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By Ho-Sang Sohn

Copper concentrate particles of 200 to 300 mesh size were fed from the top of vertical reaction tube of 2.8 cm ID and 2 m long with an O2-N2 gas mixture. The reaction tube was heated to 900 K to 1100 K. The residence time of the particles in the reaction tube was about 1 second. The copper concentrate particles were very rapidly oxidized and melted down during their descent in the reaction tube. The particle temperature were calculated by combining an un-reacted core model, mass transfer between gas and particles, and heat transfer between gas, particles and tube wall. The particle temperature reached its maximum within a distance of 60 cm from the top of reaction tube, and it attained at 2000 K at higher oxygen partial pressure. The most particles were melted at the oxygen partial pressure above 20 kPa. An appreciable amount of As, Sb and Pb in the concentrate particles was eliminated in the upper portion of the reaction tube and the rate of elimination are explained by the rate of mass transfer of volatilized species through the gas film on the particle surface and the variation of particle temperature during the descent.

Jan 1, 2006

By Vânia L. L. Andrade

Igarapé Bahia Mine is located in Carajás area, northern Brazil. Currently Companhia Vale do Rio Doce operates there a CIP / heap leaching plant treating an oxide gold ore containing about 4 g Au /t and 0,2% Cu, which produces 11 t of gold per year. Recent geological survey has identified a signifcant copper-gold reserve underneath the oxide gold ore. The processing aspects of this copper-gold sulphide ore are described in this paper. It includes ore characterization studies, grinding and flotation tests, orebody variability assessment, flowsheet selection and preliminary economical evaluation Emphasis is given to studies aimed at depressing fluorine bearing minerals to achieve a clean and marketable flotation concentrate.

Jan 1, 1999

By Jin Liu

The mechanism and rate of carbon reduction of each of the phases that are formed in the flash flame, i.e. sulfide (matte) and oxysulfide, was investigated. Graphite-slag reduction was conducted for comparison purposes. The objective of these tests was to measure the rate of solid graphite reduction of respectively matte, oxysulfide, slag, and matte+slag mixture at different temperatures. More in particular, these tests were expected to permit understanding and explaining the reduction mechanism of each material by comparing the respective reaction rates, product reaction gas compositions and CO/CO2 ratios, reduced material assays, activation energies, and other relevant parameters. Direct visual inspection of the test crucibles would provide additional information.

Jan 1, 2006

By M. A. Gerdel

In carboxylate collector flotation of bastnasite from other semisoluble salt type minerals such as barite various modifiers must be added in order to achieve selective flotation. One such modifier is a lignin sulfonate. It may function in part by acting as a sequestrant for metal ions present, preventing autoactivation in the system by metal ions derived from the minerals themselves. It also functions as a depressant for both bastnasite and barite, chemisorbing on both. However, it is shown that the lignin sulfonate functions as a much stronger depressant for barite than for bastnasite. It is suggested that the; strong depressing action on barite is related to a good fit of the sulfonate into the barite structure.

Jan 1, 1989

By Henry Freiser

For the last several years, a systematic investigation of the equilibrium extraction behavior of selective tervalent lanthanides with representative chelating extractions of a variety of chelating agent families has been undertaken for the purpose of learning how to obtain chelating extractants of improved selectivity for separating individual lanthanide ions. The equilibrium extraction data (expressed as log Kex) for each reagent system are linearly related to the reciprocal ionic radius of the tervalent lanthanide ions. The role of adduct formation, steric hindrance, as well as the nature of the bonding atom in the chelate ring, represent some of the factors affecting selectivity arising out of our database of over 200 individual extraction systems, which will be discussed.

Jan 1, 1989

By Jakub Kaczorowski

In the production of Mn-alloys, the Boudouard reaction significantly influences the mass and energy balance. The endothermic nature of this reaction requires more energy for the process, while the direct consumption of carbon is reflected in the greater demand for carbonaceous raw materials. Therefore, it is desirable to eliminate or suppress the reaction. The kinetics of the Boudouard reaction are a function of many factors, of which coke properties and the conditions around the particles (i.e. temperature, gas composition) seem to be the most important. In the present study properties of selected single source and commercial metallurgical cokes are compared with reactivity results. The single source cokes represent a single coal that has been carbonized in a laboratory scale furnace. The commercial cokes are products of carbonization of coal blends under industrial conditions. The coke properties include proximate, ultimate and ash analysis. Also, coke petrography with carbon forms is included. The reactivity tests were performed on different particle sizes at various temperatures, gas compositions and gas flow rates. The experimental parameters were chosen to simulate the conditions in an industrial furnace. The results show that highly graphitized structure of cokes, minimal surface area and a low concentration of ash retard the reactivity. Of the other factors, the temperature and the gas composition have the greatest impact on the reactivity.

Jan 1, 2006

By M. I. Kalashnikova

The leaching of metal nickel in copper sulfate solutions is investigated. It is established, that irre-spective of presence or absence of chloride-ion and oxidizer (oxygen) in system process can be divided into three stages, characterizing by restoration and oxidation of metals with formation of metal copper and cuprite and differing in the speeds of sedimentation of copper and transition of nickel into solution. At the initial stage of process along with allocation of metal copper it is be-sieged cuprite, that results in excess of speed of sedimentation of copper in comparison with dis-solution of nickel. At the second stage speed of transition of nickel into solution falls practically to zero, and sedimentation of copper proceeds on reaction of interaction of metal copper with copper sulfate solutions with cuprite formation. During the final period speed of transition of nickel into solution exceeds speed of sedimentation of copper due to course of reaction of resto-ration of cuprite up to metal. Influence of an ion of chloride and oxidizer on formation of various phases is revealed. It is established, that presence of an oxidizer results in increase in a share of cuprite in a deposit. With increase of the maintenance of chloride-ion speed of metal copper allo-cation essentially grows even at presence of an oxidizer in system.

Jan 1, 2006

By V. V. Kutumbarao, M. T. Nimje, G. Balasubramanian

Wastes from the aluminium industry such as red mud from the alumina refinery, fly ash from the captive power plant and spent pot lining from the smelter, have been successfully converted into glass-ceramic products. The process involves addition of a small quantity of glass former along with traces of nucleating agents to aid crystallization, to a specific mixture ofred mud, fly ash and spent pot lining, followed by melting at around 1300°C and vitrification by cooling. The resultant glass is then converted into a glass- ceramic by a suitable heat treatment at around 700 - 750°C. The glass-ceramic products show excellent wear resistance, besides possessing an aesthetic appearance. The major application foreseen for such products is as decorative tiles in the building industry.

Jan 1, 2000

By Xu Zhong

The theoretical limit to smelting rate and possibly the size of a smelter is dependent on the rate of heat transfer, and the chemical kinetics of both sulfur removal and minor element volatilization. The fundamental kinetics of volatilization of minor elements such as As, Sb, Bi, and Pb from matte and white metal is being investigated. It has been shown that the molecular form of trace elements in matte depends on the chemical potential of sulfur and the propensity for the minor element to form a sulfide. The impact of the variable molecular form of the minor elements on the volatilization kinetics is unknown and is under investigation in this study. The experimental technique is reviewed and preliminary results are reported in this manuscript.

Jan 1, 1995

By Corby G. Anderson

Today, with a stringent economic and environmental climate prevailing in the copper business, there is increased interest in evaluating new processing alternatives for production. Hydrometallurgical pressure oxidation of copper concentrates is one of the more viable approaches and several technological candidates have emerged. Of these, an overlooked but industrially proven methodology utilizing nitrogen species catalyzation in the oxidizing pressure leach system may prove to be a feasible process alternative for the future. In this paper, the history of the system and its application to chalcopyrite concentrates will be outlined. In particular, a methodology for effective treatment of precious metals bearing chalcopyrite concentrates via partial oxidation at low temperatures and pressures will be discussed. Finally, the perceived economics of this unique industrially proven process will be delineated.

Jan 1, 1999

By Ying-Chu Hoh

The extraction of cerium(IV) by valence change with two-phase electrolysis was studied experimentally. The results show that the electro-oxidation extraction depends mainly on the distribution of the solute between the two phases, the reaction on the electrode surface and the diffusion of the reactant and product between the electrode and aqueous interphases. The effects of various parameters on cerium extraction were also studied. The selected parameters were background current, catholyte acidity, agitation speed, operation current and voltage and surfactant addition. The electro-oxidation extraction mechanism can be divided into eight steps. In addition, Wee the rate of extraction is quite fast, the percentage extraction Ce+4 can be taken as an index to show the conversion rate of Ce+3 J to Ce+4.

Jan 1, 1989

By P. Regan

Following the introduction of the Contilanod process over 10 years ago at Copper Range and IMI Refiners, significant changes and advances have been made to this pioneering anode production technique. A new radial flow metal feeding concept has been developed that allows a substantial increase in casting rates on the Hazelett® twin-belt caster. To cut the 45 mm thick continuous anode plate into shaped anodes at rates of 100 t/h or more, a filly moving hydraulic shear designed by Mannesmann Demag has replaced the slower speed plasma cutting torch. Details of the.new caster and shear are presented along with operating results from the new lines starting up in 1999 at the Gresik smelter/refinery in Indonesia and the completely revitalized Mansfelder Kupfer und Messing complex in Germany.

Jan 1, 1999

By C. T. Yavuz

Higher environmental standards have made the removal of arsenic from water an important problem for environmental engineering. Iron oxide is a particularly interesting sorbent to consider for this application. Its magnetic properties allow relatively routine dispersal and recovery of the adsorbent into and from groundwater or industrial processing facilities; in addition, iron oxide has strong and specific interactions with both As(III) and As(V). Finally, this material can be produced with nanoscale dimensions which enhance both its capacity and removal. The objective of this study was to evaluate the potential arsenic adsorption by nanoscale iron oxides, specifically magnetite (Fe3O4) nanoparticles. We focused on the effect of magnetite particle size on the adsorption and desorption behavior of As(III) and As(V). The results show that the nanoparticle size has a dramatic effect on the adsorption and desorption of arsenic. As particle size is decreased from 300 nm to 12 nm the adsorption capacities for both As(III) and As(V) increase nearly 1000 times. Interestingly, this increase is more than expected from simple considerations of surface area and suggest that nanoscale iron oxide materials sorb arsenic through different means than bulk systems. The desorption process however, exhibits some hysteresis with the effect becoming more pronounced with small nanoparticles. This hysteresis most likely results from a higher arsenic affinity for magnetite nanoparticles. This work suggests that magnetite nanocrystals and magnetic separations offer a promising method for arsenic removal.

Jan 1, 2006

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 R. M. Nadkarni

This paper examines the broad' economic parameters of copper smelting by conventional and new smelting technology. Location, transportation of products to market and pollution control options are discussed.

Jan 1, 1983

By Hiroyuki Sano

Elimination of heavy metals from the incineration fly ash by the chlorination volatilization method had been already developed and the effectiveness of this method was confirmed by the present authors. In this study, this method was applied to the elimination of heavy metals, mainly lead, from the incineration bottom ash. Since the fly ash contains a large amount of chloride, heavy metals in the fly ash are easily chlorinated. On the other hand, the addition of the chlorination agent is a key point for applying this method to the bottom ash, because it hardly contains chloride. The effects of various variables such as a kind of chlorination agent, adding quantity of it and temperature on the elimination ratio were investigated and the harmlessness of the residual ash was evaluated. The preferable condition was proposed from the recyclability of the bottom ash.

Jan 1, 2006

By Fumito Tanaka

The Converting Furnace (C-furnace) of the Mitsubishi process has solely provided opportunities for producing blister copper continuously from molten matte. Continuous converting originates from the proven technology for controlling the behavior of magnetite in lime-ferrite slag of the CaO-FeOX-Cu2O system. Recent improvements in the C-furnace operation have included the slag controls reflecting the impact of minor oxides on magnetite behavior. Although previous investigations focused on magnetite behavior, sulfur has also affected the C-furnace operation because it is of practical importance to avoid the precipitation of gypsum from lime-ferrite slag and the separation of matte from blister copper. This paper will quantify the behavior of sulfur in C-furnace with respect to the gypsum formation and matte separation, and discuss better controls for C-furnace operation.

Jan 1, 2006

By Chai Li-yuan

Anodizing behaviors of magnesium alloys AZ31 at constant applied current, based on the electrolyte solution free of chromate or fluoride, were investigated. The anodizing process was influenced by constituents of electrolyte greatly. Therein, the oxylate salts, which led to the occurrence of the two totally different processes, played a determinant role in anodizing. They were stable and sparking process respectively. The morphology of anodizing film was observed by SEM and the structure of film was analyzed by XRD. During the stable process, a brown thin film was formed, however the sparking process led to the formation of white hard thick film. The functions of some kinds of additives, such as ammonia, glyceryl alcohol and PVP etc were also studied. Some of them had great effect on surface morphology of anodic film and some of them affected stability of anodizing process significantly.

Jan 1, 2006

By Jay Black

In the thiosulfate gold leaching process gold is oxidized to Au+ by a copper(II) ammine catalyst and complexed by thiosulfate. Copper(I) complexes, formed during gold oxidation, are reoxidised to Cu(II) complexes by oxygen. In this study, we present the results of a spectrophotometric study of the Cu(I)-NH3-Cl system, which follows on from our recent investigations of speciation in the Cu(I)-Cl and Cu(I)-S2O3-Cl systems and is part of a detailed study of copper(I) speciation associated with the gold leaching process. Formation constants for Cu(I)-NH3-Cl complexes have been determined by modeling the systematic changes in the UV spectra that occur as the concentration of the components is varied. The analysis of the data indicates that three Cu(I)-ammonia complexes are present, i.e., [Cu(NH3)2]+, [Cu(NH3)Cl2]- and [Cu(NH3)2Cl] and their respective log Kf values are 11.13, 8.33 and 10.79 at 25°C. Investigations of the oxidation of Cu(I)-NH3-Cl solutions by oxygen in the atmosphere are also presented. These experiments indicate that the reaction of copper(I) complexes progresses through various intermediates. The presence of many copper(I) and copper(II) complexes in ammonia thiosulfate solutions complicates the task of determining optimal conditions for gold leaching. Further studies are needed to identify the complexes and chemical processes that are important in the Cu(I)-NH3-S2O3-Cl system.

Jan 1, 2003

By T. T. Chen, J. E. Dutrizac

Noranda Inc., CEZinc presently employs a cement-stabilization (jarofix) process to stabilize its jarosite residues for direct disposal. In this process, Portland cement partly decomposes Na-jarosite to form Ca6Fe2(SC>4)3(OH)i2.nH20, ferric hydroxide and sodium sulphate which further reacts to form gypsum; approximately one-third of the Na-jarosite reacts in the current commercial product. The cured jarofix products also contain minor amounts of various Ca-Al-Fe silicate-sulphate-hydrate phases and traces of calcite. Together with gypsum and a Ca-Fe sulphate phase, these species bond the various particles together, imparting mechanical strength and reducing the permeability. Water-soluble Zn and Mg are stabilized in the Ca-Al-Fe silicate-sulphate-hydrate phases. The freshly cured products usually contain small amounts of moisture and traces of residual Portland cement, which provides additional alkalinity for the neutralization of any residual acid species. Jarofix products stored for more than six years in the laboratory, after curing, are usually dry and exhibit the same micro-textures as those of the freshly cured products. However, the stored products are depleted in the Ca6Fe2(S04)3(OH)i2.nH20 and Portland cement phases, and are enriched in gypsum and calcite which reflects the highly alkaline environment of the jarofix products. The aged products also have increased amounts of the Ca-Al-Fe silicate-sulphate-hydrate phases which have elevated Zn and Mg contents. This implies a further immobilization of residual water-soluble Zn and Mg during stora

Jan 1, 2000