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By Rodney L. LeRoy, Michel G. Drouet, Peter G. Tsantrizos

"DROSRITE is a unique process that makes possible economic in-plant recovery of metal from hot aluminum dross. It is environmentally friendly, requiring no salt and producing no C02 or NOx gases. The salt-free residues of the process are suitable for production of calcium aluminate or for other value-added use. The process is highly energy efficient, extracting process heat from energy in the residue and, thus, it does not require an external plasma torch, electric arc or fuel heat source.A DROSRITE pilot unit built by PyroGenesis has been tested with both black and white dross types. The unit was installed at two different aluminum plant locations, and tests were conducted for a total of six weeks ""online"" with hot metal holding furnaces where the dross was skimmed.Results of both of these industrial trials are presented, together with an economic analysis indicating cost savings in excess of $1 70 per ton of dross treated."

Jan 1, 2000

By T. Ikeda, M. Maeda, K. Mita

Galvanized steel sheet is the major product for the automobile industry. Therefore, automotive recycling results in zinc-containing scrap that should be remelted in EAFs. Naturally, the EAF dust is a very important source of zinc for zinc recycling processes. The thermodynamic properties of the Fe-Zn intermetallic compounds formed on the surface of galvanized steel sheet should be clarified to make clear the evaporation mechanism of zinc; however, there are few reports on these compounds because of difficulties in their synthesis. There are various intermetallic compounds in the Fe-Zn system. We synthesized them at about 673K. A specimen was examined chemically and X-ray diffraction was applied to ensure the formation of intermetallic compounds. Material containing two phases was placed in a Knudsen type effusion cell and the mass spectrum studied to evaluate the vapor pressure of zinc. The thermodynamic property of intermetallics was then evaluated through measured intensity.

Jan 1, 2000

By Manolete Mena

WC-Co nanocomposite powder is among the first group of materials with a promising potential for nanocrystalline-materials application. A chemical vapor synthesis (CVS) process that has previously been used for preparing the aluminides of titanium and nickel, and other metallic and intermetallic powders has been applied to the preparation of WC-Co nanocomposite powder. This CVS system was designed so that a tungsten precursor (WCl6 powder) and a cobalt precursor (CoCl2 powder) were separately fed into each evaporator in a reactor by means of specially designed powder feeders. The reduction and carburization of the vaporized chlorides by methane-hydrogen mixtures produced nanosized WC and Co composite powder. The product is a very uniform mixture of the constituent powders, which is important to ensure a high quality of the bulk cemented tungsten carbide product after consolidation. In the present work, the effects of reaction temperature, CH4 to WCl6 ratio, CH4 to H2 ratio, residence time, and Co content on the powder composition and particle size were determined. The products were characterized using XRD, carbon analyzer, and TEM.

Jan 1, 2006

By J. Pérez

A lead smelter slag with high copper, lead, arsenic and silver contents was treated at laboratory scale for arsenic removal. The slag was first leached at atmospberic pressure with sulfuric acid and oxygen. According to arsenic contents leaching of most of the arsenic was achieved in either one or two stages, producing a lead-silver rich residue and a solution high in copper and arsenic concentrations. Alternative routes were considered to treat the resulting solution. Firstly, solvent extraction of arsenic with a mixture of TBP and 2-etbyl-bexanol was tested and extractions of over 95 percent of arsenic were achieved. Secondly, a copper arsenate precipitation treatment was done to eliminate arsenic and copper from solution.

Jan 1, 1996

By KNona C. Liddell

"Many metal recovery processes involve heterogeneous reactions in porous media accompanied by fluid flow and mass transfer. Modeling such systems is difficult because of the number of rate processes involved and is complicated even further by effects due to the structure of the porous medium. Data on even bulk properties of the medium are often severely limited or unavailable. For many such systems, a cell model may provide an attractive alternative to models based on transport mechanisms in a differential volume. A cell model requires less input data and is computationally efficient. Identical residence time distributions can be obtained with models of both types, and both allow conversion and concentration profiles and histories to be calculated. The formulation and properties of cell models for metals recovery are described in detail.INTRODUCTIONSubsurface mineral leaching, metal ion recovery and environmental remediation are significant modeling challenges. They involve one-, two-, or three-dimensional reactive flow in multi reaction open systems. Dissolution, adsorption, and ion exchange occur at reactive mineral surfaces, and these heterogeneous reactions are accompanied by acid-base, complexation, and redox reactions in the solution phase.Two approaches have been taken to reactive flow problems in geologic media: mixing cell and transport models. Mixing cell models, the subject of this review, are based on a network of connected cells, each with a specified number of input and output streams. Mixing cells are assumed to have no internal solute concentration gradients, that is, each cell behaves like a well-stirred tank. Gradients are represented by step changes between connected cells; this results in a model that is spatially discretized at the outset. Different methods of discretizing the model equations are considered more fully below. Although this is not strictly necessary, it has usually been assumed in subsurface flow applications that all cells in the network have the same volume and identical initial properties."

Jan 1, 1996

By T. Kozuka, K. Sassa, S. Asai

"A new atomization process is developed. The principle of this process is completely different from that of conventional processes. This process uses electromagnetic energy induced by direct electric current and direct magnetic field instead of kinetic energy produced by fluid impingement or disk rotation.Experimental work of this process was carried out using pure tin, and it was found that the crucial factor for a stable operation is the contact state of molten metal with the electrode. In order to control the condition, a delay time controlling unit was developed and combined with this process. It is noticed that this controller works well to produce uniformly sized particles.A linear relation between the impulse and the momentum of atomized particles is found by use of experimental data and is explained by theoretical analysis.IntroductionIn atomization processes prevailing in metal powder technology, kinetic energy is currently employed for atomizing molten metal. That is, molten metal is broken into small particles by other fluid (e.g. water, argon gas, etc) or by impinged upon a rotating solid disk. This splashing process is always accompanied with uncertain factors for shape and size of the particles. The diameter distribution of products, therefore, comparatively spreads over a wide range. From another standpoint, the restriction of atmosphere is inevitable in some of these processes. As a pulverizing technology, the process which can produce uniformly sized particles and permits the choice of atmosphere is strongly desired.On the other hand, a great attention has been paid to the spray casting process as a new near net shape casting. In this process, a small size spraying device is favorable."

Jan 1, 1988

By Kejun Liu

Platinum and palladium are usually dissolved together and followed by separation. In this study, the selective leaching of platinum and palladium from a secondary resource, such as dental waste, by using chloride solution (hypochlorite and chlorate) has been developed. Results indicate that about 100% of palladium could be initially extracted by the combination of 0.3 mol/L sodium hypochlorite (NaClO) and 0.068 mol/L sodium chloride (NaCl) at pH 1.2 and 298K in 1.5 hours, or the combination of 0.005 mol/L sodium chlorate (NaClO3) and 6 mol/L hydrochloric acid (HCl) at 298K in 0.5 hour. About 100% of platinum could be extracted from the residue by the combination of 0.47 mol/L sodium chlorate (NaClO3) and 12 mol/L hydrochloric acid (HCl) at 298K in 2 hours.

Jan 1, 2003

By F. H. (Sam) Froes, C. Suryanarayana, K. C. Russell, C. M. Ward-Close

"Far from equilibrium synthesis allows development of novel crystal structures and microstructures, leading to achievement of enhanced physical and mechanical properties. A number of ""far from equilibrium"" techniques are reviewed with emphasis on the amount of departure from equilibrium. The ability of two such techniques, mechanical alloying (MAl, and physical vapor deposition (PVD) to develop novel structures are discussed in detail. For the MA process emphasis is placed on intermetallic compound compositions. Solubility extension, beyond rapid solidification (RS) levels, is found in terminal compositions but not for the intermetallics. Nanostructure-sized grains (< 100nm) form which can be retained after ""low temperature"" compaction. On continued milling in many cases the nanometer-sized grains transform to an amorphous structure. Ordering is destroyed by MA, except in those intermetallics with large negative enthalpies of formation. For the PVD process, a review of application to terminal light alloy compositions is presented. This includes a new high-temperature aluminum alloy, layered materials with nanometer spacing, corrosion-resistant magnesium alloys and low-density titanium compositions. IntroductionTo enhance the mechanical property combinations of advanced structural materials innovations in process/synthesis are required [1-6]. In this paper the capability of various ""far from equilibrium"" synthesis techniques [7,8] to produce novel constitutional and microstructural effects, and hence potentially enhanced physical and mechanical properties, in advanced materials is presented. The application of two such methods, mechanical alloying (MA) and physical vapor deposition (PVD) is discussed in detail. For the MA process emphasis is on intermetallic compositions with consideration given to solid solubility extension, microstructural refinement, amorphization, and formation of intermetallic compounds. For the PVD process application to terminal light alloy compositions is discussed."

Jan 1, 1994

By Yong Hack Lee

Electric Arc Furnace (EAF) dust is generated when scraps are treated in the electric arc furnace and usually classified as hazardous industrial waste in most countries. EAF dust usually contains 15 to 25% of zinc and 3% of lead. It is usually treated in rotary kiln (Waelz process) or landfilled after a solidification and stabilization treatment. Numerous methods have been proposed as the EAF dust treatment technology, but few of them are in operation as a commercial scale except the Waelz process. Korea Zinc performed a plant test in which 600 tons of EAF dust was treated using TSL (Top Submerged Lance) technology. The TSL technology is a low cost, proven technology for processing zinc-bearing residues. The EAF dust was first de-chlorinated and fed to the TSL furnace. Finally, clean slag satisfying toxicity criteria was generated and valuable metals such as zinc and lead were recovered as fume oxide. The fume oxide was de-halogenated by sodium carbonate and sent to zinc refinery to recover zinc and lead. The recovery of zinc and lead was 90% and 93%, respectively. Most of the dioxin in the EAF dust was discomposed so dioxin less than the Korean regulation limit was detected in the offgas, which proves that the TSL technology is the best solution to treat EAF dust.

Jan 1, 2006

By Marietta Canty

A paper is presented in which an innovative biological process is described for the treatment of cyanide-, metals-, and nitrate-contaminated mine process water. The technology was tested for its ability to detoxify cyanide and nitrate and immobilize metals in wastewater from agitation cyanide leaching. A pilot-scale demonstration is described in which a pilot plant was constructed to demonstrate the technology on a mine process waste stream at a mine in Nevada. The demonstration was performed Jointly under the Mine Waste Technology Program (MWTP), which is funded by the U.S. Environmental Protection Agency (EPA) and is jointly administered by the U.S. Department of Energy&apos;s (DOE) Western Environmental Technology Office (WETO) and the Superfund Innovative Technology Evaluation (SITE) Demonstration Program under Interagency Agreement Number DW89938513-0 I-0. MSE Technology Applications, Inc. (MSE) located in Butte. Montana, was the contractor responsible for conducting the project, and Pintail Systems, Inc., of Aurora. Colorado, was the technology provider. The pilot-scale unit was field-tested at the Echo Bay McCoy/Cove Mine southwest of Battle Mountain, Nevada. The biotreatment process was considered to be successful in destroying cyanide in the mine process water. The process was also determined to be effective in removing metals. The pH was consistently neutralized, and nitrates were successfully removed from the mine process water. As a result of conducting these pilot-scale tests, the biotreatment process was concluded to be an innovative, cost-effective alternative for the treatment of mining wastewaters.

Jan 1, 1998

By Norihiko Fukatsu

In order to use effectively the previously reported new sensing system for hydrogen and oxygen potentials in molten copper, the criteria of the potentials for getting sound castings have been determined in the laboratory experiment. The copper melt equilibrated with a given hydrogen and an oxygen potential was rapidly quenched in the crucible. The relations between the holding potentials and the gas porosity in the solidified sample were investigated by measuring the density of the sample and microscopic observations. It was found that the defects of the gas porosity became the maximum at the potentials where the dissolved amount of hydrogen and oxygen was in the mole ratio 2: I. The samples having the density more than 99% of the theoretical value were obtained in the higher oxygen and lower hydrogen potential region or in the lower oxygen and higher hydrogen potential region. The criteria thus determined were examined by comparing with the measured potentials in the practical easting machine. In tough-pitch copper casting, the problem due to gas porosity was found to be serious when the hydrogen potential increased. In the oxygen-free copper casting, the evolution of hydrogen was found not avoided. The gas porosity in the casting, however, was found eliminated when the oxygen potential was kept at a low value.

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 Rainer Schmid-Fetzer

"Isothermal solidification can be used to form strong bonds at low temperature which remain solid at much higher temperatures. The exploitation of this principally known technique for new high temperature processing steps and applications in electronic assemblies is the aim of this study. Three basically different variants of this bonding process are given. A comprehensive metallurgical screening is performed and the feasibility of binary material systems is given on a quantitative scale. Very attractive systems are spotted that have never been studied before. Detailed examples for the realization of bonding with complex ternary and multilayer systems are given. A highly innovative example is the chip stack or wafer to wafer bonding of unmetallized Si or SiC at 250°C. The proposed bond remains stable above the melting point of Si and enables entirely new semiconductor manufacturing steps. An improved die bonding process was proposed and verified experimentally.1. IntroductionIsothermal solidification can be applied to form strong bonds at relatively low temperature which remain solid at higher temperatures. The general principle of this type of joining processes is illustrated in Fig. 1. An interlayer of a low melting component, Lo, is provided as a foil or a thin film coating between the high melting joint components, Hi. The assembly is heated under moderate pressure to the bonding temperature, T 8 , and a liquid filler forms, either because the melting point of Lo is exceeded or due to a eutectic reaction between Lo and Hi. This molten filler initiates a rapid interdiffusion or reaction diffusion between Lo and Hi and the subsequent approach to an equilibrium state results in isothermal solidification. The solid phases formed at T 8 in the joint region exhibit a remelt temperature above T8 •"

Jan 1, 1996

By Alejandro R. Alonso, Lizet Alvarado, Gretchen T. Lapidus

"Cobalt and lithium recovery from spent Li-ion secondary batteries has been increasingly studied in recent years due to the high value of both metals and the low proven reserves for lithium. The standard method employed until now has been the deactivation and crushing of the batteries, followed by leaching of the L1C0O2 spinel from the battery cathode using acid solutions, such as 1.5 to 2.0 M HC1 or H2SO4, in a temperature range from 120°C to 250°C. Once leached, the cobalt is separated by electrodeposition and the lithium by precipitation, using large amounts of carbonate to bring the solution to alkaline pH values. In the present work, citric-thiosulfate solutions are used for the spinel leach at room temperature, favoring a reductive environment at room temperature, which stabilizes the cobalt(II) as cobalt citrate and lithium(I) at pH 5, and recovers approximately 99% of both metals.IntroductionThe Li-ion batteries industry has become an important economic sector in recent years. This type of battery is the most promising system for energy storage, because of its high efficiency in charge-discharge cycles, and its adaptability to many configurations. The demand will probably increase because of the need for mobile energy sources in many types of devices ranging from cell phones, tablets, and laptops to medical, navigation and sophisticated communication equipment and even in automobiles.One major problem related to the use of these batteries is the method employed for recycling the components, mostly cobalt and lithium. Currently, there are two processes employed on an industrial scale: the Sony/Sumimoto process, used since 1990 [1] and the Toxco Process [2]. In the first case, incineration is used to open the batteries and at same time volatilize the organic solvents. After that, the metals (copper, iron and aluminum) are physically separated. The cobalt and lithium are recovered as oxides and then thermally treated in order to recycle them for new batteries manufacture."

Jan 1, 2012

By Jin Liu

In the early 1990?s, Inco successfully installed two new flash furnaces as part of their SO2abatement project to reduce SO2 emissions from the Copper Cliff Smelter by 60%. The flash furnace off-gas is cooled and cleaned through two new Monsanto Dynawave gas cleaning systems that replaced the traditional venturi scrubbing system. It was discovered that the flash furnace production capacity is often limited by the capacity of the gas cleaning system. The key task is to eliminate pressure drop from the system. The froth column is responsible for by far the largest pressure drop in the gas cleaning system. Initially, the column was fitted with 22 plates. In 1994, both #1 and #2 froth columns were modified by reducing the number of plates in each column from 22 to 18 and increasing the interplate spacing on lower plates. With increasing demand for more throughput in the flash furnaces, further modifications on the froth columns were made in 2005. This paper describes these modifications and results together with some fundamental analysis of the froth column characteristics.

Jan 1, 2006

By Peter K. Everett

One of the major driving forces behind the development of the Intec Copper Process has been the increasingly stringent regulations governing SO2 emissions and, in some parts of the world, a declining H2SO4 market. Other incentives include operating cost (9.2 US c/lb Cu), capital cost (US $1400/annual tonne Cu compared with smelter cost of US$3-4000/annual tonne Cu) and the ability to treat low grade and contaminated concentrates. With such advantageous features, widespread use of the process is expected over time, leading to the production of large amounts of residues containing around 25% elemental sulfur, together with approximately 50-60 % akaganeite (FeOOH) and the ganggue minerals originally present in the concentrate feed. This paper briefly describes the Intec process chemistry involved in the formation of elemental sulfur, thereby avoiding atmospheric sulfur dioxide pollution, and the investigations to be carried out either to extract it or to turn the residue into a valuable by-product while minimising any adverse environmental effects, The process is being developed jointly by a group of fifteen major international mining companies.

Jan 1, 1996

By Keith Rozenburg, Ivar Reimanis, Jesus Chapa

"Experiments in conjunction with finite element analysis (FEA) are used to better predict crack propagation in ductile/brittle graded composites. Cu/W graded composites were fabricated by stacking discrete layers of powders and hot pressing. Crack propagation was studied by loading a notched beam in four point bending and examining the subsequent crack deflection. The notch was placed within a particular composition of material, oriented in a direction perpendicular to the gradient direction. Elastic and plastic mismatch between different constituents in the graded composite induce shifts in the phase angle of loading, thereby causing the crack to deflect. FEA indicates that thermal residual stress has a negligible ""influence on the crack path. The combined FEA and experimental results suggest that elastic mismatch is the single most important material property-related factor in controlling crack deflection.IntroductionMany 'applications would benefit or may even require materials whose performance or functionality must vary spatially. While the concept of functionally graded materials has existed for nearly one hundred years, it is only within the last fifteen years, that research efforts have focused on generic issues in processing, properties and performance of functionally graded materials. This generic research effort has brought together scientists and engineers from traditionally different disciplines to address common issues with graded composites. The current work focuses on issues in structural joining. A wide variety of applications require some type of joining between dissimilar materials. Examples include thermal barrier coatings for turbine engines, wear resistant coatings for tools, ceramic engine parts, and microeiectronic devices, as well as many traditional applications involving metallic welding. The joints may either be discrete, involving a single interface, or they may· be spatially graded in composition. Extensive theoretical and experimental information exists on discrete bimaterial and trimaterial joints, but relatively little exists for graded joints or composites"

Jan 1, 2000

By C. O. Bounds

The performance of AB5-type alloys for hydrogen absorption including the electrochemical absorption as an electrode for rechargeable batteries has been demonstrated&apos; to be a complex function of the composition, microstructure and surface condition. The compositional studies have focused primarily on substitutions for Ni on the B-site (e.g. Co, Al, Mn, etc.). This current study examines the effect of rare earth substitutions for La on the A-site and considers both other "light" rare earths (Ce, Nd, Pr) and "heavy" rare earths (Dy, Sm, etc.).

Jan 1, 1997

By Shu Xinqian, Zhou Weining, Shan Zhiqiang, Feng Jifu

"Modified calcination conditions on the extraction of rubidium resources from muscovite (KAlz[AlSi301o](OH)2) ore are systematically studied. The impact of various factors on the rubidium leaching rate is also analyzed, including the agent types, roasting time, the mass ratio, roasting temperature, etc. The results indicate that the best agent is a combination of sodium chloride and calcium chloride, its mass ratio ofmuscovite/NaCl/CaClz is 1:0.25:0.25. Calcined at 8500 for 30 minutes, the rubidium leaching rate is up to 90%. The reaction of muscovite ore with the chlorinating agent CaC12 has been studied by TG/DSC, the calcined intermediates are identified by XRD, and the surface morphology before and after leaching is characterized by SEM. Rubidium chloride products can be obtained with a purity of 92% by using t-BAMBP extraction, hydrochloric acid reextraction and purification.IntroductionRubidium is one ofrare alkali metals, which is found in 1981 by German R.W. Bunsen and G.R. Kirchhof. Rubidium includes the following features: atomic number is 37, each atom weight 85, the body-centred cubic lattice, each unit cell has two metal atoms, and the density is 1.532g/cm3. The properties of low melting point (312.46 K) and malleability make rubidium have a strong chemical activity and photoemission. Rubidium provides a main material for manufacturing phototube with a wide range oflight waves, which possess high sensitivity and stability. Efforts are being made to carry out research on rubidium ion gngine, magnetic flux generators and thermoelectric transudcer, etc. Rubidium exists in muscovite ore(KA12[AlSh01o](OH)2 (monoclinic system and hexagonal layered structure) as isomorphism and replace the large radius of the potassium atoms, as well as part of rubidium locate between structure layers. The complex components bring great difficulty in comprehensive recycling."

Jan 1, 2013

By P. C. Chaubal

The overall kinetics of oxidation of single partic1es of chalcopyrite have been studied for temperatures up to 1273 K. The experiments were conducted in a stationary bed reactor using a non-isothermal technique. Any mass and heat transfer effects on the kinetics of oxidation were eliminated by using a high-enough gas flowrate. Up to temperatures of 873 K, pore-bl1ocking kinetics were applicable, whereas above 873 K, power-law kinetics gave a satisfactory fit of the data. The activation energy was 215 kJ/mol below 754 Kand 23.7 kJ/mol above 1,060 K. Predominance area diagrams were constructed at various temperatures and used in conjunction with X-ray analyses of partially oxidized samples to determine the intermediate phases formed during the reaction. The analysi1s also provides a justification for the kinetic models used. The results indicate that the reaction rate is first order with respect to oxygen concentration and inversely proportional to the square of the particle size throughout the ranges of temperature studied.

Jan 1, 1985