4.7 Article

Subdiffusive High-Pressure Hydrogen Gas Dynamics in Elastomers

Journal

MACROMOLECULES
Volume 55, Issue 10, Pages 3788-3800

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.2c00204

Keywords

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Funding

  1. U.S. Department of Energy (USDOE), Office of Energy Efficiency and Renewable Energy (EERE), Hydrogen and Fuel Cell Technologies Office (HFTO) [DE-AC05-76RL01830]
  2. U.S. Department of Energy's National Nuclear Security Administration [DE-NA0003525]

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This study investigates the diffusion behavior of hydrogen gas in EPDM using molecular dynamics simulations, revealing anomalous subdiffusive motion at high pressure and intermediate times. Increasing cross-link density at lower temperatures reduces hydrogen gas localization and cavitation precursors.
Elastomeric rubber materials serve a vital role as sealing materials in the hydrogen storage and transport infrastructure. With applications including O-rings and hose liners, these components are exposed to pressurized hydrogen at a range of temperatures, cycling rates, and pressure extremes. Highpressure exposure and subsequent rapid decompression often lead to cavitation and stress-induced damage of the elastomer due to localization of the hydrogen gas. Here, we use all-atom classical molecular dynamics simulations to assess the impact of compositional variations on gas diffusion within the commonly used elastomer ethylene-propylene-diene monomer (EPDM). With the aim to build a predictive understanding of precursors to cavitation and to motivate material formulations that are less sensitive to hydrogen-induced failure, we perform systematic simulations of gas dynamics in EPDM as a function of temperature, gas concentration, and cross-link density. Our simulations reveal anomalous, subdiffusive hydrogen motion at pressure and intermediate times. We identify two groups of gas with different mobilities: one group exhibiting high mobility and one group exhibiting low mobility due to their motion being impeded by the polymer. With decreasing temperatures, the low-mobility group shows increased gas localization, the necessary precursor for cavitation damage in these materials. At lower temperatures, increasing cross-link density led to greater hydrogen gas mobility and a lower fraction of caged hydrogen, indicating that increasing cross-link density may reduce precursors to cavitation. Finally, we use a two-state kinetic model to determine the energetics associated with transitions between these two mobility states.

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