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By Mao Chen, Baojun Zhao, Zhixiang Cui, Leonel Contreras

Viscosity is one of the important physiochemical properties of metallurgical slags which is important for slag tapping, metal loss in slag, freeze lining and fluid dynamics. High temperature viscosity measurements are time- and cost-consuming and the number of experiments is limited. Viscosity model is an effective way to predict the viscosities of the complex slags at high temperature. However, a reliable viscosity model can only be developed on the base of accurate experimental data. A unique high-temperature viscosity measurement apparatus developed at The University of Queensland enabled accurate viscosity data to be measured for the “FeO”-SiO2-CaO-MgO-Al2O3 system in equilibrium with Fe. An accurate viscosity model has been developed based on Eyring’s theory and extensive viscosity measurements. The viscosities of copper smelting, converting and cleaning slags over a wide range of compositions and temperatures can be predicted and applied in the process control.

Jan 1, 2016

By Tracy T. Morris, Luis G. Navaro

"Anodic copper slimes produced during the electrolytic refining of copper are routinely batch leached to remove copper. At the Amarillo Copper Refinery, an atmospheric leaching process was converted to an autoclave pressure leaching system to improve the removal of copper, reduce the consumption of oxygen, improve leaching times and enhance tellurium recovery. The benefits of pressurized versus atmospheric leaching of slimes were soon realized by obtaining the desired level of decopperization in a shorter time and with lesser quantities of reagents. The autoclave was designed and constructed with a unique oxygen injection system that enables good control of the leaching process and with no plug-ups. Other features include a mass measuring system that balances the quantity of slimes to be leached to the desired final solution concentration based on initial feed concentrations. The end result was a more efficient and controllable leaching process for removing copper from anode slimes.IntroductionThe electrolytic refining of copper consists of an electrolytic cell filled with a sulfiiric acid based electrolyte and pairs of copper anodes and cathodes. When a current is applied, copper in the anode dissolves and is plated onto the cathode. Impurities within the anode that are more noble than copper do not dissolve and end up at the bottom of the cell and are referred to as slimes. Gold and silver are the main slimes constituents of interest because of their monetary value, but there typically are significant quantities of selenium, tellurium, lead, antimony, arsenic, bismuth, nickel, silica and tin. Copper is also present, usually as a metallic or as a reactant with tellurium, selenium, oxygen or sulfur and can range from 10 to 30% of the slimes fall."

Jan 1, 2012

By Kampe. S. L., Baker. Andrew H., Tony Zahrah

"Experimental heats of reaction for the formation of several Al3Ti + TiB2 intermetallic composite formulations have been determined utilizing bomb calorimetry. To overcome the kinetic constraints and achieve ignition in these formulations, a boron (B)/potassium nitrate (KNO3) initiation aid was incorporated within the blended reactant compact. The heat contribution from the initiation aid was regressed to provide estimates of the heat of reaction of the nominal formulations. Powder x-ray diffraction was utilized to identify the products of the reaction and discern any differences between the predicted equilibrium products of the formulation and the actual products.IntroductionReaction synthesis is a technique for the creation of ceramics, intermetallics, and in-situ composite materials [1]. Reaction synthesis is defined by its self, propagating mechanism, where the energy liberated from a localized reaction within a green powder compact is enough to carry the bulk reaction to completion. Achieving a self, propagating state can be achieved in variations of two primary methods of initiation: uniform volumetric heating and directional propagation [2].Uniform volumetric heating involves subjecting a green compact of the unreacted formulation to uniform heating in a furnace to encourage diffusion to initiate the reaction (Figure 1a) throughout the bulk material. Directional propagation utilizes a point heat source at one section of a green compact of unreacted formulation (Figure 1b). The localized exothermic reaction at one point in the compact then initiates the reaction in the section of the compact adjacent to it and fully propagates throughout the entire compact until completion. Initiation of the localized reaction is generally associated with the melting of the constituent with the lowest melting point, with instantaneous initiation of the reaction usually occurring close to that melting point [1]. This melting point can be high in some systems of interest, such as the titanium (Ti) and boron (B) system in equation 1:"

Jan 1, 2011

By Bing Song, Fei Xi, Xuewei Lv, Kai Zhang

The electric arc furnace process is a common method to produce high TiO2 slag from ilmenite. The pre-reduction process was proposed in recent years in order to reduce electricity consumption. In order to enhance the pre-reduction degree, high energy ball milling was proposed to improve the specific surface area of the ilmenite prior to reduction. In this study, the carbothermic reduction behavior of milled ilmenite concentrate was investigated. It was found that the ball milling method can result in a higher reduction rate and improved metallization of iron. The metallization of iron increased with increasing the time of ball milling. The metallization of iron with milling reached 89.49% when the time of ball milling was 70 min., while the FeO content decreased with 70 min. of milling from 11.84% to 4.76%.

Jan 1, 2014

By Wang Dawan

During the process of arsenic bearing gold concentration biooxidation, the content of chloride ion in water is a very important factor to the activity of bacteria and the oxidation of sulfide minerals. In this paper, the influence of underground mine water with different chloride ion content to the biooxidation of arsenic bearing gold concentration and the limit of chloride ion content to bacteria were summarized. These results indicated if the content of chloride ion was less than 1.2g/L, the bacteria?s ability to oxidize sulfide minerals was little affected, and if the content of chloride ion were increased to 2g/L or more, the activity of bacteria was seriously restrained, and if the content of chloride ion were increased to 4g/L, the activity of bacteria was absolutely restrained. So, as the content of chloride ion in water was cumulated to 2g/L or more in biooxidation plant, the water must be refreshed to maintain normal production.

Jan 1, 2008

By Ibrahim Yusufoglu, Cem Kahruman, Mert Zoraga

In this study, a strontium sulfate mineral (celestite) was converted to strontium oxalate in solutions containing ammonium oxalate as a reactant. The experiments were carried out under isothermal conditions. The effects of stirring speed, ammonium oxalate concentration, particle size and temperature on the conversion rate were investigated. During the conversion process, definite volumes of solutions were taken from the reactor after different reaction times for the determination of sulfate ions using ICPOES. Fractional conversions of strontium sulfate were determined at different times and fractional conversion vs time diagrams were generated. It was found that the conversion of strontium sulfate was increased by increasing the ammonium oxalate concentration and temperature in addition to decreasing the particle size. The effect of stirring speed was negligible on the reaction rate. It was observed that above 328 K, a protective layer of strontium oxalate was formed on the strontium sulfate particles. X-ray Powder Diffraction technique was used for characterization of solid substances.

Jan 1, 2014

By Dan A. Mackie

Cyanide leaching operations have taken a beating from the press and the public at large for its seemingly haphazard approach to control of cyanide solutions and containment of tailings. Major spills in Colorado, Guyana, Spain, and more recently, Romania, have highlighted what had already been perceived to be a bad scene. Citizen initiatives and legislative actions are increasing. Whether these indictments are justified or not will not be debated in this paper. What this paper presents is that the technology to avoid these disasters and future ones has been around for more than ten years but has been ignored by the industry, despite demonstrated' cost effectiveness. It is time for miners to wakeup, and use emerging, instead of old, technologies.

Jan 1, 1998

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 H. Bernier

The Noranda Inc., CCR Division, copper refinery located in Montreal-East, Québec, Canada, has expanded over the years to reach a capacity of 410,000 metric tons of cathode production per year. The expansion process resulted in nine, parallel, 200 m. long bays each equipped with its overhead cranes and manually operated washing machines. Anode scrap washing and piling was done manually. The mechanization of the tank house involved the elimination of 18 cells at one end of each of the bays in order to install transfer conveyors where anode scrap and cathode loads are deposited by the bay cranes. The cathode loads are brought by new transverse cranes to new machines where cathodes are washed, piled in predetermined bundle weights, check weighed, strapped then shipped in trucks or railroad cars. Suspension bars are automatically removed, stacked in magazines and sent back to the starting sheet machines. Anode scrap loads are brought to machines located near the anode furnaces where they are washed and piled in bundles for easy charging. The mechanization has eliminated numerous hazardous jobs and has realized a reduction of 0.2 man-hours/ton. After these modifications, the refinery production capacity now stands at 370,000 metric tons per year.

Jan 1, 1987

By Ruben Alvarado

The need to increase business competitiveness while complying with environmental requirements represent the great challenge that the Caletones smelter has decided to face in a new development project with a compromising and willing alliance with its workers. To date, the project is at the feasibility stage, with start up scheduled for the middle of the year 2002. The processing capacity of the Teniente Converters will be increased to levels up to 2400 tpd of chalcopyrite-based concentrates containing 30% Cu, by means of more intensive use of oxygen and improved stabilization of the overall operation. Productivity increses in the converting of white metal and the pyrometallurgical treatment of slag are also planned. As a result of related strategies, the productivity of the supporting facilities, included the capacitiy of the sulfuric acid plants, will be increased. An intensive and well-designed labor-upgrading scheme will allow the transformation of every worker into an expert in his working areas, thus becoming an active driving force in technology development. Mechanization, appropiate infrastructure, and complete process control and instrumentation will give to the skilled and motivated personnel the necessary tools in order to attain the highest potential ever reached with the Teniente technology. The necessary investment for this project based on the adding facilities to the existing plant is only a third of that required to reach the same objective for a greenfield plant, thus yielding a very high return on investment.

Jan 1, 1999

By T. W. Gonzales

The BHP San Manuel Smelter operates an Outokumpu Oy flash furnace, conventional Peirce-Smith converters, anode casting facilities, and two double contact sulfuric acid plants. The flash furnace was commissioned in July 1988 and since then, the smelting capacity has been continuously increased to 30% above design. The converter operation was challenged to process larger amounts of matte with existing capacity. Utilization of industrial technological improvements and people technology transformed the Converter Department from a constraint to easily accommodate the new demonstrated flash furnace capacity. This technology also increased secondary consumption, converter campaign life, and reduced operating costs. This paper will describe the important Converter Department achievements in the past five years.

Jan 1, 1999

By Akira Kaneda

Mitsubishi continuous process employs an electric furnace for settling matte from slag. Electrodes are immersed into the slag layer in the slag-cleaning furnace and the temperature of the melt is maintained at a predetermined level by Joule's heat. Electrodes are immersed to the depth where the current of each electrode is kept at a set value, and they are raised or lowered automatically to compensate for the deviation from it. Because electric resistance of the bath is varied with the matte level in the furnace and the composition and temperature of the slag, the immersion depth of the electrodes is affected by them. Therefore by monitoring the immersion depth and its change with time, abnormal situations in the furnace, such a~ rise of matte level or local abnormal state of melt, can be detected. In this paper, relations between state of the furnace and electrode behavior are discussed based on the plant data, and then a new and simple monitoring method of the condition of the furnace is proposed.

Jan 1, 2001

By Yuzo Hiroshige, Masayuki Kyoi, Tomonori Saeki, Masahide Okamoto, Toru H. Okabe, Yu Miyamoto, Tomohiko Akahori, Takeshi Nemoto

We report Hitachi's approach to establish the recycling process for rare-earth metals in magnet. We have developed a process to disassemble the used electric products to collect the magnets, a process to remove the surface plating film of the magnet, and processes to separate rare-earth metals from the magnet. All processes are operated without chemical solutions in order to minimize the environmental impact due to the waste water emission. For the disassemble process, we have developed an equipment to generate continuous shock on the electric products to loosen screws. A sand blast technique is applied for the plating removal process. Rare earth metals in the magnets are extracted by immersion of the magnets in molten magnesium. The extracted rare-earth metals are separated from Mg by evaporation of Mg. The overall yield of recovery is 86.8 %. The purity of the final rare-earth metal is 98.8 %.

Jan 1, 2014

By Takao Mori

Novel rare earth boron icosahedral compounds are investigated as potential high temperature thermoelectric materials. REB50-type compounds and REB22C2N compounds were synthesized and the thermoelectric properties measured. Seebeck coefficients in excess of 200 V/K are observed at temperatures above 1000 K for the REB50-type compounds. Strikingly, n-type behavior was observed for REB22C2N. Up to now, non-doped B12 icosahedral compounds have all been p-type. The discovery of an n-type compound is extremely important in terms of the potential development of this class of compounds as viable thermoelectric materials. Low thermal conductivities of < 0.03 W/cm/K at room temperature was observed for these rare earth boron cluster compounds.

Jan 1, 2006

By Tatsuki Uzawa, Takashi Nagai

The consumption of Nd and Dy is increasing dramatically because of an exceptionally high demand for Nd-Fe-B-(Dy) magnets and a significant amount of the magnets are wasted. It is important to develop a recycle process the elements from the wasted magnets. In this study, Nd and Dy were extracted from the magnets by silver at high temperature. Nd can be extracted more than 70 % by silver. However, Dy is extracted only 25 % in the same experimental condition.

Jan 1, 2014

By Kwan Soo Han

A thermodynamic model for predicting the distribution coefficients has been developed by taking into account the extraction mech-.ism and the chloride complexation when Sm, Eu, Gd, Tb, Dy and Ho for single component systems are extracted from acidic chloride solutions by di-2-ethylhexyl phosphoric acid and 2-ethylhexyl phosphonic acid mono-2-ethylhexyl ester in kerosene, respectively. The model equation includes two constants, of which one corresponds to the apparent extraction equilibrium constant and the other is due to the variation of the activity coefficients of organic species. These values are determined from a few experimental data by the curve fitting method Then, the distribution coefficients under untried conditions have been predicted from only the initial data by iterative calculations. Bromley&apos;s formulation is used to estimate the activity coefficients of aqueous species and the interaction parameters for some rare earth chlorides are reported in terms of molality and molarity using data from Spedding et al. The validity of this method has been confirmed by excellent agreement between the experimental and the predicted distribution coefficients.

Jan 1, 1989

By Oleksandr Liaskovskiy, Sergey Beringov, Sergiy Yatsuk, Timur Vlasenko, Iryna Buchovska

"Working with solar-grade silicon for solar cells application usually meets some difficulties in comparison to polysilicon produced by Siemens method: higher impurities content leads to lower yield, worse electro-physical parameters and poor performance in solar cells application. However some adjustments in ingot production can show significant improvements in quality of final product: crystalline wafers and cells.Recent investigations have shown that solar-grade silicon is suitable for high effective production process such as mono-like multicrystalline wafer production. Production-scale lots made at Pillar show promising results for solar-grade silicon application: high-quality wafers with significantly big crystalline grains of <100> orientation.IntroductionThe standard technology of producing multicrystalline silicon ingots by directional solidification method in quartz crucibles has a number of disadvantages resulting in limited efficiency of solar cells made of multicrystalline material: crystallites of multicrystalline ingot are relatively small (down to 5 mm size), grain borders of crystallites contain parasitic impurities such as metals, silicon nitride etc., crystallographic orientation of crystallites is random. The listed deficiencies are an integral characteristic of the technology which affects the efficiency of solar cells, such as presence of solar cells with low efficiency even at a high level of average efficiency, problems with shunted cells, silicon nitride inclusions, which adversely affect cell efficiency and are centres for silicon carbide formation, impossibility of application of high effective alkaline texturing etc. Also with regard to the targets set by photovoltaic to reduce the cost per Wp in the nearest future, standard technology of multicrystalline silicon ingots production by directional solidification faces certain challenges some of which are hard to overcome due to rather low efficiency of solar cells made of multicrystalline wafers. Therefore alternative methods of multicrystalline silicon production for photovoltaic application having a number of advantages in comparison to traditional technology are developing rapidly."

Jan 1, 2012

By Hans von Michaelis

There has been a renaissance in gold and silver extraction and recovery that has taken place over the last fifteen years, since the price of gold was freed from the $3510~ level. Despite major advances in such areas as carbon adsorption processes for gold recovery, refractory gold ore treatment, crushing and grinding, process control, etc., there still remain several gold and silver mineral processing frontiers. Frontiers related to environmental management present significant challenges especially in the USA. More than ever it is appropriate to optimize total economics by adopting a "systems approach" that integrates mining, mineral processing and environmental management.

Jan 1, 1993

By Asmo Vartiainen

The viscosity of liquid Fe-O-SiO2 -slag at copper smelting conditions was investigated using a rotational viscometer. The studied parameters were oxygen partial pressure (10" °-10"6 bar ); composition of slag (Fe/SiO2 ratio), and temperature (1250-1400°C). The viscosity values are presented as a function of Fe/SiO2 ratio and as isoviscosity curves in ternary FeO-Fe2O3-SiO2 diagrams. The increase in viscosity at high silica contents can be accounted for the polymerisation effect of SiO4/4- -anions. At high ferric iron contents, higher oxygen partial pressure, the viscosity values increase especially near the magnetite saturation. The viscosity values are highest at the double saturation of silica and magnetite. At lower silica and ferric iron contents the viscosity values are more uniform in the homogenous liquid slag area. The viscosity values were lowest at high temperatures and highest at low temperatures.

Jan 1, 1998

By Maria D. Salazar-Villalpando, Anthony Cugini, Bryan Reyes

"The electrochemical reduction of CO2 was performed in a laboratory-made, divided Htype cell. A copper electrode was used as the cathode. An Aldrich Nafion 117-type ion exchange membrane (0.18mm thickness) was used as the diaphragm. NaHCO3 and KHCO3 were studied as the catholytes. Hydrogen evolution from water reduction and products from CO2 electrochemical conversion were recorded. Higher CO2 reduction enhancement was observed by KHCO3 as compared to NaHCO3. The main conclusion of this work is that in fact CO2 can be electrochemically reduced with copper electrodes.1.-INTRODUCTIONThe direct electrochemical reduction of CO2 may allow for a simple process and, by avoiding high temperature reactors, would enable the process production rate to be quickly varied to follow the time of day availability of surplus electricity [1]. Temperature has a major effect on the electrochemical conversion of CO2 since its solubility increases when temperature decreases [2]. The electrical potential applied to the electrochemical reacting system will have an influence on the product distribution, as well. For example, a narrow potential range during cyclo-voltagraphic studies will determine the detection of a lower number of products. A recommended potential range to study the electrochemical reduction of CO2 is -2V to 2V. Moreover, the reaction rate on the electrode is governed by various processes, such as the kinetics of electron transfer, adsorption/desorption at the electrode surface, and diffusion of CO2 to the Cu electrode. The availability of active species, CO2 for electro-reduction, is extremely low at the vicinity of the electrode surface and it seriously interferes with the rate of mass transfer. In batch type electrolytic reactors, depletion of CO2 at the surface takes place first. CO2 from the bulk then has to diffuse to the electrode surface, resulting in mass transfer controlled kinetic phenomena. During the above process, several other competitive side reactions could suppress the primary reaction even though the cathode has good electro catalytic properties for reduction of carbon dioxide. When the dynamic supply of specific active species is ensured to electrode surface, the mass transfer effects are minimized to certain extent. Hence it is envisaged that a continuous flow reactor is more efficient for the electro-reduction of CO2 in CO2 saturated aqueous electrolytes. The primary reactions that occur at the copper electrode during the reduction of CO2 are listed below (with the standard potentials calculated using formation energies [1] :"

Jan 1, 2010