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result(s) for
"X-rays"
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X-ray machines
by
Mattern, Joanne, 1963- author
,
Mattern, Joanne, 1963- How things work
in
X-rays Juvenile literature.
,
Medical radiology Juvenile literature.
,
Medical innovations Juvenile literature.
2016
\"Introduces the reader to x-ray machines.\"-- Provided by publisher.
Calibration and Performance of the REgolith X-Ray Imaging Spectrometer (REXIS) Aboard NASA’s OSIRIS-REx Mission to Bennu
by
Masterson, Rebecca
,
Lim, Lucy F.
,
Bokhour, Ed
in
Aerospace Technology and Astronautics
,
Apollo asteroids
,
Asteroid missions
2021
The REgolith X-ray Imaging Spectrometer (REXIS) instrument on board NASA’s
OSIRIS-REx
mission to the asteroid Bennu is a Class-D student collaboration experiment designed to detect fluoresced X-rays from the asteroid’s surface to measure elemental abundances. In July and November 2019 REXIS collected ∼615 hours of integrated exposure time of Bennu’s sun-illuminated surface from terminator orbits. As reported in Hoak et al. (Results from the REgolith X-ray Imaging Spectrometer (REXIS) at Bennu,
2021
) the REXIS data do not contain a clear signal of X-ray fluorescence from the asteroid, in part due to the low incident solar X-ray flux during periods of observation. To support the evaluation of the upper limits on the detectable X-ray signal that may provide insights for the properties of Bennu’s regolith, we present an overview of the REXIS instrument, its operation, and details of its in-flight calibration on astrophysical X-ray sources. This calibration includes the serendipitous detection of the transient X-ray binary MAXI J0637-430 during Bennu observations, demonstrating the operational success of REXIS at the asteroid. We convey some lessons learned for future X-ray spectroscopy imaging investigations of asteroid surfaces.
Journal Article
Recent advances in battery characterization using in situ XAFS, SAXS, XRD, and their combining techniques: From single scale to multiscale structure detection
2024
Revealing and clarifying the chemical reaction processes and mechanisms inside the batteries will bring a great help to the controllable preparation and performance modulation of batteries. Advanced characterization techniques based on synchrotron radiation (SR) have accelerated the development of various batteries over the past decade. In situ SR techniques have been widely used in the study of electrochemical reactions and mechanisms due to their excellent characteristics. Herein, the three most wide and important synchrotron radiation techniques used in battery research were systematically reviewed, namely X‐ray absorption fine structure (XAFS) spectroscopy, small‐angle X‐ray scattering (SAXS), and X‐ray diffraction (XRD). Special attention is paid to how these characterization techniques are used to understand the reaction mechanism of batteries and improve the practical characteristics of batteries. Moreover, the in situ combining techniques advance the acquisition of single scale structure information to the simultaneous characterization of multiscale structures, which will bring a new perspective to the research of batteries. Finally, the challenges and future opportunities of SR techniques for battery research are featured based on their current development. Advanced characterization techniques contribute to revealing and clarifying the chemical reaction processes and mechanisms inside the batteries. This review comprehensively overviews the recent advances in battery characterization using in situ synchrotron X‐ray absorption fine structure (XAFS), small‐angle X‐ray scattering (SAXS), X‐ray diffraction (XRD), and their combining techniques.
Journal Article
Physicochemical characterization of free troposphere and marine boundary layer ice-nucleating particles collected by aircraft in the eastern North Atlantic
2023
Atmospheric ice nucleation impacts the hydrological cycle and climate by modifying the radiative properties of clouds. To improve our predictive understanding of ice formation, ambient ice-nucleating particles (INPs) need to be collected and characterized. Measurements of INPs at lower latitudes in a remote marine region are scarce. The Aerosol and Cloud Experiments in the Eastern North Atlantic (ACE-ENA) campaign, in the region of the Azores islands, provided the opportunity to collect particles in the marine boundary layer (MBL) and free troposphere (FT) by aircraft during the campaign's summer and winter intensive operation period. The particle population in samples collected was examined by scanning transmission X-ray microscopy with near-edge X-ray absorption fine structure spectroscopy. The identified INPs were analyzed by scanning electron microscopy with energy-dispersive X-ray analysis. We observed differences in the particle population characteristics in terms of particle diversity, mixing state, and organic volume fraction between seasons, mostly due to dry intrusion events during winter, as well as between the sampling locations of the MBL and FT. These differences are also reflected in the temperature and humidity conditions under which water uptake, immersion freezing (IMF), and deposition ice nucleation (DIN) proceed. Identified INPs reflect typical particle types within the particle population on the samples and include sea salt, sea salt with sulfates, and mineral dust, all associated with organic matter, as well as carbonaceous particles. IMF and DIN kinetics are analyzed with respect to heterogeneous ice nucleation rate coefficients, Jhet, and ice nucleation active site density, ns, as a function of the water criterion Δaw. DIN is also analyzed in terms of contact angles following classical nucleation theory. Derived MBL IMF kinetics agree with previous ACE-ENA ground-site INP measurements. FT particle samples show greater ice nucleation propensity compared to MBL particle samples. This study emphasizes that the types of INPs can vary seasonally and with altitude depending on sampling location, thereby showing different ice nucleation propensities, which is crucial information when representing mixed-phase cloud and cirrus cloud microphysics in models.
Journal Article
The BepiColombo Mercury Imaging X-Ray Spectrometer: Science Goals, Instrument Performance and Operations
by
Dennerl, Konrad
,
Tikkanen, Tuomo
,
Genzer, Maria
in
Aerospace environments
,
Aerospace Technology and Astronautics
,
Astrophysics
2020
The Mercury Imaging X-ray Spectrometer is a highly novel instrument that is designed to map Mercury’s elemental composition from orbit at two angular resolutions. By observing the fluorescence X-rays generated when solar-coronal X-rays and charged particles interact with the surface regolith, MIXS will be able to measure the atomic composition of the upper ∼10-20 μm of Mercury’s surface on the day-side. Through precipitating particles on the night-side, MIXS will also determine the dynamic interaction of the planet’s surface with the surrounding space environment.
MIXS is composed of two complementary elements: MIXS-C is a collimated instrument which will achieve global coverage at a similar spatial resolution to that achieved (in the northern hemisphere only – i.e. ∼ 50 – 100 km) by MESSENGER; MIXS-T is the first ever X-ray telescope to be sent to another planet and will, during periods of high solar activity (or intense precipitation of charged particles), reveal the X-ray flux from Mercury at better than 10 km resolution. The design, performance, scientific goals and operations plans of the instrument are discussed, including the initial results from commissioning in space.
Journal Article
Femtosecond x-ray spectroscopy of an electrocyclic ring-opening reaction
by
Schnorr, Kirsten
,
Closser, Kristina D.
,
Attar, Andrew R.
in
Absorption spectra
,
Carbon
,
Chemical bonds
2017
The ultrafast light-activated electrocyclic ring-opening reaction of 1,3-cyclohexadiene is a fundamental prototype of photochemical pericyclic reactions. Generally, these reactions are thought to proceed through an intermediate excited-state minimum (the so-called pericyclic minimum), which leads to isomerization via nonadiabatic relaxation to the ground state of the photoproduct. Here, we used femtosecond (fs) soft x-ray spectroscopy near the carbon K-edge (~284 electron volts) on a table-top apparatus to directly reveal the valence electronic structure of this transient intermediate state. The core-to-valence spectroscopic signature of the pericyclic minimum observed in the experiment was characterized, in combination with time-dependent density functional theory calculations, to reveal overlap and mixing of the frontier valence orbital energy levels. We show that this transient valence electronic structure arises within 60 ± 20 fs after ultraviolet photoexcitation and decays with a time constant of 110 ± 60 fs.
Journal Article