Enhanced catalytic oxidation of diluted ethylene oxide on Pt/CeO2 catalyst under low temperature

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
出处
期刊:Applied Catalysis A-general [Elsevier BV]
卷期号:639: 118642-118642 被引量:9
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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