Three Polyhedron-Based Metal-Organic Frameworks Exhibiting Excellent Acetylene Selective Adsorption

被引:0
|
作者
Zhou, Xia [1 ]
Song, Zitong [1 ]
Krishna, Rajamani [2 ]
Shi, Lixiaoxiao [1 ]
Zhang, Kangli [1 ]
Wang, Dongmei [1 ]
机构
[1] Zhejiang Normal Univ, Coll Chem & Mat Sci, Key Lab Minist Educ Adv Catalysis Mat, Jinhua 321004, Peoples R China
[2] Univ Amsterdam, Vant Hoff Inst Mol Sci, Amsterdam, Netherlands
基金
中国国家自然科学基金;
关键词
metal-organic frameworks; polyhedron-based cage; pore engineering; C2H2; storage; gas adsorption and separation; LEWIS BASIC SITES; HIGH-PERFORMANCE; CARBON-DIOXIDE; SEPARATION; CO2; FUNCTIONALIZATION; PURIFICATION; HYDROCARBONS; CAPACITY; ETHYLENE;
D O I
10.1021/acsami.4c09066
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The separation of acetylene (C2H2) from ethylene (C2H4) and ethane (C2H6) is crucial for the production of high-purity C2H2 and the recovery of other gases. Polyhedron-based metal-organic frameworks (PMOFs) are characterized by their spacious cavities, which facilitate gas trapping, and cage windows with varying sizes that enable gas screening. In this study, we carefully selected a class of PMOFs based on V-type tetracarboxylic acid linker (JLU-Liu22 containing benzene ring, JLU-Liu46 containing urea group and recombinant reconstructed In/Cu CBDA on the basis of JLU-Liu46) to study the relationship between pore environment and C-2 adsorption and separation performance. Among the three compounds, JLU-Liu46 exhibits superior selectivity toward C2H2/C2H4 (2.06) as well as C2H2/C2H6 (2.43). Comparative structural analysis reveals that the exceptional adsorbed-C2H2 performance of JLU-Liu46 can be attributed to the synergistic effects arising from coordinatively unsaturated Cu sites combined with an optimal pore environment (matched pore size and polarity, urea functional group), resulting in a strong affinity between the framework and C2H2 molecules. Furthermore, transient breakthrough simulations of JLU-Liu46 confirmed its potential for separating C2H2 in ternary C-2 gas.
引用
收藏
页码:41542 / 41550
页数:9
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