Functionalization of Metal-Organic Frameworks for Enhanced Stability under Humid Carbon Dioxide Capture Conditions

被引:38
|
作者
Andirova, Dinara [1 ]
Lei, Yu [1 ]
Zhao, Xiaodan [1 ]
Choi, Sunho [1 ]
机构
[1] Northeastern Univ, Dept Chem Engn, Snell Engn Ctr 313, Boston, MA 02115 USA
关键词
adsorption; amines; carboxylate ligands; magnesium; metal-organic frameworks; CO2; CAPTURE; MESOPOROUS SILICA; ADSORPTION; ADSORBENTS; STORAGE; SEPARATION; SORBENTS; MCM-36;
D O I
10.1002/cssc.201500580
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal-organic frameworks (MOFs) have been highlighted recently as promising materials for CO2 capture. However, in practical CO2 capture processes, such as capture from flue gas or ambient air, the adsorption properties of MOFs tend to be harmed by the presence of moisture possibly because of the hydrophilic nature of the coordinatively unsaturated sites (CUSs) within their framework. In this work, the CUSs of the MOF framework are functionalized with amine-containing molecules to prevent structural degradation in a humid environment. Specifically, the framework of the magnesium dioxybenzenedicarboxylate (Mg/DOBDC) MOF was functionalized with ethylenediamine (ED) molecules to make the overall structure less hydrophilic. Structural analysis after exposure to high-temperature steam showed that the ED-functionalized Mg/DOBDC (ED-Mg/DOBDC) is more stable under humid conditions, than Mg/DOBDC, which underwent drastic structural changes. ED-Mg/DOBDC recovered its CO2 adsorption capacity and initial adsorption rate quite well as opposed to the original Mg/DOBDC, which revealed a significant reduction in its capture capacity and kinetics. These results suggest that the amine-functionalization of the CUSs is an effective way to enhance the structural stability of MOFs as well as their capture of humid CO2.
引用
收藏
页码:3405 / 3409
页数:5
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