Global PM2.5 and secondary organic aerosols (SOA) levels with sectorial contribution to anthropogenic and biogenic SOA formation

被引:5
|
作者
Azmi S. [1 ]
Sharma M. [1 ]
机构
[1] Department of Civil Engineering and Centre for Environmental Science and Engineering, Indian Institute of Technology Kanpur, Uttar Pradesh, Kanpur
关键词
Anthropogenic; Biogenic; Coal and non-coal industry; Global PM[!sub]2.5[!/sub; Secondary organic aerosols;
D O I
10.1016/j.chemosphere.2023.139195
中图分类号
学科分类号
摘要
This study estimates global PM2.5 and anthropogenic and biogenic Secondary Organic Aerosols (a-SOA and b-SOA) and sources contributing to their formation. The global landscape was divided into eleven domains (North America (NAM); South America (SAM); Europe (EUR); North Africa and Middle East (NAF); Equatorial Africa (EAF); South of Africa (SAF); Russia and Central Asia (RUS); Eastern Asia (EAS); South Asia (SAS); Southeast Asia (SEA) and Australia (AUS)) and 46 cities based on varying populations. Three inventories for global emissions were considered: Community Emissions Data System, Model of Emission of Gases and Aerosol, and Global Fire Emissions Database. WRF-Chem model coupled with atmospheric reactions and the secondary organic aerosol model was employed for estimating PM2.5, a-SOA, and b-SOA for 2018. No city attained WHO's annual PM2.5 guideline of 5 μg/m3. Delhi, Dhaka, and Kolkata (63–92 μg/m3) in south Asia were the most polluted, and seven cities (mostly in EUR and NAM) met the WHO target IV (10 μg/m3). The highest SOA levels (2–9 μg/m3) were in the cities of SAS and Africa, but with a low SOA contribution to PM2.5 (3–22%). However, the low levels of SOA (1–3 μg/m3) in EUR and NAM had a higher contribution of SOA to PM2.5 (20–33%). b-SOA were consistent with the region's vegetation and forest cover. The SOA contribution was dominated by residential emissions in all domains (except in the NAF and AUS) (maximum in SAS). The non-coal industry was the second highest contributor (except in EAF, NAF, and AUS) and EUR had the maximum contribution from agriculture and transport. Globally, residential and industry (non-coal and coal) sectors showed the maximum contribution to SOA, with a-SOA and b-SOA being nearly equal. Ridding of biomass and residential burning of solid fuel is the single most action benefiting the PM2.5 and SOA concerns. © 2023 Elsevier Ltd
引用
收藏
相关论文
共 50 条
  • [1] Formation of anthropogenic secondary organic aerosol (SOA) and its influence on biogenic SOA properties
    Emanuelsson, E. U.
    Hallquist, M.
    Kristensen, K.
    Glasius, M.
    Bohn, B.
    Fuchs, H.
    Kammer, B.
    Kiendler-Scharr, A.
    Nehr, S.
    Rubach, F.
    Tillmann, R.
    Wahner, A.
    Wu, H. -C.
    Mentel, Th. F.
    ATMOSPHERIC CHEMISTRY AND PHYSICS, 2013, 13 (05) : 2837 - 2855
  • [2] Major sources of PM2.5 organic aerosols in Europe: Predominance of biomass burning and secondary organic aerosols (SOA)
    Gelencser, A.
    May, B.
    Simpson, D.
    Sanchez-Ochoa, A.
    Kasper-Giebl, A.
    Puxbaum, H.
    Caseiro, A.
    Pio, C.
    Legrand, M.
    GEOCHIMICA ET COSMOCHIMICA ACTA, 2009, 73 (13) : A425 - A425
  • [3] Inflammatory responses to secondary organic aerosols (SOA) generated from biogenic and anthropogenic precursors
    Tuet, Wing Y.
    Chen, Yunle
    Fok, Shierly
    Champion, Julie A.
    Ng, Nga L.
    ATMOSPHERIC CHEMISTRY AND PHYSICS, 2017, 17 (18) : 11423 - 11440
  • [4] Global health burden of ambient PM2.5 and the contribution of anthropogenic black carbon and organic aerosols
    Chowdhury, Sourangsu
    Pozzer, Andrea
    Haines, Andy
    Klingmueller, Klaus
    Muenzel, Thomas
    Paasonen, Pauli
    Sharma, Arushi
    Venkataraman, Chandra
    Lelieveld, Jos
    ENVIRONMENT INTERNATIONAL, 2022, 159
  • [5] Anthropogenic and biogenic organic compounds in summertime fine aerosols (PM2.5) in Beijing, China
    Yang, Fan
    Kawamura, Kimitaka
    Chen, Jing
    Ho, Kinfai
    Lee, Shuncheng
    Gao, Yuan
    Cui, Long
    Wang, Tieguan
    Fu, Pingqing
    ATMOSPHERIC ENVIRONMENT, 2016, 124 : 166 - 175
  • [6] Experimental data on SOA formation from mixtures of anthropogenic and biogenic organic compounds
    Vivanco, M. G.
    Santiago, M.
    Sanchez, M.
    Clavero, M. A.
    Borras, E.
    Rodenas, M.
    Alacreu, F.
    Vazquez, M.
    Clemente, E.
    Porras, R.
    Munoz, A.
    Stein, A.
    ATMOSFERA, 2013, 26 (01): : 59 - 73
  • [7] Seasonal variation, source contribution, and impact factors of biogenic organic aerosols in PM2.5 in Nanjing, China
    Cao, Maoyu
    Chen, Mindong
    Ge, Pengxiang
    Cui, Yan
    Li, Wenjing
    SCIENCE OF THE TOTAL ENVIRONMENT, 2022, 843
  • [8] Molecular compositions and affecting factors of biogenic SOA in PM2.5 from Mount Taishan during the summer
    Yi, Ya-Nan
    Yao, Zheng-Zheng
    Hou, Zhan-Fang
    Zhou, Rui-Wen
    Li, Zheng
    Liu, Xiao-Di
    Wang, Ya-Chen
    Fu, Meng-Xuan
    Wei, Ben-Jie
    Yan, Li
    Meng, Jing-Jing
    Zhongguo Huanjing Kexue/China Environmental Science, 2020, 40 (08): : 3352 - 3359
  • [9] Identification of biogenic and anthropogenic components of secondary organic aerosol (SOA) by nuclear magnetic resonance spectroscopy
    Finessi, E.
    Decesari, S.
    Baltensperger, U.
    Mentel, Th. F.
    Facchini, M. C.
    GEOCHIMICA ET COSMOCHIMICA ACTA, 2009, 73 (13) : A377 - A377
  • [10] Estimations of primary and secondary organic carbon formation in PM2.5 aerosols of Santiago City, Chile
    Seguel A., Rodrigo
    Morales S., Raul G. E.
    Leiva G., Manuel A.
    ATMOSPHERIC ENVIRONMENT, 2009, 43 (13) : 2125 - 2131