4,866 research outputs found

    Measurement of neutron capture on 48^{48}Ca at thermal and thermonuclear energies

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    At the Karlsruhe pulsed 3.75\,MV Van de Graaff accelerator the thermonuclear 48^{48}Ca(n,γ\gamma)49^{49}Ca(8.72\,min) cross section was measured by the fast cyclic activation technique via the 3084.5\,keV γ\gamma-ray line of the 49^{49}Ca-decay. Samples of CaCO3_3 enriched in 48^{48}Ca by 77.87\,\% were irradiated between two gold foils which served as capture standards. The capture cross-section was measured at the neutron energies 25, 151, 176, and 218\,keV, respectively. Additionally, the thermal capture cross-section was measured at the reactor BR1 in Mol, Belgium, via the prompt and decay γ\gamma-ray lines using the same target material. The 48^{48}Ca(n,γ\gamma)49^{49}Ca cross-section in the thermonuclear and thermal energy range has been calculated using the direct-capture model combined with folding potentials. The potential strengths are adjusted to the scattering length and the binding energies of the final states in 49^{49}Ca. The small coherent elastic cross section of 48^{48}Ca+n is explained through the nuclear Ramsauer effect. Spectroscopic factors of 49^{49}Ca have been extracted from the thermal capture cross-section with better accuracy than from a recent (d,p) experiment. Within the uncertainties both results are in agreement. The non-resonant thermal and thermonuclear experimental data for this reaction can be reproduced using the direct-capture model. A possible interference with a resonant contribution is discussed. The neutron spectroscopic factors of 49^{49}Ca determined from shell-model calculations are compared with the values extracted from the experimental cross sections for 48^{48}Ca(d,p)49^{49}Ca and 48^{48}Ca(n,γ\gamma)49^{49}Ca.Comment: 15 pages (uses Revtex), 7 postscript figures (uses psfig), accepted for publication in PRC, uuencoded tex-files and postscript-files also available at ftp://is1.kph.tuwien.ac.at/pub/ohu/Ca.u

    Dependence of direct neutron capture on nuclear-structure models

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    The prediction of cross sections for nuclei far off stability is crucial in the field of nuclear astrophysics. We calculate direct neutron capture on the even-even isotopes 124145^{124-145}Sn and 208238^{208-238}Pb with energy levels, masses, and nuclear density distributions taken from different nuclear-structure models. The utilized structure models are a Hartree-Fock-Bogoliubov model, a relativistic mean field theory, and a macroscopic-microscopic model based on the finite-range droplet model and a folded-Yukawa single-particle potential. Due to the differences in the resulting neutron separation and level energies, the investigated models yield capture cross sections sometimes differing by orders of magnitude. This may also lead to differences in the predicted astrophysical r-process paths. Astrophysical implications are discussed.Comment: 25 pages including 12 figures, RevTeX, to appear in Phys. Rev.

    Muon Catalyzed Fusion in 3 K Solid Deuterium

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    Muon catalyzed fusion in deuterium has traditionally been studied in gaseous and liquid targets. The TRIUMF solid-hydrogen-layer target system has been used to study the fusion reaction rates in the solid phase of D_2 at a target temperature of 3 K. Products of two distinct branches of the reaction were observed; neutrons by a liquid organic scintillator, and protons by a silicon detector located inside the target system. The effective molecular formation rate from the upper hyperfine state of μd\mu d and the hyperfine transition rate have been measured: λ~(3/2)=2.71(7)stat.(32)syst.μ/s\tilde{\lambda}_(3/2)=2.71(7)_{stat.}(32)_{syst.} \mu/s, and λ~(3/2)(1/2)=34.2(8)stat.(1)syst.μ/s\tilde{\lambda}_{(3/2)(1/2)} =34.2(8)_{stat.}(1)_{syst.} \mu /s. The molecular formation rate is consistent with other recent measurements, but not with the theory for isolated molecules. The discrepancy may be due to incomplete thermalization, an effect which was investigated by Monte Carlo calculations. Information on branching ratio parameters for the s and p wave d+d nuclear interaction has been extracted.Comment: 19 pages, 11 figures, submitted to PRA Feb 20, 199

    Measurement of the Resonant dμtd\mu t Molecular Formation Rate in Solid HD

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    Measurements of muon-catalyzed dt fusion (dμt4He+n+μd\mu t \to ^4He+n+\mu^-) in solid HD have been performed. The theory describing the energy dependent resonant molecular formation rate for the reaction μt\mu t + HD [(dμt)pee]\to [(d\mu t)pee]^* is compared to experimental results in a pure solid HD target. Constraints on the rates are inferred through the use of a Monte Carlo model developed specifically for the experiment. From the time-of- flight analysis of fusion events in 16 and 37 μgcm2\mu g\cdot cm^{-2} targets, an average formation rate consistent with 0.897±\pm(0.046)stat±_{stat}\pm (0.166)syst_{syst} times the theoretical prediction was obtained.Comment: 4 pages, 5 figure

    Resonant Formation of dμtd\mu t Molecules in Deuterium: An Atomic Beam Measurement of Muon Catalyzed dt Fusion

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    Resonant formation of dμtd\mu t molecules in collisions of muonic tritium (μt\mu t) on D2_2 was investigated using a beam of μt\mu t atoms, demonstrating a new direct approach in muon catalyzed fusion studies. Strong epithermal resonances in dμtd\mu t formation were directly revealed for the first time. From the time-of-flight analysis of 2036±1162036\pm 116 dtdt fusion events, a formation rate consistent with 0.73±(0.16)meas±(0.09)model0.73\pm (0.16)_{meas} \pm (0.09)_{model} times the theoretical prediction was obtained. For the largest peak at a resonance energy of 0.423±0.0370.423 \pm 0.037 eV, this corresponds to a rate of (7.1±1.8)×109(7.1 \pm 1.8) \times 10^9 s1^{-1}, more than an order of magnitude larger than those at low energies.Comment: To appear in Phys. Rev. Let

    Quantitative analysis of powder mixtures by raman spectrometry : the influence of particle size and its correction

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    Particle size distribution and compactness have significant confounding effects on Raman signals of powder mixtures, which cannot be effectively modeled or corrected by traditional multivariate linear calibration methods such as partial least-squares (PLS), and therefore greatly deteriorate the predictive abilities of Raman calibration models for powder mixtures. The ability to obtain directly quantitative information from Raman signals of powder mixtures with varying particle size distribution and compactness is, therefore, of considerable interest In this study, an advanced quantitative Raman calibration model was developed to explicitly account for the confounding effects of particle size distribution and compactness on Raman signals of powder mixtures. Under the theoretical guidance of the proposed Raman calibration model, an advanced dual calibration strategy was adopted to separate the Raman contributions caused by the changes in mass fractions of the constituents in powder mixtures from those induced by the variations in the physical properties of samples, and hence achieve accurate quantitative determination for powder mixture samples. The proposed Raman calibration model was applied to the quantitative analysis of backscatter Raman measurements of a proof-of-concept model system of powder mixtures consisting of barium nitrate and potassium chromate. The average relative prediction error of prediction obtained by the proposed Raman calibration model was less than one-third of the corresponding value of the best performing PLS model for mass fractions of barium nitrate in powder mixtures with variations in particle size distribution, as well as compactness
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