Non-isothermal Crystallization Behavior of Poly(trimethylene terephthalate-co-isophthalate) Copolyesters

被引:1
作者
Shyr, Tien-Wei [1 ]
Tung, Chia-Hsin [1 ]
Liu, Yan-Ting [1 ]
机构
[1] Feng Chia Univ, Dept Fiber & Composite Mat, Taichung 40724, Taiwan
来源
ADVANCED ENGINEERING MATERIALS II, PTS 1-3 | 2012年 / 535-537卷
关键词
poly(trimethylene terephthalate-co-isophthalate); non-isothermal crystallization; POLY(ETHYLENE/TRIMETHYLENE TEREPHTHALATE) COPOLYESTERS; CRYSTAL-STRUCTURE; SEQUENCE DISTRIBUTION; MELTING BEHAVIOR; PHASE-CHANGE; KINETICS;
D O I
10.4028/www.scientific.net/AMR.535-537.1413
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Poly(trimethylene terephthalate-co-isophthalate) (TI) copolyesters were synthesized using different ratios of isophthalic acid (TA) and Terephthalic acid (TPA) with 1,3-propanediol (1,3-PDO). The compositions of TI copolyesters were analyzed using H-1 nuclear magnetic resonance (NMR). Non-isothermal melt- and cold-crystallization and subsequent melting behaviors were investigated using differential scanning calorimetry (DSC). For TIO, TI10, and TI20, non-isothermal crystallization kinetics were analyzed using a modified Avrami equation. The results show that the reaction rate of TPA with 1,3-PDO was similar with that of EPA with 1,3-PDO in TI copolyesters. Crystallization exothermic peak and melting endothermic peak were not observed in DSC traces with an increase of the relative amount of P-IP, to 41%. The Avrami exponent n is in the range of 3.5-4.2 for melt-crystallized TI copolyesters and between 3.0-3.2 for cold-crystallized copolyesters. It suggests that the crystallization from melt state corresponds to thermal nucleation but the crystallization from glassy state originates from predeterminated nuclei.
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页码:1413 / 1416
页数:4
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