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Trace Elemental Analysis of Bulk Thorium Using an Automated Separation–Inductively Coupled Plasma Optical Emission Spectroscopy Methodology
Author(s) -
Benjamin T. Manard,
Shalina C. Metzger,
Sarah K. Wysor,
Veronica C. Bradley,
Benjamin D. Roach,
N. Alex Zirakparvar,
Kayron T. Rogers,
Debra A. Bostick,
Brian W. Ticknor,
Cole R. Hexel
Publication year - 2020
Publication title -
applied spectroscopy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.415
H-Index - 110
eISSN - 1943-3530
pISSN - 0003-7028
DOI - 10.1177/0003702820961390
Subject(s) - inductively coupled plasma atomic emission spectroscopy , thorium , elemental analysis , inductively coupled plasma , analytical chemistry (journal) , chemistry , spectroscopy , matrix (chemical analysis) , trace element , inductively coupled plasma mass spectrometry , actinide , impurity , materials science , mass spectrometry , plasma , uranium , chromatography , nuclear chemistry , metallurgy , physics , inorganic chemistry , nuclear physics , organic chemistry , quantum mechanics
Presented here is a novel automated method for determining the trace element composition of bulk thorium by inductively coupled plasma-optical emission spectroscopy (ICP-OES). ICP-OES is a universal approach for measuring the trace elemental impurities present in actinide-rich materials; however, due to the emission rich spectrum of the actinide, a separation from the trace elements is warranted for spectrochemical analysis. Here, AG MP-1 ion exchange resin was utilized for retention of the Th matrix, while allowing the trace element impurities to be separated prior to subsequent analysis using ICP-OES. After demonstrating the separation on traditional gravity-driven columns, the methodology was transitioned to an automated platform for comparison. This automated platform utilizes syringe-driven sample and solvent flow and can collect the trace element and thorium fractions in separate locations. While reducing the sample size (500 µL, 1.5 mg of Th), maintaining the overall separation efficiency (recoveries >95%), and illustrating the sample throughput ability (n = 10+), this automated methodology could be readily adopted to nuclear facilities in which the determination of trace elemental impurities in Th samples is warranted.

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