纳米反应器
芳构化
催化作用
沸石
壳体(结构)
反向
化学工程
甲醇
化学
功能(生物学)
材料科学
纳米技术
有机化学
复合材料
几何学
数学
工程类
生物
进化生物学
作者
Ma Qian,Tingjun Fu,Zhuo Wang,Caiyan Li,Xueqing Wu,Ning Yang,Zhong Li
出处
期刊:Small
[Wiley]
日期:2024-01-03
卷期号:20 (24)
被引量:3
标识
DOI:10.1002/smll.202308502
摘要
Abstract Core@shell catalyst composited of dual aluminosilicate zeolite can effectively regulate the distribution of acid sites to control hydrocarbon conversion process for the stable formation of target product. However, the diffusion restriction reduces the accessibility of inner active sites and affects synergy between core and shell. Herein, hollow ZSM‐5 zeolite nanoreactor with inverse aluminum distribution and double shells are prepared and employed for methanol aromatization. It is demonstrated that the intershell cavity alleviated the steric hindrance from zeolites channel and provided more paths and pore entrance for guest molecule. Correspondingly, olefin intermediates generated from methanol over the external shell are easier to adsorb at internal acid sites for further reactions. Importantly, the diffusion of generated aromatic macromolecules to the external surface is also promoted, which slows down the formation of internal coke, and ensures the use of internal acid sites for aromatization. The aromatics selectivity of the nanoreactor remained at 8% after 154 h, while that of solid core@shell catalyst decreased to 2% after 75 h. This finding promises broader insight to improve internal active site utilization of core@shell catalyst at the diffusion level and can be great aid in the flexible design of multifunctional nanoreactors to enhance the relay efficiency.
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