Chem. J. Chinese Universities

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Studies on the Enthalpy of Solution of Ionic Liquid [C2mim][FeCl4] Based on Transition Metal

ZHANG Zi-Fu1, WANG Heng1, FANG Da-Wei1,2, YANG Jia-Zhen1*   

  1. 1. College of Chemistry, Liaoning University, Shenyang 110036, China;2. The Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China
  • Received:2007-07-12 Revised:1900-01-01 Online:2008-03-10 Published:2008-03-10
  • Contact: YANG Jia-Zhen

Abstract: A brown and transparent ionic liquid,[C2mim][FeCl4], was prepared by mixing anhydrous FeCl3 with 1-methyl-3-ethylimidazolium chloride([C2mim][Cl]), with molar ratio 1∶1 under stirring in a glove box filled with dry argon. The molar enthalpies of solution, ΔsHm, of [C2mim][FeCl4] in water with various molalities were determined by a solution-reaction isoperibol calorimeter at 298.15 K. In terms of Pitzer electrolyte solution theory, the standard molar solution enthalpy of [C2mim][FeCl4], ΔsH0m, and the sum of Pitzer parameters: (β(0)LFe,Cl+β(0)L[C2min],Cl+ΦLFe,[C2min]) and (β(1)LFe,Cl+β(1)L[C2min],Cl) were obtained, respectively. Using the values of the solution enthalpies and crystal energy of the ionic liquid, the dissociation enthalpy of [FeCl4]- anion, ΔHdis≈5659 kJ/mol, for the reaction: [FeCl4]-(g)→Fe3+(g)+4Cl-(g), was estimated. It is shown that the enthalpy of solution of the[C2mim][FeCl4] is small because the large hydration enthalpies of Fe3+, 4Cl- and [C2mim]- was compensated by the large dissociation enthalpy of [FeCl4]- anion, ΔdHm, in dissolution process of the IL.

Key words: Ionic liquid, Enthalpy of solution, Pitzer’s theory, Isoperibol calorimeter

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