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By H. Matsuoka, M. Kawata, K. Haga, K. Mitsuhashi, C. Tokoro, A. Shibayama, R. Kawarabuki

"The mineral surface characteristic is important for the flotation because it affects the flotation behavior of the mineral. Conventionally, in the flotation process for Cu sulphide ores, the degree of ore floatabilities varies depending on the mineral phase such as chalcopyrite, bornite, or chalcocite. Therefore, mineral surfaces are treated with activators and depressants to control the floatability of target minerals and obtain high recovery performance. There are lots of flotation reagents which have many effects on ores depending on ore characteristics and conditioning methods. For example, sodium hydrosulphide (NaHS) as activator is known to have the effect of resulfurizing and activating oxidized surface of chalcocite and bornite. On the other hand, NaHS is reported to depress chalcopyrite floatability. In this study, the evaluation of mineral surfaces was conducted to predict flotation behavior. Activation of Cu minerals (chalcocite, bornite, and chalcopyrite) by NaHS was experimented. The three Cu minerals were treated in two steps. Firstly, they were oxidized in the drying oven. Secondly, they were treated with NaHS solution. After each treatment step, each mineral was measured by contact angle apparatus then analyzed by X-ray photoelectron spectroscopy (XPS). The results of surface characteristics after oxidation and NaHS treatment were utilized to accomplish the study’s objective. INTRODUCTIONCopper sulfide minerals such as chalcocite (Cu2S), bornite (Cu5FeS4), chalcopyrite (CuFeS2) are well-known abundant copper-containing minerals. Generally, these minerals are recovered and concentrated via collector flotation. In flotation, the wettability of the mineral surface is an important factor in its recovery. When the surface is hydrophobic, the mineral has high floatability and when the surface is hydrophilic, it has low floatability. Usually, Cu sulfide minerals have high floatability. However when their surfaces are oxidized, their floatability becomes lower in flotation. In this case of surface oxidation occurrence, activators are added before flotation to modify the surface property of the Cu sulfide minerals so that they can be floated at a certain flotation condition. Sodium hydrosulfide, NaHS, is known as one of the activators. Zhao et al. (2018) reported that NaHS is often used as sulfurizer for oxidized sulfide minerals (Becker et al., 2014, Clark et al., 2000, Newell et al., 2006, 2007, Newell and Bradshaw, 2007). Although the floatability of Cu sulfide minerals was raised by adding NaHS generally, the results of this flotation study showed that the flotation behaviors of mixed chalcocite, bornite, and chalcopyrite were different. Therefore, it was considered that NaHS works differently for each mineral."

Jan 1, 2018

By Massimiliano Zanin, William Skinner, Owusu Clement, Jonas Addai-Mensah, Daniel Fornasiero

This paper highlights the importance of pulp aeration in the selective separation of chalcopyrite from chalcopyrite/pyrite mixtures of varying pyrite content (20-80 wt.%). Laboratory batch flotation studies and oxygen demand tests were performed to predict the optimum amount of air required for the selective separation of chalcopyrite from pyrite. The pulp oxygen demand was shown to increase with increasing pyrite content but decrease with time as more air is introduced into the system. Complementary batch flotation tests showed significant improvement in chalcopyrite flotation under moderate pre-aeration of the pulp. However, a continuous decrease of chalcopyrite flotation was observed under highly aerated conditions. The amount of air required to achieve maximum chalcopyrite flotation recovery correlated positively with the mass fraction of pyrite in the pulps. The greater the wt.% of pyrite in the chalcopyrite/pyrite pulp, the longer the aeration time required. The optimum aeration time was established as the time before which the oxygen consumption rate constant reaches a bottom plateau. Surface analysis (XPS) indicated that the continuous decrease in pyrite recovery observed with increasing aeration time was due to the formation of more iron oxy/hydroxide on its surfaces, the same species accounting for the decrease in Cp recovery after prolonged aeration.

Jan 1, 2014

By A. Boulton

Low molecular weight synthetic polymers substituted with hydroxyl, carboxyl or sulfonate functional groups were used to improve the flotation separation of zinc or copper sulfide minerals from iron sulfide gangue minerals in three massive sulfide ores of different mineral composition. These polymers produced significant improvements in zinc or copper grades as a result of a selective depression of iron sulfide minerals. It was shown that this selectivity was the result of preferential adsorption of the polymer on the surface of the iron sulfide minerals. The different types of interaction between the functional group on the polymers and the sulfide mineral surfaces could explain the trends observed in the flotation results.

Jan 1, 2003

By L. O. Filipov, N. E. Menad, A. Geneyton

"Zeta potential of synthetic monazites presenting various compositions were measured to investigate the effect of the main lanthanides substitutions on electrophoretic mobility and resulting IEP. The measurements are performed in a CO2 depleted and enriched solutions showing both reduced influence of monazite chemistry and strong influence of ions resulting from the solubilization and dissociation of CO2. The influence of oleic acid on the electrophoretic mobility of those monazites was also investigated. The influence of pH on oleate adsorption was studied using a bubble/particle adhesion system. Adhesion strength measurements were performed on pure synthetic monazite-(Ce) and monazite-(La). An extensive thermodynamic model of monazite in water was developed to highlight correlations between lanthanides hydroxides/carbonates species concentrations in the bulk solution and oleate adsorption. Based on electrophoretic measurements, advanced thermodynamic consideration and adhesion measurements, further details of the oleate adsorption model on monazite surface were proposed.INTRODUCTION Electrophoretic and potentiometric data on monazite and, a fortiori, other rare earth semi-soluble salts such as bastnaesite are extremely erratic (Chelgani et al. 2015). The isoelectric points measured with electrophoretic mobility methods range from 4.7 to 6.5 although sporadic data indicates an IEP (isoelectric point) far from that range. Different explanations are proposed in the literature to explain the IEP variability notably the numerous chemical substitutions that frequently occurred within monazite crystal lattice (Chelgani et al. 2015). Based on lanthanides speciation diagram, several authors highlighted the influence of specific lanthanide species on the flotation performance of rare earth semi-soluble salts when carboxylate or hydroxamate collectors are used. Although lanthanides ions have a great affinity for carbonates groups (Kragten et Decnop-Weever 1987), lanthanide (hydrogen) carbonates were not implemented in speciation diagrams. In this work, an advanced thermodynamic model is proposed to highlight correlation between flotation performance and lanthanide species predominance but also concentrations. Qualitative measurement of the monazite surface hydrophobicity are performed through tests of adhesion of coarse monazite particles onto bubbles. Since flotation and microflotation technics are highly influenced by hydrodynamic parameters, this method was investigated to obtain a sharp contrast between appropriate and inappropriate pH conditions. This paper is to investigate 1) the effect of lanthanides substitution on monazite surface properties through zeta potential measurements, 2) the mechanism of adsorption of carboxylates on monazite surfaces and 3) the effect of CO2 on monazite surface properties and carboxylates adsorption."

Jan 1, 2018

By M. Niinae

Electrokinetic soil remediation by electroosmosis and ionic migration is restricted to soluble sub-stances. At a higher pH, the soil particles sorb more heavy metals, such as cadmium, than at a lower pH and the precipitation reactions of heavy metals are promoted. Both mechanisms make heavy metals immobile, rendering clean up more difficult and electrokinetic extraction inefficient. There-fore, the acidification of soils is very important to increase the clean up efficiencies of heavy metals, such as cadmium by electrokinetic method from contaminated soils. In the present study, acidification of soils and cadmium transport are predicted with a numerical method in which electrical flow is coupled with hydraulic flow, and the sorption process in the soils is induced in the model. The effects of some factors such as electrode configuration, electric field strength and electrode spacing for saturated soils are investigated using this numerical model. The results obtained this study are summarized as follows: The two-dimensional electrode configurations containing cathode surrounded by three or more anodes rapidly acidify the soils and remove cadmium from soils compared with one-dimensional electrode configuration. However, two-dimensional electrode configurations develop spots of inactive electric field between cathodes. A larger electrode spacing increases the processing time required, and it was also found that a larger electric field strength reduced the processing time required.

Jan 1, 2014

By Kang N. Zhong, Hui H. Luo, Yi H. Wei, Yu L. Wang

"More than 85% of phosphorous reserves in China occur as middle-low grade phosphate of sedimentary origin. The main gangues are dolomite, quartz, silicates, and clays. The characteristics of minerals are finely disseminated. Flotation results have shown that the floatability of apatite of this kind of ore is much worse than that of igneous and metasedimentary origin because of its high specific surface area. Although some effective depressants, such as naphthalene sulfonate and phenanthrene sulfonate, are used to decrease the MgO content in the P2O5 concentrate, its presence is still high (about 2%) in the Chinese concentrates. Meanwhile, the wastewater may cause some environmental problems. Batch flotation results and measurements of specific surface area and CO3 2- have revealed that there is a relationship between the floatability of apatite and the surface area.A two-stage flotation flowsheet, which includes a combination of direct and reverse flotation, was developed for beneficiating sedimentary phosphate ores. The direct flotation was conducted in an alkaline medium and most of the apatite and carbonate minerals floated leaving quartz and siliceous gangue in the sink. In the reverse flotation circuit, the floated product was further beneficiated in an acidic medium to eliminate the carbonate as a float product. Apart from the high quality of concentrate, the two-stage flotation also facilitated the treatment and the recycling of wastewater. A wastewater recycling procedure was developed and tested in a continuous flotation process. The key factor was the careful selection of effective and non-toxic reagents."

Jan 1, 2003

By L. Ya Agapova

Emissions from pyrometallurgical processing of copper concentrates are usually subjected to wet scrubbing. The washing sulphuric acid so produced contains up to 0.2 g/L of rhenium, which is recovered by solvent extraction in the form of crude ammonia permeate (NH4ReO4). The mother liquor, obtained from the sulfuric acid wash, contains up to 35 g/L of rhenium and significant amounts of impurities. Crude rhenium salt is commonly processed by double recrystallization to produce marketable salt. A ton of high grade NH4ReO4 can be produced using 3.0-3.5 m3 of mother liquor. We propose an efficient technology of mother liquor pre-treatment aimed at removal of water-soluble organics with subsequent electrodialysis. Electrodialysis of mother liquor in a multichamber electrodialyzer resulted in the production of pure rhenium acid, from which a marketable NH4ReO4 is precipitated using ammonia solution. Multiple steps of recycling consisting of dissolution of NH4ReO4 salt, rhenium acid production from NH4ReO4 salt by electrodialysis and precipitation of NH4ReO4 from rhenium acid made it possible to upgrade the purity of obtained rhenium compounds by 1-2 orders of magnitude. A rhenium metal powder of 99.997% purity was produced by high-temperature reduction of high-purity NH4ReO4 with gaseous hydrogen. Rhenium metal powder of high purity can be produced from sulfate solutions of NH4ReO4 by non-platinum anode-based membrane electrolysis processes also. Keywords: rhenium, mother liquors, membranes, electrodialysis, rhenium acid, ammonia perrhenate, reduction, powder, electrolysis

Sep 1, 2012

The Sydvaranger magnetite mine was shut down in 1996 due to low iron ore prices. It was reopened in 2009. The flowsheet has remained more or less as in the old plant, based upon two grinding steps followed by magnetic separation. The Sydvaranger magnetite is free of harmful elements and should therefore be sold on the high quality market. This requires a concentrate containing less than 2 % SiO2. In the old plant, this grade was achieved by amine flotation. Amine was preferred as collector because it could be used in process water from the sea. The use of amine has been restricted by the Norwegian pollution authorities during the time the mine was shut down. Test work to replace cationic with anionic flotation is therefore done. Research on activation of quartz with Ca or Mg ions prior to anionic flotation was shown by basic research in the period from 1960 to 1980 to be effective under simplified laboratory conditions. This old research has now been followed up from a practical/empirical point of view. The basic work was mainly done on quartz and iron minerals only. In this case, an actual feed containing a number of minerals common in iron ores is used, in order to demonstrate that a commercial process is possible. Calcium activation is shown to work excellently but requires too high pH to be environmentally and economically attractive. Magnesium activation is a more difficult process, because the maximum concentration of MgOH+, which was shown to be the activator, is about 100 times lower than the alternative CaOH+. Flotation success depends partly upon the ore, some amphibole minerals are more difficult to float than pure quartz. Ordinary batch flotation test work is time consuming. A South African microflotation test cell has shown promise, because work can be focused upon flotation of the more critical coarser fractions of the Sydvaranger ore. Keywords: iron ore concentration, anionic flotation, mineral activation, microflotation, Sydvaranger

Sep 1, 2012

By Darryel Boucher, Raymond Langlois, Neil Rowson, Kristian Waters

The Knelson Concentrator is a centrifugal gravity concentrator composed of a high speed rotating bowl into which a mineral slurry is fed. The rotational motion creates a centrifugal acceleration up to an equivalent of 200 G. Under this acceleration, particles enter fluidised riffles along the side of the bowl, with the fluidisation allowing for the substitution of dense material for less dense. The separation mechanism is not fully understood and questions remain on the optimal residence time, slurry feed parameters and bowl surface profile to achieve a better separation. The positron emission particle tracking (PEPT) technique has been applied to record the motion of a -1700+1180 µm particle of a quartz-gold matrix, labelled with 18F radioisotope while it undergoes concentration inside a 3" laboratory scale Knelson Concentrator (KC-MD3) operated at 60 G. The slurry used was composed of quartz and magnetite. Particle trajectories during the first stage of the concentration process where the heavier particles centrifuge through the increasingly dense slurry towards the riffles of the bowl are shown with respect to time. This work reveals new information on particle motion inside the Knelson Concentrator and the results will be used for validation of developed separation model as well as optimisation of a centrifugal concentrator’s performance.

Jan 1, 2014

By A. P. Purgin, M. G. Viduetsky, I. F. Garifulin

"The combined treatment process for mine, tailings storage facility, quarry, circulating, and waste water in the mining and metals industry brings together the conventional chemical treatment processes and pneumatic flotation cells of the KFM series. The key principle of the process is preparing the water for treatment by saturating with finely dispersed air bubbles in the flotation cell blowers. Gas-air lift dispersers located in the lower part of the cell body additionally saturate the cell’s contents with finely dispersed air. Due to the residual content of flotation agents in the treated water, hydroxide ion-air aggregates form at the aerator outlet, supporting the efficient precipitation of hydroxide ions of heavy non-ferrous metals, calcium and magnesium ions. This process was tested in the pilot plant KFM-180 with a raw (untreated) water capacity of up to 18 m3/h per 1 m3 of the flotation cell volume using a mixture of the tailings storage facility and mine water from JSC Safyanovo Copper. The treatment process included raw water treatment with lime, aeration in KFM cells, and filtration in a sorbent bed. The content of metal ions in the treated water is lower than in the feed water by a factor of up to 170,000 and approaches the standards: aluminum 0.016-0.02 mg/l, copper 0.0043-0.0045 mg/l, zinc 0.049-0.052 mg/l. circulating water of Soryin Tailings Storage Facility at JSC Svyatogor. The treatment process included raw water treatment with lime and alkali, aeration in KFM cells, and filtration in a sorbent bed. The content of metals in the treated water is lower than in the feed water by a factor of up to 9000: copper 0.022 mg/l, zinc 0.012 mg/l, iron 0.012 mg/l, manganese 0.015 mg/l, nickel 0.132 mg/l, arsenic 0.016 mg/l. Water hardness is significantly lower: calcium - 12.6 mg/l, magnesium - 1.1 mg/l. This process can be used in the treatment of mine, quarry, tailings storage facility, and circulating water at mining and non-ferrous metals projects."

Jan 1, 2018

By E. A. Bekchurina, Yu. P. Morozov

"This paper presents the results of a study of the concentration of flotation froths in tapered chutes. The tests were conducted on lab and full-scale plants, and the results obtained were mathematically processed. The kinetics of monophase recovery from a stationary flotation froth, hydrodynamics of froth flows traveling in a tapered chute were investigated. The effect was studied of the mass fraction of the valuable component in the chute feed, yield of the chute’s overflow, and chute design on the concentration performance. Processing of the collected data revealed the general laws of the process and allowed to develop a technique for modeling concentration of the flotation froths of sulphide copper ore in a tapered chute to predict the performance without testing. It was found that concentration in tapered chutes allows to obtain products that are comparable in quality with froths after one or several cleaner flotation stages.INTRODUCTIONThe present production expansion rates require continuous improvement in the grade of flotation concentrates, while the grade of the mineral feed is constantly deteriorating. This leads to a significant complication of flotation flowcharts. Flowcharts become multi-staged with multiple cleaner flotations, negatively affecting the production costs.In recent years, researchers are paying close attention to the processes occurring in the froth layer in the flotation cells. Improving the concentrate grade is facilitated by secondary concentration of minerals in the froth layer, which consists in fixing the hydrophobic particles released as a result of the coalescence of the bubbles of the upper layer when moving downward at the liquid-gas interface of the froth layer. In this case, the released hydrophilic particles, trapped in the froth layer as a result of mechanical removal, migrate from the froth together with the liquid phase."

Jan 1, 2018

By David Dreisinger

"The leaching of base and precious metal ores and concentrates continues to progress in both laboratory study and industrial application. These developments are being driven by the need to respond to difficult ores and concentrates that are not amenable to conventional treatment. In many cases alternatives are being developed to conventional treatment (e.g. Pyrometallurgy) for technical and economic reasons.In this paper, a brief general review of some new developments in leaching will be followed by a more detailed explanation of three process developments that have either been industrially applied or are expected to be applied in a short time frame. The three processes to be reviewed in detail are the Mt. Gordon Copper Process, the Anglo American Corporation/University of British Columbia Copper Process and the PLATSOL Process. These leaching processes operate at low (90°C), medium (150°C) and high (220°C) temperature and are successful in quickly and completely extracting metal values from ores and concentrates."

Jan 1, 2003

By Harri J. Lehto, Marja I. Oja

Empirical models used for predicting the performance of screens on the basis of capacity, cut size, water split and grade efficiency curves were evaluated. This paper reports experimental results obtained with single-deck Derrick screens. The performance of the screen was tested with limestone in a separate screen set-up, in a pilot plant and in industrial scale test runs. The results of pilot plant experiments showed that the measured water split was higher than the measured bypass. This is an indication to that water flow does not entrain the same proportion of all fine particles present in the feed which is advantageous for screening. The experimental design for the industrial test runs was made on the basis of the pilot plant tests. Suitability of the existing models has been checked and accuracy compared. The tests showed that best grade efficiency model was the Rosin-Rammler model. An empirical model for the evaluation of the model parameters as a function of pulp density of the feed and the load of the screen is suggested.

Jan 1, 2003

By Behzad Vaziri Hassas, Firat Karakas, Mehmet Celik, Onur Guven

Since dewatering is a costly process, removal of moisture from relatively fine size lignites is an important industrial problem. As the lignite gets finer, the presence of micropores and relatively low hydrophobic nature of lignite lead to trapping of large quantities of water in the coal matrix. Lignites used in power stations need to be dried to a certain degree of humidity before it is transferred to the combustion chamber. It is generally wise to dewater coal as much as possible by physical means before it is dried. However, dewatering cost in some cases may be prohibitive. Thus, sometimes removal of even little percent moisture may be of great help in such operations. Surfactants have been used to increase the efficiency of coal dewatering. It is crucial to select appropriate type and amount of surfactants in order to get higher efficiency. Since the hydrophobic characteristic of coals increases with increasing the coal rank, dewatering of bituminous and anthracite can be accomplished using low HLB surfactants (Oily), however, these surfactants are not efficient in the case of low rank coals like lignites and brown coals. It is suggested that adsorption of low HLB surfactants on high rank coals is governed by Acid-Base interactions rather than electrostatic and van der Waals forces. Since this characteristic in lignites is not strong enough, low HLB surfactants could not be effectively adsorbed on low rank coals to make surface more hydrophobic. In this paper, a special set-up has been designed to study the effect of high HLB surfactants on dewatering of fine lignite particles. It is shown that high HLB surfactants function more efficiently on low rank coals than low HLB ones.

Jan 1, 2014

By Tchingis Lekhatinov, Lev Filippov, Vyacheslav Severov, Alexandre Matinin, Victor Samyguin, Inna Filippova

"Comparison of flotation efficiency of the new multi-zone flotation cell (MZFC) and different conventional cells was carried out at lab and pilot scales on the various samples: high contrast pyrite tailings and old copper containing tailings. MZFC is a cell of intensive flotation, which provides optimal hydrodynamic conditions for all flotation sub processes. Enhancing of particle attachment, creation of conditions for coalescent flotation, selection of spatially separated zones according to optimal hydrodynamic conditions for flotation sub-processes are proposed as main principles to design an MZFC. The bubbles/pulp stratification was pointed out as a limiting step in the existing intensive flotation machines. Two strategies to improve bubbles/pulp stratification in the MZFC were studied: (a) impact of pulp-bubble jet to the surface of a prismatic insert inside of cell, which provides the detachment of low hydrophobic particles from bubbles, and (b) profiling the pulp/bubbles jet from the reactors due to a specific geometry of cell walls. The new continuous MZFC devices were demonstrated similar or higher efficiency in comparison with laboratory batch flotation cells for pyrite flotation. Higher flotation efficiency (82%) with pure pyrite concentrate (51.2% of sulfur) and a recovery level of 92% was obtained in MZFC when the cell with stratification by impact was used. Similar results were obtained with old Cu-containing tailings. Although MZFC had 1.5 times greater yields of concentrate than a batch flotation cell, it provided the increase of chalcopyrite recovery by 29.4% and concentrate grade by 4.8%. An original organization of pulp/bubbles stratification in the separator part of the new intensive flotation machine using variable geometry inserts allowed the best flotation selectivity with a bubble mineral loading coefficient 1.5 fold higher than the laboratory mechanical or pilot cells."

Jan 1, 2014

By Tatyana A. Ivanova, Tamara N. Matveyeva, Anatoliy A. Fedorov, Tatyana V. Nedosekina, Valentin A. Chanturiya

An ingenious methodology purposively developed by the authors for comprehensive assessment of flotation properties, electrophysical characteristics and. crystal chemistry features of natural gold-bearing sulfide minerals of different origin has been used in this study. Examination of the elemental composition of the minerals, ion-molecular components of the liquid phase in suspensions, surface properties of sulfides and different flotation reagents sorption forms was performed using the methods of X-ray phase and spectral analysis, potentiometry, UV and IR spectrometry, computer image analysis, and computer simulation techniques. The role of isomorphous impurities in the formation of hydrophobic sulfhydric collector layers on mineral surfaces in complex ore processing has been elucidated. The parameters characterizing the variability of the Fe:S ratio in pyrite of different origin have been determined based on non-stoichiometry characteristics of natural gold-bearing sulfide crystals. An ingenious method of formatting and linear approximation of experimental data was used to find out the quantitative relationships between the impurity content, electrophysical characteristics, non-stoichiometry and floatability of pyrite from a number of different deposits. The effect of the impurity species present in sulfides on the characteristic pH value marking the floatability peaks as such and their trend of shift towards higher alkalinity has been revealed. A theoretical substantiation has been given to prognostic assessment criteria for processing characteristics of gold-bearing sulfide minerals with varying composition. New flotation reagents and advanced reagent systems which help to increase the contrast of processing characteristics for different gold-bearing sulfides, resulting in improved selectivity, have been developed. The mechanism of selective flotation of precious metal-bearing Fe and As sulfides achieved by using short-chain dithiocarbamates and a mixture of cyclic trithiocarbonate with oxyalkylsulfides has been analyzed.

Jan 1, 2003

By Fuqiang Zheng, Shuai Wang, Feng Chen, Yufeng Guo, Guanzhou Qiu, Tao Jiang

"The direct reduced iron powder and Ti-V-rich material was prepared from vanadium titanomagnetite concentrate by solid-state reduction-magnetic separation. The result indicated that under the studied conditions, adding KS can effectively improve the metallization rate of pellets. 2% KS was well mixed with vanadium titanomagnetite concentrate to make the pellets. The green pellet was preheated at 900 ? for 6 min. The preheated pellet was reduced at 1050 ? for 100 min, then crushed and ground to more than 80% was below 0.045 mm. The direct reduced iron powder and Ti-V-rich material were separated from the slurry by wet magnetic separation at 800Gs. The TFe content of magnetic material was 90.63%, and the Fe recovery rate reached 96.53%. The TiO2 and V2O5 contents of Ti-V-rich material were 28.40 % and 1.64 %, respectively. The TiO2 and V2O5 recovery rates were 69.05% and 96.82%, respectively. 1. Introduction The ilmenite and rutile are the main titanium resources which can be used in the present technical level and economic conditions[1,2]. However, with the rapid development of China’s economy, the market demand of titanium products is increasing sharply. The current supply of ilmenite and rutile cannot meet the needs of chemical industry[3]. China is rich in vanadium titanomagnetite concentrate which contains abundant titanium and vanadium resources. The TiO2 and V2O5 content of vanadium titanomagnetite concentrate are usually about 7% and 0.3%, respectively[4]. Because the TiO2 and V2O5 grades are low, it generally requires pre-concentrated to Ti-V-rich material before extracting the titanium and vanadium. Therefore, it is vital to find effective processes for pre-concentrating the titanium and vanadium in vanadium titanomagnetite concentrate. There are many methods[5-13] developed or under development to pre-concentrate Ti-V-rich material from vanadium titanomagnetite concentrate, including the blast furnace process, pre-reduction electric furnace process, to utilized vanadium titanomagnetite concentrate are direct reduction-electric furnace smelting, sodium salt roasting-direct reduction-electric furnace smelting and direct reduction-magnetic separation and so on. The blast furnace process and other methods cannot effectively utilize the titanium and vanadium resource due to the technical or environmental problems[9]. In this study, the vanadium titanomagnetite concentrate was obtained from Panxi region of China, the reserves of which account for 11.6% of vanadium and 35.17% of titanium all over the world[3]. The preparation of direct reduced iron powder and Ti-V-rich material based on reduction-magnetic separation is proposed. The process utilizes a new catalyst for titanium ore reduction in rotary kiln followed by magnetic separation. Using this novel technology, the titanium-vanadium and iron are successfully separated. Compared to the traditional reduction of Ti-bearing ore, the reduction temperature reduced to 1050 ?, leading to higher efficiency, lower energy consumption and investment, and broader applications."

Jan 1, 2018

By Katarina Theander, Robert J. Pugh

The generation of froth with a critical degree of stability and height is an important aspect of the froth flotation. In this paper we have studied the synergism and anti-synergism in frothing behaviour in a mixed flotation collector/frother mixture (a model fatty acid; sodium oleate and a model frother; nonionic (polyethyleneoxide alkyl C14E6). Values of the collector / frother molecular interaction parameters (the ß-parameters) were determined from the surface tension data using regular solution theory. The frothing characteristics of the system were evaluated using a glass column equipped with a series of conductivity electrodes, which enabled the water content of the froth to be determined. From these measurements, the dynamic frothability and static froth stability were determined. It was concluded that the synergism/anti-synergism in frothability was depended on the molecular composition of the surfactant system, the diffusion of monomer to the thin film interface and on the breakdown of the mixed nonionic/anionic micelles.

Jan 1, 2003

By B. Vasanthakumar, H. Ravishankar, S. Subramanian, J. Braun

The flotation of sphalerite and galena in the presence of intra- and extra-cellular components isolated from Bacillus circulans before and after adaptation to the chosen minerals has been studied. Based on various biochemical treatments, the key biomolecule primarily responsible for the flotation of sphalerite has been identified as DNA, which functions as a bio-collector. A noteworthy finding is the considerably higher flotation recovery of sphalerite obtained in the presence of single stranded DNA (79.8%) vis-à-vis double stranded DNA (50.2%). Selective flotation tests using the soluble fraction obtained after thermolysis treatment highlight that sphalerite-adapted cells yield a higher selectivity index (S. I.) of 31.2 compared to galena-adapted (S.I. 4.3) or unadapted (S.I. 12.2) cells. During bacterial adaptation to the above chosen minerals, the quantitative and qualitative changes in the surface potential, surface morphology and cell wall components have been monitored. The prior adaptation of the bacteria to sphalerite results in the secretion of a higher amount of proteins, eDNA and phosphate, whereas adaptation to galena leads to a higher amount of polysaccharide, uronic acid and acetylated sugar, vis-à-vis the unadapted bacteria. A significant observation is that the bacteria undergo a change in morphology from rod to sphere as a strategy to resist metal toxicity during adaptation to galena. Interestingly, this phenomenon is not observed during bacterial adaptation to sphalerite. This morphological transition has been shown to involve changes in crucial cell wall components as well as changes in the levels of expression of bacterial cytoskeleton element mreB gene involved in the maintenance of the rod shape. The sequence of B.circulans mreB gene has been identified using Polymerase Chain Reaction (PCR) followed by DNA sequencing.

Jan 1, 2014

By Dingwu Feng, Jannie S. J. van Devente

"The effect of ultrasonication on reactions at solid/liquid interfaces was investigated in two slurry systems, i.e. gold cyanidation and geopolymerisation. The kinetics of gold extraction were significantly enhanced and the cyanide consumption was reduced in the cyanidation of a pyrite concentrate using ultrasonication, probably due to the prevention of leaching passivation, the improvement of the dissolution of the gold host sulphides and the oxidation of soluble sulphides to sulphate. The effectiveness for ultrasonication was improved with the injection of oxygen and the addition of dithiophosphate through enhancing the formation of the oxidation radicals and selectively inducing cavitation bubbles directly at the sulphide interfaces. Ultrasonically enhanced cyanidation could render currently uneconomic deposits viable for extraction by improved cavitation efficiency with the aid of surfactants.Ultrasonication increased the compressive strength of the formed geopolymers through accelerating the dissolution of the Al-Si materials, strengthening the bonds at the solid particle/gel phase interfaces, enhancing the polycondensation process and improving the formation of semi-crystalline to crystalline phases. The use of power ultrasound will yield high-performance geopolymer materials."

Jan 1, 2003