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By P. M. Solozhenkin, V. P. Nebera, V. D. Skorohodov

"Aqueous dispersions of air specifically prepared on the basis of flotation reagent solution acquire active properties in relation to the solid surface and may be imply as a medium for flotation ores. Such aerated solutions were defined as Activated Aqueous Dispersions of Air (AADA) with 5-6:1 ratio and the procedure of mineral separation was defined as a flotation process under non-equilibrium conditions. These procedures differ from conventional flotation mainly in reagent interaction with minerals through their adsorption films on gas bubbles simultaneously forming flotation complexes. Gas-liquid mixture is kept till an adsorption layer of reagents close to the limit value is formed on the surface of bubbles. The theoretical basis of AADA is considered.The results of two-phase gas- liquid mixture (AADA) were studied. Two versions of AADA were considered. Electrical surface potential of the air bubbles with the surfactant film, untreated minerals particles in Coulomb attraction and flotation complex formation were analyzed. Special flotation machines were constructed for separation of mineral suspension in air dispersion, whose effectiveness was confirmed in flotation of apatite waste of Kovdor ore. FK-9 machine introduced on Kovdor iron ore combine for the recovery of apatite from current departures of factory. The froth product contained 7.2 % P2O5, with recovery of 44 % apatite, which was processed for getting melted phosphoric-magnesium fertilizers."

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 Takashi Furuyama, Sukeyuki Mori, Tetsuo Ikejiri, Abel Bissombolo, Yoshitsugu Koga, Masamichi Hata

In Japan, the increasing number of automobiles newly put into circulation is followed by a larger amount of end-of-life vehicles from which valuable metals are being recovered in shredder and related plants. Nevertheless, the processing of these scrapped automobiles which has reach a recycling rate of about 75%, generates a huge volume of waste, locally known as .shredder dust., which is commonly dumped on landfills. The saturation and depletion of valuable disposal sites in the near future, as well as the social and environmental problems related to the accumulation of these residues disposals are a major challenge for the automobile shredding industry. To promote an alternative way for the management of these disposals, the authors have initiated and developed a system for their processing, on the basis that more than 90% of these residues are combustible materials that could be used as refuses derived fuel. The developed processing system points out the mechanical/physical separation of shredded automobiles residues into two streams by means of an ascending airflow passing through a vertical zigzag separator and, the compaction of the light-density fraction of materials (that is about 60% of auto shredder residue recovered as float products and mainly composed of cotton, sponges and light plastics) to form a refuse derived fuel (RDF), the density, calorific value and ignition loss of which are 1.19 g/cm3, 4470 kcal/kg and 60.7%, respectively.

Jan 1, 2003

By Hajime Miki, Mutia Dewi Yuniati, Tsuyoshi Hirajima, Keiko Sasaki

Acid mine drainage is mainly due to pyrite/arsenopyrite oxidation processes, and suppressing such processes is important issue. As a promising process it is reported that silicate ion can complex with catechol (1,2-dihydroxybenzene) and this complex is oxidized to a solid silica layer on the surface of those sulphide minerals. Detailed behavior was investigated from the result of electrochemical experiments. Results of polarization potential showed that oxidation peak can be seen only in the presence of both silicate ion and catechol addition at this peak potential and this peak can be identified as silicate-catechol complex oxidation to silica. Potentiostatic experiments indicated the dissolution kinetics of pyrite. Untreated pyrite dissolution rates were higher than pyrite treated with catechol and silica solution. To enhance the silica layer reaction on pyrite, the pyrite potential was held at 550 mV vs. SHE in catechol silica solution. This pyrite dissolution kinetics was almost the same as untreated pyrite. Potential hold followed by drying for 30 min process resulted in much lower pyrite dissolution rates. Drying is important for development of the silica layer. Analysis of this potentiostatic curve provided a way to estimate the thickness of the produced silica layer and kinetic information of treated/untreated pyrite. Untreated pyrite showed thinner initial layer thickness on the surface of pyrite (oxidized passive layer, not silica) and higher oxidative kinetics of pyrite compared with silica-coated pyrite.

Jan 1, 2014

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

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

Jan 1, 2003

By Michael Young, Rodrigo Araya, Cesar Gomez, Le Huynh, James Finch

The performance of flotation machines is closely related to the gas dispersion characteristics achieved in their operation. It is known that frothers play a major role not only in the size distribution of the generated bubble population, but also on the swarm rise velocity. A program to characterize frother effects on two-phase hydrodynamics (air-water) of Jameson cells was undertaken in a fully instrumented pilot unit installed at McGill University. Gas dispersion parameters (gas velocity, gas holdup and bubble size distributions) of the gas-liquid mixture generated in the downcomer were measured after its release into the separation chamber. The unit was operated under different conditions including gas velocity, liquid jet velocity and frother concentration (MIBC). Bubble size distributions for concentrations above the critical coalescence concentration (CCC) were narrow with Sauter mean diameter between 0.6 to 1.3 mm. The bubble size followed the general trend as encountered in other types of flotation machines, i.e., rapid decrease with increasing frother concentrations below 10 µL/L, and almost no change in size for concentrations above 30 µL/L. The CCC was between 10 and 15 µL/L. Strong correlations were found between bubble size and air-to-liquid flow ratio (APR), and between the bulk density of the aerated solution in the separation tank and the vacuum inside the downcomer. An equation is proposed to estimate gas holdup in the separation tank from vacuum and bulk density readings.

Jan 1, 2014

By Kazutoshi Haga, Atsushi Shibayama, Kosuke Nishioka, Yasushi Kihara, Altansukh Batnasan

The aim of this study was to investigate the feasibility studies of seawater in flotation of a 1.5 mass % of copper containing copper sulfide ore. Effects of seawater, various frothers, and different distilled water/seawater ratio on flotation of copper sulfide ore were studied. Surface properties of native copper ore and sea water soaked were examined by using FT-IR spectrometry. Chemical contents of the copper sulfide ore and after flotation were identified using XRD studies. XRD pattern showed that the main constituents of the copper sulfide ore are chalcopyrite (CuFeS2), bornite (Cu5FeS4). Flotation experiments were carried out using mechanical agitation flotation equipment with a mineral separation type flotation cell. Froth flotation experiment was conducted using calcium hydroxide was used as a pH adjuster, using methyl isobutyl carbinol (MIBC), dow froth 250 (DF 250) as frothers and potassium amyl xanthate (PAX) as collector for the copper recovery from the copper sulfide ore containing chalcopyrite and bornite. The results showed that the copper recovery by flotation was dependent on the flotation medium and frother. The main results showed that the copper recovery by flotation was dependent on the process water and frother. The copper recovery reached 97 % and 87 % in the distilled water flotation and seawater flotation with MIBC, respectively. For seawater flotation with DF 250, the Cu recovery achieved near 95 % and grade of Cu in the froth product after 5 min flotation was reached 29.8 mass %.

Jan 1, 2014

By P. Basarova

The attachment of bubbles onto a collecting surface is an ubiquitous natural phenomenon, playing a critical role in numerous practical processes. The goal of the project is to broaden the knowledge about hydrodynamic interactions between small bubbles and large solids that occur in nature and industrial processes. Focusing on collision processes between a single rising bubble (Db<1 mm) and a larger falling spherical particle in stagnant liquid, the theoretical model describing the bubble trajectory is given here. The model is based on analysis of forces acting on the bubble, and utilizes equation for the bubble motion. Mobile and immobile type of bubble surface mobility are considered. The calculated results are compared with the experimental data; here a high-speed video camera was used to capture the bubble motion and bubble-particle interaction. Very good agreement between experimental and calculated data was found. For both types of surface mobilities, the bubble deviation in the horizontal direction is nearly linear. The proportion constant is bigger for immobile bubble surface and increases with the bubble size. Furthermore, particular forces acting on bubble were studied. A similar course of relative bubble velocity and force impact was observed for identical bubble position. For cases when the bubble centre is close to the particle axis, only deflection in one direction is observed. When the bubble is reaching the maximum trajectory, the force ratio is changed. The bubble is firstly pushed away from the particle, but when it is within close distance from the particle, the bubble is pushed towards the particle.

Sep 1, 2012

By I. A. Podkamennyi, O. E. Kovalchuk, G. P. Dvoychenkova

"Using the methods of electron microscopy and IR spectroscopy, mineral components in the run-of-mine kimberlites and on the surface of diamonds were identified. The mechanism and sequence of mineral formation on the surface of diamond crystals were established. Systematization and classification thereof were undertaken for the first time ever.INTRODUCTION The high content of diamonds sized -5 mm in the kimberlite ores of Western Yakutia determines their processing depth in the size class 0.5 mm and finer [1, 2]. These diamonds are recovered by grease and froth separation based on the natural hydrophobic properties of the crystals. When refractory altered kimberlite ores are fed into the industrial process, the performance of grease and froth separation of the diamond ore greatly deteriorates. [4, 10, 15, 17]. Altered kimberlites are known to contain up to 90% of secondary minerals. This reduces by up to 40% the recovery of diamonds by grease and froth separation. [6].Diamond crystals from the grease and froth separation tailings were investigated. On the surface of the examined diamonds, hydrophilic mineral formations were identified, responsible for reduced recovery by physicochemical separation methods [3, 12, 18]. The aim of this study was to identify and describe the relationship between the composition of kimberlite ores and mineral formations on the surface of diamond crystals in order to systematize, classify, and then develop methods of removal in grease and froth separation processes. MATERIALS Following materials were examined in this study: - kimberlites of various material composition, - resulting slimes, - diamond crystals from kimberlite ore processing products."

Jan 1, 2018

By T. Suzuki

Acid leach liquors from spent lithium-ion batteries employing lithium cobalt dioxide (LiCoO2) as a cathode active material contain valuable metals such as cobalt and lithium, as well as common metals such as aluminum and copper. The objective of this study was to develop a hydrometallurgical process providing a high selectively between aluminum, cobalt, copper, and lithium from hydrochloric acid solutions. Batch experiment results showed that selective hydroxide precipitation approach was not suitable because a significant amount of cobalt and lithium was co-precipitated with aluminum and copper hydroxides. In contrast, batch experiments and the subsequent data analysis indicated that the sequence of solvent extraction circuits using PC-88A, Acorga M5640, and tri-n-octylamine (TOA) extractants effectively separates four metals of interest. In the first circuit of the proposed process, copper was selectively extracted by Acorga M5640 at the pH 1.0-2.0. Aluminum, cobalt, and lithium remain in the aqueous phase. In the second circuit, aluminium is selectively extracted by PC-88A at pH 2.0-2.5. For the separation of remaining cobalt and lithium, Acorga M5640 provided higher separation efficiency compared to PC-88A single extractant and PC-88A/TOA mixed extractant. However, the stripping efficiency of cobalt from the Acorga M5640 organic phase was found to be low (less than 10 %). Therefore, PC-88A/TOA mixed extractant rather than Acorga M5640 is an advisable choice for the separation of cobalt and lithium. Keywords: spent lithium-ion secondary batteries, solvent extraction, lithium, cobalt

Sep 1, 2012

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

By Xiaoping Xu, Tiansong Dong, Guosheng Wang

"Jianfengpo tin ore is located in Jiangxi Province, China. The cassiterite is fine and dispersed. It is hard to separate marmatite from a variety of sulfide minerals. Because the iron-containing sulfide minerals including pyrrhotite, pyrite and chalcopyrite are detrimental to the improvement of the grade of zinc concentrate. Besides, the presence of the iron oxides and ferro-carbonate minerals results in the difficult beneficiation of tin. Therefore, Jianfengpo tin ore is a kind of refractory cassiterite polymetallic sulfide ore. According to the properties of Jianfengpo tin ore, the technology process of "Sulphide ore preflotation-Bulk flotation of sulphur and zinc-Separation of sulphur and zinc -Magnetic separation-Gravity concentration" was developed to recover the valuable materials including marmatite, pyrite, magnetite, cassiterite and indium comprehensively. For the feed ore containing 0.87% Sn and 0.70% Zn, a zinc concentrate of 44.56% Zn with a recovery of 69.10%, a high-grade tin concentrate of 54.38% Sn with a recovery of 53.03% and a low-grade tin concentrate of 6.54% Sn with a recovery of 1.25% can be achieved in the batch flotation tests. In the industrial tests, for the feeding which contains 0.55% Sn and 0.65% Zn, the tin concentrate of 49.10% Sn with a recovery of 48.52% as well as the zinc concentrate of 45.11% Zn with a recovery of 60.10% can be produced. Thus some pyrite and magnetite concentrate are recovered as well. So Zinc, tin, sulphur and iron ores are recovered effectively by the technology."

Jan 1, 2014

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 Chen Zhiqiang, Luo Chuansheng, Chen Ziqiang, Liu Jianguo, Rao Jinshan

To comprehensively utilize the valuable resource in tailings, increase the economic benefit of mine, reduce the amount of tailings, prolong the service life of tailing dam, the comprehensive utilization of tailing resource is arousing the attention of more and more mines. Research of comprehensive recovery of feldspar and silica from Cu-Mo floatation tailings has been furthered. Technology of "De-sliming-Magnetic Separation-Reverse Flotation-Feldspar and Silica Separation" has been developed to utilize the resource. Slime is removed and reagents cost is reduced by de-sliming. The specific effective collector ZL is used in gangues reverse flotation, and GZ-818 is the collector in feldspar and silica separation. The grinding operation is vital to ensure the liberation degree of feldspar and to eliminate the reagents pollution on minerals surface. To a Cu-Mo flotation tailing assaying K2O 5.22%, Na2O 2.22%, Fe2O3 1.95%, Al2O3 12.05%, SiO270.66%, superfine K-feldspar and silica concentrates can be produced. The feldspar concentrate productivity is 29.67% assaying K2O 8.99%, Na2O 2.86%, Fe2O3 0.16%, Al2O3 16.99% and SiO2 68.92%. The silica concentrate productivity is 14.20% assaying 0.17% K2O, 0.04% Na2O, 0.01% Fe2O3, 0.55% Al2O3 and 98.17% SiO2. The technology provides technological reference model for the similar mines.

Jan 1, 2014

By David Deglon, Martin Harris, Mehdi Safari

This paper investigates the effect of energy input on the flotation of galena in a novel oscillating grid flotation cell (OGC). Oscillating grids generate near ideal hydrodynamic environments, characterised by turbulence which is relatively homogeneous and isotropic. Previous work was limited to quartz (-100 µm). Galena (-150 µm) was floated in the OGC at power intensities from 0.5 to 3 W/kg using 0.13, 0.58 and 0.82 mm mean bubble sizes (d10) and at three collector dosages. Results show that the effect of power intensity on flotation kinetics is strongly dependent on both particle and bubble size. For fine particles (-19 µm), increasing energy input increases the flotation rate at a low collector dosage but leads to an optimum at both the moderate and high collector dosages. For intermediate particles (+19-38 µm), increasing energy input has no effect on the flotation rate at the low collector dosage but leads to an optimum at both moderate and high collector dosages. For coarse particles (+38-150 µm), increasing energy input has no effect on the flotation rate at the low collector dosage and leads to a general decrease at both moderate and high collector dosages. Optimum conditions for fine particles are using small bubbles at a moderate collector dosage and an energy input of around 2 W/kg. Optimum conditions for moderate particles are using small bubbles at a high collector dosage and energy inputs of around 1.0 W/kg. Coarse particles do not benefit from agitation.

Jan 1, 2014

By V. Y. Dementyev

Laboratory and pilot-plant testing using a sample of gold-bearing semi-oxidized ore from a Russian deposit followed by a flow sheet and reagent flotation mode development to design a plant was carried out in IRGIREDMET in 2009-2010. According to the developed flow sheet low alkaline flotation conditions are recommended in order to activate the surface of sulfides. The pH lowering from natural (7.5-8.0) to optimal (4.6-4.8) value using sulfuric acid provides for an increase in gold recovery. Before CIL, a final flotation concentrate is pretreated using pressure oxidation. It was found that the use of recycled solutions from pressure liberation in order to create acidic conditions for flotation instead of sulfuric acid during pilot-plant testing is recommended. The flow sheet offers the detoxification of remaining pressure oxidation solutions together with the flotation tailings. The carbonates presented in the tailings significantly reduce the consumption of lime for detoxification and allows for the use of two tailings dams instead of three. The first is used for the tailings of flotation and pressure oxidation recycled solutions, which were detoxified together. The second tailings dam is used for detoxified cyanidation cakes of the flotation concentrate. It was found during pilot-plant testing that flotation under natural and acidic conditions provides for 88.9 percent and 93 percent gold recovery, respectively. 4.1Au percent increase recovery was achieved due to the reduction of gold losses with flotation tailings and better quality of concentrates.

Sep 1, 2012

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

"Acidic solutions for chalcopyrite leaching contain cupric, ferrous and ferric ions, and the oxidizing power of the solutions is indicated by a redox potential, determined by the concentration ratio of ferric to ferrous ions. This paper reviews our previous studies on the redox potential dependence of chalcopyrite leaching in sulfuric acid solutions. Leaching experiments indicated that copper extraction rate was accelerated by cupric and ferrous ions , and was higher at potentials below a critical value (critical potential) in the presence of these ions. This was in good agreement with the results of electrochemical measurements, i.e. in the anodic polarization curves for a chalcopyrite electrode, active-passive behavior was observed when cupric and ferrous ions co-exist, but the activation at low potential did not occur without these ions (Figure 1). The analysis of the AC impedance spectra for chalcopyrite electrode indicated that a high-resistance passive layer grows on the chalcopyrite surface without cupric and/or ferrous ions, and that coexistence of these ions causes a formation of another product layer and inhibits the passive layer growth at low potentials.These results are explained by a reaction model assuming the formation of intermediate Cu2S due to chalcopyrite reduction and the subsequent oxidation of the Cu2S. The critical potential corresponds to the redox potential of the Cu2S formation and the predicted values matched with the experimental results. Catalytic effect of silver ions on chalcopyrite leaching was also discussed based on experimental results and the above model."

Jan 1, 2003

By P. Gao, J. W. Yu

"Magnetizing roasting-magnetic separation is an important route for the beneficiation of refractory iron ores. In this investigation, a pilot-scale fluidized magnetizing roasting reactor was introduced and used to study the effects of roasting temperature and the flow rates of reducing gas CO and fluidizing gas N2, on the magnetizing roasting performance of an Anshan-type carbonate-bearing fine iron ore. The results showed that the hematite was almost reduced to magnetite by a gas mixture of 4 m3/h CO and 1 m3/h N2 at a roasting temperature of 540 °C. Under the optimized conditions, a high-grade magnetic concentrate assaying 66.1 wt.% Fe with a recovery rate of 91.2% was achieved from an Anshan-type carbonate-bearing fine iron ore assaying 42.0 wt.% Fe. The XRD, VSM, and optical microscopy analyses revealed that the siderite was successfully converted to magnetite by roasting. Some coarse hematite particles were difficult to reduce to magnetite completely; however, these generated magnetite particles with a fine hematite core could also be effectively recovered by magnetic separation after liberation from gangue minerals due to their strong magnetism. INTRODUCTION Magnetizing roasting followed by low-intensity magnetic separation has been considered as an effective solution, both technologically and economically, when upgrading refractory iron ores (Zhang et al., 2012; Peng et al., 2012; Li and Zhu, 2012). According to the type of roasting reactor, the magnetization roasting can be divided into shaft furnace roasting, rotary kiln roasting, and fluidized bed roasting (Zhu and Li, 2014).Shaft furnace magnetization roasting system is mainly composed of heating and reduction processes. The hematite ore is first heated to 700~800 °C in the heating zone, then falls into reduction zone where the weakly magnetic hematite is reduced to magnetite by coke oven gas at 550~600 °C (Yan et al., 2012). However, several years of engineering practices indicate that the shaft furnace can only process the hematite ores with a granularity of 15 ~75 mm, and the shaft furnace roasting is also characterized by heterogeneity of roasted product. Hence, the shaft furnace magnetization roasting technology is gradually replaced by high-gradient magnetic separation with the development of high-gradient magnetic separator. The rotary kiln generally handles the hematite ores with a grain size of less than 30 mm (Zhu and Li, 2014), however the formation of clinker ring in the rotary kiln will affect the yield of iron resource. In the fluidized bed furnace, the hematite ore is shaken up by an upward current of gas which maintains the individual particles in suspension (Yu et al., 2018). The precise adjustment of the gas velocity to the particle size and the specific weight of the hematite ore, make it possible to generate a floating mixture of gas and solids which behaves almost like a liquid (Yu et al., 2017a). The process is reported to have the following advantages over the other roasting techniques: ease of control due to absence of moving parts within the reactor, homogeneity of roasted products, ability to handle fine particles, and high efficiency of heat transfer and mass transfer (Li et al., 2015; Yu et al., 2017b). However, the simultaneous heating and reductive magnetization of hematite ore occur at the same place in the conventional fluidized bed reactor. Therefore, the reductive atmosphere, as well as the safety and stability of anti-explosion are hard to be controlled. Besides, the roasting temperature for conventional fluidized bed furnace is usually up to 950~1150 °C (Liu et al., 2017). Thus, the formation of clinker ring caused by high temperature will affect the operating efficiency."

Jan 1, 2018

By Yuqing Feng, Ping Fang, Dezhou Wei, Zichuan Guan, Shuling Gao, Baoyu Cui

"Air core, as an inevitable phenomenon of rotational flow field inside hydrocyclone, has a major impact on hydrocyclone’s separation characteristics. The air core formation process, its structural features and its influencing factors were investigated systematically in this paper. Numerical study on the air core of a f50 mm hydrocyclone was carried out using a commercial computational fluid dynamics (CFD) modelling software package ANSYS/Fluent with the selection of Reynolds Stress Model (RSM) for the turbulence model and Volume of Fluid (VOF) for capturing the air-liquid interface. Physical experiments were conducted under the same geometry and operation conditions and the particle image velocimetry (PIV) technology was used to measure the liquid flow. The CFD results are compared with the experimental measurement with good agreement demonstrated. The air core was formed generally at around 0.7 s, air outsides of the air core was eliminated completely after 1.7 s. The centreline axial velocities and the water blocking hydrocyclone simulations showed that air of the air core entered the hydrocyclone from the underflow area and exhausted from the overflow area, but there was also some air flowing into the air core from the overflow area. The largest swing of the air core occurred on the top of the underflow pipe, and a protuberance similar to the shape of Adam’s apple appeared when the air entered the vortex finder. CFD simulation results also showed that the air core diameter was decided by axial position and parameters of hydrocyclone. The structural parameters have more effects on the air core diameter than the operational parameters."

Jan 1, 2014

By P. Yu, L. X. Liu

"A mechanistic model for tumbling mills was developed during PhD studies at the JKMRC. The concept was presented at the IMPC of 2014, followed by progress in a sub-process of the model presented at the IMPC of 2016. Additionally, a number of papers on the sub-models and breakage function have been published. This paper provides a consolidated summary of the outcomes and status of the model. The overall model structure is presented along with the sub-models such as appearance functions, breakage rate functions, energy distribution, transport, and multicomponent grinding interaction model. The strengths and capabilities of the model structure as achieved to date are presented. The gaps in knowledge and sub-processes are also presented, providing a guide to the areas that require further research and development. It is proposed that the approach developed in this paper provides a structure that can accommodate future mechanistic, dynamic mill model evolution that can incorporate the latest research outcomes and provide a platform to test modelling improvements. This can assist in substantially improving the predictive mill modelling capability in the industry, the importance of which should not be underestimated for this workhorse of mineral processing.INTRODUCTION Grinding is almost the largest single energy-consuming process in the mineral processing industry, which was estimated that about 0.2% of global, and 1.3% of Australia’s electricity is consumed by comminution of gold and copper ores (Ballantyne and Powell, 2014). Although there are some relatively new grinding mills, such as stirred mills, vibrating mills and HPGRs (High-Pressure Grinding Rolls), etc., tumbling mills, as the traditional grinding facilities, are more extensively used."

Jan 1, 2018