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At least 19 records

Impact of triaxiality on the rotational structure of neutron-rich rhenium isotopes

A number of 3-quasiparticle isomers have been found and characterised in the odd-mass, neutron-rich, Re-187, Re-189 and Re-191 nuclei, the latter being four neutrons beyond stability. The decay of the isomers populates states in the rotational bands built upon the 9/2(-)[514] Nilsson orbital. These bands exhibit a degree of signature splitting that increases with neutron number. This splitting taken together with measurements of the M1/E2 mixing ratios and with the changes observed in the energy of the gamma-vibrational band coupled to the 9/2(-)[514] state, suggests an increase in triaxiality, with gamma values of 5 degrees, 18 degrees and 25 degrees deduced in the framework of a particle-rotor model. (C) 2015 Published by Elsevier B.V.

neutron-rich↗

Rhenium Isotope Reconnaissance of Uranium Ore Concentrates

Exploration of natural isotopic variations of the element rhenium (Re) is in its infancy, with initial studies revealing isotopic fractionation in a variety of geological materials. Here, in this work, we investigate Re isotope variation as a new geochemical tool, given its redox-sensitive properties and affinity for organic matter and sulfides. In this work, Re abundance and isotope ratio data were collected from uranium ore concentrates (UOCs) across a variety of depositional ages, locations, geologic settings, and deposit types. Ore types from which the UOC were derived include sandstone, unconformity, and quartz-pebble (QP) conglomerate. To isolate Re from the U-rich matrix of UOCs, a new purification method utilizing DGA ion exchange resin was developed. We found that UOCs exhibit a wide range of Re isotope ratios, with sandstone ore-derived UOCs having the isotopically lightest values, QP conglomerate ore-derived UOCs having the heaviest, and unconformity ore-derived UOCs in between (with some overlap with sandstone UOCs). The Re isotope ratio range observed in UOCs extends previously reported values by more than a factor of two. Industrial processing (e.g., incomplete recovery of Re from ore, contamination, fractionation during processing) may play a role in the isotopic variability in the UOCs. However, systematic differences between ore types suggest that the depositional setting is a significant factor. For nuclear forensic investigations, Re isotopic compositions combined with data from other isotopic systems provide geochemical signatures that can aid in provenance assessment of UOCs. Regardless of the specific causes for the wide range of Re isotope ratios in UOCs, these initial data indicate Re is a promising tool for nuclear forensic investigations on samples from early in the nuclear fuel cycle.

58 GEOSCIENCES↗

Rhenium-osmium-isotope constraints on the age of iron meteorites

Rhenium and osmium concentrations and the osmium isotopic compositions of iron meteorites were determined by negative thermal ionization mass spectrometry. Data for the IIA iron meteorites define an isochron with an uncertainty of approximately +/-31 million years for meteorites about 4500 million years old. Although an absolute rhenium-osmium closure age for this iron group cannot be as precisely constrained because of uncertainty in the decay constant of Re-187, an age of 4460 million years ago is the minimum permitted by combined uncertainties. These age constraints imply that the parent body of the IIAB magmatic irons melted and subsequently cooled within 100 million years after the formation of the oldest portions of chondrites. Other iron meteorites plot above the IIA isochron, indicating that the planetary bodies represented by these iron groups may have cooled significantly later than the parent body of the IIA irons.

Horan, M. F.↗

Rhenium-osmium isotope systematics in meteorites. I - Magmatic iron meteorite groups IIAB and IIIAB

Resonance ionization mass spectrometry is used to determine the Re and Os abundances by isotope dilution (ID) and to measure Os-187/Os-186 ratios from 19 iron meteorites. Abundances range from 1.4 to 4800 ppb Re, and from 13 to 65,000 ppb Os, and generally agree well with previous ID and neutron activation results. The Re and Os data suggest that abundance trends in these iron groups may be entirely explained by fractional crystallization. Whole-rock isochrons for the IIAB and IIIAB groups are statistically indistinguishable. Pooled data yield an initial Os-187/Os-186 of 0.794 +/- 0.010 Ga. Given the errors in the slope and half life, this age does not differ significantly from the canonical chondrite age of 4.56 Ga, but could be as young as 4.46 Ga.

Morgan, John W.↗

Rhenium-osmium isotope systematics of Group 2A and Group 4A iron meteorites

We are investigating the Re-Os isotope systematics of two groups of magmatic iron meteorites (2A, 4A) in an attempt to establish precise 'total rock' isochrons by the Re-Os system. The Re-187/Os-187 isotope system is recognized as a method by which the ages of iron meteorites can be directly determined and that can provide information on the timing of FeNi segregation and core formation in planetesimals. The Re-Os isotope system permits the direct absolute dating of the metal phase in iron meteorites. Indirect dating of iron meteorites has been achieved in the past through the Rb-Sr, K-Ar, and most recently, Sm-Nd for silicate inclusions, where present. Relative dating has been obtained directly by extensive studies of the short-lived system Pd-107/Ag-107 for the metal and sulfide phases and indirectly using I-129/Xe-129 in silicate and sulfide inclusions.

Creaser, R. A.↗

Rhenium-osmium isotope systematics of ordinary chondrites and iron meteorites

Using negative thermal ionization mass spectrometry, Re and Os abundances were determined by isotope dilution and Os-187/Os-186 measured in 11 ordinary chondrites, and also in 1 IIB and 3 IIIB irons. In addition, Os-186/Os-188 and Os-189/Os-188 ratios were precisely determined for 3 unspiked ordinary chondrites as a means of constraining the intensity of any neutron irradiation these meteorites may have experienced.

Walker, R. J.↗

Beta decay of the axially asymmetric ground state of 192 Re

The β decay of 192 75 Re 117 , which lies near the boundary between the regions of predicted prolate and oblate deformations, has been investigated using the KEK Isotope Separation System (KISS) in RIKEN Nishina Center. This is the first case in which a low-energy beam of rhenium isotope has been successfully extracted from an argon gas-stopping cell using a laser-ionization technique, following production via multi-nucleon transfer between heavy ions. The ground state of 192 Re has been assigned J π = (0⁻) based on the observed β feedings and deduced logft values towards the 0⁺ and 2⁺ states in 192 Os, which is known as a typical γ-soft nucleus. Furthermore, the shape transition from axial symmetry to axial asymmetry in the Re isotopes is discussed from the viewpoint of single-particle structure using the nuclear Skyrme-Hartree-Fock model.

192Re↗

Discovery of tantalum, rhenium, osmium, and iridium isotopes

Currently, thirty-eight tantalum, thirty-eight rhenium, thirty-nine osmium, and thirty-eight iridium isotopes have been observed and the discovery of these isotopes is described here. For each isotope a brief synopsis of the first refereed publication, including the production and identification method, is presented.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Nuclear Data Sheets for A=182

Nuclear spectroscopic information for known nuclides of mass number 182 (Lu,Hf,Ta,W,Re,Os,Ir,Pt,Au,Hg, Tl,Pb) with Z=71 to 82 and N=111 to 100 have been evaluated and presented together with adopted energies and J{pi} of levels in these nuclei. No excited state data are yet available for {sup 182}Lu, while only limited structure information is available for {sup 182}Pb and {sup 182}Tl. Rotational band structures are known for {sup 182}Hg and {sup 182}Au but spin-parity assignments remain largely tentative. The decays of {sup 182}Lu, {sup 182}Hg, {sup 182}Au and {sup 182}Tl are not well established. The {sup 182}Hf isotope is of geophysical and astrophysical interest. This evaluation supersedes previous full evaluations of A=182 published by 1988Fi05 and 1975Sc13, and a selected (mainly high-spin) update of A=182 published by 1995Si04.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Structure of the K{sup {pi}=}4{sup +} bands in {sup 186,188}Os

The ({sup 3}He, d) single-proton stripping reaction has been performed on targets of {sup 185,187}Re to investigate the structures of the 4{sub 3}{sup +} states in {sup 186,188}Os. The experiment employed 30 MeV {sup 3}He beams, and the reaction products were analyzed with a Q3D spectrograph. Absolute cross sections were determined at nine angles between 5 deg. and 50 deg. for states up to approximately 3 MeV in excitation energy. Large (5/2){sup +}[402]{sub {pi}+}(3/2){sup +}[402]{sub {pi}}two-quasiparticle components are deduced for the 4{sub 3}{sup +} levels of both isotopes. Their magnitudes are in agreement with calculations performed using the quasiparticle phonon model, which predicts a coexistence of a large hexadecapole with a smaller, but sizable, {gamma}-{gamma} component in the 4{sub 3}{sup +}.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Precision measurements of proton emission from the ground states of {sup 156}Ta and {sup 160}Re

The decays of the {pi}d{sub 3/2} ground states of {sup 156}Ta and {sup 160}Re have been studied in detail using the GREAT spectrometer. More than 7000 {sup 160}Re nuclei were produced in reactions of 290- and 300-MeV {sup 58}Ni ions with an isotopically enriched {sup 106}Cd target and separated in flight using the RITU separator. The proton and {alpha} decays of the {pi}d{sub 3/2} level were confirmed and the half-life and branching ratios of this state were determined with improved precision to be t{sub 1/2}=611{+-}7 {mu}s and b{sub p}=89{+-}1% and b{sub {alpha}=}11{+-}1%, respectively. The {alpha}-decay branch populated the ground state of {sup 156}Ta, allowing improved values for the proton-decay energy and half-life to be obtained (E{sub p}=1011{+-}5 keV; t{sub 1/2}=106{+-}4 ms). The {beta} decay of this level was identified for the first time and a branching ratio of b{sub {beta}=}29{+-}3% was deduced. The spectroscopic factors deduced from these measurements are compared with predictions.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Beyond low beta-decay Q values

Beta decays with low Q values can be utilized in the quest to determine the neutrino mass scale. This is being realized in two experiments, KATRIN and MARE, using tritium and {sup 187}Re, respectively. The beta-decay of {sup 187}Re had the lowest known Q value until 2005, when the beta decay of {sup 115}In to the first excited state of {sup 115}Sn was discovered in Gran Sasso underground laboratory. Last year two independent ion trap measurements confirmed that this decay breaks the former record by an order of magnitude.Our theoretical study on this tiny decay channel complemented the experimental effort by the JYFLTRAP group in Finland and HADES underground laboratory in Belgium. A significant discrepancy between the experimental and theoretical results was found. This might be explained by various atomic contributions known to grow larger as the Q value decreases. However, the traditional recipes for taking these effects into account break down on this new ultra-low Q value regime, providing new challenges for theorists on the borderline between nuclear and atomic physics.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Intense few-cycle hard-UV-pulse-induced internal conversion processes

The internal conversion coefficient for bound-free electron transition of originally energetically forbidden internal conversion processes induced by intense, few-cycle UV laser pulse of Gaussian shape in the case of isomers {sup 107}Ag{sup m} (K shell, E3, 25.47 keV), {sup 90}Nb{sup m} (L{sub 2} shell, M2+E3, 2.3 keV), {sup 183}W{sup m1}(M{sub 5} shell, E2, 1.79 keV), {sup 183}W{sup m2} (N{sub 1} shell, E1, 548 eV), and {sup 188}Re{sup m} (M{sub 2} shell, M3+E4, 2.63 keV), and {sup 235}U{sup m} (O{sub 4} and O{sub 5} shells, E3, 73.5 eV) is determined numerically. Experimental conditions and possibilities of the laser-induced internal conversion process of {sup 183}W{sup m2} from the N{sub 1} shell are discussed in more detail.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Photo-nuclear astrophysics in NewSUBARU {gamma}-ray source

A laser Compton scattering (LCS){gamma}-ray source has been installed at an electron storage ring NewSUBARU at SPring-8. We have studied the nuclear physics using this LCS g-ray source. The half-lives of unstable isotopes, {sup 184}Re and {sup 164}Ho{sup m}, produced by photo-induced reactions have been measured. These half-lives are shorter than previous recommended values by 7% and 3%, respectively. These changes of the half-lives affects to evaluation of cross-sections using the activation method. We have discussed a problem of the residual ratio of an isomer in {sup 180}Ta in supernova explosions. The unstable ground state and the metastable isomer are linked by ({gamma}, {gamma}') reactions. We have developed a new time-dependent model to calculate the isomer ratio in supernovae. The solar abundance of {sup 180}Ta is reproduced by the supernova neutrino process with the present calculated isomer ratio.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

X-Rays Compton Detectors For Biomedical Application

Collimators are usually needed to image sources emitting X-rays that cannot be focused. Alternately, one may employ a Compton Camera (CC) and measure the direction of the incident X-ray by letting it interact with a thin solid, liquid or gaseous material (Tracker) and determine the scattering angle. With respect to collimated cameras, CCs allow higher gamma-ray efficiency in spite of lighter geometry, and may feature comparable spatial resolution. CCs are better when the X-ray energy is high and small setups are required. We review current applications of CCs to Gamma Ray Astronomy and Biomedical systems stressing advantages and drawbacks. As an example, we focus on a particular CC we are developing, which is designed to image small animals administered with marked pharmaceuticals, and assess the bio-distribution and targeting capability of these latter. This camera has to address some requirements: relatively high activity of the imaged objects; detection of gamma-rays of different energies that may range from 140 keV (Tc99m) to 511 keV; presence of gamma and beta radiation with energies up to 2 MeV in case of 188Re. The camera consists of a thin position-sensitive Silicon Drift Detector as Tracker, and a further downstream position-sensitive system employing scintillating crystals and a multi-anode photo-multiplier (Calorimeter). The choice of crystal, pixel size, and detector geometry has been driven by measurements and simulations with the tracking code GEANT4. Spatial resolution, efficiency and scope are discussed.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗

Mechanism of photocatalytic reduction of CO 2 by Re(bpy)(CO) 3 Cl from differences in carbon isotope discrimination

The rhenium complex Re(bpy)(CO) 3 Cl (1, bpy = 2,2'-bipyridine) catalyzes CO 2 reduction to CO in mixtures containing triethanolamine (TEOA) as a sacrificial reductant. The mechanism of this reaction under photocatalytic conditions remains to be fully characterized. Here, we report the competitive carbon kinetic isotope effects ( 13 C KIEs) on photocatalytic CO 2 reduction by 1 and analyze the results of experimental measurements by comparing with computed KIEs via density functional theory (DFT) calculations as a means of formulating a chemical mechanism and illustrating the utility of this approach. The 13 C KIEs, k( 12 C)/k( 13 C), in acetonitrile (ACN) and dimethylformamide (DMF) were determined to be 1.0718 ± 0.0036 and 1.0685 ± 0.0075, respectively. When [Ru(bpy) 3 ]Cl 2 is added to the reaction mixture in acetonitrile as a photosensitizer, the reduction of CO 2 exhibited a 13 C KIE = 1.0703 ± 0.0043. These values are consistent with the calculated isotope effect of CO 2 binding to the one-electron reduced [ReI(bpy• – )(CO) 3 ] species. The findings reported here provide strong evidence that the reactions in the two different solvents have the same first irreversible step and proceed with similar reactive intermediates upon reduction. Theoretically, we found that the major contribution for the large 13 C isotope effects comes from a dominant zero-point energy (ZPE) term. Lastly, these results lay the groundwork for combined experimental and theoretical approaches for analysis of competitive isotope effects toward understanding CO 2 reduction catalyzed by other complexes.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Rhenium-osmium and samarium-neodymium isotopic systematics of the Stillwater complex

The role of magma mixing in the formation of strategic platinum-group element ore deposits is examined using isotopic data from the Stillwater Complex, Montana. Nd and Os isotopic data show that the intrusion formed from at least two distinct magmas: ultramafic (U-type) affinity magmas and anorthositic (A-type) affinity magmas. The U-type magmas formed from a lithospheric mantle source containing recycled crustal materials and the A-type magmas originated either by crustal contamination of basaltic magmas or by partial melting of basalt in the lower crust. The results also suggest that the platinum-group element ore deposits were derived from A-type magmas which were injected into the U-type magma chamber at several stages during the development of the ultramafic series.

Lambert, David D.↗