Me. Jenkin et al., KINETIC AND MECHANISTIC STUDY OF THE SELF-REACTION OF CH3OCH2O2 RADICALS AT ROOM-TEMPERATURE, Journal of physical chemistry, 97(45), 1993, pp. 11712-11723
The UV absorption spectrum and kinetics of the self reaction of CH3OCH
2O2 at 298 K have been studied using both the modulated photolysis of
Cl2/CH3OCH3/O2/N2 mixtures and the pulse radiolysis of SF6/CH3OCH3/O2
mixtures. The spectrum, characterized in the range 200-290 nm, is in g
ood agreement with the single published determination.8 The observed s
econd-order removal kinetics of CH3OCH2O2, k5obs, were found to be sen
sitive to both the variation of total pressure (17-760 Torr) and the c
omposition of the reaction mixtures: 2CH3OCH2O2 --> 2CH3OCH2O + O2 (5a
); --> CH3OCHO + CH3OCH2OH + O2 (5b). The kinetic studies and a detail
ed product investigation using long path length FTIR spectroscopy (T =
295 K; Cl2/CH3OCH3/O2/N2 system) provide evidence to support a mechan
ism involving the rapid thermal decomposition of CH3-OCH2O by H atom e
jection occurring in competition with the reaction with O2: CH3OCH2O(M)-->CH3OCHO + H (+M) (6); CH3OCH2O + O2 --> CH3OCHO + HO2 (4). The co
mplications in the measured values of k5obs in the present studies, an
d those reported previously,8 are believed to occur as a direct result
of formation of H atoms from reaction 6. Accordingly, a pressure-inde
pendent value of k5 = (2.1 +/- 0.3) X 10(-12) cm3 molecule-1 s-1 is de
rived for the elementary rate coefficient at 298 K, with identical val
ues of the branching ratio alpha = k5a/k5 = 0.7 +/- 0.1 determined ind
ependently from the FTIR product studies and the modulated photolysis
experiments. As part of this work, the rate coefficient for the reacti
on of Cl atoms with CH3OCH2Cl was found to be (2.9 +/- 0.2) x 10(-11)
cm3 molecule(-1) s-1.