Autocatalytic induction period in zeolite-catalyzed methanol conversion

被引:6
|
作者
Lin, Shanfan [1 ,3 ]
Wei, Yingxu [1 ]
Liu, Zhongmin [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, IChEM Collaborat Innovat Ctr Chem Energy Mat, Natl Engn Res Ctr Lowercarbon Catalysis Technol,Da, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[3] Univ Chinese Acad Sci, Energy Coll, Beijing 100049, Peoples R China
来源
CHEM CATALYSIS | 2023年 / 3卷 / 05期
基金
中国国家自然科学基金;
关键词
CARBON-CARBON BOND; TO-HYDROCARBONS; DIMETHYL ETHER; REACTION-MECHANISM; HYDROGEN-TRANSFER; CO-REACTION; OLEFINS; H-ZSM-5; WATER; EVOLUTION;
D O I
10.1016/j.checat.2023.100597
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The autocatalytic induction period is the key feature of zeolite-catalyzed methanol conversion. Associated with the generation of the initial C-C bond, it has been an attractive topic of intense debate in the field of C1 chemistry for decades. While an in-depth understanding of the induction period of methanol conversion has not been achieved, in recent years, a host of works have emerged that provide new insight into the origination of the initial C-C bond, especially from the point of view of the activation of C1 species. Particularly, full-spectrum molecular routes of methanol conversion have been established, and the effects of in situ-produced H2O and zeolite local microenvironments have received increasing attention. In these contexts, this perspective condenses our critical view on the autocatalytic induction period of methanol conversion and highlights the challenges and opportunities of the local microenvironments under real working conditions for uncovering the complex reaction mechanism of zeolite catalysis.
引用
收藏
页数:13
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