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By Farouk Tedjar

The growth of miniaturization in one hand and energy density need lead to rapid development of new chemistry for batteries as observed during last decade particularly in secondary systems. However dark side of the progress is always in environment impact and scarcity of resources. In the lithium segment a jump from six electrochemical series (all non rechargeable systems) before 1990 to more than 15 systems including new rechargeable systems has been observe during last decade. Lithium battery chemistry was enriched with new electrolytes, conductive salts and new oxide composition. In the same time, lithium ion battery safety was strongly improved during last period. The progress of these technologies was strongly boosted by the substantial growth of the mobile telephone market in the mid 1990's (+ 1% a month in 2000, and a 71% penetration rate in Europe in 2005 compared to just a few percent in 1996). This market is constantly in search of higher electrochemical performance (mainly energy density in front of increasing miniaturization. Recycling of end of life product could be managed not only in environment aspect, but also under resource conservation and economic aspect of arising technology (mainly on the effect of re-injection recovered materials) The Li-ion segment is a new branch in the cobalt market and impact of LiCoOx will be fitted with the actual increase of the demand for this battery. For this reason all the processes aim to valorize active and packaging material. RECUPYL process project was conducted in this direction to offer a new solution for recycling those lithium systems. The process has been developed at pilot industrial scales using synergy between new equipment (for mechanical pre-treatment step) and existing line at RECUPYL facility (for chemical treatment) and should lead to high valorization rate with a minimum hazardous co-products. The process was also developed in order to be able to recover news cathode materials introduced in electrode like LiFEPO4, LiMxCoyO2 and new anode composition in substitution with former carbon anode.

Jan 1, 2006

By Takaaki Ishikawa

The distribution equilibria of lead, zinc and copper between CaO-Si02-Ah03 melts and liquid copper were measured at 1623K under a controlled H2-C02 atmosphere. The distribution ratios were plotted against the oxygen partial pressure, and reasonable oxide forms dissolved in the melts were estimated from the slopes of the plots. The activity coefficients of zinc oxide (ZnO), lead oxide (PbO) and cuprous oxide (CuOQs) increased with increasing slag basicity, defined by Xcao /XSiO, The temperature dependence of the activity coefficients was also measured.

Jan 1, 2003

By H. -Peter Sattler

The laser sorting technique for replacing the handpicking of the non-ferrous metal scrap from auto shredders was first introduced 1990, The process is based on the use of atomic emission spectroscopy induced by lasers to identify the scrap particles and sort them with adequate systems into main fractions of Al-, Zn-and Cu-alloys, stainless steel and lead, In the meantime the handling technique for the scrap, i.e. the singling and sorting technique as well as the analytical detector were further developed for more efficiency and higher reliability, i,e. less maintenance, minor sorting errors etc. These developments were mainly based, on and initiated by operational experiences from the startup phase of a first production plant. Part of the on going research work was the development of an ,aluminium detector which makes it the first time possible to sort mixed aluminium scrap automatically into specific alloy fractions.

Jan 1, 1995

By M. Vondersaar, B. Bulnes

Quemetco, Inc.,. as a subsidiary of RSR Corporation, operates one of RSR's three secondary lead smelters in the City of Industry, California, next to a residential area within Los Angeles County. The Reverberatory furnace serves as the main reactor for melting lead grid and paste recovered by the battery crushing system. Feed material is introduced via screw conveyor after drying in an upstream rotary kiln. Slag produced by the Reverb flows directly to an electric arc furnace. Products from this one-pass furnace system consist of soft lead bullion from the reverb, hard lead bullion from the arc furnace, and a non-hazardous slag from the arc furnace. Furnace bullion is processed into finished product in a six-kettle refinery. An overview ·of plant operations is presented. Where applicable, references will be made to changes that have taken place during the last decade.

Jan 1, 2000

By S. Z. El-Tawil, K. A. El-Barawy, M. B. Morsi, M. M. Nasr, Z. I. Zaki

"Tue sulphatization of zinc concentrate produced from heated zinc concentrate of Um Ghieg area, eastern desert by ammonium sulphate as sulphatizing agent is carried out at different conditions to achieve the appreciable formation of soluble sulphates. The maximum zinc recovery as soluble sulphate equfils to 95% upon using 1.5 stoichiometry ammonium sulphate at 600 °C for one hour. Tue obtained leached zinc sulphate solution is subjected· to purification process to prepare high pure zinc metal and zmc compounds such as pure zinc sulphate, zinc caibonate and zinc oxide. The products obtained are analyzed chemically and identified by X-ray analysisTue mechanism and kinetics of the sulphatization process of zinc concentrate are considered where the activation energy is calculated and equals to 33.3 K.J.mol""1 A process flowsheet for the overall sulphatization process of zinc concentrate by ammonium sulphate is proposed.IntroductionConsiderable reserves of zinc ores are present in Um Ghieg area eastern desert, Egypt. The possibility of extraction zinc from these ores and preparing its valuable compounds by choosing a more feasible technology become of vital importance. An attention is focused on the sulphatizing roasting processes (1-9) to achieve the appreciable formation of soluble sulphates. Previous publications are reported in our division by El. Tawil and others (10-16) using ammonium sulphate as sulphatizing agent for the successful treatment of nonferrous bearing materials.Therefore, the present work aims to study the different factors affecting the sulphatizing roasting process of local zinc coocentrate by anunonium sulphate to extract completely zinc and preparing its main compounds. Tue mechanism and kinetics of the different chemical reactloos that 1ake place in the process are considered."

Jan 1, 2000

By O. A. Ogunseitan

The contamination of aquatic ecosystems by mercury wastes is one of the most serious forms of environmental pollution associated with the metal mining and electrochemical industries. The transformation of inorganic mercury to alkylated species is a reversible bacterially-mediated process. The production of methylated mercury is of ?major public health and eco-toxicological concern because these forms of mercury are highly toxic ?and they bioaccumulate in aquatic organisms. We determined the response of the genetic determinants of mei:cury transrormation by Pseudomonas species (that predominate in contaminated soils and sediments), to the concentration and species? or available mercurfiations. By combining selective isolation and gene. ?probe techniques, the intrinsic genetic potential for mercury detoxification in a contaminated environment ?can be estimated. We determined that genetic units required for mericury volatilization (merA ?for mercuric reductase) are naturally amplified in response to mercury. Mercury-resistant bacteria that tolerate up to 100 ug Hg(Il)/ml of medium contain about 10 times more DNA fragments encoding merA than in unadapted bacteria. The exposure of bacteria to methylated.Hg (10 ug/ml lake water) produced increases (up to 10 times) in .genetic units, and higher levels of genetic expression (up to 50 times) per ml of lake water for the mercury reductase system, than on-induced lake water. The findings suggest that in environments where methylated Hg may accumulate as a result of bacterial activity, the reverse reaction which leads to the removal of mercury through volatilization from the system, may be achieved by inducing genetic ?amplification and expression of the mercuric reductase gene system.

Jan 1, 1991

By Yoshihiko Maeda

"Although Japanese mining industry once had been a polluter of toxic heavy metals and gasses, it has been struggling for improvement of environment at mining and smelting facilities under the strict Japanese regulations. Through these efforts, the industry has developed various environmental technologies to be applied in other industries and society.Recycling of metal scraps, for example, has been conducted at smelting facilities. Treatment of hazardous waste, cleanup of contaminated soil and management of landfill are other examples of application of mining and smelting technologies and facilities. In accordance with the worldwide environmental concerns, the industry has become one of the leading industries to promote ""Sustainable Development"", and it is expected further contribution in reducing various environmental burdens to earth by utilizing its mining and smelting technologies and facilities. Some of the examples of these applications are presented in this paper.IntroductionDowa Mining Co., Ltd., established in 1984, is known as one of the ~op Japanese producer of nonferrous metals. Base on its special expertise in the mining and smelting of complex ores, it has expanded its business areas to downstream activities ranging from highly purified metals and alloys, electronics materials, chemicals and related various businesses. Dowa Mining now is becoming more active in the field of waste treatment and recycling.Dowa Mining had operated some mines until 1980th, located at the western part and northern part of Honshuu Island in Japan; the former is pyrite mine while the later is ""Black Ore"" mine,· a complex sulfide ore composed of high grade of copper,· silver, lead and zinc. However, due to the strong yen began in1985; Dowa Mining closed its mining operation in 1994, and has sifted to mining operations in Mexico."

Jan 1, 2000

By William Petruk

The primary requisite for a successful extractive metallurgy operation is to grind an ore fine enough to liberate the minerals so that they can be concentrated, or to expose mineral surfaces so that the minerals can be leached. The ease or difficulty of liberating or exposing the mineral grains is dependent upon the mineral textures such as grain size, crystallinity and bonding between mineral grains. In particular, mineral grains with straight grain boundaries and a weak bonding to other minerals are easily liberated and readily concentrated into high grade concentrates. In contrast mineral grains that have re-entrant boundaries and are strongly bonded to their neighbours are not easily liberated and will not produce high grade concentrates, even with regrinding. Similarly, inclusions that occur along fractures and grain boundaries can be readily exposed and leached. Whereas minute random inclusions in large grains will not be liberated or exposed unless they occur along planes of weakness.

Jan 1, 1995

By Rolando Campos

In August 1993, the operation of Refimet Chile's copper custom smelter commenced at La Negra, near Antofagasta in northern Chile. Design smelter throughput corresponded to 235 000 tonnes of concentrate, calcines and copper cements arising from suppliers in the north of the country to produce 90 000 t/y of blister copper. Refimet had initially gained experienced in building and operating leaching, roasting and a blast furnace facility at Rungue, near Santiago, followed by Roasting at La Negra. The initial smelter project was based on conventional reverb- smelting and Peirce-Smith converting and the majority of equipment was 'purchased second-hand and rehabilitated or modified. After only 3 years in production, the treatment capacity was significantly improved by introduction of technical improvements to the original plant operating scheme. Recently, the plant was further expanded to an annual smelting capacity in excess of 400 000 t/y feed, corresponding to around 160 000 t/y copper production. This expansion, referred to as Phase 2, was achieved by modification of the reverb to oxy-fuel firing, addition of a further (second-hand) acid plant, fire refining and anode casting facilities. Parallel development of concentrate injection into enlarged converters-also took place. Following successful commissioning of Phase 2 expansion, initial engineering studies for a third expansion phase have been completed. This aims to use leading technology based on bath smelting of bone-dry concentrates in a Continuous Reactor. This paper provides an overview of the relatively short plant history, its development and improvements together with operating indices achieved.

Jan 1, 1998

By S. G. Kumar

Experimental studies on high carbon steelmaking through LD Converter - Vacuum Arc Degassing - Bottom Pouring route to produce low oxygen steels were carried out. The results indicated that it is possible to produce steel with a total oxygen content of less than 15 ppm. Thermodynamic and mass balance calculations are made on low-carbon steels that are treated by a complex deoxidation practice based on primary deoxidation of aluminum, manganese and silicon additions; followed by secondary deoxidation of vacuum degassing with simultaneous additions of aluminum. The results showed that primary deoxidation is mainly due to aluminum and the effect of carbon under reduced pressures on deoxidation of molten steel that is already killed by aluminum is negligible. The effect of process parameters on total oxygen content of steel, like carbon content, slag composition and inert gas purging, are discussed.

Jan 1, 1994

By Alan Branham

The Mike deposit is a large, low grade, oxide, gold-copper system found at the intersection of two major faults that bound the Carlin Window, Eureka County, Nevada. Disseminated gold occurs within metamorphosed and hydrothermally altered silty limestone (Silurian-Devonian Roberts Mountains Formation), beneath 182 m (600 feet) of barren Tertiary sediments and tuffs. A supergene copper oxide blanket occurs beneath and locally overlaps the lower portion of the gold zone. Decalcification argillization, silicification, and brecciation are superimposed on earlier calcsilicate hornfels and marbles. Altered dikes and sills intrude the gold zone and are locally auriferous.

Jan 1, 1995

By Shadia J. Ikhmayies

"Cadmium telluride (CdTe) is a very interesting material that has many applications. Thin films of p-type CdTe can be used as the absorber layer in the heterojunction CdS/CdTe thin film solar cells in which n-type cadmium sulfide (CdS) works as the window layer. A review of the photoluminescence (PL) spectra ofp-type CdTe thin films prepared by different techniques was performed. The presence of defects and impurities such as oxygen and chlorine influence the PL spectrum. Copper and other dopants change the PL spectra and enhance the defects band. Chemical-heat treatment especially with CdCh is known to improve the quality of CdTe thin films because it decreases the Cd vacancies and quenches deep traps, so it enhances the PL signal. A discussion of chemical-heat treatment especially with CdCh, the effect of the ambient atmosphere, and that of the measuring temperature is performed.IntroductionCadmium telluride (CdTe) is a II-VI compound semiconductor that has a cubic zincblende (sphalerite) structure with a lattice constant of 0 A4~11]. Other than all of II -VI semiconductors, CdTe can be made both n- and p-type. But due to self compensation it is not easy to get p-type CdTe films [2]. Polycrystalline CdTe thin films are interesting because they have a lot of applications. Most of the problems associated with the use of these films are attributed to inhomogeneity, self-compensation, and the difficulty of forming a stable and lowresistivity ohmic contact [3]. CdTe technology has been established for a large number of applications, including solar cells, optical and nuclear detectors, and thermal- and radiationimaging devices [3]. At present, the highest demonstrated conversion efficiency for a CdTe based heterojunction (ID), with CdS as a window layer, is 16.5% [4, 5]. CdTe thin films can be prepared by different experimental techniques, such as thermal evaporation [l], electrochemical deposition (ED) [3], close-spaced sublimation (CSS) [3, 4, 6], physical vapor deposition (PVD) [3], chemical molecular beam deposition (CMBD) [7], and close space vapor transport (CSVT) [8].The objective of this paper is to make a review of the photoluminescence (PL) spectra ofp-type CdTe thin films prepared by different techniques and discuss the factors that influence the PL spectra. The composition of the film is very interesting in determining its PL spectrum. Different kinds of defects, impurities and dopants have their finger prints in the PL spectrum. Deposition techniques and deposition parameters such as the deposition temperature and ambient atmosphere also have their influence. Heat and chemical treatments which are known to improve crystallization and reduce the defects change the PL spectrum."

Jan 1, 2013

By Suleyman Tekeli, Serdar Salman, Bulent Aktas

"The effect of La2O3 content up to 15 wt% on phase stability, sintering and microstructure of cubic zirconia (8YSZ) was investigated. XRD results showed that the specimens containing up to 15 wt% La2O3 were composed of only cubic structure. Also, the specimens doped up to 5 wt% La2O3 revealed no La2O3 peaks, indicating that La2O3 was completely solubilized in the cubic structure. However, when> 5 wt% La2O3 was added, the peak of La2Zr2O7 compound emerged, showing that the overdoped La2O3 was not solubilized in the 8YSZ matrix. The lattice parameter of the 8YSZ slightly decreased with the increasing La2O3 content up to 1 wt% but further increase in the La203 amount resulted in an increased lattice parameter. The comparison of grain size of the 8YSZ specimens with various La2O3 content showed that grain size slightly increased with the increasing La2O3 content up to 1 wt% but further increase in the La2O3 amount resulted in a decreased grain size.IntroductionAt atmospheric pressures, three polymorphic forms of Zr02 are stable at different temperatures i.e. monoclinic, tetragonal and cubic. A high-pressure orthorhombic form of Zr02 has also been reported[l]. The successful production of pure Zr02 bodies is not possible all the time due to the large volume expansion associated with the martensitic tetragonal-monoclinic transformation. This fact restricts the applications of zirconia, in spite of its excellent mechanical and thermal properties. However, the stabilization of the high temperature polymorphs at room temperature as stable phases is made possible by addition of suitable dopants. Fully stabilized cubic Zr02 and partially stabilized tetragonal Zr02 show interesting properties and are widely used as ionic conductors, coatings and gas sensors in solid oxide fuel cells and structural applications[2]. Most frequently used dopants include Y203, CaO, MgO and Ce02, although other oxides, such as those of rare earth elements, can also act as stabilizers of the high temperature structures. The incorporation of aliovalent cations to the lattice, forming substitutional solid solutions, allows to control the concentration of anionic vacancies in the structure. This aspect is particularly important in designing ionic conductors[3], and is also determinant in the stabilization process[ 4]. The process of stabilization with larger ionic radii dopants is rationalized by the crystal chemistry model[ 5], that describes the dopant cations as typical stabilizer when they have larger ionic size, lower charged state and higher ionicity than Zr4+ The ionic radius of Zr4+ is 0.84 Å and that for La3+ is 1.016 Å [6]."

Jan 1, 2012

By Carl C. Nesbitt

A study was conducted to investigate the claims of early observers who noted an increase in the rate of gold dissolution when chlorine was chemically produced in the leach vessel compared to sparging with chlorine gas. This "nascent" chlorine was presumed to be an active intermediate in the production of chlorine (C1,l from chloride ions. The study used UV light to produce an activated chlorine atom intended to recreate the observed increase in the gold dissolution rate. Although no change in the kinetic rate was observed, the reaction mechanism by which chlorine reacts with particulate gold was instead determined. Various concentrations of multivalent cationic chloride salts were added to the leach solution to demonstrate that the increased dissolution rate was due to the increased concentration of the chloride ion and ionic strength of the solution.

Jan 1, 1992

By Henrique Kahn

The Anitapolis alkaline massif in southern Brazil underlies a sub circular area of 6 km2. Bore-hole data show a concentric rock distribution, with mafic rocks in the central part and felsic rocks in the border zone. The rocks are covered by talus and weathered material, 30 m thick on average, and very inhomogeneous in composition. Phosphate mineralization associated mainly with two levels of the weathering mantle and with fresh rocks. A preliminary ore-type classification was based on distribution of apatite, feldspar, vermiculite, biotite-phiogopite, calcite, pyroxene, amphibole and analcime, determined by semiquantitative diffraction method. Technological tests performed on eluvial ore samples from three adits resulted in a subdivision of ore-types based on the difference in behavior due to mineral characteristics during mineral pr

Jan 1, 1991

By E. S. Geskin

"This paper is concerned with the construction of a formal technique for the selection of a metallurgical technology. Exergy consumption is used as the criterion of process efficiency. Different items of the exergy balance are considered and techniques for the reduction of exergy consumption are determined. The selected techniques of exergy saving enable us to identify processes which should be used at different stages of steelmaking. The combination of the selected processes enables us to suggest a technology for conversion of iron ore into steel products. The selection of this technology narrows the range of further search of metallurgical processes. The paper shows that qualitative thermodynamic analysis can be used as the first step in the design of metallurgical processes. IntroductionThe existing processes for making, shaping and treating of steel enable us to convert the available iron bearing ores into marketable steel products. However, the energy cost of metal production is much higher than thermodynamically required, while the metal properties are much lower than thermodynamically available. Increasing cost and declining availability of energy and raw meterials make the creation of new steelmaking technologies imperative. In recent years, the number of novel processes for the making, refining, and shaping of steel have been suggested and tested. Some found a practical application. However, the tested technologies make up a small portion of the physically available routes for the conversion of iron ore into a marketable product. It is also not evident that the optimal routes have been tested and that the selected technologies are the best among those tested.Although the development of new metallurgical technologies must be based on the experimental and practical information, the number of the alternative routes for the making, shaping and treating of steel, as well as the cost of examining each single route, make necessary the use of analytical techniques for the evaluation of the possible ways of process development."

Jan 1, 1988

By Byung-Su Kim

The reaction between calcium sulfate and hydrogen is of interest both as a means of regenerating calcium sulfide as a reductant of sulhr dioxide to elemental sulhr and for producing elemental sulhr from gypsum. This reaction was investigated using a thermogravimetric analysis technique in the absence and presence of nickel catalyst. The reaction temperature was varied between 973 and 1153 K, while the hydrogen partial pressures of 12.9 - 86.1 kPa were utilized. At 1073 K and a hydrogen partial pressure of 86.1 kPa, 60 % of the original calcium sulfate in the absence, and 95 % in the presence, of the nickel catalyst was converted to calcium sulfide in one hour.

Jan 1, 1999

By Alessandro Blasi, Massimo Morgana, Corradino Sposato, Pietro Garzone, Giuseppe Devincenzis

A comparison among (2-ethylhexyl)-mono (2-ethylhexyl) ester Phosphonic acid (P507), Secondary-octyl phenoxy acetic acid (CA-12) and Bis(2,4,4-trimethylpentyl) phosphinic acid (Cyanex272), in heavy rare earths separation via hydrometallurgical processes has been investigated. The separation coefficients, , were obtained and the extraction selectivity has been evaluated using a mixture of heavy rare earths from Samarium to Ytterbium. The experimental results indicated that P507 and Cyanex 272 display a greater affinity for heavier rare earths while CA12 proved to be more effective for the lighter rare earth metals.

Jan 1, 2014

By Jian Li, S. Penttilä, P. Liu, W. Zheng, C. Bibby

"The materials selection for Gen IV supercritical water reactor in-core components faces major challenges due to severe operating condition. The current Canadian pressure-tube supercritical water (SCW) concept design requires core outlet temperature of 650 °C at 25 MPa with peak cladding temperature reaching as high as 850 °C. Aside from oilier challenges, there is currently very limited data on candidate stainless steels' corrosion resistance under this operating condition. Austenite stainless steels that include 316L, 304H, AL6XN and 3 l0S that cover a wide range of Cr contents are promising candidates for either direct in core applications or as base coating materials. However, their corrosion resistance has not been tested systematically under this stringent condition. In this study, these types of stainless steels are tested, and their corrosion resistances are compared.IntroductionThe Canadian pressure-tube supercritical water (SCW) concept will operate at a core outlet temperature of 650 °C at a pressure of 25 MPa, with potential peak cladding temperature reaching as high as 850 °C. High-temperature corrosion resistance is one of the key design requirements for fuel cladding components. As summarized by Allen [1 ], most testing to date has been carried out at temperatures below 730 °C. To date, SCW corrosion data above 600 °C is very limited. Even at relatively low temperature exposure to SCW (e.g. 500 °C), F/M steels develop a thick oxide layer rapidly, while some austenitic stainless steels develop thinner surface oxide. Ni based alloys appear to form very thin surface oxide, however pitting was observed in the vicinity of intermetallic precipitates [2-5]. Dissolution of major alloying components from all of these alloys could also pose significant problems for downstream piping [6]. Kaneda et al. [7] suggested some modified stainless steels provide better SCW general corrosion resistance, with no sign of SCC under the slow-strain rate test.Cho [8] suggested that as the Cr content increase, general corrosion resistance improved at 510 °C and 25 MPa. However, similar to Cho's work, most of the SCW corrosion resistance assessments were based on weight change measurement. This can be unreliable due to potential exfoliation of thick oxide film. Besides, there have been no systematic SCW corrosion resistance tests for candidate stainless steels under higher temperatures. SCW corrosion rate increase dramatically for alloys tested at 600 °C [1]. It is also important to understand the role of major alloying elements under this stringent operating condition, not only for fuel cladding components' materials selection, but also for coating materials development."

Jan 1, 2013

By J. K. Brimacombe

"Nearly all the easy things have been investigated in injection metallurgy. Water models have been used exhaustively to study mixing, gas distribution and flow in submerged jets. Mathematical models have been developed with their restrictive boundary conditions to quantify submerged gas jet behavior. While being valuable tools to our understanding of injection metallurgy, there is an obliqueness to their application. What we need now are measurements and modelling on the actual systems, hot and unfriendly, where gas meets liquid at temperatures above l000°C. This is where the challenge lies.AN APPRECIATONThere are those who follow the trail and there are those few who blaze new trails in search of novel concepts and processes. With his restless, inventive mind, Howard Womer is a trail blazer without doubt. Decades ago, he was a pioneer in the pursuit of continuous steelmaking with the WORCRA Process and, today, he is developing new processes for the treatment of waste. He is not only an inventor but has been a professor at the University of Melbourne and was the first Director of Research at BHP. He has influenced the lives of many people, including myself; with his achievements and humanity. Therefore it is most fitting that this symposium should be held in honour of Howard Womer, a luminary in the metallurgical world for over half a century.BACKGROUNDGas injection has been an integral part of pyrometallurgical processes since the early days of Bessemer, then of Pierce and Smith. Today, of course, one cannot imagine pyrometallurgical processes without submerged gas injection to effect reactions for metal extraction and refining, to provide mixing and to inject solids into molten metal, slag or matte. Spurred on by new developments like tonnage oxygen and argon production, the Savard-Lee concentric tuyere and porous plugs, new steelmaking processes have emerged; and now solids injection is changing copper extraction processes. The ingenuity of the extractive metallurgists who drove these developments is inspiring for they have applied gas injection to transform pyrometallurgical processes. Humankind has been the beneficiary.' Today these processes are safer, more efficient, cost effective, less energy intensive and more environmentally friendly."

Jan 1, 1996