Microphase separation in cross-linked polymer blends

被引:5
|
作者
Klopper, A. V. [1 ]
Svaneborg, Carsten [2 ]
Everaers, Ralf [3 ]
机构
[1] Max Planck Inst Phys Komplexer Syst, D-01187 Dresden, Germany
[2] Univ Aarhus, Dept Chem & Interdisciplinary Nanosci Ctr iNano, DK-8000 Aarhus, Denmark
[3] Univ Lyon, Phys Lab, Ecole Normale Super Lyon, CNRS,UMR 5672, F-69364 Lyon 07, France
来源
EUROPEAN PHYSICAL JOURNAL E | 2009年 / 28卷 / 01期
关键词
MOLECULAR-DYNAMICS SIMULATION; SPIN-GLASSES; MELTS; SCATTERING; NETWORKS; BEHAVIOR; LIQUIDS; STRAIN; CHAIN; SANS;
D O I
10.1140/epje/i2008-10420-6
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 investigate the behaviour of randomly cross-linked (co)polymer blends using a combination of replica theory and large-scale molecular dynamics simulations. In particular, we derive the analogue of the random phase approximation for systems with quenched disorder and show how the required correlation functions can be calculated efficiently. By post-processing simulation data for homopolymer networks we are able to describe neutron scattering measurements in heterogeneous systems without resorting to microscopic detail and otherwise unphysical assumptions. We obtain structure function data which illustrate the expected microphase separation and contain system-specific information relating to the intrinsic length scales of our networks.
引用
收藏
页码:89 / 96
页数:8
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