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Bottle-grade polyethylene furanoate from ring-opening polymerisation of cyclic oligomers

Polyethylene furanoate (PEF) represents a promising renewable resource-based bioplastic as replacement for fossil-based polyethylene terephthalate (PET) with improved material properties. However, the synthesis of PEF through conventional polycondensation remains challenging, since the time-intensiv...

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Autores principales: Rosenboom, Jan-Georg, Hohl, Diana Kay, Fleckenstein, Peter, Storti, Giuseppe, Morbidelli, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057881/
https://www.ncbi.nlm.nih.gov/pubmed/30042388
http://dx.doi.org/10.1038/s41467-018-05147-y
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author Rosenboom, Jan-Georg
Hohl, Diana Kay
Fleckenstein, Peter
Storti, Giuseppe
Morbidelli, Massimo
author_facet Rosenboom, Jan-Georg
Hohl, Diana Kay
Fleckenstein, Peter
Storti, Giuseppe
Morbidelli, Massimo
author_sort Rosenboom, Jan-Georg
collection PubMed
description Polyethylene furanoate (PEF) represents a promising renewable resource-based bioplastic as replacement for fossil-based polyethylene terephthalate (PET) with improved material properties. However, the synthesis of PEF through conventional polycondensation remains challenging, since the time-intensive reaction leads to degradation and undesired discolouration of the product. Here we show the successful rapid synthesis of bottle-grade PEF via ring-opening polymerisation (ROP) from cyclic PEF oligomers within minutes, thereby avoiding degradation and discolouration. The melting point of such mixture of cyclic oligomers lies around 370 °C, well above the degradation temperature of PEF (~329 °C). This challenge can be overcome, exploiting the self-plasticising effect of the forming polymer itself (which melts around 220 °C) by initiation in the presence of a high boiling, yet removable, and inert liquid plasticiser. This concept yields polymer grades required for bottle applications (M(n) > 30 kg mol(−1), conversion > 95%, colour-free products), and can be extended to other diffusion-limited polymer systems.
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spelling pubmed-60578812018-07-26 Bottle-grade polyethylene furanoate from ring-opening polymerisation of cyclic oligomers Rosenboom, Jan-Georg Hohl, Diana Kay Fleckenstein, Peter Storti, Giuseppe Morbidelli, Massimo Nat Commun Article Polyethylene furanoate (PEF) represents a promising renewable resource-based bioplastic as replacement for fossil-based polyethylene terephthalate (PET) with improved material properties. However, the synthesis of PEF through conventional polycondensation remains challenging, since the time-intensive reaction leads to degradation and undesired discolouration of the product. Here we show the successful rapid synthesis of bottle-grade PEF via ring-opening polymerisation (ROP) from cyclic PEF oligomers within minutes, thereby avoiding degradation and discolouration. The melting point of such mixture of cyclic oligomers lies around 370 °C, well above the degradation temperature of PEF (~329 °C). This challenge can be overcome, exploiting the self-plasticising effect of the forming polymer itself (which melts around 220 °C) by initiation in the presence of a high boiling, yet removable, and inert liquid plasticiser. This concept yields polymer grades required for bottle applications (M(n) > 30 kg mol(−1), conversion > 95%, colour-free products), and can be extended to other diffusion-limited polymer systems. Nature Publishing Group UK 2018-07-24 /pmc/articles/PMC6057881/ /pubmed/30042388 http://dx.doi.org/10.1038/s41467-018-05147-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rosenboom, Jan-Georg
Hohl, Diana Kay
Fleckenstein, Peter
Storti, Giuseppe
Morbidelli, Massimo
Bottle-grade polyethylene furanoate from ring-opening polymerisation of cyclic oligomers
title Bottle-grade polyethylene furanoate from ring-opening polymerisation of cyclic oligomers
title_full Bottle-grade polyethylene furanoate from ring-opening polymerisation of cyclic oligomers
title_fullStr Bottle-grade polyethylene furanoate from ring-opening polymerisation of cyclic oligomers
title_full_unstemmed Bottle-grade polyethylene furanoate from ring-opening polymerisation of cyclic oligomers
title_short Bottle-grade polyethylene furanoate from ring-opening polymerisation of cyclic oligomers
title_sort bottle-grade polyethylene furanoate from ring-opening polymerisation of cyclic oligomers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057881/
https://www.ncbi.nlm.nih.gov/pubmed/30042388
http://dx.doi.org/10.1038/s41467-018-05147-y
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