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By S. Niyomwas, R. G. Reddy

"A mathematical model was developed to describe the plasma gas and particle dynamics and conversion yields. The velocity and temperature fields in the plasma were calculated by solving 1 the Navier-Stokes equations and the thermal energy balance equations. Conservation equations for the system species consider the multi-component diffusion and chemical reactions. Through the application of this model, temperature distribution, flow fields, and production rates were computed. The model was used to study the thermal decomposition of ilmenite in the non-transferred arc plasma reactor. The computed production rates of TiN from ilmenite using nitrogen and methane gas mixtures, are in the range of 5 to 100 x 104 kg/m3/s at 2500 KIntroductionThe widespread interest in thermal plasma processing has stimulated a great deal of research effort into the various aspects of this process, including plasma' spraying, thermal plasma chemical vapor deposition, plasma synthesis of fine powders, thermal plasma decomposition, plasma melting, and plasma extractive metallurgy.In the plasma synthesis of fine powders, the earlier experimental and theoretical studies aimed at predicting the final products1-5. Then it was followed by more recent investigation concerning the profile of plasma gas velocity, plasma temperature and concentration. In this regard, useful plasma processing models have been reported by numerous investigation6 -11 which were increased by both theoretical analysis and measurement.As a result of this work a reasonable plasma-processing model is proposed. It is to be noted that all the thermal analysis that has been made neglected the fluid -flow effects. Also, in the analysis aimed at the quantitative description of the fluid-flow field, the effect of heat transfer was not taken into account."

Jan 1, 2000

By K. Adham

For use in many existing and emerging applications, the purification of natural graphite is required to achieve +99.9% carbon content with minimum metallic impurities. Currently, the hydrofluoric acid process is used, which carries certain environmental and workplace health and safety impacts. While thermal purification of graphite at temperatures over 2500 °C is a known alternative, such high-temperature furnaces are expensive to build and operate. Using chlorine at lower temperatures to purify graphite is also known and patented, but is currently limited to treating solid synthetic graphite shapes in small-scale batch furnaces. Chlorine treatment of natural flake graphite resources can be used commercially, if certain drawbacks are addressed through process improvements that can be helped with the use of fluidized bed reactor technology.

By Gaifeng Xue, Lei Zhang, Xia Liu, Lina Wang, Pu Liu, Benquan Fu

"Experiments were conducted to investigate the behavior of the integrated process with a three-dimensional electrode reactor combined with Fenton process for coking wastewater treatment. Effects of initial pH value, reaction time, H20 2 dosage, Fe2+ dosage on Total organic carbon (f OC) removal rate were investigated. The kinetics of degradation of TOC from coking wastewater by three-dimensional fluid bed electrode reactor combined with Fenton process was also studied. Experimental results shows that three-dimensional fluid bed electrode reactor combined with Fenton process had better synergic effect, average 17.4% TOC removal rate was improved within an hour. It was found that TOC degradation in coking wastewater followed a pseudo-first-order reaction kinetic model. The optimum degradation efficiencies of TOC were up to 60% as pH3.4, 3.5 mM ofFe2+ andl.2-1.8ml/L H20 2 in 90min reaction period. Furthermore, the integrated process showed a rapid reaction performance at a low temperature within a short reaction time and remained high efficiencies for TOC removal. Overall, the integrated process was proved feasible for coking wastewater treatment in practical applications.IntroductionCoking wastewater is generated from coal coking, coal gas purification, and by-product recovery processes of coking, which is composed of phenolic compounds, heterocyclic compounds, polycyclic aromatic hydrocarbons, ammonia, cyanide, polycyclic nitrogen-containing aromatics, acyclic compounds, etc. Most of these constituents are refractory, poor biodegradability, toxic and carcinogenic['-31. Currently, coking wastewater is usually treated by different forms of A/O biological nitrogen removal process as the primary treatment process, but the aforementioned processes are not efficient enough to meet the requirements from the National Discharge Standard in China (GB13456-1992). According to the continuous requirement on improving environmental protection for coking industry (revised 2008), increasing wastewater utilization ratio and reducing discharge of effluent in the coke industry has to be implemented for cleaner production and sustainable development. Therefore, advanced technologies need to be developed to treat coking wastewater and reutilize the product as industrial cooling water, which would be one of the best choices to achieve zero discharge of wastewater and reduce water consumption per ton of steel [4-51 . In this study, three-dimensional fluidized bed electrode reactor combined with Fenton process was adopted to advanced treatment of coking wastewater, and the effects of operating conditions, including H2O 2 dosage, Fe2+ dosage, initial pH, and reaction time on TOC removal rate, were investigated. Meantime, study of kinetics of reaction was estimated."

Jan 1, 2013

By D. D. L. Chung

"In-situ network composites are composites in which the filler network is formed during composite fabrication, in contrast to ex-situ networks which are formed prior to composite fabrication. A homogeneous in-situ network composite has the entire network at the same composition; a heterogeneous in-situ network composite has different parts of the network at different compositions. The homogeneous network composite is made either by the Method of Molten Filler Flow or the Method of Dissolution and Deposition; a heterogeneous network composite is made by the Method of Liquid-Phase Networking. Examples include polymermatrix and metal-matrix composites.IntroductionNetwork composites refer to composites containing a continuous three-dimensional network as the filler. These composites are attractive in their lack of delamination failure, which is usually characterised by two-dimensional composites. The filler and matrix in a network composite can be considered two interpenetrating networks. The mechanical interlocking of the networks adds to the cohesion of the composite. In cases where the filer is much better than the matrix in a certain property, the network nature of the filler makes the filler highly effective in improving that property in the composite in all directions. The property desired in the composite may be high strength, high modulus, low coefficient of thermal expansion, high thermal conductivity, or low electrical resistivity."

Jan 1, 1994

By M. A. Cocquerel

External process energy requirements and air pollution control regulations formulated to limit particulate and SO2 emissions are impacting on smelting and converting technologies and the corresponding process and secondary gas handling systems. This paper presents an overview of the different technical solutions used for cooling and dedusting the process gases in the different pyrometallurgical copper concentrate stages, including: drying, smelting, converting, slag cleaning and fire refining. The main principles of the process gas handling systems are presented &d a qualitative technical and economical comparison is discussed in relation to process changes, energy recovery and marketing or disposing of the various sulfur fixation by-products. Finally, a brief review of the methods for fixing sulfur contained in the process and secondary gases is presented.

Jan 1, 1999

By Carlos M. Fontes Vieira, Ruben J. Sanchez Rodriguez, Carlos E. Gomes Ribeiro

"The worldwide demand for ornamental stones in building construction is motivating the use of their wastes, generated during fabrication, to produce compound stones. This work has as its objective to investigate the production of an ornamental compound marble (OCM) under vacuum and compression processing of a polyester matrix composite with addition of marble waste as load and as filler. Square OCM composite plates were subjected to compression and flexural mechanical tests. Samples were analyzed to obtain the density and water absorption. The OCM composites presented properties within the expected range of an artificial stone.IntroductionMarble is a limestone, composed mainly of calcite, more or less crystallized by metamorphism that ranges from granular to compact in texture. It has a density 2.7 g/cm3 and its porosity is approximately 0.4%. The UNI 8458 standard defined marble as: ""every crystalline rock constituted mainly by minerals with a Mohs hardness equal to 3-4"". In marble production around70 - 75% of whole extract material is lost in byproducts generation [1,2].In function of large volume of residues generated, the ornamental stones industry has attracted ever more the attention of environmentalists [3].Actually the marble can be pulverized to obtain calcium carbonate for industrial applications. It is also possible to obtain a thinner powder to produce concretes [l]. Some authors study the use of stone residues in concrete mortars and ceramic bricks, getting better properties to these materials [3,4].The marble residues can be also used in engineered stones, or ''agglomerated"" stones, production. The most common engineered stones in the market consist, like a polymer concretes, in polymer matrix composites incorporating petreous components. In the formulation of the engineered stones, the particulate or granular petreous components are the result of fragmentation or trituration processes to which natural stones were submitted to [ 5]."

Jan 1, 2014

By O. Ryosuke Suzuki

A new metallurgical process via sulfide is proposed: a sulfide is produced at a high temperature from its metallic oxide using gaseous CS2, and this sulfide is electrochemically reduced to its metallic state using molten salt. This combined process via sulfide is effective to obtain high purity of metallic powder, even if the metal in its oxide is strongly combined with oxygen. For example, it is not easy to reduce stable oxide TiO2, and only Ca can remove oxygen to form α-Ti. However, a fairly large amount of oxygen remains as Ti–O solid solution. Because the solubility of S in Ti is very small, this proposal was examined experimentally both on the conversion of TiO2 to TiS2 and on the successive reduction of TiS2 to Ti. TiO2 powder was exposed to CS2 gas flow at 1073 K, and the conversion to TiS2 was confirmed. TiS2 could be reduced to Ti powder either by calciothermic reduction or electrolysis in a CaCl2 melt. By Ca reduction at 1133 K in CaCl2 melt, sulfur concentration decreased to 0.03 mass%S when the amount greater than twice the stoichiometric calcium amount is added. By electrochemical reduction at 1173 K in CaCl2–CaS melt, S concentration significantly decreased to 0.01 mass% S when four times larger amount of electric charge was supplied.

By Vitalij K. Pecharsky

Recent interest in complex aluminohydrides as potential near ambient, ultra-high capacity, solid-state sources of hydrogen (e.g., for fuel cells) calls for an improved understanding of the processes occumng in these hydrogen-containing materials during both the release and the uptake of hydrogen. Lithium aluminohydride (LiAlH4) rapidly releases 5.2 wt. % of hydrogen (i.e., nearly four times more than LaNis-based alloys) during mechanochemical processing at ambient conditions in the presence of transition metal catalysts. Using a variety of solid-state characterization techniques, the mechanochemical transformations in a series of LiAlH4 - metal catalyst systems have been examined and preliminary insights on the mechanism have been obtained. Surprisingly, the well-known hydrogenating-dehydrogenating catalysts, such as Ni and Pt, are practically inactive in the mechanochemical dehydrogenation of LiAlH4.

Jan 1, 2002

By Olli Hyvärinen

The capacity of Outokumpu Pori Copper Refinery has been increased by 50 % to 70 000 t/a in the last five years by adopting periodic current reversal, reducing spacing and installing some new cells in the old tank house building. Five years operation of PCR has proved that it is possible to achieve additional capacity with PCR and yet produce high quality cathodes. The impurity level in anodes has considerably increased, and recently, arsenic, antimony and sometimes bismuth have displaced nickel as the most critical impurity.

Jan 1, 1987

By David B. George

Kennecott Utah Copper adopted Outokumpu Flash Smelting and Kennecott-Outokumpu Flash Converting in 1995, a process based on granulating high grade copper matte. While nickel mattes and very small quantities of copper matte had been commercially granulated for years, no large scale copper matte granulation system had been built. This paper summarizes the history and benefits of copper matte granulation, the Kennecott design basis, the successful operation for over 10 years and potential problems inherent in some matte granulation approaches.

Jan 1, 2006

By Wufeng Jiang, Jiann-Yang Hwang, Suju Hao, Yuzhu Zhang

Lime was made by the calcination of limestone in a high pressure resistance furnace. The lime mineralogical phases and micro-morphologies was characterized by field emission scanning electron microscopy (FE-SEM). The lime activity degree was determined by acid-base titration, and the lime pore distribution was measured by mercury intrusion porosimetry (MIP). The results show that with the increase of calcination pressure, the lime activity degree is increased, and the lime develops a large pore structure. The desulphurization experiments were carried out in the induction melting furnace using active lime with different activity degrees as a desulfurizer. The results show that the desulfurization performance of lime is closely related to the activity degree. There is a strong positive linear relationship between the desulfurization rate and the lime ’s activity degree.

Mar 1, 2018

By Bowen Li, Jiann-Yang Hwang, Mingsheng He, Huaguang Wang

Kyanite is one of the major high-alumina minerals for producing refractory ceramics. At high temperature, kyanite can be decomposed into mullite and amorphous silica. This change is an irreversible decomposition and provides potentials for fiber reinforcement of ceramic matrix. In this study, kyanite powder was compressed into a cylinder green body of ceramic and heated at 1150–1450 °C.The phase transformation of kyanite and sinterability were investigated by X-ray diffraction and scanning electron microscopy. The results showed that the phase transformation of kyanite started at 1150 °C when rising the temperature. At 1350 °C, kyanite is completely converted into mullite and silica. The compressive strength of the ceramics reached 73.3–134.8 MPa, while the bulk density was 1.95–2.47 g/cm3. The microstructure indicated the correspondence of the compressive strength to mullitization degree of kyanite.

Mar 1, 2017

By Jr. Robison

"Aluminothermic (""thermite"") smelting became commercial with the development of tonnage aluminum, and prospered producing metals and alloys with higher cleanliness, consistency and elemental control than competing technologies. We explore the scope of thermite smelting, and metallothermic smelting in general; the thermochemistry of the process; and its advantages and limitations as applied to industrial production. We review currently-produced products of thermite smelting in several forms and a wide range of heat sizes. As these products serve several industries, we relate the demands of those industries to the requirements imposed on the thermite process, leading to process dynamics and mechanisms to control/alter those dynamics. We review ways to lower the process costs by altering process stoichiometry, using other energy sources and utilizing less costly materials while considering effects on product quality and customer requirements. Finally, we examine overall emissions control and waste disposal.IntroductionAluminothermic smelting is the reduction of various oxides by aluminum to produce metals or alloys with varying levels of residual aluminum. One of the earliest uses of the process was the production of liquid iron to weld railroad rails, later modified in ""thermite grenades"" used to ""spike"" artillery pieces in World War II. Then during the 50's, 60's and 70's the growth of jet aircraft created a demand for new superalloys and titanium alloys, both requiring master alloys for efficient production. Aluminothermic smelting grew with the aerospace industry and with the expansion of microalloyed steels. It is very much a niche industry, dependent on the specialized demands of the specialty steel, superalloy and titanium industries. In this paper we introduce the characteristics of aluminothermic smelting, the scope of smelting operations, the markets served, and the environmental aspects of the process, as seen through the eyes of a company using aluminothermic smelting for over fifty years"

Jan 1, 2012

By K. S. Han, M. Yoshimuura, H. Fujita, Y. Sato, S. W. Song

"Film of LlCoO2 as cathode material for rechargeable lithium microbatteries has been fabricated on the platinum metal substrate by electrochemical-hydrothermal method in concentrated LiOH solution at 200 °C as Soft Solution-Processing. The film fabrication has been understood in terms of dissolution of cobalt metal powders and subsequent oxidative deposition on the substrate. The film structure was characterized using scanning electron microscope, X-ray diffraction analysis; X-ray photoelectron spectroscopy and micro-Raman spectroscopy.IntroductionRapid growth of wireless communications and emerging integrated optoelectronic circuits caused the miniaturization· cif electronic devices, thus the demand for high energy density microbatteries as a power source for the microelectronics increases. In this regard, all solid-state lithium microbatteries including LiCoO2 and LlMn2O 4 [l-4], the most promising intercalation cathode material, have been developed. However, major difficulty of .fabrication of a lithium microbattery arose from the preparation of cathode film, according to a· recent report on Rare Metal News [5]. Although many attempts have been made to deposit the cathode films, all those methods are mostly chemical vapor deposiiton (CVD), various evaporation, sputtering techniques and spray pyrolysis. These methods require preparation of bulk cathode materials cir its precursor, then deposition with complicated instruments including high· vacuum system, and even postsynthesis annealing to obtain desire electrochemical 'properties. It is clear that all of these techniques are neither economic nor environmentally friendly. Compared to those methods, film form.ation from an aqueous solution is thought to be simpler and more economical, and requires much· less energy consumption. Our .group has demonstrated the utility of Soft SolutionProcessing [6,7], which is defined as environmentally friendly processing using (aqueous) solutions, to produce films of a variety of functional solid materials. According to the Pourvaix's diagram [8], some metal can be dissolved in an alkaline solution and consequently combined with hydroxyl group or oxygen anion forming metalate or metalite. Cobalt also seemed to form cobaltite, HCoOi in strong alkaline solution in the Pourvaix's pH-potential diagram. Based on this information, it was expected that LiCoO2 could be prepared using the cobalt metal in Li OH solution by Soft Solution-Processing. Recently, we reported the successful single step fabrication of electrochemically active LlCoO2 films on the cobalt metal substrate by hydrothermal methods without any post-synthesis annealing as Soft SolutionProcessing [9,10]. Film formation mechanism could be elucidated by the following evidences. . As expected from Pourvaix's diagram, cobalt metal was dissolved in concentrated LiOH solution forming dissolved cobalt species which was detected by an observation of absorption band in UV-VIS absorption spectrum [10]. Thus the reaction was assumed to be started from dissolution. Time dependent potential of Co electrode exhibited only one-step evolution with 0.6 eV from Co metal to LiCoO2 [10]. Another strong evidence was the finding of LiCoO2 powder precipitates at the bottom of tetlon beaker after the reaction [11]. Based on those experimental findings, it was understood that film is formed by dissolution-precipitation mechanism [9-11]."

Jan 1, 2000

By Donald R. Sadoway

The viability of treating certain forms of hazardous waste by direct electrolysis in molten oxides is under investigation. Secondary residue or waste mud produced in the course of chromate chemical production is the focus of attention in this study. The goal is to reduce the water soluble hexavalent chromium either to insoluble trivalent chromium or to chromium metal. Electrolysis tests have been conducted in a high temperature cell containing chromate sludge dissolved in an electrolyte composed of Al2O3, SiO2, CaO, and MgO. Oxygen production on a carbon-free anode has been confirmed.

Jan 1, 1992

By C. J. N. Buisman

THIOPAQ technology developed and marketed by PAQUES Bio Systems in Balk, Netherlands, has been successfully used at commercial scale at the Budelco zinc refinery in the Netherlands for the treatment of contaminated groundwater since 1992. In essence, THIOPAQ technology consists of two biological process steps in series: sulfate reduction to hydrogen sulfide (anaerobic) and sulfide oxidation to elemental sulfur (aerobic). The biogenic sulfide produced can be employed for the chemical precipitation of metals in solution either inside the anaerobic reactor or in a separate vessel. Since the solubilities of most metal sulfides are much lower than of their respective hydroxides, considerably lower effluent metal concentrations can be achieved with THIOPAQ systems than in neutralization processes which immobilize metals predominantly by hydrolytic precipitation. In recent years, PAQUES has made significant advances in the design and operation of aerobic and anaerobic bioreactors for metal-sulfur systems. Moreover, the company has increased its technology portfolio to allow the development of more process oriented applications of THIOPAQ technology. A new PAQUES designed plant at Budelco treating sulfatecontaining proceswaters will be started up in 1999. The sulfate reduction is accomplished in a 500 m3 reactor in which hydrogen is used as electron donor. The endproduct, ZnS, is used for Zn and H2S04 production.

Jan 1, 1999

By A. Ohno

"A new near net shape casting process, OHNO Continuous Casting (OCC), has been recently developed. In this process, molten metal is fed into a heated mold maintained at a temperature above the solidification temperature of the metal being cast. Solidification begins from the central core of the casting rather than the wall of the mold. With the heated mold, the formation of crystals on the mold wall is prevented and solidification occurs out of contact with the mold surface. This produces near net shaped products with smooth, mirror-like surfaces and unidirectional grain structures free from cavities, porosity and segregation. Any crystals formed at the beginning of solidification decrease in number as solidification progresses and eventually a single crystal product is obtained. This process is applicable to any metal alloys, converting them into new materials with superior properties and quality.IntroductionAs a result of growing technical demands for more advanced and diversified materials, the OHNO Continuous Casting (OCC) technology has found many new applications in industry. Considerable interest in the process has been shown in Japan and other countries because of its distinct ability to:produce a single crystal, (1)produce a remarkably clean cast surface without a witness mark,provide extremely good ductility,and reduce casting defects and segregation.This paper provides an overview of the principle of the OCC process and describes the remarkable characteristics of the material produced by this method."

Jan 1, 1988

By Jay S. Gunasekera

Metal parts are traditionally processed by either filly-liquid (e.g., casting) or filly-solid (e.g., forging) state. Semi-solid metal forming incorporates elements of both casting and forging. In 1991, Gunasekera(5) developed a model illustrating the influence of flow stress by the liquid fraction. The result fits Kiuchi's (1979)(7) experimental data quite well. This model assumed the liquid part is surrounded by solid as small pockets inside the material, which is opposite to the real practical situation. Since the melting usually first happens at the grain boundary, it is better to treat the semi-solid material as small metal crystal surrounded by liquid.

Jan 1, 1997

By Rolando Campos

Until 1970, the Caletones Smelter of CODELCO-CHILE, División El Teniente, operated under the conventional pyrometallurgical process used by most of copper smelters. The annual copper production varied around 165.000 tons. The failure in the commissioning of the "oxygen smelting" technology in Peirce- Smith converters (1970-1972), forced further introduction of transcendental changes in the Caletones smelter operating scheme. Implemented technological innovations were based on wide studies and research works performed by División El Teniente. This paper presents a summary of technological modifications introduced, their impact on production and energetic performances, and short and medium terms improvement plans.

Jan 1, 1993

By Dachun Liu, Lei Shi, Yongnian Dai, Bin Yang, Yang Tian, Tao Qu

The carbonthermal reduction of high Mg–Si nickel laterite was studied under vacuum. The effects of adding calcium oxide and the reducing agent on the reduction of silicon in residue were studied at pressures of 10–200 Pa and different temperatures, with varying proportions of carbon and CaO. The analysis of the residue was performed using X-ray diffraction and chemical composition analysis. The results show the following: At 1350 °C with a C/O ratio of 1.5:1, the recovery of Si reached a maximum 71.09%. Under these conditions, Si exists mainly in the forms of Fe3Si, Fe2Si, FeSi and SiC. The recovery of Si was above 80% when the temperature was 1450 °C, the C/O ratio 1:1, and 15% addition of CaO. When CaO addition was 22.61%, all of the solid phase was Ca2SiO4.

Mar 1, 2017