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<OAI-PMH schemaLocation=http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd> <responseDate>2018-01-15T18:32:37Z</responseDate> <request identifier=oai:HAL:hal-00878024v1 verb=GetRecord metadataPrefix=oai_dc>http://api.archives-ouvertes.fr/oai/hal/</request> <GetRecord> <record> <header> <identifier>oai:HAL:hal-00878024v1</identifier> <datestamp>2017-12-21</datestamp> <setSpec>type:ART</setSpec> <setSpec>subject:sdv</setSpec> <setSpec>collection:UNIV-AG</setSpec> <setSpec>collection:IFR140</setSpec> <setSpec>collection:GIP-BE</setSpec> <setSpec>collection:UNIV-RENNES1</setSpec> <setSpec>collection:IRSET</setSpec> <setSpec>collection:IRSET-LERES</setSpec> <setSpec>collection:BIOSIT</setSpec> <setSpec>collection:UR1-UFR-SVE</setSpec> <setSpec>collection:STATS-UR1</setSpec> <setSpec>collection:UR1-HAL</setSpec> <setSpec>collection:EHESP</setSpec> <setSpec>collection:USPC</setSpec> <setSpec>collection:UR1-SDV</setSpec> <setSpec>collection:IRSET-EHESP</setSpec> <setSpec>collection:UNIV-ANGERS</setSpec> </header> <metadata><dc> <publisher>HAL CCSD</publisher> <title lang=en>MSPE/UV for field detection of micropollutants in water</title> <creator>Brogat, Marine</creator> <creator>Cadiere, Axelle</creator> <creator>Thomas, Olivier</creator> <creator>Baurès, Estelle</creator> <creator>Roig, Benoit</creator> <contributor>Institut de recherche, santé, environnement et travail [Rennes] (Irset) ; Université d'Angers (UA) - Université des Antilles et de la Guyane (UAG) - Université de Rennes 1 (UR1) - École des Hautes Études en Santé Publique [EHESP] (EHESP) - Institut National de la Santé et de la Recherche Médicale (INSERM) - Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )</contributor> <contributor>École des Hautes Études en Santé Publique [EHESP] (EHESP)</contributor> <contributor>Laboratoire d'étude et de recherche en environnement et santé (LERES) ; École des Hautes Études en Santé Publique [EHESP] (EHESP)</contributor> <contributor>This work was supported by the French Ministry of Industry in the frame of the 2010 Eco-Industries call for project.</contributor> <description>International audience</description> <source>ISSN: 0026-265X</source> <source>EISSN: 1095-9149</source> <source>Microchemical Journal</source> <publisher>Elsevier</publisher> <identifier>hal-00878024</identifier> <identifier>https://hal.archives-ouvertes.fr/hal-00878024</identifier> <source>https://hal.archives-ouvertes.fr/hal-00878024</source> <source>Microchemical Journal, Elsevier, 2013, 108, pp.215-223. 〈10.1016/j.microc.2012.10.025〉</source> <identifier>DOI : 10.1016/j.microc.2012.10.025</identifier> <relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.microc.2012.10.025</relation> <language>en</language> <subject lang=en>Detection</subject> <subject lang=en>Micropollutants</subject> <subject lang=en>Water</subject> <subject lang=en>Diagnosis</subject> <subject lang=en>Field</subject> <subject>[SDV.EE] Life Sciences [q-bio]/Ecology, environment</subject> <type>info:eu-repo/semantics/article</type> <type>Journal articles</type> <description lang=en>This paper proposes a new approach for the on-site detection of micropollutants in water in case of accidental or intentional contamination (characterized by high concentration). The technique is based on the use of an automatic multiple solid phase extraction step (MSPE) followed by direct or indirect UV spectrometry (MSPE/UV) for the detection of organic contaminants in water (such as regulated molecules (pesticides ...) as well as emerging pollutants (pharmaceutical products, endocrine disruptors ...)). The development of the system supposes firstly the choice of the most appropriate sorbent(s) and secondly conditions for the detection of targeted micropollutants, from several solid phase extraction cartridges and eluting solvents. Two different extraction sorbents were chosen. These sorbents and several eluting solvents allow the first separation of the compounds based on the physico-chemical properties of each substance (pKa, log Kow) and on the specific interactions with the sorbent. Finally, a UV analysis (either at the maximum of absorbance using a calibration curve or from the whole spectrum using a multicomponent (deconvolution) exploitation method) of each fraction allows a determination and a quantification of each compound. The method is rapid (less than 2 h), sensitive enough for an accidental/intentional contamination (between 5 and 40 μg*L− 1 according to the substances) and with a good precision (between 4 and 14%).</description> <date>2013-05</date> </dc> </metadata> </record> </GetRecord> </OAI-PMH>