Volume 17, Issue 12 pp. 1281-1297
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Kinetic study of the reaction of OH with HCl from 240–1055 K

A. R. Ravishankara

Corresponding Author

A. R. Ravishankara

Molecular Sciences Branch, Georgia Tech Research Institute, Georgia Institute of Technology, Atlanta, Georgia 30332

Molecular Sciences Branch, Georgia Tech Research Institute, Georgia Institute of Technology, Atlanta, Georgia 30332Search for more papers by this author
P. H. Wine

P. H. Wine

Molecular Sciences Branch, Georgia Tech Research Institute, Georgia Institute of Technology, Atlanta, Georgia 30332

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J. R. Wells

J. R. Wells

Molecular Sciences Branch, Georgia Tech Research Institute, Georgia Institute of Technology, Atlanta, Georgia 30332

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R. L. Thompson

R. L. Thompson

Molecular Sciences Branch, Georgia Tech Research Institute, Georgia Institute of Technology, Atlanta, Georgia 30332

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First published: December 1985
Citations: 41

Abstract

Absolute rate coefficients for the reaction of OH with HCl (k1) have been measured as a function of temperature over the range 240–1055 K. OH was produced by flash photolysis of H2O at λ > 165 nm, 266 nm laser photolysis of O3/H2O mixtures, or 266 nm laser photolysis of H2O2. OH was monitored by time-resolved resonance fluorescenceor pulsed laser–induced fluorescence. In many experiments the HCl concentration was measured in situ in the slow flow reactor by UV photometry. Over the temperature range 240–363 K the following Arrhenius expression is an adequate representation of the data: k1 = (2.4 ± 0.2) × 10−12 exp[−(327 ± 28)/T]cm3 molecule−1 s−1. Over the wider temperature range 240–1055 K, the temperature dependence of k1 deviates from the Arrhenius form, but is adequately described by the expression k1 = 4.5 × 10−17 T1.65 exp(112/T) cm3 molecule−1 s−1. The error in a calculated rate coefficient at any temperature is 20%.

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