Department of Mechanical Engineering, McGill University, Montreal, QC H3A 0C3, Canada.
Department of Biomedical Engineering, McGill University, Montreal, QC H3A 0C3, Canada.
ACS Macro Lett. 2021 Feb 16;10(2):180-185. doi: 10.1021/acsmacrolett.0c00854. Epub 2021 Jan 12.
Tough adhesive hydrogels find broad applications in engineering and medicine. Such hydrogels feature high resistance against both cohesion and adhesion failure. The superior fracture properties may, however, deteriorate when the hydrogels swell upon exposure of water. The underlying correlation between the polymer fraction and fracture properties of tough adhesive hydrogels remains largely unexplored. Here, we study how the cohesion and adhesion energies of a tough adhesive hydrogel evolve with the swelling process. The results show a similar scaling law (ϕ) of the two quantities as a function of the polymer fraction (ϕ). Our scaling analysis and computational study reveal that it stems from the scaling of shear modulus. The study will promote the investigation of scaling of hydrogel fracture and provide development guidelines for next-generation tough adhesive hydrogels.
坚韧的黏附水凝胶在工程和医学领域有广泛的应用。此类水凝胶具有高抗内聚和抗黏附破坏的能力。然而,当水凝胶暴露于水中而发生溶胀时,其优异的断裂性能可能会恶化。目前,关于坚韧的黏附水凝胶的聚合物分数与断裂性能之间的相关性还知之甚少。在这里,我们研究了坚韧的黏附水凝胶的内聚能和黏附能如何随溶胀过程而变化。结果表明,这两个量与聚合物分数(ϕ)之间存在相似的标度律(ϕ)。我们的标度分析和计算研究表明,这源于剪切模量的标度。该研究将促进对水凝胶断裂的标度研究,并为下一代坚韧的黏附水凝胶的开发提供指导。