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Effect of organic additives on formation and structure of polyelectrolyte‐oppositely charged surfactant complexes
Author(s) -
Zakharova J. A.,
Otdelnova M. V.,
Aliev I. I.,
Motyakin M. V.,
Wasserman A. M.,
Zezin A. B.,
Kabanov V. A.
Publication year - 2006
Publication title -
polymers for advanced technologies
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.61
H-Index - 90
eISSN - 1099-1581
pISSN - 1042-7147
DOI - 10.1002/pat.763
Subject(s) - polyelectrolyte , micelle , pulmonary surfactant , supramolecular chemistry , sodium dodecyl sulfate , spin probe , dynamic light scattering , spectroscopy , triton x 100 , electron paramagnetic resonance , butanol , chemistry , materials science , polymer chemistry , crystallography , polymer , molecule , organic chemistry , aqueous solution , nuclear magnetic resonance , nanoparticle , nanotechnology , biochemistry , physics , quantum mechanics , ethanol
Abstract Effect of butanol and Triton X‐100 on formation, supramolecular organization and local dynamics of poly( N ‐ethyl‐4‐vinylpyridinium)‐dodecyl sulfate complexes have been studied by UV spectroscopy, high‐speed sedimentation, laser light scattering and electron spin resonance (ESR) spectroscopy. It was found that solubilization of butanol promotes aggregation of the complex species in solution and results in contraction of the region in which water‐soluble complexes are formed. On the contrary, highly aggregated complexes disaggregate up to molecularly dispersed state upon addition of Triton X‐100. It was found that under the experimental conditions neither butanol (up to 3 wt%) nor Triton X‐100 ([Triton X‐100]/[sodium dodecylsulfate] ≤ 1:1) cause destruction of the complexes. The results of ESR spin probe and spin label studies show that in both cases supramolecular realignments are accompanied by a slight increase of the local molecular mobility of surfactant ions in the complex micelles, segmental mobility of polyelectrolyte being unchanged. Copyright © 2006 John Wiley & Sons, Ltd.