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By Huang Chao

The thermodynamics analysis on reducing-matting smelting of sulfide ore of lead, antimony and bismuth which use ferric oxide as sulfur fixed agent is first analyzed. Due to the analysis of reaction mechanism, ferric oxide is first reduced to ferrous oxide, then ferrous oxide produce reducing-matting reaction with sulfide ore and reducing agent as reaction equation: MeS+FeO+CO=Me+FeS+CO2. The reaction thermodynamic calculation shows that the reducing-matting reactions of lead sulfide, antimony sulfide, Jamesonite, and bismuth sulfide are feasible, but is infeasible for zinc sulfide. These conclusion provide a feasible method for solve the pollution which produced in the smelting of sulfide ore of lead, antimony and bismuth.

Jan 1, 2006

By Chunlin Chen

Published data on thermodynamics of a number of minor elements (As, Sb, Bi, Pb, Zn, Se, Te, Cr, Sn) in liquid copper, matte and slag have been reviewed, assessed and used in development of thermodynamic solution models of melts. The behavior of antimony in alloys, mattes and slags is used as an example to illustrate the approach taken in assessment of published data and validation of the developed models with respect to the activity of Sb in condensed phases as well as the effects of matte grade, slag chemistry, temperature etc on the equilibrium distribution of Sb between melts and the gas phase. Results obtained from a comparison of different smelting processes with the modeled multi-phase equilibrium are presented and discussed. The predicted effects of slag chemistry and matte grade on the deportment of other minor elements during smelting of copper mattes will be presented and discussed.

Jan 1, 2006

By V. G. Papangelakis

The implementation of a flow-through yttria-stabilized zirconia (YSZ) sensor for pH measurements in high temperature and concentrated electrolyte systems relevant to hydrometallurgical processing of nickeliferous laterites is discussed. Instrumentation involved the use of a custom made flow-through titanium electrochemical cell. Accuracy and validity of the pH measurements at temperatures up to 250C were assessed using concentrated sulphate process solutions ranging from synthetic binary sulphuric acid ? water solutions to progressively multicomponent metal ? sulphate solutions simulating laterite Pressure Acid Leach conditions. The measurements were also compared with theoretical models using recently obtained thermodynamic data. A difference of ±0.25 pH units was observed between measured and calculated pH values at temperatures. This is an acceptable difference given that these are the first direct high temperature pH measurements ever on the concentrated acidic sulphate solutions. This result is encouraging more research for the development of industrial electrochemical systems for direct pH measurements in autoclaves.

Jan 1, 2003

By D. J. Burkhardt

Newer copper SX/EW facilities often incorporate hot water heating for the cell feed electrolyte to obtain the necessary plating temperatures of 40 to 50°C. Heating is most necessary in oxide heap leaching, however it may also be required in bioleaching of secondary sulphides in colder climates or higher altitudes where most of the heat gain in the heap is lost to the environment. Given that the solution flows in the leach, organic circuit and electrolyte circuit are circular in nature, and the fact that the hot lean electrolyte is often exchanged with cooler rich electrolyte, it can be difficult to access the heating requirement for the cell feed. There are energy losses in piping, tankage, raffinate, and energy gains through the PLS and electrowinning process itself; some of these are significant and others are not. This paper discusses the overall heat balance, the relative significance of the various energy gains and losses, and describes a methodology to develop a heat balance to assist the engineer in sizing the heating equipment.

Jan 1, 2003

By Ali Akbar Mottahedi

It is known for a long time that the reaction of oxygen with carbon, silicon, iron and many other elements is exothermic. The heat of released from these kind of reactions can decrease the time of fusion of iron and steel for metallurgical purposes in the electrical arc furnaces. By decreasing the time of fusion, we increase the rate of process and the amount of production. So, by blowing oxygen in to the furnace, we can reduce the consumption of electricity and save cost. There are many problems in the procedure of the oxygen blowing. In this project, the theoretical aspect of the oxygen blowing and its side effects into the arc electric furnaces are investigated. An oxygen blowing system into the arc electrical furnace of metallurgy department of Machine Sazi factory was also set up. This process reduced the consumption of electricity up to 22% and increases the rate of production, by reducing tap ? to ? tap time up to 15%. In this project; all oxygen blowing systems and its control were set up.

Jan 1, 2006

By Takeshi Yoshikawa

For the sake of effective control of titanium-compound inclusions in the steel-making processes, especially for stainless steel production, the influences of alloying elements of chromium, nickel, manganese, molybdenum, copper and oxygen on the thermodynamic property of titanium in molten iron were investigated at 1873K. At a certain titanium potential controlled by the coexistence of Ti3O5 and Ti2O3 doubly saturation of steels, the interaction parameters between alloying elements and titanium in molten iron were determined as follows. [ ] From the investigations on the equilibrium of titanium deoxidation in molten iron, the activity coefficient of titanium and the first order interaction parameter between oxygen and titanium were determined as follows. [ ] Also, deoxidation equilibrium for titanium in molten 304 stainless steel was measured and compared with the calculated results using the determined interaction parameters.

Jan 1, 2006

By R. D. Prengaman

Lead usage in paint, anti-knock gasoline additives, pipes, seals, and solder has declined markedly over the past 30 years. Products utilizing the unique properties of lead and its ability to be recycled have survived and grown. These products include shielding, glass (particularly TV and computer screens), sheet for roofing, stabilizers for PVC, insoluble anodes for metal production, electronic solders and lead acid batteries. With the loss of markets many companies have decreased lead product development efforts. Much of the patent lead materials development is devoted to lead acid batteries. In the past 25 years, the automobile battery has been almost doubled in power and reduced in weight, leading to a nearly three-fold increase in performance. Corrosion-resistant lead alloys and improved battery designs have made battery lead usage more efficient. The same corrosion-resistant battery alloys are utilized to increase the life of electrowinning anodes. The challenge for lead product development is not only to maintain and improve the existing lead products, but also to develop the growing lead acid battery market for telecommunications, uninterruptive power sources, remote area power, hybrid and electric vehicles. Lead

Jan 1, 2000

By Nobuaki Sato

For decontamination of SO2 containing waste gases from industries such as ferrous and non-ferrous metal companies, desulfurization with hydrogen production by the reaction of Br2 and SO2 was proposed as bromine-sulfur (BS) process. In this process, SO2 is fixed as H2SO4 in the presence of Br2 and H2O forming H2SO4 and HBr. Then hydrogen is produced by the decomposition of HBr and Br2 as byproduct is recycled. The reaction of Br2, SO2 and H2O was found not to occur in liquid phase but to occur in vapor one. The production ratios of H2SO4 and HBr showed a maximum at temperatures around 60 oC. The highest production ratio was obtained at 70 oC with a mixing ratio of Br2:SO2:H2O=1:1:10. The experimental results were discussed with thermodynamic consideration.

Jan 1, 2006

By Kejun Liu

Platinum and palladium are usually dissolved together and followed by separation. In this study, the selective leaching of platinum and palladium from a secondary resource, such as dental waste, by using chloride solution (hypochlorite and chlorate) has been developed. Results indicate that about 100% of palladium could be initially extracted by the combination of 0.3 mol/L sodium hypochlorite (NaClO) and 0.068 mol/L sodium chloride (NaCl) at pH 1.2 and 298K in 1.5 hours, or the combination of 0.005 mol/L sodium chlorate (NaClO3) and 6 mol/L hydrochloric acid (HCl) at 298K in 0.5 hour. About 100% of platinum could be extracted from the residue by the combination of 0.47 mol/L sodium chlorate (NaClO3) and 12 mol/L hydrochloric acid (HCl) at 298K in 2 hours.

Jan 1, 2003

By W. John Rankin

Professionals, technical and non-technical, working in the mineral and metal commodity industries need to understand the concept of sustainability and its implications for the industry. Undergraduate courses have not done this well in the past. Much has been written in this field, and there have been great advances in understanding. However, much of what has been published is superficial and sometimes misleading, and there is as yet no coherent, single account that can serve as an introduction or overview for mineral industry graduates. This paper presents an outline which can guide readers in developing an understanding of the topic and its relevance to their work. Key references are provided, particularly those accessible on the internet, which will serve to introduce the reader to the important principles and understandings. The guide should also be useful to academics preparing students to work in the minerals and metal production sectors.

Jan 1, 2010

By Kurt Westerlund

Three. years operating experience of the FLUXFLOW waste heat boiler (WHB) 20.000 nm /h at Boliden Ronnskar Sweden on a TBRC smelting palena (PbS). Operating experience from the Kivset flash WHB 11.900 nm /h at Samim, Porto Vesme, Sardinia, Italy. Conceptual features of the 93.600 nm3 /h FLUXFLOW (WHB) on the Isasmelt smelting in melt furnace for 180.000 t Cu/a at Mount Isa, Australia.

Jan 1, 1992

By M. Pineau, G. A. Monteith, M. Laliberte, G. Houlachi

Conventional physico-chemical treatment methods, either hydroxide or sulfide precipitation, can hardly achieve a high removal of selenium from the liquid effluents which can be generated in some metallurgical operations. In weak acid solutions, selenium exists mainly as anionic species (selenite Se03-2 and selenate SeCV2) which, therefore, cannot precipitate as metal hydroxide or metal sulfide compounds. At the same time, neither selenite nor selenate form stable precipitates with the common cations (Ca, Mg, Fe, etc.) that are typically used in water treatment. At Noranda Inc., CEZinc Division in Valleyfield, Canada, the introduction of new discharge requirements for effluent toxicity initiated a R&D program which resulted in the full-scale implementation of a new treatment method for selenium removal. The goal of this paper is to present this new method which is now being patented by CEZinc. The process chemistry will be presented along with pilot-scale developments and full-scale operational results.

Jan 1, 2000

By Lætitia H. Delmau

SXFIT is the latest in a series of programs developed in our group to model solvent extraction systems of increasing complexity. SXFIT permits the user complete freedom to define the constituents from which the composition of each phase is to be specified in the data and from which all species of a model for a system are assumed to be formed. Activity coefficients in the nonaqueous and aqueous phases, water activity, apparent molar volumes of aqueous species, and solution density needed for the conversion of concentration from the molarity to the molarity scale are all taken into account by the program. Several extraction systems relevant to nuclear-waste treatment were modeled successfully using this program. As an example, the cesium extraction efficiency of the CSSX process chosen by the USDOE for cesium removal from high-level waste stored at the Savannah River Site can be predicted correctly for varying feed composition.

Jan 1, 2003

By Tong Deng

Clean processing of copper converter slags for reclaiming cobalt and copper could be a challenge. An innovative and environmentally benign approach for recovering metal values from such a slag was developed in the present work. Curing the slag with sulfuric acid, without re-smelting or roasting as currently practiced in the industry, made it amenable to leaching, and more than 95% of the cobalt and up to 90% of the copper was extracted, together with iron, by water leaching, leaving silica behind in a residue. Copper in the leach liquor was recovered by cementation with iron, and the dissolved iron crystallized as ferrous sulfate monohydrate. Cobalt in the pregnant solution rich in iron was recovered by either cementation or sulfide precipitation. Chemical and mineralogical characterization of the slag and its products were examined and compared to determine the nature of the changes occurring during curing and leaching. Operating variables were also investigated and optimized.

Jan 1, 2003

By J. A. Sanhueza

The environmental regulations and terms issued by the Chilean Government for all copper concentrate smelters have been a very important reason for permitting project developments that drastically decrease the sulfur emissions due to the pirometallurgycal copper process. A remarkable case of the Hernan Videla Lira Copper smelter, located on the Copiapó Valley and very near some housing-sets of a city of high development, are described. Results of this project's implementation of the control and reduction of off gas emissions, the control and monitoring system, the community conflicts, and the strategy to comply with the demands established by the state environmental institutions, are presented.

Jan 1, 1999

By R. E. Molnar

A number of flowsheets have been designed and operated, or are currently being considered, to extract copper from leach solutions having much more copper than the 4 g/L levels typically found in heap leach liquors. Dealing with these solutions has required that the envelope for ?normal? copper solvent extraction be pushed beyond the usually considered limits. Others have published information on flowsheets to recover copper from leach liquors containing over 25 g/L copper. Secondary solvent extraction circuits are often required to attain satisfactory overall recoveries. This paper reviews some of the issues faced in three pilot plant circuits that were operated by SGS Lakefield Research to produce cathode copper from solutions containing 8 to 20 g/L Cu. The primary objective was to maximize copper extraction using one solvent extraction circuit. The role of feed acidity and the disposition of impurities such as iron and chloride are considered. The challenges of running short SX piloting campaigns are discussed.

Jan 1, 2003

By V. L. Stolyarova

The high-temperature Knudsen effusion method was used to study partial pressures of vapour species, activities of components and the Gibbs free energies in the DyF3-Dy2O3 system at the temperature (1357±5) K. Partial pressures of vapour species were obtained by the ion current comparison method, with the DyF3 partial vapour pressure over pure DyF3 as a standard. The equilibrium constant of the gaseous reaction DyF3 + DyOF = Dy2OF4 is evaluated. Thermodynamic data obtained are in a agreement with the available phase diagram of the DyF3-Dy2O3 system. Results of the present study illustrate the negative deviations from the ideal behaviour in the system.

Jan 1, 1997

By Peng Fan

Nitride capacity is usually employed as the measure of slag?s ability to remove nitrogen from liquid metal, since nitrogen distribution ratio between slag and metal can be calculated from nitride capacity provided that the value of oxygen activity in liquid metal is available. However, during liquid metal refining processes, oxygen activity in liquid metal is usually unknown and thus it is impossible to get nitrogen distribution ratio from nitride capacity under this usual condition. In this paper, thermodynamic analysis indicates that the activity coefficient of nitride in slag can be used to measure slag?s ability to remove nitrogen from liquid metal, because nitrogen distribution ratio between slag and metal can be calculated from the activity coefficient of nitride in slag provided that the content of oxygen potential controlling element like Al in liquid metal is available. Review of reported nitrogen removal studies and our recent study has verified that for a given Al content in metal, the lower the AlN activity coefficient in slag is, the higher the nitrogen distribution ratio. Titanium monoxide based slag has been found to be much more effective to remove nitrogen than other slags. Since Al content in liquid metal is usually available during liquid metal refining processes, AlN seems to be a better measure of slag?s ability to remove nitrogen from liquid metal.

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 B. J. Beaudry

The effect of various levels of purity of the rare earth fluorides and the calcium reductant used to prepare rare earth metals were determined. Metals which have low melting points such as La, Ce, Pr and Nd are not purified by distillation or sublimation. Impurities in the reactants remain as contaminants in these metals. Gd, Tb, Y and Lu which have slightly higher vapor pressures at their melting points than the first four metals are usually distilled to remove the Ta or W impurity introduced by the crucible and are purified slightly with respect to 0 and N by distillation. Rare earth metals that have high vapor pressures such as Sc, Dy, Ho and Er can be purified with respect to 0, N, C, as well as Ta or W by sublimation. The most volatile rare earth metals Sm, Eu, Tm and Yb are readily purified by sublimation and are usually prepared by a reduction-distillation process directly from the oxide. The importance of each step of the processes in determining the final purity of the individual rare earth metals is discussed.

Jan 1, 1989