Temperature-dependent kinetics study of the reactions of O(1D2) with N2 and O2

Literature Information

Publication Date 2004-03-16
DOI 10.1039/B400243A
Impact Factor 3.676
Authors

R. S. Strekowski, J. M. Nicovich


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Abstract

A laser flash photolysis–resonance fluorescence technique has been employed to investigate the kinetics of the reactions of electronically excited oxygen atoms, O(1D2), with N2 (k1) and O2 (k2) as a function of temperature (197–427 K) in helium buffer gas at pressures of 11–40 Torr. The results are well-described by the following Arrhenius expressions (units are 10−11 cm3 molecule−1 s−1): k1(T) = (1.99 ± 0.06) exp{(145 ± 9)/T} and k2(T) = (3.39 ± 0.03) exp{(63 ± 3)/T}. Uncertainties in the Arrhenius parameters are 2σ and represent precision only; estimated accuracies of reported k1(T) and k2(T) values at the 95% confidence level are ±10% around room temperature and ±15% at the temperature extremes of the study. The O(1D2) + O2 kinetic data reported in this study are in very good agreement with available literature values. However, the kinetic data reported in this study (and two other new studies reported in this issue) suggest that the O(1D2) + N2 reaction is significantly faster than previously thought, a finding that has important implications regarding production rates of tropospheric HOx radicals as well as stratospheric HOx and NOx radicals calculated in atmospheric models.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
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Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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