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Phenyl modification of Mn‐containing mesoporous silica and catalytic oxidation of toluene
Author(s) -
Wang Min,
Chen Chen,
Zhang Qiaohong,
Du Zhongtian,
Zhang Zhan,
Gao Jin,
Xu Jie
Publication year - 2010
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.2304
Subject(s) - toluene , catalysis , selectivity , benzoic acid , chemistry , mesoporous silica , surface modification , mesoporous material , catalytic oxidation , contact angle , solvent , chemical engineering , organic chemistry , inorganic chemistry , engineering
BACKGROUND: Catalytic oxidation of toluene with dioxygen is a fundamental industrial technology because the oxidized products are important intermediates for many fine chemicals. In this study, phenyl modification was utilized to alter catalyst surface characteristics in order to enhance activity. RESULTS: Phenyl groups were successfully immobilized on the surface of Mn‐containing hexagonal mesoporous silica (HMS) through a one‐step synthesis route, as demonstrated by detailed characterization. As a result, the surface of the catalyst PhMnHMS was more hydrophobic with a water droplet contact angle of 96°. In the oxidation of toluene to benzoic acid with dioxygen under solvent‐free conditions, this new catalyst showed higher activity and selectivity than non‐organomodified MnHMS, and the conversion and selectivity increased by a factor of 40% and 9%, respectively. CONCLUSION: Modification of the catalyst surface with phenyl groups was an effective strategy to increase activity in the oxidation of toluene. Both conversion and selectivity were improved and this is linked to the hydrophobic character of the surface. This organic modification strategy may also be extended for oxidation of other hydrocarbons. Copyright © 2009 Society of Chemical Industry