Magnetic Co-Al Layered Double Hydroxides as Peroxymonosulfate Activator for the Removal of Pesticide Multiresidues

The increasing prevalence of multiclass pesticide residues in aquatic environments poses a significant threat to ecosystems and human health. To address this challenge, magnetic Fe3O4@Co5Al-LDH nanoparticles were synthesized as high-performance, easily recoverable catalysts for the peroxymonosulfate (PMS)-mediated degradation of epoxiconazole, atrazine, and metalaxyl. Under optimized conditions (pH 7.0, 35 mg catalyst, and 4.0 mM PMS), the system achieved 100% degradation of the three coexisting pesticides within 15 min. Quenching experiments and electron paramagnetic resonance (EPR) spectroscopy confirmed that SO4− and •OH radicals were the primary reactive species driving the process. Liquid chromatography–mass spectrometry (LC-MS) analysis identified four intermediates for epoxiconazole, three for atrazine, and four for metalaxyl, facilitating the proposal of distinct degradation pathways. The degradation mechanism revealed that electron transfer between Fe/Co and PMS promoted the generation of reactive oxygen species, leading to dechlorination, hydroxylation, and dealkylation of the pesticides transiently adsorbed on the surface of Fe3O4@Co5Al-LDH. In summary, this study demonstrates that Fe3O4@Co5Al-LDH is an easily recoverable, reusable, and cost-effective catalyst for the simultaneous remediation of complex pesticide mixtures in water.

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Publication Details

Journal
Separations
Published
2026-07-02
DOI
https://doi.org/10.3390/separations13070193
Primary Topic
Advanced oxidation water treatment
Type
article
Field-Weighted Citation Impact
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article

Magnetic Co-Al Layered Double Hydroxides as Peroxymonosulfate Activator for the Removal of Pesticide Multiresidues

Cheng-Xiang HE, Jun Long, Tian Qin, Bing-Yan Du et al.
Separations
Advanced oxidation water treatment
article

Magnetic Co-Al Layered Double Hydroxides as Peroxymonosulfate Activator for the Removal of Pesticide Multiresidues

Cheng-Xiang HE, Jun Long, Tian Qin, Bing-Yan Du, Er-Cheng Zhao, Zi-Ying Zeng, Zhong-Hua Yang
article en

Abstract

The increasing prevalence of multiclass pesticide residues in aquatic environments poses a significant threat to ecosystems and human health. To address this challenge, magnetic Fe3O4@Co5Al-LDH nanoparticles were synthesized as high-performance, easily recoverable catalysts for the peroxymonosulfate (PMS)-mediated degradation of epoxiconazole, atrazine, and metalaxyl. Under optimized conditions (pH 7.0, 35 mg catalyst, and 4.0 mM PMS), the system achieved 100% degradation of the three coexisting pesticides within 15 min. Quenching experiments and electron paramagnetic resonance (EPR) spectroscopy confirmed that SO4− and •OH radicals were the primary reactive species driving the process. Liquid chromatography–mass spectrometry (LC-MS) analysis identified four intermediates for epoxiconazole, three for atrazine, and four for metalaxyl, facilitating the proposal of distinct degradation pathways. The degradation mechanism revealed that electron transfer between Fe/Co and PMS promoted the generation of reactive oxygen species, leading to dechlorination, hydroxylation, and dealkylation of the pesticides transiently adsorbed on the surface of Fe3O4@Co5Al-LDH. In summary, this study demonstrates that Fe3O4@Co5Al-LDH is an easily recoverable, reusable, and cost-effective catalyst for the simultaneous remediation of complex pesticide mixtures in water.

SeparationsVol. 13(7)
Huazhong Agricultural University (CN), Chinese Academy of Geological Sciences (CN), Beijing Academy of Agricultural and Forestry Sciences (CN)
National Natural Science Foundation of China, China Geological Survey
Life in Land
Openalex Percentile: Top 15%
Advanced oxidation water treatment
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