Structure formation and miscibility of sheets from PBT and LCP blends

被引:0
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作者
K. Qi
K. Nakayama
机构
[1] National Institute of Advanced Industrial Science and Technology,Macromolecular Technology Research Center
来源
关键词
Differential Scanning Calorimetry; Glass Transition Temperature; Transesterification; Terephthalate; Dynamic Mechanical Analysis;
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摘要
Sheets from blends containing poly(butylene terephthalate) (PBT) and liquid crystalline polymer (LCP) were prepared using a twin-screw extruder. The LCP used is a copolymer composed of 20 mol % ethylene terephalate (PET) and 80 mol % p-hydroxybenzoic acid (PHB). Thermal behavior, viscoelastic properties, and structure of the sheets of various compositions were investigated by using differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), microwave orientation analysis (MOA), and wide angle x-ray diffraction (WAXD). X-ray diffractograms of extruded sheets from PBT, LCP, and their blends show a high degree of orientation along extrusion direction. The orientation is mainly due to the high crystallization rate of PBT, although crystallization and orientation of PBT in the PBT and LCP blends could also be induced by adding LCP. In the PBT and LCP blends, the thermal properties of the constituents are slightly changed indicating that PBT and LCP are partially miscible. DSC measurements show that as the amount of LCP added to the blend increased, the melting point Tm of PBT in the blends decreased. The single glass transition temperature Tg for the PBT and LCP was observed by DMA. Furthermore, no evidence of transesterification in PBT and LCP blends was observed by WAXD.
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页码:3207 / 3213
页数:6
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