New ultraviolet absorption cross-sections of BrO at atmospheric temperatures measured by time-windowing Fourier transform spectroscopy

被引:196
作者
Fleischmann, OC
Hartmann, M
Burrows, JP [1 ]
Orphal, J
机构
[1] Univ Bremen, Inst Remote Sensing, D-28334 Bremen, Germany
[2] Univ Paris 11, Photophys Mol Lab, F-91405 Orsay, France
关键词
BrO; atmospheric remote sensing; absorption cross-section;
D O I
10.1016/j.jphotochem.2004.03.026
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The UV absorption cross-section spectra of the atmospherically important radical BrO have been determined using the recently developed technique of time-windowing Fourier transform spectroscopy (TW-FTS). The absorption spectra of the A(2)Pi(3/2)-X(2)Pi(3/2) band system were recorded in the flash photolysis of a gaseous mixture of Br(2) and O(3). The bromine-photo sensitized decomposition of O(3) was observed at five different temperatures between 203 and 298 K. The absolute UV absorption cross-section was determined from the time-dependent observation of reactant and product absorptions and by a kinetic analysis of the BrO behavior. The integrated UV absorption cross-section of BrO was, within the accuracy of the measurements, constant over the temperature range studied, as expected from spectroscopic considerations. For the (7, 0) vibrational band at 29 540 cm(-1) (338.5 nm), the peak absorption cross-sections were determined to be 2.19+/-0.23 at 298 K, 2.23+/-0.23 at 273 K, 2.52+/-0.26 at 243 K, 2.75+/-0.29 at 223 K, and 3.03+/-0.31 at 203 K (all in units X 10(-17) cm(2) per molecule, at a spectral resolution of 3.8 cm(-1), with error intervals of 2sigma). Further, vibrational constants and the dissociation limit for the electronic state A(2)Pi(3/2) were derived. The A <-- X dissociation energy was determined to be D(0) = 35 240+/-160 cm(-1) or 421.6+/-1.9 kJ/mol. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:117 / 132
页数:16
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