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

Charles O. Oseghale, Batsile M. Mogudi, Christianah A. Akinnawo, Reinout Meijboom

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)

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 languageEnglish
Article number117735
JournalApplied Catalysis A: General
Volume602
DOIs
Publication statusPublished - 25 Jul 2020

Keywords

  • 1-octene
  • Alcohol
  • Gold catalyst
  • Hydroformylation-Hydrogenation
  • Ion-promoters
  • Mesoporous cobalt

ASJC Scopus subject areas

  • Catalysis
  • Process Chemistry and Technology

Fingerprint

Dive into the research topics of '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'. Together they form a unique fingerprint.

Cite this