Search Documents

By J. E. Dutrizac

A mineralogical study of a weak acid leach residue from the Clarksville zinc plant of Savage Zinc Inc. was carried out. The study focused on Pb and Cd as these elements most significantly impact on the environmentally acceptable disposal of the residue. The residue consists of major amounts of bassanite, zinc ferrite and various Zn-Pb-Fe-Cd silicate species. Also present are lesser quantities of PbSO4, sphalerite, Fe2O3 quartz, Mn-Pb-Fe oxides, SrS04, (Pb,Sr)SO4 iron gel-silica gel, jarosite and Ti oxide. The principal Cd carriers are the zinc ferrite, which contains up to 9.00% Cd and likely accounts for -45% of the total Cd content of the residue, and the various silicate species which contain up to 6.97% Cd and account for about 45 % of the total Cd. The sphalerite is a minor Cd carrier containing an average of 0.35 % Cd and accounting for -5 % of the total Cd; the other carriers contribute only trace amounts to the total Cd content. The major Pb carriers are PbS04, Pb-bearing silicates and Mn-Pb-Fe oxides. Minor proportions of the total 1.09% Pb content of the residue are carried by SrS04 and (pb,Sr)S04' Trace Ph carriers include the iron gel-silica gel, Fe-Zn-AI oxide and bassanite. The residue after the toxicity characteristic leaching procedure (TCLP) is mineralogically very similar to the initial weak acid leach residue; the amounts of calcium sulphate are approximately the same in the two products. The principal Cd and Pb carriers are also the same as those noted in the initial residue, except that some dissolution and reprecipitation of Pb-Sr sulphate takes place. That the residue fails the TCLP test is likely a consequence of the superficial dissolution of Pb and Cd from species such as PbS04 or Zn-Pb-Fe-Cd silicate.

Jan 1, 1995

By Steven Wright

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

Jan 1, 2006

By Toshiki Kabutomori

In fuel cell powered automobiles, hydrogen is required to be stored in materials that have a hydrogen storage density of over 4 mass%; further, these materials should be capable of supplying hydrogen by using the waste heat from a fuel cell, which is at a temperature of 373 K, in order to match the mileage of gasoline-powered vehicles. A Ti-Cr-V alloy, which exhibits a BCC structure and forms a solid solution, is a promising candidate for onboard hydrogen storage materials. Although it has a large hydrogen storage capacity of over 3.9 mass%, the rechargeable hydrogen capacity is limited to approximately 2.6 mass%. In this study, the effects of fine pulverization of the alloy on PCT (hydrogen pressure-composition-isotherm) characteristics were investigated in order to improve the rechargeable hydrogen storage capacity of the alloy. From the PCT measurements of the finely pulverized samples of the alloy, a plateau in the absorption curve was observed to begin at a hydrogen concentration of 0.5 mass%; further, a rechargeable hydrogen storage capacity of 3.3 mass% was obtained. This was greater than that obtained from the sample that was not finely pulverized, i.e., 2.5 mass%. However, the plateau width in the desorption curve was 2.5 mass%, which was the same as that observed for the sample that was not finely pulverized. The increase in the rechargeable hydrogen capacity during absorption is attributed to the precipitation of the -hydride phase (MH~2) directly from the metal phase (phase). The precipitation of the phase (MH~0.5), which should be formed in low hydrogen concentrations, is suppressed as a result of a possible reduction in the internal defects such as dislocations, vacancies, and grain boundaries by fine pulverization and annealing of the alloy.

Jan 1, 2006

By Qingsheng Liu

A new method of recycling aluminum dross for preparation Al-Si-Ti alloy was studied in this paper. This was carried out in two processes. first the aluminum doss was pretreated by leaching and calcining process, the fine purity and phase of the intermediate oxide powder up to electrolysis demands, then, could be obtained when aluminum dross after washing have been leached for 2h at 100? in 20% hydrochloric acid and calcined for 2h at 1200?, which was treated by cryoite-based molten salt electrolysis. Finally, the Al-Si-Ti alloy was successfully obtained through electrochemical co-deposition in the cathode shows a typical as-cast microstructure. This new recycling method can produce high quality alloy and may bring remarkable economic and social benefits.

Jan 1, 2010

By Chai Liyuan

Chromium-containing slag was detoxified by the method of microbial treatment using Ch-1bacteria isolated from nature by our research group, belonging to achromobacter sp. and with the characteristic of reducing high concentration of Cr(VI) in alkaline solution. The detoxifying process of Ch-1 to chromium-containing slag was studied by column-leaching techniques respectively. The results indicate that Cr(VI) in leachate can not be detected when chromium-containing slag has been column-leached for 7 days, and Cr(OH)3 content in precipitate is up to 32.8% with great value of resource recycling. Flowchart of engineering experimentation was ascertained based on the parameters of column-leaching experiments. Using the technique of pelletization of chromium-containing slag heap-leaching by Ch-1,the leaching rate of water-soluble Cr(VI) existing in chromium-containing slag reaches up to 100%, while the leaching rate of full chromium is up to 90%, when the process has been operated for 7-10 days under the conditions of 25-40C and consecutive spray by circular leachate. The content of Cr(VI) in chromium-containing slag after detoxified meet the national identification standard for extraction procedure inxicity for hazardous wastes(GB5085-1996) in China, moreover approximately 90% of Cr(VI) existing in chromium-containing slag has been recycled.

Jan 1, 2006

By Rauf Hurman Eric

In this review paper the effect of composition and temperature on electrical conductivity and viscosity of the slags encountered in electric smelting of PGM-containing sulfide concentrates is described along with their liquidus temperatures. Optimization of slag composition is attempted on the basis of opposite trends of viscosity and electrical conductivity. Metal losses to slag, matte-slag separation and matte settling are also discussed in conjunction with interfacial and surface tension concepts. The electrode immersed in the slag phase is the main factor in the design and operation of the furnace. The most important electrode parameters are the size and the positioning in the slag phase which are determined by the slag resistivity, furnace resistance, cell constant and power input. The flow of heat generated by the electrode current determines the energy distribution and furnace dimensions creating viscosity profiles within the slag phase which in turn affects the flow conditions. Thus the flow of slag is discussed together with furnace geometry, stirring action, buoyancy and electromagnetic effects and the action of the electric furnace as a settler is emphasized. A discussion on the design d production capacity of the furnace is provided which are based on considerations derived mainly from slag properties.

Jan 1, 2006

By Matthew Jeffrey

Due to the increasing environmental and public concerns over cyanidation, there has been a large amount of research into viable alternative lixiviants. Despite these studies, there is little published data directly comparing the kinetics of gold leaching for each of these alternatives: most of the literature is concerned with gold extraction from ores. This paper presents a detailed kinetic study of gold leaching in cyanide, armmonia/thiosulfate and chloride/hypochlorite solutions. The gold leach rates were measured using a rotating electrochemical quartz crystal microbalance (REQCM). This instrument allows the mass of a gold sample to measured in?situ, with a sensitivity of less than 10 ng. From the results of these studies, it is possible to select experimental conditions where the leach rates of the alternative lixiviants are similar to that for the traditional cyanide system.

Jan 1, 1998

By Ray Y. Lin

This study explores the formation of sodium pyrosulfate in molten sodium sulfate resulting from dissolution of SO3 at temperatures between 1160 and 1250 K. Solubility of SO3 in Na2SO4 melts at temperatures between 1160 and 1250 K under gas mixtures of SO2, O2 and argon was investigated applying a thermogravemetric analysis (TGA) technique. The activity of Na2O in the melt was determined with a high temperature electrochemical cell (ECC). Results showed that the SO3 solubility in molten Na2SO4 increases with decreasing temperatures and increasing SO3 partial pressures. Enthalpy of SO3 dissolution in molten Na2SO4 was calculated to be -119 kJ/mol for infinite dilute solutions. Thermochemistry of Na2SO4-Na2S2O7 melts was analyzed based on information obtained from both TGA and ECC techniques. Detailed examinations of the earlier low temperature measurements in the Na2SO4-Na2S2O7 system along with data from this study reveal that the solution behavior between Na2SO4 and Na2S2O7 can be satisfactorily treated as regular with the interaction parameter, , being 2.7 kJ/mol. The phase diagram and the field of SO3 partial pressure has been generated with the thermodynamic calculation using a regular solution approach.

Jan 1, 2006

By Mikiya Tanaka, Mikio Kobayashi, Mansour A. S. A1Ghamdi, Kenji Tatsumi, Yukinori Saiki, Hirotaka Senba

"In order to recover nickel ion in a spent electroless nickel - phosphorus alloy plating bath and, at the same time, to remove impurities such as iron and zinc, the applicability of solvent extraction with LlX84I as the extractant has been investigated using actual spent solution. Although the extraction efficiency of nickel from the spent solution is considerably lower than that from the nickel sulfate-nitrate solution, nickel in the spent solution is selectively extracted with high efficiency at the pH of 6 - 7. The extracted nickel is effectively stripped by sulfuric acid at a pH of less .than· 3. On the basis of these results, a· flowsheet for recovering nickel from the spent solution is proposed Chemical equilibrium calculations of the spent solution has shown that the complex formations of nickel with anions such as lactate and phosphonate ions become predominant in the pH range between 2 and 6. This results in the depression of nickel extraction efficiency from the spent solution as compared with that from the .nickel sulfate-nitrate solution. By combining these aqueous equilibrium calculations with the· extraction model considering the extraction stoichiometry and the aggregation of the extractant in the organic phase, the extraction behavior of nickel is quantitatively predicted.IntroductionElectroless plating is indispensable for the recent advanced industries such as the electronic and mechanical industries. Electroless plating baths are repeatedly used by supplying the metal salts; however, the accumulation of the counter anions of the metal ions, the components formed by the oxidation of the reducing reagents in the plating baths, and the metal ions as impurities dissolved from the surface of the objective materials degrades the· quality of the plating. Thus, the baths are finally treated by a precipitation method to form a large amount of metal sludge, which is disposed in dumping sites. Therefore, from the standpoints of environmental protection and resource preservation, it is highly desired to establish a recycling process of the plating baths with minimum emission. Solvent extraction seems to be one of the 'suitable methods to recover metals from the spent electroless plating baths, because the concentration of the metal ion in the baths is relatively high, which is advantageous to solvent extraction as compared with the ion-exchange and adsorption methods. Some studies about the application of solvent extraction have already been carried out using simulated spe11t electroless plating baths [1-3]."

Jan 1, 2000

By Daniel A. Norrgran

Grinding ball fragments discharging from SAG mills and ball mills causes extreme wear to downstream processing equipment. These ball fragments, recirculating in a milling circuit, will cause excessive wear to sumps, pumps, hydrocyclones, and interconnecting piping. A magnetic separation system to remove grinding ball fragments from the mill discharge has been developed and successfully applied in the milling circuit. This magnetic separation system - termed Trammel Magnet - was first applied at the Escondida copper concentrator in Chile. The Trommel Magnet consists of an arc of permanent magnets mounted at the discharge end' of the tommel screen. The magnetic arc attracts the ball fragments and removes them from the process stream. This retrofitted magnetic separation system removed 126 metric tons of ball fragments from the circulating load of a. single ball mill in the initial 24 hour period. The mill has since stabilized and the magnetic separator is currently removing 7 metric tons per day of ball fragments. The retrofit of the Trommel Magnet has: 1. Extended the pumpp life and the hydrocyclone life approximately 300 percent. 2. Provided a 5 percent increase in the throughput of the mills by removing grinding ball fragments that contribute very little to the grinding process. Variations of the Trommel Magnet have also been developed for removing grinding ball fragments directly from the mill discharge without the use of a trommel screen. In each case, permanent magnets are used to collect the ball fragments from the mill discharge stream prior to reporting to the sump. These other systems have been designed and fabricated for in-plant test work.

Jan 1, 1999

By Luciano B. Oliveira, Luis G. C. Marques, Sergio N. Monteiro, Marcos V. M. Fagundes

"Biodiesel production is normally associated with large plantations of oily vegetables such as soybean and colza, in large rural areas. However, in the municipal limits of the city of Rio de Janeiro, southeast of Brazil, biodiesel is being produced from wastes commonly generated by typical urban activities such as sewage sludge, discarded fat from meat markets and post-used cooking oils. In the present work, the experience of producing biodiesel from urban wastes in Rio de Janeiro is assessed. The type of precursor materials, equipments and logistics are presented. The environmental and economical advantages as well as the drawbacks are discussed.IntroductionThe interest for a liquid fuel that could substitute those obtained from petroleum started more than one hundred years ago when Rudolph Diesel tested his no-spark internal combustion engine, impelled by compression, with peanut oil. By that time, petroleum was beginning to be extracted in large scale and no one was concerned with the future environmental problems and its eventual depletion. In the last century, the successful association of petroleum based fuels with the automotive industry was an almost insurmountable obstacle to any attempt to use nonmineral oils [1]. In addition to the greater efficiency and, by then, lower price of the diesel from petroleum, the use of plain vegetable oils introduced undesirable carbon deposits and reduced the engine lifetime. Today, the situation is reverse. The continuous increase in the price of petroleum and, above all, its contribution to climate changes are strongly motivating the use of biofuels to replace those obtained from fossil fuels such as petroleum, natural gas and coal [2].In the case of the common petroleum derived diesel, many countries are now engaged in large scale substitution programs. The USA should produce more than 700 million litters of biodiesel, while the European Community is expected too produce around 6.5 billion litters in 2008. In Brazil, the federal biodiesel program imposed a minimum of 2% addition to the common diesel. This would demand a production of 800 million litters in 2008 [3]. The Brazilian biodiesel is made from a diversified source of vegetables mainly castor bean, African palm and soybean. The main producers are agrobusiness firms located in large rural areas of the Brazilian hinterland [4]."

Jan 1, 2008

By Ann M. Hagni

Flash reduction of zinc oxides is an alternative, environmentally safe method to leaching and electrowinning for zinc recovery. Zinc and lead are volatilized in a flash reactor, a non-hazardous residue is generated, and the fuel source is inexpensive coal in the flash reduction process. Results from experimental laboratory tests yielded low zinc recovery for this process. Mineralogical and textural characterization of the residues from the flash reduction tests for different feed materials and temperatures were conducted to determine the cause for the low zinc recovery. Reflected light microscopy, cathodoluminescence microscopy, scanning electron microscopy-energy dispersive spectroscopy, and X-ray diffraction were utilized in this applied mineralogical research. The original zinc calcine is composed primarily of fine-grained, iron-bearing zincite particles, 25-40 um in diameter, in a porous texture. Pellets processed at 1150°C were found to produce reaction rims of franklinite-magnetite-jacobsite solid solution that are 125-200 um thick and surround cores of unreacted iron-bearing zincite in a Zn-Fe-Si-Ca glass matrix. The reaction rims have subsequently oxidized to form an outer 10 ~m thick rim of hematite. Slags from calcines processed at 1275°C are primarily triangular particles with porous centers, cenospheres, and spheres of iron-bearing zincite, in addition to rectangular particles composed of non-porous franklinite-magnetite solid solution cores with iron-bearing zincite rims. Slag particles from calcine processed at 1200°C are predominantly 100-250 ~m triangular-shaped, spheres, and cenospheres containing fine-grained franklinite and franklinite-magnetite solid solution in an iron-bearing zincite matrix. Slag from calcine processed at 1300°C are also predominantly 1 00-250 um triangular-shaped, spheres, and cenospheres but contain coarser-grained iron-bearing zincite. The zincite in the penets and the slags typically contain 10-20% iron. Based upon these mineralogical observations, it is concluded that the significant amounts of iron in the zincite prevent volatilization of the zinc in the flash reduction process.

Jan 1, 1995

By Michael J. Nicol

Growing environmental and occupational safety concerns about the use of cyanide in gold processing has increased the interest in more acceptable alternatives. The most likely of these is thiosulfate. However, the thiosulfate process lacks a proven in-pulp method of recovering the dissolved gold, because activated carbon is not effective for the absorption of the gold thiosulfate complex .. Anion exchange resins do offer a possible route for in-pulp recovery. This paper describes work aimed at the evaluation of the effectiveness of commercially available anion exchange resins for the recovery of gold from thiosulfate leach liquors? and pulps. It has been found that strong-base resins are superior to weak-base resins in that they have a larger capacity, which assists in reducing the competition from other anions within a leach solution. Further studies with a selected commercial strong-base resin have shown that competing polythionateanions (particularly tri-and tetrathionate). Lower the maximum possible gold loading but that gold is selectively recovered over other base metal anions in solution. Kinetic experiments found that while? competilig anibns did not affect the initial rate? of gold loading it was important to minimise the contact time of the resin in solution so to prevent displacement of loaded gold by competing anions over longer times. A small-scale resin-in-pulp plant investigation showed gold can be recovered from a leach pulp by a strong-base resin to yield gold loadings of 3000 mg/L, barren pulp containing less than 0.05 mg/L of dissolved gold and. copper loadings of 500 mg/L. Loaded copper was displaced gold and at a loading of 2000 mg/L gold the copper loading was minimal «500 mg/L). The resin was found to recover gold adsorbed on the solids that would, otherwise have. reported to tails if a solid/liquid separation method were used. A patented two-step elution process in which copper and then gold are separately eluted from the resin is also discussed.

Jan 1, 1998

By J. M. Demarthe

The recovery of minor metals from zinc concentrates is dependent on the process used for their treatment. The behaviour of gennanium and indium in pyrometallurgical processes such as the Imperial Smelting furnace or the cupola furnace is of practical importance. The .Anaconda process for the treatment of zinc leach residues is not well suited to the recovery of valuable minor metals, and new technologies must be studied. In this regard, a solvent extraction process, using Kelex 100, developed by Minenet Recherche for the recovery of gennanium from dilute sulphate leach solutions is described. Also, new hydranetallurgical techniques in chloride media can be applied to the purification and concentration of minor metals depending on the stability of their chloro-complexes and the valency of associated inpurities. A synthesis of methods is proposed to address the problems related to the recovery of valuable minor metals in the zinc industry.

Jan 1, 1990

By Robert Vidal

The performance of a laboratory-scale cell for the electrolysis of an aqueous chrome alum solution was studied. Electrode potentials, pH, and Eh were recorded. An optimum catholyte pH of about 2.5, consistent with information from the literature was observed. Values exceeding this range resulted in a precipitate formation and are detected by wavering cathode potentials. The role of anodically produced dichromate ions was investigated by chemical analysis. It was found that the steady state concentration of dichromate ions varies inversely with fluid flow from catholyte to anolyte. This concentration was also reduced with the use of precious metal coated titanium anodes.

Jan 1, 1994

By Majid Sarkari, Hossein Atashi, Farhad Fazlollahi

"The aim of this research work was to prepare the efficient catalyst to purify pollutant output gases such as SO2 , NO2 and CO. This catalyst, lanthanum cobaltat (LaCo03) was prepared by the proper method in the analysis laboratory of Tabriz Oil .The first materials were chosen through calcination operation and temperatures of operation related to the Tamman temperature, therefore the basis for the first material of catalyst was nitrate and aqueous and since we had no availability to lanthanum nitrate, lanthanum oxide was used to prepare the nitrate one. Before all else, the first materials of catalyst were mixed together with the equal mole proportions and then, at the lower and upper temperatures of Tanunan temperature, calcination operation was carried out. To determine the molecular structure, the XRD analysis was utilized and specified that prepared lanthanum cobaltat was sixth aqueous and had the crystal structure type Triclinic.IntroductionLaCo03 has presented a vast interest because of its special electrical, magnetic and catalytic properties [1-4]. The catalyst LaCo03 can be prepared by means of several methods such as spray drying, freeze drying and also co-precipitation [5-12]. Some methods including hydrothermal, sol gel and citrate [13] This material usually has been synthesized by ceramic method and certainly the high temperature for the calcination operation. [14]. Lanthanum catalysts have been researched because of having such an active state [15]. One of the unique properties of this catalyst is the simultaneous conversion of pollutant elements. Nowadays CO oxidation has important applications in environment protection, such as indoor air cleaning and automotive exhaust treatment. LaCoO3 is one of the most important catalysts for CO oxidation."

Jan 1, 2013

By Viviane Tavares de Moraes, Denise Crocce Romano Espinosa, Jorge Alberto Soares Tenorio, Adriana Johanny Murcia Santanilla

"Increasing volumes of solid waste are generated worldwide, due to the continuous technological advances, the electronic scrap is part of these waste, requiring the study of recycling processes to stimulate this activity or the reuse of its components. The separation of nickel from sulphate leach solution, which also containing iron, zinc and aluminium was carried out using bis-(2,4,4-trimethylpentyl) phosphinic acid (Cyanex 272) as extractant, in order to determinate the effects of pH and temperature. The number of stages required for extraction was also assessed. The results showed that the metal extraction increased with increasing pH. On the other hand, increasing temperature was not favorable for all metals. However, under conditions used in this paper the purification of solution containing nickel was possible.IntroductionIncrease in the demand of metals in the world for use in industry causes a great exploration of natural resources. One outcome of this is increased investigations for the recovery of metals from industrial wastes. Nickel is found in wastes, such as batteries and electric and electronic devices, this kind of waste becomes a significant source for metals recovery. Since nickel is also present in printed circuit boards, which are associated with electric and electronic equipment, it can be recovered from this kind of waste through different techniques. It is important to highlight that iron is generally associated with this scrap [1] and for its removal chemical precipitation is often used. On the other hand, the solvent extraction process is widely used for treatment of leach liquors, because it can be produce high purity solutions [2, 3]. This technique is based on the purification of solution using contact between a liquor leaching and the immiscible organic solution, which contains an extractant that promotes the desired metal transfer [4]."

Jan 1, 2012

By Guozhu Ye

Hydrometallurgical zinc recovery from EAF dust has several advantages compared to pyrometallurgical alternatives in terms of low temperature operation, lower energy consumption and higher flexibility. Many hydrometallurgical processes have been suggested and tested over the years without success. The main reasons are: -Low leaching yield of zinc due to the fact that a high fraction of ZnO in the EAF dust exists in the zinc ferrite structure which makes selective leaching of ZnO not possible -Many of the proposals could not handle the halide in the EAF dust To eliminate these two disadvantages, two zinc ferrite elimination concepts have been tested and developed in the REZIN project of the EU 5th Framework Programme. The two concepts for zinc ferrite elimination could be shortly described by the following chemical reactions: A. ZnOFe2O3 + 2CaO = Ca2Fe2O5 + ZnOfree B. ZnOFe2O3 + C = Femet + CO/CO2 + ZnOfree These two concepts were investigated in details in combination with a subsequent leaching step using the novel EZINC process for recovery of zinc from EAF dust. Leaching of pretreated samples has shown great increases of a zinc recovery yield. A zinc recovery of over 90 % could be reached, as compared to about 50 % for no-pretreated samples. This paper will describe the two concepts in details.

Jan 1, 2006

By Bernd Kos

The management of waste materials in the aluminum industry is as important as in other basic industries. Due to the high value of the-by products of the melting process and their toxic properties we took the challenge to develop a process technology to reduce the environmental impact and to help industry to get a better yield of their by products/raw materials. In melting operations metal losses due to oxidation are nearly unavoidable, the amount of such losses, however, can be controlled. Aluminum dross actually is a by product and any shop would like to get rid of it in the most economic way. This by product still contains up to 70% valuable metal! In the present work we describe possibilities to separate metal and residues for further processing. Recycling of metal concentrates, selling of dross and dumping of the residues have been the typical solutions up to now. But there are technologies available which are designed to reduce the waste to a minimum or even avoid it altogether. Such alternatives are processing of the dross into materials which can be reused in other industrial processes in order to avoid any dumping. This can be done by separating the metal and the residues by centrifuging and further use of the residues in the chemical or refractory industry. ECOCENT means economical and ecological recovery of aluminum by centrifuging of hot dross. This process, developed by FOCON Austria, is based on the idea of treating the hot dross as quick as possible in a single operation to avoid exothermic losses, intermediate storage and unnecessary handling as well as to save energy. In the ECOCENT process the hot dross is fed without any fluxing salt additions into a converter where the relevant parameters for separation, like temperature and viscosity, will be adjusted. Further big lumps of dross are ground into smaller pieces in order to improve the later separation of the metal. After homogenizing and adjusting the temperature, the hot dross is poured as quickly as possible into a centrifuge. In the ladle or alternatively the mould of the centrifuge the centrifugal forces are used for the separation of aluminum from aluminum oxide, the major constituents of dross. The separated pure metal can either be discharged liquid or as solidified aluminum ring. The design of the device for the production of liquid or solid metal is almost identical. As soon as the centrifuging is finished the liquid aluminum can be poured back into the furnace or can be used for ingot pouring. After the pouring of the metal the "dry" residues are removed just by turning the ladle. Alternatively the aluminum solidifies in the mould and is discharged as a compact ring. The separation of the residues from the aluminum ring is automatic. Due to the batchwise operation the composition of the metal is the same as in the skimmed furnace of origin. The complete treatment cycle needs about 40 minutes. The recovery rate of aluminum is better than 90% of pure metal. This technology is highly flexible by its nature and can easily accomodate various operational requirements. The consumption of energy is more than 50% lower compared to conventional dross processing as the ECOCENT process is using the inherent energy of the hot dross. These extremely good results are not dependent on the aluminum content of the dross even from very dry dross most of the metal can be recovered. The main advantages compared to conventional dross processing are the high recovery rate, the known analysis of the metal and the immediate reuse of the recovered aluminum. The high recovery rate and the pure metal result in a short amortization period. The compact ECOCENT unit needs a minimum of space since extensive handling can be avoided. The electronically controlled process needs no cooling water and is simple, safe and environmentally sound. The residues are free of fluxing salts, their content of metallic aluminum is low and the environmental problems are thus greatly reduced.

Jan 1, 1995

By Felipe Daroch, Maria C. Ruiz, Rafael Padilla

Copper concentrates with high arsenic contents must be pretreated before conventional smelting to prevent environmental pollution with arsenic compounds. In this work, experimental results concerning the selective removal of arsenic and antimony from copper concentrates are presented. The process consists of an alkaline digestion using concentrated NaHS-NaOH solutions to transform the arsenic and antimony sulfides into soluble compounds. A water leaching follows the digestion to dissolve the arsenic and antimony, leaving clean copper sulfide solid residues. The laboratory scale tests were carried out using a copper–arsenic concentrate with 15.05% As and 1.42% Sb. The results showed that the most important digestion variables were temperature and concentrations of NaHS and NaOH. Over 97% of arsenic and 92% of antimony could be removed in 10 min of digestion using 8.9 M NaOH and 100% excess of NaHS at 80 °C. The subsequent water leaching was performed at 80°C for 20 min.

Jan 1, 2015