Relationship between microporous structure and light gas transport through glassy polymeric membranes revealed by molecular simulations

Journal Article · Fri Jul 04 00:00:00 EDT 2025 · Journal of Materials Chemistry. A

DOI:https://doi.org/10.1039/D5TA02906F· OSTI ID:2947440

Bao Le, Tran Thi ^[1]; Condes, Lucas C. ^[1]; Barbosa, Gabriel D. ^[1]; Perez, Felipe ^[1]; Webb, Matthew T. ^[1]; Galizia, Michele ^[1]; Nardelli, Marco Buongiorno ^[2]; Striolo, Alberto ^[1]

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1. Univ. of Oklahoma, Norman, OK (United States)
2. Univ. of North Texas, Denton, TX (United States)

Microporous glassy polymers are attractive materials for gas separation membranes, due to their high permeability and tailorable selectivity, provided physical aging can be delayed. The archetypal microporous glassy polymer, PTMSP, can be blended with a hyper-crosslinked isatin–triptycene porous polymer network (PPN) to delay physical aging. However, while PPN is effective at reducing physical aging, it also affects the permeability of light gases through PTMSP. Molecular dynamics simulations were used here to shed fundamental light on the mechanisms responsible for these effects. Atomistic models are developed that satisfactorily reproduce experimental observations such as matrix density and cavity size distributions for neat PTMSP as well as for PTMSP–PPN blends. Analysis of the simulation results suggests that physical aging is delayed because the PPN inclusions slow down PTMSP relaxation while reducing the connectivity between free volume pockets. To understand how PPN inclusions affect light gas permeability, the atomistic models developed are used to probe CO₂ and CH₄ diffusion and sorption. These simulations are conducted for PTMSP matrices exhibiting varying density, towards reproducing experimental permeability data. Interrogating the simulation trajectories, it is discovered that while CH₄ travels preferentially through the free volume cavities, CO₂ preferentially interacts with the available surfaces, especially in the presence of PPN. These differences help interpret experimental observations. The transport of C₂H₆ and H₂S through PTMSP matrices was also investigated. These gases, and in particular H₂S, were found to absorb within PTMSP, yielding very low diffusion coefficients. The ability to predict differences in diffusion pathways for various natural gas components unveils the possibility of engineering membranes to control permeability and selectivity towards large-scale applications.

• Research Organization: Univ. of Oklahoma, Norman, OK (United States)
• Sponsoring Organization: USDOE Office of Science (SC), Basic Energy Sciences (BES). Chemical Sciences, Geosciences & Biosciences Division (CSGB)
• Grant/Contract Number: SC0024554
• OSTI ID: 2947440
• Journal Information: Journal of Materials Chemistry. A, Journal Name: Journal of Materials Chemistry. A Journal Issue: 34 Vol. 13; ISSN 2050-7488; ISSN 2050-7496
• Publisher: Royal Society of Chemistry
• Country of Publication: United States
• Language: English