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By Kaiwen Liu

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

Sep 1, 2012

By Çisem Tuba, Ismail Girgin

"Comparative atmospheric H2SO4 and H2SO4 + H2O2 leaching experiments were performed using a Turkish lateritic nickel ore containing 1.52% Ni. In the leaching tests; acid concentration, temperature and leaching time were considered as main variables and the dissolution behaviour of the ore were studied by Ni, Fe, Co and Mg analyses. The dissolution values in the H2SO4 leaching experiments were observed to increase up to 60% (w/w) acid concentration and a temperature of 95°C. Increase of H2SO4 concentration above 60% at 95°C caused decreases in all the dissolution values and this was attributed to the formation of Fe2(SO4)3 and Fe2(SO4)3•HSO4•H2O type compounds. At the considered optimum H2SO4 leaching conditions ([H2SO4]= 45%, T=95°C, t=45 min); dissolution values reached for Mg, Ni, Fe and Co were determined as 99.12%, 95.58%, 92.63% and 78.37%, respectively. An activation energy of 30.57 kJ/mole was determined for nickel dissolution from the evaluation of the kinetic data obtained for H2SO4 leaching showing that the dissolution was controlled by external diffusion and chemical reactions. Caro’s acid solutions were prepared at H2SO4/H2O2 mole ratio of 3 for varying initial H2SO4 concentrations and leaching tests were performed at 25°C. Co behaved very differently and a dissolution value of 83.94% was obtained even at 5% acid concentration in 60 minutes reaction time. Complete dissolution of Co was obtained after 30 minutes of reaction time at 60% initial H2SO4 concentration and the corresponding dissolution values for Mg, Ni, and Fe were reached to 96.16%, 94.27% and 89.46%, respectively. Although the H2SO4 + H2O2 leaching experiments were conducted at 25°C, it was realized that the temperature of the leaching medium was increased to 122°C after four minutes of reaction time due to probable exothermic reaction(s) at 60% initial acid concentration."

Jan 1, 2014

By Güven Önal, Zeki Dogan, Neset Acarkan

In this study, it was aimed to produce glass sand with less than 0.15% Fe2O3 for window glass manufacture and glass ware grade with less than 0.05% Fe2O3 from Yalõköy sand dunes having 0.48% Fe2O3. In order to reduce the iron content of the Yalõköy sand dune, magnetic separation, flotation, scrubbing, H2SO4 leaching and drying were used. The optimum iron removal was achieved by H2SO4 baking at 150oC and 8 kg/t acid consumption. In this way, sand concentrate was obtained with 0.04% Fe2O3 and sand recovery 95%.

Jan 1, 2003

By Markus A. Reuter, Albert Scholte, Ewoud V. Verhoef, Gerard P. J. Dijkema

A dynamic, interactive map has been developed of the life cycle of a number of metals, from mining through to minerals processing, metal production, product manufacturing, recovery and waste management. Whilst the existing metal process network and waste management infrastructure provide substantial scope for (product) design, these also limit change due to the complex interdependence of metals, both in production and recovery, and the strong path dependency of industry and infrastructure development. Therefore, models for dynamic simulation were constructed that allow the specification and evaluation of the metal process network and waste management infrastructure ‘products’ over a longer time span. The model has been constructed using a bottom-up approach, to enable assessment of the environmental aspects of metallurgy and to simulate changes in the system structure and technology, i.e. from reactor or individual process step up to integrated material cycles. The model comprises hierarchical mass balances and linear models of individual processes and sub-processes. Thus, at lower system aggregate levels an increasing level of technical detail is represented. Data reconciliation has been used literature data on process feed, products and residue composition to calculate representative and reliable split factors around each (sub-)process. World production figures on process capacity and recovery rates are be used to calculate the relative contribution of processes. The dynamic map is illustrated with a case on the introduction of lead-free solder.

Jan 1, 2003

By Erico Tabosa, Meng. Jun, Kym Runge, Matthew Brennan, Weiguo Xie, Dee Bradshaw

Turbulence and its distribution are of great importance in flotation cell design as they affect suspension of particles, air dispersion and particle-bubble collision rates, which in turn determine flotation performance. However, there is no mature technique to measure turbulence in three phase (liquid-solid-gas) systems such as in flotation cells. In this article, the authors present two new approaches that are suitable for measuring turbulence distribution in three phase systems and validate their applicability. The first technique uses a piezoelectric vibration sensor (PVS) to measure fluid kinetic energy standard deviation and the second technique applies electrical resistance tomography (ERT) to measure conductivity variation at a measurement position in a flotation cell. For the PVS technique, calibration of the sensor was performed to determine the values of parameters that were needed to calculate the force applied to the sensor. Then measurement was conducted in a 60L batch flotation cell and the results were compared with LDA measurement. This demonstrated that the piezoelectric sensor signal provides a good representation of fluid kinetic energy standard deviation at the position of measurement. For the ERT technique, conductivity distribution data was processed to give conductivity variations, which were then used to calculate fluid kinetic energy standard deviation at the measurement position. The spatial distribution of turbulence obtained by performing multiple measurements at different positions in the 60 litre batch flotation cell was found to agree with the PVS measurement results. These two techniques are potentially powerful tools for turbulence measurement in flotation environments, enabling a clearer understanding of turbulence’s influence on flotation performance to be determined.

Jan 1, 2014

By I. Zh. Bunin, G. K. Khachatryan, N. E. Anashkina

For optimization of diamond processing technology the influence of nanosecond high voltage pulses on mechanical and technological properties of diamond crystals and kimberlite rock-forming minerals (calcite, olivine, serpentine) was investigated. Using methods of Fourier Transform Infrared Spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), microscopy and mikrohardness measurement the changes of structural, physic-chemical surface properties, and microhardness of minerals as the result of impacts, was studied. Non-thermal impacts caused a decrease of kimberlite rock-forming minerals microhardness in general to 40-66% as the result of surface microstructure destruction which is caused by formation of micro cracks, traces of surface breakdown and other defects. At the same time, the pulse energy impact on natural diamonds led to formation of B2 type crystal lattice microsift defects, elevated concentration of which increases the hardness properties of crystals. The obtained result indicates possibility of applying pulsed energy effects to improve the softening efficiency of diamond-bearing kimberlites rock-forming minerals without damaging the diamond crystals and ensuring their preservation by the subsequent grinding of ores. By IR and X-ray photoelectron spectroscopy revealed that processing by hight voltage pulses causes a change of natural and synthetic diamonds surface functional cover composition. Short-term exposure (~ 10 - 30) leads to detachment and partial destruction of secondary phases mineral films on the surface of natural technical diamonds, increasing floatability and hydrophobicity of crystals. However, with increasing duration of treatment (~ 30 - 150) occurs surface hydroxylation (found by XPS for synthetic diamonds), as a result of diamond surface layer oxidation. The effect of increasing the natural diamonds flotation activity by 14% (from 47% to 61%) was experimentally established as a result of processing diamond crystals with nanosecond pulses (~ 10-50 sec), which indicates the principal possibility of using pulsed energy impacts to intensify the diamond flotation during processing diamond-bearing kimberlites.

Jan 1, 2018

By E. V. Manlapig

"Some researchers postulate that the floatability of a particle in the streams of an industrial flotation circuit is a function of only its size and liberation properties. They do not discount the importance of reagent or surface contamination on particle floatability but assume that the reagent coverage or surface contamination of the particle surfaces is essentially uniform for particles of similar size and mineralogical properties when subjected to a particular chemical regime.In this paper, samples collected from laboratory batch flotation tests performed on different streams of Cominco Teck’s Red Dog lead cleaning circuit have been characterised with respect to their size, mineral association and mineral surface exposure. An analysis of this data set indicates that the flotation rate of a particle in an industrial flotation environment is a strong function of its size and also of the mineral composition of its surface (Figure 1). It is a function not only of the proportion of the most floatable mineral on its surface but of the floatability of the other minerals on its surface as well.Nodal analysis is a technique developed by the authors that can be used to determine if the ore floatability of a particle class is changing within an industrial flotation circuit. This technique is used within the paper to show that the floatability of all the different types of particle classes studied within the Red Dog circuit did not change significantly during the lead cleaning stage. However, it was also concluded that particles with the same size and mineral composition did not all float with the same rate in the individual streams of the flotation circuit, but with a distribution of rates. It is suspected that the particles within a size mineralogical class in this study have varying degrees of surface oxidation and that this results in varying particle flotation rates. Thus basing particle floatability on size and mineralogical effects, alone, in a flotation model is not always valid."

Jan 1, 2003

By Alejandro Uribe-Salas, Fabiola Nava-Alonso, Gloria Dávila-Pulido

This paper presents results of an experimental study performed on the role of calcium sulfate present in flotation water on sphalerite flotation in the Pb/Cu circuit (non Cu-activated sphalerite) and in the Zn circuit (Cu-activated sphalerite). In the Pb/Cu circuit calcium ions adsorb on the negatively-charged sphalerite favoring xanthate adsorption and therefore making sphalerite floatable; experimental measurements show sphalerite contact angle increases with calcium concentration while xanthate adsorption onto sphalerite increases with the increase of pH and calcium concentration. Gypsum (CaSO4·2H2O) eventually present due to calcium sulfate precipitation is not detrimental to flotation at this stage since it is negatively charged at pH 9 and therefore, does not adhere onto the surface of negatively-charged sphalerite. In the zinc circuit, Cu-activated sphalerite decreases its negative charge (or even becomes positively charged) and develops some hydrophobicity due to the polysulfide produced by Cu-activation. At this stage calcium ions do not interact with the mineral surface and therefore do not favor xanthate adsorption; nevertheless, precipitated gypsum particles do adhere onto the mineral surface, greatly affecting its floatability (e.g., contact angle). Addition of sodium carbonate to dissolve gypsum and to precipitate calcium as calcium carbonate, which disperses in the bulk of the suspension, effectively restores mineral hydrophobicity. SEM observations coupled with EDS analysis clearly illustrate and support the above sequence of events.

Jan 1, 2014

By C. Dorfling, S. Bradshaw, J. Eksteen, M. Khesa, C. A. Snyders

Titaniferous ores serve as a major feedstock for the production of a white titanium dioxide pigment, a titanium metal and several other titanium-based products. Such ores exist mainly as heavy mineral sands. Ilmenite is upgraded to intermediate products namely synthetic rutile and titania slag through the synthetic rutile route and the reductive smelting route respectively. Tronox KwaZulu Natal Sands (Pty) Ltd recovers high titania slag via the reductive smelting process while slag is used as a feedstock to the pigment industry and furnace dust from the gas cleaning plant is disposed as waste. Previous investigations have shown that such furnace dust can contain significant amount of titanium-bearing minerals. This study looks at the characteristics of the furnace dust obtained from Tronox KwaZulu Natal Sands and investigates a possible high temperature recovery route in detail. The furnace dust was examined by using x-ray fluorescence, x-ray diffraction, microscopy and laser-diffraction size analyses. The characterization work showed that the furnace dust was rich in titanium and iron, containing 49.4 wt% ??????2 and 29.5 wt% ????2??3. These oxides were associated with Si, Mn, K, and Al oxides as impurities. A Carbolite® vertical tube furnace was used to investigate the extent of formation of titania slag and metallic iron on a laboratory scale at 1500°C, 1600°C and 1650°C. The laboratory reduction tests revealed that the slag samples with an equivalent titanium dioxide content ranging from 70.9 -76.9 wt% at 1600°C and 1650°C could be obtained. The Fe content of the metallic iron samples produced ranged between 93.0 and 97.1 wt%. The experimental results were found to be in relatively good agreement with the FactSage simulations, both of which demonstrated the potential of producing a titania slag and a metallic iron from the furnace dust.

Jan 1, 2018

Pure camsellite samples were prepared through crushing, sorting and grinding the high-grade iron-containing camsellite ores from Fengcheng, Liaoning, China. The flotation behaviour of camsellite was studied via a systematic investigation of camsellite flotation re-covery changes as a function of choices and dosages of collectors and depressants at different slurry pH. The results showed that at pH 8.5 to 9.5, the recovery of camsellite reached the maximum at 90%~93.5% using dodecylamine as the collector, while under the same condition a recovery of 84%~86% could be achieved with sodium oleate. The adsorption of dodecylamine was not affected by the addition of sodium hexametaphosphate, but the adsorption of sodium oleate could be significantly depressed. This implied that sodium metahexaphosphate could be used as an effective depressant for the other associated minerals during the dodecylamine flotation of camsellite. When starch was used as the depressant, the flotation of camsellite by sodium oleate was almost completely depressed in the alkaline conditions. Significant depressions were also observed when calcium chloride was added in the camsellite-sodium oleate system. The higher the slurry pH is, the stronger the depression. Zeta potential measurements indicated that the flotation was mainly initiated by the electrostatic adsorption of the collector on camsellite. X-ray photoelectron spectrometer (XPS) analysis showed that the adsorption was originated from the electrostatic attraction between the N atom in dode-cylamine and B atom in camsellite. Dodecylamine had a higher coverage on the camsellite surface than sodium oleate.

Jan 1, 2014

By Wolfgang Öfner

Many technical processes also yield dusty residues which usually contain appreciable amounts of valuable matter. Often they also accumulate substances detrimental to the process. Dumping them entirely in landfills wastes raw material and causes high disposal costs, but recycling them without prior treatment is often not feasible. Physical separation processes are preferable because of their rather low energy demand. In order to develop such treatment systematically, the residues must be characterized properly. The technique for such a characterization is taken from mineral processing: perfect fractionation according to continuous properties of the particles supplemented with chemical analysis are used for plotting the Henry-Reinhardt chart. This represents the benchmark for assessing actual separation processes and tests. Their results are compared in terms of ?selectivity? and plotted in the kappa chart. In this paper, Henry-Reinhardt chart and kappa chart are applied to several different types of residues from iron and steel production and show their potential for being upgraded before reutilization in the production process. This approach is suitable for virtually all dusty residues from other industrial processes as well. Keywords: residue, dust,iron and steel, process development, Henry-Reinhardt chart, kappa chart

Sep 1, 2012

By J. Vilcáez

The copper extraction yield from thermophilic bioleaching of chalcopyrite depends on temperature, pH, and the oxidation-reduction potential (ORP), as well as the activity of the microbe used. We studied copper extraction yields obtained from chalcopyrite with three thermophiles, Acidianus brierleyi, Sulfolobus metallicus, and Metallosphaera sedula, under various pH and temperature conditions and with different initial amounts of ferric iron. The results indicated that the capacity of each thermophile strain to leach iron as Fe3+ differed, which affected the influence of pH, temperature, ORP, and microbial activity level on the yield of copper. Microbial activity can cause ORP to be close to the critical value (450 mV) at which copper extraction at 65 °C can be higher than that at 80°C. An initial pH of 1.5 retards the precipitation of jarosite, allowing temperatures as high as 80°C to result in copper extraction yields close to 100%. However, if a thermophile with a poor capacity to form Fe3+ is employed, 100% copper extractions can also be obtained at pH 2.5, because ORP is low as result of low amounts of Fe3+ in solution. Optimum temperatures for the growth of thermophiles did not always mean high copper extraction yields. Conversely, high biomass concentrations depending on the capacity of the thermophile strain to leach iron as Fe3+, can result in excess Fe3+ in solution, leading to the precipitation of large amounts of Fe3+ as jarosite. The bioleaching capacity of A. brierleyi was reduced or suppressed when insufficient initial Fe3+ was pro-vided to trigger the leaching reaction, whereas S. metallicus and M. sedula were less sensitive to the initial availability of Fe3+. This result confirmed that a direct enzymatic attack on the mineral surface could initiate the leaching reaction, but later ORP governed the leaching rate of chalcopyrite.

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 Aldo Cipriano, Fernando Estrada

The mining industry is in search of control strategies that allow considering a global optimization of their processes, ensuring their stability. This has led to the application of recently developed control techniques on large-scale systems in the mining processes. One of the most important process of the mining industry is the mineral grinding, as the product particle size impacts, in a significant manner, the recovery rate of the valuable mineral in the separation stages. As a solution, a centralized hybrid model predictive control (HMPC) is presented; this control approach maintains the product particle size on a defined range and minimizes energy consumption, maintaining the grinding plant in a stable operation. As a comparison, a conventional model predictive control with an expert system to handle discrete events was developed, showing HMPC is a suitable solution that can used in the grinding process, with the benefit that it handles in the same controller both discrete and continuous dynamics and events.

Jan 1, 2014

By Trevor Saldanha, Stephen Grano

A key uncertainty in flotation modelling is determining, a priori, the proportion of each mineral which will develop a certain rate constant for different feeds of variable liberation and hydrophobicity. First and foremost is the ability to predict the proportion of minerals that will not be recovered, even at very long flotation times, and which therefore report to the tailing stream as the non-floatable fraction (i.e., having a zero rate constant). Recent empirical evidence has shown there are at least two factors which contribute to heterogeneity in flotation rates and, in particular, the appearance of a non-floatable fraction - heterogeneity in the distribution of adsorbed collector amount on a particle-by-particle basis, even for the same liberated mineral in the same size fraction, and the existence of a critical contact angle below which the bubble-particle union is unstable. In this paper, inferred measures of the critical contact angle for liberated particles are compared with stability model calculations. This has demonstrated that the dependency of the critical contact angle with particle size and mineral specific gravity are explicable by bubble-particle stability considerations. This argument is further extended to the flotation behaviour of composite particles, as a function of liberation class, in which the wetting perimeter of the attached bubble on the composite particle surface is constrained by the presence of a surrounding hydrophilic domain for the case of simple binary composites. Reasons for the different flotation behaviour of composite particles having different textures, as noted in the literature, are also discussed in terms of the stability of the bubble-particle union.

Jan 1, 2014

By F. Bello, R. Yanez, M. Pinto, T. Errazuriz

"Throughout its operation, Minera Esperanza (ME) will deposit one of the largest tonnages rates of high density tailings in the world with a solids concentration of close to 67% by weight. The tailings presently being deposited have a solids concentration of approximately 62% - 64%, and so cannot be used to directly characterize the flow and deposition characteristics of the higher concentration tailings. To increase the knowledge of the behaviour of their tailings, ME, with the support of Golder Associates, developed a large scale tailings deposition test with a capacity of 30,000 tonnes per day (1,200 m3/h). The test was carried out by depositing tailings into two large cells or paddocks in five stages. Multiple spigots were used to allow different flows to be deposited. At each stage, topographical surveys of the natural terrain and the geometry of the deposited tailings, as well as continuous flow measurement and periodical rheological characterization of the discharged tailings were conducted to create a data set against which beach slope models could be calibrated and then used to predict performance of the higher concentration tailings under different deposition scenarios. This study adopted the beach slope prediction model proposed by A.L. Li (Li, 2011). The model was successfully adjusted to the observations made during this large scale field test by applying the values measured in-situ. This paper presents the application of the model, the results obtained, the findings, and the analysis of possible future scenarios. The model was applied, using the discharge flow rate, the geometrical characteristics of the discharge area, and the rheology with its variation along the beach to estimate the development of the beach formation and the steady state of the beach slopes. Through the use of dimensionless variables, the model was applied to higher solids concentration scenarios, obtaining results that would allow beach slope estimation at different deposition stages in multiple scenarios of varying parameters such as flow, rheology and geometry of discharge area."

Jan 1, 2014

By S. Mitra1

"This study aims to investigate coarse particle detachment mechanisms (particle diameter > 150 ?m) utilising both experimental and numerical technique. Two mechanisms were studied – (i) interactions of bubbleparticle (BP) aggregate with vortices and (ii) coalescence of bubble-particle aggregates. On the first mechanism, interaction behaviour of coherent vortex structures with a BP aggregate (bubble diameter db = 3 mm, particle diameter dp = 0.3 mm) was studied using a CFD model in the Reynolds number range of 100 to 1000. Effect of surface hydrophobicity on the BP stability was examined using a range of contact angle boundary conditions. To address the second mechanism, interactions of bubble-particle aggregate (db ~ 4 mm, dp ~ 0.4 mm) with both free gas-liquid interface and individual bubbles were investigated using high speed imaging. Both rebound and coalescence outcomes were observed to be responsible for BP instability leading to particle detachment.INTRODUCTIONIt is widely known that flotation process performs excellent mineral recovery for base metal ore particles that are typically in the range of ~ 20 to 150 µm in diameter (Jameson, 2010). More specifically, higher recoveries are usually reported for particles in the size range of ~20 to 70 µm while outside this spectrum, generally the recovery diminishes significantly. It would be highly desirable to improve the recovery of particles at the coarse end of the flotation size range spectrum which has significant economic benefit (Jameson, 2010). However, it is essential that insights to particle detachment phenomenon, the primary impediment in coarse particle flotation caused by the underlying hydrodynamic factors are first obtained at a greater depth.In an ideal quiescent liquid medium, due to inertia, coarse particles deviate substantially from the fluid streamlines and collision efficiency with bubbles decreases which can only be augmented by increasing turbulence level in the medium sufficiently to make random physical contacts with bubbles. Nonetheless, even if successful contacts are made, it is difficult for these large particles to remain attached to bubbles in a turbulent shear flow environment. There are two major mechanisms postulated for particle detachment – interaction of turbulent flow structures (eddies) with BP aggregate and coalescence among surrounding aggregates. Earlier work of Schulze (1982) theorised a vortex acceleration component to characterise turbulence effect on BP aggregate instability in flotation machines. Wang et al. (2015) investigated bubble detachment behaviour from a stationary particle in a nearly homogeneous and isotropic flow field. Using PIV (particle image velocimetry), it was shown that the local maximum energy dissipation rate for the case of bubble detachment was significantly higher than the no detachment case, and was also higher than the critical value for bubble detachment calculated using Schulze’ theory (Schulze, 1982). Later, Wang et al. (2017) also visualised the BP aggregate instability in a cavity flow leading to particle detachment which was attributed to bubble coalescence, bubble surface oscillation and particle deceleration phenomena."

Jan 1, 2018

By V. A. Masloboev, A. V. Svetlov, D. V. Makarov

"The methods of heap leaching are considered to be the most promising for the low-grade copper-nickel raw materials. The article presents intensification capabilities of the process. Objects of research: the low-grade copper-nickel ores of Moncheplutone deposits (Moroshkovoye Lake, Nyud Terrasa, Nittis-Kumuzh’ya-Travyanaya (NKT), as well as the copper-nickel ore dressing tailings of the “Kola MMC” JSC. The following directions for the intensification of the low-grade copper-nickel raw materials heap leaching have been considered: preliminary electric pulse destruction (EPD) of ore; ore crushing and further sulfuric acid agglomeration. The impact of sulfuric acid concentration (1-3%) on the extraction of non-ferrous metals kinetics from the copper-nickel ore dressing tailings under various conditions of the percolation leaching has been studied. INTRODUCTION The low-grade grade sulfide ores at the abandoned and producing deposits, overburden rocks, mill tailings and non-ferrous slag are thought to be one of the large-scale sources for non-ferrous metals, on the one hand. On the other hand, they are known to be the subjects of emergency environmental danger. For this reason, the use of mine dumps and tailings, as well as the remained ores left in the ground as raw products, and at the same time decreasing the load on environment, are considered to be the pressing ecological and economic issue (Chanturia et al., 2012). Methods of heap hydrometallurgical and bacterial leaching are sure to be potentially productive for processing such low-grade and technogenic raw materials (Petersen, 2016). The early studies of hydrometallurgical method possibility to process copper-nickel ores of the Murmansk region deposits were launched in the seventies of the previous century (Golovko et al., 1978). For referencing purposes, the main types of impregnated ores from the deposits Zhdanovskoye, Kaula, Sopchinsky Plast and Lovnoozerskoye were selected. The metal content varied, as %: 0.46-1.49 of nickel, 0.01-0.62 of copper. In the first experiments, the solution containing 150g/l of H2SO4 and 135g/l of NaCl, was used in the capacity of leaching reagent. The possibility of underground metals leaching from the ores of the Lovnoozerskoye deposit was justified due to the performed laboratory and further large-sized tests."

Jan 1, 2018

By A. Bastrzyk

Text The mining and refining of minerals generates large amounts of solid waste. The waste from cleaning operations constitutes up to 90% of the total production. Although some of them can be used in mining, civil enegineering, construction, agriculture, most of them must be disposed in dumps and slurry ponds, causing major economic and enviromental problems (Alonso, 2002; Alon-so, 1999). The refuse from minerals cleaning may have considerable valuable particles content, which can be used in industry. Thus, the recovery of these particles from minerals waste by using a cleaning method effective at fine particle size, may overcome these consequences. Surfactants are used in numerous applications including emulsification and solid surface modification. In the oil agglomeration of minerals, the ionic surfactants (both anionic and cationic) are used for the hydrophobization of mineral surface and the oil-water emulsion preparation. When the cationic surfactant is injected into the oil-water mixture, surfactant molecules adsorb at the oil-water interface, changing droplets? properties. The addition of anionic surfactant to the mineral suspension was found to modify the solid-liquid interface. In this paper, the condition and mechanism of selective separation of magnesite from quartz are presented. A satisfactory was achieved with the amount of anionic collector (sodium oleate) equal to 15.2 mg/gsolid and with the amount of cationic collector 27.9 mg/gsolid for cetyltrimethylammonium bromide (CTAB) and 16.9 mg/gsolid for dodecyloammonium hydrochloride (DDAHCl) at pH 8. At these conditions, the amount of agglomerated carbonates was about 12% for CTAB and 5% for DDAHCl.

Jan 1, 2014

By X. F. Cao

There was a large reserve of bauxite resources in China. And these resources were mainly the dias-pore-bauxite and contained plenty of aluminosilicate including kaolinite, illite and pyrophyllite. Reducing the contents of aluminosilicate would be significant to the using of Chinese bauxite resources. In this paper, from the single mineral flotation experiments, the surface properties and flotation beha-viours of aluminosilicate including kaolinite, illite and pyrophyllite, using dodecyl amine (DDA), N, N-dimethyl-dodecyl amine (DRN12) and N-dodecyl-1, 3-propane diamine (DN12) as collectors, had been investigated. The flotation results shown that the flotation behaviours of aluminosilicate had been influenced greatly by three amine collectors; and the effect was in the order of DN12>DRN12 >DDA. On the basis of FT-IR spectra and zeta potential measurements, the ionization of surface hydroxyl, as well as isomorphic exchange of surface ions, accounted for the mineral surface charges. And the mechanisms of interactions between the mineral surface and collectors mainly included two modes: electrostatic adsorption and hydrogen bonding; for the DDA and DRN>DDA. 12, the mechanism was mainly electrostatic adsorption; and for the DN12, the mechanisms of electrostatic adsorption and hydrogen bonding both existed. Results of quantum chemistry research shown that the collecting ability of amine collectors was greatly influenced by the electro-negativity of N in the amine molecules; and The |E(EHOMO| and ?E (HOMO-ELUMO) of N atom in DRN12 and DN12 were lower than that of DDA, and the positive charge of ?N group in DRN12 and DA12 were higher than that of DDA. All these calculation results could explain the collecting power of DN12>DRN12>DDA.

Jan 1, 2014