Efficient activation of peroxyacetic acid by cobalt-iron alloy/oxide heterojunctions anchored in defect-rich biochar for pesticide degradation in water: Unravelling the radical-unradical mechanism

[Display omitted] •CoFe@DBC2.0–700 has excellent catalytic activity in activating PAA to degrade pesticides.•The inherent defects in biochar accelerate electron transfer between CoFe alloy/oxide heterojunctions.•The removal of 2,4-D is facilitated through dual pathways involving both radical and non...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2024-11, Vol.500, p.156810, Article 156810
Hauptverfasser: Liang, Xuetao, Li, Xueying, Zhao, Yujie, Li, Jingran, Liu, Bingyang, Yang, Qingbang, Cui, Longyan, Yang, Zhilin, Yang, Qi
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:[Display omitted] •CoFe@DBC2.0–700 has excellent catalytic activity in activating PAA to degrade pesticides.•The inherent defects in biochar accelerate electron transfer between CoFe alloy/oxide heterojunctions.•The removal of 2,4-D is facilitated through dual pathways involving both radical and non-radical mechanisms.•CoFe@DBC2.0–700/PAA system reduces the biotoxicity of pesticide wastewater. The activation processes of peracetic acid (PAA-AOPs) have garnered significant attention in wastewater treatment. In this study, an amorphous carbon-modified bimetallic CoFe alloy/oxide catalyst (CoFe@DBCx-y, where x represents biomass mass and y represents pyrolysis temperature) was developed to activate PAA for the degradation of organochlorine pesticides (OCPs). Due to the size effect, biochar dynamically regulates the particle size of metal species, which is influenced by the pyrolysis temperature. Among these systems, the CoFeDBC2.0–700/PAA oxidation system effectively removed 95.7 % of 2,4-dichlorophenoxyacetic acid (2,4-D), exhibiting a kinetic constant 1.7 times higher than that of the Nano/PAA system. Furthermore, quenching experiments and electron paramagnetic resonance (EPR) analysis revealed that high-valent metal oxides (MIV = O) and singlet oxygen (1O2) are the primary active species responsible for the removal of 2,4-D, whereas organic radicals (RO·) and hydroxyl radicals (·OH) play a secondary role. Electrochemical and Raman spectroscopy tests revealed the formation of a metastable surface complex (≡Co(III)–OO(O)CCH3) between PAA and the catalyst, which acted as an intermediate oxidant to generate reactive oxygen species (ROS) through a chain reaction. Carbon defects in the biochar functioned as an electron source, continuously replenishing the electrons consumed in the reaction and facilitating the valence cycling between Co and Fe. This study provides new insights into the remediation of pesticide-contaminated wastewater using PAA-AOPs with heterogeneous bimetallic carbon-based catalysts.
ISSN:1385-8947
DOI:10.1016/j.cej.2024.156810