ON THE CONSTRUCTION OF COARSE-GRAINED MODELS FOR LINEAR FLEXIBLE POLYMER-CHAINS - DISTRIBUTION-FUNCTIONS FOR GROUPS OF CONSECUTIVE MONOMERS

被引:107
|
作者
BASCHNAGEL, J
BINDER, K
PAUL, W
LASO, M
SUTER, UW
BATOULIS, I
JILGE, W
BURGER, T
机构
[1] BAYER AG,ZENT FORSCH & ENTWICKLUNG,W-5090 LEVERKUSEN,GERMANY
[2] SWISS FED INST TECHNOL,INST POLYMERE,CH-8092 ZURICH,SWITZERLAND
来源
JOURNAL OF CHEMICAL PHYSICS | 1991年 / 95卷 / 08期
关键词
D O I
10.1063/1.461826
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
Coarse-grained models for linear flexible polymers are constructed defining effective segments by taking together n successive chemical monomers of a polymer chain, for n = 1,2,3,.. . The distribution function P(n)(l) for the length l of such effective segments is studied as well as the distribution function P(n)(V) of the angle between successive effective segments. If n is large enough, all these distribution functions tend towards universal limiting functions. For small n, information on chemical structure and effective potentials for the various degrees of freedom of the polymer chains is still preserved. Using polyethylene (PE) as one example, it is shown that these distribution functions for small n depend somewhat on the choice of the model for the effective potential (and the degrees of freedom included). Bisphenol-A-polycarbonate (BPA-PC) as a second example, serves to study to which extent these distribution functions P(n)(l) and P(n)(V) differ for chemically different polymers, such as PE and BPA-PC. Consequences for the molecular modeling of polymeric materials are briefly discussed.
引用
收藏
页码:6014 / 6025
页数:12
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