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By Kunio Nakahara, Kashiwagim Junichi, Takao Hayashi

"There are many problems for electronic devices and parts which were caused electrostatic damage by static electricity. It is necessary for prevention of electrostatic charge to decrease surface resistivity of material using electroconductive coating. Mitsui Mining & Smelting Co., Ltd. developed metal oxide type electroconductive pigment PASSTRAN (trade mark) Type-IV which is barium sulfate coated with SnOz(Sb) thin electroconductive layer. This paper shows about pigment characteristics and film condition of antistatic transparency paint which contained PASS TRAN.L.IntroductionRecently rapid development of electronics technology diffused electronic devices and products to Office, Factory, Laboratory and our life. But the other side, there are many problems for electronics parts which were caused electrostatic damage under static electricity. Demand of antistatic materials were become lager by this situation.There is close relationship between surface resistivity of material and static electricity. If the surface resistivity of object is enough low (under 109 Q /Sq), static electricity is dissipated quickly. So it is necessary for prevention of electrostatic charge to decrease surface resistivity of material using electroconductive coating.1) There are many type of electroconductive materials, for example, carbon black, metal powder, electroconductive polymer and so on. Especially, carbon black is used for general purpose by reason of its low cost, but it has big problem of black color. It can not get any color without black, and it caused contamination of carbon.In recent years, metal oxide electroconductive pigment (ECP) was developed and used for special purpose which demands transparent coating or easy dispersion to make ECP paint or endurance under hard environment and so on. Mitsui Mining & Smelting Co., Ltd. developed electroconductive pigment PASSTRAN Type-IV which is BaS04 coated with electro-conductive Tin oxide layer."

Jan 1, 1998

By Kazuyuki Kakegawa

"Sintered body of lead zirconate titanate (PZT) was prepared through the spark plasma sintering (SPS) technique. When the mixture of raw materials was calcined at 800°C and sintered at 900°C for 10 min. with SPS technique, the sintered body had almost theoretical density but was a mixture of lead titanate (PT) and PZT. When a calcining temperature of 1100°C was employed, sintered body had a single PZT phase but a lower density. High dielectric constant was obtained for a sample calcined at 800°C, sintered with SPS tecbriique and fired again in the air at 1100°C.IntroductionSpark plasma sintering (SPS) is a recently developed technique for sintering metals and ceramics1. The scheme of SPS is shown in Fig. 1. Sample is put in a graphite die in a vacuum chamber. It is pressed and pulse voltage is applied. The electric current heats the die. It is said that the pulse causes a spark-plasma between particles in the sample. Because of the spark- plasma, sample can be sintered at temperatures lower than that in the ordinary sintering by several hundred degrees of Celsius. The sintering period is also very short2Low sintering temperature and short sintering period in SPS technique cause low reaction rate. It is both disadvantage and advantage. In some cases, the reaction cannot be completed under the SPS conditions. If a mixture of several compositions having different properties can be sintered without a compositional change by the diffusion during the sintering, combination of properties, and therefore a design of property will be possible3. The low reaction rate of SPS may enable such combination."

Jan 1, 2000

By Ann M. Hagni

Reflected Light Microscopy (RLM) And Scanning Electron Microscopic-Energy Dispersive Spectroscopic Analysis (SEM-EDS) Study Of Electric Arc Furnace (EAF) Dusts Have Shown That Their Mineralogy Is Complex And Varied. The Particles Are Largely Spherical, And Can Be Seen In RLM Sections To Be Composed Of Franklinite, And Zincite, But They Show Significant Solid Solution With Each Other And May Contain Small Amounts Of Chromium. These Crystalline Phases Occur As Crystals And Skeletal Growths Within Ca-Fe-Si Glass. Because Chlorine Is A Deleterious Constituent In Recovered Zinc Products From EAF Dusts, Special Attention Has Been Given To Chlorine-Bearing Phases, And They Include Hydrophylite (Cacl2), Lime (Cao), And Organic Phases. Pyrohydrolysis-Treated EAF Dusts With Silica (Si02), Tungstite (W03), Alumina (A1203), And Bunsenite (Nio) Additives Contain Franklinite, Scheelite (Cawo4), Willemite (Zn2SiO4), And Hematite (Fe2O3)

Jan 1, 1992

By Hyun Kyu Shin, Byeong Deok Lee, Young Eun Lee

The reduction of Mn oxides at pre-smelting steps is an integral part of smelting processes for Mn alloys, and an understanding of its reaction mechanism is expected to contribute to the improvement of processing efficiency for Mn alloys smelting. The phase diagram shows that five Mn carbides are operative in the Mn-C system. Although they are expected to participate in the reduction of Mn oxides, no specific information is available yet to clarify their roles in presmelting carbothermic reaction of Mn oxides. Experiments with composite pellets prepared with Mn oxides and graphite powders show that Mn3O4 is reduced initially to MnO at about 1130oC and, subsequently, to Mn7C3 carbide as temperature increases further. At 1331oC, Mn7C3 carbide dissociates to Mn alloy and carbon. The degree of reducing reaction increases with increasing carbon balance in composite pellets and increasing temperatures.

Jan 1, 2014

By Takayoshi Fujii, Mitsumasa Hoshi, Chikashi Suenaga, Yoshiaki Suzuki

"In a bid to renovate its Saganoseki Smelter & Refinery and to establish a leading production unit in terms of global competitiveness, Nippon Mining & Metals undertook major - restructuring efforts since 1993.One of its themes was the shift from a two-flash furnaces operation to a single-flash furnace operation. The shift was successfully completed in 1996 while maintaining the production at the same level (330,000 metric tons per year of copper) by adopting such measures as improvements in pneumatic concentrate dryers, the concentrate feeding system, concentrate burners, the furnace cooling system, and a new cryogenic oxygen plant was constructed.With a view to realizing high matte grade operation (at 65%Cu) and increasing the concentrate feeding rate, further steps were taken the capacity of waste heat boiler was expanded and technical improvements were added, including optimization of the smelting reaction in the furnace shaft. As a result, the smelting capacity, as of the year 2000, has increased to 450,000 metric tons per year of copper.IntroductionThe feed rate to the flash furnace was doubled to 140 t/h from 70 t/h in 1996. Teething problems, as a result of the renovation, were almost solved by the end of 1996, and the operation of the single furnace operation has become stable.The main theme was the shift from a two-flash furnaces operation to a single-furnace operation to maintain the production capacity at the same level, namely 330,000 metric tons of copper per year. Then, in a bid to further renovate the Saganoseki Smelter & Refinery and to establish a leading production unit in terms of global competitiveness, further enhancement of the flash furnace's productivity was planned.The purpose of this plan was to raise the copper production capacity to 450,000 mtpy building on the potentialities of existing plants and without installing new equipment."

Jan 1, 2000

By S. J. Gerdemann

The U.S. Bureau of Mines is studying the kinetics of wet oxidation of sphalerite concen- trate (ZnS) as a possible process for a gravity-pressurized reactor (GPR). At tempera- tures in excess of 200' C, a sphalerite water slurry will react with 0, to form zinc sul- fate (ZnSO,). However, the pressure required to keep the water from boiling at these temperatures has kept this reaction from becoming a viable continuous process. The GPR can easily obtain the high pressures required for this reaction. The reaction rate is complicated by the solubility of 0, in water and the further oxidation of ZnSO, to insoluble zinc oxysulfate (Zn4(OH),S04.4H20). The effects of pressure, temperature, and particle size on the rate of reaction were investigated. Reaction rate was found to be limited by the amount of oxygen in solution. However, at 250" C and 1500 psia, over 90 pct of the zinc was solubilized in less than an hour. The conditions for maxi- mizing the Zn++ in solution, while minimizing oxysulfate formation, are discussed.

Jan 1, 1993

By C. Lupi

The electrorefining of primary copper is a well known technology: in this work copper scrap was directly processed in the same way. he copper and copper alloy scrap was previously pressed by means of a 20 tons apparatus in order to avoid pyrometallurgical operations. The samples obtained in this manner showed a good compactness so that they were used as anodes in the electrorefining tests. The tests were carried out on anodes made by copper scrap, copper alloy scrap and a mixture of the two. The electrorefining tests were performed at both 303 and 333 K, in a perspex cell having a volume of 500 ml using a current density of 250 A/m2. The cathode used was always a sheet of pure copper and the electrolyte composition was 40-50 g/l Cu as CuS04 and 150-200 g/l H2SO4. Current efficiency in the range of 92-97% and specific energy consumption ranging from 0.14- 0.20 kWg of copper were reached in all the tests. The refined copper deposits were analyzed by AAS to verify their purity and observed by SEM to highlight their morphology.

Jan 1, 1998

By Toshiaki Nakai, Kunihiko Takeda, Kimio Imaizumi, Hiroaki Shirasaka

"The new type of nano-porous silica particle was considered to be constructed by the spinodal decomposition-type process which was found to have narrower pores than those of conventional porous silica prepared from boron silicate or ""Shirasu"" balloon. Nano-porous silica particles were fabricated by the calcination of silica gel mixed with well-dispersed complex salts composed of phosphorous and molybdenum compounds. Both silica and inorganic salts were not perfectly dissolved in the suspension solution. After removing of the water, the silica-inorganic salts complex was volatized and successively calcinated at a temperature ranging from 650 °C to 800 °C. Then, the inorganic salts were removed by dissolving in hot water. Other inorganic salts such as potassium halides were also found to be effective as a pore-size controller.IntroductionControl of structure has an important role in the field of industry as well as in the separation and purification technology for metals and organic syntheses. Many studies on the control of material structures have been reported regarding porous materials with pores ranging from nanometer to micrometer scale. 1 ) One example is zeolite as a naturally yielded porous inorganic material. Various types of synthetic zeolites have been studied as ""molecular sieve"" materials with ordinary pore-size of less than one nanometer. In 1992, crystalline meso-porous material with a large surface area named MCM-41 was synthesized through the use of template synthesis. 2) In direct relation to our study, amorphous borate glass having 4 to 100 nm of fine pores known as Corning glass 3l or SiO2-Al2OrB2O 3-CaO porous glass having large pore dispersity ranging from 4 to 10,000 nm have been reported. 4 ) S) 6 ) Some examples of several reported studies are as follows: phase-separated porous glass consisting of B2OrAl2O3-ZrO2-RO-R2O complex oxide 7 ) glass with finer pore induced from hydrolysis of silane alkoxide, porous material attained by condensation polymerization through the use of sol-gel process 8), alumina meso-porous material 9 ) 10), silica-zirconia material 11), carbon porous material 12), etc.."

Jan 1, 2000

By E. A. Werner, W. Liebfahrt, J. Blaha

"The influence of the composition and the microstructure on the plane strain fracture toughness of five cold work tool steels all processed via the powder metallurgical route is investigated using 3-point bending specimens. The steels differ in composition and therefore possess different volume fractions of carbides. The amount, size and distribution of the carbides in the matrix are estimated by quantitative image analysis on a plane parallel to the fracture surface without discrimination of the carbide type, since the carbides are always much harder [1,2] than the matrix, irrespective of their composition. Due to the production of the steels via the powder metallurgical route almost all carbides are spherical in shape. The mechanical in-situ properties of the matrix are characterized by indentation tests performed with an ""UltraMicro"" -indenter in a scanning electron microscope.IntroductionCold work tool steels are used as tools in applications where excellent wear resistance and high hardness are required. Examples are cutting, woodworking, thread rolling, wire and deep drawing, cold extrusion and pressing of parts at process temperatures below 200°C. For such applications the steels must show an optimum combination of hardness, wear resistance and toughness while offering good machinability. Hardness and wear resistance are controlled by the amount of carbon and carbide forming elements such as molybdenum, tungsten, vanadium, chromium and niobium. These elements are present in the MC-, M6C and M7C3-carbides and are also responsible for the precepitation of secondary carbides during tempering. In this report attention is paid to the influence of the primary carbides only, while the very small ~~nm) secondary carbides will be treated as constituent of the homogeneous matrix. Increasing the amount of carbides (alloying elements) usually results in a decrease of the material's toughness which is caused by the presence of clusters and/or bands of carbides. To achieve an optimum combination of hardness, wear resistance and toughness many of the today's cold work tool steels are processed via the powder metallurgical (PM) route, which helps to prevent non-uniform element/carbide distribution because of the rapid solidification of the powders used. The resulting microstructure of the tool steel then consists of a tough matrix with uniformly distributed hard carbides· of globular shape. This shape of the carbides is also desirable instead of blocky carbides present in non-PM tool steels, since they improve the machinability of the steel. An additional advantage of PM-steels lies in the possibility to produce near net shaped tools thus lowering the costs of machining."

Jan 1, 2000

By Ashish D. Patel, Ramesh S. Minisandram

"Vacuum Arc Remelting (VAR) is the final and, hence, critical melting step for the production of a sound, segregation-free ingot for the manufacture of alloys used in rotating components in aircraft engines. A mathematical model for this process has been developed by the Specialty Metal Processing Consortium (SMPC). The model predicts temperature distribution in the solidifying ingot, flow in the molten metal pool, and the electromagnetic field in the ingot. These predictions may be used to estimate the effect of melting parameters on the pool profile in the ingot. In this paper, typical pool shapes and flow fields during VAR of Alloy 718 and Ti-6Al-4V are presented. The differences in the pool profile are primarily due to vastly different melting conditions. The model predictions are compared to the observed pool shapes from industrial-size VAR ingots.1. IntroductionVacuum Arc Remelting (VAR) is a process in which an electrode is melted in vacuum by the heat from a DC electric arc. Metal droplets from the electrode fall into the molten metal pool, which solidifies in a water-cooled copper crucible to form the ingot, as shown in Figure I. The ingot obtained from VAR is sound, and has superior cleanliness and chemical homogeneity. Hence, the process is the final melting process for most nickel-base superalloys and titanium alloys used in the manufacture of critical rotating components (discs & blades) of aircraft engines. Modeling of this process provides an insight into the effect of melting parameters on the molten metal pool in the solidifying ingot, which is a key first step in process optimization and defect prevention. In this paper, typical pool shapes, both measured and predicted, for VAR of Alloy 718 and Ti-6Al-4Vare presented. Alloy 718 is the most common VAR-processed nickel-base superalloy; whereas Ti-6Al-4V is the ''workhorse"" alloy for titanium-based alloys."

Jan 1, 2004

By Guangchun Yao, Chuan Li, Hongjie Luo, Zhuokun Cao

"The expansion rate and collapse time of liquid aluminum foams are essential for the determination of operating time and quality of the resulting foam. In the present paper, liquid aluminum foams was fabricated by adding in TiH2 as blowing agent, and the variation of expansion rate with foaming time was non-contact detected by a laser distance measurer. The influence of different stabilizing agent and alloying elements was studied. The results show the fact that the fraction of stabilizing agent only perform little effects on the maximum expansion rate of liquid aluminum foams, while the influence of alloy elements are remarkable. The maximum expansion rate would increase much when Mg is added, and the liquid foam also collapse at a shorter time. Comparison was made between experimental results and mathematic calculations, which reveal the fact that it is the change of TiH2 decomposition responsible for the change.IntroductionMetal foams, combining light weight with other unique mechanical and physical properties, have gained wide interest and been developing fast during past few decades. However, manufacture of this new material is quite challenging since it involves simultaneous occurrence of gas, liquid and solid phase at high temperature [1-2].Quite some manufacture routes have been developed for manufacturing metal foams, and the structure and quality of resulting foam are remarkably improved during the last decades. However, most of the past works seems to be experiential, and because the lack of basic knowledge of foaming process, the start material is limited and the production technologies are far from reliable and reproducible.[3-4]In direct foaming process, decomposition of blowing agents, TiH2 for example, is the main force for foam expansion. The density and foam structure changes with time during the foaming process, so it is expected that foams of certain structure can be obtained by solidification of the liquid foam at a certain time [5-6]. However, the foaming process is weak in reproducibility and the influence of stabilization additives and alloying elements is unclear."

Jan 1, 2011

By C. B. Catanach

The development and in place leaching of a chalcocite ore body at Mountain City, Nevada is described. Block caving was used to induce permeability while ore removed during development was leached in heaps on the surface. Copper was recovered by precipitation on iron. Excess ground water which seeped into the mine was pumped into a deep disposal well. A parallel system was used to purify water by lime neutralization. Copper extraction was at an annualized rate of 11% during the first six full months of underground leaching and totalled approximately 30% during six months of heap leaching. Leach solution flow and distribution had a major effect on extraction rate. Enrichment of leach solutions with ferric sulfate did not produce conclusive results until analyzed with the aid of a leaching model.

Jan 1, 1976

By Fumiatsu Sato

In recent years, an increasing number of urban soil contamination cases have been found during redevelopment of former factory sites. Hydroclassification technique, separating heavily contaminated fine soil particles from contaminated sites, is one of the economical remediation techniques for contaminated soil by heavy metals, but the separated fine soil particles are generally landfilled because of the difficulty in removing strongly adsorbed heavy metals on them. In the previous study, the authors have investigated the mechanism and the optimum condition of chlorination-volatilization technique to eliminate heavy metals from inorganic waste and found it was needed to heat up around 1273K. In this paper, a new remediation technique for lead contaminated fine soil particles is proposed. This technique is composed of chlorination and subsequent warm water extraction. In the chlorination step, water-insoluble lead complex is chlorinated to be water-soluble lead chloride without volatilization, by heating the soils with MgCl2-CaCl2-KCl salt mixture at relatively low temperature. By subsequent warm water extraction, lead chloride is leached out. Effects of chlorination conditions, such as time, temperature, composition of the salt and added salt ratio, on lead behavior were investigated. It was proved that lead concentration could be reduced below Japanese environmental standard.

Jan 1, 2006

By R. Upadhyaya

Aluminium alloy matrix cast composites have been synthesised by incorporating fine graphite powders (0.5 - 20 µm size) and chopped carbon fibres (6.5 pm P). 3-6 mm length) by liquid metallurgy technique. Incorporation of these second phase materials exceeding 6-8 wt% invariably resulted in agglomeration of the dispersoids and sometimes leading to even total rejection. It was found that small additions of mischmetal (1-3 wt%) during dispersion resulted in better incorporation without much agglomeration of the dispersoid as evident from the macro and micro structures of the composites. Further, the additions of mischmetal increased the volume of the effective incorporation of the dispersoid even to the extent 50- 60%. The mischmetal addition results in a significant increase in the power factor of the stirrer motor indicating an apparent increase in the viscosity of the system. The higher viscosity of the melt increase the shear transmission conditions within the melt during stirring thereby breaking the agglomerates of the dispersoids. The increased viscosity of the melt seems to be due to the formation rare earth - aluminium inter metallics precipitation, as observed in the metallographic studies, thereby making the process a "pseudorheocasting? technique. A provisional patent has been filed based on this work.

Jan 1, 1989

By Sungdon Kim, Chuljoo Kim, Joonsoo Kim, Hosung Yoon

"This study was performed to establish the optimum leaching condition through the experiments for the oxidized roasting followed by leaching of fluorocarbonate rare earth mineral (bastnasite) using sulfuric acid, and to establish the optimum condition for the recovery of cerium by ion- sieve method from the leached solution of bastnasite. The optimum conditions for the sulfuric acid leaching by the oxidizing roasting of bastnasite concentrates are that the roasting temperature is 550 -600 °C, the roasting time is 2 hrs, the concentration of sulfuric acid is 6N, the leaching temperature is S0°C and the leaching time is 3 hrs. At this time, the leaching yield of total rare earth oxides in the leaching of bastnasite concentrates is about 91%. When cerium is recovered by ion-sieve method from the solution obtained by the sulfuric acid leaching of the roasted bastnasite, the optimum conditions are that the TREO(total rare earth oxide) of leached solution is below 70 g/l, the flow rate of leached solution is 9.6 ml/min and the ratio of height to diameter of resin packed in column is above 9. In these conditions, the recovery of cerium of yield 85% and purity 96% is possible.IntroductionThe rare earths are generally called to Lanthanides, which are totally 17 elements including Scandium of atomic number 21 and Yttrium of atomic number 39 in addition to 1 S elements from Lanthanum of atomic number 57 to Lutetium of atomic number 71. Since the separation to each element is very difficult because of their similar chemical properties, the rare earths were used as the mixed rare earths and the mischmetal without separating to each element. However, the high purity rare earths are recently produced commercially to each element so that they are used as the materials for high tech. industry such as electric and electronic materials, catalysts, optical materials, special alloy and 8Uperconductive materials, and their consumption is rapidly increasing. Therefore, the purpose of this study is firstly to prepare leached solution by using the series of process of the oxidation-roasting and leaching by sulfuric acid. Next, second purpose is the separation and recovery of cerium by ion-sieve method."

Jan 1, 1998

By Yuanbo Zhang, Ruijun Wang, Qian Li, Zhao Jing, Guanghui Li, Zhengwei Yu, Chen Liu

The high content of sodium and potassium in sinter is harmful for blast furnace ironmaking. Reductive sintering technology can remove more alkali metals than conventional sintering process. In order to improve the removal ratios of Na and K, reductive sintering with both CO-containing flue gas circulation and carbon-bearing pellet was conducted in this study. Experimental results show that all indexes except the VSV and P were improved in reductive sintering with CO circulation. Flue gas circulation technique combined with carbon-bearing pellets were beneficial to reductive sintering, because it could maintain good sintering indexes and enhance the removal of Na, K. The best removal ratios of Na, K and reduction degree of iron oxides were 20.37%, 63.73% and 23.76%. In reductive finished sinter, silicate mineral becomes the important binder phase, and main iron mineral phases are wustite (FexO) and magnetite (Fe3O4).

Jan 1, 2016

By Raymond M. Coveney

Bedded sulfide ores in Cambrian Chinese black shales typically contains at least 2% Ni, 4.5% Mo, 1% As and 0.2% Se. Thin laminae and replaced on colites from the ore contain intimate mixtures of fine-grained Ni-rich sulfides and jordisite complicating ore treatment. The ores contain abundant jordisite, vaesite, nickelian pyrite, and barite and lesser amounts of sphalerite, gersdorffite, millerite, tennantite, fluorite, chalcopyrite, and HgSe (probably tiemannite). At present only ores that are sufficiently rich (>4.5% Mo) for direct roasting are mined and treated to produce, ammonium molybdate. The ores contain Pt, Pd, and Au in amounts totaling up to -2.5 ppm, but these are not recovered.

Jan 1, 1993

By Xiaodi Huang, Matthew Andriese, Zheng Zhang, Jiann-Yang Hwang, Zhiwei Peng

"The thermal decomposition and regeneration behaviors of wüstite were investigated by in situ high temperature X-ray diffraction (HT-XRD) under non-isothermal condition at heating rate of 4 K min-1 in vacuum ranging from 294 K to 973 K. Wüstite on heating decomposes to magnetite and iron up to 823 K, above which it exhibits marked tendency to regenerate. Investigation of thermal stability of the reaction system shows that the decomposition proceeds under kinetic reaction control while the regeneration is under thermodynamic control. Kinetics study based on the Coats-Redfern integral approximation method indicates that the decomposition reaction follows a Komatsu-Uemura model-based diffusion-controlled kinetics with activation energy of 32.860 kJ mol-1. The thermodynamics analysis of regeneration reaction demonstrates that wüstite regenerates at lower temperature than stoichiometric ferrous oxide.IntroductionOwing to its importance in preparing various magnetic ceramic/metal nanocompostites or nanocrystals with high values of coercivity for the application as recording media, wüstite (non-stoichiometric ferrous oxide) has been attracting the attention of scientists over a long period [1-6]. The thermal behavior of wüstite was investigated by several researchers and phase transformations due to thermal decomposition and regeneration of wüstite during the heating in a specific temperature range was observed [7-9]. In spite of wüstite being found to dissociate to magnetite and iron at temperatures lower than 848 K and then regenerates at higher temperature, a clear understanding of the reaction mechanisms is clearly lacking [9]."

Jan 1, 2012

By Cameron Harris

With the consolidation of the copper industry in the second half of the 20th century resulting in fewer plants treating ever increasing quantities and qualities of feed, the enormous flexibility of the Noranda Process gives it significant advantages over many competing technologies for the production of matte. Toll smelting, recycling, and secondaries treatment will become the cornerstone of profitable operations for all but the lucky few who have large captive mines associated with the smelter. Consequently, the ability to respond to changing market conditions without significant metallurgical or operational upsets will be of considerable commercial advantage. The inherent stability of this bath-smelting process leads to tight matte grade control, while the bath turbulence leads to rapid consumption of feeds with widely varying physical characteristics. Low capital and operating costs combined with a layout suitable for retrofit into existing converter aisles makes it a sensible choice for parts of the world still experiencing the aforementioned consolidation, which is essentially complete in fully developed economies such as the United States of America and the European Union. This paper will discuss features of the Noranda process compared with other technologies and its place in the future global copper production industry, which is set to become increasingly competitive and aggressive.

Jan 1, 2002

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