Issue 29, 2024

Relationship between πA isotherms and single microgel/microgel array structures revealed via the direct visualization of microgels at the air/water interface

Abstract

The structures of single microgels and microgel arrays formed at the air/water interface were visualized directly, and their structures correlated with πA isotherms in order to understand the compression behavior of soft and deformable microgels at this interface. Large microgels (ca. 4 μm) were synthesized so that these can be clearly visualized at the air/water interface, even under high compression, and a series of microgel compression experiments were directly evaluated using a Langmuir trough equipped with a fluorescence microscope. The experiments revealed that upon compressing the microgel arrays at the interface voids disappeared and colloidal crystallinity increased. However, the colloidal crystallinity decreased when the microgel arrays were strongly compressed. In addition, when the structures were observed at higher magnification, it became clear that the single microgel structures, when visualized from above, changed from circular to polygonal upon compressing the microgel array. The results of this study can be expected to improve the understanding of the compression behavior of microgel arrays adsorbed at the air/water interface and will thus be useful for the creation of new functional microgel stabilizers with potential applications in e.g., bubbles and emulsions.

Graphical abstract: Relationship between π–A isotherms and single microgel/microgel array structures revealed via the direct visualization of microgels at the air/water interface

Supplementary files

Article information

Article type
Paper
Submitted
27 May 2024
Accepted
09 Jul 2024
First published
15 Jul 2024
This article is Open Access
Creative Commons BY-NC license

Soft Matter, 2024,20, 5836-5847

Relationship between πA isotherms and single microgel/microgel array structures revealed via the direct visualization of microgels at the air/water interface

T. Kawamoto, H. Minato and D. Suzuki, Soft Matter, 2024, 20, 5836 DOI: 10.1039/D4SM00640B

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