Surfactants
are often added to aqueous solutions to induce spreading
on otherwise unwettable hydrophobic surfaces. Alternatively, they
can be introduced directly into solid hydrophobic materialssuch
as the soft elastomer, polydimethylsiloxaneto induce autonomous
wetting without requiring additional surface or liquid modifications.
Given the similarity between mechanisms of these two approaches, models
that describe wetting by aqueous surfactant solutions should also
characterize wetting on surfactant–solid systems. To investigate
this theory, multiple surfactants of varying size and chemical composition
were added to prepolymerized PDMS samples. After cross-linking, water
droplets were placed on the surfaces at set time points, and their
contact angles were recorded to track the temporal evolution of the
interfacial tension. Multiple nonlinear models were fitted to this
data, their parameters were analyzed, and each goodness of fit was
compared. An empirical model of dynamic surface tension was found
to describe the wetting process better than the single established
model found in the literature. The proposed model adapted better to
the longer time scales induced by slow molecular diffusivity in PDMS.
Siloxane ethoxylate surfactants induced faster and more complete wetting
of PDMS by water than oxyoctylphenol ethoxylates did. The generalizability
of this model for characterizing nonionic surfactants of a wide range
of physiochemical properties was demonstrated.