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By M. Kane, O&apos

Operators and designers require a comprehensive model to predict performance of heap leach piles and provide input of reliable and defensible data for economic modelling. A conceptual, theoretical, or numerical predictive model addressing the required metallurgical, geological, biological, and operational considerations should be developed within the framework of the hydraulic performance of the heap leach pile. It is generally agreed that segregation, compaction, and consolidation are physical aspects which significantly affect recovery and in general hydraulic performance. Hydraulic performance of heap leach piles can be described through the application of unsaturated zone hydrology. Unsaturated zone hydrology describes the flow and storage of moisture and oxygen in a porous medium under conditions where the pore water pressure is less than atmospheric. The porous material is "unsaturated" if an air phase, in addition to the water phase and solid material phase, is present. These conditions describe the operation of a copper heap leach pile. This paper will focus on developing an understanding of hydraulic performance in segregated heap leach material and demonstrating that unsaturated zone hydrology can be used as the framework to improve understanding and prediction of heap leach performance.

Jan 1, 1999

By Nan Zhang, Lei Zhang, Gai-feng Xue, Lina Wang, Pu Liu

"A novel ß-diketone modified silica gel was synthesized by a simple reaction. The prepared material was characterized by diffuse reflectance FTIR spectroscopy and it was used for the adsorption of heave metal ions in the industrial waste water. The main parameters affecting the sorption of heavy metal ions, including pH, water flow rate, and elution, have been investigated in detail. Under the optimized operating conditions, most of the targeted heavy metal ions could be removed. The material could be simply regenerated by hydrochloric acid solution. The method is rapid, selective, economic and applicable to the removal of heavy metal ions from industrial waste water.IntroductionToxic organic pollutants and heavy metals ions mainly from industrial activities such as plating, metallurgy and dyeing industries, are a threat to human health and the surrounding environment, because of their toxicity and persistence after being released into the natural environment [1]. These pollutants must be removed or degraded to an acceptable level, before being discharged to the receiving waters. Therefore, detection and determination of heavy metal ions in industrial waste water is very important.Inductively coupled plasma optical emission spectrometry (ICP-OES) is the most used technique for the determination of heavy metal ions because of its capability for rapid multi-element detection over a wide concentration range and with relatively low detection limits. Compared to other techniques such as neutron activation analysis (NAA), X-ray fluorescence spectrometry (XRF) and inductively coupled plasma mass spectrometry (ICP-MS), ICP-OES has the above advantages. Some constituents in industrial waters, such as organic compounds and inorganic salts, may cause matrix effects. In order to achieve accurate and reliable results, an efficient preconcentration of heavy metal ions and their separation from the matrix are usually required."

Jan 1, 2012

By P. Chris Pistorius

Calcium treatment of alumina inclusions, to convert the alumina to molten or partially molten calcium aluminates, is a well-established treatment for steel, to improve the castability of aluminium-killed steel. However, the role of magnesium in calcium-treated steel is not fully clear, nor is the origin of the several percent of magnesium oxide that is often present in calcium-treated inclusions. To study this, steel was sampled after calcium treatment at an industrial steel plant, and the inclusions identified by energy-dispersive X-ray microanalysis (EDX) on polished sections of the samples (analysing the samples in a scanning electron microscope). The predicted fraction liquid in the inclusion was estimated from the ternary alumina-magnesia-lime phase diagram. Inclusions with higher CaO contents generally had lower MgO contents, indicating that the calcium wire is not the origin of the magnesium in the inclusions; this was also confirmed by wet chemical analysis of the calcium wire. Instead, it appears that magnesium-alumina spinel inclusions form during extended ladle contact after aluminium killing and before calcium treatment. While such spinels have been stated to cause poor castability (clogging the submerged-entry nozzle), it is clear that calcium treatment successfully modifies the spinel inclusions to mixed alumina-lime-magnesia inclusions, where the magnesia content contributes substantially to liquefaction of the inclusions: for typical MgO contents of around 10%, the range of Ca:O ratios which yield liquid (or partially liquid) inclusions is extended substantially to lower Ca:O ratios.

Jan 1, 2006

By Carlos Schvezov, Eliana Agaliotis, Alicia E. Ares, Mario Rosenberger

"The interaction between a solidification front and a spherical particle was modeled and simulated in order to study the phenomenon of ""pushing"". Finite element methods were employed in axisymetric domains. The drag force is calculated from the calculated fluid flow field and the repulsion force is the Lifshitz-Van der Waal force. The thermal field is decoupled from the force field. The model is applied to a metallic matrix containing particles with similar, lower or higher thermal conductivities than the matrix, resulting in planar, convex and concave interface shapes, respectively.The results show that the critical velocities for pushing for concave and convex interfaces are about one order of magnitude larger and one order of magnitude lower than the critical velocity for flat interfaces, respectively. The simulated results were in very good agreement with reported experimental results.IntroductionThe solidification interface of materials containing spherical particles in some cases can push the particle ahead the interface. This phenomenon generally occurs during the solidification of different materials such as, metallic alloys containing native particles, metal matrix composites containing particles or fibers as reinforcements and crystallization of semiconductor, optical, optoelectronic or biological materials. In all cases the interaction strongly determines the distribution of particles and the resulting physical and physic-chemical properties of the resulting material. The phenomenon has been investigated for many years both experimentally and by mathematical modeling [1-21]. The process is complex due to the variety of phenomena involved during pushing. In all cases, the physical problem depends on the properties, nature, and morphology of the interacting media; the particle, melt and solid; and external fields such as gravity, thermal and electromagnetic fields."

Jan 1, 2012

By Baokuan Li, Fang Wang, Meilong Shan

"As the advantage of uniform bus loading, the electroslag remelting (ESR) furnaces with three - phase installation by delta or star connection are mainly used to produce the large or super large ingot. The electrical efficiency is significantly improved as the short circuiting through the molten slag. However, little is found about fiindamental research on the electromagnetic field of the ESR system with three -phase installation. A three-dimensional (3D) finite element model was developed to simulate the current density, magnetic field, electromagnetic force and Joule heating for a system of electrode, slag and ingot in the ESR system with three -phase installation.IntroductionThe metallurgical performance of the ingot is the fundament and precondition to obtain the large forging of high quality, which has a critical role in the producing of forging. The electroslag process (ESR) to product the metal materials of high homogenization and clarity become more and more popular[1].The electroslag process is a special smelting technology of producing small ingots, which originate in 1950[2].At present the three, four or six electrode is used in large scale electroslag furnace. It has been found that the deeper molten pool and the wider of the two-phase zone with only one large diameter of electrode to product large ingot effect the solidification microstructure of ingot[3]. However, the molten pool becomes shallow relatively with several electrodes producing the large ingot, which is benefit to the solidification microstructure of ingot. Three electrodes electroslag remelting furnace take the three phase equilibrium power supply to making the load and electric power network balance, avoiding the distortion phenomenon induced by single phase power supply and saving electric power. It also can uniformize the distribution of heat source."

Jan 1, 2012

By Florian Kongoli

While calcium ferrite slags have been successfully used in continuous copper converting for the last 30 years, ferrous calcium silicate slag was proposed about 8 years ago as an additional alternative for copper smelting. Although both slags are normal extensions of each other their phase relations have not been completely clarified. In this paper the liquidus relations of both slags have been quantified at various areas that cover both of them. The existing experimental data have been first reviewed and discussed in relation to the solidification procedure. An original physical model is then used to predict various diagrams of the liquidus surface of both slags. It is shown that the ternary liquidus diagrams normally used for FeOx-SiO2-CaO system are not suitable for industrial slags. The new model diagrams of Fe/CaO versus SiO2 and Fe/SiO2 versus CaO as well as Fe/CaO versus Temperature and Fe/SiO2 versus temperature are proven to be much more convenient for ferrite and ferrous calcium silicate slags. Based on these diagrams the effect of SiO2 and CaO on the melting temperature is quantified. The effect of Cu2O is also quantified through the model. Some Fe/CaO versus Cu2O and Fe/SiO2versus CaO at various copper contents are predicted and the results show good agreement with the experimental data. It is also shown that in the presence of liquid copper, Cu2O is dissolved in the slag depending on the oxidation degree of the system and might lower the liquidus temperature. Some discussions are also presented taking into account plant observations and important conclusions are drawn for copper smelting and converting

Jan 1, 2006

By Li Zhang

A novel green technology to recovery Titanium compounds from Ti-bearing blast furnace slag under the dynamic oxidation condition was developed and tested. Air was blown into the molten slag as oxygen resource through a lance during the dynamic oxidation process, in which six important results were found: (1) The TiC, (Ti2O3), Fe and (FeO) in the slag were oxidized; (2) The temperature of slag temperature rapidly increased; (3) The viscosity of slag decreased; (4) The coalescence, growth and drop of the metallic Fe droplets in the molten slag were carried out under an air agitation condition; (5) The dispersed Ti components were selectively enriched into the perovslite phase, and the perovskite phase could be selectively precipitate and grow. And also, the perovskite phase can be separated by the dressing method. The oxidation of molten slag gives off a large amount of heat, which helps chemical reactions proceed, improve the rate of chemical reactions, and promote the precipitation and growth of the perovskite phase. The features of the technique are clean, low cost and a great capacity to deal with a large quantity of slag. It was confirmed by experiments that the precipitation of the perovskite (CaTiO3) in molten slag is obviously affected by operation factors such as temperature, chemical composition, heat-treatment, additives and so on. The precipitating kinetics and mechanism of the perovskite phase from molten slag during the dynamic oxidation processes were also investigated.

Jan 1, 2006

By Xiping Chen, Wangxing Li, Jiemi Zhou

"Desulfurization methods suitable for anode-grade petroleum coke (coke for short) used in primary aluminum industry are coke desulfurization during calcination, desulfurization in soakage and desulfurization in mediums. Coke desulfurization during calcination is discussed in this paper. Influences of calcination temperature, holding time and coke granularity on coke desulfurization were discussed. Experimental results show that calcination temperature has a remarkable influence on coke desulfurization. When the temperature is high enough desulfurization ratio of coke can reach 85% only by calcination. Holding time has a definite influence on coke desulfurization, but desulfurization ratio is low at the temperature of 900~1300°C. The influence of holding time is obvious when calcination temperature surpasses 1400°C. The influence of coke granularity is smaller compared with calcination temperature and holding time.IntroductionPetroleum coke is main raw material for carbon anode in primary aluminum industry, and its weight percentage in carbon anode is about seven percent. Green coke can not be directly used for anode production because of its immanent moisture and volatiles. Green coke must be calcined in order to meet the request of anode production. Calcination is a heat-treatment process during which green coke is heated to a given temperature to remove volatiles, moisture and some sulfur. Real density, strength, electrical conductivity and anti-oxidation ability of petroleum coke can be improved by calcination and calcined coke can be received [1, 3, 4]. Sulfur in calcined coke finally goes into carbon anode. During baking or aluminum smelting, the sulfur in anode ultimately changes into SO2 and emits from anode into the atmosphere. Excess SO2 easily leads to acid rain which brings heavy pollution to the environment [1, 2]. With the development of Chinese aluminum industry, consumption of anode-grade petroleum coke increases year by year, the total consumption in 2007 surpassed 4.5 million tones and the yearly emission of SO2 from aluminum smelters has exceeded 270 kilotones. From 2005 Chinese government began to limit the emission of SO2 from primary aluminum industry, so desulfurization of anode-grade petroleum coke becomes more and more urgent. Some relationship need to be found and used to guide desulfurization of petroleum coke."

Jan 1, 2008

By K. H. Ho

This paper describes a simplified numerical model which is used to study the skull formation of liquid metal on a rapidly rotating disc in centrifugal atomisation. The skull formation is one of the problems limiting the wide use of centrifugal atomisation. The enlarging skull on the atomising disc reduces the yield of metal powder produced and produces a resistance to the centrifugal force which worsens the quality of the powder. It is costly and often difficult to study the flow behaviour by experiments due to the complex heat transfer and phase transformation during the processing. Computer modelling is therefore a powerful tool for mechanistic understanding of centrifugal atomisation. This paper investigates the flow pattern of the melt on the rotating disc as a function of initial temperature, melt flow rate and disc rotation speed as well as the physical properties of the melt, such as density, surface tension and viscosity using the commercial package Flow-3D. Keywords: Solidification, Rotating disk, Centrifugal Atomization

Jan 1, 2003

By Alain Jardy, Valerio De Felice, Jean-Pierre Bellot, Ismael Lis Alves Daoud, Stephane Hans

"Gas-stirring ladle treatment of liquid metal has been pointed out for a long time as the processing stage mainly responsible for the inclusion population of specialty steels. A steel ladle is a complex three-phase reactor, where strongly dispersed inclusions are transported by the turbulent liquid metal / bubbles flow. We have coupled a population balance model with CFD in order to simulate the mechanisms of transport, aggregation, flotation and surface entrapment of inclusions. The simulation results, when applied to an industrial gas-stirring ladle operation, show the efficiency of this modelling approach and allow us to compare the respective roles of these mechanisms on the inclusion removal rate.IntroductionThe reduction of the weight of high performance materials together with the improvement of mechanical properties and the increase of the recycling of used metal are new challenges which emphasize the importance of metal cleanliness. Ladle treatment of specialty steels has long been described as the secondary metallurgical process mainly responsible for the non-metallic inclusion derived from the deoxidation process. The treatment is accomplished by blowing argon through one or more porous plugs for the purposes of desulphurization, minor composition adjustments, and inclusion removal. Gas injection is applied on routine basis to achieve both the stirring of the liquid bath (thermal and chemical homogenization) and the entrapment of the inclusions by the bubbles (flotation). Furthermore, the turbulence produced in bubble swarms enhances the probability of inclusion collisions and makes aggregation the first mechanism for particle removal. The physical processes involved in gas stirred ladles are numerous and complex owing to the three dimensional and multiphase (metal-gas and inclusions) nature of the reactor. Despite these difficulties, the population balance equations can be implemented in CFD code11'21 and combined CFD-PBM (computational fluid dynamics - population balance method) models are investigated for steel ladle processes13'41 and produce very promising results in terms of inclusion removal efficiency."

Jan 1, 2012

By Wen-Ming Chien, Vamsi Krishna Kamisetty, Amrita Mishra, Ivan Gantan, Prathyusha Mekala, Dhanesh Chandra

"The phase equilibrium and characterization studies by using high temperature X-ray diffraction (XRD) and differential scanning calorimetric (DSC) methods have been performed for binary organic thermal energy storage materials. The organic thermal energy storage materials undergo a solid-solid state phase transition before melting which stores large amounts of thermal energy. Two materials [tris(hydroxymethyl)aminomethane(TRIS) and 2-Amino-2-methyl-l, 3- propanediol(AMPL)] were used for this study. Binary samples of AMPL-TRIS were prepared to perform high temperature XRD characterization and DSC studies and the binary AMPL-TRIS phase diagram was developed. The high temperature solid-state phases of AMPL and TRIS were characterized as a disordered BCC structure. It was found there is virtually no solubility of TRIS in AMPL or vice versa below -75 °C. The maximum solubility of TRIS in AMPL is 11% TRIS at 75 °C. The eutectoid transformation was shown at 19%TRIS-81%AMPL composition and at a temperature of 75°C. Lattice expansion calculations on single phase of TRIS and AMPL have been performed.IntroductionThermal energy storage materials can store a large amount of heat due to the presence of thermal transitions from the orientationally ordered to disordered phases occurring before melting. These molecules (such as amine and alcohol derivatives of neopentane) can reorient as a whole about the central carbon atom to form orientationally disordered crystals (ODIC) and their spherical shape makes them reorient relatively easier. Thermal energy storage materials are becoming increasingly important as a renewable energy resource. These molecules undergo large changes in enthalpies at solid-solid transitions. The presence of these compounds with large enthalpy changes are identified as potential thermal energy materials and some of die applications are solar cell systems [1-3]. Binary mixtures have been found as a way to adjust the transition properties in addition to pure compounds [4]. Tris(hydroxyrnethyl)aminomethane (TRIS, C(CH2OH)3NH2) and AMPL, CH3C(CH2OH)2NH2) are two important thermal energy storage materials."

Jan 1, 2012

By Ludy C. Motta, Denise C. O. Nascimento, Sergio N. Monteiro

"Natural cellulose-based fibers are nowadays of growing interest for modern industrial composites. Relatively unknown fibers like piassava, curaua and gourde have shown promising behavior as reinforcement of polymeric composites. However, the hydrophilic characteristics of the natural fibers impair its adhesion to the normally hydrophobic polymeric matrix. Surface treatments can, in principle, improve this adhesion and the fiber/matrix interfacial strength. In this paper, the effect of alkali treatment of the surface of piassava (Atallea funifera) waste fibers was investigated in terms of the change in strength of epoxy composites reinforced with these waste fibers.IntroductionThe consequences of global warming and the increase in the price of petroleum are motivating the use of natural materials as substitute for energy intensive synthetic materials [1]. In particular, natural fibers obtained both, from cultivated plants such as jute, sisal, hemp and flax as well as from industrial waste such as sugar come bagasse and coir, are being considered to replace synthetic glass fibers [2,3]. These natural fibers, also known as lignocellulosic fibers, present the comparative advantages of being renewable, recyclable and biodegradable. Moreover, lignocellulosic fibers require less amount of processing energy and are neutral with respect to CO2 emission, which causes the atmospheric greenhouse effect responsible for the global warming [4]. Low cost is another important economical advantage of the natural fibers over the synthetic ones and the application of lignocellulosic is also associated with a lower wear of processing equipment and better finishing of molded components [5]. Moreover, for some fibers, properties such as the mechanical strength and impact resistance can be superiors to the corresponding properties of synthetic glass fiber [6]. The characteristics and properties of several lignocellulosic fibers are, nowadays being extensively discussed in the literature. It is beyond the scope of this work to comment on the hundreds of papers dealing with this subject. However, there are still less known fibers with great potential as engineering material that deserves investigation."

Jan 1, 2008

By Guodong Lai, Shixing Wang, Lijuan Chu, Jinhui Peng, Zebiao Zhang

"The beneficiation of poor manganese ores containing phosphate gangue is very difficult by conventional processes, because of the similarities in the physico-chemical properties of the constituent minerals. The shaking table gravity concentration process and concentrated strong acid selective intensified leaching process were used for dephosphorisation of Yunnan manganese ore. The leaching process was effective. The effects of intensified leaching time, solid-liquid ratio and particle size were investigated. The relevant leaching factors were optimized as -0.125+0.088 mm particle size with 68% nitric acid for 24 h when using a solid-liquid ratio of 1:1 at room temperature and atmospheric pressure. Under these conditions, the P/Mn ratio was reduced from 0.0107 to 0.0056, and the grade of manganese was increased from 12.32% to 42.76%. The dissolution of manganese during leaching was negligible.IntroductionManganese and its compounds are widely used in the iron and steel industry as deoxidation and desulfurization agents and as alloying additives [1-2]. Because of the increase in demand, low grade refractory manganese ores are becoming a new source. Many Chinese manganese ores are high in phosphorus, which cannot be used directly for metallurgical purposes. This occurs because phosphorus enters into the metal phase during smelting and its presence sharply deteriorates the mechanical properties of the metal [3-4].Kanungo and Sant [3] investigated the dephosphorization of phosphorus-rich manganese ores by selective leaching with dilute hydrochloric acid. They observed that leaching with dilute hydrochloric acid (0.1-0.6M) could reduce the phosphorus contents to the specified limit of 0.12%. Ye [5] investigated dephosphorization of high-phosphorus manganese ore of the Huayuan type. Using high intensity magnetic separation, roasting and leaching with acid for dephosphorization, as used in the industry, a 40.15% manganese concentrate with a P/Mn ratio of 0.0037 was obtained. Yimin [6] investigated magnetic separation followed by inverse flotation of high-phosphorus manganese ore, and found that the P/Mn ratio could be reduced from 0.046 to 0.002."

Jan 1, 2012

By J. H. Huang

In this investigation, the selective precipitation of cobalt and molybdenum from Co-Mo aqueous solutions was studied in order to recover efficiently valuable elements from industrial effluents generated from a novel electrodeposition of nanocrystalline Co-based alloys process and reduce the effluent impact on environment. It was found that the behavior of cobalt in aqueous solutions was substantially affected by the presence of molybdenum. When adding 11.6 to 46.6g/L molybdenum to a 50g/L cobalt solution, the co-precipitation of molybdenum and cobalt started to occur at pH value of 3-4. However, without the presence of molybdenum, cobalt could only be precipitated out of the solution at about pH 6. Most of the molybdenum was found in the solid phase when the solution pH reached 5. After further increasing pH to greater than 7, the molybdenum dissolved back into the solution. Cobalt kept precipitating as the pH increased. When the pH was greater than 7, most of the cobalt was present in the solid phase. The chemical and physical characteristics of the precipitated materials were investigated by SEM, XRD, AAS and EDX. It was revealed that the precipitate was initially present as cobalt molybdate oxide hydrate and subsequently transformed as sodium cobalt molybdenum oxide. With further increasing the solution pH, the precipitate was transformed into cobalt hydroxide. Further investigation implied that most of molybdenum was chemically tied to the precipitate produced at the low pH, yet at the same time, physically entrapped at the high pH. The paper also presents the influence of reaction temperature and time on the precipitation process and kinetics.

Jan 1, 2003

By Christine Wenzl, Andreas Filzwieser, Stefan Konetschnik

"The METTOP-BRX-Technology is a novel manifold electrolyte inlet, which allows improved productivity and production in new and existing tankhouses by achieving higher current efficiency and cathode quality, as well as using current densities higher than 400 A/m2. Two installation examples are shown: Montanwerke Brixlegg AG, Brixlegg, Austria (upgrade of existing tankhouse) and Xiangguang Copper, Yanggu, China (new tank house). Montanwerke Brixlegg AG has been using the METTOP-BRX-Technology since 2005, and converted half of the whole tankhouse to METTOP-BRX in 2011 in order to use a current density of more than 400 A/m2. Xiangguang Copper started up their second tankhouse in May 2011. This tankhouse was constructed in the same way as the existing tankhouse, but was designed for 292,000 t/a cathode copper (existing tankhouse: 200,000 t/a) by using the METTOP-BRX-Technology. This production increase is a consequence of a much higher current density, namely 410 A/m2, compared to 280 A/m2 in the old tankhouse.IntroductionCopper electrorefining has been practised for more than hundred years, the last big change being the implementation of stainless steel cathodes in the 1980s [1], In 2005, the METTOP-BRXTechnology was first introduced. This technology was developed jointly by METTOP and Montanwerke Brixlegg, Austria, and allows improvements in productivity and production in new and existing tankhouses in an economic way. The METTOP-BRX-Technology is a novel manifold inlet that allows improved tankhouse productivity by increasing current density and/or current efficiency while maintaining or improving cathode quality [2]."

Jan 1, 2012

By Milorad Cirkovic, Mile Bugarin, Vlastimir Trujic

"Industrial scale testing was performed in the plant-site of Bor Company. Charging sample was from 4-5 tons for each particular test. All operations in industrial scale investigations were carried out in one furnace. For the aim of successful realization of experiments, and primarily for safety and prevention the risk of toxic contamination the working environment, a plant was designed and constructed for cooling and wet dedusting of gases formed during smelting process, zinc removal and flame refinement of molten metal. For the requirements of industrial investigations a complete plant for cooling and wet dedusting of gases has been constructed for brass scrap processing. In this plant, the original ultra-sonic water spraying devices have been installed. The efficiency of such simplified system for gas treatment has been 98,6%. Introduction Permanent development of techniques and technology causes formation the considerable quantities of secondary raw materials that are much more relevant as the raw material base for many metals. Due to a fact that large quantities of metal, are concentrated in the waste materials, large consideration is given to this topic, and numerous technologies for this waste recycling are developed in the world nowadays. High energz price and permanent increase of metal price on the world market have made that secondary raw material tretament, for the aim of various metals production, becomes more and more relevant in the world. In comparison of metal production using enrichment and metallurgical treatment of primary raw materials, the non-ferrous metals production from secondary raw materials has a range of advantages, as well as: - Low level of capital investments, - High technological recovery of qualitative secondary raw materils, - Considerably low consumption of energetic resources regarding to the treatment of primary raw materials (ore and concentrate), - Reduced consumption of unrecoverable mineral resources, - Reduced enviroment pollution [1,6]."

Jan 1, 2008

By V. K. Handa

Sterlite Industries (I) Ltd. started its copper smelter in 1996 and worked through the common problems associated with smelter start-ups. Specific issues in the converter area included converter blower IGV problems, punching machine reliability, converter spitting, back collar burning, ,and short converter campaign life. With a very young and dedicated team of engineers and technicians, smelter management assigned teams of three to four members to work scientifically and systematically through each major problem area to recommend and implement appropriate solutions. The converter mouth was redesigned with respect to tuyere and metal height to eliminate spitting and back collar burning. The air line was changed in places to reduce the pressure drop. A new back-up compressed air line and vessel was installed to prevent tuyere blockage in the event of a blower trip or power failure. The converter mouth liners and bricking around the mouth was modified to eliminate metal leaking through the pouring lip Modifications to the punching machines were made to address specific problems and preventative maintenance practices were further streamlined and reinforced to ensure 100% availability of hot metal cranes, converter blowers, punching machines, and ID fans. Matte availability and matte temperatures were improved by streamlining the upstream ISA and Rotary Holding furnace areas. Implementation of a detailed training program for the converter operators significantly improved the operation and morale. Water-cooled double hoods and a third converter were installed as part of the smelter modernization plan. The new hoods dramatically improved hygiene in the crane aisle while the addition of the third converter posed new challenges for the same motivated group of crews with respect to flip flop operation to keep the idle converter hot and to maximize in-stack time, managing crane/ladle logistics, and managing revert generation. This paper describes the converter operation's journey from the initial days of long blowing times and large revert accumulations to present operations with two converter flip flop operation, and also describes the team work, constant focus on increasing productivity and reducing costs, and benchmarking.

Jan 1, 2002

By C. P. Broadbent

Due to growing .public awareness of environmental issues and greater sensitivity towards waste management, many countries around the world are implementing more stringent legislation governing the storage and disposal of hazardous wastes containing heavy metals such as As, Sb, Pb, Cd or Hg. These wastes can no longer be dumped without providing clear guarantees that the material concerned is environmentally safe and will not leach toxic elements to the surroundings. In the Netherlands the current dumping charge for chemical waste (i.e. worst category) is $280/t, and for industrial waste this cost reduces to $75/t. If the material can be reused there may be a small positive credit for selling it, for example discard slag as an aggregate to the construction industry. A number of (pyre)-metallurgical operations, mostly associated with the extraction of metals from sulphidic ores, produce arsenic residues in the form of As2O3 containing flue dusts and speises. If the flue dust is of high purity it can be sold, though many traditional uses are being substituted by other materials. In many cases upgrading the quality of the arsenical dusts is not possible for either technical or economic reasons. Traditional practice is to dissolve these dusts in acid prior to precipitation as ferric arsenate, which is at present classified by many countries as industrial waste and can be dumped. Recent work, however, has cast doubt on the stability of arsenates for disposal and alternative disposal routes have been investigated. Tests have shown that up to 10% (dm) As can be incorporated into "glassy" silicate slags with very low levels of arsenic leaching in the cooled product. Calcium arsenate was added to a range of synthetic and industrial slags from the system SiO2-FexOy-CaO-A12O3-AsmOn, under mildly oxidising conditions and quenched subsequently in water. It would appear that this represents an environmentally acceptable method for the disposal of many arsenical residues and there is some optimism that this method will be equally applicable to the disposal of other toxic metal residues.

Jan 1, 1994

By Tomoya Nihei, Hiroshi Hayashi

"A novel selenium removal process called Recycled Green rust/Ferrite Process is developed by MMC. In this process, a mixed Fe2+-Fe3+ hydroxide compound, green rust (GR), reduces selenate to elemental selenium, while GR is consequently oxidized to magnetite Fe3O4. Sequencing batch-mode experiment showed that the residual selenium concentration gradually decreased with the number of batch test increased. Stable selenium removal was achieved when the number of batch test exceed 15 times. Optimum selenium removal ratio reached 99.95% where initial Se concentration 2.1mg/L decreased to 0.001mg/L. Furthermore, the continuous feeding test carried out through a pilot-scale plant with a feeding capacity 600 L/hr. Approximately 860-hour-feeding test was carried out for the selenium-contaminated groundwater which had an averaged selenium concentration of 0.88 mg/L. Selenium concentration in the effluent from thickener maintained less than 0.01 mg/L (selenium removal rate of 99%) until a net operating time reached 800 hours.IntroductionJapan is one of the largest producers of selenium, and thus there are potential environmental impacts of selenium on soil and aquatic environments. The Mitsubishi Material Corporation (MMC) owns some real estate properties whose soil and groundwater was polluted by selenium and other heavy metals. These sites include former industrial plants: a smelter for nonferrous metal and a fabricating semiconductors and pigments. Selenium in aquatic environment commonly exists in four oxidation states, namely, VI, IV, 0 and -II. Selenate ion (SeO4 2-), the most oxidized form of selenium, and selenite ion (SeO3 2-) are highly soluble and mobile. Elemental selenium (Se0) is insoluble in water and therefore has much lower toxicity. Because selenium is carcinogenic and teratogenic at high concentration, the national effluent standard in Japan is fixed at 0.1 mg/L and the environmental standard at 0.01 mg/L. Although there are several selenium removal techniques, the most conventional process is coprecipitation with a ferric hydroxide because of its simplicity and low cost. It is known that selenite is adsorbed strongly on the surface of ferric hydroxide, but selenate is not. The low affinity of selenate on oxide mineral surfaces was demonstrated by the fact that selenate could be easily displaced by adding competing anions, particularly sulfate ion. Selenate removal from polluted water is one of the most difficult techniques, and more effective methods are desired. MMC developed a novel selenium removal process [1]. In this process, the concentrated slurry that contains Fe(II)-Fe(III) hydroxyl-salts known as Green Rusts (GRs) contributes to selenate removal. The main components of the iron precipitate in the reactor are GRs and their oxidation product, magnetite (Fe3O4)."

Jan 1, 2008

By A. P. Paiva

Studies focused on the recovery of precious metals by solvent extraction have recently increased. either to devise suitable solvents or to clarify the involved extraction mechanisms and kinetics. In this work, a comparison of the performance exhibited by triphenylphosphine (TPP), bis-(penty1thio)-ethane (BPTE) and triisobutylphosphine sulfide CI"I'BPS) in the extraction of silver from acidic chloride media is carried out. Extraction and stripping isotherms involving the three extractants are presented together with the results obtained on the selectivity of silver extraction against high contents of iron, copper and lead. Attempts to clarify the mechanism of silver extraction by TIBPS were performed by studying the distribution coefficient dependence on ligand and chloride concentrations. The effect of temperature on extraction and stripping is also considered. The interfacial tension for the system, measured with different concentrations of extractant in the organic phase, is analysed.

Jan 1, 1994