Reversal of Solvent Migration in Poroelastic Folds

dc.contributor.authorFlapper, Mees M.
dc.contributor.authorPandey, Anupam
dc.contributor.authorEssink, Martin H.
dc.contributor.authorvan Brummelen, E. Harald
dc.contributor.authorKarpitschka, Stefan
dc.contributor.authorSnoeijer, Jacco H.
dc.date.accessioned2024-11-21T08:47:57Z
dc.date.available2024-11-21T08:47:57Z
dc.date.issued2023-06-02
dc.description.abstractPolymer networks and biological tissues are often swollen by a solvent such that their properties emerge from a coupling between swelling and elastic stress. This poroelastic coupling becomes particularly intricate in wetting, adhesion, and creasing, for which sharp folds appear that can even lead to phase separation. Here, we resolve the singular nature of poroelastic surface folds and determine the solvent distribution in the vicinity of the fold tip. Surprisingly, two opposite scenarios emerge depending on the angle of the fold. In obtuse folds such as creases, it is found that the solvent is completely expelled near the crease tip, according to a nontrivial spatial distribution. For wetting ridges with acute fold angles, the solvent migration is reversed as compared to creasing, and the degree of swelling is maximal at the fold tip. We discuss how our poroelastic fold analysis offers an explanation for phase separation, fracture, and contact angle hysteresis.
dc.description.versionpublisheddeu
dc.identifier.doi10.1103/physrevlett.130.228201
dc.identifier.ppn1910590436
dc.identifier.urihttps://kops.uni-konstanz.de/handle/123456789/71371
dc.language.isoeng
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.ddc530
dc.titleReversal of Solvent Migration in Poroelastic Foldseng
dc.typeJOURNAL_ARTICLE
dspace.entity.typePublication
kops.citation.bibtex
@article{Flapper2023-06-02Rever-71371,
  year={2023},
  doi={10.1103/physrevlett.130.228201},
  title={Reversal of Solvent Migration in Poroelastic Folds},
  number={22},
  volume={130},
  issn={0031-9007},
  journal={Physical Review Letters},
  author={Flapper, Mees M. and Pandey, Anupam and Essink, Martin H. and van Brummelen, E. Harald and Karpitschka, Stefan and Snoeijer, Jacco H.},
  note={Article Number: 228201}
}
kops.citation.iso690FLAPPER, Mees M., Anupam PANDEY, Martin H. ESSINK, E. Harald VAN BRUMMELEN, Stefan KARPITSCHKA, Jacco H. SNOEIJER, 2023. Reversal of Solvent Migration in Poroelastic Folds. In: Physical Review Letters. American Physical Society (APS). 2023, 130(22), 228201. ISSN 0031-9007. eISSN 1079-7114. Verfügbar unter: doi: 10.1103/physrevlett.130.228201deu
kops.citation.iso690FLAPPER, Mees M., Anupam PANDEY, Martin H. ESSINK, E. Harald VAN BRUMMELEN, Stefan KARPITSCHKA, Jacco H. SNOEIJER, 2023. Reversal of Solvent Migration in Poroelastic Folds. In: Physical Review Letters. American Physical Society (APS). 2023, 130(22), 228201. ISSN 0031-9007. eISSN 1079-7114. Available under: doi: 10.1103/physrevlett.130.228201eng
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    <dcterms:abstract>Polymer networks and biological tissues are often swollen by a solvent such that their properties emerge from a coupling between swelling and elastic stress. This poroelastic coupling becomes particularly intricate in wetting, adhesion, and creasing, for which sharp folds appear that can even lead to phase separation. Here, we resolve the singular nature of poroelastic surface folds and determine the solvent distribution in the vicinity of the fold tip. Surprisingly, two opposite scenarios emerge depending on the angle of the fold. In obtuse folds such as creases, it is found that the solvent is completely expelled near the crease tip, according to a nontrivial spatial distribution. For wetting ridges with acute fold angles, the solvent migration is reversed as compared to creasing, and the degree of swelling is maximal at the fold tip. We discuss how our poroelastic fold analysis offers an explanation for phase separation, fracture, and contact angle hysteresis.</dcterms:abstract>
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kops.sourcefield.plainPhysical Review Letters. American Physical Society (APS). 2023, 130(22), 228201. ISSN 0031-9007. eISSN 1079-7114. Available under: doi: 10.1103/physrevlett.130.228201eng
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