TY - JOUR
T1 - Scalable regeneration of damaged polyamide membranes via self-assembled biomass coatings for sustainable water treatment
AU - Hao, Wen
AU - Wang, Huan
AU - Hui, Haiqing
AU - Li, Jing
AU - Ma, Hongpeng
AU - Lee, Jaewoo
AU - Zhang, Qiuyu
AU - Tian, Miao
N1 - Publisher Copyright:
© 2026 Elsevier B.V.
PY - 2026/8
Y1 - 2026/8
N2 - Thin-film composite polyamide (TFC-PA) membranes are widely used in water purification, yet oxidative and operational damage often drive premature disposal and replacement. This study presents a scalable two-step aqueous regeneration strategy that reconstructs damaged PA surfaces using a redox-triggered, lysozyme-derived biomass interlayer (BDI) followed by polyethyleneimine (PEI) functionalization. The BDI forms a cohesive proteinaceous priming nanofilm that restores surface continuity and provides multivalent anchoring sites for PEI, yielding an amine-rich, charge-governed interface. Applied to damaged nanofiltration membranes, the regenerated membranes achieve high Li+/Mg2+ selectivity (S Li/Mg = 128.1) with Mg2+ rejection exceeding 99.5% while maintaining practical water transport. The strategy is further extended to end-of-life reverse osmosis (RO) elements, where regeneration recovers desalination performance with a water permeance of 3.5 ± 0.5 L m−2 h−1 bar−1 and NaCl/MgCl2 rejections of 92.8 ± 0.1% and 96.8 ± 0.5%, respectively, demonstrating competitive performance relative to a commercial NF benchmark. Long-term filtration in complex waters confirms enhanced fouling/scaling tolerance and regeneration-enabled recoverability after oxidative challenge via surface reconstruction. An element-level cost assessment estimates a chemical cost of $12.87 per 8-inch module, highlighting the potential for low-cost membrane reuse and reduced lifecycle impacts for sustainable water treatment.
AB - Thin-film composite polyamide (TFC-PA) membranes are widely used in water purification, yet oxidative and operational damage often drive premature disposal and replacement. This study presents a scalable two-step aqueous regeneration strategy that reconstructs damaged PA surfaces using a redox-triggered, lysozyme-derived biomass interlayer (BDI) followed by polyethyleneimine (PEI) functionalization. The BDI forms a cohesive proteinaceous priming nanofilm that restores surface continuity and provides multivalent anchoring sites for PEI, yielding an amine-rich, charge-governed interface. Applied to damaged nanofiltration membranes, the regenerated membranes achieve high Li+/Mg2+ selectivity (S Li/Mg = 128.1) with Mg2+ rejection exceeding 99.5% while maintaining practical water transport. The strategy is further extended to end-of-life reverse osmosis (RO) elements, where regeneration recovers desalination performance with a water permeance of 3.5 ± 0.5 L m−2 h−1 bar−1 and NaCl/MgCl2 rejections of 92.8 ± 0.1% and 96.8 ± 0.5%, respectively, demonstrating competitive performance relative to a commercial NF benchmark. Long-term filtration in complex waters confirms enhanced fouling/scaling tolerance and regeneration-enabled recoverability after oxidative challenge via surface reconstruction. An element-level cost assessment estimates a chemical cost of $12.87 per 8-inch module, highlighting the potential for low-cost membrane reuse and reduced lifecycle impacts for sustainable water treatment.
KW - Biomass-derived interlayer
KW - Membrane regeneration
KW - Polyamide membrane
KW - Polyethyleneimine grafting
KW - Sustainable water treatment
UR - https://www.scopus.com/pages/publications/105041194595
U2 - 10.1016/j.memsci.2026.125747
DO - 10.1016/j.memsci.2026.125747
M3 - 文章
AN - SCOPUS:105041194595
SN - 0376-7388
VL - 756
JO - Journal of Membrane Science
JF - Journal of Membrane Science
M1 - 125747
ER -