离子液体
双氰胺
复合数
密度泛函理论
选择性
金属有机骨架
巴(单位)
吸附
材料科学
化学工程
分子
气体分离
烟气
离子键合
化学
无机化学
物理化学
复合材料
计算化学
有机化学
催化作用
离子
物理
气象学
膜
生物化学
工程类
作者
Nitasha Habib,Özce Durak,Hasan Can Gülbalkan,Ayça Aydoğdu,Seda Keskın,Alper Uzun
标识
DOI:10.1021/acsaenm.3c00010
摘要
Capturing CO2 selectively from flue gas and natural gas addresses the criteria of a sustainable society. In this work, we incorporated an ionic liquid (IL) (1-methyl-1-propyl pyrrolidinium dicyanamide, [MPPyr][DCA]) into a metal organic framework (MOF), MIL-101(Cr), by wet impregnation and characterized the resulting [MPPyr][DCA]/MIL-101(Cr) composite in deep detail to identify the interactions between [MPPyr][DCA] molecules and MIL-101(Cr). Consequences of these interactions on the CO2/N2, CO2/CH4, and CH4/N2 separation performance of the composite were examined by volumetric gas adsorption measurements complemented by the density functional theory (DFT) calculations. Results showed that the composite offers remarkably high CO2/N2 and CH4/N2 selectivities of 19,180 and 1915 at 0.1 bar and 15 °C corresponding to 1144- and 510-times improvements, respectively, as compared to the corresponding selectivities of pristine MIL-101(Cr). At low pressures, these selectivities reached practically infinity, making the composite completely CO2-selective over CH4 and N2. The CO2/CH4 selectivity was improved from 4.6 to 11.7 at 15 °C and 0.001 bar, yielding a 2.5-times improvement, attributed to the high affinity of [MPPyr][DCA] toward CO2, validated by the DFT calculations. These results offer broad opportunities for the design of composites where ILs are incorporated into the pores of MOFs for high performance gas separation applications to address the environmental challenges.
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