Out of equilibrium dynamics of poly(vinyl methyl ether) segments in miscible poly(styrene)-poly(vinyl methyl ether) blends -: art. no. 031805
被引:83
作者:
Lorthioir, C
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机构:Univ Basque Country, Dept Fis Mat, San Sebastian 20080, Spain
Lorthioir, C
Alegría, A
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h-index: 0
机构:Univ Basque Country, Dept Fis Mat, San Sebastian 20080, Spain
Alegría, A
Colmenero, J
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h-index: 0
机构:Univ Basque Country, Dept Fis Mat, San Sebastian 20080, Spain
Colmenero, J
机构:
[1] Univ Basque Country, Dept Fis Mat, San Sebastian 20080, Spain
[2] Univ Basque Country, Fac Quim, Unidad Fis Mat Ctr Mixto CSIC UPV EHU, San Sebastian 20080, Spain
[3] Donostia Int Phys Ctr, San Sebastian 20018, Spain
来源:
PHYSICAL REVIEW E
|
2003年
/
68卷
/
03期
关键词:
D O I:
10.1103/PhysRevE.68.031805
中图分类号:
O35 [流体力学];
O53 [等离子体物理学];
学科分类号:
070204 ;
080103 ;
080704 ;
摘要:
The local dynamics of the low-T-g component in a polymer blend, dynamically asymmetric poly(styrene)-poly(vinyl methyl ether) (PS-PVME), is studied below the glass transition, via dielectric relaxation spectroscopy. A particular attention has been paid to blends with a high PS content (PS weight fraction higher than 50%). A relaxation process, slower than the localized motions inducing the PVME secondary relaxations, is detected. Even though these blends fall out of equilibrium in this temperature regime, the structural recovery process is not efficient on the time scale of this PVME motional process. This relaxation is attributed to rather localized, weakly cooperative PVME motions resulting from the topological constraints imposed by the frozen PS chains.