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By H. Aminian

Copper electrowinning (EW) is an important process in connection with the solvent extraction to produce pure and marketable copper cathodes. A phenomenological model was developed to simulate the copper electrowinning process. The simulator is used to predict the operation of the Mines Gaspe pilot plant electrowinning cells put in operation in 1996. Results confirm the potential of the simulator that would subsequently be used for student training, process optimization and assessing the performances of control strategies.

Jan 1, 1999

By I. Sofia Fernandez del Rio

This paper describes a process for the treatment of the dusts generated during the operation of blast and reverberatory furnaces in the lead smelter, to remove zinc, cadmium, arsenic and halides from the circuit. The process consists of a Pefloles' developed leaching/purification stage and a solvent extraction process developed by Lurgi. The plant capacity is 5,000 tonnes Zn/year. The feed to solvent extraction contains 8 g/1 Zn. Impurities such as copper, iron, arsenic and cadmium are removed by conventional cementation processes. The cadmium product is 99.99 % pure. The solvent extraction process consists of two extraction stages, one washing stage and two stripping stages. D2EHPA is used as the extraction agent and 25% ammonia as the neutralizer. The rich-zinc solution is sent to the electrolytic zinc plant for zinc recovery. The raffinate produced, which is a mixture of ammonium sulfate and chloride, is used for agricultural applications.

Jan 1, 2000

By D. Quattrini

The aim of the present work is to present the gas chromatography (GC) as an alternative method of analysis in the thermal decomposition of calcium carbonate. Therefore, a furnace/GC on-line system was employed to study the kinetics of the reaction, measuring the CO2 produced in the decomposition. One of the advantages of the GC method is the possibility to perform an in-situ characterization and quantification of the gaseous products to obtain kinetic parameters, besides the method is simple and shows a good reproducibility. The decomposition of calcium carbonate was carried out in isothermal conditions at temperatures from 655 to 715°C with nitrogen as purge gas. Several gas velocities were used to determine the adequate flow that minimizes the effect of external mass diffusion as rate controlling step. It was made a preliminary analysis of the sample size influence on the reaction rate. The activation energy of the reaction was determined by Flynn method. The value obtained was in a good agreement with other authors. On the other hand, gravimetric measurements were employed for compare GC results.

Jan 1, 2006

By Carlos Eduardo Gomes de Souza, Luis G. S. Sobral, Paulo A. Medeiros da Silva, Selma G. F. Leite, Renata de B. Lima

"The use of mixed cultures of acidophilus microorganisms that act in different temperature ranges, aims at speeding up the digestion of chalcopyrite, highly refractory sulphide mineral, the major mineral in the flotation concentrate of Caraíba Mining Co., with an attractive processing cost. The concentrate under consideration contains mainly chalcopyrite (CuFeS2) and bornite (Cu5FeS4) with contents of, approximately, 70 and 30%, respectively. It was observed in this study, the performance of consortium of mesophiles, moderate and extreme thermophile microorganisms, in the oxidation of the aforementioned sulphides minerals, evaluating operational parameters such as pH of the leaching solution, the reaction temperature and redox potential, with consequent extraction of 80% of the concentrate copper content within 60 days of bioleaching. Such high copper extraction was achieved in column bioleaching tests.INTRODUCTIONThe solubilization of metals by the application of microorganisms from the mineral ores and the subsequent recovery of metals from solution are referred to as bioleaching (Rohwerder, T et al, 2003). This is an economical method for the recovery of metals from minerals; especially lowgrade ores, overburden, and waste from current mining operations which requires moderate capital investment with operating cost (Watling, 2006).Furthermore, bioleaching is generally more environmentally friendly than conventional metal recovery processes such as concentration and smelting. Those physicochemical metal extraction processes generate sulphur dioxide, a toxic emission that is increasingly the target of regulatory legislation (Stott et al., 2000; Olson et al., 2003). Bioleaching of chalcopyrite is the key industry target. The main problem hindering commercial application of chalcopyrite bioleaching is the slow dissolution rate (Fu et al, 2008).Dissolution of acid-soluble sulphide minerals such as sphalerite, and to a lesser extent chalcopyrite, occurs by a combination of ferric iron and proton attack via the polysulphide pathway (Rohwerder et al., 2003)."

Jan 1, 2008

By Jack S. McPartland

Historically, research on thiosulfate leaching of precious metals ores has been focused on processing of difficult to treat ores. Thiosulfate leaching of ores and concentrates containing sulfide minerals, copper, manganese and preg-robbing carbon constituents has been evaluated. Cyanide leaching is generally considered an efficient, environmentally acceptable means for processing of non-refractory precious metal ores, Consequently, commercial processing of finely disseminated, oxidized precious metal ores is normally accomplished using alkaline cyanide leaching. Recent changes in regulatory climate have, however, called into question the acceptability of cyanide leaching in a number of locations worldwide. In some cases where the use of cyanide is being questioned, thiosulfate leaching may provide an acceptable alternative. Developments in thiosulfate leaching of precious metal ores are reviewed in this paper.

Jan 1, 1999

By Zenon R. Llanos

"The disposal of spent hydroprocessing (HDP) catalysts in the petroleum refining industry has been a concern in the past due to their classification as listed hazardous wastes. However, because these catalysts have higher metal concentrations than regular ores, and the recent surge in prices for molybdenum, vanadium, nickel and cobalt what used to be considered as a liability for generators is now viewed as a valuable renewable source of strategic metals. At the same time the generation of spent catalysts has steadily risen due to new environmental regulations for low sulfur fuels and an increased appetite of gasoline consumers. This paper will examine spent catalyst market and the role played by Gulf Chemical & Metallurgical Corporation in the reclamation of metals over the last sixty years. Introduction Hydroprocessing (HDP) catalysts are used in petroleum refineries for two main applications: desulfurization and cracking. The catalyst support is alumina or mixtures of alumina and silica. Active metals include molybdenum, nickel, cobalt and tungsten. The selection of catalysts depends on the application and sometimes the cost. The life cycle of HDP catalysts is represented in Figure 1. The catalyst cycle in a reactor varies from continuous to one-two years. Catalysts used in various refining processes are deactivated by coke, sulfur, vanadium and other impurities in the refinery feedstocks and become spent. Refineries can optionally send the spent catalysts for regeneration, metals reclamation or landfilling. Catalysts used for refining heavy crudes often can not be regenerated. Catalysts used with light oils can be reused twice or three times after regeneration. When the option for regeneration is not viable, spent catalysts are send metal reclamation facilities or landfills."

Jan 1, 2008

By Igor Zh. Bunim, Valentine A. Chanturiya, Alexey T. Kovalev, Irina A. Khabarova, Elizaveta V. Koporulina

This paper presents new theoretical and experimental data on possible mechanisms for the formation of micro- and nanophases on the surface of sulfide minerals un der the effect of high-power nanosecond electromagnetic pulses (HPEMP). The gas outflow from nanosecond breakdown channels of sulfide minerals under the effect of HPEMP is considered, with allowance for the condensation of iron vapors. The condensation of matter in an outflowing jet is shown to be an effective mechanism for structureal and chemical transformations of sulfide surfaces. It is established that electrode potential of pyrrhotite is moved together in the negative party owing to formation of iron oxides (hydroxides) and iron sulfates by HPEMP, that provides decrease of xanthate sorption and reduction flotation extraction of this sulfide, whereas electrode potential of pentlandite gets more positive values at the expense of additional formation of element sulfur, that causes increase of xanthate sorption and, as a consequence, increase of nickel sulfide extraction.

Jan 1, 2012

By David Langberg

Recovery of dissolved copper from discard slags is a critical consideration affecting the economics of copper smelting. Slag cleaning is frequently carried out in electric furnaces, however reduction by injection of natural gas in a holding furnace may offer a lower cost alternative in some circumstances. As the residence time of the injected gas is short, the factors controlling the rate of reduction need to be clarified in order to optimise the design of the slag cleaning furnace. A series of medium scale (200 kg) reduction tests to investigate the rate of reduction of copper-containing slags by injection of natural gas-nitrogen mixtures between 1150-1250C was carried out by CSIRO Minerals. The composition of the gas in the top-space of the reactor was found to be significantly more reducing than the slag, indicating that thermodynamic equilibrium was not established between the slag and the gas in the bubble plume. An apparent first order rate law was observed between the rate of oxygen elimination from the bath and the magnetite concentration of the bath. The dissolved copper concentration was closely correlated with the oxygen potential of the slag, suggesting a partial equilibrium between the dissolved components of the slag. The utilisation efficiency of the natural gas decreased as the natural gas flow rate was increased. The results of the tests tend to indicate that the rate is controlled by a mixed reaction kinetics/ mass transport mechanism. The work was supported by Xstrata Copper ? Mt Isa Mines.

Jan 1, 2006

By M. Olper

Today, copper production from direct leaching of oxidized copper ores followed by solvent extraction-electrowinning (SX-EW) accounts for about 15% of the total primary world output. SX-EW is a well-accepted process with an operating cost in the range 16-20 cents/lb. copper for small and medium size plants, depending on the plant size and local conditions. However, this technology presents some drawbacks that affect the operating cost and cause environmental concerns. ENGITEC and Paques Bio Systems have developed a new process that avoids the solvent extraction step and operates the copper electrowinning step at a lower cell voltage because of the depassivation of the anodic reaction. The consequence of this new concept is that the direct operating cost is in the range 10-12 cents/lb. copper. This new process is composed of the following steps: ? Selective precipitation of copper from leach solutions by biogenic H2S, yielding CuS and regenerating acid ? Leaching of the CuS with a ferric fluoborate solution to dissolve copper and produce elemental sulphur that is recycled back to the H2S biogeneration step ? Electrowinning of copper fluoborate solution in a diaphragm cell with the ECUPREX® Process, producing copper cathodes and regenerating the ferric fluoborate solution to be recycled back to the leaching step ? Biogeneration of H2S from the elemental: sulphur generated during the leaching step, with the nutrient source for the anaerobic bacteria selected form a wide range of organic substances and/or some industrial by-products containing carbon and hydrogen This paper describes all process steps with particular reference to the biological H2S generation technology. Also discussed' is the capability of the ECUPREX® Process to treat copper sulphide concentrates and copper matte.

Jan 1, 1999

By Wang Haibei

China is the important country in terms of Ga, Ge reserves and products. These elements usually associate with lead and zinc ores such as in Fankou, Dachang and Lanping mines. Until now these metals could not be extracted from zinc residues effectively. The main reason is that it is difficult to separate zinc and iron. BGRIMM has carried out considerable research on this subject and some hydrometallurgical processes were developed. Zinc residues were pressure leached with a reducing agent such as zinc concentrates or SO2 at 110~130C. The final concentrate of H2SO4 was 30~50g/L. The metals such as Zn, Fe, Ga and Ge were dissolved into solution. In the leaching residue Pb and Ag could reach 20% and 2000g/t. The feed of solvent extraction was prepared from the leaching solution by pre-neutralization ? precipitation of Ga, Ge and acid dissolving. Then Ga and Ge were extracted by solvent extraction through P204 and G315 produced by BGRIMM. After stripping, metallic Ga was produced by electrowinning. GeO2 was produced by precipitation. The iron in raffinate was removed by the hematite process. The solution after removal of iron came back at the zinc neutral leaching stage. In 2003-2004, pilot tests were finished in BGRIMM in cooperation with Fankou Lead and Zinc Mine Ltd. And the extraction rate of Ga and Ge in the leaching stage was 94% and 83% respectively. The total recovery rate was 90% and 80%. It is estimated that the technology has a wide commercial use in the coming five years.

Jan 1, 2006

By Paykan Safe

The primary source of fugitive gas emissions in most copper smelters are the Peirce Smith converter operations. The modem trend is towards installation of secondary gas collection systems which are intended to collect fugitive gases from charging, standby, and skimming operations. These have been installed with varying degrees of success. Often, the major source of emissions from the converter area is leakage of process gas from the primary hoods when the converter is blowing. This gas is typically collected by the secondary system and discharged to atmosphere or scrubbed with an alkaline agent. Those smelters considering installation of secondary hoods or scrubbing of gases from secondary systems should first address the issue of gas leakage from the primary hoods. Improving the primary hood gas collection efficiency will often be more cost effective than installing secondary hooding. In the case of secondary gas scrubbing, it will significantly reduce the reagent consumption and operating cost of the scrubbing system. This paper examines the parameters that determine whether or not a primary hood will effectively collect process gases without leakage and demonstrates, using Computational Fluid Dynamics (CFD), the effects of variations in these parameters on the overall performance of the hood. It also looks at the application of CFD techniques in the design of secondary hoods and presents a summary of measured emissions from converter buildings.

Jan 1, 2002

By Jan Steinhoff

The design options of a gravity separator are still limited and rely on the study of settling behavior. A methodology will be presented where an experimentally given inlet droplet size distribution (DSD) is the basis for the calculation of the dispersion layer in a gravity separator. A pilot-scale continuous gravity separator is presented and CFD (computational fluid dynamic) results are validated. A transmitted light measurement technique for the determination of the DSD is presented up to a holdup of 15% dispersed phase. The resulting DSD was in the range of 20–2000 μm depending on flow rate and phase ratio. Furthermore, correlations of the real DSD with the settling behavior of the dispersion in a settling cell are discussed. The new approach to the description of gravity separators will be presented and the applied CFD methods showed good results with the system water/paraffin.

By Junhong Noh, Kug Sun Hong, Jung-Kun Lee, Bo Ding

"The photocatalytic splitting of water into H2 and O2 by oxide nanoparticles has received much attention. However, the full potential of photo-catalysts for efficient hydrogen generation out of water has not been fully realized yet due to unresolved limitations including the low electrical conductivity and ineffective carrier extraction. Here, we report composite oxide materials consisting of 1-dimensional (1-D) transparent conducting oxide (TCO) core and TiO2 shell. Highly conductive ITO nanowires were grown on a flexible SUS mesh as a core component. The photoelectrodes consisting of these 1-D nanocomposites have increased carrier mobility due to the TCO core, while the TiO2 shell provides the photocatalytic functionalities. In addition, the built-in-potential at the interface between TCO core and the TiO2 shell improves the collection of charge carriers from TiO2 to TCO. These factors altogether contribute to increasing the photocurrent of the device under light.I. IntroductionPhotocatalytic behavior of semicondcutors has been extensively explored since it was discovered in TiO2 in 197Os. When TiO2 is exposed to UV light, the light is absorbed and electron/hole pairs are generated in the conduction and valeence bands. Holes in valence band will oxide/mineralize pollutant target directly or indirectly (via mediator hydroxyl radical). If the adsorbed A is O 2, O 2 will react with electron from conduction band to generate hydroxyl radical as described in the second set ofreactions. The photocatalytic reaction is schematically explained in Figure 1.Photoelectrochemical (PEC) cells using the photocatalytic reaction have attracted emerging interest as a potential route to convert solar radiation into useful forms of energy by reaction such as water splitting to generate hydrogen1 or the reduction of carbon dioxide.2 Another application ofphotocatalysis is water splitting and CO2 reduction, both of which utilize the electrons that are optically excited to the conduction band. 3•4 For this purpose, the conduction level of the semiconductor should be higher than hydrogen production level (EHZ1HZO) while the valence band should be lower than water oxidation level (Eo21112O). Electrons and holes will be generated on the semiconductor site, and holes generate O 2 at semiconductor site, while electrons will migrate to counter electrode to execute reduction forming H2. In addition to that, materials should be chemically stable to resist photocorrosion and have long lifetime of electron/hole pairs. TiO2 is a suitable material from the viewpoint of band arrangement and chemical stability requirement"

Jan 1, 2012

By A. Robles

The main goal of the present work is to propose a viable alternative for selective arsenic elimination from copper smelter flue dust without the need of a global leaching scheme for all the individual components of the flue dust. Using this alternative, the inherent copper recovery problems are avoided. Arsenic precipitation is also considered for regenerating the solution and completing the process cycle. The experimental results for arsenic extraction and precipitation are satisfactory. Concentration of NaOH used was relatively low. The main reason for succeeding in high arsenic extraction and low NaOH consumption is due to the previous water washing of the flue dust. Water washing dissolves much of the iron and copper that are present in certain percentage as sulphate.

Jan 1, 1999

By Ronald C. Askin

Dredging is a common method of remediating ponds containing contaminated wastes. However, dewatering of the dredged solids is usually not well integrated with the dredging phase. As a result, overall project efficiency can be poor. Specifically, since dredges deliver material in a widely varying slurry form and since dewatering presses require the delivered material to be uniform, union of the two systems often results in inconsistent operation of the overall process. In an effort to enhance overall dredging and dewatering process production rates as well as minimize the return of suspended solids in the decant water, a new process was developed to provide a consistent dredged sludge for delivery to the press. This paper discusses modifications made to a conventional dredging and dewatering process to improve production rates and dewatering capabilities. These modifications are applicable to any project where efficient solids dewatering is required and where returning decant water must be visually free of suspended solids.

Jan 1, 1996

By Andrew Shabalin, Vladimir Skorohodov, Svetlana Babaeva, ?lga Makovskaya

"At processing of some kinds of wastes (electronic scrap, secondary materials, spent nuclear fuel) in nitric acid solutions, and also in technology of silver refining, the significant amounts of palladium and platinum passes into a solution. The ion-exchange concentration of palladium and platinum in nitric acid solutions (5-500/dm3) are investigated. More than 30 various classes of ionites are tested. The most chemically resistance resins at the given conditions are identified. It is shown, that the maximum sorptive capacity to studied metals at high acidity the complexing, synthetic and inorganic sorbents possess. To definition of platinum metals sorption optimum conditions the kinetics is studied, isotherms of a sorption at various parameters from nitrate solutions are obtained. The conditions of the platinum and a palladium desorption from the pregnant sorbents and its regeneration with the subsequent reuse of materials were defined. The raw materials containing precious metals have very diverse composition and physical properties. Commonly the materials are processed by hydrometallurgical way. If gold or PGMs there are in raw materials to its opening hydrochloric acid solutions are applied. As an oxidizer nitric acid, hydrogen peroxide, gaseous chlorine, etc are used. Nevertheless, at processing of argentiferous materials and preliminary treatment of a waste including the spent nuclear fuel, nitric acid solutions are often used and the specified metals in some extent pass into solution [1]. Therefore selective extraction of PGMs from nitrate solutions is an actual problem. In the present work the ion-exchange concentrations of palladium and platinum in nitric acid solutions (5-500 g/dm3) are investigated. At the testing more than 30 various classes of ionites the most chemically resistance resins at the given conditions are identified. These resins are synthesized on the base of polyacrylate, styrene-divinylbenzene and vinylpyridine. For a selection of the most effective resin among what are made in Russia and overseas, a number of ionites with various functional groups were studied. Influence of functional groups type on a PGM sorption is shown for extraction of a palladium as an example (table 1). The presented data shows, that palladium concentration in a phase of ionites depends on sorbent type. If the increasing of solution acidity essentially reduces palladium sorption by sulfonic cation-exchange resins (KU-2×8) than its sorption by strongly basic anionites is approximately equal. Intermediate position is occupied by complexing sorbents. The latter (AN-31, SN-3, ANKB-35, Lewatit TP 207, Purolite S 930) are the most effective for extraction of PGMs from nitrate solutions from the point of view of capacity value. According to [2], solution behavior of Pt (II) and Pd (II) are similar. As is known from coordination chemistry, ligand environment of the metal ions substantially impacts to character of electronic spectra. The figure 1 shows the results of measurements of optical density of platinum bearing solutions with various concentration of nitric acid at ?=400 nanometers"

Jan 1, 2008

By Fu-Shen Zhang, Mengjun Chen, Jianxin Zhu

"In China, hazardous e-waste—cathode ray tube (CRT) glass is usually left around, and it is likely to contact with water resources directly. To identify the real leaching characteristics and bioavailabilities of heavy metals Pb and Ba contained in CRT glass in the nature environment, experiments were carried out by simulating the nature environment. The results indicated that Pb and Ba contained in CRT glass were stable in most conditions, which only showed obvious leaching toxicities in strong acidic/alkali conditions. EDTA and DTPA extractable Pb and Ba amounts were extremely high, e.g., EDTA extractable Pb of color funnel glass was up to 1960.07 ìg/kg, indicating that the potential bioavailability of waste CRT glass is very high. IntroductionIn recent years, cathode ray tube (CRT) contained monitors or TV sets has been substituted by novel and better electronic and electric equipments such as LCD and PDP, leaving huge amounts of end-of-life CRTs. 50~85% of the total weight of a computer monitor or a TV set is glass'1-21, which was classified to three categories: black & white glass (BW), color panel glass (CP) and color funnel glass (CF), according to their chemical compositions'3' (Méar et ai, 2006). In order to provide shielding from X-rays generated during the picture projection process, lead, barium and strontium oxides were used in the glass. In general, a color CRT contains 1.6-3.2 kg of lead'4'. Concerning the high toxicity of lead, these waste glasses have posed a potential risk to the environment and human health and researches on these glasses have been attracting wide and tense attention currently."

Jan 1, 2011

By R. J. Wesely

Non-ferrous smelters traditionally have a hot gas handling system. In these systems, the dust is captured as a dry material which is often recycled to the process. Some smelters use wet gas cleaning methods with the recovery of the dust as a wet sludge. Although this sludge can be recycled to the process, in some cases it is preferable to dispose of the sludge. This paper will discuss the disposal methods available and specifically will deal with one type of sludge which has a high arsenic and high lead content. Problems with this sludge were investigated and methods were tested with the aim of stabilizing the sludge so that it passes the EPA TCLP test. Results of the laboratory tests are given.

Jan 1, 2000

By Natasa Mitevska

In the world, as well as in Republic of Serbia, conventional ore reserves are almost exhausted, so the problem of their shortage is more and more expressed. On the other side, there are many locations with significant reserves of polymetallic ores which present huge potential but cannot be classically processed. Each of these classes of materials has particular mineralogical characteristics which affect their processing. Because of that it is necessary to develop particular technology for each unconventional ore in order to extract valuable elements. The aim of investigation was to define technology for complex processing of the Blagojev Kamen sulfide concentrate by pyrometallurgical procedure in order to valorize valuable non-ferrous and precious metals present, and profit with absolute respect of environmental protection laws. The complex composition of the Blagojev Kamen sulfide concentrate with high content of non-ferrous (15.59% Pb, 9.05% Zn, 2.37% Cu) and precious (697 g/t Au and 744 g/t Ag) metals was the main factor for technological procedure and collector selection. Laboratory investigations are done in four series according to technological scheme: oxidizing roasting, charge preparation (flux addition and agglomeration), smelting under reducing conditions, lead bullion refining, Dore metal refining to final products. It is concluded that precious metals are concentrated in lead bullion (up to 97.95% of gold and 93.37% of silver), which has similar composition to lead bullion produced in lead metallurgy. In this case, simplified technology is used for lead bullion processing because of low content of arsenic, bismuth, etc.

Jan 1, 2006

By Hector M. Henao

There is an increasing trend in the copper smelters to recycle electronic materials, which contain relatively high concentration of precious metals. As a consequence, the amount of precious metals lost in the slag phase is increasing. To determine the portion of the precious metals chemically dissolved and that associated with the mechanically trapped matte in the slag will be a key factor to improve the recovery of those metals. Thus, an experimental study was carried out to determine the distribution of precious metals (Au, Pt, Pd, Rh, Ru) between the equilibrated copper matte and iron-silicate slag phases. The experiments were made in a magnesia crucible at 1573 K and a fixed partial pressure of SO2 of 0.1 atm for the matte grades between 40 and 70 mass% of copper. It was found that the distribution ratios (defined as mass% X in slag/mass% X in matte, where X represents the precious metal) are around 10-2 for Ru, 10-3 for Au, Pt and Pd and 10-4 for Rh. The distribution ratios show a tendency to increase when the grade of matte is increased.

Jan 1, 2006