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By Ko-ichiro Ohno

It is recently recognized that the iron reduction and melting as well as the slag separation of a composite of granular iron ore and coal are completed in a very short period of about 10 minutes when the composite is rapidly heated up to approximately 1673K. These phenomena are expected to be applied to a new iron-making process. The mechanism of iron ore reduction and iron-slag separation during rapid heating has not yet been revealed and the fundamental research has just started. Carburization of the reduced iron is regarded as one of the most important steps in this process. In the present work, the composite was prepared from four kinds of coal or graphite as a carbon source and electrolytic iron powder as a completely reduced iron ore. The temperature at which the liquid formation and iron carburization occurred was monitored. Direct observation of smelting reduction behavior was made by a confocal laser-scanning microscope combined with the infrared image-heating furnace to clarify the effect of molten ash on iron carburization. It was found that the meltdown temperature of composite became lower as the melting temperature of coal ash decreased. From the observed result, it was presumed that the liquid slag would act as an important media for the carbon transfer from coal to iron. The carburization mechanism during the smelting reduction was estimated as follows. When slag containing iron oxide melted down and contacted carbon, iron oxide in the slag was reduced and the formation of the metallic iron particle as well as the its carburization occurred simultaneously at the slag-carbon interface. Carburized iron particle was carried from slag-carbon to slag-iron interfaces due to the slag convection flow caused by the difference of the interfacial tension between the carbon-slag and iron-slag interfaces. Carburization of reduced iron could proceed with a repeat of the above-mentioned process.

Jan 1, 2003

By Patrick R. Taylor

Keywords: Thermal Plasma, Electroreduction, Electrolysis, Transition metals, Waste treatment, Molten oxides, Chromium oxide. An innovative process to treat transition metal oxide waste materials from diverse sources is presented. This technology involves using reverse-polarity DC plasma driven electrolysis in molten oxides. The process results in the recovery of the transition metal and other heavy metals from waste. By-products generated throughout the processing was converted to environmentally acceptable slag. The significance of this technology is that the treatment of the waste is accomplished in one step which in turn lowers the cost of remediation. Moreover, this process uses high temperature properties of thermal plasmas, which makes it possible to use molten oxides instead of halides as electrolytes. Chromium was successfully reduced from chromium oxide through the plasma driven electro-reduction process. It was shown that the selection of the appropriate ionic conducting oxides was critical for the formation of a slag that would enhance the reduction of chromium oxide.

Jan 1, 2004

By Bruce H. Baker

Studies of used or unused refractory materials are excellent examples of applied mineralogy in industry. Refractory materials are mineral substances containing ceramic or chemical bonding systems. Knowledge of the mineral composition, bonding, and textural relationships often explains the resulting physical property values of a refractory and contributes to the interpretation of refractory wear mechanisms occurring in steel plant service.

Jan 1, 1982

By M. D. Crites

As part of a multi-year program for assessing the viability of chrome-free refractories in copper smelting, converting and refining furnaces, dynamic corrosion tests have been conducted on a series of refractories from the magnesia-alumina system, using a ferrous silicate slag. The corrosion rates of the test refractories are compared with those of a reference mag-chrome brick, and recommendations are made for more in-depth evaluations of the more corrosion-resistant materials.

Jan 1, 1999

By Lin Li, Xiang Li, Yifang Zheng, Jilai Xue, Jun Zhu

"Al drops and gas bubbles in the anode-cathode space of aluminum electrolysis cell are of great importance for cell operation improvement in metal loss, current efficiency and energy consumption. A direct observation on the Al drop, gas bubble and ultrasound was carried out through a see-through cell. The Al drop immersed into the cryolitic melt was found moving up and down irregularly in the anode-cathode space without electrolysis, which was then completely dissolved into the melt. During electrolysis, the Al drop came to the anode area and reacted with the gas bubbles generated on the anode. Under ultrasound, the gas bubbles were removed from the anode surface while the Al drop was kept on the side of anode. The observed phenomena were useful for technology improvement in reducing the anode-cathode distance or lowering the energy consumption in aluminum electrolysis.IntroductionDuring aluminum electrolysis, aluminum metal drop and anodic gas bubble are in close contact each other within the anode-cathode space, and the interaction between them can produce significant impact on metal loss, current efficiency and energy consumption. The motions of the Al drop and the gas bubble are also related to the dissolution of aluminum metal into cryolitic melt and the cell voltage drop due to the bubble layer covering the anode surface.A number of studies have been carried out using different types of see-through cells, where the dissolving process of metal Al into cryolitic melts (metal fog) in the anode-cathode space was directly observed and photographed [1, 2]. With the similar method, some direct observations on the anodic bubble behaviors with and without ultrasound were performed during aluminum electrolysis [3-6]. However, to our best knowledge, there is no published work on direct observation on the behavior of Al drops and anodic gas bubbles staying together within the same anode-cathode space, as well as the motion and interaction of them in cryolite-alumina melts."

Jan 1, 2011

By Valeriano Antonio Corbellini, Marilda Macagnan, Rosana de Cassia de Souza Schneider, Tiago Bjerk, Mariela de Souza Vieira

The great potential of Brazil for the agricultural production makes our country a generator of agro industrial residues. In this context, the solid-state fermentation appears as a technology that shows alternative ways for those residues, adding values to these raw materials, through the production of substances of industrial interest, besides reducing the possible environmental problems. The main objective of this study was to apply the bovine fat residue associated to the garden grass for the fungal lipase production. Initially, 75 microbial cultures were isolated from garden grass samples after incubation of the mixture with bovine fat. From these cultures were selected the filamentous fungi, whose lipase production abilities were evaluated. The isolation and the selection were accomplished by using a differential culture medium containing Tween 80 as inducer substrate of lipase production. The colonies with lipolytic potential were detected by the presence of white precipitation haloes on the agar. With agro industrial residues the best lipase producer fungus was identified as Penicillium sp in 6 days of solid state fermentation. The crude enzyme obtained was tested in transesterification process for the biodiesel production.

Jan 1, 2008

By Orlando C. Rojas

The Potrerillos Smelter commissioned a new El Teniente converter in 1985. As a result of the use of this technology, the Peirce-Smith converters have been processing only high grade matte or white metal. These operational changes resulted in damages to the converter shells, excessive splashing and cold dope generation and very short refractory campaigns. The paper shows the modifications to the tuyere angle, mouth design changes and new techniques for mouth cleaning and gas handling. Operational results up to 1991 are also shown.

Jan 1, 1993

By Yousef Mohassab, Manoranjan Misra, Monalisa Panda, Eman Wahbah

This work studies the removal of arsenic (V), arsenate, and arsenic (III), arsenite, from aqueous solution using calcined Quintinite-3T. The two adsorbents Quintinite-3T was prepared, calcined at different temperatures, and characterized by XRD, BET, and SEM. The surface area of the calcined Quintinite-3T was 193.4 m2/g. The particles size ranged from 12 to 56 nm for the uncalcined Quintinite-3T and from 24 to 42 nm for the calcined Quintinite-3T. Kinetic analysis, adsorption isotherm, and factors affecting the adsorption were investigated. Calcined Quintinite- 3T retained As(v) and did not release it back to water even after an entire month.

Jan 1, 2016

By Adele Garkida

Compacts of crushed waste window glass, fluorescent tubes, drinking glasses and laboratory glass wares were made at various proportions from 106 microns and minus 75 microns powders in combination with 5% bentonite as binder for each glass type, after several trials to determine compatibility of particle sizes. They were made using the uniaxial press at 10,000 psi and sintered at a temperature range of 700- 750oC. The results showed anisotropic shrinkage behavior for all the samples, exhibiting an axial shrinkage lower than the radial shrinkage. Sintered compact from waste drinking glass which comprised of 60% 106 microns and 40% minus 75 microns powders showed the least sintering shrinkage factor of 1.125, fused at 700oC and the highest shrinkage factor of 1.286 obtained at 750oC. This shrinkage behaviour connotes that sintering can be employed to utilize these waste glasses up to the maximum of 95% recycled glass content in ceramic tile production.

Jan 1, 2008

By Claassen J. O.

The Zinc Corporation of South Africa Ltd. (Zincor) operates an integrated roast ? leach ? electrowinning circuit. The efficient removal and control of iron forms an integral part of the process. Zincor developed its own iron removal process (Zincor Process), which was recently shown to be unique with some similarities to the para-goethite iron removal process. Newly developed operating parameters for iron removal are in the process of being implemented. These include a change in the pH-profile and operating temperature, the recycling of seed material and the utilisation of an alternative neutralising agent to aid iron removal. Some of these actions, together with the implementation of a pre-neutralisation step, new filtration equipment and control systems in Zincor?s Residue Treatment Plant have significantly reduced zinc losses associated with iron in calcine and the iron residue produced. This enabled Zincor to take a step closer to world-class zinc recovery levels of around 96% for a similar type of operation.

Jan 1, 2003

By Shufang Ding, Fukun Yan, Zhiqiang Shan, Wei Chen, Cuicui Ji

"To remove aluminum ion from chlorinated rare earth solution, this paper used hydrolysis method to explore the hydrolysis behavior of aluminum ion in aluminum chloride solution and confirm the optimum conditions of aluminum ion hydrolysis, which are pH value, temperature and initial concentration of Al203 and so on. The experimental results show that single treatment can make aluminum precipitation rates of chlorinated rare earth solution reach about 90% by hydrolysis precipitation; and then several recycle disposal can get precipitation rates of 89% for aluminum and 2.86% for rare earth.IntroductionIn China, rare earth resources are very rich and unique minerals, complete variety, and rare earth products are very large in the domestic reserves. Rare-earth and application products have been deep into all areas of our life, permanent magnet material of rare earth is one of the most popular application areas[11. Binary oxides such as praseodymium neodymium have been widely applied in the fields of glass, ceramics, magnetic materials, catalysts and so on. Especially, the advent of the Pr-Nd-Fe-B magnets which makes the world magnetic material into a new stage of development [2•3]With the development of science and technology, for industrial, physical and chemical indicators of raw materials Pr-Nd oxides (such as particle size, specific surface area and non rare earth impurities etc.) are also getting higher and higher. The oxide size has an important influence on sludge formation in the electrolytic process. If the size is too large, added oxides have settled on the bottom of slot before melting, and then generated sludge; if the particle is too small, it can cause dust dispersion, enlarge oxide unit consumption and increase the cost of production in the charging process. Some early processes use oxalic acid to make chloride neodymium praseodymium settle, and impurity can be removed cleanly, but the cost is high, it is not suitable for production. At present, most enterprises are using ammonium hydrogen carbonate to precipitate chlorinated neodymium praseodymium, but chlorinated neodymium praseodymium such as iron and aluminum and so on can easily form gel in the precipitation process, seriously affect the growth of neodymium praseodymium carbonate crystal and often leads to particle meticulous, even may also generate gel-like neodymium praseodymium sediments and cause centrifugal or suction filtration difficult. Now the actions and their removal of impurity such as iron and aluminum have done a lot of research in the production process of rare earth, removing aluminum craft with alkaline (sodium hydroxide) and acid (oxalic acid) has good effect, but the cost is higher[41; used adding complex agent to remove aluminum method which is simple and easy to operate, but aluminum removal rate is not high, and also changed the sediment of crystal type[51, and etc. This paper discusses the removal of chlorine from rare earth solution on the basis of the hydrolysis property differences betweenAJ3+ and rare earth ion."

Jan 1, 2013

By Neale R. Neelameggham

"Most chemical process plants and metallurgical production facilities have some sort of cogeneration to minimize process energy costs. Use of Alternative Energy Production from sun and wind power with storage can become an integral part of a process plant utility. This will facilitate reduced fossil fuel usage and help minimize thermal emissions. This will be similar to Pollution Control equipment, which have become an essential part of process plants in the past four decades. Conceptual flow sheets of such Process Utility schemes are presented.IntroductionPower is supplied to industries, commercial and residential users. Over the past decade, Electric Utility companies have made major inroads, in introducing alternative energy resources in an attempt to somewhat reduce fossil fuel use in power generation. Now, on a much larger scale than in the early 1980s, residential users, motivated by government provided tax credits, have started installing alternative energy generators such as roof top wind mills or roof-top photovoltaic generators. This will minimize future energy costs, help control thermal emissions etc. This alternative power generation is typically connected to the existing power grid with two way power metering. However, the use of alternative energy generation has not been seen at large industrial sites yet.Paul Scherer Institute, Switzerland and the NREL laboratories in Colorado, are two of the several institutes which have been developing how solar thermal power can be used to supply the endothermic input energy in chemical and metallurgical processes. The theme of this present symposium addresses the above as well as the energy storage needs for such events to become continuous. This paper emphasizes the concept of how alternate energy can be used in the production of materials on a generic sense wherever there is a need for input energy – beyond endothermic process energy - while addressing how to reduce the thermal and carbon emissions.The alternative energy generation using wind or solar source is discontinuous due to the nature of the energy source. They are not only discontinuous but also variable. This necessitates storage of generated power for close to continuous use with variable loads. C Smith, et al pointed out in 2006, that 'the electric power industry has taken notice of the expansion of wind and its potential' in a summary article on integrating wind generation into utility systems.1 In 2009, the 1000 MW wind generation project in Texas had to be postponed to 2013 for lack of transmission.2 There are only a few large MW solar generation units in the US; the projects being slow mainly from lack of adequate storage and redistribution."

Jan 1, 2010

By Baokuan Li, Fang Wang

"Comparing with the single electrode in electroslag remelting processes, two series-connected electrodes have the advantage of little inductance, lower power consumption and higher melting rate, which was widely used to produce superalloys and specialty steels. Detailed understanding of the electromagnetic field distribution is essential for both improving ingot quality and saving electric energy. In the present work, a 3D finite element model was developed for the magnetic field, electromagnetic force, current density and Joule heating field of electro slag remelting processes (electrode, slag and ingot) with two series-connected electrodes using Maxwell equation, Lorentz law and Joule law. The results show that the maximum current distribute occur at the middle of electrode, due to the interaction of selfinduced and mutual-induced of two series-connected electrode; associated magnetic flux density on the inner side of electrode increase and the outer decrease; The maximum joule heating is at the interface of slag and electrode. The parameter study shows that if the current frequency is greater than 35Hz, the current density in inner electrode tend to linear distribution; with the increasing of original current, The maximum current density near the wall in electrode will increase linearly; with the increasing of electrode innnersion depth and decrease of slag cap thickness and the maximum of the joule heat in slag will increase.IntroductionElectroslag remelting processes(ESR) are widely used to produce superalloys and specialty steels [l-3l_Two pair, four pair or six pair electrodes in electroslag remelting processes is common in casting large scale ingot, which has the advantage of little inductance, lower power consumption and higher melting rate, comparing to singe electrode. They have the same essence with two electrodes in ESR.Compared to the single electrode ofESR, the other electrode is added which can decrease the reactive resistance and power consumption in the two electrodes of ESR. It is a complicated metallurgy process with a series physical and chemistry phenomenon from the molten of steel to the solidification of ingot [4-71_ These physical and chemistry phenomenon originated the effect of alternating current of high intensity. The rule of the alternating current of high intensity which revealed the law of physical and chemistry phenomenon in ESR is the precondition of improving ingot quality and saving electric energy. Jihe Wei and Yongli Ren[S-9lstudied the distribution of electromagnetic field in single electrode ofESR with Maxwell equation and relative electromagnetic theory. It had the limitation that take the electrode and mold as infinite conductivity. A detail analysis of Electromagnetic fields in ESR had been conducted by Patel A D [JO-llJ using general stream-function formulation. It is difficult to extend to three dimensions which could not be used widely. Daniel V [lZJ and Kharicha A [BJ only analysis the current density associated magnetic flux density field and temperature field without the whole irlformation of electromagnetic field. Maopeng Geng [l4J considered the current density and temperature field of the real and fake electrodes in ESR without skin effect. As to the complication of the two electrodes of ESR, it is rarely reported the electromagnetic field and Joule heating field of the two electrodes in ESR. The rule of effect of electromagnetic and modification of numerical simulation should be studied in depth."

Jan 1, 2011

By Jiangtao Li, Zhongwei Zhao, Xingyu Chen, Xuheng Liu

In tungsten ion-exchange process, excessive sodium impurity enters into ammonium tungstate solution. However, the Na content of the final ammonium paratungstate (APT) product must be strictly controlled. Consequently, it is necessary to remove Na from the ammonium tungstate solution during processing in order to obtain the required purity of APT. In this study, porous Na specific absorbent, Na1+xAlxTi2−x(PO4)3, is used to remove Na from the ammonium tungstate solution. Through experiments, the effect of reagent concentration of Na1+xAlxTi2−x(PO4)3, reaction time, reaction temperature and Na concentration on the Na removal were investigated. The results showed that under optimal reaction conditions of reagent amount of NATP 1.0 times of theoretical amount, reaction temperature 25 °C and reaction time 15 min, the Na removal from commercial (NH4)2WO4 solution can reach 98%. Na1+xAlxTi2−x(PO4)3 has a good applicability to different Na+ concentrations. The obtained APT product reaches the national standard purity of zero level.

Jan 1, 2014

By Takahiko Okura, Satoshi Okano, Hiromichi Takebe

"Fine zinc concentrates tend to become sticky when roasted in a fluidized-bed reactor. The oxidation of high-purity ZnS powders and ZnS concentrates with different particle sizes were studied in terms of phase changes and particle morphologies. The sample materials were directly oxidized to ZnO in a roasting process performed over 700°C. Zinc oxide particles with diameters less than 0.5 ìðé formed at 700°C; the particle size increased by grain growth at 900°C. The coarse ZnS concentrate formed the oxysulfate ZnO2ZnS04 when roasted at 700°C; the sulfate transformed to ZnO at higher temperature.1. IntroductionRoasting is an important step in zinc extractive metallurgy because more than 80% of the world's zinc is produced from zinc sulfide concentrates using the roast-leach-electrowinning [1,2]. Currently, zinc concentrates with a finer particle size distribution are used to enhance recovery rate. However, the finer zinc concentrates tend to produce a sticky calcine in a fluidized-bed roaster [3].The factors that affect products in a fluidized-bed roaster include particle size, contaminant, O2 and SO2 partial pressures, and the feeding method of ore to the roaster. This study examined roasting behavior of high-purity ZnS powders and ZnS concentrates with different particle sizes. The phase changes and particle morphologies of the calcine samples producted from theZnS powders were studied."

Jan 1, 2012

By Alessandro Blasi, Massimo Morgana, Corradino Sposato, Pietro Garzone, Giuseppe Devincenzis

A comparison among (2-ethylhexyl)-mono (2-ethylhexyl) ester Phosphonic acid (P507), Secondary-octyl phenoxy acetic acid (CA-12) and Bis(2,4,4-trimethylpentyl) phosphinic acid (Cyanex272), in heavy rare earths separation via hydrometallurgical processes has been investigated. The separation coefficients, , were obtained and the extraction selectivity has been evaluated using a mixture of heavy rare earths from Samarium to Ytterbium. The experimental results indicated that P507 and Cyanex 272 display a greater affinity for heavier rare earths while CA12 proved to be more effective for the lighter rare earth metals.

Jan 1, 2014

By Chang-hong Peng

Solubility phase equilibrium in the ternary system of Me2+-NH4+-SO42--H2O (Me2+ represented Mn2+, Zn2+ and Fe2+) was studied by the isothermal method at 298K and physicochemical properties of the saturated solution such as density, refractive index and pH were also investigated. The experimental results show that the solubility isothermal phase diagrams of these systems consist of three invariant branches, two invariant points and three crystallization fields. Corresponding to the three crystallization fields, there have three phases of solid, that is MeSO4?nH2O, (NH4)2SO4 and (NH4)2Me(SO4)2?6H2O, respectively. At the eutectic point, the concentration and the refractive indexes of the saturated solution change evidently. Otherwise, the pH value change slowly in all the systems. The calculated results of the density and refractive index agree with the experimental results.

Jan 1, 2006

By Matti Hämäläinen

Outokumpu has developed a new chloride leaching process, HydroCopper?, for copper concentrates. The process utilizes the cupric ion as oxidant, which is able to dissolve chalcopyrite. After solution purification monovalent copper is precipitated as cuprous oxide, Cu2O, using sodium hydroxide. Copper product is produced from Cu2O by reduction, melting and casting. An essential part of the new process is chlor-alkali electrolysis, which regenerates the reagents used. All impurity metals are removed before Cu2O precipitation, because otherwise they would report to the copper product, impairing its quality. A multistage solution purification scheme has been developed consisting of firstly, chemical precipitation of impurity metals by pH increase, secondly, cementation of silver and thirdly, removal of trace multivalent ions using ion exchange. This paper describes the characteristics of solution purification in the HydroCopper? process based on the laboratory tests and pilot runs made by Outokumpu Research Oy.

Jan 1, 2003

By K. Osseo-Asare

Aqueous stability diagrams (25°C) are presented for the systems M-H2O and M-Oxalate-H2O where M=Sm, Nd, Co, and Fe. With the aid of these diagrams (i.e., Eh-pH and log[Metal]- log[Oxalate]), the solution-chemical constraints on metal dissolution and precipitation are identified. By comparing the corresponding stability diagrams, conceptual flowsheets are developed for metal recovery from Sm-Co and Nd-Fe-B magnet scrap.

Jan 1, 1997

By Michael A. Markowitz, Alok Singh

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

Jan 1, 1994