Self-assembled nanoflower-mediated interfacial polymerization through tunable intra- and inter-layer channels to boost total heat exchange performance

Abstract

Total heat exchange membranes (THEMs) are vital for minimizing energy consumption and enhancing indoor air quality in energy recovery ventilation (ERV) systems. Manipulating the surface morphology of polyamide (PA) membranes via nanofiller-mediated interfacial polymerization is key to advancing total heat recovery performance. This study presented the fabrication of PA thin-film nanocomposite (TFN) membranes by integrating self-assembled poly(amic acid-imide) nanoflowers (P(AA-I)-NFs) with intertwined nanosheets into the organic phase. This facile approach effectively eliminated nonselective interphase voids and defects, owing to the superior polymer affinity of the organic nanoflowers. The finely tuned intra- and inter-layer channels within P(AA-I)-NFs significantly impacted monomer mass transfer, facilitated the shuttle effect, expanded the interfacial polymerization zone, and led to the formation of a rougher, thicker PA layer with enhanced surface area. The optimized P(AA-I)-NFs/PA TFN membranes exhibited outstanding performance, including CO₂ permeability of 0.51 GPU, water vapor permeability of 656.59 GPU, and an enthalpy exchange efficiency of 71.47 %, surpassing the trade-off limitations typically observed in commercial and other advanced THEMs. These findings underscored the potential of P(AA-I)-NFs-mediated TFN membranes as highly competitive candidates for next-generation ERV systems.