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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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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. |
format | Online Article Text |
id | pubmed-6057881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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