Vapor phase hydroformylation of ethene over Co/SiO 2 promoted by noble metals: dynamic in situ diffuse reflectance FT-IR study of surface species

• Published in: Catalysis today Vol. 20; no. 3; pp. 423 - 435
• Main Authors: Takeuchi, Kazuhiko, Hanaoka, Taka-aki, Matsuzaki, Takehiko, Sugi, Yoshihiro, Ogasawara, Shigeto, Abe, Yoshimoto, Misono, Takahisa
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 1994
• ISSN: 0920-5861; 1873-4308
• DOI: 10.1016/0920-5861(94)80136-3

An in situ diffuse reflectance FT-IR technique was employed to investigate the active surface species and the reaction mechanism of the oxygenate formation in the vapor phase hydroformylation of ethene on Co/SiO 2 promoted with various noble metals such as Ir, Rh, Pt, Re, Ru, and Pd. Co(A)/SiO 2 and Ir(CO)/SiO 2 which were derived from cobalt(II) acetate and Ir 4(CO) 12, respectively, were quite inactive in the reaction, and showed only quite small peaks of adsorbed CO under the conditions of 1.1 MPa of C 2H 4/CO/H 2 at 298 K. In contrast, Co(A)-Ir(CO)/SiO 2, which were very active in the reaction, exhibited strong absorption bands of linear and bridged CO species. At 423–463 K, propanal adsorbed on the catalyst and acyl species which is suggested as the intermediate for the formation of propanal were also observed on this catalyst. By exposing CO preadsorbed on this catalyst to C 2H 4/H 2 at 289 K and 0.1 MPa, the intensity of the linear CO band decreased, and the bands of propanal and acyl species emerged simultaneously, whereas that of the bridged CO band remained constant after the initial drop. These results suggested that the oxygenates are formed via the CO insertion into adsorbed ethyl species, and linear CO species plays a major role in the CO insertion on these noble metal-promoted cobalt catalysts.