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By Gustavo A. Munoz

Activated carbons owe their adsorption capacities to their extensively developed pore network structure. As a result, these adsorbents generally exhibit high specific surface areas. Currently, granular activated carbons produced from coconut shells are traditionally used for gold recovery by adsorption from cyanide leaching solutions. Magnetic activated carbons (MACs) for gold recovery from cyanide solutions produced from sources other than coconut shells have been developed at the University of Utah by mixing a magnetic precursor with a carbon source, and treating the mixture under controlled conditions of temperature and gas phase composition. The pore size distribution of the activated carbons is dependent on the degree of activation, among other factors. The significance of the MAC pore size distribution on gold adsorption kinetics and gold adsorption capacity is presented.

Jan 1, 2003

By Xu Zhong

The theoretical limit to smelting rate and possibly the size of a smelter is dependent on the rate of heat transfer, and the chemical kinetics of both sulfur removal and minor element volatilization. The fundamental kinetics of volatilization of minor elements such as As, Sb, Bi, and Pb from matte and white metal is being investigated. It has been shown that the molecular form of trace elements in matte depends on the chemical potential of sulfur and the propensity for the minor element to form a sulfide. The impact of the variable molecular form of the minor elements on the volatilization kinetics is unknown and is under investigation in this study. The experimental technique is reviewed and preliminary results are reported in this manuscript.

Jan 1, 1995

By Bahram Rezai

Fine particles float poorly and less-selectively under normal flotation conditions. One of the promising methods for fine minerals is the utilization of the principle of Flocculation. Hydrophobic flocculation flotation (or floc flotation) was tested on a magnetite concentrate that was finely ground to be micron particles, for producing a concentrate with sulphur grade less than 0.1%. After that, slurry dispersing with water glass as dispersant, pyrite fines were subjected to hydrophobic flocculation induced by xanthate and a small amount of kerosene then the slurry was transferred to a flotation cell for recovering the hydrophobic flocs. The experiments carried out indicated that through one-step rougher and two-step cleaner flotation, sulphur grade was reduced from 1% to 0.1%. It has been found that the separation efficiency of the floc flotation process closely correlates with the main parameters of hydrophobic flocculation such as xanthate addition, conditioning time and kerosene addition.

Jan 1, 2006

By Tang Mo-tang

A new process for extracting indium from indium-zinc concentrates was proposed in this paper. The process can directly extract indium from removed copper solution by P204, and cancel the stage of removing iron in the traditional process because of using iron and part of zinc in the In-Zn concentrates for direct preparing high quality Mn-Zn soft magnetic ferrites. The technologies in the processes, such as leaching the neutral leached residues with high concentrated acid at high temperature, reduction ferric and removing copper, and extracting indium, were investigated. The results showed that total recovery ratio of indium has been increased from less than 70% in the traditional process to more than 95%. This process has the advantages of largely simplifying the procedure of indium extraction, zero draining off of iron residue and zero emitting of SO2. So this is a clean production process.

Jan 1, 2006

By Hiroyuki Sano

Elimination of heavy metals from the incineration fly ash by the chlorination volatilization method had been already developed and the effectiveness of this method was confirmed by the present authors. In this study, this method was applied to the elimination of heavy metals, mainly lead, from the incineration bottom ash. Since the fly ash contains a large amount of chloride, heavy metals in the fly ash are easily chlorinated. On the other hand, the addition of the chlorination agent is a key point for applying this method to the bottom ash, because it hardly contains chloride. The effects of various variables such as a kind of chlorination agent, adding quantity of it and temperature on the elimination ratio were investigated and the harmlessness of the residual ash was evaluated. The preferable condition was proposed from the recyclability of the bottom ash.

Jan 1, 2006

By V. I. Lakshmanan

Whilst the prices of metals in nominal terms have largely remained static over the past forty years, in real terms, the primary metals industry receives very much less today for its products than in the past. Yet, it has largely managed to remain competitive, despite the fact that ore reserves are not only diminishing, but are of lower grade and higher complexity, and that there are much greater pressures on companies to be good environmental stewards. This paper examines how hydrometallurgical processing has shown itself to be highly innovative in order to remain viable both economically and environmentally. Aspects of process chemistry are discussed, and the lessons to be learned from having a good understanding of this chemistry are highlighted with reference to a number of case histories such as HPAL for nickel laterites, the Avmin/Chambishi Cosac Project, use of chloride chemistry for titanium extraction, and plant effluent treatment and recycle.

Jan 1, 2003

By James A. Sommers

Combustion of niobium nitride powder in a stream of oxygen results in several niobium oxide phases, depending upon reaction parameters. Under rapid oxygen flow, the oxidation produces a molten mass which coalesces into droplets of ca. 2 mm dimension and effectively quenches to leave NbO2 and other lower oxides of niobium, despite the ambient atmosphere of oxygen. A preliminary survey of reaction parameters which govern the split between reduced and oxidized products is presented. This technique offers novel synthesis means for binary oxides when mixtures of NbN and other materials are combusted together, since the niobium moiety is generated in a molten state.

Jan 1, 1995

By Partha Patra

Extracellular bacterial protein (EBP) from Paenibacillus polymyxa was isolated. Adsorption of bacterial cells of Paenibacillus polymyxa as well as EBP onto pyrite, galena and sphalerite was studied. Both bacterial cells and EBP was found to have different adsorption density for different minerals. Protein from mineral surfaces were extrated and examined through SDS PAGE electrophoresis. Specific group of protein was found to be adsorbing, specific to respective minerals. EBP was fractionated through FPLC. Adsorption studies were carried out with each fractions. Difference in adsorption density was observed for individual minerals. Flocculation and flotation experiment were carried out with these mineral specific EBP. Pyrite was selectively removed from ternary mixture of galena and spharite through flocculation anf flotation using pyrite specific EBP. Mineral specific EBP was found to selectively separated remove pyrite from the complex sulphide mixture.Zetapotential studies were carried out to examine the surface chemical changes of the minerals on interaction with EBP. Hydrophobicity of the minerals were carried out on interaction with bacterial cells as well as mineral specific EBP.

Jan 1, 2006

A full-scale test of chalcocite heap bioleaching was undertaken at Straits? Nifty Copper Operation. Straits worked closely with the CSIRO to investigate the chemical and biological changes over the life cycle of this chalcocite heap bioleach system. Results indicated nearly 80% copper recovery was achieved in just over 300 days. Significant changes in iron chemistry and microbiological activity were detected. Temperatures in the heap reached as high as 70 ºC during the time of maximal copper recovery rate. The dominant cultivatable bacterial strains were typical mesophilic bacteria, however, naturally occurring moderately thermophilic bacteria were detected by culture and culture independent molecular (PCR followed by denaturing gradient electrophoresis [DGGE]) and signature lipid methods. Signatures for the iron and sulfur-oxidising species Acidithiobacillus ferrooxidans and Sulfobacillus spp., as well as the moderately thermophilic heterotroph Alicyclobacillus sp. were detected. Biomass was greatest in ?warm? but not ?hot? parts of the heap, and Hyperthermophilic Archaea were not detected.

Jan 1, 2003

By Mark L. Dietz

The unique physicochemical properties of room-temperature ionic liquids (RTILs) have led to intense interest in these materials as alternatives to conventional organic solvents in a range of synthetic, catalytic, and electrochemical applications. Recently, there has been growing interest in their potential use in various separation processes, among them the liquid-liquid extraction of metal ions. Although certain RTIL-extractant combinations (e.g., crown ethers in 1-alkyl-3-methylimidazolium bis[(trifluoromethylsulfonyl] imides) have been shown to provide extraction efficiencies far exceeding those observed with conventional solvents, recent work suggests that the utility of RTILs may be limited by solubilization losses and difficulties in recovering extracted metal ions. In this work, we demonstrate that these limitations arise, in part, from differences in the mechanism of metal ion partitioning in RTIL systems versus conventional organic diluents and consider approaches by which they might be overcome.

Jan 1, 2003

By Javier Antoñanzas, Juan Carlos Múgica, Lourdes Yurramendi

The gasification of wastes containing an organic fraction is usually performed at low-medium temperature using different kind of catalysts. The off gas obtained is a mixture of carbon oxides, mainly carbon monoxide, and hydrogen and can be used for different energetic applications. The main problem is the production of tars in the off gas that has to be separated from the valuable gas flow and, finally, treated separately. An interesting alternative is the partial or total treatment of organics at high temperature. In this case, the off gas contains a higher content of hydrogen and elemental carbon as particulate matter. The energetic source to obtain a temperature in the range of 1,000 - 1,200 ºC is obtained by a plasma torch. In order to make de process attractive, an important issue to be considered is to commercialize the carbon obtained for different industrial applications.

Jan 1, 2008

By Tian Li

Molecular crystal growth during gibbsite precipitation from caustic aluminate solutions under different flow regimes was investigated in three different laboratory precipitators. The gibbsite precipitation experiments were conducted at the same temperature, initial liquor composition and seed type. The Taylor-Couette precipitator and the stirred tank precipitator were operated, respectively, under the laminar and turbulent flow regimes, while the bottle roller precipitator was operated in a complex flow regime, where fluid flows are generated by the end-over-end rotation of the bottles. Comparison of the growth rate estimates from the different flow regimes showed good agreement, which suggests that the hydrodynamic regime has little or no effect on gibbsite crystal growth under the operating conditions employed in this work. The growth rate estimates from the current precipitation study showed a second order dependency on supersaturation and is consistent with a screw dislocation growth mechanism. The findings of the current work are in agreement with previous gibbsite crystal growth studies published in the literature.

Jan 1, 2003

By Byung-Su Kim

Most electric arc furnace dust (EAFD) treatment processes employ carbon as a reducing agent for the zinc oxide in the EAFD. In the present work, the reduction reaction of zinc oxide with carbon in the present of various additives was studied. The effects of temperature and the additives of calcium carbonate, magnetite, and mill scale on the kinetics of the reduction reaction were measured in the temperature range of 1173 K - 1373 K under nitrogen atmosphere using a weight-loss technique. The mill scale is one of byproducts generated from the steel rolling process. From the experimental results, it was concluded that all three additives accelerates the reaction rate of zinc oxide with carbon, but the effect of addition of calcium carbonate is the highest. It was also found that magnetite, mill scale, and calcium carbonate in the reduction reaction of zinc oxide with carbon promotes the carbon gasification reaction.

Jan 1, 2006

By María Cristina Ruiz

In the processing of copper concentrates by the conventional smelting-converting technology, complying with the increasingly severity of environmental legislation in some countries has become difficult, mainly due to severe fugitive emissions of gases produced during the batch PS (Peirce-Smith) converting step. In this work, the results of an investigation on the pressure leaching with sulfuric acid and oxygen of white metal (produced in a Teniente Converter reactor) are discussed. The study was carried out at laboratory scale and the main variables studied were temperature, concentration of sulfuric acid and partial pressure of oxygen. The experimental results indicated that most of the sulfur in the white metal was oxidized to sulfate in the whole range of temperature studied (105ºC to 150 ºC). The concentration of sulfuric acid over 0.05 M, and oxygen partial pressure over 6 atm had little effect on the dissolution of copper from the white metal. On the other hand, temperature had the most significant effect on copper dissolution; below 130 ºC copper dissolution was incomplete after 5 hours of leaching while at 150 ºC the dissolution was complete in 90 minutes and 10 atm of partial pressure of oxygen

Jan 1, 2006

By Daniel Helm

The first industrial application of direct solvent extraction of nickel from hypersaline sulfate feed solutions has highlighted the need to investigate the influence of chloride on the extraction behaviour nickel in the presence of calcium using Versatic 10 and the solubility characteristics of gypsum. Temperature-solubility curves for gypsum in various aqueous electrolytes were prepared. The solubility of gypsum is increased significantly by the presence of sulfate ions, while chloride ions decrease it for a given temperature. The anion effects of chloride and sulfate on the extraction of calcium and nickel by Versatic 10 corresponded well with the complexing ability of the anions. It was shown that the presence of chloride shifts the extraction isotherms for both metals significantly to the left, while decreasing the selectivity of Versatic 10 for nickel over calcium. The loading of nickel onto Versatic 10 in this system was shown to be at a maximum within 3 seconds, while calcium extraction took between 4 ? 5 seconds to load to a maximum. Chloride ions had no influence on loading kinetics of nickel, but depressed the rate of calcium loading. It was shown that in the presence of an excess of nickel, calcium loading is effectively eliminated, and that calcium is scrubbed from Versatic 10 within 2.5 seconds of contact with nickel electrolyte.

Jan 1, 2003

By S. K. Kawatra

A growing concern for pyrometallurgical operations is the generation of airborne particulates. These particulates can be generated by combustion processes, or by materials handling. Regulation of these particles by the EPA has become progressively more stringent, first for particulates finer than 10 micrometers (PM10), which are particles fine enough to be inhaled into the lungs. Then, restrictions were introduced on emissions of particles finer than 2.5 micrometers (PM2.5), which are fine enough to become embedded in lung tissues. The next stage of regulations is likely to be ?nanoparticulates,? particles finer than 100 nanometers, which are in a size range where their very high surface area leads to enhanced reactivity. While all of the health effects due to nanoparticulates have not yet been determined, there have been enough studies to indicate that there is a problem, and restrictions on nanoparticulate emissions are only a matter of time. In this paper, it will be demonstrated that dry handling, comminution, and combustion sources represent a significant concern for both PM and nanoparticulate emissions. In regards to dry handling, the effects of utilizing effective dust suppressants on PM and nanoparticulate emissions will be explored.

Jan 1, 2006

By Ahmet Geveci

[Generally accepted formula related to sulfur slag-metal distribution ratio is given by the following equation: [ ] According to the above equation it can be deduced that sulfur distribution between slag and metal is governed mainly by metal composition (?s term), slag composition (slag basicity and in turn sulfide capacity), oxygen potential of the system (ao¬¬ term) and temperature(related to equilibrium constant, K). In this study, the results of ladle furnace operations conducted in Erdemir-Iron and Steel Works Co. (Turkey) in relation to sulfur removal, have been given. Typical ladle furnace slag analyses of 4937K quality steel have been presented. Activity coefficient of FetO,?FetO, have been calculated with the relation obtained fromthe literature. Activity calculations have been performed with the program written in Mathcad. The changes in activity of aFetO in the slag phase,, have also been studied in relation to the sulfur removal: The relation between % Decrease aFetO and %DeS (measured)have been investigated for 4937K runs and someother types of steel produced in the Erdemir Plant. Related to ladle operations %desulfurization defined as [(%Sinitial-%Sfinal)/S%initial]*100 values have been presented for different steel qualities.]

Jan 1, 2006

By Tiffany Brown

In the thiosulfate gold leaching process, thiosulfate is used to complex gold following electrocatalytic oxidation of the native metal by Cu(II)-ammines. Unfortunately, Cu(II) complexes also catalyse the undesirable conversion of thiosulfate to polythionates. We have been seeking alternatives to ammonia, which fulfil the role of ammonia but minimize thiosulfate decomposition. One aspect of these studies has involved the determination of the rate of thiosulfate oxidation by the Cu(II) complexes from UV-Visible spectral changes. Various ligand classes, including pyridyls, polyamines, aminocarboxylates and picolinates, have been tested and the majority found to inhibit thiosulfate decomposition. Interesting variations in reactivity with the nature and denticity of the ligand and L/M ratio have been observed. In the case of open chain polyamine ligands with 2 to 5 nitrogen donors, the rate of thiosulfate oxidation was generally found to decrease with the denticity and the concentration of each ligand. Saturation of the Cu(II) coordination sphere appears to inhibit the oxidation of thiosulfate when excess thiosulfate is present. The Cu(II) complex of the branched polyamine ligand, tris(2-aminoethyl)amine (tren) exhibits this behaviour in excess thiosulfate. Interestingly, when the [Cu(tren)(OH2)]2+ complex is in excess oxidation of thiosulfate was observed. This unexpected finding prompted a spectrophotometric study of this reaction which has revealed that the oxidation of thiosulfate involves several processes, two of which involve the formation and decay of a tetrathionate radical.

Jan 1, 2003

By M. I. Kalashnikova

The leaching of metal nickel in copper sulfate solutions is investigated. It is established, that irre-spective of presence or absence of chloride-ion and oxidizer (oxygen) in system process can be divided into three stages, characterizing by restoration and oxidation of metals with formation of metal copper and cuprite and differing in the speeds of sedimentation of copper and transition of nickel into solution. At the initial stage of process along with allocation of metal copper it is be-sieged cuprite, that results in excess of speed of sedimentation of copper in comparison with dis-solution of nickel. At the second stage speed of transition of nickel into solution falls practically to zero, and sedimentation of copper proceeds on reaction of interaction of metal copper with copper sulfate solutions with cuprite formation. During the final period speed of transition of nickel into solution exceeds speed of sedimentation of copper due to course of reaction of resto-ration of cuprite up to metal. Influence of an ion of chloride and oxidizer on formation of various phases is revealed. It is established, that presence of an oxidizer results in increase in a share of cuprite in a deposit. With increase of the maintenance of chloride-ion speed of metal copper allo-cation essentially grows even at presence of an oxidizer in system.

Jan 1, 2006

By Thomas K. Chow

For the well-being of all living creatures and in response to green-environment policy from governments around the global, it is essential to reduce SO2 emissions from mining / smelters as well as other industrial facilities around the globe. However, often times, these SO2 containing flue gases and smelter flash gases also include oxygen and SO3, which complicate the SO2 removal process and technology. There are many novel technologies recently developed for removing SO2 from such gases. Most of these, however, have not yet commercially demonstrated that they are technically viable and economically feasible. Many of these novel processes also generate undesired byproducts, which themselves then need to be disposed of in a safe and cost effective manner. Fluor has developed the Fluor SOx Cleanup Process with a wide variety of process configurations to customize removal of the undesired flue gas constituents in a cost-effective manner. The process removes practically all SO2 in the form of salable elemental sulfur and also reduces CO emissions. Successful operation of major components of the Fluor SOx removal technologies has been demonstrated in many commercially operating units. Besides their technical viability and economic feasibility, Fluor SOx removal technologies do not generate any undesired byproducts or encounter SO2 associated corrosion issues. Moreover, these technologies produce high-purity, saleable elemental sulfur. This paper discusses the merits of the Fluor SOx removal technologies, their technical and cost advantages, their simplicity in design and operation, and their readiness for implementation.

Jan 1, 2006