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By Kang-In Rhee

Nonferrous metal recycling not only provides energy saving and environmental benefits but also is a significant factor in the supply of various types of metals used in our society. Recycling plays an important role in establishing the sustainability of materials. The total amount of recycled nonferrous metals by weight accounts for less than 5% but their value is larger than 50% compared to ferrous metal recycling which consists of about half of the total metal recycling in weight. This paper describes trends and typical achievements in nonferrous metal recycling and overviews the present and future of nonferrous metal recycling technology and business in Korea.

Jan 1, 2006

By Huang Chao

The thermodynamics analysis on reducing-matting smelting of sulfide ore of lead, antimony and bismuth which use ferric oxide as sulfur fixed agent is first analyzed. Due to the analysis of reaction mechanism, ferric oxide is first reduced to ferrous oxide, then ferrous oxide produce reducing-matting reaction with sulfide ore and reducing agent as reaction equation: MeS+FeO+CO=Me+FeS+CO2. The reaction thermodynamic calculation shows that the reducing-matting reactions of lead sulfide, antimony sulfide, Jamesonite, and bismuth sulfide are feasible, but is infeasible for zinc sulfide. These conclusion provide a feasible method for solve the pollution which produced in the smelting of sulfide ore of lead, antimony and bismuth.

Jan 1, 2006

By Z. Zhang, Zongshu Zou, Nan Wang

"Thermodynamic calculation is applied to make an investigation on the equilibrium phase relations and liquids of CaO-SiO2-Al2O3-FeOx system for different temperatures. The calculated results with FactSage6.1 show that the effect of temperature on the the equilibrium phase relations and liquidus of CaO-SiO2-Al2O3-FeOx system and its sub-systems is appreciable. The liquid phase regions enlarge with increasing temperature from 1573K to 1873K, while the primary phase fields reduce distinctly.IntroductionThe main oxide components of vitrified bottom ash slag are CaO, Al2O3, SiO2, Fe2O3, MgO, and Na2O, accounting for more than 90% of the bottom ash by weight[1]. During slag processing, the knowledge of thermodynamic properties and liquidus temperature in the related slag systems is highly required [2, 3], which is not yet available. Through literature survey [4-6], it is clear that the systematic information on the concerned complex slag system is scarce. So far the engineers in the field have to make assumptions of the thermodynamic properties of the simplified oxide system, without taking into consideration the interactions of the different oxide components, which hinders the development of the slag valorization and utilization. In order to provide thermodynamic properties for the application of the vitrified bottom ash, the six-component oxide system (CaO-MgO-Al2O3-SiO2-FeOx-Na2O) is highly required. A preliminary phase diagram of the CaO-MgO-Al2O3-SiO2-FeOx-Na2O system can be obtained from extrapolation of the thermodynamic functions of constituent subsystems such as CaO-SiO2-FeOx-MgO, CaO-SiO2-FeOx-Al2O3, CaO-SiO2-Na2O-MgO and CaO-SiO2-Na2O-Al2O3. In this work, the equilibrium phase relation and liquidus of CaO-SiO2-FeOx-Al2O3 system, one subsystem of the concerned complex slag system, are calculated and the effect of temperature is also discussed."

Jan 1, 2012

By R. J. Batterham

This paper sets the scene for the Australian-Asian Pacific Course and Conference on Pyrometallurgy for complex materials and wastes. The relentless presence of competitiveness is rehearsed as the source of the current trends towards continuous improvement and benchmarking. While this might be expected to lead to more spending on pyrometallurgy, the opposite appears to be the case. The paper examines the reasons and suggests that we face an increasing challenge for selective developments that can lead to sustainable competitive advantage - both in mineral and in waste processing.

Jan 1, 1994

By Yoshimasa Oda

The tank house of Tamano Smelter has adopted a high current density electrolysis operation applying PRC (Periodic Reverse Current) method and before 1991, it had materialized both high production capacity of 161,000 tons/year and high labor productivity. However, recent rapid rise of Japanese currency in foreign exchange market has urged us to further exert our efforts in reduction of labor cost. In order to achieve this goal of labor cost reduction, we have completed, in 1994, our phase four production expansion project which incorporated significant re-structuring of the organization and we have accomplished annual production of 191,000 tons/year. This project can be outlined as increase of number of cells for electrode exchange per day in the commercial electrolysis process to meet the increased number of cells and increase of the capacity of impurity treatment process. These improvements were done with minimum installation of new equipment and facilities and with achievements in efficiency and manpower saving of the existing facilities. Together with these improvements, rationalization in the starting sheet section was carried out by changing the material of mother blanks as well as changing their maintenance procedures. At the same time, the crane in this section was modified to enable automatic operation by a fuzzy control. As a result, we were able to save manpower equivalent to 5 operators in this section. With these improvements, the production capacity was increased by 18% and labor productivity by 25%.

Jan 1, 1996

By K. Ono

A new process for extraction of titanium metal from its oxide is demonstrated. In this process, row material to be reduced is titanium oxide synthesized from ilmenite. The reducing agent is the Ca+CaCI2 two-phase mixture. TItanium is elaborated in the medium consisted of liquid Ca, Caq and solid TI02 at the temperature range 1200 to l300K by means of mixing mechanically the ingredients in the reactor into a smooth paste. Fluidity of the feed which enables continuous scheme depends on the CaCl2 content. The oxygen level of the reduced titanium is the range 500 to 1000 mass ppm varying with the operational conditions. The Ca+CaCI2 reducing agent is taken out from the electrolysis of CaC12 at 11401(, and this CaCl2 is produced by aqueous chemistry conversion using Cl2 gas recycled from the electrolysis.

Jan 1, 2001

By Guozhu Ye, Eric’ Burstrom

"Despite of numerous solutions for recovery of zinc from EAF dust have been suggested and tested in laboratory scale over the last three decades, Waelz kiln process is still the most dominating process for treatment of EAF dust. Few of the proposed alternative methods have gone beyond the laboratory tests. This paper will give you insights to some of the concepts that have been pilot tested at MEFOS. The innovative aspects of these concepts will be shown and the major results will be highlighted. These include the following concepts: - Production of a crude zinc oxide product with low halide content for zinc electrowinning using a DC furnace with hollow electrode- Production of a bypass filter dust containing more than 50%ZnO by injection of EAF dust to the electric arc furnace during refining combined with a bypass filter system- Elimination of zinc ferrite by CaO treatment for electrowinning with EZINEX process - Selective reduction of iron oxide in zinc ferrite for simultaneous recovery of ZnO andmetallic ironIntroductionRecovery of zinc from EAF dust is dominated by the Waelz process since EAF dust has been classified as hazardous waste by EPA in the early 1980´s. A large number of alternative processes have been suggested and tested without commercial success due to two major reasons [1]:- High content of chlorine and fluorine for the pyrometallurgical alternatives- High content of ZnOFe2O3 for the hydrometallurgical processesMany innovative concepts for treatment of EAF dust for zinc recovery have been pilot tested at MEFOS in the past 20 years. This paper will review some of the concepts focusing on the two problems mentioned above."

Jan 1, 2008

By Liping Li

A comprehensive three-dimensional two-phase mathematical model was developed to represent a channel type reactor with intense bottom gas agitation. Tracer dispersion and particle tracing methods were used to conduct the analysis based on the solution of the Navier-Stokes equations. Different operational parameters, such is gas volume flow rate. bubbler separation aspect ratios and liquid Input flow rates, were investigated for the purpose of reactor optimization. The numerical calculations were compared with experimental results obtained at the University of Missouri and a good general agreement was observed. Relatively low longitudinal mixing was observed characterizing the system as a "plug-flow" type reactor, in contrast to the intense vertical mixing, under the conditions investigated. Some general mixing characteristics are also discussed In connection to the behavior of other metallurgical reactors.

Jan 1, 1996

By L. Dornelles, M. H. Prediger, R. de C. de S. Schneider, D. A. R. Lopez

In this work it was evaluated the environmental impact of sunflower plantation for biodiesel production. It was considered, for life cycle analysis (LCA) of sunflower in familiar agriculture in the South of Brazil, data collected in 23 experimental farmings with sowing in the period from August to November (2006 -2007). The LCA has considered the plantation conditions, energetic efficiency, man power, diesel volume, type of machines, fertilizers and pesticides used. From the analysis carried through it was evidenced that the sunflower produced in small scale does not need the use of tractors to have an excellent productivity and low impact. Therefore, the sunflower can be cultivated, with the necessary cares, in periods that do not compromise the man power for other cultures and the sunflower is an alternative so that the familiar property can produce biodiesel.

Jan 1, 2008

By KNona C. Liddell

The time and spatial dependence of component and species concentrations during in situ uraninite leaching have been modeled using a reactive transport model based on partial equilibrium between reactive minerals and the solution. The flow field is represented by mixing cells in series. The effects of the H2O2, (NH4)2CO3, and NH4HCO3 component concentrations have been simulated, and results are presented for a one-dimensional flow field.

Jan 1, 1995

By T. Taniguchi

The existing Mitsubishi Process line at Naoshima Smelter and Refinery has been operating successfully since 1991, and its present production capacity is 270,000tpy of copper. Furnace relining works have been carried out every two years to coincide with the compulsory bi-yearly boiler inspection, but the next target is to extend the furnace refractory life to four years, while still undergoing the mandatory boiler inspection every two years. Although the damage of hearth bricks beneath lances in the Smelting furnace was a matter of concern, it was reduced by controlling gas velocity and evening solid distribution to each lance. The life of bath level bricks in the Converting furnace was also a concern, but four-years continuous use of the bricks was achieved in the course of the last two campaigns. Several other improvements were also carried out to the cooling systems during the shutdown in 2005 to ensure longer campaign life. This paper summarizes recent improvements implemented to enhance the advantages of the Mitsubishi Process.

Jan 1, 2006

By Burkhard Seeger et al.

The oxidation of copper sulfides can be highly accelerated in the presence of nitrous gases (NOx) as reaction catalysts. Sulfur and sulfate are simultaneously produced in this highly exothermic reaction. This process, carried out in sulfuric acid medium, is performed at an approximately normal pressure and at a temperature of around 110 °C, in a closed container, adding either oxygen or air. The oxidation is automatically controlled through a computer. The process covers the following steps: Catalytic oxidation, filtration and crystallisation of the hot concentrated liquid, electrowinning, mother liquor treatment through jarosite formation, recovery of dissolved copper and zinc and regeneration of industrial water, and non-soluble residue treatment with extraction of sulfur and recovery of silver and gold. No combustibles are needed. No air is contaminated, and no waste water is produced. Solid residues are in a stable, non-toxic and non-corrosive state of equilibrium. Risk of accident is low. Investment costs are small compared to those of the comparable pyrometallurgical process, and production costs are competitive.

Jan 1, 1999

By K. Kashiwaya, N. Hiroyoshi, H. Furuya, N. Sumiya, M. Tsunekawa, M. Ito

"The number of hybrid vehicles is increasing and this is causeing an increase in waste nickelmetal hydride batteries. The cathode activating agent of batteries is made of nickel hydroxide and the anode activating agent is an alloy of nickel and rare earth elements. Conventional rotary kiln methods cannot recover the rare earth elements, and hydrometallurgical treatment of crushed product consumes large volumes of agent. The physical separation of the anode alloy from the cathode hydroxide would make it possible to reuse the alloy. The authors have reported separation of anode and cathode components in the large size fractions using a newly developed dry magnetic separation method. Wet magnetic separation has been applied to the powder fraction and about 90% anode purity was achieved. This paper reviews experimental results from previous publications and proposes an integrated treatment process for crushed nickel-metal hydride batteries.IntroductionEnvironmentally-conscious clean energy vehicles have attracted much attention in developed countries and particularly hybrid vehicles are increasingly mass-produced as low emission vehicles. Hybrid vehicles have both a gasoline engine and an electric motor to save on gasoline usage and a nickel-metal hydride battery is used to store electric energy. The battery contains Nihydroxide and Co as the cathode activating agent and an alloy of Ni and mischmetal (mM), a rare-earth element mixture consisting of La, Ce, and Nd, as the anode hydrogen adsorption component. In conventional recycling, the Ni and Fe are recovered with a rotary kiln-electric melting process and the Co and mM go to the slag component [1] and hydrometallurgical treatment of crushed product consumes large volumes of agent. Japan Oil, Gas and Metals National Corporation have proposed a low energy and low cost recycling treatment process combining the physical and chemical treatments and the authors are investigating the physical treatment process."

Jan 1, 2008

By M. G. King

In 1982, Asarco operated six smelters and refineries producing primary copper, lead, zinc, silver and gold. At that time Asarco was still reliant on its custom smelting and refining roots and mined only 25% of its smelting and refining capacity for copper and 10% of its lead smelting and refining capacity. By 1992, Asarco had been reshaped to become largely an integrated primary metal producer operating four smelters and three refineries. Zinc is no longer refined and the mining capacity has been increased to meet 100% of copper smelting and 50% of lead smelting needs. Only one custom smelter is in operation. This paper describes the metallurgical changes and challenges which have occurred in this restructuring of Asarco's operations while maintaining Asarco's position as one of the largest non-ferrous metals producers in the world.

Jan 1, 1993

By V. T. Taniguchi

A process for large scale chromatographic separations using a continuous chromatography technique is described. The process combines the advantages of large scale batch fixed column displacement chromatography with conventional analytical or elution continuous annular chromatography (CAC) to enable large scale displacement chromatography to be performed on a continuous basis (CDC). Such large scale, continuous displacement chromatography separations have not been reported in the literature. The process is demonstrated with the ion exchange separation of a binary lanthanide (Nd/Pr) mixture. The process is, however, applicable to any displacement chromatography separation that can be performed using conventional batch, fixed column chromatography.

Jan 1, 1989

By Arvind Thekdi, Cynthia Belt2

"Waste heat from industrial operations in metals industry represents 20% to 50% of the total energy used in most manufacturing plants. Reduction and recovery of waste heat offers the most attractive and cost effective method of reducing energy intensity for an industrial plant to meet corporate energy saving goals. It is possible to reduce or recover 30% to 60% of the available waste heat by using conventional and readily available technologies. Projects to reduce or recovery waste heat may offer less than 3 years payback to as short as a few months. This paper presents information on most commonly used methods for waste heat reduction and recovery in the metals industry operations. It describes the methods and use of analysis tools that would allow a user to estimate energy savings, CO2 or GHG reduction potential, and economic benefit and includes appropriate case histories.Waste Heat SourcesSources of waste heat abound with the metals industry. While the overall quantity of energy is high, the sources are distributed throughout a plant. The largest source within the metals industry is within furnace exhaust / flue gases. This includes the high temperature gases from burners in process heating such melting, calcining, and sintering operations. It also includes lower temperature gases from heat treat, dryers, and heaters. Lower temperatures are also found after post processed hot gases. This could include heat left after heat exchangers, regenerative systems, thermal oxidizers, and emission control systems. Other hot gases include air used in direct and indirect cooling.While waste heat in form of exhaust gases is readily recognized, waste heat can also be found within liquids and solids. Waste heat within liquids includes things such as cooling water, heated wash water, and blow down water. Solids can be hot product at discharge after processing or reactions are complete. Indeed, not only is energy wasted in the hot metal that slowly air-cools, but additional energy may be used in providing air or water-cooling to increase the speed of cooling. Other waste heat sources are not as apparent and include things like hot surfaces, steam leaks, boiler blow down water, etc. Table 1 and Figure 1 show several major sources along with the temperature range and characteristics of the source."

Jan 1, 2011

By Edgar Blanco

A thermodynamic and experimental investigation to develop a new process for converting molybdenite concentrate to molybdenum dioxide by a water-vapor oxidation process was carried out. In addition, the behavior of rhenium and selenium in molybdenum concentrate during the process was investigated. The kinetics of the reaction were determined by measuring the weight change of a sample with time in water vapor at temperatures between 700-1000°C. The results were analyzed by a Shrinking Unreacted Core model under chemical reaction control, which showed an activation energy value of 102 kJ/mol. To determine the behavior of rhenium and selenium, their concentrations in the molybdenum sulfide and the product molybdenum dioxide were measured by the use of ICP. While most rhenium remained with the molybdenum dioxide after the water vapor oxidation, almost all selenium volatilized. These results agree with thermodynamic analysis.

Jan 1, 2006

By Jr. Santafé, Lucas L. da Costa, Felipe P. D. Lopes, Sergio N. Monteiro

"Residual vegetable fibers as leftovers from crops, industrial activities and consumable items are realistic options to be incorporated into low cost polymeric composites with the aim of replacing other commonly used materials. The present work assesses the technical properties of epoxy composites reinforced with residual fibers from the coconut fruit, also known as coir fibers. Based on these properties, an evaluation was carried out on these coir fiber/epoxy matrix composites to be used as building panels and furniture in comparison with conventional materials.IntroductionThe utilization of waste from industrial activities is presently recognized as important way in preventing environmental pollution as well as developing new products. This utilization would also generate employment and contribute to environmental improvement in global scale. Among such wastes, those from lignocellulosic materials represent a considerable potential for practical application. In fact, about 2.5 billion tons of these materials are currently available [1], and their fiber content is an important option for composites fabrication. Actually, lignocellulosic fibers are now replacing synthetic fibers as reinforcement in resin matrix composites owing to specific advantages such as low cost, biodegradability and renewable characteristics [2,3]. Moreover, as abundant waste, some of these lingocellulosic fibers could help reducing the use of traditional materials like wood and plastics in many industrials applications. This would prevent further stress on the environment caused by depletion of dwindling resources associated with forests and petroleum."

Jan 1, 2008

By Xian-Dong Zhou, Guo-Sheng Sun, Jianzhong Luo, Hong-An Guan

"Oxygen utilization rate of the pretreatment process which adopts biological contact oxidation method for slightly polluted supply water is relatively low, less than 10%, usually lower than 3%. So the aeration amount is not determined by calculated value of oxygen demand when doing process design, but by the ratio of gas and water. The aeration way of the biological pretreatment process for slightly polluted supply water was introduced in this paper. In the foundation of the principles of mass transfer kinetic theory and experimental data, the change law of DO (dissolved oxygen) and ammonia in the aeration tank was analyzed to explore aeration method which will help to improve the overall effectiveness of handling capacity.IntroductionThere are many kinds of filler used in the biological contact oxidation process, such as flexible solid filler, composite filamentous filler, powdery clay filler, particle ceramic filler and so on. Regardless of the different forms of filler, there are a couple of common points in the function of the aeration[1,2]: (1) The aeration process in biochemical tank not only provides adequate oxygen for the biological reaction, but also plays as a role of stirring water; (2) Biochemical reactions mainly happen in the upper reaches of tank, but seldom at down-streams.This paper, from the perspective of changing aeration way, discussed the feasibility of improving the effectiveness of biochemical reactions without increasing aeration amount, which would have some leading significances for the operation and management of similar projects."

Jan 1, 2008

By Rzyman Michal, Nakamura Takashi, Shibata Etsuro, Grabda Mariusz, Oleszek-Kudlak Sylwia

"Tetrabromobisphenol A (TBBPA) and many systems based on the synergistic effect of brominated organic compounds with Sb2O3 are extensively used as effective brominated flame retardants (BFRs) in many materials such as plastics and textiles. Thermal degradation of BFR containing plastics leads to the formation of hydrocarbons and gaseous compounds such as HBr and SbBr3. Our thermodynamic considerations indicate that these gases can act as bromination agents for metallic oxides such as ZnO, Cu2O, CuO, PbO and FeO. Moreover, these metallic oxides have the thermodynamic tendency to brominate easier than does Sb2O3. The aim of this study was to investigate experimentally the reactivity of ZnO with 1) HBr originating from the thermal decomposition of TBBPA and 2) SbBr3, which is formed during thermal degradation of brominated flame retardant plastics. The thermal treatments of the mixture of compounds of interest were investigated by thermogravimetry coupled with mass spectrometry.IntroductionTetrabromobisphenol A (TBBPA) and many systems based on the synergistic effect of brominated organic compounds with Sb2O3 are extensively used as effective brominated flame retardants (BFRs) in materials such as plastics and textiles. For instance, 4.5 million tons of flame retardant plastics containing BFRs are produced in Japan each year. Thus, in thermal treatments such as the incineration and melting of solid wastes, BFR containing plastics are intentionally or unintentionally included in the wastes. Thermal degradation of BFR-containing plastics leads to the formation of hydrocarbons and gaseous compounds such as HBr and SbBr3 [1-5]. Our thermodynamic considerations [6] indicate that heavy metal oxides such as ZnO, Cu2O, CuO, PbO and FeO should easily react with HBr prior to Sb2O3 and also with SbBr3, the main gaseous product in the thermal decomposition of TBBPA, forming low boiling point metallic bromides suitable for the volatile separation of heavy metals. The metal oxides are also expected to qualitatively and quantitatively affect debromination and decomposition of the flame retardant."

Jan 1, 2008