分摊
海盐
气溶胶
环境科学
环境化学
氯化物
大气科学
化学
气象学
地理
地质学
政治学
法学
有机化学
作者
Xiankang Wu,Qing Kong,Yang Lan,Judy Sng,Liya E. Yu
标识
DOI:10.1021/acs.est.3c10142
摘要
Sea salt (ss) aerosols in PM2.5 are often quantified through source apportionment by applying sodium (Na+) and chloride (Cl–) as the markers, but both markers can be substantially emitted from anthropogenic sources. In this study, we differentiate ss from nonss (nss) portions of Na+ and Cl– to better apportion PM2.5 in a coastal tropical urban environment. Size-resolved ionic profiles accounting for Cl– depletion of aged ss were applied to 162-day measurements during 2012 and 2018–2019. Results show that the nss (likely anthropogenic) portions, on average, account for 50–80% of total Na+ and Cl– in submicron aerosols (PM1). This corresponds to up to 2.5 μg/m3 of ss in submicron aerosols that can be ∼10 times overestimated if one attributes all Na+ and Cl– in PM1 to ss. Employing the newly speciated ss- and nss-portions of Na+ and Cl– to source apportionment of urban PM2.5 via positive matrix factorization uncovers a new source of transported anthropogenic emissions during the southwest monsoon, contributing to 12–15% of PM2.5. This increases anthropogenic PM2.5 by ≥19% and reduces ss-related PM2.5 by >30%. In addition to demonstrating Cl– depletion (aging) in submicron aerosols and quantifying ssNa+, nssNa+, ssCl–, as well as nssCl– therein, the refined PM2.5 apportionment resolves new insights on PM2.5 of anthropogenic origins in urban environments, useful to facilitate policy making.
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