Open AccessUltrasonic coupling with electrical current to effective activation of Persulfate for 2, 4 Dichlorophenoxyacetic acid herbicide degradation: modeling, synergistic effect, and a by-product study
Author(s) -
Jamal Mehralipour,
Majid Kermani
Publication year - 2021
Publication title -
journal of environmental health science and engineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.447
H-Index - 45
ISSN - 2052-336X
DOI - 10.1007/s40201-021-00633-w
Subject(s) - persulfate , acetic acid , oxidizing agent , chemistry , degradation (telecommunications) , nuclear chemistry , 2,4 dichlorophenoxyacetic acid , catalysis , organic chemistry , botany , biology , telecommunications , computer science
In this research work, we investigated the ability of the oxidative degradation of 2, 4-Dichlorophenoxy acetic acid herbicide via ultrasonic-assisted in electro-activation of the persulfate system in the presence of nano-zero valent iron. The effect of experimental parameters such as pH value [4-8], electrical current (0.5-1 A), persulfate concentration (0.25-0.5 mg.l -1 ), nano zero-valent iron dose (0.05-0.1 mg.l -1 ), and initial organic pollutant concentration (50-100 mg.l -1 ) on the ultrasonic-electropersulfate process performance was assessed via central composite design. The combination of ultrasonic waves with the electrochemical process to activation of persulfate showed better efficiency into 2, 4-Dichlorophenoxy acetic acid herbicide degradation compared to their implementation in individual and binary systems. Following optimal conditions (pH = 5.62, 0.80 A applied electrical current, 0.39 mg/L persulfate concentration, 0.07 mg/L nano-zero valent iron, and 50 mg/L 2,4-Dichlorophenoxy acetic acid concentration in 40 min reaction), nearly 91% removal was done. Moreover, the complete removal of 2, 4-Dichlorophenoxy acetic acid, 92% COD, and 88% TOC removal was achieved by this process near 140 min reaction. The scavenging experiment confirmed the role of free oxidizing species in the degradation of 2, 4-Dichlorophenoxy acetic acid during the process. Approximately 50% improved 2, 4-Dichlorophenoxy acetic acid removal in the process against the inclusive efficiency of single mechanisms. The obtained results were fitted to the pseudo-first-order kinetic model with a high correlation coefficient (R 2 = 0.96). Five important intermediate products of 2, 4-D oxidation were 2, 4-dichlorophenol (2, 4-DCP), 2, 6-dichlorophenol (2, 6-DCP), 4, 6 dichlororesorcinol (4, 6-DCR), 2-chlorohydroquinone (2-CHQ), and 2-chloro-1, 4-benzoquinone (2-CBQ). In the end, can be employed as a satisfactory advanced oxidation process in high mineralization of 2, 4-D and refractory organic pollutants.