疏水修饰缔合聚合物热可逆凝胶化过程中的分子内和分子间缔合

F. Tanaka, T. Koga
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引用次数: 28

摘要

在疏水改性水溶性缔合聚合物的热可逆凝胶化过程中,分子内缔合与分子间缔合相互竞争。前者导致分子内胶束,其疏水核心由亲水链环装饰。环的形成阻止了分子间的交联。本文从理论上详细阐述了小环对缔合聚合物溶液中具有多个交联结的溶胶/凝胶过渡的影响。在远旋缔合聚合物的情况下,这个问题在数学上等同于单功能和双功能聚合物的混合物。凝胶浓度随描述单环形成概率的参数而变化。六个基本链类别的相对居群推导为聚合物总浓度的函数,特别注意花胶束的形成。对于携带许多疏水分子的聚合物,通过使用模型链进行蒙特卡罗计算机模拟,观察分子内胶束化与分子间交联是如何竞争的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intramolecular and intermolecular association in thermoreversible gelation of hydrophobically modified associating polymers

In the thermoreversible gelation of hydrophobically modified water-soluble associating polymers, intramolecular association competes with intermolecular association. The former leads to intramolecular micelles with hydrophobic cores decorated by loops of hydrophilic chains. Loop formation prevents an intermolecular cross-linking. This paper theoretically details the effect of small loops on the sol/gel transition with multiple cross-link junctions in associating polymer solutions. In the case of telechelic associating polymers, the problem is shown to be mathematically equivalent to the mixture of monofunctional and bifunctional polymers. The gelation concentration changes with a parameter describing the probability of a single loop formation. Relative populations of the six fundamental chain categories are derived as a function of the total polymer concentration with special attention to the formation of flower micelles. For polymers carrying many hydrophobes, Monte Carlo computer simulation is carried out by using model chains to see how intramolecular micellization competes with intermolecular cross-linking.

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