TY - JOUR
T1 - Evidence for water ridges at oil-water interfaces
T2 - Implications for ion transport
AU - Wen, Boyao
AU - Sun, Chengzhen
AU - Zheng, Wenxiu
AU - Bai, Bofeng
AU - Lichtfouse, Eric
N1 - Publisher Copyright:
© 2020 The Royal Society of Chemistry.
PY - 2020
Y1 - 2020
N2 - Understanding ion transport across interfaces is of fundamental importance in many processes such as liquid-liquid extraction, phase transfer catalysis, enhanced oil recovery and emulsion stabilisation. However, the factors that control ion transport across interfaces are poorly known due to a lack of knowledge of structural changes at interfaces. We studied here the effects of ionic concentration and external force on the transport of ions across the decane-water interface using classical molecular dynamics simulations. The results show that the evolution of interfacial structures during ion transfer across the interface is controlled by hydrogen bonding and ionic interactions at the interface. We also identified a new mode of ion transfer across the interface at low ionic concentrations, involving a 'water ridge', rather that the classical 'water finger'. In the water ridge mode, hydrogen bonds are not broken due to low ion levels, and the water ridge induces gradual interface deformation. Whereas, at high ionic concentrations, hydrogen bonds are broken by the strong ion electrostatic repulsion, thus inducing the formation of a water finger. We also found that the variation of the Gibbs free energy during ion transfer is directly relevant to the ionic concentration. The water ridge at low ionic concentrations, which displaces more water molecules towards the decane phase, induces less free energy variation than the water finger at high ionic concentrations.
AB - Understanding ion transport across interfaces is of fundamental importance in many processes such as liquid-liquid extraction, phase transfer catalysis, enhanced oil recovery and emulsion stabilisation. However, the factors that control ion transport across interfaces are poorly known due to a lack of knowledge of structural changes at interfaces. We studied here the effects of ionic concentration and external force on the transport of ions across the decane-water interface using classical molecular dynamics simulations. The results show that the evolution of interfacial structures during ion transfer across the interface is controlled by hydrogen bonding and ionic interactions at the interface. We also identified a new mode of ion transfer across the interface at low ionic concentrations, involving a 'water ridge', rather that the classical 'water finger'. In the water ridge mode, hydrogen bonds are not broken due to low ion levels, and the water ridge induces gradual interface deformation. Whereas, at high ionic concentrations, hydrogen bonds are broken by the strong ion electrostatic repulsion, thus inducing the formation of a water finger. We also found that the variation of the Gibbs free energy during ion transfer is directly relevant to the ionic concentration. The water ridge at low ionic concentrations, which displaces more water molecules towards the decane phase, induces less free energy variation than the water finger at high ionic concentrations.
UR - https://www.scopus.com/pages/publications/85078526323
U2 - 10.1039/c9sm01791g
DO - 10.1039/c9sm01791g
M3 - 文章
C2 - 31840723
AN - SCOPUS:85078526323
SN - 1744-683X
VL - 16
SP - 826
EP - 832
JO - Soft Matter
JF - Soft Matter
IS - 3
ER -