4.5 Article

Insights into Microstructure and Surface Properties of Pd/C for Liquid Phase Phenol Hydrogenation to Cyclohexanone

Journal

CATALYSIS LETTERS
Volume 153, Issue 1, Pages 208-218

Publisher

SPRINGER
DOI: 10.1007/s10562-022-03973-w

Keywords

Microstructure; Surface properties; Phenol hydrogenation; Cyclohexanone; Pd/C; Activated carbon

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Activated carbon supports obtained from different sources were used for the synthesis of Pd/C catalysts in phenol hydrogenation. The results showed that the Pd/C catalyst using activated carbon derived from wood exhibited superior catalytic activity compared to those using activated carbon derived from coconut shell and coal. The enhanced activity of Pd/C-W was attributed to its larger surface area, higher surface N and O contents, more surface defects, and abundant acidic and alkaline sites.
Phenol hydrogenation over Pd/C is a promising technology to produce cyclohexanone, but how to select the carbon supports is not clear. Herein, three types of activated carbon, i.e., produced from coal (C-C), coconut shell (C-CS) and wood (C-W), were selected for the synthesis of Pd/C. The Pd/C catalysts show significant differences in the phenol hydrogenation, and the catalytic activity is in the order of Pd/C-W > Pd/C-CS > Pd/C-C. For example, the phenol conversion of Pd/C-W is 81.6% in dichloromethane, about 4 times higher than that of Pd/C-C. Moreover, Pd/C-W can achieve a phenol conversion of 97.2% with a cyclohexanone selectivity of 97.4% in n-hexane, and has good reusability during at least five reaction cycles. Larger surface area, higher surface N and O contents, more surface defects, abundant acidic and alkaline sites are the key reasons for the superior catalytic activity of Pd/C-W as compared to Pd/C-CS and Pd/C-C. Graphical Abstract The type of activated carbon has a remarkable effect on the microstructure and surface properties of Pd/C, and the corresponding catalytic properties for the liquid phase phenol hydrogenation to cyclohexanone. Larger surface area, higher surface N and O contents, more surface defects, abundant acidic and alkaline sites are the key reasons for the superior catalytic activity of Pd/C-W as compared to Pd/C-CS and Pd/C-C. [GRAPHICS]

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