A series of attapulgite （ATP） supported perovskite-type La1-xCexMnO3 ix=0-0.2） nanocomposites were prepared by a sol-gel method. The samples were characterized by X-ray diffraction, transmission elec- tron microsco...A series of attapulgite （ATP） supported perovskite-type La1-xCexMnO3 ix=0-0.2） nanocomposites were prepared by a sol-gel method. The samples were characterized by X-ray diffraction, transmission elec- tron microscopy, Fourier-transform infrared spectroscopy, H2 temperature-programmed reduction, and temperature-programmed desorption of NH3. Their selective catalytic reduction of NO with NH3 was evaluated in the low-temperature range. The impact of the doping fraction of Ce4＋ on the NO conversion was investigated. The results indicated that the La1-xCexMnO3 nanoparticles with a size of ca. 15 nm were uniformly immobilized on the surface of ATP with a loading amount of 20wt%. The highest conversion rate of NO reached 98.6% when the doping fraction x was O.1, while the ATP support supplied a high surface areas facilitating the nanoparticles dispersion as well as the gas adsorption. Incorporation of an appropriate amount of Ce4＋ in the La3＋ site resulted in a high degree of reduction by the active perovskite species with enhanced catalytic activity.展开更多
文摘A series of attapulgite （ATP） supported perovskite-type La1-xCexMnO3 ix=0-0.2） nanocomposites were prepared by a sol-gel method. The samples were characterized by X-ray diffraction, transmission elec- tron microscopy, Fourier-transform infrared spectroscopy, H2 temperature-programmed reduction, and temperature-programmed desorption of NH3. Their selective catalytic reduction of NO with NH3 was evaluated in the low-temperature range. The impact of the doping fraction of Ce4＋ on the NO conversion was investigated. The results indicated that the La1-xCexMnO3 nanoparticles with a size of ca. 15 nm were uniformly immobilized on the surface of ATP with a loading amount of 20wt%. The highest conversion rate of NO reached 98.6% when the doping fraction x was O.1, while the ATP support supplied a high surface areas facilitating the nanoparticles dispersion as well as the gas adsorption. Incorporation of an appropriate amount of Ce4＋ in the La3＋ site resulted in a high degree of reduction by the active perovskite species with enhanced catalytic activity.
