Search Documents

By A. V. Tarasov

In order to improve the efficiency of hydrometallurgical processing of pyrrhotite concentrates, an integrated set of research has been carried out to investigate the use of sulfur dioxide in individual unit operations and as a leaching agent in the autoclave process as a substitute for oxygen. Treating iron-containing raw materials for production of nonferrous metals are based on the selective reaction of SO2 with iron sulfides and oxides. Iron is dissolved as sulfate, which can be treated in a separate circuit to produce iron-containing pigments or it can be disposed of after neutralization. Nonferrous and precious metals contained in pyrrhotite concentrate do not react with sulfur dioxide and remain virtually completely in the solid phase, i.e. high-grade sulfide concentrate to be treated by hydro- or pyrometallurgical methods. Elemental sulfur formed in the process of leaching is separated from the pulp in granulated form as a result of the use of special surfactants. The process of sulfide concentrate leaching with the use of sulfur dioxide is conducted at temperatures above the sulfur melting point (119°C) with distributed feeding of surfactant and under a partial pressure of sulfur dioxide of up to 0.3 to 0.5 MPa.

Jan 1, 2006

By Xiangru Chen, Qijie Zhai, Wei Zhang, Haicheng Li, Chao Yang

In this paper, ductile iron material with different content of niobium was prepared by a scientific melting method. Image Analysis Software was used to studied the effect of niobium microalloying on both pearlite content and pearlite lamellar spacing in ductile iron quantitatively. The results showed that the addition of a small amount of niobium could increase the pearlite content and decrease pearlite lamellar spacing of ductile iron effectively.

Jan 1, 2015

By A. H. Rosenberger, M. A. Tschopp, M. A. Groeber, K. N. Solanki, A. L. Oppedai, J. D. Miller

"Characterizing the spacing of primary dendrite arms in directionally-solidified microstructures is an important step for developing process-structure-property relationships by enabling the quantification of (i) the influence of processing on microstructure and (ii) the influence of microstructure on properties. The research objective herein is to evaluate the capability of various conventional approaches, as well as new or modified approaches, for spatial point pattern analysis with application to characterizing experimental dendritic microstructures. Both computer-generated and experimental dendritic microstructures are used for this analysis along with numerous techniques based on the nearest neighbor spacing, Voronoi tessellation, Delaunay triangulation, or graph theory. Comparison of new metrics with traditional primary dendrite arm spacing metrics will also be discussed for both local and global measures. The current methods investigated will supply information of local spacing and coordination number while addressing edge effects, parameter sensitivity, and correlation with interdendritic features, thus providing insight into how processing affects properties.IntroductionDeveloping an enhanced understanding of mechanical behavior in materials relies upon sufficiently characterizing microstructure details at the relevant length scales that contribute to this behavior. Moreover, to truly enhance the predictive capability of processing-structureproperty models that aim to improve material performance requires a quantitative description of the relevant microstructure features and, thereby, the material itself"

Jan 1, 2013

By B. J. Beaudry

The preparation of alloys containing one to two percent of the volatile lanthanide metals Sm, Eu, Tm and Yb in the high melting point (HMP) rare earth metals Sc, Y and Lu was accomplished by a vapor deposition, diffusion method without crucible contamination. The method avoids the melting of the HMP metals which would introduce impurities from the crucible, generally Ta or W. Plates of the HMP metals were hung from the lid in the upper part of the Ta crucible. The volatile metals were placed on the bottom and the lid welded in place under an atmosphere of helium. By proper selection of thee alloying temperature, the effusion of the metal vapors, through the helium atmosphere was slow enough to permit diffusion to occur and prevent refluxing of the newly formed alloy. Very volatile metals such as Mg required a Knudsen cell with a suitably sized hole to prevent too rapid transfer of the low melting metal. Electron microprobe analysis of a cross-section of the HMP metals showed a homogeneous distribution of the volatile metals. The time and temperature required to obtain a homogeneous rare earth alloy without contamination are given. The use of a Knudsen cell to form magnesium-rare earth alloys is reviewed.

Jan 1, 1992

By Esa J. Peuraniemi

Copper smelting to form blister in one single step has been possible for a long time even from low grade concentrates. In spite of obvious benefits, it has been economically viable only with few special raw materials having high enough Cu/Fe and Cu/S ratio. Outokumpu Blister Flash Smelting is currently applied at three operations, and three others will be commissioned in the near future. With typical chalcopyrite concentrates two main obstacles have prevented wider adaptation of direct blister processing: slag formation and heat generation. Oxygen potential in the reaction shaft must be high in order to produce blister with targeted sulfur content below 1%. When large amount of iron is oxidized, as well as sulfur, copper is inevitably also oxidized into slag. High copper amount in substantial tonnages of slag lead on to costly down stream recovery operations to obtain discardable slag. Almost complete oxidation of sulfur and iron releases a high amount of heat which traditionally has been solved by lowering oxygen enrichment of the blast leading on to oversized off-gas line and acid plant. One challenge in direct blister smelting relates to the attack of aggressive high-copper containing slag against furnace refractory lining. In continuously operated Outokumpu Direct Blister Flash Smelting this is taken care of by preventing vigorous melt movement in the settler. Stable bath conditions and stationary slag against refractory lining enable the formation of a protective autogenous layer between aggressive slag and vulnerable refractory. These direct blister smelting challenges are addressed from equipment and process development point of view. New solutions to overcome the obstacles are presented and discussed.

Jan 1, 2006

By Milance Mitovski, Milorad Cirkovic, Vlastimir Trujic, Dragana Živkovic

"In this article, it is analysed the possibilitis and the effects utility waste energy of process sulfuric acid production in the existing technical-technological conditions. The utility second process energy, reduction the fuels consumption, reduction environment pollution and its effects are shown, too. High heat quantity is produced as the result of exothermal reactions in the production process of sulfuric acid in Bor. A part of this heat is sufficient for the process development, and significant part of this heat presents low-temperature heat energy that is irretrievable lost. Investigations were carried out based on production of 485 t of monohydrate/day of sulfuric acid. By recovery of this heat quantity for heating purposes, about 20.000 – 25.000 t of coal/year would be saved, what would significantly improve the power efficiency of the smelter copper production. IntroductionTechnological process of copper production in RTB BOR (Serbia) produces a significant quantities of high temperature secondary (waste) heat energy that is uncontrolled “lost” in the vicinity. Secondary heat energy is produced in pyrometallurgical copper production in quantity of 1,621 kWth/kg of dry concentrate or existing heat (that presents a difference of heat at furnace outlet and heat at temperature over temperature of dew point of sulphuric acid gases) in quantity of 1,315 kWth/kg of dry concentrate. For designed capacity of Copper Smelter in Bor, the existing heat power of secondary energy is 92,111 MWt, what is an equivalent to the power of steam-turbo plant where the Rankine-Clausius heating cycle is done, and that is 28,334 MWe."

Jan 1, 2008

By M. Urda-Kiel

Stainless steel is increasingly used as a cathode starting sheet. It was shown earlier that even when depositing copper on copper, a substrate-influenced zone appears in the deposit structure, followed by a transition zone and finally by the electrolysis-influenced structure. On copper, the substrate-influenced zone has a thickness of twenty micrometers and on titanium, eventually more than fifty micrometers. Initial nucleation and growth have a considerable influence. In this paper, copper was deposited in a channel cell on four different 304 stainless steel substrates: mechanically polished and anodized, respectively, at 0, +400 and +800 mV/SHE in 1M H2SO4 at 20°C. Copper was deposited under electrowinning conditions after solvent extraction (SX) (40 g/l Cu++, 180 gh/l, H2SO4, 20 or 60°C). The results showed that, although Auger surface analyses of the substrates were only slightly different one from another including the oxide thickness, nucleation and initial stages of growth were very sensitive to the surface treatment of the substrate. Potential step and current step methods gave similar results : progressive nucleation followed by 3D diffusion controlled growth. The highest nucleation frequency was observed on stainless steel anodized at 0 mV/SHE, under various electrolysis conditions. The potential influence of these findings on industrial practice is discussed.

Jan 1, 1999

By Xiang Zhu

Xidagou is the largest waste water discharge channel of the Anshan Iron and Steel Complex (AISC) with average flow rate of 8000 cubic meters per hour, which is about 75% of the total effluent of the AISC. The waste water from Xidagou seriously polluted the Taizi River Basin. In order to meet the Chinese Class V Standard for Surface Water Discharge and the Standard for Recycled Industrial Water Reuse, with the aid of the World Bank, the AISC began the treatability studies in 1991. Based on the bench-scale test, the AISC carried out pilot-scale treatability studies on three different treatment processes and five different chemical coagulants for more than half a year in 1992. The study results show that the processes of primary sedimentation- chemical mixing and flocculation-secondary sedimentation-filtration can meet the requirement and that PFS and PAM are effective and economic chemical coagulants.

Jan 1, 1994

By Toshiyuki Kozuka

CdTe metal composite semi-conducting material has high potential in good performance of energy conversion efficiency for solar cell and there is much room for improvement of the performance by developing a process of making a thin CdTe film. In this paper, the imposition of intense magnetic field on CdTe electro-depositing surface is proposed, which is one of the possibilities for improving the energy conversion efficiency. In the experiment, cryogen-free super-conducting magnet up to 5T was used and CdTe film was deposited electrically in -0.72V vs. SHE The electrolyte was Cd and Te ammonia alkali solution with controlled temperature in the acrylic cell of 70mm diameter. Electro-deposition behavior of CdTe has affected by the imposition of the intense magnetic field due to microscopic convection in the vicinity of the depositing surface. Electro-deposited surface of CdTe becomes smooth due to microscopic convection around the surface, and the crystallization behavior is also affected, where crystallization temperature and the grain size is changed by the imposition of intense magnetic field.

Jan 1, 2003

By Antonio Luraschi

The constituents iron, oxygen, silica and cop- per are of principal interest in slags utilized in pyrornetallurgical processes for producing copper. Accordingly, phase relationships in the.Cu-Fe-0-SiO2 system are important when one considers the physico- chemical behavior of slags. These phase relation- ships for the quaternary and constituent ternary systems are developed from available information. Isothermal composition and composition-oxygen potential diagrams, and oxygen potential-temperature diagrams are utilized to describe the' important relationships.

Jan 1, 1976

By Laurentiu Nastac

"The importance of investigating solute redistribution during the unidirectional solidification of multi-component alloys is broadly discussed in the literature. A previously developed analytical model that was experimentally validated for Al-Cu, Sn- Bi and Fe-Si dilute binary alloy systems is used in this article to study in detail the solute redistribution, the liquid/solid interface stability based on an extended transient constitutional undercooling criterion and the size of the initial transient region during the unidirectional solidification of Ti-6-4 and Ti-17 alloys. A comparison between Ti-6-4 and Ti-17 alloy systems with respect to interface stability and the size of the initial transient region is also provided. The effective partition coefficients of the alloying elements in these alloys were determined based on specially designed experimental measurements.IntroductionThe importance of investigating solute redistribution during alloy solidification is broadly discussed in the literature [1-5]. One of the relevant applications of this study would be the mathematical modeling of equiaxed and columnar solidification of multicomponent alloys. This includes the instability of the solid/liquid interface. There are several mass and heat transfer processes that involve the calculation of solute redistribution during directional solidification such as industrial directional solidification processes, continuous casting, remelting processes, Czochralski crystal growth technique, floating zone techniques, etc."

Jan 1, 2012

By J. E. Dutrizac

The behaviour of the lanthanide elements during the precipitation of sodium and potassium jarosites at 98oC from sulphate media was systematically investigated. The lower atomic weight lanthanide elements (La to Gd) are characterized by the limited solubility of their alkali-lanthanide sulphates, such as NaNd(SO4)2?H2O, which commonly contaminate the jarosite precipitates. Hence, single phase jarosite-type compounds were precipitated only from solutions containing <0.4 g/L of the La to Sm lanthanides. The sulphates of the heavier atomic weight lanthanide elements (Tb to Lu) have significantly higher solubilities such that solutions containing up to 10 g/L of the individual lanthanides could be investigated without the precipitation of alkali-lanthanide sulphate species. Even at the highest lanthanide concentrations, however, none of the jarosite precipitates incorporated more than 0.3 wt% of any of the lanthanide elements. Comparable levels of lanthanide incorporation were noted in both Na-jarosite and K-jarosite. Although the mass of the jarosite precipitate increased with increasing ferric sulphate concentration or with increasing pH, the extent of lanthanide incorporation was not significantly affected. Clearly, the trivalent lanthanide elements do not substitute extensively for trivalent iron in the jarosite structure. This behaviour likely reflects the significantly lower hydrolyzability and larger size of the trivalent lanthanide ions relative to ferric ions.

Jan 1, 2003

By In-Ho Chi

In copper metallization, resistivity of copper seed layer is very important since the thickness of seed layer is less than 200iun. Conventionally MOCVD has been used for this purpose however electroless copper plating is simple process and the resistivity of copper deposit is less than that of copper prepared by MOCVD. In this study eIectroless depositions of copper were conducted on different substrate to find optimum conditions of electroless copper plating for electronic applications. To find optimum conditions, the effects and selectivity of activation method on several substrates were investigated. The effects of copper bath composition on morphology were investigated. The effects of pH and stabilizer on deposition rate was investigated. The resistivity of copper with thickness was also measured.

Jan 1, 2001

By Tiejun Chun, Jian Pan, Deqing Zhu, Zhiyong Ruan

"In this paper, the desulfuration of pyrite cinder pellets was carried out. Phase analysis shows that most sulfur of pyrite cinder exists in the form of elementary sulfur. Most sulfur was removed in preheating stage. 81.25% sulfur was removed and the average SO2 concentration of exhaust gas was 1365ppm when the pellets were preheated at 950oC for 9 min. The final product, assaying 62.42wt%Fe and 0.02wt%S content at 96.88% desulfuration was achieved under the conditions of preheating at 950? for 9 min and roasting at 1200? for 15 min, which can be used as the burden for blast furnace.IntroductionPyrite cinder, as a subsidiary product of sulfuric acid production by roasting of pyrite ores, was solid waste in sulfuric acid enterprises. According to the statistics, the annual production of pyrite cinder is about 15 million tons in China. Besides, there is lots of pyrite cinder deposited for many years [1-3]. The pyrite cinder consumed in the cement and other industries as auxiliary additives only accounts for less 30% of its total discharge and the left is stored in waste pond, occupying much land and polluting environment in China [4-5]. Moreover, pyrite cinder contains iron between 30-63% which can be utilized as a cheap raw material for ironmaking by sintering or pelletizing processes, which can not only prevent pollution but also provide cheap raw materials for ironmaking [6-7]. However, compared to traditional iron ore concentrate, pyrite cinder possesses higher sulfur content."

Jan 1, 2012

By Yapeng Zhang, Zhiwen Shi, Chaoquan Yao, Fei Wang, Xinyu Li, Jianliang Zhang

A great deal of iron ores which have special elements have been applied in the sintering process with the decreasing of high-grade quality iron ores resources. In this paper, the laterite nickel ores were added into three different kinds of iron ores respectively to make liquid phase formation research by software of Factsage and high temperature characteristic sintering experiments. The results showed that the adding proportion of laterite nickel ores should be less than 15% when the high temperature properties of the mixing ores were well. Increasing the mixing ration of laterite nickel ores in the sintering blending would play an important role in the reduction of the sintering cost.

Jan 1, 2015

By Andrew Shabalin, Vladimir Skorohodov, Svetlana Babaeva, ?lga Makovskaya

"At processing of some kinds of wastes (electronic scrap, secondary materials, spent nuclear fuel) in nitric acid solutions, and also in technology of silver refining, the significant amounts of palladium and platinum passes into a solution. The ion-exchange concentration of palladium and platinum in nitric acid solutions (5-500/dm3) are investigated. More than 30 various classes of ionites are tested. The most chemically resistance resins at the given conditions are identified. It is shown, that the maximum sorptive capacity to studied metals at high acidity the complexing, synthetic and inorganic sorbents possess. To definition of platinum metals sorption optimum conditions the kinetics is studied, isotherms of a sorption at various parameters from nitrate solutions are obtained. The conditions of the platinum and a palladium desorption from the pregnant sorbents and its regeneration with the subsequent reuse of materials were defined. The raw materials containing precious metals have very diverse composition and physical properties. Commonly the materials are processed by hydrometallurgical way. If gold or PGMs there are in raw materials to its opening hydrochloric acid solutions are applied. As an oxidizer nitric acid, hydrogen peroxide, gaseous chlorine, etc are used. Nevertheless, at processing of argentiferous materials and preliminary treatment of a waste including the spent nuclear fuel, nitric acid solutions are often used and the specified metals in some extent pass into solution [1]. Therefore selective extraction of PGMs from nitrate solutions is an actual problem. In the present work the ion-exchange concentrations of palladium and platinum in nitric acid solutions (5-500 g/dm3) are investigated. At the testing more than 30 various classes of ionites the most chemically resistance resins at the given conditions are identified. These resins are synthesized on the base of polyacrylate, styrene-divinylbenzene and vinylpyridine. For a selection of the most effective resin among what are made in Russia and overseas, a number of ionites with various functional groups were studied. Influence of functional groups type on a PGM sorption is shown for extraction of a palladium as an example (table 1). The presented data shows, that palladium concentration in a phase of ionites depends on sorbent type. If the increasing of solution acidity essentially reduces palladium sorption by sulfonic cation-exchange resins (KU-2×8) than its sorption by strongly basic anionites is approximately equal. Intermediate position is occupied by complexing sorbents. The latter (AN-31, SN-3, ANKB-35, Lewatit TP 207, Purolite S 930) are the most effective for extraction of PGMs from nitrate solutions from the point of view of capacity value. According to [2], solution behavior of Pt (II) and Pd (II) are similar. As is known from coordination chemistry, ligand environment of the metal ions substantially impacts to character of electronic spectra. The figure 1 shows the results of measurements of optical density of platinum bearing solutions with various concentration of nitric acid at ?=400 nanometers"

Jan 1, 2008

By Chonghe Li, Xionggang Lu, Wei Xiao, Xingli Zou, Weizhong Ding

The reduction degree and rate of the initial ilmenite concentrate and pre-oxidation samples by hydrogen were investigated by using thermogravimetric analysis system. H2-TPR was used to detected reduction properties of the pre-oxidation products which were oxidized at different temperatures. The phase transformations and micromorphology changes during pre-oxidation and hydrogen reduction were identified by XRD and SEM. The FeTiO3 was decomposed into TiO2 and Fe2O3 at the temperature below 900 oC. With the temperature rising, Fe2TiO5 was the only stable phase in high temperatures. The reduction of pre-oxidation ilmenite concentrate was faster than the natural sample, which was attributed to the micropores generated on the surface of ilmenite concentrate during oxidation. The main phases of the reduction product were metallic iron, ferrous pseuodbrookite.

Jan 1, 2014

By John P. Hager

One possible approach for the recovery of mercury from acid plant blow-down sludge in smelters is the use of a vacuum retort reactor for the vaporization of the mercury with subsequent collection of metallic mercury in an attached condenser. An experimental study was undertaken to investigate the vaporization of mercury when present as a compound in the Hg-S-O and Hg-Se systems. A transpiration reactor was modified to operate under reduced pressure and with a continuous flow of inert sweep gas. A water-cooled cold finger was inserted into the exit end of the reactor to provide for the rapid quenching of the exit gases and the collection of the mercury. Rates of vaporization were measured at several temperatures for each compound and were generally found to be constant at a given temperature and reactor pressure. The results were used to determine the minimum operating temperature for 100% vaporization of the compound in 60 minutes. For Hg2SO4, HgSO4, and HgSO/2HgO the required temperatures. for a reactor pressure of 50 Torr. were determined to be 634°, 622°. and 603°C. respectively. For HgO, HgSe, and HgS the required temperatures were 557°. 451°. And 382°C. respectively. For HgS the rate of vaporization was also measured at a reactor pressure of 1 00 Torr. The rate of vaporization was found to be slower resulting in an increased vaporization temperature of 423°C. It was also determined that the mercury vapor present in the exit gas stream can back-react with the other gas species to a significant extent and can result in very little condensed metallic mercury. For the vaporization of both HgS and HgSe. the mercury vapor was found to have back-reacted to the extent that virtually none of the vaporized mercury was collected in metallic form. For the vaporization of Hg2S04? HgS04, and HgSO4*2HgO the amount of metallic mercury recovered varied from approximately 50% for HgS04*2HgO to approximately 10% for Hg2S04 and HgS04. Only for HgO was the recovered mercury in primarily elemental form. The application of the results to the operation of a vacuum retort and condenser system is discussed.

Jan 1, 2001

By Satoshi Yamashita, Noboru Masuko

"Newly prepared bipolar membrane is promising to become a key material of an electrolyser for a production process of strong reducing solvent. This research is basic research for using bipolar membranes as electrolysers of reducing agents, Cr(II), TI(III) and V (II) on the laboratory scale. In this report, a bipolar membrane was tried with an electrolyser, reducing chromic chloride to chromous chloride. An analysis of mass balance demonstrates advantages of it over the former electrolyser equipped with an anion and/or. cation exchange membrane. The effects of current density and concentration of Cr(lll) on the reduction rate of Cr(II) and the current efficiency were examined No deterioration of the bipolar membrane resulted from the electrolytic reduction of Cr(III). IntroductionRecently, bipolar membrane that was the development subject for a long time in the industry of ion exchange membranes has met the stage of the practical application at last [l]. The expectation of the application to the hydrometallurgy field increases. We took up the manufacturing of the strong reducibility solvent as part of the application of bipolar membrane to hydrometallurgy technology. This laboratory has much experience in the electrolytic reduction of Cr (II) aqueous .solution such as chromous sulfateusing bipolar membrane were compared in theory to chromous chloride aqueous solution manufacturing of the strong reducibility solvent. The advantage of applying bipolar membrane by substituting ion exchange membrane is described, and the experimental result is reported."

Jan 1, 2000

By Zhou Aiping, Lv Guozhi, Niu Liping, Wang Wenbo, Zhang Ting’an, Jiang Xiaoli

The current method used to produce sponge titanium utilizes a process cycle of magnesium metal and chlorine gas via the electrolysis of magnesium chloride. The primary issues are the high capital cost of the electrolysis process and the environmental regulations limiting high chloride concentrations. Thus, the authors have developed a conceptual method involving theelectrolysis of magnesium chloride as well as a reduction process which allows for a cycle of magnesium and chloride. In the new method, MgCl2 which was distilled during the titanium extracting process as raw material was directly pyrolyzed at elevated temperatures yielding high purity magnesium oxide and chlorine. The resulting magnesium oxide can be used in the production of magnesium metal. This work examines and compares the energy consumption and economic benefits of the Kroll method as well as the new proposed method. The results from the study demonstrated that in comparison to the traditional Kroll method, the new method provided considerable economic and environmental benefits.

Jan 1, 2014