Methods determined the decontamination factor of uranium and the recovery of rare earth elements, indicating their effectiveness.
Rare earth elements (REEs) have significant application value in the quality control of nuclear materials and in traceability research in nuclear forensics. Methods were developed for the determination of REEs in uranium-bearing nuclear materials. The digestion parameters for uranium oxides and uranium ores, such as the digestion acid, digestion temperature, and digestion time, were optimized and reported. The optimized digestion parameters for uranium oxides were 2 mL HNO3 at 160 °C for 3 h, and those for uranium ores were 7 mL mixed acid (HNO3–HClO4–HF = 5:5:3) at 180 °C for 36 h. Two digestion methods were demonstrated to be effective for the quantitative recovery of REEs. The suitable system and specifications for different resin columns were investigated to achieve a high decontamination factor of U (105) by UTEVA resin. The corresponding loading system was 10 mL 4 M HNO3, and the elution system was 6 mL 4 M HNO3. Additionally, the analysis of ultra-trace REEs in high-uranium matrices was accomplished using two UTEVA resins. The developed methods were subjected to the Cochran test and the Grubbs test, and the relative standard deviation (RSD) for all REEs was below 6%. In uranium oxide samples with different spiked amounts, the recovery of REEs exceeded 80% in all cases, and the RSDs were all less than 10%. The method’s detection limits were below 10 ppt for all REEs (except for Ce), ensuring the accurate measurement of REEs in uranium-bearing nuclear materials.
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Li et al. (2025) studied this question.
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