Multiscale mechanical properties and enhancement mechanism of cellulose-composited hydrogels
Na Li, Shaojun Qi, Laura Buccoli, Pablo Del Pozo Lorenzale, Roxana Guillén De La Cruz, Adrian L. Harris, Zhenyu J. Zhang
Abstract
We prepared cellulose-composited ionic-covalent entanglement (ICE) network gelatin methacrylate/alginate (G/A) hydrogels using microfibrillated cellulose (MFC) and nanofibrillated cellulose (NFC), of which the mechanical properties were evaluated at two different length scales. Macro-compression shows that cellulose improves the toughness, compression resistance, and Young's moduli of ICE hydrogels, attributed to the synergistic interaction between the cellulose fiber network and ICE due to hydrogen bonding. Pure MFC (363.43 kPa) or NFC (325.75 kPa) alone, compared to a blend of the two with varied contents (261.5-288.5 kPa), displays a more pronounced improvement in the Young's moduli of ICE hydrogels, because homogeneous fiber networks enhance the structural integrity of the system. Micro-indentation reveals that hydrogen bonds between cellulose and ICE weaken the time-dependent deformation of cellulose-composited ICE hydrogel. Mapping of Young's modulus and hardness distribution of the hydrogel suggests that there are three forms of enhancement within cellulose-composited ICE hydrogel: cellulose fiber networks, ICE synergistic network, and synergies between cellulose fiber network and ICE. Creep results highlight that the excellent confinement effect of MFC contributes to creep resistance of cellulose-composited ICE hydrogels. In conclusion, the multiscale characterization unravels the mechanical reinforcing mechanisms of cellulose fibres in ICE hydrogels, which demonstrates the possible strategies for improving the mechanical properties of hydrogels.