Homogeneous and heterogeneous reactions of anthracene with selected atmospheric oxidants |
| |
Authors: | Yang Zhang Jinian Shu Yuanxun Zhang Bo Yang |
| |
Affiliation: | 1. Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China;University of Chinese Academy of Sciences, Beijing 100049, China 2. Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China 3. University of Chinese Academy of Sciences, Beijing 100049, China |
| |
Abstract: | The reactions of gas-phase anthracene and suspended anthracene particles with O3 and O3-NO were conducted in a 200-L reaction chamber, respectively. The secondary organic aerosol (SOA) formations from gas-phase reactions of anthracene with O3 and O3-NO were observed. Meanwhile, the size distributions and mass concentrations of SOA were monitored with a scanning mobility particle sizer (SMPS) during the formation processes. The rapid exponential growths of SOA reveal that the atmospheric lifetimes of gas-phase anthracene towards O3 and O3-NO are less than 20.5 and 4.34 hr, respectively. The particulate oxidation products from homogeneous and heterogeneous reactions were analyzed with a vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer (VUV-ATOFMS). Gas chromatograph/mass spectrometer (GC/MS) analyses of oxidation products of anthracene were carried out for assigning the time-of-flight (TOF) mass spectra of products from homogeneous and heterogeneous reactions. Anthrone, anthraquinone, 9,10-dihydroxyanthracene, and 1,9,10-trihydroxyanthracene were the ozonation products of anthracene, while anthrone, anthraquinone, 9-nitroanthracene, and 1,8-dihydroxyanthraquinone were the main products of anthracene with O3-NO. |
| |
Keywords: | anthracene ozonation secondary organic aerosol heterogeneous reaction aerosol mass spectrometer |
本文献已被 CNKI 维普 万方数据 ScienceDirect 等数据库收录! |
| 点击此处可从《环境科学学报(英文版)》浏览原始摘要信息 |
|
点击此处可从《环境科学学报(英文版)》下载全文 |
|