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与表面接触的多嵌段共聚物溶液:自组装、吸附和渗滤

Multiblock copolymer solutions in contact with a surface: self-assembly, adsorption, and percolation.

作者信息

Hugouvieux Virginie, Kolb Max

机构信息

INRA, UMR1083 SPO , F-34060 Montpellier, France.

出版信息

Langmuir. 2014 Oct 21;30(41):12400-10. doi: 10.1021/la502945k. Epub 2014 Oct 6.

Abstract

Amphiphilic copolymers are often used as compatibilizing or stabilizing agents, either in solution or at surfaces. In the special case of multiblock copolymers the connectivity of the blocks combines with the antagonistic behavior of the different types of blocks. Here we report on the behavior of solutions of amphiphilic multiblock copolymers with a large number of blocks and a low fraction of solvophobic monomers in contact with an attractive surface. Using lattice Monte Carlo simulations, the influence on the structures of the solvent quality and the type of surface from noninteracting to strongly attractive to the solvophobic monomers can be assessed. In the presence of a surface bulk micelles are formed that are not different in size and shape from the micelles observed in the absence of a surface. When increasing the surface attraction, solvophobic monomers tend to adsorb either as isolated blocks or forming surface micelles. Evidence is given of a surface concentration threshold above which surface micelles can form due to microphase separation. These surface micelles are in equilibrium with bulk micelles, some of which are connected to the surface through a path of either hydrophobic and/or hydrophilic blocks or hydrophobic cross-links, or both. The size distributions of bulk and connected micelles are similar. With increasing surface concentration surface micelles get organized due to the steric repulsion between core-shell surface micelles. Moreover, these organized surface micelles percolate. The connected micelles form a concentrated layer parallel to the attractive surface. In addition, these systems are governed by two very different time scales: The fast one leads to micellar self-assembly in the bulk and at the surface while the slow one prevents the system from reaching equilibrium in the course of the simulations and corresponds to the transfer of copolymers from the bulk to the attractive surface.

摘要

两亲性共聚物通常用作增容剂或稳定剂,无论是在溶液中还是在表面。在多嵌段共聚物的特殊情况下,嵌段的连接性与不同类型嵌段的拮抗行为相结合。在此,我们报告了具有大量嵌段且疏溶剂单体比例较低的两亲性多嵌段共聚物溶液与有吸引力的表面接触时的行为。通过晶格蒙特卡罗模拟,可以评估溶剂质量和表面类型(从与疏溶剂单体无相互作用到强吸引)对结构的影响。在有表面存在的情况下,会形成本体胶束,其大小和形状与无表面时观察到的胶束并无不同。当增加表面吸引力时,疏溶剂单体倾向于以孤立嵌段的形式吸附或形成表面胶束。有证据表明存在一个表面浓度阈值,高于该阈值时由于微相分离可形成表面胶束。这些表面胶束与本体胶束处于平衡状态,其中一些通过疏水和/或亲水嵌段路径或疏水交联或两者相连与表面相连。本体胶束和相连胶束的尺寸分布相似。随着表面浓度的增加,表面胶束由于核壳表面胶束之间的空间排斥而有序排列。此外,这些有序的表面胶束会发生渗滤。相连的胶束形成平行于有吸引力表面的浓缩层。此外,这些体系受两个非常不同的时间尺度支配:快的时间尺度导致本体和表面胶束的自组装,而慢的时间尺度则阻止体系在模拟过程中达到平衡,并且对应于共聚物从本体向有吸引力表面的转移。

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