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By Guanghua Wen, Jian Li, Mingmei Zhu, Fei Xiong, Shengjian Cao

"Small inclusions removal from molten steel in a continuous casting tundish by gas bubbles, which were generated in the turbulent flow region by introducing inert gas, was analyzed theoretically and the inclusion-bubble adhesion and flotation process was also observed by high-speed photo-graph in water model. Results showed that small inclusions in the range of 20-50µm removal from molten steel by bubbles flotation involves three stages: contact, adhesion and flotation. The inclusion-bubble adhesion processes include two ways: inclusions adhering to the upper part of the bubble and inclusions adhering to the lower part of the bubble. As the bubble floats up, the number of inclusions adhering to the bubble are increased. The proper size of bubbles, which could enhance small inclusions removal efficiency, should be controlled in the range of 1-2mm.IntroductionReducing inclusions content in molten steel is a very important way to improve quality of steel, and one of the main tasks in steel making process.A variety of methods have been used for inclusions removal in molten steel. At present, the main approaches to remove inclusions are gas stirring, slag cleaning, filtering, centrifugal separating, and by means of ultrasonic or electromagnetic field. Among these techniques, gas stirring is the most widely and effectively method for inclusions removal. Inclusions in molten steel will be aggregated and generated to form larger size inclusions, and subsequently floated to the surface of molten steel by buoyancy; meanwhile, some inclusions will be adhered to bubbles and floated together to metal-slag interface where inclusions are absorbed by the covering slag layer. Some research work showed that flow behaviors of small bubbles are different from that of big ones [1-2], and smaller bubbles are more efficiency for fine inclusions removal in molten steel.There are many methods to generate bubbles. During steelmaking process, highly turbulent flow in the ladle shroud can split introduced inert gas into small bubbles, which enhances the removal of fine inclusions from molten steel. Turbulent flow of molten steel injected into tundish from ladle shroud has a high speed and it is a strong turbulent area in continuous casting. The gas can be introduced into the shroud below the slide gate. The high turbulence flow would break up the gas into small gas bubbles. Fine inclusions will be easily adhered to small bubbles and subsequently floated to the surface of molten steel. Generation of small bubbles in ladle shroud have been studied in some literatures [3-4]. Some research have analyzed the fine inclusions removal with injecting gas from the ladle shroud by mathematical simulation, and the results show that the refining method can obviously improve the removal efficiency of fine inclusions in tundish [5-8]."

Jan 1, 2013

By Jun Iwai, Osamu Takai, Yasushi Inoue, Hiroyuki Sugimura

"Infrared reflection absorption measurement was performed during plasma-enhanced chemical vapor deposition of silicon dioxide films at room temperature. Hydrocarbon contaminants adsorbed onto growing film surface are oxidized by oxygen radicals in plasma resulting functional groups which include C=O and C-O bondings. These groups exist only near the surface and are hydrolyzed rapidly after exposure to air.IntroductionRecently low-temperature silicon dioxide (SiO2) deposition has been in a growing industrial demand in pa1ticular, polymelic substrates such as polycarbonate and polyethylene telephthalate, which have poor heat resistance, need low process temperature (near room temperature) in coating of SiO2 which is a suitable material to improve optical and mechanical properties of polymenc products. Plasma enhanced chemical vapor deposition (PECVD) using organosilicon reactants is one of the most promising technique for lowering process temperature, so that it has been extensively studied1-12. In the present; however, hydrocarbon contaminants and a plenty of Si-OH termination in Si-O-Si networks tend to exist in the films, which degrade mechanical, optical and electrical properties of the films. It is necessary to understand the deposition mechanism at, low temperature in order to solve the problems. We have studied the low-temperature PECVD of Si02 by spectroscopic diagnosing techniques such as optical emission and mass analysis6-7, 11- 12Infrared reflection absorption spectroscopy (IR-RAS) has been a well-established technique for characterization of thin films on metals as· well as on semiconductors and insulators13-17. In this paper, we report on' the surface reaction of room-temperature PECVD of Si02by using in situ IR-RAS."

Jan 1, 2000

By C. Hecker, J. A. Garcia

To determine the kinetic reaction mechanism, electrochemical experimental techniques of stationary polarization, linear voltammetry and faradaic impedance were used. Gold electrodeposition experiments were realized using an electrolysis cell, provided· by a rotary disk of vitreous carbon and or' platinum counter electrode of platinum mesh and reference electrode. Using an automatic measurement system voltarnmograrns and Nyquist faradaic impedance spectra were obtained. In this paper, responses for different cases were analyzed through faradaic impedance criteria, considering several kinds of diagrams obtained. The importance diffusion influence of aurocyanide ions and adsorption as controlling steps previous charge transfer was verified. A model of proposed mechanism is discussed.

Jan 1, 1997

By Matthew Tunnicliffe, Akram Alfantazi, Paul Nesbitt, Farzad Mohammadi

"Lead and its alloys are proper candidates for anodes in electrowinning processes mainly because they are insoluble in the leach solutions and relatively cheap. However, the annual cost of corrosion problems associated with these anodes is millions of dollars. In this study lead-silver and lead-calcium anodes were tested under typical nickel electrowinning conditions and the effect of chloride on the corrosion performance of the anode materials was investigated. Corrosion rates of the anodes were calculated using the discharge plateau (reduction of lead dioxide to lead sulfate) after galvanostatic experiments. It was found that lead calcium anodes have the highest corrosion rate both in the presence and absence of chloride. Surface morphology of the electrodes was studied using SEM and the corrosion products were characterized using XRD.IntroductionLead (Pb) is usually the preferred material for commercial anodes since it is insoluble in the leach solution and the costs are manageable. One advantage of using an insoluble material as an anode is the higher purity of the cathodic deposits and better quality of the end product. During nickel electrowinning, metallic nickel is deposited on the cathode while oxygen evolution reaction (OER) takes place on the anode. In practice, relatively high potentials are necessary for the reaction to proceed at the desired rate because of the high overpotential of OER on lead. Lead anodes get oxidized in typical electrowinning conditions and usually have two to three years of lifetime. Although the price of each anode is insignificant, the overall cost of corrosion of these anodes is considerable, which is due to the large number of anodes used in a plant, typically two to three thousand. Therefore, corrosion is a significant problem associated with lead anodes in commercial nickel electrowinning plants and industries show interest in addressing this problem. Corrosion of lead electrodes in acidic environments has been previously the subject of many research studies [I-7]. It has been reported that, during the anodic polarization of lead, several phases may be present on the surface, depending on the potential range that is being studied [8]. Lander showed that lead is oxidized at potentials higher than 0.252 YsHE with tetragonal lead monoxide being the main reaction product [9]. At 0.666 YsHE lead can transform to lead dioxide; however, it is not stable and transforms to lead sulfate and lead oxide. At potentials higher than 1.684 YsHE, lead dioxide is eventually a stable phase and forms a protective layer on the surface [I 0, 11]. Under conditions of a typical nickel electrowinning plant, usually a 200 A/m2 current density is passed through the electrodes."

Jan 1, 2012

By Leah Penner, Thomas J. Ruth, Paul Schaffer, François Benard, Edouard Asselin, Stefan K. Zeisler, Thomas J. Morley

"This paper details the electrodeposition of metallic molybdenum from an aqueous, acetateelectrolyte containing molybdate ions. The deposition is carried out in a highly concentrated (up to I 0 M) acetate bath in the presence of a very low concentration of bone glue (60 µg/L). The molybdenum metal deposits are up to 20 µm thick and adherent. The deposits were characterized by XRD and XPS analysis. The deposition process is very inefficient, as up to 99% of the current is used to generate hydrogen during electrolysis. The effect of acetate concentration, pH, additives and current on the deposition efficiency and physical properties of the molybdenum deposit were investigated and optimized to obtain smooth, adherent coatings.IntroductionMolybdenum has increased thermal and wear resistance properties that are often utilized in material coatings [I]. These coatings are most often manufactured by sintering, pressing or spraying molybdenum powder at elevated temperatures, as a substitute method for standard metallurgical practices, such as electroplating [2, 3]. The lack of reports describing molybdenum deposition is most likely due to the highly oxophilic nature of molybdenum and the stability of its oxides, especially in water. Previous attempts to electrochemically reduce molybdenum from molybdate (Mool·) ions to molybdenum metal have reported the production of either a poorly adherent mixed oxide [4-6], or a thin(< 0.1 µm) metallic film [7-9]. Thick metallic molybdenum is capable of being co-deposited with one of the iron-group metals (Ni [10], Co [11] and Fe [12]) to produce an alloy [13, 14]. These alloys, however, may not be suitable for applications requiring pure molybdenum as they usually contain less than 50% molybdenum (often less than 30%)."

Jan 1, 2012

By Myung Bae Kim, Yong Hack Lee, Woll Seung Lee

The Slag Fumer is the first Ausmelt furnace system adopted at the Onsan Refinery of Korea Zinc. This plant continuously treats the QSL lead smelting slag in the molten state. It has developed progressively since its first commissioning in October 1992 and has generated a confidence that it can produce an environmentally acceptable slag for use in cement manufacture and recover the zinc and lead in the slag as a fume oxide. This paper provides the operating experiences accumulated during the last eight years of operation, a summary of problems and solutions, and the current status of the operation.

Jan 1, 2000

By Nedam Abed

A fundamental study of the sonochemical leaching of chalcopyrite in ferric ion media has been performed to understand and quantify the effects of sonication and other parameters on leaching reactions. The study covers sulfate and chloride media. The main leaching reaction: CuFeS2(s) + 4Fe3+(aq) Cu2+(aq) + 5Fe2+(aq) + 2S(s) (1) was found to be dependent on temperature and initial particle size, but less dependent on ferric ion concentration. Leaching kinetics were not affected by ferrous ion concentration or the amount of chalcopyrite added. Leaching was performed under a variety of sonication and leaching conditions. Reaction stoichiometry was confirmed through detailed wet chemistry analysis and mass balance calculations. The use of ultrasound activation showed a clear improvement in leaching kinetics and amount of copper extracted, sonication having a catalytic-like effect on the leaching reaction. Compared to experiments without sonication, reaction rates were 2-3 times faster at the same temperature, and could be faster by a factor of 20 for the same initial particle size. Regardless of initial particle size, the amount of copper extracted was comparable under sonication, and could be twice that under chemical leaching, implying the avoidance of fine particle grinding. Sonochemical leaching was found to be only temperature dependent, where the best copper extraction was at 75C. Leaching was further enhanced by the use of a grinding aid. The leaching behavior of chalcopyrite particles remained similar with and without ultrasound activation, implying that the known passivation mechanism in the oxidative leaching was not eradicated. Sonication resulted in coarse particle breakage (ultrasonic milling). Sonication did not contribute to particle passivation, as affirmed from different leaching procedures and sonication in aqueous and organic media. Parabolic leaching kinetics were confirmed for leaching experiments.

Jan 1, 2003

By M. Cloete, C. MacLagan, A. Newall

This paper initially gives a brief overview of Zinc Corporation of South Africa Limited (Zincor). The original design parameters of the Zincor roasters are compared to the current operation, and the requirements for efficient roasting are listed. Roaster operational problems experienced during the early to mid 1990's are outlined. A description of the investigation and the outcome to increase overall roaster availability are given. The history and the development of the use of oxygen at the Zincor roaster operation, with an account of the associated operational experiences, are explained.

Jan 1, 2000

By Krishna Kumar

"Growth of electronics waste (e-waste) and lack of appropriate disposal mechanism are the great concern for developing countries like India. The domestic generation of e-waste in India is rapidly growing with the development. The imported substance is also substantially contributing to the e-waste inventory. Recycling of e-waste is mainly carried out in unorganized units in India. The primitive recycling technique used by the unorganized sector is a great threat to the environment and the health of the operators involved in these profession. Therefore, improvement of technology used by these units towards a cost effective, environmental friendly alternative could be the solution to the present crisis. Few initiatives of recycling have, however, come up in recent years in organized units. The precious metals are still recycled in the developed countries. This report discusses the inventory, technology status, legal legislative and existing practices of e-waste management in India.1. INTRODUCTIONInnovation, research and development in the field of electronics and information and communication technology (ICT) lead to convenient, independent human life. Consumption of electronics and hardware products has enhanced by manifold. Electronics and hardware sectors have, thus, become the fastest growing sector in the world. Faster obsolescence of these products is forcing users to replace products with an advanced technology. Life cycles of these products are few years. Discarded electronics products are, therefore, accumulating alarmingly in our society. Electronics waste (e-waste) is a crisis not only due to its volume but also for presence of its toxic ingredients, like heavy metals (e.g. lead, mercury, cadmium, hexavalent chromium) and flame retardants such as poly brominated biphenyles and poly brominated diphenyles ether. These substances create potential occupational and environmental health hazardous."

Jan 1, 2011

By P. J. Harrington

The recovery and recycling of low concentration metal and other ions has traditionally been carried out using adsorption or ion exchange processes which, however, become uneconomical at higher concentrations, such as those that occur with many intermediate or waste streams where recycling is now being required. This paper describes the development of a process based on non-dispersive solvent extraction for the recovery of chromium (VI) from electroplating rinse water. During the chromium plating of steel, the concentration of chromium (VI) in the rinse bath rises to concentrations in the order of 100 mg/L when it becomes unusable and is then disposed of. The aim of this work was to investigate processes for recovery and recycling of the chromium in the rinse bath. The recovered chromium is required to be concentrated and purified before reuse. Tertiary amines have been shown capable of concentrating and purifying the chromium (VI) in solution. However, solvent extraction processes that have been applied to the recovery and reuse of metals from waste streams have had only limited success in the past, primarily because of the relatively high solvent losses when existing contacting equipment is used on low feed concentrations. Attempts to eliminate losses by immobilizing these complexing agents on substrates have not been successful. In order to control the losses and maintain specificity, a hollow fibre-contained liquid membrane has recently been trailed in a pilot plant to recover chromium from chromium plating waste streams. Details of the trial and modeling of the results are presented, and show that the level of losses is significantly reduced. However, issues relating to fouling still need to be addressed. This type of equipment has many applications in the recovery and recycling of a range of materials in the manufacturing processes.

Jan 1, 2003

By Yang Hai-long, FAN Gang, LI Cun-xiong, WEI Chang, LI Min-ting, LI Xing-bin, DENG Zhi-gan

Hydrothermal sulfidation of pure cerussite with elemental sulfur has been reported in the present paper. The variables considered in the study were temperature, time, particle size and elemental sulfur fraction in the reacting mixture. Temperature was the most important factor at temperatures above 180 , PbS and PbSO4 were the only stable reaction products in the sulfidation of cerussite. The experimental data indicated that under the hydrothermal conditions with a particle size of -74+58 μm and sulfur fraction in reacting mixture of 15% at 200 °C for 120 min, and 92% of lead sulfidation rate was achieved.

Jan 1, 2016

By D. G. C. Robertson

Counter-current staged reactors offer several advantages over batch reactors for mass transfer between two phases. Several metallurgical reactor designs have utilized the counter-current principle, e.g. the WORCA and QSL processes. But before the principle can be widely adopted, it will be necessary to overcome several significant problems. These include the need to minimize longitudinal mixing in a single reactor or to use several separate staged reactors and to carry out different reactions in sequence, e.g. phosphorus oxidation and sulfur reduction. Theoretical and experimental approaches to these problems will be discussed in the paper.

Jan 1, 1988

By Emanuel Negrao Macedo, Edinaldo Cunha, Mauro Oliveira, Jose Antonio da Silva Souza

"This paper presents the study of the increasing addition influence of the bauxite waste in some properties of polymeric matrices composites reinforced with natural fiber: Curaua (Ananas Erectifolius smith). There were evaluated properties as density, tensile and flexural resistances. The high pH provided by the waste is used as hydrolysis agent, providing the pectin cement dissolution of the fiber bundles, and therefore, improving the mechanical adhesion in the fibermatrix interface and the increase of the fiber bundles aspect ratio. Furthermore, the content of silico-aluminous material in the waste provides increase in the composite abrasivity, which is destined to civil and naval construction. The fact of being a low-cost and highly available waste turns the red mud in a high potential material as polymeric composite filler.IntroductionRed mud is an insoluble residue, originated from the bauxite refining through the Bayer Process [1]. It is an Iron Oxide rich material [2] (substance responsible for the red brick color), it has a complex chemical composition [3], and its composition is highly dependent of the type of bauxite used in the process [4]. It has high alkalinity (pH= 10 - 12.5) and a very small solids size distribution (95% diameter< 44µm) [1], what turns the red mud a serious environmental pollutant.The utilization of fillers on composite materials is done after many necessities; however, one of the major necessities is the cost reduction [5]. Furthermore, mechanical and thermal properties of polymers usually are improved by the addition of inorganic fillers [6], being an example of this improvement the reduction of the flammability of polymer matrixes due to the addition of functional clays [7]. In this way, the red mud becomes potential filler for composites, since cheap and easily available fillers (like red mud) are a good option to reduce costs [8]."

Jan 1, 2013

By Raymond PoIick

The Demag Electric Slag Cleaning Furnace installed at the Asarco Smelter in Hayden Arizona is one of the few rectangular electric furnaces now operating. The long transition times from charge to tap allow exceptionally clean skims (high recovery); however, the furnace design is complex. Additional Asarco requirements for rapid installation and commissioning further complicated the design. When operating and wear effects accumulated after two years of use, steps were taken to rebuild the furnace with enhanced durability based on the design parameters experience in actual use.

Jan 1, 1993

By A. V. Tarasov

In the course of research aimed at improving the performance of the Vanyukov smelting process (VP) for treating sulfur raw materials in a pilot-scale furnace it has been found that an increase in the calcium oxide content up to 12% to 14% in case of smelting to produce high-grade matte results in a decrease in the copper content of slag by 0.05% to 0.3%. The residual copper content of slag can be computed by a formula taking into account an increase in the calcium oxide content of the feed material and that in the slag. In the course of research for improving the performance of the zinc-containing slag fuming process with blowing of the slag bath with combustion products of natural gas it has been found that the silica and calcium oxide contents have an effect on the degree of zinc sublimation. In case of slag containing 24.4% SiO₂ and 6.95% CaO by weight (SiO₂:CaO = 3.51), the residual zinc content of slag was 3.25%. The minimum residual zinc content of 1.95% was obtained in case of slag containing 22.5% SiO₂ and 14.5% CaO by weight (SiO₂:CaO = 1.55). An increase in the CaO content of slag up to 16% by weight with a ratio of SiO₂:CaO = 1.25 to 1.35 permits minimization of zinc losses in slag by achieving a residual zinc content of final slag in the order of 1%.

Jan 1, 2006

By Wenbo Luo, Jilai Xue, Tiepeng Li, Jun Zhu

Sodium silicate solutions for producing silica have been ultrasound treated to enhance the precipitation process in laboratory scale. Higher precipitation rate was found with ultrasound treated solutions than those without ultrasound. The obtained SiO2 powder products were characterized using XRD, SEM, BET and laser particle size analyzer. The particle size distribution and the specific surface area of the powder products varied with the power input level and the processing time of the ultrasonic treatment. The results indicate that the efficiency of the precipitation process can be improved optimally when the ultrasound is conducted into the solutions before the nucleation stage.

Jan 1, 2015

By Gunther Klamp

Disposal of arsenic compounds from washing acid in metallurgical plants is becoming a severe problem when using lime neutralization. A further problem is the disposal of relatively large quantities of gypsum which is produced during this neutralization step and which Is also conta-minated with other toxic metal compounds. The Sachtleben-Lurgi process removes arsenic and other metals from washing acid in the form of insoluble sulphides. The purified acid contains less than 0.5 ppm of arsenic and can be used for standard sulphuric acid applications. The process Is demonstrated commercially at Sachtleben&apos;s acid plant since more than five years.

Jan 1, 1992

By J. C. Agarwal

Rare earth metal alloys are becoming increasingly important, particularly those of neodymium, because of their magnetic properties. This paper will present a generalized approach to the production economics of the metallic rare earth alloys. With appropriate regard for the chemistry of different rare earths and the large impact of economies of scale, it is possible to make fairly accurate estimates of the production costs of other rare earth alloys as well.

Jan 1, 1989

By Mark C. Bronson

The feasibility of several pyrochemical approaches-for separating non-radioactive constituents from ICPP HLW calcine were examined. The removal of aluminum as AICI3 from aluminia calcine was successfully demonstrated. The examination of pyrochemical processes to remove non-radioactive constituents, primarily aluminium, zirconium, calcium and fluorine, from zirconia calcine showed that fluorine removal was required in order to chlorinate the calcine. A molten calcium chloride wash, a calcium reduction, and. a sulfuric acid treatment were examined as possible zirconia calcine pretreatment options for fluorine removal. Fluorine removal from simulated ICPP zirconia calcine was demonstrated by both a CaCl2 wash method and a sulfuric acid treatment method. X-ray fluorescence analysis indicated that greater than 97% of the fluorine can be removed by either method. Fluorine removal by a calcium reduction using an alloying agent, zinc, or a calcium reduction using, a filtration separation were also demonstrated, but the efficiencies of fluorine removal were considerably less ranging from 50 to 90%. Regeneration of CaCl2 from the salt and oxide residues of the CaCl2 wash experiments was also demonstrated &apos;by an aqueous dissolution method. From the salt residue, 85% or more of the CaCl2 was recovered and contained little if any CaF2 or CaO. From the oxide residue close to 100% of the CaC12 was recovered. Because of the overall success of the CaCI2 wash, it was determined to be the preferred fluorine removal process. The sulfuric acid treatment to remove fluorine is effective, but the proposed overall flowsheet has not&apos; been adequately demonstrated.

Jan 1, 1995

By G. F. Archer

Selenium and tellurium, trace metals found in copper smelting, report to blister copper during smelting. Winning these metals from anode slimes, the primary commercial source, is discussed. At Asarco&apos;s Amarillo Copper Refinery, slimes treatment segregates selenium and tellurium to a water-soluble soda slag. Aqueous precipitation of tellurium oxide and selenium by sulfur dioxide is valence dependent. Se+6 and Te+6, which constitute a portion of total selenium and tellurium, are not susceptible to this base case treatment. "Secondary Selenium" is formed from these hexavalent species. We describe a process whereby simultaneous oxidation of selenium and tellurium effects a separation. Process conditions for separating selenium dioxide, and efficiency of fume capture are examined.

Jan 1, 1995