Van der Waals model for phase transitions in thermoresponsive surface films

被引:4
|
作者
McCoy, John D. [1 ]
Curro, John G. [2 ]
机构
[1] New Mexico Inst Min & Technol, Dept Mat & Met Engn, Socorro, NM 87801 USA
[2] Univ New Mexico, Dept Chem & Nucl Engn, Albuquerque, NM 87185 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2009年 / 130卷 / 19期
关键词
chemical potential; density functional theory; equations of state; Poisson ratio; polymer films; surface phase transformations; swelling; van der Waals forces; DENSITY-FUNCTIONAL THEORY; LONG-CHAIN MOLECULES; AIR-WATER-INTERFACE; TETHERED POLYMER-CHAINS; LIPID BILAYER-MEMBRANES; CONSISTENT-FIELD THEORY; MONTE-CARLO-SIMULATION; EQUATION-OF-STATE; LANGMUIR MONOLAYERS; STATISTICAL THERMODYNAMICS;
D O I
10.1063/1.3138905
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
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页数:9
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