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By Laura Garcia H, Juan Carlos Gonzalez Islas, Luis Garcia Lechuga, Pedro Alberto Ramirez Ortega

"Electrochemical studies were performed to silver recovery from industrial wastes (radiographic films) on litanium flat electrode using a filter press-type electrochemical reactor with vertical orientation (known as REOV-01), as counter electrode was used a mesh-type DSA. Voltammetric studies were employed to fmd the current range under which silver reduction occurs. Using chronopotentiometric studies with controlled current, homogeneous deposits were obtained on the surface of the Ti electrode, to a current of -210 mA during 120 minutes to a constant linear flow velocity of 15 Lmin-1 was achieved 97% of silver recovery from industrial wastes. Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy studies corroborated the presence of silver on Ti flat electrode. In addition, the silver concentration in the solution after the experiments was 1 ppm below environmental requirements. This indicates the viability of a filter press-type electrochemical reactor with vertical orientation (REOV-01) for silver recovery from radiographic filmsIntroductionIn recent years, the industrial sector has shown an increase in the use of silver due to new applications in different areas. In sectors such as photography, the consumption of silver has declined as a result of the boom in digital photography. However, the use of silver in radiographic applications has not shown greater variation (47.16 Moz), as the image quality is essential for diagnosis in various fields, such as medicine. All the silver used in photographic applications is discarded completely (solid or in effluent). At the present, several countries have been involved in silver recovering from industrial wastes due to the economic value and environmental impact they represent. The main source of silver recovery is the wastes generated by the photographic sector. Various technologies have attempted to recover silver contained in these wastes. However, they have not fully satisfied the requirements of maximum recovery, nor environmental level (less than 5 ppm) of silver in effluents [1,2]."

Jan 1, 2014

By Duck Jae Lee, Kwan Ho Kim, Ji Whan Ahn

"In Korea, reutilization of constructions waste is gaining an increasing attention as generation of construction waste is projected to increase continuously. In current practices, the concrete waste is simply crushed and used as a low application such as paving, back filling, etc. In this study, a new process was developed comprising of heat pretreatment, autogenous milling, and density separation for complete reutilization of concrete waste. Firstly, the concrete waste was crushed using autogenous milling. The coarse size fractions from autogenous milling have a density of 2.5g/cm3 and a water absorption ration 3.0%, which meet the specification of the first class of KS F 2573. The fine size fractions were further separated using a hindered-settling column into two products 1) underflow, 2) overflow. The underflow sample was a high quality fine recycled aggregate which can be used for concrete making, and the overflow sample was an enriched cement material can be also used for CO2 sequestration by mineral carbonation. Introduction Kwan Ho Kim1, Ji Whan Ahn2, Duck Jae Lee1, Hee Chan Cho1 Recently, the importance of resource recycling is gaining a greater attention due to the increasing price of natural resource. Recycling is beneficial for not only the management of waste, but also the reducing of consumption of natural resources and huge energy consumption to treat of natural resource. The construction and demolition waste comprises the major industrial waste generated in Korea. It increased to 54 million tons in 2004, and is projected to increase to over 300 million tons in 2020, as many buildings reach the end of their 30 years life. Among total waste, the proportion of concrete waste was about 30% in Korea. Due to its large volume, recycling of concrete waste is the most important aspect of the waste management. In the current practices, the concrete waste is simply crushed and used as a recycled aggregate. The recycled aggregate has a low quality and most of them are down cycled for usage as paving material, back-filling material, concrete bricks, etc. It cannot be reused for replacement of natural aggregates because cement mortar is not separated perfectly from aggregates. These kinds of recycled aggregates tent to be weaker, more porous and have a higher value of water absorption. When these aggregates are used in concrete making, there are problems of higher total water demand, low compressive strength and durability [1-5]. And recycled fine aggregate is not almost recycled due to its low quality. In this study, a new processing circuit is developed to produce not only highquality recycled coarse aggregates but also fine aggregates and cement material from concrete waste."

Jan 1, 2008

By Esa J. Peuraniemi

Copper smelting to form blister in one single step has been possible for a long time even from low grade concentrates. In spite of obvious benefits, it has been economically viable only with few special raw materials having high enough Cu/Fe and Cu/S ratio. Outokumpu Blister Flash Smelting is currently applied at three operations, and three others will be commissioned in the near future. With typical chalcopyrite concentrates two main obstacles have prevented wider adaptation of direct blister processing: slag formation and heat generation. Oxygen potential in the reaction shaft must be high in order to produce blister with targeted sulfur content below 1%. When large amount of iron is oxidized, as well as sulfur, copper is inevitably also oxidized into slag. High copper amount in substantial tonnages of slag lead on to costly down stream recovery operations to obtain discardable slag. Almost complete oxidation of sulfur and iron releases a high amount of heat which traditionally has been solved by lowering oxygen enrichment of the blast leading on to oversized off-gas line and acid plant. One challenge in direct blister smelting relates to the attack of aggressive high-copper containing slag against furnace refractory lining. In continuously operated Outokumpu Direct Blister Flash Smelting this is taken care of by preventing vigorous melt movement in the settler. Stable bath conditions and stationary slag against refractory lining enable the formation of a protective autogenous layer between aggressive slag and vulnerable refractory. These direct blister smelting challenges are addressed from equipment and process development point of view. New solutions to overcome the obstacles are presented and discussed.

Jan 1, 2006

By Lucas Nana Wiredu Damoah, Lifeng Zhang

"The use of electromagnetic field to remove suspended particles from metals such as aluminum by pushing to the boundary has been well studied. However, the potential of this method is yet to be exploited for the removal of inclusions from silicon. Considering the increasing amount of Top-cut SoG-Si scraps year upon year, there is the need to harness all the potentials of technologies to recycle this materials to ensure sustainability. This study investigates, and discusses new results on the effect of processing parameters such as composition, coil current, and frequency on the removal of inclusions from silicon under high frequency AC electromagnetic field.IntroductionThe solar cell silicon making industry requires pure and clean silicon in order to maximize the conversion potential of the solar cell material. The conversion efficiency of solar cells is limited by minority carrier recombination at dislocations and those intra-granular defects such as impurities, small clusters of atoms, or precipitates [1]. Recent global developments in the energy sector with a drive for the production of clean, reliable, and affordable energy have stirred a rapid growth in the production of photovoltaic (PV) cells.[2] Thus over the years, silicon based PV cells has seen a lot of growth as it has a PV market share of over 90 % [3] either as single-crystalline silicon, or multi-crystalline Si (MC-Si), or amorphous Si [4]. MC-Si produced by directional solidification of solar grade silicon melt dominates the silicon PV market. During the directional solidification process, SiC and Si3N4 particles within the melt are pushed by the solidification front to the top of the ingot which is the last to solidify. Therefore the top of the ingot is cut generating what is known as top-cut solar silicon scraps. The Si3N4 particles are mainly from the coating material at the inside surface of the silica crucible and from the air absorption during solidification process. The SiC particles mainly stem from the carbon reduction process of the primary production of silicon [5]. For sustainability the silicon in the top-cut silicon scraps must be recovered. Therefore methods for removing non-metallic particles, such as SiC and Si3N4, from the silicon are important in order to recycle the top-cut scraps to a useful feedstock for the silicon solar cells manufacturing."

Jan 1, 2012

By Maria Kuttig, Christian Ruback, Gerhard Tober, Petra Maier

"It has been demonstrated that there is a strong relationship between work hardening with various post heat treatment and cyclic deformation behavior of structural steel S275. This study contributes to a project developing a process for the complex forming of steel, which combines rolling and bending. Due to the complex geometry of the final work piece, the deformation degree varies greatly. The forming temperature, as well as post heat treatruent, influences recrystallization processes in dependence of the local deformation degree, resulting in inhomogeneous microstructure of the work piece, which affects the quasi-static and dynamic properties. Cyclic creep and hardening or softening has been monitored during constant amplitude loading at stresses near fatigue strength in normalized condition. Work hardening, stress relief or recrystallization influence the cyclic deformation behavior and produces cyclic creep effects. Cyclic softening or hardening and creep were observed to occur in parallel. To what extent these properties are noted depends on the deformation degree.IntroductionThis work is part of a research project developing a new process for the three dimensional forming of steel. For the final product the fatigue strength influenced by the forming parameters is very important. Due to its complex geometry, the formed final plate has different deformation degrees. This leads to different recrystallization behavior and heat treatruent will have different effects on the microstructure. The peak deformation degree cp of the plate will be around -0.5 what leads to the analysis using rolling from 22 mm to 13 mm of thickness. The quasi-static material properties are very important for calculating the preliminary design. However, work pieces which are cyclic loaded need fatigue tests to describe the in-service material behavior. [l] For the prediction and to guarantee the wanted life-time of the part cyclic deformation tests are important. [2, p.23-32] When it is assumed that the work piece will only loaded in cyclic tension, fatigue testing will be done from zero to a maximum force value. In preliminary tests this value is the tensile fatigue strength from a Smith diagram. During processing, here forming, work hardening takes place resulting in strengthening. Therefore, in further tests maximum load can be increased to monitor cyclic deformation mechanism in more detail. However, to study cyclic creep and hardening and softening data should be evaluate over sufficient life time and should not fracture too soon."

Jan 1, 2013

By S. Goto, S. Yamashita, K. Hata

"The average consumption of zinc dust for purification of zinc leaching solution is more than 25 kg per tonne of electrolytic zinc. Authors proposed to remove impurities in zinc leaching solution by electrolysis instead of cementation by zinc dust. The effects of copper and arsenic on electrodeposition of cobalt in zinc sulfate solution were examined fundamentally using a potentiostat. It is observed that cobalt is easily deposited on a cathode at potentials under -480mV with arsenic. Mesh cathodes of stainless steel and lead anodes were used in a small electrolytic cell and the electrolyte was circulated through 'the electrodes during the electrolysis. The effect of electrolyte circulating rate , pH, cell temperature, current density, and concentration of copper and arsenious ions on removal of cobalt were studied. Removal of Cd and Ni are also examined.IntroductionCobalt is difficult to remove from a zinc leaching solution by a simple cementation reaction using zinc dust. However, it is easily precipitated by zinc dust with co-addition of arsenious or stibinous oxide and copper ion in practical operations(I), (2), (3). The consumption of zinc dust for purification is 16-152 kg per tonne of electrolytic zinc and 65% of this zinc dust consumption is used for cobalt purification. The average retention time for purification of cobalt is 4.5 hours (1). A more economical process for purification is desired instead of zinc dust. The mechanism of this acceleration effect of copper and arsenious oxide on removal of cobalt are explained by the authorsas follows; a galvanic cell is formed between zinc dust and copper which is precipitated firstly, and cobalt is reduced on copper as Co-As alloy by this galvanic current(2). This assumption was confirmed in experiments using a galvanic cell with a membrane( 4). The following galvanic reactions occur between zinc dust and copper precipitate; on copper cathode,2H+ + 2e -= Hz(g)2Coz+ + 2HAs02 + 6H ++ 10e -= 2CoAs + 4HzOand on zinc anode,Zn = Zn = 2+ 2e –This galvanic current becomes almost zero in a zinc sulfate solution which includes only cobalt and no arsenious oxide, and cobalt is weakly deposited on a copper cathode. Cobalt deposition requiers a high degree of cathodic polarization. However, the galvanic current flows almost constantly in an electrolyte, which includes arsenious oxide, and the cathode potential is kept at about -500mV. Cobalt is precipitated as Co-As on the cathode.The authors assumed that cobalt may be removed by electrolysis at a very low current density instead of zinc dust and the following experiments were carried out. In the first part of this paper, the fundamental experiments using a potentiostat on the behaviour of cobalt in zinc sulfate solution are described. In the second part, the results of the electrolysis are reported. Cobalt is removed by a new type of an electrolytic cell, which was desigoed to <Iccelerate the rate of deposition of cobalt. The removal of cadmium and nickel in a solution which includes cobalt and arsenic are also examined."

Jan 1, 1997

By B. J. Jody

This paper describes a one-step thennal-treatment process, developed at Argonne National Laboratory, to remove all organic contaminants from the glass-fiber waste that is generated during the glass-fonning process. The recovcred glass fibers can then be recycled into new glass fibers or new glass products without adversely impacting the operations of the glass industry or the quality of its products. Our process involves shredding the waste to a manageable size and then processing it at temperatures below its melting point to remove the polymeric-coating layer. The glass industry generates more than 60,000 tons of glass-manufacturing waste annually in the glass-forming process alone. Recycling of this waste stream can keep this non-biodegradable waste out of the landfills. In addition, use of recycled glass lowers energy costs, by an average of about $5 per ton as compared to using virgin raw materials to make virgin glass fibers. This process will also reduce the emission of C02 by 17,400 tons a year and it will also reduce the emission of nitrogen oxides. Economic analysis of our process shows a potential payback of less than 2 years.

Jan 1, 2003

By Ian G. H. du Preez

It is illustrated how differences in the basic chemistry of individual metal ions can be exploited to develop new or improved separating agents. Factors like coordination number preferred by the specific metal ion, the degree of coordinate saturation reached by the metal ion and its relation to the phase transferability of the complex species, kinetic factors as opposed to thermodynamic factors controlling the success of the separation, the nature and type of the donor atom employed in a separating agent in relation to the preferences of the metal ion, the significance of stereochemical factors and the hydrophobicity of the media are some of the important factors which are discussed and applied for the development of pa1ladiwn(TI) and nickel(TI) specific separating agents, respectively.

Jan 1, 1999

By Kenji Morinaga, Hiromichi Takebe

"Ge-S binary glasses in the range 57 to 90 at %S at 0.5 to 3 at %S intervals were prepared by a conventional melting technique using fused quartz ampoules as melting containers. Impurities contaminated during preparation process are evaluated by IR spectroscopy. The causes of impurity contaminations are discussed. Density data in a systematic series of Ge-S glasses is demonstrated. IntroductionSulfide glasses are of particular interest for new laser and nonlinear optical materials in the near-infrared and infrared regions [1]. Sulfide glasses have the features of low-phonon-energy and high refractive index with moderate rare-earth ion solubility. The low-phonon-energy is favorable for the reduction of nonradiative rate for the emission of rare-earth ions. The high refractive index results in a high radiative-rate and in a high third-order nonlinearity. However, impurities may degrade the superior optical properties of sulfide glasses.In this work Ge-S glasses were prepared by a conventional melting technique. Impurities contaminated during the preparation process are evaluated and their causes are discussed for future improvements. The measured densities of Ge-S glass samples were compared with the results of previous studies [2], [3]. Ge-S glasses have some favorable properties for practical .applications including non-toxicity, good thermal and chemical stabilities."

Jan 1, 2000

By Kerri-Ann Hue, Kerry Hasapidis, Ken Babcock, Patrick O'Hagan

"Metallic nanoparticles exhibit properties that are significantly different from individual atoms or bulk materials. Their applications are diverse and have varying uses in areas such as cancer treatment, biochemical sensors, nanoelectronics, and drug delivery. For each application extensive characterization must be performed in order to probe the unique properties of these nanoparticles. In this study, ultra-high resolution mass sensors consisting of MEMs-fabricated, suspended microchannel resonators (SMRs) were used to determine the size and concentration of metallic nanoparticles. With femtogram (10- 15 g) mass resolution, ultra-high resolution mass sensors can weigh individual particles suspended in fluid, and so measure their mass, density, and size. Particle size analysis with these sensors provides excellent accuracy and resolution compared to mature technologies such as light scattering. This technique also provides quantitative information via the ability count particles.IntroductionThe unique electronic, chemical, and optical properties associated with nanoparticles vary with their size, shape, and composition[ 1-4]. These properties are attributed to increased surface area and nanosized mean free path of electrons to the particle surface. Nanoparticle colloidal solutions have been prepared and are commercially available. In recent years, noble metals such as gold, copper, and silver have been extensively researched[5-7]. In order to tailor the optical, electronic, and electrical properties of nanoparticles, size and shape must be controlled. For many applications a monodisperse colloidal solution is ideal. Methods of size characterization include Transmission Electron Microscopy (TEM), Dynamic Light Scattering (DLS), and Electrophoretic Mobility Measurements to name a few[6, 8]. Although TEM can provide shape and size distributions, sample preparation requires that samples be dried on a metal grid and cannot be analyzed in solution. DLS uses curve fitting algorithms that while useful for determining mean particle diameters are not ideal for polydisperse colloidal solutions. New technologies are therefore needed to accurately determine the particle size distributions of metallic nanoparticles."

Jan 1, 2011

By F. J. Hogan

In early 1982 Atlantic Cement Company, a wholly-owned subsidiary of Newmont Mining Corp. will come on line with a new water granulating grinding facility at Sparrows Point, Maryland to produce 800, 000 tons a year of separately ground granulated blast-furnace slag. The process and product will be unique to the United States. This paper will review some initial investigations undertaken to evaluate the cementitious properties of granulated slag. The effect of slag fineness on strength development is discussed and data is presented showing a relationship between glass content and hydraulicity and grindability of slag.

Jan 1, 1982

By Antonio Luraschi

The constituents iron, oxygen, silica and cop- per are of principal interest in slags utilized in pyrornetallurgical processes for producing copper. Accordingly, phase relationships in the.Cu-Fe-0-SiO2 system are important when one considers the physico- chemical behavior of slags. These phase relation- ships for the quaternary and constituent ternary systems are developed from available information. Isothermal composition and composition-oxygen potential diagrams, and oxygen potential-temperature diagrams are utilized to describe the&apos; important relationships.

Jan 1, 1976

By Ovidiu Pasca

Several improvements in converter equipment and operation at BHP Copper have reduced the converter cycle time as necessitated by an increase in flash furnace output. The resulting higher intensity performance of the Peirce-Smith Converters has had a major impact on the dust handling and off-gas cleaning systems. This paper describes work carried out on the design of a new converter hood with particular reference to the thermal analysis and hood performance aspects. Changes in converter cycle time and campaign life as result of the process and equipment improvements are discussed in a separate paper.

Jan 1, 1999

By L. Klinger, T. Werber, LA Levin, A Katsman

"The process of catastrophic carburization known as ""metal dusting"", whereby a solid metallic material is converted into fine particles in a carburizing atmosphere, was analyzed. It was shown that this conversion is the result of plastic deformation and subsequent fracture accompanying diffusional phase formation in the near-surface layer. The process is controlled by internal stresses arising during phase transformation. Competition between stress generation and relaxation may result in the attaining the ultimate strength in the near-surface layer and its fracture. Such a mechanism of metal disintegration may occur in a certain temperature interval depending on the kinetic and geometrical parameters of the system - the diffusivities of the alloy's components, the ratio between specific volumes of the new and the old phases, and the ultimate plastic strain. The temperature interval for disintegration of carbon steel, the rate of disintegration, and the period of the disintegration cycle, were evaluated and compared with experimental data. IntroductionCatastrophic carburization, known as ""metal dusting"", consists in conversion of a solid metallic material into fine particles. The process occurs in a carburizing atmosphere at elevated temperatures. The corrosion product, usually named ""coke"", consists of metallic particles dispersed in a loose carbon matrix. Under industrial conditions metal dusting takes place, for example, in a gas mixture of CO and H2 or in hydrocarbon environments. Steels, nickel- and cobalt alloys are susceptible to this kind of wastage in the temperature range 400-800°.A mechanism of metal dusting in steels was proposed by Hochman [1] and later developed by Grabke and coworkers [2-5]. According to the proposed model, the process consists of the following reaction steps:"

Jan 1, 1996

By Dirk Verhulst

The Altair process employs digestion of ilmenite ore in concentrated hydrochloric acid, solvent extraction to concentrate Ti in a purified stream and spray hydrolysis to produce a TiO2 hydrate, followed by final calcining and milling. HCl gas is regenerated by pressure-swing distillation and reinjected in the leaching solution. All chloride streams are recycled. Chromium compounds generally remain in the residue. Solvent extraction provides flexibility for the removal of naturally occurring radioactive elements (NORMs) present in some ilmenites. The process was previously tested at a 5 t/day feed scale. Recent work at pilot scale (40 liter reactor) led to further improvements. Recovery of Ti in solution is now at least 90% with ilmenite ores, while crystallization at lower temperature lowers the amount of Fe in solution to about 5 g/l and improves solvent extraction, which is now conducted in columns. Higher Ti and lower Fe concentrations in the SX eluate improve the economics. A new formula for pigment production via spray hydrolysis produces a pigmentary base with a narrow particle size distribution.

Jan 1, 2003

By William Bourcier

Geothermal Brines are a significant potential source of valuable minerals and metals. These brines are water that is heated by the natural heat flow from the depths of the earth. Hotter brines, typically with temperatures greater than 120°C, are used to generate electricity. Lower temperature brines are directly used to supply thermal energy to applications such as agriculture, aquaculture and process/domestic heat. The geothermal waters have had intimate and lengthy contact with the layers of the earth?s crust that they flow through, resulting in dissolution of minerals and metals from the rocks, and solution into the hot water. These aqueous solutions can be processed to recover minerals and metals. Some potential products include silica, zinc and lithium, along with other materials. Recovery of minerals and metals from geothermal brines can be viewed as ?solution mining by nature?, followed by application of known or new hydrometallurgical techniques for isolation and purification. This paper discusses the opportunities, the processes, the challenges, the current status, the economics and the potential for recovery of minerals and metals from geothermal brines.

Jan 1, 2006

By Carla Lupi, Mauro Pasquali

"Photographic technology is based on light sensitivity of silver halides that, because of silver properties, are capable of forming photographic images. Photographic laboratories and hospital departments because of digital photographic systems less use this technology today. Nevertheless recovery of silver is still advantageous because environmental problems related to Ag ions danger to biological system. Many processes have been studied to treat silver containing photographic bath: cementation, chemical precipitation and electrowinning. In this work, after preliminary voltammetric tests, a batch electrometallurgical process has been studied to completely deplete the silver containing photographic fixing baths. The effect, of silver concentration in the electrolyte, varying over the range 0,2-1 g/L, bath stirring and current density ranging from 10 to 500 A/m2 on process yield and deposit quality, has been investigated. Introduction Photographic wastes, electronic scrap and spent catalysts constitute the main sources of materials for silver recycling. Among those silver secondary sources, the photographic discharged material could be still important and useful, even if photographic laboratories and hospital departments, because of digital photographic systems, less use photographic technology. Several processes have been developped in order to recover silver used in the field of photography from both photographic solutions and scrap film paper[1-5]. Fixing solutions are very complex baths but, because of silver position in the electromotive series, electrolysis could represent an advantageous method for silver recovery. Electrolysis produces high purity silver without generating new pollutants, while the fixer can be reused: obviously it is necessary to purge off a portion of this solution in order to avoid the excessive build up of other deleterious compounds into solution. A tested recovery method was constituted by the dissolution of silver from X-ray films with concentrated nitric acid. Internal electrolysis and external electrolysis methods were carried out using a steel electrode as cathode and a copper electrode as anode [6]. Silver recovery from photographic chemical solutions has been also performed in a special cell [7]: the solution is supplied to the bottom of a non-agitated cell having a vertically elongated form and including a central anode enclosed by a cathode. An other study discloses the use of an electrolytic cell comprising at least one anodic compartment and one cathodic compartment: the solution is treated in the cathodic compartment and then recycled in the anodic one [8]. A more recent work proposes the use of zirconium cathode for the recovery of silver from photographic fixing solution [9]: studies carried out by cyclic voltammetry showed that about 98% of total Ag can be recovered with an electrical efficiency close to 92%."

Jan 1, 2008

By Kouji Mimura, Tamas Kekesi, Yongfu Zhu, Masahito Uchikoshi, Minoru Isshiki

"The formation and anion exchange sorption of chloro complex ions can offer a great potential to be utilized for the separation and purification of metals in aqueous solutions. Available stability data were primarily used to estimate the predominance of chloro complex species, indicating the feasibility of such separations. Anion-exchange sorption functions, describing the equilibrium distribution of a number of important elements have been determined by the batch equilibrating method in the practical HC1 concentration range. Various oxidation states were stabilized by the addition of appropriate agents. Tendencies in oxidation, complex formation and anion exchange sorption were confirmed by spectrophotometric investigations. Based on the fundamental results, anion exchange processes have been developed for the purification of iron, cobalt, copper and zinc. The efficiency of separation was assessed and the procedure optimized by the analysis of experimental elution curves. Results have demonstrated that by properly controlling the oxidation states and HC1 concentrations, practically all the impurities can be eliminated. Computer programs have been developed to estimate complex formation and redox equilibria, to screen and correct analytical data, to determine distribution coefficients and to evaluate efficiencies of separation.IntroductionBase transition metals have long been used as the staple materials in various fields of industry. In general, there has been an increasing tendency in purity requirements but recent advances have created a rapidly increasing demand for ultra-high purity metals. To give a few examples, ultra high purity copper can be used as bonding wire and interconnection in integrated circuits, or as material for superconductor stabilizing, high-field magnets, beside its use in cryogenics and ultra high vacuum technology [1]. Iron holds promises as a constituent element in the ß-FeSi2 material to be applied in new opto-electronic devices [2] and it is currently used, together with chromium and manganese, in the production of special magneto-optical materials for digital recording. The use of ultra high purity manganese and chromium in semiconductor technology is evolving. Although not considered a transition metal, zinc is also treated here because of the major significance in compound ZnSe semiconductors [3], and the possibility to purify it by the anion exchange method."

Jan 1, 2000

By H. Y. Sohn, Haitao Wang, Moo Eob Choi

"A novel ironmaking technology is under development at the University of Utah. This technology produces iron directly from iron ore concentrate by gas-solid suspension reduction. Hydrogen is the main reducing agent for high reactivity and for the elimination of carbon dioxide release in this ironmaking process. The direct use of concentrates allows bypassing the problematic pelletization/sintering and cokemaking steps in the steel industry.Intrinsic kinetics of the suspension reduction of magnetite concentrate particles by hydrogen has been measured. Experiments were carried out in the temperature range of 1423-1673 K, other experimental variable being hydrogen partial pressure, the amount of excess hydrogen and particle size. Under most experimental conditions, 95% reduction was attained within several seconds, which presents sufficiently rapid kinetics for a suspension reduction process. The reaction kinetics followed the nucleation-and-growth equation, and a rate equation that contains all the effects of the experimental parameters has been obtained.IntroductionWith the rapid increase in steel production, it is critical to control CO2 emissions which is the main greenhouse gas. It is inevitable to release a huge amount of CO2 when coke and/or coal are used as the main reducing agent in producing iron. As one of the methods to reduce the CO2 emission from ironmaking, the utilization of the gaseous reducing agents and fuels, including hydrogen, has been investigated [1-6]. The use of such gases forms the basis for a new ironmaking technology under development for producing iron directly from fine concentrates by a gas-solid suspension technology. This technology would reduce energy consumption by about 40% of the amount required by the blast furnace and drastically lower environmental pollution, especially CO2 emission, from the steel industry [4]. This is accomplished by adopting H2-based reductant and bypassing pelletization/sintering and cokemaking steps. Unlike other gas-based alternative ironmaking processes using shaft furnaces or fluidized-bed reactors, the suspension reduction technology is a high-intensity process because it will not suffer from the problems that other processes do when operated at high temperatures mainly from the sticking and fusion of particles."

Jan 1, 2011

By Ruixiang Wang, Jinhui Li, Youjun Xiao, Daoling Xiong, Hao Chen

"Leaching solution prepared from spent battery materials contains large quantities of valuable metals, such as Cu, Ni, Co, Mn and Fe. Therefore, recovery of valuable metals from acidic polymetallic aqueous solutions is of great importance for every plant. In this work, a method is introduced of recovery of Ni, Co and Mn from polymetallic solution prepared by leaching spent battery material. The basic concept includes copper was removed through replacement by iron powder followed by iron precipitation in goethite method. The experimental results show that Cu can be removed 99% at least through replacement by Fe powder, and the removal of Fe can achieve 99% by goethite method. At the same time, the loss of Ni, Co and Mn are about 2%, 3 % and 2%, respectively. The process of differential removal of metals can be selected as the treatment alternative that combines simplicity, efficiency and reliability with low capital and maintenance costs. The purified solution which only contains Ni, Co and Mn can be used to prepare NixCoyMnz ternary system precursor.1 IntroductionNickel and Cobalt are very important metals which are applied in many fields, such as energy material and support material for some new material field. The world demands for such metals is progressively increasing, while raw resources are being depleted and with the constraints raised by the Law and related legislation assigned to protect the environment from hazardous wastes in the world. Nowadays study on reutilization of waste materials has great significance for achieving secondary resources recycling and preventing environmental pollution. There are many hydrometallurgy methods applied for dealing with these wastes, while they usually contain large quantities of valuable metals, such as Cu, Co, Mn and Ni, as well as impurities, such as Fe, Zn, and etc. Therefore, proper treatment of these leaching solutions prior to their discharge is of great importance, so that the contained valuable metals can be recovered.Separation and extraction of metals from leaching solution can use some methods through solvent extraction[l,2], ion exchange[3,4], precipitation with sulfide[ 5] or alkali[ 6] and electrolytic recovery[?]. Among the appropriate treatment alternatives, replacement and differential precipitation is the most attractive treatment that combines simplicity, efficiency and reliability with low capital and maintenance costs."

Jan 1, 2011