Search Documents

By B. Das

The processing of banded iron ore by direct anionic and reverse cationic flotation to produce pellet grade concentrate is investigated. This low-grade iron ore, known as banded hematite quartzite (BHQ) contains 41.8% Fe, 41.5% SiO2, 1.2% Al2O3, and 0.5% LOI. The flotation behavior of BHQ is studied by varying the effect of concentration of collector, frother, dispersant and pH. Oleic acid and dodecylamine are used as the anionic and cationic collectors respectively. The parameters that gave the best results in cell flotation are utilized in 100 mm diameter flotation column. All the results are compared with regard to the iron grade and recovery in concentrate. It is observed that, anionic collector with dispersant dosage of 220 g/ton, at pH ~8.5 is selective and yielded a high-grade iron concentrate with low silica as impurity. Also, it is possible to achieve an iron concentrate with 64% Fe at 30-37% weight recovery. The characterization studies of the BHQ ore using X-ray diffraction (XRD) technique and liberation analysis with QEMSCAN® are carried out. The sample contains 58.8% hematite and 37.7% quartz and the liberation of hematite particles are found to be 90.3% in -25 µm size. An alternative statistical modeling approach called response surface methodology was also undertaken to optimize the operating parameters in order to maximize the iron grade and recovery. The predicted results by the model are in agreement with the experimental values.

Sep 1, 2012

By X. Q. Ma

The beneficiation test on low grade phosphate ore from a state of Russia is carried out. The rougher-cleaner ? re-cleaner system is used in the flotation process, The fineness of grind is 39.07% minus 200 mesh. The result indicates that concentrate containing 31.25% P2O5 can be obtained from the flotation feed assaying 6.18% P2O5, with 93.54% P2O5 recovery. The test result is also a guideline for further development of some currently operated phosphate beneficiation plants.

Jan 1, 2014

By V. A. Ivanova

Modification of hydrophobic part of carboxylic collector molecule is an upcoming trend for producing new reagents and changing its flotation properties such as activity, selectivity, sensitivity to hardness salts that inevitably present in the pulp liquid phase in the processing of ores containing calcium minerals. A wide range of apatite collectors ? monoalkyl ethers and monoalkylamides of dicarboxylic acids ? succinic, o-phthalic and maleinic acids have been synthesized by the addition of aliphatic alcohols and amines with various hydrocarbon radical value (from ?11 to ?16) to anhydride of the corresponding acid. Using computer modeling based on ChemBio 3D program of specialized complex Chem?ffice the calculation was carried out of charge distribution on atoms, energy parameters of molecules for investigated compounds. Calculated values of absolute hardness (?=6.75 ? 12.36) and absolute electronegativity (?= 5.67 ? 8.90) of the reagents showed that monoderivatives of dicarboxylic acids refer to the ?hard? type of bases. The degree of a charge transfer during calcium compounds formation of considered collecting agents (?N=0.009 ? 0.143) has been computed. Dissociations, micelle formation in solutions of these reagents and its hydrophobic and collecting properties were investigated in respect to apatite. Dependence of bulk, surface and collector properties on collector molecule architecture (double bond or benzene ring and non-ionogenic functional group in the structure of hydrocarbon radical) has been established. It is shown that experimentally determined dissociation constants (??a=5.16 ? 5.60 for succinic acid derivatives and ??a=3.32-3.78 for maleinic and o-phthalic acid derivatives) perfectly correspond to acidic properties predicted by computer calculations. Compounds of monoalkylderivative dicarboxilic acid have been determined optimum in composition and structure. The results of apatite flotation from apatite-nepheline ores of the Khibiny deposit (the Kola Peninsula) are presented here and show benefits of selected reagents. Keywords: monoalkylderivatives, dicarboxylic acids, reagents, microflotation

Sep 1, 2012

By Steven Bradshaw, Edson Charikinya

The application of high power microwave energy to secondary crusher products has been shown to induce micro fractures and cracks in the ore. This suggests that heap leaching could benefit from microwave-induced fractures, as the extent and kinetics of heap leaching processes depend on the accessibility of grains to lixiviants, which can potentially be improved through microwave treatment. The density and pattern of microwave induced cracks and how these cracks subsequently affect heap leaching recovery has not yet been investigated. The objective of this study was to apply X-ray micro computed tomography (X-ray CT) to investigate microwave induced cracks in large cone and HPGR crushed sphalerite particles within 3D space. The ore particles were microwave treated in a single mode microwave applicator coupled to a switched mode power supply and a water cooled microwave transmission sub system operating at 2.45 GHz. The ore particles were treated at specific absorbed microwave heating energies of between 2 and 3kWh/t by treating at 6 kW of forward power for treatment times of 1 s. X-ray tomography analysis was conducted on fine (-5+4.75) mm, medium (-16+9.5) mm, and large (-25+19) mm sphalerite particles before and after microwave treatment at voxel resolutions of 5 µm, 15 µm and 25 µm respectively. Image segmentation, thresholding and spatial registration techniques were used to study crack patterns in 3D images of HPGR and cone crushed particles. Analysis of the X-ray CT images after microwave treatment shows considerable micro crack formation within the Cone and HPGR crushed particles. The cracks pattern showed interphase cracks propagating across all phases, with no evidence of preferential cracking. A greater density of microwave induced cracks was observed on fine (-5+4.75) mm particles compared to the medium (-16+9.5) mm and (-25+19) mm large particles. The results showed overall increased particle porosity following microwave treatment.

Jan 1, 2014

By Xiaoping Xu

An albitization granite type tantalum-niobium ore from Jiangxi Province, China was taken as the research object in this paper. The main valuable minerals in this ore are tantalite-columbite and uranmicrolite, and the minerals that can be comprehensively recovered include cassiterite, sulfide minerals, topaz, zinnwaldite, and quartz-feldspar. Based on the research results of process mineralogy, the roughing process of gravity separation for coarse particles combined with flotation for fine particles is proposed. The combined cleaning process of flotation-gravity-magnetic-electric-hydrometallurgical separation is adopted for the rough concentrate of gravity separation while the combined cleaning process of gravity-flotation- hydrometallurgical separation is adopted for the rough concentrate of flotation. High intensity magnetic separation is used to separate and recover zinnwaldite and quartz-feldspar from gravity tailings. By mineral processing for the crude ore containing (TaNb)cassiterite concentrate is 0.0003% with a grade of Sn 63.22% and a recovery of Sn 47.42% while the yield of sulfide concentrate is 0.0783% with a grade of Pb 33.15% and Zn 27.09% which can be separated to get lead and zinc concentrate respectively. The yield of topaz concentrate is 0.1545% and the topaz mainly distributed in the size range of -0.4+0.074mm, which can be made into abrasive products of different particle sizes after classification. The yield of zinnwaldite concentrate is 16.91% with a grade of Liwhiteness of 75%, which is a glass-ceramic material of good quality. 2O5 0.0346%, Sn 0.04%, Pb 0.10% and Zn 0.33%, the tantalum-niobium concentrate with a yield of 0.00278%,a grade of (TaNb)2O5 53.61% and a recovery of (TaNb)2O5 44.49% is obtained. And the yield of 2O 1.34% and Rb2O 0.40%. The yield of quartz-feldspar concentrate is 30.42% with a grade of K2O+Na2O 8.98% and Fe2O3 0.11% and a natural All of tantalum, niobium, cassiterite, topaz, zinnwaldite, quartz, and feldspar are recovered effectively. Keywords: tantalum-niobium ore, gravity separation for coarse particles, flotation for fine particles, comprehensive recovery

Sep 1, 2012

By Sarra Scherbakova, Alexander Kurkov, Andrey Egorov

"Deep concentration of iron ores involves extraction, in addition to magnetite concentrate, of hematite and martite concentrates and recovery of other valuable components. A flotation technology was designed specifically for finely disseminated hematite ore, allowing producing saleable hematite concentrate containing 64-66% Fe. The main process challenge is caused by the presence of other ferruginous minerals such as carbonates, silicates, and phosphates, and fine hematite and martite mostly concentrated in the -0.044 mm fraction. Main operations of the processing circuit are removal of slime, flotation to remove impurities (carbonates, phosphates etc.) with an anionic phosphorous collector in an alkaline environment, hematite and martite flotation using same collector in a slightly acidic environment to produce commercial iron concentrate. Tailings of wet magnetic separation of magnetite containing 24.5% Fe and finely disseminated hematite ore containing 51% Fe were processed to produce iron concentrates with a yield of 15% and 50%, respectively, containing approximately 65% Fe and 5% of silica. Hematite flotation tailings had the highest content of gold (up to 0.09 - 0.11 g/t), while in other products it never exceeded 0.02 g/t. Using a Knelson concentrator was able to recover 40 to 45% of the gold into 3.31 g/t Au gravity concentrate. The success of gravity concentration is due to high gravitational contrast of gold to mostly quartz and aluminosilicates in the hematite flotation tailings. In general, the proposed process can be used as a solution to the challenge of selective concentration of finely disseminated iron minerals."

Jan 1, 2014

By U. Dmitrakova, G. Sedelnikova, D. Kim, E. Savari

"The paper presents the results of research on the development of gold and silver extraction technology from refractory gold sulphide flotation concentrate of one deposits of Nord-East of Russia. The concentrate is due to the complex mineral composition. Gold and silver are finely disseminated in sulphide minerals (arsenopyrite and pyrite partially oxidized by 7-11%). These are characterized by high content of silver 219 g/t and sulphide sulfur 32%, the presence of poorly soluble silver minerals (silver sulfosalts, fahlore, finely dispersed hypergenic acanthite in iron hydroxides and jarosite, etc.), and impurity minerals capable of interacting with cyanide (pyrrhotite, marcasite, nonferrous sulphides) and causing higher than normal cyanide consumption. Pretreatment of refractory sulphide concentrate by biooxidation using a mixed association of mesophilic and moderately thermophilic bacteria at a temperature of 36-40 °C for 120 hours oxidized arsenopyrite by 97.5%, pyrite by 93.5%, unlocked refractory gold, and generally oxidized the minerals absorbing cyanide and oxygen before cyanidation. Further oxidation of these minerals-absorbents was facilitated by the aeration in calcareous medium of the solid biooxidation residues of the concentrate. Sorption cyanidation of the solid biooxidation residues with addition of lead (II) of recovered 91.2% of gold and 82.9% silver from biooxidation residue, compared with 80.1% and 46.6%, respectively, for sorption cyanidation without the preceding biooxidation step. Biooxidation of the concentrate prior to cyanidation improves the recovery of precious metals, especially silver, and significantly reduces cyanide consumption from 18.7 kg/t to 3-5 kg/t of concentrate. INTRODUCTION Biooxidation of gold sulphide concentrates using acidophilic microorganisms has been successfully applied worldwide (van Aswegen et al., 2007; Gericke et al., 2009; Sovmen et al., 2007; Sovmen et al., 2009). At least 15 full-scale plants for tank biooxidation of sulphide concentrates are presently in operation, and the construction of new ones is planned (Bulaev et al, 2015)."

Jan 1, 2018

By P. Braga, A. Chaves, S. França, A. Luz

"In Brazil, there are no official reserves of molybdenum, and the unofficial reserves are modest. Therefore, the molybdenum ore (molybdenite) produced as a co-product or by-product of emerald mining in the region of Campo Formoso, BA, has arisen as the only economic option. The flotation process is commonly used in Brazil for the recovery of molybdenite from emerald mining tailings, but it produces low-content molybdenite concentrates, thereby resulting in a product with low economic value. The molybdenite concentrate produced in Campo Formoso contains 83.5% MoS2 (50% Mo), which is less than the international standard product that contains > 90% MoS2 (54% Mo).This low value is due to the presence of talc, which is a naturally hydrophobic mineral that is also floated with the molybdenite during the flotation process. Separability studies were done in a Partridge-Smith cell using dextrin and quebracho as a molybdenite depressor in solution at different concentrations and pH values to produce a technical-grade concentrate (i.e., 90% MoS2). These basic studies were accompanied by measurements of the zeta potential and contact angle, which was determined by the capillary rise method. The results of these floatability studies were used in bench flotation tests, which were performed in a Denver laboratory flotation cell. A molybdenite concentrate of 93.4% MoS2 was obtained when dextrin was used at a concentration of 100 g/t."

Jan 1, 2014

During incineration of municipal solid waste (MSW), some heavy metals and other environmentally harmful elements are liberated into bottom ash. The stricter environmental regulations require a higher immobilization efficiency of the ash before its safe disposal and application. Vitrification is one of the promising options, and has the advantages of high destruction efficiency of organics, high immobilization of heavy metals, and large volume reduction. The main components of the vitrified slag are SiO2, CaO, Al2O3, Fe2O3, Na2O and MgO, and the compositions have direct effect on the glass formation during vitrification, and further on the physical and mechanical properties of the slag. To provide essential data for the utilization of bottom ash as vitrified slag, the phase relations and thermodynamic properties of the oxide system need to be systematically investigated. In the present study, the liquidus temperature of the typical vitrified bottom ash slag was determined by using differential scanning calorimetry (DSC) measurement. High temperature equilibrium experiments were conducted to investigate the phase relations of the sub oxide system of CaO-SiO2-Na2O by means of Scanning Electron Microscopy (SEM), Electron Microprobe Analysis (EMPA) and X-ray Diffraction (XRD). The results show that the melting temperature of the vitrified bottom ash is around 930°C. In the CaO-SiO2-Na2O system with less than 50 mol% SiO2, the liquidus temperature de-creases with increasing amounts of Na2O along the tie-line of Na2O-Ca3Si2O7. Two compounds Na2Ca3Si2O8 and Na4Ca8Si5O20 are identified in the oxide system.

Jan 1, 2014

The addition of copper sulfate to mineral slurries in order to ?activate? sulfide mineral surfaces for enhanced collector molecule adsorption, and hence enhanced recovery via flotation, is a com-mon mineral processing practice. It has been established in a laboratory situation that the addition of CuSO4 in conjunction with xanthate collector increases the flotation rate of pentlandite as compared to the addition of collector alone. However, it remains unclear whether the addition of CuSO4has a similar effect within mineral processing circuits. We examine here the effect of pre-activation oxidation on the copper activation of pentlandite and monoclinic and hexagonal pyrrhotite. All activation experiments were carried out at pH 9 using a total solution content of copper ions equivalent to one monolayer (0.210 -4 moles, 110-4M). Copper loss from solution was extremely rapid in all cases with less than 10 % remaining after 10s. EDTA extraction and solution analysis clearly demonstrated that copper activation was via direct surface adsorption and not an ion exchange process, as is the case for sphalerite, and that most copper on the surfaces is in the form of Cu(I). ToF-SIMS analyses of the mineral surfaces subsequent to copper activation show increased surface oxidation on increased conditioning time prior to copper activation. However, there is a significant decrease in surface oxidation on comparison of samples that have otherwise been prepared in the same manner but where one has been exposed to copper solution rather than water. This suggests that copper activation stabilises the surface and reduces the propensity for oxidation. Regardless of the length of pre-activation oxidation time only Fe(III) (no Fe(II)-S) was observed by XPS analysis, indicating a highly oxidised surface layer dominated by Fe-O-OH species. The presence of Cu(II) on the mineral surface is indicative of the formation of Cu(II)-containing precipitates and indicates non-mineral specific activation resulting in increased recovery but lower grade. Mineral specific copper adsorption, as evidenced by the presence of Cu(I), is required to improve both grade and recovery. Prolonged oxidation prior to copper activation causes a reduction in the Cu(I) to Cu(II) ratio on the mineral surfaces as compared to either fresh surfaces or surfaces oxidised for 1 minute only. This strongly indicates that the copper activation process is less effective on highly oxidised surfaces.

Jan 1, 2014

By J. K. Qu

As one of the key inorganic chemical industries, the chromate chemical industry has spawned extensively public concerns due to the resulted environmental pollution. The cleaner production technology for chromium compounds bases on sub-molten salt medium developed by the Institute of Process Engineering, Chinese Academy of Sciences has greatly decreased the reaction temperature and energy consumption, significantly in-creased the utilization ratio of the chromium element, and successfully achieved the comprehensive utilization of chromite resources and zero emission of chromium-containing residue. The separation process of production is the most important components in the cleaner technology. In this work, we studied two parts: the first is the removal of SiO2, Al3+ from the system and the recycling utilization of alkali metal medium through adding Ca(OH)2 and CaO; the second is to get more pure K2CrO4 crystalloid and remove K2CO3 from KOH solution through evaporation to prepare raw material for manufacturing Cr2O3 and get 50%(wt) KOH. The results obtained show that Ca(OH)2 can remove Al3+ more than CaO and has lower caustic ratio than CaO when they were added 110% of theoretic quantity. The optimal pure K2CrO4(96%) can be gained at 45 Celsius degree in 30% KOH solution and K2CO3 in 50% KOH solution could be decreased to 3.5%(wt) at 40 Celsius degree. And then K2CO3 can be causticized with adding Ca(OH)2 to recycle potassium alkali. The impure material can be re-moved and suitable raw material for manufacturing Cr2O3 can be gotten and reaction medium can be also recycled in this process technology, realizing cleaner production effectively.

Jan 1, 2014

By Gülay Bulut, Mustafa Özer, Yunus Emre Benkli, Olgaç Kangal, Istanbul Technical University, Mustafa Tarkan

"Zeolites are naturally occurring as hydrated aluminosilicate minerals. They belong to the class of minerals known as “tectosilicates” and are related to the common minerals feldspar and quartz. Seven natural zeolites that occur in large, commercially exploitable deposits, are: clinoptilolite, chabazite, mordenite, phillipsite, erionite, analcite, and ferrierite. Among them, clinoptilolite is the most abundant one and is not the best known, but is one of the more useful natural zeolite. Clinoptilolite [(Na3K3) (Al6Si30O72) 24 H2O] is very closely related to heulandite and is currently being considered for disuse it self as it may just be a variety of heulandite. It differs from heulandite significantly only in its enrichment in potassium and slightly more silica and it is argued that a separate mineral is not needed.There are large zeolite deposits in western part of Turkey. The sample used in this study was taken from the Gördes region of these deposits. Screen, chemical, XRD and mineralogical analyses were used to determine properties of the natural zeolite sample used in this work.According to the size distribution of the sample, it is found that the zeolite sample used in this study is below 1 mm in size and almost 80% of it is below 0.5 mm. X-Ray Diffraction (XRD) and mineralogical analyses show that the natural zeolite is found to be in the forms of clinoptilolite and heulandite. Clinoptilolite forms as a devitrification product of volcanic glass in tuffs. Quartz, clay minerals, orthoclase, plagioclase, biotite, seruzite-muskovite and epidote were observed as impurities. XRD analysis also shows that the sample contains approximately 58-60% clinoptilolite, 5% quartz, 5% feldspar, 10% smectite, 5- 10% illite and mica and remaining volcanic tuffs. Several types of mineral processing methods were performed in order to remove impurities from the natural zeolite sample to produce high purity zeolite. Gravity separation methods such as shaking table and superpanner were carried out for separating heavy minerals, while high intensity dry magnetic separation was used for discarding magnetic minerals."

Jan 1, 2003

By S. M. Narbekova, L. V. Semushkina, Zh. A. Aldybayeva, A. A. Mukhanova, D. K. Turysbekov, N. K. Tussupbayev

More complex and heavy-concentrating oxidized and mixed sulphidic oxidized ores are involved in production because of increasing needs for non-ferrous metals. Extraction of the oxidized minerals of non-ferrous metals general in current technologies. The problem is solved to oxidized polymetallic ores the preliminary selective sulphidization is the oxidized surface of the components by means of hydrogen sulphide, sulphide and calcium polysulphide, and also element sulphur, etc. The task was to study details of flotation of the oxidized lead-bearing ore of the Zarechnoe deposit (Kazakhstan) with calcium polysulphide as sulphidation. According to chemical analysis initial samples of the ore contain, %: lead – 4.8; zinc – 0.1; general iron – 0.81. Phase structure lead is characterized by the oxidized form of 57.76-64.5 %; by sulphidic status of 25.5-32.64 %, and by plyumboyarosite of 19.0-23.02 %. Researches on flotation beneficiation of oxidized lead-bearing ore are conducted. Sulfidizator gave to grinding, on flotations there were used the collector (butyl xanthogenate of sodium) and frother (T-80). Experiments were conducted with a new sulphidizator – calcium polysulphide. The latter is obtained by interaction of CaO calcium oxide with sulfur and water at high temperature with component mass the following ratio S:CaO:H2O =10:5:85. Extent of mill initial ore was optimised (88.42 % of - 0.071 mm grade). For the optimum mill mode the studies on matching of an optimized consumption of sulphidizators are performed. On basic technology with application of sulphide of sodium as a sulphidizator at optimum mill, the lead concentrate with the content of lead 64.4 % at extraction of 86.6 % was received. The content of cerussite in a concentrate was about 14.9 % at extraction of 82.1 %. With application of calcium polysulphide as a sulphidizator the lead concentrate with the content of lead 68.0 % at extraction of 88.0 % was received. The content of cerussite has made 16.0 % at extraction of 85.0 %. Application of a new sulphidizator allows to increase extraction of lead in a concentrate from 64.4% to 68% and cerussite extraction – from 82.1 % to 85.0 %. The possibility of application of calcium polysulphide as a sulphidizator instead of conventional sulphurous sodium was established.

Jan 1, 2018

By A. V. Yevdokimov, Ye. V. Bogorodsky

The paper presents the results of the research on the development of gravity concentrates processing technology (gold grade is from 50 g/t to 1 kg/t and over) using intensive cyanidation with gold recovery to pregnant solutions followed by precipitation of metals from them using various methods. Test work and pilot plant results confirm that a new developed hydrodynamic regime provides an efficient treatment of gravity concentrates of polydisperse composition without their grinding and preliminary desliming. The resulting pregnant and washing solutions are amenable to metals recovery using electrowinning, cementation onto zinc dust and CIS. Cone plants with a lower ball valve for cyanidation of unground gravity concentrates developed by IRGIREDMET JSC have been successfully tested at a number of Russian operations. Currently, a modular plant equipped with gold electric precipitation from pregnant solution unit is successfully operated at a Russian gold processing plant. Cyanidation of the resulting high-grade gravity concentrate is carried out at the concentration of 8-10 g/L NaCN and 10 g/L NaOH. Gold recovery to the solution is 97-98%. Electrowinning is carried out in flow cell GNC-40M. In this case, the residual gold concentration yield is 0.3-0.5 mg/L. Also, a modular plant for relatively low-grade middlings (50-100 g/t Au) of gravity concentration has been introduced. The concentration of NaCN and NaOH is 2-3 g/L and 1.5-2 g/L, respectively, during leaching. This plant is equipped with a unit for gold cementation from pregnant solution with zinc dust. This cementation unit is of original design. It is made in the form of a filtering device and is composed of several layers of carbon fiber which contacts with zinc powder. The residual gold concentration yield from a cementation unit is less than 0.1 mg/L. Gold recovery is 93-97%. In 2017-2018, the introduction of intensive cyanidation modular plants to gravity concentrates will be planned at new projects of Russia and the CIS.

Jan 1, 2018

By W. G. Liu

Phenyl malonic acid (PMA), a new chelating collector, which contains a phenyl structure and a malonic acid chelating group, has been synthesized and its collecting capabilities to calamine, hematite, quartz and hemimorphite are also studied in laboratory. From the experimental results, it can be seen that the PMA has somewhat flotation ability to calamine, hematite and quartz, while it nearly has no collecting ability to hemimorphite. With the increase of PMA concentration, the flotation recovery of calamine increases. When the dosage of PMA was 560g/t and at pH=7~9, the flotation recovery of calamine gets its maximum of 45.94%. The test results about the influence of pH on the flotation recovery of quartz show that the flotation recovery increases with the increase of pH, and the maximal flotation recovery can be gained in alkaline media. On the other hand, PMA has stronger flotation capability to hematite than to other minerals. The flotation recovery of minerals increases with increase of PMA concentration. When the dosage of PMA is 560g/t and at pH=5~7, the flotation recovery of hematite is 82.96%. Mean-while, the influence of pH on the flotation recovery of hematite was studied and test results showed that, as pH increases, the flotation recovery sharply rises until pH=4, then the increasing rate de-creases outstandingly, at pH=6 the flotation recovery reaches its maximum of 82.96% and it de-creases speedily in alkaline media. Finally, through the measurement of infrared spectroscopy and in terms of solution chemistry of collector, the flotation mechanism has been discussed. It was concluded that the adsorption of PMA on minerals surface is chemical adsorption in nature through two oxygen atoms in the polar group of phenyl malonic acid chelating with the metal ions of minerals surface to form a hexagon-cycle chelate complex: C(=O)-O-M-O-(O=)C.

Jan 1, 2014

By N. D. Dementieva

Based on lab and pilot-plant tests to recover gold, silver and lead of a Russian deposit, a collective and flotation concentration flow sheet with lead and sulfide concentrates was proposed. The type of the deposit is gold-sulfide-quartz-bearing. The recovery of gold, silver, and lead to a lead concentrate was 47.4%, 68.1% and 70.7%, respectively. The grade of gold and silver grade was 170 g/t and 372 g/t, respectively. The mass percent of lead, zinc and arsenic mass percent was 41.7%, 0.34% and 0.63%, respectively. The recovery of gold and silver recovery to a sulfide concentrate was 50.1% and 28.8% at the grade of gold 20.5 g/t and silver 66.2 g/t. Sulfide concentrate with arsenic mass percent ~3% was biooxidised followed by CIL and obtaining metal at the site as well as zinc concentrate from bioleaching solutions with zinc mass percent 45% at its 64% recovery. The total gold and silver recovery using a developed technology with the account of their treatment at a polymetallic plant was 92.2% and 93.7%, respectively.

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 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 Y. E. Brylyakov, M. A. Kostrova

"The apatite staffelite ores (ASO) of Kovdor deposit are dominated by fine-grained aggregates containing both phosphate minerals and silicates — vermiculite, smectites, zeolites. These minerals exhibit ion-exchange properties. In this connection, the magnitude of cation exchange, along with the content of P2O5 and CO2, is an important property of apatite staffelite ore, which largely determines the performance of concentration processes. In the examined ASO samples, the magnitude of cation exchange measured in terms of Ca2+ is 2546-4790 g/ton. The conducted laboratory studies of apatite staffelite ores with various mineral composition showed that adding calcined soda improves the recovery of P2O5 into the flotation concentrate. Full-scale tests were conducted at the apatite staffelite ore processing plant at Kovdor Mining and Concentration Operation and demonstrated the high performance of the proposed agent treatment. The test results showed that in the flotation of apatite staffelite ores, the optimum calcined soda feed rates range from 3,500 to 5,000 g/ton of the flotation feed. With close flotation feed and concentrate grade parameters, the P2O5 recovery gain is 17%. The effect of adding soda is associated with the desorption of the hardness cations from the minerals, precipitation in the pulp and, accordingly, improvement in the ionic composition of the liquid phase of the flotation feed due to a reduced content of calcium ions. Based on the test results, the proposed agent treatment with an elevated feed rate of calcined soda was implemented at Kovdor Mining and Concentration Operation in the flotation of apatite staffelite ore. The apatite staffelite ores (ASO) of Kovdor deposit are dominated by fine-grained aggregates containing both phosphate minerals and silicates — vermiculite, smectites, zeolites. These minerals exhibit ion-exchange properties. These minerals have certain properties requiring a more detailed examination for a better understanding of the flotation properties of apatite staffelite ores."

Jan 1, 2018

By Rodney J. Hundermark, Sharif Jahanshahi, Shouyi Sun

"The major platinum producers in South Africa make use of electric furnaces for the melting of platinum group metal (PGM) bearing nickel – copper concentrates. To gain better understanding of the furnace operation, research was conducted at CSIRO Minerals in Melbourne, Australia. One aspect of the research project was the investigation of the factors affecting the electrical conductivity of melter type slags.Electrical conduction in slags can occur through two mechanisms: ionic and electronic. There is good understanding of the ionic mechanism. In slags containing high levels of iron, the dominant mechanism is electronic as a result of charge hopping (electrons or holes) between ferric and ferrous ions. There is limited understanding of the electronic mechanism and one of the aims of the research was to investigate this mechanism further.Experimental work was carried out at 1450 °C on Al2O3–CaO–FeOx–MgO–SiO2 slags similar in composition to the melter slags (typical composition range (wt%): Al2O3: 5, CaO: 5-15, FeOx: 10-30, MgO: 15-25, SiO2: 40-60). The approach was to vary the oxidation state of three different basicity slags and measure the conductivity response. The slags had molar (CaO+MgO)/(Al2O3+SiO2) ratios of 0.43, 0.64 and 0.94 and FeOx contents of up to 40wt%. A twoelectrode technique was employed with a shallow layer of slag contained in a magnesia crucible. The small amount of slag facilitated relatively quick equilibration (up to one hour) with the gas atmosphere. Experiments were typically started in air and sequentially reduced using different ratios of CO and CO2 gases.Conductivity increased with increasing basicity and increased significantly with iron oxide content. Above 20wt% FeOx, electronic conduction was significant and the conductivity varied with the oxidation state of the slag. The typical response of the conductivity to the change in oxidation state was the following: starting in air, as the slags became more reduced, the electrical conductivity increased to a maximum at around pO2 = 10-7 to 10-4 atm and then decreased with further reduction. The value of the pO2 at which the maximum occurred was dependent on the total iron oxide content and basicity of the slag. The magnitude of the conductivity of the slags increased with increasing FeOx content in a range of 20 to 170 S/m for 20 to 40wt% FeOx. For a given FeOx content in the slags, the oxidation state dependence of the conductivity varied with slag basicity. The trend observed was that the maximum in the conductivity occurred at higher oxygen partial pressures for the lower basicity slags."

Jan 1, 2003