Pressure Broadening of H2O Absorption Lines in the 1.3 μm Region Measured by Continuous Wave-Cavity Ring-Down Spectroscopy: Application in the Trace Detection of Water Vapor in N2, SiH4, CF4, and PH3

2008 ◽  
Vol 62 (12) ◽  
pp. 1354-1362 ◽  
Author(s):  
Phyllis A. Y. Fiadzomor ◽  
Derek M. Baker ◽  
Anthony M. Keen ◽  
Robert B. Grant ◽  
Andrew J. Orr-Ewing
2007 ◽  
Vol 90 (1) ◽  
pp. 1-9 ◽  
Author(s):  
M. Pradhan ◽  
R.E. Lindley ◽  
R. Grilli ◽  
I.R. White ◽  
D. Martin ◽  
...  

2010 ◽  
Vol 3 (2) ◽  
pp. 375-386 ◽  
Author(s):  
H. Chen ◽  
J. Winderlich ◽  
C. Gerbig ◽  
A. Hoefer ◽  
C. W. Rella ◽  
...  

Abstract. High-accuracy continuous measurements of greenhouse gases (CO2 and CH4) during the BARCA (Balanço Atmosférico Regional de Carbono na Amazônia) phase B campaign in Brazil in May 2009 were accomplished using a newly available analyzer based on the cavity ring-down spectroscopy (CRDS) technique. This analyzer was flown without a drying system or any in-flight calibration gases. Water vapor corrections associated with dilution and pressure-broadening effects for CO2 and CH4 were derived from laboratory experiments employing measurements of water vapor by the CRDS analyzer. Before the campaign, the stability of the analyzer was assessed by laboratory tests under simulated flight conditions. During the campaign, a comparison of CO2 measurements between the CRDS analyzer and a nondispersive infrared (NDIR) analyzer on board the same aircraft showed a mean difference of 0.22±0.09 ppm for all flights over the Amazon rain forest. At the end of the campaign, CO2 concentrations of the synthetic calibration gases used by the NDIR analyzer were determined by the CRDS analyzer. After correcting for the isotope and the pressure-broadening effects that resulted from changes of the composition of synthetic vs. ambient air, and applying those concentrations as calibrated values of the calibration gases to reprocess the CO2 measurements made by the NDIR, the mean difference between the CRDS and the NDIR during BARCA was reduced to 0.05±0.09 ppm, with the mean standard deviation of 0.23±0.05 ppm. The results clearly show that the CRDS is sufficiently stable to be used in flight without drying the air or calibrating in flight and the water corrections are fully adequate for high-accuracy continuous airborne measurements of CO2 and CH4.


2009 ◽  
Vol 97 (2) ◽  
pp. 523-528 ◽  
Author(s):  
D. Yamano ◽  
Y. Sakamoto ◽  
A. Yabushita ◽  
M. Kawasaki ◽  
I. Morino ◽  
...  

2006 ◽  
Vol 8 (3) ◽  
pp. 364-368 ◽  
Author(s):  
Shinji Nakamichi ◽  
Yoshimitsu Kawaguchi ◽  
Hisato Fukuda ◽  
Shinichi Enami ◽  
Satoshi Hashimoto ◽  
...  

2002 ◽  
Vol 4 (24) ◽  
pp. 5960-5965 ◽  
Author(s):  
B. L. Fawcett ◽  
A. M. Parkes ◽  
D. E. Shallcross ◽  
A. J. Orr-Ewing

2007 ◽  
Vol 334 (1-3) ◽  
pp. 196-203 ◽  
Author(s):  
Tomoki Nakayama ◽  
Hisato Fukuda ◽  
Akihiro Sugita ◽  
Satoshi Hashimoto ◽  
Masahiro Kawasaki ◽  
...  

2009 ◽  
Vol 38 (10) ◽  
pp. 1000-1001 ◽  
Author(s):  
Yosuke Sakamoto ◽  
Daisuke Yamano ◽  
Tomoki Nakayama ◽  
Masahiro Kawasaki ◽  
Isamu Morino ◽  
...  

2012 ◽  
Vol 5 (11) ◽  
pp. 2689-2701 ◽  
Author(s):  
H. Nara ◽  
H. Tanimoto ◽  
Y. Tohjima ◽  
H. Mukai ◽  
Y. Nojiri ◽  
...  

Abstract. We examined potential interferences from water vapor and atmospheric background gases (N2, O2, and Ar), and biases by isotopologues of target species, on accurate measurement of atmospheric CO2 and CH4 by means of wavelength-scanned cavity ring-down spectroscopy (WS-CRDS). Changes of the background gas mole fractions in the sample air substantially impacted the CO2 and CH4 measurements: variation of CO2 and CH4 due to relative increase of each background gas increased as Ar < O2 < N2, suggesting similar relation for the pressure-broadening effects (PBEs) among the background gas. The pressure-broadening coefficients due to variations in O2 and Ar for CO2 and CH4 are empirically determined from these experimental results. Calculated PBEs using the pressure-broadening coefficients are linearly correlated with the differences between the mole fractions of O2 and Ar and their ambient abundances. Although the PBEs calculation showed that impact of natural variation of O2 is negligible on the CO2 and CH4 measurements, significant bias was inferred for the measurement of synthetic standard gases. For gas standards balanced with purified air, the PBEs were estimated to be marginal (up to 0.05 ppm for CO2 and 0.01 ppb for CH4) although the PBEs were substantial (up to 0.87 ppm for CO2 and 1.4 ppb for CH4) for standards balanced with synthetic air. For isotopic biases on CO2 measurements, we compared experimental results and theoretical calculations, which showed excellent agreement within their uncertainty. We derived instrument-specific water correction functions empirically for three WS-CRDS instruments (Picarro EnviroSense 3000i, G-1301, and G-2301), and evaluated the transferability of the water correction function from G-1301 among these instruments. Although the transferability was not proven, no significant difference was found in the water vapor correction function for the investigated WS-CRDS instruments as well as the instruments reported in the past studies within the typical analytical precision at sufficiently low water concentrations (<0.7% for CO2 and <0.6% for CH4). For accurate measurements of CO2 and CH4 in ambient air, we concluded that WS-CRDS measurements should be performed under complete dehumidification of air samples, or moderate dehumidification followed by application of a water vapor correction function, along with calibration by natural air-based standard gases or purified air-balanced synthetic standard gases with the isotopic correction.


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