Network models and their dynamics: Probes of topological structure

被引:3
|
作者
Blumen, A [1 ]
Jurjiu, A [1 ]
Koslowski, T [1 ]
机构
[1] Univ Freiburg, Inst Phys Chem, D-79104 Freiburg, Germany
关键词
fractals; mechanical relaxation; polymer networks; polymer dynamics; scaling;
D O I
10.1002/masy.200390004
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this work we focus on the mechanical relaxation of macromolecules. Based on linear response theory, this relaxation is in general related to the set of eigenmodes and eigenfunctions of the system. Of particular importance are situations which lead to scaling in the time and frequency domains. Thus the relaxation of star polymers, of dendrimers and of hyperbranched structures does not display scaling. On the other hand, one expects that the relaxation of fractals, as in fact that of linear chains, does scale. Here we numerically analyse the behavior of networks modelled through finite Sierpinski-type lattices, for which we have previously established that in the Rouse picture the mechanical relaxation scales in frequency and in time. As we show here, in the Zimm. model based on the preaveraged Oseen-tensor, the picture changes drastically; taking the hydrodynamic interactions into account leads to relaxation forms which do not scale.
引用
收藏
页码:141 / 150
页数:10
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