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室温离子液体 1-丁基-3-甲基咪唑六氟磷酸盐(bmimPF6)中,非离子表面活性剂的表面吸附和聚集形成。

Surface adsorption and aggregate formation of nonionic surfactants in a room temperature ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate (bmimPF6).

机构信息

Department of Pure and Applied Chemistry, Faculty of Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.

出版信息

J Colloid Interface Sci. 2011 Jun 15;358(2):527-33. doi: 10.1016/j.jcis.2011.03.055. Epub 2011 Mar 23.

Abstract

Surface adsorption and aggregation behavior of polyoxyethylene (POE)-type nonionic surfactants in a room temperature ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate (bmimPF(6)), were investigated by means of surface tension, (1)H NMR, and dynamic light-scattering (DLS) measurements. The maximum surface excess in bmimPF(6) is much lesser than those observed for aqueous solution, reflecting a much weaker solvophobicity exhibited by the surfactant hydrocarbon chain in the ionic liquid compared with the hydrophobicity experienced in water. Compared with another ionic liquid with different anion species, 1-butyl-3-methylimidazolium terafluoroborate (bmimBF(4)), the surfactant solution in bmimPF(6) brings about higher critical micelle concentration (cmc), smaller micellar aggregation number, and weaker dependence of cmc on the surfactant hydrocarbon chain length. This indicates that the solvophobic interaction between surfactant hydrocarbon chains acts more weakly in bmimPF(6) than in bmimBF(4). The weaker solvophobic effect in bmimPF(6) is also appreciable in the thermodynamic parameters for micelle formation derived from temperature dependence of cmc, and would be attributed to weaker attractive interaction between bmim cation and PF(6)(-) ion compared with that between bmim cation and BF(4)(-) ion. Present results give an insight into a better understanding of the importance of anion species for the properties of ionic liquids as a solvent to support a self-assembly of amphiphilic molecules.

摘要

通过表面张力、(1)H NMR 和动态光散射(DLS)测量,研究了聚氧乙烯(POE)型非离子表面活性剂在室温离子液体 1-丁基-3-甲基咪唑六氟磷酸盐(bmimPF6)中的表面吸附和聚集行为。在 bmimPF6 中,最大表面过剩量远小于在水溶液中观察到的表面过剩量,这反映了与在水中经历的疏水性相比,表面活性剂烃链在离子液体中表现出的疏溶剂化作用要弱得多。与具有不同阴离子种类的另一种离子液体 1-丁基-3-甲基咪唑四氟硼酸盐(bmimBF4)相比,bmimPF6 中的表面活性剂溶液具有更高的临界胶束浓度(cmc)、更小的胶束聚集数和对表面活性剂烃链长度依赖性更弱的 cmc。这表明,在 bmimPF6 中,表面活性剂烃链之间的疏溶剂相互作用比在 bmimBF4 中弱。在由 cmc 随温度的变化得出的胶束形成热力学参数中,也可以明显看出 bmimPF6 中较弱的疏溶剂效应,这归因于 bmim 阳离子与 PF6(-)离子之间的吸引力比 bmim 阳离子与 BF4(-)离子之间的吸引力弱。目前的结果为更好地理解阴离子种类对离子液体作为支持两亲分子自组装的溶剂的性质的重要性提供了深入了解。

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