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At least 127 records · Page 7
All sourcesNASA NTRSDOE OSTI
DOE OSTI2022

Lifetime measurements of states of S 35 , S 36 , S 37 , and S 38 using the AGATA γ -ray tracking spectrometer

Lifetimes or lifetime limits of a small number of excited states of the sulfur isotopes with mass numbers A = 35 , 36, 37, and 38 have been measured using the differential recoil-distance method. The isotopes of sulfur were populated in binary grazing reactions initiated by a beam of 36 S ions of energy 225 MeV incident on a thin 208 Pb target which was mounted in the Cologne plunger apparatus. The combination of the PRISMA magnetic spectrometer and an early implementation of the AGATA γ-ray tracking array was used to detect γ rays in coincidence with projectile-like nuclear species. Lifetime measurements of populated states were measured within the range from about 1 to 100 ps. The number of states for which lifetime measurements or lifetime limits were possible was limited by statistics. For 35 S, the lifetime was determined for the first 1/2 + state at 1572 keV; the result is compared with a previous published lifetime value. The lifetime of the 3 - state of 36 S at 4193 keV was determined and compared with earlier measurements. No previous lifetime information exists for the (6 + ) state at 6690 keV; a lifetime measurement with large associated error was made in the present work. For 37 S, the states for which lifetime limits were established were those at 646 keV with J π = 3/2 - and at 2776 keV with J π = 11/2 - ; there are no previously published lifetime values for excited states of 37 S. Finally, a lifetime limit was established for the J π =(6 + ) state of 38 S at 3675 keV; no lifetime information exists for this state in the literature. Measured lifetime values were compared with the results of state-of-the-art shell-model calculations based on the PSDPF, SDPF-U, and FSU effective interactions. In addition, nuclear magnetic-dipole and electric-quadrupole moments, branching ratios, mixing ratios, and electromagnetic transition rates, where available, have been compared with shell-model values. The current work suffers from poor statistics; nevertheless, lifetime values and limits have been possible, allowing a useful discussion of the ability of state-of-the-art shell-model calculations to reproduce the experimental results.

electromagnetic transitions↗
DOE OSTI2014

β-decay spectroscopy of r-process nuclei with N = 126 at KISS

The β-decay properties of nuclei with N = 126, which are believed to act as progenitors in the rapid neutron capture (r-) process path forming the third peak (A ∼ 195) in the observed r-abundance element distribution, are considered critical for understanding the production of heavy elements such as gold and platinum at astrophysical sites. We have constructed the KEK Isotope Separation System (KISS), which consists of a gas cell based laser ion source (atomic number selection) and an isotope separation on-line (ISOL) (mass number selection), to produce pure low-energy beams of neutron-rich isotopes around N = 126 and to study their β-decay properties, which are also of interest for astrophysics. The isotopes of interest will be produced by multi-nucleon transfer reactions in heavy ion collisions (e.g. {sup 136}Xe projectile on {sup 198}Pt target). KISS will allow us to study unknown isotopes produced in weak reaction channels under low background conditions. We successfully extracted the stable {sup 56}Fe beam from KISS at the last commissioning on-line experiment with the extraction efficiency of 0.25% and beam purity of more than 98%. We can access the nuclei with N = 126 and measure their half-lives using the KISS in the case of the extraction efficiency of 0.1%.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2020

Evolution of collectivity in 118 Xe

A recoil-distance Doppler shift experiment has been performed using the Pd 102 ( F 19 , p 2 n ) reaction at a beam energy of 73 MeV to measure the lifetime of excited states in Xe 118 . Additionally, the differential decay-curve method using γ γ coincidences and a gating procedure that allows to extract the lifetime without feeding assumptions has been employed. The lifetimes obtained for the yrast states up to spin-parity 8 + are compared with interacting boson model calculations and Xe 118 can be classified as a transitional nucleus between the spherical and a deformed shape. Systematics of the B ( E 2 ) values for the 2 + → 0 + and 4 + → 2 + transitions in the isotopic chains of tin, tellurium and xenon are presented. It is proposed that a “critical point” exists at which the B ( E 2 ; 4 + → 2 + ) / B ( E 2 ; 2 + → 0 + ) ratio drops to unity for lower neutron numbers within the isotopic chain. The position of the “critical point” varies with proton number, i.e., it is presumed to be located at the same mass number A = 114 in the Sn, Te, and Xe isotopes.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
NASA NTRS1991

Aiming Schedule For Orbiting Astrometric Telescope

Report discusses schedule of observation times and aiming directions of proposed astrometric telescope facility mounted on Space Station in orbit around Earth. Primarily makes repeated observations of apparent positions of each of 127 selected stars with respect to distant reference stars in same field of view known to have unperturbed proper motions. Purpose of observations to detect motions of selected stars about centers of mass and to analyze harmonic content of motions to infer existence, number, masses, and orbital radii of planets.

Mascy, Alfred C.↗
DOE OSTI2018

Mass measurements of neutron-rich indium isotopes toward the N = 82 shell closure

Precise mass measurements of the neutron-rich 125–130 In isotopes have been performed with the TITAN Penning trap mass spectrometer. TITAN's electron beam ion trap was used to charge breed the ions to charge state q = 13+ thus providing the necessary resolving power to measure not only the ground states but also isomeric states at each mass number. Here, the properties of the ground states are investigated through a series of mass differentials, highlighting trends in the indium isotopic chain as compared to its proton-magic neighbor, tin (Z = 50). In addition, the energies of the indium isomers are presented. The (8 - ) level in 128 In is found to be 78 keV lower than previously thought and the (21/2 - ) isomer in 127 In is shown to be lower than the literature value by more than 150 keV.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
NASA NTRS1971

Diffusing capacity and anatomic dead space for carbon-18 monoxide.

Carbon monoxide (CO) is difficult to measure with a respiratory mass spectrometer because of the similar mass numbers of CO and nitrogen, but this is possible using carbon-18 monoxide. The mass resolution, signal-to-noise ratio, linearity, and background were all found to be adequate. The measurement of the single-breath diffusing capacity was examined. Unless the mean alveolar volume during breath holding is used in the calculation, the value for Dco obtained depends on which portion of the alveolar sample is analyzed. The anatomic dead space for CO was found to be almost the same as that for argon suggesting that the diffusion rate at the dead space-alveolar gas interface was not greatly affected by the alveolar concentration of the gas.

Wagner, P. D.↗
DOE OSTI2018

Pion-less effective field theory for atomic nuclei and lattice nuclei

Here, we compute the medium-mass nuclei 16 O and 40 Ca using pionless effective field theory (EFT) at next-to-leading order (NLO). The low-energy coefficients of the EFT Hamiltonian are adjusted to experimantal data for nuclei with mass numbers A = 2 and 3, or alternatively to results from lattice quantum chromodynamics (QCD) at an unphysical pion mass of 806 MeV. The EFT is implemented through a discrete variable representation in the harmonic oscillator basis. This approach ensures rapid convergence with respect to the size of the model space and facilitates the computation of medium-mass nuclei. At NLO the nuclei 16 O and 40 Ca are bound with respect to decay into alpha particles. Binding energies per nucleon are 9-10 MeV and 30-40 MeV at pion masses of 140 MeV and 806 MeV, respectively.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2019

Nuclear Data Sheets for A=266,270,274,278,282,286,290,294,298☆

Spectroscopic information such as production, identification, half-lives, decay modes and possible excited states for experimentally known nuclides of mass numbers 266, 270, 274, 278, 282, 286, 290, 294, and 298 are presented together with the recommended values, superseding information and data in the previous ENSDF and NDS evaluation by 2005Gu33. No nuclides have yet been identified for A=302. In the last 14 years, large amounts of new and definitive data on the superheavy nuclides (SHN) have become available, thus changing almost entirely the landscape of nuclear data in this mass region, as also indicated by a number of recent review articles: 2017Og01, 2016Ho09, 2016Ho06 (for fission barriers), 2015Og05, 2015Og07, 2015Mo25, 2015OgZX, 2013Th02, and 2011Og07. See 2016Ka49 for IUPAC technical discussions for the discovery of Z=117 (Ts), Z=115 (Mc), Z=113 (Nh), 2001Ka70 and 2003Ka71 for Z=110-112, 2011Ba54 for Z≥113, 2009Ba62 for Z=112, and 2016Ka50 for Z=118 (Og). A special issue of Nuclear Physics A444 (2015) is devoted to research on superheavy elements (SHE) with 27 articles. In particular, see article by 2015Ko20 on mass spectrometric searches for superheavy elements in terrestrial matter. See also Proceedings of Nobel Symposium NS160 ‘Chemistry and Physics of Heavy and Superheavy Elements’ published in Eur. Phys. Jour. Web of Conferences 131 (2016), in particular 2016UtZZ, 2016DmZZ and 2016HoZY. See also 2016DuZX for future prospects of discovery of elements beyond Z=118 A=266: {sup 266}Db, {sup 266}Sg, {sup 266}Bh, {sup 266}Hs and {sup 266}Mt are the experimentally identified nuclides with A=266. Identification of {sup 266}Lr from α decay of {sup 270}Db has been proposed by 2014Kh04 from experiments at GSI, but complete details and analyses of all the four decay chains reported in this experiment have not yet been published, and discussion in 2015Og05 review article considering their work from Dubna (2013Og04, 2011Og04) and from GSI (2014Kh04) still concluded that {sup 270}Db decayed dominantly by SF mode, in contrast with dominant α decay mode proposed by 2014Kh04. Experiments carried out at FLNR-JINR-Dubna in collaboration with LLNL and ORNL, GSI-SHIP facility, RIKEN, and LBNL facilities: {sup 266}Db from the α-decay of {sup 282}Nh in two correlated decay chains at Dubna; {sup 266}Sg as α-daughter of {sup 270}Hs in 12 correlated decay chains at Dubna and GSI; {sup 266}Bh in α decay of {sup 278}Nh in three correlated decay chains observed at RIKEN, and also directly with one event in {sup 249}Bk({sup 22}Ne,5n) at LBNL, and with four events in {sup 243}Am({sup 26}Mg,3n) at HIRFL-Lanzhou; {sup 266}Hs as α-daughter of {sup 270}Ds at GSI in two different experiments, six correlated decays in the first, and 25 decay chains in the second experiment, the analysis of which has not been fully reported as yet; and {sup 266}Mt directly in {sup 209}Bi({sup 58}Fe,n) reaction at GSI in two different experiments, observing three events in the first experiment and 12 events in the second, also produced in {sup 208}Pb({sup 59}Co,n) reaction at LBNL, observing five correlated decay chains. See also 2000Ho27 for discussion on {sup 266}Sg and {sup 266}Mt. A=270: {sup 270}Db, {sup 270}Bh, {sup 270}Hs, {sup 270}Mt and {sup 270}Ds are the experimentally identified nuclides with A=270 are presented. Experiments carried out at FLNR-JINR-Dubna in collaboration with LLNL and ORNL, GSI-SHIP facility, and RIKEN: {sup 270}Db from the decay of {sup 294}Ts in six correlated decay chains at Dubna and GSI; {sup 270}Bh as α great-granddaughter of {sup 282}Nh in two correlated decay chains observed at Dubna; {sup 270}Hs directly in {sup 248}Cm({sup 26}Mg,4n) reaction at GSI, and in {sup 226}Ra({sup 48}Ca,4n) reaction at Dubna; {sup 270}Mt as granddaughter of {sup 278}Ts in three correlated decay chains at RIKEN; and {sup 270}Ds directly in {sup 207}Pb({sup 64}Ni,n) at GSI in 33 correlated decay chains. A=274: {sup 274}Bh, {sup 274}Mt and {sup 274}Rg are the experimentally identified nuclides with A=274. Search for {sup 274}Ds in {sup 238}U({sup 40}Ar, 4n),E=5.7 MeV/nucleon reaction and subsequent α decays at GSI (1990Sc11) proved negative. Experiments carried out at FLNR-JINR-Dubna in collaboration with LLNL and ORNL, GSI-SHIP facility, and RIKEN: {sup 274}Bh from the decay of {sup 294}Ts in six correlated decay chains at Dubna and GSI, {sup 274}Mt produced as α daughter of {sup 282}Nh in two correlated decay chains observed at Dubna, and {sup 274}Rg as α daughter of {sup 278}Nh produced in three correlated decay chains at RIKEN. A=278: {sup 278}Mt, {sup 278}Rg and {sup 278}Nh are the experimentally identified nuclides with A=278. A very tentative evidence is provided for {sup 278}Bh and {sup 278}Hs from a chain originally observed and assigned to {sup 289}Fl by 1999Og10, but later reassigned by 2004Og10 to {sup 290}Fl, and further discussed in detail by 2016Ho09, where, based on systematics of α decays and SF half-lives, {sup 290}Fl is proposed to decay via ε mode to {sup 290}Nh, which then decays by an α chain, ending in {sup 278}Bh that decays by SF mode. Experiments carried out at FLNR-JINR-Dubna in collaboration with LLNL and ORNL labs in the USA, GSI-SHIP facility, and RIKEN: {sup 278}Mt from the decay of {sup 294}Ts in six correlated decay chains at Dubna and GSI, {sup 278}Rg produced as α daughter of {sup 282}Nh in two correlated decay chains observed at Dubna, and {sup 278}Nh produced directly in three correlated decay chains at RIKEN. A=282: {sup 282}Rg, {sup 282}Cn and {sup 282}Nh are the experimentally identified nuclides with A=282. A very tentative evidence is provided for {sup 282}Mt and {sup 282}Ds from a chain originally observed and assigned to {sup 289}Fl by 1999Og10, but later reassigned by 2004Og10 to {sup 290}Fl, and further discussed in detail by 2016Ho09, where, based on systematics of α decays and SF half-lives, {sup 290}Fl is proposed to decay via ε mode to {sup 290}Nh, which then decays by an α chain, ending in {sup 278}Bh that decays by SF mode. Experiments carried out at FLNR-Dubna, in collaboration with LLNL and ORNL labs in the USA, and at GSI-SHIP facility confirm the identification of these isotopes, {sup 282}Rg in α decay chain of {sup 294}Ts in six correlated decay chains at Dubna and GSI, {sup 282}Cn produced in four ways at Dubna: independently in one correlated decay chain, as α daughter of {sup 286}Lv in 11 correlated decay chains, as α grand-daughter of {sup 290}Lv in 12 correlated decay chains, as α great-grand daughter of {sup 294}Og in four correlated decay chains, and {sup 282}Nh produced at Dubna directly in two correlated decay chains. A=286: {sup 286}Nh and {sup 286}Fl are the only experimentally identified nuclides with A=286. A very tentative evidence is provided for {sup 286}Rg and {sup 286}Cn from a chain originally observed and assigned to {sup 289}Fl by 1999Og10, but later reassigned by 2004Og10 to {sup 290}Fl, and further discussed in detail by 2016Ho09, where, based on systematics of α decays and SF half-lives, {sup 290}Fl is proposed to decay via ε mode to {sup 290}Nh, which then decays by an α chain, ending in {sup 278}Bh that decays by SF mode. 2017Ka66 in experiments at RIKEN using GARIS separator interpret one correlated decay chain in three different ways, one involving possible production of {sup 294}Lv in {sup 248}Cm({sup 48}Ca,2n),E=261.6 MeV, and α decay to {sup 290}Fl which further decays to {sup 286}Cn. Experiments carried out at FLNR-Dubna, in collaboration with LLNL and ORNL labs in the USA, and at GSI-SHIP facility confirm the identification of these isotopes, {sup 286}Nh as α grand-daughter of {sup 294}Ts in six correlated decay chains, and {sup 286}Fl produced in three ways: independently in 11 correlated decay chains, as α daughter of {sup 290}Lv in 12 correlated decay chains, and as α grand-daughter of {sup 294}Og in four correlated decay chains. A=290: {sup 290}Mc and {sup 290}Lv are the only experimentally identified nuclides with A=290. A tentative evidence is provided for {sup 290}Nh and {sup 290}Fl from a chain originally observed and assigned to {sup 289}Fl by 1999Og10, but later reassigned by 2004Og10 to {sup 290}Fl, and further discussed in detail by 2016Ho09, where, based on systematics of α decays and SF half-lives, {sup 290}Fl is proposed to decay via ε mode to {sup 290}Nh, which then decays by an α chain, ending in {sup 278}Bh that decays by SF mode. 2017Ka66 in experiments at RIKEN using GARIS separator interpret one correlated decay chain in three different ways, one involving possible production of {sup 294}Lv in {sup 248}Cm({sup 48}Ca,2n),E=261.6 MeV, and α decay to {sup 290}Fl. Experiments carried out at FLNR-Dubna, in collaboration with LLNL and ORNL labs in the USA, and at GSI-SHIP facility confirm the identification of these isotopes, {sup 290}Mc as α daughter of {sup 294}Ts in six correlated decay chains, and {sup 290}Lv produced in two ways, independently in 14 correlated decay chains, and as α daughter of {sup 294}Og in four correlated decay chains. A=294: {sup 294}Ts and {sup 294}Og are the only experimentally identified nuclides with A=294. Experiments carried out at FLNR-Dubna, in collaboration with LLNL and ORNL labs in the USA, and at GSI-SHIP facility confirm the identification of these isotopes, with a total of six EVR-α-SF correlated decay chains observed for {sup 294}Ts and four for {sup 294}Og. Tentative identification of {sup 294}Lv is provided by 2017Ka66 from the observation one correlated event using GARIS-RIKEN facility, where this event is interpreted in three possible ways, two interpretations lead to production of {sup 293}Lv and successive odd-A nuclides of {sup 289}Fl, {sup 285}Cn and {sup 281}Ds, whereas the third prediction starts with the production of {sup 294}Lv and successive {sup 290}Fl and {sup 286}Cn nuclides. Search for {sup 294}Rg in natural gold materials (2011De03), and for {sup 294}Ds, {sup 294}Fl and {sup 294}Mc in natural Pt, Pb and Bi samples (2011De21) using accelerator mass spectroscopy (AMS) proved negative, with extremely low upper limits established. Also 1980St05 did not see any evidence for {sup 294}Ds in natural Pt sample using AMS. A=298: Search for {sup 298}120 through fusion-evaporation reaction at Dubna, and for {sup 298}Fl and {sup 298}Mc in natural Pt, Pb and Bi samples using accelerator mass spectroscopy (AMS) proved negative. Tentative assignment of three α-α-α decay chains by 2016Ho09 to {sup 299}120 in {sup 248}Cm({sup 54}Cr,3n){sup 299}120 at GSI was refuted by 2017He11, assigning these correlations to random events, instead. A=302: Fluorescent x rays from Z=120 element were observed by 2012Fr03 from compound nucleus {sup 302}120 produced in {sup 238}U({sup 64}Ni,X),E=6.6 MeV/nucleon at GANIL, and x-ray yields were measured, together with minimum average time deduced from x-ray multiplicity. The compound nucleus could decay by 3n- or 4n-channels to produce {sup 299}120 or {sup 298}120. 2012He05 and 2016Ho09 also produced {sup 302}120 compound nucleus in {sup 248}Cm({sup 54}Cr, xn){sup 302}120{sup *},E=6.035 MeV/nucleon; and {sup 238}U({sup 64}Ni,xn){sup 302}120{sup *},E=5.53 MeV/nucleon reactions using UNILAC at GSI. Three α-α-α correlated decays from {sup 248}Cm({sup 54}Cr,xn){sup 302}120{sup *} reaction were tentatively assigned by 2016Ho09 to {sup 299}120 decay, however, a detailed analysis by 2017He11 refuted this claim, ascribing these events to random sequences. There are no data tables for A=302.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2020

Timescales of Quantum Equilibration, Dissipation and Fluctuation in Nuclear Collisions

Understanding the dynamics of equilibration processes in quantum systems as well as their interplay with dissipation and fluctuation is a major challenge in quantum many-body theory. The timescales of such processes are investigated in collisions of atomic nuclei using fully microscopic approaches. Findings from time-dependent Hartree-Fock and time-dependent random-phase approximation calculations are compared for 13 systems over a broad range of energies. The timescale for full mass equilibration ( ~ 2 × 10 - 20 s ) is found to be much larger than timescales for neutron-to-proton equilibration, kinetic energy, and angular momentum dissipations which are on the order of 10 - 21 s . Fluctuations of mass numbers in the fragments and correlations between their neutron and proton numbers build up within only a few 10 - 21 s . This suggests that dissipation is basically not impacted by mass equilibration, but is mostly driven by the exchange of nucleons between the fragments.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2020

Measurement and microscopic description of odd–even staggering of charge radii of exotic copper isotopes

Nuclear charge radii globally scale with atomic mass number A as A 1/3 , and isotopes with an odd number of neutrons are usually slightly smaller in size than their even-neutron neighbours. This odd–even staggering, ubiquitous throughout the nuclear landscape1, varies with the number of protons and neutrons, and poses a substantial challenge for nuclear theory. Here, we report measurements of the charge radii of short-lived copper isotopes up to the very exotic 78 Cu (with proton number Z = 29 and neutron number N = 49), produced at only 20 ions s –1 , using the collinear resonance ionization spectroscopy method at the Isotope Mass Separator On-Line Device facility (ISOLDE) at CERN. We observe an unexpected reduction in the odd–even staggering for isotopes approaching the N = 50 shell gap. To describe the data, we applied models based on nuclear density functional theory and A-body valence-space in-medium similarity renormalization group theory. Through these comparisons, we demonstrate a relation between the global behaviour of charge radii and the saturation density of nuclear matter, and show that the local charge radii variations, which reflect the many-body polarization effects, naturally emerge from A-body calculations fitted to properties of A ≤ 4 nuclei.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2025

Competition between mass-symmetric and asymmetric fission modes in 258 Md produced in the 4 He+ 254 Es reaction

Earlier studies of spontaneous fission of heavy actinides found that the fission-fragment mass distribution suddenly changes from predominantly asymmetric to symmetric, when the mass number of the fissioning nucleus becomes larger than A c = 257. We have measured for the first time fission-fragment mass and totalkinetic-energy (TKE) distributions of the excited compound nucleus 258 Md∗ (Z = 101), populated in the reaction 4 He + 254 Es, using the rare radioactive target isotope 254 Es with a short half-life, T1/2 = 275.7 d. The fission of 258 Md∗ can be interpreted as involving three fission modes: one mass-asymmetric and two mass-symmetric fission modes, the latter two are manifested by different TKE values. In this assumption, symmetric and asymmetric fission modes have nearly similar yields at the excitation energy of 15.0 MeV. The spectrum of 18.0 MeV can be explained as due to the increase of asymmetric fission mode.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
NASA NTRS1972

Comparative performance of double-focus and quadrupole mass spectrometers

Light-weight flight type double focus and quadruple mass spectrometer models were compared. Data cover size, weight, and power sensitivity required to achieve same resolution sensitivity at given mass number. Comparison was made using mathematical relationships. Analysis was confined to equal ion source area sensitivity variations not more than 40% over mass range.

Wilson, S. K.↗
DOE OSTI2019

Mass Spectrometry of a Xylitol Molecule

The technique and results of a mass spectrometric study on the yield of positive ions formed upon ionization of xylitol molecules by electron impact are discussed. The mass spectra of xylitol are studied in the range of mass numbers of 10–160 Da and in the range of bombarding electrons energies of 5–80 eV. Based on the analysis of the measured mass spectra, a scheme of xylitol fragmentation is proposed, which contains the most probable channels of formation of ion-fragments upon electron impact, when the energy of the incident electrons significantly exceeds the ionization potential of the molecule. The appearance energies of ionized fragments of xylitol are determined for the first time from the energy dependences of the effective cross-section formation of the ions upon electron impact. The dynamics of ionized fragment formation is studied in the temperature range of the initial substance evaporation of 340–410 K. The behavior of the temperature dependence indicates that the formation processes of water and oxonium cations compete with each other.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2022

The Status and Ambitions of the US Heavy Element Program

The aim of this whitepaper is to highlight the current capabilities and priorities of the US Heavy Element community and to provide the framework for a coordinated advancement of nuclear science from these studies. This is an organized effort to reflect on what has been achieved in the field given the recommendations and initiatives of the 2015 NSAC Long Range Plan, and on what can be realized in the next decade given current and possibly expanded investments. Current investments have positioned the US community to be among the world leaders in studies of the nuclear and chemical properties of the heaviest elements. These include studies of reaction mechanisms, moving us ever closer to the “island of stability”, in spectroscopy, allowing us to better understand nuclear structure at these extreme proton numbers, in chemical behavior, looking to determine how these elements should be placed on the Periodic Table, in performing the first measurements where isotopes are directly identified by their mass numbers, and in laying the foundation for a potential US-led new element discovery experiment. At present, the highest priority of the US Heavy Element community is to capitalize on the current investments by supporting the operations of US facilities at optimal values. These facilities include the Argonne Tandem Linac Accelerator System at Argonne National Laboratory and other Department of Energy facilities such as the 88-Inch Cyclotron at Lawrence Berkeley National Laboratory, which has a dedicated superheavy element program, as well as university laboratories, including Texas A&M University. The High Flux Isotope Reactor at Oak Ridge National Laboratory is crucial to providing the radioactive isotopes required for heavy element science targets. This facility should be supported to provide the actinide materials that are essential for US-based science. Production of stable, rare isotopes for beam material, including 48 Ca, 50 Ti, 54 Cr and 58 Fe, at the Stable Isotope Production and Research Center is critical to continued research in heavy element science and should be a priority. The continued development of targets for heavy element science and retaining US-based expertise is critical for the heavy element community. This is an area that is currently under pressure. For example, the target laboratory at Argonne National Laboratory serves a broad community and is currently under threat due to loss of critical personnel. The skills needed to make targets for nuclear science and develop new targetry methods need to be supported long term at Argonne, Oak Ridge and Lawrence Livermore National Laboratories as well as maintaining the programs at Oregon State University and San José State University as vital pipelines for training students. Advances in theory are the foundation to understand how nuclei behave and to predict those behaviors in new circumstances. Progress in these studies will necessitate continued and new investment and access to high-performance computing. The future health of the heavy element field is dependent on the continuous support of talented early-career professionals at all levels. It is critical that opportunities continue to be created for the next generation to become established in heavy element research so that we can ensure the field is attracting and retaining the best minds for continued success. It is also clear that to ensure diversity of ideas, perspectives and techniques, we need to recruit diverse personnel that are trained at the best facilities. The heavy element community is in support of continued investment to programs with initiatives in diversity, equity, and inclusion. Looking to the next decade of research, support needs to maintain and grow US leadership in heavy element science. Specifically, new investments in state-of-the-art instrumentation will be essential to scientific development of the field and in expanding scientific knowledge. Advances in the next generation of electron cyclotron resonance ion sources, multi-reflection time-of-flight devices, laser spectroscopy, trapping methods and next generation alpha and gamma spectroscopy systems should be prioritized.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗
DOE OSTI2015

Configuration splitting and gamma-decay transition rates in the two-group shell model

Expressions for reduced gamma-decay transition rates were obtained on the basis of the twogroup configuration model for the case of transitions between particles belonging to identical groups of nucleons. In practical applications, the present treatment is the most appropriate for describing decays for odd–odd nuclei in the vicinity of magic nuclei or for nuclei where the corresponding subshells stand out in energy. Also, a simple approximation is applicable to describing configuration splitting in those cases. The present calculations were performed for nuclei whose mass numbers are close to A ∼ 90, including N = 51 odd—odd isotones.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2026

SAM Code Enhancements for Fission Product Tracking of Noble Gases and Metals in MSRs

This report documents fiscal year 2026 enhancements to the System Analysis Module (SAM) for modeling fission product transport in liquid-fueled molten salt reactors (MSRs). The work advances three principal areas: noble gas transport, noble metal deposition, and user interface improvements. The noble gas transport capability integrates drift-flux gas transport, Henry’s law two-film interphase mass transfer with pressure-based nucleation suppression, Knudsen-regime pore diffusion into porous graphite with a conjugate salt-graphite interface constraint, built-in material properties, five Sherwood-number mass transfer correlations including three derived from high-fidelity NekRS simulations, and xenon-135 reactivity feedback through SAM’s point-kinetics model. This work also presents a comprehensive verification test suite, including new analytically verified cases for pressure-dependent onset of interphase gas transfer in a stagnant vertical pipe, a postulated FLiBe-graphite Xe extraction permeator, a gravity riser with a fission-product source, and a descending pipe with gas redissolution driven by hydrostatic pressure. A machine learning framework for bubble rise velocity prediction in molten salt systems is developed and benchmarked on molten-salt and diverse aqueous bubble datasets. The best-performing fine-tuned transfer-learning networks achieve an 82% reduction in RMSE relative to the Clift correlation, and is implemented directly in SAM. The noble metal transport capability is developed, including a liquid-wall deposition model and a gas-surface flotation mechanism that transfers insoluble particles entrained by sparging gas to wetted structures. Verification tests and demonstration cases cover the surface deposition, flotation efflux, and flotation shedding. Finally, a new [SpeciesTransport] input structure replaces positional global vectors with selfcontained, order-independent, named species blocks, simplifies the specification of multiphase species and decay chains, and remains fully compatible with existing SAM input files. Together, these developments improve the physical fidelity, verification basis, and usability of SAM for system-level analyses of fissionproduct behavior in MSRs.

Mui, Travis (ORCID:0000000303736470)↗
DOE OSTI2023

Description of the multinucleon transfer mechanism for Ca 48 + Pu 244 and Kr 86 + Pt 198 reactions in a quantal transport approach

Multinucleon transfer (MNT) reactions involving heavy projectile and target combinations stand as a promising method for synthesizing new neutron-rich exotic nuclei, which may not be possible using hot or cold fusion reactions or fragmentation. Exploring the mechanisms behind MNT reactions is essential and it requires a comprehensive theoretical framework that can explain the physical observables in these reactions. This work aims to show that the quantal diffusion approach based on the stochastic mean-field (SMF) theory is capable of explaining the reaction dynamics observed in MNT reactions. Primary product mass distributions in 48 Ca + 244 Pu reaction at E c.m. = 203.2 MeV and 86 Kr + 198 Pt reaction at E c.m. = 324.2 MeV are calculated and compared with the available experimental data. In this work, we utilize the time-dependent Hartree-Fock (TDHF) calculations to analyze the mean-field reaction dynamics computationally in the reactions 48 Ca + 244 Pu and 86 Kr + 198 Pt for a broad range of initial angular momenta. Quantal transport description based on the SMF approach is used to calculate quantal diffusion coefficients and mass variances in 48 Ca + 244 Pu and 86 Kr + 198 Pt systems. The primary products arising from quasifission reactions are described by joint probability distribution in the SMF approach and those arising from fusion-fission are estimated by using the statistical deexcitation code gemini + +. Mean values of charge and mass numbers, scattering angles of the primary reaction products, and the total kinetic energies after the collision are calculated within the TDHF framework for a broad range of initial angular momenta. Throughout all the collisions, drift toward the mass symmetry and large mass dispersion associated with this drift are observed. Here, the calculated primary fragment and mass distributions using the SMF approach successfully explain experimental observations for the 48 Ca + 244 Pu and 86 Kr + 198 Pt systems. The primary mass distributions, mean values of binary products, and mass dispersions are determined and results are compared with the available experimental data. The observed agreement between the experimental data and SMF results highlights the effectiveness of the quantal diffusion mechanism based on the SMF approach, which does not include any adjustable parameters other than standard parameters of Skyrme energy density functional.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2018

Simulation of density fluctuations before the L-H transition for Hydrogen and Deuterium plasmas in the DIII-D tokamak using the BOUT++ code

A six-field two-fluid model has been used to simulate density fluctuations. The equilibrium is generated by experimental measurements for both Deuterium (D) and Hydrogen (H) plasmas at the lowest densities of DIII-D low to high confinement (L-H) transition experiments. In linear simulations, the unstable modes are found to be resistive ballooning modes with the most unstable mode number n=30 or $k_\theta\rho_i\sim0.12$ . The ion diamagnetic drift and $E\times B$ convection flow are balanced when the radial electric field (E r ) is calculated from the pressure profile without net flow. The curvature drift plays an important role in this stage. Two poloidally counter propagating modes are found in the nonlinear simulation of the D plasma at electron density $n_e\sim1.5\times10^{19}$ m -3 near the separatrix while a single ion mode is found in the H plasma at the similar lower density, which are consistent with the experimental results measured by the beam emission spectroscopy (BES) diagnostic on the DIII-D tokamak. The frequency of the electron modes and the ion modes are about 40kHz and 10 kHz respectively. The poloidal wave number $k_\theta$ is about 0.2 cm -1 ($k_\theta\rho_i\sim0.05$ ) for both ion and electron modes. The particle flux, ion and electron heat fluxes are~3.5–6 times larger for the H plasma than the D plasma, which makes it harder to achieve H-mode for the same heating power. The change of the atomic mass number A from 2 to 1 using D plasma equilibrium make little difference on the flux. Increase the electric field will suppress the density fluctuation. In conclusion, the electric field scan and ion mass scan results show that the dual-mode results primarily from differences in the profiles rather than the ion mass.

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗