화학공학소재연구정보센터
Journal of Colloid and Interface Science, Vol.585, 408-419, 2021
Multichain adsorption at fluid interfaces: Amphiphilic homopolymers vs copolymers
Hypothesis: At selective liquid-liquid interface, amphiphilic homopolymers, having groups with different affinity for the liquids in each monomer unit, would demonstrate higher occupation of the interfacial layer than copolymers with various distributions of groups and be advantageous as interface stabilizers. Experiments: By means of Langevin dynamics computer simulation, conformations of multiple chains of amphiphilic macromolecules adsorbed at the liquid-liquid interface were studied. Monomer units having different affinity for the liquids were distributed variously along the polymer chains. Homopolymers, amphiphilic at the level of an individual monomer unit, and copolymers with random, altermating and multiblock distribution of groups were considered. The surface coverage, structure of the layer, and spatial distribution of monomer units were investigated depending on the polymer concentration. Findings: Compared to copolymers with random, alternating and multiblock distributions of the groups, the interfacial layer concentration of amphiphilic homopolymer is about 1.5 times higher, the adsorbed layer is remarkably thinner, has membrane-like structure and is asymmetric with respect to interface boundary. Also, the adsorbed amphiphilic homopolymers form fewer loops and tails, most located on one side of the interface. This combination of properties is promising for practical application in modern self-assembling molecular devices. (C) 2020 Elsevier Inc. All rights reserved.