A Microporous Zn(bdc)(ted) 0.5 with Super High Ethane Uptake for Efficient Selective Adsorption and Separation of Light Hydrocarbons.

Separating light hydrocarbons (C2 H6 , C3 H8 , and C4 H10 ) from CH4 is challenging but important for natural gas upgrading. A microporous metal-organic framework, Zn(bdc)(ted)0.5 , based on terephthalic acid (bdc) and 1,4-diazabicyclo[2.2.2]octane (ted) ligands, is synthesized and characterized through various techniques, including powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and porosity analysis. The adsorption isotherms of light hydrocarbons on the material are measured and the isosteric adsorption heats of CH4 , C2 H6 , C3 H8 , and C4 H10 are calculated. The prediction of C2-4/C1 adsorption selectivities is accomplished using ideal adsorbed solution theory (IAST). The results indicate that the material exhibits exceptional characteristics, including a Brunauer-Emmett-Teller (BET) surface area of 1904 m2 /g and a pore volume of 0.73 cm3 /g. Notably, the material demonstrates remarkable C2 H6 adsorption capacities (4.9 mmol/g), while CH4 uptake remains minimal at 0.4 mmol/g at 298 K and 100 kPa. These findings surpass those of most reported MOFs, highlighting the material's outstanding performance. The isosteric adsorption heats of C2 H6 , C3 H8 , and C4 H10 on the Zn(bdc)(ted)0.5 are higher than CH4 , suggesting a stronger interaction between C2 H6 , C3 H8 , and C4 H10 molecules and Zn(bdc)(ted)0.5 . The molecular simulation reveals that Zn(bdc)(ted)0.5 prefers to adsorb hydrocarbon molecules with richer C-H bonds and larger polarizability, which results in a stronger dispersion force generated by an adsorbent-adsorbate induced polarization effect. Therefore, the selectivity of C4 H10 /CH4 is up to 180 at 100 kPa, C3 H8 /CH4 selectivity is 67, and the selectivity of C2 H6 /CH4 is 13, showing a great potential for separating C2-4 over methane.