Nitrogen-containing
compounds (NCCs) such as indole (IND) and quinolone
(QUI) in a model fuel were adsorbed over pristine and variously functionalized
metal–organic frameworks (MOFs) (here, UiO-66 and −NH2, −NH3
+, −COOH, −COONa,
−OH, −SO3H functionalized UiO-66s) to quantitatively
understand the interactions between the adsorbates (IND and QUI) and
UiO-66s. The adsorbed quantity of IND and QUI increased linearly with
increasing number of H-acceptors and H-donors (for H-bond), respectively,
on UiO-66s (excluding one MOF for each adsorption), confirming the
importance of H-bonding in the adsorption. UiO-66-NH3
+ and UiO-66-NH2 showed a deviated trend in the
IND and QUI adsorption, respectively; this might be explained by cation−π
interactions and base–base repulsion, respectively. Moreover,
the QUI adsorption increased linearly with increasing number of acidic
sites on the MOFs (excluding basic ones), also suggesting the importance
of acid–base interactions. Finally, UiO-66-NH3
+ showed the highest adsorption for both IND and QUI among
the studied MOFs, suggesting that introducing an ammonium group on
MOFs can be one way to develop a competitive adsorbent for the adsorptive
denitrogenation of fuels.