Enhanced degradation of 2,4-dichlorphenoxyacetic acid herbicide by CaO2 activated by Fe(II) and ultrasound irradiation: Practical insight and mineralization

CaO 2 was activated by Fe(II) and ultrasound (US) irradiation to degrade 2,4-dichlorphenoxyacetic acid (2,4-D) for the first time. Among transition metals (Fe, Cu, Mn and Co), Fe(II) had the best performance for the activation of CaO 2 . The impact of pH, CaO 2 and Fe(II) concentration was studied,...

Full description

Saved in:
Bibliographic Details
Published inThe Korean journal of chemical engineering Vol. 40; no. 12; pp. 2866 - 2875
Main Authors Eslami, Akbar, Mahdipour, Fayyaz, Maleksari, Hajar Sharifi, Varank, Gamze, Ghasemi, Seyed Mehdi, Nejatian, Parisa, Bagheri, Amin, Madihi-Bidgoli, Soheila
Format Journal Article
LanguageEnglish
Published New York Springer US 01.12.2023
Springer Nature B.V
한국화학공학회
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:CaO 2 was activated by Fe(II) and ultrasound (US) irradiation to degrade 2,4-dichlorphenoxyacetic acid (2,4-D) for the first time. Among transition metals (Fe, Cu, Mn and Co), Fe(II) had the best performance for the activation of CaO 2 . The impact of pH, CaO 2 and Fe(II) concentration was studied, and under optimal situation ∼91% of 2,4-D was degraded during 60 min reaction time. The quenching experiments showed that the hydroxyl radical was the main factor for the destruction of 2,4-D while superoxide anions had a minor role. The bicarbonate ions and acid humic exhibited a strong inhibitory effect on the performance of CaO 2 /US/Fe(II) process. Carbon and chlorine mineralization of 2,4-D degradation was investigated; around 41% of C and 35% of Cl were mineralized during 60 min reaction time. The function of CaO 2 /US/Fe(II) process was studied on real drainage and other organic pollutants, and the results showed that the CaO 2 /US/Fe(II) process can be practical for water treatment. Finally, intermediates of 2,4-D degradation were identified, a pathway was proposed, and the toxicity of intermediates was assessed by ECOSAR software.
ISSN:0256-1115
1975-7220
DOI:10.1007/s11814-023-1405-3