Abstract

The increasing amounts of emerging contaminants (ECs) in aquatic ecosystems are becoming one of the serious environmental issues. Therefore, the efficient removal of ECs is of urgent importance. Herein, a computational technique of molecular dynamics (MD) and the density functional theory (DFT) were employed to assess the adsorption affinity of three regenerable covalent organic frameworks (COFs), namely, DAAQ-TFP, COF-78, and COF-OEt, for the removal of six different ECs from the different pharmaceutical groups, including atenolol, carbamazepine, ciprofloxacin, diclofenac, ibuprofen, and gemfibrozil. Detailed analyses showed that DAAQ-TFP and COF-78 were more efficient in removing atenolol (100%) and carbamazepine (100%) with Gibbs free energy values of −24.48 and −21.15 kJ/mol, respectively. COF-OEt possessed the highest absolute value of the Gibbs free energy, interaction energy, and adsorption affinity in removing ciprofloxacin (88%), diclofenac (63%), ibuprofen (100%), and gemfibrozil (100%). The hydrogen bond formation and van der Waals forces were introduced as the primary adsorption mechanisms. In addition, it was shown that COFs with a pore-based structure have lower capability for the removal of pollutants. The primary aim of this research work is to introduce efficient and regenerable COFs as a promising adsorbent for the removal of pharmaceutical pollutants.

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