Confinement effects on water structure in membrane lyotropic phases

被引:28
|
作者
Guegan, Regis [1 ]
机构
[1] Univ Orleans, CNRS, Inst Sci Terre Orleans, F-45071 Orleans 2, France
关键词
Non-ionic surfactant; Lamellar; Sponge phase; Water structure; Raman scattering; OH STRETCHING REGION; LIQUID-CRYSTAL; VIBRATIONAL-SPECTRUM; RAMAN-SPECTRUM; SPONGE PHASES; DYNAMICS; SURFACTANT; ICE; SIMULATION; LAMELLAR;
D O I
10.1016/j.jcis.2011.02.035
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The change of the water structure in aqueous solutions of the tri-ethyleneglycol mono n-decyl ether (C10E3) was studied by micro Raman scattering. The results obtained on the O-H stretching band show that the behavior of the hydrogen bonding (H-bonds) water network can be used as a probe to follow the lamellar (L-alpha) to sponge (L-3) phase transition. In the lamellar phase, the stack of the surfactant molecules aggregated into a two-dimensional structure (membrane) acts as a soft confinement system for the H-bond water network of which the regular tetrahedral structure is perturbed. The change of the planar organization of the membranes to a highly disordered and infinite array of bilayers in the sponge phase amplifies the surface of contact between amphiphilic surfactant and water molecules which drives a strong disruption of the regular tetrahedral H-bonding water network. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:485 / 490
页数:6
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