The mechanism of thickness selection in the Sadler-Gilmer model of polymer crystallization

被引:27
|
作者
Doye, JPK
Frenkel, D
机构
[1] Univ Cambridge, Chem Lab, Cambridge CB2 1EW, England
[2] FOM, Inst Atom & Mol Phys, NL-1098 SJ Amsterdam, Netherlands
来源
JOURNAL OF CHEMICAL PHYSICS | 1999年 / 110卷 / 14期
关键词
D O I
10.1063/1.478613
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
Recent work on the mechanism of polymer crystallization has led to a proposal for the mechanism of thickness selection which differs from those proposed by the surface nucleation theory of Lauritzen and Hoffman and the entropic barrier model of Sadler and Gilmer. This has motivated us to reexamine the model used by Sadler and Gilmer. We again find a fixed-point attractor which describes the dynamical convergence of the crystal thickness to a value just larger than the minimum stable thickness, l(min). This convergence arises from the combined effect of two constraints on the length of stems in a layer: it is unfavorable for a stem to be shorter than l(min) and for a stem to overhang the edge of the previous layer. The relationship between this new mechanism and the explanation given by Sadler and Gilmer in terms of an entropic barrier is discussed. We also examine the behavior of the Sadler-Gilmer model when an energetic contribution from chain folds is included. (C) 1999 American Institute of Physics.
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页码:7073 / 7086
页数:14
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