标题:Role of Water Molecule in the Gas-Phase Formation Process of Nitrated Polycyclic Aromatic Hydrocarbons in the Atmosphere: A Computational Study
作者:Zhang, Qingzhu; Gao, Rui; Xu, Fei; Zhou, Qin; Jiang, Guibin; Wang, Tao; Chen, Jianmin; Hu, Jingtian; Jiang, Wei; Wang, Wenxing
作者机构:[Zhang, Qingzhu; Gao, Rui; Xu, Fei; Zhou, Qin; Chen, Jianmin; Hu, Jingtian; Jiang, Wei; Wang, Wenxing] Shandong Univ, Environm Res Inst, Jinan 250100, 更多
通讯作者:Zhang, Q
通讯作者地址:[Zhang, QZ]Shandong Univ, Environm Res Inst, Jinan 250100, Peoples R China.
来源:ENVIRONMENTAL SCIENCE & TECHNOLOGY
出版年:2014
卷:48
期:9
页码:5051-5057
DOI:10.1021/es500453g
摘要:Nitro-PAHs are globally worrisome air pollutants because their high direct-acting mutagenicity and carcinogenicity. A mechanistic understanding of their formation is of crucial importance for successful prevention of their atmospheric pollution. Here, the formation of nitro-PAHs arising from the OH-initiated and NO3-initiated atmospheric reactions of PAHs was investigated by using quantum chemical calculations. It is widely assumed that OH or NO3 radicals attack on the C atoms of the aromatic rings in the PAH molecule, followed by the addition of NO2 to the OH-PAH or NO3-PAH adducts at the ortho position and the loss of water or nitric acid to form nitro-PAHs. However, calculations show that the direct loss of water from the OH-NO2-PAH adducts via the unimolecular decomposition is energetically unfavorable. This study reveals for the first time that water molecule plays an important catalytic effect on the loss of water from the OH-NO2-PAH adducts and promotes the formation of nitro-PAHs. In addition, the introduction of water unwraps new formation pathway through the addition of NO2 to the OH-PAH or NO3-PAH adduct at the para position. The individual and overall rate constants for the addition reactions of PAHs with OH and NO3 radicals were deduced by using the Rice-Ramsperger-Kassel-Marcus (RRKM) theory.
收录类别:EI;SCOPUS;SCIE
WOS核心被引频次:33
Scopus被引频次:34
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84899828764&doi=10.1021%2fes500453g&partnerID=40&md5=37dfddbd338cd5a37a9037a298482abb
TOP