Search Documents

By Masayasu Kawahara

"The extraction and separation of nickel, cobalt and copper were investigated with a solvent impregnated resin which was produced from UX84-I and XAD-4. The extraction behavior of metals with the solvent impregnated resin is similar to that with solvent extraction. The extraction ability of solvent impregnated resin improves when using finer particle resin and with a higher concentration of extraction solvent.IntroductionSolvent extraction is well known-as a method for separation of metallic elements in solution. However there are problems with intermediate phase and solvent loss. Ion exchange resin is also used in hydrometallurgy, but it is not fit for separating a large quantity of metals. Amberlite XAD-4 resin is known as a absorption agent of organic matter in water. It is expected that the resin which has the ability of extracting metals can be made by absorbing organic extractant on XAD-4 resin In this study, solvent impregnated resin (SIR) was produced from LIX84-I and XAD-4, and extraction and separation of nickel, cobalt and copper were conducted using SIR. The extraction properties of SIR were investigated, and a comparison between ordinary solvent extraction and SIR was made.Experimental ProcedureAmberlite XAD-4 was used as absorption resin for the organic extractant in this study. The physical properties of XAD-4 are shown in Table I. Amber lite XAD-4 has a large surface area and shows good ability to absorb organic matter in water, but the: resin does not have the ability of exchanging metallic ion."

Jan 1, 2000

By Donald L. Stewart, Ken Overfield, Edward M. Williams

"Recent increases in energy cost have lead to a renewed focus on energy efficiency during aluminum melting operations to reduce fuel usage. The goals of a batch melting operation are to melt the charge using the minimum required energy, to melt the metal to the required temperature within the required timeframe, and to avoid generating unwanted contaminants by overheating the charge.The heat transfer efficiency of a conventional hydrocarbon fired aluminum melting furnace varies over the course of the melt cycle, depending on the conditions in the furnace. The purpose of this work was to develop a method of determining the transient heat transfer efficiency throughout the furnace cycle and to take advantage of this knowledge to optimize the melting process through furnace controls and proper production operations. This furnace survey methodology has been developed and used to evaluate a number of furnaces.Description of a Typical Batch Melting Furnace CycleA typical batch melting furnace cycle will consist of three stages:1. Charging – Solid metal charged through an open roof, solid or molten charged through an open door, and/or molten poured through a furnace blister2. Melting – From the time the door or roof is closed and the burners are turned to high fire until the charge is all liquid and has reached a temperature suitable for alloying (typically ~1350 °F / 730 °C)3. Holding – From the end of the melting stage until transfer or casting is completeIn some cases, further charging can take place after the melting cycle has started. This can happen when the entire solid charge will not fit in the furnace in one load, or if additional molten metal is added while the charge is melting. The bulk of the energy used in the melter is consumed during the melting cycle. The thermodynamic minimum energy requirements for melting pure aluminum are:• Energy required to heat pure aluminum from room temperature to the melting point at 1220°F (660°C) is 288 BTU/lb (670 kJ/kg)• Energy required to change state of pure aluminum from solid to liquid (heat of fusion) is 171 BTU/lb (397 kJ/kg)• Energy required to heat molten from melting point at 1220°F (660°C) to 1350°F (730°C) is 36 BTU/lb (83 kJ/kg)• Total energy required to melt a solid charge from room temperature to 1350°F (730°C ) is 495 BTU/lb (1151 kJ/kg)"

Jan 1, 2009

By Leonel Contreras

The gas treatment system, MALIGAS (in Spanish MAnejo y Llmpieza de GASes which means handling and cleaning of gas), is part of the Codelco-Chile Potrerillos Smelter decontamination plan; which includes the newly designed system for the cooling and cleaning of the gas generated from a Teniente Converter and four Peirce Smith Converters. The gas generated in the process is captured by water cooled hoods and mixed with air. Then the gas enters a cooling pre-chamber which utilizes a water cooled screen to capture and remove the coarse and semi-fused particles. At this stage; the gas loses a portion of its heat with temperature falling below 608°C which is a necessary condition to avoid damage to the pipes, ducts and other metallic structure of the gas handling system. The gas is further cooled at the Radiation Cooler to a temperature ranging between 315 and 380°C. The gas is conditioned to avoid damage to the electrostatic precipitators that are designed to clean the gas by removing significant amount of dusts from the: gas stream. This gas stream is currently discharged to the stack, however, it will be treated in a sulfuric acid plant that is currently under construction and is scheduled for commissioning during the second half of 1999. The gas handing and cleaning system has been operated without any significant interruptions. Minimal emissions of SO2 and dusts in the work place are noted. The system requires minimum maintenance. The key to the high availability of the system is due to the good, performance of he Radiation Cooler, which efficiently cools the gas before entering the electrostatic precipitators (ESPs). This enables the ESPs to remove the dusts efficiently.

Jan 1, 1999

By Min Chen, Cui-huan Huang, Zhen Tian, Jian-hong Dong

"The present work studied the production of Fe-Si-Mn alloy from adjusted converter slag by thermodynamic analysis. The results showed that solubility of SiO2 in the molten slag increased with increment of temperature, and it is about 80% at 1800 ?. With increment of SiO2 content, a(MnO) and a(CaO) decreased, and a(FeO) increased to the maximum when w(SiO2) is about 30%. As a result, the reduction of the slag was in the order of Fe?Mn?P before SiO2 reduction, the reduction order was Fe?P?Mn?Si when SiO2 content in the slag was from 46.4% to 54.2%, and changed to Fe?Si?P?Mn when SiO2 content exceeded 54.2%. The mass fraction of Si in the alloy phase increases with increasing of w(SiO2) in the slag, and the mass fraction of Si in the alloy reached to 62.2% at 1800 ?.IntroductionFerroalloy production is a high energy consumption and high pollution industry[1-2]. If ferroalloy production could be produced from molten slag by addition of carbon-reducing agent, the valuable metal and oxide in the slag can be recycled, most importantly, if the high-temperature resource carried by molten slag can be made full use in the field of ferroalloy production, the power consumption of ferroalloy production could be cut down greatly.Converter steel slag is a kind of byproduct in steelmaking processing increasing rapidly with the increment of crude steel, but the utilization ratio is low. Most heat recovery research is still in the experimental stage except the heat recovery of blast furnace slag by water quenching method, at present[3-4]. It is of great significance for enterprises to energy saving and emission reduction if the molten steel slag could be utilized directly. Not only the reuse methods of liquid steel slag material can be promoted, but also the use of heat carried in the slag could be achieved. The basicity of converter slag is high and the activity of SiO2 is low so the reduction of SiO2 in the slag is little. The compositions of slag and metal phases were calculated by Factsage program on different conditions to explore the reduction of converter slag for recovery of valuable metals and an efficient new way to use the high-temperature heat combining with the current reuse and research status of converter slag. Further, the improvement of components activity in slag and the increase of Si concentration in the metal were also dicussed."

Jan 1, 2012

By E. L. Frueh

AMAX Base Metals Research & Development, Inc. has developed a process for treating copper-nickel mattes to produce copper cathodes and a pure nickel sulfate solution. In this process, the input matte is preleached in a copper sulfate electrolyte bleed solution so as to dissolve nickel from the matte and cement copper from solution. The preleach leaves a substantially pure nickel sulfate solution. The residue from the preleach is roasted to less than about one percent sulfur. A portion of the calcine is leached with sulfuric acid to make a copper sulfate solution for input to the tank house. The residue from this leach and the remaining calcine are smelted to form a bimetallic (copper/nickel.) anode. The anodes are electrolytically refined and copper is preferentially deposited on the cathode while the nickel reports to the electrolyte, A bleed stream is taken from the electrolyte and used in the preleaching of the input matte. This process produces high purity metal streams while consuming less energy and smaller amounts of reagents as compared with other matte processes.

Jan 1, 1983

By Tobias Dubberstein, Hans-Peter Heller

The viscosity of Fe-Cr-Mn-Ni TRIP/TWIP (Transformation Induced Plasticity, Twinning Induced Plasticity) steel with varied nickel content is investigated using a vibrating finger viscometer. The viscosity of the melt is calculated from the change in power input in the field coil by an immersed finger into the liquid steel to maintain a constant peak-to-peak amplitude of the sine wave of oscillator compared to the idle state. Nickel content in steel is varied from 3 wt% to 9 wt%. The dynamic viscosity (η) at 1600 °C for 3 wt% Ni is 3.73±0.14 mPas, for 6 wt% Ni 3.50±0.03 mPas, and for 9 wt% Ni 3.93±0.09 mPas. There is a kink from low to high nickel content in viscosity values of Fe-Cr-Mn-Ni alloys. This phenomenon can be explained by a change in coordination number in the melt, as reported for Fe-Ni binary system in literature. The availability of viscosity data delivers relevant input to model free fall atomization processes of FeCrMnNi alloys.

Jan 1, 2015

By Shigem Kuramoto

Pure copper is known to exhibit intermediate temperature embrittlement when it is deformed at a slow strain rate, and a small addition of zinc suppresses this embrittlement. In the present study, the relation between zinc addition and hydrogen behavior was taken into account since the impurity hydrogen is believed to deteriorate the ductility at intermediate temperatures. Pure copper and Cu-l mass % Zn alloy specimens are prepared by melting in argon and in vacuum, so that a comparison can be made between the specimens with normal hydrogen content and those with' less hydrogen content. Tensile tests are performed at temperatures ranging from room temperature to 600 "C, and hydrogen behavior is analyzed using a newly developed testing machine that can detect gas evolution from the specimens during deformation and fracture in ultra high vacuum. The small addition of zinc to pure copper decreases hydrogen content, leading to the improved ductility at intermediate temperatures. In addition, the samples of both pure copper and Cu-1%Zn melted in vacuum exhibited higher ductility at intermediate temperatures than those melted in argon atmosphere, which is attributed to reduced hydrogen content.

Jan 1, 1998

By Chikabumi Yamauchi, Masami Tashiro, Toshiharu Fujisawa, Hiroyuki Snano

"Rare earth metals usually contain large amount of oxygen because of their reactiveness, and therefore oxygen removal is one of the major problems on the purification of rare earth metals. In the present research work, halide flux treatment at high temperature under inert gas atmosphere was applied to the oxygen removal from neodymium. NdF3 was used as a halide flux. Deoxidation reaction and its mechanism were discussed based on the experimental results. Halide flux treatment is very effective for oxygen removal from rare earth metals.IntroductionSolid Sate Electrotransport (SSE) process has been successfully applied for the elimination of interstitial gaseous impurities from chemically active metals[l]-[5]. However, to achieve a higher effectiveness of the SSE process, it is required a very low initial impurity content in the metal. In case of rare earth metals, it is known that they usually contain large amount of oxygen that should be lowered as much as possible before applying the SSE process. In addition, if effective oxygen removal is achieved by simple process, it is significant also from the industrial viewpoint. In the present work, the application of a halide flux treatment is investigated to remove oxygen from neodymium by using NdF3 as a flux. At first, deoxidation reaction and its mechanism were discussed based on the phase diagram of the Nd-NdF3-Ndp3 quasi-ternary system. Based on the results, oxygen content in deoxidized neodymium was calculated theoretically and it was verified by deoxidation experiments."

Jan 1, 1998

By Leijun Li, M. M. Mahapatra

"A three-dimensional finite element model with moving heat source was developed for pulsed-laser powder deposition (PLPD) process. Experiments were conducted to study the repair of superalloy components using the PLPD process. During the experiments, IN 625 powder was deposited on a superalloy substrate similar to IN 738. The process was modeled using three-dimensional finite element analysis. Element birth and death technique was used in the finite element model for simulating the deposition of powder layer on the substrate. A moving distributed heat source was used in the thermal model for realistic simulation of the process. Temperature dependent thermal material properties including enthalpy were used for the powder and the substrate in the transient thermal analyses. The fusion zones and peak temperature distributions of the deposits were predicted from the transient thermal analyses.IntroductionPoor weldability is a critical issue of superalloy repairing. The microstructural directionality of the superalloy components are disrupted when repaired by the fusion welding processes. Currently there is no widely accepted method to economically and reliably repair directionally solidified superalloys components. Pulsed laser powder deposition process (PLPD) is a promising repairing technique as the substrate is not severely affected by the heat source.In this study PLPD technology is used as the tool for superalloy repairing. In most of the land based turbine engines the directionally solidified nickel based superalloy similar to IN 738 [1] is used as the bucket material. The turbine engine blade tips are subjected to a combination of extreme operating conditions and corrosive environment. The tip of the nickel based turbine engine blades can be repaired using IN 625 material as suggested in the literature [1-2]. IN 625 is considered to be ductile and strong enough for the purpose of Ni based turbine engine blade tip repair[1-2]. During the present PLPD investigation, IN 625 powder was used as the deposit material on an experimental super alloy substrate similar to IN 738 superalloy used as the cast superalloy for the turbine engine blades."

Jan 1, 2012

By Marcelo R. Esquivel

A MmNi5 alloy is synthesized by a combination of mechanical milling and low temperature heating processes. Synthesis time is 40 h for powders milled in a low energy ball mill at room temperature. A reduction in milling time is obtained if massive sample is mechanically milled at shorter times (2 h to 10 h) and heated at temperatures lower (600 ºC) than the usual temperatures used in equilibrium methods (>800 ºC). The alloy formation is detected even at a combination of temperatures as low as 200 ºC and milling times as short as 5 h. The temporal evolution of mechanical milling process was followed by both X-ray diffraction (XRD) and scanning electron microscopy (SEM) to detect the main stages of milling. Four stages were detected: Initial, Intermediate, Final and Completion. These stages were correlated to an enhancement of the synthesis method by combination of times of milling shorter than 10 h and temperatures of heating lower than 600 ºC.

Jan 1, 2006

Sodium is added to aluminum-silicon eutectic alloys to modify the structure. The ideal amount is about 100 ppm but due to the fact that sodium is lighter than aluminum and can float to the surface where it bums, oxidizes ad volatilizes, a far greater amount is usually added. Furthermore, as the sodium is continually lost from the alloy the optimum amount is only present for a limited time. The net result is a process which is hard to control, produces fumes and a considerable amount of dross. It is shown that by electrochemically titrating sodium through a tube of sodium beta alumina electrolyte that the sodium can be added continuously in a controlled way. As the sodium is added to the bulk of the aluminum, there is no sodium on the surface of the alloy so that little surface oxidation occurs, and no fumes and dross are produced. This leads to an improved product and working conditions.

Jan 1, 1995

By Mitchell L. Spencer, Viswanathan Panchanathan

"Bonded magnets are important category in permanent magnets. They are made by one of the following processes: compression bonding, injection molding, extrusion, calendering. An overview of the various bonded magnet processes and properties of products made with different magnet materials along with their applications are discussed. The main emphasis will be on the use of bonded NdFeB and ferrite magnets.IntroductionBonded magnets are a major growth area in permanent magnets. Bonded magnets are made by any one of the following processes: Compression bonding; Injection Molding; Extrusion and Calendering [1,2]. Compression and injection molded magnets are rigid magnets. Materials used in calendering process produce flexible magnets. Only the extrusion process makes both rigid and flexible magnets. The binders used for the bonded magnets vary depending on the processes. Thermoset, thermo-plastic and elastomeric binders are respectively used in compression, injection and the calendering process. Extrusion molding uses elastomers or thermo-plastic materials. The most co=on magnetic materials, Ferrite, SmCo, Alnico and NdFeB can be used in any of the above processes either alone or in combination as hybrid magnets. Another material that has been developed for co=ercial application is SmFeN. Making the material has been challenging and it is being used in niche market applications in limited quantitiesIn the extrusion process, a highly loaded compound is used to produce strip or sheet and is continuously extruded through a die. In calendering the granulated compound is rolled to produce a continuous wide sheet. In the compression bonding process a uniaxial pressing force is used. These magnets have higher loading compared to injection molded magnets. In injection molding the material is forced into a mold cavity and has lower loading compared to compression molded magnets [2,3]. Most of the flexible magnets are made using extrusion and calendering processes and the most co=on magnet material is inexpensive ferrite. Flexible magnets have been made using rare earth materials, but on a very limited basis.The major advantages of magnets processed by extrusion and calendering are as follows: inexpensive tooling, automation; practically any 2D geometry; fast production rates; no chipping or breaking; a wide range of properties; on-line magnetization; easy to convert (e.g. cut, punch or shape).Compression bonded magnets are inexpensive to manufacture. They have higher magnetic properties compared to injection molded magnets; however lower than their sintered counterparts. The magnet shape is restricted to simple geometries and they require careful handling. Their isotropic nature allows complex magnetizing patterns."

Jan 1, 2013

By Keiji Okumura, Hong Lan, Masamichi Sano

"Magnesium has been well known as one of the excellent agent of desulfurization, deoxidation, etc. in iron- and steelmaking because of its high reactivity. Since its production is energy nitensive, the price is very high. Thus magnesium has not widely been used as an agent in metal refining ·processes. In the present work, reduction of magnesia by carbon and aluminum is examined. Because the reaction is very sensitive to temperature, non-isothermal technique is applied to investigate the reaction kinetics. The effects of heating rate .and reaction interface area on the reaction kinetics .are studied. .A kinetic model is proposed based on the experimental results.IntroductionFor the metal refining processes, the production of high purity metal has been one of the most important research subject. In order to produce the high purity metal, the amount of the refining agent and the consumed energy is increasing. Therefore, if the future earth environment is taken into consideration, the further efficient and energy saving processes are required. Generally, Cao slag has mainly been used for desulfurization of molten iron as a desulfurization agent. However, environmental problems, such as recycling of disposal slags, are still unsolved. On the other hand, the deoxidation of molten steel is mainly performed by addition of aluminum. Therefore, the alumina inclusions· remain in. molten steel and the great efforts have been made to the removal of the inclusions. The affinity of magnesium with sulfur and oxygen is strong, and magnesium is well known as a powerful desulfurization and deoxidation agent. However, magnesium has been seldom used for the steel' refining process. The following reasons are considered. Generally, magnesium is expensive. And at iron- and steelmaking temperatures, the refining efficiency becomes low due to its abruptly .evaporation."

Jan 1, 2000

By Tomoya Nihei, Hiroshi Hayashi

"A novel selenium removal process called Recycled Green rust/Ferrite Process is developed by MMC. In this process, a mixed Fe2+-Fe3+ hydroxide compound, green rust (GR), reduces selenate to elemental selenium, while GR is consequently oxidized to magnetite Fe3O4. Sequencing batch-mode experiment showed that the residual selenium concentration gradually decreased with the number of batch test increased. Stable selenium removal was achieved when the number of batch test exceed 15 times. Optimum selenium removal ratio reached 99.95% where initial Se concentration 2.1mg/L decreased to 0.001mg/L. Furthermore, the continuous feeding test carried out through a pilot-scale plant with a feeding capacity 600 L/hr. Approximately 860-hour-feeding test was carried out for the selenium-contaminated groundwater which had an averaged selenium concentration of 0.88 mg/L. Selenium concentration in the effluent from thickener maintained less than 0.01 mg/L (selenium removal rate of 99%) until a net operating time reached 800 hours.IntroductionJapan is one of the largest producers of selenium, and thus there are potential environmental impacts of selenium on soil and aquatic environments. The Mitsubishi Material Corporation (MMC) owns some real estate properties whose soil and groundwater was polluted by selenium and other heavy metals. These sites include former industrial plants: a smelter for nonferrous metal and a fabricating semiconductors and pigments. Selenium in aquatic environment commonly exists in four oxidation states, namely, VI, IV, 0 and -II. Selenate ion (SeO4 2-), the most oxidized form of selenium, and selenite ion (SeO3 2-) are highly soluble and mobile. Elemental selenium (Se0) is insoluble in water and therefore has much lower toxicity. Because selenium is carcinogenic and teratogenic at high concentration, the national effluent standard in Japan is fixed at 0.1 mg/L and the environmental standard at 0.01 mg/L. Although there are several selenium removal techniques, the most conventional process is coprecipitation with a ferric hydroxide because of its simplicity and low cost. It is known that selenite is adsorbed strongly on the surface of ferric hydroxide, but selenate is not. The low affinity of selenate on oxide mineral surfaces was demonstrated by the fact that selenate could be easily displaced by adding competing anions, particularly sulfate ion. Selenate removal from polluted water is one of the most difficult techniques, and more effective methods are desired. MMC developed a novel selenium removal process [1]. In this process, the concentrated slurry that contains Fe(II)-Fe(III) hydroxyl-salts known as Green Rusts (GRs) contributes to selenate removal. The main components of the iron precipitate in the reactor are GRs and their oxidation product, magnetite (Fe3O4)."

Jan 1, 2008

By C. Niedersberg, M. K. Almeida, R. M. C. Santana, V. G. Dalenogore

"The major source of environmental pollution in urban areas is the transport sector and its impact on human health and the greenhouse is preoccupying. In many works of literature is monitored the pollutants in urban cities, however in specific areas such as universities, they are scarce. Therefore, the aim of this work is to monitorate the gaseous pollutans in a bus terminal at Santa Cruz do Sul University-UNISC and to develop a control framework of the air quality. Six points were selected for monitoring, being one of them inside a bus. The monitoring of CO, HC and CO2 were carried out on arrival and departure of the bus. Preliminary results conducted in a day of spring showed that the most critical condition was during the night shift, where the concentration of CO (200 ppm) was the highest, caused by the vehicles increase, due to the larger number of students.IntroductionAccording to Mascarenhas et al, 2005, air pollutants are responsible for various effects on vegetation, ecosystems and is recognized as one of major public health problems of today, with harmful effect on humans even at levels considered safe by Brazilian legislation.There are numerous scientific papers linking air pollution with respiratory problems, cardiovascular which hinder the daily life because many of these diseases are chronic and may even lead to death, as was noted by Brook et al, 2004.There is a significant increase in the last decades of emissions to air resulting mainly from human activities. Already being observed the relationship of these emissions with the change in global climate, IPCC, 1995.They are a multitude of pollutants from the atmosphere, and its sources and its effects. The effect of Greenhouse gases (GHG), representing less than 1% of the gases in the atmosphere, controlling the flow of energy in the atmosphere. The increase in emissions of greenhouse gases is affecting the Earth's average temperature, which depends on the balance between these flows, in particular the flow of solar radiation reaching the surface and the flow of infrared radiation sent into space.One of the main greenhouse gases to this imbalance is the gas methane (CH4). Methane is produced by anaerobic decomposition of organic substances, through the action of bacteria metanogenic conditions that require highly reduced to its growth. This gas is released into the atmosphere mainly by transport diffusive by aerenchyma (vascular tissue) plant and also by diffusion through the water slide. (Bont et al., 1978)."

Jan 1, 2008

By Samantha Moodley, Rauf Hurman Eric, Cevat Kucukkaragoz, Aditya Kale

"Two titania slags, rutile and synthetic rutile were chlorinated with petroleum coke and CO in a small bubbling fluidized bed reactor. The study aims to identify differences in chlorination mechanism, compare conversion rates, blowover and the chlorination of impurities for the various titania feedstocks at different temperatures.Chlorination rates were highest at 1000ºC; rutile chlorination significantly increases as temperature increases from 800ºC to 1000ºC. At 1000ºC, synthetic rutile had the highest chlorination conversion rate; this was followed by Slag B which in turn was more reactive than Slag A and rutile. The mechanism for slag, synthetic rutile (SR) and rutile chlorination differs. Synthetic rutile feed is porous, providing a larger surface area for the chlorination reaction, hence the highest conversion rates was attained. Titania slag becomes porous with the initial chlorination of FeO and MnO whilst rutile remains solid. As the porosity of slag particles increases so does its tendency to be elutriated. Ti2O3 is oxidized within the early stages of chlorination during the chlorination of FeO and MnO. Ti2O3 not oxidized is then rapidly chlorinated.IntroductionTitanium dioxide (TiO2) is the most common compound of titanium, about 95 - 98% of extracted titanium minerals is processed into TiO2 white pigment [1]. Two processing routes exist for the production of TiO2 pigments, i.e., sulphate and chloride based processes. In the chloride process, titania feedstock is fed to a fluidized bed reactor together with reductant and chlorine gas. A temperature of 1000 - 1300ºC is maintained in the reaction zone and apart from silica, zirconia, uranium and thorium, virtually all the metal oxides in the feed are converted to their respective chlorides [2]. Chlorine is recovered and recycled back to the reactor."

Jan 1, 2012

By Raj Mutharasan

The phenomena of gas-molten metal reactions for the production of metal matrix composites consist typically of a combination of one or more gas transport steps and a liquid gas reaction step. Reaction products include such strength enhancers, grain refiners, or high thermal conductivity phases as TiC, AIN, SIC, Si3N4, TiN in aluminum alloys. Nitrides, carbides and oxides can be produced at various volume fractions and in fairly fine sizes (500 am to 5 um) in laboratory melts by Reactive Gas Injection method (RGI). Gas injection methodology to produce the reinforcements is attractive because it can potentially be scaled to production scales in excess of 10,000 kg/h. For continuous production, the reactant molten metal can be continuously fed into the .crucible where the reactive gas is injected. The molten metal phase reactant may also be involved in a controlling transport step, depending on its concentration and viscosity. It is well known that the reaction product reinforcement size and shape of these phases have significant impact on the physical, mechanical and thermal properties. The current state of knowledge is unable to predict the kinetics and growth of solid reaction products obtained. The primary goal is to develop a fundamental framework for the understanding and prediction of the particle size in such reaction systems. In addition, the role of gas transport, liquid hydrodynamics and decomposition are important issues. A reaction-transport model is being developed using a reaction, transport, and thermodynamic framework, both at macro and at atomistic level to assess gas - liquid interactions.

Jan 1, 1996

By Robert Hanson, Mayur K. Patel

"Pneumatic conveying pipelines are used throughout a variety of industries, from food processing/packing to power generation plants, as an efficient means of transporting materials between storage and processing points. In general, different phases of pneumatic conveying exist when material is conveyed from point A to point B in a pipeline. This depends on the operating pressure and the material conveyed. Lean phase conveying exists when pipelines are operated at high airflow rates, relatively low pressures, inducing sufficient turbulence for particles to become entrained in the air stream. Thus, particles are conveyed along the pipelines at velocities in the range of IS-2Sm/s. Generally, the initial capital costs for lean phase system is low, however the running costs are high. The opposite is true for dense phase, high-pressure systems. In considering either conveying system, it is important that the rate of erosion of the pipeline be considered when designing such a system, since it is the rate of erosion that dictates the lifetime of components. In general, the high level of erosion occurs for lean phase flows, where high impact velocity contribute substantially to the rate of erosion as well as other processes such as particle breaking, if the particles are friable. This would lead to poor quality of material, not normally desirable. On a positive note, the process of erosion is used in other applications, which benefits from this process, e.g. abrasive guns.The failure, by puncture, of pneumatic conveyor bends in industry causes several major problems. Two of these are: (a) escape of the conveyed product causing health and dust hazard and (b) repairing and cleaning up after punctures necessitates shutting down conveyors, which will affect the operation ofthe plant, thus reducing profitability.The paper reports on modelling strategy used in the development of a modelling framework and the initial validation phases of the models incorporated within. The modelling framework encompasses Computational Fluid Dynamics (CFD) related engineering tools, based on Eulerian (gas) and Lagrangian (particle) approaches, to represent the two distinct conveyed phases, to represent the erosion process which is used to ascertain the lifetime of conveyor bends."

Jan 1, 2001

By Georgios N. Anastassakis, Nickolaos Georgiou

"Soil contamination by oil as well as by other organic pollutants poses a major problem to the environment. Various methods have been used to remove organic contaminants from soil, such as: biological, thermal, chemical and physical. Methods based on Mineral Processing principles have also been used (cyclone separation, gravimetric separation, attritioning and washing). This paper studies the possibility to remove a rich-in-contaminant soil fraction by applying flotation. The contaminated soil was artificially prepared by mixing soil with diesel fuel. Sodium dodecylsulfate (SDS) and a tertiary amine (TA) were used as collectors. The effect of collector quantity added and conditioning time was studied. The results showed that the removal of a rich-in-contaminant soil is feasible while a clean fraction is also obtained. In several cases, the removal of oil-contaminated soil approaches or reaches 100%. Introduction Human activities are intimately associated with environmental pollution to the air, water and soil, as well. Soil pollution from inorganic and organic compounds is of equal importance with that of air and water, as it results in soil degradation and its concomitant problems with respect to meeting the human needs (house building, agriculture etc). Heavy metals along with their compounds are encountered among the most usual soil inorganic pollutants. The corresponding organic soil-pollutants are oil, oil-derivatives, pesticides, various aromatic (benzene, phenols, cresols, toluene etc) and poly-aromatic (naphthalene, anthracene etc) hydrocarbons, as well as various other organic compounds (pyridine, cyclo-hexane etc). Oil remains the basic energy source sharing 38% of the global needs, being followed by coal and gas with a share of 26 and 21% correspondingly [1]. The entire activities related with oil production, transport and consumption promote pollution in the air, water and soil. Consequently, soil pollution from oil is favoured at refineries, storage sites (due to possible pipe and tank leakage, tank cleaning works, loading and transportation) and, finally, at the oil-selling sites. Oil (or diesel-oil) fuel is a mixture of hydrocarbons, with 10-20 carbon atoms in the chain of each. It is mainly composed of paraffins, naphthenes and various aromatic compounds. In general, oil is composed of 20-30% in aromatic compounds, 5-6% in naphthenes and the rest is paraffins [1]."

Jan 1, 2008

By R. Nilsson

In the present work, an assessment of the sulphide capacities of a number of binary and ternary slag systems have been carried out in the light of a sulphide capacity model. The model is based on the expression: {CS- exp (-A G °/R T) ? ao2 / fs2-} where AGO is the standard Gibbs energy change for the above reaction, ao2 is the activity of oxygen ions and f, is the activity coefficient of the sulphide ion in the slag. In the present model, the ratio (ao2/fs2) is optimized for the experimental data available in literature. The systems assessed are the binaries MnO-SiO2, CaO-SiO2, Al2O3-CaO, as well as the ternaries CaO-Al2O3-SiO2 and CaO-MnO-SiO2. In the case of all these systems, the experimental data available in literature were complemented by measurements carried out at the Division of Theoretical Metallurgy. The sulphide capacities of some FeO- containing binary, ternary and quaternary slags are also examined. The potentiality of the model to estimate the sulphide capacities of complex slag systems from binary and ternary data is demonstrated.

Jan 1, 1996