Key Laboratory of Aerosol Chemistry and Physics, State Key Laboratory of Loess and Quaternary Geology, CAS Center for Excellence in Quaternary Science and Global Change, Institute of Earth and Environment, Chinese Academy of Sciences, Xi'an 710061, China.
Key Laboratory of Aerosol Chemistry and Physics, State Key Laboratory of Loess and Quaternary Geology, CAS Center for Excellence in Quaternary Science and Global Change, Institute of Earth and Environment, Chinese Academy of Sciences, Xi'an 710061, China.
Sci Total Environ. 2020 May 15;717:137190. doi: 10.1016/j.scitotenv.2020.137190. Epub 2020 Feb 8.
Sulfate and nitrate from secondary reactions remain as the most abundant inorganic species in atmospheric particle matter (PM). Their formation is initiated by oxidation (either in gas phase or particle phase), followed by neutralization reaction primarily by NH, or by other alkaline species such as alkaline metal ions if available. The different roles of NH and metal ions in neutralizing HSO or HNO, however, are seldom investigated. Here we conducted semi-continuous measurements of SO, NO, NH, and their gaseous precursors, as well as alkaline metal ions (Na, K, Ca, and Mg) in wintertime Beijing. Analysis of aerosol acidity (estimated from a thermodynamic model) indicated that preferable sulfate formation was related to low pH conditions, while high pH conditions promote nitrate formation. Data in different mass fraction ranges of alkaline metal ions showed that in some ranges the role of NH was replaced by alkaline metal ions in the neutralization reaction of HSO and HNO to form particulate SO and NO. The relationships between mass fractions of SO and NO in those ranges of different alkaline metal ion content also suggested that alkaline metal ions participate in the competing neutralization reaction of sulfate and nitrate. The implication of the current study is that in some regions the chemistry to incorporate sulfur and nitrogen into particle phase might be largely affected by desert/fugitive dust and sea salt, besides NH. This implication is particularly relevant in coastal China and those areas with strong influence of dust storm in the North China Plain (NCP), both of which host a number of megacities with deteriorating air quality.
硫酸盐和硝酸盐来自二次反应,仍然是大气颗粒物(PM)中最丰富的无机物质。它们的形成是由氧化(无论是在气相还是在颗粒相中)引发的,随后主要通过 NH 进行中和反应,或者在有条件的情况下通过其他碱性物质如碱性金属离子进行中和反应。然而,NH 和金属离子在中和 HSO 和 HNO 方面的不同作用很少被研究。在这里,我们在冬季的北京进行了 SO、NO、NH 及其气态前体以及碱性金属离子(Na、K、Ca 和 Mg)的半连续测量。气溶胶酸度的分析(根据热力学模型估计)表明,优先形成硫酸盐与低 pH 条件有关,而高 pH 条件则促进硝酸盐的形成。在不同碱性金属离子质量分数范围内的数据表明,在某些范围内,NH 在 HSO 和 HNO 的中和反应中被碱性金属离子取代,形成颗粒态 SO 和 NO。在不同碱性金属离子含量范围内 SO 和 NO 质量分数之间的关系也表明,碱性金属离子参与了硫酸盐和硝酸盐的竞争中和反应。本研究的意义在于,在某些地区,将硫和氮纳入颗粒相的化学过程可能在很大程度上受到沙漠/扬尘和海盐的影响,而不仅仅是 NH。这一意义在中国沿海地区和中国北方平原(NCP)受沙尘暴影响强烈的地区尤为重要,这些地区拥有许多空气质量不断恶化的特大城市。