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dc.rights.licenseopenen_US
hal.structure.identifierEnvironnements et Paléoenvironnements OCéaniques [EPOC]
dc.contributor.authorYASSINE, Montaha
hal.structure.identifierNational Council of Scientific Research (NCSR), Lebanese Atomic Energy Commission (LAEC), Laboratory of Analysis of Organic Pollutants (LAOP), B. P. 11- 8281, Riad El Solh, 1107 2260, Beirut, Lebanon.
dc.contributor.authorRIFAI, Ahmad
hal.structure.identifierFaculty of Public Health-Section I, Beyrouth, Lebanon
dc.contributor.authorHOTEIT, Maha
hal.structure.identifierEnvironnements et Paléoenvironnements OCéaniques [EPOC]
dc.contributor.authorMAZELLIER, Patrick
hal.structure.identifierNational Council of Scientific Research (NCSR), Lebanese Atomic Energy Commission (LAEC), Laboratory of Analysis of Organic Pollutants (LAOP), B. P. 11- 8281, Riad El Solh, 1107 2260, Beirut, Lebanon; Faculty of Public Health-Section I, Beyrouth, Lebanon.
dc.contributor.authorAL ISKANDARANI, Mohammad
dc.date.accessioned2024-10-07T12:41:20Z
dc.date.available2024-10-07T12:41:20Z
dc.date.issued2017-12
dc.identifier.issn0045-6535en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/202293
dc.description.abstractEnThis study was conducted to gain a better understanding of the fate of fluoroquinolone antibacterial ofloxacin (OFX) which is the free available chlorine (FAC) in order to determine its effect during water chlorination process. The Direct reactions of FAC with OFX were quite rapid. A half-life of 7.7 s was measured under pseudo-first order conditions in the presence of an excess of total chlorine ([FAC]0 = 13 μM and [OFX]0 = 0.55 μM at pH 7.2 and 20 °C in buffered reagent water. Free chlorine reactions rates were of first-order type in both substrate and oxidant with specific second-order rate constants of 6.8 × 103 M-1 s-1. No induced back reactions or other interference by using thiosulfate to stop the chlorination reaction was shown. The seven products of the reaction were determined by using the LC/MS/MS analysis. Structures were investigated due to the explication of transitions obtained at different CID energies by LC-ESI-MS/MS. Pathways of the formations of these by-products were presented in this study and pathways of the fragmentations of pseudo molecular ions of the structures proposed were presented in supplementary files.
dc.language.isoENen_US
dc.subject.enGEOF
dc.subject.enChlorination
dc.subject.enDegradation
dc.subject.enFormation and fragmentation pathways
dc.subject.enKinetic study
dc.subject.enLCMSMS
dc.subject.enOfloxacine
dc.title.enStudy of the degradation process of ofloxacin with free chlorine by using ESI-LCMSMS: Kinetic study, by-products formation pathways and fragmentation mechanisms
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.chemosphere.2017.08.171en_US
dc.subject.halChimieen_US
bordeaux.journalChemosphereen_US
bordeaux.page46-54en_US
bordeaux.volume189en_US
bordeaux.hal.laboratoriesEPOC : Environnements et Paléoenvironnements Océaniques et Continentaux - UMR 5805en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.teamLPTCen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcehal
hal.identifierhal-03272605
hal.version1
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccPas de Licence CCen_US
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