How the cation 1-butyl-3-methylimidazolium impacts the interaction between the entrapped water and the reverse micelle interface created with an ionic liquid-like surfactant

被引:42
|
作者
Lepori, Cristian M. O. [1 ]
Mariano Correa, N. [1 ]
Silber, Juana J. [1 ]
Dario Falcone, R. [1 ]
机构
[1] Univ Nacl Rio Cuarto, Dept Quim, Agencia Postal 3,CP X5804BYA, Rio Cuarto, Argentina
关键词
DYNAMIC LIGHT-SCATTERING; IN-OIL MICROEMULSIONS; AEROSOL-OT; FT-IR; AQUEOUS-SOLUTION; ENZYMATIC CATALYSIS; 2-NAPHTHYL ACETATE; SOLUBILIZED WATER; ENERGY-TRANSFER; POLAR-SOLVENTS;
D O I
10.1039/c5sm02421h
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
The behavior of the interfacial water entrapped in reverse micelles (RMs) formed by the ionic liquid-like surfactant 1-butyl-3-methylimidazolium 1,4-bis-2-ethylhexylsulfosuccinate (bmim-AOT) dissolved in benzene (or chlorobenzene) was investigated using noninvasive techniques such as dynamic light scattering (DLS), static light scattering (SLS), FT-IR and H-1 NMR. The DLS and SLS results reveal the formation of discrete spherical and non-interacting water droplets stabilized by the bmim-AOT surfactant. Moreover, since the droplet size increases as the W-0 (W-0 = [water]/[surfactant]) value increases, water interacts with the RM interface. From FT-IR and H-1 NMR data, a weaker water-surfactant interaction in bmim-AOT RMs in comparison with the RMs created by sodium 1,4-bis-2-ethylhexylsulfosuccinate (Na-AOT) is detected. Consequently, there are less water molecules interacting with the interface in bmim-AOT RMs, and their hydrogen bond network is not completely disrupted as they are in Na-AOT RMs. The results show how the nature of the new cation impacts the interaction between the entrapped water and the RM interface, modifying the interfacial water structure in comparison with the results known for Na-AOT.
引用
收藏
页码:830 / 844
页数:15
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