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Surface structure, mechanics and rheology of amphiphilic polymer conetworks on different length scales

POSTER

Abstract

In order to allow the simultaneous transport of hydrophilic and hydrophobic substances, networks with fine-structured hydrophilic and hydrophobic components are requested. Amphiphilic polymer co-networks (ACNs) can be tailored to create gels that selectively swell or collapse in different solvents with the corresponding polarity and greatly impact transport properties through these networks.

This study focuses on the relation between structure, swelling abilities and mechanical/rheological properties of films of ACNs.1,2 First, the correlation between different synthesis strategies for gel films and their resulting properties will be described. Secondly, the effect of solvents of different polarity on the swelling ability will be presented on different length scales. For this purpose, topology and near surface structure are studied with atomic force microscopy (AFM). We also put special emphasis on the determination of mechanical and rheological properties laterally and orthogonally to the gel surface by carrying out dynamic AFM indentation experiments. In order to evaluate heterogeneities the mechanical and rheological behavior at the interface of the ACNs will be presented on various length scales (nm - µm). The study shows that the synthesis strategy has a strong effect on the gel structure and on nano/microrheological properties. The structure and rheology of gel films will be compared with results obtained of the respective bulk gel phase.

Publication: [1] Bunk et al., Amphiphilic Model Networks Based on PEG and PCL Tetra-arm Star Polymers with Complementary Reactivity, Macromolecules 2022, 55, 15, 6573–6589.<br>[2] Hagmann et al., Amphiphilic Polymer Conetwork Gel Films Based on Tetra-Poly(ethylene Glycol) and Tetra-Poly(e-Caprolactone), Polymers 2022, 14, 13, 2555.<br>

Presenters

  • Kevin Hagmann

    Technische Universitat Darmstadt

Authors

  • Kevin Hagmann

    Technische Universitat Darmstadt

  • Nora Fribiczer

    Department of Chemistry, Johannes Gutenberg University Mainz, D-55128 Mainz, Johannes Gutenberg University Mainz, Department of Chemistry, Duesbergweg 10-14, D-55128 Mainz, Germany

  • Sebastian Seiffert

    Department of Chemistry, Johannes Gutenberg University Mainz, D-55128 Mainz, Johannes Gutenberg University Mainz, Department of Chemistry, Duesbergweg 10-14, D-55128 Mainz, Germany

  • Carolin Bunk

    Leibniz-Institut für Polymerforschung Dresden e.V., D-01069 Dresden, Leibniz-Institut für Polymerforschung Dresden e.V, D-01069 Dresden, Leibniz Institut für Polymerforschung, Hohe Straße 6, 01069 Dresden, Germany. Organic Chemistry of Polymers, Technische Universität Dresden, 01062 Dresden, Germany

  • Frank Böhme

    Leibniz-Institut für Polymerforschung Dresden e.V., D-01069 Dresden, Leibniz Institut für Polymerforschung, Hohe Straße 6, 01069 Dresden, Germany

  • Regine von Klitzing

    Institute for Condensed Matter Physics, Technische Universität Darmstadt, D-64289 Darmstadt, Institute for Condensed Matter Physics, Technische Universität Darmstadt