Tsurusawa Hideyo, Leocmach Mathieu, Russo John, Tanaka Hajime
Department of Fundamental Engineering, Institute of Industrial Science, University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8505, Japan.
Université de Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière, F-69622 Villeurbanne, France.
Sci Adv. 2019 May 31;5(5):eaav6090. doi: 10.1126/sciadv.aav6090. eCollection 2019 May.
Colloidal gels have unique mechanical and transport properties that stem from their bicontinuous nature, in which a colloidal network is intertwined with a viscous solvent, and have found numerous applications in foods, cosmetics, and construction materials and for medical applications, such as cartilage replacements. So far, our understanding of the process of colloidal gelation is limited to long-time dynamical effects, where gelation is viewed as a phase separation process interrupted by the glass transition. However, this purely out-of-equilibrium thermodynamic picture does not address the emergence of mechanical stability. With confocal microscopy experiments, we reveal that mechanical metastability is reached only after isotropic percolation of locally isostatic environments, establishing a direct link between the load-bearing ability of gels and the isostaticity condition. Our work suggests an operative description of gels based on mechanical equilibrium and isostaticity, providing the physical basis for the stability and rheology of these materials.
胶体凝胶具有独特的力学和传输特性,这些特性源于其双连续性质,即胶体网络与粘性溶剂相互交织,并且在食品、化妆品、建筑材料以及医疗应用(如软骨替代)中有着众多应用。到目前为止,我们对胶体凝胶化过程的理解仅限于长时间的动力学效应,在这种效应中,凝胶化被视为由玻璃化转变中断的相分离过程。然而,这种纯粹的非平衡热力学图景并未涉及机械稳定性的出现。通过共聚焦显微镜实验,我们揭示了只有在局部各向同性环境的各向同性渗流之后才会达到机械亚稳性,从而在凝胶的承载能力和各向同性条件之间建立了直接联系。我们的工作提出了一种基于机械平衡和各向同性的凝胶作用描述,为这些材料的稳定性和流变学提供了物理基础。