2014
DOI: 10.6023/a14040254
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Comparison of Secondary Organic Aerosol Estimation Methods

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Cited by 16 publications
(7 citation statements)
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“…It can be seen that the PM 2.5 concentration was highly linearly correlated with the secondary species (P < 0.01). These chemical species are directly indicative of secondary chemistry: sulfate is mainly converted from atmospheric SO 2 primarily emitted from coal combustion (Seinfeld and Pandis, 2016), nitrate originates from NO x emitted mainly from vehicle exhaust and power plants (Seinfeld and Pandis, 2016), and secondary organic carbon (SOC), as an indicator of SOA, derives from complex gaseous precursors (Hallquist et al, 2009). Specifically, PM 2.5 showed a higher correlation with SIA (P < 0.001) than with SOA (P < 0.01), probably due to the higher contribution of SIA to SA than SOA (Fig.…”
Section: Uncertainty Analysis In the Estimation Of Secondary Aerosolsmentioning
confidence: 99%
“…It can be seen that the PM 2.5 concentration was highly linearly correlated with the secondary species (P < 0.01). These chemical species are directly indicative of secondary chemistry: sulfate is mainly converted from atmospheric SO 2 primarily emitted from coal combustion (Seinfeld and Pandis, 2016), nitrate originates from NO x emitted mainly from vehicle exhaust and power plants (Seinfeld and Pandis, 2016), and secondary organic carbon (SOC), as an indicator of SOA, derives from complex gaseous precursors (Hallquist et al, 2009). Specifically, PM 2.5 showed a higher correlation with SIA (P < 0.001) than with SOA (P < 0.01), probably due to the higher contribution of SIA to SA than SOA (Fig.…”
Section: Uncertainty Analysis In the Estimation Of Secondary Aerosolsmentioning
confidence: 99%
“…后续增长过程主要包括气态物质如有机物凝结、均 相反应以及颗粒物模态内的碰并. 气态硫酸、无机氨、 有机胺等物质可以通过形成硫酸盐、有机酸盐、有机胺 盐等参与颗粒物增长 [30~32] , 外场研究也印证了二次有 机组分在颗粒物中占到较大比重 [33,34] , 然而有机物贡献 后续增长的机制仍然存在诸多疑问 [25] ,…”
Section: 新粒子生成和增长机制及其环境影响unclassified
“…It remains difficult to quantify the contribution of precursors in the ambient environment. Several field‐based methods have been developed to estimate the amount of SOA, including the tracer‐yield method (Guo et al, 2012; Kleindienst et al, 2007), the nonprimary organic carbon (OC) method (the receptor model) (Heo et al, 2015; Yuan et al, 2006; Zheng et al, 2002), the non–biomass burning water‐soluble organic carbon method (Weber et al, 2007) and the elemental carbon (EC)‐tracer method (or the OC/EC ratio method) [Cao et al, 2007; Song Guo et al, 2014; Turpin & Huntzicker, 1995; Zhang et al, 2008]. Among these methods, the receptor model can be used to apportion SOA in submicron particulate matter (PM 1.0 ) at a high time resolution from aerosol mass spectrometry (AMS) data (Hu et al, 2013; Huang et al, 2012; Huang et al, 2014; Li et al, 2015; Sun et al, 2013; Zhang, 2005), while the tracer‐yield method provides the only way of identifying precursors of SOA but with a low time resolution due to the complexity of tracer measurements.…”
Section: Introductionmentioning
confidence: 99%