Sequential reordering in condensation copolymers .1. Melting- and crystallization-induced sequential reordering in immiscible blends of poly(ethylene terephthalate) with polycarbonate or polyarylate

被引:39
|
作者
Fakirov, S
Sarkissova, M
Denchev, Z
机构
[1] TUBITAK ADV POLYMER MAT RES CTR, TR-80815 BEBEK, ISTANBUL, TURKEY
[2] UNIV SOFIA, STRUCT & PROPERTIES POLYMERS LAB, BU-1126 SOFIA, BULGARIA
关键词
D O I
10.1002/macp.1996.021970921
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Unlike previous attempts, the entire cycle of melting- and crystallization-induced reordering is realized in binary polymer blends in the following order: two homopolymers --> black copolymer --> random copolymer --> block copolymer. Blends of poly(ethylene terephthalate)(b)) (PET) acid bisphenol-A/polycarbonate (PC) as well as PET/polyarylate (PAr) blends, are annealed directly in a differential scanning calorimeter at 280 degrees C for various times. Scanning the samples in the heating mode reveals the complete disappearance of crystallization or melting in the blends where the ratio of PET/PC repeating units is less than 5.7/1.0. Such an amorphization is attributed to the formation of random copolymers. This statement is confirmed by NMR measurements, by the observation of one glass transition temperature T-g in the range between the initial two T(g)s, and by solubility tests. Once randomized, annealing the samples at 235 degrees C and 245 degrees C, i.e., below melting of PET, results in a T-g shift toward the T-g of PET as well as in reappearance of melting. This effect is accompanied by an eight-fold crystallinity increase in the equimolar blend, as compared to the randomized sample. The regenerated crystallization ability is explained by restoration of the blocks. According to previous findings, it is concluded that the considerable entropy increase is the main driving force of randomization. The rival trend to the formation of a block copolymer by sequential reordering is driven by the crystallization of PET blocks formed. The conclusion that the observed changes in the crystallization ability and T-g-values are based on sequential reordering is supported by experiments with samples containing increased amounts of transesterification catalyst leading to a much faster appearance of these changes. No randomization is observed with the blend composition ratio of repeating units PET/PC > 5.7/1.0. When the annealing is performed for 300 min at 165 degrees C, where no significant exchange reactions are expected to occur, no restoration of the crystallization ability is observed.
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页码:2837 / 2867
页数:31
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