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By John E. Dutrizac, Tzong T. Chen

"Laboratory experiments were undertaken to ascertain the behaviour of various ""impurity"" species during the precipitation of hematite directly from ferric sulphate solutions at 225°C and in the presence of 40 or 50 g/L of hematite seed. Copper, nickel and zinc are not significantly incorporated in hematite precipitates. Although the nickel contents increase to 0.22% as the Ni concentration increases to 60 g/L, the solid solution Ni contents are low relative to the bulk Ni contents. Thus, part of the Ni may be present as tiny particles of poorly soluble NiS04.H20. Increasing germanium concentrations to 2,000 mg/L result in products containing up to 0.59% Ge. The Ge occurs either in solid solution in the hematite or is adsorbed on the nanometer-size hematite crystallites. Increasing As(V) concentrations to 10 g/L increase the AsO4 contents of the products up to 16%. However, the products consist of hematite together with As04-containing Fe(SO4)(OH) and an unknown Fe-AsO4 species. All the hematite products contain - 1% SO4 which appears to be adsorbed on the nanometer-size hematite crystallites.IntroductionDissolved iron is a common impurity in most hydrometallurgical processing circuits and, generally, the iron must be eliminated prior to the subsequent recovery of the sought after metals. Simple neutralization of iron-rich solutions yields slurries which are difficult to thicken and filter. To address these concerns, the jarosite, goethite and hematite processes have been developed, and these technologies are able to reject the dissolved iron in a readily filterable form [1]. Despite its higher cost, the hematite process offers several potential advantages. Because hematite is an iron-rich, high-density compound, its formation would reduce the mass of residue and the size of a residue storage pond. Hematite is the thermodynamically stable form of iron under ambient conditions, and this stability would facilitate the impoundment of hematite precipitates. Furthermore, hematite has some market potential for cement manufacture and even for iron making [2]. In all the commercial hematite processes, the dissolved ferric ions are first reduced to the ferrous state. Subsequently, the pH of the solution is adjusted and the solution is then oxidized. The ferric ions gradually generated during solution oxidation hydrolyze and precipitate mostly as hematite, although commercial hematite products also contain trace or minor amounts of jarosite-type compounds. However, there are potential advantages in precipitating hematite directly from ferric ion solutions, as the reduction and subsequent oxidation of the iron are not required. Although the precipitation of hematite directly from relatively concentrated ferric sulphate solutions (up to 0.5 M Fe(SO4)is) was recently demonstrated [3], the behaviour of impurity species during hematite precipitation is largely unknown. To address this issue, systematic laboratory experiments were undertaken to ascertain the behaviour of a number of ""impurity"" species during the precipitation of hematite directly from ferric sulphate solutions at 225°C, and the results are presented in this paper."

Jan 1, 2012

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 Lee Fergusson

"The primary features of ViroMine™ Technology are introduced and applications of ViroMine™ Technology to mine site remediation and the treatment of a variety of intractable waste-streams, including a technical discussion of acid neutralizing capacity, metals binding capacity and longterm stability of results. Outcomes from four applications at high-profile international mine sites are presented: 1) the superfund site at the Gilt Edge Mine, South Dakota, USA (four years of data on the treatment of acidity, TDS and metals such as Al, Co, Fe, Mn and Zn); 2) one of Australia’s most polluted sites at King River Delta in Tasmania (treatment of TAA and TPA, and metal and metalloid contaminants such as As, Cr and Hg); 3) The Aljustrel “Aqua Forte” mine site in Portugal (high acidity, metal and metalloid contaminants such as Al, As, Cu and Zn) and 4) the Ulsan Iron Ore Mine at Ulsan, South Korea (treatment of metal and metalloid contaminants such as As, Cd and Ni).IntroductionThe commercialisation of ViroMine™ Technology has resolved some of the most intractable pollution issues associated with historic mining ventures on a global scale and has facilitated the neutralisation of Acid Rock Drainage (ARD), remediation of acidic and metal contaminated impoundments (including tailings dams) and promoted revegetation on tailings deposits and waste rock dumps. ViroMine™ Technology also enables current mining ventures to manage effluent simply and efficiently to meet increasingly stringent environmental standards and is enabling the mining sector to reconceptualise the management of mine spoil. The abilities of ViroMine™ reagents to neutralise the actual and potential acidity of sulphidic mine spoil coupled with the ability to bind metal and metalloid contaminants into non-bio-available forms are the key features delivering environmental and economic benefits to the mining sector and the broader community. Results from four projects utilising ViroMine™ Technology are presented to highlight the suitability of ViroMine™ Technology to treat all forms sulphidic mining wastes. 37"

Jan 1, 2008

By E. Yegan Erdem, Fiona M. Doyle, Alyssa A. Maich

"There is an expanding interest in synthesizing high quality magnetic nanoparticles, most notably for biomedical applications. Different processing routes have been reported for the synthesis of magnetite and maghemite. However, some ambiguity remains on their precise chemistry, intermediates, and final products, due to the structural similarity of maghemite and magnetite, and the relative ease of redox transitions during synthesis. Here we present the results of TEM, x-ray and electron diffraction, and SQUID studies aimed at characterizing the products from two different reaction systems, thereby clarifying the reaction chemistry. The first system hydrolyzed aqueous FeCh and FeCb chlorides with ammonia in a micro fluidic reactor at ambient temperature; although the reaction product displayed a uniform distribution, it included non-magnetic goethite and lepidocrocite. If the aqueous solutions contained dissolved oxygen, there appeared to be extensive oxidation of Fe(II). The second system thermally decomposed iron (III) acetylacetonate in ether. In prior studies, oleylamine has been reported to serve as both a reducing agent and capping ligand to control particle characteristics; however, our studies revealed little reduction, with maghemite dominating the reaction products.IntroductionMagnetite and maghemite nanoparticles are co=only used in ferrofluids, in medical applications, and in drug delivery. Superparamagnetic properties, along with low cytotoxicity, colloid stability and bioactive molecule conjugation capability, make these nanomagnets ideal for both in-vitro and in-vivo biomedical applications [1]. One of the major constraints on widespread adoption of nanoparticles for these applications is the amount needed. Typical batch synthesis methods produce polydispersed nanoparticles, which require further size selection procedures to isolate the mono disperse nanoparticle population needed for many applications. In order to maximize the yield of usable particles from a synthesis operation, the reaction conditions must be closely controlled. This requires full knowledge of how the reaction conditions control the various aspects of nanoparticle growth. Many methods have been used to synthesize iron oxides, including sonochemical reactions, mechanochemical synthesis, hydrolysis and thermal decomposition. This work examines the latter two methods, focusing on oxidation and reduction of iron."

Jan 1, 2012

By R. Upadhyaya

Aluminium alloy matrix cast composites have been synthesised by incorporating fine graphite powders (0.5 - 20 µm size) and chopped carbon fibres (6.5 pm P). 3-6 mm length) by liquid metallurgy technique. Incorporation of these second phase materials exceeding 6-8 wt% invariably resulted in agglomeration of the dispersoids and sometimes leading to even total rejection. It was found that small additions of mischmetal (1-3 wt%) during dispersion resulted in better incorporation without much agglomeration of the dispersoid as evident from the macro and micro structures of the composites. Further, the additions of mischmetal increased the volume of the effective incorporation of the dispersoid even to the extent 50- 60%. The mischmetal addition results in a significant increase in the power factor of the stirrer motor indicating an apparent increase in the viscosity of the system. The higher viscosity of the melt increase the shear transmission conditions within the melt during stirring thereby breaking the agglomerates of the dispersoids. The increased viscosity of the melt seems to be due to the formation rare earth - aluminium inter metallics precipitation, as observed in the metallographic studies, thereby making the process a "pseudorheocasting? technique. A provisional patent has been filed based on this work.

Jan 1, 1989

By Marco A. S. Aguiar, Luis G. S. Sobral, Vânia Mori, Paulo A. Medeiros da Silva

"Copper occurs in the crust of the earth, predominantly, as sulphides. Among the copper sulphide minerals, the chalcopyrite is the most abundant and the most refractory to the conventional oxidative processes. This work aims at developing an electrolytic process for treating a copper sulphides flotation concentrate, more precisely chalcopyrite (CuFeS2) and bornite (Cu5FeS4) in the percentages of 70 and 30%, respectively.This paper presents a low-cost operational electroleaching process for treating copper sulphides flotation concentrates, with a high chalcopyrite content. This research practical work aims at improving the copper extraction from that sulphide mineral, in a relatively short time with low-operating cost taking into consideration the influence of a cationic surfactant. The electrolyte of the electrolytic reaction system was a 2,0 mol.L-1 NaCl solution containing CTAB, a cationic surfactant. The electroleaching system contains one DSATM (dimensionally stable anode) anode and two nickel or copper foams (threedimension electrodes. During the electroleaching process the chloride ions are oxidized to chlorine at the anode surface, which in contact with the aqueous phase generate enough hypochlorite ions to oxidize chalcopyrite.The copper ions released from the chemical oxidation process are reduced at the cathode surface as metallic copper."

Jan 1, 2008

By Tracy Morris, Weldon Read, Luis Navarro

"Bismuth is a recognized contaminant in the electrolytic refining of copper that can render many cathodes to be outside ASTM standards and unsuitable for copper rod and other downstream products if not carefully controlled. This paper portrays the performance of Molecular Recognition Technology (MRT) for bismuth removal at the Amarillo Copper Refinery (ACR) and describes how the highly selectivity gel has been successfully used to achieve good bismuth removal and how many pit falls and draw backs have been overcome.IntroductionASARCO operates one of the largest copper refineries in the world at Amarillo, Texas. The main feed for this refinery is produced at the Hayden smelter in Arizona. During the operation of this smelter a variety of metals are carried as impurities in the copper anodes because of the diversity of concentrates and residue products used as raw materials in the smelter feed mix. Even though the impurities are concentrated enough to be detected at the smelter, it is difficult to remove them completely. A simple way to control impurities at the smelter is to minimize the addition of material with a high concentration of impurities to the charge in order to reduce the output of this metal species. All this leads us to have a ""refinery problem"" [1,2,3]."

Jan 1, 2012

By Paul Dewison

For nine years, from mid-1987 to mid-1996, the copper market enjoyed what appeared to be an endless boom in which prices were much higher relative to production costs than for most other base metals. After the boom ended abruptly mid-1997 with the Sumitomo affair, copper was burdened by an overhang of new projects that promised to swamp demand in what, with the Asian financial and economic crisis of 1997, had become a considerably worse consumption environment. Now, demand prospects do not look so bad. If, as we suspect, we will be dealing with a more rational market in the future, it becomes all the more important to forecast accurately the prospects for consumption. In this paper, we present a new methodology for copper demand forecasting. The methodology forms the backbone of the demand-side analysis for the multi-client study entitled "Long Tenn Outlook for Copper", co-authored by Metalica Ltd. and Bloomsbury Minerals Economics (BME). Key components of the methodology are as follows. (1) Relate demand to economic structure. (2) Focus on products rather than refined consumption. (3) Apply a consistent products/applications analysis to all countries and time series. (4) Incorporate scrap market dynamics within the analytical framework.

Jan 1, 1999

By José García-Antón, Valentín Pérez-Herranz, José Luís Guiñón, Henry Reyes

"The majority of chromium electroplating operations employ Cr(VI)-based baths. During these processes, Cr(VI) is reduced to Cr(III). Besides Cr(III) other undesirable impurities are present such as iron, copper and nickel. The build-up of the impurities limits the lifetime of the plating solutions. Since the disposal of spent chromic acid baths is expensive and can cause significant environmental degradation, there is increasing interest in finding ways to regenerate waste chromium liquors.In this work, an electrolytic cell separated by microporous ceramic diaphragms was used to regenerate chromium plating solutions. The effect of the ceramic diaphragm structure parameters, such as porosity and pore size, on the performance indicators of the electrochemical reactor (fractional conversion, current efficiency, product yield, specific energy consumption) was investigated.The fractional conversion, the product yield and the current efficiency increased and the specific energy consumption decreased with the decrease in porosity.IntroductionChromic acid is widely used in industrial applications such as steel manufacture, metal finishing industries, aluminium anodising, pasivation of cadmium, magnesium, and zinc, etching of plastics and another industrial operations related with processing ferrous and no ferrous metals [1]. These processes employ baths with high concentrations in chromic acid, about 180 and 350 g/L, where hexavalent chromium is reduced to Cr(III):"

Jan 1, 2008

By F. Guevara

The paper presents results of physical and turbulent three-dimensional numerical simulation of the gas flow in the wind box and reaction shaft of the concentrate burner of a flash furnace. Physical simulation work was carried out in a 1:5 linear scale model, where the velocity field was measured using a Pitot tube. The mathematical model consists of the three-dimensional averaged Navier-Stokes equations, turbulent kinetic energy and dissipation of turbulent kinetic energy using the Renormalization Group (RNG) theory for the k-e turbulence model. Computations were performed using FLUENT, based in a finite- volume code. The geometry of the concentrate burner was separated in two sections: wind box and reaction tower. Results obtained at the exit of the wind box were used as boundary conditions for the reaction shaft. The effect of boundary conditions on the numerical results was also studied. Results of physical and numerical simulations show an asymmetry of the velocity field at the exit of wind box. This asymmetry is possibly due to existence of a separated flow in the back of the exit ring. The agreement of physical and numerical results assess the capacity of the turbulence RNG k-e model to reproduce correctly the behaviour of the velocity field at the exit of the concentrate burner.

Jan 1, 1999

By Xiang Sun, Zheng Zhang, Jiann-Yang Hwang, Zhiwei Peng

"Nickel oxide nanoparticles were synthesized using sodium dodecyl sulfate as the surfactant and urea as the hydrolyzing agent and different calcination temperatures and time were selected for preparation. Nitrogen adsorption (BET), X-ray diffraction (XRD) and scanning electron microscope (SEM) were subsequently used to characterize the prepared samples. The effect of an external electric field on hydrogen adsorption over a prepared nickel oxide was carried out. The electric filed was introduced by a piezoelectric element, which is capable of autogenously generating charges under hydrogen pressure. Increased hydrogen adsorption was obtained from this study, which indicated a stronger interaction between the adsorbent surface and hydrogen.IntroductionMetal oxide has attracted great attention for adsorption because of their wide application in catalysis [1-7], gas storage [8,9] and sensors [10,11]. However, with respect to the usage in hydrogen adsorption, few research outcomes have been reported [12,13], since there remains the difficult task of synthesizing highly porous metal oxides with unsaturated metal centers, which account for the strong interaction with hydrogen [14,15]. Nickel oxides are polar materials with an intrinsic dipole moment. The external applied electric field could further enhance the dipole moment so that the hydrogen could be more strongly adsorbed."

Jan 1, 2012

By Cheng Gong-jin, Chu Man-sheng, Liu Zheng-gen, Zhang Yong, Liu Jian-xing, Xue Xiang-xin

"High chromium vanadium-titanium magnetite is one kind of Fe-V-Ti-Cr composite ore resources, which owes high utilization value. Owing to lacking systematic study on the sintering of this ore home and abroad, effects of carbon addition and basicity on sintering process and sinter metallurgical properties, such as sinter yield, vertical sintering speed, tumbler strength, sinter machine utilization coefficient, and low temperature reduction degradation were investigated systematically under laboratory conditions in the paper. The results shows that, when high chromium vanadium-titanium magnetite proportion is kept unchanged as 13% in sintering feeds, sintering process index and metallurgical properties are the optimum under carbon addition 5.0% and basicity 2.70, which meets the requirements of blast furnace burdens. This research provides technical parameters for practical sintering production of high chromium vanadium-titanium magnetite.IntroductionHigh chromium vanadium-titanium magnetite (hereinafter abbreviated as hi§h-Cr V-Ti magnetite), in which Fe is closely symbiotic with Ti and isomorphous with V and Cr1'- l, is one kind of typical vanadium-titanium magnetite resources with high comprehensive utilization value but the difficulties are extremely high due to complex chemical composition and mineral structure. At present, the feasible and mainstream utilization process of high-Cr V-Ti magnetite should be the route of agglomeration-blast furnace smelting. Thus, sintering production is the foundation for high-Cr V-Ti magnetite utilization. However, till now there are few research documentations on high-Cr V-Ti magnetite sintering home and abroad. Under the above background, this study focused on detailed researches of high-Cr V-Ti magnetite sintering. Sintering process uses the powders or fine iron ores to produce artificial rich ore with good metallurgical properties 4l Solid fuel provides 90% heat requirement during sintering15J. The appropriate amount of fuel and flux should be added during sintering in order to provide necessary heat and maintain the desired basicity16l. That is to say, carbon addition and basicity are two key factors affecting metallurgical properties of sintering products17J. Therefore, the effects of carbon addition and basicity on sintering process and metallurgical properties, including sinter yield, vertical sintering speed, tumbler strength, sinter machine utilization coefficient, and low temperature reduction degradation, are systemically investigated under laboratory conditions in the study, on purpose to achieve the optimization of sintering process for high-Cr V-Ti magnetite."

Jan 1, 2013

By Marco Pasetto

The possibility to re-use marginal materials (by-products) deriving from industrial activities in the construction of road infrastructures, as total or partial substitution of natural aggregates, successfully combines demands for economy and environmental sustainability. The paper presents the results of a laboratory study, conducted at the Experimental Road Laboratory of the University of Padova, to verify the suitability of a particular type of electric arc furnace slag to be recycled in the lithic skeleton of high-performance asphalt mixes (porous asphalt, high modulus mixes, stone mastic asphalt, nonskid surfacings) for road and airport flexible pavements. the process of transformation of iron and steel slag into a product that can be used in road building is described, along with the characterisation of the mixtures, plus an analysis of the results of a wide battery of mechanical-performance tests. This study forms part of wider theoretical ? experimental research being done at the University of Padova in order to improve knowledge of the characteristics of succedaneum materials and check their possible applications in road and airport construction.

Jan 1, 2006

By P. R. Khangaonkar

The variety of intermediates, middlings, complex materials and wastes produced in the conventional processing of tin ores as experienced in the tin industry in South East Asia is reviewed. The problems associated with the treatment of these materials so as to produce useful products by hydrometallurgical or pyro-cum-bydrometallurgical approaches are discussed. Results of treatment of amang middlings consisting of cassiterite, struverite, ilmenite, zircon, monazite etc by chlorination with carbon tetra chloride are presented. The efforts to leach tin without letting iron coming in, by alkali leaching of certain wastes of tin processing are also briefly indicated. It is felt that pyro-cum-hydrometallurgical approach can help a viable treatment of these materials so as to obtain usable or value added products.

Jan 1, 1994

By C. A. Morais

The present work describes the development of an efficient and relatively simple process to obtain high grade CeO2 from a mixed rare earth chloride solution. The process involves cerium oxidation and precipitation by addition of a KMnO4-NaCO3 solution. The experiments were carried out at room temperature (25 1° C). The results indicated that the major parameters affecting cerium recovery are the molar ratio of KMnO4/Ce, the initial acidity of the chloride feed solution and final pH of Ce(OH)4 precipitation. In strong acid solutions (pH < 1), the oxidation of Cl to Clo took place in addition to the oxidation of Ce(III) to Ce(IV), so increasing the permanganate consumption. Conversely, low acidity (pH >3) led to coprecipitation of the other rare earth elements. Under the selected conditions, cerium was selectively precipitated as ceric hydroxide, together with some manganese dioxide. Further purification was carried out by the dissolution of Ce(OH)4 in HCl, followed by precipitation as cerium carbonate. The filtrate was neutralised with a Na2CO3 solution in order to recover the associated rare earth elements for further separation. The final product, assaying 99.7 % CeO2, was obtained with a recovery of nearly 100%.

Jan 1, 2003

By John Hollow

The Fort Knox Mine is an open-pit operation, located in Alaska, which started commercial production in March 1997. A conventional Mill processes 38,000 tpd of a low grade (1.0 g/t Au) free milling gold ore with a low sulphide component (below 1%). Gold production (11% from gravity and 89% from cyanidation) exceeds 400,000 ounces per year. Short retention time (20h), low temperature (7oC) and low grade make high leaching kinetics critical for the performance of the process. In April 2001, the treatment of True North ore, which represented 14.4% of the mill throughput and contained more sulphide in the form of pyrite, arsenopyrite and stibnite, resulted in a substantial drop in the average gold extraction from 87% to 72.6%. Laboratory investigations indicated that the addition of lead nitrate increased gold extraction to 91.7%. Further investigations were initiated to determine the leaching parameters and the nature of the problem. Subsequently, a lead nitrate addition scheme was implemented at the Fort Knox Mill that resulted in 2002 gold production being in excess of 31,000 ounces higher than that estimated for the non-lead nitrate reagent scheme. This paper presents the results of laboratory investigations and modifications in plant operating practices.

Jan 1, 2003

By G. A. Brooks

The problem of treating concentrates with increasingly higher levels of arsenic and antimony is compounded by the trend to stricter environmental guidelines regarding the disposal of smelter wastes. Much of the arsenic and antimony from non-ferrous processes is recovered as oxide fume. The options for handling these fumes include recycling them to the smelter, stabilising and disposing of them, and recovering values from them. Whilst arsenic oxide has little value, there is a market for antimony oxide and this provides an incentive for devising techniques for separating antimony oxide from arsenic oxide before disposal of the arsenic oxide. Arsenic can be separated from antimony oxide by selectively volatilising the more volatile arsenic trioxide from a mixed oxide sample or by selectively condensing the less volatile antimony tetroxide at high temperatures, leaving arsenic trioxide to condense out at lower temperatures. The results of selective volatilisation experiments at 379 to 587 °C indicate that it is difficult to achieve an arsenic content below 5.0 wt.% using air or nitrogen as carrier gas due to the formation of solid solutions between the two oxides. Injection of oxygen into a mixed vapor stream improved separation by selective condensation and antimony tetroxide containing as low as 0.23 wt.% was obtained in laboratory experiments.

Jan 1, 1994

By E. O. Stensholt

The Hybinette electrorefining process for production of cathode nickel was in use at Falconbridge Nikkelverk A/S, Norway, until 1975 when conversion to the new chlorine leach process was started. In 1978 the conversion to electrowinning had been completed, but further major improvements to the process have been made up to 1987. After a major expansion program in 1985 - 87 the refinery has a nickel capacity of 54 000 mt Ni/year. The main feed materials to the process are converter matte from the Falconbridge smelter in Sudbury, Ontario, Canada, and from the BCL smelter in Selebi-Phikwe, Botswana. A typical composition of the mixed feed to the refinery is: 40 - 45% Ni, 25 - 30% Cu, 20 - 22% S, 2 - 3% Fe and 1.0 - 1.5% Co. The matte is chlorine-leached in the first process step, nickel being dissolved selectively in a train of leach-cementation tanks. Essentially all copper and sulphur that was present in matte appears in the leach residue as CuS. In 1986 an autoclave treatment stage was added to the process to improve nickel extraction from the leach residue. The resulting strong nickel chloride solution is purified by the process steps (1) precipitation of iron and arsenic, (2) solvent extraction of cobalt and other minor elements and (3) precipitation of lead and the remaining impurities. The nickel solution is then fed to the tankhouse, where various nickel products are produced by electrowinning. The chlorine gas that is produced during the electrolysis is returned directly to the chlorine leaching tanks to dissolve more matte. After stripping from the loaded organic phase and solution purification cobalt is also produced by electrowinning. The copper sulphide leach residue, which contains some nickel, is dead- roasted in fluidized-bed roasters. The sulphur is recovered and sold as sulphuric acid. The calcine is leached in spent copper electrolyte, from which cathode copper is produced by electrowinning. Precious metals and the remaining base metals are recovered from the copper leach residue. The Falconbridge chlorine process is very versatile. It can accept a wide range of impurities in the feed and still produce metals of exceptional purity.

Jan 1, 1988

By Matthias Schnitzler, Herbert Pfeifer, Ralf Bolling

"To transform metals high temperatures are usually needed. A fast and efficient heating can reduce the C02 emitted. The fastest way to heat metals is called direct flame impingement (DFI). The flame impinges upon the item being heated. For this method it is important to know the shape and length of the flame. Laser-induced fluorescence (LIF) technology allows measurements of a two-dimensional field without influencing the reaction or the flow. Commonly used is the measurement of OH-radicals, an indicator of the reaction zone.In the presented study measurements of a turbulent diffusion flame are shown. The position of the reaction zone and the influence of the distance between the item being heated and the burner are investigated. Conventional measurements and LIP-measurements are compared and the potential of DFI to increase the efficiency of heating metals is discussed.IntroductionDuring industrial heating processes a fast and efficient heating technology is required. Two important aspects are the NOx emission and the energy efficiency. The direct flame impingement (DFI) technology has the highest heat transfer rate possible with a gas/air flame. The turbulent high velocity flame jet impinges upon the item being is heated [ 1]. Due to the high heat transfer rate furnace and exhaust gas temperatures are lower. Therefore the energy efficiency is increased and the amount of NOx emitted is reduced.Hydroxyl- (OH-) radicals are an intermediate product that is generated during the combustion of hydrocarbons [2]. They are commonly considered as an indicator for the reaction zone and position of heat release. Figure 1 shows the hydroxyl-mole fraction in dependence of the distance along the gas flow. The figure clearly shows how fast the OH-concentration increases in the reaction zone. Figure 1 also shows that OH-radicals are present in the post combustion region, however in smaller concentration [3].The laser-induced fluorescence technology serves to measure the spatial distribution of OH-radicals in a two dimensional cross-section area of the flame. Therefore the flame dimensions and location can be determined with high spatial resolution without influencing the flow or the reaction [ 4,5]."

Jan 1, 2012

By Norberto Benitez, Christian Ludwig, Simona Regenspurg, Fabian Mendez

"Navarro is the main garbage dump in the city of Cali (Colombia). Operated since the late 1960s it collects about 1.600 tons of waste daily. The environment surrounding Navarro is highly contaminated and the pollutants released by the dump threaten human health in the adjoining neighborhoods. The goal of our project is to identify major pollutants released from the dump and their distribution in the surrounding ecosystem. In a first phase of the sampling and analysis program landfill leachate was collected and screened for heavy metals and for the most common persistent organic pollutants. This allowed us to identify the most relevant compounds on which we focused in a more detailed second phase investigation. These compounds were quantified in the vicinity of the landfill (groundwater, surface water, drinking water and soil) to get information on their mobility and possible pathways into the human body.IntroductionThe usual technique of waste disposal in most developing countries is by landfilling on not -, or not well controlled sites, where people live close by or even on the waste itself. A typical example for this practice is Navarro, the main garbage dump in the city of Cali (Colombia). Operated since the late 1960s it now consists of about 23 million tons of household and industrial waste. The dump is located on a wetland in the riverbed of the Cauca River, the main drinking water source for Cali. Two ponds of unknown permeability located next to the landfill collect a fraction of the waste leachate. During the rainy season, the ponds frequently overflow and drain into the soil (alluvial, loamy sediments) of surrounding sugar cane fields. The environment of Navarro is assumed to be highly polluted and there is evidence that it affects the health of nearby inhabitants. Specifically, the incidence of respiratory diseases was higher among vulnerable individuals (<3 and >50 years old) living in a <3 km perimeter of Navarro as compared with a control group (Solano et al., 2006). Further, a clustering of extremely rare congenital malformations (sirenomelias and cyclops) was observed in a small area during a short time period (<6 months) (Filigrana et al., 2008)."

Jan 1, 2008