Monitoring crystallite fusion of nanocellulose during colloid condensation

Abstract

The crystallinity of cellulose decreases when bundled microfibrils are dispersed in water as cellulose nanofibers (CNFs) or physically separated into finer nanoscale fibrils or single microfibrils. The crystallinity of these CNFs is recovered when they become densely assembled through the dehydration of the dispersion. In this process, multiple CNFs are assumed to partially fuse, leading to the enlargement of crystallite widths. The mechanism of this CNF fusion is, however, not well understood. In this study, the recovery process of the crystallinity of CNFs was monitored by sampling wet CNF gels during condensation from a dilute dispersion to a dense aggregate, followed by wide-angle X-ray diffractometry (WAXD) and solid-state 13C nuclear magnetic resonance (NMR) spectroscopy analyses after supercritical drying. In the WAXD analysis, a two-step enlargement in the (2 0 0) crystal size was observed: the first step was a rapid increase in the range of solid content up to 1%, followed by a gradual increase in the range of 1–85%. The crystallinity index estimated by NMR hardly changed in the range of 0.5–30% but gradually increased in the range of 30–85%. A portion of the CNF samples, without drying, were also subjected to small-angle X-ray scattering and viscoelasticity analyses, indicating that the inter-CNF contact points in water significantly increased until reaching a solid content of 1%, and then at solid contents higher than 1%, the contact areas of each point gradually expanded. Finally, a mechanism of CNF fusion was proposed based on these results.