1-Ethyl-3-methylimidazolium Ethylsulfate in Water, Acetonitrile, and Dichloromethane: Molar Conductivities and Association Constants

被引:65
作者
Bester-Rogac, Marija [1 ]
Hunger, Johannes [2 ]
Stoppa, Alexander [2 ]
Buchner, Richard [2 ]
机构
[1] Univ Ljubljana, Fac Chem, SI-1000 Ljubljana, Slovenia
[2] Univ Regensburg, Inst Phys & Theoret Chem, D-93040 Regensburg, Germany
关键词
ION-PAIR FORMATION; ELECTRICAL-CONDUCTIVITY; LIQUIDS; MIXTURES; CONDUCTANCE; VISCOSITY; CHLORIDE; DENSITY;
D O I
10.1021/je101130e
中图分类号
O414.1 [热力学];
学科分类号
摘要
Molar conductivities, Lambda, of dilute solutions of the ionic liquid 1-ethyl-3-methylimidazolium ethylsulfate in water, acetonitrile (AN), and dichloromethane (DCM) were determined as a function of temperature (AN: T = (273.15 to 313.15) K; DCM: T = (273.15 to 308.15) K; water: T = (278.15 to 313.15) K) in the concentration range c = (approximate to 0.25 to approximate to 5).10(-3) mol.dm(-3). The data were analyzed with Barthel's low-concentration chemical (lcCM) model to obtain the limiting molar conductivities, Lambda(infinity)(T), and association constants, K-A(circle)(T), of this electrolyte in the investigated solvents. From Lambda(infinity)(T) the Eyring activation enthalpy of charge transport was determined and found to be slightly larger than the corresponding value for viscous flow of the solvent. Strong ion pairing was found for the electrolyte in DCM (K-A(circle) approximate to 6.10(4) mol(-1).dm(3)), whereas ion association in AN is rather weak (K-A(circle) approximate to 40 mol(-1).dm(3)). From the temperature dependence of K-A(circle)(T) the enthalpy and entropy of the ion-pairing process were calculated, and ion association was found to be entropy-driven for both nonaqueous solvents. In water the salt is fully dissociated.
引用
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页码:1261 / 1267
页数:7
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