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Interfacial complexation between Fe3+ and Bi2MoO6 promote efficient persulfate activation via Fe3+/Fe2+ cycle for organic contaminates degradation upon visible light irradiation.

Authors :
Bai, Chengbo
Zhang, Yuhan
Liu, Qiong
Zhu, Chengxin
Li, Jun
Chen, Rong
Source :
Journal of Colloid & Interface Science. Jun2024, Vol. 664, p238-250. 13p.
Publication Year :
2024

Abstract

[Display omitted] • Interfacial complexation of Fe3+ and Bi 2 MoO 6 is established in the presence of PDS. • The complexation between Fe3+ and Bi 2 MoO 6 accelerates the Fe3+/Fe2+ cycle. • Efficient organic contaminants degradation is achieved by Bi 2 MoO 6 /Fe3+/PDS/Vis system. • The Fe3+/Fe2+ redox cycle is employed to promote the continuous activation of PDS. To address the observed decrease in efficiency during Fe2+-mediated persulfate (PDS) activation caused by slow electron transfer rates and challenges in cycling between Fe3+/Fe2+ states, we devised a strategy to establish interfacial complexation between Fe3+ and Bi 2 MoO 6 in the presence of PDS. The proposed approach facilitates more efficient capture of photogenerated electrons, thereby accelerating the rate-limiting reduction process of the Fe3+/Fe2+ cycle under visible light irradiation and promoting PDS activation. The Bi 2 MoO 6 /Fe3+/PDS/Vis system demonstrates complete degradation of organic pollutants, including Atrazine (ATZ), carbamazepine (CBZ), bisphenol A (BPA), and 2,4-dichlorophenol (DCP) at a concentration of 10 mg/L within a rapid reaction time of 30 min. Radical scavenging experiments and electron paramagnetic resonance spectra (EPR) confirm that the sulfate radical (•SO 4 −) is the dominant species responsible for organic contaminant degradation. The real-time conversion process between Fe3+ and Fe2+ was monitored by observing changes in iron species forms and concentrations within the reaction system. X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy verify the formation of a complexation between Fe3+ and Bi 2 MoO 6 , facilitating anchoring of Fe3+ onto material surface. Based on these findings, we propose a reliable mechanism for the activation reaction. This work presents a promising heterogeneous PDS activation method based on Fe3+/Fe2+ cycle for water treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219797
Volume :
664
Database :
Academic Search Index
Journal :
Journal of Colloid & Interface Science
Publication Type :
Academic Journal
Accession number :
176390964
Full Text :
https://doi.org/10.1016/j.jcis.2024.03.024