Published June 28, 2006 | Version v1
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HDO and D2O long path spectroscopy: Ongoing work of the Brussels-Reims Team

  • 1. Université de Reims, GSMA, BP 1039, 51687 Reims Cedex 2, FRANCE. (http://helios.univ-reims.fr/Labos/)
  • 2. Université Libre de Bruxelles, Service de Chimie Quantique et Photophysique, C.P. 160/09, 50 Avenue F.D. Roosevelt, B-1050 Brussels, BELGIUM. (http://www.ulb.ac.be/cpm)
  • 3. Institut d'Aéronomie Spatiale de Belgique, 3 Av Circulaire, B-1180 Brussels, BELGIUM. (http://www.aeronomie.be)

Description

Laboratory absorption spectra of H2O-D2O mixtures have been recorded in the spectral region 8800-1500 cm-1 by Fourier transform spectroscopy at high resolution (0.03 cm-1 ). The 50 m base long cell from Reims was used to record spectra with total pressure £ absorption path products of about 6000 torr m. In the continuation of our previous work concerning water vapor 1 ; 2 ; 3 ; 4 ; 5 ; 6 ; 7 ; 8 ; 9 ; 10 , the present study deals with the Deuterium enriched spectra. Two spectra with diÆerent mixing ratios for H 2 O, HDO and D 2 O species were recorded. The identiØcation of the HDO and D 2 O lines has been made by comparison of ratios between pure and enriched spectra. Partial pressures were carefully determined using (i) H2 ^16O previously determined line intensities, (ii) HDO and D 2 O line intensity ratios, and (iii) total pressures. The lines identiØcation was checked through the evolution of the integrated absorption coe±cients with the partial pressures. The observed lines have been Øtted to Voigt line proØles from which line positions (cali- brated afterwards), integrated absorption cross-sections and self-broadening coe±cients have been determined. For the two deuterated species the integrated absorption cross sections could be measured down to 5 10-27 cm/molecule. Comparisons with the most recent experimental data and calculations are presented.

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References

  • M. Carleeret al., J. Chem. Phys. 111(6), 2444-2450 (1999).
  • M. Carleeret al., J. Chem. Phys. 111(6), 2444-2450 (1999).
  • M. Carleeret al., J. Chem. Phys. 111(6), 2444-2450 (1999).
  • M. Carleeret al., J. Chem. Phys. 111(6), 2444-2450 (1999).
  • M. Carleeret al., J. Chem. Phys. 111(6), 2444-2450 (1999).
  • M. Carleeret al., J. Chem. Phys. 111(6), 2444-2450 (1999).
  • M. Carleeret al., J. Chem. Phys. 111(6), 2444-2450 (1999).
  • M. Carleeret al., J. Chem. Phys. 111(6), 2444-2450 (1999).
  • M. Carleeret al., J. Chem. Phys. 111(6), 2444-2450 (1999).
  • M. Carleeret al., J. Chem. Phys. 111(6), 2444-2450 (1999).