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  Highly Ordered Mesoporous Carbon as Catalyst for Oxidative Dehydrogenation of Ethylbenzene to Styrene

Su, D. S., Delgado, J. J., Liu, X., Wang, D., Schlögl, R., Wang, L., et al. (2009). Highly Ordered Mesoporous Carbon as Catalyst for Oxidative Dehydrogenation of Ethylbenzene to Styrene. Chemistry - an Asian Journal, 4, 1108-1113. doi:10.1002/asia.200800424.

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430430_chemasianj_2009.pdf (Preprint), 655KB
 
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 Creators:
Su, Dang Sheng1, Author           
Delgado, Juan Jose1, Author           
Liu, Xi1, Author           
Wang, Di1, Author           
Schlögl, Robert1, Author           
Wang, Lifeng, Author
Zhang, Zhe, Author
Shan, Zhichao, Author
Xiao, Feng-Shou, Author
Affiliations:
1Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              

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Free keywords: dehydrogenation; ethylbeneze; heterogeneous catalysis; mesoporous materials; styrene
 Abstract: We demonstrate that mesoporous carbon without deposition of metal particles is a highly active catalyst. It exhibits both high activity and selectivity in oxidative dehydrogenation of ethylbenzene to styrene, as well as long catalytic stability when compared with activated carbon. Both the as-prepared mesoporous carbon and the active coke formed during the initial stage of the reaction play an important role in the catalytic performance. XPS and IR techniques reveal that the surface oxygen functional groups formed during the reaction are the active sites for the reaction. The ordered mesoporous structure is beneficial for mass transport in catalytic reaction exhibiting long term stability in contrast to activated carbon.

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Language(s): eng - English
 Dates: 2009-05
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 430430
DOI: 10.1002/asia.200800424
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Title: Chemistry - an Asian Journal
  Alternative Title : Chem. Asian J.
Source Genre: Journal
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Pages: - Volume / Issue: 4 Sequence Number: - Start / End Page: 1108 - 1113 Identifier: -