Its excellent renewability and biodegradability make
cellulose
an attractive resource to prepare fossil-based plastic alternatives.
However, cellulose itself exhibits strong intermolecular hydrogen
bond (H-bond) interactions, significantly restricting the mobility
of cellulose chains, thus leading to poor thermo-processing performance.
Here, we reconstructed the intermolecular interactions of cellulose
chains via replacing the original H-bonds with dynamic covalent bonds.
By this, cellulose can be easily thermo-processed into a cellulosic
plastic under mild conditions (70 °C). Through adjusting the
chemical structure of dynamic covalent networks, the cellulosic plastic
shows tunable mechanical strength (3.0–33.5 MPa) and toughness
(43–321 kJ m–2). The cellulosic plastic also
exhibits excellent resistance to water, organic solvent, acid solution,
alkali solution, and high temperature (>400 °C). Moreover,
it
owns good chemical and biological degradability and recyclability.
This work provides an effective method to develop high-performance
cellulosic plastics for fossil-based plastic substitution.