TY - JOUR
T1 - In-Situ generation of surface-active HCo(CO)y like intermediate from gold supported on ion-promoted Co3O4 for induced hydroformylation-hydrogenation of alkenes to alcohols
AU - Oseghale, Charles O.
AU - Mogudi, Batsile M.
AU - Akinnawo, Christianah A.
AU - Meijboom, Reinout
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2020/7/25
Y1 - 2020/7/25
N2 - In this study, a greener and stable surface-active cobalt-carbonyl like specie [HCo(CO)y] was generated via H2 and CO spillover by gold on ion-promoted cobalt oxide. The supports and catalysts syntheses were based on inverse micelle and deposition-precipitation methods, respectively. The temperature-programmed reduction was used for optimization to obtain the best supports. The catalysts with activity (Co3O4 < Cs-Co3O4 < Au/Cs-Co3O4 and Au loadings 10 % < 2 % < 5 %) were evaluated for the hydroformylation-hydrogenation of alkenes to alcohols, with the 5 % Au/Cs-Co3O4 catalyst more active than the others and displayed excellent alcohol chemoselectivity with varying regioselectivity under milder reaction conditions. The reaction was assumed to take place via the formation of [HCo(CO)y] specie, as the active catalytic site of the catalyst. The enhanced catalytic performance was also ascribed to the low-temperature reducibility and surface basicity of the nanomaterials. The stability of the catalyst was evaluated by recycling, with its mesostructure retained after four cycles.
AB - In this study, a greener and stable surface-active cobalt-carbonyl like specie [HCo(CO)y] was generated via H2 and CO spillover by gold on ion-promoted cobalt oxide. The supports and catalysts syntheses were based on inverse micelle and deposition-precipitation methods, respectively. The temperature-programmed reduction was used for optimization to obtain the best supports. The catalysts with activity (Co3O4 < Cs-Co3O4 < Au/Cs-Co3O4 and Au loadings 10 % < 2 % < 5 %) were evaluated for the hydroformylation-hydrogenation of alkenes to alcohols, with the 5 % Au/Cs-Co3O4 catalyst more active than the others and displayed excellent alcohol chemoselectivity with varying regioselectivity under milder reaction conditions. The reaction was assumed to take place via the formation of [HCo(CO)y] specie, as the active catalytic site of the catalyst. The enhanced catalytic performance was also ascribed to the low-temperature reducibility and surface basicity of the nanomaterials. The stability of the catalyst was evaluated by recycling, with its mesostructure retained after four cycles.
KW - 1-octene
KW - Alcohol
KW - Gold catalyst
KW - Hydroformylation-Hydrogenation
KW - Ion-promoters
KW - Mesoporous cobalt
UR - http://www.scopus.com/inward/record.url?scp=85087876689&partnerID=8YFLogxK
U2 - 10.1016/j.apcata.2020.117735
DO - 10.1016/j.apcata.2020.117735
M3 - Article
AN - SCOPUS:85087876689
SN - 0926-860X
VL - 602
JO - Applied Catalysis A: General
JF - Applied Catalysis A: General
M1 - 117735
ER -