化学
微乳液
肺表面活性物质
辛醇
碘化物
无机化学
水溶液
吸附
氯化锂
盐析
双水相体系
钠
乙醇
十二烷基苯磺酸钠
锂(药物)
相(物质)
表面张力
滴定法
盐(化学)
有机化学
分配系数
医学
生物化学
物理
量子力学
内分泌学
作者
Sebastian Schöttl,Dominik Horinek
摘要
The weakly associated micellar aggregates found in the so-called “pre-ouzo region” of the surfactant-free microemulsion water/ethanol/1-octanol are sensitive to changes in the system composition and also to the presence of additives like salt. In this work, we study the influence of two salts, sodium iodide and lithium chloride, on aggregates in water/ethanol/1-octanol by molecular dynamics simulations. In both cases, ethanol concentration in the nonpolar phase and at the interface is increased due to a salting out effect on ethanol in the aqueous pseudo-phase. In addition, minor charging of the interface as a consequence of differential adsorption of anions and cations occurs. However, this charge separation is overall weakened by the erratic surface of octanol aggregates, where polar hydroxyl groups and hydrophobic patches are both present. Furthermore, ethanol at the interface shields hydrophobic patches and reduces the preferential adsorption of iodide and lithium.
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