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Cyclically sheared colloidal gels: structural change and delayed failure time.

Himangsu Bhaumik1, James E Hallett2, Tanniemola B Liverpool3

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Summary
This summary is machine-generated.

Cyclically shearing colloidal gels alters their structure and mechanical properties. Depending on shear conditions, gels can become more compliant (thixotropy) or stiffer (strain hardening), impacting their stability.

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Area of Science:

  • Colloidal science
  • Soft matter physics
  • Materials science

Background:

  • Colloidal gels are complex fluids with applications in food, cosmetics, and pharmaceuticals.
  • Understanding their response to mechanical stress is crucial for processing and stability.

Purpose of the Study:

  • To investigate the structural and mechanical changes in colloidal gels under cyclic shear.
  • To explore the relationship between shear history and gel behavior, including thixotropy and strain hardening.

Main Methods:

  • Experimental studies on colloid-polymer mixture gels.
  • Computer simulations using a model gel-former.
  • Analysis of structural parameters (topological cluster classification, bond-order parameters, pore size distribution).
  • Mechanical response analysis (stress, dissipation rate, creeping flow).

Main Results:

  • Cyclic shear induces structural evolution and pore size increase in gels.
  • A crossover from elastic to plastic behavior is observed with increasing strain amplitude.
  • Gels exhibit both thixotropy (increased compliance) and strain hardening (reduced compliance) depending on parameters.
  • Pre-sheared gels show increased stability under constant shear stress.
  • Anisotropic structural features are imprinted by cyclic shear, influencing response orientation.

Conclusions:

  • Cyclic shear significantly modifies colloidal gel microstructure and rheology.
  • The observed thixotropy and strain hardening are key responses to shear history.
  • Anisotropy introduced by cyclic shear plays a critical role in gel stability and flow behavior.