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By Zhang Huaiwei, Shi Xiaoyan, Li Xinlin, Sun Fei, Hong Xin

"The control of the slag properties has become very essential in improving the separation between the slag and the matte in the copper slag cleaning process. The goal of the present work is to characterize the copper converting slag through chemical analysis (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with energy dispersive spectroscopy detection (EDS) and thermal analysis (DSC). The majority of the identified elements were Fe, Cu, Si and 0. The XRD has presented compounds such as Fe2Si04, Si02, CuFe204, Fe304, and Cu. The main existence of copper element was the metallic copper due to the entrainment loss. Slight amounts of copper were existed as the CuFe204 in the slag. The density, viscosity, electric conductivity and the thermodynamic property of the molten copper converting slag were also investigated in the study.IntroductionCopper slag, which is produced during pyrometallurgical production of copper from ores, contains materials like iron, alumina, calcium oxide, silica etc. For every tonne of metal production about 2.2 ton of slag is generated [l]. The slags of copper converting process contain about 5% of copper and about 20% magnetite. The copper are present in the slags either as physically entrapped or in chemically dissolved [2-3]. The traditional slag cleaning method is electric furnace process including two steps, intensive slag reduction and quiet sedimentation. Although the process is suitable for the various copper slags, it is also with the higher energy consumption [ 4-7]. The slag characterization studies are the fundamental step in the definition of an appropriate recycling process for saving the energy consumption."

Jan 1, 2013

By Manuel Alvarado, David Nemir, Jan Beck

"Thermoelectric generation using special N-doped and P-doped semiconductors is well known as a means for direct heat energy to electrical energy conversion without the need for moving parts. The technology is used today in niche markets for low level electricity production and has been proposed as a scalable means for capturing large scale energy from waste heat streams. The choice of geometry of the thermoelements and conductors is critical to the successful implementation of a waste heat recovery system in order to manage losses due to Joule heating and diffusive heat flows. This paper describes a simulation study to define the performance impact of different aspect ratios for the active thermoelements and the electrical interconnect. The use of a finite element model that incorporates the intercoupled heat and electrical energy flows highlights some of the issues impacting scalability.IntroductionThermoelectric phenomena arise out of the intercoupled electrical and thermal currents in a material. A two-element thermoelectric generator is depicted in Figure 1. It is constructed by connecting an N-type thermoelement and a P-type thermoelement in electrical series, with both elements in thermal parallel between a heat source and a heat sink. The electrical series connection is made by attaching conductors as shown. Ideally, these series connection elements will be both good thermal conductors and good electrical conductors.The two element generator in Figure 1 is disposed between two thermal reservoirs: the heat source, which furnishes heat energy; and the heat sink, which absorbs heat energy. Heat energy flux Q, flows from the heat source to the heat sink, driven by the temperature difference between the source and the sink. As depicted in Figure 1, when a resistive load, R, is attached, electrical current, I, may be extracted from the thermoelectric generator and furnished to the load. The N-type and P-type thermoelements, are the active portions that do the actual conversion of heat energy to electrical energy. Although thermoelements may be built using conductors such as bismuth and antimony, higher efficiency thermoelectrics are built using heavily doped semiconductors. Thermoelectric devices are generally formed by connecting many pairs (couples) of N and P type thermoelements in electrical series and in thermal parallel. A commercially available module having 127 couples (254 elements) is shown in Figure 2."

Jan 1, 2011

By M. Save, N. Menad

"This paper gives the overview of different alternatives to recycle the following wastes: slag, dusts, wastes of electric and electronic equipment (WEEE) and auto shredder residues (ASR). Based on modified Bogue calculations, steelmaking slags were combined in order to produce a belite-rich clinker activated with sulphoaluminate. The EAF dusts containing significant amount of metals can be recycled in different ways: The carbothermal treatment and INTECT process are reported. The results obtained from the model of Auto Shredder Residue injection into blast furnace show that ASR can be used as reducing agent in the BF process if certain conditions are met. The particle size of this material must be controlled to ensure optimal gasification of the material in raceway. The non-ferrous contents may affect the pig iron quality, which is difficult to rectify at a later point. It seems the pyrolysis is the most attractive process to handle ASR. The BRGM flow sheet of WEEE treatment is also reported.I. Introduction The activities of human been may generate wastes and by their accumulation during several years, these wastes may have an impact on the environment and on the human health. These wastes can be generated in the forms of solid, liquid and gas. A variety of industrial wastes can be recycled for use as products. There are three ways in which industrial waste recycling occurs: at the facility itself (on-site recycling), at commercial facilities that gather waste streams from several companies (off-site recycling), and at a company that uses as inputs in its production process the waste products of another company. The industries producing iron and steel may generate different solid wastes which are classified in three main categories: 1. Ferrous material (mainly dusts and sludges from gas cleaning), 2. Slags (these by-products are generated from different process stages), 3. Others by-products (including refractories and material generated from engineering activities). According to this review, the most quantity of the metallurgical wastes is deposed. Currently, the public opinion opposes the creation of new sites. This leads to the growth of the waste disposal costs. Such situation reduces the enterprise competitiveness and decreases their market share on regional and/or national and/or world scales. In these conditions, the economical activities can be decreased leading probably to social problems. The problem of wastes and/or by-products can be treated on three levels:"

Jan 1, 2008

By Robert T. Oxnard

"EXECUTIVE SUMMARYThe history of Refractory Recycling indicates there was little recycling until the 1950s. Energy incentives were the primary reason for the beginnings of a recycling effort by the refractory brick manufacturers. Quality benefits quickly became evident and fewer rejects were the result. Today, economic factors including higher valued raw materials and increased competition are the driving forces of refractory recycling.There are some success stories in refractory recycling but we have a long way to go. Few incentives, quality concerns, relatively cheap energy, comparatively lax government regulations, inexpensive landfills and inexpensive substitutes make recycling a difficult choice for many companies. Marketing advantages such as ISO 14000, eliminating multiple audits and reduced liability exposure can tip the scales toward recycling viability. Increasingly, the ideological philosophy of a company, a desire to minimize environmental impact and develop favorable public and other interested party perceptions can drive recycling and waste minimization efforts.Recycled materials can be more trouble ""up front"" and harder to ""manage"" due to their suspect quality. However, due to their nearly inexhaustible supply and the fact that once developed, they constantly contribute to the bottom line, they are certain to be the materials of the future. Waste refractory materials will likely see the same bright future as the steel scrap yards and slag piles of yesterday. In hindsight, we will realize that now was the perfect time to prepare and plan for the bright future of refractory recycling."

Jan 1, 2000

By Rong Yang, Qijie Zhai, Wenbin Xia, Changjiang Song

"Tills paper focus on the influence of carbon content and cooling rate on the microstructure and phase formation of Fe-Mn-C alloys under near-rapid solidification. When manganese content is about 11wt.%, more s-martensite can be obtained with cooling rate increasing when carbon content is 0.14wt.%, the formed phase changed from a phase to y phase when 0.74wt.% carbon is added to the samples, and when carbon content up to 2.1wt.%, carbide can be obtained in the sample. A host of stacking fault, which attributes to the strain-induced martensite, can be observed in the sample. The microhardness increased with cooling rate increasing, and under the same cooling rate, the microhardness of samples with 0.14wt.% carbon is highest.IntroductionTo obtain high performance materials is eternal pursuit of material science research. Material scientists have explored many new ways to obtain high performance materials from long time ago. Rapid solidification is one of most popular ways to produce advanced materials by obtaining metastable phases, because it is widely known that the solidification of metals in metastable phases gives access to a whole range of materials with novel properties [1]. Furthermore, nowadays metastable materials have been extensively used in many fields, for example, many of our modem high performance materials such as steel products or aluminum alloys for aeronautical applications are in the form of metastable rather than stable phases [1]."

Jan 1, 2012

By M. Cassir

"The unique properties of molten carbonates offer a large scope of applications in the field of energy. In effect, these molten salts are in the center of chemical and electrochemical reactions involving carbon and carbonaceous species, carbon dioxide and carbon monoxide, significant for energy generation or even for the production of fuels. Moreover, such media have also an oxidative character; they dissolve molecular oxygen and oxygen reduced species, O 2-, O22- and hypothetically o-, which may have an important role in waste treatments, homogeneous catalysis and synthesis of oxides. In this presentation, an overview will be given on the principal physicochemical properties of molten carbonates, before focusing on their main known application, the molten carbonate fuel cell (MCFC). Progress in other new fuel cells applications will also be analyzed, such as direct carbon fuel cell (DCFC), hybrid carbon fuel cell (HDCFC) and composite high-temperature fuel cells combining the features of MCFC and solid oxide fuel cell (SOFC). Afterwards, membranes for the separation and capture of C02 will be reviewed. Finally, other topics, as the oxidative coupling of methane in molten carbonates, will be briefly mentioned.IntroductionIn the thirty past years, the molten carbonate science and advances have been mainly dedicated to the understanding and optimization of the molten carbonate fuel cell (MCFC), which is still a major issue in the heart of a new vision of energy development. More recently, new topics related to other kinds of fuel cells (DCFC, composite SOFC/MCFC systems) and C02 capture have emerged and are concentrating important research and technological efforts. Moreover, new fields of implementation, related to molten carbonates, are also present: geology, glasses, production of nanocarbon particles etc. Considering other areas where this molten phase plays a major role, such as catalysis, waste destruction, surface treatment, it can be confirmed that the field of molten carbonates is very rich and offers many opportunities for fundamental science and competitive applications. Whatever their specific application, molten carbonates activity is associated to more efficient energy systems with low production of C02 and, in a prospective sense, to non-polluting energy using the value of C02. A recent event, the International Workshop on Molten Carbonates & Related Topics, IWMC201 I, held in Paris in 2011 , have put in evidence the importance to improve and exploit this investigation and technological domain."

Jan 1, 2012

By V. Montenegro

Smelting of copper concentrates in Teniente Converter produces highly oxidized slag, containing from 4 to 10 % Cu and from 15 to 25 % of Fe304. Copper recovery requires magnetite reduction at a level of 5%, determining the degree of cuprous oxide co-reduction and the liberation of copper matte inclusions. The rate of slag reduction is controlled by the mass transfer to the reaction interface. Slag stirring affects the rate of reduction and enhances coalescence of mechanically entrained copper matte inclusions. Slag reduction and sedimentation in the AC electric furnace is a commonly used method of slag cleaning. Utilization of DC electric furnace creates beneficial conditions introducing slag electrolysis additionally to chemical reductions with carbon of coke and electrodes. Application of external magnetic field, interacting with a direct current in an electric furnace, induces magnetohydrodynamic phenomena, such as intensive stirring and electromagnetic buoyancy force acting on inclusions. Laboratory scale research in simulated DC electric furnace with a superimposed magnetic field showed a significant acceleration of the rate of slag reduction and copper removal. Continuous measurement of gas flow and composition allowed for determination of the reduction rate along the time. Application of external magnetic field in the reduction of the industrial slag in a crucible simulated DC electric furnace results such as the increase of the reduction rate from 2 to 3 times, compared with the identical conditions in the AC electric furnace. Interaction of non-homogeneous electric field with crossed permanent magnetic field induces vigorous slag stirring, enhance mass transfer and accelerate the rate of the slag reduction. Additional participations of the slag electrolysis in the magnetite and cuprous oxide reduction as well as the acceleration of the settling of the inclusions by the electromagnetic buoyancy force affect the slag cleaning intensification.

Jan 1, 2003

By Hiroaki Kawamura, Takeshi Yoshikawa, Kazuki Morita, Yutaka Yanaba

"To develop an alternative metallurgical process for phosphorus removal in the production of solar-grade silicon (SOG-Si), slag treatment of metallurgical-grade silicon (MG-Si) was conducted, followed by acid leaching. Phosphorus-doped silicon alloy or MG-Si containing certain amounts of phosphorus and calcium was reacted at 1723 K and 1773 K with CaO--CaF2 of several compositions. Phosphorus removal from the molten silicon into the slag phase was confirmed by reduction to phosphide ions, P3-, and phosphate ions, P3-. These ions were separately determined using a wet chemical analysis method developed by ourselves. The highest phosphorus distribution ratio obtained was 2. 7 after reaction for 18 h with 17.5 mass% CaO--CaF2 slag. We then conducted acid leaching of the silicon and achieved removal of a large fraction (over 90 % ) of the phosphorus, which was much higher than that obtained by ordinary oxidizing slag treatment.IntroductionIn recent years, the production of solar cells has been increasing rapidly. Because of this, the demand for solar-grade silicon (SOG-Si) has also been growing rapidly. The development of lower-cost mass production processes is therefore needed to provide silicon feedstock. Phosphorus is one of the impurities in metallurgical-grade silicon (MG-Si). Because of its large segregation coefficient (kp = 0.35) [l ], it is difficult to remove phosphorus using a solidification refining process. Vacuum melting is considered to be a promising method for removing phosphorous from MG-Si [2], but the issues of high cost and large energy consumption have still to be resolved.Slag treatment is often used to remove impurity elements by oxidizing reactions during general oxidation refining processes. For example, phosphorus in molten steel is removed into a slag phase as phosphate ions, PO4 3-l-, by the following reaction:"

Jan 1, 2013

By Biswadeep Saha, Meenakshisundaram Ramanathan, Chai Ren, Sivaraman Guruswamy

"Fe-Ga alloys have a large low-field magnetostriction and these alloys are attractive candidates in energy conversion and harvesting applications. Small additions of W also increase the magnetostriction of Fe. In this paper changes in magnetostriction by W substitution for Ga in various Fe-x at.% Ga alloys are presented. Fe-Ga-W single crystals were grown using vertical Bridgman Growth technique. [001]-orientated single crystal samples were prepared with faces within 1 degree off <100> orientation. The samples were annealed at 1150 °C in the alpha-phase region and water quenched. The magnetostriction coefficient (3/2)A-100 measurements were made on these Fe-Ga-W single crystals. The result on the effects of W substitution and annealing on the magnetostrictive behavior of these alloys are discussed.*Support of this work by NSF-DMR under the award DMR-0854166 is gratefully acknowledged.IntroductionMagnetostrictive materials changes their dimension exhibit reversible strains and changes in elastic properties in the presence of an applied magnetic field or the reciprocal effect of changes in the magnetic properties with the application of stress [IJ and are very important in sensor, actuator device, linear motor, magnetomechanical devices, microelectro- mechanical devices, active vibration dampening devices application areas. The discovery of an order of magnitude enhancement in the magnetostriction of Fe with Ga addition coupled with low saturation magnetic fields, and excellent mechanical properties opened up the possibility of obtaining larger magnetostriction values in other low-cost ductile a-Fe phase based alloys with alloying additives that are less expensive than rareearths such as Tb and Dy [2·4l_ The magnetostriction values observed in Fe-Ga single crystals are sensitive to thermal history and composition. The formation of second short range ordering phases and local defects inside crystal structure can also cause a dramatic change to this alloy's magnetostriction behavior [5-9l_"

Jan 1, 2012

By V. Montenegro

Smelting of copper concentrates in Teniente Converter produces highly oxidized slag, containing from 4 to 10 % Cu and from 15 to 25 % of Fe304. Copper recovery requires magnetite reduction at a level of 5%, determining the degree of cuprous oxide co-reduction and the liberation of copper matte inclusions. The rate of slag reduction is controlled by the mass transfer to the reaction interface. Slag stirring affects the rate of reduction and enhances coalescence of mechanically entrained copper matte inclusions. Slag reduction and sedimentation in the AC electric furnace is a commonly used method of slag cleaning. Utilization of DC electric furnace creates beneficial conditions introducing slag electrolysis additionally to chemical reductions with carbon of coke and electrodes. Application of external magnetic field, interacting with a direct current in an electric furnace, induces magnetohydrodynamic phenomena, such as intensive stirring and electromagnetic buoyancy force acting on inclusions. Laboratory scale research in simulated DC electric furnace with a superimposed magnetic field showed a significant acceleration of the rate of slag reduction and copper removal. Continuous measurement of gas flow and composition allowed for determination of the reduction rate along the time. Application of external magnetic field in the reduction of the industrial slag in a crucible simulated DC electric furnace results such as the increase of the reduction rate from 2 to 3 times, compared with the identical conditions in the AC electric furnace. Interaction of non- homogeneous electric field with crossed permanent magnetic field induces vigorous slag stirring, enhance mass transfer and accelerate the rate of the slag reduction. Additional participations of the slag electrolysis in the magnetite and cuprous oxide reduction as well as the acceleration of the settling of the inclusions by the electromagnetic buoyancy force affect the slag cleaning intensification.

Jan 1, 2003

By Nathaniel R. Quick

"Nd: YAG, KrF excimer, and Cu-vapor lasers are used in air to synthesize conductors and semiconductors as a second phase in silicon carbide and aluminum nitride. Conductor resistivities as low as 104 O-cm are formed in these substrates; the resistivities for the untreated substrates range from 10 11to 1014 O-cm. The silicon carbide conversion is relatively independent of wavelength while the aluminum nitride conversion shows a dependence on wavelength over the range 248 nm to 1064 nm. Silicon carbide conductors, evaluated over the range 15 K to greater than 300 K, exhibit metal like conductivity; resistivity increases with temperature. Silicon, carbon, and oxygen are identified as the principal chemical species associated with the conductor in SiC substrates while aluminum, nitrogen, and oxygen are identified as the principal chemical species associated with the conductor in aluminum nitride substrates. The silicon carbide system, which has the less complex phase diagram, is evaluated in more depth to explain the synthesis mechanism. Oxygen was principally on the surface and increasing SiC conductivity is associated with decreasing spacing between 5 µm, or less, diameter carbon globules. This technology is proposed as a replacement for metallization in electronic packages, sensors and devices. INTRODUCTIONCeramics are commonly used for multichip module, hybrid and multilayer electronic packaging; semiconductor device and sensor applications because of the insulating, conducting, semiconducting, or superconducting properties that these materials possess (1,2) The majority of ceramics, however, have not been known to exhibit conductive or semi conductive properties when exposed to rapid thermal heat processing. A ceramic and process which through selective conversion can combine two or more of these electrical properties to eliminate the need for metallization is of interest to both the commercial and military sectors."

Jan 1, 1994

By Maura Malone, Neil Gao, Daniel Liu

"Corrosion is the primary failure mode for aluminum cathode sheets used in Teck's Trail Operations electrolytic zinc plant. It was observed that the corrosion performance of Al cathodes from different suppliers varied considerably. This suggests that the material properties of Al cathodes have a strong influence on corrosion resistance. In the current study, various types of Al alloys, including 1050, 1060, 1070, HIS and 1090, were characterized through chemical analysis, corrosion testing, mechanical testing and metallography. The results are discussed with a focus on the effects of impurity elements and second phase particles on corrosion resistance. The findings were used to improve the Al cathode sheet specification and to develop a standardized screening procedure which details qualification steps for comprehensive evaluation prior to a plant trial.IntroductionAluminum (Al) cathode replacement is a major operating expense at Teck's Trail Operations zinc electrolytic plant. Currently, approximately 0.5% of daily stripped Al cathodes are removed from service because of failures caused mainly by corrosion. Edge corrosion and acid (solution) line corrosion are the most severe types of corrosion, resulting in more than 50% of cathode failures.Corrosion of Al cathodes has been intensively investigated for over two decades and the origins and mechanisms of Al cathode corrosion are well understood [1-4]. Halide anions contained in the electrolyte are the primary culprits for the corrosion and sticking problems of Al cathodes. Both fluoride (F') and chloride (Cl"") result in localized passivity breakdown on the surface of the Al cathode, causing pitting corrosion. Bouarzaiga investigated the corrosion of Al cathode samples partially immersed in electrolyte and found that the formation of Ch at the electrolyte/air interface was the primary contributor to solution line corrosion [2]. Because of the significant impact of F"" and Cl"" on Al cathode corrosion, it is imperative to maintain these concentrations as low as possible in the electrolyte."

Jan 1, 2012

By Sergio Bustos

Covellite resulting from an original 0.5 % Cu(tot) chalcocite ore has been leached in columns at different temperatures, in the lower range of 10 - 20 °C, under acid - ferric bacterial leaching conditions. Dissolution of copper from covellite depends on the rate and extent of sulphide oxidation by ferric ion. While it is recognised that the dissolution of sulphide minerals is electrochemical in nature, an apparent chemically controlled dissolution pattern was measured with activation energy of 78.09 kJ/mol (18.66 kcal/mol). Ferric iron is the main oxidant and its production and availability will depend on the bacterial activity developed in the system. This activity is characterised by the population size and by the specific oxidation rate of the bacteria. Bacterial growth was followed directly by the number of bacteria appearing in the column effluent solutions and indirectly by the generation of ferric iron or by the total oxidation observed in the columns. These results have been interpreted by using the heap oxidative capacity parameter, which indicates an equivalent ferric production of about 0.07 - 0.15 kg Fe +3/t/day at 20°C. Although bacterial activity decreases to about 0.03 kg Fe +3/t/day with decreasing temperature, a significant bacterial oxidation is still observed at 10 °C. However, extended lag times are observed, which delay the start of bacterial growth to times concurring with covellite leaching. Under these conditions, bacterial activity is displayed through a population controlled by the rate at which- ferrous iron is released from the reducing covellite surface. These results suggest the potential benefit of including some kind of inoculation when operating at lower temperatures. Also, heat loss control and/or heat addition to the heaps should be considered during process design and operation of ferric bacterial heap leaching of secondary copper sulphide ores at temperatures lower than 20°C.

Jan 1, 1999

By Cristiän Vargas, Jaime Simpson, Gerardo Cifuentes

"This paper presents a new process for the precipitation of Sb and Bi present in copper refinery electrolytes in the presence of Pb02 (Chilean Patent No. 45,037). To establish the conditions under which the precipitating compounds form, it was necessary to evaluate the amount of PbCh consumed, antimony extraction efficiency, precipitate stability, reaction kinetics, diffraction analysis and X-ray fluorescence, separation of size, plus observation of the precipitates in the electron microscope. Preliminary tests were carried with synthetic copper refinery electrolyte, and then the final testing was done with electrolytes from Chilean refineries. This process provides a real alternative for the treatment of copper refinery electrolytes for the control of Sb and Bi in solution; it is very simple to operate and is low cost compared with competing processes.Introduction.A high quality copper cathode implies a cathode free of impurities. The electrorefining process seeks to eliminate these impurities from the copper anode (99.5% purity) by its dissolution in an acid electrolyte using chemical and electrochemical reactions. As a result of this process, a cathode (99.99% purity) is obtained. If the concentration of impurities in the electrolyte, from the dissolved anodes, begins to increase; particularly if the antimony concentration in the electrolyte increases up 500 ppm, the formation of floating slimes which are a major cause of contamination of the cathode is favoured. The most important impurities from the point of view of their effect on the quality of the cathode copper, are Ag, As, Sb, Bi, Pb, Se and Te. Silver is necessary for the control of Se and Te. To control all of these impurities, it is necessary to establish different methods or parameters of control in copper electrorefining. These parameters are anode composition, additives, purification of the electrolyte, current density, acidity, etc."

Jan 1, 2012

By T. Gunawansa, T. L. Alford, Zhao Zhao, A. R. Lanz, N. David Theodore

Many sustainability issues arise during the manufacturing processes that are currently used for solar cells. Solar energy is a renewable energy source that is independent of the earth’s resources, and it is therefore important for the development of more sustainable technologies. Microwave annealing (MW) has been proposed as a technically feasible fabrication scheme for large area silicon solar cells. Apart from that, microwave annealing has been demonstrated to be a promising alternative for repairing damage and electrically activating dopants in ion-implanted semiconductors for integrated circuit manufacturing. A microwave oven is cheaper than conventional furnace systems. In addition, microwave heating is much more efficient than conventional furnace heating, as heating is directly produced inside the material. This minimizes the loss of energy due to heating of the ambient. There is a need for more efficient processing techniques. In this study, microwave annealing is used as an alternative to the current postimplantation processing. Arsenic-doped silicon was microwave annealed (with an aluminacoated silicon carbide susceptor) to activate dopant atoms and to repair damage that was caused by ion implantation. Sheet resistance and Hall effect measurements were used to assess the extent of dopant activation. Rutherford backscattering spectrometry (RBS) with ion channeling was conducted to determine the extent of recrystallization. The dopant activation and recrystallization resulting from microwave annealing is compared with that resulting from conventional rapid thermal annealing (RTA) with the same heating profile. The results show that when compared to RTA, susceptor-assisted microwave annealing results in better dopant activation for shorter anneal times under the same heating conditions.

Jan 1, 2015

By Tracy Morris, Weldon Read, Luis Navarro

"During the leaching of anodic slimes, tellurium dissolves into the leach liquor together with copper and must be removed before the solution is sent to liberator cells for copper recovery. Prior to the installation of autoclaves, tellurium was precipitated using raw slimes that caused a recirculation of tellurium in the leaching circuit. After autoclaves were installed the old leach tanks were converted into tellurium reactors utilizing copper chips, steam and agitation to form a copper telluride precipitate. Tellurium levels of less than 10 rng/L are achieved in a timely manner.IntroductionThe electrolytic refining of copper consists of an electrolytic cell provided with an anode of impure copper, a cathode of substantially pure copper (starter sheet) and an electrolyte made of copper sulfate and sulfuric acid [1]. When a direct electrical current is passed between the anode and cathode inside the cell, the impure copper anode dissolves in the electrolyte and pure copper is plated onto the cathode. During this operation, many of the impurities are deposited on the bottom of the cell as an anodic slime residue composed of insoluble chemical compounds. Slimes are a major source of rare and precious metals in the copper industry [2-5],In the Amarillo Copper Refinery (ACR), the anodic copper slimes are sent to the Precious Metals department in order to extract and then refine the gold, silver, platinum and palladium from them. The remaining impurities, in the form of a soda slag or copper slag are sent to the Hayden smelter for further processing. Copper telluride is sent to the Selenium/Tellurium department inside the plant for selenium and tellurium recovery. During the leaching process of the anodic slimes, copper, tellurium, and other metal species in the slimes are dissolved into leach liquor that cannot be returned to the tankhouse unless the tellurium concentration is below 10 mg/L."

Jan 1, 2012

By José Sancho, Julia Ayala, Purificación García, Begoña Fernández

"A study is carried out to see the adequacy of using flying ashes coming out from a Power Station to eliminate the copper present in waste cyanide waters that are generated in gold mines.Tests were carried out to see how effective the use of ashes taken from two Power Stations could become. Later, the tests are made using ashes coming from Narcea Power Station as this station is near the mine under study.The work is centred on looking for an economically adequate solution to close the waste decanting ponds of the mine. After several tests, a solution is reached through filtration in static layers.IntroductionThe use of coal to adsorb some water-soluble substances has been widely studied [1,2,3,4,] both in the treatment of drinking waters and in determined stages of selective detachment of cyanide gold complexes in cyanide lixiviation processes [5]. Flying ashes sent to the atmosphere by Power Stations as a sub-product of the combustion of this combustible are generally made of more of a 70 % of a vitreous aluminosilicated material and of an active residual material which may be changeable making them potentially useable as adsorbents. Nevertheless, the properties of each kind of ashes depend on the characteristics of the Power Station, of the combustibles being used, of the combustion system, etc.The aim of this work is to demonstrate the adequacy of flying ashes to eliminate the copper present in cyanide waters coming from gold mines either by adsorption or precipitation of the metal. For this study, tests are carried out with Asturian ashes which have a low quantity of lime. The results obtained in the tests demonstrate the effectivity of the method used. To be absolutely concrete, the work is carried out to establish the use of these ashes in the closing of Asturian installations of cyanide lixiviation"

Jan 1, 2008

By Christine Wenzl, Andreas Filzwieser, Stefan Konetschnik

"The METTOP-BRX-Technology is a novel manifold electrolyte inlet, which allows improved productivity and production in new and existing tankhouses by achieving higher current efficiency and cathode quality, as well as using current densities higher than 400 A/m2. Two installation examples are shown: Montanwerke Brixlegg AG, Brixlegg, Austria (upgrade of existing tankhouse) and Xiangguang Copper, Yanggu, China (new tank house). Montanwerke Brixlegg AG has been using the METTOP-BRX-Technology since 2005, and converted half of the whole tankhouse to METTOP-BRX in 2011 in order to use a current density of more than 400 A/m2. Xiangguang Copper started up their second tankhouse in May 2011. This tankhouse was constructed in the same way as the existing tankhouse, but was designed for 292,000 t/a cathode copper (existing tankhouse: 200,000 t/a) by using the METTOP-BRX-Technology. This production increase is a consequence of a much higher current density, namely 410 A/m2, compared to 280 A/m2 in the old tankhouse.IntroductionCopper electrorefining has been practised for more than hundred years, the last big change being the implementation of stainless steel cathodes in the 1980s [1], In 2005, the METTOP-BRXTechnology was first introduced. This technology was developed jointly by METTOP and Montanwerke Brixlegg, Austria, and allows improvements in productivity and production in new and existing tankhouses in an economic way. The METTOP-BRX-Technology is a novel manifold inlet that allows improved tankhouse productivity by increasing current density and/or current efficiency while maintaining or improving cathode quality [2]."

Jan 1, 2012

By Rivera Jose Antonio Ore

Top Submerged Lance (TSL) smelting technology is currently used in a wide range of applications in the non ferrous and waste product treatment industries. The use of TSL technology for tin concentrates smelting has been successfully applied at the Minsur Tin Smelter and Refinery at Pisco, Perú. The process is based on the air-cooled top entry submerged Sirosmelt lance, developed by Dr. John Floyd at the CSIRO division of Mineral and Process Engineering in the 1970?s. Advantages of the process include flexibility to operate the lance, main burner of the Sirosmelt furnace, with different levels of combustion stoichiometry which allows us to get from highly reducing to highly oxydising atmospheres in the smelting reactor according to the type of feed we are processing, ability to utilize cheap energy sources such as natural gas, low capital cost and an environmentally friendly operation. This presentation summarises the application of the Submerged Sirosmelt technology for smelting tin concentrates and a variety of tin containing materials like iron dross, copper dross, tin residues, low tin/antimony slags by applying recent metallurgical developments at the Minsur smelter. The impact of new feed conditions and level of impurities on reactor performance with features of process and operation control are described. As a result of these recent advances in tin smelting using TSL technology, the Minsur Tin Smelter and Refinery improved its overall tin recovery, substantially reduced tin inventories and became the second largest tin smelter in the world, currently producing more than 40,000 metric tones of refined tin per year.

Jan 1, 2006

By Oleksandr Liaskovskiy, Sergey Beringov, Sergiy Yatsuk, Timur Vlasenko, Iryna Buchovska

"Working with solar-grade silicon for solar cells application usually meets some difficulties in comparison to polysilicon produced by Siemens method: higher impurities content leads to lower yield, worse electro-physical parameters and poor performance in solar cells application. However some adjustments in ingot production can show significant improvements in quality of final product: crystalline wafers and cells.Recent investigations have shown that solar-grade silicon is suitable for high effective production process such as mono-like multicrystalline wafer production. Production-scale lots made at Pillar show promising results for solar-grade silicon application: high-quality wafers with significantly big crystalline grains of <100> orientation.IntroductionThe standard technology of producing multicrystalline silicon ingots by directional solidification method in quartz crucibles has a number of disadvantages resulting in limited efficiency of solar cells made of multicrystalline material: crystallites of multicrystalline ingot are relatively small (down to 5 mm size), grain borders of crystallites contain parasitic impurities such as metals, silicon nitride etc., crystallographic orientation of crystallites is random. The listed deficiencies are an integral characteristic of the technology which affects the efficiency of solar cells, such as presence of solar cells with low efficiency even at a high level of average efficiency, problems with shunted cells, silicon nitride inclusions, which adversely affect cell efficiency and are centres for silicon carbide formation, impossibility of application of high effective alkaline texturing etc. Also with regard to the targets set by photovoltaic to reduce the cost per Wp in the nearest future, standard technology of multicrystalline silicon ingots production by directional solidification faces certain challenges some of which are hard to overcome due to rather low efficiency of solar cells made of multicrystalline wafers. Therefore alternative methods of multicrystalline silicon production for photovoltaic application having a number of advantages in comparison to traditional technology are developing rapidly."

Jan 1, 2012