Demonstrates enhanced uranium extraction capacity from seawater using copper-modified fibers, suggesting a cost-effective solution.
Polymer fibers are leading adsorbents for large-scale uranium extraction from seawater, yet their performance is hindered by microbial adhesion and an “emergent phenomenon” in which excessive ligand induces hydrogen-bond-driven microphase aggregation of polymer chains, limiting ligand accessibility. Herein, we develop a trace nanometal-driven surface microstructure engineering strategy to address these challenges. As a proof of concept, trace Cu/Cu x O nanoparticles are incorporated into PAO-grafted polyethylene fibers (CuPAO@PE) through in situ coordination during radiation-induced graft polymerization. Incorporation of only 0.2 wt % Cu/Cu x O nanoparticles effectively modulates polymer aggregation, creating abundant mesopores (∼5.2 nm). Consequently, CuPAO@PE exhibits a 9-fold increase in uranyl ion diffusion depth and a 23.8% enhancement in adsorption capacity, achieving 819.6 mg g –1 in single uranium solution compared with copper-free fibers (PAO@PE). The optimized microstructure, coupled with the antibacterial activity of Cu/Cu x O, enables CuPAO@PE to maintain robust antibiofouling performance and achieve 5.1 mg g –1 uranium uptake after six months in natural seawater. These improvements in adsorption and antibiofouling performance are achieved with only a 0.4% increase in material cost relative to PAO@PE. This work provides a cost-effective, scalable solution to simultaneously enhance adsorption performance, offering broader design insights for the development of efficient adsorbents for challenging marine environments.
No takes yet. Share an insight, caveat, or question.
Liu et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: