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By Eliezer Martinez-Jimenez, Gretchen T. Lapidus

"Electro-assisted reduction is an effective pretreatment to render chalcopyrite less refractory towards oxidative leaching. In this process, chalcopyrite is selectively converted to chalcocite or copper metal in an electrolytic cell under ambient conditions, while ferrous ion is leached into solution. However, the reaction velocity is hampered by the formation of a ferrous sulfide passivating layer on the solid surface, especially at elevated solid to liquid ratios. In the present work, several strategies for overcoming this problem were evaluated. On one hand, specific ligands for ferrous ion were added in order to increase its solubility and, on the other, an anode material which promotes the oxidation of the sulfide ion was chosen. Leaching tests showed citric acid to be an effective ligand for both ferrous and ferric ions and, in combination with a lead-silver anode, significantly increased the kinetics of chalcopyrite reduction and subsequent copper leaching.IntroductionAttempts to oxidize chalcopyrite at a rapid rate in aqueous solutions, below their normal boiling point, have met with difficulties because of passivation by some of its own components. An alternative line of research explores reductive pretreatment, transforming the chalcopyrite into less refractory copper phases, which can later be oxidized. A recompilation of these efforts up until 2000 was published by Dreisinger and Abed [1]. However, this practice usually requires large excesses of reducing agents, such as copper, lead, aluminum or iron, and in this last case at near-boiling temperatures, in highly"

Jan 1, 2012

By I. Iwasaki

Flotation characteristics of pyrrhotite by itself and in complex sulfide ores are reviewed with respect to the effects of oxidation, grinding media and other electroactive minerals.

Jan 1, 1988

By Mei Song, Qingyu Deng, Xuewei Lv, Lu Liu, Chenguang Bai, Meilong Hu

"The carbochlorination of several silica materials was carried out in the temperature range from 900 °C to 1200 °C. In this study, silica oxides and gaseous chlorine with carbon as reductant were used. The optimal carbon silica mole ratio in different temperature was calculated by Factsage software and the results showed that the optimal values are 1.2, 1.4, 1.6, 1.8 at 900 °C, 1000 °C, 1100 °C, 1200 °C, respectively. According to the experiments, the chlorination ratios of several silica materials were increased with temperature increasing. In the same temperature, the chlorination ratio of diatomite is the maximum and the chlorination ratio reaches 79%% when C/SiO2 reaches 3 at 1100 °C.1, IntroductionPolycrystalline silicon is the main material to manufacture the silicon polished section, solar battery[1] and high purity silicon wafers[2], also which is the most basic function material of semi-conductor industry, electronic information industry and solar photovoltaic battery industry[3]. The conventional manufacturing process of polycrystalline silicon would be divided into three parts: the improved Siemens method, which was introduced and became the main process to produce the polysilicon products in China. Silane method and fluidized bed method. Silicon tetrachloride and chlorosilans have been employed as by-products in several fields like electronic, telecounications and metallurgy[4-6]• At present, the main applications of silicon tetrachloride include production of trichlorosilane by catalytic hydrogenation, synthesis of fumed silica and ethyl orthosilicate, production of optical fiber grade silicon tetrachloride.The conventional routes for the silicon tetrachloride production have been reported, including the direct chlorination and the chlorination process of ferrosilicon, abandon catalyst and silica[7]."

Jan 1, 2013

By M. Save, N. Menad

"This paper gives the overview of different alternatives to recycle the following wastes: slag, dusts, wastes of electric and electronic equipment (WEEE) and auto shredder residues (ASR). Based on modified Bogue calculations, steelmaking slags were combined in order to produce a belite-rich clinker activated with sulphoaluminate. The EAF dusts containing significant amount of metals can be recycled in different ways: The carbothermal treatment and INTECT process are reported. The results obtained from the model of Auto Shredder Residue injection into blast furnace show that ASR can be used as reducing agent in the BF process if certain conditions are met. The particle size of this material must be controlled to ensure optimal gasification of the material in raceway. The non-ferrous contents may affect the pig iron quality, which is difficult to rectify at a later point. It seems the pyrolysis is the most attractive process to handle ASR. The BRGM flow sheet of WEEE treatment is also reported.I. Introduction The activities of human been may generate wastes and by their accumulation during several years, these wastes may have an impact on the environment and on the human health. These wastes can be generated in the forms of solid, liquid and gas. A variety of industrial wastes can be recycled for use as products. There are three ways in which industrial waste recycling occurs: at the facility itself (on-site recycling), at commercial facilities that gather waste streams from several companies (off-site recycling), and at a company that uses as inputs in its production process the waste products of another company. The industries producing iron and steel may generate different solid wastes which are classified in three main categories: 1. Ferrous material (mainly dusts and sludges from gas cleaning), 2. Slags (these by-products are generated from different process stages), 3. Others by-products (including refractories and material generated from engineering activities). According to this review, the most quantity of the metallurgical wastes is deposed. Currently, the public opinion opposes the creation of new sites. This leads to the growth of the waste disposal costs. Such situation reduces the enterprise competitiveness and decreases their market share on regional and/or national and/or world scales. In these conditions, the economical activities can be decreased leading probably to social problems. The problem of wastes and/or by-products can be treated on three levels:"

Jan 1, 2008

By Lætitia H. Delmau

SXFIT is the latest in a series of programs developed in our group to model solvent extraction systems of increasing complexity. SXFIT permits the user complete freedom to define the constituents from which the composition of each phase is to be specified in the data and from which all species of a model for a system are assumed to be formed. Activity coefficients in the nonaqueous and aqueous phases, water activity, apparent molar volumes of aqueous species, and solution density needed for the conversion of concentration from the molarity to the molarity scale are all taken into account by the program. Several extraction systems relevant to nuclear-waste treatment were modeled successfully using this program. As an example, the cesium extraction efficiency of the CSSX process chosen by the USDOE for cesium removal from high-level waste stored at the Savannah River Site can be predicted correctly for varying feed composition.

Jan 1, 2003

By Xian-Dong Zhou, Guo-Sheng Sun, Jianzhong Luo, Hong-An Guan

"Oxygen utilization rate of the pretreatment process which adopts biological contact oxidation method for slightly polluted supply water is relatively low, less than 10%, usually lower than 3%. So the aeration amount is not determined by calculated value of oxygen demand when doing process design, but by the ratio of gas and water. The aeration way of the biological pretreatment process for slightly polluted supply water was introduced in this paper. In the foundation of the principles of mass transfer kinetic theory and experimental data, the change law of DO (dissolved oxygen) and ammonia in the aeration tank was analyzed to explore aeration method which will help to improve the overall effectiveness of handling capacity.IntroductionThere are many kinds of filler used in the biological contact oxidation process, such as flexible solid filler, composite filamentous filler, powdery clay filler, particle ceramic filler and so on. Regardless of the different forms of filler, there are a couple of common points in the function of the aeration[1,2]: (1) The aeration process in biochemical tank not only provides adequate oxygen for the biological reaction, but also plays as a role of stirring water; (2) Biochemical reactions mainly happen in the upper reaches of tank, but seldom at down-streams.This paper, from the perspective of changing aeration way, discussed the feasibility of improving the effectiveness of biochemical reactions without increasing aeration amount, which would have some leading significances for the operation and management of similar projects."

Jan 1, 2008

By Fiseha Tesfaye, Pekka Taskinen

"A thermodynamic study of the equilibrium phase assemblage AgBi3S5-Bi2S3-S was made by an EMF-technique, using the RbAg4l5 solid electrolyte. The ternary phase was synthesized from the pure Ag2S and Bi2S3 in an evacuated silica ampoule and grinded into powder and mixed with appropriate compositions of B12S3 and S, in a series of experiments, for pressing in to pellets. The pellets were assembled to form the galvanic cells Pt (-) | Ag ] RbAg4ls | AgBi3S5+ Bi2S3 + S + (C) I Pt (+). The EMF-measurements were made in the temperature range 299 - 460 K.In this paper, thermodynamic functions of the ternary phase AgBi3S5 (pavonite) have been determined. The agreement between the obtained results and the literature values were established.IntroductionThe complex group of ore minerals constitutes from trace amounts to a major proportions of sulfosalts. Although the sulfosalts rarely form massive ore bodies, they are commonly associated with rich sulfide ore minerals for the base and precious metals and widely distributed in a metal poor sulfide minerals [1]. For instance, Ag-bearing sulfosalts are encountered in ore minerals for the production of the base metals and are common sources of silver. Nevertheless, thermodynamic properties of the sulfosalts are poorly known.Reliable thermochemical data are essential for quantitative modeling of the chemical behavior of the sulfosalts in equilibrium with sulfides, which in turn would promote the optimization of complex minerals treatment and extractive metallurgy of the valuable metals."

Jan 1, 2012

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

"The effects of oxalic acid concentration, temperature, stirring rate and particle size on the dissolution rate of synthetically prepared calcium molybdate were investigated. Dissolution of calcium molybdate in oxalic acid solutions takes place as a series - parallel type reaction. In the first reaction step, which proceeds according to the ""Langmuir - Hinshelwood Mechanism"", calcium aqua oxalato molybdate is formed as a complex chelate intermediate product. In the second reaction step, molybdic acid is formed during the slow hydrolysis of calcium aqua oxalato molybdate, and it reacts rapidly with oxalic acid to form the polymeric hydrogen oxalate dimolybdate chelate as an end product. Activation energies were calculated as 41.4 and 49.9 kJ mol-1 for the first and zero order reactions. The fractional conversion versus time relationship can be given by the following equation.IntroductionMolybdenum is used widely in electric-electronic, metal working, aerospace and aeronautic, nuclear, glass and petrochemical industries because of its high melting temperature and resistance against chemical effects. However, the largest molybdenum consumers are the iron-steel and super alloy industries where molybdenum is used as an alloying element. Industrially important molybdenum minerals are limited to molybdenite (M0S2), powellite (CaMo04) and wulfenite (PbMo04), which are considered as primary molybdenum resources. Secondary molybdenum resources are spent catalysts and scrap [1-4].Molybdenum has been produced by pyrometallurgical processes in the past. Since it is possible to process low grade molybdenum ores and industrial wastes by hydrometallurgical processes, which are more environmentally friendly than pyrometallurgical processes, the importance of the use of hydrometallurgical processes has increased in the molybdenum production industry."

Jan 1, 2012

By Eiki Ono, Atsushi Yamatodani, Shigeru Sunagawa, Yasushi Takasaki, Atsushi Shibayama, Yasunori Higuchi

"During metallurgical processing of non-ferrous metals, smelting residue (inc. smelter slag, flue gas and so on) is inevitably generated as secondary product.In this research, some experimental feasibilities were investigated to recover/remove Cu and As from the residue. Primarily, the removal of As and volatilized materials from the residue was examined by pyrometallurgical treatment (dry-process). In the second stage after treating the residue with a dry-process, leaching and solvent extraction as hydrometallurgical treatments (wet-process) were also investigated by using H2SO4 solution as a two stage leaching treatment, to dissolve various metals from the leach residue. Then, solvent extraction was examined by using LIX-84I as an extractant to recover and separate Cu from impurities from the final (2nd) leached solution. For the leaching stages, the removal of 90 % As and the leaching rate of 85 % Cu could be achieved by 0.25 mol/l and 1.0 mol/l H2SO4 solution, respectively. On the other hand, the extraction of over 90 % Cu and stripping was carried out by solvent extraction. 1. IntroductionIn metallurgical process for non-ferrous metals, smelting residue (inc. smelter slag, flue gas and so on) is inevitably generated as secondary product, i.e., flue dust, slug and so on. The smelting residue includes some useful metals and undesired toxic materials; Cu, Pb, Ca and As, etc.In Japan there is one undisclosed place stockpiled with 10,000 ton of smelting residue from abandoned smelters about 25 years ago. Therefore it is necessary to reduce the residual amount for space and environmental protection including water treatment by separating and removing toxic materials."

Jan 1, 2008

By E. Anelli

Based on experimental continuous cooling transformation (CCT) diagrams, an artificial neural network has been trained to predict the amount of microsturctural constituents and hardness resulting from and controlled cooling at rates from 150 to 0.015 K/s. It can be applied to quenching and normalizing processes of low-alloy steels with 0.05-0.30 C% and 0.4-2.0% Mn -with possible microalloying additions. Examples of the good predictive capabilities about 15 Vickers standard deviation for hardness and a few percent for volume fraction of phases) are reported' Keywords: Austenite decomposition, low. And medium-carbon steels, artificial neural networks

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 Yong Hwan, Wang Jian-Jun, Cai Jiu-Ju, Chen Chun-Xia

"The quantity of residual-heat and its recovery in some Chinese sinter plants are investigated. The main factors affecting energy consumption are analyzed using exergy analysis combining energy level analysis. It is indicated that the “gradation recovery and cascade utilize” of discharged gas and sinter residual heat in different temperature is the direction and the available approach to reduce energy consumption of the sinter process. Taking an iron& steel enterprise as an example, the three-ranked scheme of residual-heat recovery is put forward: ?Part of the sinter gas is used for warm-up and dryness; ?The high-temperature part of the cooler and exhaust-heat boiler are actualized as a closed-circuit, which can produce high-quality steam to generate electricity. ?The waste air in low-temperature part is introduced to sintering machine to support combustion. According to the CDQ which can recover the coal heat, the assumption of pot-recovery is put forward to replace the belt cooler. The two equipments of residual-heat recovery are analyzed in the aspect of energy consumption and CO2 reduction.1. IntroductionEnergy consumption in sintering is only inferior to iron-making in iron& steel enterprises, accounting for 10%~20% of the total energy consumption. A lot of residual heat is produced during sintering, and mostly from the sinter ore and waste gas. Sensible heat of hot sinter ore and discharged gas have accounted for 60%[1] (equals to 40 kgce/t-ore), which are the key point of sintering waste heat recovery. Discharge gas of sintering is mostly composed of flue gas deriving from sinter bed’s combustion, and the content distribution of H2O and O2 and the temperature of the gas along the length of belt-type sintering are shown in Figure1[2,3]. Currently, the sensible heat of hot sinter ore is mainly recovered by circular cooler and cooled by blasting air: the temperature of cooled discharge gas brings down from 350? to about 100? along with the decrease of sinter ore temperature. It is significant to recovery and reuse the waste heat as 4000~6000m3 discharge gas per ton of ore can be produced"

Jan 1, 2008

By Michal Rzyman, Nakamura Takashi, Shibata Etsuro, Grabda Mariusz, Oleszek-Kudlak Sylwia

"Thermodynamic considerations indicate that heavy metal oxides should easily react with HBr, the main gaseous product from the thermal decomposition of tetrabromobisphenol A (TBBPA), forming low boiling point metallic bromides suitable for volatile separation. Mechanisms and kinetics of the bromination reactions must be well recognized prior to developing of a new treatment for the simultaneous recycling of plastic waste containing brominated flame retardants (BFRs) and metal oxides (printed circuit boards, automotive shredder residue, plating sludge, metallurgical dusts). In this work, a differential scanning calorimeter and laboratory-scale furnace were used to investigate the possibility and conditions of the bromination of ZnO by product of thermal decomposition of TBBPA. The formed solid, condensed and gaseous products were analyzed by X-ray diffraction analysis, electron probe microanalysis, inductively coupled plasma analysis, ion chromatography and gas chromatography coupled with mass spectrometry. Introduction Tetrabromobisphenol A (TBBPA) is the largest volume brominated flame retardant (BFR) in production today and is used in more than 70% of the world’s electronic and electric (E&E) appliances [1]. The growth in the production of E&E products and the fact they become obsolete so quickly cause significant problems in the safe disposal and recycling of the electrical and electric waste (E-waste) and other BFR-containing waste [2]. Among various treatment processes, thermal methods are most useful since they allow the recycling and recovery of both the organic and inorganic fractions of the waste. However, incineration of the BFR-containing wastes results in the emission of hazardous organobromine compounds, while the main portion of bromine released from decomposed BFRs is present in flue gas as hydrogen bromide (HBr) [3]. HBr, which is known to damage incineration systems, seems to be a very effective bromination agent for many metallic oxides present in waste. The concept of this study is to take advantage this of its property."

Jan 1, 2008

By Michael L. Free

Bacterial oxidation of an arsenopyritic gold-ore .concentrate was carried out with continuous-flow .operation in 14-liter, mechanically agitated reactors. Samples from the slurry reactors were separated into solid and liquid fractions and analyzed separately to determine the electrochemical rates of sulfide conversion by the bacteria and the rates of direct bacterial oxidation of sulfide. The rates of the individual mechanisms are compared to the overall rates of biooxidation in the continuous-flow slurry reactors. The results show that the commonly hypothesize4 direct and indirect mechanisms of biooxidation both play a significant role in the bacterial oxidation of sulfide ores.

Jan 1, 1991

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 Toshiyuki Hashida, Victor M. Lopez-Hirata

"Small-punch tests and determination of fracture toughness JIC were conducted at 4 and 77 K on new cryogenic JN1, JJ1 and JK2 austenitic stainless steels, after isothermal aging. Equivalent fracture strain ?qf determined by measuring the reduction of thickness in the small-punch test specimen. A linear dependence of JIC on ?qf was found in these new materials. Regression analysis of experimental data produced the following linear relation JIC = 1304.1 ?qf + 8.09 [kJm-2]. An analysis of present work relation was pursued on the basis of material properties and evaluation method of he. Results showed that the slope value has a strong dependence on material yield strength and JIC evaluation method. This linear relation is useful for the evaluation of fracture toughness JIC, measuring the equivalent fracture strain ?qf by means of small-punch test. Thus it can be useful for assessing the degradation of fracture toughness in small areas such as, the heat-affected zone in welded components.IntroductionCryogenic structural materials for superconducting magnets of fusion nuclear reactor are required to possess a good combination of strength and toughness. The mechanical properties are required beyond the capability of conventional austenitic stainless steels [1]. New cryogenic JN1, JJ1 and JK2 austenitic stainless steels were developed by the Japan Atomic Energy Research Institute (JAERI) [1]. The structure of superconducting magnets is constructed by welding of 200 = thick plates of these steels, which are solution treated at high temperatures and then water-quenched to avoid intergranular precipitation. However, the welding process involves heating and cooling [2], which cause microstructural changes in both base metal and weld. In this heterogeneous microstructure, it is important to estimate the fracture toughness of these materials at cryogenic temperatures. Therefore, it is necessary to evaluate the effect of aging process on the fracture toughness behavior of these new steels. To determine the cryogenic fracture toughness, the elastic-plastic JIC value has been co=only used [2]; however, the specimen size is much larger than heat-affected zones in welded components. Small-punch (SP) testing method, employing miniature specimens, has permitted to evaluate the fracture toughness behavior at different temperatures in different nuclear reactor materials [3,4]. Mao et al. [5,6] and Misawa et al. [7] found a linear relation between JIC value and equivalent fracture strain ?qf, determined by SP method in non-ferrous alloys and ferritic steels at room temperature and austenitic stainless steels at 4 and 77 K, respectively. So that, this kind of correlation would be very useful to assess the fracture toughness JICe values by means of SP test in small zones of welded components."

Jan 1, 2012

By F. G. Caballero, J. L. Gonzalez-Carrasco, S. Barrius, H. Carreon, M. Lieblich

"The grit blasting is a low-cost technique successfully used to enhance mechanical fixation of the implants through increasing their roughness. As a result of the severe plastic surface deformation, it produces subsurface effects such as grain refinement, hardening and compressive residual stresses which are generally evaluated with destructive techniques. In this research work, non-contacting and contacting thermoelectric power measurements are performed in blasted 316L VM and Ti-6AI-4V specimens using Ah03 and Zr02 particles which yield a coarse and a fine rough surface, respectively. This study correlates the microstructural changes induced by the grit blasting treatment and the limitations and advantages of each of the nondestructive thermoelectric techniques based on the Seebeck effect used to evaluate these biomaterials.IntroductionIt is well known that surface properties play an important role in metallic materials used in bio-medical applications. Since the biological response is correlated directly with surface properties it is comprehensible the intense activity in superficial modification by physics or chemistry methods in this field. Grit blasting, one of the most popular surface modification of metallic biomaterials, enhances the mechanical fixation of the implant through the increase in roughness [1-3]. Roughening is developed by bombarding the surface with a high-velocity jet of ceramic particles, being the final roughness a function of the processing parameters (pressure, distance, time, ... ) and blasting particles (nature, shape, size). As the plastically deformed surface layer tries to expand relatively to the intact interior of the specimen, residual compressive stress gradients develops perpendicular to the surface at shallow depths with a maximum value at a depth in the range of 5 to 60 µm. This surface treatment also may cause subtle variations in the subsurface material properties, such as increased hardness and grain size refinement, which are consequences of the significant plastic deformation through cold work. Blasted affected zones may extend to a depth of up to about 200 µm. The subsurface hardening and the near-surface compressive stress gradient playa beneficial role by retarding fatigue crack nucleation and further growth, ultimately extending the fatigue life of the metallic part [4]. In this work, two non-destructive thermoelectric techniques (NDTT), the non-contacting and contacting thermoelectric power measurements were used to analyze the subsurface induced changes on blasted Ti-6AI-4V and 316L VM specimens using Al2O3 and Zr02 particles. Detailed information on the microstructural induced effects and subsurface mechanical properties were published elsewhere [5-8]. Here the nondestructive evaluation of the involved microstructural changes is used to assess the global subsurface damage. Advantages of using nondestructive techniques during manufacturing are envisaged."

Jan 1, 2012

By Ray Y. Lin

Chemical vapor deposition of tungsten carbide on the surface of steel has been investigated at temperatures between 400 and 550C in an atmosphere containing tungsten hexafluoride, hydrogen and benzene. The tungsten fluoride flow rate was maintained at 20 ml/min. The hydrogen flow rate was at 100 ml/min. The benzene concentration varied from 1.15 to 5.56% in the reaction gas. It was observed that the higher the temperature, the faster the deposition rate for tungsten carbide. But the dependence of the deposition rate on the benzene concentration was not systematic. From the x-ray diffraction analysis, it was observed that W, W2C and WC are all presented in the coating. The amount of each phase presented in the coating depends on the temperature and, to a less extent, on the benzene concentration. The microhardness measurement has also been done for all CVD carbide coatings obtained in this study.

Jan 1, 1992

By P. Klut, D. Groult, R. Marechalle, B. T. H. Bonnema

In the past 5 years, Compagnie Europeenne de Dezingage (CED) has developed a successful dezincing process and the St. Saulve pilot plant has evolved into a commercially successful production plant. Currently the plant meets all the required standards for scrap and zinc quality, output capacity, availability, and meets the prescribed environmental emissions standards. The initial process problems relating to zinc recovery, uncontrollable explosions and sodium hydroxide aerosol emissions have all been solved. Presntly, the yearly production of dezinced scrap is around 50.000 tonnes/year; this capacity is enough to supply the local market. This capacity can be increased easily to 65.000 tonnes/year or more. The market for dezinced material is growing due to the increased consumption of galvanized material on one hand and on the other hand the higher demand for high quality scrap. The proven technology of CED is currently patented worldwide, but CED is inviting licensees to implement the dezincing technology in other parts of the world.

Jan 1, 2000

By Jason Graetz

Aluminum hydride is a covalent, binary hydride that has been known for more than 60 years and is an attractive medium for on-board automotive hydrogen storage, since it contains 10.1 % by wt. hydrogen with a density of 1.48 g/ml. There are at least 7 non-solvated AlH3 phases, namely a, a', a, ?, d, e and ?. The properties of a-AlH3, obtained from the Dow Chemical Co. in 1980, have been previously reported. Here we present a description of the thermodynamic and kinetic properties of freshly prepared a, 0 and y phases of AlH3. In all cases the decomposition kinetics are appreciable below 100" C and all will meet the DOE 2010 gravimetric and volumetric vehicular system targets (6 wt% H2 and 0.045 kg/L). However, further research will be required to develop an efficient and economical process to regenerate AlH3 from the spent A1 powder.

Jan 1, 2006