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By Liu Chunpeng

The new technological process developed is by means of thermal plasma arc smelting to obtain high grade Ni matte directly from Ni-Cu concentrates containing 6-7% nickel and 3-8% sulfur. In comparising with conventional smelting and converting processes the plasma arc smelting process has many advantages over conventional processes, such as lower energy consumption, lower capital investment and free from SO, pollution by transforming the sulfides into elemental sulfur with microwave irradiation under controlled oxygen potential, moreover, the process is simple and easily controlled due to less magnetite troubles in the operation. Therefore, this new technological process can be used as an alternative way to conventional process for Ni-Cu concentrate smelting. The main economical technical index is summarized in Tabal 1. Table 1 Main Ecnomic-technical Index

Jan 1, 1993

By M. Ramprecht, M. Wu, A. Kharicha, A. Ludwig, H. Holzgruber

"The influence of the frequency of AC power supply on the magneto-hydrodynamic during the electroslag remelting process is studied. The focus is on the electrodynamic field and its resulting mechanical effects on the flow and liquid interfaces. The possible influence of the electrochemistry on the droplet formation is qualitatively discussed.IntroductionThe electroslag remelting (ESR) process is a secondary melting technique which can be used for a variety of metals and alloys, provided appropriate fluxes (slags) and melting parameters are employed. The ESR process is presently operating mostly with AC current of about 50 Hz. However for reasons primarily of inductive losses in the electric circuit, furnaces for ingots larger than 1 m, use or are projected to use current of very low frequency (< 5 Hz). Effects of lower frequencies (2.5-5Hz) on macrostructure and non-metallic inclusions were recently studied by Chang [1]. Most of investigations were performed either with DC power or with AC of 50-60 Hz [2-4]."

Jan 1, 2012

By Mingming Zhang, Ramana G. Reddy

"Carbon dioxide (CO2) is one of the most common by-products produced during light metals production. It is considered to be the cause of greenhouse effects. Efficient reduction of CO2 can help minimize the rate of global warming and improving energy sufficiency. In this paper, a novel light metal production process was developed using ionic liquid electrolytes. This process has significant advantages compared to the traditional high temperature processes such as zero CO2 and CF4 emission, low energy consumption due to the low temperature operation and nonconsumable electrodes. Two types of anode materials (graphite, extruded carbon) were tested in electrolysis experiment. The results showed that both anode materials were stable (negligible weight loss). However, the extruded carbon was found to be superior to graphite in terms of current density and current efficiency. The calculated energy consumption for aluminum production was less than 10 kWh/kg at current densities up to 300 A/m2.IntroductionGlobal demand for ultra-light, ultra-strong, recyclable metals is growing as the world switches to low-emission vehicles, energy-saving devices and sustainable products. Aluminum demand is forecast to climb by 30 percent; magnesium demand by 200 percent, while for the emerging industrial light metal, titanium, the demand is expected to be at least double in the next decade. However smelting of light metals is the most energy intensive among all the steps of light metals production. For example, on an average it takes about 15.7 kWh of electricity to produce one kilogram of aluminum from alumina [1, 2, 3]. Advancements in energy efficiency have been steady, but slow, and most U.S. aluminum smelting production operates at 95% current efficiency. Besides high energy consumption, another major concern of the light metals smelting process is the emissions of greenhouse gases (GHG). Electrolysis green house gas emissions in the Hall-Héroult process can be split into three groups: 1) reduction reaction emissions, carbon dioxide (CO2) and carbon monoxide (CO); 2) process upset perfluorocarbons emissions; and 3) hydrogen fluoride (HF) formed from the moisture (H2O) present in the raw materials [2, 3]. Hydrogen fluoride gas can be captured and returned to the cells by the alumina dry scrubbing system used in modern facilities. A total of 5.31 kilograms of CO2 is generated from the reduction process for each kilogram of aluminum produced in the average U.S. primary facility. The perfluorocarbon emissions are related to the “anode effect.” If the concentration of alumina in the bath becomes too low, other reactions between the carbon anode and the bath occur and tetrafluoromethane (CF4) and hexafluoroethane (C2F6) are generated. These gases have high global warming potentials (GWP), which is a ratio developed to compare the ability of each greenhouse gas to trap heat in the atmosphere relative to carbon dioxide"

Jan 1, 2008

By R. R. Beebe

"Laboratory and pilot-scale tests are almost invariably required before metallurgical development can proceed. Difficulties with sampling, as well as with classical chemical and physical scaleups, are normally anticipated and relatively well-understood, but more subjective factors also come into play, including misunderstandings of the operating scheme chosen, wrong ""lessons"" learned from similar operations, failures to handle data appropriately, and even arbitrary intervention by management. The paper examines some of these subjective factors and suggests ways to guard against them. Several anecdotal case studies are used as examples, including when and where to heap leach or to mill specific types of gold ore.When the Romans first exploited the gold-rich gossans at Rio Tinto, they were guided by analyses and tests that delineated the ore deposits, identified the richer portions, and measured the gold recoveries achieved. There is little evidence, however, to suggest that test data were used to develop improved methods of metallurgical extraction. Indeed, it is likely that ores too difficult to treat were simply passed by, at least until improvements in full-scale operations could deal with them. For example, it is not difficult to imagine that an early metallurgist might test a tin ore by placing some in a fire; a smallscale emulation of the method actually used in practice."

Jan 1, 1997

By D. H. H. Quon

Results of a study conducted to determine the properties of iron ore pellets made from Mount Wright and Carol Lake ore concentrate fines with partial and full substitution of bentonite by several organic binders are presented. Carboxy methyl celluloses 7H and 6TL, hydroxy ethyl cellulose (natrosol) and modified guar gum all produce pellets of acceptable wet, green and dry strength. However, when fully substituted, an inorganic binder such as calcium carbonate is required for satisfactory strength development after induration. Mixing the Carol Lake ore with Mount Wright ore in a 50-50 ratio also achieves the same result. The failure of the Carol Lake ore in the pelletization process is attributed to the low hematite content of the ore. The results are very similar to those from the extrusion studies reported earlier (8).

Jan 1, 1989

By Minjun Tang, Jianfeng Zhou, Linjiang Qing, Yufeng Guo, Tao Jiang

"For the comprehensive recovery ofV, Ti, Fe in vanadium-titanium magnetite in the process of pre-reduction-electric furnace smelting, it is expected that vanadium oxide is reduced into molten iron and titanium oxide is available in the slag. Thus the effect of slag basicity, the content of MgO, MnO and CaF 2 of slag content on the separation of slag and molten iron and the comprehensive recovery of V, Ti, Fe were investigated. The results show that increasing slag basicity, MgO, MnO and CaF2 are all beneficial to the separation of slag and molten iron. Higher slag basicity and the addition of CaF2 strengthen the reduction of vanadium oxide, and inhibite the reduction of titanium oxide, which are in favour of the recovery ofV and Ti. However, the addition ofMgO, MnO was not efficient for the comprehensive recovery ofV, Ti, Fe. For the vanadium-titanium magnetite of Panxi in China, the recovery of Fe was over 98%, the recovery ofV in molten iron was over 85% and the Ti02 content in slag was about 43% under the optimal conditions of slag phase type.IntroductionIt is well known that there are abundant vanadium-titanium magnetite resources which are located in Panzhihua of Sichuan Province[!]. At present the vananium-titanium magnetite concentrates are smelted in the blast furnace, which just make use of iron and vanadium, but lots of titanium is discarded in the slag. At the same time, the process has a large number of disadvantages, such as low recovery of vanadium, long route, pollutions, large investment and expenditure of energy[2-3]. In recent years, in order to efficiently utilize the vanadium-titanium magnetite concentrates, several new non-blast furnace processes have been proposed, such as pre-reduction-electric furnace, pre-reduction-grinding separation and so on[4]. Especially pre-reduction-electric furnace is operating well in South Africa and New Zealand,However,Du to the high slag basicity of the slag, the grade ofTi02 of slag is Corresponding author:Minjun Tang.E-mail:450435123@qq.com. Tel:13627429224."

Jan 1, 2013

By Shun Fujieda, Shigeru Suzuki, Kozo Shinoda, Tetsuo Fujita

"Dowa's scorodite, synthesized by oxidation of Fe(II) ions in the presence of As(V) ions at atmospheric pressure, was characterized. The scorodite was well crystallized and had a very low solubility. To examine the conditions for stable storage of the scorodite for long periods, experiments with various synthesis and leaching conditions were done. The scorodite had a very low arsenic solubility in sea water. It was estimated in consecutive leaching tests that the arsenic concentration would eventually converge to zero. The prevention of arsenic leaching by adding goethite or ferrihydrite was limited in some cases. Very low toxicity was confirmed by toxicity tests. The investigation results suggest that disposal at a specifically designed well-controlled storage place is preferable for the scorodite whose toxicity had been made sufficiently low. Disposal to an isolated final disposal site with more stringent prevention for the outflow of toxic substances was thought another option.IntroductionArsenic is a considerable environmental concern. A system of technologies for the effective immobilization, storage and final disposal has been sought. Dowa Metals & Mining Co. Ltd. has developed a unique scorodite synthesis method (DMSP®) which works at ambient pressure [1]. The scorodite is precipitated by oxidizing Fe(II) ions in a high-concentration As(V) solution. The scorodite produced in this way does not readily release arsenic because of its high crystallinity. Final disposal is necessary because scorodite currently has no commercial value. A standard method for the final disposal of scorodite has not been established because its long-term stability under various conditions has not been fully examined."

Jan 1, 2012

By Xiaohui Li, Lianyun Liu, Hongmin Zhu, Chunfang Zi, Kai Huang, Hongjie Li

"The dissolution kinetics of steelmaking slag in pure water was studied, and the relative influential factors were investigated. The dissolution behavior of slag particles in water was well described by Noyes–Whitney equation, and for this kind of sparingly soluble rigid mineral this simple model was extensively applicable to describe their dissolution process. Experimental data were also obtained to confirm the significant promotion effect on the growth of some algae.1 . IntroductionIt has been found that the population of phytoplankton distributed in the ocean was significantly related to the concentration of some elements [1]. For example, silicon and iron were very low in the high-nitrate low-chlorophyll (HNLC) areas, which was the main factor limiting phytoplankton and other biomass growth in these open ocean surface water [7]. The silicon and iron-rich test also confirmed that the supply of these elements had the direct effect on the growth of phytoplankton processes at HNLC areas [2-8]. So in order to promote the growth of phytoplankton in these ocean areas, providing some of these elements into these ocean areas is a natural idea for choice. Steelmaking slag is a good resource for consideration because it usually contains silicon, iron, phosphorus and other elements that are necessary for the growth of phytoplankton [8-10].Haraguchi has proposed the following idea that [5-6], if steelmaking slag can be spread to the open ocean, the trace components like silicate, iron and phosphate as the indispensable nutrients for the growth of phytoplankton, will be leached into the sea water, not only promoting the growth of phytoplankton, but also making good use of these huge amount of steelmaking slag produced every year. Based on this idea, they have carried out studies in recent years and they found that silicon and iron in the slag could be extracted into seawater effectively and play a positive role in the growth process of many algae. About the dissolution of the steelmaking slag, the Japanese scholars' research work mainly focused on the thermodynamic analysis of its dissolution possibility, and in the process of dissolution they tried to adjust the pH value of the seawater by continuously adding hydrochloric acid, which was deviated from the natural conditions of dissolution, and so the laws drawn under these special conditions can not give the identical guide to the practical application. Therefore, it is quite necessary to investigate the dissolution behavior of the steelmaking slag in the seawater at the normal pH range without adjustment to simulate the dissolution possibility under the natural conditions. In the present study, the silicon extraction behavior from the steelmaking slag was investigated and the dissolution kinetics in this process was also discussed in detail. Further studies were also performed here to evaluate the promotion of steelmaking slag on the growth of algae."

Jan 1, 2011

By Tugba Basargan Çagatay Morall, Gülhayat Nasun-Saygili

"The aim of this study is to prepare the apatitic material using colemanite mineral (2CaO.3B2O3.5H2O) which was obtained from Eastern Anatolia, Turkey. For this purpose, colemanite mineral was reacted with different phosphate sources, namely, dipotassiumhydrogen phosphate, ammoniumhydrogen phosphate and ortophosphoric acid at various temperatures and time periods. Experiments were run in batch system. The apatitic material was prepared by a wet method and followed by heat treatment at various temperatures. Structure of the samples was analyzed by XRD, FTIR, XRF and SEM. The particle size analysis was also made for the result product. The experiments showed that reaction temperature, contact time and heating temperature are important parameters to transform the colemanite into apatitic structure. Reaction of colemanite with dipotassiumhydrogen phosphate and ammoniumhydrogen phosphate results in amorphous, non-stoichiometric hydroxyapatite type structure, while acid based phosphate source gives brushite and monetite type product before and after heat treatment, respectively.IntroductionBoron which has properties intermediate between metals and non-metals is a member of semiconductor group of elements. Its atom is very small and has three valence electrons. Boron exists in Earth's crust (from 5 mg/kg in basalts to 100 mg/kg in shale) and in the oceans (4.5 mg/l) [1]. Turkey has 60% of world's boron reserves which is mostly in the form of colemanite (2Ca0.3B203.5H20). Colemanite is the most important calcium containing commercial borate mineral with 5 mol of crystal water [2].Calcium phosphate cements are very useful for bone repair applications because of its chemical structure. They are injectable, easy to shape and can be maintained locally. Because of those reasons calcium phosphate cements are very effective to fill bone defects with an irregular shape [3]. Hydroxyapatite (Ca10(PO)6(OHh) is the major component of the bone (70 wt%). However, hydroxyapatite stoichiometry, composition and crystallinity differ in human skeleton system [4, 5].The main objective of the present work was to study the transformation of colemanite to apatitic material using different phosphate solutions at several time spans and temperatures. The experiments were run in a batch system, change in pH and also weight loss were measured after the experiments. Several analysis methods were used to investigate the chemical and structural changes."

Jan 1, 2012

By Steven E. Follin

In-situ leaching is commonly used to recover uranium from low-grade deposits in sandstone formations. Acceptable recovery rates can only be obtained if the formation retains its permeability during leaching. Field experiences indicate that microbial growth, stimulated by the leaching pro- cess, can cause plugging problems. To investigate this hypothesis, leach solution and solid samples from well casings and submersible pumps were obtained from four in-situ mining sites. Chemical and microbiological analyses were performed. Bacillus species, Micrococcus species, pseudomonads, and xanthomonads were isolated from these samples. A mixed culture of these organisms was inoculated into a uranium core that was being leached in the laboratory. The permeability of this ore sample decreased to one-third its original value after 16 days. The addition of hydrogen peroxide (0.2 g L-1) to the leach solution killed the microbes and restored the permeability to its original value. This suggests that periodic injection of hydrogen peroxide into production wells may reduce microbial plugging in these wells and the immediate surrounding formation.

Jan 1, 1985

By A. M. Alfantazi, M. Boissoneault, D. B. Dreisinger, J. Synnott

"The effects of five commercially available foaming reagents (range of 0 to 25 ppm) namely Dowfroth 250, Saponin, Yucca, Licorice and Meta-Para Cresol on acid mist control, current efficiency, polarization behavior, and deposit morphology and orientation were investigated. The deposition was carried out using a bench scale electrolysis apparatus (cell volume 3L) at 500 Nm-2 and 38°C for 3 hours from Kidd Creek zinc electrolyte. The acid mist control capability of the various reagents was studied and compared by characterizing the foam layer generated during actual electrowinning conditions and by direct quantitative measurements of acid mist levels on top of the electrowinning cells. Within the range considered, the addition of these reagents reduced the current efficiency, refined the grain size of the deposit, and changed to preferred orientation of most of the deposits. Among the reagents tested, acid mist measurements indicated that Licorice and Dowfroth 250 were the best acid mist suppressant at emissions of 0.30 mglm3 and 031 mg/m3 respectively while Yucca and MPC produced the most mist at 3.0 mg/m3 and 33 mg/m3 emission rates, respectively.IntroductionMost of the world's primary zinc is produced via a combined roast-Ieach-purificationelectrowinning process. Depending on the electrolysis conditions, several additives may be added to the electrolyte. Some (e.g. glue, antimony, sodium carbonate) are added to mainly counteract the detrimental effects caused by impurities while others (e.g. licorice, Saponin) are used as foaming reagents to prevent excessive acid mist formation. Acid mist emission is a problem in many electrolysis operations because it corrodes the equipment and is a health hazard to the workers in the tankhouse as well as it pollutes the environment. Due to recent trends towards more environmental protection and more stringent in-plant hygiene, there is an increasing need to minimize these aerosols. In order to eliminate or minimize these aerosols foaming agents are usually added to the electrolyte to produce a foam layer on top of the electrolyte, thus trapping most of the mist. The ideal foaming agent would trap all of the mist and would not interfere with the electrowinning process. It is also evident that the reagent toxicology, cost and availability are important factors that need to be considered.Review of the available literature clearly indicated that very little work has been done in the past on the subject of acid mist control in electrowinning operations particularly in the area of foaming and anti-misting properties of surfactants. Two papers [1,2] have reviewed briefly the existing technologies for acid mist control. Recently, most of the work in this area has focused on the development of special mechanical devices that could be attached to the electrodes and control the mist generation at the source before it is emitted to the cellhouse [2-5]. On the other hand, extensive body of literature exists that deals with the effects of anti-misting reagents on the electrowinning aspects [6-7]."

Jan 1, 1997

By Xin-liang Gao, Qing Li, Gui-qin Fu, Duo Jin, Miao-yong Zhu

"Optical microscope together with alternative wet-dry cyclic accelerated corrosion tests and XRD, SEM were employed on bridge weathering steel samples with different Mn and Ni contents which were vacuum induction melted and rolled to study their effects on the microstructure and rust layer evolution in er' containing condition. The results show that the microstructure is mainly ferrite and pearlite when Mn and Ni contents are 0.75 %, 0.42 %, respectively. Both the increase of Mn and Ni contents will make pearlite disappear while granular bainite appear, meanwhile the grain size decreases. With the increase of Mn content, the corrosion rate decreases in the initial stage, but the effect becomes little in the later stage. The increase of Ni not only improves the corrosion resistance of steel base at the initial stage but also hinders the tendency of further corrosion. As Mn content increases, a-FeOOH contents in rust layer decreases. With increase of Ni content, the content of a-FeOOH in the rust increases while that ofy-FeOOH decreases.IntroductionWeathering steels had been ~radually applied in manufacture of bridges owing to reducing the corrosion rate remarkably [I- l .Good weldability was needed for high performance bridge weathering steels. Since carbon was thought to be bad for weldability, low carbon content steel was adopted and Mn was added to amend the mechanical strength loss. Some scholars[6, 7l believed that Mn was beneficial for increasing corrosion resistance performance of the steel in marine atmospheric environment. Some scholars [S, 9l thought that Mn had little effect on corrosion resistance in marine atmospheric environment. Presently, the effect of Mn on bridge weathering steel in marine atmospheric environment still remained poorly understood. Ni was considered to be beneficial for increasing corrosion resistance performance in marine atmospheric environment [JO-l4l However, the high cost limited its application range. What would bring to the rust and corrosion by decreasing Ni content needed further research.Most researchers assumed that microstructures only affected the corrosion behavior of bare steel. But the study of Guo et al. P5l showed that the homogenous microstructures were beneficial for the corrosion resistance of steels. The effect of Mn, Ni content change on microstructure and microstructure on corrosion still remained poorly understood. In the present work, the effect of Mn and Ni on the microstructures of steel matrix, as well as the microstructures on the rust and corrosion was investigated."

Jan 1, 2014

By T. A. Venugopalan

The &apos;Hall-Heroult&apos; Process of reduction of Alumina to Aluminium has remainded basically the same for over 100 years, but the technology has been undergoing drastic changes with respect to selection of materials for Cathode and Anode, and also energy consumption. The latest generation pots have a working life of about 1800-2000 days normally. After the failure of the pots, the Cathode Lining is dug out and disposed of on land. Since the lining contains objectional materials causing pollution, various processes have been tried for re-processing of this waste. However, most of the processes have been unsuccessful from the techno-economic point of view. At Hindalco a new chemical process for converting the fluorine values of the dug out material to Cryolite was developed in 1988 and a" one ton per day Cryolite production plant has been operating since 1989. This process is especially applicable where the integrated Alumina and Smelter Plants exist side by side. The experience in operating this Plant is discussed in detail in the paper.

Jan 1, 1992

By J. R. Goode

There are at least a dozen methods of selectively removing cerium from a mixture of the rare earth elements (REE) including separation techniques based on the oxidation of cerium to the quadrivalent state. Several of the oxidation processes have been operated on a commercial scale, others have been tested and in some cases are part of proposed flowsheets. In this paper, we describe and compare the various methods. We also present preliminary estimates of the costs of early Ce removal and discuss recovery and purity aspects of the options.

By Neal Schwartz, Robert De Saro, Richard Rosenthal, Ed Kear

"A Stack Melter has been installed and is currently operating at Lexington Die Casting. The Stack Melter consists of a 1 meter (3 foot) diameter refractory tube, 2 meters (7 feet) high. Specification ingots are continuously fed to the top of the melter and piled to nearly the top. A burner fires through the scrap which melts the lower portion and preheats the upper portion. As the lower portion is melted, it is drawn out and the upper preheated scrap falls to a lower level where it in tum melts. The molten metal is fed to one of two holding furnaces for eventual delivery to a casting machine.The Stack Melter's energy use is approximately 2900 joules/g (1,250 Btu/lbm), resulting in an overall energy savings of about 58%. This energy savings is brought about primarily because the flue gases preheat the scrap and the flue gas temperature is dropped to well under 528°C (1000°F)."

Jan 1, 2000

By Katsunori Yamaguchi

The zinc, lead and alumina contents in copper smelting slag are increasing with the increase in waste recycling. The recovery of base metals such as lead and zinc from copper converter slag is important from both an economical and environmental perspective. As a fundamental study of the metal recovery by reduction process, activity coefficients of ZnO and PbO in the CaO-SiO2-FeOx-5mass%AlO1.5 slag under iron saturation at 1573K are derived from the data of slag-metal equilibrium experiments. On the basis of the obtained data, the activity coefficients of ZnO and PbO in the CaO-SiO2-FeOx-5mass%AlO1.5 slag were compared with those of the CaO-SiO2-FeOx ternary system. Addition of alumina increases activities coefficient of ZnO and PbO in SiO2 rich side of the slag, and decreases them in CaO rich side.

Jan 1, 2006

By Naiyang Ma

"High oil concentration is one of the major barriers for recycling of mill scale of steel hot rolling mills. It is of vital importance to find cost-effective technologies of reducing oil concentration in mill scale in order to recycle the mill scale without causing detrimental effects on production and environment. This paper discusses in-process separation of mill scale from oil at steel hot rolling mills. Formation of mill scale and status of oily wastewater at hot rolling mills are reviewed in the first place. A mathematical model is then formulated to relate oil concentration in mill scale to physical properties of mill scale, chemical and physical properties of wastewater and interacting parameters between mill scale particles and wastewater. From this model, three approaches of in-process separation of mill scale from oil are derived: (1) avoiding contacts between mill scale particles and oily wastewater, and (2) maintaining low oil concentration in wastewater, and (3) collecting mill scale in upper streams of wastewater flows. In-process separation of mill scale from oil might have advantages of lower capital cost, lower operating cost and less additional environmental concerns, compared to other strategies of separating mill scale from oil.IntroductionHot rolling is an inevitable step in producing finished steel products. Figure 1 schematically shows a steel hot rolling process. Semi-finished steel products, slabs here, are reheated first, and then the reheated slabs are discharged from the furnaces and transported on hot rolling trains to descaling units for removing scale with pressurized water. After being descaled, the slabs are rolled by roughing mills. After treated with cropping and the second descaling, the slabs are finally rolled into finished products, coils here, by finishing mills."

Jan 1, 2012

By Tomoya Nihei, Hiroshi Hayashi

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

Jan 1, 2008

By Uday Pal

In direct reduction processes for iron and steel making, significant amounts of Fe-C alloy droplets are generated and these remain suspended in relatively low FeO (around 5%) containing slags. Earlier workers have found that when the FeO content in the slag is <5%, the decarburization reaction becomes extremely slow (virtually ceases to occur) even though the alloy droplet contains a significant amount of carbons (2-3%). Understanding this rate controlling kinetic phenomena is crucial to designing an&apos; optimum direct steel making process. We studied decarburization of Fe-C particles by low FeO (<5%) containing CaO-SiO2A12O3 slags and found that by putting both the droplet and the slag in direct contact with an inert electronically conductive member that extends deep inside the slag bulk were able to quickly and completely decarburize the droplets. A detailed description and an explanation of the process will be presented.

Jan 1, 1995

By M. -V. Wang

Hydrotreating and hydrorefining (HT and HDS) spent catalysts contain molybdenum, vanadium, nickel or cobalt at concentration levels that can make metals recovery economically viable. Quanzhou Jing-Tai of China has developed, through many years of operating experience in metal recovery from spent catalysts, a simple process for recovery of these metals and the production of environmentally benign residues. The process first subjects the catalysts to a low-temperature calcination step, followed by grinding of the calcine. The ground material is then leached with 10-20% v/v hydrogen peroxide to recover metals such as Mo, V and Ni or Co. This step has a selectivity that is greater than 95% for the metals. The undissovled residue, which contains mainly Ah03 and Si02, can be dewaterd and used in the production of masonry bricks. The pH of the rich liquor is then adjusted to between 0.5 and 2.5 by adding dilute sulfuric acid to co-precipitate Mo and V, with a recovery rate of greater than 99%. The lean liquor contains mostly dissolved Ni or Co, which can be recovered through precipitation at a pH of between 8.5 and 9.5 by caustic additions. The final liquor is then sent to an ion exchange step for final recovery and cleanup of residual metals. The effluent is then discharged after a simple wastewater treatment process, which has been found to meet all environmental requirements. The entire process has been found to be simple, cost-effective with minimal environmental impacts while achieving the goal of complete resource recovery from spent catalysts commercially.

Jan 1, 2000