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Fully lignocellulose-based PET analogues for the circular economy
Polyethylene terephthalate is one of the most abundantly used polymers, but also a significant pollutant in oceans. Due to growing environmental concerns, polyethylene terephthalate alternatives are highly sought after. Here we present readily recyclable polyethylene terephthalate analogues, made en...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9192716/ https://www.ncbi.nlm.nih.gov/pubmed/35697677 http://dx.doi.org/10.1038/s41467-022-30735-4 |
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author | Wu, Xianyuan Galkin, Maxim V. Stern, Tobias Sun, Zhuohua Barta, Katalin |
author_facet | Wu, Xianyuan Galkin, Maxim V. Stern, Tobias Sun, Zhuohua Barta, Katalin |
author_sort | Wu, Xianyuan |
collection | PubMed |
description | Polyethylene terephthalate is one of the most abundantly used polymers, but also a significant pollutant in oceans. Due to growing environmental concerns, polyethylene terephthalate alternatives are highly sought after. Here we present readily recyclable polyethylene terephthalate analogues, made entirely from woody biomass. Central to the concept is a two-step noble metal free catalytic sequence (Cu20-PMO catalyzed reductive catalytic fractionation and Raney Ni mediated catalytic funneling) that allows for obtaining a single aliphatic diol 4-(3-hydroxypropyl) cyclohexan-1-ol in high isolated yield (11.7 wt% on lignin basis), as well as other product streams that are converted to fuels, achieving a total carbon yield of 29.5%. The diol 4-(3-hydroxypropyl) cyclohexan-1-ol is co-polymerized with methyl esters of terephthalic acid and furan dicarboxylic acid, both of which can be derived from the cellulose residues, to obtain polyesters with competitive Mw and thermal properties (T(g) of 70–90 °C). The polymers show excellent chemical recyclability in methanol and are thus promising candidates for the circular economy. |
format | Online Article Text |
id | pubmed-9192716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91927162022-06-15 Fully lignocellulose-based PET analogues for the circular economy Wu, Xianyuan Galkin, Maxim V. Stern, Tobias Sun, Zhuohua Barta, Katalin Nat Commun Article Polyethylene terephthalate is one of the most abundantly used polymers, but also a significant pollutant in oceans. Due to growing environmental concerns, polyethylene terephthalate alternatives are highly sought after. Here we present readily recyclable polyethylene terephthalate analogues, made entirely from woody biomass. Central to the concept is a two-step noble metal free catalytic sequence (Cu20-PMO catalyzed reductive catalytic fractionation and Raney Ni mediated catalytic funneling) that allows for obtaining a single aliphatic diol 4-(3-hydroxypropyl) cyclohexan-1-ol in high isolated yield (11.7 wt% on lignin basis), as well as other product streams that are converted to fuels, achieving a total carbon yield of 29.5%. The diol 4-(3-hydroxypropyl) cyclohexan-1-ol is co-polymerized with methyl esters of terephthalic acid and furan dicarboxylic acid, both of which can be derived from the cellulose residues, to obtain polyesters with competitive Mw and thermal properties (T(g) of 70–90 °C). The polymers show excellent chemical recyclability in methanol and are thus promising candidates for the circular economy. Nature Publishing Group UK 2022-06-13 /pmc/articles/PMC9192716/ /pubmed/35697677 http://dx.doi.org/10.1038/s41467-022-30735-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wu, Xianyuan Galkin, Maxim V. Stern, Tobias Sun, Zhuohua Barta, Katalin Fully lignocellulose-based PET analogues for the circular economy |
title | Fully lignocellulose-based PET analogues for the circular economy |
title_full | Fully lignocellulose-based PET analogues for the circular economy |
title_fullStr | Fully lignocellulose-based PET analogues for the circular economy |
title_full_unstemmed | Fully lignocellulose-based PET analogues for the circular economy |
title_short | Fully lignocellulose-based PET analogues for the circular economy |
title_sort | fully lignocellulose-based pet analogues for the circular economy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9192716/ https://www.ncbi.nlm.nih.gov/pubmed/35697677 http://dx.doi.org/10.1038/s41467-022-30735-4 |
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