Effect of lignin on the self-bonding of a natural fiber material in a hydrothermal environment: Lignin structure and characterization

Abstract

Self-bonding natural fiber materials (SNFMs) were prepared at different initial moisture contents (IMCs) through a molding pressing process. The self-bonding mechanism of the SNFMs was deduced from the chemical and structural changes of lignin and their mechanical strengths. The structural transformations of milled wood lignin (MWL) in the SNFMs were investigated by two-dimensional heteronuclear single quantum coherence, quantitative 31P-nuclear magnetic resonance spectra, gelpermeation chromatography, and thermogravimetric analysis. As IMC increased from 0% to 80%, the tensile strength increased from 23.0 to 70.0 MPa and the density increased from 0.99 to 1.05 g/cm3. IMC affected the distribution and abundance of the typical lignin linkages (β-O-4′, β-β, and β-5′) and the S–OH/G–OH ratios of lignin. Moreover, as IMC increased, the aliphatic hydroxyl groups proportionally decreased, while the condensed phenolic and non-condensed phenolic hydroxyl groups increased, the molecular weight of MWL became larger, and the thermal stability of lignin improved. These findings indicate the simultaneous occurrence of depolymerization and condensation reactions of lignin. The condensation reaction dominated, improving the mechanical strength of the material. Our results explain (at least partly) the self-bonding mechanism of SNFMs.