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Polymer labelling with a conjugated polymer-based luminescence probe for recycling in the circular economy

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dc.title Polymer labelling with a conjugated polymer-based luminescence probe for recycling in the circular economy en
dc.contributor.author Kuřitka, Ivo
dc.contributor.author Sedlařík, Vladimír
dc.contributor.author Harea, Diana
dc.contributor.author Harea, Evghenii
dc.contributor.author Urbánek, Pavel
dc.contributor.author Šloufová, Ivana
dc.contributor.author Coufal, Radek
dc.contributor.author Zedník, Jiří
dc.relation.ispartof Polymers
dc.identifier.issn 2073-4360 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2020
utb.relation.volume 12
utb.relation.issue 6
dc.type article
dc.language.iso en
dc.publisher MDPI AG
dc.identifier.doi 10.3390/polym12061226
dc.relation.uri https://www.mdpi.com/2073-4360/12/6/1226
dc.subject polyacetylene en
dc.subject thermoplastics en
dc.subject fluorescence en
dc.subject label en
dc.subject recycling en
dc.subject labelling en
dc.description.abstract In this paper, we present the use of a disubstituted polyacetylene with high thermal stability and quantum yield as a fluorescence label for the identification, tracing, recycling, and eventually anti-counterfeiting applications of thermoplastics. A new method was developed for the dispersion of poly[1-phenyl-2-[p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) into polymer blends. For such purposes, four representative commodity plastics were selected, i.e., polypropylene, low-density polyethylene, poly(methyl methacrylate), and polylactide. Polymer recycling was mimicked by two reprocessing cycles of the material, which imparted intensive luminescence to the labelled polymer blends when excited by proper illumination. The concentration of the labelling polymer in the matrices was approximately a few tens ppm by weight. Luminescence was visible to the naked eye and survived the simulated recycling successfully. In addition, luminescence emission maxima were correlated with polymer polarity and glass transition temperature, showing a marked blueshift in luminescence emission maxima with the increase in processing temperature and time. This blueshift results from the dispersion of the labelling polymer into the labelled polymer matrix. During processing, the polyacetylene chains disentangled, thereby suppressing their intermolecular interactions. Moreover, shear forces imposed during viscous polymer melt mixing enforced conformational changes, which shortened the average conjugation length of PTMSDPA chain segments. Combined, these two mechanisms shift the luminescence of the probe from a solid-to a more solution-like state. Thus, PTMSDPA can be used as a luminescent probe for dispersion quality, polymer blend homogeneity, and processing history, in addition to the identification, tracing, and recycling of thermoplastics. © 2020 by the authors. en
utb.faculty University Institute
dc.identifier.uri http://hdl.handle.net/10563/1009771
utb.identifier.obdid 43881928
utb.identifier.scopus 2-s2.0-85086639069
utb.identifier.wok 000552479400001
utb.identifier.pubmed 32481616
utb.source j-scopus
dc.date.accessioned 2020-07-10T13:51:20Z
dc.date.available 2020-07-10T13:51:20Z
dc.description.sponsorship Czech Science FoundationGrant Agency of the Czech Republic [17-05318S]; Ministry of Education, Youth and Sports of the Czech Republic-Program NPU I [LO1504]
dc.rights Attribution 4.0 International
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.rights.access openAccess
utb.ou Centre of Polymer Systems
utb.contributor.internalauthor Kuřitka, Ivo
utb.contributor.internalauthor Sedlařík, Vladimír
utb.contributor.internalauthor Harea, Diana
utb.contributor.internalauthor Harea, Evghenii
utb.contributor.internalauthor Urbánek, Pavel
utb.fulltext.affiliation Ivo Kuřitka 1*, Vladimír Sedlařík 1, Diana Harea 1, Evghenii Harea 1, Pavel Urbánek 1, Ivana Šloufová 2, Radek Coufal 2, Jiří Zedník 2 1 Centre of Polymer Systems, University Institute, Tomas Bata University in Zlin, Trida Tomase Bati 5678, 760 01 Zlin, Czech Republic; sedlarik@utb.cz (V.S.); dyanaharea@gmail.com (D.H.); harea@utb.cz (E.H.); urbanek@utb.cz (P.U.) 2 Department of Physical and Macromolecular Chemistry, Faculty of Science, Charles University in Prague, Hlavova 2030/8, 128 40 Prague, Czech Republic; ivana.sloufova@natur.cuni.cz (I.Š.); radek.coufal@natur.cuni.cz (R.C.); jiri.zednik@natur.cuni.cz (J.Z.) * Correspondence: kuritka@utb.cz
utb.fulltext.dates Received: 9 April 2020 Accepted: 25 May 2020 Published: 28 May 2020
utb.fulltext.sponsorship This research was funded by a grant from the Czech Science Foundation (project No. 17-05318S). This work was also funded by the Ministry of Education, Youth and Sports of the Czech Republic-Program NPU I (LO1504). The authors would like to thank Carlos V. Melo for editing the manuscript.
utb.wos.affiliation [Kuritka, Ivo; Sedlarik, Vladimir; Harea, Diana; Harea, Evghenii; Urbanek, Pavel] Tomas Bata Univ Zlin, Univ Inst, Ctr Polymer Syst, Trida Tomase Bati 5678, Zlin 76001, Czech Republic; [Sloufova, Ivana; Coufal, Radek; Zednik, Jiri] Charles Univ Prague, Fac Sci, Dept Phys & Macromol Chem, Hlavova 2030-8, Prague 12840, Czech Republic
utb.scopus.affiliation Centre of Polymer Systems, University Institute, Tomas Bata University in Zlin, trida Tomase Bati 5678, Zlin, 76001, Czech Republic; Department of Physical and Macromolecular Chemistry, Faculty of Science, Charles University in Prague, Hlavova 2030/8, Prague, 12840, Czech Republic
utb.fulltext.projects LO1504
utb.fulltext.faculty University Institute
utb.fulltext.faculty University Institute
utb.fulltext.faculty University Institute
utb.fulltext.faculty University Institute
utb.fulltext.faculty University Institute
utb.fulltext.ou Centre of Polymer Systems
utb.fulltext.ou Centre of Polymer Systems
utb.fulltext.ou Centre of Polymer Systems
utb.fulltext.ou Centre of Polymer Systems
utb.fulltext.ou Centre of Polymer Systems
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