Electrostatically Driven Selective Adsorption of Carbon Dioxide over Acetylene in an Ultramicroporous Material.
Yi XieHui CuiHui WuRui-Biao LinWei ZhouBanglin ChenPublished in: Angewandte Chemie (International ed. in English) (2021)
Separating acetylene from carbon dioxide is important but highly challenging owing to their similar physical properties and molecular dimensions. Herein, we report highly efficient electrostatically driven CO2 /C2 H2 separation in an ultramicroporous cadmium nitroprusside (Cd-NP) with compact pore space and complementary electrostatic potential well fitting for CO2 , thus enabling molecular quadrupole moment recognition of CO2 over C2 H2 . This material shows a high CO2 /C2 H2 uptake ratio of 6.0 as well as remarkable CO2 /C2 H2 selectivity of 85 under ambient conditions with modest CO2 heat of adsorption. Neutron powder diffraction experiments and molecular simulations revealed that the electrostatic potential compatibility between pore structure and CO2 allows it to be trapped in a head-on orientation towards the Cd center, whereas the diffusion of C2 H2 is electrostatically forbidden. Dynamic breakthrough experiments have validated the separation performance of this compound for CO2 /C2 H2 separation.
Keyphrases
- carbon dioxide
- highly efficient
- liquid chromatography
- mass spectrometry
- molecular dynamics simulations
- physical activity
- tandem mass spectrometry
- particulate matter
- aqueous solution
- single molecule
- molecular dynamics
- single cell
- heavy metals
- high performance liquid chromatography
- simultaneous determination
- risk assessment
- nk cells
- ms ms
- optic nerve