Pore Space Partition within a Metal–Organic Framework for Highly Efficient C2H2/CO2 Separation
| Authors |
|
|---|---|
| Publication date | 06-03-2019 |
| Journal | Journal of the American Chemical Society |
| Volume | Issue number | 141 | 9 |
| Pages (from-to) | 4130-4136 |
| Number of pages | 7 |
| Organisations |
|
| 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 Å2. 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.
|
| Document type | Article |
| Note | With supplementary files |
| Language | English |
| Related dataset | CCDC 1882901: Experimental Crystal Structure Determination |
| Published at | https://doi.org/10.1021/jacs.9b00232 |
| Permalink to this page | |