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By Felipe Henríquez, Daniel Silva

"Traditionally, the implementation of an automated advanced process controller in any mineral processing complex is a challenge, mainly due to the quality of resources and technologies required, the uniqueness of each control solution and the uncertainty of the engineering hours needed to complete the task. Thus, the use of advanced and proven control technology becomes a key factor when deploying the control strategy. However, success would still not be possible without the presence of common sense, process knowledge and fundamental process data. Minera Los Pelambres, taking advantage of such factors and its accumulated process experience, implemented a novel and successful combination of MPC (Multivariable Predictive Control) and advanced control for secondary grinding and regrinding stages at its copper concentrator plant. In both cases, the control objectives are: being capable of processing a variable feed from the upstream process while at the same time avoiding to become a process bottle neck and yet, maintaining an adequate product quality (in terms of size distribution) to the process downstream. Additionally, for the case of the vertical regrinding mill (vertimill), the control system should also be capable of keeping an adequate circulation load and making an efficient use of the available grinding power. In either case, extending hidrocyclones availability while maintaining their performance is a must, since both factors are required for process and maintenance purposes. Thus, the process control problem becomes one with a multi-variable type of process with multiple control objectives to satisfy simultaneously. In trying to solve it, many mineral processing operations have implemented basic or conventional control or even better yet, expert systems. Minera Los Pelambres believes that better and faster results can be achieved using a combination of MPC and advanced control. Such strategy was successfully implemented, reducing considerably process variability while maintaining high throughput and keeping the process well within constraints limits. Their control philosophy, implementation process, main results and their key performance indicators are discussed here."

Jan 1, 2014

By Bent Babel, Martin Rudolph

"The characterization of reagent-mineral interactions in flotation systems of finely intergrown ores holds difficult challenges for the applicability of standard techniques like Hallimond tube tests and contact angle experiments or renders them impossible due to a lack of sufficient samples in terms of quality and quantity. This disadvantage may not apply to more sophisticated techniques, but these often do not work in an aqueous environment. We present the utilization of an atomic force microscope with a hydrophobic colloidal probe to characterize the wettabilities of individual mineral domains of an ore sample, while additional spectral information is gathered by Raman spectroscopy. The exemplary ore sample investigated is mainly containing cassiterite and quartz, therefore the reference measurements like Hallimond tube tests and contact angle experiments were carried out with this binary system as a comparison. The focus of the study lies in the correlation of data gathered by the atomic force microscope and the Raman spectrometer with data from standard techniques. Finally, the applicability of the colloidal probe atomic force microcopy technique for reagent-mineral investigations is critically evaluated.INTRODUCTIONThe focus of this paper is the application of colloidal probe atomic force microscopy (CP-AFM) for theinvestigation of reagent-mineral interactions on a binary system of cassiterite and quartz. This and similar concepts using hydrophobic AFM probes have been applied by multiple authors (Rudolph and Peuker, 2014a; Rudolph and Peuker, 2014b; Wada et al., 2017; Xie et al., 2017). The hydrophobic interaction is the main interacting mechanism for the hydrophobic colloidal probe with hydrophobic sample surfaces and the long range attractive component has been accounted to nanobubbles on the interacting surfaces (Yakubov et al., 2000). More detailed information on nanobubbles are available in two reviews compiled by Attard and Hampton (Attard, 2003; Hampton and Nguyen, 2010). This paper is based on the work by Rudolph and Peuker comparing different AFM based measuring concepts, additionally gathering data with Raman spectroscopy and correlating results of microflotation and CPAFM measurements (Rudolph and Peuker, 2014a; Rudolph and Peuker, 2014b)."

Jan 1, 2018

"Wet low intensity magnetic separation has been used for the recovery of magnetite for decades. As high-grade reserves continue to decline, low grade magnetite ores are being targeted for iron production. Low grade magnetite mineralisation is typically fine grained and requires fine to ultrafine grinding (P80 40 - 30 µm) to liberate it from, predominantly, silica/silicate gangue matrices. Grinding to such particle sizes requires high power consumption and produces excessive fines which impact negatively on wet magnetic separation and tailings dewatering. In addition, the dearth of fresh water for mineral processing in arid areas impacts negatively on the economic viability of low grade magnetite projects. These challenges have motivated innovation in dry magnetic separation technologies for the beneficiation of magnetite that can be economically applied on a large-scale. Such technology has been developed in the Cyclomag Planar magnetic separator (PMS) invented by South Australia-based Christopher Kelsey of IMPTEC P/L. The significant gangue mineralisation associated with magnetite ores in South Australia is quartz. In this study, the performance of the Cyclomag PMS on the recovery of magnetite mineral from magnetite-quartz blends was investigated. Magnetite-quartz blend were subjected to the PMS at varying control parameters - magnet discs rotation speed, inlet airflow and feeder speed. The study showed a successful dry separation of magnetic mineral from non-magnetics using the Cyclomag PMS. The PMS has potential to effectively recover magnetite mineral."

Jan 1, 2018

By P. Latostenmaa, T. Hailemariam, M. Lundström, P. Halli

Doré process is unique way to treat precious metals in the copper electrorefining plant, since it uses anode slime as a raw material. In this pyrometallurgical process, also slag is produced together with Doré metal. However, the process is never ideal, and a part of metal is always lost into the slag. By using Doré slag as raw material for simply mineral acid leaching, some of the lost elements can be extracted and recovered, thus, increasing the sustainability and keeping metals in the circular economy loop. The Doré process itself is developed to convert almost all precious metals and PGMs in the Doré metal, leaving other elements into the slag fraction. The Doré slag consist of slag formers, such as borax and silica based minerals, but contain also traces of sealing materials. In addition, the Doré slag is rich in metals present in the anode slime, such as Cu, Bi and Sb, which are not converted into the Doré metal. There are only few published applications at the precious metal plants, where conservative grinding and flotation circuits have been utilized for the enrichment of valuable metals present in the Doré slag fraction (Godbehere, P.W., 1983; Segawa, C. and Kusakabe, T., 1996). However, the present study shows an alternative approach for the recovery of metals present in the Doré slag by hydometallurgical approach. The study focus on direct mineral acid (aqua regia) leaching of metals present in the Doré slag. The initial dissolved concentrations of Cu, Bi and Sb from Doré slag in the temperature range of 30-50 °C under oxygen purging with addition of 1 vol-% of H2O2 are presented. Chemical and mineralogical analyses were performed for the raw material, leaching residue, and leaching solutions in order to ascertain the leaching behavior of the metals of Bi, Cu and Sb.

Jan 1, 2018

By C. A. C. Sequeira, G. N. Anastassakis

"The separation of fine or even smaller size mineral particles with conventional methods is inefficient due to the specific properties of fines (small mass, high specific surface area, and high surface energy per unit area). Hence, the production of high-grade concentrate with high recovery is very difficult to impossible and a significant share of mineral values is lost to the tailings. The aim of the current research is to investigate the possibility to efficiently separate value minerals from gangue of fine particle size. The objective of the current work is to develop separation schemes of fine mineral particles by combining an initial stage of particles agglomeration with the use of collectors (hydrophobic agglomeration) with a subsequent conventional separation method. In the current research, magnesite was used as mineral value to be separated: a) from quartz, and b) from mineral mixture (serpentine, ilmenite, and olivine). In each case, tests on single minerals and artificial mixtures were carried out. After hydrophobic agglomeration, the separation of magnesite from quartz was achieved by settling; in the second case (gangue: serpentine, ilmenite, and olivine), magnetic separation of the co-agglomerated gangue was applied. In both cases, the results of the preliminary tests on single minerals suggest that the separation of mineral value is feasible and efficient. These findings were also confirmed from the results of the tests on artificial mixtures of magnesite and gangue, either quartz only or mineral mixture. Both separation schemes provided with magnesite concentrates of commercial grade (95% magnesite) with high recovery. INTRODUCTION The generation of fine particles is inevitable in many operations of mineral commodities processing. Especially in the case of low-grade ores, the mineral value is finely disseminated in the ore, and considerable liberation occurs at a fine size range. Although there is not a uniform classification system with respect to mineral particles size, fines are usually characterized the particles with a size range of -100µm+20µm, very fines those of -20µm+5µm, ultra fines of -5µm+1µm, and colloids smaller than 1µm (Sivamohan, 1990)."

Jan 1, 2018

By John Ralston, Jona Addai-Mensah, Patience Mpofu

The flocculation and dewatering behaviour of kaolinite (non swelling) and smectite (swelling) clay dispersions has been investigated using hydrolysable metal ions Mn(II) and Ca(II) and anionic polyacrylamide-acrylate copolymer (PAM) at pH 7.5 and 10.5. A pH-dependent, specific metal ion adsorption behaviour, accompanied by a marked reduction in particle zeta potential and slurry shear yield stress, was observed to have a profound influence on the colloid stability of both types of clays. Due to the differences in the cation exchange capacity, the smectite clay dispersion required a higher amount of metal ions than kaolinite dispersion to produce similar effects. The adsorption density of the anionic PAM at the negatively charged clay particle surfaces correlated well with metal ion hydrolysis and adsorption behaviour, all of which had a strong effect on slurry settling rate and extent of consolidation. At pH 7.5 where Mn(II) ions hydrolyse, metal ion and flocculant adsorption densities were both greater in the presence of Mn(II) than Ca(II) ions. At pH 10.5, however, where Ca(II) ions begins to hydrolyse, higher adsorption densities were observed for Ca(II) ions in comparison with Mn(II) ions, as the latter hydrolysed completely and precipitated. The metal ion mediated flocculant adsorption led to improved hydrogen bond driven particle bridging and facilitated charge neutralisation flocculation mechanisms which significantly enhanced the dewaterability of both clay dispersions.

Jan 1, 2003

By Wang Xu, Tao Dongping, Zhang Jie, Tao Youjun

Based on the principle of fly ash triboelectrification, the mineral electrical index and testing method are introduced. The electric differences of various mineral components of fly ash are discussed in view of the results of chemical and mineral composition analysis of the fly ash sample acquired from the Xin-wen power plant. The dielectric constant and charge-mass ratio of carbon and ash in the fly ash are determined. The data were then used along with the rotary triboelectrostatic separator (RTS) testing results to investigate the charging characteristic of fly ash particles in different sizes. The results show that the dielectric constant of fly ash with different particle size decreased with the decrease in particle size, which led to a poor electrical conductivity. Thus particle size has an important effect on conductivity. The charges of carbon and ash particles increased with decreasing particle size. The charge-mass ratio of carbon and ash particles of the same size increased with decreasing particle size. This indicates that finer particle size is more favorable for triboelectrification separation from the charging efficiency point of view. The rotary triboelectrostatic fly ash separation tests show that the best decarbonization performance was achieved with particles in the size range of 0.038-0.074mm with which the decarbonization rate and efficiency index reached 38.93% and 120.83% spectively.

Jan 1, 2014

By W. Pawlos

"The paper will present the methods of visual observation and recording of movement paths of coal grains of different physical properties in the paramagnetic liquid. The paths were recorded with a video camera in the working chamber by means of a specially constructed device, acting as a periscope, which were then transformed into digital images.Experimental movement paths were confronted to the paths obtained in a theoretical way by means of solving differential equations of movement. The outlet level of a grain of the same physical properties from the separator is a random variable with normal distribution which modal value is equal to the outlet level of a spherical grain, calculated from the solution of grain movement equations. At these assumptions it is possible to calculate the height of the passage from the separator working chamber to separate a given product with a given separation accuracy, measured by a probable error and to determine separation conditions."

Jan 1, 2003

By A. Mainza, I. Govender, J. Waters

"The study of the properties of mineral processing suspensions is important in understanding how a circuit might behave. As soon as the predominantly dry ore enters a wet milling stage the ore properties undergo changes as a ‘slurry’ is created. Slurries can be classified in terms of their physical properties (particle density, solids concentration, particle size and size distribution, particle shape), and their flow properties such as rheology. Slurry flow regimes are classified into true homogeneous, pseudo homogeneous, heterogeneous and fully segregated, and only true homogeneous and pseudo homogeneous suspensions can be characterized by their flow structure. A class of the heterogeneous regime are the so-called dense phase or settling slurries - those which result in a clear water surface on standing, although they may approach a pseudo homogeneous state if suspended for a sufficient period of time. They are usually extremely difficult to characterize by their rheological properties alone and the rheological characterization of these slurries has always posed a problem, especially at higher concentrations. Previous rheological studies have focused on the individual concentrator units dealing with milling, classification, pumping, flotation, fine grinding, thickening.In this work an attempt was made to characterize two ore types (copper and a Platreef platinum ore) using a custom built Paterson and Cooke tube rheometer, at concentrations up to 43% by volume. After applying a turbulence correction, results showed Bingham plastic behavior. A conventional vane rheometer was then used to compare the rheological behavior of platinum concentrator streams. A size criteria was used to identify any rheologically dominant streams."

Jan 1, 2014

By C. Dorfling, W. A. Rossouw

"Hydrometallurgical processes used for metal recovery from waste printed circuit boards (PCBs) typically involve dismantling, shredding and physical separation prior to successive leaching stages for selective dissolution of different metals. The principles of the physical separation units are well understood, but valuable metal losses of more than 30 % can be incurred during these processing steps. The impact of the physical separation units’ performance on downstream leaching operations have not been defined; this prevents the development of a well-integrated process. The objective of this project was to determine to what extent the base metal leaching behavior depends on the physical separation pre-treatment. PCBs were shredded to 100 % passing 2 mm before physical separation by dense medium separation (DMS) as well as magnetic separation. Batch leaching tests using various concentrations of sulfuric acid were conducted on three feed fractions: (1) shredded PCBs without any physical separation, (2) heavy fraction recovered from DMS, and (3) non-magnetic fraction recovered from the DMS heavy fraction. DMS increased the metal content in the feed from 48 % to 75 % on a mass basis, but 70 % of the gold and 20 % of the copper reported to the light fraction. The application of magnetic separation to the heavy fraction produced by DMS removed 67 % and 61 % of the iron and nickel, respectively, while negligible amounts of non-magnetic metals were removed. Although DMS successfully concentrated the feed and magnetic separation removed the majority of iron and nickel, these steps did not result in any improvement in the rate or extent of copper leaching. Metals generally leached faster when the sulfuric acid concentration was increased from 1 M to 2.5 M; this effect was seen to be more pronounced for pretreated feed. INTRODUCTION The fast rate of technological development has led to a decrease in the service life of electronic devices. This is resulting in an increased rate of electronic waste generation. The recovery of metals from electronic waste is of environmental and economic interest. The majority of these metals are typically located on printed circuit boards (PCBs) within electronic devices (Tuncuk, Stazi et al., 2012). Hydrometallurgical processes are considered a viable option for small scale metal recovery from waste PCBs, and generally involve the following steps: disassembly for removal of hazardous and reusable parts, size reduction, physical separation, successive leaching stages for metal dissolution and finally recovery of metals from leach solutions."

Jan 1, 2018

By G. P. Karmakar, K. K. Chandan

"The drilling mud is an essential part of the drilling process, which plays a major role in keeping safe and efficient oil and gas well drilling. In the oil industry, bentonite clay dissolved in water produces the simplest type of drilling muds. Bentonite clay contains montmorillonite particles. These particles are dispersed uniformly in water and such dispersions are used in various industrial products like paints, ceramics, pesticides and drilling muds. The bentonite clay easily dissolves in water and increases the viscosity of the water, which is one of the most important properties of a drilling mud. Bentonite has the highest swelling capacity, which is responsible for building up of the viscosity of the clay-water system. The flocculation behavior of bentonite is one of the major concerns for the performance of the water-based drilling mud in the oil and gas well drilling process. The behavior of drilling mud greatly depends upon the quality and quantity of bentonite clay, as well as the additives that are used in their formulations. In this work, a comprehensive study has been carried out to find out the effect of added polyacrylamide (PAM) polymer, surfactant, pH and salt concentrations on the dispersion/ flocculation characteristics of bentonite clay-water system. It has been observed that the increase in PAM dosage reduces the residual turbidity and improves the settling rate of the bentonite particles. The flocculation rate has also been found to be better under higher pH conditions. The combined effect of salt concentration and PAM dosage improved the overall flocculation efficiency of the system.INTRODUCTIONIn the oil industry, bentonite clay dissolved in water produces simplest type of drilling muds. Bentonite clay containes montmorillonite particles. These particles are dispersed uniformly in water. Such dispersions are used in various industrial products like paints, ceramics, pesticides and drilling muds (Akther et al., 2007). The bentonite clay easily hydrates in water and increases the viscosity of the mud system (Razi et al., 2013; Meng et al., 2012). Bentonite clay in the drilling mud increases the viscosity which is one of the most important prop erties of a drilling mud. Bentonite has the highest swelling capacity, which is responsible for the building up viscosity of the clay-water system (Sonmez et al., 2013). The drilling mud is an essential part of the drilling process, which plays a major role in keeping a safe and efficient oil or gas well drilling (ASME, S. S. C., 2005). The flocculation behavior of bentonite is one of the major concerns for the performance of the water-based drilling mud in the oil or gas well drilling process. This behavior of drilling muds greatly depend upon the quality and quantity of bentonite clay, as well as the additives that are used in their formulations (Yu and Amanullah, 2005; Akther et al., 2007). Bentonite particles form aggregate under certain conditions including high temperature, and high concentration (Luckham and Rossi, 1999). If the quality of bentonite is not sufficient to accomplish intended viscosity of the muds, it is essential to add certain additives to increase the viscosity and prevent aggregation of the system (Razi et al., 2013). The anionic polymer bearing sample can build up inter-particle bonds between the polymer and clay particles. The addition of various additives like, polymers control the dispersion and enhance the viscosity of the mud by controlling the flocculation of montmorillonite particles in bentonite dispersion (Heller and Keren, 2002; Mahto and Sharma, 2004)."

Jan 1, 2018

By Daniel Saramak

"Issues concerning effectiveness of the high-pressure comminution process in technological circuits of copper ore treatment were presented in the paper. Crushing processes taking place in high-pressure grinding rolls devices (HPGR) are currently one of the most efficient methods of hard ore size reduction in terms of the energy consumption. The HPGR products are characterized by a fine particle size and the micro-cracks formation in individual particles, which appear in downstream grinding processes, decreasing their energy consumption. The purpose of this paper was to analyse the effectiveness of a ball mill grinding process depending on the changeable conditions of run for the HPGR crushing process. The research programme carried out included crushing tests in the laboratory scale HPGR device at various settings of the operating pressure volume and selected qualitative properties of the feed material (i.e. particle size distribution). Particle size distribution analyses of all HPGR products were performed and in the next stage the material was a feed to the ball mill grinding process. Grinding process kinetics were investigated through the determination of mass recoveries of individual particle size fractions after defined grinding time intervals. The models, defining the grinding process effectiveness as a function of changeable conditions of HPGR process run, were determined on the basis of obtained results. Based on these models the optimal grinding time in a ball mill was specified which is, in turn, the basis for optimization of operation of the technological comminution circuits for a given material type. The obtained results proved that the application of HPGR devices in a given copper ore comminution circuit may improve the effectiveness of the downstream grinding process which leads to improvement of the entire circuit work efficiency through decreasing the process energy consumption and enhancing product size reduction."

Jan 1, 2014

By Felipe Sepulveda, Edelmira Gálvez, Luis Cisternas

"In mineral processing, the recovery and/or concentration of the value components cannot occur in one operational stage, therefore requiring the use of separation circuits based on several flotation stages. The components to be separated are typically distributed at different concentrations and different particle sizes, resulting in different levels of recovery. Typically, more than one value component must be selectively removed by exploiting the differences in the components’ floatability at different pH values, pulp potential and particle size. Several methods for the design of these circuits are available in the literature, but comparatively few studies present circuit analysis tools or address the design of a multiple-product flotation circuit. In this study, global sensitivity analysis was used to analyze a flotation circuit with several products, such as copper, lead and zinc. This analysis was based on the Eureka mine concentrator plant. The analysis was performed for each of the sections of the circuit as an overall evaluation of the circuit. The Sobol’ method and the correlation method were used to evaluate the Eureka mine concentrator plant using the SimLab 2.2 software."

Jan 1, 2014

By L. O. Filipov, N. E. Menad, A. Geneyton

"Zeta potential of synthetic monazites presenting various compositions were measured to investigate the effect of the main lanthanides substitutions on electrophoretic mobility and resulting IEP. The measurements are performed in a CO2 depleted and enriched solutions showing both reduced influence of monazite chemistry and strong influence of ions resulting from the solubilization and dissociation of CO2. The influence of oleic acid on the electrophoretic mobility of those monazites was also investigated. The influence of pH on oleate adsorption was studied using a bubble/particle adhesion system. Adhesion strength measurements were performed on pure synthetic monazite-(Ce) and monazite-(La). An extensive thermodynamic model of monazite in water was developed to highlight correlations between lanthanides hydroxides/carbonates species concentrations in the bulk solution and oleate adsorption. Based on electrophoretic measurements, advanced thermodynamic consideration and adhesion measurements, further details of the oleate adsorption model on monazite surface were proposed.INTRODUCTION Electrophoretic and potentiometric data on monazite and, a fortiori, other rare earth semi-soluble salts such as bastnaesite are extremely erratic (Chelgani et al. 2015). The isoelectric points measured with electrophoretic mobility methods range from 4.7 to 6.5 although sporadic data indicates an IEP (isoelectric point) far from that range. Different explanations are proposed in the literature to explain the IEP variability notably the numerous chemical substitutions that frequently occurred within monazite crystal lattice (Chelgani et al. 2015). Based on lanthanides speciation diagram, several authors highlighted the influence of specific lanthanide species on the flotation performance of rare earth semi-soluble salts when carboxylate or hydroxamate collectors are used. Although lanthanides ions have a great affinity for carbonates groups (Kragten et Decnop-Weever 1987), lanthanide (hydrogen) carbonates were not implemented in speciation diagrams. In this work, an advanced thermodynamic model is proposed to highlight correlation between flotation performance and lanthanide species predominance but also concentrations. Qualitative measurement of the monazite surface hydrophobicity are performed through tests of adhesion of coarse monazite particles onto bubbles. Since flotation and microflotation technics are highly influenced by hydrodynamic parameters, this method was investigated to obtain a sharp contrast between appropriate and inappropriate pH conditions. This paper is to investigate 1) the effect of lanthanides substitution on monazite surface properties through zeta potential measurements, 2) the mechanism of adsorption of carboxylates on monazite surfaces and 3) the effect of CO2 on monazite surface properties and carboxylates adsorption."

Jan 1, 2018

By Kauko T. Ingerttilä, Jouko O. Kallioinen, Jaakko O. Leppinen, Alexander V. Lashkul, Vladimir E. Nenno

The Separation in Froth (SIF) technique is based on the idea that the pulp is fed directly onto the froth layer prepared on the surface of liquid medium providing an effective method for separation of coarse particles up to a few millimeters size. Thus the SIF process can result in substantial savings in grinding energy and flotation chemicals. In this work flotation of apatite, calcite and silicate minerals from various industrial sources was investigated using laboratory and pilot plant-scale SIF machines. Flotation of diamonds was also investigated on laboratory scale. It was observed that all the minerals mentioned above can be successfully floated up to about 3 mm particle size. Beneficiation tests with the coarse fractions of classification circuits indicated that final grade calcite concentrate can be obtained with over 90% recovery in one SIF step in this grain size (typically 0,1 to 1,5 mm). Similarly, substantial upgrading of coarse apatite was achieved without grinding it to the fineness required by conventional flotation. SIF could also be applied to the recovery of coarse apatite from the tailings of a conventional flotation process. The capacity measured in the pilot plant test runs for a 1 m2 cell was typically 30 t/m2h. Presently, a full-scale process using the SIF technology is being installed for coarse apatite recovery.

Jan 1, 2003

By Rolf Lauten, Yongjun Peng, Yufan Mu

"Biopolymers, produced from cellulosic biomass, have promising prospects of application as depressants in mineral processing. In this study, three different types of biopolymers (i.e., DP-1775, DP-1777 and DP-1778) were used to study the effect of polymer structure on flotation of un-activated pyrite, copper activated pyrite and chalcopyrite. It was found that the depressing effect of DP-1775 and DP-1778 was much stronger than that of DP-1777, and pyrite was depressed to a greater content than chalcopyrite with the same biopolymer at the same dosage. The biopolymer concentration played a vital role in determining the degree of depression. For each biopolymer, the higher the concentration, the greater the minerals were depressed. The mechanism underpinning the depressing effect of these biopolymers was explored in this paper. The concentration of biopolymers could determine the properties of the adsorption layer and the confirmation of biopolymer chains on mineral surfaces. The biopolymer molecules may aggregate when polymer concentration was over a critical value. Molecular weight and functional groups of biopolymers were the key factors characterizing the depressing capability of different biopolymers. Differences between the tested biopolymers and features of the adsorbed layer might account for the observed trends in ability to depress pyrite and chalcopyrite flotation. The greater depressing effect of biopolymers on pyrite over chalcopyrite might result from the preferential adsorption of biopolymers on pyrite over chalcopyrite."

Jan 1, 2014

By Bruno Michaux, Markus Reuter, Martin Rudolph

"It is relatively well-established in the literature that the flotation of calcium minerals using fatty acids as collector is very sensitive to the process water composition. In particular, hard waters have often been reported to strongly reduce the target mineral recoveries due to the formation of insoluble compounds such as calcium and / or magnesium dioleate, thus reducing the amount of collector available for adsorption onto the mineral surface. In this study, the flotation of a fluorite pre-concentrate was performed with tall oil, an industrial collector essentially containing fatty acids. The tests were performed in a variety of synthetic waters to simulate multiple degrees of water hardness, and to differentiate the role of magnesium and calcium ions on the flotation performance. The flotation tests revealed that, under the studied conditions, a significant difference between flotation in calcium-rich and magnesium-rich waters was observed, suggesting strong ion-specific effects in the system. Specifically, calcium-rich waters slightly improved the fluorite recovery, whereas magnesium-rich waters caused a decrease in recovery by as much as 20%. This paper is focused on the flotation kinetics aspect of the system. This approach highlighted the interesting finding that calcium ions did not simply increase the fluorite recovery, but also significantly increased its flotation kinetics. The magnesium ions, on the other hand, had the exact opposite effect.INTRODUCTIONAs the mining industry is facing an increasing number of issues related to its fresh water consumption, the idea of using alternative water sources for mineral beneficiation is gaining significant momentum. As a result, a proper understanding of the role of water chemistry in flotation is becoming more and more urgent, leading to an increasing number of studies on this topic."

Jan 1, 2018

By Rodney J. Hundermark, Sharif Jahanshahi, Shouyi Sun

"The major platinum producers in South Africa make use of electric furnaces for the melting of 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. 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 on Al2O3.CaO.FeOx.MgO.SiO2 slags similar in composition to the melter slags. Conductivity increased significantly with iron oxide content. Above 20wt% FeOx, electronic conduction was significant and the conductivity varied with the oxidation state of the slag. As the iron oxide content was increased further, the electronic mechanism became more dominant. The conductivity reached a maximum at around pO2 = 10-7 to 10-4 atm., although this value was dependent on the total iron oxide content and basicity of the slag."

Jan 1, 2003

By Azin Zangooi, Cesar Gomez, James Finch

Frother concentration is a variable which significantly affects the flotation performance by decreasing bubble size and helping froth stabilization. Variations in frother concentration, which mostly go unnoticed in industrial operations, may affect these functions. Some factors that can cause variations include the fact that frothers are normally dosed based on feed tonnage and not solution concentration, unstable frother delivery, incomplete dissolution for low solubility frothers, addition of frother-free wash water, remnant frother in recycle waters and frother partitioning to the froth. A colorimetric technique developed for determining frother concentration on site makes it possible to detect the occurrence of these problems and to establish their magnitude, allowing conditions to be adjusted to reduce frother concentration variations. By sampling and analysis, frother distribution throughout a circuit can be established, referred to as ‘frother distribution mapping’. Experiences at several concentrators processing sulphide ores are used to illustrate time restrictions for sample analysis, and to demonstrate temporal and spatial frother concentration changes as a consequence of variations in the grinding stage, recycled waters containing frother, and frother partitioning.

Jan 1, 2014

By H. Kasaini

Batch wise adsorption tests for platinum (Pt) on the surface of activated carbon pellets (Norit RO 0.8 BET surface area 1100 mg/g) were carried out in mixed chloride solution. The purpose of this study was to assess and compare the adsorption performance of amine-treated activated carbons (AACs) and native activated carbons (NACs) in terms of adsorption capacity and selectivity. The effect of pH and temperature on adsorption capacity and selectivity was established. The amine- treated ACs were prepared by anchoring the amino groups (butyl amines) on the surface of AC pellets in aqueous media and the UV-Vis was used to determine the amount of amine sequestered from solution by ACs. The dosage of butyl amine on the surface of ACs averaged 0.15 g/g, carbon. The adsorption mechanism was described by the ionization and complexation model whereby interaction between the protonated AAC surface and the anionic chlorocomplex ions (PtCl5 [H2O]-, PtCl62-) proceeded by either electrostatic attraction or/and by covalent bonding [(NH3)2PtCl6 or (CH2COO)2PtCl6]. By comparison, the adsorption capacities of Pt on amine-treated ACs and native ACs were 53.8 mg/g and 33.03 mg/g, respectively which highlight the benefits of anchoring functional molecules on ACs. The selectivity of AACs was influenced by solution pH. Pt adsorbed selectively on the surface of amine-treated ACs at pH<1.5. The highest separation factor that was recoded pertained to Pt and Fe species (ßPt/Fe = 90) then followed by Pt and Ni species (ßPt/Ni = 30) or Pt and Cu species (ßPt/Cu = 15). The lowest separation factor was recorded for Pt and Cr ions (ßPt/N= 5). Adsorption kinetics of Pt on amine-treated AC surfaces, according to the first and second order reactions, were investigated and results showed that rates were in the order 10= 5). -4 min-1 and 102 g?min/mg, respectively. The pseudo 1st order kinetics predicted the adsorption capacity of 51.81 mg/g which was almost similar to the experimental value (53.8 mg/g) while the second order rate equation predicted Pt adsorption capacity of 40.1 mg/g. Both The Langmuir and Toth isotherm fitted the Pt adsorption at pH < 1.0. The Freundlich isotherm tended to underestimate the adsorption capacity of AACs.

Jan 1, 2014