Multifunctional graft-IPN hydrogels of cellulose nanofibers and poly(N-isopropyl acrylamide) via silver-promoted decarboxylative radical polymerization

Interpenetrating polymer networks (IPNs) have emerged as innovative materials for a wide range of applications. Owing to the crosslinked structure of their polymer components, IPNs exhibit superior properties relative to their single component counterparts. Here, we report a new class of multifunctional graft-interpenetrating polymer network (graft-IPN) hydrogel composites of poly(N-isopropylacrylamide) (PNIPAM) grafted onto cellulose nanofibers (CNFs) via silver(I)-promoted decarboxylative polymerization. This novel approach involves the Ag-promoted graft polymerization and the crosslinking of PNIPAM in the CNF network, forming a hybrid of semi-IPN and graft-copolymer hydrogel. Different from conventional PNIPAM-CNF IPNs, the CNFs in graft-IPN hydrogels form an interconnected network as a result of crosslinking between neighboring grafted PNIPAM. Silver nanoparticles (AgNPs) are also formed in situ in the graft-IPN hydrogel matrix, demonstrating the dual functionality of silver as both a catalyst in the polymerization and an eventual antibacterial agent in the hydrogel. The network structure of graft-IPN hydrogels can be controlled by crosslinker and Ag(I) concentration, therefore modulating their thermo-responsive, mechanical, and swelling properties. The grafting of PNIPAM from CNFs shifts the volume phase transition to 36 °C and significantly improves the mechanical strength and swelling capacity of the hydrogels. Ultimately, this work demonstrates the excellent potential of these multifunctional graft-IPN hydrogels with controllable thermosensitivity, mechanical strength and anti-microbial activity as engineered biomaterials for advanced applications in biomedicine, engineering, and industry.