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By Batric Pesic

The interactions of mineral-pyrite with T. ferrooxidans were studied by using a cyclic voltametry technique. The interactions with bacteria were examined during the entire growth stage of bacteria (fermentation), The pyrite ?surface invariably drastically changed ' its. properties at the second day of fermentation. Beyond two .. days of fermentation, the cyclic voltamograms were insensitive to convective diffusion produced by stirring. The product layer was examined by SEM,. X-ray diffraction and chemical analysis. The SEM study revealed that bacteria populated the pyrite surface at an extremely high density levels. The high density of bacteria, and the solid reaction products formed on the pyrite surface created conditions for pore diffusion which explained why the CVs became .insensitive to convective diffusion in solution (stirring). The x-r:ay diffraction study confirmed jarosite as a product layer. A mechanism of T. ferrooxidans cells serving as nucleation sites for jiarosite formation is proposed.

Jan 1, 1991

By James Douglas

A century ago the AIME meeting of 1899 was held at the Palace Hotel in San Francisco California in September. For his presidential address, James Douglas presented this paper which is reprinted in full with the kind permission of the AIME. It presents an interesting comparison relating to events and circumstances in the metallurgical industries at the close of last century. Being on the eve of a new century ourselves, the Editors of this volume of the COPPER 99-COBRE 99 Proceedings considered this paper would be of general interest, hence it is included here. Douglas believed in effective interchange of technical experiences and ideas. He considered the extreme secrecy surrounding the copper works at Swansea, Wales, the world center of copper only years before the time his paper was delivered, as one key reason for its decline, (and eventual closure of all copper plants there). In his paper, the pace of developments in various sectors such as transportation (railroads, the dominant means of I transportation at the time), the iron and steel and copper industries were examined, in much the same way as one might do but on the high technology of today. James Douglas was born in Quebec City, Quebec, Canada and spent his early life there. Forced to move to the United States for family and financial reasons, he went on to become a pioneer in the new Arizona copper industry, and with luck and good judgement with his interest in the new mining properties he also became very wealthy. Douglas was an accomplished mining and metallurgical engineer. He was the first President of Phelps Dodge and helped transform the small trading company of Anson Phelps and William Dodge into a mining giant.

Jan 1, 1999

By M. Jortikka

The smelting process of the old reverberatory furnace including its capacity has been improved over the years in different ways eg. with oxy-fuel burners, parallel reactors with the reverb or with various modifications of the reverb furnace itself. The future reverb modifications with old concepts are difficult or impossible as the increased copper losses in slag call for separate slag treatment and particularly the process modifications do not solve the environmental issues but instead mean unavoidable high capital and operating costs in gas cleaning and sulphur recovery. During the last decades improvement in process performance and increase in capacity of copper flash smelters has been achieved easily by substituting the pre-heated process air by highly oxygen enriched air. The flash furnaces of today, however, are inherently designed to operate with high oxygen enrichment. Further process improvement with a view to production costs and capacity increase as well as to the more stringent environmental requirements is possible with even higher oxygen enrichment. This, apart from the advantages it generates, requires improvements in and careful design of the feed system, concentrate burner, furnace cooling and the off-gas line as well as adaption of the flash converting instead of the conventional Peirce-Smith converters. A logical answer even for the revamping of the reverb smelters in the future is the total replacement of the reverb furnaces with flash smelting together with flash converting. This paper discusses the possibilities for future process improvements of the existing flash smelters taking into account the process concepts, equipment modifications and capital aspects not forgetting the environmental issues. The revamping of the PASAR smelter in Philippines is introduced as an example of a recent success story.

Jan 1, 1994

By James C. Sever

"With the advent of high energy costs and increasing concern for the environment leading to the incorporation the C02 life cycle as a criteria for the material used in a finished product, it is beneficial to analyze the plant and the process used in producing a raw material in order to identify practical, economic energy recovery opportunities. To this end a study was made of the proposed Nevada Clean Magnesium, Inc. Tami-Mosi reduction facility. Each source of waste heat is listed together with the assessment for potential co generation or direct recovery. The overall impact on energy requirement and C02 generation is provided.IntroductionHistorically metal reduction plants, large consumers of energy, do not recover waste heat. This occurred for many reasons:• Energy costs were low and the capital for a co-generation system could not be justified;• Waste heat sources contained entrained solids or liquids which would inhibit efficient energy recovery;• The exit temperature for the heat source was too low for efficient use by aaqueous Rankine cycle system.The business environment has now changed adding impetus to the recovery of energy previously discarded. Power costs have greatly increased. Global warming and the impact of carbon dioxide on the environment has become an issue which could impact the permitting of a plant. Technology improvements especially the development of a scaling environment waste heat boiler [l] and the development of the organic cycle Rankine cycle recovery system enable up to 70% energy recovery from ""low grade"" heat sources [2].With the inception of Nevada Clean Magnesium, Inc. 's (formerly Molycor Gold Corporation, Inc.)Northern Nevada Tami-Mosi project [3], an opportunity was presented to incorporate energy optimization from the initial design phase."

Jan 1, 2013

By Bruno Lebon, Koulis Pericleous, Georgi Djambazov, Mayur Patel

"High speed compressible jets are used in a number of steel-making applications. In the case of the BOF, a compressible oxygen jet reacts with a carbon-rich iron bath to reduce carbon levels and produce steel. The intensity of the process is governed by the speed of the jet and by the size and shape of the depression created in the metal and slag by the force of the jet, i.e. by the corresponding free surface. This is a difficult CFD problem, since there are compressible and incompressible regions in the flow domain, which need to be handled differently in a finite-volume (FV) pressure-correction scheme. Also, standard turbulence models do not account for compressibility, or the large difference in density between the cold oxygen jet and the hot reacting surroundings. Corrections are introduced to the k-E model to remedy this deficiency and the results are validated against experimental data. The compressible/incompressible boundary is handled through a transition region, based on Mach number.IntroductionThe deformation of a free surface by a compressible high speed jet is of paramount engineering interest, particularly for understanding the physical processes within a Basic Oxygen Furnace (BOF). In a BOF, a supersonic oxygen jet impinges on a molten iron surface, thereby creating a cavity. Oxygen penetrates the bath and removes carbon, resulting in low carbon steel [1].The challenges in modelling such a process lie in coupling a solution domain with distinct compressible and incompressible regions and in dealing with large density differences between the modelled gas and liquid. The modelling of compressibility within the jet is crucial, since the correct velocity profile in the jet is required to determine the cavity depth with accuracy."

Jan 1, 2012

By Tracy T. Morris, Luis G. Navaro

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

Jan 1, 2012

By Tapio Ahokainen

Commercial modeling software and increasingly efficient computers enable today computational fluid dynamics (CFD) to be used as a tool for a more comprehensive understanding of the flash smelting and flash converting processes. CFD modeling can be used for design purposes in many technological areas, but some relevant physical and chemical phenomena are still missing in the commercial CFD solver packages. Therefore, Outokumpu has developed several subroutines for solvers to describe analytically the phenomena in the flash smelting environment. CFD sub-models of the copper concentrate and matte combustion, the particle-particle-wall interactions and for more accurate radiation properties of the gas-particle suspension are needed to ensure reliability of numerical simulations on the flash smelting and converting vessels. Several basic combustion phenomena can be modeled with a number of commercial solver packages, but own models for combustion must be included in the case of sulfides as the feed. Mathematical models for copper concentrate and solid matte combustion have been developed during the last decade. They calculate compositions of the particles and temperature, based on extensive experimental research work in laboratory scale furnaces with validated kinetic parameters and temperature measurements of reacting particles. Inside and near the concentrate burner, the standard particle tracking methods do not include the particle-particle interactions and the particle-wall interaction is too much simplified to describe properly the particle collisions with the distribution cone. Therefore, additional models for the particle-particle as well as particle-wall interactions have been written and implemented. For thermal radiation, models for the emissivity of a gas mixture and for calculating the particle absorption and scattering coefficients have been developed and tested. In addition, the advanced radiation model can be used i.e. in the enhanced simulation of off-gas cooling in the heat recovery boiler area of the flash smelter.

Jan 1, 2006

By Akira Yazawa

The continuous converting has attractive advantages, but further experimental studies on the slag are required, when the process is considered thermodynamically. The summarized experimental results, obtained with iron silicate slag and with ferrite slag and results relating to actual operation are described and discussed in this paper. At first, equilibrium relations at controlled oxygen potentials among three melts of silica-saturated iron silicate slag, white metal and copper are investigated. The results obtained for slag agreed with the thermo-dynamical predictions. Namely, to suppress a magnetite separation, the system should be at high temperature; in the case of the S02 gas of 10 kPa, for example, magnetite did not separate from the slag at 1300°C, but at 1250 and 1200°C the slag was saturated with magnetite even at lower SO2 pressure. Copper losses caused by dissolution of its oxide increased with increasing 5O2 pressure, and were slightly lower than those reported in previous papers without the matte phase. When the continuous converting slag does not contain any appreciable amount of silica - in contrast to the conventional smelting slag ferrite slag would form, but there was no published fundamental work on-ferrite slags. Hence, the melting behavior and activities of the system CaO-Cu2O-Fe2O3 have been investigated. The liquidus diagram in nitrogen atmosphere was, constructed using both thermal analysis and quenching method. The low liquidus temperature region without magnetite separation was found in the part of low content of Cu2O in the section Cu2O-CaO-Fe2O3 and Cu2O?Fe2O3¬CaO?Fe2O3. The activity of Cu2O in the system was also measured. Slags, composed-of CaO, Cu2O and Fe2O3, in platinum crucibles were equilibrated at 1250°C and controlled oxygen pressures. After quenching, the-composition of slag and platinum crucible were determined qualitatively. On the thermo-dynamic analysis of the results, iso-activity lines were drawn, and it was shown that the slag in the converting furnace of the Mitsubishi process exists in an adequate region of the composition triangle.

Jan 1, 1976

By J. D. Sunderkötter, M. F. Stroosnijder, V. A. C. Haanappel

"TiAI-based intermetallic compounds have attracted considerable interest as structural materials for high-temperature applications due to their low density and substantial mechanical strength at high temperatures. However, one major drawback hindering industrial application arises from the insufficient oxidation resistance at temperatures beyond 700 °C. In the present contribution some general aspects of high temperature oxidation of TiAI-based intermetallics will be presented. This will be followed by a discussion of the influence of alloying elements, in particular niobium, and of the effect of nitrogen in the oxidizing environment on the high temperature oxidation behaviour of such materials.Extended AbstractIntroductionTiAI-based intermetallics are being considered as construction materials for high temperature components, e.g. in aircraft and car engines, due to their low density and substantial mechanical strength at high temperatures, see e.g. [1,2]. The best ductility can be attained with alloys consisting of y-TiAI with around 5-15 vol.% Q2-Ti3AI. However, one major hindrance to industrial application arises from the insufficient oxidation resistance at temperatures beyond 700 aG. In spite of their high aluminium content, TiAI-based intermetallics do not generally form long-lasting protective alumina scales. After longer exposure times the scales, which are initially rich in alumina, deteriorate and scales consisting of mixed alumina and titania predominate, with high growth rates similar to pure titania.It is not the intention of the present paper to present a general overview of the high temperature oxidation behaviour of TiAI based intermetallics, for which the reader is referred to the literature [3,4]. In the present contribution some general aspects of high temperature oxidation of TiAI-based intermetallics will be presented. This will be followed by a discussion of the influence of alloying elements, in particular niobium. The effect of nitrogen in the oxidizing environment on the high temperature oxidation behaviour of these intermetallics will also be considered."

Jan 1, 1996

By T. T. Chen

Secondary copper anodes are generally rich in Sn, Pb, Ni and Sb, but are notably deficient in Se, Te and Ag. In the secondary copper anodes, most of the Ni, virtually all of the Ag, slightly more than one-fifth of the Pb, about one-third of the As and Sb, and approximately one-tenth of the Sn are in solid solution in the copper. The remaining impurity contents occur as 1-5 µm grain-boundary inclusions in the anodes, and these are mainly Cu2O, SnO2, Cu-Pb-As-Sb-Bi oxide, Pb-Sb oxide, Sn-Ni-Zn oxide, Cu-Sn-Ni oxide, Cu-Sb-Ni oxide (Kupferglimmer) and trace Cu2(Se,Te). Barium sulphate, which originates from the mold wash used in casting, is also present in the anodes. During electrorefining, the BaSO4, SnO2, Pb-Sb oxide, Sn-Ni-Zn oxide, Cu-Sn-Ni oxide and Cu- Sb-Ni oxide inclusions are liberated and accumulate in the slimes layer. Solid solution Ni dissolves and the Ni accumulates in the electrolyte. Solid solution Sn and Pb dissolve, but partly reprecipitate as Sn arsenate and PbSO4, respectively. Solid solution Ag dissolves but rapidly reacts to form Ag2(Se,Te), Ag powder, Ag-bearing Cu2O, (Cu,Ag)SO4 or a complex oxidate phase. Partial dissolution of the Cu-Pb-As-Sb-Bi oxide particles takes place; the Pb component is converted to PbSO4, whereas Cu, As, Sb and Bi dissolve. The reacted particles retain the morphology of the original Cu-Pb-As- Sb-Bi oxide phase. Some of the solubilized As, Sb and Bi remains in solution, but much reprecipitates as SbAsO4, As-Sb-Bi oxide, and as a poorly defined oxidate phase which consists mostly of Cu-Ag-Pb arsenate-sulphate. The high Sn contents of secondary copper anodes do not seem to affect the behaviour of the anodes during electrorefining.

Jan 1, 1999

By Lijun Liu, Yingwei Li, Jianhua Liu, Jinhui Peng

"As essential equipment in the metallurgical industry, current air heat exchangers cannot meet the requirements of high temperature heat transfer. In this paper, an energy efficient air heat exchanger, based on accumulation of the heat generated by microwave absorbing materials, is presented according to heat transfer theory and principles of the microwave field. A tubular shaped heat exchanger was designed and built up through temperature-rising curve, and experimental research of microwave high-temperature air heat exchangers was carried out. It was found from experiments that the tubular shaped heat exchanger fabricated using material B could be used for high temperature heat transfer system, and equilibrium temperatures could reach up to 457—485?.IntroductionHeating or cooling of air by heat exchangers is commonly practiced in a wide range of industries including construction, chemical, machinery, textile, printing, and dyeing [1-3]. Generally such heating or cooling of air is achieved in pipe heat exchangers. There are several drawbacks for such heat exchangers, namely, (i) the limitation of temperature to which the pipes can be heated, (ii) tendency to oxidize at high temperature, and (iii) poor strength of metallic pipes at high temperature. These limitations do not allow pipe heat exchangers to be operated at high temperatures [4-6].Microwave heating of inert solids, which are stable at high temperature, is a possible solution to achieve high temperature of the medium in air heat exchangers. It is well-known that microwave heating is an efficient, clean, safe, easy-to-control heating method. Microwave heating utilizes the dielectric and magnetic properties of a material. When microwaves penetrate and spread into the dielectric material, electrons, ions, etc move in the internal electromagnetic field, while the elasticity of inertia and friction impede these movements. This results in a significant thermal effect, increasing the surface temperature rapidly [7-8]. This paper studies mainly design and experimental research of microwave high-temperature air heat exchanger."

Jan 1, 2011

By Ragnhild E. Aune, Shahid Akhtar, Reza Beheshti

"The potential use of Black Dross (BD) as a raw material for the production of refractories, fluxing agents and glasses is the main motivation of the present study. Heat treatment experiments were carried out in Ar, and under reduced pressure (20 Pa), to evaluate the salt removal efficiency. The chemical composition of the BD after heat treatment was investigated by SEM-EDS and XRD analyses. Based on the present results, it is established that the salt starts to evaporate at ˜1273 K in Ar, and under reduced pressure. The salt removal efficiency in a 20 g sample was found to increase in both cases as a function of time and temperature. Moreover, in Ar the chlorine concentration was lowered to 0.3 wt% after heat treatment at 1523 K for 10 hours. Under reduced pressure, however, 0.2 wt% residual chlorine was obtained after 8 hours at 1473 K.IntroductionIt is believed that aluminum recycling in the near future will become the main route of aluminum production [1]. Black dross (BD) that is produced during this process contains, among other things, high amount of salts like NaCl and KCl [2, 3]. Almost 800,000 tons of BD is annually land filled in United States and this number continues to grow with the increase in aluminum recycling [2]. The BD should be dumped in controlled land field and it is costly procedure [4, 5].The water-soluble compounds in BD react with water or environmental humidity and release chlorides into the water and/or generate toxic gases such as H2, CH4, NH3 and H2 S [6-8]. In the Europe, BD is considered as toxic waste and its disposal as landfill is forbidden [8, 9]. After salt removal, the BD is considered to be non-hazardous and can be buried under ground [10].On the other hand, BD do also contains many relatively valuable compounds that may be changed in to useful materials as a result of further treatment [11, 12]"

Jan 1, 2012

By D. McConchie

Management of caustic red mud wastes at the QAL bauxite refinery uses an innovative approach . involving neutralising the red mud with seawater; solids settle in a Red Mud Dam and residual water (pH = 8.6) is discharged to a tidal inlet. A survey of 18 trace elements in sediment, water, mangroves and molluscs, and an ecological survey of benthic fauna in the inlet, and at near-pristine control sites, revealed no significant trends that were linked to the discharge, except for the concentration of Al which was slightly elevated within 100m of the outfall. Trace element concentrations in water samples were close to, or below, world average seawater values and oysters collected near the outfall were acceptable for human consumption. The impact of discharges is minimised by a high tidal range, >60% flushing of the inlet in each tidal cycle, and the very high trace element binding capacity of sediment in the dam (> 100meq/ 100g dry mud).

Jan 1, 1996

By Qingyu Deng, Shiwei Ma, Guibao Qiu, Hua Wang

"The flow behavior of the blast furnace slag bearing titanium, like viscosity, play an importance role during the iron-making process with the vanadium-titanium magnetite, which is a very special minerals in Panzhihua, China. The dependency of the viscosity on the chemical composition like TiO2, Al2O3, MgO, binary basicity (CaO/SiO2), temperature, reaction time were studied. The experiments showed that the viscosity decreased with the increase of TiO2, MgO content and binary basicity, and it increased with the increase of Al2O3 content and temperature. The viscosity showed a slight decrease within 60mins’ reaction with graphite crucible, however, it increased rapidly afterwards with the formation of Ti(C, N).IntroductionThe ordinary iron ore has been an essential part of raw materials for vanadium-titanium magnetite smelting in Panzhihua to avoid a series of problems, such as slag thickening, adhesive bond of slag and hot metal, etc. The ratio of vanadium-titanium magnetite has been decreased gradually since 1970s, and has down to about 65% now. However, with the substantial appreciation of price of imported ordinary iron ore, Panzhihua Iron and Steel Group aims to increase the ratio of vanadium-titanium magnetite and decrease the dependence on ordinary iron ore in order to lower the cost of smelting process."

Jan 1, 2012

By Dao Su, Ganghua Fu, Xuling Chen, Yufeng Guo, Min Gan, Tao Jiang, Xiaohui Fan

"The sinter quantity and quality of limonite in the magnetite and hematite sintering models were studied and compared. For the sintering of magnetite, the results showed that the increase of limonite improved the permeability of sinter mixture, increased the sinter quantity and quality. The sinter strength and productivity were decreased when the proportion of limonite exceeded 50%. The appropriate proportion of limonite was 40%-50%. For the sintering of hematite, the sinter quantity and quality were first maintained at the same level thereafter declined, more obviously when the proportion of limonite exceeded 40%. The amount of calcium ferrite increased whose shape changed from acicular to leaflike and block gradually with the proportion of limonite increased from 0% to 80%.IntroductionWith the fierce competition of domestic and overseas iron markets in the twenty-first century, cheap ores such as limonite are used to be sintering raw materials to cut the costs of sinter and pig iron for steel making, and boosts the competitiveness of steel companies [1, 2]. In addition, as the reserve volume of hematite of high grade is reducing year by year, the usage amount of limonite in sintering are expanding in major domestic and international sintering plant [3, 4]. Sintering can be divided into two types, majoring in concentrates and fine ores, according to the different types of raw materials. The sintering characteristics of limonite in the two types above have been studied and compared in this paper, which makes a significant sense for the research of limonite sintering properties and guidance of ore proportioning in sintering plants."

Jan 1, 2012

By M. J. Adam

The U.S. Bureau of Mines is investigating the partitioning of selected complex minerals into simple phases using sulfidation reactions. Successful partitioning of complex mineralogy to simple phases may afford an opportunity to improve selective extraction of mineral constituents of economic value. The research has shown that complex minerals, such as chalcopyrite (CuFeS2) and pentlandite [(Fe,Ni)9Se]' may be partitioned to the simpler phases covellite (CuS) plus pyrite (FeS2) and vaesite (NiS2) plus pyrite (FeS2), respectively. Demonstrations of these reactions were verified through long-react ion-time (24 h or more) experiments, but basic rate investigations and modeling were not included in the previous research. This report describes research aimed at determining the rate at which the complex mineral CuFeS2 converts to the simple sulfides CuS plus FeS2. Small samples of CuFeS2 were blended with elemental S prior to thermal treating under an He atmosphere for time periods up to 4 h. Products from each treatment period were characterized using metallography, chemical analysis, X-ray diffraction (XRD), and scanning electron microscopy (SEM). Results of the investigation revealed a rapid conversion of CuFeS2 to CuS plus FeS2 early in thermal treatment periods. As the reaction occurred, a CuS rimming of particles was observed which separated the reacting species (CuFeS2 and S) and caused a considerable decrease in transformation rate.

Jan 1, 1991

By N. M. Komkov

The main operation of obtaining zinc from sulfide raw materials by hydrometallurgical technologies is the oxidation roasting of zinc concentrates in fluidized bed furnaces. The technical-economic parameters are determined by the parameters of the roasting process, which depend on the composition of the initial raw materials, the temperature of the bed and on other factors. The predetermined roasting temperature is maintained due to the change of specific efficiency as well as to the quantity of the heat removed from the bed. The efficiency of caissons depends at a high degree on the composition and the thickness of the accretion formed on the surface of the caissons. Forecasting the roasting results is impossible unless we know the mechanism of the accretion formation. The aim of the present paper is the thermodynamic analyses of the behavior of the charge compositions under roasting and the determination of the potential mechanism of the accretion formation. The thermodynamic analyses show that under conditions of the oxidation roasting the thermodynamic probability of the formation of zinc sulfate is higher than the probability of the oxide formation until a temperature of873 OK is reached. The thermodynamic probability of the formation of the lead sulfate is higher than the probability of oxide formation in the entire temperature range of roasting. The probability of formation of ferrites and silicates of zinc decreases only insignificantly the sulfate stability. The results of the investigation of the accretions composItion formed under roasting of concentrates with particle sizes less than 0.02 J..lm (60%), containing 65% of sphalerite (ZnS), 12% of pyrite and chalcopyrite (FeS2 and CufeSz) each, 3% of galenite (PbS), 7% of silica and other non-ore minerals, have shown that the composition of accretion varies depending on the depth of the accretion layer. The accretions on the caissons and the thermo-siphons consist mostly of zinc sulfate (more than 50%). The accretions of forehamber consist mostly of zinc oxide. They also contain ferrites and silicates. The formation of the sulfate zinc accretion in the cold parts of the fluidized bed furnace (the caissons and thermo-siphons) may be explained by a lower temperature on the surface and probably by a catalytic influence of the present oxides in the formation of S02 and sulfates. The nature of the structure of the accretion in the hotter parts of the furnace may supposedly be explained by the formation of elemental vaporous zinc during roasting.

Jan 1, 2003

By Christopher B. Vierrether

Reflected light microscopy, scanning electron microscopy, and electron microprobe analysis have been used to determine the mineralogy, phase percentages, grain sizes, textures, and partitioning of cobalt and nickel in two cobalt-nickel rich mattes. These mattes were prepared by submerged bath smelting from a flotation cobalt-nickel concentrate containing 4.8% cobalt and 5.1% nickel. The concentrate was derived from lead-zinc-copper ores of the Viburnum Trend, southeast Missouri. Eleven discrete phases have been distinguished in the matte samples, three of which contain significant cobalt and nickel. The phases are cobaltpentlandite ((Co,Ni,Fe)9S8), cobalt-bearing marmatite ((Co,Fe,Zn)S), shandite (Ni3Pb2S2), bornite (Cu5FeS4), galena (PbS), magnetite (Fe3O4), pyrrhotite ((Co,Ni,Cu,Fe)1_xS), chalcocite (Cu2S), CuPbS phase, metallic copper, and metallic silver. Cobaltpentlandite and cobalt-bearing marmatite- occur in coarse grains (50 µm) that would separate readily during grinding, but shandite contains small (5 - 10um), abundant inclusions of pyrrhotite and bornite.. Some mineralogical variations between the two matte samples were due to differing degrees of oxidation during smelting,

Jan 1, 1988

By N. M. Komkov

The main operation of obtaining zinc from sulfide raw materials by hydrometallurgical technologies is the oxidation roasting of zinc concentrates in fluidized bed furnaces. The technical-economic parameters are determined by the parameters of the roasting process, which depend on the composition of the initial raw materials, the temperature of the bed and on other factors. The predetermined roasting temperature is maintained due to the change of specific efficiency as well as to the quantity of the heat removed from the bed. The efficiency of caissons depends at a high degree on the composition and the thickness of the accretion formed on the surface of the caissons. Forecasting the roasting results is impossible unless we know the mechanism of the accretion formation. The aim of the present paper is the thermodynamic analyses of the behavior of the charge compositions under roasting and the determination of the potential mechanism of the accretion formation. The thermodynamic analyses show that under conditions of the oxidation roasting the thermodynamic probability of the formation of zinc sulfate is higher than the probability of the oxide formation until a temperature of 873°K is reached. The thermodynamic probability of the formation of the lead sulfate is higher than the probability of oxide formation in the entire temperature range of roasting. The probability of formation of ferrites and silicates of zinc decreases only insignificantly the sulfate stability. The results of the investigation of the accretions composition formed under roasting of concentrates with particle sizes less than 0.02 um (60%), containing 65% of sphalerite (ZnS), 12% of pyrite and chalcopyrite (FeS2 and CuFeSz2 each, 3% of galenite (PbS), 7% of silica and other non-ore minerals, have shown that the composition of accretion varies depending on the depth of the accretion layer. The accretions on the caissons and the thermo-siphons consist mostly of zinc sulfate (more than 50%). The accretions of forchamber consist mostly of zinc oxide. They also contain ferrites and silicates. The formation of the sulfate zinc accretion in the cold parts of the fluidized bed furnace (the caissons and thermo-siphons) may be explained by a lower temperature on the surface and probably by a catalytic influence of the present oxides in the formation of S02 and sulfates. The nature of the structure of the accretion in the hotter parts of the furnace may supposedly be explained by the formation of elemental vaporous zinc during roasting.

Jan 1, 2003

By W. Petruk

The behaviour of galena, chalcopyrite and tetrahedrite during floration of a fine-grained base metal ore from New Brunswick was investigated by image analysis study of the mill concentrates and tailings. The minerals were analyzed to determine the grades and recoveries as related to free and unliberated mineral grains and their size distributions. The results show that only 37 wt % of the galena was liberated but 88 wt % of the free galena was recovered, indicating good mill performance for the lead. The lead recovery was 65 wt %, with the main loss due to unliberated galena. Most of the unliberated galena lost to mill tailings is so fine-grained that galena liberation and Pb recovery would not improve significantly by re-grinding. Chalcopyrite liberation was 56 wt % but only 75 wt % of the free chalcopyrite was recovered. Copper recovery was 45 wt %, with the chalco-pyrite loss in the mill tailings being both as large free grains, and as small and large unliberated grains. It was calculated that copper recoveries could be improved about 8 to 10 wt % by changing the concentrator operations and by regrinding. Concentrator operations hive already been modified and copper recoveries have improved about 5 wt %. About 29 wt % of the silver was lost to tailings mainly as both free and unliberated, large and very small, Silver-bearing tetrahedrite grains. It was calculated that about 25 wt % of the silver in the tailings might be recovered by improved milling conditions and by regrinding.

Jan 1, 1981