Phase behavior of silica-PNIPAm nanogels under high hydrostatic pressure

The structure and dynamics of concentrated silica-PNIPAm (poly-<i>N</i>-iso-prop-yl-acrylamide) nanogels are studied as a function of hydrostatic pressure up to 3500 bar. A combination of X-ray photon correlation spectroscopy and small-angle X-ray scattering shows similar characteristics of the dynamics for both temperature- and pressure-induced volume phase transitions of PNIPAm nanogels. Upon increasing the pressure and depending on the initial particle volume fraction, a transition from a liquid or glass state to a colloidal gel is observed for pressures <i>p</i> ≃ 1500 bar at a temperature of 293 K. Time-dependent analysis of the dynamics shows aging in glass and gel samples which is absent in the liquid state. This indicates stress-dominated dynamics upon pressure changes that equilibrate after a few hundred seconds.

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Publication Details

Journal
Journal of Applied Crystallography
Published
2025-04-29
DOI
https://doi.org/10.1107/s1600576725003188
Citations
1
Primary Topic
Mesoporous Materials and Catalysis
Type
article
Field-Weighted Citation Impact
0.52

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article

Phase behavior of silica-PNIPAm nanogels under high hydrostatic pressure

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Journal of Applied Crystallography
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article

Phase behavior of silica-PNIPAm nanogels under high hydrostatic pressure

Christina Krywka, Claudia Goy, Niels C. Gießelmann, Nele N. Striker, Svenja C. Hövelmann, Florian Schulz, Michael Paulus, Irina Lokteva, Frédéric Caupin, Fabian Westermeier, Felix Lehmkühler
article en
1 citations

Abstract

The structure and dynamics of concentrated silica-PNIPAm (poly-<i>N</i>-iso-prop-yl-acrylamide) nanogels are studied as a function of hydrostatic pressure up to 3500 bar. A combination of X-ray photon correlation spectroscopy and small-angle X-ray scattering shows similar characteristics of the dynamics for both temperature- and pressure-induced volume phase transitions of PNIPAm nanogels. Upon increasing the pressure and depending on the initial particle volume fraction, a transition from a liquid or glass state to a colloidal gel is observed for pressures <i>p</i> ≃ 1500 bar at a temperature of 293 K. Time-dependent analysis of the dynamics shows aging in glass and gel samples which is absent in the liquid state. This indicates stress-dominated dynamics upon pressure changes that equilibrate after a few hundred seconds.

Journal of Applied CrystallographyVol. 58(3)
Université Claude Bernard Lyon 1 (FR), Centre National de la Recherche Scientifique (FR), Universität Hamburg (DE), TU Dortmund University (DE), Deutsches Elektronen-Synchrotron DESY (DE), Hochschule für Angewandte Wissenschaften Kiel (DE), Institut Lumière Matière (FR), Helmholtz-Zentrum Hereon (DE), Max Planck Institute for the Structure and Dynamics of Matter (DE), Hamburg Centre for Ultrafast Imaging
Deutsches Elektronen-Synchrotron
Openalex Percentile: Top 38%
Mesoporous Materials and Catalysis
0.52
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