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Highly selective hydrogenation of phenol to cyclohexanone over a Pd-loaded N-doped carbon catalyst derived from chitosan...

by Qiong Wu, Arthur J Ragauskas
Publication Type
Journal
Journal Name
Journal of Colloid and Interface Science
Publication Date
Page Numbers
82 to 90
Volume
605
Issue
00

A highly stable Pd-loaded N-doped carbon catalyst (ACNpd) for phenol hydrogenation was prepared from chitosan by hydrothermal carbonization. ACNpd does not require a reduction step before catalytic use due to the Pd in the as-prepared catalyst mainly exists in the form of Pd0 (80%). The carbon support involves N-containing groups such as pyridinic nitrogen and pyrrolic nitrogen, which could provide basic sites to adsorb phenol effectively. The as-fabricated ACNpd shows high catalytic performance with turnover frequency (TOF) of 29.34 h−1. Accordingly, a phenol conversion of 100% and a cyclohexanone selectivity of 99.1% are achieved in 5 h at 100 °C and 1 MPa H2. This outstanding performance is attributed to the synergetic effects of the Pd particles, the N-functional groups, and the Lewis acid sites on the support. The carbon support presents intrinsic Lewis acid sites due to its electrophilicity, and Pd doping further increases the strength of such acid sites as it causes electron-deficient structural features. Moreover, the Lewis acid sites inhibit the over-hydrogenation from cyclohexanone to cyclohexanol. This study provides new insights into the application of functional biomass-based carbon materials as catalyst supports.