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NaBr induced strong adsorption of bis-(quaternary ammonium) gemini surfactants with long polymethylene spacer chain at air/water interface

机译:NaBr诱导在空气/水界面具有长聚亚甲基间隔链的双-(季铵)双子表面活性剂的强吸附

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摘要

The adsorption of alkanediyl-α,ω-bis(dimethyldodecylammonium bromide) (referred to as 12-s-12, s=12, 14 and 16) at the air/water interface in the absence and the presence of 10mmolL~(-1) NaBr has been investigated using surface tension measurements. The addition of salt strongly promoted the adsorption of 12-s-12, resulting in the formation of the double layers in the subphase below the main adsorption layer. In the double layers, the alkyl tails of surfactants were wrapped in the two layers of the heads and the long and flexible spacer chains were bent to insert into the alkyl tails. The π-A isotherm and surface dilational elasticity measurements supported this hypothesis. The reason may be due to the high hydrophobicity of the 12-s-12 with a long and flexible spacer chain. With addition of salt, the polarity of the solution environment was increased, which expelled the 12-s-12 from the bulk solution. The 12-s-12 molecules concentrated in the domain close to the interface formed the core-shell structure in order that the hydrocarbon chains could escape from the contact with water.
机译:在不存在和存在10mmolL〜(-1)的情况下,空气/水界面处烷二基-α,ω-双(二甲基十二烷基溴化铵)的吸附(称为12-s-12,s = 12、14和16) )已使用表面张力测量研究了NaBr。盐的加入强烈促进了12-s-12的吸附,导致在主吸附层下方的子相中形成双层。在双层中,表面活性剂的烷基尾部包裹在头部的两层中,弯曲的长而柔性的间隔链弯曲以插入到烷基尾部中。 π-A等温线和表面膨胀弹性测量结果支持了这一假设。原因可能是由于12-s-12具有长而灵活的间隔链的高疏水性。加入盐后,溶液环境的极性增加,从而使12-s-12从本体溶液中排出。集中在靠近界面的区域中的12-s-12分子形成核-壳结构,以便烃链可以从与水的接触中逸出。

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