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By Denise Corrêa de Oliveira

Household zinc based batteries, dry and alkaline, has become the most popular sources of electrical energy, and are widely used. Because of their heavy metals content such as mercury, zinc and manganese, spent batteries cannot be directly placed in common landfills without a pretreatment. As a municipal solid waste, these batteries may cause serious health problems and environmental impacts. These damages can be reduced by recovery (which means saving natural sources and energy), recycling and adoption of cleaner technologies. Although this worry has been increasing recently, and producers are doing efforts to reduce the mercury content, batteries still need proper safe disposal conditions or recycling processes. This work presents the efforts in progress to characterize and recycle mixed - dry and alkaline - spent batteries, by using low cost unit operations. Some possible recycling stages and recovery parameters of metals as zinc and manganese are also discussed.

Jan 1, 2001

By Wenjie Zhu

Hexavalent chromium is a widespread environmental contaminant. An Achromobacter sp. strain nominated Ch1 can reduce soluble and toxic chromate to insoluble and non toxic Cr(III) in aerobic cultures, and no Cr(VI) decrease was observed in anaerobic cultures. In contrast with other Cr(VI) reducing microorganisms, Ch1 showed higher Cr(VI) reduction at high pH. Reduction performed under alkaline conditions at pH 7 to 11, and the optimal pH was 10. During the reduction, pH decrease was observed may caused by production of acidic metabolic byproducts from aerobic respiration. In the present study, the ability of Achromobacter sp. Ch1 to reduce Cr(VI) during growth was evaluated with lactate as an electron donor. In NB medium, Ch1 reduced 100% of 24mM of Cr(VI) in 35h, but only 73% of 30mM of Cr(VI) after 48h of inoculation. Reduction was inhibited by metal ions like Ag+, Cu2+, Zn2+, slightly inhibited by Mn2+, and not affected by Mg2+. Results revealed that reduction rate of Cr(VI) also increased with the increasing of concentrations of lactate, and complete reduction was achieved at the concentrations above 40 mM. HPLC analysis demonstrated Cr(VI) reduction was associated with the consumption of lactate. There was a large quantity of dark blue sediment generated in the culture during Cr(VI) reduction by Ch1. Energy dispersive X-ray (EDX) analysis showed that the major element composed the formed sediment was chromium presented as Cr(OH)3 precipitate. The features characterizing Cr(VI) reduction by Achromobacter sp. Ch1 are high Cr(VI) concentrations and high pH.

Jan 1, 2006

By G. Cifuentes

It's know that the cathodic purity and the electrolyte treatment is affect for the solid present in the electrolyte. Anodic slimes properties (f.e.: chemical composition, crystalline composition, sedimentation) was studied in copper electrorefining, this properties were modify through by anodic composition and current density. In this paper will be present only the preliminary anodic slimes relationship at different lead anodic composition. The anodic material was doped during the poured process with lead at different composition. It's confirm the apparition of the (Bindheimitte) SMbz07. The specific gravity of this specie is approximately 7.3 - 7.5, with this values is biggest the probability of sedimentation and smaller the slimes not sedimentabel.

Jan 1, 1999

By Eliezer Martinez-Jimenez, Gretchen T. Lapidus

"Electro-assisted reduction is an effective pretreatment to render chalcopyrite less refractory towards oxidative leaching. In this process, chalcopyrite is selectively converted to chalcocite or copper metal in an electrolytic cell under ambient conditions, while ferrous ion is leached into solution. However, the reaction velocity is hampered by the formation of a ferrous sulfide passivating layer on the solid surface, especially at elevated solid to liquid ratios. In the present work, several strategies for overcoming this problem were evaluated. On one hand, specific ligands for ferrous ion were added in order to increase its solubility and, on the other, an anode material which promotes the oxidation of the sulfide ion was chosen. Leaching tests showed citric acid to be an effective ligand for both ferrous and ferric ions and, in combination with a lead-silver anode, significantly increased the kinetics of chalcopyrite reduction and subsequent copper leaching.IntroductionAttempts to oxidize chalcopyrite at a rapid rate in aqueous solutions, below their normal boiling point, have met with difficulties because of passivation by some of its own components. An alternative line of research explores reductive pretreatment, transforming the chalcopyrite into less refractory copper phases, which can later be oxidized. A recompilation of these efforts up until 2000 was published by Dreisinger and Abed [1]. However, this practice usually requires large excesses of reducing agents, such as copper, lead, aluminum or iron, and in this last case at near-boiling temperatures, in highly"

Jan 1, 2012

By In-Hyeok Choi

Currently, spent V2O5–WO3/TiO2 catalysts contribute significant amounts of solid waste following increasing levels of global demand. V2O5–WO3/ TiO2 catalysts usually consist of TiO2 anatase as a supporting oxide, vanadium as a catalytic agent, and other promoters such as tungsten, silicon, and calcium. Although vanadium is the main catalytic agent, a relatively high content of tungsten (WO3, 7–10 wt%) typically exists compared to vanadium (0.5–1.5 wt%). Considering the irreplaceable properties and industrial importance of tungsten, a feasible method for the recycling of spent V2O5–WO3/TiO2 catalyst should be established to utilize it as a secondary source. This paper presents a process to recover tungsten from spent V2O5–WO3/TiO2 catalyst. The processes proposed here involving roasting, decomposition using HCl, ammonia leaching, and crystallization. Within the process, ammonium paratungstate (71 wt% as WO3) is obtained as a final product. The total yield rate of tungsten from feedstock was found to be 96.3%.

By Tejs Vegge

The lack of suitable means of storing hydrogen for use in the transport sector is generally viewed as a primary showstopper for a hydrogen economy. Recent developments within solid state hydrogen storage in complex hydrides and metal ammines have sparked new hope of a long term solution, but as of now, no materials fulfill all the DoE targets for onboard storage [1]. A detailed physical understanding of the ab-/desorption processes and the role of the essential catalytic additives is an essential prerequisite for the development of new optimized hydrogen storage systems. Here, we illustrate the potential of utilizing the synergy of combining state-of-the-art in theoretical methods and experimental techniques in the analysis and design of materials for hydrogen storage. Recent advances in computer hard- and software has made it possible to treat many of the essential problems in such materials, i.e. structural stability, hydrogen dissociation and diffusion, with high accuracy methods like density functional theory. We rely on such results to guide our synthesis of new materials, and to interpret our experimental results from, e.g. time dependant in situ x-ray diffraction, synchrotron/neutron experiments, and advanced materials testing. Through a continuous feed-back optimization loop between theory and experiments, the obtained nano-scale insight is used to expedite the design and development of novel materials for hydrogen storage.

Jan 1, 2006

By Ken-ichi Miyazawa

A Center of Excellence (COE) titled the Creation of Nature-Guided Materials Processing, called Nature COE, has been established at Nagoya University. In the Nature COE, a new field of material research is being developed through learning the laws of nature, namely, methods of attaining ?appearance of the maximum function under the minimum substance and energy consumption?, which the nature and living organisms have acquired through their evolution in long period. As one of the specific features, an ?Open Cluster Program? was originated for promoting the researches conducted by young researchers and Ph.D. students with those in and out of the university and also for fostering them, together with such educational programs for Ph.D. students as the research incentive, the oversea training and the international lodging seminar programs. The Open Cluster Program has been found to be effective for fostering of young researchers and students, for promoting their researches, for gathering researchers and knowledge from the world and for propagating the research fruits. Through conducting these programs, world-highest intelligent fruits and a gathering of young minds to lead the new field are expected. In this COE, the researches are conducted on (1) materials used for living bodies, (2) mimicking structures which nature or living bodies are forming and (3) materials processing by mimicking processes to form the structures observed in the nature or the living bodies. These researches are conducted by four groups to extend the processes observed in the natural world to a new type of processing that is thoroughly rationalized by plunging a scalpel of engineering, and to establish a new academic field of materials science and engineering.

Jan 1, 2006

By Karin Soldenhoff

Recovery of uranium in conventional ion exchange circuits, using strong base or weak base resins containing quaternary or tertiary amine functional groups, is based on an anion exchange mechanism. In saline liquors, chloride competes with uranium for the active resin sites and reduces resin loading. This results in significant negative impacts on the IX process in terms of plant throughput and operating costs. In this paper we present the results of a study on the recovery of uranium from an acidic in situ leach liquor containing approximately 9 g/L chloride. A range of resins was tested, and a high capacity strong base resin was identified with significantly enhanced loading compared to conventional resins. Other process-relevant criteria such as loading kinetics and elution efficacy are also discussed. The process developed was successfully tested during a recent ion exchange pilot plant operated in conjunction with a field-leach trial.

By Alan Branham

The Mike deposit is a large, low grade, oxide, gold-copper system found at the intersection of two major faults that bound the Carlin Window, Eureka County, Nevada. Disseminated gold occurs within metamorphosed and hydrothermally altered silty limestone (Silurian-Devonian Roberts Mountains Formation), beneath 182 m (600 feet) of barren Tertiary sediments and tuffs. A supergene copper oxide blanket occurs beneath and locally overlaps the lower portion of the gold zone. Decalcification argillization, silicification, and brecciation are superimposed on earlier calcsilicate hornfels and marbles. Altered dikes and sills intrude the gold zone and are locally auriferous.

Jan 1, 1995

By Ejike Emmanuel, Nwoye Chukwuka, Ogwuegbu Martin, Asuwaji Ayuk, Onyedika Gerald

"Microwave pre-treatment of cassiterite ore prior to leaching was carried out in an attempt to obtain high grade of Sn02 and to conserve the total energy expended during processing. Microwave treatment was selected due to the presence of associated minerals which behaves differently to microwave energy. Studies in this work showed that microwave pretreatment of cassiterite ore can be applied to increase the recovery of tin oxide within 5 minutes of leaching. Microwave treatment of the ore resulted in mineral liberation at all particle sizes. Tin oxide was separated from the major impurities via leaching in potassium hydroxide solution and precipitation, resulting in 98% Sn02 at pH 7.IntroductionIn the nineties, the available techniques used for ore processing and analysis in Nigeria was the solution methods of either alkaline fusion or acid digestion [1,2]. A process in which cassiterite is made acid soluble by reduction to SnO2 , which stabilizes by glass formation and the tin was extracted by leaching the glass with sulphuric acid, followed by electrowinning was reported [3,4]. In another study, Baba et al [5] studied the dissolution kinetics of a Nigerian casiterite ore in hydrochloric acid solution. The effects of acid concentration,temperature, particle size and stirring speed were examined. It was found that the dissolution rates of cassiterite depends on hydrogen ion concentration, H+, stirring speed and ore particle dimensions. These were believed to report low data due to incomplete solubilization of the ore minerals in aqeous medium [6]. Analytical chemists have used microwave heating devices routinely for the dissolution of metals, minerals and various chemical products in chemical analysis [7,8]. It offers faster heating rate and consequently faster dissolution rate than conventional heating. The principle of the dissolution of analytical samples has been applied to the leaching of various minerals contained in an ore or concentrate sample. Some researchers [9, 10] conducted microwave assisted leaching of laterite ores containing oxides of nickel, cobalt, and iron. The metals of these mineral components were converted into their chlorides by microwave heating (1200 W, 2450 MHz, Nz atmosphere) a mixture of the ore and ammonium chloride between l 77°C and 312° C for 4-5 min, followed by water leaching at 80° C for 30 min. Nickel and cobalt extractions were 70% and 85%, and respectively, and are comparable with roasting at 300°C in a conventional rotary kiln for 2 hours."

Jan 1, 2013

By Pengkai Wang, Huimin Lu, Xiaoxiang Zhang

"In this paper, it was studied an electrochemical reduction process of carbon dioxide in ionic liquids such as 1-n-butyl-3-methylimidazolium hexafluorophosphate ([Bmim] PF6) as the electrolyte. The electrolysis experiments were carried out under current and potential controls. The cathode products contained carbon nanotubes, carbon nanofibers, nanographites, and amorphous carbon. To establish the actual current and potential ranges, the electroreduction of carbon dioxide dissolved in the ionic liquid was studied by cyclic voltammetry on glass-carbon (GC) electrode at room temperature. The electrochemical mechanism of carbon dioxide electroreduction was studied for explanation of all obtained results. Carbon dioxide in ionic liquids was electroreduced, similar to metals oxides being electroreduced in molten salts.IntroductionGlobal warming caused by the increase of carbon dioxide in the atmosphere has become one of the most concerning environment problems, so the solution to this greenhouse effect is very urgent. However, the carbon dioxide is also a cheap and abundant raw material that represents a potential source for the production of chemicals and fuels. Therefore, the development of the technologies that achieve simultaneous reduction and conversion of carbon dioxide to fuels is important. The electrochemical reduction of carbon dioxide is one of the effective approaches to transform CO2. Many investigations have been carried out on the electrochemical reduction of CO2 in both aqueous [1] and non-aqueous [2] electrolyte solutions with different electrodes. The solubility of CO2 in water is very low even under high pressure of CO2, and some investigators have brought focus into the electrochemical reduction of carbon dioxide in organic solvents, because they dissolved much more CO2 than water did. However, the hazardous or toxic properties of organic solvents hinder their use."

Jan 1, 2009

By Tian Sugui

By means of the long-term aging treated, creep properties measuring and microstructure observation, an investigation has been made into the microstructure and creep behavior of the casting and rolling GH4169 superalloy after long-term aged. Results show that, after the casting and rolling GH4169 superalloy treated by long-term aged, significant amount of " phase are dispersedly precipitated within the grains of the alloy, and some of the NbC, Cr7C3 carbide are distributed along the grain boundaries. In the range of the applied stresses and temperatures, the creep activation energies and stress exponents of LTA GH4169 alloy during steady state creep are calculated to be Q=541.1kJ/mol and n=16.2, respectively. During creep, the deformation mechanism of LTA GH4169 is thought to be the twinning and dislocation slipping within the twinning regions, and the damaging mode of the alloy is the intergranular fracture, and the non-smooth crystal surface is displayed in the fracture regions of the alloy. Thereinto, the carbides film formed along the grain boundaies has a few effect on the strength between the boundaries, which is a main reason of resulting in the alloy possessing a longer creep lifetimes.

Jan 1, 2009

By Junji Shibata

Heavier rare earth, which is contained in a small amount in ores such as bastnesite and monazite, has been accumulated as a heavier rare earth residue without doing separation and purification due to the lack of suitable methods. The heavier rare earth residue includes seven rare earth elements such as Tb, Dy, Ho, Y, Er, Tm and Yb. Separation and recovery process of Dy, Y, Tm and Yb from leached solution of the heavier rare earth residue was investigated by using a column method with solvent impregnated resin. The solvent impregnated resin was prepared by impregnation of organophosphorous extractant whose trade name is PC-88A into a macro porous resin, Amberlite XAD-7. It was almost impossible to separate them in simple adosorption and elution steps. However, we attained to individually separate Dy, Y, Tm and Yb from the leached solution first by changing eluent concentration gradually from pH2 to 0.02kmol/m3 HC1 in the elution step, and secondly by using a development column and changing eluerit concentration in the elution step. The separation process flow was proposed for a heavier rare earth residue by using the solvent impregnated resin method.

Jan 1, 1998

By Wei Liu

A new process for extracting cadmium from the electric precipitated dust produced by ISP process was studied. A leaching rate of 89.1% of cadmium was attained by leaching the dust with NH3?H2O-(NH4)2SO4 system under the best leaching conditions: ratio of liquid to solid(l:s)=2.5, c(NH3):c(NH4+)=3:5, total concentration of ammonium and ammonia=8 mol?L-1, leaching time= 1.5h, temperature=35. The most troublesome impurity of lead could be deposited from the leached out solution automatically after put it static more than 15h when the total concentration of zinc and cadmium was up to 45gL-1 , and the final concentration of lead was 0.0047 gL-1, which meant 99% of it was removed. Metallic cadmium which contained cadmium more than 99% was prepared by electrowinning under the conditions: current density=750Am-2, total concentration of Cd2+ and Zn2+>25gL-1. The current efficiency was about 87% and the energy consumption for every ton of cadmium was about 548KWht-1. Main impurities of the metallic cadmium were copper and zinc and all of they could be got rid of in the following pyrometallurgical refining step.

Jan 1, 2006

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 Antonio Huerta

The effects of potassium ethyl xanthate collector and potassium dichromate used as a depressor on a PbS mineral were studied by high frequency impedance technique. Measurements of complex permittivity, at 100 MHz suggested that is possible to obtain from isotherm adsorption the adequate industrial collector concentration being this in the range of lE-3 to 5E-3M of KEX. The e' values (320-420) in the PbS-KEX system was increased as the KEX concentration was lowered). In the other hand the PbS- K2Cr2O7 system showed higher values of e' (420-510) as the K2Cr2O7 concentration was increased. The PbS-KEX-K2Cr2O7 system was evaluated.

Jan 1, 1997

By Daojin Cao

The chemical components in the saturated aqueous solution of ammonium dimolybdate (ADM) were investigated at room temperature by comparative Raman spectroscopy. In order to explore the further detailed results, a new method of qualitative and half quantitative analyses, based on the main vibrant frequencies and the intensity ratio of the strongest peak to the second strongest peak recorded in Raman spectrum of saturated aqueous solution of ammonium heptamolybdate tetra hydrate (AHM), was put forward and attempted to analyze the chemical components of saturated aqueous solution of ADM. The results showed that there was obvious difference between Raman spectrum of saturated aqueous solution of ADM and that of ADM, but there were good relationships between Raman spectrum of saturated aqueous solution of ADM and Raman spectra of the three samples including AHM, the saturated aqueous solution of AHM and monomolybdate ion in aqueous solution. It was found that aggregated dimolybdate ion ({Mo2O72-}n)did not exist in the saturated aqueous solution, and was changed into heptamolybdate ion (Mo7O246-) and monomolybdate ion (MoO42-), which were in equilibrium each other, but the distribution ratio of heptamolybdate ion was larger than that of monomolybdate ion. In addition, Raman spectral pattern of saturated aqueous solution of ADM was reported.

Jan 1, 2006

By Animesh Jha, Catherine Davey

"Carbothermic reduction and nitridation reactions using synthetic kaolinite mineral were investigated for the formation of silicon based nitrogen ceramics. The temperature dependence of the reaction rate and its effect on phases formed are reported. The effect of the reactivity of carbon on the kinetics of formation of AIN and ShN4 is discussed. Using the standard Gibbs free energy values for the formation of nitrides and oxides of aluminium and silicon, a log po2 verses I/T diagram is constructed. The experimental data results are discussed and compared with the predicted phase equilibria. We also report the influence of sub-oxide gaseous species on the microstructure of the ceramic phases produced.IntroductionSynthetic kaolinite is a clay containing alumina, silica and water of crystallisation, and has a chemical formula 3(Al2O 3.2SiO2.2H2O). This mineral is relatively inexpensive and, is therefore an ideal candidate for use in the production of ceramic powder mixtures for example silicon nitride and aluminium nitride for composite material formation, When the mineral is heated, the water of crystallisation from the crystal lattice is lost via the 3(Al2O 3.2SiO2.2H2O) = 3(Al2O3.2SiO2) + 6H2O reaction. It has been shown [1·2j that on further heating to 1673K, the anhydrous kaolinite decomposes to a mixture of mulllte and silica, 3(Al2O3.2SiO2) = 3Al2O 3.2SiO2 + 4SiO2 which is consistent with the alumina-silica phase diagram, shown in figure 1.The binary alumina-silica phase diagram has a well-defined sub-eutectic immiscibility dome and this characteristic dernixing behaviour is reflected in the thermal decomposition of anhydrous kaolinite consequently the microstructural features resemble the spinodal decomposition process. It is well established that the spinodal decomposition process raises the nucleation frequency due to their low free energy barrier, (?G). The small magnitude of this barrier consequently promotes the evolution of a very fine microstructure. The process of spinodal decomposition is therefore expected to be influential during the reduction-nitridation of kaolinite minerals."

Jan 1, 1996

By Ju Shao-hua

Although nowadays gold extraction methods are very abundant, none of them is satisfying, especially, in the field of heap leaching of low grade gold ore. The traditional heap leaching method of cyanide method plays an inglorious role of badly environmental pollution. In this paper, a bran-new and innoxious method of gold extraction system, metal-ammonium-chloride-ammonia (MACA), was proposed, and also analyzed both thermodynamically and practically. Thermodynamically, according to the principles of simultaneous chemical equilibrium and electronic charge neutrality, the thermodynamics of Au-NH4Cl-NH3-H2O system was studied by using the exponential computation method and through MATLAB programming, and the solid figure of its potential - c(NH4Cl) - c(NH4OH) was drawn. The results showed when the concentrate of ammonia is higher than 0.6 mol?L-1, fAu+/Au is only about -0.2 v. Practically, the leaching results of a cuprous gold ore showed that the extraction of gold can reach to 80% in this system. The preliminary results of reduction of the rich solution with copper and zinc powders showed that with deoxygenizing, the reduction effects were relatively good. These new findings and results have established a theoretical and practical base for developing a new process for heap leaching of low grade gold ores in this system. And the new process owns a series of merits such as, non-cyanogens, nontoxic, broader applicability.

Jan 1, 2006

By K. Twite, K. Mujinga, J-M. Dereydt, P. Louis

"GECAMINES is a large mining concern and the world's leading cobalt producer having some of the richest cobalt deposits in the world. Cobalt is associated in the ore with copper as sulphides and oxides and in some locations with nickel too. Specific hydrometallurgical processes have been developed by GECAMINES which had done an important contribution to the development of the cobalt hydrometallurgy.In the Shituru plant, cobalt is obtained from an unique in-pulp electrolysis process, while in Lullu, cobalt is electrolyzed in a clear acidic solution giving a purer deposit. In the beginning of 1996 Shituru started the treatment of mixed Cu-Co-Ni Shinkolobwe hydrates obtained as by-product of an uranium solvent extraction plant. A typical analysis of this feedstock is: 2% Cu, 8% Co and 4% Ni.The nickel sulfide depolarized cementation process developed previously by GECAMINES was inefficient to treat such a high level of nickel contamination and it was decided to produce alloyed Cobalt-Nickel cathodes in the Shituru tankhouse.As anticipated from laboratory tests as previous studies and publications, a lower Ni/Co in the deposit was obtained compared to the Ni/Co ratio solution, despite the nickel reversible electrochemical potential is somewhat higher than the one of cobalt (-0.25 V vs -0.28 V).In this paper, the process flow-sheet and production data are given. Cobalt alloy with 5 - 20 % Ni was obtained at a production level of 300 t per month. The process developed is a new contribution to cobalt hydrometallurgy."

Jan 1, 1997