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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 Hong Yong Sohn

On the occasion of this symposium in my name, I reflect upon the contributions of my academic mentors and early associates who helped shape my professional career. I was fortunate to have these people around me during my graduate work and at the start of my professional career. In forming my view of the technical field and career, they represented academia, research institutions, industry, and different parts of the world.

Jan 1, 2006

By Md Sazzadur Rahman

Electrochemical Impedance Spectroscopy studies were conducted on two organic thermal energy storage materials; Neopentylglycol (NPG) and 2-Amino-2-Methyl-1,3-Propanediol (AMPL). The ionic conductivities and dielectric relaxation times in the low temperature ordered a-phase (monoclinic for both NPG and AMPL) as well as high temperature orientationally disordered cubic y-phase are reported.

Jan 1, 2006

By Ramiro Escudero

Michoacan?s beach sands with interesting concentrations of ilmenite were studied to produce titanium by hydrometallurgical techniques. Nevertheless, among titanium species, there are different additional components of Michoacan?s beach sands which could be of interesting applications. Some of them are likely to be applied for the manufacture of nanocrystalline ceramics. Although, the most applied mineral dressing to treat these kind of sands, that contain magnetic species (i.e., ilmenite, magnetite), is a combination of gravity separation and magnetic separation, it could be of a great deal of benefit to apply the information regarding the surface characteristics of the sands? components, in order to study the application of flotation technologies to separate selectively those species with commercial value.

Jan 1, 2006

By Steven Wright

BHP Billiton?s Olympic Dam copper flash smelter employs the direct to blister process for smelting high grade copper concentrates. SO2 evolution during tapping gives rise to safety concerns. A thermodynamic model for the blister copper (Cu-Fe-S-O) was used to predict the volumes of SO2 evolved. The Multiple Phase Equilibria Model (MPE) was used to evaluate the slag chemistry inside the furnace. The blister copper model was used to explore the relationship between %S and %O in the copper and the amount of SO2 evolved on cooling. The volume of SO2 evolved was sensitive to the O content with reduction to levels below 0.2 ? 0.15% likely to suppress SO2evolution on cooling. Concentrations of S and O in copper samples from trials generally lay above the equilibrium line calculated for an average temperature of 1275C and a partial pressure of SO2 of 1 atm. Consequently there is a thermodynamic driving force for SO2evolution when cooling to this temperature during tapping. A number of potential process options to suppress SO2 evolution on tapping were investigated thermodynamically. Some of the options require treatment of the blister in a forehearth or separate furnace, while others impact on current practises in the flash furnace with slag present. The opportunities that these options present are discussed.

Jan 1, 2006

By S. V. Subramanian

The tool material and the machine design for high speed machining are well advanced over the last decade but the steel design has lagged behind. The paper examines the design of steel in order to control the sliding tribology for high speed machining under dry machining conditions. In high speed machining of steel, accelerated chemical wear of the tool occurs once atomic contact is established at the tool-chip interface, resulting in poor tool life even with high performance tools such as cubic boron nitride. Recent research has confirmed the occurrence of nanocrystalline grains in the interfacial layer of the chip at the tool-chip contact. The volume percentage of grain boundary is increased significantly (10 to 30%) as the nanocrystalline grain size is decreased well below 30 nm. The solubility of tool material into the nanocrystalline grain boundary is two or three orders of magnitude greater than in the crystal lattice. Further the kinetics of diffusion in the grain boundary is seven or eight orders of magnitude greater than in the crystal lattice. Enhanced nanocrystalline grain boundary diffusion occurring in the interfacial layer at the tool-chip contact causes the accelerated chemical wear. Significant improvement in tool life could be achieved by engineering glassy oxide inclusions in steel, designed to self-lubricate the tool-chip interface in-situ at higher cutting speeds. Thus the control of sliding tribological condition at the tool-chip interface is key to suppress nanocrystalline layer formation at the tool-chip contact and hence prevent accelerated chemical tool wear. Sulfide inclusions are designed essentially to promote chip fracture. In addition, sulfide inclusions are designed to act as a diffusion barrier at the tool-chip interface. The application of inclusion engineering concepts to enhance the tool life in high speed machining will be demonstrated with a suitable case history.

Jan 1, 2006

By Leszek Blacha

Since several years aog there is noted an increasing importance of the metallurgical vacuum technologies. This refers mainly to the extra furnace steel treatment processes, melting of steel and special alloys in the induction and arc vacuum furnaces, as well as refining processes of nonferrous metals. In the presented work, there is discussed a phenomenon of evaporation of volatile components of metal bath under reduced pressure with description of kinetics of this process. In this article are presented are the evaluation of the mass transfer coefficients in the melt and gaseous phase. Based on results of our own research on removal rate of impurities from liquid copper (bismuth, lead) in vacuum refining process, it is determined the thickness of hypothetical boundary layer in the gas phase. This allowed to formulate a general kinetic equation defining the evaporation rate of gaseous components from metal bath. The values of mass transfer coefficients determined from this equation were compared with experimental results by other authors working on the evaporation effect of melt components of metal alloys.

Jan 1, 2006

By T. I. Arbuzova

The present work presents the original data concerning using a high pressure torsion method and a shock wave loading technique to produce compact oxide nanomaterials and investigations of the effect of severe plastic deformation on a microstructure, crystal lattice and stability of these compounds. This allowed us to compare two ways of deformation action that can be characterized as quasi-static and dynamic effect, correspondingly. Particular attention was paid to a stoichiometry and surface composition changes upon severe plastic deformations. A procedure for studying chemistry of the oxide nanomaterials by means of nuclear microanalysis and Rutherford back scattering has been worked through. For surface studies the X-ray photoelectron spectroscopy has been used. It was shown that both distortion methods permit to produce massive nano-scale oxide materials from the coarse-grained powder during a single technological cycle. Bulk nanocrystalline materials based on LaMnO3, TiOy and ZrO2:Y2O3 were obtained by the quasi-static deformation technique. Nanoscaled ceramics of CuO, Mn3O4 and LaMnO3 were produced by the dynamic deformations. The density of the nanoceramics comes to 99%. Size effects and specific imperfection of the nanoceramics obtained lead to a set of particularities of physical properties.

Jan 1, 2006

By William Bourcier

Geothermal Brines are a significant potential source of valuable minerals and metals. These brines are water that is heated by the natural heat flow from the depths of the earth. Hotter brines, typically with temperatures greater than 120°C, are used to generate electricity. Lower temperature brines are directly used to supply thermal energy to applications such as agriculture, aquaculture and process/domestic heat. The geothermal waters have had intimate and lengthy contact with the layers of the earth?s crust that they flow through, resulting in dissolution of minerals and metals from the rocks, and solution into the hot water. These aqueous solutions can be processed to recover minerals and metals. Some potential products include silica, zinc and lithium, along with other materials. Recovery of minerals and metals from geothermal brines can be viewed as ?solution mining by nature?, followed by application of known or new hydrometallurgical techniques for isolation and purification. This paper discusses the opportunities, the processes, the challenges, the current status, the economics and the potential for recovery of minerals and metals from geothermal brines.

Jan 1, 2006

By Hector M. Henao

There is an increasing trend in the copper smelters to recycle electronic materials, which contain relatively high concentration of precious metals. As a consequence, the amount of precious metals lost in the slag phase is increasing. To determine the portion of the precious metals chemically dissolved and that associated with the mechanically trapped matte in the slag will be a key factor to improve the recovery of those metals. Thus, an experimental study was carried out to determine the distribution of precious metals (Au, Pt, Pd, Rh, Ru) between the equilibrated copper matte and iron-silicate slag phases. The experiments were made in a magnesia crucible at 1573 K and a fixed partial pressure of SO2 of 0.1 atm for the matte grades between 40 and 70 mass% of copper. It was found that the distribution ratios (defined as mass% X in slag/mass% X in matte, where X represents the precious metal) are around 10-2 for Ru, 10-3 for Au, Pt and Pd and 10-4 for Rh. The distribution ratios show a tendency to increase when the grade of matte is increased.

Jan 1, 2006

By Qin Li

An highly active absorbent with oxidization based on fly ash, lime and additives was prepared. Experiments of simultaneous desulphurization and denitrification were carried out using fixture bed and duct injection. The influential factors for the absorptive capacity of the absorbent were studied. The absorptive capacities of 120.7mg for SO2 and 43.7 mg for NOx were achieved at a Ca/(S + N) molar ratio 1.2, respectively, corresponding removal efficiencies of 87% and 76%, while spent absorbent appeared in the form of dry powder. The optimal temperature and humidity of flue gas treated with this process were shown to be approximately 50\\176 and 5% respectively. The mechanism of removal for SO2 and NOx was investigated. In comparison with traditional dry FGD, this process appears to have lower cost, less complicated configuration and simpler disposal of used absorbent. The valuable references can be provided for industrial application by this process. The foreground of application will be vast in China and in the world.

Jan 1, 2006

By Edgar Blanco

A thermodynamic and experimental investigation to develop a new process for converting molybdenite concentrate to molybdenum dioxide by a water-vapor oxidation process was carried out. In addition, the behavior of rhenium and selenium in molybdenum concentrate during the process was investigated. The kinetics of the reaction were determined by measuring the weight change of a sample with time in water vapor at temperatures between 700-1000°C. The results were analyzed by a Shrinking Unreacted Core model under chemical reaction control, which showed an activation energy value of 102 kJ/mol. To determine the behavior of rhenium and selenium, their concentrations in the molybdenum sulfide and the product molybdenum dioxide were measured by the use of ICP. While most rhenium remained with the molybdenum dioxide after the water vapor oxidation, almost all selenium volatilized. These results agree with thermodynamic analysis.

Jan 1, 2006

By Derek Fray

Molten salts have been used for the extraction of metals since the 19th century but, recently, many interesting processes have been investigated using mixtures of molten salts and different cathodic materials. In several existing processes, the cation is simply discharged from melt but, in some cases, complications arise when the electrode potentials of the cations are relatively close. For example, the co-deposition of sodium with aluminium in the Hall-Heroult process is discussed in terms of electrode potentials of the components in the molten electrolyte. Similar considerations will also be given to the anodic reactions with respect to chlorine, oxygen, carbon dioxide or monoxide evolution from chloride-oxide melts. In some cases, the cathodic product interacts with the cathode to produce new and exciting products such as nanotubes from carbon or titanates and reduced titanium oxides from titanium dioxide. Depending on the electrode potentials, it is also possible to completely change the cathodic reaction from discharge of the cation in the salt to ionisation of the anions in the cathode. Examples are given of the reduction of metal oxides to produce metals, high technology alloys and nanomaterials and the cathodic refining of liquid metals.

Jan 1, 2006

By H. Y. Cho

LS-Nikko Copper Inc, has been operating its Onsan copper smelter since 1979. The smelter began its operation with a designed capacity of 80,000 tpa of copper from concentrates and its smelting capacity was increased to 140,000 tpa of copper by modifying the existing line in 1988. The Mitsubishi Continuous Smelting and Converting Process has been operating since 1998 at the initial capacity of 160,000 tpa of copper. In 2002, the smelting capacity of the Onsan smelter has been increased to 426,000 tpa of copper from concentrate. Now the Onsan smelter has plans to increase its smelting capacity to 500,000 tpa of copper from concentrates by 2010. During the expansion work, the modernization of facilities will be accompanied by an increase in smelting capacity, via the Outokumpu process. This paper reviews the brief history of smelting capacity increase in Onsan smelter and its Outokumpu process modernization plans.

Jan 1, 2006

By Wang Yun-yan

In order to examine the adaptability and the kinetics of leaching different gold ores in alkaline thiourea system, six kinds of gold concentrate and/or calcine with different physical and chemical properties were chosen as objects. The leaching behaviors in alkaline thiourea system with high stability, acidic thiourea system and alkaline cyanide system were compared. Changes of phase, surface appearance, particle distribution and specific surface area of six kinds of gold ores before and after leaching were studied in virtue of modern analytic techniques, e.g., XRD, SEM, and so on. The results indicate that alkaline thiourea solution can be used to leach gold ore, for oxidized gold concentrate removed arsenic by microbe pretreatment(4#) the leaching rate of gold is up to 82.68%, such conclusion overthrows the parlance reported that pH value must be less than 1.78, or gold can not dissolve in thiourea solution. Chemical components and phase are related to gold leaching rate, different gold ores are fit for different leaching system, and alkaline thiourea solution is suitable for the pretreated oxidized gold ores with low content of sulfur and in which the main phase was SiO2, phase almost does not change after leaching basically. Generally speaking, when leaching in alkaline thiourea solution, surfaces of gold ores with glaze change greatly to ones with coarseness, distinct trace and holes of corrosion. Particle size decrease and specific surface area increase of gold ores after leaching in alkaline thiourea solution with high stability except gold concentrate of Zhongyuan gold smelter(5#).

Jan 1, 2006

By Manuel Pérez-Tello

An experimental study on the oxidation of chalcopyrite (CuFeS2), pyrite (FeS2), covellite (CuS) and chalcocite (Cu2S) particles was conducted by means of differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) techniques. Oxygen concentration in the process gas was set to 40 and 70% by vol. and a heating rate of 40 °C/min was used. Response variables included: the temperature of incipient reaction, the total exothermic heat of reaction, particle mass, morphology, and mineralogy of the reacted particles. Based on the experimental data and phase stability calculations, reaction mechanisms were proposed to represent the behavior of the particles during oxidation. The reaction mechanisms were verified by X-ray diffraction (XRD) analyses of the oxidized particles, and by thermochemical and mass balance calculations to reproduce the DSC and TGA thermograms. Overall kinetic models were developed to represent the evolution of the exothermic heat of reaction for each mineral as a function of time. Experiments conducted with copper concentrate particles containing the minerals studied suggest that the reaction mechanisms for the individual minerals can be used to represent the oxidation behavior of the copper concentrate particles.

Jan 1, 2006

By Emma Arakelova

?2?2 (98 %) vapour passed through a reactor at 25Pa where a Zn? target was placed at 273K- 373?. Experiments were carried out on a flow- type vacuum device. ?2?2 decomposition on Zn? surface accompanied by formation of a Zn-containing volatile complex which transferred to the gas phase, and Zn? deposited on a substrate at condensation. As the substrate, five sequentially located quartz cylinders were used at 293K- 423 K (?n). Decomposition of the Zn-containing complex on quartz substrates carried out as a first- order reaction. ?The complex decomposition constant (??) increased with the substrate temperature (?n=293 K, ??=7.05 sec-1;?n = 373 K, ?? = 87 sec-1;?n = 423 K, ?? =158 sec-1). ?The complex decomposition constant did not practically vary when the target temperature increased; the complex formation rate increased slightly.

Jan 1, 2006

By David A. Army

Many times, the maintenance professionals have been involved in changes to processes or systems. Often they rely on seat of the pants knowledge to determine whether or not they were successful. More often than not, once our attention has been turned to other endeavors, the initiative has floundered. This paper will describe those measures that can be most effectively used to track and manage the success of implementing an improved Work Management System. However, not only will the paper discuss traditional work indicators, it will also explain how to establish the behaviors in the work place that will ultimately ensure successful implementation. Combined with the discussion on indicators will be a discussion on how to tie them to bottom line results and display them in the form of a scorecard. Actual results will be discussed.

Jan 1, 2006

By Hong Yong Sohn

On the occasion of this symposium in my name, I reflect upon the contributions of my academic mentors and early associates who helped shape my professional career. I was fortunate to have these people around me during my graduate work and at the start of my professional career. In forming my view of the technical field and career, they represented academia, research institutions, industry, and different parts of the world.

Jan 1, 2006

By Gabriella Tranell

In the manganese ferroalloys industry, there is increasing focus on the performance of different carbonaceous materials within the smelting processes. With a developing scarcity of traditional raw materials, new carbon sources are being identified for potential use in the processes. For this purpose, it is important to be able to predict the suitability of different materials in the process. Hence, the effects of both the physical and chemical properties of the carbon material on the reduction kinetics of manganese and silicon from slag to metal, have been investigated using an advanced sessile drop technique. Using this technique, the reaction patterns of SiO2-MnO containing slag droplets in contact with various solid carbon materials (graphites with different properties as well as cokes and charcoals) at 1400 to 1600\\176;C were studied in-situ. In addition, slag and metal reaction products from kinetic experimental series were analysed. From these results, differences in reactivity between various carbon materials and slags were demonstrated and explained. Mechanisms for both manganese and silicon reduction were proposed.

Jan 1, 2006