Search Documents

By A. Mainza, H. Hill, L. S. Bbosa

"Impact breakage is the most elementary size reduction mechanism in comminution devices. In comminution research, characterization of breakage is primarily concerned with the energy expended to cause it. The main challenges of this approach have been quantifying the actual energy requirements of impact breakage and developing mechanistic models to accurately describe the process. For engineering load analysis, fracture is characterized in terms of strengths such as yield stress and ultimate tensile stress, which govern the maximum loads specific materials can be subjected to before irreversible inelastic deformation and subsequently complete fracture occur. With this approach, the main challenge has been to elucidate the underlying mechanism, in the means that the load causes weaknesses in the material microstructure to act as sites for stress concentrations, leading to crack initiation, propagation and eventual failure. Studies dedicated to investigating particle fracture under impact loading have led to the development of several devices for conducting breakage characterization tests. These devices include the drop weight tester, split Hopkinson pressure bar, rotary breakage tester and the short impact load cell. All these have different particle loading and breakage methods, and thus can yield distinct information which can be compiled together to study a material and the nature of breakage. This work analyses the single impact breakage data obtained across the listed devices. A homogenous ore commonly known as blue stone is used for all breakage tests. The work is conducted using standard procedures specific to each device as closely as possible. Drop weight and rotary breakage tests were used to obtain hardness parameters based on an existing t10 breakage model, while split Hopkinson pressure bar and short impact load cell measurements provided properties based on conventional engineering load analysis. The results were used to highlight the significance of the loading geometry, impact mechanism and impulse on the extent of breakage."

Jan 1, 2018

Electrochemical behaviors of synthetic and natural enargite in buffer solutions have been investigated using open circuit potential, stationary polarization and cyclic voltammetry as functions of solution pH, scan direction, scan range, scan rate and dissolved O2. The results indicate that the electrochemical behaviors of synthetic and natural enargite are very similar; solution pH, scan direction, scan range and scan rate have remarkable effects on the electrochemical behavior of enargite while dissolved O2 has little effect on the electrochemical behavior of enargite. The potential range in which enargite possesses the ability of passivation is from ?0.9 V to + 0.83 V vs. SCE. Enargite is most stable in neutral and alkaline solution around potential ?0.2 V vs. SCE. The main oxidation products on enargite surface in alkaline solution are Cu(OH)2 while the potential imposed on it is within the range of ?0.2 V to 0.33 V vs. SCE and Cu(OH)2 + S0while the potential applied is higher than 0.52 V vs. SCE.

Jan 1, 2014

By Chanki Jeong, Heechan Cho

In this study, batch flotation experiments were conducted to recover rare earth elements (REE) from an REE ore deposit in the Mushgai Khudag area, Mongolia. Apatite was found to be the major REE mineral while monazite and xenomite were observed as minor minerals. The main purpose was to float apatite to increase the REE content. Oleic acid was used as collector and MIBC was used as frother. Sodium silicate was used as a depressant for iron compounds. NaOH was used to adjust the pH of the flotation to about 9.5~10.0. The particle size was 90% less than 152 ?m (- 100 mesh). The content of REE elements was analysed by ICP - OES to determine the contents of REE such as Ce, La, Nd, Pr and Y. When sodium silicate was used, the best result was obtained using 0.2 mL of sodium silicate, 2 mL of oleic acid and 2 mL of MIBC. Under these conditions, the recovery of REE was about 78% and the grade of the first froth product was 42,995 ppm Ce, 24,088 ppm La, 14,236 ppm Nd, 4,388 ppm Pr and 1,570 ppm Y. When conducting flotation after iron minerals were removed by magnetic separation, a better result was obtained; with 2 mL of oleic acid, 2 mL of MIBC and no sodium silicate, the recovery was increased to 90% and the grade was also increased to 58,600 ppm Ce, 28,624 ppm La, 17,160 ppm Nd, 5,348 ppm Pr and 1,971 ppm Y.

Jan 1, 2014

By Hajime Miki, Gde Pandhe Wisnu Suyantara, Tsuyoshi Hirajima, Keiko Sasaki

"Hydrogen peroxide (H2O2) is frequently used as an oxidizing agent in various applications. It has also been reported to reduce the recovery of sulfide minerals. Moreover, the previous work applied H2O2 aqueous solution in selective flotation of chalcopyrite and molybdenite. However, the oxidation method suffered in pilot scale test due to too long conditioning time. Furthermore, the excessive reagent consumption increased the reagent cost, causing the method not economically feasible. Consequently, further improvement is required to reduce the conditioning time and the reagent consumption. The oxidation performance of H2O2 can be improved by using ferrous iron as catalyst, producing a Fenton’s reagent which is more powerful oxidizer than the H2O2 itself. Therefore, the effect of Fenton’s reagent on the floatability of chalcopyrite and molybdenite was investigated in this study. The flotation test results show that selective flotation of chalcopyrite and molybdenite might be possible at low concentration of H2O2 aqueous solution by adding ferrous iron. Moreover, the conditioning time could be shortened by this improvement. To understand the phenomenon, surface characterization using atomic force microscopy (AFM) along with x-ray photoelectron spectroscopy (XPS) analysis were carried out. The AFM images show that the surface of chalcopyrite was readily covered with mountainous features which alters its hydrophobicity after the oxidation treatment. Meanwhile, the molybdenite surface remained clean and relatively hydrophobic. The XPS results indicate that the mountainous features are various oxidation products (i.e., FeOOH, Fe2(SO4)3, CuO, Cu(OH)2). Possible mechanisms of this phenomenon were proposed in this work.INTRODUCTIONConventionally, copper and molybdenum ores are separated in selective flotation circuits by using copper depressants (i.e., sodium hydrosulfide (NaHS), sodium sulfide (Na2S), and Nokes reagent (P2S5+NaOH)). However, these depressants are usually toxic or hazardous. Therefore, various methods have been developed to replace these toxic and hazardous depressants, for example, by synthesizing new non-toxic or low-toxic depressants or by using various oxidation methods such as sodium hypochlorite in an alkaline medium, manganese dioxide, oxygen, ozone, and plasma pre-treatment (Arbiter and Young 1951; Barzyk et al. 1981; Curtis 1941; Hirajima et al. 2014, 2017). Recent study by Chimonyo et al. (2016) reported the effect of H2O2 on reducing the recoveries of sulfide minerals. Moreover, Hirajima et al. (2017) demonstrated that H2O2 depressed the floatability of chalcopyrite and could deliver a selective separation on copper and molybdenum (Cu-Mo) bulk concentrate in flotation process. However, they reported that this method required a higher concentration of H2O2 and a longer treatment time (4.5 h) to get a comparable result to that of using NaHS as copper depressant. Therefore, further improvements are necessary to reduce the conditioning time and reagent consumption."

Jan 1, 2018

By C. Hazotte, M. -O. Simonnot, V. Houzelot, B. Laubie, M. Guilpain, B. Jally

"More than 400 plants in the world are able to accumulate nickel (Ni) in their aerial parts at concentrations higher than 10 g per kg of dry biomass. Then, Ni can be recovered from the biomass of these hyperaccumulator plants. Agromining is a chain consisting in growing such plants and producing metal. It has been developed thanks to the combined know-how of agronomy and hydrometallurgy. Hydrometallurgical processes have been designed; two different pathways were developed: i) acid leaching of ashes after biomass combustion and ii) direct Ni water extraction after biomass grinding. Experiments with 2 species of Ni hyperaccumulators (A. murale from the Balkans and R. bengalensis from Malaysia) have shown that the first process is very robust and transposable. For the second one, the way Ni is stored in the plant has a strong influence on extraction. A. murale transformation was explored in more details from the lab scale to the pilot scale. Results proved that Ni is totally transferred into the aqueous phase after 2 hours at 90 °C. A life cycle assessment has clearly shown the environmental interest of this approach (especially by detoxifying agricultural soils). INTRODUCTION Agromining is an emerging phytotechnology aiming at recovering metals thanks to hyperaccumulating plants (van der Ent et al., 2018). These plants are able to accumulate very high concentrations of metal in their aerial parts. For example, for nickel, the hyperaccumulation threshold is 0.1%, i.e. 10 grams of metal per kilogram of dry biomass. There are some advantages to use this technology instead of conventional mining techniques: •,Treating unconventional metal resources: they can be (i) natural soils with low concentrations but also low fertility because of the metal presence (like serpentine soils for Ni) (Bani et al., 2015), (ii) mine tailings or (iii) industrial wastes (like surface treatment sludge) after soil construction (Rue, 2017);"

Jan 1, 2018

By J. K. Afidenyo

Microbial pretreatment of a double refractory gold ore was investigated using a white rot fungus, Coriolus versicolor (ATTC 20869) to improve gold extraction. A series of preliminary tests were conducted to determine the amenability of the ore to fungus degradation. Pulp density, temperature, pH and retention times were the process variables considered. Both a single. Stage and two-step processes were studied to establish process conditions. During the single stage process, the ore was contacted with the fungus culture (biotic) for 3weeks at 30°C and pH 10.0. For the two-step process, the first step involves ore contact with the culture medium (abiotic) at 45°C and pH 10.0 followed by fungal contact (biotic) at 30°C. Results indicated that carbonaceous matter is not degraded but passivated by the fungus; as preg-robbing activities dropped significantly from 18.1% to below 1.0%. The single stage process resulted in higher gold recovery than the two-step process Gold ex-traction by cyanidation of the pretreated ore was 78.9% for the single stage compared with 15.0% for the untreated ore. In the two-step process, only 73.3% gold extraction was achieved. Application of the two step process conditions to a high grade flotation concentrate, resulted in 93.3% gold ex-traction as against untreated concentrate of 30.5%. The results show that the microbial pretreatment process degraded sulfide sulfur, passivated carbonaceous matter and enhanced gold extraction from double refractory gold ore and concentrate.

Jan 1, 2014

The quality of iron ore fines in terms of high iron content and low levels of deleterious impurities such as Silica, Alumina, Sulphur and Phosphorous is a critical parameter, in sintering and subsequent iron and steel making processes. As the higher-grade ores become depleted, there will be a stronger focus on treating lower-grade haematite/goethite ores and developing suitable beneficiation techniques to reduce the levels of impurities. Innovative flow sheets, based on new and commercially available technologies, is required. These will be needed to include gravity concentration devices, which can handle coarse and fine feed sizes. In this paper, efforts made to reduce the silica and alumina content of a low grade iron ore fines (<1.0 mm size) sample from the Pilbara region in Western Australia are described. The feed sample, a goethite abundant lower grade iron ore fines, which was a plant reject assaying 48.66% Fe with 13.61% SiO2and 5.09% Al2O3 was investigated. To this end, an experimental campaign was undertaken, and beneficiation studies were conducted on the sample using a Floatex Density Separator (FDS), a gravity device which can be operated for size classification and/or relative density separation. The objective was to produce high-quality iron ore material suitable as sinter feed. An iron concentrate with a grade around 57.0% Fe (Calcined Fe of about 63.0%) was achieved while recovering around 67.0% of the feed weight. In addition, a rejection of substantial content of Silica (>75%) and Alumina (>66%) was achieved while securing >77% iron recovery. On the other hand, sharp classification efficiency with low values of imperfection around 0.20 was obtained. Consequently, the response of the lower grade iron ore sample to FDS application, has vast potential to reject deleterious impurities as a single stage separating beneficiation equipment. Remarkably, it was demonstrated, that a great amount of goethite, abundant in lower grade iron ore fines/plant rejects, which are currently being either stockpiled and/or dumped as waste, can be treated using FDS application and potentially can add a significant value to the iron ore mining industry by recovering additional iron ore fines. Keywords: deleterious impurities, beneficiation techniques, classification, relative density separation

Sep 1, 2012

By J. C. Wilmot

The chemistry of aqueous cyanide containing species in the presence of reduced sulfur sources was investigated. Reactions were studied as a function of time and tracked using novel analytical techniques developed for the analysis of the species of interest in the sample matrix. Species of interest in this work were ?free? cyanide, thiocyanate, cyanate, metallo-complexed cyanide, and various sulfur and sulfur-oxygen species. The studies were conducted under constant temperature conditions at pH values above 10.5 and in the absence of light in order to eliminate photochemically induced cyanide reaction effects. The reaction products of cyanide when in contact with pure sulfur, pyrite, pyrrhotite, sphalerite, and cinnabar are reported. These data combined with data for cop-per, arsenic and lead sulfides, which have been previously published, are used to predict the fate of cyanides in refractory gold ores containing sulfides. A mass balance on the cyanide reaction products was completed for all experiments. From these studies insight into the chemical relationships of cyanide, the specific metal sulfide, thiocyanate and cyanate have been gained. When looking at the results of the experiments, it was immediately apparent that even though the overall conversions of cyanide to thiocyanate were different, most of the samples exhibited a similar pattern of reactions. The recovery of cyanide in these experiments was better than we expected, averaging in most experiments to be over 90 percent. Based on this research, the formation of cyanate was probably the main route of loss. The pathway choice for the various minerals was also elucidated in these experiments. The competitive oxidation pathways that cyanide can take have been tracked for sufficient time to determine the ?final? fate of cyanide in a process. Initially, it was thought that the cyanate may be involved in a hydrolysis reaction to form ammo-nia and carbonate ion, but upon further inspection of the data, there was not the drop-off in total cyanide recovery that would manifest itself were this to happen. On the other hand, the hydrolysis of thiocyanate to cyanate and sulfate would require oxidizing conditions which did not exist in solution at the beginning of the experiment. If the solutions were to be sufficiently oxidizing in nature for this to happen, the initial amount of cyanide would have been converted to cyanate quickly. The data support premise that the ?hydrolysis? of thiocyanate to cyanate and sulfate occurs to some extent in the experiments conducted. Knowledge gained from the experiments with pure metal sulfides helped interpret the results of experiments with refractory ores found in the State of Nevada.

Jan 1, 2014

By G. Bulut, Ü. Yenial

"Heavy metals contamination in aqueous systems can be found in a variety of industries, in particularly mining, metal processing, finishing and plating. Water containing more than 0.5 ppm heavy metal considered as a toxic due to harmful effects on health. The major techniques employed for heavy metal removal from industrial wastewaters include precipitation, reduction, ion-exchange, and adsorption. Adsorption is a heavy metal removal method for aqueous systems. As a common adsorbent, activated carbon has been used in treatment but it is ineffective on some elements. Thus, there has been a research for developing highly effective and selective adsorbents. In this study the adsorption of lead and arsenic ions on to coal waste and red mud waste was studied. The experimental parameters were determined as pH, equilibrium time and the initial concentrations, activation by heat treatment and the blend of adsorbents. According to their adsorption capabilities, red mud was found to adsorb lead and arsenic ion with high efficiency but coal waste did not adsorb arsenic ion. However the binary adsorptions of these ions were enhanced the adsorption efficiencies. In addition the blend of coal waste and red mud affected the adsorption efficiency. INTRODUCTION As a result of rapidly developing industry and excessive use of water resources, the need of clean water and wastewater management appear as a problem. Wastewater recycling activities and researches come to the fore for an effective use of wastewater. Recycling of wastewater, which contains heavy metals harmful to the environment and human, is a difficult process. Heavy metals are generally divided into three categories: toxic metals, precious metals, radionuclides. Wastewaters from various industries, containing heavy metals, are the main polluters of water and soil. Although their toxic structures, heavy metals are used extensively in industry as they have technological significance. Usually mining industry, metal industry and industrial organizations produce heavy metal containing wastewaters (Volesky 1990, Ting and Lawson 1991, Bishop 2002)."

Jan 1, 2018

By T. Surkova

For the moment reserves of high-grade ores are practically depleted requiring ever-increased involvement of low assay raw materials, such as black-shale ores, in industrial operations. Black-shale ores are constituted of minerals containing such valuable components as vanadium, uranium, molybdenum, manganese, and rare-earth elements (REE). We studied technogenic solutions of black-shale ores processing, after uranium, molybdenum, and vanadium were recovered. Mentioned solutions contain rare-earth elements in substantial quantities (S REE 70-100 mg/dm3) that is very important factor taking into consideration the world demand ever-increasing last years. Higher concentrations of iron and aluminum inhibiting REE sorption and extraction recovery are found in solutions. We propose a method of hydrolytic deposition to cleaning solutions from impurity elements (Fe, Al). Study of hydrolytic deposition kinetics allowed identifying optimal conditions to run this process. Rare-earth elements may be recovered from purified solutions through sorption process followed by their further deposition from eluates in form of concentrates. Keywords: black-shale ores, rare-earth elements, a method of hydrolytic deposition, impurity elements, sorption

Sep 1, 2012

By G. Sedelnikova

This paper is aimed to elucidate the problem of copper losses in pyrometallurgical slag. Currently, flotation is used to recover copper from the slag and return the metal into the pyrometallurgical process, but the percentage of recovery frequently remains unacceptable. The process of copper leaching from the slag flotation tailings using biologically regenerated ferric sulfate is considered here as an approach to the issue. A sample of the slag flotation tailings containing 0.67% Cu and 4.99% Zn was supplied by the Urals Mining and Metallurgical Company (UGMK, Russia). The Cu and Zn speciation analysis of the sample demonstrated that Cu occurred as 58.1% oxide, 15.4% native Cu, and 18.1% secondary sulfides whereas chalcopyrite proportion was as low as 8.4%. Prevailing Zn species were refractory (58.9% Zn ferrite), and zinc oxide and silicate species made just 37.2% of the total metal content. The silicate generated silica gel that strongly hampered filtration. As demonstrated, Cu recovery is a possibility, which is apparently not the case with Zn. In this work, the stirred tank bioreactor acid leaching employing bacterial Fe3+ sulfate solutions was studied, with ferric sulfate being a product of Fe2+ biological oxidation and not the chemical reactant adding of Fe3+ sulfate. Acidithiobacillus, Sulfobacillus, and Leptospirillum bacilli were employed in Fe2+ biooxidation. Temperature, pH, Eh, S:L ratio, leaching time, and Fe3+ concentration in the source leachate as the process controls were considered. As demonstrated, the process employing biologically regenerated ferric sulfate proved to be more efficient than conventional chemical leaching. Under the optimum conditions, the proportion of Cu extracted into leachate during 2 hours was 79.1%, and that of Zn 27.2%. Precipitation of high-grade Cu sulfide served to extract the metals from the leachate, and Cu extraction was 99.7%. All in all, 23.2% Cu, 0.03% Zn, and 0.02% Fe was returned into the pyrometallurgical process. Keywords: slag flotation tailings, copper leaching

Sep 1, 2012

By S. L. Gao

Based on the differences in hardness and density of diaspore and aluminosilicate minerals which usually exist in Chinese diasporic bauxite, It is analysed that bauxite of this kind is difficult to be separated effectively by classification and normal gravity separation, and cyclonic centrifugal field was thus proposed to be carried out, in which classification can take place according to the size difference resulted from selective grinding, what?s more, the separation function according to density difference is expected to take effect at the same time, and then cyclonic separation tests for diasporic bauxite of A/S 4.39 and grinding 61.90% -0.074mm were carried out tentatively. The results showed that the accretion of feed pressure can offer strong enough centrifugal force for cyclonic separation with result that separation function according to density difference is effectively intensified, by the increasing of this parameter, underflow and overflow of A/S 7.64 and 2.18 can be processed at the same time, and the recovery of Al2O3 in underflow is 71.78%; judging by the flow ratio, the spatial locality envelope of zero vertical velocity do constringe to the vertical axis by the enlarging of diameter ratio of apex to vortex, overflow and underflow of A/S 2.08 and 6.5~7.0 can be processed by controlling this structural parameter, which is possible to offer a technological method for low-grade bauxite to de-sliming beforehand.

Jan 1, 2014

By Qingming Feng, Dongbo An, Jinhong Zhang

The application of the geopolymerization of mine tailings as construction materials is hindered by the fact that conventional geopolymerization of mine tailings usually involves a large consumption of alkali, i.e., sodium hydroxide (NaOH), and a long curing time, because of the relatively low reactivity and the high Si/Al ratio of mine tailings when compared to other active resources such as fly ash and clay minerals. The present study is focused on efficiently activating mine tailings, reducing alkali consumption, decreasing curing time and improving compressive strength. We firstly investigate the temperature effect on the alkali activation of mine tailings during geopolymerization. Secondly, the impact of additives, i.e., calcium hydroxide and aluminium oxide, on the compressive strength of samples is studied. Thirdly, different forming pressures have been applied to remove excessive alkali and its impact on samples&apos; strength has been investigated. The results show that a 40 MPa unconfined compressive strength (UCS) can be achieved with the geopolymerization samples after mine tailings are activated by sodium hydroxide at 170°C for 1 hour with the addition of calcium hydroxide and alkali dissolved aluminium oxide, further compressed with a 10 MPa forming pressure and finally cured at 90°C for 3 days. The findings of the present work provide a novel method for the geopolymerization of mine tailings as construction materials.

Jan 1, 2014

By I. Y. Titov, Victor D. Samyguin, A. Y. Nikitin

"It is suggested that improvement of separation process efficiency in machines and circuits of selective flotation should be based on application of the principle of technology individualization (PIT). This principle is grounded on the following provisions.The mineral composition of ores is used to establish the correlation between the selective reagent mode and the individual value of hydrodynamic conditions of flotation machines together with individual structure of the process flow diagram. The individuality of all sorts of particles identified by methods of process mineralogy was characterized by their distribution according to the rate of flotation (or spectrum). The spectrum identification is carried out by modeling and by experimental and computational method on the data obtained on various types of laboratory flotation machines.The computer-aided test is used to determine the optimal fraction distribution, which reaches the highest possible level of concentration data. The direction of hydrodynamic factors action on concentration data is estimated based on comparison of design base and experimental spectrum. The improvement of separation efficiency in devices is achieved in special-purpose flotation machines (SFM) the design of which provides optimization of hydrodynamic regime in spatially isolated zones. It is demonstrated that the main parameter of SFM operating mode individualization is the rise rate of bubbles going from the chamber into the froth. During this time the composition of particles optimum for separation is formed on its surface. Additionally, it is necessary to coordinate in the zones the residence time of pulp and foam streams with the air consumption. The improvement of separation efficiency in flotation process flow diagrams may be achieved by making several cascades with SFM installed in them. The individual effective structure of the scheme for a definite ores material composition depends on the ratio of particle varieties in the spectrum and is revealed by modeling."

Jan 1, 2018

By A. E. Sobolev

The kinetics of hydrochemical oxidation of antimonite in solutions of nitric acid was studied using the rotating disk method and the factor experiment design. The dependences of the antimonite?s oxidation rate on concentration of nitric acid solutions, temperature, disk rotation frequency, and duration of interaction were determined. The adequate kinetic models allowing calculating the specific oxidation rate at any combination of the values of the influencing factors were obtained. The oxidation process is found to proceed in a mixed mode, close to chemically controlled. Gradually, as the sediments of elemental sulphur and Sb2O5 accumulate on the disk surface, the process becomes controlled by internal diffusion. The observed high (more than second) order of the oxidation rate with respect to the concentration of nitric acid was explained by the autocatalytic action of the acid reduction products. The apparent activation energy depends on the stage of interaction. At the initial stage (in a mixed mode of the process proceeding), it depends on nitric acid concentration and varies from 31.5 kJ?mol?1 (in 2 M HNO3) to 36.1 kJ?mol?1 (in 10 M HNO3). This trend indicates the weakening of diffusion limitations with a nitric acid concentration increase. When the process is controlled by internal diffusion, the apparent activation energy was found to be 14.5 kJ?mol?1. The obtained kinetic characteristics enlarge the database on hydrochemical oxidation kinetics of sulphides and can be used for the elaboration of the recommendations for the effective comprehensive exploitation of antimony-bearing ores and concentrates.

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 H. Y. Ran

Magneto-flotation is a recently developing technology of mineral processing. This technology combines the traditional magnetic separation with flotation and provides a magnetic and buoyant force compound field to separate different minerals based on the differences of magnetism and floatability between useful minerals and gangue minerals. Magneto-flotation is applicable to separate ferromagnetic from nonmagnetic minerals, especially to separate magnetite from floatable gangue minerals. This magneto-flotation column is equipped with pulse electromagnetic field in the middle upper part, a bubble producer and upwell water inlet in the bottom. The pulse time of electromagnetic field in the column can be optionally adjusted and the maximum intensity of pulse magnetic field can reach 35mT. Pulse magnetic field can not only restrain magnetic minerals from entering into the froth layer, but also destroy the magnetic agglomeration to ensure a higher recovery and a higher concentrate grade. The results of experiments with magnetite show that pulse magnetic field has remarkable influence on flotation process. Compared with single flotation, magneto-flotation column can improve the recovery of magnetite by ten percent. After one time?s magneto-flotation processing, the grade of iron concentrate can increase from 65.4% to 69.5%, the content of silicon oxide in iron concentrate decreases from 7.4% to 2.8%, and the total recovery is above 96%.

Jan 1, 2014

By Y. Foucaud, I. Filippova, L. Filippov

Flotation is the most common beneficiation route for tungsten ores, but the predominance of minerals with similar surface properties poses a real challenge. This study investigates the use of Falcon centrifugal separators for gangue minerals removal and desliming prior to flotation. A typical tungsten-bearing skarn ore (Tabuaço, Portugal) is used, containing scheelite (CaWO4) associated with dense calcium-bearing silicates (vesuvianite), fluorite, apatite and light silicates (feldspars) as gangue minerals. Two types of Falcon bowls (Falcon UF and Falcon SB) were used, prior to flotation tests with fatty acids as collectors and a combination of sodium carbonate and sodium silicate as gangue minerals depressants. This flowsheet was compared with a reverse configuration, using flotation prior to Falcon concentrator, and with a classical flowsheet, using hydrocyclone and flotation. Gravity pre-concentration and desliming with the Falcon concentrator were optimized through the design of experiments (DoE) methodology. The influences of pulp density, rotational speed, feed flowrate and fluidisation pressure (for the Falcon SB) were studied for both bowls. Results showed that the Falcon can be used as a desliming and pre-concentrating apparatus. Separation performances depend mainly on rotary speed and pulp density for the Falcon UF, whereas rotary speed and fluidisation pressure are the main parameters for the Falcon SB. With only one stage of Falcon SB, an enrichment ratio of 7.9 is obtained with a 65% WO3 recovery while 89% of apatite and fluorite are rejected, which constitutes a very good selectivity. In comparison, Falcon UF shows lower enrichment ratios, around 2.7. In terms of desliming, Falcon UF is as efficient as the hydrocyclone, while the Falcon SB is significantly more efficient. Hence, the use of Falcon SB prior to flotation improves the overall performance of the tungsten flotation route by desliming the flotation feed while pre-concentrating the scheelite. It impacts very advantageously the flotation, as most of the calcium-bearing minerals are eliminated. A Falcon SB stage prior to flotation yields a final concentrate grade of 29.7% WO3 with a recovery of only 36.8 % that should be optimized as the reagents dosages were not adapted to the pre-concentrated feed.

Jan 1, 2018

By Andrey V. Yevdokimov

The results of the test work on gold leaching using high strength of cyanide solution in the presence of activators are presented. The major physical and chemical relationships of gold leaching were determined. Intensive cyanidation results of gravity concentrates with various material compositions using an activator are given. Process design criteria for intensive cyanidation unit were developed on the base of pilot plant test results. Keywords: gold, activators, intensive cyanidation, gravity concentrates

Sep 1, 2012

By A. Usov

The studies carried out by the Russian researchers and those carried out jointly within some contracts with scientific organizations and companies of other countries, show that the electric pulse disintegration of materials (ED), proposed and investigated in detail in Russia (Kalyatsky, et al, 1980; Usov et al, 1987; Semkin et al, 1995; Usov and Tsukerman, 2000; Kurets et al, 2002) has been widely recognized and developed abroad (Andres, 1995; Inoue et al, 2000; Biela et al, 2008). The Russian and international journals and the proceedings of the conferences dealing with the electric pulse disintegration pay great attention to the principal principals of selective disintegration of materials. There is no, however, any information concerning both the technical means developed to implement the technique and the assessment of their performance, which would be necessary in objective assessment of the industrial use of the technology. The results of long-term studies of the technique and technologies of electric pulse disaggregation by research institutes such as Research Institute of High Voltages (Tomsk), Kola Science Centre of RAS (Apatity), Institute "Mekhanobr"(S.Pertersburg) described. Exploratory stands and technological installations are developed to carry out pilot tests and operations under production conditions. Basic circuits and classification of technical means electric pulse disintegration of the materials are proposed, the analysis of transportation schemes and classification of the material in the disintegration apparatus are given, construction of chambers for continuous stadial disintegration of ores and materials are presented. The features and technological efficiency of electric pulse disintegration of various types of ores, and the spheres of effective use of the method have been determined. Keywords: electropulse disintegration, disintegration machines, chambers of comminution, stadial comminution.

Sep 1, 2012