Ordering and structure formation in triblock copolymer solutions .2. Small angle X-ray scattering and calorimetric observations

被引:26
作者
Soenen, H
Liskova, A
Reynders, K
Berghmans, H
Winter, HH
Overbergh, N
机构
[1] KATHOLIEKE UNIV LEUVEN,DEPT CHEM,B-3001 HEVERLEE,BELGIUM
[2] UNIV MASSACHUSETTS,DEPT CHEM ENGN,AMHERST,MA 01003
[3] UNIV MASSACHUSETTS,DEPT POLYMER SCI & ENGN,AMHERST,MA 01003
[4] RAYCHEM NV,RES & DEV,B-3010 KESSEL,BELGIUM
关键词
block copolymer; disordering temperature; micro phase separation;
D O I
10.1016/S0032-3861(97)00107-9
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 morphology and thermal properties of a poly(styrene)-poly(ethylene, butylene) triblock copolymer in the presence of a selective solvent has been investigated, using small-angle X-ray scattering (SAXS) and calorimetry (d.s.c.). The temperature dependence of the SAXS profiles indicated a transition, which was associated with a thermal destruction of the superlattice, preserving the nearest neighbour distance between the micro domains. The transition temperature was referred to as the disordering temperature (T-d). On heating, the loss of long range order was observed as a sudden broadening of the line profiles of the first order peak. At higher temperatures a gradual disappearance of this first order peak was interpreted as a gradual dissolution of the micro domain structure. Simultaneously, calorimetric investigations revealed two transitions on heating: at lower temperatures a glass transition, followed by an endothermic transition. The onset of the endotherm corresponded to T-d. In addition, the onset of how, which has been reported in Part I of this series, also corresponded to T-d Annealing at intermediate temperatures resulted in the formation of large scale ordering. This ordering could be followed by X-ray scattering and corresponded to changes observed in the rheological behaviour. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:5661 / 5665
页数:5
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