Self-Healing of Polymers via Supramolecular Chemistry

被引：151
|
作者：
Yang, Ying [1 ]
Urban, Marek W. [1 ]
机构：
[1] Clemson Univ, COMSET, Dept Mat Sci & Engn, Clemson, SC 29634 USA
来源：
ADVANCED MATERIALS INTERFACES | 2018年 / 5卷 / 17期
基金：
美国国家科学基金会;
关键词：
self-healing polymers; supramolecular chemistry; PI-PI STACKING; HOST-GUEST; CROWN-ETHER; POLYURETHANE NETWORKS; REVERSIBLE POLYMERS; BLOCK-COPOLYMERS; IONIC LIQUIDS; HYDROGELS; GELS; COVALENT;
D O I：
10.1002/admi.201800384
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Recent advances of supramolecular chemistry utilized in the development of self-healing polymers have revealed that the rate and equilibrium constants of bond dissociation/re-association, bonding directionality, chain relaxation time, decay rate of chain relaxation after damage, and cluster formation may impact the healing efficiency in a given environment. This review provides an assessment of supramolecular chemistries responsible for self-healing using H-bonding, metal-ligand, host-guest, ionic, pi-pi, and hydrophobic interactions. The impact of these chemistries on self-healing is examined for various polymeric systems with multifunctional applications which are unique to supramolecular networks. This review also discusses the driving forces leading to physical damage closure in the context of supramolecular bond dynamics, providing insights into the design principles to achieve efficient recovery.
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页数：19
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