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By Michael S. Moats, Alexander Derrick

"The Winand Diagram was developed and has been used for decades to illustrate the interaction between polarization, mass transport and inhibition on the resulting structure of a metal electrodeposit. Recently, Adcock et al. criticized the Winand Diagram and developed their own structural diagram based on nucleation and plating overpotentials. Their work was based on zinc electrodeposition using a galvanostatic staircase method. This work explores the nucleation and plating overpotentials for copper electrodeposition using conditions typical for primary electrowinning and the galvanostatic staircase experimental technique. Additionally, the effects of organic additives and plating substrate on these overpotentials are reported.IntroductionThe control of electrodeposited structures is critically important to modem electrometallurgy operations to insure proper quality and efficient energy use. Electrodeposition of base metals for primary recovery (e.g. electrowinning or electrorefining), while similar to plating for decorative or device manufacturing, differs in the need to produce deposits that cover large areas and grow to significant thickness. Thus, controlling nucleation and particularly growth of electrodeposits is critically important for base metal electrometallurgical operations.The control of nucleation and growth on an industrial scale is most influenced by five parameters - current density, temperature, metal concentration, electrolyte agitation and additives. The effects of these parameters on electrodeposition are interrelated. To describe their effects on the type ofelectrodeposits generated and provide practitioners with a useful tool, Winand developed what is known as the Winand Diagram [1-2]. An adapted version of the Winand Diagram is shown in Figure 1.Winand characterized electrodeposits using Fischer's classification [3] and plotted the various deposit types versus inhibition on a vertical axis and the ratio of current density to bulk metal concentration on the horizontal axis. Inhibition intensity is a complex parameter and is still not well understood even though Fischer introduced the term in 1960 [4]. Often, inhibition intensity is simplified to equal the concentration of organic additive at the deposit surface and is related to the inverse of the exchange current density of the metal being deposited. The ratio of current density to bulk metal concentration is used to represent the ratio of crystallization overvoltage to mass transport of the depositing ion. As such i/iL could also be along the horizontal axis, where iL is the limiting current density of the electrodeposition reaction."

Jan 1, 2012

By Zheng Wei, Jian Cheni, Zhenliang Weng, Wei Liang, Hongbo Zhu, Jinhui Peng, Linqing Dai, Qianxu Ye

"By testing the dielectric constant and the dielectric loss factor of concentrated Dahongshan, mill scale, anthracite and light-burned dolomite in different frequency and temperature, and by studying the temperature-rising characteristics of the materials in the microwave field of 2.45GHz in frequency, the research in the paper shows that to reach at 1250°C under the same condition -2KW the microwave power and 30g the mass --the time concentrated Dahongshan takes is 330s, whereas the millscale is 855s and the anthracite is 820s. About the last one, the higher the temperature is, the stronger the absorptivity is. After the temperature has rose to 400°C, the anthracite's absorptivity increases dramatically. The result of the research would serve as the foundation of the further study on making direct reduced iron by microwave heating.1. IntroductionUnder the microwave fields, materials' dissipation of dielectric bodies would generate thermal effect. Therefore, the dielectric constant and the dielectric loss factor are closely related to materials' ability of absorbing microwave energy-the larger the dielectric constant and the dielectric loss factor are, the stronger the material's ability of absorbing microwave energy is, and the better the thermal effect would be[1-2]. In order to research how to make reduced iron from iron ore fines by microwave heating deeply and systematically, the test of raw materials' dielectric constants and dielectric loss factors are of the essence. What's more, because a mineral' conductivity is influenced by its components and crystal structure[3], it is necessary to study different materials' different temperature-rising characteristics; hence such studies would provide theoretical foundation of further research."

Jan 1, 2012

By Jinxing Ji

The thiosulfate lixiviant system for leaching of gold has been under extensive investigation for nearly two decades and consists of ammonium thiosulfate, copper and ammonia. There are several challenges with this system. The occurrence of ammonia must be taken into account from a health and hygiene aspect in the workplace, and also from an environmental perspective with significant levels of ammonia and copper in the tailings. Copper accelerates the leaching rate but causes excessive thiosulfate degradation. A new lixiviant system that has been investigated consists only of sodium thiosulfate without copper and ammonia. Gold leaching is carried out in an enclosed reactor with slightly elevated oxygen overpressure and temperature. Extensive leaching experiments were carried out to minimize thiosulfate degradation and polythionate formation while maximizing the gold extraction. For the preg-robbing carbonaceous ore sample tested, gold leaching was essentially complete within six hours and the thiosulfate consumption was lower than in the typical ammoniacal thiosulfate system. The gold thiosulfate complex in the pregnant leach solution was found to be quite stable under ambient conditions. This new leaching system has the advantages of being more environmentally friendly, has a shorter residence time, lower thiosulfate consumption, lower oxygen consumption, and is easier to control.

Jan 1, 2003

By Thomas Schemmel, Bertram Kesseiheim, Helge Jansen, Uwe Kreme

"During the last decades the refractory life time of the different aggregates of the secondary aluminium production was improved significantly. However, each repair and installation of refractory material affects the operating schedule and can cause costs in the million range. The downtime of just one melting furnace generate costs of 100.000 to 400.000 $ per day. Besides cooling down of the furnace and its repair, the heating-up procedure accounts for the longest time of the shutdown. Usually, heating-up of low cement or ultra low cement castables takes 120 to 150 hours. In order to reduce such expensive downtimes Refratechnik developed a unique and novel product series: Nanobond. These materials can be heated-up in only a third of the usual time. This paper talks about the theoretical aspects, as well as the mechanical and physical properties and especially practical experience of using Nanobond.Theoretical Aspects and Laboratory ResultsCement containing castables such as RCC, MCC, LCC or ULCC are considered standard in many refractory applications. Over the years a wide range of possible raw materials and practical installation methods were developed. However, all of these cement bonded refractory mixes possess one main important drawback. Such materials are characterized by the hydration of the cement bonding. As a result the physical bonded and the hydraulic water has to be removed in a relatively complicated drying procedure. The hydraulic water specifically demands a very careful and cautious heating up procedure. Most of the dreaded steam explosions can occur at a furnace temperature of approx. 250 oC. [1] To avoid such destructions, the heating-up of a new lined or repaired furnace can be very complex and slow. Depending on the furnace or the casted part a drying time of several days with long curing times are common."

Jan 1, 2012

By Irsan Chandra

It is generally recognized that the gold thiosulfate leaching system requires the presence of copper and ammonia in order for acceptable leaching kinetics to be observed. However, the presence of copper and ammonia complicate the chemistry of the system as thiosulfate is rapidly oxidized by oxygen under these conditions. In addition, the environmental impact of ammonia would need to be considered before the adoption of this system. This paper describes fundamental studies into the thiosulfate oxygen system. The two reagents for this system are thiosulfate and oxygen, and leaching is carried out at pH < 7. It will be shown using electrochemical techniques that both the reduction of oxygen and the oxidation of gold-to-gold thiosulfate are hindered. Thus, if leaching is to work under these conditions, then both half reactions need to be improved. The use of additives, such as thiourea and lead have been shown to dramatically improve the oxidation of gold and the reduction of oxygen respectively. The leaching of gold in the presence of such additives is discussed.

Jan 1, 2003

By Masatsugu Morimitsu

"The novel smart anode, MSA ™, for electrowinning of non-ferrous metals such as copper, zinc, nickel, and cobalt has been developed by thermal decomposition. The smart anode consists of a titanium substrate coated with a catalytic oxide layer which comprises amorphous or less crystalline oxide coatings. The catalytic layer contains an iridium oxide-based mixture or a ruthenium oxide-based mixture. The smart anode provides a remarkable reduction in cell voltage compared to other anodes, e.g., commercially available coated titanium electrodes and lead alloy electrodes. The test data has demonstrated that a maximum voltage reduction by ca. 30% is possible compared to lead alloy anodes. The smart anode also gives some additional merits in suppressing unwanted deposits on the anode; i.e., deposition of MnOOH, Pb02, or CoOOH. The electrowinning with the smart anode is possible to be an environmentally friendly process with less energy consumption and less anode deposits.IntroductionA coated titanium electrode iridium oxide-based or ruthenium oxide-based catalytic layers is well known as an insoluble anode for oxygen or chlorine evolution in industrial electrolysis such as chloro-alkali electrolysis, electrogalvanizing or electrotinning of a steel, a thin film production by electrodeposition such as copper foil production (CFP), water electrolysis, and electrowinning of nonferrous metals. The anode is commercially produced by thermal decomposition of a precursor solution painted on a titanium substrate, and the decomposition is usually performed at 450 °C or more. The obtained catalytic oxide coating formed on the substrate contains crystalline oxide as an active component to oxygen or chlorine evolution. The author of this paper had met a problem of such a crystalline oxide coating in the application of copper foil production; the anode was unable to use for a long period because of a large amount of lead oxide (Pb02) deposited on the anode, and the cell voltage was seen to continuously increase and drastically rise by the accumulated Pb02. In this case, the voltage reduction by replacing a lead alloy anode with the dimensionally stable anode was initially observed, but was gradually lost and disappeared. Therefore, the author of this paper aimed and investigated to suppress the unwanted side reaction on the anode, and finally invented a new class of coating based on an amorphous iridium oxide mixture in 2003 [!]. The invented coating was obtained at a low temperature thermal decomposition, e.g., 360 °C, and the coating consisted of amorphous iridium oxide and amorphous tantalum oxide. This invention achieved that oxygen evolution potential shifted more negative so that the cell voltage was reduced, and no Pb02 was deposited in the electrolyte of CFP [2,3]."

Jan 1, 2012

By Asok Kumar Das

"In steel making ferroalloys occupies a commanding role for production of varied quality of steel. Ferroalloys enable alloying elements such as chromium, silicon, manganese, vanadium etc to be safely and economically introduced into metallurgical processes thus giving certain desirable properties of the alloyed metal. Their importance grew with the progress of the steel metallurgy which implied more diversified alloying elements, in better controlled quantities, in purer steel. The ferroalloy industry became a key supplier to the steel industry. Production of ferroalloys generally involves the use of Electric Arc furnace(EAF) into which raw materials(e.g. various metal ores, quartz, coke, lime etc ) with relatively fluctuating physical compositions are loaded. Due to this, one of the major environmental impacts of producing ferroalloys is the emission of dust and fume from the smelting process. INTRODUCTIONFerro Alloys are essential ingredients used for refining, de-oxidation, desulphurization and alloying addition in the production of different types of steel and hence Ferro Alloy industry forms a back bone of iron and steel in the world. Indian ferro alloy industry is more than 45 years old. It produces most of the bulk ferro alloys and a large number of special ferro alloys. The present installed capacity of the Indian ferro alloy industry is sufficient to meet the requirement of existing level of indigenous steel production of about 46 million tonnes. Revised National Steel Policy – 2008 envisages production of more than 100 million tonnes of steel by the year 2011-12, at proportionate annual growth rate per annum. The focus of the policy is to achieve global competitiveness not only in terms of cost, quality and product-mix but also in terms of global benchmarks of efficiency and productivity. In order to achieve the objectives of National Steel Policy and also to meet the requirement of ferro alloys, the Indian Ferro Alloy Industry has to gear up in terms of enhancement in production capacity, sourcing of raw materials, up gradation of technology, improvement in productivity, automation / mechanization, customer satisfaction etc."

Jan 1, 2008

By Kurt Westerlund

Cooling of hot sticky gases with solids in a circulating fluidized bed called FLUXFLOW is described. Fluxflow is used for gas streams from metallurgical reactors, e.g., Isasmelt copper in Australia and TBRC for lead in Sweden. The features and potential of this technology in metallurgy and waste treatment ie described. The FluxfLow la a new, cost efficient high availability solution to treat hot sticky gases that has made new gas handling and heat recovery flow sheets available to the process industry.

Jan 1, 1994

By M. Kawakami

In the blast furnace, the reduction of iron oxide and gasification of coke occur simultaneously. It is well accepted that the gasification reaction controls the simultaneous reaction. Therefore, it is important to develop highly reactive carbonaceous materials. It is also known that the reaction is accelerated catalytically with the addition of some materials. In the present work, the catalytic effect of iron, nickel and CaO on the gasification of graphite and coke was examined. The catalytic effect of iron, nickel and CaO on the reaction rate of graphite was noticed The effect was larger at lower temperature. At 1373 K, the effect almost vanished. The effect was larger in the order of CaO, iron and nickel. The reaction rate of de-ashed coke increased by the addition of iron and nickel. The effect of iron was larger than that of nickel. The effect was larger at higher temperature, which was contrary to the case of graphite. The reactive surface area increased also by the addition. Therefore, the catalytic effect on reaction rate might be attributable to the increase in the reactive surface area.

Jan 1, 2006

By Funsho K. Ojebuoboh

With several "green" applications in the horizon, bismuth has become an even more important minor metal in the smelting and refining of lead. Smelters with a complex sulfide feed invariably deal with bismuth. Its behavior during the smelting of lead in conventional sinter - blast furnace operation is discussed. Because it readily deports to the lead phase during the refining of lead, its separation from refined lead remained unsatisfactory in early lead production. When commercial requirements of bismuth in lead became more stringent early this century, the procedure whereby calcium and magnesium is used to debismuthise lead was developed. The present conduct of this 1936 process, the Kroll Betterton process, is discussed with emphasis on operational improvements.

Jan 1, 1995

By Jie Li, Liangxing Jiang, Yexiang Liu, Junfeng Gui, Bo Hong, Xiaocong Zhong, Yanqing Lai, Xiaoying Yu

"Pb-based alloys with Pr and Ag were prepared in vacuum electromagnetic induction furnace. The tensile strength, corrosion rate and anodic potential in sulfate solution were measured, and the experimental data were analyzed according to the metallographic phases of alloys, the micromorphology and composition of their oxide films. The results show that, with the addition of Pr, the ultimate tensile strength and corrosion rate of pure lead were increased, and the anodic potential decreased. The extra addition of Ag can improve the properties of alloy further. Comparing with Pb-Ag0.8 alloy which is widely used in zinc electrowinning industry, the ultimate tensile strength of Pb-Ag0.6-Pr2.0 alloy was increased by 31.75%, the anodic potential under 50mA/cm2 was decreased by 30m V.IntroductionIn zinc electrowinning industry, the Pb-Ag (0.5-1.0 wt.%, 0.8wt.% normally) anode is widely used as an insoluble anode['l. It can meet the basic requirements, but still has several problems such as high oxygen evolution over-potential (about 860mV), unsatisfactory corrosion resistance, lead contamination of the cathode product and high consumption of Ag etc.In order to reduce the energy consumption, enhance the corrosion resistance, improve the product quality and reduce the consumption of Ag (or even dispense with it), much research has been done, mainly focusing on Pb-based alloy anodes and Ti-based coated anodes. Detailed investigations have already been carried out on binary alloys (Pb-Ca and Pb-Co), ternary alloys (Pb-Ag-Ca, Pb-Ag-Ti, Pb-Ag-Sn, Pb-Sr-Sn, and Pb-Ca-Sn) and quaternary alloys (Pb-Ca-Sr-Ag, Pb-Ca-Ce-Ag, and Pb-Ag-Sn-Co)[Z-4l, Although these anodes can effectively reduce the consumption of Ag, only the Pb-Co and Pb-Ag-Sn-Co anodes perform well with regard to reducing the anodic potential. However, their complicated manufacturing conditions restrict further commercial use.Besides its application in nonferrous metal electro-winning industry, Pb-based alloy is also used as grid alloy for lead-acid battery, serving as active materials supporter and current collector. In order to enhance the corrosion resistance and deep-cycling performance, reduce the impedance of the corrosion film, the addition of appropriate rare earth elements into anodic grid alloys has become a research focus. Studies proved that RE can enhance the mechanical strength of grids, inhibit the formation of anodic Pb(II) film on the surface of grids and then reduce the impedance of the film[ 10-12l."

Jan 1, 2013

By Yotamu Stephen Rainford Hara

"The study focuses on the reduction mechanisms of copper, cobalt and iron during carbothermic reduction of copper-cobalt mineral sulphide concentrates in the presence of lime, in the temperature range of 1073K and 1273K. We have used three types of mineral concentrates which were derived from froth flotation from the Copperbelt region in Zambia. The reduction mechanisms were studied using thermogravimetric analysis in which selected reactions were stopped at different times for characterising the reaction mechanism using optical microscopy, XRD and SEM-EDX analyses. Using SEM-EDX analysis, we have analysed in details the stages of metallic phase formation during reduction process. Metallic cobalt and iron were embedded into copper, thereby permitting magnetic separation of the reduced metals even though copper is diamagnetic. Methods of preferential reduction of metal values were investigated by analysing the metallic phase formation.IntroductionIn conventional smelting or converting of copper sulphide minerals, metallic copper forms by giving off S02 gas on. Although in terms of overall energy balance the selective oxidation for metal production has major advantages, the process suffers from drawbacks in smelting complex concentrates containing copper, cobalt and iron sulphides minerals and these are: (i) cobalt and iron are oxidised, and consequently cobalt is lost into the slag phase. (ii) The volume of S02 gas produced is in low concentrations, which is insufficient for extracting sulphur or manufacturing sulphuric acid. The release of dilute S02 causes serious environmental pollution. The major cause for the loss of cobalt and iron into the slag, is due to that fact that the oxides of these metals are more stable than their sulphides. Since cobalt and copper are more valuable than iron, reducing conditions are required in a separate slag treatment reactor using electric arc melting for recovering the lost metal oxides from slag. This energy-intensive step makes metal making expensive.During chemical beneficiation of mineral sulphides (Cu2S, CoS, FeS) in the presence oflime (CaO), two types of equilibrium conditions may be set up either by forming CaS under reducing conditions, or by stabilizing CaS04 under oxidising conditions [l]. By comparison in the presence of carbon, CaS and metallic phases form, enabling the recovery of metals from sulphide minerals, which have been investigated by a number of authors [2-9]. During reduction of metal sulphide in the presence of lime and with carbon, it has been proven that the overall reaction le proceeds via two main steps: [5, 8, 9] (i) the anion exchange reaction between metal sulphides (MS) and CaO as shown in equation la, followed by (ii) the reduction of metal oxide (MO) via reaction lb."

Jan 1, 2013

By Chao Zhang, Jian Guo, Chaoquan Yao, Leige Xia, Xinyu Li, Jianliang Zhang

In this research, analytical reagents were used for the sintering experiments. And the sinters were using X-ray diffraction, scanning electron microscope and mineralogical microscope analysis to study the effect mechanism of manganese on the silico-ferrite of calcium and aluminum (SFCA) bonding phase formation during the sintering process. The results indicated that the increasing content of manganese would greatly reduce the content of SFCA, and promote the formation of calcium aluminum silicate and the amount of pores and cracks. The existence of manganese inhibited the silicon form into the SFCA and a great deal of Fe2O3 was participated in the crystal transition to Fe3O4. When the ratio of the added manganese was less than 3% in the mixing, the calcium ferrite was in substantially interleaving corrosion with hematite and magnetite. Both the porosity and silicate glass phase content were low simultaneously, which contributed to the sintering production.

Jan 1, 2015

By Seong-Jong Kim

The formation behavior and corrosion characteristics of anodic oxide films on pure Mg and Mg-AI alloys were investigated focusing on the effects of anodizing potential, Al content, temperature and NaOH concentration. Pure Mg and Mg-AI alloys were anodized for 10 min at 3, 10, 40, and 80 V in NaOH solutions. Mg(OH)2 was generated by an active dissolution reaction at the surface of the specimen and the product was affected by temperature while MgO generation increased with NaOH concentration. Moreover, the current density after anodizing for 10 min at a constant potential decreased with increasing AI content in Mg-AI alloys,

Jan 1, 2003

By Mao Chen, Tim Evans, Zhixing Zhao, Weidong Zhang, Baojun Zhao, Dongqing Wang

High temperature softening behaviours of iron blast furnace feeds (sinter, lump and pellet) have been determined under conditions simulated to the blast furnace. The industrial samples were packed with sandwich structure (coke / ore / coke) in graphite crucibles and 30 CO / 70 Ar gas mixture was blowing directly through the bottom of the crucibles. The displacement and temperature were continuously recorded simultaneously to construct the softening curves. Separated quenching experiments were also carried out at selected temperatures under the same gas atmosphere. The temperatures were selected corresponding to the turning points of the softening curves. The phase assemblages and composition of each phase in quenched samples were analysed by Electron Probe X-ray Microanalysis (EPMA). The proportion of the liquid formed at temperature was obtained from the backscattered electron images. The deformation characteristics of these complex multi-phase materials are shown to be related directly to the phase assemblages of the samples and the microstructures. FactSage was also used to assist the predictions of liquid / solid fractions and their compositions.

Jan 1, 2015

Electrocrystallization studies were conducted in a concentrated acid-copper electrolyte to determine the influence of chloride ions and glue on copper nucleation and on the structure of thin copper layers. Electrochemical experiments allied to SEM and XRD examination were performed to characterize the mechanism of nucleation in the presence of additives at 65°C. Results indicated that most of the copper nucleation from a 83 g dm-3 Cu2+ solution, with 140 g dm-3 of H2SO4 is achieved in a matter of milliseconds, Although the presence of chloride and glue, at the concentration levels tested, does not seem to substantially modify the nucleation mechanism, the morphology, nuclei density and the copper film structure and orientation are changed by the presence of additives and by electrolyte stirring.

Jan 1, 1999

By Z. Zhang, Zongshu Zou, Nan Wang

"Thermodynamic calculation is applied to make an investigation on the equilibrium phase relations and liquids of CaO-SiO2-Al2O3-FeOx system for different temperatures. The calculated results with FactSage6.1 show that the effect of temperature on the the equilibrium phase relations and liquidus of CaO-SiO2-Al2O3-FeOx system and its sub-systems is appreciable. The liquid phase regions enlarge with increasing temperature from 1573K to 1873K, while the primary phase fields reduce distinctly.IntroductionThe main oxide components of vitrified bottom ash slag are CaO, Al2O3, SiO2, Fe2O3, MgO, and Na2O, accounting for more than 90% of the bottom ash by weight[1]. During slag processing, the knowledge of thermodynamic properties and liquidus temperature in the related slag systems is highly required [2, 3], which is not yet available. Through literature survey [4-6], it is clear that the systematic information on the concerned complex slag system is scarce. So far the engineers in the field have to make assumptions of the thermodynamic properties of the simplified oxide system, without taking into consideration the interactions of the different oxide components, which hinders the development of the slag valorization and utilization. In order to provide thermodynamic properties for the application of the vitrified bottom ash, the six-component oxide system (CaO-MgO-Al2O3-SiO2-FeOx-Na2O) is highly required. A preliminary phase diagram of the CaO-MgO-Al2O3-SiO2-FeOx-Na2O system can be obtained from extrapolation of the thermodynamic functions of constituent subsystems such as CaO-SiO2-FeOx-MgO, CaO-SiO2-FeOx-Al2O3, CaO-SiO2-Na2O-MgO and CaO-SiO2-Na2O-Al2O3. In this work, the equilibrium phase relation and liquidus of CaO-SiO2-FeOx-Al2O3 system, one subsystem of the concerned complex slag system, are calculated and the effect of temperature is also discussed."

Jan 1, 2012

By Yuhua Pan

Generic mathematical models have been developed for simulating heat transfer in two types of slag resistance heating electric furnaces for sulphide smelting: i) six-electrode-in-line rectangular furnaces and ii) three-electrode circular furnaces. The models are based on three-dimensional steady-state heat transfer of conduction, convection and radiation. Solidification of liquid slag into solid slag by water-cooling units, for use as freeze lining of furnace walls, is also considered in the models. The developed models are capable of providing predictions with reasonable accuracy for electric furnaces on 1) temperatures in slag, matte, cooling water, freeze lining and other solid regions as well as temperatures at various fluid/solid interfaces, 2) freeze lining thickness, 3) furnace smelting rate and 4) furnace heat loss rate. These computer models are built into executable application programs that are very efficient, with execution time less than one second, and can be easily portable to most computing platforms. This paper describes, as an example, the modelling results on heat transfer in six-electrode furnaces. The major modelling results show that in six-electrode furnaces uniform electric power inputs to the electrodes likely lead to low temperature regions close to slag and matte tapping ends of the furnaces, and the power input and the formation of air gaps between freeze lining and cooling units have significant influences on the thickness of freeze lining maintained by the cooling units.

Jan 1, 2006

By Jannie S. J. van Deventer

Geopolymers are novel engineering materials with the potential to play a highly significant role in the transformation of the construction materials and building products industry in the push towards sustainable development. These materials are formed by activation of industrial aluminosilicate waste materials such as coal ash or blast furnace slag with alkaline solutions. Geopolymers derived from coal ash can exhibit superior mechanical properties and chemical stability when compared to ordinary Portland cement (OPC). The use of waste-based geopolymers can also result in significant (up to 90%) reduction in carbon dioxide emissions when used in cement replacement applications. In addition to the formation of conventional pre-cast products, these high performance mineral binders are ideally suited to use in the encapsulation of mine tailings, immobilization of heavy metals and back-filling of mines due to their chemical stability and resistance to acid attack. A key attribute of geopolymer technology is the robustness and versatility of the manufacturing process; it enables products to be tailor-made from a range of raw material sources (waste and/or virgin) with specific properties for a given application at a competitive cost. Despite these key technical and environmental attributes, it is the ability to add significant value to coal ash or and/ or metallurgical slag waste streams which drives the commercial development and uptake of the technology.

Jan 1, 2006

By P. Ruz

A melt transfer ladle was 3D modeled by means of a mathematical fluid dynamics and heat transfer program. Internal temperature profiles were calculated as a time function for a normal ladle and for a pre-heated refractory lined ladle. It was shown that in a normal ladle the molten metal cools down quickly forming accretions. By using an inner lining there are practically no accretions build up within a typical time of operation. Therefore, by applying a refractory lining to a melt transfer ladle and keeping it at a moderate to high temperature it is possible to reduce cold dope circulation in the smelter.

Jan 1, 1999