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By Kang-In Rhee

Nonferrous metal recycling not only provides energy saving and environmental benefits but also is a significant factor in the supply of various types of metals used in our society. Recycling plays an important role in establishing the sustainability of materials. The total amount of recycled nonferrous metals by weight accounts for less than 5% but their value is larger than 50% compared to ferrous metal recycling which consists of about half of the total metal recycling in weight. This paper describes trends and typical achievements in nonferrous metal recycling and overviews the present and future of nonferrous metal recycling technology and business in Korea.

Jan 1, 2006

By Sergio Demetrio

Over a period of nearly a hundred years throughout this century, the company direction and management of copper smelters in Chile has evolved from one characteristised by a paternalistic, autocratic style to one which empowers the local management team and people for running the smelter as a successful business. This paper discusses the evolution of the present style of management amidst changes in the Chilean Government, the mining industry and society since the beginning of this century.

Jan 1, 1999

By James A. Sommers

Combustion of niobium nitride powder in a stream of oxygen results in several niobium oxide phases, depending upon reaction parameters. Under rapid oxygen flow, the oxidation produces a molten mass which coalesces into droplets of ca. 2 mm dimension and effectively quenches to leave NbO2 and other lower oxides of niobium, despite the ambient atmosphere of oxygen. A preliminary survey of reaction parameters which govern the split between reduced and oxidized products is presented. This technique offers novel synthesis means for binary oxides when mixtures of NbN and other materials are combusted together, since the niobium moiety is generated in a molten state.

Jan 1, 1995

By M. F. Chambers

Neodymium metal was electrowon from a molten-chloride electrolyte at 650° C using a molten-metal cathode. A 50 mol pct NdC13-50 mol pct KC1 mixture served as the electrolyte. Binary metal alloys of 'Mg with Zn and Mg with Cd were used as molten cathodes. Under the best conditions, current efficiencies were 90 pct with a Mg-Zn cathode and 80 pct with a Mg-Cd cathode. Vacuum distillation was performed at 1,100° C for 30 min under a vacuum of 10-3 to separate the cathode metals from the neodymium. Neodymium metal of 99.9+ pct purity was recovered from the Mg-Cd alloy cathode. Almost 2 pct zinc remained in the neodymium recovered from the Mg-Zn alloy.

Jan 1, 1989

By Corale L. Brierley

Bioheap leaching, commercially applied for secondary copper ores and agglomerates, is rapidly gaining popularity. Bioleaching of chalcopyrite concentrates is imminent. Copper bioheap leaching encompasses the bioleaching of acidified and agglomerated coarse, secondary copper ore, stacked on permanent or on/off pads. The stacked ore is irrigated with raffinate containing bacteria. LME-grade cathode copper is produced by SX/EW. Low capital and operating costs, rapid start-up, environmental benefits, operational simplicity and a good performance record make bioheap leaching an attractive technology. This paper looks at the state-of-the-art of copper bioheap leaching and chalcopyrite concentrate leaching, the risks, the benefits, costs, bioheap performance and the future prospects of copper bioleaching.

Jan 1, 1999

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 E. Gervais

Modern life in inconceivable without zinc. Zinc provides the most cost-effective and environmentally efficient method of protecting steel from corrosion. Zinc is also used to power electric vehicles and computers, to make brass, automotive equipment, household appliances, fittings, tools and toys, and to support the building and construction industries. It is also used in pharmaceuticals and cosmetics, in rubber, in fertilisers and in animal feeds. The links between properties, applications and performance, as well as zinc demand and market dynamics, will be reviewed along with market development opportunities and successes. The presentation will also include a progress report on the five-year plan of the International Zinc Association to increase the global market for zinc, over and above the natural growth, by 500,000 tonnes/year by 2002.

Jan 1, 2000

By Robert L. Opila

Negative electrodes for alkaline nickel-metal hydride batteries composed of MmNi3.5Al0.8Co0.7, where Mm is misch metal, have been characterized electrochermically and using x-ray photoelectron spectroscopy. The stability and rapid hydriding and dehydriding kinetics of the alloy in KOH are attibuted to a surface film. The protective surface film is shown to consist of an porous, outer hydrated layer and a dense, inner oxide layer. In addition, metallic nickel and cobalt are found throughout the film, and are presumed to form a conductive, percolative network that permits rapid electron transfer from the bulk to the solution, allowing rapid electrochemical formation of atomic hydrogen.

Jan 1, 1997

By Corby G. Anderson

Over the past 15 years, numerous pressure oxidation plants for pretreatment of gold ores and concentrates have been installed throughout the world. While this technology is now established, it suffers in terms of the complex engineering and operational characteristics inherent in utilization of high temperatures (i.e. up to 225oC) and high pressures (i.e. > 3000 kPag). This paper outlines the application of an industrially proven pressure leaching methodology utilizing nitrogen species catalyzed pressure leaching and alkaline sulfide gold leaching. As such, it stands as an economic and engineering advancement in pressure leaching and non-cyanide treatment of gold ores and concentrates. In particular, the technology offers significant technical and economic advantages over traditional pressure oxidation and cyanide gold recovery in the treatment of gold bearing chalcopyrite ores and concentrates. An example of this will application will be delineated in this paper.

Jan 1, 2003

By Giovanni Principi

The activity of the ?Hydrogen Group? of Padova University, addressed to the study of materials for solid state hydrogen storage, is illustrated. Various Mg-based materials have been considered and are being studied: a) MgH2 and 0.5% mol Nb2O5 mixture ball milled under argon atmosphere; b) Mg-Ni-Fe intermetallic compounds prepared by short time ball milling of ribbons obtained by melt spinning and by long time ball milling of a mixture of MgH2, Ni and Fe powders; c) MgH2 ball milled in argon with Mm-Ni-Al (Mm = La-rich mishmetal) and Zr-Cr-Fe catalyst alloys. All the samples have been structurally characterized by X-ray diffraction (Rietveld refinement) before and after hydrogen absorption/desorption cycling and tested with a Sievert apparatus as regarding their thermodynamic and kinetic properties.

Jan 1, 2006

By N. Choi

The distribution behavior of cobalt, gold, and silver in nickel sulfide smelting was investigated between 1250-1300 °C under inert gas atmosphere. The distribution coefficients of these elements between nickel-copper-iron matte and silica-saturated iron silicate slag were determined as a function of matte and slag compositions. The effect of slag additives such as CaO, MgO, and Al2O3 on the solubility of cobalt, gold, and silver in slag was also investigated. It was observed that the distribution coefficients of these &nor elements were strongly dependent on matte grade. For cobalt and silver, the distribution coefficients decreased as the matte grade increased. However, the distribution coefficients of gold increased as the matte grade increased. The solubility of these minor elements in iron silicate slag was considerably decreased by the addition of basic oxides. Temperature dependence of the distribution of the minor elements will also be discussed.

Jan 1, 1995

By Jun-ichiro Yagi

A mathematical model has been developed for simulating the blast furnace operation with carbon composite agglomerates charging based on multi-fluid theory and reaction kinetics. In this model, the behaviours of carbon composite agglomerates are considered on the basis of previously reported conservation equations and experimental research on the reduction rate of carbon composite agglomerates. A series of calculations are performed to examine the effect of charging carbon composite agglomerates. The model calculation gives two-dimensional distributions of process variables and information on the overall operational parameters. It reveals that in-furnace temperature levels significantly decrease and the reduction of carbon composite agglomerates is retarded with carbon composite agglomerates charging ratio. The furnace performance is remarkably improved with the increase in carbon composite agglomerates rate. The productivity tends to increase while coke rate and total reducing agent rate show decreases at the different degree.

Jan 1, 2006

By Michael J. Virnig

The formation of crud is a normal part of operating a solvent extraction circuit for the recovery of copper. It periodically must be removed from the circuit. This results in significant costs in terms of manpower, downtime, and loss of circuit organic. Field studies have been carried out that show that the presence of a thermodynamic modifier in the organic phase contributes to crud formation. In an effort to better understand what factors contribute to crud formation, laboratory studies involving competitive adsorption studies with model solids have been carried out. The results of these laboratory studies will be integrated with the results of the field studies to present a better understanding of crud formation.

Jan 1, 1999

A full-scale test of chalcocite heap bioleaching was undertaken at Straits? Nifty Copper Operation. Straits worked closely with the CSIRO to investigate the chemical and biological changes over the life cycle of this chalcocite heap bioleach system. Results indicated nearly 80% copper recovery was achieved in just over 300 days. Significant changes in iron chemistry and microbiological activity were detected. Temperatures in the heap reached as high as 70 ºC during the time of maximal copper recovery rate. The dominant cultivatable bacterial strains were typical mesophilic bacteria, however, naturally occurring moderately thermophilic bacteria were detected by culture and culture independent molecular (PCR followed by denaturing gradient electrophoresis [DGGE]) and signature lipid methods. Signatures for the iron and sulfur-oxidising species Acidithiobacillus ferrooxidans and Sulfobacillus spp., as well as the moderately thermophilic heterotroph Alicyclobacillus sp. were detected. Biomass was greatest in ?warm? but not ?hot? parts of the heap, and Hyperthermophilic Archaea were not detected.

Jan 1, 2003

By Michael J. Nicol

One of the preferred methods for the recovery of gold from refractory gold ores and concentrates involves pressure oxidation in acidic solutions. The main refractory gold-containing minerals are pyrite and arsenopyrite and there is evidence that the presence of even small amounts of chloride can inhibit the oxidation of these minerals and also substantially reduce the recovery of gold. In this paper, the results of a study of the anodic (oxidation) and cathodic (reduction) behaviour of pyrite electrodes in acidic sulfate solutions containing ferric ions at different chloride concentrations and temperatures up to 200oC and pressures of 2000KPa are presented. The electrochemical studies have been complemented by pressure oxidation experiments on a refractory gold concentrate. Results have shown that, as the chloride concentration increases, the anodic reactivity of pyrite is largely unaffected but the rate of the cathodic reduction of iron(III) decreases. The rate of oxidation of a sulfide concentrate and the recovery of gold by cyanidation of the residues decreases at high concentrations of chloride.

Jan 1, 2003

By Y. F. Jia

Arsenic constitutes a major contaminant for the hydrometallurgical industry. Its removal and immobilization from process effluents typically involves lime neutralization and co-precipitation with ferric iron (Fe (III)/As(V)>3). Alternatively, precipitation of scorodite (FeAsO4?2H2O (cr)) may be applied to arsenic fixation. The mechanism of arsenic fixation in the former process has been suggested to be surface adsorption. Unequivocal characterization of these products is difficult because of their amorphous nature hence a variety of methods need to be applied including the particularly powerful method, extended x-ray absorption fine structure (EXAFS) spectroscopy. In this study, we have investigated the preparation of arsenate-adsorbed ferrihydrite with the purpose to compare its structure to that of Fe(III)-As(V) co-precipitates and scorodite (both amorphous and crystalline). Furthermore the solubilities of these Fe(III)-As(V) solids are measured as a function of pH. Their structures are elucidated and correlated to their solubilities and thereby the application of these findings to the practice of arsenic removal and disposal is assessed.

Jan 1, 2003

By Michael S. Moats

As commercial copper electrorefineries look to expand their capacities by increasing their operating current density, the likelihood of anode passivation intensifies. To improve the industry?s understanding of the passivation phenomena, the role of anode composition was evaluated. While previous studies have focused on studying one impurity element at a time, this study was conducted using forty-four commercial electrorefining anode samples supplied by ten copper companies The passivation response of each sample was evaluated under accelerated galvanostatic conditions in synthetic copper electrowinning electrolyte at 65°C. This information allows for correlations between composition and passivation tendencies over a wide range of impurity elements and concentrations. It was found that selenium, tellurium, silver, lead and nickel accelerated passivation. It appeared that oxygen accelerated passivation when increased from 500 to 1500 ppm, but further increases did not have an effect. Arsenic was the only impurity found that inhibited passivation.

Jan 1, 2006

By Jeaneth S. Benedetto

The physical and chemical processes developed for recovery of uranium and phosphor from phosphoro-uraniferous ore bodies consists of three basic steps: concentration of the phosphate bearing uranium by flotation, chemical dissolution of the concentrate by wet phosphoric acid and extraction of uranium by solvent. In this process two products are obtained: 1) uranium and 2) phosphoric acid. The purpose of this work was to develop technological know-how of phosphoric acid purification though an extraction of P2O5 by solvents. It was investigated by two lines of research. In the first one the uranium was extracted before the phosphoric acid purification. In the second, the phosphoric acid was extracted before uranium recovery. The comparison of the two processes is shown in this paper. Experimental work was developed on a laboratory scale to select and optimize the process variables. After the laboratory study, the research of extraction and stripping was continued on a pilot scale in pulsed perforated-plate columns in order to investigate the main operational and process conditions. The first phosphoric acid extraction experiments showed good results using a raffinate sample obtained from the uranium extraction process. It was possible to obtain a high purity phosphoric acid.

Jan 1, 2003

By Celaletdin Ergun, Ibrahim Erden, Gurbuz Gunes, Thomas J. Webste, Huinan Liu, Abdurrahman Bahadll

"B, Ti, Ag, AI and Cu substituted hydroxyl apatites were synthesized via precipitation method. Then the samples were air-sintered at 1300°C for 2 hrs and characterized with XRD, SEM, FTIR, and cell adhesion behaviors.IntroductionSynthetic hydroxylapatite (HA, Ca10(P04)6(0H)2) has a similar composition and structure to biological apatite. Therefore, it has been safely and extensively used as an implant material for bone substitute. However, synthetic HA has been used for a various applications including medical or non-medical applications, such as matrices for drug release control, bone cements, tooth paste additive, blood purification agent, monolithic implants or coatings on metallic implants, packing media for column chromatography, gas sensors, catalysis and host materials for lasers and luminescent materials, etc. [1-9].The major factors affecting the performance of HA on these applications are crystal morphology, density, porosity, pore size and distribution, chemical composition, and surface structure. As provided by the high flexibility of the apatite structure a great variety of cationic and anionic species can be substituted into HA structure which is specifically considered as an effective method to modify the properties of HA [10,11]."

Jan 1, 2012

By C. Flores

The direct cementation of copper from a loaded D2EHPA 20 % vol. in kerosene using zinc, zinc-lead alloy and iron metallic powders was studied. Copper was loaded into the organic solvent from an aqueous copper sulfate solution. Results indicated that copper is reduced spontaneously with relatively fast reaction rates. The effects of several operating parameters such as water content in the organic system, initial copper concentration, reductant surface area, oxygen and nitrogen atmosphere, intensity of the agitation and temperature on the galvanic stripping of copper were studied. For a better understanding of the electrochemical reactions involved in the galvanic stripping, the dissolution of metallic copper in the organic solvent was also studied. Copper did not dissolve unless a small amount of water was present in the organic system. The results and possible reaction mechanisms are discussed.

Jan 1, 1999