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By Nina Panteleeva, Elena Afonina, Stanislav Titkov, Jury Buksha

"Flotation processing of water-soluble minerals (potassium ores, sedimentary salts of salt lakes) is currently the main method for production of potassium fertilizers and concentrated carnallite which is the initial product for production of metallic magnesium. Flotation of sylvite (KCl) and halite (NaCl) is carried out in the electrolyte solutions: KCl-NaCl-H2O and KCl-NaCl-MgCl2-H2O. The report presents the results of studies of the effect of concentration and the electrolyte type on the size of air bubbles in a flotation cell in comparison with the floatability of mineral constituents of potash ores. The floatability in electrolytes of various compositions has been studied: - of sylvite (KCl) by alkylamines, - of halite (NaCl) by alkylmorpholines, - of silicate-carbonate slimes contained in the ore by ethoxylated surfactants. The reagent modes (regimes) activating the flotation desliming of potash ores have been developed."

Jan 1, 2014

By Aysan Molaei, Kristian Waters

Solvent extraction is the one of the most common techniques for recovering metal ions from aqueous systems. However, solvent extraction is generally limited to relatively high concentrations and requires a high organic/aqueous ratio. Predispersed solvent extraction (PDSE) is a modified solvent extraction technique in which organic phase pre-comminute into colloidal liquid aphrons (CLAs). In this study, the extraction of copper by the PDSE technique was investigated. The main focus of this study was on the characterization and application of CLAs under different operational conditions, and to investigate the effects of different parameters on the extraction of copper from dilute streams. The effect of phase volume ratio (PVR), initial extractant concentration and initial copper concentration was studied and optimum conditions for copper removal using CLAs generated by LIX 984N as extractant, oil soluble and water soluble surfactants were proposed. Experimental observations indicated that PVR and initial LIX 984N concentrations had a significant effect on copper extraction.

Jan 1, 2014

By Stoyan Groudev

Two experimental plots consisting of a slightly acidic soil heavily contaminated with radionuclides (mainly uranium and radium) and non-ferrous metals (mainly copper, zinc, and cadmium) were treated in situ under real field conditions using the activity of some representatives of the indigenous soil microflora. This activity was enhanced by suitable changes in the levels of some essential environmental factors such as pH and water, oxygen and nutrient contents of the soil. The treatment was connected with solubilization and removal of the contaminants from the top soil layer (horizon A) due to the joint action of the soil microorganisms (mainly acidophilic chemolithotrophic bacteria) and leach solutions (diluted sulphuric acid) used to irrigate the soil. In one of the plots, the dissolved contaminants were removed from the soil profile through the drainage soil effluents and were subjected to cleaning by a constructed wetland located near this plot. In the other plot, the dissolved contaminants were transferred to the deeply located soil subhorizon B2 where they were precipitated as the relevant insoluble forms (uranium as uraninite, and the non-ferrous metals as the relevant sulphides) as a result of the activity of the sulphate-reducing bacteria inhabiting this soil subhorizon. This activity was enhanced by injecting water solutions of acetate, lactate, ammonium, and phosphate ions to this soil subhorizon.

Sep 1, 2012

By N. Kgabi, F. B. Waanders, E. Vinken, A. Mans

"Mössbauer and SEM identification of the iron mineral phases present in South African coal fractions from the Free State, Gauteng, Mmpumalanga, Natal and Waterberg coal fields, as well as from ash samples from coal used in the Lethabo power plant, containing a large amount of inorganic matter, was conducted. The iron is mainly associated with sulphur in the mineral but the amounts of these and other minerals vary considerably in coals from diverse origins. By means of Mössbauer analyses the iron bearing minerals were identified as pyrite, jarosite, illite and ankerite. In the SEM analyses quartz, associated with various clay minerals was identified with differences in abundance found between the coals from the different locations.The fly ash, produced at the high combustion temperatures in the power plant, gave rise to a spectrum, typical of a glass. SEM analyses showed that agglo- meration of the fly ash was due to the presence of Ca in the coal. The lab. produced fly ash was combusted at temperatures ranging from 200-1 200°C and the pyrite changed partially to hematite and partly into the glass due to the presence of the quarts and the clay minerals. A similar spectrum as the power plant fly ash spectrum was obtained.In the weathering experiments the pyrite changed to a sulphate component in a very short time during air drying."

Jan 1, 2003

By Yizhong Yuan, Dao Li, Nannan Xue, Tao Liu, Yimin Zhang

A new multi-stage counter-current circulation leaching process for extracting vanadium from stone coal was proposed, and the main factors on multi-stage counter-current circulation acid leaching process were investigated. The results show that the vanadium recovery could reach 86% under the conditions of sulfuric acid concentration of 4 M, liquid to solid ratio of 2 mL/g, temperature of 95 °C, reaction time of 60 min, mean particle size of 125 µm and circulation acid leaching stage of three. The losses of vanadium in acid leaching solution appeared during the four-stage acid leaching process. The strong adsorption performance of new formed KAl(SO4)2(H2O)12 crystal was main reason.

Jan 1, 2014

By Wei Zhang, Jinhong Zhang

"In froth flotation, the adsorption of collector on mineral surface is critical for a successful flotation process. In present work, an atomic force microscopy (AFM) has been applied to study the adsorption of potassium amyl xanthate (PAX) on copper sulfides, i.e., chalcopyrite, chalcocite and bornite. The in-situ collected AFM images show that PAX adsorbs on chalcopyrite mainly in the form of oily dixanthogen; while it strongly adsorbs on chalcocite and bornite in the form of insoluble metal xanthate, which binds strongly with the mineral surface. The information obtained from the AFM study shed lights on the collectivity and therefore the selection of specific collector for different copper sulfide minerals in industrial practice.INTRODUCTIONFroth flotation, which treats the highest throughput in mining industry and produces the maximum economic outcome of any surface chemistry process, has been widely applied for the concentration of copper sulfide minerals, i.e., chalcopyrite, chalcocite and bornite. In flotation, collectors are added into the pulp (mixture of water and fine-grained minerals) to selectively adsorb onto the target mineral and render its surface with high hydrophobicity, which is generally beneficial for a strong mineral-bubble attachment and thus a high flotation recovery. Therefore, the adsorption of collector on mineral surface is vital for a successful flotation process and it has been studied by applying various surface analysis techniques, such as IR (Infrared Spectroscopy), CV (Cyclic Voltammetry) and XPS (X-ray Photoelectron Spectroscopy). (Poling, 1963; Allison et al., 1972; Mielczarski et al., 1984; Leppinen et al., 1989; Kartio et al., 1996) These studies have revealed a lot of information, such as the reaction, product and mechanism, of the adsorption of chemicals on mineral surface. It is also of great interest to directly get the image of adsorbed collectors on mineral surface changing with pulp chemistry, such as pH, redox potential, ionic strength and chemical’s dosage."

Jan 1, 2018

By S. Castro, L. Uribe

Seawater can be considered as a particular process water with a high concentration of NaCl (about 0.5- 0.6 mole/L) and high concentration of hydrolyzing metal cations (mainly, Mg2+ and Ca2+ ions). Micro-flotation tests, induction time measurements, and zeta potential measurements have been used to investigate the effect of these ions on the natural floatability of molybdenite. The results demonstrate that molybdenite is strongly depressed in the alkaline pH range over which hydrolysis products of Mg2+ and Ca2+ ions are formed. At pH 10, colloidal magnesium hydroxide seems to be responsible for molybdenite depression in seawater and in Mg2+ solutions. This is also supported by the measurements of the effect of Mg2+ ions on the zeta potential of molybdenite. The mechanism of depression of molybdenite with Ca2+ ions is different, and depression takes place in the pH range were Ca(OH)+ complexes are formed, below the pH of precipitation of calcium hydroxide. Adsorption of the cationic hydroxy species and/or hetero-coagulation of the positive charged colloidal hydroxide on the negative charged molybdenite particles seem to be the main mechanisms involved.

Jan 1, 2014

By M. Wierink

The lifecycle of a resource, specifically a metal, is often depicted as circle from primary production from mining to minerals processing and via manufacturing and use to disposal and recycling. When a material is recycled, it is considered as saved energy compared to producing the material from primary source. This is, however, a simplified representation. At each step of the life cycle, there are changes in the quality of the material due to different materials chemical and physical interaction, phase transformations due to diffusion, radiation etc. Due to these physical and chemical phenomena there are losses of material, which as determined by thermodynamics are not recoverable within the life cycle. This can be considered as an increase embodied energy per mass unit of substance and loss exergy from the material cycle. With low cyclic loss, the material will remain in the recycling loop for a long time, while with high cyclic loss it will disappear fast. Where you put the material determines how fast it disappears from the resource cycle. In this research paper the phenomena of quality degradation of material and idea of increase of embodied energy and exergy loss within a resource cycles is portrayed. The cyclic nature of material states and transitions and energy consequences of material quality degradation as well as the parameters affecting the length of the time scales of the material cycles are described. Currently the cyclic embedded energy and the history of material is not taken under consideration in generic life cycle assessment. This easily results into a conclusion that lifetime of product is optimized only in terms of how much energy an appliance uses during its lifetime, while ignoring the loss of embedded energy due to the effects caused by the environs the material is subjected to during the cycle. Better description of the time properties of material give us a possibility to design toward optimum lifetime of products in terms of resource efficiency. Keywords: product lifetime, material lifetime, recycling, cyclic resource efficiency, material state, material quality, exergy, embodied energy

Sep 1, 2012

By Ghislain Bournival, Seher Ata, Graeme J. Jameson

A common method to prevent bubbles from coalescing in a flotation cell is by the addition of surfactants, called frothers. The gas dispersion properties in a column were tested for solutions of 1-pentanol, tri(propylene glycol) methyl ether, and poly(propylene glycol) in the presence of sodium chloride. The dependency of surfactant on the gas holdup can be divided into regions. It seemed that for a sufficiently low concentration of surfactant, even a stronger surfactant could show a transition in gas holdup from constant/decreasing to increasing with concentration. This region, however, was not marked by a decrease in the average bubble size. In addition, PPG gave higher gas holdup values while averaging larger bubbles. On the other hand, sodium chloride mostly affected the gas holdup when the concentration was high enough to prevent bubble coalescence. Another parameter affecting the gas holdup was the superficial gas velocity. A linear dependency was found between the two under a bubbly flow regime. The current study showed that both surfactants and salt could slightly affect the influence of the superficial gas velocity on the gas holdup.

Jan 1, 2014

By Yuri Yemelianov, Stanislav Balikov, Alexander Epiforov, Andrey Boldyrev, Andrey Bogorodsky

"Test work was carried out using copper gold-bearing flotation concentrate with 6.85%Cu, 14.30%Fe, 20.70%S and 2.34%As. Gold and silver grade in the concentrate is 54.6 g/t and 92 g/t, respectively. Gold and copper are valuable components in the concentrate. Gold is partially associated with pyrite and fahlores. Copper in the concentrate can be found as tennantite (Cu12As4S13). The 71% of gold from the flotation concentrate is recoverable by cyanidation with simultaneous cyanide consumption in the amount of 96 kg/t. The major reason of refractoriness is that gold is fine encapsulated into sulfides and the presence of cyanicide-copper. The concentrate ground as much as 95% minus 10 µm was treated using low-temperature POX at the temperature of 100±5°C, L:S ratio of 5:1 and the process time of 1-5 hours. Residual sulfide sulfur in the cake is 2.28% which is 89% sulfide oxidation. The highest copper recovery to POX solution is 91%. It was found that gold recovery to cyanide solution is 85-94% during alkaline pre-treatment of POX cakes followed by cyanidation. In this case, cyanide and lime consumption is 75-90 kg/t and 120 kg/t, respectively. In order to recover precious metals from POX cakes leaching using sodium sulfite was carried out. Test work was conducted at varied reagent concentration, L:S ratio and leaching time. Gold and silver recovery achieved was 85-95% and 59-63%, respectively."

Jan 1, 2014

Froth flotation is an industrial process commonly used for the separation of mineral particles. Bubbles sparged in a pulp collect and carry hydrophobic particles to the top layer of a flotation cell, the froth zone. There is a strong correlation between the stability of the froth phase and the flux of solids. However, flotation units placed in series operate, as a whole, in a non-steady state regime with the concentration of particle decreasing from one cell to the next resulting in a decrease in froth stability, which can compromise the recovery of valuables. Organic chemical reagents, frothers, are generally added to prevent fine bubbles from coalescing and to increase the stability of the froth phase. Frothers represent the second largest group of mining chemicals. It is crucial to understand the resulting properties of the frother on the froth phase in order to select the most suitable reagent for a particular operation. The bubble coalescence dynamic of three different surfactants, 1-pentanol, poly (propylene glycol), and tri (propylene glycol) methyl ether, were investigated in this study. In the first stage, the stabilisation mechanism of bubbles in a solution of surfactant was investigated using a specifically designed experimental setup. The coalescence behaviour of bubble pairs was recorded using high-speed video imaging in which information such as the coalescence time and the deformation of the resultant bubble upon coalescence could be extracted. The results were then compared between the different surfactants for several concentrations. It is shown in a study that the coalescence time increases with surfactant concentration until the Gibbs-Marangoni effect is suppressed by bulk diffusion. Conversely, the oscillation of the resultant bubble was found to be affected only at concentrations at which the film is saturated. The implications of the effects of surfactant type and concentration on the coalescence time and bubble oscillation in froth flotation are discussed. Keywords: froth flotation, frother, bubble coalescence

Sep 1, 2012

By S. A. Vorobyev, Yu. L. Mikhlin, Ye. V. Tomashevich, A. A. Karacharov, M. N. Likhatski1, A. S. Romanchenko, S. V. Saikova

"A set of state-of-the-art methods have been applied to study ultrafine particles and nanoscale species arising on mineral surfaces upon milling, interaction with flotation reagents, and leaching of base metal sulfide ores in order to gain insights into interfacial mechanisms. The fine fractions produced by ball milling of a Pb-Zn Gorevsky ore and four Cu-Ni sulfide ores studied with laser diffraction, dynamic light scattering, zeta-potential measurement, Xray photoelectron spectroscopy (XPS), SEM, TEM and other techniques. The particle size distributions had, aside from the peaks at 20-60 ?m, maxima near 1-2 ?m; the flotation was considerably suppressed when the yield of positively charged ultrafine particles approached tenths % (several kg per ton). High-energy XPS and X-ray absorption spectra revealed that sulfide minerals depleted in metal in air and aqueous solutions were composed of outer “polysulfide” layers, strata with disulfide species, and heavily defective underlayers, and “passivation” was explained by stability of the metal-deficit structures. Dixanthogen at pyrite and copper-activated sphalerite, dixanthogen and then cuprous xanthate on chalcopyrite, and chemisorbed xanthate at galena were specified as the main interfacial products using cryo-XPS of fast-frozen flotation slurries. The particle size, zeta-potential and behavior of colloids of Cu and Pb xanthates and dixanthogens were largely determined by the initial ratio of a cation and collector; the properties of copper xanthate nanoparticles were also affected by incorporated dixanthogen (about 15 wt.%). Submicrometer gas domains of 3-8 nm in height and “hydrophobic” forces upon the probe retraction were found on xanthate-treated minerals using atomic force microscopy and spectroscopy; their impact on flotation is briefly discussed.INTRODUCTIONInterfacial phenomena play a key role in flotation, leaching, water purification and related environmental processes. The mineral processing and extraction of metal from sulfide ores commonly involves milling the ore, which produces, along with the particles of 20 µm to 100 µm, mineral entities ranging from micrometer to submicrometer and nanometer scale. Furthermore, ultrafine particles of flotation reagents, products of metal sulfide oxidation, and so on may form spontaneously and accumulate in production water, flotation froth, deposit on mineral surfaces, affecting the flotation performance, and then enter waste waters, mine and natural drainage, polluting soils, surface- and ground waters (Miettinen et al., 2010; Wang et al., 2014). The efficiency of flotation and hydrometallurgical recovery of values, environmental issues are crucially dependent on the state of mineral surfaces. Particularly, it is generally accepted that the surface non-stoichiometry of sulfide minerals induced by oxidation and leaching should affect their hydrophobicity and reactivity, including so-called “passivation”, but the nature of such surface layers are still a matter of controversy (see, for example, Holmes and Crundwell, 2013). Another phenomenon attracting rapidly growing interest in several areas is low-dimensional gas species (“nanobubbles”) at hydrophobic surfaces that may play a decisive role in particle-bubble attachment in flotation but remains scarcely investigated up to now (Xing et al., 2017). Here, we survey our recent results on the abovementioned problems applying a series of rather new methods and approaches; more details can be found in refs. Karacharov et al., 2016; Mikhlin et al., 2015; 2016; 2016a; 2016b; 2016c; 2016d; 2017; 2017a; Vorobyev et al., 2017."

Jan 1, 2018

By V. A. Ivanova, T. N. Perunkova, N. O. Dorozhanova, G. V. Mitrofanova

"Oxyethylated compounds are used as reagents-regulators in the flotation of non-sulfide ores, in particular, apatite-containing ores. Thus, the necessary degree of selectivity in the flotation separation of two calcium-containing minerals of apatite and calcite is achieved only by using, in addition to a collector, regulators-reagents from the nonylphenol ethoxylates class. In order to establish the most optimal structures, this paper presents a comparative assessment of the physical-chemical and flotation properties of several classes of oxyethylated compounds - alkylphenol ethoxylates, aliphatic alcohol ethoxylates and oxyethylated carboxylic acid. The authors have studied their dispergating ability with respect to the air phase and calcium soaps of the carboxylic collector. Dependences of foaming properties of regulators on the degree of oxyethylation have been determined. Adsorption isotherms of sodium oleate on apatite and calcite in the presence of regulators have been obtained. It has been shown that the presence of oxyethylated compounds in the solution reduces the amount of the adsorbed fatty acid collector. The influence of the considered classes of regulators on apatite flotation has been studied. The interrelation of flotation properties of oxyethylated compounds and their molecular structure has been established.INTRODUCTION Flotation plays a leading role in complex apatite-containing ores processing. However, two calcium-containing minerals - apatite and calcite, which compose apatite-carbonate ores, are characterized by close flotation properties. Selective separation of these minerals is a difficult task, the solution of which is impossible without using reagents-regulators. One of the ways to ensure the selectivity of the flotation separation of calcium-containing minerals is the use of reagents-depressants such as sodium silicate, starch, cellulose derivatives, and others (Liu et al., 2016; Rao et al., 1989). Another method is the application of nonionic reagent regulators (Filippov et al., 2016; Filippova et al., 2014; Ignatkina, 2017), which contribute to the adsorption of the ion collector (Filippov and Filipova, 2006 Rao and Forssberg, 1997) and stability of formed froth (Sis and Chander, 2003)."

Jan 1, 2018

By E. A. Bekchurina, Yu. P. Morozov

"This paper presents the results of a study of the concentration of flotation froths in tapered chutes. The tests were conducted on lab and full-scale plants, and the results obtained were mathematically processed. The kinetics of monophase recovery from a stationary flotation froth, hydrodynamics of froth flows traveling in a tapered chute were investigated. The effect was studied of the mass fraction of the valuable component in the chute feed, yield of the chute’s overflow, and chute design on the concentration performance. Processing of the collected data revealed the general laws of the process and allowed to develop a technique for modeling concentration of the flotation froths of sulphide copper ore in a tapered chute to predict the performance without testing. It was found that concentration in tapered chutes allows to obtain products that are comparable in quality with froths after one or several cleaner flotation stages.INTRODUCTIONThe present production expansion rates require continuous improvement in the grade of flotation concentrates, while the grade of the mineral feed is constantly deteriorating. This leads to a significant complication of flotation flowcharts. Flowcharts become multi-staged with multiple cleaner flotations, negatively affecting the production costs.In recent years, researchers are paying close attention to the processes occurring in the froth layer in the flotation cells. Improving the concentrate grade is facilitated by secondary concentration of minerals in the froth layer, which consists in fixing the hydrophobic particles released as a result of the coalescence of the bubbles of the upper layer when moving downward at the liquid-gas interface of the froth layer. In this case, the released hydrophilic particles, trapped in the froth layer as a result of mechanical removal, migrate from the froth together with the liquid phase."

Jan 1, 2018

By M. Canbazoglu

In this study, optimum sulphuric acid leaching parameters of zinc and other valuable metals from two different waelz clinker samples were researched. Origins of the samples are electric arc furnace dust and original non-sulphite zinc ore waelz clinkers. The main zinc mineral determined as zincite in these samples. Collective dissolution of zinc and other valuable metals in waelz clinkers can easily achieved by sulphuric acid leaching of them. 96% of zinc can be dissolved at 80 ºC, 60 g/L sulphuric acid concentration, 60 min. leaching time and 1/5 solid/liquid ratio. Almost 90% of Cd, Cu and Co in clinker dissolved at these conditions while dissolution of Fe was almost 20%. The consumed acid amount for dissolved per ton of zinc is approximately 1.7 tons at these conditions.

Jan 1, 2014

By P. K. N. Raghavan

Bauxite is the principal source for the production of aluminum metal which has gained tremendous importance over the years due to its versatility as a metal capable of substituting almost all of the non-ferrous metals, non metals like wood, plastics, fibre glass, etc. and even steel in many applications. 90% of the high purity alumina needed for the production of this wonder metal in the world comes from bauxite. Even though alternate methods have been developed to produce alumina from non bauxite sources, owing to the high capital and operating costs involved, Bayer process still retains the superiority among all the methods by virtue of its simplicity and favourable economics. Bauxite continues to be the perfect ore for alumina production and its remarkable utilization makes it the most important non-ferrous ore. Most of the Alumina Refineries in the world process different types of bauxite and that too from varied sources. The technology employed in the Alumina Refineries depends on the Bauxite processed, with an ultimate view to produce alumina of required quality in the most efficient manner. Bureau of Indian Standards (BIS) and Indian Bureau of Mines (IBM) had from time to time put forward bauxite specifications for metallurgical and other applications. However, these are found no fully based on alumina technology, present developments and availability of different types of bauxite in the country. The aim of this paper is to provide scheme of metallurgical grading of Indian Bauxite based on the background of alumina processing technologies and availability of various types of bauxite in the country. Efforts are made here to evaluate beneficiation techniques for central Indian Bauxite from the point of view of alumina production. Keywords: bauxite beneficiation, digestion, alumina, gibbsite, bohemite, diaspore

Sep 1, 2012

With significant increase in steel output in the world the price of iron ores has been soaring recently. Especially, there is a strong demand for iron ores in China, leading to more attentions paid to developing low grade iron ores. In this paper mineralogy of nm-of-mine hematite ore was deter-mined, and coal-based direct reduction-magnetic concentration was successfully developed to beneficiate low grade hematite ore. Mineralogy analysis indicates that this hematite ore is a super fine refractory ore, with the main valuable mineral hematite being closely associated with quartz and distributing uniformly and mostly occurring within the size of 3~5J.lITI,leading to being difficult to beneficiate due to super fine hematite and only grading 28.83% Fetotal. This hematite ore failed to be effectively upgraded by traditional processes in trial tests, such as reverse flotation, gravity concentration, and magnetic separation, or the integration of the above processes. In contrast with adoption of the coal-based direct reduction-magnetic separation process, concentrate was produced with high iron grade and metallization degree in the present work, which provides a theoretical basis for utilization of low grade iron ores. By optimization of direct reduction conditions, such as reduction temperatures, duration and mass ratio of reductant coal to iron ore, the reduced ore with 93.72% metallization degree was prepared, and then three-stage grinding-magnetic separation of the reduced ore were conducted, the final concentrate was manufactured, assaying 69.54% Fetotal and 98.01 % metallization degree, and with low content of impurities. This iron concentrate with high metallization degree produced by this process is a superior burden for converter instead of blast furnace. This process is enviromnent friendly by directly making iron using coal and iron ores instead of coke, resulting in less emissions and low production cost.

Jan 1, 2014

By Tamara Matveyeva, Tatiana Ivanova, Nadezhda Gromova

"The paper presents the results of study of the sorption and flotation properties of the reagents of plant origin - tannin and natural extracts of the oak bark and stems of plants, with a view to their application as a low-cost environmentally friendly modifiers of iron sulfide flotation for the recovery of minerals containing precious metals. The technique of preparation of plant extracts with a fixed content of extractable tannins has been developed.The mechanism of flotation reaction of tannin extracts has been identified as based on their adsorption on the surface of pyrrhotite and arsenopyrite to form strong complexes with iron (III) at concentrations below micelle concentration. It has been found that adsorption of plant extracts occurs without displacement of primarily adsorbed xanthate, and preliminary adsorption of xanthate did not preclude fixation of tannin on the mineral surface.It has been shown that plant extracts having hydrophilizing properties at low concentrations could be applied as selective depressants for pyrite, pyrrhotite and arsenopyrite in a weakly acidic, neutral or weakly alkaline medium. The use of plant modifiers could help to increase the quality of gold- and platinumcontaining concentrates and reduce the ecological impact on the environment."

Jan 1, 2014

By Elzbieta Mielczarski, Jerzy Mielczarski, Jan Drzymala, Yann Duval

"The monoalkyl ethers of polyethylene glycols are universal flotation reagents because they can be used as collectors, frothers, surfactants, and depressants. Their collecting power was demonstrated for different minerals including coal and quartz.It was confirmed in this work that monoalkyl ethers of polyethylene glycols could be used as collector in flotation of quartz in a monobubble Hallimond cell. Since feldspar does not float in the same cell, it was also shown that selective separation of quartz and feldspar in the Hallimond tube is possible. However, a trail to use the monoalkyl ethers of polyethylene glycols compounds for separation of quartz and feldspar by flotation of mixture of these minerals in a Mechanobr laboratory flotation machine was futile, indicating that these reagents required special environment for flotation.Most probable parameter responsible for a decrease in quartz flotation in the flotation machine is the hydrodynamics of process, and different adsorption/desorption conditions. To prove this, another series of experiments was carried out to separate quartz and feldspar, in which a laboratory flotation column was utilized. The performance of the flotation column was in between that of in the Hallimond tube and flotation machine. These experiments confirmed that the hydrodynamics of flotation plays a vital role in flotation of quartz with monoalkyl ethers of polyethylene glycol compounds."

Jan 1, 2003

By Ataollah Nosrati

Agglomeration of fine mineral particles is an important step in heap leaching processes employed for a cost-effective hydrometallurgical extraction of value metals from low-grade ores. In this study, the effect of acidic binder composition and feed ore particle size on binder dosage requirement and isothermal, batch agglomeration behavior of siliceous goethite nickel laterite has been investigated. Agglomeration tests performed with tap water and 30, 44 and 98% w/w H2SO4 solutions as binders revealed the key role of binder formulation in controlling ore particle wettability, nucleation and granule growth behavior. Both lower binder acid content and higher dosage led to greater wetting, nucleation and granule growth rates. Variation of feed ore fine/coarse particles? mass ratio dramatically impacted on binder dosage requirement for effective particle wetting, nucleation, and growth agglomeration behavior. Increasing fine (-150 µm) fraction mass content in a -2 mm feed ore, led to higher binder dosage requirement and enhanced nucleation, however the overall agglomeration rate/granule size growth decreased. In contrast, the presence of coarse (5 ? 15 mm) particles in feed ore led to (i) lower binder dosage requirement, (ii) enhanced initial agglomerate size growth rate, and (iii) reduced coalescence. For dry agglomerates of similar sizes, competent coarser feed particles led to remarkably higher compressive strength than did finer feed particles. Microstructure analyses indicated that the granules containing coarser particles exhibited a distinctive, competent core/shell (fines) structure which led to their structural reinforcement. The appropriation of the findings for optimizing agglomeration behavior for enhanced heap leaching of complex, low grade laterite ores are discussed in this context.

Sep 1, 2012