Abstract

This article describes a novel and simple method to measure ultra-trace 226Ra in river water samples at fg L−1 (mBq L−1) levels as a means for surveying 226Ra in an unintended contamination in river water. To simplify the procedure, a single column was used for separation and purification; 10 mL of AG 50W-X8 resin was packed into a 10 mL Eppendorf pipette tip, which was used as a separation column. A 500 mL sample solution was loaded, and interfering elements were removed with 80 mL 4 M HCl in 20% ethanol. Subsequently, Ra together with Ba was eluted by 20 mL 5 M HNO3 prior to SF-ICP-MS analysis; this allows the naturally existing Ba in water samples to be employed as a yield tracer for 226Ra analysis. Using the medium mode of SF-ICP-MS, the instrumental detection limit of 380 fg L−1 (10 mBq L−1) was obtained. An extremely low method detection limit of 0.46 fg L−1 (0.02 mBq L−1) was achieved with 500-fold pre-concentration. Finally, the developed technique was applied to analyze natural water samples collected from Japanese rivers, in which the 226Ra concentrations varied in the range of 0.7–49.6 fg L−1 (0.03–1.82 mBq L−1).

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.