首页> 外文期刊>Journal of Geophysical Research. Biogeosciences >INVESTIGATION OF OH ABSORPTION CROSS SECTIONS OF ROTATIONAL TRANSITIONS IN THE A(2)SIGMA(+), V'=0 [- X(2)PI, V''=0 BAND UNDER ATMOSPHERIC CONDITIONS - IMPLICATIONS FOR TROPOSPHERIC LONG-PATH ABSORPTION MEASUREMENTS
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INVESTIGATION OF OH ABSORPTION CROSS SECTIONS OF ROTATIONAL TRANSITIONS IN THE A(2)SIGMA(+), V'=0 [- X(2)PI, V''=0 BAND UNDER ATMOSPHERIC CONDITIONS - IMPLICATIONS FOR TROPOSPHERIC LONG-PATH ABSORPTION MEASUREMENTS

机译:大气条件下A(2)SIGMA(+),V'= 0 [-X(2)PI,V''= 0带上的OH跃迁横截面的OH-研究

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摘要

The accuracy of tropospheric hydroxyl radical measurements by long-path absorption spectroscopy is ultimately limited by the uncertainty Or the effective OH absorption cross sections. The latter were determined from calculated spectra for the and Q(1)(2), Q(1)(3), and P-1(1) rotational lines of the OH A(2) Sigma(+), (upsilon'=0) <-- X(2)II, (v''=0) transition at 308 nm. The calculations took into account Doppler broadening, measured data of the collisional broadening of OH by air molecules, and instrumental line broadening effects. The calculated spectra were compared with OH absorption spectra measured in a flow-reactor near room temperature at 1013 hPa. Excellent agreement between calculated and measured OH spectra was achieved using the collision-broadening parameters determined recently by Leonard (1990). The effective absorption cross sections at the line center (peak absorption cross sections) calculated for the Voigt line shape at 300 K and 1013 hPa are: sigma(eff)((
机译:通过长径吸收光谱法测量对流层羟基自由基的准确性最终受到不确定性或有效OH吸收截面的限制。后者是根据OH A(2)Sigma(+)的Q和(1)(2),Q(1)(3)和P-1(1)旋转线的计算光谱确定的(upsilon' = 0)<-X(2)II,(v''= 0)在308 nm处跃迁。该计算考虑了多普勒展宽,空气分子对OH的碰撞展宽的测量数据以及仪器的谱线展宽效果。将计算出的光谱与在室温下在1013 hPa的流动反应器中测得的OH吸收光谱进行比较。使用伦纳德(Leonard,1990)最近确定的碰撞扩展参数,可以使计算出的OH光谱与测量的OH光谱达到极好的一致性。为Voigt线形在300 K和1013 hPa下计算的线中心有效吸收截面(峰值吸收截面)为:sigma(eff)((

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