A Comparative Study of Lignin-Based Thermoset Properties: Mildly Extracted Organosolv Lignin versus Technical Kraft Lignin

Lignin is a highly abundant, renewable biopolymer with the potential to replace fossil-based aromatic building blocks in polymeric materials. However, the structural complexity of lignin, arising from its heterogeneous interunit linkages and irregular architecture, complicates the assessment of structure–property relationships. In this work, a lignin with a high content of the β-O-4′ interunit linkage, prevalent in native lignin, is utilized to reveal how the molecular structure governs the mechanical performance of lignin-based thermosets. The lignin was modified with allyl functionalities and thermally cross-linked using thiol–ene chemistry. A comprehensive structural analysis and characterization show that maintaining a high β-O-4′ content results in networks that exhibit both high modulus and ductile behavior (E: 1–3 GPa, and εb > 10%). This effectively addresses the trade-off between stiffness and ductility often encountered in technical lignin-based materials, having strain-at-break values below 4%. These findings highlight molecular structure as a crucial parameter for optimizing mechanical performance and tailoring lignin-based materials for high-performance applications, such as organic coatings or adhesives.

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Publication Details

Journal
ACS Sustainable Chemistry & Engineering
Published
2026-03-29
DOI
https://doi.org/10.1021/acssuschemeng.6c00236
Primary Topic
Lignin and Wood Chemistry
Type
article
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article

A Comparative Study of Lignin-Based Thermoset Properties: Mildly Extracted Organosolv Lignin versus Technical Kraft Lignin

Mats Johansson, Martin Lawoko, Louise Brandt, Benedikt Sochor et al.
ACS Sustainable Chemistry & Engineering
Lignin and Wood Chemistry
article

A Comparative Study of Lignin-Based Thermoset Properties: Mildly Extracted Organosolv Lignin versus Technical Kraft Lignin

Mats Johansson, Martin Lawoko, Louise Brandt, Benedikt Sochor, Constantin Harder, Alessio Truncali, Fika Andriani, Stephan Volkher Roth, Peter Müller-Buschbaum, Sarathlal K. Vayalil
article en

Abstract

Lignin is a highly abundant, renewable biopolymer with the potential to replace fossil-based aromatic building blocks in polymeric materials. However, the structural complexity of lignin, arising from its heterogeneous interunit linkages and irregular architecture, complicates the assessment of structure–property relationships. In this work, a lignin with a high content of the β-O-4′ interunit linkage, prevalent in native lignin, is utilized to reveal how the molecular structure governs the mechanical performance of lignin-based thermosets. The lignin was modified with allyl functionalities and thermally cross-linked using thiol–ene chemistry. A comprehensive structural analysis and characterization show that maintaining a high β-O-4′ content results in networks that exhibit both high modulus and ductile behavior (E: 1–3 GPa, and εb > 10%). This effectively addresses the trade-off between stiffness and ductility often encountered in technical lignin-based materials, having strain-at-break values below 4%. These findings highlight molecular structure as a crucial parameter for optimizing mechanical performance and tailoring lignin-based materials for high-performance applications, such as organic coatings or adhesives.

ACS Sustainable Chemistry & Engineering
Deutsches Elektronen-Synchrotron DESY (DE), Wallenberg Wood Science Center (SE), Technical University of Munich (DE), KTH Royal Institute of Technology (SE)
Openalex Percentile: Top 4%
Lignin and Wood Chemistry
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