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By Xuliang Yang, Yuemin Zhao, Bo Zhang, Liang Dong, Cheng Sheng, Gongmin Li, Zhenfu Luo, Yaqun He, Chenlong Duan

Coal plays an important role in the primary energy consumption of all over the world. In 2012, coal reached the highest share (29.9%) of global primary energy consumption since 1970. Coal burning mainly contributes to the emission of SO2, NOX, Hg and other impurities that jeopardize the future of environment. . Beneficiation before coal utilization is the most economical and effective technology for removing the hazardous material and gangue. In this paper, a novel process of dry beneficiation based on gas-solid two-phase flow composed of the compound dry cleaning separator (FGX), the air dense medium fluidized bed separator (ADMFB) and the vibrated fluidized bed with autogenous medium (VFB) is proposed. The main equipment and the flowsheet of the united system are described in detail. Separating principle of the FGX, ADMFB and VFB devices are all based on gas-solid two-phase flow. In FGX, gassolid suspension is composed of continuous gas flow and coal powder in feed coal. Large size coal (+6- 80mm) can be pre-separated effectively, and large size gangue can be removed effectively. Moreover, - 6mm particles fed serve as autogenous medium in FGX. The probable E value is 0.13 for -80 mm raw coal. In ADMFB, magnetic powder with -0.3 + 0.045 mm size fraction and coal powder in feed coal are compound medium solids. The separation density can be adjusted and controlled according to properties of raw coal. -50 + 6 mm raw coal can be cleaned efficiently, the probable E value is 0.05. In VFB, -6 + 1 mm coal can be separated. Generally, -80 mm raw coal can be cleaned efficiently in the united system based on gas-solid two-phase flow.

Jan 1, 2014

By L. J. Li, Q. Zhang, Z. H. Liu, Q. L. Chen

Phosphogypsum (PG) is an industrial waste from the production of phosphate fertilizer. The utilization of PG is restricted by its containing impurities, and the pretreatment is crucial to eliminating these impurities. The purpose of the research is to recycle pretreatment PG as raw material for preparation of a-calcium sulfate hemihydrate (a-HH) by salt solution method. The effect of pretreatment technologies of lime neutralization and washing on dehydration rate, phase composition and morphology evolution of a-HH were investigated by crystal water content analysis, XRD and SEM. Furthermore, the change of pH in the reaction process was also discussed in detail. The results show that the dehydration rate of conversion PG to a-HH increases and the corresponding induction period, crystal growth period and total time decrease with an increase in CaO dosage from 0.2% to 0.6%. In the presence of 0.4% CaO or 0.6% CaO, the a-HH presents a long hexagon-prism-shaped crystal with a purity of 94%, and the end face of a-HH presents polyhedron. The system pH sharply decreases with the reaction time under different CaO dosage, and the pH variation from the initial alkalinity to acidity. The main reason is that as the co-crystallized phosphorus dissolved and released HPO42-, and with the pH decreasing to 4-5, HPO42- transformed into H2PO4-. The dehydration rate of washing PG is lower than that of original PG. Compared with the original PG, a-HH with the larger width and smaller aspect ratio can be achieved from the pretreatment PG subjected to lime neutralization and washing, meanwhile the crystal surface is more smooth.

Jan 1, 2018

By Érica Linhares, Anderson Silveira Lopes, Aline Costa

In the production units of ferromanganese alloys wastewater are generated. They mainly arise from gutters of drainage water from warehouse of raw material (manganese ore, reducing agents and other), product and slag. This wastewater, in general, may contain particles that will suffer difficulty to naturally decant, giving the water turbidity and color characteristics. Thus, this study aims to characterize the effluent, the treated water and the sludge from the sedimentation tank from the one main Brazilian plant. The investigated characteristics were: turbidity, total solids (TS), suspended solids (SS), dissolved solids (DS), pH, Eh, COD (chemical oxygen demand), residue classification and chemical analysis by ICP - OES. The turbidity before treatment was 417 NTU and after passing through the tank, 44 NTU, a figure slightly higher than the emission standards for Class 1 regulated by the Brazilian environmental legislation in force. The values for TS, SS and DS of the effluent were 225, 114.3 and 110 mg/L, respectively. For the treated water the values were 93, 48.3 and 45 mg/L for TS, SS and DS, respectively. The sedimentation process was able to reduce by 21 % of the COD. In the test of loss on ignition (LOI) from the tank bottom sludge were observed losses of 29.35 %, while the volatile analysis found 20.70 % of volatiles in the sample. It was determined that the concentrations of Al, Fe, Mn and S are, respectively, 0.1875 mg.L-1, 0.3071 mg.L-1, 0,789 mg l-1 and 0.00828 mg.L-1, values above the maximum allowed by law. Based on the analysis of X-ray diffraction, the identified minerals in the sludge were quartz, muscovite, kaolinite, calcite and albite.

Jan 1, 2014

By Z. B. Pan

The innovative point of this new technology can be described that under normal pressure and 70°C, using a new combined activating and oxidizing agent, the minerals bearing arsenic and organic carbon are oxidized effectively. This technology can be applied in commercial scale. The high carbon and arsenic bearing gold ore is taken from Gansu, where hundreds of tons gold deposit. The ore has 0.51% of arsenic and 1.75% of carbon (1.07% of organic carbon). The gold occurs mainly in native with particle size 0.02~0.6 mm and a few are enwrapped by pyrite and arsenopyrite. The traditional cyanide leaching process gains a very low gold leaching rate with only 5%. Through systemic experimental study, the technological flowsheet of flotation process for concentrating gold, then pre-treating the gold concentrate followed by cyanide leaching the gold concentrate are used. With 4.92 g/t gold of head sample, the gold concentrate with 46.52g/t gold grade and 96.53% gold recovery is gained by flotation process. Followed by pre-treatment for 6 hours, the gold concentrate is leached with cyanide after filtration and washing. The total gold leaching rate is up to 95.44%.

Jan 1, 2014

By M. I. Panayotova

Some of effluents released by copper smelting plants are highly acidic (pH = 0~1) and contain arsenic and copper in relatively high concentrations (10~20 g/L). Usually arsenic is removed by precipitation with different reagents, such as lime, iron salts, calcium salts, aluminium salts, etc. Precipitates (often voluminous) that require further handling are formed and copper and other valuable components are lost. A method is presented for copper and arsenic extraction from acidic effluents. Effluents are treated in specially designed closed electrochemical cell without chemicals? addition. Gases formed are collected and treated for decomposing the eventual traces of As-bearing compounds and ensuring the environment protection. Initially copper of grade of 85 % is electro-won. Further about half of the initially available arsenic is separated as low-soluble, low volume mixture of intermetallic compounds, oxides and some elemental arsenic. At the next stage the main part of the left arsenic is immobilized as low soluble stable compound. Arsenic content in the treated acid is in the range 0.20~0.25 g/L. Acidity of treated effluent after first two stages remains practically unchanged and the solution can be re-used. Physicochemical and electrochemical processes, governing copper and arsenic removal, are discussed.

Jan 1, 2014

By Lev O. Filippov, Inna V. Filippova

"Flotation of metal-organic precipitate in column is sensible to the hydrodynamic conditions determined by the diameter and the dispersion of rising bubbles. Thus, the dissipation energy in the system resulting of ratio between superficial fluid velocities (gas and feed) in the column is the main parameter for precipitate flotation in pilot or industrial scales. The suggested limiting factor is the aggregate stability under the turbulence created by the rising bubbles. The stability of precipitate is related to the structural organisation of aggregates, which determines the size distribution of particles during precipitation and flotation stages.Structural evolution of Mo precipitate and the destruction phenomenon were described by using of the various fractal dimensions. The fractal studies allow the detection of a structural scaled organisation of the precipitate flocs. The fractal dimension of the particle mass distribution Dm=1.94+/-0.15 suggests, for the floc structure, a cluster-cluster aggregation process either with restructuring or breakage phases.The destruction process, which occurs for the lowest values of the dissipation energy E (0.02 . 0.05 W/kg) was characterised by a fractal dimension Dg of size distribution. Besides, the destruction of floc produces very fine particles, and thus induces the difficulties of bubble-particle collision during the precipitate flotation in column."

Jan 1, 2003

By Vasily V. Lodeischikov, Adolf F. Panchenko, Olga D. Khmelnitskaya, Vladimir E. Dementyev

Pilot plant tests of underground gold leaching from Maminskoye deposit oxide ores at a grade of 0,7 g/t Au were carried out. The underground leaching flow sheet includes Au dissolution by chlorine-containing solutions, Au adsorption from solution on active carbon, carbon concentrate ashing and calcine melting to produce high grade gold concentrate. The underground leaching system throughput was 15 m3 of solution per hour. Gold concentration in pregnant solutions was 0.12-0.13 mg/l. Gold recovery from solutions into carbon was in the range of 63-84%. It was demonstrated that the low Au recovery in the adsorption cycle was due to the presence in pregnant solutions of "active" chlorine, which destroys active carbon and causes a sharp decrease of the carbon loading capacity for gold. To improve the adsorption indices, previously dechlorinated pregnant solutions using bituminous coal or Na2S2O3, is recommended. Ion exchange process was tested as an alternative for gold extraction from dechlorinated solutions. In the testwork period, 4.4 kg of gold were produced with a chlorine consumption of 3.5 kg per 1 g of gold. During the tests a program of environmental protection measures was completed to provide the necessary safety precautions of the underground leaching works.

Jan 1, 2003

By Ljubisa Obradovic, Baisui Han, Batnasan Altansukh, Zoran Stevanovic, Atsushi Shibayama, Jonovic Radojka, Daizo Ishiyama, Kazutoshi Hag, Radmila Markovic, Ljiljana Avramovic

This paper discussed a combined froth flotation and high pressure leaching (HPL) process to recover copper from mine tailings. At first, froth flotation were carried out using the mine tailings sample under various conditions in the presence of different pH (3.5-10) and sulfurizing reagent value (0-1000 g/t), respectively. As a result, optimum condition (sulfurizing reagent of 1000 g/t, pH of 10, PAX (collector) of 100 g/t and MIBC (frother) of 200 g/t) was found for froth flotation of copper. The effects of sulphuric acid concentration, leaching temperature, total pressure (steam pressure plus oxygen pressure) on high pressure leaching (HPL) of mine tailing were investigated using sulphuric acid solution in the presence of oxygen. The best conditions for HPL were obtained to be sulphuric acid concentration: 0 mol/L (water), leaching temperature: 170 ?, total pressure: 2 MPa, leaching time: 1 hr and pulp density: 100 g/L. The leaching rate of copper reached nearly 99 % and the concentration of copper in pregnant leach solution (PLS) was 0.24 g/L. Finally, copper in the mine tailing was recovered using froth flotation followed by HPL. As a result of a combined froth flotation and HPL, the vast majority of copper (99 %) from the mine tailings was extracted.

Jan 1, 2014

By Zhou Yucai, Zhou Jing, Zhu Yimim

"In this article, research on the beneficiation process for a carbon containing copper-molybdenum deposit in Henan province has been carried out. The elemental composition, mineral composition and relative content, characteristics of embedded and symbiotic relationship, the forms of the copper-molybdenum particlesand their disseminated features, and particle size distribution have been worked out. Flotation behavior of copper-molybdenum mixed flotation and separate flotation in the systems of different collectors and depressants, and the influence of different flowsheets on the copper-molybdenum separation have been investigated by actual ore flotation tests, The separation problem of copper-molybdenum for a carbon-containing copper molybdenum ore has been solved.INTRODUCTION In this paper, technological mineralogy, small experiment of flotation recovery of copper Molybdenum ore, and expansion experiment of mineral recovery of copper Molybdenum ore are introduced. (1) The results of process mineralogyshow that the content of copper is 0.42%, molybdenum is 0.021% in the raw ore, they mainly exist in the form of sulfide, with low oxidation rate. (2) The results of flotation tests show that the combination of butyl xanthate and isopropyl ethylthionocarbamate reagents is effective collector of copper-molybdenum mixed flotation for carbon copper molybdenum, (3) When the grinding fineness is -0.074 mm taking 71%, and regrinding fineness is -0.038 mm taking 85%, the flowsheet of first copper-molybdenum mixed flotation and then regrinding rough concentrate and last separation flotation of copper and molybdenum was adopted, which realized the effective separation of copper and molybdenum for carbon-containing copper molybdenum ore. Good flotation indexes were gained with copper concentrate containing 20.96% copper and copper recovery 90.06%, and molybdenum concentrate containing 46.78% molybdenum with molybdenum recovery 72.68%. (4) The seven days average concentration index of scale-up the continuous dressing experiment is as follows, the copper content in copper concentrate is 20.16% and the recovery is 89.61%; the molybdenum content in molybdenum concentrate is 24.58% and the recovery rate is 74.09%."

Jan 1, 2018

By Felix M. Zhuravlev, Vitalij P. Lyalyuk

"While there is a large industry based on recovering platinum group metals (PGM) from complex sulphide ores containing Cu and Ni, there is little information on the thermodynamics of the matte phase formed on smelting the ore and in particular the behaviour of Pt in the matte.The equilibrium between metallic platinum and industrial mattes was studied in a series of experiments where a small quantity of matte (5g) and platinum foil of 150 µm thickness (0.5 g) were equilibrated in magnesia crucibles at 1400°C under conditions where the oxygen and sulphur partial pressures were controlled.The chemistries of the phases were determined from EDS analysis using a scanning electron microscope. Line scans were initially used to confirm that the foils had attained a uniform composition across their thickness. The composition of the matte was determined from analysis of an area of matte including the small metallic droplets and dendrites.The distribution of Pt in Cu-Fe-Ni mattes (Pt: 1.5 – 3%) and solid Pt alloys (Pt: 54 – 72%) was studied. For a matte of base composition 45%Fe, 11%Ni, 8% Cu, at a base temperature 1400°C, the following behaviour was observed for the Pt distribution ratio:Under the range of sulphur and oxygen pressure of this study (log pO2 from -15 to –12.2, log pS2 from – 4.6 to –2.2), the distribution ratio of Pt between matte and alloy was independent of the sulphur and oxygen pressure, having a value of 0.04.The Pt distribution ratio increased from 0.02 to 0.08 with temperature from 1340 to 1450 oC.For mattes where the proportions of Cu and Ni were kept constant, a slight decreasing trend was shown for the distribution ratio of Pt versus the iron content (37 to 53%) in the matte but was not confirmed because of experimental uncertainty."

Jan 1, 2003

By Georgios N. Anastassakis

"The depletion of the high-grade chromite ores and the inefficiency of the gravimetric methods to process fine particles has shifted the industrial and research interest from gravimetric separation methods to flotation. However, the response of the minerals to various flotation schemes is not clearly established. In this work, the physicochemical behavior of chromite and olivine is studied using a fatty acid collector.The minerals used were from Vourino area (Kozani, Northern Greece). Macroscopically pure samples of chromite and olivine were selected by hand picking, crushed and subsequently ground to the required size. Each sample was then submitted to panning and magnetic separation for the removal of impurities. The mineralogical and chemical analysis of the purified samples revealed the following: a) The purity of chromite was 95% while the minor constituent was mainly magnetite. Its chemical analysis was: 12.50% Fetot, 2.50% SiO2, 54,54% Cr2O3, 9.31% Al2O3, 0.47% CaO, 13.10% MgO. These analyses show that Cr3+ has been substituted by Fe3+ and Al3+ as well as Fe2+ has been significantly substituted by Mg2+. b) Forsterite is the main constituent of olivine either as pure forsterite (Mg2SiO4), which is the prevailing form, or as iron-forsterite [(Mg,Fe)2SiO4] in less amount. Chrysotile, which belongs to the serpentine group, was also detected at a percentage of 10-15%. The chemical analysis of olivine was: 36.90% SiO2, 0,53% Cr2O3, 7,43% Fe2O3, 0.72% Al2O3, 0.91% CaO, 47.00% MgO, 6.02% LOI.The electrokinetic behavior of the minerals was studied in a electrophoretic mass transport equipment Model 1202 of Micromeritics. The reagents used were sodium hexa-metaphosphate of commercial grade and sodium oleate."

Jan 1, 2003

By Ana C. C. Pacheco, Maurício L. Torem

"The aim of this work was the study of the effect of the type (Fe3+, Al3+ and Fe3+ and Al3+ mixture) and of the coprecipitant concentration on As5+ removal by ACF. Removal of As5+ using sodium dodecyl sulfate (SDS) as a collector was studied by Adsorbing Colloid Flotation (ACF) at laboratory scale. The morphology of the precipitate retained in the foam was analyzed by Scanning Electron Microscopy (SEM/EDS).In order to investigate the effect of the initial concentration of Fe3+ on As removal, sets of experiments were performed with a concentration of Fe3+ in the proper range of pH (5,0 – 6,0) previously observed in the coprecipitation tests. As removal improves significantly as the concentration of the coprecipitant agent increases from 60 mg.L-1 (77,4%) to 80 mg.L-1 (99,7%). This is probably due to the higher concentration of ferric hydroxide (Fe(OH)3) which provides a larger surface area available for adsorption of As. From the initial coprecipitant concentration of 80 mg.L-1, As removal has shown to be rather high (? 99,7%), with the maximum being (99,9%) by using a Fe3+ concentration of 160 mg.L-1. Therefore, for a maximum As removal, under these test conditions, the optimum concentration of Fe3+ is 160mg.L-1.This paper also shows the effect of the initial concentration of Al3+ on As removal at a suitable range of pH (7,0 – 8,0). A very significant increase on As removal was found to occur as the initial concentration of coprecipitant was increased from 60 mg.L-1 (35,7%) to 80 mg.L-1 (97,7%) and a decrease in As floatability (43,7% - 54,5%) was found to occur from that Al3+ concentration amount. Based upon those results, the optimum Al3+ concentration so as to remove As under these test conditions is 80 mg.L-1."

Jan 1, 2003

By Steven Wright, Sharif Jahanshahi, Shouyi Sun

"While there is a large industry based on recovering platinum group metals (PGM) from complex sulphide ores containing Cu and Ni, there is little information on the thermodynamics of the matte phase formed on smelting the ore and in particular the behaviour of Pt in the matte.The equilibrium between metallic platinum and industrial mattes was studied in a series of experiments where a small quantity of matte (5g) and platinum foil of 150 µm thickness (0.5 g) were equilibrated in magnesia crucibles at 1400°C under conditions where the oxygen and sulphur partial pressures were controlled.The chemistries of the phases were determined from EDS analysis using a scanning electron microscope. Line scans were initially used to confirm that the foils had attained a uniform composition across their thickness. The composition of the matte was determined from analysis of an area of matte including the small metallic droplets and dendrites.The distribution of Pt in Cu-Fe-Ni mattes (Pt: 1.5 – 3%) and solid Pt alloys (Pt: 54 – 72%) was studied. For a matte of base composition 45%Fe, 11%Ni, 8% Cu, at a base temperature 1400°C, the following behaviour was observed for the Pt distribution ratio:Under the range of sulphur and oxygen pressure of this study (log pO2 from -15 to –12.2, log pS2 from – 4.6 to –2.2), the distribution ratio of Pt between matte and alloy was independent of the sulphur and oxygen pressure, having a value of 0.04.The Pt distribution ratio increased from 0.02 to 0.08 with temperature from 1340 to 1450 oC.For mattes where the proportions of Cu and Ni were kept constant, a slight decreasing trend was shown for the distribution ratio of Pt versus the iron content (37 to 53%) in the matte but was not confirmed because of experimental uncertainty."

Jan 1, 2003

By Vladimir E. Vigdergauz

"Bubble-mineral complexes could be formatted by an attaching of hydrophobic particles to the surface of air bubbles or by an evolution of bubbles from solution onto hydrophobic surfaces. Measurements of contact angles, detachment forces (DF), induction times (IT), evolution pressures (EP) and flotation recoveries (FR) for the studying of minerals wettability at various pH and electrochemical potentials were used. An analysis of the obtained IT results show that a process of bubble attachment to a mineral surface is a rather slow one and it will scarcely be enough for bubble-mineral complex formation under the conditions of real flotation.The ranges of adhesion potentials obtained by DF measurements, Figure 1, correlate with the data of floatability-potential for pyrite. The ranges of adhesion potentials obtained by DF measurements for galena (-1 ÷0.2V) and chalcocite (-0.5÷1.2V) correlate with the potential ranges of floatability for galena (<0.2V) and chalcocite (>-0.4V). An increase of the DF and the cathodic limit of the adhesion potential with increasing length of the hydrocarbon chain were observed. EP-pH curves for sulfides are a mirror-like to the DF-pH curves, Figure 2. Structure of solid-liquid and liquid-gas borders has a determinative importance for formation of bubble-mineral complexes and subsequently flotation results. Under vacuum on the mineral surface there are produced micro bubbles and preferably they will be appeared on the hydrophobic sites. Water structure breaks near a hydrophobic surface facilitate water mass destruction and formation of gaseous phase embryos under decompression in the impeller zone. It simultaneously reduces a probability of produced micro bubbles dissolution as a result of pressure increasing owing to constant fluctuation of liquid densities into impeller zone. Comparison of Taggart’s evaluation of the suction behind blades of the impeller of an agitation-froth machine and ABEP data on galena, Figure, shows that gas evolution will be observed in the range of 1300-2700 revolutions of impeller per minute for hydrophobic and hydrophilic surfaces successively."

Jan 1, 2003

By Tasuma Suzuki

Electrokinetic/permeable reactive barrier system is a promising in situ soil and ground water remediation technique to reduce toxic NO3- into less toxic NH4+. Using granular zero-valent iron (Fe0) as a reductant, the first objective of this study was to investigate the influence of the solid-liquid ratio and aqueouspHon NO3- reduction. The results obtained from a series of batch experiments showed that NO3- reduction was enhanced by either increasing solid-liquid ratio or decreasing aqueous pH. Based on insights obtained from batch experiments, the second objective of this study was set to design the remediation conditions of the electrokinetic/Fe0permeable reactive barrier system to maximize the NO3- reduction efficiency. Experimental results showed that the effectiveness of the system strongly depended on the Fe0 percentage in the reactive barrier, the pH in the anode reservoir, and the applied voltage, which were consistent with the results obtained from batch experiments. Under optimized treatment conditions, nearly 100 % NO3-was reduced into NH4+ in the permeable reactive barrier and collected in the cathode reservoir. Insights obtained from this study provided fundamental information on roles each of remediation design parameters plays, and will be useful to optimize the remediation conditions. Keywords: electrokinetic remediation, permeable reactive barrier, zero-valent iron, nitrate

Sep 1, 2012

By Ray Everson, Henry Kasaini

"Adsorption of Pd (II) anions on the surface of activated carbon (Norit 0.8) occurred at high proton concentration (0.01 – 2.5M, HCl) in the feed and averaged 27 mg/g. The adsorption process was interpreted in terms of surface ionisation and adsorption model. Enthalpy of adsorption averaged 0.4 kJ/mole indicative of an instantaneous physical adsorption process. We found that the Toth isotherm fit the adsorption data fairly accurately. A combination of the Langmuir and Freundlich equations yields an effective three-parameter Toth equation (1) which is frequently used to describe adsorption on heterogeneous surfaces.Figure 1 shows the comparison between experimental results and the model isotherms. We found that Langmuir isotherms underestimated the adsorption capacity on the porous surface while the Freundlich isotherm overestimated adsorption. Furthermore, the surface coverage at equilibrium was well described by both the Langmuir and Toth isotherms. But, Freundlich isotherm predicted a surface fraction coverage that was higher than unit. Based on better prediction of surface coverage and a reasonable fit to adsorption data, we concluded that the Toth isotherm best described the adsorption data of palladium. The adsorption process was limited by mass transfer resistance through the external film. We estimated the rate constant from equation (2), where e, ?b, and rp are porosity, fluid density and particle radius, respectively"

Jan 1, 2003

By K. D. Mehta

Copper concentrate containing complex sulphides of Cu-Ni with 14.13% Cu and 10.04% Ni besides impurities such as 0.33% Co and 0.71% Mo, is not acceptable to the copper smelters due to the smelting problems. Selective bioleaching of nickel from the concentrate can be considered an an option to make it suitable for copper smelter. Effect of elemental sulphur and pyrite on the bioleaching of Ni and Co has been investigated using a mixed culture of Acidithiobacillus ferrooxidans (A.f.) and Acidithiobacillus thiooxidans (A.t.). Parameters such as pH, temperature, particles, size etc. were optimised to understand the role of additives in the bioleaching. With 2% S at 308K, 2.0 pH, 5% pulp density and 200µm size particles while shaking at 100 rpm, 79% Ni, 41% Co and 5% Cu were bioleached as compared to the leaching of 81% Ni and 45% Co in presence of 10 wt% pyrite in 60 days; 27% Ni, 24% Co and 4% Cu were recovered in sterile experiment. The selective dissolution of nickel and cobalt as compared to copper may be explained by galvanic interaction between chalcopyrite: pentlandite / pyrrhotite. Bioleaching was facilitated by strong oxidizing conditions due to higher Fe3+/Fe2+ ratio/redox potential (ESCE) as a result of improved interaction of minerals through biooxidation of sulphur and accelerated galvanic interaction by pyrite. The mechanism of selective leaching of Ni and Co was established by XRD phase identification.

Sep 1, 2012

By T. Shumba

The solvent extraction section of an old Uranium Plant in the Vaal River region produced a sub-stance called Crud (Chalk River Unidentified Deposit) that formed within the aqueous/organic interface of the settler of the solvent extraction circuit. The crud was deposited together with gold tailings to the tailings dam many years ago. Previous research done on the crud confirmed that ex-posed crud leaches Mn and Ni at concentrations that are well above their acceptable risk limits as well as Zn that leaches at concentrations that are slightly lower than its acceptable risk limit. Soil washing and bioremediation technologies were employed to treat the contaminated soil. Various laboratory test work and the pilot scale studies were conducted in parallel with each other and the results of the laboratory studies were used to determine critical parameters. Four lixiviants, i.e. sulphuric acid, acetic acid, oxalic acid and ethylene diamine acetic acid were tested at three concentration levels i.e. 0.001M, 0.0001M and 0.00001M, respectively. Column tests showed that the leaching of the heavy metals increases as the soil porosity increases. Silica sand was added to increase porosity of the contaminated soil. Highest Mn removal was achieved mainly by sulphuric and oxalic acid at 0.001M at all soil levels. EDTA was significantly efficient in the removal of Ni and Zn. The recovery of heavy metals, particularly Mn, decreased as the depth of sampling in-creased. Heterogeneous bacteria and filamentous organism plate counts were conducted to evaluate the growth of the bacteria and filamentous organisms in the soil. Results showed that more organism growth took place in the bioremediated soil with a fertilizer added to it. The leaching of metals from the soil that was bioremediated in the pilot study was generally higher than the extraction of the metals from the soil that was leached with no bioremediation carried out. The results from this study suggest that the leaching of heavy metals from the contaminated soil is to a large extent dependant on the pH of the leaching solution. By increasing the soil?s porosity and bioremediating the soil, higher extractions of metals were achieved.

Jan 1, 2014

By Vishal Shukla, Ashok Kumar, Manas Ranjan, D. Chakraborty, Narayan Sharma

Jigging has a very important role in mineral processing Industry. Upgrading of Iron Ore by jigging has been an emerging trend. A detailed investigation is carried out to understand the influence of Jig feed granulometry and bed height during jigging operation. Noamundi jig plant data shows that variation in jig feed granulometry, feed quality and bed height are major contributors to fluctuation in jigging performance. At Noamundi the feed size (-10.0+0.5mm) fraction is used for fines jigging operation. To understand the effect of granulometrey on jig plant performance such as yield, separation efficiency and Fe recovery. In this context The performance of jigging was evaluated by daily average data from jig operation was used to study the influence of feed distribution on jigging performance .Coarser fraction (+6mm) has a positive influence , whereas fines fraction (-0.5mm) tends to lower performance . During Jigging rearrangements of Particles takes place due to an alternate expansion and compaction of Jig Bed .These particles are arranged by increasing density from top to bottom. During the particle stratification, Jig bed physically cut at desired horizontal particle density plant to separate the desired product. Investigation shows that optimum bed height is required at different Jig feed quality to achieve desired product quality, maximum separation efficiency and Fe recovery. This Paper will illustrate role of granulometry and Bed height control on Jigging plant performance.

Jan 1, 2014

By Kazutoshi Haga, Atsushi Shibayama, Altansukh Batnasan

"The aim of this study was to develop a hydromellurgical processing for removal of arsenic from high-arsenic copper sulfide ores and concentrates, providing increase in copper recovery. In this study, three different enargite ore samples containing 28.2–46.7% copper, 1.9–15.0% arsenic and 10.6–27.5% iron were used to determine optimum conditions for the extraction of copper and removal of arsenic. High pressure oxidative leaching process was preformed using various leaching reagents such as sulfuric acid (H2SO4), ferric sulfate (Fe2(SO4)3), hydrochloric acid (HCl), ferric chloride (FeCl3), sodium sulfate (Na2SO4), sodium chloride (NaCl) solutions and distilled water (DW), respectively, under the fixed conditions which were selected to be as follows: NaCl concentration, 0.34 M; concentrations of other leaching reagents, 0.1 M; particle size, -45 ?m; pulp density, 100 g/L; agitation speed, 750 rpm; leaching temperature, 160 ?C; leaching time, 60 min and total pressure (oxygen gas and vapor pressure) into an autoclave, 1 MPa. Results show that under the leaching conditions, more than 90% of copper leaching was achieved with lower than 2% arsenic content as a consequence of the formation of arsenic precipitates in a solution of Fe2(SO4)3–NaCl. It was determined that copper, arsenic and iron concentrations in the pregnant leach solution were 42 g/L, 0.3 g/L and 0.3 g/L, respectively. As a result, it can be concluded that the Fe2(SO4)3 solution in the presence of NaCl or FeCl3 are more efficient leaching media compared to other leaching agents under the high pressure oxidation conditions, because of their high copper recovery and lower arsenic level in the pregnant leach solution.INTRODUCTION Generally, copper is usually produced from copper sulfide ores by a combination of several processes which are flotation and smelting followed by refining [1-3]. Arsenic content in copper sulfide ores tends to increase due to the depletion of high grade copper deposits, hence conventional mineral processing and metallurgical processes cannot effectively treat these ores containing high levels of arsenic to obtain consistently high purity copper concentrates. Because high levels of arsenic in copper ores/flotation concentrates reduces the value of concentrates due to the restriction of smelting process and causes it to be a source of environmental pollution [4-6]. From this point of view, the known way of prevention against high-arsenic copper sulfide concentrates in further metallurgical treatments is to develop economically and environmentally competitive technologies for removal of arsenic impurity from copper sulfide ores before treating the ores/flotation concentrates by the pyrometallurgical routes."

Jan 1, 2018