posted on 2020-01-23, 15:03authored byZhidan Jia, Zhen Niu, Ziqi Yang, Xingang Li, Junyan Wang, Xiao He, Hong Sui, Lin He
The
ionic liquids (ILs) are reported to perform well in enhancing
the oil–solid separation (in pure state or in solution) and
oil–water separation (in solution) processes through interfacial
alteration. Herein, the interfacial behaviors of IL ([C8mim][Br], [C10mim][Br], and [C12mim][Br]) cations
and asphaltenes (from Indonesian asphalt) at the oil–water
interface have been investigated through dynamic and equilibrium characterizations.
The dynamic interfacial tensions (DIFTs) of toluene–water systems
with and without the addition of ILs and asphaltenes are measured.
It is found that both IL cations and asphaltenes could diffuse from
bulk solution to the oil–water interface quickly, resulting
in a competitive adsorption and accumulation at the interface. The
IL cations show faster diffusion ability and stronger interfacial
adsorbability compared with the asphaltenes. The π-A isotherms and atomic force microscopy (AFM) surface probing of the
spreading protocol and the diffusion protocol show that the IL cations
could protect the formation of a continuous cross-network, destroying
the interfacial asphaltene film. There is also evidence that the efficiency
of the interfacial alteration by IL cations is highly dependent on
IL cation type. The above results are further understood by the COSMOthermX
simulation. These findings suggest that the IL cations show stronger
dynamic diffusion and interfacial adsorption properties compared with
asphaltenes.