Oscillating reactions often employed to mimic and understand complex dynamics in biological systems are known to be affected in aggregated host environments. The dynamic evolution of the oscillatory Belousov–Zhabotinsky (BZ) reaction upon addition of increasing amounts of anionic (sodium dodecylbenzenesulfonate; SDBS), cationic (hexadecyltrimethylammonium bromide; CTAB), nonionic (polyoxyethylene(20) cetyl ether; Brij58), and binary mixtures (CTAB + Brij58 and SDBS + Brij58) of surfactants was monitored using potentiometry at 25 and 35°C under stirred batch conditions. The experimental results reveal that the oscillatory parameters of the Ce(IV)‐catalyzed BZ reaction are significantly altered depending on the concentration and nature of restricted micellar host environments. In the presence of ionic surfactants, it is proposed that the evolution of the oscillatory BZ system may be due to atypical proficiency (related to hydrophobic and electrostatic interactions) of such organized self‐assemblies to affect the reactivity by selectively confiscating some key reacting species. However, the response of the BZ system to nonionic Brij58 was attributed to the reaction among the alcoholic functional groups of the surfactant with some vital species of the BZ reaction. Moreover, the nonionic + ionic binary surfactant systems exhibited behaviors representative of both the constitutive single surfactant systems.
The bulk and interfacial shear rheological behavior of aqueous solutions of biocompatible polymer HPC has been investigated in the presence of cationic CTAB and nonionic Tween 40 having the same chain length but different head groups. Steadystate bulk experiments depict two distinct regions in the rheogram (Newtonian followed by pseudoplastic). Dynamic experiments suggest that the stability of HPC hydrogels decreases with the increase in surfactant concentration. Interfacial steady shear tests of 2D monolayers of 1 wt % HPC and 1 wt % HPC with varying concentrations of Tween 40/CTAB show a non-Newtonian dilatant behavior at the solution−air interface. However, two distinct dilatant regions separated by a Newtonian region were observed for the same films at the solution−soya oil interface. The strength of films formed at the two interfaces decreases with the increase of surfactant concentration as observed from oscillatory interfacial tests. HPC interacts more strongly with CTAB than Tween 40 both in bulk as well as at the interfaces studied.
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