TY - JOUR
T1 - Pressure dependence of the rate coefficients and product yields for the reaction of CH3CO radicals with O2
AU - Tyndall, Geoffrey S.
AU - Orlando, John J.
AU - Wallington, Timothy J.
AU - Hurley, Michael D.
PY - 1997
Y1 - 1997
N2 - Relative rate coefficients for the reaction of acetyl (CH3CO) radicals with O2 (k4) and Cl2 (k7,) have been obtained at 298 K and 228 K as a function of total pressure, using FTIR/environmental chamber techniques. Measured values of k4/k7 were placed on an absolute basis using k7 = 2.8 × 10-11 exp(-47/T) cm3 molec-1 s-1. At 298 K, the value of k4 is constant ((7 ± 2) × 10-13 cm3 molec-1 s-1) at pressures from 0.1 to 2 torr, then increases to a high pressure limiting value of (3.2 ± 0.6) × 10-12 cm3 molec-1 s-1. which is approached at pressures above 300 torr. At 228 K, the low-pressure value of k4 increases by about 20-30% while the high pressure value remains unchanged. Experiments designed to elucidate the products of reaction (4) as a function of pressure at 298 K indicate that the reaction occurs via a concerted mechanism in which CH3CO radicals combine with O2 to give an excited acetylperoxy radical (CH3COO2*) which is increasingly stabilized at high pressure at the expense of a low pressure decomposition channel. The yield of acetylperoxy radicals from reaction (4) decreases from >95% at pressures above 100 torr, to about 90% at 60 torr, and 50% at 6 torr. Indirect evidence for formation of OH radicals from the low pressure decomposition is presented, although the carbon-containing coproduct(s) of this channel could not be identified.
AB - Relative rate coefficients for the reaction of acetyl (CH3CO) radicals with O2 (k4) and Cl2 (k7,) have been obtained at 298 K and 228 K as a function of total pressure, using FTIR/environmental chamber techniques. Measured values of k4/k7 were placed on an absolute basis using k7 = 2.8 × 10-11 exp(-47/T) cm3 molec-1 s-1. At 298 K, the value of k4 is constant ((7 ± 2) × 10-13 cm3 molec-1 s-1) at pressures from 0.1 to 2 torr, then increases to a high pressure limiting value of (3.2 ± 0.6) × 10-12 cm3 molec-1 s-1. which is approached at pressures above 300 torr. At 228 K, the low-pressure value of k4 increases by about 20-30% while the high pressure value remains unchanged. Experiments designed to elucidate the products of reaction (4) as a function of pressure at 298 K indicate that the reaction occurs via a concerted mechanism in which CH3CO radicals combine with O2 to give an excited acetylperoxy radical (CH3COO2*) which is increasingly stabilized at high pressure at the expense of a low pressure decomposition channel. The yield of acetylperoxy radicals from reaction (4) decreases from >95% at pressures above 100 torr, to about 90% at 60 torr, and 50% at 6 torr. Indirect evidence for formation of OH radicals from the low pressure decomposition is presented, although the carbon-containing coproduct(s) of this channel could not be identified.
UR - https://www.scopus.com/pages/publications/0031236586
U2 - 10.1002/(SICI)1097-4601(1997)29:9<655::AID-KIN2>3.0.CO;2-T
DO - 10.1002/(SICI)1097-4601(1997)29:9<655::AID-KIN2>3.0.CO;2-T
M3 - Article
AN - SCOPUS:0031236586
SN - 0538-8066
VL - 29
SP - 655
EP - 663
JO - International Journal of Chemical Kinetics
JF - International Journal of Chemical Kinetics
IS - 9
ER -