Geometric features in lyotropic liquid crystalline phase transitions observed in aqueous surfactant systems

Abstract

Lyotropic liquid crystalline phases are widely known to be formed in aqueous surfactant mixtures. Although the phase behavior of several surfactants has been elucidated in the past years, a striking absence of detailed discussion on how molecular geometric parameters vary as different liquid crystals are formed is consistently seen in literature. The current work aimed to partially fill this gap, by determining how several structural parameters changed in a variety of phase transitions previously observed in aqueous surfactant binary and ternary mixtures. The main findings reveal that the cell parameter dimensions are strongly correlated with the packing fraction of small aggregates in each phase; the folding and interpenetration of surfactant hydrocarbon chains are most likely to happen in phases with lower curvature, and can greatly affect other structural parameters; added components can alter the aqueous surfactant phase behavior at different extents; and highly ordered phases are favored by a substantial decrease in the cross-sectional areas per surfactant; among others. The obtained results enable important knowledge on lyotropic liquid crystal formation, in addition to providing detailed information on how to control and obtain such phases, thus prospecting new insights in areas where they are highly desired.

Graphical Abstract

Keywords:

• Lyotropic liquid crystal
• surfactant
• self-assembly
• phase behavior
• structural parameter

Acknowledgments

Professor Watson Loh and IQ-UNICAMP are gratefully acknowledged for providing the infrastructure needed for obtaining data of (C₁₈)₂DMABr/water system.^[30]

Disclosure statement

No potential conflict of interest was reported by the author.

Correction Statement

This article has been republished with minor changes. These changes do not impact the academic content of the article.