共 50 条
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
来源:
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.
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页数:7
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