Abstract
A correct description of phase behaviour in polymer solutions requires a coupling between configurational statistics and thermodynamics. The effect of flow-induced chain deformation on the polymer-solvent interaction energy depends on the concentration and on the polymer architecture. It will be demonstrated, using thermodynamic arguments, that for linear polymers this may give rise to a large flow-induced demixing. For more complex architectures such as ring polymers and branched polymers, a maximum in the critical temperature vs. flow rate is predicted.
Original language | English (US) |
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Pages (from-to) | 407-412 |
Number of pages | 6 |
Journal | Europhysics Letters |
Volume | 42 |
Issue number | 4 |
DOIs | |
State | Published - May 15 1998 |
ASJC Scopus subject areas
- General Physics and Astronomy