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热响应性表面薄膜相变的范德瓦尔斯模型

Van der Waals model for phase transitions in thermoresponsive surface films.

作者信息

McCoy John D, Curro John G

机构信息

Department of Materials and Metallurgical Engineering, New Mexico Institute of Mining and Technology, Socorro, New Mexico 87801, USA.

出版信息

J Chem Phys. 2009 May 21;130(19):194708. doi: 10.1063/1.3138905.

Abstract

Phase transitions in polymeric surface films are studied with a simple model based on the van der Waals equation of state. Each chain is modeled by a single bead attached to the surface by an entropic-Hooke's law spring. The surface coverage is controlled by adjusting the chemical potential, and the equilibrium density profile is calculated with density functional theory. The interesting feature of this model is the multivalued nature of the density profile seen at low temperature. This van der Waals loop behavior is resolved with a Maxwell construction between a high-density phase near the wall and a low-density phase in a "vertical" phase transition. Signatures of the phase transition in experimentally measurable quantities are then found. Numerical calculations are presented for isotherms of surface pressure, for the Poisson ratio, and for the swelling ratio.

摘要

利用基于范德瓦尔斯状态方程的简单模型研究了聚合物表面膜中的相变。每条链由一个通过熵胡克定律弹簧附着在表面的单个珠子来建模。通过调节化学势来控制表面覆盖率,并利用密度泛函理论计算平衡密度分布。该模型的有趣特征是在低温下看到的密度分布的多值性质。这种范德瓦尔斯回路行为通过在壁附近的高密度相和“垂直”相变中的低密度相之间的麦克斯韦构造得到解决。然后找到了实验可测量量中相变的特征。给出了表面压力等温线、泊松比和溶胀比的数值计算结果。

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