Abstract
Heavy metal contamination of drinking water remains a persistent global challenge, exacerbated by salinity, industrial discharge, and the limitations of existing membrane technologies that are constrained by permeability-selectivity trade-offs. In this study, we develop a hybrid thin film nanocomposite (TFN) forward osmosis (FO) membrane by incorporating a zirconium-based metal-organic framework (UiO-66) and its conductive polymer-functionalized analogue (PANI@UiO-66) into the polyamide active layer via interfacial polymerization. The incorporation of UiO-66 enhances water transport through the introduction of hydrophilic microporous domains, while the polyaniline coating modulates nanoscale transport pathways and interfacial interactions. Systematic variation in filler type and loading reveals distinct functional roles of the two fillers. Membranes incorporating bare UiO-66 exhibit increased water flux, attributed to facilitated transport through MOF-derived nanochannels, but show a moderate increase in reverse solute flux. In contrast, PANI@UiO-66 incorporation results in reduced water flux but significantly suppresses reverse solute flux and enhances chromium rejection, indicating improved control over selective transport. At an optimal loading of 0.15 wt% (TFN-PU3), the membrane demonstrates an improved balance between water permeability and solute selectivity compared to the pristine thin film composite (TFC) membrane under FO conditions. The observed performance is attributed to the combined effects of modified transport pathways and interfacial interactions introduced by the hybrid filler system. The results highlight the potential of conductive polymer-MOF hybridization as a strategy for tuning membrane performance. This work provides a practical framework for designing TFN membranes for selective heavy-metal removal in saline and complex water environments.