Issue 2, 2024

Hydrodeoxygenation of condensed lignins followed by acid-mediated methylolation enables preparation of lignin-based wood adhesives

Abstract

Lignin is a phenolic polymer, making it a sustainable alternative to phenol for synthesizing lignin–phenol–formaldehyde (LPF) adhesives. However, technical lignins produced in pulping or biorefining processes are generally highly condensed and have low reactivity, limiting their uses in synthesizing phenolic-based adhesives. Herein, we report a two-step strategy to produce lignin-based wood adhesives with industrially available technical lignins through hydrodeoxygenation followed by acid-mediated methylolation of aromatic C2/6 positions to improve the flowability, water resistance, and crosslinking ability of lignins. We demonstrated that this biobased lignin–formaldehyde adhesive had a lighter color and far better adhesion performance compared to traditional LPF resins prepared from base-mediated methylolation of lignins. Mechanistic investigation suggests that the chemical crosslinking of methylolated lignin to form diarylmethane structures and the physical interlocking interaction at the interfaces of wood veneers contribute to the strength of plywood.

Graphical abstract: Hydrodeoxygenation of condensed lignins followed by acid-mediated methylolation enables preparation of lignin-based wood adhesives

Supplementary files

Article information

Article type
Communication
Submitted
16 10月 2023
Accepted
10 11月 2023
First published
11 11月 2023

Green Chem., 2024,26, 753-759

Hydrodeoxygenation of condensed lignins followed by acid-mediated methylolation enables preparation of lignin-based wood adhesives

G. Yang, Z. Gong, B. Zhou, X. Luo, J. Liu, G. Du, C. Zhao and L. Shuai, Green Chem., 2024, 26, 753 DOI: 10.1039/D3GC03935H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements