粘弹性
高原(数学)
类型(生物学)
流变学
锂长石
谱线
胶体
化学物理
聚合物
材料科学
边界(拓扑)
化学
热力学
边值问题
凝聚态物理
矿物学
分子物理学
系列(地层学)
变形(气象学)
光谱(功能分析)
空格(标点符号)
增长率
物理
高分子化学
作者
Wei Wu,Yingkang Dai,Weixiang Sun,Tao Wang,Zhen TONG
标识
DOI:10.1002/marc.202500897
摘要
We distinguish two rheological routes to the liquid-solid transition (LST) in soft materials by tracking the linear viscoelastic spectrum under small-amplitude oscillatory shear. Type I (dynamical arrest) shows the growth of a low-frequency elastic plateau without a reversal in the loss-tangent trend; Type II (percolation with criticality) features scale-free spectra at a well-defined time and a reversal in the loss-tangent trend. In synthetic hectorite suspensions spanning broad clay and salt concentrations, freshly prepared samples consistently follow Type II. After aging and pre-shear, the pathway becomes history-dependent: a map in composition-shear space reveals a boundary where high clay concentrations undergo Type I only, whereas lower clay concentrations evolve from Type I to Type II; increasing pre-shear rate shifts this boundary to higher clay content. A unified mechanism links these routes to aggregation kinetics: early particle-cluster growth yields peaked cluster-size distributions and Type I arrest; later depletion-enhanced cluster-cluster aggregation produces heavy-tailed distributions and Type II percolation. These results explain why "shear rejuvenation" does not restore the fresh state and provide a spectrum-based framework relevant to colloids and polymer systems undergoing physical or chemical gelation.
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