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Ionizing radiation induced degradation of diuron in dilute aqueous solution
BACKGROUND: Cutting edge technologies based on Advanced Oxidation Processes (AOP) are under development for the elimination of highly persistent organic molecules (like pesticides) from water matrices. Among them, ionizing radiation treatment represents a promising technology that requires no additi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415950/ https://www.ncbi.nlm.nih.gov/pubmed/25937832 http://dx.doi.org/10.1186/s13065-015-0097-0 |
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author | Kovács, Krisztina He, Shijun Mile, Viktoria Csay, Tamás Takács, Erzsébet Wojnárovits, László |
author_facet | Kovács, Krisztina He, Shijun Mile, Viktoria Csay, Tamás Takács, Erzsébet Wojnárovits, László |
author_sort | Kovács, Krisztina |
collection | PubMed |
description | BACKGROUND: Cutting edge technologies based on Advanced Oxidation Processes (AOP) are under development for the elimination of highly persistent organic molecules (like pesticides) from water matrices. Among them, ionizing radiation treatment represents a promising technology that requires no additives and can be easily adapted to an industrial scale. In these processes several reactive species are produced, mainly powerful oxidizing radicals inducing the degradation. This paper investigates the reactions taking place in dilute aqueous solutions of a hazardous pollutant (diuron) during irradiation. RESULTS: Irradiation of aqueous diuron solutions resulted in effective degradation of the solute mainly due to the reactions of hydroxyl radicals formed in water radiolysis. Hydroxyl radical reacts with diuron with a second order rate constant of (5.8 ± 0.3) × 10(9) mol(−1) dm(3) s(−1). The main reaction is addition to the ring forming hydroxycyclohexadienyl radical. 30 − 50% of hydroxyl radical reactions induce dechlorination. Reactions with the methyl groups or with the α-amino group have low contribution to the transformation. The presence of dissolved oxygen enhances the rate of degradation; one hydroxyl radical on average induces five-electron oxidations. The high oxidation rate is attributed to the reaction of some of the primarily formed organic radicals with dissolved O(2) and the subsequent reactions of the peroxy radicals. CONCLUSION: The presence of dissolved oxygen is highly important to achieve efficient ionizing radiation induced degradation of diuron in dilute aqueous solution. |
format | Online Article Text |
id | pubmed-4415950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-44159502015-05-02 Ionizing radiation induced degradation of diuron in dilute aqueous solution Kovács, Krisztina He, Shijun Mile, Viktoria Csay, Tamás Takács, Erzsébet Wojnárovits, László Chem Cent J Research Article BACKGROUND: Cutting edge technologies based on Advanced Oxidation Processes (AOP) are under development for the elimination of highly persistent organic molecules (like pesticides) from water matrices. Among them, ionizing radiation treatment represents a promising technology that requires no additives and can be easily adapted to an industrial scale. In these processes several reactive species are produced, mainly powerful oxidizing radicals inducing the degradation. This paper investigates the reactions taking place in dilute aqueous solutions of a hazardous pollutant (diuron) during irradiation. RESULTS: Irradiation of aqueous diuron solutions resulted in effective degradation of the solute mainly due to the reactions of hydroxyl radicals formed in water radiolysis. Hydroxyl radical reacts with diuron with a second order rate constant of (5.8 ± 0.3) × 10(9) mol(−1) dm(3) s(−1). The main reaction is addition to the ring forming hydroxycyclohexadienyl radical. 30 − 50% of hydroxyl radical reactions induce dechlorination. Reactions with the methyl groups or with the α-amino group have low contribution to the transformation. The presence of dissolved oxygen enhances the rate of degradation; one hydroxyl radical on average induces five-electron oxidations. The high oxidation rate is attributed to the reaction of some of the primarily formed organic radicals with dissolved O(2) and the subsequent reactions of the peroxy radicals. CONCLUSION: The presence of dissolved oxygen is highly important to achieve efficient ionizing radiation induced degradation of diuron in dilute aqueous solution. Springer International Publishing 2015-04-18 /pmc/articles/PMC4415950/ /pubmed/25937832 http://dx.doi.org/10.1186/s13065-015-0097-0 Text en © Kovács et al.; licensee Springer. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kovács, Krisztina He, Shijun Mile, Viktoria Csay, Tamás Takács, Erzsébet Wojnárovits, László Ionizing radiation induced degradation of diuron in dilute aqueous solution |
title | Ionizing radiation induced degradation of diuron in dilute aqueous solution |
title_full | Ionizing radiation induced degradation of diuron in dilute aqueous solution |
title_fullStr | Ionizing radiation induced degradation of diuron in dilute aqueous solution |
title_full_unstemmed | Ionizing radiation induced degradation of diuron in dilute aqueous solution |
title_short | Ionizing radiation induced degradation of diuron in dilute aqueous solution |
title_sort | ionizing radiation induced degradation of diuron in dilute aqueous solution |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415950/ https://www.ncbi.nlm.nih.gov/pubmed/25937832 http://dx.doi.org/10.1186/s13065-015-0097-0 |
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