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By Shane Andrews, Gustavo Vasquez, S. K. Varma

"The effect of solutionizing time on the corrosive wear behavior of 2014 aluminum alloy has been studied using the impact and continuous mode of scratching techniques. The transient currents (TC) evolved during the scratching of the alloy shows a linear dependence between the TC and the solutionizing time. Higher TC values at longer solutionizing time may be associated with the changes in the concentration of quenched-in vacancies, grain sizes and dislocations generated during scratching. These factors can either create (a) anodic sites or (b) pitting corrosion resulting in the generation of transient currents. The results have been compared with the similar study carried out for 6061 aluminum alloys. This 6061 aluminum alloy shows similar behavior but the rate of TC generation per unit solutionizing time is much lower than 2014 aluminum alloy. The morphological changes in the impact scratches and the TEM investigation in the scratch have been presented in this paper.IntroductionThe technique of studying corrosive wear of composites of 6061 aluminum in the monolithic and reinforced forms has been reported in the literature [1]. Two modes of scratching, consisting of impact and continuous, in a corrosive environment indicate that the composites, containing 0.10 and 0.20 volume fractions of alumina particles (VFAP), have higher corrosive wear rates than the monolith. A graph between the transient current (TC) generated during the impact scratching as a function of solutionizing time at 540°C indicates linear relationship between them. A similar slopes for the composites were observed and the TC values were less for the composite containing lesser VFAP."

Jan 1, 1998

By Dean G. Heitt

"The Rain and SMZ mines from 1987 to 1994 produced a total of22.0 t of gold from a pre-mine reserve of 14.24 Mt of ore grading 2.13 g/t Au.Gold at Rain is hosted within the basal portion of the Mississippian Webb Formation. ·Mineralization is closely tied to the Rain Fault which is interpreted to be the main feeder for the deposit. Multiple collapse and hydrothermal breccia events provided permeability for the mineralizing fluids in the otherwise unreactive siltstones. Major alteration events include: decalcification and dolomitization of the Devils Gate Limestone; and silicification, baritization, argillization and oxidation of the Webb Fm. Six ore types based on XRD and visual rock chip Jogging have been identified: siliceous ore containing >40% quartz and <30% barite; siliceous-baritic ore containing mostly silica but >30% barite; baritic ore containing >40% barite; argillaceous ore containing >40% total clays (including alunite); calcareous ore containing mostly calcite and dolomite; and carbonaceous ore which has significant pyrite and organic carbon. Metallurgical testing of the oxide leach grade ores found that recoveries, on -1.3 cm crushed material, were greater than 70%. Results also found that Rain ore has strong grind dependency due to silica encapsulation.The Rain leach pad was commissioned in 1988, and to date 9.3·Mt at an average grade of0.65 g/t Au have been placed. Life to date recovery, through December 1995, is approximately 51 %, for a total of3.87 t of gold produced. Two major factors have contributed to the low leach recoveries at Rain when compared with the metallurgical testing: 1) More argillaceous ore than expected was placed on the pad especially late in the mine life and 2) approximately 50% of the tons placed were run-of-mine with no agglomeration."

Jan 1, 1997

By R. K. F. Lam

Unacceptable levels of impurity were noted in high purity chromium melting. Analysis of recent melting data determined that oxygen content in chromium is the critical parameter. Thermodynamics studies identify zirconia to be the most stable oxide in the presence of liquid chromium, followed by alumina and silica. Iron oxide reacts readily with liquid Cr. A certain degree of chemical reaction between liquid chromium and oxides does occur, contamination by the crucible is therefore unavoidable. Equilibrium constants indicate that a chromium oxide addition decreases &apos;ceramic dissolution and reduces impurity contamination. Safe operating conditions with oxygen content between 1190 ppm and 2500 ppm were identified. Additions of chromium oxide (Cr2O3) of 161 grams and 264 grams to liquid chromium yielded acceptable levels of impurity, and oxygen content was respectively increased to 1624 ppm and 2 179 ppm. A new process of melting high purity chromium with chromium oxide addition for controlling the activity of Cr2O3 is recommended.

Jan 1, 1997

By A. D. Neuman, C. C. Davis, M. R. Lopez, A. C. Martinez, T. A. Nothwang, F. G. Hampel, S. L. Voit

"One of the thrust areas for the Global Nuclear Energy Partnership (GNEP) program is the development of actinide bearing fuels for transmutation in a fast reactor. Mixed Oxide (MOX) fuel has an extensive fast reactor irradiation history and thus is being considered for use as a baseline composition from which minor actinides can be incorporated for use as a transmutation fuel. The current study involves characterization of precursor powders and pellets destined for the Advanced Test Reactor in Idaho. These pellets will have three compositions: one standard MOX composition, (U0.80Pu0.20)O1.98, and two compositions of minor actinide mixed oxide (MAMOX) with oxygen to metal ratios (O/M) of (U0.75Pu0.20Am0.03Np0.02)O1.98 and (U0.75Pu0.20Am0.03Np0.02)O1.95. The precursor powders were characterized using a field emission gun scanning electron microscope (FEG-SEM) to determine particle morphology, size, and size distribution. An electron probe microanalyzer (EPMA) was used to characterize element distributions in the pellets.IntroductionThe fundamental purpose of GNEP is to enable a fuel recycling partnership between member nations. The customer nations utilize the fuel for electricity generation provided by and subsequently recycled by the supplier nation. The supplier nation recycles the actinide constituents, mainly uranium and plutonium, in advanced nuclear power reactors, and thus reducing waste volumes [1, 2]. Nuclear materials are strictly controlled through the International Atomic Energy Agency. One of the thrust areas supported by the GNEP program is the development of actinide bearing fuels for transmutation in a fast reactor under the U.S. Advanced Fuel Cycle Initiative (AFCI) in order to transmute long-lived transuranic actinide isotopes into shorter-lived fission products [3].MOX fuel has an extensive fast reactor irradiation history and thus is being considered for use as a baseline composition into which minor actinides can be incorporated for use as a transmutation fuel [4]. Irradiation performance data on oxide fuels with high concentrations of minor actinides is limited, which has prompted this study. This paper discusses the characterization results of precursor powders and pellets prepared for the Advanced Test Reactor in Idaho to determine the effects of including minor actinides in the fuel, and addresses two fuel test matrices proposed by Hilton et al. [3]. The pellets will have three compositions: one standard MOX composition, (U0.80Pu0.20)O1.98, and two compositions of MA-MOX with O/M of (U0.75Pu0.20Am0.03Np0.02)O1.98 and (U0.75Pu0.20Am0.03Np0.02)O1.95. The precursor powders, uranium oxide (depleted, DUO2 and highly enriched, HEUO2), neptunium oxide, NpO2, americium oxide, AmO2, and plutonium oxide, PuO2, were characterized using a FEG-SEM for particle morphology, size, and size distribution. The morphology of the actinide powders was studied in the areas of flowability and porosity in order to predict manufacturability. The MOX pellets were characterized using an EPMA in order to determine impurity levels and locations."

Jan 1, 2008

By H. Y. Sohn

A novel solvent extraction process in which the emulsion is generated by bottom gas injection rather than mechanical stirring has been developed. This process has a number of advantages over the mixer-settler unit or the spray column in terms of simple equipment configuration and the ease of cleaning and process control while providing a large interfacial area for mass transfer. The equipment consists of a horizontal cylindrical vessel in which the two immiscible liquids flow countercurrently. High-strength gas jets are injected from the bottom at certain intervals along the length of the vessel. The gas jet creates a plume zone consisting of an emulsion of the two liquids which contains a large interfacial area for rapid mass transfer. The two liquids then disengage and flow in the opposite directions before entering another plume zone. Thus, the process combines the simplicity of a cylindrical vessel, having no moving parts, with the contacting efficiency of a mixer-settler. The gas can be recycled in a closed loop, thus eliminating mist and other emission problems. These advantages would be especially significant for treating large-volume/low-value liquid streams which contain hazardous substances and/or suspended solid particulates.

Jan 1, 1996

By S. G. Galbraith

We have used the principles of supramolecular chemistry to develop reagents to transport metal salts. These reagents have separated charged "compartments" which recognize a metal cation and its attendant anion(s). They are easy to manufacture as they are structurally related to the commercial hydroxy-oxime extractants for copper. Efficient protocols for loading and stripping of these extractants depend on the novel feature that they bind the metal salt in a zwitterionic form of the ligand. Transfer of the phenolic protons to the pendant amines generates the charged "compartments" to accommodate the metal cation and its attendant anion(s). This paper focuses on how these types of reagent can be used to recover base metals from sulfate and chloride media in flowsheets in which solvent extraction effects separation and concentration operations, interfacing between conventional leach and electrowin/reduction processes. Work on the development of reagents that have high selectivity for metal chloride/sulfate transport, convenient stripping protocols and appropriate hydrolytic stability will be described.

Jan 1, 2003

By Young-Sool Jin, Heung Nam Han, Hong Joon Kim, Jae Kon Lee

A mathematical model was developed considering non-symmetric cooling' and stress distribution in both thickness and width direction of strip on a run-out table of hot strip mill. In order to solve a transient heat transfer equation including the heat evolved from phase transformation, a finite element method coupled with thermodynamic and kinetic analyses was applied. The heat capacity of each phase and heat evolution due to phase transformation were obtained from the thermodynamic analysis of the Fe-C-Mn-Si system based on a sub lattice model. The phase transformation kinetics of the steels was derived by using an inverse additivity technique with continuous cooling experiments. Heat transfer coefficients of strips on the run-out table were, by applying an inverse method, determined from the actual mill data under various cooling conditions. As for the stress analysis, the density change of strip due to cooling and phase transformation, and the transformation superplasticity were considered. A 90nstitutive equation for the transformation superplasticity, which is related to the phase transformation kinetics and the internal stress due to the density change of strip, was applied. A finite element method was adopted to calculate the deformation behaviour of strip on a run-out table of hot strip mill. Using the models, the temperature-phase-deformation history and distribution of a strip on the run-outtable was calculated.

Jan 1, 2001

By Patrick R. Taylor

Glass is used for immobilization of radioactive and hazardous wastes due to its durability and ability to accept a variety of waste constituents into its network structure. Alternative high temperature vitrification techniques have the advantage of increased throughput, increased waste loading and being applicable to variable and heterogeneous waste streams. However, the increased processing temperature places further concerns on the increased volatilization of contaminants, and increased corrosion and erosion of me Iter components. A database of melt properties at higher temperatures, such as partitioning, viscosity, density and electrical conductivity, in the temperature range of 1400-20000 K are being developed.

Jan 1, 2000

By Zhang Chuanfu, Li Shixiong

"In the electrolysis electrodeposition or electroplating of aqueous solution of copper, lead, zinc, nickel, manganese etc, with the increase in cathodic over potential the reducing rate of metal and the cathodic current efficiency increases and the deposit becomes more compact and smooth. According to this principle, a method and equipment of the auto-control of electrolyte quality is invented. The industrial application shows that this method turns the experienced operation into auto-control. The quality and quantity of metal is improved greatly and the consumption of electric energy is reduced.In the electrolysis, electrodeposition or electroplating of aqueous solution of copper, lead, zinc, nickel, manganese etc, usually organic additives are added according to the state of cathodic deposit according to experience. This traditional and experienced operation, often lead to that the quality of additive is not optimum which affects the quality and quantity of metal and increases the consumption of electric energy. To counter the controlling problem of the quantity of additive, the authors have invented a corresponding equipment of the auto-control of electrolyte quality [1], it has found application in industrial practice."

Jan 1, 2000

By Sevinc Yildirim, Cigdem Oruclus

"Metal-Porous Silicon (PS) based structures dipped in water show the direct hydrogen fuel cell behavior. The effect of the thickness of the cupper (Cu) film on the electrical properties of direct hydrogen fuel cell is studied by fabricating Cu/Porous Silicon/n-Silicon/Indium structures. PS samples were produced electrochemical etching of n-type single crystalline silicon with a resistivity of 1,25 Ocm and (111) orientation. The thin films of Cu with different thickness between 200 and 600 nm were deposited on PS surface by electron-beam technique. Investigation of the effect of Cu layer on the performance of the structure indicates that the performance parameters such as open circuit voltage (Voc) and short circuit current (Isc) strongly depend on the Cu layer thickness. It was observed that the divice with an 350 nm Cu layer exhibits the highest open circuit voltage (0,5 V), short circuit current (0,01 mA) and power density (10 W.m-2).IntroductionHydrogen is the most attractive and ultimate candidate for a future fuel and an energy carrier. Hydrogen is recognized as the environmentally desirable clean fuel of the future since it can be used directly in different types of hydrogen fuel cells [1]. In the past years, the rise in portable electronics requires the development of miniature fuel cells compatible with standard silicon micro fabrication technology. Most silicon micro-fuel cells have used the polyperfluo-rosulfonic acid membranes (Nafion R) as a proton exchange membranes (PEM) that is not really integrated with standard micro fabrication techniques [2-5]. The composite materials such as inorganicorganic hybrid materials (Nafion-silica, Nafion-borosiloxane etc) are next generation of proton conducting membrane [4-8]. But, fuel cells run on pure hydrogen gas, which can be produced with other energy resources. Hydrogen smallest atom and thus the H2 gas can leak easiliy. The application of hydrogen for power sources has been greatly restrained due to the lack of safe and convenient generation and storage methods.A kind of hydrogen fuel cells Metal-PS-Si structures used as an energy water directly. There is no need pure hydrogen. Cu-PS-Si Schottky-type fuel cells with as proton-conducting membrane and the thin-film cupper catalist and water as fuel, which are interesting for fabrication of lowcost miniature fuel cells. Generation of the open-circuit voltage and short-circuit current has been observed by Cu-PS-Si structure dipping in different hydrogen-containing solution."

Jan 1, 2014

By Javier Antoñanzas, Susana Caballero, Eduardo Fernández, Jorge Aragón, Juan Carlos Múgica, Lourdes Yurramendi

Air Pollution Control (APC) residues treatment by plasma was studied as a technology for vitrification. During the project a protocol to verify the plasma technology was developed and afterwards applied to a specific case study: the APC residues from Municipal Solid Waste Incinerators (MSWI). Different operational conditions were tested and the vitrified products obtained were analyzed using standardized leaching tests in order to evaluate their new properties concerning safety storage. Two leaching tests were used for the evaluation, the European EN 12457-4 compliance test for leaching of granular waste materials and the French XP X 31-211 test for the determination of the leachability of a solid waste material initially massive or generated by a solidification process. Finally, conclusions about the environmental performances of the technology were obtained.

Jan 1, 2008

By Chao Li, Qian Li, Yong-bin Yang, Kai Li, Qiang Xie, Yuan-yuan Zhu, Dong-ye Li, Qi-bing Tan

"The permeability of sintering mix is a vital technological property in sintering process. However, it can only be measured by off-line method on samples picked from the production. In order to acquire the properties of sintering mix accurately, on-line measuring of permeability is urgently required. Based on the reflection characteristics of bed permeability on pipe flowing parameters, a new method is presented in this paper for on-line measuring of sintering mix permeability. The measurement can be performed by blowing gas flow in the bed with the measuring pipe. Measuring results are obtained by picking the data on flowing rate and pressure in the pipe. The function of flowing rate to pressure may be certain for samples with the same permeability. Thus, the permeability was determined by contrasting this function to the result of off-line measuring, and the relative coefficient or R2 value was more than 99%.IntroductionThe permeability of sintering mix is a vital technological property in sintering process, which directly determines production and quality of sinter, or even determines whether the sinter production is carried out smoothly [1,3].The permeability have more obvious influence on vertical sintering speed, which is mainly related to air quantity passing through material bed. Under certain inducing capacity and negative pressure, the vertical sintering speed mainly depends on the permeability of sintering mix. Low permeability may make burning through point of sintering move back, and the sinter mix cannot be burnt through. High permeability may make burning through point of sintering move forward, improving production efficiency by increasing the speed of sintering machine [4] Good permeability means a small resistance of fan ,reduction of negative pressure of sintering machine, and full contact between air and sulfide, which can strengthen physical-chemical reaction during sintering process and increase desulphurization rate. In gas well through material layer process, gas-solid desulfurization reaction and gas-solid-liquid heat exchange are completed and hot gas through the combustion zone supplies the sintering process with heat. Finally uniform sintering of the material layer in height and width direction is achieved [5] While high permeability index leads to weak sinter strength, fast sintering speed, short residence time of high temperature region and little liquid phase. Moreover, liquid phase in the fast cooling process is too late to fully crystallize but forming glass phase which is harmful to sinter strength as well. Bad permeability means a big fan resistance and increase of negative pressure of sintering machine, which make the air pass through material layer difficultly. When air and mix contact difficultly, removal of sulfide reduces so that desulfurization is incomplete. Meanwhile, low caking efficiency, slow sintering speed and easily burnt sinter , reduce sinter output. Therefore appropriate permeability of sintering mix is the premise of stable burning through point and satisfactory sinter output and quality."

Jan 1, 2013

By Keizo Uematsu, Satoshi Tanaka, Nozomu Uchida, Ronne Hendrajaya

"The influence of microstructural defects on strength in Si3N4 is reviewed. The presence of cracks, pores and inclusions greatly affects the strength of Si3N4. The micron order crack size and distribution were quantified by micrographic technique. The observed defect size was range from 4 µm to 28 µm.The density of defect increases as the defect size decreases. The correlation between defects size and density was better represented on the logarithmic graph. The correlation was linier. IntroductionFracture in ceramics materials occurs from. In order to understand the relationship between strength and defects, it is necessary to examine the fracture process quantitatively.1In this study, the micrographic technique is used to determine the defects size and distribution in Si3N4. The observed data will be used to predict the material strength by using fracture mechanics rnodel.2Experimental ProcedureThe sintered Si3N4 specimens ( SNl, Japan Fine Ceramics Center) were sliced into 1mm thick . The both sides of specimen surface were polished into by using diamond slurries with particle size down to 2µm. The final thickness was 0.045 mm. The optical microscope (NIKON OPTIPHOT02-POL) was used to observed the internal defects with transmission mode. The reflection mode was used to determine the surface defects, so that the internal defect could be distinguished from surface defect. The measurement and counting was taken on the micrograph and the longest part of the defect was measured as the defect size. The size density distribution of internal defect is taken."

Jan 1, 2000

By Henrique Kahn

The Anitapolis alkaline massif in southern Brazil underlies a sub circular area of 6 km2. Bore-hole data show a concentric rock distribution, with mafic rocks in the central part and felsic rocks in the border zone. The rocks are covered by talus and weathered material, 30 m thick on average, and very inhomogeneous in composition. Phosphate mineralization associated mainly with two levels of the weathering mantle and with fresh rocks. A preliminary ore-type classification was based on distribution of apatite, feldspar, vermiculite, biotite-phiogopite, calcite, pyroxene, amphibole and analcime, determined by semiquantitative diffraction method. Technological tests performed on eluvial ore samples from three adits resulted in a subdivision of ore-types based on the difference in behavior due to mineral characteristics during mineral pr

Jan 1, 1991

By Jeffrey Shepherd, Scott R. Smith, Eduard Guerra

"Electrochemical and spectroscopic evidence for the dissolution of a Au electrode by meso-2,3- dimercaptosuccinic acid (DMSA) from an acidic LiCl04 electrolyte is presented. Near the potential of zero charge, DMSA was determined to form a stable layer on the metal surface but at more anodic polarizations, DMSA was displaced from the metal through an oxidative process. The anodic displacement of the layer from the electrode resulted in a small amount of Au that was detected in the electrolyte using atomic absorption analysis. The extent of Au dissolution, was monitored while holding the potential of the electrode for 24 hours at the thermodynamic Eo/H,O in LiCl04 electrolytes containing 10 mM DMSA. This routine resulted in detectable quantities of a soluble Au-DMSA complex in the electrolyte and the greatest leaching was observed at a pH = 2.0. At room temperature, the leaching rate was stable at 10.9 µg cm·2 hr·' however, upon increasing the temperature to 50.0°C, the rate of Au dissolution increased yielding an average rate of extraction of 40.1 µg cm·2 hr- 1. Interestingly, after the first 12 hours of leaching at 50.0°C, the leaching current decreased dramatically suggesting surface passivation which prevented further Au extraction. The implications of this process in the industrial leaching of Au will be discussed.IntroductionThe use of cyanide in the industrial process of leaching Au from ores has raised concerns regarding both operational safety and environmental issues surrounding the disposal of spent leaching eftluents in tailings ponds. Depending on the chemical nature of the processed ore, the spent solutions that are released into the tailings ponds can contain toxic cyanide, either dissolved or complexed with different metals and may pose serious risk to wildlife as well as freshwater contamination to nearby water systems. Because of these issues, some recent studies have focused on the exploration of more environmentally-friendly molecules to selectively leach Au with appropriate kinetics. However, to effectively leach Au into an aqueous solution, a suitable ligand that reacts to form a stable chemical bond with Au is needed to form soluble Au complexes that can be later recovered [I]. Recently several sulfur bearing alternatives have been shown to leach significant quantities of Au in aqueous solutions. These include thiourea [2], thiocyanate [3], and thiosulphate [4]. However, alkylthiols are also known to quickly form a stable covalent Au-S bond [5], but have been relatively understudied in term of their ability to leach Au in solution, even though some short chain thiols are water soluble and relatively nontoxic."

Jan 1, 2012

By Motohiro Horiguchi, Kazuo Ichii, Toshio Oishi

"As a fundamental study to prepare copper-based alloys with rare earths (RE: La, Gd, Nd, Ce and Y) without any inclusions, the solubility of rare earth in liquid copper was experimentally determined. Liquid copper alloys were equilibrated with carbon and rare earth carbide in a graphite crucible in an argon atmosphere at 1523-1873 K.Solubilities of rare earth in liquid copper were determined by approaching the equilibrium values from both the lower and the ·higher concentrations than those expected· in the preliminary experiments. They were expressed as a function of temperature. Carbon in Cu-RE alloy was also analyzed and thermodynamically discussed.IntroductionOver the past several years, the demand for highly conductive and high strength copper-based alloys, such as Cu-Cr, Cu-Zr and Cu-Cr-Zr for use in electronic materials has increased.1 -7 These alloying elements are very reactive and easily oxidized to form oxide inclusions during melting. To avoid the oxide inclusions, it may be effective to utilize the strong reducing power of carbon in conditions under which no carbides form.In this study, to provide fundamental data for producing Cu-RE( rare earth) alloys without any inclusions, the solubility of rare earth in liquid copper in equilibrium with .carbon .was determined and discussed on the basis of the experimental results and the thermodynamic data.ExperimentalSample preparation for equilibrium experimentsOxygen-free copper (99.99%), lanthanum (99.9%), gadolinium (99.9%), neodymium (99.9%), cerium (99.9%) and yttrium (99.9%), and their oxides were used as starting materials.Each rare earth carbide was prepared by mixing rare earth oxide with carbon, which is a little more than the stoichiometric composition, pressing it into a tablet form and sintering at about 2000.K for 20 ks in a vacuum furnace using a graphite crucible. Powder X-ray analysis showed that only the carbon and rare earth carbide (REC2) was present in each sample.Cu-RE mother alloys (5-20 mass % RE) were prepared beforehand by mixing metallic rare earth with oxygen-free copper, and melting in an electric arc furnace."

Jan 1, 2000

By Jiangwei Shen, Cong Wang, Haibin Zuo

The research on the formation of Silico-Ferrite of Calcium and Aluminium (SFCA) in the process of cooling and solidification is rarely reported. The crystallization process was observed by using scanning electron microscopy (SEM) and optical microscope in this paper. The effect of different cooling system on the microstructure and phase composition of the sinters was investigated to obtain the appropriate cooling rate to improve the metallurgical properties of sinters. The experimental results show that the crystallization of calcium ferrite is getting better when the cooling rate is decreased from water quenching to cooling in the air. There are a large number of hematite phases with interconnected crystal structure in the sample cooled in the air. In the case of the compressive strength, it was determined by the mineral composition and pore structure, higher SFCA and hematite contents in sinter cooling in the air lead to a higher strength. Glass phase in the water quenching sinter was the major reason for the lowest strength. High porosity contributes to a decrease in compressive strength for the sinter cooling in the furnace. Therefore the air cooling was the appropriate cooling rate to achieve high quality sinter under this experimental condition.

Jan 1, 2016

By Chen Song

Cobalt basic carbonate particles were precipitated from 1.0mol cobalt nitrate or cobalt sulfate solution with ammonia carbonate. By controlling the zeta-potential of the particles and the ionic strength of the solution, the uniform particles with ellipsoid or rod shapes were obtained. During the precipitation process, the interface tension was diminished to the minimum and therefore the Ostwald ripening and secondary nucleation were both inhibited. The morphology and the size control by zeta-potential seem to be the result of thermodynamics rather than classical crystalline kinetics. The particle sizes were in the range of 0.4-0.6, 0.3-0.4 micrometer. After thermolysis, the spinel-type C0304 particles were produced. The morphologies of C0304 particles were similar to that of their precursors.

Jan 1, 2003

By T. Johnson, B. Q. Li

"Electromagnetic stirring has found a wide application in metals processing for the benefit of obtaining refined solidification microstructures. This paper presents an experimental study on the melt flow and turbulent behavior in an electromagnetically stirred Woods metal pool. The experimental setup consists of metal bath unit equipped with temperature control to allow both cooling and heating, velocity probe positioning unit and data and signal acquisition and processing unit. The whole measuring system is under the control of an IBM personal computer. Velocity measurements are made using the incorporated magnet probes, which are calibrated using a turntable. The measured results showing the effect of the coil positions, coil arrangements and the applied currents on the melt flow are presented. Both mean flow and turbulence quantities are discussed.1. IntroductionElectromagnetic stirring is widely practiced in the metals industry for melt mixing and for casting microstructure refinement. Industrial examples are taken from induction furnaces where the electromagnetic forces are applied to generate desired melt mixing and also various types of electromagnetic stirrers used in various stages of steel and/or aluminum casting processes to produce fine grain solidification microstructure or to eliminate undesired defects such as TCG (twinned-columnar-grain) structure. For ultrahigh purity aluminum or high strength aluminum alloys containing zirconium or lithium, grain refinement can be difficult with the conventional technique, and electromagnetic stirring provides a particularly powerful means to obtain the refined solidification microstructure [1]. A fundamental understanding of the melt flow and the turbulence characteristics in these magnetically-driven flow systems is of significant engineering importance to both process design and product quality improvement.There exists extensive literature on the magnetically-driven melt flows in material processing systems. Nakanish. et al. [2] were perhaps among the early investigators to mathematically and physically model the magnetically-driven flow phenomena in molten metal systems. Subsequent theoretical and experimental work by Tarapore and Evans [3, 4], Szekely and Chang [5], Hunt and Moore [6] and Szekely and El-Kaddah [7] has contributed very significantly to our understanding of magnetically-driven flow in inductively stirred melts. They have developed mathematical models for the electromagnetic field and turbulent flow in induction furnace and validated the models by either laboratory experiments or direct measurements in the industrial-scale induction furnaces."

Jan 1, 1998

By L. Katgerman, H. J. Brinkman, J. Duszczyk

"The phase formation sequence in the in-situ synthesis ofTiB2 in A1 from elemental A1, Ti and B powders is identified with a combination of DSC and XRD. After the melting of A1, A1B2 and A13 Ti are formed at the contact areas between A1-B and A1-Ti. The influence of variations in starting composition on the reaction kinetics is explained in terms of there effect on the different processes in the formation sequence. Parameters in the starting composition that were investigated are; fraction ofTiB2 forming reactants, non stoichiometric Ti:2B ratio's, and addition of alloying element Cu.It was found that a liquid Al phase is necessary for the in-situ TiB2 forming reaction from the intermediate A1B2 and A13 Ti phases. If all Al is consumed by the formation of A1B2 and A13 Ti the TiB2 formation is halted until the decomposition of A1B2 and A13 Ti .Overstoichiometric amounts of B are needed for complete conversion of the Ti, present in A13Ti, into TiB2 This is explained by the fact that some of the stable A1B12 phase is formed after the decomposition of A1B2•The addition of Cu leads to an increasing reaction rate in the A1-Ti reaction. A possible explanation for this is that the A1-Cu liquid penetrates more easily between the Ti and its surface oxide than the unalloyed A1 liquid."

Jan 1, 1998