Glass Transition Accelerates the Spreading of Polar Solvents on a Soluble Polymer

被引:27
作者
Dupas, Julien [1 ]
Verneuil, Emilie [1 ]
Van Landeghem, Maxime [1 ]
Bresson, Bruno [1 ]
Forny, Laurent [2 ]
Ramaioli, Marco [2 ]
Lequeux, Francois [1 ]
Talini, Laurence [1 ]
机构
[1] CNRS UPMC ESPCI ParisTech PSL Res Univ, Lab SIMM, UMR 7615, F-75231 Paris, France
[2] Nestle Res Ctr, CH-1000 Lausanne 26, Switzerland
关键词
THIN; DYNAMICS; BEHAVIOR; FILMS; FIELD;
D O I
10.1103/PhysRevLett.112.188302
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
We study the wetting of polymer layers by polar solvents. As previously observed, when a droplet of solvent spreads, both its contact angle and velocity decrease with time as a result of solvent transfers from the droplet to the substrate. We show that, when the polymer is initially glassy, the angle decreases steeply for a given value of the velocity, U-g. We demonstrate that those variations result from a plasticization, i.e., a glass transition, undergone by the polymer layer during spreading, owing to the increase of its solvent content. By analyzing previous predictions on the wetting of rigid and soft viscoelastic substrates, we relate U-g to the viscosity of the polymer gel close to the glass transition. Finally, we derive an analytical prediction for U-g based on existing predictions for the water transfer from the droplet to the substrate. Using polar solvents of different natures, we show that the experimental data compare well to the predicted expression for U-g.
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页数:5
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