Facile preparation of diformylxylose-derived adhesive for wood bonding

Wood-based panels like plywood alleviate the rapidly-growing global demand for timber, yet their production remains highly dependent on fossil-derived adhesives (e.g., urea-formaldehyde and phenol-formaldehyde resins) that impose considerable environmental and ecological concerns. As such, various renewable macromolecules such as lignin, starch, proteins, and hemicelluloses have been developed as bio-adhesives. However, the structural variability of these biomacromolecules, influenced by plant source and isolation methods, often leads to inconsistent adhesive performance during industrial scale-up. While adhesives synthesized from biomass-derived monomers can ensure better batch-to-batch uniformity, conventional refining systems (e.g., acidic and alkaline aqueous systems) still suffer from low efficiencies in isolating biomacromolecules from lignocelluloses and converting biomacromolecules into platform monomers (e.g., monosaccharides and furanics). Based on diformylxylose (DFX), a by-product derived from the acetal-protected lignocellulosic refining process, we herein report a novel DFX-derived bio-adhesive. This adhesive is prepared through two-step acid-catalyzed pre-reactions, i.e., pre-reaction I and II, followed by blending with a small amount of defatted soybean flour (DSF). After hot-pressing, it achieves both dry and wet bonding strengths of 1.4 MPa, significantly exceeding those of urea-formaldehyde resin as well as other sugar- (e.g., sucrose, starch and hemicelluloses) and protein-based (e.g., DSF) bio-adhesives. Additionally, residual formaldehyde molecules of pre-reaction I can be effectively captured by urea and additive (melamine or polyvinyl alcohol) in pre-reaction II, reducing the formaldehyde emission of three-layer plywood to as low as 0.58 mg/L. Characterizations indicate that the furanic prepolymers derived from pre-reaction I can undergo further covalent and non-covalent (e.g., hydrogen) cross-linking with additive (polyamine, or polyol) and DSF during pre-reaction II and hot-pressing, enhancing the cohesion and interfacial adhesion of DFX-derived bio-adhesives.

Authors

Publication Details

Journal
Industrial Crops and Products
Published
2026-01-15
DOI
https://doi.org/10.1016/j.indcrop.2026.122695
Primary Topic
Lignin and Wood Chemistry
Type
article
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article

Facile preparation of diformylxylose-derived adhesive for wood bonding

Xiaolin Luo, Ling Zhan, Guangshuai Zhao, Dalin Li et al.
Industrial Crops and Products
Lignin and Wood Chemistry
article

Facile preparation of diformylxylose-derived adhesive for wood bonding

Xiaolin Luo, Ling Zhan, Guangshuai Zhao, Dalin Li, Yi Ling, Jing Liu, Yangmei Chen
article en

Abstract

Wood-based panels like plywood alleviate the rapidly-growing global demand for timber, yet their production remains highly dependent on fossil-derived adhesives (e.g., urea-formaldehyde and phenol-formaldehyde resins) that impose considerable environmental and ecological concerns. As such, various renewable macromolecules such as lignin, starch, proteins, and hemicelluloses have been developed as bio-adhesives. However, the structural variability of these biomacromolecules, influenced by plant source and isolation methods, often leads to inconsistent adhesive performance during industrial scale-up. While adhesives synthesized from biomass-derived monomers can ensure better batch-to-batch uniformity, conventional refining systems (e.g., acidic and alkaline aqueous systems) still suffer from low efficiencies in isolating biomacromolecules from lignocelluloses and converting biomacromolecules into platform monomers (e.g., monosaccharides and furanics). Based on diformylxylose (DFX), a by-product derived from the acetal-protected lignocellulosic refining process, we herein report a novel DFX-derived bio-adhesive. This adhesive is prepared through two-step acid-catalyzed pre-reactions, i.e., pre-reaction I and II, followed by blending with a small amount of defatted soybean flour (DSF). After hot-pressing, it achieves both dry and wet bonding strengths of 1.4 MPa, significantly exceeding those of urea-formaldehyde resin as well as other sugar- (e.g., sucrose, starch and hemicelluloses) and protein-based (e.g., DSF) bio-adhesives. Additionally, residual formaldehyde molecules of pre-reaction I can be effectively captured by urea and additive (melamine or polyvinyl alcohol) in pre-reaction II, reducing the formaldehyde emission of three-layer plywood to as low as 0.58 mg/L. Characterizations indicate that the furanic prepolymers derived from pre-reaction I can undergo further covalent and non-covalent (e.g., hydrogen) cross-linking with additive (polyamine, or polyol) and DSF during pre-reaction II and hot-pressing, enhancing the cohesion and interfacial adhesion of DFX-derived bio-adhesives.

Industrial Crops and ProductsVol. 240
Responsible consumption and production
Openalex Percentile: Top 87%
Lignin and Wood Chemistry
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Facile preparation of diformylxylose-derived adhesive for wood bonding — Xiaolin Luo, Ling Zhan, et al. · Industrial Crops and Products (2026) | TGRS Research Map | TGRS