Search Documents

By Jorge Misle, Daniel Silva

"This paper addresses the need for advanced control technologies and strategies in the mining industry, its potential and actual impact on mining processes and the best practices for their implementation, operation, and long term sustainability. It is well known that advanced process control (APC) can be a very good source for incremental process improvement for the mining industry, yielding to higher production rates or helping maintain consistent production rates despite ore changes. The application and integration of new technology, process knowledge and innovation are key elements in building such a supporting structure. More specifically, and this cannot be emphasized enough, the correct application and assembly of control tools, the in-time presentation of key data to decision makers and the development of relevant statistics and KPI’s (key performance indicators) can and will make a difference not only in terms of production, but also in plant stability, availability and production costs. In deploying such ideas and aiming at the long-term goal of "Operational Excellence", Minera Los Pelambres (MLP) has developed a number of successful control strategies, best practices and technologies, which are not only the application of state-of-the-art automation and computing tools, but rather the assembly of the above presented structuring factors. This work discusses some of the key tools and ideas implemented for SAG & Ball milling and Flotation areas, their performance results and the roadmap taken for the integration of process knowledge and control tools. Also, cases studies are presented and discussed further to not only show the main areas of improvement, but also to highlight the benefits of such strategy that for the most part, deviate from the traditional mining industry control approach. Also, a word is given on the need for innovating in the design of control strategies and leveraging best practices and process knowledge that ultimately, will contribute to long-term reliable operations, improved mineral processing and, although unmeasured, lead to a superior overall performance and productivity of all mining personnel involved."

Jan 1, 2014

By Felix M. Zhuravlev, Vitalij P. Lyalyuk

"While there is a large industry based on recovering platinum group metals (PGM) from complex sulphide ores containing Cu and Ni, there is little information on the thermodynamics of the matte phase formed on smelting the ore and in particular the behaviour of Pt in the matte.The equilibrium between metallic platinum and industrial mattes was studied in a series of experiments where a small quantity of matte (5g) and platinum foil of 150 µm thickness (0.5 g) were equilibrated in magnesia crucibles at 1400°C under conditions where the oxygen and sulphur partial pressures were controlled.The chemistries of the phases were determined from EDS analysis using a scanning electron microscope. Line scans were initially used to confirm that the foils had attained a uniform composition across their thickness. The composition of the matte was determined from analysis of an area of matte including the small metallic droplets and dendrites.The distribution of Pt in Cu-Fe-Ni mattes (Pt: 1.5 – 3%) and solid Pt alloys (Pt: 54 – 72%) was studied. For a matte of base composition 45%Fe, 11%Ni, 8% Cu, at a base temperature 1400°C, the following behaviour was observed for the Pt distribution ratio:Under the range of sulphur and oxygen pressure of this study (log pO2 from -15 to –12.2, log pS2 from – 4.6 to –2.2), the distribution ratio of Pt between matte and alloy was independent of the sulphur and oxygen pressure, having a value of 0.04.The Pt distribution ratio increased from 0.02 to 0.08 with temperature from 1340 to 1450 oC.For mattes where the proportions of Cu and Ni were kept constant, a slight decreasing trend was shown for the distribution ratio of Pt versus the iron content (37 to 53%) in the matte but was not confirmed because of experimental uncertainty."

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 Barbara Peszko, Tadeusz Tumidajski

"Various methods are used to identify the grain composition of fine-grained materials because so far the best notion of the grain size has not found and there is no single method to define grain size. In practice the most important are the following grain sizes: sieve diameter dt, effective diameter de, substitute diameter d2 and statistical diameter dst. The mentioned sizes are connected with the methods of analyses. Methods are correct but measure of different diameters of grain and their results are different.The most important methods of granulometric composition analyses are the following: the sieve analysis, the sedimentation method and the conductometric (Coulter-Counter) methods. In each of these methods various physical features connected with the grain size are measured.Sizes of grains defined by different formulas or measurement methods are associated mutually by dependencies, which are results of differences in their determination or calculation ways.In order to determine principles of results comparison the classification analysis results on linearly or non-linearly connected was made. Analyses which results demonstrate the same type of grain size distribution are treated as linearly connected. It is based on the general formulae which determines the probability density function of random variable which is the function of another random variable having the known density function.In order to show the difference in the grain composition of the same material qualified by different methods, three methods of investigations were distinguished. They are: the sieve analysis performed on precise sieves, the sedimentation analysis performed by means of a sedimentation balance “Sartorius” and the microscopic analysis performed after preparing a microscopic slide where the grain size was measured by the Martin’s method.The materials selected for the analysis were quartzite and glass, which are the material of high purity.The obtained results of mentioned above three types of analyses were approximated by distribution function of four distributions: Weibull, log-normal, cut Weibull and Gaudin-Schuhman."

Jan 1, 2003

By Steven Wright, Sharif Jahanshahi, Shouyi Sun

"While there is a large industry based on recovering platinum group metals (PGM) from complex sulphide ores containing Cu and Ni, there is little information on the thermodynamics of the matte phase formed on smelting the ore and in particular the behaviour of Pt in the matte.The equilibrium between metallic platinum and industrial mattes was studied in a series of experiments where a small quantity of matte (5g) and platinum foil of 150 µm thickness (0.5 g) were equilibrated in magnesia crucibles at 1400°C under conditions where the oxygen and sulphur partial pressures were controlled.The chemistries of the phases were determined from EDS analysis using a scanning electron microscope. Line scans were initially used to confirm that the foils had attained a uniform composition across their thickness. The composition of the matte was determined from analysis of an area of matte including the small metallic droplets and dendrites.The distribution of Pt in Cu-Fe-Ni mattes (Pt: 1.5 – 3%) and solid Pt alloys (Pt: 54 – 72%) was studied. For a matte of base composition 45%Fe, 11%Ni, 8% Cu, at a base temperature 1400°C, the following behaviour was observed for the Pt distribution ratio:Under the range of sulphur and oxygen pressure of this study (log pO2 from -15 to –12.2, log pS2 from – 4.6 to –2.2), the distribution ratio of Pt between matte and alloy was independent of the sulphur and oxygen pressure, having a value of 0.04.The Pt distribution ratio increased from 0.02 to 0.08 with temperature from 1340 to 1450 oC.For mattes where the proportions of Cu and Ni were kept constant, a slight decreasing trend was shown for the distribution ratio of Pt versus the iron content (37 to 53%) in the matte but was not confirmed because of experimental uncertainty."

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 Gideon Chitombo

"Mining is a "continuous" process of dependent breakage and materials handling stages, from the initial breakage of the in-situ rock, extraction from the pit or underground, and finally to the surface stockpile and downstream processing. Over time, underground and in-pit mining activities diverged into two separate disciplines, each using a variety of in-situ breakage techniques and surface activities, with processing techniques dependent on mineralogy or grades. This artificial separation of underground and open pit activities was exacerbated when the two became increasingly managed as separate cost centres rather than as an integrated unit. Mass mining essentially began in 1903 when metallurgist Daniel Jackling initiated the world’s first open pit, mining system at the Bingham Canyon porphyry copper deposit in Utah. The term mass mining has since been construed to mean large open pits and cave mining methods, including their variants. These methods are largely non-selective, involving the mass extraction of a deposit irrespective of the uneven distribution of grade and mineralogy. The advantages of mass mining have historically applied mostly to low grade, large scale deposits. With the depletion of mineral reserves closer to the surface, however, new deposits are deeper, lower grade and mixed with more impurities. These and other factors make extraction more difficult and costly. Mass mining is moving rapidly into a new and less certain environment where revolutionary changes are required to effectively deal with future challenges which are technical, economic and environmental (licence to operate). This keynote address presents current initiatives being considered for the next generation of both underground and surface mass mining systems in order to significantly reduce lead times and mining costs (CAPEX and OPEX), substantially increase productivity and meet license to operate requirements. The address is designed to solicit discussion on how better integration of mining and processing can become a platform for these next generation of mass mining systems and can also help the industry deal with the future challenges."

Jan 1, 2014

By Stephen Simukanga, Jewette Masinja

"Mining has been going on commercially in Zambia for over 100 years. The backbone of the mining industry has been copper production and its by-products of cobalt and gold. Over these years, the mining industry ownership structure has swung from private ownership to state ownership in 1972, and back to private ownership in 1995. Environmental management was first introduced into the body of Zambian legislation in 1991 through the promulgation of the Environmental Protection and Pollution Control Act (EPPCA). The Act’s main functions included the protection of the environment and control of pollution, and in particular to provide for the health and welfare of the people, animals, plants and the environment in general. This Act, was replaced in 2011 by the Environmental Management Act (EMA). The new Act has a number of new elements including: mainstreaming environment in national planning, it provides for the domestication of multilateral environmental agreements, enhances public participation issue, creates a central environmental information depositary, elaborates access to information principles, establishes an environment fund, creates enforcement orders, provides for both Zambia Environmental Management Authority and members of the public to sue for damages following environmental pollution, and provides for the appointment of honorary Inspectors. In addition to this, the Mines and Minerals Act of 1995 provided, for the first time, a section on environmental management in the mining sector. This section also created the Environmental Protection Fund (for mining), and made it obligatory to undertake environmental impact assessment before mining permits could be issued. The Environmental Protection Fund has now been established, as provided for by the law, and currently has more than USD9.0 million in the account. Secondly, environmental auditing is now being carried out annually on mines around the country, the effect of this has been a significant improvement in the environmental management of mining in Zambia. This paper looks at the response of the Zambian mining sector to these pieces of environmental management legislation, and the direction that the mining sector is expected to take on environmental management going forward."

Jan 1, 2014

By Ramon V. V de Araújo, Roberto B. E Trindade, Pablo R. Fica-Piras

"Lead has been reported to affect blood vessels and kidneys. It also produces adverse effects in the mental and physical development of children and nervous system of adults. It is also considered as a possible cause of cancer. Because of all these threats to the human life, the reduction of its environmental occurrence, by means of recycling, is an important additional advantage to the usual ones derived of the procedures of the secondary metallurgy: lead can be recycled several times maintaining its characteristics equivalent to the primary one.Furthermore, this way of producing the metal avoids the environmental impacts of primary lead melting. Also, as an additional advantage, it triggers the metallurgical process with a raw material in what we observe higher lead content than in the natural ores. Some of the potential sources for these purposes are: ashes, slags, electrode residues, anodic muds, spent electrolytes, solid and liquid wastes, industrial or automotive catalysts, worn-out or obsolete equipment components and/or final consumption products.About 40% of world’s lead production comes from automotive batteries, mainly composed of four parts: plastic box, electrolyte (diluted sulphuric acid), contacts and connectors of Pd-Sb and plates (PbSO4, PbO2 and PbO). The plates represent 75% of the total mass. Metallic parts can be melted at moderate temperatures and then refined. The remaining fraction, constituted by the non-metallic portions, can be recovered by hydro and electro-metallurgical routes. These routes are preferred instead of pyrometallurgical ones due to the ultimate emissions of lead particulates and sulphur dioxide.The principal constituent of the residual paste of batteries is the lead sulphate. In this process, the paste is treated in two stages: in the first, lixiviating with Na2CO3 (desulphurization of the paste), obtaining PbCO3 and Na2SO4; in the second, the lead carbonate is lixiviated with HNO3, producing Pb(NO3)2, soluble, that can be converted to metallic lead by electrolysis. The reaction of PbSO4 with Na2CO3 in aqueous solutions is fast: the global rate is limited by the diffusion of the carbonate ions inside the reaction medium."

Jan 1, 2003

"The thiosulfate leaching process developed by Barrick to treat sulfidic high preg-robbing gold ores uses calcium thiosulfate as the leaching reagent for ores pre-treated by pressure oxidation, resin for gold recovery with sulfite/trithionate elution and reverse osmosis as a means of reagent recovery. A large portion of the research that led to the development of the technology was based on previous studies completed by different groups over the years, mainly focused on the ammonium thiosulfate system. Operational limitations in the use of the ammonia-containing recycled water in the pressure oxidation circuit were some of the main drivers for the change from ammonium to calcium thiosulfate for the development of the industrial scale process. One of the main aspects for successful gold extraction and recovery in the thiosulfate system is the pseudo-equilibrium reactions that drive distribution of the different gold species (in solids, solution and on resin) in the system. Previous studies have been focused on the thiosulfate reactions and equilibrium constants for the oxysulfur ions (thiosulfate, trithionate, tetrathionate). However, the literature around the effects of the different metal-oxysulfur complexes (Cu and Hg complexes) that form when the ore is in contact with the leaching reagents, and the related effects on stability of the gold complex is limited. The main changes in the gold complex chemistry and stability in the calcium thiosulfate system as compared to the ammonium and sodium equivalents, as well as related effects on gold recoveries, were investigated in the presence of different types of double refractory ores. INTRODUCTION Barrick has developed a thiosulfate leaching process to treat double refractory gold ores, by combining the use of acidic and alkaline autoclave pre-treatment with thiosulfate resin-in-leach (RIL). The process currently in operation at the Goldstrike mine (the TCM process), uses calcium thiosulfate as the leaching reagent, resin for gold recovery with sulfite/trithionate elution and reverse osmosis as a mean of reagent recycle. The main feed to the process plant is highly preg-robbing sulfidic ore from Goldstrike’s open pit. Prior to feeding the pressure oxidation circuit, the ore is processed through the crushing and grinding circuits and treated in preparation for acid or alkaline autoclave processing (POX)."

Jan 1, 2018

By N. ??dyanik, Z. Kugukaldinova, O. Mishurina, Y. Glazkova, E. Mullina

"This paper describes the process flow of a selective processing method for acidic mine waters formed in the copper sulfide industry and characterized by a high content of copper, iron, and manganese ions. The proposed method comprises a series of sequential processes: the 1st stage is the recovery of Cu2+ ions by precipitation, the 2nd stage is the recovery of Fe2+ and Fe3+ ions as a dispersed phase by acid-base precipitation, followed by recovery in the 3rd stage of Mn2+ ions by converting Mn2+ with an oxidizing agent into insoluble forms of manganese and subsequent recovery of the dispersed phase by electroflotation. The developed method was tested on the acidic tailing storage facility (TSF) water of a mining project in the Urals region. The practical results of the implementation of the developed method have shown that its implementation will allow to recover copper, iron, and manganese in the form of salable products with a simultaneous decrease in their concentrations in adjacent water bodies down to the applicable MPCs. The process is a simple one, does not require any sophisticated expensive equipment and can be implemented either as a standalone solution or as part of existing treatment facilities. INTRODUCTION As a result of unsustainable utilization of natural resources in Russia, only a small fraction is processed into commodity products, while the rest is systematically dumped as emissions, effluents, and other wastes, polluting the environment. By amount of waste and concentration of valuable components, those wastes can be classified as aqueous technogenic resources [1, 2]. Therefore, the development of processing methods for this mineral resource category is an urgent and priority task that will significantly improve the industry’s profitability and the environmental conditions in the respective regions. MATERIALS AND METHODS Following research methods were mainly applied in this study: lab-scale and pilot-scale tests in a diaphragmless two-chamber electric flotation cell; for solutions and recoverable process products — chemical analysis using photometric determination techniques for metal cations and atomic adsorption determination techniques for the processing products. The phase composition of the precipitates formed in the process was investigated by X-ray phase analysis in the general-purpose diffractometer with a copper anode DRON-1."

Jan 1, 2018

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 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 Alan Bax, John D. Lewins

"Platinum Australia Limited (“PLA”) is currently undertaking a Feasibility Study into the development of the Panton Platinum Palladium Project located in the Kimberley region of Western Australia. The Panton Intrusive is a layered, differentiated mafic to ultramafic structurally complex body that has undergone numerous folding and faulting events. This has resulted in a southwesterly plunging synclinal structure some 10 kilometres in length and 3 kilometres wide.High grade PGM mineralisation is hosted within a number of stratiform chromitite reefs within the ultramafic sequence. The focus of the Feasibility Study is on the Top Reef which is situated approximately 150 metres below the mafic/ultramafic interface. The average true width of this reef is approximately 1.2 metres and the reef has a defined resource is 10.1 million tonnes at an average grade of 6.1 g/t PGM + Au.The Palladium to Platinum ratio of the Top Reef is approximately 1.15:1 and the reef also contains an average of 0.4 g/t Au and 0.3 g/t other PGM’s. The Panton ore is considered refractory in nature and standard flotation techniques achieve a PGM + Au recovery of less than 65% with a concentrate grade of less than 100 g/t PGM + Au. As part of the Feasibility Study Platinum Australia in conjunction with their major shareholder Lonmin Plc developed a new metallurgical process which has achieved an overall PGM + Au recovery of approximately 80% into a high grade PGM concentrate which is suitable for feeding direct to a PGM refinery.THE PANTON PROCESSThe Panton Process incorporates a two-stage Milling and Flotation circuit with no cleaning stages to produce a low grade, high recovery flotation concentrate. Typically the concentrate mass constitutes 25% of the feed and has a PGM + Au grade of 25 g/t.This low-grade concentrate is subjected to calcination in a rotary kiln or fluid bed at a temperature of approximately 400 0C for a period of 60 minutes. This step is designed to render the platinum minerals soluble in cyanide and both the temperature and the duration of calcination are critical to the efficiency of the leaching process."

Jan 1, 2003

By Bertil I. Pålsson, Sture V. Persson, Kent T. Tano

"Autogenous (AG) and semi-autogenous (SAG) mills often operate in an unstable state because of the difficulty to balance the rate of replenishment of large ore particles from the feed with the consumption in the charge. This has led to an increased interest in obtaining an accurate and direct measurement of mill load and the behaviour of the mill charge. A problem in attempting to measure those parameters is getting a sensor that is both robust and sensitive enough for continuous on-line measurement.Techniques that measure the force acting on the lifter when it hits the charge inside the mill have got an increased interest recently because of the ability to combine it with DEM modeling. This paper presents a method for the measurement of the apparent filling level in a pilot ball mill equipped with the Metso Continuous Charge Measurement system (CCM). In this technique a strain gauge sensor is mounted on a flat steel spring which is fitted into a recess underneath a lifter bar. In addition, a conductivity probe, the Boliden Grinding Measurement System (GMS), is mounted in another lifter bar with the purpose of comparing the two measurements. To visualise the behaviour of the charge a 2D DEM modelling technique is used with Metso HFS software.The pilot mill is a grate-discharge mill, equipped with 12 rubber lifters of square size 0.1 m, face angle 45 degrees. Steel balls in the size range 10-30 mm and density 8000 kg/m3, are used in the experiments. Test material is a hematite pellet feed, d50 around 45um, chosen to get stable grinding conditions with respect to feed size variations.The experiment is meant as a first test of the equipment’s performance, and to study how the sensors respond to changes in some operating variables. To get an understanding of, and distinguish between correlation and causality, experiments are performed according to a full factorial design with two levels, and in addition two replicates of the experiments at a center-point in the charge level setting."

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

By Jean-Paul Franzidis, Robert G. Coleman, Emmy V. Manlapig

"The Floatability Characterisation Test Rig (FCTR) is a self-contained, highly instrumented mobile pilot flotation plant developed by the Julius Kruttschnitt Mineral Research Centre, the Mineral Processing Research Unit of the University of Cape Town and EIMCO, as part of the Australian Minerals Industries Research Association (AMIRA) P9 Project. Apart from being a fully operational pilot plant, the FCTR was designed to determine flotation model parameters and to develop and validate flotation plant modelling, scale-up and simulation methodologies.The FCTR was installed at WMC’s Kambalda Nickel Operation where circuit modelling, simulation and scale-up test work was performed using the AMIRA P9 flotation model as the basis of the analysis. The model parameters were obtained through metallurgical sampling, batch flotation tests and gas dispersion characterisation around the FCTR. Model parameters were determined for four FCTR circuits, each of increasing complexity. The circuits ranged from a simple rougher-cleaner configuration with no recycle streams, to a more complex rougher-cleaner-recleaner configuration with two recycle streams.Using the P9 modelling methodology, the system was analysed using four mineral species: nickel sulphide, iron sulphide, copper sulphide and non-sulphide gangue. The floatability of each mineral was analysed as two floating species (fast and slow) and a non-floating species. Mass balanced data from all four FCTR circuits were regressed simultaneously together with data from 47 batch flotation tests. Nonlinear regression was used to determine the solution. The model fit was found to be accurate with most data points predicted within experimental standard deviations. A Monte Carlo sensitivity analysis was also performed to establish the stability of the regressed parameters.Using the P9 simulation methodology, simulations of five FCTR circuits (different from the previous four) were performed. The FCTR was also operated in these five circuit configurations to obtain experimental data to validate the simulated predictions. The simulations were found to predict the recovery and grade of nickel sulphide and copper sulphide within experimental standard deviations. The prediction of recovery and grade of iron sulphide and non-sulphide gangue was less accurate. Overall the FCTR simulations predicted the changes in circuit configuration well."

Jan 1, 2003

By S. K. Kawatra, T. C. Eisele

"Coal-fired electrical power generation plants produce 56% of all the electricity in the U. S., burning approximately 860 million tons of coal annually. This results in production of 58 million tons of fly ash; 19 million tons of bottom ash and boiler slag, and 23 million tons of desulfurization sludges. These are a considerable disposal problem, and it would therefore be very valuable to be able to sell these residues and byproducts as useful materials, rather than paying to dispose of them in landfills. However, utilization rates are currently very low, below 32% even for the most thoroughly commercialized combustion byproduct (fly-ash). This poor utilization rate is a result of the high impurity content of combustion byproducts, which make them unsuitable for existing markets. The experiments described in this paper were therefore carried out to study the application of mineral processing techniques to upgrading combustion byproducts.Experiments were conducted to upgrade and purify low-grade combustion products to produce highgrade, readily saleable materials. A process was developed for removing unburned carbon from coal fly-ash by froth flotation, using reagents originally developed for flotation of oxidized coals. This technique could reduce the carbon content of fly-ashes containing up to 11.1% carbon to less than 2%. The froth product was sufficiently carbon-rich that the recovered carbon has value as fuel, or as low-grade activated charcoal.Fly ash was also examined as a binder for producing iron ore pellets, primarily as a substitute for bentonite. It was found that Class F fly ash in combination with an activator (calcium hydroxide) was an effective pellet binder at dosages comparable to the currently-used dosages of bentonite clay. While the flyash worked very well alone, tests in combination with bentonite showed that fly-ash/bentonite mixtures had significantly worse binding performance than either pure bentonite or pure fly-ash-based binder. This was determined to be due to the fact that bentonite and fly ash have profoundly different binding mechanisms, with fly-ash undergoing a pozzolanic chemical reaction while bentonite binds through a physical attachment process."

Jan 1, 2003

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 I. Gombköto

To sustain the growth of industrial production necessitates the increasing of the amount of processed mined raw and secondary materials. As a side effect of raw material production, the amount of tailings material, - coming from mineral processing operations ? increases as well. Using wet technology, these tailing materials are generally transported and stored with the water used for previous operations. This habit could lead to dangerous situations. Enough to remember the disasters had happened to the last decade, safe tailings operations need to remove as much water from the solid as possible. Environmental, technical and economical needs should meet, therefore using a technology combining these specific needs could be necessary. Paste technology was introduced generally into tailings operations at the last ten years, as an answer to the call of the above mentioned challenges, however there are still many questions to answer within the frame of using it. The Institute of Raw Materials Processing and Environmental Process Engineering of the University of Miskolc has been dealing with mechanical process engineering, especially by the support of the EU project TAILSAFE Contract nº EVG1-CT-2002-0066 and the NKFP 3A/068/2004 Hungarian fund extensive research has been carried out about paste technology. Different test methods and materials were applied. Tested tailings materials were as follows: different fly ashes from coal power plants from Pécs ? Hungary, Gyöngyös ? Hungary, Neyvil ? India, different Croatian ashes, hazardous waste incineration plant ashes from Dorog ? Hungary, different kind of sands from Hungary, fine glass sand from Fehérvárcsúrgó ? Hungary, flotation ore processing tailing from Gyöngyösoroszi ? Hungary. Different additives, as gypsum, bentonite and cement were tested as well. The applied test methods were as follows: physical material testing (laser sizer, piknometer, different microscopes), X-ray diffraction analysis, settling columns, the three measuring pipes tube viscometer (16~27 mm pipe diameter), a hydraulic test loop with different pumps (40~53 mm pipe diameter, 0.2~4 m/s average slurry velocity range, 0%~52 % volumetric concentration range), rotational viscometer, Cassagrande yield locus tester and the slump cone test. This paper summarizes and systematizes the results of the aforementioned research as well as reports about the developed paste pipe transport design method based on the fine suspension ? coarse mixture model. The paper also reports about a systematic experimental series with different materials to establish criteria when high concentration suspensions behave like paste.

Jan 1, 2014