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By P. M. Solozhenkin, V. N. Kovalev

Russia is a global antimony market leader. The three major antimony production provinces are Sakha Republic (Yakutia), Krasnoyarsk Territory and Trans-Baikal Territory. Russia’s largest antimony resources are Zhipkozhinsky and Solonechensky deposits in Sakha Republic (Yakutia) and Olimpiadinskoe deposit in Krasnoyarsk Territory. This work demonstrates the efficiency of computer programs and chemical technology aimed at the study of the behavior of collectors used in the processes of flotation of antimony, arsenic and Au (I – III) minerals. The most promising collectors for the flotation of ores containing antimony and gold on the basis of P(V) and compounds with S, O and N atoms were chosen. The mechanisms of interaction with the mixtures of two or three components of collectors were studied. High recovery of antimony and gold was reached in the processing of Au-Sb ores of Sarulah and Sentachan deposits in Sakha (Yakutia). X-ray radiometric methods of separation of antimony ores of Trans-Baikal Territory deposits were proposed. In order to choose the most cost-effective solvents for hydrometallurgical processing of Sb, Au-containing concentrates the method based on clusters formation between transition solvents and antimony minerals was suggested. The nature of Au losses was theoretically revealed in the sulfide-alkaline process. On the base of computer simulation, the formation of various complexes of (KAu) types was developed, for example, hydrosulphidic gold, thiosulfates of gold - Na3AuS4O6, antimony and arsenic gold, trithiostibate (III) and trythioarsenate (III) KAu were produced. The practice of processing of goldantimony concentrates to produce high-quality antimony trioxide and antimony-gold containing alloy (AGCA) regarding the special conditions of the Far North region, were analyzed. The affinage of AGCA was recommended. Creative project development of antimony industry in Russia in order to produce antimony compounds and pigments, including pyriform compounds and flame retardants (antipyrenes) is discussed.

Jan 1, 2018

By Jacqueline Satur, Yoshiaki Kon, Buenaventurada Calabia, Xiao Sheng Yang, Arvo Naumanen, Kenzo Sanematsu, Sayaka Morita, Tetsuichi Takagi

Granite ores are composed of silicate minerals and a variety of valuable REE (rare earth elements)-bearing minerals, however the processing technique to recover these valuable minerals is not yet developed. In this study, the recovery of REE-bearing minerals by dry magnetic separation and wet high intensity magnetic separation (WHIMS)-settling from surface sample and from drill core sample, respectively, of a granitic REE-Zr-Nb ore deposit was investigated. The two samples have different mineralogy however in both samples, light REE are commonly contained in REE carbonate minerals while Y and heavy REE are commonly contained in zirconium silicate minerals and pyrochlore. The liberation size of the REE-bearing minerals in the two samples ranges from 10-250 ?m. Previous flotation testwork conducted on the drill core sample reported high recoveries of La2O3 (88%) and Ce2O3 (88%) but low recoveries of Y2O3 (42%), ZrO2 (17%), and Nb2O5 (29%). The objective of this study was to obtain higher recoveries of Y2O3, ZrO2, and Nb2O5 by dry magnetic separation and WHIMS-settling. Both processes implemented the application of a low magnetic intensity to initially separate the ferromagnetic minerals then a high magnetic intensity to recover the REE-bearing minerals. The results showed higher recoveries of Y2O3, ZrO2, and Nb2O5 by dry magnetic separation and WHIMS-settling indicating the potential of magnetic separation and gravity separation in recovering the heavy REE-bearing minerals. WHIMS-settling is more recommendable than dry magnetic separation because of its applicability in treating a wider range of particle size. In the WHIMS-settling, the light REE, Y, and Zr minerals were recovered mainly by applying four stages at high magnetic intensity of 21,500 gauss while the weakly magnetic pyrochlore was recovered mainly by decantation of the nonmagnetic slurry after a short settling time of 0.25 to 0.50 h. (MAX.300 words)

Jan 1, 2014

Much has been published in recent years on the challenges facing the engineer of the 21st century and the consequent challenges facing the education providers and industry. The world is changing rapidly on the social, economic, political, technical and environmental fronts and our metallurgists/mineral processing engineers of the future will arguably need to have a different set of skills than those which were traditionally regarded as adequate during the latter half of the 20th century. This paper attempts to explore some of these issues and their ramifications.

Jan 1, 2014

By D. J. Zhao

The reduction of ilmenite pellets was investigated at 950°C and 1000°C under a CO-N2 gas mixture with 10 L/min gas flow rate. All the reducing reactions were conducted in a furnace with a thermogravimetric analysis system. The reduction rate is higher at 1000°C than that at 950°C. At the early stage of the reactions, with the CO concentration increasing in the gas mixture, the reduction rate increased at 1000°C. In addition, at the early stage of the reactions, a rapid temperature increment and a rapid conversion of oxygen were observed on the curves of temperature versus time and conversion of oxygen versus time under different experimental conditions. The solid reaction products obtained in these experiments were analyzed by Scanning Electron Microscopy (SEM) and Energy Dispersive Spectrometers (EDS). Metallic Fe with small amount of Ti dissolved in it and oxides of Ti were found in the solid reaction products, but the formation of any nitride phases was not found under the prevailing conditions.

Jan 1, 2014

By Jurgens J. Louw, Vincent C. Smith, Gareth C. Smith, Agit Singh, Dave G. Hulbert

"The flexibility of the PlantStar control platform has enabled Mintek to investigate and easily develop new control strategies for both milling and flotation. This includes a Solids Feed Controller, a Safety Limit Controller, Mill Power Optimiser and Flotation Optimiser, amongst others.The solids feed controller was developed for minerals processing plants using a specialised time delay compensator. Using conventional time delay compensators that are purely model based, results in robustness problems due to model uncertainties. The Mintek Solid Feeds Controller makes use of a plant model, but compensates for model inaccuracies, giving more controller stability and a more robust delay compensation algorithm.The safety limit controller has been developed to switch smoothly between normal and safety control loops without bumping the process. The safety loop output is chosen in accordance with a predefined list of priorities and whether the respective constraint boundaries are exceeded.The Mill Power Optimiser helps to find the power peak on the mill power curve. This insures maximum grind with maximum throughput. It also prevents power dips due to mill overloads, making the milling circuit easier to operate.The flotation optimiser algorithm analyses trends of all accessible variables in the process. The algorithm uses this information to calculate operating conditions that will control the residence times, mass pulls and circulating loads within a flotation circuit to a specified setpoint. Research is being done to now optimise these setpoints in order to achieve better recovery."

Jan 1, 2003

By Kr. J. Dedelyanova

Selective flocculation of iron minerals could improve the economics of high intensity magnetic separation as concomitant process. When the minerals are finely disseminated is necessary a finer grinding to be applied which generates a lot of slimes. The HIMS is not enough efficient for particles below 20 microns ? territory where the selective flocculation is already well known industrial practice, so the combination of these two methods of beneficiation can bring a higher grade at high recovery to be achieved. The dynamics and selectivity of the precipitation process is studied in batch tests with flocculant starch and dispersants sodium silicate and sodium hexametaphosphate. The influence of preliminary conditioning with nitrogen acid at pH 2 before flocculation is also investigated. Flowsheet including these two methods is tested and the distribution of iron is shown.

Jan 1, 2014

By Ata Akcil, Z. B. Karshigina, Ye. G. Bochevskaya, E. A. Sargelova, Z. S. Abisheva

Phosphorus slag is one of the most large-tonnage of yellow phosphorus production waste, which for decades stored in the slag disposal, by polluting the environment and creating environmental problems in the regions. Phosphorus slags from the processing of Karatau phosphorites are a very promising source of raw materials not only for silicon compounds but also rare earth metals (REM). Among the REM, yttrium, neodymium, europium and lutetium predominate, which are relevant to high-tech industries. The report presents technological scheme of complex processing of slags of phosphoric production with obtaining of REM concentrate and precipitated silicon dioxide ("white soot"). The regime parameters of the main operations of the technology are determined: I stage- leaching of slag with nitric acid solution; extraction of the REM-containing solution with tributyl phosphate and stripping of the REM with water; settling of solution of salts of oxalic acid, calcining the precipitate to obtain a concentrate S REM oxides and II stage of leaching silicon cake to obtain "white soot". Recovery of S REM from slags of phosphoric production on various redistribution has made, %: leaching – 95.0; extraction - 90.2; extraction on the average ~ 93.2; the production of a concentrate of REM oxide is 93.9. A concentrate containing 17.3 % of REM oxides was obtained. According to X-ray analysis it contains the following phases: calcium oxide, portlandite2, gadolinium oxide and yttrium, gadolinium oxide, gadolinium oxide and cerium, neodymium oxide, neodymium oxide and cerium. Thus, the concentrate can serve as a raw material for the production of individual rare-earth metals like gadolinium, cerium, yttrium and neodymium. After performing the II stage of leaching siliceous cake with nitric acid the samples of "white soot" were obtained. Its chemical composition corresponds to the state standard and has a specific surface area equal to 180 - 200 m2/g. The technology has been tested in a large-scale laboratory scale and will solve the problem of complex processing of phosphorus raw materials and import substitution in Kazakhstan. The end-to-end recovery of S REM oxides and silicon into concentrate and product from their initial content in slags is ~ 75.0 and 98.0 %, respectively.

Jan 1, 2018

By Zhu Yangge, Hu Xiaoxing, Feng Qiming, Zhang Guofan, Zhang Xingrong

"During the flotation process of ilmenite and titanaugite with fatty acid as collector, unavoidable ions such as Ca2+, Mg2+, Al3+, Fe3+ and Fe2+ demonstrate considerable influence on the floatability of the minerals. In this study, flotation test, zeta potential test, and solution chemistry calculation were adopted to investigate the mechanism of how these metal ions affect the floatability of ilmenite and titanaugite in different pH conditions. The results show that in weak acidic solution, Ca2+ and Mg2+ mainly freely exist in the solution with little adsorption on mineral surface, and their reaction ability with oleate ions is weaker than active site on ilmenite surface (Fe), thus they show negligible effect on the flotation of ilmenite; Al3+ shows similar reaction ability with oleate ion compared to Fe3+, which lead to competitive reaction with collector, so the flotation of ilmenite is depressed. While Fe3+ can adsorb on surface of titanaugite in the form of Fe(OH)3, and it shows stronger reaction ability with oleate ion compared with active site on titanaugite surface (Ca and Mg), which proves an activation effect on titanaugite flotation. In alkaline solution, all these five kinds of ions can adsorb on titanaugite surface, and the floatability of titanaugite will be activation. Based on the above analysis, it can be deduced that in the flotation system using fatty acid as collector, the adsorption of metal ions on mineral surfaces and the stronger reaction ability with collector than active site on mineral surfaces, are the two prerequisites for metal ions show activation effect on mineral flotation.INTRODUCTIONIn flotation pulp, the existence of metal ions is often inevitable. There are two sources for these metal ions: the first part is generated in grinding and flotation process due to the oxidation, reduction, corrosion or dissolution of minerals or grinding medium; the second part is from the flotation water or the addition because of the technology need. The metal ions in the pulp have a considerable influence on mineral flotation. Earlier researches are focus on the activation effect of mineral floatation by metal ions to obtain a higher flotation efficiency, many effective activators were found, such as Cu2+ activated sphalerite, Pb2+ activation wolframite, and Ca2+ activation quartz flotation, these metal ions have become the commonly used activators in industrial production. And many studies attempted to explain the mechanism of how metal ions affect the floatability of minerals. James (James et al, 1972) suggests that metal hydroxide precipitation is the main component leads to activation effect, while the study of Fuerstenau (Fuerstenau, 1976) showed that the metal ion hydroxyl complexes played significant role. In recent years, the reuse of mineral processing wastewater has attracted more attention (Rao et al, 1989; Liu et al, 2013; Wang et al, 2014), as a main component in flotation wastewater, the influence of “unavoidable ions” on flotation process still need in-depth study."

Jan 1, 2018

By F. K. Ikumapayi

An approach to environmental sustainability and improved process economy, in sulphide minerals production is recycling of process water in flotation of complex sulphide ores, although the chemistry of process water may be a critical issue to flotation efficiency. The influence of major components of calcium and sulphate ions in process water on xanthate collector adsorption and flotation response using pure chalcopyrite, galena and sphalerite minerals were investigated by Hallimond flotation, zeta-potential measurement, FTIR and XPS spectroscopy studies, while bench scale flotation tests were also carried out using complex sulphide ores. The impact of the species in flotation was comprehended using deionised water, tap water, process water and simulated water containing equivalent amount of calcium and sulphate species in process water. Hallimond flotation results showed a decrease of chalcopyrite and galena recovery in process water and also in the presence of calcium and sulphate ions in both deionised and process waters, whereas sphalerite does not respond to flotation. The adsorption of calcium and metal ions but not sulphate ions on the minerals is evidenced by zeta-potential data. FTIR and XPS studies revealed the presence of surface oxidized sulfoxy species and surface calcium carbonates on chalcopyrite in the presence of process water and water containing calcium ions, surface oxidized sulfoxy and carbonate species on galena in the presence of deionised water, process water and water containing calcium and sulphate ions, all at flotation pH 10.5, and these surface species influenced xanthate adsorption. The presence of surface oxidized sulfoxy and carbonate species at the sphalerite flotation pH 11.5 were seen in the presence of deionised water, process water and water containing calcium and sulphate ions, but the surface species does not influence xanthate adsorption. Bench scale flotation using two different complex sulphide ores showed that chalcopyrite, galena and sphalerite recoveries are better in process water than tap water. The studies showed that the process water can be recycled in flotation with no detrimental effect on grade and recovery of sulphide minerals. Keywords: sulphide minerals, flotation, zeta-potential, FTIR, XPS

Sep 1, 2012

By Sarra Scherbakova, Alexander Kurkov, Andrey Egorov

"Deep concentration of iron ores involves extraction, in addition to magnetite concentrate, of hematite and martite concentrates and recovery of other valuable components. A flotation technology was designed specifically for finely disseminated hematite ore, allowing producing saleable hematite concentrate containing 64-66% Fe. The main process challenge is caused by the presence of other ferruginous minerals such as carbonates, silicates, and phosphates, and fine hematite and martite mostly concentrated in the -0.044 mm fraction. Main operations of the processing circuit are removal of slime, flotation to remove impurities (carbonates, phosphates etc.) with an anionic phosphorous collector in an alkaline environment, hematite and martite flotation using same collector in a slightly acidic environment to produce commercial iron concentrate. Tailings of wet magnetic separation of magnetite containing 24.5% Fe and finely disseminated hematite ore containing 51% Fe were processed to produce iron concentrates with a yield of 15% and 50%, respectively, containing approximately 65% Fe and 5% of silica. Hematite flotation tailings had the highest content of gold (up to 0.09 - 0.11 g/t), while in other products it never exceeded 0.02 g/t. Using a Knelson concentrator was able to recover 40 to 45% of the gold into 3.31 g/t Au gravity concentrate. The success of gravity concentration is due to high gravitational contrast of gold to mostly quartz and aluminosilicates in the hematite flotation tailings. In general, the proposed process can be used as a solution to the challenge of selective concentration of finely disseminated iron minerals."

Jan 1, 2014

By Ronel du Plessis, John C. Davidtz, Jan D. Miller

Recent results from electrochemical measurements demonstrate that trithiocarbonate (TTC) collectors are more readily oxidized to their corresponding dithiolates than the dithiocarbonate/xanthate (DTC) collectors. Based on the traditional analysis of collector adsorption, trithiocarbonates might then be expected to be effective for bulk sulfide mineral flotation. Previous bench-scale flotation research had shown that TTC collectors are very effective for the flotation of copper sulfide minerals and PGM (platinum group metal) sulfide minerals. More recently, the TTC collectors were evaluated for auriferous pyrite recovery in benchscale plant scale flotation testing in the United States and in plant tests at Anglogold in South Africa. TTC collectors were also applied in bench-scale testing of a PGM ore. In each case an improved separation efficiency was realized. Fundamental studies at the University of Utah examining the effect of collector structure (functional group, -O-CS2 versus .S-CS2), specifically with respect to auriferous pyrite flotation, are in progress. The effect of collector structure was evaluated with air as well as nitrogen as the flotation gas medium. Experimental techniques utilized included electrochemically controlled contact angle measurements to evaluate mineral hydrophobicity and infrared spectroscopy to explain collector adsorption phenomena at the mineral surface.

Jan 1, 2003

By Z. Hu

A complex polymetallic sulfide ore in Yunnan, China, has various valuable minerals, which are Chalcopyrite, Galena, Pyrite, Gold, Silver, and Magnetite. A reasonable new flowsheet with a bulk flotation and a flotation separation of sulfide minerals that are Chalcopyrite, Galena, and Pyrite was carried out at first stage. After that tailings were treated by low intensity magnetic separation to achieve magnetite concentrate. A high Pb concentrate assaying 60.00 percent Pb at total recovery of 75.71 percent with 40.50 g/t Au and 1390.00 g/t Ag, a final high Cu concentrate assaying 24.45 percent Cu at high recovery of 92.03 percent and a magnetite concentrate assaying 60.78 percent Fe at recovery of 33.61 percent with 18.45g/t Au and 234.99 g/t Ag, are obtained. The total recovery of Gold and Silver in Pb concentrate and Cu concentrate reached 71.63 percent and 67.32 percent, respectively. It is shown, that this new flowsheet could realize efficient recovery for all of the valuable minerals in the ore and is easy to be industrialized. Keywords: bulk flotation, magnetic separation, polymetallic sulfide ore, depressant

Sep 1, 2012

By John O. Marsden

"Technology development and innovation has played a crucial role in the copper industry throughout history. The effective development and implementation of new technologies allows mankind to produce copper at progressively lower cost of production at a given feed grade and mineral type. This progress serves to counteract cost inflation/escalation over time and, depending on the magnitude of the cost benefit, allows ore cut off grades to be reduced thereby improving the availability, accessibility and utilization of resources. Two broad categories of technology development and innovation play a key role in this process: (i) incremental improvements and optimization of existing technology provide benefits in the near- to medium-term, and (ii) step change technologies provide value over the longer term. A key issue for potential developers and implementers of new step change technology is how to justify resource allocation and expenditures for such initiatives. This paper examines this issue with reference to specific case studies in the copper industry. INTRODUCTION AND BACKGROUND Technology development and innovation has played a crucial role in the commodity minerals industry throughout history, and none more important than the copper industry. As new, cost-efficient technologies are commercialized, the cost of production in real terms at a given ore feed grade and mineral type decreases. This progress enables ore cut off grades to be reduced allowing lower grade material to be processed economically, which in turn increases the availability and supply of the metal or mineral of interest. Cost inflation/escalation works in the opposite direction, squeezing margins for operations utilizing incumbent technology to process material from a given ore deposit. A prior review by the author considered the issue of technology development and sustainable competitive advantage. This review concluded that first movers and fast followers can achieve competitive advantage for periods of 10-15 years through effective deployment of new technologies (Marsden, 2004). A new, more comprehensive study and evaluation was completed in 2014. This paper presents a portion of the results from the 2014 study."

Jan 1, 2018

By O. Celep, H. Deveci, Ersin Y. Yazici, F. Ahlatci

"There are increasingly stricter environmental regulations imposed for use of cyanide leaching for the extraction of gold from ores. Alternative lixiviants to cyanide, preferably with low toxicity, have been extensively studied. Thiosulphate has emerged as one of the most suitable alternative leaching agent in place of cyanide due to its low toxicity and technical attributes e.g. fast leaching kinetics, high gold extractions from carbonaceous ores in particular. High solubility of most copper minerals in cyanide solutions results in low gold extractions due to excessively high consumption of cyanide. In contrast, low reactivity of copper minerals in thiosulphate solutions makes thiosulphate leaching potentially suitable alternative for treatment Cu-bearing gold ores. The extraction of gold/silver from a copper-bearing pyritic gold concentrate (62 g/t Au, 110 g/t Ag and 0.3% Cu) in thiosulphate solutions was investigated in this study. The concentrate is composed of predominantly quartz (25%) and pyrite (32.7%) as well as sphalerite (5.37%), galena (2.12%) and anglesite (1.13%). Other minor minerals are arsenopyrite, chalcopyrite, covellite and bournonite. Previous studies by the authors indicated that the concentrate did not respond well to cyanide leaching (i.e. 45-46% Au/Ag at 1 g/L NaCN). The effects of concentration of ammonia (0.2-1.5 M NH3), thiosulphate (0.1-0.75 M S2O3) and copper (0-20 mM CuSO4) on the extraction of gold and silver over 8 h. was investigated. Increasing the concentration of thiosulphate and ammonia substantially improved the rate and extent of gold leaching while high copper levels produced an adverse effect particularly at low concentration of thiosulphate (i.e. 0.1 M). Complete extraction of gold was achieved under suitable conditions. In contrast to gold, silver extractions remained consistently at low levels (i.e. 28%). These findings demonstrated that thiosulphate leaching could be used to achieve acceptable levels of gold extraction from the copper-bearing pyritic gold concentrate."

Jan 1, 2018

By Y. F. Li

Fengning ilmenite ore is a magnetic deposit in gabbro containing high phosphorus and low titanium, the main minerals in which are ilmenite, magnetite and apatite. The dissemination size of magnetite is so fine that even the percentage of -0.010mm level is up to 36.50%. The fine and vein magnetite are distributed in gangue and ilmenite, so the majority of the magnetite is difficult to be separated from the gangue. Ilmenite is difficult to be recovered by low-intensity magnetic separation even through fine grinding. In high-intensity magnetic separation of ilmenite, the gangue inter-growth with the magnetite and the Fe-containing silicates may be enriched in the concentrate, and the ilmenite of the concentrate will be reduced. Based on the processing mineralogy research, combined gravity-flotation process is suggested to recover the ilmenite. The method is also good to reduce phosphorus in the ilmenite concentrate.

Jan 1, 2014

By C. Dorfling, W. A. Rossouw

"Hydrometallurgical processes used for metal recovery from waste printed circuit boards (PCBs) typically involve dismantling, shredding and physical separation prior to successive leaching stages for selective dissolution of different metals. The principles of the physical separation units are well understood, but valuable metal losses of more than 30 % can be incurred during these processing steps. The impact of the physical separation units’ performance on downstream leaching operations have not been defined; this prevents the development of a well-integrated process. The objective of this project was to determine to what extent the base metal leaching behavior depends on the physical separation pre-treatment. PCBs were shredded to 100 % passing 2 mm before physical separation by dense medium separation (DMS) as well as magnetic separation. Batch leaching tests using various concentrations of sulfuric acid were conducted on three feed fractions: (1) shredded PCBs without any physical separation, (2) heavy fraction recovered from DMS, and (3) non-magnetic fraction recovered from the DMS heavy fraction. DMS increased the metal content in the feed from 48 % to 75 % on a mass basis, but 70 % of the gold and 20 % of the copper reported to the light fraction. The application of magnetic separation to the heavy fraction produced by DMS removed 67 % and 61 % of the iron and nickel, respectively, while negligible amounts of non-magnetic metals were removed. Although DMS successfully concentrated the feed and magnetic separation removed the majority of iron and nickel, these steps did not result in any improvement in the rate or extent of copper leaching. Metals generally leached faster when the sulfuric acid concentration was increased from 1 M to 2.5 M; this effect was seen to be more pronounced for pretreated feed. INTRODUCTION The fast rate of technological development has led to a decrease in the service life of electronic devices. This is resulting in an increased rate of electronic waste generation. The recovery of metals from electronic waste is of environmental and economic interest. The majority of these metals are typically located on printed circuit boards (PCBs) within electronic devices (Tuncuk, Stazi et al., 2012). Hydrometallurgical processes are considered a viable option for small scale metal recovery from waste PCBs, and generally involve the following steps: disassembly for removal of hazardous and reusable parts, size reduction, physical separation, successive leaching stages for metal dissolution and finally recovery of metals from leach solutions."

Jan 1, 2018

By B. K. Mohapatra

Small manganese ore bodies in south Odisha, India occurs both as stratiform and stratabound ore bodies. These two ore bodies show contrasting mineralogical, petrographical and chemical characteristics. Stratiform type of Mn-ores consists of manganese, iron and silicate- phases in approximately same proportion. In contrast, stratabound ore bodies contain a high proportion of manganese oxides, silicates and phosphorus phases. Phosphorus is found within apatite in the stratabound ore bodies while in the stratiform ore it occurs as an adsorbed state with iron phase (goethite). Both ore bodies are low-grade (17-23% Mn) therefore do not have a market value. However, the stratabound ores are enriched in phosphorus (P2O5: >1%) compared to the stratiform ores. Both the ore types were processed through gravity, magnetic and roast reduction followed by magnetic separation techniques. The strata bound ore could be upgraded to 33% Mn from a feed of 23% by combination of dry and wet magnetic separation methods. But the phosphorus content also suits up (P2O5: 1.2%) in the processed product making it unsuitable for further use. The stratiform ores do not respond to either gravity or magnetic separation because of close association of manganese with iron phases. However, this could be beneficiated through roast reduction followed by magnetic separation. An ore with 17% Mn content could be upgraded to 40% Mn with a 42% yield and 78% recovery. The goethite, having phosphorus, converts to magnetite and is retained within the magnetic fraction, thereby reducing the concentration of phosphorus in the non-magnetic fraction, which becomes the product. This report demonstrates the influence of ore petrology in determining the up-gradational potential of manganese ore in the southern Odisha, India. Keywords: manganese ore, physical beneficiation, phosphorus rich ore

Sep 1, 2012

By Willis Forsling, Prabhakar Swarna, Hanumantha Rao Kota

The solubility of wollastonite and its Hallimond flotation behavior as a function of dodecylamine concentration and pH are examined. The flotation response is characterized by adsorption and surface energy in the presence of amine. The methods of UV-Visible and FT-IR spectroscopy for adsorption and sessile-drop contact angle for surface energy estimation are employed. The results of wollastonite dissolution clearly showed its non uniform dissolution. The surfaces are depleted with calcium ions and became rich in silicon within 10 min of flotation time. Maximum flotation of wollastonite corresponds to a half monolayer coverage of amine, which is substantiated by the surface energy parameters. A good correlation between flotation, adsorption and surface energy as a function of amine concentration and pH was observed. The sudden increase in wollastonite flotation and amine adsorption at and above 5x10-5 M initial amine concentration is thought to be due to two-dimensional precipitation of amine on surface in accordance with the recent 2D-3D precipitation model of amine adsorption on silicate minerals.

Jan 1, 2003

By R. Sakthivel

Blue dust is a high grade soft haematite material containing 96.14% Fe2O3 transformed into magnetite (Fe3O4), when it is subjected to planetary ball milling in the presence of iron powder as reducing reagent. X-ray diffraction (XRD), Field emission scanning electron microscope (FESEM) and Laser particle size analyser have been employed to characterize various samples collected at various milling times to know the phase evolution, particle size distribution and morphology of particles. X-ray diffraction studies reveal the formation of magnetite phase at the optimum milling time of 40 hours. Vibrating sample magnetometry (VSM) study demonstrates, that sample obtained at 40 hours of milling time exhibits saturation magnetisation of 14.757 emu/g whereas the starting material used in this study shows only 1.0425 emu/g. Keywords: Blue dust, reaction milling, magnetite, saturation magnetization

Sep 1, 2012

By Robert van Hille, Alison Lewis

The precipitation of a selection of metals from both a synthetic and an actual metal-rich effluent was investigated. The experimental aspects of this study were carried out in a two-stage process consisting of a pre-treatment clarifier and a fluidised bed (pellet) reactor. Each unit operation in the two-stage process was investigated separately. The pre-treatment clarification stage at pH ˜ 5 resulted in a 99.9% removal of iron and 97.3% removal of aluminium. The pellet reactor was used to precipitate nickel as nickel carbonate from a pure stream and a removal efficiency of 99.6% was achieved. The high local supersaturation at the reagent inlet points caused the formation of a large amount of fines, but these agglomerated onto the pellets up the length of the bed. For copper precipitated as copper sulphide from a pure stream, a maximum removal efficiency of 92% was achieved. The high local supersaturation at the reagent inlets also caused the formation of a large amount of fines, but the extremely sparingly soluble nature of copper sulphide meant that the fines were not agglomerated up the length of the bed. For removal of cobalt as cobalt carbonate from an actual stream, a stable cobalt removal of only 60% was achieved. This was found to be due to the presence of magnesium, which reduced the cobalt precipitation efficiency through the formation of the magnesium bicarbonate ion.

Jan 1, 2003