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By B. P. von der Heyden, P. Neethling, M. Tadieb, L. Babedi

The effects of trace element substitutions in sphalerite mineral structure on optimised floatation response have, as yet, not been fully constrained or fully understood. To further this important field of study, this contribution focusses specifically on mineral and surface chemistry, and electro-chemistry of Cd- and Co- substituted synthetic sphalerites using Raman spectroscopy and Zeta potential experimentation. Raman spectroscopy illustrates that the presence of these impurities results in the introduction of a new mode, the relative intensity of which can be correlated (Cd r2=0.95 and Co r2= 0.99) to the dopant concentration. Comparison to X-ray Diffraction results measuring the unit cell parameter further shows that this relative intensity (Cd r2=0.81 and Co r2= 0.99) may provide insights into the degree of lattice strain within the mineral structure. The zeta potential distribution of an un-activated Cd-sphalerite show no detrimental effect as function of Cd content. Although the iso-electric point shifted from 2.45 at 1 wt.% Cd to 2.69 at 3.68 wt.% Cd, the zeta potential remained negative at alkaline media. Conversely, cobalt at low concentration of 0.36 wt.% had a detrimental effect on the surface charge, resulting to a close to neutral zeta potential at different pH. The adsorption of Cu ions on the surface of Co-bearing sphalerite conditioned in an alkaline media slightly increases the zeta potential of Co-sphalerite. While the Cd-bearing sphalerite decrease in negative zeta potential at >1 wt.% Cd indicating a complete exchange between Cu and Zn. The results presented herein illustrate that, based on the chemical nature of the substituting metal; sphalerite will exhibit multiple response to flotation reagents. Maximum recovery of zinc can thus only be achieved through multidisciplinary study and fundamental understanding of the effects of cation substitution on mineral structure and surface chemistry, the latter necessarily affecting the floatation response.

Jan 1, 2018

By W. Kobal

The extraction of nickel (Ni) and cobalt (Co) from the laterite deposit of Ramu nickel-cobalt Project in Papua New Guinea was performed in this study. Chemical analysis by Inductively Coupled Plasma (ICP-AES) atomic emission spectrometer, SPS-3000 (Seiko Instruments (Inc.), shows the ore contains 48% Fe, 1% Ni, 0.1% Co, 1.8% Al, 0.14% Mg, and 0.8% Mn. Characterization by X-ray diffraction (XRD) analysis of the laterite ore obtained from the mine site shows the ore contains 70 to 80% goethite (FeOOH), assuming Fe content of 48% is mainly from geothite. The main leaching parameters investigated include; slurry temperature, leaching time and sulphuric acid (H2SO4) concentration to evaluate nickel and cobalt extraction. For all experiments, 10g batch samples are put into 300 ml beaker containing 100 ml of sulphuric acid of varying concentrations (1M, 2M, 4M). During the leaching period, 5 ml slurry samples are withdrawn at different times and filtered to obtain filtrate for ICP analysis to monitor nickel and cobalt extraction. Solid samples at the end of all tests are also obtained by filtration and after drying, XRD and ICP tests are performed to monitor nickel and cobalt contents. According to the test results performed at normal atmospheric pressure, over 99% of nickel and over 50% cobalt were extracted into solution within 120 min at 95ºC in 2M H2SO4 solution. Similar results were obtained when only temperature was reduced to 90ºC, but cobalt extraction increased to over 70% when leaching time was increased to 240 min. Further reduction in temperature to 80 and 60ºC resulted in reduction of nickel and cobalt extraction. At the end of each leaching test, magnetite was seen to attach to magnetic stirrer. The study showed nickel can be completely leached into solution but cobalt only up to 70%. Keywords: atmospheric pressure, sulphuric acid leaching, nickel laterite

Sep 1, 2012

By L. Stamenov, H. Bouzahzah, S. Gaydardzhiev, D. Naumov

"The Chelopech epithermal arsenic bearing high-sulphidation, copper-gold deposit located in Bulgaria is often referred as the richest European gold deposit currently under exploitation. Key points from the flotation circuit of the processing plant have been sampled and selected physicochemical parameters measured. Plant survey has followed with selected samples being submitted to chemical and mineral liberation analysis (MLA). Quantitative analysis has enabled to link the flotation response of the main copper bearing minerals with the physiochemical parameters (Eh, DO, EDTA extractable Cu and Fe) being measured. Data from mineral liberation analysis have highlighted an important process-relevant information explaining the variable floatability in the various granulometric classes.The low chalcopyrite recovery could be linked to the non-sufficient amount of dissolved oxygen measured in the copper selective flotation circuit. Given the finely-disseminated copper bearing minerals, the observed copper losses inside the flotation could be also explained by the insufficient degree of liberation of the mineral grains. Suggestions for improvement in metallurgical recovery are therefore proposed.INTRODUCTIONThe Chelopech deposit is a high sulphidation (HS) volcanic-hosted epithermal gold-copper one (Bonev et al., 2002; Kouzmanov et al, 2009; Strashimirov, et al. 2002). It is considered as one of the largest and economically most important ore deposits in Bulgaria, and often is referred to Europe’s largest currently mined gold resource. It is located in the Srednogorie zone which falls within the central sector of the extensive Tethyan–Eurasian copper belt formed during Mesozoic–Cenozoic time along the southern margin of Eurasia. The Srednogorie zone has the features of a subduction-related, Late Cretaceous island arc, with development of a calk-alkaline to sub-alkaline volcano-plutonic magmatism and associated hydrothermal ore deposits (Bonev et al., 2002).Ore mineralisation occurs as veins, mineralised breccia, and massive sulphide replacements and disseminations. Three mineralisation stages have been identified at Chelopech deposit. An early pyrite–marcasite mineralisation (stage I), characterised by disseminated to massive pyrite followed and partly brecciated by enargite– luzonite and tennantite–chalcopyrite–bornite (stage II) mineralisation. The gold is met in ores belonging to the stage II. Sphalerite and galena veins characterise stage III, best developed below and adjacent to the pyrite–enargite– chalcopyrite ore bodies. Advanced argillic altered volcanoclastic rocks commonly host this mineralisation (Chambefort and R. Moritz, 2014)."

Jan 1, 2018

By J. Wiese, K. Corin, Z. Song

"Relating flotation performance to the electrochemical characteristics of a pulp is complex both in fundamental research and in practice. In the case of thiol collectors, different Eh values in the flotation system can result in the formation of the dimer or the metal thiolate which may or may not enhance the hydrophobicity of the mineral. Reducing or oxidizing conditions in a flotation system, viz. changing the Eh value, are usually manipulated to achieve an optimum flotation response by control of pH and dissolved oxygen levels in the system. A variation in pulp potential may also be achieved by the addition of potential modifiers such as sodium hydrosulphide (NaHS), sodium hypochlorite (NaClO) or hydrogen peroxide (H2O2). There exists anecdotal evidence which suggests that the addition of small amounts of H2O2 to the flotation process can improve sulphide mineral recovery. The objective of the present study was to investigate the effect of the addition of the potential modifier, H2O2, on sulphide mineral recoveries and grades in the flotation of sulphide minerals from two copper bearing ores from China and compare the results to those obtained for a PGM bearing ore South Africa. Batch flotation tests were conducted using the three different ores at the natural pH of the different systems, in the presence of a xanthate collector and the absence and presence of H2O2 as a potential modifier. The results indicate that the addition of carefully controlled low concentrations of H2O2 resulted in improvements in flotation performance. INTRODUCTIONElectrochemical potential as a control parameter in the flotation of sulphide minerals has been widely studied (Allison et al., 1972; Gardner and Woods, 1979; Ross and Van Deventer, 1985; Chander, 2003; Woods, 2003; Javadi, 2013). There is concensus that in order to be recovered during flotation, sulphide minerals require a suitable redox environment. During the flotation process thiol collectors and sulphide minerals are involved in electrochemical reactions which result in the formation of hydrophobic species at the mineral surface (Finkelstein and Goold, 1972; Rand and Woods, 1984). Sulphide minerals act as semiconductors and electrons are transferred during the interaction of the mineral with collector. The resultant potential difference and its magnitude are responsible for the transfer of electrons and the rate of the reaction (Bard and Faulkner, 2001; Fuerstenau et al., 2007). Reducing or oxidizing conditions in a flotation system, viz. changing the Eh value, may be manipulated to achieve an optimum flotation response by control of pH and dissolved oxygen levels in the system (Heyes and Trahar, 1979). The use of potential modifiers viz. reducing or oxidizing agents which include H2O2, NaClO, and NaHS, is an alternative method by which to control the potential of the pulp in a flotation system which may or may not promote the flotation of desired minerals (Rao, 2004). The oxidizing agent, H2O2, undergoes a cathodic reaction which can result in the enhanced flotation of valuable minerals. The potential of the system is increased which results in a shift in the mixed potential of a mineral. The magnitude of the over-potential influences the rate of the oxidation process and thus the flotation response of sulphide minerals (Kocabag and Guler, 2008). Equation 1 shows the proposed oxidation of xanthate by H2O2 (Lipkina and Streltysn, 1970)."

Jan 1, 2018

By Evgeni Visariev

In Copper smelter Aurubis Bulgaria, the copper in slag from the Flash furnace and the Converters is recovered by flotation. The scheme of slag processing is crushing, two stage grinding (autogenous and ball) and flotation. Till 2010 the grinding cycle in the plant was in two stages ? the first stage was AG Mill 70?23 working with a classifier and the second stage was ball mill 3.6/5.5 working with a hydrocyclone. In 2010 a new AG Mill 65x78 with hydrocyclone was put in operation in order to increase throughput of the plant. The second stage of the grinding cycle is with the same ball mill. The Old AG mill processed 55-60 t/h slag with particle size -0.071 mm 75% or over 75 t/h with particle size -0.071 mm 35-40 %. The new AG Mill was designed for throughput 105 t/h with particle size -0.071 mm over 70 %. After the start up there were some problems with the equipment ? block up of AG Mill?s grate and pumps for feeding of the hydrocyclone. For optimization of the process a lot of general tests were made. One of the main problem was a wearing of the sand nozzles. Different materials (rubber, ceramic, metallic) for the sand nozzles were tested. The openings of the grate were changed. This paper presents: ? the optimal technological parameters of the old and the new working scheme; ? how the technological parameters of the new working scheme change when the hydrocyclone works with different nozzles; ? the effect of the change of the grate openings; ? the problems with the increase of the circulating load; ? a final decisions for improvement of the grinding cycle work. Keywords: spigot, wearing, classification, effectiveness, circulating load, autogenous, mill

Sep 1, 2012

By M. V. Sowmya

Batch biosorption experiments were carried out for the bio-remediation of Cr (VI) ions from aqueous solutions using Serratia marcescens, a Gram negative, heterotroph and Gram positive bacterial isolates from a chromite mine. The influence of various experimental parameters such as contact time, pH, concentration of Cr (VI) ions and amount of biomass was evaluated with respect to the uptake of Cr (VI). The bio-sorption of Cr (VI) was found to be quite rapid and the percentage biosortion was found to increase with increase in the equilibrium chromium concentration. The free energy of biosorption of Cr (VI) was estimated to be in the range of -23 to -25 kJ/mol for the chosen bacteria. The uptake of chromium by the bacteria was confirmed by EDX and FTIR spectroscopy. As a follow up of this study, bacterial strains resistant to hexavalent chromium were isolated from a chromite mine in Karnataka, India and identified as Arthrobacter sp., Micrococcus sp. and Exiguobacterium sp. using 16s rRNA sequencing. The efficacy of the bacterial isolates for Cr (VI) uptake was assessed and over 90% bioremoval could be achieved for Serratia marcescens and Micrococcus sp. isolate. Possible mechanisms of chromium uptake by the microorganism are discussed. Keywords: bioremediation, hexavalent chromium, biosorption, bioreduction

Sep 1, 2012

By T. N. Matveeva, T. A. Ivanova

"The article presents the results of the research aimed at development and testing of new effective reagents – collectors and green modifiers for more complete extraction of gold and platinum to concentrates at reduced loss with waste products. The main deposits of Au and PGM ores of Russia and abroad are presented by refractory raw material with the non-uniform finely-interspersed sulfide mineralization, submicron gold and platinum, the low metal content, non-uniform distribution of valuable minerals. and show low indicators of recovery. The main losses of precious metals (up to 15 %) at flotation are associated with thin slam tailings because of inefficiency of standard reagent modes.In the paper, the new trends in design of collecting agents for extraction of gold and PGM sulfide minerals and their application in flotation tests are substantiated. The original technique for obtaining the modified collector reagents – dithiocarbamate, dithiophoshpinate and dithiazine, incorporated non-ionic compounds that are able to generate stable complexes with gold and platinum has been developed. A novel class of collectors – cloud point polymers showed high flotation recovery of fine particles of gold and platinum. The original technique to create the mineral samples of natural sulfides with ""invisible"" or sub-micron gold on their surface designed helped to indicate the mechanism of selective adsorption of novel agents on Au and Pt-sulfide minerals. Extractive UV spectrophotometry, potential measurements, X-ray phase and spectral analysis, scanning electronic microscopy (SEAM), laser SIM and AFM microscopy were applied to analyze the adsorbed layer of modified reagents on the mineral surface. Selective hydrophobic covering on the surface of micro- and nanoparticles of noble metals provided an increase in their extraction during flotation. New reagent modes of modified collectors and green modifiers were tested in scaled-up laboratory flotation and the results obtained demonstrated the increased quality of the concentrates in terms of gold content by 1.5 times and higher gold recovery by 1.5-5%. The studies have been supported by Grants of the President of RF “Scientific School of Academician Chanturiya” NSh-220.2012.5; NSh-748.2014.5."

Jan 1, 2018

By S. Castro

Molybdenite flotation is strongly depressed at pH higher than 9.5 in the flotation of Cu-Mo ores in sea water. Chemically sea water contains mainly Na+ and Cl- ions, but also some secondary ions, such as SO42-, Mg2+; Ca2+, HCO3-; etc., which are not necessarily indifferent for the flotation of molybdenite. The natural floatability of molybdenite in sea water and in NaCl solutions containing different secondary ions is investigated by micro-flotation tests. The tests indicate that the floatability of molybdenite in alkaline media in 0.6 M NaCl solutions is not affected by the presence of anions, such as, SO42- and HCO3-, at concentrations similar to those occurring in sea water. However, a strong depression of molybdenite at pH ranging from 9.5-10.0, is produced by the alkaline earth metal cations (Ca2+ and Mg2+ ions), dissolved in distilled water or in 0.6M NaCl solutions. It was found that effect of Mg2+ions is significantly stronger than Ca2+ ions. Effect of both ions is attributed to hydrolysis and adsorption of MOH+ hydroxy-complexes. This is followed by subsequent precipitation of hydrophilic colloidal hydroxides at the molybdenite/solution interface, and in bulk solution.

Sep 1, 2012

By Y. H. Hu, X. X. Zhang, Z. F. Dai, H. J. Huang, Q. S. Huang

"In order to get a more comprehensive understanding of the interaction of fine fluorite particles and bubbles, the electro-flotation was conducted, a high speed CCD was used to determine the bubble size distribution, and the results were analyzed using the models of collision and attachment. The electro-flotation was performed in a modified Hallimond tube. The results show that for different fluorite with size of 0 -10µm, 10 -38µm, 38-74um, there is a matching range between the different particle sizes and cathode aperture size (38um, 38um, 74um) to reach highest recovery. In addition, improving the concentration of collector is benefit for the flotation recovery due to the ability of collector to decrease the bubble size and prevent the merger of bubbles. Furthermore, theoretical calculation of collision, adhesion probability and collection probability is in agreement with the experimental data for electro-flotation recovery of fluorite.INTRODUCTIONFluorite is widely distributed, and has been found in more than 40 countries around the world. As fluorite minerals are easy to float, flotation is used as the best method of the current recovery of fluorite (Yang and Ai, 2016; Chen et al., 2017). In the field of mineral processing, the flotation of fine particles is particularly difficult, caused by the small quality and large surface (Sun et al., 2006). Flotation is now considered to contain three subprocesses, including the collision, attachment and detachment between the particles and bubbles (Sun et al., 2011). The collision of particles with bubbles is related to factors such as particle size and density, bubble size, bubble rise rate (Qin et al., 2012). Zongfu Dai et al. (2000) summarized the particle-bubble collisions models in detail and compared the experiment results with the model predictions. However, particle-bubble interactions occur in complex and turbulent flotation environments (Xing et al., 2017). Both thermodynamics and dynamic factors affect the adhesion of particles on bubbles surface (Schulze, 1989; Shahbazi et al., 2010). Scheludko et al. (1976) believes that the necessary condition for successful adhesion of particles on bubbles is that the contact time is greater than the induction time. The probability of adhesion between particles and bubbles increases with the increase of bubble size, but if the particle size is too small, the probability of adhesion decreases instead (Ren, et al. 2014; Norori- McCormac et al., 2017). After the particles adhere to the bubble surface, the particles will slide down to the bottom of the bubble due to gravity. At this point, the gravity, inertial centrifugal force and fluid force promote the desorption of particles from the bubble surface, while the surface tension, surface hydrophobic force maintain the stability of particles-bubble combination (Ralston et al.,2017). In addition, in the process of rising to the foam layer, desorption can also occurs. The purpose of this study is to observe the flotation behavior of fine fluorite with different size and to get a more comprehensive understanding of the interaction of fine fluorite particles and bubbles."

Jan 1, 2018

By A. J. Lynch, D. K. Tungpalan, Y. Reja, E. C. Avelar, G. Figueroa, S. Gómez, R. Alanis, M. A. Corona-Arroyo

"Have you been on a mine site? This question was posed by Emeritus Professor Alban Lynch to Higher Degree by Research (HDR) Students from the Sustainable Minerals Institute - Julius Kruttschnitt Mineral Research Centre (SMI-JKMRC) in the Student Technical Presentations in 2015. From that question, five HDR students from SMI-JKMRC organised a placement on mine sites in Mexico. The SMI-JKMRC is well known for its tradition to provide their students with opportunities to enhance and test their skills in mineral processing plants. The Student Venture became a short internship for HDR students which had the objective of establishing collaboration with mining companies in Australia and overseas, and of providing a unique experience for the HDR students in regard to their training, professional development, networking and cultural interchange. In return for the companies’ support, the students conducted plant audits to evaluate the process performance thereby providing valuable data to the host company. The 2016 Student Venture was held at the Grupo Peñoles & Grupo Fresnillo in Mexico, in which three mine sites received five HDR students from JKMRC and one young researcher from Universidad de Guanajuato (UG). This paper describes the positive outcomes for the mining company and the students for this experience. The Venture was considered very successful, as it provided valuable training for the students as well as in depth information about the operation of the comminution and flotation circuits of the host sites for the Grupo Peñoles & Grupo Fresnillo. The experience also provided an opportunity for an exchange of knowledge between the HDR students and the site personnel from the host operations. The indication of the success of the experience for all involved was the support of the host company in future student internships."

Jan 1, 2018

By Yagmur Sirinyurt, Ayhan Ali Sirkeci, Gülay Bulut, Mustafa Özer, Tuncer Acar

"The basic requirement of glass industry for the silica sand is at least 99% SiO2 content. On the other hand, coloring impurities such as Fe and Ti, must be removed. Flotation is the most widely used method for the purification of silica sands from impurities. In this study experimental studies were carried out to reduce Fe content of Mersin (Turkey) district silica sands by flotation. Silica sand sample with a d80 particle size of 1.85 mm was reduced below 0.5 mm in size. Then the size fraction -0.5 +0.106 mm was subjected to flotation tests. In flotation tests, sulfonate-type R801-R825, fatty acid based DER NA 7 (Produced by a Turkish company) and HA110-HA150 a blend of various chemicals produced by Mersin Cam-Is Mining Company (producer of glass raw materials) were used as collectors. Flotation tests showed that sulfonate type R801-R825 collectors provided much better results in acidic medium (pH: 3). The optimum pH value for DER NA, HA150 and HA110 collectors was found to be 7. It was observed that the addition of collector at once caused an increase in the amount of floated product that resulted in a loss of silica to the tailings. In the case of multistage addition of the collector much better selectivity was achieved. As a result of flotation tests conducted under best conditions, a concentrate assaying 0.046% Fe was obtained with a weight percentage of 93.4 when DER NA 7 was used as a collector. In the case of R801-R825 a concentrate was produced with 0.058% Fe content with a yield of 98.4%. On the use of HA150-HA110 the concentrate was produced with 96% weight recovery and 0.052% Fe content."

Jan 1, 2014

By D. I. Verrelli

Within the flotation community a belief has developed that some particle shapes are more ?floatable? than others. This is usually attributed to an influence of particle shape or roughness on the induction period required to achieve attachment between the particles and the air bubbles in the pulp. Up to now, such measurements have not been able to readily isolate the effect on individual flotation subprocesses. In contrast, our experimental apparatus, the CSIRO Milli-Timer, enables us to directly observe the process of particle?bubble interaction and attachment by means of a high-speed video recording, thus providing a direct measure of the induction period for attachment. To assess the influence of particle shape on induction time we used two varieties of methylated borosilicate glass particles ? spheres and angular ?frit? ? in a range of tightly-sized fractions. In doing this, we take care to account for the influence of other factors that could affect the induction time, such as the polar angle of sliding commencement, and approach velocity. These parameters are recorded as variables for each interaction, and corrected for using multiple nonlinear regression. Our results illustrate the importance of particle shape on induction period, with angular particles exhibiting induction periods that were an order of magnitude lower than those of spheres. Furthermore, the induction period was seen to decrease with increasing particle velocity, or kinetic energy on approach, but increased as the trajectory approached the limit of just grazing the bubble. Particle shape in mineral processing is a consequence chiefly of the mineral type and the type of grinding employed. The results presented herein indicate that attention should be paid to the shape of particles obtained from the grinding operation, besides particle size. Keywords: attachment, bubbles, flotation, induction period, particles, shape effects, surface roughness

Sep 1, 2012

By Y. C. Liu

Arsenic bearing copper-gold ores deposit have been found in most areas of China, especially in southwest. Due to the very closed association between arsenic, copper and gold, conventional flotation and cyanide leaching process may not give positive results. An arsenic bearing copper-gold ore in Sichuan province ,with gold grade of 10.12 g/t, 0.6% Cu and 0.14% As, is characterized by superfine grains with -40 microns fraction accounting for 70.9% and the gold enwrapped mainly by pyrite and tennanite accounts for 34.31%. Arsenic in this ore occurs in isomorphism, deposited in tetrahedrite. The ore was processed primarily in two stage flotation to get copper bearing gold concentrate and pyrite bearing gold concentrate respectively, and sequentially processed by leaching. Under the pressure of 300 KPa and 110~115 ?, the copper-gold concentrate was leached by an oxidizing and catalyzing leach agent then copper and gold were separated from each other in leach solution. The pyrite bearing gold concentrate was processed by cyanide leaching with the leach residue as sulfur product. The test results showed that copper recovery was up to 88.89%, gold recovery up to 89.18% and sulfur recovery up to 92.64%.

Jan 1, 2014

By M. Prasad

Growing concern over increased levels of atmospheric carbon dioxide has prompted new interests in development of materials and techniques for its sequestration. Various research and developmental work on different aspects of carbon capture technology are being extensively carried out worldwide. The main objective of the present work is to synthesize a HAS material having high capacity and robust ability for recycling to capture greenhouse gases with special reference to carbon dioxide (CO2) from the sources from where it is released to the atmosphere. Existing CO2 capture techniques involves the use of solid materials that lack sufficient stability for repeated use or liquid adsorbents that are expensive and require significant amounts of energy. Keywords: greenhouse gases, carbon capture, solid adsorbent, HAS material

Sep 1, 2012

By K. Lillkung

The use of secondary sources has become a very attractive option in the production of platinum group metals as the demand for these metals has increased. One of the promising sources are the spent catalysts, which provide an attractive source as they have relatively high metal content compared with the ores where the metal is originally extracted from. The concentration of platinum group metals in catalytic converters is in the range of 0.1-1 mg/g as the concentration in ores is usually less than 10 ppm. Aqueous chloride solutions are claimed to be a cost effective way in which platinum group metals can be brought into solution and concentrated. In this work the effect of different parameters on the dissolution rates of Pt, Pd and Rh were investigated. The parameters investigated were the Cl- concentration, the temperature and applied potential. Chloride concentrations used were 62.5, 90, 125 and 250 g/l. Temperatures were 25, 40, 60, 80 and 94°C. Potentials were 950, 1050, 1150 and 1250 mV vs. SCE for Pt and Rh and 380, 410, 440 and 470 mV vs. SCE for Pd. Dissolution rates were calculated from the current densities determined by potentiostatic measurements. Thin wire electrodes were used in the measurements. As expected, higher temperature, higher potential and higher chloride content generally increasedthe dissolution rate. However, the effect was nonlinear and slightly different for different metals. The results show that strongly oxidizing conditions are needed in order to achieve reasonable dissolution rates. With the highest chloride content and at potential of 1250 mV vs. SCE and 94°C the dissolution rate of Pt was nearly 1 mm/h, whereas in similar conditions Rh achieved a rate of only nearly 100 µm/h. Similarly, with the highest chloride content and at potential of 470 mV vs. SCE at 94 °C the dissolution rate of Pd was nearly 1 mm/h. Keywords: Pt, Pd, Rh, redox potential

Sep 1, 2012

By A. V. Kurkov

The secondary action reagents (SAR) are organic diphilic compounds capable of altering ac-id-base and donor-acceptor properties of the main collector and consequently the energy of collector interaction with the mineral?s surface, its hardness and fixation forms ratio through associates formation via the hydrogen bonds. When the basic flotation conditions are being established, convergence of the electronic structure of the collector and the mineral being extracted due to minerals surface preconditioning with modifiers and the most efficient collector choice. At the next stage of the selective flotation condition establishment SAR is selected for a more precise adjustment of the energy of the collector fixation on the mineral. Such an approach makes it possible to solve efficiently various issues of flotation separation of non-sulfide minerals. In particular neutral organic substances containing groupings C==O, S==O, P==O (ethers of carboxylic and phosphonic acids, amides of carboxylic, phosphonic and sulfonic acids) were proposed as SAR. In order to enhance the flotation process selectivity in the conditions of water recycling including the selectivity of carboxylic collectors especially in the environment of high hardness water flotation, it was proposed to use SAR with long hydrocarbonic radical and groups with enhanced electronic density within the molecule: N-methylolamides of alkylphosphoric acids and ethers of methylphosphonic acid. Introduction of small amounts of these compounds alongside with the main fatty-acid collector enhance the performance of fatty-acid flotation of fluorite, beryl, columbite etc., lowers the collector consumption, and completely compensates the depressive effect of recycled water. Di-2-ethylhexyl ether of methylphosphonic acid?CH3P(O)(OC8H17-i)2 (hexarane) was more thoroughly researched as such an agent within fatty-acid flotation process. Following aspects of the flotation system were studied: interaction of oleic acid and sodium oleate with hexarane in the liquid phase (infrared spectroscopy); heat emission under the interaction of hexarane-oleic acid ? sodium oleate ? calcium salts (isoperiboric diathermic colorimeter); colloid-disperse state of the collector influenced by hexarane (nephelometric analysis); dynamics of the mineral surface hydration due to the agents (method of indicator negative adsorption); hexarane effect upon the interaction of fat-ty-acid collector with calcium salts (complexometric method with Trilon-B); floatability of pure minerals (quartz, microcline, beryl, columbite) in Hallimond tube; hexarane effect upon oleic acid (sodium oleate) adsorption (nephelometric method for identification of the residual content of oleic acid and its forms within the solution). Upon the research it can be definitely concluded that the adjusting effect of such compounds as hexarane within the non-sulfide minerals flotation process is mainly determined by their interaction with the main collector both within the pulp and at the mineral surface with associates formation due to the hydrogen bond. The consequence is calcium oleates destruction with the release of the most active collector under flotation in hard water environment which determines the efficiency of hexarane joint application with fatty-acid collector under recycled water supply. Therefore the introduction of the class of secondary action reagents is supported by their operation mechanisms and flotation process function and determines a new approach to the development of efficient conditions of selective flotation separation of non-sulfide minerals.

Jan 1, 2014

By F. Z. Dong

The paper is mainly about a study on the techniques of separating iron from pyrite cinder of a certain sulfuric acid plant in Shandong province. The main components of the cinder are Fe2O3 and SiO2, and the degree of liberation of iron mineral and gangue is very high. So the iron concentrate with higher degree of iron and lower grade of silicon and sulfur can be achieved by reverse flotation. The iron grade of the concentrate reaches 63% and the recovery of iron is no less than 63%. And the most important influencing factor of the flotation is the temperature of the pulp. A better guideline can be achieved by magnetic separation. The cinder is magnetizing roasted for 15 minutes with temperature of 800?, and the concentrate with the iron grade 64%, sulfur grade 0.2% and iron recovery 85% can be obtained by two stage magnetic separation. A rotary kiln has been built to deal with the pyrite cinder, and the result of the industrial magnetizing experiment and magnetic separation is satisfying.

Jan 1, 2014

By Arkady Senchenko

At present, there are different traditional and modern methods for ore grindability evaluation. The correct and rational approach to sampling, testing methods and mill sizing enables one to design a workable technology. This paper contains TOMS institute experience in different grinding indices determination over the last 7 years (SAG Design Test, BWi, CWi, RWi, and other). Mill sizing examples and circuits modeling for the projects in Russia and Kazakhstan are considered. Keywords: ore grindability, SAG Design Test

Sep 1, 2012

By C. Y. Sun

China is a country with abundant resources of tungsten, taking one of the world?s top-positions regarding both the total reserve and the amount of industrial production. China?s tungsten resources occur mostly in multi-metallic deposits rather than in single-metallic deposits. China?s multi-metallic tungsten ores have the characteristics of coexistence with other valuable components such as molybdenum, bismuth, copper, sulfur and fluorite. These ores are usually low in grade and difficult to process. The technological challenge in mineral processing lies in separation of multi-metallic components in these complex ores and a comprehensive utilization of natural resource. Several cases of industrial practice of processing China?s typical multi-metallic tungsten ores are presented.

Jan 1, 2014

By G. Pahomova

"It developed an alternative to traditional flotation enrichment refractory of complex lead-zinc ores to obtain conditional lead and zinc products. The scheme involves the use of the processing method of gravitational enrichment of the primary cycle and the combined gravity-flotation-hydrometallurgical in finishing. The method has a high level of comprehensive utilization of mineral raw materials in relation to the elements that are extracted in the process of enrichment in lead concentrate, and the increase in recoverable value of processed ores. INTRODUCTION The primary source of lead are complex sulphide lead-zinc ore, lead ore actually rarer. The value of lead and zinc ores (except lead and zinc) is determined by the presence in them of a wide range of associated components: silver, contained mainly in galena; gold; bismuth in the form of its own minerals, but is associated with galena; cadmium contained mainly in the sphalerite; indium, thallium and gallium contained in sphalerite and galena; selenium and tellurium are present as impurities in the sulfide, tellurium is also found in the form of its own minerals. Of note harmful impurities antimony, which is often associated with lead sulphosalts and arsenic, having a substantially own minerals. By quality (content of lead, or the total content of lead and zinc) lead-zinc ores are divided into rich, ordinary and poor; by oxidation - to sulfide (with a lead oxides content less than 15% and zinc oxide content less than 10%), mixed and oxidized (50% oxide); the latter have a subordinate importance as a source of zinc and lead. Traditionally, the most contrasting technological properties of sulfide ores of nonferrous metals considered flotation properties, which determines the priority in the selection of flotation technology of their enrichment. Other methods of enrichment - gravity (jigging and enrichment in heavy suspensions), radiometric sorting (separation) are used as preliminary operations whose main purpose is to increase the content of lead and zinc in the ore sent to flotation, as well as the removing of part of empty rock in dumping tails prior to flotation. Effective implementation of these methods is possible at large size emphasizing in the ore of lead and zinc minerals, which is typical of the rich ores and which so far mainly worked. At the same time, non-ferrous metal ores (polymetallic, lead-zinc, copper-zinc, etc.) have a sufficiently high contrast to gravitational properties since ore minerals have a higher density compared with a rock minerals. But the gravity of the practice of non-ferrous ores enrichment is not widely used, despite its high degree of environmental safety and lower cost expensive."

Jan 1, 2018