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By Laurence G. Dyer, David G. Dixon, John Rumball, Maziar Eghbalnia, Edouard Asselin

"Linear scan voltarnmetry was used to determine the reactions that occur during the cyanidation of petzite (Ag3AuTe2). Gold oxidation in petzite requires more oxidising conditions than are required for pure gold, it also does not achieve the same current (related to reaction rate). Tellurium oxidation occurs at a similar potential in water and cyanide, but as a component of petzite is impeded somewhat in water, likely due to the stability of the precious metals. Pre-treatment of petzite to oxidise tellurium in the absence of cyanide prior to gold recovery appears to be at least moderately successful.IntroductionWhile gold occurs most prevalently in its native form, many other gold bearing phases appear throughout natural systems [I]. Tellurides are a common group of such minerals, many of which also contain silver, often existing in association with native gold deposits. The six major gold-bearing tellurides are calaverite (AuTe2), sylvanite [(Au, Ag)2Te4], montbrayite [(AuSb)zTe3], krennerite [(Au1-x, Ag,)Te2], petzite (Ag3AuTe2) and muthmannite (AuAgTe2) [2]. While several other phases exist they are much more complex (i .e. buckhornite), which dilutes and confuses the influence of each specific component. Studies of gold tellurides have predominantly focussed on calaverite as it is the simplest and most common phase, however petzite, commonly found in Australia and North America, is the focus of this investigation.Gold processing via cyanidation has been operated for more than a century and is a highly effective hydrometallurgical treatment of native gold deposits. However, some gold alloys such as tellurides have proven to be somewhat less responsive under the same conditions. Several groups have shown that gold/silver tellurides are amenable to cyanidation, but are significantly more refractory than native gold [3]. Pre-oxidation steps have been tested to remove constituents that would consume cyanide such as sulfides. Such species are also linked to the precipitation of oxidised telluriwn, forming a passive layer, further inhibiting gold recovery [2]. It is uncertain to the definite reasons underpinning the refractory nature of precious metal tellurides in conventional cyanidation."

Jan 1, 2012

By G. T. Lapidus, O. J. Solis-Marcial

"The oxidative dissolution of copper from refractory minerals, such as chalcopynte, represents a technological challenge that has occupied hydrometallurgists for more than half a century. Innumerable processes have been suggested, but the majority operates at high temperatures or employs corrosive media. The origin of this refractory nature is the formation of passivating phases of iron(III) or copper. One option is to add non-corrosive ligands that complex these metal ions, thereby facilitating their dissolution. In the present work, the effect of acetone in sulfuric acid solutions was studied. The initial experiments were on chalcopynte carbon paste electrodes using cyclic voltammetry, where greater reactivity was observed. Later, leaching tests with hydrogen peroxide, cupric sulfate and ozone and, as oxidants, were performed. High extractions were achieved in three hours at 50°C. The solid residues contained the iron in the form of Fe203 and FeOOH.IntroductionChalcopyrite is the most important mineral of polysulfide copper ores [1] and accounts for approximately 70% of the world's copper reserves [2]. Currently, the copper present in chalcopyrite is extracted mainly by pyrometallurgical processes, which generate environmental concerns because of the formation of SO2 gas and submicron particulates [3]. The development of a less aggressive hydrometallurgical process for the extraction of copper would constitute a possible solution to these problems. For that reason, studies of the dissolution behavior of chalcopyrite are of great technological importance [4], However, the proposed oxidative leaching routes for chalcopyrite, generally at high pressures and temperatures, have not been implemented on an industrial scale, because of the elevated costs required to equal the high copper extractions obtained in thermal processes. These extreme leaching conditions are required because of the refractory nature of chalcopyrite. Passivation has been used to explain this phenomenon, although researchers have disagreed on the composition of the layer, which is various have assumed to be sulfur, copper sulfides, and iron-bearing jarosites or hydroxides [5]. If the latter compounds are the cause, an alternative solution would be the use of polar organic solvents in the oxidative leach to decrease the formation of the passivating iron layer. In this work, the influence of acetone on the oxidative leaching of a chalcopyrite concentrate at room conditions is explored."

Jan 1, 2012

By Jiann-Yang Hwang

Hydrogen storage is a critical issue for the hydrogen economy. Current storage technologies are not able to meet the combined gravimetric, volumetric, and system cost targets set by the Department of Energy. To solve the problem, the development of a new material - perhydride ? is proposed. Perhydrides are defined as materials that contain more hydrogen atoms in their molecules than conventional hydrides do based on the valence. This concept is supported by the versatile bonding capability of hydrogen and the recent discoveries in the chemistry of hydrogen clusters.

Jan 1, 2006

By Shirley Cosin, Guillermo R. Martín-Cortés, Francisco R. Valenzuela-Díaz, Jorge E. Di Rito, Valquiria F. J. Kozievitch

"A procedure that is being studied as a potential method for correct disposal of industrial wastes by incorporation on common clay bodies in the fabrication of structural ceramic products as bricks, blocks and roof tiles. The objective of this paper is to present the results obtained with mixtures of unburned sanitary ware wastes with a common clay from Jundiai, São Paulo, Brazil. Preliminary tests of incorporation (1,0% to 30,0% in weight) were made with hand formed spherical test bodies. With the proportion that presented spheres with the higher compression strength after drying and after firing (950°C) prismatic samples were extruded. Based on the ceramic properties of those mixtures an industrial test was performed. Six hundred hallow blocks containing 30% waste were fabricated and presented ceramic properties similar to those without incorporation. Introduction The sanitary ware segment has a very great prominence in South America, placing Brazil as one of the greater producers of the world.. Inside the country, the city of Jundiai, in the State of São Paulo is the greater producer region of this ware. Great part of the material is destined to exportation and daily it is produced high number parts. High exportation requirements make that the amount of powder waste rejects reach astronomical volumes. Until the moment too small part of that material it is re-taken with advantage, because in the own segment, there is not an economic viability, by the fact of the exigencies concerning the quality of the final product [1]. If from one side it exists that material that at the moment is deposited in landfills, or stored at the patio’s factories, from the other side the exigency of adopting exploitation rules, recycling and obedience to Laws relative to the environment as ABNT 10400, therefore it is a material that if well studied, it will certainty have a noble destiny [1]."

Jan 1, 2008

By T. T. Chen

This mineralogical study is based on samples from typical "wet" nickel laterites of humid tropical to sub-tropical regions. An in-situ nickel laterite sample from Goro and a transported laterite sample from Plaine des Lacs, New Caledonia, are predominantly limonitic. Two-thirds of the particles in the Goro sample are <10 um in size; they consist of skeletal goethite and serpentine, as well as minor amounts of talc, gibbsite, chlorite, quartz and clay minerals. The coarser grains are mainly Cr-spinel, serpentine, gibbsite and Mn oxide. Nickel occurs mainly in goethite, serpentine and Mn oxide; cobalt occurs in goethite and Mn oxide. The Plaine des Lacs sample is finer-grained and contains more Al and CO3, but less Mg and Si than the Goro material. The sample contains more kaolinite, chlorite, siderite and feldspar, but less serpentine and gibbsite than the Goro material. Nickel is detected mainly in goethite, serpentine, Fe-Mg silicate and Fe-Mn oxide. The Indonesian ore from Sorowako, as sampled from the reduction kiln feed containing some reverts, is predominantly saprolitic, with apparent particle sizes ranging from <100 um to > 1 cm. The sample of reduction kiln feed is rich in Mg silicates, Mg-Fe silicates and goethite, and exhibits complex alteration textures. The nickel contents vary from particle to particle. Nickel is present mainly in serpentine, olivine, chlorite and amphibole, and in subordinate amounts in goethite and Mn oxide. Cobalt is detected in the Mn oxide. Keywords: Nickel Laterite; Mineralogy; Nickel Carriers; Goro, New Caledonia; Plaine des Lacs, New Caledonia; PT Inco., Sorowaki, Indonesia

Jan 1, 2004

By Nozomu Uchida, Uematsu Keizo, Daisuke Shouji

"Grain orientated microstructure was developed for the improvement of ceramic characteristics. Novel polarized light microscopy was developed to examine the grain orientation quantitatively. The degree of grain orientation was estimated from the retardation determined with a Berek compensator. The method was essential to determine a minor grain orientation, which could not be analyzed by means of conventional X-ray measurements. The data were favorably related to ceramics characteristics. The comparis of the ceramics with various degree of orientation was very important to explain the change of ceramic characteristics with processing.IntroductionMicrostructure with grain orientation has a high potential for greatly improving characteristics of ceramic. However, there has been strong restriction on processing and material for developing this structure. It has been crucial to apply forming methods involving high shear such as injection molding1). Grains must have an elongated shape.In recent years, much attention has been paid on the effect of high magnetic field on diamagnetic materials2)3)4), Many ceramic materials are known to be diamagnetic. High magnetic field has a high potential to orient grains. The principal driving force for grain orientation is the magnetic anisotropy of material, which is generated by non-cubic crystal symmetr5). This method of grain orientation is not restricted by grain shape, and can be applied to all materials having non-cubic crystal structure.This study uses alumina as raw materials, and produces alumina ceramics with orientated grain in high magnetic field (10T). Alumina has a magnetic anisotropy due to hexagonal crystal structure. The degree of grain orientation in the green and sintered bodies will be examined and their relevance to magnetic field will be discussed."

Jan 1, 2000

By E. Gervais

Modern life in inconceivable without zinc. Zinc provides the most cost-effective and environmentally efficient method of protecting steel from corrosion. Zinc is also used to power electric vehicles and computers, to make brass, automotive equipment, household appliances, fittings, tools and toys, and to support the building and construction industries. It is also used in pharmaceuticals and cosmetics, in rubber, in fertilisers and in animal feeds. The links between properties, applications and performance, as well as zinc demand and market dynamics, will be reviewed along with market development opportunities and successes. The presentation will also include a progress report on the five-year plan of the International Zinc Association to increase the global market for zinc, over and above the natural growth, by 500,000 tonnes/year by 2002.

Jan 1, 2000

By R. C. Hubli

A panial equilibrium model? to simulate the dissolution of millerite (NiS) in aqueous solutions containing copper(II) chloride as the oxidizing species has been developed. The predominant copper(I) and copper(II) species are CuQ3 and CUO2 respectively. The model computes the initial concentrations of the species present in the aqueous phase under the specified input conditions, prior to the simulation of dissolution. During the dissolution of millerite, nickel enters the leach liquor as NiH and it has been found that the H+ decreases as a function of NiS dissolution. The simulation has been accomplished under conditions prevailing during actual dissolution, with only one mineral undergoing dissolution. The model can be applied for the simulation of co-dissolution of two or more sulfides. Under the given conditions, the precipitation of Cu1(OH»)O is negligible but loss of Cu(1l) could be significant if the initial H+ is lower than 0.03 M. The results of the simulation compare favorably with experimental observations.

Jan 1, 1996

By Lichao Ding, Chunhua Liu, Yunnen Chen

"In this paper the simulated acid magenta dye discoloring the reaction process was researched. The results showed that it attained highest decolorization efficiency for acidic magenta simulation dye wastewater when pH 9 and reaction time 10 min. With the initial dye wastewater concentration increased, the decolored rate decreased. The decolored rate in general kept a tendency to increase with the temperature increased. Kinetics researches showed that when pH 9, reaction temperature 20 and 35 ?, the decoloring reaction process for the dyes accorded with the First-order dynamic equation. The decoloring reaction rate constant was influenced by initial concentration of dye wastewater and temperature.1. IntroductionIn China, textile printing and dyeing industry is one of industrial departments which using more water and discharging more wastewater. There is about 7 billion tons of waste water discharge each year, of which 80% from the process of printing and dyeing. Being complex ingredients, high chroma, more toxic substances and severe environment pollution, the treatment of printing and dyeing wastewater becomes problem urgent to be resolved. The traditional treatment methods such as adsorption [1], coagulation [2], biochemical method [3,4], which has advantages of simple equipment, simple operation and mature process, but they can cause waste accumulation and secondary pollution [5,6].Magenta is a kind of organic compounds, which classified into acid and alkaline magenta. Considering the advantages of simple operation, low cost, simple experiment equipment and friendly to environment, acid magenta dyes wastewater was chose as object in this paper. Some parameters such as pH, contact time, temperature and the initial concentration on of simulative acid magenta dyes wastewater were studied."

Jan 1, 2012

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 Yanxia Lu

Porous silicon carbide (SiC) has been the top selection for diesel particular filters (DPFs) since 2000 because of its high thermal diffusivity and strong body, which help it to survive in the harsh environment of a diesel exhaust system. However, the process to produce SiC DPFs is a costly one. The work presented herein describes more cost effective composite materials for this application, namely Si-SiC and Si₃N₄-SiC. Both composites have shown excellent filtration efficiency, low back pressure and outstanding survivability of regeneration at high soot loadings. Since the composites are batched from silicon metal, they can be prepared by a low temperature process that is impossible in the production of pure SiC PDFs. In fact, fabrication of SiC composites simply involves reactions between nitrogen gas and silicon metal, or silicon metal bonded with SiC, and as such uses a much less costly process when compared to the one employed to make SiC. In addition, the pore structure of the composites can easily be tuned by selecting raw materials and changing the ratio of two components. A typical pore structure consists of well connected pores with a median pore size of 5-20 µm and a porosity of 40-55%. This talk will describe the exothermic behavior as well as the mechanical and thermal properties of SiC composites in comparison to those of SiC filters. It will also show the superior thermal shock resistance of Si₃N₄ bonded SiC which is due to the unique combination of these phases that lowers the thermal expansion and elastic modulus relative to pure SiC.

Jan 1, 2006

By J. G. Peacey, P. Hancock, R. -Q. Li

A pyrometallurgical process for the direct recovery of zinc from zinc concentrates and zinc/iron residues has been proposed and tested extensively by Noranda. The process consists of smelting bone-dry zinc containing materials (sulfide concentrates and secondary zinc/iron materials) in a molten iron oxysulfide bath to volatilize metallic zinc into a SC^-free offgas. Sulfur contained in the feed materials is fixed as an iron oxysulfide matte for disposal. Thus, this process not only is capable of treating zinc sulfide concentrates and secondary zinc materials simultaneously, but also eliminates the need of sulfuric acid production. Detailed thermodynamic analysis and experimental test work are described in this paper.

Jan 1, 2000

By Jeong-Hwan Kim

The liquid-liquid reactive process (solution process) is often adopted as a synthetic method for precipitated calcium carbonate (PCC) in laboratory studies for its simplicity in operation or ease in controlling process variables. Still, PCC are produced commercially by passing carbon dioxide through a milk of lime, i.e., by a gas-liquid reacting method (carbonation process). Few studies on the carbonation process have been conducted, since the process variables are interrelated and difficult to control compared to the solution process. In this study, both carbonation and solution processes were employed to study the polymorphs of calcium carbonate and growth rate of PCC crystals. The effects of the characteristics of limestone ores as a raw material in the synthetic system of PCC on the synthetic characteristics of PCC were also investigated. To control the nucleation rate in the synthetic systems, the shape factor was considered most important. Single-phase aragonite PCC could be synthesized under a variety of controlled experimental conditions such as ionic strength, solution composition, concentrations of additive ions, and temperature.

Jan 1, 2006

By Patrick R. Taylor

The synthesis of high-purity ultra-fine barium strontium titanate powders (BST: BaO6Sro.4TiO3) has been performed in a non-transferred are D.C. thermal plasma reactor. Slurries of aqueous solutions of dissolved barium and strontium nitrates and solid titanium dioxide powders were used as precursors. Oxygen and argon were used as carrier gases, and pure argon and combinations of argon and nitrogen were used as plasma gases. The plasma torch power was varied, as well as the oxygen flow rate and the total molar concentration of the precursors. A graphite plate was designed to protect the torch electrode and lower the level of impurities in the product. A thermochemical analysis of the Ba(NO3)2-Sr(NO3)2-TiO2-H2O-O2 system was performed to predict the conditions for the formation of BST and the feasibility of the reaction, The powders collected from the different sections of the reactor were characterized using Transmission and Scanning Electron Microscopy, X-Ray Diffraction, and ICP chemical analysis. The powders produced showed high conversion to BST, ultra-fine particle size (< 30 rim) and high purity, which makes this a potential process to produce ceramic materials for electronic devices.

Jan 1, 2003

By G. Riverin, C. Simard, W. D. Stevens

"An on-line technique to measure the efficiency of decoating I delacquering processes is being developed by Alcan' s Arvida R & D Centre. Decoating processes are used to remove moisture and coatings from shredded coated material such as Used Beverage Containers (UBC) before melting. Complete removal has been demonstrated to maximize metal recovery. Quantifying the weight of carbon and organic residue adhering to the shred surfaces is very difficult to measure directly, as the material can be highly folded. The technique developed indirectly measures the residue remaining by analysing the concentration of CO evolved in the decoater end zone exhaust gas.A commercial CEMS (Continuous Emission Monitoring System) incorporating an infrared type CO gas analyser was modified for on-line process exhaust gas analysis. Both pilot and plant trials had demonstrated that the CO concentration measured was inversely proportional to the efficiency of the organic removal achieved. As the quality of coated purchased scrap can be highly variable in moisture and organic content, continuous measurement should permit adjusting the feed rate and other decoater process parameters to the quality of decoating required."

Jan 1, 2000

By Herbert Pöllmann

Waste disposals are needed for safe deposition of different kinds of materials which can not be used as secondary raw materials. Often high contents of heavy metals must be bonded tightly to cristalline compounds to protect the environment from contamination. Therefore it is important. to find minerals which are capable to incorporate different heavy metals and protect the ground water. The power of resistance against leaching out effects of highly water-soluble salts can be increased. Mineral groups of metal hydroxy salts, ettringites, apatites, sodalites and calciumchlorosilicates and their hydrates are recommended for their formation in mineral reservoirs. Different wastes as red mud, gasification ash, garbage combustion ash and fluidized bed ashes were included in this study. The formation of different new compounds and their properties were determined.

Jan 1, 1991

By William Petruk

The behaviour of sphalerite during mineral beneficiation of base metal ores has been studied at CANMET and other institutes for at least 15 years by determining the liberations of sphalerite in mill products and calculating the recoveries of liberated and unliberated sphalerite in zinc concentrates. Sphalerite in base metal ores commonly occurs as layers and as interstitial material between pyrite. Layered sphalerite is generally liberated during primary grinding, but interstitial sphalerite requires re-grinding to achieve liberation. Around 95% of liberated sphalerite is generally recovered in zinc concentrates frau zinc circuit feeds. A series of tests was conducted on sphalerite in the ore of Brunswick Mining and smelting during a continuous fine tuning operation of the concentrator. It was found that a grind of 80% minus 37 micrometres was required to liberate the interstitial sphalerite. The fine grind increased Zn recoveries from 75% to 78-80%, but produced liberated slimed sphalerite which was lost. Since regrinding to a fine grain size is needed to obtain the desired sphalerite liberation, a method of recovering the slimed sphalerite is required.

Jan 1, 1990

By Rzyman Michal, Nakamura Takashi, Shibata Etsuro, Grabda Mariusz, Oleszek-Kudlak Sylwia

"Tetrabromobisphenol A (TBBPA) and many systems based on the synergistic effect of brominated organic compounds with Sb2O3 are extensively used as effective brominated flame retardants (BFRs) in many materials such as plastics and textiles. Thermal degradation of BFR containing plastics leads to the formation of hydrocarbons and gaseous compounds such as HBr and SbBr3. Our thermodynamic considerations indicate that these gases can act as bromination agents for metallic oxides such as ZnO, Cu2O, CuO, PbO and FeO. Moreover, these metallic oxides have the thermodynamic tendency to brominate easier than does Sb2O3. The aim of this study was to investigate experimentally the reactivity of ZnO with 1) HBr originating from the thermal decomposition of TBBPA and 2) SbBr3, which is formed during thermal degradation of brominated flame retardant plastics. The thermal treatments of the mixture of compounds of interest were investigated by thermogravimetry coupled with mass spectrometry.IntroductionTetrabromobisphenol A (TBBPA) and many systems based on the synergistic effect of brominated organic compounds with Sb2O3 are extensively used as effective brominated flame retardants (BFRs) in materials such as plastics and textiles. For instance, 4.5 million tons of flame retardant plastics containing BFRs are produced in Japan each year. Thus, in thermal treatments such as the incineration and melting of solid wastes, BFR containing plastics are intentionally or unintentionally included in the wastes. Thermal degradation of BFR-containing plastics leads to the formation of hydrocarbons and gaseous compounds such as HBr and SbBr3 [1-5]. Our thermodynamic considerations [6] indicate that heavy metal oxides such as ZnO, Cu2O, CuO, PbO and FeO should easily react with HBr prior to Sb2O3 and also with SbBr3, the main gaseous product in the thermal decomposition of TBBPA, forming low boiling point metallic bromides suitable for the volatile separation of heavy metals. The metal oxides are also expected to qualitatively and quantitatively affect debromination and decomposition of the flame retardant."

Jan 1, 2008

By Akram Alfantzai, Farzad Mohammadi, Maysam Mohammadi

"Degradation of lead anodes has always been a major concern among the electrowinning industries. In this study, the effect of agitation of the zinc electrowinning solution on the integrity of lead anodes was investigated. Galvanostatic experiments were performed at 37±0.5°C using 0,600 and l000rpm magnetic stirring rates for 24 hours. The Pb02 layer formed on the anode surface was reduced to PbS04 (discharged). The discharge information was used to calculate the amount of Pb02 present on the surface. Weight loss measurements along with the discharge calculations revealed that the degradation rate of the lead anode increased as the solution was stirred more vigorously. Furthermore, the amount of remaining Pb02 on the surfaces was decreased as a function of solution velocity. Therefore, it may be concluded that, degradation rate oflead anodes is controlled by detachment of the corrosion products from the surface rather than by electrochemical reactions. IntroductionElectrowinning is one of the extraction stages of zinc, in which pure zinc is deposited from acidic solution after froth flotation, roasting and leaching processes. The anode electrode materials play important roles in the electrowinning process. Their electrocatalytical capacities determine the oxygen evolution overpotential, and consequently the cell potential and energy efficiency of the zinc electrodeposition [l]. Purity of the zinc deposited on the cathode is affected by the solubility and corrosion resistance of the anode materials. Using insoluble materials as anode in the electrowinning leads to the higher purity of the deposited metal on the cathode[2]. Lead (Pb) and its alloys have been used as the anode in the zinc electrowinning because of its special properties such as relatively low cost, low melting point, insolubility in solutions containing sulphuric acid and high conductivity in both states of metallic and oxidized [3, 4]. In zinc electrowinnig, zinc reduction occurs on the cathode (reaction 1) and the oxygen evolution reaction (OER) (reaction 2) is the main anodic reaction [5, 6]."

Jan 1, 2013

By Hua-qing Li

Electromagnetic stirring process effectively improves the casting quality of metals. In this paper, the physical simulation experiment, in which the molten copper is displaced by mercury, was designed. The factory test parameters were determined according the simulated data. The flow behavior of the mercury to be stirred as well as the relations between the microstructure of plate blanks and the current parameters were analyzed. With an appropriate electromagnetic stirring, the inverse segregation of tin for C51900 alloy plant blank reduces from 15 % ~ 30 % to about 5 %, and the proportion of equiaxed grain rises to larger than 30%.

Jan 1, 2009