Arrested mobility and thermal fluctuation effects on the mass transfer induced phase separation of ternary polymer solutions

ORAL

Abstract

Many polymer membranes are made by immersion of a polymer solution film in a nonsolvent bath: the mass transfer exchange between the nonsolvent from the bath and the solvent in the film induces phase separation of the film into a polymer-rich phase that becomes the membrane matrix and a polymer-poor phase that becomes the membrane pores. Microstructure formation of these membranes is still not fully understood due to the nature of the physical processes involved: the mass transfer induced phase separation, the coarsening of domains, and the vitrification of the polymer-rich phase that arrests membrane microstructure. In this work, we use phase-field models of the ternary polymer-nonsolvent-solvent system to solve the coupled convection-diffusion and momentum equations that describe membrane formation. We model the glass transition using contrasts in the viscosity and mobility of the polymer-rich and polymer-poor phases. We report how glassy dynamics, and the inclusion of thermal fluctuations, contribute to microstructure formation.

*We acknowledge support from the Center for Scientific Computing from the CNSI, MRL: an NSF MRSEC (DMR-1720256) and NSF CNS-1725797. We also thank Asahi Kasei Corp for support.

Presenters

  • Jan Ulric Garcia

    • University of California, Santa Barbara

Authors

  • Jan Ulric Garcia

    • University of California, Santa Barbara
  • Douglas Tree

    • Chemical Engineering Department, Brigham Young Univ - Provo
    • Brigham Young University
    • Brigham Young Univ - Provo
  • Tatsuhiro Iwama

    • Asahi Kasei Corporation
  • Kris T Delaney

    • University of California, Santa Barbara
  • Glenn H Fredrickson

    • University of California, Santa Barbara
    • Chemical Engineering, University of California, Santa Barbara