A zinc sulfate open framework matrix,[Zn(SO_4)(DMSO)](1),was synthesized by solvothermal evaporationusing dimethyl sulfoxide(DMSO)as the solvent.A compositeP@1,which exhibits fluorescence and room tempera-ture phospho...A zinc sulfate open framework matrix,[Zn(SO_4)(DMSO)](1),was synthesized by solvothermal evaporationusing dimethyl sulfoxide(DMSO)as the solvent.A compositeP@1,which exhibits fluorescence and room tempera-ture phosphorescence(RTP)properties,was prepared by doping 2,6-naphthalic acid(P)into matrix1at a low con-centration.P@1emitted a green RTP that was visible to the naked eye and lasted for approximately 2 s.P@1exhib-ited selective phosphorescence enhancement response towards Pb2+,with a detection limit of 2.52μmol·L-1.Themain detection mechanism is the Pb—O coordination-induced phosphorescence enhancement in the system.Inter-estingly,P@1also functioned as a dual-channel probe for the rapid detection of Fe3+ions through fluorescencequenching with a detection limit of 0.038μmol·L-1.The recognition mechanism may be attributed to the competi-tive energy absorption betweenP@1and Fe3+ions.CCDC:2388502,1.展开更多
The lime-Cu2+-xanthate process is commonly used for the flotation separation of sphalerite from pyrite.In this process,lime is added to the pulp to inhibit the floatability of pyrite.However,the excessive use of li...The lime-Cu2+-xanthate process is commonly used for the flotation separation of sphalerite from pyrite.In this process,lime is added to the pulp to inhibit the floatability of pyrite.However,the excessive use of lime can result in pipeline blockage and inadequate recovery of associated precious metals.Therefore,it is necessary to develop new flotation process that minimizes or eliminates the use of lime.In this paper,a novel Fe3+-Cu2+-butyl xanthate process was developed as an alternative to lime for separating of sphalerite from pyrite.The flotation results indicated that with the artificially-mixed minerals,the flotation recovery of pyrite was lower than 16%and that of sphalerite was higher than 47%at pH 5.0−10.0.The zeta potential measurements revealed that ferric ion preferred to adsorb on pyrite,and copper ion displaced with zinc ion from the lattice at the interface of sphalerite.The wettability analyses indicated that the hydrophobicity of sphalerite surface increased apparently after being treated with Fe3+-Cu2+-BX,while the hydrophobicity of pyrite surface remained nearly unchanged.With XPS analysis,Cu-S bond and hydrophilic ferric hydroxide were detected separately on the surface of sphalerite and pyrite after conditioning with Fe3+-Cu2+-BX,which facilitated the flotation separation of sphalerite from pyrite with butyl xanthate collector.展开更多
In order to explore the reaction mechanism of Fe^3+ and the mineralization effect of the micropollutant, Fe^3+ assisted photocatalytic oxidation of sulfadiazine (SD) in the TiO2 suspended solution is investigated....In order to explore the reaction mechanism of Fe^3+ and the mineralization effect of the micropollutant, Fe^3+ assisted photocatalytic oxidation of sulfadiazine (SD) in the TiO2 suspended solution is investigated. The effect of Fe^3+ participation, the degradation kinetics of SD, the effect of SD mineralization and the possible mechanism of Fe^3+ participation in TiO2 suspension are analyzed by adding FeCl3, taking samples at a given time and determining the SD concentration. Results indicate that the degradation of SD catalyzed by TiO2/ Fe^3+ is faster than that catalyzed by TiO2 or Fe^3+ separately. The photocatalytic degradation of SD follows the pseudo-first- order kinetics model in a range of 20 to 80 mg/L of initial concentration. The mineralization rate of SD can be enhanced by the addition of Fe^3+ in the TiO2 suspended solution. The mechanism of the rapid degradation of SD is proposed, which indicates that Fe^3+ adsorbed on the surface of TiO2 particles acts as an electron acceptor. The amount of recombining electronhole pairs decreases, and the amount of hydroxyl radicals increases. The increased hydroxyl radical strengthens the degradation of SD in the TiO2/Fe^3+ suspended solution.展开更多
A series of catalysts were prepared by doping different loadings of CeO2 over TiO2-SiO2-WO3 and used for the selective catalytic reduction of NOx by NH3. The experimental results showed that the selective catalytic re...A series of catalysts were prepared by doping different loadings of CeO2 over TiO2-SiO2-WO3 and used for the selective catalytic reduction of NOx by NH3. The experimental results showed that the selective catalytic reduction(SCR) performance and SO2-resistant ability of TiO2-SiO2-WO3 were greatly enhanced by the introduction of cerium. The catalyst containing 10% CeO2 showed the highest NO conversion in a wide temperature range and good N2 selectivity with broad operation temperature window at the gas hourly space velocity(GHSV) of 30000 h–1, which was a very promising catalyst for NOx abatement from diesel engine exhaust. The catalysts were characterized by X-ray diffraction(XRD), scanning electron microscopy with energy dispersive X-ray spectroscopy(SEM-EDS), N2 adsorption-desorption(BET) and X-ray photoelectron spectroscopy(XPS). The characterization results showed that the bigger pore radius, higher surface atomic concentration and dispersion of Ce and the abundant adsorbed oxygen on the surface of catalyst contributed to the best NH3-SCR performance of CeO2/TiO2-SiO2-WO3 catalyst containing 10% CeO2.展开更多
SiO2 coated Ce2S3 red pigment was prepared in ethanol/H2O system via sol-gel method and TEOS were used as silica sources. X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy...SiO2 coated Ce2S3 red pigment was prepared in ethanol/H2O system via sol-gel method and TEOS were used as silica sources. X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDX), UV-visible spectro-photometer and automatic colorimeter were used to investigate the properties of the samples. The results showed that the compact SiO2 film formed on the surface of Ce2S3 pigment at a cerium silicon molar ratio of 2. The thermal stability temperature of Ce2S3 pigment was improved to 450 oC after SiO2 coating. In addition, the color of Ce2S3 pigment was not affected significantly through coating colorless and transparent SiO2 and it could be used as safe red pigment in higher temperature fields.展开更多
摘要A zinc sulfate open framework matrix,[Zn(SO_4)(DMSO)](1),was synthesized by solvothermal evaporationusing dimethyl sulfoxide(DMSO)as the solvent.A compositeP@1,which exhibits fluorescence and room tempera-ture phosphorescence(RTP)properties,was prepared by doping 2,6-naphthalic acid(P)into matrix1at a low con-centration.P@1emitted a green RTP that was visible to the naked eye and lasted for approximately 2 s.P@1exhib-ited selective phosphorescence enhancement response towards Pb2+,with a detection limit of 2.52μmol·L-1.Themain detection mechanism is the Pb—O coordination-induced phosphorescence enhancement in the system.Inter-estingly,P@1also functioned as a dual-channel probe for the rapid detection of Fe3+ions through fluorescencequenching with a detection limit of 0.038μmol·L-1.The recognition mechanism may be attributed to the competi-tive energy absorption betweenP@1and Fe3+ions.CCDC:2388502,1.
基金Project(52204363)supported by the National Natural Science Foundation of ChinaProject(2024JJ8042)supported by the Hunan Natural Science Foundation,ChinaProject(22C0220)supported by the Education Department of Hunan Province,China。
摘要The lime-Cu2+-xanthate process is commonly used for the flotation separation of sphalerite from pyrite.In this process,lime is added to the pulp to inhibit the floatability of pyrite.However,the excessive use of lime can result in pipeline blockage and inadequate recovery of associated precious metals.Therefore,it is necessary to develop new flotation process that minimizes or eliminates the use of lime.In this paper,a novel Fe3+-Cu2+-butyl xanthate process was developed as an alternative to lime for separating of sphalerite from pyrite.The flotation results indicated that with the artificially-mixed minerals,the flotation recovery of pyrite was lower than 16%and that of sphalerite was higher than 47%at pH 5.0−10.0.The zeta potential measurements revealed that ferric ion preferred to adsorb on pyrite,and copper ion displaced with zinc ion from the lattice at the interface of sphalerite.The wettability analyses indicated that the hydrophobicity of sphalerite surface increased apparently after being treated with Fe3+-Cu2+-BX,while the hydrophobicity of pyrite surface remained nearly unchanged.With XPS analysis,Cu-S bond and hydrophilic ferric hydroxide were detected separately on the surface of sphalerite and pyrite after conditioning with Fe3+-Cu2+-BX,which facilitated the flotation separation of sphalerite from pyrite with butyl xanthate collector.
基金The Priority Academic Program Development of Jiangsu Higher Education Institutions (No. 1105007001 )the Ph. D. Programs Foundation of Ministry of Education of China (No. 20100092120018)the Natural Science Foundation of Jiangsu Province (No. BK2009453)
摘要In order to explore the reaction mechanism of Fe^3+ and the mineralization effect of the micropollutant, Fe^3+ assisted photocatalytic oxidation of sulfadiazine (SD) in the TiO2 suspended solution is investigated. The effect of Fe^3+ participation, the degradation kinetics of SD, the effect of SD mineralization and the possible mechanism of Fe^3+ participation in TiO2 suspension are analyzed by adding FeCl3, taking samples at a given time and determining the SD concentration. Results indicate that the degradation of SD catalyzed by TiO2/ Fe^3+ is faster than that catalyzed by TiO2 or Fe^3+ separately. The photocatalytic degradation of SD follows the pseudo-first- order kinetics model in a range of 20 to 80 mg/L of initial concentration. The mineralization rate of SD can be enhanced by the addition of Fe^3+ in the TiO2 suspended solution. The mechanism of the rapid degradation of SD is proposed, which indicates that Fe^3+ adsorbed on the surface of TiO2 particles acts as an electron acceptor. The amount of recombining electronhole pairs decreases, and the amount of hydroxyl radicals increases. The increased hydroxyl radical strengthens the degradation of SD in the TiO2/Fe^3+ suspended solution.
基金supported by the National Natural Science Foundation of China(21173153)the National High Technology Research and Development Program of China(863 project)(2013AA065304)
摘要A series of catalysts were prepared by doping different loadings of CeO2 over TiO2-SiO2-WO3 and used for the selective catalytic reduction of NOx by NH3. The experimental results showed that the selective catalytic reduction(SCR) performance and SO2-resistant ability of TiO2-SiO2-WO3 were greatly enhanced by the introduction of cerium. The catalyst containing 10% CeO2 showed the highest NO conversion in a wide temperature range and good N2 selectivity with broad operation temperature window at the gas hourly space velocity(GHSV) of 30000 h–1, which was a very promising catalyst for NOx abatement from diesel engine exhaust. The catalysts were characterized by X-ray diffraction(XRD), scanning electron microscopy with energy dispersive X-ray spectroscopy(SEM-EDS), N2 adsorption-desorption(BET) and X-ray photoelectron spectroscopy(XPS). The characterization results showed that the bigger pore radius, higher surface atomic concentration and dispersion of Ce and the abundant adsorbed oxygen on the surface of catalyst contributed to the best NH3-SCR performance of CeO2/TiO2-SiO2-WO3 catalyst containing 10% CeO2.
基金Project supported by National Science and Technology Support Program(2011BAE30B03)Special Fund from Shaanxi Provincial Department of Education(12JK0467the Graduate Innovation Fund of Shaanxi Universityof Science and Technology for the financial support
摘要SiO2 coated Ce2S3 red pigment was prepared in ethanol/H2O system via sol-gel method and TEOS were used as silica sources. X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDX), UV-visible spectro-photometer and automatic colorimeter were used to investigate the properties of the samples. The results showed that the compact SiO2 film formed on the surface of Ce2S3 pigment at a cerium silicon molar ratio of 2. The thermal stability temperature of Ce2S3 pigment was improved to 450 oC after SiO2 coating. In addition, the color of Ce2S3 pigment was not affected significantly through coating colorless and transparent SiO2 and it could be used as safe red pigment in higher temperature fields.