Title of article :
Phase behaviour of 1-hexyloxymethyl-3-methyl-imidazolium and 1,3-dihexyloxymethyl-imidazolium based ionic liquids with alcohols, water, ketones and hydrocarbons: The effect of cation and anion on solubility
Author/Authors :
Doma?ska، نويسنده , , Urszula and Marciniak، نويسنده , , Andrzej، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
10
From page :
9
To page :
18
Abstract :
The liquid–liquid equilibrium (LLE), or solid–liquid equilibrium (SLE) of more than 20 binary systems containing 1-hexyloxymethyl-3-methyl-imidazolium bis(trifluoromethylsulfonyl)-imide [C6H13OCH2MIM][Tf2N] with alcohol (butan-1-ol, or hexan-1-ol, or octan-1-ol), water and ketone (3-pentanone, or cyclopentanone) and of 1-hexyloxymethyl-3-methyl-imidazolium tetrafluoroborate [C6H13OCH2MIM][BF4] with alcohol (methanol, or ethanol, or butan-1-ol, or hexan-1-ol, or octan-1-ol), water and ketone (3-pentanone, or cyclopentanone) have been measured. The solubility of dialkoxy-imidazolium salts: (1) 1,3-dihexyloxymethyl-imidazolium bis(trifluoromethylsulfonyl)-imide [(C6H13OCH2)2IM][Tf2N] in alcohol (butan-1-ol, or hexan-1-ol, or octan-1-ol, or decan-1-ol), in water and hydrocarbon (benzene, hexane and cyclohexane); (2) 1,3-dihexyloxymethyl-imidazolium tetrafluoroborate [(C6H13OCH2)2IM][BF4] in alcohol (hexan-1-ol, or octan-1-ol, or decan-1-ol) and water have been measured. Measurements were carried out by using a dynamic method from T = 275 K to the boiling point of the solvent. In this work a systematic study of the impact of different factors on the phase behaviour of hexyloxy-imidazolium-based ionic liquids with polar and nonpolar solvents has been presented. Most of the examined systems showed immiscibility in the liquid phase with an upper critical solution temperature (UCST), or complete solubility of the ionic liquid at room temperature in many solvents. An increase in the alkyl chain length of alcohol resulted in an increase in the UCST. The choice of anion was shown to have large impact on the solubility: by changing the anion [Tf2N]− to [BF4]−, the solubility dramatically decreased and the UCST increased. By contrast, increasing hydrogen bonding opportunities with the solvent by replacing a methyl group with the second alkoxy-group on the imidazolium ring results in an increase of the solubility. per includes also a thermophysical basic characterization of pure ionic liquids obtained via differential scanning calorimetry (TG/DSC), temperatures of decomposition and melting, enthalpies of fusion, enthalpies of solid–solid phase transitions and temperatures of the glass transition. perimental results of LLE and SLE have been correlated using the NRTL, or Wilson equations. The average root-mean square deviation of the equilibrium mole fraction for all the LLE data was 0.010 and average mean square deviation of temperature for SLE was 1.06 K. he solubility results the partition coefficient of ionic liquids in binary system octan-1-ol/water mixtures has been calculated. Experimental partition coefficients (log P) at the temperature 298.15 K were negative.
Keywords :
Solid–liquid equilibrium , Correlation , Octan-1-ol/water partition coefficients , Thermophysical properties , Ionic liquids , Liquid–liquid equilibrium , Hexyloxymethyl- and dihexyloxymethyl-imidazolium salts
Journal title :
Fluid Phase Equilibria
Serial Year :
2007
Journal title :
Fluid Phase Equilibria
Record number :
1986613
Link To Document :
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