Association of methanol and water in ionic liquids elucidated by infrared spectroscopy using two-dimensional correlation and multivariate curve resolution

被引:132
|
作者
Lopez-Pastor, Mercedes
Ayora-Canada, Maria Jose
Valcarcel, Miguel
Lendl, Bernhard
机构
[1] Vienna Univ Technol, Inst Chem Technol & Analyt, A-1060 Vienna, Austria
[2] Univ Jaen, Dept Phys & Analyt Chem, E-23071 Jaen, Spain
[3] Univ Cordoba, Dept Analyt Chem, E-14071 Cordoba, Spain
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2006年 / 110卷 / 22期
关键词
D O I
10.1021/jp057398b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Water and methanol associations in ionic liquids (ILs) have been studied by means of FTIR spectroscopy. Spectra at different concentrations of water or methanol in ILs were obtained by means of on-line dilution using a flow injection analysis system. Spectral features in the OH stretching region revealed that most of the water and methanol molecules tended to be isolated from each other and to interact with the anion of the IL via H bonding. By means of two-dimensional correlation spectroscopy, the formation of methanol and water dimers was also detected. Multivariate curve resolution was used to recover pure spectra and concentration profiles of the different species. Methanol dimers form at concentrations higher than 0.8% (w/w) in the three studied ILs, 1-ethyl-3-methylimidazolium tetrafluoroborate (emimBF(4)), 1-butyl-3-methylimidazolium tetrafluoroborate (bmimBF(4)), and 1-butyl-3-methylimidazolium hexafluorophosphate (bmimPF(6)). Self-association of water molecules takes place in emimBF(4) and bmimBF(4) at a molar ratio similar to that of methanol molecules; however, water dimers cannot be detected in bmimPF(6), the most hydrophobic IL studied. No evidence was found that bigger water clusters are formed in these ILs at the studied cosolvent concentrations.
引用
收藏
页码:10896 / 10902
页数:7
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