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By Ximena Diaz

Mercury is one of the most undesirable contaminants in gold bearing ores. During cyanidation mercury cyanide compounds accompany gold in all the extraction and recovery processes. Of course mercury in the carbon eluates creates environmental problems in subsequent refining steps. One possible process alternative for the separation of gold from mercury in such concentrated alkaline cyanide solutions is the selective solvent extraction of gold by undiluted Dibutyl Butyl Phosphonate (DBBP). In order to describe the behavior of mercury during extraction by DBBP, the results from a preliminary research program are presented. In this study, temperature and cyanide concentration have been found to be the most significant variables which influence the separation of gold from mercury by solvent extraction using DBBP. It was found, using plant eluate from a carbon strip, that excellent separation of gold from mercury can be obtained at 60' C with 98% gold recovery and complete mercury rejection in a single stage of extraction. The influence of pH is also discussed in terms of the extraction chemistry. These results complement previous research which described the DBBP solvation extraction of an aurocyanide ion pair. In addition, these results extend our understanding of the alkyl phosphorous ester extraction systems by illustrating that neutral ionic species such as Hg(cN)02sq, can be extracted at low cyanide concentrations, a phenomenon which had not been observed previously for other cyanoanions.

Jan 1, 1993

By E. García-Ramos, P. Flores-Sánchez, E. G. Palacios, B. Zeifert, A. Romero-Serrano, M. Hallen-López

Chromium containing slags from stainless steelmaking may eventually be leached by acidic environments, therefore they should be treated before being stockpiled or land filled. In this work, synthetic slags were prepared and the effect of CaO/SiO2, Cr2O3, MgO and Al2O3 contents on the stability of the mineralogical species formed was analyzed. The morphology and composition of the slags were analyzed by XRD and SEM-EDS, whilst their chemical stability was evaluated by leaching with an aqueous acetic acid solution. It was found that CaCr2O4 and CaCrO4 are present in slags prepared with neither MgO nor Al2O3. The Al2O3-based slags mainly produced Ca2Al2SiO7 and the Cr(VI)-containing oxide complex Ca4Al6CrO16, whilst MgO-based slags produced MgCr2O4 as main mineralogical species. Additionally, Eh-pH diagrams for the Ca-Cr-H2O and Mg-Cr-H2O systems at 25 °C were constructed. The lowest Cr concentration levels in the leaching liquors corresponded to MgO-based slags owing to the stable binding of Cr in spinel with MgO. It was also observed in the Al2O3-based slags that increasing the slag basicity from 1 to 2 the leachability of the slags are notably increased.

Jan 1, 2008

By A. Erçin Ersundu

In the present work, three different domestic iron ores; Sivas Divrigi B Head high grade hematite lump ore, Malatya-Hekimhan-Hasançelebi medium and low grade magnetite lump ores reduced with Soma-Kisrakdere lignite coal to investigate their suitability for sponge iron production. A laboratory scale box furnace was used to carry out the reduction experiments. In the experimental studies different operation parameters were selected being Cfix/Fetot. ratio, temperature in the range of 1100 - 1250 oC and time, to determine their effects on metallization. Metallization degree up to 90 % was found in the reduction experiments realized by using Sivas Divrigi B Head high grade hematite lump ore, whereas for Malatya-Hekimhan-Hasançelebi medium and low grade magnetite lump ores 60 - 65 % metallization degrees were obtained.

Jan 1, 2008

By James C. Sever

Two green field magnesium reduction plants are under consideration using dolomite as the raw material. The Calix calciner was independently selected for both plants. The unique design of this calciner is detailed and the advantages defined for the specific application. The low carbon foot print of this unit combined with the ability to capture food grade carbon dioxide makes this an environmentally proactive approach to carboniferous ore calcination.

Jan 1, 2015

By Merete Tangstad, Eli Ringdalen

"In Norway ferrosilicon/silicon and ferromanganese production are strong with world markets of 4 % / 9 % and 4 %, respectively. Research and development in the academia mirrors the national interest; hence, there has been extensive academic research in these areas. There are some vital drivers and premises for a successful cooperation between the academia and industry with the main driver being a win-win situation for both. For industry,the potential advantages include cost-, competence- or environmental- benefits; for academia, the important drivers are building of competence and equipment, educating more students at higher levels, and increased possibilities to publish. In Norway, the benefits of cooperation between industry and academia are basic knowledge regarding thermodynamic and kinetic data, as well as reaction mechanisms within core processes. In recent years, such research interests have focused on the depletion of raw materials as well as environmental issues.IntroductionIn 1989, the Norwegian Ferroalloy Producers Research Association (FFF) was funded on the belief that a common research association would benefit the industry by making it easier to perform basic research as well as paving the ground for better recruitment to the industry. The funding partners in Norway were the FeSi/Si and FeMn producers. Today, the producers are Elkem, Finnfjord, Fesil, Wacker, Eramet and Vale. The main research partners working with FFF are SINTEF (Materials and Chemistry) and the Department of Material Science and Engineering at the Norwegian University of Science and Technology (NTNU). With more than 1700 employees, SINTEF is the largest independent research organization in Norway and NTNU is the largest technical university. Together, the two organizations provide an exceptionally strong materials technology research environment, and especially so for pyrometallurgical research."

Jan 1, 2012

By R. N. O'Brien, E. Peters

"It has been discovered that copper concentrates can be leached in strong (40-60%) sulfuric acid with nitric acid, or with oxygen if nitric acid is present as a catalyst. Chalcopyrite is rapidly decomposed at temperatures well below the boiling temperature of the lixiviant (-150 C.) and the resulting copper and ferric salts are precipitated as CuS04.H20 and FeH(S04)z.4H20. Other metal sulfides such as zinc, lead, nickel, etc. are also converted to sulfates that are nearly insoluble. Sulfur is partially converted to elemental and partially to sulfuric acid. Reduction products of nitric acid can be recovered from the distillate with good recovery. Conversion of as-received copper concentrates is largely complete in about 1 hour. Introduction9 molar sulfuric acid is an unusual hydrometallurgical lixiviant: it has a boiling point of about 150 C. and a low solubility for base metal sulfates. Below about 6 molar acid, the boiling point falls below 120 C. and yields much higher sulfate salt solubility, while above 12 or 13 molar acid and at higher temperature sulfuric acid becomes an oxidizing agent, yielding gaseous S02' Thus, sulfuric acid within this range of concentration is capable of acting well above the temperature of boiling water without requiring autoclave conditions, and if typical oxidative leaching conditions are applied to suspended mineral sulfide concentrates, it is possible to obtain a conversion of these sulfides into 'crystalline sulfates. Thereafter, the sulfates can be separated by filtration or by solid - bowl centrifuge and the solution can be recirculated to the reactor vessel. Meanwhile, the solid sulfates can be treated in a typical hydrometallurgical circuit, i.e., dissolved in a return stream that is essentially water, separated from each other by, for example, solvent extraction, and recovered as metals by electrowinning."

Jan 1, 1997

By Biswadeep Saha, Meenakshisundaram Ramanathan, Chai Ren, Sivaraman Guruswamy

"Fe-Ga alloys have a large low-field magnetostriction and these alloys are attractive candidates in energy conversion and harvesting applications. Small additions of W also increase the magnetostriction of Fe. In this paper changes in magnetostriction by W substitution for Ga in various Fe-x at.% Ga alloys are presented. Fe-Ga-W single crystals were grown using vertical Bridgman Growth technique. [001]-orientated single crystal samples were prepared with faces within 1 degree off <100> orientation. The samples were annealed at 1150 °C in the alpha-phase region and water quenched. The magnetostriction coefficient (3/2)A-100 measurements were made on these Fe-Ga-W single crystals. The result on the effects of W substitution and annealing on the magnetostrictive behavior of these alloys are discussed.*Support of this work by NSF-DMR under the award DMR-0854166 is gratefully acknowledged.IntroductionMagnetostrictive materials changes their dimension exhibit reversible strains and changes in elastic properties in the presence of an applied magnetic field or the reciprocal effect of changes in the magnetic properties with the application of stress [IJ and are very important in sensor, actuator device, linear motor, magnetomechanical devices, microelectro- mechanical devices, active vibration dampening devices application areas. The discovery of an order of magnitude enhancement in the magnetostriction of Fe with Ga addition coupled with low saturation magnetic fields, and excellent mechanical properties opened up the possibility of obtaining larger magnetostriction values in other low-cost ductile a-Fe phase based alloys with alloying additives that are less expensive than rareearths such as Tb and Dy [2·4l_ The magnetostriction values observed in Fe-Ga single crystals are sensitive to thermal history and composition. The formation of second short range ordering phases and local defects inside crystal structure can also cause a dramatic change to this alloy's magnetostriction behavior [5-9l_"

Jan 1, 2012

By Takayuki Watanabe, Yoshiki Shimizu, Yusuke Moriyoshi

"B-C-N nanotubes prepared by a flush evaporation method using a de arc plasma were mainly characterized by transmission electron microscopy (TEM) and electron energy· loss spectroscopy (EELS). The nanotubes obtained· were divided into three types such as carbon boron nitride and carbon or carbon nanotubes surrounded with boron nitride nanotubes. These types of nanotubes were obtained at higher temperatures than about 3000 K, however, these were not formed at lower temperatures than about 3000K. On the other hand, 11anocapsules were· formed at all the experimental temperatures and nanocapsules with a homogeneous phase were obtained at lower temperatures than about 3000 K. The effect of additives on the formation of B-C-N nanotubes was not clear. Based on these experimental data depending on temperatures and corresponding microstructures, the formation mechanisms of both nanotubes and nanocapsules were briefly .discussed 1 Introduction As reported previously, nano tubes have unique electrical properties1, 3) The preparations of nallotupes have been usually carried out by flush evaporation methods using either a de arc plasma or a laser4 -5) By these methods the reaction rate is so rarid that we have no data of intermediate products between initial raw materials and. final products of nanotubes 6-9). So, the formation mechanisms of nanotubes have been mainly speculated only from the microstructures of resultant nanoiubes. In order to have more reliable formation mechanisms, it is particularly important to have the information of intermediate products at the corresponding temperatures. From the viewpoints, we have studied about the effects of temperatures on the preparation of nanolubes. Here we report mi firstly some problems on the preparation of B-C-N nanotubes 10), secondly the effects of temperatures on the preparation of B-C-N nanotubes, and finally the formation mechanisms of nanotubes."

Jan 1, 2000

By Xuyang Liu, Xuewei Lv, Chenguang Bai, Meilong Hu

"The electro-deoxidation process for ilmenite concentrate in molten salt was studied by cyclic voltammetry and AC impedance spectroscopy. The results from cyclic voltammetry are consistent with those of AC impedance spectroscopy. The results showed that the electro-deoxidation process for ilmenite concentrate consists of two steps. In the first step, Fe is reduced from the ilmenite concentrate. The second reaction is the decomposition of TiCh. CaTiCh is an intermediate product. At low voltage, the electrochemical reaction is the main step. With the increasing potential, the diffusion of ion is the main rate controlling step for the electro-deoxidation of FeTiO3.IntroductionTitania and titanium-rich products are mainly prepared from ilmenite concentrates (FeTi03), which contain about 40%-60% T1O2 after ore dressing and other physical or chemical processes [1]. At present, the main methods to prepare titania are the sulfuric acid process and the chloride process, but the sulfuric acid process consumes a large amount of sulfuric acid and the materials requirements for the chloride process are strict [2], Since the Electro-Deoxidization in Molten Salt (FFC) method was put forward in 2000, many researchers have successfully extracted the metal and alloys by this method, such as Ti, Cr, Tb, Si, Al-Si, TiV, FeTi, etc. [3-7], FeTi alloy is a typical hydrogen storage material, and because of its favorable properties, the preparation of FeTi alloy has become a hot research topic [7-9]. However, the mechanism of electro-deoxidization has not been studied thoroughly [10-11]. Therefore, in this study, the electro-deoxidation process for titanium concentrate was investigated by electrochemical methods, and the study makes a contribution to improving the current efficiency of the electrolysis."

Jan 1, 2012

By John R. Howell

"SUMMARYThe process of producing a new cast component requires significant design and development by both the design engineer and the foundry engineer. This effort strives to produce a high quality component at minimum cost. To assist in this development, an analysis system, consisting of several computer programs, has been developed to simulate the metal casting process. This system incorporates analytical geometric solid modeling, finite element analysis, results display, and an innovative technique to model the casting mold with surface boundary conditions.The simulation has produced excellent thermal results and work is in progress to develop techniques to enable use of this data in additional analyses to predict porosity and residual stress. Research is required to produce working parametric formulations of material properties. Software development is required to develop good fluid flow analyses for large. 3D models to simulate filling of and convection in molds.Integrating this system of programs is difficult due to proprietary database structures used by software developers. However, an acceptable means has been accomplished' to move data from one program to another. Further software development is required to facilitate this task. INTRODUCTIONThe process of producing a new cast component requires significant design and development by both the design and foundry engineer. This effort strives to produce a high quality, reliable component at minimum cost in a timely manner. The design engineer needs to know the physical and mechanical properites which can be expected in the actual part at critical areas. This will enable him to design a part with minimum material while fulfilling the performance required. The foundry engineer needs to produce a sound, quality casting with a minimal amount of material In risers, the feeding system and machining stock. This must be done with a minimum· investment in tooling and development time and maximum productivity of labor and capital employed. This task Is continually being made more difficult because of increased competition in the marketplace and the use of castings in more severe service. This has strongly influenced the need for high quality castings.The task of developing a new casting is difficult for both the design and foundry engineer. To assist in this development, Deere & Company has been engaged in the development of an analysis system to simulate material processes. A major portion of this program involves simulation of the metal casting process. This analysis system has evolved into a package of computer programs which simulates casting solidification and subsequent cooling through the finite element method"

Jan 1, 1986

By Hongmin Zhu, Guihua Wang, Xiangsheng Wang

"The anode process of carbon electrode in fluoride melt was studied by voltammetry and chronoamperometry. Anode gases were analyzed by gas chromatography on-line during controlled-potential electrolysis. Two peaks were observed on the cyclic voltammograms. According to the results of gas chromatography, the first peak was corresponded to the discharge of residual oxide ions, with the formation of CO and CO2. Discharge of fluoride ions occurred at 4.1 V vs. Li+/Li, and leading to the anode effect. With the occurrence of anode effect, small amount of CF4 was detected. As the potential reached 4.5 V, CF4 and C2F6 gas evolution occurred, and the current increased to form the second peak.1.IntroductionIn the primary production of Aluminum and some rare earth metals like neodymium, a departure from normal cell operation known as anode effect results in the generation of perfluorocarbons (PFCs), which have high global warming potentials [1]. Owing to the pressure of environmental protection, considerable research has been carried out to clarify the mechanism of anode effect and PFC generation of industry and laboratory cells in the aluminum electrolysis system [2-9]. The common result on PFC generation is that the PFCs are emitted from Hall-Heroult cells only when they are on anode effect. In this article, we selected LiF, the main electrolyte for the neodymium electrolysis [10-11], to perform further investigation on the underlying kinetics of PFC generation and the nature of the reactions at the electrode.2. ExperimentalAll experiments were carried out in an alumina tube reactor, which was filled with high purity helium atmosphere. Spectrographic graphite crucibles were used, which played the dual role of molten fluoride container and the counter electrode. Lithium fluoride was analytical grade. The experiments were carried out at 900 °C."

Jan 1, 2011

By Matthew D. Andriese, Jiann-Yang Hwang, Zhiwei Peng

"It has been demonstrated that metallic-bearing minerals are physically liberated from host rock when exposed to microwave (MW) energy. The metallic minerals are iron sulfides and spinel oxide minerals contained in peridotite rock. Experimental evidence has shown ore particles readily couple with MW energy at 2.45 GHz, 1000 W resulting in rapid heating. Thermal stresses are generated by highly absorbing metallic-bearing minerals resulting in cracking and embrittlement of ore particles that assists in crushing and grinding processes. The liberated metallic-bearing minerals are shown to report to coarser size fractions as a result of MW exposure.IntroductionComminution of ore material during beneficiation is a large energy expenditure for the mineral processing industry. Crushing and grinding operations alone consume 50-70% amount of energy used in mineral processing [1]. Size reduction becomes increasingly difficult with decreasing particle size making grinding the most energy-intensive step of comminution. The aim of comminution is to maximize liberation of economically valuable minerals from the host rock [2]. Overall, the less material that needs to be handled, then grinded, to create a useful product for hydro/pyro metallurgical processes will achieve the greatest reduction of energy.Much of the scientific interest for use of microwave (MW) energy in mineral processing has been for improved hydro/pyro metallurgical techniques [3-6]. Early authors have employed MW energy for improved grinding of ore particles but most conclude the energy savings do not justify the energy input [7-9]. The effectiveness of MW assisted grinding is dependent on the ore mineralogy and the absorptive properties of minerals contained within it. Ore containing magnetic minerals should prove successful with MW assisted breakage from highly absorptive properties."

Jan 1, 2012

By K. S. Kawatra

In recent years, there have been several efforts to develop binder mixtures for iron ore pelletization. Some efforts have been fruitful, while others have encountered failure. For example, adding corn starch to bentonite is effective, while adding fly ash to bentonite is not. When binders are made with fly ash, a pozzolanic reaction occurs, but no such reaction occurs when bentonite and corn starch are used together. The authors analyzed which binders can be mixed, and which binders will succeed. The authors confirmed this analysis with several laboratory and plant studies. This paper presents this critical analysis, along with various combinations of binders for making Iron Ore Pellets.

By M. Mujahid, A. Maqsood, M. H. Asghar, K Iqbal

"Thin film multilayer anti-reflection coatings (Si02/Si/Si02) having thicknesses 286/571/143nm were deposited by RF magnetron sputtering deposition technique on 0.5mm thick Si(100)-substrates. Post-deposition annealing is also carried out in the temperature range 150-650°C for 4hr at the rate of 10°C /min. Si Optical window was designed at 4.21lm wavelengths and correlated with modeling software. The films are transparent in the 3-51lffi band of the electromagnetic spectrum, firmly adhered to the substrate. The prepared multilayer thin films are characterized optically and structurally using a spectrophotometer, an atomic force microscope, x-ray diffraction and a scanning electron microscope. Optical and structural characterizations show that the %transmittance is between 60% and 75%, no appreciable change in crystal structure and roughness of coatings vary between 9 and 25 nm when annealed in the temperature range of 150-650oC. Local elemental characterization on the surface of the thin film was carried out using energy dispersive spectroscopy. The quantitative result of energy dispersive spectroscopy has also shown that the ratio of Si to 0 on the film is 0.67: 1.IntroductionSi02 thin films have unique properties in the interfaces with Si and most studied materials in the field of microelectronics and optical devices [1]. Multilayer thin films are using nowadays in the design and fabrication of the shrinking systems with a variety of fields such as optoelectronic devices. The physical properties and parameters can be controlled at scales of microns down to nanometers by using RF magnetron sputtering system [2].Silicon and Silicon dioxide are used as coating materials [3]. These thin films are laid on top of each other in SiO2/Si/Si02 order by RF magnetron sputtering on top of a substrate as given in Table 1."

Jan 1, 2012

By Zhi-xiang Cui

Dongying Fangyuan Nonferrous Metals Co., Ltd. has developed a new technology to produce anode copper from concentrates through only two furnaces. This new technology is called the Two-Step Copper Smelting Process. This paper presents the commercial application of the Two-Step Copper Smelting Process and its operating conditions. The key features of the Fangyuan Two-Step Process are as follows: (1) feed materials, including concentrates and flux, are mixed without pretreatment and fed into the Submerged Lance Smelting (SLS) furnace; (2) high grade white metal (WM) produced by the SLS furnace is transferred via WM conduit into one of the two Submerged Lance Converting and Refining (SLCR) furnaces; and (3) the two SLCR furnaces blow alternatively to maintain continuous operation of the whole production chain. The new smelter started operation in October 2015 with a processing design capacity of 1.75 Mt/year of mixed feed and has been operating for over 30 months.

By Zachery Zanetell

Flotation circuit performance has become increasingly more challenging due to the complexity of available ore sources. To optimize value mineral recovery, the mineralogical composition of the ore should be evaluated and understood. Utilizing a variety of mineralogical and analytical tools, flotation processing challenges can be overcome and potential limitations understood. In this paper, several case studies will be discussed in terms of the value that has been provided through the use of mineralogical analysis to optimize flotation performance.

By JiaPeng Xu, Brian Lo, Uday B. Pal, Yihong Jiang, Soumendra N. Basu

"The Solid-Oxide Oxygen-Ion-Conducting Membrane (SOM) electrolysis process has been successfully tested on a laboratory scale, producing silicon directly from silica in a cost-effective and environmentally friendly way. A yttria-stabilized zirconia (YSZ) tube, closed at one end was employed to separate the molten salt containing dissolved silica from a liquid metal anode placed inside the YSZ tube. When the applied electric potential between the liquid tin cathode in the molten salt and the anode exceeds the dissociation potential of silica, oxygen ions are pumped out of the molten salt through the YSZ membrane and oxidized at the anode while the silicon cations in the flux are reduced to silicon at the liquid tin cathode. The presence of high-purity silicon crystals on the surface of liquid tin cathode was confirmed by scanning electron microscopy (SEM) and energy dispersive x-ray spectroscopy (EDS). Silicon crystals were extracted from tin cathode by chemical etching.IntroductionPhotovoltaics (PV) generate electrical power by using solar cells, and dramatically reduce the emissions of greenhouse gases (GHG). Through 2006 to 2011, it grew the fastest of all renewable technologies with operating capacity increasing an average of 58% annually [l]. However, the cost of manufacturing solar-grade silicon (SoG-Si) for high-efficiency solar energy production represents a major barrier to achieving the industrial goal for solar power of $1/Wp (watt at peak exposure) which would enable widespread grid parity. The current contract price of silicon to PV manufacturers is $50-$60/kg, with the spot market in 2007-2008 showing prices as high as $300/kg [2]. This makes the development of low cost and environmentally friendly manufacturing of high purity silicon very important."

Jan 1, 2013

By Y. Maeda

Non-ferrous smelting furnaces generally install a gas cooling system for treatment of waste gas containing SO2,. From the point of view of corrosion resistance and recovery of waste heat, the high pressure boiler system is the best way to cool gas, however this system requires high initial investment and relatively higher operating costs. Because the feasibility of this boiler system greatly depends on the smelting process and scale, other lower temperature systems, e.g. water-cooled jacket system, are more suitable if the smelting process does not produce enough steam nor generate enough electricity to compensate operating cost. In additton, the water-cooled jacket system is simple in structure and easy to operate. For those reasons, it is applied widely. A new smelting furnace was planned in our factory and it was necessary to install waste gas cooling equipment. In our case, a water-cooled jacket system was more feasible because of the low gas volume and high dust content. It was also expected to operate without maintenance for ten years. On the other hand, some leakage problems with the water-cooled jacket had been experienced in the past. That is because SO2 In the waste gas changed into sulfuric acid which corroded the jacket material. As the first step, several data from actual&apos; usage were reviewed to throw light on the corrosion process, and an appropriate procedure to determine the operating temperature of cooling water was obtained. For the basis of this study, a water-cooled jacket system was newly designed and tested for three months in a pilot plant. After this system&apos;s performance was confirmed, it was installed in a new furnace as a commercial plant. After one year of operation, the initial thickness of carbon steel jacket remains almost the same.

Jan 1, 1992

By Y. Maeda

Non-ferrous smelting furnaces generally lnstal1 a gas cooling system for treatment of waste gas containing S02. From the point of view of corrosion resistance and recovery of waste heat, the high pressure boiler system Is the best way to cool gas, however this system requires high Initial investment and relatively higher operating costs. Because the feasibility of this boiler system greatly depends on the smelting process and scale, other lower temperature systems, e.g. water-cooled Jacket system, are more suitable If the smelting process does not produce enough steam nor generate enough electricity to compensate operating cost. In addition, the water-cooled Jacket system Is simple in structure and easy to operate. For those reasons, it is applied widely. A new smelting furnace. was planned tin our factory and It was necessary to install waste gas cooling equipment. In our case, a water-cooled Jacket system was mo11e feasible because of the low gas volume and high dust content. H was also expected to operate without maintenance for ten years. On the other hand, some leakage problems with the water-cool1ed Jacket had been experienced In the past. That is because S02 in the waste gas changed into sulfuric acid which corroded the Jacket material, As the first step, several data from actual usage were reviewed to throw light on the corrosion process, and an appropriate procedure to determine the operating temperature of cooling water was obtained. For the basis of this study, a water-cooled Jacket system was newly designed and tested for three months in a pilot plant. After this system&apos;s performance was confirmed, It was installed In a new furnace as a commercial pl.ant. After one year of operation, the initial thickness of carbon steel Jacket remains almost the same.

Jan 1, 1992

By A. Pagliero

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

Jan 1, 1999