Activity Coefficients at Infinite Dilution and Physicochemical Properties for Organic Solutes and Water in the Ionic Liquid 1-Ethyl-3-methylimidazolium trifluorotris(perfluoroethyl)phosphate

New data of activity coefficients at infinite dilution, γ 13 ∞ , for 65 different solutes including alkanes, alkenes, alkynes, cycloalkanes, aromatic hydrocarbons, alcohols, thiophene, ethers, ketones, aldehydes, esters and water in the ionic liquid 1-ethyl-3-methylimidazolium trifluorotris(perfluor...

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Published inJournal of solution chemistry Vol. 44; no. 3-4; pp. 413 - 430
Main Authors Wlazło, Michał, Marciniak, Andrzej, Letcher, Trevor M.
Format Journal Article
LanguageEnglish
Published New York Springer US 01.04.2015
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Summary:New data of activity coefficients at infinite dilution, γ 13 ∞ , for 65 different solutes including alkanes, alkenes, alkynes, cycloalkanes, aromatic hydrocarbons, alcohols, thiophene, ethers, ketones, aldehydes, esters and water in the ionic liquid 1-ethyl-3-methylimidazolium trifluorotris(perfluoroethyl)phosphate, were determined using inverse gas chromatography within the temperature range from 318.15 to 368.15 K. This is a continuation of our study of ionic liquids based on this anion. The results are compared with the other trifluorotris(perfluoroethyl)phosphate ionic liquids. The γ 13 ∞ values were used to calculate thermodynamic functions such as partial molar excess Gibbs energies Δ G 1 E, ∞ , enthalpies Δ H 1 E, ∞ and entropies Δ S 1 E, ∞ as well as gas–liquid partition coefficients of the solutes, K L . These values were used to determine the linear free energy relationship (LFER) system constants as a function of temperature. The selectivities at infinite dilution needed for some extraction problems were calculated and compared with literature data of ionic liquids based on the trifluorotris(perfluoroethyl)phosphate anion and the 1-ethyl-3-methylimidazolium cation. Additionally, the density and viscosity of the investigated ionic liquid at temperatures from 298.15 to 348.15 K were measured.
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ISSN:0095-9782
1572-8927
DOI:10.1007/s10953-014-0274-0