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By Liang Yu, Yuhua Li, Yuanchi Dong

"High alumina slag, with alumina normally more than 15 pct, is encountered with blast furnaces in China because of high alumina/silica ratio in iron ore as well as sinter and high ash content in coke for cost reason. High alumina slag with high viscosity and high liquidus temperature would lead to higher slag volume and thereby, furnace productivity. In the present work, liquidus temperature of high alumina slag, based on Meishan factory, Baosteel China, were investigated. A liquidus temperature model was introduced in the present work based on basic physical chemistry theory and focused on the chemical composition area used in Meishan factory(pct): Al2O3 from 14 to 17.5 and MgO from 8 to 12, so that the blast furnace slag could be designed for optimum blast furnace performance.IntroductionBlast furnace slag composition[1] has very important bearing on its physicochemical characteristics which affects smoothness of operation, slag handling, coke consumption, the degree of desulphurization, hot metal productivity and its quality etc. The slag properties which affect most are liquidus temperature, viscosity, sulphide capacity and alkali capacity. Variation of these slag characteristics with composition and temperature has been a field of active researches as these its great influence on the blast furnace operation. In the early years, most of these studies were carried out over low alumina blast furnace slags with alumina normally less than 15 pct. High alumina slag was first introduced in India because of its high alumina/silica ratio iron ore as well as sinter and high ash content in coke[2]. And then this problem becomes common as higher alumina/silica ratio iron ore imported and used [2-5]. The most important problem caused by high alumina content is liquidus temperature and then viscosity of the slag.Generally speaking those reported works [2-5] investigated a pretty wide range of chemical compositions and then obtained complex model, respectively. In fact, every factory has its own interest because of different resources. For example, the Al2O3 content from 20% to 30% pct was studied in Tata Steel India [2], but it is too high for Baosteel Meishan. A very lower percentage of alumina content, 14-18 % pct, was mainly used."

Jan 1, 2008

By Gowda H. S. Desai, A. Herbert Mervin, P. G. Mukunda

"The mechanical properties of cast iron depend on the graphite morphology and characteristics of metallic matrix. In spheroidal graphite iron these properties are affected by the nodule count, nodule percentage, nodularity, nodules per square mm, nodule types and size distribution. In this work an attempt is made to study of the effect of centrifugal and gravity casting process on the morphology and mechanical properties. A comparison of microstructure and mechanical properties of specimens of the cast are studied. It has been observed that the centrifugal effect produces an increase in rupture strain but hardness is unaffected. In microstructure it has been observed that the centrifugal effect produces an increase in the number of bigger nodules and decrease in the number of smaller nodules and an increase of nodules per square mm. It has no effect on nodularity percentage. The centrifugal casting process produces better mechanical properties.IntroductionCast iron, the first man-made composite, is at least 2500 years old. It remains the most important casting material, with over 70% of the total world tonnage [1,7]. The main reasons for cast irons longevity are its wide range of mechanical and physical properties coupled with its competitive price [l]. Gray cast iron is traditionally used in many industries because it is characterized by a flexibility of use, excellent castability, low cost, wide range of achievable mechanical properties. Gray cast irons are selected according to their tensile strength, high modulus of elasticity, good wear resistance and good machinability are desired and for this a high-strength cast iron is selected [2].Flake Graphite and Spheroidal Graphite irons are predominantly being used to manufacture heavy automobile components throughout the world. The properties of gray iron castings are much dependent on foundry practice. Perhaps the most interesting feature of the family of cast irons is the morphology of the graphite phase, which occurs as a result of changes in chemical composition, melting, melt handling techniques and the process of solidification and subsequent cooling. The significance of these differences through graphite morphology is observed primarily in their effect on the physical and mechanical properties of the iron, but in the foundries these are also known to influence the ability to manufacture sound and dependable castings."

Jan 1, 2013

By W. E. Wallace

Rare earth elements combine with most, of the metallic elements. As early as 1971 over a thousand intermetallics had been identified and described(1) From a magnetics viewpoint, systems involving. the d-transition metals Fe, Co and Ni are particularly interesting. In these systems there are at least four significant interactions: R-R exchange (R - a rare earth), R-T exchange (T = a transition metal), R-R exchange and the crystal field interaction acting upon the. rare earth ion. There is complex interplay between these interactions leading to bewildering variety in their magnetic behavior., Because of this and in view of the commercial significance of some rare earth intermetallics, studies of these systems has been an unusually active area of inquiry for the past two or three decades. The large magnetic moment of many of the rare earths, viz., 10 µB per atom for Dy and Ho, 9 1B for Tb and Er, etc., attracted, attention many years ago to the rare earths as potential ingredients for alloys to be used in permanent magnet fabrication. The utility of a permanent magnet in high perform¬ance devices (travelling wave tubes, voice coil motors, brushless motors, etc.) is in large measure determined by its maximum energy product, (BH)max. [(BH)max is the maximum value of B (magnetic induction) and H in the 2nd quadrant of the hysteresis loop.] Enhanced atomic moment in princple can lead to increased B and a large maximum energy product. Until about 1970 the largest (BH)max value known was about 5 MGOe(mega-gauss Oersted). This was for A1NiCo - an alloy involving Al, Ni and Co. It was recognized that the rare-earths had the potential for much higher energy product; in the case of Dy the theoretical energy product is about 35.0 MGOe., 70 times that of Alnico. (Needless to say, this theoretical value has never been achieved.) Large-scale efforts began about 30 years ago to synthesize magnetic materials containing rare earths and which would be suitable for permanent magnet fabrication. It was recognized by Strnat(2) et al. that a material to, be useful in high energy magnet fabrication would have to satisfy three. criteria:

Jan 1, 1992

By N. Mizutani, S. Harada, Z. Asaki, T. Tanabe

"The development of lead-free solders is urgent in view of environmental standpoints. In this -work the wettability of tin-bismuth- silver solders on copper was studied. Three kinds of fluxes were used. The wettability of conventional eutectic tin-lead .solder exhibited an excellent level over the other solders of tin-bismuth systems. Poor wettability of the tin-bismuth solders may be caused by the growth or dendritic copper-tin compounds at copper/solder interface, in contrast to the case of tin-lead'· solder. The wettability was improved by the addition· of silver in the solder. In this tin bismuth- silver system, silver was abnormally concentrated at the copper I solder interface even in the initial stage of contact. The wettability of the solder and the thickness of compound formed on the copper have a good correlation; the solder containing 2% silver exhibited the best wettability and the formation rate of copper-tin· compound on the copper was slowest.IntroductionSocial demand to avoid lead use in the industrial fields has been recently promoted· (1) because of the environmental protection of water resources. Especially the lead-bearing solders have been widely used in electronics and automobile products, and it is urgent to replace them with nontoxic materials (2)-(4). Thus the development of lead-free solders becomes an indispensable subject to the new generations and many works (5)(6) have already been carried out on the research and development of new solders. New lead-free solders are expected to have some requirements, for example, moderate melting temperature, proper strength and integrity, and lower prices, as compared with conventional solders. There have been already several alloy systems developed. Among ·these alloy systems, tin-bismuth binary or tin-bismuth-silver ternary alloys have great advantages such as having a wide range of soldering .temperature by controlling con:ipositions, though they have such disadvantages as ""lift-off"" (7)-(9): It is said, on the other hand, that a frequently overlooked property of solders, or one that is typically ignored by the research scientist as an ""issue"" for the manufacturing or product engineer, is wettability (10), although a ·work on the wettability has recently been published (11). In this Work, therefore, the authors selected Sn-Bi-Ag solders and focused mi the effect of Ag-addition to wettability of the solder."

Jan 1, 2000

By A. V. Tarasov

A flow-sheet for waste-less processing of spent lead batteries comprises mechanized separation of batteries, smelting of the metallic fraction in a kettle, electrothermal smelting of oxysulfate fraction, refining of crude lead and processing of reverts to produce commercial products. Smelting of lead-containing fraction is performed in an electrothermal furnace using a processing technology developed in the Gintsvetmet Institute and differing from conventional processes by the fact that it does not require any fluxing agent (soda); no matte is formed in the process and the amount of slag produced is minimal, because its formation depends only on the ash content of coke and the quality of battery scrap separation. The process has been patented. It has been introduced on a commercial scale in 1.8 MVA furnaces at the plant of A0 "RyazTsvetmet" (Ryazan, Russia). The process has the following main advantages as compared with conventional shaft-furnace smelting and smelting in a short-drum furnace: the process does not require technical-grade oxygen, the amount of process gas generated is minimized ensuring a decrease in lead-containing dust and sulfur dioxide emissions by 3 to 5 times per unit of lead recovered; a decrease in dust entrainment resulting in lower amounts of recycled dust; lower slag yield (a decrease from 20-25% to 3-5%); lower coke requirement (a decrease from 10-14% to 3-4%). Refining of crude lead is performed using conventional technology but there are several unique features for which know-how is available. Processing of by-products of electrothermal smelting and secondary lead refining (slag, drosses, skimmings) and ebonite fraction (crushed battery casings) is performed in a slag-fuming furnace.

Jan 1, 2002

By Ken-ichi Miyazawa

A Center of Excellence (COE) titled the Creation of Nature-Guided Materials Processing, called Nature COE, has been established at Nagoya University. In the Nature COE, a new field of material research is being developed through learning the laws of nature, namely, methods of attaining ?appearance of the maximum function under the minimum substance and energy consumption?, which the nature and living organisms have acquired through their evolution in long period. As one of the specific features, an ?Open Cluster Program? was originated for promoting the researches conducted by young researchers and Ph.D. students with those in and out of the university and also for fostering them, together with such educational programs for Ph.D. students as the research incentive, the oversea training and the international lodging seminar programs. The Open Cluster Program has been found to be effective for fostering of young researchers and students, for promoting their researches, for gathering researchers and knowledge from the world and for propagating the research fruits. Through conducting these programs, world-highest intelligent fruits and a gathering of young minds to lead the new field are expected. In this COE, the researches are conducted on (1) materials used for living bodies, (2) mimicking structures which nature or living bodies are forming and (3) materials processing by mimicking processes to form the structures observed in the nature or the living bodies. These researches are conducted by four groups to extend the processes observed in the natural world to a new type of processing that is thoroughly rationalized by plunging a scalpel of engineering, and to establish a new academic field of materials science and engineering.

Jan 1, 2006

By Ibrahim Yusufoglu, Cem Kahruman, Sedat Ilhan, Ahmet Orkun Kalpakhi

"Scheelite is the main raw material in tungsten production. In hydrometallurgical processes, extraction of tungstate ions into solution is very important. During the leaching of scheelite in oxalic acid solutions, tungsten dissolves as a chelate complex. Scheelite includes impurities along with calcium tungstate. Determination of the dissolution of these impurities is important in the subsequent tungsten production stages. In this study, scheelite was dissolved in oxalic acid solutions and the dissolution of impurities was investigated. The quantities of dissolved impurities were determined by ICP - OES and characterization of the undissolved impurities in the leach residues was carried out by SEM - EDS analysisIntroductionScheelite and wolframite ores are used for the industrial production of tungsten. Both ores are dissolved in acidic or basic solutions, and ammonium paratungstate is obtained as an intermediate product. Prior to crystallisation of ammonium paratungstate, all the impurities must be removed. Among these, Fe, Si, P, Mn, Mg and Mo are classified as ""harmful"" elements and different methods are used for their removal [1]. During purification, solvent extraction, ion exchange, etc. methods are used.Potashnikov et al. [2] studied the dissolution of scheelite in acidic solutions and the effects of stirring speed, temperature and oxalic acid concentration on the dissolution kinetics.There are no works in the literature about the removal of impurities from scheelite ores in oxalic acid solutions. Therefore, the aim of this work was to investigate the dissolution mechanisms of impurities during the leaching of scheelite in oxalic acid solutions. The effects of temperature and oxalic acid concentration on the dissolution were also investigated. In addition, the characterization of the impurities which were not dissolved was studied."

Jan 1, 2012

By Zenon R. Llanos

"The disposal of spent hydroprocessing (HDP) catalysts in the petroleum refining industry has been a concern in the past due to their classification as listed hazardous wastes. However, because these catalysts have higher metal concentrations than regular ores, and the recent surge in prices for molybdenum, vanadium, nickel and cobalt what used to be considered as a liability for generators is now viewed as a valuable renewable source of strategic metals. At the same time the generation of spent catalysts has steadily risen due to new environmental regulations for low sulfur fuels and an increased appetite of gasoline consumers. This paper will examine spent catalyst market and the role played by Gulf Chemical & Metallurgical Corporation in the reclamation of metals over the last sixty years. Introduction Hydroprocessing (HDP) catalysts are used in petroleum refineries for two main applications: desulfurization and cracking. The catalyst support is alumina or mixtures of alumina and silica. Active metals include molybdenum, nickel, cobalt and tungsten. The selection of catalysts depends on the application and sometimes the cost. The life cycle of HDP catalysts is represented in Figure 1. The catalyst cycle in a reactor varies from continuous to one-two years. Catalysts used in various refining processes are deactivated by coke, sulfur, vanadium and other impurities in the refinery feedstocks and become spent. Refineries can optionally send the spent catalysts for regeneration, metals reclamation or landfilling. Catalysts used for refining heavy crudes often can not be regenerated. Catalysts used with light oils can be reused twice or three times after regeneration. When the option for regeneration is not viable, spent catalysts are send metal reclamation facilities or landfills."

Jan 1, 2008

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 Ehsan Vahidi, Fereshteh Rashchi, Amirhossein Shahnazi

"The pig iron from steel manufacturing plants contains a high concentration of vanadium-bearing materials smelted with iron ore. During the oxidation process of the molten pig iron with oxygen lances, vanadium transfers to the slag. In this research, recovery of vanadium from LD (Linz-Donawitz) converter slag of steelmaking plant was investigated. The leaching residue was characterized by XRD and XRF techniques. The maximum vanadium recovery was achieved at optimum leaching conditions of 70 °C, S/L: 1/15, sodium hydroxide concentration: 3 M and leaching time: 150 minutes. The dissolution rate increased with rising sodium hydroxide concentration and temperature and decreasing particle size. The experimental data are treated graphically to explain the kinetics of the vanadium recovery process using shrinking core model (SCM). As a result, the controlling regimes in the SCM were analyzed separately using liquid film diffusion control, solid product diffusion control, and reaction control mechanisms.IntroductionVanadium is commercially important as a constituent of several alloys and catalysts. Nowadays, vanadium is mostly recovered as a by-product from secondary sources or from industrial waste streams such as titaniferrous magnetite, fly ash, spent catalysts, and petroleum coke. Steelmaking operations are specifically concerned by this problem due to the production of a huge quantity of by-products [1]. These by-products, including LD converter slag, sludge, fly ash, spent catalyst, ash, and alloyed scrap, contain a notable amount of heavy metals which may cause environmental problems. Solvent extraction is one of the techniques being increasingly used for the recovery of vanadium [2]. Apart from vanadium ore, secondary resources such as titanmagnetite, ilmenite and slag from the ferrous industry are a major source of supply. The pig iron from steel manufacturing contains a majority of vanadium-bearing materials smelted with iron ore. In a heat resistant shaking ladle the molten pig iron is oxidized with oxygen lances, causing the vanadium to be transferred to the slag. Normally, the vanadium in LD converter steel slag (coming from Linz-Donawitz steelmaking process) is ca. 5% as vanadium pentoxide (V2O5). This slag is the world's principal raw material for vanadium production [3, 4]. Moskalyk and Alfantazi [4] reported that a roast-leach process is used in South Africa for the production of vanadium oxides from magnetite ores while some of the slag was converted to ferrovanadium. A portion of the slag was exported to Europe for the production of vanadium oxide. The researchers mentioned that alkaline roasting was the main process at that time employed to extract vanadium pentoxide from vanadium slags."

Jan 1, 2012

By Nobuyuki Higashiyama, Ikuo Yonezu

"Hydrogen-absorbing alloys containing rare-earth elements are used in high capacity nickel-metal hydride secondary batteries,' hydrogen storage systems for portable fuel cells, and refrigeration systems. New hydrogen-absorbing alloys containing rare-earth elements have also been developed and introduced into these applications. High performance in nickel-metal hydride secondary batteries is strongly demanded because of the remarkable advancements in portable electric appliances. A large hydrogen absorption capacity, high electrochemical reactivity and superior corrosion resistance in an alkaline solution are required for hydrogen-absorbing alloys used in nickel-metal hydride batteries. The aim of this investigation is to improve the performance of conventional LaNi5 type hydrogen-absorbing alloys. For example, Mm(Ni-Co-Al-Mn)„ type hydrogen-absorbing alloys with various non-stoichiometric compositions were developed. In addition, a new process of rapid quenching process was applied for preparing these hydrogen-absorbing alloys in order to improve their performance.IntroductionRecently, the trend in electronic appliances toward portability has increased the demand for high capacity of secondary batteries as power sources. Since nickel-metal hydride batteries were first commercialized in 1990 in Japan, they have become increasingly popular as power sources for cellular phones, portable computers, electric shavers, and other, products.The performance of a nickel-metal hydride battery, such as its discharge capacity, high rate capability, and charge-discharge cycle life, strongly depends on the characteristics of the hydrogen-absorbing alloy negative electrode. Many types of hydrogen-absorbing alloys have been developed so far. For a hydrogen absorbing alloy to be used as the negative electrode material, (1) it must allow a large amount of hydrogen to be absorbed and desorbed in an alkaline solution, (2) its reaction rate should be high, and. (3) it must have long term durability under repeated charge-discharge cycling. However, LaNi5, a typical rare earth-nickel type alloy, shows significant capacity deterioration during repeated charge-discharge cycling. Therefore the first step in its development was to obtain sufficient corrosion resistance of the LaNi5 alloy for its use as an electrode material. A partial replacement of nickel with cobalt and a substitution of the lanthanum- content with misch metal (Mm), a mixture of rare earth elements such as lanthanum, cerium, praseodymium and neodymium, were very useful in improving the charge-discharge cycle life. However, the discharge capacity of the alloy was still not sufficient for a practical battery. A study of the effect of the partial substitution of aluminum and manganese showed that the best alloy composition was Mm(Ni-Co-Al-Mn)x, as follows.The stoichiometry x of Mm(Ni-Co-Al-Mn)x largely affects the discharge capacity and cycle life. Theose alloys with non-stoichiometric alloys with the compositions of [Mm(Ni-Co-AMn)x: 4.7<x<4.8] have a large capacity and a long cycle life. Nogami' et al. reported that 'a non-stoichiometric alloy with a Mm(Ni-Co-Al-Mn)x (x=4.76) composition showed approximately 10% higher discharge capacity than the stoichiometric alloy (x=5) [1] and greater influence of x on the electrochemical properties of multi-component AB„ type hydrogen-absorbing alloys for batteries."

Jan 1, 2000

By Kurt Westerlund

The design of the economically most profitable and technically most feasible smelter process gas handing and treatment as an integrated part of the total metallurgical process is discussed and exemplified, with alternative flow sheets including material and energy balances, investment and operating costs. Retrofitting and de-bottlenecking of existing gas handling lines wil1 be described and exemplified. Methods of increasing total gas handling line availability will be described.

Jan 1, 1992

By Alex Moyano

At present, the Codelco Norte smelter processes in the Teniente Converter and the Flash smelting Furnace 1,420,000 t/y of its Chuquicamata concentrate with an arsenic content of up to 1.5%. In a near future Codelco-Chile is considering different processing options for a new projected concentrates from the Alejandro Hales mine (former Mansa Mina mine with an arsenic content of up to 6%). The main option is the possibility to process 3,000 t/d of mixing concentrates from the Alejandro Hales and the Chuquicamata mines, in the Teniente Converter. The main feature of this smelting unit will be high volatilization of arsenic when processing high arsenic-bearing concentrates. The CN smelter staff carried out a technical feasibility study to evaluate the processing of high arsenic-bearing concentrates directly in the Teniente Converter, thus the low arsenic-bearing concentrates can be processed in the FSF. Accordingly, laboratory scale tests were carried out at the Tohoku University facilities. The lab-scale results allowed an industrial scale test at the Codelco Norte smelter to smelt 2,300 tpd of high arsenic-bearing concentrates in the TC and evaluate the metallurgical impact in the smelting, converting and refining areas of the smelter. The main industrial-scale result confirmed the stabilization of the arsenic content at 0.5% in the 70% Cu produced white metal at the test condition.

Jan 1, 2006

By Yongyong Gong, Qijie Zhai, Zhichen Zhang, Qixin Li, Zhishuai Xu

"Microstructure of semisolid slurry of Al-4.5wt.%Cu alloy was investigated with pulse magnetooscillation (PMO) treatment, the results showed that the PMO treatment can refine the crystal structures of Al-4.5wt.%Cu alloy significantly. The discharging frequency of PMO had a great effect on the solidified structure transformation of semisolid slurry of Al-4.5wt. %Cu alloy, and the primary a-Al particles become much finer and rounder with an increase of discharging frequency. However, over a certain discharging frequency, the grains of primary a-Al become coarse.IntroductionOver the last decade, a lot of attentions have been paid on metal rheoforming process [1-4], since it has higher mechanical properties of formed components, strength to weight ratio and age hardenablity. Nevertheless, semi-solid forming is always performed at high solid fractions (40%-60%), so it has the limitation of viscosity, a tends to be difficult to pour semisolid slurry into the hole of the shot sleeve. Therefore, a series of novel semi-solid slurry preparation methods and rheoforming techniques have been invented, such as, semisolid vibration treatment [5], rheocasting [6], pulsed magnetic field process [7], annulus electromagnetic stirring [8], via ultrasonic vibration process [9], equal channel angular extrusion (ECAE) process [l0] and straininduced melt activation (SIMA) process [11].The electromagnetic field is characterized by its effective grain refinement, green, convenient manipulation and without contamination of melt. The mechanisms of dendrite was fragmentation by electromagnetic field have also been largely proposed [12-14]. The broken dendrite arms then undergo a coarsening process to provide the globular structures and obtain much finer and rounder a-Al particles. When compared with other external electromagnetic techniques, Pulse Magneto-Oscillation (PMO) has obtained more fuvors, owing to narrower pulse width and much lower energy consumption. Furthermore, the PMO treatment can reach finer grains with shorter time treatment [16, 17]. This work aims to study the effects of different discharging frequency ofPMO treatment on the microstructure transition of the semisolid slurry of Al-4.5 wt.%Cu alloy."

Jan 1, 2014

By Michael S. Moats, Jan D. Miller, Wlodzimierz W. Zmierczak

"For many, hydrogen in a pure hydrogen economy would be like natural gas in today’s energy economy. Unfortunately, hydrogen’s physical properties are unsuited to the energy market’s requirements in terms of packaging, storage, transfer, and delivery. In this paper, a hybrid energy economy that packages hydrogen chemically on carbon atoms from various sources including recycled carbon dioxide is introduced and discussed. For this new hybrid energy economy to become a sustainable reality, the ability to recycle carbon dioxide and use hydrogen to create an appropriate energy product, such as dimethyl ether (DME), is needed. DME is recognized as a potential next generation, “beyond-petroleum”, environmentally benign commodity for energy storage and distribution. It is expected that to maximize the sustainability of the proposed hybrid energy economy, “green” hydrogen will be utilized. The “green” hydrogen would be created by the electrolysis of water powered by renewable energy sources, such as solar, wind or geothermal heat.IntroductionWith the growing concerns surrounding trends in global warming and increasing concentrations of “greenhouse” gases, such as CO2 and CH4, efforts to mitigate the emission of these gases from industrial sources are growing. With respect to CO2, the demonstrations of various capture and sequestration methods are underway around the world.The sequestration of CO2 is mainly focused on storing the gas underground or deep in the ocean. The Intergovernmental Panel on Climate Change (IPCC) estimates that 2000 Gtonnes of CO2 can be stored underground in depleted oilfields, un-minable coal beds and other geologic features [1]. Additionally CO2 may be stored at the bottom of the ocean. The lure of storing carbon dioxide in depleted oilfields or un-mineable coal seams is that an economic benefit (enhanced oil or methane recovery) can offset the costs of gas capture, transportation and storage. Unfortunately, all of these storage methods have potential for the release of CO2 or CH4 back into atmosphere or creating environmental damage (mobilizing heavy metals, disrupting deep sea ecology)."

Jan 1, 2008

By T. T. Chen

Secondary copper anodes are generally rich in Sn, Pb, Ni and Sb, but are notably deficient in Se, Te and Ag. In the secondary copper anodes, most of the Ni, virtually all of the Ag, slightly more than one-fifth of the Pb, about one-third of the As and Sb, and approximately one-tenth of the Sn are in solid solution in the copper. The remaining impurity contents occur as 1-5 µm grain-boundary inclusions in the anodes, and these are mainly Cu2O, SnO2, Cu-Pb-As-Sb-Bi oxide, Pb-Sb oxide, Sn-Ni-Zn oxide, Cu-Sn-Ni oxide, Cu-Sb-Ni oxide (Kupferglimmer) and trace Cu2(Se,Te). Barium sulphate, which originates from the mold wash used in casting, is also present in the anodes. During electrorefining, the BaSO4, SnO2, Pb-Sb oxide, Sn-Ni-Zn oxide, Cu-Sn-Ni oxide and Cu- Sb-Ni oxide inclusions are liberated and accumulate in the slimes layer. Solid solution Ni dissolves and the Ni accumulates in the electrolyte. Solid solution Sn and Pb dissolve, but partly reprecipitate as Sn arsenate and PbSO4, respectively. Solid solution Ag dissolves but rapidly reacts to form Ag2(Se,Te), Ag powder, Ag-bearing Cu2O, (Cu,Ag)SO4 or a complex oxidate phase. Partial dissolution of the Cu-Pb-As-Sb-Bi oxide particles takes place; the Pb component is converted to PbSO4, whereas Cu, As, Sb and Bi dissolve. The reacted particles retain the morphology of the original Cu-Pb-As- Sb-Bi oxide phase. Some of the solubilized As, Sb and Bi remains in solution, but much reprecipitates as SbAsO4, As-Sb-Bi oxide, and as a poorly defined oxidate phase which consists mostly of Cu-Ag-Pb arsenate-sulphate. The high Sn contents of secondary copper anodes do not seem to affect the behaviour of the anodes during electrorefining.

Jan 1, 1999

By Zhu Fangyi

"The article introduces the process EAF with De-P hot metal charging for Melting Stainless Steel in Baosteel stainless steel Branch. Based on the practice of production, the main effect on the Cr Loss during EAF with De-P Hot Metal Charging Melting Stainless Steel including using oxygen, the material charging and making slag are theoretically analyzed. The optimization of using oxygen can reduce the oxidation of Cr during EAF Melting Stainless Steel. The optimization of material charging, especially Si content is suitable can reduce the loss of Cr. Effective reduction can realize the lowest Cr oxide in slag. Based on the character of the process EAF with De-P hot metal charging for Melting Stainless Steel, applied the integrated control method, the Cr loss during EAF melting stainless steel decreased 43.10%. 1 INTRODUCTION EAF with De-P HM charging for melting stainless steel is a technology for stainless steel making. Practice prove that the new process can shorten tap to tap time, reduce the special power consumption, dilute the impurity element from the stainless steel scrap that is propitious to produce the high quality stainless steel, alleviate the shortage of stainless steel scrap to the production. As a new technology, the process has some technical problems and difficulties. The proportion of Cr alloy charging exceeds 20% during EAF with De-P hot metal charging melting stainless steel. As Cr alloy is difficult melting and easy oxidation, too much Cr alloy charging result in Cr loss too much and tap to tap time too long for EAF production. By applying the new technology, Baosteel stainless steel branch has increased the technology level and economy index. Now the content of Cr oxide in slag reduce from 8.59% to less than 6.0%. The Cr loss during EAF melting stainless steel decreased 43.10%. According to the practice application, the process of EAF with De-P HM melting stainless steel are theoretically analyzed. The main factors affecting the Cr loss during EAF with De-P hot metal charging melting stainless steel are discussed."

Jan 1, 2008

By J. G. Reid

Nickel is second only to aluminium, of all non-ferrous metals, in energy required to convert the ore to metal. Nickel Laterite ores, which constitute the feed source for approximately 40% of world nickel production, are at a particular disadvantage because of the absence of sulphur, as an energy source, in the ore and because lateritic ores general 1 y are not amenable to beneficiation. The dramatic escalation of oil prices which commenced in 1973 and continued for a decade meant that Nickel Laterite refineries using oil as a primary energy source were placed at a distinct disadvantage relative to refineries utilizing nickel sulphide concentrate feeds. By the late 1970&apos;s the continuing large difference in oil and coal prices caused Greenvale to consider converting certain high oil consuming areas of the refinery to coal. These investigations confirmed that the areas of ore drying and power generation, which together consumed 50% of total Plant oil requirements, could be economically converted from oil to coal firing. Construction of the coal conversion facilities commenced in October 1980 and the first ore drying air heater came on line in August 1981. Construction was completed with the commissioning of the coal fired boiler in June 1982. This paper outlines the additions required to receive and utilize coal in ore drying and power generation and how the changeover was completed with minimal process disruption.

Jan 1, 1988

By T. Shimizu

In Japan, the emission standard of selenium in effluent was set at a maximum of20 mgll in Feb. &apos;94 for the first time, and it is scheduled to be further decreased to a maximum of 0.1 mg/I from Feb. &apos;97 due to tightening of the Water Pollution Prevention Act. Selenium (IV) and (VI) are generally found in effluent from precious metals refineries. Although selenium (IV) can be easily eliminated by some reducing agents, selenium (VI) is more difficult to be reduced. Therefore, many smelters are having difficulty in complying with the new emission standard. At Mitsubishi Materials&apos; Naoshima smelter, the behavior and the elimination of selenium in effluent have been extensively investigated. As a result, it was found that two strategies were particularly effective. One of them is improving the overall operation of precious metals refinery, that is, feeding uniformly the effluent to the waste-water treatment plant, reducing the effluent volume by recycling and recovering more selenium (IV) in the effluent. The other is eliminating selenium (VI) in the effluent from the precious metals refinery. It was found that selenium (VI) can be effectively reduced by using hydrazine under high? sulphuric acid concentration and high temperature conditions. By using these measures, it is considered that Naoshima Smelter will be able to comply with the new emission standard.

Jan 1, 1996

By Andre L. De Vegt

For the past eight years Paques has been engaged in the development and installation of treatment systems based on biotechnological processes to remove sulfur compounds from water, air and gaseous streams. Metal and sulfate can be removed from mine waters using two biological steps: 1. Sulfate reducing bacteria convert sulfate to hydrogen sulfide (HzS). The HzS reacts with the dissolved metals to form insoluble metal sulfide precipitates. 2. Sulfide oxidizing bacteria convert excess H2S to elemental sulfur. Paques has designed and installed a groundwater treatment system for the Budelco zinc refinery in the Netherlands to remove metals and sulfate as described above. The system has been operating since May 1992 treating a flow of 5000 m3/d. A test program, utilizing a large scale pilot plant, will commence in November 1995 at a copper mine in the U.S.A. to remediate groundwater contaminated with sulfate and heavy metals. Biological reactor performance and selective metal recovery will be studied. Sulfur dioxide (S00 can be removed from fluegas using a combination of scrubber technology and the two biological steps. The end product is elemental sulfur. A commercial size biological desulfurization plant has been in operation since July 1994 treating 50,000 Nm3/h of fluegas. Sulfide can be removed from mining waters or anaerobic wetlands using a THIOPAQ® Sulfide Oxidizing reactor.

Jan 1, 1996