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Proposal for precision determination of 7.8 eV isomeric state in229Th at heavy ion storage ring
<span style="color: rgb(51, 51, 51); font-family: arial, helvetica, sans-serif; font-size: 13px; line-height: 22px; background-color: rgb(248, 248, 248);">The ultraviolet optical transition of the isomeric state in Th-229 has attracted much attention recently due to its potential application to building an atomic/nuclear clock with ultra-high precision. However, the lowest nuclear excitation energy and the lifetime of the first excited state of Th-229 were not measured directly and precisely until now, and how to precisely determine this isomer state of the Th-229 is an urgent requirement. Here an experimental approach of using a technique similar to that of dielectronic recombination to measure the transition energy of the isomer state of Th-229 at heavy ion storage rings is described. It is expected that the resonant transition can be found and determined with a precision better than several milli-eV.</span
Diffusion of Ag, Au and Cs implants in MAX phase Ti3SiC2
MAX phases (M: early transition metal; A: elements in group 13 or 14; X: C or N), such as titanium silicon carbide (Ti3SiC2), have a unique combination of both metallic and ceramic properties, which make them attractive for potential nuclear applications. Ti3SiC2 has been considered as a possible fuel cladding material. This study reports on the diffusivities of fission product surrogates (Ag and Cs) and a noble metal Au (with diffusion behavior similar to Ag) in this ternary compound at elevated temperatures, as well as in dual-phase nanocomposite of Ti3SiC2/3C-SiC and polycrystalline CVD 3C-SiC for behavior comparisons. Samples were implanted with Ag, Au or Cs ions and characterized with various methods, including X-ray diffraction, electron backscatter diffraction, energy dispersive X-ray spectroscopy, Rutherford backscattering spectrometry, helium ion microscopy, and transmission electron microscopy. The results show that in contrast to immobile Ag in 3C-SiC, there is a significant outward diffusion of Ag in Ti3SiC2 within the dual-phase nanocomposite during Ag ion implantation at 873 K. Similar behavior of Au in polycrystalline Ti3SiC2 was also observed. Cs out-diffusion and release from Ti3SiC2 occurred during post-implantation thermal annealing at 973 K. This study suggests caution and further studies in consideration of Ti3SiC2 as a fuel cladding material for advanced nuclear reactors operating at very high temperatures. (C) 2015 Elsevier B.V. All rights reserved
Study of projectile fragmentation reaction with isochronous mass spectrometry
<span style="color: rgb(51, 51, 51); font-family: arial, helvetica, sans-serif; font-size: 13px; line-height: 22px; background-color: rgb(248, 248, 248);">Relative yields of fragments following the Kr-78 projectile fragmentation in a beryllium target were measured in a storage ring by using isochronous mass spectrometry (IMS). Odd-even staggering of the relative fragment yields is observed and can be explained by the odd-even staggering of the particle-emission threshold energies. IMS is a complementary technique to gamma-ray spectroscopy for measuring isomeric ratios, in particular for nuclides with long lifetimes. It was found that the isomeric yield ratios in Fe-53 are almost constant for different longitudinal momenta.</span
Double-peak structures in transmission of H2+ ions through conical multicapillaries in a polymer: Projectile-energy dependence
<span style="color: rgb(51, 51, 51); font-family: arial, helvetica, sans-serif; font-size: 13px; line-height: 22px; background-color: rgb(248, 248, 248);">Transmission experiments of 7-200 keV H-2(+) ions through conical multicapillaries with inlet or outlet diameters of 4/2 mu m and a length of 30 mu m etched in a PC polymer are reported. The yield of the transmitted particles as a function of the capillary tilt angle was measured. The results show that for 200 keV H-2(+) ions the guiding effect disappears but a focusing effect is obtained with a density enhancement factor of 3.5. For 7-50 keV H-2(+) ions their transmitted particle curves exhibit a pair of shoulder peaks on the left-and right-hand side of the center angle 0 degrees. As the ion energy increases, the shoulder-peak structure is found to vanish leaving one peak at 0 degrees.</span
Direct mass measurements of neutron-rich ~(86)Kr projectile fragments and the persistence of neutron magic number N=32 in Sc isotopes
<span style="color: rgb(51, 51, 51); font-family: arial, helvetica, sans-serif; font-size: 13px; line-height: 22px; background-color: rgb(248, 248, 248);">In this paper, we present direct mass measurements of neutron-rich Kr-86 projectile fragments conducted at the HIRFL-CSR facility in Lanzhou by employing the Isochronous Mass Spectrometry (IMS) method. The new mass excesses of 52-54SC nuclides are determined to be -40492(82), -38928(114), -34654(540) keV, which show a significant increase of binding energy compared to the reported ones in the Atomic Mass Evaluation 2012 (AME12). In particular, Sc-53 and Sc-64 are more bound by 0.8 MeV and 1.0 MeV, respectively. The behavior of the two neutron separation energy with neutron numbers indicates a strong sub-shell closure at neutron number N=32 in Sc isotopes.</span