화학공학소재연구정보센터
Electrochimica Acta, Vol.80, 196-201, 2012
Ion association constants of ionic liquids, 1-hexyl-3-methylimidazolium halide, in aqueous D-fructose solutions
In this paper, the interactions of 1-hexyl-3-methylimidazolium halides ([HMIm]Cl and [HMIm]Br) with aqueous El-fructose solutions have been studied by using conductance properties. Limiting molar conductivity (Lambda(0)), association constant (K-A)and distance parameter (R) were calculated using low concentration Chemical Model (IcCM) at temperatures ranges of (298.15-328.15)K and concentrations (0.05, 0.10 and 0.20) mol kg(-1) of D-fructose solutions. The Lambda(0) values increase with increasing temperature and decrease during the addition of D-fructose. The greater values of association constant for [HMIm]Cl relative to [HMIm]Br is due to the high surface charge density of the Cl- anion proposing strong association tendency with [HMIm](+) cation. Moreover, an enhancement was observed in the K-A values as temperature is increased suggesting that ion-pair formation is an endothermic process. The mobility of ions was found to be completely controlled by the bulk viscosity (eta) and consequently the Walden products (Lambda(0)eta) were estimated and discussed. The association constants were used to study the thermodynamic of association process. Consequently, Gibbs free energy (Delta G(A)(0)), enthalpy (Delta H-A(0)) and entropy (Delta S-A(0)) of ion-pair formation have been obtained at different temperatures. It was observed that the ion-association process exhibits a negative value of Delta G(A)(0), and becomes more negative with increasing temperature proposing the spontaneity and feasibility of the association at high temperatures. (C) 2012 Elsevier Ltd. All rights reserved.