Kinetic Study of the Reactions of Ground State Atomic Carbon and Oxygen with Nitrogen Dioxide over the 50–296 K Temperature Range

The kinetics of the reactions of nitrogen dioxide, NO<sub>2</sub>, with atomic oxygen and atomic carbon in their ground triplet states (<sup>3</sup>P) have been studied at room temperature and below using a supersonic flow (Laval nozzle) reactor. O(<sup>3</sup>P) and C(<sup>3</sup>P) atoms (hereafter O and C respectively) were created in situ by the pulsed laser photolysis of the precursor molecules NO<sub>2</sub> at 355 nm and CBr<sub>4</sub> at 266 nm, respectively. While the progress of the O + NO<sub>2</sub> reaction was followed by detecting O atoms by a chemiluminescent tracer method, progress of the C + NO<sub>2</sub> reaction was followed by detecting C atoms directly by vacuum ultraviolet laser-induced fluorescence at 116 nm. The measured rate constants for the O + NO<sub>2</sub> reaction are found to be in excellent agreement with earlier work at higher temperatures and extend the available kinetic data for this process down to 50 K. The present work represents the first kinetics study of the C + NO<sub>2</sub> reaction. Although both reactions display rate constants that increase as the temperature falls, a more substantial rate increase is observed for the O + NO<sub>2</sub> reaction. The effects of these reactions on the simulated abundances of interstellar NO<sub>2</sub> and related compounds were tested using a gas-grain model of the dense interstellar medium, employing expressions for the rate constants of the form, <i>k</i>(<i>T</i>) = α(<i>T</i>/300)<sup>β</sup>, with α = 1 × 10<sup>-11</sup> cm<sup>3</sup> s<sup>-1</sup> and β = -0.65 for the O + NO<sub>2</sub> reaction and α = 2 × 10<sup>-10</sup> cm<sup>3</sup> s<sup>-1</sup> and β = -0.11 for the C + NO<sub>2</sub> reaction. Although these simulations predict that gas-phase NO<sub>2</sub> abundances are low in dense interstellar clouds, NO<sub>2</sub> abundances on interstellar dust grains are predicted to reach reasonably high levels, indicating the potential for detection of this species in warmer regions.

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Publication Details

Journal
The Journal of Physical Chemistry A
Published
2024-11-26
DOI
https://doi.org/10.1021/acs.jpca.4c06193
Citations
2
Primary Topic
Atmospheric Ozone and Climate
Type
article
Field-Weighted Citation Impact
0.75

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article

Kinetic Study of the Reactions of Ground State Atomic Carbon and Oxygen with Nitrogen Dioxide over the 50–296 K Temperature Range

Jean‐Christophe Loison, Kevin M. Hickson
2 citations
The Journal of Physical Chemistry A
Atmospheric Ozone and Climate
0.75
article

Kinetic Study of the Reactions of Ground State Atomic Carbon and Oxygen with Nitrogen Dioxide over the 50–296 K Temperature Range

Jean‐Christophe Loison, Kevin M. Hickson
article en
2 citations

Abstract

The kinetics of the reactions of nitrogen dioxide, NO<sub>2</sub>, with atomic oxygen and atomic carbon in their ground triplet states (<sup>3</sup>P) have been studied at room temperature and below using a supersonic flow (Laval nozzle) reactor. O(<sup>3</sup>P) and C(<sup>3</sup>P) atoms (hereafter O and C respectively) were created in situ by the pulsed laser photolysis of the precursor molecules NO<sub>2</sub> at 355 nm and CBr<sub>4</sub> at 266 nm, respectively. While the progress of the O + NO<sub>2</sub> reaction was followed by detecting O atoms by a chemiluminescent tracer method, progress of the C + NO<sub>2</sub> reaction was followed by detecting C atoms directly by vacuum ultraviolet laser-induced fluorescence at 116 nm. The measured rate constants for the O + NO<sub>2</sub> reaction are found to be in excellent agreement with earlier work at higher temperatures and extend the available kinetic data for this process down to 50 K. The present work represents the first kinetics study of the C + NO<sub>2</sub> reaction. Although both reactions display rate constants that increase as the temperature falls, a more substantial rate increase is observed for the O + NO<sub>2</sub> reaction. The effects of these reactions on the simulated abundances of interstellar NO<sub>2</sub> and related compounds were tested using a gas-grain model of the dense interstellar medium, employing expressions for the rate constants of the form, <i>k</i>(<i>T</i>) = α(<i>T</i>/300)<sup>β</sup>, with α = 1 × 10<sup>-11</sup> cm<sup>3</sup> s<sup>-1</sup> and β = -0.65 for the O + NO<sub>2</sub> reaction and α = 2 × 10<sup>-10</sup> cm<sup>3</sup> s<sup>-1</sup> and β = -0.11 for the C + NO<sub>2</sub> reaction. Although these simulations predict that gas-phase NO<sub>2</sub> abundances are low in dense interstellar clouds, NO<sub>2</sub> abundances on interstellar dust grains are predicted to reach reasonably high levels, indicating the potential for detection of this species in warmer regions.

The Journal of Physical Chemistry AVol. 128(49)
Centre National de la Recherche Scientifique (FR), Université de Bordeaux (FR), Institut des Sciences Moléculaires (FR), Institut Polytechnique de Bordeaux (FR)
Centre National d’Etudes Spatiales, Centre National de la Recherche Scientifique, Commissariat à l'Énergie Atomique et aux Énergies Alternatives
Openalex Percentile: Top 29%
Atmospheric Ozone and Climate
0.75
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