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Gemini‐type cationic surfactant‐directed synthesis of hollow ZSM‐5 zeolite with intracrystalline mesopores and its application in the hydroxylation of phenol
Author(s) -
Shen Yu,
Wang Fumin,
Han Zongzhuang,
Zhang Xubin
Publication year - 2018
Publication title -
journal of chemical technology and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.64
H-Index - 117
eISSN - 1097-4660
pISSN - 0268-2575
DOI - 10.1002/jctb.5501
Subject(s) - zeolite , mesoporous material , catalysis , hydroxylation , phenol , cationic polymerization , chemistry , zsm 5 , chemical engineering , selectivity , hydrothermal circulation , inorganic chemistry , organic chemistry , engineering , enzyme
Abstract BACKGROUND ZSM‐5 zeolites are of great importance in industrial catalysis. However, the diffusion limitations caused by small pore opening restrict the extent of catalytic conversions over conventional ZSM‐5. Many studies have shown that mass transfer in zeolite channels can be improved by controlling the morphology or creating additional mesoporosity. Here, the catalytic performance is further improved by the creation of hollow structure and intracrystalline mesopores in ZSM‐5 zeolite. RESULTS The characterization results demonstrated that hollow ZSM‐5 with intracrystalline mesopores can be synthesized by using a simple one‐step hydrothermal strategy with a commercial gemini‐type cationic surfactant containing hydrophilic hydroxyl groups. Compared with the Fe‐substituted conventional ZSM‐5, the Fe‐substituted hollow ZSM‐5 with intracrystalline mesopores show remarkably enhanced catalytic performance in the hydroxylation of phenol. About 52.2% conversion of phenol can be obtained with almost 96.8% selectivity to dihydroxybenzenes. The catalytic activity remained almost unchanged after five cycles. CONCLUSION The newly created hollow structure and intracrystalline mesopores in ZSM‐5 zeolite showed enhanced catalytic activity and reusability for the hydroxylation of phenol, which is higher than most reported systems. The prepared catalyst is a promising alternative material for the hydroxylation of phenol. © 2017 Society of Chemical Industry