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Local Dynamics of Micelles of New Long-Chain Surfactants in Aqueous Media

机译:新型长链表面活性剂在水介质中胶束的局部动力学

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The molecular dynamics, organization, and phase state of aqueous solutions of new long-chain cationic surfactants with saturated hydrocarbon radicals (from C-16 to C-22) containing one or two hydroxyl groups in their polar heads are studied by the spin-probe EPR spectroscopy. In the region of micellar solutions, local mobility of surfactant molecules slightly changes with an increase in the length of hydrocarbon radical, whereas the order parameter of micelles increases notably. The addition of two hydroxyl groups to the polar part of long-chain (C-22) surfactant molecule considerably decreases local mobility and increases the ordering of micellar system compared to the micelles of analogous surfactant with one hydroxyl group. Phase transition from micellar to a solid state is observed in this system with a decrease in temperature. The addition of KCl to aqueous surfactant solution lowers the local mobility, increases the order parameter of micelles, and can cause changes in the phase state of a system. In the presence of salt, the correlation time of probe rotation and its order parameter depend on surfactant concentration. Apparently, this is explained by changes in the shape of micelles upon variations in surfactant concentration.
机译:通过自旋探针研究了新型长链阳离子表面活性剂水溶液的分子动力学,组织和相态,这些表面活性剂的极性头具有一个或两个羟基的饱和烃基(从C-16到C-22)。 EPR光谱。在胶束溶液的区域中,表面活性剂分子的局部迁移率随烃基长度的增加而略有变化,而胶束的有序参数则显着增加。与具有一个羟基的类似表面活性剂的胶束相比,向长链(C-22)表面活性剂分子的极性部分添加两个羟基可显着降低局部迁移率并增加胶束体系的有序性。在该系统中观察到从胶束到固态的相变,并且温度降低。向表面活性剂水溶液中添加KCl会降低局部迁移率,增加胶束的有序参数,并可能导致系统相态的变化。在盐的存在下,探针旋转的相关时间及其有序参数取决于表面活性剂的浓度。显然,这可以通过表面活性剂浓度变化时胶束形状的变化来解释。

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