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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 K. Sasaki, H. Miki, Y. Muta, T. Hirajima, G. P. W. Suyantara

"Selective flotation of chalcopyrite and molybdenite is continuing problem since its selectivity is not perfect and current NaHS process needs closed system flotation plant because of hydrogen sulfide emission on acidic condition. Some alternative additives investigated as chalcopyrite became hydrophilic and molybdenite kept hydrophobic. XPS analysis indicated chalcopyrite became hydrophilic since iron and copper sulphate, hydroxide was covered on the surface whereas molybdenite kept hydrophobic since only molybdenite can be seen. Flotation experiments of chalcopyrite and molybdenite mixture sample indicated excellent separation that 95% of molybdenite can be recovered as froth and 93% of chalcopyrite can be recovered as sink. Flotation experiments with real bulk flotation concentration indicated similar separation result compared with current NaHS additive system. Possible mechanisms and detailed phenomenon were investigated based on the surface analysis and thermodynamic calculation etc. this alternative additive is easy to handle compared with NaHS since it does not emit effluent gas and commercially preferable.INTRODUCTIONMany copper mine often associates molybdenite (MoS2) as trace mineral. It is important to separate molybdenite and copper mineral efficiently since molybdenite is valuable mineral and also contamination of molybdenite into copper concentrate decrease concentrate value. Conventional separation of copper sulfide and molybdenite has been achieved with sulfide bulk flotation followed by selective molybdenite flotation with NaHS addition since NaHS works as a depressant for copper sulfide (Bulatovic, 2010; Ansari and Pawlik, 2007b). However, this current process shows imperfect molybdenite recovery (Liu et al., 2012, Zanin et al., 2009) and depressant such as NaHS needs to be used under specific flotation plant since it might be environmental contaminant (Ansari and Pawlik, 2007a). there are still unknown on the effect of depressant NaHS, but one of the theory is NaHS reductant effect. It is worth to investigate the effect of other reductant as depressant on chalcopyrite. On this research, typical reductant, Na2SO3 are added to utilize for selective flotation of chalcopyrite and molybdenite."

Jan 1, 2018

By Jun Qiu, Ping Chen, Xianjun Lu

Nitrogen of different forms from wastewater was adsorbed by the natural bentonite and modified bentonite. The effects of adsorption conditions on the nitrogen removal were investigated. The experiment results showed that natural bentonite could easily adsorb ammonia while poorly adsorb nitrate, the organic bentonite modified by octadecyl trimethyl ammonium could effectively adsorb nitrate with the removal ratio increased from no more than 5% to 89%. Two kinds of bentonite were added together to the simulated wastewater which contained ammonia nitrogen of 15mg/L and nitrate nitrogen of 10mg/L, the dosages were 1.0g respectively. Both ammonia and nitrate had significantly decreased on conditions that the oscillation time was 1.0h and room temperature 20?. The optimum pH value for ammonia removal was 7 while for nitrate removal was above 7. The adsorption isotherm fitting results indicated that the Freundlich adsorption isotherm was the better model to describe ammonia adsorbed on the natural bentonite and the saturated adsorption capacity was 10.25mg/L, while the Langmuir isotherm could better describe the adsorption of nitrate on the organic bentonite and the saturated adsorption capacity was 14.35mg/L. Fully considering the interaction between different ions and controlling the appropriate conditions, removing nitrogen from wastewater by adsorption of bentonite is an economic and effective method.

Jan 1, 2014

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 N. D. Dementieva

Based on lab and pilot-plant tests to recover gold, silver and lead of a Russian deposit, a collective and flotation concentration flow sheet with lead and sulfide concentrates was proposed. The type of the deposit is gold-sulfide-quartz-bearing. The recovery of gold, silver, and lead to a lead concentrate was 47.4%, 68.1% and 70.7%, respectively. The grade of gold and silver grade was 170 g/t and 372 g/t, respectively. The mass percent of lead, zinc and arsenic mass percent was 41.7%, 0.34% and 0.63%, respectively. The recovery of gold and silver recovery to a sulfide concentrate was 50.1% and 28.8% at the grade of gold 20.5 g/t and silver 66.2 g/t. Sulfide concentrate with arsenic mass percent ~3% was biooxidised followed by CIL and obtaining metal at the site as well as zinc concentrate from bioleaching solutions with zinc mass percent 45% at its 64% recovery. The total gold and silver recovery using a developed technology with the account of their treatment at a polymetallic plant was 92.2% and 93.7%, respectively.

Sep 1, 2012

By Matt Kilburn, Liming Lu, Steve Suthers, Alexander Edenton, Rodney Smyth, Matt Adam

"Magnetite concentrate is naturally good for pelletising. However, due to the depletion of reserves of traditional high grade hematite iron ore worldwide, the usage of magnetite concentrate in sintering is expected to increase substantially. Magnetite concentrate is typically high in Fe grade and releases extra heat when oxidised to hematite. This will not only improve the quality of agglomerates produced, but also have a potential beneficial impact on the fuel consumption of the agglomeration process. There are an increasing number of magnetite projects currently being considered and developed. However the concentrates from some of these projects are too coarse as pellet feeds and much finer and denser than normal sinter feeds. Accordingly, special strategies are required in order to utilise the coarse magnetite concentrates at high proportions in pelletising and sintering. This paper discusses various raw material preparation technologies and blending optimization methods demonstrated to be effective for improving the sintering and pelletising performance of coarse magnetite concentrates. Pre-granulation and addition of binders, such as hydrated lime, were found to be particularly efficient in recovering the sintering productivity of sinter blends containing magnetite concentrates. In pelletising, HPGR (High Pressure Grinding Rolls) grinding enabled production of good quality pellets from 100% magnetite concentrates and optimized blends containing up to 70% magnetite concentrates also formed good pellets.INTRODUCTION Magnetite concentrates are often used as feed materials for pellet plants or sinter plants depending on their grades and grain sizes. To achieve the required quality of green and fired pellets, the concentrates often need to be ground very fine (80% passing 38- 45 m), which inevitably consumes a great amount of energy. Therefore, efficient grinding processes are required to reduce the amount of energy consumption needed to achieve the sizing and chemical specification of pellet feeds. The use of magnetite concentrates in sintering has the potential to improve sinter chemistry, which is deteriorating over time due to the slowly decreasing grade of direct shipping iron ores around the world (Yang and Mathews, 1997; Yang and Witchard, 1998, Yang and Davis, 1999; Yang 2005). However, methods are required to allow the utilisation of high levels of concentrates in sintering while maintaining productivity and sinter quality (Han and Lu, 2017)."

Jan 1, 2018

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

Sep 1, 2012

By Mingxia Liu, Qi Liu, Tao Jiang

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

Jan 1, 2018

By N. Ahmed

This paper is concerned with the drainage behaviour of gangue mineral in the froth phase. Experiments were carried out in a continuous laboratory flotation cell in which froth depth and bubble size could be changed independently. The fraction of solids returning from the froth to the pulp zone was expressed using a rate constant. A mixture of hydrophilic solids (silica) and floatable particles (glass ballotini) was used as a flotation feed. Samples of glass ballotini of different hydrophobicities were obtained, using controlled silanation. Three samples, with contact angles of 50, 66, 82 degrees, were used. The effect of the initial bubble size (pulp bubble size), concentration of gangue mineral in the froth zone, and froth depth on the drainage of silica, were investigated. The drainage rate of the entrained solids increases with an increase in the degree of hydrophobicity of the floatable particles. Concerning the effect of pulp bubble size on the drainage rate of entrained solids, larger bubbles always give higher drainage rates due to formation of relatively loose froth structures which allow gangue particles to easily move down to the pulp zone. Conversely, smaller bubbles exhibit lower drainage rate constants, in particular at shallow froth depths.

Jan 1, 2003

By 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 Hamid-Reza Manouchehri, Hassna Aitahmed-Ali, Stellan Sundberg

"In flotation practices as the particle size becomes fine, e.g., p<20µm, the process efficiency declines markedly. When flotation of fine particles is necessary, one method to improve the recovery is selective agglomeration of fines. Different agglomerating methods have been introduced and tested; however, one method which has recently received great attention is to aggregate fine particles by magnetic force. A selective aggregation of the fine paramagnetic particles, e.g., sulfide minerals, can be achieved by applying a high intensity magnetic field during flotation conditioning. The method is simple, selective and effective for fines, and has a low operation cost. However, a minimum magnetic susceptibility of fine grains is required for this process. This method has been demonstrated in different sulfide minerals flotation plants. The implementation of the magnetic conditioning device, ProFlote, in both the Cu-Pb and the Zn circuit of Boliden’s Garpenberg plant in Sweden, where a complex massive sulfide ore is treated, is discussed herein. The preliminary results have shown an increase in the recovery of value minerals, in particular Zn and Ag and considerable reduction in Zn deportment to the final tail. Increases in Cu grade and decreases in Pb grade in Cu-con have been achieved as well."

Jan 1, 2014

By Tom Leistner, Urs A. Peuker, Martin Rudolph

"It is well known, that for conventional froth flotation techniques the processing of ultrafine mineral particles is generally inefficient and results in rather low-grade concentrates and relatively high losses of valuable minerals. Therefore, the investigation of other possible methods, which can selectively separate such fine particle systems effectively, is of considerable interest. In this study, the application of two-liquid flotation, a flotation-related process using oil droplets instead of air bubbles, is investigated as a possible processing strategy for the separation of ultrafine particle systems. The investigation involves the testing of the two-liquid flotation technique as simple laboratory-scale batch trials and moreover, the up-scaling to a semi-continuous process by using a modified lab scale flotation column. Magnetite and quartz particles, with particle sizes below 10 µm respectively, as academic mineral mixture and iso-octane and water as the two immiscible liquid phases are chosen for the experiments. To manipulate the wettability of the magnetite particles as well as the interfacial tension of the oil/water interfaces, surface active reagents of fatty acid basis are introduced in the system. The selectivity of the process is characterized by determining the removal of magnetite particles from the aqueous suspension through selective accumulation at the oil/water interface or extraction into the oil phase, respectively. Operational parameters including pH of the aqueous suspension, additional electrolyte addition and surfactant type as well as dosage are varied in order to maximize the efficiency and stability of the process."

Jan 1, 2014

By F. O. Milovich, V. A. Ignatkina, L. A. Samatova, E. D. Shepeta

"The aim of the research was to increase technological parameters of the flotation of finely disseminated scheelitecarbonate ore using selective reagent regime.In the studies the monomineral fractions of scheelite and calcite; samples of the scheelite-carbonate ore of the Primorsky deposit with the range of the carbonate module 3-65 were used. A carbonate module of ore is the ratio an initial assay of calcite to an initial assay of scheelite. Sodium oleate, iso-decyl alcohol, water glass, calcium chloride, soda or sodium hydroxide as flotation reagents were used. The flotation method in the Hallimond tube and in a mechanical cell, an adsorption method for study the kinetics of adsorption of oleate and isodecyl alcohol and its combinations on scheelite and calcite, IR spectroscopy including ATR to study the composition of surfacecompounds were applied. Selective reagent regime may include two ways - a combination of collectors or a modification of depressants of calcite and other gangue minerals. On one hand the combination of sodium oleate and higher fatty iso-alcohols of fractions C12-C16 in the rough scheelite flotation to reduce the flotation activity of calcite has been studied. On the other hand depression of calcite flotation by calcium chloride with water glass into rough flotation was used; modified the steaming cycle by Petrov's method applying change the concentration of water glass and other. Fatty iso-alcohols can adsorb on the surface of the calcite that reducing the adsorption of sodium oleate and floatability of calcite has been fallen. Their co-adsorbing with oleat on the scheelite surface were support the hydrophobization and flocculation of slime particles of scheelite. Flocculation of the particles of scheelite leads to increased up 3 times of the recovery of scheelite from the slime class, and calcite change up only 1.4-1.1 times it’s recovery.The growth of the carbonate module more than 11 is decreased the assay of WO3 in the scheelite concentrate of selection cycle."

Jan 1, 2018

By K. Saberyan

Zirconium and hafnium are two important elements in nuclear industries. Zirconium is used in fuel rod for its low neutron absorption. Hafnium should be separated from zirconium, because it has higher neutron absorption cross section. In this research, separation process of the mentioned elements from (Zr+Hf)Cl4 mixture produced in the Zirconium production plant (ZPP) of Iran (Esfahan) was studied employing solvent extraction method in the nitric acid medium by using tributylphosphate (TBP) as solvent, and kerosene as diluent. The effects of nitric acid, sodium nitrate and amount of extractant, zirconium concentration in aqueous phase, phase ratio, agitation time, and mixer agitation rate were investigated on the separation process. The process was optimized at 5 M nitric acid, 1 M sodium nitrate, 60% (v/v) TBP. The optimum values for phase ratio, agitation time and agitation rate were 1.5 min and 500 rpm respectively. In this condition, the zirconium extraction efficiency, and separation factor were 65.1% and 205.59, respectively. Finally, we accessed to nuclear grade in this research.

Jan 1, 2014

By S. V. Petrov

Oxidised ores possess a significant share among raw materials which are treated by traditional plant technology. As usual, the chemical composition of these ores is rather simple. They can be treated by standard cyanidation. In this case, the resulting wastes have an alkaline reaction. Their toxicity (in case of ROM ores treatment) is mainly due to the presence cyanides and thicyanades. The tails are dexotified before disposal. However, chemical reagents used cannot provide a complete removal of toxic matters. In this case, this disposal poses a real problem because these tails contain a significant amount of CN and SCN and their behavior during a long disposal should be studied. A sample with a simple composition taken from cyanidation tails was studied. The sample presents itself the quartz low-grade sulfide gold-bearing ore. Sulfide sulfur content is 0.15 per cent,and heavy metals content is 0.023 per cent. Method of testing is described further. The samples were tested under moderate and subarctic climates based on the difference in temperature, moisture and the degree of oxygen saturation of air. The pH of water extract, which was prepared using distilled water, was also determined besides measuring the concentration of cyanides and thiocyanates. This demonstrates the stability of sulfide-bearing minerals in the disposed tails. The tests time was 820 days. It was found that the alkalinity of the samples tends to lower under oxygen-containing conditions in proportion to temperature increasing. Under conditions without oxygen, the pH lowering is minimal. Mineralogical and chemical properties of the ore material give positive alkaline balance during testing. The solid sample contains enough alkaline agents to compensate dangerous to the environment reactions of sulfides oxidation.pH value maintaining under alkaline conditions witnesses to the possibility of a safe disposal of this tails type. The largest amount of cyanide is removed under acid-containing conditions at positive temperatures. The higher the temperature is, the more intensive destruction is. At the moment, of finishing the tests at 20ºC temperature, the residual concentration of CN- was 0.06-0.10 mg/L, at 4ºC, the residual concentration of CN- was 0.2-0.3 mg/L and at -18ºC was 0.4-0.6 mg/L. Under conditions with the lack of oxygen, cyanides can be removed within the first 200 days. Then, this process fully stops. A stabilized cyanides concentration is 3.0-4.0 mg/L. The presence of sulfides increases the content of cyanides at the initial stage of testing. Then, the concentration of SCN at the temperatures above 0ºC decreases rapidly under oxygen-containing conditions. At the rise of temperature, a narrowing of peak at the curve and an increase of the destruction process are observed. At the end of testing, the concentration of thiocyanates in the moisture of wastes was 0.2-0.3 mg/L at the temperature of 20ºC and 0.5-0.6 mg/L at the temperature of 4ºC, respectively. The concentration of thiocyanates contained in a frozen sample and media which have the lack of oxygen stabilizes at a certain level owing to sulfides and does not practically change further. It was found that detoxification of oxidized cyanidation tailings with a simple composition which were disposed as filtration cakes can be possible. In this case, the concentration of cyanide in the moisture of disposed wastes can have a close value or equal to actual concentration during cyanidation. In order to meet the requirements of high ecological safety standards and successful detoxification process of toxic compounds in the tails under the action of natural factors, the conditions of air aeration with oxygen for the whole volume of tails are required. Keywords: cyanides, thiocyanates, storage, detoxification, flotation cakes

Sep 1, 2012

By Yuri L. Nikolaev

The treatment of placer gold with fine gold, associated with gold-bearing sulfide minerals, heavy minerals and oxidized minerals such as manganowolframite (gubnerite) is not an easy task. In this case, this complex material cannot be treated using physical separation methods such as deep concentration and finishing, magnetic separation and solvent extraction. This technology is usually employed in gold washings finishing plant. The easiest way to recover precious metals in the form of an easy-to-sample saleable product is metallurgical treatment. This paper describes the application of pyrometallurgical processes with oxidative roasting, re-cleaning of cinders (if required) and ore-thermal smelting for producing gold bullion. Hydrometallurgical treatment of slags as an additional operation is recommended in order to maximize recovery of valuable metals. After this treatment, a barren leaching cake rich in PGM can be sold in the market. PGM can be collected as gold-silver alloy during smelting which allows the phase formation of polymetallic matte due to specific composition of fluxes. The PGM are then in the form of saleable gold bullions in the refinery.

Sep 1, 2012

By Kirsten Corin, Margreth Tadie, Michael Nicol, Cyril O’Connor, Jenny Wiese

"The recovery of base metal sulfides has been emphasized in the study of the flotation of platinum group minerals (PGMs). However, in some ore bodies such as the Platreef of the Bushveld Complex, sulfide minerals do not make up the majority of the more significant PGM mineralization. It is therefore important to develop a fundamental understanding of how non-sulfide and sulfide PGMs respond respectively to the current reagents being used in the flotation of these minerals. The interactions between platinum and palladium sulfides and tellurides with the thiol collectors, ethyl xanthate and diethyl dithiophosphate, have been studied using the electrochemical techniques of mineral rest potential and voltammetry measurements. The differences in the interaction between the two types of minerals with these reagents were of key interest. Rest potential measurements indicated stronger electrochemical interactions of the minerals with ethyl xanthate than diethyl dithiophosphate. These measurements also indicated that there are different forms of oxidized collector present on the mineral surfaces after interaction with ethyl xanthates. Voltammetry measurements support these observations and suggest differences of adsorption on Pt and Pd sulfides than on Pt and Pd tellurides. Voltammetry also showed that there was minimal electrochemical interaction between the Pt and Pd minerals and diethyl dithiophosphate."

Jan 1, 2014

By Yi-jun Cao, Jin-cai Ran, Guo-sheng Li, Jiong-tian Liu, Li-jun Deng, Shu-lei Li

A fly ash sample from a power station in Guangdong province has been characterized by size separation, X-ray diffraction, contact angle measurements and X-ray Fluorescence. The ash sample had a loss-on-ignition (LOI) (%) of 15.54% and a large proportion of the unburned carbon was distributed in the +74 µm and -20 µm fractions. Contact angle measurements suggested that the removal of unburned carbon from the fly ash using flotation would present some challenges. The effects of various operating variables on the removal rate of unburned carbon (RUC) (%) and (LOI) (%) were determined using a cyclonic-static micro bubble flotation column (FCSMC). Within the range studied, the optimum diesel oil dosage was 1200 g/t, abies oil (frother) dosage was 600 g/t, pulp density was 20%, superficial gas velocity was 1.4 cm/s and circulating pressure was 0.20Mpa. Column flotation tests indicated that the FCSMC method a viable and effective separation process for removing the unburned carbon from the fly ash. Under the optimized conditions, a clean ash with 2.13% LOI and 94.21% RUC was obtained.

Jan 1, 2014

By Henrique Kahn, Daniel Uliana, Juliana Antoniassi, Viviane Shimizu

"Mineral exploration and geometallurgy require a large number of samples for physical, chemical and mineralogical assays. The combination of all these data and their spatial distribution define the ore variability. This is important in exploration programs and crucial in feasibility studies as well as at the production operation level. Ore mineralogical composition and its associations, characterizing the geological formation and mineralization, are the main keys to define the ore domains and its variability, which can be quickly assessed by cluster analysis and by modern automated mineralogy tools. One hundred and ten copper ore samples from Sossego mine, in Brazil were compared and classified by X-ray diffraction cluster analysis based on the position and the intensity of the diffracted peaks. Initially four ore types were categorized based on content of major minerals: quartz, feldspar, amphibole, iron oxides, mica and chlorite. Results showed a strong correlation between the grouping and the samples location in Sequeirinho and Sossego orebodies, with a straight link to types/intensities of hydrothermal alteration prevailing in each body, which reflects the mineralogical composition and thus the X-ray patterns. Samples from four recognized ore types were submitted to detailed automated mineralogical studies by electron beam image analysis and differ strongly from each other regarding their chemical and mineralogical compositions and relevant parameters for mineral processing. Chalcopyrite is essentially the only valuable mineral, occurring both as submillimetric grains included in other minerals and as larger crystals. Except for pyrite, other sulfide minerals occur as traces. Chalcopyrite liberation curves indicate that samples from Sossego have higher liberation degree than those from Sequeirinho. The proposed method proved to be very efficient and accurate to classify a large number of samples within a short time frame, allowing the distinction of the ore types regarding their mineralogical composition as well as the mineral processing parameters."

Jan 1, 2014

By David I. Verrelli, Peter T. L. Koh

"Recent experimental measurements of induction time made by direct observation with the ‘Milli-Timer’ indicated that angular particles were able to attach much more rapidly than spherical particles. There was around a tenfold difference in the respective induction periods for particle-bubble attachment. For industrial application, a more holistic comparison is needed, with the induction period for attachment being just one input. Over the years, CSIRO has developed a CFD-flotation model that incorporates both rigorous hydrodynamics, to simulate real industrial cell geometries, and a detailed model of the embedded flotation process, in which the induction period is an important parameter. We conducted transient modelling of batch flotation. First, spherical particles were modelled, as a ‘baseline’, for different particle sizes and levels of hydrophobicity. In the second set of results, the induction period was decreased by a factor of up to ten, simulating flotation of angular particles. Flotation recovery was found to depend upon induction period in a complex manner. For highly hydrophobic or fine particles, the induction period for spheres was already so low that recovery was limited by other factors (e.g. bubble-particle collision frequency). Further decreases in induction period, as for angular particles, did not have a significant effect on recovery in these cases. By contrast, when weakly hydrophobic or coarse particles were modelled, the recovery was predicted to be greatly enhanced for angular particles, in comparison to spheres. For these particles the induction period was limiting recovery, so that the flotation rate constant could be improved directly by reducing the induction period. This is consistent with batch flotation experiments using Ballotini reported earlier. Therefore, when dealing with weakly hydrophobic particles or relatively large particles that are to be floated, an enhancement can be expected for more angular particle shapes. In such cases, judicious specification of the grinding circuit may improve the overall efficiency."

Jan 1, 2014