Adsorption performance of the functional COFs for removal of bisphenol A: Molecular dynamic simulations

Abstract

The inherent structural features of the covalent organic frameworks (COFs) play a crucial role in determining their adsorption performances for bisphenol A (BPA). The computational methods were advantageous in unraveling intrinsic molecular properties about their performances. Herein, some COFs with different functional groups (–COOH, –NH2, –NO2 and –CF3) were designed to demonstrate the efficacy of the functional COFs for adsorbed BPA in gas phase and aqueous solution. The density functional theory (DFT) and Grand Canonical Monte Carlo (GCMC) methods were used to analyze the interaction energy between COFs and BPA, structure properties, and adsorption performances etc.. The results indicated that the addition of strong electronegative functional groups in COFs increased these COFs’ isosteric heat of adsorption (Qst) (TpBD-(COOH)2 > TpBD-(CF3)2 > TpBD-(NH2)2 > TpBD-(NO2)2 > TpBD) for gas phase BPA, but their introduction also reduced the pore size of COFs (TpBD > TpBD-(COOH)2 > TpBD-(NH2)2 > TpBD-(CF3)2 > TpBD-(NO2)2). However, these functional COFs demonstrated the stronger the adsorption capacity for gas phase BPA (At 298 K and 1 bar, the BPA uptake of TpBD-(COOH)2, TpBD-(NH2)2, TpBD, TpBD-(NO2)2 and TpBD-(CF3)2 was 242.52, 232.43, 219.31, 206.64 and 197.73 mg/g, respectively.). The amount of BPA adsorbed by functional COFs was the result of the synergistic effect of the electronegativity of functional groups and the pore size. Molecular dynamic (MD) simulation performed the same phenomenon for BPA in aqueous solution. In addition, the higher temperature will decrease the adsorption amount of BPA by COF, but increase its desorption ability.