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By Ma Keyi, Yang Xianwan, Zhu Xiaoyun, Guo Zhongcheng, Zheng Yanping

"The oxidation of the Multifunctional Electrodeposited RE-Ni-WP- SiC Composites at high temperature is investigated. The results show that during high temperature oxidation the relationship between the mass change of pure Ni , Ni-W-P, Ni-W-P-SiC or RE-Ni-W-P-SiC coating and the oxidation time follows a mixed curve, i.e. it is approximately a linear relationship when the oxidation time is less than 60 mins while it is a power function relationship when the oxidation time is over 60 mins. The order for the oxidation rate of the four coatings is Ni> Ni-W-P> Ni-WP- SiC>RE-Ni-W-P-SiC. The mass change of Ni-W-P, Ni-W-PSiC or RE-Ni-W-P-SiC coating increases exponentially with a rise of oxidation temperature. The high temperature-oxidation resistance of RE-Ni-W-P-SiC composite coating is 3-4 times that ofNi-W-P alloy coating. The cross section morphologies and Xray diffraction patterns indicate that the high temperature oxidation resistance of RE-Ni-W-P-SiC composite coating is better than any other coatings.1. IntroductionWith the rapid development of modem industries the products in engineering industry are continually challenged by the requirements of long-term and stable working at higher temperature, pressure, speed and under adverse conditions. Consequently, the surface properties of the products, such as the resistance to oxidation at high temperature, the resistance to wear and the resistance to corrosion, should be improved continually."

Jan 1, 2000

By T. Tamagawa

Vaporization of zinc and mixing of zinc vapor with CO-CO2 mixtures were studied experimentally to prepare Zn(g)-CO-CO2-Ar mixtures with desired composition for investigating the condensation behavior and efficiency of zinc vapor. The vaporization rate of zinc was generally constant under given conditions, and could be increased by raising the flow rate of the carrier gas, temperature and vaporization area. The Zn(g)-CO-CO,,-Ar mixtures were quenched by a water-cooling sampling tube for measuring the actual composition of the mixtures in the reactor. The oxidation extent of the zinc vapor in the CO-CO2 mixtures had relation to the CO2/CO ratios and the temperatures. Under current conditions, it was necessary to employ the CO2/CO ratio below 0.125 for mixing the zinc vapor with CO-CO2 mixtures without oxidation. In addition, the appearances and zinc contents of the condensed zinc on the sampling tube were also examined.

Jan 1, 2001

By Henrik Gudbrandsen, Geir Martin Haarberg, Ana Maria Martinez, Karen S. Osen, Sverre Rolseth

"The Several approaches were tried for developing an electrochemical route for producing high purity silicon from molten salts. K2SiF6 and metallurgical grade silicon were used as the source of silicon. Molten LiF-KF and pure KF with additions of K2SiF6 were used as electrolytes at temperatures from 550 - 900 oC. Silicon was cathodically deposited and anodically dissolved in the fluoride electrolytes. High electrorefining efficiency was obtained for many elements after electrolysis experiments at constant potential or constant current. The main challenge was to reduce the contents of boron and phosphorus. Another difficulty was to remove inclusions of solidified electrolyte. The lowest energy consumption was estimated to be ~ 3 kWh/kg Si, while the best current efficiency for Si deposition was found to be ~ 95 %.IntroductionSilicon is the most important material for photovoltaic power generation devices because of high feasible efficiency, low ecological impact and slow degradation. Development of a new and less expensive route for producing silicon of the desired quality is necessary in order to make solar cells competitive. Electrochemical routes may be an alternative possibility, and many laboratory studies have been reported over the past few decades. Most of the studies have been performed in molten salts, chloride or fluoride, at moderate temperatures so that solid silicon was deposited at the cathode. The production of high purity silicon has shown an annual increase of about 25 %, due to the increasing demand of solar grade silicon (SoG-Si). For future increased use of solar energy it is important to develop alternative, more energy efficient and cheaper processes for SoG-Si production compared to the Siemens process.Common silicon sources have been SiO2 and K2SiF6 for electrowinning and MG-Si in the case of electrorefining. A serious challenge is to find an oxygen evolving anode for electrolytes containing dissolved oxides. Especially at moderate to high temperatures and in molten fluoride electrolytes this is a difficult task.Many experimental results have been reported in molten chloride electrolytes. Nohira et al. [1-3] and Chen et al. [4] cathodically deposited silicon by electrodeoxidation of solid SiO2 in molten CaCl2 by potentiostatic electrolysis. An alternatice approach is to use electrorefining of low-cost metallurgical grade silicon (MGSi) to produce SOG-Si. In previous studies [5], an MG-Si anode was used, and silicon was successfully electrodeposited on a molybdenum wire in a CaCl2 based melt. It was found that the anode was strongly passivated due to the precipitation of silicon. Also, some deposits detached from the molybdenum wire because of the poor adherence to the cathode.Considering the Cu-Si alloy which has a good segregation effect for some impurities, and should not passivate, could be a good candidate anode for electrorefining. [6]."

Jan 1, 2014

By X. J. Wu

Effects of various factors such as diaphragm materials, composition of electrolytes and current density on copper electrowinning from cupric chloride solutions was investigated. It is found that the crux of this process is to prevent the dissolution of copper by cupric ion and the formation of suspended CuCl precipitate. A process with high difference of copper concentrations between the feed solution and the spent electrolyte was selected. With this process, in which the feed solution contains 90 g/dm3 [Cu"], 3M NaC1, and 10mg/dm3 bone glue, and the spent electrolytes contains 10 g/dm3 [Cul, a very smooth and dense copper cathode can be produced with current efficiency above 93% and energy requirement less than 1.7 kwh/kg Cu at 25°C with N2 sparging. If a slightly higher energy requirement is permitted, smooth and dense copper cathodes can be produced at the current density up to 800 A/m2 with the identical solutions.

Jan 1, 1991

By R. H. Hanewald

INMETCO, a subsidiary of Inco Limited, is the only facility in North America that provides High Temperature Metals Recovery for nickel-, chromium-, and iron-bearing wastes. Since 1978, this process has prevented more than 775,000 tons of materials from becoming part of the nation's waste stream. The paper describes Inco's experience in metals recovery, traces the development and explains the operation of the High Temperature Metals Recovery Process, and examines the procedures and criteria used to determine whether spent catalysts meet process feed specifications. An overview of the current requirements for transporting spent catalysts is provided. The paper concludes with brief case histories of catalysts users employing High Temperature Recovery to manage spent catalyst.

Jan 1, 1995

By Ali Akbar Mottahedi

Chromate conversion coating is a process for making a complex layer at the surface of zinc galvanized steel which makes the metal more resistant to corrosion, especially at marine atmosphere, and increases the adhesiveness of color. In this work the influences of various compositions on commercial zinc galvanized steel sheet to the color of chromate conversion coating has been investigated at normal temperature and the factors that affect the control and optimization of the process have been determined. A bath composition of 20 g/liter Cr203 and 10 g/liter NaOH and a dipping time of 50 seconds at room temperature (25-30°C) make a desirable color of chromate coating. A slow agitation at a constant pH of I (with additions of NaOH or H2SO4) assures a constant bath condition and develops the color. This kind of coating has more corrosion resistance and this bath condition and composition are also more economical.

Jan 1, 2003

By P. S. Arthur

The ISASMELT? process is a submerged lance smelting technology operating in smelters in Australia, the USA, Belgium, India, Germany, Malaysia and China. Further plants are under construction in Peru and Zambia. Following the invention of the Sirosmelt lance technology Mount Isa Mines recognised the commercial potential in the novel top blown bath smelting process and embarked on a development program that has lasted more than 25 years. After successful operation of pilot plants and demonstration plants producing copper and lead, Mount Isa Mines decided to license the technology to external companies. Since the purchase of Mount Isa Mines by Xstrata in 2003, Xstrata Technology has assumed responsibility for transferring the technology to ISASMELT? licensees. In the 15 years since the first commercial furnaces started operation plants have been constructed (or are under construction) with a combined annual smelting capacity of more than six million tonnes of concentrates or secondary raw materials. Process development continues on the commercial scale plants at Mount Isa and elsewhere. Many of the improvements implemented by plant operators have been passed on to, and adopted by, other licensees. Exchange of ideas and technical improvements occurs through ad hoc visits to fellow licensee sites and through regular licensee workshops arranged by Xstrata Technology. This paper updates the reader on the status of various ISASMELT? plants either operating or under construction. It highlights the important role that the technology provider?s operational experience plays in ensuring that new smelting plants ramp up quickly to nameplate capacity.

Jan 1, 2006

By Jeffrey L. Zelms

Environmental issues and how they are addressed -- or not addressed -- by the lead industry in the 1990s will determine the eventual fate of lead mining in both the U.S. and worldwide. Clearly, governmental regulation throughout the West will become harsher. Equally clearly, the industry has? failed to educate the public regarding lead. Instead of public support for a critical mineral, we face widespread public ignorance and paranoia. If we can demonstrate the public interest benefits of the industry, the 1990s will be a decade of continuing growth -- not dynamic growth, certainly, but growth at least comparable to the world economy. If, however, we fail to demonstrate the industry's public interest benefits, the 1990s could mark the beginning of the end of our business.

Jan 1, 1990

By S. C. Dhara

The recovery of Platinum Group Elements from various industrial scraps and spent materials in the form of high and low grade, such as, impure metals, matte, catalysts and other ceramic substrates, etc., has .been described by using high pressure reaction method. Nickel, Stainless Steel, Titanium and glass lined reaction vessels? are used in the reaction process. Primarily, the method involves either direct leaching of the substrates from the metal value or dissolving the precious metal from the substrate. Both acids and alkalies are used along with other reagents in the reaction process. The temperature and pressure of the leaching process are the main criteria for the reaction kinetics.

Jan 1, 1989

By Hal dun Kurama

In thus-study, Bigadic upper zone zeolitic tuff, which contains about 87% clinoptilolite was used as an ion exchanger for removal of Pb++, Cu++, Cd++ and Hg++ ions from wastewater. Bench scale experiments with two different glass columns, were carried out continuously under the closed/ open circuit conditions. Before ion exchange tests, zeolite samples were treated with NaCI (6ml/ min. and 42BV). The effects of particle size, bed volume, pH and flow rate on the ion exchange capacity were determined. Under the best operation conditions, the effect of initial influent solution concentration on ion exchange selectivity was tested. As a-result, it was found that the Bigadiç clinoptilolite had the following ion exchange capacities;

Jan 1, 1995

By Y. H. Wang, S. Kou

"Three-dimensional weld pool convection was computer simulated using dimensionless variables. The electromagnetic force, the buoyancy force and the surface tension gradient on the pool surface were treated through the use of the dimensionless electromagnetic force, the Grashof number and the Marangoni number. Other typical dimensionless numbers such as the Prandtl number and the Peclet number were also used. The calculated and experimentally observed fusion boundaries were compared. The convection patterns were shown and the effect of the Marangoni number was demonstrated. IntroductionSeveral weld pool convection models have been developed by Oreper et al. (1,2), Chan et al. (3) and Kou et al. (4). These models describe two dimensional convection in stationary weld pools in a semi-infinite workpiece. Since the vast majority of arc welding practices involve a moving heat source and weld pool, and the workpieces are finite in thickness rather than semi -infinite, a 3-D convection model for a moving heat source and a workpiece of finite thickness is expected to be much more useful.Weld pool convection can strongly affect the structure and properties of the resultant welds. Variations in weld characteristics which are likely to occur from changes in weld pool convection are: weld penetration, macrosegregation, gas porosity, solidification structure, undercutting and surface smoothness. Apparently, the quantitative understanding of convection and heat flow in weld pools is of considerable practical interest. Mathematical models describing convection and heat flow in weld pools are essential, not only because of the quantitative understanding they provide, but also because of the difficulties associated with the experimental measurements of weld pool convection. These difficulties are mainly due to the fact that only surface flow, rather than the overall convection pattern in the weld pool, can be observed. In fact, due to arc glow even the observation of surface flow can be rather inconvenient."

Jan 1, 1986

By Veneta Groudeva

A pyritic ore containing zinc, lead and copper as? the relevant primary sulfide minerals, .as well as gold and silver finely disseminated in the sulfide matrix, was? leached in percolation columns. Each column contained 30 kg of ore crushed to minus 10 mm. Firstly, zinc and copper were efficiently leached by means of chemolithothrophic bacteria? in acidic sulfate bearing medium. Zinc was leached more rapidly than copper but the final extractions of these metals were similar (about 75% in 300 days). A part of the galena was oxidized to the. insoluble lead sulfate during the leaching. The pyr:ite was, however, relatively slightly attacked. The ore was then leached by means of FeC11 - HCl solutions both in the presence and in the absence of bacteria to solubilize the lead. The chemolithotrophic bacteria grew in media containing both chloride and sulfat~ ions and maintained a high ferric to ferrous ion ratio in the percoiating solutions. The chemical leaching was, however, more efficient since ft was possible to carry it out at higher chloride ion concentrations. About 10% of the lead was leached in this way in 90 days. Finally, the ore was leached by thiourea in the presence of a gold-oxidant (oxone) to extract the gold and silver. Over 60% of the gold and over 55% of the silver were extracted from the ore in 150 days, while. the extractions of these precious metals from an untreated ore sample were lower than 25%.

Jan 1, 1991

By J. E. Wey

Extraction of cobalt from cobalt sulfide and cobaltite flotation concentrate from the Blackbird Mine, Idaho, was investigated using an adapted strain of Thiobacillus ferrooxidans. Cobalt extractions as high as 100% were realized in the inoculated experiments, whereas only 4% extraction was obtained in the sterile run. The influence of pulp density on the rate and extent of cobalt extraction was also determined. It was found that the extraction of cobalt followed predominantly the indirect mode of bacterial activity. In this process, ferric iron oxidizes cobaltite to cobalt sulfate and ferric arsenate while being reduced to its ferrous state; the bacteria continuously re-oxidize ferrous to ferric iron. Electrochemical measurements using cyclic voltammetry suggested that cobaltite oxidation involved a number of intermediate reactions.

Jan 1, 1993

By Liu Zhonghua

Hydrogen reduction of cobalt sulfide (Co9S8) was experimentally investigated in the temperature range 813-1053 K. The results revealed that the reaction kinetics can be described by the shrinking core mod¬el in chemical control regime at low temperatures, it is of first order with respect to hydrogen concentration, and the reaction activation energy is 67.4 kJ/mol. The SEM second electron images of the samples before and after experiments showed that the swelling of the sample above 973 K is due to the formation of metallic cobalt whiskers.

Jan 1, 1992

By Jie Li, Thomas A. Rawdanowicz, W. J. Collis, S. Venkatraman, S. Iyer

"InSb being the lowest band gap. material amongst the 111-V semiconductors with low effective mass has long attracted research interest, due to its potential application in far infrared devices and for high speed circuit elements. In this paper, we report, for the first time, Te-doping of InSb on GaAs substrate using SnTe doping source with molecular beam epitaxy (MBE) technique and its electrical characterization. The undoped epilayers are n-type in the temperature range of 10 K to 300 K investigated. The room temperature (RT) mobility as high as 64,810 cm2/V·s (1.9x1016 cm-3) have been measured on a 4.8 µm thick epilayer. Sn Te doping at different doping levels were investigated. 5. 7 µm thick doped layers with RT carrier concentrations ranging from 2x1016 cm-3 to 3.2x1018 cm-3 with corresponding full width at half maximum (FWHM) of x-ray (400) rocking curve varying from 170-200 arc-seconds have been achieved. The Hall mobility of 20,000 cm2/V·s at 1.3xl018 cm-3 carrier concentration was obtained indicating that SnTe is a good candidate as source material for n-type doping of InSb.IntroductionThe thin films of InSb and InSb-based alloys have found considerable interest because of potential applications in III-V semiconductor-based infrared optoelectronic devices1• In addition, the advantage of the small effective mass and the consequent high mobility can be utilized in high frequency and high-speed circuit devices2 InSb can also be used in magnetoresistive sensors for position sensing3. Epitaxial InSb films grown by MBE may be doped n-type with Si or Sn, or with the group VI elements, namely, S, Se, or Te. Of the group VI elements, Te may be advantageous because of its relatively low vapor pressure. However, the vapor pressure is high enough to have sufficient memory effect during MBE growth. Hence different telluride compounds such as GaTe45, PbTe6 and Sb2Te37 have been used as the dopant source for Sb-based compounds. SnTe has also been used as a successful n-type dopant in the MBE growth ofGaSb8 But, to our knowledge, there is no report on the investigation of SnTe doping of InSb. In this paper, we report the first doping characteristics of SnTe in InSb layers grown on GaAs substrate."

Jan 1, 1998

By Takamitsu Nakasuga, Haiping Sun, Kyushu University, Katsumi Mori

"The kinetic behavior of reduction of chromite ore by liquid iron containing carbon and silicon has been investigated under various experimental conditions to clarify the reduction mechanism. It was found that the reduction rate of chromium ore by liquid Fe-C alloy was very slow. In addition, when carbon and silicon coexisted in the iron melt, silicon was found to preferentially oxidized to form silica, which favored for the fonnation of liquid slag and the rate of reduction was considerably accelerated. The similar effect was obtained by the addition of some fluxes, such as SiO2, Na2B407, CaO-SiO2, which also promoted the formation of a liquid slag and thus the reduction rate in the early stage also increased.IntroductionThe reduction of Cr2O3 is a basic reaction for production of ferro-chromium from chromite ore and for chromium recovery from the slag fonned during the decarburization period of a stainless steel-making process. The reduction of chromite ore consumes much energy and its reaction rate is not so high. Thus, in order to increase the reduction efficiency, it is strongly desired to clarify its reduction mechanism from the practical and the theoretical points of view."

Jan 1, 2000

By Carla Lupi

In this work, nickel-cobalt electrodeposition under galvanostatic conditions was investigated. Ni-Co alloy was electrowon from an acid sulphate bath containing 40 g/L Ni and2-8 g/L Co.. The effect of electrolyte composition, current density, temperature, solution pH and presence of buffers such as H3BO3 and (NH4)2SO4 on Co content of the binary alloy has been investigated. In particular, current densities ranging from 180 to 400 A/m2 and temperatures ranging from 27 to 60°C were tested. The composition of Ni-Co alloys may be diversified through the selection of process parameters. The experiments show that the highest cobalt content of the alloy is reached by using a buffer free electrolyte without solution pH control. Though, in these conditions, the most homogeneous, fine and regular deposit morphology is obtained, energy requirements are the highest in tests lasting just two hours.

Jan 1, 2003

By Pekka Parvinen, Saija Luukkanen, Pentti Pirkonen, Väinö Hintikka, Hannu Sekki

In the study was developed a new method for the treatment soils contaminated by polychlorinated dibenzodioxin and dibenzofuran. The method is based on attrition of soil so that the contaminants absorbed on the particle surfaces are liberated with the fine fraction formed in the attrition process. Same the attrition process produces active surface which can absorb the free contaminants. Before starting the remediation process must be decided the limit value under which the residual concentration must lie. Then in the laboratory is performed an experiment in the base of which is determined the grain size level; material under which much be removed together with the contaminant. In the real sample has been found that after the attrition the limit value 0.5 ng/g (I-TEQ) is obtained when the fine under 0.1mm fraction (20% of the original soils amount) is removed together with the contaminants 96% (original level 10 ng/g; 100%).

Jan 1, 2008

By V. Ramachandran

Under the Resource Conservation and Recovery ACT (RCRA), generators of listed or characteristic hazardous wastes must find satisfactory means for disposal. of wastes. Initially, for many this meant landfills and deep-well injection. Until recently, mining and metallurgical by-products have largely been exempt from RCRA, but now are coming under its jurisdiction. With the increasing closures of landfills, companies in the U.S. such as electroplaters, miners, metallurgical plants and others are turning to recycling as an alternative to treat their wastes. While the cost of recycling has been challenging, the long-term economics prove attractive because recycling interrupts the cradle- to-grave responsibility for the waste generator. The present paper describes the recycling of hazardous wastes at ENCYCLE/TEXAS. Encycle extracts marketable metals from metal-bearing sludges and wastewater using hydrometallurgical processes borrowed from the mining and metallurgical industry.

Jan 1, 1994

By John W. Lund

The Geo-Heat Center has been investigating the utilization of waste silica from the Cerro Prieto geothermal field for several years. The main objectives of the research were to com-bine silica with various additives to (1) form bricks for low cost housing, and (2) to produce a suitable road surfacing material. The various additives that were tested included hydrated lime, portland cement, plastic fibers, asphalt cement and emulsified asphalt. The silica-cement combination produced the strongest bricks and had the best weather resistance, whereas, the silica-lime combination produced the bricks with the lowest thermal conductivity and specific gravity density. The addition of plastic fibers to the silica-lime mixture improved both strength and weather resistance. The combination of asphalt and silica is not suitable as a road surfacing material, however, silica-cement appears promising.

Jan 1, 2006