Unraveling the Role of Order-to-Disorder Transition in Shear Thickening Suspensions

Jonghun Lee, Zhang Jiang, Jin Wang, Alec R. Sandy, Suresh Narayanan, and Xiao-Min Lin
Phys. Rev. Lett. 120, 028002 – Published 9 January 2018
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Abstract

Using high-resolution in situ small angle x-ray scattering in conjunction with oscillatory shear on highly monodisperse silica suspensions, we demonstrate that an order-to-disorder transition leads to a dynamic shear thickening in a lower stress regime than the standard steady shear thickening. We show that the order-to-disorder transition is controlled by strain, which is distinguishably different from steady shear thickening, which is a stress-related phenomenon. The appearance of this two-step shear thinning and thickening transition is also influenced by the particle size, monodispersity, and measurement conditions (i.e., oscillatory shear versus steady shear). Our results show definitively that the order-to-disorder transition-induced thickening is completely unrelated to the mechanism that drives steady shear thickening.

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  • Received 2 May 2017
  • Revised 16 November 2017

DOI:https://doi.org/10.1103/PhysRevLett.120.028002

© 2018 American Physical Society

Physics Subject Headings (PhySH)

Polymers & Soft Matter

Authors & Affiliations

Jonghun Lee, Zhang Jiang, Jin Wang, Alec R. Sandy, and Suresh Narayanan*

  • Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois 60439, USA

Xiao-Min Lin

  • Center for Nanoscale Materials, Argonne National Laboratory, Argonne, Illinois 60439, USA

  • *sureshn@anl.gov
  • xmlin@anl.gov

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Issue

Vol. 120, Iss. 2 — 12 January 2018

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