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By Tomoji Kawai

"The Pulsed Laser Deposition method using multi-targets is extremely useful for the creation of functional multi-layers and variety of artificial lattices. The topic of the present talk is on the creation of ''Function hannonized artificial lattices by laser ablation"" made of the combined magnetic, ferroelectiric and superconducting layers. The outline of talk is,1. Features of Pulsed Laser Deposition method (Laser Molecular RHEED and S1M/AFM.2. Creation of magnetic, dielectric and superconducting artificial lattices by Pulsed Laser Deposition.3. Novel properties of function harmonized artificial lattices: especially on the magnetic and magnetoresistive artificial The outline of talk is, lattices made of3d transition metal oxides."

Jan 1, 2000

By Hong N. Vu, Jitka Jandova

"Gypsum and limestone methods were examined in this study to process zinnwaldite wastes originating from dressing Sn-W ores mined in the Czech Republic. These wastes containing 0.20-0.30% Li and 0.10-0.20% Rb were subjected to magnetic separation to obtain a zinnwaldite concentrate with 1.36% Li and 0.94% Rb. It was observed that processing of the zinnwaldite concentrate with gypsum resulted in almost 96% recovery of Li into aqueous liquors, whilst rubidium extraction was only 25%. At the same time, it is possible to extract almost 92% Li and Rb from the identical zinnwaldite concentrate if the concentrate is processed by limestone method. Lithium carbonate, a final product of both methods was recovered from the refined sulphate solution using K2CO3 as a precipitation agent and/or from unrefined hydroxide solution using gaseous CO2. In the continuation of this study, rubidium will be separated from carbonate solutions after Li2CO3 precipitation as RbAl(SO4)2, an intermediate for Rb2CO3 production. IntroductionLithium is used as an alloying constituent in lightweight alloys, as a heat transfer medium in nuclear reactors and as a component in primary and secondary batteries. With the development of a new generation of electric vehicles, the lithium demand will dramatically grow. Lithium chemicals find extensive application in many industrial branches such as metallurgical, glass, ceramic and pharmaceutical industries. Rubidium compounds are predominantly used in psychiatry and medicine, in magneto-optic modulators, solid-state lasers, phosphors and components of electrolytes for fuel cells. The four most important lithium minerals are amblygonite, spodumene, petalite, and lepidolite. Spodumene LiAlSi2O6 (6.0-7.5% Li2O) and petalite LiAlSi4O10 (3.5-4.5% Li2O) belong to aluminosilcate minerals. Lepidolite (Li.Al)3(Al.Si)4O10(F.OH)2 (3.30-7.74% Li2O), lithium mica, is the most important representative of the mica minerals, a subgroup of the aluminosilicates. It frequently contains 3–5% Rb2O and eventually caesium. Zinnwaldite, which has the general formula K(Li.Al.Fe)3(Al.Si)4O10(F.OH)2 (2-5% Li2O), is regarded as a variety of lepidolite with a high iron content. Commercial amblygonite is a complex phosphate (Li.Na)Al(F.OH)PO4 (up to 9.88% Li2O), however, its deposits have not been commercially exploited because of their small size. Natural brines with a high lithium chloride content are important in the industrial production of lithium [l]"

Jan 1, 2008

By Min Chen, Zhen Tian, Hongxu Cui

"The effects of adjusting technology on the phosphorous enrichment in converter slag were investigated. The results showed that the grain size of 2CaO·SiO2 with high phosphorus containing content increased slightly with the decreasing of cooling rate, and the proper cooling rate was confirmed to be about l.0°C.min-1. Moreover, the morphology of the phosphorus-rich phase of 2CaO·SiO2-3CaO·P2O 5 was changed from granular for the higher basicity of converter slag to the coexistence of granular shape and rod-like for the lower basicity of adjusted slag. With the addition of adjusting agent such as SiO2 to lower the basicity of converter slag, the phosphorus in converter slag could be transferred into 2CaO·Si02 phase effectively, and P2O 5 content in high phosphorus containing phase reached to above 30%.IntroductionThe yield of converter slag is very large in China, but most of the slag is stacked usually after the separation of iron, which not only takes up a lot of land, but also affects the ecological environment seriously. Therefore, improving the comprehensive utilization and value-added products of converter slag is of great significance to recycle the steelmaking slag[l-3]. On the other hand, the refining of hot metal with high phosphorous content is an unavoidable problem with the decreasing of high grade iron ore, and as a result, more amounts of high phosphorus containing steelmaking slag are produced. However, the current recycle of converter slag is more focused on the emission reduction and reuse of steelmaking slag inside the iron and steelmaking process without considering the recycle of phosphorous resources[4-6]. At the same time, the development and utilization of phosphate ore as a strategic resource is drawing more and more attention, but the phosphate ore in China is mostly low grade and significant amounts of tailings are produced which is harmful to the environment. Therefore, it is important to separate phosphorous resources in steelmaking slag which can be used as phosphate ore for fertilizer material[7-9].Literature studies showed that most of the phosphorus in steelmaking slag existing as 2CaO·SiO2-3CaO·P2O 5 solid solution phase in 2CaO·SiO2 particle. The P2O 5 content in the phosphorus containing phase is very low due to the fact that the basicity of converter slag is usually high and the precipitated amounts of 2CaO·SiO2 particles during cooling are very large, resulting in the fact that the P2O 5 contents in 2CaO·SiO2-3CaO·P2O 5 solid solution phase are much lower which is impossible to be used as phosphorous resources instead of phosphate ore. Thus, the enrichment of phosphorus in steelmaking slag is need[ 10-14]."

Jan 1, 2011

By Shadia J. Ikhmayies

"Cadmium sulfide (CdS) in the form of thin films is an interesting material because it has a large variety of applications ranging from photovoltaic to luminescent devices. N-type CdS is usually used as a window layer in the heterojunction CdS/CdTe thin film solar cells. A review of the photoluminescence (PL) spectra ofn-type CdS thin films prepared by different techniques was performed. The effects of different dopants and impurities and the effects of temperature and deposition parameters on the PL spectra were discussed. Annealing in different atmospheres causes the changes in material structure and phase change from cubic to hexagonal phase which can be detected through the variations in the PL spectra. CdCh heat treatment improves the cystallinity of the films and enhances the exciton peaks and the green band in the PL spectra.IntroductionThin CdS films deserve attention because their expected gap emission lies very close to the highest sensitivity of the human eye. Thus, one might assume that thin CdS films are an appealing host for photonic devices [ l]. They have been used in a lot of applications including electronic and optoelectronic devices [2]. Thin films ofn-type CdS are widely used as a window layer in heterojunction solar cells such as CdS/CdTe solar cells. Doped and undoped CdS thin films can be obtained by different techniques such as; spray pyrolysis (SP) [3], chemical bath deposition (CBD) [2, 4], pulsed laser deposition [5, 6, 7], laser ablation [l], thermal evaporation [8].Several experimental techniques have been used in order to study semiconductor defects. In particular, photoluminescence (PL) has been shown as a powerful and sensitive tool in examining the crystal quality of polycrystalline thin films. PL can be used in the detection of defects which are radiative active. These defects can also act as traps in the transport of carriers [9]. The photoluminescence (PL) of thin film CdS is strongly influenced by the unbalanced stoichiometry, which is typical for CdS and is in general evoked by a Cd surplus. With increasing Cd content, the emission spectra move far below the gap to the red spectral range. Besides stoichiometry problems, independent of the material deposited, the PL properties of thin films depend on surface features and the influence of the interface between the film material and the substrate [10]."

Jan 1, 2013

By Hanlu Xie, Liang Yu, Ping Wang, Yuanchi Dong

"The leaching process is the first step when recycling BF slag as raw material for some other products. While studying the kinetics of the BF slag leaching process, a fractal phenomenon was found, which indicated some interesting mechanism in the process. The result suggested a new understanding of the leaching process in detail which useful for the industrial applicationIntroductionTypical composition (wt. %) of blast furnace slag varied in a pretty wide range: SiO2 30–40, Al2O3 10–20, CaO 30–40, MgO 5–10.The ground granulated slag is commonly used as base of roadway (mixed with natural inert for paving, soil stabilization, etc.) or one of the resources of Portland cements because of its good hydraulic activity [1]. To recycle the slag economically, the selective recovery of some components of the slag may be considered. As main components exist in the slag, silica [2, 3 and 4] and alumina [4] recovery was first considered.While recovering of silica from the slag, silica gels are recovered selectively from the leaching solution deriving from the treatment of the slag with waste sulfuric acid. After separation of the exhausted solid of leaching, the silica gel is precipitated from the solution at pH 3.2. Although the silica gels obtained by this procedure contain many impurities and need some more work afterward, it is the first and important step for the process.In the prior work [5], silica extraction using blast furnace slag had been investigated, focused on the pH value of selectively silica extraction. In the present work, kinetics of the leaching process was focused. It is important to design an economical process.ExperimentalThe composition of the slag and the calcined gels has been determined by a LINK860 (Oxford Instruments, Oak Ridge, TN) energy dispersive spectrometer (EDS) in conjunction with a CAMBRIDGE S250-M2 (Cambridge Instrument Ltd., Cambridge, U.K.) scanning electron microscope(SEM). The leaching of slag and the precipitation of silica gels have been conducted at atmospheric pressure in a stirred reactor placed at temperature controlled by a heated water bath."

Jan 1, 2008

By Petr Sulovsky, Jaroslava Ledererova, Miroslav Svoboda, Michaela Suchardova

"The thinning resources of natural raw materials necessitate an increased degree of waste material recycling. The building industry offers a range of technologies enabling incorporation of industrial wastes into building materials for construction purposes in an economically acceptable way. Our research is focused on finding the appropriate technologies for specific groups of industrial waste materials (IWM). The studied IWM involve coal combustion residues (CCR), desulphurization products, sludges, metallurgical slags, and various other wastes. Many of them contain increased amounts of toxic elements that can under certain conditions get released. In order to prevent this, each specific IWM requires finding the technology that best ensures the binding of toxic elements in the building matter are fixed for the long term.Introduction The sustainable development of mankind is more than ever viewed as a matter of resources. Many aspects of the switch from a throw-away to a recycling society concern one of the largest consumers of natural resources and producer of greenhouse gases, the building industry. One of the biggest tasks lying before the researchers in the field of building materials is to find substitute or alternative raw materials that would save the thinning reserves of natural resources. The most promising and natural way is to replace the traditional raw materials with rejected and unwanted products of industrial processes, classified as wastes. These of course are not produced with the primary intention of achieving some desired properties. The usage of industrial wastes therefore involves finding the optimal way of usage their existing positive (from the point of view of utilizations) properties and minimizing the impact of their undesired properties, i.e. from the perspective of the considered application."

Jan 1, 2008

By D. D. L. Chung

"In-situ network composites are composites in which the filler network is formed during composite fabrication, in contrast to ex-situ networks which are formed prior to composite fabrication. A homogeneous in-situ network composite has the entire network at the same composition; a heterogeneous in-situ network composite has different parts of the network at different compositions. The homogeneous network composite is made either by the Method of Molten Filler Flow or the Method of Dissolution and Deposition; a heterogeneous network composite is made by the Method of Liquid-Phase Networking. Examples include polymermatrix and metal-matrix composites.IntroductionNetwork composites refer to composites containing a continuous three-dimensional network as the filler. These composites are attractive in their lack of delamination failure, which is usually characterised by two-dimensional composites. The filler and matrix in a network composite can be considered two interpenetrating networks. The mechanical interlocking of the networks adds to the cohesion of the composite. In cases where the filer is much better than the matrix in a certain property, the network nature of the filler makes the filler highly effective in improving that property in the composite in all directions. The property desired in the composite may be high strength, high modulus, low coefficient of thermal expansion, high thermal conductivity, or low electrical resistivity."

Jan 1, 1994

By Michael A. Markowitz, Alok Singh

"Molecular self-assembly of phospholipids and other amphipathic molecules offers a versatile approach to form self-organized microstructures in various morphologies. Stabilization of microstructures in specific morphologies by polymerization renders them useful for practical applications in areas ranging from controlled release technology to template mediated synthesis of metals. Our efforts are focussed on the development of polymerizable biomembranes derived from phospholipids, their properties and utility e.g., as stable templates for studying chemistry at the lipid interface. Polymerized vesicles formed from mixtures of 1,2-bis(tricosa-1 O,12-diynoyl)-sn-glycero-3-phosphocholine, 1, with corresponding lipids having phosphohydroxyethanol,2, or -hydroxypropanol,3, headgroups have been used in electroless metal plating of vesicle surface with gold utilizing selective binding of Pd(NH3)4 2 + to 2 or 3. The surface bound palladium ion served as catalyst for metalization. Metalization of polymerized vesicles constructed from charge neutral diacetylenic phosphocholine,1, did not occur using this process. The headgroup structure of the negatively charged phospholipids and the degree of vesicle polymerization had an effect on the stability of the vesicles after metalization. Vesicles formed from a mixture of 1 with polymerizable diacetylenic phosphatidic acid, nonpolymerizable 1,2- dipalmitoyl phosphohydroxyethanol or 1,2-diacyl phosphohydroxyethanol (from soy lecithin) were not stable to metalization process. The metal coating of the vesicles was examined by electron diffraction and revealed that the gold metal on vesicles was polycrystalline and face centered cubic. The results demonstrate the utility of polymerized synthetic membranes as template for easy and efficient synthesis of nanoparticles. IntroductionPhospholipids, synthetic or natural, provide a simple and straight forward route to construct membranes in a variety of morphologies due to their inherent property of selforganization in the presence of water[1]. Vesicles are closed spherical structures comprised of concentric walls made from lipid bilayers. Vesicles are morphologically simple structures with enormous technological potential. Polymerizable phospholipids prepared by incorporating a polymerizable group in the molecules demonstrate physical properties comparable to their non-polymerizable counterparts and have the added virtue of providing enhanced physical and chemical stability to the membranes[2,3]. The size, shape and properties of the organized assemblies are dependent on the lipid structure and the nature of the aqueous environment[4,5]. The headgroup geometry, surface charge density, and spatial arrangement of the phospholipids are known to affect the surface behavior of the lipid membranes, which is evident through their interaction with other molecular (hormones, antigens, antibodies etc) or lomc species. Since phospholipid headgroup structure and charge can be modified either synthetically or by chemical perturbation of the aqueous medium (e.g., pH or ionic strength), phospholipid membrane surfaces offer a potential for developing novel strategies in those areas which involve the use of molecular reactive sites. One such strategy which could be envisioned explores the use of molecularly engineered phospholipid assemblies to design and prepare template structures to regulate formation of ordered materials [6]."

Jan 1, 1994

By Toshiki Kabutomori

In fuel cell powered automobiles, hydrogen is required to be stored in materials that have a hydrogen storage density of over 4 mass%; further, these materials should be capable of supplying hydrogen by using the waste heat from a fuel cell, which is at a temperature of 373 K, in order to match the mileage of gasoline-powered vehicles. A Ti-Cr-V alloy, which exhibits a BCC structure and forms a solid solution, is a promising candidate for onboard hydrogen storage materials. Although it has a large hydrogen storage capacity of over 3.9 mass%, the rechargeable hydrogen capacity is limited to approximately 2.6 mass%. In this study, the effects of fine pulverization of the alloy on PCT (hydrogen pressure-composition-isotherm) characteristics were investigated in order to improve the rechargeable hydrogen storage capacity of the alloy. From the PCT measurements of the finely pulverized samples of the alloy, a plateau in the absorption curve was observed to begin at a hydrogen concentration of 0.5 mass%; further, a rechargeable hydrogen storage capacity of 3.3 mass% was obtained. This was greater than that obtained from the sample that was not finely pulverized, i.e., 2.5 mass%. However, the plateau width in the desorption curve was 2.5 mass%, which was the same as that observed for the sample that was not finely pulverized. The increase in the rechargeable hydrogen capacity during absorption is attributed to the precipitation of the -hydride phase (MH~2) directly from the metal phase (phase). The precipitation of the phase (MH~0.5), which should be formed in low hydrogen concentrations, is suppressed as a result of a possible reduction in the internal defects such as dislocations, vacancies, and grain boundaries by fine pulverization and annealing of the alloy.

Jan 1, 2006

By G. L. Watt

Fine sized titanium diboride (TiB2) powders have been synthesized in a thermal plasma reactor. Precursor for the synthesis were rutile, boron oxide, and methane. The effect of plasma gas type, precursor ratio, and input power on the synthesis was studied. The produced powders were characterized by X-ray diffraction and chemical analysis. The purified powders were CIP'd, HIP'd, sintered and characterized for porosity, hardness, and microstructure and the results compared with a commercially available TiB2 powder sample.

Jan 1, 1995

By Robert T. Oxnard

"EXECUTIVE SUMMARYThe history of Refractory Recycling indicates there was little recycling until the 1950s. Energy incentives were the primary reason for the beginnings of a recycling effort by the refractory brick manufacturers. Quality benefits quickly became evident and fewer rejects were the result. Today, economic factors including higher valued raw materials and increased competition are the driving forces of refractory recycling.There are some success stories in refractory recycling but we have a long way to go. Few incentives, quality concerns, relatively cheap energy, comparatively lax government regulations, inexpensive landfills and inexpensive substitutes make recycling a difficult choice for many companies. Marketing advantages such as ISO 14000, eliminating multiple audits and reduced liability exposure can tip the scales toward recycling viability. Increasingly, the ideological philosophy of a company, a desire to minimize environmental impact and develop favorable public and other interested party perceptions can drive recycling and waste minimization efforts.Recycled materials can be more trouble ""up front"" and harder to ""manage"" due to their suspect quality. However, due to their nearly inexhaustible supply and the fact that once developed, they constantly contribute to the bottom line, they are certain to be the materials of the future. Waste refractory materials will likely see the same bright future as the steel scrap yards and slag piles of yesterday. In hindsight, we will realize that now was the perfect time to prepare and plan for the bright future of refractory recycling."

Jan 1, 2000

By Norbert L. Piret

During smelting of copper, arsenic in the feed reports to a large extent to the gas phase and some enters the anode copper. From the gas phase it is transferred during wet gas cleaning directly, or indirectly after dust processing, to aqueous solution. During the electrorefining and anode slimes processing, the anode arsenic content is also transferred to aqueous solution. Technology for the efficient removal of arsenic from process streams and cleaning of aqueous effluents is well established. However, the arsenic-bearing products, which thereby are generated, can vary widely in consistency, quality and quantity, from large amounts of gypsum contaminated with water-soluble arsenic compounds to residues with high arsenic content ' or arsenic products. Arsenic management in a copper smelter not only is involved with the duty of compliance to the gaseous and aqueous emissions standards but also should have as objective the minimization of the generation of arsenic-bearing and, in general, heavy metal-bearing solid waste. The present paper outlines options and the associated economic aspects for minimization of arsenic-bearing solid waste generation, for improvement of the environmental compatibility of the residues to be deposited and for the .production of commerciable arsenic compounds under appropriate market conditions.

Jan 1, 1999

By E. Kozeschnik

A new model is presented for the simulation of the evolution of precipitates in a multi-component multi-particle multi-phase environment The mathematical formulation as well as the physical background of the model are briefly introduced and its capabilities are discussed on the example of a precipitation sequence in a complex steel. Keywords: Modeling, precipitation kinetics, nucleation, growth, coarsening

Jan 1, 2003

By Martin Brueggemann

The Tyrone copper solution extraction and electrowinning plant was the first such facility built by Phelps Dodge Mining Company in 1984. Over the next 20 years, the aqueous flow rate capacity of the plant has been expanded from the original design of 12,000 gallons per minute (gpm) to 34,000 gpm to meet production goals in the face of declining copper grades in the leach solutions. The ability to process higher aqueous flow rates through existing equipment comes at the expense of increased organic loss through entrainment to raffinate. These losses of organic (diluent and extraction reagents) can account for up to 10 percent of the plant?s total operating costs. With the recent dramatic price increase of petroleum-based products, these operating costs due to losses are sure to increase. This paper will discuss recent improvements at the Tyrone SXEW plant that have resulted in a 40 percent reduction of organic losses. These improvements include picket fence modifications, new fence materials, organic recovery systems, and operational practices within the solution extraction process.

Jan 1, 2006

By Alana Pereira Ramos, Walman Benicio de Castro

Amorphization and martensitic transformation (Ms) characteristics of Ti–Ni-Cu alloy ribbons prepared by melt spinning were investigated by means of differential scanning calorimetry and X-ray diffraction. In these experiments particular attention has been paid to change the wheel linear velocity from 21 to 63 m/s. Then the cooling rates of ribbons were controlled. The effect of this cooling rate and alloy composition on martensitic transformation behavior is discussed.

Jan 1, 2015

By A. Cullaj

During a period of 15 years the metallurgical and chemical complex of Elbasan containing more than 15 principal plants, producing cast-iron, steel, coke, nickel carbonate, nickel, cobalt, chromium and other products, discharged into air, river water and soil an extensive amount of hazardous wastes containing high toxic substances. A monitoring study for the levels of heavy metals in soils nearby the former plant is carried out for the first time. Very high levels (total and extractable) of contaminants such as nickel, cobalt and chromium are found in samples taken from a relatively vast territory including the city of Elbasan, situated 8 kilometres far from the plant. The most polluted samples present a total content of 1211.8 ? 2949.6 mg/kg Ni, 97.0 ? 181.2 mg/kg Co and 1358.7 ? 4130 mg/kg Cr. These levels exceed several times the phytotoxic thresholds and present a potential hazard for the inhabitants. This study, as part of a bigger multinational project on solid decontamination, will also serve to the possible application of the new phytoremediation and phytoextraction technologies, being developed in parallel in this project.

Jan 1, 2006

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

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

Jan 1, 1999

By Mim Li, Huimin Lu, Lisha Yang

"CuInS2 thin films solar cells have drawn much attention for their low-cost, stability and high conversion efficiency. The electrodeposition of Cu-In precursor films, as the first step in making CuinS2 solar cells electrochemically in the air-and water-stable ionic liquid based on choline chloride/urea eutectic mixture has been investigated at constant potential. Compared with aqueous electrolytes, the large electrochemical window as well as the high thermal stability of this ionic liquid allow the direct electrodeposition of Cu-In precursor films. Then the precursor films were sulfuretted in a tube furnace at different sulfurization temperatures to optimize the films properties. The films obtained were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), energy dispersive spectroscopy (EDS).IntroductionCuInS2 is one of the most prospective absorber materials for low cost thin film solar cells, with a high conversion efficiency that exceeds 32% in terms of theory and nearly 13% in laboratory level [1-2]. In addition to its long-term stability, CuinS2 has a band gap energy Eg ranging from 1.3 to 1.55 eV and an optimal optical absorption coefficient reaching 105cm-1 [3-4]. CuinS2 thin films have been prepared by several methods such as spray pyrolysis [5-6], r.f.sputtering [7], vacuum evaporation [8-9] and electrodeposition. Comparing with vacuum methods, electrodeposition has lots of advantages such as less energy consumption, preparation big area thin film, stable system and enabling cheaper films.The electrodeposition of most technologically important metals has been shown to be possible from a wide range of ionic liquids. These ionic liquids are currently applied in a wide variety area. It is reported that the cell efficiency of chalcopyrite absorber layer (CIS, CISeS, and CIGS) via an electrodeposition route in laboratory condition has reached 11.3% [10]. Copper and indium alloy film is regarded as important precursor for the production of compound semiconductors with sulfur. The electrodeposition of the alloy film from room temperature ionic liquid (RTIL) has not been widely investigated. Only few alloy films, such as ZnTe, CdTe, GaAs and AlSb have been electrodeposited."

Jan 1, 2011

By JiaPeng Xu, Brian Lo, Uday B. Pal, Yihong Jiang, Soumendra N. Basu

"The Solid-Oxide Oxygen-Ion-Conducting Membrane (SOM) electrolysis process has been successfully tested on a laboratory scale, producing silicon directly from silica in a cost-effective and environmentally friendly way. A yttria-stabilized zirconia (YSZ) tube, closed at one end was employed to separate the molten salt containing dissolved silica from a liquid metal anode placed inside the YSZ tube. When the applied electric potential between the liquid tin cathode in the molten salt and the anode exceeds the dissociation potential of silica, oxygen ions are pumped out of the molten salt through the YSZ membrane and oxidized at the anode while the silicon cations in the flux are reduced to silicon at the liquid tin cathode. The presence of high-purity silicon crystals on the surface of liquid tin cathode was confirmed by scanning electron microscopy (SEM) and energy dispersive x-ray spectroscopy (EDS). Silicon crystals were extracted from tin cathode by chemical etching.IntroductionPhotovoltaics (PV) generate electrical power by using solar cells, and dramatically reduce the emissions of greenhouse gases (GHG). Through 2006 to 2011, it grew the fastest of all renewable technologies with operating capacity increasing an average of 58% annually [l]. However, the cost of manufacturing solar-grade silicon (SoG-Si) for high-efficiency solar energy production represents a major barrier to achieving the industrial goal for solar power of $1/Wp (watt at peak exposure) which would enable widespread grid parity. The current contract price of silicon to PV manufacturers is $50-$60/kg, with the spot market in 2007-2008 showing prices as high as $300/kg [2]. This makes the development of low cost and environmentally friendly manufacturing of high purity silicon very important."

Jan 1, 2013

By M. Wu, A. Kharicha, J. Bohacek, A. Ludwig

"During the horizontal spin casting of rolls, vibrations and mould deformations seems to have a significant effect on the final quality of the product. Sources for vibrations can be found in the poor roundness and a static imbalance of the chill itself. The bending of the mould axis is also considered. Both, vibrations and axis bending, are used as an input for CFD simulations of the flow dynamics of the liquid metal inside the rotating cylinder. The aim is to study the feedback of the free surface behavior in terms of wave propagation and various wave shapes. Introduction The horizontal spin casting process (HSC) is a casting process that has several advantages over the traditional gravity casting processes. Centrifugally cast products have a high degree of metallurgical purity and homogeneous microstructure. A significant gain is observed for the rupture strength, the rupture strain, and the Young modulus. These properties naturally depend on the centrifugal force and thus, the best mechanical properties can be found at the largest distance from axis of rotation. However proper selection of the angular frequency has to be done in order to prevent the so-called ""metal rain"" i.e. metal droplets can fall down from the upper part of the cylinder due to a too weak centrifugal acceleration. In the same time excessive speeds can lead to the appearance of longitudinal cracks caused by the hoop stress in the initially solidified layer. From empirical knowledge other parameters have important influence on the casting products, it includes the pouring temperature, the pouring rate, the mould coating etc. Recently the presence of natural or forced vibrations have been identified as possible additional factors to be taken into account [1-2]."

Jan 1, 2012