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By J. F. Leroux

The Gaspé smelter at Murdochville, Quebec, Canada introduced concentrate injection into elongated Peirce-Smith converters sized 1.96m x 12.5m (13 ft. by 41 ft.) in 1996, and commissioned a large, converter-like bath smelting vessel in April 1998. The new vessel, which is sized 4.27m x 16.1 5m (14ft. by 53ft.) has several interesting features designed to effectively utilize bath smelting technology for the requirements of the Gaspé smelter. For example, the vessel can operate on concentrate injection at upwards of 60-80 tph rate on an instantaneous basis, can operate as a large Peirce-Smith converter, while it is also fitted with matte and slag tapholes much akin to Noranda Process reactor, and includes a novel cold charge addition system. The new technology will eventually allow the capacity of the plant to increase from about 300,000 tonnes of concentrate per year to over 350,000 tonnes of concentrate per year while improving sulfur capture.

Jan 1, 1999

By M. Ramprecht, M. Wu, A. Kharicha, A. Ludwig, H. Holzgruber

"The influence of the frequency of AC power supply on the magneto-hydrodynamic during the electroslag remelting process is studied. The focus is on the electrodynamic field and its resulting mechanical effects on the flow and liquid interfaces. The possible influence of the electrochemistry on the droplet formation is qualitatively discussed.IntroductionThe electroslag remelting (ESR) process is a secondary melting technique which can be used for a variety of metals and alloys, provided appropriate fluxes (slags) and melting parameters are employed. The ESR process is presently operating mostly with AC current of about 50 Hz. However for reasons primarily of inductive losses in the electric circuit, furnaces for ingots larger than 1 m, use or are projected to use current of very low frequency (< 5 Hz). Effects of lower frequencies (2.5-5Hz) on macrostructure and non-metallic inclusions were recently studied by Chang [1]. Most of investigations were performed either with DC power or with AC of 50-60 Hz [2-4]."

Jan 1, 2012

By R. E. Molnar

A number of flowsheets have been designed and operated, or are currently being considered, to extract copper from leach solutions having much more copper than the 4 g/L levels typically found in heap leach liquors. Dealing with these solutions has required that the envelope for ?normal? copper solvent extraction be pushed beyond the usually considered limits. Others have published information on flowsheets to recover copper from leach liquors containing over 25 g/L copper. Secondary solvent extraction circuits are often required to attain satisfactory overall recoveries. This paper reviews some of the issues faced in three pilot plant circuits that were operated by SGS Lakefield Research to produce cathode copper from solutions containing 8 to 20 g/L Cu. The primary objective was to maximize copper extraction using one solvent extraction circuit. The role of feed acidity and the disposition of impurities such as iron and chloride are considered. The challenges of running short SX piloting campaigns are discussed.

Jan 1, 2003

By Ali Akbar Mottahedi

Chromate conversion coating is a process for making a complex layer at the surface of zinc galvanized steel which makes the metal more resistant to corrosion, especially at marine atmosphere, and increases the adhesiveness of color. In this work the influences of various compositions on commercial zinc galvanized steel sheet to the color of chromate conversion coating has been investigated at normal temperature and the factors that affect the control and optimization of the process have been determined. A bath composition of 20 g/liter Cr203 and 10 g/liter NaOH and a dipping time of 50 seconds at room temperature (25-30°C) make a desirable color of chromate coating. A slow agitation at a constant pH of I (with additions of NaOH or H2SO4) assures a constant bath condition and develops the color. This kind of coating has more corrosion resistance and this bath condition and composition are also more economical.

Jan 1, 2003

By Do-Hyeong Kim, Tae-Jung Kim, Seung-Yeon Won, Jong-Jin Pak, Min-Kyu Paek

Liquid iron alloys containing V, Mo, and Ni can be produced by the carbothermic reduction of spent catalysts used in petrochemical industry. Thermodynamics of carbon in these alloy melts is important for refining these alloys. In the present study, the carbon solubility in Fe-V, Fe-Mo, Fe-Ni, Fe-V-Mo, Fe-V-Ni, Fe-Mo-Ni and Fe-V-Mo-Ni alloy melts of various compositions was measured at 1873 K. The temperature dependency of vanadium effect on carbon solubility in liquid iron was also measured in the temperature range from 1823K to 1923K. The additions of vanadium and molybdenum significantly increased the carbon solubility in liquid iron alloys while nickel decreased the solubility. The experimental results were thermodynamically analyzed using Lupis’ relation at constant activity to determine the first- and the second-order interaction parameters of vanadium, nickel and molybdenum on carbon at carbon saturated condition. Using thermodynamic parameters determined in the present study, the carbon solubility in Fe-V-Mo-Ni alloy melts of various composition were accurately predicted and verified experimentally at 1873 K.

Jan 1, 2014

By Jun Li

Several metal sulfides were examined in-situ by Raman spectroscopy before and after anodic oxidation. Results obtained for chalcocite, chalcopyrite, covellite, galena, pyrrhotite and pyrite electrodes are presented. Under appropriate conditions, sulfur was detected after a potential was applied to the mineral electrodes for a threshold period of time. For all the minerals, application of a negative potential on the oxidized mineral reduced the surface product and the sulfur peaks disappeared from the observed spectra. For those minerals containing sulfur as S< in the crystal lattice, polysulfides were identified as oxidation intennediates.

Jan 1, 1993

By Chuang Y-Y

A summary is made on the thermodynamic analysis for two of the four ternary systems of the quaternary Cu-Fe-Ni-S. The analysis is being extended to ternary Cu-Fe-S and then to the quaternary. An analysis is already made for the metal ternary but is not reported here. Experiment is being carried out to measure the liquidus surface. of Fe-Ni-S equilbrium with the fcc solid solutions of (Fe, Ni). The presentation at the Symposium will include all the results obtained at the time of presentation.

Jan 1, 1983

By J. J. Rush

Neutron scattering and analysis techniques are extremely powerful, often unique, probes for the characterization of the amount, location, bonding states, and dynamics of hydrogen in all classes of materials. Developments over the past decade at the NIST Center for Neutron Research and elsewhere have greatly increased the sensitivity and dynamic range of neutron methods. In this paper, we provide a flavor of the capabilities of modem neutron instrumentation for the study of hydrogen in a number of technologically interesting systems, including metal hydrides, fuel-cell materials, fullerenes, and disordered carbons.

Jan 1, 2002

By V. V. Geikhman

The paper updates the Plant experience in the development and implementation of an advanced environmentally friendly zinc production technology complying with the technological and economic level of producers in the world and the standards of maximum permissible gas emissions stipulated by the Russian legislation. General water recycling engineering allowed to ensure 95.6% water rotation level. All solid wastes formed during treating zinc concentrate are processed into marketable products or semiproducts and sold. As a result of implementing innovation techniques production at the Chelyabinsk Zinc Plant is non-waste.

Jan 1, 2006

By John L. Uhrie

Oxide stockpile leaching operations can realize increased copper recovery and decreased acid consumption from in-situ generated acid resulting from the oxidation of intentionally introduced pyrite recovered from mill tailings or other sources. While all oxide leach ores can benefit from pyrite addition, low acid consuming ores can show remarkably increased recovery and net acid generation; however, more highly acid consuming ores will show benefit more exclusively through increased copper recovery. Additional work shows that the value of highly acid consuming ores can be optimized by balancing copper recovery against acid consumption.

Jan 1, 1999

By Jorge Alberto Soares Tenório

Electronic components have precious metals like Au and Ag. These metals have a high performance in electric conductance. The recycling of the scrap, however is too difficult because of the presence of other metals like Fe, Al, Zn, Sn, ceramics and plastics, all together in electronic components. The aim of the present work was to define one way for physical separation to have metallic non-ferrous concentrates. It was used three kinds of scrap. I was used conventional equipment for mineral processing like hammer mill; screens, electrostatic and magnetic separation.

Jan 1, 1997

By Carlos Schvezov, Eliana Agaliotis, Alicia E. Ares, Mario Rosenberger

"The interaction between a solidification front and a spherical particle was modeled and simulated in order to study the phenomenon of ""pushing"". Finite element methods were employed in axisymetric domains. The drag force is calculated from the calculated fluid flow field and the repulsion force is the Lifshitz-Van der Waal force. The thermal field is decoupled from the force field. The model is applied to a metallic matrix containing particles with similar, lower or higher thermal conductivities than the matrix, resulting in planar, convex and concave interface shapes, respectively.The results show that the critical velocities for pushing for concave and convex interfaces are about one order of magnitude larger and one order of magnitude lower than the critical velocity for flat interfaces, respectively. The simulated results were in very good agreement with reported experimental results.IntroductionThe solidification interface of materials containing spherical particles in some cases can push the particle ahead the interface. This phenomenon generally occurs during the solidification of different materials such as, metallic alloys containing native particles, metal matrix composites containing particles or fibers as reinforcements and crystallization of semiconductor, optical, optoelectronic or biological materials. In all cases the interaction strongly determines the distribution of particles and the resulting physical and physic-chemical properties of the resulting material. The phenomenon has been investigated for many years both experimentally and by mathematical modeling [1-21]. The process is complex due to the variety of phenomena involved during pushing. In all cases, the physical problem depends on the properties, nature, and morphology of the interacting media; the particle, melt and solid; and external fields such as gravity, thermal and electromagnetic fields."

Jan 1, 2012

By Lan Li, Izaak Williamson

"The efficient separation and storage of CO2 from power plant flue gases can reduce the amount of CO2 released into the atmosphere and mitigate global warming. Potential candidates for industrial applications are solid sorbent materials. Crucial factors to control the efficiency of porous sorbent materials include the framework and pore structure, and the chemical and physical reactivity of CO2 within the pores. Computational modeling approaches, based on density functional theory (DFT) and van der Waals-DFT, have been applied to nanoporous solid – manganese dioxide a-MnO2. We found that the types and charges of cations as dopants in the a-MnO2 and the concentration of CO2 influence the structural features of a-MnO2, which control its CO2 selectivity performance within the flue gases.IntroductionCarbon capture and storage is a technique to separate large quantities of CO2 from power plant flue gases before being released into the atmosphere. Porous solids are a potential candidate as sorbents to “trap” CO2 through chemical or physical adsorption on their porous surfaces[1]. Such separation efficiency is determined by the size and shape of its pores and by the interaction between the porous surface and the gas adsorbates. The incorporation of cations into the pore can act as a means of structural support and alter the pore diameter to be comparable to the kinetic diameter of the gas adsorbate, such as CO2.A porous solid of particular interest for CCS is manganese dioxide a-MnO2, an octahedral molecular sieve (OMS) composed of edge-sharing MnO6 octahedra that are linked into a nanoporous framework[2]. The framework consists of (1×1) and (2×2) tunnels, referred to as OMS-2. Due to the larger tunnel size, cations and gas adsorbates prefer to reside along the (2×2) tunnel axis of the OMS-2. As seen in Figure 1, a potassium cation K+ is located in the (2×2) tunnel, known as cryptomelane-type MnO2. Its pore diameter of ~ 4.6 Å gives it a good CO2 selectivity performance, because the diameter is comparable to the kinetic diameter of 3.3 Å for CO2[3]. Alternatively, replacing potassium K+ with other cations, e.g. barium Ba2+, sodium Na+ or lithium Li+, in the OMS-2 tunnel is of great research interest, due to the effects of their concentrations, types and charges on the CO2 selectivity efficiency and sorption hysteresis phenomenon[2,4]."

Jan 1, 2014

By Thomas Buenger

The Hamburg smelter of Norddeutsche Affinerie AG is situated near the city of Hamburg’s downtown and is therefore particularly subjected to fulfill environmental requirements according to the German legal regulations. Thus, investments related to increasing concentrate throughput are always linked to packages to enhance the emission status of the smelter. This connection between environmental protection and productivity enhancement should be explained by the example of the Peirce-Smith converter plant of the Hamburg smelter. Such outstanding investments can be demonstrated by the transition from scrap charging via boat from the front side to a fully automatic and completely sucked scrap charging system.

Jan 1, 2009

By L. H. Lewis

The relationships that link microstructural properties of advanced permanent magnet materials with magnetic properties such as the coercivity are often difficult to quantify, especially in materials with nano-scale structures. Recent work on RE2Fe14B-based powders fabricated with rapid- solidification techniques such as inert gas atomization (IGA) and melt-spinning provide insight into the nanostructural features which affect the acquisition and stability of coercivity. In all cases the coercivity is found to be a function of both the scale of the constituent microstructure and of the presence and distribution of minor phases.

Jan 1, 1997

By Rolando Campos

The CODELCO-CHILE Teniente Converter Technology, is presently being applied in four Chilean smelters (Caletones, Chuquicamata, Potrerillos and ENAMI-Ventanas). A Teniente Converter is due to be used at ENAMI-Hernan Videla Lira (Paipote) smelter in the near future. Also, a Teniente Converter is to be installed as part of a retrofit project for Nkana smelter of Zambia Consolidated Copper Mines Ltd. (ZCCM). The charge to be treated through this smelter will consist of a blend of concentrate arisings from the various concentrators within the ZCCM group. The present status on the application of the Teniente Converter Technology at Caletones smelter as well as its projected performance when used at Nkana smelter, are presented in this paper. The design operational basis, autogenous smelting throughputs, concentrate to matte ratios and benefits due to the use of technical oxygen, are presented and analysed.

Jan 1, 1992

By M. D. Bishop

Loss of organic solvent extraction circuits occurs through several accepted methods. Losses are commonly attributed to entrainment of the plant organic and evaporative loss of diluent. Evaporative losses of diluent have been estimated using various models or by considering all losses over and above entrainment to be due to evaporation. Other possible loss mechanisms are discussed and data on losses during weather conditions are presented. Accurate estimation of evaporative loss is vitally important to the industry due to both cost factors and environmental concerns. Data for and description of the Diffusive Flux Model are presented as an improved-method of estimating evaporative losses:

Jan 1, 1999

By C. Dresen

This paper discussed the reaction kinetics of the reduction of industrial phosphate pellets for P4 production. In the reduction process of various phosphate ores, the following parameters were investigated: Diffusion of the phosphorus oxide and other gaseous products from the reaction mixture after having been reduced on the reductant (coke) surface. Influence of silica on reaction kinetics. Temperature influence. Influence of mineralogy and morphology (different ores). Particle size influence of silica and coke. Experiments were carried out in a vertical tube furnace with 2 ores, 2 types of silica and one type of coke. Selected experimental conditions simulated furnace conditions. The following conclusions could be made: Reaction rate increases with the addition of SiO2 into the pellet. The reaction rate increases above 1350°C (melting temperature of the slag). Mixing different ore types in the pellets leads to differences in reduction kinetics. Particle size of the coke particles influence reduction kinetics. The amount of slag formation is influenced by silica addition, coke size and temperature.

Jan 1, 2002

By Jin Zuomei

The kinetics of dissolution of nickel matte in the presence of manganese dioxide with silver ions was investigated. The catalytic silver ions enchanced the leaching rate up to a factor of 17. The effects of stirring, temperature, particle size, concentrations of Mn02, silver and ferric ions, and the experimental procedures were studied. Solid residues at various levels of nickel extraction were examined by SEM, TEM, electron micoprobe and X-ray diffraction. These results indicated that the dissolution reaction was topochemical and fits a surface reaction control model. The activation energy was calculated to be 39.15 KJ/mol. The leaching rate of Ni3S2 was independent with stirring rate, but the reaction rate constant was inversely proportional to the initial particle diameter. The order of the reaction rate are 0.41, 0.69, 0.33 with respect to Ag+, Mn4+ and Fe&apos;+ con-centration respectively. Thus a kinetic rate equation was developed. Moreover, we propose a mechanism of silver catalyzed leaching of Ni3S2&apos;

Jan 1, 1990

By Ehsan Vahidi, Fereshteh Rashchi, Amirhossein Shahnazi

"The pig iron from steel manufacturing plants contains a high concentration of vanadium-bearing materials smelted with iron ore. During the oxidation process of the molten pig iron with oxygen lances, vanadium transfers to the slag. In this research, recovery of vanadium from LD (Linz-Donawitz) converter slag of steelmaking plant was investigated. The leaching residue was characterized by XRD and XRF techniques. The maximum vanadium recovery was achieved at optimum leaching conditions of 70 °C, S/L: 1/15, sodium hydroxide concentration: 3 M and leaching time: 150 minutes. The dissolution rate increased with rising sodium hydroxide concentration and temperature and decreasing particle size. The experimental data are treated graphically to explain the kinetics of the vanadium recovery process using shrinking core model (SCM). As a result, the controlling regimes in the SCM were analyzed separately using liquid film diffusion control, solid product diffusion control, and reaction control mechanisms.IntroductionVanadium is commercially important as a constituent of several alloys and catalysts. Nowadays, vanadium is mostly recovered as a by-product from secondary sources or from industrial waste streams such as titaniferrous magnetite, fly ash, spent catalysts, and petroleum coke. Steelmaking operations are specifically concerned by this problem due to the production of a huge quantity of by-products [1]. These by-products, including LD converter slag, sludge, fly ash, spent catalyst, ash, and alloyed scrap, contain a notable amount of heavy metals which may cause environmental problems. Solvent extraction is one of the techniques being increasingly used for the recovery of vanadium [2]. Apart from vanadium ore, secondary resources such as titanmagnetite, ilmenite and slag from the ferrous industry are a major source of supply. The pig iron from steel manufacturing contains a majority of vanadium-bearing materials smelted with iron ore. In a heat resistant shaking ladle the molten pig iron is oxidized with oxygen lances, causing the vanadium to be transferred to the slag. Normally, the vanadium in LD converter steel slag (coming from Linz-Donawitz steelmaking process) is ca. 5% as vanadium pentoxide (V2O5). This slag is the world's principal raw material for vanadium production [3, 4]. Moskalyk and Alfantazi [4] reported that a roast-leach process is used in South Africa for the production of vanadium oxides from magnetite ores while some of the slag was converted to ferrovanadium. A portion of the slag was exported to Europe for the production of vanadium oxide. The researchers mentioned that alkaline roasting was the main process at that time employed to extract vanadium pentoxide from vanadium slags."

Jan 1, 2012