Removal of polyethylene terephthalate plastics waste via Co–CeO2 photocatalyst–activated peroxymonosulfate strategy
[Display omitted] •Co–CeO2 was used to activate the PMS for degrading PET plastics.•The degradation rate reached 91.61 % in 6 h after adding 1 mL H2O2 and 5 mM PMS.•Several factors, such as pH and anions, were considered.•SO4− played a crucial role in the degradation, compared to OH, O2−, and 1O2.•T...
Gespeichert in:
Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2024-01, Vol.479, p.147781, Article 147781 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | [Display omitted]
•Co–CeO2 was used to activate the PMS for degrading PET plastics.•The degradation rate reached 91.61 % in 6 h after adding 1 mL H2O2 and 5 mM PMS.•Several factors, such as pH and anions, were considered.•SO4− played a crucial role in the degradation, compared to OH, O2−, and 1O2.•The possible mechanism of photocatalysis/PMS degradation of PET was proposed.
Polyethylene terephthalate (PET) plastic, widely used for packaging owing to its excellent properties, has become a major contributor to plastic waste, for which satisfactory recycling and upgrading treatment technologies are lacking. In this study, Co-doped CeO2 was used as a photocatalyst to degrade PET plastics in water, and PET degradation was measured according to the weight loss rate. Peroxymonosulfate (PMS) addition to the photocatalytic system enabled the degradation of 53.82 ± 4.48 % of PET plastics, highlighting the excellent PET plastic degradation capability of the photocatalytic PMS system. The study investigated the effects of the catalyst-to-plastic ratio, PMS concentration, initial pH, inorganic anions, humic acid concentration, and hydrogen peroxide (H2O2) addition on the catalytic oxidation system. Contrast experiments revealed that H2O2 addition to the photocatalysis/PMS oxidation system further improved the PET plastic degradation efficiency (91.61 ± 1.50 %). Liquid product analysis, electron paramagnetic resonance, and free radical quenching experiments confirmed that SO4− played the most significant role in PET degradation. Finally, a possible mechanism for the degradation of PET plastics in water using the photocatalysis/PMS oxidation system was proposed. |
---|---|
ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2023.147781 |