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For the past 10 y Health Canada has operated a Fixed Point Surveillance Network of NaI(Tl) detectors across Canada. Deployed for both emergency response and daily monitoring of airborne radiation in the environment, a spectral stripping method allowed measurement of certain isotopes well below the ambient dose rate. These include 133Xe, 135Xe and 41Ar, typical of emissions from operating nuclear reactors. In an effort to increase the number of isotopes measured at these low levels a new technique of spectral fitting using spectral templates is being implemented. However, this requires very accurate spectral templates that can be difficult or impossible to obtain empirically for environmental measurements of airborne radio-isotopes. Therefore, a method of efficiently using Monte Carlo techniques to create these templates was developed. [ABSTRACT FROM AUTHOR]

A global monitoring system for atmospheric xenon radioactivity is being established as part of the International Monitoring System that will verify compliance with the Comprehensive Nuclear-Test-Ban Treaty (CTBT) once the treaty has entered into force. This paper studies isotopic activity ratios to support the interpretation of observed atmospheric concentrations of 135Xe, 133mXe, 133Xe and 131mXe. The goal is to distinguish nuclear explosion sources from civilian releases. Simulations of nuclear explosions and reactors, empirical data for both test and reactor releases as well as observations by measurement stations of the International Noble Gas Experiment (INGE) are used to provide a proof of concept for the isotopic ratio based method for source discrimination. [ABSTRACT FROM AUTHOR]

Strontium isotopes, (89)Sr and (90)Sr, and (226)Ra being radiotoxic when ingested, are routinely monitored in milk and drinking water samples collected from different regions in Canada. In order to monitor environmental levels of activity, a novel semi-automated sensitive method has been developed at the Radiation Protection Bureau of Health Canada (Ottawa, Canada). This method allows the separation and quantification of both (89)Sr and (90)Sr and has also been adapted to quantify (226)Ra during the same sample preparation procedure. The method uses a 2-stage purification process during which matrix constituents, such as magnesium and calcium that are rich in milk, are removed as well as the main beta-interferences (e.g., (40)K, (87)Rb, (134)Cs, (137)Cs, and (140)Ba). The first purification step uses strong cation exchange (SCX) chromatography with commercially available resins. In a second step, fractions containing the radiostrontium analytes are further purified using high-performance ion chromatography (HPIC). While (89)Sr is quantified by Cerenkov counting immediately after the second purification stage, the same vial is counted again after a latent period of 10-14 days to quantify the (90)Sr activity based on (90)Y ingrowth. Similarly, the activity of (226)Ra, which is separated by SCX only, is determined via the emanation of (222)Rn in a 2-phase aqueous/cocktail system using liquid scintillation counting. The minimum detectable concentration (MDC) for (89)Sr and (90)Sr for a 200 min count time at 95% confidence interval is 0.03 and 0.02 Bq/L, respectively. The MDC for (226)Ra for a 100 min count time is 0.002 Bq/L. Semi-annual intercomparison samples from the USA Department of Energy Mixed Analyte Performance Evaluation Program (MAPEP) were used to validate the method for (89)Sr and (90)Sr. Spiked water samples prepared in-house and from International Atomic Energy Agency (IAEA) were used to validate the (226)Ra assay., (Crown Copyright © 2010. Published by Elsevier Ltd. All rights reserved.)

Over 300 daily environmental radioxenon samples were analyzed using French developed SPALAX for automatic sample preparation including high-resolution gamma-spectrometry. The 133Xe sensitivity was significantly better than 1 mBq/m3 (specified criterion for Comprehensive Nuclear-Test-Ban Treaty verification). Radioxenon analysis was extended to include the X-ray region by improved detector window, sample cell design, efficiency calibration, line shape fitting and background analysis. The resulting analysis offers a 4-16 fold improvement in sensitivity for 133mXe and 131mXe, respectively.