Docherty Kenneth S, Stone Elizabeth A, Ulbrich Ingrid M, DeCarlo Peter F, Snyder David C, Schauer James J, Peltier Richard E, Weber Rodney J, Murphy Shane M, Seinfeld John H, Grover Brett D, Eatough Delbert J, Jimenez Jose L
Cooperative Institute for Research in Environmental Sciences, University of Colorado, Boulder, Colorado, USA.
Environ Sci Technol. 2008 Oct 15;42(20):7655-62. doi: 10.1021/es8008166.
Ambient sampling was conducted in Riverside, California during the 2005 Study of Organic Aerosols in Riverside to characterize the composition and sources of organic aerosol using a variety of state-of-the-art instrumentation and source apportionmenttechniques. The secondary organic aerosol (SOA) mass is estimated by elemental carbon and carbon monoxide tracer methods, water soluble organic carbon content, chemical mass balance of organic molecular markers, and positive matrix factorization of high-resolution aerosol mass spectrometer data. Estimates obtained from each ofthese methods indicate that the organic fraction in ambient aerosol is overwhelmingly secondary in nature during a period of several weeks with moderate ozone concentrations and that SOA is the single largest component of PM1 aerosol in Riverside. Average SOA/OA contributions of 70-90% were observed during midday periods, whereas minimum SOA contributions of approximately 45% were observed during peak morning traffic periods. These results are contraryto previous estimates of SOAthroughout the Los Angeles Basin which reported that, other than during severe photochemical smog episodes, SOA was lower than primary OA. Possible reasons for these differences are discussed.
2005年在加利福尼亚州里弗赛德进行了环境采样,这是里弗赛德有机气溶胶研究的一部分,旨在使用各种最先进的仪器和源解析技术来表征有机气溶胶的组成和来源。通过元素碳和一氧化碳示踪法、水溶性有机碳含量、有机分子标志物的化学质量平衡以及高分辨率气溶胶质谱仪数据的正矩阵因子分解来估算二次有机气溶胶(SOA)的质量。从这些方法中的每一种获得的估算结果表明,在臭氧浓度适中的几周时间里,环境气溶胶中的有机部分在本质上绝大多数是二次生成的,并且SOA是里弗赛德PM1气溶胶的单一最大成分。在中午时段观察到SOA/OA的平均贡献率为70 - 90%,而在早晨交通高峰期观察到SOA的最小贡献率约为45%。这些结果与之前整个洛杉矶盆地对SOA的估算结果相反,之前的报告称,除了在严重的光化学烟雾事件期间,SOA低于一次有机气溶胶(OA)。讨论了这些差异的可能原因。