4.7 Article

Mechanisms of Asymmetric Membrane Formation in Nonsolvent-Induced Phase Separation

Journal

ACS MACRO LETTERS
Volume 9, Issue 11, Pages 1617-1624

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsmacrolett.0c00609

Keywords

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Funding

  1. Asahi Kasei Corporation
  2. Center for Materials for Water and Energy Systems (MWET), an Energy Frontier Research Center - U.S. Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0019272]
  3. Brigham Young University
  4. MRL: a National Science Foundation (NSF) Materials Research Science and Engineering Center (MRSEC) [DMR-1720256]
  5. NSF [CNS-1725797]
  6. Natural Sciences and Engineering Research Council of Canada (NSERC) PGS-D scholarship program

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We report the first simulations of nonsolvent-induced phase separation (NIPS) that predict membrane microstructures with graded asymmetric pore size distribution. In NIPS, a polymer solution film is immersed in a nonsolvent bath, enriching the film in nonsolvent, and leading to phase separation that forms a solid polymer-rich membrane matrix and polymer-poor membrane pores. We demonstrate how mass-transfer-induced spinodal decomposition, thermal fluctuations, and glass-transition dynamics-implemented with mobility contrast between the polymer-rich and polymer-poor phases-are essential to the formation of asymmetric membrane microstructures. Specifically, we show that the competition between the propagation of the phase-separation and glass-transition fronts determines the degree of pore-size asymmetry. We also explore the sensitivity of these microstructures to the initial film composition, and compare their formation in 2D and 3D.

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