Identification of products formed during the heterogeneous nitration and ozonation of polycyclic aromatic hydrocarbons

被引:40
|
作者
Cochran, Richard E. [1 ,2 ]
Jeong, Haewoo [1 ,3 ]
Haddadi, Shokouh [1 ,4 ]
Derseh, Rebeka Fisseha [1 ]
Gowan, Alexandra [1 ]
Beranek, Josef [1 ,5 ]
Kubatova, Alena [1 ]
机构
[1] Univ N Dakota, Dept Chem, 151 Cornell St,Stop 9024, Grand Forks, ND 58202 USA
[2] Univ Iowa, Dept Chem, E331 Chem Bldg, Iowa City, IA 52242 USA
[3] ACT Co Ltd, Mat Res Inst, Digital Empire 2,88 Sinwon Ro, Suwon, Gyeonggi Do, South Korea
[4] SUNY Coll Oswego, Dept Chem, Oswego, NY 13126 USA
[5] Zentiva Ks, Kabelovny 130, Prague, Czech Republic
基金
美国国家科学基金会;
关键词
Heterogeneous PAH oxidation; Product identification; Flow reactor; High resolution mass spectrometry; GAS-PHASE REACTIONS; PARTICULATE MATTER; PYRENE; PAHS; PARTICLES; OZONE; REACTIVITY; NO2; 2-NITROFLUORANTHENE; 1-NITROPYRENE;
D O I
10.1016/j.atmosenv.2015.12.036
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The 3- and 4-ring polycyclic aromatic hydrocarbons (PAHs) are the most abundant of PAHs in air particulate matter (PM). Thus we have investigated heterogeneous oxidation of 3- and 4-ring PAHs in a small-scale flow reactor using quartz filter as a support. Four representative PAHs, anthracene, phenanthrene, pyrene, and fluoranthene, were exposed to either NO2, O-3 or NO2+O-3 (NO3/N2O5) with a goal to identify and attempt quantification of major product distribution. A combination of gas chromatography with mass spectrometry (GC MS) with/without derivatization and liquid chromatography with high resolution MS (LC-HRMS) was used for identification. For the first time, a comprehensive characterization of a broad range of products enabled identifying ketone/diketone, aldehyde, hydroxyl, and carboxylic acid PAH derivatives. Exposure to NO3/N2O5 (formed by reacting NO2 with O-3, a more powerful reactant than either O-3 or NO2) produced additional compounds not observed with either oxidant alone. Multiple isomers of nitrofluoranthene and, for the first time, nitrophenanthrene were identified. In addition hydroxy-nitro-PAH derivatives were observed for the reaction of anthracene with NO3/N2O5. Monitoring of specific common ions such as those of 176 and 205 m/z attributed to carbonyl phenanthrene and deprotonated phenanthrene ions respectively was shown to be a useful tool for identification of multiple pyrene oxidation products. (C) 2015 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:92 / 103
页数:12
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