Promotive effect of H2O on low-temperature NO reduction by CO over Pd/La0.9Ba0.1AlO3-δ

被引:11
|
作者
Higo, Takuma [1 ]
Omori, Yuki [1 ]
Shigemoto, Ayaka [1 ]
Ueno, Kohei [1 ]
Ogo, Shuhei [1 ]
Sekine, Yasushi [1 ]
机构
[1] Waseda Univ, Dept Appl Chem, Shinjuku Ku, 3-4-1 Okubo, Tokyo 1698555, Japan
关键词
Effect of water; Lattice oxygen; NO reduction by CO; Pd catalyst; SELECTIVE REDUCTION; WATER-VAPOR; CATALYTIC-ACTIVITY; COEXISTING H2O; N2O REDUCTION; PD; STABILITY; STORAGE; OXIDE; GAS;
D O I
10.1016/j.cattod.2019.10.025
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
For future removal of NOx by catalysts, low-temperature NO reduction is desired. Results confirmed that a drastic improvement of catalytic activity by H2O on NO-CO-O-2 reaction over Pd/La0.9Ba0.1AlO3-delta catalyst at the low temperature of 473 K or below. In a humidified condition, NO reaction with CO on Pd/La0.9Ba0.1AlO3-delta proceeded without being affected by competitive adsorption of NO and CO, whereas that on Pd/Al2O3 was inhibited by strong adsorption of CO on a Pd surface. From in-situ DRIFTS measurements, results showed that nitrite species on the support react with CO adsorbed onto Pd at the periphery of Pd particles and that carbonate species accumulated on Pd/La0.9Ba0.1AlO3-delta are removed rapidly in a humidified condition. Although NO reduction proceeds dominantly on the Pd surface in a dry condition, supplied steam promotes desorption of the surface carbonate to advance the reaction of nitrite with CO for de-NOx in a humidified condition. This mechanism occurs specifically on Pd/La0.9Ba0.1AlO3-delta by virtue of the lattice oxygen and oxygen vacancy on La0.9Ba0.1AlO3-delta.
引用
收藏
页码:192 / 197
页数:6
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