Department of Molecular Design and Engineering, Graduate School of Engineering, Nagoya University, Furo-cho B2-3(611), Chikusa, Nagoya, Aichi 464-8603, Japan.
J Phys Chem B. 2010 Jun 24;114(24):8126-33. doi: 10.1021/jp1024137.
The frequency-dependent shear viscosities of four representative imidazolium-based room-temperature ionic liquids, 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ([bmim][TFSA]), 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim][PF(6)]), 1-hexyl-3-methylimidazolium hexafluorophosphate ([hmim][PF(6)]), and 1-methyl-3-octylimidazolium hexafluorophosphate ([omim][PF(6)]), are measured from 5 to 205 MHz with shear impedance spectroscopy. A relaxation is observed in the measured frequency range in all cases. This is the first report on the shear relaxation of ionic liquids at room temperature, to our best knowledge. Comparing the spectra of the common cations, [bmim][TFSA] and [bmim][PF(6)], the normalized relaxation spectra, eta(nu)/eta(0), reduce to a single curve when plotted against eta(0)nu, where nu and eta(0) stand for the frequency and shear viscosity, respectively. The lower viscosity of the TFSA salt is thus elucidated by the shorter relaxation time. The lower viscosity at higher temperature is also attributed to the shorter relaxation time. On the other hand, the increase in the length of the alkyl chain of the cation leads to the lower-frequency shift of the relaxation frequency on the eta(0)nu scale. Therefore, the higher viscosity of the omim salt is the result of the compensation of the longer relaxation time for the smaller high-frequency shear modulus. In addition, the relaxation time distribution becomes broader with increasing chain length, which can be ascribed to the heterogeneity of the liquid structure.
四种典型的咪唑基室温离子液体,1-丁基-3-甲基咪唑双(三氟甲烷磺酰基)酰胺([bmim][TFSA])、1-丁基-3-甲基咪唑六氟磷酸盐([bmim][PF(6)])、1-己基-3-甲基咪唑六氟磷酸盐([hmim][PF(6)])和 1-甲基-3-辛基咪唑六氟磷酸盐([omim][PF(6)])的剪切粘度随频率变化的测量结果在 5 到 205MHz 之间采用剪切阻抗谱法得到。在所有情况下,在测量的频率范围内都观察到弛豫现象。据我们所知,这是室温下离子液体剪切弛豫的首次报道。将常见阳离子[bmim][TFSA]和[bmim][PF(6)]的谱进行比较,当以η(0)ν为横坐标,η(nu)/η(0)为纵坐标作图时,归一化的弛豫谱可以简化为一条曲线,其中 ν 和 η(0)分别表示频率和剪切粘度。因此,TFSA 盐的粘度较低是由于弛豫时间较短。在较高温度下粘度较低也是由于弛豫时间较短。另一方面,阳离子烷基链的长度增加导致弛豫频率在η(0)ν标度上的低频移动。因此,omim 盐的较高粘度是较长弛豫时间对较小高频剪切模量的补偿结果。此外,随着链长的增加,弛豫时间分布变得更宽,这可以归因于液体结构的不均匀性。