scholarly journals Measuring Neptunium Concentration using Optical Spectrometry for the Pu-238 Supply Program

2021 ◽  
Author(s):  
Luke Sadergaski ◽  
Kaara Patton ◽  
Gretchen Toney ◽  
David DePaoli ◽  
Laetitia Delmau
Keyword(s):  
Photonics ◽  
2021 ◽  
Vol 8 (6) ◽  
pp. 192
Author(s):  
Theocharis Lamprou ◽  
Rodrigo Lopez-Martens ◽  
Stefan Haessler ◽  
Ioannis Liontos ◽  
Subhendu Kahaly ◽  
...  

Quantum-optical spectrometry is a recently developed shot-to-shot photon correlation-based method, namely using a quantum spectrometer (QS), that has been used to reveal the quantum optical nature of intense laser–matter interactions and connect the research domains of quantum optics (QO) and strong laser-field physics (SLFP). The method provides the probability of absorbing photons from a driving laser field towards the generation of a strong laser–field interaction product, such as high-order harmonics. In this case, the harmonic spectrum is reflected in the photon number distribution of the infrared (IR) driving field after its interaction with the high harmonic generation medium. The method was implemented in non-relativistic interactions using high harmonics produced by the interaction of strong laser pulses with atoms and semiconductors. Very recently, it was used for the generation of non-classical light states in intense laser–atom interaction, building the basis for studies of quantum electrodynamics in strong laser-field physics and the development of a new class of non-classical light sources for applications in quantum technology. Here, after a brief introduction of the QS method, we will discuss how the QS can be applied in relativistic laser–plasma interactions and become the driving factor for initiating investigations on relativistic quantum electrodynamics.


Sensors ◽  
2018 ◽  
Vol 18 (7) ◽  
pp. 2001 ◽  
Author(s):  
Marcin Marzejon ◽  
Monika Kosowska ◽  
Daria Majchrowicz ◽  
Barbara Bułło-Piontecka ◽  
Michał Wąsowicz ◽  
...  

2018 ◽  
Vol 54 (1) ◽  
pp. 57-85 ◽  
Author(s):  
Xinrong Xu ◽  
Jingjun Zhong ◽  
Yingying Su ◽  
Zhirong Zou ◽  
Yaqin He ◽  
...  

2020 ◽  
Vol 74 (5) ◽  
pp. 563-570 ◽  
Author(s):  
Wangquan Ye ◽  
Jinjia Guo ◽  
Nan Li ◽  
Fujun Qi ◽  
Kai Cheng ◽  
...  

Depth profiling investigation plays an important role in studying the dynamic processes of the ocean. In this paper, a newly developed hyphenated underwater system based on multi-optical spectrometry is introduced and used to measure seawater spectra at different depths with the aid of a remotely operated vehicle (ROV). The hyphenated system consists of two independent compact deep-sea spectral instruments, a deep ocean compact autonomous Raman spectrometer and a compact underwater laser-induced breakdown spectroscopy system for sea applications (LIBSea). The former was used to take both Raman scattering and fluorescence of seawater, and the LIBS signal could be recorded with the LIBSea. The first sea trial of the developed system was taken place in the Bismarck Sea, Papua New Guinea, in June 2015. Over 4000 multi-optical spectra had been captured up to the diving depth about 1800 m at maximum. The depth profiles of some ocean parameters were extracted from the captured joint Raman–fluorescence and LIBS spectra with a depth resolution of 1 m. The concentrations of [Formula: see text] and the water temperatures were measured using Raman spectra. The fluorescence intensities from both colored dissolved organic matter (CDOM) and chlorophyll were found to be varied in the euphotic zone. With LIBS spectra, the depth profiles of metallic elements were also obtained. The normalized intensity of atomic line Ca(I) extracted from LIBS spectra raised around the depth of 1600 m, similar to the depth profile of CDOM. This phenomenon might be caused by the nonbuoyant hydrothermal plumes. It is worth mentioning that this is the first time Raman and LIBS spectroscopy have been applied simultaneously to the deep-sea in situ investigations.


2018 ◽  
Vol 125 (6) ◽  
pp. 858-863
Author(s):  
P. A. Dement’ev ◽  
M. S. Dunaevskii ◽  
L. B. Matyushkin ◽  
A. V. Nezhdanov ◽  
A. N. Smirnov ◽  
...  

1981 ◽  
Vol 35 (4) ◽  
pp. 380-384 ◽  
Author(s):  
Robert S. Houk ◽  
Harry J. Svec ◽  
Velmer A. Fassel

Mass spectra have been obtained of species in the axial channel of an inductively coupled argon plasma by extracting ions from the inductively coupled plasma into a vacuum system housing a quadrupole mass spectrometer. Ionization temperatures ( Tion) are obtained from relative count rates of m/z-resolved ions according to two general types of ionization equilibrium considerations: (a) the ratio of doubly/singly charged ions of the same element, and (b) the ratio of singly charged ions from two elements of different ionization energy. The Tion values derived from measurement of Ar+2/Ar+, Ba+2/Ba+, Sr+2/Sr+, and Cd+/I+ are all greater than those expected from excitation temperatures measured by other workers. The latter three values for Tion are in reasonable agreement with values obtained by optical spectrometry for a variety of argon inductively coupled plasmas.


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