Abstract
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.
Original language | English |
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Article number | 117735 |
Journal | Applied Catalysis A: General |
Volume | 602 |
DOIs | |
Publication status | Published - 25 Jul 2020 |
Keywords
- 1-octene
- Alcohol
- Gold catalyst
- Hydroformylation-Hydrogenation
- Ion-promoters
- Mesoporous cobalt
ASJC Scopus subject areas
- Catalysis
- Process Chemistry and Technology