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By Krishna Kumar

"Growth of electronics waste (e-waste) and lack of appropriate disposal mechanism are the great concern for developing countries like India. The domestic generation of e-waste in India is rapidly growing with the development. The imported substance is also substantially contributing to the e-waste inventory. Recycling of e-waste is mainly carried out in unorganized units in India. The primitive recycling technique used by the unorganized sector is a great threat to the environment and the health of the operators involved in these profession. Therefore, improvement of technology used by these units towards a cost effective, environmental friendly alternative could be the solution to the present crisis. Few initiatives of recycling have, however, come up in recent years in organized units. The precious metals are still recycled in the developed countries. This report discusses the inventory, technology status, legal legislative and existing practices of e-waste management in India.1. INTRODUCTIONInnovation, research and development in the field of electronics and information and communication technology (ICT) lead to convenient, independent human life. Consumption of electronics and hardware products has enhanced by manifold. Electronics and hardware sectors have, thus, become the fastest growing sector in the world. Faster obsolescence of these products is forcing users to replace products with an advanced technology. Life cycles of these products are few years. Discarded electronics products are, therefore, accumulating alarmingly in our society. Electronics waste (e-waste) is a crisis not only due to its volume but also for presence of its toxic ingredients, like heavy metals (e.g. lead, mercury, cadmium, hexavalent chromium) and flame retardants such as poly brominated biphenyles and poly brominated diphenyles ether. These substances create potential occupational and environmental health hazardous."

Jan 1, 2011

By E. Burgos Cruz

The behaviour of S, N and P during refining of Fe-18 wt%Cr-10 wt%Ni with calcium carbide was investigated. The effects of the initial contents of C and N in the metal phase, as well as the supply method of calcium carbide to the melt on the removal degrees of S and P were evaluated. Heats were carried out at 1873K, in MgO crucibles, using a laboratory induction furnace. It was observed that simultaneously with S and P, N and O have also participated in the reactions. It seems that, in fact, O governs the behaviour of the other elements dissolved in the melt and that N is had to the removal of P with calcium carbide. It was also noticed that high C content in the metal phase have not altered the dephosphorization and desuffirization degrees, but that the supply of calcium carbide done by injection led to a lower dephosphorization degree than the one obtained by dumping it.

Jan 1, 1995

By Yuhua Pan

Generic mathematical models have been developed for simulating heat transfer in two types of slag resistance heating electric furnaces for sulphide smelting: i) six-electrode-in-line rectangular furnaces and ii) three-electrode circular furnaces. The models are based on three-dimensional steady-state heat transfer of conduction, convection and radiation. Solidification of liquid slag into solid slag by water-cooling units, for use as freeze lining of furnace walls, is also considered in the models. The developed models are capable of providing predictions with reasonable accuracy for electric furnaces on 1) temperatures in slag, matte, cooling water, freeze lining and other solid regions as well as temperatures at various fluid/solid interfaces, 2) freeze lining thickness, 3) furnace smelting rate and 4) furnace heat loss rate. These computer models are built into executable application programs that are very efficient, with execution time less than one second, and can be easily portable to most computing platforms. This paper describes, as an example, the modelling results on heat transfer in six-electrode furnaces. The major modelling results show that in six-electrode furnaces uniform electric power inputs to the electrodes likely lead to low temperature regions close to slag and matte tapping ends of the furnaces, and the power input and the formation of air gaps between freeze lining and cooling units have significant influences on the thickness of freeze lining maintained by the cooling units.

Jan 1, 2006

By T. T. Chen, J. E. Dutrizac

Noranda Inc., CEZinc presently employs a cement-stabilization (jarofix) process to stabilize its jarosite residues for direct disposal. In this process, Portland cement partly decomposes Na-jarosite to form Ca6Fe2(SC>4)3(OH)i2.nH20, ferric hydroxide and sodium sulphate which further reacts to form gypsum; approximately one-third of the Na-jarosite reacts in the current commercial product. The cured jarofix products also contain minor amounts of various Ca-Al-Fe silicate-sulphate-hydrate phases and traces of calcite. Together with gypsum and a Ca-Fe sulphate phase, these species bond the various particles together, imparting mechanical strength and reducing the permeability. Water-soluble Zn and Mg are stabilized in the Ca-Al-Fe silicate-sulphate-hydrate phases. The freshly cured products usually contain small amounts of moisture and traces of residual Portland cement, which provides additional alkalinity for the neutralization of any residual acid species. Jarofix products stored for more than six years in the laboratory, after curing, are usually dry and exhibit the same micro-textures as those of the freshly cured products. However, the stored products are depleted in the Ca6Fe2(S04)3(OH)i2.nH20 and Portland cement phases, and are enriched in gypsum and calcite which reflects the highly alkaline environment of the jarofix products. The aged products also have increased amounts of the Ca-Al-Fe silicate-sulphate-hydrate phases which have elevated Zn and Mg contents. This implies a further immobilization of residual water-soluble Zn and Mg during stora

Jan 1, 2000

By J. M. Brupbacher, D. C. Nagle

"The XD TM * approach to producing metal matrix composites employs an in-situ precipitation technique for the formation of the reinforcement directly in the matrix of interest. Key features include: thermodynamically stable reinforcement; clean particle/matrix interfaces, single-crystal reinforcement; size, chemistry, and shape control; uniform distribution; compatibility with conventional ingot techniques; and grain refinement.Using XD~ technology it is possible to simultaneously introduce a number of different reinforcements in a given matrix, thus allowing for designing the microstructure to meet a specific material need. Thus, XD1l'1 technology is a very useful technique for achieving ""designer"" or ""engineered"" microstructures. XD TM technology has been applied to a number of systems including AI, NiAI, TiAI and Cu. Materials property and processing benefits will be discussed."

Jan 1, 1988

By Roberto Parra, Roberto Parada

"A novel process for minor elements control in copper pyrometallurgical production is proposed based on a theoretical analysis and the results of an experimental program. Its application can solves operational problems related to volatile elements that determine pollutants gas emissions and the final quality of anodes. The process considers a calcination of mixtures of the dust with sulfidizing agents such as dirty copper concentrate or elemental sulfur at temperature under 800 °C. The product are a clean calcine that recovers all the Cu content on the dust and a gas stream that collect the minor elements as sulfides species. The calcine can be returned to the smelter avoiding the As increasing in the circuit and so on, the capacity for the treatment of dirty concentrates for the smelter can be higher. The possibility to apply vacuum in the calcinations step can decrease the operation temperature. The solid condensed from the gas has different options for its stabilization, with the advantage that this stream represents few mass with high As content.IntroductionThe control of undesired minor elements (IVIES) in conventional pyrometallurgical copper production is especially relevant for ore deposits associated to Andes region. The concentrates that are being produced present every time higher levels of volatiles and harmful elements: group Va (As, Sb and Bi), Pb, Zn, and Sn."

Jan 1, 2008

By Yang Cui

The partition ratios of lead and antimony between liquid copper and MgO saturated Cu2O-CaO-SiO2 flux and their removal rate by using CuCl-based flux were measured between 1423 K and 1573 K. For Cu2O-CaO-MgOsatd. system, the partition ratio of Pb was not affected by the CaO content at 1573 K, while that of Sb increased with increasing CaO content. The maximum value was 160 at the CaO content of 15.4 mass%. For Cu2O-CaO-SiO2-MgOsatd. system, two liquid phases of calcium silicate rich phase and Cu2O rich phase were observed at 1573 K. The partition ratios of Pb and Sb between calcium silicate phase and liquid copper depended on the (mass%CaO)/(mass%SiO2) ratio. When the (mass%CaO)/(mass%SiO2) ratio increased, the partition ratio of Pb decreased and that of Sb increased. For CuCl flux, the removal of Pb from liquid copper at 1473 K was possible, and a relatively low concentration could be reached. Moreover, most of lead as metal chloride vaporized from flux. For the removal of antimony from liquid copper at 1423 K, it was difficult by CuCl flux, and the removal ratio was approximately 20% for 75 minutes. However, the addition of CaO or Na2CO3 to CuCl flux was relatively effective to remove antimony, and the concentration of antimony reached a relatively low value after 15 minutes by using CuCl-CaO or CuCl-Na2CO3fluxes. Moreover, a small part of antimony as chloride vaporized from flux.

Jan 1, 2006

By Anita E. Lam

The thiosulfate leaching of gold generally requires the presence of a catalyst such as cupric tetraammine, Cu(NH3)42+, to obtain reasonable leaching rates and gold extractions. Unfortunately, this same catalyst that accelerates gold leaching also tends to accelerate thiosulfate oxidation to tetrathionate and other species. It is therefore imperative that a detailed understanding of the role of this catalyst and the factors affecting it is obtained. It is equally important for plant application that a method of assessing the catalyst be developed. In this work the role of the cupric tetraammine catalyst was studied using geochemical modeling for speciation prediction, thiosulfate leaching of gold ores, and chemical analyses of resulting leach solutions. It was found that the variables of pH, temperature, and the concentrations of ammonia, thiosulfate, and total copper all work in concert to affect the concentration of the cupric tetraammine species. It was also found that the presence of sufficient thiosulfate and cupric tetraammine was critical to the success of the leach.

Jan 1, 2003

By P. K. Jha, M. M. Mahapatra, H. K. Mohanty, Pradeep Kumar

"During friction stir welding, the tool geometries affect the weld together with the process parameters like welding speed, vertical pressure and tool rotational speed. The present investigation deals with the three dimensional computational fluid dynamics modeling of friction stir welding process considering material flow around the tool, welding speed with respect to tool geometries. Friction stir welding tools with different tool geometries were used for the experiments to achieve acceptable aluminum welds. The temperatures near the welds for each tool were experimentally observed. A 3-D computational fluid dynamics (CFD) model was developed. Temperature-dependent material properties of the aluminum alloy were used in the CFD model. Thermal analysis was carried out considering rotational speed, vertical pressure and traverse speed for the tool geometries. The numerically predicted stirring patterns and temperature profiles closely matched with the experimental ones. IntroductionThe friction stir welding (FSW) is a solid state welding process where generally the metallic materials are joined by the combined action of frictional heating and weld zone stirring by a rotating tool [1]. The heat generated in the process is much below the requirement of melting the plates; hence the FSW process is devoid of harmful effects those are observed during arc welding. The FSW process utilizes a tool which has a shoulder and a protruding pin known as the probe. The shoulder is responsible for frictional heating while the pin probe facilitates stirring of the joint material. A schematic of FSW process is shown in Fig. 1."

Jan 1, 2012

By Zbigniew Smieszek, Ryszard Chamer, Ryszard Prajsnar, Zygmunt Kurek

"Lead-containing wastes processed at the IMN’s Division in Legnica originate mainly from dry and wet dedusting installations of the technological lines for copper production. These are lead dusts and lead-zinc dusts characterised by the specific properties resulting from the chemical composition of the Polish copper concentrates. Besides lead, they contain many accompanying metals and impurities such as zinc, copper, sulfur, chlorine, potassium, sodium, and also bituminous substances. Processing of lead-containing dusts is conducted in the installations of rotary-rocking furnaces heated with gas-oxygen burners fitted with auxiliary systems for cleaning process gases and refining re-circulating dusts. The processing technology utilizes innovative process and technical solutions enabling disposal of lead-containing wastes from copper metallurgy and from non-ferrous metals industry according to the BAT recommendations and to the guidelines specified in integrated permission. In this paper, the main technological aspects of processing lead-containing dusts at the IMN’s Division in Legnica have been presented.IntroductionCrude lead is obtained in Polish lead metallurgy from various primary and secondary materials, such as Zn-Pb concentrates, lead-bearing dusts of copper metallurgy and battery scrap. In zinc smelter Miasteczko Slaskie S.A. crude lead is produced from sulfide and oxide Pb-Zn concentrates in ISP process. Orzel Bialy S.A. and Baterpol Ltd. produce crude lead in short rotary furnaces in the process of smelting products of mechanical battery scrap separation– desulfurised or not desulfurised paste and metallic fraction. KGHM Polska Miedz S.A. and IMN Divison in Legnica produce crude lead in rotary furnaces in the process of smelting of polymetallic dusts and slimes from copper production processes."

Jan 1, 2008

By Peng Peng, Ouo Cheng, Guodong Lai, Lijuan Chu, Zebiao Zhang

"The pressure acid leaching residue of zinc concentrate contains a large quantity of sulfur. The present study attempts to leach sulfur using a mixture of ammonium sulfide and water solution at 25°C. Effects of three leaching variables: ammonium sulfide concentration, leaching time, liquid/solid ratio on the sulfur leaching rate were investigated. The process conditions were optimized using response surface methodology based on the central composite design. From the analysis of variance (ANOVA), the significant factors on response were identified. The optimum conditions for leaching elemental sulfur from pressure acid leaching residue of zinc concentrate were obtained using an ammonium sulfide concentration of 2.5 mol/L, leaching liquid-solid ratio of 6.5:1 and leaching time of 7 min. Under the optimum experimental conditions, a maximum of 98.50% of total sulfur was extracted. The experimental results obtained agreed satisfactorily with the model predictions, with a correlation coefficient (R2) of 0.99.IntroductionSulfur is widely used in agriculture, medicine, rubber, building materials, gunpowder, wine and sugar, and other fields [1]. Currently the world sulfur production is 40Mt, out of which more than 90% is recovered from industrial processes, and 10% is natural [2], This highlights the importance of sulfur recovery. As the pressure leaching technologies [3] continue to mature and are increasingly applied to refining, a large quantity of high-sulfur residue is produced [4-5]. It is desirable to recover sulfur from this residue, so that it is economically advantageous, and reduces environmental pollution [6]."

Jan 1, 2012

By Leandro Voisin

A new pyrometallurgical treatment alternative is proposed for cleaning complex copper matte with high content of impurities in the copper smelting process, thus, in a suitable furnace, a given amount of pig iron will be added to the liquid complex matte with a matte grade between 65 and 75 % Cu under reducing condition and will produce three liquid phases of matte, copper-rich alloy and iron-rich alloy. Hence, in this study, firstly, a mass balance calculation was made on the basis of the reported data for the distribution ratios of the components among the three phases to define the optimum condition where most of the arsenic can be fixed in the less valuable liquid iron-rich alloy. By taking advantage of the high concentration of arsenic in the iron-rich alloy, the small volume alloy may be disposed in a yard, while the precious elements may be recovered effectively in the liquid copper-rich alloy and/or in the liquid matte. Secondly, laboratory-scale experiments were conducted to apply the proposed process to the matte produced from the slag-cleaning electrical furnace and the Teniente Converter of the Codelco-Norte smelter. The obtained results indicate that the proposed process for cleaning complex matte is promising.

Jan 1, 2006

By Bruce W. Downing

MagPower has developed methods to control the detrimental formation of hydrogen that occurs in electrochemical reactions in numerous commercial applications such as the Magnesium-Air Fuel Cell, electrowinning, zinc alkaline batteries, hydrogen embrittlement, waste water/ metal recycling and coolants. The company?s approach to an alternative energy source is the development of an environmentally friendly non-toxic alternative power source that generates electricity through a combination of magnesium, oxygen and a saltwater electrolyte with MagPower?s patent pending hydrogen inhibitors. The magnesium-air technology has never reached the commercial stage due to its limiting power output caused by hydrogen generation. MagPowerhas solved this problem and has patents pending on its intellectual property; the Hydrogen Inhibitors and has developed several consumer power units for a variety of applications through licensing agreements. The company has also shown that the inhibitors have an impact on zinc electrowinning through laboratory test work where current efficiency was improved. This will significantly reduce power consumption and increase the efficiency of the electrowinning process, as well as reduce the potential acid mist hazards associated with electrowinning.

Jan 1, 2003

By K. B. Dotson

A common international safety and health management system was developed. Analysis of selected major safety and health management systems from around the world was conducted. Functional elements of selected systems were grouped to identify common elements and key differences. Common elements were subjected to qualitative judgments of equivalency and then reconciled. With few exceptions, differing elements were revised to achieve cultural neutrality. The resulting 98 system elements were organized according to the NOSA numbering and title scheme. System summaries were produced in Spanish and English. A pre-implementation self-assessment evaluated conformance in three distinct cultures. The consensus 98 element system was internally named the BHP Copper Five Star Safety System Performance Management Guidelines. Development of a common system within an organization with international operations can enhance the ability of the staff function to share resources, programs and subsystem improvements and thereby increasingly protect workers. Common systems can increase the level of management support by demonstrating increased compatibility of the safety and health management function with traditional business objectives. Safety professionals, industrial and occupational hygienists, business managers and the safety and health of workers will benefit from further development and articulation of common systems for safety and health management.

Jan 1, 1999

Environmental and public concerns and the banned use of cyanide for the recovery of gold in some parts of the world have heightened the search for an alternative lixiviant to cyanide. Thiosulfate appears to be the most promising alternative to cyanide due to thiosulfate being non-toxic, relatively cheap compared to cyanide and generally gold recoveries are similar to those of cyanide. The most widely researched thiosulfate process is one where copper ions and ammonia are added to the solution. This paper reviews the leaching of gold in thiosulfate solutions and the contributions of the research at Monash University to the understanding of the gold oxidation reaction in thiosulfate solutions, the solution chemistry when copper ions, ammonia and oxygen are present, the influence of the changing solution chemistry on the gold leach kinetics, and the application of thiosulfate in the leaching of gold from ores. It is clearly shown that the gold oxidation rate is hindered in thiosulfate solutions. In the presence of copper ions the gold oxidation rate though is significantly enhanced and thus is why copper(II) is more effective than other oxidants in the thiosulfate leach system. The copper-ammonia-thiosulfate leach solution chemistry is shown to be very complex, especially in the presence of oxygen as the rate of thiosulfate oxidation increases and the majority of the copper ions are not maintained in the copper(II) oxidation state. The thiosulfate oxidation rate must also be maintained low as an intermediate thiosulfate oxidation product hinders gold leaching. In optimising the recovery of gold from ores with copper-ammonia-thiosulfate leach solutions it is important to evaluate and minimise any negative effect an ore may have on the leach solution chemistry and hence gold leaching.

Jan 1, 2003

By C. M. Acuna

Scarcity of high grade copper low impurity content ores is a reality and processing of low grade dirty concentrates is a need. In spite of this fact, innovative strategies have to be looked at to comply with day to day more stringent environmental regulations. From this perspective the production of matte grades over 70% in copper presents several merits, but it must be contrasted with the fractional distribution of impurities reporting to the condensed phases. Converting of white metal high in arsenic content results in moderate fraction of arsenic to gas, but high deportment to blister. Therefore, production of anode copper, as required by the electrolytic refinery, may result in several operational difficulties. Furthermore, by recycling the flue dust and slag produced in the smelting-fire refining cycle, the arsenic content in the feed to smelting increases and so does in the resulting anode copper. The Teniente Converter, as a smelting unity, has probed suitable for production of high matte grade near white metal composition but regarding distribution behaviour of impurities there is lack of reliable data, specially when processing concentrates over 1% in arsenic content. In the new scenario, i.e. low grade copper high arsenic content concentrates, to fully asses the merits of this technology the effect of matte grade, secondary materials recycling and arsenic in feed upon the distribution coefficient of arsenic between slag and matte, mainly, must be evaluated both from a theoretical approach and by use of industrial data. Based on available data correlations of distribution coefficient, matte grade and matte/slag ratios with arsenic in feed and copper content in slag are worked out. Based on these results suggestions as to matte grades facilitating to deal more efficiently with the handling of smelting byproducts are proposed.

Jan 1, 2006

By W. Gong

Their outstanding thermal stability and high energy product make Sm(Co,Fe,Cu,Zr),-type alloys attractive for advanced applications. The near net-shape production of Sm(Co,Fe,Cu,Zr), bonded magnets make them potentially superior to any magnets made by sintering. Although pioneering work done by Shimoda et al. and other investigators provide insights on the proper compositions and process control of this alloy system, additional work is still necessary to improve our understanding of alloy behavior at various processing stages and to increase the production yield during powder processing. In this paper we report on the development of anisotropic Sm(Co,Fe,Cu,Zr), alloy powders for the bonded magnet application. Our focus is on the development of a moderate coercivity powder requiring a relatively low magnetizing field to charge the magnets to their optimum Br, Hci and BHmax. The magnetic properties are related to the evolution of the microstructure at various processing stages and the average particle size and size distribution of powders.

Jan 1, 1997

By S. H. Castro

The El Teniente molybdenite plant (Chile), with a nominal capacity of 3,200 tpd of bulk Cu-Mo concentrate, produced approximately 3,385 metric tonnes of Mo during 1998 by using the phosphate Nokes process (LR-744 reagent). This is the only Chilean moly plant which traditionally has depressed copper and iron sulfides with LR 744 reagent, which is a hydrolysis product of P2S5 and NaOH. El Teniente's ore Mo grade is 0.02%Mo and is concentrated to 0.45%-0.50% Mo in bulk Cu-Mo flotation. Subsequently, molybdenite is floated by selective flotation to depress Cu and Fe sulfides, such as chalcopyrite, bornite, digenite and pyrite, to produce typically a 49%-50%Mo molybdenite concentrate. An optimisation program during the last two years was undertaken to improve molybdenite recoveries. Current molybdenite plant technology at El Teniente and use of phosphate Nokes in the process process is reported. Use of phosphate Nokes reagent has increased average Mo recovery from 70.5% in 1977 to a mean 74.7% for the first 4 months of 1999. The global Mo recovery, including bulk flotation, incresed from 42.3% in 1997 to 46.8% in 1998, with a projection of 55.5% for 1999. Mo production per year has increased from 3,181 tons in 1997 to 3,385 tons in 1998 and a projected 4,000 tons for 1999.

Jan 1, 1999

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 Suk J. Im, I. S. Min, Daesoo Kim

UFP are defined by atoms or their clusters having diameter in the range of l0Å-0.l.um. Due to a ratio of very large surface area to volume, they have peculiar properties such as extra high surface energy. Recently UFP deposition technique may find its new applications to various areas such as conductive/resistive film formation. In this method, gas flow with UFP jet through the nozzle which is considered to be a free molecular flow is maintained at a very high speed (~100m/s). Using this technique, mixture film of Fe and Ni, and Ag/ Ag-Alloy etc. were obtained, and their mechanical and electro-magnetic properties were determined. The experimental results are pending. The test results and discussion will be presented in the main paper.

Jan 1, 1988