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At least 361 records · Page 20
All sourcesNASA NTRSDOE OSTI
DOE OSTI2012

Report of the Fuel Cycle Research and Development Subcommittee of the Nuclear Energy Advisory Committee

The Fuel Cycle (FC) Subcommittee of NEAC met February 7-8, 2012 in Washington (Drs. Hoffmann and Juzaitis were unable to attend). While the meeting was originally scheduled to occur after the submission of the President’s FY 2013 budget, the submission was delayed a week; thus, we could have no discussion on balance in the NE program. The Agenda is attached as Appendix A. The main focus of the meeting was on accident tolerant fuels, an important post Fukushima issue, and on issues related to the report of the Blue Ribbon Commission on America’s Nuclear Future (BRC) as related to the responsibility for used fuel disposal which was assigned to the FC program with the end of the Office of Civilian Radioactive Waste Management. In addition we heard an update on the systems study program which is aimed at helping chose the best options for advanced reactors, and possible new study on separation and waste form relevance to used fuel disposal (these two items are only discussed in this section of the report).

Fuel Cycle, NEAC, accident tolerance, used fuel di↗
DOE OSTI2013

Why reconsider the thorium fuel cycle?

In this paper we have endeavored to present the available technical information on the potential use of Th in nuclear fuel cycle (FC) applications as compared to U without subjective evaluations. Where helpful, we have compared the technical attributes of Th-232 as a fertile isotope and U-233 as a fissile isotope with other similar isotopes (i.e., U-238, and U-235 and Pu-239, respectively). In addition, we have summarized (a) experience gained to-date with fabricating and reprocessing of Th-232/U-233 fuels, (b) factors concerning Th fuel irradiation in both test reactors and power reactors, and (c) differences in the backend of the FC with emphasis on repository risks. As might be expected, many technical aspects of Th vs. U have not changed since the sixties. However, there are some factors elaborated in this paper that have changed. Changes potentially encouraging Th use are: (a) the ability to recover large amounts of Th as a byproduct with small attendant costs and environmental impacts, (b) the potential to produce fewer minor actinides (MA) and less Pu during power production, and (c) increased concerns about proliferation which might be somewhat mitigated by the high radioactivity and amenability to isotopic dilution of U-233. Changes challenging Th utilization are: (a) obtaining sufficient experience handling Th/U-233 fuels, (b) the existence of large inventories of depleted U and continuing discovery of large U resources, and (c) recognition that the extent to which U-233 might mitigate proliferation concerns is not as large as originally hoped.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
DOE OSTI2017

Test facility for fission chamber assemblies - 239

The Institution -Project Center ITER- with participation of the National Research Nuclear University MEPhI are developing the neutron diagnostics -Divertor Neutron Flux Monitor- (DNFM) for the International Thermonuclear Experimental Reactor (ITER). This diagnostics shall ensure measurement of the total neutron yield and ITER fusion power. Assemblies of fission chambers (FC) with different fissile materials and sensitivities are planned to be used for the neutron flux measurement. Study of fission chambers characteristics and acceptance testing of the diagnostic system will be carried out at the testing facility of the neutronic laboratory of the 'TRINITI' Institute. The facility includes: compact powerful neutron generator with the power, control and monitoring system; remote handling system for FCs positioning and movement; novel three channels data acquisition and processing system. Each acquisition channel contains some measuring circuits with signal processing. This set of circuits provides neutron flux measurement in the range of at least 10 decades for each single FC. Data acquisition and processing system features are: signal digitizing with sample rate up to 125 MHz; real time data processing with computation and data update cycle from 0.1 ms. This paper examines the structure, composition and specification of the test facility. Application software, hardware solutions and the results of fission chambers prototypes tests are discussed. (authors)

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2016

Evaluating Age Effects on HEPA Filter Performance

Nuclear grade high efficiency particulate air (HEPA) filters are routinely employed as the final control element in confinement ventilation systems. The traditional HEPA filter utilizes a pleated filter medium of fibrous glass that has been produced in a manner analogous to manufacturing paper. These filters are the physically weakest element in a containment ventilation system. Containment ventilation systems are designed to condition the air-stream (temperature, relative humidity, moisture, particle size distribution of aerosols, and aerosol concentration) to levels/conditions that fibrous glass HEPA filters can handle. Approximately 6000 nuclear grade HEPA filters are purchased each year for use in the DOE/NNSA complex. Additional filters are purchased for use in commercial nuclear power generation and ventilation systems of other nuclear applications. These filters are designed and tested in accordance with the American Society of Mechanical Engineers (ASME) AG-1 Code Nuclear Air and Gas Treatment. This code establishes design requirements and qualification procedures. Qualification testing of axial flow filters is described in paragraphs 5000 and following of AG-1. The series of qualification tests are intended to describe the operating envelope of HEPA filters and verify the reliability of a filter design. AG-1 qualification also confirms the pedigree of components used in manufacture for that filter design. The collective set of qualification tests establishes the assumed operating envelope for AG-1 filters. The effects of age on HEPA filter performance have been a concern for at least two decades. A combination of physical evaluation of aged filter media and a review of filter failure records resulted in Appendix C of the Nuclear Air Cleaning Handbook (NACH), Determination of HEPA Filter Life. This states that HEPA filters are not to be used beyond 10 years from the date of manufacture. Additionally, filters put into service in locations where they may become wet are to be taken out of service five years from date of manufacture. Filters that have become wet are to be taken out of service immediately. Finally, it should also be pointed out that filters held in Level B storage are subject to the same 10-year service life. Very limited bench-scale testing in the 1990's raised concern that aging HEPA filters do not have the strength to withstand an accident scenario. In May of 1999, the DNFSB released a Technical Report 23 entitled HEPA Filters Used in the Department of Energy's Hazardous Facilities. This report expressed concerns for the potential vulnerability of HEPA filters in vital safety systems. Concerns and uncertainty associated with degradation of HEPA filter performance over time led the DOE sites to limit HEPA filter service life to 10 years from the date of manufacture or five years in cases where filters may become wet. Establishment of a conservative service life needs to be based on data from a structured series of tests comparing the performance envelope of new and aged full-scale filters. A service life that is insufficiently conservative endangers workers and the public. One that is excessively conservative costs can cause hundreds of otherwise unnecessary filter changes. This increases exposure of employees, disrupts facility operations, and increase disposal costs by millions of dollars annually. Conclusive data are needed to resolve uncertainty associated with the damaging effects of aging on durability of HEPA filters. Therefore, this study needs to provide a sufficient body of evidence to allow DOE and site professionals to make prudent decisions. An updated version of ASME AG-1 Section FC included a non-mandatory appendix that would include the DOE guidance for service life of HEPA filters. Balloting of this revision generated significant resistance to inclusion of any kind of service life language citing the lack of supporting experimental data. Efforts to resolve negative votes failed and resistance to acceptance of the language increased. The result has been to not include service language in Section FC and requests to remove it from sections that already include such language. The recent activity of the ASME AG-1 Committee on Nuclear Air and Gas Treatment effectively de-emphasizes following DoE's service life guidelines. The DOE Office of Nuclear Safety under its NSR and D program provided the Mississippi State University Institute for Clean Energy Technology (ICET) finding to initiate a study to determine the effects of aging on AG-1 axial flow filters just prior to actions taken within the AG-1 committee regarding service life. The NSR and D funding facilitated timely development of a national technical working group comprised of members from the regulatory community, DOE complex, and commercial power to resolve uncertainty associated with effects of aging. The Department of Energy Office of Environmental Management (DOE-EM) has been funding the ICET to evaluate the performance envelope for AG-1 HEPA filters. ICET is one of DOE-EM's qualified suppliers. Synergy has been achieved by associating the NSR and D aged filter activities to testing activities evaluating the performance envelopes of separator and separator-less AG-1 HEPA filters funded by DOE-EM. The DOE-EM funded activities establish baseline data for the aged filter study and future EM funding will provide long term support for testing additional aged filters. EM funding of new filters includes analytical evaluation of media tensile strength by thermal analysis to establish baseline values and determine mass loss of moisture resistance and acrylic binders due to use. All of these values can be used for comparison of test results for aged filters. (authors)

07 ISOTOPE AND RADIATION SOURCES↗
DOE OSTI2025

CMI Winter Meeting 2025 Presentation

Lanthanides are important to many technologies including magnets used in high efficiency traction motors. While common in the environment and industrial waste streams, lanthanides are often present at very low concentrations. This work demonstrates synergistic lanthanide recovery from an aqueous magnet leachate to single ppm concentrations using Na2SO4 addition and subsequent DME-FC treatment. It was found that combining DME-FC with low concentrations of Na2SO4 (~0.1 M) results in synergistic isolation of lanthanides while making use of Na2SO4, an excessive byproduct of hydrometallurgical metal production. Combined Na2SO4 + DME reduced lanthanide metal ion's (Pr, Nd, Sm, Gd, Dy, and Ho) solubilities by 1,000 - 25,000x with final concentrations ranging from 2 ppm to 200 ppm. This can be compared to 0.1 M Na2SO4 alone providing a 10 - 200x reduction and DME providing a 100 - 1,500x reduction in lanthanide solubilities. Final solution concentrations of lanthanides were 99.8% lower than what could not be achieved with either individual process. The results also reveal different periodic trends in the solubility reduction for DME and Na2SO4.

37 - INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL C↗
DOE OSTI2019

Electrocatalytic CO 2 Reduction with a Ruthenium Catalyst in Solution and on Nanocrystalline TiO 2

A Ru II complex [Ru(PO 3 Et 2 -ph-tpy)(6-mbpy)(NCCH 3 )] 2+ [PO 3 Et 2 -ph-tpy=diethyl(4-[(2,2':6',2"-terpyridin)-4'-yl]phenyl)phosphonate; 6-mbpy=6-methyl-2,2'-bipyridine] is explored as a molecular catalyst for electrocatalytic CO 2 reduction in both a homogeneous solution and, as a phosphonated derivative, on nanocrystalline-TiO 2 surfaces. In CH 3 CN, the complex acts as a selective electrocatalyst for reduction of CO 2 to CO at a low overpotential of 340 mV but with a limited turnover number (TON). An enhancement in reactivity was observed by immobilizing the phosphonated derivative of the catalyst on a nanocrystalline-TiO 2 electrode surface, with the catalyst surface protected by a thin overlayer of NiO. The surface-functionalized electrode was characterized by X-ray photoelectron and diffuse reflectance spectroscopies (XPS and DRS). Electrocatalytic reduction of CO 2 to CO occurred at -1.65 V versus Fc +/0 with a TON of 237 per catalyst site during 4 h of electrocatalysis. Post-catalysis XPS measurements reveal that the molecular structure of the catalyst is retained on TiO 2 after the long-term electrocatalysis.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2018

Multielectron Redox Chemistry of Transition Metal Complexes Supported by a Non-Innocent N 3 P 2 Ligand: Synthesis, Characterization, and Catalytic Properties

A new redox-active, diarylamido-based ligand (L N3P2 ) capable of κ 5 -N,N,N,P,P chelation has been used to prepare a series of complexes with the general formula [M II (L N3P2 )]X, where M = Fe (1; X = OTf), Co (2; X = ClO 4 ), or Ni (3; X = ClO 4 ). The diarylamido core of monoanionic L N3P2 is derived from bis(2-amino-4-methylphenyl)amine, which undergoes condensation with two equivalents of 2-(diphenylphosphanyl)benzaldehyde to provide chelating arms with both arylphosphine and imine donors. X-ray structural, magnetic, and spectroscopic studies indicate that the N 3 P 2 coordination environment generally promotes low-spin configurations. Three quasi-reversible redox couples between +1.0 and –1.5 V (vs. Fc + /Fc) were observed in voltammetric studies of each complex, corresponding to M II /M III oxidation, L N3P2 -based oxidation, and MII/MI reduction (in order of highest to lowest potential). Spectroscopic and computational analyses of 3 ox – generated via chemical one-electron oxidation of 3 – revealed that a stable diarylaminyl radical (L N3P2· ) is formed upon oxidation. The ability of the Co II complex (2) to function as an electrocatalyst for H 2 generation was evaluated in the presence of weak acids. Moderate activity was observed using 4-tert-butylphenol as the proton source at potentials below –2.0 V. The insights gained here will assist in the future design of pentadentate mixed N/P-based chelates for catalytic processes.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2010

Effect of Creep of Ferritic Interconnect on Long-Term Performance of Solid Oxide Fuel Cell Stacks

High-temperature ferritic alloys are potential candidates as interconnect (IC) materials and spacers due to their low cost and coefficient of thermal expansion (CTE) compatibility with other components for most of the solid oxide fuel cells (SOFCs) . However, creep deformation becomes relevant for a material when the operating temperature exceeds or even is less than half of its melting temperature (in degrees of Kelvin). The operating temperatures for most of the SOFCs under development are around 1,073 K. With around 1,800 K of the melting temperature for most stainless steel, possible creep deformation of ferritic IC under the typical cell operating temperature should not be neglected. In this paper, the effects of IC creep behavior on stack geometry change and the stress redistribution of different cell components are predicted and summarized. The goal of the study is to investigate the performance of the fuel cell stack by obtaining the changes in fuel- and air-channel geometry due to creep of the ferritic stainless steel IC, therefore indicating possible changes in SOFC performance under long-term operations. The ferritic IC creep model was incorporated into software SOFC-MP and Mentat-FC, and finite element analyses were performed to quantify the deformed configuration of the SOFC stack under the long-term steady-state operating temperature. It was found that the creep behavior of the ferritic stainless steel IC contributes to narrowing of both the fuel- and the air-flow channels. In addition, stress re-distribution of the cell components suggests the need for a compliant sealing material that also relaxes at operating temperature.

SOFC. creep, ferritic interconnects, long-term per↗
DOE OSTI2022

Parked aeroelastic field rotor response for a 20% scaled demonstrator of a 13‐MW downwind turbine

Abstract Aeroelastic parked testing of a unique downwind two‐bladed subscale rotor was completed to characterize the response of an extreme‐scale 13‐MW turbine in high‐wind parked conditions. A 20% geometric scaling was used resulting in scaled 20‐m‐long blades, whose structural and stiffness properties were designed using aeroelastic scaling to replicate the nondimensional structural aeroelastic deflections and dynamics that would occur for a lightweight, downwind 13‐MW rotor. The subscale rotor was mounted and field tested on the two‐bladed Controls Advanced Research Turbine (CART2) at the National Renewable Energy Laboratory's Flatiron Campus (NREL FC). The parked testing of these highly flexible blades included both pitch‐to‐run and pitch‐to‐feather configurations with the blades in the horizontal braked orientation. The collected experimental data includes the unsteady flapwise root bending moments and tip deflections as a function of inflow wind conditions. The bending moments are based on strain gauges located in the root section, whereas the tip deflections are captured by a video camera on the hub of the turbine pointed toward the tip of the blade. The experimental results are compared against computational predictions generated by FAST, a wind turbine simulation software, for the subscale and full‐scale models with consistent unsteady wind fields. FAST reasonably predicted the bending moments and deflections of the experimental data in terms of both the mean and standard deviations. These results demonstrate the efficacy of the first such aeroelastically scaled turbine test and demonstrate that a highly flexible lightweight downwind coned rotor can be designed to withstand extreme loads in parked conditions.

17 WIND ENERGY↗
DOE OSTI2018

Exchange Bias Effect in FeCo Nanoparticles

The exchange bias fields in FeCo nanoparticles are investigated. A series of Fe{sub 1−x}Co{sub x} ( x =0.3, 0.5, and 0.7) NPs were fabricated using the hydrothermal method. XRD studies determined that the structures of the first two NPs were body-centered cubic (BCC) while that of the third was of a disordered structure having a few small disordered BCC crystallites. SEM images of the first two showed that these nanocrystals have well-structured pyramid shapes with planar surfaces on them. FC and ZFC magnetization curves showed the temperature dependences of the magnetization of the first two FeCo NPs were different from that of the third FeCo NPs. The hysteresis loops measured at 300, 150, and 10 K showed horizontal shifts of several of the loops. The exchange bias fields at 10 K of the three FeCo NPs were small but in two of them, the Fe{sub 0.7}Co{sub 0.3} and the Fe{sub 0.3}Co{sub 0.7} NPs, the fields were large at 150 K. The exchange bas field in the first NPs remained large as the temperature was raised to 300 K. H{sub E} for the last FeCo NPs became small again at 300 K.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2018

Structure and Magnetization of Polycrystalline La{sub 0.66}Ca{sub 0.33}MnO{sub 3} and La{sub 0.66}Ba{sub 0.33}MnO{sub 3} Films Prepared Using Sol-Gel Technique

The structure and static magnetization of polycrystalline La{sub 0.66}Ca{sub 0.33}MnO{sub 3} (LCMO) and La{sub 0.66}Ba{sub 0.33}MnO{sub 3} (LBMO) films grown on glass substrate using sol-gel technique have been investigated. X-ray diffraction (XRD) analysis revealed the average grain sizes of about 12 and 10 nm for granular LCMO and LBMO samples, respectively. The root mean square (RMS) surface roughness of about 100 nm has been obtained for both films by using scanning electron microscope (SEM) technique. The temperature dependences of the magnetization of LCMO and LBMO films registered in zero field cooling (ZFC) and field cooling (FC) regimes revealed a superparamagnetic state in both samples with remarkable distribution of blocking temperatures in a wide temperature interval, the average values of which have been estimated to be about 120 and 90 K for LCMO and LBMO, respectively. The average magnetic crystallite sizes obtained from the magnetizations studies coincide with the values revealed from the structural studies.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2019

Preparation and Thermophysical Investigations of CoFe{sub 2}O{sub 4}-based Nanofluid: a Potential Heat Transfer Agent

Cobalt ferrite nanoparticles were synthesized by employing chemical co-precipitation technique. The structure, morphology, elemental composition, and magnetization studies of cobalt ferrite nanoparticles were carried by XRD, FE-SEM, EDS, and VSM techniques, respectively. Rietveld refined XRD pattern exhibited the single-phase cubic spinel structure with Fd-3m space group. FE-SEM images indicated some agglomeration of spherical grains which can be attributed to high surface energy and magnetic interactions. Presence of peaks of respective elements (Co, Fe, and O) in EDS spectrum showed formation of CoFe{sub 2}O{sub 4}. The M–H loop recorded at 300 K revealed superparamagnetic behavior and explained by fine particles size. The blocking temperature of the CoFe{sub 2}O{sub 4}nanoparticles from FC-ZFC curve was found to be 144 K. Cobalt ferrite–ethylene glycol nanofluids of various concentrations 0.0–1.0% in steps of 0.2% were prepared by ultrasonically assisted two-step technique. Thermophysical parameters such as thermal conductivity, specific heat, viscosity, and density were investigated as a function of both volume fraction and temperature. The experimental and theoretical value of each sample was correlated. The thermal conductivity was significantly enhanced with an increase in volume fraction and temperature.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Enhanced Magnetic Levitation and Guidance Force in MgB{sub 2} Bulks by Synthetic Engine Oil Immersion

We have used ‘Synthetic engine oil’ as a rich easily accessible carbon source and investigated the effect of engine oil on the microstructure, critical current density (J{sub c}), vertical levitation force (F{sub z}) and guidance force (F{sub x}) properties of MgB{sub 2} superconductor. The polycrystalline disk-shaped MgB{sub 2} bulk samples have been prepared using two-step solid-state reaction process. After the first heating process, MgB{sub 2} bulk samples immersed in the engine oil for different durations (30, 120, 300 and 1440 min). XRD analysis indicated the decreasing of lattice parameters of samples and confirmed C substitution in boron sites. Vertical levitation and guidance force measurements were carried out with both Field-cooling (FC) and zero-field-cooling (ZFC) regimes at different temperatures of 20, 24 and 28 K. It was found that engine oil addition slightly increases the levitation and guidance force properties. The F{sub z} values were obtained as 11.17 and 11.58 N for pure and MgB{sub 2} sample immersed for 30 min at 20 K in ZFC regime. In addition, the MgB{sub 2} sample immersed for 300 min in engine oil showed the highest J{sub c} value of 5.3×10{sup 4} A cm{sup − 2} at 15 K and self-field and showed the highest guidance force value of 4.14 N at 20 K. These finding suggest that synthetic engine oil is a cost-effective and promising method to improve the levitation and guidance force performance as well as the critical current density of MgB{sub 2} bulk superconductor.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2019

Magnetic Properties of Mn-Substituted Zn–Mg- and Zn–Co-Nanosized Compounds

Mn-substituted Zn–Mg and Zn–Co with chemical formula Mn{sub 0.3}Mg{sub 0.2}TM{sub 0.5}Fe{sub 2}O{sub 4} (TM = Zn or Co) fine powders have been synthesized by glycol-thermal process. XRD results reveal the formation of a cubic phase without any impurity phases. TEM images show nearly spherical particles with fairly distributed particles with an average crystallite size of about 14 nm. {sup 57}Fe Mössbauer spectral studies show well-resolved magnetic splitting in the Mn–Mg–Co oxide due to stronger superexchange interactions. FC and ZFC magnetization data revealed the superparamagnetic nature of the compounds investigated. Mn–Mg–Zn nanoparticles are blocked at about 206 K while the maximum blocking temperature of Mn–Mg–Co-nanosized oxide is above 300 K. These differences were discussed on the basis of Stoner-Wohlfath relation T{sub B} = KV /25k{sub B}.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2019

Efficiency enhancement in Si solar cell using 1D quasi-periodic antireflection coating

In order to enhance the efficiency of thin-film Si solar cell, two well-known Fibonacci and Thue–Morse sequences of 1D quasi-periodic structures have been considered to achieve a broadband (300–1100 nm) planar antireflection coating, in this article. As almost non-absorbing materials in the solar spectrum, TiO{sub 2} and SiO{sub 2} with optimized thicknesses are considered to eliminate the reflections in the front side of the solar cell. An optimized bilayer antireflection coating with thicknesses of 54.4 nm and 85.6 nm respectively for the TiO{sub 2} and SiO{sub 2} layers has been obtained. Considering material dispersion and solar power spectrum (AM1.5), maximum efficiency enhancements of 42.78%, 46.15%, and 50% have been achieved for the 3 µm thin-film Si solar cell using the FC(3,1) structure which correspond to the cells without any recombination, with bulk recombination, and with bulk and surface recombinations, respectively. The proposed quasi-periodic multilayer antireflection structures have been investigated and optimized using the TMM and FDTD methods. The electrical characteristic of the design is studied by the drift–diffusion method after extracting the electron–hole pair generation. Also, the stability of the performance of the proposed ARC against induced roughness in practice has been investigated and discussed.

14 SOLAR ENERGY↗
DOE OSTI2023

Structure of Rhizobium sp. 4-9 histamine dehydrogenase and analysis of the electron transfer pathway to an abiological electron acceptor

Histamine dehydrogenase from the gram-negative bacterium Rhizobium sp. 4-9 (HaDHR) is a member of a small family of dehydrogenases containing a covalently attached FMN, and the only member so far identified to date that does not exhibit substrate inhibition. Here, in this study, we present the 2.1 Å resolution crystal structure of HaDHR. This new structure allowed for the identification of the internal electron transfer pathway to abiological ferrocene-based mediators. Alanine 437 was identified as the exit point of electrons from the Fe 4 S 4 cluster. The enzyme was modified with a Ser436Cys mutation to facilitate covalent attachment of a ferrocene moiety. When modified with Fc-maleimide, this new construct demonstrated direct electron transfer from the enzyme to a gold electrode in a histamine concentration-dependent manner without the need for any additional electron mediators.

59 BASIC BIOLOGICAL SCIENCES↗