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Polylactide-based networks containing dynamic tetraphenylethane groups for 3D printed repairable and reprocessable constructs

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dc.title Polylactide-based networks containing dynamic tetraphenylethane groups for 3D printed repairable and reprocessable constructs en
dc.contributor.author Borská, Katarína
dc.contributor.author Bednarek, Melania
dc.contributor.author Gorgol, Danila
dc.contributor.author Osička, Josef
dc.contributor.author Mrlík, Miroslav
dc.relation.ispartof Reactive and Functional Polymers
dc.identifier.issn 1381-5148 Scopus Sources, Sherpa/RoMEO, JCR
dc.identifier.issn 1873-166X Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2023
utb.relation.volume 191
dc.type article
dc.language.iso en
dc.publisher Elsevier B.V.
dc.identifier.doi 10.1016/j.reactfunctpolym.2023.105694
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S1381514823001979
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S1381514823001979/pdfft?md5=cbaacafea113279fba2504e990e0b1ca&pid=1-s2.0-S1381514823001979-main.pdf
dc.subject polylactide en
dc.subject reversible-dynamic polymer network en
dc.subject tetraphenylethane en
dc.subject reprocessability en
dc.subject 3D printing en
dc.description.abstract This study aims to synthesize sustainable polylactide (PLA) materials, specifically polyester-urethanes based on PLAs with various molecular weights, to enhance thermal shape stability through crosslinking and enable reprocessing due to the presence of a new type of dynamic/reversible covalent bonds in the polymer structure. PLA-based networks containing dynamic bonds were prepared by coupling (using hexamethylene diisocyanate) PLA star polymers bearing four terminal -OH groups with a low molecular weight diol containing groups that undergo reversible dissociation upon heating. The PLAs prepolymers of two molecular weights (Mn = 3700 and 7800 g/mol) were synthesized via cationic polymerization of D,L-lactide to obtain the networks of different crosslinking densities. The low molecular weight diol, containing a tetraphenylethane moiety (TPE) with an easy dissociating bond, was synthesized from 4-hydroxybenzophenone. Networks without reversible bonds, containing 1,1′-bi-2-naphthol (binol) instead of TPE units, were also prepared as a reference. All networks were analyzed by Fourier transform infrared spectroscopy, differential scanning calorimetry, and thermogravimetric analysis and were subjected to tensile tests. The tensile strength of all networks was in the range of 22–45 MPa. The elongations at break of networks differed based on the type of used low molecular weight diol, with values in the range of 28–67% for TPE-containing networks, in comparison with 10% for reference samples. Rheological studies of these materials were performed at a higher temperature (150 °C) to clearly demonstrate the behavioral differences between networks with and without “reversible” bonds. Only the networks with TPE groups were able to recover their previous strength after strain deformation at 150 °C in four subsequent cycles. Moreover, it was shown that networks with reversible groups were repairable and 3D printable at temperatures as low as 150 °C, while those containing non-reversible bonds did not exhibit such capability. en
utb.faculty University Institute
dc.identifier.uri http://hdl.handle.net/10563/1011687
utb.identifier.obdid 43884923
utb.identifier.scopus 2-s2.0-85169563047
utb.identifier.wok 001067191300001
utb.identifier.coden RFPOF
utb.source j-scopus
dc.date.accessioned 2023-12-05T11:36:29Z
dc.date.available 2023-12-05T11:36:29Z
dc.description.sponsorship DKRVO, (RP/CPS/2022/003); Tomas Bata University in Zlin, TBU, (IGA/CPS/2021/004); Ministerstvo Školství, Mládeže a Tělovýchovy, MŠMT; Narodowe Centrum Nauki, NCN, (2018/31/B/ST8/01969)
dc.description.sponsorship National Science Centre, Poland [2018/31/B/ST8/01969]; Ministry of Education, Youth and Sports of the Czech Republic - DKRVO [RP/CPS/2022/003]; Internal Grant Agency of Tomas Bata University in Zlin [IGA/CPS/2021/004]
utb.ou Centre of Polymeric Systems
utb.contributor.internalauthor Gorgol, Danila
utb.contributor.internalauthor Osička, Josef
utb.contributor.internalauthor Mrlík, Miroslav
utb.fulltext.sponsorship This work was supported by the National Science Centre, Poland, under grant no. 2018/31/B/ST8/01969. Authors M.M. and J.O. gratefully acknowledge the Ministry of Education, Youth and Sports of the Czech Republic - DKRVO (RP/CPS/2022/003). Furthermore, author D. G. would like to gratefully acknowledge to Internal Grant Agency of Tomas Bata University in Zlin (project no. IGA/CPS/2021/004) for financial support.
utb.wos.affiliation [Borska, Katarina; Bednarek, Melania] Polish Acad Sci, Ctr Mol & Macromol Studies, Sienkiewicza 112, PL-90363 Lodz, Poland; [Borska, Katarina] Slovak Acad Sci, Polymer Inst, Dubravska Cesta 9, Bratislava 84541, Slovakia; [Gorgol, Danila; Osicka, Josef; Mrlik, Miroslav] Tomas Bata Univ Zlin, Ctr Polymer Syst, Trida Tomase Bati 5678, Zlin 76001, Czech Republic
utb.scopus.affiliation Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, Lodz, 90-363, Poland; Polymer Institute, Slovak Academy of Sciences, Dubravska Cesta 9, Bratislava, 845 41, Slovakia; Centre of Polymer Systems, Tomas Bata University in Zlin, Trida Tomase Bati 5678, Zlín, 760 01, Czech Republic
utb.fulltext.projects 2018/31/B/ST8/01969
utb.fulltext.projects DKRVO (RP/CPS/2022/003)
utb.fulltext.projects IGA/CPS/2021/004
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