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By M. Minagawa, G. Granata, C. Tokoro, T. Kato

"In this work, we studied the mechanochemical activation of chalcopyrite by vertically stirred ball milling (VSBM) to enhance the dissolution of copper. By using x-ray diffraction (XRD) and laser diffraction particle size analysis, we investigated the effect of milling and milling conditions on particle size and phase composition of the chalcopyrite concentrate. To elucidate the efficiency of VSBM towards the mechanochemical activation of chalcopyrite, we also conducted leaching experiments in sulfuric acid-ferric sulfate media. Under all investigated milling conditions, the VSBM determined a dramatic decrease of particle size from over 100 µm of P80% up to about 13 µm. Furthermore, the XRD of the ground chalcopyrite specimens highlighted a partial oxidation of the mineral. In leaching, upon grinding by VSBM, the increase of copper extraction ranged from a minimum of +10% to a maximum of +40%, depending on the grinding conditions. In order to elucidate whether the dissolution enhancement was a consequence of the decreased particle size or of an induced mechanochemical reaction, we performed leaching experiments on activated and non-activated chalcopyrite sample having the same particle size. In addition, we determined the activation energy of leaching before and after vertically stirred ball milling. The leaching results on samples with the same particle size highlighted a greater copper extraction and higher dissolution rates upon mechanochemical activation. Whether performing grinding by VSBM or not, the leaching kinetics was found to be controlled by the chemical reaction on the surface of the chalcopyrite particle. By grinding the chalcopyrite concentrate by VSBM, the activation energy of leaching slightly decreased from 66 to 58 kJ/mol. INTRODUCTION Due to the increasing demand of copper, low grade ores and refractory minerals like chalcopyrite are expected to become the main copper source in the next years (Klauber, 2008). As a low-grade sulfide, chalcopyrite shall be processed hydrometallurgically. However, due to the formation of a protective layer of elemental sulfur during the oxidizing leaching, the dissolution of copper is slow and/or incomplete (De Bernardi and Carlesi, 2013). Therefore, the development of new technologies to enhance the extraction of copper from chalcopyrite is highly required."

Jan 1, 2018

By L. A. Vaisberg, E. V. Shishkin, S. V. Kazakov

"This research is targeted at finding solution to the problem of reduction of specific energy consumption during disintegration of solid materials with the help of machines, operating in a quasiresonant mode. The objective of the research is the development of an energy-saving method of disintegration of supestrong rock and by-products on the basis of vibrational units with two movable crushing elements, operating in a rigorous synchronous-antiphase mode without stringent kinematic links. In the course of investigations a mathematical analysis of the dynamics of vibrational units was performed to determine required mechanical parameters, allowing for adjustment of the machine actuating elements to high-frequency synchronous-antiphase oscillations in the quasiresonant frequency range. As a result of performed pilot tests, the reliability of desktop studies was confirmed and the dependency of process parameters on the machine regulated parameters in the quasiresonant frequency range was identified. The analysis of obtained data showed that during machine operation with cone-shaped crushing elements in the quasiresonant frequency range, the yield of the high-quality finished product (WFA grits of -3+1 mm grain size class) in one pass reaches 35%, whereas the form of the particles corresponds to the grain form with sharp edge. The quasiresonant operation mode of the vibrational unit with two freely suspended crushing elements (without stringent kinematic links) provided substantial reduction of energy intensity during crushing down to 0.16 kWh/t, which shows reduction of power consumption for crushing by more than 15% compared to conventional equipment.INTRODUCTION The most common and energy-consuming processes in the mining industry are the crushing and grinding of various solid materials. Such large energy costs are due to the fact that the capabilities of the existing crushing and grinding machines are based on traditional methods of destruction, and are limited by their kinematic features, which do not allow to reduce the energy intensity of processes, to lower the irreversible loss of useful components, to improve the quality of marketable products. In connection with the foregoing, the task of energy costs reducing for disintegration is one of the most important issues in the enrichment of both minerals and processing of man-made raw materials. The solution of this problem is possible only through the creation of a fundamentally new highly efficient technique and technology for processing raw materials [1, 2]. It seems that the greatest prospects in this respect are the vibration methods of disintegration, in particular, the vibratory cone crusher based on a two-mass system without rigid kinematic connections between the crushing bodies, with vertical vibrations of the working bodies. In this machine, the principle of rational material destruction is realized – crushing without re-grinding [3-5]."

Jan 1, 2018

By J. Seo, W. Kim, I. Bae

"Microcrystalline silica impurities such as quartz and opal-CT commonly associated in bentonite should be controlled and removed as far as possible when bentonite is used as biocompatible raw material because they show sufficient evidence of carcinogenicity. Since opal-CT contained in bentonite in trace amounts cannot be well separated by conventional sedimentation method, in this work, the ultrasound-assisted removal of the impurity was attempted. Irradiating ultrasound into bentonite-water suspension promoted the production of fine montmorillonite particles in the suspension and the production markedly increased when montmorillonite was activated by Na2CO3. Subsequent centrifugation of the suspension made it possible to recover pure montmorillonite particles as an overflow product. Only 16.2 mass % of total solids was recovered as an overflow from the non-activated suspension, whereas 63.5 mass % was recovered from the activated suspension at centrifuging speed of 10000 rpm. Increasing sonicating time enhanced the yield of overflow, however, excessive sonication up to 10 min hindered the purification of montmorillonite. It was observed that the peak reflection of (101) plane of opal-CT in overflow increased as sonicating time increased during prolonged sonication. INTRODUCTION Bentonite consisting predominantly of mineral montmorillonite is clay-rich soft rock generated frequently from the alteration of volcanic ash. Depending on the nature of its genesis, bentonite contains a variety of accessory minerals, which may include mainly quartz, feldspar, opal cristobalite/tridymite (opal-CT), calcite, illite and mica. The presence of these accessory minerals can impact the industrial value of the deposit, reducing its commercial value depending on its applications. Therefore, bentonite is often purified by removing these impurity minerals for special applications where specific properties and characteristics are required (Murray, 1999). Among the special applications, bentonite is often used in the cosmetic and pharmaceutical industry as both excipient and active ingredient in the forms of liquid (suspensions, emulsions), semi-solid (creams, ointments) and solid (powder, capsules and tablets). The basic requirements for bentonite to be used as raw material are pure, microbiological and mineralogical inertness. Physical properties such as swelling volume and gel formation are also important. Particularly, microcrystalline silica polymorphs such as quartz, cristobalite and opal-CT should be controlled and removed as far as possible because they show sufficient evidence of carcinogenicity in humans."

Jan 1, 2018

By Vladimir Vigdergauz, Elena Belogub, Dmitriy Makarov

The influence of supergene oxidation on physicochemical and technological properties of polysulfide ores was studied. Modeling and analysis of oxidation pyrite copper-zinc ore samples from the Valentorskoye deposit show that sulfide floatability is decreased by the longer-term oxidation. The treatment of oxidized samples by sulfuric acid in oxidative conditions and its impact on the elemental sulfur composition on the surface of sulfides was discussed. It is shown that an enhancement of the floatability of sulfides of oxidized polysulfide ores after leaching by sulfuric acid could be perspective for the developing of combining floatation-hydrometallurgical technology of the nonferrous metals recovery.

Jan 1, 2014

By Arkady Senchenko, Yuri G. Seredkin, Alexander Aksenov

"This paper describes the development of efficient technology for the treatment of complex ores containing gold and copper as major valuable components, where silver is present as well. Copper is mostly represented by oxidized minerals in these ores; however, copper sulfides are also present. Gold is present in its free form and in associations with oxidized and sulfide minerals; silver usually accompanies gold. Complex composition of the ore requires complex solutions for their treatment. The results of searching for the techniques to recover valuable components are described in this paper. Gravity methods allow for free gold recovery, flotation methods allow one to recover major part of copper and precious metals in associations; and in the result of leaching process additional amount of copper, gold and silver is reported to solution. Combining all these methods help achieving high levels of valuable components recovery. When implementing a combined technological flowsheet about 80 % of copper goes to concentrates from gravity and flotation of sulfide and oxidized copper minerals; and sulfuric acid leaching allows increasing total copper recovery up to 90 % and higher. Major part of precious metals (up to 90 % of gold and 80 % of silver) is recovered to these concentrates, and after hydrometallurgical treatment it is possible to increase gold recovery up to 96 %, silver recovery - up to 90 %. The suggested technology helps solving the problem of precious metals recovery from complex gold-copper ores, and allows treatment of the ore with different proportion of sulfide and oxidized minerals, and at different valuable components grade."

Jan 1, 2014

By C. Tokoro

Co-precipitation of dilute toxic anions with ferrihydrite is an important removal mechanism in wastewater treatment system. Although, numerous qualitative studies have been published on removal characteristic from wastewater of dilute anions by co-precipitation treatment, detail mechanism or quantitative characteristic is not well understood. This paper discussed the co-precipitation mechanism of As(V) and Cr(VI) with ferrihydrite by comparative experiments between co-precipitation and simple adsorption. In this study, co-precipitation experiments and simple adsorption ones were distinguished closely. In the former, precipitation of hydroxides and adsorption of anions develop simultaneously, but in the latter, anions adsorb onto prepared hydroxides. Although high affinity anions for hydroxides (e.g. As(V) for ferrihydrite) showed quantitative difference of removal ratio between co-precipitation experiments and simple adsorption ones, low affinity anions (e.g. Cr(VI) for ferrihydrite) showed quantitative agreement in spite of deferent forms of ferrihydrites between them, that is, amorphous ferrihydrite was formed in co-precipitation experiments, but goethite was formed in simple adsorption ones. In order to discuss the mechanism of co-precipitation phenomena, three experimental studies have been carried out: (i) adsorption isotherm measurement in the co-precipitation experiments of As(V) or Cr(VI) with ferrihydrite, (ii) zeta potential measurement of co-precipitated or simple ad-sorbed ferrihydrite with As(V) or Cr(VI), and (iii) XRD analysis of co-precipitated As(V) for ferrihydrite. All experimental results suggested the main mechanism in co-precipitation phenomena of As(V) was not only a surface complexation (simple adsorption) but also a surface precipitation.

Jan 1, 2014

By Xingshi Yang, Ghislain Bournival, Seher Ata

"Particle-laden interfaces are a fundamental research topic in froth flotation since the process involves particle-coated bubbles in both the pulp and the froth phase. In most experimental studies the characteristics of the particle layer in multi-bubble systems are poorly defined. An experimental setup has been developed based on a Langmuir-Blodgett (L-B) trough. The modified trough allowed introducing an air bubble beneath the particle monolayer formed at the air-water interface which made the study of the interaction between the bubble and the monolayer under various pH values possible. The monolayer characteristics of the particles were also studied and compared in terms of surface pressure (?-A) isotherms and packing factor. On compression, the particles formed branched structure at high pH whereas a uniform monolayer was formed at lower pH. Observations related to the behavior of particles during compression and expansion cycles, and the coalescence of a bare bubble with the flat particle laden interface were provided and the implication of the results for flotation process was discussed.INTRODUCTIONFroth flotation is known for its versatility and ability to concentrate low-grade, complex ores. It is considered a physico-chemical process in which particles attach to air bubbles, depending on their hydrophobicity as well as other factors, and are carried to the surface to form a froth layer. Reagents are used to stabilize bubbles and the froth layer (Pugh, 1996). However, particles, which are carried by the bubbles or entrained, significantly contribute to the stability of the froth phase (Ata et al., 2003; Zanin et al., 2009; Bournival et al., 2015a). Their relevance in mineral processing has led to a number of fundamental studies on the effect of particles and their properties on the process of froth flotation.Flotation systems are particularly difficult to characterize due to the broad range of properties of particles (e.g. size, liberation, hydrophobicity, etc.) and inconsistent operational conditions (e.g. changes in water quality, reagent addition, etc.). Several studies have made the use of well characterized particles in laboratory conditions. Such studies allowed the finding of an optimal contact angle for the stabilization of the froth phase (Johansson and Pugh, 1992; Ata et al., 2002). Froths have a large number of bubbles so that individual interactions are not observed. The study of two bubbles allows to determine the stability of the bubbles, with particles, and to some extend the stability of the bubble-particle aggregate (Gourram-Badri et al., 1997; Bournival et al., 2015b). The removing of particles between two bubbles may also be studied from a Scheludko cell (Johansson and Pugh, 1992) or by observing a bubble with a flat interface (Sethumadhavan et al., 2002). However, these systems provide limited information on the arrangement of the particles."

Jan 1, 2018

By S. S. Lu

In sodium oleate and salicylhydroxamic acid systems, sequence of floatability of three sulfate minerals is: barite>celestite>gypsum, in lauryl amine system is: gypsum>celestite>barite. XPS and infrared spectrum analysis are used to find that it is chemical reaction between sodium oleate and three minerals, physical adsorption on the surface of minerals for lauryl amine, and it is chelating reaction between salicylhydroxamic acid and three minerals possibly. Theoretical calculation on chemical bonds in crystal structures of three minerals is carried out, finding that breaking degree of Mn+?O2- in crystal structures of three sulfate minerals is closed related with floatability.

Jan 1, 2014

By V. A. Chanturiya

The application of High-Power Nanosecond Electromagnetic Pulses (HPEMP) irradiation in dressing of resistant gold- containing ores appears attractive as this technique provides for a significant increase in precious metal recovery (30-80% for gold and 20-50% for silver), therewith helping reduce both energy consumption and the cost of products. The prospects for applying pulsed power technologies in the mineral processing in order to increase the contrast between the flotation properties of raw minerals dictate the need to perform special studies of the effect of HPEMP on the structural state, phase composition, and physical and chemical properties of surfaces of sulfide minerals as the main carriers of precious metals. This study deals with plausible mechanisms of the micro- and nanophases formation on the surfaces of sulfide minerals under the effect of high-power nanosecond electromagnetic pulses (HPEMP) with high electric field strength ~107 V/m. This paper discusses reasons for the changing of flotation behavior of natural pyrite and arsenopyrite during the pulsed-power treatment. It was concluded that HPEMP treatment may be regarded as a tool to change the surface composition and sorption ability of collector (xanthate) onto mineral surface, and, therefore, it allows to control the hydrophobic-hydrophilic surface balance. Single mineral flotation tests have been shown the significant increasing of the pyrite recovery while the arsenopyrite was depressed. The results of gold containing pyrite (pyrrhotite)-arsenopyrite ore flotation in batch approve the decreasing of arsenic recovery in sulfide concentrate. Keywords: pyrite, arsenopyrite, high power nanosecond pulses, activation, selective flotation

Sep 1, 2012

By M. Kosugi, M. Kawata, J. V. Satur, K. Mitsuhashi, R. Kawarabuki, W. Kracht, Y. Ebisu

Copper concentration is becoming more difficult because remaining copper ores are more complex and of finer copper mineral grain size, making copper minerals harder to float because of the fine particle size required to liberate the valuable species. The purpose of this work was to study the flotation behavior of fine copper sulfide ores at different conditions of agitation and aeration. The experimental campaign was carried out in a laboratory Denvertype flotation cell of 1 L volume modified to be operated with forced air that allows decoupling air flow rate and agitation speed. Four ore samples from Chile were used, all of them containing copper sulfides such as chalcopyrite, bornite, chalcocite, and tennantite, but with varying grain sizes and compositions. Preliminary flotation tests for establishing the flotation conditions of grinding size and collector dosage were conducted before the kinetic flotation tests that were carried out at different agitation speeds varying from 900 to 1300 rpm for gas flow rate ranging from 1.6 to 7.2 L/min. The flotation products were analyzed by ICP-MS and MLA (Mineral Liberation Analyzer). The results showed that high agitation speeds with corresponding air flow rates resulted in better recovery than moderate agitation speed and air flow rate, and an excess in gas flow rate resulted in bad performances. The flotation rates of the fine copper minerals were improved despite the different improvement rates among the fine size fractions. The impact of these operational variables, however, was different when comparing the results for the four ore samples. While it was found that the order of floatability in the four samples was the same, that is, chalcocite > tennantite > bornite > chalcopyrite, the kinetic constants of the copper minerals in the samples were different, indicating that mineral composition in the sample affects the flotation kinetics.

Jan 1, 2018

By T. Kalliomäki, B. P. Wilson, M. Lundström, J. Aromaa

"The diffusion rate of cupric ions and limiting current density are important factors that determine the rate of copper mass transport in electrolytes proximal to the electrodes used in electrorefining. As a result, diffusion can critically affect both the rate and morphology of cathodic copper deposition thus it is crucial that it be optimized to improve production. The diffusion coefficient of cupric ion (DCu(II)) in copper electrolytes has been previously researched but the values detailed in the literature show significant variations and moreover arsenic - a common impurity - is generally excluded. Furthermore, in previous studies the models have only been validated with model solutions rather than real industrial electrolytes. In this study, the limiting current density and diffusion coefficient of cupric ion were defined for synthetic electrolytes containing copper (40–60 g/dm3), nickel (0–20 g/dm3), sulfuric acid (130–220 g/dm3) and arsenic (0–45 g/dm3). The cathodic limiting current densities were measured at three temperatures (50, 60, 70 °C) with linear sweep voltammetry using the rotating disc electrode (RDE) as the cathode. By utilizing the limiting current density, models for the DCu(II) were constructed using Levich equation. The validity of the DCu(II) model for technical use was confirmed through their application to industrial electrorefining electrolytes with known element concentrations. Consequently, this study provides improved models for limiting current density and diffusion coefficient of cupric ion that can be utilized for industrial process optimization.INTRODUCTION For an efficient copper electrolysis process, the mass transport of copper ions has to be effective. The main mass transport types of copper ions in copper electrorefining are diffusion and convection while the effect of migration is negligible. In order to maintain good mass transport, it is beneficial to keep both diffusion and convection high to maximize the limiting current density (jlim) (Bard and Faulkner, 2001). jlim is the highest current density that can flow in the cell, thus by maximizing jlim the deposition time can be minimized and the good quality of cathodic copper can be ensured. Thus, it is important to research possibilities that increase and optimize diffusion since slow diffusion in the electrolyte limits the rate of the process (Levich, 1947; Moats et al., 2000; Subbaiah and Das, 1989)."

Jan 1, 2018

By T. Suzuki

Acid leach liquors from spent lithium-ion batteries employing lithium cobalt dioxide (LiCoO2) as a cathode active material contain valuable metals such as cobalt and lithium, as well as common metals such as aluminum and copper. The objective of this study was to develop a hydrometallurgical process providing a high selectively between aluminum, cobalt, copper, and lithium from hydrochloric acid solutions. Batch experiment results showed that selective hydroxide precipitation approach was not suitable because a significant amount of cobalt and lithium was co-precipitated with aluminum and copper hydroxides. In contrast, batch experiments and the subsequent data analysis indicated that the sequence of solvent extraction circuits using PC-88A, Acorga M5640, and tri-n-octylamine (TOA) extractants effectively separates four metals of interest. In the first circuit of the proposed process, copper was selectively extracted by Acorga M5640 at the pH 1.0-2.0. Aluminum, cobalt, and lithium remain in the aqueous phase. In the second circuit, aluminium is selectively extracted by PC-88A at pH 2.0-2.5. For the separation of remaining cobalt and lithium, Acorga M5640 provided higher separation efficiency compared to PC-88A single extractant and PC-88A/TOA mixed extractant. However, the stripping efficiency of cobalt from the Acorga M5640 organic phase was found to be low (less than 10 %). Therefore, PC-88A/TOA mixed extractant rather than Acorga M5640 is an advisable choice for the separation of cobalt and lithium. Keywords: spent lithium-ion secondary batteries, solvent extraction, lithium, cobalt

Sep 1, 2012

By M. Paymardi, A. Foroutan, T. P. Oladele, M. Abbaszadeh

"Reducing the amount of zinc and iron in lead concentrate is one of the important aspects of processing in lead and zinc flotation plants which results in improvement of lead concentrate quality and prevents zinc loss. In mineral flotation industries, lignin sulfonates are known for their depressant properties for both non-metallic and sulfide minerals such as pyrite and pyrrhotite.This paper investigates the effect of lignin sulfonate on flotation of galena, sphalerite and pyrite in sulfidic lead and zinc bearing ores. Batch flotation tests were carried out on a high pre-activated zinc samples. The feed contains 0.9% lead, 2.3% zinc and 7.5% iron. The dosage of all reagents such as sodium cyanide, zinc sulfate, ethyl xanthate and methyl isobutyl carbinol (MIBC) were kept constant for lead flotation step except calcium lignin sulfonate (CLS) that was varied between 0 and 80 gr/ton.Results for lead rougher concentrate showed that the grade of lead increased by 2.7% while the recovery decreased around 4 % at the highest dosage of CLS. Furthermore, zinc recovery decreased by 6.3% with no significant change in grade. Iron recovery in lead rougher concentrate decreased by 2.3 % while the grade changed around 1%. In sphalerite flotation step, CLS dosage was changed in the range of 0 to 80 gr/ton while the dosage of other reagents such as copper sulfate, lime, amil xanthate and MIBC were kept constant. In this step, no decreasing in grade and recovery of zinc was observed, while iron recovery decreased. It was suggested that CLS has a depression effect on sphalerite in conjunction with other zinc depressants such as zinc sulfate and sodium cyanide. CLS was further used in plant with non-pre-activated zinc minerals. Similar trends were observed in plant.INTRODUCTIONlead-zinc sulfide minerals play an important role in the production of lead and zinc metals in the mineral processing industry (Luo, Feng et al. 2016). Due to complexity of the lead-zinc ores mineralogy, in some situations, their flotation properties vary significantly from one deposit to another one even in itself (Bulatovic 2007)."

Jan 1, 2018

By Christopher M. Rule, Martyn P. Hay

"A methodology was developed in the mid-1980’s to predict plant performance from standard laboratory flotation tests. The methodology incorporates a flotation simulation program “SUPASIM” which translates flotation performance from bench-scale tests to full-scale plant. The technique is based on a simple, empirical kinetics model, and is tailored for use by the practical metallurgist. Kelsall’s unmodified equation incorporating two rate terms describing slow and fast floating components is used as the basis of the method. The flotation behaviour of an ore is described by a set of numbers, which can be compared in the evaluation of ore types, mineralogy and operating conditions. In so doing a precise relationship is developed between metallurgical performance in terms of grade and recovery and flotation kinetics.To date the performance of more than 20 flotation plants has been predicted, encompassing copper, lead, zinc, nickel, phosphate, pyrite, graphite, cassiterite, platinum and various slags. In three cases, plants have treated more than one type of ore. The method has successfully been used to predict and design four flotation plants using data generated from bench-scale laboratory flotation testwork. All have since been commissioned, and have performed as predicted. In the last year alone it has been used to drive flowsheet development for at least seven new plants in South Africa and the Americas. It is also being used to assist in the optimisation of existing operating plants."

Jan 1, 2003

By Z. G. Li

The large-scale vibrating screen has been applied widely in coal industry and other industrial areas as a kind of important device. As vibration mechanical device, it works very hardly and works in very bad environment so that the structure of screen is damaged easily. Therefore, it is very important that how to detect the fault of structure as early as possible to make the repair schedule reasonably and economically and to avoid the body hurt and device damage. As a kind of important structure of vibrating screen, the lower crossbeam is the main carrying structure and it is easily damaged, so it is regarded as a researched object in this thesis and it is tested under the load in the laboratory. Based on the test, acoustic emission wave signals can be got-ten by modern acoustic emission testing technique. Then, the ?wavelet packet - energy? from the characteristics of acquiring signals is used as neural network input vector. In the BP network structure design, the design of a hidden layer with variable number of BP network is established. Based on the error by contrast, the best nerve number can be identified in the hidden layer. Through integrated analysis, using Levenberg-Marquard BP study algorithm, network-training errors are relatively small, the acoustic emission signal is used in BP neural network as a pattern of recognition. In Matlab6.5, neural network model identification is created and taking advantage of nonlinearity and the ability of learning and memory of Neural Network, this model is fixed by training structure of network with training samples. The work presented shows that acoustical emission signal processing and research on early fatigue fault diagnosis based on the wavelet and the neural network is viable.

Jan 1, 2014

Due to complex mineralogical and chemical interactions of the value and gangue mineral phases present in uranium-containing lateritic ores, deleterious pulp gelation which impacts on value metal recovery sometimes occur during atmospheric leaching. In this study, the leaching behavior and particle interactions of selected oxide (hematite, quartz) and clay minerals (muscovite, chlorite), which constitute predominant host gangue phases of typical lateritic uranium ores are investigated to provide basic, mechanistic understanding of temporal pulp gelation phenomenon. Isothermal, batch leaching with H2SO4 was carried out on concentrated dispersions (30 ? 57 wt.%) of single minerals at pH 1 and 25 or 70 °C and their concomitant solution, speciation and rheology (shear yield stress, viscosity) were characterized. It is clearly shown that despite the high oxide content of lateritic ores, the pulp chemistry and rheology is largely affected by the incongruent leaching behavior of more reactive, acid-consuming aluminosilicate clays. Furthermore, time- and temperature-dependent alumino-silicate species polycondensation interfacial reactions are shown to be responsible for the enhanced particle interactions, reflecting strong pulp rheology in agitation and pumping. If not properly mitigated, high pulp shear yield stress and viscosity have a striking impact on processability and hence, value metal recovery.

Sep 1, 2012

By I. Blayda

The purpose of this work is to study and make comparative analysis of germanium extraction and related valuable components of the sublimates from the burning of domestic power coals (product 1) and germanium sulfide materials, which are a waste of lead-zinc production (product 2), by traditional chemical methods (distillation of germanium in the form of tetrachloride from raw and preliminary burning source) and by microbial bioleaching of sulfur-oxidizing bacteria. The dependence of the germanium extraction by chemical methods from phase composition of the initial raw materials was installed. The germanium tetrachloride extraction from products 1 and 2 were 78.50 and 19.52%, respectively. Such difference in indexes on extraction, is caused by germanium confinement as concomitant trace component to the basic phases to carriers. The share of acid-non-soluble compounds (tetragonal modification GeO2 and silikogermanaties) in the product 1 account for 21.5 % of germanium. Ratio between acid-soluble and acid-not -soluble germanium forms are 19.52 and 80.48 %, respectively, in the product 2. Our experiments have shown, that implementation of restorative firing (with addition of 30-40 % carbon at 1150 0?) of sulfide product 2 considerably impacted on the extraction of germanium tetrachloride (91.76 %) in comparison with its low enough extraction at straight distillation of hydrochloric acid (19.52 %). The results are confirmed by a set of physical methods. The results of processing the same so-called hard phase?s material (product 2) with the help of microorganisms are presented. It Has been established, that selected strains of bacteria are capable of extracting from initial raw materials not only macro components (iron, zinc, lead, manganese, aluminum, nickel), but also micro impurity of rare metals (gallium, germanium, zirconium). It is important that these metals were not extracted by traditional chemical methods (with application of aggressive conditions and heats) independently of the phase composition of the source. Almost complete extractions of germanium in solution using sulfur-oxidizing bacteria take place in the first day of the process independently of the phase composition of the source and the type strain. The results have practical significance and can be the basis for developing a unified biotechnological method of technogenic waste processing with a purpose of their sterilization and detoxification with simultaneous obtaining concentrates of valuable metals. Keywords: germanium, extraction, sublimates, bioleaching, sulfur-oxidizing bacteria.

Sep 1, 2012

By I. Nishkov, I. Grigorova, M. Ranchev, S. Dzhamyarov

"Chelopech concentrator (part of Dundee Precious Metals) is located in central-western Bulgaria. The current process plant utilizes conventional primary crushing and SAG mill grinding, copper and pyrite rougher and cleaner flotation stages to produce a marketable gold-rich copper and pyrite concentrates. As in the most processing plants, the pyrite depression is carried out alkaline media using lime. The subsequent activation of pyrite mineral is achieved by adding sulfuric acid, which has an adverse effect on the flotation equipment. Therefore, a series of laboratory flotation experiment for activation of lime depressed pyrite by ammonium salts, such as ammonium chloride (NH4Cl), ammonium sulfate (NH4)2SO4 and ammonium bicarbonate (NH4HCO3), have been conducted. The obtained results showed that ammonium bicarbonate proved to be the most appropriate reagent choice for pyrite mineral activation. These results are confirmed by X-ray photoelectron spectroscopy (XPS), performed to determine the surface chemistry of pyrite in its natural state, after lime treatment and subsequent treatment by NH4HCO3. The registered XPS spectra indicate that the hydrophilic phases on the pyrite surface could be efficiently removed by using the ammonium salt NH4HCO3. The industrial use of NH4HCO3 as an activator of lime-depressed pyrite is a possible alternative for sulfuric acid replacement as a most widely used pyrite activator. Flotation experiments with addition of 200, 400, 600 and 800 g/t from each of the studied ammonium salts have been conducted. Furthermore, the impact of the flotation pulp pH within the scope of 9.00 – 10.50 was also investigated. The obtained results from the laboratory flotation experiments, showed that the pyrite activation with ammonium bicarbonate is an excellent possibility for replacing the sulfuric acid as main pyrite activator reagent, in order to eliminate the gypsum accumulation during the flotation of pyrite in Chelopech concentrator.INTRODUCTION The Chelopech deposit, located about 60 km east of Sofia is one of the largest Cu-Au deposits in Europe. The ore have complicated mineralogical and chemical composition. The main ore minerals are represented by pyrite, enargite (luzonite), tennantite, chalcopyrite and bornite. The average copper content of the mined ore is about 1.1 % and the gold content is about 4.0 g/t."

Jan 1, 2018

By Roberto C. G. Oliveira, Scott C. Brown, Brij M. Moudgil

The wettability or surface energy of particle surfaces dictates a number of multiphase ensemble interactions that have a significant impact in mineral processing. Dispersion, bulk powder handling and flotation behavior are just a few of the parameters that are largely due to the degree of hydrophillicity or hydrophobicity on particulate surfaces. Because of the inherent impact of surface wettability in nearly all industries, fields, and multi-phase interactions, a number of simple, precise and accurate techniques for accessing surface wettability or contact angle on macroscopic flat surfaces have been developed. However, these techniques cannot be directly applied to the particulate surfaces that are often in query. Though a number of techniques are available for accessing the wettability of particulate surfaces, these methods are either relative, application specific or prohibitively tedious. In this study, key features of existing techniques are combined to formulate an improved method to delineate particle wettability that is simple, versatile and capable of providing reproducible measurements in an industrial environment.

Jan 1, 2003

By M. M. Bugarin, P. J. van Staden, V. T. Conic, S. S. Dragulovic, R. M. Kovacevic, D. B. Milanovic

"The mineralogical and physico-chemical characteristics of a polymetallic sample from a mine of West Serbia suggest that it can be classified as a SEDEX type of ore. Those ores contain multiple value components, being inter-dispersed as fine grained aggregates. This prevents concentration by gravity or flotation concentration processes. Mineralogically, the valuable metals (Cu;Zn;Pb;Au and Ag) occur as pyrite, sphalerite, galena, tetrahedrite, chalcopyrite, covellite, arsenopyrite, and non-metallic minerals (barite, and waste minerals). Novel technologies are under development within this project for the recovery of all valuable metals from this very complex material. The work comprises the further treatment of solid residue obtained after Cu and Zn extraction by bioleaching, for the subsequent recovery of Pb and the precious metals Ag and Au. The residue is first treated with a saturated sodium chloride solution, whereupon a chloride solution of lead (NaPbCl3) is obtained. From the chloride solution, lead was deposited in the form of lead carbonate, followed by reductive melting, whereupon lead anode was obtained. Electrolytic refining of the lead anode, using a solution of PbCO3 in methane sulphonic acid (MSA-Methanesulfonic acid, min 99.5% CH4O3S, density 1.48 kg/dm3, Manufacturer: Carl Roth) as an electrolyte, yielded refined lead cathode. It should be noted that, after precipitation and separation of lead carbonate, the sodium chloride solution is restored to its original composition by the addition of make-up reagents and returned for another lead-sulfate leaching cycle. The solid residue obtained after leaching lead-sulphate, is leached in thiosulphate solution, with the addition of an activator, a catalyst and lixiviant for gold, to yield a thiosulphate solution of gold and silver. Since the content of gold and silver in solution is low (below 1 mg/dm3), they are first electrolytically concentrated on steel cathode and then refined to pure metals using well-known chemical methods. Note that, after the electrolytic separation of gold and silver, thiosulphate solution is recycled to the leaching step."

Jan 1, 2018