Enhanced photochemical formation of secondary organic aerosols during the COVID-19 lockdown in Northern China

被引:32
作者
Meng, Jingjing [1 ]
Li, Zheng [1 ]
Zhou, Ruiwen [1 ]
Chen, Min [1 ]
Li, Yuanyuan [1 ]
Yi, Yanan [1 ]
Ding, Zhijian [2 ]
Li, Hongji [3 ]
Yan, Li [4 ]
Hou, Zhanfang [1 ]
Wang, Gehui [2 ]
机构
[1] Liaocheng Univ, Sch Environm & Planning, Liaocheng 252000, Shandong, Peoples R China
[2] East China Normal Univ, Sch Geog Sci, Key Lab Geog Informat Sci, Minist Educ, Shanghai 200062, Peoples R China
[3] Jilin Normal Univ, Coll Environm Sci & Engn, Siping 136000, Peoples R China
[4] Chinese Acad Environm Planning, Beijing 100012, Peoples R China
基金
美国国家科学基金会;
关键词
Oxalic acid; Glyoxal and methyglyoxal; Ozone; Formation mechanisms; COVID-19; lockdown; ATMOSPHERIC OXALIC-ACID; DICARBOXYLIC-ACIDS; ALPHA-DICARBONYLS; SINGLE-PARTICLE; OXOCARBOXYLIC ACIDS; MOLECULAR-DISTRIBUTION; KETOCARBOXYLIC ACIDS; FORMATION MECHANISM; MIXING STATE; LIQUID WATER;
D O I
10.1016/j.scitotenv.2020.143709
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
To eliminate the spread of a novel coronavirus breaking out in the end of 2019 (COVID-19), the Chinese government has implemented a nationwide lockdown policy after the Chinese lunar New Year of 2020, resulting in a sharp reduction in air pollutant emissions. To investigate the impact of the lockdown on aerosol chemistry, the number fraction, size distribution and formation process of oxalic acid (C-2) containing particles and its precursors were studied using a single particle aerosolmass spectrometer (SPAMS) at the urban site of Liaocheng in the North China Plain (NCP). Our results showed that five air pollutants (i.e., PM2.5, PM10, SO2, NO2, and CO) decreased by 30.0-59.8% during the lockdown compared to those before the lockdown, while O-3 increased by 63.9% during the lockdown mainly due to the inefficient titration effect of O-3 via NO reduction. The increased O-3 concentration can boost the atmospheric oxidizing capacity and further enhance the formation of secondary organic aerosols, thereby significantly enhancing the C-2 particles and its precursors as observed during the lockdown. Before the lockdown, C-2 particles were significantly originated from biomass burning emissions and their subsequent aqueous-phase oxidation. The hourly variation patterns and correlation analysis before the lockdown suggested that relative humidity (RH) and aerosol liquid water content (ALWC) played a key role in the formation of C-2 particles and the increased aerosol acidity can promote the conversion of precursors such as glyoxal (Gly) and methyglyoxal (mGly) into C-2 particles in the aqueous phase. RH and ALWC decreased sharply but O-3 concentration and solar radiation increased remarkably during the lockdown, the O-3-dominated photochemical pathways played an important role in the formation of C-2 particles in which aerosol acidity was ineffective. Our study indicated that air pollution treatment sponges on a joint-control and balanced strategy for controlling numerous pollutants. (C) 2020 Elsevier B.V. All rights reserved.
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页数:10
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共 60 条
  • [1] [Anonymous], 2018, ATMOSPHERIC CHEM PHY, DOI DOI 10.1007/JHEP11(2018)001
  • [2] Does lockdown reduce air pollution? Evidence from 44 cities in northern China
    Bao, Rui
    Zhang, Acheng
    [J]. SCIENCE OF THE TOTAL ENVIRONMENT, 2020, 731
  • [3] Mixing state of biomass burning particles by single particle aerosol mass spectrometer in the urban area of PRD, China
    Bi, Xinhui
    Zhang, Guohua
    Li, Lei
    Wang, Xinming
    Li, Mei
    Sheng, Guoying
    Fu, Jiamo
    Zhou, Zhen
    [J]. ATMOSPHERIC ENVIRONMENT, 2011, 45 (20) : 3447 - 3453
  • [4] Saturation Vapor Pressures and Transition Enthalpies of Low-Volatility Organic Molecules of Atmospheric Relevance: From Dicarboxylic Acids to Complex Mixtures
    Bilde, Merete
    Barsanti, Kelley
    Booth, Murray
    Cappa, Christopher D.
    Donahue, Neil M.
    Emanuelsson, Eva U.
    McFiggans, Gordon
    Krieger, Ulrich K.
    Marcolli, Claudia
    Tropping, David
    Ziemann, Paul
    Barley, Mark
    Clegg, Simon
    Dennis-Smither, Benjamin
    Hallquist, Mattias
    Hallquist, Asa M.
    Khlystov, Andrey
    Kulmala, Markku
    Mogensen, Ditte
    Percival, Carl J.
    Pope, Francis
    Reid, Jonathan P.
    da Silva, M. A. V. Ribeiro
    Rosenoern, Thomas
    Salo, Kent
    Soonsin, Vacharapom Pia
    Yli-Juuti, Taina
    Prisle, Nonne L.
    Pagels, Joakim
    Rarey, Juergen
    Zardini, Alessandro A.
    Riipinen, Ilona
    [J]. CHEMICAL REVIEWS, 2015, 115 (10) : 4115 - 4156
  • [5] Link between isoprene and secondary organic aerosol (SOA): Pyruvic acid oxidation yields low volatility organic acids in clouds
    Carlton, AG
    Turpin, BJ
    Lim, HJ
    Altieri, KE
    Seitzinger, S
    [J]. GEOPHYSICAL RESEARCH LETTERS, 2006, 33 (06)
  • [6] Atmospheric oxalic acid and SOA production from glyoxal: Results of aqueous photooxidation experiments
    Carlton, Annmarie G.
    Turpin, Barbara J.
    Altieri, Katye E.
    Seitzinger, Sybil
    Reff, Adam
    Lim, Ho-Jin
    Ervens, Barbara
    [J]. ATMOSPHERIC ENVIRONMENT, 2007, 41 (35) : 7588 - 7602
  • [7] Influence of COVID-19 Event on Air Quality and their Association in Mainland China
    Chen, Qi-Xiang
    Huang, Chun-Lin
    Yuan, Yuan
    Tan, He-Ping
    [J]. AEROSOL AND AIR QUALITY RESEARCH, 2020, 20 (07) : 1541 - 1551
  • [8] Mixing state of oxalic acid containing particles in the rural area of Pearl River Delta, China: implications for the formation mechanism of oxalic acid
    Cheng, Chunlei
    Li, Mei
    Chan, Chak K.
    Tong, Haijie
    Chen, Changhong
    Chen, Duohong
    Wu, Dui
    Li, Lei
    Wu, Cheng
    Cheng, Peng
    Gao, Wei
    Huang, Zhengxu
    Li, Xue
    Zhang, Zhijuan
    Fu, Zhong
    Bi, Yanru
    Zhou, Zhen
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2017, 17 (15) : 9519 - 9533
  • [9] Size-resolved airborne particulate oxalic and related secondary organic aerosol species in the urban atmosphere of Chengdu, China
    Cheng, Chunlei
    Wang, Gehui
    Meng, Jingjing
    Wang, Qiyuan
    Cao, Junji
    Li, Jianjun
    Wang, Jiayuan
    [J]. ATMOSPHERIC RESEARCH, 2015, 161 : 134 - 142
  • [10] Thermodynamic model of the system H+-NH4+-SO42--NO3--H2O at tropospheric temperatures
    Clegg, SL
    Brimblecombe, P
    Wexler, AS
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (12) : 2137 - 2154