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Paracrystal model of the high‐temperature lamellar phase of a ternary microemulsion system
Author(s) -
Kotlarchyk M.,
Ritzau S. M.
Publication year - 1991
Publication title -
journal of applied crystallography
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.429
H-Index - 162
ISSN - 1600-5767
DOI - 10.1107/s0021889890012213
Subject(s) - lamellar structure , paracrystalline , scattering , materials science , phase (matter) , lamellar phase , microemulsion , pulmonary surfactant , neutron scattering , microstructure , ternary operation , anisotropy , crystallography , analytical chemistry (journal) , molecular physics , optics , chemistry , thermodynamics , composite material , physics , chromatography , organic chemistry , programming language , computer science
Small‐angle neutron scattering was used to investigate the microstructure of the high‐temperature L α phase in the AOT/water/decane system [AOT = sodium bis(2‐ethylhexyl) sulfosuccinate]. The system was modeled as randomly oriented lamellar stacks with a one‐dimensional paracrystalline distortion. For samples injected into cells at high temperature, the two‐dimensional Q maps show anisotropic scattering consistent with partial alignment of the phase, while samples injected near room temperature do not exhibit this feature. From the latter samples, it was found that a stack typically contains about 15 lamellae, about 80 Å apart. Each layer is coated by a diffuse surfactant interface with a characteristic thickness of approximately 9 Å. The fact that the scattering spectra do not exhibit maxima beyond the first order is explained by the observation that the Hosemann g factor gives about a 20% variation in the interlamellar spacing. The mean spacing is inversely proportional to the surfactant concentration, as expected for a lamellar phase. Over‐estimation of the zero‐order scattering predicted by the paracrystal model is attributed primarily to improper treatment of the contrast between each layer and the space‐filling lamellar matrix.