One Co-MOF with F Active Sites for Separation of C2H2 from CO2, C2H4, and CH4

被引:12
|
作者
Zhang, Xiao-Yu [1 ]
Shi, Wen-Juan [1 ]
Wang, Gang-Ding [1 ]
Hou, Lei [1 ]
Wang, Yao-Yu [1 ]
机构
[1] Northwest Univ, Coll Chem & Mat Sci, Key Lab Synthet & Nat Funct Mol, Shanxi Key Lab Physico Inorgan Chem,Minist Educ, Xian 710127, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORK; ETHANE/ETHYLENE SEPARATION; MIXTURES; ADSORPTION; CRYSTAL; CAPTURE;
D O I
10.1021/acs.inorgchem.3c02486
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Separating acetylene (C2H2) from other light hydrocarbons and carbon dioxide (CO2) mixtures under mild conditions poses significant challenges due to the remarkably similar properties between C2H2 and those gases. For the goal of C2H2 separation, a F-functionalized organic linker, H2F-PyIP = 2-fluorine-5-(4-pyridyl)isophthalic acid, was designed, and the corresponding metal-organic framework (MOF), {[Co-2(F-PyIP)(2)DMF]<middle dot>4H(2)O}(n) (1), was constructed. The MOF with open channels decorated by the active sites of the F groups revealed the exceptional C2H2 uptake and selectivity over CO2, C2H4, and CH4. The breakthrough experiments with different molar ratios of C2H2-C2H4, C2H2-CO2, and other gas mixtures further verified superior separation capacity of the MOF. In particular, the dynamic separation time intervals for gas mixtures (C2H2/CO2 = 1:1, 1:5, 1:10, and 1:20) fell in the range 30-44 min, highlighting the potential of the MOF for tackling the challenging C2H2/CO2 separation process.
引用
收藏
页码:16574 / 16581
页数:8
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