Issue 6, 1992

Determination of traces of neptunium-237 in enriched uranium solutions using inductively coupled plasma mass spectrometry

Abstract

A procedure using inductively coupled plasma mass spectrometry (ICP-MS) has been developed for determining traces of 237Np in isotopically enriched solutions of U. The chemical treatment of the samples consists of: extracting 237Np in a 1 mol dm–3 solutions of nitric acid using 0.5 mol dm–3 thenoyltrifluoroacetone in xylene, leaving 99% of the U matrix in the aqueous phase; re-extracting 237Np in 10 mol dm–3 nitric acid; heating the extracted solution to white fumes in order to remove the excess of acid; and diluting the resulting solution with 2% HNO3. Optimization of the analytical parameters involved suppressing the spectral overlap between 237Np and 238U. By applying an additive continuous tension to the quadrupole on m/z 237 only, the interfering part of the 238U peak is eliminated and good resolution can be achieved between m/z 237 and 238, if the concentration of U is less than 100 mg dm–3. The operating conditions adopted result from a compromise between resolution and sensitivity. The suppression of the analyte signal, arising from U at a high concentration, is corrected for by adding an internal standard to the calibration and measuring solutions. The detection limit is about 0.005 µg of Np per gram of U, for an initial sample of 1 g of U and an additive continuous tension of 7.5 V. The analytical performance of ICP-MS is compared with that of α-spectrometry. The radiochemical determination of 237Np involves a tedious pre-treatment and measurement procedure. In contrast, ICP-MS appears to be a good alternative to α-spectrometry (for the determination of long-lived radionuclides) because of its simplicity, accuracy, excellent detection limits and rapidity of analysis.

Article information

Article type
Paper

J. Anal. At. Spectrom., 1992,7, 923-927

Determination of traces of neptunium-237 in enriched uranium solutions using inductively coupled plasma mass spectrometry

C. Riglet, O. Provitina, J. Dautheribes and D. Revy, J. Anal. At. Spectrom., 1992, 7, 923 DOI: 10.1039/JA9920700923

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements