Liquid phase hydrogenation of cinnamaldehyde on Cu-based catalysts

ALBERTO MARCHI; DIEGO GORDO; ANDRÉS TRASARTI; CARLOS APESTEGUÍA

APPLIED CATALYSIS A-GENERAL

Elsevier

Lugar: Amsterdam; Año: 2003 vol. 249 p. 53 - 67

0926-860X

The liquid phase hydrogenation of cinnamaldehyde was studied at 393 K and 10 bar on Cu-based catalysts containing about 12 wt.% of copper. Cu/SiO2 was prepared by incipient wetness impregnation while Cu-Al, Cu-Zn-Al, and Cu-Ni(Co)-Zn-Al catalysts were obtained by coprecipitation at constant pH. Cinnamaldehyde was initially hydrogenated to cinnamyl alcohol and hydrocinnamaldehyde, and these products consecutively yielded hydrocinnamyl alcohol. Hydrogenation kinetic constants were determined by modelling catalytic data and using a pseudohomogeneous kinetic network. The reaction occurred via two different pathways depending on the composition and surface properties of the catalyst. On Cu/SiO2 and binary Cu-Al samples, cinnamaldehyde hydrogenation proceeded via a monofunctional pathway on metallic copper that produced predominantly hydrocinnamaldehyde. Ternary Cu-Zn-Al and quaternary Cu-Ni(Co)-Zn catalysts were about one order of magnitude more active than Cu/SiO2 for cinnamaldehyde conversion and produced predominantly cinnamyl alcohol. The general composition formula of reduced Cu-Zn-Al and Co-Ni(Co)-Zn-Al catalysts was Cu00,5·[MO]0,5·ZnAl2O4, where M is Zn, Co, or Ni. These catalysts contained the Cu0 particles highly dispersed in a super-stoichometric zinc aluminate spinel and in close interaction with M+2 cations. The presence of M+2 cations provided a new reaction pathway for adsorbing and hydrogenating cinnamaldehyde in addition to the metal copper active sites. Cinnamaldehyde interacts linearly via the C=O group with M+2 sites and is selectively hydrogenated o unsaturated alcohol by atomic hydrogen activated in neighboring Cu0 sites. Formation of surface Cu0-M+2 sites was, therefore crucial to efficiently catalyze the cinnamyl alcohol formation from cinnamaldehyde via a dual-site reaction pathway.