Passive Neutron Albedo Reactivity (PNAR) is one of fourteen techniques that has been researched and evaluated to form part of a comprehensive and integrated detection system for the non-destructive assay (NDA) of spent nuclear fuel. PNAR implemented with 3He tubes for neutron detection (PNAR-3He) is the measurement of time correlated neutrons from a spent fuel assembly with and without a Cadmium (Cd) layer surrounding the assembly. PNAR utilizes the self-interrogation of the fuel via reflection of neutrons born in the fuel assembly back in to the fuel assembly. The neutrons originate primarily from spontaneous fission events within the fuel itself (Curium-244) but are amplified by multiplication. The presence and removal of the Cd provides two measurement conditions with different neutron energy spectra and therefore different interrogating neutron characteristics. Cd has a high cross-section of absorption for slow neutrons and therefore greatly reduces the low energy (thermal) neutron fluence rate returning. The ratios of the Singles, Doubles and Triples count rates obtained in each case are known as the Cd ratios, which are related to fissile content. A potential safeguards application for which PNAR-3He is particularly suited is 'fingerprinting'. Fingerprinting could function as an alternative to plutonium (Pu) mass determination; providing confidence that material was not diverted during transport between sites. PNAR-3He has six primary NDA signatures: Singles, Doubles and Triples count rates measured with two energy spectra at both shipping and receiving sites. This is to uniquely identify the fuel assembly, and confirm no changes have taken place during transport. Changes may indicate all attempt to divert material for example. Here, the physics of the PNAR-3He concept will be explained, alongside a discussion on the development of a prototypical PNAR-3He instrument using simulation. The capabilities and performance of the conceptual instrument will be summarized, in the context of (a) quantifying Pu mass in spent fuel assemblies and (b) detecting pin diversion (through a discrepancy between declared and measured properties of the fuel assembly) when the instrument is deployed. These quantitative capabilities are complementary to the 'fingerprinting' capability which is part of ensuring continuity of knowledge and custody of spent nuclear fuel.

An integrated nondestructive assay instrument, which combined the Passive Neutron Albedo Reactivity (PNAR) and the Self-Interrogation Neutron Resonance Densitometry (SINRD) techniques, is the research focus for a collaborative effort between Los Alamos National Laboratory (LANL) and the Japanese Atomic Energy Agency as part of the Next Generation Safeguard Initiative. We will quantify the anticipated performance of this experimental system in two physical environments: (1) At LANL we will measure fresh Low Enriched Uranium (LEU) assemblies for which the average enrichment can be varied from 0.2% to 3.2% and for which Gd laced rods will be included. (2) At Fugen we will measure spent Mixed Oxide (MOX-B) and LEU spent fuel assemblies from the heavy water moderated Fugen reactor. The MOX-B assemblies will vary in burnup from ≈3 GWd/tHM to ≈20 GWd/tHM while the LEU assemblies (≈1.9% initial enrichment) will vary from ≈2 GWd/tHM to ≈7 GWd/tHM. The estimated count rates will be calculated using MCNPX. These preliminary results will help the finalization of the hardware design and also serve a guide for the experiment. The hardware of the detector is expected to be fabricated in 2012 with measurements expected to take place in 2012 and 2013. This work is supported by the Next Generation Safeguards Initiative, Office of Nuclear Safeguards and Security, National Nuclear Security Administration.

The DDA instrument for nuclear safeguards is a fast, non-destructive assay, active neutron interrogation technique using an external 14 MeV DT neutron generator for characterization and verification of spent nuclear fuel assemblies.

Many different nondestructive analysis techniques are currently being investigated as a part of the United States Department of Energy's Next Generation Safeguards Initiative (NGSI) seeking methods to quantify plutonium in spent fuel. Neutron Resonance Transmission Analysis (NRTA) is one of these techniques. Having first been explored in the mid-1970s for the analysis of individual spent-fuel pins a second look, using advanced simulation and modeling methods, is now underway to investigate the suitability of the NRTA technique for assaying complete spent nuclear fuel assemblies. The technique is similar to neutron time-of-flight methods used for cross-section determinations but operates over only the narrow 0.1-20 eV range where strong, distinguishable resonances exist for both the plutonium (239, 240, 241,242Pu) and uranium (235,236,238U) isotopes of interest in spent fuel. Additionally, in this energy range resonances exists for six important fission products (99Tc, 103Rh, 131Xe, 133Cs, 145Nd, and 152Sm) which provide additional information to support spent fuel plutonium assay determinations. Initial modeling shows excellent agreement with previously published experimental data for measurements of individual spent-fuel pins where plutonium assays were demonstrated to have a precision of 2-4%. Within the simulation and modeling analyses of this project scoping studies have explored fourteen different aspects of the technique including the neutron source, drift tube configurations, and gross neutron transmission as well as the impacts of fuel burn up, cooling time, and fission-product interferences. These results show that NRTA may be a very capable experimental technique for spent-fuel assay measurements. The results suggest sufficient transmission strength and signal differentiability is possible for assays through up to 8 pins. For an 8-pin assay (looking at an assembly diagonally), 64% of the pins in a typical 17? 17 array of a pressurized water reactor fuel assembly can be part of a complete transmission assay measurement with high precision. Analysis of rows with up to 12 pins may also be feasible but with diminished precision. Preliminary data analysis of an NRTA simulation has demonstrated the simplicity of the technique.

Neutron resonance transmission analysis (NRTA) is an active-interrogation nondestructive assay (NDA) technique capable of assaying spent nuclear fuel to determine plutonium content. Prior experimental work has definitively shown the technique capable of assaying plutonium isotope composition in spent-fuel pins to a precision of approximately 3%, with a spatial resolution of a few millimeters. As a Grand Challenge to investigate NDA options for assaying spent fuel assemblies (SFAs) in the commercial fuel cycle, Idaho National Laboratory has explored the feasibility of using NRTA to assay plutonium in a whole SFA. The goal is to achieve a Pu assay precision of 1%. The NRTA technique uses low-energy neutrons from 0.1-40 eV, at the bottom end of the actinide-resonance range, in a time-of-flight arrangement. Isotopic composition is determined by relating absorption of the incident neutrons to the macroscopic cross-section of the actinides of interest in the material, and then using this information to determine the areal density of the isotopes in the SFA. The neutrons used for NRTA are produced using a pulsed, accelerator-based neutron source. Distinguishable resonances exist for both the plutonium (239,240,241,242Pu) and uranium (235,236,238U) isotopes of interest in spent fuel. Additionally, in this energy range resonances exists for six important fission products (99Tc, 103Rh, 131Xe, 133Cs, 145Nd, and 152Sm) which provide additional information to support spent fuel plutonium assay determinations. Based on extensive modeling of the problem using Monte Carlo-based simulation codes, our preliminary results suggest that by rotating an SFA to acquire four symmetric views, sufficient neutron transmission can be achieved to assay a SFA. In this approach multiple scan information for the same pins may also be unfolded to potentially allow the determination of plutonium for sub-regions of the assembly. For a 17? 17 pressurized water reactor SFA, a simplistic preliminary analysis indicates the mass of 239Pu may be determined with a precision on the order of 5%, without the need for operator-supplied fuel information or operational histories. This paper will present our work to date on this topic, indicate our preliminary findings for a conceptual assay approach, discuss resilience against spoofing, and outline our future plans for evaluating the NRTA technique for SFA plutonium determination.