Skip to main content
Log in

Determination of thorium and uranium in activated concrete by inductively coupled plasma mass spectrometry after anion-exchange separation

  • Original Paper
  • Published:
Fresenius' Journal of Analytical Chemistry Aims and scope Submit manuscript

Abstract

A sensitive analytical method was established for the determination of Th and U in activated concrete samples. The method combines an anion-exchange separation step with an ICP-MS determination technique. In the ICP-MS measurement, a few μg mL–1 of Al and Ca, a few ng mL–1 of Mn, La, Ce, Nd and Pb and pg mL–1 amounts of Li, Zr, Nb and Ba coexisting in the anion-exchange fraction of Th and U did not interfere. No adverse interference effects were observed in real sample analyses. The obtained detection limits (3σ, n = 10) of Th and U were 2.3 and 1.8 pg mL–1, respectively. The analytical precisions for ca. 5 μg g–1 Th and ca. 1 μg g–1 U in real activated concrete samples were equally less than 7% RSD. The accuracies obtained by the analysis of GSJ rock standard samples were –18.1 to 0.4% for the Th determination and –14.0 to –5.7% for the U determination. The method uses the conventional absolute calibration curve. The internal standard calibration is unnecessary.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: 14 March 1999 / Revised: 13 July 1999 / Accepted: 15 July 1999

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kato, K., Ito, M. & Watanabe, K. Determination of thorium and uranium in activated concrete by inductively coupled plasma mass spectrometry after anion-exchange separation. Fresenius J Anal Chem 366, 54–58 (2000). https://doi.org/10.1007/s002160050011

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s002160050011

Keywords

Navigation