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By Rodney J. Hundermark, Sharif Jahanshahi, Shouyi Sun

"The major platinum producers in South Africa make use of electric furnaces for the melting of platinum group metal (PGM) bearing nickel – copper concentrates. To gain better understanding of the furnace operation, research was conducted at CSIRO Minerals in Melbourne, Australia. One aspect of the research project was the investigation of the factors affecting the electrical conductivity of melter type slags.Electrical conduction in slags can occur through two mechanisms: ionic and electronic. There is good understanding of the ionic mechanism. In slags containing high levels of iron, the dominant mechanism is electronic as a result of charge hopping (electrons or holes) between ferric and ferrous ions. There is limited understanding of the electronic mechanism and one of the aims of the research was to investigate this mechanism further.Experimental work was carried out at 1450 °C on Al2O3–CaO–FeOx–MgO–SiO2 slags similar in composition to the melter slags (typical composition range (wt%): Al2O3: 5, CaO: 5-15, FeOx: 10-30, MgO: 15-25, SiO2: 40-60). The approach was to vary the oxidation state of three different basicity slags and measure the conductivity response. The slags had molar (CaO+MgO)/(Al2O3+SiO2) ratios of 0.43, 0.64 and 0.94 and FeOx contents of up to 40wt%. A twoelectrode technique was employed with a shallow layer of slag contained in a magnesia crucible. The small amount of slag facilitated relatively quick equilibration (up to one hour) with the gas atmosphere. Experiments were typically started in air and sequentially reduced using different ratios of CO and CO2 gases.Conductivity increased with increasing basicity and increased significantly with iron oxide content. Above 20wt% FeOx, electronic conduction was significant and the conductivity varied with the oxidation state of the slag. The typical response of the conductivity to the change in oxidation state was the following: starting in air, as the slags became more reduced, the electrical conductivity increased to a maximum at around pO2 = 10-7 to 10-4 atm and then decreased with further reduction. The value of the pO2 at which the maximum occurred was dependent on the total iron oxide content and basicity of the slag. The magnitude of the conductivity of the slags increased with increasing FeOx content in a range of 20 to 170 S/m for 20 to 40wt% FeOx. For a given FeOx content in the slags, the oxidation state dependence of the conductivity varied with slag basicity. The trend observed was that the maximum in the conductivity occurred at higher oxygen partial pressures for the lower basicity slags."

Jan 1, 2003

By H. Pearce, A. E. Lewis, A. Ochieng

"Hydrodynamics and mixing are fundamental to the operation of mineral process systems such as flotation cells and metal precipitation reactors. Hydrodynamic conditions influence phase mixing and mass transfer in a multiphase system, and these affect the overall performance of such a system. Detailed information on the effects of the hydrodynamics on the performance of agitated systems is still required for the design and optimal operation of hydrometallurgical systems, which are always multiphase. Computational fluid dynamics (CFD) techniques have been employed to study the hydrodynamics and mixing, most of which have focussed on the performance of axial and radial pumping impellers in agitated tanks. However, very little has been reported on the influence of a draft tube on the flow profile in such systems.CFD simulation of a stirred vessel centres on the way the impeller is modelled. Some of the most recent approaches to modelling an impeller are impeller boundary condition (IBC), snap shot, sliding grid (SG), multiple frame of reference (MFR) and inner outer (IO). The accuracy, with which these models predict experimental results and the corresponding computational demands, form the basis upon which the choice of an approach is made. Most of these approaches (IO, SG and MFR) address the key problem of the stirred tank modelling, namely, the simultaneous meshing of the rotating impellers and the stationary baffles. The MFR is computationally cheap and has been found to give predictions that compare well with experimental data.The CFD technique (code CFX4.4) has been employed in the present work to study the hydrodynamics in a mixing vessel stirred with either a Rushton turbine or a pitched blade impeller. The multiple frame of reference (MFR) approach has been used to model both impellers. A draft tube was used only in the Rushton turbine stirred vessel. The flow profiles for the impellers have been studied in three regions; below the impeller tip, at the middle of the tank, and near the liquid surface. The simulation results were compared with literature data obtained using a laser Doppler velocimetry in the three regions of the vessel, and it was found that the model predictions were better in the impeller region. There was a poor prediction of the experimental results in the region closer to the liquid surface; however, this was improved when the turbulence parameter (C2) in the k-e model was set to a higher value. The value of the impeller clearance at which the Rushton turbine generates an axial impeller type flow has been determined and it has been shown that, at this clearance, a draft tube can be used to enhance axial flow in a Rushton turbine stirred reactor."

Jan 1, 2003

By Å Sandström

Loussavaara-KiirunavaaraAB?s (LKAB) iron ore mine, Kiirunavaara, is of magnetite type and associated with apatite, a calcium phosphate mineral. Rare earth elements (REE) have been found in connection with the apatite but also in other minerals. An apatite concentrate was produced by flotation, in order to investigate the possibilities to extract REE from the apatite by hydrometallurgical means. The content of rare earth elements calculated as oxides (REO) was 0.44% in the concentrate. Initially, leaching was done with large excess of sulfuric acid, hydrochloric acid, and nitric acid to study the REE solubility with different acids. In sulfuric acid, the leaching recoveries of the different REE varied between 35% and 69%. The reasons for the relative low recoveries, were that the rare earth elements precipitated together with huge amounts of gypsum, that was formed during leaching. However, both hydrochloric- and nitric acid gave almost complete extraction of the REE into solution. Analysis of the small leaching residue obtained, revealed, that mainly the light REE remained in the residue indicating that a small part of the light REE were present in the concentrate, in some acid, insoluble mineral other than apatite. With the aim to separate the REE from the phosphoric acid, the solutions from hydrochloric- and nitric acid leaching were neutralized to a pH of approximately 2 with ammonia. During neutralization, REE were precipitated as phosphates with good recoveries and a concentrate of 10.5% REO suitable for further upgrading was obtained, while the remaining solution can be used for fertilizer production. In further solvent extraction studies, it was shown, that after re-dissolution the REE could be effectively extracted by Cyanex 923, thus allowing for purification from calcium and phosphate ions. The REE were finally stripped from the organic phase and a REE nitrate solution was produced. Keywords: apatite, rare earth elements, REE, leaching, solvent extraction, cyanex 923

Sep 1, 2012

Coal preparation plants usually operate with water in a closed circuit mode. In this practice, large quantities of water is continuously being recycled. To compensate the natural losses, only small quantity of fresh make up water is added into the circuit. As a result, a gradual build up of residual concentrations of flotation reagents (frothers, collectors, coagulates etc.) take place in the water and the concentration levels of the contaminants increase. Besides, the recycled water accumulates higher amounts of total dissolved components (1600 ppm) and hardness (740 ppm) than the fresh water. Nearly 80 ? 85% of the process water used in a coal preparation plant is utilized in treating the coal fines in flotation circuit. The presence of certain alkali earth metal ions (e.g., Ca++, Mg++) may adversely affect the flotation performance as they precipitate sparingly soluble hydroxyl complexes on the coal surface and change its surface charge. These studies showed that the use of recycled water in flotation has a significant effect on the selectivity and kinetics of the flotation process because, the dissolved compounds, both inorganic and organic, alter the chemistry radically. By treating the recycled water through a softening process, the concentrations of alkali earth metals and hardness were reduced significantly. The concentration of alkali earth metals and hardness were reduced to 10 ppm and 35 ppm respectively in the softened recycle water. From the selectivity studies, it has been observed that the flotation yield and recoveries increased by four to seven units by softening the recycled water. The kinetic studies indicated that the clean coal particles followed first-order kinetics. The kinetic parameters namely, flotation rate constant (k) and maximum recoveries (R8) of flotation, were found higher with softened recycle water than the recycled water. This reduces the residence time in the flotation cell and thereby, increases its productivity. Keywords: coal flotation, hardness of water, water chemistry, softening process, selectivity, kinetics, flotation rate constant and maximum recovery

Sep 1, 2012

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 F. Karakas

Organo-bentonite production enjoys important applications including solvent based paints and, more importantly, the production of polymer/bentonite nanocomposites. Quarternary ammonium salts in this regard are still considered as the most versatile reagents in the process of hydrophobization. In this study, a purified form of Resadiye region bentonites, which is one of the most significant sodium bentonite deposits in the world, was used. The raw Na-Bentonite was typically characterized by chemical analysis, XRD and DTA analysis and more importantly for its cation exchange capacity (CEC). Other technological properties such as swelling index, pH, apparent viscosity, water absorption, oil absorption were also conducted on the raw bentonite. The mineralogical analysis of the raw bentonite reveals that it contains about 80 % montmorillonite together with other associated gangue minerals including feldspar, quartz, calcite, dolomite, coloured impurities and other clay minerals. The raw bentonite was subjected to two stage processing involving a series of hydrocylones. Different apex and vortex diameters and different pressures were employed in order to produce a bentonite concentrate with 95 meq/100g CEC from a CEC of 71 meq/100 g. This high quality concentrate was used in the production of organo-bentontonite. The modification was performed with two different quaternary amines, i.e. Trimethyl Phenyl Ammonium Chloride (TPAC) and Hexadecyl Trimethyl Ammonium Bromide (HDTMA-Br). In the modification procedure, three parameters, i.e., adsorption density, zeta potential, swelling index and apparent viscosity were studied simultaneous-ly from the same suspension to identify both the mechanism of the process and also the degree of hydrophobicity. Adsorption measurements were made as a function of conditioning period, pH, and reagent concentration. Simultaneous examination of the adsorption density, zeta potential and apparent viscosity enabled us to pinpoint the optimum region of hydrophobicity which was subsequently tested by settling and critical coagulation concentration in both water as polar and toluene as nonpolar solvents. The results are analyzed in the light of experimental data.

Jan 1, 2014

By J. Shibata

The behavior in electric field of fine particles present in aqueous solution was measured in order to apply to the classification of fine particles. The sample particles used are spherical polystyrene particles with the average diameter of 0.03 µm, 0.1 µm, 1.0 µm, 4.3 µm and 9.6 µm. Electrophoretic mobility and zeta potential of various particles are measured by an instrument based on the principle of the laser Doppler effect. The influence of temperature, electrolyte concentration on the electro-phoretic mobility was investigated for various polystyrene particles. The electrophoretic mobility increases with increasing pH and temperature of suspensions. The measured electrophoretic mobilities are different from electrolyte concentration and particle size. The electrophoretic retardation effect and relaxation effect are considered to explain the behavior of fine particles in electric field by applying the electro kinetic theory of Wiersema et al. For all particle size, the electrophoretic mobility decreases rapidly in high concentration of KNO3 such as 0.1 mol/dm3due to the compression of electric double layer The forces acting the particles in electric field are considered to be electrical force, friction force and some other forces like relaxation effect and electrophoretic retardation effect which appear in ionic behavior. It is considered that the particle moving velocity depends on the particle size. When the particle size is less than 1µm, the velocity increases with increasing the particle size. On the oth-er hand, the velocity deceases with increasing in particle size, when the particle size is larger than 1µm. This phenomenon is considered to be interesting from the viewpoint of classification for fine particles. We found that the electrophoretic mobility of 1.0µm particles is larger than that of 0.1µm particles, and that it is possible to classify fine particles by using the difference of electrophoretic mobility by many experimental results. The phenomena can be explained by the forces acting the fine particles in the electric field. We can apply the behavior to classification of fine particles.

Jan 1, 2014

By N. S. Voiloshnikova

Large-scale continuous ?Resin-In-Pulp? process tests were conducted at Irgiredmet. The object for testing was the sample of oxidized gold ore from one of Siberian deposit. Weak-base ion ex-change resin PuroGold was used as adsorbent. The duration of ?Resin-In-Pulp? tests was sufficient for a completing of three cycles ?Adsorption/Elution?. Gold in feed was 0.95 mg/L. Gold in solid phase of adsorption tails? 0.065 g/t. Gold in liquid phase of adsorption tails? 0.026 mg/L. Total gold in adsorption tails ?0.11 g/t. Gold recovery ?94.3 %. The use of regenerated resin had practically no effect on gold losses with adsorption tails. Alkaline cyanide solution (NaCN-20g/L, NaOH- 5g/L) was used as eluent for gold elution from loaded resin. Elution temperature ?60 °C. Number of eluent bed volumes passed ?10. Loaded resin analysis was following (g/ton): Au? 1700~1250; Ag? 400~460; Cu? 250~450; Zn? 5100~9600; Fe? 860~1200. Elution efficiency: Au? 95.3%~97.8%; Ag? 84.0%~88.0%; Cu? 84.0%~88.0%; Zn? 97.0%~99.0%. Although high zinc resin loading was shown zinc was eluted efficiently. The adsorption properties of fresh PuroGold resin, PuroGold resin after 3 cycle ?Adsorp-tion-Elution?cycles in comparison with AM-2B resin were tested. It was shown from adsorption isotherms that selectivity of PuroGold resin slightly less in comparison with AM-2B resin mainly due to its higher zinc adsorption properties. It was founded on base of test results that adsorption properties of PuroGold resin was practically constant during three ?Adsorption/Elution? cycles. Gold may be efficiently recovered by resin tested. There were no difficulties during gold elution from loaded resin and its regeneration. PuroGold resin was recommended for industrial use in RIP process. Process design criteria were developed and plant design is on progress at the moment.

Jan 1, 2014

By Sergey Romanenko, Tatyana Aleksandrova, Karen Arustamian

"Current status of question about grinding stage effect to electrochemistry parameters of operation preparation slurry before intermediate selective flotation was assessed in the present scientific work. Needs of more detail study chemical reactions in the slurry preparation and flotation processes were shown. The ores are polymetallic sulphide type and the one are most difficult for mineral processing. The methodology allows increase information base during floatation tests. Ionometric methods and elements of neural network have been used in the study of mineral processing questions.We have also identified the relationship between the received values of the electrochemical parameters and the technological results in selective flotation. The optimal values of the electrochemistry parameters in operation of the preparation slurry before selective flotation has been found. The main effect of using the proposed methodology is to obtain scientifically based solutions to improve the technology parameters of flotation polymetallic sulfide ores. Challenging issue of selectivity of sulphide-polymetallic ores will be considered using case study of sulphidepolymetallic ores. It was shown that several factors are formed in ore grinding: formation of hydroxyl oxides of iron compounds, copper cation leaching, metal-sulphide and metal-sulphite complexes formation. The chemistry was revealed for current processes in slurry preparation operation before selective flotation. Quantitative assessment of interrelations between electrochemical parameters of slurry and process performance was given with using electrochemical control methods. Neuron network-based model was estimated based on data array and was allowed to establish optimum electrochemical conditions of metal-sulphite complex formation to provide maximum efficiency of selective flotation.INTRODUCTIONPhysical and chemical processes that take place in ore grinding have a significant impact on flotation selectivity and can cause low selectivity of the flotation process. Today this issue is given much attention. In the paper [1] it is pointed out that sulphide oxidation products and slurry components, such as sulphide ions, metallic iron and its oxidation products, have effect on flotation performance. So, metallic iron has impact on metal-sulphite complex formation as a result of oxidation-reduction reactions as follows:"

Jan 1, 2018

By Jacek Kolacz

"Comex has carried out an extensive research work related to optimising sensor based sorting systems. The main target was to achieve efficient separation and maintain high capacity of the process. Eventually, the operating cost of the sorting process was investigated in terms of potential industrial applications and possible replacement of the existing traditional processing equipment. The study included an influence of the following factors on the separation efficiency: capacity, particle size and distribution, particle shape, material properties like colour, density and composition, as well as percentage of the rejected fraction. The above factors were also considered in the calculation models for the operating cost of the sorting process. In addition, other elements were considered like compressed air cost, cost of energy, labour cost, and necessary service and maintenance cost. All these elements were implemented into the calculation model allowing quick and effective evaluation of the major parameters for sorting applications. Finally, the study was carried out for two popular sorting principles: visible light sorting utilising differences in color, texture and shape and X-ray sorting using differences in density and chemical composition. GENERAL INFORMATION ABOUT SORTING POSSIBILITIES Application of the sensor based sorting systems, without any doubt, brings a lot of possible advantages in many mineral operations. The main advantage of the new system is related to its universality and at the same time very sophisticated image processing functions, which can be carried out in the same processing unit (Kolacz, 2014). Figure 1 shows the CXR-1000 system from Comex with 1 m belt width, in the configuration where many different analysed parameters can be used to provide particle separation. The image analysis system includes a camera installed either over the transport belt conveyor or at its discharge end. The system includes the X-ray attenuation analysis realized by the XRT system in the central part of the conveyor belt. The sorting system can be used with both optical and XRT analysis or separately depending on an application."

Jan 1, 2018

By Ersin Yazici, Ahmet Bas, Haci Deveci

Pregnant leach solutions from waste of printed circuit boards (WPCB) leaching contain many impurity metals (Fe in particular) at significant levels. These impurities should be reduced to acceptable levels to avoid problems in downstream recovery processes e.g., low current efficiencies in electro-winning of copper from sulfate solutions in the presence of ferric. In this study, removal of iron in the form of goethite from synthetic (30 g/L Cu2+ and 1 M SO42-) and real leach solutions of WPCB was studied in some detail. The influences of initial concentration of iron (1-4.5 g/L Fe3+), pH (2.5-4.0), temperature (80-90°C) and seeding (23.5 g/L) were investigated over a period of 4 h. A significant increase in the iron precipitation was observed (i.e., from 68% to 96% over 4 h) with rising the pH from 2.5 to 4.0. The addition of seeds had also increased the removal rate over 4 h albeit to a limited extent i.e., from 96% to 99%. For the real leach solutions of sulfate (H2SO4-H2O2) and sulfate/chloride leaching (H2SO4-CuSO4-NaCl), precipitation of iron was found to be 63-73% (pH 2.5) and 93-98% (pH 4.0), respectively. The precipitates were further characterised by SEM-EDS analysis which showed the presence of copper (1-25%) in the precipitates indicating significant copper co-precipitation from the solution. These copper losses can be attributed to the formation of copper compounds such as anthlerite and brochantite within the range of pH (2.5-4.0) tested. This study showed that iron can be readily removed from synthetic/real leach solutions of WPCBs to a large extent (=93%) at the expense of high copper losses particularly at pH 4.0.

Jan 1, 2014

By S. Makni

Flotation is a complex process in which many mechanisms come into interaction. In this paper, an approach to model these mechanisms in order to predict size-by-size flotation performances is presented. The estimation of the collection efficiency of particles takes into account the serial sub-processes of particle-bubble collision, attachment and detachment. The model was applied to an industrial plant and yielded satisfactory results whereby the actual flotation performances could be correctly predicted. Furthermore, the flotation model allowed investigating the possibility of improving flotation performances by a split flotation feed in comparison to the actual single-stage process.

Sep 1, 2012

By Gus Van Weert, Samuel A. Bolorunduro, David B. Dreisinger

"INTRODUCTIONAcid pressure oxidation of high-grade natural acanthite was investigated in the range of 110-150°C and in the sulphate media. High acidity and low pulp density were used to prevent the precipitation of silver.RESULTS AND DISCUSSIONTwo sets of acanthite specimens were obtained from La Valenciana and Ingleterra mines, Mexico. Pressure oxidation tests were conducted on 1 litre scale in a standard 2-litre Parr titanium autoclave.EFFECT OF TEMPERATURE ON THE REACTION OF ACANTHITEThe effect of temperature on the rate of oxidation is presented in Figure 1. The rate of reaction increased with increasing temperature."

Jan 1, 2003

By Ghislain Bournival, Seher Ata, Graeme J. Jameson

A common method to prevent bubbles from coalescing in a flotation cell is by the addition of surfactants, called frothers. The gas dispersion properties in a column were tested for solutions of 1-pentanol, tri(propylene glycol) methyl ether, and poly(propylene glycol) in the presence of sodium chloride. The dependency of surfactant on the gas holdup can be divided into regions. It seemed that for a sufficiently low concentration of surfactant, even a stronger surfactant could show a transition in gas holdup from constant/decreasing to increasing with concentration. This region, however, was not marked by a decrease in the average bubble size. In addition, PPG gave higher gas holdup values while averaging larger bubbles. On the other hand, sodium chloride mostly affected the gas holdup when the concentration was high enough to prevent bubble coalescence. Another parameter affecting the gas holdup was the superficial gas velocity. A linear dependency was found between the two under a bubbly flow regime. The current study showed that both surfactants and salt could slightly affect the influence of the superficial gas velocity on the gas holdup.

Jan 1, 2014

By Douglas W. Fuerstenau

Some historical sketches of the early development of froth flotation are presented. Flotation technology involves several aspects: chemical control of mineral hydrophobicity, selectivity in flotation, flotation kinetics, flotation machines, and process optimization and control. However, only some aspects of the regulation of mineral flotability by the addition of chemical collectors in some selected cases are discussed. The early contributions to flotation science by Langmuir, Gaudin, Wark, and Taggart are briefly outlined. With a firmer understanding of surface chemistry, electrochemistry, and the electrical double layer, progress has been made in understanding the fundamentals of flotation chemistry, although sound theoretical underpinnings still are needed in these very complex systems. Flotation chemistry is related very directly to the type of mineral being floated since the systems depend strongly on the chemical and physical characteristics of the minerals. Full discussion of chemical reagent phenomena would be in terms of the behavior of naturally flotable minerals, sulfides, oxides, silicates and alumino-silicates, and salt-type minerals. At this time, citing a few cases involving salt-type minerals and oxides, the dependence of their flotation surface chemistry will be discussed in terms of the role of adsorption, surface reaction, and the hydrophobic effect.

Sep 1, 2012

By N. Panteleeva, E. Konoplev, I. Michailova, S. Titkov, T. Gurkova, T. Chumakova, Sylvinit Co.

"INTRODUCTIONFlotation of mineral particles by cationic surfactants – namely alkyl amines and their derivatives – is finding ever growing application in processing of various ores and in quality refinement of the benefication end products, iron concentrates for example. In the recent years application of cationic collectors - alkylmorpholines - enabled the development of new highly efficient procedure of water-soluble mineral processing, being also the one with low energy consumption. This procedure is a reverse flotation of carnallite from bay salts of salt-pans and from carnallite ores.The efficiency of cationic SAS influence depends upon colloid-chemical state of the collector in flotation liquid phase, especially if the latter comprises mineral salts. Availability of clayey impurities or slime particles of iron oxide in cation flotation feed, which actively sorb the cationic collector, deteriorate considerably the cation flotation performances. In Halurgy Institute the investigations of cation flotation under potash and carnallite ore processing have been carried out, and new reagent modes, enhancing cationic surfactants sorption at mineral particles, have been developed. Application of new reagents enables one to decrease considerably the consumption of expensive cationic collectors and to enhance the floatability of coarse mineral particles."

Jan 1, 2003

By E. Ashirbaeva

"Ores of ferrous metals traditionally make up the bulk of recoverable reserves of solid minerals, and iron ore concentrates - in the processing and consumption. To obtain concentrates, three main methods are used: dry and wet magnetic separation, gravity and flotation. But even their integration into complex developed schemes with finishing operations often do not solve the problem of obtaining high-quality concentrates, which are necessary for powder metallurgy and electric steelmaking. Increasing the iron content in the concentrate by removing harmful impurities is the goal of this work. The possibility of reducing the operations of wet magnetic separation twice and completely eliminating concentrating operations in ball mills from the scheme of operations has been established. Selective leaching agents for each type of iron ores have been created, allowing to obtain concentrates with an iron content of not less than 68-69% and negligible concentrations of harmful impurities. Methodical recommendations for long-term storage of bioreagents in the active state, their immobilization and preparation in industrial conditions at the enterprise Nedropolzovatelja are developed. The proposed biotechnology, which allows to obtain high quality iron and conditional concentrates for harmful impurities, is protected by patents (RU 2537684 ""Method for fine-tuning of high-sulfur magnetite concentrate"" for magnetite ores and Pat. RU 2599068. For the industrial implementation of the new technology, organizational and technological measures have been developed in the system with Road maps for types of ores. The developed technology makes it possible to condition noble metal, tin, tungsten, nickel and other concentrates in harmful impurities such as arsenic, antimony, mercury, sulfur, copper, zinc, iron, phosphorus, manganese, in total 30 components that pass into solution under the influence of bioreagents.INTRODUCTION Consumption of various metals is steadily increasing every year, the volume of mining is constantly increasing. Ores of ferrous metals traditionally make up the bulk of the recoverable reserves of solid minerals. Enrichment technologies for iron-containing ores are reduced to the combination of three main methods: wet and dry magnetic separation, gravity and flotation. But even the use of complex advanced technological schemes often does not lead to the production of high-quality concentrates suitable for metallurgical processing. In this case, either lapping operations or effective technical and technological solutions are used in the main enrichment cycle. Widely used in practice methods for improving the quality of iron ore concentrates include the use of finishing operations (fine screening, reverse cation flotation), staging of concentrates, the use of more sophisticated equipment (separators with running magnetic field, magnetic gravity classifiers, column flotation machines)."

Jan 1, 2018

By E. Emelyanenko, P. Solozhenkin, J. Yagudina, O. Ibragimova

"To recover tetrahedrite-tennantite series minerals from porphyry copper-pyrite ores by the froth flotation method, further research on thiol collectors is launched to promote the utilization efficiency of copper ores. In the present paper the adsorption mechanism of the collectors on tennantite surface has been investigated by computational modeling and FTIR-spectroscopic analysis, which have revealed that the decrease in prognosis of collector activity evaluation (PCAE) for tennantite is in the following order: BX (-0.34318), AEROPHINE 3418A (- 0.61756), AERO 5100 (-14.18857). The lower PCAE the stronger the ability of the collector to interact with the mineral surface of tennantite and form the stable complex. More kinetic reliable conditions to form suitable adsorption layer and rupture of the liquid interlayer with AERO 5100 have been observed by FTIR spectra due to decrease of the intensity and stretching and bending vibrations of water (less than 20 and 65%, respectively). In order to verify the feasibility of AERO 5100 as a collector the industrial flotation tests have been conducted. Flotation performance has improved significantly with the stadially grinding and preflotation of tennantite in intercycle copper flotation that allows to avoid desliming of the fragile mineral and minimize loss of Cu and As in tailings. The recovery of copper in copper concentrate increases by 3.9% with the grade maintained.INTRODUCTIONCopper is one of the first metals extracted and the main material of choice for different high-technology applications today. Currently 80% of the world's copper comes from copper sulfide ores. However, due to the depletion of high-grade copper ores in the world and constantly growing demand for copper, the need to develop processes and technologies to treat copper resources from additional sources such as mine tailings, low grade deposits, industrial wastes and deposits with high impurity levels such as As and Sb will continue to increase (Miller and Craig, 1983). The beneficiation processes of copper-pyrite ores consisting of tennantite-tetrahedrite series minerals are generally complex. Tetrahedrite-tennantite minerals occur as fine anhedral grains intermixed with grains of galena, sphalerite, chalcopyrite, pyrite and other sulfides (Saharova, 1966). The mineralized zones of Southern Urals, Russia deposits correspond with these ore types but tennantite-tetrahedrite series are more abundant in ores at the Uzelginskoye deposit, some samples of which contain 70% of copper in tennantite form (Seravkin et al., 1994). This deposit differs from other similar copper-pyrite ores by thin mutual ""germinating"" minerals and higher content of arsenic (up to 0.8-1 %) which create additional considerable problems in enrichment (Solozhenkin et al., 2016)."

Jan 1, 2018

By Sonia Helle, Ursula E. D. Kelm

"From a metallurgical point of view, acid leaching of oxide zone copper ore is considered in the first place in terms of ore grade, whole rock mineralogy, rock granulometry, crushed aggregate size distribution, porosity, permeability and corresponding fluid flow characteristics. Despite exhaustive physicochemical and general mineralogical characterization, drops in copper recovery occur and are often attributed to and “unquantified mineralogical misbehaviour” of the gangue phases. This study establishes an experimental link to monitor and quantify the chemical interaction of chrysocolla, malachite and atacamite with reactive gangue phases.Laboratory-scale sulphuric acid (15%) leaching in small columns is carried out using a synthetic rock composed of 57% quartz, 1% ore phase, and 42% reactive gangue. Gangue phases were selected to represent mineralogy found in argillic, advanced argillic, and propylitic alteration zones. Exotic copper ores of Codelco Norte (in particular Mina Sur) served as model for the modal distribution of mineral phases. Natural reactive gangue phases (<200 Tyler mesh) were chosen as pure as possible: Saz-1 and Swy-1 montmorillonites, KGa-1B and KGa-2 kaolinites (all Clay Mineral Society, USA, Source Clays) Nau-2 nontronite, Imt-1 illite (both Clay Mineral Society Special Clays) and Chilean mordenite, laumontite and bentonite. Ore phases are: mineraloid chrysocolla from Radomiro Tomic (Codelco Norte), reagent grade malachite and a purpose synthesized atacamite-paratacamite mixture. Complete chemical, physicochemical and mineralogical characterizations were carried out for ore and gangue phases.The following observations hold for samples with and without mineralization: Smectite-rich gangue increased up to 75% in volume. Once wet, air-filled vesicles formed due to the rapid sealing effect of overlying smectite in the column. No volume change occurred for illite, mordenite and kaolinite gangues. For kaolinite mixtures acid puddles formed on top of the column during initial leaching due to the delamination and barrier formation of this phyllosilicate. Fluid recovery was <60% for expandable phases and reached up to 80% for non-expandable mixtures. These observations confirm the very low extractions obtained in ore with a combined smectite – kaolinite gangue for Mina Sur. The most important mineralogical changes observed in the solid residues are: reduction of basal smectite phase reflections (XRD), and slight loss of illite intensities. This is also reflected in the major element composition of the residues, which demonstrate a loss of Mg, Mn, Ca, Na, K followed by Fe, Al and Si; with their proportions depending on the starting materials. Furthermore, alunogen and meta-alunogen formed, with related phases coquimbite (illite) and godichite (nontronite) also depending on gangue mineral chemistry. For laumontite samples, meta-alunogen and alunogen precipitated from the leachate."

Jan 1, 2003

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