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Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets
Published on: May 15, 2017
Structural transitions induced by shear flow and temperature variation in a nonionic surfactant/water system
Luigi Gentile1, Bruno F B Silva, Sandor Balog
1Department of Chemistry, University of Calabria, P. Bucci 14C, 87036 Rende, Italy. luigi.gentile@unical.it
Shear flow and temperature induce structural changes in tetraethylene glycol monohexadecyl ether (C(16)E(4)) solutions. A novel sponge phase emerges, coexisting with lamellar phases, showing unique behavior compared to shorter chain surfactants.
Area of Science:
- Materials Science
- Physical Chemistry
- Soft Matter Physics
Background:
- Nonionic surfactants like tetraethylene glycol monohexadecyl ether (C(16)E(4)) exhibit complex phase behavior.
- Understanding their structural transitions under external stimuli is crucial for applications.
Purpose of the Study:
- To investigate the structural transitions of C(16)E(4) in D(2)O under shear flow and varying temperatures.
- To compare the shear flow behavior of C(16)E(4) with other nonionic surfactants.
Main Methods:
- Rheology to measure flow properties.
- Rheo-small-angle neutron scattering (rheo-SANS) to probe nanoscale structures.
- Rheo-small-angle light scattering (rheo-SALS) to analyze larger structures.
Main Results:
- Competition between multi-lamellar vesicles, planar lamellae, and a sponge phase was observed.
- A new transient lamellar phase with increased spacing coexists with the initial lamellar phase in a narrow temperature-time window.
- The shear flow behavior of C(16)E(4) resembles that of longer chain surfactants (C(16)E(7)) rather than shorter ones (C(10)E(3), C(12)E(4)).
Conclusions:
- Shear flow and temperature are key factors driving structural evolution in C(16)E(4) solutions.
- The formation of a transient lamellar phase and its coexistence with other phases highlight complex self-assembly mechanisms.
- C(16)E(4) exhibits distinct shear-induced phase behavior influenced by its long alkyl chain length.
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