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A method to determine the absolute activity of 137Cs in irradiated nuclear fuel is presented. Using a well-known point-like calibration source in combination with measurements of the gamma-ray intensity from the nuclear fuel and Monte Carlo calculations based on the nominal measurement geometry, the activity content can be determined without prior knowledge of the intrinsic detection efficiency of the gamma-ray detector. The presented method is tested using measurements of the 137Cs intensity from spent nuclear fuel of the pressurized water type at the central interim storage in Sweden. Using an assumption of homogeneous distribution of 137Cs throughout the fuel, we demonstrate a linear relationship between measured activity and the activity calculated by a state-of-the-art simulation code. For future studies, we suggest some factors that potentially can decrease the uncertainty in the correlation between measured and calculated activity.

The reliable detection of neutrons in a harsh gamma-ray environment is an important aspect of establishing non-destructive methods for the characterization of spent nuclear fuel. In this study, we present results from extended in-situ monitoring of detector systems consisting of commercially available components: EJ-426, a 6Li-enriched solid-state scintillator material sensitive to thermal neutrons, and two different types of Hamamatsu photomultiplier tubes (PMT). Over the period of eight months, these detectors were operated in close vicinity to spent nuclear fuel stored at the interim storage facility CLAB, Oskarshamn, Sweden. At the measurement position the detectors were continuously exposed to an estimated (moderated) neutron flux of approx. 280 n/s cm 2 and a gamma-ray dose rate of approximately 6 Sv/h. Using offline software algorithms, neutron pulses were identified and characterized in the data. Over the entire investigated dose range of up to 35 kGy, the detector systems were functioning and were delivering detectable neutron signals. Their performance as measured by the number of identified neutrons degrades down to about 30% of the initial value. Investigations of the irradiated components suggest that this degradation is a result of reduced optical transparency of the involved materials as well as a reduction of PMT gain due to the continuous high currents. Increasing the gain of the PMT through step-ups of the applied high voltage allowed to partially compensate for this loss in detection sensitivity even when the detectors were highly irradiated. The integrated neutron fluence during the measurement was experimentally verified to be in the order of 5 × 10 9 n cm −2 . The results were interpreted with the help of MCNP6.2 simulations of the setup and the neutron flux.

Raw data from calorimetric measurements of five nuclear fuel assemblies of the PWR 17 × 17 type are provided. Measurements of the temperature both inside a calorimeter, in which the fuel assembly was placed, as well as outside, were performed as a function of time while water circulating inside the calorimeter heats up from radiation emitted in the radioactive decay of material in the fuel assembly. The data contain also measurements of dose rate in the water outside the calorimeter. Data from 38 measurements using an electrically heated model of a fuel assembly are also provided to be used for, e.g., calibration. The data can be used for validation of computer codes for modelling of nuclear systems, e.g. nuclear reactors, storage and transport of nuclear fuel or systems for geological disposal.

Spent nuclear fuel comprises a wide range of irradiated isotopic material compositions, and characterization through nondestructive measurements is beneficial in verifying declared parameters before the fuel is placed in storage, final disposal, and/or reprocessed. This paper discusses results from three nondestructive assay instruments, including passive gamma, passive neutron, and active neutron methods, that measured fifty spent fuel assemblies at the Clab interim storage facility in Sweden. Integrated analysis of the measurements from the three different instruments allowed parametric assessments of cooling time, burnup, neutron multiplication, fissile mass, initial enrichment, and decay heat of each individual fuel assembly. Passive gamma measurements were found to be the most beneficial in predicting cooling time, passive neutron for determining burnup, active neutron in estimating initial enrichment, and both passive and total neutron for multiplication correlations. Fissile mass was best estimated using any combination of any two of the instruments such that corrections for isotopic changes in the fuel could be accounted for with the first set of measurements and multiplication of the assembly in the second. In conclusion, the nondestructive assay technologies demonstrated through this effort enhance the characterization of spent nuclear fuel assemblies.

Using a high-purity Germanium gamma-ray energy spectroscopic detector system, time-stamped list-mode data sets were acquired during axial scanning of 19 boiling water reactor (BWR) and 28 pressurized water reactor (PWR) type of nuclear fuel assemblies. The data sets were collected during two measurements campaigns in September 2016 and March 2019 at the Central Interim Storage Facility for Spent Nuclear (Clab) in Sweden. A certified calibration source of 137Cs was positioned along the central line of sight between the measured fuel assembly and the detector. Data sets from measurements with only the calibration source and other background sources, i.e. without a nuclear fuel assembly present, are also included. The list-mode structure of the measured data allows for an axially-resolved as well as energy-spectral resolved intensity of nuclide-specific gamma lines emitted from the spent nuclear fuel. Data presented here can be used e.g. for validation of gamma-ray transport simulation tools or for development of methods to estimate parameters of the spent nuclear fuel based on data from gamma-ray spectroscopy.

Differential Die-Away Self-Interrogation (DDSI) is a method by which the characteristic die-away of neutrons from spontaneous and induced fissions is used to characterize a spent nuclear fuel assembly. A nondestructive assay (NDA) instrument was built at Los Alamos National Laboratory to implement and test the DDSI method. The DDSI instrument contains 3He detectors which measure thermal neutrons, and the time and location of detection of each neutron is recorded via list-mode data acquisition. The instrument was sent to the Clab interim storage facility in Sweden for measurement and characterization of 50 spent pressurized water reactor (PWR) and boiling water reactor (BWR) fuel assemblies. The result was over 40 h of neutron list-mode data from a wide variety of fuel assemblies with high enough efficiency to perform neutron coincidence counting, i.e. detection of time-correlated neutrons from fission. Analysis algorithms for characterization of the fuel assemblies were tested on the Swedish spent fuel dataset. Using the measured data, multiplication, fissile mass, initial enrichment, burnup, and total plutonium mass were determined in the 50 assemblies with root mean square errors ranging from 1.5% for PWR multiplication to 11.4% for BWR fissile mass. The results in this work demonstrate that the DDSI concept is capable of characterizing spent power reactor fuel with levels of accuracy that are compatible with the requirements and objectives of various applications such as safeguards verification or facility material control and accounting.

A project to research the application of non-destructive assay (NDA) techniques for spent fuel assemblies is underway at the Central Interim Storage Facility for Spent Nuclear Fuel (for which the S ...