HYPOTHESIS Stimuli-responsive surfactants (also known as switchable surfactants) can undergo reversible conversions between active and inactive forms under particular stimuli, affecting surface and interfacial activity, aggregation structure, emulsification and solubilisation.… Click to show full abstract
HYPOTHESIS Stimuli-responsive surfactants (also known as switchable surfactants) can undergo reversible conversions between active and inactive forms under particular stimuli, affecting surface and interfacial activity, aggregation structure, emulsification and solubilisation. Selenium-containing surfactants are of reversibly redox-responsive. Hence, microemulsions (MEs) stabilized by selenium-containing surfactants should reversibly respond to redox reactions. EXPERIMENTS The formation of MEs, consisting of sodium dodecylselanylpropyl sulfate (reduced form, SDSePS-Re) or its oxidized form (SDSePS-Ox), n-butanol, n-heptane, and water, was verified based on a pseudo-ternary phase diagram. Changes in molecular structure between SDSePS-Re and SDSePS-Ox were verified by nuclear magnetic resonance spectrometry and electrospray ionization mass spectrometry. The transition between SDSePS-Re- and SDSePS-Ox -based MEs was systematically characterized through electrical conductivity measurements, cryo-transmission electron microscopy and dynamic light-scattering. FINDINGS Both SDSePS-Re and SDSePS-Ox could stabilize the mixture of n-butanol-n-heptane-water to form MEs. A reversible transition between an SDSePS-Re-based ME and the corresponding SDSePS-Ox-based ME was achieved, which was realized by the oxidation of SDSePS-Re with H2O2 and then reduction with N2H4. Compared with SDSePS-Re, SDSePS-Ox has a lower surface activity, resulting in a difference in solubilization capacity of the oil between SDSePS-Re- and SDSePS-Ox -based MEs. After oxidation with H2O2, phase separation could be observed in some SDSePS-Re-based MEs; however, the SDSePS-Re-based MEs could be recovered after reduction of SDSePS-Ox-based MEs with N2H4.
               
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