Chang Xing, Zheng Haotian, Zhao Bin, Yan Chao, Jiang Yueqi, Hu Ruolan, Song Shaojie, Dong Zhaoxin, Li Shengyue, Li Zeqi, Zhu Yun, Shi Hongrong, Jiang Zhe, Xing Jia, Wang Shuxiao
State Key Joint Laboratory of Environmental Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 100084, China.
State Environmental Protection Key Laboratory of Sources and Control of Air Pollution Complex, Beijing 100084, China.
Environ Sci Technol. 2023 Apr 11;57(14):5521-5531. doi: 10.1021/acs.est.2c06914. Epub 2023 Mar 31.
During the COVID-19 lockdown in early 2020, observations in Beijing indicate that secondary organic aerosol (SOA) concentrations increased despite substantial emission reduction, but the reasons are not fully explained. Here, we integrate the two-dimensional volatility basis set into a state-of-the-art chemical transport model, which unprecedentedly reproduces organic aerosol (OA) components resolved by the positive matrix factorization based on aerosol mass spectrometer observations. The model shows that, for Beijing, the emission reduction during the lockdown lowered primary organic aerosol (POA)/SOA concentrations by 50%/18%, while deteriorated meteorological conditions increased them by 30%/119%, resulting in a net decrease in the POA concentration and a net increase in the SOA concentration. Emission reduction and meteorological changes both led to an increased OH concentration, which accounts for their distinct effects on POA and SOA. SOA from anthropogenic volatile organic compounds and organics with lower volatility contributed 28 and 62%, respectively, to the net SOA increase. Different from Beijing, the SOA concentration decreased in southern Hebei during the lockdown because of more favorable meteorology. Our findings confirm the effectiveness of organic emission reductions and meanwhile reveal the challenge in controlling SOA pollution that calls for large organic precursor emission reductions to rival the adverse impact of OH increase.
在2020年初新冠疫情封锁期间,北京的观测结果表明,尽管排放量大幅减少,但二次有机气溶胶(SOA)浓度却有所上升,不过其原因尚未完全明确。在此,我们将二维挥发性基组整合到一个先进的化学传输模型中,该模型首次再现了基于气溶胶质谱观测通过正定矩阵因子分解解析出的有机气溶胶(OA)成分。模型显示,对于北京而言,封锁期间的排放减少使一次有机气溶胶(POA)/SOA浓度分别降低了50%/18%,而气象条件恶化使其分别增加了30%/119%,导致POA浓度净下降,SOA浓度净上升。排放减少和气象变化均导致OH浓度增加,这解释了它们对POA和SOA产生不同影响的原因。人为挥发性有机化合物和挥发性较低的有机物产生的SOA分别占SOA净增加量的28%和62%。与北京不同,由于气象条件更为有利,封锁期间河北南部的SOA浓度有所下降。我们的研究结果证实了有机排放减少的有效性,同时揭示了控制SOA污染面临的挑战,即需要大幅减少有机前体排放以抵消OH增加带来的不利影响。