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By B. Rath

An effective process plan is an important part of maintaining consistent recoveries in mineral processing operations. Traditionally, Mineralogical studies are completed using chemical and metallurgical methods to monitor recovery and elemental distribution. The development of mineralogy and more efficient processes in mineral analysis techniques means that mineralogy is now more accessible as an efficient and comprehensive study tool. As operating costs increase and feed grades decrease it is important to maintain tight control of process and ensured maximum recovery is maintained at all times. Just a few days of losses in recovery caused by changes in ore type or processing conditions can have a large effect on total metal recovery and profit. Mineralogical audits can be used to minimize these losses by monitoring the fundamental behavior of feed ore on a regular basis. Smart use of mineralogical studies can develop mineralogical and ore type benchmarks in a detailed, which can be used in process control and monitoring. Geological ore types can be used to identify key mineralogical parameters that may be used in routine and cost effective analysis. Mineralogical systems ideally suited to this because of the depth of information on everything from modal mineralogy to locking/liberation characteristics and mineral associations. Mineralogical studies can equally be applied to specific unit operations within the process, which can allow more detailed information to be gathered on areas of the process that have been identified as critical. This will be especially effective for flotation or oxidation processes where process parameters can be very sensitive to small changes in mineralogy. This paper deals with the Ore Morphology, Ore Mineralogy, Gangue mineralogy, Photo micrographs under reflected, transmitted light and XRD studies Ore, Mineral studies of Sub grade Iron ore of Bacheli Complex, Bailadila Sector, India. Keywords: mineralogy, liberation, liberation studies, ore mineral, gangue mineral, morphology, jasper, ferruginous clay

Sep 1, 2012

By Erico Tabosa, Meng. Jun, Kym Runge, Matthew Brennan, Weiguo Xie, Dee Bradshaw

Turbulence and its distribution are of great importance in flotation cell design as they affect suspension of particles, air dispersion and particle-bubble collision rates, which in turn determine flotation performance. However, there is no mature technique to measure turbulence in three phase (liquid-solid-gas) systems such as in flotation cells. In this article, the authors present two new approaches that are suitable for measuring turbulence distribution in three phase systems and validate their applicability. The first technique uses a piezoelectric vibration sensor (PVS) to measure fluid kinetic energy standard deviation and the second technique applies electrical resistance tomography (ERT) to measure conductivity variation at a measurement position in a flotation cell. For the PVS technique, calibration of the sensor was performed to determine the values of parameters that were needed to calculate the force applied to the sensor. Then measurement was conducted in a 60L batch flotation cell and the results were compared with LDA measurement. This demonstrated that the piezoelectric sensor signal provides a good representation of fluid kinetic energy standard deviation at the position of measurement. For the ERT technique, conductivity distribution data was processed to give conductivity variations, which were then used to calculate fluid kinetic energy standard deviation at the measurement position. The spatial distribution of turbulence obtained by performing multiple measurements at different positions in the 60 litre batch flotation cell was found to agree with the PVS measurement results. These two techniques are potentially powerful tools for turbulence measurement in flotation environments, enabling a clearer understanding of turbulence’s influence on flotation performance to be determined.

Jan 1, 2014

By Xiao Jian Li, Dai Xiong Chen, Jian Wen Yang

In one kind of lead and zinc bearing polymetallic ore containing secondary copper, the characteristic of low sulfur, high zinc, and particularly the existing of secondary copper minerals can lead to lead concentrate with high content of zinc because the dissociation of Cu2+ in the grinding process may have an activation influence on sphalerite. Considering its process mineralogy analysis, a new process of seperation of lead and zinc has been put forward. The experiments focused on the analysis of the advantages and disadvantages of the inhibition effect of traditional adjustment reagent + zinc sulfate on activated sphalerite compared with new organic inhibitor, polysaccharide xanthate. According to the numerical calculation and test results, a reagent system of polysaccharide xanthates is developed, which has a good inhibition effect on Cu2+ activated zinc minerals, achieving high-efficiency separation of lead and zinc. A new reagent system and flotation process was developed under optimal conditions. Under the condition of the run-of-mine ore containing 2.37% Pb and 12.48% Zn, lead of 67.69% grade and lead concentrate with the recovery rate of 86.06%, zinc of 60.32% grade and zinc concentrate with the recovery rate of 96.15% were achieved.

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 Alejandro Uribe-Salas, Fabiola Nava-Alonso, Gloria Dávila-Pulido

This paper presents results of an experimental study performed on the role of calcium sulfate present in flotation water on sphalerite flotation in the Pb/Cu circuit (non Cu-activated sphalerite) and in the Zn circuit (Cu-activated sphalerite). In the Pb/Cu circuit calcium ions adsorb on the negatively-charged sphalerite favoring xanthate adsorption and therefore making sphalerite floatable; experimental measurements show sphalerite contact angle increases with calcium concentration while xanthate adsorption onto sphalerite increases with the increase of pH and calcium concentration. Gypsum (CaSO4·2H2O) eventually present due to calcium sulfate precipitation is not detrimental to flotation at this stage since it is negatively charged at pH 9 and therefore, does not adhere onto the surface of negatively-charged sphalerite. In the zinc circuit, Cu-activated sphalerite decreases its negative charge (or even becomes positively charged) and develops some hydrophobicity due to the polysulfide produced by Cu-activation. At this stage calcium ions do not interact with the mineral surface and therefore do not favor xanthate adsorption; nevertheless, precipitated gypsum particles do adhere onto the mineral surface, greatly affecting its floatability (e.g., contact angle). Addition of sodium carbonate to dissolve gypsum and to precipitate calcium as calcium carbonate, which disperses in the bulk of the suspension, effectively restores mineral hydrophobicity. SEM observations coupled with EDS analysis clearly illustrate and support the above sequence of events.

Jan 1, 2014

By Lala Zhao, Yuemin Zhao, Guangyuan Xie, Chusheng Liu, Chenlong Duan

"Screening is an important means of size classification used on granular or particulate materials. The vibrating modes of screen separator have a great effect on the screening process. Elliptical vibration mode is a complex motion mode which gets the common characteristics of both linear and circular vibration modes. However, the fundamental motion and screen penetration of the particles on the elliptically vibrating screen deck are still poorly understood. A numerical study of the motion of particulates flow along an elliptically vibrating screen deck is presented by means of a three dimensional Discrete Element Method (3D-DEM). The motion characteristic of the particle flow is analyzed at a particle scale. The effects of vibration amplitude, throwing index, vibration direction angle and screen deck inclination angle on the screening process are discussed. The results show that the particles average velocity increases linearly with the increase of vibration amplitude, throwing index and screen deck inclination angle, but decreases linearly with the increase of vibration direction angle. The screening efficiency is highest when the vibration amplitude, throwing index, vibration direction angle and screen deck inclination angle are 4.5 mm, 3.3, 40° and 6°, respectively. This work is helpful for developing a deep understanding of particle motion on the elliptically vibrating screen and for optimizing screen separator designs."

Jan 1, 2014

By Anuttam Patra, Romain Bordes, Andreas Fredriksson, Tommy Karlkvist, Krister Holmberg, Kota Hanumantha Rao

The present investigation aims to develop and distinguish mineral specific reagents with two functional groups for use in flotation of calcium containing minerals. For this purpose, a series of dicarboxylate-based surfactants with varying length between the carboxylate groups (one, two or three methylene groups) were synthesized. As reference, a surfactant with the same alkyl chain length but with only one carboxylate group in the polar part was synthesized. The adsorption behavior of these new reagents on pure apatite and calcite mineral surfaces was studied using Hallimond tube flotation, FTIR and ? potential measurements. The relation between the adsorption behavior of a given surfactant on a specific mineral surface and its molecular structure over a range of concentration and pH values, as well as the region of maximum recovery were established. It was found that one of the reagents, with a specific distance between the carboxylate groups, was much more selective for a particular mineral surface than the other homologues synthesized. This selective adsorption of a given surfactant to a particular mineral surface relative to other mineral surfaces as evidenced in flotation studies is substantiated by ? potential and infra-red spectroscopy data.

Jan 1, 2014

In this study, the effect of different regrinding conditions on the depression of fine pyrite at the cleaner stage was investigated. The regrinding condition was manipulated by different grinding media (stainless steel and mild steel). It was found that, after regrinding with mild steel grinding media, the flotation recovery of pyrite is much lower than with stainless steel grinding media, and it is more difficult to restore by adding more collector. This means, regrinding with mild steel grinding media may depress the pyrite flotation more strongly. The copper activation of pyrite during regrinding was also studied. It was found, that the mild steel grinding media is more beneficial to copper activation than stainless steel media. Additionally, the analysis of pyrite recovery based on the particle size indicated, that the fine particles are more susceptible to different grinding environments than intermediate and coarse particles and therefore are more easily depressed with a much lower flotation recovery.

Sep 1, 2012

By Mingxia Liu, Qi Liu, Tao Jiang

"In addition to physical parameters such as small mass and high specific surface area of fine and ultrafine minerals, chemical parameters such as the adsorption affinity of collectors on the minerals also plays an important role in fine particle flotation. In this study, we have examined collectors with two different ionized groups, carboxylate and hydroxamate, on the flotation of fine niobium oxide (pyrochlore). To facilitate comparison, two hydrocarbon radicals were tested: octyl and oleoyl, which led to four collectors that were studied: octyl hydroxamic acid (OHA), sodium octanoate (C8OONa), oleoyl hydroxamic acid (C18HA), and sodium oleate (NaOl). Small-scale flotation and isothermal microcalorimetric titration measurements were performed to determine the flotation recoveries of different sized pyrochlore and the enthalpic behavior after adsorption of the collectors on pyrochlore. It was found that the flotation performance of the carboxylate-based collectors was generally inferior to hydroxamate-based collectors. Sodium octanoate could not float pyrochlore irrespective of the particle size of the pyrochlore tested. With a longer hydrocarbon chain, sodium oleate was effective to float the relatively coarse pyrochlore (>20 µm) but its collection efficiency dropped sharply for particles smaller than 20 µm. On the other hand, the two hydroxamate-based collectors, octyl hydroxamic acid and oleoyl hydroxamic acid, showed good collecting ability to both the coarse and fine pyrochlore. The isothermal microcalorimetric titration studies indicated a consistent correlation of chain length with floatability of collectors for relatively coarse pyrochlore, as well as a positive relationship between the adsorption affinity and fine pyrochlore flotation recoveries. The key finding of this study was that efficient fine particle flotation could be achieved when strongly chemisorbing collectors were used.INTRODUCTION The first detailed study of the effect of particle size on flotation was made by Gaudin (1931) with sulphide ores. In 1942, Gaudin again demonstrated that (Gaudin et al., 1942) fine particles possess different flotation properties from larger particles. Since then the effect of particle size on froth flotation has been an important research topic by many researchers, e.g., Gaudin (1957), Miettinen et al. (2010), Warren (1976) Jameson (2010), summarizing the behavior of fine particles in terms of their low particle momentum, leading to low rate of collision with bubbles which reduces the chance of adhesion. The suggested remediation methods are mainly based on two approaches: increasing particle size or decreasing bubble size (Warren, 1976). Sand-fine splitting followed by separate flotation treatment of the sand and fines, using deep flotation cells, using starvation quantities of collectors, and using long flotation times, are also strategies to address the problems of fine particle flotation."

Jan 1, 2018

By A. Otsuki

This paper describes the evaluation method of dispersion and coagulation of silica nano-particles by means of interactive force apparatus. The apparatus measures the size of fine particles in aqueous solution or organic solvent of high concentration and/or low optical transparency. Other conventional apparatus for size measurements (such as, apparatus utilizing dynamic light scattering) are difficult to measure the size of particles in such conditions accurately, due to multi-scattering of light in the sample solution or solvent. The apparatus measures the interactive force between two surfaces, i.e. the gold-coated glass hemisphere and the brass flat plate, (which is fixed at the bottom of the sample cell). The apparatus has three parts, i.e. main part (which consists of electric balance, hemisphere and flat plate), control part (i.e. personal computer, piezo-stage controller and voltage supplier), and detecting part (i.e. multi-meter and oscilloscope). During the measurement, electric field is applied between the hemisphere and flat plate, and thus dielectric particles are arranged toward the direction of electric field in the area between two plates. When the two plates are close to each other, two different forces (i.e. repulsive force and attractive force) will alternately act on particles due to the structure change of the particles. The repulsive force occurs when the structure of particles is stretched by compressive force; whereas the attractive force occurs when the aggregate structure is broken. The cycle of the repulsive and attractive forces is a primary size of particle or size of aggregate, which depends on the degree of agglomeration. The measured size of particles, which is varied depending on their degree of dispersion and coagulation, determined the characteristics of the silica particles. In this research work, the effect of size and concentration of particles in aqueous solution on the degree of dispersion and coagulation of the silica particles were investigated. Spherical silica particles were selected for this investigation due to their variety of size. This apparatus can be used to evaluate the degree of dispersion and coagulation of other nano-particles in various solvents in many process industries.

Jan 1, 2014

By Takaaki Wajima

The slag was attempted to be converted into the adsorbent for phosphate removal from aqueous solution using the alkali fusion method. The slag was mixed with NaOH powder (NaOH / Slag = 1.6), and then the mixture was heated at 600 ? for 6 h to prepare the precursor. The precursor was stirred at room temperature in distilled water to synthesize the adsorbent, and the removal ability of the obtained adsorbent for phosphate from aqueous solution was investigated. The products, including hydrocalumite and calcite, were synthesized, and the removal efficiencies of the adsorbent for F- and PO43- showed higher than those of raw BF slag, especially removal of PO43- are excellent (99 %), while the removal of Cl- , SO42-, NO3- and Br- was minor. The adsorbent could remove PO43- selectively in the co-existing solution of Cl-, NO3-, F-, SO42- and Br-.The equilibrium adsorption capacity of the adsorbent for PO43- was extrapolated using Langmuir and Freundlich models, and experimental data are found to fit Langmuir than Freundlich. The calculated maximum adsorption capacity of the adsorbent for PO43- is higher than other adsorbent reported previously. The high affinity of the adsorbent for PO43- in aqueous solution was caused by the formation of hydroxyapatite [Ca5(PO4)3(OH)] and brushite [CaHPO4?2H2O]. The prepared adsorbent is expected to be anew inorganic adsorbent for the removal of phosphate ion from wastewater. Keywords: Blast furnace slag, Alkali fusion, Phosphate removal, High selectivity

Sep 1, 2012

The flotation of nickel sulphide minerals is normally difficult in the presence of serpentine minerals due to the coating of serpentine particles on the nickel mineral surface. To improve the flotation, dispersants such as polyphosphate and carboxy methyl cellulose are normally used to remove the slime coating. However, in the flotation using high ionic strength process water, these dispersants are invalid due to their ionic nature. In this study, a new type of non-ionic dispersants, Pluronic triblock copolymers were examined with an objective of improving the flotation of ultrafine pentlandite (a nickel sulphide mineral) in the presence of lizardite (a serpentine mineral) in saline water. Three Pluronic triblock copolymers varying in solubility and hydrophile-lipophile balance (HLB) values were studied by flotation tests, settling tests and froth measurement. It was found that two of the copolymers improved pentlandite flotation against lizardite, and one copolymer deteriorated the flotation. The effect of Pluronic triblock copolymers on the flotation was actually linked to their dispersibility and foamability, which were governed by their physical properties. The two copolymers with a higher solubility or HLB value produced more stable mineral suspensions and more stable froth in the flotation resulting in better nickel grade and recovery in both rougher and cleaner flotation. Keywords: ultrafine particle, flotation, slime coating, dispersion, saline water, triblock copolymers

Sep 1, 2012

By Masakazu Niinae, Kenji Aoki

"Electrokinetic soil remediation by electroosmosis and ionic migration is restricted to soluble substances. At a higher pH, the soil particles sorb more heavy metals than at a lower pH and the precipitation of heavy metals are promoted. Both mechanisms make heavy metals immobile, rendering cleanup more difficult and electrokinetic extraction inefficient.In this study, the effectiveness of introducing a complexing agent to enhance the removal of cadmium from kaolinite in the region of neutral pH by ionic migration is examined. The complexing agent selected was ethylenediaminetetraacetic acid (EDTA). The investigation was carried out in a laboratory-scale column containing kaolinite contaminated with cadmium. As the results of the study, cadmium migrates toward the anode without accumulation of cadmium and is successfully removed at the anode reservoir."

Jan 1, 2003

By N. T. Beukes, W. Banda

Recovery of Co from slag is a recent advancement in the extractive metallurgy of nonferrous metals. In this study a DC arc technology at laboratory scale has been applied to investigate the selective recovery of Co from slag, under three different flux types with an emphasis on influencing the activity of FeOx, SiO2 and CoO in the slag. It is known that reduction of slag by carbon is only up to a certain level after which, the recovery will depend on the chemistry of the slag, hence the need to modify the slag chemistry. Two power settings were employed to induce higher temperatures and aggressive agitation. The results were interpreted by comparing how much Co and Fe was in the slag and alloy. TiO2 reduced the amount of Fe in the product alloy compared to when CaO and CaF2 were used. The change in power did not seem to have had a major effect on the recovery although the amount of material lost to flue dust was more at a higher power rate.

Jan 1, 2003

By N. Ahmed

"This paper is concerned with the drainage behaviour of gangue mineral in the froth phase. Experiments were carried out in a continuous laboratory flotation cell in which froth depth and bubble size can be changed independently. The fraction of solids returning from the froth to the pulp zone was expressed using a rate constant by considering the appropriate froth regimes. A mixture of hydrophilic solids (silica) and floatable particles (glass ballotini) was used as a flotation feed. Samples of glass ballotini of different hydrophobicities were obtained, using controlled silanation. Three samples, with contact angles of 50, 66, 82 degrees, were used. The effect of the initial bubble size (pulp bubble size), concentration of gangue mineral in the froth zone, and froth depth on the drainage of silica, were also investigated.Typical results obtained from this study is shown in the figure given below. In this figure drainage rate constant for the entrained solids in the presence of particles of the three hydrophobicities is plotted against froth height. As observed, the drainage rate of the entrained solids increases considerably with an increase in the degree of hydrophobicity. Concerning the effect of pulp bubble size on the drainage rate of entrained solids, larger bubbles always give higher drainage rates due to formation of relatively loose froth structures which allows gangue particles to easily move down to the pulp zone. Conversely, smaller bubbles exhibit lower drainage rate constants, in particular at shallow froth depths."

Jan 1, 2003

By N. Kgabi, F. B. Waanders, E. Vinken, A. Mans

"Mössbauer and SEM identification of the iron mineral phases present in South African coal fractions from the Free State, Gauteng, Mmpumalanga, Natal and Waterberg coal fields, as well as from ash samples from coal used in the Lethabo power plant, containing a large amount of inorganic matter, was conducted. The iron is mainly associated with sulphur in the mineral but the amounts of these and other minerals vary considerably in coals from diverse origins. By means of Mössbauer analyses the iron bearing minerals were identified as pyrite, jarosite, illite and ankerite. In the SEM analyses quartz, associated with various clay minerals was identified with differences in abundance found between the coals from the different locations.The fly ash, produced at the high combustion temperatures in the power plant, gave rise to a spectrum, typical of a glass. SEM analyses showed that agglo- meration of the fly ash was due to the presence of Ca in the coal. The lab. produced fly ash was combusted at temperatures ranging from 200-1 200°C and the pyrite changed partially to hematite and partly into the glass due to the presence of the quarts and the clay minerals. A similar spectrum as the power plant fly ash spectrum was obtained.In the weathering experiments the pyrite changed to a sulphate component in a very short time during air drying."

Jan 1, 2003

By Anatoly N. Vinogradov, Vyacheslav A. Tsukerman

The North-West Russia for 70 years is one the main producers of Cu, Ni, Co, Al, P, REE, Zr, Ti, Ta, Nb, Fe ores and other minerals in the Europe. The largest mining companies locates in the Murmansk region, and they extracts about 100 mln. tons of ores and damps up to 250 mln. tons of waste annually. Nevertheless an environmental situation in the region is stable due to rational management and treatment of wastes on a base of the Noosphere Concept for Nature-using suggested by Vladimir Vernadsky. The Concept was performed practically in the Fersman’ scheme of “non-waste mining and metallurgical complex”, published in the monograph “Minerals of the Kola Peninsula: current status – analyses – prognoses” (1941) and served till now as a sort of “Bible” for industry managers lightening a strategy for an industrial “trophic chain”. The recent status of this scheme is shown on the picture below, and one can see that our concept is coincide with modern ideology known as the “Industrial Ecology”. Moving along this mainstream in the Kola Peninsula since 1929, when the first mining company “Apatit” was established, we provided the water close circuit in mineral dressing plants, hydrometallurgical treatment of slag and tailings, productions of building materials and adsorbents of wastes. The innovation set of technologies designed by the Kola Science Centre allow recently to involve tailing damps in re-exploitation as the technogenic deposits of valuable raw materials for fertilizers, tanning and cleaning agents, pigments, concretes and etc.

Jan 1, 2003

By Xiaodong Jia, Richard A. Williams

"The packing of particles is a fundamental property of a material or system made up of particulates because it underlies many other physical properties of that material or system. Despite being ubiquitous, particle packing has not been an easy subject to study either experimentally or theoretically, except for a few regular shapes.This paper describes the recent developments, arising from research at Leeds, in the computer modelling of packing of complex shaped particles and prediction of physical properties of the structures represented by the packing. The computer model DigiPac, is capable of packing particles of any shapes and sizes in a container of arbitrary geometry. Figure 1 shows a few examples that are relevant to the mining and mineral industry.The ability to predict packing structure of real particle shapes and to compute directly some structuredependent physical properties (such as liquid permeability, mechanical strength/stability, compaction and sintering, dissolution and leaching, etc.) is obviously highly desirable and has significant potential in industrial applications. Examples are presented relating to the packing of granular materials.The mining and mineral engineering industries are well placed to exploit this advance in digital packing and simulation since they deal primarily with asymmetric and complex particulate mixtures. In the future we expect to see a number of developments in this area including:Algorithms that can optimise packing to achieve user-defined propertiesA more rational approach to determining flowability of complex powdersUse of these more realistic packing algorithms linked to blast and crusher design"

Jan 1, 2003

By Bronwynne K. Williams

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

Jan 1, 2003

By Aziza A. Yousef, Suzan S. Ibrahim, Mahmoud A. Arafa, Mohamed A. Abdel Khalek

Due to the shortage of fresh water in the Middle East, seawater has been used as an alternative in flotation beneficiation. The flotation process requires about 7 m3 of water/mt ore. This article aims to study the effect of seawater cations and anions on the flotation. Natural pure francolite, calcite, dolomite and quartz were characterized by chemical, thermal and x-ray diffraction analyses, surface area, solubility and zeta potential. Synthetic seawater was prepared with the major chemical composition similar to natural seawater as follow; 2.45% NaCl, 0.52% MgCl2, 0.41% Na2SO4, 0.116% CaCl2 and 0.07% KCl. Also, natural seawater was used in application. The point zero of charge was estimated at pH 6.5, 7.8, 9.2 and 2.2 for francolite, calcite, dolomite and quartz, respectively. Calcium ions were released from the three minerals with Mg2+ and P2O5 3– released from dolomite and phosphate, respectively. The adsorption of collector, zeta-potential and floatability of pure minerals were studied. The effect of individual cations and anions predominant in seawater are studied on individual mineral or group. The troublesome Ca2+ and Mg2+ ions should be controlled by soda ash addition. Sodium silicate improved the selectivity of mineral mixtures and natural ore. At optimum conditions the calcareous phosphate ore yielded a concentrate of 34% P2O5, at 83% recovery with 0.61% MgO, from an ore assaying 25.3% P2O5 and 9.4% MgO. To minimize the Clcontent, fresh water of about 0.5 m3 /t was used and the Cl- decreased to about 0.09 %

Jan 1, 2003