Elsevier

Journal of Catalysis

Volume 181, Issue 2, 25 January 1999, Pages 217-222
Journal of Catalysis

Regular Article
Addition of Carboxylic Acids to Cyclic Olefins Catalyzed by Strong Acidic Ion-Exchange Resins

https://doi.org/10.1006/jcat.1998.2300Get rights and content

Abstract

The esterification of several cyclic olefins with saturated and unsaturated carboxylic acids has been studied over highly dispersed strongly acidic ion-exchange resins based on Nafion, where the Nafion is entrapped within a porous silica matrix. Over these new catalysts the accessibility of the acid sites is much improved, in comparison to the original material. The activity has been compared to that of Amberlyst 15. The Nafion-based catalyst materials are superior to the weaker acidity Amberlyst catalysts when less active olefins are used and especially at low temperatures.

References (15)

  • Q. Sun et al.

    J. Catal.

    (1996)
  • A. Heidekum et al.

    J. Catal.

    (1998)
  • A. Chakrabarti et al.

    React. Polym.

    (1993)
  • Riondel, A. Feb. 26,...
  • Gude, F. Bellut, H. July 18,...
  • Sandoz-Patent-GmbH, July 1,...
  • H.A. Bruson et al.

    J. Am. Chem. Soc.

    (1945)
There are more references available in the full text version of this article.

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To whom correspondence should be addressed. E-mail: hoelderich@ rwth-aachen.de.

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