Microporous Metal-Organic Framework with Dual Functionalities for Efficient Separation of Acetylene from Light Hydrocarbon Mixtures

被引:83
作者
Li, Hao [1 ,2 ]
Li, Libo [2 ,3 ]
Lin, Rui-Biao [2 ]
Ramirez, Giorgio [2 ]
Zhou, Wei [4 ]
Krishna, Rajamani [5 ]
Zhang, Zhangjing [1 ]
Xiang, Shengchang [1 ]
Chen, Banglin [2 ]
机构
[1] Fujian Normal Univ, Fujian Prov Key Lab Polymer Mat, Coll Mat Sci & Engn, Fuzhou 350007, Fujian, Peoples R China
[2] Univ Texas San Antonio, Dept Chem, 1 UTSA Circle, San Antonio, TX 78249 USA
[3] Taiyuan Univ Technol, Coll Chem & Chem Engn, Taiyuan 030024, Shanxi, Peoples R China
[4] NIST, NIST Ctr Neutron Res, Gaithersburg, MD 20899 USA
[5] Univ Amsterdam, Vant Hoff Inst Mol Sci, Sci Pk 904, NL-1098 XH Amsterdam, Netherlands
基金
中国国家自然科学基金;
关键词
Metal-organic frameworks; Light hydrocarbons; Gas separation; Acetylene; ADSORPTION; CO2; CHEMISTRY; ETHYLENE; REMOVAL;
D O I
10.1021/acssuschemeng.8b05480
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Separating acetylene from light hydrocarbon mixtures like ethylene is a very important process for downstream industrial applications. Herein, we report a new MOF [CuL2(SiF6)] (UTSA-220, L = (1E,2E)-1,2-bis(pyridin-4-ylmethylene)hydrazine) with dual functionalities featuring optimal pore size with strong binding sites for acetylene. UTSA-220 exhibits apparently higher uptake capacity for C2H2 than those for other light hydrocarbons. The potential of this material for trace C2H2 removal from C2H4 has also been demonstrated by a dynamic breakthrough experiment performed with C2H2/C2H4 (1/99 v/v) under simulated industrial conditions. According to the dispersion-corrected density functional theory (DFT-D) simulation, SiF62- and azine moieties serve as preferential binding sites for C2H2, indicating the feasibility of the dual functionalities incorporated in UTSA-220 for adsorbent-based C2H2 separations.
引用
收藏
页码:4897 / 4902
页数:11
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