pulsed photolysis
Recently Published Documents


TOTAL DOCUMENTS

24
(FIVE YEARS 3)

H-INDEX

7
(FIVE YEARS 0)

2020 ◽  
Vol 14 (3) ◽  
pp. 488-491
Author(s):  
G. R. Kalamkarov ◽  
T. F. Shevchenko ◽  
P. V. Aboltin ◽  
T. S. Konstantinova ◽  
P. P. Levin

2019 ◽  
Vol 93 (7) ◽  
pp. 1417-1419
Author(s):  
V. I. Porkhun ◽  
A. V. Arshinov ◽  
G. Yu. Vasil’eva ◽  
V. E. Avvakumov

2007 ◽  
Vol 7 (6) ◽  
pp. 1565-1574 ◽  
Author(s):  
E. Jiménez ◽  
B. Lanza ◽  
E. Martínez ◽  
J. Albaladejo

Abstract. The ultraviolet (λ=250–370 nm) photolysis and the OH-initiated oxidation of hexanal and trans-2-hexenal, which are relevant atmospheric processes, have been investigated at room temperature and as a function of temperature (T=263–353 K), respectively. This kinetic study as a function of temperature is reported here for the first time. Absolute absorption cross sections (σλ) were obtained using a recently built system operating in the UV region. The obtained σλ allowed the estimation of the photolysis rates (J) across the troposphere. Kinetic measurements of the gas-phase reaction of hydroxyl radicals (OH) with hexanal and trans-2-hexenal were performed by using the laser pulsed photolysis/laser-induced fluorescence technique. Rate coefficients kOH for both aldehydes were determined at temperatures between 263 and 353 K at 50 Torr in helium or argon bath gases. The temperature dependence of kOH for both aldehydes was found to be slightly negative. The tropospheric lifetime of hexanal and trans-2-hexenal due to the chemical removal by OH radicals has been estimated across the troposphere. The loss rate due to the OH chemical removal was compared with the estimated photolysis rates. Our results show that OH-reaction is the main loss process for these aldehydes in the troposphere, although photolysis is not negligible for hexanal.


2006 ◽  
Vol 6 (6) ◽  
pp. 13225-13250 ◽  
Author(s):  
E. Jiménez ◽  
B. Lanza ◽  
E. Martínez ◽  
J. Albaladejo

Abstract. The ultraviolet (λ=250–370 nm) photolysis and the OH-initiated oxidation of hexanal and trans-2-hexenal, which are relevant atmospheric processes, have been investigated at room temperature and as a function of temperature (T=263–353 K), respectively. This kinetic study as a function of temperature is reported here for the first time. Absolute absorption cross sections (σλ) were obtained using a recently built system operating in the UV region. This work represents the first reported σλ for trans-2-hexenal. The obtained σλ allowed the estimation of the photolysis rates (J) of hexanal and trans-2-hexenal across the troposphere. Kinetic measurements of the gas-phase reaction of hydroxyl radicals (OH) with hexanal and trans-2-hexenal were performed by using the laser pulsed photolysis/laser-induced fluorescence technique. Rate coefficients kOH for both aldehydes were determined at temperatures between 263 and 353 K at 50 Torr in helium or argon bath gases. The temperature dependence of kOH for both aldehydes was found to be slightly negative. The tropospheric lifetime of hexanal and trans-2-hexenal due to the chemical removal by OH radicals has been estimated across the troposphere. The loss rate due to the OH chemical removal was compared with the estimated photolysis rates. Our results show that OH-reaction and UV photolysis are the main loss processes for these aldehydes in the troposphere. For hexanal, both processes compete across the troposphere, however, UV photolysis can contribute up to 70% to the overall loss of trans-2-hexenal.


2000 ◽  
Vol 104 (2) ◽  
pp. 308-319 ◽  
Author(s):  
Scott L. Nickolaisen ◽  
Coleen M. Roehl ◽  
Lisa K. Blakeley ◽  
Randall R. Friedl ◽  
Joseph S. Francisco ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document