Enhanced crystallization behaviors of poly(ethylene terephthalate) via adding expanded graphite and poly(ethylene glycol)

被引:8
|
作者
Su, Juan-juan [1 ]
Yang, Guang-hui [1 ]
Zhou, Tian-nan [1 ]
Gao, Xiang [1 ]
Wang, Ke [1 ]
Fu, Qiang [1 ]
机构
[1] Sichuan Univ, Coll Polymer Sci & Engn, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金;
关键词
Poly(ethylene terephthalate); Expanded graphite; Poly(ethylene glycol); Crystallization; Nucleation; POLYETHYLENE TEREPHTHALATE; NUCLEATION; NANOCOMPOSITES; KINETICS; SALTS; STATE;
D O I
10.1007/s00396-012-2809-5
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A compound additive system consisting of expanded graphite (EG) and poly(ethylene glycol) (PEG) was designed to enhance the crystallization of poly(ethylene terephthalate) (PET). In this additive system, EG acted as a heterogeneous nucleating agent to reduce energy barrier for nucleation, while PEG played as plasticizer to improve mobility of PET chains. Simultaneously adding EG and PEG resulted in faster crystallization kinetics than the cases of solely adding EG or PEG in both of non-isothermal and isothermal crystallization processes, indicating a synergistic effect of EG and PEG on enhancing PET crystallization. However, for non-isothermal crystallization process, in which crystallization occurred from a cooling melt, EG played a dominant role. As to isothermal crystallization process where crystallization took place in a super-cooling state, PEG seemed to be more important. Moreover, the chain conformation change among the semi-crystalline PET specimens was ascertained by Fourier transform infrared spectroscopy.
引用
收藏
页码:911 / 917
页数:7
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