The hydrogenation of citral and cinnamaldehyde has been investigated over Ru/Al2O3 catalysts. The effect of metal partick size on the catalytic activity and selectivity has been studied by using catalysts having a metal dispersion ranging from 0.05 to 0.88. It has been observed that the overall rate of hydrogenation of both the unsaturated aldehydes is not influenced by the Ru particle size. In the hydrogenation of cinnamaldehyde a higher selectivity to cinnamyl alcohol has been observed on catalysts with larger metal particle size. No variations have been found in the hydrogenation of citral. It is suggested that steric effects do not influence significantly the product selectivity. A repulsive interaction between the aromatic ring and the catalyst surface would explain the higher selectivity to cinnamyl alcohol. On ail the investigated catalysts the isolated C=C double bond of citral shows a low reactivity. It is suggested th;rt the unsaturated aldehyde is adsorbed through the carbonyl group. This strong adsorption prevents !he hvdlogenatioa of the kllated oleEnic bond which is located far away fron, the adsorption centers.
Hydrogenation of (a,b-unsaturated aldehydes over Ru/Al2O3 catalysts
DONATO, Andrea
1996-01-01
Abstract
The hydrogenation of citral and cinnamaldehyde has been investigated over Ru/Al2O3 catalysts. The effect of metal partick size on the catalytic activity and selectivity has been studied by using catalysts having a metal dispersion ranging from 0.05 to 0.88. It has been observed that the overall rate of hydrogenation of both the unsaturated aldehydes is not influenced by the Ru particle size. In the hydrogenation of cinnamaldehyde a higher selectivity to cinnamyl alcohol has been observed on catalysts with larger metal particle size. No variations have been found in the hydrogenation of citral. It is suggested that steric effects do not influence significantly the product selectivity. A repulsive interaction between the aromatic ring and the catalyst surface would explain the higher selectivity to cinnamyl alcohol. On ail the investigated catalysts the isolated C=C double bond of citral shows a low reactivity. It is suggested th;rt the unsaturated aldehyde is adsorbed through the carbonyl group. This strong adsorption prevents !he hvdlogenatioa of the kllated oleEnic bond which is located far away fron, the adsorption centers.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
