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By Kanchan Mondal

"Methanol, lower hydrocarbons, CO, and HCOOH formation have been by the reduction of CO2 with H2. Un-catalyzed electro-reduction requires a significant overvoltage. An alternate route has been conceptualized. Production of hydrogen from water can be achieved by chemical oxidation of a metal in water followed by oxidation of the hydronium ion by the released electrons to form hydrogen radical. It is hypothesized that circumventing the problem of the formation of hydrogen molecule is essential while having the hydrogen radical to react with CO2 forming methanol, etc. This may be possible by a bimetallic catalyst acting as a galvanic couple, wherein one metal acts as the electron donor for the production of hydrogen radical while the other acts as a catalyst for the reduction of CO2. This may enhance the reaction rates. The current concept circumvents the need for an external electric field unlike the electrochemical process.IntroductionUtilization of carbon dioxide as a raw material, not only as carbon sources but also as useful chemical feedstock is a more holistic approach to reduce air pollution by flue gases (1-3). Several methods have been proposed to maintain the concentration of atmospheric CO2 or to reduce and recycle it. One of these is the chemical fixations using catalysts. The conversion of CO2 to methanol by hydrogenation over copper containing catalysts is one of the most widely studied subjects in this area. The limitation in this reaction is the low conversion of CO2."

Jan 1, 2008

By Z. Y. Xie

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

Jan 1, 1993

By Byung-Su Kim

The recovery of elemental sulfur from sulfur dioxide has important implications for coal- burning power plants and nonferrous metal smelters. The thermodynamic analyses showed calcium sulfide to be suitable for recovering elemental sulfur from sulfur dioxide. At the temperatures of 1023 to 1153 K under the sulfur dioxide partial pressures of 5.0 - 60.1 kPa, elemental sulfur from sulfur dioxide was recovered by its reaction with calcium sulfide. The kinetics of this reaction were measured at the same conditions using a thermogravimetric analysis technique. This reaction scheme would be attractive if the coproduct calcium sulfate can be reduced to regenerate calcium sulfide. This is the topic of another paper. At 1073 K under the sulfur dioxide partial pressure of 25.8 kPa, 48 % of the original calcium sulfide was converted to calcium sulfate in an hour. Under the same conditions, 55 % of the regenerated calcium sulfide were converted to calcium sulfate in an hour even after third regeneration.

Jan 1, 1999

By Marta Cabral, C. A. Nogueira, F. Margarido

"Physical processing of spent batteries which includes shredding and sieving operation is the first step for chemical treatment by hydrometallurgy. A laboratory study was carried out to evaluate physical processing efficiency, by analysing the resulting particle size, of alkaline and saline mignon-type Zn-MnO2 batteries. After shredding with a tip shredder, results obtained showed that alkaline batteries were more efficiently size reduced than saline batteries. Difference in particle size distribution was larger for granulometric fraction -20+11.2 mm and also higher for saline batteries. Average diameters (d50) for saline and alkaline batteries were respectively 9.1 and 6.2 mm. Chemical composition carried out on several granulometric fractions allowed to identify metals distribution through size categories. This analysis showed that zinc concentration with the grain size was almost constant, while manganese decreased when particle size increased. More than 95% of iron scarp from the battery cases had a particle size higher than 5.6 mm.IntroductionRecycling process of spent batteries includes physical unit operations which involves a fragmentation step in order to open the battery cases and to allow the access of chemical reactants to the electrode materials, on further chemical unit operations. Shredders are usually used for that purpose, using cutting mechanisms and allowing efficient fracture of residues in order to promote further processing of the contained materials. Batteries are complex products with a large variety of sizes and shapes which causes serious difficulties for predicting and carrying out its fragmentation.Domestic-type batteries are essentially of the Zn-Mn systems and with cylindrical shape, varying from the large size Mono (or D) type to the small size Micro (or AAA) type [1]. Recycling of batteries involves collection, sorting [2] and metallurgical processing [3, 4]. In some processes, the first step of metallurgical processing is dismantling and size reduction by shredding. Research work on spent batteries considering grinding/shredding and physical separation of fractions is scarce [5-7], but investigation in this domain is very necessary."

Jan 1, 2008

By Fuqiang Zheng, Feng Chen, Wenting Duan, Yufeng Guo, Tao Jiang

High-quality titanium-rich material is of significance in the development of titanium industry as it is the main raw material to produce sponge titanium and titanium white using chloride process. Activation roasting of titanium slag with high Ca and Mg contents as adding H3PO4 followed by acid leaching was investigated to prepare titanium-rich material. The effects of H3PO4 dosage, roasting temperature and time, hydrochloric acid quantity, acid leaching temperature and time on TiO2 grade and removal of impurities were studied. The results show that after the finely ground titanium slag roasted with 8% H3PO4 at 1000 for 2h, most Mg impurities in anosovite solid solution structure were converted into simple acid–soluble compounds. The impurities such as Ca and Mg obviously decreased when the hydrochloric acid concentration was 20%, leaching at 100 °C for 2h, from which a titanium-rich material containing 82.56% TiO2 and 1.15% (CaO+MgO) was obtained.

Jan 1, 2016

By Z. Smieszek, Z. Szota, P. Gajowski

"A new method for measuring the total quantity of suspensions contained in the electrolyte during copper electrorefining has been developed by the Institute of Non-Ferrous Metals, Gliwice. Electrolyte purity, and the suspensions content in particular, is of essential importance for the quality of electrolytic copper produced during the process. Suspensions contribute to the increase of slime impurities in electrolytic copper and increase losses in noble metals. Up to now, the laboratory method has been used for the· process control which provides analytical results with considerable time delay. Therefore, it is useless for the process control.The measuring method developed enables continuous measurements of a suspensions content directly within the stream of the flowing electrolyte. The principle of measurement is based on changes in optic properties of the electrolyte with varying suspensions content.1. IntroductionIn copper electrorefining, it is essential that the final product quality be maintained. If suspensions are present in electrolyte, the content of slime impurities in electrolytic copper, (such as Pb, Ag, Bi, Sn, Sb, and As), increases which can result in the occurrence of the so-called slime dendrites on cathodes, thus debasing the quality of the product. As a normal suspension content in electrolyte, the contents in the order of several mg/l are considered, usually not more than 5-6 mg/l, while contents exceeding 20 mg/l are referred to as an alarm state. Suspensions present in an electrolyte are usually a light fraction of anodic slime whose main components are metallic silver, lead sulphate, complexes of antimony and arsenic, and sometimes even calcium sulphate; they are mainly composed of very small particles of lead sulphate and antimony complexes. Sometimes - - in case of alarm states - - the so-called ""wandering slims"" can be observed, which are composed mainly of arsenic and antimony complexes. These ""wandering slims"" make a serious technological disturbance. In normal operating conditions of the electrorefining plant, an increase of suspension content can result from such reasons as crack of filter cloth in a slime filter, turbulent flow of the electrolyte, anodic passivation, aeration of the electrolyte, and improper servicing of an electrolytic tank. It is necessary to continuously control the suspensions content in electrolyte for proper electrorefining."

Jan 1, 1989

By R. A. Sharma

Neodymium metal was successfully produced by the reduction of Nd203 with Na in the presence of CaC12-NaCl melts by the overall reduction reaction Nd203 + 3 CaC12 + 6 Na ? 2 Nd + 3 CaO + 6 NaCl at -750°C. The metal produced was extracted from the salt media by dissolving it in a Nd-Fe alloy pool. The yield (percentage of theoretical neodymium produced) was found to depend on the salt composition and the mass ratio of salt to neodymium in the reactor. A yield of 95% was obtained with salt ratios as low as 3.5. Further decrease in the salt ratio below 3.25 decreased the yield. Stirrer position had little effect on yield; while increasing the temperature and placing fins in the reactor increased the yield. The Nd-Fe alloy produced was of as good quality as that produced using Ca reductant, and was suitable for direct use in producing General Motors MAGNEQUENCH? alloy for permanent magnets.

Jan 1, 1989

By Wantae Kim, Jaechun Lee, Tatsuya Oki, Sungbaek Cho, Sangbae Kim

"Effect of attrition scrubbing on the recovery of platinum group metals(PGMs) from automotive catalytic converter was discussed. The attrition scrubbing as comminution and separation process was effective for the recovery of the catalyst layer, ?-alumina, from ceramic supporting matrix, cordierite, by physical impact and shearing action between particles in the scrubbing vessel. The catalyst layer was dislodged from the surface of the supporting matrix into fine particles less than 45µm by attrition scrubbing. The production of fine fraction less than 45µm increased as the residence time for attrition scrubbing increased. The fine fraction obtained at the residence time of 40min contained 19.25% CeO2, 1.93% ZrO2 and 418.8ppp PGMs. The recovery of ?-alumina in the fine fraction increased as the residence time increased. Simultaneously, the recoveries of CeO2, ZrO2 and PGMs increased and reached up to 82.9% CeO2, 78.7% ZrO2 and 78.9% PGMs at the attrition scrubbing time of 40min. The production of the fine fraction and recovery of ?- alumina increased when the solid concentration and initial feed size increased.IntroductionThe automobile catalytic converters contain appreciable amount of PGMs. Currently several million tons of used catalytic converters are disposed annually worldwide, each containing about 0.5-1g of platinum and 1-2g of all PGMs1). The recovery technologies of PGMs from spent catalytic converters have been thoroughly reviewed by numerous researchers since last decades. Two types of methods, wet and dry processes, have been commercially operated. In the wet process, the PGMs on the spent catalytic converters were dissolved mostly in the form of chlorocomplex, MCl6 2-, by contacting with aqueous solutions. Subsequently the resulting solutions are treated to concentrate and the precious metal ions are reduced by introducing metals such as Al, Fe and Zn in the concentrated system2). In the dry process, the spent catalytic converters are melted, in some case with CaO, at an elevated temperature to produce a low viscous slag. The PGMs in the melt are separated by allowing them to adsorb on Fe or Cu having high specific gravity7). Although highly pure precious metals could be obtainable, the recovery technologies of PGMs currently operated seem not to be cost-effective since PGMs embedded in these types of catalytic converters are present in very small quantities."

Jan 1, 2008

By Youn-Bae Kang, Jong-Jin Pak, Min-Kyu Paek

The critical evaluation and thermodynamic optimization of Mn-Si-C and its sub-binary systems have been carried out over the whole composition range from room temperature to above the liquidus temperature. The solution properties of the liquid systems have not been clearly described because the liquid solution exhibits a high degree of short-range-ordering. In order to predict the thermodynamics of the liquid solution, the liquid phases were optimized by the modified quasichemical model. The model parameters of the solid phases were also optimized by the compound energy formalism to best reproduce the phase diagram and important thermodynamic properties in Mn-Si-C system. Using the model parameters, various thermodynamic calculations were carried out. The present database will be a part of larger thermodynamic database for the ferromanganese alloy database.

Jan 1, 2014

By C. M. Wai

"Metal species in solid and liquid materials can be extracted by supercritical carbon dioxide containing a suitable ligand. This in situ che1ation-supercritical fluid extraction technique offers several advantages over conventional solvent extraction including minimization of organic liquid waste generation and exposure of personnel to organic vapors. One unique feature of this technique is that metal species can be removed from solid materials directly using supercritical carbon dioxide as a solvent. Several ligand systems including dithiocarbamates, B-diketones, organophosphorus reagents, and macrocyclic compounds have been tested for metal extraction in supercritical carbon dioxide. This novel extraction technique may have important applications for metal recovery and mineral processing.IntroductionSupercritical fluid extraction (SFE) offers several advantages over conventional solvent extraction including the minimization of organic liquid waste generation and exposure of personnel to organic vapors.[1] The high diffusivity, low viscosity, and T-P dependence of solvent strength are some attractive properties which make supercritical fluids excellent candidates for extraction and recovery of organic compounds from solid materials [2] Carbon dioxide is a gas of choice for SFE because of its moderate critical constants (Tc = 31 °·C and Pc = 73 atm), inertness, and availability in purified form. After extraction, the fluid phase is depressurized to separate organic solutes from CO2 gas and the gas can be recycled for repeated use. The SFE technology has been applied to industrial scale operations such as the preparation of decaffeinated coffee and hop extracts."

Jan 1, 1996

By Baptiste Laubie

Agromining is a phytotechnology aiming at producing commercial metal compounds from low-grade ores thanks to hyperaccumulating plants. The fern Dichranopteris dichotoma is a rare earth element (REE) hyperaccumulator, which naturally grows on former mine tailings in China. It accumulates up to 0.35% of REEs in its aerial parts. Different hydrometallurgical processes are currently developed to recover these elements directly from the biomass or from ashes after combustion. The process presented here consists of a direct extraction by EDTA solution, followed by precipitation with acid oxalic. Optimal precipitation pH and influence of organic matter are determined by modelling and by experimental studies. The final solid contains 4.3% of REEs, with calcium as the main cationic impurity (0.45% of the precipitate). The recovery yield is similar for major REEs and is around 70%. After optimization, upscaling of the process will allow the agromining development to recover REEs from secondary resources with more environmentally friendly techniques.

By Shinroku Matsuzaki

Data the measurement sensor installed with spatial distribution on the blast furnace were successively accumulated online from the process computer to the database system over a long period. This is a new system that accurately considers the relation with the installation position of each sensor, and picture computerization of the measurement data was developed. The overall operation state of a blast furnace, which skilled operators can see in their mind?s eye, was objectively visualized as pictorial information.

Jan 1, 2006

By Lifeng Zhang, Zineb Benouahmane, Yaqiong Li

Experimental oxidation tests at high temperature (1000-1200 °C) on SiC samples have been respectively performed under wet and dry air atmosphere for different holding times. The thickness of thermally grown oxide was experimentally measured by DEKTAK Stylus Profilometry. The results showed that the oxidation rate was increased with temperature and holding time, corresponding to a passive oxidation regime which led to the formation of SiO2 layer. The sessile drop method was employed in order to measure the contact angles between Si and SiC at high temperature. Contact angle can be varied from 39.6° to 75.6° by controlling the atmosphere. The deoxidation of the oxide layer and infiltration of liquid silicon caused a decrease in the contact angle.

Jan 1, 2016

By Jae-Chun Lee, Jinki Jeong, Manis Kumar Jha, Divika Gupta, Pankaj Kumar Choubey

Rare metal indium (In) is mostly used as electroluminescent material in liquid crystal displays (LCD) monitors. Present paper describes leaching studies for the recovery of In from waste LCD monitors in presence of different other impurities. The leaching studies showed that more than 85% of In was leached out using 20% sulfuric acid at 60oC in mixing time 30 min at fixed pulp density 25 g/L. The solution could be purified using SX/IX and from the pure solution metal/ salt could be produced by evaporation, precipitation, electrolysis, crystallization processes.

Jan 1, 2014

By Ragnhild Aune

In fire refining of copper, the affinities of various impurity elements on dissolved oxygen is of great significance. Further, in the design of oxygen probes in liquid copper, the influence of solute interactions on the activity of oxygen need to be considered in order to evaluate the oxygen concentration in molten copper. The present paper presents a series of measurements of the activities of oxygen in liquid Cu-M-o alloys (where M stands for Mn, Zn, As, Se or Te) carried out by the present group employing the solid electrolyte galvanic cell technique. Extreme care was taken to control the oxygen potentials in the inert gas atmosphere, and to keep the oxygen levels very low in the molten metal. The oxygen content was determined by analysis of the samples taken out from the melt. The results obtained showed that Mn has a strong negative influence on the activity coefficient of oxygen in liquid copper. A similar, but less prominent effect was observed in the case of Zn. Arsenic had no influence on the activity of oxygen in Cu (liq.). Se and Te had slight negative effect on oxygen activities in copper at XO > 10-5, while at lower oxygen levels the interaction coefficients were found to be positive. The results obtained were compared with empirical models for the calculation of interaction coefficients available in literature.

Jan 1, 2003

By S. J. Buckler

Many chemical and metallurgical processes use submerged gas injection to increase contact area between gas and liquid phases in order to promote faster overall reaction or refining rates. The total interfacial area produced by gas injection through lances, nozzles or tuyeres is both an important design parameter for new vessels and a measurement for estimating the maximum processing capacity of existing equipment. Estimating total interfacial area from submerged injection into industrial pyrometallurgical vessels from existing knowledge is a problem with two aspects. The first difficulty is the difference in behaviour of cold (aqueous) and hot (molten metal) systems, implying that existing models and correlations of gas-liquid behaviour developed in low temperature systems are not necessarily appropriate for estimation of high temperature behaviour. The second difficulty is the issue of scale-up of correlations from laboratory to industrial sized vessels. The work presented in this paper is part of an ongoing experimental investigation, at the GK Williams CRC for Extractive Metallurgy, to quantify the total gas-liquid interfacial area available in pyrometallurgical vessels using chemical measurement methods. The effects of three operating variables, injected gas flow rate, nozzle diameter and nozzle submergence, on total interfacial area are quantified in a IOOL aqueous system - the first stage of a three stage process in examining the implications for scale-up of high temperature, medium-scale results are discussed. The results of work at high, injected gas flow rates (up to 500/min) show that the submerged Froude number is not sufficient for use as the sole variable in a predictive model of total interfacial area. Further work is being undertaken to identify other dimensionless variables that will better represent the gas-liquid characteristics in submerged injection that influence the formation of total interfacial area. The second and third stages of the experimental investigation involve measuring the total interfacial area in a large-scale (1000L) aqueous sodium sulphite and small-medium scale molten metal baths.

Jan 1, 2002

By G. L. Peralta

Geothermal energy is an important source of power in more than 12 countries and is a potential source in 50 countries. However, the exploration and use of geothermal resources generate residues such as scale and sludge. The scale is from the steam distribution pipes while the sludge is from cooling ponds. These solids contain significant levels of elements which are of environmental importance notably, arsenic, sulfur, copper, zinc and lead that require safe treatment and disposal. The compositions, phases, textures, morphologies and size of scale and sludge particles have been studied by laser particle size analysis, light microscopy, scanning electron microscopy, X-ray microanalysis, and X-ray diffraction. In addition, their leachability was tested with protocol leaching procedures and sequential extractions. The detailed spatial relationships and speciation of the environmentally significant constituents have received particular emphasis. The information obtained is useful in understanding how the scale and sludge are formed, their leaching behavior if disposed of in a landfill and in developing appropriate treatment strategies.

Jan 1, 1994

By Tom Marttila

During the last few years, when a new tankhouse or a major modernization has been planned, automatic or semiautomatic crane and grab systems have at least been considered. It seems that in the future tankhouse managers for new, modernized and even old tankhouses will be looking for a proven and reliable system for automatically moving and positioning electrode loads in the tankhouse and in storage areas. In this paper, we will describe the Wenmec solution for automatic electrode handling. The advantages of automatic handling and very accurate electrode positioning will be discussed, and the way Wenmec has solved the problems in mechanical construction and in automatic, accurate and reliable positioning will be presented.

Jan 1, 1990

By Takamitsu Nakasuga, Haiping Sun, Kyushu University, Katsumi Mori

"The kinetic behavior of reduction of chromite ore by liquid iron containing carbon and silicon has been investigated under various experimental conditions to clarify the reduction mechanism. It was found that the reduction rate of chromium ore by liquid Fe-C alloy was very slow. In addition, when carbon and silicon coexisted in the iron melt, silicon was found to preferentially oxidized to form silica, which favored for the fonnation of liquid slag and the rate of reduction was considerably accelerated. The similar effect was obtained by the addition of some fluxes, such as SiO2, Na2B407, CaO-SiO2, which also promoted the formation of a liquid slag and thus the reduction rate in the early stage also increased.IntroductionThe reduction of Cr2O3 is a basic reaction for production of ferro-chromium from chromite ore and for chromium recovery from the slag fonned during the decarburization period of a stainless steel-making process. The reduction of chromite ore consumes much energy and its reaction rate is not so high. Thus, in order to increase the reduction efficiency, it is strongly desired to clarify its reduction mechanism from the practical and the theoretical points of view."

Jan 1, 2000

By R. P. King

The linear intercept distributions provide unambiguous and accurate characterizations of the texture of mineralogical materials. The relation between the measured linear intercept distributions and the spatial correlation function is shown to be given by: in the Laplace Transform domain. The linear intercept distributions of the two phases in a low- grade chromite-serpentinite ore were measured. and the spatial correlation functions for both phases were evaluated using the above relation. The correlation functions are the primary relations for integral geometric models of mineralogical texture and this work demonstrates the relation between the 10 stereological model and the 3D integral geometry model for mineral liberation.

Jan 1, 1991