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By Lina Chica, Arturo Barrientos, O. Bustamante

Hydrocyclone is a device commonly used in mineral processing industry. Underflow control plays a fundamental role in hydrocyclone operation. This affirmation supports the fact that hydrocyclone underflow has effect in some aspects of separation performance like capacity, split ratio, cut size and bypass. Hydrocyclone operation state is associated to underflow characteristics: air core formation and discharge shape. Many studies attempt to understand size separation phenomenon and the discharge influence but none of them has taken an energy point of view. This work presents the results of a mechanical energy dissipation for hydrocyclone operation from a mechanical energy balance. The experimental results related to Newtonian suspensions show that underflow energy dissipation does not control the operation because this magnitude is small compared to interior energy dissipation. However, discharge energy dissipation provides enough information to describe underflow conditions and its influence in separation conditions. In the modelling non dimensional parameters have been considered for hydrodynamic description and for geometrical and operation hydrocyclone characteristics. Energy dissipation from the continua media approximation results into a relevant concept to understand the hydrocyclone performance and improve industrial installations.

Jan 1, 2014

By Sun Chuanyao, Jia Muxin

Generally, if the bond valence (BV) between metal ion and oxygen of the mineral is greater than 0.8, only surface species –Me-O-H or –Me-O exposures on the mineral interface, if the BV is between 0.2-0.8, the metal ion exposures on the interface, and if the BV is less than 0.2 the metal ion dissolves into water. The PZCs of oxide minerals and island silicate minerals are determined by the bond valence of the bond in the mineral crystals, the higher the bond valence the lower the PZC of the mineral. So the PZC sequence of Al2SiO5 minerals is kyanite> andalusite> sillimanite. The general rule for framework silicate minerals is as: The higher the Al content, the lower the PZC of the mineral, when the ratio of Al to Si in the tetrahedron skeleton is below 1:3. The higher the Al content, the higher the PZC of the mineral, when the ratio of Al to Si in the skeleton is between 1:3 and 1:1. The general rule for layer silicate minerals is summarized as: the three-layer silicate minerals have much lower PZCs than that of the two-layer silicate minerals. The threelayer silicate mineral with the octahedron layer occupied by lower charged cations has lower PZC than that of the three-layer silicate mineral with the octahedron layer occupied by higher charged cations. The twolayer silicate mineral with the octahedron layer occupied by lower charged cations has higher PZC than that of the two-layer silicate mineral with the octahedron layer occupied by higher charged cations. The layer silicate mineral with Al substitution in the tetrahedron layer has lower PZC than that of the layer silicate mineral without Al substitution in the tetrahedron layer. Such pyroxene minerals whose M1 is occupied by a trivalence cation and the M2 is occupied by a monovalence cation has lower PZCs than those both M1 and M2 are all occupied by bivalence cations. Such hornblende minerals whose M2 is occupied by a trivalence cation and the M4 is occupied by a monovalence cation has lower PZCs than those both M2 and M4 are all occupied by bivalence cations. There is no Si4+ or 4 coordinated Al3+ exposures on the surface of framework silicate minerals, the metal ions of three layer or chain silicate minerals are compact between tetrahedron layersor chains, they hinder the metal ions to interact with oleate acid radical, the metal ion octahedron layer exposures on the surface of a two layer silicate mineral, but the the oleate acid radical can not attach to a metal ion by replacing a –OH- that connects three metal cations in the same time, So the floatability of such silicate mineral is bad. The metal octahedron chain style of an island silicate mineral affects it floatability, the mineral exposures octahedron chain metals with two dangling bonds in two directions floats better than the mineral exposures octahedron chain metals with two dangling bonds in one direction.

Jan 1, 2003

By Y. Foucaud, C. Eswaraiah, L. Filippov

Enhanced gravity separators such as Falcon concentrator which uses additional centrifugal force, are the most common gravity concentration techniques used for fine particles processing. Hence, understanding the kinetics and separation mechanisms within these separators is of paramount interest. Recent research yielded a predictive physical model for the Falcon Ultra Fine (UF) which however does not explain some results obtained with industrial ores. This study aims to identify the mechanisms involved in Falcon UF separation with the objective of confirming or rejecting the hypotheses on which the current model is built and suggesting potential points of improvement. The Falcon UF kinetics is investigated through the processing of complex low-grade and fine-grained ores from the Altenberg tin deposit (Germany), the Tabuaço tungsten deposit (Portugal) as well as a synthetic iron ore. Saturation tests are performed on the Falcon UF by controlling the separation efficiency in terms of recovery and enrichment ratio with time or feed mass. Results show an evolution of Falcon UF performance with time in contradiction with the stationary separation hypothesis on which the physical model is based. Observation of the concentrate bed suggests the presence of erosion figures in furrows which may play locally an active role in the separation. In terms of Falcon UF separation timing, three phases can be distinguished. First, upon initial feeding of the bowl, a bed quickly grows unselectively and ultra-fine particles are ejected from the bowl until the bed reaches its final profile. Next, actual separation occurs with selective concentration of dense particles. Finally, capture sites saturate and recovery drops. The evolution of partition curves over time confirms the existence of two separation mechanisms. First, differential particles settling within the flowing film responsible for the ejection of small size particles during the whole separation cycle which is already accounted for in the physical model. The second mechanism involved may be explained by the action of lift force, neglected in the physical model, which acts preferentially on coarse particles deposited at the surface of the bed resulting in coarser particles being rejected in the tailings. Hence, the addition of a lift force component to the existing model is suggested to account for this second separation mechanism.

Jan 1, 2018

Systemic process mineralogy study on Baerbulawu refractory hematite ore in Kazakhstan has been carried out. The ore contains Fe 41.34%, and 87.26 % of which exists in hematite. Most hema-tite occurs as fine or ultrafine grains and its average size is only 0.015mm. The gangue is mainly composed of quartz, mica, chlorite, kaolinite and other clay minerals. The liberation of hematite is only 66% when the ore is grinded to 75% ?0.074mm, while part of gangue is already liberated from hematite under this grinding condition, so these gangue can be cast away by magnetic separation in advance. Hematite will not liberate completely from gangue untill grinding fineness reaches 86% ?0.038mm, at the same time, free particles of ultrafine hematite tend to coagulate randomly with quartz and clay minerals, so appropriate dispersant is necessary to pre-vent hematite and clay minerals from coagulation. Based on the process mineralogy research, final technology flowsheet is high-intensity magnetic separation by coarse grinding?rough magnetic concentrate regrinding?inverse flotation, and an ideal index is achieved. The yield of final iron concentrate is 43.46%, and its grade and recovery are 66.76% and 70.55% respectively. The research result is also useful to other similar iron ores.

Jan 1, 2014

By H. Deng

Oxidized zinc ores are the main source of zinc metal except sulfides. To have a better understanding about the performance of smithsonite and the main gangue, quartz, in flotation, the aggregation behaviors of smithsonite and quartz in water were confirmed by different techniques (sedimentation tests and optical microscopy). The experimental results show that smithsonite and quartz particles aggregate in the pH range 7.5-11. The results of zeta potential suggest that the aggregation does not correlate with the DLVO theory, when the iso-electric point of smithsonite and quartz is 8.0 and 2 respectively. When the solution pH is less than 8.0, smithsonite has an opposite charge to the quartz particles. Electrostatic adsorption makes effort on these two kinds of particles according to DLVO theory. Whereas, solution chemistry calculation shows the pH range 8-11 corresponds to hydroxide formation, suggesting that this is the species responsible for aggregation. And their concentrations are much higher in sodium hydroxide system than that in sodium carbonate system. Aggregation of smithsonite and quartz due to the flocculation action of zinc hydroxide is proposed.

Sep 1, 2012

By Jia Muxin

The adsorption behaviors of metal ions on a silicate mineral and the flotability of a metalized silicate mineral with sodium oleate as collector are closely related to the structure of the silicate mineral. The adsorption isothermals of the metal ions on different silicate minerals are studied, the parameters of the isothermal give the information how many surface oxygen anions a metal ions is attached to, from this information and the structure of the mineral the site where a metal ion is attached can be guessed (The adsorption isothermals and adsorption behaviors with pH are fitted with Temkin, Frenudlich and Kurbatov equations respectively). Metal ions as Cu2+, Ni2+, Zn2+ are attached to the oxygen anions of surface species –Si-O– on the quartz surface, most of them coordinate to only one surface oxygen, their adsorption ability on quartz is low, but this metal ions on quartz surface protrude out of the surface perfectly, so their ability to combine with oleate acid radical is excellent. Quartz can be activated well by such metal ions. The isothermal of Fe3+ on quartz indicates these cations coordinates with more than two surface oxygen anions. This means the Fe3+ nucleates on quartz surface in the form of Fe(OH)3 colloid particles. The isothermals of Cu2+, Ni2+, Zn2+ Fe3+ on spodumene shows such ions coordinate with more than two surface oxygen anions, it indicate these ions may attach to the position where Li+ is formerly exists, such metal ions stay in a cave on the mineral surface, their adsorption abilities on spodumene are quite well, but they are affect by the oxygen anions of the two Si tetrahedron chains, the can almost not activate this mineral. These cations may attach on the site where Al3+ exists on the muscovite surface, just like spodumene, muscovite can not be activated well by such cations. Pt2+ has a large ion radius, as Pauling’s rules depicts polyhedron can not attach to Si tetrahedron well, the adsorption ability of Pt2+ on quartz is low and quartz is activated badly by Pt2+. On the other Pt2+ can adsorb well on spodumene and muscovite well and activated them well because it is not affected so bad by the tetrahedron oxygen anions of the minerals for their its large radius. The isothermal of Ca2+ on quartz indicates a Ca2+ coordinates with less than one surface oxygen anion, this means Ca2+ attaches on quartz mainly by physical adsorption. The adsorption abilities on mineral surface and the interaction abilities with oleate acid radical of the transition metal ions with the same valence are guessed to be determined by their d electron number, the rules should be d1<d2<d3<d4>d5<d6<d7<d8<d9>d10. Hydrogen bond may play an important rule in the activation of the mineral by HF and the interaction of the HF activated silicate mineral with collectors. The general rule is high bond valence and small metal ion radius surface species –Me-O can be activated well by HF with sodium oleate as collector. For example – SiIV-OH is neutral while –SiIV-FH+ and –SiVI-FH+0.33 are positively charged, the positively charged surface species are more likely to connect oleate acid radical via hydrogen bonds.

Jan 1, 2003

By S. Kondratiev

Mechanism of the action of nonpolar physically adsorbed reactants in froth flotation is under discussion in the paper. It is shown that their basic influence on flotation includes removing of the kinetics restrictions of the flotation complex formation. Experimental data and practical evidence reported in the paper sustain the proposed mechanism. There are discussed potential dependence of the kinetics of dixanthogen formation on platinum and its influence on the induction time (IT).

Sep 1, 2012

By P. A. Harvey

Previous studies have reported that inorganic electrolytes can enhance floatability of coal. The research has shown that the enhancement, if any, is highly dependent on changes in solution pH, type of electrolyte, and electrolyte concentration. The reasons for this are still not clear. In this study the floatability of coal particles in mono and divalent salt solutions was investigated. The zeta potential and hydrophobicity of the coal was measured experimentally, and a modified Hallimond tube was used to determine the floatability of coal particles by single bubbles, where the collision efficiency was equal to unity. The experimental information was used in conjunction with the Hogg-Healy-Fuerstenau equation to quantify the electrical double layer interaction. It was found that for low electrolyte concentration (less than 0.1 M) solutions the flotation recovery of coal particles was less than that for distilled water, and decreased with increase in concentration. Conversely, at electrolyte concentrations above 0.1 M, flotation recovery increased with increasing concentration (Figure 1). Both of these results are consistent with previous observations, but are inconsistent with expectations when considering the possible influence of electrical double layer interaction. Modelling of the system indicates that the electrical double layer is compressed with increasing electrolyte concentration, resulting in an increase in flotation recovery due to a diminishing of the (electrical double layer) repulsion between the bubble and the coal particles. Moreover, for electrolyte concentrations above about 0.1 M the electrical double layer is completely depressed and would have little further influence, if any, on the flotation process. Therefore, the electrical double layer interaction is not the principal determining factor for the flotation of coal in electrolyte solutions.

Jan 1, 2003

By Ivan Bonchev, Elisaveta Djurova, Evgeni Visariev, Viktor Stoilov

"Two types of slag cooling is used world wide - cooling in ladles and cooling in pits. The flotation comparison of the type cooling regimes was done at Aurubis Bulgaria. In Copper smelter Aurubis Bulgaria (Pirdop), the residual copper in the slags from Flash furnace and Converters is recovered by flotation. The slag flotation plant processes blend of three parts FSF and one part converter slag. The slag processing comprises: pit cooling, crushing, two stages grinding (autogenous and ball) and flotation. The copper content in flotation concentrate is over 20 % and in flotation tail is under 0.5 %. In order to improve the copper recovery, different cooling rate of the liquid slags should be achieved. Three cooling experiments with flash smelting furnace (FSF) slag have been done: two of them in pits with different volume and one cooling experiment in metallic ladle. The ambient air temperature during the cooling tests was from -4 to +4 OC. Laboratory flotation tests in open cycle were done with an aim to compare the slags behaviors cooled at different conditions. In this paper the effect of different cooling on the flotation process will be presented. The copper recovery and distribution by sizes in the tails, copper content in the rougher concentrate, and the concentrate yield are discussed."

Jan 1, 2014

By Y. Q. Yang

Jig is a kind of conventional and old gravity concentration equipment, which is mainly used in the preconcentration of medium particle fractions of low-grade nonferrous metal ore. In the past ten years, studies on jigs have made a great progress on separation of coarse and fine particle fractions. At the same time, pneumatic jigs have been widely used in processing of nonferrous metal ore. In this paper, pilot test study and commercial operation for several kinds of jigs used in Dachang con-centrator has been introduced. Dachang mining area of GuangXi province is rich in mineral resources, where many minerals exhibit various complex properties. Many elements such as Sn, Pb, Sb, Zn, S, As, Cu, In, Ag, Gd, Ag, Ga, etc, were found in the run-of-mine ore (ROM). At present, Dachang concentrator produces tin concentrate, lead-antimony concentrate and zinc concentrate. Other valuable elements get enriched and recovered in above concentrates. Dachang Mine with a mining operation history more than sixty years will end its mission on the rich ore resource exploitation. At present, low grade ores are porcessed in the concentrator, and the concentrator begins to run at a loss upon processing the low-grade and refractory ore. Heavy medium cyclones were used in the concentrator for processing 20-4mm fraction, Gongge jigs for 4-2mm fraction, and cone concentrator combined with spiral concentrator to discard the tailings of -2mm fractions. In order to minimize overgrinding, table flotation was used to recover some liberated cassiterites in a complex processing technology. Therefore, the concentrator is difficult to manage. Many years studies have shown that heavy medium cyclones and spiral concentra-tors can be replaced by sawtooth shaped wave jigs to discard 50% tailings to improve the grade of feed. And the feed was divided into rich one and poor one to minimize overgrinding of valuable cassiterites with different grinding mills. In this case, the recovery of the valuable minerals can get improved and the flowsheet was simplified. Moreover, the concentrator begins to make profit with reduction of cost. At the same time, pollution in the concentrator gets reduced and the working condition gets improved too. Sawtooth shaped wave jig was used in Changpo concentrator for replacement of cone separators and spiral concentrators to discard the tailings of -4mm fraction, and the yield of discarded tailings got improved from 30% to 50%. Grades of tin, lead and zinc in the tailings are lowered from 0.15%, 0.12%, 0.7% to 0.06%, 0.05%, 0.4% respectively, with a loss reduction of tin, lead and zinc from11%, 9%, 10% to 7.5%, 6%, 5% respectively, corresponding to the increasement of recovery of tin, lead, zinc from 52%, 50%, 55% to 56%, 56%, 62% respectively. Cost of the concentrator for processing one-ton ROM was therefore dropped from RMB155.28 to RMB119.74. Changpo concentrator lost RMB2.5 million in 2003, but it made a profit of RMB0.92 million in 2006 after the innovations. Batac jig was used in Tongkeng concentrator to discard the coarse tailings at 20-4mm, with a discarded yield of 35%, and the grades of valuable minerals got improved with a recovery above 95% for tin, lead-antimony and zinc.

Jan 1, 2014

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. A. Venter

Mineralogical studies indicate the Pt-Pd-Bi-Te class to react poorly on the flotation stimuli and indications are that these minerals are slow floaters. However, recent studies performed on a number of minerals from this class indicated strong interactions with potassium ethyl xanthate resulting in the formation of dixanthogen (only one of several xanthate species). The poor flotation response is not a result of poor interaction of xanthate with the surface. It is proposed that the oxidation products of sulfides in the process water interact with the PGM surface. To test this, the effect of thiosulfate (an important oxidation product of sulfides) was investigated by employing electrochemical measurements and FTIR spectroscopy. The electrochemical investigations indicate no strong effect of thiosulfate on the interaction of xanthate with the minerals surface as well as the reduction of oxygenthiosulfate is likely not responsible for the poor flotation response of these minerals in industrial plants.

Jan 1, 2014

By Zhaohui Qiu, Yaguan Ji, Hong Zhong, Qingxia Liu, Yada Liu

"Water is a necessary process medium in mineral processing. For the operations where fresh water is not available, sea water could be used as an alternative processing medium to replace the fresh water if we would have built a solid understanding of the interfacial science and flotation chemistry of sulfide minerals in sea water. In this research, micro flotation of chalcopyrite and pyrite in deionized water and sea water were investigated. For chalcopyrite, the recovery starts to drop from pH 10 in deionized water and from pH 9 in sea water, and the flotation recovery close to 100% before it drops. We can found from the results that chalcopyrite flotation is depressed much at pH 11 in sea water when much white precipitate is found. For pyrite, the flotaion recovery changs a lot in deionized water with 1*10-5 M potasium amyl xanthate (PAX) as collector. It’s relatively high at pH 8~10 compared with that at pH<8 and pH>10. While in sea water, the trend is almost the same as that of chalcopyrite. Zeta potential measurements and chemical equilibrium calculation were used to find out that magnesium hydroxide species coats on the surfaces at high pH in sea water are the main reason for depressing the chalcopyrite and pyrite flotation. Through understanding the interfacial science and the solution chemistry of sea water and its impact on processing efficiency, this research will not only helps reduce the use of fresh water to minimize the disposal of spent water for environment protection, but also enhance the recovery of valuable minerals in froth flotation."

Jan 1, 2014

By S. N. Sahu

Attempt was taken in this study to explore the misplacement phenomena in binary mixture in solid-liquid fluidisation system. The binary mixtures of hematite and quartz particles at different sizes were taken. The closed size range particles were taken to minimize the size and shape effect in fluidization. As both the minerals have appreciable density difference, the separation of both minerals with closed size range has an advantage. The experiments were conducted in different permutation and combination of different sizes of binary mixture to observe the fluidization phenomena. The samples were taken at different heights in fluidized zones and analyzed the distribution of particles of both minerals. The fluidization characteristics were evaluated with respect to operating and design parameters. It has been observed that when the terminal velocity of quartz and hematite particles is same or near to each other, then misplacement is significant. In general, the segregation index value is near to one, complete segregation takes place whereas this value is near to zero, complete mixing takes place. The experimental data were used to find out the segregation index for different size ratios of quartz and hematite particles and the values are within 0-1. When the size ratio is 1 or less, complete segregation takes place whereas this ratio is within 1.0-1.4, partial mixing takes place. Similarly, when the size ratio is within 1.4-2.0, complete mixing takes place whereas this ratio is within 2.0-4.6, then it moves towards complete segregation in inversion manner. Keywords: particulate fluidization, misplacement zone, bed expansion, terminal velocity, mixing characteristics, segregation index

Sep 1, 2012

By Stoyan Groudev

Two experimental plots consisting of a slightly acidic soil heavily contaminated with radionuclides (mainly uranium and radium) and non-ferrous metals (mainly copper, zinc, and cadmium) were treated in situ under real field conditions using the activity of some representatives of the indigenous soil microflora. This activity was enhanced by suitable changes in the levels of some essential environmental factors such as pH and water, oxygen and nutrient contents of the soil. The treatment was connected with solubilization and removal of the contaminants from the top soil layer (horizon A) due to the joint action of the soil microorganisms (mainly acidophilic chemolithotrophic bacteria) and leach solutions (diluted sulphuric acid) used to irrigate the soil. In one of the plots, the dissolved contaminants were removed from the soil profile through the drainage soil effluents and were subjected to cleaning by a constructed wetland located near this plot. In the other plot, the dissolved contaminants were transferred to the deeply located soil subhorizon B2 where they were precipitated as the relevant insoluble forms (uranium as uraninite, and the non-ferrous metals as the relevant sulphides) as a result of the activity of the sulphate-reducing bacteria inhabiting this soil subhorizon. This activity was enhanced by injecting water solutions of acetate, lactate, ammonium, and phosphate ions to this soil subhorizon.

Sep 1, 2012

By N. Raeis Hosseiny, S. H. Bassir

"Chador-Malu iron ore is one of the most important iron mines of Iran.About 98 percent of Fe in the ore is in shape of Magnetite, Hematite, Martite, aqua oxide of Iron and the other irons are with ferrous silicates, actinolite, cholorite and ferrous dolomites. 1% of Fe has replaced in pyrite. The phosphor distribution in the ore is non-hemogenous and its average in the whole of the deposit is 94%. It is in shape of Apatite.This mine contains considerable phosphor, which makes it useless for metallurgical uses. At this mine the phosphor is reduced in the iron ore at two steps. At the first step, magnetic part of the ore is separated from the gangues and phosphors by magnetic separator. At the second step, the ore is enriched by the flotation methods. Experimental flotation methods to obtain the optimum conditions are as follows:• Effect of Starch as Hematite depressant with ATRAC as Apatite collector• Effect of Sodium silicate as Hematite depressant with ATRAC as Apatite collector• Effect of ASAM as Apatite collector with Sodium silicate as Hematite depressant• Effect of ATRAC (BEROL) as Apatite collector with Sodium silicate as Hematite depressant• Effect of ASAM & ATRAC mixture as Apatite collector with Sodium silicate as Hematite depressant• Effect of Kcarbonate as pH-modifier• Final test to Optimize pH, Collector, DepressantAt this research we have found the optimum circumstance of the flotation of Chador-Malu iron ore in order to decreasing phosphors of iron oxide and floating of Apatite to make pure Hematite.To reach the optimum conditions, some tests were done with different amounts of pH, collector and depressant. The results are as follows:"

Jan 1, 2003

The addition of copper sulfate to mineral slurries in order to ?activate? sulfide mineral surfaces for enhanced collector molecule adsorption, and hence enhanced recovery via flotation, is a com-mon mineral processing practice. It has been established in a laboratory situation that the addition of CuSO4 in conjunction with xanthate collector increases the flotation rate of pentlandite as compared to the addition of collector alone. However, it remains unclear whether the addition of CuSO4has a similar effect within mineral processing circuits. We examine here the effect of pre-activation oxidation on the copper activation of pentlandite and monoclinic and hexagonal pyrrhotite. All activation experiments were carried out at pH 9 using a total solution content of copper ions equivalent to one monolayer (0.210 -4 moles, 110-4M). Copper loss from solution was extremely rapid in all cases with less than 10 % remaining after 10s. EDTA extraction and solution analysis clearly demonstrated that copper activation was via direct surface adsorption and not an ion exchange process, as is the case for sphalerite, and that most copper on the surfaces is in the form of Cu(I). ToF-SIMS analyses of the mineral surfaces subsequent to copper activation show increased surface oxidation on increased conditioning time prior to copper activation. However, there is a significant decrease in surface oxidation on comparison of samples that have otherwise been prepared in the same manner but where one has been exposed to copper solution rather than water. This suggests that copper activation stabilises the surface and reduces the propensity for oxidation. Regardless of the length of pre-activation oxidation time only Fe(III) (no Fe(II)-S) was observed by XPS analysis, indicating a highly oxidised surface layer dominated by Fe-O-OH species. The presence of Cu(II) on the mineral surface is indicative of the formation of Cu(II)-containing precipitates and indicates non-mineral specific activation resulting in increased recovery but lower grade. Mineral specific copper adsorption, as evidenced by the presence of Cu(I), is required to improve both grade and recovery. Prolonged oxidation prior to copper activation causes a reduction in the Cu(I) to Cu(II) ratio on the mineral surfaces as compared to either fresh surfaces or surfaces oxidised for 1 minute only. This strongly indicates that the copper activation process is less effective on highly oxidised surfaces.

Jan 1, 2014

By Sarthak Kaushik

Zeta potential measurements show that the isoelectric point of crandallite, in aqueous solution of 10-2 N sodium chloride is at about pH 5.5. Measurements of turbidity confirm the point of zero charge or crandallite. Calcium ions specifically adsorbed on the surface and thus changed the zeta potential and turbidity. From the measured data, it is confirmed that starch acts as a flocculent for crandallite. Oleic acid, which is a collector used in phosphate ore processing is weakly adsorbed on the surface of crandallite. This results in hydrophobic coagulation of particles resulting in a lower turbidity.

Sep 1, 2012

By M. H. Moys, H. Dong

"Discrete Element Method (DEM) has become a standard tool to simulate grinding mills in order to gain information about load behaviour, power drawn, etc. However, parameters necessary to run a simulation are not always readily available. For example, the coefficient of restitution used in DEM simulation from the literature ranges from 0.1 to 0.9 due to lack of accurate values. The lack of correct input parameters results in the fact that some simulation parameters are adjusted to match the simulation prediction with the experimental results. It is inappropriate to tune one single parameter arbitrarily in order to fit the prediction with experimental results. The correct value of parameters for DEM simulation should be established, and rigorous validation on simulation results by DEM needs to be done.The objectives of the ongoing project are to measure the coefficient of restitution at conditions analogous to grinding practice. Equipment has been built to measure the coefficient of restitution. A typical case of impact test showing the vertical position of a ball as a function of time is presented in Figure 1. The coefficient of restitution between steel ball of different sizes and the targets including steel liner (e = 0.91), mild steel block (e = 0.57) and rubber liner (e = 0.7) have been measured. The coefficient of restitution reduces to 0.38-0.52 when there is a layer of coal particles (1-2 mm) on the steel liner. The effects of ball size, drop height on coefficient of restitution are investigated. Then a DEM code is developed of several contact models to simulate the impact process. This code can reveal details on velocities (translational and rotational) and forces (normal and tangential) during the brief impact interval. Figure 2 is a comparison of the rebound rotational velocity between experiment and prediction by different models. The results can be used as DEM input and to assess contact models."

Jan 1, 2003

By Diogo R. Prado, José Aurélio M. da Luz

Drying operation can have a major importance in a mineral processing undertaking. The proper sizing of dryers can ensure the specified dewatering level without energy wastage. However, often the sizing of fluidized bed is done disregarding the actual residence time distribution (RTD) of the particles inside the reactor. In this case it is usual to adopt the average residence time as a design criterion. In this work, we have quantified the effect of residence time distribution on drying, ensuring that a previously adopted fraction of the particles remains inside the reactor for the required time lapse needed for drying. Design criteria such as particulate flow rate and drying time, taking into account the statistical distribution of residence time was studied, matching the thermodynamic and fluid dynamic aspects of the drying process. Experimental tests carried out have confirmed the RTD for a teetering bed as the same for a canonical ideal mixing system. Although the fluidized bed volume using the proposed formulation was higher than that found for the average time based procedure, the efficiency gain in drying has proven advantageous.

Jan 1, 2014