Paper Number
GG45
Session
Rheology of Gels, Glasses and Jammed Systems
Title
A generalized memory function based on recoverable strain and its relation to nanoscale structure
Presentation Date and Time
October 12, 2022 (Wednesday) 2:50
Track / Room
Track 3 / Sheraton 5
Authors
- Kamani, Krutarth M. (University of Illinois at Urbana-Champaign, Department of Chemical and Biomolecular Engineering)
- Shim, Yul Hui (University of Illinois at Urbana-Champaign, Department of Chemical and Biomolecular Engineering)
- Griebler, James (University of Illinois at Urbana-Champaign, Department of Chemical and Biomolecular Engineering)
- Narayanan, Suresh (Argonne National Laboratory, Advanced Photon Source)
- Zhang, Qingteng (Argonne National Laboratory, Advanced Photon Source)
- Rogers, Simon A. (University of Illinois at Urbana-Champaign, Department of Chemical and Biomolecular Engineering)
Author and Affiliation Lines
Krutarth M. Kamani1, Yul Hui Shim1, James Griebler1, Suresh Narayanan2, Qingteng Zhang2 and Simon A. Rogers1
1Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801; 2Advanced Photon Source, Argonne National Laboratory, Lemont, IL 60439
Speaker / Presenter
Rogers, Simon A.
Keywords
experimental methods; theoretical methods; colloids; gels; glasses; jammed systems; microscopy; rheometry techniques; spectroscopy
Text of Abstract
The physics behind the mechanism of memory formation and loss in soft materials is of great interest to understanding the behavior of biological, environmental, and industrial materials. The traditional rheological memory function quantifies the rate at which memory is lost and assumes that the memory originates from application of a step strain, making it difficult to apply to arbitrary transient rheological protocols. Recent studies of memory apply cyclic shearing and implement a stroboscopic protocol for determining differences and similarities in structural measures but have yet to connect the transient rheology to memory formation and loss. In this work, we propose a generalized memory function and apply it to the analysis of rheo-X-ray photon correlation spectroscopy (rheo-XPCS) experimental data from an aggregated fumed silica gel and predictions from a continuum model under dynamic shearing. Our proposal is defined in terms of changes in the ultimate recoverable strain over an interval and includes the traditional definition of memory in response to a small step strain, but generalizes it to any linear or nonlinear deformation or loading protocol, allowing for the determination of when and how quickly memories are imparted and forgotten. Our rheo-XPCS data show that the aggregate-level structure recorrelates whenever the change in recoverable strain over some interval is zero. The macroscopic recoverable strain is therefore a measure of the nano-scale structural memory. We further show that the magnitude of the structural recorrelation determined in rheo-XPCS is proportional to how much of the applied strain is recoverable. We therefore equate the property of memory with the behavior of recovery. Our proposed memory function is generic, as it can be equally applied to any soft materials under any deformation protocol. This work emphasizes the critical role of recoverable strain in connecting structural measures to bulk rheological responses.