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Exceptionally accelerated Fe(III)/Fe(II) redox couple by niobium carbide MXene: A green and long-lasting enhanced Fenton oxidation.

Authors :
Zhang, Zixuan
Zhou, Chenying
Sun, Yiming
Zhou, Peng
Liu, Yang
Zhang, Heng
Du, Ye
He, Chuanshu
Xiong, Zhaokun
Lai, Bo
Source :
Applied Catalysis B: Environmental. Mar2024, Vol. 342, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

Fenton oxidation technology is a widely-used advanced oxidation technology. However, the generation of hydroxyl radicals is restrained by the sluggish recovery of Fe(II), thus affecting its long-lasting performance for water decontamination. Here, a novel niobium carbide (Nb 2 C) MXene material was applied as a green co-catalyst. Nb 2 C MXene can significantly promote Fenton reactions to produce hydroxyl radicals for degrading dimethyl phthalate (DMP) with high efficiency and high stability for long-term operation, which outperforms than various reported co-catalysts. Meanwhile, the Nb 2 C/Fe(III)/H 2 O 2 system is capable of non-selectively degrading a wide spectrum of refractory pollutants. Mechanism investigation reveals that Nb 2 C MXene as an electron donor can straight reduce Fe(III), meanwhile mediate electron shuttle from Fe(II) to H 2 O 2 to strongly expedite the generation of hydroxyl radicals. In addition, four main degradation routes of DMP were proposed. Therefore, this study offers an updated and valid strategy for the refractory organic pollutants elimination by coupling Nb 2 C MXene and Fenton oxidation. [Display omitted] • Nb 2 C MXene outperformed than a variety of co-catalysts of enhanced Fenton system. • The Nb 2 C/Fe(III)/H 2 O 2 can non-selectively degrade a wide spectrum of organic contaminants. • Nb 2 C MXene can provide electrons for direct Fe(III) reduction by cleaving Nb-C bonds. • Nb 2 C MXene can mediate electron transfer between Fe(II) and H 2 O 2 to promote Fenton reaction. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09263373
Volume :
342
Database :
Academic Search Index
Journal :
Applied Catalysis B: Environmental
Publication Type :
Academic Journal
Accession number :
173692917
Full Text :
https://doi.org/10.1016/j.apcatb.2023.123385