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Impact of lignin source on the performance of thermoset resins

[Display omitted] •Hardwood lignin-based resins with different mechanical properties were prepared.•The lignin fractions were highly functionalized by using diallyl carbonate.•The 50% of the thiol conversion was reached in less than 3 h (except for one fraction).•Sandwich and T-shaped π-π stacking i...

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Published in:European polymer journal 2023-07, Vol.194, p.112141, Article 112141
Main Authors: Ribca, Iuliana, Sochor, Benedikt, Betker, Marie, Roth, Stephan V., Lawoko, Martin, Sevastyanova, Olena, Meier, Michael A.R., Johansson, Mats
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container_title European polymer journal
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creator Ribca, Iuliana
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description [Display omitted] •Hardwood lignin-based resins with different mechanical properties were prepared.•The lignin fractions were highly functionalized by using diallyl carbonate.•The 50% of the thiol conversion was reached in less than 3 h (except for one fraction).•Sandwich and T-shaped π-π stacking interactions were identified in all lignin samples. A series of different technical hardwood lignin-based resins have been successfully synthesized, characterized, and utilised to produce thiol-ene thermoset polymers. Firstly, technical lignin was fractionated and allylated, whereafter it was crosslinked with a trifunctional thiol. Structural and morphological characteristics of the lignin fractions were studied by 1H NMR, 31P NMR, SEC, FTIR, DSC, TGA, and WAXS. The hardwood lignin fractions have a high content of C5-substituted OH groups. The WAXS studies on lignin fractions revealed the presence of two π-π stacking conformations, sandwiched (4.08–4.25 Å) and T-shaped (6.52–6.91 Å). The presence of lignin superstructures with distances/sizes between 10.5 and 12.8 Å was also identified. The curing reaction of the thermosets was investigated by RT-FTIR. Almost all thermosets (excepting one fraction) reached 95% of the thiol conversion in less than 17 h, revealing the enhanced reactivity of the allylated hardwood lignin samples. The mechanical properties of the thermosets were investigated by DMA. The curing performance, as well as the final thermoset properties, have been correlated to variations in chemical composition and morphological differences of lignin fractions. The described results clearly demonstrate that technical hardwood lignins can be utilized for these applications, but also that significant differences compared to softwood lignins have to be considered for material design.
doi_str_mv 10.1016/j.eurpolymj.2023.112141
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A series of different technical hardwood lignin-based resins have been successfully synthesized, characterized, and utilised to produce thiol-ene thermoset polymers. Firstly, technical lignin was fractionated and allylated, whereafter it was crosslinked with a trifunctional thiol. Structural and morphological characteristics of the lignin fractions were studied by 1H NMR, 31P NMR, SEC, FTIR, DSC, TGA, and WAXS. The hardwood lignin fractions have a high content of C5-substituted OH groups. The WAXS studies on lignin fractions revealed the presence of two π-π stacking conformations, sandwiched (4.08–4.25 Å) and T-shaped (6.52–6.91 Å). The presence of lignin superstructures with distances/sizes between 10.5 and 12.8 Å was also identified. The curing reaction of the thermosets was investigated by RT-FTIR. Almost all thermosets (excepting one fraction) reached 95% of the thiol conversion in less than 17 h, revealing the enhanced reactivity of the allylated hardwood lignin samples. The mechanical properties of the thermosets were investigated by DMA. The curing performance, as well as the final thermoset properties, have been correlated to variations in chemical composition and morphological differences of lignin fractions. 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subjects Allylation
Chemistry
Hardwood lignin
Kemi
Solvent fractionation
Thiol-ene thermosets
Wide-angle X-ray scattering
π-π stacking interactions
title Impact of lignin source on the performance of thermoset resins
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