Hydroxyl radical and ozone initiated photochemical reactions of 1,3-butadiene

被引:69
作者
Liu, XY [1 ]
Jeffries, HE [1 ]
Sexton, KG [1 ]
机构
[1] Univ N Carolina, Dept Environm Sci & Engn, Chapel Hill, NC 27599 USA
关键词
diene; photochemical reaction mechanism; atmospheric chemistry; computational chemistry; PFBHA;
D O I
10.1016/S1352-2310(99)00078-3
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
1,3-Butadiene, classified as hazardous in the 1990 Clean Air Act Amendments, is an important ambient air pollutant. Understanding its atmospheric transformation is useful for its own sake, and is also helpful for eliciting isoprene's fate in the atmosphere (isoprene dominates the biogenic emissions in US). In this paper, samples from both hydroxyl- and ozone-initiated photooxidation of 1,3-butadiene were analyzed by derivatization with O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine followed by separation and detection by gas chromatography/ion trap mass spectrometry to detect and identify carbonyl compounds. The following carbonyls were observed: formaldehyde, acrolein, glycolaldehyde, glycidaldehyde, 3-hydroxy-propanaldehyde, hydroxy acetone, and malonaldehyde, which can be classified into three categories: epoxy carbonyls, hydroxyl carbonyls, and di-carbonyls. Three non-carbonyls, furan, 1,3-buatdiene monoxide, and 1,3-butadiene diepoxide, were also found. To confirm their identities, both commercially available and synthesized standards were used. To investigate the mechanism of 1,3-butadiene, separate batch reactor experiments for acrolein and 1,3-butadiene monoxide were carried out. Time series samples for several products were also taken. When necessary, computational chemistry methods were also employed. Based on these results, various schemes for the reaction mechanism are proposed. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3005 / 3022
页数:18
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