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By N. Raeis Hosseiny, S. H. Bassir

"Chador-Malu iron ore is one of the most important iron mines of Iran.About 98 percent of Fe in the ore is in shape of Magnetite, Hematite, Martite, aqua oxide of Iron and the other irons are with ferrous silicates, actinolite, cholorite and ferrous dolomites. 1% of Fe has replaced in pyrite. The phosphor distribution in the ore is non-hemogenous and its average in the whole of the deposit is 94%. It is in shape of Apatite.This mine contains considerable phosphor, which makes it useless for metallurgical uses. At this mine the phosphor is reduced in the iron ore at two steps. At the first step, magnetic part of the ore is separated from the gangues and phosphors by magnetic separator. At the second step, the ore is enriched by the flotation methods. Experimental flotation methods to obtain the optimum conditions are as follows:• Effect of Starch as Hematite depressant with ATRAC as Apatite collector• Effect of Sodium silicate as Hematite depressant with ATRAC as Apatite collector• Effect of ASAM as Apatite collector with Sodium silicate as Hematite depressant• Effect of ATRAC (BEROL) as Apatite collector with Sodium silicate as Hematite depressant• Effect of ASAM & ATRAC mixture as Apatite collector with Sodium silicate as Hematite depressant• Effect of Kcarbonate as pH-modifier• Final test to Optimize pH, Collector, DepressantAt this research we have found the optimum circumstance of the flotation of Chador-Malu iron ore in order to decreasing phosphors of iron oxide and floating of Apatite to make pure Hematite.To reach the optimum conditions, some tests were done with different amounts of pH, collector and depressant. The results are as follows:"

Jan 1, 2003

By Grigory Voyloshnikov, Sergey Petrov, Vladimir Petrov

"The treatment of high-grade copper gold-bearing ores is practiced extensively. However, due to low concentration of copper the application of a separate process for copper recovery can make this process uneconomical. The copper, in particular: in oxide minerals, intensively bounds with cyanide during conventional cyanidation. In this case, cyanide is not able to react with precious metals and the consumption of cyanide increases. The resulting copper cyanide complexes have a negative effect on the recovery of gold. Due to decreasing of the process parameters, a repeated use of the recycled solutions can be hindered, especially in the case of heap leaching. The technology of copper removal from the process solutions with simultaneous regeneration of free cyanide from copper-cyanide complex and producing of a saleable high-grade copper concentrate was developed. An important feature of this technology is simplicity, the absence of complex or dangerous operations and the use of common reagents. The choice of equipment depends on the ore treatment option: heap or vat leaching. Also, simpler equipment schemes are available. The studies, tests and industrial practice show that if the concentration of copper can be decreased down to the first numbers of mg per ppm or lower, it is reasonable to maintain the process copper grade in the recycled solutions at 30-50 mg/L. In this case, recycling of cyanide-bearing solutions is unlimited. The regeneration of free cyanide from that of bound with copper and other cyanide complexes is 95-98%. The grade of copper in the concentrate is 55-60%. This technology is an economically competitive option, in particular: with the account of the sales of copper concentrate. The removal of copper has a positive effect on gold recovery, especially during heap leaching. In addition to, this offers significant benefits in reduced costs."

Jan 1, 2014

By Stephen J. Harker, John Knights, Randolph A. Pax, Glen A. Stewart

"Mineral samples were obtained from different stages of a mineral processing circuit used to extract the copper and gold rich mineralogical phases. The aim of this work is to characterise the quality of the samples at different stages of processing. The samples were taken of the head grade, tailings, cyclone overflow and the final concentrate.Characterisation of the samples was determined using Cu-Ka X-ray powder diffraction and Fe57 Mossbauer spectroscopy. These measurements will be presented and discussed in terms of the enrichment of the ore, showing the removal of magnetite and quartz through the processing, the final concentrate being rich in chalcopyrite and pyrite. This data also shows the utility of Mossbauer spectroscopy to provide mineralogical phase information directly.Mossbauer spectroscopy is a tool to determine the material phases of a sample. It is a nuclear based technique which measures the amount of attenuation of a narrow Doppler shifted source energy as it passes through a sample. The attenuation depends on the amount of resonantly absorbing material in the nuclear radiation path from the source to the detector. Synchronous detection of the doppler shifting velocity and the nuclear radiation count gives a Mossbauer spectrum. By convention, the energy axis of the Mossbauer spectrum is displayed in units of velocity.Figure 1 shows Mossbauer spectra obtained for a sequence of samples throughout a processing plant. These spectra show the removal of magnetite and the concentration of chalcopyrite and pyrite. Optical microscopy results indicated a significant component of bornite not witnessed with Mossbauer spectroscopy. Closer examination showed that optical microscopy assays over estimate the bornite component."

Jan 1, 2003

By M. Evertsson, K. Bhadani, E. Hulthén, M. Bengtsson

"Modelling and simulations for mineral processing plants have been successful in replicating and predicting predefined scenarios of an operating plant. However, there is a need to explore and increase the potential of such simulations to make them attractive for users. One of the tools to increase the attractiveness of the simulations is through applying optimization schemes. Optimization schemes, applied on mineral processing simulations, can identify non-intuitive solutions for a given problem. The problem definition itself is subjective in nature and is dependent on the purpose of the operating plant. The scope of this paper is to demonstrate two optimization schemes: Multi-Objective Optimization (MOO) using a Genetic Algorithm (GA) and Multi-Disciplinary Optimization (MDO) using an Individual Discipline Feasible (IDF) approach. A two stage coarse comminution plant is used as a case plant to demonstrate the applicability of the two optimization schemes. The two schemes are compared based on the problem formulations, types of result and computation time. Results show that the two optimization schemes are suitable in generating solutions to a defined problem and both schemes can be used together to produce complementary results. INTRODUCTION The comminution process for a mineral processing plant consists of multiple crushing and classification stages and aims to produce fine material to liberate ore from the minerals. The modelling and simulation of such processes are well established using static process models (King, 2001; Napier-Munn et al., 1996). A recent development in the dynamic modelling for such processes has shown further increase in fidelity compared to the static process models (Asbjörnsson, 2015). The developed simulations can be utilized to design, operate and control mineral processing plants based on the requirements of users (Bhadani et al., 2017). Typically, the requirements in the operation of the comminution process are conflicting in nature, as for instance, reduction of power draw by process units, maximization of production of fine materials, and increasing utilization of the process units. These conflicting requirements leads to a Multi-Objective Optimization (MOO) problem to operate a mineral processing plant. The MOO problems are normally referred to as non-linear problems and its fundamental understanding with respect to process behaviour is difficult to achieve."

Jan 1, 2018

By N. ??dyanik, Z. Kugukaldinova, O. Mishurina, Y. Glazkova, E. Mullina

"This paper describes the process flow of a selective processing method for acidic mine waters formed in the copper sulfide industry and characterized by a high content of copper, iron, and manganese ions. The proposed method comprises a series of sequential processes: the 1st stage is the recovery of Cu2+ ions by precipitation, the 2nd stage is the recovery of Fe2+ and Fe3+ ions as a dispersed phase by acid-base precipitation, followed by recovery in the 3rd stage of Mn2+ ions by converting Mn2+ with an oxidizing agent into insoluble forms of manganese and subsequent recovery of the dispersed phase by electroflotation. The developed method was tested on the acidic tailing storage facility (TSF) water of a mining project in the Urals region. The practical results of the implementation of the developed method have shown that its implementation will allow to recover copper, iron, and manganese in the form of salable products with a simultaneous decrease in their concentrations in adjacent water bodies down to the applicable MPCs. The process is a simple one, does not require any sophisticated expensive equipment and can be implemented either as a standalone solution or as part of existing treatment facilities. INTRODUCTION As a result of unsustainable utilization of natural resources in Russia, only a small fraction is processed into commodity products, while the rest is systematically dumped as emissions, effluents, and other wastes, polluting the environment. By amount of waste and concentration of valuable components, those wastes can be classified as aqueous technogenic resources [1, 2]. Therefore, the development of processing methods for this mineral resource category is an urgent and priority task that will significantly improve the industry’s profitability and the environmental conditions in the respective regions. MATERIALS AND METHODS Following research methods were mainly applied in this study: lab-scale and pilot-scale tests in a diaphragmless two-chamber electric flotation cell; for solutions and recoverable process products — chemical analysis using photometric determination techniques for metal cations and atomic adsorption determination techniques for the processing products. The phase composition of the precipitates formed in the process was investigated by X-ray phase analysis in the general-purpose diffractometer with a copper anode DRON-1."

Jan 1, 2018

By Cheng Gan, Gui Xiahui, Li Shulei, Cao Yijun, Liu Jiongtian, Wu Lun

Flotation rate constant is an essential parameter in the flotation process. The fine coal sample utilized in this investigation is anthracite from the Shenhuo mine in eastern China. Fine coal flotation rate tests were conducted to compare the flotation rate constant at constant power input with that at gradually increasing power input. Results indicate that the flotation rate constant decreases with the flotation process and increases as the flotation energy is increased. In addition, the flotation rate constant is close to the maximum value. The increasing trend of the flotation rate constant gradually slows down as the flotation energy input increases.

Jan 1, 2014

By R. Bugueño, W. Calderón, G. Montes-Atenas

From the point of view of industrial performance of metal extraction, the efficiency of a column leaching operation depends strongly on the leaching agent and the ore properties such as mineral composition, mineral liberation and particle size distribution. One aspect that has become particularly important is how the leaching solution flows through the porous structure which contains the valuable minerals. It is known that the output flow rate of leaching solution depends mainly on factors of the input flow, environmental condition and porous bed properties. The latter factor is often evaluated and reported under saturated conditions but in practical leaching systems unsaturated conditions are dominant. This investigation has the purpose of determining the residence time of the leaching solution in columns with different diameters under unsaturated conditions by using experimental data and numerical simulations. Laboratory leach test were performed using isothermal jacketed columns with top cap to reduce the evaporation. The simulations were performed using the software SVFlux® which incorporates material properties such as Soil Water Characteristic Curve (SWCC) and Unsaturated Hydraulic Conductivity. Preliminary results indicate a non-linear asymptotic behavior of the saturation rate with respect to the operation time. Results from numerical simulations show the same non-linear behavior and a considerable delay between input and output flows. Further analysis concerning with the effect of transpiration and evaporation mechanisms is discussed.

Jan 1, 2014

By W. X. Yin

Electrowinning of lead from aqueous solution of PbCl2 and electrowinning of manganese dioxide from aqueous solution of MnCl2 are two research focuses in hydrometallurgy. This paper investigated a new process of simultaneous electrowinning of lead and manganese dioxide in chloride medium. The simultaneous electrowinning process in chloride solution not only can prevent chloride from liberating at anodes but also obtain two electrolysis products and decrease electric energy consumption. Diaphragm cell is used in the simultaneous electrowinning process to form separate anode and cathode compartment. The effects of temperature, HCl concentration in anolyte, NaCl concentration in catholyte and electrolysis time on current efficiency and cell voltage are studied. The results indicate that current efficiency of anode and cathode for 5 hours is 99% and 96% respectively, average cell voltage is 1. 701V, the weight ratio of lead and manganese dioxide produced at electrodes is 2. 39:1 under the optimum conditions. As anode products, manganese dioxide is ??MnO2, content of which in the products is more than 92%.

Jan 1, 2014

By Kauko T. Ingerttilä, Jouko O. Kallioinen, Jaakko O. Leppinen, Alexander V. Lashkul, Vladimir E. Nenno

"Separation in Froth (SIF) is a process for the separation of mineral particles during their descent downwards through a moving froth layer, generated on the surface of water or some other liquid media by means of a bubble generator and frother. Due to the special operation principles of SIF it is possible to separate mineral particles that are about 10 times coarser than the optimal particle size for conventional flotation. In this paper the performance of the SIF technique is presented in the separation of apatite, calcite and silicate minerals from various industrial sources, based on tests with laboratory and pilot plant-scale SIF machines. Basic laboratory test results of the flotation of pure diamonds are also presented.It was shown that calcite, apatite and diamonds with particle size up to about 3 mm can be successfully floated with SIF at high recovery and grade, provided that the degree of liberation is sufficiently high. Coarse calcite (+0.25-2.8 mm) was concentrated with reverse SIF in one flotation step at 87% recovery with better than 99% grade. Apatite particles coarser than 0.2 mm are not well floated in the conventional flotation circuit leading to high P2O5 content in the coarse size fractions of flotation tailings. On the contrary, SIF is capable of recovering such coarse particles at high recovery. However, P2O5 content of the SIF tailings starts to increase at about 0.7 mm due to insufficient liberation of apatite. At higher particle size the lack of hydrophobicity of apatite particles is also likely to lower the recovery.The pilot plant testwork showed that SIF can be successfully used at operating plants not only for preliminary upgrading of the feed of conventional flotation, but also for producing final grade calcite concentrate (>99.5%) from the screen overflow or from the cyclone underflow in a particle size range up to 1 mm. It was particularly promising that the separation took place in one SIF flotation step, instead of several stages of the conventional flotation circuit, with over 90% calcite recovery. The specific capacity determined with the 1 m2 pilot plant unit was approximately 30 t/m2h. Simultaneously the consumption of chemicals was significantly lower than for conventional flotation."

Jan 1, 2003

By Y. F. Li

Fengning ilmenite ore is a magnetic deposit in gabbro containing high phosphorus and low titanium, the main minerals in which are ilmenite, magnetite and apatite. The dissemination size of magnetite is so fine that even the percentage of -0.010mm level is up to 36.50%. The fine and vein magnetite are distributed in gangue and ilmenite, so the majority of the magnetite is difficult to be separated from the gangue. Ilmenite is difficult to be recovered by low-intensity magnetic separation even through fine grinding. In high-intensity magnetic separation of ilmenite, the gangue inter-growth with the magnetite and the Fe-containing silicates may be enriched in the concentrate, and the ilmenite of the concentrate will be reduced. Based on the processing mineralogy research, combined gravity-flotation process is suggested to recover the ilmenite. The method is also good to reduce phosphorus in the ilmenite concentrate.

Jan 1, 2014

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 Nani Pajunen, Kari Heiskanen

"Products filling our societal needs, like communication and transportation needs, are becoming more sophisticated and efficient. The cost has been an increased complexity of material combinations. The same trend is also seen in investment goods. As an example, different crusher types have almost doubled the power to weight ratio in a relatively short time while producing even higher crushing rations. This has been possible by high performance materials and advanced designs. Another example is new hybrid materials in prefabricated high-strength steel structures in construction with the aim to lighten the products and obtain energy savings in the use phase e.g. in transportation. This development in general has made the end of life phase obscure. Recycling is often understood as the first phase of the material cycle. This has been supported by the material centric point of view. When, say indium, has been collected and mechanically treated to a concentrated fraction, it is assumed as recycled. This is not the case. The same applies to special steel alloys where one tends to lose some of the alloying elements to slag or even into the gas phase in the melting and refining stage, not in the earlier steps of recycling. At present there is no clear understanding of recycling of hybrid materials and no clear willingness to create new functional recycling systems. As the EU directives and most of legislation worldwide are based on the material centric thinking and implemented even on total mass recovery basis there is neither legislative incentive nor very strong economic incentives to work out the problem. In our research, we focus on industrial design towards sustainability from a product centric point of view from product collection to final metallurgical steps. It is vital, in the design phase of product, to understand the effects of decisions on recyclability to a saleable raw material. Main goal of our work is to create the fortunate circumstances in supply chain - to pass the barriers and find the effective and fruitful drivers - for reasonable use of raw materials and recycling co-operation with industry. The boundary conditions in the work are extractive metallurgical performance and the economic viability of all the steps. It can be shown from our work that small design alterations may have a large impact on the recyclability. The earlier the decisions are made in the product life chain the more positive impact they will have. It can also be shown, that a strong processing and metallurgical industry is vital to any meaningful recycling of the modern EoL products. Finally, it is also question of the individuals and values: supply and demand. Are you ready to take up the gauntlet: demand recyclable products."

Jan 1, 2014

Low-grade ore bodies, increase in rock competency, finely disseminated valuable minerals in the ore bodies, ore variability and water scarcity are among the technical challenges faced by the mining industry. These challenges have increased the business risk, capital investment and operating cost of the mining projects. Since the last 20 years, many large-scale concentrators have been built to cope with the above-mentioned challenges. Comminution, especially the fine grinding is an energy-intensive process. For example, the ball mill has a limitation in the fine grinding regime where the energy consumption increases exponentially when the product size is below 45 µm. The industry has been seeking for solutions that have a minimum risk and total cost of ownership. The stirred milling technology such as the TowerMill is well accepted by the industry as it has demonstrated the attributes required for fine grinding. TowerMill is a matured technology that has been adopted since the 80s for regrinding duty. Recently, this technology was installed in secondary and tertiary grinding duty to prepare a finer feed to rougher flotation. Four units of TowerMills were installed in a magnetite concentrator in Western Australia in tertiary grinding duty. Recently, Nippon Eirich has conducted process performance evaluation on the TowerMill circuit. The outcome of the exercise had indicated that the circuit is consuming 3.4 kWh/t to reduce from 55 µm to 35 µm with a narrow product size distribution. The effect of operating variables such as the specific energy, grinding media size, mill content % solids and mill feed configuration on the grinding efficiency were evaluated at the plant scale. Furthermore, the scale-up methodology was validated. The scope of this paper includes the performances of TowerMill and the validation of scale-up methodology.

Jan 1, 2018

By K. A. Natarajan

Involvement of various indigenous microorganisms in extracellular and intracellular iron oxide formation is a convincing index for iron ore biogenesis. Biomineralization of various iron oxides such as hematite, magnetite, goethite and limonite with the participation of aerobic and anaerobic microorganisms is well established. Various aerobic and anaerobic bacteria such as Gallionella, Leptothrix, Acidithiobacillus, Thermoplasmales, Pseudomonas, Bacillus spp and Shewanella putrefaciens, which are implicated in the formation of higher and lower oxides of iron have been isolated from different iron ore deposits. Diversity of microbial life in iron ore deposits can be put to beneficial use such as selective removal of undesirable constituents such as silica, alumina, clays, phosphorous and calcite and also to bring about environmental detoxification. Role of microorganisms such as Paenibacillus polymyxa, Bacillus subtilis, Yeasts and a sulfate reducing anaerobe in the biobeneficiation of hematite is illustrated. Surface chemical changes brought about by bacteria - iron ore mineral interactions are discussed with respect to hydrophobcity, adsorption isotherms, zeta potential data and bioreagents generation. Bacterial adaptation to minerals such as hematite, quartz, alumina, calcite, apatite and clays results in secretion of mineral ? specific biosurfactants such as proteins and polysaccharides. Such bioreagents can be used as selective collectors, dispersants and flocculants in iron ore beneficiation. Research results are highlighted to demonstrate silica, alumina, phosphate, calcite and clay removal from hematite. Environmental friendliness of such biobeneficiation processes is demonstrated with respect to biodegradation of toxic amine collectors, utility of ?in situ? organisms in enhancing settlement of fines in tailing dams and water harvesting. Keywords: bio-mineralization, bio-beneficiation, bio-remediation, Gallionella, Leptothrix

Sep 1, 2012

By Frank van der Meer, Lea Quincke

"High Pressure Grinding is applied to achieve size reduction of the particles by inter-particle breakage and to generate micro-cracks in the product particles as a contributing factor in e.g. leaching or mineral liberation. As alternative to classification, a closed circuit operation for HPGR can be established by product recycling, where a proportion of the coarser edge material and parts of the center material are split-off to be recirculated to achieve a finer final (center) discharge product for subsequent processing steps as ball mill grinding or beneficiation. As a result of the product recycling, the content of fines in the feed material increases and may affect the grinding efficiency in terms of production of fines and the generation of micro-cracks in the particles. In the scope of this paper, the effects of the proportion of fines in HPGR feed on grinding efficiency and micro-crack generation were evaluated. Grinding tests were executed with different feed size distributions, from a fines-void situation (truncated feed) to a fines-abundant situation (high product recycle). The evaluation of grinding efficiency and generation of micro-cracks was done by particle size analysis, Bond Work Index tests, impact tests on HPGR feed and products, and X-ray computed tomography of single product particles. This publication summarizes the main aspects of the outcome of these investigations."

Jan 1, 2014

By R. Van Hille, A. E. Lewis

"The precipitation of a selection of metals from both a synthetic and an actual metal-rich effluent was investigated. The experimental aspects of this study were carried out in a two-stage process consisting of a pre-treatment clarifier and a fluidised bed (pellet) reactor. Each unit operation in the two-stage process was investigated separately. The pretreatment clarification stage at pH ˜ 5 resulted in a 99.9% removal of iron and 97.3% removal of aluminium.The pellet reactor was used to precipitate nickel as nickel hydroxy-carbonate from a pure stream and a removal efficiency of 99.6% was achieved. The high local supersaturation at the reagent inlet points caused the formation of a large amount of fines, but these agglomerated onto the pellets up the length of the bed (See Figure 1).For copper precipitated as copper sulphide from a pure stream, a maximum removal efficiency of 92% was achieved. The high local supersaturation at the reagent inlets also caused the formation of a large amount of fines, but the extremely sparingly soluble nature of copper sulphide meant that the fines were not agglomerated up the length of the bed. In Figure 2, the global supersaturation ratio was relatively low, and thus there is little homogeneous nucleation and degree of fines formation. However, the fines occurring after the third sulphide input point (at 30cm from the bottom of the bed) indicate that local supersaturation also plays a critical role in fines formation. It was therefore concluded that, for the copper sulphide case, it is essential to control the supersaturation at the inlet points in order to prevent fines formation altogether, as it is not possible to agglomerate the fines once they exist in the bed."

Jan 1, 2003

By B. C. Qi

"In water treatment, flocculation or coagulation with aluminium or ferric salts has been widely used for many years to remove natural organic matter (NOM), including humic acids. However, the adsorption of NOM to aluminium hydroxide flocs during conventional coagulation/flocculation processes is very complex, with the flocculation of aluminium hydroxide particles and the adsorption of NOM molecules on flocs occurring simultaneously. Any effect on the surface characteristics and micro-structures of the humic acids and aluminium hydroxides could affect the adsorption efficiency.It has been widely observed that if a reaction system (liquid-liquid or liquid-solid) is exposed to an ultrasound field, under appropriate conditions, a variety of physical (emulsification, aggregation/flocculation) or chemical (the production of radical and exited species; single electrotransfer) actions may be activated. Though the ultrasound effects have been used in biological and chemical decontamination in many conventional environmental protection practices, the idea to explore the ultrasound effects in the removal of humic acids by preformed aluminium hydroxide flocs is relatively new. In this paper, the effect of an in-situ ultrasonication on removal of the humic acids extracted from the acidification fermentation of lignocellulosic residues, by a preformed aluminium hydroxide, was evaluated; the effect of ultrasonication on the surface complexation of the humic acids with the preformed aluminium hydroxides was investigated."

Jan 1, 2003

By Ronel du Plessis, John C. Davidtz, Jan D. Miller

Xanthates (dithiocarbonates) have been the collector of choice for the flotation of sulfide minerals ever since the flotation process was developed and have been studied quite extensively. Recently, trithiocarbonates have been shown to be very effective in bulk sulfide bench-scale flotation. Fundamental analysis using electrochemical techniques have supported these bench-scale results, illustrating that the trithiocarbonate (TTC) collectors are more readily oxidized to their corresponding dithiolates, than the dithiocarbonate (DTC) collectors, as is shown in Figure 1.

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 Heinrich Hutchison, Thomas von Moltke, Roelof F. Sandenbergh, Katarina P. Cerovic

Although the cyanidation process for gold leaching has been applied for more than a hundred years, some aspects of it, such as the passivation of the gold and the depassivating action of heavy metals, are still not well understood. In this work the anodic behaviour and surface composition of gold in alkaline aqueous cyanide with lead additions were investigated using polarization experiments and XPS. It was found that lead in the solution activated the gold at low concentrations, somewhat more positive than the reversible potential for gold, but that the activity again decreased at higher concentrations of lead. The potential range for the activation of the gold coincides with that where underpotential deposition of lead occurs, i.e. –200 to –600 mV(SCE), as indicated by the surface composition of the gold, shown in figure 1. Note that the concentration of lead on the surface of the gold only increased with time in the bulk plating potential range for lead, where gold is not activated by the presence of lead. It is also shown that up to 20 mg/L of lead added to the solution will activate the gold, provided that bulk plating of the lead is avoided. It is also important to avoid reducing conditions during leaching, where bulk plating of lead may occur, if the gold is to be activated by lead to achieve a high leaching rate, as the bulk plated lead screens the surface rather than activating it.

Jan 1, 2003