Reaction mechanism and kinetics for Pt/CNTs catalyzed base-free oxidation of glycerol.

Highlights • Water-assisted O 2 activation to form active OH∗ intermediates is in equilibrium. • The OH∗ species-assisted C H bond cleavage of glycerol is the possible RDS. • The oxidation of the primary and secondary hydroxyl groups have similar mechanism. Abstract Fundamental understanding of heterogeneously catalyzed aerobic, base-free oxidation of glycerol is highly desirable for sustainable and highly efficient chemical synthesis. In this work, Pt/CNTs catalyzed base-free oxidation of glycerol is investigated by combining experiments, DFT calculations and kinetics analysis. The solvent effects and kinetic isotope effects measurements as well as DFT calculations reveal that water-assisted O 2 activation to form active OH∗ intermediates is not in rate-determining step (RDS) but in equilibrium. Then, Langmuir-Hinshelwood kinetic models are developed and fitted with the experimental data. The OH∗-assisted C H bond cleavage of glycerol is discriminated as the RDS for the two parallel oxidation pathways of glycerol via primary or secondary hydroxyl groups, where the former case exhibits lower activation energy. The insights revealed here could guide the design and optimization of this catalytic process to generate the targeted products. [ABSTRACT FROM AUTHOR]