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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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All sourcesNASA NTRSDOE OSTI
DOE OSTI2016

Performance Criteria for Capture and/or Immobilization Technologies

The capture and subsequent immobilization of the four volatile radionuclides ( 3 H, 14 C, 85 Kr, and 129 I) from the off-gas streams of a used nuclear fuel reprocessing facility has been a topic of substantial research interest for the US DOE and international colleagues. Regulations set forth by the US EPA direct that some or all of these radionuclides (based upon fuel burnup, fuel type, cooling time, etc.) will require removal, to some extent, from the plant effluent streams prior to discharge to the environment. Upon removal, the radionuclide, as well as any associated sorbent, is destined for waste. Research of separation and capture methodologies has included a wide range of technologies including liquid caustic scrubbing systems, solid adsorbents, and cryogenic distillation. The studies of waste forms have been correspondingly diverse. In considering the technologies available for future development and implementation of both sorbents and waste forms, it will be necessary to use benchmarked measures of performance to objectively evaluate each sorbent system or waste form. This document is intended to provide initial guidance on the types of performance criteria for capture materials and waste forms intended for use in the recycling removal and disposal of UNF and, where possible, the minimum acceptable values for those criteria.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
DOE OSTI2014

Characterization of Used Nuclear Fuel with Multivariate Analysis for Process Monitoring

The Multi-Isotope Process (MIP) Monitor combines gamma spectroscopy and multivariate analysis to detect anomalies in various process streams in a nuclear fuel reprocessing system. Measured spectra are compared to models of nominal behavior at each measurement location to detect unexpected changes in system behavior. In order to improve the accuracy and specificity of process monitoring, fuel characterization may be used to more accurately train subsequent models in a full analysis scheme. This paper presents initial development of a reactor-type classifier that is used to select a reactor-specific partial least squares model to predict fuel burnup. Nuclide activities for prototypic used fuel samples were generated in ORIGEN-ARP and used to investigate techniques to characterize used nuclear fuel in terms of reactor type (pressurized or boiling water reactor) and burnup. A variety of reactor type classification algorithms, including k-nearest neighbors, linear and quadratic discriminant analyses, and support vector machines, were evaluated to differentiate used fuel from pressurized and boiling water reactors. Then, reactor type-specific partial least squares models were developed to predict the burnup of the fuel. Using these reactor type-specific models instead of a model trained for all light water reactors improved the accuracy of burnup predictions. The developed classification and prediction models were combined and applied to a large dataset that included eight fuel assembly designs, two of which were not used in training the models, and spanned the range of the initial 235U enrichment, cooling time, and burnup values expected of future commercial used fuel for reprocessing. Error rates were consistent across the range of considered enrichment, cooling time, and burnup values. Average absolute relative errors in burnup predictions for validation data both within and outside the training space were 0.0574% and 0.0597%, respectively. The errors seen in this work are artificially low, because the models were trained, optimized, and tested on simulated, noise-free data. However, these results indicate that the developed models may generalize well to new data and that the proposed approach constitutes a viable first step in developing a fuel characterization algorithm based on gamma spectra.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
DOE OSTI2023

A Review of Advanced Test Reactor Fuel and Assessment of Its Compatibility with the ZIRCEX Chlorination Process

Advanced Test Reactor (ATR) fuel has been identified as a resource for high-assay low-enriched uranium (HALEU) production. A survey was performed on the published literature describing ATR fuel. The geometry of the fuel is complex; different parts of the fuel compact experience differing neutron flux and burnup. The literature is sparse, and access is controlled. Therefore, fundamental studies of fuel reprocessing must use a model fuel that represents the main chemical and structural features. Advanced chlorination, or chlorination with sulfur-chlorine bearing reagents is being investigated as way to separate the fuel from metal matrix alloys. A UAl x alloy will be fabricated with x = 3, 4, and 5. The potential chlorination of individual UAl x intermetallics will be assessed in the advanced chlorination process of Al-8001 and Al-6061 as well as a representative mixture. Initial studies will track the alloying elements of the Al, which are Si, Fe, Cu, Mn, Mg, Cr, Zn, and Ti, in addition to the U itself. Further studies will include fission product simulants. Because advanced chlorination solvents include sulfur, the chemistry of sulfur with major and minor constituents will also be investigated. The experimental work accompanied by neutronic calculations will allow the assessment of the feasibility of advanced chlorination to separate aluminum from uranium. If bench-scale testing appears promising, then small-scale tests in shielded facilities with irradiated cladding, lightly irradiated fuel, and spent nuclear fuel are recommended to track the complete inventory of fissile actinides, fission product impurities, and reagent solids and liquids.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
NASA NTRS1975

The UF6 Breeder - A solution to the problems of nuclear power

One of the major advantages of uranium hexafluoride reactors for power generation is the simplified fuel reprocessing scheme which the gaseous fuel makes possible. Critical experiments related to the development of the reactors for electric power generation are discussed along with UF6 breeder reactor studies. Previous energy conversion studies are reported, taking into account gas turbine power plants, thermionic conversion, and MHD conversion. Thermodynamic cycle analyses show that high efficiencies can be achieved using UF6 as the working fluid for Rankine or Brayton cycles without requiring excessive temperatures.

Williams, J. R.↗
DOE OSTI2016

Near-Term Deployment Viability of Liquid-Fuel Molten Salt Reactors

Molten salt reactors (MSRs) with liquid fuel offer many benefits such as continuous fuel reprocessing, which provides unprecedented flexibility in fuel cycle selection, and excellent performance both in thermal efficiency and intrinsic safety. However, challenges such as the need for proliferation-resistant design and a high-temperature, corrosive environment for structural materials have hindered their development. New MSR concepts, such as the ThorCon Do-able Molten Salt Reactor, aim to simplify design and operation in order to cut costs and enable deployment in a relatively short period of time. The proposed methods for reducing the impact of longstanding issues on MSR deployment have incentivized further technical assessment of the reactor design. This study selectively examined the (1) thermal hydraulics, (2) neutronics, (3) primary safety systems, and (4) economics of a representative liquid-fuel MSR to better understand the technical and economic viability for near term deployment of this technology. (authors)

21 SPECIFIC NUCLEAR REACTORS AND ASSOCIATED PLANTS↗
DOE OSTI2019

Panel Session 32: Panel: Bringing First-of-a-Kind Treatment Facilities On-Line: Idaho IWTU Commissioning Approach (2/5)

This panel discussed the activities of bringing a first-of-a-kind treatment facility online: The Integrated Waste Treatment Unit (IWTU). The design was designed to treat 900,000 gallons of sodium-bearing liquid waste. Construction of this first-of-a-kind treatment facility was completed in 2012. A new approach was adopted in 2016 after multiple challenges were encountered during facility commissioning. This session focused on the Integrated Waste Treatment Unit (IWTU), which was constructed to convert the remaining 900,000 gallons of liquid sodium-bearing waste at the Idaho National Laboratory Site, Idaho, USA, to a granular solid. The liquid waste was generated during historic spent nuclear fuel reprocessing campaigns at the Idaho Nuclear Technology and Engineering Center and was transferred to three underground storage tanks. The waste was not first-cycle waste but was rather the liquid rinse waste from flushing waste transfer lines between reprocessing runs. IWTU will employ a steam-reforming process to treat the liquid waste. The resulting granular solid will be transferred to stainless steel canisters and then to concrete vaults, which will be stored on site until an off-site national geologic repository is available to accept the waste. Presentation proposed: Bringing First-of-a-Kind Treatment Facilities On-Line: Idaho IWTU Commissioning Approach (Joel Case, US DOE (USA), Leo Thompson, Sterling Engineering and Consulting Group, LLC (USA), Joseph Giebel, Fluor Idaho, LLC (USA), Richard Boardman, Idaho National Laboratory (USA), Kevin O'Neill, US DOE (USA))

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2019

Hanford Tank Side Cesium Removal System: Process Description and Performance Metrics - 19613

The Tank Side Cesium Removal (TSCR) System is a modular, quickly-deployable and passively safe system for efficiently removing solids and cesium from alkaline liquid waste raffinate created by spent fuel reprocessing on the Hanford site. It further describes TSCR component design features, system performance metrics and operational sequences used for liquid waste treatment, as well as spent ion exchange column (IXC) replacement and storage. This presentation should be of great interest to parties responsible for treatment and disposal of liquid waste containing high concentrations of cesium. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2020

A Dose Assessment Model for Radioactive Waste Exposed by Gully Erosion at West Valley - 20513

The Western New York Nuclear Service Center (WNYNSC), located approximately 48 km south of Buffalo, New York, is the site of a former nuclear fuel reprocessing and radioactive waste disposal facility. Spent nuclear fuel was processed there from 1966 to 1972, leaving behind radioactive and chemical wastes in two disposal areas and a waste tank farm. Site operations also resulted in releases of radioactivity to site soils, groundwater, and to surface waters draining the site. The New York State Energy Research and Development Authority (NYSERDA) and the U.S. Department of Energy (DOE) are collaborating in a process of decision making for decommissioning those facilities remaining at the WNYNSC following the completion of Phase 1 decommissioning. Neptune and Company, Inc. (Neptune) was contracted to develop a probabilistic performance assessment (PPA) computer model to assist the agencies in this process. The PPA Model includes a contaminant transport component focusing on the movement of contaminants within and among environmental media including groundwater and surface water transport, contaminant translocation by plants and animals, diffusion, and erosion. The model also includes evaluation of potential exposure and health effects for a Resident Farmer exposure scenario, where the Resident Farmer represents a critical group, described as that group of individuals reasonably expected to receive the greatest exposure to residual radioactivity for any applicable set of circumstances. The West Valley Site is located in the glaciated Allegheny Plateau region of western New York State. The waste reprocessing and disposal areas were constructed on a relatively fat area of plateau dissected by drainages of Buttermilk Creek, including Erdman Brook, Franks Creek, and Quarry Creek. An important aspect of the contaminant transport component of the PPA model is consideration of erosive processes such as slumping of the stream slopes and the advance of gullies from these streams. These erosion processes remove material from the plateau, growing the size of the creek valleys and making them wider and deeper. Of particular interest for the impact of erosion is radioactive waste contained in the Nuclear Regulatory Commission (NRC)-Licensed Disposal Area (NDA), the New York State-Licensed Disposal Area (SDA), and residual radiological inventory in the underground storage tanks at the Waste Tank Farm (WTF). The PPA Model is organized around geographically-defined facilities which were constructed upon the plateau, including the NDA, SDA, and WTF. Ongoing stream erosion processes will potentially transfer radioactive waste and residual inventory from these facilities to the ground surface on adjacent hillslope areas where erosion has breached the facility. Hence, it is important to evaluate the consequences of potential exposures to a Resident Farmer on the hillslopes below a breached facility. Two interrelated aspects of the dose assessment model related to hillslope exposure are discussed: 1) representation of the physical processes related to transport of radionuclides from facilities onto the hillslopes, and from the hillslopes into adjoining creeks where contaminated material migrates downstream with surface water and sediment, and; 2) adaptation of the activities associated with the Resident Farmer scenario to assess potential exposures to contamination in the hillslope areas. This discussion will cover the conceptual basis of the hillslope exposure and transport models, and also implementation in the PPA computer model. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2015

The German product quality control of the compacted metallic nuclear waste - 15311

The treatment and safe disposal of spent nuclear fuel is a key challenge of nuclear energy utilization and has to be accomplished regardless the future nuclear of electricity production or phase-out policies. Until June 2005 approx. 6662 tons of spent fuel from German nuclear power plants was sent to the La Hague (France) and Sellafield (UK) plants for reprocessing. An equivalent amount of nuclear waste compounds has contractually to be returned to Germany, which is currently in progress. The returnable waste streams comprise mainly highly-active vitrified waste containing a major part of fission products and actinides, and intermediate-active super-compacted metallic waste containing reprocessed fuel element's structural materials and some technological waste from the reprocessing process itself. Shearing and dissolution of spent fuel leaves scraps of fuel metal cladding, the end-pieces and spacers which are contaminated, activated and irradiating from their life in a reactor core. In fact, this metallic intermediate level radioactive waste makes up a bit more than half of the total volume of the reprocessed waste. At La Hague the metallic waste is super-compacted. Several, typically eight, compacted discs are stacked in a stainless steel container, named CSD-C as for 'Colis Standard de Dechets Compactes'. 4104 containers of such CSD-Cs in 152 transport/storages casks have to be returned to Germany. Each one of them has to be checked and quality certified for its conformity with German national product specifications and acceptance criteria by independent national product quality control inspectors (PKS). The residue package documentation has to be complete and the characterization methods have to be comprehensive. Due to the heterogeneity of metallic waste the characterization and control of its properties is very complex. The nuclear characterization is performed by means of non-destructive measurements, where only a few key nuclides are measured directly. In fact, the proper calculation of the whole nuclear inventory relies on numerous supplementary simulations. The measurement and calculation methodology is scrutinized by PKS in detail and key points are benchmarked with our own simulations for the sake of an independent nuclear inventory declaration check. With respect to the vast amount of documentation and parameters, which have to be checked and verified, PKS had to optimize their checking procedures. For this purpose dedicated proof tools have been developed that shall be applied for selected indicative cross-checks of the relevant parameters. This contribution is dedicated to the procedure of quality control by PKS and examples of actually performed computational verifications of declared nuclear inventory. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2022

The Role of Pulse Radiolysis in Advanced Nuclear Fuel Cycles

The effects of ionizing radiation are ubiquitous throughout all aspects of a nuclear fuel cycle. The complexity and intensity of these effects are greatest during reactor operations and in the management of used nuclear fuel and waste. Radiation-induced processes typically promote the chemical transformation of molecules and materials with the formation of potentially detrimental degradation products and corresponding changes in physical and chemical properties, which ultimately impact the effectiveness and longevity of nuclear technologies. Consequently, a molecular-level understanding of radiation effects over multiple time, distance, and material domains is essential for the innovation and deployment of next generation nuclear technologies. Attaining this knowledge necessitates a firm grasp of radiation-induced reaction kinetics, for which pulsed electron radiolysis is the methodology of choice. Presented here are several recent studies from our group that demonstrate the critical role of pulsed electron radiolysis techniques in the advancement of our understanding of radiation-induced chemistry under advanced nuclear fuel cycle conditions. Research topics include late actinide redox chemistry, radiation robustness of used nuclear fuel reprocessing complexants, and the behavior of metal cations in high temperature molten salt media.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗
DOE OSTI2024

Backend Nuclear Fuel Cycle Radiation Chemistry

Given global commitments to significantly increase nuclear energy capacity, it is now more important than ever to develop efficient used nuclear fuel management strategies to improve resource utilization, energy security, and waste minimization. Here, an overview of nuclear energy, backend fuel cycle challenges, and advances in used nuclear fuel reprocessing radiation chemistry will be presented. More specifically, the use of electron pulse irradiation techniques to explore radiation-induced reaction mechanisms in actinide containing solutions and solvent systems.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗
DOE OSTI2015

Overcoming challenges in delivering 5 Avantech water treatment systems at Fukushima - 15544

The Great East Japan Earthquake has left the Fukushima Daiichi Nuclear Station with many challenges related to water treatment. This paper will provide information on three systems provided for the treatment of [1] accumulated water associated with the Circulated Water Cooling System, [2] sub-drain water removed from wells adjacent to the Unit 1-4 Reactor and Turbine Buildings, and [3] wash water from decontamination of vehicles and equipment. Specific information will be presented on work that was completed to overcome process, installation and logistical challenges associated with these water streams including the following: - Selection of technology and equipment for removal of specific radionuclides - Performance results of highly selective adsorbents used for removing radionuclides in the presence of varying concentrations of chlorides and other natural constituents - Description of process flowsheets and equipment configuration - Discussion of the post-accident work environment and the related work site restrictions Results show that the customized solutions will enable the utility to clean-up the wastewater for cooling, reuse and potential discharge. The technologies used for the three water treatment systems are directly applicable to the treatment of similarly challenging water streams at commercial nuclear power plants, fuel reprocessing plants and governmental nuclear facilities worldwide. The use of these technologies will aid in the lowering of radioactivity released to the environment, worker radiation exposure and the amount of secondary waste requiring long term storage and/ or disposal. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2015

Methods for radiological assessment of C-14 in air effluents - 15419

The purpose of this paper is to report on methods used for the assessment of -dose significant- C-14 being discharged into the air from nuclear facilities. GEL laboratories, LLC and GEL Engineering LLC, (GEL) undertook the task of developing new and improved methods to better identify the release of C-14 in the various chemical forms released from nuclear reactors and fuel reprocessing facilities. To completely understand the environmental releases and impact to the public a two-step approach was selected. The first step was to develop a sampling method that would enable an accurate assessment of the ratio of C-14 discharged as carbon dioxide compared to organic gases like methane. This is very important to dose modeling calculations to members of the public. Once this ratio was understood, the second step was to develop a method to track inorganic forms of C-14 with standard environmental air monitoring equipment and achieve a detection limit that was in line with NRC 10CFR Appendix I dose modeling requirements. GEL development efforts focused on using a solid sample cartridge that would fit into standard air sampling equipment used at nuclear plants. The cartridge and sorbent needed to be capable of running 7 days at 24 hours per day and not saturate with stable carbon dioxide. The process developed for analyzing the sorbent involves chemically removing the carbon dioxide and ultimately counting by liquid scintillation counting. The method yields a detection limit for C-14 of 0.02 Bq/m{sup 3} which provides a dose calculation of approximately 0.1 mSv/yr when applied to the child model. This paper will describe the methods and results used to determine field environmental monitoring for C-14 using GEL cartridges also known as -GELsorb C14-. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2015

FY-2015 Methyl Iodide Deep-Bed Adsorption Test Report

Nuclear fission produces fission and activation products, including iodine-129, which could evolve into used fuel reprocessing facility off-gas systems, and could require off-gas control to limit air emissions to levels within acceptable emission limits. Deep-bed methyl iodide adsorption testing has continued in Fiscal Year 2015 according to a multi-laboratory methyl iodide adsorption test plan. Updates to the deep-bed test system have also been performed to enable the inclusion of evaporated HNO 3 and increased NO 2 concentrations in future tests. This report summarizes the result of those activities. Test results showed that iodine adsorption from gaseous methyl iodide using reduced silver zeolite (AgZ) resulted in initial iodine decontamination factors (DFs, ratios of uncontrolled and controlled total iodine levels) under 1,000 for the conditions of the long-duration test performed this year (45 ppm CH3I, 1,000 ppm each NO and NO 2 , very low H 2 O levels [3 ppm] in balance air). The mass transfer zone depth exceeded the cumulative 5-inch depth of 4 bed segments, which is deeper than the 2-4 inch depth estimated for the mass transfer zone for adsorbing I 2 using AgZ in prior deep-bed tests. The maximum iodine adsorption capacity for the AgZ under the conditions of this test was 6.2% (6.2 g adsorbed I per 100 g sorbent). The maximum Ag utilization was 51%. Additional deep-bed testing and analyses are recommended to (a) expand the data base for methyl iodide adsorption and (b) provide more data for evaluating organic iodide reactions and reaction byproducts for different potential adsorption conditions.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
DOE OSTI2017

Aging Processes of Silver Mordenite and Silver Functionalized Aerogel in Dry Air, Humid Air and NO/N{sub 2}

One major problem in the treatment of nuclear-fuel reprocessing off-gas streams is the loss of capacity of the adsorbents exposed to off-gas streams containing air, I{sub 2} vapor, H{sub 2}O vapor, NO and NO{sub 2} over extended periods of time. These aging processes decrease the adsorption capacity of the reduced silver exchanged mordenite (Ag{sup 0}Z) and silver functionalized silica aerogel (Ag{sup 0}-aerogel) columns during the long processing time of iodine adsorption. Significant work has been performed over the past few years at ORNL on Ag{sup 0}Z and Ag{sup 0}-aerogel aging. The Ag{sup 0}Z and Ag{sup 0}-aerogel were aged in 4 different gas streams at 150 deg. C for periods of time up to 6 months. The aging samples were then loaded with I{sub 2} to determine the capacity loss after the aging. The results are summaries in Tab. 1. It was found that both Ag{sup 0}Z and Ag{sup 0}-aerogel had different amounts of capacity loss in different gases. For example, 40% and 22% capacity loss were observed for Ag{sup 0}Z and Ag{sup 0}-aerogel when aged in dry air for 6 months, while 78% and 43% capacity loss were observed when aged in 1% NO{sub 1} for 2 months. In addition, it was found that Ag{sup 0}Z and Ag{sup 0}-aerogel had a different capacity loss when aged at the same conditions. For example, after aged in 2% NO{sub 2} for 2 months, Ag{sup 0}Z lost 30% iodine capacity, but there was no capacity loss for Ag{sup 0}- aerogel. The differences in capacity loss should be due to different aging processes occurred when Ag{sup 0}Z and Ag{sup 0}- aerogel were exposed to different gases. The mechanisms of the aging processes have not been determined and need to be studied with proper chemical and physical characterization methods. Towards this objective, experimental work is proposed and on-going to obtain data to determine the mechanisms of the aging processes of Ag{sup 0}Z and Ag{sup 0}-aerogel in different aging gas streams. In addition, models will be developed to describe the deactivation process of the adsorbents when exposed to off gases. The deactivation model will be included in the transport models for predicting the adsorption processes over these long-time periods.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
DOE OSTI2017

{sup 14}C Entry into the Atmosphere

{sup 14}C enters the atmosphere in amounts equivalent to 1.4 PBq/yr with total accumulation 140 PBq via cosmic radiation. As a result of nuclear explosions (1950–1969), its activity in the atmosphere exceeded 200 PBq. At present, {sup 14}C has been completely removed into bottom waters and sedimentary rocks in the ocean. The activity of the {sup 14}C entering the atmosphere from all operating nuclear reactors equals ~0.3 PBq/yr and the amount from all spent fuel reprocessing facilities equals ~0.06 PBq/yr. The admissible levels of {sup 14}C emissions must not exceed levels corresponding to peroral intake dose 10 μSv/yr. This is can be accomplished by means of a system of measures: reduction of the volume of technogenic gases and their {sup 12}CO{sub 2} content, combining high-efficiency purification with dispersion through high exhaust-stacks, and developing new technologies and reagents binding {sup 14}C in compact forms.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗
DOE OSTI2025

Field Testing of Safeguards Technologies in the Hot Fuel Examination Facility

Recent developments in nuclear fuel reprocessing techniques have yielded more efficient processes and fuel cycle options that strengthen the nuclear industry and production of clean energy. One such area of interest is pyroprocessing of used oxide fuel. However, with these advances in the back end of the nuclear fuel cycle, advances in safeguards instrumentation, measurements, and approaches are needed to ensure special nuclear material (SNM) is accounted for according to regulatory requirements. As a high-level overview of a nominal pyroprocessing approach, used oxide fuel from commercial light water reactors (LWR) is mechanically removed from the metallic cladding. Then the fuel is crushed and randomized representative samples are taken and sent to an analytical lab for analysis. The analytical results of the feed material are used for input accountancy into the rest of the process. The crushed oxide fuel is then moved to the oxide reduction (OR) furnace where it is reduced from an oxide to metallic form. The OR product is distilled to remove salt and then moved to an electrorefiner (ER), where it is immersed in a eutectic mixture of lithium chloride potassium chloride (LiCl-KCl) that typically ranges between 450-550 ?. Within the ER, the usable uranium is electrochemically transported through the molten salt from the anode to the cathode, and then subsequently removed as a relatively pure U product.. A simplified model of pyroprocessing techniques with added emphasis on the safeguards can be seen below in Fig. 1

11 - NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
DOE OSTI2026

INL Intern Poster Session

Characterization of off-gas constituents from nuclear fuel reprocessing can be measured using a residual gas analyzer. Characterization of this off-gas is important in a closed fuel cycle, where gasses such as Nox, Kr, I, and C-14 need to be removed from reprocessing plants to meet regulatory requirements. Both Kr and Xe have low chemical reactivity, making capture and separation difficult. Solid sorbents can be used to capture these gases as an alternative to cryogenic distillation, which is energy intensive and hazardous. AgZ-PAN and HZ-PAN are two solid sorbents that have demonstrated selective capture of Xe and Kr. A residual gas analyzer can be used to obtain breakthrough curves that demonstrate how well this adsorption and separation occur. The breakthrough curve is dependent on packing density, column size, and flow rate. Data obtained from the RGA was verified with a gas chromatographer.

11 - NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗