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Surfactant self-assembly in oppositely charged polymer networks. Theory
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Pharmacy.
2009 (English)In: Journal of Physical Chemistry B, ISSN 1520-6106, E-ISSN 1520-5207, Vol. 113, no 39, 12903-12915 p.Article in journal (Refereed) Published
Abstract [en]

The interaction of ionic surfactants with polyion networks of opposite charge in an aqueous environment is analyzed theoretically by applying a recent theory of surfactant ion-polyion complex salts (J. Colloid. Int. Sci. 2009, 332, 183). The theory takes into account attractive and repulsive polyion-mediated interactions between the micelles, the deformation of the polymer network, the mixing of micelles, polyion chains, and simple ions with water, and the hydrophobic free energy at the micelle surface. The theory is used to calculate binding isotherms, swelling isotherms, surfactant aggregation numbers, compositions of complexes,and phase structure under various conditions. Factors controlling the gel volume transition and conditions for core/shell phase coexistence are investigated in detail, as well as the influence of salt. In particular, the interplay between electrostatic and elastic interactions is highlighted. Results from theory are compared with experimental data reported in the literature. The agreement is found to be semiquantitative or qualitative. The theory explains both the discrete volume transition observed in systems where the surfactant is in excess over the polyion and the core/shell phase coexistence in systems where the polyion is in excess.

Place, publisher, year, edition, pages
2009. Vol. 113, no 39, 12903-12915 p.
National Category
Pharmaceutical Sciences
URN: urn:nbn:se:uu:diva-109459DOI: 10.1021/jp904866tISI: 000269999400009PubMedID: 19728696OAI: oai:DiVA.org:uu-109459DiVA: diva2:272501
Available from: 2009-10-15 Created: 2009-10-15 Last updated: 2010-07-06Bibliographically approved

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