While
a large amount of attention has been paid to investigating
the effects of various factors (e.g., solvent and asphaltene molecular
structure) on asphaltene adsorption, the effect of salinity, particularly
brine water, has not been systematically studied at the atomistic
level despite the ubiquitous presence of salt in crude oil processing.
In this work, the adsorption behaviors of a model asphaltene at the
oil/brine interface were investigated using molecular dynamics simulations.
It was found that the addition of salt greatly enhances the adsorption
kinetics in systems with a small droplet, while this enhancement was
insignificant for systems with a large droplet. Furthermore, dependent
on droplet size, salinity has different effects on the adsorbed structures.
In systems with a small droplet, the addition of ions facilitates
the direct contact of adsorbed model asphaltene molecules with water
surfaces, while in systems with a large droplet, such direct contact
was suppressed. Detailed analysis of hydrogen bonding, water/ion distributions,
and shape transformation of the water droplet suggests that these
observations result from the different degrees of hydration in systems
with small and large droplets: small droplets have large surface area
to volume ratio, and thus cannot facilitate strong ion hydrations,
while large droplets manifest strong ion hydrations, leading to reduced
model asphaltene and water attractions. The results reported here
can enhance our understanding of emulsification mechanisms in high-salinity
crude oil at an atomistic level.