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By Thomas Gliick, Jianming Lu, David Dreisinger

"The Boleo project of Baja Mining (Vancouver) will process a mixed oxide-sulfide ore using an acid oxidation and reduction process in seawater to extract copper, zinc, cobalt and manganese. Copper will be extracted via SX-EW as copper cathode, zinc will be recovered as a zinc sulphate monohydrate crystal and cobalt will be produced as a cobalt cathode product after phosphinic acid extraction. Manganese may be recovered from the final solvent extraction raffinate by precipitation as manganese carbonate.The development of the cobalt recovery process (solvent extraction and electrowinning) will be discussed. The pilot plant solvent extraction circuit and subsequent bench and small pilot testing of cobalt electrowinning will be discussed. The Boleo project will produce approximately 1708 tonnes per armum of cobalt metal when fully commissioned.INTRODUCTIONThe Boleo property is held by the Mexican company, Minera y Metalllrgica del Boleo S.A. de C.V. (MMB). MMB is owned 70% by Baja Mining Corp. and 30% by a consortium of Korean companies consisting of KORES - Korea Resources Corporation, LS Nikko Copper, Hyundai Hysco, SK Networks and Iljin Copper. The project is fully financed and is now under construction with an expected startup in early 2013 .Average annual production, for the first six years for each of the metals is forecast as: 56,697 tonnes of copper cathode, 1,708 tonnes of cobalt cathode and 25,364 tonnes of zinc sulphate monohydrate. The project has an average life-of-mine cash cost (based on the three year trailing average metal prices, as of December 31, 2009, in accordance with SEC guidelines) of -$0.29/lb Cu, net of by-product credits for cobalt and zinc and with no credit for manganese production. There is the potential to produce up to 220,000 tonnes per armum of manganese carbonate (- 100,000 tpa contained Mn) via the relatively simple addition of a small number of unit operations to the proposed plant. The recovery of manganese metals from the manganese carbonate intermediate material is discussed in a separate paper in this proceeding."

Jan 1, 2012

By Katragadda Sarveswara Rao

"In view of the increasing importance of processing lean ores as potential future resources, efforts are being made worldwide to develop suitable technologies for the recovery of both nonferrous, base and precious metals. There are various types of low grade ores present in many countries. Gradually, the mineral reserves for production of metals have undergone complex changes with regards to their grades and particularly the physical and chemical properties of the minerals to be separated from each other. So, there is a need for new processing routes or the upgrading of existing technologies to recover metal values that are otherwise unutilized. Accordingly, an overview of the different types of mineral resources and economical processes, based on ore horizons, consumption of energy and reagents and environmental concerns, is made in this paper. In addition, the paper provides a summary of metallurgical and engineering challenges to be overcome when implementing new technologies and concepts with regard to base metal extraction and sulphur removal efficiency.IntroductionLow grade multimetal complex sulfide ores are likely to become an importance source for nonferrous as well as precious metals in the near future. The principle metallic minerals are chalcopyrite, sphalerite, galena, pyrite, pyrrhotite, arsenopyrite, tetrahedrite, boulangerite and cassiterite. Such ores are located throughout the world as multi-pocketed reserves which have present complex challenges with regard to their grades and particularly the physical and chemical properties of the minerals to be separated from each other. Their compositions can vary widely from one deposit to another and even from one location to another in the same deposit, and this poses a problem for the recovering metals present therein. Successful aqueous processing of complex sulphide ores depends on the composition and mineralogy of the raw materials and on their leaching behaviour."

Jan 1, 2012

By Ehsan Vahidi, Fereshteh Rashchi, Ataollah Babakhani, Alireza Zakeri

"The synergistic effect of Cyanex 302 on solvent extraction of nickel and cadmium from sulfate solution with D2EHPA diluted in kerosene was investigated with the aim of increasing separation efficiency. Experiments were carried out within a pH range of 0.1-5.0 using sole D2EHPA and D2EHPA-Cyanex 302 mixtures in different ratios. Increasing Cyanex 302 to D2EHPA ratios in the organic phase caused a left shifting of the extraction isotherm of cadmium and a right shifting of the extraction isotherm of nickel. As a result, optimum separation was found with a Cyanex 302 to D2EHPA ratio of 0.1M:0.5M. In the present system, effect of a modifying reagent such as TBP was studied. The influence of various diluents including kerosene and carbon tetrachloride was also investigated.IntroductionBatteries are popular sources of portable energy. Ni-Cd batteries are manufactured in two main groups of small domestic cells and large industrial batteries with 80% being in domestic use. Ni-Cd cells have various uses, for example in cordless electric utensils, cordless telephones, airplane engine starters, and communicational distribution systems [1].Depleted Ni-Cd batteries are classified as hazardous waste since nickel and cadmium are heavy metals and suspected carcinogens. Given the risk associated with uncontrolled disposal, directions for issuing legislation on disposal and recycling of used batteries have been made in industrialized countries [2]. Recycling of Ni-Cd batteries is important from both economic and environmental points of view. Different methods have been used for recycling these wastes through pyrometallurgy [3], biotechnology [4,5], and hydrometallurgy [1,2].Due to the advantages of hydrometallurgical processes, several studies have been implemented on leaching and solvent extraction (SX) of the used Ni-Cd batteries. Leaching of batteries is usually done in sulfate or chloride media; while solvent extraction has been used in different extractants: two-stage solvent extraction by D2EHPA and Cyanex 272 [6]. Solvent extraction of Cd from leach solutions has been studied using various extractants; Cyanex 301 [1], D2EHPA [7], Cyanex 302 [8], Cyanex 923 [9], Cyanex 272, Tops 99, PC88A [10]. Application of phosphorus based extractants for the solvent extraction studies of Ni such as TOPS 99 [11], D2EHPA [12], Cyanex 272 [2], has been investigated. Separation of Cd(ll), Ni(II), and Co(ll) from chloride leach liquor of spent batteries [13], were explored in the earlier studies. Cd extraction with D2EHPA involves co-extraction of both Ni and Co [14], which causes issues in the separation process efficiency."

Jan 1, 2012

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 Daniel Kim, Ari Rantala

Efficient on-line monitoring of electrolytic cell performance in copper electro-refining has been challenging due to the need for complex electrical measurement systems and the management of the enormous volume of data. Based on Kennecott Utah Copper's innovation Outotec has developed a novel and innovative electrolytic cell monitoring system called CellSense™ System. As the system is based on self-powering from bus bars, wireless communication, on-line adaptive modeling and easy to access information and alarming, traditional obstacles of electrolytic cell monitoring are eliminated. With cell voltage and electrolyte temperature measurements, CellSense System enables real-time cell performance discovery and early reaction to critical production or quality disturbances such as short-circuiting, flow blockages, cold cathodes or electrolyte temperature excursions. During the past few years the system has been delivered to over 3500 commercial cells. In this paper the largest CellSense™ System ever delivered and recently adapted by Kennecott Utah Copper with 1412 cells monitored on-line for high tankhouse performance, cathode quality and optimized operator work flow is presented. Early results and benefits are discussed.

Jan 1, 2012

By Linli Wu, Guangchun Yao

"The influence of deformation on the properties of short-carbon-fiber reinforced 2024 alloy matrix composites was investigated in this study. It was found that the distribution of carbon fibers changed from the random state before deformation to the ordered state that carbon fibers arranged along the direction of rolling and extruding after deformation. Under the temperature range in control, the increase of rolling and extruding temperature would benefit to improve strength and elongation of composites, but was not conductive to improve the hardness of composites. With the increment of total deformation, all the strength and the hardness of composites became greater, nevertheless the elongation decreased. After being rolled and extruded, the strength and the hardness of composites were all bigger than those of composites before being rolled and extruded; moreover, the strength of extruded 2024 alloy matrix composites was higher than that of rolled 2024 alloy matrix composites under the same heat treatment conditions.IntroductionCarbon fibers have been reckoned as very important reinforcements due to the high specific strength, specific modulus, high thermal and electric conductivity, low expansion coefficient and good self-lubricant properties [1-4]. Light metal composites reinforced with carbon fibers, such as carbon fibers in an aluminum matrix, are widely used and studied. Some studies have concentrated on the interfacial characteristic of CF/Al composites in order to search for the way of improving the bonding between carbon fibers and the matrix alloy [5-8], and on the influence of the carbon fiber percent composition in the composites [9-11]. Some researchers began to take interest in the deforming characteristic and failure behavior of carbon fiber reinforced metal matrix composites [12-16]. However, the same with other metal materials, most of CF/AI composites were prepared by some single processes, such as powder metallurgy, extrusion casting and vacuum press infiltration, which caused that the composites products could not be manufactured directly. In order to cover the shortage of the mentioned above processes and get composites products with perfect mechanical properties and dimensional accuracy, the composites should be reworked by rolling, extruding or forging process. Compared with research about manufacturing process, the correlative investigation on the reworking of CF/Al composites was much less evidently, which restricted the application and the further development of CF/Al composites."

Jan 1, 2012

By O. Chemezov, Yu Zaikov, A. Apisarov, A. Isakov

"Silicon deposits containing 99,9 wt.% of main component were obtained by SiO2 electrolysis from chloride-fluoride melts. The operating temperature was varied from 973 up to 1073 K. The conditions for obtaining crystalline fibrous micro- or nanodeposits were determined. The deposits were investigated by ESM methodIntroductionThere are large reserves of natural quartz of high purity in Russia. Processing of this raw material by electrolysis in molten salts produces silicon containing 99.9 weight percent of basic substance.[1]This method is less energy-consuming in comparison to existing methods for producing high purity silicon from gas phase.Another advantage of the electrolytic method for producing silicon from its oxide in molten salts is the possibility of production of high-purity silicon under air atmosphere. It dramatically reduces costs of the electrolytic cell construction, and the operating costs at electrolysis.On our opinion, the main advantage of the electrolytic production from SiO2 in molten salts is a unique opportunity to obtain micro-and nanostructures of silicon deposits. In particular, it is possible to obtain fibrous structures of silicon. The electrolytic method allows smoothly adjusting the thickness and length of silicon micro- and nano-wires by varying the cathode current density and temperature of the process."

Jan 1, 2012

By Renxing Li, Yongyong Gong, Yufeng Cheng, Zhenxing Yin, Xin Cao, Qijie Zhai

"The influence of electric current pulse (ECP) on the solidification structure of SUS430 ferritic stainless steel (FSS) was investigated in the current study. The technology of ECP has been widely used to improve the properties of metals with relatively low cost. The parallel electrodes were inserted into the free melt surface to constitute a current loop. The different influences of three parameters on solidification structure were studied by changing the peak current value, frequency and treating time respectively. The results indicated that the ECP significantly increased the number of equiaxed grains of SUS430 FSS. The as-cast structure without ECP treating was almost wholly columnar, while the number of equiaxed grains of the specimen, which was treated 3min with a peak current of 400kIA, increased to 2698 in the observed surface. To get the best refinement, an optimum range of these three parameters is required and the peak current value plays the most important role.IntroductionFor the lack of nickel resource and the pressure of environment protection, ferritic stainless steel is increasingly adopted to replace the austenite stainless steel because of its low nickel content and good mechanical properties. SUS430 steel is a typical example with excellent performance and relatively low price to replace the application of austenitic stainless steel[1-3]. This type of steel with high thermal conductivity coefficient, low expansion coefficient, good oxidation resistance, excellent stress corrosion resistance and other fantastic characteristics is often used to make components which need to have resistances for atmosphere, water, steam and oxidizing acid corrosion[4]. Since the developing of columnar grains and low toughness at high temperature, its products are easily crinkled and cracked during the subsequent rolling process[5]. The application of ferritic stainless steel is limited by these defects[6-8]."

Jan 1, 2012

By Masatsugu Morimitsu

"The novel smart anode, MSA ™, for electrowinning of non-ferrous metals such as copper, zinc, nickel, and cobalt has been developed by thermal decomposition. The smart anode consists of a titanium substrate coated with a catalytic oxide layer which comprises amorphous or less crystalline oxide coatings. The catalytic layer contains an iridium oxide-based mixture or a ruthenium oxide-based mixture. The smart anode provides a remarkable reduction in cell voltage compared to other anodes, e.g., commercially available coated titanium electrodes and lead alloy electrodes. The test data has demonstrated that a maximum voltage reduction by ca. 30% is possible compared to lead alloy anodes. The smart anode also gives some additional merits in suppressing unwanted deposits on the anode; i.e., deposition of MnOOH, Pb02, or CoOOH. The electrowinning with the smart anode is possible to be an environmentally friendly process with less energy consumption and less anode deposits.IntroductionA coated titanium electrode iridium oxide-based or ruthenium oxide-based catalytic layers is well known as an insoluble anode for oxygen or chlorine evolution in industrial electrolysis such as chloro-alkali electrolysis, electrogalvanizing or electrotinning of a steel, a thin film production by electrodeposition such as copper foil production (CFP), water electrolysis, and electrowinning of nonferrous metals. The anode is commercially produced by thermal decomposition of a precursor solution painted on a titanium substrate, and the decomposition is usually performed at 450 °C or more. The obtained catalytic oxide coating formed on the substrate contains crystalline oxide as an active component to oxygen or chlorine evolution. The author of this paper had met a problem of such a crystalline oxide coating in the application of copper foil production; the anode was unable to use for a long period because of a large amount of lead oxide (Pb02) deposited on the anode, and the cell voltage was seen to continuously increase and drastically rise by the accumulated Pb02. In this case, the voltage reduction by replacing a lead alloy anode with the dimensionally stable anode was initially observed, but was gradually lost and disappeared. Therefore, the author of this paper aimed and investigated to suppress the unwanted side reaction on the anode, and finally invented a new class of coating based on an amorphous iridium oxide mixture in 2003 [!]. The invented coating was obtained at a low temperature thermal decomposition, e.g., 360 °C, and the coating consisted of amorphous iridium oxide and amorphous tantalum oxide. This invention achieved that oxygen evolution potential shifted more negative so that the cell voltage was reduced, and no Pb02 was deposited in the electrolyte of CFP [2,3]."

Jan 1, 2012

By Mingzhou Li, Lin Wu, Changren Tong, Fengli Yang, Shaohua Yang

"According to characteristics of Tm, Yb and Lu enriched oxides composition and problems in its traditional extraction separation process, the computer simulation of a optimized fuzzy extraction separation process, in which three products with high purity(>99.99%) could be obtained at same time, was carried out. Distributing Curves of every element in both organic and aqueous phases were worked out. Distribution rules of rare earth elements in every stage of the optimized extraction process were studied. The computation results of economical and technical index showed the consumption of the acid and base chemical reagents in the optimized process would be saved more than 30%.IntroductionFor the solvent extraction separation process of rare earths, countercurrent extraction process was widespread in the industrial practice. Normally, rare earth ions were extracted by the saponificated extractant and transferred into the organic phase, where the acidic extractant was saponificated by the base firstly. Then, the loaded rare earth ions were stripped from the organic phase into the aqueous phase by the acid. Therefore, the acid and the base were the main consumptions in the process, and the equilibrium acid of the stripped rare earth solution was one of the main pollution resources. Meanwhile, for the heavy rare earths, such as Tm, Yb and Lu, stripping was more difficult, and the equilibrium acidity of the stripped rare earth solution was higher, so the acid consumption increased greatly."

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 E. A. Chavarriaga, L. J. Jaramillo, O. J. Restrepo

"This paper presents the results of the manufacturing ceramic pigments with spinel structure, using methods of synthesis of low temperature. In this work we obtained spinel structures type by the methods of Self-combustion, Coprecipitation, Microemulsion, Gel citrate and Pechini. These methods become an attractive alternative to traditional method (ceramic method), since we can work at a lower temperature, reducing manufacturing costs, lower fuel consumption, less wear on equipment and other environmental and economic implications. Also it is possible to have control over features such as stoichiometry, morphology of the products, reaction times and structures. The products obtained by these routes will be used in the manufacture of ceramic pigments and characterized using different techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM) and UV-VIS spectrophotometry.IntroductionSpinels are ternary oxides AB204, where A and B are cations occupying tetrahedral and octahedral positions respectively. These oxides exhibit interesting electrical, magnetic and catalytic properties [1-4], depending on its nature, charging and intrinsic distribution of ions [5].The most widely used method to prepare spinels has been through solid state reaction, which consists of mixed oxides at high temperatures [6, 7]. In the last years, there have been a strong tendency to use chemical routes for the synthesis of crystalline ceramic particles at low temperatures [8,9]. Unconventional methods currently employed for the synthesis of complex oxides are Gel citrate method, Pechini, Spontaneous combustion, Microemulsion and Coprecipitation. Pechini method [10, 11], based on polymeric precursors, does not require high temperatures and allows stoichiometric control for greater reproducibility. This method involves the formation of a polymeric resin between a metal quelate and polyhydroxy acid of alcohol by polyestirification.Coprecipitation is important for many environmental problems related to water resources, including acid mine drainage, migration of radionuclides in waste repositories dirty, transport of contaminant metals in the industry, metal concentrations in aqueous systems and the technology of wastewater treatment. The coprecipitation process can vary in each case; the partition in the solid phase can be carried out by surface adsorption, ion exchange, surface precipitation, occlusion and formation of solid solution. The formation of solid solution is the result of structural incorporation of the marker in structural support sites resulting in a minor component in the solid solution with the host phase that has a very low solubility of pure solid [12]. Synthesis by gel citrate method allows the use of a route to obtain ceramic pigments from a very simple experimental system in which the stoichiometric control, the size and shape of the particles and the purity of the phases obtained can be controlled more accurately [13]."

Jan 1, 2012

By Ibrahim Yusufoglu, Ahmet Orkun Kalpakli, Cem Kahruman, Sedat Ilhan

"The effects of oxalic acid concentration, temperature, stirring rate and particle size on the dissolution rate of synthetically prepared calcium molybdate were investigated. Dissolution of calcium molybdate in oxalic acid solutions takes place as a series - parallel type reaction. In the first reaction step, which proceeds according to the ""Langmuir - Hinshelwood Mechanism"", calcium aqua oxalato molybdate is formed as a complex chelate intermediate product. In the second reaction step, molybdic acid is formed during the slow hydrolysis of calcium aqua oxalato molybdate, and it reacts rapidly with oxalic acid to form the polymeric hydrogen oxalate dimolybdate chelate as an end product. Activation energies were calculated as 41.4 and 49.9 kJ mol-1 for the first and zero order reactions. The fractional conversion versus time relationship can be given by the following equation.IntroductionMolybdenum is used widely in electric-electronic, metal working, aerospace and aeronautic, nuclear, glass and petrochemical industries because of its high melting temperature and resistance against chemical effects. However, the largest molybdenum consumers are the iron-steel and super alloy industries where molybdenum is used as an alloying element. Industrially important molybdenum minerals are limited to molybdenite (M0S2), powellite (CaMo04) and wulfenite (PbMo04), which are considered as primary molybdenum resources. Secondary molybdenum resources are spent catalysts and scrap [1-4].Molybdenum has been produced by pyrometallurgical processes in the past. Since it is possible to process low grade molybdenum ores and industrial wastes by hydrometallurgical processes, which are more environmentally friendly than pyrometallurgical processes, the importance of the use of hydrometallurgical processes has increased in the molybdenum production industry."

Jan 1, 2012

By Jorge Alberto Soares Tenório, Denise Crocce Romano Espinosa, Luciana Harue Yamane

"The present work investigated the effect of inoculums volume on bioleaching to recover metals from printed circuit boards using Acidithiobacillus ferrooxidans-LR. Printed circuit boards from obsolete computers were mechanically processed by comminution followed by magnetic separation, and the obtained non-magnetic fraction was used in the bioleaching experiments. A shake-flask study was carried out on the non-magnetic fraction samples using a rotary shaker at 30°C, 170 rpm and different volumes of oxidized culture solution as inoculums (%v/v): 5, 10, 20, 30, 40, 50 e 60. The oxidized culture solution was prepared inoculating pre-adapted bacteria Acidithiobacillus ferrooxidans-LR (5%v/v) in 200mL T&K medium. Leaching in acidic ferric sulphate was also performerd. The analyzed parameters were pH, ferrous iron concentration and metals analysis (AAS). The results showed that using 10%v/v of inoculums were extracted 99,2% of copper and 60% of aluminum by bioleaching. Zinc, lead and tin extraction were not influenced by bacterial leaching and extractions rate were obtained by chemical leaching promoted by acid medium. Ferric iron leaching extracted less copper (35%) than bioleaching. SEM analysis shown surface difference between samples of non-magnetic fraction before treatment and after bioleaching, showing corrosion pits formed by the bacteria contact.IntroductionWaste of electrical and electronic equipments (WEEE) has been target of discussion due to environmental, political and economical issues involved. Around 17 million of computers are discarded annually in the world due to malfunctioning equipment or because technologies become obsolete [1,2]. In contrast, only the central processing unit (CPU) of computers weights around 3kg. From this data, it can be calculated that 51 million kilograms of CPU waste are discarded yearly. This calculation was performed considering only the CPUs, disregarding the cathode ray tubes and liquid crystal displays of monitors [3,4]. Because of the amount that has been accumulated, e-waste has become a global problem but also can be an alternative source to recover valuable materials [5,6]."

Jan 1, 2012

By Hongmin Zhu, Kai Huang, Shuqiang Jiao

"Garlic peel was used as the raw material to synthesize the biosorbent for the selective recovery of precious metals from the acid chloride solution. Garlic peel is rich in carboxyl-, amino- and thiol-groups, has the potential of exhibiting high affinity to Au(III) when appropriate chemical modification process was employed. Here in the present study, the biosorbent was prepared by cross-linking garlic peel particles with concentrated sulfuric acid. Adsorption tests for mixing different metal ions such as Au(III), Fe(III), Cu(II), Ni(II) and Zn(II) from various concentrations of hydrochloric acid media indicated that Au(III) was selectively adsorbed on the cross-linked garlic peel gel over the other coexisting base metal ions investigated. The crosslinking mechanism and selective adsorption of Au(III) were also investigated briefly.IntroductionPrecious metals are quite popularly applied in the modern industries such as jewelry, electronics and electrical devices, catalysts in chemical industry, etc. While their high values, limited deposit and quite large demand in industry makes its recovery from the industrial wastes, typically e-wastes, quite necessary. Actually, many techniques have been developed to recycle and recover the precious metals from various industrial wastes effectively in last decades, but the cleaning and ecofriendly processes are still seriously scarce [1]. Taking into account of the typical recovery processes using cyanide lixiviant in the alkaline media, or aqua regia, followed by the further recovery process using activated carbon adsorption or cementation with zinc, iron or aluminum plate or powder, though they both are quite effective recovery processes, if considering the special requirements on safety and ecofriendliness for the modern hydrometallurgical processes, various improved or novel extraction processes are greatly demanded [2]. Recently, the biosorption technology applied to the recover precious metals in the hydrometallurgical process has become a concern [3,4]. Inoue’s research group made great progress in the recovery of precious metals such as gold, palladium and platinum from the e-wastes such as spent mobile phone by using biosorption from the hydrochloric acid media [5,6]. This new hydrometallurgical process exhibits the prominent advantages of being cost-effective for its short process, easy operation and near-zero emission. In the above recycling process for e-wastes treatment, the preparation of biosorbents is the key and backbone of the whole recovery process. For this purpose, they developed a series of suitable sorbents for precious metals recovery by using the tanning-based or cellulose-based biomass such as persimmon peel, grape peel, orange juicing residue, waste cotton, waste paper through the crosslinking process with concentrated sulfuric acid and relative chemical modification processes [7-10]. In the present study, we also applied this technique to prepare the biosorbent of precious metal uptaking by using garlic peels as the raw materials, and investigated the adsorption properties of such-obtained gel in the hydrochloric acid media."

Jan 1, 2012

By Kouji Mimura, Masahito Uchikoshi, Minoru Isshiki

"HfO2 is expected to be a gate dielectric used in ULSI alternatives to S1O2. Although the materials used in ULSI are required to be significantly pure, commercial Hf contains > 2 mass% Zr. It is important to establish a process for removing Zr from Hf. In the present study, anion-exchange separation using a multi-column method was employed. The separation tests were carried out at variety of temperatures and flow rates. The decrease in the flow rate of the mobile phase made the elution curves of both Hf(IV) and Zr(IV) broaden contrary to the case of Co(II), Cu(II), or Fe(III). This is caused by the difference in adsorption rate on the anion exchange resin. In addition, more than one column was connected in series in order to enhance the separation. As a result, the content of Zr(IV) was successfully reduced to 1/100 of that relative to the raw material.IntroductionHafnium is one of the most important materials in modem society. The main applications of Hf metal are as a control rod in a nuclear reactors because of its large neutron-capture cross-section and as an additive to various alloys because of its corrosion resistance [1]. In addition to those applications, attention has been recently paid to HfCh as a high-x"" dielectric used in ultra large scale integration, ULSI, as well as ZrCh, AI2O3 and La2C>3, which are expected to be alternatives to conventional S1O2 thin films [2].The materials used in ULSI are required to have a high purity in order to avoid unexpected errors due to impurities. Furthermore, high purity Hf is indispensable for investigating the intrinsic properties of Hf metal. Thus, it is significant to establish the purification process for Hf from both the industrial and academic perspectives."

Jan 1, 2012

By Tracey Brommer, Britt Elin Gihleengen, Elsa Olivetti, Randolph Kirchain

"Increased demand resulting from the economic and environmental advantages of recycling secondary materials has constrained secondary material supply. As a result of constrained supply, the conventional strategy to maximize recycled content in an individual aluminum alloy must be expanded to maximizing total recycled content in a given production period. This work compares the performance over a two week period of an actual remelter for two strategies; a sequential charge-by-charge optimization framework and an integrated approach that explicitly incorporates the production schedule. Optimizing across the entire two week production is found to increase recycled content and minimize primary and alloying material additions. It is expected that as the scrap material market continues to be constrained by high demand, longer term batch planning strategies that can optimize material allocation will deliver improved performance.IntroductionIntensifying economic and environmental pressure to incorporate secondary aluminum into products is pushing remelters to explore additional strategies and tools to increase recycled content. Aluminum remelters are exploring alternative sources of secondary materials because of constrained secondary material supply and relatively high primary and secondary material cost [1]. Computational models, such as blending models are a tool that could help industrial remelters mitigate supply and cost challenges and thereby increase recycled content. In particular, computational tools can help manage the incorporation of new raw materials of variable quality. Blending models find many industrial applications and have been explored for over sixty years originating with the classic nut-mix problem dating back to 1950’s [2]. Blending models optimize the raw material input to make a desired product subject to a series of constraints such as product specifications and material availability. Deterministic and linear blending model formulations are presently implemented in some industrial aluminum remelters [3]. The primary reluctance of aluminum remelters against computational model implementation is the incapability of their blending models to reflect the intricacy of industrial remelting conditions [4]. For example, to reduce calculation time, industrial aluminum blending models usually optimize a batch plan for a single alloy and are not formulated to optimize several products simultaneously. Since such a model does not include knowledge of subsequent charges in the optimized batch plan, the resulting batch plans tend to deplete the “cleanest” secondary materials leaving the more uncertain and compositionally challenging materials for later charges. As a result, a remelter may override the calculated batch plan or leave certain scrap materials out of the material input to conserve these materials for alternative products scheduled for later production. This work explores an alternative aluminum charge planning tool that can optimize across an extended production schedule and compares it to a heuristic sequential optimization strategy reflecting an industrial remelter."

Jan 1, 2012

By Michael S. Moats, Daniel Kim, Shijie Wang

"The behavior and deportment of lead, arsenic, antimony and bismuth are critical in producing high quality cathode by copper electrorefining. A critical review of research related to these elements is presented along with a comparison to industrial data, where appropriate. These elements exist predominantly in the anode as complex oxides along die grain boundaries. Upon dissolution, Group 15 elements report both to the electrolyte and slimes while lead essentially enters the slimes. The deportment of the Group 15 elements appears to be influenced by several chemical interactions which are discussed. The effect of these elements on floating slimes and anode passivation is reviewed. Under normal electrorefining conditions, lead, antimony and bismuth are thought to enter the cathode through the encapsulation of slime particles. The literature indicates that arsenic enters the cathode predominately by electrolyte entrainment. Finally, areas for future research regarding these elements are presented.IntroductionControlling lead, arsenic, antimony and bismuth is critically important for the production of high quality cathode in copper electrorefining. The reasons for this are twofold. First, ASTM Grade 1 Cathode specifications [1] for these elements are low, as listed in Table 1. Second, they can affect the efficiency of the electrorefining process (e.g., through passivation, current efficiency, slime processing)."

Jan 1, 2012

By V. Bojarevics, K. Pericleous

"A number of different methods have been developed for noncontact electromagnetic treatment of liquid metal and to investigate the melting/solidification processes. Applying AC magnetic field in terrestrial conditions, along with the buoyancy and thermo-capillary forces, results in turbulent flow. The use of a homogenous DC magnetic field allows damping both of the turbulence and the large scale flow at different rates leading to surprising results at some stages. The dynamic interaction of the turbulent flow with the oscillating interface needs to be accounted if it is required to levitate liquid metal of up to few kilograms without the contact to container walls. At the high values of magnetic field some oscillation modes are damped quickly, while others are modified with a considerable shift of the oscillating droplet frequencies and the damping constants from the non-magnetic case. Numerical models are used to investigate behavior of liquid metal suspended in high DC magnetic fields providing microgravity-like conditions with laminar viscosity and heat transfer to the surroundings.IntroductionSince the early Electro Magnetic (EM) levitation experiments [1] in AC magnetic field it became apparent that the levitated liquid metal is prone to oscillation and instability. The EM and electrostatic levitation experiments with liquid metal droplets show difficulties related to confinement stability and a need for complex correction functions to establish a correlation between the measurements and the droplet material properties [2,3]. Intense internal fluid flow is visually observed, apparently being in the turbulent regime for earthbound conditions."

Jan 1, 2012

By Michael S. Moats, Alexander Derrick

"The Winand Diagram was developed and has been used for decades to illustrate the interaction between polarization, mass transport and inhibition on the resulting structure of a metal electrodeposit. Recently, Adcock et al. criticized the Winand Diagram and developed their own structural diagram based on nucleation and plating overpotentials. Their work was based on zinc electrodeposition using a galvanostatic staircase method. This work explores the nucleation and plating overpotentials for copper electrodeposition using conditions typical for primary electrowinning and the galvanostatic staircase experimental technique. Additionally, the effects of organic additives and plating substrate on these overpotentials are reported.IntroductionThe control of electrodeposited structures is critically important to modem electrometallurgy operations to insure proper quality and efficient energy use. Electrodeposition of base metals for primary recovery (e.g. electrowinning or electrorefining), while similar to plating for decorative or device manufacturing, differs in the need to produce deposits that cover large areas and grow to significant thickness. Thus, controlling nucleation and particularly growth of electrodeposits is critically important for base metal electrometallurgical operations.The control of nucleation and growth on an industrial scale is most influenced by five parameters - current density, temperature, metal concentration, electrolyte agitation and additives. The effects of these parameters on electrodeposition are interrelated. To describe their effects on the type ofelectrodeposits generated and provide practitioners with a useful tool, Winand developed what is known as the Winand Diagram [1-2]. An adapted version of the Winand Diagram is shown in Figure 1.Winand characterized electrodeposits using Fischer's classification [3] and plotted the various deposit types versus inhibition on a vertical axis and the ratio of current density to bulk metal concentration on the horizontal axis. Inhibition intensity is a complex parameter and is still not well understood even though Fischer introduced the term in 1960 [4]. Often, inhibition intensity is simplified to equal the concentration of organic additive at the deposit surface and is related to the inverse of the exchange current density of the metal being deposited. The ratio of current density to bulk metal concentration is used to represent the ratio of crystallization overvoltage to mass transport of the depositing ion. As such i/iL could also be along the horizontal axis, where iL is the limiting current density of the electrodeposition reaction."

Jan 1, 2012