PROBING POLYMER SURFACE AND INTERFACE DYNAMICS

被引:24
作者
ANDRADE, JD [1 ]
CHEN, WY [1 ]
机构
[1] UNIV UTAH,DEPT MAT SCI,SALT LAKE CITY,UT 84112
关键词
SURFACES - Spectroscopic Analysis;
D O I
10.1002/sia.740080606
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
Polymer molecules and segments at surfaces and interfaces also exhibit motions and relaxations. In air or vacuum, such motions 'permit' the surface to restructure to minimize the surface free energy. In aqueous solution, the polymer surface restructures and reorients to optimally interact with the aqueous solvent, thereby minimizing the interfacial free energy. XPS and related high vacuum techniques probe the vacuum-equilibrated surface. The best way to probe the polymer-liquid interface is via dynamic contact angle or wetting methods. A number of issues and concerns are discussed: (1) the size of hierarchy of structures; (2) the time course of surface dynamic processes; (3) theory, modeling, and simulation of surface dynamics; and (4) experimental methods.
引用
收藏
页码:253 / 256
页数:4
相关论文
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