Vicinal hydroxyl group-inspired selective oxidation of glycerol to glyceric acid on hydroxyapatite supported Pd catalyst

Selective oxidation of glycerol provides a feasible route towards the sustainable synthesis of high value-added chemicals. Herein, the hydroxyapatite (HAP) supported palladium (Pd) species were fabricated by impregnation and subsequent calcination. The as-obtained heterogeneous Pd catalyst afforded not only excellent selectivity to glyceric acid (GLA) up to 90% with 59% conversion of glycerol but also good recyclability by using molecular oxygen as an oxidant under mild conditions. The characterization of catalysts indicated that both the surface basicity and Pd sites on the catalyst played a crucial role in promoting glycerol oxidation. Notably, it demonstrated that the presence of the vicinal hydroxyl group of glycerol molecule can assist the oxidation reaction via forming a coordination between the vicinal hydroxyl group and Ca2+ sites on HAP-derived catalysts. In this catalytic process, the secondary hydroxyl of glycerol kept untouched and the primary hydroxyl of glycerol was converted into carboxyl group, while the Pd species acted as active centers for cooperatively promoting the subsequent oxidation to generate GLA. Additionally, this catalytic system can be extended widely for the oxidative conversion of other vicinal diols into the corresponding alpha-hydroxycarboxylic acids selectively. Isotope labeling experiment using (H2O)-O-18 confirmed that H2O not only acted as solvent but also was involved in the catalytic cycles. On the basis of the results, a possible reaction mechanism has been proposed. The HAP-supported Pd catalytic system has been shown to serve as an effective approach for the upgrading of bio-derived vicinal diols to high value-added chemicals. (C) 2020 Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.

Automated summary

Selective oxidation of glycerol to glyceric acid can be efficiently achieved using a hydroxyapatite-supported palladium catalyst with molecular oxygen as the oxidant. Surface basicity and Pd sites on the catalyst play a crucial role in promoting glycerol oxidation, and the coordination interaction between the vicinal hydroxyl group of glycerol and Ca2+ sites on the catalyst enhances the oxidation reaction. This catalytic system can also be extended to other vicinal diols for selective oxidation.