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By G. A. Brooks

Increasing interfacial area through gas injection is one of the main methods for accelerating reaction between slag, metals, and gases in modern pyrometallurgical reactors. In slag-metal reactors, the generation of a large number of metal droplets into the slag phase through high gas velocity has a much larger effect on the overall kinetics compared to the enhanced mass transfer through mixing. Top blowing technology generates large interfacial areas (>300 m2/tonne) through high impingement gas velocity at short distances between the exit of the injection lance and the metal-slag interface. Phase separation may become a limit at the case of very high interfacial areas, though there is still only limited understanding of the trajectories of metal droplets in slag-metal-gas emulsions.

Jan 1, 2003

By Lifeng Zhang, Zineb Benouahmane, Yaqiong Li

Experimental oxidation tests at high temperature (1000-1200 °C) on SiC samples have been respectively performed under wet and dry air atmosphere for different holding times. The thickness of thermally grown oxide was experimentally measured by DEKTAK Stylus Profilometry. The results showed that the oxidation rate was increased with temperature and holding time, corresponding to a passive oxidation regime which led to the formation of SiO2 layer. The sessile drop method was employed in order to measure the contact angles between Si and SiC at high temperature. Contact angle can be varied from 39.6° to 75.6° by controlling the atmosphere. The deoxidation of the oxide layer and infiltration of liquid silicon caused a decrease in the contact angle.

Jan 1, 2016

By Jinrong Zhang

Fresh cyanide solution was treated by near UV light with the assistance of photocatalysts. Cyanide was oxidized mainly to cyanate. Photochemical behavior of the anatase and rutile forms of TiO2 was compared. It is found that anatase has a much higher activity than that of rutile. Bubbling of oxygen in the reactor showed no appreciable increase in cyanide oxidation, implying that the reaction is surface controlling. A very interesting finding in this study is that a natural mineral, ilmenite, can replace chemical titanium dioxide as the photocatalyst. Ilmenite without any treatment did not catalyze the oxidation of cyanide. But, after being roasted at high temperature with oxygen, the oxidation was enhanced dramatically. The mechanisms of photooxidation of cyanide and the roasting of ilmenite are proposed.

Jan 1, 1991

By Milan Lj. Stamatovic

The hydrometallurgical recovery of zinc from recycled blast furnace dust from a steel plant (Smederevo Metallurgical Company - Yugoslavia) was investigated. The dust contained 22% Fe, 17% Zn and 0.2% Pb. X-ray diffractometry showed that the main components were hematite and magnetite, in combination with zinc oxide and a very low content of lead oxide. Individual particles were generally spherical and ranged in size from 10 to 150 microns; 63% were less than 33 microns in diameter. An effective hydrometallurgical approach proved to be by caustic leaching followed by electrowinning. Recovery of zinc in the form of zinc powder was over 90%. This powder can be used for the cementation of impurities in the conventional hydrometallurgical process for zinc production.

Jan 1, 1993

By Kazuya Koyama

The leaching of copper from a printed circuit board (PCB) and the electrodeposition of copper from a cuprous solution in ammoniacal alkaline solutions were examined in order to develop an energy-saving hydrometallurgical process for copper recovery from electronic scrap. In the leaching experiments, copper in the PCB was oxidized by Cu(II), and Cu(I)-ammine complex ions were formed. The copper(I)-ammine complex slightly depressed the leaching rate, while Cu(II)?ammine markedly enhanced it. During the electrodeposition experiments, the current efficiency of copper deposition was approximately 100% in the current density range of 200 to 1000 Am-2. The electrodeposition of copper from the Cu(I)-ammine complex solution favored the production of plates rather than powders.

Jan 1, 2003

By W. Petruk

The silver-rich cobalt-nickel arsenides ores of the Cobalt area in Ontario, Canada were mined for silver from about 1904 to 1985. The ores contained about 8 oz to 100 oz Aglt and about 1 wt% Ni and 2 wt% Co. They were processed by gravitational techniques, screening and flotation to produce separate silver and Fe-Co-Ni arsenide concentrates. The silver concentrate was smelted, and in some cases the arsenide concentrate was sold to custom smelters which recovered silver and other metals. The ores display a wide variety of textures and contain many minor and trace elements. This paper presents an evaluation of mineral characteristics that have a bearing on extractive metallurgy and smelting of this type of ore.

Jan 1, 1993

By C. A. Landolt

Inco pioneered the use of tonnage oxygen in non ferrous metallurgy when it commissioned the first industrial oxygen f1ash smelting process for the treatment of copper concentrates in the ear 1y fifties. This techno logica1 innovation was followed by other applications of technical oxygen. Inco is currently implementjng a Sulfur Dioxide Abatement Program designed to reduce SO2 emissions from the smelter by 60% in 1994. The new flowsheet includes new equipment for the oxygen flash smelting of Cu-Ni concentrates and for flash conversion of chalcocite. Oxygen smelting and converting technology will lead to a substantial decrease in use of fossil fuels and to generation of high strength S02 off gases suitable for efficient fixation in a new acid plant.

Jan 1, 1992

By Zenjiro Asaki

The copper concentrate particles dissolve quickly into the molten matte in the smelting furnace of Mitsubishi Process, which indicates that the sulfide smelting is essentially a gas/liquid reaction. In this paper, theoretical calculation has been made on the rate of oxidation of FeS component in the matte to form FeO by rising gas bubbles using the penetration theory. The results showed that all the oxygen in the bubble of 1.2 cm in diameter, which is the maximum stable diameter, is consumed in 3 ms. This time required is sufficiently short, and it results in the actual operation of smelting furnace of 1100% oxygen-efficiency. These calculations indicate that most smelting reactions are completed just under the lance, except slag formation.

Jan 1, 2002

By Kazuya Kitatani, Gen Sasaki, Naoto Ohta, Hideharu Fukunaga, Makoto Yoshida, Jin Pan, Kenya Nagahisa, Toshihiro Ishikawa

"A sintered SiC (Tyranno-SA) fiber-reinforced MAS glass matrix composite was fabricated by using a slurry infiltration method and hot-pressing. The microstructure and mechanical properties were investigated: To prepare the preform, the MAS glass slurry including a dispersing agent was infiltrated into a bundle of the fibers. The preform was then hot-pressed under the conditions of 1473 K, 30 MPa, 3.6 ksec. A unidirectionally-reinforced oxide matrix composite with 50% Vf. of the fiber and a density of 2.84 g/cm3 was obtained. As the mechanical properties at room temperature, the three-point flexural strength- and quasi-static adsorbed energy were 500 MPa arid 6,000 J/m2, respectively. Without graphite or an h-BN pre-coating on the surface of the fiber, pull-out and bridging of the fibers from the matrix was found, and this leads to a high value of the adsorbed energy. By TEM observation, nano-scale crystalline products were found between the fibers and the glass matrix. The push-out test reveals that this layer causes the appropriate debonding of the interface during the fracture process of the composite.Introduction It is known that the CFCCs (continuous-fiber-reinforced ceramic matrix composites) are characterized by their non-linear fracture behavior, which is' hardly found in monolithic ceramic materials. It is inevitable for the CFCCs to exhibit a large fracture toughness so 'that debonding of the fiber/matrix interface; pull-out and bridging of the fibers then' occurs during the fracture process. This series of fracture behavior is known as the so-called ""the mechanism of toughening of the CFCCs"". Thus, different from the MMCs in which strong interfacial bonding is necessary, the interfacial strength of the CFCCs has to be controlled. As techniques for controlling the interfacial strength, it is also known that both a CVD-graphite coating and an h-BN coating are effective to induce the mechanism of toughening[1,2]. In the case, of the Si-C-O or Si-Ti-C-O fibers/glass or crystalline oxide matrix composites, it is reported that the formation of the in-situ graphite layer, which is also effective to increase the fracture toughness of the CFCCs, is often found during the fabrication process such as hot-pressing. The lower the crystallinity of the Si-C-O fibers, the higher is the tendency to form the in-situ graphite layer as found by the chemical reaction between the fibers and the glass matrices[3-12]. On the-other hand crystallized stoichiometric 'SiC fibers are attractive for high temperature service because of the higher phase stability compared to the Si¬C-O or Si-Ti-C-O fibers. However, in the previous, studies, the mechanical properties and the interfacial chemical reaction of the crystallized SiC fibers / glass matrix Composites have still been unknown. In this study, a polycrystalline 'sintered SiC fiber-reinforced MAS glass composite was fabricated. The mechanical properties and microstructure were then investigated. The slurry infiltration technique followed by hot-pressing was used to prepare the composites. The formation of the in-situ graphite layer and the relationship between microstructure and mechanical properties at room temperature were examined by the TEM observation of the fiber/matrix interface."

Jan 1, 2000

By Aureo D. V. Machado

An experimental study to obtain zirconia powders (ZrOz) from carboxylate zirconium solutions followed by hydrogen peroxide stripping and precipitation, has been carried out. Zirconium carboxylate was prepared by solvent extraction from a chloride aqueous phase using magnesium carboxylate as organic phase. The variables examined in the precipitation reaction were: Temperature: 25 - 90 ?C ? H202= concentration: 0.3 - 5% wt/wt - pH: 1 ? 9 Organic/Aqueous ratio (1/1) and reaction time (30 minutes) were maintained at constant levels. The optimum results (98% precipitation) were achieved at 25 °C, 5 % wt/wt H202=, and pH = 5. The precipitates were composed of large amorphous aggregates (<I00 micrometers). After calcination for 1 hour at 1000 OC, monoclinic ZrO2 with a large variation in particle size (1 -100 micrometers) was obtained.

Jan 1, 1991

By John J. Mahoney, George P. Demopoulos, Matthew T. Bohan

In recent times processing of arsenic-laden complex ores and heightened awareness of the detrimental health effects of arsenic has put an increasing burden on metallurgical operations to remove arsenic from processes for disposal in an environmentally stable form. At present, arsenic is removed and prepared for storage by precipitation of insoluble secondary arsenic-bearing minerals. It has been suggested that Ca(II)-Fe(III)-As(V) phases resembling the natural mineral yukonite, under certain conditions, may have a role in controlling arsenic pore water concentrations in arsenical waste storage facilities. In this study, a previous synthesis method of yukonite (Ca3Fe5(AsO4)4(OH)9⋅4H2O) is revisited and new solubility/stability data is presented based on a modified method.

Jan 1, 2014

By J. M. Tourre

Recently, interest in rare earth based oxide powders for electronic applications has risen dramatically. Considerable research has been devoted to the chemical synthesis of these compounds to improve the control of physical and chemical characteristics of the powder. In most cases, a high degree of homogeneity, purity and reproducibility is necessary in order to obtain good application properties. The synthesis parameters can control particle size, surface area, and morphology as well as the degree of homogeneity and application properties. Rhone-Poulenc, a world leader in the production of separated Rare Earth chemicals has developed a flexible process to produce a wide variety of compounds. The different processes for the synthesis of YBa 2Cu 3 O 7 will be discussed and compared to the RP process in term of product quality, cost and flexibility.

Jan 1, 1992

By Ravinder N. Reddy

Electrochemical capacitors are charge storage devices. They bridge the gap between dielectric capacitors and batteries in terms of energy and power density. Electrochemical capacitors are classified into two types, electrochemical double layer capacitors (EDLCs) and capacitors based on pseudocapacitance. In EDLC, charge is stored at the interface between electrode and electrolyte. Carbon is considered to be prime electrode material for EDLCs due to its many favorable characteristics. In this study carbon materials are derived from thermal decomposition of catechol- formaldehyde polymers and are studied as electrode material for electrochemical double layer capacitors. Carbon electrode surface is characterized using NOVA 1200 gas sorption analyzer. It is also characterized using XRD and SEM. Carbon electrodewaselectrochemically characterized using cyclic voltammetry (CV). A highest capacitance of 110 F/g was observed in 30 wt% H2SO4.

Jan 1, 2006

By Tor Lindstad

Specific C02-emissions are given for the production of silicon-metal, ferrosilicon, ferromanganese and silicomanganese. Emissions taken into account come from reduction materials, from coke production and generation of electric energy. C02-emissions can be abated by direct and by indirect methods. A direct method is to replace fossil carbon as reduction material wholly or partially by endogenous carbon (biocarbon, charcoal). Another possibility is to produce metals by electrolysis instead of the present electric smelting furnace. Indirectly CO2-emissions can be reduced by energy recovery, thus saving coal, oil or natural gas for heat generation. Some reduction in global C02-emissions can be obtained by giving credit for the use of silica dust partially replacing cement in concrete. In addition to give an overview of possible methods, costs will be discussed.

Jan 1, 1999

By Florian Kongoli

Minor components and flux additions can modify the liquidus temperatures of multicomponent slags. In industrial practice, slags with various levels of minor components require various flux additions in order to achieve the lowest possible liquidus temperature The prediction and the optimization of these combinations can decrease the cost of the overall process. In this work the effect of several minor components and flux additions such as Al2O3, MgO, and CaO, on the liquidus temperatures of multicomponent iron-silicate slags has been analyzed in terms of a thermodynamic model Various simple isothermal and non-isothermal diagrams are presented. These diagrams can be used directly by the process operators to define the optimum conditions under which the fluxes can be used to achieve the desired slag liquidus temperatures.

Jan 1, 1999

By David C. Lynch

FeCl3 particulate of 10 to 100 um in diameter was reacted with radicals produced in an oxygen plasma at pressures between 1 to 20 Torr. The particulate, in a fluidized bed, was positioned above the plasma to avoid over heating the oxide product which is known to lead to crust and clinker formation[ 1 ]. Reaction between the iron chloride and the gas phase occurred at temperatures between 66 and 226 °C. Oxygen radicals react with the surface material to a depth of approximately 2.5 4m. Surface material, analyzed with a x-ray technique, indicates that the maximum amount of FeCl3 reacted on a weight basis was found to be approximately 67%. More typically, 40 to 50 wt% of the chloride was reacted within 30 minutes to 1 hour.

Jan 1, 1996

By Takeshi Yoshikawa

For the development of low-cost silicon refining process for solar cells, the present authors have been studying the low temperature refining technique, ?solidification refining of Si with Si-Al melts at 1173 ? 1273K?. In the present work, we have investigated the B removal in that refining, utilizing the segregation effect and also the effect of Ti addition to the melt. Segregation ratio of B between solid Si and Si-Al melt was measured by the temperature gradient zone melting technique and it indicated the B removal fraction would be as much as 90%. Titanium addition to the melt was found to produce the TiB2 precipitation with soluble B in that melt and bring the effective B removal of refined Si to its content of 1ppma.

Jan 1, 2006

By O. Kitamura, H. Kubota

The Harima Works started its ISP operation in 1966 and been expanding its production capacity from 3,000 tonne Zn/month and 1,500 tonne Pb/month to 7,500 tonne Zn/month and 2,500 tonne Pb/month. It is not only treating zinc, lead and bulk concentrates but also secondary materials like Waelz kiln oxide from the Shisaka Works of Sumitomo Metal Mining, waste treatment sludges, industrial wastes and others. Its final products cover Prime Western Grade (PWG) zinc, Special High Grade (SHG) zinc, continuous galvanizing grade zinc, electrolytic lead, cadmium, indium, thallium and sulfuric acid. This paper briefly describes the smelter's historical and present operations. The key data for the current impurity control management and for the distribution of impurities such as copper, iron and arsenic are presented.

Jan 1, 2000

By Goren Lindkvist

Elkem has a small industrial scale. Muti-Purpose furnace at the MEFOS Metallurgical Research Facility in Lulea, Sweden. The furnace is 2 meters in diameter with installed power of 4.8 MVA, equipped with oil coiled freeze lining, gas tight electrode seals and feed chutes and a slag flow control for continuous tapping. During tests in June, 1991, the furnace was continuously operated on a high silica slag at loads from 1.5 to 4,0 MW. The slag was then charges to a low silica, high iron and lime composition. Steel plant dust was added, smelted and reduced. The slag was made more ceramic by adding alumobrick and alumina. Data from the start-up and initial operating phase of the, Elkem EAF dust plant at Laclede Steel will also reviewed.

Jan 1, 1992

By Chang Wei, Zhigan Deng, Yizhao WANG, Cunxiong Li, Gang Fan, Xingbin Li

During the process of hematite precipitation, the transformation of Na jarosite convert into hematite has been studied in a batch reactor at different temperatures, ranging from 170°C to 200°C with 3h of the retention time in the presence of 30g/L Fe ( ) and 4g/L Na+. The composition of precipitation was seriously depended on the temperature, at 170°C hematite and sodium jarosite are the reaction products of iron precipitate, with an increasing in reaction temperature the sodium, sulfur content in precipitated decreased and sulfur mainly exist in forms of SO4 2-, and when temperature over 200°C hematite was the only phase in product. An increasing temperature was not only beneficial to iron precipitation, also conducive to jarosite conversion to form high quality hematite precipitate.

Jan 1, 2016