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At least 19 records

Atomic interferometer measurements of Berry and Aharonov-Anandan phases for isolated spins S>(1/2) nonlinearly coupled to external fields

In a recent paper we have studied the peculiar features of the Berry and Aharonov-Anandan geometric phases for isolated spins S{>=}1. We have assumed that they are submitted to a dipole and quadrupole coupling to external E and B fields with the mild restriction E{center_dot}B=0. This implies discrete symmetries leading to remarkable simplifications of the geometry and algebra involved. The aim of the present work is to describe realistic proposals, within the realm of atomic physics, for the verification of some of our most significant theoretical predictions. There are several challenges to be overcome. For alkali-metal atoms, most commonly used in atomic interferometers, the only practical way to generate quadrupole coupling, with a strength comparable to the dipole one, is the ac Stark effect induced by a nearly resonant light beam. One then has to face the instability of the 'dressed' atom hyperfine (hf) level, a candidate for our isolated spin. One deleterious effect is the apparition of an imaginary part in the quadrupole to dipole coupling strength ratio, {lambda}. Fortunately we have found a simple way to get rid of I({lambda}) by an appropriate detuning. We are left with an unstable isolated spin. This implies an upper bound to the quantum cycle duration T{sub c}. In the case of the Berry's phase, T{sub c} has a lower bound due to the necessity of keeping the nonadiabatic corrections below a predefined level. We have found a compromise in the case of the F=2,m=0 {sup 87}Rb ground-state hf level. This is our candidate for the measurement of the somewhat ''exotic'' Berry's phase acquired by the S=2,m=0 state at the end of a quantum cycle involving a rotation of {pi} of the E field--in practice, the linear polarization of the dressing beam --about the B field direction. We have found a way to implement, in a Ramsey-type interferometric measurement, the procedures aimed at controlling the nonadiabatic corrections, as described in detail in our previous theoretical paper. A numerical simulation of our experimental proposal shows that a 0.1% accurate determination of Berry's phase, free of nonadiabatic corrections, can be achieved. Measurements could also be considered for cold {sup 52}Cr chromium atoms with S=3, where values of {lambda}{approx_equal}1 can be obtained with an instability smaller than in the {sup 87}Rb case, due to a more favorable spectroscopic structure. The F=1,m=1 hf level of the {sup 87}Rb ground state offers the opportunity to extend the measurement of Aharonov-Anandan's phases beyond the case S=(1/2). We construct, using 'light shift', the Hamiltonian H{sub ||}(t) generating a closed circuit in the density-matrix space which satisfies at any time the 'parallel transport' condition, thus making the quantum cycle free from the adiabaticity condition. We also consider the case of half-integer spins (e.g., {sup 201}Hg, {sup 135}Ba, and {sup 137}Ba), with their own specific features. We show how the difference of Berry's phases for states S=(3/2) and S=(1/2), with m=(1/2), can be exploited to achieve a holonomic maximum entanglement of three qubits.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Measurement and simulation of the cross sections for nuclide production in {sup 56}Fe and {sup nat}Cr targets irradiated with 0.04- to 2.6-GeV protons

The cross sections for nuclide production in thin {sup 56}Fe and {sup nat}Cr targets irradiated by 0.04-2.6-GeV protons are measured by direct {gamma} spectrometry using two {gamma} spectrometers with the resolutions of 1.8 and 1.7 keV for the {sup 60}Co 1332-keV {gamma} line. As a result, 649 yields of radioactive residual product nuclei have been obtained. The {sup 27}Al(p, x){sup 22}Na reaction has been used as a monitor reaction. The experimental data are compared with the MCNPX (BERTINI, ISABEL), CEM03.02, INCL4.2, INCL4.5, PHITS, and CASCADE07 calculations.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

E6 Gamma Decay

Rare electric hexacontatetrapole (E6) transitions are studied in the full (f{sub 7/2},f{sub 5/2},p{sub 3/2},p{sub 1/2}) shell-model basis. Comparison of theory to the results from the gamma decay in {sup 53}Fe and from inelastic electron scattering on {sup 52}Cr provides unique and interesting tests of the valence wavefunctions, the models used for energy density functionals and into the origin of effective charge.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Spontaneous Demagnetization of a Dipolar Spinor Bose Gas in an Ultralow Magnetic Field

We study the spinor properties of S=3 {sup 52}Cr condensates, in which dipole-dipole interactions allow changes in magnetization. We observe a demagnetization of the Bose-Einstein condensate (BEC) when the magnetic field is quenched below a critical value corresponding to a phase transition between a ferromagnetic and a nonpolarized ground state, which occurs when spin-dependent contact interactions overwhelm the linear Zeeman effect. The critical field is increased when the density is raised by loading the BEC in a deep 2D optical lattice. The magnetization dynamics is set by dipole-dipole interactions.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Cross-sections for (p,x) reactions on natural chromium for the production of 52,52m,54 Mn radioisotopes

The production of positron-emitting isotopes of manganese is potentially important for developing contrast agents for dual-modality positron emission tomography and magnetic resonance (PET/MR) imaging, as well as for in vivo imaging of the biodistribution and toxicity of manganese. Furthermore, the decay properties of 52 Mn make it an excellent candidate for these applications, and it can easily be produced by bombardment of a chromium target with protons or deuterons from a low-energy biomedical cyclotron. There are several parameters essential to this mode of production—target thickness, beam energy, beam current, and bombardment time—depend heavily on the availability of reliable, reproducible cross-section data. Our paper contributes to the routine production of 52g Mn for biomedical research by contributing experimental cross-sections for natural chromium ( nat Cr) targets for the nat Cr(p,x) 52g Mn reaction, as well as for the production of the radiocontaminants 52m, 54 Mn.

07 ISOTOPE AND RADIATION SOURCES↗

Electron screening effect in (p,n) and (p,γ) reactions

To investigate the electron screening effect we compared γ-ray and neutron yields in different metals and insulators (Mn, V and Cd – metals and MnO, VO{sub 2} and CdO – insulators) for the proton induced nuclear reactions {sup 55}Mn(p,n){sup 55}Fe, {sup 55}Mn(p,γ){sup 56}Fe, {sup 113}Cd(p,n){sup 113}In and {sup 51}V(p,γ){sup 52}Cr. We also looked for shifts in resonance energy for metallic compared to insulator targets.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Photon Induced Reaction Cross-Section Calculations of Several Structural Fusion Materials

In this paper; photo-neutron cross-sections have been computed for {sup 27}Al, {sup 28,29}Si, {sup 52}Cr, {sup 54,56}Fe isotopes by using nuclear reaction codes TALYS 1.6 and EMPIRE 3.1 with different level density models. Constant Temperature Fermi Gas, Back Shifted Fermi Gas and Generalized Superfluid Models have been employed from TALYS 1.6 whereas Generalized Super Fluid Model was the only model employed from EMPIRE 3.1 reaction codes. Obtained results have been analyzed with experimental values taken from the EXFOR database.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Stability of a dipolar Bose-Einstein condensate in a one-dimensional lattice

We show that in contrast with contact interacting gases, an optical lattice changes drastically the stability properties of a dipolar condensate, inducing a crossover from dipolar destabilization to dipolar stabilization for increasing lattice depths. Performing stability measurements on a {sup 52}Cr Bose-Einstein condensate in an interaction-dominated regime, repulsive dipolar interaction balances negative scattering lengths down to -17 Bohr radii. Our findings are in excellent agreement with mean-field calculations, revealing the important destabilizing role played by intersite dipolar interactions in deep lattices.

74 ATOMIC AND MOLECULAR PHYSICS↗

Role of break-up processes in the fusion of the {sup 12}C+ {sup 52}Cr system

We present the results and analysis of our investigation of the role of break-up processes on the fusion of a {sup 12}C{sup 6+} beam with a {sup 52}Cr target near, at, and above the Coulomb barrier. In this experiment the excitation functions of evaporation residues produced via ({sup 12}C, 2n), ({sup 12}C, pxn), ({sup 12}C, {alpha}xn), and ({sup 12}C, {alpha}pxn) channels in a {sup 12}C + {sup 52}Cr reaction were measured at several beam energies ranging from {approx_equal}51 to 87 MeV by employing the recoil catcher technique followed by off-line {gamma}-ray spectrometry. The measured excitation functions were compared with theoretical values obtained using the pace4 statistical model code. Further, for a ({sup 12}C, p2n) channel the measured excitation function was compared with the predictions of the alice-91 code, which was chosen as it takes into account pre-equilibrium emissions. For non-{alpha}-emitting channels, the experimentally measured excitation functions--after correcting them for possible contributions from higher charge isobaric precursor decays--were, in general, found to be in good agreement with theoretical predictions. However, for {alpha}-emitting channels, the measured excitation functions had significantly more production cross sections than what pace4 predicted. This enhancement may be attributed to incomplete fusion processes. An attempt was made to estimate the incomplete fusion fraction in order to compare the relative importance of complete and incomplete fusion processes. The incomplete fusion fraction was found to be sensitive to the projectile energy and mass asymmetry of the entrance channel. We also discuss the results in terms of the impact of the frozen {alpha}-cluster structure of the {sup 12}C isotope on various fusion reactions.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

52 Mn Production for PET/MRI Tracking Of Human Stem Cells Expressing Divalent Metal Transporter 1 (DMT1)

There is a growing demand for long-term in vivo stem cell imaging for assessing cell therapy techniques and guiding therapeutic decisions. This work develops the production of 52 Mn and establishes proof of concept for the use of divalent metal transporter 1 (DMT1) as a positron emission tomography (PET) and magnetic resonance imaging (MRI) reporter gene for stem cell tracking in the rat brain. 52 Mn was produced via proton irradiation of a natural chromium target. In a comparison of two 52 Mn separation methods, solvent-solvent extraction was preferred over ion exchange chromatography because of reduced chromium impurities and higher 52 Mn recovery. In vitro uptake of Mn-based PET and MRI contrast agents ( 52 Mn 2+ and Mn 2+ , respectively) was enhanced in DMT1 over-expressing human neural progenitor cells (hNPC-DMT1) compared to wild-type control cells (hNPC-WT). After cell transplantation in the rat striatum, increased uptake of Mn-based contrast agents in grafted hNPC-DMT1 was detected in in vivo manganese-enhanced MRI (MEMRI) and ex vivo PET and autoradiography. These initial studies indicate that this approach holds promise for dual-modality PET/MR tracking of transplanted stem cells in the central nervous system and prompt further investigation into the clinical applicability of this technique.

59 BASIC BIOLOGICAL SCIENCES↗

Characterization of low alloy ferritic steel–Ni base alloy dissimilar metal weld interface by SPM techniques, SEM/EDS, TEM/EDS and SVET

The interface region of welded A508–Alloy 52 M is characterized by scanning probe microscope (SPM) techniques, scanning electron microscopy (SEM)/energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM)/Energy Dispersive Spectroscopy (EDS) and scanning vibrate electrode technique (SVET). The regions along the welded A508–Alloy 52 M interface can be categorized into two types according to their different microstructures. In the type-I interface region, A508 and Alloy 52 M are separated by the fusion boundary, while in the type-II interface region, A508 and Alloy 52 M are separated by a martensite zone. A508, martensite zone and grain boundaries in Alloy 52 M are ferromagnetic while the Alloy 52 M matrix is paramagnetic. The Volta potentials measured by scanning Kelvin probe force microscopy (SKPFM) of A508, martensite zone and Alloy 52 M follow the order: V{sub 52} {sub M} > V{sub A508} > V{sub martensite}. The corrosion behavior of A508–Alloy 52 M interface region is galvanic corrosion, in which Alloy 52 M is cathode while A508 is anode. The martensite dissolves faster than Alloy 52 M, but slower than A508 in the test solution. - Highlights: • The A508–Alloy 52 M interface regions can be categorized into two types. • The chromium depleted region is observed along the Alloy 52 M grain boundary. • The Alloy 52 M grain boundaries which are close to the interface are ferromagnetic. • Martensite zone has lower Volta potential but higher corrosion resistance than A508.

36 MATERIALS SCIENCE↗

Natural and enriched Cr target development for production of Manganese-52

52 Mn is a promising PET radiometal with a half-life of 5.6 days and an average positron energy of 242 keV. Typically, chromium of natural isotope abundance is used as a target material to produce this isotope through the nat/52 Cr(p,n) 52 Mn reaction. While natural Cr is a suitable target material, higher purity 52 Mn could be produced by transitioning to enriched 52 Cr targets to prevent the co-production of long-lived 54 Mn (t 1/2 = 312 day). Unfortunately, 52 Cr targets are not cost-effective without recycling processes in place, therefore, this work aims to explore routes to prepare Cr targets that could be recycled. Natural Cr foils, metal powder pellets, enriched chromium-52 oxide and Cr(III) electroplated targets were investigated in this work. Each of these cyclotron targets were irradiated, and the produced 52 Mn was purified, when possible, using a semi-automated system. An improved purification by solid-phase anion exchange from ethanol-HCl mixtures resulted in recoveries of 94.5 ± 2.2% of 52 Mn. The most promising target configuration to produce a recyclable target was electroplated Cr(III). This work presents several pathways to optimize enriched Cr targets for the production of high purity 52 Mn.

62 RADIOLOGY AND NUCLEAR MEDICINE↗

Isotopic targets with graphene backing

Many of the isotopes cannot be made as free-standing targets and require thin film backing. Low-Z backing materials, such as amorphous carbon and thin polymer films are materials of choice for some experiments. However, the limitations of these backing materials are poor thermal and mechanical stability. All-carbon graphene films would be an excellent choice as a backing material due to their high thermal conductivity, high temperature tolerance (3550ºC melting point), low outgassing, mechanical integrity, and ease of handling. We fabricated a variety of targets using graphene material as a backing or a host matrix. Using PVD sputtering deposition of boron-11 carbide, we fabricated 11 B target with a 0.5 mg/cm 2 on graphene film. The 11 B isotope is of interest due to aneutronic proton–boron fusion reaction 1 p + 11 B → 3 4 He + 8.7 MeV suitable for clean energy production1. We also prepared a neutron rich natCr target on graphene backing by electroplating Cr in an aqueous chromium (III) oxide bath. The chromium target can be used for production of positron emitting Mn radioisotope2 in the reaction 52 Cr (p,n) 52 Mn. One of the unique advantages of the graphene film fabrication process is the capability to embed target materials, including refractory metals, in the nanoparticle form into a host graphene matrix during target preparation. Finally, we fabricated nat Ir, nat Re, nat WO3, and nat HfO 2 nanoparticle-loaded graphene targets that can be used in nuclear physics research.

36 MATERIALS SCIENCE↗

LATERALLY PROPAGATING DETONATIONS IN THIN HELIUM LAYERS ON ACCRETING WHITE DWARFS

Theoretical work has shown that intermediate mass (0.01 M{sub Sun} < M{sub He} < 0.1 M{sub Sun }) helium shells will unstably ignite on the accreting white dwarf (WD) in an AM CVn binary. For more massive (M > 0.8 M{sub Sun }) WDs, these helium shells can be dense enough (>5 Multiplication-Sign 10{sup 5} g cm{sup -3}) that the convectively burning region runs away on a timescale comparable to the sound travel time across the shell, raising the possibility for an explosive outcome rather than an Eddington limited helium novae. The nature of the explosion (i.e., deflagration or detonation) remains ambiguous, is certainly density dependent, and likely breaks spherical symmetry. In the case of detonation, this causes a laterally propagating front whose properties in these geometrically thin and low-density shells we begin to study here. Our calculations show that the radial expansion time of <0.1 s leads to incomplete helium burning, in agreement with recent work by Sim and collaborators, but that the nuclear energy released is still adequate to realize a self-sustaining laterally propagating detonation. These detonations are slower than the Chapman-Jouguet speed of 1.5 Multiplication-Sign 10{sup 9} cm s{sup -1}, but still fast enough at 0.9 Multiplication-Sign 10{sup 9} cm s{sup -1} to go around the star prior to the transit through the star of the inwardly propagating weak shock. Our simulations resolve the subsonic region behind the reaction front in the detonation wave. The two-dimensional nucleosynthesis is shown to be consistent with a truncated one-dimensional Zeldovich-von Neumann-Doering calculation at the slower detonation speed. The ashes from the lateral detonation are typically He rich, and consist of predominantly {sup 44}Ti, {sup 48}Cr, along with a small amount of {sup 52}Fe, with very little {sup 56}Ni and with significant {sup 40}Ca in carbon-enriched layers. If this helium detonation results in a Type Ia supernova, its spectral signatures would appear for the first few days after explosion.

79 ASTRONOMY AND ASTROPHYSICS↗

Chromium speciation and mobility in contaminated coastal urban soils affected by water salinity and redox conditions

Chromium (Cr) is a redox-sensitive element in contaminated coastal urban soils. Sea level rise (SLR) with subsequent soil inundation may facilitate Cr transformation and mobilization through alterations in local redox conditions and porewater ion composition. Here, we investigated the impact of water salinity and redox conditions on Cr chemistry in these environments. Synchrotron-based X-ray spectroscopy and wet chemical analyses revealed that the soils contained very high levels of Cr (up to 4320 mg kg -1 ) and that chromite (~52%) and Fe-Cr hydroxide coprecipitates (~44%) were the predominant Cr species. The abundance of these two components resulted in low Cr mobility under non-flooded conditions. Chromium(II) was identified in the soils, potentially derived from the waste parent material. Seawater and anoxic conditions resulted in lower Cr release compared to freshwater and aerobic conditions. Up to three to eight times more Cr was released under aerobic conditions versus anaerobic conditions in the freshwater versus saltwater, respectively, with total dissolved Cr values remaining below 0.02 mg L -1 . The decrease in Cr release was likely due to Cr reduction by Fe(II) and sulfide. This work provides important information on how salinity and redox fluctuations impact Cr cycling which is likely to occur during SLR.

36 MATERIALS SCIENCE↗

Performance and properties evolution of near-term accident tolerant fuel: Cr-doped UO 2

Chromium-doped UO 2 fuel has received significant interest due to the ability for chromium to produce pellets with large average grain size (>30 μm), which has shown to increase fission gas retention during operation. Sintering of chromium-doped UO 2 pellets was pursued with oxygen potential and sintering atmosphere controlled to tailor the final microstructure of the material. Chromium additions in this study ranged from 750 to 7800 ppm. Cr concentrations were studied pre and post sintering using Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). Effects of chromium content on lattice parameter and microstructure were examined with X-ray diffraction (XRD) and scanning electron microscopy (SEM). Contraction of the UO 2 lattice parameter was observed, as well as enlargement of grain size with increasing chromium content up to 4900 ppm Cr 2 O 3 . In addition, SEM indicated Cr incorporation within the matrix and the formation of chromium oxide precipitates throughout the microstructure at high Cr concentrations. Evaluation of thermophysical properties of Cr-doped UO 2 pellets were conducted up to 1200 °C to illustrate their evolution with increased dopant concentration and microstructural changes. The results show that grain size is maximized at 52 μm with Cr 2 O 3 concentration equal to 4900 ppm; however, grain size decreases at higher Cr 2 O 3 concentrations. No significant changes were observed in specific heat capacity, linear thermal expansion, and coefficient of thermal expansion compared to undoped UO 2 . The thermal conductivity also decreased through the incorporation of Cr 2 O 3 dopants above 750 ppm and is shown to be ~15 % lower than reported UO 2 values.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗

Materials Data on Cr2Cu3(OF)12 by Materials Project

CrF6CrCu3(O2F)6 crystallizes in the triclinic P-1 space group. The structure is three-dimensional and consists of one chromium hexafluoride molecule and one CrCu3(O2F)6 framework. In the CrCu3(O2F)6 framework, Cr is bonded to six F atoms to form CrF6 octahedra that share corners with six CuO4F2 octahedra. The corner-sharing octahedra tilt angles range from 33–52°. There are a spread of Cr–F bond distances ranging from 1.85–1.89 Å. There are three inequivalent Cu sites. In the first Cu site, Cu is bonded to four O and two equivalent F atoms to form CuO4F2 octahedra that share corners with two equivalent CrF6 octahedra. The corner-sharing octahedral tilt angles are 39°. There is two shorter (1.90 Å) and two longer (1.91 Å) Cu–O bond length. Both Cu–F bond lengths are 2.28 Å. In the second Cu site, Cu is bonded to four O and two equivalent F atoms to form CuO4F2 octahedra that share corners with two equivalent CrF6 octahedra. The corner-sharing octahedral tilt angles are 33°. All Cu–O bond lengths are 1.92 Å. Both Cu–F bond lengths are 2.22 Å. In the third Cu site, Cu is bonded to four O and two equivalent F atoms to form CuO4F2 octahedra that share corners with two equivalent CrF6 octahedra. The corner-sharing octahedral tilt angles are 52°. All Cu–O bond lengths are 1.90 Å. Both Cu–F bond lengths are 2.39 Å. There are six inequivalent O sites. In the first O site, O is bonded in a 2-coordinate geometry to one Cu and one O atom. The O–O bond length is 1.29 Å. In the second O site, O is bonded in a 2-coordinate geometry to one Cu and one O atom. In the third O site, O is bonded in a 2-coordinate geometry to one Cu and one O atom. The O–O bond length is 1.29 Å. In the fourth O site, O is bonded in a 2-coordinate geometry to one Cu and one O atom. In the fifth O site, O is bonded in a 2-coordinate geometry to one Cu and one O atom. The O–O bond length is 1.29 Å. In the sixth O site, O is bonded in a 2-coordinate geometry to one Cu and one O atom. There are three inequivalent F sites. In the first F site, F is bonded in a distorted bent 150 degrees geometry to one Cr and one Cu atom. In the second F site, F is bonded in a bent 150 degrees geometry to one Cr and one Cu atom. In the third F site, F is bonded in a distorted bent 120 degrees geometry to one Cr and one Cu atom.

36 MATERIALS SCIENCE↗

DISSOLUTION OF SURROGATE U-Zr FUEL USING ALNIFLEX CONDITIONS

Non-aluminum clad spent nuclear fuel (NASNF) stored in L Basin at the Savannah River Site (SRS) is widely varied in fuel composition, design, packaging, and physical condition. The complexity of the NASNF inventory presents significant challenges, and technology development is necessary for successful disposition. One such fuel in the inventory is metallic uranium-zirconium (U-Zr) alloy fuel, the focus of this study. Electrolytic or nitric acid only dissolution of metallic U-Zr alloy can form insoluble zirconium oxide, which results in up to 52% loss of U to insoluble solids, and can be subject to potentially uncontrolled oxidation reactions [1, 2]. The AlNiflex process was determined to be a viable dissolution flowsheet for the U-Zr alloy fuel. Under a narrow set of solution concentrations, a combination of hydrofluoric acid (HF), nitric acid (HNO3), aluminum nitrate (Al(NO3)3), and hexavalent chromium can safely dissolve U-Zr intermetallic alloys, keep Zr soluble, and not significantly corrode stainless steel (SS) vessels [3, 4.

Gogolski, Jarrod M. [Savannah River National Labor↗