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By J. A. Innes

"""The oxygen, next uniting with the carbon, sent up an ever-increasing stream of sparks and a voluminous white flame. Then followed a succession of mild explosions, throwing molten slags and splashes of metal high up into the air, the apparatus becoming a veritable volcano in a state of active eruption.""IntroductionHenry Bessemer F.R.S(An autobiography, 1905)Thank you Mr Chairman for the opportunity to speak: at this, the opening session of your International Symposium on the subject of ""Injection in Pyrometallurgy"". Judging from the list of papers to be presented over the next three days, the Symposium promises to provide a most valuable addition to our existing knowledge base in what is now an extremely active area of R&D investigations. Whilst we have obviously come a long way since Sir Henry Bessemer's pioneering experiments of the mid-19th century, there is still much for us to learn.Most importantly, the Symposium offers a further opportunity to acknowledge the many significant technical contributions made in this field by the Organising Committee's special guest, Professor Howard Worner - one of this country's most respected research leaders.When first approached to give this talk I had two areas of concern. Firstly, I was not entirely clear just what injection metallurgy was meant to cover. How should the overall scope of this particular subject be defined?My second concern related to Howard Worner himself - a man for whom I have the highest personal regard and who, in fact, played a most influential role in respect of shaping my own career. Having already spoken about Howard's achievements on earlier occasions, I wondered what I could sensibly add.Notwithstanding these personal reservations, I am delighted to be here with you this morning. If my thoughts on the meaning and scope of injection metallurgy appear to be slightly off-course, and if Howard should perhaps recognise some repetition in my remarks, then I hope I can be forgiven."

Jan 1, 1996

By Wolfgang Baum

Case studies from epithermal gold-silver deposits in the western United States and in Latin America show that the routine use of process-related mineralogical studies has become an important tool for the reduction of development, capital and operating costs. Bypassing the mineralogical characteristics of epithermal gold-silver ores, as a result of fast-track development approaches, has resulted in multimillion dollar metal losses and/or in considerable modification costs of existing operations.

Jan 1, 1988

By D. W. Ashman

The zinc pressure leaching plant at Cominco's Trail Operations is now in its ninth year of production. The plant produces a zinc sulphate and jarosite slurry which is further processed in the calcine leaching circuit. Elemental sulphur, a by-product of the process, is sold in the North American market. During the past eight years, a number of changes have been made to the plant to remove known production bottlenecks and to improve leaching extraction. These changes have raised production rates above the initial design so that the plant currently accounts for approximately 20 percent of Trail s zinc production. These rates are expected to be increased further upon the completion of the alterations currently in progress. The knowledge gained over the operating life of this plant has allowed Cominco to plan for a possible future expansion of the zinc pressure leaching plant. If expanded, zinc pressure leaching would account for approximately 48 percent of cominco?s zinc production.

Jan 1, 1990

By Yonggang Liu

Microstructure and precipitates in hot rolled low carbon steel sheet by CSP were investigated in this paper. It is pointed out the precipitates in low carbon steel sheet by CSP are different with that by traditional hot rolling. The bainites were found in CSP hot rolled steel sheet by TEM testing and these bainites could maintain in the sheets even after batch annealing. The selected area electron diffraction analyzing indicated that there were many CrB2BN and FeB4BN phases precipitated in hot rolled steel sheet and no AlN grains precipitated. The nitrides forming can limit AlN grains precipitating during the batch annealing processing, and this could do harm to the texture pipeline along orientation line forming with formed properties.

Jan 1, 2006

By Kurt A. M. Westerlund

The basic function of primary gas handling downstream non-ferrous pyro-metallurgical processes is cooling hot sticky gases to treatable temperature levels (e.g. entering ESP). That means managing efficient the critical gaseous components from a molten via a sticky to a solid phase. The article outlines the modem gas cooling methods combined with efficient heat recovery. Examples of the alternative use of recovered steam energy are outlined; as e.g. drying of concentrate and power generation. The heat transfer impact of the insulating dust is called fouling and circumstances causing fouling are described. Modem cooling surface design and cleaning techniques to keep fouling in reasonable limits are described. Leakage- and false air ingress into the gas handling lines often limits smelting capacity. The objective is generally to minimize the infiltration of air but it still takes place at open interfaces (e.g. at reactor hood, feed port). Leakage air at furnace roofs for example can be reduced to a minimum by adopting the pressure gas sealing used at present In-Bath-Lance furnaces. Modernization and optimization methods to de-bottleneck existing waste heat boiler gas cooling capacity by highly efficient surface cleaning systems and false air avoiding (e.g. bundle roof boxes, dust discharge) are detailed described.

Jan 1, 1999

By K. Lillkung, O. Forsen, J. Aromaa

"The dissolution rates of Pt, Pd and Rh in 250 g/L NaCl solution were calculated from the current densities determined by polarization curves and potentiostatic measurements measured with wire electrodes at atmospheric pressure. The results achieved with the two methods were similar. The dissolution rates at the corrosion potential were in the order of few nanometers per hour. The polarization curves indicated that to achieve dissolution rates required for economical operation on an industrial scale, the samples need to be polarized to higher potentials. When polarized to higher potentials, the metal dissolution rates were in the order of micrometers per hour. As the Tafel slopes of the metal dissolution region are fairly steep, the potential affects the dissolution rate greatly. Based on the activation energies, the dissolution reactions were controlled by a charge transfer step.IntroductionPlatinum group metals (PGM) have some very unique properties such as their inertness, giving excellent corrosion resistance, and a high melting point. At the same time, these factors make the refining of these metals very challenging. The main applications where PGMs are used are different catalytic converters, mostly in automotive catalysts. The used catalysts are also an attractive secondary source of PGMs. The exact concentrations of PGMs in catalysts vary widely depending on the manufacturer, the age and the capacity of the catalyst. The concentration of Pt in a new catalytic converter range from 300 to 1000 ìg/g, Pd from 200 to 800 ìg/g and Rh from 50 to 100 ìg/g [1]. Precious metal catalysts usually consist of a coat of the metal supported on ã- alumina. The recovery of metals from automotive catalysts has received much attention during the last few years [1-3]. In the near future, the use of PGMs in fuel cells is predicted to increase the amount of secondary PGMs available [4]."

Jan 1, 2012

By G. T. Lapidus, O. J. Solis-Marcial

"The oxidative dissolution of copper from refractory minerals, such as chalcopynte, represents a technological challenge that has occupied hydrometallurgists for more than half a century. Innumerable processes have been suggested, but the majority operates at high temperatures or employs corrosive media. The origin of this refractory nature is the formation of passivating phases of iron(III) or copper. One option is to add non-corrosive ligands that complex these metal ions, thereby facilitating their dissolution. In the present work, the effect of acetone in sulfuric acid solutions was studied. The initial experiments were on chalcopynte carbon paste electrodes using cyclic voltammetry, where greater reactivity was observed. Later, leaching tests with hydrogen peroxide, cupric sulfate and ozone and, as oxidants, were performed. High extractions were achieved in three hours at 50°C. The solid residues contained the iron in the form of Fe203 and FeOOH.IntroductionChalcopyrite is the most important mineral of polysulfide copper ores [1] and accounts for approximately 70% of the world's copper reserves [2]. Currently, the copper present in chalcopyrite is extracted mainly by pyrometallurgical processes, which generate environmental concerns because of the formation of SO2 gas and submicron particulates [3]. The development of a less aggressive hydrometallurgical process for the extraction of copper would constitute a possible solution to these problems. For that reason, studies of the dissolution behavior of chalcopyrite are of great technological importance [4], However, the proposed oxidative leaching routes for chalcopyrite, generally at high pressures and temperatures, have not been implemented on an industrial scale, because of the elevated costs required to equal the high copper extractions obtained in thermal processes. These extreme leaching conditions are required because of the refractory nature of chalcopyrite. Passivation has been used to explain this phenomenon, although researchers have disagreed on the composition of the layer, which is various have assumed to be sulfur, copper sulfides, and iron-bearing jarosites or hydroxides [5]. If the latter compounds are the cause, an alternative solution would be the use of polar organic solvents in the oxidative leach to decrease the formation of the passivating iron layer. In this work, the influence of acetone on the oxidative leaching of a chalcopyrite concentrate at room conditions is explored."

Jan 1, 2012

By Xiping Chen, Wangxing Li

"Spent potlining is unavoidable solid waste from aluminum smelters. About thirty kilograms spent potlining is discharged in China to produce per ton primary aluminum. Spent potlining has high level soluble fluorides and cyanides so that it brings heavy pollution to environment. It is prohibited to keep a large amount of spent potlining in open air because it will lead concentrated pollution to local soil and water source due to hydrated reactions between spent potlining and rain water/moisture in air. Landfill may solve pollution of spent potlining provisionally, but it is difficult to be accepted by aluminum smelters because of its high investment, troublesome monitoring and perennial maintenance. Detoxifying of spent potlining not only can remove deleterious fluorides and cyanides in SPL, but also can make fluorides in SPL recycle and return to aluminum electrolysis cells, at the same time benign SPL solid residue can be recycled and ready for cement production.IntroductionChina became the largest primary aluminum manufacturer in 2001. In the past few years, its aluminum output increased by twentyfive percent every year and reached 12.56 million metric tons in 2007. The whole world was very surprised and focused attention upon Chinese aluminum industry. It is more and more important to keep sustainable and steady development with the rapid development of Chinese economy. Aluminum industry is an important base industry and does a great contribution to Chinese economy. But aluminum industry is high energy-consumption and heavy-pollution industry. The government has paid more attention to aluminum industry in recent years. Nowadays the bothersome problem which counterworks Chinese aluminum industry is pollution from solid wastes. Main Solid wastes from aluminum industry are red mud from alumina refineries and spent potlining (short as SPL) from aluminum smelters. Spent potlining are waste lining materials from aluminum electrolysis cells. During production of aluminum, due to reactions between melted electrolyzer and pot lining as well as penetrating of fluorides into pot lining, newly-formed compounds inlayed in pot lining, destroyed the lining structure and brought pot lining cracking. Melt rushed out of lining cracks, cells have to be stopped running and ready for heavy repair. Cell life generally varies from 1500 to 2000 days. Spent potling is an unavoidable solid waste from aluminum industry."

Jan 1, 2008

By Ulrich Kerney

In 1996, bath smelting technology for lead recovery from concentrates and secondary materials was introduced in Nordenham to replace the common sinter plant/shaft furnace operation. Since start-up, a continuous improvement of equipment and operation lead to a steady increase of capacity and plant availability. The decision to skip the reduction stage for slag treatment now allows the treatment of 200000 t/a feed materials with a secondary fraction of up to 70 %. The main feed source for the furnace is automotive battery recycling, which offers oxide paste and metallics to be molten under oxidizing conditions in the lance fired furnace. The lead bullion is transferred to the refinery, where copper, silver and other impurities are removed. Silver is recovered as doré quality. All loopings are recycled to the BSF. Inert feed material is collected in a so-called lead concentrate of metallurgical origin, the primary slag, which is sold. It is rather a valuable feed material for further processing than a slag The off-gas is cooled in a flux-flow system, entering then an electrostatic dust precipitator. Having passed a further washing and cooling system, SO2 is oxidized and collected and sold as concentrated sulphuric acid. The presentation will cover a review of the start-up phase, the development of significant production parameters over the last years and actual production routes and figures. A comparison of environmental data between new and old applied technology is made.

Jan 1, 2006

By Bo Jiang, Lianyun Liu, Hongmin Zhu, Kai Huang

"Watermelon peel is selected as a novel adsorbent to remove Pb(II) from aqueous solution. A simple saponification process is proposed to modify the peel and the adsorbent is characterized by SEM and FTIR. The effects of pH, contact time, initial concentration of Pb(ll), biosorbent dosage and temperature on adsorption of Pb(II) are investigated. Different models are used to fit experimental data. These models indicate that the adsorption process follows the Langmuir model and pseudo-second-order model. The maximum adsorption capacity obtained from Langmuir model is 1.05mol kg-1 for the prepared sorbent. Equilibrium time is attained in 5-10 min for the studied concentrations. The watermelon peel can be used as an effective and low-cost biosorbent for removal of Pb(ll) from aqueous solution.IntroductionRecently, removal of heavy metal ions from industrial effluents by biosorption has become a very attractive topic, since the more serious pollution issues caused by heavy metals emerge frequently, and more strict requirements for its control are called upon by society [1,2]. In this case, most conventional purification technologies are not suitable due to poor cost-effectiveness [3]. For example, chemical precipitation by alkaline reagents usually can not decrease the metal ion concentration below the permissive levels, and also it will produce a large amount of sludge containing toxic metals. Membrane separation techniques can realize deep purification of wastewater easily, although its operating cost is usually high. Thus, considering the high effectiveness, low cost and free-sludge operation, bisorption has become a promising technique in water treatment [4]. The most important thing for this technology is the synthesis of a suitable biosorbent, whose adsorption properties will determine the removal efficiency and economic cost for the whole process. Watermelon is one of the most popular fruits for mankind for its delicious flavor. Usually, the watermelon is consumed mainly for its edible pulp, and its peel is discarded or only used as feed for livestock. Considering the pectin contained in the watermelon peel, just like that in orange wastes in the reported literatures [3], the idea of using it as the raw material to prepare the biosorbents for heavy metal ions removal from the aqueous solution was evaluated in this study."

Jan 1, 2012

By Daniel A. Norrgran

Grinding ball fragments discharging from SAG mills and ball mills causes extreme wear to downstream processing equipment. These ball fragments, recirculating in a milling circuit, will cause excessive wear to sumps, pumps, hydrocyclones, and interconnecting piping. A magnetic separation system to remove grinding ball fragments from the mill discharge has been developed and successfully applied in the milling circuit. This magnetic separation system - termed Trammel Magnet - was first applied at the Escondida copper concentrator in Chile. The Trommel Magnet consists of an arc of permanent magnets mounted at the discharge end' of the tommel screen. The magnetic arc attracts the ball fragments and removes them from the process stream. This retrofitted magnetic separation system removed 126 metric tons of ball fragments from the circulating load of a. single ball mill in the initial 24 hour period. The mill has since stabilized and the magnetic separator is currently removing 7 metric tons per day of ball fragments. The retrofit of the Trommel Magnet has: 1. Extended the pumpp life and the hydrocyclone life approximately 300 percent. 2. Provided a 5 percent increase in the throughput of the mills by removing grinding ball fragments that contribute very little to the grinding process. Variations of the Trommel Magnet have also been developed for removing grinding ball fragments directly from the mill discharge without the use of a trommel screen. In each case, permanent magnets are used to collect the ball fragments from the mill discharge stream prior to reporting to the sump. These other systems have been designed and fabricated for in-plant test work.

Jan 1, 1999

By Brian G. Thomas, Quan Yuan, Rajneesh Chaudhary, Rui Liu, Sana Mahmood

"A particle-entrapment model based on local force balances has been developed, implemented into computational models of turbulent fluid flow, and applied to simulate the entrapment of slag inclusions and bubbles during the continuous casting of steel slabs. Turbulent flow of molten steel is computed in the nozzle and mold using transient CFD models. Next, the transport and capture of over 30,000 particles are simulated using a Lagrangian approach. Particles touching the dendritic interface may be pushed away, dragged away by the transverse flow, or captured into the solidifying shell according to the results of a local balance of ten different forces. This criterion was validated by reproducing experimental results in two different systems. Finally, the model is applied to predict the entrapment distributions of different sized particles in a typical slab caster. Although more large particles are safely removed than small ones, the capture rate as defects is still high.IntroductionSurface defects such as slivers and blisters are often caused by captured inclusion clusters, slag, bubbles, and other particles. During continuous casting, jets of molten steel from the submerged entry nozzle (SEN) ports carry bubbles and inclusion particles into the mold cavity from upstream processing, as shown in Figure 1 [1]. In addition, droplets of liquid mold slag may become entrained into the flowing steel due to fluid flow problems, via several different mechanisms [2]. Figure 2 shows some typical inclusion particles [3] that can be entrapped from the flowing liquid into the solidifying steel shell to form defects in continuous-cast product.Liquid steel flow in the continuous casting mold has been modeled extensively. Reynolds Average Navier-Stokes (RANS and URANS) approaches are based on accurate computation of the ensemble-averaged velocity field. Particle transport can be tracked using a Lagrangian approach, introducing an extra model, such as ""random walk"" to generate realistic motion of every particle. Large Eddy Simulation (LES) models can accurately calculate both the transient evolving flow field and Lagrangian particle motion [4, 5] of this turbulent process."

Jan 1, 2012

By Aurelian Buzaianu, Cristian-Aurelian Popescu, Gabriela Popescu, Petru Moldovan

"A lot of scraps result in processing of composite materials which contain metallic phases that can be recovered and used again in different field. Considering this point of view the aim of the paper was to separate and recover aluminum from aluminum matrix/graphite composites. The separation and recovery of aluminum alloy from aluminum alloy/graphite composites was done by treatment with halide molten salts. As halide salts were used flux tablets that collect the ceramic particles in dross. After dross separation, was used filtration in order to separate the aluminum matrix from the other impurities.Samples from the recovered alloy were analyzed using chemical analysis, optical and electron microscopy, as well as X-ray diffraction. The desired composition of the aluminum alloy obtained from scraps could be reached by some addition of metals to the metallic phase. From optical microscopy it was obvious that the structure of the aluminum alloy obtained after composite reclamation consists large particle of silicon, eutectic, a-Al solid solution and other phases like Fe, Si, Mg and Ni, or some compounds like CuAl2. 1. IntroductionThe research on the recycling and reclamation of metal-matrix composites (MMCs) becomes active to preserve the natural environment, as environmental requirements become stricter, to save energy, and to reduce garbage. In case of recycled aluminum alloy ingot the production energy is about 3 pct of that of the new ingot. This evidence strongly supports the necessity to recycling of aluminum alloys. Among aluminum alloys, metal matrix composites have high strength and elastic modulus, and also good were resistance. These materials have been developed to meet the demand properties which exceeds that of the ordinary materials, and to save energy."

Jan 1, 2008

By Hélio Wiebeck, Fabio J. Esper, Wildor T. Hennies, Guillermo R. Martín-Cortés, Francisco R. Valenzuela-Díaz

"Natural rubber reinforced commonly with carbon black to produce vulcanized material, turns into a new environmentally friendly nanocomposite when carbon black is replaced by organically modified clays of Brazil. Carbon black is substance derived from the oil refining process with consequent pollution to the environment. Its substitution in this industrial process must contribute to diminish the oil derived products dependence. As the added clays are only a third in weight of the traditionally carbon black added, then, to obtain the same final volume it is necessary to add low cost neutral filler that does not damage the technological characteristics of the final material. This paper presents results using as neutral filler of this type rice husk ashes from industrial wastes. Experiences realized with this nanocomposite material show results of quality and technological characteristics similar or superior to those of the rubber made with carbon black.IntroductionTraditionally rubbers are black or a very dark color. But they can have different appearance when filler of distinct composition of the carbon black is used. The carbon black is substance derived from the oil gotten during the final phases of the mineral fuel treatment with consequent pollution of the environment. Carbon black show nanometric grain sized distribution and a depth black color, because these properties it is also used for computer printers inks production. The substitution of this substance, traditionally used as a reinforced load in the rubber production, will have to contribute in such a way to diminish the dependence of these products as to diminish the pollution of the environment. The present work shows the results of the use of another kind of mineral nanoparticulate material substituting carbon black in the production of some rubber products. This nanoparticulate material is the organic modification of smectite clay treated with some types of ammonium quaternary."

Jan 1, 2008

By John Petersen

Heap bioleaching technology has become well established for the exploitation of copper sulfide ores. Still, in many operations the rate of copper extraction is rather slow, often taking two years or more to recover 80% of the copper. Chalcocite, the most common secondary copper sulfide, leaches by a two-stage mechanism. The first stage is rapid, whereas the second stage has a high activation energy and proceeds slowly at ambient temperatures. Nonetheless, this rate is still considerably faster than what is typically realized in a full-scale heap. A comprehensive column bioleaching study of a chalcocite ore has shown that the chalcocite columns are leached in a zone-wise fashion. The first zone corresponds to the first stage of chalcocite leaching, where all ferric produced by the bacteria is immediately consumed and all acid entering with the feed solution is consumed within a relatively narrow band. The second stage of chalcocite leaching proceeds much more slowly in the wake of the first stage, within a zone that grows gradually over the entire length of the column. The overall rate of leaching is thus determined by the rate of acid supply into the column rather than by mineral or bacterial kinetics, at least until the entire column is engaged in second-stage chalcocite leaching. In full scale heaps, there is evidence to suggest that solution distribution favours channelling between relatively large clusters of material which are exposed only to stagnant solution. Reagents have to migrate into such clusters by diffusion, which retards the delivery of acid dramatically. Thus, we believe that the rate of chalcocite oxidation in heaps is governed by sideways diffusion rather than downward migration. Column experimental results have been reproduced with a comprehensive heap-modelling tool. The model predicts that by simply changing the length of the average diffusion channel from column conditions (a few cm) to heap conditions (tens of cm), extraction times can change from weeks to years under otherwise identical conditions.

Jan 1, 2003

By Ana E. Bohé, Georgina De Micco, Gastón G. Fouga

"In this work the reaction between several manganese oxides and chlorine is investigated in the range of temperatures between 650 and 950ºC. The reaction path for the chlorination of MnO is established, which involves recrystallization of high valence manganese oxides (Mn3O4 and Mn2O3) followed by its chlorination. For this reason, to understand the reaction of MnO, the chlorination of Mn3O4 and Mn2O3 has also been studied. The starting temperature for the reaction of these oxides is determined by non isothermal thermogravimetric measurements. The effect of temperature is analyzed, under our experimental conditions the rate of reaction is mass transfer controlled. The activation energy for the volatilization of manganese chloride is obtained which is in good agreement with volatilization enthalpy of MnCl2.IntroductionMany oxide ores which have manganese in their composition undergo chlorination processes during the extraction of refractory metals such as Ti, Hf and Nb. Although several works related with chlorination of manganese oxides were reported, there is no information about the kinetics or mechanism of the manganese oxide chlorination reactions. Okahara et al. studied the chlorination of manganese oxides and established that they react easily above 250ºC. Furthermore, they observed that chlorination of high order oxides is more difficult when there is not a reducing agent [1]. Ivashentsev studied the chlorination of manganese oxides using Cl2(g), CO(g) + Cl2(g) and COCl2(g). He established that the reaction of MnO started at 130ºC with formation of MnCl2(s), he also observed recrystallization of manganese sexquioxide [2]. Finally, the chlorination of manganese nodules from the ocean was studied by Murthy and Reddy [3] with the aim of obtaining valuable metals such as Mn, Co, Ni and Cu. They studied the influence of several parameters like temperature, carbon percentage, particle size and chlorine flow rate in the extraction process."

Jan 1, 2008

By Luciano B. Oliveira, Luis G. C. Marques, Sergio N. Monteiro, Marcos V. M. Fagundes

"Biodiesel production is normally associated with large plantations of oily vegetables such as soybean and colza, in large rural areas. However, in the municipal limits of the city of Rio de Janeiro, southeast of Brazil, biodiesel is being produced from wastes commonly generated by typical urban activities such as sewage sludge, discarded fat from meat markets and post-used cooking oils. In the present work, the experience of producing biodiesel from urban wastes in Rio de Janeiro is assessed. The type of precursor materials, equipments and logistics are presented. The environmental and economical advantages as well as the drawbacks are discussed.IntroductionThe interest for a liquid fuel that could substitute those obtained from petroleum started more than one hundred years ago when Rudolph Diesel tested his no-spark internal combustion engine, impelled by compression, with peanut oil. By that time, petroleum was beginning to be extracted in large scale and no one was concerned with the future environmental problems and its eventual depletion. In the last century, the successful association of petroleum based fuels with the automotive industry was an almost insurmountable obstacle to any attempt to use nonmineral oils [1]. In addition to the greater efficiency and, by then, lower price of the diesel from petroleum, the use of plain vegetable oils introduced undesirable carbon deposits and reduced the engine lifetime. Today, the situation is reverse. The continuous increase in the price of petroleum and, above all, its contribution to climate changes are strongly motivating the use of biofuels to replace those obtained from fossil fuels such as petroleum, natural gas and coal [2].In the case of the common petroleum derived diesel, many countries are now engaged in large scale substitution programs. The USA should produce more than 700 million litters of biodiesel, while the European Community is expected too produce around 6.5 billion litters in 2008. In Brazil, the federal biodiesel program imposed a minimum of 2% addition to the common diesel. This would demand a production of 800 million litters in 2008 [3]. The Brazilian biodiesel is made from a diversified source of vegetables mainly castor bean, African palm and soybean. The main producers are agrobusiness firms located in large rural areas of the Brazilian hinterland [4]."

Jan 1, 2008

By Jong-Jin Pak

The present work reports the commercialization of a recycling process of spent acid to recover molybdenum. The process consists of ammonia gas neutralization of spent acid containing molybdenum, crystallization and filtration of ammonium molybdate, roasting and hydrogen reduction of molybdic oxide to produce a commercial grade molybdenum metal powder. The mother liquor, highly nitrogeneous residual solution after the filtration of ammonium molybdate, can be utilized to produce chemical fertilizers.

Jan 1, 2006

By Anand Kumar, Pradeep kumar Jha, Suman Kant, Pradeep Kumar

"It has been a major challenge to reduce the intermixed grade formation during ladle change-over operation in continuous casting process of tundish steelmaking. The F-curve generated by step input of the tracer (new grade steel) tells about the intermixed grade amount for different grade specifications. Use of flow modifiers is beneficial in reducing the intermixed grade because of the change in slope (in different time zones) and position of the F-curve due to their placement at tundish bottom. Present study aims at investigating the role of dam placed before the outlet in a multi-strand tundish with reference to the slope behavior of F-curve in different time zones during the teeming operation plays an important role in determining the intermixed amount.Introduction In Continuous casting process, the old grade steel remaining in the tundish (reservoir between ladle and mould) from the old ladle gets mixed with new grade steel from new ladle and leads to intermixed grade which is considered to be of inferior quality. Although formation of intermixed grade is inevitable with the sequential method of casting, its amount can be controlled by changing the flow behavior of steel inside the steel. Intermixing in a slab caster tundish was simulated using 3-D numerical model based on k-å turbulence equation and compared their result with that of water model experiment Yeh and Hwang [1]. Huang and Thomas [2] reported that quantity of residual fluid in tundish affects the composition distribution in the transitional slab and thus the intermixed length. Huang and Thomas [3] developed three sub models to predict mixing in tundish, liquid core of strand and solidification. Thomas [4] developed a one dimensional model to simulate the final composition distributions in slab caster of continuous casting and investigated the effect of process variables on the intermixing. Alizadeh mehdi et al., [5] simulated of the intermixing phenomenon for slab casting for three different sub models. Goldschmidt et al. [6] developed a numerical model that predicted the location of the intermixed steel in a four line round caster. Lan and Khodadadi [7] studied for the transient fluid flow of liquid steel, heat transfer and solidification during the flying tundish change process. Cho and Kim [8] developed a mixing model to predict the outlet concentration of the tundish during grade transition. Most of the work reported in the literature has dealt with intermixing in slab caster tundish. Billet caster units are more often being used by steel industries due to growing demand of billets. The multiple outlets lead to varying degree of intermixing with time owing to their different distance (location) from the inlet. Use of flow modifier to minimize the intermixed amount, however has also not been discussed in detail so far. Further no work has been reported regarding effect of slope of F-curves obtained through different outlets on intermixing. Hence keeping these objectives in mind attempt has been made by authors to analyze the slope of Fcurves after dividing them into three different time zones and the effect of these time zones on intermixing."

Jan 1, 2012

By Tapio Ahokainen

Commercial modeling software and increasingly efficient computers enable today computational fluid dynamics (CFD) to be used as a tool for a more comprehensive understanding of the flash smelting and flash converting processes. CFD modeling can be used for design purposes in many technological areas, but some relevant physical and chemical phenomena are still missing in the commercial CFD solver packages. Therefore, Outokumpu has developed several subroutines for solvers to describe analytically the phenomena in the flash smelting environment. CFD sub-models of the copper concentrate and matte combustion, the particle-particle-wall interactions and for more accurate radiation properties of the gas-particle suspension are needed to ensure reliability of numerical simulations on the flash smelting and converting vessels. Several basic combustion phenomena can be modeled with a number of commercial solver packages, but own models for combustion must be included in the case of sulfides as the feed. Mathematical models for copper concentrate and solid matte combustion have been developed during the last decade. They calculate compositions of the particles and temperature, based on extensive experimental research work in laboratory scale furnaces with validated kinetic parameters and temperature measurements of reacting particles. Inside and near the concentrate burner, the standard particle tracking methods do not include the particle-particle interactions and the particle-wall interaction is too much simplified to describe properly the particle collisions with the distribution cone. Therefore, additional models for the particle-particle as well as particle-wall interactions have been written and implemented. For thermal radiation, models for the emissivity of a gas mixture and for calculating the particle absorption and scattering coefficients have been developed and tested. In addition, the advanced radiation model can be used i.e. in the enhanced simulation of off-gas cooling in the heat recovery boiler area of the flash smelter.

Jan 1, 2006