Synthesis, self-assembly and self-healing properties of organic-inorganic ABA triblock copolymers with poly(POSS acrylate) endblocks

被引:16
作者
Zhao, Bingjie [1 ,2 ]
Xu, Sen [1 ,2 ]
Zheng, Sixun [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Polymer Sci & Engn, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
关键词
TRANSFER RADICAL POLYMERIZATION; BLOCK-COPOLYMERS; SHAPE-MEMORY; LINEAR VISCOELASTICITY; HYBRID POLYMERS; PHASE-BEHAVIOR; MORPHOLOGIES; NANOCOMPOSITES; METHACRYLATE; SOLVENTS;
D O I
10.1039/c9py00094a
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A novel organic-inorganic ABA triblock copolymer with a poly(acrylate amide) (PAA) midblock and poly (POSS acrylate) [ P(POSS)] endblocks was synthesized via sequential reversible addition-fragmentation chain transfer (RAFT) polymerization. The triblock copolymers displayed self-assembly behavior in aqueous solutions; the spherical nanoobjects were formed in aqueous dispersions. Small angle X-ray scattering (SAXS) and transmission electron microscopy (TEM) showed that the triblock copolymers were microphase-separated; the P(POSS) blocks were self-organized into the microdomains dispersed in a PAA matrix. The PAA matrix was significantly reinforced by the P(POSS) microdomains, which was evidenced by the fact that the organic-inorganic triblock copolymers possessed improved thermomechanical properties. In addition, the triblock copolymers can display self-healing properties. It is proposed that in the microphase-separated triblock copolymers, the dynamic exchange of hydrogen bonds in the continuous elastomeric matrix (viz. PAA) is responsible for the rehealable ability whereas the P(POSS) microdomains imparted the improved mechanical properties to the materials.
引用
收藏
页码:2424 / 2435
页数:12
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