Skip to main content
U.S. flag

An official website of the United States government

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Temperature Dependent Kinetics of the OH/HO2/O3 Chain Reaction by Time-Resolved IR Laser Absorption Spectroscopy

Published

Author(s)

S A. Nizkorodov, W W. Harper, B W. Blackmon, David Nesbitt

Abstract

This paper presents an extensive temperature dependent kinetic study of the catalytic HOx ozone cycle, (1) OH + O3 -> O2 and (2) HO2 + O3 -> OH + O2, based on time-resolved, Doppler limited direct absorption spectroscopy of OH with a single mode (δŅ = 0.0001 cm-1) high-resolution infrared laser. The sum of the two chain rate constants, k1 + k2, is measured over the 190-315 K1 + k2, is measured over the 190-315 K temperature range and can be accurately described by an Arrhenius-type expression: k1 + k2 (cm3/s) = 2.26(40) x 10-12 exp[-976(50)/T]. These results are in excellent agreement with studies by Ravishankara et al. [J. Chem. Phys. 1979, 70, 984] and Smith et al. [Int. J. Chem. Kinet. 1984. 16, 41] but are significantly higher than the values currently accepted for atmospheric modeling. In addition, these studies also reflect the first such rate measurements to access the 190-230 K temperature range relevant to kinetic modeling of ozone chain loss in the lower stratosphere.
Citation
Journal of Physical Chemistry A
Volume
104
Issue
No. 17

Keywords

kinetics

Citation

Nizkorodov, S. , Harper, W. , Blackmon, B. and Nesbitt, D. (2000), Temperature Dependent Kinetics of the OH/HO<sub>2</sub>/O<sub>3</sub> Chain Reaction by Time-Resolved IR Laser Absorption Spectroscopy, Journal of Physical Chemistry A (Accessed July 18, 2024)

Issues

If you have any questions about this publication or are having problems accessing it, please contact reflib@nist.gov.

Created April 30, 2000, Updated October 12, 2021