Luo Yuehan, Zhao Tianliang, Meng Kai, Zhang Lei, Wu Ming, Bai Yongqing, Kumar Kanike Raghavendra, Cheng Xinghong, Yang Qingjian, Liang Dingyuan
Collaborative Innovation Center on Forecast and Evaluation of Meteorological Disasters, Key Laboratory of Aerosol-Cloud-Precipitation of China Meteorological Administration, Nanjing University of Information Science and Technology, Nanjing 210044, China.
Collaborative Innovation Center on Forecast and Evaluation of Meteorological Disasters, Key Laboratory of Aerosol-Cloud-Precipitation of China Meteorological Administration, Nanjing University of Information Science and Technology, Nanjing 210044, China.
Sci Total Environ. 2024 Nov 10;950:175340. doi: 10.1016/j.scitotenv.2024.175340. Epub 2024 Aug 6.
Ozone (O) pollution with excessive near-surface O levels has been an important environmental issue in China, although the anthropogenic emission reductions (AER) have improved air quality since 2013. In this study, we investigated the sensitivities of atmospheric chemical environment with the urban and rural changes to the AER targeting a typical O pollution episode over North China in summer 2019, by conducting two WRF-Chem simulation experiments under two scenarios of anthropogenic emission inventories of years 2012 and 2019 with the meteorological conditions in the 2019 summertime O pollution episode for excluding the meteorological impacts on O pollution. The results show that the unbalanced AER aroused more serious O pollution in urban and rural areas. The intense NO reduction was responsible for the significant increments of urban O, while the falling NO and NO synergistically devoted to the slight O variations in rural areas. Induced by the recent-year AER, the urban O production was governed by VOCs-limited and transition regime, whereas the NOx-limited regime dominated over rural areas in North China. Also, the AER reinforced the atmospheric oxidation capacity with the elevations of atmospheric oxidants O and ROx radicals, strengthening the chemical conversions to secondary inorganic particles. In both urban and rural areas, the sharp drop in SO caused a decrease in sulfate fraction, while the enhanced AOC accelerated the transformation to nitrate even when NOx was reduced. The AER induced nitrate to occupy the principal position in secondary PM in urban and rural areas. The AER promoted daytime and suppressed nighttime the nitrate production in urban areas, and more vigorous conversion of secondary aerosols were found in rural areas with much lower AOC increments. This study provides insights from a case study over North China in distinct responses of urban and rural O pollution with secondary particle changes to AER in urban and rural atmospheric environment changes, with implications for an effective abatement strategy on O pollution.
尽管自2013年以来人为排放减少(AER)改善了空气质量,但近地表臭氧(O₃)污染且O₃水平过高一直是中国的一个重要环境问题。在本研究中,我们针对2019年夏季中国北方一次典型的O₃污染事件,通过在两种人为排放清单情景(2012年和2019年)下进行两次WRF-Chem模拟实验,并采用2019年夏季O₃污染事件期间的气象条件以排除气象因素对O₃污染的影响,研究了城乡变化下大气化学环境对AER的敏感性。结果表明,不均衡的AER在城乡地区引发了更严重的O₃污染。城市中NO大幅减少导致O₃显著增加,而农村地区NO和NO₂协同下降导致O₃略有变化。受近年来AER的影响,城市O₃生成受挥发性有机物(VOCs)限制和过渡状态控制,而华北农村地区则以氮氧化物(NOₓ)限制状态为主。此外,AER通过提高大气氧化剂O₃和ROₓ自由基的含量增强了大气氧化能力,强化了向二次无机颗粒物的化学转化。在城乡地区,SO₂的急剧下降导致硫酸盐比例降低,而增强的大气氧化能力(AOC)即使在NOₓ减少时也加速了向硝酸盐的转化。AER促使硝酸盐在城乡地区的二次颗粒物中占据主导地位。AER促进了城市地区白天硝酸盐的生成并抑制了夜间生成,而在AOC增量低得多的农村地区发现二次气溶胶的转化更为活跃。本研究通过对中国北方的一个案例研究,揭示了城乡O₃污染对AER以及城乡大气环境变化中二次颗粒物变化的不同响应,对制定有效的O₃污染减排策略具有启示意义。