Determination of four bisphenols in water and urine samples by magnetic dispersive solid‐phase extraction using a modified zeolite/iron oxide composite prior to liquid chromatography diode array detection

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dc.contributorEspectroscopía Atómica-Masas y Química Analítica en Condiciones Extremases_ES
dc.contributor.authorBaile, Paola-
dc.contributor.authorMedina, Juan-
dc.contributor.authorVidal, Lorena-
dc.contributor.authorCanals, Antonio-
dc.contributor.otherUniversidad de Alicante. Departamento de Química Analítica, Nutrición y Bromatologíaes_ES
dc.contributor.otherUniversidad de Alicante. Instituto Universitario de Materialeses_ES
dc.date.accessioned2020-05-27T14:20:32Z-
dc.date.available2020-05-27T14:20:32Z-
dc.date.issued2020-05-
dc.identifier.citationJournal of Separation Science. 2020, 43(9-10): 1808-1816. doi:10.1002/jssc.201901022es_ES
dc.identifier.issn1615-9306 (Print)-
dc.identifier.issn1615-9314 (Online)-
dc.identifier.urihttp://hdl.handle.net/10045/107027-
dc.description.abstractA novel approach is presented to determine four bisphenols in water and urine samples, employing magnetic dispersive solid‐phase extraction combined with liquid chromatography and diode array detection. A modified zeolite‐based magnetic composite was used as an efficient sorbent, combining the advantages of magnetic materials with the remarkable properties of zeolites. A multivariate optimization design was employed to optimize some experimental factors affecting magnetic dispersive solid‐phase extraction. The method was evaluated under optimized conditions (i.e., amount of sorbent, 50 mg; sample pH, unadjusted; NaCl concentration, 1.25%; extraction and elution time, 2 min; eluent solvent, ethanol; eluent solvent volume, 400 µL), obtaining good linearity with correlation coefficients ranging between 0.995 and 0.999 (N = 5) (from 2 to 250 µg/L for bisphenol A, bisphenol AP, and bisphenol P and from 5 to 250 µg/L for bisphenol AF). Method repeatability was assessed obtaining coefficients of variation between 3 and 11% (n = 6). Finally, the method was applied to spiked real samples, obtaining for water samples relative recoveries between 83 and 105%, and for urine samples between 81 and 108% for bisphenol A, bisphenol AP, and bisphenol AF, and between 47 and 59% for bisphenol P.es_ES
dc.description.sponsorshipThe authors would like to thank the Spanish Ministry of Economy and Competitiveness and European Union (FEDER funds) (project no. CTQ2016-79991-R) and Generalitat Valenciana (Spain) (project no. PROMETEO/2018/087) for the financial support. P. Baile also thanks Ministry of Education, Culture and Sports for her FPU grant (FPU14/04589).es_ES
dc.languageenges_ES
dc.publisherWiley-VCH Verlag GmbH & Co. KGaAes_ES
dc.rights© 2019 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheimes_ES
dc.subjectBisphenolses_ES
dc.subjectMagnetic dispersive solid-phase extractiones_ES
dc.subjectUrine sampleses_ES
dc.subjectWater sampleses_ES
dc.subjectZeoliteses_ES
dc.subject.otherNutrición y Bromatologíaes_ES
dc.subject.otherQuímica Analíticaes_ES
dc.titleDetermination of four bisphenols in water and urine samples by magnetic dispersive solid‐phase extraction using a modified zeolite/iron oxide composite prior to liquid chromatography diode array detectiones_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.peerreviewedsies_ES
dc.identifier.doi10.1002/jssc.201901022-
dc.relation.publisherversionhttps://doi.org/10.1002/jssc.201901022es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2016-79991-R-
dc.relation.projectIDinfo:eu-repo/grantAgreement/MECD//FPU14%2F04589-
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