Journal
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY
Volume 28, Issue 8, Pages 1283-1287Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3ja50121c
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Funding
- Ministry of Education, Culture, Sports, Science and Technology, Japan
- Grants-in-Aid for Scientific Research [25800301] Funding Source: KAKEN
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A method was developed for the determination of I-129 in soil samples using a Triple Quadrupole ICP-MS, with the objective of investigating radioiodine released by the Fukushima Daiichi Nuclear Power Plant (FDNPP) accident. The determination of I-129 by ICP-MS is capable of providing a high sample throughput compared to other methods. Nonetheless, the high background caused by Xe-129 impurities in argon plasma gas and polyatomic ions such as (IH2+)-I-127 and (ID+)-I-127 has made it difficult to carry out determinations of this isotope by conventional ICP-MS instruments. In this study, oxygen was used as a reaction gas for reducing the background intensity of m/z 129, principally by Xe-129. The contribution of polyatomic ions such as (IH2+)-I-127 and (ID+)-I-127 could be effectively corrected for by assuming a production ratio of 5 x 10(-9). The detection limit for I-129 in solution was successfully improved. The measured I-129/I-127 ratios in NIST SRM 3231 Level II standard solution are consistent with the certified value of 0.981 x 10(-8) within the analytical error, suggesting the reliability of the method to the measurement of I-129/I-127. In order to confirm the applicability of this method to the measurement of I-129/I-127 ratios of Fukushima soils, samples were collected for analysis from 5-60 km away from the FDNPP. Prior to the ICP-MS measurement iodine fractions were separated from soil by pyrohydrolysis and were purified by solvent extraction. The I-129/I-127 ratios in the samples are consistent with values determined by accelerator mass spectrometry (AMS) within the analytical error. This method provides a powerful tool for the investigation of radioiodine contamination in Fukushima and elsewhere.
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