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By Swati Mohanty

Spiral concentrator, which works on the principle of gravity separation, is widely used in the mineral industries for separation of solid particles based on the size and density. In the present study, CFD simulation of the flow profile on a laboratory scale spiral concentrator of height 2.29 m, pitch 0.435 m and width 0.17m was carried out. A single computational domain covering the entire spiral was considered. Volume-of-Fluid algorithm was used to track the interface and predict the flow profile. In the present study the Donor-Acceptor method was used for the calculation of volume fraction in the cell. Simulation results show that the velocity increases as the water flows down due to the convective force and gravitational force, but the viscous force acting in the opposite direction retards the flow. Thus the maximum velocity is attained at turn three at which the viscous force overpowers the other forces and further down the velocity decreases. Measured water depths along the radius of the spiral at various heights were compared with simulated depths, which were in good agreement. The simulated liquid phase velocity profile was used to carry out preliminary studies on the flow profile of solid particles of size 500 micron and densities 2600kg/m3 and 5100kg/m3, based on the Lagrangian model taking into consideration fluid-particle interaction.

Sep 1, 2012

By W. H. Cheung

Nickel and cobalt production relies heavily on the processing of nickel laterite ores; these ores contain the majority of known Ni and Co reserves, 80% and 90% ~ 95%, respectively. The Caron process is used to extract Ni and Co metals from low-grade nickel laterite ores (1% Ni and 0.1% Co). It involves selective reduction of NiO and CoO minerals followed by ammoniacal leaching. Despite low metal recoveries, this process continues to be technically and economically reliable and thus commercially important globally. However, keeping the Caron process cost-effective has been a challenge for industries because of increasing economic and environmental pressures. Although studies of the Caron process have been extensive, significant improvements in recoveries of industrial processes have not been forthcoming. Reported industrial metal recovery from high iron content ore is only 80% ~ 85% for Ni and only 40% ~ 45% for Co; recovery is even lower for ores rich in magnesium. The real difficulty here is that there is no complete understanding of and control over the complex series of reactions in the ore and in the leaching solution during processing. Achieving effective metal recoveries from the Caron will require control of the mineral transformations, which affect the activation of minerals by reduction. In this study, the effect of over-reduction was investigated, which superseded the effect of activation by lowering the activity of the minerals and thus metal dissolution. Reduction was carried out in a batch reduction apparatus with 1:1 and 1:2.5 CO/CO2 gas mixtures from temperatures of 500 ~ 700°C and residence times up to 60 minutes. The pre-reduced ores were leached using a standard ammoniacal leaching test. Thermodynamic analysis and possible effects of stable phase field on leaching was examined. The results suggest that control of over reduction effects are directly related to the mineral transformation and reduction conditions.

Jan 1, 2014

Calcium sulfate whiskers are considered to be a prosperous reinforced material in application due to their high mechanical properties. But the hydration occurs easily at moist atmosphere or in aqueous solution. The surface topographies of the calcium sulfate hemihydrate whiskers and the hydrates were analyzed by on-line observation and using XRD. The results indicated the transformation of the crystal type and shape of calcium sulfate hemihydrate whiskers and the reduction of whiskers? aspect ratio. The hydration process of the calcium sulfate hemihydrate whiskers and the effective parameters were further discussed based on FT-IR measurements. The conclusions were obtained that the hydration of calcium sulfate hemihydrate whiskers can be divided into the three phases, namely, initial hemihydration phase, dehydration phase, and coarsening, dissolving and the re-formation of calcium sulfate dehydrate crystal phase. In addition, it was found that in the hydration process of calcium sulfate hemihydrate whiskers the calcium sulfate dihydrate whiskers are formed at first and then converted into the calcium sulfate dihydrate with different crystal shapes, but in the hydration of gypsum hemihydrate the gypsum dihydrate is formed without transition products. The surface active site-calcium ion which has strong trend to react with H2O, the surface ?OH and the inner channels are considered to play important roles in the hydration process of calcium sulfate hemihydrate whiskers.

Jan 1, 2014

By James A. Finch

"Developed countries are in the midst of re-structuring education in minerals-related disciplines as raw materials, once vital to wealth generation, contribute progressively less to the economy. The changing circumstances mean institutions must justify mineral processing by new criteria. After considering what a mineral processor needs to know the ways to deliver are considered. Taking twenty graduates per year to illustrate, one institute could justify this number as a program in a department or school (of whatever grouping of disciplines). A strong research component would make the package additionally attractive. Divide among four institutions and mineral processing is best served in a research centre with delivery taking advantage of multi-centre and distance learning opportunities.INTRODUCTIONThis is one of five plenary lectures at the Congress. I may have preferred a technical subject, as that is what occupies most of my thinking hours, but it is reasonable as an academic that this topic should come to one of us. The fact the topic has not been high on my agenda may provide one advantage: that I can suggest directions free of pre-conceived notions, just as when reviewing the background to a technical article the temptation to select in support of one?s interpretations is resisted. The trick will be to add something new.One reading of the title seems to query whether mineral processing education has a future. (I will refrain at this juncture from defining mineral processing and assume for now we share an understanding of the term.) The proximity of natural and human resources led to the Industrial Revolution and the interaction continues to stimulate and sustain industrial and economic development in many parts of the world. The search for raw materials has historically played a key role in opening frontier areas, with undersea and outer space next. The reason is obvious: raw materials along with food and energy underpin society. Thus mining will remain part of human activity along with the need to pass on the knowledge and skills.What happens over time is resource relocation. Raw materials become exhausted in one area to be replaced by sources elsewhere; the demand for some materials lessens while growing for others. Educational institutions can find themselves with the wrong geography or with staff focussing on the wrong subjects. When this happens the restructuring produces much discussion. This is where we are in parts of the world. Japan, Western Europe and the United States are the prominent examples (Dowd, 1998; Flemings and Suresh, 2001; McDivitt, 2002). Mineral processing is becoming a series of courses in related disciplines: resource engineering, environment engineering or materials engineering. The start of the transition is evident in Canada and Australia, perhaps earlier than expected given the contribution of raw materials to their economies. A common backdrop in the developed countries is social pressure to reduce the impact of the ?untidy? aspects of life, and that includes mining. (This is not new: in classical times the mine face was the preserve of slaves and convicts.) These values are exportable, potentially affecting recruitment into mining schools everywhere."

Jan 1, 2003

By Al Cropp, Julie Hunt, Will Goodall, Ron Berry, Dee Bradshaw

Geometallurgy aids the understanding of ore body variability but has the most value if the data is easily available along the entire mining value chain. This requires cross-discipline communication and collaboration across traditional silos, and an organizational culture that encourages that to flourish. Data that are collected by the numerous groups (i.e. mining, geology, milling, processing, refining, smelting, marketing, environmental etc.) involved in the mining process may have relevance to other stakeholders; mineralogical and textural data for example has value to all these groups. Data required for modeling comminution or identifying acid potential from waste rock may already exist, however it needs to be made available to all the relevant stakeholders in the right format at the right time. As part of the GeM (AMIRA P843 & P843A) project the opportunity has been taken during the sponsor meetings, short courses, case studies etc. to ask the question: ‚What information do you want from further up the chain?? For example, to metallurgists ‚What information would you like from the geology group before the ore enters the mill?? The geology group may already have information important to mineral processing but not know it is of interest. This could, for example, be in the form of a geometallurgical drill core log that contains quantitative measured values. This paper focuses on the interaction between the mining, geology, mineral processing and environmental groups, using ore properties resulting from geological alteration to identify potential impacts throughout the mining process and discusses how a cross discipline approach can benefit all.

Jan 1, 2014

By M. Paymardi, A. Foroutan, T. P. Oladele, M. Abbaszadeh

"Reducing the amount of zinc and iron in lead concentrate is one of the important aspects of processing in lead and zinc flotation plants which results in improvement of lead concentrate quality and prevents zinc loss. In mineral flotation industries, lignin sulfonates are known for their depressant properties for both non-metallic and sulfide minerals such as pyrite and pyrrhotite.This paper investigates the effect of lignin sulfonate on flotation of galena, sphalerite and pyrite in sulfidic lead and zinc bearing ores. Batch flotation tests were carried out on a high pre-activated zinc samples. The feed contains 0.9% lead, 2.3% zinc and 7.5% iron. The dosage of all reagents such as sodium cyanide, zinc sulfate, ethyl xanthate and methyl isobutyl carbinol (MIBC) were kept constant for lead flotation step except calcium lignin sulfonate (CLS) that was varied between 0 and 80 gr/ton.Results for lead rougher concentrate showed that the grade of lead increased by 2.7% while the recovery decreased around 4 % at the highest dosage of CLS. Furthermore, zinc recovery decreased by 6.3% with no significant change in grade. Iron recovery in lead rougher concentrate decreased by 2.3 % while the grade changed around 1%. In sphalerite flotation step, CLS dosage was changed in the range of 0 to 80 gr/ton while the dosage of other reagents such as copper sulfate, lime, amil xanthate and MIBC were kept constant. In this step, no decreasing in grade and recovery of zinc was observed, while iron recovery decreased. It was suggested that CLS has a depression effect on sphalerite in conjunction with other zinc depressants such as zinc sulfate and sodium cyanide. CLS was further used in plant with non-pre-activated zinc minerals. Similar trends were observed in plant.INTRODUCTIONlead-zinc sulfide minerals play an important role in the production of lead and zinc metals in the mineral processing industry (Luo, Feng et al. 2016). Due to complexity of the lead-zinc ores mineralogy, in some situations, their flotation properties vary significantly from one deposit to another one even in itself (Bulatovic 2007)."

Jan 1, 2018

By Henrique Kahn, Daniel Uliana, Carina Ulsen, Guilherme Nery

"Gold has been a material in high demand since the dawn of humanity. After hundreds of years of exploitation, the increasingly search for gold occurs in lower grade deposits with greater extraction difficulty. Therefore, for maximum efficiency, deep knowledge of the characteristics of these minerals and their associations is crucial, which is acquired through an accurate and rigorous routine of process mineralogy and batch extraction tests. The industrial gold process extraction occurs by gravity concentration, sulphides flotation and cyanidation. For gravity concentration, it is fundamental to establish the proportion of free or coarse gold grains and its association to heavy minerals; regarding flotation, the most relevant data are the proportion of gold associated to sulphides and their liberation by the surface area; for cyanidation, it is crucial to evaluate gold accessibility and the kinetics of leaching. Thus, the characterization of gold associations and liberation is vital to establish the plant design, to optimize operating plants and to reduce gold losses. Our aim is the characterization of gold occurrence in low-grade Brazilian deposits with complex mineralogical assemblages to support processing flowchart definition and to predict metallurgical recoveries. Gold distribution in light and heavy minerals was evaluated by heavy liquid separation and the occurrence of gold in free or locked particles was carried out on heavy products by SEM-based automated image analysis using the MLA system. All the products of heavy liquid separation were cyanidated in head samples with different milling conditions to evaluate the reaction kinetics and maximum recovery."

Jan 1, 2014

By Ana C. C. Pacheco, Maurício L. Torem

"The aim of this work was the study of the effect of the type (Fe3+, Al3+ and Fe3+ and Al3+ mixture) and of the coprecipitant concentration on As5+ removal by ACF. Removal of As5+ using sodium dodecyl sulfate (SDS) as a collector was studied by Adsorbing Colloid Flotation (ACF) at laboratory scale. The morphology of the precipitate retained in the foam was analyzed by Scanning Electron Microscopy (SEM/EDS).In order to investigate the effect of the initial concentration of Fe3+ on As removal, sets of experiments were performed with a concentration of Fe3+ in the proper range of pH (5,0 – 6,0) previously observed in the coprecipitation tests. As removal improves significantly as the concentration of the coprecipitant agent increases from 60 mg.L-1 (77,4%) to 80 mg.L-1 (99,7%). This is probably due to the higher concentration of ferric hydroxide (Fe(OH)3) which provides a larger surface area available for adsorption of As. From the initial coprecipitant concentration of 80 mg.L-1, As removal has shown to be rather high (? 99,7%), with the maximum being (99,9%) by using a Fe3+ concentration of 160 mg.L-1. Therefore, for a maximum As removal, under these test conditions, the optimum concentration of Fe3+ is 160mg.L-1.This paper also shows the effect of the initial concentration of Al3+ on As removal at a suitable range of pH (7,0 – 8,0). A very significant increase on As removal was found to occur as the initial concentration of coprecipitant was increased from 60 mg.L-1 (35,7%) to 80 mg.L-1 (97,7%) and a decrease in As floatability (43,7% - 54,5%) was found to occur from that Al3+ concentration amount. Based upon those results, the optimum Al3+ concentration so as to remove As under these test conditions is 80 mg.L-1."

Jan 1, 2003

By H. Lieberwirth, M. Hesse

"Selective comminution (SC) is beneficial for the treatment of primary raw materials, especially if it is utilized in the pre-concentration process. Pre-concentration processes are applied in mineral processing to relieve subsequent processes and to achieve a higher efficiency. SC is also a promising method for the treatment of low-grade ores and waste dumps. With SC, various components can be separated such as valuable minerals from waste, ore from wall rock and different ore varieties within a deposit. SC is a property of a comminution system and leads either to a preferred crack propagation in one component (called preferential breakage) or to a preferred crack propagation along the grain boundaries (called interfacial breakage). SC results from different comminution behavior of various components in the feed material. For mechanical comminution, the preferential breakage seems to be the most important case of SC. Hereby SC generates only the difference in the particle size which can finally be used as a sorting parameter. A sorting process which uses SC depends on three parts: the feed material, the comminution machine and the separation machine. The feed material defines the potential for SC. Differences in properties like strength, toughness and density which are related to comminution are often used. The comminution machine has to exploit this potential. The extent of the exploitation can be influenced by the machine design, material and operational parameters. After SC, the various components are still combined in the product. So ultimately, a separation machine is needed. At preferential breakage, a simple screening machine can be used. The basics about SC will be presented at first. This contains relationships between material properties, the kind of loading in the comminution machine and the SC effect. These basics can be used for example to exploit a potential to SC for a pre-concentration step or to avoid the SC for a higher efficiency of subsequent processes. Based on recent investigations with impact load, the influence of the important parameters compressive strength, density, particle size and impact velocity to the SC will be shown, using examples of lead-zinc ore comminution and fluorspar processing."

Jan 1, 2018

By Tasuma Suzuki

Electrokinetic/permeable reactive barrier system is a promising in situ soil and ground water remediation technique to reduce toxic NO3- into less toxic NH4+. Using granular zero-valent iron (Fe0) as a reductant, the first objective of this study was to investigate the influence of the solid-liquid ratio and aqueouspHon NO3- reduction. The results obtained from a series of batch experiments showed that NO3- reduction was enhanced by either increasing solid-liquid ratio or decreasing aqueous pH. Based on insights obtained from batch experiments, the second objective of this study was set to design the remediation conditions of the electrokinetic/Fe0permeable reactive barrier system to maximize the NO3- reduction efficiency. Experimental results showed that the effectiveness of the system strongly depended on the Fe0 percentage in the reactive barrier, the pH in the anode reservoir, and the applied voltage, which were consistent with the results obtained from batch experiments. Under optimized treatment conditions, nearly 100 % NO3-was reduced into NH4+ in the permeable reactive barrier and collected in the cathode reservoir. Insights obtained from this study provided fundamental information on roles each of remediation design parameters plays, and will be useful to optimize the remediation conditions. Keywords: electrokinetic remediation, permeable reactive barrier, zero-valent iron, nitrate

Sep 1, 2012

By Zhou Yucai, Zhou Jing, Zhu Yimim

"In this article, research on the beneficiation process for a carbon containing copper-molybdenum deposit in Henan province has been carried out. The elemental composition, mineral composition and relative content, characteristics of embedded and symbiotic relationship, the forms of the copper-molybdenum particlesand their disseminated features, and particle size distribution have been worked out. Flotation behavior of copper-molybdenum mixed flotation and separate flotation in the systems of different collectors and depressants, and the influence of different flowsheets on the copper-molybdenum separation have been investigated by actual ore flotation tests, The separation problem of copper-molybdenum for a carbon-containing copper molybdenum ore has been solved.INTRODUCTION In this paper, technological mineralogy, small experiment of flotation recovery of copper Molybdenum ore, and expansion experiment of mineral recovery of copper Molybdenum ore are introduced. (1) The results of process mineralogyshow that the content of copper is 0.42%, molybdenum is 0.021% in the raw ore, they mainly exist in the form of sulfide, with low oxidation rate. (2) The results of flotation tests show that the combination of butyl xanthate and isopropyl ethylthionocarbamate reagents is effective collector of copper-molybdenum mixed flotation for carbon copper molybdenum, (3) When the grinding fineness is -0.074 mm taking 71%, and regrinding fineness is -0.038 mm taking 85%, the flowsheet of first copper-molybdenum mixed flotation and then regrinding rough concentrate and last separation flotation of copper and molybdenum was adopted, which realized the effective separation of copper and molybdenum for carbon-containing copper molybdenum ore. Good flotation indexes were gained with copper concentrate containing 20.96% copper and copper recovery 90.06%, and molybdenum concentrate containing 46.78% molybdenum with molybdenum recovery 72.68%. (4) The seven days average concentration index of scale-up the continuous dressing experiment is as follows, the copper content in copper concentrate is 20.16% and the recovery is 89.61%; the molybdenum content in molybdenum concentrate is 24.58% and the recovery rate is 74.09%."

Jan 1, 2018

By Felix M. Zhuravlev, Vitalij P. Lyalyuk

"While there is a large industry based on recovering platinum group metals (PGM) from complex sulphide ores containing Cu and Ni, there is little information on the thermodynamics of the matte phase formed on smelting the ore and in particular the behaviour of Pt in the matte.The equilibrium between metallic platinum and industrial mattes was studied in a series of experiments where a small quantity of matte (5g) and platinum foil of 150 µm thickness (0.5 g) were equilibrated in magnesia crucibles at 1400°C under conditions where the oxygen and sulphur partial pressures were controlled.The chemistries of the phases were determined from EDS analysis using a scanning electron microscope. Line scans were initially used to confirm that the foils had attained a uniform composition across their thickness. The composition of the matte was determined from analysis of an area of matte including the small metallic droplets and dendrites.The distribution of Pt in Cu-Fe-Ni mattes (Pt: 1.5 – 3%) and solid Pt alloys (Pt: 54 – 72%) was studied. For a matte of base composition 45%Fe, 11%Ni, 8% Cu, at a base temperature 1400°C, the following behaviour was observed for the Pt distribution ratio:Under the range of sulphur and oxygen pressure of this study (log pO2 from -15 to –12.2, log pS2 from – 4.6 to –2.2), the distribution ratio of Pt between matte and alloy was independent of the sulphur and oxygen pressure, having a value of 0.04.The Pt distribution ratio increased from 0.02 to 0.08 with temperature from 1340 to 1450 oC.For mattes where the proportions of Cu and Ni were kept constant, a slight decreasing trend was shown for the distribution ratio of Pt versus the iron content (37 to 53%) in the matte but was not confirmed because of experimental uncertainty."

Jan 1, 2003

By Georgios N. Anastassakis

"The depletion of the high-grade chromite ores and the inefficiency of the gravimetric methods to process fine particles has shifted the industrial and research interest from gravimetric separation methods to flotation. However, the response of the minerals to various flotation schemes is not clearly established. In this work, the physicochemical behavior of chromite and olivine is studied using a fatty acid collector.The minerals used were from Vourino area (Kozani, Northern Greece). Macroscopically pure samples of chromite and olivine were selected by hand picking, crushed and subsequently ground to the required size. Each sample was then submitted to panning and magnetic separation for the removal of impurities. The mineralogical and chemical analysis of the purified samples revealed the following: a) The purity of chromite was 95% while the minor constituent was mainly magnetite. Its chemical analysis was: 12.50% Fetot, 2.50% SiO2, 54,54% Cr2O3, 9.31% Al2O3, 0.47% CaO, 13.10% MgO. These analyses show that Cr3+ has been substituted by Fe3+ and Al3+ as well as Fe2+ has been significantly substituted by Mg2+. b) Forsterite is the main constituent of olivine either as pure forsterite (Mg2SiO4), which is the prevailing form, or as iron-forsterite [(Mg,Fe)2SiO4] in less amount. Chrysotile, which belongs to the serpentine group, was also detected at a percentage of 10-15%. The chemical analysis of olivine was: 36.90% SiO2, 0,53% Cr2O3, 7,43% Fe2O3, 0.72% Al2O3, 0.91% CaO, 47.00% MgO, 6.02% LOI.The electrokinetic behavior of the minerals was studied in a electrophoretic mass transport equipment Model 1202 of Micromeritics. The reagents used were sodium hexa-metaphosphate of commercial grade and sodium oleate."

Jan 1, 2003

By Steven Wright, Sharif Jahanshahi, Shouyi Sun

"While there is a large industry based on recovering platinum group metals (PGM) from complex sulphide ores containing Cu and Ni, there is little information on the thermodynamics of the matte phase formed on smelting the ore and in particular the behaviour of Pt in the matte.The equilibrium between metallic platinum and industrial mattes was studied in a series of experiments where a small quantity of matte (5g) and platinum foil of 150 µm thickness (0.5 g) were equilibrated in magnesia crucibles at 1400°C under conditions where the oxygen and sulphur partial pressures were controlled.The chemistries of the phases were determined from EDS analysis using a scanning electron microscope. Line scans were initially used to confirm that the foils had attained a uniform composition across their thickness. The composition of the matte was determined from analysis of an area of matte including the small metallic droplets and dendrites.The distribution of Pt in Cu-Fe-Ni mattes (Pt: 1.5 – 3%) and solid Pt alloys (Pt: 54 – 72%) was studied. For a matte of base composition 45%Fe, 11%Ni, 8% Cu, at a base temperature 1400°C, the following behaviour was observed for the Pt distribution ratio:Under the range of sulphur and oxygen pressure of this study (log pO2 from -15 to –12.2, log pS2 from – 4.6 to –2.2), the distribution ratio of Pt between matte and alloy was independent of the sulphur and oxygen pressure, having a value of 0.04.The Pt distribution ratio increased from 0.02 to 0.08 with temperature from 1340 to 1450 oC.For mattes where the proportions of Cu and Ni were kept constant, a slight decreasing trend was shown for the distribution ratio of Pt versus the iron content (37 to 53%) in the matte but was not confirmed because of experimental uncertainty."

Jan 1, 2003

By Vladimir E. Vigdergauz

"Bubble-mineral complexes could be formatted by an attaching of hydrophobic particles to the surface of air bubbles or by an evolution of bubbles from solution onto hydrophobic surfaces. Measurements of contact angles, detachment forces (DF), induction times (IT), evolution pressures (EP) and flotation recoveries (FR) for the studying of minerals wettability at various pH and electrochemical potentials were used. An analysis of the obtained IT results show that a process of bubble attachment to a mineral surface is a rather slow one and it will scarcely be enough for bubble-mineral complex formation under the conditions of real flotation.The ranges of adhesion potentials obtained by DF measurements, Figure 1, correlate with the data of floatability-potential for pyrite. The ranges of adhesion potentials obtained by DF measurements for galena (-1 ÷0.2V) and chalcocite (-0.5÷1.2V) correlate with the potential ranges of floatability for galena (<0.2V) and chalcocite (>-0.4V). An increase of the DF and the cathodic limit of the adhesion potential with increasing length of the hydrocarbon chain were observed. EP-pH curves for sulfides are a mirror-like to the DF-pH curves, Figure 2. Structure of solid-liquid and liquid-gas borders has a determinative importance for formation of bubble-mineral complexes and subsequently flotation results. Under vacuum on the mineral surface there are produced micro bubbles and preferably they will be appeared on the hydrophobic sites. Water structure breaks near a hydrophobic surface facilitate water mass destruction and formation of gaseous phase embryos under decompression in the impeller zone. It simultaneously reduces a probability of produced micro bubbles dissolution as a result of pressure increasing owing to constant fluctuation of liquid densities into impeller zone. Comparison of Taggart’s evaluation of the suction behind blades of the impeller of an agitation-froth machine and ABEP data on galena, Figure, shows that gas evolution will be observed in the range of 1300-2700 revolutions of impeller per minute for hydrophobic and hydrophilic surfaces successively."

Jan 1, 2003

By Ray Everson, Henry Kasaini

"Adsorption of Pd (II) anions on the surface of activated carbon (Norit 0.8) occurred at high proton concentration (0.01 – 2.5M, HCl) in the feed and averaged 27 mg/g. The adsorption process was interpreted in terms of surface ionisation and adsorption model. Enthalpy of adsorption averaged 0.4 kJ/mole indicative of an instantaneous physical adsorption process. We found that the Toth isotherm fit the adsorption data fairly accurately. A combination of the Langmuir and Freundlich equations yields an effective three-parameter Toth equation (1) which is frequently used to describe adsorption on heterogeneous surfaces.Figure 1 shows the comparison between experimental results and the model isotherms. We found that Langmuir isotherms underestimated the adsorption capacity on the porous surface while the Freundlich isotherm overestimated adsorption. Furthermore, the surface coverage at equilibrium was well described by both the Langmuir and Toth isotherms. But, Freundlich isotherm predicted a surface fraction coverage that was higher than unit. Based on better prediction of surface coverage and a reasonable fit to adsorption data, we concluded that the Toth isotherm best described the adsorption data of palladium. The adsorption process was limited by mass transfer resistance through the external film. We estimated the rate constant from equation (2), where e, ?b, and rp are porosity, fluid density and particle radius, respectively"

Jan 1, 2003

By R. X. Li

The overall flow-sheet of producing chromium (III) sulfate is described in this paper. The suitable conditions of each process such as sintering, leaching, aluminum removal, reduction, and de-composition conditions were experimentally studied. The results show it is reasonable to produce chromium (III) sulfate with the flow-sheet pointed out in this research work. The final product is Cr2(SO4)3 solution contained 150~250g/L Cr.

Jan 1, 2014

By Klaus M. Hahn, Hermann Wotruba, Bernd G. Friedrich

"Due to an increasing demand for nickel and cobalt and the depletion of nickel sulphide deposits worldwide, the production of ferronickel from lateritic nickel ores becomes more significant. About 60 percent of nickel reserves are present in laterite deposits. Common production methods like acid leaching or smelting operations implicate high material and energy consumption. Physical processing methods are also not efficient, because of the fine microstructural intergrowth of the minerals carrying valuable elements such as nickel and cobalt. Due to the high energy consumption of metallurgical treatment of lateritic nickel ore (nickel grade: 0.8 - 3.0%, Co: 0.05 - 0.15%), the separation of waste material (about 75 - 85%) before the metallurgical treatment is desirable. Therefore, an alternative process has been developed, combining a pyro-metallurgical pre-treatment with selected mechanical processing methods. The developed process consisted of a selective pre-reduction and non-selective segregation of the contained metal phases in the first stage. By this, the properties of the metal carrying minerals were changed and could become subject to concentration by means of fine beneficiation processes afterwards. The parameters of the pre-reduction and segregation were varied and the pre-treated samples were examined concerning their efficiency of metalization grade and metal grain size. This paper describes the investigation of pre-treatment methods of a lateritic nickel ore. The pre-treatment and possible subsequent separation methods were examined with regard to the recovery of the valuable elements. Metalization grade was around 80% for both Ni and Co with metal phase grain sizes below 20 µm. Scanning electron microscopy revealed distribution of new metal phases not only on the reducing agent, but also on the “slag” material.INTRODUCTION Nickel laterites are characterized as strongly weathered regoliths with several zones containing reserves of nickel (Ni) and cobalt (Co). These laterites are formed on serpentinites and ultramafic rocks under climatic and/or tectonic conditions that have changed over time (Butt & Cluzel, 2013). The formation of Ni laterites is influenced by numerous geological and environmental factors. In general, there are three ore types named according to the dominant Ni hosting minerals: oxides, hydrous magnesia (Mg) silicates and clay silicates (Butt & Cluzel, 2013). The most Ni laterite deposits contain two of these ore types, usually an oxide zone and an either clay or Mg silicate zone. Distribution of these principal deposit types, their average Ni-bearing phases and mean Ni grade are shown in Table 1. A schematic profile of the different deposits based on the development on serpentized ultramafic rocks is given in Figure 1 (Butt & Cluzel, 2013)."

Jan 1, 2018

By V. E. Vigdergauz

Possibilities of the analysis of potential energy of bubble-particle interaction on the basis of extended DLVO theory are discussed. Interaction energies of mineral silica, coal and pyrite particles with contact angles from 20 to 100 degrees and air bubbles in neutral and alkaline solutions are analyzed. It is shown that for hydrophilic silica, the formation of particle-bubble complexes (either in the area of primary or secondary potential minima) is impossible due to the high potential barriers (from 6000 to 140000 kT)and low values of the attraction force. There is shown that for coal and pyrite particles the energy of interaction vs. particle-bubble distance strongly depends on pH value. Improvement of floatability of minerals by the hydrophobization of their surface by collectors leads to the eliminating of potential barriers and the formation of the stable complexes of minerals and air bubbles in the area of primary potential minimum. In addition, due to hydrophobization of coal and pyrite changing pH has practically no influence on the energy of interaction. There are discussed results of the numerical calculations of normalized interaction forces in particle-bubble systems on the nanometer distances for pyrite, sphalerite, and chalcopyrite at contact angles up to 85° in comparison with the experimental data. The values of adhesion force for hydrophobized particles of coal and pyrite to air bubbles are about 10-5 N, that indicates stability of the formed flotation complexes. Examples of using the long-range and high-energy effect of hydrophobic interactions for improving minerals floatability are discussed. There are illustrated minerals wettability changes induced by the adsorption of thiol collector and hydrophobic polymer. Possibilities of flocculation and flotation of mineral slimes due the polymer-collector hydrophobic interactions are shown. Keywords: bubble-particle interaction, contact angle, extended DLVO theory, floatability

Sep 1, 2012

By R. L. Pascual, W. J. Whiten

"The froth flotation process is not well understood. Both flotation models, and the parameters used to describe the stream flows are not well defined. They in fact vary considerably in different applications. This creates difficulties is designing a simulation program suitable for use by plant personnel, consultants, and researchers. In addition to simulation, an effective simulation program can be expected to provide a range of other services.This paper shows how a process circuit simulator can be designed with sufficient flexibility to satisfy these needs, and discusses some of the additional services."

Jan 1, 2003