4.7 Article

Reactive Molecular Dynamics Study of Hygrothermal Degradation of Crosslinked Epoxy Polymers

期刊

ACS APPLIED POLYMER MATERIALS
卷 4, 期 6, 页码 4411-4423

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsapm.2c00383

关键词

hygrothermal degradation; reactive molecular dynamics; ReaxFF; epoxy-amine network; polymers; water absorption

资金

  1. United States Navy's Office of Naval Research [N00014-22-1-2129]
  2. National Science Foundation (NSF) under NSF CMMI [2113558]
  3. NSF MRI award [OAC-2019077]
  4. ND EPSCoR award [IIA-1355466]
  5. State of North Dakota
  6. Extreme Science and Engineering Discovery Environment (XSEDE) [TG-DMR110088]
  7. Directorate For Engineering
  8. Div Of Civil, Mechanical, & Manufact Inn [2113558] Funding Source: National Science Foundation

向作者/读者索取更多资源

This study presents a reactive molecular dynamics simulation framework to investigate the hygrothermal aging process of epoxy thermosets. The simulations reveal the interaction between water molecules and the epoxy network, shedding light on the degradation mechanisms and providing insights for improving the durability and performance of epoxy thermosets in humid environments.
Epoxy thermosets are often exposed to high humidity environments in various applications, undergoing reversible and irreversible degradation depending on the environment. This study presents a reactive molecular dynamics (MD) simulation framework to gain deeper insights into the hygrothermal aging process, which is essential to develop a targeted approach to combat water-assisted degradation in epoxy thermosets. By applying ReaxFF potential, an epoxy-amine network is created at low temperatures to avoid unwanted hightemperature side reactions, where the water molecules are added to achieve the desired degree of moisture contamination. The simulations show that in addition to the plasticization effect from the moisture ingress, the epoxy network shows recovery in mechanical properties and density due to the multi-site interaction of the water molecule with the electronegative sites within the network. Moreover, long-term exposure to humidity or direct exposure due to cracking can induce irreversible changes in the epoxy-amine network. The protonation of the water molecule and nucleophilic attack on the C-O bond of the ether linkages in the epoxy-amine networks are successfully simulated by applying reactive MD simulations. Remarkably, the simulations show that the selectivity of water molecules for the hydrolysis reaction in the epoxy network depends on the spatial arrangement and the steric hindrance of the network. This work provides molecular level insights into hygrothermal aging by elucidating the interplay between free volume and polarity of the network in the physical aging of the moist epoxy networks, paving a way for advanced design strategy toward better durability and performance of epoxy thermosets in humid environments.

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