Waste-to-Energy: Production of Fuel Gases from Plastic Wastes
A new mechanochemical method was developed to convert polymer wastes, polyethylene (PE), polypropylene (PP), and polyvinyl chloride (PVC), to fuel gases (H<sub>2</sub>, CH<sub>4</sub>, and CO) under ball-milling with KMnO<sub>4</sub> at room temperature. By using...
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| Autores principales: | , , , |
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| Formato: | article |
| Lenguaje: | EN |
| Publicado: |
MDPI AG
2021
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| Materias: | |
| Acceso en línea: | https://doaj.org/article/b663fc507a7c40cbb6bef184ee2ecfa1 |
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| Sumario: | A new mechanochemical method was developed to convert polymer wastes, polyethylene (PE), polypropylene (PP), and polyvinyl chloride (PVC), to fuel gases (H<sub>2</sub>, CH<sub>4</sub>, and CO) under ball-milling with KMnO<sub>4</sub> 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, [–<sub>β</sub>CH<sub>2</sub>–<sub>α</sub>CH(R)–]<i><sub>n</sub></i>, where R = H in PE, R = <sub>γ</sub>CH<sub>3</sub> in PP, and R = Cl in PVC, resulting in a di-radical, [–<sub>β</sub>CH<sup>•</sup>–<sub>α</sub>C<sup>•</sup>(R)–]. Subsequently, the two unpaired electrons of the di-radical were recombined into an alkene intermediate, [–<sub>β</sub>CH = <sub>α</sub>C(R)–], which underwent further oxidation to produce H<sub>2</sub>, CH<sub>4</sub>, and CO gases. |
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