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By Z. T. Yuan, S. L. Qi, Q. Y. Meng, G. X. Zou, L. X. Li, J. W. Lu

"The selective separation of pentlandite from serpentine was investigated using the magnetic coating-magnetic separation by conditioning slurry pH value, stirring speed, magnetic field intensity and controlling dosages of sodium hexametaphosphate (SHMP) and sodium oleate (SO). The optimal conditions were obtained as follows: the natural pH of 6.8-7.2, stirring speed of 2300 rpm, magnetic field intensity of 200 kA m-1, SHMP of 60 mg L-1, and SO of 400 mg L-1. Results showed that the Ni grade was 21.4% with the Ni recovery of 81.4% and MgO content of 3.8%. FTIR indicated that coagulant of SO preferentially adsorbed onto pentlandite and magnetite particles while hardly adsorbing onto serpentine particles when dispersant of SHMP was used. Thus, the selective magnetic coating of magnetite on pentlandite surfaces could be formed due to the formation of hydrophobic surfaces on pentlandite and magnetite particles. Calculations of DLVO (Derjaguin-Landau-Verwey-Overbeek) confirmed that interactions between magnetite and pentlandite particles were much stronger than that between magnetite and serpentine due to the existence of hydrophobic interactions with the addition of SO. Consequently, the pentlandite was successfully separated from serpentine. Therefore, this study exhibits the potential to separate pentlandite from serpentine minerals for practical applications and thus deserves further study.INTRODUCTION It has been well known that the separation of pentlandite from serpentine is a worldwide challenging issue in the processing of sulphide nickel-copper ores. Because the serpentine mainly causes the high pulp viscosity and slime coating on the pentlandite, which interferes with the flotation process of pentlandite (Cao et al., 2016; Feng et al., 2012). The fibrous mineral of serpentine preferentially attaches to the air bubble, forming bubble-macrofibers aggregates, which are easily floated into the nickel concentrates, resulting in the decline of Ni grade (Alvarez-Silva et al., 2016; Kusuma et al., 2014). In addition, the serpentine adheres to the pentlandite as hetero-aggregation or slime coating via the electrical interaction between a positively charged serpentine and a negatively charged pentlandite, which decreases the hydrophobicity of pentlandite and reduces the collector adsorption (Feng et al., 2013). In other words, the presence of serpentine or the occurrence of aggregates (including slime coating and bubble-macrofibers aggregates) seriously affects the flotation process and deteriorates the flotation of pentlandite. Therefore, we propose magnetic separation to recover pentlandite from serpentine with the magnetic coating technology, which is different from forth flotation."

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 M. R. Robben

Carbonates have gained significant economic importance for the human kind. On one hand over a hundred uses are listed for carbonates. On the other hand, carbonates host base metal deposits. Although the carbonates play a significant part in the development of those deposits, in the mineral processing they consume acid and cause selectivity problems during flotation and leaching. Carbonates also accompany other industrial minerals as waste rock. For all those cases it necessary to find a technique to separate carbonate as early as possible in the processing chain. In this paper, the applicability of near-infrared spectroscopy (NIRS) sorting for the separation of carbonates is discussed. NIRS sorting is a sensor-based sorting technique, in which particles are singularly detected by a sensor and then rejected by an amplified mechanical, hydraulic or pneumatic process. This technique can for example be implemented in the process as a pre-concentration step for coarse particle sizes up to 300 mm. NIRS sorting discriminates among materials based on the difference that exist between their spectral properties in the near-infrared (NIR). Vibrations of molecular bonds in carbonates cause characteristic spectral properties in the NIR, which makes carbonates detectable, possible to identify, distinguish and separate from other rock materials. The spectral properties can also be used to distinguish between different carbonate minerals and mixtures. If the spectral variations are large enough for detection, sorting based on NIRS is possible. Feasibility studies on sensor-based separation of carbonates in the processing of talc, borate, fluorite, marble, zinc-oxides, copper sulphide and iron ore as well as the discrimination of calcite and dolomite mixtures are conducted and indicate the high potential of NIRS sorting in the minerals industry. Keywords: carbonate separation, sensor-based sorting, near infrared spectroscopy, NIRS sorting

Sep 1, 2012

By Rainer M. Lotzien, Michael J. G. Battersby, Jan Kleefeld, Julian V. Brown, Rainer M. Imhof

A new flotation system has been developed to improve the generally slow separating differentials of fine bubbles and fine particle suspensions. The new technology is based on established pneumatic flotation designs called Imhoflot which use intensive in-line pre-aeration to aerate the flotation pulp prior to its introduction to the separating cell. In the new system (see figure 1) this separation is speeded up dramatically by the introduction of centrifugal motivation in the separating vessel, without the use of internal moving parts. The design focuses on providing increased differential forces on buoyant mineralised bubbles and hydrophilic fines. The commercial benefit to industry is much reduced residence time, less than 30 seconds, which offers considerable cost savings in equipment and infrastructure.

Jan 1, 2003

By Naoki Hiroyoshi, Hajime Miki, Tsuyoshi Hirajima, Masami Tsunekawa

"Acidic solutions for chalcopyrite leaching contain cupric, ferrous and ferric ions, and the oxidizing power of the solutions is indicated by a redox potential, determined by the concentration ratio of ferric to ferrous ions. This paper reviews our previous studies on the redox potential dependence of chalcopyrite leaching in sulfuric acid solutions. Leaching experiments indicated that copper extraction rate was accelerated by cupric and ferrous ions , and was higher at potentials below a critical value (critical potential) in the presence of these ions. This was in good agreement with the results of electrochemical measurements, i.e. in the anodic polarization curves for a chalcopyrite electrode, active-passive behavior was observed when cupric and ferrous ions co-exist, but the activation at low potential did not occur without these ions (Figure 1). The analysis of the AC impedance spectra for chalcopyrite electrode indicated that a high-resistance passive layer grows on the chalcopyrite surface without cupric and/or ferrous ions, and that coexistence of these ions causes a formation of another product layer and inhibits the passive layer growth at low potentials.These results are explained by a reaction model assuming the formation of intermediate Cu2S due to chalcopyrite reduction and the subsequent oxidation of the Cu2S. The critical potential corresponds to the redox potential of the Cu2S formation and the predicted values matched with the experimental results. Catalytic effect of silver ions on chalcopyrite leaching was also discussed based on experimental results and the above model."

Jan 1, 2003

By U. A. Peuker, A. Grohme

"The cost effective and sustainable production of high purity rare earth elements is still challenging. The most commonly used method, known as solvent extraction, is very complex, needs many steps to separate the rare earth ions in a high purity, and causes a lot of environmental problems. An alternative method is the utilization of a separation column filled with adsorbent material. Within the column the desired target substance can be selectively separated out of a multi component mixture in one step. To find out if an adsorption material is suitable for the separation with a column, a characterization of the adsorbent material is necessary. In this paper are described the usage of modified activated carbon (oxygen and phosphorous modification), Di-(2-ethylhexyl) phosphoric acid (D2EHPA) impregnated Amberlite® XAD 7 HP and Lewatit® VPOC 1026 as adsorption materials. Several adsorption isotherms and process conditions are determined to characterize the selectivity between the adsorption materials and different rare earth ions. With these isotherms the mass specific rare earth ion retention for the adsorbent materials can be calculated. In addition to the isotherms the best working parameters are investigated e.g. pH-value and the time for equilibration. Finally, the separation factors between two rare earth elements are determined. The separation factor shows how successful a two element system can be separated."

Jan 1, 2014

By D. Bastin, J. Frenay, J. Dassas

"The Luiswishi deposit belongs to the Cu-Co deposits of the Southern Group of the Katangian Copper Belt and is operated by a joint venture between EGMF (Entreprises Générales Malta Forrest) and Gecamines (Générale des Carrières et des Mines). The Cu-Co ore is beneficiated by the sulphidization process at the NCK (New Concentrator of Kipushi) at Kipushi.Sulphidization followed by flotation with sulphydryl collectors is a common practice for the treatment of oxidized base metals ores. This process is complex and its application at the industrial scale is quite sensitive. In Central Africa it is also a cost intensive treatment as the sulphidizing agent has to be imported. In order to improve the metallurgical performances and to optimise the economics of the process, a laboratory research program was carried out by the Laboratory of Metallurgy and Mineral Processing (MTM) of the University of Liège in close collaboration with EGMF and Gecamines. This program included the study of various flotation reagents as dispersing, depressing and activating agents.This paper presents the results obtained with the use of ammonium sulphate as activator of the sulphidized xanthate flotation. Although ammonium sulphate has been mentioned in the literature as a promoting agent of the sulphidized xanthate flotation of malachite, its effects on the flotation of cobalt oxides was not known.The testworks were carried out on various oxidized siliceous ore types from the Luiswishi deposit. A 1.7 l Agitair laboratory flotation cell was used. NaHS and potassium amylxanthate were respectively choosen as sulphidizer and collector. A mixture of gasoil and tall oil (90/10) was used as secondary collector. A multistage sulphidization was realised. Values of pH were followed during the different tests and an ion selective electrode Ag/Ag2S was used to control the Es potentiel evolution during the stepwise addition of the sulphidizer."

Jan 1, 2003

By Xiaoping Xu, Tiansong Dong, Guosheng Wang

"Jianfengpo tin ore is located in Jiangxi Province, China. The cassiterite is fine and dispersed. It is hard to separate marmatite from a variety of sulfide minerals. Because the iron-containing sulfide minerals including pyrrhotite, pyrite and chalcopyrite are detrimental to the improvement of the grade of zinc concentrate. Besides, the presence of the iron oxides and ferro-carbonate minerals results in the difficult beneficiation of tin. Therefore, Jianfengpo tin ore is a kind of refractory cassiterite polymetallic sulfide ore. According to the properties of Jianfengpo tin ore, the technology process of "Sulphide ore preflotation-Bulk flotation of sulphur and zinc-Separation of sulphur and zinc -Magnetic separation-Gravity concentration" was developed to recover the valuable materials including marmatite, pyrite, magnetite, cassiterite and indium comprehensively. For the feed ore containing 0.87% Sn and 0.70% Zn, a zinc concentrate of 44.56% Zn with a recovery of 69.10%, a high-grade tin concentrate of 54.38% Sn with a recovery of 53.03% and a low-grade tin concentrate of 6.54% Sn with a recovery of 1.25% can be achieved in the batch flotation tests. In the industrial tests, for the feeding which contains 0.55% Sn and 0.65% Zn, the tin concentrate of 49.10% Sn with a recovery of 48.52% as well as the zinc concentrate of 45.11% Zn with a recovery of 60.10% can be produced. Thus some pyrite and magnetite concentrate are recovered as well. So Zinc, tin, sulphur and iron ores are recovered effectively by the technology."

Jan 1, 2014

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 Sergey Gudkov, Yuri Yemelianov, Stanislav Balikov, Andrey Boldyrev, Andrey Bogorodsky

"The results of POX of refractory gold-bearing concentrates using halide-ion as a lixiviant for precious metals and activated carbon as an adsorbent are given. It was found that gold did not recover to the solution when halide was added during POX. Silver partially dissolved in the solution. When halide-based reagents and activated carbon were added during POX, gold dissolved and loaded onto the activated carbon. The degree of sulfides oxidation was 99.3-99.6%. The recovery of gold onto granulated carbon was 94.7-94.8% when using chlorine-bearing lixiviants: NaCL, CaCL and carnalite and 98-99% when using KJ and KBr. This treatment process of refractory gold-bearing concentrates combines sulfide oxidation, dissolution and adsorption of precious metals. The results of the metals recovery achieved using this process can be compared with the recovery during POX-cyanidation. In this case, sodium cyanide was not used. This allows the reduction of capital and operational costs due to the absence of cyanidation, CIL and detoxification of leaching tailings circuits."

Jan 1, 2014

By Ray Everson, Henry Kasaini

"Adsorption of Pd (II) anions on the surface of activated carbon (Norit 0.8) occurred at high proton concentration (0.01 – 2.5M, HCl) in the feed and averaged 27 mg/g. The adsorption process was interpreted in terms of surface ionisation and adsorption model. Enthalpy of adsorption averaged 0.4 kJ/mole indicative of an instantaneous physical adsorption process. We found that the Toth isotherm fit the adsorption data fairly accurately. A combination of the Langmuir and Freundlich equations yields an effective three-parameter Toth equation (1) which is frequently used to describe adsorption on heterogeneous surfaces.Figure 1 shows the comparison between experimental results and the model isotherms. We found that Langmuir isotherms underestimated the adsorption capacity on the porous surface while the Freundlich isotherm overestimated adsorption. Furthermore, the surface coverage at equilibrium was well described by both the Langmuir and Toth isotherms. But, Freundlich isotherm predicted a surface fraction coverage that was higher than unit. Based on better prediction of surface coverage and a reasonable fit to adsorption data, we concluded that the Toth isotherm best described the adsorption data of palladium. The adsorption process was limited by mass transfer resistance through the external film. We estimated the rate constant from equation (2), where e, ?b, and rp are porosity, fluid density and particle radius, respectively"

Jan 1, 2003

By Markus A. Reuter, Antoinette van Schaik

"INTRODUCTIONGoods and products, such as passenger vehicles, are manufactured by using a wide spectrum of different raw materials to meet highest consumer requirements during use. Due to the time-varying composition and complexity of multi-component products such as cars, recycling is complicated. It involves a network of interconnected processes and material and energy flows. Improving the efficiency of the material cycle of the car to comply with the recycling targets as imposed by EU legislation, requires insight into all aspects influencing the closing of the material cycle (dynamics, technology, economy, legislation, etc.) and their mutual relation. In order to define the link between recycling end-of-life products, their changing composition and design a dynamic model was developed for the resource cycle of cars. The model integrates the optimisation of the material cycle with the dynamic behaviour of recycling systems."

Jan 1, 2003

By Stefan Mutz, Thomas Pretz, Jörg Julius, Frank Hilbk-Kortenbruck, Aachen, Hartmut Harbeck

"The annual global production of primary aluminium was about 22 million tons in the year 2000. This represents the second largest production rate in the world market after steel. Experts are predicting that the global demand for aluminium will rise in the near future.In contrast to other metals such as copper, the recycling of aluminium is considered relatively difficult. There are two main alloying groups, namely cast and wrought. In the case of aluminium it is important that the constituents within the scrap aluminium to be smelted are clearly identified. Within the secondary remelting process alloying does take place, but a removal of unwanted metal constituents is problematic. Therefore mixed aluminium scrap (not genuine in-house collected material) can only be used to produce cast aluminium. Thus, in other words a down-cycling of wrought (extrusions and rolled) products occurs. However, in spite of these difficulties there is an increasing trend to produce aluminium from secondary scrap (approx. 35% in Germany). Similar trends have been identified in the USA and other industrialised countries. This development is mainly caused by the high energy consumption for the production of aluminium from bauxite. Producing aluminium from scrap is saving about 95 % of the energy in comparison to the processing of primary raw materials.An improvement in sorting technology is necessary to separate wrought and cast alloys of aluminium as the absolute amount of recovery from old scrap is higher than the demand for cast.This contribution presents some alternative methods, utilizing automatic picking technologies, which will be used to separate secondary aluminium in the future. During the recent years, some major progresses have been made in automatic picking technologies for different applications in the processing of primary and secondary materials.For the sorting of aluminium scrap a special additional sensor will be necessary. The best detection will ultimately be based on online elemental analysis of single particles. First investigations in the field of laser based systems for these applications have already been performed several years ago. One of the laser based techniques is the laserinduced breakdown spectrometry (LIBS)."

Jan 1, 2003

By A. N. Zagorodnyaya, T. N. Bukurov, Z. S. Abisheva, A. S. Sharipova

"This work presents the results of the development of a flowchart for the processing of copper production dusts resulting in the production of of lead sulphate, tribasic lead sulfate (TBLS), ammonium perrhenate, zinc, copper-cadmium cake.Dust having the following composition (wt. %): Pb 39.3, Zn 6.5, Cu 5.5, Stotal 10.8, As 1.05, SiO2 0.6, Cd 0.8, Bi 0.04, Ag 0.02, Re 0.03 was used in the work. Chemical and X-ray analyses indicated that lead, zinc and copper are generally present in dusts in the form of sulfates, various amounts of oxides, sulfides, silicates; sulfur (according to chemical analysis data) is present in the form of sulfates (~ 90%) and in the form of sulfides (~ 10%).Studies have been made on two-stage stripping of copper production dusts containing lead, zinc, copper, cadmium, rhenium in the form of various compounds, at first with soda solution, then with nitric acid solution. It has been indicated that the combination of the operations allows the recovery of 98% rhenium, 82% lead, 92% copper, and 96% zinc and cadmium each in the solution. Furthermore, at the stage of dust leaching with soda, 80% of rhenium and 0.01% of nonferrous metals each are recovered in the solution. Remaining quantities of all metals are recovered in nitric acid solution up to maximum values. Such behaviour of metals is caused by metal phase content in dusts and properties being formed during leaching of compounds. At the stage of dust leaching with soda solutions, carbonates with various compositions are formed due to the exchange reaction between nonferrous metal sulfates and sodium carbonate. The conversion of PbSO4 into PbCO3 is apparently occurs in the solid phase and the conversion of readily watersoluble zinc, copper, and cadmium sulfates into that of carbonate salts occurs in the liquid phase. Rhenium passes into solution due to the presence of rhenium greater quantity in dust in the form of readily soluble perrhenate. Some portion of the perrhenate is, probable, blocked by lead sulfate and liberated in the conversion of PbSO4 into PbCO3."

Jan 1, 2003

By C. Suazo, N. Mora

"The bubble size distribution plays a fundamental role in flotation kinetics. Nowadays it is possible to measure the bubble size distribution, gas holdup and superficial gas velocity by using specialized equipment developed for this purpose. In this article a methodology is presented for estimating the kinetic rate constant using a known particle and bubble size distributions. The attachment and detachment probabilities were modelled from three matrixes. The first matrix represents particle size distribution, the second was named the probability matrix, and the third is the bubble size distribution. Using laboratory data, it has been possible to estimate the flotation rate constant as a function of operating conditions and both the bubble and particle size distributions. The model tested at laboratory scale achieved a quadratic correlation coefficient equal to 0.97. This methodology could be used in the operation and control of the flotation, when in the near future we have industrial equipment that allows in-line measurement, in real time, of gas dispersion and bubble size distribution. knowing particle size distribution, it will be possible to manipulate the operating flotation cell conditions, in order to modify the bubble size distribution and find the bubble distribution that maximizes flotation kinetics. Furthermore, knowing the bubble size distribution, the grinding operator will be able to look for the particle size distribution that produces the maximum flotation kinetics. In order to do this, the operator will have to modify the solids percentage fed to the hydrocyclone cluster, modify the apex/vortex ratio, etc. Finally, this article shows that the maximum flotation speed is reached when the particle size distibution slope is equal to the bubble size distribution slope."

Jan 1, 2014

By Shuji Owada, Mayumi Ito, Idemitsu Kosan Co. Ltd., Takehiko Nishimu, Sadayuki Shinozaki, Takashi Ando, Tomoe Ota

"fElectrical disintegration (ED) by high voltage electrical pulse is a relatively new technique which was demonstrated by Tomsk and Mekhanobr in the 1960’s and has been investigated in detail by Andres in the 1990’s. In the ED, the electrodes should contact to the targeted material and the energy of high voltage pulse is charged directly to the material. It has been reported that the ED is quite efficient to improve liberation of composite materials, because electrical current passes often through the conductive part and/or along the phase boundaries. Theoretically, the energy required in the ED should be lower than in the other mechanical breakage methods, because breakage occurs basically by tensile strength in the ED while in the other mechanical methods it does mainly by compressive strength which is generally ten times or higher than tensile strength.Coal, involving many kinds of mineral matters, is considered to be one of the targets for the ED to apply to. In Japan, national “Hyper-Coal Project” is now running, in which ultra-clean coal (less than 200ppm of ash, 0.5ppm of Na and K, and 2ppm of Ca) is planned to produce by combining advanced coal preparation and liquefaction technologies for the purpose of direct injection of coal combustion gas to turbine. The ED is one of the major techniques to be developed in this project, since mineral matters must be liberated before introducing to the following advanced separation processes. Liberation is important also for the utilization of middling coals generated from usual coal preparation plants. The application of the ED to the middling coals is considered effective for upgrading these coals with higher liberation degree and less energy input."

Jan 1, 2003

By M. Özer, G. Önal, F. Arslan

"The use of ultrasonic in industrial processes has increased during the last few years. Ultrasonic vibrations are used in sieving, grinding, ore washing, cleaning, and flotation in mineral industry. There are also some attempts for the utilization of ultrasonic treatment in separation and removal of fine particles from gases and liquids. In Kalemaden A.S. (Turkey) four different types of clay mixtures (1. A mixture of clays from Balikesir-Düvertepe and Istanbul-Sile, 2. A mixture of clays from Ukrania and Balikesir-Düvertepe, 3. Sögüt-Kadikelimesi, 4. A mixture of clays from Sögüt and Istanbul-Sile) and kaolin from Balikesir-Düvertepe (Turkey) are concentrated before their use in ceramic production. Dewatering is the important step in those types of concentration plants. Sedimentation of concentrated clay has always been difficult and taken long times due to their nature and having small particle sizes. Flocculants can be used to enhance the sedimentation, but they are not preferred by the ceramic industry since they affect the quality of ceramic products. For this purpose, ultrasonic treatment is used in the sedimentation of clays mentioned above for solving the problems encountered related to the ceramic industry and promising results were obtained.Kaolin sample, subjected to this experimental study, from Balikesir-Düvertepe region of Turkey was brought from the plant as a pulp in containers and throughly mixed with a stirrer before sedimentation experiments. A two liter graduated cylinder and an ultrasonic bath (with 25 kHz frequency and 0.5 KW power) were utilized in the tests. Superfloc A-120 (1% concentration) was used as a flocculant. The settling distance was reported against the settling time during the experiments. Initial and final pulp densities were also determined. The effects of several parameters such as pulp density, flocculant addition, and ultrasonic treatment on the sedimentation of kaolin were investigated and the results are represented in terms of settling distance versus settling time."

Jan 1, 2003

By Gülay Bulut, Mustafa Özer, Yunus Emre Benkli, Olgaç Kangal, Istanbul Technical University, Mustafa Tarkan

"Zeolites are naturally occurring as hydrated aluminosilicate minerals. They belong to the class of minerals known as “tectosilicates” and are related to the common minerals feldspar and quartz. Seven natural zeolites that occur in large, commercially exploitable deposits, are: clinoptilolite, chabazite, mordenite, phillipsite, erionite, analcite, and ferrierite. Among them, clinoptilolite is the most abundant one and is not the best known, but is one of the more useful natural zeolite. Clinoptilolite [(Na3K3) (Al6Si30O72) 24 H2O] is very closely related to heulandite and is currently being considered for disuse it self as it may just be a variety of heulandite. It differs from heulandite significantly only in its enrichment in potassium and slightly more silica and it is argued that a separate mineral is not needed.There are large zeolite deposits in western part of Turkey. The sample used in this study was taken from the Gördes region of these deposits. Screen, chemical, XRD and mineralogical analyses were used to determine properties of the natural zeolite sample used in this work.According to the size distribution of the sample, it is found that the zeolite sample used in this study is below 1 mm in size and almost 80% of it is below 0.5 mm. X-Ray Diffraction (XRD) and mineralogical analyses show that the natural zeolite is found to be in the forms of clinoptilolite and heulandite. Clinoptilolite forms as a devitrification product of volcanic glass in tuffs. Quartz, clay minerals, orthoclase, plagioclase, biotite, seruzite-muskovite and epidote were observed as impurities. XRD analysis also shows that the sample contains approximately 58-60% clinoptilolite, 5% quartz, 5% feldspar, 10% smectite, 5- 10% illite and mica and remaining volcanic tuffs. Several types of mineral processing methods were performed in order to remove impurities from the natural zeolite sample to produce high purity zeolite. Gravity separation methods such as shaking table and superpanner were carried out for separating heavy minerals, while high intensity dry magnetic separation was used for discarding magnetic minerals."

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 A. D. Shuloyakov, G. A. Finkelstein, V. I. Kurets, A. K. Vedin

"In disintegrating solid ores with mineral values disseminated in them, one of the principal tasks is to selectively separate valuable mineral particles from the matrix in which they reside, striving at the same time to keep their natural shape and size as intact as possible.The conventional mechanical disintegration methods do not meet this most important requirement in full. The other major objective here is to reduce electric power consumption during the fragmentation stage, since up to 65 per cent of the total power consumption at concentrators processing ores of non-ferrous, ferrous, rare, and precious metals is spent on disintegration steps.Numerous experiments conducted on dozens of ore types (tin, tungsten, and many others, as well as on rock containing diamonds, rubies, emeralds, etc.) have invariably demonstrated by far superior integrity of mineral values as compared with that obtained by mechanical as well as other types of disintegration.However, the process remains as power-intensive as ever which is due to the imperfect nature of the electro-technical devices that convert the network electric current into high-voltage electric impulses responsible for the disintegration process.The maximum capacity attained in disintegrating the hardest materials from 40 mm to 2 mm size in a single operating chamber with four high-voltage electrodes does not exceed 1.0-1.5 t/h. Attempts at increasing the number of electrodes and the capacity of the operating chamber have failed so far because of high overall dimensions and mass of the electrical part of the installation supplying the chamber with pulsating current, as well as of the commutation requirements. At the same time, a number of overseas operations have reported a significant breakthrough in their attempts to reduce dozens of times the overall dimensions and mass of the discharge impulse generating installation (EIS), which enables us to contemplate to increase the capacity of the EIS at least ten times in the nearest future. Yet, even with the currently achieved capacity of the EIS, these installations have found wide use in geological surveying, precious and semi-precious stones production, in grinding super hard materials, etc., since they provide spectacular selectivity of disintegration and thus the integrity of valuable mineral crystals."

Jan 1, 2003