| Literature DB >> 28219248 |
Zhongtang Wang1, Jian Zheng1, Youyi Ni1,2, Wu Men1, Keiko Tagami1, Shigeo Uchida1.
Abstract
Plutonium is extensively studied in radioecology (e.g., soil to plant transfer and radiological assessment) and geochemistry (e.g., sediment dating). Here, we reported a new chemical separation method for rapid determination of Pu in soil and sediment samples, based on the following investigations: extraction behaviors of interfering elements (IEs, for inductively coupled plasma mass spectrometry (ICPMS) measurement) on TEVA resin; decontamination of U using TEVA, UTEVA, and DGA resins; and the impact of coprecipitation on Pu determination. The developed method consists of four steps: HNO3 leaching for Pu release; CaF2/LaF3 coprecipitation for the removal of major metals and U; the proposed TEVA + UTEVA + DGA procedure for the removal of U, Pb, Bi, Tl, Hg, Hf, Pt, and Dy; and ICPMS measurement. The accuracy of this method in determining 239+240Pu activity and 240Pu/239Pu and 241Pu/239Pu isotopic ratios was validated by analyzing five standard reference materials (soil, fresh water sediment, and ocean sediment). This method is characterized by its stable and high Pu recovery (90-97% for soil; 92-98% for sediment) and high decontamination factor of U (1.6 × 107), which is the highest reported for soil and sediment samples. In addition, the short analytical time of 12 h and the method detection limits, which are the lowest yet reported in literature, of 0.56 μBq g-1 (0.24 fg g-1) for 239Pu, 1.2 μBq g-1 (0.14 fg g-1) for 240Pu, and 0.34 mBq g-1 (0.09 fg g-1) for 241Pu (calculated on the basis of a 1 g soil sample) allow the rapid determination of ultratrace level Pu in soil and sediment samples.Entities:
Year: 2017 PMID: 28219248 DOI: 10.1021/acs.analchem.6b04975
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986