dc.creatorVieira, Camila M.S.
dc.creatorMazurkievicz, Melaine
dc.creatorLopez Calvo, Angela Maria
dc.creatorDebatin, Vítor
dc.creatorMicke, Gustavo Amadeu
dc.creatorRichter Duk, Pablo
dc.creatorRosero-Moreano, Milton
dc.creatorRocha, Eduardo Carasek da
dc.date.accessioned2018-12-20T15:11:45Z
dc.date.available2018-12-20T15:11:45Z
dc.date.created2018-12-20T15:11:45Z
dc.date.issued2018
dc.identifierJournal of Separation Science, Volumen 41, Issue 21, 2018, Pages 4047-4054
dc.identifier16159314
dc.identifier16159306
dc.identifier10.1002/jssc.201800426
dc.identifierhttps://repositorio.uchile.cl/handle/2250/158445
dc.description.abstract© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim In this study, the viability of applying cork and montmorillonite clay modified with ionic liquid as biosorbents in the rotating-disk sorptive extraction technique was investigated. Specifically, this was aimed at the determination of methyl paraben, ethyl paraben, propyl paraben, and isobutyl paraben, with separation/determination by high-performance liquid chromatography coupled with mass spectrometry. The optimization of the method for both biosorbents was performed using multivariate procedures. The extraction efficiencies for the target compounds in aqueous matrices were compared to those obtained using the commercial sorbent Octadecil Silano-C18. The optimum extraction conditions for both natural sorbents were the use of an ammonia solution (pH 10) as desorption solvent and an extraction time of 30 min. The proposed methods show limits of quantification of 0.8 μg/L for cork, 3.0 μg/L for montmorillonite clay and 6.0 μg/L for Octad
dc.languageen
dc.publisherWiley-VCH Verlag
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceJournal of Separation Science
dc.subjectcork
dc.subjectmontmorillonite clay
dc.subjectparabens
dc.subjectrotating-disk sorptive extraction
dc.subjectwater
dc.titleExploiting green sorbents in rotating-disk sorptive extraction for the determination of parabens by high-performance liquid chromatography with tandem electrospray ionization triple quadrupole mass spectrometry
dc.typeArtículo de revista


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