4.8 Article

Selective Production of Glycolic Acid from Cellulose Promoted by Acidic/Redox Polyoxometalates via Oxidative Hydrolysis

Journal

ACS CATALYSIS
Volume 13, Issue 7, Pages 4575-4586

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.2c05568

Keywords

heteropolyacids; double active sites; cellulose; glycolic acid; cascade conversion; oxygen radical

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This study achieved the direct conversion of cellulose to glycolic acid (GA) with a high yield of up to 75% using acidic/redox polyoxometalates (POMs) as catalysts in a one-pot reaction. Among the three POMs studied, H3PMo showed the most promising catalytic activity. The reaction pathway involves the activation of O2 and the crucial role of the reduced form [PMo10 VIMo2VO39]5- in GA production.
The direct conversion of cellulose to glycolic acid (GA) with a high yield of up to 75% is realized using acidic/redox polyoxometalates (POMs) as catalysts in a one-pot reaction. Analysis of the reaction pathway and mechanism for the three POMs H3PMo12O40 (H3PMo), H3PW12O40 (H3PW), and H5PMo10V2O40 (H5PMoV2) by density functional theory calculations and experiments shows that H3PMo is especially promising. Activation of O2 to center dot O2- and 1O2 via one-electron transfer assists the depolymerization process of cellulose by acidic/redox H3PMo. The reduced form [PMo10 VIMo2VO39]5- plays a crucial role in GA production due to its high activity and ability to stabilize the intermediates of the retro-aldol reaction. H3PMo was furthermore complexed by the ionic liquid 1-(3-sulfonic group) propyl-3-methyl imidazolium (MIMPS), which enables easy recovery from the reaction solution due to temperature-responsive properties of the complexes. [MIMPS]H2PMo provides an outstanding GA selectivity of 61% under aerobic conditions and is comparable to the homogeneous H3PMo. Activity and selectivity to GA could be improved to 100 and 75%, respectively, by performing the reaction in the microwave at 190 degrees C for 2 min. The work deepens the insight on cellulosic biomass transformation over POMs by acidic/oxidative synergetic catalysis and contributes to the effort of designing highly active, selective, and multifunctional catalysts.

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