Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Efficient removal of ciprofloxacin via photo-Fenton system under circumneutral condition: Performance and mechanism insight. / Du, Yongxia; Xiao, Yan; Xu, Yin и др.
в: Journal of Environmental Chemical Engineering, Том 13, № 5, 117936, 10.2025.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Efficient removal of ciprofloxacin via photo-Fenton system under circumneutral condition: Performance and mechanism insight
AU - Du, Yongxia
AU - Xiao, Yan
AU - Xu, Yin
AU - Zhang, Wenzhuo
AU - Feng, Jiahao
AU - Zhao, Wenwen
AU - Tang, Huiling
AU - Hai, Xiaomeng
AU - Xu, Jing
AU - Pozdnyakov, Ivan P.
AU - Zhang, Hui
N1 - This work is supported by the National Natural Science Foundation of China (Grant No. 22061132001) and the Russian Science Foundation (Grant RSF-NSFC No. 21–43–00004). We thank the Core Facility of Wuhan University for XPS analyses.
PY - 2025/10
Y1 - 2025/10
N2 - Developing highly efficient processes for ciprofloxacin (CIP) degradation remains a significant challenge owing to its widespread use. Herein, a visible light photo-Fenton system assisted by a magnetic Fe3O4-sepiolite catalyst (Fe3O4-SP-20) fabricated via a facile precipitation method was proposed to effectively eliminate CIP in water. The use of 0.6 g/L Fe3O4-SP-20 catalyst, 40 mM H2O2 and a 500 W Xe lamp led to 89.5 % removal of 0.03 mM CIP in 90 min at circumneutral pH 6.4. The effects of various operating parameters as well as natural water matrices on CIP abatement were explored. To fully investigate the reaction mechanism of the Vis/Fe3O4-SP-20/H2O2 process, comprehensive experiments and characterizations were performed with or without visible light irradiation. Hydroxyl radicals (•OH) could be formed by the activation of H2O2 with Fe3O4-SP-20 in the dark condition. Upon visible light irradiation, photo-generated electrons (e-) from Fe3O4-SP-20 excitation are captured by H2O2, which generates additional •OH radicals and promotes e-/h+ separation, facilitating the effective degradation of CIP by h+. In parallel, the photoinduced electrons participate in the Fe(III)/Fe(II) redox cycle, further enhancing the Fenton-like reaction to promote the generation of •OH. Overall, this study provides a novel perspective on the remediation of refractory organic wastewater using the Vis/Fe3O4-SP-20/H2O2 system.
AB - Developing highly efficient processes for ciprofloxacin (CIP) degradation remains a significant challenge owing to its widespread use. Herein, a visible light photo-Fenton system assisted by a magnetic Fe3O4-sepiolite catalyst (Fe3O4-SP-20) fabricated via a facile precipitation method was proposed to effectively eliminate CIP in water. The use of 0.6 g/L Fe3O4-SP-20 catalyst, 40 mM H2O2 and a 500 W Xe lamp led to 89.5 % removal of 0.03 mM CIP in 90 min at circumneutral pH 6.4. The effects of various operating parameters as well as natural water matrices on CIP abatement were explored. To fully investigate the reaction mechanism of the Vis/Fe3O4-SP-20/H2O2 process, comprehensive experiments and characterizations were performed with or without visible light irradiation. Hydroxyl radicals (•OH) could be formed by the activation of H2O2 with Fe3O4-SP-20 in the dark condition. Upon visible light irradiation, photo-generated electrons (e-) from Fe3O4-SP-20 excitation are captured by H2O2, which generates additional •OH radicals and promotes e-/h+ separation, facilitating the effective degradation of CIP by h+. In parallel, the photoinduced electrons participate in the Fe(III)/Fe(II) redox cycle, further enhancing the Fenton-like reaction to promote the generation of •OH. Overall, this study provides a novel perspective on the remediation of refractory organic wastewater using the Vis/Fe3O4-SP-20/H2O2 system.
KW - Ciprofloxacin
KW - Heterogeneous catalysis
KW - Magnetic clay
KW - Photo-Fenton
KW - Visible light
UR - https://www.scopus.com/pages/publications/105012197471
UR - https://www.mendeley.com/catalogue/d62d8ba2-cdc8-351b-a936-2a67d428ab29/
U2 - 10.1016/j.jece.2025.117936
DO - 10.1016/j.jece.2025.117936
M3 - Article
VL - 13
JO - Journal of Environmental Chemical Engineering
JF - Journal of Environmental Chemical Engineering
SN - 2213-3437
IS - 5
M1 - 117936
ER -
ID: 68687244