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Ion and Water Dynamics in the Transition from Dry to Wet Conditions in Salt-Doped PEG.
Marioni, Nico; Nordness, Oscar; Zhang, Zidan; Sujanani, Rahul; Freeman, Benny D; Segalman, Rachel A; Clément, Raphaële J; Ganesan, Venkat.
Affiliation
  • Marioni N; McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.
  • Nordness O; Department of Chemical Engineering, University of California Santa Barbara, Santa Barbara, California 93106, United States.
  • Zhang Z; McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.
  • Sujanani R; Materials Department and Materials Research Laboratory, University of California Santa Barbara, Santa Barbara, California 93106, United States.
  • Freeman BD; Department of Chemical Engineering, University of California Santa Barbara, Santa Barbara, California 93106, United States.
  • Segalman RA; McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.
  • Clément RJ; Materials Department and Materials Research Laboratory, University of California Santa Barbara, Santa Barbara, California 93106, United States.
  • Ganesan V; Department of Chemical Engineering, University of California Santa Barbara, Santa Barbara, California 93106, United States.
ACS Macro Lett ; 13(3): 341-347, 2024 Mar 19.
Article in En | MEDLINE | ID: mdl-38428022
ABSTRACT
The influence of the water content on ion and water transport mechanisms in polymer membranes under low to moderate hydration conditions remains poorly understood. In this study, we combine ion and water diffusivity (PFG-NMR) measurements with atomistic molecular dynamics simulations to better understand transport processes in hydrated salt-doped poly(ethylene glycol). Above the water percolation threshold, the experimental and simulated diffusivities are in good agreement with the free volume transport models. At low hydration levels, unlike dry systems, ion diffusion cannot be described by polymer segmental dynamics alone. We rationalize such observations by the interplay between ion-water and ion-polymer solvation of cations and between ion-water and cation-anion interactions for anions. Further, we demonstrate that a two-state model combining ion-water solvation and free volume transport can describe water dynamics across the entire hydration range of interest. Our findings provide a more encompassing analysis of ion and water transport in hydrated polyelectrolytes, specifically in the low hydration regime.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: ACS Macro Lett Year: 2024 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: ACS Macro Lett Year: 2024 Document type: Article Affiliation country: United States
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