Atmospheric fate of two relevant unsaturated ketoethers: kinetics, products and mechanisms for the reaction of hydroxyl radicals with (E)-4-methoxy-3-buten-2-one and (1E)-1-methoxy-2-methyl-1-penten-3-one

被引:5
作者
Gibilisco, Rodrigo Gaston [1 ]
Barnes, Ian [1 ]
Bejan, Iustinian Gabriel [2 ,3 ]
Wiesen, Peter [1 ]
机构
[1] Berg Univ Wuppertal, Inst Atmospher & Environm Res, D-42097 Wuppertal, Germany
[2] Alexandru Ioan Cuza Univ, Fac Chem, Dept Chem, 11 Carol I, Iasi 700506, Romania
[3] Alexandru Ioan Cuza Univ, Integrated Ctr Environm Sci Studies North Easter, 11 Carol I, Iasi 700506, Romania
关键词
ORGANIC-COMPOUNDS; METHYL NITRITE; OH RADICALS; CHEMISTRY; IDENTIFICATION; OXIDATION; SERIES; YIELDS;
D O I
10.5194/acp-20-8939-2020
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The kinetics of the gas phase reactions of hydroxyl radicals with two unsaturated ketoethers (UKEs) at (298 +/- 3) K and 1 atm of synthetic air have been studied for the first time using the relative-rate technique in an environmental reaction chamber by in situ Fourier-transform infrared spectroscopy (FTIR). The rate coefficients obtained using propene and isobutene as reference compounds were (in units of 10(-10) cm(3) molecule(-1) s(-1)) as follows: k(TMBO) (OH + (E)-4-methoxy-3-buten-2-one) = (1.41 +/- 0.11) and k(MMPO) (OH + (1E)-1-methoxy-2-methyl-1-penten-3-one) = (3.34 +/- 0.43). In addition, quantification of the main oxidation products in the presence of NOx has been performed, and degradation mechanisms for these reactions were developed. Methyl formate, methyl glyoxal, peroxyacetyl nitrate (PAN) and peroxypropionyl nitrate (PPN) were identified as main reaction products and quantified for both reactions. The results of the present study provide new insights regarding the contribution of these multifunctional volatile organic compounds (VOCs) in the generation of secondary organic aerosols (SOAs) and long-lived nitrogen containing compounds in the atmosphere. Atmospheric lifetimes and implications are discussed in light of the obtained results.
引用
收藏
页码:8939 / 8951
页数:13
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