Abstract
Poly(1,3-dioxolane) has emerged as a leading membrane material for post-combustion CO2 capture due to its high ether oxygen content and strong affinity toward CO2. However, they are often cross-linked to inhibit crystallization, which makes them impossible to fabricate into industrial thin-film composite membranes. Herein, soluble and high molecular weight bottlebrush polymers (bPDXLA) are synthesized using reversible addition-fragmentation chain transfer polymerization and demonstrate the feasibility of fabricating nanofilm (≈100 nm) composite membranes (NCMs). Furthermore, bPDXLA can be plasticized using a miscible additive of poly(ethylene glycol) dimethyl ether (PEGDME) to improve CO2 permeability while retaining good CO2/N2 selectivity. For example, adding 20 mass% PEGDME improves CO2 permeance from 930 to 1300 GPU and decreases CO2/N2 selectivity from 74 to 53 at 25 °C; the membrane exhibits stable separation performance competitive with state-of-the-art commercial membranes. This work unveils a practical approach to designing uncross-linked, highly polar polymers for practical membrane gas separation and highlights a facile way to enhance performance by incorporating miscible plasticizers using industrial manufacturing processes.
| Original language | English |
|---|---|
| Article number | 2503461 |
| Journal | Small |
| Volume | 21 |
| Issue number | 25 |
| DOIs | |
| State | Published - Jun 26 2025 |
Keywords
- CO/N separation
- bottlebrush polymers
- nanofilm composite membranes
- poly(1,3-dioxolane)
- poly(ethylene glycol) dimethyl ether
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