Fabricating a fully lignin-based adhesive from in-situ phenolation of lignocellulosic biomass

Lignin, as the main by-product from the chemical pulping process, has suffered serious structural damage, resulting in increased condensation and reduced activity, which makes it difficult to realize high-valued applications. Herein, we proposed a facile strategy for preparing fully lignin-based adhesive directly from lignocellulosic biomass via in-situ phenolation. The in-situ phenolation that occurred during the delignification process endowed the extracted lignin with numerous phenolic hydroxyl groups, enabling the highly reactive lignin to possess the possibility as a natural lignin-based wood adhesive. The process of fabricating the lignin-based adhesive could be achieved via a simple mixing of the in-situ phenolated lignin and alkali lignin in basic solution. The plywood products prepared with the lignin-based adhesive exhibited superior performance with dry and wet bonding strengths reaching 3.09 MPa and 0.92 MPa, respectively. Mechanistic analysis revealed that hot pressing induced lignin self-polymerization and formation of new ether linkages, contributing to the enhanced adhesion. Compared with reported lignin-based adhesive systems, this aldehyde-free formulation achieved competitive bonding performance without aldehyde-based crosslinkers, indicating its potential as a sustainable alternative to formaldehyde-based wood adhesives. This work presents a facile strategy for producing fully lignin-based adhesives from biomass and provides insight into formaldehyde-free wood adhesive systems.

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Publication Details

Journal
Advanced Composites and Hybrid Materials
Published
2026-05-29
DOI
https://doi.org/10.1007/s42114-026-01884-7
Primary Topic
Lignin and Wood Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Fabricating a fully lignin-based adhesive from in-situ phenolation of lignocellulosic biomass

Pedram Fatehi, Sai Hu, Yingjuan Fu, Ruijie Wu et al.
Advanced Composites and Hybrid Materials
Lignin and Wood Chemistry
article

Fabricating a fully lignin-based adhesive from in-situ phenolation of lignocellulosic biomass

Pedram Fatehi, Sai Hu, Yingjuan Fu, Ruijie Wu, Chunlin Xu, Yongchao Zhang, Xiaodi Wang
article en

Abstract

Lignin, as the main by-product from the chemical pulping process, has suffered serious structural damage, resulting in increased condensation and reduced activity, which makes it difficult to realize high-valued applications. Herein, we proposed a facile strategy for preparing fully lignin-based adhesive directly from lignocellulosic biomass via in-situ phenolation. The in-situ phenolation that occurred during the delignification process endowed the extracted lignin with numerous phenolic hydroxyl groups, enabling the highly reactive lignin to possess the possibility as a natural lignin-based wood adhesive. The process of fabricating the lignin-based adhesive could be achieved via a simple mixing of the in-situ phenolated lignin and alkali lignin in basic solution. The plywood products prepared with the lignin-based adhesive exhibited superior performance with dry and wet bonding strengths reaching 3.09 MPa and 0.92 MPa, respectively. Mechanistic analysis revealed that hot pressing induced lignin self-polymerization and formation of new ether linkages, contributing to the enhanced adhesion. Compared with reported lignin-based adhesive systems, this aldehyde-free formulation achieved competitive bonding performance without aldehyde-based crosslinkers, indicating its potential as a sustainable alternative to formaldehyde-based wood adhesives. This work presents a facile strategy for producing fully lignin-based adhesives from biomass and provides insight into formaldehyde-free wood adhesive systems.

Advanced Composites and Hybrid Materials
Åbo Akademi University (FI), Qilu University of Technology (CN), Taishan University (CN), Lakehead University (CA)
National Natural Science Foundation of China
Responsible consumption and production
Openalex Percentile: Top 10%
Lignin and Wood Chemistry
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