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By Zoran M. Stevic, Mirjana M. Rajcic-Vujasinovic, Zvonimir D. Stankovic

"Covellite is one of the most important copper sulfide minerals. Its behavior during the anodic polarization, as well as its rest potential in various solutions are of importance for flotation processes and also define the mechanism of electrochemical extraction of copper from sulfide minerals.Measurements of the rest potential have been performed in water solutions in presence of different cations and anions. The existence of the Nernst type dependence of the rest potential on the activity of some of the investigated ions was established. The biggest influence on the rest potential of covellite exhibits the change of activities of the ions forming the crystal lattice of investigated mineral, i.e. Cu(II) and S(II). The dependence of the rest potential of covellite on logarithm of Cu(II) activity has a shape of a strait line with a positive slope of 60 mV, while when concentration of S(II) anions increases ten times, the rest potential of covellite decreases about 120 mV. The first dependence was established in acid medium, while the second was registered in alkali one.Different electrochemical techniques have been used for the investigation of the behavior of covellite during anodic polarization. In the basis of all these measurements is a three electrode system consisted of: 1) working electrode made of the sample of natural covellite from the Bor mine (Eastern Serbia, Yugoslavia); 2) reference electrode (saturated calomel electrode) and 3) counter electrode (flat platinum). Electrolyte solutions used in these investigations are of the same kind as those used in the rest potential measurements. Sulfate and chloride solutions, as well as the mixed sulfate/chloride solutions, are the most perspective from the application point of view.Cyclic voltammetry has been the first used method that confirmed the formation of passive layer on the electrode surface during anodic polarization. Elementary data about the reaction mechanism have been obtained too. More detailed data needed for more precise conclusions about the mechanism and rate of the anodic process on covellite have been obtained by galvanostatic method. It was established that the essential difference exists between the reaction mechanism in sulfate and chloride solutions. Also, the difference is exhibited in the nature of reaction product directly connected with the passivation of the electrode surface. Chronopotentiometric investigations have been performed in sulfate, nitrate, chloride perchlorate and mixed sulfate/chloride solutions applying different current densities. The shape of obtained curves indicate if there was a surface passivation and how intensive it was."

Jan 1, 2003

By J. Vilcáez

The copper extraction yield from thermophilic bioleaching of chalcopyrite depends on temperature, pH, and the oxidation-reduction potential (ORP), as well as the activity of the microbe used. We studied copper extraction yields obtained from chalcopyrite with three thermophiles, Acidianus brierleyi, Sulfolobus metallicus, and Metallosphaera sedula, under various pH and temperature conditions and with different initial amounts of ferric iron. The results indicated that the capacity of each thermophile strain to leach iron as Fe3+ differed, which affected the influence of pH, temperature, ORP, and microbial activity level on the yield of copper. Microbial activity can cause ORP to be close to the critical value (450 mV) at which copper extraction at 65 °C can be higher than that at 80°C. An initial pH of 1.5 retards the precipitation of jarosite, allowing temperatures as high as 80°C to result in copper extraction yields close to 100%. However, if a thermophile with a poor capacity to form Fe3+ is employed, 100% copper extractions can also be obtained at pH 2.5, because ORP is low as result of low amounts of Fe3+ in solution. Optimum temperatures for the growth of thermophiles did not always mean high copper extraction yields. Conversely, high biomass concentrations depending on the capacity of the thermophile strain to leach iron as Fe3+, can result in excess Fe3+ in solution, leading to the precipitation of large amounts of Fe3+ as jarosite. The bioleaching capacity of A. brierleyi was reduced or suppressed when insufficient initial Fe3+ was pro-vided to trigger the leaching reaction, whereas S. metallicus and M. sedula were less sensitive to the initial availability of Fe3+. This result confirmed that a direct enzymatic attack on the mineral surface could initiate the leaching reaction, but later ORP governed the leaching rate of chalcopyrite.

Jan 1, 2014

By Barbara Peszko, Tadeusz Tumidajski

"Various methods are used to identify the grain composition of fine-grained materials because so far the best notion of the grain size has not found and there is no single method to define grain size. In practice the most important are the following grain sizes: sieve diameter dt, effective diameter de, substitute diameter d2 and statistical diameter dst. The mentioned sizes are connected with the methods of analyses. Methods are correct but measure of different diameters of grain and their results are different.The most important methods of granulometric composition analyses are the following: the sieve analysis, the sedimentation method and the conductometric (Coulter-Counter) methods. In each of these methods various physical features connected with the grain size are measured.Sizes of grains defined by different formulas or measurement methods are associated mutually by dependencies, which are results of differences in their determination or calculation ways.In order to determine principles of results comparison the classification analysis results on linearly or non-linearly connected was made. Analyses which results demonstrate the same type of grain size distribution are treated as linearly connected. It is based on the general formulae which determines the probability density function of random variable which is the function of another random variable having the known density function.In order to show the difference in the grain composition of the same material qualified by different methods, three methods of investigations were distinguished. They are: the sieve analysis performed on precise sieves, the sedimentation analysis performed by means of a sedimentation balance “Sartorius” and the microscopic analysis performed after preparing a microscopic slide where the grain size was measured by the Martin’s method.The materials selected for the analysis were quartzite and glass, which are the material of high purity.The obtained results of mentioned above three types of analyses were approximated by distribution function of four distributions: Weibull, log-normal, cut Weibull and Gaudin-Schuhman."

Jan 1, 2003

By Alim Gül, Güven Önal

"Recently, there have been some attemps on the treatment of low grade ores and old plant tailings due to the decrease in high grade ores and the increase in the metal consumption with increasing world population. Cost of mining and beneficiation of low grade ores become prohibitive since the costs of grinding before flotation make the process unfeasable. Therefore, preconcentration of these ores prior to flotation becomes more important. The concentration of ores preconcentrated in coarse sizes provides a decrease in investment costs as well as grinding and flotation costs. Additionally, the requirements of less space for tailing disposal and less reagent consumption are also important from the viewpoint of environmental considerations.In this study, ore sample containing 0.6 % Cu and taken from Küre-Asiköy ore body was used. Ores contained chalcopyrite and pyrite as main minerals and diabaz, quartz, chlorite and sericite as gang minerals.Samples were all crushed under 9 mm by considering the preliminary studies and float and sink experiments were carried out with the sample in the size range of –9+1 mm using different densities of heavy liquids. As a result of these tests, it was shown that 60 % of the material should be discarded as tailings with 0.1 % Cu content. By considering float and sink test results, the following experiments were performed by using heavy medium cyclone and jigs.As a result of heavy medium cyclone tests, which are conducted on the sample in size range of –9+1 mm, 57 % of the feed material was discarded as tailing with 0.08 % Cu content and 7 % Cu loss, while a concentrate containing 1.43 % Cu was produced with 93 % efficiency (Table 1). Jig tests were done with the samples in the size range. As a result of jig tests with –9+1 mm size group sample, approximately 46 % of feed material was discarded as tailings with 0.13 % Cu content and 10.6 % Cu loss, while a concentrate with 0.94 % Cu content was obtained (Table 2)."

Jan 1, 2003

By Masakazu Niinae, Tasuma Suzuki, Mai Moribe, Yohhei Okabe

Bench-scale electrokinetic experiments were performed to elucidate the electrokinetic remediation mechanisms of arsenate from artificially contaminated kaolinite. The electrokinetic experiments in which a constant voltage was applied demonstrated that high soil pH favored arsenate remediation with respect to both the remediation time and electricity consumption. It was also demonstrated that applying a pulse voltage (1 hour ON, 1 hour OFF) significantly improved the electricity consumption efficiency when the soil pH was maintained at the initial value during the experiments; this trend was not observed when the soil pH was gradually increased from the cathode side. These electrokinetic experimental results indicate that the remediation rate-limiting step varied with soil pH. When the soil pH was maintained at the initial value of 7.2 during the experiments, arsenate desorption was the remediation rate-limiting step rather than the migration of dissolved arsenate toward the anode. Conversely, when the cathode pH was not controlled and the soil pH was correspondingly increased gradually from the cathode side, the migration of hydroxyl and desorbed arsenate ions toward the anode played a more important role in the control of the overall remediation efficiency.

Jan 1, 2014

By S. F. Kaplan, A. S. Dolotov, V. N. Kovalev

"At this point in time, autoclave recovery (POX) followed by sorption cyanidation (CIL) is one of the most promising technologies for the efficient processing of refractory and double refractory gold-bearing sulphide rock. This hydrometallurgical technology requires the use of a large amount of water (up to 5 tons per ton of used concentrate), resulting in highly saline water with high pH (pH 9-11), high content of cyanides (up to 300 mg/l), arsenic compounds, antimony and a number of heavy metals. In order to determine the possibility of using recycling industrial water in POX-CIL technology, several batches of experiments were conducted (using the double refractory flotation concentrate of the Mayskoye deposit). Urban water with a chloride ion content of 10 mg/l was used during the reference POX-CIL experiment as the liquid phase of the ??? feed pulp. At that, gold extraction rate amounted to 89.4 %. A full cycle of POX(200 ºC)-CIL was carried out during the first part of the experiments; at that, fresh concentrate of the untreated recycling water with cyanide ion content of 95.4 mg/l, left after the completion of the previous CIL cycle, was used for repulping. It has been established that direct use of untreated recycling industrial water is impossible due to a sharp decline in gold extraction (preg-robbing) down to 79.5%. The presence of chloride ions, cyanide ions and other ligands in the liquid phase provides effective complexion formation for the recovery gold; complex gold compounds are quickly and firmly sorbed by the natural carbonaceous substances of the concentrate at the stage of autoclave recovery; they are virtually not cyanized onwards, and gold is carried over to the tailings. During the the second batch of experiments, recycling industrial water with cyanide and chloride ions' concentration of 500 mg/l each was subjected to the reverse osmosis desalination (up to 6 times in a successive order). After each desalting cycle, such water was used as the liquid phase of the feed pulp in POX-CIL. 6 cycles of RO desalination enabled the extraction of 86.1% Au (which is close to reference recovery). During the third batch of experiments, recycling industrial water was diluted with distilled water (2, 4, 16, 32, 64 times); after each dilution cycle, this water was used as the liquid phase of the POX-CIL feed pulp. Gold extraction after 64-fold dilution amounted to 82.6%. The results of the conducted researches show that the use of untreated recycling industrial water in POX-CIL hydrometallurgical technology is absolutely impossible due to a sharp decline in gold extraction. Even the 64-fold dilution with pure water is inefficient both from the perspective of gold extraction and of rational use of water. Reverse osmosis desalination solves the problem of water treatment except for the removal of cyanide ion, which requires separate reagent treatment of water."

Jan 1, 2018

By A. D. Shuloyakov, G. A. Finkelstein, V. I. Kurets, A. K. Vedin

"In disintegrating solid ores with mineral values disseminated in them, one of the principal tasks is to selectively separate valuable mineral particles from the matrix in which they reside, striving at the same time to keep their natural shape and size as intact as possible.The conventional mechanical disintegration methods do not meet this most important requirement in full. The other major objective here is to reduce electric power consumption during the fragmentation stage, since up to 65 per cent of the total power consumption at concentrators processing ores of non-ferrous, ferrous, rare, and precious metals is spent on disintegration steps.Numerous experiments conducted on dozens of ore types (tin, tungsten, and many others, as well as on rock containing diamonds, rubies, emeralds, etc.) have invariably demonstrated by far superior integrity of mineral values as compared with that obtained by mechanical as well as other types of disintegration.However, the process remains as power-intensive as ever which is due to the imperfect nature of the electro-technical devices that convert the network electric current into high-voltage electric impulses responsible for the disintegration process.The maximum capacity attained in disintegrating the hardest materials from 40 mm to 2 mm size in a single operating chamber with four high-voltage electrodes does not exceed 1.0-1.5 t/h. Attempts at increasing the number of electrodes and the capacity of the operating chamber have failed so far because of high overall dimensions and mass of the electrical part of the installation supplying the chamber with pulsating current, as well as of the commutation requirements. At the same time, a number of overseas operations have reported a significant breakthrough in their attempts to reduce dozens of times the overall dimensions and mass of the discharge impulse generating installation (EIS), which enables us to contemplate to increase the capacity of the EIS at least ten times in the nearest future. Yet, even with the currently achieved capacity of the EIS, these installations have found wide use in geological surveying, precious and semi-precious stones production, in grinding super hard materials, etc., since they provide spectacular selectivity of disintegration and thus the integrity of valuable mineral crystals."

Jan 1, 2003

By A. N. Zagorodnyaya, T. N. Bukurov, Z. S. Abisheva, A. S. Sharipova

"This work presents the results of the development of a flowchart for the processing of copper production dusts resulting in the production of of lead sulphate, tribasic lead sulfate (TBLS), ammonium perrhenate, zinc, copper-cadmium cake.Dust having the following composition (wt. %): Pb 39.3, Zn 6.5, Cu 5.5, Stotal 10.8, As 1.05, SiO2 0.6, Cd 0.8, Bi 0.04, Ag 0.02, Re 0.03 was used in the work. Chemical and X-ray analyses indicated that lead, zinc and copper are generally present in dusts in the form of sulfates, various amounts of oxides, sulfides, silicates; sulfur (according to chemical analysis data) is present in the form of sulfates (~ 90%) and in the form of sulfides (~ 10%).Studies have been made on two-stage stripping of copper production dusts containing lead, zinc, copper, cadmium, rhenium in the form of various compounds, at first with soda solution, then with nitric acid solution. It has been indicated that the combination of the operations allows the recovery of 98% rhenium, 82% lead, 92% copper, and 96% zinc and cadmium each in the solution. Furthermore, at the stage of dust leaching with soda, 80% of rhenium and 0.01% of nonferrous metals each are recovered in the solution. Remaining quantities of all metals are recovered in nitric acid solution up to maximum values. Such behaviour of metals is caused by metal phase content in dusts and properties being formed during leaching of compounds. At the stage of dust leaching with soda solutions, carbonates with various compositions are formed due to the exchange reaction between nonferrous metal sulfates and sodium carbonate. The conversion of PbSO4 into PbCO3 is apparently occurs in the solid phase and the conversion of readily watersoluble zinc, copper, and cadmium sulfates into that of carbonate salts occurs in the liquid phase. Rhenium passes into solution due to the presence of rhenium greater quantity in dust in the form of readily soluble perrhenate. Some portion of the perrhenate is, probable, blocked by lead sulfate and liberated in the conversion of PbSO4 into PbCO3."

Jan 1, 2003

By Williams Calderon, César Arredondo, Gonzalo Montes-Atenas

The quality of final concentrate in froth flotation circuits is largely dictated by the correct implementation of the froth washing operation in flotation cleaning stages, which are commonly installed in column flotation cells. In flotation plants, this aspect has been largely overlooked and the froth washing is restricted to the use of perforated piping through which process water flows producing a similar effect to that observed in "fountains": jet created with low energy crosses the froth phase washing out entrained particles as well as particles weakly attached to bubbles. The aim of this research study is to assess the efficiency of traditional froth washing systems theoretically and experimentally. A theoretical model was implemented using Fluent® software where a jet of variable speed was introduced in a continuous soft matter phase with physical properties similar to those observed in a froth phase in wet and dry conditions. In addition, a simple experimental protocol was designed to validate the model. It was found that the water process jet-like flow influences the behavior of 2 to 3 times the equivalent volume in the froth phase. Such influence zone is dramatically reduced as the froth phase becomes drier. These results were confirmed by the experimental findings indicating that a better froth washing technologies must be assessed and implemented. Some aspects of the ideal froth washing system are derived and discussed in details.

Jan 1, 2014

By P. Hatefi, O. Rahmani, M. Noor-Mohammadi, A. Tohry

"Depressants play an important role in the selective separation of impurities from iron minerals by direct or inverse flotation. In this paper, sodium co-silicate (SCS) with chemical formula of Na4SiCO6, as a depressant with pH modifier features, has been synthesized and used for phosphorus bearing iron ore in anionic reverse flotation. In this process, phosphorus is floated while the iron oxides are depressed, using fatty acids as collector in an alkaline medium. Batch and pilot flotation tests were carried out to investigate the influence of SCS on the separation selectivity of phosphorus from iron oxides. Also the depression mechanism of SCS on hematite surface was investigated by microflotation tests and FTIR spectroscopy measurements. The flotation results indicated that without using a pH modifier, the pH of pulp could reach up to 10, when SCS was used as depressant. In this condition, a better depression performance was observed compared to sodium silicate (SS). Using the SCS, phosphorus and total iron content in iron concentrate was 0.046% and 66.29%, respectively, compared to SS where these values were 0.06% and 65.75%, respectively. As a result the weight recovery of iron concentrate was increase by around 4%, compare to SS. It was also found that 238 g/t of SCS could be used instead of 3 types of reagents collectively, including 32 g/t of NaOH, 151 g/t of Na2CO3 and 400 g/t of SS gel.INTRODUCTIONThe phosphorous presents in iron ore minerals is mainly in the form apatite mineral. The apatite is separated from iron ore minerals by magnetic and flotation methods (Ma, 2012). The reverse anionic flotation of iron is one of the most common method for removing phosphorus from iron concentrate (Araujo et al., 2005).Usually apatite minerals are readily floated using anionic collectors such as fatty acids (Ma, 2012). In this conditions the iron minerals are depressed and by modifying the pH in alkaline conditions, selective separation of phosphorus from iron concentrate can be achieved. Depressants including; sodium silicate (SS), starch, dextrin, guar gum and humic acids play an important role in the reverse flotation of iron ore (Kar et al., 2013; Ma, 2012; Turrer and Peres, 2010; Araujo et al., 2005). Studies have shown that SS has a better effect on iron recovery and phosphorous reduction, compared with other depressants (Tohry and Dehghani, 2016; Qi et al., 1992, Dho and Iwasaki, 1990). In most flotation processes, modifiers are used to adjust the pH. To achieve alkaline conditions, mainly pH modifiers such as carbon dioxide and sodium carbonate are used."

Jan 1, 2018

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

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

Jan 1, 2003

By Braulio Fernández, Gonzalo Montes-Atenas

The mechanisms taking place during the leaching of chalcopyrite when it is in contact with other sulphide minerals, particularly pyrite, is still a matter not fully solved. The GalvanoxTM process has been suggested as a technical solution to extract copper from chalcopyrite at commercial level inhibiting passivation phenomena widely reported in the field of hydrometallurgy. Although there are some rules of thumb to implement the process in fully flooded stirred conditions such as the optimum pyrite/chalcopyrite mass ratio should range between 2 and 4, among others; not many research studies have been focused on studying the effect of the surface contact area between chalcopyrite and pyrite to reach best copper extraction conditions. The aim of this research work is to determine the effect of the mass and surface area ratio between the minerals and the surface area of each of the mineral species effectively exposed to the leaching solution. Different particle size distributions of pure pyrite and chalcopyrite were contacted in a small column and subjected to leach tests using sulphuric acid in concentrations close those used in industrial leaching processes. The mass and surface area ratios which optimize the extraction of copper were obtained. It was found the best leaching conditions were attained when reducing the particle size distribution of pyrite regardless the particle size distribution of chalcopyrite. Further analysis concerning the impact of this conclusions on large scale operations is presented and discussed.

Jan 1, 2014

By Rodrigo Ladrón, Gonzalo Rund, Gonzalo Montes-Atenas

Modelling ore comminution processes have been a highly fruitful scientific topic. The models have been proved to be largely dependent on the selected comminution technology. Among them, semiautogenous (SAG) mill technology has been widespread implemented in plants but no complete understanding of the mechanisms involved in the process is available. Tracing back in history, SAG models considered only some granulometric cut sizes such as the t10 and attempted to relate these parameters with the energy involved in the impact between particles. Other models evolved towards incorporating physical properties of the material being ground and the mill operating conditions. These material properties have assisted to obtain a more comprehensive description of the breakage mechanisms; nevertheless, the gathering of all known parameters still have not delivered a model able to describe the process. This may be a result of emergent properties or phenomena originated from interactions inside the process which are hard to predict turning the size reduction operation into a complex system. Cellular automata provide one answer to describe complex systems by following simple rules. The aim of this research work is to establish the preliminary rules of thumbs enabling the implementation of cellular automata able to predict the particle size distribution at the exit of a SAG mill. The methodology involved developing a simple 2D model of a ROM sample. Plant data from two mine sites were correctly described by a set of three rules: two rules describing the particle reduction and one rule associated with material transport across the mill. Further analysis related with expanding this model to 3D and its impact on the liberation of valuable material is also discussed.

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 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 David I. Verrelli, Peter T. L. Koh

"Recent experimental measurements of induction time made by direct observation with the ‘Milli-Timer’ indicated that angular particles were able to attach much more rapidly than spherical particles. There was around a tenfold difference in the respective induction periods for particle-bubble attachment. For industrial application, a more holistic comparison is needed, with the induction period for attachment being just one input. Over the years, CSIRO has developed a CFD-flotation model that incorporates both rigorous hydrodynamics, to simulate real industrial cell geometries, and a detailed model of the embedded flotation process, in which the induction period is an important parameter. We conducted transient modelling of batch flotation. First, spherical particles were modelled, as a ‘baseline’, for different particle sizes and levels of hydrophobicity. In the second set of results, the induction period was decreased by a factor of up to ten, simulating flotation of angular particles. Flotation recovery was found to depend upon induction period in a complex manner. For highly hydrophobic or fine particles, the induction period for spheres was already so low that recovery was limited by other factors (e.g. bubble-particle collision frequency). Further decreases in induction period, as for angular particles, did not have a significant effect on recovery in these cases. By contrast, when weakly hydrophobic or coarse particles were modelled, the recovery was predicted to be greatly enhanced for angular particles, in comparison to spheres. For these particles the induction period was limiting recovery, so that the flotation rate constant could be improved directly by reducing the induction period. This is consistent with batch flotation experiments using Ballotini reported earlier. Therefore, when dealing with weakly hydrophobic particles or relatively large particles that are to be floated, an enhancement can be expected for more angular particle shapes. In such cases, judicious specification of the grinding circuit may improve the overall efficiency."

Jan 1, 2014

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 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 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