scholarly journals "Wintertime aerosol dominated by solid fuel burning emissions across Ireland: insight into the spatial and chemical variation of submicron aerosol" Chunshui Lin et al.

2019 ◽  
Author(s):  
Anonymous
2019 ◽  
Vol 19 (22) ◽  
pp. 14091-14106 ◽  
Author(s):  
Chunshui Lin ◽  
Darius Ceburnis ◽  
Ru-Jin Huang ◽  
Wei Xu ◽  
Teresa Spohn ◽  
...  

Abstract. To gain insight into the spatial and chemical variation in submicron aerosol, a nationwide characterization of wintertime PM1 was performed using an aerosol chemical speciation monitor (ACSM) and aethalometer at four representative sites across Ireland. Dublin, the capital city of Ireland, was the most polluted area with an average PM1 concentration of 8.6 µg m−3, ranging from < 0.5 to 146.8 µg m−3 in December 2016. The PM1 in Dublin was mainly composed of carbonaceous aerosol (organic aerosol (OA) + black carbon (BC)), which, on average, accounted for 80 % of total PM1 mass during the monitoring period. Birr, a small town in the midlands area of Ireland with a population < 1 % of that in Dublin, showed an average PM1 concentration (4.8 µg m−3, ranging from < 0.5 to 63.0 µg m−3 in December 2015) of around half that (56 %) in Dublin. Similarly, the PM1 in Birr was also mainly composed of carbonaceous aerosol, accounting for 77 % of total PM1 mass. OA source apportionment results show that local emissions from residential heating were the dominant contributors (65 %–74 % of the OA) at the two sites, with solid fuel burning, on average, contributing 48 %–50 % of the total OA. On the other hand, Carnsore Point and Mace Head, which are both regional background coastal sites, showed lower average PM1 concentrations (2.2 µg m−3 for Carnsore Point in December 2016 and 0.7 µg m−3 for Mace Head in January 2013) due to the distance from emission sources. Both sites were dominated by secondary aerosol comprising oxygenated OA (OOA), nitrate, sulfate, and ammonium. This nationwide source apportionment study highlights the large contribution of residential solid fuel burning to urban air pollution and identifies specific sources that should be targeted to improve air quality. On the other hand, this study also shows that rural and coastal areas are dominated by secondary aerosol from regional transport, which is more difficult to tackle. Detailed characterization of the spatial and chemical variation in submicron aerosol in this relatively less studied western European region has significant implications for air quality policies and mitigation strategies, as well as for regional-transport aerosol modeling.


2019 ◽  
Author(s):  
Chunshui Lin ◽  
Darius Ceburnis ◽  
Ru-Jin Huang ◽  
Wei Xu ◽  
Teresa Spohn ◽  
...  

Abstract. To get an insight into the spatial and chemical variation of the submicron aerosol, a nationwide characterization of wintertime PM1 was performed using an Aerosol Chemical Speciation Monitor (ACSM) and Aethalometer at four representative sites across Ireland. Dublin, the capital city of Ireland, was the most polluted area with an average PM1 concentration of 8.6 μg m−3, ranging from


2011 ◽  
Vol 11 (4) ◽  
pp. 1603-1619 ◽  
Author(s):  
D. Liu ◽  
J. Allan ◽  
B. Corris ◽  
M. Flynn ◽  
E. Andrews ◽  
...  

Abstract. The experiment presented in this paper was conducted at the Holme Moss site, which is located in the southern Pennines region in Northwestern England during November–December 2006. The strong southwesterly wind during the experimental period, which enhanced the transport of urban pollutants from the conurbations of Greater Manchester and Liverpool, in addition to the seasonally increased nearby residential heating activities, made this site a receptor for pollutants from a range of sources. A factor analysis is applied to the mass spectra of organic matter (OM) measured by the Aerodyne Aerosol Mass Spectrometer (AMS) to attribute the pollutant sources. Besides the oxygenated organic aerosol (OOA), this site was found to contain a considerable fraction of primary organic aerosols (POA, mass fraction 50–70% within total mass of OM). The POA sources are attributed to be traffic emission and solid fuel burning, which are identified as hydrocarbon-like organic aerosol (HOA) and solid fuel organic aerosol (SFOA) respectively. There were strongly combined emissions of black carbon (BC) particles from both sources. The refractory BC component (rBC) was characterized by a single particle soot photometer. This site began to be influenced during the late morning by fresh traffic emissions, whereas solid fuel burning became dominant from late afternoon until night. A covariance analysis of rBC and POA was used to derive source specific emission factors of 1.61 μgHOA/μgrBC and 1.96 μgHOA/μgrBC. The absorbing properties of aerosols were characterized at multiple wavelengths (λ), and a stronger spectral dependence of absorption was observed when this site was significantly influenced by solid fuel burning. The rBC was estimated to contribute 3–16% of submicron aerosol mass. The single scattering albedo at λ = 700 nm (SSA700 nm) was significantly anti-correlated with the rBC mass fraction, but also associated with the BC mixing state. The BC incorporation/removal process therefore may play a role in modulating the radiative properties of aerosols at the site under the influence of fresh sources. Given that traffic and residential combustion of solid fuels are significant contributors of carbonaceous aerosols over Europe, these results provide important source-specific information on modeling the anthropogenic carbonaceous aerosols.


1988 ◽  
Vol 54 (3) ◽  
pp. 296-300 ◽  
Author(s):  
V. A. Munts ◽  
A. P. Baskakov ◽  
A. A. Ashikhmin

2018 ◽  
Vol 52 (4) ◽  
pp. 2385-2391 ◽  
Author(s):  
Hongyun Hu ◽  
Mengya Shi ◽  
Yuhan Yang ◽  
Huan Liu ◽  
Mian Xu ◽  
...  

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