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By V. A. Chanturiya

The state-of-the-art of mineral mining and metallurgy industry in Russia is characterized by high demand of nonferrous, rare, rare earth metals, and highgrade coal, on the one hand, and by involvement of natural and technogenic minerals with low content of valuable components, fine (nearly emulsion) dissemination of valuable components and close physicochemical and process properties. This calls for high-productive and ecology-friendly technologies for more efficient mineral beneficiation based on intensification of operating and new methods to extract valuable components from rebellious ore and technogenic minerals, relying on the last achievements of basic sciences, combination of dressing and chemico-metallurgical processes and using advanced pyro- and hydrometallurgical technologies. The transition to a new strategy of processing is only possible based on the new technological–mineralogical appraisal of a mineral raw material. Actually, the process mineralogy has a stock of modern high-resolution physical methods for analyzing composition, structure and properties of geomaterials, inclusive of micro- and nano-levels: - Identification of micro- and nano-size noble metals, and natural and induced formations on mineral surface; - Experimental validation of structural phase and chemical transformation of minerals under different energy input; - Justification of choice and mechanism of interaction between flotation agents and noble metals with complex material constitution; - Analysis of structural, phase and chemical transformations of sulfides and rocks under leaching. Thus, process mineralogy is an informational background for a unified theoretical approach to scientific justification of flowsheets of efficient mineral processing. The article gives a brief review of practices that have found application and proved to be of high economic efficiency. Such practices are: X-ray radiometry and photometry separation (Uchalinsky and Gaisky Mining and Processing Integrated Works of ALROSA); selective disintegration (equipment engineered by Mekhanobr-Tekhnika and IPKON RAS); process selectivity enhancement (IPKON RAS, Central Research Institute for Geological Exploration of Nonferrous and Noble Metals, Chinakal Institute of Mining, Siberian Branch RAS, etc.); bacterial gold leaching (Olimpiada MPIW, technologies developed the Central Research Institute for Geological Exploration of Nonferrous and Noble Metals, Nezhdaninsky deposit projects, etc.); combination processing at a mining and metallurgy plant (Norilsk Mining and Metallurgical Company, Yaregsky deposit projects and others); processing of waste: overburden, mill tailings, slag, etc. (Kovdorsky MPIW, Svyatogor JSC, Ural Mining and Metallurgical Company, plants designed by the Central Research Institute for Geological Exploration of Nonferrous and Noble Metals, Mining Institute of Kola Science Center RAS, Research Institute for Chemical Technologies); water conditioning in mineral dressing circuits (ALROSA, equipment by IPKON, etc.); utilization of process water (ALROSA, Ural Mining and Metallurgical Company, Severalmaz JSC and others). Thus, Russia this time has the academic and engineering background for development of efficient energy-saving technologies for comprehensive advanced processing in accordance with the world’s standards, or even higher in terms of a number of the technologies, which has continually been highlighted by participants of recent international congresses on mineral processing.

Jan 1, 2018

By Leopoldo Gutierrez, Esau Arinaitwe, Marek Pawlik

"The effect of various polymers, including: anionic carboxymethyl cellulose (CMC), polystyrene sulfonate (PSS), humic acids (HA) and non-ionic hydroxypropyl cellulose, on the wettability of Athabasca bitumen was evaluated through dynamic contact angle measurements using the captive bubble technique. The tests were carried out as a function of pH at a constant ionic strength (0.01 mol/L sodium chloride). The evolution of the three-phase contact angle between the solution, bitumen and an air bubble was followed as a function of time over a period of ~6 minutes. The contact angle data were modelled using a first-order kinetic equation. The results were analyzed in terms of the initial contact angle, the evolution rate constant, and the steady-state contact angle value. In the case of anionic polymers, a pronounced decrease in the initial contact angle value was observed at pH 3. Under acidic conditions, there was no significant effect of CMC observed on the steady-state contact angle value but PSS and HA significantly decreased the steady-state contact angle value. At pH 8.5. the anionic polymers did not affect the wettability of the bitumen surface but they significantly decreased the contact angle evolution rate. These results suggested that CMC is not capable of permanently lowering the hydrophobicity of bitumen, and the polymer only slowed down the evolution of the contact angle to the steady-state value. The results also showed that polystyrene sulfonate and humic acids were capable of making bitumen hydrophilic but only under acidic conditions. Only hydroxypropyl cellulose (HPC) produced a large decrease in the steady-state contact angle under alkaline conditions (pH 8.5). The kinetics of contact angle evolution in the presence of HPC was also drastically lowered. The results were discussed in terms of the chemical composition of the polymers and their different affinities towards the bitumen surface."

Jan 1, 2014

By P. Somasundaran

Gangue minerals can often have severe adverse effects on selective value mineral separation. Such effects can be mediated through a variety of pathways or mechanisms. One popular mechanism is that of ?slime coating? or heterocoagulation, wherein the gangue mineral fines are believed to coat the value mineral surfaces and thereby reduce selectivity and floatability. Another pathway that has received relatively little attention is that mediated through the effect of gangue minerals on pulp rheology, and consequently selective separation. Our recent work in developing a scientific understanding of these effects has highlighted the prevalence and importance of this pathway. In this study, the impact of shape and morphology of serpentine gangue minerals on suspension rheology and selective Ni flotation from ultramafic ores was investigated. We found strong evidence for micro- and macro-network formation in the presence of acicular (needle-shaped) or fibrous minerals, which impacted pulp rheological properties. Results also supported the hypothesis that morphology has a greater role to play than mere shape. The size of the network ranged from 5 microns to 2 cm depending upon the amount and aspect ratio of fibrous minerals. These networks impede many flotation sub-processes, such as gas dispersion and bubble-particle interactions. Additionally, the small pore size of the networks prevents bubble penetration leading to a large transport of the gangue minerals to the concentrate via lifting of the entire network by bubble flux, which resulted in a significant grade dilution. Based on the scientific insights generated in this study various techniques have been developed to improve selective value mineral separation. Keywords: fibers, aspect ratio, microstructures, networks, pulp viscosity, gangue transport

Sep 1, 2012

By J. Wiese, K. Corin, Z. Song

"Relating flotation performance to the electrochemical characteristics of a pulp is complex both in fundamental research and in practice. In the case of thiol collectors, different Eh values in the flotation system can result in the formation of the dimer or the metal thiolate which may or may not enhance the hydrophobicity of the mineral. Reducing or oxidizing conditions in a flotation system, viz. changing the Eh value, are usually manipulated to achieve an optimum flotation response by control of pH and dissolved oxygen levels in the system. A variation in pulp potential may also be achieved by the addition of potential modifiers such as sodium hydrosulphide (NaHS), sodium hypochlorite (NaClO) or hydrogen peroxide (H2O2). There exists anecdotal evidence which suggests that the addition of small amounts of H2O2 to the flotation process can improve sulphide mineral recovery. The objective of the present study was to investigate the effect of the addition of the potential modifier, H2O2, on sulphide mineral recoveries and grades in the flotation of sulphide minerals from two copper bearing ores from China and compare the results to those obtained for a PGM bearing ore South Africa. Batch flotation tests were conducted using the three different ores at the natural pH of the different systems, in the presence of a xanthate collector and the absence and presence of H2O2 as a potential modifier. The results indicate that the addition of carefully controlled low concentrations of H2O2 resulted in improvements in flotation performance. INTRODUCTIONElectrochemical potential as a control parameter in the flotation of sulphide minerals has been widely studied (Allison et al., 1972; Gardner and Woods, 1979; Ross and Van Deventer, 1985; Chander, 2003; Woods, 2003; Javadi, 2013). There is concensus that in order to be recovered during flotation, sulphide minerals require a suitable redox environment. During the flotation process thiol collectors and sulphide minerals are involved in electrochemical reactions which result in the formation of hydrophobic species at the mineral surface (Finkelstein and Goold, 1972; Rand and Woods, 1984). Sulphide minerals act as semiconductors and electrons are transferred during the interaction of the mineral with collector. The resultant potential difference and its magnitude are responsible for the transfer of electrons and the rate of the reaction (Bard and Faulkner, 2001; Fuerstenau et al., 2007). Reducing or oxidizing conditions in a flotation system, viz. changing the Eh value, may be manipulated to achieve an optimum flotation response by control of pH and dissolved oxygen levels in the system (Heyes and Trahar, 1979). The use of potential modifiers viz. reducing or oxidizing agents which include H2O2, NaClO, and NaHS, is an alternative method by which to control the potential of the pulp in a flotation system which may or may not promote the flotation of desired minerals (Rao, 2004). The oxidizing agent, H2O2, undergoes a cathodic reaction which can result in the enhanced flotation of valuable minerals. The potential of the system is increased which results in a shift in the mixed potential of a mineral. The magnitude of the over-potential influences the rate of the oxidation process and thus the flotation response of sulphide minerals (Kocabag and Guler, 2008). Equation 1 shows the proposed oxidation of xanthate by H2O2 (Lipkina and Streltysn, 1970)."

Jan 1, 2018

By A. V. Kurkov

The secondary action reagents (SAR) are organic diphilic compounds capable of altering ac-id-base and donor-acceptor properties of the main collector and consequently the energy of collector interaction with the mineral?s surface, its hardness and fixation forms ratio through associates formation via the hydrogen bonds. When the basic flotation conditions are being established, convergence of the electronic structure of the collector and the mineral being extracted due to minerals surface preconditioning with modifiers and the most efficient collector choice. At the next stage of the selective flotation condition establishment SAR is selected for a more precise adjustment of the energy of the collector fixation on the mineral. Such an approach makes it possible to solve efficiently various issues of flotation separation of non-sulfide minerals. In particular neutral organic substances containing groupings C==O, S==O, P==O (ethers of carboxylic and phosphonic acids, amides of carboxylic, phosphonic and sulfonic acids) were proposed as SAR. In order to enhance the flotation process selectivity in the conditions of water recycling including the selectivity of carboxylic collectors especially in the environment of high hardness water flotation, it was proposed to use SAR with long hydrocarbonic radical and groups with enhanced electronic density within the molecule: N-methylolamides of alkylphosphoric acids and ethers of methylphosphonic acid. Introduction of small amounts of these compounds alongside with the main fatty-acid collector enhance the performance of fatty-acid flotation of fluorite, beryl, columbite etc., lowers the collector consumption, and completely compensates the depressive effect of recycled water. Di-2-ethylhexyl ether of methylphosphonic acid?CH3P(O)(OC8H17-i)2 (hexarane) was more thoroughly researched as such an agent within fatty-acid flotation process. Following aspects of the flotation system were studied: interaction of oleic acid and sodium oleate with hexarane in the liquid phase (infrared spectroscopy); heat emission under the interaction of hexarane-oleic acid ? sodium oleate ? calcium salts (isoperiboric diathermic colorimeter); colloid-disperse state of the collector influenced by hexarane (nephelometric analysis); dynamics of the mineral surface hydration due to the agents (method of indicator negative adsorption); hexarane effect upon the interaction of fat-ty-acid collector with calcium salts (complexometric method with Trilon-B); floatability of pure minerals (quartz, microcline, beryl, columbite) in Hallimond tube; hexarane effect upon oleic acid (sodium oleate) adsorption (nephelometric method for identification of the residual content of oleic acid and its forms within the solution). Upon the research it can be definitely concluded that the adjusting effect of such compounds as hexarane within the non-sulfide minerals flotation process is mainly determined by their interaction with the main collector both within the pulp and at the mineral surface with associates formation due to the hydrogen bond. The consequence is calcium oleates destruction with the release of the most active collector under flotation in hard water environment which determines the efficiency of hexarane joint application with fatty-acid collector under recycled water supply. Therefore the introduction of the class of secondary action reagents is supported by their operation mechanisms and flotation process function and determines a new approach to the development of efficient conditions of selective flotation separation of non-sulfide minerals.

Jan 1, 2014

By Tamal K. Ghosh

In this study, the QEMSCAN technology is used to acquire quantitative modal, textural, mineral association and liberation data on different products generated from with or without washing, fractionation by size and density using screens and heavy liquids/panning, which has provided significant information on the quality and beneficiability of four categories of low Grade iron ores from Jharkhand-Orissa region. The deposit of low Grade iron ore has been categorized into four categories viz. Grade-I with <45% Fe(t) a) containing shale rich type and b) BHJ rich type; Grade-II with 45-55% Fe(t) and Grade-III with >55% Fe(t) containing conventional flaky, hard, kanga, lateritic, shale and BHJ litho/ore types in varied proportions. Mineralogy is similar across all samples being hematite, martite, goethite, kaolinite and gibbsite. Banded Hematite Jasper has difficult liberation characteristics due to highly compact banded mode of silica mineral occurrence with hematite. In all categories, the grade dilution is by the presence of 1) ?Discrete gangue rich litho types? at lump size and 2) ?Within ore types?. The second type of grade dilution contains coating of gangue phases around the iron ore minerals and different degree of locking of gangue phases within iron ore minerals. Further characterization and beneficiation assessment details are discussed in this paper.

Sep 1, 2012

By Kaiwen Liu

Activated carbon is widely used in the removal of organic and/or inorganic contaminants from waste water due to its high surface area, porous structure, and specific surface reactivity. However, in practical applications, it is difficult to recover the activated carbon completely by screening or classification. In this project,we prepared a magnetic form of activated carbon (magnetic activated carbon or M-AC) by precipitation of iron oxides on the surface of activated carbon. The M-AC can be easily separated from effluents by applying an external magnetic field, thus it can be recycled and regenerated for reuse. M-AC was characterized by X-ray diffraction (XRD), specific surface area measurement, and scanning electron microscope (SEM).XRD results show that the major phase of coated iron oxides on activated carbon is magnetite (Fe3O4). The specific surface area of activated carbon was found to be reduced after the impregnation of magnetite particles on the surface. The SEM micrograph shows the aggregation of the iron oxides on the surface of activated carbon. M-ACwas found effective in removing DETA (diethylenetriamine) species and metal ions from solutions. Cu (II) with initial concentrations from 5 ppm to25 ppm in solution is removed by more than 99% with the addition of 0.1 wt.%ofM-AC. For the removal of 25 ppm DETA species from solution, an addition of 0.5 wt.% of M-AC is required due to the larger size of the DETA molecule. Moreover, M-AC showed a good loadingproperty for nickel and gold ions from solutions. M-ACshows a better adsorption capacityover activated carbon and its potential applications in carbon-in-pulp for gold leaching and waste water treatment. Keywords: magnetic activated carbon (M-AC),diethylenetriamine (DETA),metal ion,adsorption

Sep 1, 2012

By S. Gomez, P. A. Bebswa, A. N. Mwale

"The research aimed at improving the way screen performance analysis is conducted using a model that accounts for most feed and design parameters in its formulation. Thus, the aim was to validate the fine screen model that was developed at the Centre for Minerals Research (CMR) unit at the University of Cape Town. Fine wet screening is increasingly becoming an important application in fine grinding operations. Minera Saucito, a lead-zinc Mexican mine has replaced hydrocyclones with eight stacks of five decker derrick screens to close the ball mill in their concentrator plant. The five decker stacks have improved the overall plant throughput by 20% and have had the ball mill circulating load reduced considerably. As a continuous plant optimization process, a number of surveys were carried out to assess the performance of the 75 µm panel aperture installed screens. The surveys were conducted at seven different feed rates to the entire nest of screens to collect performance data. Using the fine screen model to analyze the results, it is found that as the feed rate increase, the sharpness of separation reduces. The CMR fine screen model was fitted to these results. The model fits the plant data with good accuracy. Simulated results based on this model are also presented.INTRODUCTION The potential of high frequency vibrating screens has long been identified as an alternative to hydrocyclones in grinding applications (Rogers and Brame, 1985). However, high frequency vibrating screens have had two main disadvantages, low capacity and high wear rates (Kelley and Mckeon, 2005; Teknikk, 2009). Current vibrating screen technology overcomes these challenges by multiple deck screen design and use of wear resistant urethane materials for panel construction (Kelley, 2007; Valine and Wennen, 2002). For a example, the Derrick screen’s material of construction is a tensionable urethane that provide high open area ranging between 35 to 45% with considerably reduced blinding (Valine and Wennen, 2002). Thus, there has been an increased uptake by the mining industry in the use of wet fine vibrating screens closing the ball mill as the final classification stage in the comminution circuit (Barkhuysen et al., 2010; Frausto, Ballantyne et al. 2017; Pelevin and Lazebnaya, 2009; Teknikk, 2009). Even though there is a number of models in existence, none of these models adequately predict the performance of high frequency vibrating screens (Karra, 1979; Rogers, 1982; Subasinghe et al., 1990; Trumic and Magdalinovic, 2011). Recently Mwale et al., (2016) developed a model for predicting the performance of high frequency vibrating screens using the partition curve properties. The input parameters of the model include screen open area (??) in m2, tonnage feed rate (????) (tph) and the weight fraction of solids (??) in the feed for a given panel aperture size. The model was developed based on data collected from a single deck industrial size derrick screen, in a pilot setup. The work presented in this paper is an attempt to test this model using data collected from Minera Saucito concentrator, an industrial plant whose comminution circuit is shown in Figure."

Jan 1, 2018

By Edgar Schach, Tom Leistner, Markus Buchmann, Urs A. Peuker, Martin Rudolph, Marius Kern

"In this study, the flotation characteristics of a cassiterite-bearing fine-grained and complex skarn ore from a deposit in the Ore Mountains is investigated. The tests are performed using an oil-assisted column flotation approach to process very fine ore fractions and avoid losses of cassiterite into the tailings. First, process parameters are obtained for a finely ground artificial mixture of quartz, magnetite and cassiterite, simulating the real ore. Thereby, magnetite is used, as iron oxides can have a detrimental effect on the flotation due to a similar flotation behavior. In addition, they can act as a source of multivalent ions, which are known to reduce the concentration of collector molecules, active for flotation. Based on the results, selected parameters are further tested for cassiterite skarn ore from the Hämmerlein deposit including a pre-conditioning and a water exchange step to remove ionic contaminants. The process response is analyzed in detail by XRF (X-ray fluorescence) and MLA (mineral liberation analysis) to get a better understanding of the behavior of the single ore components. Sulfosuccinamate type surfactant is utilized as the collector, emulsifier and to reduce the froth destabilization through nonpolar oil. Sodium hexafluorosilicate is added as the depressant.INTRODUCTION Complex skarn ore deposits containing considerable amounts of tin, indium and other metals are located in the Ore Mountains region (Germany). In this study, a skarn ore from the Hämmerlein deposit was investigated. Due to the finely disseminated nature of this ore, past beneficiation attempts failed, and the ore was considered economically unprocessable. However, increasing resource demands brings it back into focus (Schuppan and Hiller, 2012). Cassiterite is the main tin bearing mineral in this ore. Due to its high density (~7 g/cm³), the predominant beneficiation technique is gravity separation (Angadi et al., 2015). Tin ores from disseminated deposits have to be extensively comminuted to reach a sufficient degree of liberation of the cassiterite grains. As cassiterite has a brittle nature, it is preferable enriched in small size fractions, during comminution (Angadi et al., 2015). Gravity separation methods become more and more inefficient for particles smaller 40 µm (Falcon, 1982), causing tin losses of up to 30 to 40wt.-% (Angadi et al., 2015). Thus, froth flotation of cassiterite was first utilized in Altenberg in the Ore Mountains as an additional processing step to reduce the cassiterite losses into gravity separation tailings (Bulatovic, 2010; Gruner and Bilsing, 1992). Although the reported lower size limits for an effective cassiterite floatability are often smaller compared to other minerals, the flotation performance is in general decreasing for small particle sizes < 10 µm (Trahar and Warren, 1976). Therefore, different approaches have been already investigated for the flotation of such fine cassiterite fractions to overcome the limits in particle size. Bilgen et al. investigated the shear flocculation of cassiterite with a sulfosuccinamate collector (Bilgen et al., 1994). The agglomeration flotation of cassiterite has been tested by Schubert et al. (Schubert et al., 1966), in which the selective coagulation of fine hydrophobic particles and oil droplets leads to an increase of the effective particle size. Recently, Leistner at al. investigated an oil-assisted agglomeration flotation for ultra-fine cassiterite ore fractions (Leistner et al., 2016). However, a poor response due to an increased concentration of Fe and Ca ions, unselective oil/gangue coagulation and froth instability, that is caused by oil/frother interactions, has been observed."

Jan 1, 2018

Spent automobile catalyst is an important secondary resource of PGMs (platinum group metals) and the recovery is significant. Various methods of recovery technology have been reported and applied in practical production, including pyro- and hydrometallurgical processes. Since the grade of PGMs in the catalysts is so low, approximately 0.5 wt. %, the present recycling technologies require high energy-consumption, it is of great significance to enrich the PGMs with some energy saving physical separation methods as a pretreatment. Automobile catalyst is usually composed of cordierite phase as a substrate and alumina phase, with PGMs, which covers the cordierite phase. We adopted the quenching pretreatment, one method of thermal shock, to generate micro-cracks between the two phases and separate the alumina phase from cordierite. Quenching was carried out by heating the catalysts in an electric furnace of different temperatures followed by rapid soaking into cold water. It was found that the phase boundary between alumina and cordierite was broken in the quenching and selective separation (detachment) of alumina from the cordierite could be achieved in the following surface grinding. The effect of quenching was checked by microscopic observation, hardness measurement, and chemical analysis. This paper figures out the stress formula of the quenching process, which is largely connected with layer thickness and temperature gradient by using an FEM (Finite Element Method) simulation and clarifies the mechanism of crack generation in the quenching process. Keywords: automobile catalyst, PGM, quenching process, FEM

Sep 1, 2012

By Valentine Chanturiya1

We have developed a classification of geochemical barriers according to their origin, i.e. natural and artificial, and according to methods and areas of application. There has been an examination of the interaction between different classes of geochemical barriers with sulfate solutions containing nickel, copper and iron. As natural barriers, carbonates (calcite and dolomites) were used. For artificial barriers, a mixture of serpentine and carbonatite, thermo-activated copper-nickel dressing tailings, and a magnesium-containing sorbent based on brucite was used. Keywords: geochemical barriers, physical-chemical geotechnologies, treatment of natural and waste water, recovery of nonferrous metals

Sep 1, 2012

By Priyanka Dhar, Kurt Aasly, Hanumantha Rao Kota, Hassan Bouzahzah, Maria Thornhill

The interest in investigating the processing characteristics of mineral deposits in Norway has seen an upsurge in the last decade. One of the major areas of interest is a huge copper deposit, operated by NUSSIR ASA located in the Repparfjord Tectonic Window in the caledonides of west Finnmark. This study reports analysis of ore from the deposit for development and modifications in the flotation flowsheet for the NUSSIR ASA copper ore. The mineralogical characterization for the ore sample was achived by optical microscopy and Zeiss automated mineralogy while grinding characteristics were tested using Bond Index tests. The results confirmed the presence of Cu minerals in the form of chalcocite, chalcopyrite and bornite in the samples, which are mainly liberated in the – 105 µm size range. The majority of non-liberated copper sulphides associated with silica and the carbonates varies from 3 to 28 percent in the –250 µm samples . It is also observed that the copper minerals are uniformly distributed in all size ranges. Selective flotation of NUSSIR copper ore was performed in different size fractions with a motive to identify the correct liberation size and thus to obtain a copper concentrate meeting the quality requirements. The flotation experiments are essentially performed in two stages: the rougher and the cleaner stage. Mass balance calculations were performed showing that approximately 88 percent of copper can be obtained at the end of the process. Ultimately, overall circuit copper recoveries ranged between 83.5 to 88.1 % with a concentrate grade of 35 to 48 % Cu.

Jan 1, 2018

By Lev Filippov, Lorène Dessalas, Inna Filippova, Yves Foucquet

"Seafloor massive sulphide (SMS) deposits, similar in composition and genesis to terrestrial volcanogenic massive sulphide deposits, are generally found in volcanic seafloor environments along major rifts and mid-ocean ridges. Theyare associated to extensional tectonic settings such as nascent-arc, rifted-arc and back-arc environments. They may represent important source of base metals and be an alternative to on-land resources. Seafloor massive sulphide deposits have particular mineralogical compositions and textural features differentiating them from terrestrial one. When extracted from salty water and exposed to the ambient air, massive sulphide samples strongly oxidize and soon become covered by thin layers of iron, copper and zinc rich sulphates and oxides, as well as elemental sulphur. The textural properties vary according to the degree of maturity and the sample position within the hydrothermal deposit. The total porosity of that type of samples is also relatively high, especially for immature samples such as black smoker chimneys, which can reach 15% of total porosity. Because the secondary mineralization and porosity level are different, seafloor massive sulphides ores respond differently from terrestrial ore to processing methods. Froth flotation, commonly applied to separate all type of sulphides from the gangue, is one possible technique for processing seafloor ore. Sulphide recovery rate is, in most cases, excellent (>90%) however separation of the various mineral phases is difficult to obtain even when applying known methods used for terrestrial ore. Moreover, the flotation behaviour decreases drastically with the time of conservation at the surface, even when the samples were stored in a confined environment. High pH values, which is a good way to depress pyrite and therefore to favour the flotation of copper and zinc sulphides, do not have the same effect on seafloor ore. Consequently, careful flotation procedure must be elaborated to obtain efficient mineral separation technique for this specific marine ores."

Jan 1, 2014

By Z. Cheng, Y. Han

"For non-sulphide minerals such as oxidized minerals, fluoride minerals, and oxysalt minerals, there are generality in the molecular structure of their floating collectors, and similarity in crystal structure of the minerals. In the paper, adsorbing mechanism of these collectors on the surface of these mineral particles in different pH pulp was investigated by means of Pauling's rules & valence bond theory, Valence-shell electron pair repulsion theory (VSEPR) theory, Crystal and ligand field theory, and quantum chemistry simulation by DMol3 and CASTEP modules of Material Studio software. Besides, the role and status of hydrogen bond in the floating adsorption mechanism were studied emphatically, and the confirmation and characterization of hydrogen bond were explored also based on the test results. What is more, the conclusion “the effect of hydrogen bond can not be overlooked in adsorbing mechanism of flotation collectors on the minerals” and a new viewpoint of multi-polarity collaboration and hydrogen bond coupling were summarized eventually based on analysis of the measurements. Finally, a novel collector 2-Amino-3-Methyl Heptyloxy-Propylamine (AMHP) was developed based on the new viewpoint of molecular structure design, and its collecting performance was exhibited.INTRODUCTIONWhen it comes to the recovery of flotation, it is necessary for researchers to investigate the flotation mechanism of collectors. In traditional theory, when collectors were used to collect minerals, the attractions between collectors and minerals were divided into chemical, electrostatic and physical attractions (Wills, B.A., 2006). Especially, because of the reaction between sulphide minerals and sulphydryl collectors is complex and various mechanism has been proposed (Yoon and Basilio, 1993), when collectors were used to collect non-sulfide minerals, it can be classified into oxyhydryl anionic collectors and cationic collectors. In traditional theory, the adsorption of oxyhydryl anionic collectors were due to water-repulsion, and the adsorption of cationic collectors were due to electrostatic attraction between the polar head of the collector and the charged electrical double layer on the mineral surface (Wills, B.A., 2006)."

Jan 1, 2018

By M. Ghiani, R. Peretti, S. di Giovanni, G. Zonnedda, A. Serci, A. Zucca

"Beneficiation of the epithermal gold mineralizations associated with an extensive alteration zone in the Serrenti-Furtei region on the island of Sardinia, is proving a complex issue. Experimental investigations have in fact demonstrated that while the ores contained in the upper parts of the deposit are amenable to conventional cyanidation, the gold contained in the refractory ores in the lower portions needs to be recovered by means of flotation, combined with leaching where necessary.The results of commercial heap leaching, carbon-in-leach (CIL) processing and flotation, designed on the basis of the experimental findings and applied to the oxidized portions and transition zones of the deep sulphide mineralizations, confirmed the expectations emerging from the laboratory tests."

Jan 1, 2003

By Gu Guohua

The alteration of surface properties of chalcopyrite after biological conditioning with Leptospirillum ferriphilum was studied by adsorption, zeta-potential, contact angle and bioleaching tests. The strains of L. ferriphilum cultured using different energy sources (either soluble ferrous ion or chalcopyrite) were used. The adhesion of bacteria to the chalcopyrite surface was a fast process. Additionally, the adsorption of substrate-grown bacteria was greater and faster than that of liquid-grown ones. The isoelectric point (IEP) of chalcopyrite moved toward that of pure L. ferriphilum after conditioning with bacteria. The chalcopyrite contact angle curves motioned diversely in the 9K culture with and without chalcopyrite powders. The results of X-ray diffraction patterns (XRD), scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS) analysis indicated that in the bioleaching process by L. ferriphilum, the surface of chalcopyrite was covered with sulfur and jarosite. Furthermore, iron phase dissolved preferentially from chalcopyrite surface during bioleaching from EDS detection. The copper extraction was low resulting from the formation of a passivation layer. The major component of the passivation layer that blocked continuous copper extraction was sulfur, not jarosite.

Sep 1, 2012

By S. M. Wen

In mineral processing, the settling of mineral particles in water, the flow of ore pulp, the dewatering and filtering of concentrates and so on, are related to the pulp viscosity. While the interaction between mineral particle surface and water affects directly the pulp viscosity. Therefore, it is of great value to the development of mineral processing theory to research the effect of mineral particle surface on the water viscosity in boundary layer. In micro-fluid, the effect of mineral particle surface on the water molecules in boundary layer can not be ignored. The water viscosity in boundary layer and the effect of the nature of mineral particle solid surface on the viscosity are analysed based on the deduction of attraction potential energy formula of mineral particle surface to the water molecules in boundary layer. The results show that the attraction potential energy of mineral particle surface to the water molecules in boundary layer is determined by the properties of solid molecules and fluid molecules and varies inversely as the third power of the distance from mineral particle surface. The water viscosity in boundary layer consists of the viscosity of free water and the additional viscosity resulting from the attraction of mineral particle surface. The increment of the viscosity caused by the attraction of mineral surface is µs. This additional viscosity is also inverse ratio to the third power of the distance from mineral particle surface. The greater the dipole moment, the polarizability and the ionization energy of mineral particle solid surface molecules are, the higher the attraction potential energy of mineral particle surface to the water molecules and the water viscosity in boundary layer are. The thicker stationary water boundary layer is d0. The higher the µs is, in other words, the greater the attraction of solid surface to water molecules is, the thicker the stationary water boundary layer becomes when free water viscosity is constant.

Jan 1, 2014

By A. K. Suri

India plans to increase the nuclear power share in overall energy-mix to about 30% by 2032 using both indigenous and imported reactor technologies. In the immediate time-frame, it is envisaged to generate 10000 MW electricity by PHWR technology by 2020 using indigenous uranium resources. This necessitates setting-up of new uranium mills and augmenting the existing resource, mining and milling capacities. This paper describes the current status and future R & D needs towards achieving the targeted demand of yellow-cake. Keywords: uranium, hydrometallurgy, leaching, yellow cake

Sep 1, 2012

By A. De1

Because of the extremely low utilization of strain energy in the breakage of solid particles, the energy efficiency prevalent in comminution technology is extremely poor. Schoenert considered that single-particle comminution under slow compression is the most energy-efficient mode of comminution and that energy efficiency should be compared to that. The usual method for grinding minerals and cement has been the ball mill, in which the hit-and-miss aspect of loose-bed comminution severely reduces energy efficiency. The fine grinding of minerals is a particularly energy-intensive process. Schoenert showed that the energy consumed in the comminution of particles in confined beds is second only to that of single-particle comminution under slow compression and developed the method of conducting particle-bed comminution continuously in a high-pressure roll mill. Since its first industrial installation in 1985, the high-pressure roll mill has established itself as the comminution device of choice for significantly improving the productivity and energy efficiency of size reduction from coarse size feeds down to products finer than 20 microns. The first of several hundred installations were in cement plants. The preliminary design and optimization of the industrial operation of high-pressure grinding roll (HPGR) systems, owing to the continuous nature of the device, cannot be efficiently done through laboratory experiments and needs to be achieved through proper system modeling. While the energetics of size reduction in high-pressure grinding rolls has been modeled very well, no model exists for the macroscopic variables in HPGR comminution. In high-pressure roll mill grinding, size reduction results from confined particle-bed comminution under compressive stresses such that the daughter particles produced are highly fractured, stressed, or otherwise weakened. This paper attempts to relate the comminution / compaction behavior for confined particle-bed under compression in a piston-die press with the macroscopic variables in HPGR comminution. A model describing the pressure-densification relationship is presented and used to accurately simulate the macroscopic variables in high-pressure grinding rolls, utilizing experimental data for particle-bed comminution with the piston-die press. The accuracy of the predictive simulations strongly suggests that, starting with a few batch-mode laboratory-scale experiments, it should be possible not only to identify the optimal operating conditions for existing operations but also to successfully design new industrial high- pressure grinding roll systems.

Sep 1, 2012

By Zhong Hong

A novel ilmenite collector, tert-butyl benzoic hydroxamic acid (TBHA), was investigated in this paper. The flotation performance and adsorption mechanism of TBHA to ilmenite were evaluated through pure mineral flotation tests, ?-potential measurement and IR spectrum analysis. The experiment results indicated that TBHA exhibited strong collecting capability to ilmenite under pH 6.0-8.5. At pH 7.0-10.0, TBHA existed in the form of anionic species in aqueous solution, and the ?-potential measurement results showed the surface of ilmenite maintained negative and more negative after the adsorption TBHA on it, which inferred that TBHA might adsorb on the surface of ilmenite through chemical interaction. The IR spectrum analysis further confirmed the chemical interaction between TBHA and ilmenite surface. Keywords: Tert-butyl benzoic hydroxamic acid, Ilmenite, Flotation, Chemical adsorption mechanism

Sep 1, 2012