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By D. Pienaar, B. McFadzean, T. Jordaan

"Dithiophosphate (DTP) collectors have the lowest affinity for sulfide mineral surfaces compared to other common sulfide mineral collectors, such as xanthates and dithiocarbamates. In some cases it has been found that DTP does not adsorb onto the mineral surface at all and yet increases in recoveries and grades are noticed with the addition of DTP. Many studies have investigated the interactive effects of collector mixtures. However, there have been relatively few studies on the interactive effects between frother molecules and collectors. This study investigates the interactions between different types of frothers and sodium diethyl dithiophosphate.The study found that there were large increases in pyrite and galena microflotation recoveries at both pH4 and pH9 when DTP was mixed with small amounts of frother at a constant bubble size, showing that these increases were neither mineral-specific nor pH-specific. The same effect was not present when xanthate was used as a collector. The increases in recovery when using the DTP-frother mixture were similar irrespective of the type of alcohol or polypropylene glycol frother that was used. In an attempt to distinguish the mechanism of enhanced flotation recovery, various supplementary experiments were performed. It was found through adsorption experiments that no DTP was adsorbing on to the mineral surface. Therefore, interactions at the air-water interface were performed. Surface tension and critical coalescence concentration tests showed that, while DTP is a weak surfactant at the air-water interface, it does not have a synergistic effect in the presence of frother. DTP-frother mixtures do, however, show interactions in the froth phase, indicating an interaction in the thin films. It is proposed that there is a DTP-frother interaction on the bubble surface that enhances the rate of film thinning at the 3-phase bubble-particle contact."

Jan 1, 2018

By Kyle Bartholomew, Robert McIvor

"Functional performance analysis of closed circuit grinding provides valuable insight into the two components of ball mill circuit grinding efficiency: classification system efficiency and mill grinding efficiency. Classification system efficiency isolates the combined effect of classifier performance and circulating load ratio from other circuit variables, such as ore grindability and the mill grinding environment. Optimization of classification system efficiency ensures grinding energy is applied to particles needing further size reduction and not to overgrinding. Entirely based on size distribution data, classification system efficiency precisely distinguishes subtle changes in classification system performance. Use of the functional performance equation to isolate mill grinding efficiency allows for proper optimization of the mill grinding environment by isolating confounding effects of changes in classification and ore grindability. Variables such as mill percent solids and grinding media selection can be optimized using the mill grinding efficiency subcomponent of functional performance. First published by McIvor in 1988, the functional performance equation provides a set of standardized, quantitative optimization criteria, simple and powerful, which link circuit performance to plant design and operating variables that can be manipulated. Functional performance optimization has been applied in numerous mineral processing plants globally and continues to gain acceptance as a practical means for grinding circuit optimization. In this paper, examples of derivation and industrial application demonstrate the means by which functional performance analysis dissects grinding circuit efficiency into its subcomponents allowing the reader to apply this straightforward, powerful optimization methodology at their mineral processing operation."

Jan 1, 2014

By Paul Gottlieb

This paper reviews the status of automated applied mineralogy today and describes the history and fundamental theoretical and practical bases underpinning the development of automated systems. Details are given of the technical challenges that were faced in creating the new technology and in applying it to a range of applications. In recent years, automated mineralogy has become established as an essential enabling technology for the reliable acquisition of statistically sound comprehensive mineralogical and metallurgical data. This has had a revolutionary effect on the industrial use of such data in the study of geology, mining and mineral processing. Previously, using manual methods, it was not feasible to attempt this work because the large data sets required could not be assembled in a realistic timescale. There was a reliance on individual expert mineralogists and this was not scalable. The speed, reliability, detail and repeatability of the modern automated measurements has now made this type of analysis routine. Automated Applied Mineralogy has come of age! More than 100 systems have been installed around the World. Automated mineralogical analysers such as QEMSCAN® were originally developed as diagnostic metallurgical tools to improve mineral processing plants using samples drawn from plant surveys, bench and pilot-scale tests. They were used mainly for the assessment and auditing of size fractions of mill products, such as concentrates and tails. Subsequently, they began to be used for concentrator design and optimisation where ore characterisation was used to help understand the relationship between the feed ore and its subsequent behaviour in the plant. They are now widely used to measure exploration cores and drill chips from drilling programs to predict eventual metallurgical performance. Ore samples can be classified into metallurgical, as well as geological types, by combining mineralogical features in the ores with metallurgical properties related to grade control, separation, comminution, flotation and leaching behaviour. Three-dimensional block models of ore deposits are now being created based on processing response in addition to geological and mining properties. The development of automated systems began in Australia, the United Kingdom and Canada in the late 1970s and early 1980s. There were many technical challenges. Mathematical theories of randomness, sampling theory, image analysis and stereology were developed to ensure sample representivity so that meaningful information could be obtained. Sample preparation, presentation and measurement methods were developed to ensure that the random sampling was preserved during the measurements. Methods of automatic measurement and mineral identification evolved from the use of electron microscopes, fitted with backscattered electron brightness and energy dispersive X-ray detectors. Operational procedures were required to ensure that these instruments could accommodate a large number of samples and operate unattended for long periods of time. The new technology was progressively applied to a range of commodities and applications and new analysis methods, such as liberation measurement, were needed for metallurgical interpretation of mineralogical data.

Jan 1, 2014

By Scott C. Brown, Brij M. Moudgil, Ivan U. Vakarelski

The manipulation of the apparent hydrophobicity of particlute surfaces is necessary to achieve optimal selectivity in flotation processes. Previously a number of works have investigated the role of microscale surface and particulate morphologies on chemically modified substrates. These works have suggested that microscale surface asperities lead to an increase in flotation efficiency by assisting in the rupture of wetting films. Yet, in mineral processing the presence of surface asperities may lead to a reduction in flotation. The reason for this may-in part-be due to the presence of nanoscale irregularities at the interface. In this work, it is proposed that the presence of roughness at the nanoscale may have a dominant impact on the apparent hydrophobicity of mineral surfaces during flotation. It is suggested that as inter-asperity seperation distances are reduced capillary effects are enhanced for high energy mineral surfaces leading to the formation of liquid domains, which adversely impact hydrophobicity. In addition, as these distances approach the surfactant headgroup size obstruction of surfactant self-assembly process may occur, thereby further limiting flotation.

Jan 1, 2003

By F. Waanders, Campbell. Q.

This project was specifically aimed at using increased acceleration separation, as a method to optimize the recovery of gold in an ore body mainly consisting of hematite where the specific gravity of gold is much higher in comparison to the carrying material, making it possible to separate gold from other materials like silica, base metals and their oxides, usually associated with gravitation-gold-recovery-processes. The ore body investigated in this project originated from a gold reef containing a large portion of gold locked inside the gold pyrite complexes, which was mined and treated in a conventional way. After gold extraction, the material was pumped to a tailings dump and the gold extraction of this dump was investigated. In order to assemble a concentration plant setup, the head grade and size distribution of the dump and bulk sample were determined accurately. Chemical analysis and mineralogical examination were done on a representative sample of the bulk sample, to determine the chemical composition of the material. The results obtained thereof were evaluated and a pilot plant was configured. A bulk sample was processed in the pilot plant and the results were evaluated. The results at optimum acceleration forces applied, resulted in a recovery of 5% of the mass, with a gold concentrate of 90 g/t Au, which represented 58% recovery of the gold. The hematite with high specific gravity as main phase positively influenced the high acceleration separation process. It proved that if the specific gravity of particles in a suspension were increased, high acceleration separation could be applied effectively to separate much smaller particle sizes.

Jan 1, 2014

By M. Morales, J. Yianatos

"In this work, an alternative approach to evaluate the flotation performance along a flotation rougher row is presented. The collection zone as well as the froth zone performances were separately evaluated. For this purpose, sampling for metallurgical balances along with sampling of top-of-froth (TOF) grades in each cell of a flotation row were employed. The modelling of the rougher circuit consisted of using TOF grades for evaluating the collection zone recovery, because they are a good representation of the bubble loading, which identifies the true flotation process, as shown in previous studies for shallow froths. In addition, the feed characterization, size-by-liberation, allowed the identification of the mineral distribution and its evolution along the circuit. The latter result was obtained by fitting the recovery profiles as well as the TOF grades down the flotation bank. The flotation rates and the maximum recoveries in terms of size-by-liberation (size classes: -45 µm, +45-150 µm, +150 µm, and liberation classes: -20%, +20%-80%, +80%) were then estimated. The results were in good agreement with those reported in literature by other authors and showed the new approach allows flotation kinetics to be characterized in industrial circuits.INTRODUCTIONMineral recovery in industrial flotation circuits is a function of the mineral characteristics, such as particle size distribution and liberation (Trahar, 1981, Jameson, 2012), and operating conditions such as air flowrate, pulp flowrate, solids percent and reagent conditioning (Jameson 1977; Klimpel, 1980; Mehrotra and Kapur, 1974). The cell type and size (self-aerated or forced air) and the circuit arrangement (single cells or banks of cells in series) are also relevant factors. Sampling of circuits (e.g. rougher, cleaner or scavenger) are commonly carried out using standard automatic samplers for metallurgical balance assessment. However, the flotation plants are generally not provided with proper accesses for local streams, which hinders the recovery estimations and the flotation rate characterization."

Jan 1, 2018

By Adam Jordens, Olga Kuzmina, Christopher Marion, Kristian Waters

"In order to meet the growing demand for non-Chinese rare earth suppliers many new rare earth (RE) mineral deposits are currently under development, however these deposits typically include many minerals for which there is little processing information available. One of these deposits is the Nechalacho deposit located in the North West Territories of Canada. This deposit contains multiple RE minerals including bastnäsite, zircon, fergusonite, allanite and monazite. The work presented here investigates the use of different classes of flotation collectors (carboxylic acids, hydroxamic acids, phosphoric acids) typically used in RE mineral flotation to float the Nechalacho ore directly. Flotation tests are also conducted as the final step in a beneficiation process incorporating centrifugal gravity concentration and magnetic separation. This combination of centrifugal gravity concentration and magnetic separation rejects low specific gravity gangue minerals such as K-feldspar and plagioclase and concentrates high specific gravity minerals such as magnetite and hematite. The removal of low specific gravity gangue helps to improve flotation and the removal of ferromagnetic iron oxides is important prior to flotation using certain chelating collectors."

Jan 1, 2014

By Stoyan N. Groudev, Ioannis Paspaliaris, Irena I. Spasova, Kostas Komnitsas

"Acid mine drainage waters generated in the uranium deposit Curilo, western Bulgaria, were treated by means of a constructed wetland located in the deposit. The waters had a pH in the range of about 2.5 - 4.1 and contained uranium, radium, some heavy metals (iron, manganese, copper, zinc, cadmium, cobalt, nickel, lead), arsenic and sulphates in concentrations much higher than the relevant permissible levels for waters intended for use in the agriculture and/or industry. The wetland covered an area of about 140 m2 and was characterized by an abundant water and emergent vegetation and a diverse microflora. Typha latifolia, Typha angustifolia and Phragmites australis were the prevalent plant species in the wetland but species of the genera Juncus, Eleocharis, Scirpus, Carex and Poa as well as different algae were also well present.The water treatment was started in July 2001 and until now (August 2002) the wetland effluents were characterized by pollutants concentrations decreased below the relevant permissible levels. The water flow rate through the wetland during this period varied in the range of about 0.2 - 1.0 l/s. The water clean-up markedly depended on the temperature but was efficient even in the cold winter months at air and water temperatures close to 0oC. The removal of pollutants was due to different processes but the microbial dissimilatory sulphate reduction and the sorption of pollutants on organic matter (viable and dead plant and microbial biomass) and clay minerals played the main role. Negative effects of the pollutants on the growth and activity of the indigenous plant and microbial communities were not observed."

Jan 1, 2003

By J. B. Rubinstein

"The paper gives an overview of the history of flotation machine development. The laws of their evolution are stated and the place and role of column flotation are demonstrated.The major parameters of column cell diameter and height are discussed. Options are proposed for optimization of the hydrodynamic characteristics of large-capacity column cells. The high efficiency of columns with cell height of 4-6 m is demonstrated. The optimum parameters of multisectional column machines are determined. Their advantages compared to monocells are shown. A scaling-up procedure for column machines was developed based on flotation macro- and microhydrodynamics simulation."

Jan 1, 2003

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 P. Saha, D. M. Chakrabarti, J. P. Srivastavam, P. Bhattacharyya, B. R. Sarkhel, Banerjeem B.

The phosphatic soil deposit at the Sukulu hills region of Uganda contains 10-12% P2O5. The ore occurs as a naturally degraded soil deposit containing a very sticky slime composed of earthy lateritic minerals. Desliming of the ore, which is imperative for its further beneficiation, is an extremely difficult hurdle to overcome for its commercial utilisation. Earlier studies on samples of the same ore at the National Metallurgical Laboratory (NML) and abroad established that it was necessary to pass the ore through a series of three stages of desliming, each consisting of a step of vigorous attrition scrubbing followed by hydrocycloning, for effective elimination of the sticky slime. In the present paper an innovative use of the very strong shear-fields created inside a hydrocyclone has been discussed, that could effectively eliminate the stubborn slime from the ore. The standard design of the hydrocyclone was suitably modified to increase the shearing effect on the slurry. It was possible, through the application of this modified hydrocyclone, to not only totally eliminate all the stages of attrition scrubbing, but also to reduce the subsequent stages of hydrocycloning. The modified technique yielded a concentrate of grade comparable to that obtained by employing the earlier more complex flow sheet, with about 25% higher P2O5 recovery.

Jan 1, 2003

By K. Price, G. Wang, L. R. Moore, Y. R. Xiong, J. Gu

"Sand is a naturally occurring granular material that is a result of the physical or chemical breakdown of rocks. Raw/natural sand contains various minerals, and it is this combination of minerals that brings the value to the construction aggregate industry. However, it is the quartz component of sand that is valued in its application as industrial silica in glass, high purity quartz, foundry sand, and oil and gas fracturing. Depending on the industry, the grade requirements can be the concentration of SiO2, particle size or shape, as well as contaminants such as the heavy refractory minerals, clays, fines, and alkali metals. With the ever declining mineral feed grade, processors continue to face challenges making the industry specific concentrate grade. As such, it becomes more important to tailor make the processing reagents to fit the mineral, processing conditions, and desired quality specification. This paper focuses on the application of novel collectors towards the beneficiation of sand for each of the major industrial silica applications. INTRODUCTIONQuartz is a mineral composed of a framework of silicon and oxygen atoms. It is the second most abundant mineral in the Earth’s continental crust. There are many species of quartz, which are defined by the particle size, shape, and color. Silica sand is one of those species, which is the byproduct of the physical or chemical breakdown of quartz containing rocks or crystals. Geologist define silica sand as a silica mineral with a particle size between 0.05 and 2 mm in diameter (Zdunczyk, 2001). Silica sand has significant value to society in recreation (beach sand and toy boxes), construction aggregate (concretes and asphalt), industry (iron & steel casting, fracturing proppants, and glass), as well as specialty products such as semiconductors or silicon wafers used in electronics.The aggregate business is the dominant consumer of silica sand products. Conversely, glass making, foundries (casting material), abrasives, and fracturing proppants are the dominant applications for industrial silica sand. Not much beneficiation is required for sand products going into the construction industry, other than sizing and scrubbing to remove clay. However, the industrial silica sand applications are dependent on particle size, shape, and degree of contaminants, which sets the market value (table 1). Therefore, as the more specialty products are produced, more sophisticated techniques and chemistry need to be applied to ensure the appropriate quality is met."

Jan 1, 2018

By Takashi Furuyama, Sukeyuki Mori, Tetsuo Ikejiri, Abel Bissombolo, Yoshitsugu Koga, Masamichi Hata

In Japan, the increasing number of automobiles newly put into circulation is followed by a larger amount of end-of-life vehicles from which valuable metals are being recovered in shredder and related plants. Nevertheless, the processing of these scrapped automobiles which has reach a recycling rate of about 75%, generates a huge volume of waste, locally known as .shredder dust., which is commonly dumped on landfills. The saturation and depletion of valuable disposal sites in the near future, as well as the social and environmental problems related to the accumulation of these residues disposals are a major challenge for the automobile shredding industry. To promote an alternative way for the management of these disposals, the authors have initiated and developed a system for their processing, on the basis that more than 90% of these residues are combustible materials that could be used as refuses derived fuel. The developed processing system points out the mechanical/physical separation of shredded automobiles residues into two streams by means of an ascending airflow passing through a vertical zigzag separator and, the compaction of the light-density fraction of materials (that is about 60% of auto shredder residue recovered as float products and mainly composed of cotton, sponges and light plastics) to form a refuse derived fuel (RDF), the density, calorific value and ignition loss of which are 1.19 g/cm3, 4470 kcal/kg and 60.7%, respectively.

Jan 1, 2003

By D. B. Mazzinghy, L. C. de R. Machado, H. Delboni, M. G. Bergerman

"The use of vertical stirred mills in the mining industry has increased remarkably over the past few decades, as a result of growing requirement for finer ore grinding. This equipment delivers higher energy efficiency in fine grinding operations when compared to conventional tubular mills. Methods for designing vertical stirred mills involve operational experience, pilot plants and bench tests. An important issue is that these tests require, at a laboratory scale, at least 10–20 kg of material, depending on its density, which is not available in many cases, particularly in the early stages of greenfield projects. For the regrind of flotation concentrates, several bench scale flotation cycles are required to generate such a sample. This paper describes the development of a laboratory jar mill test using a 6”x8” jar – smaller than that commonly used – based on the overall specific energy method, which requires significantly less mass compared with existing tests. The proposed test has proven to be more practical than tests normally used, requiring about a quarter of the mass, and also shows good adherence to industrial results for the studied iron ore processing plant. INTRODUCTION A significant demand for finer grinding has been noticed over the past few decades in several mining projects to achieve the mineral liberation required for the concentration of valuable minerals. However, the finer the product size, the greater the grinding energy consumption, resulting in an overall increase in operating costs, which may reach or even exceed 50% of the mineral processing cost (VIEIRA, PERES, 2013; DANIEL, LEWIS-GREY, 2011). Comminution technology can have a major impact on subsequent ore concentration stages (DANIEL, LEWIS-GREY, 2011; MARSDEN, 2009; NAPIER-MUNN, 2012; PEASE et al., 2010), which further strengthens the importance of proper technology and equipment selection. Adequate grinding circuit selection and design is thus a key aspect associated with mining projects."

Jan 1, 2018

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 A. P. Wang

Porous carbon adsorbents derived from inorganic materials templates such as zeolite and mesoporous silicate attracted considerable attention in the last decade and got great progress in re-cent years. However, so far almost all of templates used in the process were artificial porous materials; the porous carbons prepared by this method are very costly, which restricts the synthesis and application of templated porous carbons. In order to reduce the cost of templated porous carbons, natural inorganic porous minerals have been taken into consideration, which maybe possible and promising templates to prepare carbon adsorbents. In this work, we describe template process using tubular halloysite, rich mesoporous zeolite and low bulk density diatomite, as exemplars of the categories of inorganic porous templates which we have studied and discussed the effects of different templating structure on the resultant carbons. Two main carbon precursors, sucrose and furfuryl alcohol, were used respectively. The morphology of minerals and corresponding templated carbons were characterized using electron microscopy. The pore structures of minerals and templated carbons were characterised with nitrogen adsorption. The results showed that the morphology and pore structure of porous carbons are in good pertinence to those of corresponding templates. The morphology and pore structure of templated carbons could reflect those of corresponding templates at nanometer level. The templated carbons with high specific surface areas and rich mesopores can be prepared by using these three kinds of natural porous minerals as templates. The higher the surface area and pore volume of the minerals, the higher those of the corresponding carbons. The template carbons from halloysite possessed higher pore volume and mesoporosities. Based on the large mounts of experiment results, a model for the mechanism of resultant nanopores formation has been proposed. The nanopores of templated carbons are mainly composed of three kinds of pores: templated pores formed by removing mineral, hereditary pores formed by inheriting the pores of templates and nanopores formed during carbonization. These three kinds of pores have a close relationship with corresponding template.

Jan 1, 2014

By Herman Mendoza, Luisa Ciriaco

An investigation of the seeding mechanism using heterocoagulation and the Derjaguin - Landau - Verwey - Overbeek (DLVO) theory of two pure minerals is the objective of this study. The seed was silica with modal diameters of 4.529 µm (fine particles) and 5.216 µm (coarse particles) and the test powder was hematite with a modal diameter of 0.883 µm. Parameters included variations in the concentration and particle size of silica. Both particles were first subjected to size determination and settling tests via Stoke’s Law. The silica-hematite system was then suspended in 0.001 M KNO3 electrolyte solutions where pH was adjusted. Afterward, the suspension was agitated and was allowed to settle at different time intervals while obtaining turbidity readings. Results through settling time and turbidity vs. pH graphs indicate that maximum heterocoagulation occurs from pH 2 to 5 while minimum heterocoagulation occurs from pH 6 to 7. At these pH levels the zeta potentials of silica and hematite are negative and positive, respectively. On the contrary, repulsive forces dominate the system from pH 8 to 11 due to the particles’ negative zeta potentials. Furthermore, the attachment of hematite to silica increases when the parameters become larger thereby increasing the effectivity of heterocoagulation at acidic to neutral pH levels.

Jan 1, 2014

By Andrzej Luszczkiewicz, Alicja Bakalarz

The application of new collectors is considered to improve the beneficiation of Polish sedimentary complex copper ores from the Legnica-Glogow Copper Basin (SW Poland), the upgradeability of which becomes more difficult because of ores grade declining. One group of potential collectors is represented by nonpolar reagents. According to the available literature data, only selected sulfides float in the presence of the nonpolar liquids. The paper presents laboratory scale flotation results for the main sulfide minerals occurring in the Polish copper ores applying either thiol (potassium ethyl xanthate) or nonpolar (aqueous emulsion of n-dodecane) collectors. The investigated feed contained 1.91 % Cu in the form of sulfide minerals such as bornite, chalcopyrite, chalcocite and covellite. Other sulfide minerals including galena, pyrite and sphalerite were also present in the samples. Several flotation tests with various doses of each collector were conducted. Mineralogical analyses of flotation products were carried out and the results compared. A comparison of the results indicated that all sulfide minerals floated well with high recoveries ranging from 91 % to 99 % in the presence of the thiol collector. The use of the nonpolar collector provided results in flotation of sulfide minerals with different terminal recoveries from 61 % for chalcopyrite to 100 % for sphalerite. The most significant differences in flotation in the presence of both types of collector under various conditions of upgrading were observed for chalcocite, chalcopyrite and covellite. Similar flotation results were observed for sphalerite and galena for both collectors. The studies confirmed selective flotation of sulfides from the copper sulfide ores of the Legnica-Glogow Copper Basin in the presence of nonpolar collectors.

Jan 1, 2014

By Ghislain Bournival, Cagri Emer, Seher Ata

"It is well known among flotation practitioners that the contact angle can be correlated with the amount of material recovered from feed by flotation. The contact angle of solids can easily be modified by the addition of a collector. However, some collectors also have frothing properties thus altering the solid and bubble surface properties simultaneously. To avoid this problem, a technique has previously been used in which silanol groups are attached to the surfaces of the particles, but this method has its own problems. In this work, silica particles with various surface hydrophobicities were prepared using an esterification process. By using alcohols with different hydrocarbon chain lengths, from 4 to 12 carbon atoms, surfaces with a wide range of contact angles could be prepared. The technique was used in the modification of silica particles that were tested in a fluidized bed flotation column, and a laboratory mechanical flotation cell. In parallel experiments, dodecylamine (DDA) was used as a collector. It was found that irrespective of the type of flotation machine and surface preparation method, there was a close correspondence between flotation recovery and the contact angle of the particles. The silanation process has known drawbacks relating to the presence of moisture during the reaction, and the stability of the silane coating after it is been prepared. Esterification does not suffer from these disadvantages. This work has shown that the esterification technique is a robust alternative method for preparing hydrophobic quartz surfaces."

Jan 1, 2014

By K. Saberyan

In this study, solvent extraction of zirconium by using triphenylphosphine oxide as extractant has been investigated. The results showed that extraction of zirconium by triphenylphosphine oxides in nitric acid and hydrochloric acid media were negligible. Extraction of zirconium in acetic acid media with concentration of 0.01~0.2 M has been studied and the results showed that the maximum percent of zirconium extraction was 40% in acid acetic with concentration of 0.01 M. By addition complexing agents such as potassium thiocyanate with the concentration of 0.01~0.2 M zirconium extraction increased up to 86% in 0.2 M potassium thiocyanate. By addition of sodium salicylate with concentration of 0.01 M and in pH=2.5, the maximum extraction of 96% was achieved. The striping of zirconium from organic phase can be carried out by 0.5 M solution of sulfuric acid.

Jan 1, 2014