Characterization, Crystallization Kinetics, and Melting Behavior of Poly(ethylene succinate) Copolyester Containing 7 mol % Butylene Succinate

被引:12
|
作者
Lu, Hsin-Ying [1 ]
Lu, Shih-Fu [1 ]
Chen, Ming [1 ]
Chen, Chi He [1 ]
Tsai, Chia-Jung [1 ]
机构
[1] Natl Sun Yat Sen Univ, Inst Mat Sci & Engn, Kaohsiung 80424, Taiwan
关键词
crystallization; morphology; polyesters; TEMPERATURE MODULATED DSC; RIGID AMORPHOUS FRACTION; CO-ETHYLENE SUCCINATE)S; POLY(BUTYLENE SUCCINATE); ENZYMATIC DEGRADATION; POLY(TETRAMETHYLENE SUCCINATE); PHYSICAL-PROPERTIES; ETHER KETONE); POLYESTERS; GLYCOL;
D O I
10.1002/app.29975
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 copolyester was synthesized and characterized as having 92.7 mol % ethylene succinate units and 7.3 mol % butylene succinate (BS) units in a random sequence, as determined by the use of nuclear magnetic resonance. Isothermal crystallization kinetics of this copolyester was examined in the temperature range (T-c) from 30 to 80 degrees C with the use of differential scanning calorimetry (DSC). The melting behavior after isothermal crystallization was studied with DSC by varying the T-c the heating rate, and the crystallization time. The complex melting behavior involves both mechanisms of various lamellar crystals and melting-recrystallization-remelting. As the T-c increases, the contribution of recrystallization gradually decreases and finally disappears. The Hoffman-Weeks linear plot yielded an equilibrium melting temperature of 111.1 degrees C, which is 1.6 degrees C less than that of poly(ethylene succinate) (PES). The kinetic analysis of the spherulitic growth rates (G) indicated that a regime II -> III transition occurred at similar to 59 degrees C (T-II -> III), which is similar to 11 degrees C less than that of PES. The overall crystallization rate, T-II -> III and G indicate that the random incorporation of only 7.3 mol % BS units into PES significantly inhibits the crystallization rate of PES. Finally, the morphology of melt-crystallized samples was examined using polarized light microscopy and scanning electron microscopy. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 113: 876-886, 2009
引用
收藏
页码:876 / 886
页数:11
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