沸石
介孔材料
微型多孔材料
化学工程
热液循环
材料科学
催化作用
催化裂化
分子筛
大孔隙
纳米技术
化学
有机化学
复合材料
工程类
作者
Xinyu Li,Jose Andres Hernandez Gaitan,Shinya Kokuryo,Tomoka Sumi,Haruna Kitamura,Koji Miyake,Yoshiaki Uchida,Norikazu Nishiyama
标识
DOI:10.1016/j.micromeso.2022.112096
摘要
Zeolites have been served as multifunctional microporous materials. However, diffusion limitation often exists within zeolitic micropores, limiting their performances. Hierarchical zeolites with meso- or macropores have been synthesized by an effective approach to solving the above problem. Herein, we synthesized hierarchical zeolites via an alkaline treatment for organic structure-directing agents (OSDA)-occluded zeolites. In this method, desilication occurred only on the external surfaces of zeolites thanks to the presence of OSDA, leading to selective formation of mesopores only on the external surfaces of zeolites. The zeolite with mesopores only on external surfaces showed much higher catalytic activity on cracking of low-density polyethylene than a pristine zeolite. The catalytic performance was the same as a conventional hierarchical zeolite with mesopores in overall particles. These results demonstrated that mesopores on the external surfaces of zeolites played important roles in improving mass transfers of the reactants. In addition, the zeolites with mesopores only on the external surfaces showed higher hydrothermal stability than the conventional hierarchical zeolite due to its fewer defects consisting of SiOH or AlOH. This work presented a new strategy for controlling the pore structures of zeolites.
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