Characteristics of PM2.5-bound secondary organic aerosol tracers in a coastal city in Southeastern China: Seasonal patterns and pollution identification. (15th September 2020)
- Record Type:
- Journal Article
- Title:
- Characteristics of PM2.5-bound secondary organic aerosol tracers in a coastal city in Southeastern China: Seasonal patterns and pollution identification. (15th September 2020)
- Main Title:
- Characteristics of PM2.5-bound secondary organic aerosol tracers in a coastal city in Southeastern China: Seasonal patterns and pollution identification
- Authors:
- Liu, Taotao
Hu, Baoye
Xu, Xinbei
Hong, Youwei
Zhang, Yanru
Wu, Xin
Xu, Lingling
Li, Mengren
Chen, Yanting
Chen, Xiaoqiu
Chen, Jinsheng - Abstract:
- Abstract: Secondary organic aerosol (SOA) plays an important role in global climate change and air quality, and SOA tracers most directly characterize the sources and formation mechanisms of SOA. Four seasons of observation of SOA tracers was carried out in a coastal city of southeastern China. Fourteen PM2.5 -bound SOA tracers, including isoprene (SOAI ), α/β-pinene (SOAM ), β-caryophyllene (SOAC ), and toluene (SOAA ), were measured using the GC–MS method. The concentrations of SOA tracers in Fuzhou were 25.9 ± 19.9 ng m −3 (SOAM ), 7.45 ± 8.53 ng m −3 (SOAI ), 3.15 ± 1.99 ng m −3 (SOAC ), and 2.63 ± 1.54 ng m −3 (SOAA ). The elevated SOAI concentration in summer was mainly controlled by high biogenic isoprene emission and strong oxidation, and biomass burning contributed strongly to DHOPA (SOAA ) in fall. SO4 2− and H + insitu had an increased impact on later-generation SOAI products and low-NOx SOAM products. Based on the ratio of MGA/MTLs and MBTCA/(PA + PNA), atmospheric oxidation capacity (Ox, =NO2 +O3 ) had a significant impact on the aerosol aging of SOA tracers. The increased proportions of low-NOx SOAI products were 3.23–7.21 times higher than those of high-NOx products from non-haze to haze periods, suggesting the influence of high SO4 2− concentration and RH on the reaction channel for SOAI formation. The percentages of later-generation SOAM products during RT were 2.46 times higher than those of first-generation products, suggesting the influence of aerosolAbstract: Secondary organic aerosol (SOA) plays an important role in global climate change and air quality, and SOA tracers most directly characterize the sources and formation mechanisms of SOA. Four seasons of observation of SOA tracers was carried out in a coastal city of southeastern China. Fourteen PM2.5 -bound SOA tracers, including isoprene (SOAI ), α/β-pinene (SOAM ), β-caryophyllene (SOAC ), and toluene (SOAA ), were measured using the GC–MS method. The concentrations of SOA tracers in Fuzhou were 25.9 ± 19.9 ng m −3 (SOAM ), 7.45 ± 8.53 ng m −3 (SOAI ), 3.15 ± 1.99 ng m −3 (SOAC ), and 2.63 ± 1.54 ng m −3 (SOAA ). The elevated SOAI concentration in summer was mainly controlled by high biogenic isoprene emission and strong oxidation, and biomass burning contributed strongly to DHOPA (SOAA ) in fall. SO4 2− and H + insitu had an increased impact on later-generation SOAI products and low-NOx SOAM products. Based on the ratio of MGA/MTLs and MBTCA/(PA + PNA), atmospheric oxidation capacity (Ox, =NO2 +O3 ) had a significant impact on the aerosol aging of SOA tracers. The increased proportions of low-NOx SOAI products were 3.23–7.21 times higher than those of high-NOx products from non-haze to haze periods, suggesting the influence of high SO4 2− concentration and RH on the reaction channel for SOAI formation. The percentages of later-generation SOAM products during RT were 2.46 times higher than those of first-generation products, suggesting the influence of aerosol aging during the regional transport. Both continental Asian outflow and biomass-burning plumes promoted precursor emissions and the formation process of SOA during the haze pollution events. These related findings help to understand the occurrence, sources and formation of SOA in coastal areas. Highlights: SO4 2− and H + insitu had an increased impact on low-NOx SOAI products and later-generation SOAM products. The HO2 channel was the main chemical reaction of SOA during haze periods. Biomass-burning plumes promoted precursor emissions and the formation of SOA during haze events with regional transport. … (more)
- Is Part Of:
- Atmospheric environment. Volume 237(2020)
- Journal:
- Atmospheric environment
- Issue:
- Volume 237(2020)
- Issue Display:
- Volume 237, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 237
- Issue:
- 2020
- Issue Sort Value:
- 2020-0237-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-09-15
- Subjects:
- Secondary organic aerosol (SOA) tracers -- PM2.5 -- Coastal area -- Air pollution -- Formation mechanisms
Air -- Pollution -- Periodicals
Air -- Pollution -- Meteorological aspects -- Periodicals
551.51 - Journal URLs:
- http://www.sciencedirect.com/web-editions/journal/13522310 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.atmosenv.2020.117710 ↗
- Languages:
- English
- ISSNs:
- 1352-2310
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1767.120000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 18806.xml