Search Documents

By Wankun Wang, Shixing Wang, Jinhui Peng, Zebiao Zhang

"Germanium leaching from germanium dust and fume was carried out using sulphuric acid. Response surface methodology (RSM), based on a five level, four variable central composite design (CCD), was employed to obtain the best possible combination of liquid/solid ratio (Xi: 2-10), leaching time (X2: 1-5 h), sulphuric acid concentration (X3:3.15-15.75mol/L) and leaching temperature (X4:50-90 *C) for germanium leaching. The obtained experimental data were fit to a one-order polynomial equation using multiple regression analysis and also analyzed by analysis of variance (ANOVA). The 3-D response surface plot and the contour plot derived from the mathematical models were applied to determine the optimal conditions. The optimum extraction conditions were: liquid/solid ratio of 10, leaching time of 1 h, sulphuric acid concentration of 15.75 mol/L, and leaching temperature of 87.8 'C. Under these conditions, the germanium leaching extent was 65.14%, which is in close agreement with the value predicted by the model. The samples were characterized before and after leaching using X-ray diffraction (XRD).IntroductionResponse surface methodology (RSM) is one of the relevant multivariate techniques which can deal with multivariant experimental design strategy, statistical modeling and process optimization [1-15]. It is used to examine the relationship between one or more response variables and a set of quantitative experimental variables or factors. This method is often employed after the vital controllable factors are identified. It is also used to find the factor settings that optimize the response. Designs of this type are usually chosen when a curvature in the response surface is suspected [6], The process optimization of the sulphuric acid leaching of germanium from germanium dust and fume has not been reported in the literature. Hence the present work intends to assess the effects of variables such as liquid/solid ratio, leaching time, sulphuric acid concentration and leaching temperature and to identify the optimum conditions using RSM. The characteristics of sample before and after leaching are assessed using the advanced analytical instruments such as X-ray diffraction (XRD)."

Jan 1, 2012

By Yasuhiro Konishi, Yoshiyuki Noda

"This paper describes a new processing of rare-earth oxide precursor, in which rare-earth carbonate powders are precipitated directly from emulsions of rare-earth loaded carboxylate solutions, using CO2 gas and water. This synthetic route of rare earth carbonate is a combined process of the stripping and precipitation stages in a conventional solvent extraction. Using this technique, lanthanum carbonate and yttrium carbonate were prepared at temperatures of 10 to 80°C and CO2 pressures of 0.1 to 3.0 MPa for 120 min. The rates of carbonate precipitation in a batch autoclave were sensitive to processing parameters such as CO2 pressure, temperature, and organic-phase composition. The particle size distributions of the carbonate powders were markedly dependent on temperature and C02 pressure.IntroductionSolvent extraction is the most appropriate commercial technology for separation and purification of rare earths. In typical commercial processes, the rare earths are stripped from loaded solvent extractants using aqueous solutions of mineral acid. After adjusting the pH of the aqueous strip solution, the rare earths are precipitated as insoluble powders of oxalates or carbonates, from which oxides can be produced by calcination. Such conventional processing can be simplified when the stripping and precipitation stages are combined by emulsifying rare-earth loaded solvent extractant with aqueous oxalic acid solution. It is likely that the single-stage precipitation stripping results in a marked decline in the consumed amounts of precipitating and neutralizing agents, thereby saving on both running and capital costs.Yoon and Doyle1) first demonstrated that oxalate powders of lanthanum and yttrium are directly precipitated from rare-earth loaded carboxylic acid solvent extractant when contacted with aqueous oxalic acid solution at ambient temperature and atmospheric pressure. Yttrium oxalate pow4ers were also prepared by precipitation stripping of di-(2 ethylhexyl) phosphoric acid. (D2EHPA) extractant using oxalic acid-hydrochloric acid solutions. 2) Moreover, neodymium oxalates were directly precipitated from organic solutions of tertiary aliphatic monocarboxylic acid and 2-ethylhexyl phosphonic acid mono-2- ethylhexyl ester using aqueous oxalic acid solutions, and powder characteristics of the resulting oxalates were compared with those of powders by the conventional solvent extraction routes. 3 • 4) Recently, attention has been directed towards the influence of processing parameters on the particle size distributions of yttrium oxalate precipitates. 5)"

Jan 1, 2000

By G. Johnston, J. Greenly, R. G. Buchheit, D. C. McIntyre, R. Muenchausen, D. J. Rej, R W. Stinnett

"Rapid thermal treatment of materials using high energy, high flux, pulsed ion beams can produce modified surface layers with unique microstrutures and properties. High energy ions loose their energy during the slowing down process in the workpiece and thus deposit their energy continuously over a depth of a few microns. The deposition of energy can lead to melting and in some causes ablation of the heated layer. Because the pulse duration of the ion beams is typically only 50-200 ns, steep thermal gradients generated during heating facilitate rapid cooling (107K/sec-108K/sec) of the treated layer by thermal diffusion into the underlying material. Rapid heating and cooling of materials can generate surface layers with non-equilibrium amorphous or nano-crystalline microstructures that exhibit increased hardness, wear resistance, and corrosion resistance. Pulsed ion beam treatment can also lead to surface smoothening or can be used to mix thin « 1 11m thick) coatings into underlying substrates. Pulsed ion beams can be generated using existing ""flashover"" ion source technology which is capable of producing single shot, mixed C, H, and O ion beams with beam cross sections of approximately 100 cm2 and energy fluxes up to 100 J/ cm2. Recent advances in repetitive high energy pulsed power technology and development of magnetically confined anode plasma ion sources have facilitated the development of ion beam systems that generate single species beams that pulse continuously at 120 shots/second. These capabilities will allow rapid treatment of large surface area workpieces at low cost.IntroductionThe rapid solidification of liquid materials can create unique materials and material microstructures that often have properties that can lead to enhanced performance. Rapid solidification processing of the surfaces of materials using continuous and pulsed laser beams (laser glazing) has been explored for over 20 years (1-5). Advances in high energy, pulsed electron and ion beam technologies over the past decade have provided rapid thermal treatment techniques that may be less expensive to impliment than laser surface treatment for many surface modification applications (6). High energy pulsed ion beams have recently been used to harden aluminum(7), copper(8) and tool steel surfaces (6,9), increase corrosion resistance of Al alloys (6), mix coatings into underlying substrates (10), and create amorphous films (11,12)."

Jan 1, 1994

By Jincheng Hu, Honggang Zhong, Qijie Zhai, Congsen Wu, Cheng Zhang, Jingzheng Ye

"The influence of cooling intensity on the solidification structure and ferrite phase content of a new duplex stainless steel (DSS) was investigated by using a thermal simulation setup for continuous casting. The results showed that the characteristics of the solidification structure were similar to their industrial scale manufactured slabs, including chill zone, colunmar zone and equiaxed zone. And austenite morphologies were mainly primary and secondary Widmanstatten sideplates as well as intragranular Widmanstatten plates. In addition, it revealed that the ferrite content increased with an increasing distance from the chill surface and decreased at colunmar to equiaxed transition (CET) position, then the value remained relatively stable at equiaxed zone. Furthermore, the ferrite content presented the same trend with the cooling intensity ranging from 100 mL/min to 2000 mL/min with the values just varying in a slight range.IntroductionThe duplex stainless steel (DSS) is the kind of steel that ferrite phase and austenite phase occupy about 50% respectively, or the content of the fewer phase has to be more than 30% [l]. The success of modem duplex stainless steels is to a large degree due to their higher strength than austenitic stainless steels, higher toughness than ferritic stainless steels, good weldability and high resistance to stress corrosion cracking as well [2,3]. The cost of stainless steel production continues to soar in recent years due to the increasingly higher price of Cr. In order to decrease the production cost, a new type of duplex stainless steel was developed by Bao steel [4]. This newly developed duplex stainless steel had low Cr content compared with 2205 DSS, and was expected to be applied into automobile industry. However, this type of steel was still in the initial stage of development, and the influence of continuous casting process on its solidification process and structure was still unclear, which needed to be studied further. Several works published in literature presented the effect of continuous casting conditions on duplex stainless steel (DSS) 2205, 2304 [5,6]. It was discussed that the cooling intensity in the chill-side had little efficient influence on the phase transformation. In this paper, the effect of cooling intensity on the solidification structure and ferrite volume fraction of this DSS at a given cooling rate was investigated."

Jan 1, 2014

By H. Kamiya, H. Hasegawa, M. Nojiri, S. Matsui, Y. Fukuda, M. Tsukada

"The present paper focuses on the action mechanism of anionic polymer dispersants in dense Si3N4 and SiC suspension. An atomic force microscope (AFM) was used to determine the relationship between the macroscopic suspension viscosity and the microscopic adsorbed structure of a polymer dispersant at the solid / liquid interface. The surface interactions within the suspensions were analyzed in various dispersant pH and additive conditions. The addition of an anionic polymer dispersant decreased Si3N4 and SiC suspension viscosity and increased electro-steric repulsion force on the non-oxide surface in solution at pH> 6 which was the isoelectric point of the materials. It was assumed that the increase of repulsive force was promoted by a hydrophobic adsorption of polymer dispersant on the non-oxide particles.IntroductionThe surface of silicon nitride and silicon carbide powders in a water suspension system has quite a complex molecular structure. In the case of Si3N4, hydroxyl and ammonium groups form on the surface and the pH of the suspension is increased from neutral to about 10 due to surface oxidation. The particle surface is negatively charged in alkaline solutions (pH=10), because the isoelectric point of silicon nitride exists in the pH range from 5 to 6. However, in spite of charging the negative surface charge, an anionic polymeric dispersant is generally used for the reduction in slurry viscosity.In dense SiC suspensions, an anionic polymer dispersant is generally used in order to disperse aggregates and reduce the suspension viscosity, too. Since an anionic dispersant is used in alkaline solutions higher than the isoelectric point of silicon carbide, the dispersant adsorbed on the negative charged surfaces of SiC.Few researchers have discussed and estimated the adsorption mechanism and structure of anionic polymeric dispersants on silicon nitride and silicon carbide surfaces. This is because it is difficult to observe the structure and measure the interaction at the solid/liquid interfuce directly. However, new developments in surface-force measurement technology have enabled the determination of non-DLVO type interaction for analyzing aggregation behavior2. The use of the AFM for analyzing the effects of various surfactants and co-polymers on colloidal dispersions and solid surfaces has also begun to rapidly expand to characterize the interaction between solid surfaces."

Jan 1, 2000

By Suman Das, Justin J. Gambone, Rohan Bansal, Ranadip Acharya, Paul Cilino

"This paper focuses on generating a quantitative microstructure prediction model for Scanning Laser Epitaxy (SLE) process based on coupled flow-thermal modeling using Finite Volume method. SLE is a laser-based additive manufacturing process for the deposition of equiaxed, directionally solidified and single-crystal nickel superalloys through the melting of alloy powders onto superalloy substrates. In the current work, the detailed effects of natural and Marangoni convection on the flow field are studied and the results are analyzed in terms of the temperature gradient, vorticity parameter, melt pool dimensions and mushy region extent. The detailed property data of the processed superalloy and the laser scan path are incorporated in the model to predict the microstructure in realistic scenario. An optimization study is carried out to evaluate the critical parameter values at which the columnar-to-equiaxed and the oriented-tomisoriented transition take place. This work is sponsored by the Office of Naval Research through grant N00014-11-1-0670.IntroductionSLE is a laser-based additive manufacturing process for the creation of structures in equiaxed, directionally solidified and single-crystal nickel superalloys through the selective melting and resolidification of superalloy powders. In SLE, a tightly focused laser beam is guided by a highspeed galvanometer scanners allowing for tight control of the amount of energy being applied to the top of the powder bed, as well as the speed at which the melt pool moves across the substrate. Under the proper operating conditions and with sufficient substrate meltback, the solidification microstructure follows the morphology of the underlying substrate, allowing for directional and even SX growth.Several reports on the modeling aspects of laser cladding-based additive manufacturing approaches can be found in the literature. Approaches based on Finite Element Methods (FEM) and Finite Volume Methods (FVM) are employed for the thermal modeling of the system [1, 2]. Gaumann coupled the Columnar to Equiaxed Transition (CET) modeling with the Rosenthal solution in earlier work based on laser cladding [3]. Rappaz et. al. provided a detailed modeling of the microstructure/columnar orientation based on the solidification velocity and crystalline orientation [4]. This approach is based on the selection of the growth direction that closely follows the melt pool normal direction. Later on, substrate orientation is also taken into account [5, 6]."

Jan 1, 2013

By Brommerm Tracey, Britt Elin Gihleengen, Elsa Olivetti, Hans Ole Riddervold, Randolph Kirchain, Geir Øyen

"Compositional uncertainty in secondary materials and variable processing conditions inhibits secondary material utilization in the production of aluminum alloys. Efforts to implement optimization models that direct batch planning have limited industrial presence due to factors such as the insensitivity of these optimization models to dynamic plant circumstances. This paper describes a chance constrained model formulation that generates lower cost, robust batch plans with significant flexibility towards changes in processing conditions. The principal attribute of the chance constrained formulation is its inherent mitigation of risk by diversifying the batch plan. This paper compares aluminum remelter batch planning using the chance constrained formulation with a traditional deterministic model and a manual batch planner. With the expectation that volatile material prices, restricted scrap material availability, and pressure by consumers and legislation for increased recycled raw material input will continue in the future, batch planning tools that inherently diversify a production portfolio will become increasingly advantageous for industrial aluminum remelters.IntroductionAluminum remelters must develop strategies to incorporate lower cost secondary materials into finished alloys to remain competitive amidst increasingly demanding market and regulatory conditions. Determining the optimal combination of incoming raw materials to produce an alloy that meets compositional specifications presents remelters with a complex problem that has driven the development of computational tools commonly referred to as batch planning or blending algorithms. The ubiquity of the ingredient or raw material blending problem in production has motivated ongoing development of batch planning algorithms since the classic nut-mix problem in the 1950's [1]. The most common model formulation for industrial aluminum remelters are deterministic, linear optimization programs [2]. These blending problems determine the optimal combination of raw materials by minimizing cost subject to constraints around demand, availability, and compositional specification. Despite extensive research and moderate computational requirements, batch planning algorithms are inconsistently used in industry. Insufficient incorporation of the complexity of real world remelting conditions into these models provides an obstacle for their implementation [3]. For example, many batch planning algorithms do not explicitly incorporate the impact of compositional variation of the raw materials on overall batch cost. Additionally, they do not allow for endogenous specification of tolerance to error in batch planning, so provide little flexibility where a batch planner would like to incorporate materials of greater uncertainty. Incomplete accounting for quality variability undervalues secondary materials leading to overly conservative use [ 4, 5]."

Jan 1, 2011

By Xue Wang, Callie Babbitt, Chelsea Bailey, Matt Ganter, Gabrielle Gaustad, Brian Landi

"Current trends, motivated by fossil fuel dependence and unprecedented greenhouse gas (GHG) emissions, show lithium-ion batteries (LIBs) emerging as a competitive energy storage technology due to higher power and energy densities compared to Pb-acid and Ni-metal hydride chemistries. These trends may be of concern, however, as environmental impacts are not well understood for either the LIB itself, or for the nanoparticles consumed or released during the battery's production, use, or end-of-life. This study combines economic modeling, dynamic material flow analysis, and fundamental material characterization methods in order to quantify some of the economic and environmental trade-offs for LIBs at their end-of-life. As expected, results show that as chemistries transition from Li-Co based cathodes to Li based Fe, Mn, and S cathodes, LIB recovery value correlates to the value of the raw materials used. These initial results aim to inform collection policies being proposed currently as well as enable future deployment of novel recycling techniques.IntroductionGlobal fossil fuel dependence and unprecedented GHG emissions have led to increasing attention on energy alternatives, for both electricity production and personal transportation. However, development of renewable energy systems is contingent on concurrent technological development of energy storage systems, primarily batteries used for power grid load-leveling, renewable energy storage, and hybrid and battery electric vehicles. In this sector, lithium-ion batteries (LIBs) are emerging as a competitive technology due to higher power and energy densities compared to lead-acid and nickelmetal hydride chemistries[!]. LIBs represent close to 20% of the total rechargeable battery market and 75% of the portable rechargeable battery market, which is the fastest growing segment of the rechargeable battery market, with a 20% global growth in 2008 [2].This surge in production ofLIBs indicates a looming waste problem; total waste from Li-ion batteries has likely grown substantially from the 500 metric tons estimated in 2003 [3]. Figure IA shows the substantial increase in world-wide lithium production that has occurred in the last several decades with batteries making up the largest share of applications (Figure lB). California and New York state legislators have attempted to proactively address this looming waste by issuing diposal bans on rechargeable batteries in their states[4, 5]. However, quantification of the costs involved in collection, transportation, and processing of these materials has not been examined in depth."

Jan 1, 2012

By Teruo Bitoh, Shogo Izumi

"The effect of B203 flux melting on the structure and the soft magnetic properties of the (Feo.1sBo.20Sio.os)96Nb4 bulk metallic glasses prepared by casting has been investigated. The ringshaped bulk specimens were prepared by the B203 flux melting and copper mold casting. It was confirmed that the flux melting promotes the precipitation of the a-Fe(-Si) and Fe2B phases in the central region of the specimens. The ring-shaped bulk specimens show a flat hysteresis curve, indicating a good linear relationship between the magnetic induction and the applied magnetic field. These results show that it is possible to develop a new soft magnetic material that exhibits constant permeability, which is necessary for producing inductors and choke coils.IntroductionSince the success of forming Fe-based bulk metallic glasses (BMGs) with good soft magnetic properties, great attention has been developed to synthesis and properties of the BMGs [l, 2]. The BMGs have high glass-forming ability (GFA) and, therefore, they can be used to prepare bulk amorphous alloys with a thickness of the order of a few millimeters by casting. The soft magnetic properties of Fe-based BMGs are better than those of ordinary amorphous alloys; therefore, these BMGs have wider applications as soft magnetic materials [3-5]. It is often required for soft magnetic materials that the shape of the hysteresis curve is changed according to the demands of applications. For example, materials with ""flat hysteresis curves,"" which means the magnetic flux density (B) and the applied magnetic field (H) show a linear relationship up to rather high magnetic field, are necessary for producing inductors and choke coils. Flat hysteresis curves can be easily achieved by creating an air gap in the magnetic path. However, magnetic flux leakage generated in the air gap inhibits high-density packing of the electronic components. In order to achieve flat hysteresis curves without creating an air gap, Fe-based ordinary amorphous alloys are subjected to crystallization by annealing and transformed into thin surface layers of a-Fe; the crystallization results in the compression of the remained amorphous phase [6]. Another way to achieve flat hysteresis curves is the formation of secondary phase (such as Fe2B) that act as pinning site of magnetic domain wall displacements [7]."

Jan 1, 2013

By Toshiro Kuji, Masakazu Fujita, Tetsuji Saito

"The magnetic properties of the magnetic materials were deeply dependent on the microstructures. In this study, the novel technique to produce the desired microstructures in a controlled manner was proposed. The technique consisted of the production of the amorphous alloys and the control of the crystallization process. The technique was applied to improve the magnetic properties of Nd-Fe-B permanent magnets. The microstructural control of the magnets exhibited the excellently high energy-products of higher than 430 kJm-1. The relationship between the magnetic properties and the microstructures of the Nd-Fe-B permanent magnets was discussed.IntroductionThe intrinsic properties of the materials are basically determined by the properties of the constituent elements or the compounds. However, it is often noticed the difference between the observed properties and the theoretical values expected from the intrinsic properties of the materials. This indicates that the observed properties of the materials are determined not only by the properties of the constituent elements. In other words, the observed properties of the materials are also strongly dependent on the morphology of materials. This means that the microstructural control may creates a great improvement of the properties of materials.In Nd-Fe-B permanent magnets, the superiority arises from the uniaxial intermetallic Nd2Fe14B compound which has a large saturation magnetization and a high anisotropy field [1,2]. The magnetic properties of the Nd-Fe-B permanent magnets are dependent on the microstructure, that is, the size, shape and degree of the crystallographic alignment of the Nd2Fe14B phase. Currently, the Nd-Fe-B permanent magnets have been produced by either sintering or melt-spinning [3,4]. In the sintered magnets, alignment of the Nd2Fe14B phase is achieved by the prior green compaction of the crushed ingot powders in an applied magnetic field [3]. In the melt-spinning approach, alignment of the Nd2Fe14B phase is achieved by hot deformation [5]. Amorphous melt-spun ribbons are comminuted and then are consolidated into bulk form by hot pressing before hot deformation. As-hot-pressed magnets have randomly oriented Nd2Fe1~ grains [6]. Subsequent die upsetting of as-hot-pressed magnets gives rise to the crystallographic alignment of the Nd2Fe14B phase."

Jan 1, 1998

By T. T. Natarajan, Nagy EI-Kaddah

"Numerical simulation of electromagnetic confinement systems generally requires large CPU time due to the strong coupling between the electromagnetic and the free boundary problems. The present paper examines the accuracy and the computational efficiency of the most common numerical schemes used in modeling such systems. Levitation melting was taken as a test case. In this study, a comparison was made between the finite element and surface integral methods for electromagnetic field calculations. The computational efficiency of Lagrange and the modified Hestenes methods for solving the free boundary problem were investigated. The convergence of the Lagrange method was found to be much faster than the modified Hestenes method. It was also found that finite element method not only gives accurate solutions, but faster convergence to the final equilibrium shape than the surface integral method. The applications and the limitations of these techniques in modeling electromagnetic confinement systems will be discussed.IntroductionIn recent years there has been a growing interest in the use of electromagnetic forces for confinement of molten metals as a means to eliminate molten metal contamination during melting and to improve surface quality of cast products. Continuous casting of metal without contact of a mold is now a reality, and is being commercially applied for casting of aluminum slabs /1/, and copper rods /2/. New applications of electromagnetic confinement in melting and casting include containerless melting (Magnetic Suspension Melting) /3/, edge containment in twin roll casting, and meniscus shape control in continuous casting of steel /4/.Modeling of confinement systems involves the determination of the electromagnetic field and the equilibrium shape. These two problems are strongly coupled due to the dependence of the field on the shape of the melt. While significant advances have been made in computational electromagnetics /5/, the application of developed computational techniques to electromagnetic confinement problems is not a simple task. The principal difficulty in using these methods is that the solution domain is not known a priori. due to coupling between the electromagnetic field and the free boundary problems. These two problems have to be solved simultaneously, leading to an iterative solution procedure. As a result, numerical simulation of electromagnetic confinement systems are computationally intensive with computational time at least an order of magnitude larger than the fixed domain problems."

Jan 1, 1994

By Cassandre Nowicki, Louis Gosselin, Carl Duchesne

"Quebec's primary aluminium production industry consumes roughly 39 TWh of electricity per year and is accountable for roughly 7 million tons of CO2 equivalent. By tapping only a small portion of waste heat and integrating it inside the production facility itself, we can significantly reduce GHG emissions and energy consumption. Although the amount of thermal waste can be adequately estimated by applying an energy balance to production processes, this provides very little information on the quality of waste heat and its potential for integration. A measure of exergy is required. Waste heat streams characterized by high exergy content may generally offer valuable incentives for recovery and integration. More generally, exergy values limit integration possibilities. An exergy analysis is provided for the aluminium electrolytic reduction process. This is meant to guide future heat recovery initiatives and energy efficiency measures.IntroductionCanada is one of the world leaders in primary aluminium production and 92% of its aluminium production capacities are located in the province of Quebec. In 2007, production capacity reached 2,786,000 tons in Quebec alone. Since it is estimated that 2.5 equivalent tons ofCO2 are released for each ton of aluminium produced in Canada, Quebec's aluminium production industry is accountable for roughly 7 million tons of CO2 yearly [1, 2]. Furthermore, with an average electricity consumption of 14 MWh per ton, primary aluminium accounts for 39 TWh of electricity per year in Quebec and this energy consumption represents 350 thousand tons ofCO2 equivalent [3, 4]. Natural gas consumption associated with primary aluminium production accounts for less than 1 TWh, but it represents an additional 350 thousand tons of CO2 equivalent [ 4].This work is meant to provide a tool to guide future efforts towards heat recovery and energy efficiency in the primary aluminium industry. Waste heat recovery and thermal integration can cut down both energy consumption costs and GHG emissions. In a primary aluminium production facility, waste heat represents roughly half of the energy input into the Hall-Heroult process. Tapping only a small portion of this energy could reduce natural gas and electricity consumption significantly. In order to evaluate how much of this energy is actually usable, we propose to apply an exergy analysis to individual transformation processes in an aluminium production facility, such that a potential to do work can be assigned to every waste heat flux. The approach will be described in the next section."

Jan 1, 2012

By Zhongliang Tian, Yun Cheng, Yexiang Liu, Ming Jia, Yanqing Lai

"A fundamental electrochemical study of Si ions in Na3AlF6-LiF melts and electrolysis using liquid cathodes was conducted. Cyclic voltammograms (CVs) clearly showed the depolarization of silicon deposition on liquid cathode by forming chemical complexes with the liquid solvent metals. Besides, co-deposition of Al and Si is possible when Si ions are insufficient in the molten salt. Based on the electrochemical results, silicon diffusion into liquid cathode is modelled and evolution of Si activity with concentration is deduced by a mathematic approach. Electrochemical study using liquid metals as working electrodes, can be used as an alternative approach for the acquisition of basic data on alloy behavior. Galvanostatic electrolysis showed that liquid cathodes are appropriate to collect the deposited solid silicon and the highest collection efficiency is almost 85%.IntroductionRecent years have witnessed an increasing demand for solar-grade silicon (Si) by the photovoltaic industry [1-4]. The preparation of high-purity metals through electrolysis and electrorefining offer many advantages such as low cost, low-energy consumption, and environment-friendly process, and thus has been widely used worldwide. From the perspective of electrochemistry [5-7], by utilizing the electronegativity difference between the impurities and Si and controlling the relevant process parameters, it is possible in principle to electrodeposit monatomic Si from a Si4+-containing compound melt. Moreover, because the carbon content of the high-purity Si obtained through electrolysis can be effectively controlled and used as a very ideal raw material in the preparation of electronic-grade and solar-grade Si, the preparation of high-purity Si through electrolysis has received widespread attention [8,9]. Monnier et al. [9] used a graphite electrode to obtain high-purity Si (99.9 %-99.99 %) from Si02/Na3AlF6 system through electrolysis; however, because the Si was precipitated in a solid form and showed poor conductivity, the deposition rate was too slow. Olsen et al. [10] obtained high-purity Si films via electrodeposition in K2SiF6/KF-LiF system by selecting electrode materials with high surface quality (such as Ag and graphite). However, in order to ensure the film quality, the deposition current density must be relatively low (10-50 mA/cm2), resulting in a low current efficiency and low deposition rate, which are not conducive to reducing energy consumption and applying to practical use"

Jan 1, 2014

By Lucas Nana Wiredu Damoah, Lifeng Zhang

"The use of electromagnetic field to remove suspended particles from metals such as aluminum by pushing to the boundary has been well studied. However, the potential of this method is yet to be exploited for the removal of inclusions from silicon. Considering the increasing amount of Top-cut SoG-Si scraps year upon year, there is the need to harness all the potentials of technologies to recycle this materials to ensure sustainability. This study investigates, and discusses new results on the effect of processing parameters such as composition, coil current, and frequency on the removal of inclusions from silicon under high frequency AC electromagnetic field.IntroductionThe solar cell silicon making industry requires pure and clean silicon in order to maximize the conversion potential of the solar cell material. The conversion efficiency of solar cells is limited by minority carrier recombination at dislocations and those intra-granular defects such as impurities, small clusters of atoms, or precipitates [1]. Recent global developments in the energy sector with a drive for the production of clean, reliable, and affordable energy have stirred a rapid growth in the production of photovoltaic (PV) cells.[2] Thus over the years, silicon based PV cells has seen a lot of growth as it has a PV market share of over 90 % [3] either as single-crystalline silicon, or multi-crystalline Si (MC-Si), or amorphous Si [4]. MC-Si produced by directional solidification of solar grade silicon melt dominates the silicon PV market. During the directional solidification process, SiC and Si3N4 particles within the melt are pushed by the solidification front to the top of the ingot which is the last to solidify. Therefore the top of the ingot is cut generating what is known as top-cut solar silicon scraps. The Si3N4 particles are mainly from the coating material at the inside surface of the silica crucible and from the air absorption during solidification process. The SiC particles mainly stem from the carbon reduction process of the primary production of silicon [5]. For sustainability the silicon in the top-cut silicon scraps must be recovered. Therefore methods for removing non-metallic particles, such as SiC and Si3N4, from the silicon are important in order to recycle the top-cut scraps to a useful feedstock for the silicon solar cells manufacturing."

Jan 1, 2012

By S. V. Ketov, V. P. Menushenkov, V. S. Shubakov

"The glass samples were obtained by melting of the oxides mixture SrO-Fe2O3-B2O3(Al2O3) at 1200-1250°C with subsequent quenching of the melt on quickly rotating steel roller. Submicronsized Sr(Fe,Al)12O19 particles were formed in glass-ceramic matrix during the crystallization aging of glass. The aging temperature Tag varied in the range 650-950°C. The submicron-sized hexaferrite powder was obtained by removing of the matrix phases using etching. The samples were characterized by X-ray diffraction, scamiing electron microscopy and magnetization measurements. The glass-ceramic material exhibits very high coercivity value up to 10 kOe. The samples of magnets were obtained by pressing of the hexaferrite powder at RT and subsequent aging in the range 900-1200°C. The aged samples exhibit coercivity value up to 8 kOe.IntroductionStrontium M-type hexaferrites have been widely used in technology and industry mainly for production of permanent magnets owing to their appropriate magnetic properties, chemical stability and low cost [1,2]. The SrFe12019-based compounds are characterized by high magnetocrystalline anisotropy and single easy magnetization axis. The highest coercivity is received for monodomain, defect-free single crystal particles with size D - 100 mn. Finely grained strontium hexaferrite prepared by chemical methods such as sol-gel pyrolysis and oxide glass crystallization exhibits high coercivity up to 6-8 kOe [3-5]. Owing to the partial substitution of Al for Fe in the strontium hexaferrite leading to the increase in the magnetic anisotropy field Ha=2Ki/M,, the increase in the coercivity may be received [6]. The notable results were achieved using the SrO-Fe2O3-AlzO3-B2O3 glass crystallization and formation of perfect submicron crystals of alumina-doped hexaferrite [ 6, 7]. The coercive force of glassceramics reached values of up to 10 kOe. Hexaferrite particles are well faceted and have the shape ofhexagonal bipyramids with truncated vertexes [7].In the present paper, we report results of our investigation into the SrO-Fe2O3-B2O3(Al2O3) glass crystallization, hexaferrite powders and permanent magnets, which were prepared by pressing submicron-sized hexaferrite powders at RT and subsequent sintering at 900-1200°C."

Jan 1, 2012

By Feng Ningchuan, Guo Xueyi, Tian qinghua, Liang Sha

"In this study, copper adsorption by orange peel which was chemically treated with sodium hydroxide was investigated. The morphological and chemical characteristics of the adsorbent were evaluated by spectroscopy and N2-adsorption techniques. Equilibrium isotherms and kinetics were obtained and the effects of solutions pH, adsorbent concentrations and temperature were studied in batch experiments. Equilibrium was well described by Langmuir and Freundlich isotherms and kinetics was found to fit pseudo-second order type adsorptions kinetics. According to the Langmuir equation, the maximum adsorption capacities (qm) for Cu(II) was 50.25 mg·g-1 at pH 5.3. With the temperature increased from 16 to 60°C, copper removal decreased. The loaded adsorbent was regenerated using HCl solution and could be used repeatedly at five cycles with little loss of adsorption capacity. The results show additional chemical treatment of the adsorbent by NaOH, is favor of improving the adsorption capacity. Introduction Increased use of metals and chemicals in manufacture industries has resulted in generation of large quantities of effluent that contains high level of toxic heavy metals and it poses environmental-disposal problems due to its non-degradable, persistence nature and accumulation throughout the food chain [1, 2]. Copper is known to be a commonly used heavy metal. This metal, which found many useful applications in our life, is very harmful if charged into natural water resources and may pose finally a serious health hazard. Many methods, such as chemical precipitation, ion exchange, reverse osmosis and adsorption, etc., have been used for heavy metal ions removal from various aqueous solutions. In recent years, there has been considerable interests in use of biological materials including algae, bacteria, fungi, agricultural by-products and residues as adsorbents to remove toxic metals from aqueous solutions by adsorption [3-8]. Adsorption process has been extensively used to remove copper from aquatic medium using low cost adsorbents such as peanut husks [9], plant materials [10] and cellulose materials [11]. Among them, agricultural by-products and biomass are relatively cheap and show very high adsorption capacities. However, to apply untreated agricultural by-products as adsorbents has the disadvantages such as low adsorption capacity, high chemical oxygen demand (COD) and biological chemical demand (BOD) as well as total organic carbon (TOC), due to the release of soluble organic compounds contained in the plant materials such as lignin, tannin, pectin and cellulose, into the solutions [12-14]."

Jan 1, 2008

By Jiu-ju Cai, Wen-caho Liu, Fei Liu

"With the northern cities of China as study objects, and to confirm Ground-source heat pump system of the environmental benefit and the developing direction. In this paper LCA was applied to the environmental benefit Ground-source heat pump System from raw materials acquisition to system production, utilization and disposal. The conclusion shows that Ground-source heat pump system of the environmental benefit in the northern cities of China. The result showed that Ground-source heat pump system had remarkable environmental benefit. 1. Introduction Life cycle assessment Originate in the sixties of last century, what it paid close attention to is to obtain processing from products raw materials, the processing of products produces, products transportation, products use and maintain to the influence to environment of course. It is a products -oriented environmental management style, it is the environmental management mode of meeting the needs of sustainable development strategy [1]. The research object was in the city and lie in the North of China, would undertake Beijing Olympic Games some football matches in the second half of 08, in order to improve the local environment, adjust the energy structure, reduce the heating consumption of urban coal in the centre, eliminate the coal-burning boiler under 10 tons, since 2005, the local government promotes and utilizes actively the heat pump technology in the source substitute the heating of coal-burning boiler. At present, this area is adopted the technological heating area of heat pump of source reach 20 million square meters, account for this area heat 11.2% of area always, it is estimated, by 2010, adopt the technological heating area of heat pump of source will reach 65 million square meters, the proportion of the area rises to about 30% to account for this area and always heat [2 ]. Study to the whole lifespan of heating system of heat pump of ground source of this area on the basis of LCA method, obtain the products impact on environment of different stages and environmental benefit, find out and reduce or dispel the measure of the influence, improve the environmental benefit of the ground source heat pump heating system.2. MethodologyThe research approach used in this research is the Life cycle assessment, the frame of the research approach is goal and scope definition, the inventory analysis, impact assessment, interpretation.[3][4][5]"

Jan 1, 2008

By Vladimir Lobanov, Vladimir Skorohodov, Boris Radionov, Olga Makovskaya

"The synthetic sorbents and the activated carbons which are used for the metals extraction from weak process liquors are rather expensive. It is propose to use mineral and synthetic high-porous substances which sharply increased sorption properties by special processing. For achievement the desirable properties sorbents are impregnated by specially prepared solutions. Such solutions should contain the substances or its anionic forms which on the one hand are strong enough fixed in a supporter pores, with another are capable to form the insoluble compounds with extracting metals. Selectivity is provided by chemism of the reagent interactions with extracting metal. Due to the high concentration of a reacting ion in a sorbent phase the capacity and rate of sorption increases. Formed insoluble compound remains in a phase of the sorbent and necessity of its filtration disappears. For synthesis the sulfhydryl compounds which chemical properties allow to increase degree of extraction and capacity of the activated carbon were used. At hydrometallurgical processing of precious metals mineral raw materials the commercial solutions with the concentration of gold from 0,1 to 5 mg/dm3 are received. Commonly gold is precipitated from cyanic solutions by the zinc dust. The sorption methods are widely applicable. But the synthetic sorbents and the activated carbon using to these purposes are rather expensive. Expenses for sorbents even at its regeneration can reach 10-15 % from total expenses of gold extraction from ores. When sorbent regeneration, mostly for carbon, is not provided, this share increases to 30-40 %. Thereupon search of the sorbents combining availability, the sufficient capacity, demanded degree of extraction and the low price is actual. For the specified purpose it is offered to use the mineral and synthetic high-porous materials which sorption properties are sharply rose by special treatment. Among such substances are natural zeolites, silica gel, lignine et al. Similar treatment can improve the sorption properties of sorbents used in practice, particularly, the activated carbons. The simplest treatment of potential sorbents consists in its impregnation by specially prepared solutions. Such solutions should contain substances or its anionic forms - impregnating agents. These agents should be on the one hand strong enough fixed in a carrier pores, on the other hand are capable to form with extracting metals insoluble compounds. The more strong compounds are formed the high degree of metals extraction from solutions. The sorbents with similarly changed properties are named the impregnated sorbents."

Jan 1, 2008

By Hai-Xing Fang, Chao Liu, Tao Zhang, Bing Xie, Hong-Yi Li, Cui Li

"Hongge Ore, a kind of vanadium-titanium magnetite ore containing high content of chromium, is valuable resource for extracting Fe, V and Cr in China. During present processing of the ore, vanadium and chromium were both concentrated in slag, leading to higher content of chromium in the vanadium slag than that of common one in Pan-Steel. Mineral phases and characteristics of spine! crystals, which influenced greatly subsequent roasting process, in the vanadium slag under different cooling conditions were investigated by using XRD and SEM/EDS. Results showed that vanadium slags containing various contents of chromium were composed of spine!, in which V and Cr were both concentrated, olivine and pyroxene. Growth rate of spine ls decreased sharply below 1350°C. The non-isothermal crystallization process could be described by modified Avrami equation and Ozawa equation. Avrami exponent and Ozawa index were calculated and growth mechanism of spine! crystals was discussed.IntroductionVanadium (V) as well as chromium (Cr) is important non-ferrous metal widely used in materials and chemical industries [1, 2]. Especially, both of them are important alloying elements for the production of high alloyed steels to achieve desired physical-chemical and mechanical properties. Vanadium-titanium magnetite ore in Panzhihua-Xichang area (China) is an important raw material for extracting vanadium. During the extracting process, vanadium is firstly reduced into hot metal and then concentrated in slag phase by blowing oxygen into the hot metal in converter [3]. This kind of slag containing 5~20 wt% V20 3 are usually roasted with sodium or calcium salts and then leached to obtain vanadium containing solution and final products. Current vanadium slag obtained from normal vanadium-titanium magnetite ore contains low content of Cr20 3 and chromium extraction is thus ignored. However, chromium content in the vanadium slag would be increased intensively when the Hongge Ore used, which is also important vanadium titanium magnetite in Panzhihua-Xichang area containing 0.2~0.8 wt% Cr203. Therefore, this kind of vanadium slag with high content of chromium would also be important sources for vanadium and chromium extraction. According to previous work [4], both vanadium and chromium could be extracted from vanadium slag with high content of chromium by salt roasting and leaching, which is illustrated in Fig.1."

Jan 1, 2013

By Tzu-Chien Lin, Jack Tsai, Ming-Yu Lin, Der-Ray Huang, Jiin-Sen Chen, Jing-Xuan Lin

"In this paper, some DVD-R discs have been selected for long time light exposure test and high temperature and humidity test. Generally, recordable media under long time light exposure maybe be defected seriously. If we use Jitter value 8% as a reference to determine the life time of DVD-R samples, some discs defect after 5 hours of light exposure while some discs can endure over 25 hours. Also if we use reflectivity 45% to determine the life time, some discs defect after 30 hours light exposure while some discs can endure over 40 hours. From our results, the good samples show good characteristics of PI error. The absorption spectrum of recordable media is a good reference to justify the quality of dye media. These results can be used to estimate the life time of recordable discs.IntroductionIn general, the life time of DVD-R with a layer of organic dye recording layer is required for preservation in decades. In addition to optical characteristics and thermal properties, we still need to consider the stability of the dye in recording media. The presentation of the color on organic dye is not only related to the material's property but also related to the light exposure. In this study, we focus on the absorption characteristics and reflectivity of organic dye in optical recording layer after light exposure. The optical properties of discs depend on the functional groups and molecular structure [1]. According to ""DVD Specifications for Recordable Disc (DVD- R)"", the reflectivity should higher than 40%. From measured reflectivity, we can confirm that the important issue is whether dye be affected by light exposure or not. Because each specific functional group absorbs the specific spectrum, we can check the characteristics of functional groups from their UV/Visible Spectra. We also use High-performance liquid chromatography (HPLC) to detect the different components of dye on the recording layer [2]. The jitter value test is to test the error cause by digital signal of recording media. If we use jitter value 8% as a reference to determine the life time of DVD-R samples, the purpose of this study is to investigate the jitter values of recording media after high light exposure and high temperature/humidity test. The results of these test will be helpful for the development of long-life optical storage media."

Jan 1, 2012