Densities and Derived Thermodynamic Properties of Imidazolium-, Pyridinium-, Pyrrolidinium-, and Piperidinium-Based Ionic Liquids
In the present work, experimental density measurements are reported along with the derived thermodynamic properties, such as the isothermal compressibility (κ T ), the isobaric expansivity (α p ), and the thermal pressure coefficient (γ v ) for imidazolium-, pyridinium-, pyrrolidinium-, and piperidi...
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Published in: | Journal of chemical and engineering data Vol. 53; no. 3; pp. 805 - 811 |
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Main Authors: | , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Washington, DC
American Chemical Society
01-03-2008
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Subjects: | |
Online Access: | Get full text |
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Summary: | In the present work, experimental density measurements are reported along with the derived thermodynamic properties, such as the isothermal compressibility (κ T ), the isobaric expansivity (α p ), and the thermal pressure coefficient (γ v ) for imidazolium-, pyridinium-, pyrrolidinium-, and piperidinium-based ionic liquids (ILs), namely, 1-ethyl-3-methylimidazolium trifluoromethanesulfonate [C2mim][CF3SO3], 3-methyl-1-propylpyridinium bis(trifluoromethylsulfonyl)imide [C3mpy][NTf2], 1-methyl-1-propylpyrrolidinium bis(trifluoromethylsulfonyl)imide [C3mpyr][NTf2], 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide [C4mpyr][NTf2], and 1-methyl-1-propylpiperidinium bis(trifluoromethylsulfonyl)imide [C3mpip][NTf2] in the pressure (0.10 < P/MPa < 35.00) and temperature (293.15 < T/K < 393.15) domains. These ILs were chosen to provide an understanding of the influence of the cation and anion on the properties under study. Experimental densities are correlated with the Tait equation with an average absolute relative deviation (AARD) better than 0.02 %. It is shown that experimental densities are in good agreement with the densities obtained by the predictive method previously proposed by us. |
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Bibliography: | ark:/67375/TPS-ZFV43T4S-Z An additional three tables. This material is available free of charge via the Internet at http://pubs.acs.org. This work was supported by Fundação para a Ciência e a Tecnologia (Project POCI/EQU/58152/2004). R. L. Gardas and M. G. Freire acknowledge the financial support from Fundação para a Ciência e a Tecnologia through, respectively, their postdoctoral (SFRH/BPD/23246/2005) and PhD. (SFRH/BD/14134/2003) scholarships. istex:1F2F8BCD163D0A88D59F5B37F1F95D969317E66C |
ISSN: | 0021-9568 1520-5134 |
DOI: | 10.1021/je700670k |