化学
沸石
苯乙烯
分区
反向
化学工程
催化作用
有机化学
共聚物
几何学
工程类
聚合物
数学
政治学
法学
作者
Zhe Hong,Lihua Deng,Fanglin Wang,Fangyu Zhu,Yingsen Fang,Li Song,Lei Li,Zhirong Zhu
标识
DOI:10.1021/acs.inorgchem.4c03697
摘要
ZSM-5 zeolites with accessible micropore architecture and tunable acid-base sites are important shape-selective catalysts. However, the presence of exposed straight channels and the external acid-base sites of conventional ZSM-5 has a negative impact on shape selectivity. Herein, we report on the direct synthesis of an intergrowth ZSM-5 zeolite mimicking the mortise-tenon joints. It can be revealed by various methods that the mortise-tenon ZSM-5 shows an inverse Al gradient from the surface to the core of the zeolite. More importantly, the sinusoidal channels predominantly opened to their external surfaces are constructed. The shape-selective capability of the ZSM-5 zeolite has been fully exploited due to the intrinsic inert external surface and unique sinusoidal channel features, thereby resulting in high styrene selectivity (>90%) and good catalytic stability (>100 h) in the toluene side-chain alkylation reaction. In addition, in situ DRIFTS confirms that this intergrowth ZSM-5 contributes to the formation of more active intermediates of HCOO* and H
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