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By R. T. Jr. Faria, H. Vargas, R. Toledo, S. Cosin, V. P. Souza

"With the purpose of decrease environmental impact, caused by industrial residues (just discarded in the environment) and clay extraction in the ceramic industry, sanitary ware wastes were incorporated into clay. In contrast, it is important to evaluate not only the technological essays but also gases emissions in the ceramic firing process. The pollutant gases emitted in ceramic with residues can be in much larger concentrations than that in a pure clay ceramic firing or, on the other hand, can decrease the pollutant gas concentrations. With the aid of thermal analyses and photo acoustical techniques it was observed that sanitary ware waste can reduce the C02 emission. The gas emissions were shown as in function of firing temperature from 300 DC to 1100 DC. In order to analyze phase transformations during the firing process, clay samples and wastes were both analyzed by x-rays fluorescent chemical analysis and x-rays diffraction.IntroductionResearch works on the structural and physical changes that wastes, mainly industrially produced, cause to the final ceramic product has been rapidly expanding in these last two decades. See, for instance references in [1]. In spite of these examples of a continuous effort to incorporate wastes into clay ceramic motivated by technical and economical advantages, environmental issues are still a matter of concern. However, the gas emission due to the clay firing process and its related atmospheric pollution may be enhanced as a consequence of an incorporated waste [2]. It is known that the firing of clay ceramics in conventional furnaces using fuels such as wood, charcoal, heavy oil and natural gas generates appreciable amounts of gaseous components, mainly carbon dioxide (CO2), carbon monoxide (CO) and methane (CH4). Additionally to the atmospheric pollution, these gas sets could be harmful to the human health and can corrode equipments [3,4]."

Jan 1, 2012

By Ronald J. Roman

The shrinking core model for coarse particle leaching has been generally accepted as describing the leaching of a copper oxide or sulfide ore. However, when a mixed oxide/sulfide ore-is leached this model can not be used in its simple form because at least two and possibly three separate leaching processes are occurring simultaneously (dissolution of oxide copper minerals, secondary copper minerals and primarily copper minerals). It has been impossible to isolate their individual leaching curves from the recovery/time curve generated by the column leach test. This paper describes a tests program carried out at the Groupo Mexico, Mexicana de Cobre's La Caridad operation in which the individual recovery/time curves for the leaching of copper oxide mineral, secondary copper mineral and primary copper minerals were developed from standard column leach tests. Once the individual recovery/time curves were developed scale-up of the column leach test results to the commercial heap leaching operation is possible by using the shrinking core model.

Jan 1, 1999

By David Dreisinger

The pressure oxidation of pyrite is an important hydrometallurgical technology, especially in the total oxidation of refractory gold ores and concentrates (gold is locked in the pyrite structure preventing direct cyanide recovery). It has been noticed in some commercial applications and benchscale studies that the leaching of pyrite may be slow and apparently can be inhibited by the presence of molten elemental sulfur in the leach pulp. The purpose of this study was to determine whether Ortho-Phenylene-Diamine (OPD) could be used as a surfactant or dispersant for sulfur in the pressure oxidation of pyrite. OPD has previously been shown to be useful for pressure leaching of zinc and copper sulfides at 150 C.In this work, the interfacial chemistry of sulfur was studied at temperatures of up to 190 C in the presence and absence of OPD and other surfactants. The contact angle between molten sulfur and pyrite was also measured. Finally, the impact of OPD on the kinetics of pyrite oxidation was measured in bench-scale pressure oxidation experiments. The essential finding of this study was that OPD lowers the interfacial tension between molten sulfur and acid solutions and increases the contact angle (reduces wetting) between molten sulfur and pyrite. The work of adhesion between sulfur and pyrite was reduced by more than an order of magnitude in the presence of OPD. In bench scale tests, addition of OPD was found to significantly accelerate the rate of oxidation of pyrite. Conveniently, it was found that OPD was also fully degraded during high temperature oxidation processes. No residual OPD was detected in solution or solid samples from the leach testing. OPD is recommended as a sulfur dispersant in the pressure oxidation of pyrite and/or elemental sulfur containing feeds.

Jan 1, 2003

By Carl A. Kuehn

At Carlin, Nevada, non-indigenous hydrocarbons were introduced as a bitumen phase which was mobilized due to burial under the Roberts Mountains allochthon. similarly, some indigenous organic matter was locally mobilized. Fluid inclusion and paragenetic data of veinlets formed during this hydrocarbon stage, combined with quantitative modelling or organic maturation, indicate that host rocks had evolved past dry gas conditions of around 1550 and l.l+0.2 Kb in the presence of CH4-saturated, highly saline brine by no later than early to middle Cretaceous time. All hydrocarbons present would have been rendered immobile under these catagenic conditions. Crosscutting relationships at several scales suggest that hydrocarbon mobility may have ceased prior to the intrusion of a series of dikes in the mine which have subsequently been altered and mineralized. Apart from subsequent oxidation, the current distribution and high maturity of carbon-rich zones were established prior to gold introduction. No Evidence has been found supporting proposed hydrocarbon "remobilization" during or after gold mineralization and alteration. The high density of the CH4-bearing fluid requires formation at high pressures (near 1 Kb) and precludes their formation as a result of the "cracking-off" of CH4 from organic matter during a thermal event associated with a shallow hydrothermal system. The density and composition of the fluid inclusions restricted to the early hydrocarbon-stages of the Carlin paragenesis are not unique to the sediment-hosted gold deposit environment of north-central Nevada. Similar inclusions are found in authigenic quartz crystals from Paleozoic carbonaceous shales in central Pennsylvania which have experienced normal metagenesis of indigenous organic matter due to deep burial.

Jan 1, 1987

By Pieter Steeneklm, Mazi’ Rejaee

"EXECUTIVE SUMMARYThe automotive industry's search for increased fuel efficiency through component weight reduction has driven the growth in consumption of magnesium metal in the form of die cast alloys. This trend, which began in North America and should soon accelerate in Europe, will require enhanced recycling services since each tonne of metal used for die cast parts production produces about 500 kg of scrap.Currently, the European die cast market is plagued by very high tolling prices for scrap recycling due to lack of competition and high transport costs due to the distances between the scrap generator and the recycling facility. This situation clearly increases the cost of magnesium die cast components and reduces magnesium's competitiveness with other materials. The challenge for the magnesium industry in the short term is to provide cost ·effective recycling solutions for the die cast industry. In addition effective recycling, in the medium to long term, is needed for the anticipated large volumes of secondary or used scrap that will become available as the die cast components reach the end of their life cycle. This paper will present The Antheus Integrated Magnesium Project as a Novel approach addressing some of the key recycling related issues facing the magnesium industry, in particular the die casters. The paper outlines the many advantages of an integrated magnesium metal park, in an overall goal of increasing magnesium metal's competitiveness."

Jan 1, 2000

By Takeshi Yoshikawa

For the sake of effective control of titanium-compound inclusions in the steel-making processes, especially for stainless steel production, the influences of alloying elements of chromium, nickel, manganese, molybdenum, copper and oxygen on the thermodynamic property of titanium in molten iron were investigated at 1873K. At a certain titanium potential controlled by the coexistence of Ti3O5 and Ti2O3 doubly saturation of steels, the interaction parameters between alloying elements and titanium in molten iron were determined as follows. [ ] From the investigations on the equilibrium of titanium deoxidation in molten iron, the activity coefficient of titanium and the first order interaction parameter between oxygen and titanium were determined as follows. [ ] Also, deoxidation equilibrium for titanium in molten 304 stainless steel was measured and compared with the calculated results using the determined interaction parameters.

Jan 1, 2006

By Nan Zhang, Lei Zhang, Gai-feng Xue, Lina Wang, Pu Liu

"A novel ß-diketone modified silica gel was synthesized by a simple reaction. The prepared material was characterized by diffuse reflectance FTIR spectroscopy and it was used for the adsorption of heave metal ions in the industrial waste water. The main parameters affecting the sorption of heavy metal ions, including pH, water flow rate, and elution, have been investigated in detail. Under the optimized operating conditions, most of the targeted heavy metal ions could be removed. The material could be simply regenerated by hydrochloric acid solution. The method is rapid, selective, economic and applicable to the removal of heavy metal ions from industrial waste water.IntroductionToxic organic pollutants and heavy metals ions mainly from industrial activities such as plating, metallurgy and dyeing industries, are a threat to human health and the surrounding environment, because of their toxicity and persistence after being released into the natural environment [1]. These pollutants must be removed or degraded to an acceptable level, before being discharged to the receiving waters. Therefore, detection and determination of heavy metal ions in industrial waste water is very important.Inductively coupled plasma optical emission spectrometry (ICP-OES) is the most used technique for the determination of heavy metal ions because of its capability for rapid multi-element detection over a wide concentration range and with relatively low detection limits. Compared to other techniques such as neutron activation analysis (NAA), X-ray fluorescence spectrometry (XRF) and inductively coupled plasma mass spectrometry (ICP-MS), ICP-OES has the above advantages. Some constituents in industrial waters, such as organic compounds and inorganic salts, may cause matrix effects. In order to achieve accurate and reliable results, an efficient preconcentration of heavy metal ions and their separation from the matrix are usually required."

Jan 1, 2012

By KNona C. Liddell

The time and spatial dependence of component and species concentrations during in situ uraninite leaching have been modeled using a reactive transport model based on partial equilibrium between reactive minerals and the solution. The flow field is represented by mixing cells in series. The effects of the H2O2, (NH4)2CO3, and NH4HCO3 component concentrations have been simulated, and results are presented for a one-dimensional flow field.

Jan 1, 1995

By Zhang Libo, Wang Xin, Peng Jin-hui, Ju Shaohua, Guo Sheng-hui, Xu Lei, Huang Meng-yang

"China is lacking high grade titanium ores. This work intends to leach impurities such as Fe, Ca and Mg from a low grade titanium ore, to increase the grade. The original material contained 65% TiO2 , 16.12% Fe, 9.4% CaO + MgO, 4.2% SiO2, 1.25% A12O3, and the particle size is between 0.053-0.045mm. Microwave energy was used to enhance the leaching effect. The results showed that when normal heating was used to leach the mineral, the extraction of impurities Fe, Ca and Mg was very low. However, when microwave energy is introduced, the extraction of Fe, Ca and Mg increased dramatically. The optimized conditions are: relative power 5W/g, the ratio of concentrate to HC1 isl5%, leaching at 160°C for 20 min with a ratio of liquid to solid 12:1 mL/g. The material obtained under these conditions contains 92.73% TiO2, 0.207% Ca + Mg, 0.8% Fe, with 94.6% Ti recovery. The poduct meets with the quality for boiling chlorine.IntroductionThe resources of titanium are very abundant, and are distributed all over the world. There are almost 140 minerals containing TiO2 with a content of more than 1%. However, there are only several minerals which can be used for producing sponge titanium. They are mainly rutile and ilmenite. The grade of nature rutile concentrates is higher than 95% TiO2, and it is a high quality raw material. But the resources of nature rutile are relatively low; after mining for many years, its resources are exhausting gradually. Although ilmenite reserves are great, ilmenite cannot be used as a raw material because of its low content of TiO2, only 45-70%; also it has a high impurity content of Ca, Mg and Fe. In these years, there is a tendency for titanium industry to use high grade concentrate."

Jan 1, 2012

By R. Escalera-Lozano, M. Herrera-Trejo, M. A. Pech-Canul, J. López-Cuevas, A. L. Leal-Cruz, M. I. Pech-Canul

"The use fly-ash (FA) and rice-hull-ash (RHA) offers the potential for the manufacture of hybrid Al/SiCp/spinel composites via reactive infiltration, both with recycled aluminum. The main reason behind this statement is the beneficial role that both waste materials play in preventing the degradation of SiCp reinforcements when the composites are processed with aluminum in molten state. Experimentally, MgAl2O4 is formed in situ during the infiltration of SiCp-preforms in the temperature range 1050-1150 oC for 50-70 min in argon atmosphere at a pressure slightly above to that of the atmospheric pressure. Results reveal that both FA and RHA help in preventing SiCp dissolution and the subsequent formation of the unwanted Al4C3; and although FA-composites still might be susceptible to corrosion via Al4C3 -by the interaction of native carbon in FA with liquid aluminum- a proper FA treatment significantly mitigates its deleterious effect. Primary corrosion mechanisms and strategies to overcome the potential degradation effects are outlined.IntroductionOwing to inherent materials characteristics and post-processing complications –such as corrosion damage- development of metal matrix composites (MMCs) from recycling/waste sources might be a challenging task. Fly-ash (FA) and rice-hull-ash (RHA) are two primary waste materials that offer excellent opportunities for the development of Al matrix composites. Due to its singular hollow-spherical shape and low density, FA has attracted the attention of many researchers. For this reason, most of the efforts to develop Al-based composites from waste materials have been centered on the use of fly ash. Extensive research efforts in the use of FA for Al-based composites have been undertaken by Rohatgi and coworkers [1-4]. In addition to lowering costs, incorporation of fly ash into aluminum has been proved to decrease the materials’ density, increase their hardness, abrasion resistance and stiffness [1]. One of the major outcomes from the mechanical evaluation of aluminum composites prepared with fly ash is that related to their compression characteristics. Typical compressive stress-strain curves form A356/hollow fly ash composites show a linear elastic region followed by a plateau (associated to the collapse of the hollow particles), and then an increase in stress, representing densification of the foam. The crushing of the cenospheres in the composites has been related to an enhancement in the energy absorption capabilities of the material and to a better damage tolerance [4]."

Jan 1, 2008

By Huang Chao

The thermodynamics analysis on reducing-matting smelting of sulfide ore of lead, antimony and bismuth which use ferric oxide as sulfur fixed agent is first analyzed. Due to the analysis of reaction mechanism, ferric oxide is first reduced to ferrous oxide, then ferrous oxide produce reducing-matting reaction with sulfide ore and reducing agent as reaction equation: MeS+FeO+CO=Me+FeS+CO2. The reaction thermodynamic calculation shows that the reducing-matting reactions of lead sulfide, antimony sulfide, Jamesonite, and bismuth sulfide are feasible, but is infeasible for zinc sulfide. These conclusion provide a feasible method for solve the pollution which produced in the smelting of sulfide ore of lead, antimony and bismuth.

Jan 1, 2006

By Junji Shibata

As one of the effective usages of various wastes discharged in non-ferrous metal industry, the synthesis of hydrotalcite was carried out using aluminum dross as a raw material. Hydrotalcite is one of the inorganic anion exchangers and has layered structure of complex hydroxide. The removal of toxic metal ions such as As(III), As(V), Cr(VI) and Se(IV) with the hydrotalcite was investigated, and the removal properties were compared from the viewpoint of the anion exchange amount and exchange rate. Hydrotalcite can be obtained by a co-precipitation method from the aluminum dross and the waste MgCl2 solution discharged in an aluminum regeneration process. Slight amounts of SiO2, Al2O3, Fe2O3 and so on remain in the reaction product as an impurity component. Interlayer distance of the obtained hydrotalcite is about 0.3nm. Hydrotalcite changes to Mg-Al oxide by the calcination at 773K for 3h, and then hydrotalcite is formed again by a rehydration operation after calcination. The toxic metal ions are removed from aqueous solution by the anion exchange reaction in the pH region where toxic metal ions exist as the anionic species like AsO2-, HAsO42-,CrO42-, and SeO32-. The exchange amount is considerably concerned with the valence of anionic species and the size of anionic species. The removal of toxic metal ions were investigated from the engineering aspects such as the low concentration limit to be removed, the amount of hydrotalcite to be used for the perfect removal of toxic metal ions and so on.

Jan 1, 2006

By Admire Chaendera

A gas jet was blown through submerged nozzles to stir the bath in the presence and absence of slag. Mixing and mass transfer rates were then studied. Water and kerosene (10% by volume) were used to simulate the metal and slag phases respectively in the cold model. The mixing time (Tmix), defined at 99.66% bath homogeneity level, increased with bath height and decreased with an increase in the gas injection rate. Its value in the model vessel was related to gas flow rate (Q), bath weight (W), and bath height (H) by, Tmix = 4.39Q-0.73W0.24H1.12. Inclusion of the slag phase increased Tmix by about 16% and the mass transfer parameter, [(Reloc,r)0.25(Ret)0.32], values by about 32%. Mass transfer rates were higher near the bath surface and in the gas-liquid plume region. They increased with gas flow rate but decreased with an increase in bath height. The relationship, K Q0.08, showing derived mass transfer coefficient (K) dependence on the gas injection rate (Q) was established. The proportionality constant in the equation varied with gas flow rate and sample location.

Jan 1, 2006

By M. J. Perpich

Electrochemical and chemical leaching tests were carried out on chalcocite, covellite and chalcopyrite in acidified iron sulfate solutions sparged with a mixture of O2 - SO2. The gas mixture catalyzed the ferrous to ferric oxidation reaction in situ and, therefore, increased the redox potential and oxidizing strength of the solution. Anodic polarization curves in dilute sulfuric acid on copper sulfide electrodes showed that chalcopyrite passivates and dissolves at current densities orders of magnitude less than chalcocite and covellite. The addition of a depassivating agent (Ag+) increased the passive current density of chalcopyrite and caused breakdown near 0.625 V (SCE). The depassivating effect was also observed during the leaching of chalcopyrite particulate samples as small amounts of Ag+ added to acidified iron sulfate solutions in the presence of O2 - SO2 mixtures greatly increased the leaching rate and the total amount of Cu oxidized (> 90%). Passivation was prevented in the absence of Ag+ by decreasing the initial oxidizing power of the solution and by pretreating the sample in a reductive leach. Both of these methods resulted in transformation of the chalcopyrite surface from its characteristic greenish-gold into deep black. Increased concentrations of Fe+++ due to 02 - S02 sparging were then able to oxidize the transformation product.

Jan 1, 1999

By Jonkion M. Font

As a comprehensive contribution to the understanding of oxygen-blowing of matte smelting, the copper and nickel solubilities between the FeOx SiO2-MgO slag with saturated SiO2 and the Cu2S-Ni3S2 FeS matte with the NCu/(NcU+NNi) of 1, 0.75, 0.5, 0.25 and 0, in a MgO crucible were investigated at 1573 K under controlled partial pressures of SO2 at 0.1, 0.5 and 1 atm. The partial pressures of SO2, S2 and O2 were controlled by using an Ar-SO2-S2 gas mixture after passing through a sulfur reservoir. It was clarified that, at a given matte grade, the solubility of copper in the slag was independent of pso2 while that of nickel increased with increasing pso2. This notable difference was considered to be ascribable to the chemical formulas of the mono-metallic sulfides in which one copper atom combines with ½ sulfur atom while one nickel atom combines with 2/3 sulfur atom. It was also clarified that, at a given iron content in the matte, the pot and ps2 were independent of the matte species. This was ascribable to aFeS in the matte, which was independent of the matte composition, Ncu/(Ncu+NNi), at a given iron content in the matte.

Jan 1, 1999

By Okechukwu Anopuo, Gerhard Tober, Petra Maier

"In this study, an investigation on the microstructure of hot rolled steel S355J2+N was conducted to optimize process parameters of complex forming, which combines rolling and bending. The best sets of parameters are worked out based on homogeneous mechanical properties and microstructure within the varied deformation degree with maximum at <p = 1.14 on a 25 mm thick plates. Mechanical properties, especially of heavy plates, are strongly influenced by the local deformation degree, strain rate and temperature. Detailed microstructural analyses showed that the ferrite-pearlite band structure changes near the surface, while maintaining homogeneous microstructure within the deformed work piece. Surface decarburization was also observed and this leads to decrease in hardness. To minimize iron oxide formation which could lead to side cracking, reduction in exposure time to temperature was suggested. On the other hand, temperature reduction below a critical value would risk the accurate forming process.IntroductionThis work presents the preliminary results of research to develop a new complex deformation process of thick steel plates. Complexity is given because the forming process combines rolling to reduce thickness and profiling by bending. The work piece will experience a thickness reduction from 25mm to 8 mm and is double curved. To explain and understand forming of thick plates basics of sheet forming as well as massive forming need to be used. At the moment there is no forming process established to produce double curved plates including reducing thickness in one process step. Technologies nowadays consist of two process steps: flat rolling and pressing in shape. Due to good weldability and formability the final product will be made of steel S355J2+N. This low-carbon steel is well understood and has a low strengthening exponent, which is expected to keep the forming forces down. Reduction of thickness from 25 mm to 8 mm gives furthermore a high deformation degree. Thus, hot forming has to be applied. The determination of process parameters is the main aim of overall research project; temperatures above lOOO°C are expected. Flow curves in literature are given at various temperatures and strain rates [1]. However, experiments with data close to the industrial application are rarely found, especially at low strain rates and high deformation degrees. Pre-test were done by flat rolling, being aware that the influence of bending is eliminated. The microstructure evolution were characterised in relationship to material formability with special attention to grain size change and recrystallization. Representative samples should be selected from specific locations in the deformation zone according to the knowledge about the metal forming process [2]. Due to no further alloying elements in S355, no precipitation hardening is expected to take place during hot forming, which keeps the mechanisms simple and the concentration on the feasibility of the complex forming process is given."

Jan 1, 2012

By Riyad N. Ahmad-Bita, Shadia J. Ikhmayies

"SnO2:F/CdS:In structures were prepared by the spray pyrolysis technique on glass substrates at a substrate temperature Ts = 450°C. NH4F and HF were both tried as the sources of fluorine in the precursor solution of SnO2:F. A comparison between the properties of structures obtained by using the two doping compounds was performed. X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmittance measurements were used to characterize the films. The structures prepared by using HF as a fluorine source were found to have more ordered crystal growth, larger grain size and sharper absorption edge. From the inspection of the first derivative of the absorbance it is expected that more interdiffusion on the SnO2:F/CdS:In interface takes place in the structures made by using HF. These results confirm that these films are better as forecontacts for CdS/CdTe solar cells.IntroductionThin film CdS/CdTe solar cells built in the superstrate geometry rely on transparent conducting oxides (TCOs) to make the front contact The investigation of combined CdS-TCO films has recently been developed owing to the great interest of better understanding the effect of these bilayers on the absorbers [1]. Usually SnO2 is utilized as a front contact for these solar cells. Optimizing the properties of the SnO2/CdS structures is an important step on the way to get high performance CdS/CdTe solar cells.There are different methods to prepare SnOz thin films, such as reactive sputtering [2], evaporation [3], chemical vapour deposition [3, 4], dip coating [5] and spray pyrolysis [6-9]. At the same time CdS thin films can be prepared by different techniques such as chemical bath deposition [10], thermal evaporation [11], screen printing [12] and spray pyrolysis [7, 13]. However, the spray pyrolysis technique is a very low cost and simple technique that enables intentional doping and getting large area and uniform thin films [14]. For these reasons it is choused to prepare SnOz and CdS thin films in this work. To improve the properties of these compound semiconductors, SnOz was doped with fluorine and CdS was doped with indium where such doping is well known for these compounds."

Jan 1, 2012

By V. Bhagavathy

This paper describes a method for the determination of traces of rare earths using energy dispersive x-ray fluorescence spectrometry (EDXRF) after preconcentration of their oxine complexes onto activated carbon. Various parameters that influence adsorptive preconcentration of rare earths onto activated carbon viz. pH, amounts of activated carbon and oxine, time of stirring and aqueous phase volume were systematically studied. A numerical method based on simple least square procedure using fifth order polynomial with 25 consecutive values was developed for smoothing and differentiation of EDXRF data which was previously digitized and averaged. First order derivative EDXRF in conjunction with adsorptive preconcentration on activated carbon enables to determine as low as 10 ppb of each of individual rare earth elements.

Jan 1, 1989

By J. Rajesh Kumar

The extraction equilibrium study of tetravalent platinum was carried out using tri-octyl/decyl amine (Alamine 336) and bis(2,4,4-trimethylpentyl) monothiophosphinic acid (Cyanex 302) in kerosene from hydrochloric acid media to investigate their extraction capacity, since they have different donor atoms, ?N? and ?S?. Their distribution equlibria were studied as a function of acid, extractant, diluents and temperature. The title metal shows the inverse behavior at higher acid concentrations. Extraction of tetravalent platinum increases with increase of extractant concentration. The plot of log D vs. log [Extractant], mol.L-1 is linear with slopes 1±0.3, indicating the association of one mole of extractant with the extracted metal species. Stripping of metal from the loaded organic (LO) with mineral acids and bases such as hydrochloric, sulphuric, nitric acids and ammonia, hydrogen peroxide, sodium hydroxide, thio- urea were studied. Regeneration and recycling capacity of Alamine 336/Cyanex 302 and extraction behavior of associated elements was also studied.

Jan 1, 2009

By Yves Fautrelle, Kader Zaidat, Hervé Combeau, Miha Zaloznik, Mohammed M'Hamdi, Bachir Saadi, Xiaodong Wang, Knut Omdal Tveito

"Numerical simulations of macrosegregation formation during horizontal solidification of a hypoeutectic Sn-Pb alloy in a rectangular cavity is presented and compared to experimental results. The experiment involves a melting phase, a holding stage at constant temperature with/without application of electromagnetic stirring, and finally solidification. We simulate all stages of the experiment and study the segregation of Pb throughout the experiment. A twophase volume averaged model is used for the numerical simulations, accounting for thermosolutal convection and assuming perfect microscopic mixing (lever rule). The influence of the melting phase and the electromagnetic stirring is studied with different cases to illustrate the consequences on the flow pattern and Pb segregation. The numerical simulations are compared to the experimental data and the impact of chemical inhomogeneities prior to solidification on macrosegregation formation is discussed.IntroductionMany extensive investigations have been performed so far on the solidification of metallic alloys. However, the melting process of metallic alloy has not attracted attention in a same manner. Nevertheless, melting of alloy may put forth peculiar effects as described in the present paper. It has been observed from a benchmark experiment [1, 2] that significant stratification might arise during the melting process of Sn-Pb alloy. That effect was put forth thanks to the analysis of the experimental temperature distribution which indicated that the convective fluid flow was almost zero. The effect was enhanced when the lead composition was higher (above 6wt.%). The present paper is aimed at confirming that the melting of an alloy containing a heavier solute may be accompanied with a stratification of the solute which exerts a stabilizing effect on the convective fluid flow. Results obtained from numerical modeling are compared with experimental data obtained from the benchmark facility."

Jan 1, 2012