Viscoelastic dewetting of constrained polymer thin films

被引:43
|
作者
Gabriele, Sylvain
Damman, Pascal
Sclavons, Severine
Desprez, Sylvain
Coppee, Severine
Reiter, Guenter
Hamieh, Moustafa
Al Akhrass, Samer
Vilmin, Thomas
Raphael, Elie
机构
[1] Univ Mons, Lab Physicochim Polymeres, B-7000 Mons, Belgium
[2] Ctr Natl Rech Sci UPR9069, Unite Propre Rech, Inst Chim Surface & Interfaces, F-68057 Mulhouse, France
[3] Univ Libanaise, Fac Sci 1, Dept Chim, Lab Chim Analyt Mat Surface & Interfaces, Hadeth, Beyrouth, Libya
[4] Ecole Super Phys & Chim Ind Ville Paris, Lab Physicochim Theorique, Unite Mixte Rech, Ctr Natl Rech Sci 7083, F-75231 Paris 05, France
关键词
dewetting instability; interfaces; polystyrene; thin films; viscoelasticity;
D O I
10.1002/polb.20919
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Thin films of fluids are playing a leading role in countless natural and industrial processes. Here we study the stability and dewetting dynamics of viscoelastic polymer thin films. The dewetting of polystyrene close to the glass transition reveals unexpected features: asymmetric rims collecting the dewetted liquid and logarithmic growth laws that we explain by considering the nonlinear velocity dependence of friction at the fluid/solid interface and by evoking residual stresses within the film. Systematically varying the time so that films were stored below the glass-transition temperature, we studied simultaneously the probability for film rupture and the dewetting dynamics at early stages. Both approaches proved independently the significance of residual stresses arising from the fast solvent evaporation associated with the spin-coating process. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:3022 / 3030
页数:9
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