Transition from miscibility to immiscibility in blends of poly(methyl methacrylate) and styrene-acrylonitrile copolymers with varying copolymer composition:: a DSC study

被引:28
作者
Cameron, N
Cowie, JMG
Ferguson, R
Ribelles, JLG
Estellés, JM
机构
[1] Univ Politecn Valencia, Ctr Biomat, E-46071 Valencia, Spain
[2] Univ Politecn Valencia, Dept Appl Thermodynam, E-46071 Valencia, Spain
[3] Heriot Watt Univ, Dept Chem, Edinburgh EH14 4AS, Midlothian, Scotland
关键词
polymer blends; glass transition; miscibility; structural relaxation; physical ageing; poly(methyl methacrylate); styrene-acrylonitrile copolymer;
D O I
10.1016/S0014-3057(01)00193-8
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 glass transition and the structural relaxation processes have been studied in blends of poly(methyl methacrylate) (PMMA) and styrene-acrylonitrile (SAN) copolymers with different acrylonitrile (AN) contents. The 50/50 wt.%) blend of PMMA with the SAN copolymer containing 30 wt.% of AN is immiscible, while blends with copolymers containing between 13 and 26 wt.%, of AN are miscible. Thus the upper limit of miscibility is between 26 and 30 wt.%(, of AN. The temperature dependence of the relaxation times of the conformational rearrangements of polymer chains around the glass transition have been determined in the blends and pure components by modelling DSC thermograms obtained after different thermal histories in each sample. The slope in the Arrhenius diagram log tau vs 1/T around the glass transition temperature is significantly smaller in the blend which is closer to the upper limit of miscibility than in the other miscible blends in which SAN copolymer contains less AN. The change of slope can be ascribed to a distribution in the glass transition temperatures of the different rearranging regions, reflecting the appearance of a microheterogeneity in the blend that cannot be detected as a double glass transition in the blend. (C) 2002 Published by Elsevier Science Ltd.
引用
收藏
页码:597 / 605
页数:9
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