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Assessment of photo electro-Fenton and solar photo electro-Fenton processes for the efficient degradation of asulam herbicide.

Authors :
Vigil-Castillo HH
Ruiz-Ruiz EJ
López-Velázquez K
Hinojosa-Reyes L
Gaspar-Ramírez O
Guzmán-Mar JL
Source :
Chemosphere [Chemosphere] 2023 Oct; Vol. 338, pp. 139585. Date of Electronic Publication: 2023 Jul 19.
Publication Year :
2023

Abstract

The degradation of asulam herbicide by photo electro-Fenton (PEF) and solar photo electro-Fenton (SPEF) processes was studied using an undivided electrochemical BDD/carbon-felt cell to generate H <subscript>2</subscript> O <subscript>2</subscript> continuously. A central composite design combined with response surface methodology was applied to determine the optimal operating conditions of current intensity = 0.30 A, [Fe <superscript>2+</superscript> ] = 0.3 mM, and [Na <subscript>2</subscript> SO <subscript>4</subscript> ] = 0.11 M at pH 3 to achieve the complete degradation of asulam by electro-Fenton. Subsequently, the SPEF process was more efficient treatment compared to PEF, achieving a complete degradation of asulam and 98% of mineralization in 180 min. Moreover, 4-aminobenzenesulfonamide, 4-aminophenol, and 4-benzoquinone were detected as aromatic intermediates, whereas acetic acid, oxalic acid, and NO <subscript>3</subscript> <superscript>-</superscript> ions were identified as final degradation by-products. Thus, the SPEF process is an efficient alternative for the complete degradation and mineralization of herbicide asulam in an aqueous solution under natural sunlight.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1879-1298
Volume :
338
Database :
MEDLINE
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
37478989
Full Text :
https://doi.org/10.1016/j.chemosphere.2023.139585