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By Li Yuhai

Kinetics of non-isothermal precipitate process and crystal growth of perovskite (CaO ? Ti02) phase in CaO-TiOz-Si02-AlP3-MgO system were studied. The experimental results show that the relative volume fraction can be described by the equation given by K. Matusita et at. and the experiential expression of average crystal radius was obtained. The particle coarsening in non-isothermal process has important effects on the crystal growth of perovskite phase.

Jan 1, 2000

By Xi-Shan Li, Qian Li, Yong-bin Yang, Li-na Cui, Tao Jiang, Jie Ge

"With regard to control environment pollution in the roasting pretreatment of sulfur & arsenic-bearing gold concentrate, roasting of double-layered pellet was proposed. In the paper, the characteristics of double-layered pellet roasting were studied. Removal and solidification rates of sulfur and arsenic were investigated as primary factors. The result indicated that the removal and solidification rates of arsenic reached up to 95.91 % and 98.95% while the sulfur was 97.19% and 97.90% respectively on the premise of adopting slaked lime as solidified agent at temperature of 6000, the package proportion of 2.14 and roasting time of 3h. However, pyrite and arsenopyrite were transformed to hematite and magnetite and product of solidification mainly consisted of calcium sulfate, calcium arsenate and calcium sulfite within optimum roasting parameters.IntroductionUtilization of refractory gold resources has been gradually concentrated on with the depletion of the gold resources which are easy to deal with in the world [1]. Sulfur and arsenic-bearing gold ore is a typical refractory gold one, in which ultrafme gold is encapsulated in the structure of metal sulfide minerals [2,3], so it gives poor recovery through direct cyanide leaching. These refractory ores need pretreatment before the process of cyanide leaching to undermine lattice structure of pyrite and arsenopyrite containing gold [4] so that the gold could touch with cyanide solution [5]. Among various methods of pretreatment, conventional roasting method is most effective, but this process generates gases such as S02 and As203 harmful to environment. Therefore solidification roasting was proposed to solve this problem occurring in the conventional roasting at the end of last century."

Jan 1, 2013

By Biao Zhou, Qian Li, Kuo-Chih Chou, Yi-Long Liang, Jie-Yu Zhang, Qun Luo

"In this work, the phase transformational behaviors and microstructural characteristics of 60Si2CrVAT spring steel were systematically investigated as a function of applied cooling rates in the range of 0.l-10°C/s. A quenching deformation dilatometer was used to austenize and quench. The dilatometric curves between length changes and temperature of samples suggest three characteristic stages could be identified as different ranges of cooling rates, which meets well with metallographic examination and the measured hardness results. As the cooling rate increases, the structure transformed from pearlite, granular bainite to finally martensite. The F + P and B zones are completely overlapping in continuous cooling transformation (CCI) curve, which indicates that this steel is difficult to become single bainite and shows good hardenability.IntroductionThe 60Si2CrVAT, a high-carbon low ally super-high strength steel developed from the ?OCT 60C2XFA and 60Si2MnA, is often used for coil spring of heavy vehicles and high-speed railway by hot deformation or cold deformation [1-3]. The addition of Si improves relaxation resistance significantly, through the refinement of tempered carbides as the result of the retardation of E -carbide conversion to cementite during tempering. Due to its deleterious effects on decarburization and toughness, the maxinJum content of Si has limited to 1.5 or 2.0% [4-5]. Additionally, V and Cr can improve sag resistance due to the precipitation of fine carbonitrides during hot rolling [6-7]. To best of our knowledge, the strengthening by precipitation of alloy carbides of Cr and V often referred to secondary hardening [8]."

Jan 1, 2013

By M. Sripathy, K. V. Sharmal

"The conventional fiber reinforced plastic does not participate in the plastic deformation or enter the large plastic deformation state during collision. On the other hand, sandwich structure allows more plastic deformation, which improves the energy absorption efficiency. The objective of this study is focused on the investigation of the crushing of sandwich structure made from sisal / coir / bamboo/ glass fabrics as reinforcement and with polyester resin to form the composites skin and with polyurethane foam as the core. Experiments were conducted, showing that the underlying crushing mechanism of sandwich structures is very different from that of solid-section thin-walled structures. When a sandwich is subjected to crushing, the core deforms in the shear mode and the face bends independently. The damage is through the width zone of crushed foam core accompanied by a residual crushing in the foam. It is shown that such damage causes a significant reduction of compressive strength. Results show that glass/polyester and bamboo/polyester skin based sandwich structures have superior compressive strength. Coir /polyester based sandwich structure come next to glass/polyester sandwich structures in this aspect which is then followed by Sisal /polyester based sandwich structures.IntroductionCellular polymeric foam sandwich structures are often employed in shock mitigating applications. The cellular polymeric foam has several favorable properties, such as, low density, relatively high strength-to weight ratio and a significant degree of crushability. This high crushability is the result of the large void ratio in such materials, which also facilitates the collapse of cell walls via bending and buckling [1]. A few feasibility studies on FRP sandwich panels show that the panels efficiently provided high mechanical performance for minimum weight [2]."

Jan 1, 2012

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

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

Jan 1, 2012

By T. A. Edison

A distinct hydrocarbon maturation anomaly coincides with the Gold Acres open pit, Nevada (Figure 1). Both atomic hydrogen to carbon (H-C) ratios and reflectance measurements of contained organic matter indicate significantly higher maturity in samples collected within the confines of the open pit than in samples from the surrounding region (not shown in Figure 1).

Jan 1, 1987

By Sung Jin Han

Magnesia-based refractory is generally used in an electric arc furnace (EAF) due to its relatively high corrosion resistance and strength at high temperatures. However, the magnesia refractory is attacked by EAF slag and thus the lining life continuously decreases. Thus, it is significant to identify the interfacial reaction between magnesia refractory and FeO-rich EAF slags. In the present study, the influence of FeO-rich slag on the corrosion behavior of MgO refractory was evaluated. The (Fe,Mg)Oss layer was observed at the slag-refractory interface and its thickness increased with increasing content of FeO in the slag. The specific reaction phenomena and formation behavior of (Fe,Mg)Oss layer were evaluated by thermochemical computing program, FactsageTM7.0.

By Xiangru Chen, Qijie Zhai, Haicheng Li, Chao Yang, Zhang Wei

The Nb-rich phase generated by the addition of trace amounts of Nb(<0.1wt%) \ and the effects of different content of Nb on the morphology and distribution of graphite in ductile iron were studied in this paper. The results showed that when the content of niobium less than 0.1wt%, the two-dimensional morphology of Nb-rich phase existed in microalloyed ductile iron were mainly regular pattern such as square, triangle, polygon etc. Besides, Nb-rich phase in large size distributed in the matrix with a certain distance from graphite. With the increasing amount of niobium, the dispersion degree of graphite diameter, average diameter and roundness increased slightly, and the number of graphite decreased slightly.

Jan 1, 2015

By Jin-yan TIE, Ke-xin JIAO, Qian Li, Hai-bin ZUO, Jian-Liang Zhang, Meng SHEN

This paper designs three factors such as temperature, pH, conductivity and three levels of orthogonal test. Temperature is a significant factor. However PH and conductivity are not significant through poor analysis. Further research is conducted on the temperature. Temperature stability is 50 . Suitable water velocity is 2.3m/s, which is calculated based on the largest part of the heat flux intensity and the corresponding water temperature should be controlled with 1.5. Meanwhile, water velocity increased has little effect on the heat transfer capabilities.

Jan 1, 2015

By Justin Karl, Ali Gordon, James DeMarco, Yongho Sohn

"Aluminum metal-matrix composites are lightweight materials that have the potential to supplant steel in many applications. The current work helps to identify the parameters that confer maximal strength and ductility. Torsion tests were performed on the as-cast aluminum metal-matrix composite A359-SiCp-30% at a variety of temperatures and twist rates. Dependence of material properties on temperature and strain rate were identified from equivalent stress-strain curves constructed from the reduced data. Examination of the microstructure was performed on the as-cast material and on fracture surfaces. A temperature-and strain rate-dependent constitutive model was applied to simulation of the mechanical response of the torsion specimen. Trends in material properties corroborate and extend trends identified previously under tensile loading with regard to temperature and strain rate dependence. Shear properties of simulated specimens agree with properties obtained through experimentation.IntroductionAluminum metal-matrix composites (A1-MMCs) have become increasingly popu1ar in recent years. While unreinforced aluminum alloys have low densities and high ductilities, they are not suitable for many applications due to their lack of strength and stiffness. To provide added strength and stiffness while maintaining favorable densities, it has become common to reinforce aluminum alloys with silicon carbide in various forms, although usually the inclusions are in the form of whiskers or particles. The result is a composite material with superior specific strength and stiffness. While whisker-reinforced composites are expensive due to the necessity of processing by nonstandard techniques and have low transverse properties when rolled, particle reinforced Al-MMCs have transverse material property values almost as high as the longitudinal properties and are not as expensive to process as whisker-reinforced Al-MMCs [1]."

Jan 1, 2012

By Donghai Li, Cheng Pan, Xuyang Liu, Xuewei Lv, Chenguang Bai

"Fine chromite ore is the common raw material to produce ferrochrome alloy through the submerged electric furnace process. The electric resistivity of fine chromite ore plays an important role in the operation efficiency because it determines the current distribution. The effect of particle size and the contact area of the particles on electric resistivity for several of chromite were investigated at room temperature, and the relationship between the electric resistivity of mixed particles and the volume fraction of lump ore to fine ore was also studied. The results shown that the electric resistivity increases with the increase of particle size, and the electric resistivity of mixture decreases with the increase of volume ratio of fine ore.IntroductionChromium is one of the most important alloying elements in manufacturing of stainless steel that used at high temperature and corrosive environment applications [I, 2]. As the raw materials to be charged into the steel, ferrochromium alloys and charge chromium are produced directly by smelting of chromite ore with the reducing agent in submerged electric arc furnace (SAF). During the process, the oxides of chromium and iron were reduced by carbon and meanwhile the electrical energy were consumed [3,4]. The ideal industrial process is to achieve high recovery level of Cr and Fe with minimal power consumption. In SAF process, the electric resistivity of charge stock has significant effect on the current distribution, which determines the heat distribution, molten bath structure and chemical reactions in the furnace. High resistance of the charge is desired to reduce the current distribution through the charge stock, thus the electrodes may insert into the charge stock with proper depth to form a high temperature arc heat source, and proper smelting can be realized[5]."

Jan 1, 2012

By Samir N. Shoukry, Mourad Y. Riad, Gergis W. William

"Setting of concrete material is defined as the transitional period between states of true fluidity and true rigidity. Initial and final setting times are measured in the laboratory on the mortar sieved from the mix in a controlled environment where temperature and moisture values are constant. On the other hand, field applications are held in outdoor environments where environmental variations have direct impact on setting time values. In this study, initial setting time of class K concrete, usually used for bridge decks and concrete pavements, are investigated highlighting discrepancies between laboratory and field measurements. 72 mixes have been cast in variable environments and collected data from concrete mixes and the ambient conditions are reported. In light of the collected data, the effects of variable setting times on early age cracking of concrete material are studied and means to minimize such cracks are presented.BackgroundSetting of concrete material is defined as the transitional period between states of true fluidity and true rigidity [1]. Continuous hydration of the cement within the matrix transfers the mix from a state of setting to hardening. Initial and final Setting times are measured in a laboratory setting following ASTM C 403 specifications. Initial setting approximates the time at which the cement paste can no longer be plastic under compaction (or can be handled in a proper fashion), while the final setting approximates the time at which hardening occurs. The standard test described in ASTM C 403 is conducted on the mortar sieved from the mix (paste passing from 4.75 mm sieve opening). Initial and final settings are described as the elapsed time after the initial contact of water and cement till the mortar reaches a penetration resistances of 3.5 MPa (500 psi), and 27.6 MPa (4000 psi) respectively."

Jan 1, 2012

By Jing Zhan, Chuanfu Zhang, Yonglin Yao

"The Ni/Co arbitrary ratios of fibrous precursor were investigated during coordinated coprecipitation by changing the precipitating medium. The results show that the original molar ratio ofNi2+ to Co2+ in reaction solution can be maintained in the coprecipitate at pH'.'05.0 and the coprecipitate is single phase solid solution using water and water-X precipitating medium. But the original Ni/Co ratios are no longer kept and composition of the coprecipitate is not uniform at pH>5.0 in water precipitation medium. In order to obtain the precursors with the required morphology and accuracy Ni/Co ratios, the optimum conditions of fibrous precursors were chosen as follows: ammonia used as complex agent and pH adjustor, water-X solvent as precipiting medium, oxalate as coprecipitated agent, 8.0-8.4 for pH value, 50-70°C of reaction temperature, 0.5-0.8 mol/L of initial nickel and cobalt salt concentrations and excesses of oxalic acid of 10% - 20%.IntroductionNi-Co alloy as an important transition metal alloy with high mechanical strength, good anti-deformation, corrosion resistance, thermal conductivity, thermal stability, electrical conductivity, electrical contact, and special magnetic properties indicates that it can be used as high-temperature catalyst, special magnetic material, high-temperature electrochemical devices, and so on [1-6]. An ideal composite powder should have an appropriate stoichiometric ratio, good uniformity of chemical composition, appropriate phase, low impurity content and small particle size [7]. Similarly, the composition of nickel-cobalt alloy powder has an important impact on its crystal structure, properties and applications. Guo[8] found that magnetisms of CoxNi1-x such as magnetic anisotropy, curie temperature, and the shifts of the spin steering are very sensitive to the composition of alloy powder."

Jan 1, 2013

By Xinghua He, Shujing Zhu

"In this paper, the chemical composition, the content and the leachability of heavy metals in dredged sludge are tested and analyzed. It is shown that the leachability of Pb and Cr exceeds the leaching toxicity standard, and so the dredged sludge is considered as hazardous waste and must be solidified. The effect of solidifying the dredged sludge by the hydraulic ash-slag cementitious composites is studied, and it indicates that the heavy metals can be well immobilized if the mass fraction of the dredged sludge is appropriate. The heavy metals are immobilized within the hydraulic ash-slag cementitious composites hydration products through either physical fixation, substitution, deposition or adsorption mechanisms.IntroductionDredged sludge is classified as a hazardous waste because it usually contains concentrated heavy metals and chlorinated organic compounds, as well as soluble salts, and is also composed of very fine particles. Moreover, inorganic pollutants are typically associated with soluble compounds, which are, therefore, highly leachable from dredged sludge when dredged sludge is contacted by a liquid medium[l1. Thus, dredged sludge must be stabilized in order to reduce its environmental impact on the final disposal site. The frequent means of dredged sludge disposal used include(!) Chemical stabilization (2) acidic extractionChemical stabilization is translating mobile heavy metals into low dissolution and low toxicity form through chemical reaction. The commonly chemical medicaments are sodium hydroxide, soldium sulfide, thiourea, EDTA. But Zhao et al [ZJ found sodium hydroxide is not fit for Pb stabilization, the other three are effective, but the chemical properties of sodium sulfide are not stable, thiourea and EDTA are very expensive, and so it is very difficult to apply them. Moreover, because of the complexity of heavy metal conformation and dredged sludge composition, it is very difficult to find a cheap and prevalent stabilization medicament in point[31 ."

Jan 1, 2013

By Thomas Brynjulfsen, Merete Tangstad

"Manganese ore fines, generated during mining and transportation, can not be added to the submerged arc furnace directly as they will prevent even gas flow through the burden. Low gas permeability in the burden will lower the degree of pre-reduction of ore and subsequently increase the carbon and energy consumption of the process. In order to utilize manganese ore fines in the furnace they are agglomerated into sinter, pellet or briquettes. The agglomeration process will however change the reduction properties of the ore. In this work the melting and reduction properties of sinter has been investigated.The melting temperature and melting mechanisms has been studied. The mineralogy of the raw ores and agglomerated has been found using XRD, and the composition established using EPMA(WDS). The effect of adding fluxes such as dolomite and quartz has also been investigated.IntroductionManganese metal is produced in a submerged electric arc furnace or in blast furnaces. The reduction of manganese oxide in blast furnace has in the recent years become more unusual due to the high consumption of reducing carbon material[5]. Manganese metal for alloying in steel usually contains silicon and iron, and are therefore called ferro manganese and silicomanganese.During mining, transportation and handling the manganese ore is broken up into different size fractions. The larger lump are used directly in the electric arc furnace, but the finer materials can not be added without treatment. The fine ore can disrupt the flow of CO and CO2 gas through the burden, subsequently reducing the degree of pre-reduction. The fine fractions must therefore be agglomerated into larger lumps, in order to promote gas flow. This can be achieved through a number of different processes. The agglomerate used in this work has been sintered, which means that is has been partly molten and reduced, in order to create bigger lumps."

Jan 1, 2012

By R. T. Jr. Faria, H. Vargas, R. Toledo, S. Cosin, V. P. Souza

"With the purpose of decrease environmental impact, caused by industrial residues (just discarded in the environment) and clay extraction in the ceramic industry, sanitary ware wastes were incorporated into clay. In contrast, it is important to evaluate not only the technological essays but also gases emissions in the ceramic firing process. The pollutant gases emitted in ceramic with residues can be in much larger concentrations than that in a pure clay ceramic firing or, on the other hand, can decrease the pollutant gas concentrations. With the aid of thermal analyses and photo acoustical techniques it was observed that sanitary ware waste can reduce the C02 emission. The gas emissions were shown as in function of firing temperature from 300 DC to 1100 DC. In order to analyze phase transformations during the firing process, clay samples and wastes were both analyzed by x-rays fluorescent chemical analysis and x-rays diffraction.IntroductionResearch works on the structural and physical changes that wastes, mainly industrially produced, cause to the final ceramic product has been rapidly expanding in these last two decades. See, for instance references in [1]. In spite of these examples of a continuous effort to incorporate wastes into clay ceramic motivated by technical and economical advantages, environmental issues are still a matter of concern. However, the gas emission due to the clay firing process and its related atmospheric pollution may be enhanced as a consequence of an incorporated waste [2]. It is known that the firing of clay ceramics in conventional furnaces using fuels such as wood, charcoal, heavy oil and natural gas generates appreciable amounts of gaseous components, mainly carbon dioxide (CO2), carbon monoxide (CO) and methane (CH4). Additionally to the atmospheric pollution, these gas sets could be harmful to the human health and can corrode equipments [3,4]."

Jan 1, 2012

By N. R. Green, N. J. Humphreys, D. McBride, T. N. Croft, M. Cross, D. M. Shevchenko

"Centrifugal casting offers a route to high quality products in difficult to cast high temperature low superheat alloys and thin section molds. Under centrifugal forces metal is forced into thin sections and can fill thicknesses of less than a millimeter. However, due to the high liquid metal velocities there is a high risk of surface turbulent flow and air entrainment within the liquid metal. The combination of interacting flow-thermal-solidification phenomena and associated defects is a challenging modeling task which the authors have previously described and validated. Capturing the metal-air interface, on what are inevitably complex three dimensional geometries, results in highly computationally expensive simulations and simulating a single cast can take weeks on a single processor. This contribution reports on modeling a complex centrifugal cast, gas entrainment, bubble transport and solidification, employing meshes of up to a million elements and investigates the scalability of the model on high performance clusters.Introduction The ultimate goal of any casting procedure is to produce a defect-free product. For difficult to cast alloys, such as Titanium, centrifugal casting has a number of advantage over conventional gravity methods [1]. In the casting of thin sections, such as turbine blades, the metal is forced into the thin sections under centrifugal forces. The centrifugal force can overcome the backpressure due to surface tension and the metal can fill mould sections with thicknesses substantially less than a millimeter. However, the materials used in these castings [2] tend to be highly reactive and requires low superheat. High liquid metal velocity gives rise to a high risk of free surface turbulent flow and of associated entrainment through free surface turbulence [3] and trapping of gas present in the flow [1]."

Jan 1, 2012

By Roger Wilmoth

Exposed, open pit mine highwalls contribute significantly to the production of acid mine drainage (AMD) thus causing environmental concerns upon closure of an operating mine. Four innovative technologies were evaluated under the U.S. Environmental Protection Agency?s, Mine Waste Technology (MWTP), Prevention of AMD Generation from Open-Pit Highwalls Demonstration Project. This project is funded by the U.S. Environmental Protection Agency (EPA) and jointly administered by the EPA and the U.S. Department of Energy (DOE) through an Interagency Agreement. The objective of the field demonstration was to evaluate the technologies ability to decrease or eliminate acid generation from treated areas of the highwall in comparison an untreated highwall area. The field demonstration was performed at the Golden Sunlight Mine (GSM) a subsidiary of Placer Dome U.S., located near Whitehall, Montana. GSM is an operating gold mine. The highwall at GSM was divided into five plots measuring 15.24 by 15.24 metres (m) and each technology was assigned a plot with the fifth plot being used for comparison as a background control plot. The four technologies were spray-applied. The applied insitu treatment technologies included: 1) A modified, furfuryl alcohol resin sealant, utilizing wood and agricultural by-products to coat the rock surface. 2) EcobondTMARD, a phosphate based process that forms a stable, insoluble compound, coating the rock surface. 3) Two ARD passivation technologies, magnesium oxide and the Dupont technology developed to create an inert layer/coating on the pyrite, preventing oxidation. The technologies were evaluated using the following methods: 1) ASTM D 5744-96, Accelerated Weathering of Solid Materials using a Modified Humidity Cells, 2) mine wall residual wall rinse sampling, 3) microscopy, and 4) core drilling followed by water injection testing.

Jan 1, 2003

By M. Rockandel

"Universal Dynamics Ltd. of Vancouver, Canada has developed, patented and commercialized the ""REMERC"" process for the treatment of mercury contaminated sludges and soils. Mercury is extracted into an acidified and oxidizing, sodium chloride brine solution. REMERC was initially developed to treat mercury contaminated EPA listed wastes (K106) generated by the chlor-alkali industry. More recent work has expanded the capability;' of REMERC to include remediation of mercury contaminated sites, equipment and building materials.In the process mercury is currently recovered from solution by cementation on iron powder in an agitated reactor. The process recovers high purity elemental mercury (99.9% purity). Cementation typically recovers about 90-95% of the mercury in 30 minutes. Higher recovery is not necessary because of the recirculation of the leach solution. When treating highly contaminated chloralkali wastes (5-13% mercury content), REMERC will reduce the mercury laden solutions from 400-1,000 mg/L mercury to 50-100 mg/L. In the treatment of less concentrated wastes «1,000 mg/kg mercury) such as those encountered in site remediation, the treated solutions will generally contain 10-20 mg/L mercury. Cementation while being simple and able to achieve the required recovery has the. undesirable properties of; requiring a solid-liquid separation and adding iron to solution which must be precipitated, ultimately increasing the weight of residue to landfill. .The potential advantages of electrolysis were recognized early in the development of REMERC. Mercury electrolysis is well known in gold and chloralkali processing. Initial testwork utilized a liquid mercury cathode and a coated titanium anode both common to chloralkali producers. The mercury cathode appeared susceptible to polarization and solution impurities significantly affected performance. Agitation of the mercury pool improved performance but it was still not possible to achieve the reduction objectives. Current efficiencies were low, near 10%, and it was apparent that a relatively large cathode pool would be required to limit the current density. A number of electrode combinations with and without a membrane were then tested in a vertical electrode' configuration but the desired performance was not obtained."

Jan 1, 1997

By Akram Alfantzai, Farzad Mohammadi, Maysam Mohammadi

"Degradation of lead anodes has always been a major concern among the electrowinning industries. In this study, the effect of agitation of the zinc electrowinning solution on the integrity of lead anodes was investigated. Galvanostatic experiments were performed at 37±0.5°C using 0,600 and l000rpm magnetic stirring rates for 24 hours. The Pb02 layer formed on the anode surface was reduced to PbS04 (discharged). The discharge information was used to calculate the amount of Pb02 present on the surface. Weight loss measurements along with the discharge calculations revealed that the degradation rate of the lead anode increased as the solution was stirred more vigorously. Furthermore, the amount of remaining Pb02 on the surfaces was decreased as a function of solution velocity. Therefore, it may be concluded that, degradation rate oflead anodes is controlled by detachment of the corrosion products from the surface rather than by electrochemical reactions. IntroductionElectrowinning is one of the extraction stages of zinc, in which pure zinc is deposited from acidic solution after froth flotation, roasting and leaching processes. The anode electrode materials play important roles in the electrowinning process. Their electrocatalytical capacities determine the oxygen evolution overpotential, and consequently the cell potential and energy efficiency of the zinc electrodeposition [l]. Purity of the zinc deposited on the cathode is affected by the solubility and corrosion resistance of the anode materials. Using insoluble materials as anode in the electrowinning leads to the higher purity of the deposited metal on the cathode[2]. Lead (Pb) and its alloys have been used as the anode in the zinc electrowinning because of its special properties such as relatively low cost, low melting point, insolubility in solutions containing sulphuric acid and high conductivity in both states of metallic and oxidized [3, 4]. In zinc electrowinnig, zinc reduction occurs on the cathode (reaction 1) and the oxygen evolution reaction (OER) (reaction 2) is the main anodic reaction [5, 6]."

Jan 1, 2013