The James Franck Institute and the Department of Chemistry, The University of Chicago, Chicago, Illinois 60637, USA.
J Chem Phys. 2012 Feb 14;136(6):064903. doi: 10.1063/1.3681256.
The lattice cluster theory for solutions of telechelic polymer chains, developed in paper I, is applied to determine the enthalpy Δh(p) and entropy Δs(p) of self-assembly of linear telechelics and to evaluate the Flory-Huggins (FH) interaction parameter χ governing the phase behavior of these systems. Particular focus is placed on examining how these interaction variables depend on the composition of the solution, temperature, van der Waals and local "sticky" interaction energies, and the length of the individual telechelic chains. The FH interaction parameter χ is found to exhibit an entropy-enthalpy compensation effect between the "entropic" and "enthalpic" portions as either the composition or mass of the telechelic species is varied, providing unique theoretical insights into this commonly reported, yet, enigmatic phenomenon.
在论文 I 中发展的端基聚合物链溶液的格子簇理论被应用于确定线性端基聚合物自组装的焓变 Δh(p)和熵变 Δs(p),并评估控制这些体系相行为的弗洛里-哈金斯(FH)相互作用参数 χ。特别关注的是研究这些相互作用变量如何随溶液的组成、温度、范德华和局部“粘性”相互作用能以及单个端基链的长度而变化。发现 FH 相互作用参数 χ 表现出“熵”和“焓”部分之间的熵焓补偿效应,这是由于端基物种的组成或质量发生变化,为这一常见但神秘的现象提供了独特的理论见解。