Enhanced mechanism of calcium towards uranium incorporation and stability in magnetite during electromineralization.

J Hazard Mater

School of Resource & Environment and Safety Engineering, University of South China, Hengyang 421001, China; State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620, China. Electronic address: hy

Published: September 2023


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Doping uranium into a room-temperature stable FeO lattice structure effectively reduces its migration. However, the synergistic or competitive effects of coexisting ions in an aqueous solution directly affect the uranium mineralization efficiency and the structural stability of uranium-bearing FeO. The effects of calcium, carbonate, and phosphate on uranium electromineralization were investigated via batch experiments and theoretical calculations. Calcium incorporated into the FeO lattice increased the level and stability of doped uranium in FeO. Uranium and calcium occupied the octahedral and tetrahedral sites of FeO, respectively; the formation energy was only -10.23 eV due to strong hybridization effects between Fe1s, U4f, O2p, and Ca3d orbitals. Compared to the uranium-doped FeO, uranium leaching ratios decreased by 19.2 % and 48.9 % under strongly acidic and alkaline conditions after 120 days. However, high concentrations of phosphate inhibited FeO crystallization. These results should provide new avenues for the development of multi-metal co-doping technologies and mineralization optimization to treat uranium-containing complex wastewater.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jhazmat.2023.131641DOI Listing

Publication Analysis

Top Keywords

feo lattice
8
feo uranium
8
uranium
7
feo
7
enhanced mechanism
4
calcium
4
mechanism calcium
4
calcium uranium
4
uranium incorporation
4
incorporation stability
4

Similar Publications

Regulating Bimetallic Asymmetry of Mn-O-Fe Domain in Layered Double Hydroxides for Lattice Oxygen Activation toward Enhanced Photocatalytic Toluene Oxidation.

Inorg Chem

September 2025

State Key Laboratory of Water Pollution Control and Green Resource Recycling, School of Environment, Key Laboratory of Mesoscopic Chemistry of MOE, Institute of Theoretical and Computational Chemistry, School of Chemistry and Chemical Engineering, Jiangsu Key Laboratory of Vehicle Emissions Control,

In photocatalytic toluene oxidation, traditional semiconductor catalysts still face the problem of insufficient generation of reactive oxygen species (ROS). Herein, we first regulate the bimetallic asymmetry in layered double hydroxide (LDH) photocatalysts via different metal electronegativities to activate lattice oxygen for ROS generation. The MnFe-LDH, MnAl-LDH, and ZnFe-LDH photocatalysts with various electronegativities (Mn: 1.

View Article and Find Full Text PDF

Controlling the non-stoichiometry is an effective way to tune physicochemical properties of functional oxides and explore novel physical phenomena in complex oxides. Therefore, quantitative control of oxygen non-stoichiometry in perovskite oxides plays an important role in understanding the mechanism of topotactic phase transition and improving the applicability of electrochemical devices. Here, an electrochemical titration cell is fabricated to control the oxygen non-stoichiometry of a BiCaFeO thin film grown on yttria-stabilized zirconia substrate.

View Article and Find Full Text PDF

Room-temperature FeSi-doped CuSe thermoelectric films with enhanced figure of merit.

Sci Rep

July 2025

Data-Driven Inorganic Materials Group, Center for Basic Research on Materials, National Institute for Materials Science (NIMS), 1-2-1 Sengen, Tsukuba, Ibaraki, 305-0047, Japan.

Thermoelectric (TE) materials offer a promising pathway toward achieving carbon neutrality by converting waste heat into electricity. The enhancement of their figure-of-merit (zT) depends on optimizing the composition of materials and nanostructures, reducing the thermal conductivity, and increasing the power factor. CuSe, a superionic material, achieves a zT of 0.

View Article and Find Full Text PDF

Influence of biomass ashes on the structural evolution and oxygen-donating capacity of red mud during chemical looping gasification.

Waste Manag

August 2025

Key Laboratory of Coal Processing, Efficient and Clean Utilization, Ministry of Education, School of Chemical Engineering and Technology, China University of Mining and Technology, Xuzhou 221116, China. Electronic address:

To efficiently convert the biomass wastes, chemical looping gasification has been proposed as a highly effective method to produce hydrogen-rich syngas. The lattice oxygens in oxygen carriers can supplant molecular oxygens, thereby improving syngas quality. However, the complex interactions between oxygen carrier and biomass ash are inevitable, obviously affecting reactivity of oxygen carrier.

View Article and Find Full Text PDF

In-Situ Atomic-Scale Revelation of Amorphous Metallic Iron Formation during Hydrogen-Driven Reduction of Iron Oxides.

ACS Appl Mater Interfaces

July 2025

Department of Mechanical Engineering & Materials Science and Engineering Program, Binghamton University, State University of New York, Binghamton, New York 13902, United States.

The transition to hydrogen as a green reductant in metal production is critical for decarbonizing the metallurgical industry, yet atomic-scale mechanisms governing reduction pathways and phase evolution remain unresolved. Using in situ environmental transmission electron microscopy, we identify a hidden pathway that reveals dynamic formation of amorphous metallic iron (Fe) during the hydrogen-driven reduction of ferrous oxides of FeO and FeO. Real-time imaging uncovers three coexisting transformation routes: (i) FeO → FeO, (ii) FeO → amorphous Fe, and (iii) FeO → amorphous Fe.

View Article and Find Full Text PDF