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Primary sulphidic gold ores in the Archean provinces of Western Australia can be broadly sub-divided into pyritic, pyrite-telluride, arsenical and antimonial types. Pyritic ores contain only native gold, and are essentially not refractory. Arsenical ores almost always carry some invisible gold, and may vary from mildly to highly refractory. Pyrite-telluride ores contain gold-bearing tellurides, and are refractory to varying degrees. Antimonial ores usually contain aurostibite, and may be very difficult to process. A classification scheme for metallurgical processing, based on mineralogy, is proposed for the ores, and implications for processing are discussed.

Jan 1, 1995

By S. Street

The Environment process, invented by Prof. H.K.Womer and developed at the University of Wollongong, simultaneously treats ferruginous and organic wastes via bath smelting. Conceived in the late 1980's, the patented process was originally developed using steelworks dust to settle solids from sewage, producing a composite material suitable for smelt reduction. Work began on the process in 1990 with the Australian patent having a priority date of February 1990. Early research focussed on settling of solids from sewage, while pyrometallurgical investigations examined smelting in small induction furnaces. By 1992 smelting trials had been undertaken in pneumatic and electric arc furnaces, the process being successfully demonstrated up to on 8 tonne scale. The success of this particular trial, and other smaller trials, resulted in construction of a 100kg DC arc furnace which was commissioned in 1993. By 1994 the main project focus was on development of the smelting technology. Over 3 years of trials on the DC arc furnace have identified and clarified many of the pyrometallurgical reactions. optimum operating parameters, as well as demonstrating the versatility of the process for treating a wide range of wastes. Currently the Illawarra Technology Corporation (lTC), the commercial arm of the University of Wollongong, is pursuing commercialisation of the process.

Jan 1, 1996

By Sylwia Zymankowska-Kumon, Rafal Danko, Józef Danko, Mariusz Holtzer

"Burning of ceramic materials is carried out at temperatures 900+ 1300°C, in dependence of the required functional properties. The Faculty of Foundry Engineering together with the Faculty of Material Engineering and Ceramics developed the technology of production of burned ceramic materials with using spent moulding and core sands. The mentioned above waste materials of the foundry industry fulfilled -in plastic masses intended for obtaining ceramic materials -the role of the addition weakening clay raw materials. The laboratory investigations were fully verified by the results of industrial tests. It should be pointed out that none negative effects were observed at the stage of mixing raw materials and preparation of plastic masses. The measurements of exhaust gases emissions performed during burning the products containing spent moulding sands as well as during the normal production did not exhibit any significant differences, which could have indicated the harmful impact on the natural environment.IntroductionSands are used by the foundry industry to make metal casting molds and are a mixture of silica sand, bentonite clay and carbonaceous additives or resins. During the casting process, the molten metal cause thermal decomposition of carbonaceous additives or resins, which results in the formation of potentially hazardous organics, that are emitted to the atmosphere and condense in the molding sand. Each year the U.S. foundry industry landfills about 10 million tones of sand because it is no longer suitable to make metal casting molds. A large high-silica sand content in spent foundry sands (SFSs) generates rational premises for their reuse in other than foundry practice fields. Efforts to divert the SFSs from landfills and encourage their beneficial use in manufactured soils, geotechnical applications, the construction industry (road construction, highway construction), the building materials industry (cement, bricks, limestone manufacture), in the filling of mining cavities or in landfill construction (roads on landfills, permanent covers) are make [1-7]."

Jan 1, 2013

By James J. Komadina, Robert R. Beebe

"Heap leaching of gold ores has enjoyed wide acceptance in the arid and semi-arid regions of the western U.S., Australia and South America. There are areas, however, where cold weather or excessive precipitation can limit the usefulness of heap leaching. Even in Nevada difficulties can be encountered which call for special operating procedures.The paper discusses the general climatological limitations and some of the techniques used to extend heap leaching into colder conditions. A case history of the Cripple Creek and Victor Gold Mining Company operation in Colorado examines 'valley-fill"" technology as an ideal cold-climate solution, where topographical conditions permit.AcknowledgementsThe authors gratefully acknowledge the management of Independence Mining Company for their permission to present this paper. The contributions of Golder Associates; Pikes Peak Mining Company Environmental Affairs Department staff, and the Colorado Department of Mines and Geology were all invaluable in successfully concluding this project.BackgroundWhen heap leaching of oxidized gold ores was introduced in the rnid-1970s it was aimed at large tonnages of low-grade material which could not, in general, be developed via conventional milling. Normally, the reasons for this were economic rather than technical: capital and operating costs for milling were simply too high. At first, grade was almost the only criterion, but deposits too small to justify milling were also potential targets for heap leaching.Renewed interest in gold was centered in the western United States and Australia, where exploration for milling-grade deposits had never really died. When heap leaching came along, it was in these areas that the first developments took place. Coincidentally, these same areas were favorable for heap leaching: climates were temperate for most of the year and competing land uses were limited. Even so, in the western United States in particular, winter temperatures were low enough to complicate operations. Precipitation was less a problem, although heavy snowfalls could periodically interfere as well."

Jan 1, 1997

By V. A. Luganav

The behavior of arsenopyrite under heating has been studied by many scientists. It has been already established that under heating at more than 650°c and without air access the arsenopyrite dissociates with the formation of one atom arsenic. Under vacuum the dissociation process begins at 5500C with the formation of elemental arsenic. The residue of dissociation process contains pyrrhotite and throilite. In the presence of pyrite, arsenopyrite dissociates under lower temperature and with a higher velocity than without it. The industrial realization of fool scale processing of arsenic bearing raw materials is possible only by the use of standard equipment and oxygen containing blast. In this view the paper presents the results of the study on the effect of oxygen in the gaseous phase and its addition into the charge of pyrite in the process of arsenopyrite decomposition. Thermodynamic analyses showed that under thermal processing of arsenopyrite in the presence of pyrite and limited quantities of oxygen in the gaseous phase the formation of arsenic sulfides is possible according to the following reactions:

Jan 1, 2003

By Sheng-li Wu, Guo-liang Zhang, Bo Su

One of the major challenges for the Canadian Gen IV Super-Critical Water-cooled Reactor (SCWR) concept is the selection of fuel cladding materials. The Canadian SCWR concept will operate at a core outlet temperature of 625 oC and 25 MPa of pressure with peak cladding temperature reaching as high as 800 oC. Corrosion resistance is an important factor for material selection. Austenitic stainless steels that contain Cr contents greater than 18 wt.% are generally considered to provide adequate corrosion resistance. In this work, the pressure dependence of the corrosion of austenitic stainless steel 310 containing 24 wt% Cr is assessed at 625 C for exposures of 1000 hours to evaluate the suitability of superheated steam as a surrogate for supercritical water at 25 MPa. Transmission Electron Microscopy (TEM) revealed that 310 exposed to different pressure conditions at 625 oC. (i.e., 0.1, 8 and 29 MPa) had generally the same type of the oxide structure, i.e., a Cr-rich oxide with the spinel structure on outer surface adjacent to the water phase. The material exposed at 8 and 29 MPa had a double layer oxide structure, with the outer oxide layer having a much larger grain size, while the samples exposed at 0.1 MPa showed only a single spinel-phase oxide layer. Cr-depleted recrystallized austenite grains were found underneath the spinel phase oxide. The adjacent large-grained austenite substrate had M23C6 carbides in the grain interior. The implications of these results are discussed.

Jan 1, 2015

By Dhanesh Chandra

Metal carbonyls are of great importance in chemical vapor deposition (CVD), composite materials fabrication, and other near-net shape technologies. Carbonyl CVD application applies to deposition of high-purity metallic/alloy coatings. Vapor pressures of solid Os3(CO)12,Rh6(CO)16, Ru3(CO)12, Ir4(CO)12, Re2(CO)10, Co2(CO)8, Cr(CO)12,, and W(CO)6carbonyls have been measured using gravimetric-torsion effusion system. The vapor pressure data is used for many low and high temperature CVD applications. Interesting decomposition/disproportionation vaporization behavior has been notedfor Rh6(CO)16, Ru3(CO)12 and Co2(CO)8. The vaporization studies of Rh6(CO)16 showed virtually complete decomposition to Rh metal and the measured molecular weight of the effusing gas from the solid Rh6(CO)16 was 27.75 g/mol, close to that of carbon monoxide as compared to 1065.56 g/mol for the value of solid Rh6(CO)16. Electron microscopic characterization, X-ray line broadening results for Rh carbonyl has been performed on the vaporization product. However, Ru3(CO)12, Co2(CO)8 showed very complex behavior. The molecular weights of the vaporizing species have been estimated and the numbers of vaporizing species are proposed. For example, there was partial decomposition of Ru3(CO)12to(approx. 52%) metallic Ru and CO gas during vaporization, as suggested by the difference in the molecular weight of the vaporizing species of 107.58 g/mol compared to the actual value of 639.33 g/mol. The dimer Co2(CO)8 partially disproportionates to tetramer Co4(CO)12, monomer Co(CO)4, and CO gas. Whereas, the Os3(CO)12, Cr(CO)12,, and W(CO)6have shown virtually no disproportionation. The total vapor pressures of all the above-motioned carbonyls, partial pressures of various species, average molecular weights of the effusing gases, equilibrium constants for the vaporization reactions, their enthalpies, entropies, and Gibbs energies will be presented.

Jan 1, 2006

By Claudio Toro, Alex Moyano, Jonkion Font, Carlos Caballero, Pedro Morales

"Codelco-Chile in the last decade has carried out industrially-oriented research as an alternative to the traditional batch-type converting process. In a first stage carried out preliminary evaluations in a rearranged Peirce Smith (PS) converter, and then an exploratory test in a “Convertidor Teniente” (Teniente converter, TC) for the Codelco-Chile Continuous Converting Process. However, the validation test for this process in the TC was delayed up to the second quarter of 2007 where the validation studies were done satisfactorily.Thus, the objective of this paper is to present the results of the campaign tests validating the Codelco-Chile Continuous Converting Process in the TC1 of the Codelco Norte smelter.The results of charging the solid or liquid matte or high grade matte (“white metal”) by Garrgun, or by mouth of the 22 m x 5 m TC1 are presented. Some features of the industrially validated process are discussed, and the pilot test results of the matte injection are also presented."

Jan 1, 2009

By Ningchuan Feng

A biosorbent, the chemically modified orange peel, was prepared from hydrolysis of the grafted copolymer, which was synthesized by interacting methyl acrylate with cross-linking orange peel, and FT-IR spectroscopy was used for determining the structure of the biosorbent. Adsorption characteristics and effects of various factors of the biosorbent on Cu (II) were investigated including pH, adsorption time and initial concentration of Cu (II). Experiment results show that when pH was 6.0 and the initial concentration of Cu (II) was 50mg·L-1, the removal rate was 91.7% after 3 h adsorption. After four cycles being reused, 85.3% removal rate could be obtained by the biosorbent.

Jan 1, 2008

By Aichun Dou

Au-Sb alloy sample in which the total amount of Cu and Ni is below 25% (wt. %). In practice, Cu and Ni were difficult to be dissolved in sulphuric acid solution by oxidative leaching under the atmospheric pressure conditions, because of the lower concentration of Cu and Ni in the sample. In this paper, pressure oxidation leaching in sulphuric acid system (POLS) followed by hydrochloric acid leaching (HAL) was employed to remove impurities in the Au-Sb alloy. The effects of variables in POLS on leaching ratios of different metals were investigated in detail. Under the optimal conditions: the concentration of H2SO4 is 1.5 mol/L, liquid-solid ratio is 7:1, the amount of oxidizer is 1.2 times of the theoretical amount, leaching time is 4h and leaching temperature is 427K, the leaching ratios of copper and nickel reached up to 99%, antimony, lead and silver were not dissolved in dilute sulphuric acid solution. The residue from POLS was then treated with hydrochloric acid solution in fixed conditions, the leaching ratio of antimony reached over 92%, the grade of gold in the ultima residue was enriched up to 66%.

Jan 1, 2016

By Hector M. Henao

In order to provide the thermochemical data regarding the slag system, which are of importance for sulfide smelting and metallurgical processes but still lacking, an experimental study was carried out on the phase relations and activity of iron oxide in the FeOX-CaO-SiO2 system at temperatures between 1300 and 1400 °C and partial pressures of oxygen between 10-9 and 10-4atm. First, the solubility of CaO and SiO2 in the solid FeO were obtained and the tie lines connecting between the solid wustite (FeO) or magnetite (Fe3O4) phase and the liquid phase were determined. Secondly, iso-activity lines for FeO in the homogeneous liquid region were determined, based on the activity of iron in the Pt-crucible used in the equilibrium experiments. The activity coefficient of FeO in this region was also derived from the composition of FeO and FeO1.5 in the liquid region. Finally, the effect of (CaO/SiO2) ratio in the system and partial pressure of oxygen on these thermochemical quantities is discussed.

Jan 1, 2006

By Zizheng Zhou

The separation of cobalt from other base metals can be achieved using diffusion dialysis in a two-compartment reactor separated by an anion exchange membrane. In this work, a Neosepta AFX membrane was used to study the separation of various metals in an acid-chloride solution. The separation of one metal from another was investigated on the basis of the various chloro-complex stabilities. The metals investigated included cobalt, nickel, copper(II), iron(III), aluminum, zinc and cadmium. The impact of several critical experimental conditions, including the initial metal and chloride concentration in the feed solution and their initial concentration in the receiving solution, on the separation factor and the metal transfer rate is reported in this work. Effective separation of different metal pairs was achieved under the experimental conditions.

By John A. Herbst

Plantwide control of mineral processing operations has long been sought for its potential benefits. These benefits include minute-to-minute optimization, reacting to disturbances in ore characteristics and equipment status as they happen and the coordination of all unit operations in pursuit of the highest performance level. However several difficult challenges have kept us from fully realizing those benefits. One of these challenges has been to provide fairly complete quantitative descriptions of Unit operations to account for critical interactions within and 'between unit operations. In some cases we understand the physics and chemistry very well and can incorporate that 'knowledge into phenomenological models. In other cases our knowledge is incomplete, so we must rely on other forms of knowledge such as fuzzy logic or neural nets. Another challenge to be met has been to simultaneously compute a large number of manipulated variables. In the past this challenge was met by optimizing only unit-by-unit, rather than on a global basis to significantly reduce the number of variables. In this paper, a procedure that globally optimizes one or two important variables is outlined. This procedure comes much closer to true plantwide optimizing control while remaining computationally feasible. Finally, another major challenge is to choose a meaningful global objective that can be calculated With the models and can be effectively optimized. Financial goals seems to be the objectives of choice. This paper discusses recent progress In overcoming the challenges and illustrates a promising approach which is being pursued at :Mexicana de Cobre's 'La Caridad copper ore concentrator. At M de C, advanced ,control strategies have been 'installed one at a time in the crushing, grinding and flotation sections. During this period, the throughput of La Caridad, Mexico's largest copper concentrator, 'increased from 76;000 tpd to 90,000 tpd. Plantwide integration is expected' to gain an additional 3% improvement in profitability.

Jan 1, 1996

By Kenji Morinaga, Shigeru Fujino

"Preparation and vacuum ultraviolet (VUV) transmission spectra of aluminum fluoroberyllate glasses, MgF2-CaF2-SrF2-A1Fr BeF2 (MCSA-Be) and MgF2-CaF2-SrF2-AlFrYFrBeF2 (MCSAY-Be), were studied. The influence of YF3 and BeF2 on the thermal stabilization against crystallization and VUV transmittance was investigated. With increasing the BeF2 content, the crystallization tendency decreased and the absorption edge shifted to shorter wavelength in the MCSA-Be and MCSAY-Be glasses. The MCSA-20Be glass composition exhibited the shortest wavelength UV absorption edge (-147 nm) and the highest transmittance at 157 nm (60% for 2 mm sample thickness). The transmission values at 157 nm and the slope (steepness) of the absorption edge were found to be significantly influenced by the trace amount of Fe2+ derived from the BeF2 raw materials.IntroductionPure beryllium fluoride is known to be an only fluoride that forms one component glass on cooling from the molten state and is structurally similar to silica with [SiO4]4- tetrahedra. Molten BeF2 is highly viscous with a viscosity of about 106 poise near its liquidus temperature at 550""C[l]. The addition of modifying fluorides such as LiF, NaF or KF to BeF2 substantially decreases the viscosity[2]. Glass forming region of binary fluoroberyllate glasses has been mainly reported by several authors [3]. LiFBeF2 binary system is structually analogy for Mg0-Si02 system from their phase diagram and ratio of ionic radius for each cation and anion, respectively. LiF-BeF2 binary glasses seems to be promising candidates for the extreme deep vacuum ultraviolet (VUV) transmitting optical materials owing to their larger band gap. However, it is chemically unstable, and so, have no practical application for lens systems in micro lithography equipments and substrate materials for F2 (157nm) excimer laser[4]. There are also few reports on the VUV transparency of multicomponent aluminium fluoroberyllate glasses from the view point of their compositional dependencies. The purpose of this paper is to prepare deep VUV transmitting optical materials and determine the optimum glass compositions for aluminium fluoroberyllate glasses investigating their thermal stabilization against crystallization."

Jan 1, 2000

By T. V. Jayaraman, D. Das, B. Mallesham, A. R. James

The PNN-PZT xPb(Ni0.3Nb0.67)03-(1-x)Pb(Zr0.31 Ti0 69)03 (0.2=x=0.6) based relaxor-ferroelectric material was synthesized by colurnbite precursor (NiNb206) method via conventional solid state reaction. Homogeneous mixture of required oxides and precursor was calcined at 850°C for 4 hrs to obtain phase pure perovskite. Pellets of PNN-PZT ceramics were sintered at 1100oC for 4 hrs. Phase pure perovskite structure was confirmed by the X-ray diffraction analysis. From the X-ray diffraction analysis it is also confirmed that there is a structural transformation from the rhombohedral to tetragonal with increase in PZT content and existence of morphotrophic phase boundary (MPB) at x = 0.5 composition. The morphology and microstructure of the sintered pellets were observed using the scanning electron microscope. P-E loop measurement shows the high remnant polarization (19.12 µC/cm2) and low coercive field (6.89 kV/cm) at MPB compared to all other compositions. The electromechanical planar coupling coefficient (kp) was measured through the resonance and anti-resonance method using the LCR meter. The piezoelectric strain coefficient (d33) measured directly using the d33-meter. At x = 0.5 composition the highest value of d33 = 398 pC/N is obtained.

Jan 1, 2012

By Kathryn C. Sole

A novel solvent-extraction process for the refining of gold was recently commercialised, with the commissioning in May 1997 of a 24 t a-' refinery at Harmony Gold Mine in Virginia, South Africa. The MinataurTM Process (Mintek Alternative Technology for Au Refining) uses solvent-extraction technology to produce gold of 99.99% purity from the cathode sludge arising from a conventional carbon-in-pulp / electrowinning circuit. Implementation of this process introduces significant cost benefits compared with the conventional dore smelting / toll-refining route previously followed. This paper outlines the process, presents selected operating results obtained during the first few months of operation, and provides some details of the associated techno-economic advantages.

Jan 1, 1998

By Peng Bing

Stainless steelmaking dust is classified as a hazardous waste due to higher than acceptable heavy metal leachabilities such as zinc, lead, cadmium and chromium. In addition to being an environmental hazard, the flue dust is also an economical concern to stainless steelmakers as it contains large amounts of valuable alloying elements, especially for iron, chromium and nickel. A new technology of direct recycling of stainless steelmaking dust has been developed to recover the metals from the dust. But it was found that zinc was accumulated in the dust collection system in practical run of direct recycling. This study focuses on the effect of the operating parameters such as temperature, dust feed rate and the ratio of CO to dust on the reduction of zinc oxides present in the dust. The mathematical model for the reduction process was setup based on the experimental research. According to the mathematical model, the temperature has obvious effect on the reduction of zinc. It is benefit to the process of zinc reduction to increase the temperature. But the temperature will not be the main factor for the reduction process after 1228C. It will promote zinc reduction to decrease the dust feed rate and control the ratio of dust to CO. It was also found from the experiments that ZnFe2O4 in the dust could be decomposed at high temperature. Decomposing ZnFe2O4 in the dust increases the recovery of zinc from the dust distinctly.

Jan 1, 2006

By Laurentiu Nastac

"Two advanced control solidification technologies were studied in this article to improve the quality of the cast ingots as well as to control the solidification structure evolution during the plasma arc melting (PAM) processing of Ti-6-4 ingots: (i) electromagnetic stirring (EMS), and (ii) ultrasonic treatment (UST). The developed EMS modeling approach is based on the numerical solution of Maxwell's equations, fluid flow, and heat transfer equations, and mesoscopic modeling of the grain structure. The UST analysis tool is capable to model acoustic streaming and cavitation. It is used in this work to study ingot solidification under the presence of ultrasound. Predictions of the macrostructure, GET formation and primary dendrite arm spacing for PAM Ti-6-4 ingots processed with and without EMS or UST were discussed.1. IntroductionTitanium (Ti) alloys are melted, refined and cast into ingots through plasma arc cold hearth melting (PAM), electron beam cold hearth melting (EBM) and vacuum arc remelting (VAR) for jet engine applications. Process modeling has become a viable tool to optimize the PAM, EBM, and VAR processes. A comprehensive modeling approach to simulate ingot solidification phenomena in primary melting and secondary remelting processes of Ti alloys would include models for macroscopic mass transfer, heat transfer, fluid flow, acoustic, electromagnetic and species transport. The approach should also include microscopic models to predict the evolution of grain structure in solidifying ingots in conjunction with electromagnetic stirring (EMS) and ultrasonic stirring (UST)."

Jan 1, 2012

By Edgar Peek

Lixiviant regeneration is by definition a precondition for any hydrometallurgical process. In chloride hydrometallurgy either HCl or Cl2 has to be regenerated in order to establish an economically viable metallurgical process. One such regeneration process is widely used with steel pickling where HC1 is regenerated through the thermal decomposition of ferrous chloride in either spray roasters or fluid bed pyrohydrolyzers. This standard HC1 regeneration process deserves to be considered as a potential separation process, since thermodynamic calculations show that a fluid bed pyrohydrolyzer can function as a ferrous-nonferrous separator. Several nonferrous,metals such as zinc, lead and cadmium can be volatilized as a chloride under ferrous chloride pyrohydrolysis conditions. If such a nonferrous metal volatilization could be achieved in the case of slurry feeding of "contaminated" iron oxides, then this would increase the Fe/H2O ratio of the (process) feed and thus save on fuel per ton of iron, while yielding a marketable iron oxide product. Previous test work on synthetic materials revealed that the near-complete separation of zinc, lead and cadmium from iron oxide was possible in a pyrohydrolytic atmosphere, even if zinc was present as zinc ferrite (more than 99.5%). This investigation, which was carried out in a tube furnace at 1100 K has now been extended to treat synthetic zinc minerals and also franklinite ore. For the latter, it was found that 85% zinc volatilization could be achieved in 4 hours at 1300 K. It is postulated that complete zinc volatilization could not be attained due to the formation and/or presence of gahnite and hardystonite, which might be stable in HCl/H2O atmospheres at 1100 K. The effect of adding small amounts of calcium chloride to react with gahnite and hardystonite to give zinc chloride and both calcium aluminates and silicates is being discussed. Test work on slurry feeding of this complex ore in a recently constructed 4-inch diameter fluid bed pilot unit has been planned for the near future.

Jan 1, 1995

By Kazusuke Sato, Takahiro Uno, Koji Hoshino

"A novel Ni coating technique of Ni(OH)2 powders was developed to improve the positive-electrode performance· of the Ni-MH batteries. It was found out that Ni(OH)2 powder was reduced by N2H4 without any catalysts in an alkaline - solution at high temperatures. In result of observation of pH and potential changes in the solution during the reaction, it was found that the reduced species was HNio2- ion dissociated from Ni(OH)2 in the alkaline solution. The molar fraction of reduced Ni of the Ni(OH)2 was increased in proportion to the amount of added N2H4. At the small Ni fraction, a porous Ni layer was formed on the surface of Ni(OH)2 powder. Open cell tests were carried out with the paste type electrodes made of either the Ni coated Ni(OH)2 powder or non-coat powder, and cell performances were compared. In result, it was found that the Ni coating technique is effective on improvement in the utilization of Ni(OH); as a positive-electrode active material under high current densities.IntroductionNi-MH rechargeable battery is generally used for the power source of portable machines and electric vehicles because of its good performance at high energy density and. long term cyclical life as well as cleanness and good safety. Cell component materials have been improved respectively, and as concerns ·the positive-electrode reducing 'the internal resistance is a principal problem to improve the discharging performance at higher current densities.In recent years, improved Ni(OH)2 powders coated with conductive materials as NI. or CoOOH have been developed for the· positive-electrode active materials in order to· reduce the internal resistance of the electrode1)· 2) The Ni coated Ni(OH)2, however, is costly because it is fabricated by .the -non-electrode plate technique which needs a expensive precious ·metal catalyst as PdC12We found that Ni(OH)2 powder was reduced by N2H4 without any cryatalysts in an alkaline solution at high temperatures. After the treatment, Ni(OH)2 powder become gray color like Ni powder from light-green color; and. turned into a magnetic. In this study, the mechanism of the -reducing reaction was investigated to apply the reactions .to a novel Ni coating technique of Ni(OH)2 powders, · and the performance of the Ni coated Ni(OH)2 powder obtained by the reducing process was evaluated as an -positive-electrode active material of Ni-MH batteries."

Jan 1, 2000