催化作用
初湿浸渍
分解
解吸
扫描电子显微镜
透射电子显微镜
钌
分析化学(期刊)
材料科学
金属
核化学
化学
无机化学
物理化学
纳米技术
吸附
选择性
冶金
色谱法
有机化学
复合材料
作者
Takeshi Furusawa,Hiroki Kuribara,Koji Kimura,Takafumi Sato,Naotsugu Itoh
标识
DOI:10.1021/acs.iecr.0c03112
摘要
Cl-free Ru/CeO2 spherical catalysts were prepared by incipient wetness impregnation and subsequent washing processes using RuCl3·3H2O and a commercial spherical CeO2 support. Cs addition improved the catalytic performance for NH3 decomposition, and the optimal Cs loading was a Cs/Ru molar ratio of 0.43. Transmission electron microscopy (TEM) and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM–EDX) suggested that Cs was present around Ru metal particles and served as an anchor for forming small, well-dispersed Ru metal particles (∼2 nm). CO2 temperature-programmed desorption results indicated that the Cs-Ru/CeO2 catalyst had more strong basic sites than the Ru/CeO2 catalyst. Kinetic analysis results clearly demonstrated that Cs addition promoted recombinative desorption of N atoms, which is the rate-determining step of NH3 decomposition. Consequently, the Cs-Ru/CeO2 spherical catalyst (Cs/Ru = 0.43) treated in Ar for 1 h at 773 K exhibited high catalytic activity for NH3 decomposition (NH3 conversion: 40% at 523 K and 80% at 573 K) at 2000 mL-NH3 g cat–1 h–1.
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