Thermophysical properties of pure and water-saturated tetradecyltrihexylphosphonium-based ionic liquids

► Density and viscosity data of seven pure phosphonium ionic liquids are reported. ► Water content of saturated phosphonium ionic liquids is presented. ► Density and viscosity data of water-saturated ionic liquids are reported. ► Density data is only marginally affected by the presence of water. ► T...

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Bibliographic Details
Published in:The Journal of chemical thermodynamics 2011-06, Vol.43 (6), p.948-957
Main Authors: Neves, Catarina M.S.S., Carvalho, Pedro J., Freire, Mara G., Coutinho, João A.P.
Format: Article
Language:English
Subjects:
Bis(2,4,4-trimethylpentyl)phosphinate
Bis(trifluoromethylsulfonyl)imide
Bromide
Cations
Chemistry
Chloride
Chlorides
Correlation
Decanoate
Density
Dicyanamide
Exact sciences and technology
General and physical chemistry
Ionic liquids
Mathematical models
Methanesulfonate
Solubility
Solution properties
Solutions
Tetradecyltrihexylphosphonium
Thermophysical properties
Viscosity
Water
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Summary:► Density and viscosity data of seven pure phosphonium ionic liquids are reported. ► Water content of saturated phosphonium ionic liquids is presented. ► Density and viscosity data of water-saturated ionic liquids are reported. ► Density data is only marginally affected by the presence of water. ► The presence of water has a large impact in viscosities. In this work, the solubility of water in several tetradecyltrihexylphosphonium-based ionic liquids at 298.15 K, and densities and viscosities of both pure and water-saturated ionic liquids in a broad temperature range were measured. The selected ionic liquids comprise the common tetradecyltrihexylphosphonium cation combined with the following anions: bromide, chloride, bis(trifluoromethylsulfonyl)imide, decanoate, methanesulfonate, dicyanamide and bis(2,4,4-trimethylpentyl)phosphinate. The isobaric thermal expansion coefficients for pure and water-saturated ionic liquids were determined based on the density dependence with temperature. Taking into account that the excess molar volumes of the current hydrophobic water-saturated ionic liquids are negligible, the solubility of water was additionally estimated from the gathered density data and compared with the experimental solubilities obtained. Moreover, the experimental densities were compared with those predicted by the Gardas and Coutinho model while viscosity data were correlated using the Vogel–Tammann–Fulcher method.
ISSN:0021-9614
1096-3626
DOI:10.1016/j.jct.2011.01.016