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The Role of Specific Interaction in Phase Behavior of Polyelectrolyte-Surfactant-Water Mixtures
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Pharmacy.ORCID iD: 0000-0002-0895-1180
2012 (English)In: Acta Chimica Slovenica, ISSN 1318-0207, Vol. 59, no 3, 503-512 p.Article in journal (Refereed) Published
Abstract [en]

Aqueous phase behavior and structures of phases were studied in systems containing sodium poly(styrenesulfonate), NaPSS, and complex salt CTAPSS, formed between cetyltrimethylammonium cations, CTA(+), and PSS- anions. It was shown that hydrophobic interaction of the polyion styrene groups with surfactant aggregates, which supports the strong electrostatic attraction between CTA(+) and PSS-, has a significant effect on phase behavior and structures. Only the disordered micellar (L-1) and the ordered hexagonal (H-1) phase were found that are connected over a broad two-phase region of L-1-H-1 coexistence. At water contents above 60 wt%, CTAPSS is easily dissolved in proportion to the amount of added NaPSS, whereas at lower water contents a large excess of NaPSS is needed to dissolve CTAPSS. Phase separation in the two-phase region is controlled by two tendencies: (i) to maximize the contact between the hydrophobic groups and micelles (assisted by hydrophobic interaction) and (ii) to form as dense phase as possible (assisted by both, electrostatic and hydrophobic interactions). Structural characteristics of soluble non-stoichiometric complexes from the L-1 phase show that hydrophobic interaction contributes also to a relatively small size of PSS-induced micelles and leads to a network-like association between PSS chains in which micelles serve as cross-links.

Place, publisher, year, edition, pages
2012. Vol. 59, no 3, 503-512 p.
Keyword [en]
Polyelectrolyte-surfactant complexes, phase behavior, electrostatic interactions, hydrophobic interactions, hexagonal structure, micellar phase
National Category
Chemical Sciences
URN: urn:nbn:se:uu:diva-183926ISI: 000308792600008OAI: oai:DiVA.org:uu-183926DiVA: diva2:565324
Available from: 2012-11-07 Created: 2012-11-05 Last updated: 2016-04-27Bibliographically approved

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