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Neutron Reflectometry of an Anionic Surfactant at the Solid-Liquid Interface under Shear
Rebecca J L Welbourn1, Felicity Bartholomew1, Philipp Gutfreund2
1BP Institute and Department of Chemistry, University of Cambridge , Madingley Rise, Madingley Road, Cambridge, U.K.
Langmuir : the ACS Journal of Surfaces and Colloids
|May 23, 2017
Summary
Shear forces disrupt the structure of adsorbed anionic surfactant multilayers at the alumina-water interface. Single bilayers, however, remain stable under these conditions, revealing distinct responses to applied stress.
Area of Science:
- Surface science and colloid chemistry
- Materials science
- Rheology
Background:
- Understanding interfacial surfactant behavior is crucial for applications like enhanced oil recovery, detergency, and nanoparticle stabilization.
- Anionic surfactants, such as sodium bis(2-ethylhexyl) sulfosuccinate (AOT), form complex structures at interfaces, influencing interfacial properties.
- The mechanical response of adsorbed surfactant layers under shear is not fully understood, particularly the transition from simple to complex structures.
Purpose of the Study:
- To investigate the shear response of adsorbed anionic surfactant layers at the alumina-water interface using combined neutron reflectometry and in situ rheology.
- To differentiate the structural stability of a single surfactant bilayer versus a multilamellar phase under varying shear conditions (steady and oscillatory).
- To elucidate the influence of strain amplitude on the structural integrity of adsorbed surfactant layers.
Main Methods:
- Utilized neutron reflectometry to probe the structure of adsorbed sodium bis(2-ethylhexyl) sulfosuccinate (AOT) at the alumina-water interface.
- Integrated in situ rheology to apply controlled shear (steady and oscillatory) to the interfacial surfactant layers during neutron reflectometry measurements.
- Analyzed structural changes in response to varying surfactant concentrations and applied shear parameters (shear rate, strain amplitude).
Main Results:
- At low AOT concentration, a stable single bilayer adsorbed at the interface, showing no structural changes under steady or oscillatory shear.
- At higher AOT concentration, a multilamellar surfactant structure formed, which exhibited a significant loss of structural order under both steady and oscillatory shear.
- The disruption of the multilamellar phase was dependent on strain amplitude, with distinct differences observed between steady and oscillatory shear responses.
Conclusions:
- The mechanical stability of adsorbed surfactant layers is highly dependent on their structural organization.
- Multilamellar surfactant phases are susceptible to shear-induced structural breakdown, unlike stable single bilayers.
- Neutron reflectometry coupled with in situ rheology provides a powerful tool for characterizing the dynamic response of interfacial surfactant structures.
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