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By Shinya Hodoshima

A catalysis pair of tetralin dehydrogenation / naphthalene hydrogenation has been proposed in the present paper as a liquid organic hydride for operating stationary fuel cells. Catalytic naphthalene hydrogenation, having been commercialized since the 1940s, proceeds to generate decalin via tetralin as an intermediate. The storage capacities of tetralin (3.0 wt%, 28.2 kg-H2 / m3) are lower than decalin (7.3 wt%, 64.8 kg-H2 / m3) but both tetralin dehydrogenation and naphthalene hydrogenation are much faster than the decalin / naphthalene pair. Moreover, existing infrastructures such as gas stations, chemical tankers and tank lorries are available for storage, transportation and supply of hydrogen. With respect to the stationary fuel cells with large space for hydrogen storage, tetralin as a hydrogen carrier is superior to decalin in terms of fast hydrogen supply or power density. Rapid hydrogen supply from tetralin under mild conditions was only accomplished with the carbon-supported metal catalysts in the ?superheated liquid-film states? under reactive distillation conditions. In contrast to the ordinary suspended states, the catalyst layers superheated in the liquid-film state gave high catalytic performances at around 250OC. As a consequence, both serious coke formation over the catalyst surface and excessive consumption of exergy were prevented simultaneously.

Jan 1, 2006

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

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

Jan 1, 2013

By John A. S. Green, J. Gilbert Kaufman, Subodh K. Das

"The aluminum industry is a leading proponent of global sustainability and strongly advocates the use of recycled metal. As the North American primary aluminum industry continues to move offshore to other geographic areas, such as Iceland and the Middle East, where energy is more readily available at lower cost, the importance of the secondary (i.e., recycled metal) market in the U.S. will continue to increase. In the past, the recycling industry had been synonymous with the collection of aluminum beverage cans. However, as the opportunities for aluminum recycling have multiplied in motor vehicles, building and construction, and aerospace, these market are getting additional scrutiny for optimization of recycling strategies.Accordingly, the secondary industry can now draw upon a much wider range of product forms and alloys for its raw material, but this in turn brings issues of alloy sorting, impurity content, and control as the material is remelted and recycled into new product forms. The purpose of this paper is to take an integrated, industry-wide approach to look at the recovery of material from demolished buildings, shredded automobiles, and aging aircraft, as well as from traditional cans and other rigid containers. Attempts will be made to assess how the different alloys used in these separate markets can be recycled in the most energy efficient manner.IntroductionIn his recent book “Aluminum Recycling”[1], Mark Schlesinger points out that in traditional extractive metallurgy, the raw material used to produce a metal is mined from the earth and then is separated from other gangue minerals and impurities. In aluminum recycling, however, the ore body consists of scrap metal found on the ground, rather than in it. He further notes that scrap comes with its own variety of gangue and impurities such as painted coatings, other metal attachments, and even dirt and other contaminants. So, while the recycling process still requires some refinement and expenditure of energy, the effort and energy involved is much less than traditional mining."

Jan 1, 2008

By M. Cloete, C. MacLagan, A. Newall

This paper initially gives a brief overview of Zinc Corporation of South Africa Limited (Zincor). The original design parameters of the Zincor roasters are compared to the current operation, and the requirements for efficient roasting are listed. Roaster operational problems experienced during the early to mid 1990's are outlined. A description of the investigation and the outcome to increase overall roaster availability are given. The history and the development of the use of oxygen at the Zincor roaster operation, with an account of the associated operational experiences, are explained.

Jan 1, 2000

By Yuan Zeping

The distributions of impurities in the copper melt, the slag and the gas phase in copper flash smelting process were under study in the Guixi smelter, particularly during operating conditions of high oxygen enrichment with production of high grade matte. Several methods for the removal of impurities such as As, Sb and Bi in the copper smelting process were developed and implemented at the Guixi smelter. This paper described the effects of high oxygen enrichment, elevated matte grade, high temperature and high production rate on the distribution of impurities, methods adopted at the smelter for the removal of impurities, and the associated benefits in the utilization of these removal techniques which include the mathematical model for material blending, high thermal intensity operation at the flash furnace, extended converter blowing, and injection of slag modifiers consisting of Na2CO3 and CaO powder mixture to the converters and anode furnaces.

Jan 1, 1999

By A. Pagliero

The coulombimetric reduction method has been used as an evaluation technique for Pb-Ca-Sn anode corrosion in the LIX-SX-EW process. The proposed methodology involves three consecutive steps, i.e., cleaning, oxidation and reduction. They are carried out in the same experimental unit, in solutions containing 180 g/L H2S04 with and without the addition of cobalt. The authors have worked in a wide range of oxidation current densities, from 150 to 500 A/m2 for in a period from 0.5 to 120 hours. It can be concluded from the results that there would be a linear relationship between the applied electrical charge I*T (Coulomb) and the anode corrosion expressed as transformed Pb mass (mg), for solutions with or without the addition of cobalt. The exception is that for the last one the corrosion rate is 5 times faster, which was observed for every layer. From the evaluation of different corrosion layers, one can point out that its composition is mainly in the form of sulphate. In the presence of cobalt, about 67% of Pb would be as sulphate (PbSO4), about 27% as a basic oxide (PbO) and only 6% as oxide PbO2 on the surface. From this result, it appears that great transformations occurred in the metal/sulphate interface. Without the addition of cobalt, the proportion of oxide Pb02 on the surface increased up to 11.5%. According to the previous statement and considering that Pb was found mainly as sulphate, the authors recommend its determination be used as quality selection criterion. Its evaluation should be performed in the acid solutions with 200 ppm cobalt addition at an oxidation current density of 300 A/m2 for a period of 24 hours.

Jan 1, 1999

By Levent Özmen

Colemanite is a mineral containing varying amount of boron that is found in abundance in Turkey. It has a good possibility to be used as a flux in iron and steel industry. In this study a review of the use of colemanite, as a flux agent in steel production has been carried out and various related aspects such as its influence in metal-slag reactions, solubility of lime and magnesia in the slag are discussed along its performance in several points of views including its technical and environmental usage characteristics. Positive and negative factors of using this material as a flux are also underlined.

Jan 1, 2006

By T. Maruyama

The Tamano Smelter of Hibi Kyodo Smelting CO. ,Ltd. went into operation in 1972. The Flash Smelting Furnace that was originally adapted was equipped with electrodes that were attached to the settler substitute of the slag cleaning furnace. Later the development of our own original coke combustion technology was promoted and a new Tamano Type Flash Smelting Furnace (T-FSF), without electrodes, was put into operation in 1988. The technology of coke combustion and combustion the burner have continued to improve. As a result the copper losses in the slag have been reduced as well as a stable operation has been achieved. Furthermore, this has been accomplished while increasing the concentration feed and the matte grade The current objective is to continue to strive for high matte grade operation and to raise production efficiency while paying attention to the important subject of copper losses in the slag. In this report, the data related to the copper loss in the slag reduction are presented along with the influence of the thickness, settling time and coke. The recent operation conditions of the T- FSF are also presented.

Jan 1, 2003

By Xiangjun Zuo, Lifeng Zhang

"Printed Wiring Board (PWB) is a platform upon which microelectronic components such as semiconductor chips and capacitors are mounted. It is also called printed circuit board (PCB). In the PWBs, the organic substances are approximately 72%. The main composition of organic substances in PWBs is ethoxyline resin bromide or ethoxyline resin chlorinate. Depending on the different application and design of the PWB, various metals may be used in the manufacturing process, including precious metals such as copper, lead, silver, gold, platinum, and toxic metals such as mercury, cadmium, barium, gallium, cadmium, lead, bismuth. The current paper reviewed the recycling process for waste PWB materials, including mechanical recycling, combustion for energy recovery and different pyrolysis processes, such as vacuum pyrolysis, atmospheric inert pyrolysi and flux pyrolysis process, and hydrometallurgical recycling process.Backgrounds of Electronic ScrapsProduction and use of electrical and electronic equipment (EEE), such as TV sets, computers, mobile phones and many other daily-life items, have dramatically increased over past decades, while the lifespan of many products becomes shorter"". The rapid innovation in technology in past decades has resulted in availability of cheaper and better electronic products in the market. Thus the production of waste electrical and electronic equipment (WEEE) is also increasing, with estimates of 20-50 million tons per year being generated worldwide2), and it is a problem that governments and policy makers have to handle W). WEEE is also called ""E-wastes"" or ""E-scraps"". From the points of view of recycling and the valuable materials in the used EEE, ""E-scrap"" is more appropriate than ""E-waste"" since the used EEE are not real wastes to be dumped but had much benefit to recycle. In the US, it was estimated that over 315 million computers between 1997 and 2004 and 185 million computers between 2004 and 2007 would become obsolete 5). E-scrap is the fastest-growing part of the U.S. garbage stream 6). It is estimated that only 20% of the E-scrap generated within the US is currently collected and treated, with as much as 80% being unaccounted for7)."

Jan 1, 2011

By M. Furuta

Tamano Smelter of Hibi Kyodo Smelting Co., Ltd. has been operating without a slag cleaning furnace (SCF) since its start-up in 1972. It has used its own developed coke combustion technology, the Tamano-Type Flash Smelting Furnace (T-FSF). The coke combustion technology that is the core of the process, along with the installation of a computer guided system and the improvement of the concentrate burner combustion in the T-FSF have all contributed to having acceptable copper loss levels in the slag without using a SCF. However, recently, because a high concentrate charge rate has been used in order to achieve a high matte grade in the T-FSF, a short settling time has been experienced and copper losses in the slag have become difficult to maintain at a lower level. Furthermore it is estimated that copper losses will further increase after the completion of the next expansion because with the aim of having a higher matte grade operation at 67% less coke will be charged and the reduction effect of the settler will be smaller. Therefore, in order to maintain the copper losses in the slag within proper levels the installation of SCF was decided. This paper, describes the operation before the introduction of SCF along with some theoretical considerations of slag chemistry.

Jan 1, 2006

By M. M. Coleman

An investigation of the behaviour of sphalerite, chalcopyrite, galena and pyrite during flotation was conducted on selected circuits in the Brunswick Mining and Smelting Corporation Ltd. concentrator in Bathurst, NB. Samples were collected from 59 locations and analyzed for Zn, Pb, Cu, Ag, Fe, As, Sb, Sn, Bi and S. Metal balances were computed using the CAMP Material Balance Program (MATBAL 5) and the metal recoveries for each cell and circuit were calculated. An automated image analyzer interfaced with an electron microprobe was programmed to measure the size of sphalerite, chalcopyrite, galena and pyrite grains in each sample. The percentage of each mineral occurring as free grains and the relative amount of each mineral present in binary and ternary particles was calculated. The recoveries and losses of Pb, Zn and Cu are compared with the amount of liberated and unliberated galena, sphalerite and chalcopyrite present in the concentrates and tailings.

Jan 1, 1989

By D. G. C. Robertson

Counter-current staged reactors offer several advantages over batch reactors for mass transfer between two phases. Several metallurgical reactor designs have utilized the counter-current principle, e.g. the WORCA and QSL processes. But before the principle can be widely adopted, it will be necessary to overcome several significant problems. These include the need to minimize longitudinal mixing in a single reactor or to use several separate staged reactors and to carry out different reactions in sequence, e.g. phosphorus oxidation and sulfur reduction. Theoretical and experimental approaches to these problems will be discussed in the paper.

Jan 1, 1988

By Jeffrey Shepherd, Scott R. Smith, Eduard Guerra

"Electrochemical and spectroscopic evidence for the dissolution of a Au electrode by meso-2,3- dimercaptosuccinic acid (DMSA) from an acidic LiCl04 electrolyte is presented. Near the potential of zero charge, DMSA was determined to form a stable layer on the metal surface but at more anodic polarizations, DMSA was displaced from the metal through an oxidative process. The anodic displacement of the layer from the electrode resulted in a small amount of Au that was detected in the electrolyte using atomic absorption analysis. The extent of Au dissolution, was monitored while holding the potential of the electrode for 24 hours at the thermodynamic Eo/H,O in LiCl04 electrolytes containing 10 mM DMSA. This routine resulted in detectable quantities of a soluble Au-DMSA complex in the electrolyte and the greatest leaching was observed at a pH = 2.0. At room temperature, the leaching rate was stable at 10.9 µg cm·2 hr·' however, upon increasing the temperature to 50.0°C, the rate of Au dissolution increased yielding an average rate of extraction of 40.1 µg cm·2 hr- 1. Interestingly, after the first 12 hours of leaching at 50.0°C, the leaching current decreased dramatically suggesting surface passivation which prevented further Au extraction. The implications of this process in the industrial leaching of Au will be discussed.IntroductionThe use of cyanide in the industrial process of leaching Au from ores has raised concerns regarding both operational safety and environmental issues surrounding the disposal of spent leaching eftluents in tailings ponds. Depending on the chemical nature of the processed ore, the spent solutions that are released into the tailings ponds can contain toxic cyanide, either dissolved or complexed with different metals and may pose serious risk to wildlife as well as freshwater contamination to nearby water systems. Because of these issues, some recent studies have focused on the exploration of more environmentally-friendly molecules to selectively leach Au with appropriate kinetics. However, to effectively leach Au into an aqueous solution, a suitable ligand that reacts to form a stable chemical bond with Au is needed to form soluble Au complexes that can be later recovered [I]. Recently several sulfur bearing alternatives have been shown to leach significant quantities of Au in aqueous solutions. These include thiourea [2], thiocyanate [3], and thiosulphate [4]. However, alkylthiols are also known to quickly form a stable covalent Au-S bond [5], but have been relatively understudied in term of their ability to leach Au in solution, even though some short chain thiols are water soluble and relatively nontoxic."

Jan 1, 2012

By Hong Yong Sohn

On the occasion of this symposium in my name, I reflect upon the contributions of my academic mentors and early associates who helped shape my professional career. I was fortunate to have these people around me during my graduate work and at the start of my professional career. In forming my view of the technical field and career, they represented academia, research institutions, industry, and different parts of the world.

Jan 1, 2006

By Leszek Blacha

Since several years aog there is noted an increasing importance of the metallurgical vacuum technologies. This refers mainly to the extra furnace steel treatment processes, melting of steel and special alloys in the induction and arc vacuum furnaces, as well as refining processes of nonferrous metals. In the presented work, there is discussed a phenomenon of evaporation of volatile components of metal bath under reduced pressure with description of kinetics of this process. In this article are presented are the evaluation of the mass transfer coefficients in the melt and gaseous phase. Based on results of our own research on removal rate of impurities from liquid copper (bismuth, lead) in vacuum refining process, it is determined the thickness of hypothetical boundary layer in the gas phase. This allowed to formulate a general kinetic equation defining the evaporation rate of gaseous components from metal bath. The values of mass transfer coefficients determined from this equation were compared with experimental results by other authors working on the evaporation effect of melt components of metal alloys.

Jan 1, 2006

By P. J. Moor

Britannia Refined Metals Ltd. was built in 1931 to refine the lead bullion produced at the Mt. Isa mine in Queensland, Australia. Several periods of expansion and development have taken place over the intervening years, leading to major increases in the refining capacity for both lead and silver. A plant for treating recycled lead-acid batteries was added in 1976. This was redeveloped in the early 1990's to utilise Isasmelt technology for the smelting operations. Most recently the No. 2 refinery kettle floor was extended to enable it to process lead bullion produced from two Imperial Smelting Furnaces (ISF), at Britannia Zinc Ltd. in Avonmouth, England and at MIM Hüttenwerke in Duisburg, Germany. This expansion included the provision of a plant for the hygienic handling of drosses and skims. This paper briefly describes the present primary refining operations and gives an update on the most recent developments in the process metallurgy and operating practices that have taken place.

Jan 1, 2000

By Isadora Dias Perez, Monica M. Jimenez Correa, Jorge A. Soares Tenorio, Denise Crocce Romano Espinosa

The generation of mining waste has been the subject of environmental, economic and social concern. Alternative and sustainable methods of recycling metals technologies are desired. The present work focuses on the application of the ion exchange technique for the extraction of metals contained in a lateritic nickel mining effluent. The Purolite S950 chelating resin was used in the present work because it has the ability to adsorb transition metals present in an acidic solution. The experiments were carried out in a batch varying the pH in the range of 0.5–2.0. 1 g of resin was placed in contact with 50 mL of solution and stirred for 120 min at a speed of 200 rpm and temperature at 25 °C. The results demonstrated that the affinity of the resin varied with pH. The adsorbed metals were only copper, manganese, magnesium and zinc. The most extracted metal was copper, corresponding to 37%, when the solution was conditioned at pH 2.0.

Mar 1, 2018

By Gavin Lind

The Minerals Council of Australia (MCA), through its Minerals Tertiary Education Council (MTEC), builds capacity in higher education in the core disciplines of mining engineering, metallurgy and minerals geoscience. Over the past fourteen years, this all-of-industry approach in securing the long-term supply of these critical skills (which remain a chronic skills shortage for the Australian minerals industry) through nationally collaborative programs across sixteen Australian universities delivers spectacular and sustainable results for the industry. These unique, world-first programs are built on a healthy platform of dedicated industry funding and in-kind support and forms part of the MCA’s broader uninterrupted, sustainable education and training pathway to increase workforce participation, workforce diversity and workforce skills, regardless of the business cycle in the industry. This paper will highlight the origins, iterations and current successful programs of MTEC, including its future vision, and presents a mechanism for industry and academia to collaborate to address future professional skills needs in the minerals industry globally.

Jan 1, 2014

By F. Nava-Alonso, O. Alonso-González, A. Uribe-Salas, R. Pérez-Garibay

"Cyanidation is the most used method to recover gold and silver from their ores. In this process, other metals besides gold and silver may sometimes dissolve and interfere with the efficiency of extraction. Copper is one of those metals, reaching concentrations as high as 1000 mg/L in some cyanidation plants, making difficult the extraction and purification processes, and increasing the operating costs.This preliminary work was intended to study the feasibility of using amines to form a precipitate and to eliminate copper from a synthetic solution containing high copper and cyanide concentrations, as is the case of some cyanidation effluents. The solid formed is removed from the solution using conventional filtration techniques. Seven amines were evaluated at different pH values and amine additions. Up to 90% of copper present may be removed at the natural pH of the effluent (alkaline). The remaining copper would permit to recycle the solution back to the cyanidation process. IntroductionCopper is generally considered the most problematic metal in gold leaching due to the rapid formation of copper cyanide complexes when some readily-soluble minerals are processed (e.g., azurite, malaquite, cuprite, chalcocite and bornite). The copper solubilization as cuprous cyanide complexes leads to a significant economic penalty in terms of excessive cyanide consumption and high cost for cyanide elimination. When activated carbon is used to recover gold and silver, the copper-cyanide complexes decrease the efficiency of the process because of the competition of the cuprocyanides with the aurocyanide for the adsorptive sites on the activated carbon (Rees and Deventer, 1999).Several techniques have been developed to attempt to overcome the problems caused by the copper presence in cyanidation solutions, notably: acidification-volatilization-regeneration (AVR), ion exchange-electrolysis or solvent extraction-electrowinning (Lu et al., 2002). In this work the use of some amines is proposed to remove the copper-cyanide complexes by precipitation of a copper-cyanide-amine solid. The process was evaluated for different amine additions and pH values, using copper-cyanide synthetic solutions of composition similar to that presented by some cyanidation plants with high copper."

Jan 1, 2008