环氧丙烷
催化作用
化学
溶剂分解
沸石
无机化学
丙烯
过氧化氢
选择性
过氧化物
化学工程
有机化学
水解
环氧乙烷
聚合物
共聚物
工程类
作者
Kang Tang,Weilong Hou,Xiaoshu Wang,Wen Xu,Xinqing Lu,Rui Ma,Yanghe Fu,Weidong Zhu
标识
DOI:10.1016/j.micromeso.2021.111492
摘要
The titanosilicate zeolite catalyzed epoxidation of propylene with hydrogen peroxide (H2O2, HP) to propylene oxide (PO), the so-called HPPO, is more eco-efficient, compared to the chlorohydrin process and the epoxidation using organic hydroperoxides. However, the zeolite catalysts used in the HPPO process are easily deactivated, because the main byproduct propylene glycol (PG) and other heavy byproducts with high boiling points, derived from the solvolysis of PO, are deposited inside the zeolite micropores. In the present work, trimethylsilylated Ti-MWW zeolites, named Si–Ti-MWW, were developed for the HPPO process. In combination with the results from extensive characterizations for the prepared zeolites, it is found that the trimethylsilylation merely occurs on the external surface of Ti-MWW crystals and can significantly enhance the hydrophobicity, but not alter the coordination states of the Ti species and textural properties of the zeolites. The catalytic properties of Ti-MWW and Si–Ti-MWW were compared in propylene epoxidation. The results show that the solvolysis of PO to the byproducts can be effectively inhibited over the hydrophobic zeolite surface, making Si–Ti-MWW exhibit a much higher selectivity for PO and a much better stability and reusability than the parent Ti-MWW in the HPPO process. The current study, therefore, provides a new approach to develop efficient catalysts for the HPPO process.
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