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By Hector M. Henao

There is an increasing trend in the copper smelters to recycle electronic materials, which contain relatively high concentration of precious metals. As a consequence, the amount of precious metals lost in the slag phase is increasing. To determine the portion of the precious metals chemically dissolved and that associated with the mechanically trapped matte in the slag will be a key factor to improve the recovery of those metals. Thus, an experimental study was carried out to determine the distribution of precious metals (Au, Pt, Pd, Rh, Ru) between the equilibrated copper matte and iron-silicate slag phases. The experiments were made in a magnesia crucible at 1573 K and a fixed partial pressure of SO2 of 0.1 atm for the matte grades between 40 and 70 mass% of copper. It was found that the distribution ratios (defined as mass% X in slag/mass% X in matte, where X represents the precious metal) are around 10-2 for Ru, 10-3 for Au, Pt and Pd and 10-4 for Rh. The distribution ratios show a tendency to increase when the grade of matte is increased.

Jan 1, 2006

By Daniel Kim, Justin McAllister, Shijie Wang

"At the Kennecott Utah Copper Refinery, impurities in the electrolyte are being precipitated in the circulation system and form a hard scale in the piping. This scale must be removed periodically for proper electrolyte flow. Distinct layers of differing composition form as the operating conditions of the tank house change. Scale samples from the inlet and outlet pipes were analyzed to discover the nature of the precipitates. Each sample was sectioned and examined under optical microscopy and SEM. The composition of the scale was analyzed using ICP, XRD, and SEM/EDX mapping. The rate of deposition was determined by measuring the amount deposited on new pipes after elapsed time intervals. In order to determine how to minimize the formation of the scale, the mechanism was studied and the results are presented in this paper.IntroductionIn copper electrorefining, impure copper anodes are refined into pure copper cathodes. The impurities from the anodes are either insoluble and report to the slimes or soluble and dissolve concentrating in the electrolyte. These impurities are controlled by bleeding electrolyte from the system. Over time, the impurities combine to precipitate a hard scale on the surfaces contacted by the electrolyte. The scale causes problems with tank house circulation systems. In order for the refinery to operate properly, the scale must be removed periodically from the walls of the pipes. The first step to control the buildup of scale on the pipes is to understand the composition and the phases that are present in the scale."

Jan 1, 2012

By Wellington Pereira Inácio, Frederico Muylaert Margem, Artur Camposo Pereira, Sergio Neves

"Natural fibers are currently gaining attention as reinforcement of polymer composites for uses in engineering parts for automobile and building construction. In spite of environmental, economical and societal advantages, the natural lignocellulosic fibers are not as uniform in their dimension and properties as compared to synthetic. In recent works it was found that the variation in strength could be correlate to the equivalent diameters for several lignocellulosic fibers including the sisal fibers. In the present work an investigation on a possible correlation of the equivalent diameter with changes in density and elastic modulus was carried out. Precise measurements of the equivalent diameter, conducted in a profile projector, were correlated with the density and the elastic modulus by means of the Weibull statistic analysis. The results showed that an inverse correlation with the diameter also applies for both the density and the elastic modulus with a high degree of precision. SEM observation of the sisal fiber in structure and fracture aspects strongly indicate that defects and microfibril participation could be responsible for the inverse correlation.IntroductionAccording to Kalia [1], cellulose-based fibers are currently being pushed owing to their ""green"" image. Contrary to synthetic glass fiber, extensively used in our modem technology, these lignocellulosic fibers are renewable and can be incinerated at the end of the material's lifetime without adding pollution in the atmosphere moreover, the amount of CO2 released during incineration process is negligible as compared to the corresponding amount taken up by the plant throughout its lifetime. Even if an industrial processing equivalent of C02 release is added, the lignocellulosic fiber is considered neutral with respect to the emission of gases responsible for the global warming [2]."

Jan 1, 2012

By Tianyou Huang, Yuan Lu, Haimin Long, Jinwu Kang, Gang Nie

"The distortion of metal parts during heat treatment process is one of the main obstacles in industry to ensure high-quality work and less or no machining allowance, especially for large but thin steel castings such as heavy turbine blades. In the paper, a method is proposed to control the distortion by adjusting heat transfer coefficient of metal parts during heat treatment process. Required heat transfer coefficients can be realized by getting the metal parts into contact with various media such as water spray, insulation felt or materials with different heat conductivity. The control method based on this idea is set up and achieved. By using insulation felt and water spray to change the heat transfer coefficient during the stages of heat treatment process, the results indicate that the proper control time and vary with materials.IntroductionThe distortion of metal parts during heat treatment process is one of the main obstacles in industry to ensure high-quality work and to realize less or no machining allowance [1]. For example, the Three Gorges turbine blade’s distortion is as large as 50mm during heat treatment process. The uneven heating and cooling during heat treatment process is the main reason for distortion [2]. By adjusting heat transfer coefficient of different areas of metal parts, the heat treatment process could be controlled. The temperature variation, direct cause for distortion, could be under control. Loeser Klaus used high pressure gas to achieve uniform heat transfer during gas quenching and proposed the possibility to use ""Dynamic Quenching"" processes where the quenching severity is varied during quenching by stepwise control of either gas velocity or gas pressure [3]. Li Zhichao also suggested minimizing distortion by marking a component into several areas and imposing different heat transfer coefficients on each area [4]. Heat transfer coefficient can be controlled by getting the metal parts into contact with different media such as water spray, insulation felt, air or different heat conduction materials. In addition, the exact time to adjust the heat transfer coefficient is another factor for distortion. A method is presented in this paper by actively adjusting heat transfer coefficient for different areas of metal parts and different stages of heat treatment process to control their distortion. The corresponding experiments have been made by using different metal materials."

Jan 1, 2012

By K. Verbeken, E. Wettinck, M. Verhaege

Iron (III) can easily and selectively be removed from acidic sulphate solutions with organo-phosphoric acids like Di-2-Ethyl-Hexyl-Phosphoric Acid [D2EHPA]. Stripping of the iron (III) loaded organic, however, is difficult unless highly concentrated inorganic acid solutions are used. In this paper results are shown for the enhanced stripping of iron from loaded D2EHPA by electro-reduction. The loaded solvent is contacted with a 2 M H2SO4 solution, which is continuously recycled in an electrochemical reactor where iron (III) is reduced to iron(II). As iron (II) is not extracted by D2EHPA, the equilibrium for iron (III)- D2EHPA is shifted towards the aqueous iron (Il)-sulphuric acid solution. The electro-reduction unit is a vessel with separated catholyte and anolyte chambers. The catholyte is the actual stripping solution where iron (III) is reduced to iron (II) on a stainless steel electrode. The anolyte is a 2 M H2SO4 solution where oxygen is evolved on a lead alloy electrode. A sintered glass plug separates the compartments. With this unit, enhanced stripping of iron from the solvent is possible under mild acid conditions [2 M H2SO4], and a concentrated ferrous sulphate solution can be obtained. The results shown have mainly been obtained by studying the parameters affecting the electro-reductive stripping of a D2EHPA loaded organic phase in a batch reactor. From an iron (IH)-saturated 20 vol. % D2EHPA solvent containing ~ 12.5 g/1 Fe (III) over 90% of the iron can be stripped in one stage with a 2 M H2SO4 solution at 50°C. It is shown that in this way it should be possible to obtain a concentrated ferrous sulphate solution which can be processed downstream to recover a pure iron product.

Jan 1, 2000

By Gavin K. W. Freeman

The efficient separation of cobalt from nickel is a fundamental objective in the refining of cobalt. Based on recent experience at the Corefco refinery in Fort Saskatchewan, the identification of a novel process for the selective precipitation of cobalt from aqueous ammonia leach liquors is described. The addition of calcium sulphate, CaSO4.2H2O (gypsum), to an aqueous solution containing cobalt(III) hexammine sulphate, [Co(NH3)6]2(SO4)3, will result in the precipitation of a sparingly soluble double salt having the stoichiometry, [Co(NH3)6]2(SO4)3.2CaSO4.xH2O, where x = 4 or 6. Leach residues, which may contain a significant quantity of cobalt associated with the cobalt calcium double salt, can be washed with process solutions that contain ammonium carbonate. After contact with ammonium carbonate, the cobalt is recovered into solution, while the calcium is re-precipitated as the insoluble carbonate. The simplicity of this elemental separation and its high selectivity for cobalt, as well as the demonstrated usefulness in improving cobalt recoveries, are the basis for the potential applications of this process.

Jan 1, 2003

By Lanre Oshinowo

The trend in process engineering is to design compact, more efficient processes, there is the paramount requirement to get the job done right the first time going from the drawing board to full-scale commercial operation. To accomplish this goal, there is also the need for tools beyond the traditional engineering toolkit to evaluate designs through virtual prototyping, thereby reducing the risks associated with making design decisions. One of the most important tools that has recently come to the forefront of process design and development is Computational Fluid Dynamics (CFD). CFD has been used at HATCH to address the key process parameters that drive the design of hydrometallurgical unit operations. This paper will detail the role of CFD at HATCH in achieving a superior level of confidence in the process design of autoclave circuits. Specifically, the optimum application of multiphase modeling including hydrodynamic, heat and mass transfer to hydrometallurgy operations, the impact of non-Newtonian slurry rheology on autoclave performance, and the challenges of optimizing the mixing of key reactants into slurries in autoclave reactors, is discussed.

Jan 1, 2003

By S. J. Kohut

Until recently SX-EW technology has only been used to produce conventional cathode for the cyclical commodity marketplace. Unlike electrorefining, SX-EW lends itself to the integration with the downstream manufacturing technologies for direct mine site production of value added products. The integration of SX-EW and downstream manufacturing results in the elimination of redundant process steps, the cost savings, and the access to value added product markets which can buffer the producer from swings in the cathode market. SX-EW production of copper powder and powder-based products has been demonstrated at the pilot plant level. The SX-EW process has been successfully redesigned to meet the more specific demands of engineered products. Challenges include the solution purity, the cell ventilation, the high current density operation and the product handling. Successful demonstration of mine site production of value added SX- EW products opens up new non-commodity marketplaces to the mining industry.

Jan 1, 1999

By P. Chris Pistorius

Calcium treatment of alumina inclusions, to convert the alumina to molten or partially molten calcium aluminates, is a well-established treatment for steel, to improve the castability of aluminium-killed steel. However, the role of magnesium in calcium-treated steel is not fully clear, nor is the origin of the several percent of magnesium oxide that is often present in calcium-treated inclusions. To study this, steel was sampled after calcium treatment at an industrial steel plant, and the inclusions identified by energy-dispersive X-ray microanalysis (EDX) on polished sections of the samples (analysing the samples in a scanning electron microscope). The predicted fraction liquid in the inclusion was estimated from the ternary alumina-magnesia-lime phase diagram. Inclusions with higher CaO contents generally had lower MgO contents, indicating that the calcium wire is not the origin of the magnesium in the inclusions; this was also confirmed by wet chemical analysis of the calcium wire. Instead, it appears that magnesium-alumina spinel inclusions form during extended ladle contact after aluminium killing and before calcium treatment. While such spinels have been stated to cause poor castability (clogging the submerged-entry nozzle), it is clear that calcium treatment successfully modifies the spinel inclusions to mixed alumina-lime-magnesia inclusions, where the magnesia content contributes substantially to liquefaction of the inclusions: for typical MgO contents of around 10%, the range of Ca:O ratios which yield liquid (or partially liquid) inclusions is extended substantially to lower Ca:O ratios.

Jan 1, 2006

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

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

Jan 1, 2008

By R. D. Prengaman

Lead usage in paint, anti-knock gasoline additives, pipes, seals, and solder has declined markedly over the past 30 years. Products utilizing the unique properties of lead and its ability to be recycled have survived and grown. These products include shielding, glass (particularly TV and computer screens), sheet for roofing, stabilizers for PVC, insoluble anodes for metal production, electronic solders and lead acid batteries. With the loss of markets many companies have decreased lead product development efforts. Much of the patent lead materials development is devoted to lead acid batteries. In the past 25 years, the automobile battery has been almost doubled in power and reduced in weight, leading to a nearly three-fold increase in performance. Corrosion-resistant lead alloys and improved battery designs have made battery lead usage more efficient. The same corrosion-resistant battery alloys are utilized to increase the life of electrowinning anodes. The challenge for lead product development is not only to maintain and improve the existing lead products, but also to develop the growing lead acid battery market for telecommunications, uninterruptive power sources, remote area power, hybrid and electric vehicles. Lead

Jan 1, 2000

Iron(II), sulphur dioxide and sugars such as lactose are potential reducing agents for manganese dioxide to produce manganese(II) for subsequent hydrometallurgical treatment. The leaching of limonitic laterite and manganiferrous ores with sulphur dioxide produces iron(II) which in turn can catalyse the leaching of manganese dioxide in acid media. This paper presents a critical analysis of the kinetics of reductive dissolution of synthetic manganese dioxide and manganese ore to compare and contrast the effect of sulphur dioxide and iron(II) in acid media containing sulphate or perchlorate anions. Both one-electron and two-electron mechanisms are considered in the case of sulphur dioxide. The current knowledge on chemical speciation is used to construct an Eh-pH diagram to show the effect of complexation of Mn(II), Fe(II) and Fe(III) with sulphate. Heterogeneous and electrochemical reaction kinetic models are combined to propose reaction mechanisms which rationalize the dissolution kinetics.

Jan 1, 2003

By R. Parada

In January 1995, Disputada Mining Company Ltd. (Compañia Minera Disputada de Las Condes) started up the Expansion Project for the Chagres Smelter, following an investment of US$M 2 15. The new smelter replaced the 44,000 tomes per year revervatory furnace with an Outokumpu Flash Smelting Furnace (FSF) designed to produce 118,000 tonnes per year of copper. Nowadays, this smelting unit has achieved a 40% over design performance. The landmarks of this modernization project are described. The start up period in 1995-1996 was characterized by the impacts of several restrictions that prevented the smelter from reach design production. The design performance was reached in 1997-1998 through the implementation of solutions designed to eliminate, or at least mitigate, the restrictions found early on. The smelter has been further optimized in the 1999-2000 period, leading to a new record anode copper production rate of 148,000 tonnes in 2000 while obtaining 98% approval for our different anode shapes. The objective of this paper is to discuss the consecutive processes of start-up, achievement of design capacity, and operational improvements to go well beyond the design capacity. These processes took place between early 1995 and late 2000, under the principles of Continuous Improvement that promotes the effective participation of the workers in the technology innovation and Enterprise Management.

Jan 1, 2002

By Osamu Yamamoto

In antibacterial evaluation of carbon-ceramic composites, we prepared two type composites with emphasis on carbon-ZnO system; one was porous carbon materials containing ZnO nano-particles and another was porous ZnO coated with carbon thin film. Porous carbon samples containing ZnO at highly dispersed state were prepared by carbonizing the resin exchanged by Zn2+ ion. Porous ZnO coated with carbon thin film was obtained by the pyrolysis of poly (vinyl alcohol). Antibacterial activity of these composites obtained was evaluated by measuring the changes in electrical conductivity with bacteria growth. The antibacterial activity on the composites increased with the increase of t he amount of ZnO in composite and decreased with the increase of carbonization temperature. The antibacterial activity for Staphylococcus aureuswas found to be stronger than that for Escherichia coli. No activity of the carbon samples without ZnO was observed. The occurrence of antibacterial activity was supposed to be due to the generation of hydrogen peroxide from ZnO in composite. In the present work, antibacterial activity of carbon-ZnO composites was studied in the details.

Jan 1, 2006

By M. E. Ramos Rada

Mexicana de Cobre, which is part of Grupo Mexico, carried out studies for the construction of a copper refinery in the La Caridad Metallurgical Complex located in Nacozari, in the state of Sonora, Mexico. After the studies were concluded, the decision was made to construct a 180,000 t/y refinery using the state of the art permanent cathode Kidd Process. The basic engineering was developed by Fluor Daniel and the detail engineering and the construction were carried out in record time by the Mexican company Bufete Industrial. During the construction phase, Grupo Mexico decided to expand the refinery, and actions were taken to increase its capacity by an additional 120,000 t/y; the final result was a refinery capable of producing 300,000 tonnes of grade A cathode per year. Construction began in January 1996, and the operation of the first stage began on July 1, 1997. The operation of the second stage commenced on January 7, 1998. The capacity of the first stage was reached in November, 1997 and the total capacity of the refinery was achieved in May, 1998. This presentation describes the process and equipment installed in the refinery, the steps leading to the start-up, the operation and the results obtained during the first two years, the handling of anodes with high impurity contents, and the problems confronted and the way they have been solved. It also includes personnel productivity, the control parameters and the most relevant data on the operation of the process.

Jan 1, 1999

By R. Togashi, S. Kuramochi, T. Yamada

In 1972, the Akita Zinc Co., Ltd. commenced operations with an annual capacity of 86,000 tonnes of electrolytic zinc, and it has operated with an annual capacity of 156,000 t-Zn since 1974. The business surroundings for non-ferrous metals production have become more severe with the high Yen rate for the dollar and low domestic demand in the last few years. Consequently, the company tried to survive with some improvements and succeeded to reduce operating costs and to improve profitability as follows: 1) expansion of its production capacity to. 196,000 t-Zn annually, 2) saving man-power by the introduction of fully-automated machines for cathode handling in the cellhouse, 3) improvement of the hematite process by means of the recovery of rare-metals. These improvements made Akita Zinc a competitive refinery in the modern world. We have been trying to improve the operations more and more. One of the challenges is to purify the iron oxide made in the hematite process by applying an As removal process, which is coming into operation in the near future.

Jan 1, 2000

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

By Jiangtao Li, Zhongwei Zhao, Xingyu Chen, Xuheng Liu

The method of ultrasonic-assisted leaching was used to extract vanadium from the stone coal, with alkali as leaching reagent. The effects of ultrasonic power, concentration of alkali, reaction temperature, liquid-solid ratio and reaction time were investigated, respectively. The optimal ultrasonic leaching condition for vanadium extraction is as follows: ultrasonic power 230W, concentration of alkali 5%, liquid-solid ratio 3:1, reaction temperature 90℃ and reaction time 1h. The leaching rate of vanadium reaches 76.4% under the optimal condition, which is 12.2% higher than that of non-ultrasonic leaching. The reason on enhancing the leaching rate of vanadium by ultrasonic leaching was discussed. It is indicated that the ultrasonic cavitation can increase the surface area of mineral, which is beneficial to facilitate the reaction rate. Keywords: stone coal; vanadium; alkaline leaching; ultrasonic

Jan 1, 2014

By Dirce H. Jacomo, Jaciele G. Teixeira, Anibal Y. Abreu Castillo, EsperidianaA. B. Moura, Yalquiria A. Silva, Rene R. Oliveira, Michelle G. Gomes

"Composites consisting of poly(vinyl alcohol), starch and sugarcane bagasse ashes, using glycerol as plasticizer agent, were prepared by solution casting method. Composites prepared were subjected to electron-beam radiation treatments, at radiation dose of 50 and 80 kGy using a Dynamitron electron beam accelerator, at room temperature in the presence of air. The composite samples obtained were evaluated for their water absorption, mechanical and morphological properties.1. IntroductionThe potential of biodegradable polymers and more specifically of biocomposites obtained from agro-resources have long been well established [1-3]. Starch, derivate from variety of botanical sources (cereals, legumes, and tubers) is widely available raw material and one of the most studied and promising agro-resources for the production of biodegradable polymers as matrices for biocomposite applications. However, starch itself is very brittle, hydrophilic and its mechanical properties are very poor for many applications [3 - 5]. The blending of starch with conventional polymers is a promising approach to improve its drawbacks. Recently, many efforts have been made to blend starch with biodegradable synthetic polymers [5, 6]. Polyvinyl alcohol (PYA) is a particularly well-suited synthetic polymer for the formulation of blends with natural polymers, as it is highly polar and can also be manipulated in water solutions, and depending upon its grade, in functional organic solvents as well [3, 7]. PY A has been reported to be an option to blend with starch. Most of the starch/PY A composites have been prepared by casting. However, it is well known that starch/PY A composites has poor in water resistance and mechanical properties after absorbing water [3,8]. Attempts to improve the mechanical properties and to decrease the water absorption property of the starch/PY A composites are made by adding the cross-linkers and plasticizers. Park et al. prepared starch/PY A/citric acid films by the casting method. They also studied the effect of (spell out) citric acid on the mechanical properties and water resistance of composites [9]. Zhai et al. prepared the starch/PY A hydrogels using electron-beam radiation [10]. Different kinds of lignocellulosic fibers have been investigated in blends for formulation of biocomposites."

Jan 1, 2013

By Martín Reyes

Iron concentration by ion flotation techniques, from sulfate solutions in presence of zinc was studied in a laboratory flotation column by continuous mode using a synthesized sand shell plate sparger, an anionic collector, promoters, and surfactant propylenglicol 400. Effects of experimental parameters, such as the concentration of reagent: potassium amyl xanthate and dithiophosphate, superficial gas velocity, and superficial liquid velocity were studied in terms of the recovery and enrichment of Fe (III). The results show that the iron elimination from the solution in the presence and absence of zinc (II) are of 59 % and 72 % respectively. The flotation efficiencies decrease with an increase of the concentration of xanthate and air flow rate. The best recovery was achieved, at Jg 0.1 cm/s, Jl 0.72 cm/s and a mixture of xanthate and dithiophosphate as promoter. It was also demonstrated that it is possible to selectively separate and concentrate iron (III) from solutions containing zinc. The behavior of iron ion flotation in a flotation column is reported in this research as a gas hold up, superficial gas velocity, bubble size and superficial bubbles area flux function. The results show that the extraction of aqueous ions of metal iron by ion flotation is strongly affected by: [C], Jg (cm/s), eg (%), Db (mm), Jl (cm/s), y Sb (s-1).

Jan 1, 2009