The integration of surface filtration and catalytic decomposition functions in catalytic bags enables the synergistic removal of multiple pollutants(such as dust,nitrogen oxide,acid gases,and dioxins)in a single react...The integration of surface filtration and catalytic decomposition functions in catalytic bags enables the synergistic removal of multiple pollutants(such as dust,nitrogen oxide,acid gases,and dioxins)in a single reactor,thus effectively reducing the cost and operational difficulties associated with flue gas treatment.In this study,Mn-Ce-Sm-Sn(MCSS)catalysts were prepared and loaded onto hightemperature resistant polyimide(P84)filter through ultrasonic impregnation to create composite catalytic filter.The results demonstrate that the NO conversion rates of the composite catalytic filter consistently achieve above 95%within the temperature range of 160-260℃,with a chlorobenzene T_(90)value of 230℃.The ultrasonic impregnation method effectively loaded the catalyst onto the filter,ensuring high dispersion both on the surface and inside the filter.This increased exposure of catalyst active sites enhances the catalytic activity of the composite catalytic filter.Additionally,increasing the catalyst loading leads to a gradual decrease in permeability,an increase in pressure drops and the long residence time of the flue gas,thereby improving catalytic activity.Compared to ordinary impregnation methods,ultrasonic impregnation improves the bonding strength between the catalyst and filter,as well as the permeability of the composite catalytic filter under the same loading conditions.Overall,this study presents a novel approach to prepare composite catalytic filter for the simultaneous removal of NO and chlorobenzene at low temperatures.展开更多
It has been challenging for Fe(Ⅲ)regeneration in Fe-based photocatalysts for continuous peroxydisulfate(PDS)activation due to the lower ability to reduce Fe(Ⅲ).In this work,Fe-doped ultrathin VO_(2)(Fe-VO_(2))nanobe...It has been challenging for Fe(Ⅲ)regeneration in Fe-based photocatalysts for continuous peroxydisulfate(PDS)activation due to the lower ability to reduce Fe(Ⅲ).In this work,Fe-doped ultrathin VO_(2)(Fe-VO_(2))nanobelts were synthesized for purifying metronidazole(MNZ)via PDS activation.As an efficient Fentonlike catalyst for PDS activation,2 wt%Fe-doped VO_(2)can remove 98%of MNZ within 40 min and exhibits impressive recyclability.The synergistic effect of Fe-VO_(2)and Fe(Ⅲ)activated PDS boosted the photocatalytic performance.Moreover,SO_(4)•^(−),h+,O_(2)•^(−),^(1)O_(2),and•OH were the main reactive radicals.The effects of initial MNZ concentration,Fe-VO_(2),PDS dosage,and various anions/cations on MNZ removal by the Fe-VO_(2)/PDS/Vis system were studied.The intermediates of MNZ degradation and possible pathways were determined by density function theory(DFT)calculations and HPLC-MS.This study provided a sustainable technology using Fe-doped ultrathin VO_(2)nanobelts for photocatalytic PDS activation and decontamination of pharmaceutical wastewater.展开更多
Soil remediation containing numerous organic contaminants is of great significance to ecological environment.Herein,the synergetic effects of Ce-Mn/Al_(2)O_(3)with different active components on catalytic thermal deso...Soil remediation containing numerous organic contaminants is of great significance to ecological environment.Herein,the synergetic effects of Ce-Mn/Al_(2)O_(3)with different active components on catalytic thermal desorption of chlorobenzene in soil were investigated.The optimized Ce-Mn/Al_(2)O_(3)drastically enhance the desorption efficiency of chlorobenzene,and the corresponding conversion reaches 100%within 1 h at a low temperature of 120℃.The superior performance is ascribed to the formation of Ce-Mn solid solution during the calcination process,resulting in a certain lattice change to the generation of abundant oxygen vacancies and acidic sites.Combining with the analysis of in-situ diffuse reflectance infrared spectroscopy and gas chromatography-mass spectrometry,the final products of chlorobenzene are decomposed into CO_(2),H_(2)O,Cl_(2)and HCl.This work sheds light on the rational design of highly-active catalysts for practical applications of sustainable soil remediation.展开更多
Sulfur dioxide is one of the main causes of air pollution such as acid rain and photochemical smog,and its pollution control and resource utilization become an important research direction of air pollution control,The...Sulfur dioxide is one of the main causes of air pollution such as acid rain and photochemical smog,and its pollution control and resource utilization become an important research direction of air pollution control,The active component La-Ce-O_(x) is loaded on SiO_(2),γ-Al_(2)O_(3),TiO_(2) and ZrO_(2),and the La-Ce-Ox@ZrO_(2)exhibits the best catalytic activity.By adjusting the loading amount of La-Ce-O_(x),La-Ce-Ox@ZrO_(2) with different mass fractions was prepared.The results show that the activity of 15%La-Ce-Ox@ZrO_(2)catalyst is the best.The SO_(2)conversion is 100%,and the S yield and S selectivity are more than 96% at 350℃.According to the analysis results of H_(2)-TPR,CO_(2)-TPD and NH_(3)-TPD,ZrO_(2) as a support not only reduces the acidity of the catalyst,but also improves the weak alkaline sites of the catalyst,which is conducive to the adsorption and activation of SO2molecules at low temperature.The incorporation of La and Ce increases the oxygen concentration adsorbed on the catalyst.The strong interaction between the support ZrO_(2) and the active component La-Ce-Oxis conducive to the electron transfer between the active component and the support,and improves the activity of the catalyst.For the 15%La-Ce-O_(x)@ZrO_(2),the main reaction intermediates are weakly adsorbed SO_(2)(SO_(3)^(2-)),bicoordinated CO_(3)^(2-),monodentate carbonate and CO in the gas phase.Therefore,the catalytic reaction follows both L-H and E-R mechanisms.展开更多
基金Project supported by the National Key Research and Development Program of China(2021YFB3500600,2021YFB3500605)Natural Science Foundation of Jiangsu Province(BK20220365)+5 种基金Key R&D Program of Jiangsu Province(BE2022142)Natural Science Foundation of the Jiangsu Higher Education Institutions of China(22KJB610002)Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)the Postgraduate Research&Practice Innovation Program of Jiangsu Province(KYCX23_1419)Science and Technology Plan of Yangzhou(YZ2022030,YZ2023020)the State Key Laboratory of Clean and Efficient Coal-fired Power Generation and Pollution Control(D2022FK098)。
文摘The integration of surface filtration and catalytic decomposition functions in catalytic bags enables the synergistic removal of multiple pollutants(such as dust,nitrogen oxide,acid gases,and dioxins)in a single reactor,thus effectively reducing the cost and operational difficulties associated with flue gas treatment.In this study,Mn-Ce-Sm-Sn(MCSS)catalysts were prepared and loaded onto hightemperature resistant polyimide(P84)filter through ultrasonic impregnation to create composite catalytic filter.The results demonstrate that the NO conversion rates of the composite catalytic filter consistently achieve above 95%within the temperature range of 160-260℃,with a chlorobenzene T_(90)value of 230℃.The ultrasonic impregnation method effectively loaded the catalyst onto the filter,ensuring high dispersion both on the surface and inside the filter.This increased exposure of catalyst active sites enhances the catalytic activity of the composite catalytic filter.Additionally,increasing the catalyst loading leads to a gradual decrease in permeability,an increase in pressure drops and the long residence time of the flue gas,thereby improving catalytic activity.Compared to ordinary impregnation methods,ultrasonic impregnation improves the bonding strength between the catalyst and filter,as well as the permeability of the composite catalytic filter under the same loading conditions.Overall,this study presents a novel approach to prepare composite catalytic filter for the simultaneous removal of NO and chlorobenzene at low temperatures.
基金the financial supports from the National Key Research and Development Program of China(Nos.2021YFB3500600,2021YFB3500605,2022YFB3504100)Key R&D Program of Jiangsu Province(No.BE2022142)+6 种基金Ministry of Education Chunhui plan international cooperation project(No.202200554)National Natural Science Foundation of China(No.grant 22208170)Natural Science Foundation of Inner Mongolia(No.2021BS02016)Jiangsu International Cooperation Project(No.BZ2021018)Nanjing Science and Technology Top Experts Gathering Plan,and Open Foundation of State Environmental Protection Key Laboratory of Soil Environmental Management and Pollution Control(No.SEMPC2023004)Cooperation Foundation for the Chunhui Plan Program of Ministry of Education of China(No.202200554)Open Project Program of Key Laboratory of Opticelectric Sensing and Analytical Chemistry for Life Science(No.M2024-7),MOE。
文摘It has been challenging for Fe(Ⅲ)regeneration in Fe-based photocatalysts for continuous peroxydisulfate(PDS)activation due to the lower ability to reduce Fe(Ⅲ).In this work,Fe-doped ultrathin VO_(2)(Fe-VO_(2))nanobelts were synthesized for purifying metronidazole(MNZ)via PDS activation.As an efficient Fentonlike catalyst for PDS activation,2 wt%Fe-doped VO_(2)can remove 98%of MNZ within 40 min and exhibits impressive recyclability.The synergistic effect of Fe-VO_(2)and Fe(Ⅲ)activated PDS boosted the photocatalytic performance.Moreover,SO_(4)•^(−),h+,O_(2)•^(−),^(1)O_(2),and•OH were the main reactive radicals.The effects of initial MNZ concentration,Fe-VO_(2),PDS dosage,and various anions/cations on MNZ removal by the Fe-VO_(2)/PDS/Vis system were studied.The intermediates of MNZ degradation and possible pathways were determined by density function theory(DFT)calculations and HPLC-MS.This study provided a sustainable technology using Fe-doped ultrathin VO_(2)nanobelts for photocatalytic PDS activation and decontamination of pharmaceutical wastewater.
基金Project supported by the National Key Research and Development Program of China(2021YFB3500600,2021YFB3500605,2022YFB3504100)Key R&D Program of Jiangsu Province(BE2022142)+2 种基金Natural Science Foundation of Jiangsu Province(BK20220365)Jiangsu International Cooperation Project(BZ2021018)Chunhui Project Foundation of the Education Department of China(202200554)。
文摘Soil remediation containing numerous organic contaminants is of great significance to ecological environment.Herein,the synergetic effects of Ce-Mn/Al_(2)O_(3)with different active components on catalytic thermal desorption of chlorobenzene in soil were investigated.The optimized Ce-Mn/Al_(2)O_(3)drastically enhance the desorption efficiency of chlorobenzene,and the corresponding conversion reaches 100%within 1 h at a low temperature of 120℃.The superior performance is ascribed to the formation of Ce-Mn solid solution during the calcination process,resulting in a certain lattice change to the generation of abundant oxygen vacancies and acidic sites.Combining with the analysis of in-situ diffuse reflectance infrared spectroscopy and gas chromatography-mass spectrometry,the final products of chlorobenzene are decomposed into CO_(2),H_(2)O,Cl_(2)and HCl.This work sheds light on the rational design of highly-active catalysts for practical applications of sustainable soil remediation.
基金Project supported by the National Key Research and Development Program of China (2021YFB3500600,2021YFB3500605)Natural Science Foundation of Jiangsu Province (BK20220365)+5 种基金Key R&D Program of Jiangsu Province (BE2022142)Industry-University-Research Cooperation Project of Jiangsu Province (BY2022514)Natural Science Foundation of the Jiangsu Higher Education Institutions of China (22KJB610002)Jiangsu International Cooperation Project(BZ2021018)Jiangsu Funding Program for Excellent Postdoctoral Talent(2022ZB375)Nanjing Science and Technology Top Experts Gathering Plan and the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)。
文摘Sulfur dioxide is one of the main causes of air pollution such as acid rain and photochemical smog,and its pollution control and resource utilization become an important research direction of air pollution control,The active component La-Ce-O_(x) is loaded on SiO_(2),γ-Al_(2)O_(3),TiO_(2) and ZrO_(2),and the La-Ce-Ox@ZrO_(2)exhibits the best catalytic activity.By adjusting the loading amount of La-Ce-O_(x),La-Ce-Ox@ZrO_(2) with different mass fractions was prepared.The results show that the activity of 15%La-Ce-Ox@ZrO_(2)catalyst is the best.The SO_(2)conversion is 100%,and the S yield and S selectivity are more than 96% at 350℃.According to the analysis results of H_(2)-TPR,CO_(2)-TPD and NH_(3)-TPD,ZrO_(2) as a support not only reduces the acidity of the catalyst,but also improves the weak alkaline sites of the catalyst,which is conducive to the adsorption and activation of SO2molecules at low temperature.The incorporation of La and Ce increases the oxygen concentration adsorbed on the catalyst.The strong interaction between the support ZrO_(2) and the active component La-Ce-Oxis conducive to the electron transfer between the active component and the support,and improves the activity of the catalyst.For the 15%La-Ce-O_(x)@ZrO_(2),the main reaction intermediates are weakly adsorbed SO_(2)(SO_(3)^(2-)),bicoordinated CO_(3)^(2-),monodentate carbonate and CO in the gas phase.Therefore,the catalytic reaction follows both L-H and E-R mechanisms.
