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By Akira Yazawa

The continuous converting has attractive advantages, but further experimental studies on the slag are required, when the process is considered thermodynamically. The summarized experimental results, obtained with iron silicate slag and with ferrite slag and results relating to actual operation are described and discussed in this paper. At first, equilibrium relations at controlled oxygen potentials among three melts of silica-saturated iron silicate slag, white metal and copper are investigated. The results obtained for slag agreed with the thermo-dynamical predictions. Namely, to suppress a magnetite separation, the system should be at high temperature; in the case of the S02 gas of 10 kPa, for example, magnetite did not separate from the slag at 1300°C, but at 1250 and 1200°C the slag was saturated with magnetite even at lower SO2 pressure. Copper losses caused by dissolution of its oxide increased with increasing 5O2 pressure, and were slightly lower than those reported in previous papers without the matte phase. When the continuous converting slag does not contain any appreciable amount of silica - in contrast to the conventional smelting slag ferrite slag would form, but there was no published fundamental work on-ferrite slags. Hence, the melting behavior and activities of the system CaO-Cu2O-Fe2O3 have been investigated. The liquidus diagram in nitrogen atmosphere was, constructed using both thermal analysis and quenching method. The low liquidus temperature region without magnetite separation was found in the part of low content of Cu2O in the section Cu2O-CaO-Fe2O3 and Cu2O?Fe2O3¬CaO?Fe2O3. The activity of Cu2O in the system was also measured. Slags, composed-of CaO, Cu2O and Fe2O3, in platinum crucibles were equilibrated at 1250°C and controlled oxygen pressures. After quenching, the-composition of slag and platinum crucible were determined qualitatively. On the thermo-dynamic analysis of the results, iso-activity lines were drawn, and it was shown that the slag in the converting furnace of the Mitsubishi process exists in an adequate region of the composition triangle.

Jan 1, 1976

By P. N. Anyalebechi

Keywords: Aluminum alloy 3004, Solidification rate, Homogenization, Second phase particles The effects of the fineness of as-solidified cast microstructure and temperature on the response of aluminum alloy 3004 to homogenization heat treatment (a.k.a. preheat) have been investigated. The study was conducted at 538oC and 595oC on directionally solidified laboratory-size ingots with a range of solidification rate of 0.10oC/s to 29.4oC/s. Optical and electron microscopy, quantitative image analysis, electrical conductivity, and electron probe microanalysis were used to quantify the effects of the homogenization heat treatment on the microstructure of aluminum alloy 3004. In general, increase in fineness of as-cast microstructure and homogenization temperature enhances the a-transformation reaction, dissolution of Mg2Si, elimination of dendritic microsegregation, and dispersoid formation. The homogenization heat treatment reduces the average size of second phase particles in castings solidified at <1oC/s. However, in castings solidified at above 1oC /s, homogenization causes the coarsening of the second phase particles. Mn in solid solution is independent of homogenization heat treatment temperature.

Jan 1, 2005

By Chris Doyle

From 1997-2000. PT INCO undertook the Fourth Line Expansion Project (FLEX) to increase annual production rates from 90-100 to 150 Mlbs Ni/year (68,000 MT Ni/yr). In 2003, PT INCO nickel production underwent a major sustainable step jump that finally exceeded the targeted rate. This paper presents the changes that led to this achievement. The focus of mining changed. Improving Ni grade was important but only if electric furnace feed met target chemistry so that on-specification slag could be produced. The intensity of diamond core drilling for exploration was dramatically upgraded, mine planning strategy was totally re- vamped and an ore chemistry quality assurance team was formed. In the processing plant, measurement systems were upgraded for better control. Teamwork between sections vastly improved. The final step jump in production occurred when the fifth hydro-electric power generator was added to the furnace grid to allow the power-starved furnaces to cruise in operation at 70+ MW. Keywords: Free cash flow, Ore Chemistry, Measure, Control, Improve

Jan 1, 2004

By Ruiqing Li

It is possible to purify some liquid metals by exploiting the difference between the vapour pressure of the bulk metal and the minor constituents or impurities. The rates of purification can be improved by carrying out the process under reduced pressure, that is, so called, vacuum. Some commercial examples of vacuum refining are the purification of molten tin to eliminate trace amounts of lead and the refining of cobalt, also to remove lead. The objective of this paper is to review the basic theory behind vacuum refining technology in order to show how the feasibility of vacuum refining can be determined simply for a particular system by evaluating Olette&apos;s Volatility Refining Criteriont.

Jan 1, 1991

By Peter G. Smith

Tri-calcium aluminate (TCA) is a dominant alkaline component of the red mud residue from the Bayer process. A method being considered for industrial implementation partially neutralizes the residue by contacting it with gaseous CO2. This paper outlines the chemistry of CO2neutralisation of TCA under conditions relevant to the treatment of Bayer residue. CO2 neutralisation of the liquor is fast. It results in the formation of amorphous aluminium hydroxide and dawsonite that agglomerate together. Neutralisation of solid TCA is slower and leads to the formation of calcite, dawsonite and amorphous aluminium hydroxide. The dissolution of TCA in partially neutralised slurries causes pH reversion. However the carbonated solutions contain a store of bicarbonate that can supply aqueous carbon dioxide to complete the transformation. The pH at which the carbonation is carried out will affect the degree of TCA transformation during the carbonation process. In particular, if the pH of the carbonation is too low (near 7.0), calcite precipitation is inhibited and the degree of transformation is low. Controlling the carbonation pH helps to optimise the neutralisation process.

Jan 1, 2003

By Chikabumi Yamauchi

The comprehensive scientific development of conventional industrial technologies stimulates the creation of new ones in the next generation. Prof. Akira Yazawa has just accomplished such an important work in the non-ferrous pyrometallurgical field. The results of his successful research are immortal. The research group of the author has conducted since 1985 fundamental studies on the application of sodium carbonate slag to copper fire refining. In the present paper, a calculation method for the distribution ratios of impurity elements between sodium carbonate slag and molten copper will be shown. The specific treatment by sodium carbonate slag will also be presented as an effective way for reducing each impurity content in the molten copper to 0.1 mass ppm, which is the level required for the production of high purity copper. The thinking-out of this evaluation method gets a hint from the Equation (2) in the text which was proposed by Prof. Akira Yazawa.

Jan 1, 2003

By Lloyd R. Nelson

Selective carbothermic reduction is the preferred method of treatment of electric arc furnace (EAF) dust (listed hazardous waste, K061). The process maximizes the recovery of recyclable constituents by concurrent production of saleable zinc metal (directly condensed from the furnace off-gases), an innocuous, disposable iron oxide-rich slag, and some metallic iron. Results of a mineralogical investigation of a foaming slag produced during selective carbothermic reduction treatment of EAF dusts are presented. Wiistite and tricalcium silicate were identified by reflected light microscopy as the primary crystalline phases contained in a glassy matrix, but this technique failed to reveal any solid phases that could have significantly contributed to foam stability. It was concluded therefore, that the foam had been unstable, and had been primarily generated by copious gas evolution associated with the sudden reduction of the slag by an inadvertent addition of carbonaceous reductant. This is consistent with the susceptibility to foaming, when subjected to sudden excesses of carbon, of the slags produced by selective carbothermic reduction, because they still contain unreduced components such as iron oxide.

Jan 1, 1994

By A. V. Tarasov

Regeneration of carbide waste from hard-alloy (sintered carbide) manufacture is an important scientific and technical objective aimed at improving the degree of recycling of rare metals (W, Co, Ta, Ti, Nb). Currently, the degree of recycling of those metals does not exceed 25% to 35% of their total production even in industrially developed countries. This is attributed to a significant extent to the substantial drawbacks of the technologies applied for their processing (environmental pollution, limitations to the use of regenerated products for important applications, sophisticated equipment to be used). An innovative environmentally sound technology has been developed in the Institute of Metallurgy of the Russian Academy of Sciences (IMET RAN) for processing of carbide waste of WC, TiC, TTC and other carbides using asymmetric alternating current of industrial frequency (the electrolyte used for this purpose is nitric acid solution). The current efficiency under optimal conditions is as high as 96% to 98%. The process has been tested on bench scale. The following commercial-grade products are obtained: pure ammonium paratungstate, tungstic acid, cobalt oxide, titanium dioxide and tantalum-niobium concentrate. The total metals recovery is 98% to 99%.

Jan 1, 2006

By M. Cross

Heap leaching presents a complex physico-chemical process to model and a significant challenge to develop a comprehensive model enabling reliable predictions of heap behavior over the long term. A computational modeling framework is described for the analysis of multi-phase flows in reactive porous media suitable for tracking metals recovery, for example, in heap leaching and environmental recovery processes. This modeling framework employs appropriately formulated, parameterized, and solution procedures to capture: 1) liquid and gas flow through heterogeneous porous media subject to variably saturated flow conditions, 2) the complex and dynamically changing nature of the porous media structure, 3) the transport of reactants and products of reaction, 4) the simultaneous mass and heat transfer, and 5) the role of bacteria as a catalyst for reactions. A second class of challenges to accurately model heap processes is to identify and then capture all the process data to characterize the reactivity of particular ores, the mine planning for the construction of the heap, leach schedules, meteorological data, etc. The objective of this paper is to outline these challenges and to describe a modeling framework that can cope with arbitrarily complex geometries and provide tools for rapid and accurate process assessment.

Jan 1, 2006

At the present time, cyanide is the most widely used reagent to extract gold from its ores and concentrates. However, its use in mining has become the focus of intense attack by various groups throughout the world; as a consequence, a renewed effort has been launched to find suitable alternative lixiviants to recover gold. Chlorination was the most popular process to extract gold, before it was rendered obsolete with the advent of the cyanidation process at the turn of the last century, not least because it required the use of potentially hazardous and costly chlorine to oxidize/complex the gold. The PLASTOL® process, originally designed to recover the platinum group metals (PGM?s) from their ores and concentrates, provides an alternative to cyanide for gold ores. The process generates oxidizing conditions in the autoclave capable of forming the AuIII ion, and gold chloro-complexes result from the addition of small quantities (~5-10 g/L) of sodium chloride to the autoclave. The principles of the PLASTOL® process are briefly described, and several applications of the process to gold concentrates are presented. Various options available to recover gold from PLASTOL® leach solutions are also discussed.

Jan 1, 2003

By Othon do Rêgo Monteiro Neto

[The present study has investigated the extraction of copper from a chalcopyrite flotation concentrate using an adapted strain of Thiobacillus ferrooxidans and shake flasks, tank leaching and Warburg respirometer techniques. From the shake flask experiments, the activation energy and the frequency factor have been determined to be ?ka = 59.4 kJ and A = 3.3 x 105 S-1, respectively. The temperature coefficient was found to be Q10 = 2.2 in the range of 20 to 35°C. It was suggested that the reaction mechanism of chalcopyrite leaching by T. ferrooxidans involves the formation of an activated complex. whose thermodynamic values have been calculated to be ?G? = 92.1 kJ, ?S? -148.8 J K-1 and ?H$ = 47.8 kJ. The maximum volumetric oxygen mass transfer coefficient for the reactor leaching was found to be achieved by using an optimum air flow rate of 1970 cm min l at a rotational frequency of 1000 min-1. The highest copper extraction in tank (reactor) leaching experiment was 86.8% after 17 days of leaching, while in the sterile runs the corresponding copper extraction was only 40.1%. The copper extraction was suggested to be diffusion controlled. The power requirement of the aerated reactor was calculated to be Pg = 2.02 watts. During leaching, the oxygen saturation concentration was found to be C* = 6.70 mg dm-3. Using the gassing out method the critical oxygen concentration was assessed to be CCrit 0.05 mg dm 3. From the Warburg experiments, the kinetic parameters of the Monad equation were derived with a new evaluation technique to be Vmsp = 9.0 µm3 02 min-1 mg protein-1 and K = 7.4% pulp density for the effect of substrate concentration. The order of reaction and the overall reaction rate constant were determined from the modified van&apos;t Hoff plot to be n = 0.0 and k = 1.49 p dm3 02 min-1 mg Protein -1 for the chalcopyrite concentrate oxidation by T. ferrooxidans. On the basis of this experimental work, a preliminary flow sheet has been proposed for the bioextraction of copper from flotation concentrates.]

Jan 1, 1985

By T. Inami

The chlorine leach of the anode slime was studied in order to improve the treatment process at the Niihama Nickel Refinery. The anode slime originates from the nickel matte electrorefining and, contains 3-5% of nickel as sulfides. A comparative study has been conducted on the filter cake resulting from the sulfur filtration of the molten anode slime. The kinetic factors of the chlorine leach such as temperature, grain size were defined. Under the optimized condition, 70-80% of the nickel is recovered from the slime or filter cake. On the basis of these results, the chlorine leach process for the treatment of anode slime has been established. The leaching plant has been installed and successfully operated since 1986.

Jan 1, 1988

By J. Phillip Mackey

The Peter Hayes Symposium on Pyrometallurgy, held as part of Extraction 2018, is an acknowledgement of his contributions to the basic science and principles underpinning modern pyrometallurgical processing. After completing his PhD at Strathclyde University, Scotland, in 1974, Peter took up a teaching position at The University of Queensland, Brisbane, Queensland, Australia in 1976. Peter Hayes’ research at the University since then has been focussed on: • The mechanisms and kinetics of heterogeneous solid/solid, gas/solid and liquid/ solid reactions, and • Experimental measurement of phase equilibria in complex high temperature metallurgical systems. This paper provides a brief biography of Dr. Peter Hayes and gives a full listing of Peter Hayes’ publications.

The entrainment of copper matte in the slag during the slag skimming stage of a Peirce-Smith converter was studied with a dam break model. Experiments were carried out with a range of fluid pairs where the lighter fluid was allowed to overflow a weir and the amount of entrained heavier fluid measured. The resulting entrainment is measured as the ratio of the heavy to light fluid withdrawn. The fluids include oil-water, water- glycerol and salt solutions-water pairs to cover a wide range of densities and viscosities. It was found that the Richardson number, Ri, correlates the entrainment well. For the case of the liquid-liquid interface initially at the same height as the weir, the entrainment was found to vary with Ri-1/3. The transient flow was simulated with a volume of fluid (VOF) code written in-house and used a stairstep approach to represent flow obstacles. The code was validated against the experimental results with good agreement for the variation of the heights of the two fluid with time. The simulation showed that the prevailing mechanism for entrainment is due to a pressure differential created across the liquid in the converter during pouring resulting in the heavier liquid being rotated upwards and over the weir.

Jan 1, 1999

By V. A. Bryukvin

It has been found that by superimposing symmetric alternating current over the process, the rate of nickel and cobalt leaching from metallized products with copper sulfate solutions increases by a factor of 1.5 to 2.0 and the apparent activation energy of the process investigated is reduced from 12 down to 6.6 kcal/mole. It appears especially attractive to use alternating current for anodic dissolution (oxidation) of metallic scrap of refractory metals and their alloys in ammonia electrolytes permits production of high-grade commercial products in the form of respective ammonium salts using a short and virtually reagent-free process flowsheet. Similar approaches can be applied also for electrochemical processing of nickel and copper scrap in sulfuric acid media with subsequent recovery of pure sulfate salts or electrolytic processing. Electrochemical technology for recycling of tungsten-cobalt (WC 15) and tungsten-rhenium (WR 20) alloys has been also investigated. In the former case, anodic oxidation of carbide alloy was carried out in nitric acid electrolyte with production of pure tungstic acid. The research conducted has indicated that the physicochemical effect of alternating current results in a lower activation energy of electrode reactions due to changes in the mechanisms of the electrode reactions themselves.

Jan 1, 2006

By Guy Deschênes

In spite of the wide use of lead compounds to enhance cyanidation of free milling sulphide-bearing gold ores, an industrial control method was only implemented four years ago. This study presents the results of the investigation that led to the development of the on-line control technology. Two free milling sulphide-bearing gold ores and high purity minerals were used to develop and test the concept. The first ore contains 2.8 g/t Au, 6.2% pyrrhotite, 2.1% pyrite 0.6 % arsenopyrite, 0.1% chalcopyrite and 0.1% organic carbon. The second ore contains 10.4 g/t Au, 3.2% pyrite, 0.8% pyrrhotite and 0.38% chalcopyrite. The first ore showed a much higher oxidation rate in the pre-leach than the second one and consumed seven times more cyanide. A relation between the formation of thiosulphate and thiocyanate and the additions of lead nitrate were quantified. The ?reducing power?, a titration with permanganate, predominantly determines the concentration of thiosulphate and thiocyanate in cyanide solution. The relation between the reducing power and the addition of lead nitrate at various concentrations of pyrrhotite and chalcopyrite in the ores was established, providing a monitor/control strategy for lead nitrate addition.

Jan 1, 2006

By Marco A. S. Aguiar, Luis G. S. Sobral, Vânia Mori, Paulo A. Medeiros da Silva

"Copper occurs in the crust of the earth, predominantly, as sulphides. Among the copper sulphide minerals, the chalcopyrite is the most abundant and the most refractory to the conventional oxidative processes. This work aims at developing an electrolytic process for treating a copper sulphides flotation concentrate, more precisely chalcopyrite (CuFeS2) and bornite (Cu5FeS4) in the percentages of 70 and 30%, respectively.This paper presents a low-cost operational electroleaching process for treating copper sulphides flotation concentrates, with a high chalcopyrite content. This research practical work aims at improving the copper extraction from that sulphide mineral, in a relatively short time with low-operating cost taking into consideration the influence of a cationic surfactant. The electrolyte of the electrolytic reaction system was a 2,0 mol.L-1 NaCl solution containing CTAB, a cationic surfactant. The electroleaching system contains one DSATM (dimensionally stable anode) anode and two nickel or copper foams (threedimension electrodes. During the electroleaching process the chloride ions are oxidized to chlorine at the anode surface, which in contact with the aqueous phase generate enough hypochlorite ions to oxidize chalcopyrite.The copper ions released from the chemical oxidation process are reduced at the cathode surface as metallic copper."

Jan 1, 2008

By Norihiro Murayama

The hydrothermal syntheses of zeolites from coal fly ash were carried out using NaOH and KOH as an alkali source. The cation exchange capacity (CEC) and the ion exchange selectivity were investigated for the zeolites synthesized by a hydrothermal treatment. The effective usage of the zeolite as a cation exchanger was considered from the viewpoint of engineering. Zeolite P, HS (hydroxysodalite) and K-CHA (potassium-chabazite) are mainly formed as zeolite species in NaOH or KOH solution at 393K. The zeolite P and K-CHA have a large exchange capacity as a cation exchanger. The cation exchange isotherms of various monovalent and divalent cations with various zeolites are investigated. The order of selectivity of the zeolites is as follows, NH4+> K+> Li+.For the divalent cation, the largest removal amount is obtained for Pb2+ in the low equilibrium concentrations below 0.2mmol/dm3, and almost perfect removal can be achieved for Pd2+. The order of selectivity of zeolites in low concentration is expressed in the following order; Pb2+> Co2+> Cd2+> Ca2+> Mg2+> Ni2+. Ii is considered the zeolites obtained from coal fly ash can be used as an excellent cation exchanger.

Jan 1, 2006

By E. M. Timoshenko

Autoclave technology can be effectively used for liberation of complex mineral raw materials to transfer valuable constituents into solution for their subsequent recovery or to refine feed material in order to remove deleterious impurities, e.g. arsenic. The high efficiency of autoclave processes is attributed to the fact that they are suitable for processing of refractory raw materials, have low capital costs, high productivity, ensure integrated utilization of the feed materials, produce innovative saleable products, completely eliminate any air emissions, provide low-waste or waste-less technology, mechanization and automation of production processes. In the immediate future, it might be expected that autoclave processes will find use on commercial scale for production of heavy non-ferrous metals in combination with other processes (hydrometallurgical, upgrading, sorption and solvent extraction, electrolytic, etc.) to ensure: - Integrated processing of refractory ores and concentrates (pyrrhotite, zinc, copper-zinc, lead-zinc, nickel-cobalt, copper, pyrite); - Production of metallic powders of base metals as commercial products (copper, cobalt, nickel, etc.), composites on their bases, final products and saleable salts. Processing technologies incorporating autoclave processes, especially at the stage of liberation (chemical upgrading) of raw materials are characterized generally by high overall recoveries of valuable constituents significantly exceeding recoveries common for conventional pyrometallurgical processes (for some elements by several tens of percent).

Jan 1, 2006

By H. Y. Cheng

A pulse column solvent extraction system was evaluated as an alternative to mixer-settlers for the separation and purification of rare earths. The column tested had an inside diameter of 44.5 mm and had 36 sieve plates with a free area of 25%. Pulsing was provided pneumatically using a solenoid valve controlled by a timer so that both pulse amplitude and frequency could be varied. Feed to the column was a mixed rare earth chloride solution containing 10 g RE L-1. The extractant was 5% Ionquest® 801 in Shellsol 2037 diluent. Hydraulic performance of the pulse column was excellent with no propensity towards stable emulsions or crud formation under normal operating conditions. The column was operated in organic-continuous mode with flow rates chosen so that yttrium and the heavy rare earths were extracted with high efficiency while the light rare earths were rejected. Yttrium extraction varied from 83 to 99.2%. Concentration profiles were measured in both the aqueous and organic phases, and, from this data, the height of a transfer unit (HTU), the mass transfer coefficient (Kxa) and the continuous-phase axial dispersion coefficient (Ey) were computed. The HTU ranged from 17-92 an which is within the range of values reported for other (non rare earth) pulse column systems.

Jan 1, 1992