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Structural Analysis of Lignin-Based Furan Resin

The global “carbon emission peak” and “carbon neutrality” strategic goals promote us to replace current petroleum-based resin products with biomass-based resins. The use of technical lignins and hemicellulose-derived furfuryl alcohol in the production of biomass-based resins are among the most promi...

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Autores principales: Zhu, Xuhai, Bruijnaers, Bardo, Lourençon, Tainise V., Balakshin, Mikhail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746157/
https://www.ncbi.nlm.nih.gov/pubmed/35009496
http://dx.doi.org/10.3390/ma15010350
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author Zhu, Xuhai
Bruijnaers, Bardo
Lourençon, Tainise V.
Balakshin, Mikhail
author_facet Zhu, Xuhai
Bruijnaers, Bardo
Lourençon, Tainise V.
Balakshin, Mikhail
author_sort Zhu, Xuhai
collection PubMed
description The global “carbon emission peak” and “carbon neutrality” strategic goals promote us to replace current petroleum-based resin products with biomass-based resins. The use of technical lignins and hemicellulose-derived furfuryl alcohol in the production of biomass-based resins are among the most promising ways. Deep understanding of the resulting resin structure is a prerequisite for the optimization of biomass-based resins. Herein, a semiquantitative 2D HSQC NMR technique supplemented by the quantitative (31)P NMR and methoxyl group wet chemistry analysis were employed for the structural elucidation of softwood kraft lignin-based furfuryl alcohol resin (LFA). The LFA was fractionated into water-insoluble (LFA-I) and soluble (LFA-S) parts. The analysis of methoxyl groups showed that the amount of lignin was 85 wt% and 44 wt% in LFA-I and LFA-S fractions, respectively. The HSQC spectra revealed the high diversity of linkages formed between lignin and poly FA (pFA). The HSQC and (31)P results indicated the formation of new condensed structures, particularly at the 5-position of the aromatic ring. Esterification reactions between carboxyl groups of lignin and hydroxyl groups of pFA could also occur. Furthermore, it was suggested that lignin phenolic hydroxyl oxygen could attack an opened furan ring to form several aryl ethers structures. Therefore, the LFA resin was produced through crosslinking between lignin fragments and pFA chains.
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spelling pubmed-87461572022-01-11 Structural Analysis of Lignin-Based Furan Resin Zhu, Xuhai Bruijnaers, Bardo Lourençon, Tainise V. Balakshin, Mikhail Materials (Basel) Article The global “carbon emission peak” and “carbon neutrality” strategic goals promote us to replace current petroleum-based resin products with biomass-based resins. The use of technical lignins and hemicellulose-derived furfuryl alcohol in the production of biomass-based resins are among the most promising ways. Deep understanding of the resulting resin structure is a prerequisite for the optimization of biomass-based resins. Herein, a semiquantitative 2D HSQC NMR technique supplemented by the quantitative (31)P NMR and methoxyl group wet chemistry analysis were employed for the structural elucidation of softwood kraft lignin-based furfuryl alcohol resin (LFA). The LFA was fractionated into water-insoluble (LFA-I) and soluble (LFA-S) parts. The analysis of methoxyl groups showed that the amount of lignin was 85 wt% and 44 wt% in LFA-I and LFA-S fractions, respectively. The HSQC spectra revealed the high diversity of linkages formed between lignin and poly FA (pFA). The HSQC and (31)P results indicated the formation of new condensed structures, particularly at the 5-position of the aromatic ring. Esterification reactions between carboxyl groups of lignin and hydroxyl groups of pFA could also occur. Furthermore, it was suggested that lignin phenolic hydroxyl oxygen could attack an opened furan ring to form several aryl ethers structures. Therefore, the LFA resin was produced through crosslinking between lignin fragments and pFA chains. MDPI 2022-01-04 /pmc/articles/PMC8746157/ /pubmed/35009496 http://dx.doi.org/10.3390/ma15010350 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhu, Xuhai
Bruijnaers, Bardo
Lourençon, Tainise V.
Balakshin, Mikhail
Structural Analysis of Lignin-Based Furan Resin
title Structural Analysis of Lignin-Based Furan Resin
title_full Structural Analysis of Lignin-Based Furan Resin
title_fullStr Structural Analysis of Lignin-Based Furan Resin
title_full_unstemmed Structural Analysis of Lignin-Based Furan Resin
title_short Structural Analysis of Lignin-Based Furan Resin
title_sort structural analysis of lignin-based furan resin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746157/
https://www.ncbi.nlm.nih.gov/pubmed/35009496
http://dx.doi.org/10.3390/ma15010350
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