Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/26924
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dc.contributor.authorFaria, Fernando A. C.pt_PT
dc.contributor.authorEvtuguin, Dmitry V.pt_PT
dc.contributor.authorRudnitskaya, Alisapt_PT
dc.contributor.authorGomes, Maria T. S. R.pt_PT
dc.contributor.authorOliveira, João A. B. P.pt_PT
dc.contributor.authorGraça, M. Pedro F.pt_PT
dc.contributor.authorCosta, Luis C.pt_PT
dc.date.accessioned2019-11-07T15:04:15Z-
dc.date.available2019-11-07T15:04:15Z-
dc.date.issued2012-
dc.identifier.issn0959-8103pt_PT
dc.identifier.urihttp://hdl.handle.net/10773/26924-
dc.description.abstractModified eucalyptus kraft lignin doped with multiwall carbon nanotubes (MWCNTs) was used as a macromonomer in stepgrowth polymerization with tolylene 2,4-diisocyanate terminated poly(propylene glycol) with the aim of producing a conductive copolymer for all-solid-state potentiometric chemical sensor applications. The crosslinked elastomeric polyurethane obtained was characterized by Fourier transform infrared attenuated total reflection spectroscopy, scanning electron microscopy, tunnelling electron microscopy and atomic force microscopy. Doping of lignin-based polyurethane with MWCNTs produced a significant enhancement of its electrical conductivity without deterioration of thermal and viscoelastic properties. The polymer composite displayed a low percolation threshold at an MWCNT concentration of 0.18% (w/w), which was explained by the oriented distribution of MWCNTs along lignin clusters. All lignin-based polyurethanes doped with MWCNTs at concentrations above the percolation threshold are suitable for sensor applications.pt_PT
dc.language.isoengpt_PT
dc.publisherWileypt_PT
dc.rightsrestrictedAccesspt_PT
dc.subjectKraft ligninpt_PT
dc.subjectPolyurethanept_PT
dc.subjectCarbon nanotubespt_PT
dc.subjectNanocompositespt_PT
dc.subjectChemical sensorspt_PT
dc.titleLignin-based polyurethane doped with carbon nanotubes for sensor applicationspt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.firstPage788pt_PT
degois.publication.issue5pt_PT
degois.publication.lastPage794pt_PT
degois.publication.titlePolymer Internationalpt_PT
degois.publication.volume61pt_PT
dc.identifier.doi10.1002/pi.4140pt_PT
dc.identifier.essn1097-0126pt_PT
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