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By K. Pagalthivarthi, P. V. Desai

"During solidification of alloys, many inter-related physical processes, such as melt convection, mass diffusion, heat transport, macrosegregation and melt-undercooling occur. Several research workers have studied one or more of these effects separately. To answer important questions on solidification behavior, an overall approach interrelating the processes is necessaryAs a first step toward accomplishing the overall modeling, the freezing of a binary liquid metal is examined. The various stages during freezing of the alloy are critically described to build a continuum model for the entire process. Diffusive mixture theory is used to write the conservation equations for the liquid and the mushy zones. The concept of local thermodynamic equilibrium in the presence of curvature effects is used to restrict the number of degrees of freedom within the mushy zone. Constitutive equations relating flux quantities and affinities, the governing differential equations and boundary conditions are discussed briefly for the freezing process.IntroductionA solidification study encompasses such facets as solifidication time, microstructure, macrosegregation of the solute, shrinkage effects and soundness of the casting. Influence of one or more of the coupled heat and mass transfer phenomena such as local solute redistribution, thermosolutal convection, melt undercooling at dendrite tips and heat dissipation to the ambient have all been previously examined [1-3J. Several studies have examined the individual facets of alloy solidification as isolated processses. In fact, the transport processes occur simultaneously and a comprehensive model should include their inter-relationships. In particular, some of the existing studies of the mushy zone [4-6J do not emphasize thermodynamic completeness. This work represents an attempt to develop a thermodynamically consistent model of the entire solidification process on physical grounds."

Jan 1, 1986

By Shantaliu S. Shevade, Muhammad M. Rahman

"This paper presents a systematic analysis of fluid flow and heat transfer processes during the magnetic heating of the substrate material. Heat is generated in the substrate material when a magnetic field is imposed due to change in orientation of the molecules. As a result, the substrate temperature rises. The i;tudy considered microchannels with rectangular and square cross section with heat generation in the substrate due to imposed magnetic field. The results computed were for Gadolinium substrate and water as the working fluid. The purpose of this study is to explore the transient heat transfer coefficient when the fluid is circulated through the substrate via microchannels. Equations governing the conservation of mass, momentum, and energy were solved in the fluid region. In the solid region, heat conduction was solved. From the simulation results, plots of Nusselt number and heat transfer coefficient were obtained over the length of the channel. A thorough investigation for velocity and temperature distributions was performed by varying channel aspect ratio, Reynolds number, and heat generation rate in the channel. It was found that the peripheral average heat transfer coefficient and Nusselt number is larger near the entrance and decreases downstream because of the development of the thermal boundary layer. With the increase in Reynolds number, the outlet temperature decreased and the average heat transfer coefficient increased.IntroductionMagnetocaloric effect (MCE) is the heating or cooling of the magnetic materials due to varying magnetic field. The effect was originally discovered by Warburg. Magnetocaloric materials store heat energy in the way the atoms vibrate and in the way electrons spin within each atom. More heat energy increases the vibrations and also makes the spins more random. When a strong magnetic field is applied to a magnetic material, the magnetic moments of its atoms become aligned making the system more ordered. The more ordered material has lower entropy and compensates for the loss by heating up. When the magnetic field is removed, the magnetic moments return to their random directions, entropy increases and the material cools. Gadolinium is a magnetic material that exhibits high temperature rise during adiabatic magnetization around its transition temperature of 295 K. It has been experimentally observed that adiabatic temperature rise increases with magnetic field strength and can be as high 20 K when a magnetic field of IO T is applied. Thus magnetic field, when applied to a microchannel heat exchanger, causes temperature change in the magnetic material. The fluid flowing through the channel gets cooled or heated due to this adiabatic temperature change."

Jan 1, 2004

By Stuart D. Miller, Clayton L. Rumble

"A field net acid generation (NAG) test procedure has been utilized on-site to identify, classify and map potentially acid forming overburden at the PT Kaltim Prima Coal (K.PC) mining operation situated in the tropical equatorial region of East Kalimantan, Indonesia. The field procedure involves routine use of a calibrated, site specific NAG test (rapid oxidation test using hydrogen peroxide) which has a tum-around time of less than 24 hours and requires minimal sample preparation. It is used on geological drill-hole samples, for forward planning and overburden management; blast-hole samples, for day-to-day operational control and overburden scheduling; and final dump surface samples, for verification testing. This operational monitoring program has been in use at KPC for the past four years.Calibration and implementation of the field procedure has involved validating the NAG test using conventional acid-base accounting techniques, producing an overburden geochemical classification scheme, optimizing laboratory and sample preparation procedures, and ongoing quality management. This paper presents background theory and practical application in a case study format."

Jan 1, 1999

By Z. Y. Xie

The visualization techniques were employed for the analysis of computer simulation studies of dislocation core structure in ordered alloys. Atomistic computer simulation was used for the study of the local configuration of the material in the vicinity of the dislocation. Stresses were applied in the simulation in order to study the necessary stress level for the dislocation to move and onset plastic deformation of the material. The results were analyzed in terms of the strain tensor as a function of the position (x, y) in the material with the dislocation located at (0, 0). Various visualization packages are used to plot the invariants of this strain tensor and to visualize the changes that the dislocation core undergoes under stresses until it finally moves.

Jan 1, 1993

By Adam C. Powell

A new Cahn-Hilliard phase field model of transport-limited electrochemistry describes phase boundary motion due to oxidation and reduction reactions at metal-electrolyte interfaces. Benchmarks demonstrating the accuracy of the method include open circuit voltage and closed circuit current in metallothermic reduction, and linear stability theory in metal electrolysis, including a new stability criterion for reduction of liquid metal from liquid electrolyte. The model is applied here to understanding cathode interface stability in titanium electrolysis e.g. in the SOM process developed with Uday Pal, and to structure evolution in subhalide reduction of titanium dichloride by magnesium developed by Toru Okabe. Potential for application to new fuel cell and battery systems is also discussed.

Jan 1, 2006

By Shunhong Huang

To improve understanding the effect of heavy metal chromium on soil biota, laboratory incubation experiment was carried out in the soils contaminated artificially with five concentrations of chromate (50, 250, 500, 1000 and 2000 mg kg_1 soil) over time (35 days). The population and diversity of bacteria, fungi and actinomycetes in soils were measured as indicators of soil microbial processes in the disturbances mentioned above. Incubation experiment results elucidated that the population and diversity of microorganisms decreased with increasing Cr (VI) concentration. Furthermore, various microorganisms showed different sensitivity to total Cr contamination. The sensitivity of microbial population to chromium contamination was in the order: actinomycetes >bacteria>fungi. The resulted implied that the microorganism can be used as an indicator of chromium contamination.

Jan 1, 2008

By Merete Tangstad, Lars Klemet Jakobsson

"Slag refining is a promising refining method for boron removal from silicon as a part of a metallurgical route for production of silicon for solar cells. There is, however, limited data on the distribution of impurity elements between silicon and different types of slags. In the present study, the distribution of boron and calcium between silicon and slag were determined at 1600 °C for calcium silicate slags with a CaO/SiC>2 ratio between 0.65 and 1.3. An almost horizontal linear trend was found for the distribution of boron between silicon and slag, and the borate capacity was found to follow the relationln(CB0, ) = 30.8 + 2.96-V (1)where V\s the CaO/SiCh mass ratio within the range of the experiments.IntroductionSolar grade silicon feedstock contributes significantly to the total cost and energy required to make crystalline silicon solar cells. A less expensive and less energy requiring method of solar grade silicon production is therefore needed in order to make crystalline silicon solar cells more viable as an energy source. Silicon is an abundant element and the manufacturing cost of solar grade silicon is therefore mainly determined by costs related to purification of metallurgical grade silicon. The Siemens process is the most common process today, but it is an expensive and highly energy requiring process that gives silicon with a higher purity than is needed for crystalline silicon solar cells. A cheaper and less energy requiring method for production of solar grade silicon can either be achieved by modifying the Siemens process or by using a new production method. Purification of metallurgical grade silicon through a metallurgical route is a promising method that is already in use industrially. It has however proven to be hard to lower the boron content to 0.3 mg/kg or less, which is the requirement for most p-type crystalline silicon solar cell manufacturers. Slag refining is seen as one of the most promising approaches that can be used to bring down the boron content to the required level, but there is not much data on how boron is distributed between silicon and binary calcium silicate slags [1-4]. The distribution of boron between silicon and calcium silicate slags at 1600 °C has been studied in this work, and the obtained data has been used to calculate the borate capacity of binary calcium silicate slags."

Jan 1, 2012

The concepts of capacity and basicity have proved extremely useful in dealing with a wide range of solute species in metallurgical slags, and as a result have been widely applied. These two concepts are reviewed, and it is suggested that the Lewis approach to basicity has much to commend it. In some cases, it appears that the term capacity has been used without due consideration being given to the nature of the solution being formed, or even to whether a true solution was being formed at all. This paper proposes a rigorous definition of capacity, based on the true nature of the solution process in slags and glasses, and briefly reviews the repercussions of this approach on data available in the literature and the limitations which it may impose on future investigations in this area.

Jan 1, 1994

By Takahiko Okura

"It is said that the energy and resources crisis will come before long because the lifetime of known deposits of crude oil and common metals such as Pb, Zn, Cu is estimated to be less than 50 years. Establishing the sustainable society by means of resources-recycling has become an absolute necessity.The non-ferrous metals industry in Japan has been involved in the resource- recycling business for many years, along with the introduction and enforcement of various legislations to preserve the environment and natural resources. Including process-linkage during various manufacturing activities, the non-ferrous metals industry, the iron-making and cement industries are treating considerable amounts of recycled materials and wastes, in an environmentally-sound and economic manner.The Mining and Materials Processing Institute of Japan has submitted “The present and issues in Japanese non-ferrous metals and recycling industries.”The topic of the paper is to highlight the actual conditions within the resources-recycling structures and the present issues.IntroductionGlobalization has been changing the world, introducing the spike of energy and metals price. In addition, the preservation of the environment has also been strongly facing the crisis and many people have been aggrieved by both shortage and the increment in the price of the meals.In the world of metals, even though their reserves are coming depleted, the production rates are increasing, and then the industry has to enhance their productivity under stricter environmental regulations. The Japanese industry experimented the same scenario some 40 years ago, facing big pollution problems, but concurred them and enhanced the technology to overcome the more severe regulations. It will be fruitful to present the current situation in the Japanese industry for the world. The present issues are also presented."

Jan 1, 2008

By Jack Thibodeau

During the past six years, most states have promulgated water quality regulations which contain numerical aquatic life standards for heavy metals. In addition, the Environmental Protection Agency (EPA) promulgated national water quality standards in 1992 which also include numerical aquatic life criteria for heavy metals. Numerous wastewater discharge permits have been issued by the states and EPA to industrial facilities which include low microgram per liter heavy metal limitations. In many instances, the limitations are below detection limits or treatability limits using state-of-the-art analytical methods or treatment technologies. This paper will discuss options for conducting studies, including the use of water-effect ratios, metal partitioning coefficients, and recalculation procedures to develop site-specific metals criteria and higher permit limitations. The installation of expensive metal treatment systems to remove trace metals may be avoided if higher permit limits are indicated by the site-specific studies.

Jan 1, 1996

By V. M. Mukhin

Among the methods proposed for spent activated carbon regeneration, the most acceptable is, thermal reactivation, because in this case the existing equipment for manufacture of activated carbon can be adapted for this purpose. In order to conduct the process of thermal re-activation of spent activated carbon directly at gold mills, a full-scale drum-type furnace with external electric heating has been developed, i.e. EPV-300 model with a throughput rate of 50 to 120 kg/hour. Its use ensures restoration of the adsorption properties of carbon up to the level of fresh activated carbon with an insignificant (by 0.7%) decrease in strength and with a high (95% to 97%) yield of reactivated carbon. During the recent years, activated powder carbon has been extensively used in flotation processes for treating polymetallic ores at ore treating plants to improve recoveries of main metals (copper, lead, nickel, etc.). Especially large volumes of activated powder carbon are used at the Talnakh concentrator of the Norilsk Mining and Metallurgical Complex in Russia for absorption of residual flotation reagents from recycled water in order to ensure efficient selective separation of minerals with similar physical and chemical properties.

Jan 1, 2006

By F. Guevara

The paper presents results of physical and turbulent three-dimensional numerical simulation of the gas flow in the wind box and reaction shaft of the concentrate burner of a flash furnace. Physical simulation work was carried out in a 1:5 linear scale model, where the velocity field was measured using a Pitot tube. The mathematical model consists of the three-dimensional averaged Navier-Stokes equations, turbulent kinetic energy and dissipation of turbulent kinetic energy using the Renormalization Group (RNG) theory for the k-e turbulence model. Computations were performed using FLUENT, based in a finite- volume code. The geometry of the concentrate burner was separated in two sections: wind box and reaction tower. Results obtained at the exit of the wind box were used as boundary conditions for the reaction shaft. The effect of boundary conditions on the numerical results was also studied. Results of physical and numerical simulations show an asymmetry of the velocity field at the exit of wind box. This asymmetry is possibly due to existence of a separated flow in the back of the exit ring. The agreement of physical and numerical results assess the capacity of the turbulence RNG k-e model to reproduce correctly the behaviour of the velocity field at the exit of the concentrate burner.

Jan 1, 1999

By B. R. Adams

This paper discusses the use of a reacting CFD model to determine chalcopyrite kinetics in a drop tube furnace and to predict the reaction of a chalcopyrite concentrate in the reaction shaft of an industrial smelter. Reacting CFD codes can be applied to determine the consequences of the interaction of gas with particles and therefore improve the ability to derive kinetic parameters that take into account the temperature and oxidation histories that different particles will see. This paper describes the application of such a model to derive improved kinetic parameters for the pyrolysis and oxidation of chalcopyrite. The reaction shaft model includes the effects of turbulent fluid mechanics, entrained flow mixing, turbulent particle dispersion, heterogeneous particle reactions, radiative and convective heat transfer, and' surface and bath deposition rates. Particle reaction and composition characteristics are predicted as a function of particle trajectory and deposition and are used to aid in evaluating shaft performance.

Jan 1, 1999

By Luben Xie, Lin Hu, Qiang Wang, Min Gan, Tao Jiang, Wenqi Li, Yi Wang, Xiaohui Fan

"The mineralization behaviors of typical fluxes are studied by investigating the microstructures with optical microscope. The results show that the reactions begin with between iron ore and lime, limestone with small particle to form primary liquid. Then coarse limestone, dolomite and serpentine take part in reaction under the action of primary liquid. Limestone is the easiest to mineralization, next dolomite, and the last is serpentine. The higher basicity and smaller fluxes size favor the mineralization process of dolomite and serpentine.IntroductionThe purposes of adding fluxes into sintering are that:(1) to increase the basicity of sinter, so as to reduce even eliminate addition fluxes into BF(blast furnace) and decrease the coke ratio of BF[1,2]. (2) to decrease the melting point of sintering mixture to ensure sintering can be carried out at a lower temperature and reduce the energy consumption. (3) to improve the qualities of sinter by forming binding phase with iron ore fines [3].Flux is another significant component for sinter besides iron ore, especially for high basicity sinter[4]. The proportion of flux is usually higher than 10% in sinter mixture(excluding return mine).There were many reports about the influence of the flux types on sintering, such as limestone, dolomite, lime and so on[5-7]. It is very important to choose suitable fluxes for iron ore sintering. Although the effect of flux size on sintering also has been researched, the mineralization behaviors of the fluxes in the sintering process has not been illuminated. The paper will study the mineralization behavior of fluxes in sintering."

Jan 1, 2011

By Qingchun Yu, Bin Yang, Yong Deng, Heng Xiong, Fei Wang, Minxiu Chen

"Metal aluminum produced by non-electrolysis process received much attention due to its lower energy consumption. In this paper, carbothermic reduction and carbothermic-chlorination of alumina in normal pressure and vacuum were studied. The products were examined by means of XRD, EDS and SEM. During the carbothermic reduction process using carbon reductant in normal pressure, no metal aluminum was found. However, when coal was used as reductant, a mixture containing metallic aluminum, A14C3, and silicon was obtained, but metallic aluminum couldn't be separated from the mixture. During the carbothermic-chlorination process in vacuum, Al404C and Al4C3 were produced by the reaction between alumina and carbon, and Al Ch gas reacted with Al404C and Al4C3 to produce Al Cl gas. Metallic aluminum was produced due to the disproportionation of A!Cl gas and condensed on the collecting plate. Meanwhile, the initial temperature of carbothermic reduction of alumina reduced in vacuum compared with that in normal pressure.IntroductionIndustrial production of primary aluminum is carried out in alumina cell by the so-called Hall- Heroult process, necessitating the use of very high currents of low voltage. The alumina from which metallic aluminum is gained must be chemically pure, otherwise impure metal results. The main drawbacks of the electrolytic production are its very high energy consumption, the release ofperfluorocarbons, and the high specific C02 emissions [1]. During the past years, there were a lot of attempts to produce metallic aluminum by carbothermic reduction of A1203 [2, 3]. Cox [4] determined the vapor pressure over the A1203-C system and performed X-ray diffraction analysis of condensed products. It was demonstrated that an increase in the carbon content in the system leaded to the sequence of transitions: A1203~Al404C~A1zoc~A14C3 ~AI [5]. In any carbothermic reduction process for aluminum, extremely high temperatures (2000 °C ) were required [6]. In spite of considerable effort, the carbothermic reduction of alumina to aluminum remains a formidable technical challenge, due to the high temperatures required, and to the formation of aluminum carbide and oxycarbide byproducts [7]."

Jan 1, 2013

By David R. Sadedin

The highly negative Gibbs free energies of hydrogen atom reactions suggest that refractory oxides such as titanium dioxide should be easily reduced by hydrogen atoms. These reactions appear to be most favourable at low temperatures; oxides should be reducible even at room temperature. Since hydrogen atoms are produced in plasmas containing hydrogen a number of investigators have used hydrogen plasmas of various sorts to test these possibilities for reducing refractory oxides, in particular TiO2. None of these attempts has succeeded, a small degree of reduction being achieved in only a thin layer near the surface. A deeper consideration shows that several factors complicate the reactions expected on the basis of the negative Gibbs free energy. One factor is that the back reaction by water molecules produces molecular hydrogen, not hydrogen atoms, and the metal atoms that have been reduced may be immediately re-oxidised. In plasmas there are complications due to diffusion, thermal and charge boundary layers and charged particle reactions. Interpreting the results of hydrogen atom reactions is difficult. Hydrogen is not detectable by electron dispersive spectroscopy and amorphous products are not determinable by x-ray diffraction. Another consideration is economics. The cost of producing hydrogen atoms has a large bearing on the metals for which hydrogen atom reduction may be competitive. In this paper these factors are discussed, some necessary basic studies are highlighted and the general principles of a laboratory reactor are given, together with the results of tests using ZnFe2O4, ZnO and TiO2 as test oxides.

Jan 1, 2006

By Andrew Shabalin, Vladimir Skorohodov, Svetlana Babaeva, ?lga Makovskaya

"At processing of some kinds of wastes (electronic scrap, secondary materials, spent nuclear fuel) in nitric acid solutions, and also in technology of silver refining, the significant amounts of palladium and platinum passes into a solution. The ion-exchange concentration of palladium and platinum in nitric acid solutions (5-500/dm3) are investigated. More than 30 various classes of ionites are tested. The most chemically resistance resins at the given conditions are identified. It is shown, that the maximum sorptive capacity to studied metals at high acidity the complexing, synthetic and inorganic sorbents possess. To definition of platinum metals sorption optimum conditions the kinetics is studied, isotherms of a sorption at various parameters from nitrate solutions are obtained. The conditions of the platinum and a palladium desorption from the pregnant sorbents and its regeneration with the subsequent reuse of materials were defined. The raw materials containing precious metals have very diverse composition and physical properties. Commonly the materials are processed by hydrometallurgical way. If gold or PGMs there are in raw materials to its opening hydrochloric acid solutions are applied. As an oxidizer nitric acid, hydrogen peroxide, gaseous chlorine, etc are used. Nevertheless, at processing of argentiferous materials and preliminary treatment of a waste including the spent nuclear fuel, nitric acid solutions are often used and the specified metals in some extent pass into solution [1]. Therefore selective extraction of PGMs from nitrate solutions is an actual problem. In the present work the ion-exchange concentrations of palladium and platinum in nitric acid solutions (5-500 g/dm3) are investigated. At the testing more than 30 various classes of ionites the most chemically resistance resins at the given conditions are identified. These resins are synthesized on the base of polyacrylate, styrene-divinylbenzene and vinylpyridine. For a selection of the most effective resin among what are made in Russia and overseas, a number of ionites with various functional groups were studied. Influence of functional groups type on a PGM sorption is shown for extraction of a palladium as an example (table 1). The presented data shows, that palladium concentration in a phase of ionites depends on sorbent type. If the increasing of solution acidity essentially reduces palladium sorption by sulfonic cation-exchange resins (KU-2×8) than its sorption by strongly basic anionites is approximately equal. Intermediate position is occupied by complexing sorbents. The latter (AN-31, SN-3, ANKB-35, Lewatit TP 207, Purolite S 930) are the most effective for extraction of PGMs from nitrate solutions from the point of view of capacity value. According to [2], solution behavior of Pt (II) and Pd (II) are similar. As is known from coordination chemistry, ligand environment of the metal ions substantially impacts to character of electronic spectra. The figure 1 shows the results of measurements of optical density of platinum bearing solutions with various concentration of nitric acid at ?=400 nanometers"

Jan 1, 2008

By Susumu Imashuku

A pseudoternary phase diagram of the BaO?ZrO2?ScO1.5 system is established and the conductivities of the scandium-doped barium zirconate are measured in wet conditions. According to the phase diagram, the molar fraction of scandia in the barium zirconate phase that equilibrates with the cubic zirconia (ZrO2) and scandia (Sc2O3) phase is 0.03. On the composition line, where the molar fraction of barium oxide (BaO) is 0.50, the solubility of scandia into barium zirconate is 0.27 as a molar fraction of scandia. At around 500 °C, the conductivities of scandium-doped barium zirconate are estimated to be almost same as that of yttrium-doped barium zirconateThe activation energies for bulk proton conduction in scandium-doped barium zirconate (0.57 eV for BaZr0.90Sc0.10O3-d) are higher than that of yttrium-doped barium zirconate (0.44 eV for BaZr0.90Y0.10O3-d). In addition, the bulk conductivity of scandium-doped barium zirconate in this study is 10 times higher than the reported conductivities in the temperature range of 75 °C to 300 °C.

Jan 1, 2006

By Pinakin C. Chaubal

Today?s steel industry is in a vibrant and resurgent mode. This transformation has been in the making for some time now. Over the last few decades, the industry was steadily transforming itself into becoming a high tech industry. New technology was adopted, efficiencies were enhanced, lean manufacturing concepts were brought in and a strong customer focus was developed. Today?s mills employ sophisticated instrumentation, computerized monitoring, on-line smart systems etc. driving processes that are producing at rates of many tons/minute. All this is not possible without judiciously using the latest available technologies in various fields and developing a more sophisticated work force. Prof. Sohn has been a pioneer in driving the concept of process engineering in process metallurgy. In this paper the focus is on some aspects of process engineering ? primarily process modeling - as applied to iron and steelmaking processes. Examples are shown to demonstrate how problems have been addressed. Some thoughts on future directions are presented.

Jan 1, 2006

By V. A. Bryukvin

It has been found that by superimposing symmetric alternating current over the process, the rate of nickel and cobalt leaching from metallized products with copper sulfate solutions increases by a factor of 1.5 to 2.0 and the apparent activation energy of the process investigated is reduced from 12 down to 6.6 kcal/mole. It appears especially attractive to use alternating current for anodic dissolution (oxidation) of metallic scrap of refractory metals and their alloys in ammonia electrolytes permits production of high-grade commercial products in the form of respective ammonium salts using a short and virtually reagent-free process flowsheet. Similar approaches can be applied also for electrochemical processing of nickel and copper scrap in sulfuric acid media with subsequent recovery of pure sulfate salts or electrolytic processing. Electrochemical technology for recycling of tungsten-cobalt (WC 15) and tungsten-rhenium (WR 20) alloys has been also investigated. In the former case, anodic oxidation of carbide alloy was carried out in nitric acid electrolyte with production of pure tungstic acid. The research conducted has indicated that the physicochemical effect of alternating current results in a lower activation energy of electrode reactions due to changes in the mechanisms of the electrode reactions themselves.

Jan 1, 2006