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By R. Van Hille, S. Lacour, A. E. Lewis, K. Peterson

"This paper compares thermodynamic modelling results with those obtained for copper sulphide removal from aqueous solution in both continuous and batch experiments at laboratory scale. Sulphide precipitation has been demonstrated to be an effective method for heavy metal removal. The advantages are the high degree of metal removal at low pH, low quantities of sludge formation, the ease of de-watering and low reactor retention time due to high reactivity of sulphides. However, the low solubility of sulphide species can lead to spontaneous nucleation of fines, which are difficult to remove.Theoretical modelling was carried out using ASPEN Plus™ and OLI systems Inc ESP process. Both simulators were used to calculate copper sulphide recovery and residual aqueous copper concentrations as a function of pH. The predictions were then compared with experimental results. Both simulations predicted that all of the inlet copper would precipitate as sulphide CuS(s) over the entire range of pH and sulphide: copper molar ratios investigated. The simulation results were strongly influenced by the number of chemical species and the nature of the thermodynamic data taken into account in the model.The continuous experimental studies were carried out in a fluidised bed reactor (FBR). Copper sulphate was reacted with sodium sulphide and the solid precipitated directly onto the pellets in the FBR. The use of sulphide was motivated by high sulphate levels in local acid mine drainage and the ultimate integration of the metal removal process with a biological sulphate reducing process that produces an aqueous sulphide stream.A maximum dissolved copper removal of 99.6% (AAS analysis) and a total removal efficiency of 95.8% (dissolved copper minus fines) were achieved. Stoichiometry of the precipitate was determined from SEM/EDAX analysis (atomic percentages) and was close to 1/1, irrespective of the operating conditions."

Jan 1, 2003

By S. S. Indi, D. Santhiya, S. Subramanian, K. A. Natarajan

"With the gradual depletion of the high-grade ores and finer dissemination of values in the leaner samples, it has become imperative to develop innovative approaches to process such complex ores. The beneficiation of complex sulphide ores containing copper, lead and zinc minerals, remains one of the most important challenges in base metals metallurgy. The advent of biotechnology in mineral processing has opened up immense possibilities to exploit such difficult-to-treat ores. Bioprocessing techniques thus hold promise as potential substitutes for the conventional technologies in vogue. Several types of autotrophic and heterotrophic bacteria, fungi, algae and yeasts are implicated in mineral beneficiation processes. Adopting a bioprocessing route to mineral beneficiation has attractive benefits, such as lower cost and energy requirements, environmental acceptability and operational flexibility.The interaction of sphalerite- and galena-adapted Bacillus polymyxa (B. polymyxa) cells with sphalerite and galena has been investigated through adsorption, electrokinetic and flotation studies. The amount of sphalerite-adapted cells adsorbed onto sphalerite and galena is found to decrease with increase in pH. On the other hand, the adsorption density of galena-adapted cells onto galena shows a feeble maximum around pH 8, and the amount adsorbed is marginally higher in the pH range of 8 – 11.5. In the case of sphalerite the amount adsorbed is higher in the pH range of 5 to 7. The adsorption density of both the adapted cells is higher for galena vis-à-vis sphalerite. Electrokinetic studies indicate significant surface chemical changes on the chosen sulphide minerals and the bacterial cells, consequent to microbemineral interactions. Selective flotation tests on a synthetic mixture of galena and sphalerite confirm that sphalerite could be preferentially floated from galena, using galena-adapted cells, but not with the sphalerite-adapted cells. The cells adapted to galena assay a higher polysaccharide content and are more hydrophilic, while the sphalerite-adapted cells have a higher protein content and possess greater hydrophobicity. Transmission electron microscopic studies have provided evidence in support of the differences between the cell surface characteristics of sphalerite- and galenaadapted cells (Figure 1). Possible mechanisms of interaction between the minerals and the bacterial cells are discussed."

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 P. Chris Pistorius, Johannes Sono, Rossouw Sono, J. J. Kobus

Different coal properties are important in SL/RN (coal-based rotary kiln) direct reduction of iron ore, and in electrical smelting of prereduced iron ore. These differences were highlighted when a plant which processes titaniferous magnetite had to change to different coal types after decades of operation. Laboratory simulation was used to evaluate two candidate coals, which were similar in volatile content and rank, but differed in reactive maceral content. Direct reduction was evaluated by isothermal experiments using a packed bed of ore and coal, measuring the off-gas composition to determine reaction rates and departure from equilibrium. These indicated reduction to be under mixed control, and quite sensitive to temperature (confirming that the coal reactivity is of importance). An aspect of electrical smelting was assessed by determining dissolution rates of the coal in molten iron at 1550°C. Dissolution rates did correlate with differences in coal structure, as determined by X-ray diffraction, with the more ordered ("more crystalline") coal dissolving faster. The conclusion is that the coal which is more reactive during direct reduction is less reactive during dissolution. However, it is concluded that controlling the temperature during direct reduction offers a feasible method to reconcile the two process steps.

Jan 1, 2003

By G. S. Hansford, G. E. Searby

The rate of bioleaching of pyrite at 70ºC by a thermophilic archaeal culture was measured as a function of the solution redox potential by the staged addition of pyrite to a batch system. The results were compared to the rate of ferrous iron oxidation over the same potential range to determine the applicability of the multi-sub-process leaching mechanism developed for mesophilic bioleach systems.

Jan 1, 2003

By Chuanyao Sun, Yang Yu, Zhen Guo Song, Wei. Ming’An

"Carbonate minerals are very important mineral source of extracting metal, radioactive element and rare earth elements. Furthermore,some carbonate minerals, such as calcite and dolomite, are common and important components of sediments and sedimentary rocks. Many flotation processes involve the separation of valuable minerals with carbonate minerals. So it is of great significance to the flotation theory and industrial practice to investigate the flotation behaviors of carbonate minerals. As regulators, metal ions play a major role in minerals flotation. The study of influence law of metal ions on minerals flotation is helpful to eliminate or utilize the effect of metal ions. In this study, calcite and smithsonite laboratory scale flotation, surface analysis and zeta potential determination in the presence of Fe(II) ion were performed to investigate the effect of Fe(II) on carbonate flotation. The results show that Fe(?) depresses the flotation of calcite and smithsonite. The depression effect of Fe species on calcite and calamine flotation can be improved with the increase of Fe(?) concentration. The zeta potential measurements and surface analysis show the existence of iron hydroxide products on mineral surface, which may be link to carbonate site instead of exchanging with calcium on the mineral surface. Fe species on the mineral surface inhibit the interaction between the reagents and calcite/smithsonite through the formation of surface precipitation coating on the calcite/smithsonite surface when the Fe(?) concentration is higher."

Jan 1, 2014

By Thomas Pretz, Alexandra Pehlken

Sampling of municipal solid waste is known to be difficult to sample if it has to be representative. When dealing with municipal solid waste, the usual method is to study separately waste material below 40 mm and particles bigger than 40 mm. The material < 40 mm cannot be sorted manual and is termed the “fine fraction”. The particles > 40 mm can be separated manually and are usually sorted into pre-defined groups of materials. These groups can be defined depending on the demand of quality assurance. But standardisation of procedures is not far progressed, even for the widely practised sorting methods.

Jan 1, 2003

By Katsunori Okaya, Toshio Inoue

"Movement of mill charge in the centrifugal mill is essentially dissimilar from that in the vibration mill with circular path despite the apparently similar mode in the motion of mill body. This dissimilarity is the reason for the substantial advantage regarding the comminution intensity of the centrifugal mill over the conventional vibration mill accounting approximately to one order of magnitude.Bradley et al. (1983) developed a math model regarding the mill charge as a lump. This model is presented in a simple equation with which motion of the mill charge can be predicted in terms of the parameters describing the specification and the operation of the centrifugal mill. This equation can be used to explain the power draft of the mill as well as the stability of mill operation. More recently, on the other hand, a numerical simulation technology called discrete element method (DEM) has become a vital vehicle for estimating the motion of the grinding media in the mill. The authors developed a mill simulator called ‘Mill Solver’. Mill Solver is designed to simulate various types of mills including centrifugal and vibration mills. The principle of this simulator is to calculate individual kinetic events of interaction of balls in the mill in a minute time interval, hence the mill performance can be constructed for estimation."

Jan 1, 2003

By Gus Van Weert, Samuel A. Bolorunduro, David B. Dreisinger

"INTRODUCTIONAcid pressure oxidation of high-grade natural acanthite was investigated in the range of 110-150°C and in the sulphate media. High acidity and low pulp density were used to prevent the precipitation of silver.RESULTS AND DISCUSSIONTwo sets of acanthite specimens were obtained from La Valenciana and Ingleterra mines, Mexico. Pressure oxidation tests were conducted on 1 litre scale in a standard 2-litre Parr titanium autoclave.EFFECT OF TEMPERATURE ON THE REACTION OF ACANTHITEThe effect of temperature on the rate of oxidation is presented in Figure 1. The rate of reaction increased with increasing temperature."

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 Victor Avdokhin, Valery Morozov, Valery Stolyarov

"The adaptation-determination method provides for keeping given relationship between concentrations of ionic and molecular components of a pulp liquid and correction of parameter of the model on the basis of analysis of ore composition, technological parameters of flotation, and cost of valuable components.• optimisation program “ADDEFLOT” and combined analyzer of pulp “RA-931”An adaptation-determination method provides for two-level control of bulk and selective flotation of polymetallic ores. The lower level provides for control of reagent dosing on the base of control of ionic composition parameters in the pulp liquid phase. The control goal is to keep the basis relationship among parameters of ionic composition (ions A, B, C) in pulp liquid phase given by equations of type:• alg[A] + blg[B] + clg[C] = K (1)Values of a,b,c coefficients are uniquely determined by a physico-chemical model used. Kind of the model depends on mineral composition of an ore and reagent regime applied. As parameter of ionic composition, also values of one or two parameters (or their combinations) can be used, for instance, pH, concentration of sulfide ions, ions of collector.The upper level of control is based on calculation and use of technological results of selective flotation. At the level, an adaptation of the model (1) is conducted. A principle of the adaptation is in determining (and including in pre-setting function of the lower level) such value of K parameter, at which maximal economic effectiveness of the process is reached. As a criterion of economic effectiveness of the process, a function of losses of several valuable components, taking into account cost of the metals lost, is used. For 2-component ore, in simplified form, the function is as follows:"

Jan 1, 2003

By Nóra Schreithofer, Kari Heiskanen

"INTRODUCTIONThe knowledge of the adhesion forces between particles and bubbles is of key importance in the improvement of flotation models. The development of the Colloidal Interaction Force Measurement Apparatus (CIFMA) opened the possibility to quantify the adhesion forces between particles and bubbles. The aim of this study was to examine the effect of three main variables: the approach velocity, the loading force and the loading time on the adhesion force between an air bubble and a hydrophobized silica particle."

Jan 1, 2003

By Stefan Mutz, Thomas Pretz, Jörg Julius, Frank Hilbk-Kortenbruck, Aachen, Hartmut Harbeck

"The annual global production of primary aluminium was about 22 million tons in the year 2000. This represents the second largest production rate in the world market after steel. Experts are predicting that the global demand for aluminium will rise in the near future.In contrast to other metals such as copper, the recycling of aluminium is considered relatively difficult. There are two main alloying groups, namely cast and wrought. In the case of aluminium it is important that the constituents within the scrap aluminium to be smelted are clearly identified. Within the secondary remelting process alloying does take place, but a removal of unwanted metal constituents is problematic. Therefore mixed aluminium scrap (not genuine in-house collected material) can only be used to produce cast aluminium. Thus, in other words a down-cycling of wrought (extrusions and rolled) products occurs. However, in spite of these difficulties there is an increasing trend to produce aluminium from secondary scrap (approx. 35% in Germany). Similar trends have been identified in the USA and other industrialised countries. This development is mainly caused by the high energy consumption for the production of aluminium from bauxite. Producing aluminium from scrap is saving about 95 % of the energy in comparison to the processing of primary raw materials.An improvement in sorting technology is necessary to separate wrought and cast alloys of aluminium as the absolute amount of recovery from old scrap is higher than the demand for cast.This contribution presents some alternative methods, utilizing automatic picking technologies, which will be used to separate secondary aluminium in the future. During the recent years, some major progresses have been made in automatic picking technologies for different applications in the processing of primary and secondary materials.For the sorting of aluminium scrap a special additional sensor will be necessary. The best detection will ultimately be based on online elemental analysis of single particles. First investigations in the field of laser based systems for these applications have already been performed several years ago. One of the laser based techniques is the laserinduced breakdown spectrometry (LIBS)."

Jan 1, 2003

By P. M. Solozhenkin

"Galvanochemical process (GChP)) cleaning of sewages is realized in the field of shortcirquited galvanic elements from the mixture current the materials place in purification’s solution and form multitude galvanopairs without external electric field in presence oxygen of the air. The galvanochemical process is electrochemical process utilizing galvanic pairs: coke - iron, iron - copper and others and process does not require chemical reagents.The effect of basic parameters of the cleaning effectiveness have been studied depending on oxidizing of galvanopairs. Adjusting nature, type of galvanic pairs and forming three component system possible to enlarge emf circuits to 2.378 V.The role of ?2, as basic agent, for generation of hydrogen peroxide and hydroxyl ions.It was stated, that removing of metal ions from solutions occur mainly on account of sorption and hydrolytic sedimentation of iron oxihydrates.Determined separate stages of the process: coagulation, sorptions of admixtures on freshly formed ferric oxides and oxidizing destruction of organic components of effluents in presence of ?2 ? ?2?2. Shown efficiency of the method for removing of Cu, Cr, Ni, Zn, As ions, as well as fluoride, phosphate and cyanide anions and oil products, surface-active and flotation reagents. Cleaned water can be recycled for some processes non-critical toward residual concentration of admixtures, as total salt contents is lowered on 60-75 % and reaching limits of concentration for toxic components.The concept of high power unit creation was developed, and galvanochemical pulsator is presented. The pulsator is not expensive, and exploitation expences are low, as well as servise is simple with high effectiveness, and capacity. The galvanoflotation process is developing, combining galvanochemistry and flotation of hydrofobic admixtures (oil, surface-active agents).The galvanochemical flotators are presented."

Jan 1, 2003

By Dingwu Feng, Jannie S. J. van Deventer

"The effect of ultrasonication on reactions at solid/liquid interfaces was investigated by using an ultrasonic probe in two slurry systems, i.e. cyanidation of a refractory sulphide ore and geopolymerisation of metakaolinite. The surfactant dithiophosphate was used to render the gold bearing sulphide particles hydrophobic, in an attempt to induce the formation of cavitation bubbles directly at the desired surfaces. Oxygen was injected into the cyanidation system to improve the attachment of oxygen bubbles to the hydrophobic sulphide surfaces. Geopolymerisation occurs in highly alkaline solution with waste aluminosilicate oxides and silicates as the reactants. The process of geopolymerisation is believed to involve dissolution of Al-Si oxides from solid particles, diffusion of dissolved Al-Si complex from the solid surface into the gel phase, condensation of gel phase and hardening of the gel phase. It has never been investigated how ultrasonication affects the above steps in synthesising geopolymers, despite a number of papers dealing with sonochemical synthesis of materials. The introduction of power ultrasound into such slurry systems is expected to result in advanced geopolymer materials.In the cyanidation of the pyrite concentrate, the kinetics of gold extraction were significantly enhanced in the presence of ultrasound, due to the prevention of passivation and the enhanced dissolution of sulphides. Cyanide consumption was significantly reduced with ultrasonication, owing to the oxidation of soluble sulphides to sulphate, minimising the cyanide consumption by sulphides. With oxygen injection, ultrasound significantly enhanced the leaching of gold from the pyrite concentrate, as oxygen could enhance the formation of the oxidation radicals by ultrasonic cavitation. In the presence of dithiophosphate, ultrasound further improved gold leaching in the oxygen-aerated system. Dithiophosphate could selectively adsorb at gold host sulphide surfaces, and make the surfaces hydrophobic. As a result, the ultrasonication effectiveness could be enhanced through forming cavitation bubbles directly at the interfaces."

Jan 1, 2003

By James A. Finch, Linda Restrepo, Mitra Mirnezami, Amy Buchanan, Maryam Hashemi

Settling rate studies on slurries from Cu/Zn flotation plants occasionally reveals two aggregation maxima at pH 8-10 and 10-12 (Figure 1). From measurements on sphalerite and silica suspensions the double maxima could be replicated. These maxima correspond to the effects of Zn and Mg ions. The aggregation mechanism of both ions is related to the formation of the corresponding hydroxide precipitate. A combination of chemical and electrostatic bridging by the hydroxides is considered to be the aggregation mechanism.

Jan 1, 2003

By Willis Forsling, Prabhakar Swarna, Hanumantha Rao Kota

"The solubility of wollastonite and its Hallimond flotation behavior as a function of dodecylamine concentration and pH are examined. The flotation response is characterized by adsorption and surface energy in the presence of amine. The methods of UV-Visible and FT-IR spectroscopy for adsorption and sessile-drop contact angle for surface energy estimation are employed.The results of wollastonite dissolution clearly showed its non uniform dissolution. The surfaces are depleted with calcium ions and became rich in silicon within 10 min of flotation time. Maximum flotation of wollastonite corresponds to a half monolayer coverage of amine, which is substantiated by the surface energy parameters as shown in figure 1."

Jan 1, 2003

By Remmerswaal, U. Boin, M. B. G. Castro

"To design sustainable products that can be recycled with high resource efficiency, low environmental impact and economic feasibility, the choice of materials and materials combinations, made in the design stage, is fundamental. The products we design, manufacture and use now will be the resources of the future. Designers are able to select materials for a product according to the many functional requirements they must fulfil. But they have a limited knowledge of the recycling processes and its requirements regarding quality of the secondary material streams. Resource Engineers have to manage the processing of these streams, that are becoming more complex with the increasing variety of materials and decreasing size of components. After mechanical separation of the materials streams resulting from shredding of EOL (endof- life) products, there is always a degree of contamination, from two possible causes:Incomplete liberation: the bonds between different materials combined in a component are not completely destroyed by shredding, resulting in some particles containing two or more materials attached;Separation efficiency: the mechanical separation processes are not able to separate perfectly the many material particles; there are always a number of foreign particles in the recovered streams.Sometimes, those contaminants cannot be removed by the industrial metallurgic recycling processes, and a more serious problem occurs when the contamination levels compromise the recycling of the material stream by lowering its quality (i.e. the properties of the recycled material will be lower due to the contamination). As a consequence, the material must be diluted in virgin raw material and/or used in a less demanding application (downgrading), causing resource depletion and increased energy use, waste production and recycling costs. In order to make the best choice of materials combinations for a product, a systematic approach is necessary, that can close the gap between the knowledge areas of Product Design and Recycling Technology."

Jan 1, 2003

By Ashton M. Swartbooi, Robert van Hille, Alison E. Lewis

"Nickel production by precipitation using hydrogen reduction generates an ammonium sulphate solution containing approximately 2g/L of nickel, and 1g/L of cobalt as an impurity of the process. Sulphide precipitation is an effective method for heavy metal removal, especially when compared to hydroxide processes: metals can be removed from solution at relatively low pH levels, small quantities of sludge are formed, and due to the high reactivity of sulphides the reactor retention time is reduced. However, the low solubility of sulphide species can lead to spontaneous nucleation of fines (due to higher supersaturation levels which are difficult to separate from solution, leading to reduced process efficiency. Using a fluidised bed reactor, fines formation can be minimised as the pellets provide a large surface area and promote heterogeneous nucleation.A synthetic nickel-cobalt ammonium sulphate solution was reacted with two forms of sulphide reagent: (a) a liquid sulphide solution and (b) gaseous hydrogen sulphide. A range of factors (including pH, reagent concentrations, metal to sulphide molar ratio, flow rates and recirculation rates) influencing the efficiency of the precipitation reaction have been studied. The efficiency of the precipitation reaction was measured using both metal recovery and fines formation as indicators.Figure 1 shows the effect of decreasing the metal:sulphide ratio (at constant SS = 2.725e+17), on the metal removal for liquid sulphide. By decreasing the metal:sulphide ratio, up to 99% removal of both nickel and cobalt could be achieved.These results also indicate that the precipitates that formed were polysulphides, since no sulphide was present in solution after the experiment. This would also indicate that a lower metal:sulphide ratio would be more favourable. However, decreasing this ratio (at constant metal concentrations) would lead to an increase in the fines concentration, because of increased supersaturation levels induced by the higher sulphide concentrations. To decrease the supersaturation, dilute solutions of either reagent would be employed."

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 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