Foams Stabilized by Tricationic Amphiphilic Surfactants
Seth Heerschap, John N. Marafino, Kristin McKenna, Kevin L. Caran and, Klebert Feitosa

TL;DR
This study investigates how the structure of tris-cationic amphiphilic surfactants influences their ability to produce and stabilize foam, revealing that tail length and number significantly affect foam stability and that CAC predicts foamability.
Contribution
It provides new insights into how specific molecular architectures of amphiphilic surfactants affect foam formation and stability, guiding design of more effective foam stabilizers.
Findings
Shorter double-tailed molecules produce very stable foams.
Foam stability correlates with lower gas permeability of the monolayer.
CAC is a good predictor of foamability and stability.
Abstract
The unique surface properties of amphiphilic molecules have made them widely used in applications where foaming, emulsifying or coating processes are needed. Novel surfactant architectures with multi-cephalic and multi-tailed molecules have reportedly enhanced their anti-bacterial activity in connection with tail length and the nature of the head group, but their ability to produce and stabilize foam is mostly unknown. Here we report on experiments with tris-cationic, triple-headed, double- and single-tailed amphiphiles and their foamability and foam stability with respect to head group, tail number and tail length. The amphiphiles are composed of an aromatic mesitylene core and three benzylic amonium bromide groups, with alkyl chains attached to one or two of the head groups. Whereas shorter (14 carbons in length) double-tailed molecules are found to produce very stable foams, foams…
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