Metal-Organic Frameworks Possessing Suitable Pores for Xe/Kr Separation

被引:3
|
作者
Zeng, Dong-Mei [1 ]
Huang, Lian [1 ]
Fu, Xing-Ping [2 ]
Wang, Yu-Ling [1 ]
Chen, Junmin [1 ]
Liu, Qing-Yan [1 ,2 ]
机构
[1] Jiangxi Normal Univ, Coll Chem & Chem Engn, Natl Engn Res Ctr Carbohydrate Synth, Nanchang 330022, Jiangxi, Peoples R China
[2] Wuyi Univ, Coll Ecol & Resources Engn, Fujian Prov Key Lab Ecoind Green Technol, Wuyi 354300, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
XENON; ADSORPTION; GAS; PROTEINS; INSIGHTS; BINDING; SITES; MOF;
D O I
10.1021/acs.inorgchem.4c00122
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Adsorption separation of the Xe/Kr mixture remains a tough issue since Xe and Kr have an inert nature and similar sizes. Here we present a chlorinated metal-organic framework (MOF) [JXNU-19(Cl)] and its nonchlorinated analogue (JXNU-19) for Xe/Kr separation. The two isostructural MOFs constructed from the heptanuclear cobalt-hydroxyl clusters bridged by organic ligands are three-dimensional structures. Detailed contrast of the Xe/Kr adsorption separation properties of the MOF shows that significantly enhanced Xe uptakes and Xe/Kr adsorption selectivity (17.1) are observed for JXNU-19 as compared to JXNU-19(Cl). The main binding sites for Xe in the MOF revealed by computational simulations are far away from the chlorine sites, suggesting that the introduction of the chlorine groups results in the unfavorable Xe adsorption for JXNU-19(Cl). The optimal pores, high surface area, and multiple strong Xe-framework interactions facilitate the effective Xe/Kr separation for JXNU-19.
引用
收藏
页码:5151 / 5157
页数:7
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