Regulation of mechanical properties and self-healing performance of polyurethane nanocomposites by tuning the contents of free and associated hydrogen bonds

被引:9
作者
Zhang, Aofei [1 ]
Huang, Qiaona [1 ]
Du, Xiaoyu [1 ]
Wang, Yinmao [2 ]
Yang, Juan [1 ]
Li, Sumin [1 ]
Zhu, Maiyong [1 ]
Nie, Yijing [1 ]
机构
[1] Jiangsu Univ, Res Sch Polymer Mat, Sch Mat Sci & Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Tiemao Glass Co Ltd, Key Lab High Performance Transparent Protect Mat J, Nantong 226600, Peoples R China
基金
中国国家自然科学基金;
关键词
WATERBORNE POLYURETHANE; COMBINATION; POLYMERS; RUBBER; ELASTOMERS; NETWORKS;
D O I
10.1039/d3py01098h
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Hydrogen bonds facilitate self-healing of polymers. However, free and associated hydrogen bonds have different effects on mechanical properties and self-healing performance. Here, both unmodified nano-silica (nano-SiO2) and nano-SiO2 modified by 2-ureido-4[1H]-pyrimidinone (UPy) and KH-550 (UK-SiO2) were used to fill polyurethane (PU). The mechanical properties and self-healing properties of the PU nanocomposites can be regulated by changing the ratio of the two kinds of nano-SiO2. In the PU containing 2 wt% unmodified nano-SiO2 and 1 wt% UK-SiO2, the UK-SiO2 particles hinder the agglomeration of the unmodified nano-SiO2 particles and facilitate the formation of hydrogen bonds between PU chains and the nanofillers. More associated hydrogen bonds exist, resulting in a higher mechanical strength but a weaker self-healing ability. In the PU containing more UK-SiO2, the formation of hydrogen bonds between the unmodified nano-SiO2 particles and between the unmodified nano-SiO2 particles and PU chains is restricted by the UK-SiO2 particles, leading to a lower mechanical strength but a stronger self-healing ability. The mechanical properties and self-healing efficiency of PU/SiO2 nanocomposites can be tuned by changing the contents of free and associated hydrogen bonds.
引用
收藏
页码:384 / 396
页数:13
相关论文
共 56 条
[21]   An intermolecular quadruple hydrogen-bonding strategy to fabricate self-healing and highly deformable polyurethane hydrogels [J].
Lin, Yinlei ;
Li, Guangji .
JOURNAL OF MATERIALS CHEMISTRY B, 2014, 2 (39) :6878-6885
[22]   An advanced elastomer with an unprecedented combination of excellent mechanical properties and high self-healing capability [J].
Liu, Jie ;
Liu, Jun ;
Wang, Sheng ;
Huang, Jing ;
Wu, Siwu ;
Tang, Zhenghai ;
Guo, Baochun ;
Zhang, Liqun .
JOURNAL OF MATERIALS CHEMISTRY A, 2017, 5 (48) :25660-25671
[23]   Design of Self-Healing Rubber by Introducing Ionic Interaction To Construct a Network Composed of Ionic and Covalent Cross-Linking [J].
Liu, Yong ;
Li, Zhaolei ;
Liu, Rongjuan ;
Liang, Zhaopeng ;
Yang, Jun ;
Zhang, Ruilong ;
Zhou, Zhiping ;
Nie, Yijing .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2019, 58 (32) :14848-14858
[24]  
Luo C., 2010, J FUYANG TEACH COLL, V27, P1
[25]   Toughening diene elastomers by strong hydrogen bond interactions [J].
Luo, Ming-Chao ;
Zeng, Jian ;
Fu, Xuan ;
Huang, Guangsu ;
Wu, Jinrong .
POLYMER, 2016, 106 :21-28
[26]   A Highly Stretchable and Autonomous Self-Healing Polymer Based on Combination of Pt•••Pt and π-π Interactions [J].
Mei, Jin-Feng ;
Jia, Xiao-Yong ;
Lai, Jian-Cheng ;
Sun, Yang ;
Li, Cheng-Hui ;
Wu, Jun-Hua ;
Cao, Yi ;
You, Xiao-Zeng ;
Bao, Zhenan .
MACROMOLECULAR RAPID COMMUNICATIONS, 2016, 37 (20) :1667-1675
[27]   New insights into thermodynamic description of strain-induced crystallization of peroxide cross-linked natural rubber filled with clay by tube model [J].
Nie, Yijing ;
Huang, Guangsu ;
Qu, Liangliang ;
Wang, Xiaoan ;
Weng, Gengsheng ;
Wu, Jinrong .
POLYMER, 2011, 52 (14) :3234-3242
[28]   Wearable electronics [J].
Peng, Huisheng .
NATIONAL SCIENCE REVIEW, 2023, 10 (01)
[29]   POLYURETHANE ELASTOMERS [J].
PETROVIC, ZS ;
FERGUSON, J .
PROGRESS IN POLYMER SCIENCE, 1991, 16 (05) :695-836
[30]   Double Reversible Networks: Improvement of Self-Healing in Hybrid Materials via Combination of Diels-Alder Cross-Linking and Hydrogen Bonds [J].
Schaefer, Sandra ;
Kickelbick, Guido .
MACROMOLECULES, 2018, 51 (15) :6099-6110