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Synthesis and Verification of Biobased Terephthalic Acid from Furfural

Exploiting biomass as an alternative to petrochemicals for the production of commodity plastics is vitally important if we are to become a more sustainable society. Here, we report a synthetic route for the production of terephthalic acid (TPA), the monomer of the widely used thermoplastic polymer p...

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Autores principales: Tachibana, Yuya, Kimura, Saori, Kasuya, Ken-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4316194/
https://www.ncbi.nlm.nih.gov/pubmed/25648201
http://dx.doi.org/10.1038/srep08249
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author Tachibana, Yuya
Kimura, Saori
Kasuya, Ken-ichi
author_facet Tachibana, Yuya
Kimura, Saori
Kasuya, Ken-ichi
author_sort Tachibana, Yuya
collection PubMed
description Exploiting biomass as an alternative to petrochemicals for the production of commodity plastics is vitally important if we are to become a more sustainable society. Here, we report a synthetic route for the production of terephthalic acid (TPA), the monomer of the widely used thermoplastic polymer poly(ethylene terephthalate) (PET), from the biomass-derived starting material furfural. Biobased furfural was oxidised and dehydrated to give maleic anhydride, which was further reacted with biobased furan to give its Diels-Alder (DA) adduct. The dehydration of the DA adduct gave phthalic anhydride, which was converted via phthalic acid and dipotassium phthalate to TPA. The biobased carbon content of the TPA was measured by accelerator mass spectroscopy and the TPA was found to be made of 100% biobased carbon.
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spelling pubmed-43161942015-02-11 Synthesis and Verification of Biobased Terephthalic Acid from Furfural Tachibana, Yuya Kimura, Saori Kasuya, Ken-ichi Sci Rep Article Exploiting biomass as an alternative to petrochemicals for the production of commodity plastics is vitally important if we are to become a more sustainable society. Here, we report a synthetic route for the production of terephthalic acid (TPA), the monomer of the widely used thermoplastic polymer poly(ethylene terephthalate) (PET), from the biomass-derived starting material furfural. Biobased furfural was oxidised and dehydrated to give maleic anhydride, which was further reacted with biobased furan to give its Diels-Alder (DA) adduct. The dehydration of the DA adduct gave phthalic anhydride, which was converted via phthalic acid and dipotassium phthalate to TPA. The biobased carbon content of the TPA was measured by accelerator mass spectroscopy and the TPA was found to be made of 100% biobased carbon. Nature Publishing Group 2015-02-04 /pmc/articles/PMC4316194/ /pubmed/25648201 http://dx.doi.org/10.1038/srep08249 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Tachibana, Yuya
Kimura, Saori
Kasuya, Ken-ichi
Synthesis and Verification of Biobased Terephthalic Acid from Furfural
title Synthesis and Verification of Biobased Terephthalic Acid from Furfural
title_full Synthesis and Verification of Biobased Terephthalic Acid from Furfural
title_fullStr Synthesis and Verification of Biobased Terephthalic Acid from Furfural
title_full_unstemmed Synthesis and Verification of Biobased Terephthalic Acid from Furfural
title_short Synthesis and Verification of Biobased Terephthalic Acid from Furfural
title_sort synthesis and verification of biobased terephthalic acid from furfural
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4316194/
https://www.ncbi.nlm.nih.gov/pubmed/25648201
http://dx.doi.org/10.1038/srep08249
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