Abstract

The paper presents new data on the activity coefficient at infinite dilution (γ13∞) for 29 various organic solutes: alkanes, alkenes, al-kynes, cycloalkanes, alcohols, ethers, ketones and aromatic hydrocarbons in two quaternary-ammonium based ionic liquids (quat-based ILs): didecyldimethylammonium perchlorate [DDA][ClO4] and didecyldimethylammonium tetrafluoroborate [DDA][BF4]. The activity coefficient at infinite dilution and physicochemical properties of two mentioned ionic liquids, were determined by inverse gas chromatography at four different temperatures: 308K, 323K, 338K and 353K. Additionally, on the basis of the specific retention volume (Vg0) the Flory – Huggins interaction parameters (χ∞) were determined. In order to identify the fundamental interaction between solute and solvent inside the column, the partial molar excess enthalpies at infinite dilution (ΔH1E,∞) were calculated on the basis of experimental γ13∞ values. The selectivity (Sij∞) and capacity (kj∞) at infinite dilution for a few different separation problems: hexane/benzene, cyclohexane/benzene and hexane/tetrahydrofuran were calculated from the experimental γ13∞ values to evaluate the possible use of the ionic liquids studied as a new class of solvents in liquid-liquid extraction and in other extraction or microextraction methods. The values of the above-mentioned parameters were compared and discussed taking into regard the chemical structures of both quaternary ammonium-based ionic liquids, including the same cation and their interactions with the organic solute.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.