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Crystallization Kinetics and Spherulitic Morphologies of Biodegradable Poly(butylene succinate-co-diethylene glycol succinate) Copolymers
被引:16
|作者:
Liu, Guang-Chen
[1
]
Zeng, Jian-Bing
[1
]
Huang, Cai-Li
[1
]
Jiao, Ling
[1
]
Wang, Xiu-Li
[1
]
Wang, Yu-Zhong
[1
]
机构:
[1] Sichuan Univ, Natl Engn Lab Ecofriendly Polymer Mat Sichuan, Ctr Degradable & Flame Retardant Polymer Mat ERCP, Coll Chem,State Key Lab Polymer Mat Engn, Chengdu 610064, Peoples R China
基金:
中国国家自然科学基金;
关键词:
2 ALIPHATIC POLYESTERS;
ENZYMATIC DEGRADATION;
POLY(ETHYLENE SUCCINATE);
POLY(L-LACTIC ACID);
MISCIBILITY;
BEHAVIOR;
BLENDS;
COPOLYESTER;
TEMPERATURE;
POLYMERS;
D O I:
10.1021/ie303016v
中图分类号:
TQ [化学工业];
学科分类号:
0817 ;
摘要:
Poly(butylene succinate-co-diethylene glycol succinate) (P(BS-co-DEGS)) random copolymer was synthesized and characterized in a previous paper [Ind. Eng. Chem. Res. 2012, 51, 12258-12265]. In this paper, we focus on the isothermal crystallization behaviors of P(BS-co-DEGS). The isothermal crystallization kinetics, spherulitic morphology, and growth kinetics of P(BS-co-DEGS) were investigated by differential scanning calorimetry and polarized optical microscopy and compared with those of neat poly(butylene succinate) (PBS). The results suggest that the crystallization rate of P(BS-co-DEGS) was much slower than that of neat PBS and decreased with increase of DEGS content, while the crystallization mechanism remain unchanged. P(BS-co-DEGS) showed banded morphology, and the band spacing decreased with increase of DEGS content at a given supercooling. The spherulitic growth rate of P(BS-co-DEGS) decreased with increase in DEGS content. A transition from crystallization regime II to crystallization regime III occurred for all samples, and the transition shifted to lower temperatures with increase in DEGS content.
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页码:1591 / 1599
页数:9
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