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  Using total OH reactivity to assess isoprene photooxidation via measurement and model

Nölscher, A. C., Butler, T., Auld, J., Veres, P., Muñoz, A., Taraborrelli, D., Vereecken, L., Lelieveld, J., & Williams, J. (2014). Using total OH reactivity to assess isoprene photooxidation via measurement and model. Atmospheric Environment, 89, 453-463. doi:10.1016/j.atmosenv.2014.02.024.

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資料種別: 学術論文

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Nölscher, A. C.1, 著者           
Butler, T.2, 著者
Auld, J.1, 著者           
Veres, P.1, 著者           
Muñoz, A.2, 著者
Taraborrelli, D.1, 著者           
Vereecken, L.1, 著者           
Lelieveld, J.1, 著者           
Williams, J.1, 著者           
所属:
1Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826285              
2external, ou_persistent22              

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 要旨: The Tropics provide a reactive atmospheric environment with high levels of biogenic emissions, rapidly growing anthropogenic influence, high solar radiation and temperature levels. The major reactive biogenic emission is isoprene which reacts rapidly with the primary daytime oxidant OH, the hydroxyl radical. This key photooxidation process has recently been the focus of several experimental and computational studies. A novel isoprene degradation mechanism was recently proposed (MIME) supplementing the commonly used MCM 3.2 scheme. This study examined the photooxidation of isoprene in the controlled conditions of the Valencia atmospheric reaction chamber, EUPHORE (EUropean PHOtoREactor). Besides the detection of isoprene and its major oxidation products formaldehyde, methyl vinyl ketone (MVK) and methacrolein (MACR), the total loss rate of OH (total OH reactivity) was measured. The total OH reactivity was compared to the individual measurements of isoprene and its oxidation products to assess the significant contributors to the overall OH loss rate. Measured total OH reactivity showed excellent agreement to the calculation based on individual compounds detected by a Proton-Transfer-Reaction-Time-Of-Flight-Mass-Spectrometer (PTR-TOF-MS). On average 97% of the measured total OH reactivity could be explained by isoprene and its major oxidation products. Total OH reactivity was also compared to various isoprene degradation schemes to evaluate known mechanisms. The MCM 3.2 isoprene mechanism reproduced the temporal degradation of total OH reactivity (and isoprene) reasonably well with a 57% (and 95%) agreement within the model uncertainties and a linear curve fit slope of 0.69 (and 1.02) for a model to measurement correlation. Large discrepancies between modeled values and all observed compounds were found for the recent isoprene oxidation scheme in MIME. Possible mechanistic reasons are discussed and improvements proposed. The subsequently modified version of MIME differed from the measured total OH reactivity only about 12% at the end of the experiment and represented best the overall temporal profile (linear curve fit slope of correlation: 0.95). (C) 2014 Elsevier Ltd. All rights reserved.

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 日付: 2014-06
 出版の状態: 出版
 ページ: -
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 識別子(DOI, ISBNなど): ISI: 000335874500049
DOI: 10.1016/j.atmosenv.2014.02.024
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出版物 1

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出版物名: Atmospheric Environment
種別: 学術雑誌
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出版社, 出版地: Oxford [England] : Pergamon
ページ: - 巻号: 89 通巻号: - 開始・終了ページ: 453 - 463 識別子(ISBN, ISSN, DOIなど): ISSN: 1352-2310
CoNE: https://pure.mpg.de/cone/journals/resource/958480288336