Experimental Study of the Reaction of O( 3 P) with Carbonyl Sulfide between 220 and 960 K.

The reaction of a ground-state O atom with carbonyl sulfide is of interest for atmospheric (stratosphere and hot near-source volcanic plume) and combustion chemistry. In the present work, we employed a discharge-flow system combined with a modulated molecular beam mass spectrometry technique to measure the rate constant and products of the O + OCS reaction. The overall rate constant was determined either from the kinetics of the reaction product, SO radical, formation or under pseudo-first-order conditions from the decays of OCS in an excess of oxygen atoms: k 1 = 1.92 × 10 -12 × ( T /298) 2.08  exp(-1524/ T ) cm 3 molecule -1 s -1 at T = 220-960 K, with conservative uncertainty of 20%. The yield of another reaction product, CO 2 , was found to increase from 3.55% at T = 455 K to 14.2% at T = 960 K, resulting in the following Arrhenius expression for the rate constant of the minor (S + CO 2 forming) reaction channel: k 1b = 4.19 × 10 -11  exp(-4088/ T ) cm 3 molecule -1 s -1 at T = 455-960 K (with an uncertainty of 25%). The kinetic and mechanistic data from the present work are discussed in comparison with previous experimental and computational studies.