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Pore Space Partition within a Metal–Organic Framework for Highly Efficient C₂H₂/CO₂ Separation

Author:
Ye, Yingxiang, Ma, Zhenlin, Lin, Rui-Biao, Krishna, Rajamani, Zhou, Wei, Lin, Quanjie, Zhang, Zhangjing, Xiang, Shengchang, Chen, Banglin
Source:
Journal of the American Chemical Society 2019 v.141 no.9 pp. 4130-4136
ISSN:
1520-5126
Subject:
acetylene, carbon dioxide, coordination polymers, ligands, molecular models, pyridines
Abstract:
The pore space partition (PSP) approach has been employed to realize a novel porous MOF (FJU-90) with dual functionalities for the challenging C₂H₂/CO₂ separation under ambient conditions. By virtue of a triangular ligand (Tripp = 2,4,6-tris(4-pyridyl)pyridine), the cylindrical channels in the original FJU-88 have been partitioned into uniformly interconnected pore cavities, leading to the dramatically reduced pore apertures from 12.0 × 9.4 to 5.4 × 5.1 Ų. Narrowing down the pore sizes, the resulting activated FJU-90a takes up a very large amount of C₂H₂ (180 cm³ g–¹) but much less of CO₂ (103 cm³ g–¹) at 298 K and 1 bar, demonstrating it to be the best porous MOF material for this C₂H₂/CO₂ (50%:50%) separation in terms of the C₂H₂ gravimetric productivity. IAST calculations, molecular modeling studies, and simulated and experimental breakthrough experiments comprehensively demonstrate that the pore space partition strategy is a very powerful approach to constructing MOFs with dual functionality for challenging gas separation.
Agid:
6323994