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长链烷基离子液体的介观动力学与剪切松弛之间的关系。

Relationship between mesoscale dynamics and shear relaxation of ionic liquids with long alkyl chain.

机构信息

Department of Molecular Design and Engineering, Graduate School of Engineering, Furo-cho B2-3 (611), Chikusa, Nagoya, Aichi 464-8603, Japan.

出版信息

J Chem Phys. 2012 Sep 14;137(10):104511. doi: 10.1063/1.4751547.

Abstract

The shear relaxation spectra of three imidazolium-based ionic liquids, 1-methyl-3-octylimidazolium chloride ([C(8)mim][Cl]), 1-methyl-3-octylimidazolium hexafluorophosphate ([C(8)mim][PF(6)]), and 1-dodecyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ([C(12)mim][TFSA]) were measured and compared with the intermediate scattering functions determined with neutron spin echo (NSE) spectroscopy. The shear relaxation is slower than that predicted from the relaxation of the main peak of the structure factor that is common to other molecular liquids, whereas it is faster than that from the relaxation of the pre-peak, that corresponds to the correlation length of about 10 nm specific to ionic liquids with an intermediately long alkyl chain. The role of the pre-peak structure in the mechanism of shear viscosity of ionic liquids is discussed based on the comparison between NSE and shear relaxations.

摘要

三种咪唑基离子液体(1-甲基-3-辛基咪唑氯化物([C(8)mim][Cl])、1-甲基-3-辛基咪唑六氟磷酸盐([C(8)mim][PF(6)])和 1-十二烷基-3-甲基咪唑双(三氟甲烷磺酰基)酰胺([C(12)mim][TFSA])的剪切松弛谱进行了测量,并与中子自旋回波(NSE)光谱确定的中间散射函数进行了比较。剪切松弛比其他分子液体中常见的结构因子主峰松弛预测的要慢,而比对应于约 10nm 的相关长度的前峰松弛要快,前峰松弛对应于具有中等长度烷基链的离子液体的特征。基于 NSE 和剪切松弛之间的比较,讨论了前峰结构在离子液体剪切粘度机制中的作用。

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