scholarly journals Understanding the kinetics of the ClO dimer cycle

2006 ◽  
Vol 6 (4) ◽  
pp. 7905-7944 ◽  
Author(s):  
M. von Hobe ◽  
R. J. Salawitch ◽  
T. Canty ◽  
H. Keller-Rudek ◽  
G. K. Moortgat ◽  
...  

Abstract. Among the major factors controlling ozone loss in the polar winter is the kinetics of the ClO dimer catalytic cycle. The most important issues are the thermal equilibrium between ClO and Cl2O2, the rate of Cl2O2 formation, and the Cl2O2 photolysis rate. All these issues have been addressed in a large number of laboratory, field and theoretical studies, but large discrepancies between individual results exist and a self-consistent set of parameters compatible with field observations of ClO and Cl2O2 has not been identified. Here, we use thermodynamic calculations and unimolecular rate theory to constrain the ClO/Cl2O2 equilibrium constant and the rate constants for Cl2O2 formation and dissociation. This information is used together with available atmospheric data to examine Cl2O2 photolysis rates based on different Cl2O2 absorption cross sections. Good overall consistency is achieved using a ClO/Cl2O2 equilibrium constant recently suggested by Plenge et al. (2005), the Cl2O2 recombination rate constant reported by Nickolaisen et al. (1994) and Cl2O2 photolysis rates based on averaged absorption cross sections that are roughly intermediate between the JPL 2002 assessment and a laboratory study by Burkholder et al. (1990).

2007 ◽  
Vol 7 (12) ◽  
pp. 3055-3069 ◽  
Author(s):  
M. von Hobe ◽  
R. J. Salawitch ◽  
T. Canty ◽  
H. Keller-Rudek ◽  
G. K. Moortgat ◽  
...  

Abstract. Among the major factors controlling ozone loss in the polar vortices in winter/spring is the kinetics of the ClO dimer catalytic cycle. Here, we propose a strategy to test and improve our understanding of these kinetics by comparing and combining information on the thermal equilibrium between ClO and Cl2O2, the rate of Cl2O2 formation, and the Cl2O2 photolysis rate from laboratory experiments, theoretical studies and field observations. Concordant with a number of earlier studies, we find considerable inconsistencies of some recent laboratory results with rate theory calculations and stratospheric observations of ClO and Cl2O2. The set of parameters for which we find the best overall consistency – namely the ClO/Cl2O2 equilibrium constant suggested by Plenge et al. (2005), the Cl2O2 recombination rate constant reported by Nickolaisen et al. (1994) and Cl2O2 photolysis rates based on absorption cross sections in the range between the JPL 2006 assessment and the laboratory study by Burkholder et al. (1990) – is not congruent with the latest recommendations given by the JPL and IUPAC panels and does not represent the laboratory studies currently regarded as the most reliable experimental values. We show that the incorporation of new Pope et al. (2007) Cl2O2 absorption cross sections into several models, combined with best estimates for other key parameters (based on either JPL and IUPAC evaluations or on our study), results in severe model underestimates of observed ClO and observed ozone loss rates. This finding suggests either the existence of an unknown process that drives the partitioning of ClO and Cl2O2, or else some unidentified problem with either the laboratory study or numerous measurements of atmospheric ClO. Our mechanistic understanding of the ClO/Cl2O2 system is grossly lacking, with severe implications for our ability to simulate both present and future polar ozone depletion.


2017 ◽  
Vol 675 ◽  
pp. 56-62 ◽  
Author(s):  
Juan Carlos Gómez Martín ◽  
Shane M. Daly ◽  
James S.A. Brooke ◽  
John M.C. Plane

2020 ◽  
Vol 22 (17) ◽  
pp. 9448-9459 ◽  
Author(s):  
Zara S. Mir ◽  
Thomas R. Lewis ◽  
Lavinia Onel ◽  
Mark A. Blitz ◽  
Paul W. Seakins ◽  
...  

The UV absorption cross-sections of the Criegee intermediate CH2OO, and kinetics of the CH2OO self-reaction and the reaction of CH2OO with I are reported as a function of pressure at 298 K.


2016 ◽  
Vol 130 ◽  
pp. 172-179 ◽  
Author(s):  
Dian E. Romonosky ◽  
Nujhat N. Ali ◽  
Mariyah N. Saiduddin ◽  
Michael Wu ◽  
Hyun Ji (Julie) Lee ◽  
...  

2014 ◽  
Vol 14 (5) ◽  
pp. 2497-2508 ◽  
Author(s):  
J.-F. Müller ◽  
J. Peeters ◽  
T. Stavrakou

Abstract. Photolysis is shown to be a major sink for isoprene-derived carbonyl nitrates, which constitute an important component of the total organic nitrate pool over vegetated areas. Empirical evidence from published laboratory studies on the absorption cross sections and photolysis rates of α-nitrooxy ketones suggests that the presence of the nitrate group (i) greatly enhances the absorption cross sections and (ii) facilitates dissociation to a point that the photolysis quantum yield is close to unity, with O–NO2 dissociation as a likely major channel. On this basis, we provide new recommendations for estimating the cross sections and photolysis rates of carbonyl nitrates. The newly estimated photo rates are validated using a chemical box model against measured temporal profiles of carbonyl nitrates in an isoprene oxidation experiment by Paulot et al. (2009). The comparisons for ethanal nitrate and for the sum of methacrolein- and methyl vinyl ketone nitrates strongly supports our assumptions of large cross-section enhancements and a near-unit quantum yield for these compounds. These findings have significant atmospheric implications: the photorates of key carbonyl nitrates from isoprene are estimated to be typically between ~ 3 and 20 times higher than their sink due to reaction with OH in relevant atmospheric conditions. Moreover, since the reaction is expected to release NO2, photolysis is especially effective in depleting the total organic nitrate pool.


1997 ◽  
Vol 272 (5-6) ◽  
pp. 383-390 ◽  
Author(s):  
Palle Pagsberg ◽  
Erling Bjergbakke ◽  
Emil Ratajczak ◽  
Alfred Sillesen

1997 ◽  
Vol 101 (5) ◽  
pp. 853-863 ◽  
Author(s):  
Matthew H. Harwood ◽  
James B. Burkholder ◽  
Martin Hunter ◽  
R. W. Fox ◽  
A. R. Ravishankara

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