Electrostatic self-assembly in polyelectrolyte-neutral block copolymers and oppositely charged surfactant solutions

被引:23
|
作者
Berret, JF
Oberdisse, J
机构
[1] CNRS, Unite Mixte Rech, Complex Fluids Lab, Cranbury, NJ 08512 USA
[2] CEA Saclay, Lab Leon Brillouin, F-91191 Gif Sur Yvette, France
关键词
polyelectrolyte; block copolymer; surfactant; complex colloids;
D O I
10.1016/j.physb.2004.04.027
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
We report on small-angle neutron scattering (SANS) of colloidal complexes resulting from the electrostatic self-assembly of polyelectrolyte-neutral copolymers and oppositely charged surfactants. The polymers are double hydrophilic block copolymers of low molecular weight (between 5000 and 50 000 g/mol). One block is a polyelectrolyte chain, which can be either positively or negatively charged, whereas the second block is neutral and in good solvent conditions. In aqueous solutions, surfactants with an opposite charge to that of the polyelectrolyte interact strongly with these copolymers. The two species associate into stable 100 nm-colloidal complexes which exhibit a core-shell microstructure. For different polymer/surfactant couples, we have shown that the core is constituted from densely packed surfactant micelles connected by the polyelectrolyte chains. The outer part of the complex is a corona formed by the neutral soluble chains. Using a model of aggregation based on a Monte-Carlo algorithm, we have simulated the internal structure of the aggregates. The model assumes spherical cages containing one to several hundreds of micelles in a closely packed state. The agreement between the model and the data is remarkable. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:204 / 206
页数:3
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