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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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At least 379 records · Page 21
All sourcesNASA NTRSDOE OSTI
DOE OSTI2015

Melter Feed Reactions at T ≤ 700°C for Nuclear Waste Vitrification

To understand feed‐to‐glass conversion for the vitrification of nuclear waste, we investigated batch reactions and phase transitions in a simulated nuclear waste glass melter feed heated at 5 K/min up to 700°C using optical microscopy, scanning electron microscopy with energy‐dispersive X‐ray spectroscopy, and X‐ray diffraction. To determine the content and composition of leachable phases, we performed leaching tests; the leachates were analyzed by inductively coupled plasma atomic emission spectroscopy. By 400°C, gibbsite and sodium borates lost water and converted to amorphous phase, whereas other metallic hydroxides dehydrated to oxides. Between 400°C and 700°C, carbonates decomposed before 500°C; amorphous aluminum oxide and calcium oxide reacted with the sodium borate and formed the more durable amorphous borate phase along with intermediate crystalline products; above 500°C, quartz began to dissolve, and hematite started to convert to trevorite.

Xu, Kai↗
DOE OSTI2012

Preliminary results of calculations for heavy-water nuclear-power-plant reactors employing {sup 235}U, {sup 233}U, and {sup 232}Th as a fuel and meeting requirements of a nonproliferation of nuclear weapons

A physical design is developed for a gas-cooled heavy-water nuclear reactor intended for a project of a nuclear power plant. As a fuel, the reactor would employ thorium with a small admixture of enriched uranium that contains not more than 20% of {sup 235}U. It operates in the open-cycle mode involving {sup 233}U production from thorium and its subsequent burnup. The reactor meets the conditions of a nonproliferation of nuclear weapons: the content of fissionable isotopes in uranium at all stages of the process, including the final one, is below the threshold for constructing an atomic bomb, the amount of product plutonium being extremely small.

21 SPECIFIC NUCLEAR REACTORS AND ASSOCIATED PLANTS↗
DOE OSTI2018

Asymptotic Normalization Coefficients (Nuclear Vertex Constants), Three-Body Asymptotic Normalization Functions (On-Shell Vertex Functions) and Nuclear Astrophysics

In the present review work, the main methods of the determination of asymptotic normalization coefficients (or respective nuclear vertex constants) for the A + x → B channel and of threebody asymptotic normalization functions (or respective on-shell vertex functions) for the A + b + c → B channel are briefly discussed. The main attention is paid both to the use of the specific asymptotic normalization coefficients and three-body asymptotic normalization functions as a source of getting the valuable information about the pair (nucleon–nucleon, nucleon–cluster and cluster–cluster) nuclear interactions and to their application for the specific direct nuclear-astrophysical radiative capture and peripheral transfer reactions at low energies.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2020

Gamma-ray spectrometry as a tool for exploring archaeological nuclear facilities: a case study from the Nevada Test Site Nuclear Rocket Development Station

Since its first demonstration in the early 2000s, the exploration of gamma-ray spectrometry (GRS) applications as a geophysical tool in archaeology remains nascent. While intentional neutron activation, which requires a gamma-ray analysis, has seen increasing use as a geoforensics technique in archaeology, little or no research has been published concerning the possibility of GRS as an industrial archaeological tool for use in exploring nuclear sites or facilities where neutron activation and surface contamination may have already occurred. Consequently, the use of GRS as a geophysical tool for the archaeological investigation of abandoned or decommissioned nuclear facilities is proposed, demonstrated, and discussed using a case study from the Nevada Test Site Nuclear Rocket Development Station.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2021

Chicago Pile-1 paved the way for nuclear science and a lab in Los Alamos First self-sustaining nuclear chain reaction was nearly 80 years ago

On a bitter-cold winter day, 43 scientists gathered at an abandoned squash court at the University of Chicago where they would ultimately enable a secret lab in Los Alamos to change the world just years later. It was December 2, 1942. The group, led by Italian physicist and Nobel laureate Enrico Fermi, stacked graphite bricks, piling 57 layers that totaled more than 770,000 pounds. Later named Chicago Pile-1, their goal was to create the world’s first self-sustaining, controlled nuclear chain reaction. Inside the approximately 20-feet-tall pile were smaller blocks of uranium and control rods that, when removed, would cause the reaction to go critical – meaning create a nuclear chain reaction. It was roughly $1 million worth of materials, equivalent to nearly $16 million today, and a concept that a nuclear chain reaction would allow the weaponization of the atom. “Its success would be the crucial proof needed to know it would be possible to create an atomic bomb,” said LANL Historian Roger Meade (C-NR). “This was the precursor to the Lab we have today, nearly 80 years later.”

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2019

Coating of nuclear fuel cladding materials, method for coating nuclear fuel cladding materials

The invention provides a nuclear reactor cladding, wherein at least one layer of coating is deposited on the exterior surface of the cladding. A nuclear reactor cladding, wherein at least one layer of coating is deposited on the interior surface of the cladding. A method of coating a nuclear reactor cladding, with the steps of selecting the cladding and depositing at least one layer of a first coating on the cladding.

22 GENERAL STUDIES OF NUCLEAR REACTORS↗
DOE OSTI2020

A highly-enriched 244 Pu reference material for nuclear safeguards and nuclear forensics measurements

A highly-enriched 244 Pu isotope dilution reference material has been prepared and characterized for metrologically traceable measurements of very small quantities of plutonium. The amount of plutonium in samples associated with nuclear safeguards and nuclear forensic measurements can be significantly less than 1 ng. Accordingly, the ability to quantify the amount and isotopic composition of plutonium from a single mass-spectrometric analysis is particularly desirable. The highly-enriched 244 Pu reference material, described here, will minimize the magnitude of spike corrections necessary to obtain accurate information on plutonium isotopic composition from isotope dilution measurements.

07 ISOTOPE AND RADIATION SOURCES↗
DOE OSTI2017

The Use of Positrons to Survey Alteration Layers on Synthetic Nuclear Waste Glasses

In order to safeguard society and the environment, understanding radioactive waste glass alteration mechanisms in interactions with solutions and near-field materials, such as Fe, is essential to nuclear waste repository performance assessments. Alteration products are formed at the surface of glasses after reaction with solution. In this study, glass altered in the presence of Fe0 in aqueous solution formed two alteration layers: one embedded with Fe closer to the surface and one without Fe found deeper in the sample. Both layers were found to be thinner than the alteration layer found in glass altered in aqueous solution only. For the first time, Doppler Broadening Positron Annihilation Spectroscopy (DB-PAS) is used to non-destructively characterize the pore structures of glass altered in the presence of Fe0. Advantages and disadvantages of DB-PAS compared to other techniques used to analyze pore structures for altered glass samples are discussed. Ultimately, DB-PAS has shown to be an excellent choice for pore structure characterization for glasses with multiple alteration layers. Monte Carlo modeling predicted positron trajectories through the layers, and helped explain DB-PAS data, which showed that the deeper alteration layer without Fe had a similar composition and pore structure to layers on glass altered in water only.

Doppler Broadening Positron Annihilation Spectrosc↗
DOE OSTI2011

Nuclear Data Sheets A=32

Nuclear spectroscopic information for experimentally investigated nuclides of mass 32 (Ne, Na, Mg, Al, Si, P, S, Cl, Ar) has been evaluated. The principal sources of the Adopted Levels presented for nuclides close to the stability line are Endt's evaluations (1990En08, 1978En02). The data sets for reactions and decays, including all available gamma-ray data, are based mostly on the original literature. Except for the half-life of {sup 32}Ne decay, no other details about its decay characteristics are available. Structure data for {sup 32}Ne and {sup 32}Na are limited to only one excited state in each. The {sup 32}Mg nuclide is of central and prime relevance in the 'island of inversion' at or near N = 20 semi-closed shell. The lifetime of only one excited state in {sup 32}Mg is known. The spin-parity assignments of several levels in this nucleus are not quite firm. The structure of {sup 32}Ar is limited to only one known state at low energy and two resonances in the giant-dipole excitation region. The {sup 32}P, {sup 32}S and {sup 32}Cl remain the most extensively studied nuclei through various reaction channels.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2015

Nuclear Data Sheets for A = 224

The experimental nuclear spectroscopic data for ten experimentally known nuclides of mass number 224 (Bi, Po, At, Rn, Fr, Ra, Ac, Th, Pa, U) have been evaluated and presented together with the Adopted properties for levels and γ rays. For {sup 224}Bi, {sup 224}Po, {sup 224}At, {sup 224}Rn, {sup 224}Fr, {sup 224}Pa and {sup 224}U nuclei, only the ground–state information is known. Half–lives of ground states of 224Bi and 224Po have not yet been measured. The decay of {sup 224}Rn to {sup 224}Fr has been studied, but no decay scheme has been proposed. The decay of {sup 224}Ac to {sup 224}Ra is reported only in an abstract style conference proceedings. For a definite Jπ assignment for ground state of {sup 224}Ac, a detailed study of this decay may be helpful. In the decay of {sup 228}Pa to {sup 224}Ac, authors of 1994Ah03 state that the lowest state observed in their work may not be the ground state. Thus an extensive study of {sup 228}Pa α decay, and studies involving nuclear reactions are warranted since the level scheme of {sup 224}Ac presented in this evaluation is considered as incomplete due to the lack of confirmed information about multipolarities, mixing ratios and other spectroscopic details. Three new nuclides {sup 224}Bi, {sup 224}Po, and {sup 224}At are added in this revision, together with new in–beam γ–ray and Coulomb excitation data for {sup 224}Ra. Although, not much new experimental data have appeared since the previous evaluation (1997Ar05), extensive modifications have been made in almost all the datasets. This work supersedes the information presented in the previous NDS evaluations of A = 224: 1997Ar05, 1986Ma45 and 1976El05.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2016

Nuclear Data Sheets for A = 41

Available information pertaining to the nuclear structure of all nuclei with mass numbers A=41 ranging from Al (Z=13) to Ti (Z=22) are presented. The experimental reaction and decay data are evaluated and any inconsistencies or discrepancies are noted. The adopted values for various level properties (such as the spin, parity and and halflife) and gamma properties (energy, intensity and multipole character) are given. Since the prior evaluation several new measurements have expanded our knowledge of A=41 nuclides. The half-life of the ground state of {sup 41}Si has been determined and a single excited state identified. Excited levels in {sup 41}P have been observed for the first time. In {sup 41}Cl, seven new excited states have been identified in deep inelastic and heavy ion transfer reactions. Half-lifes for four states in {sup 41}Ar have been updated and additional levels with gammas have been included from a new measurement using the multiple ion transfer reaction. In {sup 41}Ca via charge-exchange reaction measurements, several new excited states were observed. A number of new resonances in {sup 41}K have been identified via the (p,γ) reaction. There remains a significant discrepancy in the half-life of the first excited state (980 keV) in {sup 41}K, with measurements differing by more than an order of magnitude. Transfer reactions suggest that this M1 transition should be l-forbidden, however, several measurements yield a lifetime which suggests a sizable M1 strength. Further measurements to resolve the current conflicts would be beneficial.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2017

Nuclear Data Sheets for A=40

The experimental nuclear structure data and decay data are evaluated for the known nuclides of mass 40 (Mg, Al, Si, P, S, Cl, Ar, K, Ca, Sc, Ti). Detailed evaluated nuclear structure information is presented with the best values recommended for level energies, half-lives, γ-ray energies and intensities, decay properties (energies, intensities and placement of radiations), and other spectroscopic data. The {sup 40}Ca and {sup 40}K nuclides remain as the most extensively studied from many different reactions and decays; no excited states are known in {sup 40}Mg, {sup 40}Al, {sup 40}P and {sup 40}Ti. This work supersedes the earlier full evaluation of A=40 by J. Cameron and B. Singh (2004Ca38).

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2018

Nuclear Data Sheets for A=164

Experimental nuclear structure data for the known A=164 isobaric nuclides (Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Hf, Ta, W, Re, Os, Ir) have been evaluated, and presented together with Adopted properties of level energies, and associated γ rays. The decay data for these nuclides have also been evaluated, providing Adopted values of γ and β radiations, and log ft values. No excited states are known in 164 Eu, 164 Tb, and 164 Ir. Information for 164 Gd, 164 Re and 164 Os is limited due to insufficient experimental data. For radioactive nuclides, decay schemes of 164 Sm, 164 Gd and 164 Re are not known, and those of 164 W, 164 Tb, 164 Lu, 164 Hf, 164 Ta and 164 W are incomplete. The decay schemes of 164 Ho and the two activities of 164 Tm seem fairly complete. The decay scheme of 164 Yb presents a major problem that the Q(ε) value of 887 keV 29 recommended in 2017Wa10 is in disagreement with the population of levels at 928, 952 and 1060 keV in the daughter nucleus. This decay scheme, which so far has been mainly reported in a secondary reference (1982AdZZ) needs further investigation. Also the masses of 164 Yb and 164 Tm need either new measurements or a re-evaluation to resolve discrepancy of about 220 keV in the Q value of 164 Yb decay to 164 Tm. The reactions and decays for which no new experimental information has become available since the 2001 update have undergone revisions to incorporate conversion coefficients from BrIcc code, and evaluated Q values from 2017Wa10, but the essential content of such datasets may have remained the same as in previous evaluations. Finally, in this respect the present work greatly benefited from all the previous NDS evaluations (2001Si27,1992Sh07, 1986Sh03,1974Bu30), but at the same time data presented herein supersede all the previous published evaluations.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗
DOE OSTI2018

Nuclear Data Sheets for A=171

Experimental data pertaining to all nuclei with mass number A=171 (Tb, Dy, Ho, Er, Tm, Yb, Lu, Hf, Ta, W, Re, Os, Ir, Pt, Au, Hg) have been evaluated. Level schemes from both radioactive decay and reaction studies are presented, along with associated tables of experimental data and adopted properties for levels and γ rays. This evaluation for A=171, which considers data received by 30 June 2018, supersedes the 2002 evaluation (with a literature cutoff date of August 2002) by Coral M. Baglin, published in Nuclear Data Sheets 96, 399 (2002) and the subsequent evaluation of the ENSDF file for 171Pt by C. Baglin (literature cutoff date of 15 April 2010).

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2019

Nuclear Data Sheets for A=218

The evaluated data are presented for 11 known A=218 nulcides (Pb, Bi, Po, At, Rn, Fr, Ra, Ac, Th, Pa and U). For {sup 218}Pb, {sup 218}Bi, {sup 218}At and {sup 218}Pa, data are available only for the ground states. For {sup 218}U, only the g.s. and a high-spin isomer are known, with no data on γ-ray transitions available. For {sup 218}Po, ten excited states are known from {sup 218}Bi decay, with no knowledge on the multipolarities of gamma-ray transitions. For {sup 218}Th, five excited states in the g.s. band are known from an in-beam γ-ray study. Data on level half-lives, multipolarities and mixing ratios of gamma transitions is generally lacking for A=218 nuclei. The static magnetic dipole moment has been measured for only an isomer in {sup 218}Fr. With the exception of a new nuclide, {sup 218}Pb, and measurements of half-lives of ground states of a few nuclides of A=218 and A=222, no substantial structure information has become available since the previous evaluation in 2006. Q values are adopted from 2017Wa10 (AME-2016). The present evaluation supersedes the previous A=218 ENSDF evaluations, 2006Ja03, 1995El08, 1987El12 and 1977To13. This evaluation was carried out as part of a joint IAEA-ICTP workshop for Nuclear Structure and Decay Data, organized and hosted by the IAEA, Vienna, and ICTP, Trieste, October 15–26, 2018.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2014

Plutonium measurements with a fast-neutron multiplicity counter for nuclear safeguards applications

Measurements were performed at the Joint Research Centre in Ispra, Italy to field test a fast-neutron multiplicity counter developed at the University of Michigan. The measurements allowed the assessment of the system's photon discrimination abilities, efficiency when measuring neutron multiplicity, ability to characterize 240 Pu eff mass, and performance relative to a currently deployed neutron coincidence counter. We describe how this work is motivated by the need to replace and improve upon 3 He neutron detection systems for nuclear safeguards applications.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗