832 research outputs found
Vibration measurement by pulse differential holographic interferometry
Technique measures structural deformation of materials subjected to wide range of temperatures and other environmental conditions. Effects of convection currents are eliminated by operating a pulsed laser in double pulse mode that exposes hologram twice in quick succession
The impact of global nuclear mass model uncertainties on -process abundance predictions
Rapid neutron capture or `-process' nucleosynthesis may be responsible for
half the production of heavy elements above iron on the periodic table. Masses
are one of the most important nuclear physics ingredients that go into
calculations of -process nucleosynthesis as they enter into the calculations
of reaction rates, decay rates, branching ratios and Q-values. We explore the
impact of uncertainties in three nuclear mass models on -process abundances
by performing global monte carlo simulations. We show that root-mean-square
(rms) errors of current mass models are large so that current -process
predictions are insufficient in predicting features found in solar residuals
and in -process enhanced metal poor stars. We conclude that the reduction of
global rms errors below keV will allow for more robust -process
predictions.Comment: 5 pages, 3 figures, invited talk at the 15th International Symposium
on Capture Gamma-Ray Spectroscopy and Related Topics (CGS15), to appear in
EPJ Web of Conference
Applications of holography to vibrations, transient response, and wave propagation
Applications of holography to vibrations, transient response, and wave propagatio
Sensitivity of the r-process to nuclear masses
The rapid neutron capture process (r-process) is thought to be responsible
for the creation of more than half of all elements beyond iron. The scientific
challenges to understanding the origin of the heavy elements beyond iron lie in
both the uncertainties associated with astrophysical conditions that are needed
to allow an r-process to occur and a vast lack of knowledge about the
properties of nuclei far from stability. There is great global competition to
access and measure the most exotic nuclei that existing facilities can reach,
while simultaneously building new, more powerful accelerators to make even more
exotic nuclei. This work is an attempt to determine the most crucial nuclear
masses to measure using an r-process simulation code and several mass models
(FRDM, Duflo-Zuker, and HFB-21). The most important nuclear masses to measure
are determined by the changes in the resulting r-process abundances. Nuclei
around the closed shells near N=50, 82, and 126 have the largest impact on
r-process abundances irrespective of the mass models used.Comment: 5 pages, 4 figures, accepted in European Physical Journal
The sensitivity of r-process nucleosynthesis to the properties of neutron-rich nuclei
About half of the heavy elements in the Solar System were created by rapid
neutron capture, or r-process, nucleosynthesis. In the r-process, heavy
elements are built up via a sequence of neutron captures and beta decays in
which an intense neutron flux pushes material out towards the neutron drip
line. The nuclear network simulations used to test potential astrophysical
scenarios for the r-process therefore require nuclear physics data (masses,
beta decay lifetimes, neutron capture rates, fission probabilities) for
thousands of nuclei far from stability. Only a small fraction of this data has
been experimentally measured. Here we discuss recent sensitivity studies that
aim to determine the nuclei whose properties are most crucial for r-process
calculations.Comment: 8 pages, 4 figures, submitted to the Proceedings of the Fifth
International Conference on Fission and Properties of Neutron-Rich Nuclei
(ICFN5
The impact of individual nuclear properties on -process nucleosynthesis
The astrophysical rapid neutron capture process or ` process' of
nucleosynthesis is believed to be responsible for the production of
approximately half the heavy element abundances found in nature. This
multifaceted problem remains one of the greatest open challenges in all of
physics. Knowledge of nuclear physics properties such as masses, -decay
and neutron capture rates, as well as -delayed neutron emission
probabilities are critical inputs that go into calculations of -process
nucleosynthesis. While properties of nuclei near stability have been
established, much still remains unknown regarding neutron-rich nuclei far from
stability that may participate in the process. Sensitivity studies gauge
the astrophysical response of a change in nuclear physics input(s) which allows
for the isolation of the most important nuclear properties that shape the final
abundances observed in nature. This review summarizes the extent of recent
sensitivity studies and highlights how these studies play a key role in
facilitating new insight into the process. The development of these tools
promotes a focused effort for state-of-the-art measurements, motivates
construction of new facilities and will ultimately move the community towards
addressing the grand challenge of `How were the elements from iron to uranium
made?'.Comment: 60 pages, 20 figures, review articl
Sensitivity studies for r-process nucleosynthesis in three astrophysical scenarios
In rapid neutron capture, or r-process, nucleosynthesis, heavy elements are
built up via a sequence of neutron captures and beta decays that involves
thousands of nuclei far from stability. Though we understand the basics of how
the r-process proceeds, its astrophysical site is still not conclusively known.
The nuclear network simulations we use to test potential astrophysical
scenarios require nuclear physics data (masses, beta decay lifetimes, neutron
capture rates, fission probabilities) for all of the nuclei on the neutron-rich
side of the nuclear chart, from the valley of stability to the neutron drip
line. Here we discuss recent sensitivity studies that aim to determine which
individual pieces of nuclear data are the most crucial for r-process
calculations. We consider three types of astrophysical scenarios: a traditional
hot r-process, a cold r-process in which the temperature and density drop
rapidly, and a neutron star merger trajectory.Comment: 8 pages, 4 figures, submitted to the Proceedings of the International
Nuclear Physics Conference (INPC) 201
Isomerization Mechanism in Hydrazone-Based Rotary Switches: Lateral Shift, Rotation, or Tautomerization?
Two intramolecularly hydrogen-bonded arylhydrazone (aryl = phenyl or naphthyl) molecular switches have been synthesized, and their full and reversible switching between the E and Z configurations have been demonstrated. These chemically controlled configurational rotary switches exist primarily as the E isomer at equilibrium and can be switched to the protonated Z configuration (Z-H^+) by the addition of trifluoroacetic acid. The protonation of the pyridine moiety in the switch induces a rotation around the hydrazone C═N double bond, leading to isomerization. Treating Z-H^+ with base (K_(2)CO_3) yields a mixture of E and “metastable” Z isomers. The latter thermally equilibrates to reinstate the initial isomer ratio. The rate of the Z → E isomerization process showed small changes as a function of solvent polarity, indicating that the isomerization might be going through the inversion mechanism (nonpolar transition state). However, the plot of the logarithm of the rate constant k vs the Dimroth parameter (E_T) gave a linear fit, demonstrating the involvement of a polar transition state (rotation mechanism). These two seemingly contradicting kinetic data were not enough to determine whether the isomerization mechanism goes through the rotation or inversion pathways. The highly negative entropy values obtained for both the forward (E → Z-H^+) and backward (Z → E) processes strongly suggest that the isomerization involves a polarized transition state that is highly organized (possibly involving a high degree of solvent organization), and hence it proceeds via a rotation mechanism as opposed to inversion. Computations of the Z ↔ E isomerization using density functional theory (DFT) at the M06/cc-pVTZ level and natural bond orbital (NBO) wave function analyses have shown that the favorable isomerization mechanism in these hydrogen-bonded systems is hydrazone–azo tautomerization followed by rotation around a C–N single bond, as opposed to the more common rotation mechanism around the C═N double bond
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