Activation-Controlled Structural Integrity in A520 MOF Membranes for Efficient CO2/N2 and CO2/CH4 Separation
Journal
ACS Applied Materials and Interfaces
Journal Volume
18
Journal Issue
28
Start Page
38960
End Page
38971
ISSN
1944-8244
1944-8252
Date Issued
2026-07-08
Author(s)
Abstract
Aluminum fumarate (A520) is a promising metal–organic framework (MOF) for gas adsorption and separation. However, the fabrication of dense, pristine polycrystalline A520 membranes has not yet been reported. Herein, we present a robust seeded-growth protocol to fabricate continuous A520 polycrystalline membranes with a thickness of approximately 3 μm on α-alumina substrates. Our results demonstrate that the post-synthetic activation process plays a critical role in determining membrane integrity. In particular, a methanol exchange (ME) pretreatment prior to thermal activation effectively suppresses lattice distortion induced by capillary stress during solvent evaporation, as evidenced by X-ray diffraction and gas permeation tests. The resulting A520 (ME) membranes exhibit excellent molecular sieving performance, with ideal CO2/N2 and CO2/CH4 selectivities of 71 and 112, respectively. Mixed-gas permeation measurements reveal pronounced composition-dependent separation behavior, where the CO2/N2 separation factor reaches 153 at a 20 mol % CO2 feed, exceeding the 2019 Robeson upper bound, but decreases at higher CO2 concentrations. This behavior is associated with composition-dependent competitive adsorption and diffusion within the confined A520 channels. Grand canonical Monte Carlo (GCMC) simulations reveal that increasing N2 partial pressure enhances N2 uptake but significantly reduces its diffusional mobility, suggesting that additional N2 molecules occupy less favorable transport environments and experience increased diffusion resistance. In contrast, CO2/CH4 separation remains primarily governed by the intrinsic molecular sieving capability of the A520 framework, where the larger kinetic diameter of CH4 results in stronger diffusion limitation. These results highlight the importance of controlled activation strategies and provide insights into the interplay between competitive adsorption and confined diffusion in A520 membranes for carbon capture applications.
Subjects
A520
CO2capture
CO2separation
membrane gas separation
metal−organic framework
MOF membrane
Publisher
American Chemical Society (ACS)
Type
journal article