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dc.contributor.authorPatinha, David J. S.
dc.contributor.authorTomé, Liliana C.
dc.contributor.authorIsik, Mehmet ORCID
dc.contributor.authorMecerreyes Molero, David
dc.contributor.authorSilvestre, Armando J. D.
dc.contributor.authorMarrucho, Isabel M.
dc.date.accessioned2018-06-19T09:17:22Z
dc.date.available2018-06-19T09:17:22Z
dc.date.issued2017-09
dc.identifier.citationMaterials 10(9) : (2016) // Article ID 1094es_ES
dc.identifier.issn1996-1944
dc.identifier.urihttp://hdl.handle.net/10810/27608
dc.description.abstractCrosslinked pyrrolidinium-based poly(ionic liquids) (Pyrr-PILs) were synthesized through a fast, simple, and solventless photopolymerization scheme, and tested as solid phase microextraction (SPME) sorbents. A series of Pyrr-PILs bearing three different alkyl side chain lengths with two, eight, and fourteen carbons was prepared, characterized, and homogeneously coated on a steel wire by using a very simple procedure. The resulting coatings showed a high thermal stability, with decomposition temperatures above 350 degrees C, excellent film stability, and lifetime of over 100 injections. The performance of these PIL-based SPME fibers was evaluated using a mixture of eleven organic compounds with different molar volumes and chemical functionalities (alcohols, ketones, and monoterpenes). The Pyrr-PIL fibers were obtained as dense film coatings, with 67 mu m thickness, with an overall sorption increase of 90% and 55% as compared to commercial fibers of Polyacrylate (85 mu m) (PA85) and Polydimethylsiloxane (7 mu m) (PDMS7) coatings, respectively. A urine sample doped with the sample mixture was used to study the matrix effect and establish relative recoveries, which ranged from 60.2% to 104.1%.es_ES
dc.description.sponsorshipDavid J. S. Patinha, and Liliana C. Tome are grateful to FCT (Fundacao para a Ciencia e a Tecnologia) for the PhD research grant SFRH/BD/97042/2013 and the Post-Doctoral research grant (SFRH/BPD/101793/2014), respectively. David J. S. Patinha also thanks the financial support from COST-Exil Project 1206. The NMR data was acquired at CERMAX (Centro de Ressonncia Magnetica Antnio Xavier) which is a member of the National NMR network. This work was partially supported by FCT through Research Unit GREEN-it " Bioresources for Sustainability" (UID/Multi/04551/2013) and the Associate Laboratory CICECO Aveiro Institute of materials (UID/CTM/50011/2013).es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectsolid phase microextractiones_ES
dc.subjectpoly(ionic liquids)es_ES
dc.subjectUV-photopolymerizationes_ES
dc.subjectgas chromatographyes_ES
dc.subjectsteel coatingses_ES
dc.subjectfiberses_ES
dc.subjectpolymeric ionic liquides_ES
dc.subjectsorbent coatingses_ES
dc.subjectextractiones_ES
dc.subjectsilicaes_ES
dc.subjectwateres_ES
dc.subjectchemistryes_ES
dc.subjectsystemses_ES
dc.subjectfiberses_ES
dc.titleExpanding the Applicability of Poly(Ionic Liquids) in Solid Phase Microextraction: Pyrrolidinium Coatingses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttp://www.mdpi.com/1996-1944/10/9/1094es_ES
dc.identifier.doi10.3390/ma10091094
dc.departamentoesFísica de materialeses_ES
dc.departamentoeuMaterialen fisikaes_ES


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2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access
article distributed under the terms and conditions of the Creative Commons Attribution
(CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).