Aromatic Amine-Functionalized Covalent Organic Frameworks (COFs) for CO2/N2 Separation.

Abstract

CO2 is a prominent example for an exhaust gas, and it is known for its high impact on global warming. Therefore, carbon capture from CO2 emissions of industrial processes is increasingly important to halt and prevent the disruptive consequences of global warming. Covalent organic frameworks (COFs) as porous nanomaterials have been shown to selectively adsorb CO2 in high quantities and with high CO2/N2 selectivity. Interactions with amines are recognized to selectively adsorb CO2 and help capture it from exhaust emissions. Herein, a novel COF (Me3TFB-(NH2)2BD), which was not accessible via a direct condensation reaction, was synthetized by dynamic linker exchange starting with Me3TFB-BD. Despite the linker exchange, the porosity of the COF was largely maintained, resulting in a high BET surface area of 1624 ± 89 m2/g. The CO2 and N2 adsorption isotherms at 273 and 295 K were studied to determine the performance in carbon capture at flue gas conditions. Me3TFB-(NH2)2BD adsorbs 1.12 ± 0.26 and 0.72 ± 0.07 mmol/g of CO2 at 1 bar and 273 and 295 K, respectively. The COF shows a high CO2/N2 IAST selectivity under flue gas conditions (273 K:83 ± 11, 295 K: 47 ± 11). The interaction of the aromatic amine groups with CO2 is based on physisorption, which is expected to make the regeneration of the material energy efficient.