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By M. S. Moats

A considerable amount of research has been conducted to determine the causes of anode passivation. Chemical and electrochemical reactions that occur after passivation have received little attention. Chronopotentiometry, linear sweep voltammetry, cyclic voltammetry, and impedance spectroscopy have been used to elucidate three reactions that occur after passivation of commercial copper anodes. These involve the dissolution of silver and subsequent cementation and transformation of selenides, the oxidation of lead sulfate to lead oxide, and oxygen evolution. The amount of silver dissolution depends on the silver content of the anode, the time to passivation, and the molar ratio of Ag/(Se+Te). The oxidation of lead from PbSO4 to PbOx explains a potential plateau of oxygen evolution. Silver affects the duration of oxygen evolution on the PbOx. Anodes containing kupferglimmer display a characteristic oxygen evolution potential. It is believed that kupferglimmer provides a lower overpotential for oxygen evolution than the other slime phases or passivated surface.

Jan 1, 1999

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 Michael Meyer

In the past shredder fluff was discarded in landfills, but shrinking landfill space and the partly hazardous content of the fluff as well as its caloric value, all resulted in efforts to turn this waste problem into a an energy resource. In order to produce a fuel, the inorganic compounds have to be removed. Extensive analyses and particle size measurements were made on fluff from various shredder. For optimal separation all particles are reduced to a uniform, relatively small size. In a subsequent combined - screening and air classification - process, successful separation into organic and inorganic fractions is achieved. The inorganic fraction is treated in a heavy media or an eddy-current separator to recover the valuable metals, while the organic fraction is now suitable for thermal processing, such as fluidized bed gasification and using the resulting carbon as a chemical reagent.

Jan 1, 1995

By D. I. Chalmers

The Brockman rare-metals and rare earth resource is located within volcanic and volcanogenic sediments of the later Proterozoic Halls Creek Group in the East Kimberley region of Western Australia. Exploration including surface trenching, percussion and diamond drilling has defined a major resource of rare-metals and heavy rare earth elements. The host&apos; is a steeply dipping ash-flow tuff, described informally as the Niobium Tuff, enriched in zirconium, hafnium, yttrium, niobium, tantalum, rare earth elements, gallium and beryllium. The mineralization is fine- grained (<20 micrometres) and is the result of alteration and re- mobilization of comparatively simple precursor minerals such as columbite and zircon by fluorine-rich deuteric solutions that were retained in the tuff following eruption. The ultra fine-grained structure of the tuff precludes mineral liberation and separation by physical methods. However, values can be converted to water soluble sulphates by reacting with concentrated sulphuric acid at 250°C. The solution containing aluminium, niobium, tantalum, zirconium, hafnium, yttrium, rare earths and gallium can then be processed to pure products in a sequence of solvent extraction and ion-exchange steps. As a result of these processing techniques, the commercial products obtainable from the resource include mixed rare earth and yttrium concentrates, zirconium-hafnium concentrate, niobium-tantalum concentrate and ceramic grade alumina. Further separation could result in high purity products suitable for ceramic and electronic applications.

Jan 1, 1992

By H. Fukushima, T. Ohgai, N. Baba

The electrodeposition behavior of Zn and the morphology of the deposited Zn were studied in electrowinning solutions containing polymer additives such as gelatin and polyethylene glycol (PEG). The cathode potential was shifted in a less noble direction and the polarization resistance for Zn deposition increased with increasing concentrations and molecular weights of both gelatin and PEG added to the electrolytic solutions. However, when the molecular weights of these additives exceeded about lxlO4, the cathode was depolarized and the polarization resistance for Zn deposition decreased with increasing molecular weight. The crystal grain size and the (002) orientation of the deposited Zn became smaller when the concentration and molecular weight of the additives increased, and the cathode was polarized.

Jan 1, 2000

By Michael S. Moats, Daniel Kim, Shijie Wang

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

Jan 1, 2012

By Daniel Kim, Michael Free, Justin McAllister, Urian Marshall, Shijie Wang

"Cathode impurity levels of electrorefined copper were evaluated based on 1/10* scale laboratory electrorefining tests. Cathodes were evaluated near the top, mid-section, and bottom sections of cathodes on both the set and mold sides and strip and scrap cycles. Slime weights were measured, and slime and electrolyte samples were also evaluated for impurities. Results from these tests have been compiled and compared to evaluate the effects of changes in operating conditions and electrode location on cathode impurities.IntroductionMany types of impurities are commonly found in commercial copper electrorefining anodes. The smelter operations that produce the anodes process concentrates that contain a wide variety of impurities that vary based on the mineralogy of the ore. Most anode impurities are removed during electrorefining. However, a portion of the anode impurities is incorporated into the copper cathode product. The mechanisms by which impurities are transported from the anode to the cathode are not well understood. Some impurities can be transported as anode slime particles to the cathode where they are incorporated into the cathode. Other impurities can be transported as dissolved species that are electrochemically reduced with the copper to become part of the cathode. Although research has been performed on anode slimes and impurities [1-4], there is a need for additional information regarding the relationships associated with electrorefining cycles, electrode faces, local electrode positions, anode impurities and specific cathode impurities. The objective of this study was to evaluate lead, arsenic, and antimony cathode impurity trends associated with electrorefining cycles, electrode faces, local electrode positions, and anode impurities. A variety of techniques including electrolyte filtering, anode heat treatment, high electrolyte arsenic concentration, high arsenic and/or lead in anodes, flocculation of slime particles, and appropriate current density control were used to vary cathode impurity levels. Each test was performed only once for a strip cycle and once for a scrap cycle. Consequently, the results for the individual conditions are preliminary and are not the focus of this study. However, the collective set of data with varying impurity modifying techniques provides a broad range of impurity levels, and the associated trends with respect to lead, arsenic, and antimony are discussed in this paper. Approximately 180 analyses of copper cathode were used to track the antimony, arsenic, and lead impurities. Eighteen anode slime samples were also analyzed for antimony, arsenic, and lead."

Jan 1, 2012

By D. J. Brennan

A techno-economic study is in progress, examining process and product options for treating smelter gases containing various concentrations of sulphur dioxide. Key contenders have been examined within an Australian context using the following criteria: * Markets for products * Capital Costs * Operating Costs * Waste streams generated Product options considered thus far are sulphuric acid, sulphur, calcium sulphite and gypsum. The development of an appropriate overall framework for evaluating process and product options is discussed and findings thus far presented. The emerging techno-economic study offers promise as a constructive guide to future policy decisions by industry and government.

Jan 1, 1994

By Weyman Dunaway

This paper will present a description of the development and commissioning of the world?s most efficient process for manufacturing high purity aqueous zinc bromide. The method for making aqueous zinc bromide from metallic zinc and bromine comprises contacting zinc with bromine dissolved in a reaction solvent containing a metal halide salt. The reaction temperature is maintained at less than 60°C. The reaction solvent preferably comprises an alkali, alkaline earth, or transition metal halide; the halide salt preferably comprises a chloride or a bromide. One preferred method includes the step of recirculating the zinc bromide product stream back to the reaction vessel. The reaction vessel can be either a one stage or a multiple stage reactor. The resulting product stream is a high density aqueous zinc bromide solution. The process is so novel that Tetra Technologies, Inc. was awarded US Patent Number 6,036,937.

Jan 1, 2006

By Pertti Pekkala

Outokumpu has 25 years of experience in the SX area. The development of the solvent extraction plants responds to an ever increasing demand for lower operational costs wd for adaptability to process disturbances with minimized risks. In this paper the features of the VSF ("Vertical Smooth Flow") SX technology are described, such as the separated pumping and mixing, the homogenous gentle mixing, the droplet coalescence and the ultra pure settling. A major advantage of the mixing technology is the high stage efficiency of above 99 per cent. The connection between this and some features of the settler front section is clarified. The present design of VSF plants is based on experience of existing operations at, for example, Zaldivar, Radomiro, Morenci, Kokkola and Harjavalta. These production plants cover a unit capacity range of 60 to 3,600 m3/h expressed as a total flow. It is evident that there are no restrictive factors to increase the total flow up to 5,000-6,000 m3/h by introducing the VSF technology. The copper SX technology has a long history reflecting many individual features of the separate copper SX plants. Still it is necessary to verify all actual running parameters by pilot tests taking into account impurities, chemicals used etc. The design of SX plants is not only about the delivery of equipment but also a process concept, and it is best tailor-made and adapted to specific local requirements.

Jan 1, 1999

By A. L. Davies

The MTDATA computer software package consists of a rigorous implementation of an algorithm for calculating chemical phase equilibria by the technique of Gibbs free energy minimization and a database of the thermochemical properties of common materials, such as slags, mattes, metals, gases and aqueous solutions. We have used MTDATA to contribute to our understanding of the chemical reactions occurring in several specific unit operations of the Kennecott Utah Copper Garfield Smelter. The following two examples illustrate the range of environments to which the method is applicable. Calculation of the liquidus phase relations of the FSF fayalite and FCF calcium ferrite slags helped in the early diagnosis of several operating problems. Calculation of the deportment of fluorine between the FSF offgas and the FSG scrubber liquor helped in the identification of operating conditions under which significant hydrogen fluoride concentrations could be introduced to the contact section of the acid plant. Without the painstaking assessment of solution phase properties undertaken over many years, these calculations would not be possible.

Jan 1, 1999

By D. W. Collins

Several organic and inorganic substances are widely used to control deposit structure and morphology during the electroprocessing of copper. Methods for monitoring the levels of thiourea, glue and guar gum during electrorefining and electrowinning have been successfully developed under the trade names of Reatrol and CollaMat. Other instrumental methods have been developed for additives and decomposition products associated with the electroplating of copper and other metals. Generally, these methods have been found to be either insufficiently sensitive or lacking in the desired selectivity for some or all of the additives. These procedures have mostly employed DC techniques; i.e., cyclic voltammetry, Tafel analysis, etc. In this work, chronopotentiometry (CP) and AC voltammetry were used to examine the interaction of glue, guar gum, thiourea and chloride during the electroplating of copper onto a platinum electrode. In addition, the interactions between the additives have been explored. It was found that glue in pure electrolyte (H2S04 and CuS04 only) had no effect on the chronopotentiogram. Glue was only active if chloride ions were present. The addition of thiourea resulted in several different chronopotentiograms depending on the presence of either chloride or chloride and glue. Thiourea used in conjunction with glue and chloride showed a significant increase in the polarization during copper deposition when compared to the electrolyte containing only glue and chloride. The use of a modified channel electrode further increased the sensitivity of CP. The use of AC voltammetry was explored as a technique to monitor some of the additives. AC voltammograms have more spectral detail then their DC counterparts and it is possible to monitor some of the additives at very low concentrations with AC techniques.

Jan 1, 1999

By Gaifeng Xue, Lei Zhang, Aimin Duan, J. Y. Hwang, Lina Wang

"The removal of chemical oxygen demand (COD) from coking wastewater was experimentally investigated using a three-dimensional electrode reactor. The experimental results showed that the refractory organics in coking wastewater can be effectively removed by this process, and COD removal efficiency was affected by the operating parameters, such as electrolytic retention time, particle electrode dosage, initial pH, current density, aeration amount and electrical conductivity. The experimental results show that the three-dimensional electrode could have a COD removal efficiency of more than 60% and a running cost of no more than 6 YUAN (RMB)/t. This indicates the great potential of a three-dimensional electrode reactor in engineering applications as an advanced treatment methods for coking wastewater.IntroductionCoking wastewater is generated from coal coking, coal gas purification, and by-product recovery processes of coking; it is composed of phenolic compounds, heterocyclic compounds, polycyclic aromatic hydrocarbons, ammonia, cyanide, polycyclic nitrogen-containing aromatics, acyclic compounds, etc. Most of these constituents are refractory, poorly biodegradabile, toxic and carcinogenic [1-3]. Currently, coking wastewater is usually treated by different forms of A/O biological nitrogen removal processes as the primary treatment means, but the aforementioned processes are not efficient enough to meet the requirements of the National Discharge Standard in China (GB13456-1992). According to the continuous requirement on improving environmental protection for the coking industry (revised 2008), increasing wastewater utilization ratios and reducing the discharge of effluent in the coke industry have to be implemented for cleaner production and sustainable development. Therefore, advanced technologies need to be developed to treat coking wastewater and reutilize the product as industrial cooling water, which would be one of the best choices to achieve zero discharge of wastewater and reduce water consumption per ton of steel produced. In this study, a three-dimensional fluidized bed electrode reactor was adopted for the advanced treatment of coking wastewater, and the effects of operating conditions, including particle dosage, initial pH, current density, supporting electrolyte, as well as aeration amount on the COD removal rate, were investigated. Its running costs were also estimated."

Jan 1, 2012

By Roald Ysteboe, Finn Olesen

"Elkem has developed a process that utilizes SPL as a raw material for pig iron production. This process will be demonstrated in industrial scale during 2008 and 2009. The process developed produce iron, and the reduction material used, is the carbon present in the SPL. The iron source could be either virgin iron ore or waste/recycled material from the steel industry. The SPLrefractory and bath material is dissolved in the slag produced. The slag is designed so that any leaching of environmentally dangerous elements is minimized. This process can in addition to SPL, consume other types of waste derived from the primary production of aluminium. Elkem intends to supply this demo project with SPL and other waste products from external sources, domestic as well as international ones.IntroductionSpent Pot Lining (SPL) is generated when an electrolytic cell for producing aluminium is taken out of service and the refractory and carbon lining is removed from the steel potshell.The yearly generation of SPL world wide is exceeding 500 000 tonnes. The major amount of this quantity is stockpiled or land filled, unprocessed.SPL contain large amount of water soluble fluorides and some amount of cyanides and is classified as hazardous waste in most countries."

Jan 1, 2008

By Magdelinka Padenkova-Yaneva, Emilia Christova Kostakeva

"Environmental protection is becoming over the years an increasingly significant problem of mankind. Up to the last decade the only way to make the domestic waste harmless in Bulgaria was deposition on uncontrolled landfills without undertaking actions for protection of the soils. This also caused pollution to spread into the surface and underground waters and that is why actions are now undertaken for remediation of contaminated soils. This is achieved by developing projects for the closing down of polluted sites. In the present paper some projects for closing down of polluted areas are discussed. The actual conditions are examined and project decisions for preventing the surface waters from penetrating into the waste are presented. In this way the pollution of the soil is stopped and the soils are gradually remediate.IntroductionSoil is the topmost layer of the earth crust. It consists of mineral particles, organic substances, water, air and living organisms and is an extremely complex and changing living environment. Soil is a non-renewable natural resource which is of considerable importance in a number of crucial processes (production of foods, storing, filtrating and turnover of many substances, including water, carbon and nitrogen). It also serves as a basis for human activities, shaping the landscape, ground on which cultural heritage is built, and source of raw materials. These functions of soil must be protected both because of their social and economic significance and from the point of view of environmental protection.The processes of erosion, loss of organic substances, compaction, salination and contamination contribute to the degrading of soils accompanied by a negative impact on human health, natural ecosystems and changes in climate, as well as on the economy. All these make it necessary to protect soils from contamination. Over the last years intensive work started in Bulgaria for the construction of controlled sanitary landfills for rendering municipal solid waste harmless. Pursuant to Bulgarian legislation, in these controlled sanitary landfills measures are undertaken for protecting the soils from contamination through appropriate project decisions – the filtration of the products from the biological decomposition of waste into the adjacent sites (soils) and, therefore, the contamination of the surface and underground waters is prevented. At the same time the purity of air is maintained, human health is protected and conditions are created for including the controlled sanitary landfills into the surrounding landscape."

Jan 1, 2008

By Jouko Kallionen

Advanced Flotation Technology is the application driven design of flotation cells to achieve the optimum performance for each type and grind of flotation. This can be applied to roughers, scavengers, cleaners and specialty cells such as those to float hydrocyclone underflows in both primary and regrind circuits in order to reduce overgrinding. Standard, engineered, components are matched to provide mechanism design and cell dimensions for each case according to feed parameters and flotation type. Advances in process control have been achieved with high level controls and operator information data. This has gained a higher degree of understanding of cell operation and ore type being processed. Excellent results of this Advanced Flotation Technology in large scale porphyric copper ore have been achieved and designs through 7000 cu ft (200 m3) are currently available for high capacity concentrators. This paper will detail how flotation cells are more responsive to the exact requirements of the duty specified.

Jan 1, 1999

By Hai-Peng Guo, Lu Jiang, Xiao-Man Yan, Bing Xie, Hong-Yi Li

Traditional, calcium compounds cannot be used in vanadium extraction processing due to the limitation of sodium roasting technology, which results in unsatisfied dephosphorization for vanadium-containing hot metal in converter and thus increasing the dephosphorization burden for subsequent steelmaking. The calcium roasting technology is an alternative for vanadium extraction and allows adding lime into vanadium slag in converter. In the present study, vanadium was leached by soda from roasted vanadium slag with high calcium content. Effects of roasting temperature and time, leaching temperature, Na2CO3 concentration andliquid to solid ratio on vanadium leaching rate were studied. The results show that 94% of vanadium was extracted by roasting the vanadium slag at 950℃ for 2.5h and then leaching in 160g/L Na2CO3 liquid at 95℃ for 1h with liquid to solid ratio of 10:1 ml/g. Impurities of Si and P reacted with calcium and formed insoluble Ca2SiO4 and Ca3(PO4)2 respectively.

Jan 1, 2015

By A. Filzwieser

The highest current density suitable for the electrowinning process is between 50 to 60 % of its limiting current density. One of the most important influences on the limiting current density is the thickness of the hydrodynamic boundary layer near the electrode surface. Therefore, the fluid flow in a copper electrowinning cell is calculated. The numerical simulation - using the CFD-software package FIRE® - considers all three different types of the fluid flow, namely, the natural convection, the forced convection by electrolyte circulation and the forced convection by electrochemically induced gas stirring. The simulation of natural convection is based on the different density values in the boundary layer at the electrode surface given by a density/concentration correlation. The copper concentration - linked with the current density by Faraday law - is solved by an additional transport equation. The simulation of the forced convection by the electrochemically-induced gas stirring is done by using a real two-phase calculation. That means that all differential equations are solved again for the second phase. The numerical solution of the fluid flow field is compared with the results of LDA- measurements, which were done in a special cell. The software for the LDA enabled a calculation of the void fraction possible and therefore a rough estimate of the mass transfer coefficient through the prevailing gas bubble induced convection can be made by assuming the influence of relative bubble volume.

Jan 1, 1999

By Adam J. Gesing

The eddy current separator (ECS) is designed to separate nonmagnetic (nonferrous) electrically conducting (metallic) particles from nonconductive residue. Nonferrous metallic particles are repelled out of the material stream passing over the eddy current rotor (ECR). The rotor is housed in a fiberglass composite outer shell that serves as a conveyor head pulley. This results in the desired metaVnonmeta1 separation. The behavior of ferromagnetic particles, mainly iron and iron oxide (i.e. rust), is quite different. These particles are strongly attracted to the magnets and the smaller particles tend to align their long axis in the direction of the magnetic flux. Since the direction of the flux changes with the passage of each magnet pole, the small particles spin at very high rates causing wear of the belt and of the composite outer shell housing the ECR. Large particles, when trapped under the ECS belt, cannot spin, but can be heated by the eddy current effects and subsequently can burn through the composite outer shell. We discuss the practical implication of this behavior of iron and rust on the design, performance and maintenance of eddy current separators.

Jan 1, 1999

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