Thin film composite polyamide (TFC)
nanofiltration (NF)
membranes
represent extensive applications at the water-energy-environment nexus,
which motivates unremitting efforts to explore membranes with higher
performance. Intrusion of polyamide into substrate pores greatly restricts
the overall membrane permeance because of the excessive hydraulic
resistance, while the effective inhibition of intrusion remains technically
challenging. Herein, we propose a synergetic regulation strategy of
pore size and surface chemical composition of the substrate to optimize
selective layer structure, achieving the inhibition of polyamide intrusion
effective for the membrane separation performance enhancement. Although
reducing the pore size of the substrate prevented polyamide intrusion
at the intrapore, the membrane permeance was adversely affected due
to the exacerbated “funnel effect”. Optimizing the polyamide
structure via surface chemical modification of the substrate, where
reactive amino sites were in situ introduced by the ammonolysis of
polyethersulfone substrate, allowed for maximum membrane permeance
without reducing the substrate pore size. The optimal membrane exhibited
excellent water permeance, ion selectivity, and emerging contaminants
removal capability. The accurate optimization of selective layer is
anticipated to provide a new avenue for the state-of-the-art membrane
fabrication, which opens opportunities for promoting more efficient
membrane-based water treatment applications.