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By C. P. Lowes

"The REFLUX™ Classifier (RC™) consists of a fluidized bed housing, with a system of parallel inclined channels above. This system performs a simultaneous gravity separation and desliming of the feed material, utilising the inclined channels in order to retain the relatively fine dense particles. These particles promote the formation of an autogenous dense medium within the fluidized bed. Relatively large, low density particles are displaced from the fluidized bed and conveyed upwards through the inclined channels reporting to the overflow with other finer particles. Given the hydrodynamic role of both the particle size and density in determining the particle transport through a water based suspension, all gravity separators operate over a limited size range. In the case of the REFLUX™ Classifier, efficient separations can be produced across a very broad size range, from nearly 10 mm down to 10 m, however, for a given application the size range is much more limited. This study was concerned with the processing of dense minerals over a broad size range, and the need for multistage processing. Here the overflow from the first stage cascades to the second stage, incorporating coarse gangue rejection. This approach is shown to deliver remarkably high grades and recovery.INTRODUCTION The performance of the REFLUXTM Classifier (RC™) in beneficiating fine coal is well documented (Galvin, 2012). Although the technology can be applied to relatively fine particles below 0.1 mm, or coarser particles below 2.0 mm or even 8.0 mm (Galvin et al., 2010), in each case the technology is applicable to limited particle size ranges. In coal preparation, the most common size range is 0.25 to 2.0 mm, covering an eight-fold range in the particle diameter. Coal has a relatively low density, typically below 1600 kg/m3, with a significant portion below 1400 kg/m3. In water, the buoyant density difference (~ 400 kg/m3) is therefore low compared to that of gangue minerals (1600 kg/m3) by a factor of 4, enhancing the potential for separation. Thus, in coal preparation, the technology can be applied over a commensurately broader size range, typically up to eight-fold."

Jan 1, 2018

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

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

Jan 1, 2003

By Lev O. Filippov, Inna V. Filippova

"Flotation of metal-organic precipitate in column is sensible to the hydrodynamic conditions determined by the diameter and the dispersion of rising bubbles. Thus, the dissipation energy in the system resulting of ratio between superficial fluid velocities (gas and feed) in the column is the main parameter for precipitate flotation in pilot or industrial scales. The suggested limiting factor is the aggregate stability under the turbulence created by the rising bubbles. The stability of precipitate is related to the structural organisation of aggregates, which determines the size distribution of particles during precipitation and flotation stages.Structural evolution of Mo precipitate and the destruction phenomenon were described by using of the various fractal dimensions. The fractal studies allow the detection of a structural scaled organisation of the precipitate flocs. The fractal dimension of the particle mass distribution Dm=1.94+/-0.15 suggests, for the floc structure, a cluster-cluster aggregation process either with restructuring or breakage phases.The destruction process, which occurs for the lowest values of the dissipation energy E (0.02 . 0.05 W/kg) was characterised by a fractal dimension Dg of size distribution. Besides, the destruction of floc produces very fine particles, and thus induces the difficulties of bubble-particle collision during the precipitate flotation in column."

Jan 1, 2003

By C. Y. Sun

Flotation of chalcopyrite and unactivated malachite with xanthates (ethylxanthate, butylxanthate, octylxanthate and dodecylxanthate) is studied in this paper. Minerals interacted with xanthates are detected by FTIR, and simulated by molecular mechanics. It shows that chalcopyrite can be floated with 4 kinds of xanthates, and unactivated malachite can?t be floated with ethylxanthate but can be floated directly with later 3 kinds of xanthates while characteristic absorption peaks of those four kinds of xanthates are all detected by FTIR on chalcopyrite and malachite surface. After simulating the interaction between xanthate and mineral, it shows that H2O and OH-can interact with chalcopyrite and malachite, and their interaction energy may be so called energy bulwark which must be overcome by collector when collector interacts on minerals; the two sulfur atoms in xanthate group interact with copper and neighbor iron atoms on chalcopyrite. It also shows that molecular mechanics results with logP of collectors can interpret the mechanism of xanthate-mineral on atom scale.

Jan 1, 2014

By Janusz S. Laskowski

It is customary to assume that wettability plays an important role in coal flotation, and it is well established that while hydrophobic metallurgical coals float easily, low-rank less hydrophobic coals are difficult to float. However, coal surface wettability plays a dominant role in many coal preparation unit operations. As it will be discussed in this paper, it affects coal-dewatering, selection of flocculants, fine coal pelletization and briquetting, and even coal handleability.

Sep 1, 2012

By Guanzhou Qui

The utilization status of copper ore resource, the application and development of biohydrometallurgy technology in the world was reviewed. Furthermore, according to the analysis of the characterization of Zambia?s copper resource, biohydrometallurgy technology was shown to be a good way to explore and utilize the enormous low grade copper resource, such as ore tailings and low grade copper ore in this country. Through the cooperation of CSU, China and MMMD, Zambia, ?CNMC-CSU Demonstration Base of Biohydrometallurgy Technology in Zambia? was launched and several biohydrometallurgy plants are being constructed, that indicates the biohdyrometallurgy technology would be applied soon in Zambia and even in the whole Africa. Biohydrometallurgy technology stands as an efficient alternative to the traditional pyrometallurgy process can be the key to unlock mineral resources value. Keywords: biohydrometallurgy, Zambia, copper processing, CNMC-CSU

Sep 1, 2012

By Douglas W. Fuerstenau

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

Sep 1, 2012

By Markus A. Reuter, Albert Scholte, Ewoud V. Verhoef, Gerard P. J. Dijkema

"A dynamic, interactive map has been developed of the life cycle of a number of metals, from mining through to minerals processing, metal production, product manufacturing, recovery and waste management. Whilst the existing metal process network and waste management infrastructure provide substantial scope for (product) design, these also limit change because of the strong path dependency of industry and infrastructure development. The metal production network is complex, as it consists of an interconnected and integrated system that incorporates multiple production routes for a spectrum of metals. More often than not, the production or recovery of a single metal is related to or dependent on the generation or recovery of another. The effects of these other metals is of great importance. In order to realize the potential economic importance of impurities, research and development have integrated the processes of copper production with those of lead and zinc, and connected the processes to those of among others silver, bismuth, tin and platinum group metals (PGMs), for example. The recovery of these elements from the interconnected circuits is extremely complex, as most of the elements must be circulated between two or more circuits before they are concentrated enough to make their extraction possible, and their recovery as a compound profitable.From such a system’s perspective, it can easily be seen that a complication for solid waste management has arisen through the development of products (consumer goods) that bring together metals that are not linked in natural resources. As a consequence, many of these materials are not compatible with any process in the metals production network that was developed for the processing of primary, natural resources, optimized for the processing not only of the primary metal but also for all mineralogically associated minor valuable and harmful elements. The formation of large or complex residue streams or undesired harmful emissions then inhibits processing and recovery of said products at their end-of-life. Another complication is that any change to the system (in metal production, SWM or product design) affects the system configuration. Due to the changing demands for metals as a result from the changing products made from the metals for example, the relationships between the processes in the interconnected metal production systems change. This affects both the demand for old scrap (required amount and grade) from waste management, and the environmental profile of the metals. Preferably, therefore, product designers, waste processors and metal producers must cooperate to realize optimal metal recovery in processing discarded consumer products."

Jan 1, 2003

By Vladimir E. Vigdergauz

"Bubble-mineral complexes could be formatted by an attaching of hydrophobic particles to the surface of air bubbles or by an evolution of bubbles from solution onto hydrophobic surfaces. Measurements of contact angles, detachment forces (DF), induction times (IT), evolution pressures (EP) and flotation recoveries (FR) for the studying of minerals wettability at various pH and electrochemical potentials were used. An analysis of the obtained IT results show that a process of bubble attachment to a mineral surface is a rather slow one and it will scarcely be enough for bubble-mineral complex formation under the conditions of real flotation.The ranges of adhesion potentials obtained by DF measurements, Figure 1, correlate with the data of floatability-potential for pyrite. The ranges of adhesion potentials obtained by DF measurements for galena (-1 ÷0.2V) and chalcocite (-0.5÷1.2V) correlate with the potential ranges of floatability for galena (<0.2V) and chalcocite (>-0.4V). An increase of the DF and the cathodic limit of the adhesion potential with increasing length of the hydrocarbon chain were observed. EP-pH curves for sulfides are a mirror-like to the DF-pH curves, Figure 2. Structure of solid-liquid and liquid-gas borders has a determinative importance for formation of bubble-mineral complexes and subsequently flotation results. Under vacuum on the mineral surface there are produced micro bubbles and preferably they will be appeared on the hydrophobic sites. Water structure breaks near a hydrophobic surface facilitate water mass destruction and formation of gaseous phase embryos under decompression in the impeller zone. It simultaneously reduces a probability of produced micro bubbles dissolution as a result of pressure increasing owing to constant fluctuation of liquid densities into impeller zone. Comparison of Taggart’s evaluation of the suction behind blades of the impeller of an agitation-froth machine and ABEP data on galena, Figure, shows that gas evolution will be observed in the range of 1300-2700 revolutions of impeller per minute for hydrophobic and hydrophilic surfaces successively."

Jan 1, 2003

By Milind Sabne, Pradip, P Kapur, Beena Rai

"The efficiency of an industrial flotation circuit depends on (a) the selectivity and the kinetics of the reagent combination selected for the separation (b) the hydrodynamic conditions prevailing in the flotation cell (essentially equipment design parameters) affecting both the pulp and froth phase (c) the operating parameters such as feed rate, pulp density, pH, temperature etc. including the mineralogy, particle size distribution and relative proportion of liberated and composite particles of constituent minerals in the feed to flotation circuit and (d) the circuit configuration itself. We have developed a molecular modelling based reagent design and selection framework to assist mineral engineers to arrive at the preferred reagent combination based on a rigorous, scientific and quantitative comparison of various options available for this purpose. Similarly we have also utilized a general circuit design methodology proposed by Kapur and Mehrotra in 1974. The advances thus made in modelling both the reagent chemistry as well as circuit design, along with the availability of sophisticated, automated tools for characterization of ores (liberation as well as mineralogical composition of the different flotation streams) provides a scientifically rigorous, quantitative, robust framework for design and optimization of complex flotation circuits. We illustrate in this paper the power and the utility of our rigorous optimization based approach to designing industrial flotation circuits for the beneficiation of a multi-component feed with the help of few case studies from our own work. With the proposed methodology, higher levels of process efficiencies can be achieved in the industrial flotation plants, in particular those processing complex, multi-component feeds requiring multiple stages of flotation separation. We are currently developing an IT platform consisting of computer-aided decision support tools for arriving at the preferred flotation circuit and the appropriate reagent chemistry for a given ore deposit and/or a given plant."

Jan 1, 2014

By Bronwynne K. Williams

"In deriving flotation kinetic models, the froth phase was, until recently, either ignored or treated entirely empirically. The behaviour of the froth is now known to be usually important and sometimes dominant in determining flotation performance. Hence numerous methods have been developed for sampling the flotation froths and models incorporating the effects of the froth behaviour have been derived.Such models will assist in determining more accurate estimations of the kinetic parameters utilised in the designing of industrial scale plants thus reducing the incurred costs of over designing. In particular, improved models for batch tests may lead to more effective use of batch testwork for prediction of continuous plant behaviour. A more detailed model is thus proposed which allows for a more realistic approach to the flow distribution in the froth phase.PROPOSED MODELThe batch flotation process is split into two stages in time, namely before the froth begins to overflow and after. The assumptions made, and hence the calculations, are different for each stage.The air enters the slurry at t=0 and generates froth. The superficial velocity of the air through the cell is given by go. It is assumed that the rate of froth breakage (gb) is constant during the first stage. The froth rises with a uniform net velocity throughout the cell and no mixing is assumed to occur.After the froth begins to overflow, the velocity distribution of the gas is modeled by segmenting the froth phase as shown in Figure 1. A model for bubble breakage rate or measurements of froth velocity allows one to obtain the volumetric rate of concentrate froth production. The entrained water and associated particles and a drop-back mechanism are also allowed for in the model."

Jan 1, 2003

By M. Evertsson, E. Hulthén

"In aggregate production and mining the operators are responsible for controlling and monitoring the process to maintain high plant throughput and safe operation. Operators have to make different decisions to control the process due to changed demand on the operation from both management and conditions of the process. The quality of the response and the time it takes for an operator to respond to altered demand relies on what information is available and the experience of the operator. In this work a dynamic simulation platform has been developed to be used for operator training. Models for representing production units and process control for plant simulations have been developed and implemented in MATLAB/SIMULINK to simulate time-dependent plant behavior. Stochastic and scheduled events are included using the discrete events simulation toolbox SimEvents. The human-machine interface was developed using the human-machine interface software ICONICS. The operators’ cognitive process, in interpreting the plants semantic, has been studied by observations and with informal interviews with operators. This was done to get information about the daily operation and the problems that occur in the process. By interacting with operators that experience different physical interactions with the process; more qualitative e-learning software for supporting operator training in a dynamic operator environment could be developed. The quality of the operator training environment was evaluated with a usability study that was performed with operators and others within the production."

Jan 1, 2014

By J. D. Miller, C. L. Lin

In general, x-ray computed tomographic (CT) techniques are able to provide 3D images of the internal structure of opaque materials in a nondestructive manner. The unique cone beam geometry allows acquisition of all 2D projections with only one rotation of the sample thus providing for fast data acquisition and better x-ray utilization, as a complete 2-D detector array receives the cone-shaped flux of rays. Thus, an isotropic 3D volume can be reconstructed without the mechanical translation and the stacking of sequential slices as is the case for more conventional CT scanners. In this regard, a state-of-theart, custom designed x-ray microtomography facility to provide very detailed 3D spatial analysis of multiphase particles has been installed and is in operation at the University of Utah. The reconstructed 3D tomographic volume allows for an adjustable spatial resolution from 5 to 20 microns for sample dimensions from 10 to 40 mm in diameter, respectively. For example, a packed bed of coal particles is shown below in which different crystalline froms of pyrite are distinguished in 3D.

Jan 1, 2003

"The thiosulfate leaching process developed by Barrick to treat sulfidic high preg-robbing gold ores uses calcium thiosulfate as the leaching reagent for ores pre-treated by pressure oxidation, resin for gold recovery with sulfite/trithionate elution and reverse osmosis as a means of reagent recovery. A large portion of the research that led to the development of the technology was based on previous studies completed by different groups over the years, mainly focused on the ammonium thiosulfate system. Operational limitations in the use of the ammonia-containing recycled water in the pressure oxidation circuit were some of the main drivers for the change from ammonium to calcium thiosulfate for the development of the industrial scale process. One of the main aspects for successful gold extraction and recovery in the thiosulfate system is the pseudo-equilibrium reactions that drive distribution of the different gold species (in solids, solution and on resin) in the system. Previous studies have been focused on the thiosulfate reactions and equilibrium constants for the oxysulfur ions (thiosulfate, trithionate, tetrathionate). However, the literature around the effects of the different metal-oxysulfur complexes (Cu and Hg complexes) that form when the ore is in contact with the leaching reagents, and the related effects on stability of the gold complex is limited. The main changes in the gold complex chemistry and stability in the calcium thiosulfate system as compared to the ammonium and sodium equivalents, as well as related effects on gold recoveries, were investigated in the presence of different types of double refractory ores. INTRODUCTION Barrick has developed a thiosulfate leaching process to treat double refractory gold ores, by combining the use of acidic and alkaline autoclave pre-treatment with thiosulfate resin-in-leach (RIL). The process currently in operation at the Goldstrike mine (the TCM process), uses calcium thiosulfate as the leaching reagent, resin for gold recovery with sulfite/trithionate elution and reverse osmosis as a mean of reagent recycle. The main feed to the process plant is highly preg-robbing sulfidic ore from Goldstrike’s open pit. Prior to feeding the pressure oxidation circuit, the ore is processed through the crushing and grinding circuits and treated in preparation for acid or alkaline autoclave processing (POX)."

Jan 1, 2018

By Sonia Helle, Ursula E. D. Kelm

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

Jan 1, 2003

By Igor P. Solozhenkin, Peter M. Solozhenkin, Sanda Krausz

"In this work, authors will show the efficiency of computer technology and chemical programs at studying collectors for flotation of minerals of elements of platinum group (EPG). Clusters various minerals EPG (flotation reagents) are created, named us clusters minerals (reagents) as their structure corresponds to the chemical formula, and the distance between separate atoms corresponds to the known tabulated data. By molecular modeling are investigated clusters sperrylite PtAs2, stumpfilyte PtSb, sadberryte PdSb, sobolevskite PdBi, palladoarsenyte Pd2As, paolovyte Pd2Sn, rustenburgyte (Pt3Sn, Pt6Sn2) and their computer parameters (absolute rigidity, electronegativity, transfer factors of carry, charges of the atoms) are determined. Tellurides of palladium (IV, II) merenskyite PdTl2 and kotulskyte PdTe and platinum clusters are investigated: PtFe4, Pt3Fe, PtFe (Pt2Fe2), Pt2Fe (Cu) Ni. The technique of attachment of the collector (composites) to cluster atoms EPG is offered. For the first time, it is established that at linkage of flotation collectors on monodentate, bidentate and bridged to circuits with atoms clusters the minerals containing atoms As, Sb, Bi, Pb, Sn, reaction of connection with change of a degree of oxidation of these atoms and occurrence of a proton operates. It is executed virtual skirling organic compounds connections by the developed criteria from accessible libraries of a database. The principle of an estimation of interaction energy for flotation reagents with mineral clusters is offered. It is developed the prognosis of collector activity evaluation (P?AE) and his values for candidates in collectors for flotation of minerals EPG are calculated. For flotation of ores containing Pt and Pd minerals, a number of reagents, including compounds on basis P (III), for innovational technology of Pt, Pd mineral flotation are recommended. Key words: flotation, minerals, flotation reagents on the basis of phosphorus (III), molecular modelling, chemical programs, program ????? , electronic energy."

Jan 1, 2014

By Isaak I. Maksimov, Tatyana E. Koltunova, Mikhail F. Yemelyanov, Liudmila A. Otrozhdyonnova

"INTRODUCTIONMetals losses amount up to 50% in coarse fractions in (>100 µm) and composite particles, and to 20- 25% in fine fractions (<10 µm) at non-ferrous floatation concentrating plants of the CIS. Therefore, reduction of metals losses in difficult fractions is of high significance.IMPROVEMENT OF FLOATABILITY OF COARSE AND COMPOSITE PARTICLESReagent regimes with application of strong collectors – xanthates ?5-?8, combination of butyl xanthates and aerofloats ?10-?12, butyl xanthates with hydrocarbons are proposed for this purpose. Application of such reagent regimes for copper and copper-molybdenum ores permitted to increase copper and molybdenum recovery by 0.5-3.9%.Studies, performed by means of specially designed non-frothing flotation machine with independently controlled agitation intensity and narrow size-ranges of air bubbles, established that the best results are achieved with employment of bubbles of 0.5-0.8 mm size regarding particles of any size, with small amounts of up to 2 mm size “transport” bubbles to be expediently used for floatation of coarse particles.Energy dissipation in the main volume of floatation cells must be lower than 0.2-0.25 m2/s3.Performed experiments permitted to formulate requirements to development of machine for floatation of coarse and composite particles. Such floatation machine with volume of 8.5 m3 provided for weak agitation in the main volume of floatation cell and uniform distribution of coarse particles throughout the depth owing to establishing of pulp circulation with upward flows. In addition, in the upper part of floatation cell where agitation is considerably weaker, favorable conditions are created for attachment of particles to bubbles. Testing of this floatation machine demonstrated a 7.5% increase in recovery of +0.2 mm particles in pyrite floatation and a 12-14% increase in recovery of +0.2 mm particles in apatite floatation as compared with a reference floatation machine."

Jan 1, 2003

By H. Lieberwirth, M. Hesse

"Selective comminution (SC) is beneficial for the treatment of primary raw materials, especially if it is utilized in the pre-concentration process. Pre-concentration processes are applied in mineral processing to relieve subsequent processes and to achieve a higher efficiency. SC is also a promising method for the treatment of low-grade ores and waste dumps. With SC, various components can be separated such as valuable minerals from waste, ore from wall rock and different ore varieties within a deposit. SC is a property of a comminution system and leads either to a preferred crack propagation in one component (called preferential breakage) or to a preferred crack propagation along the grain boundaries (called interfacial breakage). SC results from different comminution behavior of various components in the feed material. For mechanical comminution, the preferential breakage seems to be the most important case of SC. Hereby SC generates only the difference in the particle size which can finally be used as a sorting parameter. A sorting process which uses SC depends on three parts: the feed material, the comminution machine and the separation machine. The feed material defines the potential for SC. Differences in properties like strength, toughness and density which are related to comminution are often used. The comminution machine has to exploit this potential. The extent of the exploitation can be influenced by the machine design, material and operational parameters. After SC, the various components are still combined in the product. So ultimately, a separation machine is needed. At preferential breakage, a simple screening machine can be used. The basics about SC will be presented at first. This contains relationships between material properties, the kind of loading in the comminution machine and the SC effect. These basics can be used for example to exploit a potential to SC for a pre-concentration step or to avoid the SC for a higher efficiency of subsequent processes. Based on recent investigations with impact load, the influence of the important parameters compressive strength, density, particle size and impact velocity to the SC will be shown, using examples of lead-zinc ore comminution and fluorspar processing."

Jan 1, 2018

By Lev O. Filippov, Inna V. Filippova

"Flotation of metal-organic precipitate in column is sensible to the hydrodynamic conditions determined by the diameter and dispersion of rising bubbles. Thus, the dissipation energy in the system resulting of ratio between superficial fluid velocities (gas and feed) in the column is main parameter for precipitate flotation in pilot or industrial scales. The knowledge of aggregate structure can lead to better understanding and control of many solid-liquid separation processes (sedimentation, filtration, thickening and flotation). Many authors highlight the importance of structural properties (i.e. floc density) for different industrial applications.This approach was applied to achieve the flotation of molybdenum precipitate obtained with organic collector a- benzoin oxime for molar ratio 1:2. Flotation tests were carried out at lab and pilot scale with rigorous control of the size distribution of bubbles and the values of dissipation energy in the systems.Structural evolution of Mo precipitate and the destruction phenomenon were described by using of the various fractal dimensions, which were deduced from experimental data of laser sizer devices and optic microscopy pictures of precipitate. The boundary fractal dimensions Df of large aggregates allows the detection of a structural scaled organisation of the precipitate flocs (elementary germs-microflocs-flocs). The fractal dimension of the particle mass distribution Dm=1.94+/-0.15 suggests, for the floc structure, a cluster-cluster aggregation process either with structuration or breakage phases.The destruction process characterised by a fractal dimension Dg controls the final size distribution. The floc destruction occurs for the lowest values of the dissipation energy (0.02 – 0.05 W/kg). The relation between Dg and the system dissipation energy Et (for various energy E dissipated in the agitation cell) involves the different breakage mechanisms of aggregates in function of the aggregation bonds (Fig. 1).Besides, the destruction of floc produces very fine particles (elementary germs or/and microfloc according to E), and thus induces the difficulties of bubble-particle attachment during the precipitate flotation in column. Yet, very small bubbles, which increase the collision probability, would make the flotation feed rate decrease. The optima ratio between superficial gas and feed velocities are determined for bubble size and flotation results control at pilot scale. Thus, it is possible to providing the catastrophically changes of precipitate column flotation by using the following established experimental relation: the mean diameter d of the flocs under the action of dissipated energy Et follows a power like law (d~Et -0.5). This allows estimating the size distribution of flocs for the E values which can appear in column."

Jan 1, 2003

By Heinrich Hutchison, Thomas von Moltke, Roelof F. Sandenbergh, Katarina P. Cerovic

Although the cyanidation process for gold leaching has been applied for more than a hundred years, some aspects of it, such as the passivation of the gold and the depassivating action of heavy metals, are still not well understood. In this work the anodic behaviour and surface composition of gold in alkaline aqueous cyanide with lead additions were investigated using polarization experiments and XPS. It was found that lead in the solution activated the gold at low concentrations, somewhat more positive than the reversible potential for gold, but that the activity again decreased at higher concentrations of lead. The potential range for the activation of the gold coincides with that where underpotential deposition of lead occurs, i.e. –200 to –600 mV(SCE), as indicated by the surface composition of the gold, shown in figure 1. Note that the concentration of lead on the surface of the gold only increased with time in the bulk plating potential range for lead, where gold is not activated by the presence of lead. It is also shown that up to 20 mg/L of lead added to the solution will activate the gold, provided that bulk plating of the lead is avoided. It is also important to avoid reducing conditions during leaching, where bulk plating of lead may occur, if the gold is to be activated by lead to achieve a high leaching rate, as the bulk plated lead screens the surface rather than activating it.

Jan 1, 2003