On the crystallization behavior of a poly(stearyl methacrylate) comb-like polymer inside a nanoscale environment

被引:12
|
作者
Li, Shuqin [1 ]
Wang, Haixia [1 ]
Liu, Luntao [1 ]
Xu, Hongxing [1 ]
Shi, Haifeng [1 ]
机构
[1] Tianjin Polytech Univ, Tianjin Key Lab Adv Fibers & Energy Storage, Sch Mat Sci & Engn, Tianjin 300387, Peoples R China
来源
CRYSTENGCOMM | 2018年 / 20卷 / 45期
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
CONFINED CRYSTALLIZATION; POLY(ETHYLENE OXIDE); BLEND FIBERS; PHASE-CHANGE; KINETICS; POLYSTYRENE; PERFORMANCE; TRANSITION; ETHER;
D O I
10.1039/c8ce01378k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Using a composite hard and soft template, approached by a macroscopic polystyrene (PS) matrix and a microscopic coaxial nanofiber, the crystallization of poly(stearyl methacrylate) (PSMA), a comb-like polymer under nanoscale conditions was explored. Crystalline structures and morphologies of a polyethylene terephthalate (PET)/PSMA nanofiber (NF) and PET/PSMA@PS composite membrane (CM) were characterized by differential scanning calorimetry, scanning electron microscopy, and transmission electron microscopy. Regulated by an orientated PET NF shell and PS matrix, the PSMA inner core showed a nanosize-dependent crystallization phenomenon. A hard or soft condition was approached by controlling the annealing temperature below 60 degrees C or above 120 degrees C, respectively. Confined crystallization in the entrapped PSMA was demonstrated, and PET/PSMA@PS CM showed a longer half-time of crystallization (t(1/2) = 1.69) than that of PET/PSMA NF (t(1/2) = 1.14). Therefore, against bulk PSMA (t(1/2) = 0.61), the increased crystallization time under nanoscale conditions was attributed to the reduced chain relaxation and mobility of alkyl groups.
引用
收藏
页码:7348 / 7356
页数:9
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