High strength, self-healing polyurethane elastomer based on synergistic multiple dynamic interactions in multiphase

被引:7
|
作者
Liu, Dan [1 ]
Fan, Cheng-Jie [1 ,2 ]
Xiao, Yi [1 ]
Yang, Ke-Ke [1 ]
Wang, Yu-Zhong [1 ]
机构
[1] Sichuan Univ, Coll Chem, Collaborat Innovat Ctr Ecofriendly & Fire Safety P, State Key Lab Polymer Mat Engn,Natl Engn Lab Ecofr, Chengdu 610064, Peoples R China
[2] Chengdu Shishi High Sch, Chengdu 610052, Sichuan, Peoples R China
关键词
DISULFIDE; BONDS; GELATINIZATION; NETWORKS; STARCH;
D O I
10.1016/j.polymer.2022.125513
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Inspired by some biological phenomena, self-healing materials has been made great progress over the past decades. However, it is challenging to establish an adaptable strategy to achieve a good tradeoff between mechanical strength and self-healing ability. Herein, we reported a self-healing polyurethane elastomer (PPG-UPy-SS) with desirable mechanical performance and wonderful self-healing capacity via incorporating synergistic multiple dynamic interactions in multiphase. The 2-amino-5-(2-hydroxyethyl)-6-methylpyrimidin-4-ol (UPy) motif was introduced into the PPG segment to keep the mechanical performance profiting from the regular arrangement of hydrogen-bonding array and microphase separation benefited from 7C-7C stacking of UPy dimers. 4-aminophenyl disulfide (APDS) was embedded into the loosely stacked amorphous region to increase the mobility of the chain segment to improve self-healing performance. The optimized sample PPG-UPy50%-SS50% possesses high tensile strength and fracture toughness of 18.2 MPa and 57.3 MJ m- 3, and satisfactory self-healing efficiency of 99% and 96% (10 h at 80 ?), respectively.
引用
收藏
页数:7
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