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dc.contributor.authorRipollés Vidal, Cristina
dc.contributor.authorMarín Ramos, José Manuel
dc.contributor.authorSancho, Juan V
dc.contributor.authorLopez, Francisco
dc.contributor.authorHernandez, Felix
dc.date.accessioned2012-05-30T06:50:05Z
dc.date.available2012-05-30T06:50:05Z
dc.date.issued2011-11-22
dc.identifier.citationInternational Journal of Environmental Analytical Chemistry (2011) vol. 91, no. 14, pp. 1380-1391ca_CA
dc.identifier.issn0306-7319
dc.identifier.issn1029-0397
dc.identifier.urihttp://hdl.handle.net/10234/39220
dc.description.abstractA detailed analytical study on ethephon residue determination in water, making use of ion-pairing liquid chromatography coupled to electrospray tandem mass spectrometry (LC/MS/MS), has been carried out. Ethephon is a plant growth regulator, highly polar, which is typically present in aqueous solution in anionic form due to its acid character. Both its extraction and pre-concentration from water samples and its chromatographic retention are difficult. Several approaches for sample pretreatment have been tested including direct injection into the chromatographic system, on-line solid phase extraction (SPE) and off-line SPE, with the best results being obtained after off-line SPE, using Oasis MAX cartridges (mixed-mode strong anion-exchange). After testing several ion-pairing reagents, tetrabuthylammonium acetate (TBA) was selected. This was added to the samples before LC/MS/MS analysis to facilitate ethephon chromatographic retention. The acquisition of several specific MS/MS transitions together with the evaluation of their relative intensity ratios allowed the reliable confirmation of the analyte in samples. The optimised approach was tested in low-salinity water spiked at 0.1 µg L−1 level with satisfactory recovery, and a limit of detection of 0.02 µg L−1. To this purpose, the water sample was partially de-ionised in an initial stage, in order to remove major ions that would have interfered in analyses. The application of this methodology to more saline/complex water samples, as surface or wastewater, was problematic and a thorough optimisation of the de-ionisation conditions would be required.ca_CA
dc.format.extent19 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherTaylor & Francisca_CA
dc.relation.isFormatOfVersió pre-print del document publicat a: http://www.tandfonline.com/doi/abs/10.1080/03067319.2010.520131ca_CA
dc.rights© Taylor & Francisca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subjectEthephonca_CA
dc.subjectIon-pairing liquid chromatographyca_CA
dc.subjectTandem mass spectrometryca_CA
dc.subjectTetrabuthylammoniumca_CA
dc.subjectWater analysisca_CA
dc.subject.lcshLiquid chromatographyca_CA
dc.subject.lcshMass spectrometryca_CA
dc.subject.otherCromatografia de líquidsca_CA
dc.subject.otherEspectrometria de massesca_CA
dc.titleAnalytical study on ethephon residue determination in water by ion-pairing liquid chromatography/tandem mass spectrometryca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1080/03067319.2010.520131
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca_CA
dc.type.versioninfo:eu-repo/semantics/submittedVersion


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