纳米复合材料
明胶
材料科学
化学工程
石墨烯
原位聚合
热稳定性
极限抗拉强度
纤维素
氧化物
复合材料
聚合
聚合物
纳米技术
化学
有机化学
工程类
冶金
作者
Li Kuang,Shicun Jin,Jianzhang Li,Hui Chen
标识
DOI:10.1016/j.indcrop.2019.02.011
摘要
Inspired by the natural mussel chemical engineering, we proposed a novel and biomimetic strategy for the fabrication of strong integrated gelatin/cellulose nanofibrils (CNF) nanocomposite materials reinforced with functional graphene oxide (GO) nanohybrids. GO nanosheets were chemically reduced and dip-coated to yield poly(dopamine) (PDA)-functionalized GO (PGO) via self-polymerization of catechol-containing dopamine. Furthermore, Ag nanoparticles (NPs) were further prepared and immobilized by the catechol groups of the functional PDA layers through in-situ reduction and strong catechol-metal interaction. The fracture surface morphology clearly revealed that the interfacial adhesion of gelatin-based nanocomposite was remarkably improved via the synergistic effect and multiple cross-linking interactions of the CNF-PGO nanohybrids and Ag NPs. The tensile strength and toughness of the nanocomposite film were simultaneously increased to 35.99 MPa and 13.49 MJ/m3, respectively. The water vapor permeability of the nanocomposite was remarkably reduced by 51.60%. The nanocomposite film showed strong antibacterial activity against both S. aureus and E. coli pathogenic bacteria. In addition, the film also exhibited significant improvement in the water resistance, UV-shielding capacity, and thermal stability. Hence, the bio-inspired strategy for constructing functional PGO nanohybrids in renewable natural gelatin/CNF nanocomposites provides a promising approach to the fabrication of active packaging materials for a wide range of industrial applications.
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