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By Dai Xi

In the present work, the viscosities of molten FenO-MgO-SiO2 and FenO-MgO-CaO-SiO2 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 II 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-SiO2 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 Fe3O4 on the viscosity was quite significant. The viscosity of slag increased by 300mPa-s at 1573K when Fe3O4 content varied from 3 to 9 mass%. The viscosity values are presented as the functions of temperature and composition. A comparison between FenO-MgO-SiO2 and FenO-MgO-CaO-SiO2 systems is given in this study.

Jan 1, 2003

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 P. A. Davidson

"We discuss the influence of a static magnetic field on jets, vortices and turbulence. This is particularly relevant to D.C. braking in slab casting. Our main conclusion is that, typically, the magnetic field destroys mechanical energy, via joule dissipation, but is unable to destroy momentum. Rather, it continually rearranges the momentum in such a way that the energy falls.IntroductionIt is well-known that a static magnetic field can suppress motion of a liquid metal. That is to say, movement of the liquid across the magnetic field lines induces a current. This leads to Joule dissipation and the resultant rise in thermal energy is accompanied by a corresponding fall in kinetic energy.This phenomenon has been exploited in a range of metallurgical processes. For example, in the continuous casting of large steel slabs, an intense, static magnetic field is commonly used to suppress motion within the mould. The objective is to keep the free surface of the liquid quiescent, thus avoiding the entrainment of surface debris. In other solidification processes, such as techniques for growing semi-conductor crystals, it is widely believed that natural convection has a detrimental effect on the metallurgical structure of the solid. Again, the imposition of a static magnetic field is seen as one means of suppressing these unwanted motions. Finally, magnetic damping is used in the laboratory measurements of chemical and thermal diffusivities, particularly where solutal or thermal buoyancy can disrupt the measurement technique.In this paper we shall look at the damping of jets, vortices and turbulence. Our aim is to present a unified theoretical framework from which the many published studies may be viewed."

Jan 1, 1999

By Kan Song, Lin Liu, Hengzhi Fu, Jun Zhang, Haijun Su, Xiaojiao Jia

"Al2O3/YAG/ZrO2 eutectic in situ composite has been regarded as new generation of high temperature structural material due to its excellent performance even close to its melting point. The directionally solidified Al2O3/YAG/ZrO2 eutectic ceramics are prepared by recently developed Laser Floating Zone Melting (LFZM) apparatus in which a splitter mirror is used to obtain two beams with the same quality from one CO2 laser. With the two laser beams irradiate the sample from opposite directions, the sample is zone melted. The apparatus configuration and the solidification processing are described in detail. The solid/liquid interface morphology is studied and the mechanism of microstructure formation especially the characteristic of eutectic cellular is discussed. It is shown that YAG and ZrO2 phases play a leading role during the ternary eutectic growth. Meanwhile, the relationship between the solidification microstructure and the processing parameters are investigated.IntroductionAl2O3/YAG/ZrO2 ternary eutectic in situ composite, due to its excellent high temperature mechanical properties, is now considered to be a promising candidate material as a replacement of nickel based super alloy for new generation aero space engine turbine blade [1]. They exhibit flexural strength of 360-500 MPa from room temperature to 2073K in air atmosphere [2]. The compression creep strength at 1873K is 433MPa with the strain rate of 104/s [3]. However, because of the high melting point and complex physical properties, there remain still many difficulties for its application. One of the bottlenecks is the poor understanding of the relationship between microstructure and solidification conditions."

Jan 1, 2012

By Jorge A. S. Tenorio, Girley F. Rodrigues, Joner O. Alves, Denise C. R. Espinosa

"Rock wools are mineral fibers composed of amorphous silicates, due to their thermo-acoustic characteristics this material has a broad consumer market in the construction, automotive, and electric-electronics industries. This work studied the recovery of wastes from ornamental rocks (granite and marble) as partial raw materials in the production of rock wools. Residues from granite and marble cuttings are industrial wastes with considerable production and limited applications. These wastes should be appropriately managed because when discharged in rivers or lakes can cause siltation, and also they can cause serious human health problems, such as silicosis. Samples of produced materials with thickness smaller than 500µm were characterized by chemical analyses, XRD, and DTA. Results showed that the rock wools produced using granite or marble wastes have important properties, especially the melting point. This process decreases the extraction of mineral resources and provides a profitable destination for the ornamental rock wastes.IntroductionThe ornamental rocks industry is a sector with large production of wastes. During the granite and marble extraction processes and specifically during the rocks cutting (see Figure 1), approximately 35 tons of powdered rock per month can be produced. These residues should be appropriately managed, because when discharged in rivers, lakes or watersheds, they can cause siltation. Also, these wastes can cause serious human health problems, such as silicosis [1].Currently, the granite and marble wastes are mainly used in civil construction to produce materials in the form of mortar, bricks and tiles. However, due the current produced volumes and the average growth of world production estimated at 6% per year, new applications for these wastes are necessary [2]."

Jan 1, 2011

By L. Klinger, T. Werber, LA Levin, A Katsman

"The process of catastrophic carburization known as ""metal dusting"", whereby a solid metallic material is converted into fine particles in a carburizing atmosphere, was analyzed. It was shown that this conversion is the result of plastic deformation and subsequent fracture accompanying diffusional phase formation in the near-surface layer. The process is controlled by internal stresses arising during phase transformation. Competition between stress generation and relaxation may result in the attaining the ultimate strength in the near-surface layer and its fracture. Such a mechanism of metal disintegration may occur in a certain temperature interval depending on the kinetic and geometrical parameters of the system - the diffusivities of the alloy's components, the ratio between specific volumes of the new and the old phases, and the ultimate plastic strain. The temperature interval for disintegration of carbon steel, the rate of disintegration, and the period of the disintegration cycle, were evaluated and compared with experimental data. IntroductionCatastrophic carburization, known as ""metal dusting"", consists in conversion of a solid metallic material into fine particles. The process occurs in a carburizing atmosphere at elevated temperatures. The corrosion product, usually named ""coke"", consists of metallic particles dispersed in a loose carbon matrix. Under industrial conditions metal dusting takes place, for example, in a gas mixture of CO and H2 or in hydrocarbon environments. Steels, nickel- and cobalt alloys are susceptible to this kind of wastage in the temperature range 400-800°.A mechanism of metal dusting in steels was proposed by Hochman [1] and later developed by Grabke and coworkers [2-5]. According to the proposed model, the process consists of the following reaction steps:"

Jan 1, 1996

By Lichao Ding, Chunhua Liu, Yunnen Chen

"In this paper the simulated acid magenta dye discoloring the reaction process was researched. The results showed that it attained highest decolorization efficiency for acidic magenta simulation dye wastewater when pH 9 and reaction time 10 min. With the initial dye wastewater concentration increased, the decolored rate decreased. The decolored rate in general kept a tendency to increase with the temperature increased. Kinetics researches showed that when pH 9, reaction temperature 20 and 35 ?, the decoloring reaction process for the dyes accorded with the First-order dynamic equation. The decoloring reaction rate constant was influenced by initial concentration of dye wastewater and temperature.1. IntroductionIn China, textile printing and dyeing industry is one of industrial departments which using more water and discharging more wastewater. There is about 7 billion tons of waste water discharge each year, of which 80% from the process of printing and dyeing. Being complex ingredients, high chroma, more toxic substances and severe environment pollution, the treatment of printing and dyeing wastewater becomes problem urgent to be resolved. The traditional treatment methods such as adsorption [1], coagulation [2], biochemical method [3,4], which has advantages of simple equipment, simple operation and mature process, but they can cause waste accumulation and secondary pollution [5,6].Magenta is a kind of organic compounds, which classified into acid and alkaline magenta. Considering the advantages of simple operation, low cost, simple experiment equipment and friendly to environment, acid magenta dyes wastewater was chose as object in this paper. Some parameters such as pH, contact time, temperature and the initial concentration on of simulative acid magenta dyes wastewater were studied."

Jan 1, 2012

By Yanxia Lu

Porous silicon carbide (SiC) has been the top selection for diesel particular filters (DPFs) since 2000 because of its high thermal diffusivity and strong body, which help it to survive in the harsh environment of a diesel exhaust system. However, the process to produce SiC DPFs is a costly one. The work presented herein describes more cost effective composite materials for this application, namely Si-SiC and Si₃N₄-SiC. Both composites have shown excellent filtration efficiency, low back pressure and outstanding survivability of regeneration at high soot loadings. Since the composites are batched from silicon metal, they can be prepared by a low temperature process that is impossible in the production of pure SiC PDFs. In fact, fabrication of SiC composites simply involves reactions between nitrogen gas and silicon metal, or silicon metal bonded with SiC, and as such uses a much less costly process when compared to the one employed to make SiC. In addition, the pore structure of the composites can easily be tuned by selecting raw materials and changing the ratio of two components. A typical pore structure consists of well connected pores with a median pore size of 5-20 µm and a porosity of 40-55%. This talk will describe the exothermic behavior as well as the mechanical and thermal properties of SiC composites in comparison to those of SiC filters. It will also show the superior thermal shock resistance of Si₃N₄ bonded SiC which is due to the unique combination of these phases that lowers the thermal expansion and elastic modulus relative to pure SiC.

Jan 1, 2006

By Leah Penner, Thomas J. Ruth, Paul Schaffer, François Benard, Edouard Asselin, Stefan K. Zeisler, Thomas J. Morley

"This paper details the electrodeposition of metallic molybdenum from an aqueous, acetateelectrolyte containing molybdate ions. The deposition is carried out in a highly concentrated (up to I 0 M) acetate bath in the presence of a very low concentration of bone glue (60 µg/L). The molybdenum metal deposits are up to 20 µm thick and adherent. The deposits were characterized by XRD and XPS analysis. The deposition process is very inefficient, as up to 99% of the current is used to generate hydrogen during electrolysis. The effect of acetate concentration, pH, additives and current on the deposition efficiency and physical properties of the molybdenum deposit were investigated and optimized to obtain smooth, adherent coatings.IntroductionMolybdenum has increased thermal and wear resistance properties that are often utilized in material coatings [I]. These coatings are most often manufactured by sintering, pressing or spraying molybdenum powder at elevated temperatures, as a substitute method for standard metallurgical practices, such as electroplating [2, 3]. The lack of reports describing molybdenum deposition is most likely due to the highly oxophilic nature of molybdenum and the stability of its oxides, especially in water. Previous attempts to electrochemically reduce molybdenum from molybdate (Mool·) ions to molybdenum metal have reported the production of either a poorly adherent mixed oxide [4-6], or a thin(< 0.1 µm) metallic film [7-9]. Thick metallic molybdenum is capable of being co-deposited with one of the iron-group metals (Ni [10], Co [11] and Fe [12]) to produce an alloy [13, 14]. These alloys, however, may not be suitable for applications requiring pure molybdenum as they usually contain less than 50% molybdenum (often less than 30%)."

Jan 1, 2012

By Mark C. Bronson

The feasibility of several pyrochemical approaches-for separating non-radioactive constituents from ICPP HLW calcine were examined. The removal of aluminum as AICI3 from aluminia calcine was successfully demonstrated. The examination of pyrochemical processes to remove non-radioactive constituents, primarily aluminium, zirconium, calcium and fluorine, from zirconia calcine showed that fluorine removal was required in order to chlorinate the calcine. A molten calcium chloride wash, a calcium reduction, and. a sulfuric acid treatment were examined as possible zirconia calcine pretreatment options for fluorine removal. Fluorine removal from simulated ICPP zirconia calcine was demonstrated by both a CaCl2 wash method and a sulfuric acid treatment method. X-ray fluorescence analysis indicated that greater than 97% of the fluorine can be removed by either method. Fluorine removal by a calcium reduction using an alloying agent, zinc, or a calcium reduction using, a filtration separation were also demonstrated, but the efficiencies of fluorine removal were considerably less ranging from 50 to 90%. Regeneration of CaCl2 from the salt and oxide residues of the CaCl2 wash experiments was also demonstrated &apos;by an aqueous dissolution method. From the salt residue, 85% or more of the CaCl2 was recovered and contained little if any CaF2 or CaO. From the oxide residue close to 100% of the CaC12 was recovered. Because of the overall success of the CaCI2 wash, it was determined to be the preferred fluorine removal process. The sulfuric acid treatment to remove fluorine is effective, but the proposed overall flowsheet has not&apos; been adequately demonstrated.

Jan 1, 1995

By Beatriz Amarai Campos, Jorge Alberto Soares Tenorio1, Denise Crocce Romano Espinosa, Adriana Johanny Murcia Santanilla

"The aim of the present work is to investigate the recovery of nickel from obsolete cell phones printed circuit boards. The printed circuit boards were firstly submitted to a grinding process and then leached in sulfuric acid. Nickel was extracted from aqueous solution using Cyanex 272. Aqueous/organic ratio was 1/1. The effect of both pH and modifier addition on selectivity of extraction was investigated.IntroductionCurrently, electric and electronic equipments (EEE) have become a necessity to the modern life. Associated with this necessity comes the continuous and increasing replacement of those equipments by new ones. The accelerated technology advances are responsible for the generation of electric and electronic waste. This waste can be dangerous not only to human health but also to the environment. Waste of electric and electronic equipments (WEEE) has a variety of components and metals in its composition becoming a potential pollutant to the environment when not properly discarded. Its wrong disposal causes a loss of materials that could be recovered and reused. Therefore WEEE treatment is an important matter because it can assist the reduction of waste generated and the recovery of valuable metals.Printed circuit board (PCBs) is an essential component of EEE and is typically very complex from a chemical point of view. Several metals may be present in its composition, such as cooper, nickel, iron, zinc, lead, tin and silver1''. This characteristic hinders the development of a simple treatment, making it necessary the application of chemical and mechanical processing for their recycling'4'. The UN estimates that approximately 20 to 50 million of tonnes of WEEE are generated worldwide each year."

Jan 1, 2011

By Zbigniew Smieszek, Ryszard Chamer, Ryszard Prajsnar, Zygmunt Kurek

"Lead-containing wastes processed at the IMN’s Division in Legnica originate mainly from dry and wet dedusting installations of the technological lines for copper production. These are lead dusts and lead-zinc dusts characterised by the specific properties resulting from the chemical composition of the Polish copper concentrates. Besides lead, they contain many accompanying metals and impurities such as zinc, copper, sulfur, chlorine, potassium, sodium, and also bituminous substances. Processing of lead-containing dusts is conducted in the installations of rotary-rocking furnaces heated with gas-oxygen burners fitted with auxiliary systems for cleaning process gases and refining re-circulating dusts. The processing technology utilizes innovative process and technical solutions enabling disposal of lead-containing wastes from copper metallurgy and from non-ferrous metals industry according to the BAT recommendations and to the guidelines specified in integrated permission. In this paper, the main technological aspects of processing lead-containing dusts at the IMN’s Division in Legnica have been presented.IntroductionCrude lead is obtained in Polish lead metallurgy from various primary and secondary materials, such as Zn-Pb concentrates, lead-bearing dusts of copper metallurgy and battery scrap. In zinc smelter Miasteczko Slaskie S.A. crude lead is produced from sulfide and oxide Pb-Zn concentrates in ISP process. Orzel Bialy S.A. and Baterpol Ltd. produce crude lead in short rotary furnaces in the process of smelting products of mechanical battery scrap separation– desulfurised or not desulfurised paste and metallic fraction. KGHM Polska Miedz S.A. and IMN Divison in Legnica produce crude lead in rotary furnaces in the process of smelting of polymetallic dusts and slimes from copper production processes."

Jan 1, 2008

By Ibrahim Yusufoglu, Cem Kahruman, Sedat Ilhan, Ahmet Orkun Kalpakhi

"Scheelite is the main raw material in tungsten production. In hydrometallurgical processes, extraction of tungstate ions into solution is very important. During the leaching of scheelite in oxalic acid solutions, tungsten dissolves as a chelate complex. Scheelite includes impurities along with calcium tungstate. Determination of the dissolution of these impurities is important in the subsequent tungsten production stages. In this study, scheelite was dissolved in oxalic acid solutions and the dissolution of impurities was investigated. The quantities of dissolved impurities were determined by ICP - OES and characterization of the undissolved impurities in the leach residues was carried out by SEM - EDS analysisIntroductionScheelite and wolframite ores are used for the industrial production of tungsten. Both ores are dissolved in acidic or basic solutions, and ammonium paratungstate is obtained as an intermediate product. Prior to crystallisation of ammonium paratungstate, all the impurities must be removed. Among these, Fe, Si, P, Mn, Mg and Mo are classified as ""harmful"" elements and different methods are used for their removal [1]. During purification, solvent extraction, ion exchange, etc. methods are used.Potashnikov et al. [2] studied the dissolution of scheelite in acidic solutions and the effects of stirring speed, temperature and oxalic acid concentration on the dissolution kinetics.There are no works in the literature about the removal of impurities from scheelite ores in oxalic acid solutions. Therefore, the aim of this work was to investigate the dissolution mechanisms of impurities during the leaching of scheelite in oxalic acid solutions. The effects of temperature and oxalic acid concentration on the dissolution were also investigated. In addition, the characterization of the impurities which were not dissolved was studied."

Jan 1, 2012

By John Jiang, Yeonuk Choi, Olivia Wang, Gus Van Weert

"As part of a general review of processing double refractory ores through Barrick Gold's autoclaves/CIL facility at Goldstrike, Nevada, blanking the gold cyanide adsorbing native carbon in the ore with hard (m.p. >55°C) paraffin wax was proposed. To avoid interference from other ore constituents in the exploratory testwork, commercial activated carbon was substituted for native carbon in the ore to establish the best conditions for de-activation of carbon with molten wax.IntroductionDouble refractory gold ores present two barriers to gold extraction. The first is generally a physical barrier: the gold is encapsulated or dispersed in a matrix which is impervious to the gold lixiviant. In most cases, including the Goldstrike deposit, this involves a pyrite or arsenopyrite matrix, although minor gold may also be dispersed in competent silica (quartz) or iron oxides. Gold can be rendered accessible by oxidative destruction of such sulphide matrices. At Goldstrike this is practised by roasting and autoclave oxidation (POX). It is the latter route to which this paper refers.The second barrier refers more correctly to gold recovery. Gold may be extracted from the autoclave oxidized solids with cyanide, forming a gold cyanide complex. One characteristic of this complex is that it adsorbs on graphitic surfaces. This behaviour is used advantageously on a large scale by gold millers, who use man made activated carbon particles to remove the gold from solution during leaching: the Carbon-In-Leach, or CIL process. The gold bearing carbon particles are larger than the ore solids and can be separately recovered by screening. Goldstrike uses the CIL technology to recover gold after autoclave oxidation."

Jan 1, 2012

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 S. Yokoya

With increasing requirement of steel productivity and quality in continuous casting in the conventional casting system using an immersion nozzle, it is very difficult to establish a reasonable molten flow pattern. In order to overcome this difficulty, we propose a new method of imparting swirling motion onto the flow in the immersion nozzle and to control the flow pattern in the mold. Following results have been obtained during the studies. For the case of slab continuous casting mold: High amplitudes of oscillation with a period of 10 to 15 seconds are observed in the outlet flow of the immersion nozzle and meniscus flow in the conventional casting system, while these phenomena are remarkably suppressed using swirling motion in the immersion nozzle, which leads to very calm and uniform flow pattern at the outlets of the immersion nozzle, in the mold and on the meniscus in the mold; For the case of billet continuous casting mold: (1) heat and mass transfer near the meniscus can be remarkably activated compared with a conventional straight type immersion nozzle without swirl, and (2) Quite different mold flow patterns are observed between the divergent and straight immersion nozzles. Heat and mass transport in the mold using the divergent nozzle is much more reasonable compared to that of straight nozzle. The findings, mentioned above, are very useful to control the flow pattern in the slab, and billet continuous casters. Such effectiveness of swirling flow in the SEN on the mold flow has been put into practical use. As a result, remarkable progress on the quality and production of continuous casting products has been observed in practical application.

Jan 1, 2006

By Han-Tao Hu

Keywords: RH refining process, flow of molten steel, two-phase flow, gas holdup, circulation rate, mathematical modeling A three-dimensional mathematical model for the flow of the molten steel in the whole degasser during the RH refining process has been proposed and developed with considering the physical characteristics of the process, particularly the behaviors of gas-liquid two-phase flow in the up-snorkel and the momentum exchange between the two phases. The fluid flow fields and the gas holdups of liquid phases and others respectively in a 90 t RH degasser and its water model unit with a 1/5 linear scale have been computed using this model. The results showed that the flow pattern of molten steel in the whole RH degasser could be well modeled by the model. The liquid can be fully mixed during the refining process except the area close to the free surface of liquid and zone between the two snorkels in the ladle, but there is a boundary layer between the descending liquid stream from the down-snorkel and its surrounding liquid, which is a typical liquid-liquid two phase flow, and the molten steel in the ladle is not in a perfect mixing state. The lifting gas blown is rising mostly near the up-snorkel wall, which is more obvious under the conditions of a practical RH degasser, and the flow pattern of the bubbles and liquid in the up-snorkel is closer to an annular flow. The calculated circulation rates for the model unit at different lifting gas rates are in good agreement with the determined values.

Jan 1, 2005

By Chikabumi Yamauchi, Mitsuru Tanahashi, Tsuyoshi Taniguchi, Nobuo Furuta, Toshiharu Fujisawa

"It is essential to clarify the equilibrium relations among nonmetallic inclusions of the Mn0-SiO2-CrOx system and molten stainless steel in order to control non-metallic inclusions formed by the deoxidation of stainless steel with silicon. In the present study, the phase equilibria of the MnO-SiO2-CrOx system were measured by conducting the following experiments under controlled oxygen partial pressure, Po2, at 1873 K:1) Phase equilibria of the MnO-Cr20 3 binary system were measured for Po2 = 2 x 10-6 ~2 x 102 Pa.2) Phase equilibria of the MnO-SiO2-CrOx ternary system were measured for Po2 = 2 X 10-6 Pa.Based on the results, the phase diagram of this ternary system was established under the condition of the Si-deoxidation process of stainless steel (Po2 = 2 x 10-6 Pa and T = 1873 K).IntroductionAt the deoxidation stage in steelmaking process, generally multiple deoxidizers participate in deoxidation reactions, and the composition of deoxidation products ""non-metallic inclusions"" greatly varies depending on deoxidizing efoments and their contents. In order to control non-metallic inclusions formed by the refining process of steel, it is essential to clarify the equilibrium relations among non-metallic inclusions and molten steel.Especially, during the refining process of stainless steel, nonmetallic inclusions in molten steel seem to- change as follows. After the oxidation refining, Mn-chromite is formed in molten steel as non-metallic inclusion. By the deoxidation with silicon addition (mainly less than 1 mass%), Mn-chromite inclusions are changed their compositions to Mn-silicate. Segawa et al.[l] have reported the effect of amount of silicon addition on composition and mass ratio· of non-metallic inclusions during the Sideoxidation process of 18Cr-8Ni stainless steel at 1873 K, as shown in Figuri; L At higher silicon content than 0.5 mass%, only Mn-silicate was identified as non-metallic inclusion. On the other hand, at lower silicon content, both of Mn-chromite (MnO Cr2O 3) and Mn-silicate were identified. However, the thermodynamic and the kinetic analyses of the above-mentioned Sicdeoxidation process have not been made due to lack in the thermodynamic data for the non-metallic inclusions· of the MnO-SiO2-CrOx system, such as the phase diagrams, the activities of the components, and the free energy of intermediate compounds. In relation to the phase diagram of this system, those of the MnO-SiO2 [2] and the SiO2-Cr2O 3 [3] binary systems have been only reported"

Jan 1, 2000

By Bora Derin, Sertac Yazici, M. Seref Sonmez

"In this study, the recycling conditions of waste liquor obtained after the production of tungsten boride powder from calcium tungstate by self-propagating high temperature synthesis (SHS) and the following hydrochloric acid leaching were investigated in detail. Environmentally unfriendly and extremely acidic (pH~ -0.3) liquor consisting of calcium, magnesium, and boron ions was treated with 1 M sodium carbonate solution to precipitate magnesium carbonate and calcium carbonate phases. The obtained amorphous precipitates were heated up to the temperature of 400°C for re-crystallization. As a result, MgO, CaC03 and CaMg(C03)z phases were obtained, while sodium, boron, chlorine ions were remain in the solution. The present study is still in progress.IntroductionSelf-propagating high temperature synthesis (SHS) is one of the techniques used in the production of a variety of advanced ceramics, inter-metallic, organic and inorganic compounds, oxygen free single crystals, and polymers [ 1, 2]. The reaction becomes selfsustaining and propagates in the reactant mixture, after initiation in SHS process. SHS products may contain the mixture of several unwanted compounds and elements. Therefore following acidic leaching process may be needed to purify the target product. In the previous study, calcium tungstate (Ca W04), magnesium (Mg) and boric acid (B20 3) mixture were reacted to produce tungsten boride powder by SHS process according to the Reaction 1. Then, magnesium and calcium containing byproducts (i.e. MgO, Mg3B206 and Ca3B206) found in the SHS product were leached out by using concentrated hydrochloric acid (HCl) solution to obtain pure tungsten boride powder [3].Ca W04 + 0.5B203 + 4.5Mg = WB + 4.5Mg0 + Cao (1)After the leaching, filtrate solution consisting of different amounts of magnesium, calcium, and boron requires additional treatment for the environmentally acceptable disposal.Several works were carried out about magnesium precipitation conditions and kinetics from brines. Rabadzhieva et al. investigated the precipitation of Mg(OH)z from brines by using NaOH as well as caustic soda [ 4]. Turek ve Gnot investigated the precipitation efficiency of Mg(OH)z for the temperature range between 10-40°C, while the reaction was kinetically experimented by Alamdiri et al [5, 6]. Homogeneous precipitation of nesquehonite (MgC03.3H20) by the reaction of MgCli with (NH4)2C03 in supersaturated solutions and factors that influence the precipitation of MgC03.3H20, such as reaction temperature, initial concentration, stirring speed, titration speed, equilibration time, have been studied by Wang et al [7]. The precipitation of Mg(OH)z by calcium hydroxide from aqueous solutions was studied by Baird et al. [8]. Stratful et al. focused on conditions influencing the precipitation of magnesium ammonium phosphate from wastewaters [9]. 1031"

Jan 1, 2011

By José Antonio, Silva Souza, Luis Alves Venancio, Emanuel Negrão Macedo, Antonio Ernandes M. Paiva

"The production of alumina from bauxite using the Bayer process generate 1.25 ton of the residue known by red mud and 460 kg of CO2 per ton of alumina.The direct use of exhaust gases from the alumina refineries to react and neutralize the bauxite residue may allow a double gain: open a wide range of new applications for bauxite residue reducing the reactivity of red mud and sequester approximately 15% or 67 kg of CO2 per ton of alumina.This paper shows the reaction of a suspension of bauxite residue-water with a simulation of the calcinator exhaust gases of the refinery. The influence of the temperature and the ratio water red mud is also analyzed.2 IntroductionThe production of millions of tons per year of alumina around the world generates around 1.25 tones of the residue known as red mud and 0.4 ton of CO2 per ton of alumina . The vast majority of the red mud is stored in large sealed lakes. Due to the high reactivity is considered dangerous and currently there is no operating process capable of reuse all the material at any refinery. These lakes after filled of solid material eventually have the surface revegetated. Otherwise will need monitoring for decades and remain as an environmental passive. The search of a industrial process that combine the reduction of the CO2 emission and the reduction the pH of the red mud opening the possibility of use in large scale in a economically viable way is the main objective of this work.The use of the exhaust gases of the refineries to neutralize the bauxite residue may allow a double gain: Open a large array of new applications for the residue with the reduction of its reactivity and sequester million of tones of CO2 plus other gases like SO2 [7] and NOx.This project main objective is to study the reaction of the CO2 with the Bayer process residue in order to obtain the basic parameters to design an equipment capable of process this reaction on a pilot scale. With this objective compositions of red mud on spray were processed with flow of gas containing CO2 at different temperatures and with concentration similar to the exhaust gases of the calcination process of the refineries. With the results, basic concepts of a pilot scale equipment were evaluated.A revision of the work already done on this type of residue were done [3, 9, 10]. Alternatives and potential barriers on chemistry and environmental fields were discussed. With the objective of industrial application the potential use of these materials were evaluated through the pH control, mass balance and x-ray diffraction."

Jan 1, 2010