Is there a higher-order mode coupling transition in polymer blends?

被引:42
|
作者
Moreno, Angel J.
Colmenero, Juan
机构
[1] Donostia Int Phys Ctr, San Sebastian 20018, Spain
[2] Univ Basque Country, EHU, Dept Fis Mat, San Sebastian 20080, Spain
[3] UPV, CSIC, Ctr Mixto, Unidad Fis Mat, San Sebastian 20080, Spain
来源
JOURNAL OF CHEMICAL PHYSICS | 2006年 / 124卷 / 18期
关键词
D O I
10.1063/1.2198202
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present simulations on a binary blend of bead-spring polymer chains. The introduction of monomer size disparity yields very different relaxation times for each component of the blend. Competition between two different arrest mechanisms, namely, bulklike dynamics and confinement, leads to an anomalous relaxation scenario for the fast component, characterized by sublinear time dependence for mean squared displacements, or logarithmic decay and convex-to-concave crossover for density-density correlators. These anomalous dynamic features, which are observed over time intervals extending up to 4 decades, strongly resemble predictions of mode coupling theory for nearby higher-order transitions. Chain connectivity extends anomalous relaxation over a wide range of blend compositions. (c) 2006 American Institute of Physics.
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页数:6
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