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Kinetics of phase separation and coarsening in dilute surfactant pentaethylene glycol monododecyl ether solutions
Author(s) -
Shinpei Tanaka,
Yoshihide Kubo,
Yasuhiro Yokoyama,
Akihiko Toda,
Kei Taguchi,
Hiroshi Kajioka
Publication year - 2011
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.3668349
Subject(s) - power law , phase inversion , phase (matter) , laminar flow , pulmonary surfactant , exponent , scaling , thermodynamics , micelle , chemistry , kinetics , materials science , chemical physics , mechanics , mathematics , physics , membrane , classical mechanics , geometry , organic chemistry , biochemistry , statistics , linguistics , philosophy , aqueous solution
We investigated the phase separation phenomena in dilute surfactant pentaethylene glycol monodedecyl ether (C(12)E(5)) solutions focusing on the growth law of separated domains. The solutions confined between two glass plates were found to exhibit the phase inversion, characteristic of the viscoelastic phase separation; the majority phase (water-rich phase) nucleated as droplets and the minority phase (micelle-rich phase) formed a network temporarily, then they collapsed into an usual sea-island pattern where minority phase formed islands. We found from the real-space microscopic imaging that the dynamic scaling hypothesis did not hold throughout the coarsening process. The power law growth of the domains with the exponent close to 1/3 was observed even though the coarsening was induced mainly by hydrodynamic flow, which was explained by Darcy's law of laminar flow.

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