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By C. Y. Jia

Adsorption of Thiooxidans ferrooxidans and Mycobacterium Phlei on the surface of pyrite and galena was studied. From the experimental results, it was observed that Mycobacterium Phlei adsorbed preferentially on pyrite than on galena at neutral and alkaline pH values, while Thiooxidans ferrooxidans is not at all pH range, and the scanning electron microscopy photograph also indicated that. FTIR and XPS of two strains of bacteria indicated that there are much functional groups on surface of them, such as O?H, N?H, C-O, C?N, C?O etc, but S-O group occurred on Thioox-idans ferrooxidans cell surface and the P-O group appeared on Mycobacterium Phlei cell surface, and the content of C?O?H and C?O?C groups on Mycobacterium Phlei cell surface is higher than that on Thiooxidans ferrooxidans cell surface, this also been known from UVS investigation. The affinity of these groups to metal ions on sulfide minerals is able to explain the selective adsorption.

Jan 1, 2014

By Vinay Jain, Dharmendr Kumar, Beena Rai, Venugopal Tammishetti

"Selective dispersion-flocculation is considered to be an effective process for the beneficiation of ultrafine particles. This process is based on the preferential adsorption of a flocculant on the mineral particles to be flocculated, leaving rest of the mineral suspended. It has been successfully implemented at plant scales for the beneficiation of ultrafine particles of iron ores, for which conventional methods such as gravity separation, magnetic separation and flotation do not work efficiently. However, the key element responsible for the success of any selective flocculation process is the appropriate choice of the flocculant used for achieving the desired selectivity. At our lab, we are working on design and development of such selective reagents for mineral processing applications, including the beneficiation of iron ore slimes, using a combined molecular modeling and experimental approach. In this study we have employed density functional theory (DFT) to calculate the interaction energies and explain the interaction mechanisms of chitosan with the main minerals present in iron ore slimes, namely, hematite [a-Fe2O3], goethite [a-FeO(OH)], gibbsite [a-Al(OH)3] and kaolinite [Al2Si2O5(OH)4]. The magnitudes of the computed interaction energies follow the trend: Hematite > Goethite > Gibbsite ~ Kaolinite Al-OH terminated > Kaolinite Si-O terminated Analysis of the optimized geometries and electronic structures reveals that the O & N atoms of chitosan molecule form coordinate bonds with surface Fe-atoms of hematite while only weak hydrogen bonds are formed in the case of goethite, gibbsite and kaolinite surfaces thus explaining reasons behind the stronger interactions with the hematite surface. The theoretical findings were validated by performing selective flocculation experiments using chitosan as a flocculant. The selective flocculation experimental results show that a final concentrate of ~60% Fe can be obtained from a feed containing 53.13% Fe with Fe recovery of 74%. The mineral estimation in the obtained concentrate indicated that hematite and goethite are recovered in concentrate while gibbsite and kaolinite are rejected in the tails. These observations were consistent with our theoretical findings. Our work highlights the promising role molecular modeling techniques such as DFT can play in the design and development of selective reagents for beneficiation of alumina-rich iron ore slimes."

Jan 1, 2018

By J. C. Wilmot

The chemistry of aqueous cyanide containing species in the presence of reduced sulfur sources was investigated. Reactions were studied as a function of time and tracked using novel analytical techniques developed for the analysis of the species of interest in the sample matrix. Species of interest in this work were ?free? cyanide, thiocyanate, cyanate, metallo-complexed cyanide, and various sulfur and sulfur-oxygen species. The studies were conducted under constant temperature conditions at pH values above 10.5 and in the absence of light in order to eliminate photochemically induced cyanide reaction effects. The reaction products of cyanide when in contact with pure sulfur, pyrite, pyrrhotite, sphalerite, and cinnabar are reported. These data combined with data for cop-per, arsenic and lead sulfides, which have been previously published, are used to predict the fate of cyanides in refractory gold ores containing sulfides. A mass balance on the cyanide reaction products was completed for all experiments. From these studies insight into the chemical relationships of cyanide, the specific metal sulfide, thiocyanate and cyanate have been gained. When looking at the results of the experiments, it was immediately apparent that even though the overall conversions of cyanide to thiocyanate were different, most of the samples exhibited a similar pattern of reactions. The recovery of cyanide in these experiments was better than we expected, averaging in most experiments to be over 90 percent. Based on this research, the formation of cyanate was probably the main route of loss. The pathway choice for the various minerals was also elucidated in these experiments. The competitive oxidation pathways that cyanide can take have been tracked for sufficient time to determine the ?final? fate of cyanide in a process. Initially, it was thought that the cyanate may be involved in a hydrolysis reaction to form ammo-nia and carbonate ion, but upon further inspection of the data, there was not the drop-off in total cyanide recovery that would manifest itself were this to happen. On the other hand, the hydrolysis of thiocyanate to cyanate and sulfate would require oxidizing conditions which did not exist in solution at the beginning of the experiment. If the solutions were to be sufficiently oxidizing in nature for this to happen, the initial amount of cyanide would have been converted to cyanate quickly. The data support premise that the ?hydrolysis? of thiocyanate to cyanate and sulfate occurs to some extent in the experiments conducted. Knowledge gained from the experiments with pure metal sulfides helped interpret the results of experiments with refractory ores found in the State of Nevada.

Jan 1, 2014

By V. Ross

"The Upper Group 2 (UG2) reef in the Bushveld Complex in South Africa hosts an estimated 40% of the world’s Platinum Group Metal (PGM) resources. The processing of this ore via flotation poses two particular challenges: limiting the levels of chromite in the concentrate to reduce downstream smelting problems, and enhancing the recovery of ultrafine (typically -10 micron), liberated PGMs. Conventional ways of suppressing the entrained chromite, such as froth washing, is not effective in PGM operations, which are dominated by mechanical cells. The recovery of fine particles is hampered by low collision efficiencies with air bubbles, as well as oxidised surface layers especially in tailings operations. This paper documents the results of laboratory tests on a run-of-mine PGM UG2 ore, investigating the application of a pneumo-mechanical column (PMC) and its effect on PGM flotation and its selectivity with regard to chromite. A key feature of the device is the stage-wise release of aerated slurry from an agitated downcomer, thus creating conditions where the superficial velocity profiles of air and slurry change axially within the separation zone. This aids segregation of the silicates and chromite-rich fractions in the separation zone, concentrating the latter towards the bottom of the column and minimising its entrainment into the concentrate. Comparison of the performance of the PMC to that of mechanical laboratory cells under equivalent operating conditions showed improved PGM flotation kinetics and recovery. This was accompanied by a decrease in gangue recovery compared to the mechanical cells by more than 40%, thus doubling the final rougher concentrate grade from 50 to 100 g/t. Significantly, whilst the overall Cr2O3 recovery was reduced by more than 60%, the selectivity (PGM recovery vs Cr2O3 grade in the concentrate) was doubled.INTRODUCTIONThe Bushveld complex in the northern part of South Africa hosts the world’s largest reserves of Platinum Group Metals (PGMs), representing approximately 40% of the total PGE. It is characterised by three main PGM bearing reefs, namely Merensky, Upper Group 2 (UG2) and the Platreef. The Merensky and Platreef are dominated by silicates in the form of pyroxenites, and carry economically recoverable amounts of copper and nickel, in the form of chalcopyrite and pentlandite. The UG2 on the other hand is a chromitite ore with chromite as (ideally, FeO.Cr2O3) the most abundant gangue, often constituting more than 70% by mass with a PGM grade of around 4.5 g/t. Other key gangue minerals are pyroxene, feldspar and talc. The PGEs occur in a wide variety of minerals, with platinum and palladium sulphides typically accounting for about half of the total. Base metal sulphides such as chalcopyrite, pentlandite and pyrrhotite occur in only very minor amounts, accounting mostly for less than 0.1% by mass."

Jan 1, 2018

By Elves Matiolo

This paper describes, in detail, results obtained from a research study of a complex iron ore aiming to produce a pellet feed concentrate with at least 65% of Fe and less than 3.5% of SiO2 in the final concentrate. The work includes an ore desliming followed by column flotation at laboratory scale. The ore sample was from Carajás province - Brazil and represents a complex low grade compact itabirite ore, analyzing 35.9% Fe, 45.1% SiO2 and 0.57% of Al2O3. Yet, the feed was treated previously by magnetic separation and grounded to 97% < 20 µm; this sample was named MAG 2. The chemical and mineralogical characterization of the MAG 2 sample showed that Fe and SiO2 grades were 50.7% and 24.3% respectively and was composed mainly by hematite, goethite and quartz. The particle size distribution, using a laser diffraction technique, showed that 90% of the particles were < 18 µm; 50% less than 8 µm and 10% minor than 1 µm. When the cationic reverse flotation without desliming was tested the selectivity of the process was very low and did not meet the concentrate metallurgical goals of the pellet feed product. However, when desliming was applied prior to flotation, a concentrate product with chemical characteristics of the pellet feed was obtained. The best results after desliming and column flotation achieved global iron metallurgical recovery of 72% with Fe grade in the concentrate of 66.5% and 2.1% SiO2 using starch as depressant for the iron oxides minerals at 1200 g/t ? 1500 g/t and an amine as the quartz collector at 100 g/t concentration (pH constant, at 10.5). It is believed that the desliming stage was key in the separation of the iron bearing particles and has a high potential for the flotation process of this type of ores.

Sep 1, 2012

By S. Z. Khan, Veerendra Singh, Y. Rama Murthy, S. Prasad, Sunil Kumar Tripathy, Gajanan Kapure

"In this study, a low-grade ferruginous low-grade chromite ore was subjected to reduction roasting by using conventional heating as well as microwave heating. Sukinda chromite ore deposit contains majorly iron-bearing minerals as gangue phase. The magnetic susceptibility of these minerals enhances effectively after reduction roasting. Alteration of crystalline structure and magnetic property of these metals enables separation of low-grade ore by using magnetic separation. Conventional roasting studies by varying the temperature, time of reduction and reductant dosage were changed for low-grade ferruginous chromite ore. Similarly, microwave power, retention/exposure time and reductant dosage varied for reduction roasting studies under microwave environment. It is found that low-grade ferruginous chromite ore can be upgraded by reduction roasting and 61.2% Cr2O3 was recovered with a chromium-to-iron ratio of 1.93 from feed chromium-to-iron ratio of 1. Microwave reduction roasting studies resulted in upgradation of chromium-to-iron ratio to 1.73 with a recovery of 21% Cr2O3.INTRODUCTION The chromite ore occurs as a spinel containing oxides of chromium, iron, magnesium and aluminium. Most of the Indian chromite deposits are of ferruginous (rich in iron content) which indicates the abundance of ferruginous gangue minerals along with chromite. The primary use of chromite ore is towards the production of ferrochrome alloys. Chromite ores with less than 40% Cr2O3 and the chromium-to-iron ratio (Cr-to-Fe ratio) <1.8 is considered to be unsuitable for the smelting process (Tripathy et al. 2012, Tripathy et al. 2012a). A considerable amount of low-grade chromite ore and overburden excavated during chromite mining is getting accumulated every year, causing a threat to the environment. Its disposal poses a significant challenge and, hence, the beneficiation of low-grade chromite ore and its utilisation has been attracting a lot of attention. Different physical method of beneficiation methods is generally employed for the improvement of the Cr-to-Fe ratio (Tripathy et al. 2012, Murthy et al. 2011, Tripathy et al. 2012a, Tripathy et al. 2013, Tripathy et al. 2016, Tripathy et al. 2017, Tripathy et al. 2017a). It is observed that the enrichment of the chromite ore is carried out by using gravity and in some places by magnetic separation. However, the enrichment of Cr-to-Fe ratio from low-grade ferruginous chromite ore is difficult by using the above-mentioned beneficiation methods due to the presence of near gravity and near-magnetic susceptibility minerals along with chromite. However, an alternative beneficiation method is needed to explore for the beneficiation of such mineral deposits. Reduction roasting followed by magnetic separation is an alternative option for the separation of these types of ores which is widely reported for the iron and manganese ore (Li, et al., 2010; Chun, et al., 2014, Rath et al., 2018). These processes are majorly focussed on differentiating the magnetic susceptibility between minerals and subsequent separation by using magnetic field. The main advantage of such method is dry process option along with the pre-processed product for the costly smelting process. Also, the roasting of minerals in a microwave environment is also an active research topic in the recent time. So, the amenability of the separation feature of the roasting process by using conventional heating as well as microwave heating can be can be studied for the low grade ferruginous chromite ores."

Jan 1, 2018

By M. R. Garmsiri

With the environmental issues and water recycling becoming more significant, the development of deep cone thickeners has improved the efficiency of thickening. While deep cones performance is dependent on many factors, the sensitivity of an industrial thickener to each variable factor has not been determined. In this work, four industrial deep cone thickeners, which are used on tailings stream in Shahrebabak Copper Complex, were monitored for a year to analyze the effectiveness of different factors affecting the performance. Feed flow rate, fine fraction of the feed, solids concentration, flocculant dosage and concentration, solids density, pH, temperature and bed height were the factors investigated on the basis of partial R2 and partial correlation. Results indicated that, with positive effect, feed slurry dilution affected the dewatering efficiency most sensitively. With a negative effect, the sensitivity of dewatering efficiency of deep cone thickeners to flocculant dosage was negligible. While, decreasing flocculant solution concentration had a considerable positive effect.

Sep 1, 2012

By H. Kasaini

Batch wise adsorption tests for platinum (Pt) on the surface of activated carbon pellets (Norit RO 0.8 BET surface area 1100 mg/g) were carried out in mixed chloride solution. The purpose of this study was to assess and compare the adsorption performance of amine-treated activated carbons (AACs) and native activated carbons (NACs) in terms of adsorption capacity and selectivity. The effect of pH and temperature on adsorption capacity and selectivity was established. The amine- treated ACs were prepared by anchoring the amino groups (butyl amines) on the surface of AC pellets in aqueous media and the UV-Vis was used to determine the amount of amine sequestered from solution by ACs. The dosage of butyl amine on the surface of ACs averaged 0.15 g/g, carbon. The adsorption mechanism was described by the ionization and complexation model whereby interaction between the protonated AAC surface and the anionic chlorocomplex ions (PtCl5 [H2O]-, PtCl62-) proceeded by either electrostatic attraction or/and by covalent bonding [(NH3)2PtCl6 or (CH2COO)2PtCl6]. By comparison, the adsorption capacities of Pt on amine-treated ACs and native ACs were 53.8 mg/g and 33.03 mg/g, respectively which highlight the benefits of anchoring functional molecules on ACs. The selectivity of AACs was influenced by solution pH. Pt adsorbed selectively on the surface of amine-treated ACs at pH<1.5. The highest separation factor that was recoded pertained to Pt and Fe species (ßPt/Fe = 90) then followed by Pt and Ni species (ßPt/Ni = 30) or Pt and Cu species (ßPt/Cu = 15). The lowest separation factor was recorded for Pt and Cr ions (ßPt/N= 5). Adsorption kinetics of Pt on amine-treated AC surfaces, according to the first and second order reactions, were investigated and results showed that rates were in the order 10= 5). -4 min-1 and 102 g?min/mg, respectively. The pseudo 1st order kinetics predicted the adsorption capacity of 51.81 mg/g which was almost similar to the experimental value (53.8 mg/g) while the second order rate equation predicted Pt adsorption capacity of 40.1 mg/g. Both The Langmuir and Toth isotherm fitted the Pt adsorption at pH < 1.0. The Freundlich isotherm tended to underestimate the adsorption capacity of AACs.

Jan 1, 2014

By de Vaux. D.

Synthetic water with a calcium concentration of 80 ppm and 500 ppm was prepared and the flotation results obtained compared to a simple electrolyte in order to determine the effect water quality has on pentlandite and pyroxene surface alteration and, ultimately, floatability. During the study, the possible effect of interactions between the minerals investigated and Ca2+ ions in the presence of sodium isobutyl xanthate was studied at pH 6 and pH 9 by means of zeta potential determinations, microflotation tests and ToF-SIMS analysis. The results obtained have demonstrated that water quality does play a significant role in flotation recovery at the experimental conditions used.

Jan 1, 2003

By S. S. Lu

In sodium oleate and salicylhydroxamic acid systems, sequence of floatability of three sulfate minerals is: barite>celestite>gypsum, in lauryl amine system is: gypsum>celestite>barite. XPS and infrared spectrum analysis are used to find that it is chemical reaction between sodium oleate and three minerals, physical adsorption on the surface of minerals for lauryl amine, and it is chelating reaction between salicylhydroxamic acid and three minerals possibly. Theoretical calculation on chemical bonds in crystal structures of three minerals is carried out, finding that breaking degree of Mn+?O2- in crystal structures of three sulfate minerals is closed related with floatability.

Jan 1, 2014

By James D. Bittner

Separation Technologies, LLC (ST) has developed a processing system based on triboelectric charging and electrostatic separation that provides the mineral processing industry a means to beneficiate fine materials with an entirely dry technology. The environmentally friendly process can eliminate wet processing and required drying of the final material. The process requires little if any pre-treatment of the material other than grinding and operates at high capacity ? up to 40 tonnes per hour by a compact machine. Energy consumption is low, approximately 1 kWh/tonnes of material processed. Since the only potential emission of the process is dust, permitting is typically relatively easy. In contrast to the other available electrostatic separation processes that are typically limited to particles greater than 75 µm in size, the ST belt separator is ideally suited for separation of very fine (<1 µm) to moderately coarse (500 µm) materials with very high throughputs. The triboelectric particle charging is effective for a wide range of materials and only requires particle ? particle contact. The small gap, high electric field, counter current flow, vigorous particle-particle agitation and self-cleaning action of the belt on the electrodes are the critical features of the ST separator. The high efficiency multi-stage separation through charging / recharging and internal recycle results in far superior separations and is effective on fine materials that cannot be separated at all by the conventional electrostatic techniques. Since 1995, this triboelectric process has been extensively used for the beneficiation of coal fly ash with eighteen separators in place and over 100 machine-years of operation at locations in the North America and Europe. The technology has been also successfully applied to the beneficiation of a variety of minerals including calcium carbonates, talc, and potash.

Sep 1, 2012

In the present work, the flotation behaviours of zircon, rutile and ilmenite using sodium oleate as collector in absence and presence of depressants were thoroughly investigated. The maximum in the flotation recovery of any of the above minerals falls within similar pH ranges. A range of inorganic and polymer depressants were examined in order to improve the separation of zircon from rutile and ilmenite. Optimum values of conditioning pH and depressant concentration to achieve maximum recovery and best selective floatability of zircon were obtained. Selective flotation of zircon from Ti-bearing minerals was anticipated from single mineral experiments under different pH values, depressant and collector conditions.

Jan 1, 2014

By Yuexin Han

The wet preconcentration of haematite, comminuted by high-pressure grinding roller was studied, using the cylindrical ferromagnetic medium. The effects of various factors including rod diameter, rod gap and background magnetic field intensity (BMFI) on the performances of preconcentration for different size fractions and the force analysis of single mineral particles with different diameter in the separation zone were emphatically investigated. The results showed that as the rod diameter increased, the rod gap decreased, and the BMFI increased the tailings grade and the tailings yield reduced while the concentrates recovery raised that was regardless of variations in feed size distribution. For the -3.2+0.18mm size fraction preconcentration, the magnetic medium with a rod diameter of 4 mm and a rod gap of 7 mm at BMFI of 454kA/m is used to get a higher performance. For -0.18mm size fraction preconcentration, the magnetic medium with a rod diameter of 4 mm and a rod gap of 4 mm at BMFI of 263kA/m is used to get a higher performance. After the classifying preconcentration, at the optimum condition, the overall concentrate grade increases by 9.56 percentage points and the concentrate recovery is up to the 82.67% with a tailing grade of 10.68% and a tailing yield of 40.31%. The magnetic force, exerted on weekly magnetic minerals was proportional, to the specific susceptibility and square of BMFI. For the same BMFI, the magnetic capturing force on coarse particles increased, and that on fine particles decreased with the increasing of rod diameter. For the lean locked-particles, considering the gravity and viscous resistance of particles, rods with a big diameter were beneficial to the capture of coarse particles and had no influence on the capture of fine particles, while rods with a small diameter were good for the capture of fine particles and not suitable for the capture of coarse particles of lean locked-particles. Keywords: low grade haematite, high-pressure grinding roller, high intensity magnetic separation, pre-concentration

Sep 1, 2012

By Diogo R. Prado, José Aurélio M. da Luz

Drying operation can have a major importance in a mineral processing undertaking. The proper sizing of dryers can ensure the specified dewatering level without energy wastage. However, often the sizing of fluidized bed is done disregarding the actual residence time distribution (RTD) of the particles inside the reactor. In this case it is usual to adopt the average residence time as a design criterion. In this work, we have quantified the effect of residence time distribution on drying, ensuring that a previously adopted fraction of the particles remains inside the reactor for the required time lapse needed for drying. Design criteria such as particulate flow rate and drying time, taking into account the statistical distribution of residence time was studied, matching the thermodynamic and fluid dynamic aspects of the drying process. Experimental tests carried out have confirmed the RTD for a teetering bed as the same for a canonical ideal mixing system. Although the fluidized bed volume using the proposed formulation was higher than that found for the average time based procedure, the efficiency gain in drying has proven advantageous.

Jan 1, 2014

By Walter W. Focke, Zola Kwela, Willem van der Merwe, Arao Manhique

"The advantages of the de Wet zirconium process for the manufacture of AZST from zircon sand include: Fewer processing steps; removal of radioactivity by leaching rather than by precipitation; alkali reagent recovery in the form of a sodium silicate solution that is essentially free of radioactivity; fewer waste streams and less waste to discard.Here we report on our efforts at maximizing the alkali recovery in the sodium silicate product stream: Milled zircon, d50 ˜ 9 µm, was fused with caustic soda pearls in open reaction vessels at temperatures between 650°C and 850°C. Fusion times of 1, 2, 4, 24 and 336 hours (with intermittent milling) were investigated.For prolonged fusion times the fusion products approached equilibrium compositions. However, the phases Na2ZrSiO5 and Na4Zr2Si3O12 observed at 850°C did not form at 650°C. Since they do not hydrolyse in water they limit the recovery of alkali. For 2-hour fusions a broad spectrum of non-equilibrium reaction-products, that are rich in sodium silicates, is formed. Optimum process conditions, with respect to NaOH recovery, correspond to a 2:1 stoichiometry and fusing for 2-hour at 850°C. At these conditions the alkali recovery is ca. 78% and the zirconia yield is ca. 57%."

Jan 1, 2003

By L. S. Gertsch

The production of minerals for human use at locations other than the Earth is expected to ?advance ? human prosperity in ? ways that [do] not compromise the potential prosperity and quality of life of future generations? (Brundtland, 1987); in other words, sustainably. This paper examines the interaction of extra-terrestrial mineral production (ETMP) with the following sustainability imperatives: ? The sustainability of human activities on Earth; ? The sustainability of human activities elsewhere; ? Human survival in general, the ultimate sustainability goal. Some of the consequences of mineral production on Earth are widely considered to decrease the future prosperity and quality of human life. Examples include noxious by-products or wastes and unsettling economic up- and downswings. Moving mineral production activities to extra-terrestrial locations, where appropriate, will decrease many of its deleterious effects. Terrestrial mineral production presently is decreasing in some countries and increasing in others, moving from the cheaper and easier ores to more expensive, difficult materials. When the full costs of maintaining the terrestrial environment in a sustainable manner are included, total mineral pro-duction costs must increase. The cost of extracting mineral products from extra-terrestrial sources will be substantially higher, especially in the initial phases, but as the full costs of terrestrial production increase, at some point in the future (different points for different minerals), the curves will cross (Fig.1). This will occur at different points for different materials, a process whose prediction will be complicated by substitution of cheaper materials for some uses as prices of the original material rise. In summary, mineral products from extra-terrestrial sources will tend to increase the sustainability of human civilization, once steady state has been reached.

Jan 1, 2014

By Tilak Raj Mankhand, Mudila Dhanunjaya Rao, Kamalesh K. Singh

"Zinc dust is used for the removal of primary impurities by cementation from the zinc sulphate electrolyte before electrowinning of zinc. However, the industrial zinc electrowinning plants has been reported that the zinc dust consumption is in large excess than the stoichiometric requirement. In the present investigation, morphology of the zinc dust has been altered by ball milling and utilized for the cementation of cadmium, which is one of the major impurity and compared the change in the rate of cementation with original zinc dust. Initially, 325 mesh size zinc dust was used for the optimization of the excess quantity of zinc dust to be used at a temperature of 50 °C. The chemical analysis of zinc dust before and after ball milling and morphology were studied by scanning electron microscopy (SEM), and the solution was characterized by Atomic Absorption Spectrophotometer. The rate of cementation increased with increase in ball milling time. The residual precipitate obtained after filtration was also characterized by X-ray diffraction analysis. Finally experiments were conducted to study the effect of temperature and kinetics of cadmium cementation using first order reaction kinetics. Based on the integral method, the calculated activation energy for the cadmium cementation with 4-hours ball milled zinc dust was found to be 3.39 KJ/mole. INTRODUCTION Primary production of zinc in the world is carried out by hydrometallurgical route. The primary impurities in the neutralized zinc sulphate solution that cause negative effect on electrowinning are copper, cadmium, cobalt, and nickel. Copper diminishes the current efficiency and cadmium contaminates the cathode zinc (Morgan, 1977) while electro winning. Nickel and cobalt lead to perforation in the zinc deposit and prevents the electro winning process (Abrasheva et al, 1984). Due to higher electro positivity of these metal impurities than zinc, they can co-deposit with cathode zinc at the time of electrolysis. In addition to that, some possible impurities (including cobalt) in the electrolysis may lower the hydrogen overvoltage, allowing deposition of hydrogen at cathode resulting in fall of current efficiency. The deposition of zinc on the cathode is possible only at higher hydrogen overvoltage which is practicable in the absence of such impurities (Raghavan et al., 1999). Cementation is one of the prominent purification technique, and in that less reactive metal can be replaced by highly reactive metal by allowing them into precipitation. Cementation of cadmium from zinc sulphate electrolyte is being done by the addition of zinc dust."

Jan 1, 2018

Due to complex mineralogical and chemical interactions of the value and gangue mineral phases present in uranium-containing lateritic ores, deleterious pulp gelation which impacts on value metal recovery sometimes occur during atmospheric leaching. In this study, the leaching behavior and particle interactions of selected oxide (hematite, quartz) and clay minerals (muscovite, chlorite), which constitute predominant host gangue phases of typical lateritic uranium ores are investigated to provide basic, mechanistic understanding of temporal pulp gelation phenomenon. Isothermal, batch leaching with H2SO4 was carried out on concentrated dispersions (30 ? 57 wt.%) of single minerals at pH 1 and 25 or 70 °C and their concomitant solution, speciation and rheology (shear yield stress, viscosity) were characterized. It is clearly shown that despite the high oxide content of lateritic ores, the pulp chemistry and rheology is largely affected by the incongruent leaching behavior of more reactive, acid-consuming aluminosilicate clays. Furthermore, time- and temperature-dependent alumino-silicate species polycondensation interfacial reactions are shown to be responsible for the enhanced particle interactions, reflecting strong pulp rheology in agitation and pumping. If not properly mitigated, high pulp shear yield stress and viscosity have a striking impact on processability and hence, value metal recovery.

Sep 1, 2012

Electrochemical behaviors of synthetic and natural enargite in buffer solutions have been investigated using open circuit potential, stationary polarization and cyclic voltammetry as functions of solution pH, scan direction, scan range, scan rate and dissolved O2. The results indicate that the electrochemical behaviors of synthetic and natural enargite are very similar; solution pH, scan direction, scan range and scan rate have remarkable effects on the electrochemical behavior of enargite while dissolved O2 has little effect on the electrochemical behavior of enargite. The potential range in which enargite possesses the ability of passivation is from ?0.9 V to + 0.83 V vs. SCE. Enargite is most stable in neutral and alkaline solution around potential ?0.2 V vs. SCE. The main oxidation products on enargite surface in alkaline solution are Cu(OH)2 while the potential imposed on it is within the range of ?0.2 V to 0.33 V vs. SCE and Cu(OH)2 + S0while the potential applied is higher than 0.52 V vs. SCE.

Jan 1, 2014

By L. Rintala

The design of a hydrometallurgical process starts with the analysis of the raw materials to be treated, for example mineralogy, chemistry, deposit size are analysed. Based on this information suitable unit processes for pre-treatment, leaching, solution purification and product recovery are selected. Typically, process design for the new ore deposit relies on laboratory tests such as pre-treatment and leaching experiments. The experimental work is the most time consuming and expensive part of the process design. Reducing the number of experiments would shorten the time of designing a new flowsheet or development of new process technology. A large amount of information is available about the hydrometallurgical experiments and the amount is increasing continuously. For example, word search using ?hydrometallurgy? from Scopus database results in over 4 000 publications with the word in title, abstract or keywords. This number consists of 2 500 articles, 900 conference papers, and 90 reviews since 1972. The number of hydrometallurgical publications per year has increased from 13 in 1972 to 150-200 in the last few years. The objective of this study was to analyze how detailed data of experiments about the gold extraction is published and how that data could be exploited more effectively when designing hydrometallurgical processing for new ore. The leading idea is that similar ores should have the similar response in leaching. If the published information was used more efficiently, the amount of experiments would be reduced. More than 200 cases of experimental data of gold leaching have been analyzed for this study. There are over 30 factors that could be used in comparison when selecting process alternatives, but challenging fact is that not all these factors are documented in all publications. Results show that the usefulness of the published data in the development of hydrometallurgical flow sheet for gold using decision-support tools is not that straightforward. The quality of the published information about gold extraction varied between the publications and the descriptions of the raw materials, experimental arrangements and results were often missing details. Methods to normalize the data for description of the cases and a system to describe different features unambiguously are needed. Keywords: refractory gold, host mineral, leaching, data analysis, case-based reasoning

Sep 1, 2012