Pressure, isotope, and water co-solvent effects in liquid-liquid equilibria of (ionic liquid plus alcohol) systems

被引:151
作者
Najdanovic-Visak, V
Esperança, JMSS
Rebelo, LPN
da Ponte, MN
Guedes, HJR
Seddon, KR
de Sousa, HC
Szydlowski, J
机构
[1] Univ Nova Lisboa, Inst Tecnol Quim & Biol, P-2780901 Oeiras, Portugal
[2] Univ Nova Lisboa, FCT, Dept Quim, REQUIMTE, P-2829516 Caparica, Portugal
[3] Queens Univ Belfast, QUILL Ctr, Belfast BT9 5AG, Antrim, North Ireland
[4] Univ Coimbra, FCT, Dept Engn Quim, P-3030290 Coimbra, Portugal
[5] Univ Warsaw, Dept Chem, PL-02089 Warsaw, Poland
关键词
D O I
10.1021/jp034576x
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Liquid-liquid phase splitting in ternary mixtures that contain a room-temperature ionic liquid and an alcohol aqueous solution-namely, [bmim] [PF6] + ethanol + water and [bmim] [NTf2] + 2-methylpropanol + water-is studied. Experimental cloud-point temperatures were obtained up to pressures of 400 bar, using a He-Ne laser light-scattering technique. Although pressurization favors mutual miscibility in the presence of high concentrations of alcohols, the contrary occurs in water-rich solutions. Both ternary mixtures exhibit a very pronounced water-alcohol co-solvent effect. Solvent isotope effects are also investigated. Phase diagrams are discussed using a phenomenological approach based on a "polymer-like" G(E) model coupled with the statistical-mechanical theory of isotope effects. The combined effect of a red shift of -15 cm(-1) for the O-H deformation mode of ethanol with a blue shift of +35 cm(-1) for the O-H stretching mode, both of which occurring after liquid infinite dilution in the ionic liquid, rationalizes the observed isotope effect in the phase diagram. Predicted excess enthalpy (H-E) values are inferred from the model parameters. Furthermore, using the Prigogine-Defay equation, an estimation of the excess volumes (V-E) is obtained.
引用
收藏
页码:12797 / 12807
页数:11
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