TY - JOUR
T1 - Kinetics and mechanism of the reactions of 2,3-butadione with F and Cl atoms, UV absorption spectra of CH
3
C(O)C(O)CH
2
· and CH
3
C(O)C(O)CH
2
O
2
· radicals, and atmospheric fate of CH
3
C(O)C(O)CH
2
O· radicals
AU - Christensen, L. K.
AU - Sehested, J.
AU - Nielsen, O. J.
AU - Wallington, T. J.
AU - Guschin, A.
AU - Hurley, M. D.
PY - 1998/11/5
Y1 - 1998/11/5
N2 -
FTIR-smog chamber techniques were used to determine rate constants for the gas-phase reaction of Cl and F atoms with CH
3
C(O)C(O)CH
3
and F atoms with CH
3
C(O)F of (4.0 ± 0.5) x 10
-3
, (4.9 ± 0.7) x 10
-11
, and (3.6 ± 0.4) x 10
-12
cm
3
molecule
-1
s
-1
, respectively. Two pathways for the reaction of Cl and F atoms with CH
3
C(O)C(O)CH
3
were found: (1a) Cl + CH
3
C(O)C(O)CH
3
→ HCl + CH
3
C(O)C(O)CH
2
·, (1b) Cl + CH
3
C(O)C(O)CH
3
→ CH
3
C(O)Cl + CH
3
C(O)·, (2a) F + CH
3
C(O)C(O)CH
3
→ HF + CH
3
C(O)C(O)CH
2
·, (2b) F + CH
3
C(O)C(O)CH
3
→ CH
3
C(O)F + CH
3
C(O)·, with branching ratios of k
1b
/(k
1b
+ k
1a
) = 0.23 ± 0.02 and k
2b
/(k
2b
+ k
2a
) = 0.56 ± 0.09. It was determined that the atmospheric fate of CH
3
C(O)C(O)CH
2
O· radicals is decomposition to give HCHO, CO, and CH
3
C(O)· radicals. Pulse radiolysis coupled to UV absorption spectroscopy was used to study the kinetics of the reaction of F atoms with CH
3
C(O)C(O)CH
3
as well as spectra of CH
3
C(O)C(O)CH
2
· and CH
3
C(O)C(O)CH
2
O
2
· radicals over the wavelength range 220-400 nm at 295 K. The rate constant for the reaction of F atoms with CH
3
C(O)C(O)CH
3
was determined to be (4.6 ± 0.8) x 10
-11
cm
3
molecule
-1
s
-1
. The absorption cross sections of CH
3
C(O)C(O)CH
2
and CH
3
C-(O)C(O)CH
2
O
2
· radicals were (5.4 ± 1.0) x 10
-18
at 250 nm and (2.0 ± 0.5) x 10
-18
cm
2
molecule
-1
at 320 nm, respectively. Results are discussed with respect to the available database concerning the reaction of Cl and F atoms with organic compounds.
AB -
FTIR-smog chamber techniques were used to determine rate constants for the gas-phase reaction of Cl and F atoms with CH
3
C(O)C(O)CH
3
and F atoms with CH
3
C(O)F of (4.0 ± 0.5) x 10
-3
, (4.9 ± 0.7) x 10
-11
, and (3.6 ± 0.4) x 10
-12
cm
3
molecule
-1
s
-1
, respectively. Two pathways for the reaction of Cl and F atoms with CH
3
C(O)C(O)CH
3
were found: (1a) Cl + CH
3
C(O)C(O)CH
3
→ HCl + CH
3
C(O)C(O)CH
2
·, (1b) Cl + CH
3
C(O)C(O)CH
3
→ CH
3
C(O)Cl + CH
3
C(O)·, (2a) F + CH
3
C(O)C(O)CH
3
→ HF + CH
3
C(O)C(O)CH
2
·, (2b) F + CH
3
C(O)C(O)CH
3
→ CH
3
C(O)F + CH
3
C(O)·, with branching ratios of k
1b
/(k
1b
+ k
1a
) = 0.23 ± 0.02 and k
2b
/(k
2b
+ k
2a
) = 0.56 ± 0.09. It was determined that the atmospheric fate of CH
3
C(O)C(O)CH
2
O· radicals is decomposition to give HCHO, CO, and CH
3
C(O)· radicals. Pulse radiolysis coupled to UV absorption spectroscopy was used to study the kinetics of the reaction of F atoms with CH
3
C(O)C(O)CH
3
as well as spectra of CH
3
C(O)C(O)CH
2
· and CH
3
C(O)C(O)CH
2
O
2
· radicals over the wavelength range 220-400 nm at 295 K. The rate constant for the reaction of F atoms with CH
3
C(O)C(O)CH
3
was determined to be (4.6 ± 0.8) x 10
-11
cm
3
molecule
-1
s
-1
. The absorption cross sections of CH
3
C(O)C(O)CH
2
and CH
3
C-(O)C(O)CH
2
O
2
· radicals were (5.4 ± 1.0) x 10
-18
at 250 nm and (2.0 ± 0.5) x 10
-18
cm
2
molecule
-1
at 320 nm, respectively. Results are discussed with respect to the available database concerning the reaction of Cl and F atoms with organic compounds.
UR - http://www.scopus.com/inward/record.url?scp=0000226645&partnerID=8YFLogxK
M3 - Journal article
AN - SCOPUS:0000226645
SN - 1089-5639
VL - 102
SP - 8913
EP - 8923
JO - Journal of Physical Chemistry Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory
JF - Journal of Physical Chemistry Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory
IS - 45
ER -