Evolution of a lamellar domain structure for an equilibrating lyotropic liquid crystal

被引:17
|
作者
Hubbard, Penny L. [1 ]
McGrath, Kathryn M. [1 ]
Callaghan, Paul T. [1 ]
机构
[1] Victoria Univ Wellington, Sch Chem & Phys Sci, MacDiarmid Inst Adv Mat & Nanotechnol, Wellington 6001, New Zealand
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2006年 / 110卷 / 42期
关键词
D O I
10.1021/jp0601872
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
Aerosol OT/water exhibits a lamellar phase over a wide range of concentrations. We show, by magnetic resonance (NMR) and scanning electron microscopy (SEM), that the morphology of the lamellar phase varies significantly across that range and that the rate of equilibration depends strongly on concentration (25, 33, and 50 wt %) with, paradoxically, the faster equilibration at higher surfactant concentrations. We find that the 25 wt % sample exhibits a defect-rich local structure, characteristic of a superposed L(3) character. Further into the lamellar region, at 33 wt %, this defect-rich structure persists heterogeneously, while, at 50 wt %, the lamellar phase domains are highly ordered. The NMR methods used here included (2)H spectroscopy and the two-dimensional NMR method, diffusion-diffusion exchange spectroscopy (DEXSY). The latter was used to obtain quantitative information on the domain sizes and defects within the polydomain lamellar mesophase. Comparison of the NMR with the SEM results suggests that, at 25 wt % AOT, bilayer defects play an important role in influencing the 2H NMR and DEXSY NMR results.
引用
收藏
页码:20781 / 20788
页数:8
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