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dc.contributor.authorRodríguez-Mozaz, Sara-
dc.contributor.authorLópez de Alda, Miren-
dc.contributor.authorBarceló, Damià-
dc.date.accessioned2009-09-07T08:15:28Z-
dc.date.available2009-09-07T08:15:28Z-
dc.date.issued2004-07-15-
dc.identifier.citationJournal of Chromatography A 1045(1-2): 85-92 (2004)en_US
dc.identifier.issn0021-9673-
dc.identifier.urihttp://hdl.handle.net/10261/16665-
dc.description8 pages, 6 tables.-- PMID: 15378882 [PubMed].-- Printed version published Aug 6, 2004.-- Presented at the 3rd Meeting of the Spanish Association of Chromatography and Related Techniques and the European Workshop: 3rd Waste Water Cluster, Aguadulce (Almeria), Spain, Nov 19–21, 2003.en_US
dc.description.abstractA multi-residue analytical method has been developed for the determination of various classes of selected endocrine disruptors. This method allows the simultaneous extraction and quantification of different estrogens (estradiol, estrone, estriol, estradiol-17-glucuronide, estradiol diacetate, estrone-3-sulfate, ethynyl estradiol and diethylstilbestrol), pesticides (atrazine, simazine, desethylatrazine, isoproturon and diuron), and bisphenol A in natural waters. In the method developed, 500 ml of water are preconcentrated on LiChrolut RP-18 cartridges. Further analysis is carried out by liquid chromatography–mass spectrometry (LC–MS) using atmospheric pressure chemical ionisation (APCI) in the positive ion mode for determination of pesticides and electrospray in the negative ionisation mode for determination of estrogens and bisphenol A. Recoveries for most compounds were between 90 and 119%, except for bisphenol A (81%) and diethylstilbestrol (70%), with relative standard deviations below 20%. Limits of detection ranged between 2 and 15 ng/l. The method was used to study the occurrence of the selected pollutants in surface and groundwater used for abstraction of drinking water in a waterworks and to evaluate the removal efficiency of the different water treatments applied. Water samples from the river, the aquifer, and after each treatment stage (sand filtration, ozonation, activated carbon filtration and post-chlorination) were taken monthly from February to August of 2002. The presence in river water of atrazine, simazine, diuron and bisphenol A were relatively frequent at concentrations usually below 0.1 μg/l. Lower levels, below 0.02 μg/l, were usual for isoproturon. Estrone-3-sulfate and estrone were detected occasionally in the river. Most of the compounds were completely removed during the water treatment, especially after activated carbon filtration.en_US
dc.description.sponsorshipThis work has been supported by the commission of the European communities (Project ARTDEMO EVK1-CT2002-00114), by the Ministerio de Ciencia y Tecnología (Projects BQU2002-10903-E and BQU-2002-10315-E) and by the I3P Program (co-financed by CSIC and European Social Funds).en_US
dc.format.extent22195 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsclosedAccessen_US
dc.subjectWater analysisen_US
dc.subjectEnvironmental analysisen_US
dc.subjectEstrogensen_US
dc.subjectPesticidesen_US
dc.subjectBisphenol Aen_US
dc.subjectEndocrine disruptorsen_US
dc.titleMonitoring of estrogens, pesticides and bisphenol A in natural waters and drinking water treatment plants by solid-phase extraction–liquid chromatography–mass spectrometryen_US
dc.typeartículoen_US
dc.identifier.doi10.1016/j.chroma.2004.06.040-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.chroma.2004.06.040en_US
dc.identifier.e-issn1873-3778-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
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