期刊
NATURE CATALYSIS
卷 1, 期 7, 页码 547-554出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/s41929-018-0104-7
关键词
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资金
- European Union [ERC-AdG-2014-671093]
- Spanish Government-MINECO through Severo Ochoa [SEV-2016-0683, MAT2015-71261-R]
- China Scholarship Council
Catalysis with enzymes and zeolites have in common the presence of well-defined single active sites and pockets/cavities where the reaction transition states can be stabilized by longer-range interactions. We show here that for a complex reaction, such as the conversion of methanol-to-olefins (MTO), it is possible to synthesize reaction-adapted zeolites by using mimics of the key molecular species involved in the MTO mechanism. Effort has focused on the intermediates of the paring mechanism because the paring is less favoured energetically than the side-chain route. All the organic structure-directing agents based on intermediate mimics crystallize cage-based small-pore zeolitic materials, all of them capable of performing the MTO reaction. Among the zeolites obtained, RTH favours the whole reaction steps following the paring route and gives the highest propylene/ethylene ratio compared to traditional CHA-related zeolites (3.07 and 0.86, respectively).
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