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Catalytic Ketonisation over Oxide Catalysts. Part VII. Ketonisation and Cross-Ketonisation of Aliphatic Esters over CeO2 and ZrO2 Supported on Alumina

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Catalysts of general formula xwt% MO2/Al2O3, where x = 10, 20 or 30 and M = Ce or Zr have been studied in the ketonisation and cross-ketonisation of aliphatic esters under flow conditions between 548-723 K. Ketonisation of ethyl pentanoate, heptanoate and nonanoate has led to nonan-5-one, tridecan-7-one and heptadecan-9-one, respectively. The conversion of esters increased with temperature and at 698 K a quantitative conversion was observed, irrespective of the type of ester used. A maximum yield of ketone (46% for nonan-5-one, 60% for tridecan-7-one and 50% for heptadecan-9-one) was observed at 673 K. As a result of the cross-ketonisation of a mixture of ethyl pentanoate and ethyl nonanoate (3:1 molar ratio), three ketones were formed: nonan-5- one, tridecan-5-one and heptadecan-9-one. At 698 K, maximum yields of ketones were noted (37, 46 and 8%, respectively) together with a 90% conversion of esters. The catalysts were characterized by XRD, TPR and surface area measurements.
Rocznik
Strony
1033--1038
Opis fizyczny
Bibliogr. 12 poz., rys.
Twórcy
autor
  • Faculty of Chemistry, Warsaw University of Technology (Politechnika), Laboratory of Catalytic Synthesis, Noakowskiego 3, 00-664 Warsaw, Poland
  • Faculty of Chemistry, Warsaw University of Technology (Politechnika), Laboratory of Catalytic Synthesis, Noakowskiego 3, 00-664 Warsaw, Poland
autor
  • Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland
Bibliografia
  • 1. Squibb E. J. Am. Chem. Soc., 17, 187 (1895).
  • 2. Swann S., Appel E. G. and Kistler S.S., Ind. Eng. Chem., 26, 1014 (1934).
  • 3. Gliński M. and Kaszubski M., React. Kinet. Catal. Lett., 70, 271 (2001).
  • 4. Gliński M. and Kaszubski M„ Polish J. Chem., 76, 1037 (2002).
  • 5. Gliński M. and Szudybill J., React. Kinet. Catal. Lett., 77, 335 (2002).
  • 6. Gliński M. Kijeński J. and Jakubowski A., Appl. Catal. A: General, 128, 209 (1995).
  • 7. Gliński M. and Kijeński J., Appl. Catal. A: General, 190, 87 (2000).
  • 8. Gliński M., Szymański W. and Łomot D., Appl. Catal. A: General, (in preparation).
  • 9. Hernandez A., Ruette R and Ludena E.V., J. Mol. Catal., 39, 21 (1987).
  • 10. Yamaguchi T., Ikeda N., Hattori H. and Tanabe K,,J. Catal., 67, 324 (1981).
  • 11. Laachir A., Perrichon V., Badri A., Lamotte J., Catherine E., Lavalley J-C., El Fallah J., Hilaire L., le Normand F.,QuemereE.,Sauvion G-N. and Touret O., J.Chem. Soc. Farad. Trans., 81, 1601 (1991).
  • 12. Zotin F., Toumayan L., Varloud J., Perrichon V. and Frety R., Appl. Catal. A: General, 78, 31 (1991).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0021-0068
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