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Decoration of CeO2 nanoparticles on g-C3N4 for degradation of microcystins through photocatalytic activation of peroxymonosulfate

  • Shilin Yang
  • , Xia Wang
  • , Peng Jin
  • , Anzhong Peng
  • , Kezhen Qi*
  • , Jieli He
  • , Alireza Khataee*
  • *Bu çalışma için yazışmadan sorumlu yazar
  • Dali University
  • University of Tabriz

Araştırma sonucu: Dergiye katkıMakalebilirkişi

30 Atıf (Scopus)

Özet

As the most common cyanobacterial toxin, microcystin LR (MC-LR) has dangerous neurotoxicity and hepatotoxicity, posing a serious threat to human and ecosystem health. Therefore, we constructed a type-II CeO2/g-C3N4 heterojunction for highly efficient degradation of MC-LR via peroxymonosulfate (PMS) assisted-visible light-driven photocatalysis process. Multi techniques were conducted to analyze the microstructures, optical and electrochemical properties of CeO2/g-C3N4. The experimental results indicate that the composite material has appropriate energy levels and establishes a well-established interfacial band structure, facilitating the migration and separation of photogenerated electron-hole pairs. The coupled photocatalysis and PMS activation system presented a dramatically enhanced catalytic performance. Within 60 min, 10% CeO2/g-C3N4/PMS could degrade 99% of the MC-LR present in the solution under visible light irradiation, which was about 3.8 times higher than that in a single photocatalytic system. The optimal conditions for this degradation process were a PMS dosage of 3.0 mM and an initial pH of 2.5. EPR analysis revealed that SO4ˉ, O2ˉ, h+, and 1O2 were involved in the degradation process. Moreover, the intermediates of its degradation were analyzed through UPLC-MS. This study provides a valuable resource for the intelligent development of type-II heterojunction and its practical implications in the photodegradation of MC-LR through synergistic activation with PMS.

Orijinal dilİngilizce
Makale numarası174794
DergiJournal of Alloys and Compounds
Hacim995
DOI'lar
Yayın durumuYayınlandı - 15 Ağu 2024

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Publisher Copyright:
© 2024 Elsevier B.V.

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