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By Francis Pitard

"The optimization of metallurgical processes requires an in-depth understanding of the heterogeneity carried by any constituent of interest. It emphasizes that knowledge of the Theory of Sampling (TOS) is the necessary step to ensure that valuable and valid research programs, pilot plants, feasibility studies, plant design and plant operations have been set on solid foundations. Too many publications today are solely based on the properties of the sample, with no mention of how this sample relates to anything in the environment where it was collected. Unfortunately sampling is an error-generating process that leaves no apparent tracks of its shortcomings. Indeed, it is easier to track down analytical errors than sampling errors. Consequently, bad sampling practices plague the scientific community and the industry and are responsible for severe money losses, unsatisfactory science and processing, and sometimes litigation. A point-by-point strategy is presented addressing sampling problems in early stages of a project. Sampling system requirements for metallurgical accounting and process control are listed. The use of Chronostatistics is suggested to determine if sampling systems are performing satisfactorily and to identify the various types of process variability that may not be easily detected by a conventional inspection of available chronological data. This strategy will help engineering firms, manufacturers, managers and supervisors to provide, install, use and maintain key sampling systems located at very important points in a process. Equipped with the appropriate sampling and statistical tools it becomes easier to minimize reconciliation problems with the mine, with suppliers and with clients. Contrary to the beliefs of many people, good sampling systems are not expensive because in the long run they help to reduce hidden cost and better regulate plant productivity; they most certainly minimize the number of unnecessary meetings looking for solutions where there are none. The suggested strategy will help specialists to extract maximum information from the available data, as large investments and crucial decisions depend on it."

Jan 1, 2014

By Hermann Wotruba, Lars Weitkämper

"Dry coal dressing was popular during the 1950.s and 60.s in many parts of the world. The devices mainly used were air jigs and air tables.The increase in ash and moisture content of run-of-mine coals due to the wide advanced mechanisation of mining mechanisation during and after this period led to that pneumatic devices being unable to treat run-of-mine coals with the desired efficiency. Since the 1960.s almost all new coal preparation plants have been based on wet processes that are highly efficient in terms of coal recovery and their ability to handle damp and sticky run-of-mine coals. (Frankland, 1995)However, water is becoming increasingly costly and the disposal of fine products, containing most of the water, is an environmental concern. There would be significant cost savings and a lower total energy consumption if coal could be cleaned dry. Efficient dry coal treatment would be an interesting solution in desert, arid or cold areas.In Germany one dry coal dressing plant is in operation. The process and the advantages and disadvantages are presented below.Further on new developments in the field of dry density separation of coal are reviewed and analysed. Test results of new dry coal separation methods e.g. new developed air jig and magnetic separator are reported."

Jan 1, 2003

By A. Ekrem Yüce, Gülay Bulut, Feridun Boylu, Vecihi Gürkan, Istanbul Technical University, H. MustafaTarkan

"Nickel sulphide ores subjected to this investigation were taken from Orhaneli district where widespread chromite mineralisation can be occurred. Significant amounts of magnetite and chromite have been existed in the ore together with sulphide and oxide type nickel minerals. Ore sample is constituted about 70% magnetite, 15% sulphide minerals, 5% chromite and iron oxides as well as 10% gangue minerals.According to the chemical analysis results, the representative ore sample contains 1.32% Ni, 10.8% SiO2, 78.4% Fe2O3, 1.3 g/t Ag and 1.0 g/t Au. Mineralogical examinations showed that pentlandite (Fe, Ni)9S8, violarite (Ni, Fe)3S4, millerite NiS and asbolane (Co, Ni)MnO2.(OH)2.1-2H2O were the main nickel minerals and magnetite, chromite, chromium spinals, pyrite, pyrhotite, chalcopyrite, cubanite, goethite, hematite, limonite, rutile, chlorite, talc and serpentine group minerals as associated minerals.The aim of this investigation was to produce valuable nickel concentrates by using gravity separation, magnetic separation and flotation methods. As a results of laboratory scale studies, alternative flow sheets for the production of nickel sulphide concentrate were developed. The related experimental results are given in Table 1."

Jan 1, 2003

By Hideki Yamamoto, Norihiro Murayama, Junji Shibata

"Hydrothermal syntheses of zeolite from coal fly ash were carried out by using various alkali sources. NaOH, Na2CO3, KOH, K2CO3 and their mixture were applied for an alkali source of zeolite synthesis. The various physical properties of the reaction product, such as the kind of zeolite crystal, cation exchange property, surface texture and so on, was investigated through the zeolitization reaction from fly ash. The mechanism of zeolitization reaction was considered from these results.Zeolite P(NaP), hydroxysodalite(HS) and chabazite(K-CHA) are synthesized as zeolite species, when fly ash hydrothermally reacts in various alkali solutions at 393K. The crystal structure of the products obtained in NaOH solutions for 3h changes from NaP to HS with increasing NaOH concentration. K-CHA formation in KOH solutions needs 10h of reaction time, which is longer than that of NaP or HS.Dissolution, condensation and crystallization steps exist in the zeolitization reaction from fly ash, and the particle surface of products remarkably changes in each step. The fly ash is spherical particles and the surface is smooth(Fig.1(a)). The dissolution of fly ash occurs in the heating process until 393K, and the particle surface changes like unevenness(Fig.1(b)). In case of NaP, the condensation of aluminosilicate ions takes place at 373-393K, and the amorphous aluminosilicate is deposit on the unreacted fly ash(Fig.1(c)). The crystallization of NaP already begins to occur at 393K and the surface is covered with fine zeolite crystals for 24h(Fig.1(d))."

Jan 1, 2003

By Aziza A. Yousef, Suzan S. Ibrahim, Mahmoud A. Arafa, Mohamed A. Abdel Khalek

Due to the shortage of fresh water in the Middle East, seawater has been used as an alternative in flotation beneficiation. The flotation process requires about 7 m3 of water/mt ore. This article aims to study the effect of seawater cations and anions on the flotation. Natural pure francolite, calcite, dolomite and quartz were characterized by chemical, thermal and x-ray diffraction analyses, surface area, solubility and zeta potential. Synthetic seawater was prepared with the major chemical composition similar to natural seawater as follow; 2.45% NaCl, 0.52% MgCl2, 0.41% Na2SO4, 0.116% CaCl2 and 0.07% KCl. Also, natural seawater was used in application. The point zero of charge was estimated at pH 6.5, 7.8, 9.2 and 2.2 for francolite, calcite, dolomite and quartz, respectively. Calcium ions were released from the three minerals with Mg2+ and P2O5 3– released from dolomite and phosphate, respectively. The adsorption of collector, zeta-potential and floatability of pure minerals were studied. The effect of individual cations and anions predominant in seawater are studied on individual mineral or group. The troublesome Ca2+ and Mg2+ ions should be controlled by soda ash addition. Sodium silicate improved the selectivity of mineral mixtures and natural ore. At optimum conditions the calcareous phosphate ore yielded a concentrate of 34% P2O5, at 83% recovery with 0.61% MgO, from an ore assaying 25.3% P2O5 and 9.4% MgO. To minimize the Clcontent, fresh water of about 0.5 m3 /t was used and the Cl- decreased to about 0.09 %

Jan 1, 2003

By Lev Malytin, Alexander Dyachenko, Roman Kraydenko

"A new method of processing beryllium raw materials based on interaction of beryllium mineral with ammonium fluoride was developed. Possibility of extracting ammonium tetrafluoroberyllate from bertrandite and phenakite minerals is proved. The developed technology allows replacing the outdated sulfate technology developed by Materion Corporation. INTRODUCTION Beryllium is a strategic metal, which is produced only in three countries: the USA, China and Kazakhstan. The world production of beryllium amounts to only 300 tons per year. More than 75% of the world beryllium production is manufactured from oxide beryllium ores in the USA by Materion Corporation. In Russia there is a large-scale beryllium ore deposit «Ermakovskoye» containig over 1 million ton of ore. Concentration of beryllium in ore amounts to 1,2%. Since the mineral base of ore is calcium fluoride, the sulfate technology of Materion Corporation cannot be used. After alloying and sulphuric acid leaching the fluorine-ion found in fluorite and beryllium together evolve into the aqueous phase. At the stage of Be(OH) precipitation fluoride-ion prevents complete isolation of beryllium into the phase of hydroxide, which increases the loss of beryllium. A new ammonium-fluoride method for processing high-fluoride beryllium ores has been developed at Tomsk Polytechnic University. The ammonium-fluoride method involves fusion of ammonium fluoride (NH4HF2) with a beryllium concentrate. The concentrate containing 10% of beryllium oxide and 25% of calcium fluoride is produced by flotation from the ore of Ermakovskoe deposit. The main component of the ore concentrate is fluorite CaF2, which does not react with NH4HF2. Beryllium in this concentrate is represented by two minerals: phenakite Be2(SiO4)2 and bertrandite Be4[Si2O7](OH)2. Ammonium fluoride, unlike sulfuric acid, does not react with calcium fluoride and is not consumed for decomposing the mineral base of the concentrate. Ammonium fluoride is an accessible and environmentally safe reagent, worth up to $ 1,200 per ton. The total amount of ammonium fluoride is recycled and is used for decomposing a new batch of beryllium concentrate."

Jan 1, 2018

By Lev Malytin, Alexander Dyachenko, Roman Kraydenko

"A new method of processing beryllium raw materials based on interaction of beryllium mineral with ammonium fluoride was developed. Possibility of extracting ammonium tetrafluoroberyllate from bertrandite and phenakite minerals is proved. The developed technology allows replacing the outdated sulfate technology developed by Materion Corporation. INTRODUCTION Beryllium is a strategic metal, which is produced only in three countries: the USA, China and Kazakhstan. The world production of beryllium amounts to only 300 tons per year. More than 75% of the world beryllium production is manufactured from oxide beryllium ores in the USA by Materion Corporation. In Russia there is a large-scale beryllium ore deposit «Ermakovskoye» containig over 1 million ton of ore. Concentration of beryllium in ore amounts to 1,2%. Since the mineral base of ore is calcium fluoride, the sulfate technology of Materion Corporation cannot be used. After alloying and sulphuric acid leaching the fluorine-ion found in fluorite and beryllium together evolve into the aqueous phase. At the stage of Be(OH) precipitation fluoride-ion prevents complete isolation of beryllium into the phase of hydroxide, which increases the loss of beryllium. A new ammonium-fluoride method for processing high-fluoride beryllium ores has been developed at Tomsk Polytechnic University. The ammonium-fluoride method involves fusion of ammonium fluoride (NH4HF2) with a beryllium concentrate. The concentrate containing 10% of beryllium oxide and 25% of calcium fluoride is produced by flotation from the ore of Ermakovskoe deposit. The main component of the ore concentrate is fluorite CaF2, which does not react with NH4HF2. Beryllium in this concentrate is represented by two minerals: phenakite Be2(SiO4)2 and bertrandite Be4[Si2O7](OH)2. Ammonium fluoride, unlike sulfuric acid, does not react with calcium fluoride and is not consumed for decomposing the mineral base of the concentrate. Ammonium fluoride is an accessible and environmentally safe reagent, worth up to $ 1,200 per ton. The total amount of ammonium fluoride is recycled and is used for decomposing a new batch of beryllium concentrate."

Jan 1, 2018

By Özcan Y. Gülsoy

Coal beneficiation with optical sorting has not yet been studied in detail. Optical separation of coal from gangue particles as a dry method can be used as an alternative to the other enrichment methods. Developments in optical and pneumatic technology put the optical sorting one step forward by means of applicability of the mechanical sorting to the mineral industry. Because of the inefficient separation performance, dry separation of coal is very limited in industrial applications. Therefore, optical sorting depending on color differences between two minerals can be introduced to coal beneficiation systems. In this study, coal samples obtained from Konya-Ilgin region (Central Anatolia-Turkey) were separated by optical sorter and the results were evaluated. The conventional floatability tests for Ilgin coal are conducted by collecting most of the feed material at 1.3-1.4 g/cm3 density range. Separation of Ilgin coals with heavy medium methods will not be possible because of poor density difference between coal and its impurities. There are important color differences among the floated particles at 1.3-1.4 g/cm3 density range. Therefore, Ilgin coal is subjected to optical sorting in a pilot scale optical sorter. Different size fractions were fed to the optical sorter and then rejected and accepted particles by equipment were analyzed. Ash content of the accepted particles was reduced to 25-35 % and ash in tail increases up to 55-60 % after sorting. Although most of the material floated at low densities, optical sorter separated the feed into two different quality products. This study has the potential to clarify applicability of optical sorting even to non-floatable coals and to provide an important contribution to both industrial applications and literature.

Sep 1, 2012

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

By Graeme J. Jameson

In conventional flotation machines, the recovery is strongly related to particle size. As particle size increases, the recovery also increases, reaching a maximum in the range 20 to 120µm. Beyond this range however, the recovery declines quite quickly. The reason for the decline in recovery observed with coarse particles can be traced to the effect of turbulence. Bubbles trapped in turbulent eddies rotate rapidly, and when the centrifugal force on a particle exceeds the retaining forces due to surface tension, the particle detaches. Since the centrifugal force varies as the cube of the diameter of the particle, and the attachment force varies simply as the diameter, being proportional to the length of the contact line, it is clear that detachment forces will predominate as the particle size increases. The corollary is that the recovery of coarse particles can be improved if the level of the turbulence in the cell can be reduced to a minimum. In this paper, a new type of flotation machine will be described, in which the particles to be floated are suspended in a fluidized bed. An up flow of fluidizing water is provided, by recycling liquid from the top of the cell. The recycle stream is aerated in a high-energy device that disperses the air into fine bubbles that capture the fines and ultrafines. Results are presented for several minerals and coarse coal. Keyword: fluidized bed flotation

Sep 1, 2012

By James Y. Oldshue

"Very seldom is it possible when contacting a gas with a slurry to measure the dissolved gas concentration in the slurry, and even where possible, equilibrium data with a suitable Henry.s law constant are seldom available.In general, by assuming a reasonable value for the dissolved gas concentration in the slurry and a corresponding equilibrium gas partial pressure P*, KGa values can be calculated for the pilot plant and then scaled up. Then, with the same P* value at various reaction conditions, a mixer can be designed which is quite satisfactory, having a reasonable design factor for full-scale performance."

Jan 1, 2003

By Y. E. Brylyakov, M. A. Kostrova

"The apatite staffelite ores (ASO) of Kovdor deposit are dominated by fine-grained aggregates containing both phosphate minerals and silicates — vermiculite, smectites, zeolites. These minerals exhibit ion-exchange properties. In this connection, the magnitude of cation exchange, along with the content of P2O5 and CO2, is an important property of apatite staffelite ore, which largely determines the performance of concentration processes. In the examined ASO samples, the magnitude of cation exchange measured in terms of Ca2+ is 2546-4790 g/ton. The conducted laboratory studies of apatite staffelite ores with various mineral composition showed that adding calcined soda improves the recovery of P2O5 into the flotation concentrate. Full-scale tests were conducted at the apatite staffelite ore processing plant at Kovdor Mining and Concentration Operation and demonstrated the high performance of the proposed agent treatment. The test results showed that in the flotation of apatite staffelite ores, the optimum calcined soda feed rates range from 3,500 to 5,000 g/ton of the flotation feed. With close flotation feed and concentrate grade parameters, the P2O5 recovery gain is 17%. The effect of adding soda is associated with the desorption of the hardness cations from the minerals, precipitation in the pulp and, accordingly, improvement in the ionic composition of the liquid phase of the flotation feed due to a reduced content of calcium ions. Based on the test results, the proposed agent treatment with an elevated feed rate of calcined soda was implemented at Kovdor Mining and Concentration Operation in the flotation of apatite staffelite ore. The apatite staffelite ores (ASO) of Kovdor deposit are dominated by fine-grained aggregates containing both phosphate minerals and silicates — vermiculite, smectites, zeolites. These minerals exhibit ion-exchange properties. These minerals have certain properties requiring a more detailed examination for a better understanding of the flotation properties of apatite staffelite ores."

Jan 1, 2018

By Milind Chikhale, Yogesh Reja, Keshav Tyagi

"Using computer models for process design is a well-established practice in the mineral industry. In recent years, there has been emphasis on modeling of processing plant as a whole. This paper covers development of a model for iron ore processing plant. Basic purpose of this model is to use simulation for efficient plant design and help in minimizing risk at the very initial stage of project. Feed to the plant is Hematite iron ore from a deposit located in Eastern India. Major processes in plant include multi-stage crushing, screening, grinding, classification, gravity and magnetic separation. Models for different process equipment were developed using METSIM and Bruno simulation software. Customized black box models and known mathematical models were used for predicting behaviour of processes. Data needed was identified based on the model type. The required data was arranged as per project requirement and processed for development and validation of model. Equipment models were developed and validated on the basis of process design basis, theoretical and empirical data from technical references, and bench scale and pilot scale testwork results. Validated process circuits were assembled to simulate and represent the entire plant process. The result shows expected variation in plant output as a result of variation in the feed. Study concludes by discussing potential applications of the model in plant design."

Jan 1, 2014

By Carlos Pereira, Fábio de São José, Francielle Nogueira

Votorantim Metals Corporation is one of the leader companies in the extraction of zinc in Brazil. One of its mines, located in the city of Vazante - MG, was composed by zinc silicate ores, but recent studies have indicated a change in mineralization type with arise of zinc sulphide’s ore bodies with disseminations of galena (PbS) and silver. The liberation size between sphalerite and galena in this ore occurs in very fine granulometry (approximately 18µm), fact that has negatively influenced into the flotation process. Aiming to reduce this problem, studies about the use of dispersing in the flotation process have started. Thus, this study investigated the action of different reagents dispersing on the stability of the suspensions. The tests were carried out with samples of mineral galena and sphalerite using four types of dispersing within two different dosages and two pH. The reagents tested were sodium hexametaphosphate, sodium silicate, carboxymethiylcellulose, and sodium polyacrylate. The results of the dispersion tests were analysed in relation to dispersion index. The tests with hexametaphosphate showed high dispersion for both galena and sphalerite. The sodium polyacrylate and arboxymethiylcellulose showed a high dispersion index for galena and a low index for sphalerite implying that reagent can be used in the concentration process of galena.

Jan 1, 2014

By Anuttam Patra, Romain Bordes, Andreas Fredriksson, Tommy Karlkvist, Krister Holmberg, Kota Hanumantha Rao

Almost all of the flotation reagents used today were discovered by continued application of empirical methods and/or trial and error experimentation. Moreover, with the metal-ion specific approach used so far, it is difficult to separate the minerals containing the same constituent metal ion. A critical assessment of molecular recognition processes involved in biomineralization suggested the possibility of using reagents which are surface specific. The concept that the molecules consisting of two or more functional groups having appropriate spacing between those so as to achieve structural/stereochemical compatibility during interaction with the mineral surface exhibit structure-specificity is thought to be extended to the design of specific collectors in flotation processes. In the present study, for the first time, a rational design of surface active molecules, and thereby the recognition of crystal faces (of minerals) by these molecules through structural and stereochemical matching is being utilized successfully to selectively float various minerals. For this purpose, carboxylate-based collectors (for mineral specific flotation of calcium minerals) as well as xanthate-based collectors (for mineral specific flotation of sulphide minerals) with a fixed alkyl chain length but having two functional groups with varying geometrical distances (separated by a spacer of one, two and three carbon atoms) between them have been synthesized. In this article, we have discussed the design, synthesis, purification of these novel mineral specific collectors as well as their important solution parameters in relation to flotation processes.

Jan 1, 2014

By David I. Verrelli, Boris Albijanic

"Froth flotation is an exceedingly complex physicochemical process. The convenience of distilling much of the complexity of the bubble-particle interactions into a single parameter has led to the continuing popularity of the classical ‘induction time’ to quantify the threshold for bubble-particle attachment to occur. Despite this popularity and the simplicity of the concept, there is no single universal method of evaluating the induction period. In this paper, we begin with a critical review of the available techniques for estimating the induction period. These are: back-calculation from experimental (micro) flotation tests; pushing a particle toward a stationary bubble (or vice versa) using an atomic force microscope (AFM); pushing a bubble toward a stationary bed of particles in the ‘Induction Timer’; pushing a bubble toward a stationary solid surface using the ‘integrated thin film drainage apparatus’ (ITFDA); and dropping particles onto a submerged stationary bubble using the ‘Milli-Timer’ device. Each one of these methods has advantages and disadvantages, and the best choice depends on the application. In the experimental section, we present quantitative comparison of the induction periods estimated using two different techniques, namely the Induction Timer and the Milli-Timer. The same particles were tested in each device, under the same conditions. It was found that by tuning the operation of the particle pick-up device, similar estimates of induction period could be obtained to the estimates made by direct observation with the Milli-Timer. In the former device a bubble is driven toward a particle bed at a controlled rate, whereas in the latter a particle’s motion is governed by the hydrodynamics. The potential to match these presents an intriguing prospect for better understanding the bubble-particle interaction, and the possibility to ‘calibrate’ the simpler Induction Timer against direct observations."

Jan 1, 2014

By Grigori I. Voiloshnikov

"The long-term studies on development of the technology for precious metals recovery using activated carbons executed by Irkutsk Research Institute of Precious and Rare Metals and Diamonds (IRGIREDMET) were finished by successful introduction of ""Carbon-In-Pulp"" process in Russia (1984).The review of some studies, accompanied by development, testing, introduction and subsequent improvement of considered technology, carried out by IRGIREDMET is submitted in this paper.The basic regularities of gold and silver adsorption onto activated carbons from cyanide, thiourea, chloride and other solutions are investigated using various phisical-and-chemical methods ( X-ray photoelectron spectroscopy, Voltammetry, X-ray microanalysis etc.). Using voltammetry it was found that gold cyanide is adsorbed onto activated carbon without chemical changes and partial reduction of gold is possible only during drying of carbon samples before analysis. Metallic gold and silver may be dissolved in boiling cyanide solution at argon atmosphere when they are in contact with activated carbon surface. Gold adsorption mechanism for activated carbons has great differences from that for the ion exchange resins. So the most probable mechanism for gold adsorption from cyanide solution is adsorption of neutral molecules Me n+[Au(CN)2-]n.X-ray quantitative microanalysis technique was developed to investigate gold adsorption kinetics onto spherical activated carbon. Gold profiles in granules of activated carbon for various adsorption conditions were tested (carbon particle size, mixing efficiency, adsorption time etc.). Mathematical methods were used to determine gold diffusion coefficient within activated carbon granule.The properties of various types domestic and foreign activated carbons were tested and the demands to activated carbons suitable for gold extraction were determined. As a result foreign and Russian activated carbons AG-90, AG-95 were recommended for use at Russian gold plants. Domestic adsorbents are cheaper in comparison with foreign activated carbons. The methods to restore carbon adsorption activity including acid treatment and thermal reactivation were tested and implemented."

Jan 1, 2003

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 E. V. Bratygin, S. P. Elnikova

"In the article carrying out technique of experiments for estimation of power efficiency of process of crushing in cone crushers «in a layer». The conformity of the granulometric characteristics of the crushed products obtained as a result of the tests, the theoretical equations for the size characteristics, and the choice of the optimal equation for the prediction of the granulometric characteristics of the final products obtained by crushing ""in a layer"". Optimization of granulometric composition of power of crushers working ""in a layer"" is carried out with the purpose of reduction of the electric power consumption at reception of a product of required quality. As a result of the experiments, dependencies are obtained, the relevance and applicability of the crushing process ""in the layer"" for obtaining crushed stone of improved quality is proved. INTRODUCTION A number of equations have been proposed for calculating the breakage energy. These include equations by Kirpichev and Kick, Rittinger and Bond (Bogdanov, Olevsky, 1982). Another equation for calculating the specific breakage work in breakage by impact and in stratum was proposed by Devyatkin (Boiko, 2003). In these equations, the breakage energy is proportional to the particle size raised to some power. In the equation proposed by Devyatkin, the ore piece thickness or the feed average diameter is used. The relationship between energy and breakage can be expressed as an equation (Lynch, 1981; Tikhonov, no. 3, 2008) where k is a coefficient characterizing the energy parameter depending on the strength of the feed, l is size in microns. The Rittinger formula is obtained for n = 2, the Kirpichev-Kick formula for n = 1, the Bond formula for n = 1.5. For n = 3 or higher, the equation describes fine and ultrafine grinding. R. Hookey proposed a formula (Lynch, 1981, Tikhonov, no. 3, 2008), where the size exponent n is substituted by a size function In all of the above equations, a single value of the feed and product size is used; for example, in the Bond equation, size is defined as the particle size of the 20% oversize (P80 and F80). However, a single size value can represent multiple distributions, making that the Bond method inappropriate for determining the size (Lynch, 1981). Describing an equation for estimating the grinding energy will allow to design the electric drive and ore preparation circuit for the given breakage method."

Jan 1, 2018

By S. Kelebek, A. Khan, J. Caceres, D. Beckett

"Pyrrhotite in nickel-copper sulphide ores is nickeliferrous and intimately associated with pentlandite. Due to its low nickel content, pyrrhotite rejection is an important step in processing of these ores. In our laboratory, various reagents were investigated for their effect on pyrrhotite depression. Among these, a combined use of triethylenetetramine and sodium metabisulphite was found highly promising.The work described in this paper has two parts. The firs part is a summary of results obtained on process samples from the pyrrhotite rejection circuit at Falconbridge’s Strathcona Mill. The second part involves simulation of the circuit performance based on the reagent conditions used in the experimental work and the concept of split factors.Two sets of reagent conditions were evaluated. The first one involved baseline conditions, simulating the current reagent performance. The second one simulated the impact these new reagents can have on the circuit performance.The simulation results obtained under baseline conditions indicated a good agreement with the current circuit performance (Figure 1). The simulation results suggest that at practically the same pentlandite recovery and tailing grades, the circuit concentrate nickel grade can be doubled through effective pyrrhotite rejection by these new reagents (Figure 2)."

Jan 1, 2003