化学
烟气
吸附
吸附
金属有机骨架
二氧化碳
胺气处理
无机化学
碳酸氢盐
化学工程
有机化学
工程类
作者
Hao Lyu,Oscar Iu‐Fan Chen,Nikita Hanikel,Mohammad I. Hossain,Robinson W. Flaig,Xiaokun Pei,Ameer Amin,Mark D. Doherty,Rebekah K. Impastato,T. Grant Glover,David R. Moore,Omar M. Yaghi
摘要
Metal–organic framework-808 has been functionalized with 11 amino acids (AA) to produce a series of MOF-808-AA structures. The adsorption of CO 2 under flue gas conditions revealed that glycine- and dl -lysine-functionalized MOF-808 (MOF-808-Gly and - dl -Lys) have the highest uptake capacities. Enhanced CO 2 capture performance in the presence of water was observed and studied by using single-component sorption isotherms, CO 2 /H 2 O binary isotherm, and dynamic breakthrough measurements. The key to the favorable performance was uncovered by deciphering the mechanism of CO 2 capture in the pores and attributed to the formation of bicarbonate as evidenced by 13 C and 15 N solid-state nuclear magnetic resonance spectroscopy studies. On the basis of these results, we examined the performance of MOF-808-Gly in simulated coal flue gas conditions and found that it is possible to capture and release CO 2 by vacuum swing adsorption. MOF-808-Gly was cycled at least 80 times with full retention of performance. This study significantly advances our understanding of CO 2 chemistry in MOFs by revealing how strongly bound amine moieties to the MOF backbone create the chemistry and environment within the pores, leading to the binding and release of CO 2 under mild conditions without application of heat.
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