Hydrogenation of crotonaldehyde and butyraldehyde on

MERLO, ANDREA; GERARDO SANTORI; SAMBETH, JORGE; SIRI, GUILLERMO; CASELLA MÓNICA; FERRETTI, OSMAR

CATALYSIS COMMUNICATIONS

Elsevier

Lugar: Amsterdam; Año: 2006 vol. 7 p. 204 - 208

1566-7367

Abstract A DRIFTS ‘‘in situ’’ study on Pt and PtSn catalysts used in the crotonaldehyde and butyraldehyde hydrogenation was carried out in this work. Results show that, on Pt/SiO2 catalyst a decarbonylation process takes place during the initial reaction minutes, causing an instantaneous and irreversible deactivation. The tin addition improves the stability of the resulting catalyst due to the inhibition of CO formation. Bands assigned to the presence of superficial olefinic species allow to explain the deactivation observed, which is more important in the case of butyraldehyde hydrogenation. In the crotonaldehyde hydrogenation with PtSn/SiO2 catalyst, the band at 1651 cm1 is assigned to C@O strongly coordinated, explaining the high selectivity to UOL of this catalytic system.2 catalyst a decarbonylation process takes place during the initial reaction minutes, causing an instantaneous and irreversible deactivation. The tin addition improves the stability of the resulting catalyst due to the inhibition of CO formation. Bands assigned to the presence of superficial olefinic species allow to explain the deactivation observed, which is more important in the case of butyraldehyde hydrogenation. In the crotonaldehyde hydrogenation with PtSn/SiO2 catalyst, the band at 1651 cm1 is assigned to C@O strongly coordinated, explaining the high selectivity to UOL of this catalytic system.