微型多孔材料
吸附
钴
金属有机骨架
化学
选择性
分子
金属
气体分离
巴(单位)
二甲基乙酰胺
选择性吸附
无机化学
物理化学
催化作用
有机化学
膜
溶剂
物理
气象学
生物化学
作者
Liang Qin,Yan Li,Fenglan Liang,Lijun Li,Yuwen Lan,Zhiyong Li,Xiaoting Lu,Manqi Yang,De‐Yun Ma
标识
DOI:10.1016/j.micromeso.2022.112098
摘要
A new microporous 2D Co-based MOF, [Co3(C6H3NO2)2(cpna)2(DMA)2]n (1) (H2cpna = 6-(4-carboxylphenyl)nicotinic acid; DMA = N,N-dimethylacetamide), has been synthesized and structurally characterized. Complex 1 shows a 2D network with 1D channel of 6.4 × 9.3 Å2 along the a-axis. Activated 1 (1a) exhibits selective gas adsorption for CO2 as compared to other gas molecules (e.g. C2H2, CH4, CO, N2) from the experimental single-component gas-adsorption isotherm (at 273K and 298K), molecular simulation and breakthrough experiments (298K). And the adsorption selectivity (CO2/C2H2, CO2/CH4, CO2/CO, and CO2/N2) was calculated with the ideal adsorbed solution theory (IAST). Activated 1 shows 9.77 wt% (2.22 mmol/g) uptake of CO2 at 1 bar and 273 K. Furthermore, the activation of 1 exhibits high ideal selectivities in adsorption of CO2 over C2H2, CH4, CO, and N2 at 298 K (1 bar), which may be attributed to the pyridyl sites on the ligands and open metal sites on the nodes of the framework. Besides, 1a could adsorb more gas molecules due to thicker layer (10.97 Å) of 2D structure.
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