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By KNona Liddell

Many metal recovery processes Involve heterogeneous reactions In porous media accompanied by fluid flow and mass transfer. Modeling such systems Is difficult because of the number of rate processes Involved and is complicated even further by effects due to the structure of the porous medium. Data on even bulk properties of the medium are often severely limited or unavailable. For many such systems, a cell model may provide, an attractive alternative to models based on transport ,mechanisms in a differential volume. A cell model requires less input data and is computationally efficient. Identical residence time distributions can be obtained with models of both types, and both allow conversion and concentration profiles and histories to be calculated. The formulation and properties of cell models for metals recovery are described in detail.

Jan 1, 1996

By C. K. Gupta

Electrometallurgical processes have a definite place in the extraction technology of rare earth metals and alloys. Some of the advantages of the molten-salt electrometallurgical processes include fast electrode reaction, providing accurately controlled large amount of energy to a relatively small reactor volume, negligible over voltage, simplicity of operation, and possibility of accomplishing continuous or semicontinuoue operations. This paper provides a vivid account of the theoretical and practical aspects of electrometallurgical processes for the production and processing of some of the rare earth metals and alloys. Reference has been drawn to the work reported on electrometallurgical processes as applied to the preparation of lanthanum, cerium and misch metal from author's laboratory.

Jan 1, 1992

By V. Jiricny

The novel spouted-bed electrode (SBE) is a cathode system where copper is deposited at a high current density in a moving bed of copper particles. Preliminary results on the deposition of copper from acidic sulfate electrolytes using this novel cathode system were described during Copper '95 conference. Despite a high current density, the electrical energy consumption was equal to or lower than that in the conventional electrowinning. The present paper describes more investigations on SBE. The SBE consists of copper particles with approximately 1 mm diameter onto which copper is deposited from acidic sulfate electrolyte whose composition is similar to conventional electrowinning. Three types of anodes were used in conjunction with the spouted-bed cathode, namely, DSA anode for oxygen evolution, and two novel anodes. One anode is less expensive than DSA; however it showed much promise in energy consumption. At a superficial current density of 2200 A/m2, the energy consumption was around 1.0 kWh/kg copper. The research activities described in this paper were supported by BHP Copper.

Jan 1, 1999

By Yanping Xiao

In submerged-arc furnace (SAF) for smelting chromite ores into ferrochrome, there exist large temperature gradients and wide distributions of mineralogy and compositions in the furnace, due to the complexity of feed structure and electrical-thermal-chemical interactions. This leads to various zones in the furnace and thus different reaction mechanisms. In the present paper, the behaviour of chromium in the submerged arc furnace is discussed in various reaction zones, including solid state chromite reduction in the packed bed zone, chromite dissolution and reactions in the smelting and coke bed zone, and recovering chromium from slag to metal. In the gas-solid reaction zone, the reaction mechanism is discussed based on the experimental observations and analysis. In the smelting zone, the behaviour of partially reduced chromite and slag formation are analyzed based on the information in literature. The slag in FeCr process contains mainly Al2O3, MgO, SiO2, CaO and CrOx, featured by chromium with both divalent and trivalent oxidation state, which plays an important role for chromium recovery into metal. The factors influencing the slag and metal interfacial reactions and the chromium recovery are addressed.

Jan 1, 2006

By Serdar Aksu, Fiona M. Doyle

"CMP will be an essential process in the production of integrated circuits containing copper interconnects. This study aims to improve our mechanistic understanding of the role that organic chelating agents might play in the reactive slurries used in copper CMP. Copper dissolution behavior in EDTA arid glycine was first examined by producing potential-pH diagrams for the copper-water-EDTA and copper-water-glycine 'systems. The results of potentiodynamic polarization experiments were then considered in light of these diagrams. . In-situ polarization experiments were conducted to gain insight into the electrochemistry of copper during dynamic polishing in slurries prepared from EDT A and glycine.IntroductionCopper has recently started to replace aluminum as the interconnect metal in integrated circuits. Copper interconnection offers faster and more reliable integrated circuits due to its higher electrical conductivity and superior electromigration resistance (1). The damascene method is used to form multilevel interconnects in the manufacture of integrated circuit devices with copper metallization (2, 3). Copper is deposited by CVD or electroplating into vias and trenches etched in the interlayer dielectric (IDL), over a diffusion barrier usually made from titanium, tantalum or their nitrides. Chemical mechanical planarization (CMP) then prepares the wafer for the next deposition step, by removing excess copper and planarizing the surface. During CMP, the wafer is rotated and pressed against a rotating platen covered with a polishing pad. Chemically active slurries containing submicron size abrasive particles (Si02, Al20 3, ceria, diamond, etc.) are applied. Both the mechanical action of the abrasive particles and the chemical action of slurry constituents remove material from the wafer surface. Planarization results because material is removed faster from protruding regions on the surface than from recessed regions. Since CMP can globally planarize .the entire wafer, it has become one of the key technologies for producing integrated circuits with copper metallization."

Jan 1, 2000

By Leszek Hoser

Polycrystalline oxide superconductors that have the perovskite structure, that are oxygen deficient, and that have compositions based. on the so-called. 1-2-3 (YBa2Cu3O7) compound, were investigated.. The materials exhibit a high critical transition to superconductivity at temperatures near 90oK. It was determined that maintaining the oxygen content within the correct range in connection with an appropriate amount of CU ions in the crystal lattice leads to high-critical temperature (Tc:) superconducting properties. High-Tc: superconductors with a critical temperature in the range of 100°K were developed. Further investigations, based. on the theoretical examinations of the origin of superconductivity, have been performed and are discussed..

Jan 1, 1989

By Pekka Taskine

In the Kokkola zinc smelter, as in most other zinc roasting plants, there is now a trend towards using concentrates with an increasing impurity content. This also often means that the size distribution of the concentrates gets finer. Iron is present in sulfidic zinc concentrates with the highest percentage as a single impurity. The behavior of iron in zinc roasting was studied in laboratory experiments. Commercial zinc concentrates with a low and high (1.5 - 16 wt-%) iron content as pyrite or in the sphalerite lattice were oxidized to various degrees to establish the reaction mechanisms of iron in roasting. Microscopy studies were carried out on the calcine, and the findings were presented in numerous photographs of the polished cross sections. SEM/EDS techniques were used for analyzing the phases and particle morphologies present in the samples. An oxidation mechanism of zinc concentrates with a high iron content was suggested.

Jan 1, 2002

By M. Hashiuchi

In 1972, the tankhouse of the Tamano Smelter adopted a high current density electrolysis operation applying the PRC (Periodic Reverse Current) method. In 1994, the phase four production expansion project, which incorporated significant re-structuring of the organization, was completed and we have achieved an annual production capacity of 191,000 tons. The target of this project, the production capacity, was increased by 1'8% and labor productivity by 25%. After the expansion, some improvements in the starting sheet section and the verticality of the electrodes were carried out, and the efficiency of the operation was greatly enhanced, including the improvement of the quality of the electrolytic copper.

Jan 1, 1999

By Jari Aromaa, Olof Forsen

"Oxygen evolution by decomposition of water is the main anodic· reaction in sulphuric acid solution. Traditional anode materials have been relatively low-cost lead alloys, though the active lead dioxide layer has a high oxygen evolution overpotential. This causes a significant increase of cell voltage. To lower total energy use in metal production, electrocatalytical properties or corrosion resistance to decrease replacement costs must be improved. Addition of an catalyzing ion will decrease oxygen evolution potential. The effective area of an anode increases by calcium additions and by producing anodes with fine microstructure. Remelting and rapid quenching is possibly a method that is economically feasible and technically simple enough to be adopted.IntroductionPermanent anodes are widely used in several electrochemical processes and cathodic protection applications. The permanent or ""inert"" anodes can be either massive or coated anodes. The massive anodes are metals, like lead alloys, or non-metals, like magnetite, graphite or ferrite. The coated anodes are made of a valve metal base (titanium, niobium or tantalum) coated with an electrochemically active coating. The purpose of anodes is to supply current to the electrochemical cell. A vast number of materials and their combinations are electrical conductors and may hence be used as anode materials. However, good anode materials must survive in aggressive environments and also be able to pass high current densities. These opposite requirements restrict the amount of possible materials. Generally, an useful anode material must meet three requirements, electrical conductivity, electro catalysis and stability. Good electrical conductivity is essential for energy efficiency. Good electrocatalytical properties are essential to improve product yield. Long term stability is also an important property, because electrode wear and corrosion may cause product contamination, increasing energy consumption and material and labor costs due to need of periodical maintenance. Electrical conductivity and electrocatalytical properties are more widely studied subjects than long term stability of anodes, and a good amount of information about these two subjects can be found in the open literature. Wear and corrosion mechanisms of the anodes vary depending on the operational conditions, i.e. concentration of different species, temperature and operating current density."

Jan 1, 1997

By N. Krishna

The utilization of Electrochemical Impedance Spectroscopy (EIS) in conjunction with Atomic Force Microscopy (AFM) is a powerful surface characterization technique to study the role of sulfur formation during acidic oxidation of chalcopyrite. It has been established that the chalcopyrite dissolution kinetics is controlled by the formation of passive sulfur layer during leaching. The objective of the study was to characterize the intermediate sulfur layer formation at different oxidation conditions in acidic solution. The chalcopyrite samples were subjected to anodic oxidation and the oxidation process was analyzed using impedance spectroscopy. The sulfur growth on the chalcopyrite surface during oxidation was further analyzed using Atomic Force Microscope for sulfur roughness and grain size, peak height and sulfur growth.

Jan 1, 1999

By J. Alberto Vázquez M.

A sensor employing yttria-stabilized zirconia (YSZ) was used to determine the oxygen activity of molten copper at laboratory scale at temperatures of 1200° and 1300 dc. The reference electrode was a Ni-NiO mixture. The amount of the deoxidizing agent (CU3P) ranged from I to 3% of the mass of copper. Thermodynamic analysis of the Cu-O-P liquid system was carried out to predict the required deoxidizing agent and the final composition of the molten copper. Both results, calculated and experimental, show that the oxygen removal is more efficient at lower temperatures. The kinetics of the deoxidizing reaction is very fast in the first minutes of the treatment. A metalography analysis of rapid cooled samples show the oxygen and phosphorus distribution

Jan 1, 2003

By Grigore Matei

The thermodynamic properties of CuzS-FeS system are important not only in the ease of copper smelting but also in the case of general pyro-metallurgy. However there arc not many reported activity data In this study, activities of FeS and CU2S in the Cu2S-FeS system were calculated using the Darken's method from the activity data of the Cu2S-FeS-Sb2S3 systems measured by the transportation method at 1050°C. The activities of Cu2S and FeS in the Cu2S-FeS system showed negative deviation from the ideal behaviour and satisfied the relation of the Gibbs-Duhem equation.

Jan 1, 2003

By Kimio Itagaki

The distribution ratios of Ag, Pb, As, Sb and Bi for the Cu2S-FeS or Ni3S2-FeS matte / FeOx SiO2, FeOx-SiO2-CaO or FeOx-CaO slag equilibration in a MgO crucible were determined experimentally at 1523~1573K under controlled partial pressures of S2 and O2 at given PSO2 of 10.1, 50.7 and 101.3 kPa (0.1, 0.5 and 1 atm) and be observed dependency of distribution ratio on the matte grade, SO2 pressure and slag basicity were analyzed on the basis of thermodynamics,

Jan 1, 2003

By Daniel Kim, Justin McAllister, Shijie Wang

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

Jan 1, 2012

By G. A. Brooks

Reactive ball milling has been proposed as a new route for producing carbides from oxides through carbothcrmic reduction. It is claimed that through milling oxide and graphite powders to the nanoscale, amorphous materials with very high reactivity are formed, that allows for easy transformation of the starting material to another in a subsequent thermal process. Thermodynamic analysis of this proposed process suggests that unless particle sizes are reduced to below 10nm, then reduction in size alone cannot explain a change in the stability of oxides. Even with nanometer scale powders, the products formed need to have a lower total surface energy than the reactants before a chemical change will occur. A model developed by Bhattacharya and Arzt for predicting localized temperature changes based on milling conditions suggest that temperarure rises less than 400 K will be achieved in laboratory conditions. The present calculations suggest that nanometer scale powders formed through high speed ball milling (>10 mls) may have undergone a process analogous to melting and quenching. Further work is required to fully distinguish these features.

Jan 1, 2003

By Roger N. Kust

Removal of heavy metals from industrial process streams is becoming increasingly important for _the recovery and reuse of values in process tails. Technology has been available for several years which removes heavy metals, from dilute (0.1-3.0 g/L) streams, as hydroxide or hydrated oxide sludges, allowing discharge of washed cakes with up to 60% solids. This paper reports on improvements to this technology which now allows treatment of streams with metal concentrations in excess of 60 g/L while eliminating the need for thickeners. Streams containing copper, iron, aluminum, chromium, nickel, zinc, cobalt and lead have been successfully treated.

Jan 1, 1992

By Dale T. Peters

In the United States, the United Kingdom and numerous other countries, copper has long been the plumbing material of choice. This has been the case since the late 1920s in the United States and since World War II in the United Kingdom. However, in recent years the plumbing tube market has caught the eye of the chemical industry, and several plastic resins have been introduced to the marketplace as substitutes for copper in household plumbing systems. One of these, polybutylene tube, had so many failures in the United States that a class action law suit was filed, and the manufactures of this product were forced to create a trust fund of nearly one billion dollars to repair damages caused by their product. Chlorinated polyvinylchloride (CPVC), in rigid pipe form, on the other hand, has been mechanically acceptable albeit its recent introduction precludes the test of time enjoyed by copper tube in this application. This paper reviews the State of California's portrayal of copper's environmental effects and will be largely based on the data and information assembled by the Copper Development Association Inc. in its presentation to the State of California in August, 1998 in response to the State's Draft Environmental Impact Report for Chlorinated Polyvinyl Chloride (CVPC) Pipe for Use for Potable Water Piping in Residential Buildings. The paper is intended for use as a model for the use of other copper organizations and individuals in responding to similar situations.

Jan 1, 1999

By Larry M. Southwick

Pneumatic converting (Bessemerizing) of iron revolutionized the steel industry. Bessemerizing of copper (conversion of copper sulfide matte to copper metal) was proposed at almost the same time, but it was slow in being accepted. The differences between iron and copper converting were great and technical problems were substantial. It took 25 years for the process to become viable and another 25 years before a truly economical solution was found. A major economical and productivity problem was the short life for converter refractory linings. The first converters had acid (silica) linings, which were quickly consumed since silica was a flux for the process. Converters had to be relined at least once per day, a laboriously expensive manual process with only the most rudimentary mechanical aids available to assist. The industry was revolutionized almost overnight when finally a viable basic (magnesite) lining was developed. This lasted 100's of days versus less than one, leading to converters that were easier to operate and which handled larger charges. This change occurred after W.H. Peirce and E.A.C. Smith, with support from the Guggenheim interests, successfully operated a basic lined converter in a copper refinery in Baltimore. While Peirce and Smith are generally given credit for the development and explosive acceptance of this idea, a Pittsburgh industrialist, Ralph M. Baggaley, working in an independent smelter in Butte, Montana, successfully built and operated a basic lined converter four years before they did. In fact, the early support for Peirce and Smith likely occurred because Guggenheim's staff were encouraged after thoroughly examining Baggaley on his earlier successes. The questions of technology primacy between Baggaley and Peirce/Smith are ironically similar to those between Wm. Kelly and Bessemer in converting iron to steel. This paper will review what Baggaley (and other early researchers) accomplished, examine why he (or they) did not receive credit equal to Peirce and Smith and explore what his (their) place should be in the development of successful basic linings. More suspects than a Victorian Whodunit.

Jan 1, 1999

By J. C. Agarwal

Do large-scale projects in mining and smelting start up and achieve expected capacity on schedule? In most cases not. Regardless of worldwide location, company know-how, or financial backing, unforeseen delays occur. A comprehensive CRA study for the World Bank shows that delays are the rule, not the exception, in most mining and smelting projects. When delays are not factored into analysis and planning, financial projections are, literally, not to be believed. Returns on investment will seldom achieve their targeted level because of startup delays. This paper reviews the results of our analysis of startup of new mines, mills, and smelters; provides a detailed discussion of why delays occur in the smelters and refineries; presents the cash flow implications of startup delays; and discusses preventive measures that should be taken to avoid financial shortfalls,

Jan 1, 1983

The kinetics of the oxidation of cyanide by manganese dioxide was studied using a rotation disc electrode system. The rate? of the half-cell reaction of cyanide oxidation is increased at higher hydroxide concentrations. An addition of copper up to 0.001 mole/l was found to enhance the diffusion current, especially at a high hydroxide concentration (0. 1M). A similar enhancement of the reaction rate is also achieved with nickel added at levels up to 0.01 mole/l. Manganese dioxide however requires a i:ow pH to achieve reasonable reduction rates. Leaching studies indicated that the initial reaction rate is strongly dependent on pH, initial concentration of cyanide. Using manganese dioxide cyanide could be oxidized at neutral pH's and ambient temperatures.

Jan 1, 1989