Time-resolved fourier transform infrared emission spectroscopy of NH radical in the X<sup>3</sup>Σ<sup>−</sup> ground state
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F22%3A00560210" target="_blank" >RIV/61388955:_____/22:00560210 - isvavai.cz</a>
Výsledek na webu
<a href="https://hdl.handle.net/11104/0333220" target="_blank" >https://hdl.handle.net/11104/0333220</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.jqsrt.2022.108332" target="_blank" >10.1016/j.jqsrt.2022.108332</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Time-resolved fourier transform infrared emission spectroscopy of NH radical in the X<sup>3</sup>Σ<sup>−</sup> ground state
Popis výsledku v původním jazyce
The NH radical is an extremely important specie in nitrogen chemical reaction networks, in the interstellar medium and atmospheric chemistry. Time resolved Fourier transform spectroscopy technique in the frequency range 10–13 µm has been applied for the measurement of a pure rotational spectrum of the NH free radical (NH) in the ground X3Σ− electronic state. Twelve high N (26–29) triplet-resolved pure rotation lines of NH were experimentally observed in the laboratory and compared with satellite ACE (Atmospheric Chemistry Experiment) solar data. In addition, discharge-generated vibration-rotation NH radical bands in the spectral range 1923–3571 cm−1 have been measured with a microsecond time resolution and spectral resolution of 0.02 cm−1. The spectra of the NH radical have been studied in two experimental arrangements. Firstly, in a pulsed positive column discharge of pure hydrogen-nitrogen mixture and secondly, in a discharge of nitrogen-ammonia mixture in the presence of argon buffer gas. Both production methods are described and compared. The population analysis of the experimental spectra was performed via modelling using the accurate MoLLIST line lists for NH. It was shown that laboratory data can be well reproduced by use of a mixture of the local-thermal-equilibrium (LTE) and non-LTE models corresponding to high temperatures (up to 8000 K and up to 6000 K rotational).
Název v anglickém jazyce
Time-resolved fourier transform infrared emission spectroscopy of NH radical in the X<sup>3</sup>Σ<sup>−</sup> ground state
Popis výsledku anglicky
The NH radical is an extremely important specie in nitrogen chemical reaction networks, in the interstellar medium and atmospheric chemistry. Time resolved Fourier transform spectroscopy technique in the frequency range 10–13 µm has been applied for the measurement of a pure rotational spectrum of the NH free radical (NH) in the ground X3Σ− electronic state. Twelve high N (26–29) triplet-resolved pure rotation lines of NH were experimentally observed in the laboratory and compared with satellite ACE (Atmospheric Chemistry Experiment) solar data. In addition, discharge-generated vibration-rotation NH radical bands in the spectral range 1923–3571 cm−1 have been measured with a microsecond time resolution and spectral resolution of 0.02 cm−1. The spectra of the NH radical have been studied in two experimental arrangements. Firstly, in a pulsed positive column discharge of pure hydrogen-nitrogen mixture and secondly, in a discharge of nitrogen-ammonia mixture in the presence of argon buffer gas. Both production methods are described and compared. The population analysis of the experimental spectra was performed via modelling using the accurate MoLLIST line lists for NH. It was shown that laboratory data can be well reproduced by use of a mixture of the local-thermal-equilibrium (LTE) and non-LTE models corresponding to high temperatures (up to 8000 K and up to 6000 K rotational).
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10403 - Physical chemistry
Návaznosti výsledku
Projekt
<a href="/cs/project/EF16_019%2F0000778" target="_blank" >EF16_019/0000778: Centrum pokročilých aplikovaných přírodních věd</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2022
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Quantitative Spectroscopy and Radiative Transfer
ISSN
0022-4073
e-ISSN
1879-1352
Svazek periodika
291
Číslo periodika v rámci svazku
NOV 2022
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
9
Strana od-do
108332
Kód UT WoS článku
000866229700006
EID výsledku v databázi Scopus
2-s2.0-85135587615