Multicomponent
heterogeneous systems containing volatile amphiphiles
are relevant to the fields ranging from drug delivery to atmospheric
science. Research presented here discloses the individual interfacial
activity and adsorption–evaporation behavior of amphiphilic
aroma molecules at the liquid–vapor interface. The surface
tension of solutions of nonmicellar volatile surfactants linalool
and benzyl acetate, fragrances as such, was compared with that of
the conventional surfactant sodium dodecyl sulfate (SDS) under equilibrium
as well as under no instantaneous equilibrium, including a fast-adsorbing
regime. In open systems, the increase in the surface tension on a
time scale of ∼10 min is evaluated using a phenomenological
model. The derived characteristic mass transfer constant is shown
to be specific to both the desorption mechanism and the chemistry
of the volatile amphiphile. Fast-adsorbing behavior disclosed here,
as well as the synergetic effect in the mixtures with conventional
micellar surfactants, justifies the advantages of volatile amphiphiles
as cosurfactants in dynamic interfacial processes. The demonstrated
approach to derive specific material parameters of fragrance molecules
can be used for an application-targeted selection of volatile cosurfactants,
e.g., in emulsification and foaming, inkjet printing, microfluidics,
spraying, and coating technologies.