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By Tarek M. Abd El Hamid, Suzane Ali

"Treatment of industrial waste materials is created serious problem in Egypt. Aluminium sludge is generated as a by-product from aluminium household industry which contains significantly high alumina content exceeding 90%. This by-product randomly disposed and creates serious environment problems to locate community. To develop the treatment process of this material, the recovery of high purity alumina and identify the potential application is being the primary objective, This paper represents the recovery process of alumina process waste sludge High purity alumina material <99.8% aluminium oxide with originate particle size 0.125-0.420mm and apparent density 0.39g/cm3 was obtained with a specific surface area 139m2/g. Alumina produced was modified by cerium oxide doped alumina. The catalytic activity and selectivity was investigated in conversion of iso-propanol via dehydrogenation reaction yielding only acetone indicating an excellent selectivity the dehydrogenation. The presence of 10% CeO2 increase in the catalytic activity of 82% for the originated alumina. Introduction Approximately 20 thousand tons of aluminium waste produced in Egypt in 2006 with increasing amounts expected in succeeding years. A part of this waste contains organics impurities which coexisted with aluminium waste as a result of manufacture final aluminium products, waste usually content <1 to 2 wt% of organic carbon. It's generally admitted that the organic species are present in the form of lubricant oils used in rolling and pressing equipments for aluminium sheet. Both industry and government face possible high-cost disposal problems that more magnified by large volume of waste produced. The alumina recovery leachable study conduct in this paper had the following objectives: 1- Develop a process that can provide an environmentally acceptable residue and also recover the available alumina. 2- Evaluate the alumina produced in terms of grade and catalytic application."

Jan 1, 2008

By Ning Wang, Bing Xie, Hong-Yi Li

"Compared to traditional sodium roasting, calcified roast inhibits chlorine pollution. A vanadium extraction technique based on a calcified roast is especially suitable for vanadium slag with high calcium content. In this report, V205was extracted from vanadium slag by calcified roast followed by acid leaching and hydrolysis precipitation. In optimized conditions, the high silicon low vanadium slag was roasted at 850'C for 2 hours without CaO addition. The roasted materials were leached with 35 % H2SO4 in liquid/solid ratio of 5:1 (mL/g) at 95OC for 4 hours. The extraction of vanadium was as high as 97.66 %. These results are instructive to V2O5 production in industry.IntroductionVanadium slag is produced in converter, sodium salt roasting is the commonly used technique to extract vanadium. In sodium salt roasting, vanadium slag is roasted with sodium salts including sodium chloride and soda as additives, followed by leaching with acidic or basic solution [1]. However, in this process chloride reacts to produce corrosive gases including HC1 andCl2- SO2 and SO3 can also corrode equipment severely and are also an environmental contaminant. The low melting point of sodium salts leads to fusion agglomeration, which blocks vanadium oxidation and thus decreases the extraction rate of vanadium. A large amount of sodium salts consumed as roasting additives increases the production cost. Moreover, sodium salt roasting requires low CaO content in vanadium slag. When the CaO content increases to 1%, V2O5 extraction can amount to 4.7%-9% [2]. For vanadium slag with high CaO content, the sodium salt roasting technique leads to low vanadium extraction rate."

Jan 1, 2012

By Anatoly Sudnev, Vladimir Skorohodov, Igor Kudryavtsev, Boris Radionov, Dmitriy Panov

"In cobalt production technology at a stage of solutions purification manganous cake (slime) basically containing hydroxides of the specified metals is formed. The possibility of full cobalt recycling in the basic technology of metal production at slime processing with generation of pure manganous compounds is shown. After slime dissolution in sulfuric acid in the presence of reducers the solutions containing cobalt, manganese, nickel and other nonferrous metals are formed. Optimum conditions of selective precipitation major part of cobalt by sodium hydroxide from the obtained solution are defined, thus more than 95% of manganese are remained in the solution. The cobalt precipitate is directed to the basic technology and the solution is purified by sorption. The most effective sorbents are chosen, optimum modes of its use are found. Examples of manganese recovery from the purified solutions as MnO2, MnCO3, Mn(OH)2 with a ratio manganese : impurities more than 3000 are presented.In the processes of hard alloys manufacture and processing of cobalt-bearing primary raw materials various cobalt-manganous slimes are formed. After leaching by solutions of mineral acids the problem of cobalt and manganese separation becomes an actual. The common way of metals separation in a solution is the Shreyber’ alkaline method allowing rather selectively to precipitate of cobalt hydroxide by sodium hydroxide. However this way does not allow separating completely target metals because of transfer of some manganese in the hydrated precipitate, even at its rather low content.In the given work the results of researches to improvement of a traditional way by inclusion to hydrometallurgical technology of operation of sorption separation of the specified metals are presented. The main goal is definition of conditions to achievement of the complete removing cobalt at hydrolysis with the minimum sedimentation of manganese and the subsequent additional recovery of cobalt by ionites from the obtained solutions."

Jan 1, 2008

By Amanda C. Lima, Luiz Augusto H. Terrones, Sergio N. Monteiro

"Fabric from weaved yarns made of jute fibers have been considered as reinforcement for polymeric composites. In particular, these fabrics obtained from discarded sackcloth are presently being investigated as environmentally friendly composites with recycled polyethylene matrix. The objective of the present work was to compare the practical properties and economical aspects of these composites with those of conventional materials such as wooden board and gypsum panels for building application. The comparison showed that, depending on the amount of post-used jute fabric, a cost/benefit analysis favors these composites over the conventional materials.IntroductionThe increasing amount of wastes generated by human activities is becoming a worldwide problem of pollution with growing consequences to the environment. The question on how to dispose these wastes is, therefore, a major global issue. Among the possibilities of it gating the problem, the use of materials with characteristics of being renewable, biodegradable and recyclable is considered an environmentally correct solution. Examples of this type of materials are left over lignocellulosic fiber from coconut husks and sugarcane bagasse [1] that, after the primary extraction of edible pulp and juices, can be recover for industrial application. Nowadays, the main use of these fibers is to reinforce polymeric composites applied as components for building construction and automobile parts [2,3]. In addition to these applications, composites reinforced with residual lignocellulosic fibers may replace conventional furniture and panels made of wood and thus help to reduce deforestation [4].Environmental protection is not the only motivation for recycling natural fiber wastes. In developing regions activities associate with collecting and processing residual fibers provide job opportunities for low-income people. Moreover, if the lignocellulosic fiber is collected as a recyclable waste, it hes the economic advantage of a comparatively cost, which constitutes in a relevant difference as a choice for commercial utilization."

Jan 1, 2008

By M. Vijayalakshmi, S. Saroja, C. Sudha, T. N. Prasanthi

"Ti-5Ta-2Nb alloy and 304L austenitic stainless steel were joined by explosive cladding process. Investigations on 'as received' explosive clad revealed high hardness very near the interface due to martensitic transformation of 304L steel base plate. To improve ductility, explosive clads were heat treated in the temperature range of 823 to 1073 K for 1 to 20 h. Consequent change in the microstructure and microchemistry of the clad interface was studied. No change in the interface microstructure was observed for heat treatment at 823 K. Increase in temperature lead to the formation of various reaction zones at the interface, their number and width increase with temperature and time of thermal exposure. Growth kinetics of the reaction zones was monitored and activation energy required for formation was calculated. From elemental redistribution profiles, effective inter-diffusivities of alloying elements were calculated as a function of concentration and activation energy required for inter-diffusion was evaluated.IntroductionFor engineering components exposed to highly oxidizing and corrosive environments, a titanium based alloy i.e Ti-5Ta-2Nb (Ti-Ta-Nb) is often chosen as a structural material [1,2]. For economic consideration, vessels and piping exposed to non-oxidizing conditions are fabricated from 304L austenitic stainless steel (304L SS). Hence, dissimilar joint of Ti-5Ta-2Nb alloy and austenitic stainless steel becomes unavoidable. Fusion welding processes are not suitable for joining Ti and Fe based alloys due to the propensity for the formation of intermetallic phases and subsequent reduction in the bond strength [3,4]. Hence, explosive cladding, a solid state welding technique, was used to achieve high integrity, corrosion resistant joints between the two alloys."

Jan 1, 2012

By James C. Sever

"With the advent of high energy costs and increasing concern for the environment leading to the incorporation the C02 life cycle as a criteria for the material used in a finished product, it is beneficial to analyze the plant and the process used in producing a raw material in order to identify practical, economic energy recovery opportunities. To this end a study was made of the proposed Nevada Clean Magnesium, Inc. Tami-Mosi reduction facility. Each source of waste heat is listed together with the assessment for potential co generation or direct recovery. The overall impact on energy requirement and C02 generation is provided.IntroductionHistorically metal reduction plants, large consumers of energy, do not recover waste heat. This occurred for many reasons:• Energy costs were low and the capital for a co-generation system could not be justified;• Waste heat sources contained entrained solids or liquids which would inhibit efficient energy recovery;• The exit temperature for the heat source was too low for efficient use by aaqueous Rankine cycle system.The business environment has now changed adding impetus to the recovery of energy previously discarded. Power costs have greatly increased. Global warming and the impact of carbon dioxide on the environment has become an issue which could impact the permitting of a plant. Technology improvements especially the development of a scaling environment waste heat boiler [l] and the development of the organic cycle Rankine cycle recovery system enable up to 70% energy recovery from ""low grade"" heat sources [2].With the inception of Nevada Clean Magnesium, Inc. 's (formerly Molycor Gold Corporation, Inc.)Northern Nevada Tami-Mosi project [3], an opportunity was presented to incorporate energy optimization from the initial design phase."

Jan 1, 2013

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 Majid Sarkari, Hossein Atashi, Farhad Fazlollahi

"The aim of this research work was to prepare the efficient catalyst to purify pollutant output gases such as SO2 , NO2 and CO. This catalyst, lanthanum cobaltat (LaCo03) was prepared by the proper method in the analysis laboratory of Tabriz Oil .The first materials were chosen through calcination operation and temperatures of operation related to the Tamman temperature, therefore the basis for the first material of catalyst was nitrate and aqueous and since we had no availability to lanthanum nitrate, lanthanum oxide was used to prepare the nitrate one. Before all else, the first materials of catalyst were mixed together with the equal mole proportions and then, at the lower and upper temperatures of Tanunan temperature, calcination operation was carried out. To determine the molecular structure, the XRD analysis was utilized and specified that prepared lanthanum cobaltat was sixth aqueous and had the crystal structure type Triclinic.IntroductionLaCo03 has presented a vast interest because of its special electrical, magnetic and catalytic properties [1-4]. The catalyst LaCo03 can be prepared by means of several methods such as spray drying, freeze drying and also co-precipitation [5-12]. Some methods including hydrothermal, sol gel and citrate [13] This material usually has been synthesized by ceramic method and certainly the high temperature for the calcination operation. [14]. Lanthanum catalysts have been researched because of having such an active state [15]. One of the unique properties of this catalyst is the simultaneous conversion of pollutant elements. Nowadays CO oxidation has important applications in environment protection, such as indoor air cleaning and automotive exhaust treatment. LaCoO3 is one of the most important catalysts for CO oxidation."

Jan 1, 2013

By Shaohua Ju, Jin-hui Peng, Ya-jian Wang, Shuai-dan Lu, Li-bo Zhang, Lei Guo

"The granulation of a red mud is of great importance for recycling this material as an adsorbent for waste water or gas. A new granulating process was developed and its effect was evaluated. To reduce the cost of the granulation process, the wet filter cake (containing 25% water) was directly mixed with different cement contents (4%, 6%, 8% and 10% based on wet material). The mixtures were placed in a moist environment for 4 days, and then were washed with deionized water until the pH values of leachants were lower than 9.0. The efflorescence ratio, surface area and particle size of the aged mixture were determined, respectively, by bottle shaking experiments, N2 adsorption and screening. The results showed that the best addition of cement is 2%, and this yielded granulated material with a particle size of less than 2 mm, an efflorescence ratio of 4.83% and a specific surface area of 17.42 m2/g.IntroductionRed mud is a residue of the aluminium industry that is produced during the alkaline extraction of alumina from bauxite by the Bayer process. For every ton of alumina that is produced, the amount of red mud generated can vary from 0.3 to 2.5 tons, depending on the characteristics of the bauxite. In its typical form, red mud is brick red in colour, caustic, about three times as dense as water and, when un-neutralised, has a high pH, typically around pH 13 [1]. It is primarily composed of iron oxide, silica and alumina, along with traces of heavy metals. Red mud particles are quite small; typically 99% will pass through a 0.6 mm sieve and 87% through a 0.038 mm sieve [2],"

Jan 1, 2012

By Jorge Alberto Soares Tenório, Denise Crocce Romano Espinosa, Luciana Harue Yamane

"The present work investigated the influence of Fe+2 initial concentrations in the bioleaching of copper from printed circuit board using Acidithiobacillus ferrooxidans-LR. Printed circuit boards were collected from obsolete computers and mechanically processed through size reduction followed by magnetic separation. The bacteria Acidithiobacillus ferrooxidans-LR were grown and adapted in presence of printed circuit boards. A shake flask study was carried out on the printed circuit boards samples (non-magnetic fraction) using a rotary shaker under the following fixed conditions (185 rpm, 30°C). The bioleaching efficiency was evaluated by comparison between the concentration in the initial sample and in the leached liquor, pH of the medium and concentration of ferrous iron produced. Inductively coupled plasma optical emission spectrometry (1CP-OES) was used to determine the metals concentration. The results showed that Acidithiobacillus ferrooxidans-LR leached 63% copper from printed circuit boards using supplemented medium with Fe+2.IntroductionThe waste of electric and electronic equipment is generated by discarding of equipment such as obsolete computers and cell phones which is stimulated by the technology innovations and it has been growing each year. Because of the amount that has been accumulated it has become a prominent environmental problem but also can be a source of valuable materials, such precious and base metals [1,2] The printed circuit boards are found in almost all electric and electronic equipment being composed of polymers, ceramics and metals and can be an alternative source to recover base and precious metals. The precious metals are used in the printed circuit boards to protect against oxidation and base metals because of its conducting properties [3]. The heterogeneous composition of printed circuit board is a limiting factor in the recycling processes and the metals concentrations also range."

Jan 1, 2011

By N. R. Green, N. J. Humphreys, D. McBride, T. N. Croft, M. Cross, D. M. Shevchenko

"Centrifugal casting offers a route to high quality products in difficult to cast high temperature low superheat alloys and thin section molds. Under centrifugal forces metal is forced into thin sections and can fill thicknesses of less than a millimeter. However, due to the high liquid metal velocities there is a high risk of surface turbulent flow and air entrainment within the liquid metal. The combination of interacting flow-thermal-solidification phenomena and associated defects is a challenging modeling task which the authors have previously described and validated. Capturing the metal-air interface, on what are inevitably complex three dimensional geometries, results in highly computationally expensive simulations and simulating a single cast can take weeks on a single processor. This contribution reports on modeling a complex centrifugal cast, gas entrainment, bubble transport and solidification, employing meshes of up to a million elements and investigates the scalability of the model on high performance clusters.Introduction The ultimate goal of any casting procedure is to produce a defect-free product. For difficult to cast alloys, such as Titanium, centrifugal casting has a number of advantage over conventional gravity methods [1]. In the casting of thin sections, such as turbine blades, the metal is forced into the thin sections under centrifugal forces. The centrifugal force can overcome the backpressure due to surface tension and the metal can fill mould sections with thicknesses substantially less than a millimeter. However, the materials used in these castings [2] tend to be highly reactive and requires low superheat. High liquid metal velocity gives rise to a high risk of free surface turbulent flow and of associated entrainment through free surface turbulence [3] and trapping of gas present in the flow [1]."

Jan 1, 2012

By Dinabandhu Ghosh

The stability diagram of the ternary system Ti-C-O is drawn in the present work for four temperatures, 1473 K, 1573 K, 1673 K and 1873 K, showing the stability fields of TiC, Ti, TiO, Ti2O3 and TiO2. An analysis of the system reveals that it is not possible to produce Ti in a carbon-saturated system; instead, the stable product is TiC. However, Ti can be an equilibrium product in a carbon-unsaturated system at prohibitively low values of pCO and pCO2; for example, at 1873 K, these limiting values are: pCO = 10-6.76 atm and pCO2 = 10-13.36 atm, which, when exceeded, produce TiC and TiO respectively. The magnesiothermic reduction is examined through the stability diagram (log pO2 vs. 1/T) of the system Ti-Mg-O, drawn for a number of pMg values, presenting the pairwise stability fields such as Mg(l) + Ti(s), Mg(v) + Ti(s), MgO(s) + Ti(s), etc. The diagram shows that magnesium reduction of TiO to Ti is possible only at T < 1641 K with pMg = 1 atm and only at T < 1569 K with pMg = 0.5 atm. An experimental scheme for Mg vapor reduction of TiO2 is proposed in which an argon stream is passed over a Mg(liquid) evaporator at temperature T1 (say, 1234 K); the resulting Ar-Mg mixture at 1 atm is subsequently flown over a bed of TiO2 at temperature T2. A thermodynamic analysis establishes that complete reduction to Ti is possible and that the best results are obtained when T1 = T2.

Jan 1, 2006

By José Sancho, Julia Ayala, Purificación García, Begoña Fernández

"A study is carried out to see the adequacy of using flying ashes coming out from a Power Station to eliminate the copper present in waste cyanide waters that are generated in gold mines.Tests were carried out to see how effective the use of ashes taken from two Power Stations could become. Later, the tests are made using ashes coming from Narcea Power Station as this station is near the mine under study.The work is centred on looking for an economically adequate solution to close the waste decanting ponds of the mine. After several tests, a solution is reached through filtration in static layers.IntroductionThe use of coal to adsorb some water-soluble substances has been widely studied [1,2,3,4,] both in the treatment of drinking waters and in determined stages of selective detachment of cyanide gold complexes in cyanide lixiviation processes [5]. Flying ashes sent to the atmosphere by Power Stations as a sub-product of the combustion of this combustible are generally made of more of a 70 % of a vitreous aluminosilicated material and of an active residual material which may be changeable making them potentially useable as adsorbents. Nevertheless, the properties of each kind of ashes depend on the characteristics of the Power Station, of the combustibles being used, of the combustion system, etc.The aim of this work is to demonstrate the adequacy of flying ashes to eliminate the copper present in cyanide waters coming from gold mines either by adsorption or precipitation of the metal. For this study, tests are carried out with Asturian ashes which have a low quantity of lime. The results obtained in the tests demonstrate the effectivity of the method used. To be absolutely concrete, the work is carried out to establish the use of these ashes in the closing of Asturian installations of cyanide lixiviation"

Jan 1, 2008

By J. V. Happ

The investigation reported in this paper was prompted by the belief that vacuum processing of copper mattes could provide significant advancement to present-day copper smelting and converting technology. Specifically, vacuum distillation of copper mattes in a unit such as the R.H. vessel used in vacuum degassing of steel, can lead to improvements in: converter flue-gas-cleaning system, purity of acid (or liquid SO2), aisle hygiene, purity of electrorefined copper and smelter flexibility. In the study conducted, removal of Volatile impurities (arsenic, antimony, bismuth, lead and zinc) from liquid mattes, by vacuum distillation in a laboratory-scale equipment was performed. The conditions investigated covered a temperature range of 1123-1223K, absolute pressure of 6.5-0.5kPa (50 - 3 mm Hg) and with bleed gas consisting either of pure oxygen or argon. Six matte samples (four U.S. and two foreign) were tested. Under the "best" conditions arsenic and antimony were reduced to << 0.01% in the product matte. The removal of bismuth, lead and zinc was variable and appeared to be influenced by the matte composition of the sample. As might be expected, the rates of distillation of the various species were increased at higher temperatures and lower absolute pressures. The influence of a small flow rate of gas (02 or Ar) over the melt did not have a signifi¬cant influence on the extent of impurity removal. The magnetite content of the matte was reduced by up to 30% during vacuum treatment and was favored by a low partial pressure of oxygen over the melt. Substantial amounts of sulfur were also evaporated and an, overall increase in copper grade of the matte was realized. The paper concludes with an evaluation of industrial aspects of the process as applied to conventional smelters.

Jan 1, 1983

By Wilson Acchar, Fernando Barcelos, Luis Carlos Pereira

"Porous ceramics have been extensively investigated as structural materials for flow of fluids in many applications, such as filters for molten metals, water purification and hot gases, thermal protection systems and heat exchangers. This class of material must have two special features: high permeability and mechanical strength. However, these parameters are influenced in different ways by the processing method and the consequent cellular structure. In this work two different types of commercial ceramic filter materials are investigated. Characterization included the evaluation of the strength values as well as the permeability behavior and microstructural analyzes of the surface fracture. The results indicate that the strength values are strong dependent on the filament defects.IntroductionCeramic materials with a cellular structure have been extensively investigated as structural materials for flow of fluids applications [1-3]. Microstructural aspects such as morphology, size of the cell and the degree of interconnectedness are mainly parameters that influence the properties of these porous materials [4-6]. The most used industrial process to produce cellular ceramics for filter application is the polymeric sponge replication method. This technique consists in dipping the polymer foam into slurry containing an appropriate binder and the necessary ceramic materials, followed by a heating treatment [2,5].Mechanical properties of cellular ceramics depend basically on cell size, degree of interconnectedness and density [1,2,5,8,9]. Materials used as filters required a good strength and also permeability values. These properties are inversely proportional to each other. Higher porosity increases permeability values but decreases the strength values [1,2,5]. The objective of this work is to study the strength resistance of a commercial porous ceramic material (10, 20 and 30 ppi) based on silicon carbide."

Jan 1, 2012

By G. P. Chaudhari, F. Warchomicka, M. Dikovits, V. Pancholi, C. Poletti

"The hot formability of a microalloyed steel with 0.16 wt-%C modified with N is studied by using processing maps. Compression tests of cylindrical samples are carried out using a Gleeble®3800 simulator in the range of temperature between 750 -1000°C and strain rates between 0.01-100 S-1. For this alloy, an Ar3-temperature about 740°C is determined by means of dilatometry. Processing maps are calculated using the modified dynamic material model developed by Murty and Rao for different logarithmic strains. For the instability map, the parameter Kj developed by the authors in previous works is used and compared with other instability values. Softening in the flow curves provoked by induced ferrite during deformation at low temperatures and low strain rates is reflected in the n-value. Light optical microscopy (LOM) and electron back scattered diffraction (EBSD) measurements are used to study the microstructure of the hot deformed samples to determine the deformation mechanisms active and to verify the processing maps.IntroductionProcessing maps offer a good possibility to optimize thermomechanical process parameters and to avoid defects in the products. Prasad et al. [1] developed the processing maps using the dynamic material model (DMM) and Murty & Rao [2] modified it. Processing maps consist of two superimposed maps: the dissipation efficiency and the instability map. The processing maps can be used to detect areas with a good hot formability, which are normally related to restoration of the material by dynamic recovery/recrystallization. For a high dissipation efficiency value and no instabilities, a good hot formability is predicted. In the DMM no storage of energy takes place and so the material is considered essentially dissipative, this is only true for high temperatures and high strain rates [1]."

Jan 1, 2012

By Chenhui Liu, Ka-ma Huang, Hong-ying Xia, Bingguo Liu, Hua Chen, Jinhui Peng, Libo Zhang

"The rising popularity of microwave heating in mineral processing has fuelled the need for knowledge concerning dielectric properties of minerals. Dielectric property and microwave absorption property of anthracite were measured over a temperature range of 20-100°C at 2.45GHz by using an open-ended coaxial sensor measurement system. The results show that the dielectric constant, loss factor and loss tangent increase with temperature rising at 2.45GHz. Microwave absorption properties of anthracite are highly dependent on temperature and frequency. At frequency of 2.45GHz frequency used in microwave metallurgy, anthracite is suitable for reducing agent to achieve fast elevation of temperature then returning to original state. The research will be helpful in explaining the thermal running of microwave dielectric heating the anthracite.IntroductionThe application of microwave heating in minerals processing and treatment has recently attracted great interest from the metallurgical industry. Compared with conventional heating methods, the advantages of microwave heating include rapid and selective heating, uniform distribution, high efficiency, fast on and off switching as well as flexible and modular design[l-3]. As a result of these advantages, microwave heating has been applied in a variety of mineral processing and extractive metallurgy, such as microwave-assisted ore grinding, microwave heating for carbothermic reduction and acid leaching of ilmenite ore, microwave drying, microwave-assisted roasting and smelting of sulfide concentrate, microwave-assisted spent carbon regeneration and microwave-assisted waste management [ 4-6]. Though the application of microwave heating in the metallurgical industry is promising, further studies on the interaction between microwave radiation and minerals and its effects are highly desired to develop innovative techniques for minerals processing and ore treatment using microwave heating [7]."

Jan 1, 2013

By Donghai Li, Cheng Pan, Xuyang Liu, Xuewei Lv, Chenguang Bai

"Fine chromite ore is the common raw material to produce ferrochrome alloy through the submerged electric furnace process. The electric resistivity of fine chromite ore plays an important role in the operation efficiency because it determines the current distribution. The effect of particle size and the contact area of the particles on electric resistivity for several of chromite were investigated at room temperature, and the relationship between the electric resistivity of mixed particles and the volume fraction of lump ore to fine ore was also studied. The results shown that the electric resistivity increases with the increase of particle size, and the electric resistivity of mixture decreases with the increase of volume ratio of fine ore.IntroductionChromium is one of the most important alloying elements in manufacturing of stainless steel that used at high temperature and corrosive environment applications [I, 2]. As the raw materials to be charged into the steel, ferrochromium alloys and charge chromium are produced directly by smelting of chromite ore with the reducing agent in submerged electric arc furnace (SAF). During the process, the oxides of chromium and iron were reduced by carbon and meanwhile the electrical energy were consumed [3,4]. The ideal industrial process is to achieve high recovery level of Cr and Fe with minimal power consumption. In SAF process, the electric resistivity of charge stock has significant effect on the current distribution, which determines the heat distribution, molten bath structure and chemical reactions in the furnace. High resistance of the charge is desired to reduce the current distribution through the charge stock, thus the electrodes may insert into the charge stock with proper depth to form a high temperature arc heat source, and proper smelting can be realized[5]."

Jan 1, 2012

By Samir N. Shoukry, Mourad Y. Riad, Gergis W. William

"Setting of concrete material is defined as the transitional period between states of true fluidity and true rigidity. Initial and final setting times are measured in the laboratory on the mortar sieved from the mix in a controlled environment where temperature and moisture values are constant. On the other hand, field applications are held in outdoor environments where environmental variations have direct impact on setting time values. In this study, initial setting time of class K concrete, usually used for bridge decks and concrete pavements, are investigated highlighting discrepancies between laboratory and field measurements. 72 mixes have been cast in variable environments and collected data from concrete mixes and the ambient conditions are reported. In light of the collected data, the effects of variable setting times on early age cracking of concrete material are studied and means to minimize such cracks are presented.BackgroundSetting of concrete material is defined as the transitional period between states of true fluidity and true rigidity [1]. Continuous hydration of the cement within the matrix transfers the mix from a state of setting to hardening. Initial and final Setting times are measured in a laboratory setting following ASTM C 403 specifications. Initial setting approximates the time at which the cement paste can no longer be plastic under compaction (or can be handled in a proper fashion), while the final setting approximates the time at which hardening occurs. The standard test described in ASTM C 403 is conducted on the mortar sieved from the mix (paste passing from 4.75 mm sieve opening). Initial and final settings are described as the elapsed time after the initial contact of water and cement till the mortar reaches a penetration resistances of 3.5 MPa (500 psi), and 27.6 MPa (4000 psi) respectively."

Jan 1, 2012

By D. Kennis

"Union Miniere Precious Metal's (UMPM's) Hoboken Business Unit has a long tradition in complex Pb-Cu metallurgy, focussing on the recovery of precious metals from various types of secondary and recyclable materials. Although the old flow sheet, based on a traditional sinter plant, blast furnace, and lead refinery process was a very complete flow-sheet with the capability of dealing with almost every impurity, the weaknesses became clear:1. old and costly technology,2. too many unit operations,3. too much internal recycling, and4. dependency on concentrates for the sintering process.To maintain the competitiveness of the Hoboken Business Unit, the project ""Smelter 2000"" was born. This project represents a breakthrough in metallurgical processes and technology. A modem smelting technology was chosen together with the development of a new process. A lead-copper process combining lead slag and blister copper production, carried out in an ISASMEL T vessel, was the key to simplifying the Hoboken flowsheet. ISASMEL T smelting technology was chosen for its flexibility towards feed characteristics and process parameters.The new smelter was commissioned at the end of 1997. Although there were a lot of problems due to the high degree of technical innovations in the process, the new smelter came to design capacity within 1 year after start-up. During this period, however, UMPM had, a very difficult time because of the extreme clear-cut nature of going from the old to the new flowsheet.After two and a half years of operation, the new flowsheet has proven to fit with the strategy of UMPM, focussing on treating secondary Pb-Cu materials and a broad range of recyclable feeds such as electronic scrap (E-scrap) and catalysts. Together with the new Precious Metals Plant, efficient logistics, recognised world class sampling practices and a customer-focussed commercial organisation, UMPM Hoboken can definitely be considered reborn."

Jan 1, 2000