Microstructure and crystallization of melt-mixed poly(ethylene terephthalate)/poly(ethylene isophthalate) blends

被引:10
作者
Kint, DPR
de Ilarduya, AM
Sansalvadó, A
Ferrer, J
Muñoz-Guerra, S
机构
[1] Univ Politecn Catalunya, ETSEIB, Dept Engn Quim, Barcelona 08028, Spain
[2] Catalana Polimers SL, Barcelona 08820, Spain
关键词
poly(ethylene terephthalate) (PET); poly(ethylene isophthalate) (PEI); blends; block copolymers; microstructure;
D O I
10.1002/app.13048
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Physical blends of poly(ethylene terephthalate) (PET) and poly(ethylene isophthalate) (PEI), abbreviated PET/PEI (80/20) blends, and of PET and a random poly(ethylene terephthalate-co-isophthalate) copolymer containing 40% ethylene isophthalate (PET60I40), abbreviated PET/PET60I40 (50/50) blends, were melt-mixed at 270degreesC for different reactive blending times to give a series of copolymers containing 20 mol % of ethylene isophthalic units with different degrees of randomness. C-13-NMR spectroscopy precisely determined the microstructure of the blends. The thermal and mechanical properties of the blends were evaluated by DSC and tensile assays, and the obtained results were compared with those obtained for PET and a statistically random PETI copolymer with the same composition. The microstructure of the blends gradually changed from a physical blend into a. block copolymer, and finally into a random copolymer with the advance of transreaction time. The melting temperature and enthalpy of the blends decreased with the progress of melt-mixing. Isothermal crystallization studies carried out on molten samples revealed the same trend for the crystallization rate. The effect of reaction time on crystallizability was more pronounced in the case of the PET/PET60I40 (50/50) blends. The Young's modulus of the melt-mixed blends was comparable to that of PET, whereas the maximum tensile stress decreased with respect to that of PET. All blend samples showed a noticeable brittleness. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:3076 / 3086
页数:11
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