Separation of Aromatic Hydrocarbons in Porous Materials

被引:94
作者
Idrees, Karam B. [1 ]
Li, Zhao [2 ]
Xie, Haomiao [1 ]
Kirlikovali, Kent O. [1 ]
Kazem-Rostami, Masoud [1 ]
Wang, Xingjie [1 ]
Wang, Xijun [2 ]
Tai, Tzu-Yi [1 ]
Islamoglu, Timur [1 ]
Stoddart, J. Fraser [1 ,3 ,4 ,5 ]
Snurr, Randall Q. [2 ]
Farha, Omar K. [1 ,2 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
[3] Zhejiang Univ, Stoddart Inst Mol Sci, Dept Chem, Hangzhou 310021, Peoples R China
[4] ZJU, Hangzhou Global Sci & Technol Innovat Ctr, Hangzhou 311215, Peoples R China
[5] Univ New South Wales, Sch Chem, Sydney, NSW 2052, Australia
关键词
metal; organic frameworks; separation; xylenes; fl exibility; XYLENE ISOMERS; SELECTIVITY; ADSORPTION; SORPTION; MOF;
D O I
10.1021/jacs.2c03114
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
ABSTRACT: Industrial-scale thermal separation processes have contributed greatly to the rise in carbon dioxide emissions. Porous materials, such as metal-organic frameworks (MOFs), can potentially reduce these emissions by achieving nonthermal chemical separations through the physical adsorption of targeted species with high selectivity. Here, we report the synthesis of the channel-based MOFs NU-2000 and NU-2001, which are constructed from threedimensional (3D) linkers, to separate the industrially relevant xylene isomers under ambient conditions by leveraging sub-angstrom ngstrom differences in the sizes of each isomer. While the rotation of twodimensional (2D) linkers in MOFs often affords changes in pore apertures and pore sizes that are substantial enough to hinder separation efficiency, increasing the linker dimensionality from 2D to three-dimensional (3D) enables precise control of the MOF pore size and aperture regardless of the linker orientation, establishing this design principle as a broadly applicable strategy.
引用
收藏
页码:12212 / 12218
页数:7
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