Physical properties of polyacrylamide gels probed by AFM and rheology

被引:50
作者
Abidine, Yara [1 ,2 ]
Laurent, Valerie M. [1 ,2 ]
Michel, Richard [1 ,2 ]
Duperray, Alain [3 ,4 ]
Palade, Liviu Iulian [5 ]
Verdier, Claude [1 ,2 ]
机构
[1] Univ Grenoble Alpes, LIPHY, F-38000 Grenoble, France
[2] CNRS, LIPHY, F-38000 Grenoble, France
[3] INSERM, IAB, F-38000 Grenoble, France
[4] Univ Grenoble Alpes, IAB, F-38000 Grenoble, France
[5] Univ Lyon, CNRS, Inst Camille Jordan, UMR 5208,INSA Lyon,Pole Math, F-69621 Villeurbanne, France
关键词
ENTANGLED POLYMER-SOLUTIONS; DYNAMIC SHEAR; MICRORHEOLOGY; BEHAVIOR; POLYDIMETHYLSILOXANES; VISCOELASTICITY; RELAXATION; NETWORKS; MODULUS; MODEL;
D O I
10.1209/0295-5075/109/38003
中图分类号
O4 [物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Polymer gels have been shown to behave as viscoelastic materials but only a small amount of data is usually provided in the glass transition. In this paper, the dynamic moduli G ' and G '' of polyacrylamide hydrogels are investigated using both an AFM in contact force modulation mode and a classical rheometer. The validity is shown by the matching of the two techniques. Measurements are carried out on gels of increasing polymer concentration in a wide frequency range. A model based on fractional derivatives is successfully used, covering the whole frequency range. G(N)(0), the plateau modulus, as well as several other parameters are obtained at low frequencies. The model also predicts the slope a of both moduli in the glass transition, and a transition frequency f(T) is introduced to separate the gel-like behavior with the glassy state. Its variation with polymer content c gives a dependence fT similar to c(1.6), in good agreement with previous theories. Therefore, the AFM data provides new information on the physics of polymer gels. Copyright (C) EPLA, 2015
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页数:6
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