TY - JOUR
T1 - Co-generation of hydroxyl and sulfate radicals via homogeneous and heterogeneous bi-catalysis with the EO-PS-EF tri-coupling system for efficient removal of refractory organic pollutants
AU - Yang, Wanlin
AU - Deng, Zejun
AU - Liu, Libin
AU - Zhou, Kechao
AU - E, Peisan (Sharel)
AU - Meng, Lingcong
AU - Ma, Li
AU - Wei, Qiuping
N1 - Funding Information:
We gratefully acknowledge the National Key Research and Development Program of China (No. 2021YFB3701800 ), the National Natural Science Foundation of China (No. 52202056 , No. 52274370 , No. 52071345 , No. 51874370 ), the Province Key Research and Development Program of Guangdong (No. 2020B010185001 ), the Province High-tech Industry Science and Technology Innovation Leading Plan of Hunan (No. 2022GK4037 , No. 2022GK4047 ), the Independent and Open projects of the State Key Laboratory of Powder Metallurgy (No. 621022230 ), and the High Performance Computing Center of Central South University for financial support.
Publisher Copyright:
© 2023
PY - 2023/7/5
Y1 - 2023/7/5
N2 - Advanced oxidation processes are commonly considered one of the most effective techniques to degrade refractory organic pollutants, but the limitation of a single process usually makes it insufficient to achieve the desired treatment. This work introduces, for the first time, a highly-efficient coupled advanced oxidation process, namely Electro-Oxidation—Persulfate—Electro-Fenton (EO-PS-EF). Leveraging the EO-PS-EF tri-coupling system, diverse contaminants can be highly efficiently removed with the help of reactive hydroxyl and sulfate radicals generated via homogeneous and heterogeneous bi-catalysis, as certified by radical quenching and electron spin resonance. Concerning degradation of tetracycline (TC), the EO-PS-EF system witnessed a fast pseudo-first-order reaction kinetic constant of 2.54 × 10−3 s−1, ten times that of a single EO system and three-to-four times that of a binary system (EO-PS or EO-EF). In addition, critical parameters (e.g., electrolyte, pH and temperature) are systematically investigated. Surprisingly, after 100 repetitive trials TC removal can still reach 100% within 30 min and no apparent morphological changes to electrode materials were observed, demonstrating its long-term stability. Finally, its universality was demonstrated with effective degradation of diverse refractory contaminants (i.e., antibiotics, dyes and pesticides).
AB - Advanced oxidation processes are commonly considered one of the most effective techniques to degrade refractory organic pollutants, but the limitation of a single process usually makes it insufficient to achieve the desired treatment. This work introduces, for the first time, a highly-efficient coupled advanced oxidation process, namely Electro-Oxidation—Persulfate—Electro-Fenton (EO-PS-EF). Leveraging the EO-PS-EF tri-coupling system, diverse contaminants can be highly efficiently removed with the help of reactive hydroxyl and sulfate radicals generated via homogeneous and heterogeneous bi-catalysis, as certified by radical quenching and electron spin resonance. Concerning degradation of tetracycline (TC), the EO-PS-EF system witnessed a fast pseudo-first-order reaction kinetic constant of 2.54 × 10−3 s−1, ten times that of a single EO system and three-to-four times that of a binary system (EO-PS or EO-EF). In addition, critical parameters (e.g., electrolyte, pH and temperature) are systematically investigated. Surprisingly, after 100 repetitive trials TC removal can still reach 100% within 30 min and no apparent morphological changes to electrode materials were observed, demonstrating its long-term stability. Finally, its universality was demonstrated with effective degradation of diverse refractory contaminants (i.e., antibiotics, dyes and pesticides).
KW - Application potential
KW - Degradation pathway
KW - Electro-Oxidation—Persulfate—Electro-Fenton
KW - Hydroxyl and sulfate radicals
KW - Mechanism
U2 - 10.1016/j.watres.2023.120312
DO - 10.1016/j.watres.2023.120312
M3 - Article
C2 - 37453402
AN - SCOPUS:85164657624
SN - 0043-1354
VL - 243
JO - Water Research
JF - Water Research
M1 - 120312
ER -