A bio-based route to formaldehyde-free, wet-durable wood bonding: aldehyde-functionalized straw microparticles stabilize networks and interphases in polyacrylamide adhesives

Abstract

Polyacrylamide (PAM) can offer strong dry wood adhesion via amide-wood hydrogen bonding but typically fails in water due to severe network swelling. Here we report a reinforcing approach using aldehyde-functionalized straw microparticles (AFstraw) as a multifunctional reactive lignocellulosic component. AFstraw was prepared via periodate-mediated aldehydation and dispersed into an aqueous bio-synthesized acrylamide (bio-AM) precursor before curing. Compared with neat PAM that shows no measurable wet strength, PAM/AFstraw enables a step-change in wet durability while preserving excellent dry bonding. Optimal processing formulation delivers up to 1.73 MPa wet strength after 63 °C water soaking, well above the commonly referenced 0.7 MPa criterion. Microscopy collectively reveals a more adhesive-rich bondline, consistent with stabilization of the wood-adhesive interphase. FTIR indicates aldehyde consumption, while swelling tests support adhesive-network stabilization in water (31% vs. 530% for neat PAM). A cradle-to-gate LCA indicates a low GWP (2.44 kg CO2-eq kg-1 adhesive) and lower modeled toxicity-related potentials relative to several mainstream resins, while identifying sodium periodate and electricity as dominant hotspots. Overall, this work demonstrates an aldehyde-enabled strategy that uses lignocellulosic microparticles to unlock PAM’s adhesive potential, opening possibilities toward sustainable wood composite manufacturing.

Supplementary files

Article information

Article type
Paper
Submitted
20 Mar 2026
Accepted
19 Jun 2026
First published
22 Jun 2026

Green Chem., 2026, Accepted Manuscript

A bio-based route to formaldehyde-free, wet-durable wood bonding: aldehyde-functionalized straw microparticles stabilize networks and interphases in polyacrylamide adhesives

B. Hu, F. Gao, Y. Xu, K. Zhang, M. Qiang, J. Xu, L. Qiu and H. Chen, Green Chem., 2026, Accepted Manuscript , DOI: 10.1039/D6GC01686C

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