State Key Joint Laboratory of Environmental Simulation and Pollution Control, BIC-ESAT and IJRC, College of Environmental Sciences and Engineering, Peking University, Beijing 100871, China.
Department of Civil and Environmental Engineering, Faculty of Science and Technology, University of Macau, Taipa, Macau 999078, China.
Environ Sci Technol. 2021 Jun 1;55(11):7276-7286. doi: 10.1021/acs.est.0c08591. Epub 2021 May 19.
Vehicle emissions are an important source of urban particular matter. To investigate the secondary organic aerosol (SOA) formation potential of real-world vehicle emissions, we exposed on-road air in Beijing to hydroxyl radicals generated in an oxidation flow reactor (OFR) under high-NO conditions on-board a mobile laboratory and characterized SOA and their precursors with a suite of state-of-the-art instrumentation. The OFR produced 10-170 μg m of SOA with a maximum SOA formation potential of 39-50 μg m ppmv CO that occurred following an integrated OH exposure of (1.3-2.0) × 10 molecules cm s. The results indicate relatively shorter photochemical ages for maximum SOA production than previous OFR results obtained under low-NO conditions. Such timescales represent the balance of functionalization and fragmentation, possibly resulting in different spatial distributions of SOA in different seasons as the oxidant level changes. The detected precursors may explain as much as 13% of the observed SOA with the remaining plausibly contributed by the oxidation of undetected intermediate-volatility organic compounds. Extrapolation of the results suggests an annual SOA production rate of 0.78 Tg yr from mobile gasoline sources in China, highlighting the importance of effective regulation of gaseous vehicular precursors to improve air quality in the future.
车辆排放是城市颗粒物的一个重要来源。为了研究实际车辆排放的二次有机气溶胶(SOA)形成潜力,我们在一辆移动实验室的车载氧化流动反应器(OFR)中,在高氮条件下用羟基自由基对北京的道路空气进行暴露,并使用一系列最先进的仪器对 SOA 及其前体进行了表征。OFR 产生了 10-170 μg m 的 SOA,最大 SOA 形成潜力为 39-50 μg m ppmv CO,这是在(1.3-2.0)×10 个分子 cm s 的综合 OH 暴露后发生的。结果表明,与在低氮条件下获得的 OFR 结果相比,最大 SOA 生成的光化学年龄相对较短。这些时间尺度代表了功能化和碎片化的平衡,可能导致在不同季节氧化剂水平变化时 SOA 的空间分布不同。所检测到的前体可能解释了高达 13%的观察到的 SOA,其余部分可能是由未检测到的中挥发性有机化合物的氧化产生的。结果的推断表明,中国移动汽油源每年的 SOA 生成速率为 0.78 Tg yr,这突出了有效控制气态车辆前体以改善未来空气质量的重要性。