Hexagonal CePO4 nanorods were prepared by a precipitation method and hexagonal CePO4 nanowires were prepared by hydrothermal synthesis at 150 ℃. Rh （NO3）3 was then used as a precursor for the impregnation of Rh203 ...Hexagonal CePO4 nanorods were prepared by a precipitation method and hexagonal CePO4 nanowires were prepared by hydrothermal synthesis at 150 ℃. Rh （NO3）3 was then used as a precursor for the impregnation of Rh203 onto these CePO4 materials. The Rh203 supported on the CePO4 nanowires was much more active for the catalytic decomposition of N20 than the RhzO3 supported on CePO4 nanorods. The stability of both catalysts as a function of time on stream was studied and the influence of the co-feed （CO2, O2, H20 or O2/H20） on the N20 decomposition was also investigated. The samples were characterized by N2 adsorption-desorption, induc- tively coupled plasma optical emission spectroscopy, X- ray diffraction, transmission electron microscopy, X-ray photoelectron microscopy, hydrogen temperature-pro- grammed reduction, oxygen temperature-programmed desorption, and CO2 temperature-programmed desorption in order to correlate the physicochemical and catalytic properties.展开更多
文摘Hexagonal CePO4 nanorods were prepared by a precipitation method and hexagonal CePO4 nanowires were prepared by hydrothermal synthesis at 150 ℃. Rh （NO3）3 was then used as a precursor for the impregnation of Rh203 onto these CePO4 materials. The Rh203 supported on the CePO4 nanowires was much more active for the catalytic decomposition of N20 than the RhzO3 supported on CePO4 nanorods. The stability of both catalysts as a function of time on stream was studied and the influence of the co-feed （CO2, O2, H20 or O2/H20） on the N20 decomposition was also investigated. The samples were characterized by N2 adsorption-desorption, induc- tively coupled plasma optical emission spectroscopy, X- ray diffraction, transmission electron microscopy, X-ray photoelectron microscopy, hydrogen temperature-pro- grammed reduction, oxygen temperature-programmed desorption, and CO2 temperature-programmed desorption in order to correlate the physicochemical and catalytic properties.
