4.7 Article

Evolutional solid phase and solid-liquid interface uranium immobilization mechanisms by nanoscale zero-valent iron and enhanced uranium stability control strategy

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 453, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.139924

Keywords

Nanoscale zero-valent iron; Uranium stability; Uranium wastewater; Continuous flow stirred tank reactor; Eh control strategy

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Uranium is a carbon dioxide free nuclear energy, but uranium-contained wastewater has negative health effects on humans. Nanoscale zero-valent iron (nZVI) has the ability to separate uranium from wastewater with high efficiency. The study investigates the transformation mechanisms of nZVI and its effect on uranium binding. The findings can help improve the remediation of uranium-contained wastewater using nZVI technology.
Uranium is a carbon dioxide free nuclear energy, and uranium-contained wastewater poses serious chronic health effects toward human. Nanoscale zero-valent iron (nZVI) separates uranium from wastewater with ul-trafast kinetic, high capacity and selectivity. However, the dynamic interfacial uranium binding mechanisms and its stability, controlled by the phase transformation of nZVI, is important but poorly understood. After 120 h reaction, the fresh nZVI was oxidized and transformed to ferrihydrite and then lepidocrocite and hematite. Analysis for the structures and valence states of U, Fe species indicated that the dominate U(VI) uptake mech-anism changed from Fe0 induced reduction to adsorption as nZVI transformed to iron (oxyhydr)oxides. Density functional theory calculation revealed that uranyl formed corner-sharing configurations on the surface of iron nanoparticles, and some uranium ions prefer to incorporate into the structure of lepidocrocite than hematite during the crystallization processes of ferrihydrite. Meanwhile, 100 -10000 mu g/L uranyl ions were quickly captured, the residual uranium could be maintained at-9.31 mu g/L and the content of uranium in reacted iron nanoparticles reached-24.16 wt%. Interestingly, the oxidization reduction potential (Eh) was a potential parameter to control uranium immobilization in the CSTR system, and the Eh control strategy could be used to increase the fraction of U(IV)/U(V), sparingly soluble and highly stable, higher than 90 %. The findings augment our understanding of U-nZVI reactions and guide nZVI technology to remedy real uranium-contained wastewater.

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