Carbon-based metal-free catalysts for selective oxidation of glycerol to glycolic acid

Exploring efficient and cheap catalyst for the selective oxidation of glycerol to valuable carboxylic acids is a critical and complicated challenge. Herein, we innovatively realized the efficient oxidation of glycerol to glycolic acid over metal-free catalyst under mild conditions via carbon material defect engineering. Multiple characterizations revealed that the stepwise functionalization of active carbon caused by simple high temperature control is adopted to fine-tune the composition and electronic structure of oxygen -containing functional groups. Specifically, the abundant ester and carboxyl functional groups exhibit stronger electronegativity than the hydroxyl group, and this enhanced electronic coupling effect strengthens the adsorption of glycerol, thus improving the catalytic activity. Kinetic analysis and density functional theory calculations demonstrated that the oxygen-containing functional groups (mainly ester and carboxyl) could promote the C-H bond activation of RCH2O* intermediate and once C-C bond cleav-age of glyceric acid, ensuring the high selectivity of glycolic acid (53.2% over AC-400 catalyst). We anticipate that this work could sheds some light on the application and design of more new type of carbon-based metal-free catalysts in the aqueous phase oxidation of various polyols. (c) 2022 Elsevier Ltd. All rights reserved.

Automated summary

This study innovatively realized the efficient oxidation of glycerol to glycolic acid over a metal-free catalyst under mild conditions through carbon material defect engineering. The stepwise functionalization of active carbon was found to fine-tune the composition and electronic structure of oxygen-containing functional groups, leading to improved catalytic activity. The oxygen-containing functional groups, particularly ester and carboxyl, were found to promote the C-H bond activation and C-C bond cleavage, ensuring high selectivity for glycolic acid.