Thermophysical properties of ionic liquid {1-butyl-3-methylimidazolium bromide [bmim][Br] in alkoxyalkanols plus water} mixtures at different temperatures

被引:14
|
作者
Pal, Amalendu [1 ]
Kumar, Harsh [2 ]
Kumar, Bhupinder [1 ]
Sharma, Pooja [2 ]
Kaur, Kirtanjot [2 ]
机构
[1] Kurukshetra Univ, Dept Chem, Kurukshetra 136119, Haryana, India
[2] Dr B R Ambedkar Natl Inst Technol, Dept Chem, Jalandhar 144011, Punjab, India
来源
关键词
Ionic liquid; Alkoxyalkanols; Apparent molar volume; Adiabatic compressibility; Transfer volume; Apparent molar expansivity; SOLVENT-FREE ROUTE; VOLUMETRIC PROPERTIES; PHYSICAL-PROPERTIES; AQUEOUS-SOLUTIONS; AMINO-ACIDS; EXPANSIBILITIES; ELECTROLYTE; CATALYSIS; CAPTURE; SYSTEM;
D O I
10.1016/j.jct.2012.08.023
中图分类号
O414.1 [热力学];
学科分类号
摘要
The interactions of alkoxyalkanols with the ionic liquid 1-butyl-3-methylimidazolium bromide [bmim][Br] as a function of temperature were investigated by combination of volumetric and acoustic methods. The density, rho, and speed of sound, u, of ethylene glycol monomethyl ether, diethylene glycol monomethyl ether, and triethylene glycol monomethyl ether (0.00-1.01 mol.kg(-1)) in aqueous 1-butyl-3-methylimidazolium bromide solutions ranging from pure water to 0.29 mass% of ionic liquid have been measured at T = (288.15, 298.15 and 308.15) K and atmospheric pressure. The apparent molar volume (V-phi) and adiabatic compressibility (K-phi,K-S) of alkoxyalkanols in aqueous ionic liquid solution were determined at the measured temperatures. The partial molar volume (V-phi(0)) and partial molar adiabatic compressibility dK0 u_ of alkoxyalkanols at infinite dilution were evaluated. Transfer volumes (Delta V-phi(0)) and transfer adiabatic compressibility (Delta(0)(E)) at infinite dilution from water to aqueous ionic liquid solution were also calculated. The temperature dependence of the apparent molar volume was used to calculate apparent molar expansivity (phi(0)(E)) and the Hepler's constant values, (partial derivative V-2(phi)0/partial derivative T-2). The results were explained on the basis of competing patterns of interactions of co-solvent and the solute. (C) 2012 Elsevier Ltd. All rights reserved.
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收藏
页码:182 / 188
页数:7
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