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By W. G. Davenport

Chapter 4 examined Inco (oxygen) flash smelting of pure chalcopyrite concentrate. It showed that the oxygen and flux requirements for auto thermal smelting are readily determined by a matrix calculation. This chapter extends this matrix approach by applying it to a multi-mineral concentrate.

Jan 1, 2001

By Jiann-Yang Hwang, Ying Qin, Shu-Jing Zhu

Metallurgical Oil Sludge (MOS) is a byproduct created in the process of steelmaking. More than a million tons of MOS are generated each year throughout the world. The material contains hazardous components such as heavy metals and pathogenic organics, which can cause serious environmental problems and health issues. Landfill, combustion, and pyrolysis have been investigated for the disposal of MOS. However, these methods are unsatisfactory since they are unable to reach the clean environment goal. In this study, we investigate the possibility of using MOS as a reductant in a high temperature metallurgical process. The results are reported and discussed.

Jan 1, 2015

By V. V. Geikhman

The paper updates the Plant experience in the development and implementation of an advanced environmentally friendly zinc production technology complying with the technological and economic level of producers in the world and the standards of maximum permissible gas emissions stipulated by the Russian legislation. General water recycling engineering allowed to ensure 95.6% water rotation level. All solid wastes formed during treating zinc concentrate are processed into marketable products or semiproducts and sold. As a result of implementing innovation techniques production at the Chelyabinsk Zinc Plant is non-waste.

Jan 1, 2006

By Wilky Desrosin, Alicia E. Ares, Carlos E. Schvezov

"In the present research the horizontal directional solidification Zn-Sn alloys (Zn-4wt. %Sn, Zn- 6wt. %Sn, Zn-10wt.%Sn and Zn-30wt.%Sn) was carried out by extracting heat in two opposite directions. For this purpose, ceramic molds, a muffie, a horizontal furnace with two heat extraction systems at the ends, a measurement, acquisition and recording temperature system, eight K-type thermocouples and an electronic recorder were used. The main parameters involved in the columnar-to-equiaxed transition, CET, were: the moment of start and end of solidification at each position under consideration, cooling rates, the average temperature gradients and critical temperature gradients at the CET, the average speed of liquid and solid interphases left and right, advancing in opposite directions. Also, solidification kinetics was found to be different between horizontal solidification two-way heat extractions, with preliminary results of the vertical unidirectional solidification. In the solidification experiments, the velocity and accelerations of the liquidus and solidus interphases usually occurs at the end solidification zone of the samples.IntroductionSolidification of metal alloys, which starts in the external equiaxed region (chill), results in two basic types of structures in a single solidified alloy sample: columnar and equiaxed. The presence of both structures indicates the occurrence of the colunmar-to-equiaxed transition phenomenon[!].Studying the colunmar-to-equiaxed transition, CET, is of great technological interest for the evaluation and design of the mechanical properties of the solidification products. To this end it is necessary to understand the mechanisms by which it occurs. As found in previous studies [2-5], the CET occurs by competition between columnar and equiaxed growth. Mainly is controlled by the parameters of casting, such as the alloy composition, the density of the present nuclei in the liquid, the cooling capacity of the metal I mold, and the degree of convection in the liquid [7-10]."

Jan 1, 2014

By T. Shoji

"The human history is characterized by social development based on mineral and energy resources, and many conflicts to take the resources by power. This is shown by not only world wars but also many local conflicts as well as international supremacy.IntroductionThe world population after B. C. 10000, which is summarized in several papers, is approximated by four straight lines on a semilogarithmic diagram as shown in Figure 1 [l]. The annual rates of increasing are 0.0041, 0.071, 0.53, and 1.85 % from the old and young periods. The boundaries among four periods are approximately B. C. 4600, AD. 1670, and 1930. The start of the second period seems to correspond to the beginning of agriculture and cattle breeding. Precisely speaking, the usage of natural energy resources such as woods and domestic animals already began, but is inferred to have become common after the age. The third and fourth periods are characterized by the common usage of coal and oil, respectivety. Not only energy resources but also mineral resources including gold, copper, iron and others are also important for the human history.Mineral and energy resources have supported the development of the .human civilization, and have caused many conflicts because of this reason. Every day newspapers report conflicts, such as Chechnya, East Timor and Ache. We can easily point out the facts that the conflicts closely relate to mineral and energy resources. Groznyj, Capital of Chechnya, is located on the western margin of Caspian oil field. Many mineral deposits occur in Kavkaz Mountains running south of Chechnya. Subsea oil fields occur in Timor Gap located between East Timor and Australia. Ache is also one of oil fields in Indonesia. It is very difficult to state present conflicts independently of a political view of point. For this reason let us try to historically review the relation between mineral and energy resources and international domination and conflicts [2] based on many papers [3]."

Jan 1, 2000

By Nobuhiro Ishikawa

The in-situ observation of the effect of impurities on the reduction process of iron oxides by C in TEM was carried out. A few wt% of CaO or AbO, was used as impurities in FeO was prepared. Some precipitates grew into the C layer expect for using 3.0wtCa. The reaction between FeO and carbon was much different from using pure FeO at about 800-1 lOOK. The rate of reaction became much slower including Ca and almost no reaction was happened with the concentration of CaO up to 3.0wt%. On the contrary, AbO, had ahuost no effect on the reaction. The results indicated that Ca suppressed the reaction and the effect of Al was much less. The precipitates which grew into C layer accompanied almost no Ca and AI. Only Fe was detected in the precipitates.

Jan 1, 2008

By Jonkion M. Font

An expression for the distribution ratio of arsenic between slag and copper matte or liquid copper was developed by both, an extension of the Reddy-Blander moderl for deriving a priori the arsenic capacity, and by a relationship between the arsenic capacity and the arsenic distribution ratio. In this study, the a priori arsenic capacities in the FeO-SiO2, CaO-SiO2,MgO-SiO2, FeO-CaO-SiO2, FeO1.5-CuO0.5-MgO-SiO2, FeO-FeO1.5-CuO0.5-CaO-Mgo and FeO-FeO1.5-CuO0.5-CaO-Mgo-SiO2, slags were calculated at 1573 K. The a priori arsenic distribution ratio between the FeO-FeO1.5-CuO0.5-CaO-MgO-SiO2 slag and copper matte mn (Lx, )' and between the FeO-FeO1.5-SiO2 or FeO-FeO1.5-CuO0.5*-CaO-Mgo slag and liquid copper (Ls/cua) were calculated. The model calculated data are found to be in good agreement with the reported experimental data. The availability of reliable thermodynamic data for slag components and impurities in the slag-matte- metal system is essential for the accurate prediction of impurity capacities and distribution ratio data. The arsenic distribution ratio model developed here, can be extended for predication in multi-componet slags and mattes or liquid metal, and thereby may lead to the development of new slag systems for the efficient removal of arsenic in the copper smelting, converting and refining processes,

Jan 1, 2003

By Sepp Härkki

The energy crisis in Finland after World War I1 together with a sharp rise in the price of energy caused Outokumpu Oy to consider replacing the electric furnace smelting of copper concentrates by some other method. The flash smelting method developed under these circumstances offered a considerable saving of fuel through the utilization of the reaction heat of sulphides and yielded a high recovery of sulphur in the form of acid. The pilot plant testing of the new process was carried out in the years 1947 - 1948. The process was adopted for the smelting of copper concentrates (1) (2) (3) on a commercial scale in 1949 and applied successfullv to the smelting of -nickel concentrates' at the Harjavalta Works in 1959 (4) (5) (6). In 1962 Outokumpu adopted another type of flash smelting where elemental sulphur is recovered from the gases after the thermal decomposition of pyrite in the flash smelting furnace (7) (8): In recent years, the copper-nickel flash smelter and pyrite process have been combined to produce elemental sulphur instead of SO2 from the smelter gases (9) (10). The basic idea of the Outokumpu flash smelting process for sulphidic ores is that the conventional methods with separate roasting and smelting operations are replaced by a combined roasting, smelting and part-converting process carried out in one unit. The heat generated from the exothermic reactions can thus be used for smelting the ore so that only a small amount of additional fuel is needed. The characteristic of the method is also that the dried, fine-grained concentrate is smelted in suspension, which offers the best conditions for rapid reactions. The recovery of waste heat from the furnace off-gases had been considered already in the original flash smelting system. A

Jan 1, 1976

By Duclerc Fernandes Parra, Luis Filipe Carvalho Pedroso Lima, Harumi Otaguro, Washington Luiz Oliani, Hélio Fernando Rodrigues Ferreto, Ademar Benevolo Lugao

The activation of three polyethylenes, the low density, the high density and the linear low density polyethylene, was determined by means of dynamic mechanical analysis (DMA). Storage modulus and tan δ spectra were obtained as a function of the temperature from −60 to 50 °C with a heating rate of 2° min−1 at frequencies of 1, 2 and 5 Hz and measurement strain amplitude of 10−5. In the tan δ spectra, a small peak in the β region of the three polyethylenes was found and substantiated by subtracting the growing exponential background. This procedure was based on a model that associates the dislocation motion on metals under cyclic stress to vibrating strings and considering the same for the polymeric chains. For the determination of the activation energy we have utilized the frequency versus the reciprocal of the absolute temperature peak of the tan δ. The values obtained for the three polyethylenes, the low density, the high density and the linear low density were, 362 ± 12, 266 ± 9 and 197 ± 6 kJ mol−1, respectively, which were compared with those presented in the literature.

Mar 1, 2017

By François Larouche

Since their commercialization in the early 1990s, lithium-ion batteries (LIBs) have become ubiquitous for powering a myriad of portable electronics. Their usage now extends to the automotive industry and stationary energy storage market. With an average life of 6.2 years and the strong demand, the volume of spent LIBs has increased exponentially, making recycling mandatory. Currently, recycling/ recovery of spent LIBs is limited in comparison to all other types of batteries. The current processes focus mainly on the recovery of the most valuable metals such as cobalt and nickel, leaving lithium and phosphate in a low value end-product. It is necessary that new advanced recycling technologies are developed for the recovery of spent LIBs both from an economic and environmental perspective. In this paper, the current R&D status of LIBs recycling is reviewed with the emphasis placed on hydrometallurgical processing opportunities for Li-ion and Li-solid state batteries.

By A. Arenas-Flores, Pandiyan Thangarasu, J. P. Hernández-Lara, F. R. Barrientos-Hernández, J. A. Romero-Serrano, A. Hernández-Ramírez, M. Pérez-Labra

BaTiO3 doped with Gd3+, was synthesized from BaCO3, TiO2, and Gd2O3 as powders using the solid state reaction method (Ba1-xGdxTi1-x/4O3). The milling of the precursors was performed in an agate mortar with acetone as control means and compositions x = 0.001, 0.005, 0.05, 0.15, 0.25, 0.35 Gd3+ (wt%). Firstly, the powder mixture was decarbonated at 900 °C for 8 h, after it was sintered at 1400 °C for 5 h. Tetragonality of synthesized BaTiO3 doped with Gd3+ was analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Raman spectroscopy (RS). Subsequently, the powders sintered were uniaxially compacted cold until to obtain pellets of about 10 mm in diameter; which again were sintered at 1400 °C for 4 h. XRD patterns and Raman spectra results revealed that the crystal phase of the obtained particles was predominately tetragonal BaTiO3.

Mar 1, 2017

By Donald I. Bleiwas

World primary nickel production in 1987 is projected to be 770,000 mt, slightly higher than that in 1986. Market economy country (MEC) production in 1987 is projected to be about 524,000 mt, an increase of almost 5 pct over 1986 production. Production cutbacks and closures at Japanese ferronickel plants in 1987 resulted primarily from the strong yen and higher energy prices. Cutbacks also caused reductions in ore production from Indonesia, New Caledonia, and the Philippines. Technical problems affected production, to varying degrees, in Botswana, Indonesia, and Yugoslavia. World primary nickel production for 1988 is projected to be 787,000 mt, of which 536,000 mt will be produced in MECs. Increased production is projected from Botswana, Canada, Cuba, and possibly Greece and Yugoslavia, while slight production decreases are projected for Indonesia, New Caledonia, the Philippines, and Zimbabwe. .. South African nickel production in 1988 could be severly curtailed by social strife. In the early 1990's Brazil and China could be major economic competitors to Western nickel producers.

Jan 1, 1988

New method for processing of copper and nickel production feed has been developed and tested at pilot unit having 10 t/hr capacity. The process allows single-stage treatment of ore feed including that with high magnesium oxide content and resulting in the production of rich matte, high-grade matte, or moralised alloy for further leaching, as well as dump slag and off-gasses suitable for production of elemental sulphur, liquid sulphur dioxide, or sulphuric acid. Tests results and principal technical and economical parameters are presented.

Jan 1, 2006

By Tao Li

The development of DP(Dual Phase) steels and TRIP(Transformation Induced Plasticity) steels has received much attention in recent years due to their high strength and simultaneous good ductility, which provides the potential for weight reduce and resource savings on certain components in automobile or other industries. So a controlled rolling process was simulated in the present study by thermomechanical simulator (Gleeble 1500) for producing DP steels on a kind of low carbon steel containing a small amount of Si and Cr. F+M dual phase microstructures have been obtained during continuous cooling processes of a wide cooling rate range from 10°C /s to 60°C /s. The grain size of the dual phase steel developed can be refined to less than 5 m through the mechanism of deformation induced ferrite (DIF) transformation. The ultrafine ferritic grains are equiaxed with high-angle boundary, and the martensite islands of an average size less than 5m disperse uniformly in the ferrite matrix. The ultrafine martensite islands not only inhibit the growth of ultrafine ferritic grains and improve the bonding of F/M interface, but also increase remarkably the strain hardening rate in the processing of the present Dual-Phase steel. As a result, the tensile strength of ultrafine grained Dual-Phase steel reaches higher than 1000 MPa. The result shows that an ultrafine grained Dual-Phase steel of low carbon and low alloy is promised to exhibit desired F+M microstructure by means of this new TMCP process.

Jan 1, 2006

By Victor Stancovski, Uday Pal, Stephen C. Britten

"An in situ electrochemical technique for measuring the concentrations of easily dissociable oxides in slags at temperatures between 1200-1600°C is being developed. The technique utilizes a partially-stabilized-zirconia solid electrolyte (PSZ), which conducts oxygen ions, to separate a reference-gas compartment from the slag of interest. Three types of measurements are currently under investigation which yield different information concerning the slag phase and hence will be combined into a single amperometric device for monitoring the properties of easily dissociable slags.Type I utilizes an open-circuit-voltage measurement between the reference gas and the slag phase. Type II utilizes a potentiostat to apply a direct current potential step or sweep between the inner and outer compartments of the electrolyte, driving oxygen ions from the slag into a reference gas. With the use of open-circuit-reference electrodes, the resulting current-potential profile reveals the dissociation potential and concentration profile of dissociable oxides such as those of iron, manganese, and chromium. Information on the transport properties of the cations can also be generated from these measurements. Type III utilizes a potentiostat with reference electrodes to carefully electrolyze a known volume of slag by removing large quantities of oxygen ions from the slag to the reference gas. The coulombs of charge removed at different applied potentials can be used as a direct indication of the concentration of each dissociable oxide species present within the slag."

Jan 1, 1997

By Lv Guozhi, Niu Liping, Liu Yan, Zhang Zhiqi, He Jicheng, Zhang Ting’an, Dou Zhihe

"CuCr alloy can be extensively used as contact materials in integrated circuit, electrodes, electric contact and high strength conductor. We proposed thermit reduction-electroslag remelting method of preparing the large scale CuCr alloy. But there are pores and oxide inclusions in CuCr alloy prepared by thermit reduction process. This paper studied mainly the effects of ratio of reactant and additive on the inclusion type and their occurrences in CuCr alloy. The slags and CuCr alloy were characterized respectively by XRD and SEM. The results show that when the additive is Na3AlF6, the slag consist of Al2O3 and Cr. When the additive is CaF2, the slag consist of Al2O3, Cr, CaF2 and CaAl4O7. The inclusions in CuCr alloy are mainly Al2O3 and pores which disperse in Cu-rich zone and Cu-Cr phase interface. When 5% CaF2 and 5% KClO3 are added, there are fewer pores and inclusions, and the more better microstructure.1 IntroduceCuCr alloy is the contact terminal material with an eximious properties[1,2], which gradually replaces CuBi alloy becoming the first choice for contact terminal material in the medium and high power vacuum switch after the 1970s. The traditional preparation methods of CuCr alloy mainly contain powder metallurgy, infiltration process and vacuum electric arc melting methods. But the above methods exist some shortcomings, such as poor product quality, high cost of production, processes complex ect[3-9]. CuCr alloy is made by the thermit reduction self-propagating method, which uses CuO, Cr2O3 and Al as raw material to get the high-temperature melt, and then casts to manufacture CuCr alloy ingot, which response equation follows as:"

Jan 1, 2012

By Dinesh Agrawal

Microwave energy has been in use for variety of applications for over 50 years. These applications include communication, food processing, wood drying, rubber vulcanization, medical therapy, polymers, etc. In the last two decades microwave heating has been also applied very effectively and efficiently to heat and sinter ceramic materials. Microwave heating is recognized for its various advantages, such as: time and energy saving, very rapid heating rates, considerably reduced processing cycle time and temperature, fine microstructures and improved mechanical properties, better product performance, etc. The most recent application of microwaves has been in the field of metallic materials for sintering, brazing/joining and melting. Several common steel compositions, pure metals and refractory metals have been sintered in microwaves to nearly full density with improved mechanical properties. Many commercial powder-metal components of various alloy compositions including iron and steel, copper, aluminum, nickel, Mo, Co, Ti, W, Sn, etc., and their alloys have also been sintered in microwaves producing better properties than their conventional counterparts by using a 2.45 GHz multimode microwave system. This work has been further extended to join and braze bulk metal pieces, especially super alloy based turbine blades. Further, in a specially designed microwave cavity, even the bulk metals can be made to couple with the microwave field and melted. The implications of these findings are obvious in the field of powder metal technology.

Jan 1, 2006

By Lenny Winkel

With the aim to develop a solar-driven process for the extraction of copper from sulfide concentrates research on the decomposition of copper sulfides under inert atmospheres has been initiated. Thermogravimetric measurements on chalcocite,(Cu2S) revealed that copper is formed already at 1823 K. Chalcopyrite (CuFeS2) also disintegrates at this temperature, although at a lower rate. Copper and iron have been identified in the solid residue. The results confirm the feasibility of copper extraction by direct decomposition of sulfides under atmospheric pressure. The decomposition under inert atmosphere prevents generation of SO2, it also alters the behavior of volatile impurities during decomposition of copper sulfide concentrates. Chemical equilibrium calculations for chalcopyrite contaminated with enargite (Cu3AsS4) have shown that the absence of an oxidic slag allows for a complete evaporation of arsenic and subsequent separation from intermediate sulfides. The need to better assess the potential of direct sulfide decomposition has prompted the development of an experimental setup for studying the decomposition reactions. The experiment has been devised such that data on the decomposition kinetics and on impurity removal can be obtained at temperatures up to 2500 K.

Jan 1, 2003

By J. Gartelmann, B. Zaslavsky, Y. Vojta, D. J. Chaiko, W. Mego, A. N. Rollins

"Aqueous biphasic extraction (ABE) processes offer the potential for low-cost, highly selective separations. This countercurrent extraction technique involves selective partitioning of either dissolved solutes or ultrafine particulates between two immiscible aqueous phases. The extraction systems that we have studied are generated by combining an aqueous salt solution with an aqueous polymer solution.We have examined a wide range of applications for ABE, including the treatment of solid and liquid nuclear wastes, decontamination of soils, and processing of mineral ores. We have also conducted fundamental studies of solution microstructure using small angle neutron scattering (SANS). In this chapter we review the physicochemical fundamentals of aqueous biphase formation and discuss the development and scaleup of ABE processes for environmental remediation.IntroductionAqueous biphasic extraction (ABE) is a highly adaptable separation technique that can be used in a wide range of applications. We have been evaluating various types of ABE systems for possible applications in the treatment of solid radioactive wastes (1,2), liquid nuclear wastes (3,4), and contaminated soils (5-7), and in the removal of organics from aqueous salt solutions (8). We have also conducted fundamental studies of the solution microstructure of ABE systems using small angle neutron scattering (SANS) (9).The extraction systems are generated by combining an aqueous salt solution and an aqueous polymer solution. This produces two distinct liquid layers that are as immiscible as oil and water, yet each liquid layer contains at least 70 to 80 wt % water. The biphasic systems that we have been working with consist of immiscible polyethylene glycol (PEG) and salt solutions. Some inorganic salts that promote biphase formation with PEG solutions include the sodium/potassium salts of sulfate, carbonate, phosphate, and hydroxide (10)."

Jan 1, 1996

By Musa Karakus

In an attempt to explain the phenomena of lead entrainment during Cu drossing of lead bullion, two different synthetic lead bullions were heated to 1050°C, cooled slowly to various temperatures, and then quenched. The morphology and composition of dross particles that form when Mn is used to desulphurize bullion also were examined. Polished sections of these pyrometallurgical products were examined by process mineralogical techniques to identify the impurity phases, determine their chemical compositions, examine the morphology of the impurity phases and evaluate the potential for lead entrainment in such crystals, and characterize pre-quench and quench-generated phases. The phases crystallized were metallic lead, metallic copper, galena, chalcocite, albandite, Cu14.4Pb2S9. and 5.5Pb2S3.5. Metallic copper formed isometric skeletal crystals, chalcocite formed platy and skeletal crystals, and 1formed crystals and eutectic intergrowth with chalcocite and Cu14.4Pb2S9 or Cu5.5Ph2S3.5. The pre-quench crystals are larger and usually exhibit skeletal forms; the quench-generated phases are only a few micrometers across and disseminated throughout the lead matrix. Skeletal crystals of metallic copper and chalcocite form three dimensional networks that entrain large amounts of metallic lead.

Jan 1, 1989