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By R. Van Hille, A. E. 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 pretreatment 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 hydroxy-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 (See Figure 1).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. In Figure 2, the global supersaturation ratio was relatively low, and thus there is little homogeneous nucleation and degree of fines formation. However, the fines occurring after the third sulphide input point (at 30cm from the bottom of the bed) indicate that local supersaturation also plays a critical role in fines formation. It was therefore concluded that, for the copper sulphide case, it is essential to control the supersaturation at the inlet points in order to prevent fines formation altogether, as it is not possible to agglomerate the fines once they exist in the bed."

Jan 1, 2003

By R. Van Hille, S. Lacour, A. E. Lewis, K. Peterson

"This paper compares thermodynamic modelling results with those obtained for copper sulphide removal from aqueous solution in both continuous and batch experiments at laboratory scale. Sulphide precipitation has been demonstrated to be an effective method for heavy metal removal. The advantages are the high degree of metal removal at low pH, low quantities of sludge formation, the ease of de-watering and low reactor retention time due to high reactivity of sulphides. However, the low solubility of sulphide species can lead to spontaneous nucleation of fines, which are difficult to remove.Theoretical modelling was carried out using ASPEN Plus™ and OLI systems Inc ESP process. Both simulators were used to calculate copper sulphide recovery and residual aqueous copper concentrations as a function of pH. The predictions were then compared with experimental results. Both simulations predicted that all of the inlet copper would precipitate as sulphide CuS(s) over the entire range of pH and sulphide: copper molar ratios investigated. The simulation results were strongly influenced by the number of chemical species and the nature of the thermodynamic data taken into account in the model.The continuous experimental studies were carried out in a fluidised bed reactor (FBR). Copper sulphate was reacted with sodium sulphide and the solid precipitated directly onto the pellets in the FBR. The use of sulphide was motivated by high sulphate levels in local acid mine drainage and the ultimate integration of the metal removal process with a biological sulphate reducing process that produces an aqueous sulphide stream.A maximum dissolved copper removal of 99.6% (AAS analysis) and a total removal efficiency of 95.8% (dissolved copper minus fines) were achieved. Stoichiometry of the precipitate was determined from SEM/EDAX analysis (atomic percentages) and was close to 1/1, irrespective of the operating conditions."

Jan 1, 2003

By Glasswell K. Nkonde, Fredrick Chileshe, Steven Simukanga

Improving food security by increasing crop output is a primary objective for most countries in the sub- Saharan region. Most soils in the region are deficient in phosphorus an important nutrient after nitrogen in plant growth. Phosphates are therefore used together with nitrogen and potassium based fertilizers in improving crop production. Zambia like many other countries in the sub-Saharan region imports phosphate fertilizers for use by its farmers. However, indigenous phosphate deposits of igneous origin exist in Zambia of which the main ones are Chilembwe in Petauke district, Mumbwa sugarloaf in Mumbwa district, and Nkombwa Hill in Isoka district. If commercially exploited, these deposits could become a ready source of inexpensive phosphate for the local farming communities in the country. Previous research has shown that partially acidulated phosphate rock (PAPR) produced using Chilembwe phosphate rock is just as agronomically effective as the imported superphosphate fertilizers on food crops in most of the Zambian soils. PAPR is produced by reacting finely ground phosphate rock with only a fraction (usually 50%) of the stoichiometric quantity of the sulphuric acid required to fully convert the apatite in the rock to monocalcium phosphate thus making the process cheaper in terms of acid consumption than the poduction of single superphosphate where the apatite in the rock has to be fully converted to monocalcium phophate. The factors that affect the percentage of available P2O5 in the PAPR produced include particle size of phosphate rock, degree of acidulation, concentration of acid, process temperature profile, residence time and drying temperature. These factors were studied in a 25kg/hr PAPR pilot-plant in the School of Mines at the University of Zambia using Chilembwe phosphate rock. The PAPR pilot-plant consisted of a rotary drum granulator as the main reactor, a rotary drum dryer and a triple deck vibrating screen. Ground phosphate rock was reacted with sulphuric acid and water in the granulator to form a granular product which entered the drier. The dry product was screened into three size fractions. The 1 – 4 mm size fraction was the final product whilst the –1mm size fraction was recycled. The +4mm size fraction was sent to a crusher while the crushed PAPR was sent back to the screens.

Jan 1, 2003

By O. N. Mohanty, S. Mohan Rao, N. D. Rao, T. Mukherjee, P. V. T. Rao

"Chromite ore is an indispensable raw material in the manufacture of ferro-chrome and charge-chrome, which are used for the production of stainless and other alloy steels. The demand for chromite ore is ever increasing because of increasing consumption of these steels. Keeping this in view, Tata Steel is keen to recover values from fines and wastes, and also to produce value added products from their captive chromite mines and its processing plants.Tata Steel has its captive chromite resources at Sukinda, Orissa. They contain two ore types, i.e. (i) Ferruginous and (ii) Siliceous. The generation of off-grade ores is an increasing trend and simultaneously customer quality requirements are becoming ever more stringent. The ferruginous type ore also contains a considerable quantity of in-situ fines (~20% particles below 0.5 mm) that compound the beneficiation problem.In many places, in India and abroad, mined non-marketable off-grade and low grade chromite ores are upgraded by using either simple classification techniques like screw classification, hydrosizing, hydrocycloning or conventional gravity concentration processes such as Heavy media separation, Jigging, Spiraling, Tabling etc.At Tata Steel, the ferruginous type ores are treated in Chrome Ore Beneficiation (COB) Plant that comprises: a crushing and grinding circuit; a classification circuit using hydrocyclones; and a beneficiation circuit using 4 stage spirals in the coarse circuit (-0.5+0.1 mm) and 3 stage spirals & tables in the fine circuit (-0.1+0.038 mm). In this process, 3 types of tailings are being generated and together analyses about 17 % Cr2O3, which is high. From the present operation the chromite recovery is around 70% and could not produce coarse concentrates (+0.5 mm size). Whereas the siliceous type ore is treated in the Lumpy Ore Processing (LOP) plant, consisting of crushing-washing & classification-hand sorting operations, to produce marketable grade lumpy ore and –10 mm de-slimed fines. These fines are intermittently treated in the COB plant. The higher silica content (greater than 1%) and low Cr/Fe ratio (less than 2.8) are the problems with these concentrates."

Jan 1, 2003

By Saveliy F. Kaplan, Valeriy N. Tsyplakov, Vasily N. Kovalev, Igor A. Agapov, Nikolai V. Vorob’ev-Desyatovskii

"Based on the experiments, a possibility of successful processing of double-refractory gold sulphide concentrates with a high content of natural organic carbon, which has a high sorption capacity toward gold chloride complexes, has been demonstrated. The proposed approach involves deep burnout of sorption-active organic carbon in an autoclave at a higher temperature and a longer retention time. INTRODUCTION It is known that one of the reasons why gold-bearing ores and concentrates are refractory is the occurrence of fine gold in sulphides (usually in pyrite and arsenopyrite) in ores and concentrates. In addition, refractory gold-bearing ores and concentrates also contain an organic carbonaceous material, which has a sorption capacity towards gold chloride complex, making the ore or concentrate even more refractory. In pressure oxidation, metallic gold is oxidized by Fe (III) aqua-ions and complex Au(Cl)4- ions are formed at temperatures over 180°C, in the presence of chlorides contained in ores. Complex gold anion is adsorbed on the organic carbon surface and then reduced to Au0; the chloride ion is regenerated and gold, adsorbed on organic carbon microparticles, is ultimately transferred to tailings (preg-robbing). Currently, there are several suggestions how to suppress preg-robbing (Simmons, 1998, Pyke, 1999, Rees, van Deventer, 2000, Zhao Jun-wei, 2008). It can be done by reducing the organic carbon content by processing (flotation, etc.),reducing chloride ion concentration by preliminary washing of concentrates in thickeners, reducing the adsorption capacity of organic carbonaceous material by introducing some organic substances that are strongly adsorbed on its surface (blanking agents), and reducing the redox potential of the slurry liquids by introducing neutralizing agents (limestone)."

Jan 1, 2018

By Hideki Yamamoto, Norihiro Murayama, Junji Shibata

"Hydrothermal syntheses of zeolite from coal fly ash were carried out by using various alkali sources. NaOH, Na2CO3, KOH, K2CO3 and their mixture were applied for an alkali source of zeolite synthesis. The various physical properties of the reaction product, such as the kind of zeolite crystal, cation exchange property, surface texture and so on, was investigated through the zeolitization reaction from fly ash. The mechanism of zeolitization reaction was considered from these results.Zeolite P(NaP), hydroxysodalite(HS) and chabazite(K-CHA) are synthesized as zeolite species, when fly ash hydrothermally reacts in various alkali solutions at 393K. The crystal structure of the products obtained in NaOH solutions for 3h changes from NaP to HS with increasing NaOH concentration. K-CHA formation in KOH solutions needs 10h of reaction time, which is longer than that of NaP or HS.Dissolution, condensation and crystallization steps exist in the zeolitization reaction from fly ash, and the particle surface of products remarkably changes in each step. The fly ash is spherical particles and the surface is smooth(Fig.1(a)). The dissolution of fly ash occurs in the heating process until 393K, and the particle surface changes like unevenness(Fig.1(b)). In case of NaP, the condensation of aluminosilicate ions takes place at 373-393K, and the amorphous aluminosilicate is deposit on the unreacted fly ash(Fig.1(c)). The crystallization of NaP already begins to occur at 393K and the surface is covered with fine zeolite crystals for 24h(Fig.1(d))."

Jan 1, 2003

By Sebastian Fredes, Williams Calderon, Mauricio Toledo, Gonzalo Montes-Atenas

The influence of the temperature on leaching kinetics of copper-bearing minerals has been widely acknowledged: the leaching of copper oxide ores is generally described as exothermic reactions while copper sulfide ores are associated with endothermic reactions. Reports studying the influence of temperature on leaching kinetics at laboratory scale frequently involve the implementation of either fully flooded isothermal systems or jacketed column setups. Nevertheless, at industrial scale controlling or monitoring the temperature or temperature changes is almost impractical. In fact, leaching process is usually a large tonnage operation and changing the temperature of vast amounts of material would require an enormous amount of energy and highly specific heat transfer equipment. Preliminary computations on the amount of energy required to increase the temperature of a heap or dump in 1°C indicates that it would be impossible to find an energy source able to accomplish the task. In order to provide a solution to this matter it is suggested to create an energy managing protocol (EMP) that permits heat up or down the porous body locally taking advantage from the temperature gradients and from the reactivity of different regions within the material as a function of the leaching cycles. The aim of this study is to evaluate different heat transfer regimes in a 1 ton pilot column leach operation. It was found that best results of copper recovery are obtained when heating up the column in horizontal bands starting from the top of the column moving downwards as the leach cycle evolves. The system is expected to be suitable for industrial applications, but further development of the technique is required, particularly in the design of the heat transfer dispositive.

Jan 1, 2014

By Igor P. Solozhenkin, Peter M. Solozhenkin, Sanda Krausz

"In this work, authors will show the efficiency of computer technology and chemical programs at studying collectors for flotation of minerals of elements of platinum group (EPG). Clusters various minerals EPG (flotation reagents) are created, named us clusters minerals (reagents) as their structure corresponds to the chemical formula, and the distance between separate atoms corresponds to the known tabulated data. By molecular modeling are investigated clusters sperrylite PtAs2, stumpfilyte PtSb, sadberryte PdSb, sobolevskite PdBi, palladoarsenyte Pd2As, paolovyte Pd2Sn, rustenburgyte (Pt3Sn, Pt6Sn2) and their computer parameters (absolute rigidity, electronegativity, transfer factors of carry, charges of the atoms) are determined. Tellurides of palladium (IV, II) merenskyite PdTl2 and kotulskyte PdTe and platinum clusters are investigated: PtFe4, Pt3Fe, PtFe (Pt2Fe2), Pt2Fe (Cu) Ni. The technique of attachment of the collector (composites) to cluster atoms EPG is offered. For the first time, it is established that at linkage of flotation collectors on monodentate, bidentate and bridged to circuits with atoms clusters the minerals containing atoms As, Sb, Bi, Pb, Sn, reaction of connection with change of a degree of oxidation of these atoms and occurrence of a proton operates. It is executed virtual skirling organic compounds connections by the developed criteria from accessible libraries of a database. The principle of an estimation of interaction energy for flotation reagents with mineral clusters is offered. It is developed the prognosis of collector activity evaluation (P?AE) and his values for candidates in collectors for flotation of minerals EPG are calculated. For flotation of ores containing Pt and Pd minerals, a number of reagents, including compounds on basis P (III), for innovational technology of Pt, Pd mineral flotation are recommended. Key words: flotation, minerals, flotation reagents on the basis of phosphorus (III), molecular modelling, chemical programs, program ????? , electronic energy."

Jan 1, 2014

By Glaser. C., J. Balz, F. Logsch, R. Heiduschke, M. Leiker, P. Ay

The treatment of iron-hydroxide-containing water from ground water and surface water is achieved by a combination of the process steps of flocculation and subsequent mechanical dewatering. The aim is to create solid pellet structures by extending the structure forming flocculation process with a build-up pelletizing process which can be transferred directly into a drying unit. A Taylor-Couette-reactor (diameter of the inner cylinder – 40 mm, gap width – 5 mm) was used for these experimental studies. To produce the necessary flow profile the inner cylinder was rotated at a speed of 230 rpm. The iron hydroxide-containing suspension (dry matter content: 2 mass %) was added simultaneously with the addition of a cationic high-molecular flocculant in various flocculant dosages and residence times of 5 to 15 min. The pellets were examined for parameters such as geometric dimensions, dry substance content and dewatering behaviour. As the results show, there is a direct relationship between the residence time and the geometric dimensions of the pellets. After a residence time of 5 min, round pellets with an average diameter of 6 mm were formed. With an increase in the residence time up to 15 min, a compaction of the pellets could be observed, which resulted in an increase in the dry substance content of 8.0 to 11.2 mass % on average. After completion of the pelletizing process, the pellets were mechanically dewatered by filtration. By applying this innovative wet pelletizing of iron-hydroxide containing suspensions in a Taylor-Couette-reactor, it is possible to carry out the process of flocculation combined with the pellet formation with simultaneous pellet compaction in a single process step. The resulting pellet structures are distinguished from conventional floc structures by an improved water discharge capacity. After classification the pellets can be marked directly as easy-to-handle bulk material, suitable as feedstock in percolation columns for the purification of contaminated fluid streams

Jan 1, 2018

By J. Shibata

The behavior in electric field of fine particles present in aqueous solution was measured in order to apply to the classification of fine particles. The sample particles used are spherical polystyrene particles with the average diameter of 0.03 µm, 0.1 µm, 1.0 µm, 4.3 µm and 9.6 µm. Electrophoretic mobility and zeta potential of various particles are measured by an instrument based on the principle of the laser Doppler effect. The influence of temperature, electrolyte concentration on the electro-phoretic mobility was investigated for various polystyrene particles. The electrophoretic mobility increases with increasing pH and temperature of suspensions. The measured electrophoretic mobilities are different from electrolyte concentration and particle size. The electrophoretic retardation effect and relaxation effect are considered to explain the behavior of fine particles in electric field by applying the electro kinetic theory of Wiersema et al. For all particle size, the electrophoretic mobility decreases rapidly in high concentration of KNO3 such as 0.1 mol/dm3due to the compression of electric double layer The forces acting the particles in electric field are considered to be electrical force, friction force and some other forces like relaxation effect and electrophoretic retardation effect which appear in ionic behavior. It is considered that the particle moving velocity depends on the particle size. When the particle size is less than 1µm, the velocity increases with increasing the particle size. On the oth-er hand, the velocity deceases with increasing in particle size, when the particle size is larger than 1µm. This phenomenon is considered to be interesting from the viewpoint of classification for fine particles. We found that the electrophoretic mobility of 1.0µm particles is larger than that of 0.1µm particles, and that it is possible to classify fine particles by using the difference of electrophoretic mobility by many experimental results. The phenomena can be explained by the forces acting the fine particles in the electric field. We can apply the behavior to classification of fine particles.

Jan 1, 2014

By Ana C. C. Pacheco, Maurício L. Torem

"The aim of this work was the study of the effect of the type (Fe3+, Al3+ and Fe3+ and Al3+ mixture) and of the coprecipitant concentration on As5+ removal by ACF. Removal of As5+ using sodium dodecyl sulfate (SDS) as a collector was studied by Adsorbing Colloid Flotation (ACF) at laboratory scale. The morphology of the precipitate retained in the foam was analyzed by Scanning Electron Microscopy (SEM/EDS).In order to investigate the effect of the initial concentration of Fe3+ on As removal, sets of experiments were performed with a concentration of Fe3+ in the proper range of pH (5,0 – 6,0) previously observed in the coprecipitation tests. As removal improves significantly as the concentration of the coprecipitant agent increases from 60 mg.L-1 (77,4%) to 80 mg.L-1 (99,7%). This is probably due to the higher concentration of ferric hydroxide (Fe(OH)3) which provides a larger surface area available for adsorption of As. From the initial coprecipitant concentration of 80 mg.L-1, As removal has shown to be rather high (? 99,7%), with the maximum being (99,9%) by using a Fe3+ concentration of 160 mg.L-1. Therefore, for a maximum As removal, under these test conditions, the optimum concentration of Fe3+ is 160mg.L-1.This paper also shows the effect of the initial concentration of Al3+ on As removal at a suitable range of pH (7,0 – 8,0). A very significant increase on As removal was found to occur as the initial concentration of coprecipitant was increased from 60 mg.L-1 (35,7%) to 80 mg.L-1 (97,7%) and a decrease in As floatability (43,7% - 54,5%) was found to occur from that Al3+ concentration amount. Based upon those results, the optimum Al3+ concentration so as to remove As under these test conditions is 80 mg.L-1."

Jan 1, 2003

By Andrew D. McCallum, Russell A. Heins

"Until the advent of intensive cyanidation, gold gravity concentrates were generally treated by tabling. The table concentrates were smelted while table middlings and tailings were recycled to the milling circuit for further grinding and subsequent leaching in the CIP/CIL circuit. Gold recovery on production tables is relatively low, often only 30 percent, and rarely above 60 percent. Significant factors in tabling performance are; mineralogy and the operator’s experience and ability. Units have been developed by Gekko Systems to treat both batch and continuous gold concentrates. Unit sizes are determined by leach kinetics and the required residence time of the concentrate in the unit.Gekko commenced the commercialisation of intensive leaching of gravity gold concentrates in 1997 with the first commercial prototype of the InLine Leach Reactor (ILR). Over 20 units are now installed worldwide with half that number on the African continent. South African mines, South Deeps (Placer Dome WAJV) and Target (AvGold) have both installed InLine Leach Reactors. Ashanti Goldfields have placed the ILR on their standard equipment list and have six operating units with a seventh on order. AngloGold installed one of the first ILR production units at Morila in Mali.Gekko Systems successfully installed an ILR1000 Batch unit at the Antapite Mine in Peru in December 2002. The unit was installed to treat gravity concentrates and to replace a shaking table. Following installation, gravity gold recovery increased from 15% to 40% of total gold. The unit was operational from start up and the first gravity batch treated achieved 98% gold recovery. The gravity concentrates also have a high silver content and 95% recoveries on silver were also achieved.Preliminary testwork identified that the concentrates required additional oxygen to achieve peak performance. As a result of optimisation work in the laboratory, leach kinetics in the ILR have been excellent with only 6 hours residence required to achieve maximum gold extraction."

Jan 1, 2003

By Brian Hart, Stamen Dimov

"In refractory ores, a substantial part of the gold content may be present as a sub-microscopic component within the mineral matrix of the various carriers. This type of gold may be present as finely disseminated colloidal size gold particles (<0.5µm) or as a solid solution within the sulphide mineral matrix. Such ores are not amenable to gold recovery by direct cyanidation. In order to liberate the sub-microscopic gold, the ore has to be oxidized before being subjected to gold cyanidation and extraction. Autoclave pressure oxidation (AC POX) of the sulphide ore and subsequent cyanidation is a common technology used to liberate the gold in such refractory ores. The additional presence of active carbonaceous matter in such ores (double refractory ores) represents another major obstacle for efficient gold recovery during the process of pressure oxidation and cyanidation. This carbonaceous matter (c-matter) can adversely affect the gold recovery due to its ability to adsorb, or pre-grob gold from the cyanide solution. Advanced micro-beam analytical techniques such as Dynamic Secondary Ion Mass Spectrometry (D-SIMS) and Time-of-Flight Secondary Ion Mass Spectrometry (TOF-SIMS) have become powerful tools for characterization of different forms and carriers of gold for the needs of the mineral processing industry. Major advantages of these techniques are related to their ability to analyze individual mineral particles and provide quantitative analysis with detection limits in the low ppm/ppb concentration range. This paper describes various micro-beam techniques and procedures implemented at Surface Science Western (SSW) for quantification and characterization of the sub-microscopic gold and the preg-robbed surface gold as part of full gold deportment studies in feeds and process stream products."

Jan 1, 2014

By I. Blayda

The purpose of this work is to study and make comparative analysis of germanium extraction and related valuable components of the sublimates from the burning of domestic power coals (product 1) and germanium sulfide materials, which are a waste of lead-zinc production (product 2), by traditional chemical methods (distillation of germanium in the form of tetrachloride from raw and preliminary burning source) and by microbial bioleaching of sulfur-oxidizing bacteria. The dependence of the germanium extraction by chemical methods from phase composition of the initial raw materials was installed. The germanium tetrachloride extraction from products 1 and 2 were 78.50 and 19.52%, respectively. Such difference in indexes on extraction, is caused by germanium confinement as concomitant trace component to the basic phases to carriers. The share of acid-non-soluble compounds (tetragonal modification GeO2 and silikogermanaties) in the product 1 account for 21.5 % of germanium. Ratio between acid-soluble and acid-not -soluble germanium forms are 19.52 and 80.48 %, respectively, in the product 2. Our experiments have shown, that implementation of restorative firing (with addition of 30-40 % carbon at 1150 0?) of sulfide product 2 considerably impacted on the extraction of germanium tetrachloride (91.76 %) in comparison with its low enough extraction at straight distillation of hydrochloric acid (19.52 %). The results are confirmed by a set of physical methods. The results of processing the same so-called hard phase?s material (product 2) with the help of microorganisms are presented. It Has been established, that selected strains of bacteria are capable of extracting from initial raw materials not only macro components (iron, zinc, lead, manganese, aluminum, nickel), but also micro impurity of rare metals (gallium, germanium, zirconium). It is important that these metals were not extracted by traditional chemical methods (with application of aggressive conditions and heats) independently of the phase composition of the source. Almost complete extractions of germanium in solution using sulfur-oxidizing bacteria take place in the first day of the process independently of the phase composition of the source and the type strain. The results have practical significance and can be the basis for developing a unified biotechnological method of technogenic waste processing with a purpose of their sterilization and detoxification with simultaneous obtaining concentrates of valuable metals. Keywords: germanium, extraction, sublimates, bioleaching, sulfur-oxidizing bacteria.

Sep 1, 2012

By Valery V. Kostjuk, Victor. N. Bredikhin, Alexander I. Shevelev, Evgeny A. Kazban

"The investigations to improve the process data have been done in order to stabilize the functioning of drying units. The scheme of turnings preparation with centrifuging and subsequent thermal degreasing (tandem) is proposed. To improve the efficiency of the process the scheme of reclamation of the centrifuge fugate is developed with production of oil and service circulating water. Empirical dependences of the turnings temperature influence on the lubricant-coolants content in centrifuging are gained. When the turnings temperature is increased to 80 C the residual content of LC is decreased by 1.5%. The investigations aimed to improve the preparation of non-ferrous turnings have allowed to decrease the melting loss by 15-20%; to stabilize the process of thermal drying of turnings; to decrease sharply (by 60- 70%) the volume of LC combustion products; to reclaim the centrifuge fugate and produce oil and servicecirculating water.Non-ferrous turning and primarily aluminum and copper alloys turning is a stable source of secondary raw materials for metallurgical works.Direct by lubricant-coolants (LC) of various types: synthetic, semi synthetic, oily and emulsions.On the base of investigations concerning various methods of the non-ferrous turning processing the favorable one has been selected taking in to consideration the economy, ecology and quality of the finished product (alloy). Two-stage process is developed. The main idea of the process is the elimination of the lubricant-coolants (LC) to the limit specified in advance. The applied method is centrifuging with subsequent final elimination of LC by thermal method.Constant value of LC content at the inlet of the thermal unit excludes practically the oxidation of metal and as a consequence increases the output by 10 –15 % in metallurgical processing."

Jan 1, 2003

By Milind Sabne, Pradip, P Kapur, Beena Rai

"The efficiency of an industrial flotation circuit depends on (a) the selectivity and the kinetics of the reagent combination selected for the separation (b) the hydrodynamic conditions prevailing in the flotation cell (essentially equipment design parameters) affecting both the pulp and froth phase (c) the operating parameters such as feed rate, pulp density, pH, temperature etc. including the mineralogy, particle size distribution and relative proportion of liberated and composite particles of constituent minerals in the feed to flotation circuit and (d) the circuit configuration itself. We have developed a molecular modelling based reagent design and selection framework to assist mineral engineers to arrive at the preferred reagent combination based on a rigorous, scientific and quantitative comparison of various options available for this purpose. Similarly we have also utilized a general circuit design methodology proposed by Kapur and Mehrotra in 1974. The advances thus made in modelling both the reagent chemistry as well as circuit design, along with the availability of sophisticated, automated tools for characterization of ores (liberation as well as mineralogical composition of the different flotation streams) provides a scientifically rigorous, quantitative, robust framework for design and optimization of complex flotation circuits. We illustrate in this paper the power and the utility of our rigorous optimization based approach to designing industrial flotation circuits for the beneficiation of a multi-component feed with the help of few case studies from our own work. With the proposed methodology, higher levels of process efficiencies can be achieved in the industrial flotation plants, in particular those processing complex, multi-component feeds requiring multiple stages of flotation separation. We are currently developing an IT platform consisting of computer-aided decision support tools for arriving at the preferred flotation circuit and the appropriate reagent chemistry for a given ore deposit and/or a given plant."

Jan 1, 2014

By S. Banisi, O. Farshid, M. R. Rozebehi, A. Bahar, A. Arghavani, M. Mahdavi

At the rougher flotation circuit of the Miduk copper concentration plant (Kerman, Iran) five column cells (CISA) with the diameter of 4m and height of 12m using static mixer type (MicrocelTM) spargers have been installed. Based on the initial design, columns should accept a feed rate of 625 t/h with 80% passing size of 90 µm and solids concentration of 28% and produce 88% of the plant concentrate (i.e., 22 t/h) containing 32% copper. Due to mechanical and processing problems this objective was never realized and theses columns were remained out of operation from the commissioning time (2005). A new attempt with the aim of returning these cells into operation started in 2013. The results of an extensive study indicated that spargers plugging due to the entrance of small amount (2 kg) of coarse particles (up to 2.5 cm) because of usual problems at the plant environment was the main reason of columns non functionality. With a change in the recycle pump inlet design to the column, which prevented the entrance of coarse particles to the spargers, the operation of the column significantly improved. It was found that in order to have a stable operation of the columns at the rougher stage the feed rate for each column should be reduced from 125 (design) to 70 t/h. The air superficial rate had to be also reduced from 1.9 (design) to 0.6 cm/s. A period of 10 days of continuous operation showed that the carrying capacity was 0.23 (g/min/cm2) which was significantly lower that of the design value (i.e., 0.58). The gas hold up was found to be lower than 10% beyond which columns started to move to the turbulent state indicated by "boiling" froth. The average life time of spargers was determined to be 20 days which considered to be very short. The average recovery and concentrate grade of these columns were found to be 68% and 32%, respectively. The high wear rates of spargers, unusually high level of maintenance and supervision needed and instability of the operation made the plant managers not to use column cells as the roughers.

Jan 1, 2014

By Sanggono Adisasmito

"The quality of the higher education in Indonesia is being improved by implementing a program financed by the World Bank under a project named QUE (Quality for Undergraduate Education). The investments are provided to selected study programs through a competitive selection process. The grant finances staff development, the purchase of equipments, textbooks, consumables, technical assistance, and incentives for outstanding faculties such as teaching grants, project grants, lecture note awards, and educational policy studies. These additional investments are provided to produce chemical engineering graduates that will compete beyond the national market.Chemical Engineering Department of Institut Teknologi Bandung in Indonesia has been selected to receive the QUE grant beginning the year 2000 and ending the year 2004. The department is actively involved in the mineral processing issues, particularly in the aspects of energy supply and the environmental protection. The activities are distributed in different laboratories and areas of expertise, such as: thermodynamics and utility systems, process equipment, chemical reaction and catalysis, microbiology and bioprocess engineering, process control, ceramics, as well as polymer and membrane technology. The main objectives of the QUE project are to improve the undergraduate program in the following aspects: Relevance, Academic atmosphere, Institutional management and commitment, Sustainability, as well as Efficiency and productivity, or abbreviated as RAISE. At the end of every fiscal year, the progress of the program is evaluated to measure the effectiveness of the project.The achievement of the QUE project objectives were assessed using performance indicators developed during the program design. There are six indicators to measure the performance of the individual program of study, such as: (1) Admission Test score, (2) average students' Grade Point Average (GPA), (3) average graduates' length of study, (4) graduates' waiting time before getting first job, (5) Test of English as Foreign Language (TOEFL) score, (6) Graduate Record Examination (GRE) score. Essentially, the RAISE evaluation criteria will be used to perform three main functions, such as (1) to measure the achievement through the six quantitative performance indicators, (2) to support the progress of evaluation and reporting throughout the implementation of the program, (3) to provide a universal framework for qualitative evaluation."

Jan 1, 2003

By Lokesh K. Thakur, Peter Radziszewski

"For the cases tested (11 mills with 15 operating conditions), the Bond abrasion test steel media wear rate prediction gives an overall error of 73% and a standard deviation of 192.5%. However, total steel media wear in a given mill (ball or SAG) grinding process is a product of three recognised wear mechanisms -- impact, abrasion, and corrosion. A total media wear model can be defined on the assumption that the effect of each wear mechanism can be independently determined which allows for a total media wear model to be defined as the summation of the wear result of each mechanism (eqn. 1). It is assumed that impact and abrasive media wear is a function of the energy dissipated in impact and abrasion as estimated by a DEM charge motion simulation. Corrosive media wear is assumed to be a function of the media surface area present in a mill.The 3 initial tests developed (steel abrasion wheel, corrosion batch mill, impact chamber) coupled with the impact and abrasion energy spectra from a DEM charge motion simulation produced total steel wear rate results for the same cases as the Bond abrasion test giving an overall error of 0% and a standard deviation of 66.1%. However, if one were to consider the general observation that wear is proportional to energy and maintain the assumption that corrosion is proportional to media surface area then one would realize that the total media wear eqn. (1) can be reduced to eqn. (2). As this is a linear equation and one has, for the same mill, media wear and operating data for three different operating cases, one obtains three equations with three unknowns. This defines a simple matrix manipulation to determine the constants k1, k2 and k3. From the previous data set, we had 6 identical mills grinding the same ore but having different worn liner profiles and charge volume which provided the opportunity to average out the ki values over 20 combinations of 3 cases. With the determined ki values, it was possible to determine a second estimate of the contributions of impact, abrasion and corrosion to total media wear giving an overall error of 0% and a standard deviation of 56%."

Jan 1, 2003

By Peter Ay, Elena Geldt, Satyanarayana Narra, Claudia Glaser

"As part of an extensive research and development project, the technical and technological implementation of the patents DE 10 358 245 B4 and WO/2006/056172 was developed with the goal to present a system for the innovative roll- agglomeration method exhibiting a) a modular setup, b) high productivity and c) suitability for the use of fibres of different applications and product qualities (high technical availability). The processability of the rarely adapted raw fibre materials into high-value intermediates brings forward their application in various processing industries dealing with the production of fibre reinforced plastic composites, heat and sound insulation materials as well as with the gas and liquid cleaning systems. The innovative fibre agglomeration presented in this work is performed by a combination of rolling and pressing the fibres inside a geometrically pre-defined roller table, in which the fibres are forced to bound through entanglement / interlocking and develop into agglomerate. The agglomeration process is carried out in a circular roller path with a rectangular cross-section. For improving the adhesive properties, and thus the quality of the agglomerates, the boundary surfaces can be covered / patterned / lined / coated with various materials. The resulting roll-agglomerates are characterized by different quality parameters such as mass, shape, porosity and stability. The properties of the agglomerates can be modified based on the end-product requirements by slightly modifying the process parameters such as filling ratio, residence time, roll-geometry, procurement of the boundary surfaces, etc. as well as the input material properties such as fibre type, fibre fineness, fibre length, etc. This work carries extensive work on the roll-agglomeration system to assess the effectiveness and the variability based on the product specifications. Agglomerates were produced with wide variations of system parameters with varying roller table liners and based on evaluation of the produced agglomerates with respect to their mass, the geometrical dimensions, their porosity and stability."

Jan 1, 2014