Issue 5, 1989

Infrared study of the adsorption of ethanoic acid, acrylic acid, acetone, acrolein and propene–NO mixtures on Rh/SiO2 catalysts

Abstract

Infrared spectra of the adsorbed products of reaction of propene and NO over Rh/SiO2 are compared with spectra of adsorbed acetone, acrolein, acrylic acid and ethanoic acid. Acetone and acrolein formed hydrogen bonds with surface silanol groups and underwent decomposition on rhodium to give rhodium carbonyl species. The carboxylic acids also gave rhodium carbonyl species, but for ethanoic acid this only occurred at high temperature. Both acids were adsorbed on silica either through chemisorption giving a surface ester or as a weakly held dimer. Heat treatment of Rh/SiO2 in propene/NO mixtures gave acrylic acid as the dominant partial oxidation product. However, addition of propene before NO to the reaction system led to the generation of a surface poison which inhibited the oxidation of propene.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans. 1, 1989,85, 1129-1138

Infrared study of the adsorption of ethanoic acid, acrylic acid, acetone, acrolein and propene–NO mixtures on Rh/SiO2 catalysts

J. A. Anderson and C. H. Rochester, J. Chem. Soc., Faraday Trans. 1, 1989, 85, 1129 DOI: 10.1039/F19898501129

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements