Systematic derivation of hydrodynamic equations for viscoelastic phase separation.

GENERIC Poisson brackets coarse-graining rheology two-fluid model viscoelastic phase separation

Journal

Journal of physics. Condensed matter : an Institute of Physics journal
ISSN: 1361-648X
Titre abrégé: J Phys Condens Matter
Pays: England
ID NLM: 101165248

Informations de publication

Date de publication:
08 Jul 2021
Historique:
received: 22 12 2020
accepted: 21 06 2021
pubmed: 22 6 2021
medline: 22 6 2021
entrez: 21 6 2021
Statut: epublish

Résumé

We present a detailed derivation of a simple hydrodynamic two-fluid model, which aims at the description of the phase separation of non-entangled polymer solutions, where viscoelastic effects play a role. It is directly based upon the coarse-graining of a well-defined molecular model, such that all degrees of freedom have a clear and unambiguous molecular interpretation. The considerations are based upon a free-energy functional, and the dynamics is split into a conservative and a dissipative part, where the latter satisfies the Onsager relations and the second law of thermodynamics. The model is therefore fully consistent with both equilibrium and non-equilibrium thermodynamics. The derivation proceeds in two steps: firstly, we derive an extended model comprising two scalar and four vector fields, such that inertial dynamics of the macromolecules and of the relative motion of the two fluids is taken into account. In the second step, we eliminate these inertial contributions and, as a replacement, introduce phenomenological dissipative terms, which can be modeled easily by taking into account the principles of non-equilibrium thermodynamics. The final simplified model comprises the momentum conservation equation, which includes both interfacial and elastic stresses, a convection-diffusion equation where interfacial and elastic contributions occur as well, and a suitably convected relaxation equation for the end-to-end vector field. In contrast to the traditional two-scale description that is used to derive rheological equations of motion, we here treat the hydrodynamic and the macromolecular degrees of freedom on the same basis. Nevertheless, the resulting model is fairly similar, though not fully identical, to models that have been discussed previously. Notably, we find a rheological constitutive equation that differs from the standard Oldroyd-B model. Within the framework of kinetic theory, this difference may be traced back to a different underlying statistical-mechanical ensemble that is used for averaging the stress. To what extent the model is able to reproduce the full phenomenology of viscoelastic phase separation is presently an open question, which shall be investigated in the future.

Identifiants

pubmed: 34153954
doi: 10.1088/1361-648X/ac0d17
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Creative Commons Attribution license.

Auteurs

Dominic Spiller (D)

Max Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.

Aaron Brunk (A)

Institute of Mathematics, Johannes Gutenberg University Mainz, Staudingerweg 9, 55128 Mainz, Germany.

Oliver Habrich (O)

Department of Mathematics, Technical University Darmstadt, Dolivostraße 15, 64293 Darmstadt, Germany.

Herbert Egger (H)

Department of Mathematics, Technical University Darmstadt, Dolivostraße 15, 64293 Darmstadt, Germany.

Mária Lukáčová-Medvid'ová (M)

Institute of Mathematics, Johannes Gutenberg University Mainz, Staudingerweg 9, 55128 Mainz, Germany.

Burkhard Dünweg (B)

Max Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.
Department of Chemical Engineering, Monash University, Clayton, Victoria 3800, Australia.

Classifications MeSH