脱氢
丙烷
催化作用
材料科学
化学工程
化学
业务
有机化学
工程类
作者
Kai Wu,Vita A. Kondratenko,Mingxia Zhou,Dmitry E. Doronkin,Stephan Bartling,Qiyang Zhang,Shanlei Han,Xin Jia,Qi Liu,Dong Xiong,Chunming Xu,Guiyuan Jiang,Dan Zhao,Uwe Rodemerck,David Linke,Evgenii V. Kondratenko
标识
DOI:10.1002/anie.202506704
摘要
Abstract Although PtGaO x ‐containing catalysts are active and selective in the non‐oxidative dehydrogenation of propane (PDH) to propylene, they suffer from rapid deactivation and, especially, inability to recover their initial performance in a series of PDH/oxidative regeneration cycles, characteristics that are highly relevant to commercialization. Herein, we identified reducibility of GaO x as the key descriptor affecting the above catalyst features. Oxidized GaO x species are more active than reduced GaO x in the recombination of two H species formed from propane, which is the rate‐limiting step in the PDH reaction. This process is further accelerated by Pt. The reduction of GaO x with time on propane stream leads to catalyst deactivation. Easily reducible GaO x also tend to form PtGaO x under PDH conditions, from which Pt atoms present in fresh catalysts cannot be completely recovered during oxidative regeneration, which is detrimental to catalyst durability. Regardless of the reaction atmosphere, Pt single atoms exist on the surface of PtGaO x ‐containing catalysts with hardly reducible GaO x . Based on the knowledge derived, we developed a catalyst with 500 ppm Pt on the surface of mixed GaAlO x , which outperforms almost all previous PtGaO x ‐containing catalysts in terms of space‐time yield of propylene formation and shows durable operation under industrially relevant conditions.
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