Synthesis of trisiloxane-tailed surface active ionic liquids and their aggregation behavior in aqueous solution

被引:37
作者
Du, Zhiping [1 ,2 ]
Li, Enze [1 ]
Cao, Yang [1 ]
Li, Xiang [1 ]
Wang, Guoyong [1 ]
机构
[1] China Res Inst Daily Chem Ind, Taiyuan 030001, Shanxi, Peoples R China
[2] Shanxi Univ, Inst Resources & Environm Engn, Taiyuan 030006, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Ionic liquids; Aggregation behavior; Trisiloxane-tailed; Surface active; Vesicular-like; MICELLE FORMATION; ADSORPTION;
D O I
10.1016/j.colsurfa.2013.10.004
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
The aggregation behavior of two trisiloxane-tailed surface active ionic liquids (ILs), 1-methyl-3-trisilox-aneimidazolium chloride ([Si(3)Mim]CI) and trisiloxanepyridinium chloride ([Si(3)Py]CI), in aqueous solution was investigated by the measurement of surface tension, electrical conductivity, transmission electron microscopy (TEM), dynamic light scattering (DLS), and X-ray diffraction (XRD). The surface tension measurement showed the critical aggregation concentration (cac) of [Si(3)Mim]CI and [Si(3)Py]Cl is 15.5 and 24.8 mmoll(-1) respectively, and the corresponding surface tension at cac (gamma(cac)) is 23.8 and 23.0 mN m(-1), respectively. The phenomenon was mainly ascribed to the branched trisiloxane hydrophobic moieties and these results demonstrated that the surface activity of these trisiloxane-tailed ILs was somewhat superior to that of conventional ILs. The vesicular-like structure of the aggregates was observed by TEM while DLS provided the diameter distribution of these aggregates. In addition, a probable two-layered arrangement of molecules in aggregates for the two ILs in aqueous solution was proposed based upon the results of XRD studies. This investigation may contribute to expand understanding of trisiloxane-tailed ILs. Furthermore, high thermal stability of such compounds may improve their potential applications in the fields of colloids and interfaces science. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:744 / 751
页数:8
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