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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received October 19, 2010
Accepted November 22, 2010
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Catalytic decomposition of benzyl phenyl ether to aromatics over cesium-exchanged heteropolyacid catalyst

School of Chemical and Biological Engineering, Institute of Chemical Processes, Seoul National University, Shinlim-dong, Gwanak-gu, Seoul 151-744, Korea
inksong@snu.ac.kr
Korean Journal of Chemical Engineering, May 2011, 28(5), 1177-1180(4), 10.1007/s11814-010-0491-1
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Abstract

Cesium-exchanged CsxH3.0-xPW12O40 (X=2.0-3.0) heteropolyacid catalysts were prepared and applied to the decomposition of benzyl phenyl ether to aromatics. Benzyl phenyl ether was chosen as a lignin model compound for representing α-O-4 bond in lignin. Phenol, benzene, and toluene were mainly produced by the decomposition of benzyl phenyl ether. Conversion of benzyl phenyl ether and total yield for main products (phenol, benzene, and toluene) were closely related to the surface acidity of CsxH3.0-xPW12O40 (X=2.0-3.0) heteropolyacid catalyst. Conversion of benzyl phenyl ether and total yield for main products increased with increasing surface acidity of the catalyst. Among the catalysts tested, Cs2.5H0.5PW12O40 with the largest surface acidity showed the highest conversion of benzyl phenyl ether and total yield for main products.

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