New differential Fabry-Perot radiometer for remote sensing measurements of column CO 2 , O 2 , H 2 O and other atmospheric trace gases

2008 ◽  
Author(s):  
W. S. Heaps ◽  
E. Georgieva ◽  
E. Wilson
Keyword(s):  
Remote Sensing ◽  
Trace Gases ◽  
Atmospheric Trace Gases ◽  
Fabry Perot

scholarly journals Remote sensing atmospheric trace gases with infrared imaging spectroscopy

Eos ◽  
2012 ◽  
Vol 93 (50) ◽  
pp. 525-525 ◽  
Author(s):  
Ira Leifer ◽  
David M. Tratt ◽  
Vincent J. Realmuto ◽  
Konstantin Gerilowski ◽  
John P. Burrows
Keyword(s):  
Remote Sensing ◽  
Infrared Imaging ◽  
Trace Gases ◽  
Imaging Spectroscopy ◽  
Atmospheric Trace Gases

Remote sensing ‘ground-based automatic UV / visible spectrometer’ for the study of atmospheric trace gases

2009 ◽  
Vol 30 (21) ◽  
pp. 5633-5653 ◽  
Author(s):  
G. S. Meena ◽  
A. L. Londhe ◽  
C. S. Bhosale ◽  
D. B. Jadhav
Keyword(s):  
Remote Sensing ◽  
Trace Gases ◽  
Atmospheric Trace Gases ◽  
Uv Visible

Towards Remote Sensing of Atmospheric Trace Gases in the UV spectral range using Dual-Comb spectroscopy

2021 ◽  
Author(s):  
Clément Pivard ◽  
Sandrine Galtier ◽  
Patrick Rairoux
Keyword(s):  
Remote Sensing ◽  
Spectral Range ◽  
Near Infrared ◽  
Frequency Comb ◽  
Trace Gases ◽  
In Situ Monitoring ◽  
Atmospheric Trace Gases ◽  
The Impact ◽  
Uv Range

<p>The development of increasingly sensitive and robust instruments and new methodologies are essential to improve our understanding of the Earth’s climate and air pollution. In this context, Dual-Comb spectroscopy (DCS) appears as an emerging spectroscopy methodology to detect in situ, without air-sampling, atmospheric trace-gases.</p><p>DCS is a Fourier-transform type experiment that takes advantage of mode-locked femtosecond (fs) pulses. This methodology appears highly relevant for atmosphere remote-sensing studies because of its very fast acquisition rate (>kHz) that reduces the impact of atmospheric turbulences on the retrieved spectra. DCS has been successfully applied in near-infrared (NIR) spectral ranges for atmospheric greenhouse gas monitoring (water vapor, carbon dioxide, and methane) [1-2].</p><p>Its implementation in the UV range would offer a new spectroscopic intrumentation to target the most reactive species of the atmosphere (OH, HONO, BrO...) as they have their greatest absorption cross-sections in the UV range. UV-DCS would therefore be an answer to the lack of variability of today operationnal and in situ monitoring instrument for those reactive molecules.</p><p>We will present a potential light source for remote sensing UV-DCS and discuss the degree of immunity of UV-DCS to atmospheric turbulences. We will show to which extent the characteristics of the currently available UV sources are compatible with the unambiguous identification of UV absorbing gases by UV-DCS. We will finally present the performances of UV-DCS in terms of concentration detection limit for several UV absorbing molecules (OH, BrO, NO<sub>2</sub>, OClO, HONO, CH<sub>2</sub>O, SO<sub>2</sub>). This sensitivity study has been recently published [3] and the main results will be presented.</p><p> </p><p>[1] Rieker, G.B.; Giorgetta, F.R.; Swann, W.C.; Kofler, J.; Zolot, A.M.; Sinclair, L.C.; Baumann, E.; Cromer, C.;Petron, G.; Sweeney, C.; et al. « Frequency-comb-based remote sensing of greenhouse gases over kilometer air Paths ». Optica 1, p. 290–298 (2014)</p><p>[2] Oudin, J.; Mohamed, A.K.; Hébert, P.J. "IPDA LIDAR measurements on atmospheric CO2 and H2O using dual comb spectroscopy," Proc. SPIE 11180, International Conference on Space Optics — ICSO 2018, p. 111802N (12 July 2019)</p><p>[3] Galtier, S.; Pivard, C.; Rairoux, P. Towards DCS in the UV Spectral Range for Remote Sensing of Atmospheric Trace Gases. Remote Sens., 12, p.3444 (2020)</p>

scholarly journals Towards imaging of atmospheric trace gases using Fabry Perot Interferometer Correlation Spectroscopy in the UV and visible spectral range

2018 ◽  
Author(s):  
Jonas Kuhn ◽  
Ulrich Platt ◽  
Nicole Bobrowski ◽  
Thomas Wagner
Keyword(s):  
Temporal Resolution ◽  
State Of The Art ◽  
Trace Gases ◽  
Visible Spectral Range ◽  
Correlation Spectroscopy ◽  
Trace Gas ◽  
Atmospheric Trace Gases ◽  
Fabry Perot ◽  
Sensitivity And Selectivity ◽  
Spatio Temporal

Abstract. Many processes in the lower atmosphere including transport, turbulent mixing and chemical conversions happen on time scales of the order of seconds (e.g. at point sources). Remote sensing of atmospheric trace gases in the UV and visible spectral range (UV/Vis) commonly uses dispersive spectroscopy (e.g. Differential Optical Absorption Spectroscopy, DOAS). The recorded spectra allow for the direct identification, separation and quantification of narrow band absorption of trace gases. However, these techniques are typically limited to a single viewing direction and limited by the light throughput of the spectrometer setup. While two dimensional imaging is possible by spatial scanning, the temporal resolution remains poor (often several minutes per image). Therefore, processes on time scales of seconds cannot be directly resolved by state of the art dispersive methods. We investigate the application of Fabry-Perot Interferometers (FPIs) for the optical remote sensing of atmospheric trace gases in the UV/Vis. By choosing a FPI transmission spectrum, which is optimised to correlate with narrow band (ideally periodic) absorption structures of the target trace gas, column densities of the trace gas can be determined with a sensitivity and selectivity comparable to dispersive spectroscopy, using only a small number of spectral channels (FPI tuning settings). Different from dispersive optical elements, the FPI can be implemented in full frame imaging setups (cameras), which can reach high spatio-temporal resolution. In principle, FPI Correlation Spectroscopy can be applied for any trace gas with distinct absorption structures in the UV/Vis. We present calculations for the application of FPI Correlation Spectroscopy to SO2, BrO and NO2 for exemplary measurement scenarios. Besides high sensitivity and selectivity we find that the spatio temporal resolution of FPI Correlation Spectroscopy can be more than two orders of magnitude higher than state of the art DOAS measurements. As proof of concept we built a one-pixel prototype implementing the technique for SO2 in the UV. Good agreement with our calculations and conventional measurement techniques are demonstrated and no cross sensitivities to other trace gases are observed.

scholarly journals Towards imaging of atmospheric trace gases using Fabry–Pérot interferometer correlation spectroscopy in the UV and visible spectral range

2019 ◽  
Vol 12 (1) ◽  
pp. 735-747 ◽  
Author(s):  
Jonas Kuhn ◽  
Ulrich Platt ◽  
Nicole Bobrowski ◽  
Thomas Wagner
Keyword(s):  
Temporal Resolution ◽  
Spectral Range ◽  
Trace Gases ◽  
Visible Spectral Range ◽  
Correlation Spectroscopy ◽  
Trace Gas ◽  
Atmospheric Trace Gases ◽  
Fabry Perot ◽  
Sensitivity And Selectivity ◽  
Spatio Temporal

Abstract. Many processes in the lower atmosphere including transport, turbulent mixing and chemical conversions happen on timescales of the order of seconds (e.g. at point sources). Remote sensing of atmospheric trace gases in the UV and visible spectral range (UV–Vis) commonly uses dispersive spectroscopy (e.g. differential optical absorption spectroscopy, DOAS). The recorded spectra allow for the direct identification, separation and quantification of narrow-band absorption of trace gases. However, these techniques are typically limited to a single viewing direction and limited by the light throughput of the spectrometer set-up. While two-dimensional imaging is possible by spatial scanning, the temporal resolution remains poor (often several minutes per image). Therefore, processes on timescales of seconds cannot be directly resolved by state-of-the-art dispersive methods. We investigate the application of Fabry–Pérot interferometers (FPIs) for the optical remote sensing of atmospheric trace gases in the UV–Vis spectral range. By choosing a FPI transmission spectrum, which is optimised to correlate with narrow-band (ideally periodic) absorption structures of the target trace gas, column densities of the trace gas can be determined with a sensitivity and selectivity comparable to dispersive spectroscopy, using only a small number of spectral channels (FPI tuning settings). Different from dispersive optical elements, the FPI can be implemented in full-frame imaging set-ups (cameras), which can reach high spatio-temporal resolution. In principle, FPI correlation spectroscopy can be applied for any trace gas with distinct absorption structures in the UV–Vis range. We present calculations for the application of FPI correlation spectroscopy to SO2, BrO and NO2 for exemplary measurement scenarios. In addition to high sensitivity and selectivity we find that the spatio temporal resolution of FPI correlation spectroscopy can be more than 2 orders of magnitude higher than state-of-the-art DOAS measurements. As proof of concept we built a 1-pixel prototype implementing the technique for SO2 in the UV. Good agreement with our calculations and conventional measurement techniques is demonstrated and no cross sensitivities to other trace gases are observed.

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