Isothermal crystallization of blends containing two thermotropic liquid crystalline polymers

被引:1
作者
Qian, Chen [1 ]
Wan, Guigui [2 ]
Frazier, Charles E. [2 ]
Baird, Donald G. [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Dept Chem Engn, Suite 245 Goodwin Hall,635 Prices Fork Rd, Blacksburg, VA 24061 USA
[2] Virginia Polytech Inst & State Univ, Dept Sustainable Biomat, Blacksburg, VA 24061 USA
基金
美国国家科学基金会;
关键词
Thermotropic liquid crystalline polymers; blends Isothermal crystallization; Rheology; SHEAR-INDUCED CRYSTALLIZATION; MECHANICAL-PROPERTIES; COPOLYESTERS; MISCIBILITY; POLYESTER; TRANSPORT; RHEOLOGY; BEHAVIOR; FLOW;
D O I
10.1016/j.mtcomm.2016.09.002
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The intention of this work is to determine how the isothermal crystallization behavior of a thermotropic liquid crystalline polymer (TLCP) can be adjusted by blending it with a pure TLCP of lower melting point. One TLCP (T-m similar to 350 degrees C) used is a copolyester synthesized from terephthalic acid, 4-hydroxybenzoic acid, hydroquinone and hydroquinone derivatives. The other TLCP (T-m similar to 280 degrees C) is a copolyesteramide of 60 mol% hydroxynaphthoic acid, 20 mol% terephthalic acid and 20 mol% 4-aminophenol. As the content of the low melting TLCP increases in the blends, the temperature at which isothermal crystallization occurs decreases. Comparing with pure TLCPs, the blend of 75% low melting TLCP crystallizes at a lower temperature than the pure matrix, and the blend remains as a stable super-cooled fluid in the temperature range from 220 to 280 degrees C for 1200 s. Because of the low energy released during the phase transition, small amplitude oscillatory shear (SAOS) is more sensitive to detecting the onset of isothermal crystallization than differential scanning calorimetry (DSC). (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:16 / 21
页数:6
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