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By Carin Laubscher, Francis W. Petersen, Jaap P. Smit

Waste streams, such as acid mine drainage, are often characterised by low pH values and high concentrations of heavy metals, dissolved solids, calcium and sulphates. Although lime remediation effectively removes most of the heavy metals as hydroxides, it is less effective at lowering levels of sulphates. Various methods of removing sulphates from effluents exist, such as precipitation with lime, precipitation with barium salts, co-precipitation with calcium carbonate, reverse osmosis, and ion exchange. Mintek developed a chemical precipitation (SAVMIN) process to treat acid mine drainage, which entails the addition of lime to precipitate the metal hydroxides, and the subsequent formation (precipitation) of calcium sulphoaluminate or ettringite. The key to the viability of the new technology lies in the correct use, regeneration and recycling of Al(OH)3 used to precipitate the ettringite. The water produced by this process is suitable for disposal to watercourses or for agricultural, domestic or industrial consumption. No brines are produced as the salts are converted to solid hydroxides, gypsum and calcium carbonate. The technology has been tested on several different waters in pilot plant campaigns. Results obtained indicate that potable water can be produced (containing less than 200 mg/L sulphate and no heavy metals) as long as the monavalent ions (Na+, Cl-, etc.) are within limits.

Jan 1, 2003

By I. H. Mukhametshin, E. N. Baranova, I. B. Fadina, E. A. Ashirbaeva

The purpose of the research is the development of a complex of solutions for the maximum extraction of non-ferrous and precious metals from persistent mineral raw materials by heap bioleaching from spent heap leaching (HL) stacks. Methodical recommendations for assessing the suitability of primary and technogenic refractory mineral raw materials for heap bioleaching are developed. Active associations of microorganisms have been created for the conversion from various types of ores to the solution of S, Fe, As, Sb, Cu, Zn, Mn, Ni, Mg, P and other elements, as well as methodologies for their storage, immobilization and preparation of bioreagents in industrial conditions. On a pilot scale, tests were carried out on samples weighing 15-17 thousand tons of refractory gold-sulphide ores (more than 50% of gold is associated with sphalerite), gold-quartz ores with colloidal gold (74% associated with quartz and pyrite) and gold-silver ores with elevated copper and zinc content (1.5 and 3,5%, respectively), as well as man-caused material lying for 4-5 years of spent quarry material of oxidized gold-silver ores. In the pilot-industrial tests of heap bioleaching of gold-sulfide ores, gold recovery of 84-85% and silver was achieved to 89-90%, the possibility of obtaining high-yield solutions of copper and zinc, suitable for hydrometallurgical processing, from gold-silver ores, and the possibility of obtaining waste with a dump content of valuable components, suitable for deep disposal in the construction industry. When comparing two technologies for processing refractory ores after biooxidation under HL conditions, when 1000 tons of ore processed by the bioreagent were re-milled from a size of 40 mm to 0.1 mm and cyanated under the conditions of the factory process, the same results were obtained for gold recovery (85%) and silver (90%), as with the heap version. The copyrights of the development are protected by a patent.

Jan 1, 2018

By Tasuma Suzuki

Electrokinetic/permeable reactive barrier system is a promising in situ soil and ground water remediation technique to reduce toxic NO3- into less toxic NH4+. Using granular zero-valent iron (Fe0) as a reductant, the first objective of this study was to investigate the influence of the solid-liquid ratio and aqueouspHon NO3- reduction. The results obtained from a series of batch experiments showed that NO3- reduction was enhanced by either increasing solid-liquid ratio or decreasing aqueous pH. Based on insights obtained from batch experiments, the second objective of this study was set to design the remediation conditions of the electrokinetic/Fe0permeable reactive barrier system to maximize the NO3- reduction efficiency. Experimental results showed that the effectiveness of the system strongly depended on the Fe0 percentage in the reactive barrier, the pH in the anode reservoir, and the applied voltage, which were consistent with the results obtained from batch experiments. Under optimized treatment conditions, nearly 100 % NO3-was reduced into NH4+ in the permeable reactive barrier and collected in the cathode reservoir. Insights obtained from this study provided fundamental information on roles each of remediation design parameters plays, and will be useful to optimize the remediation conditions. Keywords: electrokinetic remediation, permeable reactive barrier, zero-valent iron, nitrate

Sep 1, 2012

By Sunil Tripathy, Y. Rama, Srinivasulu. A., Amit Ranjan

Process improvements in an operating plant are always challenging. Mineral beneficiation plants based on gravity concentration techniques need continuous evaluation and monitoring of its processes for getting maximum recovery and better grades. But, in an operating plant it is very difficult to control all the parameters due to numerous reasons such as unsteady operation, fluctuation in the quality of run-off-mine ore, overall flow rate etc. For better understanding of the beneficiation circuit, it is necessary to evaluate the critical operating parameters which affect the performance in terms of grade, recovery and throughput including losses of valuable materials into tailing. Accurate data collection and proper data interpretation followed by making necessary change which is implementable in an operating plant play very critical role in performance of the circuit. In case of gravity operated beneficiation circuits of chrome ores where the quality of the feed and physical parameters varies continuously, the operators are required to modify the critical operating process parameters on continuous basis which is very difficult and tiresome. There are many causes of the data variability, including both error (sampling and assay), and real variation in performance due to changes in ore mineralogy, operating conditions and other factors. In this article, attempts made to evaluate the performance of ultra-fine beneficiation circuit in terms of silica reduction in the concentrate of chrome ore beneficiation plant (COB), India are discussed. The approach adopted and practical problems encountered during the study were also discussed. Results obtained from plant audit based on the above methodology has shown that SiO2 content in the concentrate can be reduced to <4%.

Jan 1, 2014

By Reuter M. A., R. D. van der Weijden, W. F. C. van Wageningen

"Copper(II) can be recovered or removed from acidic copper sulfate solutions as cuprite or metallic copper powder by reduction with carbohydrates. The copper powder characteristics, such as size and shape of particles, determine the tendency to adhere to reactor walls and to agglomerate. In order to make this process suitable for a commercial scale pipe reactor, process conditions and the reactor configuration were varied in order to influence the copper characteristics in a positive way. The aim was to achieve proper particle throughput in the pipe reactor and to obtain a well defined copper powder.In this paper the effect of both, chemical and physical parameters on the shape and size of particles were systematically studied in a number of autoclave experiments. These parameters include mixing, Cu(II) concentration, pH, temperature, seeding, use of additives and reactor materials. Additionally, Monte Carlo simulations of copper growth inside a Kenics static mixer were made. Results show that the use of additives and the use of static mixers influence particle characteristics the most."

Jan 1, 2003

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

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

Jan 1, 2003

By 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 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 Markus Dammers, Christopher Robben, Hermann Wotruba, Christian Schropp

"In most underground mining processes the entire extracted ore is transported from underground workings to surface processing plants for separation of valuable minerals and gangue material. Most of the transported material consists of barren rock with negligible metal content, especially for low grade deposits, such as in the copper or gold metal ore mining. Increasing mining depths result in higher costs for transportation and hoisting. Therefore, rejecting waste rock as soon as possible from the material stream gains importance. The concept of resource to product integration in the form of earliest waste rejection in combination with subsequent backfilling follows the philosophy of ‚leaving waste underground?. Implementing mineral processing underground can lead to less required mass movement to surface, hence reducing transportation and hoisting costs. At the same time, rejected waste can be used as backfill to increase extraction rates by reducing pillar volumes. In the mill, a stable high grade feed leads to decreased specific operating and investment costs as well as increased productivity and recovery. These effects as a whole have a large potential to reduce cut-off grades so that resources can be turned into reserves. Within the I²Mine (Innovative Technologies and Concepts for the Intelligent Deep Mine of the Future) project of the European FP7, investigations are carried out by the Unit of Mineral Processing of RWTH Aachen University, the Institute of Mining Engineering I and TOMRA Sorting Solutions | Mining. One aim of the cooperation is to develop new concepts for a comprehensive integration of near-to-face processing in combination with backfill into the overall underground mining process. Effects on up-, down- and side-streams are investigated to prove the potential of resource to product integration in comparison to common underground mining systems and processing methods."

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 Rebecca Hope, Derick Moolman, Frikkie Malan

"Despite the lip service that has been paid to pro-active plant maintenance processes over recent years, a significant portion of maintenance in industry is still reactive. The business driving force to prevent expensive production opportunity costs arising from “break-down maintenance” is obvious. Various benefits can be derived from successfully deploying remote equipment diagnosis technology and associated business processes.From an end-client’s viewpoint these include the ability to predict and take actions to prevent equipment breakdowns, increasing the lifetime of equipment by responding to appropriate operating instructions and therefore improving the return on capital expenditure. Better planning and scheduling of maintenance priorities and resources with performance measures like an Equipment Health Index are also possible. The knowledge that a qualified supplier engineer is constantly in touch with the operating conditions of their equipment, albeit remotely, is more than a comfort, and can be translated into quantifiable cost savings and improved supplier service levels.This paper analyses the reasons for the inadequate level of pro-active plant maintenance practice in industry today, and presents a number of important criteria in selecting appropriate solutions to this problem. A case study of a specific real-time, remote equipment management application is presented."

Jan 1, 2003

By Rakesh Kumar, S. Mehrotra, T. Alex

"This paper, an overview of our recent findings on mechanical activation (MA) of minerals/materials, emphasizes the importance of sample genesis, mechanically induced/altered porosity and surface area, mineral interactions, glassy inorganic materials, surface alteration and zeta potential changes and, mechanically induced reactivity of solids. Materials investigated include Al-oxyhydroxides (gibbsite and boehmite), fly ash and granulated blast furnace slag. Planetary, attrition, vibratory and conventional ball mills are used for MA. Genesis of boehmite has been found to have a bearing on its behavior during MA. For example, BET specific surface area (SSA) of boehmite prepared by thermal dehydroxylation of gibbsite has decreased from 265 to 65 m2/g during 240 min of MA; in contrast, the SSA of hydrothermal boehmite has increased from ~2 to 36 m2/g. Mechanisms of surface area changes in the two boehmite samples differing in their genesis is explored. MA of gibbsite and its mixture with hematite/quartz using attrition milling has indicated that the presence of the second phase promotes amorphisation. Amorphous materials show signs of change in nature of bonding during milling as illustrated by MA of fly ash. Physicochemical changes during MA are not restricted to the bulk phase. The genesis of zeta potential changes in MA solids can be many; for example texture induced zeta potential changes as observed for gibbsite, while zeta potential changes during the milling of granulated blast furnace slag occur due to enhanced (possibly non-congruent) dissolution. Interesting manifestations of mechanically induced reactivity and its correlation with physicochemical changes are illustrated in terms of alkali leaching of boehmite and, hydration of MA slag. New findings reported here are associated with several open questions and are highlighted in the paper."

Jan 1, 2014

By T. Ueda, T. Oki, S. Koyanaka

"Accurate assessment of the liberation state of crushed ore particles is important for efficient mineral processing. In general, the liberation state is assessed by two-dimensional (2D) measurement of polished ore sample sections. However, this 2D measurement inevitably suffers from overestimation of the degree of liberation, known as stereological bias. This arises from the fact that biphase particle sections of which only one phase happens to have been cut are indistinguishable from liberated particles. To date, several stereological correction methods have been proposed, but their applicability for various types of particles has not yet been sufficiently examined, and this tends to undermine their practicality. We have addressed this problem using a numerical-analytical approach in which various types of biphase particles are modeled, and the 2D sectional information is compared with actual three-dimensional (3D) information. Through simulations, we revealed a general relationship between the internal mineral structure of particles and the stereological bias. Finally, we have developed a unique stereological correction method in which the texture (a 2D pattern characteristic) of particle sections is used to estimate the internal structure of particles, and thereby the stereological bias. KEYWORDS Mineral liberation, stereological bias, texture analysis INTRODUCTION Mineral liberation assessment of 2D particle sections inevitably suffers from stereological bias; that is, overestimation of the degree of liberation. Stereological bias is caused by the fact that a composite particle can be misidentified as a liberated particle when only one phase happens to have been cut in sectional measurement. Stereological bias has attracted attention since Gaudin pointed out its importance in 1939 (Gaudin, 1939). Several attempts have been made to measure the 3D liberation state directly, avoiding the bias, using X-ray computed tomography (Gay and Morrison, 2006; Lin and Miller, 1996; Miller et al., 2003; Miller et al., 2009; Reyes et al., 2017; Videla et al., 2007). These have provided useful information through laboratory testing, but further technical refinement is necessary for practical usage, to overcome the technique’s limitations in terms of resolution, assessment of minerals of similar density, and speed. Therefore, for practical purposes, detailed information regarding mineral phase geometry is obtained by sectional analysis, using automated scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDX)-based analysis (e.g., with a mineral liberation analyzer (MLA) (Fandrich et al., 2007; Sandmann, 2015)); and the development of an effective method of stereological correction, which predicts the relevant bias and transforms the measurable 2D degree of liberation into its 3D counterpart, is an important research aim."

Jan 1, 2018

By Xin Tan, Changgen Li

"The floatabiliby of chelate CF-collector for zinc and lead oxide minerals was described. It found that CF-collector possesses a strong collection power for zinc and lead oxide minerals as well as excellent selectivity for the gangue minerals. A new technology of zinc and lead oxide flotation with CF reagent as a collector, lead nitrite as a activator and water glass as modifier was presented. The mechanism of interaction between reagents and minerals was discussed by means of adsorption, zeta potential, nephelometric titration, XPS and infrared spectra was investigated.CF-collector, newly developed by Beijing General Research Institute of Mining and Metallurgy (BGRIMM), is a kind of chelate collector for the flotation of oxide minerals. CF-collector mainly consists of N-nitroso-N-phenylhydroxylamine ammonium salt. The CF-collector was used for the selective flotation of scheelite in the Chinese plants.In this paper, the effects of the dosages of activator Pb(NO3)2 and depressants (sodium hexametaphosphate, polyphosphate, water glass and salified water glass) on the floatabilities of several minerals (cerussite, smithsonite, calcite, dolomite, limonite and quartz) as well as their mixtures were investigated in the presence of the CF-collector. The results show that the CF-collector is the excellent collector for selective flotation of cerussite and smithsonite. Pb(NO3)2 can selectively activate the oxides of lead and zinc resulting in a decrease of the CF-collector dosage. The sodium hexametaphosphate plus the salified water glass are the effective depressants for gangue minerals. Based on the above facts, the “CF process”, namely, used CF reagent as a collector, Pb (NO3) 2 as a activator, and sodium hexametaphosphate plus salified water glass as depressant, has been used for the flotation separation of the lead oxide mixtures or zinc oxide mixtures without disliking and heating. For the feed lead assaying 19.07%, the lead concentrate assaying 49.81% Pb at the recovery 80.69% was obtained after one step flotation. For the feed zinc assaying 12.85%, a zinc concentrate of assaying 29.56% Zn at recovery 83.87% was obtained."

Jan 1, 2003

By G. A. Wierink

This paper discusses a new method to increase flotation recovery. As known from literature, fine and coarse particles have different flotation rate constants, hydrodynamic behaviour and require different reagent regimes. The device discussed allows separate processing of finer and coarser slurry by extraction of a third stream, carrying finer slurry, from the flotation cell. By separate treatment of fine and coarse slurry operational conditions and so flotation recovery for both may be optimized more efficiently. Extraction and classification of the third stream is accomplished by low speed centrifugation and Taylor-Couette flow separation. This Dual Outlet Device (DOD) can be installed in a traditional flotation cell without need for equipment replacement. In order to asses different design options for the DOD a transparent laboratory scale model was built. For this scale model Computational Fluid Dynamics (CFD) simulations using the RANS k-e and LES turbulence models were performed. Essential insight in the dominant flow systems relevant to optimal operation of the DOD was obtained from the CFD simulations and flow visualization tests with the laboratory scale model. Based on these findings a number of configurations were investigated at pilot plant scale in a 5 m3 Outokumpu flotation cell. The results of the pilot plant study show that utilization of the DOD provides a method for in-cell control over particle size distribution in the slurry. Use of the DOD in a flotation cell may enhance flotation recovery and decrease flotation reagent consumption significantly, against marginal investment and operation costs.

Jan 1, 2014

By Y. Nahmad- Molinari

We present a novel on line inductive sensor for the determination of the quality of the concentrates of iron ores. This device is coupled with a cheap USB Data Acquisition System that makes it versatile enough to simultaneously control up to seven fluxes at a very low cost (< $300 US dollars), and achieves a resolution better than 0.5 % on the determination of the magnetic iron content in the concentrate. A RLC circuit with its inductive element placed surrounding a sample of pure magnetite concentrate is tuned at its resonance frequency, by means of adjusting, the feeding voltage of a voltage-controlled oscillator (VCO) and several samples with mixtures of different contents of silica and magnetite are placed in order to get a calibration curve. After some signal conditioning, a National Instruments USB-DAQ NI-6008, acquires the amplitude of the signal via USB port on a PC using a Lab-View program designed for such purpose, in which the calibration curve is used for on-screen data presentation directly in percent of magnetite content. The implementation of this device for control purposes on line directly placed on the concentrators would allow better efficiency of the process and higher quality of the final concentrate by con-trolling; the rotation speed, the rising or dilution water fluxes or bypasses towards milling recirculation cycles.

Jan 1, 2014

By A. J. Lynch, L. Ergun, M. Oner

"A research program on modelling cement grinding circuits has been in operation at Hacettepe University, Ankara, for four years. It has concentrated so far on tube mill and air separator grinding circuits for cement clinker, with emphasis on plant sampling surveys, including axial sampling inside the tube mills. The methodology is to use plant data to build the models and to supplement this by laboratory data where necessary, for example the determination of breakage functions. The plant data come from comprehensive sampling surveys and so far 33 surveys of clinker grinding circuits have been carried out in 9 plants. The operating conditions have been• mill sizes – 3.2 to 4.8 metres diameter and 8.5 to 15 metres long,• mill feed rates – 46 to 158 tonnes per hour,• air flow through mills – 25000 to 125000 cubic metres per hour,• cement clinker work indexes – 10.3 to 18,• separator sizes – 2. to 3.1 metres diameter,• separator feed rates – 132 to 689 tonnes per hour,• separator speeds – 12.3 to 21 metres per second.The ball mill model is Whiten’s perfect mixing model and the separator model is the Tromp curve with a fish-hook. This paper emphasises on the importance of calculating the breakage rates and the discharge functions with three case studies at five different circuits which were selected for discussion because they show how particular features of circuit operation can be included in the general models. Size distributiongraphs are used to illustrate every aspect of the discussion.In case I the special emphasis on calculating the breakage rates and discharge rates separately is given in a high pressure grinding roll-ball mill-separator circuit. The tonnes of each size fraction in the mill and the calculated values of R/D, D and R are determined. The values of R per mw are also given to allow comparison with mills of other sizes. The circuit allows the comparison of the static type (V Sep) and dynamic type separators (SKS). Comparing the reduced efficiencies shows that the dynamic separator is slightly more efficient than the static one.In case 2 data are given from two compartment tube mills having the same diameter and the motor power but different ball size gradation. The breakage rate particle size variation of the second chamber of two mills indicate that having finer ball size distribution causes higher breakage rate values."

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 Tim Suljada, Mary Stewart, Jim G. Petrie, Damien Giurco

"The minerals industry is being challenged to reduce the amount of virgin ore that is mined, and to replace this material through the recycling of used commodity items and scrap, or by the reprocessing of waste materials. It is argued here that the existing technology base of minerals processing and refining offers real potential for handling these secondary resources. The challenge is to develop tools by which the most preferable recycling routes (both economically and environmentally) can be identified from a list of feasible alternatives, taking into account any operational constraints of these technologies.This paper describes an heuristic approach to developing the family of all technically feasible flowsheets to address this challenge, from which a preferred option may be selected according to a set of decision criteria (economic and environmental). Our approach uses conventional flowsheeting techniques of selecting flow variables and splitter functions, supported by design performance information for each unit operation. This set of design decision variables is augmented by knowledge of the suitability of a particular waste or scrap stream for a given unit operation within a flowsheet. We achieve this by comparing the composition of the scrap stream with the range of mineral streams for which the unit operation was designed initially. This is inspired by the “overlap” approach proposed by Legarth, where an “overlap” of 1 would suggest that there is high degree of compatibility between a given secondary resource stream and a primary mineral stream as inputs to a specific technology. The “overlap” concept has been extended to include information about the physical characteristics of secondary resource streams, as well as information relating to synergistic / antagonistic influences of minor elements present in the waste stream. A flowsheet which delivers a product of acceptable quality from a given secondary resource material is built up from a progression of unit technologies. The exercise is repeated to generate the family of all feasible flowsheets from combinations of acceptable unit technologies."

Jan 1, 2003

By Kaioeng Wang, Qi Liu, Yahui Xiang

"In the differential metal sulfide ore flotation it is desirable to replace the toxic inorganic depressants with environmentally benign chemicals. Chitosan, as a natural and non-toxic polymer, has been proven to be an efficient depressant for chalcopyrite while allowing galena to be floated by xanthate collectors. However, the poor solubility of chitosan limits its potential applications as the flotation could only be carried out at about pH 4 where chitosan is soluble. A carboxymethyl derivative of chitosan, named N-carboxymethyl chitosan (N-CMC), was synthesized by substituting the amino groups of chitosan with carboxymethyl groups. The substitution significantly improved the solubility of chitosan. The structure of N-CMC was studied and compared with chitosan via Fourier transform infrared spectroscopy (FTIR). Flotation tests were performed on single minerals and mineral mixtures (with weight ratio of 1:1) with the addition of appropriate amount of potassium ethyl xanthate (KEX) and N-CMC. The solution pH was varied from neutral to alkaline. The flotation concentrates and tailings were collected and analysed for the contents of copper and lead. FTIR measurements showed that new peaks of C=O stretching of -COOH and N-H deformation of -NH- appeared in N-CMC, which indicated that the carboxymethyl groups were introduced and the amino groups were the sites for the substitution. Flotation results indicated that N-CMC could depress either chalcopyrite or galena depending on the pH. The results were not affected by the sequence of KEX and N-CMC addition. Therefore, N-CMC is potentially useful in Cu-Pb sulfide separation following a bulk Cu-Pb flotation. The N-CMC was also found to have surface cleaning functions, and was able to remove contaminating copper ions from galena surfaces. Therefore, its application in sulfide ore flotation is expected to be more robust than the original chitosan."

Jan 1, 2014