催化作用
乙烯
氧化物
X射线光电子能谱
化学
降级(电信)
金属
氧气
环氧乙烷
无机化学
化学工程
有机化学
聚合物
共聚物
工程类
电信
计算机科学
作者
Yufeng Liu,Ying Zhou,Quanli Ke,Mei Lu,Wenxi Zhou,Guokai Cui,Xiaole Weng,Hanfeng Lu
标识
DOI:10.1016/j.apcata.2022.118642
摘要
A thorough catalytic combustion toward diluted ethylene oxide (EO) is demonstrated. The Pt active phase and CeO 2 support were selected to introduce a synergistic effect. As a result, a superior catalytic activity and less severe coking trend were observed on the Pt/CeO 2 catalyst when compared with another widely-used Pt/Al 2 O 3 catalyst. The XPS spectra and H 2 -TPR profiles evidenced that the Pt/CeO 2 catalyst has both stronger metal-support interaction and more abundant oxygen vacancies, which is believed at the heart of its excellent performance. Finally, the degradation pathways of EO were explored by in-situ DRIFTS. The weak H 2 O affinity of Pt/CeO 2 catalyst can inhibit the polycondensation reaction and result in the favorable degradation of EO. In contrast, abundant hydroxyl species were present on the hydrophilic Pt/Al 2 O 3 catalyst surface, which may serve as acid sites and complicate the EO degradation, and therefore various side products and carbon deposits would appear in this case. • Extremely diluted EO is fully oxidized on Pt/CeO 2 catalyst under low temperature • Metal-support interaction & oxygen vacancy abundance are proved the key to activity • Pt/CeO 2 shows both superior catalytic activity and anti-coking property to Pt/Al 2 O 3 • The different degradation pathways of two catalysts are elucidated by in situ DRIFTs
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