Reverse micelles with spines: L2 phases of surfactant ion - Polyion complex salts, n-alcohols and water investigated by rheology, NMR diffusion and SAXS measurements

Juliana Silva Bernardes, Marcelo Alves Da Silva, Lennart Piculell, Watson Loh

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Homogeneous alcoholic isotropic solutions (L2 phases) of "complex salts" of hexadecyltrimethylammonium neutralized by polyacrylate CTAPAn (n = 30 or 6000), in the presence of water were examined at 25 °C by means of small-angle X-ray scattering (SAXS), rheology and NMR self-diffusion measurements for different n-alcohols (octanol, hexanol and butanol) and at varying water contents. The greater water solubility and the slower water self-diffusion coefficients in these L2 phases, when compared to results with surfactant-free alcohols, suggested that these phases are composed of reverse aggregates with water in their cores. A comparatively rapid self-diffusion of the surfactant ion in butanol suggested a significant fraction of "free" surfactant ions, dissociated from the reverse aggregates. Rheological data confirmed that the obtained viscoelastic properties were consistent with a system containing entangled elongated micelles, whose properties were controlled by the polyion chain length. NMR diffusion measurements for complex salt solutions with the shorter counter-polyion (CTAPA30) produced estimates of the aggregate lengths that were close to the extended length of one PA30 chain. In summary, these results support the formation of aggregates composed by surfactant decorated polyion chains with a water core, whose properties are determined by the polyion chain length, behaving like reverse micelles with spines.

Original languageEnglish
Pages (from-to)144-153
Number of pages10
JournalSoft Matter
Volume6
Issue number1
DOIs
Publication statusPublished - 11 Nov 2009

ASJC Scopus subject areas

  • Chemistry(all)
  • Condensed Matter Physics

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