Importance of the Electrostatic Correlations in Surface Tension of Hydrated Reline Deep Eutectic Solvent from Combined Experiments and Molecular Dynamics Simulations

被引:1
|
作者
Cuvellier, Jean-Baptiste [1 ]
Andanson, Jean-Michel [2 ]
Ballerat-Busserolles, Karine [2 ]
Hulin, Hyazann [1 ]
Artzner, Franck [1 ]
Malfreyt, Patrice [2 ]
Ghoufi, Aziz [1 ,3 ]
机构
[1] Univ Rennes, CNRS, IPR Inst Phys Rennes, UMR 6251, F-35000 Rennes, France
[2] Univ Clermont Auvergne, CNRS, Inst Chim Clermont Ferrand, Clermont Auvergne INP, F-63000 Clermont Ferrand, France
[3] Univ Paris East Creteil, CNRS, ICMPE, UMR 7182, F-94320 Thiais, France
关键词
PRESSURE TENSOR; AQUEOUS-RELINE; WATER; LIQUID; MIXTURES; PERTURBATION; INTERFACE; AMMONIUM; DESS;
D O I
10.1021/acs.jpcb.3c08338
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, the surface tension and the structure of hydrated reline are investigated by using diverse methods. Initially, the surface tension displays a nonlinear pattern as water content increases, decreasing until reaching 45 wt %, then gradually matching that of pure water. This fluctuation is associated with strong electrostatic correlations present in pure reline, which decrease as more water is added. Changes in surface tension reflect a shift from charge layering in pure reline to an increased interfacial hydrogen bonding as the water content rises. This shift causes the segregation of urea molecules into the bulk phase and a gradual anchoring of water molecules to the air-reline interface. An interesting observation is the antisurfactant effect, where heightened interfacial anchoring results in an unexpected increase in real contribution of surface tension. This, along with weakened electrostatic correlations beyond 45 wt % due to reinforced interfacial hydrogen bonding, contributes to the complex behavior of surface tension observed in this study.
引用
收藏
页码:4008 / 4020
页数:13
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