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By Nils Eivind Kamfjord, Mari K. Næss, Gabriella M. Tranell

"In oxidative ladle refining (OLR) of silicon, the metal surface is oxidized resulting in the formation of a condensed silica fume (SiO2). In the current work, industrial measurement campaigns were performed aiming to measure the fume generation during OLR. A thorough discussion of the possible mechanisms has been included in order to improve our understanding of the Si(1)-O2(g) system.The measurement campaigns were performed at the Elkem Salten plant in Norway. In addition to fume generation from OLR, the metal temperatures and ladle purge gas amount were recorded. The results of this work suggest that fume generation during OLR results from splashing of the metal and/or oxidation of the metal surface, with oxygen transport to the metal surface being the limiting factor. Other mechanisms of SiO2 formation were investigated, however insignificant.IntroductionOne of the main environmental and economical challenges facing the metallurgical industry is fugitive emissions of both materials and energy. In the production of metallurgical grade silicon (MG-Si), refining of the silicon generally takes place through an oxidative ladle treatment (purging with an air-O2 mixture). In the refining process, exposure of silicon to air results in the formation of condensed silica fumes (SiO2) – one of the main sources of fugitive emissions in silicon production plants. The oxidation of liquid silicon, as opposed to solid silicon, has not been widely studied and described in the literature [1], thus a thorough investigation of the oxidation mechanisms, and factors affecting the oxidation reaction rate are essential in order to deal with the problem. In the current work, the rate of liquid silicon oxidation has been studied through industrial measurements of fume generation from refining adles, where the purge gas rate and composition have been varied. The results from these measurements were discussed in light of existing models describing the liquid silicon oxidation kinetics."

Jan 1, 2011

By K. Murayama, M. Kawakami, T. Takenaka, S. Yokoyama

"Cokes play an important role of spacer in blast furnace. However, they degenerate during Boudouard reaction. Blast furnace cokes are reacted with pure C02 at I 072 to 1673 K. Reaction rate was obtained by the weight change of spherical specimen. The specimen after reaction was examined by microscopic observation. The reaction rate increased with temperature and was expressed by two Arrhenius type lines. The activation energy was 126 KJ/mol at higher temperature than 13 73 K and 202 KJ/mol at lower temperature range. At the higher temperature range, the reaction proceeded from the surface leaving unreacted core, whereas homogeneously whole inside at lower temperature. The porosity increased from the center to surface at higher temperature, whereas it was almost constant at lower temperature.IntroductionThe cokes have the function of fuel, reductant and spacer to keep gas and liquid flow in the blast furnace. Thus, the reaction mechanism of coke with several gas and the strength after the reaction should be important factor to control the blast furnace operation. The reaction mechanism of coke with C02 has been studied extensively. The rate equations were derived by Gadsby[ I], Ergun[2] and Turkdogan and Vinters[3]. They were compared and discussed by Kobayashi and Omori [ 4]. Effect of crystallization degree on the reaction rate was examined by Kashiwaya and Ishii[5]. Catalytic enhancement effect of ash componets have been clarified by Kashiwaya et. al. [6]. Although degradation of coke in blast furnace has been examined recently[7], however, the degradation of coke after the reaction with C02 has not been well clarified yet. In the present work, the metallurgical coke specimen was heated in N2 and C02 and the reaction mechanism and degradation behavior after the reaction was investigated."

Jan 1, 2000

By R. Y. Wan, S. L. Chryssoulis

"Gold associations were established in a·biooxidized, chlorinated CIL residue assaying 0.02 oz Ault and in a biooxidized thiosulfate leach residue assaying 0.01 oz Au/t. A detailed mineralogical study involved: assays of screened fractions; light microscopy; ion probe microanalysis to quantify 'invisible' gold in sulfide minerals; proton probe microanalysis to detect and quantify preg-robbed gold. In the CIL residue, most of the gold is preg-robbed (71 %). In the thiosulfate leach residue, gold occurs mainly as submicroscopic disseminations in microcrystalline quartz (chert). In both residues, the 'invisible' gold in pyrite accounts for a minor fraction of the gold assay. Quantitative determination of the gold occurrence in the two residue samples established conclusively that gold adsorption on carbonaceous matter in the thiosulfate leach is of minor importance.Acknowledgement: published with permission of Newmont Gold Company."

Jan 1, 1997

By Bing Gao, Zhe Wang, Xiangdong Xing, Xueqi Zhang, Shan Ren, Jianliang Zhang

"In sintering, the flame front speed (bed permeability) and sinter qualities are greatly depended on the feed size, especially coke breeze and limestone particle size. It is well known that coke breeze provides sinter bed with heat to meet the demand of partial fusion and diffusion bonding while limestone reacts with iron ore to generate bonding phase in the sintering process. Accordingly, it is necessary to find the optimum combination of different particle size of coke breeze and limestone to yield sinter associated with better qualities. In this study, sinter was produced in the sinter pot with varying coke breeze and limestone particle size together in sintering of a coarse hematite iron ore. The sintering productivity was measured and all of the result sinters were examined by microstructure analysis and reduction degradation test (RDI test). For the sintering of a coarse hematite iron ore, it was found that the optimum mean particle size combination of coke breeze and limestone was 1. 71mm and 1.55mm in the sinter mix. On such a circumstance, sintering productivity was higher and the properties of sinter were better.IntroductionNowadays, as the main iron bearing burden material of modem blast furnaces, sinter has a great influence on the blast furnace operation. Sintering is a greatly complex process involving various chemical reactions to form kinds of mineral phases [1, 2]. In the sintering process, coke breeze is used for fuel and it generates heat to raise the green bed temperature. Limestone serves as flux and it reacts with iron ore to produce various mineral phases. On one hand, during the sintering process, the particle size of coke breeze can have an effect on temperature, atmosphere, the flame front speed and all of them act on the microstructure and mineral constitutions of sinter [3, 4]."

Jan 1, 2013

By C. Liliane Carvalho

In the current study, bio-oxidation tests were carried out in shaking flasks with a flotation concentrate containing the sulphides pyrite, arsenopyrite and gudmidite. The tests were performed with mesophilic microorganisms (At. ferrooxidans) at 30 °C and also with the moderate thermophile S. thermosulfidooxidans, at 50 °C. The effects of (i) previous adaptation of the microorganisms to the concentrate, (ii) ferrous iron concentration and (iii) pulp density (2%, 4% and 6% (w/v)) on the dissolution of the sulphide were studied through arsenic extractions. S. thermosulfidooxidans was more sensitive to the pulp density in comparison to At. ferrooxidans as a reduction in sulphide oxidation was observed with the increase in the solid content to 6%. Therefore, the mesophilic strain was selected for further work, which comprised a rolling bottle experiment at 10% solids. After 40 days of bio-oxidation, the solid material was subjected to cyanidation, which revealed 85% gold extraction as compared to 21% from the original concentrate. The antimony sulphide grains in the bio-oxidized product showed similarity to what was observed in the original sample, suggesting such particles were not susceptible to the bio-oxidation process.

By W. G. Davenport

Chapter 13 evaluated the %02 in blast, industrial oxygen and oil requirements for smelting FeSrCuFeS2 concentrates~ This chapter examines high eu grade CU2S-CuFeS2 concentrates the same way.

Jan 1, 2001

By Y. Fautrelle, F. Felten, O. Metais, Y. Du Terrail

"We deal with the prediction of electromagnetically-driven turbulent flows by means of a Large-Eddy- Simulation method (LES). The model is applied in the case of a liquid metal pool submitted to a polyphase linear electromagnetic stirrer. We investigate two cases: (i) the frequency of the magnetic field is equal to 50 Hz; in that case the effects of the pulsating part of the Lorentz forces may be neglected; (ii) the frequency of the magnetic field is low (f= 1 Hz), then the oscillating part of the electromagnetic forces is taken into account. The LES predictions agree well with the mean velocity measurements, as does the standard k-a model. However, as for the turbulent kinetic energy predictions, there is a large discrepancy between the two models. When the oscillating part of the Lorentz forces is taken into account, the computations show that the fluid flow is sensitive to the unsteady part of the forces. We find that the mean velocity is not affected by the fluctuating component of the force. As for the turbulence parameters, the presence of the pulsating part leads to a significant reduction of the turbulent kinetic energy, whilst the turbulence length scale decreases.IntroductionElectromagnetic stirring is commonly used in various metallurgical processes. In continuous casting for example, it may improve the structure of the solidified metal products. Fluid flows generated by electromagnetic stirrers have been extensively investigated (1 ). As for numerical predictions, many works have been published on the subject. In most of the previous works, onepoint closure models have been used. The most used model is the well-known k-i:: model. Those models yield fairly good results as for the mean velocity prediction. However, it has two main drawbacks:(i) the turbulence is not predicted accurately,(ii) it is not well fitted for unstationary flows as well as transitional turbulent motions, where theReynolds number is moderate."

Jan 1, 1999

By E. J. Peterson

Oil shale retorting induces mineral and chemical reactions to occur on the macroscopic and microscopic levels in the kerogen-bearing marlstone. The nature and extent of the reactions is dependent upon process variables such as maximum temperature, time at temperature, atmosphere, and raw shale composition. This report describes the investigation of the mineral, chemical, and trace element release properties of spent shales retrieved from an experimental in situ retort at Occidental Oil Shale, Inc. 's Logan Wash site in Garfield County, Colorado. Correlation between mineralogy of the spent materials and the mobility of major, minor, and trace elements are indicated, and relationships with important process parameters are discussed. The progress .of carbonate decomposition reactions and silicat ion reactions is indicative of the processing conditions experienced by the shale materials and influences the mobility of major, minor, and trace elements when the solids are contacted by water. Shale minerals that are exposed to the extreme conditions reached in underground retorting form high temperature product phases including akermanite-gehlenite and diopside-augite solid solutions, kalsilite, monticellite, and forsterite. The persistence of relatively thermally stable phases, such as quartz, orthoclase, and albite provide insight into the extremes of processing conditions experienced by the spent shales. Leachate compositions suggest that several trace elements, including vanadium, boron, fluoride, and arsenic are not rendered immobile by the formation of the high-temperature silicate produce phase akermanite-gehlenite.

Jan 1, 1981

By Patrick R. Taylor

A novel method for Chemical Vapor Infiltration (CVI) using plasma technology is proposed, Plasma Enhanced CVI (PE-CVI). Due to the low rates at which CVI is currently performed, the use of plasma as a source of heat may be considered to be a faster and less expensive production method. Precursors fed in the hot region of the plasma gas are completely vaporized and forced by the same flow through a porous preform where it condenses as a new material. In this research, silica and methane where used as precursors to form SiC/on a / graphite felt (preform). To enhance the infiltration process, vacuum was used to increase the flow through the preform. Characterization of infiltrated graphite was perfontied using Scanning Electron Microscopy (SEM) and X-Ray Diffraction (XRD). A uniform distribution of Sic was observed along the felt with only twenty minutes of infiltration process, yielding a 178% increment in weight.

Jan 1, 1997

By Y. Suzuki, J. Nagao, Y. Ueda, K. Shimokawa

"A Ti- Ni intermetallic compound could be formed rapidly from Ti and Ni powder compact with SHS process. Microgravity experiments using a drop shaft are carried out, This report shows the effect of microgravity or high gravity on formability of an intermetallic compound. It is concluded that the specimen forms a porous and nearly amorphous alloy by rapid cooling under microgravity but with rapid cooling under high gravity after microgravity, the specimen forms a uniform and dense structure with better crystallinity.IntroductionTi - Ni inter1etallic co1pounds have been produced and have beco1e si1ilar to the a1orphous and porous structure as a result of the SHS (Self Propagating High-te1perature Synthesis) process under 1icrogravity. SHS process is being applied to the synthesis of cera1ics and inter1etallic co1pounds (1). The technique is characterized by a large a1ount of heat being emitted within a very short ti1e interval as regards the sistering reaction. One SHS process, acco1panying 1elting by a reaction was observed, and that was due to the quick heating of a Ni-Ti co1pact containing 50 ato1ic percent of Ti under a low pressure (2-4). In this report, we have researched the use a drop shaft which is 1ore effective during a short ti1e under 1icrogravity and high-gravity, so as to obtain high dense speci1ens with the exception of porous specimens (5). Mechanical properties of each specimen were esti1ated from these 1icro-structures with a discussion about the effect of changing gravity regarding 1elting and solidification of the Ti-Ni intermetallic comounds."

Jan 1, 1996

By A. R. Udupa

The reduction roasting behavior of chalcopyrite has been investigated using various combinations of a desulfurizing agent, i.e., CaO or Na2CO3, and a reductant, i.e., CO, H2 or C. Using these, combinations the sulfur is removed from the mineral as CaS or Na2S rather than SO2 as is the case with conventional copper smelting and converting. The laboratory reduction ex¬periments were conducted using thermogravimetric analysis (TGA) and boat tests of mixed combinations of fine particulate reactants subjected to a continuous gas stream. The degrees of metallization were determined by both weight loss and chemical analysis methods and the products examined using optical and scanning electron microscopy and electron probe microanalysis. The percent reduction after one hour at 900°C ranged from 60% to 94%. From these data It was possible to provide postulations as to the controlling reduction mechanisms.

Jan 1, 1983

By Li Xi

This paper describes how a back-propagation neural network is built for predicting the properties of engineering materials from their other properties, compositions or processes. A predicted result of the impact toughness of a 12Cr-2Ni-1.5Mo stainless steel from its tempering temperature is presented. Furthermore, the combination of this neural network for prediction is able to supplement the unpredictability of the expert system outside its domain of expertise. An integrated system may perform more intelligently and solve more complex problems as well as human expert, in some case even better.

Jan 1, 1992

By Z. Zak Fang, P. Fan, S. Middlemas

"Titanium dioxide (T1O2) has been widely used as pigment in paints, paper and cosmetic products, as well as high-tech applications such as PV Cells, semiconductors, biomedical devices and air purification. T1O2 pigment is primarily produced by the high temperature chloride process, resulting in considerable CO2 emissions. A novel hydrometallurgical process for making T1O2 pigment without direct CO2 emission is investigated. The new method promises to eliminate direct CO2 emissions, consume significantly less energy, and produce minimal environmental waste. The novel process involves molten salt roasting of titania slag, with subsequent washing, leaching, solution purification, hydrolysis, calcination and post-treatment stages, resulting in high-purity anatase or rutile pigments while realizing significantly reduced environmental impacts. Pigment whiteness is critically sensitive to trace amounts of discoloring impurities such as iron and chromium. Several methods for reducing the levels of these impurities are investigated. Energy consumption and emission models are also developed.IntroductionTitanium dioxide (T1O2) is one of the most commonly used minerals in the chemical manufacturing industry. It has been commercially processed since the early 1900's, and has a wide variety of applications. Pigment is used in paints [1], plastics and paper [2], sunscreen [3], cosmetics and even as a food additive [4]. T1O2 has also been used in photovoltaic cells [5], biomedical devices [6], and in air purification [7]. T1O2 pigment has a refractive index of 2.7, which imparts a high level of opacity (and hence whiteness) to whatever material it is added [8]."

Jan 1, 2012

By R. Hamar, G. Lamanthe

"To realize complex shaped pieces, like turbine blades, superalloys are cast with the lost-wax process. The end properties of these parts depend upon their microstructure as well as upon the occurence of casting defects such as micropores and hot tears. Such features are governed by the local solidification conditions which may be describe by the calculation of thermal transfers between alloy and mould. It needs the evaluation of numerous parameters which are fitted from experimental measurements in real castings. In further simulations, any parameter may be changed, in order to determine its influence. Such a single modification is quite impossible to realize in real castings, which shows that numerical modeling is a very good way to study casting processes.This modeling technique of casting is applied here to the real study of a typical low pressure turbine blade of a civil engine.IntroductionAircraft engine manufacturers use superalloys to produce turbine blades. They have to obtain a given microstructure and to avoid solidification defects to give good mechanical properties to theirs castings. For example, microporosity is induced by a large shrinkage that cannot be completely fed with the remaining liquid alloy .The optimization of casting processes needs a good Knowledge of the solidification process, that must be controlled at every place in the casting, and at every time of its freezing. Material and heat transfers that occur during the solidification, can be estimated from rather complex calculations. To model these physical phenomena, the evaluation of many parameters must be made. In this aim, some casting experiments are fitted with numerous thermal captors. The identification of experimental and computed thermograms let us estimate these parameters.A long-range scientific cooperation between SNECMA and INPG has enabled the realization of such studies on this topic. From all of them, this paper describes an experimental and computed investigation which has been led on a typical low pressure turbine blade of a civil engine."

Jan 1, 1986

By Sang-Beom Lee

For thermodynamic prediction, the deoxidation equilibrium of aluminum in Fe-36%Ni alloy was studied with a cold crucible under Ar gas atmosphere at 1773K. For the deoxidation reaction in liquid Fe-36%Ni base, i.e.: A12O3(s) = 2A1 + 3O The interaction parameters and the equilibrium constant between aluminum and oxygen in liquid Fe-36%Ni alloy are given in the following: eo Al = -3.8, roA1=0.9, eAl° = -6.4, rAl° = 700, rAIAIo = 3.1, roA1o = 833 within the composition range of [Al] < 1 mass%. The temperature dependence of the equilibrium constant was obtained in the range of 1773K < T < 1973K by using reported data and present results as follows: log KAo= 0.58-24463.7 / T The deoxidation equilibrium with aluminum in Fe-36%Ni could be thermodynamically well described in the range up [Al] < 1 mass% with first and second order interaction parameters as well as the equilibrium constant determined in this study.

Jan 1, 2002

By Ximena Diaz

Mercury is one of the most undesirable contaminants in gold bearing ores. During cyanidation mercury cyanide compounds accompany gold in all the extraction and recovery processes. Of course mercury in the carbon eluates creates environmental problems in subsequent refining steps. One possible process alternative for the separation of gold from mercury in such concentrated alkaline cyanide solutions is the selective solvent extraction of gold by undiluted Dibutyl Butyl Phosphonate (DBBP). In order to describe the behavior of mercury during extraction by DBBP, the results from a preliminary research program are presented. In this study, temperature and cyanide concentration have been found to be the most significant variables which influence the separation of gold from mercury by solvent extraction using DBBP. It was found, using plant eluate from a carbon strip, that excellent separation of gold from mercury can be obtained at 60&apos; C with 98% gold recovery and complete mercury rejection in a single stage of extraction. The influence of pH is also discussed in terms of the extraction chemistry. These results complement previous research which described the DBBP solvation extraction of an aurocyanide ion pair. In addition, these results extend our understanding of the alkyl phosphorous ester extraction systems by illustrating that neutral ionic species such as Hg(cN)02sq, can be extracted at low cyanide concentrations, a phenomenon which had not been observed previously for other cyanoanions.

Jan 1, 1993

By Kiyoshi Takai

The Para-Eco Incinerator Ash Processing System for cleaning slag has been developed after a seven-year pilot plant study. The major part of the system is an electric furnace heated to 1773 K. The feed material consists of a municipal solid waste incinerator ash mixture containing a reducing agent of a coke and an inorganic flux of calcium and magnesium. With this furnace system, three kinds of products are produced. They are an inorganic molten salt that is slag, molten iron alloy absorbing non-ferrous metals, and fly ash. Due to the reducing atmosphere in the furnace, the slag does not contain any metal components as well as chlorine components just like natural rock and/or aggregate. A retreatment plant modifies this slag into a practically useful aggregate. The plant consists of a slow cooling step for crystallizing the slag as well as a water granulation step. The iron components in the ash are reduced to molten iron droplets, which concentrate at the furnace bottom. The non-ferrous metal components such as copper, chromium, and others are absorbed into the molten iron but not into the molten slag. Volatile metals such as lead, zinc, cadmium and others as well as sodium, potassium, and chlorine go back into the fly ash. A solvent extraction method and/or other appropriate procedures can be used to extract the metal components from this fly ash.

Jan 1, 2003

By G. Gao

Flyash from municipal solid waste (MSW) incinerators is frequently classified as a characteristic hazardous waste due to its lead and cadmium content. Extensive investigation has therefore been carried out to detoxity the flyash by leaching and to recover lead, cadmium and zinc. Detoxification can be accomplished by leaching in HCI/NaCI solutions. Optimization of leaching conditions for effective detoxification and subsequent metal recovery can be achieved by controlling the acidity of the lixiviant and flyash to lixivaint ratio. Lead and cadmium In the leaching solution is recovered by cementation with zinc dust. Leaching and cementation experiments have shown that zinc concentrations suitable for electrowinning, > 15 g/liter, can be achieved. Experiments have also been performed to determine the effects of pH, particle size of the zinc dust used, quantity of zinc added and dissolved impurities on the cementation kinetics. After recovery of lead and cadmium, electrowinning or electrowinning coupled with solvent extraction can be used to recover zinc. A process flowsheet is presented.

Jan 1, 1991

By T. T. Chen

Kidd Creek continuously-cast copper anodes are characterized by high levels of Se, Pb and Ag; the anode slimes constituents and their morphologies are controlled by both the anode composition and the casting process. Hollow Cu2Se spheroids and tube-like structures, enveloping Cu-Pb-As oxide and/or Cu2O, are present in the as-cast copper. During electrolysis, the selenides are liberated from the copper and accumulate in the slimes layer; the Cu2O and Cu-Pb-As oxide react rapidly with the electrolyte to form soluble species and PbSO4. Silver, which is present mostly as a solid solution in the anode copper, is also liberated during electrolysis and reacts with the Cu2Se to form (Cu,Ag)2Se. The ultimate composition of the selenides in the slimes layer depends mostly on the Ag and Se contents, but various other elements, including Au and Te, are also structurally incorporated. Although the selenides are the major Ag carrier, metallic silver also is present. A thin layer of Cu2O crystals sometimes forms at the copper surface, and may affect anode passivation. Copper sulphate is a common constituent and serves to agglomerate the slimes. Copper sulphate is present on both passivated and non-passivated anodes, but that observed on the passivated metal is present as a thick compact layer. Copper powder is associated with CuSO4.5H2O only on passivated surfaces.

Jan 1, 1987

By Asmo Vartiainen

The viscosity of liquid Fe-O-SiO2 -slag at copper smelting conditions was investigated using a rotational viscometer. The studied parameters were oxygen partial pressure (10" °-10"6 bar ); composition of slag (Fe/SiO2 ratio), and temperature (1250-1400°C). The viscosity values are presented as a function of Fe/SiO2 ratio and as isoviscosity curves in ternary FeO-Fe2O3-SiO2 diagrams. The increase in viscosity at high silica contents can be accounted for the polymerisation effect of SiO4/4- -anions. At high ferric iron contents, higher oxygen partial pressure, the viscosity values increase especially near the magnetite saturation. The viscosity values are highest at the double saturation of silica and magnetite. At lower silica and ferric iron contents the viscosity values are more uniform in the homogenous liquid slag area. The viscosity values were lowest at high temperatures and highest at low temperatures.

Jan 1, 1998