An intercomparison of CH<sub>3</sub>O<sub>2</sub> measurements by fluorescence assay by gas expansion and cavity ring-down spectroscopy within HIRAC (Highly Instrumented Reactor for Atmospheric Chemistry)
Abstrak
<p>Simultaneous measurements of <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span> radical concentrations have been performed using two different methods in the Leeds HIRAC (Highly Instrumented Reactor for Atmospheric Chemistry) chamber at 295 K and in 80 mbar of a mixture of <span class="inline-formula">3:1</span> <span class="inline-formula">He∕O<sub>2</sub></span> and 100 or 1000 mbar of synthetic air. The first detection method consisted of the indirect detection of <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span> using the conversion of <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span> into <span class="inline-formula">CH<sub>3</sub>O</span> by excess NO with subsequent detection of <span class="inline-formula">CH<sub>3</sub>O</span> by fluorescence assay by gas expansion (FAGE). The FAGE instrument was calibrated for <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span> in two ways. In the first method, a known concentration of <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span> was generated using the 185 nm photolysis of water vapour in synthetic air at atmospheric pressure followed by the conversion of the generated OH radicals to <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span> by reaction with <span class="inline-formula">CH<sub>4</sub>∕O<sub>2</sub></span>. This calibration can be used for experiments performed in HIRAC at 1000 mbar in air. In the second method, calibration was achieved by generating a near steady state of <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span> and then switching off the photolysis lamps within HIRAC and monitoring the subsequent decay of <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span>, which was controlled via its self-reaction, and analysing the decay using second-order kinetics. This calibration could be used for experiments performed at all pressures. In the second detection method, <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span> was measured directly using cavity ring-down spectroscopy (CRDS) using the absorption at 7487.98 cm<span class="inline-formula"><sup>−1</sup></span> in the <span class="inline-formula"><i>A</i>←<i>X</i></span> (<span class="inline-formula"><i>ν</i><sub>12</sub></span>) band with the optical path along the <span class="inline-formula">∼1.4</span> m chamber diameter. Analysis of the second-order kinetic decays of <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span> by self-reaction monitored by CRDS has been used for the determination of the <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span> absorption cross section at 7487.98 cm<span class="inline-formula"><sup>−1</sup></span>, both at 100 mbar of air and at 80 mbar of a <span class="inline-formula">3:1</span> <span class="inline-formula">He∕O<sub>2</sub></span> mixture, from which <span class="inline-formula"><math xmlns="http://www.w3.org/1998/Math/MathML" id="M26" display="inline" overflow="scroll" dspmath="mathml"><mrow><msub><mi mathvariant="italic">σ</mi><mrow class="chem"><msub><mi mathvariant="normal">CH</mi><mn mathvariant="normal">3</mn></msub><msub><mi mathvariant="normal">O</mi><mn mathvariant="normal">2</mn></msub></mrow></msub><mo>=</mo><mo>(</mo><mn mathvariant="normal">1.49</mn><mo>±</mo><mn mathvariant="normal">0.19</mn><mo>)</mo><mo>×</mo><msup><mn mathvariant="normal">10</mn><mrow><mo>-</mo><mn mathvariant="normal">20</mn></mrow></msup></mrow></math><span><svg:svg xmlns:svg="http://www.w3.org/2000/svg" width="146pt" height="18pt" class="svg-formula" dspmath="mathimg" md5hash="a0de3b239060922dec1332333490d350"><svg:image xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="amt-13-2441-2020-ie00001.svg" width="146pt" height="18pt" src="amt-13-2441-2020-ie00001.png"/></svg:svg></span></span> cm<span class="inline-formula"><sup>2</sup></span> molecule<span class="inline-formula"><sup>−1</sup></span> was determined for both pressures. The absorption spectrum of <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span> between 7486 and 7491 cm<span class="inline-formula"><sup>−1</sup></span> did not change shape when the total pressure was increased to 1000 mbar, from which we determined that <span class="inline-formula"><math xmlns="http://www.w3.org/1998/Math/MathML" id="M31" display="inline" overflow="scroll" dspmath="mathml"><mrow><msub><mi mathvariant="italic">σ</mi><mrow class="chem"><msub><mi mathvariant="normal">CH</mi><mn mathvariant="normal">3</mn></msub><msub><mi mathvariant="normal">O</mi><mn mathvariant="normal">2</mn></msub></mrow></msub></mrow></math><span><svg:svg xmlns:svg="http://www.w3.org/2000/svg" width="34pt" height="12pt" class="svg-formula" dspmath="mathimg" md5hash="91f987b38bd7263d5c8018a9bd5e863c"><svg:image xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="amt-13-2441-2020-ie00002.svg" width="34pt" height="12pt" src="amt-13-2441-2020-ie00002.png"/></svg:svg></span></span> is independent of pressure over the pressure range 100–1000 mbar in air. <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span> was generated in HIRAC using either the photolysis of <span class="inline-formula">Cl<sub>2</sub></span> with UV black lamps in the presence of <span class="inline-formula">CH<sub>4</sub></span> and <span class="inline-formula">O<sub>2</sub></span> or the photolysis of acetone at 254 nm in the presence of <span class="inline-formula">O<sub>2</sub></span>. At 1000 mbar of synthetic air the correlation plot of [<span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span>]<span class="inline-formula"><sub>FAGE</sub></span> against [<span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span>]<span class="inline-formula"><sub>CRDS</sub></span> gave a gradient of <span class="inline-formula">1.09±0.06</span>. At 100 mbar of synthetic air the FAGE–CRDS correlation plot had a gradient of <span class="inline-formula">0.95±0.024</span>, and at 80 mbar of <span class="inline-formula">3:1</span> <span class="inline-formula">He∕O<sub>2</sub></span> mixture the correlation plot gradient was <span class="inline-formula">1.03±0.05</span>. These results provide a validation of the FAGE method to determine concentrations of <span class="inline-formula">CH<sub>3</sub>O<sub>2</sub></span>.</p>
Topik & Kata Kunci
Penulis (11)
L. Onel
A. Brennan
M. Gianella
J. Hooper
N. Ng
G. Hancock
L. Whalley
L. Whalley
P. W. Seakins
G. A. D. Ritchie
D. E. Heard
Format Sitasi
Akses Cepat
- Tahun Terbit
- 2020
- Sumber Database
- DOAJ
- DOI
- 10.5194/amt-13-2441-2020
- Akses
- Open Access ✓