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A porous organic polymer named FC-POP was facilely synthesized with extraordinary porosity and excellent stability. Further covalent incorporation of various amines including single amine group, multi-amine groups of diethylenediamine (DETA), and poly-amine groups of polyethylenimine (PEI) to the network gave rise to task-specific modification of the microenvironments to make them more suitable for CO 2 capture. As a result, significant boost of CO 2 adsorption capacity of 4.5 mmol/g (for FC-POP–CH 2 DETA, 273 K, 1 bar) and the CO 2 /N 2 selectivity of 736.1 (for FC-POP–CH 2 PEI) were observed after the post-synthesis amine modifications. Furthermore, these materials can be regenerated in elevated temperature under vacuum without apparent loss of CO 2 adsorption capacity.
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Li et al. (2016) studied this question.
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