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A series of new nitrogen-rich aminal-linked porous organic polymers (APOPs) has been constructed by cost-effective and simple condensation reactions between diaminotriazine-based tectonics and benzaldehyde. The facile and one-pot approach suggests a platform to incorporate functional groups in their pores to tune the affinity between gas molecules and the frameworks. Due to the chemical functionalization and nitrogen-rich pore surface, the APOPs with a moderate specific surface area (SBET = 724–1402 m2 g−1) exhibit significant gas adsorption and high isosteric heats of adsorption (CO2: up to 4.54 mmol g−1 at 273 K and 1 bar, 33.3 kJ mol−1; H2: up to 8.95 mmol g−1 at 77 K and 1 bar, 9.4 kJ mol−1). The isosteric heats of adsorption (Qst) can be tuned by the selection of polar group functionalized building blocks, and their values can be enhanced from 26.6 to 33.3 kJ mol−1 for CO2, while the increasing of Qst is beneficial for flue gas separation. Indeed, the strong affinity for CO2 within the APOPs gives rise to a higher CO2 uptake at low pressures (0.15 bar) along with good selectivity over N2.
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Song et al. (2013) studied this question.
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