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By Ehsan Vahidi, Fereshteh Rashchi, Ataollah Babakhani, Alireza Zakeri

"The synergistic effect of Cyanex 302 on solvent extraction of nickel and cadmium from sulfate solution with D2EHPA diluted in kerosene was investigated with the aim of increasing separation efficiency. Experiments were carried out within a pH range of 0.1-5.0 using sole D2EHPA and D2EHPA-Cyanex 302 mixtures in different ratios. Increasing Cyanex 302 to D2EHPA ratios in the organic phase caused a left shifting of the extraction isotherm of cadmium and a right shifting of the extraction isotherm of nickel. As a result, optimum separation was found with a Cyanex 302 to D2EHPA ratio of 0.1M:0.5M. In the present system, effect of a modifying reagent such as TBP was studied. The influence of various diluents including kerosene and carbon tetrachloride was also investigated.IntroductionBatteries are popular sources of portable energy. Ni-Cd batteries are manufactured in two main groups of small domestic cells and large industrial batteries with 80% being in domestic use. Ni-Cd cells have various uses, for example in cordless electric utensils, cordless telephones, airplane engine starters, and communicational distribution systems [1].Depleted Ni-Cd batteries are classified as hazardous waste since nickel and cadmium are heavy metals and suspected carcinogens. Given the risk associated with uncontrolled disposal, directions for issuing legislation on disposal and recycling of used batteries have been made in industrialized countries [2]. Recycling of Ni-Cd batteries is important from both economic and environmental points of view. Different methods have been used for recycling these wastes through pyrometallurgy [3], biotechnology [4,5], and hydrometallurgy [1,2].Due to the advantages of hydrometallurgical processes, several studies have been implemented on leaching and solvent extraction (SX) of the used Ni-Cd batteries. Leaching of batteries is usually done in sulfate or chloride media; while solvent extraction has been used in different extractants: two-stage solvent extraction by D2EHPA and Cyanex 272 [6]. Solvent extraction of Cd from leach solutions has been studied using various extractants; Cyanex 301 [1], D2EHPA [7], Cyanex 302 [8], Cyanex 923 [9], Cyanex 272, Tops 99, PC88A [10]. Application of phosphorus based extractants for the solvent extraction studies of Ni such as TOPS 99 [11], D2EHPA [12], Cyanex 272 [2], has been investigated. Separation of Cd(ll), Ni(II), and Co(ll) from chloride leach liquor of spent batteries [13], were explored in the earlier studies. Cd extraction with D2EHPA involves co-extraction of both Ni and Co [14], which causes issues in the separation process efficiency."

Jan 1, 2012

By A. R. G. Azevedo, G. C. Xavier

"This work has for objective to identify the soil of the neighborhood Codin located in a lacking area of the urban nucleus of the district of Campos dos Goytacazes - RJ, after the identification the best line was determined for the production of soil-cement blocks. In this area it happens habitational deficit and precarious constructions are also verified. The use of soil cement blocks is considered a cheaper constructive method than the conventional (ceramic block or of concrete), because one of the components of the raw material is abundant (the soil) and the constructions can be erect with certain easiness for collective effort regime. Samples of soil of this area were collected for they be characterized with relationship to the physical and chemical characteristics, with I aid of GPS the community's location it was registered. Identified the soil type, the work began the study of lines they to make possible your use in an economical and safe way. For that were made drained blocks in the format 19,5x10x5 cm, with lines containing the addition of 5% and 10% of cement in volume, and as parameter of quality the absorption of water and the resistance to the compression were measured, following the Norms of ABNT.IntroductionWe know that the use of the soil by the humanity come from the antiquity. And ifs confirmed by the archaeology places of the old civilizations of the word. The most remote constructions date from 10.000 years old in Jericoh, in the Jordan River Valley. This work became more intensive at 3.000 B.C. (Before Christ), by people who lived in those valleys with mood areas, a lot of clay and washed by the rivers.Almost all the sectors of engineering of soils choose the stability to use the local soil. Although, artificially treated, offers more economical advantages.The stability of a soil consist of endow it of the condition to resist the deformations and ruptures during the period that it is being used, because these characteristics are necessary in any construction.The application of the natural soil only is possible in places that they are of good quality and attend to the requirements of engineering to the type of previewed application. The granulemeter correction and the chemical stability include cases of inappropriate soils areas, turning the soil able to be used as construction material. Among the stability agents, usually added to the soil for stability ends, the cement is indicated."

Jan 1, 2013

By Jin-yan TIE, Ke-xin JIAO, Qian Li, Hai-bin ZUO, Jian-Liang Zhang, Meng SHEN

This paper designs three factors such as temperature, pH, conductivity and three levels of orthogonal test. Temperature is a significant factor. However PH and conductivity are not significant through poor analysis. Further research is conducted on the temperature. Temperature stability is 50 . Suitable water velocity is 2.3m/s, which is calculated based on the largest part of the heat flux intensity and the corresponding water temperature should be controlled with 1.5. Meanwhile, water velocity increased has little effect on the heat transfer capabilities.

Jan 1, 2015

By Jianxun Song, Hongmin Zhu, Qiuyu Wang, Jungang Hou, Shuqiang Jiao, Xiaobo Zhu

This work presents the results of a study on the Ti3+/Ti2+ couple redox potentials vs. Cl–/Cl2 at the temperature range (673 to 1073 K) in fused LiCl-KCl eutectic by direct potentiometric method. Initial concentrations of TiClx in solvents did not exceed 5.0 mol%. Basic thermodynamic properties of the reactions TiCl2+1/2Cl2(g)=TiCl3 were calculated using the temperature dependencies of apparent standard potentials of the couples E* Ti3+ /Ti2+.

Jan 1, 2014

By Martin B. Schranz

Copper sulfate pentahydrate is recovered from the spent etchant waste stream of a printed circuit board manufacturing facility by cooling crystallization. The fluidized bed crystallizer contains submerged cooling surfaces which are bathed in a stream of air. The air bubbles provide agitation which improve heat transfer, reduce fouling and maintain crystals in suspension. The recently patented apparatus (US 5,523,064) has advantages when compared to a conventional surface cooled crystallizer including capital cost, ease of operation and production of larger more uniform crystals

Jan 1, 1997

By Djona M. Gaballah I.

Selective chlorination of unroasted and roasted spent hydrorefming catalysts was studied between 300 and 600°C using the following gas mixtures : C12+CO, C12+N2 and CI2+air. Such materials contain Co, Ni and Mo compounds supported by alumina and/ or silica. They also contain variable amounts of V compounds, C, S, etc., accumulated during the life time of the catalyst. Direct oxychlorination of the C+S rich sample allows higher extraction rates than those obtained by the carbochlorination of the same roasted one. It seems that the roasting step doesn't favor the economic metals' recovery. Results of the chlorination of C+S poor spent catalysts, in the presence of CO, in the chlorinating gas mixture, or of carbon added to the sample, were comparable. Cobalt and nickel chlorides were .extracted from the chlorination residues by their dissolution with acidified water, whereas molybdenum and vanadium chlorinated compounds were recovered by selective condensation from the vapor phase. The recovery rates of valuable metals as well as the selectivity were higher for the chlorination of spent catalysts than results obtained by the hydrometallurgical processing of the same sample. Results of the scale-up of the oxychlorination of the unroasted sample confirmed those of the laboratory scale. The global recovery rates were about 88 pct of cobalt, 93 pct of molybdenum and 76 pct of vanadium. The carbochlorination was applied to the recovery of W and Ti from Denox catalyst that is a carbon and sulfur free one. Recovery rates higher than 99 pct at temperatures lower than 500 °C could be obtained. This may indicate that the chlorination process can be applied to the treatment of various industrial wastes or by-product containing transition and/or refractory metal compounds A flow - sheet for the pretreatment of these materials is proposed.

Jan 1, 1995

By H. Y. Sohn, S. PalDey

"A new chemical synthesis process for the preparation of intermetallic compounds has been developed. It involves the vapor-phase reduction of mixtures of constituent metal chlorides by magnesium vapor to produce intermetallic compounds in the form of fine powder. The advantages of the process include (a) the use of inexpensive raw materials, (b) low reaction temperatures, and (c) products in the form of fine particles. Titanium and nickel aluminides were prepared by this method. The effect of AlCl/TiCl3 partial pressure ratio on the formation of different titanium aluminides was studied. A two-phase mixture containing 80 mol % of TiAl and 20 mol % of TiA13 formed at an AlC13/TiC13 ratio of 10. The amount of TiA13 was maximized to 72 mol% at an AlC13/TiC13 ratio of 16. The maximum conversion of the limiting chloride TiCl3 was 94 % . In the case of nickel aluminides, NiAI, NiAl3, and Ni2Al3 were formed by reducing mixtures of NiC12 and A1Cl3 vapors. The effect of the partial pressure ratios AlCl3/NiC12 and Mg/NiC12 on the formation of nickel aluminides was studied. The maximum content of NiAl obtained was 98 mol % . At the AlC13/NiC12 ratio of 19, a two-phase mixture of 17 mol% of NiAl and 83 mol% of NiA13 was produced. The product particles were very fine in the size range of 0.05 to 0.2 µm.A. IntroductionIntermetallic compounds are attracting much attention [1]. Titanium and nickel aluminides have attracted a great deal of attention from the aerospace as well as automobile industries because of their potential for high-temperature application (e.g., low density, good oxidation resistance, and high-temperature strength retention [2, 3]). Gamma TiAl and two-phase (TiAl and Ti3Al) alloys [4] are used for gas turbine engine rotational components as well as automobile exhaust valves. TiAl3 is one of the most extensively investigated aluminum-rich intermetallics. Nickel aluminides are attractive because of their low densities, relatively high melting point and good high-temperature strength properties. For example, Ni3Al shows increasing rather than decreasing yield strength with increasing temperature [5]."

Jan 1, 1998

By M Phil Schwarz

"A CFD model for the gas-side of an impinging jet iron bath reactor has been developed to assist in the interpretation and design of oxidizing gas-melt reaction rate experiments. Heat transfer and reaction at the surface have been included. A free surface model, which solves for the liquid motion within the bath as well as the gas motion above the bath, has also been developed. This model also predicts extent and shape of the dimple formed on the liquid surface by the impinging jet. Both models have been run for conditions typical of jet impingement experiments using CO2 , H2O and O2• The main conclusions are• Results from the model for gas-side mass transport are in good agreement with the empirical correlation of Belton and Belton (1980)• Experimentally determined rates of decarburization by CO2 should be corrected for mass transfer because the experiments are often carried out under mixed rate control, eg for gas flow rate 10 L/min when the sulphur concentration is lower than 0.045• If the rate constant for oxygen reaction is greater than about 5 mol/m2.s.atm, it cannot be determined using a gas flow rate of 10 L/min or lower because of mass transfer control.• A cavity of depth 4.5 mm is predicted for a gas flow rate of 10 L/min and this substantially changes the flow field (and hence reaction rate) compared with a simulation in which the surface is assumed to be flat."

Jan 1, 1999

By Tao Li

The development of DP(Dual Phase) steels and TRIP(Transformation Induced Plasticity) steels has received much attention in recent years due to their high strength and simultaneous good ductility, which provides the potential for weight reduce and resource savings on certain components in automobile or other industries. So a controlled rolling process was simulated in the present study by thermomechanical simulator (Gleeble 1500) for producing DP steels on a kind of low carbon steel containing a small amount of Si and Cr. F+M dual phase microstructures have been obtained during continuous cooling processes of a wide cooling rate range from 10°C /s to 60°C /s. The grain size of the dual phase steel developed can be refined to less than 5 m through the mechanism of deformation induced ferrite (DIF) transformation. The ultrafine ferritic grains are equiaxed with high-angle boundary, and the martensite islands of an average size less than 5m disperse uniformly in the ferrite matrix. The ultrafine martensite islands not only inhibit the growth of ultrafine ferritic grains and improve the bonding of F/M interface, but also increase remarkably the strain hardening rate in the processing of the present Dual-Phase steel. As a result, the tensile strength of ultrafine grained Dual-Phase steel reaches higher than 1000 MPa. The result shows that an ultrafine grained Dual-Phase steel of low carbon and low alloy is promised to exhibit desired F+M microstructure by means of this new TMCP process.

Jan 1, 2006

By Mariola Saternus

The quality of the liquid metal has the biggest influence on the quality of the final products. In the metallurgical industry, and especially in aluminium production the refining process is the important technological stage. Today the most popular are refining reactors with impellers like URO ? 200, which can generate small gas bubbles. A rotary impeller also makes the metal bath to be stirred well. There are two basic hydrodynamic parameters: the flow rate of refining gas and the mixing of refining gas (impeller rotation) that influence metal stirring and generating small gas bubbles. The paper presents the influence of the flow rate of refining gas on the hydrogen removal process from aluminium (final hydrogen concentration), taking into consideration the refining process of AlSi7Mg alloy and using URO - 200. The mathematical model of this process is also presented. The equation needed for calculation of the final hydrogen concentration as a function of the equivalent bubble diameter is shown. Basing on this equation the calculations of bubble diameter and optimal refining time are done. This paper presents the physical model (the water one) of aluminium refining process and the gas dispersion taking into account the fact that the gas flow rate is changing from 2,5 to 17,5 l/min and the impeller speed is changing from 0 to 400 rpm. Schemes of gas dispersion in liquid metal in comparison with the model data are shown and the optimal values of the gas flow rate and the impeller speed are chosen.

Jan 1, 2006

By J. M. Skeaff

As much as 100% of the gold and 67% of the silver in a sulphur-bearing hydrometallurgical leach residue have been transferred to copper metal at copper smelting temperatures by dissolving the partially calcined residue in an iron-bearing slag maintained in equilibrium with the liquid copper metal and matte phases. The precious metals can then be recovered by conventional refining techniques. Copper can be recycled at least four times without any detrimental effects on gold and silver transfers and recoveries. Apparent copper recovery in the .process can be over 100% because of the copper content of the residue. Based on slag analys.es, the overal1 recovery of gold in the copper metal and matte phases varies from 94% to 100% under all conditions investigated. On the? same basis, silver recovery varies .from 9S% ?to 99% under optimum conditions, but is only 4S% to 73% under other, less attractive conditions. Unaccounted for silver losses of' about 30% make it difficult to determine the major factors affecting ?silver transfer and recovery. A method for implementing the technology on a commercial scale at a Canadian copper/zinc smelter has been proposed. A preliminary economic assessment and comparison of the proposed pyrometallurgical process with conventional cyanidation indicates that either process is economically attractive for recovering gold and silver from leach residues. Although the capital costs are higher, the pyrometallurgical process is simpler, has higher recoveries, lower operating costs and no .potential environmental problems related to cyanide disposal.

Jan 1, 1989

By Michael Stelter

Lead alloys are a typical material for anodes in technical electrowinning processes. The life time of those anodes differs from 2 years to more than 5 years in tankhouse practice depending on the type of alloy, the mechanical damaging and last but not least the chemical corrosion in the electrolyte. Different types of alloys, such as PbSb, PbCa, PbAg, PbSnCa or PbAgCa have been developed and used in the past, their rate of corrosion being more or less a philosophic discussion. Comparable investigations on the corrosion behavior in dependence of the concentrations of alloying metals, the grain structure and the mechanical and thermal treatment during production have not been conducted before. In the last years the Institute for Nonferrous Metallurgy and Purest Materials of the TU Bergakademie Freiberg investigated the corrosion behavior of the typical lead alloys for metal electrowinning under comparable conditions. Correlations between different alloys, mechanical treatments like rolling or thermal treatment like annealing to the rate of corrosion were made, leading to the conclusion that grain structure and grain size are of eminent importance for the rate of corrosion in technical electrolytes. From these results new and optimized lead alloy anodes can be produced with an increase in life time of the factor 3 ? 5. The optimized lifetime in terms of corrosion stability can not protect from mechanical damaging in tankhouse practice, but with a careful practice the increase in lifetime can save a lot of money and problems.

Jan 1, 2006

By E. R. Vance, D. R. M. Brew

"Historically, Ordinary Portland cement has been the preferred medium to immobilise arsenic. However, arsenic in cement gives rise to calcium-arsenic phases and their known decomposition to calcium carbonate and arsenic trioxide via atmospheric carbonation raises serious questions about the long-term suitability of cement for arsenic immobilisation. Alternative matrices such as low-temperature ceramics (LTCs) potentially offer superior resistance towards carbonation owing to the absence of calcium. Consequently, the potential for arsenic immobilisation using LTCs has been investigated. Both AsIII and AsV have been incorporated and samples assessed according to a standard leaching protocol. AsIII persists in the porewater of alkali-bonded LTCs as sodium arsenite rendering them unsuitable for immobilisation. Thermal treatment of these LTCs to consolidate the microstructure and reduce open porosity resulted in sodium-rich cryptocrystalline matrices that leached arsenic and sodium readily. The omission of sodium in acid-bonded LTC formulations resulted in leach data that were close to the target value of 5 µg/ml in Toxicity Characterisation Leaching Protocol tests.IntroductionArsenic is a carcinogenic substance and its adverse effects of on humans, flora and fauna have been well documented [1-5]. As a consequence, many papers have been written on the prospective handling of arsenic-bearing waste. These can largely be divided into: (a) cleanup of arsenic-contaminated water using bacteria, precipitation, and/or UV irradiation to generate arsenic-rich sludges for subsequent immobilisation; (b) cleanup of arsenic-contaminated soil via chemical extraction for immobilisation of the As concentrate; and (c) immobilisation of industrial waste contaminated with As."

Jan 1, 2008

By C. M. Acuña

At the Chuquicamata Division of Codelco-Chile high arsenic concentrates are produced, which at the smelter are processed via the Outokumpu Flash Furnace and Teniente Converters to obtain copper mattes. In the case of the Teniente Converters the production of matte grade near white metal composition is a common practice since the eighties and provided in the pyrometallurgical route no appropiate measures are taken, penalties have to be paid because of arsenic content in the anodes. During smelting huge volume of slag is produced and elimination of arsenic by slagging at this step is not economically attractive. Although during fire refining is possible to eliminate arsenic by use of mixtures of calcium and sodium carbonates this alternative is expensive, takes long process time and decreases the lifetime of the refractory lining. In spite of these facts a reasonably way to control arsenic in metal, and therefore in the anode, is taking, action in the converting step. The effects of oxygen and arsenic content in metal, arsenic in white metal and basicity index of the slag upon the distribution coefficient of arsenic between metal and slag were investigated at pilot and industrial levels. The best results are obtained for metals around 7,000 ppm oxygen and 0.3 basicity index slag, which results in a 5.7 distribution coefficient for a 5,800 - 7,100 ppm arsenic content in white metal, 18%-24% CaO slag at 1473 - 1523K. Furthermore, no significant/visible refractory wear has been realized.

Jan 1, 1999

By A. V. Tarasov

In the course of research aimed at improving the performance of the Vanyukov smelting process (VP) for treating sulfur raw materials in a pilot-scale furnace it has been found that an increase in the calcium oxide content up to 12% to 14% in case of smelting to produce high-grade matte results in a decrease in the copper content of slag by 0.05% to 0.3%. The residual copper content of slag can be computed by a formula taking into account an increase in the calcium oxide content of the feed material and that in the slag. In the course of research for improving the performance of the zinc-containing slag fuming process with blowing of the slag bath with combustion products of natural gas it has been found that the silica and calcium oxide contents have an effect on the degree of zinc sublimation. In case of slag containing 24.4% SiO₂ and 6.95% CaO by weight (SiO₂:CaO = 3.51), the residual zinc content of slag was 3.25%. The minimum residual zinc content of 1.95% was obtained in case of slag containing 22.5% SiO₂ and 14.5% CaO by weight (SiO₂:CaO = 1.55). An increase in the CaO content of slag up to 16% by weight with a ratio of SiO₂:CaO = 1.25 to 1.35 permits minimization of zinc losses in slag by achieving a residual zinc content of final slag in the order of 1%.

Jan 1, 2006

By William Petruk

The mineralogy of the primary and oxidized ores from the Malanjkhand porphyry copper deposit in India was studied to determine ore characteristics that affect metallurgy, and to assess applicable processes for recovering the copper. Three mineral assemblages were found. One occurs in primary ore, another in moderately oxidized ore, and a thir:d in intensely oxidized ore. Chalcopyrite, the main mineral in the primary ore, is relatively coarse-grained, with grain size increasing as the ore grade increases. High chalcopyrite liberations should be achieved at a relatively coarse grind, and good chalcopyrite recoveries should be obtained. The chalcopyrite, however, tarnishes readily and oXidizes to chalcocite in a relatively short time (several months). The presence of both the tarnished chalcopyrite and chalcocite may affect chalcopyrite flotation and reduce copper recoveries, The moderately oxidized ore occurs in an oxidized cap immediately above the primary ore, and stockpiled primary ore alters quickly to a moderately oxidized ore. Chalcocite is a major copper-bearing mineral in moderately OXidized ore. The concentrator processing this ore should be capable of handling a chalcocite-rich ore. The intensely OXidized ore contains a wide variety of acid-soluble copper-bearing minerals. Leaching may be required to recover the copper from them.

Jan 1, 1987

By Li Xi

This paper describes how a back-propagation neural network is built for predicting the properties of engineering materials from their other properties, compositions or processes. A predicted result of the impact toughness of a 12Cr-2Ni-1.5Mo stainless steel from its tempering temperature is presented. Furthermore, the combination of this neural network for prediction is able to supplement the unpredictability of the expert system outside its domain of expertise. An integrated system may perform more intelligently and solve more complex problems as well as human expert, in some case even better.

Jan 1, 1992

By George Kazonich

The high costs and environmental problems associated with making iron and steel in the United States is driving the development of new technologies to replace the blast furnace. A prototype reactor incorporating rocket technology was designed and built. This rapid rate reactor was operated successfully and consistently made iron metal. Minus 325-mesh magnetite particles could be reduced to iron metal in less than 50 ms in a high temperature flow through reactor. Iron product was recovered inside the reactor and in a downstream cyclonic separator. The results of typical operation and how parametric changes affected the reduction of iron ore concentrates are discussed.

Jan 1, 1993

By Pengfu Tan

In order to understand and control the formation of dioxins and furans in iron ore sinter plants and to possibly avoid expensive end-of-pipe removal stages, thermodynamic calculations on the stability of PCDD/Fs have been combined with sinter process modeling by means of kinetic simulations and computational fluid dynamics. Three thermodynamic databases of PCDD/Fs, derived using the Group Additivity approach and two computational molecular modeling methods, MNDO and PM3, respectively, combined with the SGTE database have been used to model the PCDDIF formation and the PCDD/F isomer distributions in iron ore sintering. The results show very similar conditions for the PCDD/F formation using the different databases. Concerning the isomer distributions of toxic PCDD/Fs, the calculated data derived from the MNDO method showed optimum agreement with measured values from industrial furnaces. The thermodynamic calculations also proved that the isomer distributions found in combustion processes are equilibrium values, while the concentration ratio of PCDDs and PCDFs in the wind boxes does not represent an equilibrium state. A CFD model of iron ore sintering was developed including the kinetics of 15 relevant chemical reactions with the aim of describing the temperature fields and the gas flow patterns in the sintering bed. On the basis of these information and experimental observations reported in the literature possible pathways for the PCDD/F formation in sinter plants have been identified: PCDD/Fs are formed in the critical temperature region of 250 to 450°C below the combustion zone, are then carried downwards with the gas and condensed close to the bottom of the sinter bed. Transported to the discharge end with the solid mixture, they are again released into the gas phase when the flame front approaches the bottom. PCDD/Fs are also formed in the last wind boxes when the hot off-gases cool down and reach the critical temperature range. Consequently, methods to reduce the dioxin formation reactions are proposed including inhibitor addition to the sinter feed and off-gas quenching.

Jan 1, 2003

By William Petruk, J. H. Gilles Laflamme, Jean Robitaille, Louis J. Cabri

"A quantitative mineralogical study using ore microscopy, electron microscopy, proton-microprobe, image analysis, and material balances was done on samples from the circuit of a concentrator in Quebec, with particular emphasis on the Cu concentrate. The ore contains many different minerals, of which the principal ones, in decreasing order of abundance, are pyrite, sphalerite, chalcopyrite, bornite, galena, tennantite, and pyrrhotite. Minor to trace amounts of covellite, chalcocite, stannoidite, mawsonite, colusite, wittichenite, miharaite, hessite, petzite, electrum, and an unidentified Cu-Pb-Bi-sulfide also occur.Liberation of pyrite is very high in all size fractions for all samples (ranging from 80-91 %). Liberation of chalcopyrite, bomite, sphalerite, and tennantite is relatively high, on average, in the head .sample and Cu concentrate (55-78% and 66-88%, respectively). Most of the chalcopyrite in the flotation tails is not liberated, whereas about one half of the tennantite and sphalerite are liberated in both the flotation and :final tails. Recoveries calculated for the Cu concentrate (on the basis of assays, mineralogy, and image analysis) are chalcopyrite 72. 5%, bornite 73. 7%, sphalerite 41.0%, tennantite 70.9 %, and galena (together with some trace minerals) 34.2%. It was also calculated that the Cu concentrate contains 10.0 % of the pyrrhotite and i.4 % of the pyrite.Materials balance calculations were done on the five major sulfide minerals to determine the mineralogical distribution of 13 major, minor, and trace elements (as determined by protonmicroprobe analyses). It was determined that tennantite is the principal carrier of Bi (67%), As (90%), and Te (86%) in the Cu concentrate. Therefore, removal oftennantite, which is mostly liberated in the Cu concentrate would significantly reduce these three contaminant elements, but at a loss of9% of the Cu, 2.0% of the Zn, and 0.7% of the Ag. The precious metals (Au, Ag) occur as discrete minerals (electrum, petzite, hessite). Some of the Ag also occurs in solid solution in bornite (23.1% of Ag in Cu concentrate), tennantite, and sphalerite. Four of the major sulfides (chalcopyrite, bomite, sphalerite, tennantite) in the ore also contain measurable concentrations of the following trace elements: Se, Cd, In, Sn, and Sb, occurring mostly as solid solutions. Some of these elements are also concentrated (up to about 18%) in minor and trace minerals such as colusite, stannoidite, and mawsonite."

Jan 1, 1999