Combining trace Pt with surface silylation to boost Au/uncalcined TS-1 catalyzed propylene epoxidation with H2 and O2

被引:11
|
作者
Wang, Gang [1 ]
Du, Wei [1 ]
Zhang, Zhihua [1 ]
Tang, Yanqiang [1 ]
Xu, Jialun [1 ]
Cao, Yueqiang [1 ]
Qian, Gang [1 ]
Duan, Xuezhi [1 ]
Yuan, Weikang [1 ]
Zhou, Xinggui [1 ]
机构
[1] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
Au-Pt; TS-1; catalyst; propylene epoxidation; propylene oxide production; silylation promotion; triple Au-Pt-Ti active sites; GAS-PHASE EPOXIDATION; PROPENE EPOXIDATION; GOLD NANOPARTICLES; DEPENDENT ACTIVITY; ACTIVE-SITES; OXIDE; PERFORMANCE; STABILITY; AU/TS-1; AU/TIO2;
D O I
10.1002/aic.17416
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Modification of bifunctional Au-Ti catalysts for direct epoxidation of propylene with H-2 and O-2 is of burgeoning interest for potential commercialization requirements with desirable overall catalytic performance. Herein, we report a strategy by combining the addition of trace Pt into Au particles to enhance hydroperoxide species formation with the surface silylation to promote propylene oxide (PO) desorption. The resultant catalyst, that is, silylated Au20Pt1/uncalcined TS-1, gives rise to significantly enhanced propylene conversion of 11%, PO selectivity of 88%, and H-2 efficiency of 41%. The underlying nature of the above enhanced performance is elucidated by multiple techniques, such as high-angle annular dark-field scanning transmission electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectra, and theoretical calculations. The insights revealed here, the synergy of Au-Pt-Ti triple active sites together with the surface silylation, could guide the rational design of Au-Ti catalysts for propylene epoxidation to boost PO production.
引用
收藏
页数:9
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