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By S. Banisi, E. Arghavani, M. Pourkani, M. J. Rajabi, Gh. A. Mohamadian, H. Bidshahri, Gh. A. Parsapour

The Sarcheshmeh copper complex flotation circuit of plant No.1 consists of two identical north and south sections where each includes four rougher (each bank consists of 14 cells), two cleaners (each bank consists of 8 cells), two recleaners (each bank consists of 2 cells), and two scavenger banks (each bank consists of 10 cells). The reduction of feed grade along with a change in the mineralogical composition is the main reason of current lower concentrate grade (24%) compared with the design concentrate grade (32%). Because of a lower feed grade, the amount of rougher concentrate has decreased which in turn has significantly reduced the feed rate to the cleaner, recleaner, and scavenger banks. This has increased the mean residence time of the material in the cleaner section resulting in a lower final concentrate grade. A laboratory study showed that the final concentrate grade can be increased by 2-4% if one cleaner stage is added to the flotation circuit. In this research, based on the laboratory results, one cleaning stage was added to the current flotation circuit. In order to make this modification instrumentally possible in the plant, the final concentrate was gravity transported to the Mo-Cu thickeners. This released 2 pumps and associated tanks which made addition of one cleaning stage practicable. Finally, a part of the cleaner and scavenger cells were used as the third cleaning stage. This decreased the residence time in the cleaner and scavenger banks. After implementation of one cleaning stage in the south section of the plant, the performance of the circuit compared with the identical north section. It was found that at the same recovery, the concentrate grade of the south section increased by 2.5%. The promising results led to the implementation of adding one cleaning stage in all sections of the flotation circuit.

Jan 1, 2018

By T. N. Aleksandrova, A. V. Afanasova

"The research is aimed at solving the problem of enrichment of sulphide ores, counting for more than 40% of the reserves in Russia. The aim of the research is to develop and scientifically substantiate the scheme for processing this type of ores in order to extract fine-dispersed noble metal particles (FNMP). In this work samples of sulfide carbonaceous ore and flotation concentrates were analyzed using complex precision methods of analysis: electron microscopy, spectral analysis with induction plasma, complex thermogravimetric analyzes, etc. Data on the composition of the organic constituent of the samples were obtained with the usage of complex thermogravimetric analysis. The presence of various types of kerogen and bitumen has been established. Experimental studies on the coarsening of FNMP from the initial ore and flotation concentrates using electromagnetic radiation have shown the effectiveness of this coalescence method. The data on the elemental composition of the samples and the amount of FNMP were obtained. Thus, studies on the extraction of FNMP from carbon sulphide ore have shown the possibility of effective usage of combination of electromagnetic action and classical enrichment methods to extract fine particles of noble metals. INTRODUCTION Due to the depletion of free-milling raw materials the involvement of new types of deposits is the strategy of developing mining industry of Russia. The black shale raw materials show interest as a non-traditional source of precious metals since its genetic and positional gold-carbon connection. Muruntau, Sukhoi Log, Bakyrchik, Natalkinsky, Nezhdaninskoye, Olimpiadinsky, Homsen and others are the examples of well-known deposits of the black shale formation [1]. In fact the main gold-dispersed regions of Russia are composed of black-shale strata. Review of literature [2-5] shows that in recent years in almost all deposits of the black shale formation metals of the platinum group (PGM) were detected that significantly increases their practical importance."

Jan 1, 2018

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 Hernán Menares, Diego Hernández

"Over the last few years, the copper mining industry has been facing a changing scenario with respect to both the market and society which has resulted in taking a closer look at the way in which mining is being done. The cycle of high metal commodity prices of the last decade left the industry with high costs. Together with increased environmental and social requirements, a decrease in ore body quality, scarcity of resources such as human capital, water and energy, has resulted in an ever-increasing challenge to make a profit out of new ore bodies but also to maintain the current operations in the longer term competitive. The major challenge is to create value for all stakeholders, exploiting ore bodies that nowadays are not considered economically attractive, which applies to both new ore bodies and existing operations, but in a sustainable way. In order to achieve this objective, it is necessary to approach the mining business differently in five main areas: (1) operational efficiency through better use of installed equipment and skilled labor force; (2) efficient use of energy; using opportunities for alternative energy sources and efficient design; (3) efficient use of water; diminishing losses and use of seawater as an alternative source; (4) minimizing environmental impact by eliminating effluents and controlling dust emission; and (5) a more closer, proactive and collaborative relationship with the communities allowing them to be an active player in the solution to assure a sustainable business in the long term. This presentation will show how Antofagasta Minerals is facing these challenges with a long term strategy that includes all of the above mentioned aspects and that is allowing the company to exploit its mineral properties in an efficient and successful way."

Jan 1, 2014

By Gustav Hawlitschek, Henrique Kahn, Carina Ulsen, Renato Contessotto

"The problems related to waste dumping increased with the growth and development of large cities. In the U.K., more than 50% of landfill waste comes from construction use and the U.S. alone produces around 200 to 300 million tons of CDW annually. The exhaustion of natural sand deposits close to large urban centres stimulates the recycling of construction and demolition waste for the production of recycled aggregates as a construction material. This paper presents a flowchart for the production of recycled sand with low porosity and regular shape by the selective removal of the cement paste attached to recycled aggregates. The products characterization was carried out by the determination of the particle size and shape distribution, chemical and mineralogical composition, heavy liquid mineral separation and quantification of all present phases using a scanning electron microscopy with automated image analysis (SEM-MLA). The comminution of CDW by vertical shaft impact crusher made possible the production of a lower porosity recycled sand. The heavy liquid mineral separation showed that the proportion of low porous phases (d>2.5 g/cm3) is very high, exceeding 70% of the weight, encouraging further mineral processing separation to obtain a fine recycled aggregate with less cement paste content. The mineralogical characterization by XRD and SEM indicates that the main phases are tectosilicates, phyllosilicates and calcite which one can be attributed to both calcareous aggregate and cement paste. The precise quantification of cement paste and calcite/dolomite alone is just possible by automated image analysis. The characterization results demonstrated that proportion of phases with no cement paste attached increases progressively in denser products. The results of heavy liquid separations and image analysis are comparable and automated image analysis can be used for the characterization of phase content and their main associations."

Jan 1, 2014

By Olgac Kangal, Ali Guney, Gulay Bulut, Guven Onal, Ayhan A. Sirkeci

"This paper presents the results of pilot scale column flotation applications in the two different copper concentrators in Turkey. The Kure Copper Plant is located in the Black Sea Region of Turkey. There are four types of copper ore formations in the Küre region. The so called disseminated ore contains 60-70% siliceous minerals of which Cu content is around 0.5%. The remaining three ore types in the region are generally named “massive ores”. The massive ores may assay up to 15% Cu and the major gangue mineral is pyrite associated with relatively little amount of silica. The main copper mineral in all formations is chalcopyrite that is generally finely disseminated in pyrite therefore satisfactory liberation requires ultrafine grinding especially in the case of the massive ores.A blend of these ores, containing 1.7% Cu on average, is fed to the Küre Copper Concentrator whose capacity is 1.2 million tons of ore annually. Unfortunately, today the plant operates below its designed capacity treating around 550,000 tons of ore per year. The design of Küre Copper Plant was undertaken by the Outokumpu Company of Finland. The operation of the plant is almost automatically controlled and the feed, the concentrate and the tailings are assayed for copper by on-line XRF analysers. The particle size analysers are also connected to the grinding circuit. The feed material is ground almost below 50 µm and the flotation is conducted around pH 11.2 using Hostaflot X-231 (a trade mark of Hoechst) as the collector. Apart from the rougher cells, there are four cleaning stages after which the final concentrate is produced. A very fine grinding requirement for an adequate level of liberation makes successful flotation difficult and consequently the final concentrate can hardly assay above 16% Cu leading to copper losses around 20% in the tailings that contains 0.3% copper."

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 Kazutoshi Haga, Batnasan Altansukh, Shirchinnamjil Nyamdelger, Atsushi Shibayama, Narankhuu Ariunbolor, Gunchin Burmaa

In this study, the authors investigated the capability of an acidic thiourea solution and silicon-organic polymers (PSTM-3c, PSTM-3T) as ion-exchange resins to recover of gold from gold-bearing ore concentrates. Firstly, elemental gold present in flotation concentrates was dissolved by leaching with a solution of nitric acid and thiourea under the optimized conditions. The best result on gold thiourea leaching was obtained under a nitric acid concentration of 2 N, thiourea concentration of 2 %, and oxidant (Fe2(SO4)3) concentration of 3 %, solid:liquid ratio (S:L) of 1:20, leaching time of 6 hours at 20 °C with a gold recovery of 93.7 % for a gold flotation (unroasted) concentrate. For the roasted gold concentrate, the dissolution of gold was 94.8% under the optimized leaching condition as nitric acid concentration of 0.5 N, thiourea concentration of 2 %, and the oxidant concentration of 1 %, S:L ratio of 1:10, leaching time of 4 hours at 50 °C. Secondly, a series of sorption tests was carried out on a pregnant leach solution containing gold complex Au[S=C(NH2)2]2+ using silicon-organic polymers (PSTM-3c and PSTM-3T), respectively. The effects of solution pH, adsorption time and temperature in the sorption process are also studied. As the results, the PSTM-3c and PSTM-3T polymers were adsorbed about 94.4 % and 95.1 % gold from the pregnant leach solutions under the optimum sorption conditions, respectively. It was found that the both PSTM-3c and PSTM-3T polymers were effective for the recovery of gold from the pregnant leach solution of thiourea. Adsorption activity of the PSTM-3c and PSTM-3T polymers was confirmed by new peaks near 1700 cm-1 in the FT-IR spectrum of the gold-adsorbed polymers, respectively.

Jan 1, 2014

By Komar Kawatra, Joseph Halt

"Bentonite clay has been the traditional binder for iron ore pellets. However, bentonite increases pellets’ silica contents and is expensive. Researchers have proposed lowering bentonite doses by mixing it with other common binders. These mixtures may only be successful if the fundamental bonding mechanisms are understood. For example, what happens when bentonite (physical bonding) is mixed with fly-ash (chemical bonding)? What happens when bentonite is mixed with cornstarch (physical bonding)? In this paper, experiments are described where bentonite was mixed with various ratios of cornstarch and fly-ash, and pellets were agglomerated using 0.66 % w/w binder. Ca(OH)2 and CaCl2 were added as activator and accelerator, respectively, to the bentonite-fly ash mixture. Curves of pellet dry strength vs. bentonite-starch ratio were linear, suggesting the physical-physical bonding mechanisms were compatible - acceptable strengths (> 22 N) were produced at all bentonite-to-starch ratios. This was contrary to bentonite-fly ash mixtures, which displayed dry strength curves with a noticeable minimum due to competing binding mechanisms. Bentonite alone and fly ash alone produced acceptable strengths (> 22 N), but their mixtures resulted in weak pellets. Due to the positive results using cornstarch (CS) binders, the effects of CS solubility in water were investigated using two CS with high and low solubility (60 and 7.5 %). CS was premixed with bentonite at various ratios (0, 20, 40, 60, 80, 100 %). Pellets were agglomerated using 0.66 % w/w binder. The dry strength of pellets ranged from 50-300 N using the high solubility CS mixtures, and from 50-85 N using the low solubility CS mixtures. Fired strengths exceeded 2200 N/pellet at all bentonite-cornstarch ratios. This research showed that cornstarch solubility is an important factor in determining its effectiveness as a binder for iron ore concentrates, but significant work is still necessary before it can be used as a bentonite replacement."

Jan 1, 2014

By A. T. Sutaone

"In the Dongri Buzurg Manganese Mine of M/s Manganese Ore (India) Ltd., high grade lumpy manganese ore required for iron and steel industries is produced through multi-stage crushing and screening. This has resulted in accumulation of 50,000 tonnes of low grade fines over the years. This production of such fines is still going on. The fines create environmental problems, like air and water pollution and siltation in adjoining fields. Besides containing lot of manganese values, they occupy large space which is very scare in mining area.The Indian Bureau of Mines under one of its statutory functions has suggested the company to explore the possibility of recovery of additional values under conservation and environmental aspects. Hence the company has sponsored a bulk sample for beneficiation studies in the Modern Mineral Processing Laboratory and Pilot Plant of Indian Bureau of Mines at Nagpur, India. The main manganese minerals present in these mine rejects have been identified as pyrolusite and psilomelane. The purpose of this study was to explore the possibility of evolving a suitable beneficiation flowsheet to obtain manganese concentrates assaying over 72% MnO2 to be used as raw material for the manufacture of dry cell batteries.The sample/material was subjected to characterisation studies in terms of chemical analysis, granulometry and mineralogical compositions. Based on these characterisation studies, the beneficiation process developed comprised of desliming, jigging and low intensity magnetic separation mainly to reject quartz, silicates and jacobsite. The manganese concentrate thus produced assayed 70.2% MnO2 with MnO2 recovery of 78% and weight per cent yield of 63.5. This natural concentrate could be mixed with the electrolytic manganese dioxide produced by the company and this blend can thus be used as a raw material for the manufacture of dry cell batteries by the end users. The paper deals with the details of test work carried out in evolving the process flowsheet."

Jan 1, 2003

By Vladimir E. Vigdergauz

"Bubble-mineral complexes could be formatted by an attaching of hydrophobic particles to the surface of air bubbles or by an evolution of bubbles from solution onto hydrophobic surfaces. Measurements of contact angles, detachment forces (DF), induction times (IT), evolution pressures (EP) and flotation recoveries (FR) for the studying of minerals wettability at various pH and electrochemical potentials were used. An analysis of the obtained IT results show that a process of bubble attachment to a mineral surface is a rather slow one and it will scarcely be enough for bubble-mineral complex formation under the conditions of real flotation.The ranges of adhesion potentials obtained by DF measurements, Figure 1, correlate with the data of floatability-potential for pyrite. The ranges of adhesion potentials obtained by DF measurements for galena (-1 ÷0.2V) and chalcocite (-0.5÷1.2V) correlate with the potential ranges of floatability for galena (<0.2V) and chalcocite (>-0.4V). An increase of the DF and the cathodic limit of the adhesion potential with increasing length of the hydrocarbon chain were observed. EP-pH curves for sulfides are a mirror-like to the DF-pH curves, Figure 2. Structure of solid-liquid and liquid-gas borders has a determinative importance for formation of bubble-mineral complexes and subsequently flotation results. Under vacuum on the mineral surface there are produced micro bubbles and preferably they will be appeared on the hydrophobic sites. Water structure breaks near a hydrophobic surface facilitate water mass destruction and formation of gaseous phase embryos under decompression in the impeller zone. It simultaneously reduces a probability of produced micro bubbles dissolution as a result of pressure increasing owing to constant fluctuation of liquid densities into impeller zone. Comparison of Taggart’s evaluation of the suction behind blades of the impeller of an agitation-froth machine and ABEP data on galena, Figure, shows that gas evolution will be observed in the range of 1300-2700 revolutions of impeller per minute for hydrophobic and hydrophilic surfaces successively."

Jan 1, 2003

By Andrei Kolesnikov

"The results of CFD modelling of complex heat transfer and fluid flow in DC electric arc furnace are presented. The model includes energy and momentum conservation equations for gas phase (freeboard), liquid phase (molten bath) and solid phase (walls and graphite electrode). Simulation revealed the temperature distribution in all elements of the furnace. The influence of the arc and melt resistance on the temperature distribution is discussed.Computational Fluid Dynamics (CFD) becomes a powerful tool for better understanding of the heta and mass transfer processes in industrial equipment. In current work commercial CFD software STAR-CD was used to analyse complex heat transfer in DC EAF, including forced and natural convection, conduction and radiation. The finite volume solver using body-fitted grid was used. The grids are non-staggered hexahedral grids and all variables are evaluated at cell centers. Steady-state calculations were performed with PISO algorithm. For the convective terms in equations the hybrid differencing scheme was used. An upwind differencing scheme was used for other terms. Conjugative heat transfer was taken into account in heat transfer calculations on gas-liquid and gas-solid interfaces. Radiation from the arc and inner surfaces of the furnace was calculated by a “discrete beam” approach. Source term in energy conservation equation was used to represent heat release in the zone occupied by the DC electric arc. The volume of this zone was calculated from semi-empirical equations. The Joule heat and heat due to chemical reaction in the melt were calculated through the source term expression in the energy balance equations for the slag and metal in the molten bath. The gas acceleration in the electric arc zone and stirring of the slag due to gas bubbles motion were accounted for by momentum source terms in the momentum conservation equations.All simulations were carried out using axisymmetric two-dimensional grid. The grid resolution was 20 cm per cell in most part of the furnace, except the arc region, where resolution was 5 mm per cell."

Jan 1, 2003

By W. H. Cheung

Nickel (Ni) plays a major role in the production of steel and other major alloys. There are two sources of Ni: laterite and sulphide ores. Global reserves of sulphide ores are being rapidly depleted, while there are enormous reserves of Ni laterite, much of it in Australia. As well as being present in huge amounts, Ni laterites have the advantage of containing cobalt (Co), a valuable mineral. Over the past decade, these factors have been driving the industry to explore the processing of Ni laterite. A route that has been used commercially in processing nickel laterite ore involves the thermal activation of the minerals by pre-reduction followed by ammoniacal leaching (Caron). Although this process has been effective in processing the goethite rich laterite minerals, the higher-grade serpentine-based minerals have been shown to be less susceptible to this process. This has been attributed to the formation of inert olivine phases. In this study, we examined the use of an alternative lixiviant, sulphuric acid, in leaching pre-reduced limonite and weathered saprolite nickel laterite ores. The specific aim of this study was to examine the sulphuric acid leaching of Ni and Co from pre-reduced laterite minerals, and to understand the role of mineral transformations in this metal dissolution. Synchrotron based X-ray diffraction was used to examine the transformation of goethite (FeOOH) to spinels and serpentine mineral ((Mg,Fe)3Si2O5(OH)4) to olivine. Reduction tests were carried out using CO and CO2 reducing gas mixtures and temperatures from 400 °C to 700 °C. The rate of formation and disappearance of specific Bragg peaks during reduction of specific minerals were used to derive an understanding of these solid-state reactions. Laboratory based reduction tests and leaching in sulphuric acid were used to validate the effect of these mineral transformations. The results suggest the versatility of sulphuric acid in leaching nickel from spinels and olivine, which was achieved at the expense of lower selectivity. Cobalt dissolution was found to be dependent on the nature of ferro-cobalt alloy formed during reduction.

Jan 1, 2014

By Çisem Tuba, Ismail Girgin

"Comparative atmospheric H2SO4 and H2SO4 + H2O2 leaching experiments were performed using a Turkish lateritic nickel ore containing 1.52% Ni. In the leaching tests; acid concentration, temperature and leaching time were considered as main variables and the dissolution behaviour of the ore were studied by Ni, Fe, Co and Mg analyses. The dissolution values in the H2SO4 leaching experiments were observed to increase up to 60% (w/w) acid concentration and a temperature of 95°C. Increase of H2SO4 concentration above 60% at 95°C caused decreases in all the dissolution values and this was attributed to the formation of Fe2(SO4)3 and Fe2(SO4)3•HSO4•H2O type compounds. At the considered optimum H2SO4 leaching conditions ([H2SO4]= 45%, T=95°C, t=45 min); dissolution values reached for Mg, Ni, Fe and Co were determined as 99.12%, 95.58%, 92.63% and 78.37%, respectively. An activation energy of 30.57 kJ/mole was determined for nickel dissolution from the evaluation of the kinetic data obtained for H2SO4 leaching showing that the dissolution was controlled by external diffusion and chemical reactions. Caro’s acid solutions were prepared at H2SO4/H2O2 mole ratio of 3 for varying initial H2SO4 concentrations and leaching tests were performed at 25°C. Co behaved very differently and a dissolution value of 83.94% was obtained even at 5% acid concentration in 60 minutes reaction time. Complete dissolution of Co was obtained after 30 minutes of reaction time at 60% initial H2SO4 concentration and the corresponding dissolution values for Mg, Ni, and Fe were reached to 96.16%, 94.27% and 89.46%, respectively. Although the H2SO4 + H2O2 leaching experiments were conducted at 25°C, it was realized that the temperature of the leaching medium was increased to 122°C after four minutes of reaction time due to probable exothermic reaction(s) at 60% initial acid concentration."

Jan 1, 2014

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 Alexey P. Tatarinov

Under modern economic conditions in Russia, gold heap leaching is the most effective way of investing into gold-mining industry. Gold is recoverable from small-size deposits, low-grade ores from oxidation zone, cut-off grades, and overburden rocks using heap leaching. This technology is cost-effective and allows a saleable metal to be obtained within the first year of operation. The investments for heap leaching are lower than those of for a traditional plant technology. Production cost per one gram of Au is 5-7 times lower than that of during a plant flow sheet. A seasonal development of mines can be possible. With reference to this, heap leaching resembles the technology of placer deposits development. One of the major advantages of heap leaching is the form of the product. Gold can be obtained as dissolved in a clarified PLS, which allows the further quick treatment. The amenability of ores to heap leaching depends on their mineralogical composition. Oxidized porous ores with a good access of a lixiviant to valuable particles can be treated without pre-crushing. Clayish minerals are often found in oxidized ores with free gold. In order to build ground for heap, several major methods combined with various pad materials are used. These methods have been used at many plants and are reliable. The development of heap leaching technology for gold ores for the deposits from Yakutia, Zabaikalsky region, Primorye region, Uzbekistan, Tadjikistan, and Kazakhstan began in the 70s. However, it has been commercially used only since 1990. The first heap leach plants were built and commissioned in the USSR in 1991 at Vassilkovsloye deposit (Kazakhstan) and at Maiskoye deposit in Russia in 1994. Pilot plant testing was conducted in 1996 using ores from Kuranakh ore field, deposits Phiskulturnaya-Kholodnaya and Lopukhovskoye from the Aldan region. After the first successful commissioning of heap leaching plant in Russia, this technology has been commercially applied for deposits. Every year 1-2 heap-leaching plants were commissioned. More than 30 heap-leaching plants have been commissioned both in Russia and in the former Soviet Union using technologies developed by IRGIREDMET. Keywords: cyanide leaching, heap leaching, ore, percolation, solutions, lime technology

Sep 1, 2012

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 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

By R. Weyhe, B. Friedrich, H. Heegn

"Nickel-metal hydride batteries (Ni-MH) are storers of electrochemical energy, which have a higher specific storage capacity than lead or nickel-cadmium batteries. The demand for Nickel-metal hydride batteries is increasing rapidly since their market launch in the early 1990's. In 1999 the output of cells exceeded 80,000 tons per year (1 billion cells per year). Today there is no suitable and sustainable recycling process to recover nickel, cobalt and rare-earth metals. The discarded batteries are used in the steel industry as alloy material because they contain nickel. Cobalt and rare-earth metals are lost; they are non-recycleable.In a German governmental funded research project, IME Aachen, ACCUREC Mühlheim and UVR-FIA Freiberg are cooperating in processing as well as in creating a feasibility study. The target of this project is the development of a new recycling process for metal recovery from Ni-MH-batteries. The proposed process consists of a combination of mechanical, pyrometallurgical and hydrometallurgical processing steps.After shredding the steel shell, the various fractions of battery materials are carefully separated by mechanical processing. A hammer mill with one rotor with a perforated discharge grid of 20 mm opening, was found to be suitable for crushing the batteries to release the active mass of electrodes for metallurgical processing. The ground material is wet screened at a mesh size of 0.5 mm; thus a fine fraction is obtained with valuable components such as Ni, Co, and RE and an oversized fraction consisting of a mix of iron chips, electrodes grids, plastic chips, paper, and flocculent material of separators. The organic components are avoidable when there is a thermal step at the beginning of processing batteries.The separated fine fraction is smelted in an electric arc furnace. Any pyrometallurgical process relies on a suitable slag system. In this specific case, the process has to allow separation of nickel and cobalt as metal from the rare-earths almost quantitatively, collecting the rare-earths as well as impurities e.g. as oxides. The products are a nickel-cobalt alloy and a slag phase enriched with rare-earth oxides for further treatment to ‘mischmetal’."

Jan 1, 2003

By John A. Rumball, Martin R. Houchin

"For gold leaching of oxide ores, the optimum cyanide : oxygen ratio is approximately 106 mg/L NaCN : 10 mg/L O2 (6.9:1 by mole). In sulphide ores, galvanic coupling of the gold with the electrically conductive sulphides significantly increases this ratio such that leaching may occur in a relatively low dissolved oxygen (DO) environment.RESULTS AND DISCUSSIONGold leaching in a carbon in pulp (CIP) and carbon in leach (CIL) circuit is driven by the supply of cyanide and oxygen, as described by Elsner’s equation (1):• 4Au + 8CN- + O2 + 2H2O ? 4Au(CN)2 - + 4OH- (1)Equation 1 suggests that the ideal molar cyanide : oxygen ratio should be 8:1, or 122.5 mg/L NaCN to 10 mg/L of DO. It is generally accepted however, that oxygen is not completely reduced to hydroxide at the gold surface, and that equation (2) better represents the gold leaching reaction (Marsden and House, 1992):• 4Au + 8CN- + 2O2 + H2O ? 4Au(CN)2 - + 2OH- + H2O2 (2)Additionally, since gold leaching is limited by either the diffusion of cyanide or oxygen to the gold surface (Habashi, 1993), then the relative diffusion rates of cyanide and oxygen must also be taken into account. Marsden and House (1992) suggest that the ideal molar cyanide : oxygen ratio is 6:1, while a more recent investigation using laboratory and plant observations (Heath and Rumball, 1998) suggested a molar ratio of 6.9:1.In practice, although a cyanide : oxygen mole ratio of 6.9:1 applies to some circuits, there are many instances when this is not the case.In sulphide ores, galvanic coupling of the gold with the electrically conductive sulphides significantly increases this ratio. Galvanically connected sulphides, and possibly carbon, provide a large surface area for oxygen reduction. As the cathode surface area increases, the oxygen concentration required to sustain the same rate of gold oxidation decreases proportionately.Galvanically connected particles may be composite particles, however they may simply be liberated sulphides in the same suspension as the gold. Particle collisions within a slurry are sufficient to provide momentary galvanic connection (Greet, 1995)."

Jan 1, 2003