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Droessler, Janelle E.

Publications and source records attributed to Droessler, Janelle E..

Separation of rare earth element radioisotopes by reverse-phase high-speed counter-current chromatography

Analytical scale purification of rare earth element (REE) radioisotopes is typically accomplished using cation-exchange resins (e.g. AG 50W-X8) and high-performance liquid chromatography (HPLC). Despite the variety of improvements made since the development of this separation process in the 1950s, nearest neighbor separations remain a challenge, as does the issue of irreversible sample adsorption. Herein, we report a study that evaluates the potential of high-speed counter-current chromatography (HSCCC) as an alternative method for purifying REE elements, with specific reference to separations of fission product REE of interest to nuclear forensics. Complementary HSCCC REE separation experiments, one spiked with radiotracer and REE fission product activity, allowed for in depth analysis of resulting fractions from both an elemental (inductively coupled plasma atomic emission spectroscopy, ICP-AES) and radiological (gamma-ray spectrometry, beta counting) purity perspective. The highly reproducible nature of separation profiles generated from HSCCC instruments was leveraged to simplify work-up of samples containing radioisotopes. Subsequent radioanalytical evaluation revealed minimal carryover of Eu into neighboring Sm and Tb fractions (as indicated by presence of 150Eu), and trace contamination of the Tb fraction with Y (as indicated by presence of 91Y). Subtle differences in stationary phase retention across the two columns were reflected in significant variations in decontamination factors of duplicate parallel separations. Furthermore, these differences paired with obtained distribution of radioisotopes provided valuable insights into future improvements. Collectively, this study represents a significant step forward in development of HSCCC technology for task specific REE radioisotope purification.

07 ISOTOPE AND RADIATION SOURCES↗

Cs[Tf 2 N]: a second polymorph with a layered structure

The structural determination of the ionic liquid, caesium bis[(trifluoromethyl)sulfonyl]imide or poly[[μ 4 -bis[(trifluoromethyl)sulfonyl]imido]caesium(I)], Cs[N(SO 2 CF 3 ) 2 ] or Cs[Tf 2 N], reveals a second polymorph that also crystallizes in a layer structure possessing monoclinic P 2 1 / c symmetry at 120 K instead of C 2/ c for the known polymorph [Xue et al. (2002). Solid State Sci. 4 , 1535–1545]. The caesium ions in the cationic layers are coordinated by the sulfonyl groups of the bistriflimide molecules from anion layers while the trifluoromethyl groups are oriented in the opposite direction, forming a non-polar surface separating the layers. The layer direction is (100).

36 MATERIALS SCIENCE↗