Physicochemical properties of 1,3-dialkylimidazolium fluorohydrogenate room-temperature molten salts

被引:130
作者
Hagiwara, R [1 ]
Matsumoto, K
Nakamori, Y
Tsuda, T
Ito, Y
Matsumoto, H
Momota, K
机构
[1] Kyoto Univ, Grad Sch Energy Sci, Sakyo Ku, Kyoto 6068501, Japan
[2] Natl Inst Adv Ind Sci & Technol, Osaka 5638577, Japan
[3] Morita Chem Ind Co Ltd, Yodogawa Ku, Osaka 5320002, Japan
关键词
D O I
10.1149/1.1621414
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Reaction of some N-alkylimidazolium chlorides with anhydrous hydrogen fluoride (HF) gave nonvolatile room temperature molten salts (room temperature ionic liquids), RMImF.2.3HF where RMIm = 1,3-dimethylimidazolium (DMIm), 1-ethyl-3-methylimidazolium (EMIm), 1-methyl-3-propylimidazolium, 1-butyl-3-methylimidazolium, 1-methyl-3-pentylimidazolium, and 1-hexyl-3-methylimidazolium. Vacuum stable salts at room temperature exhibited similar stoichiometry regardless of the type of cation. In the differential scanning calorimetry (DSC) curve, DMImF.2.3HF exhibited both the freezing and melting on the cooling and heating process, respectively, while EMImF.2.3HF showed the glass transition on the cooling process and devitrification and melting on the heating process. The other salts show only the glass transition on the DSC curves. High specific conductivities, 110 and 100 mS cm(-1), were observed at 298 K for DMImF.2.3HF and EMImF.2.3HF, respectively. Introduction of the longer alkyl side chains to the imidazolium cation increased the viscosity and decreased the conductivity. These salts were stable in air and did not etch a Pyrex glass container at ambient conditions. The dissociation pressures of HF from the salts were negligibly small at ambient condition. The electrochemical windows of these salts was about 3 V. (C) 2003 The Electrochemical Society.
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页码:D195 / D199
页数:5
相关论文
共 27 条
[1]  
AZMAN A, 1967, CAN J CHEMISTRY, V45, P1347
[2]   NMR SPECTRUM OF A NEARLY LINEAR 5-SPIN SYSTEM - HYDROGEN BONDING IN KH2F3 [J].
BLINC, R ;
TRONTELJ, Z ;
VOLAVSEK, B .
JOURNAL OF CHEMICAL PHYSICS, 1966, 44 (03) :1028-&
[3]   Hydrophobic, highly conductive ambient-temperature molten salts [J].
Bonhote, P ;
Dias, AP ;
Papageorgiou, N ;
Kalyanasundaram, K ;
Gratzel, M .
INORGANIC CHEMISTRY, 1996, 35 (05) :1168-1178
[4]   STUDY OF LOW-FREQUENCY MOLECULAR MOTIONS IN HF, KHF2, KH2F3, AND NAH2F3 [J].
BOUTIN, H ;
BRAJOVIC, V ;
SAFFORD, GJ .
JOURNAL OF CHEMICAL PHYSICS, 1963, 39 (11) :3135-&
[5]   Freezing points and vapor pressures of the system potassium fluoride-hydrogen fluoride [J].
Cady, GH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1934, 56 (07) :1431-1434
[6]   CRYSTAL STRUCTURE OF KH2F3 AND GEOMETRY OF H2F-/3 ION [J].
FORRESTER, JD ;
TEMPLETON, DH ;
ZALKIN, A ;
SENKO, ME .
ACTA CRYSTALLOGRAPHICA, 1963, 16 (01) :58-&
[7]   RECOMMENDATIONS ON REPORTING ELECTRODE-POTENTIALS IN NONAQUEOUS SOLVENTS (RECOMMENDATIONS 1983) [J].
GRITZNER, G ;
KUTA, J .
PURE AND APPLIED CHEMISTRY, 1984, 56 (04) :461-466
[8]   Acidic 1-ethyl-3-methylimidazolium fluoride: a new room temperature ionic liquid [J].
Hagiwara, R ;
Hirashige, T ;
Tsuda, T ;
Ito, Y .
JOURNAL OF FLUORINE CHEMISTRY, 1999, 99 (01) :1-3
[9]  
Hagiwara R, 2001, PROCEEDINGS OF THE 6TH INTERNATIONAL SYMPOSIUM ON MOLTEN SALT CHEMISTRY AND TECHNOLOGY, P136
[10]   A highly conductive room temperature molten fluoride:: EMIF•2.3HF [J].
Hagiwara, R ;
Hirashige, T ;
Tsuda, T ;
Ito, Y .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (01) :D1-D6