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Research Article | Open Access

Dual-active-site PDA@PW12 microspheres for high-efficiency uranium extraction via synergistic complexation and reduction

Yu LiuLimin ZhangDonghui CuiXue YangXiao LiangKeyu ChenFengyan Li ( )
Key Laboratory of Polyoxometalate and Reticular Material Chemistry of Ministry of Education, College of Chemistry, Northeast Normal University, Changchun 130024, China
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Abstract

In this study, polydopamine@phosphotungstic acid composite microspheres for efficient uranium adsorption were successfully prepared through the in situ copolymerization of dopamine and phosphotungstic acid. Characterization results showed that the incorporation of phosphotungstic acid inhibited the agglomeration of polydopamine and increased the specific surface area to 48.07 m2/g while simultaneously generating W5+ active species through electron transfer. The prepared material achieved a maximum uranium adsorption capacity of 720.1 mg/g at pH = 5 and 318 K, with the adsorption following the pseudo-second-order kinetic model and Langmuir isotherm model, indicating spontaneous monolayer chemisorption. Mechanistic investigations confirmed that uranium adsorption occurred through the synergistic effect of surface complexation with functional groups (–OH/–NH2) and the reduction of U(VI) to U(IV) by W5+ species. The composite maintained 93.3% desorption efficiency after five adsorption–desorption cycles and exhibited excellent selectivity toward U(VI). Thus, this work provides a promising strategy for the development of high-performance uranium adsorbents.

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Polyoxometalates
Article number: 9140119

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Cite this article:
Liu Y, Zhang L, Cui D, et al. Dual-active-site PDA@PW12 microspheres for high-efficiency uranium extraction via synergistic complexation and reduction. Polyoxometalates, 2026, 5(2): 9140119. https://doi.org/10.26599/POM.2026.9140119

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Received: 08 December 2025
Revised: 30 December 2025
Accepted: 18 January 2026
Published: 27 February 2026
© The Author(s) 2026. Published by Tsinghua University Press.

Open Access This article is licensed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, sharing, distribution and reproduction in any medium, provided the original work is properly cited.