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By Akira Yazawa, Kazuo Koike, Mitsuhisa Hino

"The vapor pressures of MS (PbS, SnS and Sb2S3) in the molten Cu2S-MS, FeS-MS pseudo-binary and Cu2S-FeS-MS ternary systems were measured by means of a transportation method in the temperature range of 1323 and 1423K to calculate MS activities in the sulfide melts. The activities of MS in these systems show negative deviation from ideal behavior except the FeS binary systems which exhibit nearly ideal behavior in the homogeneous melts. The activities of the Cu2S-FeS pseudobinary system, which is fundamentals of the copper matte, were estimated from the activity values in the ternary systems and exhibit negative deviation from ideality.The distribution behavior of tin between the ·matte and silica saturated fayalite slag was investigated under the controlled partial pressures of S02 at l 523K. It was found that, in general, tin is distributed in the both phase, while tin is concentrated to the slag phase with increasing copper content in the matte. The activity coefficient of SnO in the slag was calculated based on the distribution ratio combined with the activity coefficient in the Cu2S-FeS system.IntroductionThe thermodynamic properties related to the Cu2S-FeS system and the Cu2S-FeS-MS systems (where MS can be PbS, SnS, Sb2S3, As2S3, Bi2S3, etc.) is required to be better understanding of the copper smelting process. However, thermodynamic analysis such as the distribution of impurities among the gas, slag and matte phases is difficult due to lack of thermodynamic data. In this study, the vapor pressures of MS (PbS, SnS and Sb2S3) in the Cu2S-MS, FeS-MS. and Cu2S-FeS-MS systems were measured by a transportation method. The distribution behavior of tin between the matte and silica saturated fayalite slag was also investigated. The results in the present experiments are useful to analyze thermodynamically the behavior of component in the copper matte smelting."

Jan 1, 2000

By Miaoyong Zhu, Sen Luo

"A two-dimensional CAFD model was developed for simulating the solute diffusion-controlled dentritic growth in the low Peclet number regime. Mass conservation and local equilibrium at the solid/liquid interface were solved to determine the growth velocity of interface with consideration of constitutional and curvature undercooling. The modified decentered square growth proposed by Wang et al was adopted to capture the first eight neighboring cells. The comparison between the classic Lipton-Glicksman-Kurz (LGK) analytical model for steady state tip variables and the simulated values showed that the present model was capable of quantitatively determining the dendritic growth, and the simulation tests demonstrated that the effects of the mesh anisotropy in growth kinetics and crystallographic orientation were eliminated. The numerical simulations were performed to the dendritic growth ofFe-0.6%C binary alloy in undercooled melt, and the results showed that the present model could predict the dendrite morphology with artificial growth orientation in acceptable level.IntroductionDuring the solidification of metals and alloys, the dendrite grows from the substance or the undercooling melt and solute redistributes between the dendrite and the interdendritic liquid. The solidification microstructure is close related to the phase and solute evenness and has a close linkage with the properties of final production.In the past few decades, various kinds of deterministic and stochastic models have been developed to predict the evolution of microstructures in solidification, with the fast development of computer power. Among these methods, Phase Field (PF) model [1, 2] has been known as one of the most adequate deterministic models for directly simulating the dendritic growth. However, there is a vital drawback that the PF method requires considerable computation time and is limited to simulate very small domains with a few dendrites [3]. On the other hand, stochastic models, such as Monte Carlo (MC) method [4, 5] and Cellular Automaton (CA) method [6-8], have been usually applied to predict the solidification microstructure evolution. Comparing with the MC method, the dendritic growth kinetics is explicitly integrated in the CA model, while the MC model doesn't. Therefore, the CA method is more reasonable to predict the dendritic growth during the solidification of melt."

Jan 1, 2013

By Gerardo Muñoz

All along this century CODELCO's smelters have been operating on conventional technology, which Codelco has streamlined by using oxygen, developing oxy-fuel burners for reverberatory furnaces and introducing oxygen smelting of concentrates in converters (Teniente Converters). Chuquicamata began capturing sulfur from its first Teniente Converter in 1985. Since then, it has implemented a program allowing to gradually increase such capture. In 1994 a Frame Law on the Environment was enacted in Chile. By virtue thereof and of CODELCO's corporate environmental policy, an investment program aimed at capturing more than 95% of gaseous pollutants in all its smelters in a term not exceeding twelve years was established. The above entails a substantial improvement of the operational management as regards fugitive gases capture and treatment. This paper describes the way CODELCO is to deal with this challenge with a view to fully complying with environmental regulations and obtaining the required environmental certifications of its operations.

Jan 1, 1996

By A. MacRae

Campaign life of the converting furnace has been limited by break-outs through the hearth and walls. Throughput of concentrate has increased by 60% since start-up of the copper operations in 1981. The Furnace Integrity program was initiated at Kidd in 1993 to improve the reliability and safety of the smelting-cleaning-converting furnace line. The converting furnace is undergoing a series of upgrades to overcome severe refractory wear to the roof, walls and hearth. A recent shut-down was held in March 1997 to implement improvements to the roof, walls and slag outlet. Wall modifications included a new upper shell, wall coolers which can be supported during a shut-down from outside of the vessel, and an increase in the number of cooling blocks. Improvements to the roof included increased cooling, a novel brick/cooler suspension system, and roof compression for gas tightness. Design is currently underway to deepen the refractory hearth, to decrease hearth erosion and increase resistance to flotation.

Jan 1, 1998

By Onuralp Yucel, Ahmet Turan, Halil Yildirim

"Nickel is mainly used in stainless steel production as ferronickel. In recent years, low grade ferronickel or nickel pig iron (NPI) is used in stainless steel production to reduce expenditure of nickel price. In this study, Turkey East Anatolian region lateritic nickel ores were directly introduced carbothermal reduction to produce NPI. Firstly the raw lateritic ore that contains 0.9% Ni, 0.054% Co and 2.3% Cr was mixed with metallurgical grade coal at different stiochometric ratios. The samples were smelted at 1600-1650 °C temperature range in an induction furnace for 25 min. In the second experimental set, different processes times were carried out from 15 to 35 min. The raw material, obtained alloys and slags were analyzed by using XRD (X-Ray Diffractometer), XRF (X-Ray Fluorescence Spectrometer), AAS (Atomic Absorption Spectrometer) and EPMA (Electron Probe Micro Analyzer) techniques.IntroductionNickel is an important element that has many application areas in the industry and there are a lot of kinds of nickel products such as refined metal, powder, sponge etc. 65% of metallic nickel is used in stainless steel, 12% is consumed as superalloy and non ferrous alloy because of its superior corrosion and high temperature properties [1].Nickel is a transition metal that is mined from mainly two types of ore deposits as sulphide ores and lateritic ores. Although 73% of nickel ores are laterites, 55% of primary production is from sulphide ores [1, 2]. The importance of lateritic ores is increasing due to the increase in nickel prices and decrease in reserves of sulphide ores.There are pyrometallurgical, hydrometallurgical and combined (pyro-hydrometallurgical) methods which are used for the extraction of nickel from lateritic ores. HPAL (High temperature pressure acid leaching) is generally used to recover nickel and cobalt from laterite nickel ores. It is suitable for the plants processing ores with low magnesium oxide and aluminum oxide content. Lateritic ores are exposed to hot acidic leaching around ~250 °C to dissolve cobalt and nickel under high pressure. The main disadvantage for HPAL is the high cost of titanium autoclaves. Process is complex and difficult to control due to the high pressure and heating of the process [2, 3 and 4]."

Jan 1, 2012

By Marcela C. Santini, Luiz A. Teixeira

"Surface conditioning (also referred as etching) of plastics prior to metallization is generally conducted with sulfuric I chromic acid solutions. Although these baths perform well technically, the presence of Cr (VI) imposes serious operating problems of an environmental nature. The present work reports ·the results of a study of surface conditioning o(ABS using solutions based. on sulfuric acid, with hydrogen peroxide and/or nitric acid, replacing chromic acid, as oxidants. Process performance was evaluated by SEM and by the uniformity and adherence of electroless nickel coatings applied on selected conditioned samples. The results showed that the evaluated types of solutions could be optimized to perform as well as the chromic-based baths, with a much superior environmental quality.IntroductionMetallization of plastics is normally undertaken for either decorative or functional purposes. Through metallization, the specific properties of plastics such as light weight, design flexibility, and low-cost of manufacturing are enhanced by the addition of properties usually associated with metals. These include reflectiveness, abrasion resistance, electrical conductivity, and a variety of decorative effects (1).The available processes that can be used for metallization of plastics are vacuum metallization or vapoµr deposition; indirect metallization and plating (1). Plating can be sub-divided into electroless plating and electroplating. In electroless plating, metal ions in aqueous solution are deposited on the .activated plastic surface by oxi-reduction reactions without the aid of an external electric potential, forming a thin metallic layer. This electroless deposited film has two functions: (a) it provides an electrically conductive substrate that allows further coating by electroplating; and (b) provides a secure bond between the plastic substrate and the electroplated layer (1,2). In case the electroless metallic part requires an additional layer for finishing purposes, or just an increase in thickness, the part can be additionally electroplated with a· variety of metals - in most cases those are copper, nickel or chromium (3)."

Jan 1, 2000

By R. N. O'Brien, E. Peters

"It has been discovered that copper concentrates can be leached in strong (40-60%) sulfuric acid with nitric acid, or with oxygen if nitric acid is present as a catalyst. Chalcopyrite is rapidly decomposed at temperatures well below the boiling temperature of the lixiviant (-150 C.) and the resulting copper and ferric salts are precipitated as CuS04.H20 and FeH(S04)z.4H20. Other metal sulfides such as zinc, lead, nickel, etc. are also converted to sulfates that are nearly insoluble. Sulfur is partially converted to elemental and partially to sulfuric acid. Reduction products of nitric acid can be recovered from the distillate with good recovery. Conversion of as-received copper concentrates is largely complete in about 1 hour. Introduction9 molar sulfuric acid is an unusual hydrometallurgical lixiviant: it has a boiling point of about 150 C. and a low solubility for base metal sulfates. Below about 6 molar acid, the boiling point falls below 120 C. and yields much higher sulfate salt solubility, while above 12 or 13 molar acid and at higher temperature sulfuric acid becomes an oxidizing agent, yielding gaseous S02' Thus, sulfuric acid within this range of concentration is capable of acting well above the temperature of boiling water without requiring autoclave conditions, and if typical oxidative leaching conditions are applied to suspended mineral sulfide concentrates, it is possible to obtain a conversion of these sulfides into 'crystalline sulfates. Thereafter, the sulfates can be separated by filtration or by solid - bowl centrifuge and the solution can be recirculated to the reactor vessel. Meanwhile, the solid sulfates can be treated in a typical hydrometallurgical circuit, i.e., dissolved in a return stream that is essentially water, separated from each other by, for example, solvent extraction, and recovered as metals by electrowinning."

Jan 1, 1997

By Ilona Johnson

United States metals and non-metallic minerals manufacturing consume about 5,000 trillion Btu annually. Various studies estimate that as much as 20 to 50 percent of this energy is lost as excess or waste heat. Recovery of waste heat can conserve energy, reduce operating costs, and lower environmental emissions. It would be valuable to quantify recoverable waste heat sources and identify the barriers that hinder its recovery. This paper provides an overview of waste heat losses specific to high temperature processes in primary metals and minerals manufacturing. It summarizes findings from a broader study conducted for the Department of Energy Industrial Technologies Program; the study evaluates energy losses, recovery practices and opportunities, and R & D needs for waste heat technology development.

Jan 1, 2008

By Mitsuru Tanahashi

Oxidation removal of boron from molten silicon by injecting oxygen and highly basic CaO-CaF2flux powder has been investigated with special attention to the dynamic behavior of the injected flux particles and gas bubbles. Since oxygen gas is injected into the melt, high oxygen partial pressure is maintained at the flux-O2-Si interface and the removal of boron proceeds under nonequilibrium conditions. By applying this process, boron concentration in metallurgical-grade silicon can be reduced to a single-ppm level. In this paper, the effects of the dynamic behavior of the flux particles injected into the silicon melt and the area of the reaction field (the flux-O2-Siinterface) formed in the vicinity of the flux-gas exit of the injection nozzle on the rate of the boron removal are discussed from the viewpoint of process dynamics. The experimental results clarified that the boron removal rate is affected by the kinetic energy of the flux particles which is determined by the injection conditions, such as the gas-flow rate of oxygen and the size of the flux particles. At higher oxygen gas-flow rates, the injected flux particles are expected to possess a significantly high kinetic energy such that they penetrate the O2-Si interface formed at the nozzle exit, which results in the formation of a new reaction field for boron removal. On the other hand, at lower gas-flow rates, the injected flux particles possess too low kinetic energy to penetrate the interface. In this case where the formation of the reaction field is limited, it is shown experimentally that the rate of the boron removal is constant, independently of the flux injection rate.

Jan 1, 2006

By Jae-Chun Lee

Di-2-ethylhexyl phosphoric acid (D2EHPA) is widely used for separating rare-earth elements. In commercial plants, rare-earths are usually stripped from loaded extractant streams using mineral acid, then precipitated as oxalates. Many rare-earth uses demand specific powder characteristics, which are obtained by secondary processing. This paper demonstrates the feasibility of combining the stripping, precipitation and powder processing stages, thereby achieving considerable savings. MEHPA solutions were loaded with yttrium, then emulsified with oxalic acid-HC1 solutions to precipitate yttrium oxalate, which was readily calcined to yttrium oxide. The precipitation kinetics and yield were sensitive to process conditions. The morphology and size of the yttrium oxalate powders varied with the concentrations of D2EHPA and oxalic acid, and the presence of SPAN 60, which affected nucleation, growth, and the emulsion characteristics.

Jan 1, 1992

By P. K. Jimack, C. E. Goodyer, A. M. Mullis, P. C. Bollada

"We review the application of advanced numerical techniques such as adaptive mesh refmement, implicit time-stepping, multigrid solvers and massively parallel implementations as a route to obtaining solutions to the 3-dimensional phase-field problem with a domain size and interface resolution previously possible only in 2-dimensions. Using such techniques it is shown that such models are tractable even as the interface width approaches the solute capillary length.IntroductionMulti-scale modelling impinges upon many areas of science, engineering and technology where the interplay between processes occurring on disparate length and/or timescales can affect the properties of systems in a complex, and sometimes unforeseen, manner. One such is the processing of materials where interactions at the atomic scale, through the nano- and microstructural scale can have a profound affect on the macro-scale response of engineering components. Here we focus on one such problem, the crystallisation of alloy melts, to illustrate how a range of advanced numerical techniques make the modelling of such systems tractable.The modelling of solidification structures, in particular the growth of dendritic crystals, is a subject of intense and enduring interest within the scientific community, both because dendrites are a prime example of spontaneous pattern formation and they have a pervasive influence on the engineering properties of metals. For alloy systems, which form the vast majority of engineering materials, solidification involves the rejection of both solute and latent heat from the growing solid, forming a coupled diffusion problem in which both the chemical and thermal diffusion equations should be solved. The multi-scale nature of this problem arises from the disparity between the thermal and solutal diffusivities for most liquid metals, which are typically 10-5 m2 s-1 and 10-9 m2 s-1 respectively. The ratio of these two, referred to as the Lewis number (Le =Dia), is therefore typically of the order 10,000 and gives a measure of the multi-scale nature of the problem. In fact, in many cases the thermal diffusivity is so much larger than its solutal counterpart that thermal diffusion is considered instantaneous, wherein the system can be approximated as isothermal such that the multi-scale calculation does not need to be performed. This is certainly a reasonable approach in most conventional castings. However, there is a class of solidification problem in which this approach is far from satisfactory, namely Rapid Solidification (RS). The application of isothermal phase-field models in such situations are highly likely to produce spurious results or to fail totally, particularly for temperatures below To (the temperature at which the free energies of the solid and liquid phases are equal at the concentration of the bulk alloy), wherein partitionless solidification may occur."

Jan 1, 2013

By Maneesh Singh

During the various stages of iron & steel production a number of iron-rich by-products are generated. The traditional way to recycle them back to the blast furnace has been the balling - sintering process. These by-products can also be made into cement-bonded agglomerates for use as burden material for blast furnaces. In order to improve the quality of agglomerates the effects of various processing parameters on the properties of cement-bonded briquettes have to be controlled. This paper looks into the various aspects of producing cement-bonded agglomerates and using them as burden material for blast furnaces.

Jan 1, 2003

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 Catherine Williams-Beam

Thallium is more toxic to humans than mercury, cadmium, lead, copper or zinc. Its chemical behavior resembles the alkali metals (K, Rb, Cs). It occurs almost exclusively in natural waters the monovalent thallous cation. The solubilities of thallous compounds are relatively high so that monovalent thallium is readily transported through aqueous routes into the environment. The major sources of thallium are the base metal sulfides and precious metal bearing sulfides. Therefore, it is often present as a contaminant constituent in waters emanating from heavy metal sulfide bearing deposits. Thallium can be effectively removed from wastewater to <2 µg/L by reductive precipitation of thallium sulfide. Effective thallium sulfide precipitation requires a controlled solution potential/pH combination. The required potential can be effectively achieved by utilizing a particulate iron slurry or packed column environment. Experimental results will be presented and discussed.

Jan 1, 2003

By R. G. Reddy

The oxidation kinetics of A13Ti intermetallics have been studied at the temperature range of 850°C to 100O0C in pure dry oxygen. The oxygen diffusion rates were investigated using TGA method. Parabolic rate constants were calculated. The oxidation scales were analyzed using SEM, EDS and X-ray diffraction. A continuous A120, scales with a little TiO2(rutile) were formed on the intermetallic surface. The A13Ti intermetallic exhibited excellent oxidation resistance among the Ti-Al base intermetallics.

Jan 1, 1997

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 Alireza Zakeri

To evaluate the behavior of minor elements in the copper smelting process, activities of silver, selenium and tellurium at minor concentration were determined at 1473 K within the miscibility gap of the Cu-S-Me (Me = Ag, Se, Te) and Cu-Fe-S-Me systems varied in Fe/Cu ratio. Phase relations between the immiscible metal and matte phases in the foregoing systems were first established by a quenching technique at 1473 K to supplement the activity measurement data. A Knudsen-effusion mass spectrometer, capable of handling complex gaseous systems and relatively small vapor pressures, was adopted for activity determination. Using a multiple Knudsen-cell, the ion intensity of minor element in the sample under study was measured simultaneously with that in a reference sample. Activity was obtained from the ratio between the measured ion intensities as well as the known activity value of the minor element in the reference sample. Limiting activity coefficients of the minor elements were correlated with composition of the matte. Based on the experimental results, the vaporization behavior of the minor elements has been discussed.

Jan 1, 1999

By Alex Probst

With low metal prices and increasing value placed on plant water and tailings disposal areas, it is becoming essential to maximize the efficiency of solid-liquid separation processes. Since its inception over 25 years ago, the use of flocculants has grown exponentially. While flocculants play a crucial role in the sedimentation process, they are also a major operating cost. Recent innovations are revolutionizing the industry once again. New thickener designs are doubling thickener-loading rates while reducing flocculant consumption. The feedwell, as the heart of the thickener, is undergoing many significant metamorphoses. With CFD and other advanced computational analysis, feedwell technology is being examined more thoroughly than ever before, The result is that the thickener previously thought of, as a "Black Box" is now being mapped and controlled with state-of-the-art technology. This paper will examine recent design improvements in all aspects of thickeners in order to project the look of the thickener of tomorrow.

Jan 1, 1999

By N. Verbaan, E. Bourricaudy, M. Dry

"Starfield Resources is developing a novel circuit for the recovery of nickel, copper, cobalt, iron oxide, sulphuric acid and precious metals from the Ferguson Lake deposit in Nunavut, Canada. In this deposit, pentlandite is too finely disseminated in pyrrhotite for the production of a smelter-grade nickel concentrate at an acceptable nickel recovery, so established technology is not applicable and a novel chloride-based circuit is under development. The enabling aspect of this circuit is the hydrolysis of ferric chloride to hematite, releasing gaseous hydrochloric acid that is recycled. Conventional steps are used for separating and recovering the valuable metals from the chloride solution generated. This paper briefly outlines the circuit and presents the results of experimental work on the enabling steps, viz. the oxidation and hydrolysis of iron chloride to hematite and gaseous hydrochloric acid.IntroductionThe Ferguson Lake bulk sulphide ore body in Nunavut, Canada, owned by Starfield Resources Inc., contains significant amounts of base and precious metals but its mineralogy is such that it is not amenable to conventional processing. Pentlandite, for example, is too finely disseminated in pyrhhotite for even modem techniques such as fine grinding and improved flotation reagents to be effective [ 1] and extracting the value requires processing the entire bulk sulphide, including the pyrrhotite. To give the project a total green footprint, in terms of both carbon emissions and acid rock drainage, Starfield imposed the following requirements:• No reactive tailings to generate acid rock drainage.• No gaseous emissions other than normal atmospheric constituents.• No liquid effluents.• No regular consumption of fossil fuel.• High recoveries of all the valuable metals."

Jan 1, 2011

By U B. Pal

Downsizing and decommissioning of nuclear facility operations is increasing the stockpile of various different grades of Radioactive Scrap Iron (RSI). Disposal of this material not only represents significant resource and value lost, but also necessitates long term monitoring for environmental compliance. The latter results in additional recurring expense. It is desirable to be able to decontaminate the RSI to a very low level that can be recycled or used for fabrication of containers for RSI disposal instead of using virgin metal to fabricate the container. Electro-Slag Remelting and Refining (ESR) is often used for decontaminating radioactive contaminated sources of scrap iron such as stainless steel. Non-radioactive oxides of cerium are used to simulate the radioactive oxide contaminants of Uranium and Plutonium. The success of the ESR process is strongly dependent on the capacity of the slag to rapidly incorporate the radioactive contaminant (simulant). In this study we have measured the slag-metal partition coefficient for cerium and investigated the reaction mechanism for the dissolution CeO, in the slag.

Jan 1, 2002