Measurements of Ozone, Nitrogen Dioxide and Sulfur Dioxide by an Open-Path Differential Optical Absorption Spectrometer in Higashi-Hiroshima, Hiroshima Prefecture

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  • 広島県東広島市におけるオープンパス差分光吸収分光法によるオゾン,二酸化窒素,二酸化硫黄の測定
  • ヒロシマケン ヒガシヒロシマシ ニ オケル オープンパス サブン ヒカリキュウシュウ ブンコウホウ ニ ヨル オゾン 2サンカ チッソ 2サンカ イオウ ノ ソクテイ

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A field-based intercomparison study of a commercial open-path differential optical absorption spectrometer (DOAS) and conventional point monitoring techniques for ozone (O3), nitrogen dioxide (NO2) and sulfur dioxide (SO2) was conducted from August to September, 1999, in Higashi-Hiroshima, Hiroshima prefecture. O3, NO2 and SO2 were measured every 10 minutes by an ultraviolet-ray absorption method, a chemiluminescence method, and a fluorescence method, respectively, while all of these three gases were simultaneously monitored every 20 minutes by the DOAS system (DOAS 2000, Thermo Electron Nippon Co. Ltd., Japan). Very good correlations were found for O3 (r2 = 0.96) and SO2 (r2 = 0.93), while a slightly lower correlation existed for NO2 (r2 = 0.80). The average concentrations of these gases monitored by the DOAS system were 1.1, 1.2, 1.6 times higher than those measured by conventional point monitors, respectively. Vehicle emissions from the surrounding area of the monitoring site caused atmospheric inhomogeneities, which were involved in the lower correlation for NO2 by causing differences in the analytical values of the two methods. A much higher slope of SO2 (1.6) was considered to result from the use of an inaccurate standard spectrum in DOAS analysis, which was prepared from 100 ppm level reference gas. Precipitation (0.5 ~ 35.0 mm h−1) and the relative humidity (25.6 ~ 99.9%) didn’t affect the DOAS measurements. Fog interrupted the DOAS measurements of all compounds in during several periods; it occurred when the relative humidity was kept over 99% for a few hours from midnight to morning. The mobile emitting source and the meteorological situations should be considered when monitoring is carried out by DOAS.<br>

Journal

  • BUNSEKI KAGAKU

    BUNSEKI KAGAKU 54 (4), 325-329, 2005

    The Japan Society for Analytical Chemistry

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