Gas-phase selective oxidation of cyclohexanol to cyclohexanone over Au/Mg1-xCuxCr2O4 catalysts: On the role of Cu doping
Highlights
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Oxidation catalyst developed: gold nanoparticles dispersed on Cu-doped spinel MgCr2O4.
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Highly active and selective catalysts for gas-phase oxidation of cyclohexanol.
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Au
Cu synergy due to O2 activation on Cu species, Au catalyzes CH bond activation. - •
Au
Cu alloy formed during catalytic operation. - •
>99% cyclohexanol conversion and >90% cyclohexanone selectivity obtained.
Abstract
The industrial production of cyclohexanone from cyclohexanol would benefit from a selective oxidation catalyst. Herein, Cu doping of MgCr2O4 supports for gold nanoparticles active in gas-phase oxidation of cyclohexanol was investigated. Mg1-xCuxCr2O4 exhibited spinel structures (x ≤ 0.25: MgCr2O4; x = 1: CuCr2O4) onto which 3–4 nm gold nanoparticles could be dispersed. Cu doping led to higher activity. During reaction, surface Cu2+ was reduced to Cu0, resulting in AuCu alloy formation. At low temperature, low-Cu-content catalysts (x ≤ 0.1) showed higher activity than high-Cu-content catalysts, likely because the AuCu alloy with highly diluted Cu was more active for the dehydrogenation step of cyclohexanol. However, Au/Mg0.99Cu0.01Cr2O4 and Au/Mg0.9Cu0.1Cr2O4 showed lower cyclohexanol conversion at high temperature than samples with high Cu content, because O2 activation involving Cu becomes rate-limiting. Stable cyclohexanol conversion and cyclohexanone selectivity were 99.1% and 90.2% (space-time yield of 266 gKetone gAu−1 h−1) for Au/Mg0.25Cu0.75Cr2O4 at 300 °C.
