A Lignin‐Based Phenolic Resin With a Rapid Curing Rate and High Bonding Strength

ABSTRACT Inspired by the adhesive mechanism of mussel adhesive protein (DOPA), lignin was oxidized under mild conditions to mimic catechol and ortho‐quinone structures. The resulting oxidized lignin (ODL) was subsequently employed to prepare fast‐curing lignin‐based phenolic resins (ODLPF). Structural characterizations confirmed that the phenolic rings in lignin were transformed into ortho‐quinone and/or catechol following the oxidation reaction. The reactive functional groups in ODL facilitated cross‐linking reactions with the phenolic resin networks, while catechol underwent a reverse dismutation reaction with ortho‐quinone. The ODLPF resins demonstrated enhanced performance, including a faster curing rate, improved bonding strength, higher debonding work, and superior thermal stability compared to unmodified lignin‐based phenolic resins. This biomimetic modification strategy offers a sustainable approach to developing high‐performance biomass‐based phenolic resins with significant potential for industrial applications.

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Publication Details

Journal
Polymer Engineering and Science
Published
2025-12-23
DOI
https://doi.org/10.1002/pen.70314
Primary Topic
Lignin and Wood Chemistry
Type
article
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article

A Lignin‐Based Phenolic Resin With a Rapid Curing Rate and High Bonding Strength

Jiongjiong Li, Yan Lyu, Xiaona Li, Jin Wang et al.
Polymer Engineering and Science
Lignin and Wood Chemistry
article

A Lignin‐Based Phenolic Resin With a Rapid Curing Rate and High Bonding Strength

Jiongjiong Li, Yan Lyu, Xiaona Li, Jin Wang, Xiaobin Yu, Zhiqin Wang, Jianzhang Li
article en

Abstract

ABSTRACT Inspired by the adhesive mechanism of mussel adhesive protein (DOPA), lignin was oxidized under mild conditions to mimic catechol and ortho‐quinone structures. The resulting oxidized lignin (ODL) was subsequently employed to prepare fast‐curing lignin‐based phenolic resins (ODLPF). Structural characterizations confirmed that the phenolic rings in lignin were transformed into ortho‐quinone and/or catechol following the oxidation reaction. The reactive functional groups in ODL facilitated cross‐linking reactions with the phenolic resin networks, while catechol underwent a reverse dismutation reaction with ortho‐quinone. The ODLPF resins demonstrated enhanced performance, including a faster curing rate, improved bonding strength, higher debonding work, and superior thermal stability compared to unmodified lignin‐based phenolic resins. This biomimetic modification strategy offers a sustainable approach to developing high‐performance biomass‐based phenolic resins with significant potential for industrial applications.

Polymer Engineering and ScienceVol. 66(3)
Nanjing Forestry University (CN), Yantai University (CN), Beijing Forestry University (CN), Institute of Chemical Industry of Forest Products (CN), Kingdee (China) (CN)
Industry, innovation and infrastructure
Openalex Percentile: Top 43%
Lignin and Wood Chemistry
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