will be not laminar and not turbulent, but this regime will be characterized by organized forms with indications of ""rolling of long cylindrical drops"". Wave-length is determined by the viscosity, the density, the surface tension, the average thickness of layer, and Lorentz-force. ·The limit of wavy regime is determined by most long of wave which is directly proportional to the critical value of specific flow and inversely proportional to the kinetic viscosity. The proper critical value of Reynolds number is determined by the dimensionless combination containing surface tension, density, viscosity, and Lorentz-force. The mentioned dimensio.nless combination in our case is some criterion substituting the known Kapitsa number for case of the thin viscous liquid layers under gravity. Spreading of admixture by mechanism of wavy regime is more rapid than by common diffusion or by laminar flow. The suggested conception can be a contribution into the theoretical basis for elaboration of some specific liquid metals technologies."

Jan 1, 1999

By S. S. Ryu, J. C. Kim, H. Lee, Y. D. Kim, I. H. Moon

"Recently, W-Cu alloy becomes one of the very important candidate materials for heat sink and packaging in the field of microelectronics due to its good thermal properties. The metal injection molding of W-Cu powder can satisfy the requirement for mass production of complex shaped parts in microelectronic devices. In the present study, the application of MIM process to the nanostructured W-Cu powder prepared by mechanical alloying was investigated. The multi-component binder system of 45PW+ l 5BW+ 30PE+ I OSA was proven to be suitable one for the MIM of the W-Cu composite powders by adopting the debinding cycles of multi-stage in N2 and H2 atmospheres. Other process conditions for the MIM of the nanostructured W-Cu composite powder were also studied. The MIM debinding part of W-30wt.%Cu was sintered to the relative density of more than 96% by sintering at 1200 °C for !hour in H2 atmosphere. Such an improvement of sinterability was attributed to the intrinsic homogenous and fine mixing state of W-Cu phases in nanostructured W-Cu composite powders, and also partly to the effect of the activated sintering by the presence of impurity introduced during the extensive milling.IntroductionW-Cu alloys have been widely used for heavy duty electrical contacts and arcing resistance electrode(1-2). Recently there has been a growing interest in this W-Cu alloy because of its superior thermal managing properties and its high micro wave absorption capacity(3). Such W-Cu alloy parts are conventionally fabricated either by the Cu infiltration sintering technique or by hot pressing of W-Cu powder mixtures. However, these conventional PM techniques are hardly applicable for mass production of small size parts with a complicated shape such as the parts required for microelectronic devices. The metal injection molding(MIM) technique is potentially applicable for the mass production of small and complicatedly shaped parts compared with other PIM forming techniques."

Jan 1, 1998

By T. T. Natarajan, Nagy EI-Kaddah

"Numerical simulation of electromagnetic confinement systems generally requires large CPU time due to the strong coupling between the electromagnetic and the free boundary problems. The present paper examines the accuracy and the computational efficiency of the most common numerical schemes used in modeling such systems. Levitation melting was taken as a test case. In this study, a comparison was made between the finite element and surface integral methods for electromagnetic field calculations. The computational efficiency of Lagrange and the modified Hestenes methods for solving the free boundary problem were investigated. The convergence of the Lagrange method was found to be much faster than the modified Hestenes method. It was also found that finite element method not only gives accurate solutions, but faster convergence to the final equilibrium shape than the surface integral method. The applications and the limitations of these techniques in modeling electromagnetic confinement systems will be discussed.IntroductionIn recent years there has been a growing interest in the use of electromagnetic forces for confinement of molten metals as a means to eliminate molten metal contamination during melting and to improve surface quality of cast products. Continuous casting of metal without contact of a mold is now a reality, and is being commercially applied for casting of aluminum slabs /1/, and copper rods /2/. New applications of electromagnetic confinement in melting and casting include containerless melting (Magnetic Suspension Melting) /3/, edge containment in twin roll casting, and meniscus shape control in continuous casting of steel /4/.Modeling of confinement systems involves the determination of the electromagnetic field and the equilibrium shape. These two problems are strongly coupled due to the dependence of the field on the shape of the melt. While significant advances have been made in computational electromagnetics /5/, the application of developed computational techniques to electromagnetic confinement problems is not a simple task. The principal difficulty in using these methods is that the solution domain is not known a priori. due to coupling between the electromagnetic field and the free boundary problems. These two problems have to be solved simultaneously, leading to an iterative solution procedure. As a result, numerical simulation of electromagnetic confinement systems are computationally intensive with computational time at least an order of magnitude larger than the fixed domain problems."

Jan 1, 1994

By Christian Redl

"The Lattice Boltzmann Method (LBM) solves fluid dynamics problems based on a discrete mesoscopic approach. It is based on the Lattice Boltzmann equation which is a special discretisation of the continuous Boltzmann equation. Its principle advantage is that it can handle complex physical phenomena (like interaction between different components and surface effects), complicated boundary and initial conditions very well, free from many gridding and stability constraints that plague conventional numerical methods used for fluid flow simulations. Complex structures like porous media can be resolved directly. The LBM algorithm has a simple structure and acts locally, which is favourable for parallel computing. Its potential for metallurgical process simulation is demonstrated in the present study which is concerned with the simulation of the fluid flow in a copper winning electrolysis cell. The electrolyte is modelled as the carrier fluid and the oxygen is considered via a so called active scalar equation. The modelling of buoancy, momentum exchange and the free surface requires special effort. The results of the simulation are validated against experimental data obtained by Laser-Doppler-Anemometry. Despite the simplifications made, good agreement between the simulation and the experiments was found.IntroductionThe hydrodynamics in an electrometallurgical cell is a complex, highly non-linear phenomenon. It includes the simulation of a two component system with high density ratio, gravity driven flow and a free surface. A general solution to this problem is currently unknown.The flow field is a result of the combination of various hydrodynamic effects [18]. Metal deposition at the cathode yields in a decrease in the ion concentration, which reduces the density of the electrolyte. At the anode molecular oxygen is formed as a consequence of the oxidation of water molecules. The oxygen is solved in the electrolyte and again the electrolyte density is decreased. Both effects lead to a free upwards directed convective flow, refered to as natural convection."

Jan 1, 2001

By M. Suzuki, M. Dobashi, M. Kahata, T. Yoshida

Almost 30% of steel in Japan is produced by electric arc furnace (EAF) treatment of iron scrap. EAF dust includes approximately 20 wt % of Zn and 3- 5 wt % of CI and is treated by the pyrometallurgical processes to recover Zn as Zn oxide. Direct hydrometallurgical processing is one of the most effective methods to recover high purity Zn. In this case, CI in the EAF dust is dissolved in the liquid phase by leaching, and the CI anion in electrolyte attacks anodes which are commonly made of a lead base alloy. Several processes have been proposed to remove CI anions from acidic sulfate solution. In this study, an electrolytic process was examined to eliminate CI anions from Zn sulfate electrolyte. From our study it can be said that the elimination rate of CI anion depends on the anode material ( i.e., the elimination rate is Pb-Ag alloy == Pb > DSE== Pt). In industrial Zn electrowinning process, the electrolyte contains Mn, which means the influence of Mn should be considered in the elimination of Cl. Mn dioxide deposition on an anode plate reduces the efficiency of CI removal. A periodical reverse current electrolytic system was examined to prevent this efficiency decrease, and deposited Mn dioxide could be removed very rapidly when the current is reversed. More than 95% of CI anion could be removed by this method in a shorter period than direct current method.

Jan 1, 1997

In the new flowsheet for Inco Limited's S02, Abatement Project at the Copper Cliff, Ontario operations, a copper/nickel sulphide flotation concentrate will be flash smelted, then converted to Bessemer matte. As in current practice, this will be slow-cooled and separated into components by magnetic separation and flotation. The copper content will emerge as a chalcocite concentrate (impure Cu2S), containing some nickel. This copper sulphide will be converted to copper metal.

Jan 1, 1993

By K. S. Kumar

FLS miljø, Inc. markets, designs and supplies particulate collection devices for dusts, fumes, and mists; In this paper, the application of both wet and dry electrostatic precipitators (ESPs) in smelting, and roasting plants is discussed.

Jan 1, 1998

By Ko-ichiro Ohno

It is recently recognized that the iron reduction and melting as well as the slag separation of a composite of granular iron ore and coal are completed in a very short period of about IO minutes when the composite is rapidly heated up to approximately 1673K. These phenomena are expected to be applied to a new iron-making process. The mechanism of iron ore reduction and iron-slag separation during rapid heating has not yet been revealed and the fundamental research has just started. Carburization of the reduced iron is regarded as one of the most important steps in this process. In the present work, the composite was prepared from four kinds of coal or graphite as a carbon source and electrolytic iron powder as a completely reduced iron ore. The temperature at which the liquid formation and iron carburization occurred was monitored. Direct observation of smelting reduction behavior was made by a confocal laser-scanning microscope combined with the infrared image-heating furnace to clarify the effect of molten ash on iron carburization. It was found that the meltdown temperature of composite became lower as the melting temperature of coal ash decreased. From the observed result, it was presumed that the liquid slag would act as an important media for the carbon transfer from coal to iron. The carburization mechanism during the smelting reduction was estimated as follows. When slag containing iron oxide melted down and contacted carbon, iron oxide in the slag was reduced and the formation of the metallic iron particle as well as the its carburization occurred simultaneously at the slag-carbon interface. Carburized iron particle was carried from slag- carbon to slag-iron interfaces due to the slag convection flow caused by the difference of the interfacial tension between the carbon-slag and iron-slag interfaces. Carburization of reduced iron could proceed with a repeat of the above-mentioned process.

Jan 1, 2003