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Updated: Jul 19, 2026

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Upcycling Polyoxymethylene via H2O2-Mediated Selective Oxidation
Mugeng Chen1, Kaizhi Wang1, Zehui Sun1
1Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, State Key Laboratory of Porous Materials for Separation and Conversion, Fudan University, Shanghai, 200438, China.
Abstract:
The increasing challenge of plastic pollution, coupled with the depletion of fossil resources, necessitates innovative solutions for the sustainable management of end-of-life plastics. This issue is particularly pressing for polyoxymethylene (POM), a widely used engineering thermoplastic known for its exceptional mechanical properties and durability, which degrades slowly and releases harmful formaldehyde (HCHO). Herein a straightforward method is presented to convert POM waste into formic acid (FA) using hydrogen peroxide (H2O2) as the oxidant. While H2O2 is recognized as a selective and mild oxidation agent, its potential for upcycling plastics into valuable chemicals has been largely uncharted. The approach utilizes microporous aluminosilicate zeolite H-Beta, known for its Brønsted acidity, to effectively catalyze both the depolymerization of POM into HCHO and its subsequent oxidation to FA. A significant aspect of this method is the incorporation of 1,1,1,3,3,3-hexafluoroisopropanol, which enhances depolymerization through strong hydrogen bonding interactions. This catalytic system efficiently transforms a variety of postconsumer POM waste into FA while also facilitating the Baeyer-Villiger-type oxidation of various carbonyl compounds, achieving high yields in both processes. Overall, these findings advance the conversion of plastic waste into value-added chemicals via H2O2-mediated reactions, enhancing sustainable waste management and supporting circular economy principles.
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