Adsorption Site Selective Occupation Strategy within a Metal-Organic Framework for Highly Efficient Sieving Acetylene from Carbon Dioxide

被引:117
|
作者
Yang, Lingzhi [1 ]
Yan, Liting [2 ]
Wang, Ying [3 ]
Liu, Zhi [1 ]
He, Jiangxiu [1 ]
Fu, Qiuju [1 ]
Liu, Dandan [4 ]
Gu, Xin [4 ]
Dai, Pengcheng [4 ]
Li, Liangjun [4 ]
Zhao, Xuebo [1 ,2 ]
机构
[1] China Univ Petr East China, State Key Lab Heavy Oil Proc, Coll Chem Engn, Qingdao 266580, Peoples R China
[2] Qilu Univ Technol, Shandong Acad Sci, Key Lab Proc & Testing Technol Glass & Funct Cera, Sch Mat Sci & Engn, Jinan 250353, Peoples R China
[3] Shaanxi Normal Univ, Key Lab Macromol Sci Shaanxi Prov, Key Lab Appl Surface & Colloid Chem, Minist Educ,Sch Chem & Chem Engn, Xian 710062, Shaanxi, Peoples R China
[4] China Univ Petr East China, Inst New Energy, Qingdao 266580, Peoples R China
关键词
acetylene; adsorption site-selective occupation; amino functional groups; carbon dioxide; metal– organic frameworks; SEPARATION; CO2; C2H2/CO2; BINDING; STORAGE; ETHYLENE;
D O I
10.1002/anie.202013965
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The separation of acetylene and carbon dioxide is an essential but challenging process owing to the similar molecular sizes and physical properties of the two gas molecules. Notably, these molecules usually exhibit different orientations in the pore channel. We report an adsorption site selective occupation strategy by taking advantage of differences in orientation to sieve the C2H2 from CO2 in a judiciously designed amine-functionalized metal-organic framework, termed CPL-1-NH2. In this material, the incorporation of amino groups not only occupies the adsorption sites of CO2 molecules and shields the interaction of uncoordinated oxygen atom and CO2 molecules resulting in a negligible adsorption amount and a decrease in enthalpy of adsorption but also strengthened the binding affinity toward C2H2 molecules. This material thus shows an extremely high amount of C2H2 at low pressure and a remarkably high C2H2/CO2 IAST selectivity (119) at 1 bar and 298 K.
引用
收藏
页码:4570 / 4574
页数:5
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