This study employs molecular dynamics simulations to investigate the influence of functionalized UiO-66 materials (with -H, -NH2, -NO2, and -(OH)2 groups) on the adsorption and diffusion behaviors of ethanol and waste oil before transesterification reactions. A multi-scale modeling approach, including a three-layer interfacial model, surface adsorption, and intra-framework adsorption, was utilized to systematically evaluate the effects of functionalization on structural properties, molecular diffusion, adsorption performance, and interfacial interactions. The simulation results reveal that functionalization enhances the intrinsic diffusivity of the metal–organic framework but generally suppresses the diffusion of ethanol and waste oil. The -(OH)2 group exhibits the most significant diffusion hindrance due to steric effects and strong hydrogen bonding. Adsorption of waste oil is dominated by coordination and hydrophobic interactions, while ethanol adsorption relies on hydrogen bonding. Within the framework, functionalization does not improve ethanol adsorption capacity; instead, pristine UiO-66 shows the highest uptake due to its optimal pore size. Adsorption energy calculations on the (002) surface indicate that the -NO2 group exhibits the strongest affinity for oleic acid, owing to its strong electronegativity and synergistic effects with metal sites. For polyunsaturated fatty acids, adsorption performance depends critically on the compatibility between the hydrophobic pore environment and molecular conformation. Ethanol adsorption is governed primarily by hydrogen bonding and metal coordination. This study provides molecular-level insights into the structure–function relationships governing pre-reaction adsorption and mass transport mechanisms of functionalized UiO-66 in transesterification reactions, providing a theoretical foundation for the rational design of efficient pre-reaction microenvironments in biodiesel catalysts.
Wen et al. (2026) studied this question.