State Environmental Protection Key Laboratory of Urban Ambient Air Particulate Matter Pollution Prevention and Control, Tianjin Key Laboratory of Urban Transport Emission Research, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China; CMA-NKU Cooperative Laboratory for Atmospheric Environment-Health Research (CLAER), College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China.
Guangzhou Hexin Instrument Co., Ltd, Guangzhou 510530, China.
Environ Int. 2023 Feb;172:107786. doi: 10.1016/j.envint.2023.107786. Epub 2023 Jan 30.
Ground-level ozone (O) pollution has received widespread attention because its rising trend and adverse ecological impacts. However, the extremely strong photochemical reactions of its precursor volatile organic compounds (VOCs) increase the difficulty of reducing VOCs emissions to alleviate O. Here, we carried out a one-year comprehensive observation in two representative cities, Tianjin (TJ, Northern China) and Guangzhou (GZ, Southern China). By revealing the concentration characteristics of three different types of VOCs, i.e., initial VOCs without photochemical reaction (In-VOCs), consumed VOCs (C-VOCs), and measured VOCs after the reaction (M-VOCs), we elucidated the important role of C-VOCs in the formation of O. Although the overall trends were similar in both cities, the average concentration level of VOCs in GZ was 8.2 ppbv higher than that in TJ, and the photochemical loss of VOCs was greater by 2.2 ppbv. In addition, various drivers affecting O generation from C-VOCs were specifically explored, and it was found that most alkenes of TJ were key substances for rapid O formation compared to aromatics of GZ. Meanwhile, favorable meteorological conditions such as high temperature (T > 31 °C in TJ, and T > 33 °C in GZ), low relative humidity (56% in TJ and 45% in GZ), and stable atmospheric environment (proper pressure and gentle wind speed) also contribute to the generation of O. More importantly, we combined chemical kinetics and receptor model to quantify the three-type VOCs source contributions and assess the potential impact of C-VOCs sources on O production, thus proposing environmental abatement technologies corresponding to the three types of VOCs. The differences in the comparison results of the three-type VOCs highlight the need to reduce O pollution from C-VOCs sources, which provides insights for future clean air policies development.
地面臭氧(O)污染因其上升趋势和对生态的不利影响而受到广泛关注。然而,其前体挥发性有机化合物(VOCs)的极强光化学反应增加了减少 VOCs 排放以缓解 O 的难度。在这里,我们在两个具有代表性的城市天津(TJ,中国北方)和广州(GZ,中国南方)进行了为期一年的综合观测。通过揭示三种不同类型 VOC 的浓度特征,即没有光化学反应的初始 VOC(In-VOCs)、消耗的 VOC(C-VOCs)和反应后测量的 VOC(M-VOCs),我们阐明了 C-VOCs 在 O 形成中的重要作用。尽管两个城市的总体趋势相似,但 GZ 的 VOC 平均浓度水平比 TJ 高 8.2 ppbv,VOC 的光化学损失高 2.2 ppbv。此外,还专门探讨了影响 C-VOCs 产生 O 的各种驱动因素,发现与 GZ 的芳烃相比,TJ 的大多数烯烃是快速形成 O 的关键物质。同时,有利的气象条件,如高温(TJ 时>31°C,GZ 时>33°C)、低相对湿度(TJ 时 56%,GZ 时 45%)和稳定的大气环境(适当的压力和微风速)也有助于 O 的生成。更重要的是,我们结合化学动力学和受体模型来量化三种类型 VOC 的源贡献,并评估 C-VOCs 源对 O 生成的潜在影响,从而提出了针对三种类型 VOC 的环境减排技术。三种类型 VOC 的比较结果的差异突出了需要减少 C-VOCs 源的 O 污染,这为未来清洁空气政策的制定提供了思路。