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By Graeme Lamson, Rene Dobbe, Merle Kalstrom, Janice Baron, Robert Thorpe, Chris Martin, Snezana Bajic, Amanda Palko

"This paper presents early results from a case study at the Mount Polley porphyry copper mine in British Columbia, Canada. Daily mineralogical data was acquired and reconciled with daily plant assay and recovery balances to interrogate the mineralogical controls on plant performance. After commissioning, the Minesite machine operated smoothly and reliably, creating daily data to generate mineralogical balances around the circuit for a period of several weeks. The key data, on final products were produced within 13 hours of the end of the respective operating period. The resulting information allowed for a greater understanding of the opportunities and limitations of the Mount Polley metallurgy. In this paper, how this information can be used to help long term strategic planning for the operation, as well as mine planning and production forecasting and the fine tuning of day to day mill operations is described. Early data available at the time of preparing this paper indicated that roughly 40% of the sulphide losses, or 32% of total copper losses existed as low grade inclusions in +75 micron tails. This represented the dominant form of long term copper losses, demonstrated repeatedly in the routine analytical data. However, on a day-to-day basis, the amount of copper present as chrysocolla is the major driver behind variations in total copper recovery. The degree to which this influences mill recovery is valuable to the geologist or mine planner. As they are armed with mineral speciation information for future ores, this will allow for improved mine planning, prediction of copper recoveries and production forecasting. The data was also started to find value in the mill by showing what caused sulphide losses. In the roughers, for example, the data showed poor recovery was the result of poor flotation performance and not any changes the speciation of copper sulphides or their liberation characteristics."

Jan 1, 2014

By Q. Zhang

The flotation behavior of jamesonite was investigated with ethyl xanthate as a collector. It has been shown that jamesonite has good floatability from pH 2 to pH 12, and relatively poor floata-bility at pH>12. The flotation of jamesonite was also dependent on pulp potential at certain pH val-ues. The potential-pH range for jamesonite flotation was established. The FTIR spectroscopy analy-sis and XPS measurement showed that the major adsorption product of ethyl xanthate on jamesonite was lead ethyl xanthate and antimony ethyl xanthate. The intensity of the FTIR signals of metal ethyl xanthate adsorbed on jamesonite and the flotation response of jamesonite were correlated with pulp potentials.

Jan 1, 2014

By B. Q. Xiao

In surfactant flooding, surfactants added are often a mixture of the same type of molecules with different lengths of carbon chains. The relationship between a single, pure surfactant solution and crude oil is seldom studied. Additionally, up to now, alkylbenzene sulfonates are applied widely in surfactant flooding, such as Daqing oilfield, China. A factory producing alkylbenzene sulfonates will enlarge its yield to 20 000 tons per year over there. For the purposes of widening the alkylben-zene sulfonates? application, 16 kinds of pure alkylbenzene sulfonates were synthesized through Friedel-Crafts acylation and Wolff-Kishner reduction reactions, and the compounds? molecular structures were confirmed by 1HNMR and 13CNMR spectra. The factors affecting interfacial tension (IFT), such as, surfactant type, oil composition, electrolyte concentration, and alkali concentration were considered. The synthesized pure surfactants? critical micelle concentration (CMC) and optimal salinity were measured through interfacial tension technique. According to lab experiments results, heavy alkylbenzene sulfonate (2SY) was synthesized in magnifying scale in Jinzhou Wash Chemical Plant and the coretests were conducted using it. The results showed that the homemade heavy alkylbenzene sulfonate (2SY) flooding can improve oil displacement efficiency 20% more than water flooding at surfactant?s concentration from 0.05%(wt) to 0.2 %(wt).

Jan 1, 2014

By Y. H. Zhang

Mechanism of BK501 in desiliconization from bauxite was studied by use of flotation test, EDS, ?-potential, FTIR. Results of flotation show that almost all of diaspore can be depressed when BK501 is put into pulp ranging from pH 4~12, in the meanwhile kaolinite is slightly activated. In the light of surface analyses, it is concluded that the adsorption of reagent on the diaspore is dominant by chemical interaction. Moreover, kaolinite may float more by addition of BK501 because of flocculation.

Jan 1, 2014

By J. J. Cai

The status of fossil fuel and secondary resource in metallurgy industry in China were reviewed, and conversion efficiency of fossil fuel, utilization technologies of secondary energy were studied. Fossil fuel, accounting for over 90% of energy structure in metallurgy industry, took in the highest flight in China, and a great deal of which was converted to secondary energy through the equipment of blast furnace and coke oven. These secondary energy which were mostly made of blast furnace gas(BFG), coke oven gas(COG) and Lindz Donawitz gas(LDG) occupied about 30% of total secondary energy. The way enhancing fossil fuel conversion efficiency, secondary resource recovery and the secondary energy such as BFG, COG, LDG utilization promoted to save fossil fuel was discussed in this paper. And efficient use of lower caloric value fuel was studied, such as preheating combustion air and fuel, generating electricity power etc. and regeneration purposes of high-caloric fuel was also researched, for producing hydrogen, methanol or direct reduction iron etc. The using model of secondary energy at iron and steel works was presented as fuel and chemical materials. The results suggest that utilization of these energy efficiently and reasonably could help to energy saving and environment protecting.

Jan 1, 2014

By R. K. Rath

The low-grade iron ore sample contains both lumps and fines. It is mostly hematitic iron ore and considerable amount of goethitic/limonitic material is present in it. The major impurities present were quartz and clay. It is observed that the iron bearing phases are poorly liberated above 300 µm and the liberation improves below 300 µm. More than 80% liberation is achieved below 106 µm. Based on the liberation data, the feed for the different beneficiation methods was prepared by stage crushed the ROM followed by grinding passing to 106µm and the ground material (-106µm) was deslimed. The underflow was subjected to various beneficiation techniques such as tabling, enhanced gravity separator (EGS), wet high intensity magnetic separation (WHIMS), and flotation and the results are discussed. All the methods studied could able to produce pellet grade concentrate with iron content of 64.5%, however, a marginal higher yield was observed for WHIMS (81%). Keywords: beneficiation, gravity, magnetic, enhanced gravity separation, flotation, low-grade iron ore, desliming

Sep 1, 2012

By M. Kargar Razi

According to the unique properties and many applications of nano silver powder, it was prepared from acid leaching tail solution. The low value residual gold and silver ions were occurred with fellow heavy metals as pollutants (Fe2+, Cu 2+and Zn2+) in acid leaching tail solution in Mouteh gold mine in Iran. Preparation of nano silver particles was achieved in two steps: first, by addition of ammonia as separation step and second by using different reagents as precipitation and extraction steps. Different controlled parameters were including pH, residence time and temperature, mixing time, and reducing reagents to metals molar ratio. Acid leaching process was carried out with sulphuric and nitric acid via suitable reductants. In order to remove copper, zinc, and silver ions from solution, all of the conditions were controlled. The optimum conditions for preparation of nano silver powder with less than 90 nm were pH 10.5, hydrazine/methanol to silver molar ratio of 3 to 4, and reduction time of 5 min in 45 °C. The results were evaluated via SEM, A.A and UV- Vis spectroscopy analytical methods.

Jan 1, 2014

The effect of the acid anion on chalcopyrite (CuFeS2) leaching has been examined, under care-fully controlled conditions, in a range of acids in stirred reactors and columns at pH 1. Solution speciation calculations were performed to determine possible rate controlling species. The relative leach rates of Cu from chalcopyrite can be explained quantitatively entirely on the basis of solution speciation without the need to invoke any rational relating to surface structure/speciation. The rate of Cu release is first order with respect to Fe3+ activity. The stirred batch reactor experiments at fixed pH 1, Eh of 750 mV (SHE) and 75? showed that chalcopyrite leach rates were rapid in both HClO4 and H2SO4 with 100 % Cu recovery after 73h and 97 h respectively. However, the leach rate in H2SO4 was slower as compared to the HClO4 leach due to a slower increase in the activity of Fe3+ due to the formation of FeSO4-. The presence of Cl- in the leaches (HCl and H2SO4 with NaCl added) led to a low activity of Fe3+, due to the high activity of FeCl2+, resulting in very low leach rates. For the column leach experiments dissolution of Fe and Cu from the pH 1 HCl eluted chalcopy-rite column with quartz proceeded at several times the rate of any other column (chalcopyrite with and without quartz and/or pyrite leached with H2SO4, HClO4, HCl). Three observations indicate that galvanic interactions are not leach rate controlling role: a) The rate of leaching was not uniformly increased for the non-quartz containing columns where the two sulfide minerals, chalcopyrite and pyrite, are in physical contact as compared to the analogous quartz containing columns where they are not; b) there exists a reasonable correlation between the rate of Cu release and the effluent Fe3+ activity for all columns thus indicating that the leach rate is determined by solution speciation; and c) in all cases the proportion of Fe to Cu leached indicates preferential dissolution of Cu over Fe. However, the proportion of Fe to Cu is either the same or greater than expected on the basis of the single mineral columns. This indicates that chalcopyrite is not dissolving preferentially to pyrite.

Jan 1, 2014

By Liu Jie

Refractory iron ore deposits in China have various genesis and complicated types, the nature of which is poor, fine-disseminated and complex. Therefore, refractory iron ore could scarcely be separated and utilized by traditional mineral processing technology at present. It is necessary to explore deep reduction technology to change the characteristics of refractory iron ore and to use effectively the iron resource. And deep reduction technology is that on the condition of higher reduction temperature than that of magnetic roasting and stronger reducing atmosphere, the iron oxides from iron ore was reduced to metallic iron particle that is easy to dissociate. And then production from deep reduction is easily separated by magnetic separation and iron powder production was obtained finally. Deep reduction technology for Lingyang iron ore from Jilin, China, as the refractory iron ore, was studied in this paper. The influences of such main factors as reduction temperature, time and coal content were investigated. The results showed that the Metallization rate of reduction product was up to more than 90% under optimum conditions, and then higher iron grade and recovery of reduction iron powder were obtained from subsequent magnetic separation. Furthermore, the deep reduction mechanism in the system was studied by the means of XRD and SEM analysis for reduction production and Physical Chemistry of Metallurgy. Analytical results indicated that during deep reduction, the size of iron particle from deep reduction materials was increasing as reduction temperature rising and reduction time extending. The growth of metallic iron particle from deep reduction production was divided into such three stages as reduction nucleation, deep reduction and growth of metallic iron particle.

Sep 1, 2012

By Evvie Chockalingam

Acid mine drainage (AMD) is a perennial problem particularly in abandoned mines, occurring due to the oxidation of sulphidic mine wastes. AMD is usually characterized by high concentration of dissolved metal ions, sulphate and low pH. The efficacies of substrates such as rice husk and the bark of Eucalyptus tereticornis (Sm.) are assessed for the removal of metal ions such as iron, zinc and copper from acid mine water obtained from an abandoned copper mine. Over 99 % of Fe, 98 % of Zn and 95 % of Cu removal could be achieved from acid mine water, with a concomitant increase in the pH value by three units using rice husk as an adsorbent. With respect to tree bark as an adsor-bent, about 96 % of Fe, 75 % of Zn and 92 % of Cu could be removed from the acid mine water with an attendant increase in the pH value by two units. The free energy of adsorption of the metal ions onto rice husk and tree bark is found to be negative in both the cases, while the adsorption process is endothermic in the case of rice husk and exothermic for tree bark. The adsorption process is found to adhere to the Lagergren pseudo-first order rate equation. The reduction of sulphate con-centration in the acid mine water is achieved using a typical sulphate reducing bacteria namely De-sulfotomaculum nigrificans. Desorption experiments indicate that about 88 % of Zn, 87% of Cu and over 77 % of Fe could be recovered from rice husk and over 70 % of Fe, 82 % of Zn and 77 % of Cu could be desorbed from the metal loaded tree bark using 5 M HCl. The possible mechanisms of metal ion and sulphate removal from acid mine water using rice husk and tree bark are discussed.

Jan 1, 2014

By C. Abbruzzese, F. Vegliò, S. Ubaldini, R. Massidda

"Gold solubilised during cyanidation can be recovered by precipitation (Merrill-Crow process) or by adsorption onto activated carbon, these being the techniques applied in industrial plants.Precious metals (Au, Ag) adsorbed onto activated carbon are extracted during a subsequent stage in aqueous phase, by various technologies, such as hot elution (70-80°C) or under pression desorption (100-130°), with hydro-alcoholic solutions.This stage is of great interest from an economic point of view, due to the high energy costs. Temperature represents the critical kinetic factor.The aim of this paper was to study the influence of different water/organic solvent mixtures (isopropyl alcohol, ethanol and ethylene glycol) on the desorption process.The experimental work was carried out on laboratory scale, using activated coconut carbon with different temperatures and extraction times, without adding cyanide.Best results have been obtained in this order: isopropyl alcohol > ethylene glycol > ethanol. Starting from gold concentration of about 5 g Au per kg of carbon, best kinetics resulted in 97-100% of gold extraction, after 8 hours of desorption, at a temperature of 80ºC."

Jan 1, 2003

By S. Leroy

Grinding is the most energy consuming step in mineral processing, however, it is still poorly understood and its efficiency is difficult to monitor. Mill performances are traditionally measured at the mill discharge, on the basis of a mass percentage passing a certain sieve. This approach does not reflect what happens to the fines through milling. On another hand, if many macroscopic parameters, such as the percent solids of the pulp, its viscosity, or its mean residence time in the mill are known to be related to grinding efficiency, the link between these parameters and particle size distribution (PSD) is still unclear. Here, a methodology is established to understand the effect of ball mill operating conditions on particle size and shape distribution in the grinding process. The study focuses on the particular case of an Upper Group 2 (UG-2) platinum ore concentrator. Due to the very low grade of sulphide and PGM (Platinum group metals) in UG-2, grinding mechanisms are entirely control by gangue minerals. These two minerals have contrasted properties and PGM content and these properties immediately affect the entire recovery process. So, the grinding of both gangue minerals is studied on a size by size basis. At particle scale, three parameters are addressed: particle size, particle composition and particle shape. The specific behavior of chromite and silicate grains is demonstrated. As a conclusion, this study gives some clues to operate ball mills in a more efficient manner regarding chromite issue in the processing of UG-2. Keywords: ball milling control, UG-2, chromite, fine particle, particle shape, segregation

Sep 1, 2012

By Z. Q. Zhang

The iron ore from Yichang in China assaying 41.64% Fe and 1.02% P is a low grade and high phosphorus oolitic hematite ore. The separation of iron minerals from gangue minerals in the ore by conventional processing techniques is ineffective owing to their close similar properties. The modification of iron minerals by microwave-assisted reduction was investigated in order to improve separability of the ore. The effects of microwave-assisted reduction on the subsequent low intensity magnetic separation and floatation were examined. The results show that the main factors affecting the reduction and separation process are grinding size, reduction temperature and reductant. Fine grinding of the microwave-treated ore to smaller than 0.074mm was found to be imperative due to the tiny dissemination characteristics of iron oxide minerals. After magnetizing reduction by microwave heating at 500?, the magnetic concentrate containing 58.36% Fe and 0.67% P can be obtained with the Fe recovery of 91.28%. Magnetizing reduction drops the floatability of iron oxide minerals, thus reverse flotation is fit for upgrading the magnetic concentrate to contain 62.13% Fe and 0.21% P with Fe recovery of 81.59%. Compared with present microwave-assisted reduction technique of carbon reductant, using a waste iron powder as reductant is a novel and effective technique without the green house effect caused by the release of CO and CO2. Waste iron powder with a faster response to microwave heating then coke and charcoal can be recovered by magnetic separation in a low cost and plays the role of reductant and microwave heating accelerator.

Jan 1, 2014

By K. C. Corin, M. S. Manono, R. M. Manenzhe, J. G. Wiese

"Environmental concerns necessitate the recycling of process water within mining operations. Given that recycled water is chemically different from fresh water, and collectors are added such that they adsorb at the liquid-particle interface, changes in the aqueous phase are expected to affect collector adsorption. A Finnish nickel-copper ore was floated in synthetic plant waters of varying ionic strengths and plant waters obtained at Boliden Kevitsa Mine, with aerophine and sodium isopropyl xanthate as collectors. Of the tested waters, the copper thickener overflow was the least conducive to xanthate adsorption and valuable mineral recovery. The nickel thickener overflow, standard process water, and raw water were the most conducive to xanthate adsorption. For the raw water and nickel thickener overflow, increased adsorption correlated with increased valuable mineral recovery. Further, recycling xanthate retained in water affected the selectivity of the collector and hence the concentrate grades.INTRODUCTIONFlotation is a separation process that exploits the differences in the surface properties of the particles being separated. The efficiency of separation is dependent on the degree of hydrophobicity achieved by the particles meant to be floated, which are, in most cases, valuable minerals. The hydrophobicity is in turn dependent on the adsorption of the chosen collector onto the surfaces of the floated particles (Fuerstenau, 1984; Taggart and Hassialis, 1946). Empirical findings suggest that species dissolved in solution strongly influence collector adsorption and overall flotation response (Fuerstenau and Chander, 1986). Due to environmental concerns, it is becoming more pertinent for mining plants to recycle process water and hence limit the usage of potable water. There is an interest to ensure minimal discharge of plant water into the environment, as this water is typically polluted with process reagents that may render it toxic (Levay et al., 2001)."

Jan 1, 2018

By D. Tao

A novel rotary triboelectrostatic separator has been developed and patented recently at the University of Kentucky with unique features, including a high efficiency rotary charger, charger electrification, laminar air flow, etc. A parametric study has been performed with a coal combustion fly ash sample to investigate the effects of major operating parameters on the process performance. Most significant operating variables and optimum conditions were identified. Separation tests performed with four fly ash samples indicated that the rotary triboelectrostatic separator showed effective fly ash separation.

Jan 1, 2014

The flotation behavior of kaolinite and diaspore using N, N-diethyl dodecyl amine (DEN12) and N, N-dimethyl dodecyl amine (DRN12) as collector have been investigated through flotation experiments. The mechanism of adsorption of two tertiary amine collectors on surface of kaolinite and diaspore were investigated by FTIR spectral, Zeta potentials measurements and calculation of molecular orbital energy. It has been found that DEN12 and DRN12 have stronger collecting power to kaolinite and weaker collecting abilityto diaspore than DDA. Kaolinite and diaspore in bauxite ores can be separated by using DEN12 and DRN12 as collectors at pulp pH below 8 and 6, respectively. The results of zeta potentials and calculation of molecular orbital energy indicated that the adsorption strength on kaolinite surface is in the order DEN12>DRN12>DDA and the adsorption strength on diaspore surface is in the order DDA>DEN12>DRN12. FTIR spectral analysis and Zeta potentials approve that the action between kaolinite and tertiary amine collector is strong electrostatic adsorption and that of diaspore is weak electrostatic adsorption in the range of pH 5~6.

Jan 1, 2014

Cyanide is reactive to copper minerals and is not suitable to extract the gold from the copper bearing ores. Ammoniacal thiosulfate is considered an excellent alternative lixiviant for leaching copper bearing gold ores. Unfortunately the results of high reagent consumption and poor gold ex-traction were found by thiosulfate leaching of synthetic gold ores containing chalcopyrite, chalcocite or bornite and a mild refractory copper-bearing sulfidic gold ore. In this investigation, several processes have been applied to reduce the impacts of these minerals on gold leaching. The process included: the pre-oxidation of copper sulphide minerals in water or ammonia solution, the reduction of dissolved oxygen in the lixiviant (0.3 ppm DO or 0.7% oxygen), adding phosphate anion in the leach or pre-leach stage, and the addition of a strong copper ligand (e.g., EDA and DETA). The results indicated that the gold extraction could be improved to 93% with the thiosulfate consumption being reduced to less than 8 kg/t. The dissolution of copper minerals was found to be the major reason for increased consumption of thiosulfate and the highly reductive leached surfaces are responsible for the reduced gold extractions.

Jan 1, 2014

By T. Bhambhani, O. Yavuzkan, D. R. Nagaraj

"The recovery of oxide Cu minerals by flotation is a longstanding challenge in the minerals industry, especially for high acid-consuming ores which would not be economical for direct acid leaching. Sulfidization (often using controlled potential sulfidization or CPS) using NaSH (or Na2S) followed by flotation using traditional sulfide collectors is the widely used technique. CPS has certain limitations: a) inability to recover certain oxide Cu minerals because they are refractory to sulfidization, b) high consumption of NaSH (or Na2S), and c) potential health and safety hazards associated with NaSH (and Na2S). Flotation of oxide copper minerals using alkyl hydroxamate (AHX) collector has been studied extensively. Investigations using single minerals and laboratory ore flotation have been conducted in the past to demonstrate the efficacy of alkyl hydroxamates. The technology has been used intermittently in plants. One of the main challenges in plant use has been quantifying the true potential for alkyl hydroxamates for recovery of various oxide Cu species in complex and variable ore systems and identifying the most suitable conditions for optimal use. Quantitative mineralogical analysis using QEMSCAN was used in this study to characterize flotation products lab flotation samples. Analysis of concentrates and tails from hydroxamate flotation and CPS flotation stages demonstrated that certain oxide Cu minerals respond exclusively to alkyl hydroxamates and not to CPS. The hierarchy of interaction of AHX with the various oxide Cu minerals could be inferred from these studies. Finally, these studies also allowed quantification of a group of minerals species, which (erroneously) report as part of the Acid-Soluble Cu [ASCu] but cannot be recovered by flotation, thereby facilitating an estimation of the true recovery potential for alkyl hydroxamate.INTRODUCTIONCopper that is economically recoverable occurs in three major types of ores, which are defined by the modal mineralogy of Cu. For sulfide ores, Cu occurs as sulfide minerals and is satisfactorily recovered by flotation using sulfide collectors. Non-sulfide ores, which contain Cu in the form of oxides, phosphates, carbonates and silicates, described in the industry as “oxide” ores (or ores containing “acid-soluble” Cu or ASCu), are currently treated using hydrometallurgy, which involves leaching with dilute sulfuric acid followed by solvent extraction and electrowinning, unless the ores contain acid consuming gangue minerals such as dolomite. For mixed sulfide-oxide ores (i.e. containing both sulfide and oxide Cu minerals) that do not contain acid consuming gangue minerals, Cu values are easily recovered by flotation of sulfide Cu minerals followed by leaching of oxides (only when a leach plant is available). However, when the ore contains acid consuming gangue minerals flotation is required to recover both sulfide and oxide Cu minerals."

Jan 1, 2018

By S. Koca

Vast amount of fly ash, bottom ash and slags, are produced each year due to coal combustion in thermal power plants. These products consist of mainly unburned carbon and inorganic compound (such as: silica, alumina, iron oxides, magnesium oxide, phosphorus oxide etc.). These are valuable minerals and can be recycled or recovered if properly processed. One third of the material find application as an ingredient in cement and other construction products, the rest is held in dams or similar dumps, which results in a hazardous impact on the environment, polluting soil and ground water. The unproductive use of land, the associated long term financial burden maintenance and negative environmental impacts have led to realization that alternative uses for combustion by-products as a value added product beyond incorporation in construction materials are needed. At present, there is an intensive search to increase their uses. Other uses of coal combustion residues include as raw material in brick and ceramic tile fabrication, as filler in plastics and paints, extraction of valuable mineral materials, production of zeolites and soil and mine waste treatments. Separation of unburned carbon from bottom ashes by means of flotation was conducted in order to increase the possibility of the recycling of coal combustion wastes. In the flotation experiments collector, dispersant and frother amount, pulp density and pH were tested as variables. After first stage flotation experiments, at optimum conditions, the carbon content was reduced down to 5.58 % in the tailings fraction. This fraction meets the industrial specifications and can be utilized as a cement additive. At the same conditions the carbon content of the concentrate increased to 44.72 % at a carbon recovery of 65.81 %. After the cleaner stage flotation experiment the carbon content of the product is enhanced to 62.53 %. This fraction can be blended back into the coal feed to the power plant boilers.

Jan 1, 2014

By L. E. Veki, S. M. Luukkanen, J. P. Karvonen, J. O. Leppinen

Today there is a consensus that xanthate adsorption on sulfide minerals is primarily controlled by redox reactions occurring at specific potentials on these semi-conductive minerals. Consequently, it is possible to control xanthate adsorption by controlling electrochemical conditions in the system by using oxidizing and reducing agents. The scope of this study was to investigate the possibilities to increase the selectivity of Cu-Fe-Zn ore flotation by applying electrochemical control in the conditioning of the flotation feed. In this work, mild steel grinding in a nitrogen atmosphere was used as the basis to provide a negative starting potential and minimize the amount of oxidation products on sulfide mineral surfaces. To study how different potential levels affect flotation results, a controlled conditioning procedure was utilized maintaining potential at a desired level by titrating the pulp with air. Xanthate adsorption kinetics during conditioning was examined by taking pulp samples for spectrophotometric analysis and laboratory flotation tests were conducted for samples that underwent the controlled conditioning procedure in the potential range of -200mV to +200mV vs. SHE. A clear correlation was detected between chalcopyrite recovery and the potential during controlled conditioning indicating that there was a constant increase in chalcopyrite recovery when the potential was shifted to more anodic values. It is possible that utilizing potential control in the conditioning stage, a smelter grade copper concentrate can be achieved directly in rougher flotation without cleaning stages. Conditioning in favorable conditions had significant positive effects on flotation selectivity of chalcopyrite. The improvement in copper concentrate grade being predominantly caused by the depression of pyrite. By applying the controlled conditioning procedure pyrite recovery in rougher flotation was reduced even low as under 1%, while in the tests without controlled conditioning, pyrite recovery varied between 7.5 – 65.7%. The result of this work indicate that affecting collector adsorption by electrochemical control in the conditioning stage can provide significant improvement in sulfide mineral flotation and industrial applications could lead to decreased chemical consumption, reduced equipment and maintenance costs.

Jan 1, 2018