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作 者:WEI Bo SUN Jian-min CAO Hui-qun LU Yu-juan FANG Lin
机构地区:[1]Chemistry and Chemical Engineering College, Shenzhen University, Shenzhen 518060, P. R. China [2]State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun 130012, P. R. China
出 处:《Chemical Research in Chinese Universities》2009年第3期286-290,共5页高等学校化学研究(英文版)
基 金:Supported by State Key Laboratory of Inorganic Synthesis and Preparative Chemistry of Jilin University;State Key Laboratory of Physical Chemistry of Solid Surfaces of Xiamen University
摘 要:With alkyl-polyamine triethylene-tetramine as the structure-directing agent, aluminosilicate zeolite ZSM-5(MFI) crystals were synthesized and characterized by XRD, SEM, FTIR, and TG-DTA. The results indicate that the organic amine has a certain influence on the crystal shape and size. The alkaline condition was in favor of the crystallization of ZSM-5 zeolite in the triethylene-tetramine system. The catalytic activity of as-synthesized crystals was examined for the aqueous hydroxylation of phenol with hydrogen peroxide. The phenol conversion was 13.6%, and the selectivities of the as-synthesized samples for catechol, hydroquinone, and benzoquinone were 66.0%, 23.6%, and 10.4%, respectively. The as-synthesized ZSM-5 sample shows a relatively high selectivity towards catechol and could be a promising catalyst.With alkyl-polyamine triethylene-tetramine as the structure-directing agent, aluminosilicate zeolite ZSM-5(MFI) crystals were synthesized and characterized by XRD, SEM, FTIR, and TG-DTA. The results indicate that the organic amine has a certain influence on the crystal shape and size. The alkaline condition was in favor of the crystallization of ZSM-5 zeolite in the triethylene-tetramine system. The catalytic activity of as-synthesized crystals was examined for the aqueous hydroxylation of phenol with hydrogen peroxide. The phenol conversion was 13.6%, and the selectivities of the as-synthesized samples for catechol, hydroquinone, and benzoquinone were 66.0%, 23.6%, and 10.4%, respectively. The as-synthesized ZSM-5 sample shows a relatively high selectivity towards catechol and could be a promising catalyst.
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