Ye Zhao-Lian, Qu Zhen-Xiu, Ma Shuai-Shuai, Gai Xin-Lei
School of Chemical and Environmental Engineering, Jiangsu University of Technology, Changzhou 213001, China.
Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, School of Environmental Science and Engineering, Nanjing University of Information Science & Technology, Nanjing 210044, China.
Huan Jing Ke Xue. 2018 Aug 8;39(8):3954-3964. doi: 10.13227/j.hjkx.201712236.
Liquid water (cloud/fog droplets and aerosols) is ubiquitous in the atmosphere and can provide an important reaction media for aqueous-phase chemical reactions. Gaseous precursors (mainly VOCs) or their gas-phase initial or first-generation oxidation products (including intermediate-volatility and semi-volatile organic compounds; I/SVOCs) can undergo chemical reactions in the atmospheric condensed phase (aqueous phase) to form low-volatility, highly oxidized organic matter[e.g., some key tracer species such as organosulfates (OSs) and organonitrogens (ONs)]. These products largely remain in the particle phase upon water evaporation and are referred to as aqueous secondary organic aerosols (aqSOAs). aqSOAs have been emerging as a research hot topic in atmospheric chemistry, as they can contribute significantly to OAs and thus have important impacts on the environment, climate, and human health. Despite considerable progress, so far, aqSOAs remain poorly understood owing to their complex formation mechanisms. In this review, we focus mainly on the relevant research results on the SOAs formed in aerosol water-aqueous aerosol SOAs (aaSOAs)-including gas-phase precursors, formation mechanisms, laboratory simulations, and field observations, as well as SOA yield and contribution to OAs. Meanwhile, we propose future directions regarding studies of sources and formation mechanisms of aaSOAs, including identification of unknown aaSOA precursors and tracer products, photosensitizer-triggered radical chemistry, formation pathways of OS and ON compounds, field observations and model simulations of aaSOAs.
液态水(云/雾滴和气溶胶)在大气中无处不在,可为水相化学反应提供重要的反应介质。气态前体(主要是挥发性有机化合物)或其气相初始或第一代氧化产物(包括中等挥发性和半挥发性有机化合物;I/SVOCs)可在大气凝聚相(水相)中发生化学反应,形成低挥发性、高度氧化的有机物[例如,一些关键示踪物种,如有机硫酸盐(OSs)和有机氮(ONs)]。这些产物在水蒸发后大多保留在颗粒相中,被称为水相二次有机气溶胶(aqSOAs)。aqSOAs已成为大气化学领域的一个研究热点,因为它们对有机气溶胶有显著贡献,从而对环境、气候和人类健康产生重要影响。尽管取得了相当大的进展,但迄今为止,由于其形成机制复杂,aqSOAs仍未得到充分理解。在这篇综述中,我们主要关注气溶胶水相中形成的二次有机气溶胶(aaSOAs)的相关研究成果——包括气相前体、形成机制、实验室模拟和实地观测,以及二次有机气溶胶的产率及其对有机气溶胶的贡献。同时,我们提出了关于aaSOAs来源和形成机制研究的未来方向,包括识别未知的aaSOA前体和示踪产物、光敏剂引发的自由基化学、OS和ON化合物的形成途径、aaSOAs的实地观测和模型模拟。