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Surfactant properties and their influence on micellar solubilization of hydrocarbons.

机译:表面活性剂性质及其对烃胶束增溶的影响。

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To better understand the solubilization properties of surfactant for different classes of hydrocarbons, the critical micelle concentration must be obtained for each surfactant against certain hydrocarbon and this information can be measured from interfacial tension tests. The area per surfactant molecule on the interface can also be obtained from interfacial tension. Aggregation numbers for each system can be obtained by pyrene fluorescence quenching experiments, combining the micellar solubilization rate which is measured by G.C measurements, the composition of one micelle can be clearly clarified.; The dodecane/dodecylbenenesulfonate (DBS) and benzene/(DBS) micelles are examined here to explore the differences in the micelle structure and solubilization of dodecane and benzene in DBS micelles. The coordinate of each atom for a micellar system is rendered in a spherical control volume with their hydrophilic group facing water molecules that surround the micelle and hydrophobic tail stays within the interior of the micelle, the amount of molecules that form one micelle is based on the experimental results, energy minimization is performed to remove bad contacts within molecules. Molecular dynamic simulation with the CHARMM force field is conducted at constant NPT for one nano second and no additional constraint during the simulation. The equilibrated system results in a micelle structure in which water molecules do not penetrate into the interior of the micelle. Dodecane molecules stay in the core of the micelle due the movement of dodecane molecules are highly confined and hindered by the tail of the surfactant while the benzene molecules position themselves evenly among the whole micelle without any restriction. The radial distribution functions extracted from the output of the simulation show a highly ordered structure is preferred for a stable micelle. Experimental and Simulation details, micelle structures, and the atomic radial, probability and density functions will be presented.
机译:为了更好地理解表面活性剂对不同种类的烃的增溶性能,必须获得每种表面活性剂对某些烃的临界胶束浓度,并且可以通过界面张力测试测量该信息。界面张力上每个表面活性剂分子的面积也可以从界面张力获得。可以通过pyr荧光猝灭实验获得每个系统的聚集数,结合通过G.C测量测得的胶束增溶速率,可以清楚地阐明一个胶束的组成。在这里检查十二烷/十二烷基苯磺酸盐(DBS)和苯/(DBS)胶束,以探索十二烷和苯在DBS胶束中的胶束结构和增溶作用的差异。胶束系统中每个原子的坐标以球形控制体积表示,其亲水基团面对着围绕在胶束中的水分子,而疏水尾巴则停留在胶束内部,形成一个胶束的分子数量基于实验结果表明,进行了能量最小化以去除分子内的不良接触。使用CHARMM力场的分子动力学模拟在恒定NPT下进行一纳秒,并且在模拟过程中没有其他约束。平衡的系统导致胶束结构,其中水分子不渗透到胶束内部。十二烷分子停留在胶束的核心,因为十二烷分子的移动受到表面活性剂尾部的高度限制和阻碍,而苯分子则在整个胶束中均匀地定位,没有任何限制。从模拟输出中提取的径向分布函数表明,对于稳定的胶束而言,高度有序的结构是首选。将介绍实验和仿真的详细信息,胶束结构以及原子径向,概率和密度函数。

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