Enhancing Selective Hydrofluorocarbon Greenhouse Gas Capture via Halogenation of Metal-Organic Frameworks

被引:1
|
作者
Jerozal, Ronald T. [1 ,2 ]
Kim, Jaehwan [1 ,3 ]
Ma, Carolyn [1 ]
Pitt, Tristan A. [1 ]
Lee, Jung-Hoon [4 ,5 ]
Milner, Phillip J. [1 ]
机构
[1] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14850 USA
[2] Hamilton Coll, Dept Chem, Clinton, NY 13323 USA
[3] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[4] Korea Inst Sci & Technol KIST, Computat Sci Res Ctr, Seoul 02792, South Korea
[5] Korea Univ, KU KIST Grad Sch Converging Sci & Technol, Seoul 02841, South Korea
基金
新加坡国家研究基金会; 美国国家科学基金会;
关键词
ADSORPTION; TRIFLUOROMETHANE; ZEOLITES; SEPARATION; SORPTION; UIO-66; CHEMISTRY; REAGENTS; CHF3;
D O I
10.1021/jacs.5c00393
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrofluorocarbons (HFCs) are anthropogenically produced greenhouse gases with longer atmospheric lifetimes and higher global warming potentials than those of carbon dioxide. General strategies to abate their emissions from industrial point sources, such as via adsorptive capture, remain scarce. Herein, we uncover the key structure-property relationships that lead to strong binding of HFCs such as fluoroform (CHF3) and difluoromethane (CH2F2) in metal-organic frameworks (MOFs) under the low pressures relevant to flue gas scrubbing. Extensive gas sorption and computational studies support that the Zr-based microporous framework MOF-801-Br or HHU-2-Br (HHU = Heinrich-Heine-University Dusseldorf) strongly binds HFCs due to its synergistic combination of Zr-OH sites on the nodes and bromine sites on the linkers. As such, MOF-801-Br demonstrates a record-setting performance for separating CHF3 from N2 under dilute conditions. Our work highlights that the combination of multiple hydrogen-bonding sites in microporous MOFs represents a generalizable strategy for HFC capture, enabling their selective removal from industrial waste streams.
引用
收藏
页码:7127 / 7136
页数:10
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