A Microporous Metal-Organic Framework Supramolecularly Assembled from a CuII Dodecaborate Cluster Complex for Selective Gas Separation

被引:244
作者
Zhang, Yuanbin [1 ]
Yang, Lifeng [1 ]
Wang, Lingyao [2 ]
Duttwyler, Simon [2 ]
Xing, Huabin [1 ]
机构
[1] Zhejiang Univ, Coll Chem & Biol Engn, Key Lab Biomass Chem Engn, Minist Educ, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ, Dept Chem, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国博士后科学基金;
关键词
adsorption; dedecaborate; gas separation; metal-organic frameworks; porous materials; LIGHT-HYDROCARBONS; CLOSO-DODECABORATE; COORDINATION POLYMER; CO2; UPTAKE; ADSORPTION; SORPTION; METHANE; DESIGN; ANIONS;
D O I
10.1002/anie.201903600
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel 3D metal-organic framework BSF-1 based on the closo-dodecaborate cluster [B12H12](2-) was readily prepared at room temperature by supramolecular assembly of CuB12H12 and 1,2-bis(4-pyridyl)acetylene. The permanent microporous structure was studied by X-ray crystallography, powder X-ray diffraction, IR spectroscopy, thermogravimetric analysis, and gas sorption. The experimental and theoretical study of the gas sorption behavior of BSF-1 for N-2, C2H2, C2H4, CO2, C3H8, C2H6, and CH4 indicated excellent separation selectivities for C3H8/CH4, C2H6/CH4, and C2H2/CH4 as well as moderately high separation selectivities for C2H2/C2H4, C2H2/CO2, and CO2/CH4. Moreover, the practical separation performance of C3H8/CH4 and C2H6/CH4 was confirmed by dynamic breakthrough experiments. The good cyclability and high water/thermal stability render it suitable for real industrial applications.
引用
收藏
页码:8145 / 8150
页数:6
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