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By S. K. Pan, M. P. Srivastava, N. Prasad

"Dalli mines of Bhilai Steel Plant, India is fully mechanized iron ore mine having wet processing system. It has a capacity to treat 5 Mt of ROM. In processing circuit of Dalli mines, scrubbing, wet screening and classification operation is being carried out. Average slime generation for the last five years is about 14% of ROM. As the mining has reached to the lower benches, fines generation is more. As a result, very fine and heavy particles, which settle fast, are being discarded with the slime to tailing pond. These heavy and faster settling particles were causing jamming in the thickeners.Laboratory investigations were carried out at Research and Development Centre for Iron and Steel (RDCIS) to suggest a suitable scheme to recover high quality fines so that the availability of thickener can improve. The slime samples were first treated in a floatex density separator. The concentrate obtained from the floatex density separator was treated in hydrocyclone. Laboratory investigations indicated that the slime with 49% Fe, 12.7% silica and 10.7% alumina can be upgraded to 62.1% Fe, 3.3% silica and 2% alumina with 36% material recovery. Based on the laboratory studies ,a system was installed at Dalli minesThe general arrangement of the system is shown in Fig. below."

Jan 1, 2003

By Z. Kwela, A. Manhique, W. W. Focke, W. van der Merwe

"The main features of the de Wet improved alkali fusion process for the manufacture of AZST are: Fewer process are steps necessary; radioactivity is removed by leaching rather than by precipitation; fewer waste streams are generated; there is less waste to discard and alkali reagent is recovered in the form of a sodium silicate solution that is essentially free of radioactivity.Here we report on our efforts maximize the alkali recovery in the sodium silicate product stream: Milled zircon, d50 ˜ 9 µm, was fused with caustic soda pearls in open reaction vessels at temperatures between 650°C and 850°C. Fusion times of 1, 2, 4, 24 and 336 hours (with intermittent milling) were investigated. The fusion products were characterized by infrared spectroscopy, X-ray diffraction and by wet chemical analysis.For prolonged fusion times the fusion products approached equilibrium compositions. However, the phases Na2ZrSiO5 and Na4Zr2Si3O12 observed at 850°C did not form at 650°C. Since these compounds do not hydrolyze in water they limit the recovery of alkali in the sodium silicate product stream. For 2-hour fusions a broad spectrum of non-equilibrium reaction-products, that are rich in sodium silicates, is formed."

Jan 1, 2003

By Jochen Petersen, David G. Dixon

"Although heap leaching may be perceived as a somewhat low-tech route for the extraction of low-grade minerals, the underlying physical, chemical and biological processes are in fact extremely complex. There has been increased interest in heap leaching of sulphide minerals in recent years with the advent of controlled bio-heap leaching, and the need to mine more marginal ore deposits.A detailed investigation into the dynamics of heap leach processes has provided much insight into the underlying complexities, and has led to the development of a sophisticated modelling tool. Some of the features include mineral kinetics, particle level effects, bacterial growth, oxidation and adsorption, gas adsorption, pore diffusion, bulk advection, gas balance and heat conservation.Two case studies are presented which illustrate specific features of the model for different applications and how these have helped to identify key areas of concern. In each case the model has proved as an invaluable tool either for the improvement of existing heap leach practice or for the development and assessment of novel applications."

Jan 1, 2003

By R. Batterham

"The history of mineral processing is indeed long and has always been tied to mining methods of the day. While many new processes and devices have been developed, the most significant trend in recent times has been the ever increasing scale of operations. There is serious doubt this ongoing trend is enough to match the global trend of falling grades and rising energy demands needed for mineral processing. As well we see that globally, the social licence to operate for mining (and hence mineral processing) is far from secure. Indeed, some argue that mining as we know it is dying and in the future, mining will be much more environmentally secure, even to the extent of insisting upon “in place” recovery and only bringing to the surface the valued product. In this paper we comment on the ramifications of broader uptake of more sustainable mining for mineral processing methods and address the specific question of whether recent progress in in place recovery will lead to a timely breakthrough. The answer proposed is that this is possible in the next 10 - 20 years but in the meantime, the focus is just as likely to be on removal of waste much earlier in circuits. Either way, mineral processing as we know it will change significantly. INTRODUCTION Mineral processing has a long history well covered in a recent publication (Habashi, 2006) who points out “the ancient Egyptians knew already that it would be easier to melt an earth rich in gold particles than another which is poor. As a result, all efforts were made to enrich the gold by washing away the light gangue minerals. Similarly, another ancient method for enriching gold particles from a river stream was by means of fleece, hence the Greek myth of the “golden fleece”. Since the middle ages, striving for improved economics has driven a string of innovative developments in milling and separation. The reader is again referred to the informative and illustrative text by Habashi."

Jan 1, 2018

By S. Swaroopa

Copper-chromium mixed oxides are widely used as catalyst for organic chemicals industry, NOx and CO oxidation, solid propellant etc. In the present investigation, one such spent Cu-Cr catalyst has been tested for recovering copper and chromium values through hydrometallurgical route. The spent catalyst used in this study contains about 42% Cu and 36% Cr. Phase analysis through XRD indicates that major phases are copper chromium oxide (CuCrO2) and copper chromate (CuCr2O4) while minor phase is copper oxide (Cu64O). SEM images show that high energy ball milling changes surface morphology significantly ? more regular shaped grains in unmilled samples changed to fine agglomerates. Surface area also changes significantly due to milling. Preliminary leaching experiments with NH3 and H2SO4 media using unmilled samples indicate that both the media are suitable for selective extraction of copper. About 55% copper recovery is achieved in 2 h using 1.2 M NH3 + 0.2M (NH4)2SO4 solution at 100°C. Increasing NH3 concentration or temperature does not improve the recovery significantly. Under the above conditions chromium, dissolution is insignificant (max. 2.24%). XRD analysis of the residue indicates that copper chromate fraction (CuCr2O4), which is a spinel structure, remains mostly intact. In sulphuric acid media at ambient temperature, 47% copper recovery is achieved with 7.5% (v/v) H2SO4 and maximum of 57% with the increase in acid concentration to 20%. However, 67% recovery is achieved by increasing the leaching temperature to 150°C. High energy ball milled samples show improved leaching efficiency. Under the leaching conditions of 7% H2SO4 (v/v), 2% pulp density, 80°C an unmilled sample yields 47% Cu recovery whereas 3h and 5h milled samples yield 65% and 90% Cu recovery respectively in 2h leaching time. Influence of temperature is also more pronounced in milled sample leaching in comparison to unmilled sample. Water leaching of alkali (NaOH) roasted milled sample carried out at 750°C for 2 h with 100% NaOH (w/w) resulted in 80% Cr recovery as compared to 37% Cr recovery using unmilled sample under the same conditions. Keywords: spent catalyst, copper, chromium, leaching, mechanical activation, roasting

Sep 1, 2012

By Herman Mendoza, Luisa Ciriaco

An investigation of the seeding mechanism using heterocoagulation and the Derjaguin - Landau - Verwey - Overbeek (DLVO) theory of two pure minerals is the objective of this study. The seed was silica with modal diameters of 4.529 µm (fine particles) and 5.216 µm (coarse particles) and the test powder was hematite with a modal diameter of 0.883 µm. Parameters included variations in the concentration and particle size of silica. Both particles were first subjected to size determination and settling tests via Stoke’s Law. The silica-hematite system was then suspended in 0.001 M KNO3 electrolyte solutions where pH was adjusted. Afterward, the suspension was agitated and was allowed to settle at different time intervals while obtaining turbidity readings. Results through settling time and turbidity vs. pH graphs indicate that maximum heterocoagulation occurs from pH 2 to 5 while minimum heterocoagulation occurs from pH 6 to 7. At these pH levels the zeta potentials of silica and hematite are negative and positive, respectively. On the contrary, repulsive forces dominate the system from pH 8 to 11 due to the particles’ negative zeta potentials. Furthermore, the attachment of hematite to silica increases when the parameters become larger thereby increasing the effectivity of heterocoagulation at acidic to neutral pH levels.

Jan 1, 2014

By Gülay Bulut, Ferihan Göktepe

Pyrite is the most abundant and widespread sulphide mineral and its flotation has been investigated by many researchers. It is well known that, pyrite is floatable under acidic conditions and recovery drops with increase in alkalinity due to changes in solubility of iron hydroxides on the pyrite surface. Most of the works also revealed out that pyrite displays variable behaviour in flotation circuits. This behaviour mainly related with origin and mineralogical composition of ore, liberation size, electrochemical behavior of minerals constituting ore, the trace and minor element content of the mineral, texture, application variables belonging to flotation circuits. In this study, copper activation effect was examined on different origin of pyrites. The experiments were performed with five high grade samples of pyrite from the different mining districts of Turkey. The pyrite samples were different from each other with respect to either their physical or chemical properties; they were different physical appearances and contained different associated minerals. In the micro-flotation tests, 1x10-4 mole/L copper sulphate and 1x10-4 potassium ethyl xanthate were used as flotation reagents. First of all pyrite samples were floated using only xanthate at different pH. Results showed that best floatation results obtained at acidic pH range for all pyrite samples. When copper ions were used to activate, all pyrite samples floated at neutral and basic pH values, too but depending on the samples, recovery and pH ranges were slightly changed.

Jan 1, 2014

By A. Lewis

"Thiol collectors including the xanthates and dithiophosphates have dominated the sulfide mineral processing industry for over a century. Tecflote represents completely different chemistry, without sulfur or phosphorus, and will float all sulfides and associated precious metals. As these collectors are surfactant in nature, they comprise a head group which binds to mineral surfaces, a spacer and a long hydrophobic tail. The modification of the spacer behind the head group allows for collector optimisation for different sulfide ore types and process conditions.The Tecflote surfactants have been designed to be either very selective against pyrite at the natural pH of the ore (pH 7-9) or to float all sulfides including pyrite. Depending on the ore type and the process flow sheet, the use of lime can be maintained, reduced or completely eliminated.Tecflote can be used either as a rougher collector giving good recovery and grade for the sulfide minerals or it can be used to target valuable minerals after regrind and through cleaner flotation. It has repeatedly shown to be very effective at holding onto gold through the cleaner steps. The low solubility has a significant impact on the mechanism and surface activity of the collector, resulting in a very different flotation response compared to conventional thiol collectors.INTRODUCTIONXanthate was first made in 1882 by Zeise and first used in flotation in 1924 (Keller, 2018). In 1946 Keller patented thionocarbamate as a collector, which was produced by Dow Chemicals (Keller, 2018). Later it was replaced by Dow product Z-200, while dialkylthionocarbamate was discovered by Harris et al. (Harris, 1954. No significant chemistry change to collectors has occurred since they were introduced in the mid-20th century and now that the feed grades have been declining over the last decades creating a need to find more selective collectors to extract difficult and complex ores and pushing the industry to look at other reagents."

Jan 1, 2018

By K. Saberyan

In this study, solvent extraction of zirconium by using triphenylphosphine oxide as extractant has been investigated. The results showed that extraction of zirconium by triphenylphosphine oxides in nitric acid and hydrochloric acid media were negligible. Extraction of zirconium in acetic acid media with concentration of 0.01~0.2 M has been studied and the results showed that the maximum percent of zirconium extraction was 40% in acid acetic with concentration of 0.01 M. By addition complexing agents such as potassium thiocyanate with the concentration of 0.01~0.2 M zirconium extraction increased up to 86% in 0.2 M potassium thiocyanate. By addition of sodium salicylate with concentration of 0.01 M and in pH=2.5, the maximum extraction of 96% was achieved. The striping of zirconium from organic phase can be carried out by 0.5 M solution of sulfuric acid.

Jan 1, 2014

By K. Price, G. Wang, L. R. Moore, Y. R. Xiong, J. Gu

"Sand is a naturally occurring granular material that is a result of the physical or chemical breakdown of rocks. Raw/natural sand contains various minerals, and it is this combination of minerals that brings the value to the construction aggregate industry. However, it is the quartz component of sand that is valued in its application as industrial silica in glass, high purity quartz, foundry sand, and oil and gas fracturing. Depending on the industry, the grade requirements can be the concentration of SiO2, particle size or shape, as well as contaminants such as the heavy refractory minerals, clays, fines, and alkali metals. With the ever declining mineral feed grade, processors continue to face challenges making the industry specific concentrate grade. As such, it becomes more important to tailor make the processing reagents to fit the mineral, processing conditions, and desired quality specification. This paper focuses on the application of novel collectors towards the beneficiation of sand for each of the major industrial silica applications. INTRODUCTIONQuartz is a mineral composed of a framework of silicon and oxygen atoms. It is the second most abundant mineral in the Earth’s continental crust. There are many species of quartz, which are defined by the particle size, shape, and color. Silica sand is one of those species, which is the byproduct of the physical or chemical breakdown of quartz containing rocks or crystals. Geologist define silica sand as a silica mineral with a particle size between 0.05 and 2 mm in diameter (Zdunczyk, 2001). Silica sand has significant value to society in recreation (beach sand and toy boxes), construction aggregate (concretes and asphalt), industry (iron & steel casting, fracturing proppants, and glass), as well as specialty products such as semiconductors or silicon wafers used in electronics.The aggregate business is the dominant consumer of silica sand products. Conversely, glass making, foundries (casting material), abrasives, and fracturing proppants are the dominant applications for industrial silica sand. Not much beneficiation is required for sand products going into the construction industry, other than sizing and scrubbing to remove clay. However, the industrial silica sand applications are dependent on particle size, shape, and degree of contaminants, which sets the market value (table 1). Therefore, as the more specialty products are produced, more sophisticated techniques and chemistry need to be applied to ensure the appropriate quality is met."

Jan 1, 2018

By Chuansheng Luo, Qiuyang Hong, Lili Zhang, Dongyun Liang

"The metallogenic rock of a sandstone-type Cu ore is arkose-quartzite as well as siltstone and the cement is composed of argillaceous minerals including sericite, chlorite, etc. and carbonate minerals including calcite, dolomite, etc. A detailed process mineralogy study on this complex copper ore was carried out using MLA combined with traditional research methods. According to the results, there are many types of Cu minerals including copper sulfideminerals, secondary copper sulfideminerals, copper oxideminerals, copper carbonate hydroxide minerals and copper silicate minerals in the ore. Based on the occurrence of Cu, the copper existing as copper sulfide minerals (bornite, chalcopyrite and chalcocite) and copper oxide mineral (malachite) which have a good floatability accounts for 49.28% while the copper (chrysocolla) hard to be recovered by flotation and the copper existing in the cement (sericite, chlorite, psilomelane and limonite) accounts for 48.65%, and the copper existing in the carbonate minerals (calcite and dolomite) accounts for 1.72%. The process mineralogy study indicates that the process "beneficiation combined with hydrometallurgy" should be applied due to the various occurrence of Cu. The abundance of calcite and dolomite is about 12%, so removing these acid-consuming minerals by floatation is an effective way to reduce the acid consumption in the hydrometallurgical process and the lowest Cu loss is 1.72%. So the process "floating copper minerals-floating calcium minerals (calcite and dolomite)-leaching copper from the tailings" is used in the pilot tests. The recovery of floating copper and leaching copper from tailings is 46% and 30% respectively, so the total recovery of copper is 76%. Compared with the original process "leaching copper from crude ore-floating copper from the residue", the total recovery reduces by 1% but the acid consumption of producing per ton of copper decreases from 37t to 12t. The new technology process has a great advantage."

Jan 1, 2014

By Bertil I. Pålsson

The most common REE containing mineral that is worked today is bastnäsite. It means that mineral processes are adapted to it and that the metallurgical separation techniques for winning of individual REE are adapted to bastnäsite concentrates. For all other deposit types, suitable mineral processing methods and separation technologies need to be adapted and/or developed. Preliminary mineralogical analyses indicate that slightly less than half of the REE in the tailings dumps at LKAB/Kiruna are associated to apatite. The rest is in the minerals monazite (maybe associated to apatite) and allanite. At least allanite is probably not floatable with reagents commonly used for apatite. Mass and element distributions for the tailings sand reveal that very little apatite is present above 300 µm, and that approx. 30 % is below 20 µm. REE does not follow P2O5 completely and are also present in coarser fractions. Flotation results show that the best condition for both apatite and REE winning is pH 9, high collector addition and low dosage of water glass. Under these conditions, the lab-scale flotation gives an apatite concentrate with at least 30 % P2O5 at 70 % recovery. REE follows apatite in the cleaner steps but only partly. Its recovery is approx. half compared with apatite. The reason for the low REE recovery is likely to be that REE to a large extent is trapped in non-winnable minerals, especially allanite. The REE grades in the concentrate are expected to be in the range 3000 ? 4500 g/ton. Keywords: flotation, REE, apatite, monazite, allanite

Sep 1, 2012

By V. K. Kuppusamy, M. Holuszko

"Lamps and lighting products are the most commonly used electrical products around the globe. With the improvement in lamp technologies, lighting products have grown complex and hence require an improved recycling process. The LED lamps consist of various valuable metals such as iron, copper, aluminum, chromium, silver, and gold, as well as non-metals such as glass, plastics, and fibers. In addition, there are also traces of hazardous substances such as lead, arsenic, and mercury. A major step in the recovery process is size reduction, and researchers have suggested that up to 40% of the total valuable material is lost during the shredding and grinding processes. SELFRAG is a high voltage selective fragmentation comminution technology that uses high voltage pulses in a water medium to efficiently separate the metals at a coarser size without generating many fine particles. It has been proposed that during the fragmentation process of electronic waste (e-waste), the metals can be separated without fine grinding. This research considers the applicability of high voltage pulse fragmentation for LED lamps. Eight different types of LED lamps were processed through the SELFRAG unit at varying pulses to study metal liberation. The product obtained was characterized for metal liberation, metal grades, and liberation analysis. The specific energy consumption for this size reduction process was also monitored. INTRODUCTION Lamps and bulbs are the most commonly used electrical products in homes, offices, industrial operations, and streets. According to Energy Star research (2006), an average US household has more than 40 sockets for light bulbs and consumes approximately 2100kWh every year for lighting. The development in lamp technology has pushed the boundary for newer products. The LED lamps have been taking over the market from the incandescent bulbs and compact fluorescent lamps (CFL). According to the US Department of Energy (2012) and myLEDlight.com (2007), LED lamps have several benefits over other lamps. LEDs produce light hemi-spherically, which increases their efficiency in directional light emission. It has higher breakage resistance from vibration or transportation. LED lamps use up to 90% less power than incandescent bulbs thus making them highly energy efficient; They have a longer lifespan, lasting 10 times longer than a CFL and 133 times longer than the traditional incandescent bulb. Because of all the benefits, Smallwood (2014) suggested that the market of LED lamps will grow to $12.2 billion by 2018."

Jan 1, 2018

By Ye Junjian

The feed ore is the concentrate of low intensity magnetic separation of pyrite tailings, containing TFe47.47%, S19.41% and SiOpyrrhotite. The exploratory tests showed that using a process of flotation followed by magnetic separation could respectively obtain a sulphur concentrate of S 31.08% with a recovery of 82.89%, and an iron concentrate of TFe 59.97% and S 9.52%with a recovery of 30.93%. The reason of iron concentrates with high sulphur grade was that the sulphur grade of flotation tailings was 7.03%. So enhanced flotation for pyrrhotite was investigated in this research. Results show that when the natural pH of ore pulp varied from 5.5 to 6.0, a reagent combination of FS, LH, and BJ displayed the optimum flotation performance for pyrrhotite. After comparisons made on different flotation processing, the previous flotation flow of ?one roughing, one cleaning, one scavenging system and middling reprocessing?, was found, among others, to have the best flotation effect, as the grade and recovery of sulphur concentrate were 31.08% and 82.89%, respectively, and sulphur content of the flotation tailings was 7.03%. The above results indicated it was difficult to raise further the effect of flotation desulphurization. The authors therefore suggested that oxidizing roast should be adopted following the magnetic process for the purpose of further desulphurization. Besides, flue gas containing SO2 8.25%. And the valuable minerals are magnetite and 2 generated from roasting could be reused for sulphuric acid production. Keywords: pyrrhotite, enhanced flotation, desulphurization

Sep 1, 2012

By Tom Leistner, Urs A. Peuker, Martin Rudolph

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

Jan 1, 2014

By Vladimir Vigdergauz, Sergey Kondratiev

The paper reviews the existing criteria of the formation of particle-bubble aggregates during flotation. It is shown that predictions obtained by these criteria do not completely fit to the interaction between mineral particles and air bubbles. Experimental results of the studies into the influence exerted by molecular forms of collectors on the particle-bubble interaction are reported. Rate of dry spot expansion on the surface of pyrite with various combinations of chemically and physically adsorbed xanthate are examined. It is shown that molecular forms of collectors accelerate the rate of dry spot expansion on the mineral surface after the local rupture of the water film between particle and air bubble. The authors come to a conclusion that the molecular forms of collectors remove water from the interlayer between mineral particle and air bubble during their contact. Similarities of the proposed mechanism with the action of ion-molecular associates of fatty acids and amines are discussed. Reagents with high surface pressure and rate of spreading at the water-bubble interface are required for the effective interfacial dewatering. It is concluded that the value of surface pressure can serve as the criterion for efficiency of physically adsorbed reagents. The low surface pressure indicates weak collecting ability but high selectivity of the collector. Therefore, the presence of the molecular forms of collectors in the sorption layer is the necessary condition for formation of particle-bubble aggregates, and comparison of the surface tensions of collectors could be recommended as the estimation criterion of their flotation activity and selectivity.

Jan 1, 2014

By M. M. Bugarin, P. J. van Staden, V. T. Conic, S. S. Dragulovic, R. M. Kovacevic, D. B. Milanovic

"The mineralogical and physico-chemical characteristics of a polymetallic sample from a mine of West Serbia suggest that it can be classified as a SEDEX type of ore. Those ores contain multiple value components, being inter-dispersed as fine grained aggregates. This prevents concentration by gravity or flotation concentration processes. Mineralogically, the valuable metals (Cu;Zn;Pb;Au and Ag) occur as pyrite, sphalerite, galena, tetrahedrite, chalcopyrite, covellite, arsenopyrite, and non-metallic minerals (barite, and waste minerals). Novel technologies are under development within this project for the recovery of all valuable metals from this very complex material. The work comprises the further treatment of solid residue obtained after Cu and Zn extraction by bioleaching, for the subsequent recovery of Pb and the precious metals Ag and Au. The residue is first treated with a saturated sodium chloride solution, whereupon a chloride solution of lead (NaPbCl3) is obtained. From the chloride solution, lead was deposited in the form of lead carbonate, followed by reductive melting, whereupon lead anode was obtained. Electrolytic refining of the lead anode, using a solution of PbCO3 in methane sulphonic acid (MSA-Methanesulfonic acid, min 99.5% CH4O3S, density 1.48 kg/dm3, Manufacturer: Carl Roth) as an electrolyte, yielded refined lead cathode. It should be noted that, after precipitation and separation of lead carbonate, the sodium chloride solution is restored to its original composition by the addition of make-up reagents and returned for another lead-sulfate leaching cycle. The solid residue obtained after leaching lead-sulphate, is leached in thiosulphate solution, with the addition of an activator, a catalyst and lixiviant for gold, to yield a thiosulphate solution of gold and silver. Since the content of gold and silver in solution is low (below 1 mg/dm3), they are first electrolytically concentrated on steel cathode and then refined to pure metals using well-known chemical methods. Note that, after the electrolytic separation of gold and silver, thiosulphate solution is recycled to the leaching step."

Jan 1, 2018

By André Mans, Frans B. Waanders

"Ferrosilicon (Fe-Si) is an important commercial material and it forms the basis of the powder used in dense medium separation (DMS) of various minerals in a minerals beneficiation process. Current losses of Ferrosilicon (Fe-Si), which is used in the dense medium separation (DMS) of iron ore at Kumba Resources, Sishen, South Africa occur due to adhesion to the separation products and also by being present in the effluent stream, due to abrasion. The losses contribute greatly to the running cost of the plant and the purpose of this project was to determine the characteristics of the unused Fe-Si and then to characterise the changes that occur during storage and the use thereof.A Scanning Electron Microscope (SEM) and Mössbauer Spectroscopy (MS) were used to investigate the characteristics of the fresh and used Fe-Si. The SEM analyses of the Fe-Si yielded a composition of 15 wt.% Si and 85 wt.% Fe with minor impurities of Mn and Cr (<1 wt. %), resulting in an ordered phase with a calculated composition of Fe2Si. The average density of the Fe-Si was found to be 7.177 g.cm-3 whilst the size distribution was determined with the d50 of the particles being approximately 30 µm. A slurry, containing 10% solids was prepared, which had a density of about 1.1 g.cm-3 and this slurry was used to conduct the various experiments under laboratory conditions at the university. Samples were taken at regular intervals from a storage container containing a lime solution as well as from a closed circulation circuit system, kept at a constant temperature of about 60°C. Mössbauer Spectroscopy yielded, for the new fresh Fe-Si-samples, a two-sextet spectrum with hyperfine magnetic field strengths of 19.9T and 30.7T respectively, and the yellow-brown froth was found to be akaganeite or ß-FeOOH.It was found that the biggest loss of Fe-Si was due to the abrasion of the particles during the DMS process. A possible change in magnetic properties was also observed, leading to further losses that could occur during prolonged use of the medium. No clear changes to the Fe-Si occurred during correct storage methods, as was initially thought."

Jan 1, 2003

By Minna Päällysaho

For the first time, the idea of sustainable development was recognised at a high political level at the UN Conference on Environment and Development held in Rio de Janeiro in 1992 (UNEP, 1992). Then the governments of the world committed themselves to promote sustainable development in their national activities and international co-operation. In 2001, the European Council approved the EU Strategy for Sustainable Development (European commission, 2011). This complements and supports the EU?s so-called Lisbon Strategy (European council, 2000) on competitiveness. The revised Strategy for Sustainable Development was approved in June 2006. Recently sustainability has had an important role in policy and decision-making while the public awareness towards limits of the environment has been rising. However, the indicators of industrial sustainability satisfy primarily the needs of corporate management and global investors. The information is often broad and non-specific and might occasionally even give a false impression. Moreover, contradictions between environmental, economical and social aspects also point out the unreliability of existing sustainability indexes. Therefore, the current state of affairs serves the interests of neither the industry nor the policy makers. Current corporate sustainability indexes and indicator systems need to be assessed with scientific methods encompassing the identification of their strengths and weaknesses. This requires quantitative and qualitative assessment and synthesis of existing indexes and indicator systems, providing new data on the functionality of existing corporate sustainability indicators. Therefore, the assessment lays the foundation for the development of new, more balanced sustainability index. Our first aim in this multidisciplinary article is to analyse existing global sustainability indexes for process industry. Second, we will introduce a first version of a new sustainability index for process industry, which includes the environmental, social and economic impacts of the plant, as well as legislation aspects.

Sep 1, 2012

By Li Maolin, Cui Rui, Wang Guanghui

"As the stirrer speed directly affects the motion of grinding media, and hence the interactions with material particles to be ground, the rotation speed of a stirred mill is well recognized as one of the most important factors affecting the grinding performance. In this work, the effect of stirrer speed on grinding performance in terms of grinding rate and grinding energy efficiency was quantitatively investigated. Batch wet grinding tests of quartz powder at different stirrer speeds were performed, using a self-made horizontal stirred mill with alumina balls as grinding media. Grinding time, operating power and the sizes of ground product were recorded to analyse the grinding performance. The test results showed that grinding processes followed the first order grinding kinetics. The grinding rate constant increased with the increasing stirrer speed. Based on the grinding kinetics, the grinding energy equation was established. The energy utilization coefficient in the energy equation can be used as an indicator of energy efficiency. The energy efficiency decreased with the increasing stirrer speed. Quantitatively, with the stirrer tip speed increasing from 4.25m/s to 9.35m/s, the grinding rate constant was improved by 441.47%, whereas the energy utilization coefficient was decreased by 39.35%. The grinding rate constant and energy utilization coefficient can be used to evaluate the grinding performance when the grinding conditions need to be adjusted. The adjustment of grinding conditons would be optimal when grinding rate get significant improved with little decrease of energy efficiency."

Jan 1, 2014