钌
催化作用
分解
沸石
无机化学
化学
氢
铈
氨
金属
吸附
物理化学
有机化学
作者
Keiji Hashimoto,Naoji Toukai
出处
期刊:Journal of Molecular Catalysis A-chemical
[Elsevier]
日期:2000-11-01
卷期号:161 (1-2): 171-178
被引量:67
标识
DOI:10.1016/s1381-1169(00)00332-0
摘要
Ammonia decomposition proceeds at 300°C over a catalyst consisting of ruthenium metal and CeO2 highly dispersed on Y-form zeolite. The catalyst, Ru-CeO2/YZ, is highly active for NH3 decomposition under conditions at which Y-form zeolite and CeO2 do not work. The decomposition rate is first order in ammonia. The initial rate of nitrogen adsorption supports the decomposition mechanism involving a rate-limiting step in dinitrogen desorption. Moreover, the load of ruthenium particles on CeO2/YZ catalyst makes an inhibition of the decomposition rate by hydrogen less strong. IR spectra for the catalyst indicate that the ammonia decomposition proceeds via the formation of the intermediate species, such as RuNH3, RuNH2, RuN2 and RuH on the surface of ruthenium. The adsorption of hydrogen and XRD data support the idea that ruthenium is highly dispersed in the Ru-CeO2/YZ
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