Search Documents

By D. J. Borrow, K. van Netten

"A fine coal tailings feed was selectively agglomerated using a concentrated water in oil emulsion binder consisting of 95% aqueous phase and 5% organic phase. The purpose of the study was to investigate a continuous system in plug flow, providing a rapid beneficiation technique with high selectivity and recovery. The development of the novel binder was undertaken in previous work in a batch system consisting of a high-speed blender. In this previous work, it was found that agglomeration could be achieved in 3 s, providing the binder was pre-dispersed. Furthermore, it was found that, depending on the feed, only ~1 wt% of oil was required to achieve agglomeration, some 10 times less than required in traditional oil agglomeration. In a more recent study, the technique was adapted into a continuous process. Due to the rapid speed of the process using the emulsion binder it was found that a simple flow constriction within a 1 inch pipe was sufficient to achieve the selective agglomeration observed in the batch system. In this previous study, a coal feed consisting of a flotation product was agglomerated at a superficial slurry velocity of 1.3 m/s using a partially closed ball valve as the flow constriction. In the current study, a feed consisting of fine coal tailings with an ash content of 50.1% was used to establish the influence of superficial slurry velocity on the agglomeration process. The superficial slurry velocity was varied between 1.3- 4.2 m/s, while maintaining a constant pressure drop of 100 kPa across the flow constriction. The flow constriction consisted of a partially closed ball valve. It was found that increasing the superficial slurry velocity across the flow constriction reduced the amount of organic liquid required to achieve agglomeration. Under the optimum conditions, a combustible recovery of 80.4% was achieved at a product ash content of 9.6%. This work demonstrates a valuable product can be rapidly produced from tailings material using the novel emulsion binder. INTRODUCTION A significant opportunity exists to recover fine coal from material that is currently classified as waste. This waste material, also called tailings, is currently considered not economic to process due to its high ash content, low solids concentration, and the fine size of the particles. Thus, for this opportunity to be realised, a process is required that is highly selective and has the ability to economically recover fine particles at high throughputs. The technique of oil agglomeration has previously been considered as a candidate for the recovery of fine coal, as it is highly selective and has no lower limit on the size of particle that can be recovered (Capes and Jonasson, 1989). However, the cost of the oil required as the binding agent in the process has proven to be a significant barrier to any long-term applications (Swanson, Nicol, and Bensley, 1977). Recently, however, Yoon and co-workers have developed an ultrafine coal separation process that utilizes an oil phase for the recovery of the hydrophobic coal particles and have implemented an oil recycle to greatly reduce the consumption and thus cost of the oil (Yoon et al., 2016)."

Jan 1, 2018

By H. D. Mendoza, M. J. C. Zerna

This study aims to determine the stability of Philippine nickel laterite ore by investigating the behavior of fine minerals of silica (dave=1.514 µm), hematite (dave= 0 1.351 µm), and nickel oxide (dave=1.426 µm) and their mixed-components in dilute aqueous suspension as a function of pH and electrolyte concentration. The zeta- potentials of the minerals are measured and stabilities of different component systems in aqueous suspension are determined. Hamaker constants of the minerals in aqueous medium are derived by getting their respective critical coagulation concentrations (c.c.c.) at stable pH conditions and at various concentrations of KNO3. The iso-electric points (i.e.p) for silica, hematite, and nickel oxide particles are at pH 2, pH 7.5, and pH 8.5, respectively. The stability behaviors of component systems are as follows: a) Silica dispersion is stable at pH range 3-11and unstable at pH 2; b) Hematite dispersion is stable at pH 2-5 and pH 8-11, and unstable near pH 7; c) Nickel oxide dispersion is stable at pH range 10-11 and unstable at pH 3-9; d) Hematite-silica dispersion is stable at pH range 6-11 and unstable at pH range 3-5; e) Hematite-nickel oxide dispersion is slightly stable at pH range 3-4 and unstable at pH range 5-11; f) Silica-nickel oxide dispersion is stable at pH range 10-11 and unstable at pH range 3-9; and, g) Hematite-silica-nickel oxide dispersion is stable at pH range 10-11 and unstable at pH range 3-9. The stability of nickel laterite ore is similar to that of the three-component system in an aqueous environment. The stability tests are analyzed using the classical DLVO theory. The stability conditions in an aqueous environment are essential in developing the appropriate process flow for the separation/ recovery of nickel laterite mineral components and also in the treatment of nickel laterite -laden wastewaters.

Jan 1, 2018

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

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

Jan 1, 2014

By Hongchun Lou, Yan Zhang, Xianjun Lu

"The potential of Fe(NO3)3 modified attapulgite was assessed for the adsorption of phosphorous removal from aqueous solutions. Natural attapulgite was modified by Fe(NO3)3, and thus the composite adsorption materials could be obtained. Also phosphorous adsorption characterization on the iron-coated attapulgite was investigated in this research. Taken overall the results suggested that phosphorous adsorption capacity could be improved markedly by adopting ferric modified-attapulgite. The optimum phosphorous adsorption were developed in the experimental conditions of the solid-to-liquid Ratio 1g/L, the initial phosphorous concentration 5 mol•L-1, reaction time 120 min, temperature 25 ? and pH=4.0, the removal efficiency is 92.28% for the modified attapulgite. In comparison of batch experimental results of phosphorous adsorption onto natural and iron-coated attapulgite, it has provided much more likely the same change trend. On the other hand, the outcomes of this analysis indicated that ferric modified adsorbent was notably influenced by adsorption element over natural attapulgite. The Freundlich isotherm adequately described the adsorption course of phosphorous onto ferric modified-attapulgite with the correlation coefficient R2 goodness of fit of 0.9690."

Jan 1, 2014

By l. Bokányi, T. Varga

"The recycling of waste car tyres is a very important environmental task. The waste tyres usually are re-used or recycled by thermal processes like pyrolysis, gasification or incineration. The main problem associated with these processes is the sulphur content of waste tyres originated from the vulcanisation process, which pollutes the environment and the valuable products (i.e. pyrolysis oil) as well. In our research the desulphurisation of waste, mechanically prepared tyre sample was systematically investigated by the biosolubilisation with Acidithiobacillus thiooxidans, strain Karitas. Parallel, the experiments with sterile 9K nutrient medium were also carried out. It was found that the vulcanisation sulphur can be solubilised due to both the bio- and the chemical leaching, although the bioleaching is more effective. The solubilised vulcanisation sulphur then forms precipitates. The precipitates are forming in the bulk solution, as well as on the surface of rubber particles. The origin of the precipitates was investigated using XRD and scanning microscopy with micro probe. The origin of the precipitates is different: while in the process of the vulcanisation sulphur solubilisation with 9K medium the jarosite (KFe3+3(SO4)2(OH)6) forms, the course of the biosolubilisation with Acidithiobacillus ferrooxidans Karitas is accompanied by the formation of the jarosite and the halotrichite (FeAl2(SO4)4 · 22H2O) as well. The formation of the latter is the biomineralisation. The mechanisms of the bio- and chemical solubilisations are rather different as it was found and experimentally proved by several tests, and depends on the retention time of the solubilisation. Special efforts were done to elaborate the proper separation of the precipitates from rubber particles. Combination of intense dynamic stirring and recycling flotation process to remove the precipitates was applied for this purpose. The surface properties of synthetic jarosite were revealed using zeta-potential measurements at different pH and in presence of collectors. The parameters of the flotation were chosen based on the revealed surface properties of the precipitates. Finally, the sulphur recovery of the recycled rubber was achieved as low as <0.5%, sulphur content of it 0.17%, 12-times lower than that of the waste tyre sample after mechanical preparation."

Jan 1, 2018

By Tamara F. Kondrateva, Evgenia E. Savari, Galina V. Sedelnikova, Rauf Y. Aslanukov, RAS (INMI), Grigori I. Karavaiko

"The investigation is dedicated to study of biohydrometallurgical processing of refractory gold-arsenic concentrate with the large content of pyrrhotite. Sulfide concentrate of chemical constituents: 75g/t Au, 4,7g/t Ag, 6,3% As, 29,3% S, 2,3% Sb, 0,5% ? (organic) and of mineral composition, %: 11,8 arsenopyrite, 39 pyrrhotite, 12 pyrite, 2,9 antimonite and the rest – aluminosilicates, carbonates and quartz, was studied. The recovery of gold from concentrate by cyanidation is 51,2%. The rest of gold is embedded as finegraded segregation in sulfides.Sulfide oxidation process study is described. Bacterial oxidation was executed on a pilot laboratory unit using combined autotrophic bacterium: A. thiooxidans , A. ferrooxidans, Leptospirillum ferrooxidans and sulfobacillus thermosulfidooxidation, pH=1,5-2,2, t=28-32?C, oxidation time 120 hours. Pyrrhotite is the least stable sulfide mineral with electrode potential 0,45V versus arsenopyrite (0,55 V) and pyrite (0,55-0,6 V) and is oxidated primarily. Pyrrhotite oxidation is followed by large amount of elemental sulphur, which has a bad influence on cyanidation.It’s established that the rate of arsenopyrite (for the first 48 hours) from concentrate containing 39% pyrrhotite is 2-3 times as less as the rate of arsenopyrite bio-oxidation from concentrate without pyrrhotite. The arsenopyrite bio-oxidation is accelerated only after the elemental sulfur was oxidized by bacterium A. thiooxidans and elemental sulfur percentage was reduced from 6,8 to 3,9%. The bacterium concentration is increased from 2,5x107 to 2,5x109 cells/ml. Almost full oxidation of arsenopyrite (98%) and pyrrhotite (98- 99%) is finished in 120 hours. We have studied two pretreatment methods for elimination sulfur content influence on cyanidation: aeration in lime and electrochemical treatment. Such an operation enables to have supplemental oxidation of elemental sulfur and other oxygen and cyanide absorbants before cyanidation. After treatment the content of elemental sulfur was decreased from 3,9 to 2,2%, gold recovery from 90 to 96% and cyanide consumption from 16,2 to 7,2 kg/t decreases. The content of toxical rhodonite-ions in liquid phase of pulp and disinfection reagents consumption were decreased as result of elemental sulfur content in bio-oxidated product reduction."

Jan 1, 2003

By Xie Jiyuan, Hu Yuehua, Yang Songrong, Zhu Zhansheng, Qiu Guanzhou

"By the end of 2000, the first bio-oxidation plant in China that designed by ENFI come successfully into commercial operation in Yantai Gold Smeltery. Its capacity is 50t/d of refractory gold ore concentrate. After the extension, the capacity of bio-oxidation plant reached 80t/d of refractory gold ore concentrate at end of 2001.The refractory gold ore concentrate treated is from different gold mines. After proportionate feeding, the feed typically consists of Au (52.7g/t), S (24.42%), As (3.58%).The bacterial culture used in the bio-oxidation circuit is taken from a mine in south of China, and has been grown over 20 years on a variety of sulfide concentrates in a laboratory of mineral processing, and has shown to be adaptive to growth in a high concentrations of arsenic. It is a mixture of mesophilic microorganisms. The nutrients used in the bio-oxidation process are (NH4)2SO4, KH2PO4, KOH.Before feeding to bio-oxidation circuit, the concentrate would be milled to minus 43µm. The biooxidation product is fed to solid/liquid separation system that consists of a thickener and two press filters, solid from the system is fed to CCD circuit, liquid from the system is fed to neutralization area. The neutralized product is fed to another solid/liquid separation system, and the solid from the system is disposed of on a wasted quarry pit, the liquid from the system is returned to bio-oxidation circuit for reusing."

Jan 1, 2003

By P. Altinkaya, O. Celep, H. Deveci, E. Y. Yazici

"Copper-bearing gold ores have proved difficult to treat in conventional cyanide leaching process owing to prohibitively high consumption of cyanide by readily soluble copper minerals interfering with gold extraction. Cyanide leaching of gold from copper-rich ores can be improved by intensive cyanidation or application of physical and chemical pre-treatment methods (e.g., ultra-fine grinding, roasting and leaching). In this study, nitric acid leaching of a copper-bearing pyritic concentrate (0.3% Cu, 62 g/t Au and 110 g/t Ag) as pre-treatment prior to cyanidation was investigated. The mineralogical analysis of the concentrate has revealed that it is composed of mainly quartz (25%), pyrite (32.7%), sphalerite (5.37 %), galena (2.12 wt %) and anglesite (1.13 %). Arsenopyrite, chalcopyrite, covellite and bournonite were also detected as minor phases present. Previous studies carried out by the authors showed that direct cyanidation (1.5 g/L NaCN) of the as-received concentrate (d80: 80 µm) produced low gold (45% Au) and silver (46% Ag) extractions. Nitric acid pretreatment of the as-received concentrate was performed for 5 hours at 1-5 M HNO3 and 80oC. In these tests, 65% Cu/Pb and 94% Zn were leached. The nitric acid pre-treatment improved the extraction of gold and silver in subsequent cyanide leaching (1.5 g/L NaCN) to 82% Au and 87.5% Ag with a concomitant decrease (up to 54%) in cyanide consumption. It can be inferred from these findings that the removal of copper from the concentrate and the liberation of the occluded gold by nitric acid leaching as pretreatments can be appropriately employed for the treatment of the copper-bearing pyritic concentrate with high gold/silver content. INTRODUCTION Refractory ores are often characterized by their low amenability to cyanide leaching resulting low (often <80%) Au/Ag extractions (Bhappu, 1990; Celep et al., 2009; Marsden and House, 2006). One of the most common causes of refractoriness is the physical or chemical encapsulation of submicroscopic or fine-grained gold in sulphide minerals such as arsenopyrite and pyrite (La Brooy et al., 1994; Vaughan, 2004). To render refractory gold ores/concentrates amenable to cyanide leaching, the decomposition of sulphide minerals within a pre-treatment process to expose the encapsulated gold grains to the action of cyanide is required. In this regard, roasting, pressure oxidation and biooxidation are commercially used processes for pretreatment of arsenopyrite/pyrite gold ores/concentrates ahead of cyanide leaching (La Brooy et al., 1994). Presence of cyanide-soluble copper minerals in the ore leads to low gold recoveries and high cyanide consumptions under conventional cyanide leaching conditions. High cyanide concentrations (CN:Cu>4) should be employed to achieve high gold recoveries from copper-rich gold ores/concentrates. This may require recovery of cyanide from effluents. In this regard, SART Process (sulphidisation-acidification-recycling-thickening) employed industrially for recovery of cyanide and copper as a by-product. This process simply relies on the addition of sulphide (as Na2S, NaSH or H2S) to the leach solution prior to the acidification to pH 4-5. This results in the precipitation of copper as Cu2S and occurrence of free cyanide which is recycled to the leaching circuit after S/L separation (Dai et al., 2012)."

Jan 1, 2018

By L. A. Vaisberg

"Crushing and grinding are the two most common industrial processes. These processes consume nearly 20 per cent of the entire electric power produced worldwide. This enormous amount of electric power consumed results from the fact that modern crushing and grinding machines employ the processes first introduced by the prehistoric man, namely those of compression, impact, attrition, and cutting. The material thus handled decomposes indiscriminately, and almost completely ignoring the microscopic cracks and other defects of its structure. Apart from the irrational use of the power, the crushing and grinding processes currently in use result in irretrievable loss of useful components or else in a substantial deterioration of the final products obtained, all as a result of incomplete grinding or, reversely, of overgrinding, palletizing, or fracture of particles.The principal type of equipment that has almost universally been used all over the world for more than 150 years for crushing both natural and synthetic minerals comprises unbalanced jaw and cone crushers. The driving element of crushing bodies in these machines is an unbalanced weight, which transfers the crushing body, allowing it to squeeze the material within the eccentricity value only. The maximum reduction ratio achieved by such a drive is 5, which is due to the rigid kinematic arrangement of the crusher, its dynamic unbalance, and the impossibility of increasing the number of impacts on the material being crushed. Moreover, conventional machines cannot cope with super hard materials, and their mechanism is vulnerable to damage by uncrushable objects.On the basis of fundamental research into the theories of solid body and vibration, OAO Mekhanobr- Tekhnika have developed a range of vibrating jaw and cone inertia crushers that make a reduction ratio of 30 feasible in an open-circuit operation with the reduction ratio monitored within a wide range. In these crushers, the eccentric drive is replaced with a vibrating one. In this way the rigid kinematic drive became dynamic, thus allowing pieces of material to be crushed in a thick layer due to the effect of their bumping into each other, and with the amplitude changing automatically. This results in a number of advantages as compared with conventional crushers:"

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 Matti Kongas, Kari Saloheimo, Antti Remes

"The paper studies the control performance of the flotation process as a function of the measurement accuracy and sampling frequency of an on-stream XRF analyzer, using a simple dynamic model. An additional aim is to assess how the economical result of a mineral flotation process depends on the quality of process control based on the on-line elemental assays.An on-stream XRF analyzer measures the concentrations of slurry lines in a continuous cycle from several process points. The control performance depends on the analytical accuracy and sampling frequency of the concentration measurement. With a long cycle time, the state of the process changes before a new measurement becomes available. With short measurement times the statistical variance of the counted Xray pulses increases, increasing the random error in the analysis. In addition, the measurement accuracy depends on the concentration of the component to be measured from the slurry.To quantify the effect of analysis error and frequency to process control, a simple dynamic process model is created in the Matlab environment. Data from a copper flotation circuit is used as a test case. The process model comprises a first order reaction equation and the grade-recovery -relationship estimated from process data. The control was modeled using the control strategies implemented into a rule based advanced control system. The economical performance of the control was studied by calculating the overall net smelter return at various analyzer parameter combinations."

Jan 1, 2003

By L. Ya Agapova

Emissions from pyrometallurgical processing of copper concentrates are usually subjected to wet scrubbing. The washing sulphuric acid so produced contains up to 0.2 g/L of rhenium, which is recovered by solvent extraction in the form of crude ammonia permeate (NH4ReO4). The mother liquor, obtained from the sulfuric acid wash, contains up to 35 g/L of rhenium and significant amounts of impurities. Crude rhenium salt is commonly processed by double recrystallization to produce marketable salt. A ton of high grade NH4ReO4 can be produced using 3.0-3.5 m3 of mother liquor. We propose an efficient technology of mother liquor pre-treatment aimed at removal of water-soluble organics with subsequent electrodialysis. Electrodialysis of mother liquor in a multichamber electrodialyzer resulted in the production of pure rhenium acid, from which a marketable NH4ReO4 is precipitated using ammonia solution. Multiple steps of recycling consisting of dissolution of NH4ReO4 salt, rhenium acid production from NH4ReO4 salt by electrodialysis and precipitation of NH4ReO4 from rhenium acid made it possible to upgrade the purity of obtained rhenium compounds by 1-2 orders of magnitude. A rhenium metal powder of 99.997% purity was produced by high-temperature reduction of high-purity NH4ReO4 with gaseous hydrogen. Rhenium metal powder of high purity can be produced from sulfate solutions of NH4ReO4 by non-platinum anode-based membrane electrolysis processes also. Keywords: rhenium, mother liquors, membranes, electrodialysis, rhenium acid, ammonia perrhenate, reduction, powder, electrolysis

Sep 1, 2012

By Takashi Furuyama, Sukeyuki Mori, Takafumi Okuma, Norio Hashiguchi

"In order to achieve a high recovery of particles finer than 10µm, three types of dry Tower Mill (VD-1, KD-1, KD-2 and KD-3) have been developed. These mills differ from each other in the size of the comminuting part, the inside diameter and shape of the classifying part and the system involved in the collecting process. The last version (KD-3) of tower mills in which the comminuting and classifying operations has been separated, can produce particles finer than 10µm from a limestone ore sizing from 420 to 3360µm. In this tower mill, products in comminuting section are blown up and transported into the classifying column, made of an inverted cone on top of a cylinder, before they agglomerate and settle down. Fine particles are deported and recovered in a cyclone with a central spiral ribbon.Previous studies on the grinding efficiency of the tower mill KD-3 have shown how the maximum size of collected products increased with the airflow velocity, disturbing in the same way a smooth regulation of the grinding operation with the tower mill KD-3. A complete knowledge of factors that influence the maximum size of collected products is needed, therefore, to increase the efficiency of the grindingclassifying operation and ensure a better control over the collected products. The present study deals with this issue and, assuming that the structure of the classifying column could be one of these factors, its internal structure was modified (insertion of vertical plates, cone or horizontal nets) before carrying out comminution tests that would establish a relationship between the inward shape of the column and the maximum size of collected products. It was found that the weight of products collected in the cyclone decreases when a cone or some horizontal nets are inserted inside the column. At the same time, the weight of products collected in the column increases. This is due to the fact that coarse particles blown up from the comminution section collide with the base of the cone or the nets and settle down the bottom of the classifying column. Therefore, the cone and some horizontal nets inserted inside a classifying column, have the particularity to stabilize the maximum size of particles (15.1-17.5µm and 8.4-11.3µm) in the cyclone even when the airflow velocity in duct increased. These tools could of great help in the production of particles of definite size to fit for instance the paper industries requirements (production of limestone material sizing - 10µm as paper filler)."

Jan 1, 2003

By Y. L. Tian

Low-grade bauxite with A/S of 4.4 from Henan province was used as raw material and the selec-tive grinding of bauxite, grinding efficiency, particle size and Al2O3 and SiO2distributions of ground products were investigated using ball and vibration mills. The results show that the selective grinding can be used to realize the separation of aluminum from silicon within a certain particle size. The optimal grinding conditions of the ball mill with bauxite are as follows: grinding material to charge ratio, 1.2, charge volume ratio, 40%, pulp con-centration, 70wt%, medium size distribution, F30mm:F20mm:F15mm=20%:50%:30%. Under the conditions, the weight rate of ground product with A/S over 7.5 is 27% and the recovery of Al 2O3is 30%. The optimal grinding condition of the vibration mill with bauxite are as follows: grinding material to charge ratio, 0.9; charge volume ratio, 70%; concentration, 70%; medium size distribution, F40mm:F30mm:F20mm=20%:30%:50%. Under the conditions, the weight ratio of ground product with A/S over 7.5 is 25% and the recovery of Al 2O3is 27%. The research is significant for the rational and economical utilization of the low-grade bauxite.

Jan 1, 2014

By Edson Charikinya, Pierre-Henri Koch

"The extraction of mineral values from ore requires liberation followed by separation steps. Liberation is achieved by size reduction operations which are energy inefficient processes typically dominating the energy consumption in a mineral concentrator. As the grade of ore reserves declines, future viability of mineral operations will be determined by energy costs of comminution. The application of high power microwave energy to secondary crusher products has been suggested as a possible commercially viable thermal treatment method for reducing comminution energy and improving value mineral liberation. Recent studies have shown that microwave pre-treatment of coarse sphalerite ore particles (> 5mm) at specific microwave heating energies (1-3 kWh/t), induces microfractures and creates new crack surfaces. This suggests that subsequent crushing of these microwave treated particles could yield enhanced liberation. However, limited studies have been carried out investigating the mode of breakage and the extent of enhanced liberation in that case. The objective of this study is to develop numerical methods for quantifying the extent of enhanced liberation and mode of breakage in crushed microwave treated and untreated particles. Sphalerite ore particles representing small (-5+4.75) mm, medium (-16+9.5) mm, and large (-25+19) mm HPGR and cone crushed particles were microwave treated at specific energies between 1-3 kWh/t. Cracks in the ore particles before and after microwave treatment were analysed with QEMSCAN and numerical models of the measured particles (before and after microwave treatment) were developed in MATLAB. The propagation of random and non-random cracks was investigated by simulating comminution of the modelled treated and untreated particles. Results of this study demonstrate that the breakage mechanism and the liberation of valuable minerals from gangue in microwave treated and untreated particles is significantly different. This study contributes to the development of numerical tools to quantify crack propagation in heterogeneous ore particles."

Jan 1, 2018

By Peter M. Solozhenkin

Considering the main idea of the paper, namely that the interaction energy of reagents serves as a criterion used for their selection, as well as due to their insufficient study, the authors have therefore considered studying the aspects of computer modelling and molecular dynamics of largely used collectors for the flotation of nonferrous and precious metal ores. Three-dimensional molecular models for sulphydric reagents have been created, studying as well the distribution of the partial charges on their atoms. It has been shown that the value of the partial charge on the phosphorus atom in diethyldithiophosphinate and diethylmonothiophosphinate is high positive. The value of the partial charge of the sulphur atom is negative, strengthening its bond with the metal cations from the mineral surface. The molecular orbitals for the sulphydric reagents have been created determining as well the energy of their level. The computer modelling key parameters have therefore been defined. The new reagents have been tested for gold, copper and rhenium ore flotation. Gold recovery has increased with 4.2 - 4.7 %, copper recovery with 3.3 % and rhenium recovery with 15.5 %. A number of new flotation reagents have been recommended, such as: diethyldithiophosphate, (C2H5)2NCH2CH2OC(S)SNa, (C4H9NH)2P (S)SNa and also (C2H5)2P(S)ONa and (C2H5)2 P(O)S Na. Keywords: flotation, molecular modeling, design, orbital?s

Sep 1, 2012

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

By B. Q. Xiao

The nitrate content is an important factor for environmental water samples and flour. In a 0.35 mol/L H2SO4-2NO solution, has a strong catalyzing function on the decolourization of Gallocya-nine (GC) oxidated by NaBrO3. Based on this, a novel method was developed to measure the NO and -3NO concentrations in water and flour. The flow injection technology was introduced into the analysis system. A single-valve dual- cingulums to inject which the Copperized-Cadmium slice and the reduction zone are isolated. The optimum solution for this method contains 1.48×10-4 mol/L GC, 0.06 mol /L NaBrO3 and 0.2 mol /L of NH4-2NOCl. Two empirical equations were proposed to calculate the and -3NO concentrations based on the measured signals. It can be used to measure -2NO of from 0.001 mg / L to 2.0 mg/L and -3NO of from 0.002 mg / L to 2.5 mg/L. The measurement frequency can be up to 20 samples / h. The relative standard deviation for eleven samples is less than 5%.

Jan 1, 2014

By L. Y. Feng

The percentage of leached zinc in massive zinc oxide ores (11.7% Zn, >2 mm) is up to 73.3 % in 120 days. Alternatively, crushed to -0.154 mm, mixed with cement 5% (wt), pelletized and solidified. The diameters of the pellets obtained are between 5 mm to 8 mm. When the pellet solidification periods are 3 days, 10 days and 45 days respectively, the alkaline leaching rates of zinc in the pellets are up to 95.8%, 89.1% and 76.4% respectively. Decreasing the solidification time can re-duce reaction time, increase dissolution of zinc in pellets and lower the effect of initial zinc concentration on leaching rate. The experiment results show that the minimum solidification time is three days, and the kinetic study indicates that alkaline leaching of the low grade zinc oxide pellets is controlled by the diffusion of the leach liquor through the gangue layer in the whole leach process, and the apparent rate constants are 3.33×10-2 day-1, 9.18×10-3 day-1, 5.82×10-3 day-1 respectively.

Jan 1, 2014

By Yu. E. Emelyanov, A. V. Bogorodsky, R. N. Nabiulin, S. V. Balikov

"The paper describes the results of the study of gold-copper flotation concentrate atmospheric oxidation at different sizes of material, varying oxidation time, with air or oxygen blow. The study showed the low rate of sulphide oxidation during oxidation of flotation concentrate at a feed size (P98 -74 µm). The coppery recovery into solution was 48%; the recovery of gold by subsequent cyanidation reached 86%. Preliminary flotation concentrate grinding to P98 -20 µm provided oxidation of 90% of copper minerals, 80% of arsenopyrite and 15% of pyrite. The gold recovery by atmospheric oxidation of a fine-ground flotation concentrate increased by 59%, from 36% to 95%, the NaCN consumption reduced by 21 kg/t, from 30 to 9 kg/t. INTRODUCTION Processing of sulphide gold-copper ores and concentrates using conventional cyanidation technology results in higher reagent consumption and lower gold recovery. Destruction of sulphide minerals and extraction of copper from a processed product prior to cyanidation is essential for improving efficiency of precious metals recovery and reducing main reagents consumption. Atmospheric oxidation (AO) is one of the most promising hydrometallurgical methods of refractory gold-copper concentrates processing, along with biooxidation and pressure oxidation. The nature of this approach lies in oxidation of sulphides at 90-95°C, in acidic or alkaline conditions, with bubbling of oxygen or air, after preliminary ultrafine grinding (1-4). The following reactions of sulphide oxidation occur during atmospheric oxidation of a gold-copper flotation concentrate. Pyrite is oxidized with the formation of ferric sulphate (1) and elemental sulphur at low temperatures (2), whereas some portion of elemental sulphur reacts to form sulphuric acid: FeS2+3,75O2+0,5H2O=0,5Fe2(SO4)3+0,5H2SO4; ?G=-1144,02 kJ/mol (1)"

Jan 1, 2018