Lori A. Metz
Pacific Northwest National Laboratory
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Publication
Featured researches published by Lori A. Metz.
Journal of Radioanalytical and Nuclear Chemistry | 2015
Shannon M. Morley; Brienne N. Seiner; Erin C. Finn; Lawrence R. Greenwood; Steven C. Smith; Stephanie J. Gregory; Morgan M. Haney; Dawn D. Lucas; Leah M. Arrigo; Tere A. Beacham; Kevin J. Swearingen; Judah I. Friese; Matthew Douglas; Lori A. Metz
Mixed fission and activation materials resulting from various nuclear processes and events contain a wide range of isotopes for analysis spanning almost the entire periodic table. This work describes the production of a complex synthetic sample containing fission products, activation products, and irradiated soil, and determines the percent chemical recovery of select isotopes through the integrated chemical separation scheme. Based on the results of this experiment, a complex synthetic sample can be prepared with low atom/fission ratios and isotopes of interest accurately and precisely measured following an integrated chemical separation method.
Journal of Astm International | 2012
Lawrence R. Greenwood; Richard S. Wittman; Bruce D. Pierson; Lori A. Metz; Rosara F. Payne; Erin C. Finn; Judah I. Friese
A boron carbide capsule has been designed and used for spectral-tailoring experiments at the TRIGA reactor at Washington State University. Irradiations were conducted in pulsed mode and in continuous operation for up to 4 h. A cadmium cover was used to reduce thermal heating. The neutron spectrum calculated with the Monte Carlo N-particle transport code was found to be in good agreement with reactor dosimetry measurements using the STAY’SL computer code. The neutron spectrum resembles that of a fast reactor. The design of a capsule using boron carbide fully enriched in 10B shows that it is possible to produce a neutron spectrum similar to that of 235U fission.
Journal of Environmental Radioactivity | 2014
Ted W. Bowyer; Paul W. Eslinger; Ian M. Cameron; Judah I. Friese; James C. Hayes; Lori A. Metz; Harry S. Miley
The monitoring of the radioactive xenon isotopes (131m)Xe, (133)Xe, (133m)Xe, and (135)Xe is important for the detection of nuclear explosions. While backgrounds of the xenon isotopes are short-lived, they are constantly replenished from activities dominated by the fission-based production of (99)Mo used for medical procedures. At present, one of the most critical locations on earth for the monitoring of nuclear explosions is the Korean peninsula where the Democratic Peoples Republic of Korea (DPRK) has announced that it conducted three nuclear tests between 2006 and 2013. This paper explores the backgrounds that would be caused by the medium to large scale production of (99)Mo in the region of the Korean peninsula.
Archive | 2011
Erin C. Finn; Lori A. Metz; Rosara F. Payne; Judah I. Friese; Lawrence R. Greenwood; Jeremy D. Kephart; Bruce D. Pierson; Tere A. Ellis
A unique set of fission product gamma spectra was collected at short times (4 minutes to 1 week) on various fissionable materials. Gamma spectra were collected from the neutron-induced fission of uranium, neptunium, and plutonium isotopes at thermal, epithermal, fission spectrum, and 14-MeV neutron energies. This report describes the experimental methods used to produce and collect the gamma data, defines the experimental parameters for each method, and demonstrates the consistency of the measurements.
Separation Science and Technology | 2011
Lori A. Metz; Rosara F. Payne; Mark D. Engelmann
Low-level analysis of radioiodine performed by TIMS requires an initial chemical separation from interfering higher electron-affinity halogens. Experiments using 125I and 36Cl tracers have shown that iodide can be selectively oxidized and purged from solution while the chloride remains in the solution. A systematic investigation of the experimental factors that affect the oxidation and transfer of iodine along with the separation of iodide from chloride has been completed. Experimental design was used to determine the optimum experimental conditions by obtaining a better understanding of factor affects and interactions. Factors such as gas purge rate, experiment run time, and oxidant concentration were simultaneously studied in a central composite design of experiments and response surfaces were generated from results. Optimizing experimental factors resulted in improved iodide oxidation and transfer efficiencies, halogen separation, and shorter analysis times.
Journal of Radioanalytical and Nuclear Chemistry | 2017
Samuel S. Morrison; Sue B. Clark; Tere A. Eggemeyer; Erin C. Finn; Corey C. Hines; Mathew D. King; Lori A. Metz; Shannon M. Morley; Mathew S. Snow; Donald E. Wall; Brienne N. Seiner
This work describes a radiochemical separation procedure for the determination of gold (Au), platinum (Pt), tantalum (Ta), and tungsten (W) activation in the presence of fission products. Chemical separations result in a reduction in the minimum detectable activity by a factor of 287, 207, 141, and 471 for 182Ta, 187W, 197Pt, and 198Au respectively, with greater than 90% recovery for all elements. These results represent the highest recoveries and lowest minimum detectable activities for 182Ta, 187W, 197Pt, and 198Au from mixed fission-activation product samples to date, enabling considerable refinement in the measurement uncertainties for neutron fluences in highly complex sample matrices.Graphical Abstract
Journal of Radioanalytical and Nuclear Chemistry | 2016
Brienne N. Seiner; Andy R. King; Erin C. Finn; Lawrence R. Greenwood; Lori A. Metz; Judah I. Friese; Olivia Marsden; Ashley V. Davies; Philip Scivier
The fission products from HEU formed under a fast-pooled neutron spectrum generated using a boron carbide shield were analyzed at Pacific Northwest National Laboratory and the Atomic Weapons Establishment. The results from each laboratory using chemical separation, high-purity germanium gamma spectroscopy and/or Compton suppression gamma spectroscopy are compared with the potential benefits and limitations of the different gamma spectroscopy methods discussed.
Journal of Radioanalytical and Nuclear Chemistry | 2013
Lori A. Metz; Judah I. Friese; Erin C. Finn; Lawrence R. Greenwood; Rosara F. Kephart; Corey C. Hines; Matthew D. King; Kelley Henry; Donald E. Wall
Journal of Radioanalytical and Nuclear Chemistry | 2009
Lori A. Metz; Rosara F. Payne; Judah I. Friese; Lawrence R. Greenwood; Jeremy D. Kephart; Bruce D. Pierson
Journal of Radioanalytical and Nuclear Chemistry | 2014
Brienne N. Seiner; Shannon M. Morley; Tere A. Beacham; Morgan M. Haney; Stephanie J. Gregory; Lori A. Metz