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Tilting phase transition of amphiphile monolayers at the air-water interface: Physically reasoning phase portion in a phase diagram

机译:两亲性单分子层在空气-水界面处的倾斜相变:相图中的物理推理相部分

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摘要

The untilting to tilting (U-->t) phase transition of amphiphile monolayers at the water-air interface is studied as a distortion of the orthogonally hexagonal orientation of molecules by a competition among entropy, Lennard-Jones potential, and the work done by surface and bulk pressures (Pi,P). The U/t phase portion in the Pi-T diagram is derived as an approximately linear van der Waals equation Pi=kT/2A(0)-Pl(0) with A(0), l(0) being the molecular area and chain length, respectively, at the U phase. A comparison with experiment in monolayers of C-14-C-24 acids [see, e.g., Peterson , Langmuir 8, 2995 (1992)] shows quantitative agreement. Besides two optimal tilting directions, i.e., in the direction to a nearest neighbor (NN) and to a next-nearest neighbor (NNN), an intermediate tilt at the NN-->NNN transition is shown to be physically possible based on Selinger-Nelson theory [Phys. Rev. Lett. 61, 416 (1988)]. (C) 2002 American Institute of Physics. [References: 41]
机译:通过熵,伦纳德·琼斯势能之间的竞争,研究了两亲性单分子层在水-空气界面的直至倾斜(U→t)的相变,作为分子正交六边形取向的扭曲。表面和体积压力(Pi,P)。 Pi-T图中的U / t相部分为近似线性范德华方程式Pi = kT / 2A(0)-Pl(0),其中A(0),l(0)是分子面积, U阶段的链长。与C-14-C-24酸单层中的实验的比较[参见,例如,Peterson,Langmuir 8,2995(1992)]显示出定量的一致性。除了两个最佳倾斜方向(即朝最近的邻居(NN)和最近的下一个邻居(NNN)的方向)外,根据Selinger-尼尔森理论[Phys。牧师61,416(1988)]。 (C)2002美国物理研究所。 [参考:41]

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