The release of phosphorus(P)from anaerobic sediments becomes the dominant source of P loading with effective control of external P pollution.As a crucial component responsible for binding P,vivianite(Fe_(3)(PO_(4))_(2...The release of phosphorus(P)from anaerobic sediments becomes the dominant source of P loading with effective control of external P pollution.As a crucial component responsible for binding P,vivianite(Fe_(3)(PO_(4))_(2)·8H_(2)O)in sediment inevitably impacts the P level and transformation.The release of P from vivianite mediated by sulphide was investigated using simulated overlying watersediment and chemical reaction systems.The percentage of redox-stable P in the sediments increased with vivianite input in the overlying watersediment system.Increasing P concentrations in both the overlying water and interstitial water occurred before day 10,accompanied by a decreasing percentage of redox-sensitive P in the sediments driven by sulphide.The continuous release of P from vivianite clarifies the influence of sulphide on promoting vivianite dissolution in a chemical reaction system with vivianite and sulphide solution.Additionally,Mössbauer spectrum and nanoscale secondary ionmass spectrometry(NanoSIMS)images based on the chemical reaction with^(57)Fe isotope labelling demonstrated the presence of initial vivianite,newly produced vivianite,and FeS_(2).展开更多
The leaching behavior of main metallic sulphides in zinc concentrate under atmospheric oxygen-rich direct leaching conditions was studied through mineralogical analysis. The results show that the sulphides dissolve ob...The leaching behavior of main metallic sulphides in zinc concentrate under atmospheric oxygen-rich direct leaching conditions was studied through mineralogical analysis. The results show that the sulphides dissolve obviously except pyrite. Based on the relationship between elemental sulfur and the residual sulphides in the leaching residue, the dissolution of sphalerite, chalcopyrite, covellite and galena is assumed to follow the indirect oxidation reactions, where the acidic dissolution takes place firstly and then the released H2S transfers from the mineral surface into bulk solution and is further oxidized into elemental sulfur. The interface chemical reaction is further supposed as the controlling step in the leaching of these sulphides. The direct electrochemical oxidation reactions are assumed to contribute to the dissolution of pyrrhotite, which is controlled by the diffusion through elemental sulfur layer.展开更多
The relationships between the sulphide capacity index and the optical basicity, the mole fraction of oxygen ion and the Bell's ratio were investigated based on extensive lab scale equilibrium and industry scale qu...The relationships between the sulphide capacity index and the optical basicity, the mole fraction of oxygen ion and the Bell's ratio were investigated based on extensive lab scale equilibrium and industry scale quasi-equilibrium experimental data in the temperature range of 1300 1600℃. Although the sulphide capacity index has good relations with different representations of slag basicity. according to the data obtained under the lab scale equilibrium experimental conditions,the similar relations do not exist according to the data obtained under the industry scale quasi-equilibrium experimental conditions. So it is concluded that the sulphide capacity index, which has been considered as a measure of the slag basicity. can not be used for virtually all oxide slags of interest in the field of ironmaking and steelmaking.展开更多
The facile chemical synthesis of silver sulphide nanocrystals from metal-loaded organic media, containing a silver-selective organophosphorous ligand as extractant, is reported. The method involves the phase-transfer ...The facile chemical synthesis of silver sulphide nanocrystals from metal-loaded organic media, containing a silver-selective organophosphorous ligand as extractant, is reported. The method involves the phase-transfer of silver species from aqueous nitrate media to organic solution using the commercial extractant Cyanex? 471x (tri-isobutylphosphine sulphide, Cytec Co.) as extractant, followed by precipitation stripping using ammonium sulphide as strip reagent. The nanoparticles were structurally characterized, and some aspects of the synthetical process, are briefly discussed. Under the conditions studied, the extractant Cyanex? 471x was able to act as stabilizer adsorbing on the particles surface, maintaining the size of the particles nanometrical.展开更多
A logic fault tree of mine spontaneous combustion of sulphide ores was built by the fault tree analysis (FTA) based on a lot of mechanism investigation of sulphide ore spontaneous combustion in more than ten mines an...A logic fault tree of mine spontaneous combustion of sulphide ores was built by the fault tree analysis (FTA) based on a lot of mechanism investigation of sulphide ore spontaneous combustion in more than ten mines and review of a great amount of relevant展开更多
In our study we investigated a refractory copper-nickel sulfide ore separation by using a cyclonic-static micro-bubble flotation column (FCSMC). The process mineralogy of the main products was studied. Using a scannin...In our study we investigated a refractory copper-nickel sulfide ore separation by using a cyclonic-static micro-bubble flotation column (FCSMC). The process mineralogy of the main products was studied. Using a scanning electron microscope-energy dispersive system (SEM-EDS) and an X-ray spectrometer the mineral category and content of samples were analyzed. By using a mineral liberation analyzer (MLA) the mineral liberation characteristics were revealed. It is shown that in roughing feed the monomers liberation degree of nickel pyrite and chalcopyrite take up 84.11% and 88.82%, respectively. In tailings, the lost nickel pyrite and chalcopyrite are mainly monomers. Therefore, strengthening the micro-fine particle recovery capacity is the key to increase recovery.展开更多
The Devonian volcano-passive continental margin in southern Altay is a significant volcanogenic massive sulphide metallogenic belt. Acidic volcanism has been dominant on the inner side of the volcano-passive continent...The Devonian volcano-passive continental margin in southern Altay is a significant volcanogenic massive sulphide metallogenic belt. Acidic volcanism has been dominant on the inner side of the volcano-passive continental margin, i.e., near the old land, resulting in a Pb-Zn metallogenic sub-belt, in which the ore deposits are hosted by sedimentary rocks in volcanic series, as represented by the large Koktal Pb-Zn deposits. In the central part of the margin far away from the old land, bimodal volcanic formations are well developed, forming volcanics-hosted Cu-Zn metallogenic sub-belts, e.g., the large-scale Ashele Cu-Zn deposit. The Qiaoxiahala sub-belt on the outer side of the margin near the ocean ridge is located at the spreading central trough, where ophiolite suites are developed. This type of deposits is rich in gold and copper, similar to the Cyprus-type Fe-Cu-Au metallogenic sub-belt in metallogenic environment (represented by the Qiaoxiahala medium-scale Fe-Cu-Au deposit). From the old land to the ocean, the mineralizing age becomes younger, i.e., from Early Devonian→Early and Middle Devonian→Middle Devonian, forming a complete metallogenic zoning series on the volcano-passive continental margin. Comparative studies show that the massive sulphide deposits distributed on the volcano-passive continental margin are different from those formed under a plate subduction regime and oceanic ridge environment; the former have their unique features and wide distributions, representing a new type of volcanogenic massive sulphide deposits—the Altay type.展开更多
Mechanochemical sulfidization of a mixed sulfide/oxide copper ore by co-grinding with sulfur and additives including Mg(NO3)2 and Fe(NO3)3 salts and iron,aluminum and magnesium powders was investigated for the first t...Mechanochemical sulfidization of a mixed sulfide/oxide copper ore by co-grinding with sulfur and additives including Mg(NO3)2 and Fe(NO3)3 salts and iron,aluminum and magnesium powders was investigated for the first time.Also,the influence of sulfidization during the wet-milling process was examined on the separation efficiency and recovery of copper in detail.The results demonstrated that co-grinding with sulfur solely had the best flotation performance at the value of 0.5 wt.%and it was attributed to the possible existence of S\\O bonding on copper oxides surfaces.In addition,adding magnesium nitrate salt,magnesium powder,iron nitrate salt and aluminum powder as additive associated with 0.5 wt%sulfur into ball milling caused the flotation improvement at the amounts of 0.2 wt%,0.2 wt%,0.5 wt%and 0.5 wt%,respectively.Also,the effect of grinding time and sulfidization pH with 0.5 wt%sulfur solely was determined and pH s of 7.5 to 8.5 gave the best results.The highest recovery(75.76%)and separation efficiency(63.44%)were achieved at pH of 7.5 and 8.5,respectively.展开更多
Microwave assisted leaching of complex copper sulphide concentrate with ferric chloride was investigated, and its mechanism was analyzed. The results show that the leaching rate by microwave irradiation heating is mu...Microwave assisted leaching of complex copper sulphide concentrate with ferric chloride was investigated, and its mechanism was analyzed. The results show that the leaching rate by microwave irradiation heating is much faster than that by conventional heating.展开更多
Flotation reagents have a complex behaviour in the beneficiation of base minerals in clayey ores.Interaction effects of reagents on the efficiency of copper flotation for a highly clayey low-grade sulphide ore were in...Flotation reagents have a complex behaviour in the beneficiation of base minerals in clayey ores.Interaction effects of reagents on the efficiency of copper flotation for a highly clayey low-grade sulphide ore were investigated using a central composite design.Preliminary results showed that sodium-isopropyl-xanthate(SIPX)and O-isopropyl-N-ethyl-thionocarbamate(IPETC)were found to be the most efficient collectors in the presence of lime as the pH regulator.The effects of dosage of collectors(SIPX and IPETC)and the dosage of methyl-isobutyl-carbonyl(MIBC)as frother on the separation efficiency were evaluated at different pH levels.Based on the analysis of variance(ANOVA),the interaction effects of the collector−pH and collector−frother were significant for the separation efficiency.At the low level of collector dosage,increasing pH from 9 to 11 enhanced copper separation efficiency from 81%to 86%for IPETC and from 77%to 86%for SIPX.Results of ANOVA showed that the maximum copper separation efficiency(88.7%)was obtained at the dosages of 8.6 g/t SIPX,7 g/t IPETC and 20 g/t MIBC at pH 11.Finally,it was concluded that a mixture of SIPX and IPETC collectors was more suitable to treat highly clayey sulphide ores.展开更多
The effect of sulphide(Na2S)concentration(SC)on the corrosion and cavitation erosion behaviours of a cast nickel aluminium bronze(NAB)in 3.5% NaCl solution is investigated in this study.The results show that when the ...The effect of sulphide(Na2S)concentration(SC)on the corrosion and cavitation erosion behaviours of a cast nickel aluminium bronze(NAB)in 3.5% NaCl solution is investigated in this study.The results show that when the SC exceeds 50 ppm,the hydrogen evolution reaction dominates the cathodic process,and a limiting current region appears in the anodic branch of the polarisation curve due to the formation of a copper sulphide film,which is a diffusion-controlled process.After longterm immersion,the increased mass loss rate of NAB with the sulphide additions of 20 and 50 ppm is attributed to the less protective films,which contains a mixture of copper oxides and sulphides.Moreover,NAB undergoes severe localised corrosion(selective phase corrosion,SPC)at the β’phases and eutectoid microstructureα+κⅢ.By comparison,NAB undergoes general corrosion and a copper sulphide film is formed in 100 and 200 ppm sulphide solutions.Cavitation erosion greatly increases the corrosion rate of NAB in all solutions and causes a negative potential shift in 3.5%NaCl solution due to the film destruction.However,a positive potential shift occurs in the solutions with SC higher than 50 ppm due to the accelerated mass transfer of the cathodic process.The cavitation erosion mass loss rate of NAB increases with the increase of SC.The occurrence of severe SPC decreases the phase boundary cohesion and causes brittle fracture under the cavitation impact.The corrosion-enhanced erosion is the most predominant factor for the cavitation erosion damage when the SC exceeds 50 ppm.展开更多
The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching as djurleite〉bomite〉pyritic chalcopyrite〉covellite〉po...The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching as djurleite〉bomite〉pyritic chalcopyrite〉covellite〉porphyry chalcopyfite. The residues were characterized by X-ray diffraction （XRD） and scanning electron microscopy （SEM）. It is indicated that jarosite may not be responsible for hindered disso- lution. The elemental sulfur layer on the surface of pyritic chalcopyrite residues is cracked. The compact surface layer of porphyry chalcopy- rite may strongly hinder copper extraction. X-ray photoelectron spectroscopy （XPS） further confirms that the passivation layers of covellite, pyritic chalcopyrite, and porphyry chalcopyrite are copper-depleted sulphide Cu4S11, S8, and copper-rich iron-deficient polysulphide CtuFe2S9, resoectivelv. The ability of these oassivation layers was found as Cu4Fe2S9〉Cu4S11〉S8〉iarosite.展开更多
Bioleaching of low-grade complex Cu–Zn–Pb–Fe–Ag–Au sulphide concentrate (of Majdanpek ore body, RTB Bor, Serbia) was carried out in an aerated bioleach reactor in the ...Bioleaching of low-grade complex Cu–Zn–Pb–Fe–Ag–Au sulphide concentrate (of Majdanpek ore body, RTB Bor, Serbia) was carried out in an aerated bioleach reactor in the presence of mesophilic mixed bacterial culture of Acidithiobacillus ferrooxidans, Acidithiobacillus thiooxidans, and Leptospirillum ferrooxidans. A mesophilic acidophiles culture was isolated from the acidic solution of the underground copper mine of Bor, Serbia. The nutrient medium was 9K at pH 1.6. 87% of the particles were <10 µm in size, with a pulp density of 8% (w/v). Bioleaching efficiencies of 89% for zinc, 83% for copper, and 68% for iron can be achieved in the examined conditions. Kinetic analysis shows that the change in leaching corresponds to the Spencer-Topley kinetic model for diffusion-controlled topochemical reactions.展开更多
Bacterial community dynamics and copper leaching with applied forced aeration were investigated during low-grade copper sulphide bioleaching to obtain better bioleaching efficiency.Results illustrated that appropriate...Bacterial community dynamics and copper leaching with applied forced aeration were investigated during low-grade copper sulphide bioleaching to obtain better bioleaching efficiency.Results illustrated that appropriate aeration improved bacterial concentrations and leaching efficiencies.The highest bacterial concentration and Cu^(2+)concentration after 14-d leaching were 7.61×10^(7) cells·mL^(−1) and 704.9 mg·L^(−1),respectively,at aeration duration of 4 h·d^(−1).The attached bacteria played a significant role during bioleaching from 1 to 7 d.However,free bacteria dominated the bioleaching processes from 8 to 14 d.This phenomenon was mainly caused by the formation of passivation layer through Fe3+hydrolysis along with bioleaching,which inhibited the contact between the attached bacteria and ore.Meanwhile,16S rDNA analysis verified the effect of Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans on the bioleaching process.The results demonstrate the importance of free and attached bacteria in bioleaching.展开更多
As a promising energy-storage device,the hybrid lithium-ion capacitor coupling with both a large energy density battery-type anode and a high power density capacitor-type cathode is attracting great attention.For the ...As a promising energy-storage device,the hybrid lithium-ion capacitor coupling with both a large energy density battery-type anode and a high power density capacitor-type cathode is attracting great attention.For the sake of improving the energy density of hybrid lithium-ion capacitor,the free-standing anodes with good electrochemical performance are essential.Herein,we design an effective electrospinning strategy to prepare free-standing MnS/Co4S3/Ni3S2/Ni/C-nanofibers(TMSs/Ni/C-NFs)film and firstly use it as a binder-free anode for hybrid lithium-ion capacitor.We find that the carbon nanofibers can availably prevent MnS/Co4S3/Ni3S2/Ni nanoparticles from aggregation as well as significantly improve the electrochemical performance.Therefore,the binder-free TMSs/Ni/C-NFs membrane displays an ultrahigh reversible capacity of 1246.9 m Ah g-1at 100 m A g-1,excellent rate capability(398 mAh g-1 at2000 mA g-1),and long-term cyclic endurance.Besides,we further assemble the hybrid lithium-ion capacitor,which exhibits a high energy density of 182.0 Wh kg-1at 121.1 W kg-1(19.0 Wh kg-1 at 3512.5 W kg-1)and remarkable cycle life.展开更多
Mineral sulphide （MS）-lime （CaO） ion exchange reactions （MS ＋ CaO = MO ＋ CaS） and the effect of CaO/C mole ratio during carbothermic reduction （MS ＋ CaO ＋ C = M ＋ CaS ＋ CO（g）） were investigated for com...Mineral sulphide （MS）-lime （CaO） ion exchange reactions （MS ＋ CaO = MO ＋ CaS） and the effect of CaO/C mole ratio during carbothermic reduction （MS ＋ CaO ＋ C = M ＋ CaS ＋ CO（g）） were investigated for complex froth flotation mineral sulphide concentrates. Phases in the partially and fully reacted samples were characterised by X-ray diffraction （XRD） and scanning electron microscopy （SEM）. The primary phases during mineral sulphide-lime ion exchange reactions are Fe304, CaSO4 Cu2S, and CaS. A complex liquid phase of Ca2CuFeO3S forms during mineral sulphide-lime exchange reactions above 1173 K. The formation mechanisms of Ca2CuFeO3S liquid phase are determined by characterising the partially reacted samples. The reduction rate and extent of mineral sulphides in the presence of CaO and C increase with the increase in CaO/C ratio. The metallic phases are surrounded by the CaS rich phase at CaO/C 〉 1, but the metallic phases and CaS are found as separate phases at CaO/C 〈 1. Experimental results show that the stoichiometric ratio of carbon should be slightly higher than that of CaO. The reactions between CaO and gangue minerals （SiO2 and A1203） are only observed at CaO/C 〉 1 and the reacted samples are excessively sintered.展开更多
We conducted two-stage acidification-bioleaching experiments to probe the feasibility of bioleaching for a kind of mixed alkaline copper oxide and sulphide mineral. We used the uniform design method for data analysis ...We conducted two-stage acidification-bioleaching experiments to probe the feasibility of bioleaching for a kind of mixed alkaline copper oxide and sulphide mineral. We used the uniform design method for data analysis and experimental optimization, with initial pH value, pulp density, inoculation of bacteria and ferrous iron concentration selected as the influential factors. Polynomial regression shows that the four factors sequentially influence the copper recovery by 14.430%, 8.555%, 1.982% and 3.895%. Acid equilibrium in the bioleaching system is mainly influenced by alkaline gangue content, chemical reactions and bacterial activity. A maximal portion of refractory copper extracted reaches 71.08%. The dynamic analysis of copper recovery indicates that bioleaching goes through a lag leaching phase, prime leaching phase and leaching stationary phase corresponding to the growth phases of bacteria. Compared with the predicted value of 80.87%, the confirmatory experiment observes a 78.21% copper recovery under the optimal conditions of pH of 1.5, pulp density of 5%, bacteria inoculation of 30% and initial ferrous iron concentration of 9 g L-1. Results suggest that bioleaching is technically feasible to improving total copper recovery.展开更多
The sulphide capacity of CaO-SiO2-Al2O3-MgO-FetO slags was studied at 1773 K using gas-slag equilibrium techniques. Utilizing a Pt crucible, the slag was equilibrated with a mixture of gases, namely, CO, CO2, SO2 and ...The sulphide capacity of CaO-SiO2-Al2O3-MgO-FetO slags was studied at 1773 K using gas-slag equilibrium techniques. Utilizing a Pt crucible, the slag was equilibrated with a mixture of gases, namely, CO, CO2, SO2 and N2 to provide the partial pressure of oxygen and sulphur. It was shown that at fixed FetO and Al2O3 contents and a fixed { （%CaO）＋（%MgO）}/（%SIO2） ratio, the sulphide capacity decreases with increasing MgO content. At a constant （%CaO）/（%SiO2） ratio and constant MgO and Al2O3 contents, increasing the FetO content of the slags also results in an increase of the sulphide capacity. The rising basicity of （%CaO）/（%SiO2） from 1.0 to 1.4 at fixed MgO, FetO and Al2O3 contents significantly increases the sulphide capacity.展开更多
基金supported by the National Natural Science Foundation of China(No.42177059).
文摘The release of phosphorus(P)from anaerobic sediments becomes the dominant source of P loading with effective control of external P pollution.As a crucial component responsible for binding P,vivianite(Fe_(3)(PO_(4))_(2)·8H_(2)O)in sediment inevitably impacts the P level and transformation.The release of P from vivianite mediated by sulphide was investigated using simulated overlying watersediment and chemical reaction systems.The percentage of redox-stable P in the sediments increased with vivianite input in the overlying watersediment system.Increasing P concentrations in both the overlying water and interstitial water occurred before day 10,accompanied by a decreasing percentage of redox-sensitive P in the sediments driven by sulphide.The continuous release of P from vivianite clarifies the influence of sulphide on promoting vivianite dissolution in a chemical reaction system with vivianite and sulphide solution.Additionally,Mössbauer spectrum and nanoscale secondary ionmass spectrometry(NanoSIMS)images based on the chemical reaction with^(57)Fe isotope labelling demonstrated the presence of initial vivianite,newly produced vivianite,and FeS_(2).
基金Project (50964004) supported by the National Natural Science Foundation of China
文摘The leaching behavior of main metallic sulphides in zinc concentrate under atmospheric oxygen-rich direct leaching conditions was studied through mineralogical analysis. The results show that the sulphides dissolve obviously except pyrite. Based on the relationship between elemental sulfur and the residual sulphides in the leaching residue, the dissolution of sphalerite, chalcopyrite, covellite and galena is assumed to follow the indirect oxidation reactions, where the acidic dissolution takes place firstly and then the released H2S transfers from the mineral surface into bulk solution and is further oxidized into elemental sulfur. The interface chemical reaction is further supposed as the controlling step in the leaching of these sulphides. The direct electrochemical oxidation reactions are assumed to contribute to the dissolution of pyrrhotite, which is controlled by the diffusion through elemental sulfur layer.
文摘The relationships between the sulphide capacity index and the optical basicity, the mole fraction of oxygen ion and the Bell's ratio were investigated based on extensive lab scale equilibrium and industry scale quasi-equilibrium experimental data in the temperature range of 1300 1600℃. Although the sulphide capacity index has good relations with different representations of slag basicity. according to the data obtained under the lab scale equilibrium experimental conditions,the similar relations do not exist according to the data obtained under the industry scale quasi-equilibrium experimental conditions. So it is concluded that the sulphide capacity index, which has been considered as a measure of the slag basicity. can not be used for virtually all oxide slags of interest in the field of ironmaking and steelmaking.
基金This work was supported by grants from the Fondo de Apoyo a la Investigación(UASLP)and Fondos Mixtos Consejo Nacional de Ciencia y Tecnología-Gobierno de San Luis Potosí(Project FMSLP 2002-5630).
文摘The facile chemical synthesis of silver sulphide nanocrystals from metal-loaded organic media, containing a silver-selective organophosphorous ligand as extractant, is reported. The method involves the phase-transfer of silver species from aqueous nitrate media to organic solution using the commercial extractant Cyanex? 471x (tri-isobutylphosphine sulphide, Cytec Co.) as extractant, followed by precipitation stripping using ammonium sulphide as strip reagent. The nanoparticles were structurally characterized, and some aspects of the synthetical process, are briefly discussed. Under the conditions studied, the extractant Cyanex? 471x was able to act as stabilizer adsorbing on the particles surface, maintaining the size of the particles nanometrical.
文摘A logic fault tree of mine spontaneous combustion of sulphide ores was built by the fault tree analysis (FTA) based on a lot of mechanism investigation of sulphide ore spontaneous combustion in more than ten mines and review of a great amount of relevant
基金Projects 2008BAB31B01 supported by the National Key Technology R&D Program in the 11th Five-Year Plan of China50834006 by the National Natural Science Foundation of China
文摘In our study we investigated a refractory copper-nickel sulfide ore separation by using a cyclonic-static micro-bubble flotation column (FCSMC). The process mineralogy of the main products was studied. Using a scanning electron microscope-energy dispersive system (SEM-EDS) and an X-ray spectrometer the mineral category and content of samples were analyzed. By using a mineral liberation analyzer (MLA) the mineral liberation characteristics were revealed. It is shown that in roughing feed the monomers liberation degree of nickel pyrite and chalcopyrite take up 84.11% and 88.82%, respectively. In tailings, the lost nickel pyrite and chalcopyrite are mainly monomers. Therefore, strengthening the micro-fine particle recovery capacity is the key to increase recovery.
文摘The Devonian volcano-passive continental margin in southern Altay is a significant volcanogenic massive sulphide metallogenic belt. Acidic volcanism has been dominant on the inner side of the volcano-passive continental margin, i.e., near the old land, resulting in a Pb-Zn metallogenic sub-belt, in which the ore deposits are hosted by sedimentary rocks in volcanic series, as represented by the large Koktal Pb-Zn deposits. In the central part of the margin far away from the old land, bimodal volcanic formations are well developed, forming volcanics-hosted Cu-Zn metallogenic sub-belts, e.g., the large-scale Ashele Cu-Zn deposit. The Qiaoxiahala sub-belt on the outer side of the margin near the ocean ridge is located at the spreading central trough, where ophiolite suites are developed. This type of deposits is rich in gold and copper, similar to the Cyprus-type Fe-Cu-Au metallogenic sub-belt in metallogenic environment (represented by the Qiaoxiahala medium-scale Fe-Cu-Au deposit). From the old land to the ocean, the mineralizing age becomes younger, i.e., from Early Devonian→Early and Middle Devonian→Middle Devonian, forming a complete metallogenic zoning series on the volcano-passive continental margin. Comparative studies show that the massive sulphide deposits distributed on the volcano-passive continental margin are different from those formed under a plate subduction regime and oceanic ridge environment; the former have their unique features and wide distributions, representing a new type of volcanogenic massive sulphide deposits—the Altay type.
基金the AbbasAbad copper mineShahrood University of Technology for their financial support during this research。
文摘Mechanochemical sulfidization of a mixed sulfide/oxide copper ore by co-grinding with sulfur and additives including Mg(NO3)2 and Fe(NO3)3 salts and iron,aluminum and magnesium powders was investigated for the first time.Also,the influence of sulfidization during the wet-milling process was examined on the separation efficiency and recovery of copper in detail.The results demonstrated that co-grinding with sulfur solely had the best flotation performance at the value of 0.5 wt.%and it was attributed to the possible existence of S\\O bonding on copper oxides surfaces.In addition,adding magnesium nitrate salt,magnesium powder,iron nitrate salt and aluminum powder as additive associated with 0.5 wt%sulfur into ball milling caused the flotation improvement at the amounts of 0.2 wt%,0.2 wt%,0.5 wt%and 0.5 wt%,respectively.Also,the effect of grinding time and sulfidization pH with 0.5 wt%sulfur solely was determined and pH s of 7.5 to 8.5 gave the best results.The highest recovery(75.76%)and separation efficiency(63.44%)were achieved at pH of 7.5 and 8.5,respectively.
文摘Microwave assisted leaching of complex copper sulphide concentrate with ferric chloride was investigated, and its mechanism was analyzed. The results show that the leaching rate by microwave irradiation heating is much faster than that by conventional heating.
文摘Flotation reagents have a complex behaviour in the beneficiation of base minerals in clayey ores.Interaction effects of reagents on the efficiency of copper flotation for a highly clayey low-grade sulphide ore were investigated using a central composite design.Preliminary results showed that sodium-isopropyl-xanthate(SIPX)and O-isopropyl-N-ethyl-thionocarbamate(IPETC)were found to be the most efficient collectors in the presence of lime as the pH regulator.The effects of dosage of collectors(SIPX and IPETC)and the dosage of methyl-isobutyl-carbonyl(MIBC)as frother on the separation efficiency were evaluated at different pH levels.Based on the analysis of variance(ANOVA),the interaction effects of the collector−pH and collector−frother were significant for the separation efficiency.At the low level of collector dosage,increasing pH from 9 to 11 enhanced copper separation efficiency from 81%to 86%for IPETC and from 77%to 86%for SIPX.Results of ANOVA showed that the maximum copper separation efficiency(88.7%)was obtained at the dosages of 8.6 g/t SIPX,7 g/t IPETC and 20 g/t MIBC at pH 11.Finally,it was concluded that a mixture of SIPX and IPETC collectors was more suitable to treat highly clayey sulphide ores.
基金financially supported by the National Natural Science Foundation of China (Nos.51601058 and 51879089)the Fundamental Research Funds for the Central Universities of P.R.China (No.2018B59614)+1 种基金the Natural Science Foundation of Jiangsu Province (BK20191161),the Changzhou Sci & Tech Program (Grant No.CJ20180045)the first group of 2011 plan of China’s Jiangsu province (Grant No.[2013] 56) (Cooperative Innovational Center for Coastal Development & Protection)
文摘The effect of sulphide(Na2S)concentration(SC)on the corrosion and cavitation erosion behaviours of a cast nickel aluminium bronze(NAB)in 3.5% NaCl solution is investigated in this study.The results show that when the SC exceeds 50 ppm,the hydrogen evolution reaction dominates the cathodic process,and a limiting current region appears in the anodic branch of the polarisation curve due to the formation of a copper sulphide film,which is a diffusion-controlled process.After longterm immersion,the increased mass loss rate of NAB with the sulphide additions of 20 and 50 ppm is attributed to the less protective films,which contains a mixture of copper oxides and sulphides.Moreover,NAB undergoes severe localised corrosion(selective phase corrosion,SPC)at the β’phases and eutectoid microstructureα+κⅢ.By comparison,NAB undergoes general corrosion and a copper sulphide film is formed in 100 and 200 ppm sulphide solutions.Cavitation erosion greatly increases the corrosion rate of NAB in all solutions and causes a negative potential shift in 3.5%NaCl solution due to the film destruction.However,a positive potential shift occurs in the solutions with SC higher than 50 ppm due to the accelerated mass transfer of the cathodic process.The cavitation erosion mass loss rate of NAB increases with the increase of SC.The occurrence of severe SPC decreases the phase boundary cohesion and causes brittle fracture under the cavitation impact.The corrosion-enhanced erosion is the most predominant factor for the cavitation erosion damage when the SC exceeds 50 ppm.
文摘The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching as djurleite〉bomite〉pyritic chalcopyrite〉covellite〉porphyry chalcopyfite. The residues were characterized by X-ray diffraction （XRD） and scanning electron microscopy （SEM）. It is indicated that jarosite may not be responsible for hindered disso- lution. The elemental sulfur layer on the surface of pyritic chalcopyrite residues is cracked. The compact surface layer of porphyry chalcopy- rite may strongly hinder copper extraction. X-ray photoelectron spectroscopy （XPS） further confirms that the passivation layers of covellite, pyritic chalcopyrite, and porphyry chalcopyrite are copper-depleted sulphide Cu4S11, S8, and copper-rich iron-deficient polysulphide CtuFe2S9, resoectivelv. The ability of these oassivation layers was found as Cu4Fe2S9〉Cu4S11〉S8〉iarosite.
基金the results of a project approved and funded by the Ministry of Education,Science and Technology Development of the Republic of Serbia(Project Nos.TR 34004 and TR 34024)the EU FP6 BioMinE project by Bioclear,the Netherlands(European project contract NMP2-CT-2005-500329-1)
文摘Bioleaching of low-grade complex Cu–Zn–Pb–Fe–Ag–Au sulphide concentrate (of Majdanpek ore body, RTB Bor, Serbia) was carried out in an aerated bioleach reactor in the presence of mesophilic mixed bacterial culture of Acidithiobacillus ferrooxidans, Acidithiobacillus thiooxidans, and Leptospirillum ferrooxidans. A mesophilic acidophiles culture was isolated from the acidic solution of the underground copper mine of Bor, Serbia. The nutrient medium was 9K at pH 1.6. 87% of the particles were <10 µm in size, with a pulp density of 8% (w/v). Bioleaching efficiencies of 89% for zinc, 83% for copper, and 68% for iron can be achieved in the examined conditions. Kinetic analysis shows that the change in leaching corresponds to the Spencer-Topley kinetic model for diffusion-controlled topochemical reactions.
基金This work was supported by National Science Foundation for Excellent Young Scholars,China(No.51722401)Key Project of National Natural Science Foundation,China(No.51734001)Fundamental Research Funds for the Central Universities(No.FRF-TP-18-003C1).
文摘Bacterial community dynamics and copper leaching with applied forced aeration were investigated during low-grade copper sulphide bioleaching to obtain better bioleaching efficiency.Results illustrated that appropriate aeration improved bacterial concentrations and leaching efficiencies.The highest bacterial concentration and Cu^(2+)concentration after 14-d leaching were 7.61×10^(7) cells·mL^(−1) and 704.9 mg·L^(−1),respectively,at aeration duration of 4 h·d^(−1).The attached bacteria played a significant role during bioleaching from 1 to 7 d.However,free bacteria dominated the bioleaching processes from 8 to 14 d.This phenomenon was mainly caused by the formation of passivation layer through Fe3+hydrolysis along with bioleaching,which inhibited the contact between the attached bacteria and ore.Meanwhile,16S rDNA analysis verified the effect of Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans on the bioleaching process.The results demonstrate the importance of free and attached bacteria in bioleaching.
基金financially supported by the National Natural Science Foundation of China (Grant Nos. 51072173, 51272221 and 51302239)Specialized Research Fund for the Doctoral Program of Higher Education (Grant Nos. 20134301130001)the Natural Science Foundation of Hunan Province, China (Grant Nos. 13JJ4051).
文摘As a promising energy-storage device,the hybrid lithium-ion capacitor coupling with both a large energy density battery-type anode and a high power density capacitor-type cathode is attracting great attention.For the sake of improving the energy density of hybrid lithium-ion capacitor,the free-standing anodes with good electrochemical performance are essential.Herein,we design an effective electrospinning strategy to prepare free-standing MnS/Co4S3/Ni3S2/Ni/C-nanofibers(TMSs/Ni/C-NFs)film and firstly use it as a binder-free anode for hybrid lithium-ion capacitor.We find that the carbon nanofibers can availably prevent MnS/Co4S3/Ni3S2/Ni nanoparticles from aggregation as well as significantly improve the electrochemical performance.Therefore,the binder-free TMSs/Ni/C-NFs membrane displays an ultrahigh reversible capacity of 1246.9 m Ah g-1at 100 m A g-1,excellent rate capability(398 mAh g-1 at2000 mA g-1),and long-term cyclic endurance.Besides,we further assemble the hybrid lithium-ion capacitor,which exhibits a high energy density of 182.0 Wh kg-1at 121.1 W kg-1(19.0 Wh kg-1 at 3512.5 W kg-1)and remarkable cycle life.
基金the financial support by the Copperbelt University in Zambia and the Institute of Materials,Minerals and Mining(IOM~3)
文摘Mineral sulphide （MS）-lime （CaO） ion exchange reactions （MS ＋ CaO = MO ＋ CaS） and the effect of CaO/C mole ratio during carbothermic reduction （MS ＋ CaO ＋ C = M ＋ CaS ＋ CO（g）） were investigated for complex froth flotation mineral sulphide concentrates. Phases in the partially and fully reacted samples were characterised by X-ray diffraction （XRD） and scanning electron microscopy （SEM）. The primary phases during mineral sulphide-lime ion exchange reactions are Fe304, CaSO4 Cu2S, and CaS. A complex liquid phase of Ca2CuFeO3S forms during mineral sulphide-lime exchange reactions above 1173 K. The formation mechanisms of Ca2CuFeO3S liquid phase are determined by characterising the partially reacted samples. The reduction rate and extent of mineral sulphides in the presence of CaO and C increase with the increase in CaO/C ratio. The metallic phases are surrounded by the CaS rich phase at CaO/C 〉 1, but the metallic phases and CaS are found as separate phases at CaO/C 〈 1. Experimental results show that the stoichiometric ratio of carbon should be slightly higher than that of CaO. The reactions between CaO and gangue minerals （SiO2 and A1203） are only observed at CaO/C 〉 1 and the reacted samples are excessively sintered.
基金Funded by the National Natural Science Foundation of China (No. 50934002)New Century Excellent Talents (No. NECT-07-0070)Yunnan Provincial Programs for Science and Technology Innovation (No. 2007AD001)
文摘We conducted two-stage acidification-bioleaching experiments to probe the feasibility of bioleaching for a kind of mixed alkaline copper oxide and sulphide mineral. We used the uniform design method for data analysis and experimental optimization, with initial pH value, pulp density, inoculation of bacteria and ferrous iron concentration selected as the influential factors. Polynomial regression shows that the four factors sequentially influence the copper recovery by 14.430%, 8.555%, 1.982% and 3.895%. Acid equilibrium in the bioleaching system is mainly influenced by alkaline gangue content, chemical reactions and bacterial activity. A maximal portion of refractory copper extracted reaches 71.08%. The dynamic analysis of copper recovery indicates that bioleaching goes through a lag leaching phase, prime leaching phase and leaching stationary phase corresponding to the growth phases of bacteria. Compared with the predicted value of 80.87%, the confirmatory experiment observes a 78.21% copper recovery under the optimal conditions of pH of 1.5, pulp density of 5%, bacteria inoculation of 30% and initial ferrous iron concentration of 9 g L-1. Results suggest that bioleaching is technically feasible to improving total copper recovery.
基金This project was financially supported by the National Natural Science Foundation of China (No.50574036) and Natural Science Foun-dation of HeBei Province, China (No.502267).
文摘The sulphide capacity of CaO-SiO2-Al2O3-MgO-FetO slags was studied at 1773 K using gas-slag equilibrium techniques. Utilizing a Pt crucible, the slag was equilibrated with a mixture of gases, namely, CO, CO2, SO2 and N2 to provide the partial pressure of oxygen and sulphur. It was shown that at fixed FetO and Al2O3 contents and a fixed { （%CaO）＋（%MgO）}/（%SIO2） ratio, the sulphide capacity decreases with increasing MgO content. At a constant （%CaO）/（%SiO2） ratio and constant MgO and Al2O3 contents, increasing the FetO content of the slags also results in an increase of the sulphide capacity. The rising basicity of （%CaO）/（%SiO2） from 1.0 to 1.4 at fixed MgO, FetO and Al2O3 contents significantly increases the sulphide capacity.
