Abstract
Novel preferential carbon-dioxide sorption was observed on a cadmium based mixed-linker metal-organic framework (MOF){[Cd(abdc)(azpy)](DMA)}n [where 4,4´-azopyridine = azpy and 2-amino-1,4-benzenedicarboxylic acid = H2abdc]. {[Cd(abdc)(azpy)](DMA)}n features an interpenetrated 3D networked structure consist of pendant Lewis basic −NH2 groups directed towards the pores. PLATON analysis shows that the solvent accessible void space of the MOF is ca. 26.6%. At 298 K, the desolvated MOF showed an uptake of carbon-dioxide of 8.33 wt% or 42.42 cc/g at 1 bar pressure which, upon cooling to 273 K, is increased to about 12.17 wt% or 62 cc/g at 1 bar pressure. In contrast, methane uptake capacities of the desolavated MOF were 0.127 wt% or 1.79 cm3/g and 1.34 wt% or 18.74 cm3/g at the adsorbate pressure of 1 bar at 298 K and 273 K, respectively. On the otherhand, hydrogen uptake capacity of the desolavated MOF reached to 0.31 wt% or 34.87 cm3/g at the adsorbate pressure of 1 bar at 77 K. Selectivity of carbon-dioxide with respect to methane at 273 K is calculated to be 5.4. The heat of adsorption for carbon-dioxide is calculated to be 38 kJmol− 1.
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Debnath, R., Ghosh, P. & Koner, S. Preferential CO2 adsorption over cadmium-based Porous Metal-organic Framework. J Porous Mater 30, 1163–1170 (2023). https://doi.org/10.1007/s10934-022-01409-9
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DOI: https://doi.org/10.1007/s10934-022-01409-9