Economic Monitoring of Uranium in Drinking and Mineral Water

Analytical instrumentation

Economic Monitoring of Uranium in Drinking and Mineral Water

13 Nov, 2008

Published over 17 years ago. See the latest and most current information on Analytical instrumentation.

Determining trace levels of uranium in drinking and mineral water by inductively coupled plasma mass spectroscopy (ICP-MS) requires
expensive analytical instrumentation. In contrast, adsorptive cathodic stripping voltammetry (AdCSV) using Metrohm`s 797 VA Computrace is a straightforward, much less expensive alternative allowing measurements with superior sensitivity.
Uranium is radioactive, toxic and a suspected teratogen. While different national health authorities prescribe limits in drinking water ranging from 0 up to 10 ìg/L, the World Health Organization (WHO) recommends a concentration limit of 15 ìg/L.
The AdCSV method for the voltammetric determination of the uranium content is based on complexing U(VI) with chloranilic acid (CAA)
at a pH between 1.8 and 2.5. After preconcentration of the uranium-chloranilic acid complex at the working electrode, the uranium content
can be determined down to the ng/L range by using the differential pulse measuring technique (DP). The determination of uranium(VI) is
specific and selective, as the positive deposition potential means that other metal-CAA complexes or organic matrix components of natural
waters are either not adsorbed on the working electrode or hardly adsorbed at all. The German standard DIN 38406-17 is currently being
drawn up based on this AdCSV method. This means that in future the voltammetric determination of uranium can be used as a generally
recognised method for monitoring drinking and mineral water in daily practice.

PIN 27.2 Apr/May 2026

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