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By Khosrow Nikkhah

Increasingly ion exchange systems are being included in design of hydrometallurgical plants for metal extraction or impurity removal. Because such systems operate sequentially and are based on resins that exchange one ion for another, store it temporarily and release it to a regenerating solution, the usual steady state heat and mass balancing tools and spreadsheets cannot be used to design them successfully. This paper outlines the role of dynamic simulation in design of ion exchange systems. Examples are given for use of dynamic simulation in design and investigation of equipment based on consideration of the effect of input criteria such as expected ion loading and elution profiles. The methodology for dynamic modeling using IDEAS in design of multi column ion exchange trains operating in parallel is presented. Results shown include the non-steady state distribution of extracted metal and limitations imposed on operating conditions. These conditions include proposed sequencing of columns for loading and elution cycles, loading, elution and recycle flow rates as well as size and choice of related ion exchange plant equipment.

Jan 1, 2003

By Qingcai Liu

The effect of the TiC addition on corrosion resistance of the Al2O3-C refractories in smelting reduction melts has been studied by quasi-station immersion and rotary immersion. The corrosion rate of Al2O3-C refractories is decreased with the TiC addition. The corrosion mechanism of Al2O3-C refractories is oxidization of graphite carbon by the oxides of the melts and the formation of deteriorate layer.

Jan 1, 2006

By Katragadda Sarveswara Rao

"In view of the increasing importance of processing lean ores as potential future resources, efforts are being made worldwide to develop suitable technologies for the recovery of both nonferrous, base and precious metals. There are various types of low grade ores present in many countries. Gradually, the mineral reserves for production of metals have undergone complex changes with regards to their grades and particularly the physical and chemical properties of the minerals to be separated from each other. So, there is a need for new processing routes or the upgrading of existing technologies to recover metal values that are otherwise unutilized. Accordingly, an overview of the different types of mineral resources and economical processes, based on ore horizons, consumption of energy and reagents and environmental concerns, is made in this paper. In addition, the paper provides a summary of metallurgical and engineering challenges to be overcome when implementing new technologies and concepts with regard to base metal extraction and sulphur removal efficiency.IntroductionLow grade multimetal complex sulfide ores are likely to become an importance source for nonferrous as well as precious metals in the near future. The principle metallic minerals are chalcopyrite, sphalerite, galena, pyrite, pyrrhotite, arsenopyrite, tetrahedrite, boulangerite and cassiterite. Such ores are located throughout the world as multi-pocketed reserves which have present complex challenges with regard to their grades and particularly the physical and chemical properties of the minerals to be separated from each other. Their compositions can vary widely from one deposit to another and even from one location to another in the same deposit, and this poses a problem for the recovering metals present therein. Successful aqueous processing of complex sulphide ores depends on the composition and mineralogy of the raw materials and on their leaching behaviour."

Jan 1, 2012

By Daniel Kim, Justin McAllister, Shijie Wang

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

Jan 1, 2012

By Victor Bredykhin

The report is devoted to the investigation and improvement of processes taking place at contact of large quantities of water insoluble liquid and particles of solid phase in a pulp. Theoretical analysis and simulation of acting conditions have allowed to determine that after attaching of oleophilic particles on the «water-reagent» separation surface the break of a formed complex is taking place according to the reagent volume and for oleophobic minerals along the «solid-reagent» separation surface. As a result particles are selectively treated if the magnitude of the reagent adhesion to the surface of solid phase in water is great. The results of dispersion are influenced significantly by availability of sharp edges on the surface of real particles. They keep tree phase perimeter of moistening. It is possible to fix reagent in the form of lens whose contact angle is significantly smaller in comparison to the thermodynamic angle. In adhesion dispersion the reduction of reagent volume, covering the equal area of particles surface is possible when the reagent is in a pulp in the form of thin films on the «water-gas» separation border. The process is tested in laboratory conditions as well as at pilot concentrating mills in flotation of sulfide ores, non-ferrous metals (copper-molybdenum ore), native sulfur and coal.

Jan 1, 2006

By Moo Eob Choi

A new process for converting sulfur dioxide to elemental sulfur by a cyclic process involving calcium sulfide and calcium sulfate without generating secondary pollutants was developed at the University of Utah. In this process, sulfur dioxide is reacted with calcium sulfide to produce elemental sulfur and calcium sulfate. The latter is reduced by hydrogen to regenerate calcium sulfide. In the present work, the effects of different pelletization conditions for the initial reactant calcium sulfate on the strength and reactivity of the pellets were determined. These conditions include the type, amount, and impregnation method of catalyst, binder amount, and sintering. Experiments were also performed to determine the effects of temperature in the range of 973-1173 K, pellet size, cycle repetition, and water vapor or carbon dioxide content in sulfur dioxide stream on the reaction rates of the cyclic process. Nickel-catalyzed fired pellets produced by the use of molasses or cement as a binder showed good reactivity as well as high compressive strength during the cyclic tests. The binder amount did not significantly affect the reaction rate.

Jan 1, 2006

By Daniel Kittelty

A fully instrumented laboratory electrowinning cell has been used to produce nickel cathodes from synthetic solutions containing various impurities in order to evaluate the effects of both metallic ions and organic reagents (from prior solvent extraction and other processes) on the quality of the electrodeposited nickel. The conditions used were typical of those employed in industrial electrowinning operations. The impurities were found to alter the crystal size and shape, induce the development of hydrogen pits on the deposit surface, incorporate as metal hydroxide crystals in the deposit, and alter the internal stress and current efficiency. These effects have been interpreted in terms of previously established relationships between the solution composition and the physical properties of the cathodes. The incorporation of the common metal impurity ions into the deposit have been interpreted in terms of a mass transport controlled reduction or precipitation reactions. In particular, a low concentration of aluminium ions resulted in an initial highly deleterious effect, which was replaced by a positive influence at higher concentrations. A model which involves the buffering effect of the aluminium on the pH at the cathode surface has been proposed.

Jan 1, 2003

By Matthew Jeffrey

Leaching, cementation, electroplating and flotation are all electrochemical phenomenon. They are also key processes in the hydrometallurgical treatment of metals. Unfortunately electrochemical methods tend to be under-utilized when studying these processes and one possible reason for this is the confusion surrounding the large number of electrochemical techniques available. In this paper four former PhD students of Professor Ian Ritchie present an insight into how one electrochemical technique can be used to compliment rate/kinetic studies. The paper details how to perform the experiments, interpret data, and recognize complications with the results. Examples where this approach has been highly successful are presented, and include: cementation of zinc by aluminium, cementation of copper by nickel, cyanide leaching of gold and the cementation of gold thiourea by mild steel. The examples illustrate that this universal approach adopted by Ian Ritchie provides the key to understanding the mechanism of many hydrometallurgical reactions.

Jan 1, 2003

By E. Allaine

Carbochlorination kinetics of pure MoO3, Nb2O5, Ta2O5 and V2O5, by Cl2+CO+N2 gas mixtures was investigated between 380 and 1000 °C. Standard free energy of carhochlorination reactions and phase stability diagrams of these refractory metal compounds were calculated. The influence of total gas flow rate, temperature, reactants partial pressures on the reactivity of these oxides were investigated. The apparent activation energies were found to be about 83, 75, 110 and 100 kJ/mole below 650°C for MoO3, Nb2O5, Ta2O5 and V2O5, respectively. Above this temperature, the Arrhenius plots exhibit a rate anomaly attributed to thermal decomposition of COCl2 and/or structural changes of these refractory metal oxides. The apparent reaction order of carbochlorination of these oxides with respect to Cl2+CO was determined. For these refractory metal oxides, the reaction rate was maximum for a Cl2/CO ratio of about 1 in the chlorinating gas mixture. Results of carbochlorination of these oxides are compared and discussed.

Jan 1, 1995

By Guojun Ma

The entrainment of charge materials, evaporation or volatilization of elements and ejection of slag and metal by spitting or the bursting of gas bubbles are mechanisms whereby stainless steel plant dust are generated from the electric arc furnace and refining converter. TCLP and ASTM D 3987-85 tests on dust that was collected from the baghouse filter system of a South African Stainless Steel plant showed that this dust can be considered hazardous according to South African legislation, due to the high degree of Cr (VI) leachability (~13mg/l for TCLP and ~8mg/l for ASTM vs. regulation threshold of 0.05mg/l in drinking water). The dust is therefore considered to be harmful to both the environment and human health, due to its high solubility in water and carcinogenic properties. It should therefore be treated before being stockpiled or land filled. This paper consequently describes an investigation into the formation of Cr(VI)-containing stainless steel plant dust and the stabilisation thereof in a sintering process, whereby the dust was mixed with a silica-rich clay. It is postulated that Cr(VI) form when the (Mg,Fe,Mn,Cr)3O4spinel phase, CaO, Ca(OH)2 and CaF2 (all of which are present in the dust) react. This reaction was found to take place both at ambient and at high temperatures (1100°C). Stabilization of Cr(VI) in the dust could be achieved at an optimum sintering temperature of 1100°C for a 50mass% dust : 50mass% clay mixture. Chromium emission during the sintering process was found to be low, and within environmental limits.

Jan 1, 2006

By A. D. Neuman, C. C. Davis, M. R. Lopez, A. C. Martinez, T. A. Nothwang, S. L. Voit

"One of the thrust areas for the Global Nuclear Energy Partnership (GNEP) program is the development of actinide bearing fuels for transmutation in a fast reactor. Mixed Oxide (MOX) fuel has an extensive fast reactor irradiation history and thus is being considered for use as a baseline composition from which minor actinides (MA) can be incorporated for use as a transmutation fuel. This study involves characterization of precursor powders and pellets to be inserted into the Advanced Test Reactor in Idaho. These pellets will have three compositions: one standard MOX composition, (U80Pu20)O1.98, and two compositions of MA-MOX with oxygen to metal ratios (O/M) of (U75Pu20Am3Np2)O1.98 and (U75Pu20Am3Np2)O1.95. The precursor powders, which consisted of, highly enriched uranium oxide, HEUO2, depleted uranium oxide, DUO2, neptunium oxide, NpO2, americium oxide, AmO2, and plutonium oxide, PuO2, were characterized using a field emission gun scanning electron microscope (FEG-SEM) for particle morphology, size, and size distribution prior to pellet production.IntroductionThe Global Nuclear Energy Partnership (GNEP) was created in order for “fuel-cycle supplier” nations to provide assured supplies of nuclear fuel to “fuel-cycle customer” nations. The customer nations would utilize the fuel for electricity generation and subsequently return it to the supplier nation after it is spent. This spent fuel would then be reprocessed by the supplier nation in order to recycle the actinide constituents, mainly uranium and plutonium, in advanced nuclear power reactors, and thus reducing waste volumes [1, 2]. Nuclear materials would also be strictly controlled through the International Atomic Energy Agency. One of the thrust areas for the GNEP program is the development of these actinide bearing fuels for transmutation in a fast reactor under the U.S. Advanced Fuel Cycle Initiative (AFCI) in order to transmute long-lived transuranic actinide isotopes into shorter-lived fission products [3]."

Jan 1, 2008

By Alex Moyano

The Peirce-Smith converters are traditionally carrying out the converting process of a copper matte in the smelters of Codelco-Chile. However, its production increment is very limited due to the investment magnitude associated to the fulfillment of the environmental regulation. The objective of this paper is to present the Codelco continuous converting process technological advance when converting mattes and/or white metal into blister copper in a Teniente converter unit as an alternative to increment the corporative anode copper production. In 1994, Codelco-Chile started evaluating its ?home made technology? as an alternative to the traditional batch-type converting process. By the year 2001, the Caletones smelter converted liquid white metal to blister copper in a rearranged PS converter continuously. Then, during the 2001-2003 period, several pilot and industrial scale tests were done in a Teniente converter unit at Codelco Norte smelter, evaluating the continuous converting process, i.e., processing liquid mattes (62-68% Cu) to blister copper, demonstrating its technical feasibility with: (i) both constant production of gas flow and SO2 concentration, (ii) production of liquid slag, and (iii) production of a clean blister copper, suitable for the refining process. The promising results have led Codelco-Chile to plan for the 2006 period, a next advanced stage for the continuous converting process evaluation by carrying out a new campaign of tests in a Teniente converter unit at the Codelco Norte smelter.

Jan 1, 2006

By Fiseha Tesfaye, Pekka Taskinen

"A thermodynamic study of the equilibrium phase assemblage AgBi3S5-Bi2S3-S was made by an EMF-technique, using the RbAg4l5 solid electrolyte. The ternary phase was synthesized from the pure Ag2S and Bi2S3 in an evacuated silica ampoule and grinded into powder and mixed with appropriate compositions of B12S3 and S, in a series of experiments, for pressing in to pellets. The pellets were assembled to form the galvanic cells Pt (-) | Ag ] RbAg4ls | AgBi3S5+ Bi2S3 + S + (C) I Pt (+). The EMF-measurements were made in the temperature range 299 - 460 K.In this paper, thermodynamic functions of the ternary phase AgBi3S5 (pavonite) have been determined. The agreement between the obtained results and the literature values were established.IntroductionThe complex group of ore minerals constitutes from trace amounts to a major proportions of sulfosalts. Although the sulfosalts rarely form massive ore bodies, they are commonly associated with rich sulfide ore minerals for the base and precious metals and widely distributed in a metal poor sulfide minerals [1]. For instance, Ag-bearing sulfosalts are encountered in ore minerals for the production of the base metals and are common sources of silver. Nevertheless, thermodynamic properties of the sulfosalts are poorly known.Reliable thermochemical data are essential for quantitative modeling of the chemical behavior of the sulfosalts in equilibrium with sulfides, which in turn would promote the optimization of complex minerals treatment and extractive metallurgy of the valuable metals."

Jan 1, 2012

By KNona C. Liddell

The time and spatial dependence of component and species concentrations during in situ uraninite leaching have been modeled using a reactive transport model based on partial equilibrium between reactive minerals and the solution. The flow field is represented by mixing cells in series. The effects of the H2O2, (NH4)2CO3, and NH4HCO3 component concentrations have been simulated, and results are presented for a one-dimensional flow field.

Jan 1, 1995

By K. A. Natarajan

Microbe-mineral interactions in the leaching of complex sulfides are discussed with respect to (a) role of galvanic interactions in selective dissolution, (b) bacterial attachment to sulfide mineral substrates and (c) the utility of specially adapted metal tolerant bacterial strains. Experimental results obtained in the leaching of two types of complex sulfides, namely, a lead-zinc-copper sulfide and a copper-nickel sulfide are illustrated.

Jan 1, 1985

By G. J. Shiflet

This paper will review work done in our laboratory on the formation, thermodynamics and crystallization of aluminum based metallic glass with the addition of rare earth elements. The results demonstrate that the metallic glasses are truly amorphous and not microcrystalline and that they are unusual in their formation because the alloys contain 90 at. % aluminum and there is no deep eutectic present in the phase diagram. Tensile strengths that exceed 900 MPa are obtained for several of the compositions and exceed 1000 MPa after partial crystallization.

Jan 1, 1992

By L. Cifuentes

Electrodialysis (ED), i.e. a technique based on the effects of electrically charged membranes on ions in solution in an electric field, has been applied to Cu-Fe-As-Sb- H2SO4 electrolytes similar to those used in copper electrorefining and electrowinning operations. The effects of current density, time and species concentration have been studied in a batch ED cell. The technique has shown to be effective in concentrating and separating a range of ions and points to possible new methods of treating copper electrometallurgy effluents.

Jan 1, 1999

By Steven E. Follin

In-situ leaching is commonly used to recover uranium from low-grade deposits in sandstone formations. Acceptable recovery rates can only be obtained if the formation retains its permeability during leaching. Field experiences indicate that microbial growth, stimulated by the leaching pro- cess, can cause plugging problems. To investigate this hypothesis, leach solution and solid samples from well casings and submersible pumps were obtained from four in-situ mining sites. Chemical and microbiological analyses were performed. Bacillus species, Micrococcus species, pseudomonads, and xanthomonads were isolated from these samples. A mixed culture of these organisms was inoculated into a uranium core that was being leached in the laboratory. The permeability of this ore sample decreased to one-third its original value after 16 days. The addition of hydrogen peroxide (0.2 g L-1) to the leach solution killed the microbes and restored the permeability to its original value. This suggests that periodic injection of hydrogen peroxide into production wells may reduce microbial plugging in these wells and the immediate surrounding formation.

Jan 1, 1985

By R. A. Sharma

Neodymium metal was successfully produced by the reduction of Nd203 with Na in the presence of CaC12-NaCl melts by the overall reduction reaction Nd203 + 3 CaC12 + 6 Na ? 2 Nd + 3 CaO + 6 NaCl at -750°C. The metal produced was extracted from the salt media by dissolving it in a Nd-Fe alloy pool. The yield (percentage of theoretical neodymium produced) was found to depend on the salt composition and the mass ratio of salt to neodymium in the reactor. A yield of 95% was obtained with salt ratios as low as 3.5. Further decrease in the salt ratio below 3.25 decreased the yield. Stirrer position had little effect on yield; while increasing the temperature and placing fins in the reactor increased the yield. The Nd-Fe alloy produced was of as good quality as that produced using Ca reductant, and was suitable for direct use in producing General Motors MAGNEQUENCH? alloy for permanent magnets.

Jan 1, 1989

By P. A. Olubambi

The effect of ore mineralogy on the bioleaching of metals from complex sulphides was studied by investigating the bioleaching of zinc and copper from a bulk complex sulphide ore from Ishiagu, Nigeria, using mixed cultures of Thiobacillus ferrooxidans, Thiobacillus thiooxidans and Leptospirillum in mechanically stirred reactors at varying particle sizes. Mineral phases within the varied particle sizes of -53, 53, 75 and 106µm were identified using X-Ray Diffraction (XRD), while the elemental distribution within the varied particles sizes was determined by X-Ray Fluorescence (XRF) and Optical Emission Spectrometry using Inductively Coupled Plasma- Optical Emission Spectrometer (ICP-OES). Bulk ore and the leached residues were examined by X-Ray Diffraction. The highest bioleaching recoveries were obtained at particle size of 75µm, while particle size of 106µm gave the least recoveries. Lower recoveries at particle sizes of 53 and -53µm were as a result of their higher silica and siderite content which affects pH, iron mobility and oxidation.

Jan 1, 2006