When the electric field strength (E)
surpasses
a certain threshold, secondary droplets are generated during the coalescence
between water droplets in oil and the oil–water interface (so-called
the droplet-interface partial coalescence phenomenon), resulting in
a lower efficiency of droplet electrocoalescence. This study employs
molecular dynamics (MD) simulations to investigate the droplet-interface
partial coalescence phenomenon under direct current (DC) electric
fields. The results demonstrate that intermolecular interactions,
particularly the formation of hydrogen bonds, play a crucial role
in dipole–dipole coalescence. Droplet-interface partial coalescence
is categorized into five regimes based on droplet morphology. During
the contact and fusion of the droplet with the water layer, the dipole
moment of the droplet exhibits alternating increases and decreases
along the electric field direction. Electric field forces acting on
sodium ions and the internal interactions within droplets promote
the process of droplet-interface partial coalescence. High field strengths
cause significant elongation of the droplet, leading to its fragmentation
into multiple segments. The migration of hydrated ions has a dual
impact on the droplet-interface partial coalescence, with both facilitative
and suppressive effects. The time required for droplet-interface partial
coalescence initially decreases and subsequently increases as the
field strength increases, depending on the competitive relationship
between the extent of droplet stretching and the electric field force.
This work provides molecular insights into the droplet-interface coalescence
mechanisms in water-in-oil emulsions under DC electric fields.