结晶
材料科学
六亚甲基二异氰酸酯
成核
纳米复合材料
极限抗拉强度
复合材料
纤维素
纳米晶
化学工程
纳米技术
化学
聚氨酯
有机化学
工程类
作者
Ling Yan,Gaojun Lu,Somia Yassin Hussain Abdalkarim,Lunhe Wang,Zhiming Chen,Weidong Lu,Hou‐Yong Yu
标识
DOI:10.1016/j.ijbiomac.2023.128264
摘要
The slow crystallization and weak mechanical features of poly (butylene adipate-co-terephthalate) (PBAT) have become a severe industrial problem in food packaging. Inspired by principle of bionic structure, functional cellulose nanocrystals (CNC) modified with hexamethylene diisocyanate (HMDI) and toluene diisocyanate (TDI) can enhance the crystallization ability and mechanical properties of PBAT nanocomposites. Significantly, CNC-T (CNC modified by TDI) showed a stronger reinforced effect on PBAT properties than unmodified CNCs and CNC-H (CNC modified by HMDI) nanofillers due to hydrogen bonds, π-π interaction between PBAT matrix and CNC-T nanofillers with benzene ring structure. Thus, compared with pure PBAT, PBAT/5CNC-T composites displayed an enhancement of 34.5 % on the tensile strength and exhibited the most robust nucleation ability on PBAT crystallization than CNC and CNC-H. Meanwhile, the possible nucleation, crystallization, and performance reinforcement mechanisms of PBAT nanocomposites have been presented, which is very beneficial for designing robust PBAT nanocomposites with functional cellulose nanocrystals for potential green packaging.
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