Random packing of model polymers: local structure, topological hindrance and universal scaling

被引:47
|
作者
Laso, Manuel [1 ]
Karayiannis, Nikos Ch. [1 ]
Foteinopoulou, Katerina [1 ]
Mansfield, Marc L. [2 ]
Kroeger, Martin [3 ]
机构
[1] Univ Politecn Madrid, Inst Optoelect & Microsyst ISOM, E-28006 Madrid, Spain
[2] Stevens Inst Technol, Dept Chem & Chem Biol, Hoboken, NJ 07079 USA
[3] Swiss Fed Inst Technol, Dept Mat, CH-8093 Zurich, Switzerland
关键词
RANDOM CLOSE PACKING; PRIMITIVE PATH IDENTIFICATION; MONTE-CARLO; ENTANGLEMENT STATISTICS; HARD-SPHERES; MELTS; SIMULATIONS; DYNAMICS; POLYETHYLENE; TEMPERATURE;
D O I
10.1039/b820264h
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
The random packing of rigid objects has not only engrossed mathematicians since biblical times but is receiving attention for numerous applications and processes involving microgels, granular media, colloids, glasses, liquids, synthetic polymers and biomolecules. While dense random assemblies of single hard spheres have been extensively investigated both experimentally and theoretically over the past 50 years, it was only recently that analogous problems for chains of hard spheres have been addressed. We highlight the relevance of these recent advances, and describe the most salient characteristics of the "maximally random jammed'' state for hard sphere chains. Particular emphasis is placed on the scaling behavior of chain dimensions and topology with packing density. We also discuss the potentially far-reaching implications of an unexpected connection that has been found between entanglements (intermolecular constraints) and knots (of intramolecular origin) regarding their dependence on volume fraction.
引用
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页码:1762 / 1770
页数:9
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