The determinations of rate constants for the reactions de Cl atoms with organic
compounds could show discrepancy when they are carried out in N2 or air as the diluent
gas. Kaiser and Wallington [1] discovered that the apparent rate constant of reaction C2H4 + Cl ¨ Products increased when the amount of O2 in the diluent gas was raised.
They observed that O2 affected the measured rate constant indicated that reactions of
C2H4 with radicals other than Cl may occur at low pressures in their relative rate
determinations, leading to erroneous results in the presence of O2. In agreement with
Michael et al. [2] and Tyndall et al. [3], Kaiser and Wallington indicated that the
potential interference is OH radical formed via secondary reactions involving O2 and
that the magnitude of this interference may depend on the total pressure and on the initial reactant concentrations.
gas. Kaiser and Wallington [1] discovered that the apparent rate constant of reaction
C2H4 + Cl ¨ Products increased when the amount of O2 in the diluent gas was raised.
They observed that O2 affected the measured rate constant indicated that reactions of
C2H4 with radicals other than Cl may occur at low pressures in their relative rate
determinations, leading to erroneous results in the presence of O2. In agreement with
Michael et al. [2] and Tyndall et al. [3], Kaiser and Wallington indicated that the
potential interference is OH radical formed via secondary reactions involving O2 and
that the magnitude of this interference may depend on the total pressure and on the initial reactant concentrations.
They observed that O2 affected the measured rate constant indicated that reactions of
C2H4 with radicals other than Cl may occur at low pressures in their relative rate
determinations, leading to erroneous results in the presence of O2. In agreement with
Michael et al. [2] and Tyndall et al. [3], Kaiser and Wallington indicated that the
potential interference is OH radical formed via secondary reactions involving O2 and
that the magnitude of this interference may depend on the total pressure and on the initial reactant concentrations.
C2H4 with radicals other than Cl may occur at low pressures in their relative rate
determinations, leading to erroneous results in the presence of O2. In agreement with
Michael et al. [2] and Tyndall et al. [3], Kaiser and Wallington indicated that the
potential interference is OH radical formed via secondary reactions involving O2 and
that the magnitude of this interference may depend on the total pressure and on the initial reactant concentrations.
determinations, leading to erroneous results in the presence of O2. In agreement with
Michael et al. [2] and Tyndall et al. [3], Kaiser and Wallington indicated that the
potential interference is OH radical formed via secondary reactions involving O2 and
that the magnitude of this interference may depend on the total pressure and on the initial reactant concentrations.
Michael et al. [2] and Tyndall et al. [3], Kaiser and Wallington indicated that the
potential interference is OH radical formed via secondary reactions involving O2 and
that the magnitude of this interference may depend on the total pressure and on the initial reactant concentrations.
potential interference is OH radical formed via secondary reactions involving O2 and
that the magnitude of this interference may depend on the total pressure and on the initial reactant concentrations.
that the magnitude of this interference may depend on the total pressure and on the
initial reactant concentrations.