Aluminum-based metal-organic frameworks for adsorptive removal of anti-cancer (methotrexate) drug from aqueous solutions

A series of metal-organic frameworks (MOFs) based on aluminum-benzene dicarboxylates (MIL-53, NH2-MIL-53, and NH2-MIL-101) at different ratios have been synthesized, and their adsorption performances for methotrexate (MTX), an anti-cancer drug, have been investigated in terms of adsorption kinetics, isotherms, solution pH, thermodynamics, mechanism, and recyclability. Maximum adsorption values of 374.97, 387.82, and 457.69 mg/ g were observed for MIL-53, NH2-MIL-53, and NH2-MIL-101 , respectively. Our study shows that adsorption capacity of MTX depends not only on surface area and pore volume but also on the zeta potential and the presence of suitable functional groups. Higher adsorption of NH2-MIL-101 observed for MTX than the other synthesized MOFs may be attributed to its large surface area, large total pore volume, high positive zeta potential, and polar amino functional groups located on its surface, which are responsible for its increased interactions with MTX molecules. Adsorption isotherms and kinetics of MTX onto NH2-MIL-101 followed the Langmuir and pseudo-second-order kinetic equations. Thermodynamic data suggest that adsorption of MTX onto NH2-MIL-101 is spontaneous and exothermic, while the adsorption mechanism is governed by electrostatic interactions, pi-pi stacking interactions, and H-bonding. Regeneration and recyclability of NH2-MIL-101 were also investigated by washing with ethanol to observe its decreased adsorption performance towards MTX. It was slightly decreased after seven adsorption-desorption cycles, indicating excellent regeneration and good structural stability under the chosen experimental conditions.

Automated summary

The study found that NH2-MIL-101 has a higher adsorption capacity for MTX compared to other synthesized MOFs due to its large surface area, total pore volume, positive zeta potential, and polar amino functional groups. Adsorption of MTX onto NH2-MIL-101 follows Langmuir isotherms and pseudo-second-order kinetic equations. Thermodynamic data suggest that adsorption onto NH2-MIL-101 is spontaneous and exothermic, with electrostatic interactions, pi-pi stacking, and H-bonding playing a role in the adsorption mechanism.