4.7 Article

Influence of delignification on plastic flow deformation of wood

Journal

CELLULOSE
Volume 29, Issue 7, Pages 4153-4165

Publisher

SPRINGER
DOI: 10.1007/s10570-022-04555-0

Keywords

Wood; Plastic deformation; Deformability; Delignification; NMR

Funding

  1. Asahi Kasei Corporation

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This study investigates the influence of delignification on the plastic flow deformation of wood, and evaluates the effects of lignin's chemical structure, distribution, and molecular motility on wood deformability. The results show that delignified wood undergoes significant deformation at lower pressure without cell wall destruction. The deformability of wood increases with temperature and improves significantly as lignin near the polysaccharides in the cell wall is removed. The correlation between chemical and physicochemical properties and plastic flow deformability presented in this study is important for low-energy and highly productive formation of solid-state wood.
In this study, we elucidated the influence of delignification of wood on its plastic flow deformation caused by the shear sliding of wood cells. The delignified wood samples were characterized by attenuated total reflection-infrared (ATR-IR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, Raman imaging analysis, and dynamic viscoelastic measurements. Then, the effects of the chemical structure, distribution, and molecular motility of lignin on the deformability of wood were evaluated. The delignified wood in water-swollen state was significantly deformed without cell wall destruction at a lower pressure than the untreated wood. The deformability was evaluated from two perspectives: stress at flow starting point and deformed cross-sectional area of the wood sample. The deformability of the delignified and untreated wood increased with increasing temperature during compression. In the early stages of delignification, the lignin in the compound middle lamella decreased, especially at the cell corner, which reduced the stress at the flow starting point. However, the deformed cross-sectional area of wood varied slightly with delignification time in these stages. As the delignification proceeded, the lignin at the vicinity of the polysaccharides in the cell wall was removed and the deformability improved significantly. Additionally, the stress at the flow starting point increased linearly with the peak temperature of tan delta, corresponding to the glass transition temperature of lignin in water-swollen wood, regardless of the temperature during compression. The correlation between chemical and physicochemical properties and plastic flow deformability presented in this paper will aid in low-energy and highly productive formation of solid-state wood.

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