Quantifying the elasticity and viscosity of geometrically confined polymer films via thermal wrinkling

被引:14
作者
Chan, Edwin P. [1 ]
Lin, Qinghuang [2 ]
Stafford, Christopher M. [1 ]
机构
[1] NIST, Div Polymers, Gaithersburg, MD 20899 USA
[2] IBM TJ Watson Res Ctr, Yorktown Hts, NY 10598 USA
关键词
mechanical properties; networks; relaxation; stress; stress relaxation; surface wrinkling; thin films; viscoelastic properties;
D O I
10.1002/polb.23152
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We apply thermal wrinkling, which is a surface instability that occurs during thermal annealing of polymer films geometrically confined by a rigid substrate and a flexible superstrate, to study the elasticity and viscosity of chemically crosslinked polymer systems. Specifically, we study the thermal wrinkling of aluminum-capped polyhydroxystyrene films with different extent of chemical crosslinking and find that that the rate of change of the wrinkling wavelength with annealing time and temperature has unique relationships with the elasticity and viscosity of the polymer network. With the aid of analytical expressions that relate the time- and temperature-dependent evolution of the wrinkle wavelength to the elasticity and viscosity, we are able to quantify the elastic modulus and shear viscosity of geometrically confined polymer thin films as a function of the degree of crosslinking. (C) 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2012
引用
收藏
页码:1556 / 1561
页数:6
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