Thermophysical properties and phase equilibria study of the binary systems {N-hexylquinolinium bis(trifluoromethylsulfonyl)imide plus aromatic hydrocarbons, or an alcohol}

被引:28
作者
Domanska, Urszula [1 ,2 ]
Zawadzki, Maciej [1 ]
Zwolinska, Magdalena [3 ]
机构
[1] Warsaw Univ Technol, Dept Phys Chem, Fac Chem, PL-00664 Warsaw, Poland
[2] Univ KwaZulu Natal, Sch Chem Engn, Thermodynam Res Unit, ZA-4001 Durban, South Africa
[3] Cent Inst Labour Protect Natl Res Inst, Lab Thermal Loads, Dept Ergon, PL-00701 Warsaw, Poland
关键词
HQuin][NTf2; Density; viscosity; heat capacity; Binary solid or (liquid plus liquid) phase equilibria diagrams; Correlation; Thermodynamics; IONIC LIQUIDS; SEPARATION; SELECTION; BEHAVIOR;
D O I
10.1016/j.jct.2010.12.021
中图分类号
O414.1 [热力学];
学科分类号
摘要
The new quinolinium ionic liquid has been synthesised as a continuation of our work with quinolinium-based ionic liquids (ILs). The work includes specific basic characterisation of synthesized compounds: N-hexylquinolinium bromide, [HQuin][Br] and N-hexylquinolinium bis{(trifluoromethyl)sulfonyl}imide [HQuin][NTf2] by NMR spectra, elementary analysis and water content. The basic thermal properties of the pure [HQuin][NTf2] i.e. melting and glass-transition temperatures, the enthalpy of fusion as well as heat capacity have been measured using a differential scanning microcalorimetry technique (DSC) and thermal analysis instrument (TA). Densities and viscosities were determined as a function of temperature. Phase equilibria for the binary systems: {[HQuin][NTf2]) + aromatic hydrocarbon (benzene, or toluene, or ethylbenzene, or n-propylbenzene), or an alcohol (1-butanol, or 1-hexanol, or 1-octanol, or 1-decanol)} have been determined at ambient pressure. A dynamic method was used over a broad range of mole fractions and temperatures from (270 to 320) K. For all the binary systems with benzene and alkylbenzenes, the eutectic diagrams were observed with immiscibility gap in the liquid phase beginning from (0.13 to 0.28) mole fraction of the IL with very high an upper critical solution temperature (UCST). For mixtures with alcohols, the complete miscibility was observed for 1-butanol and immiscibility with UCST in the liquid phase for the remaining alcohols. The typical dependence was observed, that with increasing chain length of an alcohol the solubility decreases. The well-known NRTL equation was used to correlate experimental (solid + liquid), SLE and (liquid + liquid), LLE phase equilibria data sets. For the systems containing immiscibility gaps, (IL + an alcohol) parameters of the LLE correlation were used to the prediction of SLE. (C) 2011 Elsevier Ltd. All rights reserved.
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页码:775 / 781
页数:7
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