The Isomerization of Propylene Oxide on Metal Phosphate Catalysts
- 1 May 1972
- journal article
- research article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 45 (5) , 1353-1357
- https://doi.org/10.1246/bcsj.45.1353
Abstract
The isomerization of propylene oxide was carried out on metal phosphate catalysts. The main products were allyl alcohol, propionaldehyde, acetone, and 1-propanol. It was found that allyl alcohol is produced by acid-base bifunctional catalysts, acetone, by basic-site catalysts only, and propionaldehyde, by acid-site catalysts. 1-Propanol may be produced by the hydrogen-transfer reaction of allyl alcohol. The conversion to propionaldehyde is proportional to the acidity of the catalyst, the strength of which is stronger than H0=+4.8. The sum of the conversions to allyl alcohol, acetone, and 1-propanol correlate linearly with the observed basicity (H0≥+7.2) of the catalyst. The selectivity and activity are determined by the basic and acidic properties of the catalyst. The mechanisms of the propylene oxide isomerization are also discussed.Keywords
This publication has 6 references indexed in Scilit:
- Dehydration and Dehydrogenation of Alcohols over Acid-Base Bifunctional CatalystsBulletin of the Chemical Society of Japan, 1971
- Calcium-oxide-catalyzed reactions of hydrocarbons and of alcoholsJournal of Catalysis, 1968
- The catalytic activity and selectivity of unsupported metal sulfates for the isomerization of n-butenesJournal of Catalysis, 1968
- The catalytic activity and selectivity of metal sulfates for the isomerization of n-butenesJournal of Catalysis, 1967
- ThietanesChemical Reviews, 1966
- ThiiranesChemical Reviews, 1966