Liquid phase aldol condensation of cyclopentanone with valeraldehyde catalysed by oxynitrides possessing tuneable acid-base properties

Hasni, Moez;Prado, G;Rouchaud, Jean;Grange, Paul;Delsarte, Stéphanie;et.al.
(2006) Journal of Molecular Catalysis A: Chemical — Vol. 247, n° 1-2, p. 116-123 (2006)

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Authors
  • Hasni, MoezUCLouvain
    Author
  • Prado, G
    Author
  • Rouchaud, JeanUCLouvain
    Author
  • Grange, PaulUCLouvain
    Author
  • Devillers, Michelorcid-logoUCLouvain
    Author
  • Delsarte, StéphanieUCLouvain
    Author
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Abstract
The aldol condensation reaction between valeraldehyde and cyclopentanone was carried out in a batch reactor, at atmospheric pressure and 130 degrees C over "AIPON" and "ZrPON" catalysts. Those catalysts were obtained by heating AlPO4 and Zr0.9PO4.3 phosphates in a flow of gaseous ammonia at 750 and 700 degrees C, respectively. The nitridation treatment allows to substitute framework oxygen atoms by nitrogen atoms, consequently reducing the number of solid acid sites and increasing the number of basic sites. Nitridation has a positive effect on valeraldehyde conversion which increases from 33 to 57% after 2h of reaction for the "AIPO" system and from 80 to 94% after 2h for the "ZrPO" system. The influence of the acid-base properties of catalysts for this particular reaction is discussed by measuring the activity and selectivity of basic (MgO), and amphoteric (Al2O3) catalysts. The zirconophosphate precursor "ZrPO" and its nitrided samples are the most active for the reaction. (c) 2005 Elsevier B.V. All rights reserved.
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Citations

Hasni, M., Prado, G., Rouchaud, J., Grange, P., Devillers, M., & Delsarte, S. (2006). Liquid phase aldol condensation of cyclopentanone with valeraldehyde catalysed by oxynitrides possessing tuneable acid-base properties. Journal of Molecular Catalysis A: Chemical, 247(1-2), 116-123. https://doi.org/10.1016/j.molcata.2005.11.023 (Original work published 2006)