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电解质对 1-丁基-3-甲基咪唑十二烷基硫酸盐在水溶液中聚集行为的影响。

Electrolyte effect on the aggregation behavior of 1-butyl-3-methylimidazolium dodecylsulfate in aqueous solution.

机构信息

Key Laboratory of Colloid and Interface Chemistry, Shandong University, Ministry of Education, Jinan 250100, PR China.

出版信息

J Colloid Interface Sci. 2013 Jul 15;402:139-45. doi: 10.1016/j.jcis.2013.03.027. Epub 2013 Apr 10.

DOI:10.1016/j.jcis.2013.03.027
PMID:23642809
Abstract

Effect of three inorganic electrolytes (LiCl, NaCl, and MgCl2) and four organic electrolytes, viz. tetraalkylammonium bromides ((CH3)4NBr, (C2H5)4NBr, (C3H7)4NBr, and (C4H9)4NBr) on the aggregation behavior of the anionic halogen-free surface active ionic liquid, 1-butyl-3-methylimidazolium dodecylsulfate ([C4mim][C12SO4]), in aqueous solution was studied by surface tension, steady-state fluorescence quenching, and dynamic light scattering measurements. The results show that all the electrolytes investigated have a salting-out effect, which promotes aggregate formation of [C4mim][C12SO4]. The stronger hydrophobicity of organic electrolytes is crucial for the superior influence on the surface activity of [C4mim][C12SO4]. However, the stabilization energy results obtained by quantum chemical calculations prove that although the promoting effect of organic cations (tetraalkylammonium cations) on the micellization process of [C4mim][C12SO4] is powerful, they mainly act as counterions. For a given electrolyte (i.e., NaCl), critical micelle concentration of [C4mim][C12SO4] decreases with increasing electrolyte concentration. The average aggregation number and aggregate size of [C4mim][C12SO4] were shown to change slightly in the presence of various electrolytes, except for MgCl2. Anyway, hydrophobicity together with bulkiness and hydration ability of cations of the added electrolytes are suggested to play important roles in modifying the aggregation behavior of [C4mim][C12SO4] in aqueous solution.

摘要

三种无机电解质(LiCl、NaCl 和 MgCl2)和四种有机电解质,即四烷基溴化铵((CH3)4NBr、(C2H5)4NBr、(C3H7)4NBr 和(C4H9)4NBr)对阴离子无卤表面活性剂 1-丁基-3-甲基咪唑硫酸十二烷基酯([C4mim][C12SO4])在水溶液中的聚集行为的影响通过表面张力、稳态荧光猝灭和动态光散射测量进行了研究。结果表明,所有研究的电解质都具有盐析效应,促进了[C4mim][C12SO4]的聚集形成。有机电解质较强的疏水性对[C4mim][C12SO4]的表面活性具有重要影响。然而,通过量子化学计算得到的稳定能结果证明,尽管有机阳离子(四烷基铵阳离子)对[C4mim][C12SO4]的胶束化过程具有促进作用,但它们主要起抗衡离子的作用。对于给定的电解质(即 NaCl),[C4mim][C12SO4]的临界胶束浓度随着电解质浓度的增加而降低。在各种电解质存在下,[C4mim][C12SO4]的平均聚集数和聚集尺寸变化不大,除了 MgCl2。总之,添加电解质的阳离子的疏水性以及其体积和水化能力被认为在修饰[C4mim][C12SO4]在水溶液中的聚集行为方面起着重要作用。

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