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The sustainable development of nuclear energy requires a secure long-term uranium supply. Seawater uranium extraction offers a nearly inexhaustible resource; however, its commercialization is limited due to high costs. To improve economic viability, this study proposes a synergistic strategy for simultaneously recovering uranium and vanadium using amidoxime-based adsorbents, with vanadium as a valuable co-product. Herein, a porous silica-supported poly(amidoxime) adsorbent was synthesized and characterized. The material possesses a well-developed porous structure with a specific surface area of 49.8 m2 g−1. Spectroscopic analyses confirmed the successful grafting of amidoxime groups onto the silica framework, whereas X-ray photoelectron spectroscopy revealed that uranium adsorption occurs via coordination with nitrogen and oxygen donor atoms. Batch experiments demonstrated rapid adsorption equilibrium within 2 h and a maximum Langmuir uranium capacity of 48.5 mg g−1 at 45 °C. The adsorbent exhibited high selectivity toward uranium over vanadium and competing ions at near-neutral pH. Dynamic column experiments demonstrated efficient stepwise separation using 0.1 mol L−1 HNO3 for uranium and a Na2CO3–H2O2 system for vanadium, even in simulated seawater containing high concentrations of competing ions. Under the controlled model conditions employed, this study demonstrates a promising adsorbent and a feasible co-recovery strategy that may contribute to enhancing the economic feasibility of seawater uranium extraction, warranting further validation in natural seawater.
Jiao et al. (Thu,) studied this question.