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By S. M. Bradshaw, C. Dorfling, F. Ngandu

"Selenium removal and platinum group metal (PGM) recovery from copper sulfate leach solutions form an integral part of platinum producers’ base metal refinery operations. Recent studies found that substantially higher PGM recoveries can be achieved if excess thiourea instead of sulfurous acid is used as precipitation reagent; however, the impact of the proposed process on downstream processes was unknown. The objective of the current study was therefore to investigate the effects that excess thiourea and residual selenium present in the rich copper sulfate electrolyte have on copper electrowinning. This was achieved by performing cyclic voltammetry tests using a platinum rotating disk as working electrode, a graphite auxiliary electrode and a saturated calomel reference electrode. A synthetic copper sulfate electrolyte containing 0.01 M Cu2+, 1 M H2SO4 and varying amounts of selenium (20 – 150 mg/L) and thiourea (10 mg/L and 100 – 300 % excess) was used. The results obtained have shown that both thiourea and selenium interact with the cupric ion cathodic reduction reaction. Thiourea polarized the working electrode and lowered the efficiency of the cupric reduction reaction. Tests on the solutions with high selenium concentration showed simultaneous reduction of copper and selenium, which led to copper selenide formation. Nodule formation on the deposit surface also became significant at higher selenium concentrations. Based on these results, it was concluded that precipitation of PGMs from the copper sulfate solution with excess thiourea is not feasible due to the detrimental effect on downstream electrowinning operations.INTRODUCTION During the high pressure oxidative leaching stage in a typical base metal refinery (BMR) circuit, selenium, tellurium and some platinum group metals (PGMs) are dissolved along with the desired copper ions. The impurities (selenium and tellurium) may pass to the copper electrowinning circuit where it can result in the formation of nodular copper electrodeposits or reduced current efficiency. The presence of PGMs in solution, on the other hand, increases the precious metal inventory and potential losses of the operation. Currently, sulfurous acid is widely used for selenium and tellurium precipitation from copper sulfate leach solutions. Sulfurous acid is capable of reducing cupric ions to cuprous ions; the generated cuprous ions then react with Se4+ and Se6+ to precipitate selenium as a copper selenide (Bello, Dorfling, 2014). Recent studies have, however, proposed the use of excess thiourea as a precipitating agent for the removal of selenium and tellurium; it has the advantage of improved PGM recovery in the Se/Te precipitation step (Lottering, Eksteen et al., 2012; Mulwanda, Dorfling, 2015)."

Jan 1, 2018

By Zoran M. Stevic, Mirjana M. Rajcic-Vujasinovic, Zvonimir D. Stankovic

"Covellite is one of the most important copper sulfide minerals. Its behavior during the anodic polarization, as well as its rest potential in various solutions are of importance for flotation processes and also define the mechanism of electrochemical extraction of copper from sulfide minerals.Measurements of the rest potential have been performed in water solutions in presence of different cations and anions. The existence of the Nernst type dependence of the rest potential on the activity of some of the investigated ions was established. The biggest influence on the rest potential of covellite exhibits the change of activities of the ions forming the crystal lattice of investigated mineral, i.e. Cu(II) and S(II). The dependence of the rest potential of covellite on logarithm of Cu(II) activity has a shape of a strait line with a positive slope of 60 mV, while when concentration of S(II) anions increases ten times, the rest potential of covellite decreases about 120 mV. The first dependence was established in acid medium, while the second was registered in alkali one.Different electrochemical techniques have been used for the investigation of the behavior of covellite during anodic polarization. In the basis of all these measurements is a three electrode system consisted of: 1) working electrode made of the sample of natural covellite from the Bor mine (Eastern Serbia, Yugoslavia); 2) reference electrode (saturated calomel electrode) and 3) counter electrode (flat platinum). Electrolyte solutions used in these investigations are of the same kind as those used in the rest potential measurements. Sulfate and chloride solutions, as well as the mixed sulfate/chloride solutions, are the most perspective from the application point of view.Cyclic voltammetry has been the first used method that confirmed the formation of passive layer on the electrode surface during anodic polarization. Elementary data about the reaction mechanism have been obtained too. More detailed data needed for more precise conclusions about the mechanism and rate of the anodic process on covellite have been obtained by galvanostatic method. It was established that the essential difference exists between the reaction mechanism in sulfate and chloride solutions. Also, the difference is exhibited in the nature of reaction product directly connected with the passivation of the electrode surface. Chronopotentiometric investigations have been performed in sulfate, nitrate, chloride perchlorate and mixed sulfate/chloride solutions applying different current densities. The shape of obtained curves indicate if there was a surface passivation and how intensive it was."

Jan 1, 2003

By Markus A. Reuter, Joep Verwoerd, Marc J. A. Pijnenborg, Yongxiang Yang

"Incineration is a proven disposal technology for all waste materials with heat release potentials, and provides high degree of toxic destruction and control for a broad range of hazardous materials. In the Netherlands, all the hazardous wastes are processed at AVR-Chemie located at the Rotterdam harbour, through rotary kiln incinerators. The newly enforced regulations from the European Union with stricter emission levels require a better understanding of the incineration process and improved process control. However, the transport phenomena and combustion processes within the kiln system are very complex and not well understood. In order to get better understanding of the incineration process, research has been carried out to study the fluid flow and combustion behaviour of the incineration system. Computational Fluid-dynamics (CFD) was used to simulate the gas flow and waste combustion process, and temperature measurements of the operating rotary kiln incinerator were conducted to validate the CFD model. This paper will present the latest results from the current research project for simulating gas flow and combustion heat transfer for a wide range of hazardous waste streams.The simulation of the waste incineration process was carried out using a general-purpose CFD code Phoenics. The rotary kiln and the secondary combustion chamber (SCC), with a waste processing capacity of 50,000 ton/y and an energy input of 30 – 40 MW, is translated into a CFD model. The model includes a k-e turbulence model and a global gas-phase combustion model (3-gas or 7-gas combustion model). The 3- gas model (Simple Chemically-Reacting System, SCRS) predicts only the thermal effect of the fuel combustion, and only one global fuel is used, therefore, real chemical species are not taken into account. In the 7-gas combustion model, (an Extended SCRS, ESCRS), different forms of waste fed into the incinerator have been modelled into a mixture of a general hydrocarbon fuel C3H4 and other components such as CO, CO2 and H2O. Thus, all the incoming fuel streams with different compositions and calorific values can be properly converted into separate inlets. The combustion of the waste is assumed to take place only in gas phase in two steps: (1) primary combustion of the main fuel component C3H4 to form CO and H2, (2) secondary combustion of CO and H2O to form CO2 and H2O. The rate of each combustion reaction is assumed to be controlled by turbulent mixing of fuel and oxidant (air or oxygen), i.e. the Eddy-Break-up (EBU) model. The resulted temperature field was validated with temperature measurement data, and the simulated temperature distribution from both 3-gas and 7-gas model have reasonable agreement with the measured data."

Jan 1, 2003

By S. A. Vorobyev, Yu. L. Mikhlin, Ye. V. Tomashevich, A. A. Karacharov, M. N. Likhatski1, A. S. Romanchenko, S. V. Saikova

"A set of state-of-the-art methods have been applied to study ultrafine particles and nanoscale species arising on mineral surfaces upon milling, interaction with flotation reagents, and leaching of base metal sulfide ores in order to gain insights into interfacial mechanisms. The fine fractions produced by ball milling of a Pb-Zn Gorevsky ore and four Cu-Ni sulfide ores studied with laser diffraction, dynamic light scattering, zeta-potential measurement, Xray photoelectron spectroscopy (XPS), SEM, TEM and other techniques. The particle size distributions had, aside from the peaks at 20-60 ?m, maxima near 1-2 ?m; the flotation was considerably suppressed when the yield of positively charged ultrafine particles approached tenths % (several kg per ton). High-energy XPS and X-ray absorption spectra revealed that sulfide minerals depleted in metal in air and aqueous solutions were composed of outer “polysulfide” layers, strata with disulfide species, and heavily defective underlayers, and “passivation” was explained by stability of the metal-deficit structures. Dixanthogen at pyrite and copper-activated sphalerite, dixanthogen and then cuprous xanthate on chalcopyrite, and chemisorbed xanthate at galena were specified as the main interfacial products using cryo-XPS of fast-frozen flotation slurries. The particle size, zeta-potential and behavior of colloids of Cu and Pb xanthates and dixanthogens were largely determined by the initial ratio of a cation and collector; the properties of copper xanthate nanoparticles were also affected by incorporated dixanthogen (about 15 wt.%). Submicrometer gas domains of 3-8 nm in height and “hydrophobic” forces upon the probe retraction were found on xanthate-treated minerals using atomic force microscopy and spectroscopy; their impact on flotation is briefly discussed.INTRODUCTIONInterfacial phenomena play a key role in flotation, leaching, water purification and related environmental processes. The mineral processing and extraction of metal from sulfide ores commonly involves milling the ore, which produces, along with the particles of 20 µm to 100 µm, mineral entities ranging from micrometer to submicrometer and nanometer scale. Furthermore, ultrafine particles of flotation reagents, products of metal sulfide oxidation, and so on may form spontaneously and accumulate in production water, flotation froth, deposit on mineral surfaces, affecting the flotation performance, and then enter waste waters, mine and natural drainage, polluting soils, surface- and ground waters (Miettinen et al., 2010; Wang et al., 2014). The efficiency of flotation and hydrometallurgical recovery of values, environmental issues are crucially dependent on the state of mineral surfaces. Particularly, it is generally accepted that the surface non-stoichiometry of sulfide minerals induced by oxidation and leaching should affect their hydrophobicity and reactivity, including so-called “passivation”, but the nature of such surface layers are still a matter of controversy (see, for example, Holmes and Crundwell, 2013). Another phenomenon attracting rapidly growing interest in several areas is low-dimensional gas species (“nanobubbles”) at hydrophobic surfaces that may play a decisive role in particle-bubble attachment in flotation but remains scarcely investigated up to now (Xing et al., 2017). Here, we survey our recent results on the abovementioned problems applying a series of rather new methods and approaches; more details can be found in refs. Karacharov et al., 2016; Mikhlin et al., 2015; 2016; 2016a; 2016b; 2016c; 2016d; 2017; 2017a; Vorobyev et al., 2017."

Jan 1, 2018

By Vincent C. Smith, Agit Singh, Bernard Muller

The control of minerals processing plants is by no means trivial. In order to address some of the difficulties, it was decided to develop and test a model predictive controller (MPC) for a milling circuit. A milling simulator was written to test the MPC controller. Due to the large number of tuning parameters in a controller of this type, an optimising algorithm was written that automatically tunes the controller. Good, robust control was obtained when the controller was tuned using this algorithm. The controller was tested for various scenarios that are often encountered in the minerals processing industry. When problems were encountered, the MPC algorithm was specially adapted to accommodate for these difficulties. Control was further improved by using feedforward control as well as quadratic programming. The movement of the manipulated variables was reduced by using a region of uncertainty that allows the controlled variable to vary within a specified region around the setpoint. Integrators were handled by adapting the algorithm slightly and adding an optional integral error portion in the MPC controller. The performance of the enhanced MPC controller was compared to PI controllers on both the simulator and a commercial plant. The MPC controller showed faster responses with less interaction in both cases.

Jan 1, 2003

By Naoki Hiroyoshi, Hajime Miki, Tsuyoshi Hirajima, Masami Tsunekawa

Acidic solutions for chalcopyrite leaching contain cupric, ferrous and ferric ions, and the oxidizing power of the solutions is indicated by a redox potential, determined by the concentration ratio of ferric to ferrous ions. This paper reviews our previous studies on the redox potential dependence of chalcopyrite leaching in sulfuric acid solutions. Leaching and anodic-polarization experiments showed that coexistence of cupric and ferrous ions activate anodic dissolution of chalcopyrite, causing faster copper extraction at the potentials below a certain value (critical potential). The analysis of the AC impedance spectra for chalcopyrite electrode indicated that a high-resistance passive layer grows on the chalcopyrite surface without cupric and/or ferrous ions, and that coexistence of these ions causes a formation of another product layer and inhibits the passive layer growth at low potentials. These results are explained by a reaction model assuming the formation of intermediate Cu2S due to chalcopyrite reduction and the subsequent oxidation of the Cu2S. The critical potential corresponds to the redox potential of the Cu2S formation and the predicted values matched with the experimental results. Catalytic effect of silver ions on chalcopyrite leaching was also discussed based on experimental results and the above model.

Jan 1, 2003

By D. Z. Wei

Amine collectors with different structures and length of carbon-chain have been widely used in oxide minerals flotation. In this paper, we synthesized one kind of binary amine, N-dodecylethyl- enediamine, and studied its flotation performance. From the results, we can see N-dodecylethylenediamine which has excellent frothability, is a new type of chelating surfactants. And it also has fine catchability to quartz and hematite. The recoveries of quartz and hematite increase with the augment of N-dodecylethylenediamine concentration. When the dosage of collector reaches 100g/t, the recoveries of quartz and hematite achieve 95.30% and 87.89% respectively. Meanwhile, the influence of pH on the flotation recovery of hematite is studied and test results showed that, as pH increases, the flotation recovery rises until pH=9. And the recovery reaches its maximum in alkalescence. The collector has better flotation capability to quartz than to hematite. And the maximum recovery of quartz is gained in alkaline media, which reaches 97.87%. Finally, the flotation mechanism of N-dodecylethylenediamine is discussed through the measurement of infrared spectroscopy.

Jan 1, 2014

By Francesco Vegliò, Luigi Toro, Francesca Beolchini, Francesca Pagnanelli, Stefano Ubaldini

"Biosorption is an innovative technology used to remove heavy metals from aqueous solutions from mining waters and other industrial wastes. A wider application of this alternative process is strictly dependent on the understanding of the chemico-physical aspects involved, in order to optimize the operating conditions. Mechanistic models are the most useful tools used for understanding purposes, even if the empirical models are still widely applied for their simplicity.In this paper especially propagated biomasses of Sphaerotilus natans, calcium alginate and some waste materials were tested as adsorbents for single and binary solutions containing heavy metals at different pH. The equilibrium experimental results were fitted according to empirical and physical models with growing complexity outlining the inadequacy of the predictive models; in fact, the non-ideal interactions among metals require the insertion of additional correction parameters."

Jan 1, 2003

By K. A. Natarajan

"Interaction with microorganisms results in significant surface chemical changes on minerals. For example, chemolithotrophs such as Thiobacillus ferrooxidans and Thiobacillus thiooxidans significantly alter the surface chemistry of several sulfide minerals such as pyrite, chalcopyrite, sphalerite and galena. Heterotrophic bacteria such as Bacillus sp. could alter the electrokinetic properties of oxide minerals such as hematite, alumina, silica, kaolinite and calcite. Microbe-mineral interactions could thus be beneficially utilised in mineral beneficiation as different from bioleaching. Microbially induced mineral beneficiation unlike bioleaching deals with interfacial phenomena at mineral-solution-bacteria interfaces and surface chemical changes are brought about at very rapid rates amounting to a few minutes resulting in mineral separations in an aqueous medium.In this paper, the role of acidophilic chemolithotrophs such as Thiobacillus thiooxidans and neutrophilic heterotrophs such as Bacillus polymyxa in the beneficiation of sulfide and oxide minerals is illustrated. Mechanisms of bacterial attachment on various sulfide and oxide minerals are outlined with respect to the influence of bacterial interaction in bringing about mineral surface hydrophobicity or hydrophilicity. The role of bacterial cells as well as metabolic products such as bioproteins and exopolysaccharides in significantly altering the surface chemistry of sulfide minerals such as sphalerite and galena and oxides such as hematite, alumina, silica and calcite is discussed with probable mechanisms. Possibilities of generating mineralspecific bioreagents are outlined with respect to bacterial adaptation to mineral substrates."

Jan 1, 2003

By A. N. Zagorodnyaya, Ye. G. Bochevskaya, E. A. Sargelova, Z. S. Abisheva, A. S. Sharipova

"In Kazakhstan, there is a unique sulphide copper deposit, in the ores containing the natural isotope of osmium-187 (more than 90 %). In the pyrometallurgical processing of concentrates for the target metal, osmium is mainly sublimated, with wet cleaning of metallurgical gases (dust and gas mixture) 40 % of it together with rhenium passes into washing solutions (wash acid). On the basis of this acid, the production of ammonium perrhenate was organized at the enterprise of the RSE ""Zhezkazganredmet"" and for the first time in the world practice - the isotope of osmium-187. However, the degree of its recovery from solutions does not exceed 8 % of the amount supplied with the charge or 25 % of the amount that was received for extraction. But the bulk of it (~ 75 %) remains in the raffinate, discharged to sewage treatment plants (wastewater). The studies presented in this work are aimed at solving the problem of osmium isotope-187 extracting from wastewater, which are a potential source of increasing metal production in Kazakhstan. The aim of this work is the development and scientific justification of osmium deposition regimes from wastewater using such reagents as thiosulfate and sodium sulphide. The influence of various physicochemical factors on the precipitation of the osmium was studied and optimal conditions for its maximum transition to sediment were chosen. An original method for obtaining osmium concentrate in the presence of sodium thiosulfate with the addition of potassium iodide from a new type of wastewater - man-made ammonia solutions has been developed. These solutions were combined mother liquors of solid-phase stripping operations and dissolution of pulp of crude ammonium perrhenate. On the basis of the obtained results, a settling technology for extraction of the osmium from man-made ammonia rhenium-containing solutions was introduced at RSE ""Zhezkazganredmet"". It should be noted that the degree of extraction of osmium, depending on its concentration in solutions entering on the settlement, and taking into account the addition of sulfuric acid, will vary from 60 to 90 %. The recovery of osmium during the test period was 58 %."

Jan 1, 2018

By Gábor Mucsi, Barnabás Csoke, Viktor Mádai, Zoltán Molnár, Viktor Török, Ádám Rácz

The application of the stirred media mill in dry mode came to the front only in recent years, but at the same time several questions arise, such as aggregation, agglomeration, sticking on the liners and the grinding media. During high energy milling, not only the particle size reduces, but among others, in numerous cases the crystal structure and the amorphous state of the material also change due to the mechanical activation taking place. The present paper deals with experiments carried out on the ultrafine fly ash grinding in dry mode at various grinding conditions in a stirred media mill to investigate the mechanochemical effect and the energy efficiency of the mill. During the experiments the particle size distribution, particle shape, specific surface area, amorphity and crystal structure of the products were examined. The product related stress model was used for the evaluation of the effect of milling parameters on the mechanical activation. It was found, based on the experimental results, that there is mechanochemical effect on crystal structure of fly ash in the stirred media mill, as it was revealed by X-ray diffraction and FTIR measurements. The experimental results made it possible to determine the effect of the rotor circumferential speed and so the stress intensity on the mechanical activation of fly ash could be revealed.

Jan 1, 2014

By Y. Q. He

The methodology of active pulsing air separation is a new method for dry material classification. Especially, it is suitable to electronic scraps disposal and re-utilization. By studying the difference of drag coefficients of the particles moving through areas of varying Reynolds numbers, and considering the extra-mass forces acting on the particles in the active pulsing air field, models of the dynamic motion which particles follow were developed. A computer simulation was prepared that showed the traces of particles with different densities and/or diameters, but similar aerodynamic characteristics, as they moved through the turbulent flow, to modify and define the parameters of the models. The simulation was found to predict the observed results with artificial tracing spheres being separated by the laboratory equipment. The separation performance, as being affected by the particles, nature, the air velocity, the pulsing frequency and the air pattern, is discussed. In general, lower density particles are more responsive to variations in airflow velocity. In addition, an industrial scale active pulsing air separator was designed, and it provides a new and efficient method for resource re-utilization in China.

Jan 1, 2014

By S. Kelebek, M. Davidson

"Flotation tests were conducted on a mixed copper ore sample containing bornite and malachite with trace quantity of other secondary copper minerals. The bornite component was very floatable, in sharp contrast to poor flotation characteristics of other copper minerals. A Box-Behnken experimental design methodology was used to study effects of three main reagents, namely potassium amyl xanthate (PAX), hydroxamate (Cytec 6494) and diethylenetriamine (DETA). Pine oil, as a frother, was used at a fixed concentration. Three main models constructed using a statistical software included malachite recovery, overall copper recovery, and copper grade. Bornite recovery was not modelled as its recovery was consistently over 99 % in the presence of hydroxamate and PAX. In each model, the hydroxamate dosage was the dominant parameter (at 95% significance level) determining the recovery of main components including that of gangue, which manifested itself by lowering the copper grade of the concentrate. In comparison, PAX was effective only at 90% significance level. DETA did not affect the overall recovery of copper or malachite significantly, but appeared to cause a significant decline in the concentrate grade, especially when used simultaneously with hydroxamate. Various quadratic models developed for the flotation system investigated are presented."

Jan 1, 2014

By Brian Hart, Liuyin Xia, Staman Dimov

The recovery of rare earth elements (REE) is fast becoming of significant interest globally. Modern research and development programs (outside China) towards the optimization of REE mineral recovery by flotation have been lacking. Due to the mineralogical nature of many hosting deposits, the separation and recovery flotation flowsheets can be very complex. As part of a research project, a selected suite of hydroxamic acid collectors (Naphthoyl, Cyclohexyl, Benzoyl, Octyl, Terta-butyl benzoyl, Salicylic) were tested in order to examine their potential for recovery and selectivity. Micro flotation tests were conducted on a feed sample, recovery and grade of the products were used to evaluate their relative flotation efficiency and selectivity and these results (flotation with the hydroxamate collectors) were compared to a phosphoric acid/sulphonate collector mix(shorten as "mixed"). In the testing, the flotation response with the hydroxamate collectors was significantly better than the "mixed" collectors on freshly ground (no slimes removed) samples. Furthermore the tests revealed that for most of the hydroxamate reagents tested, their dosage requirements to achieve recoveries at the same levels was less than that for the "mixed" reagents. Product assays show that recovery of both La and Ce is significantly better for using the salicylic hydroxamate and that Nb, Y and Zr recovery are favored by using octyl hydroxamate. These results indicate mineral flotation selectivity could be achieved by using selective hydroxamtes. Spectral fingerprinting by TOF-SIMS surface analysis has allowed for the identification of reagent species. TOF-SIMS surface analyses of grains analysis confirmed that REE bearing grains reporting to the concentrates are doing so in response to collector attachment whereas grains reporting to the tails are doing so in response to a lack of collector. The TOF-SIMS surface data bas been used to examine the factors promoting flotation stream partitioning.

Jan 1, 2014

By J. Yianatos

The cleaning circuit operation and its effect on the plant metallurgical performance, was characterized at Los Pelambres concentrator, Chile. Experimental data from columns, scavenger and regrinding stages was evaluated. Each stage was characterized by size fractions, and the interaction between stages (columns, scavenger, regrinding) as well as the effect that circulating loads had. The approach for describing the flotation equipment operation (cells and columns) considered the collection and froth zones separately. This methodology allows for the identification of the impact that particle size distribution has on the actual collection and froth transport processes, independently. In this way the effect of regrinding on flotation recovery and grade can be related to the corresponding operating variables, e.g. pulp flowrate, air flowrate, pulp level and pulp density, among others. The effect of gangue entrainment was considered using an empirical dimensionless correlation. The interaction between the circulating load and the overall performance of cleaning circuit was evaluated. The circulating load was defined as the ratio between the solid flowrate of scavenger concentrate over rougher concentrate. It was found that the overall cleaning flotation circuit (column-scavenger) can operate at a relatively high and constant recovery for a wide range of mineral treatment. This is possible when the scavenger has the capacity for compensating the decrease in column recovery at larger circulating loads. Under the condition of high overall cleaning recovery, the rougher stage closely represents the plant recovery. However, at large mineral treatment conditions, the design characteristics (e.g. concentrate transport channel capacity and transfer boxes) as well as instrumentation, control facilities and operation, became bottle-necked. A simulator was developed using empirical models for each stage (column, scavenger and regrinding) in order to evaluate proper operational strategies for cleaning flotation circuits Keywords: flotation, cleaning, regrinding, Vertimill, simulation.

Sep 1, 2012

By E. V. Manlapig

"Some researchers postulate that the floatability of a particle in the streams of an industrial flotation circuit is a function of only its size and liberation properties. They do not discount the importance of reagent or surface contamination on particle floatability but assume that the reagent coverage or surface contamination of the particle surfaces is essentially uniform for particles of similar size and mineralogical properties when subjected to a particular chemical regime.In this paper, samples collected from batch tests performed on different streams of the Red Dog lead cleaning circuit have been characterised with respect to their size, mineral association and mineral surface exposure. An analysis of this data set indicates that particle recovery rate is significantly affected by mineralogical properties - in particular the degree of valuable mineral surface exposure.However, through the use of a nodal analysis technique developed by the authors, it can be concluded that particles with the same size and mineral composition do not all float with the same rate, but with a distribution of rates. The characteristics of this floatability distribution do not change during the flotation process. It is suspected that the particles within a size mineralogical class in this study have varying degrees of surface oxidation and that this results in varying particle flotation rates. Thus basing particle floatability on size and mineralogical effects, alone, in a flotation model is not always valid."

Jan 1, 2003

By Saveliy F. Kaplan, Valeriy N. Tsyplakov, Vasily N. Kovalev, Igor A. Agapov, Nikolai V. Vorob’ev-Desyatovskii

"Based on the experiments, a possibility of successful processing of double-refractory gold sulphide concentrates with a high content of natural organic carbon, which has a high sorption capacity toward gold chloride complexes, has been demonstrated. The proposed approach involves deep burnout of sorption-active organic carbon in an autoclave at a higher temperature and a longer retention time. INTRODUCTION It is known that one of the reasons why gold-bearing ores and concentrates are refractory is the occurrence of fine gold in sulphides (usually in pyrite and arsenopyrite) in ores and concentrates. In addition, refractory gold-bearing ores and concentrates also contain an organic carbonaceous material, which has a sorption capacity towards gold chloride complex, making the ore or concentrate even more refractory. In pressure oxidation, metallic gold is oxidized by Fe (III) aqua-ions and complex Au(Cl)4- ions are formed at temperatures over 180°C, in the presence of chlorides contained in ores. Complex gold anion is adsorbed on the organic carbon surface and then reduced to Au0; the chloride ion is regenerated and gold, adsorbed on organic carbon microparticles, is ultimately transferred to tailings (preg-robbing). Currently, there are several suggestions how to suppress preg-robbing (Simmons, 1998, Pyke, 1999, Rees, van Deventer, 2000, Zhao Jun-wei, 2008). It can be done by reducing the organic carbon content by processing (flotation, etc.),reducing chloride ion concentration by preliminary washing of concentrates in thickeners, reducing the adsorption capacity of organic carbonaceous material by introducing some organic substances that are strongly adsorbed on its surface (blanking agents), and reducing the redox potential of the slurry liquids by introducing neutralizing agents (limestone)."

Jan 1, 2018

By Khoi Nguyen, Keeney. Luke

An outcome of geometallurgical mapping and modeling is the generation of continuous down hole profiles of quantitative geometallurgical attributes at assay scale. These attributes vary from traditional routine data collection methods such as assays and geotechnical logging (e.g. RQD, Fracture Frequency), to new measurements including petrophysical attributes, EQUOtip hardness data and modelled estimates of metallurgical performance indices (e.g. A*b, BMWi). Highly variable continuous geometallurgical data with high spatial resolution can make it difficult to identify spatially continuous domains. An automated method based on the well known time series analysis technique of cumulative summation (CuSum) has been developed which uses statistical analysis to identify domain boundaries in down hole profiles. A bootstrap analysis automatically identifies potential domain boundary locations with associated confidence levels and a series of t-tests determine the significance of defined populations. A hierarchical clustering algorithm is applied to results to enable data sensitivity to be taken into account. The method produces statistically significant populations and is suitable for application on either single or multiple drill hole datasets. Domains defined preserve the inherent variability of the continuous down hole data and provide a method for scaling up variability data (i.e. assay interval scale) to mine scale (i.e. bench scale, block model). A major advantage of the method is its ability to provide suitable input parameters for use in spatial modeling of non-additive and non-linear geometallurgical attributes through conditional simulation techniques.

Jan 1, 2014

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 Chiharu Tokoro

Acid Mine Drainage (AMD), high acid water containing heavy metals discharged from mines, has been recognized as major cause of mine pollution. In Japan, the government spends billions of yen every year to prevent pollution caused by AMD in about 80 abandoned mines. It is widely recognized that the treatment could continue for long decades or an even century. However, costs and environmental loads are uncertain during the treatment because a predictive model for the quality of AMD, the dosage of neutralizer, and the amount of sludge that is applicable for abandoned mines with limited data has not yet been established. In this study, a two-steps predictive model for solution composition and neutralization chemical requirements of AMD in future was constructed based on the geochemical modeling. Requisite input data of the model was the past historical water quality data from AMD monitoring, such as metal concentration and pH in the solution, instead of the sample rocks as other conventional prediction methods. In the first step, solution composition of AMD in the future was extrapolated from the available historical data using geochemical simulation considering the first order kinetics for the mineral dissolution. In the second step, neutralizer dosage and sludge generation in the future was predicted based on the geochemical simulation supposing the chemical equilibrium and oxidation state for all of elements in the solution. Based on case studies of two abandoned mines in Japan, solution composition, neutralizer dosage and sludge generation were estimated. The results of this study demonstrate the effectiveness of our model for the prediction of AMD quality and chemical requirements of neutralization treatment after mine closing. The model is useful for the estimation of the neutralizer dosage and the sludge volume in abandoned mines with limited data. Keywords: acid mine drainage, predictive model, geochemical modeling, first order kinetics, water monitoring

Sep 1, 2012