Abstract
A Ti-incorporated metal organic framework structure, MIL-125, and its amine-functionalized form, NH2-MIL-125, were synthesized via a solvothermal route aided by microwave heating. The samples were characterized by XRD, SEM, TGA, EA, UV–vis spectroscopy, and N2 adsorption–desorption measurements. MIL-125 was unstable in aqueous solution, but NH2-MIL-125 was stable both in water and in heptane; its hydrophilic property was further confirmed by water vapor adsorption. NH2-MIL-125 showed moderate CO2 adsorption capacity (136mgg−1) but excellent selectivity over N2 (>27:1) at 298K with a low heat of adsorption surpassing the performance of MIL-125. Four consecutive CO2 adsorption–desorption cycles over NH2-MIL-125 showed completely reversible adsorbent regeneration at 298K under a helium flow for a total duration of 550min. Catalytic properties of the materials were evaluated by cycloaddition of epichlorohydrin and oxidative desulfurization of dibenzothiophene. Finally, batch mode liquid-phase competitive separation of isoprene from 2-methyl butane was conducted, revealing high selectivity of isoprene against 2-methyl butane (ca. 7.8 and 9.7) over MIL-125 and NH2-MIL-125, respectively.
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