Levels of naturally occurring radioisotopes in local and imported bottled drinking water available in Québec City, Canada.

Consumption of local and imported bottled water in Canada has greatly increased during the past three decades. While the presence of natural radioactivity is often overlooked when dealing with the water quality of these bottled products, it could contribute substantially to the uptake of radionuclides especially when sourced from regions with higher radioactivity levels compared to where it is consumed. In this study, the activity of several naturally occurring radionuclides (i.e., 210Po, 226,228Ra, 230,232Th, 234,235,238U) were measured in bottled water available in Québec, Canada after sample pretreatment and analysis by either radiometric or mass spectrometry approaches. 230,232Th and 228Ra concentrations were below minimum detectable activity levels in all samples tested. Analytical results for 234U, 235U, 238U, and 226Ra showed concentrations that ranged from 0.38 to 115 mBq/L, (2.2-313) x 10-2 mBq/L, 0.48-58.4 mBq/L, and 1.1-550 mBq/L, respectively. 210Po was detected in only 5 samples and its activity ranged from 2 to 26 mBq/L. To determine variability in activity within brands, the same brands of bottled water were purchased during two consecutive years and analyzed. The possible radiological impact of the consumption of these types of water was assessed based on different drinking habit scenarios. Some of the imported water brands showed higher activity concentrations than local sources or tap water, suggesting that individuals drinking predominantly imported bottled water would receive a higher radiation dose than those who drink mainly local water.

A rapid sequential chromatographic separation of U- and Th-decay series radionuclides in water samples.

A new sequential protocol for the separation and preconcentration of U, Th, Ra, Po and Pb for the same sample aliquot has been designed. The optimized stacking of chromatographic resins [TRU, Sr and a new hybrid Ra resin (composed of Analig Ra-01 and cation exchange AG50Wx8)] enables a rapid loading of the sample (less than 75 min for 300 mL of samples) while ensuring a high retention of the analytes of interest. The use of a hybrid Ra resin allows the complete and selective extraction of Ra on a solid support, a feature lacking in other sequential separation procedures. A loading medium composed of 1 M HNO3 and chloride ions (as NH4Cl) was found suitable for the retention of all analytes of interest onto the stacked chromatographic resins. The proposed elution conditions facilitate the complete segregation of individual elements in 5 distinctive fractions, reducing the risk of spectral and non-spectral interferences. This feature enables the proper quantification of the radioisotopes either by ICP-MS or alpha spectrometry below national and international regulatory guidelines. The mean chemical recoveries for the separation are 93, 98, 105, 88, and 98% for U, Th, Ra, Po and Pb, respectively. Reproducible yields were obtained independently of the water type tested, demonstrating the versatility and the robustness of the proposed methodology.