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Updated: Jan 20, 2026

Separation of Uranium and Thorium for 230Th-U Dating of Submarine Hydrothermal Sulfides
Published on: May 20, 2019
Determination of Femtogram-Level Plutonium Isotopes in Environmental and Forensic Samples with High-Level Uranium
Xiaolin Hou1,2,3,4, Weichao Zhang1,5, Yanyun Wang1,5
1State Key Laboratory of Loess and Quaternary Geology, Shaanxi Key Laboratory of Accelerator Mass Spectrometry Technology and Application, Xi'an AMS Center , Institute of Earth Environment, Chinese Academy of Sciences , Xi'an 710061 , China.
Abstract:
ICP-MS is becoming a competitive technique for measurement of plutonium isotopes. Besides the abundance sensitivity (tailing of 238U to m/z = 239 and 240), isobaric and polyatomic ions interferences (e.g., 238U1H+) are the most critical challenges for determination of low-level plutonium in high uranium samples. This work presents a new method to solve this problem using ICP-MS with two tandem quadrupole separators and a dynamic collision/reaction cell combined with chemical separation. The interference of uranium hydrides (238U1H+ and 238U1H2+) was effectively eliminated using CO2 as reaction gas by converting hydrides to oxides of uranium ions (UO+/UO2+) but still keeping the intensity of the Pu+ signal. The tailing interference of 238U+ (abundance sensitivity) was intensively eliminated by significantly suppressing the 238U+ signal using CO2 as reaction gas and using two tandem quadrupole mass separators in the ICP-MS/MS. With these approaches the overall interference of uranium was reduced to <1 × 10-8, which is 3 orders of magnitude better than the conventional ICP-MS. Combined with chemical separation with a decontamination factor of 105 for uranium, an overall factor of 1012 for elimination of uranium interference was achieved. The developed method was demonstrated to enable accurate determination of <10-15 g/g level plutonium isotopes in environmental samples even in a uranium debris sample with a U/Pu atomic ratio of up to 1012. The developed method was validated by analysis of a spiked solution and certified reference materials of soil.
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