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By P. Somasundaran

Treatment of mineral surfaces with appropriate surfactants plays an important role in mineral processing operations such as flotation, flocculation and dewatering. Recently biosurfactants, in particular, have received a considerable amount of attention because of their unique surface active properties and biodegradability. In this work we examined the performance of biosurfactants, sugar based alkyl glycosides and sophorolipid esters as reagents to control the hydrophobicity of minerals with selectivity of adsorption on mineral surfaces for flotation applications. It was discovered that n-dodecyl-ß-D-maltoside adsorbs on alumina, titania and hematite but, interestingly, not on silica. The hydrophobicity obtained is governed both by the surface coverage as well as the nanostructure of the adsorbed layer in terms of orientation of the adsorbed species. Surprisingly, even though the above surfactants are non-ionic, their adsorption was pH-dependent. We have correlated this pH dependence to the type of species on the mineral surface. Also it is shown that mixing of these surfactants with traditional ones can help reduce the carbon footprint due to synergy between the reagents and help selectivity due to antagonism. The experimental results were analyzed to get information on optimal pH and dosage conditions, for mineral surface modification. The study provides guidance for mineral treatments using biosurfactants and the potential use of these next generation reagents in mineral processing.

Jan 1, 2014

By Aline Tavares

This paper describes the investigative studies carried out at Vale´s Center of Mineral Development (CDM) for a nickel sulfide deposit aiming to develop an adequate flotation flowsheet. The CDM facilities comprises of very well equipped laboratories to develop hydrometallurgical, comminution, flotation, physical separation processes, besides chemical and mineralogical laboratories, that are required to accomplish pre-feasibility studies, new process routes developments and, eventually, brownfield projects. Close association of the flotation group with the geometallurgy and the mineralogy teams play a key role during greenfield project development. Most of the information required by process engineers responsible for the flowsheet development can be provided by the mineralogy team and its mineralogical laboratory at CDM. During the flowsheet development of this nickel sulfide deposit, two ore types were identified as the most abundant in the deposit, named biotite-chlorite hydrothermalite (HID) and magnetite hydrothermalite (MAG HID). Six samples were selected for the investigative studies based on this initial information. Nickel grade varied from 0.39% to 1.95%. The main nickel-bearing minerals were millerite and pentlandite whereas the main non-sulphide gangue minerals were quartz, plagioclase, biotite, chlorite, actinolite, and/or magnetite. Electron microprobe (EMP) identified the presence of nickel in solid solution in gangue minerals such as biotite, chlorite, and actinolite. Nickel deportment in silicates varied from 3% to almost 40%. Magnesium was distributed in biotite and chlorite, except in sample MAG HID, in which talc was responsible for almost 50% of the Mg content. Liberation studies indicated that the optimum feed grind size was around 150µm and that pyrite occurred highly associated to the nickel sulfides. The flotation tests were planned based on the information provided by the mineralogical data. Rougher flotation tests indicated that the optimum P80 of the primary grind was 212µm for the HID type and 150µm for the MAG HID. From the reagents tested, amyl xanthate proved to be the most efficient in the recovery of the sulfides. In the MAG HID sample talc was well depressed by dosing 600g/t of CMC. Nickel recoveries in the rougher stage were lower than 90% due to the nickel distributed in silicates. However, sulfur recovery was around 95%, indicating high recovery of the total sulfides. Open circuit and locked cycle tests were conducted to evaluate the effect of the regrind size in the nickel grade and recovery (P80 of 44µm and 20µm). Nickel recovery decreased from 70% to 65% when finer regrind size was tested. Although nickel recovery decreased by 5%, the finer regrind size lead to a higher Ni grade (from 11% to 23%Ni) and lower fluorine grade (from 1138ppm to 700ppm) in the concentrate. Keywords: nickel sulfide, flotation, mineralogical characterization, flowsheet development

Sep 1, 2012

By Y. G. Sun

This paper mainly reported separation manganese silver oxidized ores process by amylum de-gradation reduction and its influencing factors. When dosage is given according to nMn : nH2SO4 : n(C6H10O5)n : nH2O=1:k21.8: k116.66:30, the amount of up to 95.93% Mn leach rate and less than 2% silver loss can be obtained. Cyanidation process was used to extracted silver from leaching Mn residues. Silver leach rate could reach 94.15% at consumed amount of 1kg/t NaCN for 1h. Silver leach recovery rate was more than 92.27% by leaching Mn and cyanidation two-step processes so manganese and silver were separated effectively.

Jan 1, 2014

By Y. F. Guo

Among the different valences of vanadium, V (?) is insoluble in acid, V (?) and V (?) is in-soluble in water but soluble in acid. Vanadium mainly exists as V (?) in vanadium titanium-rich material obtained by reduction -milling-separation from vanadiferous titanomagnetite. Therefore, the vanadium titanium-rich material can not be used to extract vanadium by acid directly. In this paper, the vanadium leaching was studied by oxidation roasting and acid leaching. Through oxidation roasting, vanadium is transformed from the insoluble V (?) into V (?) or V (?) in order to improve the leaching of vanadium. The results show that vanadium leaching increases significantly by oxidation roasting-acid leaching. Leaching of vanadium is up to 70.18% under the optimized conditions of roasting temperature of 950 ?, roasting time of 40 min, sulfuric acid concentration of 40%, leaching time of 4h, leaching temperature of 95 ? and liquid to solid ratio of 4 : 1.

Jan 1, 2014

By J. K. Wen

The Mojiang nickel deposit is situated in Mojiang county, yunnan province, a tropical area in the southwestern China. The known geological resource (measured and inferred) includes 4 million tons of nickel sulphide ore at an average grade of 0.50% Ni and 0.34% As. Nickel minerals are mainly gersdorffite (NiAsS), millerite(NiS), morenosite (NiSO4?7H2O), and more than 50% nickel minerals is gersdorffite which contains arsenic. Pyrite is the dominant sulfide mineral, 22% in the ore and part of nickel minerals are locked in pyrite. It is difficult to attain the nickel concentrate quality allowed by a smelter and the acceptable nickel recovery through flotation due to the high arsenic in the ore and the nickel minerals locked in pyrite. The shake flask tests and column tests for nickel recovery from the Mojiang nickel sulfide ore had been finished by the end of 2003. The column bioleaching tests were carried out using the columns with diameter of 120 mm and height of 1200 mm, and 70% of nickel dissolution was attained in 300 days. A 10,000t pilot test heap was built in the Mojiang Nickel Mine by June 2003. The ore used in the test heap was supplied from the underground mine and was crushed to -20 mm before being feeding to the test heap, which is 4~5 m high, 30 m wide and 50 m long. The naturally adapted mesophile and moderate thermophile have been inoculated into the leaching pile by June 2003. The operating temperature in the heap ranges from 38? to 55?, varying with season. 30% of nickel dissolution was achieved in 3 months and the typical pregnant leach so-lution (PLS) contains 2~3 g/L Ni and 20~30 g/L Fe. The Ni sulfide which was produced by us-ing Na2S 10 t/t?Ni contains 16%~20% Ni and Ni recovery was 98%. 70% of Ni dissolution is expected in 12 months. The test heap was scaled up to 60,000 t of ore per year by mid of 2005. In this paper metallurgical studies and performance of the pilot test heap will be described. The results of mineralogy, shake flask tests and column tests on bioleaching of the nickel sulfide ore are reviewed. The key test heap operation parameters, the performance of bio-heap leahing-Na2S precipitation, ferrous oxidation-ferric precipitation-Na2CO3 precipitation, bacteria in the pile, water and acid balance, effluent disposal, capital and operation costs are also discussed.

Jan 1, 2014

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 Genrich A. Denisov

Principles of ecologically friendly geo-technologies construction are formulated on the basis of the works of the leading scientists in the field of rational processing of mineral resources of the Russian Academy of Sciences. One of these concepts is a new direction in rotational disintegration of mineral and technogenic raw material with the purpose of effective subsequent enrichment. A large amount of practical experience has been accumulated in the industry on selective destruction by application of vibrational method on initial material with consideration of its physical-mechanical properties and mineral structure. This method is successfully realised in a conic inertial pulverisation devices constructed by Mekhanobr Institute (St.-Petersburg). A new construction of conical-inertial pulverisation with a modification of disintegration force has been developed recently at Mekhanobr Institute. It allows, in some cases, to increase selectivity of subdivision and to avoid over-disintegration. Advantages of “wet” subdivision methods in conic inertial disintegration devices are proved. The efficiency of such subdivision can be increased due to rational use of the phenomenon of a dislocation-dynamic diffusion. Its advantage is proved by the effect on disintegrated material by frequency-modulated variable electrical fields of low power. It was shown in industrial conditions, that the productivity of the spherical mill can be increased by 10 %, and that it also prevents ecologically harmful surface active substances (SAS) in milling zone and it reduces the dust content in the air. The techniques of tentative estimation of efficiency of various proceedings technogenic materials and their classification are created. The scientific fundaments of rational, ecologically friendly technology of processing and regeneration of various kinds of technogenic raw material are developed. A number of effective technologies on processing of wastes is developed and inculcated in concentration factories and metallurgical factories.

Jan 1, 2003

By Dingwu Feng, Jannie S. J. van Devente

"The effect of ultrasonication on reactions at solid/liquid interfaces was investigated in two slurry systems, i.e. gold cyanidation and geopolymerisation. The kinetics of gold extraction were significantly enhanced and the cyanide consumption was reduced in the cyanidation of a pyrite concentrate using ultrasonication, probably due to the prevention of leaching passivation, the improvement of the dissolution of the gold host sulphides and the oxidation of soluble sulphides to sulphate. The effectiveness for ultrasonication was improved with the injection of oxygen and the addition of dithiophosphate through enhancing the formation of the oxidation radicals and selectively inducing cavitation bubbles directly at the sulphide interfaces. Ultrasonically enhanced cyanidation could render currently uneconomic deposits viable for extraction by improved cavitation efficiency with the aid of surfactants.Ultrasonication increased the compressive strength of the formed geopolymers through accelerating the dissolution of the Al-Si materials, strengthening the bonds at the solid particle/gel phase interfaces, enhancing the polycondensation process and improving the formation of semi-crystalline to crystalline phases. The use of power ultrasound will yield high-performance geopolymer materials."

Jan 1, 2003

By Glasswell K. Nkonde, Fredrick Chileshe, Steven Simukanga

Improving food security by increasing crop output is a primary objective for most countries in the sub- Saharan region. Most soils in the region are deficient in phosphorus an important nutrient after nitrogen in plant growth. Phosphates are therefore used together with nitrogen and potassium based fertilizers in improving crop production. Zambia like many other countries in the sub-Saharan region imports phosphate fertilizers for use by its farmers. However, indigenous phosphate deposits of igneous origin exist in Zambia of which the main ones are Chilembwe in Petauke district, Mumbwa sugarloaf in Mumbwa district, and Nkombwa Hill in Isoka district. If commercially exploited, these deposits could become a ready source of inexpensive phosphate for the local farming communities in the country. Previous research has shown that partially acidulated phosphate rock (PAPR) produced using Chilembwe phosphate rock is just as agronomically effective as the imported superphosphate fertilizers on food crops in most of the Zambian soils. PAPR is produced by reacting finely ground phosphate rock with only a fraction (usually 50%) of the stoichiometric quantity of the sulphuric acid required to fully convert the apatite in the rock to monocalcium phosphate thus making the process cheaper in terms of acid consumption than the poduction of single superphosphate where the apatite in the rock has to be fully converted to monocalcium phophate. The factors that affect the percentage of available P2O5 in the PAPR produced include particle size of phosphate rock, degree of acidulation, concentration of acid, process temperature profile, residence time and drying temperature. These factors were studied in a 25kg/hr PAPR pilot-plant in the School of Mines at the University of Zambia using Chilembwe phosphate rock. The PAPR pilot-plant consisted of a rotary drum granulator as the main reactor, a rotary drum dryer and a triple deck vibrating screen. Ground phosphate rock was reacted with sulphuric acid and water in the granulator to form a granular product which entered the drier. The dry product was screened into three size fractions. The 1 – 4 mm size fraction was the final product whilst the –1mm size fraction was recycled. The +4mm size fraction was sent to a crusher while the crushed PAPR was sent back to the screens.

Jan 1, 2003

By Zhazira Baltabekova, Nina Lokhova, Arailym Dukembayeva, Madali Naimanbayev, Zhantore Dzhurkanov

"Recycling of industrial waste provided they have enough valuable elements requires significantly less investment compared with ore processing. Promising man-made raw material of rare earth elements (REE) is phosphogypsum. Works performed on dismantlement of phosphogypsum only concern phosphogypsum processing from apatit. In this case, none of the developments was tested for phosphogypsum produced on the basis of phosphorus, chemical and mineralogical composition of which is markedly different from apatites. We studied phosphorites of the Karatau deposits (Kazakhstan). Mineralogically all the layers are composed of three main ingredients: phosphate, silica and carbonate, which account for 92-96% of the weight composition of ores and rocks. Of impurities there are pyrite, iron hydroxides, gypsum, fluorite. In addition to the actual composition of phosphate in phosphate ores there are apatite. Silica is presented by chalcedony and quartz, and carbonate by calcite and dolomite. The results of X-ray microanalysis showed point cluster of grains containing REE in samples of phosphate ore. Analysis of the grain showed that REE are in the form of phosphates and silicates, which according to numerous studies in apatites is not established. In this regard, phosphogypsum, waste of production, is different in composition too. Therefore, transfer of techniques proposed in the methods for extracting REE from phosphogypsum after processing apatite, did not give the stated results and required a new approach to solving this problem. It should be noted that the phosphogypsum produced by processing the Karatau phosphorite contains medium group of REE by 2.6, and heavy group by 7.8 times more than phosphogypsum from processing the Kola apatite. Given the shortage of medium and heavy REE research to develop ways to extract the lanthanides from phosphogypsum after processing phosphate rock is promising. The study contains results of studies on the extraction of REE from phosphogypsum after Karatau phosphorite processing."

Jan 1, 2014

By Richter, E. Charikinya

"Mineral processing unit models require information on particulate properties such as particle size, solids flowrate and mineralogical composition to model their operations. Process models that describe the separation process can be classified based on the level of information required from the ore, i.e. the feed stream to the separating unit. The most comprehensive level of mineral processing models is the particle-based modelling approach. Particle based modelling describes a modelling approach where mineral composition, mineral liberation and textural information of particles making up the process streams is used in modelling. The advantage of this approach is that all model streams carry particle level information (size, liberation, shape). This information is obtained by applying automated mineralogy techniques such as Quantitative Evaluation of Minerals by Scanning Electron Microscopy (QEMSCAN) analysis which provide accurate and detailed information on process stream particle properties. Currently the use of liberation information in modelling and simulation is rare, due to the limited number of separation models that liberation data as input. The objective of this study is to develop a particle based model for a dry magnetic separator, where mineralogical information is used directly to simulate a dry magnetic separator operation. Magnetic separation tests were carried out on high, medium and low grade magnetite ores using a laboratory magnetic separator. Streams from the separator were sampled and sized for chemical and liberation analyses. A sized mass and elemental balance around the magnetic separator was carried out. The elemental assays of each stream were converted to mineral quantities and a sized mineral balance was done. QEMSCAN measured liberation data was reconciled to the mineral balance based on mineral quantities obtained from chemical assays. This was followed by the development of a particle based model that calculates the trajectory of a single particle based on its mineral composition and textural properties. The model was tested on experimental data and was able to predict the effect of variation in process feed stream mineralogical attributes (liberation, grade, particle size) on magnetic separation performance. Results of this study highlight the benefits of the particle based modelling approach. INTRODUCTION The extraction of mineral values from ore requires liberation of the value minerals from the gangue followed by their separation. Liberation is achieved by size reduction operations (Desmond, 2008; Fuerstenau and Abouzeid, 2002). Separation of gangue material from value mineral takes place in various mineral upgrading stages such as classification, magnetic separation and flotation. In these concentration stages value minerals are separated from gangue minerals based on the physical properties of the ore particles making up the feed such as size, liberation, volume of magnetic material and density. The success of separation is related to the liberation of the feed particles, the performance of the separation technology applied, as well as the inherent characteristics of the feed material (Leißner et al., 2013)."

Jan 1, 2018

By Mohan Ram

Structural impurities in the crystal lattice of rock phosphate of Indian origin is a great challenge for beneficiation and practically possesses remote scope of upgradation to the desired level for industrial utilization. There is a wide occurrence of rock phosphate in different parts of India with different characteristics viz. siliceous, carbonaceous and ferruginous. The structural cationic replacement in the composition of apatite is due to the exchangeable cations present in the external impurities associated with the rock phosphate ore. The Indian rock phosphate ore from Purulia district, West Bengal is characterized as unusual structural composition due to the exchangeable cation in its composition. The elemental distribution of ore exhibits the disproportionate ratio of P2O5 and CaO which is 5.88: 3.31 in reference to the theoretical composition of P2O5: CaO in apatite which is 4.23: 5.55. The substitution by trivalent Al+++ cations within the structure of apatite in place of divalent Ca++ is found upto 18% and substitution of exchangeable cation in place of PO4 and F ion by CO3/SO4 is found upto 0.1% and OH ions upto 0.2% respectively in a lattice of apatite thereby diluting the grade of rock phosphate and restricting its industrial use even after beneficiation. This paper reveals the unusual compositional features of rock phosphate under study and is a guideline to the mineral industries using such rock phosphate. Keywords: external impurities, exchangeable cation substitution, structural compositional features, electron probe micro analyzer

Sep 1, 2012

By S. V. Volkova, S. V. Mamonov, T. P. Dresvyakyna

"The purpose of the work is complex processing of sulphide-magnetite ores with the separation of iron into iron concentrate, copper and noble metals into copper concentrate.The work shows the research results of the material composition of the sulfide-magnetite ore in the South part of the Peschanskoye deposit. According to the research results it is found that ore contains 0.59% of copper, 66% of which is related to chalcopyrite; 39.9% of iron, 81% of which is magnetite and 3.87% is sulfur, 42% of which is associated with pyrrhotite, 65% of which is a monoclinic modification. According to the results of the mineralogical analysis, it is found that the main iron-containing mineral in the ore under study is magnetite, the content of which is 45%. In addition to magnetite, iron is found in carbonates, pyroxenes, amphiboles, chalcopyrite, pyrrhotite and pyrite. The main copper mineral in the sample is chalcopyrite; covellite, chalcosine, bornite have a subordinate value. The total content of copper minerals in the sample is about 1%. The processing technology provides the three-stage grinding of the ore to a size of 65% of the class-71 µm; a cycle of copper flotation; a cycle of pyrrhotite flotation; wet magnetic separation of flotation hosts. The following optimal parameters are established for the ore under study: the alkalinity of the slurry is 250-280 g/m3 of free calcium oxide in the liquid phase of the slurry; the duration of the main copper flotation is 20 min; the consumption of butyl potassium xanthate is 20 g/t; the consumption of the foam generator T-92 is 15 g/t; the consumption of copper sulfate for the activation of pyrrhotite is 300 g/t; the magnetic field strength is 1500 Oersteds.A complex flotation-magnetic technology for the enrichment of sulfide-magnetite ore has been developed in the laboratory in order to produce a copper concentrate containing 21.6% of copper with 91.7% extraction and an iron concentrate with 66.5% of iron mass fraction and 1.2% of sulfur with an extraction of iron into the concentrate of 87.9%."

Jan 1, 2018

By A. K. Majumder

In an effort to test the extent to which fundamental fluid mechanics can provide a prediction of particle separation, a study on a simple parallel-sided sluice has been carried out using glass bead and ilmenite mixtures at various particle concentrations and flow rates. Great care was taken to devise a flow splitter at the end of the sluice that permitted accurate measurement of the fluid flow profile and collection of slurry samples, allowing evaluation of the particle species concentration profiles. The actual particle separation taking place was compared to predictions made by first describing the fluid flow by a modified ?law of the wall? model. The hydrostatic pressure variation in the flow was taken into account and the eddy viscosity was calculated from a mixing length expression incorporating Van Driest?s damping function. Using an average density and viscosity provides an explicit expression for the velocity gradient that can be numerically integrated for the flow profile. The particle concentration distributions were then modelled with Hunt?s sediment transport model assuming the particle eddy diffusion coefficient to be the same as that for the water. Hindered settling velocities of the particles were calculated using Brauer and Thiele?s formula, which takes the particle size and density distributions and solids volumetric concentration into account. The resulting predictions of particle separation are shown to be a strong function of the settling velocities of the particles used. Keywords: flowing film concentrators, fluid velocity

Sep 1, 2012

By R. Singh

The present paper deals with the development of flotation based process for enrichment of a lead-zinc sulphide ore from Ganesh-Himal region of Nepal. Detailed characterisation and flotation studies were carried out under varying process conditions. The sample assayed 2.47% Pb with 13.6% Zn. The ore was predominantly made up of spahlerite and pyrite in association with subordinate amounts of galena, minor amounts of pyrrhotite and chalcopyrite. Dolomite was the main gangue. The modal analysis showed the probability of fair liberation of sulphides from gangues around 210 microns but the locking of galena with sphalerite and other sulphides continued to finer sizes. Under the optimum process conditions the rougher lead and zinc recoveries were 96.3% and 90% respectively. Multistage cleanings of rougher products proved helpful in improving the concentrate grade, meeting the required specification. Based on the studies undertake a process flow-sheet for the concentration of the ore to individual lead and zinc concentrates was developed.

Jan 1, 2014

By ?. Kostadinov

Theoretical study of the behavior of grinding medium presented by TBP (tetraballpebs) was conducted by computer modeling of the position of grinding medium at different speeds and different drum fill factor. For the modeling were used known equations of motion derived for the ball load. Algorithm was created by SolidWorks software, allowing determination of center of gravity of the load in the mill and energy for grinding. These results were compared with similar results obtained by ball grinding medium. The capabilities of both grinding media are demonstrated by graphics under the following conditions: 1.Equal dimensions of the experimental model of the mill; 2.Equal mass of the grinding loads; 3.Comparison of grinding bodies with the same number, mass and density. Keywords: simulation, behavior, grinding medium, balls, tetraballpebs

Sep 1, 2012

By Evvie Chockalingam

Acid mine drainage (AMD) is a perennial problem particularly in abandoned mines, occurring due to the oxidation of sulphidic mine wastes. AMD is usually characterized by high concentration of dissolved metal ions, sulphate and low pH. The efficacies of substrates such as rice husk and the bark of Eucalyptus tereticornis (Sm.) are assessed for the removal of metal ions such as iron, zinc and copper from acid mine water obtained from an abandoned copper mine. Over 99 % of Fe, 98 % of Zn and 95 % of Cu removal could be achieved from acid mine water, with a concomitant increase in the pH value by three units using rice husk as an adsorbent. With respect to tree bark as an adsor-bent, about 96 % of Fe, 75 % of Zn and 92 % of Cu could be removed from the acid mine water with an attendant increase in the pH value by two units. The free energy of adsorption of the metal ions onto rice husk and tree bark is found to be negative in both the cases, while the adsorption process is endothermic in the case of rice husk and exothermic for tree bark. The adsorption process is found to adhere to the Lagergren pseudo-first order rate equation. The reduction of sulphate con-centration in the acid mine water is achieved using a typical sulphate reducing bacteria namely De-sulfotomaculum nigrificans. Desorption experiments indicate that about 88 % of Zn, 87% of Cu and over 77 % of Fe could be recovered from rice husk and over 70 % of Fe, 82 % of Zn and 77 % of Cu could be desorbed from the metal loaded tree bark using 5 M HCl. The possible mechanisms of metal ion and sulphate removal from acid mine water using rice husk and tree bark are discussed.

Jan 1, 2014

By Arman Ehsani, Ersin Yazici, Haci Deveci

The downstream treatment of chloride leach solutions of WPCB for recovery of base and precious metals by a combination of adsorption and precipitation processes were carried out. A synthetic leach solution (1 M HCl, 116.5 g/L Cl-, 30 g/L Cu2+, 2.5 g/L Fe3+, 5 mg/L Au3+, 10 mg/L Ag+ and 20 mg/L Pd2+), which was prepared based on the composition of the pregnant leach solution obtained in the previous study was used in the tests. The leach solution was initially subjected to activated carbon (AC) adsorption (20 g/L AC, 80°C) in which gold was selectively recovered over silver and palladium i.e., 88% Au recovery at 0.5 h (92% at 3.5 h) compared with only 3-6% for Ag/Pd. Copper and iron were also observed to adsorb on AC as indicated by 1.4% and 17% decline, in their respective concentrations. Following the adsorption and filtration stage, metallic copper was added into the gold-barren solution to allow reduction of Cu2+ to Cu+, and to cement Pd on metallic copper. Over the mixing period (1 h), 93% of the Pd was recovered while only 1.4% of silver was cemented onto metallic copper. Subsequently, the leach solution was gradually neutralised by NaOH to pH 4, 7.5 and 9.5 for the precipitation of copper as cuprite (Cu2O). It was found that 41% and 46% of Cu and Ag, respectively, were precipitated at pH 4 at which iron was almost totally (99.8%) removed from solution. Precipitation of copper and silver was increased further at high pHs. At pH 9.5, cumulative recoveries for copper and silver were 91% and 85%, respectively. XRD analysis of the precipitates confirmed the presence of cupric copper oxides/hydroxides and revealed that copper losses occurred at pH 4 was due to the undesired presence of cupric copper in the solution.

Jan 1, 2014

By Masakazu Niinae, Tasuma Suzuki, Mai Moribe, Yohhei Okabe

Bench-scale electrokinetic experiments were performed to elucidate the electrokinetic remediation mechanisms of arsenate from artificially contaminated kaolinite. The electrokinetic experiments in which a constant voltage was applied demonstrated that high soil pH favored arsenate remediation with respect to both the remediation time and electricity consumption. It was also demonstrated that applying a pulse voltage (1 hour ON, 1 hour OFF) significantly improved the electricity consumption efficiency when the soil pH was maintained at the initial value during the experiments; this trend was not observed when the soil pH was gradually increased from the cathode side. These electrokinetic experimental results indicate that the remediation rate-limiting step varied with soil pH. When the soil pH was maintained at the initial value of 7.2 during the experiments, arsenate desorption was the remediation rate-limiting step rather than the migration of dissolved arsenate toward the anode. Conversely, when the cathode pH was not controlled and the soil pH was correspondingly increased gradually from the cathode side, the migration of hydroxyl and desorbed arsenate ions toward the anode played a more important role in the control of the overall remediation efficiency.

Jan 1, 2014

By L. G. Schumskaya, ?. S. Yusupov, ?. ?. Kirillova

"It has been shown on the example of cassiterite that grinding in mills of the increased power lead to destruction of the fine crystal structure and consequently to change in physical and chemical properties of the mineral, that is its transition into mechanically activated state. The increase in mineral reactivity is related to both the growth of mineral specific surface and sharp decrease in the sizes of primary crystallites accompanied by essential increase in number of microdefects that is clearly expressed in its increasing solubility during interaction with corrosive mediums, especially with acids. Calorimetric measurements indicate that the thermal effect of SnO2 solubility increases considerably.These observations allow us to propose two techniques of hydrometallurgical treatment of cassiterite: direct dissolution of the mechanically activated mineral in acids, although it is a very power-consuming process, and mechanical activation of cassiterite in presence of metals that are able to release hydrogen from acids. Active hydrogen is released during interaction between the mechanical mixture of SnO2 and metal with acids and reduces tin from the mineral transferring it into solution.In addition to other technological properties, the flotability of cassiterite has been thoroughly studied. It has been found that it steadily decreases as activation proceeds because of increase in the degree of hydratability of particle’s surface. In this case, the mechanical activation is provided through tribotreatment of a surface rather than through fine grinding. On this basis we developed the technique of inverse cassiterite flotation with its subsequent transfer into a chamber product that considerably increase the quality of a tin concentrate.The observed technological effects may be generally explained by occurrence of the valenceundersaturated, strained (deformed) chemical bonds and other active centers on the cassiterite surface while decrease in its flotability - by formation of the hydrolyzed tin species and impurity iron, such as Sn(??)4°, Fe(??)2 +, Fe(??)3° hydroxocomplexes and others."

Jan 1, 2003