It
is hypothesized that polymeric lignin surfactants have different
affinities for stabilizing oil–water emulsions and that the
emulsifying performance of these surfactants is highly affected by
their adsorption performance at the oil–water interface. To
validate this hypothesis, the adsorption performance of sulfethylated
lignin (SEKL) surfactant at different oil–water interfaces
was examined by assessing the contact angle, dynamic interfacial tension,
and surface loading (Γ). Moreover, the interfacial adsorption
kinetics of SEKL was comprehensively assessed in different oil–water
systems to reveal the mechanisms of the SEKL adsorption at the interface.
Also, the impacts of SEKL concentration and ionic strength on the
performance of SEKL as an effective emulsifier for the emulsions were
assessed. Furthermore, the droplet size and instability index of the
emulsions were systematically correlated with the adsorption performance
of SEKL at the interface of oil and water. For the first time, by
implementing a modified Ward Toradai diffusion model, two distinct
early stages of the adsorption of SEKL at the oil interface were identified.
Interestingly, the second stage was the determining stage of adsorption
with the diffusion-controlled mechanism when polymers reconfigured
at the oil–water interface. Salt screening facilitated the
clustering of SEKL upon charge repulsion elimination, which removed
the energy barrier in the first stage of adsorption (ΔE
p
→0 = 0),
but it introduced a steric barrier upon the reconfiguration of polymers
at the oil interfaces in the second stage of adsorption. In addition
to the kinetics of adsorption, satisfactory correlations were observed
between surface pressure (Δγ = γ∞ – γ0), surface loading (Γ) of polymers,
and contact angle at oil interfaces on one hand and the oil droplet
size and emulsion stability on the other hand.