Bonn D, Kellay H, Prochnow M, Ben-Djemiaa K, Meunier J
D. Bonn, M. Prochnow, K. Ben-Djemiaa, J. Meunier, Laboratoire de Physique Statistique de l'Ecole Normale Superieure, 24 rue Lhomond, 75231 Paris Cedex 05, France. H. Kellay, Centre de Physique Moleculaire Optique et Hertzienne, Universit
Science. 1998 Apr 10;280(5361):265-7. doi: 10.1126/science.280.5361.265.
The spontaneous fracture of polymer gels was studied. Contrary to crystalline solids, where fracture usually happens instantaneously at a well-defined breaking strength, the fracture of a polymer gel can occur with a delay. When a constant force was applied, the cracks nucleated and started to propagate after a delay that can be as long as 15 minutes, depending on the force. This phenomenon can be understood by calculating the activation energy for crack nucleation in arbitrary dimension and accounting for the inhomogeneity of the gel network in terms of its fractal dimension.
对聚合物凝胶的自发断裂进行了研究。与晶体固体不同,晶体固体的断裂通常在明确的断裂强度下瞬间发生,而聚合物凝胶的断裂可能会有延迟。当施加恒定力时,裂纹会在延迟后成核并开始扩展,延迟时间可能长达15分钟,这取决于力的大小。通过计算任意维度下裂纹成核的活化能,并根据凝胶网络的分形维数考虑其不均匀性,可以理解这一现象。