丙烯酰胺
纳米纤维
纤维素
自愈水凝胶
自由基聚合
高分子化学
材料科学
聚合
化学工程
单体
化学
聚合物
有机化学
复合材料
工程类
作者
David Joram Mendoza,Naghmeh Nasiri,Rebekah N. Duffin,Vikram Singh Raghuwanshi,Jitendra Mata,George P. Simon,Joel F. Hooper,Gil Garnier
标识
DOI:10.1016/j.mtchem.2024.102014
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI