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By N. El-Kaddah, J. W. McKelliget

"A mathematical model for the analysis and design of hybrid plasma reactors for advanced materials synthesis is presented. The model is based upon a solution of the electromagnetic vector potential equation and is capable of predicting the two-dimensional velocity, temperature, and electromagnetic fields as well as the reaction kinetics inside the reactor for any axi-symmetric coil configuration. The model is used as a computer aided design tool for the design of hybrid plasma reactors consisting of a conventional DC torch augmented by an RF induction coil and it is demonstrated that the hybrid system possesses superior characteristics for materials synthesis over conventional DC or RF systems. The coupling between the RF and DC components is found to affect both the temperature field and the flow field and to have a significant effect on the reaction kinetics and on materials recovery. The model is used to study the thermal decomposition of silicon tetrachloride as a function of reactor design and operating parameters and it is demonstrated that through a CAD approach it is possible to significantly improve the operation of materials synthesis systems.IntroductionIn recent years there has been growing interest in the use of the inductively coupled plasma for chemical synthesis as a way of meeting the increasing demand for high quality, high performance materials for use in critical applications/l/. Although the basic feasibility of this approach has been demonstrated in the laboratory/2,3/ there still exists a number of operational problems that adversely affect system performance for some applications. In particular, the recirculation and back flow effects that arise from the electromagnetic forces in the plasma can result in the repulsion of the reactants from the hot plasma core and their subsequent deposition on the walls of the reactor. Another operational problem arises from the fact that the energy dissipated in the plasma has to compensate for the heat losses to the environment by conduction, convection, and radiation in order to maintain the ionization of the plasma and, hence, the stability of the plasma may be affected by the presence of the reactants and their products."

Jan 1, 1988

By J. P. Downey, L. G. Twidwell

"The high density sludge process (HDS) is a commercially proven acid rock drainage wastewater treatment process that is based on acid neutralization and metal precipitation. Previous studies have established that metal removal efficiencies in precipitation-based wastewater treatment applications can be improved through metal ion adsorption on ferrihydrite and/or aluminummodified ferrihydrite. This study was conducted specifically to determine whether the metals removal efficiencies at an existing industrial facility could be improved by promoting ferrihydrite and/or aluminum-modified ferrihydrite precipitation during the pH adjustment stages of the HDS process. The metal tenors of the treated wastewater samples are compared with those obtained through baseline experiments, which were designed to simulate the conventional HDS operation. The subject metals were: aluminum, arsenic, cadmium, copper, iron, manganese, nickel, and zinc.IntroductionThe HDS process is commercially proven ARD wastewater treatment technology that involves raising the wastewater pH by adding hydrated lime, caustic soda, or another alkaline substance. In addition to neutralizing the acidity, many dissolved metals precipitate as pH is elevated. Waste volume is minimized by capturing and immobilizing the precipitated solids.However, ARD streams characteristically contain multiple dissolved metal species. The response of various metals to pH adjustment in the HDS process is neither uniform nor quantitative, so minor to trace concentrations typically remain in the treated wastewater following solid-liquid separation. The effectiveness and applicability of the process would be improved if a means were found to further reduce the metal concentrations.Previous research and industrial applications have proven that metal ion adsorption on ferrihydrite (FH) and/or aluminum-modified ferrihydrite (AMF) increase metal removal efficiencies. Ferrihydrite and AMF are considered ideal for cation and anion adsorption from an aqueous solution at the appropriate pH [1]. Ferrihydrate adsorption of dissolved heavy metals is widely practiced throughout the world [2, 3]. It is established that FH and AMF effectively adsorb As contained in aqueous solutions [4]. Arsenic removal by adsorption on FH is the U.S. Environmental Protection Agency’s (EPA) Best Demonstrated Available Technology [5]. Twidwell and Leonhard also demonstrated that heavy metals (Cd, Cu, Ni, and Zn) are effectively removed from solution by coprecipitation/adsorption using AMF and FH [6]."

Jan 1, 2008

By Guo-hua Bai, Hong-jing Yuan, Qian Li, Yong-bin Yang, Tao Jiang, Yan Zhang

"The effect of different additives on the bio-oxidation of arsenic-bearing gold ores has been carried out to solve the problems such as long period of leaching, low oxidation rate. The oxidants strengthen the cathodic reaction and thus improve the leaching rate by the increase of electron transfer. Meanwhile, silver catalysis is also effective for the decomposition of arsenicbearing gold ores due to the strengthening of anode reaction. Co-intensification by oxidants and Ag (I) is more efficient to the bio-leaching and the conversion of As (III) because the anode and cathodic reaction of biological oxidation of sulphide ores were both strengthened. The leaching rate reached to 63.94% after bio-leaching 13days by co-intensification of Ag (I) and Fe(III).IntroductionWith the worsening global ecological problems and the gradual exhaustion of available gold resources, metallurgical technology of refractory gold ore has received more and more attention and become possible due to its good advantage of the economic effects and negative effects to the environment. Refractory gold ore, the direct cyanide leaching rate of that is defined as less than 70%, has become an important raw material in gold extraction industry, in which sulfide bearing gold ore represents a large proportion, pyrite and arsenopyrite (FeAsS) is a common gold-bearing mineral. Since the gold is often encapsulated in the crystal lattice of these minerals, destruction or alteration of the ore to liberate the submicron and/or structurally bond gold is necessary[l]. Even if the ultrafine grinding approach also is generally not sufficient for these refractory ores and additional techniques like roasting, pressure oxidation and bacterial oxidation are used to liberate the gold [2]. In the three pretreatment processes, bacterial oxidation is characterized by its new ideas, low cost, no pollution, simple equipment and operation, high leaching index and become the most promising process which has received much attention over time [3-5]. But its further application is limited by some of its own shortcomings, such as long pretreatment time and the toxic effects of arsenic to bacteria on bio-leaching limit."

Jan 1, 2013

By W. C. Chang

Phases and magnetic evolutions of melt spun Nd9.5(Fe1-xCox)85.5B5 (x=0, 0.05, 0.1 and 0.15), (Nd1-yLay)9.5Fe85.5B5 (y=0, 0.0.5, 0.1; and 0.15) and (Nd0.95La0.05)9.5(Fe1-zCrz)81.5B9 (z=0, 0.033, 0.067 and 0.1) nanocomposites: have been investigated. It was found that a. dilute Co substitution for Fe, x=0:05-0:15, in Nd9.5(Fe1-xCox) 85.5B5 improved not only Curie temperature but also the remanence and maximum energy product. Partial substitution of La for Nd in(Nd1-yLay)9.5Fe85.5B5 may suppress the grain growth of the materials during thermal treatment. Exchange coupling between the Nd2Fe14B and a-Fe was found: to increase with increasing La content. A dilute La-substitution, y=O. 10, has proven to decrease the optimum wheel speed required for preparing melt spun ribbons with better magnetic properties; Furthermore; a slight substitution of La for Nd in (Nd0.95La0.05)9.5(Fe1-xCrx)81.5B9 nanocomposite reduced the crystallization temperature of the over-quenched ribbons and led to the formation of a multiple phases mixture. Nevertheless, a dilute Cr addition increases the Tg of (Nd0.95La0.05)9.5(Fe1zCrz)81.5B9 and also suppresses the formation of the undesired (Nd,La)2Fe23B3 and Fe3B phases: Cr was found to play an important role in grain smoothening or magnetic separation which consequently increased the Hc of Cr-containing materials.

Jan 1, 1997

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

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

Jan 1, 2011

By Robert W. Bartlett, Keith A. Prisbrey

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

Jan 1, 1997

By P. Wieser, D. Feke

"Priming of filters with small pores is influenced by the surface tension of the liquid metal and may be complicated by freezing • Freezing followed by melting has been observed experimentally. This process has been modeled on the basis of one dimensional heat flow by radiation to the filter and by conduction in the metal. Also considered are super-heat of the metal and the initial filter temperature. The results of the model provide useful guidelines for the application of filters. IntroductionFiltration has been recognized as a valuable method of refining by removing suspended phases from liquid metals or alloys. Woven fiberglass type fabrics and wire screens were used initially in the aluminum industry. With the introduction of the ceramic filters that exhibit improved inertness and refractoryness, filtration has been introduced to higher melting alloys including cast irons, superalloys, stainless steels, as well as low and medium carbon low alloy steels. A considerable literature is delveloping rapidly on the progress in applications and the advances in understanding the mechanisms and effectiveness of filtration processes (1-8).With the use of filtration for different alloy systems for the production of cast to shape parts a bewildering variety of gating system modifications has been developed (Figure 1) to accommodate the installation of filters in the mold. The modifications have two principal purposes: 1) the runner expansion is intended to compensate for the resistance to flow due to the filter and that of the captured inclusions, and 2) the metal reservoir upstream of the filter, provides a temporary by-pass which permits metal to flow across the filter and heat it until priming can be accomplished. priming of.filters by low and medium carbon steel is readily accomplished but, compared to such alloys as cast iron or 19 Cr-9Ni stainless steel, requires greater precautions to avoid failure to prime by excessive freezing on or inside the filter pores. This problem is further examined below:"

Jan 1, 1986

By Takashi Miyamoto, Hideo Nakae, Hideki Yamaura, Takeshi Yanagihara

"For the production of partially composed metal matrix composites, namely discontinuous MMCs, using a casting· process, the interpenetrated phase composites with SiC particles were fabricated by pressureless iDfiltration using molten Al-Si alloys. This process is based on a wetting phenomenon, therefore, we discussed the technique based on the reactive wetting. The SiC particles coated by diluted water glass were sintered in a mullite Tammann tube and simultaneously infiltrated with molten Al-Si alloys in air at 1173~1573K. As for the improvement of the wettability between the SiC and the liquid aluminum alloy, Fe3O 4 powder was mixed with the water glass due to the thermit reaction between Fe3O4 and molten aluminum alloy. In some experiments, pure aluminum powder was placed on the sintered SiC to increase the interfacial area and the chemical reaction between the sintered Sic. and the melt. By combining these conditions, we succeeded in the complete infiltration without pressure at 1173K.IntroductionAs is well known, the mechanical properties of metal matrix composites (abbreviated MMCs) are superior than that of ordinary metals. However, their use has not been widely accepted because the production cost is very high due to their poor machinability. Therefore, the production of partially composed, namely discontinuous MMCs, by as the Lanxide process [l,2] has been investigated for many years. The Lanxide process, it takes a long time, sometimes up to 10h, in a nitrogen atmosphere for the infiltration. Therefore, the cost will be higher for common use. On the other hand, a high 'pressure process has been adopted for the production of discontinuous MMCs by the Toyota Motor Corp.[3]."

Jan 1, 2000

By Yan Fu, Chuanlin Fan, Xiujing Zhai, Yongfeng Chang, Binchuan Li

"The mechanism of the selective chlorination of nickel and cobalt in reduced limonitic laterite was investigated. Reduced ores were obtained from the reduction roasting of a limonitic nickel laterite. The thermal decomposition of related chlorides and the selective chlorination of the reduced ore were carefully studied using Differential Thermal analysis - Thermogravimetry (DTA-TG), X-Ray Diffraction and chemical leaching methods. In the temperature range of 300 - 500 °C, aluminum chloride hexahydrate was chosen as chloride agent. During the selective chlorination, reduced ore was partly chlorinated by hydrogen chloride generated from the thermal decomposition of chloride agent. Then the oxydrolysis of ferrous chloride re-generated hydrogen chloride was used to further the chlorination. Finally, iron was mostly rejected as hematite, while nickel and cobalt were selectively chlorinated. More than 91 %Ni , 90%Co and about 4%Fe in the chlorinated ore was extracted using a water leaching method.IntroductionLimonitic nickel laterite is an important nickel reserve, which is rich in iron in the form of goethite and has low contents of magnesium, aluminum, silicon, and other elements. Goethite is the main nickel-bearing mineral in the laterite [1]. Nickel is generally present in goethite in three modes: (a) associated with amorphous or poorly crystalline goethite, (b) weakly adsorbed to the crystalline goethite surface, and ( c) as lattice substituents [2]. In addition, cobalt in limonite was found to be associated with a manganese phase rich also in nickel [3]. These results indicate that the extractions of nickel and cobalt are highly dependent upon the degree of the decomposition of the nickel, cobalt-bearing minerals.For the selective extraction of nickel and cobalt from limonitic laterite, the ore is usually processed by hydrometallurgical methods, including high pressure acid leaching (HPAL) [4] or reductive roasting - ammonia leaching (Caron process). However, there are still some disadvantages in these processes, such as the expense of autoclaves and scaling problems in HP AL [ 4, 5], and relatively low overall metal recovery, large energy and reagent requirements for the Caron process."

Jan 1, 2011

By Maura Malone, Neil Gao, Daniel Liu

"Corrosion is the primary failure mode for aluminum cathode sheets used in Teck's Trail Operations electrolytic zinc plant. It was observed that the corrosion performance of Al cathodes from different suppliers varied considerably. This suggests that the material properties of Al cathodes have a strong influence on corrosion resistance. In the current study, various types of Al alloys, including 1050, 1060, 1070, HIS and 1090, were characterized through chemical analysis, corrosion testing, mechanical testing and metallography. The results are discussed with a focus on the effects of impurity elements and second phase particles on corrosion resistance. The findings were used to improve the Al cathode sheet specification and to develop a standardized screening procedure which details qualification steps for comprehensive evaluation prior to a plant trial.IntroductionAluminum (Al) cathode replacement is a major operating expense at Teck's Trail Operations zinc electrolytic plant. Currently, approximately 0.5% of daily stripped Al cathodes are removed from service because of failures caused mainly by corrosion. Edge corrosion and acid (solution) line corrosion are the most severe types of corrosion, resulting in more than 50% of cathode failures.Corrosion of Al cathodes has been intensively investigated for over two decades and the origins and mechanisms of Al cathode corrosion are well understood [1-4]. Halide anions contained in the electrolyte are the primary culprits for the corrosion and sticking problems of Al cathodes. Both fluoride (F') and chloride (Cl"") result in localized passivity breakdown on the surface of the Al cathode, causing pitting corrosion. Bouarzaiga investigated the corrosion of Al cathode samples partially immersed in electrolyte and found that the formation of Ch at the electrolyte/air interface was the primary contributor to solution line corrosion [2]. Because of the significant impact of F"" and Cl"" on Al cathode corrosion, it is imperative to maintain these concentrations as low as possible in the electrolyte."

Jan 1, 2012

By Line Hallgren

The fluid flow in the mold during up-hill teeming is of great importance for the quality of the cast ingot and therefore the quality of the final steel products. At the early stage of the filling of an up-hill teeming mold, steel enters, with high velocity, through the nozzle into the mold and the turbulence on the meniscus could lead to entrainment of mold flux. The entrained mold flux might subsequently end up as defects in the final product. It is therefore very important to get a mild and stable inlet flow in the entrance region of the mold. It has been acknowledged recently that swirling motion induced using a twist tape swirl blade, in the submerged entry nozzle is remarkably effective to control the fluid flow pattern in both the slab and billet type continuous casting molds, resulting in increased productivity and quality of the produced steel. From the above result, we propose, swirling flow generated through a swirl blade inserted into the entry nozzle, as a new method of reducing the deformation of the rising surface and the unevenness of the flow during filling of the up-hill teeming mold. The swirling blade has two features: (1) to generate a swirling flow in the entrance nozzle and (2) to suppress the uneven flow, generated/developed after flowing through the elbow. The effect of the use of a twist tape swirl blade was studied using both numerical calculations and physical modeling. Water modeling was used to assert the effect of the swirling blade on rectifying of tangential and axial velocities in the filling tube for the up-hill teeming and also to verify the results from the numerical calculations.

Jan 1, 2006

By Carlos A. Ferreira, Betina Hansen, Marco A. S. Rodrigues, Marcela P. Proença

"Nowadays, the concern with the reduction of industrial pollution has motivated researchers to found out new technologies for treatment of industrial waste. The clean technologies, as electrodialysis, are capable of treating these residues, minimizing the impacts when they are discarded directly on the environment. Membranes of SPS/HIPS, PAniCSA/SPS/HIPS, SPAN/SPS/HIPS were developed using chemical mixture method. Membranes were characterized by Infrared Spectroscopy (FTIR), Thermogravimetric Analysis (TGA), Dynamic Mechanical Analysis (DMA) and Scanning Electronic Microscopy (SEM). Membranes were submitted to electrical polarization and to electrodialysis at NaCl and KCl solutions, in order to determine ionic transport through the membranes. Results were compared with commercial membranes. The average percent extraction for Na+ ions obtained by membrane was beyond 20%.IntroductionThe high environmental impact caused by the galvanoplastic industries represents today a world concern(1). In the galvanoplasty, thin metallic layers are deposited on metallic surfaces(2) through chemical methods or electrochemical process. This industrial process presents some disadvantages that limit its utilization, as the generation of toxic effluents containing concentrations of heavy metals usually above the limits allowed for his release in receiving bodies(1), the production of galvanic sludge which is considered hazardous waste and that is very difficult to treat, beyond the high consumption of water (3).Stimulated by the development of new ion-exchanged membranes with high selectivity, lower electrical resistance, and improved thermal, chemical and mechanical properties, the use of electrodialysis in the wastewater treatment has recently gained a broader interest(5). The electrodialysis (ED) is a mass separation process in which electrically charged membranes and an electrical potential difference are used to separate ionic species from an aqueous solution(5). The technique permits the recovery and the reutilization of the waste products from the industrial process, avoiding the discharge of them on the environmental (acting as clean technology)."

Jan 1, 2008

By Camila Martini Matos, Maria das Graças da Silva Valenzuela, Francisco Rolando Valenzuela Diaz, Lucy Gomes de Sant' Anna, Orley de Oliveira Magalhães, Flavio M. S. Carvalho, Isaac Jamil Sayeg

"Kaolin clays are widely used in various industry segments. Its main properties are fine granulometry, chemical inertness and whiteness. In general, kaolins are not easily organophiilized as a result of its 1: 1 structure. The aim of this paper is to describe the modification of a Brazilian kaolin sample, in order to obtain an organophilic kaolin of high performance. The clay as received was identified by X-ray diffraction and characterized by optical microscopy, cation exchange capacity and swelling tests for observation of their performance in water and organic solvents. Then, the sample was treated with a 10% sodium carbonate solution and with ammonium quaternary, washed several times with distilled water, dried at 60°C, and characterized by XRD and swelling assays. Our results show that the clay was organophiilized and its ability to swell in organic solvents has increased.IntroductionThe kaolin clay, also known as ""china clay"" is chemically a hydrated aluminum silicate characterized as a very fine powder and lamellar structure (1:1), being constituted mainly by kaolinite [l]. Kaolin is a mineral extremely used as raw material. Its properties such as color, softness, small particle size and chemical inertness make it a suitable material for several industrial applications. The desired properties of kaolin varies widely for each application, beginning with its largest use in the paper industry until minor uses in the sectors of cosmetics and pharmaceutics. These two last applications require purified kaolin with defined functionality [2]. To find improvements in the functionality of kaolin for specific applications is important for many industrial uses. Sometimes the way to find these improvements might be modification of the kaolin clay by treatment with a chemical substance as ammonium quaternary, causing surface modifications [3,4]. In this work is described the modification of a Brazilian kaolin sample by treatment with cetyl trimethylammonium chloride (CTAC). The properties of the modified kaolin are being assessed by characterization and essays to understand its functionality and industrial application."

Jan 1, 2013

By Thomas Brynjulfsen, Merete Tangstad

"Manganese ore fines, generated during mining and transportation, can not be added to the submerged arc furnace directly as they will prevent even gas flow through the burden. Low gas permeability in the burden will lower the degree of pre-reduction of ore and subsequently increase the carbon and energy consumption of the process. In order to utilize manganese ore fines in the furnace they are agglomerated into sinter, pellet or briquettes. The agglomeration process will however change the reduction properties of the ore. In this work the melting and reduction properties of sinter has been investigated.The melting temperature and melting mechanisms has been studied. The mineralogy of the raw ores and agglomerated has been found using XRD, and the composition established using EPMA(WDS). The effect of adding fluxes such as dolomite and quartz has also been investigated.IntroductionManganese metal is produced in a submerged electric arc furnace or in blast furnaces. The reduction of manganese oxide in blast furnace has in the recent years become more unusual due to the high consumption of reducing carbon material[5]. Manganese metal for alloying in steel usually contains silicon and iron, and are therefore called ferro manganese and silicomanganese.During mining, transportation and handling the manganese ore is broken up into different size fractions. The larger lump are used directly in the electric arc furnace, but the finer materials can not be added without treatment. The fine ore can disrupt the flow of CO and CO2 gas through the burden, subsequently reducing the degree of pre-reduction. The fine fractions must therefore be agglomerated into larger lumps, in order to promote gas flow. This can be achieved through a number of different processes. The agglomerate used in this work has been sintered, which means that is has been partly molten and reduced, in order to create bigger lumps."

Jan 1, 2012

By G. Gomathi, K. Asokan, K. Subramanian

An electrochemical reactor with anode and cathode chambers separated by a composite perfluoro polymer cation exchange membrane was designed, fabricated and used for the reduction of dissolved carbon dioxide under ambient conditions to formate. The flow reactor enhanced the mass transfer of carbon dioxide compared to the batch reactor. Experiments were conducted using two different perfluoro polymer membranes - Nafion 961. Efficacy of CO2 reduction on various cathode materials (Cd, Pb, Sn and Zn plated stainless steel woven mesh) were determined. Optimum values of flow rate and current density were evaluated for the energy efficient formation of formate in aqueous KHCO3 (pH 7.5-8.5) buffer solutions.

Jan 1, 2008

By A. E. Clark

Rare earth compounds are widely known as possessing many extraordinary magnetic properties. In this paper, we focus on the huge magnetically induced displacements (magnetostrictions) which characterize the compounds of terbium with iron (Terfenol). Materials prepared commercially by both free-standing-zone (FSZ) and modified Bridgman (MB) techniques have now become available in large sizes and shapes. Prior to the development of the Terfenol alloys, it was possible to achieve giant magnetostrictions only at cryogenic temperatures. In the cubic Laves phase TbFe2 compound, saturation strains exceed 3000 x 10-6 at room temperature and above. Large magnetization 'jumps' can occur, causing huge spontaneous magnetostrictions with small triggering magnetic fields.

Jan 1, 1992

By Huaming Yang

The vanadium-doped SnO2 nanoparticle was synthesized by the co-precipitation reaction and subsequent calcination from the vanadium(III) chloride and tin(IV) chloride. The crystal size, pore size distribution, micrograph and properties of the nanocrystalline powders were examined by differential thermal analysis (DTA). thermogravimetric analysis (TGA). X-ray diffraction (XRD), desorption isotherm (Barrett-Joyner-Halenda method) and transmission electron microscopy (TEM). Thermal treatment of the precipitate powder at 600'C led to the formation of crystal0nmincrystal size. Most of the pores in the narmparticle are about 5~15nm in diameter. Effect of doped vanadium on the crystal size of the nanoparticle was discussed.

Jan 1, 2003

By Seong-Jong Kim

The formation behavior and corrosion characteristics of anodic oxide films on pure Mg and Mg-AI alloys were investigated focusing on the effects of anodizing potential, Al content, temperature and NaOH concentration. Pure Mg and Mg-AI alloys were anodized for 10 min at 3, 10, 40, and 80 V in NaOH solutions. Mg(OH)2 was generated by an active dissolution reaction at the surface of the specimen and the product was affected by temperature while MgO generation increased with NaOH concentration. Moreover, the current density after anodizing for 10 min at a constant potential decreased with increasing AI content in Mg-AI alloys,

Jan 1, 2003

By P. A. Davidson, D. J. Short

"In this paper we describe a 'non-contact' electromagnetic nozzle suitable for sprayforming and gas atomization processes. In such processes there is a need to control the flow rate and diameter of the liquid metal jet whilst minimising contamination of the stream. This can be achieved using an electromagnetic valve, which partially levitates the jet in freespace, using a segmented cylinder surrounded by an induction coil. This valve will significantly enhance the quality of the titanium alloys and nickel-based superalloys used in sprayforming and gas atomization. This paper describes the design and test of a laboratory prototype valve based on experiments performed with liquid tin.1. Introduction In many industries there is an increasing need for clean, high quality metals and alloys based on titanium and nickel. Two important processes are: 1) Spray deposition which allows the liquid metal to be converted to a near-net shape, thus alleviating the need for subsequent forging and extensive machining and; 2) Powder production of titanium by gas atomisation.In centrifugal spray deposition of titanium (see figure 1) the metal is induction melted in a cold crucible. The crucible consists of a number of water-cooled segments, which allows the high frequency magnetic field of the coil to pass through the crucible, and into the melt. The charge is melted by the induced eddy currents. Locally at the crucible walls the liquid metal solidifies, and is contained within a. 'skull' of its own solid, thus reducing contamination from the crucible wall. Once melted the metal is poured through an electrically heated graphite nozzle and into the spray forming chamber. The principal limitation of the process to-date, however, is that it currently uses a graphite and /or ceramic nozzle to direct the flow of liquid metal to the atomizing disk and as such there is considerable risk of nozzle erosion with inevitable effects in terms of contamination of the melt stream and variability in flow conditions. In this research programme we develop a. non-contact electromagnetic nozzle, which will totally eliminate refractories and/or ceramic materials from the melting and casting process. This will greatly enhance the technological capabilities of sprayforming and gas atomization processes."

Jan 1, 1999

By Shengqin Zhang, Jagannath Pal, Yousef Mohassab, Hong Yong Sohn, Mohamed Elzohiery

The kinetics of magnetite reduction with mixtures of hydrogen and CO of various compositions has been investigated as part of the development of a flash ironmaking process at the University of Utah. This new process bypasses the cokemaking and pelletization or sintering steps required for the blast furnace. The particle kinetics were studied using magnetite concentrate particles of different sizes. Reduction degree of 60% was achieved in a few seconds in at 1350 oC using CO reductant alone and over 90% when H2 + CO gas mixture was used. The effects of reductant partial pressures, temperature, and particle size on the reduction kinetics were studied.

Jan 1, 2016