Characterizing hydrogel behavior under compression with gel-freezing osmometry

Fuente: arXiv
Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Feng, Yanxia, Gerber, Dominic, Heyden, Stefanie, Kröger, Martin, Dufresne, Eric R., Isa, Lucio, Style, Robert W.
Format: Preprint
Veröffentlicht: 2024
Schlagworte:
Online-Zugang:
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
_version_ 1866911960888508416
author Feng, Yanxia
Gerber, Dominic
Heyden, Stefanie
Kröger, Martin
Dufresne, Eric R.
Isa, Lucio
Style, Robert W.
author_facet Feng, Yanxia
Gerber, Dominic
Heyden, Stefanie
Kröger, Martin
Dufresne, Eric R.
Isa, Lucio
Style, Robert W.
contents Hydrogels are particularly versatile materials that are widely found in both Nature and industry. One key reason for this versatility is their high water content, which lets them dramatically change their volume and many of their mechanical properties -- often by orders of magnitude -- as they swell and dry out. Currently, we lack techniques that can precisely characterize how these properties change with water content. To overcome this challenge, here we develop Gel-Freezing Osmometry (GelFrO): an extension of freezing-point osmometry. We show how GelFrO can measure a hydrogel's mechanical response to compression and osmotic pressure, while only using small, $O(100μ$L$)$ samples. Because the technique allows measurement of properties over an unusually wide range of water contents, it allows us to accurately test theoretical predictions. We find simple, power-law behavior for both mechanical response to compression, and osmotic pressure, while these are not well-captured by classical Flory-Huggins theory. We interpret this power-law behavior as a hallmark of a microscopic fractal structure of the gel's polymer network, and propose a simple way to connect the gel's fractal dimension to its mechanical and osmotic properties. This connection is supported by observations of hydrogel microstructures using small-angle x-ray scattering. Finally, our results motivate us to propose an updated constitutive model describing hydrogel swelling, and mechanical response.
format Preprint
id arxiv_https___arxiv_org_abs_2407_13718
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Characterizing hydrogel behavior under compression with gel-freezing osmometry
Feng, Yanxia
Gerber, Dominic
Heyden, Stefanie
Kröger, Martin
Dufresne, Eric R.
Isa, Lucio
Style, Robert W.
Soft Condensed Matter
Materials Science
Hydrogels are particularly versatile materials that are widely found in both Nature and industry. One key reason for this versatility is their high water content, which lets them dramatically change their volume and many of their mechanical properties -- often by orders of magnitude -- as they swell and dry out. Currently, we lack techniques that can precisely characterize how these properties change with water content. To overcome this challenge, here we develop Gel-Freezing Osmometry (GelFrO): an extension of freezing-point osmometry. We show how GelFrO can measure a hydrogel's mechanical response to compression and osmotic pressure, while only using small, $O(100μ$L$)$ samples. Because the technique allows measurement of properties over an unusually wide range of water contents, it allows us to accurately test theoretical predictions. We find simple, power-law behavior for both mechanical response to compression, and osmotic pressure, while these are not well-captured by classical Flory-Huggins theory. We interpret this power-law behavior as a hallmark of a microscopic fractal structure of the gel's polymer network, and propose a simple way to connect the gel's fractal dimension to its mechanical and osmotic properties. This connection is supported by observations of hydrogel microstructures using small-angle x-ray scattering. Finally, our results motivate us to propose an updated constitutive model describing hydrogel swelling, and mechanical response.
title Characterizing hydrogel behavior under compression with gel-freezing osmometry
topic Soft Condensed Matter
Materials Science
url https://arxiv.org/abs/2407.13718