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By Xinghua He, Shujing Zhu

"In this paper, the chemical composition, the content and the leachability of heavy metals in dredged sludge are tested and analyzed. It is shown that the leachability of Pb and Cr exceeds the leaching toxicity standard, and so the dredged sludge is considered as hazardous waste and must be solidified. The effect of solidifying the dredged sludge by the hydraulic ash-slag cementitious composites is studied, and it indicates that the heavy metals can be well immobilized if the mass fraction of the dredged sludge is appropriate. The heavy metals are immobilized within the hydraulic ash-slag cementitious composites hydration products through either physical fixation, substitution, deposition or adsorption mechanisms.IntroductionDredged sludge is classified as a hazardous waste because it usually contains concentrated heavy metals and chlorinated organic compounds, as well as soluble salts, and is also composed of very fine particles. Moreover, inorganic pollutants are typically associated with soluble compounds, which are, therefore, highly leachable from dredged sludge when dredged sludge is contacted by a liquid medium[l1. Thus, dredged sludge must be stabilized in order to reduce its environmental impact on the final disposal site. The frequent means of dredged sludge disposal used include(!) Chemical stabilization (2) acidic extractionChemical stabilization is translating mobile heavy metals into low dissolution and low toxicity form through chemical reaction. The commonly chemical medicaments are sodium hydroxide, soldium sulfide, thiourea, EDTA. But Zhao et al [ZJ found sodium hydroxide is not fit for Pb stabilization, the other three are effective, but the chemical properties of sodium sulfide are not stable, thiourea and EDTA are very expensive, and so it is very difficult to apply them. Moreover, because of the complexity of heavy metal conformation and dredged sludge composition, it is very difficult to find a cheap and prevalent stabilization medicament in point[31 ."

Jan 1, 2013

By Katsunori Okaya, Gjergj Dodbiba, Hiroyuki Ono, Toyohisa Fujita, Seiji Matsuo

"In an attempt to raise the copper grade of Printed Circuit board (PCB) by removing other components, carbonization treatment was investigated. The crushed PCB without surface-mounted parts was carbonized under nitrogen atmosphere. After screening, the char was classified by size into oversized pieces, undersized pieces and powder. The copper foil and glass fiber pieces were liberated and collected in undersized fraction. The liberation of copper foil from the oversized pieces was also investigated. The copper foil was liberated easily from glass fiber by stamping treatment. Liberation rate of copper foil was high at high carbonized temperature. The experimental results indicated that 90% of oversized char was liberated and the copper foil recovery from PCB carbonized at 1073K was 110kg/t. The copper recovery from char powder by flotation was also investigated. 15% of the copper grade and 80 % of the copper recovery were obtained, whereas the removal rate of silicon was 55%.IntroductionWaste Electrical and Electronic Equipments (WEEEs) should be recycled because they have many kinds of valuable materials and most WEEEs include Printed Circuit Boards (PCBs). In Japan, about 30 km2 per year of Printed Circuit board (PCB) has been produced [1], PCBs are normally separated from WEEEs and picked up by hand and sold to non-ferrous metal market because PCBs include high grade of copper and other precious metal such as gold, silver and palladium [2]. However, PCB also has impurities such as silicon, aluminum and calcium which are slag materials in non-ferrous smelting process, and other harmful elements such as lead, bromine and antimony. Low grade PCBs are sold after removal of invaluable parts or sometimes land filled without any treatment"

Jan 1, 2011

By C. M. Acuna

Scarcity of high grade copper low impurity content ores is a reality and processing of low grade dirty concentrates is a need. In spite of this fact, innovative strategies have to be looked at to comply with day to day more stringent environmental regulations. From this perspective the production of matte grades over 70% in copper presents several merits, but it must be contrasted with the fractional distribution of impurities reporting to the condensed phases. Converting of white metal high in arsenic content results in moderate fraction of arsenic to gas, but high deportment to blister. Therefore, production of anode copper, as required by the electrolytic refinery, may result in several operational difficulties. Furthermore, by recycling the flue dust and slag produced in the smelting-fire refining cycle, the arsenic content in the feed to smelting increases and so does in the resulting anode copper. The Teniente Converter, as a smelting unity, has probed suitable for production of high matte grade near white metal composition but regarding distribution behaviour of impurities there is lack of reliable data, specially when processing concentrates over 1% in arsenic content. In the new scenario, i.e. low grade copper high arsenic content concentrates, to fully asses the merits of this technology the effect of matte grade, secondary materials recycling and arsenic in feed upon the distribution coefficient of arsenic between slag and matte, mainly, must be evaluated both from a theoretical approach and by use of industrial data. Based on available data correlations of distribution coefficient, matte grade and matte/slag ratios with arsenic in feed and copper content in slag are worked out. Based on these results suggestions as to matte grades facilitating to deal more efficiently with the handling of smelting byproducts are proposed.

Jan 1, 2006

By Thomas Schemmel, Bertram Kesseiheim, Helge Jansen, Uwe Kreme

"During the last decades the refractory life time of the different aggregates of the secondary aluminium production was improved significantly. However, each repair and installation of refractory material affects the operating schedule and can cause costs in the million range. The downtime of just one melting furnace generate costs of 100.000 to 400.000 $ per day. Besides cooling down of the furnace and its repair, the heating-up procedure accounts for the longest time of the shutdown. Usually, heating-up of low cement or ultra low cement castables takes 120 to 150 hours. In order to reduce such expensive downtimes Refratechnik developed a unique and novel product series: Nanobond. These materials can be heated-up in only a third of the usual time. This paper talks about the theoretical aspects, as well as the mechanical and physical properties and especially practical experience of using Nanobond.Theoretical Aspects and Laboratory ResultsCement containing castables such as RCC, MCC, LCC or ULCC are considered standard in many refractory applications. Over the years a wide range of possible raw materials and practical installation methods were developed. However, all of these cement bonded refractory mixes possess one main important drawback. Such materials are characterized by the hydration of the cement bonding. As a result the physical bonded and the hydraulic water has to be removed in a relatively complicated drying procedure. The hydraulic water specifically demands a very careful and cautious heating up procedure. Most of the dreaded steam explosions can occur at a furnace temperature of approx. 250 oC. [1] To avoid such destructions, the heating-up of a new lined or repaired furnace can be very complex and slow. Depending on the furnace or the casted part a drying time of several days with long curing times are common."

Jan 1, 2012

By Viviane Tavares de Moraes, Denise Crocce Romano Espinosa, Jorge Alberto Soares Tenorio, Adriana Johanny Murcia Santanilla

"Increasing volumes of solid waste are generated worldwide, due to the continuous technological advances, the electronic scrap is part of these waste, requiring the study of recycling processes to stimulate this activity or the reuse of its components. The separation of nickel from sulphate leach solution, which also containing iron, zinc and aluminium was carried out using bis-(2,4,4-trimethylpentyl) phosphinic acid (Cyanex 272) as extractant, in order to determinate the effects of pH and temperature. The number of stages required for extraction was also assessed. The results showed that the metal extraction increased with increasing pH. On the other hand, increasing temperature was not favorable for all metals. However, under conditions used in this paper the purification of solution containing nickel was possible.IntroductionIncrease in the demand of metals in the world for use in industry causes a great exploration of natural resources. One outcome of this is increased investigations for the recovery of metals from industrial wastes. Nickel is found in wastes, such as batteries and electric and electronic devices, this kind of waste becomes a significant source for metals recovery. Since nickel is also present in printed circuit boards, which are associated with electric and electronic equipment, it can be recovered from this kind of waste through different techniques. It is important to highlight that iron is generally associated with this scrap [1] and for its removal chemical precipitation is often used. On the other hand, the solvent extraction process is widely used for treatment of leach liquors, because it can be produce high purity solutions [2, 3]. This technique is based on the purification of solution using contact between a liquor leaching and the immiscible organic solution, which contains an extractant that promotes the desired metal transfer [4]."

Jan 1, 2012

By M. K. Patel, K. A. Pericleous, M. Molaei

"The future trading of carbon credits and increased financial cost necessitates substantial cuts in incidental C02 emissions in the production of metals (iron, steel, aluminum, zinc, lead). Although greener methods of production are being developed, in the short term the use of point-source C02 extraction using existing technology remains attractive. Accelerated natural carbonation, in a fluidized bed is a feasible technological route investigated in this research. CFD modelling has been used to study the efficiency of C02 capture in a fluidized bed reactor containing a CaO solid sorbent. A Lagrangian/Eulerian scheme describes describe CaO particle trajectories and exchange of mass, momentum and energy with the carrier gas, with a typical off-gas composition. Different reactor geometries are considered (with uniform, stepped and gradually expanding cross-section), to maximize conversion for a given particle loading and size distribution (100-200 microns). Removal efficiencies of up to 80% are demonstrated, making this a viable process.IntroductionBased on Intergovernmental Panel on Climate Change (IPCC) reports, the major cause of climate change and global warming is due to a high level of C02 concentration in the atmosphere resulting from fossil fuel combustion, particularly in coal-fired power plants [1]. Carbon capture and storage is therefore the most important action proposed to reduce C02 from combustion flue gases. In this process, carbon dioxide is captured and may then be regenerated as pure C02 and conducted to a permanent storage, or simply stored as a solid carbonate [2]. Capture and storage of C02 has an economic penalty and the main cost of this penalty is associated with the capture plant. Capturing C02 with a lime-based solid sorbent (CaO) is a very promising technique, due to the low cost and the wide availability of the reactant. In this process, the CaO reacts with C02 based on the following reaction in a reactor called a Carbonator:"

Jan 1, 2012

By H. J. Thevik, A. K. Dahle

"A mathematical model that calculates the stress development in a coherent and stationary dendritic network due to interdendritic flow is proposed. The fluid flow is assumed to be related to the solidification shrinkage, and under the assumption of no porosity formation and unidirectional solidification, the shrinkage-induced flow within the mushy zone is calculated analytically. The interdendritic melt flow exerts a force on the solid network and an analytical expression for the stress build-up in the network is developed. Parameter studies illustrating the influence of cooling conditions, mushy zone length, dendrite coherency, fraction solid, volume fraction of eutectic, and solidification shrinkage upon the stress development within the solid network are presented. Comparing the magnitude of the calculated stresses to measurements of the strength in equiaxed mushy zones shows that it is possible for the stresses to exceed the strength, thereby resulting in reorientation or collapse of the dendritic network.IntroductionInterdendritic fluid flow is at present regarded as a very important mechanism for feeding of shrinkage during solidification of metal alloys. Solidification of many alloys is often characterised by heterogeneous nucleation of the primary phase on substrates in the melt with subsequent evolution of equiaxed dendrites. These equiaxed dendrites can initially grow freely, but impinge on each other and form a continuous dendritic network, ie. dendrite coherency, quite early in the solidification process. Measurements of the dendrite coherency point have shown that the dendritic network is established at solid fractions ranging between 0.1 and 0.5, and most often around about 0.2 [l]. Depending on the alloy composition this means that as much as 70 to 80% of the volumetric shrinkage has to be compensated by flow of liquid through the interdendritic network. Interdendritic flow occurs with a much larger resistance compared to free flow of the liquid and flow of a liquid with dispersed crystals. The pressure drop associated with the interdendritic flow increases rapidly with decreasing fraction ofliquid."

Jan 1, 1999

By Leiv Kolbeinsen, Stian Seim, In-ho Jung

"The current work presents new experimental data in the iron-unsaturated region of the FeTiO3-Ti2O3-TiO2 slag system. The samples are prepared by melting pure reactants in a high frequency induction furnace that employs a cold crucible. A similar experimental set-up has been described in literature and proven suitable to investigate high titania slags. The FeO content of the samples range from 3.7 to 21.8 wt% and the Ti2O3 content range from 3.6 to 30.1 wt%. The liquidus temperatures of the samples are measured in-situ by a spectropyrometer and range from 1450 to 1645 °C.In addition, an improved thermodynamic database for the FeO-Ti2O3-TiO2 system has been developed. Ternary parameters have been included and optimized to fit previously published experimental data. This optimization minimizes the discrepancy between experimental data and thermodynamic calculations as previously discussed in literature. New liquidus projection plots are proposed for the FeO-Ti2O3-TiO2 and the FeTiO3-Ti2O3-TiO2 systems.IntroductionIlmenite (FeTiOs) smelting is a relatively small industry world-wide. However, a reasonable focus on the process has been applied in Norway due to the location of one such smelter in Tyssedal, which is located in the western part of Norway. The process is essentially carbothermal reduction, where most of the iron in the ilmenite is reduced to its metallic state, and the titanium oxide is concentrated in the slag product. The metallic iron is sold as a high purity pig iron and finds applications in cast products. The slag concentrate is further processed for the production of TiOvpigment and/or titanium metal. This further processing can be performed through different routes according to the purity of the slag concentrate."

Jan 1, 2012

By T. T. Chen

Secondary copper anodes are generally rich in Sn, Pb, Ni and Sb, but are notably deficient in Se, Te and Ag. In the secondary copper anodes, most of the Ni, virtually all of the Ag, slightly more than one-fifth of the Pb, about one-third of the As and Sb, and approximately one-tenth of the Sn are in solid solution in the copper. The remaining impurity contents occur as 1-5 µm grain-boundary inclusions in the anodes, and these are mainly Cu2O, SnO2, Cu-Pb-As-Sb-Bi oxide, Pb-Sb oxide, Sn-Ni-Zn oxide, Cu-Sn-Ni oxide, Cu-Sb-Ni oxide (Kupferglimmer) and trace Cu2(Se,Te). Barium sulphate, which originates from the mold wash used in casting, is also present in the anodes. During electrorefining, the BaSO4, SnO2, Pb-Sb oxide, Sn-Ni-Zn oxide, Cu-Sn-Ni oxide and Cu- Sb-Ni oxide inclusions are liberated and accumulate in the slimes layer. Solid solution Ni dissolves and the Ni accumulates in the electrolyte. Solid solution Sn and Pb dissolve, but partly reprecipitate as Sn arsenate and PbSO4, respectively. Solid solution Ag dissolves but rapidly reacts to form Ag2(Se,Te), Ag powder, Ag-bearing Cu2O, (Cu,Ag)SO4 or a complex oxidate phase. Partial dissolution of the Cu-Pb-As-Sb-Bi oxide particles takes place; the Pb component is converted to PbSO4, whereas Cu, As, Sb and Bi dissolve. The reacted particles retain the morphology of the original Cu-Pb-As- Sb-Bi oxide phase. Some of the solubilized As, Sb and Bi remains in solution, but much reprecipitates as SbAsO4, As-Sb-Bi oxide, and as a poorly defined oxidate phase which consists mostly of Cu-Ag-Pb arsenate-sulphate. The high Sn contents of secondary copper anodes do not seem to affect the behaviour of the anodes during electrorefining.

Jan 1, 1999

By Lijuan Li, Zheng Lu, Xin Xia, Qijie Zhai, Qingchun Li

"Pulsed current and pulsed magnetic field have been applied to the bainite transformation of Cr5 steel. Three groups of experiments were conducted. In the first group, ordinary resistance furnace was used for heat treatment. The Cr5 specimens were rapidly heated up to austenitization temperature 940 °C, held for 20 min, air cooled to bainite transformation temperature 350 °C, held for 10, 20, or 40 min and then air cooled to room temperature. The second and the third group shared the same temperature-time curve with that of the first group, but their heat resources came from the Joule heat produced by pulsed current. 1.5 T pulsed magnetic field was exerted on the third group specimens when they were held at 350 °C, but the second group specimens did not undergo the treatment of magnetic field. It was found that both pulsed current and pulsed magnetic field obviously retarded the bainite transformation. The phenomena were discussed in terms ofliterature results.IntroductionApplying pulsed current and pulsed magnetic field technology are very pronnsmg ways to change the microstructure of materials by affecting the phase transformation process. People had found that pulsed current dramatically influences the behaviors of materials, for example, electromigration effect [l], the solidification of metals and alloys [2, 3], electroplasticity [4, 5], crystallization of amorphous alloys [6], healing of metal materials [7] and so on. As to pulsed magnetic field technology, a lot of effort had been spent on grain refinement in solidification of metals [8, 9], recrystallization of cold-worked metals and alloys [10] and Fe-based alloys solid-state phase transformation [11, 12]. Though application of pulsed current and pulsed magnetic field technology have proliferated in recent years, investigation on their effects on solid/solid phase transformation, especially bainite transformation, is lacking. The aim of this paper is to show the effects of pulsed current treatment (C-T) and the combined treatment of pulsed current and pulsed magnetic field (CM-T) on bainite transformation of commercial Cr5 steel"

Jan 1, 2014

By Chu Bo-Yi

"This paper contains a comparison of creep-feed and shallow-cut grinding on ceramics with both neat oil and water-based grinding fluids. When a water-based grinding fluid was used in creep-feed grinding on ceramics the vertical forces and specific energies increased markedly fast with result that the wheel surface was damaged seriously. Creep-feed grinding on ceramics with neat oil not only produced much lower grinding forces and specific energies but also resulted in the wheel remaining in good condition and minimizing damage to the ground surface. This finding may lead to a deeper understanding of the behaviors of grinding fluids in grinding processes both on ceramics and metal as well.1. IntroductionAs advanced ceramics are obtaining more and more applications in the technical area, some machining processes are needed after the sintering to reach the accuracy and finish required by components. Because of higher hardness and brittle behaviors of modem ceramic many researches have been done in order to improve grinding efficiency and surface quality.In the grinding metals the concept of creep-feed grinding has been developed in industry as a real alternative to the normal method of shallow-cut grinding. In addition to the general economic advantages, dimensional accuracy and surface integrity are invariable improved using the creep-feed grinding technique.In grinding ceramics former studies have done many works on both creep-feed and shallow-cut grinding on ceramics with water-based grinding fluids since the water-based were thought to be better coolants than neat oil in most tests of grinding metals[l]. It was suggested that the specific grinding energies of ceramics are markedly higher in creep-feed grinding. The grinding force increases vary rapidly with time in the creep-feed case. In other words, so-called speed stroke grinding with high workpiece speed is considered more suitable for improving the grinding efficiency [2][3]."

Jan 1, 1998

By Anil Saigal, Jr. Fuller, Said Jahanmir

"All-ceramic crowns, including glass-infiltrated spinel composites, are coming into widespread use because of their superior aesthetics and chemical inertness. This study investigates the residual stresses that are developed in these composites as a result of cool down from the glass-infiltration temperature to room temperature due to slight mismatch in the coefficients of thermal expansion and its effect on the mechanical behavior of these composites. Two-dimensional finite element simulations were performed using an object oriented finite element program OOF. The OOF program is a combination of two programs. The first program, PPM200F, is designed to read an image file such as a micrograph. The individual pixels that constitute the micrograph may be collected into groups and their material properties assigned. PPM200F is then used to create the finite element model/mesh that OOF then reads. The average residual stresses are found to be tensile in the spinel matrix and compressive in the infiltrated-glass. There is large variation in residual stresses and strains from location to location with presence of locations at which the glass is under tensile stress. The crack initiation and initial propagation in glass-spinel composites is at the glass-spinel interface in both the glass and the spinel. The presence of residual stresses can lead to lower crack initiation stresses and degrade the mechanical properties of the composites.IntroductionGlass-infiltrated spinel ceramics are in clinical use as core materials in all-ceramic crowns and as inlays and onlays (1-3). Advantages of ceramic composites include near net-shape forming with high strength in the infiltrated state. Besides, spinel is quite translucent and may potentially be used without a veneer. However, these ceramic composites are subject to damage accumulation from repeat oral contact loading and often fail after a few years of use (4). This paper examines the residual stresses that are developed in these composites, after cooldown from the glass infiltration temperature to room temperature, due to the slight mismatch in the coefficients of the thermal expansion of the two phases."

Jan 1, 2001

By H. Sieber

Multilayer samples of tantalum and aluminum with the composition of Al-25Ta were prepared by cold rolling of elemental foils. The microstructure and phases were characterized by XRD, SEM and TEMISAED and the reactive phase formation was examined by DSC and DTA measurements in multilayer foils rolled for different deformation levels. The rolling procedure yields a decrease of the Ta particle size in the Al matrix and also results in the formation of a multilayer structure with a thickness of the elemental foils down to 200 nm in average. No phase formation is observed during the cold rolling procedure. While XRD and DSC measurements show no phase formation up to the melting of aluminum for samples rolled up to 40 F&R (fold and rolling) passes, in samples rolled for 50 or more F&R passes a first phase formation reaction yield an interfacial layer of TaAl3. Contrary to former studies in the investigated cold rolled Al- 25Ta multilayers the reaction starts at temperatures as low as about 340°C. The first stages of the reaction are associated with two exothermic maxima, that increase in amplitude and shift to lower temperatures with increasing number of F&R passes. At higher temperature the TaA13 reaction layer thickens very sluggishly and yields a third exothermic maxima at about 600°C. Isothermal DSC scans show the reaction is not finished for samples containing elemental particles larger than 1 pm after annealing at 550°C for 5h. In all the investigated samples no Al- Ta phase other than Tad3 was observed to grow for heat treatments up to 800°C. Multilayer samples heated up to 1400°C show a morphology consisting of small AITa2 particles embedded in a single phase TaA13 matrix. The multilayer microstructure and reaction product morphology are characterized by SEM and TEM investigations in cross-section and plan view geometry.

Jan 1, 1998

By Zhiqian Zhang, Chao Wu, Chao Li, Hongxu Li, Yu Chen, Xiangxin Hao

"In this paper, the life cycle assessment models for automobile lightweight materials including high-strength steel, aluminum alloy and magnesium alloy are developed by Gabi software. The evaluation models and evaluation indicators such as acidification effects, rich eutrophication effect, ozone layer depletion effects, global warming, resource consumption and formation of ozone potential were taken into account. It is shown that the effects of acidification and ozone formation are mainly derived from the run phase of high-strength steel and they have strong environmental impact load. While considering the entire life cycle with materials production phase and resource consumption, the aluminum and magnesium alloy appe art o have large r environmental load than high-strength steel. Base d on the evaluation, some optimization tips are proposed.IntroductionAs the increasing of car ownership, automobile has its two sides. One which is the convenient, efficient and fast traffic vehicle; the other is aggravating energy consumption, emissions and environmental pollution. The car industry faces heavy pressure with energy saving, safety and environmental protection. Nowadays, the main study ways for automotive energy-saving and environmental protection are power system improvement, alternative energy sources and technologies. For limitation of technique, development cycle and market share, the development of car is little progress at this stage and the application has been restricted. And another important way is the lightweight of vehicle. Usually there are three ways to get the lightweight automobile body structure, automobile body structure optimized design, using advanced body manufacturing technology, development and application of lightweight high strength body material.The life cycle assessment (LCA)[1lis commonly used to evaluate environmental factors and potential environmental impacts of products and services. As an environmental management tool of product-oriented, it becomes increasingly popular in industry. In this study, the concept of LCA and GaBi software was used to develop models for the three automotive lightweight materials, evaluate the environmental impact and make horizontal and vertical contrast by choosing variety of evaluation systems and indexes."

Jan 1, 2013

By Robert W. Bartlett, Keith A. Prisbrey

"Natural biooxidation of shallow, refractory ore heaps, relying on gaseous oxygen diffusion from the heap surface is attractive because of its simplicity and potential low cost, especially without using a lined pad, which is possible if percolation of leachate through the heap is avoided. In this case, the excess oxidation enthalpy must be removed by water evaporation from within the wet ore heap, and the rising water vapor flux within it will impede the downward oxygen flux. An analysis of this process shows that for typical values of pyrite grades and limited temperature increases in the ore heap, the oxidation rate and penetration into the heap is reduced to values between about 30 percent and 50 percent of those obtained when leachate percolation occurs and water evaporation is not a significant mechanism of heat removal.IntroductionHeap biooxidation of refractory gold ores, needed as a pretreatment step to liberate the gold for subsequent extraction by leaching, requires large amounts of oxygen for the normal amounts of sulfide minerals that are typically present, one to two percent pyrite and/or arsenopyrite.The importance and potential limitations of oxygen transport into commercial ore heaps, which are much larger than encountered with column tests of ore and with pilot heaps, has been recognized111 • Commercial ore heaps using radial stacking conveyors are typically about nine meters high and may be 100 meters or more in lateral dimension. Three oxygen transport mechanisms have been identified and analyzed: ( 1) natural convection, which arises from an increase in buoyancy caused by the temperature rise and gas composition changes associated with the exothermic oxidation of the sulfide minerals within the ore heap, (2) forced air ventilation, using low pressure fans and air distribution pipes within the heap, and (3) diffusion of oxygen in the gas-filled void spaces within the ore heap driven by the oxygen concentration gradient from the surface of the heap to the mineral oxidation loci within it."

Jan 1, 1997

By Yongyong Gong, Qijie Zhai, Zhichen Zhang, Qixin Li, Zhishuai Xu

"Microstructure of semisolid slurry of Al-4.5wt.%Cu alloy was investigated with pulse magnetooscillation (PMO) treatment, the results showed that the PMO treatment can refine the crystal structures of Al-4.5wt.%Cu alloy significantly. The discharging frequency of PMO had a great effect on the solidified structure transformation of semisolid slurry of Al-4.5wt. %Cu alloy, and the primary a-Al particles become much finer and rounder with an increase of discharging frequency. However, over a certain discharging frequency, the grains of primary a-Al become coarse.IntroductionOver the last decade, a lot of attentions have been paid on metal rheoforming process [1-4], since it has higher mechanical properties of formed components, strength to weight ratio and age hardenablity. Nevertheless, semi-solid forming is always performed at high solid fractions (40%-60%), so it has the limitation of viscosity, a tends to be difficult to pour semisolid slurry into the hole of the shot sleeve. Therefore, a series of novel semi-solid slurry preparation methods and rheoforming techniques have been invented, such as, semisolid vibration treatment [5], rheocasting [6], pulsed magnetic field process [7], annulus electromagnetic stirring [8], via ultrasonic vibration process [9], equal channel angular extrusion (ECAE) process [l0] and straininduced melt activation (SIMA) process [11].The electromagnetic field is characterized by its effective grain refinement, green, convenient manipulation and without contamination of melt. The mechanisms of dendrite was fragmentation by electromagnetic field have also been largely proposed [12-14]. The broken dendrite arms then undergo a coarsening process to provide the globular structures and obtain much finer and rounder a-Al particles. When compared with other external electromagnetic techniques, Pulse Magneto-Oscillation (PMO) has obtained more fuvors, owing to narrower pulse width and much lower energy consumption. Furthermore, the PMO treatment can reach finer grains with shorter time treatment [16, 17]. This work aims to study the effects of different discharging frequency ofPMO treatment on the microstructure transition of the semisolid slurry of Al-4.5 wt.%Cu alloy."

Jan 1, 2014

By Daniel Chen, Jewel Andrew Gomes, Venkata Palla, Sadia Afrin Jame, David Cocke, Paul Bemazzani

"Textile industries use various kinds of chemicals including dyestuffs and pigments during dyeing and finishing processes. The effluent from these processes includes suspended particles, strong color, high pH and high chemical oxygen demand (COD) that are extremely toxic and make environmental hazard. Although physical, chemical, photochemical, and biological methods are available for treating such wastewater, the electrochemical technique, electrocoagulation (EC), has emerged as an efficient, simple, and cost-effective technology in the last few decades. In this study we present the applicability of EC technique for removing dye, such as direct red dye using iron electrodes, and the optimized conditions such as dye concentration, current density and pH. The degradation of dye molecules was investigated using UV-visible spectroscopy. The EC-floe was also characterized using SEM/EDS, XRD and FTIR.IntroductionWastewaters generated by textile industries contain large amounts of toxic aromatic compounds, especially azo dyes. Azo dyes and their degradation products, such as aromatic amines, are highly carcinogenic. These effluents are also responsible for causing high levels of color. The colored wastewater released into the environment is also a source for disruption of aquatic life and aesthetic pollution as well [1].In most textile industries, dyeing and finishing are the two important processes which are generally applied. These two common processes generate significant amount of wastewater, which may contain, suspended particles, high pH, strong color and high chemical oxygen demand (COD) concentration [2]. Low pH and high temperature are other polluting factors from the waste water. Textile industries make use of about 10,000 dyes and pigments [3]. Disposal of these colored wastewaters poses a major problem for the industries as well as a threat to the environment. In textile industries, because of the low efficiency (60-90%) of dye fixing on textile fibers, substantial amounts of unfixed dyes are released in waste waters. The conventional method for treatment of textile wastewater was a combination of biological, physical and chemical methods [2]."

Jan 1, 2011

By Baicheng Liu, Houfa Shen, Wensheng Li

"In order to understand the formation of macrosegregation in steel ingots, a mixture model has been developed which accounts for coupled mass, momentum, species, and energy transport to describe the sedimentation of free equiaxed grains during solidification. In this model, the mushy zone is divided into the slurry and porous regimes according to a solid packing fraction. Settling velocity of equiaxed grains in the slurry regime is given by an explicit expression. The solidification of a binary steel ingot (Fe-0.36wt.%C) with a two-dimensional geometry is numerically simulated. It is demonstrated that the predicted macrosegregation patterns agree to some extent with classical experimental results. Further refinement of this model is still necessary for realistically simulating steel ingot solidification.IntroductionModeling macrosegregation in steel ingots is still a challenging study, mainly due to the length scale of the products and the complexity of global multiphase transport phenomena coupled with microscopic solidification kinetics [l]. The thermal-solutal convection and the motion of equiaxed grains are the two main mechanisms responsible for macrosegregation. But there are few models that deal with the motion of equiaxed grains, which is confirmed as the main phenomenon that explains the negative macrosegregation along the centerline of large steel ingots [2]. A model which takes into account melt convection and grain sedimentation was first proposed by Beckermann and co-workers ([3], and references therein). More recently, similar multiphase solidification models with advanced nature have been presented by Wu and Ludwig [1,4] and Combeau and co-workers [5,6]. It is known that the application of these sophisticated models to steel ingot casting is at its beginning.In this paper, a solidification model based on continuum mixture approach, using much less sophisticated relations to obtain the settling velocity of free equiaxed grains, has been proposed in order to predict the macrosegregation in steel ingots. The model is applied to simulate the solidification of a binary steel ingot with a two-dimensional geometry, and preliminary modeling results are presented."

Jan 1, 2011

By Guolin Zheng, Tiejun Chun, Jian Pan, Deqing Zhu, Xianlin Zhou, Dong Chen

"The high temperature oxidizing-chloridizing roasting is one of useful methods to separate nonferrous metals from pyrite cinder and metallurgy slag. However, as one kind of main nonferrous metals in pyrite cinder and metallurgy slag, copper’s chlorination behavior is not demonstrated. In the present study, chlorination behaviors of CuO, Cu2O and CuS at the temperature range of 1025-1175 ? in air by simulating the chloridizing roasting process of pyrite cinder and metallurgy slag have been investigated. It is shown that Cu2O and CuS is much easier to remove, CuO is refractory to remove. In addition, the presence of SiO2 and CaO increases the Cu removal rate from CuO while the presence of SiO2, Al2O3, CaO and MgO decreases the Cu removal rate from Cu2O. Fe3O4 influences the Cu removal rate from CuO and Cu2O positively.IntroductionAs two kinds of significant secondary resources, pyrite cinder and metallurgy slag contain not only abundant iron but also considerable copper, lead, zinc etc. Millions of tons of pyrite cinder and metallurgy slag were discharged from nonferrous metal and chemical industries annually [1, 2] in China. The pyrite cinder and metallurgy slag are formed by roasting of minerals at a high temperature, so the properties of them are distinctly different from the natural iron ores, and the iron in them is closely associated with copper, lead, zinc and other nonferrous metals. High-quality pyrite cinder and metallurgy slag containing high iron and low impurities can hardly be obtained, leading to their low utilization degree [3]. Chlorination is characterized by the high reactivity of chloridion, the high volatility and low melting point of metal chlorides, and the big differences in the formation of metal chloride. Therefore, chlorination is widely applied in extraction metallurgy."

Jan 1, 2012

By William J. Mallio

Substantial differences between in situ and conventional technology require that in situ ore grade be established for deposit as distinct from the total contained metal value. Establishing an in situ ore grade involves determining the fraction' of the contained metal that can be leached by the fluid. This depends on the proportion of the ore minerals that occur on fluid flow paths as defined by the permeability distribution. Mechanisms involved in the in situ mining of sulfides are: oxidation of the sulfur, solution of the metals, complexing of the released metals, and a transport to a recovery point. Metal ions may be delayed or lost due to inefficiencies in these pro-cess steps or by reactions of the metal ions in solution with the rock. These reactions can involve precipitation of new phases, exchange of the metals of the interest with Ca or Na in clays or zeolites, retention of metals in oxidized mineral grains, or secondary enrichment of other sulfides along the paths of the solution flow. The efficiency of solution of metals and potential loss or delay mechanisms are controlled by local equilibria (the Eh, pH conditions) present in different parts of the ore zone. Permeability distribution in the rock mass and the coincidence of ore minerais with flow channels must be determined before a deposit can be judged suitable for in situ mining. Laboratory studies indicate that the natural permeability system is dependent on the degree of cementation of veins by late generation hydrothermal activities. The major conclusions of the study are:, 1. Deposit selection is critical; suitable deposit types include deep lying sedimentary deposits, selected zones of porphyry systems and vein controlled hydrothermal deposits; 2. Adequate laboratory and geochemical analyses should be undertaken through quantitative petrographic study and permeability mapping; and 3. Economic incentives for in situ mining must consider limitations of recovery caused by inefficiencies in dissolution and transport associated with particular deposits.

Jan 1, 1981