Tuning the Interactions in Multiresponsive Complex Coacervate-Based Underwater Adhesives

dc.bibliographicCitation.firstPage100eng
dc.bibliographicCitation.issue1eng
dc.bibliographicCitation.journalTitleInternational journal of molecular scienceseng
dc.bibliographicCitation.volume21eng
dc.contributor.authorDompé, Marco
dc.contributor.authorCedano-Serrano, Francisco J.
dc.contributor.authorVahdati, Mehdi
dc.contributor.authorSidoli, Ugo
dc.contributor.authorHeckert, Olaf
dc.contributor.authorSynytska, Alla
dc.contributor.authorHourdet, Dominique
dc.contributor.authorCreton, Costantino
dc.contributor.authorvan der Gucht, Jasper
dc.contributor.authorKodger, Thomas
dc.contributor.authorKamperman, Marleen
dc.date.accessioned2021-11-04T10:15:44Z
dc.date.available2021-11-04T10:15:44Z
dc.date.issued2020
dc.description.abstractIn this work, we report the systematic investigation of a multiresponsive complex coacervate-based underwater adhesive, obtained by combining polyelectrolyte domains and thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) units. This material exhibits a transition from liquid to solid but, differently from most reactive glues, is completely held together by non-covalent interactions, i.e., electrostatic and hydrophobic. Because the solidification results in a kinetically trapped morphology, the final mechanical properties strongly depend on the preparation conditions and on the surrounding environment. A systematic study is performed to assess the effect of ionic strength and of PNIPAM content on the thermal, rheological and adhesive properties. This study enables the optimization of polymer composition and environmental conditions for this underwater adhesive system. The best performance with a work of adhesion of 6.5 J/m2 was found for the complex coacervates prepared at high ionic strength (0.75 M NaCl) and at an optimal PNIPAM content around 30% mol/mol. The high ionic strength enables injectability, while the hydrated PNIPAM domains provide additional dissipation, without softening the material so much that it becomes too weak to resist detaching stress. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/7174
dc.identifier.urihttps://doi.org/10.34657/6221
dc.language.isoengeng
dc.publisherBasel : Molecular Diversity Preservation Internationaleng
dc.relation.doihttps://doi.org/10.3390/ijms21010100
dc.relation.essn1422-0067
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc570eng
dc.subject.ddc540eng
dc.subject.otherBioinspired materialseng
dc.subject.otherComplex coacervateeng
dc.subject.otherEnvironmentally-triggered setting processeng
dc.subject.otherLCSTeng
dc.subject.otherNon-covalent interactionseng
dc.subject.otherPoly(N-isopropylacrylamide)eng
dc.subject.otherPolyelectrolyteseng
dc.subject.otherUnderwater adhesioneng
dc.titleTuning the Interactions in Multiresponsive Complex Coacervate-Based Underwater Adhesiveseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPFeng
wgl.subjectBiowissensschaften/Biologieeng
wgl.typeZeitschriftenartikeleng
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