In-plane distribution in mixtures of cationic and anionic surfactants

被引:35
作者
Carriere, David [1 ]
Belloni, Luc [1 ]
Deme, Bruno [2 ]
Dubois, Monique [1 ]
Vautrin, Claire [1 ]
Meister, Annette [3 ]
Zemb, Thomas [1 ,4 ]
机构
[1] CEA, IRAMIS, SIS2M, LIONS, F-91191 Gif Sur Yvette, France
[2] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
[3] Univ Halle Wittenberg, Inst Phys Chem, D-06108 Halle, Germany
[4] ENSCM, CNRS, UMR 5257, CEA,ICSM,UM2, F-30207 Bagnols Sur Ceze, France
关键词
ANGLE NEUTRON-SCATTERING; FREE CATANIONIC SURFACTANT; SPONTANEOUS VESICLES; PHASE-BEHAVIOR; MICELLES; SYSTEMS; WATER; SANS; POLYMORPHISM; SEGREGATION;
D O I
10.1039/b912286a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Mixtures of cationic and anionic surfactants, also called "catanionic'' mixtures, self-assemble into aggregates which show a rich variety of morphologies in the nanometre to micron range controlled by the molar ratio between surfactants. At the molecular scale, little is known about the local distribution of surfactants in the bilayer. Here, we determine the in-plane distribution of the cationic and anionic surfactants in catanionic bilayers using neutron scattering and the contrast matching technique. The coexistence of two different in-plane orders is experimentally demonstrated: both surfactants share a common two-dimensional hexagonal lattice with a long-range order, but the distribution of alternate (+) and (-) charged head groups shows only a two-dimensional liquid-like local order. Comparing experiments and Monte-Carlo simulations, we establish that this lateral liquid order is attenuated by the counterions of the bilayers, but is less than expected in a mean-field approach. This demonstrates that electrostatic interactions participate in, but do not completely determine, the local distribution of surfactants of opposite charge in the bilayer.
引用
收藏
页码:4983 / 4990
页数:8
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