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Degradation kinetics and transformation pathway of methyl parathion by δ-MnO 2 /oxalic acid reaction system.

Authors :
Wang J
Yue W
Teng Y
Zhai Y
Zhu H
Source :
Chemosphere [Chemosphere] 2023 Apr; Vol. 320, pp. 138054. Date of Electronic Publication: 2023 Feb 03.
Publication Year :
2023

Abstract

Methyl parathion (MP) is a typical organophosphorus pesticide that is widely used worldwide, and hydrolysis, oxidation and reduction are the main abiotic degradation processes. Manganese dioxide (MnO <subscript>2</subscript> ) and organic acid can participate in various geochemical processes of pollutants, a reaction system was constructed to degrade MP using δ-MnO <subscript>2</subscript> and oxalic acid. The δ-MnO <subscript>2</subscript> /oxalic acid reaction system could efficiently degrade MP, and the removal rate of MP (20 μM) reached 67.83% within 30 h under the optimized conditions (pH 5, [δ-MnO <subscript>2</subscript> ] = 2 mM, [oxalic acid] = 100 mM). MP was hydrolyzed by substitution reactions of S <subscript>N</subscript> @P and S <subscript>N</subscript> @C, and reduced by conversion of the nitro groups (-NO <subscript>2</subscript> ) in MP and its hydrolysates to amino groups (-NH <subscript>2</subscript> ). The primary active substance produced in the reaction system was the complexes dominated by Mn(III)-oxalic acid. This study provides a scientific basis for the degradation of organophosphorus pesticides using MnO <subscript>2</subscript> and an organic acid. The results have important theoretical significance and application value for pollution control and remediation of organophosphorus pesticides.<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 :
320
Database :
MEDLINE
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
36739984
Full Text :
https://doi.org/10.1016/j.chemosphere.2023.138054