4.7 Article

Viscoelastic phase separation model for ternary polymer solutions

Journal

JOURNAL OF CHEMICAL PHYSICS
Volume 154, Issue 10, Pages -

Publisher

AMER INST PHYSICS
DOI: 10.1063/5.0039208

Keywords

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Funding

  1. JSPS KAKENHI [19H01862]
  2. Grants-in-Aid for Scientific Research [19H01862] Funding Source: KAKEN

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The study reveals that viscoelastic phase separation in polymer solutions leads to a network-like structure in ternary systems, with the solvent able to freely move between the polymer-rich and water-rich phases during phase separation. These findings are important for understanding the phase separation mechanism of ternary mixtures commonly used in the manufacturing of polymeric separation membranes.
When a polymer solution undergoes viscoelastic phase separation, the polymer-rich phase forms a network-like structure even if it is a minor phase. This unique feature is induced by polymer dynamics, which are constrained by the temporal entanglement of polymer chains. The fundamental mechanisms of viscoelastic phase separation have already been elucidated by theory and experiments over the past few decades; however, it is not yet well understood how viscoelastic phase separation occurs in multicomponent polymer solutions. Here, we construct a new viscoelastic phase separation model for ternary polymer solutions that consist of a polymer, solvent, and nonsolvent. Our simulation results reveal that a network-like structure is formed in the ternary bulk system through a phase separation mechanism similar to that observed in binary polymer solutions. A difference in dynamics is also found in that the solvent, whose affinity to the polymer is similar to that of the nonsolvent, moves freely between the polymer-rich and water-rich phases during phase separation. These findings are considered important for understanding the phase separation mechanism of ternary mixtures often used in the manufacture of polymeric separation membranes.

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