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By R. ?. Sherembayeva, ?. ?. ?uktybayeva, ?. B. Rakhimbekova, N. ?. ?m?rova

"Studying the interaction of the phosphorus-containing flotation reagent with the components of the flotation system ""liquid-gas-solid"" during flotation of non-ferrous metal ores allows regulating the enrichment process. The phosphorus-containing reagent-collector anabasinium-O,O-dimethyl-thiophosphate has beensynthesized under laboratory conditions and the concentrated aqueous solution of anabasin hydrochloride and the 40% solution of sodium hydroxide have been used as the raw material. The phosphorus-containing reagent has been obtained by interaction of the anabasine base, sulfur and dimethyl phosphite, due to sulfur and nitrogen atoms it can form complex compounds with heavy metal ions.Studying flotation of copper-sulfide ore of the Sayak field with the use of the phosphorus-containing reagent-collector anabasinium has been performed in the open and closed cycles. The degree of ore grinding was 60- 62% of the class -0.074 mm. There has been established the dependence of the ore flotation parameters on: a) pH of the pulp; b) the consumption of the reagent-collector anabasinium.The effect of the pulp pH on the technological parameters of copper ore flotation has been carried out with a reagent regulator that increases the difference in the surface properties of the minerals to be separated.There has been used lime as the regulator of the medium, the consumption of which varied from 750 to 1500 g/t; the consumption of the reagent-collector anabasinium was 10, 15, 20 and 25 g/t.It has been found that when flotation of copper ore without the use of lime at pH equal to 7.8 and at the reagent consumption, g/t: anabasinium - 25, T-92 - 55, copper recovery in the concentrate is 92.72%, the quality of concentrate is 7, 1%.In flotation according to the factory mode (the consumption of xanthate is 44 g/t, T-92 is 55 g/t, pH = 7.8 (without lime)) of copper ore, copper recovery in the concentrate is 87.38%, the concentrate quality is 7, 97%, with reducing the xanthate consumption to 25 g/t copper recovery is reduced to 83.39%, the quality of the concentrate is up to 6.69%.In the experiments using the factory reagent mode in the closed cycle, with the xanthate mass consumption of 44 g/t, T-92 blowing agent of 55 g/t, the third recleaning concentrate contained 19.13% copper with recovery of 86.89%.Using a phosphorus-containing reagent instead of xanthate with the same flow rate, the third recleaning concentrate with the mass fraction of copper of 19.82% has beenobtained with recovery of 87.77%."

Jan 1, 2018

By M. Canbazoglu

In this study, optimum sulphuric acid leaching parameters of zinc and other valuable metals from two different waelz clinker samples were researched. Origins of the samples are electric arc furnace dust and original non-sulphite zinc ore waelz clinkers. The main zinc mineral determined as zincite in these samples. Collective dissolution of zinc and other valuable metals in waelz clinkers can easily achieved by sulphuric acid leaching of them. 96% of zinc can be dissolved at 80 ºC, 60 g/L sulphuric acid concentration, 60 min. leaching time and 1/5 solid/liquid ratio. Almost 90% of Cd, Cu and Co in clinker dissolved at these conditions while dissolution of Fe was almost 20%. The consumed acid amount for dissolved per ton of zinc is approximately 1.7 tons at these conditions.

Jan 1, 2014

By Wu Tao, Lu Shijie, Xia Xiaoou, Zhang Ming

The impeller and stator are the most important components that can significantly influence the performance of flotation cells directly. The performance of the impeller and stator of KYF flotation cell is revealed by CFD (Computational Fluid Dynamic) simulation in this paper. A method of obtaining the circulation volume is proposed. The circulation volume is proportional to third power of impeller diameter. And the circulation volume increases linearly with the increasing of the speed. CFD simulation can draw the conclusions that there is a proportional relationship between power consumption, third power of speed and fifth power of impeller diameter. CFD prediction results agree with the theoretical formula. The difference between the forward and backward impeller is analysed in the paper. The circulation volume of the backward impeller is obviously larger than that of the forward impeller under the same condition, but power consumption of the backward impeller is lower. It is demonstrated that the impeller and stator system of KYF flotation cell is an efficient and reasonable stirring mechanism. CFD simulation could be reliably used in flotation cell design and optimization.

Jan 1, 2014

By Érica Linhares, Anderson Silveira Lopes, Aline Costa

In the production units of ferromanganese alloys wastewater are generated. They mainly arise from gutters of drainage water from warehouse of raw material (manganese ore, reducing agents and other), product and slag. This wastewater, in general, may contain particles that will suffer difficulty to naturally decant, giving the water turbidity and color characteristics. Thus, this study aims to characterize the effluent, the treated water and the sludge from the sedimentation tank from the one main Brazilian plant. The investigated characteristics were: turbidity, total solids (TS), suspended solids (SS), dissolved solids (DS), pH, Eh, COD (chemical oxygen demand), residue classification and chemical analysis by ICP - OES. The turbidity before treatment was 417 NTU and after passing through the tank, 44 NTU, a figure slightly higher than the emission standards for Class 1 regulated by the Brazilian environmental legislation in force. The values for TS, SS and DS of the effluent were 225, 114.3 and 110 mg/L, respectively. For the treated water the values were 93, 48.3 and 45 mg/L for TS, SS and DS, respectively. The sedimentation process was able to reduce by 21 % of the COD. In the test of loss on ignition (LOI) from the tank bottom sludge were observed losses of 29.35 %, while the volatile analysis found 20.70 % of volatiles in the sample. It was determined that the concentrations of Al, Fe, Mn and S are, respectively, 0.1875 mg.L-1, 0.3071 mg.L-1, 0,789 mg l-1 and 0.00828 mg.L-1, values above the maximum allowed by law. Based on the analysis of X-ray diffraction, the identified minerals in the sludge were quartz, muscovite, kaolinite, calcite and albite.

Jan 1, 2014

By David I. Verrelli, Boris Albijanic

"Froth flotation is an exceedingly complex physicochemical process. The convenience of distilling much of the complexity of the bubble-particle interactions into a single parameter has led to the continuing popularity of the classical ‘induction time’ to quantify the threshold for bubble-particle attachment to occur. Despite this popularity and the simplicity of the concept, there is no single universal method of evaluating the induction period. In this paper, we begin with a critical review of the available techniques for estimating the induction period. These are: back-calculation from experimental (micro) flotation tests; pushing a particle toward a stationary bubble (or vice versa) using an atomic force microscope (AFM); pushing a bubble toward a stationary bed of particles in the ‘Induction Timer’; pushing a bubble toward a stationary solid surface using the ‘integrated thin film drainage apparatus’ (ITFDA); and dropping particles onto a submerged stationary bubble using the ‘Milli-Timer’ device. Each one of these methods has advantages and disadvantages, and the best choice depends on the application. In the experimental section, we present quantitative comparison of the induction periods estimated using two different techniques, namely the Induction Timer and the Milli-Timer. The same particles were tested in each device, under the same conditions. It was found that by tuning the operation of the particle pick-up device, similar estimates of induction period could be obtained to the estimates made by direct observation with the Milli-Timer. In the former device a bubble is driven toward a particle bed at a controlled rate, whereas in the latter a particle’s motion is governed by the hydrodynamics. The potential to match these presents an intriguing prospect for better understanding the bubble-particle interaction, and the possibility to ‘calibrate’ the simpler Induction Timer against direct observations."

Jan 1, 2014

By Ghislain Bournival, Seher Ata, Yesenia Saavedra Moreno

"In froth flotation, frothers are commonly added to the pulp to modify the interfacial properties of bubbles. These properties may be modelled using commercial software packages. The volume of fluid (VOF) method was used to track the interface motion during the post-rupture oscillation of the newly formed bubble. The aim of this research was to provide an insight into the modelling of viscoelastic phenomena through the coalescence dynamics of two bubbles in solutions of various surface tensions using a three-dimensional computational study. Different surface tensions were used to simulate changes in methyl isobutyl carbinol (MIBC) concentration. The computational results were evaluated by comparing the oscillatory motion of the newly formed bubble for the different MIBC concentrations. For known MIBC concentrations, the deviations of the computational damping constants from the experiments were quantified, revealing possible deviations in the VOF surface tension model. In addition, the analysis provided insight into the flow patterns of the fluids and the effect of frother concentration on the velocity magnitude in the liquid and air phases. This analysis provided a further understanding of coalescence dynamic and post-rupture oscillation in froth flotation. Such a process is believed to affect the stability of particles at the interface due to the release of surface energy when the bubble surface is reduced.INTRODUCTIONIn froth flotation, bubble coalescence is an important phenomenon that is highly dependent on the interfacial properties of the liquid film between bubbles. It is known that the frother adsorption at the liquid-air interface changes the interfacial properties, resulting in an increase of surface elasticity and reduction of surface energy (Pugh, 2016). However, in a two-phase system, it is the frother type, concentration, frother molecule conformation at the interface and viscoelasticity properties that dictate film stability (Pugh, 2016). The viscoelasticity phenomena can be explained in terms of surface viscosity, which quantifies the energy dissipation at the interface and surface elasticity that represents the energy absorbed at the interface as result of bubble oscillation (Pugh, 2016). In the case of systems stabilized by nonionic frothers, it has been shown that surface forces alone do not account for film stability, but the viscoelasticity represents the ability to damp external disturbances in the thin film separating the bubbles and prevent coalescence (Santini et al., 2007)."

Jan 1, 2018

By Komar Kawatra, Joseph Halt

"Bentonite clay has been the traditional binder for iron ore pellets. However, bentonite increases pellets’ silica contents and is expensive. Researchers have proposed lowering bentonite doses by mixing it with other common binders. These mixtures may only be successful if the fundamental bonding mechanisms are understood. For example, what happens when bentonite (physical bonding) is mixed with fly-ash (chemical bonding)? What happens when bentonite is mixed with cornstarch (physical bonding)? In this paper, experiments are described where bentonite was mixed with various ratios of cornstarch and fly-ash, and pellets were agglomerated using 0.66 % w/w binder. Ca(OH)2 and CaCl2 were added as activator and accelerator, respectively, to the bentonite-fly ash mixture. Curves of pellet dry strength vs. bentonite-starch ratio were linear, suggesting the physical-physical bonding mechanisms were compatible - acceptable strengths (> 22 N) were produced at all bentonite-to-starch ratios. This was contrary to bentonite-fly ash mixtures, which displayed dry strength curves with a noticeable minimum due to competing binding mechanisms. Bentonite alone and fly ash alone produced acceptable strengths (> 22 N), but their mixtures resulted in weak pellets. Due to the positive results using cornstarch (CS) binders, the effects of CS solubility in water were investigated using two CS with high and low solubility (60 and 7.5 %). CS was premixed with bentonite at various ratios (0, 20, 40, 60, 80, 100 %). Pellets were agglomerated using 0.66 % w/w binder. The dry strength of pellets ranged from 50-300 N using the high solubility CS mixtures, and from 50-85 N using the low solubility CS mixtures. Fired strengths exceeded 2200 N/pellet at all bentonite-cornstarch ratios. This research showed that cornstarch solubility is an important factor in determining its effectiveness as a binder for iron ore concentrates, but significant work is still necessary before it can be used as a bentonite replacement."

Jan 1, 2014

By D. Pienaar, B. McFadzean, T. Jordaan

"Dithiophosphate (DTP) collectors have the lowest affinity for sulfide mineral surfaces compared to other common sulfide mineral collectors, such as xanthates and dithiocarbamates. In some cases it has been found that DTP does not adsorb onto the mineral surface at all and yet increases in recoveries and grades are noticed with the addition of DTP. Many studies have investigated the interactive effects of collector mixtures. However, there have been relatively few studies on the interactive effects between frother molecules and collectors. This study investigates the interactions between different types of frothers and sodium diethyl dithiophosphate.The study found that there were large increases in pyrite and galena microflotation recoveries at both pH4 and pH9 when DTP was mixed with small amounts of frother at a constant bubble size, showing that these increases were neither mineral-specific nor pH-specific. The same effect was not present when xanthate was used as a collector. The increases in recovery when using the DTP-frother mixture were similar irrespective of the type of alcohol or polypropylene glycol frother that was used. In an attempt to distinguish the mechanism of enhanced flotation recovery, various supplementary experiments were performed. It was found through adsorption experiments that no DTP was adsorbing on to the mineral surface. Therefore, interactions at the air-water interface were performed. Surface tension and critical coalescence concentration tests showed that, while DTP is a weak surfactant at the air-water interface, it does not have a synergistic effect in the presence of frother. DTP-frother mixtures do, however, show interactions in the froth phase, indicating an interaction in the thin films. It is proposed that there is a DTP-frother interaction on the bubble surface that enhances the rate of film thinning at the 3-phase bubble-particle contact."

Jan 1, 2018

By S. Mitra1

"This study aims to investigate coarse particle detachment mechanisms (particle diameter > 150 ?m) utilising both experimental and numerical technique. Two mechanisms were studied – (i) interactions of bubbleparticle (BP) aggregate with vortices and (ii) coalescence of bubble-particle aggregates. On the first mechanism, interaction behaviour of coherent vortex structures with a BP aggregate (bubble diameter db = 3 mm, particle diameter dp = 0.3 mm) was studied using a CFD model in the Reynolds number range of 100 to 1000. Effect of surface hydrophobicity on the BP stability was examined using a range of contact angle boundary conditions. To address the second mechanism, interactions of bubble-particle aggregate (db ~ 4 mm, dp ~ 0.4 mm) with both free gas-liquid interface and individual bubbles were investigated using high speed imaging. Both rebound and coalescence outcomes were observed to be responsible for BP instability leading to particle detachment.INTRODUCTIONIt is widely known that flotation process performs excellent mineral recovery for base metal ore particles that are typically in the range of ~ 20 to 150 µm in diameter (Jameson, 2010). More specifically, higher recoveries are usually reported for particles in the size range of ~20 to 70 µm while outside this spectrum, generally the recovery diminishes significantly. It would be highly desirable to improve the recovery of particles at the coarse end of the flotation size range spectrum which has significant economic benefit (Jameson, 2010). However, it is essential that insights to particle detachment phenomenon, the primary impediment in coarse particle flotation caused by the underlying hydrodynamic factors are first obtained at a greater depth.In an ideal quiescent liquid medium, due to inertia, coarse particles deviate substantially from the fluid streamlines and collision efficiency with bubbles decreases which can only be augmented by increasing turbulence level in the medium sufficiently to make random physical contacts with bubbles. Nonetheless, even if successful contacts are made, it is difficult for these large particles to remain attached to bubbles in a turbulent shear flow environment. There are two major mechanisms postulated for particle detachment – interaction of turbulent flow structures (eddies) with BP aggregate and coalescence among surrounding aggregates. Earlier work of Schulze (1982) theorised a vortex acceleration component to characterise turbulence effect on BP aggregate instability in flotation machines. Wang et al. (2015) investigated bubble detachment behaviour from a stationary particle in a nearly homogeneous and isotropic flow field. Using PIV (particle image velocimetry), it was shown that the local maximum energy dissipation rate for the case of bubble detachment was significantly higher than the no detachment case, and was also higher than the critical value for bubble detachment calculated using Schulze’ theory (Schulze, 1982). Later, Wang et al. (2017) also visualised the BP aggregate instability in a cavity flow leading to particle detachment which was attributed to bubble coalescence, bubble surface oscillation and particle deceleration phenomena."

Jan 1, 2018

By Alexander E. Sobolev

The kinetics of oxidative dissolution of lead sulfide in solutions of nitric acid and sodium hypochlorite was studied using the rotating disk method and the factor experiment design. The dependences of the PbS dissolution rate on concentration of oxidant (HNO3 or NaOCl), temperature, disk rotation frequency, and duration of interaction were determined. The adequate kinetic models allowing calculating the specific dissolution rate at any combination of values of the influencing factors were obtained. As a result of the complex analysis of kinetic parameters, the modes of the each process proceeding were established, their macromechanisms were determined, and the limiting stages of the oxidative dissolution processes were revealed. The dissolution kinetics of lead sulfide in solutions of nitric acid was found to have several regimes. At HNO3 concentrations below 0.5 mol/L, the process proceeds in a mixed mode close to a diffusion-controlled. It is caused by low oxidative activity of HNO3 and considerable diffusional diffuculties at this acid concentration range. At the nitric acid concentrations more than 0.5 mol/L and less than 6.0 mol/L, the process was found to be kinetically controlled. The limiting stage of the interaction is the surface chemical reaction. The observed relatively high order of the dissolution rate with respect to the concentration of HNO3 was explained by the autocatalytic action of the acid reduction products. At nitric acid concentrations exceeding 6 mol/L, the process proceeds in a mixed mode close to a diffusion-controlled, and the dissolution rate sharply decreased that was explained by a decrease in the solubility of reaction products. When lead sulfide is dissolved in sodium hypochlorite solutions, at first time the amount of PbS transferred into solution remains close to zero. Gradually, as time goes, this amount begins to increase sharply. The dissolution rate rises and reaches the maximum value, further remaining constant. At the steady-state regime, the dissolution rate is independent of the duration of interaction and disk rotation frequency. The process was found to be kinetically controlled. The limiting stage is likely to be chemical reaction on the surface of solid lead sulfide. The obtained kinetic characteristics enlarge the database on hydrochemical oxidation kinetics of sulfides and can be used for the elaboration of the recommendations for the effective comprehensive exploitation of lead-bearing ores and concentrates. Keywords: lead sulfide, nitric acid, sodium hypochlorite, hydrochemical oxidation, dissolution kinetics

Sep 1, 2012

By John Ralston

"Interfacial chemistry plays a pivotal role in bubble-particle capture, for it controls whether or not attachment occurs. Surface heterogeneity, degree of surface hydrophobicity, bubble nucleation and related phenomena influence the stability of the aqueous wetting film between a particle and an approaching bubble. The latter must be unstable if capture is to occur. Various techniques that may be used to quantify this interfacial, chemistry-dominated behaviour, are described.The efficient capture of specific particles by rising bubbles and the delicate control of interfacial chemistry that leads to selective capture are central issues in froth flotation. For efficient capture to occur between a particle and a bubble, they must undergo a close encounter, a collision process dominated by hydrodynamics. Should this encounter bring the particle and bubble within the range of attractive forces, the intervening liquid film between the bubble and the particle will drain, leading to a critical thickness at which rupture occurs. The liquid-vapour interface then retreats over the solid particle surface until a stable wetting perimeter is established. The particle and bubble are then joined after this attachment process. The particle may only be dislodged from this state if it is supplied with sufficient kinetic energy to exceed the detachment energy in this detachment process. These various events are now well documented and may be followed using high-speed videomicroscopy (Schulze, 1984; Nguyen et al., 2001).The process of collision can now be described quantitatively for single bubbles colliding with bubbles under various flow regimes (Dai et al., 1998) and appropriate scale up is possible for multiple bubble particle collisions occurring under turbulent conditions (Pyke et al., 2002). In this paper we will be concerned with the role of interfacial chemistry and how this influences the attachment process."

Jan 1, 2003

By M. M. Fan

In Florida?s phosphate industrial practice, the most favorable upper size limit of froth flotation is 1.18 mm which corresponds to particle weight of about 2.8 mg. Conventional froth flotation is not efficient in upgrading coarse particles (+0.425-1.18 mm). A limited number of studies have been devoted to understanding and improving coarse particle flotation. We have shown that the coarse particle flotation performance can be significantly improved by the presence of picobubbles generated by hydrodynamic cavitation. In this study, the size of picobubbles produced under certain hydrodynamic conditions was measured by a laser particle size analyzer. A size-by-size flotation performance analysis of coarse phosphate froth flotation in the presence of picobubbles is conducted in terms of flotation kinetics, selectivity and recovery. It was found that picobubbles doubled the flota-tion rate, increased the P2O5 recovery more significantly for +0.85-1.18 mm particles than +0.425- 0.6 mm and +0.60-0.85 mm particles. At a given acid insolubles (A.I.) rejection, the presence of picobubbles increased the P2O5 recovery by up to about 25%.

Jan 1, 2014

By Mike Daniel, Eric Wang

"Several new large copper and gold concentrators have been built and commissioned around the world in the past five to eight years. The success of the ramp-up from these very large concentrators has varied. CITIC SMCC Process Technology was engaged to assist some of these mines by gaining a better understanding of the factors that influence throughput capacity. As such, site-specific throughput forecast models that are influenced by SAG mill performance were developed. The forecast models are easy to interpret and modify and can greatly assist the mine management to make predictions and informed decisions for a range of site improvements. The models investigate the influence of SAG mill performance with respect to ore competency, derived from SMC Test® via the measured DWi model parameter. In some cases the benefits of blasting and from fine tuning milling operations are already incorporated into the "site-specific" forecast models. The methodology follows rigorous plant data analysis that is analogous to a "Mine-to-Mill®" optimisation project. The CITIC-SMCC model validation includes extensive data collection, which includes drill core analysis, ore characterisation and comprehensive comminution circuit operational data to assess the limitations within the comminution circuit within the operating mine. The results and models may be used to define the operating base lines of the processing areas and identify improvement opportunities upstream and downstream of the comminution circuit. The predictive capability of the models use logged production data and has enabled the user to differentiate between alternative circuit configuration options and identify optimum operating conditions. This approach minimises the ongoing requirement for costly plant surveys. The improvement strategy for each site, included the ongoing measurement of grindability, rock strength and via the Bond and SMC Test® respectively. Some commentary as to what other practitioners do with input data and their models is also presented as this highlights some of their shortcomings relative to the CITIC-SMCC methods."

Jan 1, 2014

By Adam Jordens, Olga Kuzmina, Christopher Marion, Kristian Waters

"In order to meet the growing demand for non-Chinese rare earth suppliers many new rare earth (RE) mineral deposits are currently under development, however these deposits typically include many minerals for which there is little processing information available. One of these deposits is the Nechalacho deposit located in the North West Territories of Canada. This deposit contains multiple RE minerals including bastnäsite, zircon, fergusonite, allanite and monazite. The work presented here investigates the use of different classes of flotation collectors (carboxylic acids, hydroxamic acids, phosphoric acids) typically used in RE mineral flotation to float the Nechalacho ore directly. Flotation tests are also conducted as the final step in a beneficiation process incorporating centrifugal gravity concentration and magnetic separation. This combination of centrifugal gravity concentration and magnetic separation rejects low specific gravity gangue minerals such as K-feldspar and plagioclase and concentrates high specific gravity minerals such as magnetite and hematite. The removal of low specific gravity gangue helps to improve flotation and the removal of ferromagnetic iron oxides is important prior to flotation using certain chelating collectors."

Jan 1, 2014

By S. M. Bradshaw, C. Dorfling, F. Ngandu

"Selenium removal and platinum group metal (PGM) recovery from copper sulfate leach solutions form an integral part of platinum producers’ base metal refinery operations. Recent studies found that substantially higher PGM recoveries can be achieved if excess thiourea instead of sulfurous acid is used as precipitation reagent; however, the impact of the proposed process on downstream processes was unknown. The objective of the current study was therefore to investigate the effects that excess thiourea and residual selenium present in the rich copper sulfate electrolyte have on copper electrowinning. This was achieved by performing cyclic voltammetry tests using a platinum rotating disk as working electrode, a graphite auxiliary electrode and a saturated calomel reference electrode. A synthetic copper sulfate electrolyte containing 0.01 M Cu2+, 1 M H2SO4 and varying amounts of selenium (20 – 150 mg/L) and thiourea (10 mg/L and 100 – 300 % excess) was used. The results obtained have shown that both thiourea and selenium interact with the cupric ion cathodic reduction reaction. Thiourea polarized the working electrode and lowered the efficiency of the cupric reduction reaction. Tests on the solutions with high selenium concentration showed simultaneous reduction of copper and selenium, which led to copper selenide formation. Nodule formation on the deposit surface also became significant at higher selenium concentrations. Based on these results, it was concluded that precipitation of PGMs from the copper sulfate solution with excess thiourea is not feasible due to the detrimental effect on downstream electrowinning operations.INTRODUCTION During the high pressure oxidative leaching stage in a typical base metal refinery (BMR) circuit, selenium, tellurium and some platinum group metals (PGMs) are dissolved along with the desired copper ions. The impurities (selenium and tellurium) may pass to the copper electrowinning circuit where it can result in the formation of nodular copper electrodeposits or reduced current efficiency. The presence of PGMs in solution, on the other hand, increases the precious metal inventory and potential losses of the operation. Currently, sulfurous acid is widely used for selenium and tellurium precipitation from copper sulfate leach solutions. Sulfurous acid is capable of reducing cupric ions to cuprous ions; the generated cuprous ions then react with Se4+ and Se6+ to precipitate selenium as a copper selenide (Bello, Dorfling, 2014). Recent studies have, however, proposed the use of excess thiourea as a precipitating agent for the removal of selenium and tellurium; it has the advantage of improved PGM recovery in the Se/Te precipitation step (Lottering, Eksteen et al., 2012; Mulwanda, Dorfling, 2015)."

Jan 1, 2018

By A. Buchanan, M. Mirnezami, A. L. Restrepo, J. A. Finch, M. S. Hashemi

Settling rate studies on slurries from Cu/Zn flotation plants occasionally revealed two aggregation maxima at pH 8-10 and 10-12. From measurements on sphalerite and silica suspensions the double maxima were replicated by Zn ions (pH 8-10) and Mg ions (pH 10-12) corresponding to the presence of zinc hydroxide and magnesium hydroxide, respectively. A combination of chemical and electrostatic bridging by the hydroxides is considered to be the aggregation mechanism.

Jan 1, 2003

By Brochot. Stephane, Manuel Gonzalez Fernandez

"HPGR (High-Pressure Grinding Rolls) is widely used today for grinding of various kinds of ores such as iron ore or base and precious metal ores. It can be used as first stage of grinding replacing tertiary crusher and SAG mill, but also as regrinding stage to enhance mineral liberation. In addition to better energy efficiency, the advantage of HPGR is to produce much more internal particle fractures allowing faster leaching as it has been demonstrated for some gold ores. This grinding mode of compression and fracture generation also promotes mineral liberation without overgrinding. Mineral processing modelling and simulation associated to detailed ore characterization constitute a powerful tool for plant design and optimization. The mathematical models of the units of operations (grinding and separation) have to reproduce the mineral deportment for which the mineral liberation plays a central role. The present paper is focused on the HPGR modelling with the objective of plant optimization or advanced design from pilot plant tests. The traditional approach of the population balance linked to the energy dissipation and the residence time distribution is generalized in association with a mineral liberation model. The effect of the specific HPGR breakage matrix and grinding function on the mineral liberation rate is discussed and compared to the tumbling mill. The implementation of this mathematical model into a plant simulation tool is illustrated by the example of the optimization of an iron ore concentrator."

Jan 1, 2014

By Lutz Rolf, Halit Z. Kuyumcu, Salas Cazón. Milton A.

Aim of experimental investigations was the mathematical description of the abrasion process running with a single particle stress. This is on the one hand the basis for the physical interpretation of the process, on the other hand the base for the simulation of abrasion processes carried out in technical scale. With this investigation for the first time the influence of the particle shape changing with increasing abrasion progress was quantitatively described. This influence affects itself particularly strongly on break-fresh particles up to an abrasion degree of approximately 10 to 20%. This is for the description of technical processes the most interesting area.

Jan 1, 2003

By Bulelwa Ndlovu, Saeed Farrokhpay, Dee Bradshaw

The effects of phyllosilicate minerals on the flotation performance and froth stability of a copper ore was investigated. It was found that various phyllosilicate minerals affect the copper recovery differently however they all caused the flotation grade to be reduced. The effect of different phyllosilicate minerals on the froth stability followed the order of talc >> montmorillonite > muscovite > kaolinite > illite. The results demonstrated that there could be a relationship between the deleterious effect of phyllosilicate minerals on the flotation and froth stability. Talc and montmorillonite have both shown the highest effect on the flotation recovery and grade as well as froth stability. On the other hand, illite has the least effect on the both flotation performance and froth stability. Kaolinite and muscovite also affected the copper flotation grade (but not the recovery) while they also affected the froth stability. Therefore it is possible to control the flotation performance when phyllosilicate minerals are present via monitoring and controlling froth stability which needs to be investigated further.

Jan 1, 2014

By Kaiwen Liu

Activated carbon is widely used in the removal of organic and/or inorganic contaminants from waste water due to its high surface area, porous structure, and specific surface reactivity. However, in practical applications, it is difficult to recover the activated carbon completely by screening or classification. In this project,we prepared a magnetic form of activated carbon (magnetic activated carbon or M-AC) by precipitation of iron oxides on the surface of activated carbon. The M-AC can be easily separated from effluents by applying an external magnetic field, thus it can be recycled and regenerated for reuse. M-AC was characterized by X-ray diffraction (XRD), specific surface area measurement, and scanning electron microscope (SEM).XRD results show that the major phase of coated iron oxides on activated carbon is magnetite (Fe3O4). The specific surface area of activated carbon was found to be reduced after the impregnation of magnetite particles on the surface. The SEM micrograph shows the aggregation of the iron oxides on the surface of activated carbon. M-ACwas found effective in removing DETA (diethylenetriamine) species and metal ions from solutions. Cu (II) with initial concentrations from 5 ppm to25 ppm in solution is removed by more than 99% with the addition of 0.1 wt.%ofM-AC. For the removal of 25 ppm DETA species from solution, an addition of 0.5 wt.% of M-AC is required due to the larger size of the DETA molecule. Moreover, M-AC showed a good loadingproperty for nickel and gold ions from solutions. M-ACshows a better adsorption capacityover activated carbon and its potential applications in carbon-in-pulp for gold leaching and waste water treatment. Keywords: magnetic activated carbon (M-AC),diethylenetriamine (DETA),metal ion,adsorption

Sep 1, 2012