Styrene from toluene by side chain alkylation over a novel solid acid-base catalyst
[Display omitted] • A novel solid acid-base catalyst containing N and Al atoms has been synthesized successfully. • Styrene yield (44.9%) and selectivity (97.6%) can be achieved for side chain alkylation of toluene with methanol over the catalyst. • For side chain alkylation of toluene, three crucia...
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Published in | Catalysis today Vol. 173; no. 1; pp. 38 - 43 |
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Main Authors | , , , , , |
Format | Journal Article Conference Proceeding |
Language | English |
Published |
Amsterdam
Elsevier B.V
01.09.2011
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | [Display omitted]
• A novel solid acid-base catalyst containing N and Al atoms has been synthesized successfully. • Styrene yield (44.9%) and selectivity (97.6%) can be achieved for side chain alkylation of toluene with methanol over the catalyst. • For side chain alkylation of toluene, three crucial parameters of catalyst are the weak and/or middle acid sites, middle base sites and the befitting distance between acid and base sites.
A novel solid acid-base catalyst with aluminum and nitrogen were prepared from aluminum and amine by using triblock copolymer Pluronic F127 as a template and resol as framework via evaporation induced organic–organic assembly method. The catalyst was characterized by UV–vis absorption spectra (UV–vis), fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectra (XPS), the acid-base properties of the catalyst were determined by temperature programmed desorption (TPD) using CO
2 and NH
3 as probe molecules, and the side chain alkylation of toluene with methanol over the catalyst has been investigated. The results show that Cat–NH(C
2H
5)
2 demonstrates the higher activity and selectivity, styrene yield reaches 44.9% and selectivity 97.6%. It is considered that the strength of base and distance of the specific surface acid-base pairs over the catalysts are favored to bimolecular side-chain alkylation reaction. |
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Bibliography: | http://dx.doi.org/10.1016/j.cattod.2011.05.038 |
ISSN: | 0920-5861 1873-4308 |
DOI: | 10.1016/j.cattod.2011.05.038 |