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Published on: February 6, 2014
Kinetics of Shear-Induced Structural Ordering in Dense Colloids
HongRui He1,2, Jonghun Lee3, Zhang Jiang3
1Materials Science Division and Center for Molecular Engineering, Argonne National Laboratory, Argonne, Illinois 60439, United States.
Abstract:
The macroscopic rheological response of a colloidal solution is highly correlated with the local microscopic structure, as revealed by an in situ Rheo-SAXS experiment with a high temporal resolution. Oscillatory shear can induce a strain-controlled ordering-to-disorder transition, resulting in a shear-thickening process that is different from the normal shear-thickening behavior that is driven by hydrodynamics and particle friction. We reveal that there is a complex time-dependent kinetics toward structural ordering under different applied strains. When the strain amplitude reaches a critical value that starts to induce disordering in the system, the pathway toward the dynamic equilibrium can also become highly non-monotonic. Within the same oscillatory cycle, there is a strong correlation of ordering with different phases of the oscillation, with the system oscillating between two dynamic metastable states.
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