Department of Materials Science and Technology, Nagaoka University of Technology, Kamitomioka 1603-1, Nagaoka 940-2188, Japan.
Department of Materials Science and Technology, Nagaoka University of Technology, Kamitomioka 1603-1, Nagaoka 940-2188, Japan.
Ultrason Sonochem. 2016 Jan;28:39-46. doi: 10.1016/j.ultsonch.2015.06.030. Epub 2015 Jun 30.
Ultrasound (US) effect on 1-butyl-3-methyl-imidazolium (BMI) ionic liquids having different counter anions, BF4(-), PF6(-) and Cl(-) in aqueous medium was studied by FT-IR spectroscopy. Their deconvolution spectra were used to analyze the change of hydrogen bond in the absence and presence of US exposure to the ionic liquid. The FT-IR spectra were measured in different water contents without and with US at 23 kHz. These results indicated that the counter anion species in the imidazole based the ionic liquids played an important role for water solvation, when the US was exposed. The US hardly changed hydrogen bonding in the aqueous BMI-PF6, while the BMI-BF4 and BMI-Cl showed obvious change in their FT-IR spectra. Especially for the BMI-Cl, significant change was observed by the US exposure in the range of 2.6 wt% to 20 wt% of water contents. The results showed that the US could break the hydrogen bond in the BMI-Cl ionic liquids. In the case of BMI-BF4, the FT-IR band at 950-1152 cm(-1) was significantly intensified under US exposure, due to that the US influenced BF4(-)-water interaction. But, it was observed that the ionic liquid having PF6(-) was very less changed in the US system.
在水介质中,通过傅里叶变换红外光谱法(FT-IR)研究了不同抗衡阴离子 BF4(-)、PF6(-)和 Cl(-)的 1-丁基-3-甲基咪唑(BMI)离子液体在超声(US)作用下的影响。使用无 US 和有 US 暴露于离子液体时的解卷积光谱来分析氢键的变化。在不同含水量下测量了 FT-IR 光谱,没有和有 US 分别在 23 kHz 下进行。这些结果表明,当 US 暴露时,离子液体中咪唑基的抗衡阴离子种类对水的溶解起着重要作用。US 几乎没有改变水合 BMI-PF6 中的氢键,而 BMI-BF4 和 BMI-Cl 在其 FT-IR 光谱中显示出明显的变化。特别是对于 BMI-Cl,在 2.6 wt%至 20 wt%含水量范围内,通过 US 暴露观察到明显的变化。结果表明,US 可以破坏 BMI-Cl 离子液体中的氢键。在 BMI-BF4 的情况下,由于 US 影响 BF4(-)-水相互作用,在 US 暴露下,950-1152 cm(-1)处的 FT-IR 带显著增强。但是,观察到 PF6(-)的离子液体在 US 体系中变化很小。