Thermodynamic and transport properties of ionic liquids, 1-alkyl-3-methylimidazolium thiocyanate in the aqueous lithium halides solutions

[Display omitted] •Some thiocyanate based ILs, [RMIM][SCN], were synthesized.•Thermophysical properties of aqueous solutions of LiX + ILs were studied.•SPT was used to found out interaction’s changes between IL and H2O.•Structural effects of LiX and [RMIM][SCN] on solvation properties were discussed...

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Veröffentlicht in:The Journal of chemical thermodynamics 2020-02, Vol.141, p.105953, Article 105953
Hauptverfasser: Shekaari, Hemayat, Taghi Zafarani-Moattar, Mohammed, Golmohammadi, Behrang
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Sprache:eng
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Zusammenfassung:[Display omitted] •Some thiocyanate based ILs, [RMIM][SCN], were synthesized.•Thermophysical properties of aqueous solutions of LiX + ILs were studied.•SPT was used to found out interaction’s changes between IL and H2O.•Structural effects of LiX and [RMIM][SCN] on solvation properties were discussed. Thiocyanate based ionic liquids, [RMIM][SCN], as fluorine free and low toxic were used effectively in different areas of resaerch. In this work, the thermodynamic and transport properties of aqueous solutions of the synthesized ionic liquids based on thiocyanate anion, [RMIM][SCN] (R = butyl, hexyl and octyl) have been investigated at T = (288.15–318.15) K. Also, effect of LiX (X = Cl−, Br−) salts on the investigated properties have been studied at T = 298.15 K. In this respect, density, speed of sound and viscosity of the solutions have been measured and these properties were used to calculate the apparent molar volume, Vφ, and apparent molar isentropic compressibility κφ. The properties were correlated with corresponding empirical relations to achieve standard partial molar volume, Vφ0, partial molar isentropic compressibility, κφ0, and viscosity B-coefficient. These parameters were used to analysis of the interactions between components. In order to separate Vφ0 contributions of the ILs in binary solutions, the scaled particle theory was used at T = (288.15–318.15) K. The results show that the hydrophobic hydration interactions are dominant interactions.
ISSN:0021-9614
1096-3626
DOI:10.1016/j.jct.2019.105953