Theoretical Chemistry, Chemical Centre, Lund University, Lund, Sweden.
Langmuir. 2012 Mar 6;28(9):4223-32. doi: 10.1021/la204576q. Epub 2012 Feb 27.
We use a recently developed continuum theory to expand on an exact treatment of the interfacial properties of telechelic polymers displaying Schulz-Flory polydispersity. Our results are remarkably compact and can be derived from the properties of equilibrium, ideal polymers at interfaces. A new surface adsorption transition is identified for ideal telechelic chains, wherein the central block is an equilibrium polymer. This transition occurs in the limit of strong end adsorption. Additionally, closed expressions are derived for the ideal continuum telechelic chain in contact with two large spheres, using the Derjaguin approximation. We analyze the interactions between colloids as a function of polydispersity and molecular weight, and the results are compared with polymer density functional theory in the dilute limit. Significant variations in polymer mediated forces are observed as a function of polydispersity, molecuar weight, and chain stiffness.
我们使用最近发展的连续体理论,对具有 Schulz-Flory 多分散性的端基聚合物的界面特性进行了精确处理。我们的结果非常简洁,可以从界面处平衡、理想聚合物的特性中推导出来。对于理想的端基聚合物链,我们确定了一种新的表面吸附转变,其中中央嵌段是平衡聚合物。这种转变发生在强端吸附的极限下。此外,我们还使用 Derjaguin 近似法,推导出了与两个大球体接触的理想连续体端基聚合物链的封闭表达式。我们分析了胶体之间的相互作用,作为多分散性和分子量的函数,结果与稀溶液中聚合物密度泛函理论进行了比较。观察到聚合物介导的力随着多分散性、分子量和链刚性的变化而发生显著变化。