A new mechanochemical method was developed to convert polymer wastes, polyethylene (PE), polypropylene (PP), and polyvinyl chloride (PVC), to fuel gases (H2, CH4, and CO) under ball-milling with KMnO4 at room temperature. By using various solid-state characterizations (XPS, SEM, EDS, FTIR, and NMR), and density functional theory calculations, it was found that the activation followed the hydrogen atom transfer (HAT) mechanism. Two metal oxidant molecules were found to abstract two separate hydrogen atoms from the α–CH and β–CH units of substrates, [–βCH2–αCH(R)–]n, where R = H in PE, R =γCH3 in PP, and R = Cl in PVC, resulting in a di-radical, [–βCH•–αC• (R)–]. Subsequently, the two unpaired electrons of the di-radical were recombined into an alkene intermediate, [–βCH =αC(R)–], which underwent further oxidation to produce H2, CH4, and CO gases. Copyright © 2021 by the authors.
|Publication status||Published - Oct 2021|
CitationChow, C.-F., Lam, C.-S., Lau, K.-C., & Gong, C.-B. (2021). Waste-to-energy: Production of fuel gases from plastic wastes. Polymers, 13(21). Retrieved from https://doi.org/10.3390/polym13213672
- Polymer degradation
- C-H bond activation
- Hydrogen atom transfer