Collaborative Innovation Center of Atmospheric Environment and Equipment Technology, Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, School of Environmental Science and Engineering, Nanjing University of Information Science & Technology, 219 Ningliu Road, Nanjing, 210044, China; State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing, 210023, China; Oak Ridge Institute for Science and Education (ORISE), Office of Research and Development, U.S. Environmental Protection Agency, 109 T.W. Alexander Drive, Research Triangle Park, NC, 27711, USA; National Risk Management Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency, 109 T.W. Alexander Drive, Research Triangle Park, NC, 27711, USA.
National Risk Management Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency, 109 T.W. Alexander Drive, Research Triangle Park, NC, 27711, USA.
Environ Pollut. 2019 Jan;244:38-46. doi: 10.1016/j.envpol.2018.09.125. Epub 2018 Oct 8.
Light-absorbing organic carbon (OC), also referred to as "brown carbon" (BrC), has been intensively investigated in atmospheres impacted by biomass burning. However, other BrC sources (e.g., secondary formation in the atmosphere) are rarely studied in ambient aerosols. In the current work, forty-five PM filter samples were collected in Research Triangle Park (RTP), NC, USA from June 1st to July 15th, 2013. The bulk carbonaceous components, including OC, elemental carbon (EC), water soluble OC (WSOC), and an array of organic molecular markers were measured; an ultraviolet/visible spectrometer was used to measure the light absorption of methanol extractable OC and WSOC. The average light absorption per OC and WSOC mass of PM samples in summer RTP are 0.36 ± 0.16 m gC and 0.29 ± 0.13 m gC, respectively, lower than the ambient aerosol samples impacted by biomass burning and/or fossil fuel combustion (0.7-1.6 m gC) from other places. Less than 1% of the aqueous extracts absorption is attributed to the light-absorbing chromophores (nitroaromatic compounds) identified in this work. To identify the major sources of BrC absorption in RTP in the summer, Positive Matrix Factorization (PMF) was applied to a dataset containing optical properties and chemical compositions of carbonaceous components in PM. The results suggest that the formation of biogenic secondary organic aerosol (SOA) containing organosulfates is an important BrC source, contributing up to half of the BrC absorption in RTP during the summertime.
吸光有机碳(OC),也称为“棕色碳”(BrC),在受生物质燃烧影响的大气中得到了广泛研究。然而,在环境气溶胶中,其他 BrC 源(例如,大气中的二次形成)很少被研究。在当前的工作中,在美国北卡罗来纳州三角研究园(RTP)从 2013 年 6 月 1 日至 7 月 15 日收集了 45 个 PM 滤膜样本。测量了包括 OC、元素碳(EC)、水溶性 OC(WSOC)和一系列有机分子标志物在内的大量碳质成分;使用紫外/可见分光光度计测量了甲醇可提取 OC 和 WSOC 的光吸收。夏季 RTP 中 PM 样品的 OC 和 WSOC 质量的平均吸光率分别为 0.36±0.16m gC 和 0.29±0.13m gC,低于其他地方受生物质燃烧和/或化石燃料燃烧影响的环境气溶胶样品(0.7-1.6m gC)。水提取物吸光度的不到 1%归因于本工作中鉴定的吸光生色团(硝基芳香化合物)。为了确定夏季 RTP 中 BrC 吸光的主要来源,应用正矩阵因子化(PMF)对包含 PM 中碳质成分光学性质和化学成分的数据集进行分析。结果表明,含有有机硫酸盐的生物源二次有机气溶胶(SOA)的形成是一个重要的 BrC 源,在夏季占 RTP 中 BrC 吸光的一半以上。