Crystallization kinetics and the fine morphological evolution of poly(ethylene oxide)/ionic liquid mixtures

被引:10
作者
Li, Wen-ze [1 ]
Niu, Yan-hua [1 ]
Zhou, Chen-ting [1 ]
Luo, Huan [1 ]
Li, Guang-xian [1 ]
机构
[1] Sichuan Univ, Coll Polymer Sci & Engn, State Key Lab Polymer Mat Engn China, Chengdu 610065, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
PEO; BMIM][PF6; Crystallization kinetics; Spherulite morphologies; SOLID POLYMER ELECTROLYTES; BETA-NUCLEATING AGENT; X-RAY-SCATTERING; IONIC LIQUID; SPHERULITIC CRYSTALLIZATION; ISOTACTIC POLYPROPYLENE; PHASE-SEPARATION; BLOCK-COPOLYMERS; ROOM-TEMPERATURE; METAL-IONS;
D O I
10.1007/s10118-017-1997-3
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The overall crystallization kinetics and spherulite morphologies of miscible poly(ethylene oxide) (PEO)/1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF6]) mixtures were studied by differential scanning calorimetry (DSC), polarized optical microscopy (POM) and rheological measurements. The finer crystal structures were further detected by wide angle X-ray diffraction (WAXD) and small angle X-ray scattering (SAXS). Crystallization of PEO is largely suppressed by [BMIM][PF6] addition especially at higher ionic liquid (IL) concentrations above 20 wt%. Both the overall crystallization rate and the spherulite growth decrease with the increase of IL content and crystallization temperature; however, the crystallization mechanism keeps unchanged as evidenced by the similar Avrami exponent n and WAXD results. The addition of [BMIM][PF6] could induce more nuclei to some extent, but the induction time of crystallization is evidently prolonged, and a linear to non-linear transition of the spherulite growth (R ae t to R ae t (1/2)) can be observed. At higher IL concentration, the spherulite texture changes apparently from particular serrated to branch surface due to the diffusion-controlled growth and the dilution effect, which also as a main factor contributes to the increasing trend of the long period of crystals.
引用
收藏
页码:1402 / 1414
页数:13
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