化学
沸石
介孔材料
微型多孔材料
结晶度
高分辨率透射电子显微镜
分子筛
催化作用
水热合成
无机化学
结晶
化学工程
选区衍射
核化学
热液循环
有机化学
结晶学
透射电子显微镜
工程类
作者
Shiyao Wang,Ziliang Zheng,Bo He,Chen Sun,Xing Li,Xu Wu,Xia An,Xianmei Xie
摘要
Novel hierarchical Beta zeolites have been successfully synthesized via a one‐pot dual‐templates strategy utilizing gemini organic surfactant and tetraethylammonium hydroxide (TEAOH)through hydrothermal process. The influence of several parameters on the formation of hierarchical Beta zeolite, the change in acidity and a possible growth scheme were systematically investigated. The physicochemical properties of these catalysts were characterized by PXRD, BET, SEM, HRTEM SAED, TG and NH 3 ‐TPD techniques, and the performance as acid catalysts was verified using the transformation of EtOH as a model reaction. On one hand, WAXRD data indicated that decreasing the temperature of synthesis and increasing amounts of C 12‐6‐12 in the process of synthesis resulted in lower crystallinity of Beta zeolites due to the BEA nuclei formation and crystal growth constrained by C 12‐6‐12 . On the other hand, SAXRD and HRTEM data evidenced that C 12‐6‐12 initially generated a pseudo‐ordered mesoporous phase which was then partially occupied by the zeolite. After a period of ~96 h for crystallization, the hierarchy zeolite possessing 765.7 m 2 ·g ‐1 of Brunauer‐Emmett‐Tellerarea, and average mesopore size distribution of 3.51 nm can be synthesized, and its microporous structure has a good crystallinity and lower amounts of acid sites than that of the microporous Beta one. Furthermore, the as‐obtained hierarchical zeolite displayed lower deactivation rate mainly due to the less coke formation on the surface of catalyst. It is expected to develop more considerable potential application value for the hierarchical Beta zeolite structure in the near future.
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