Upcycling Polyoxymethylene via H<sub>2</sub>O<sub>2</sub>‐Mediated Selective Oxidation

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 (H<sub>2</sub>O<sub>2</sub>) as the oxidant. While H<sub>2</sub>O<sub>2</sub> 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 H<sub>2</sub>O<sub>2</sub>-mediated reactions, enhancing sustainable waste management and supporting circular economy principles.

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Publication Details

Journal
ChemSusChem
Published
2025-03-31
DOI
https://doi.org/10.1002/cssc.202500179
Citations
4
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
2.82
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article

Upcycling Polyoxymethylene via H2O2‐Mediated Selective Oxidation

Jiachen Fei, Wendi Guo, Heyong He, Mugeng Chen et al.
4 citations
ChemSusChem
Carbon dioxide utilization in catalysis
2.82
article

Upcycling Polyoxymethylene via H2O2‐Mediated Selective Oxidation

Jiachen Fei, Wendi Guo, Heyong He, Mugeng Chen, Chen Chen, Yongmei Liu, Ting Yang, Kaizhi Wang, Zehui Sun, Yong Cao
article en
4 citations

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 (H<sub>2</sub>O<sub>2</sub>) as the oxidant. While H<sub>2</sub>O<sub>2</sub> 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 H<sub>2</sub>O<sub>2</sub>-mediated reactions, enhancing sustainable waste management and supporting circular economy principles.

ChemSusChemVol. 18(12)
Fudan University (CN), Collaborative Innovation Center of Chemistry for Energy Materials (CN)
Responsible consumption and production
Openalex Percentile: Top 12%
Carbon dioxide utilization in catalysis
2.82
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