Influence of Pore Morphology on the Diffusion of Water in Triblock Copolymer Membranes

ORAL

Abstract

Understanding the transport properties of water in self-assembled block copolymer morphologies is important for furthering the use of such materials as water-purifying membranes. In this study, we used coarse-grained dissipative-particle-dynamics (DPD) simulations to clarify the influence of pore morphology on the self-diffusion of water in linear-triblock-copolymer membranes. We considered representative lamellar, cylindrical, and gyroid morphologies and present results for both the global and local diffusivities, as well as the structural characteristics of water in the pores. Our results suggest that the diffusivity of water in the confined, polymer-coated pores differs from that in the unconfined bulk. Explicitly, in confinement, the mobility of water is reduced by the hydrodynamic friction arising from the hydrophilic blocks coating the pore walls. We demonstrate that in lamella and cylindrical morphologies, the latter effects can be rendered as a universal function of the pore size relative to the brush height of the hydrophilic blocks.

*Center for Materials for Water and Energy Systems, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences under Award #DE-SC0019272.

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Presenters

  • Venkatraghavan Ganesan

    • University of Texas at Austin

Authors

  • Dipak Aryal

    • University of Texas at Austin

  • Michael Howard

    • Department of Chemical Engineering, Auburn University
    • University of Texas at Austin

  • Rituparna Samanta

    • University of Texas at Austin

  • segolene antoine

    • Chemical Engineering, University of California at Santa Barbara

  • Rachel Segalman

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

  • Thomas M Truskett

    • University of Texas at Austin

  • Venkatraghavan Ganesan

    • University of Texas at Austin