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dc.contributor.authorKupai, Jozsef
dc.contributor.authorRazali, Mayamin
dc.contributor.authorBüyüktiryaki, Sibel
dc.contributor.authorKeçili, Rüstem
dc.contributor.authorSzekely, Gyorgy
dc.date.accessioned2019-10-23T17:56:20Z
dc.date.available2019-10-23T17:56:20Z
dc.date.issued2017
dc.identifier.issn1759-9954
dc.identifier.issn1759-9962
dc.identifier.urihttps://dx.doi.org/10.1039/c6py01853j
dc.identifier.urihttps://hdl.handle.net/11421/22923
dc.descriptionWOS: 000394960900004en_US
dc.descriptionPubMed ID: 28496524en_US
dc.description.abstractMolecularly imprinted materials are man-made mimics of biological receptors. Their polymer network has recognition sites complementary to a substrate in terms of size, shape and chemical functionality. They have diverse applications in various chemical, biomedical and engineering fields such as solid phase extraction, catalysis, drug delivery, pharmaceutical purification, (bio) sensors, water treatment, membrane separations and proteomics. The stability and reusability of molecularly imprinted polymers (IPs) have crucial roles in developing applications that are reliable, economic and sustainable. In the present article the effect of crosslinkers, functional monomers and conditions for template extraction on the long-term stability and reusability of IPs was systematically investigated. Adsorption capacity, selectivity, morphology and thermal decomposition of eleven different L-phenylalanine methyl ester imprinted polymers were studied to reveal performance loss over 100 adsorption-regeneration cycles. Furthermore, crosslinker and functional monomer specific reversible and irreversible decomposition of imprinted polymers as a result of adsorbent regeneration were investigated through adsorption studies, electron microscopy, N-2 adsorption and thermogravimetric analysis. A decomposition mechanism was proposed and revealed using NMR spectroscopy. Solutions to avoid or overcome the limitations of the most common crosslinkers, functional monomers and extraction techniques were proposed and experimentally validated.en_US
dc.description.sponsorshipRoyal Academy of Engineering's Newton Research Collaboration Programme [NRCP1516/1/41]; Hungarian Scientific Research Fund/National Research Development Office, Hungary (OTKA/NKFIH) [PD108462]; 'BioProNET BIV Nov15 Szekely' from BioProNET, a BBSRC Network in Biotechnology and Bioenergy; EPSRCen_US
dc.description.sponsorshipUseful discussions and analytical insights provided by Peter Pogany from Gedeon Richter Plc are greatly acknowledged. The authors thank Patrick Hill and Christos Didaskalou for their technical assistance with SEM analysis. The financial support for RK, SB and GS through the Royal Academy of Engineering's Newton Research Collaboration Programme under grant code NRCP1516/1/41 is greatly acknowledged. The financial support for JK through the Hungarian Scientific Research Fund/National Research Development Office, Hungary (OTKA/NKFIH no. PD108462) is acknowledged. MR and GS would like to acknowledge the funding under grant reference 'BioProNET BIV Nov15 Szekely' from BioProNET, a BBSRC Network in Biotechnology and Bioenergy, co-sponsored by the EPSRC.en_US
dc.language.isoengen_US
dc.publisherRoyal Soc Chemistryen_US
dc.relation.isversionof10.1039/c6py01853jen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleLong-term stability and reusability of molecularly imprinted polymersen_US
dc.typearticleen_US
dc.relation.journalPolymer Chemistryen_US
dc.contributor.departmentAnadolu Üniversitesi, Yunus Emre Sağlık Hizmetleri Meslek Yüksekokuluen_US
dc.identifier.volume8en_US
dc.identifier.issue4en_US
dc.identifier.startpage666en_US
dc.identifier.endpage673en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US]
dc.contributor.institutionauthorBüyüktiryaki, Sibel
dc.contributor.institutionauthorKeçili, Rüstem


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