Rossi Marco, Nardinocchi Paola, Wallmersperger Thomas
Institute of Solid Mechanics, TU Dresden, George-Bähr-Straße 3c, Dresden 01069, Germany.
Dresden Center for Computational Materials Science (DCMS), TU Dresden, Hallwachsstraße 3, Dresden 01069, Germany.
Proc Math Phys Eng Sci. 2019 Oct;475(2230):20190174. doi: 10.1098/rspa.2019.0174. Epub 2019 Oct 9.
Polymer gels are porous fluid-saturated materials which can swell or shrink triggered by various stimuli. The swelling/shrinking-induced deformation can generate large stresses which may lead to the failure of the material. In the present research, a nonlinear stress-diffusion model is employed to investigate the stress and the deformation state arising in hydrated constrained polymer gels when subject to a varying chemical potential. Two different constraint configurations are taken into account: (i) elastic constraint along the thickness direction and (ii) plane elastic constraint. The first step entirely defines a compressed/tensed configuration. From there, an incremental chemo-mechanical analysis is presented. The derived model extends the classical linear poroelastic theory with respect to a prestressed configuration. Finally, the comparison between the analytical results obtained by the proposed model and a particular problem already discussed in literature for a stress-free gel membrane (one-dimensional test case) will highlight the relevance of the derived model.
聚合物凝胶是多孔的、充满流体的材料,可在各种刺激下膨胀或收缩。由膨胀/收缩引起的变形会产生较大应力,这可能导致材料失效。在本研究中,采用非线性应力扩散模型来研究水合受限聚合物凝胶在化学势变化时产生的应力和变形状态。考虑了两种不同的约束构型:(i) 沿厚度方向的弹性约束和 (ii) 平面弹性约束。第一步完全定义了压缩/拉伸构型。在此基础上,进行了增量化学-力学分析。所推导的模型相对于预应力构型扩展了经典的线性多孔弹性理论。最后,将所提出模型得到的分析结果与文献中已讨论的无应力凝胶膜特定问题(一维测试案例)进行比较,将突出所推导模型的相关性。