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By T. S. Reddy

Research and Development Centre for Iron and Steel (RDCIS) a unit of Steel Authority of India Limited (SAIL) is continuously engaged in reduction of energy consumption at SAIL plants by implementing innovative and new concepts. In this regard, continuous efforts are being made to recover waste heat in Sinter Plants. This paper discusses existing waste heat recovery measures taken and proposed measures planned in Sinter Plants. One such effort is on waste heat recovery from sinter coolers. Hot sinter is discharged to the crusher at the end of the sinter machine at a temperature of 500 to 800°C. Temperature of hot sinter is brought down to nearly 100°C in the sinter cooler with air-cooling. The air after cooling the sinter is generally discharged to the atmosphere at about 225 to 300°C. It is planned to recover heat from the hot air that is being released to atmosphere and heat the process water, which is being added at ambient temperature in mixing drum at Bhilai Steel Plant. The temperature of raw sinter mix will be raised by addition of this hot water, which will help in improving the productivity of sinter machine. It is estimated that Waste heat recovery to the tune of 1.5 to 2.0 Gcal/h is possible with reduction in CO2 emissions in the range of 4000 to 5000 ton/year. The novel approach that is being adopted is addition of hot water in mixing drum for higher sinter productivity for the first time in India. Keywords: waste heat recovery, sinter plant, hot water generation, emission reduction, CDM

Sep 1, 2012

By A. Lewis

"Thiol collectors including the xanthates and dithiophosphates have dominated the sulfide mineral processing industry for over a century. Tecflote represents completely different chemistry, without sulfur or phosphorus, and will float all sulfides and associated precious metals. As these collectors are surfactant in nature, they comprise a head group which binds to mineral surfaces, a spacer and a long hydrophobic tail. The modification of the spacer behind the head group allows for collector optimisation for different sulfide ore types and process conditions.The Tecflote surfactants have been designed to be either very selective against pyrite at the natural pH of the ore (pH 7-9) or to float all sulfides including pyrite. Depending on the ore type and the process flow sheet, the use of lime can be maintained, reduced or completely eliminated.Tecflote can be used either as a rougher collector giving good recovery and grade for the sulfide minerals or it can be used to target valuable minerals after regrind and through cleaner flotation. It has repeatedly shown to be very effective at holding onto gold through the cleaner steps. The low solubility has a significant impact on the mechanism and surface activity of the collector, resulting in a very different flotation response compared to conventional thiol collectors.INTRODUCTIONXanthate was first made in 1882 by Zeise and first used in flotation in 1924 (Keller, 2018). In 1946 Keller patented thionocarbamate as a collector, which was produced by Dow Chemicals (Keller, 2018). Later it was replaced by Dow product Z-200, while dialkylthionocarbamate was discovered by Harris et al. (Harris, 1954. No significant chemistry change to collectors has occurred since they were introduced in the mid-20th century and now that the feed grades have been declining over the last decades creating a need to find more selective collectors to extract difficult and complex ores and pushing the industry to look at other reagents."

Jan 1, 2018

By Mingxia Liu, Qi Liu, Tao Jiang

"In addition to physical parameters such as small mass and high specific surface area of fine and ultrafine minerals, chemical parameters such as the adsorption affinity of collectors on the minerals also plays an important role in fine particle flotation. In this study, we have examined collectors with two different ionized groups, carboxylate and hydroxamate, on the flotation of fine niobium oxide (pyrochlore). To facilitate comparison, two hydrocarbon radicals were tested: octyl and oleoyl, which led to four collectors that were studied: octyl hydroxamic acid (OHA), sodium octanoate (C8OONa), oleoyl hydroxamic acid (C18HA), and sodium oleate (NaOl). Small-scale flotation and isothermal microcalorimetric titration measurements were performed to determine the flotation recoveries of different sized pyrochlore and the enthalpic behavior after adsorption of the collectors on pyrochlore. It was found that the flotation performance of the carboxylate-based collectors was generally inferior to hydroxamate-based collectors. Sodium octanoate could not float pyrochlore irrespective of the particle size of the pyrochlore tested. With a longer hydrocarbon chain, sodium oleate was effective to float the relatively coarse pyrochlore (>20 µm) but its collection efficiency dropped sharply for particles smaller than 20 µm. On the other hand, the two hydroxamate-based collectors, octyl hydroxamic acid and oleoyl hydroxamic acid, showed good collecting ability to both the coarse and fine pyrochlore. The isothermal microcalorimetric titration studies indicated a consistent correlation of chain length with floatability of collectors for relatively coarse pyrochlore, as well as a positive relationship between the adsorption affinity and fine pyrochlore flotation recoveries. The key finding of this study was that efficient fine particle flotation could be achieved when strongly chemisorbing collectors were used.INTRODUCTION The first detailed study of the effect of particle size on flotation was made by Gaudin (1931) with sulphide ores. In 1942, Gaudin again demonstrated that (Gaudin et al., 1942) fine particles possess different flotation properties from larger particles. Since then the effect of particle size on froth flotation has been an important research topic by many researchers, e.g., Gaudin (1957), Miettinen et al. (2010), Warren (1976) Jameson (2010), summarizing the behavior of fine particles in terms of their low particle momentum, leading to low rate of collision with bubbles which reduces the chance of adhesion. The suggested remediation methods are mainly based on two approaches: increasing particle size or decreasing bubble size (Warren, 1976). Sand-fine splitting followed by separate flotation treatment of the sand and fines, using deep flotation cells, using starvation quantities of collectors, and using long flotation times, are also strategies to address the problems of fine particle flotation."

Jan 1, 2018

By Dee Bradshaw

"Process mineralogy’ is a form of applied mineralogy which focuses on addressing problems associated with the processing of ores. ‘Mineralogy’ is the scientific study of minerals and ‘mineral processing’ is the production of concentrates from ores. ‘Process mineralogy,’ however can be defined as the practical study of minerals associated with the processing of ores, concentrates and smelter products for the development and optimisation of metallurgical flowsheets, including the waste and environmental management considerations. This hybrid discipline consists of teams that include geologists, mineralogists, samplers, mineral processors and often others, working together. The degree of cross-training, communication and trust dictates the potential capacity of the team and where an appropriate work dynamic is fostered, in which relationships flourish as much as does the ethic of technical excellence, it is possible to develop technical capabilities that surpass those of conventional teams. The world’s demand for metals is ever increasing and ore deposits available for extraction and processing are lower grade and more complex, often containing deleterious elements that require tailored treatment. Generally, in the past, the technical challenges only needed to be overcome and assessed economically to make an ore deposit viable; increasingly and in the future, a more sustainable approach including environmental and societal considerations is needed. Process mineralogical assessment is increasingly providing the critical information that stands between failure or collapse and survival or success of some mining operations. In this paper, selected case studies are used to demonstrate the valuable role of the process mineralogy tools being used to provide the platform for innovative technology development. Their common attributes are discussed and distilled, thus providing some insights and potential guidance for addressing some of the likely future challenges of the mining industry."

Jan 1, 2014

By Tohru Kamo, Shigeyuki Katano, Hideki Nakagome, Maiko Adachi, Shingo Nakamura, Kaneshi Taniguchi, Zar Zar Hlaing, Takaaki Wajima

Tantalum capacitor is a small-sized and has large capacity, and is indispensable for electric equipment. The demand increases year by year, and a quite large number of used tantalum capacitors is generated. Recovery of tantalum from tantalum condenser is recently important since production of tantalum have not been stable for the price and the quality. However, recovery of tantalum from tantalum-condenser is difficult since tantalum parts strongly cover with the flame retardant resin made of halogenated compound (mold resin). This research investigated recovery of tantalum parts from tantalum condenser using steam gasification with mixed molten carbonate. Mixed molten carbonate (Na2CO3:K2CO3:Li2CO3 = 1:1:1) (3 g) put into the reactor, and heated with electric furnace while flowing nitrogen (160 mL/min) and steam (1 mL/min) warmed by heater. After heating to setting temperature (450 - 650 oC), tantalum condenser (3 g) was put into the reactor, heated for 5-10 min, and then cooled to room temperature to recover the reacted capacitor by filtration after treating with distilled water. At relatively low temperature (550 oC) heating for 10 min, mold resin can be decomposed by using steam gasification with mixed molten carbonate, in comparison with using pyrolysis and steam gasification without carbonate, and decomposition reaction occurred over 500 oC by using steam gasification with mixed carbonate. Recovery of tantalum parts from capacitor is successful using steam gasification with mixed molten carbonate at 530 oC for 5 min, due to the effective decomposition and removal of mold resin from capacitor. Furthermore, most halogen gas generated from decomposition of mold resin can be trapped in molten carbonate not to exhaust halogen gas. These results suggested that recovery process of tantalum parts from used condenser using steam gasification with mixed molten carbonate is expected as a feasible way to recycle the rare metal in electric equipment.

Jan 1, 2014

By Ersin Yazici, Ahmet Bas, Haci Deveci

Pregnant leach solutions from waste of printed circuit boards (WPCB) leaching contain many impurity metals (Fe in particular) at significant levels. These impurities should be reduced to acceptable levels to avoid problems in downstream recovery processes e.g., low current efficiencies in electro-winning of copper from sulfate solutions in the presence of ferric. In this study, removal of iron in the form of goethite from synthetic (30 g/L Cu2+ and 1 M SO42-) and real leach solutions of WPCB was studied in some detail. The influences of initial concentration of iron (1-4.5 g/L Fe3+), pH (2.5-4.0), temperature (80-90°C) and seeding (23.5 g/L) were investigated over a period of 4 h. A significant increase in the iron precipitation was observed (i.e., from 68% to 96% over 4 h) with rising the pH from 2.5 to 4.0. The addition of seeds had also increased the removal rate over 4 h albeit to a limited extent i.e., from 96% to 99%. For the real leach solutions of sulfate (H2SO4-H2O2) and sulfate/chloride leaching (H2SO4-CuSO4-NaCl), precipitation of iron was found to be 63-73% (pH 2.5) and 93-98% (pH 4.0), respectively. The precipitates were further characterised by SEM-EDS analysis which showed the presence of copper (1-25%) in the precipitates indicating significant copper co-precipitation from the solution. These copper losses can be attributed to the formation of copper compounds such as anthlerite and brochantite within the range of pH (2.5-4.0) tested. This study showed that iron can be readily removed from synthetic/real leach solutions of WPCBs to a large extent (=93%) at the expense of high copper losses particularly at pH 4.0.

Jan 1, 2014

By E. Lee

With the growing environmental concern, as well as the increasing concern for sustainability of natural resources, the need of improving the performance and efficiency of today?s crushers is be-coming increasingly important. However, the development of existing crushers requires an extended basic knowledge about the crushing process itself. The aim of the present study is therefore to find the theoretically optimal way of crushing compressively under given circumstances. In the present paper, optimizations have been performed with the purposes of maximizing product yield and minimizing energy consumption. Performed on an ideal crushing stage free from physical limitations, the optimization results have been obtained in terms of number of compressions and their corresponding compression ratios. Complementing earlier results on interparticle breakage (Hulthén et al., 2006), presented here are thus the results from corresponding optimizations with single particle breakage and interparticle breakage. It is concluded that modern crushers are not working optimally in any of the studied aspects for gneiss. In fact, optimizations indicate that a lowering of the compression ratio, as well as a shortening of the crushing sequence, are theoretically favourable. The outcome of this study is therefore highly promising as to giving new ideas and suggestions of improvements in existing crushers, and can even result in redesign of compression crushers.

Jan 1, 2014

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

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

Jan 1, 2003

By J. Yvon, Inna V. Filippova

"The aim of this work is to seek the inhibitors of the meteoric and bacterial dissolution of sulphides and gangue minerals to stop the undesirable chemical reactions during conservation of the flotation wastes. The approach of passivation of surfaces by chemical treatment of the solid phase is applied for this objective.The samples taken from different depths of an old French waste dump revealed the capacity of the flotation tailings to produce acid waters (pH 1.8-2.4) and to release heavy metals. Mineralogical studies show not only the product of sulphide oxidation, i.e. sulphates, but also the complex transformations of aluminosilicates in acidic liquid phase. The detection by XRD of aluminium hydroxides (gibbsite, boehmite) allows supposing the recrystallisation phenomena during tailings conservation.Comparative tests of the passivation of the surface of sulphide minerals and waste of flotation with using of conventional reagents (CaO, NaOH, phosphates) and original reagents for this purpose (alkyl dithiocarbamates) allow to identify the optimal treatment conditions and the efficient chemicals.Leach tests were carried out in percolation columns during 68 weeks. The normalised leaching tests according to French legislation were run to confirm the selected treatment conditions. The results obtained show that a single treatment with carbamate inhibits the oxidation of the pyrite and the other sulphides, and totally prevents the formation of acid waters (the stabilised pH was 5.3-5.8). Treatment of in situ drainage water allows to obtaining a total precipitation of heavy metals: the residual concentrations of Fe, Cu and Zn are lower than 0,1 mg/l.The passivation of sulphides is the result of the formation with carbamate (studied by IR spectroscopy and XPS) of organometallic compounds, which are stable in acid medium. The presence of thiuramdisulphide (product of alkylcarbamate oxidation) at the mineral surface stabilises the mixed adsorption layer and leads to a considerable reduction in the hydratation rate of surface by avoiding the corrosion of the pyrite. No aluminium was detected in leach solution with this treatment."

Jan 1, 2003

By A. N. Zagorodnyaya, Ye. G. Bochevskaya, E. A. Sargelova, Z. S. Abisheva, A. S. Sharipova

"In Kazakhstan, there is a unique sulphide copper deposit, in the ores containing the natural isotope of osmium-187 (more than 90 %). In the pyrometallurgical processing of concentrates for the target metal, osmium is mainly sublimated, with wet cleaning of metallurgical gases (dust and gas mixture) 40 % of it together with rhenium passes into washing solutions (wash acid). On the basis of this acid, the production of ammonium perrhenate was organized at the enterprise of the RSE ""Zhezkazganredmet"" and for the first time in the world practice - the isotope of osmium-187. However, the degree of its recovery from solutions does not exceed 8 % of the amount supplied with the charge or 25 % of the amount that was received for extraction. But the bulk of it (~ 75 %) remains in the raffinate, discharged to sewage treatment plants (wastewater). The studies presented in this work are aimed at solving the problem of osmium isotope-187 extracting from wastewater, which are a potential source of increasing metal production in Kazakhstan. The aim of this work is the development and scientific justification of osmium deposition regimes from wastewater using such reagents as thiosulfate and sodium sulphide. The influence of various physicochemical factors on the precipitation of the osmium was studied and optimal conditions for its maximum transition to sediment were chosen. An original method for obtaining osmium concentrate in the presence of sodium thiosulfate with the addition of potassium iodide from a new type of wastewater - man-made ammonia solutions has been developed. These solutions were combined mother liquors of solid-phase stripping operations and dissolution of pulp of crude ammonium perrhenate. On the basis of the obtained results, a settling technology for extraction of the osmium from man-made ammonia rhenium-containing solutions was introduced at RSE ""Zhezkazganredmet"". It should be noted that the degree of extraction of osmium, depending on its concentration in solutions entering on the settlement, and taking into account the addition of sulfuric acid, will vary from 60 to 90 %. The recovery of osmium during the test period was 58 %."

Jan 1, 2018

By Minna Päällysaho

For the first time, the idea of sustainable development was recognised at a high political level at the UN Conference on Environment and Development held in Rio de Janeiro in 1992 (UNEP, 1992). Then the governments of the world committed themselves to promote sustainable development in their national activities and international co-operation. In 2001, the European Council approved the EU Strategy for Sustainable Development (European commission, 2011). This complements and supports the EU?s so-called Lisbon Strategy (European council, 2000) on competitiveness. The revised Strategy for Sustainable Development was approved in June 2006. Recently sustainability has had an important role in policy and decision-making while the public awareness towards limits of the environment has been rising. However, the indicators of industrial sustainability satisfy primarily the needs of corporate management and global investors. The information is often broad and non-specific and might occasionally even give a false impression. Moreover, contradictions between environmental, economical and social aspects also point out the unreliability of existing sustainability indexes. Therefore, the current state of affairs serves the interests of neither the industry nor the policy makers. Current corporate sustainability indexes and indicator systems need to be assessed with scientific methods encompassing the identification of their strengths and weaknesses. This requires quantitative and qualitative assessment and synthesis of existing indexes and indicator systems, providing new data on the functionality of existing corporate sustainability indicators. Therefore, the assessment lays the foundation for the development of new, more balanced sustainability index. Our first aim in this multidisciplinary article is to analyse existing global sustainability indexes for process industry. Second, we will introduce a first version of a new sustainability index for process industry, which includes the environmental, social and economic impacts of the plant, as well as legislation aspects.

Sep 1, 2012

By Herman Mendoza, Luisa Ciriaco

An investigation of the seeding mechanism using heterocoagulation and the Derjaguin - Landau - Verwey - Overbeek (DLVO) theory of two pure minerals is the objective of this study. The seed was silica with modal diameters of 4.529 µm (fine particles) and 5.216 µm (coarse particles) and the test powder was hematite with a modal diameter of 0.883 µm. Parameters included variations in the concentration and particle size of silica. Both particles were first subjected to size determination and settling tests via Stoke’s Law. The silica-hematite system was then suspended in 0.001 M KNO3 electrolyte solutions where pH was adjusted. Afterward, the suspension was agitated and was allowed to settle at different time intervals while obtaining turbidity readings. Results through settling time and turbidity vs. pH graphs indicate that maximum heterocoagulation occurs from pH 2 to 5 while minimum heterocoagulation occurs from pH 6 to 7. At these pH levels the zeta potentials of silica and hematite are negative and positive, respectively. On the contrary, repulsive forces dominate the system from pH 8 to 11 due to the particles’ negative zeta potentials. Furthermore, the attachment of hematite to silica increases when the parameters become larger thereby increasing the effectivity of heterocoagulation at acidic to neutral pH levels.

Jan 1, 2014

By F. O. Milovich, V. A. Ignatkina, L. A. Samatova, E. D. Shepeta

"The aim of the research was to increase technological parameters of the flotation of finely disseminated scheelitecarbonate ore using selective reagent regime.In the studies the monomineral fractions of scheelite and calcite; samples of the scheelite-carbonate ore of the Primorsky deposit with the range of the carbonate module 3-65 were used. A carbonate module of ore is the ratio an initial assay of calcite to an initial assay of scheelite. Sodium oleate, iso-decyl alcohol, water glass, calcium chloride, soda or sodium hydroxide as flotation reagents were used. The flotation method in the Hallimond tube and in a mechanical cell, an adsorption method for study the kinetics of adsorption of oleate and isodecyl alcohol and its combinations on scheelite and calcite, IR spectroscopy including ATR to study the composition of surfacecompounds were applied. Selective reagent regime may include two ways - a combination of collectors or a modification of depressants of calcite and other gangue minerals. On one hand the combination of sodium oleate and higher fatty iso-alcohols of fractions C12-C16 in the rough scheelite flotation to reduce the flotation activity of calcite has been studied. On the other hand depression of calcite flotation by calcium chloride with water glass into rough flotation was used; modified the steaming cycle by Petrov's method applying change the concentration of water glass and other. Fatty iso-alcohols can adsorb on the surface of the calcite that reducing the adsorption of sodium oleate and floatability of calcite has been fallen. Their co-adsorbing with oleat on the scheelite surface were support the hydrophobization and flocculation of slime particles of scheelite. Flocculation of the particles of scheelite leads to increased up 3 times of the recovery of scheelite from the slime class, and calcite change up only 1.4-1.1 times it’s recovery.The growth of the carbonate module more than 11 is decreased the assay of WO3 in the scheelite concentrate of selection cycle."

Jan 1, 2018

By Xiao Jian Li, Dai Xiong Chen, Jian Wen Yang

In one kind of lead and zinc bearing polymetallic ore containing secondary copper, the characteristic of low sulfur, high zinc, and particularly the existing of secondary copper minerals can lead to lead concentrate with high content of zinc because the dissociation of Cu2+ in the grinding process may have an activation influence on sphalerite. Considering its process mineralogy analysis, a new process of seperation of lead and zinc has been put forward. The experiments focused on the analysis of the advantages and disadvantages of the inhibition effect of traditional adjustment reagent + zinc sulfate on activated sphalerite compared with new organic inhibitor, polysaccharide xanthate. According to the numerical calculation and test results, a reagent system of polysaccharide xanthates is developed, which has a good inhibition effect on Cu2+ activated zinc minerals, achieving high-efficiency separation of lead and zinc. A new reagent system and flotation process was developed under optimal conditions. Under the condition of the run-of-mine ore containing 2.37% Pb and 12.48% Zn, lead of 67.69% grade and lead concentrate with the recovery rate of 86.06%, zinc of 60.32% grade and zinc concentrate with the recovery rate of 96.15% were achieved.

Jan 1, 2014

By H. Koca, D. O. Aksoy, S. Koca

"In this work, modelling of galena flotation from a disseminated Pb-Zn ore containing 0,83 % Pb was investigated. In the flotation experiments, collector type and amount, frother type and amount, particle size, pH and flotation time were kept constant while solid ratio and depressant dosage were varied. The varied parameters are described with a mathematical model by using statistical design method. Central Composite Design method which is one of the principle response surface methodologies was used in statistical design and analysis of experimental results and process modelling. Two quadratic mathematical models were developed for Pb grade and Pb recovery. Analysis of variance showed that models obtained for Pb grade and Pb recovery were found to be statistically significant in 95 % confidence level. Predicted vs actual values of Pb grade and Pb recovery were also given in graphically. It was found that predicted values represent approximately 96 % and 94 % of actual Pb grade and Pb recovery, respectively. The high values of R-square (R2) indicate that the models developed for two response variables are powerful. INTRODUCTION Lead and zinc metals are widely used in electrical, mechanical, military, metallurgical, chemical, light and medical industries. Sulfide ores are the main resources for lead and zinc minerals (Luo et al., 2016). Froth flotation is the main beneficiation method to achieve lead and zinc sulfide minerals separation. There are two basic approaches to obtain lead and zinc separation by flotation. First, flotation of lead sulphide is carried out and zinc sulphide and gangue minerals are depressed by various depressants and second, the bulk flotation of lead and zinc sulphide is carried out to obtain a concentrate of lead and zinc, followed by the lead and zinc separation. (Yuan et al., 2012). Apart from concentration of lead and zinc by flotation, there are a few literature that reports concentrations of lead and zinc by gravity and hydrometallurgical methods with remarkable success (Goktepe, 2005; Yanbo et al., 2016)."

Jan 1, 2018

A new short combined flow sheet including high intensity magnetic separation and flotation for a rare earth ore in Maoniuping deposit, China has been investigated. Massive conclusive results demonstrate, that it is critical to separate the ore by high intensity magnetic separation prior to flotation for tons of slimes and nonmagnetic gangue existing. The vital technological parameters affecting flotation have been studied in detail. Modified hydroxamic acid is an efficient collector for bastnasite flotation because of its high selectivity. Flotation results also indicate high temperature that play an unfavourable role on the recovery as well as the grade of bastnasite concentrate, when the rare earth ore is floated with modified hydroxamic acid and sodium silicate depressant. Bastnasite concentrates, averaging over 65 percent REO at an overall recovery of 82-84% is achieved by the new beneficiation technology. Keywords: bastnasite, REO, magnetic separation, flotation, chelating collector, desliming

Sep 1, 2012

The concept of the Unified Comminution Model (UCM) was presented at the 23rdIMPC. The model utilises computational techniques to calculate the mechanical environment in any comminution device, and then incorporates the outcomes from rock breakage tests to predict the product from a device. The model is fully mechanistic, and incorporates the capability to simulate novel equipment. This paper presents the progress on the first application of this concept to applied comminution equipment. This novel comminution model aims to integrate all comminution models within a single struc-ture. This will provide a step change in the predictive power of comminution models, and include a wide range of particle properties that will enable it to be linked to the upstream and downstream process of mining and recovery. Major advances over current models will be the capability to predict liberation, preferential grinding, performance of new and novel devices, and to have power as an integral driver of the comminution simulation process. The methodology and model structure have been developed. An equation within a population balance framework has been derived as the basis for the UCM. A set of SAG mill pilot has been used as the first test case. The breakage characteristics of the ore have been extensively tested utilising a new range of breakage tests required by the rigorous UCM structure. The mill was simulated with the EDEM - DEM software. A partial test simulation of the pilot SAG mill has been conducted. This serves to demonstrate the feasibility of this modelling technique, but still lacks important ore characterisation components that are under development. The study has raised a number of significant challenges to the accepted understanding of the comminution process. Through addressing these challenges considerable insight has been gained into the energy environment in mills and the requirements of breakage testing. The ore characterisation methods and energy transmission derived from DEM simulations remain as major research items.

Jan 1, 2014

By Alexander E. Sobolev

The kinetics of oxidative dissolution of lead sulfide in solutions of nitric acid and sodium hypochlorite was studied using the rotating disk method and the factor experiment design. The dependences of the PbS dissolution rate on concentration of oxidant (HNO3 or NaOCl), temperature, disk rotation frequency, and duration of interaction were determined. The adequate kinetic models allowing calculating the specific dissolution rate at any combination of values of the influencing factors were obtained. As a result of the complex analysis of kinetic parameters, the modes of the each process proceeding were established, their macromechanisms were determined, and the limiting stages of the oxidative dissolution processes were revealed. The dissolution kinetics of lead sulfide in solutions of nitric acid was found to have several regimes. At HNO3 concentrations below 0.5 mol/L, the process proceeds in a mixed mode close to a diffusion-controlled. It is caused by low oxidative activity of HNO3 and considerable diffusional diffuculties at this acid concentration range. At the nitric acid concentrations more than 0.5 mol/L and less than 6.0 mol/L, the process was found to be kinetically controlled. The limiting stage of the interaction is the surface chemical reaction. The observed relatively high order of the dissolution rate with respect to the concentration of HNO3 was explained by the autocatalytic action of the acid reduction products. At nitric acid concentrations exceeding 6 mol/L, the process proceeds in a mixed mode close to a diffusion-controlled, and the dissolution rate sharply decreased that was explained by a decrease in the solubility of reaction products. When lead sulfide is dissolved in sodium hypochlorite solutions, at first time the amount of PbS transferred into solution remains close to zero. Gradually, as time goes, this amount begins to increase sharply. The dissolution rate rises and reaches the maximum value, further remaining constant. At the steady-state regime, the dissolution rate is independent of the duration of interaction and disk rotation frequency. The process was found to be kinetically controlled. The limiting stage is likely to be chemical reaction on the surface of solid lead sulfide. The obtained kinetic characteristics enlarge the database on hydrochemical oxidation kinetics of sulfides and can be used for the elaboration of the recommendations for the effective comprehensive exploitation of lead-bearing ores and concentrates. Keywords: lead sulfide, nitric acid, sodium hypochlorite, hydrochemical oxidation, dissolution kinetics

Sep 1, 2012

By M. Karamoozian

Modelling and optimisation of the power draw of large SAG mills are important due to the large power draw which modern mills require (5~10 MW). The cost of grinding is the single biggest cost within the entire process of mineral processing. Traditionally, modelling of the mill power draw has been done using empirical models. Although these models are reliable, they cannot model mills and operating conditions, which are not within the model database boundaries. Also, due to their static nature, the impact of the changing conditions on the power draw, within the mill, cannot be deter-mined using such models. Despite advances in computing power, on-line modelling of large plant scale mills could be a time consuming task. On the other hand, using on-line parameters for model-ling, result in more reliable control of SAG mill without performing any more costly tests. In this paper, SAG mill power draw is modelled using neural network approach. Six inputs, namely: solid percent, two bearing pressures, noise, recycle and feed rate were used to model the power draw. The produced model shows an acceptable correlation coefficient, R2 =0.9623.

Jan 1, 2014

By V. G. Minenko, V. A. Chanturiya, A. L. Samusev

Eudialyte is one of perspective resources of zirconium and other rare earth elements (REEs). Large reserves of eudialyte concentrated in the Murmansk region of the Russian Federation. Usually, technologies of REE treatment include the decomposition of eudialyte concentrate in different acidic, extraction and utilization of all components. The main problems in the leaching of eudialyte include are: the formation of an unfiltered silicon-containing gel; low recovery of REE; difficulty extraction of metals from the productive solution; high aggressiveness of the reagents. One of the promising trends of intensification of the processing of hard-to-degrease rare metal raw materials is the use of energy methods for affecting mineral suspensions. These methods make it possible to increase the efficiency of break up fine-dispersed mineral complexes and extracting micro- and nanoparticles of a valuable component in subsequent deep processing. The purpose of this work is to investigate the effect of energy impacts on the nitric acid leaching of eudialyte concentrate. Experimental studies were carried out in a developed laboratory facility that makes it possible to evaluate the effect of electrochemical, ultrasonic and combined effects on the leaching of zirconium and REE from eudialyte concentrate. The studies carried out on the samples of eudialyte concentrate with the size class of -0.315 + 0.063 mm showed that the use of electrochemical and acoustic effects increases the extraction of ZrO2 in the production solution in 1.6 - 2.5 times, REE in 1.3 - 2.2 times, respectively. An analysis of the microstructure and phase composition of the surface of the eudialyte concentrate showed that the intensification of the leaching process is due to surface cleaning from the silicon-containing gel, as well as the opening of capillary channels and microcracks, which accelerates mass-transfer processes. The results obtained open wide opportunities for creation of modern and effective technology of processing of eudialyte concentrate, producing high-quality zirconium products and REE.

Jan 1, 2018