A novel Ce-Y/SBA-15 catalyst was prepared by modifying HY/SBA-15 microporous-mesoporous composite molecular sieve with cerium using the impregnation method. The characterization results from scanning electron microsco...A novel Ce-Y/SBA-15 catalyst was prepared by modifying HY/SBA-15 microporous-mesoporous composite molecular sieve with cerium using the impregnation method. The characterization results from scanning electron microscopy/energy dispersive X-ray dispersive spectroscopy（SEM/EDS）, transmission electron microscopy（TEM）, and X-ray fluorescence（XRF） studies indicated that the Ce-modified catalyst maintained the microporous-mesoporous structure of Y/SBA-15. The Ce ions were found to be uniformly dispersed in the pores of the molecular sieve without aggregation. The results from pyrolysis coupled-Fourier transform infrared spectroscopy（Pyridine-FTIR） and temperature programmed desorption of ammonia（NH3-TPD） showed that the loading of cerium caused the hydroxyl group in the catalyst to display stronger Bronsted acidity. The efficiency of the modified Ce-Y/SBA-15 catalyst was evaluated by using it to catalyze the synthesis of n-butyl acetate. The optimal synthesis conditions were determined by orthogonal experiments. The highest esterification yield of 94.4% was obtained when the reaction time was 2.0 h, with acid/alcohol molar ratio of 1：1.2, and catalyst loading of 10 wt.%. The results in this study demonstrated that the loading of cerium and the structure of Y/SBA-15 microporous-mesoporous composite molecular sieve helped in improving the catalytic activity of this acidic catalyst.展开更多
In this study, we investigated the effect of the addition of Sr （0wt%, 0. lwt%, 0.2wt%, and 0.3wt%） on the microstaalcture and cor- rosion behavior of A13Ti/ADC12 composite by optical microscopy, X-ray diffraction, ...In this study, we investigated the effect of the addition of Sr （0wt%, 0. lwt%, 0.2wt%, and 0.3wt%） on the microstaalcture and cor- rosion behavior of A13Ti/ADC12 composite by optical microscopy, X-ray diffraction, sca^lning electron microscopy, mid energy diffraction spectroscopy. The results reveal that the c^-A1 phases were nearly spherical mid 40 gin in size and that the eutectic Si phases became round in the composite when the Sr content reached 0.2wt%. The A13Ti paxticles were distributed uniformly at the grain boundary. The results of the corrosion examination reveal that the A13Ti/ADC12 composite exhibited a minimum corrosion rate of 0.081 g.m 2,hl for an Sr content of 0.2wt%, which is two thirds of that of umnodified composite （0.134 g.m4.h 1）. This improved corrosion resistaalce was due to galvamc cor- rosion, which resulted from the low area ratio of the cathode to anode regions. This caused a low-density corrosion current in the composite, thereby yielding optimum corrosion resistmlce.展开更多
Ce0.8Sm0.2O1.9-δ-La0.9Sr0.1Ga0.8Mg0.2O3-δ（SDC-LSGM）is prepared by the glycine-nitrate process（GNP）.SDC-LSGM composite electrolyte samples with different weight ratios are prepared by the co-combustion method so ...Ce0.8Sm0.2O1.9-δ-La0.9Sr0.1Ga0.8Mg0.2O3-δ（SDC-LSGM）is prepared by the glycine-nitrate process（GNP）.SDC-LSGM composite electrolyte samples with different weight ratios are prepared by the co-combustion method so as to obtain homogeneous nano-sized precursor powders. The X-ray diffraction （XRD） and the scan electron microscope （SEM） are used to investigate the phases and microstructures. The measurements and analyses of oxygen ionic conductivity of SDC-LSGM are carried out through the four-terminal direct current （DC） method and the electrochemical impendence spectroscopy, respectively. The optimum weight ratio of SDC-LSGM is 8∶2, of which the ionic conductivity is 0.113 S/cm at 800℃ and the conductivity activation energy is 0.620 eV. The impendence spectra shows that the grain boundary resistance becomes the main barrier for the ionic conductivity of electrolyte at lower temperatures. The appropriate introduction of LSGM to the electrolyte SDC can not only decrease the electronic conductivity but also improve the conditions of the grain and grain boundary, which is advantageous to cause an increase in oxygen ionic conductivity.展开更多
基金Project supported by the Research Fund for the Doctoral Program of Higher Education(20100042110008)the Talent Scientific Research Fund of Liaoning Shihua University
文摘A novel Ce-Y/SBA-15 catalyst was prepared by modifying HY/SBA-15 microporous-mesoporous composite molecular sieve with cerium using the impregnation method. The characterization results from scanning electron microscopy/energy dispersive X-ray dispersive spectroscopy（SEM/EDS）, transmission electron microscopy（TEM）, and X-ray fluorescence（XRF） studies indicated that the Ce-modified catalyst maintained the microporous-mesoporous structure of Y/SBA-15. The Ce ions were found to be uniformly dispersed in the pores of the molecular sieve without aggregation. The results from pyrolysis coupled-Fourier transform infrared spectroscopy（Pyridine-FTIR） and temperature programmed desorption of ammonia（NH3-TPD） showed that the loading of cerium caused the hydroxyl group in the catalyst to display stronger Bronsted acidity. The efficiency of the modified Ce-Y/SBA-15 catalyst was evaluated by using it to catalyze the synthesis of n-butyl acetate. The optimal synthesis conditions were determined by orthogonal experiments. The highest esterification yield of 94.4% was obtained when the reaction time was 2.0 h, with acid/alcohol molar ratio of 1：1.2, and catalyst loading of 10 wt.%. The results in this study demonstrated that the loading of cerium and the structure of Y/SBA-15 microporous-mesoporous composite molecular sieve helped in improving the catalytic activity of this acidic catalyst.
基金financially supported by the National Natural Science Foundation of China(No.51364035)the Natural Science Foundation of Jiangxi Province(No.20171BAB206034)
文摘In this study, we investigated the effect of the addition of Sr （0wt%, 0. lwt%, 0.2wt%, and 0.3wt%） on the microstaalcture and cor- rosion behavior of A13Ti/ADC12 composite by optical microscopy, X-ray diffraction, sca^lning electron microscopy, mid energy diffraction spectroscopy. The results reveal that the c^-A1 phases were nearly spherical mid 40 gin in size and that the eutectic Si phases became round in the composite when the Sr content reached 0.2wt%. The A13Ti paxticles were distributed uniformly at the grain boundary. The results of the corrosion examination reveal that the A13Ti/ADC12 composite exhibited a minimum corrosion rate of 0.081 g.m 2,hl for an Sr content of 0.2wt%, which is two thirds of that of umnodified composite （0.134 g.m4.h 1）. This improved corrosion resistaalce was due to galvamc cor- rosion, which resulted from the low area ratio of the cathode to anode regions. This caused a low-density corrosion current in the composite, thereby yielding optimum corrosion resistmlce.
基金The National Basic Research Program of China (973 Program) (No.2007CB936300)the Natural Science Foundation of Jiangsu Province (No.BK2009293)
文摘Ce0.8Sm0.2O1.9-δ-La0.9Sr0.1Ga0.8Mg0.2O3-δ（SDC-LSGM）is prepared by the glycine-nitrate process（GNP）.SDC-LSGM composite electrolyte samples with different weight ratios are prepared by the co-combustion method so as to obtain homogeneous nano-sized precursor powders. The X-ray diffraction （XRD） and the scan electron microscope （SEM） are used to investigate the phases and microstructures. The measurements and analyses of oxygen ionic conductivity of SDC-LSGM are carried out through the four-terminal direct current （DC） method and the electrochemical impendence spectroscopy, respectively. The optimum weight ratio of SDC-LSGM is 8∶2, of which the ionic conductivity is 0.113 S/cm at 800℃ and the conductivity activation energy is 0.620 eV. The impendence spectra shows that the grain boundary resistance becomes the main barrier for the ionic conductivity of electrolyte at lower temperatures. The appropriate introduction of LSGM to the electrolyte SDC can not only decrease the electronic conductivity but also improve the conditions of the grain and grain boundary, which is advantageous to cause an increase in oxygen ionic conductivity.
基金National Natural Science Foundation of China(51364035)Ministry of Education Tied up with the Special Research Fund for the Doctoral Program for Higher School(20133601110001)
