Search

The emanation of radionuclides has been highlighted as a known source of uncertainty in the estimation of radionuclide source signatures from underground nuclear tests and other nuclear activities, particularly in the case of activation products. A system was developed at Pacific Northwest National Laboratory to quantify the emanation of argon from two powders and five rock types ranging in particle size from powder to small rocks. Samples were neutron irradiated and the percent emanation of 37Ar was measured to range between 0.3 and 25%. Measurements were also made of the 39Ar emanation for four of these materials and was found to be consistently lower than that of 37Ar.

An algorithm was developed to improve the quantification of metastable isotopes in the presence of 133Xe. Radioxenon emissions are commonly used to monitor for nuclear explosions. When 133Xe is present in these samples it causes interference in the activity calculation of the metastable isotopes. The alternative analysis method analyzes the anticoincidence spectrum of the plastic detector to decrease interference from 133Xe. Simulation results show that the anticoincidence analysis accurately quantifies the activity of 131mXe. For the data analyzed here, the anticoincidence method identifies 83% more samples above the minimum detectable activity than the traditional method.

In order to make predictions of the potential 37Ar signal from an underground nuclear explosion, a value for the 37Ar emanation fraction is needed. A system was developed to quantify the emanation fraction from samples ranging in size from powder to small rocks. Assorted rock samples were irradiated with Watt fission spectrum neutrons to produce radioactive argon gas via activation of calcium. The argon produced was extracted on a custom apparatus and cryogenically trapped. The extracted gas was then processed to separate the argon and load it into a proportional counter for counting. The emanation fraction of argon gas from the rock samples was then calculated by comparing the measured and predicted activities.

The aim of this paper is to compare radioxenon beta–gamma analysis algorithms using simulated spectra with experimentally measured background, where the ground truth of the signal is known. We believe that this is among the largest efforts to date in terms of the number of synthetic spectra generated and number of algorithms compared using identical spectra. We generate an estimate for the minimum detectable counts for each isotope using each algorithm. The paper also points out a conceptual model to put the various algorithms into a continuum. Our results show that existing algorithms can be improved and some newer algorithms can be better than the ones currently used.

Beta–gamma coincidence radioxenon detectors must be calibrated for each of the four-radioxenon isotopes (135Xe, 133Xe, 133mXe, and 131mXe). Without a proper calibration, there is potential for the misidentification of the amount of each isotope detected. It is important to accurately determine the amount of each radioxenon isotope, as the ratios can be used to distinguish between an anthropogenic source and a nuclear explosion. We have developed a xenon calibration system (XeCalS) that produces calibration spikes of known activity and pressure for field calibration of detectors. We will present results from the development of XeCalS and a portable spike implementation system.

A Noble Gas Migration Experiment injected 127Xe, 37Ar, and sulfur hexafluoride into a former underground nuclear explosion shot cavity. These tracer gases were allowed to migrate from the cavity to near-surface and surface sampling locations and were detected in soil gas samples collected using various on-site inspection sampling approaches. Based on this experiment we came to the following conclusions: (1) SF6 was enriched in all of the samples relative to both 37Ar and 127Xe. (2) There were no significant differences in the 127Xe to 37Ar ratio in the samples relative to the ratio injected into the cavity. (3) The migratory behavior of the chemical and radiotracers did not fit typical diffusion modeling scenarios.

PNNL developed a beta–gamma simulator (BGSim) that incorporated GEANT-modeled data sets from radioxenon decay chains, as well as functionality to use nuclear detector-acquired data sets to create new beta–gamma spectra with varying amounts of background, 133Xe, 131mXe, 133mXe, 135Xe, and 222Rn and its decay products. After BGSim was developed, additional uses began to be identified for the program output: training sets of two-dimensional spectra for data analysts at the IDC and other NDC, and spectra for exercises such as the Integrated Field Exercise 2014 held in Jordan at the Dead Sea.

Fission product yields are critical data for a variety of nuclear science and engineering applications; however, independent yields have not been extensively measured to date. We have previously documented a methodology to measure the cumulative and independent fission product yields using gamma spectrometry and nuclide buildup and decay modeling, and numerical optimization. We have produced fission products by bombarding 235U with 14.1 MeV neutrons and made measurements of fission product yields. In this paper, we summarize our approach, describe initial experiments, and present preliminary results where we have determined nine fission product yields for long-lived nuclides.

As part of the verification component of the Comprehensive Nuclear-Test-Ban Treaty (CTBT), environmental gas samples originating from nuclear fission are analyzed for the presence of 131mXe, 133mXe, 133Xe, and 135Xe. In this work, the non-traditional radioxenon isotope 125Xe was investigated. The isotope was produced as an isotopically pure sample via neutron activation of 124Xe at the University of Texas at Austin Nuclear Engineering Teaching Lab’s TRIGA MARK II Reactor. The sample was then measured using a HPGe detector as well as an ARSA-style β–γ coincidence detector. Potential sources and sensitivities for production of 125Xe are also considered for relevance to the CTBT verification mission.

Uncertainties associated with short lived (half-lives less than 1 day) fission product yields listed in databases such as the National Nuclear Data Center’s ENDF/B-VII are large enough for certain isotopes to provide an opportunity for new precision measurements to offer significant uncertainty reductions. A series of experiments has begun where small samples of 235U are irradiated with a pulsed, fission neutron spectrum at the Nevada National Security Site and placed between two broad-energy germanium detectors. The amount of various isotopes present immediately following the irradiation can be determined given the total counts and the calibrated properties of the detector system. The uncertainty on the fission yields for multiple isotopes has been reduced by nearly an order of magnitude.

Radioxenon emissions from fission-based radiopharmaceutical production are a major source of background concentrations affecting the radioxenon detection systems of the international monitoring system (IMS). Collection of real-time emissions data from production facilities makes it possible to screen out some medical isotope signatures from the IMS radioxenon data sets. This paper describes an effort to obtain and analyze real-time stack emissions data with the design, construction and installation of a small stack monitoring system developed by a joint CTBTO-IDC, BATAN, and Pacific Northwest National Laboratory team at the BaTek medical isotope production facility near Jakarta, Indonesia.

For ensuring compliance with a Comprehensive Nuclear-Test-Ban Treaty, it is essential to have advanced monitoring technologies for the detection of nuclear testing and to ensure that detected signals are well understood. Traditionally, 131m Xe, 133m/g Xe, and 135Xe originating from fission are analyzed to determine their possible origin. This work explores the non-traditional isotope 127Xe (T 1/2 = 36.346(3) d) as it can occur as emission from research reactors, is used in medical procedures, and tracer experiments. It is a good candidate for quality assurance and control and inter-laboratory comparisons. 127Xe was produced via neutron activation and measured with a high purity germanium detector as well as a β–γ-coincidence detector system.