Granular Hydrogels as Brittle Yield Stress Fluids

G Gunnar B. Thompson (Dept. Chemical and Biomolecular Engineering University of Illinois Urbana‐Champaign 600 S Mathews Ave Urbana IL 61801 USA) J Jiye Lee K Krutarth M. Kamani (Dept. Chemical and Biomolecular Engineering University of Illinois Urbana‐Champaign 600 S Mathews Ave Urbana IL 61801 USA) N Noah Flores‐Velasco (Dept. Chemical and Biomolecular Engineering University of Illinois Urbana‐Champaign 600 S Mathews Ave Urbana IL 61801 USA) S Simon A. Rogers (Dept. Chemical and Biomolecular Engineering University of Illinois Urbana‐Champaign 600 S Mathews Ave Urbana IL 61801 USA) B Brendan A. C. Harley (Dept. Chemical and Biomolecular Engineering University of Illinois Urbana‐Champaign 600 S Mathews Ave Urbana IL 61801 USA)

Abstract

Abstract While granular hydrogels are increasingly used in biomedical applications, methods to capture their rheological behavior generally consider shear‐thinning and self‐healing properties or produce ensemble metrics (e.g., dynamic moduli) while neglecting transient yielding and unyielding processes. Combining oscillatory shear testing with Brittility (Bt) via the Kamani‐Donley‐Rogers (KDR) model, this work shows that granular hydrogels behave as brittle yield stress fluids. This work quantifies steady and transient rheology as a function of microgel properties and granular composition for polyethylene glycol and gelatin microgels. The KDR model with Bt captures granular hydrogel behavior for a wide range of design parameters, reducing the complex rheology to a determination of model parameters. In granular mixtures, this work observes monotonic dependencies of the elastic modulus, structural viscosity, and brittility upon granular composition, while the yield stress is lower for mixtures. Microgel size distribution and polymer fraction are the most influential parameters in monolithic granular hydrogels, while microgel size and packing density are less impactful. The model robustly captures self‐healing behavior and reveals that granular hydrogel relaxation accelerates with an increased small‐amplitude strain rate. This quantitative framework is an important step toward rational design of granular hydrogels for applications ranging from injection and in situ stabilization to 3D bioprinting.

Article Details

Volume / Issue Vol. 37, Issue 39
Published October 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (6)

G

Gunnar B. Thompson

Dept. Chemical and Biomolecular Engineering University of Illinois Urbana‐Champaign 600 S Mathews Ave Urbana IL 61801 USA

J

Jiye Lee

K

Krutarth M. Kamani

Dept. Chemical and Biomolecular Engineering University of Illinois Urbana‐Champaign 600 S Mathews Ave Urbana IL 61801 USA

N

Noah Flores‐Velasco

Dept. Chemical and Biomolecular Engineering University of Illinois Urbana‐Champaign 600 S Mathews Ave Urbana IL 61801 USA

S

Simon A. Rogers

Dept. Chemical and Biomolecular Engineering University of Illinois Urbana‐Champaign 600 S Mathews Ave Urbana IL 61801 USA

B

Brendan A. C. Harley

Dept. Chemical and Biomolecular Engineering University of Illinois Urbana‐Champaign 600 S Mathews Ave Urbana IL 61801 USA