Приказ основних података о документу

dc.contributor.authorPergal, Marija
dc.contributor.authorKodranov, Igor
dc.contributor.authorDojčinović, Biljana
dc.contributor.authorAvdin, Viacheslav
dc.contributor.authorStanković, Dalibor
dc.contributor.authorPetković, Branka
dc.contributor.authorManojlović, Dragan
dc.date.accessioned2023-04-13T07:05:01Z
dc.date.available2023-04-13T07:05:01Z
dc.identifier.citationMinistry of Education, Science and Technological Development of the Republic of Serbia (Grant No. 451-03-68/2020-14/200026)en_US
dc.identifier.citationMinistry of Education, Science and Technological Development of the Republic of Serbia (Grant No. 451-03-68/2020-14/ 200168)en_US
dc.identifier.citationTwinOxide-RS d.o.o.en_US
dc.identifier.urihttps://platon.pr.ac.rs/handle/123456789/1200
dc.description.abstractChlorine dioxide (ClO2) degradation of the organophosphorus pesticides azamethiphos (AZA) and dimethoate (DM) (10 mg/L) in deionized water and in Sava River water was investigated for the first time. Pesticide degradation was studied in terms of ClO2 level (5 and 10 mg/L), degradation duration (0.5, 1, 2, 3, 6, and 24 h), pH (3.00, 7.00, and 9.00), and under light/dark conditions in deionized water. Degradation was monitored using high-performance liquid chromatography. Gas chromatography coupled with triple quadrupole mass detector was used to identify degradation products of pesticides. Total organic carbon was measured to determine the extent of mineralization after pesticide degradation. Real river water was used under recommended conditions to study the influence of organic matter on pesticide degradation. High degradation efficiency (88–100% for AZA and 85–98% for DM) was achieved in deionized water under various conditions, proving the flexibility of ClO2 degradation for the examined organophosphorus pesticides. In Sava River water, however, extended treatment duration achieved lower degradation efficiency, so ClO2 oxidized both the pesticides and dissolved organic matter in parallel. After degradation, AZA produced four identified products (6-chlorooxazolo[4,5-b]pyridin-2(3H)-one; O,O,S-trimethyl phosphorothioate; 6-chloro-3-(hydroxymethyl)oxazolo[4,5- b]pyridin-2(3H)-one; O,O-dimethyl S-hydrogen phosphorothioate) and DM produced three (O,O-dimethyl S-(2-(methylamino)-2-oxoethyl) phosphorothioate; e.g., omethoate; S-(2-(methylamino)-2-oxoethyl) O,O-dihydrogen phosphorothioate; O,O,S-trimethyl phosphorodithioate). Simple pesticide degradation mechanisms were deduced. Daphnia magna toxicity tests showed degradation products were less toxic than parent compounds. These results contribute to our understanding of the multiple influences that organophosphorus pesticides and their degradation products have on environmental ecosystems and to improving pesticide removal processes from water.en_US
dc.language.isoen_USen_US
dc.titleEvaluation of azamethiphos and dimethoate degradation using chlorine dioxide during water treatmenten_US
dc.title.alternativeEnvironmental Science and Pollution Researchen_US
dc.typeclanak-u-casopisuen_US
dc.description.versionpublishedVersionen_US
dc.identifier.doihttps://doi.org/10.1007/s11356-020-09069-5
dc.citation.volume27
dc.citation.spage27147
dc.citation.epage27160
dc.subject.keywordsRiver water sampleen_US
dc.subject.keywordsOrganophosphorus pesticidesen_US
dc.subject.keywordsChlorine dioxide treatmenten_US
dc.subject.keywordsWater qualityen_US
dc.subject.keywordsEcotoxicityen_US
dc.subject.keywordsGas chromatography with triple quad mass detectoren_US
dc.type.mCategoryM21en_US
dc.type.mCategoryclosedAccessen_US
dc.type.mCategoryM21en_US
dc.type.mCategoryclosedAccessen_US


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Приказ основних података о документу