Influence of soft block and film thickness on confined morphology of poly(ether-mb-amide) multiblock copolymers

被引:9
|
作者
Cao, Yiyu [1 ,2 ,3 ]
Zhu, Ping [1 ]
Zhou, Yong [1 ]
Wang, Dujin [1 ,2 ]
Dong, Xia [1 ,2 ]
机构
[1] Chinese Acad Sci, CAS Res Educ Ctr Excellence Mol Sci, Inst Chem, CAS Key Lab Engn Plast,Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, Polymers & Composites Div, Key Lab Biobased Polymer Mat Technol & Applicat Z, Ningbo, Peoples R China
关键词
confined morphology; crystallization behavior; film thickness; poly(ether-mb-amide) multiblock copolymers; POLYMER CRYSTALLIZATION; ULTRATHIN FILMS; CRYSTAL-GROWTH; THIN-FILMS; QUASI-2; DIMENSIONS; TEMPERATURE; BULK; POLYURETHANES; ORIENTATIONS; POLYSTYRENE;
D O I
10.1002/pcr2.10100
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
This work investigated the confined morphology within ultrathin films of a family of poly(ether-mb-amide) multiblock copolymer (PEAc) samples, which contains longchain carbon polyamide 1012 (PA1012) and poly(tetramethylene oxide) (PTMO). As a weakly segregated system, the PA1012-rich phase could break out the microdomains forged by the phase separation in the melt and big spherulites were observed after cooling. The PTMO segments and the film thickness were the key factors in determining the crystalline structure and morphology. As the content of PTMO component increased, an obvious morphological evolution was observed in the atomic force microscopy test. The morphological evolution was related to the increase of segregation strength and the dilution effect. The evolution of PA1012 crystalline structure along with the decreasing of film thickness resulted from the slow diffusion rate of crystallizable chains, the higher glass transition temperature, and the lower number of nuclei induced by the considerably thin film thickness.
引用
收藏
页数:9
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