PM2.5 pollution from household solid fuel burning practices in Central India: 2. Application of receptor models for source apportionment

2016 ◽  
Vol 40 (1) ◽  
pp. 145-161 ◽  
Author(s):  
Jeevan Lal Matawle ◽  
Shamsh Pervez ◽  
Manas Kanti Deb ◽  
Anjali Shrivastava ◽  
Suresh Tiwari
Keyword(s):  
Source Apportionment ◽  
Solid Fuel ◽  
Central India ◽  
Receptor Models ◽  
Fuel Burning

scholarly journals Wintertime aerosol dominated by solid-fuel-burning emissions across Ireland: insight into the spatial and chemical variation in submicron aerosol

2019 ◽  
Vol 19 (22) ◽  
pp. 14091-14106 ◽  
Author(s):  
Chunshui Lin ◽  
Darius Ceburnis ◽  
Ru-Jin Huang ◽  
Wei Xu ◽  
Teresa Spohn ◽  
...  
Keyword(s):  
Air Quality ◽  
Source Apportionment ◽  
Solid Fuel ◽  
The Other ◽  
Carbonaceous Aerosol ◽  
Chemical Variation ◽  
Submicron Aerosol ◽  
Fuel Burning ◽  
Insight Into

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.

PM2.5 pollution from household solid fuel burning practices in central India: 1. Impact on indoor air quality and associated health risks

2016 ◽  
Vol 39 (5) ◽  
pp. 1045-1058 ◽  
Author(s):  
Jeevan Lal Matawle ◽  
Shamsh Pervez ◽  
Anjali Shrivastava ◽  
Suresh Tiwari ◽  
Pallavi Pant ◽  
...  
Keyword(s):  
Air Quality ◽  
Indoor Air Quality ◽  
Health Risks ◽  
Indoor Air ◽  
Solid Fuel ◽  
Central India ◽  
Fuel Burning

scholarly journals On the use of reference mass spectra for reducing uncertainty in source apportionment of solid-fuel burning in ambient organic aerosol

2021 ◽  
Vol 14 (10) ◽  
pp. 6905-6916
Author(s):  
Chunshui Lin ◽  
Darius Ceburnis ◽  
Anna Trubetskaya ◽  
Wei Xu ◽  
William Smith ◽  
...  
Keyword(s):  
Source Apportionment ◽  
Solid Fuel ◽  
Mass Spectra ◽  
Organic Aerosol ◽  
Solid Fuels ◽  
Winter Period ◽  
Aerosol Mass ◽  
Eu Directive ◽  
A Value ◽  
Fuel Burning

Abstract. Reference mass spectra are routinely used to facilitate source apportionment of ambient organic aerosol (OA) measured by aerosol mass spectrometers. However, source apportionment of solid-fuel-burning emissions can be complicated by the use of different fuels, stoves, and burning conditions. In this study, the organic aerosol mass spectra produced from burning a range of solid fuels in several heating stoves have been compared using an aerosol chemical speciation monitor (ACSM). The same samples of biomass briquettes and smokeless coal were burnt in a conventional stove and Ecodesign stove (Ecodesign refers to a stove conforming to EU Directive 2009/125/EC), while different batches of wood, peat, and smoky coal were also burnt in the conventional stove, and the OA mass spectra were compared to those previously obtained using a boiler stove. The results show that although certain ions (e.g., m/z 60) remain important markers for solid-fuel burning, the peak intensities obtained at specific m/z values in the normalized mass spectra were not constant with variations ranging from < 5 % to > 100 %. Using the OA mass spectra of peat, wood, and coal as anchoring profiles and the variation of individual m/z values for the upper/lower limits (the limits approach) in the positive matrix factorization (PMF) analysis with the Multilinear Engine algorithm (ME-2), the respective contributions of these fuels to ambient submicron aerosols during a winter period in Dublin, Ireland, were evaluated and compared with the conventional a-value approach. The ME-2 solution was stable for the limits approach with uncertainties in the range of 2 %–7 %, while relatively large uncertainties (8 %–29 %) were found for the a-value approach. Nevertheless, both approaches showed good agreement overall, with the burning of peat (39 % vs. 41 %) and wood (14 % vs. 11 %) accounting for the majority of ambient organic aerosol during polluted evenings, despite their small uses compared to electricity and gas. This study, thus, accounts for the source variability in ME-2 modelling and provides better constraints on the primary factor contributions to the ambient organic aerosol estimations. The finding from this study has significant implications for public health and policymakers considering that it is often the case that different batches of solid fuels are often burnt in different stoves in real-world applications.

scholarly journals On the use of reference mass spectra for reducing uncertainty in source apportionment of solid fuel burning in ambient organic aerosol

2021 ◽  
Author(s):  
Chunshui Lin ◽  
Darius Ceburnis ◽  
Anna Trubetskaya ◽  
Wei Xu ◽  
William Smith ◽  
...  
Keyword(s):  
Source Apportionment ◽  
Solid Fuel ◽  
Mass Spectra ◽  
Organic Aerosol ◽  
Solid Fuels ◽  
Winter Period ◽  
Aerosol Mass ◽  
A Value ◽  
Fuel Burning ◽  
Smoky Coal

Abstract. Reference mass spectra are routinely used to facilitate source apportionment of ambient organic aerosol (OA) measured by an aerosol chemical speciation monitor (ACSM). However. source apportionment of solid fuel burning emissions can be complicated by the use of different fuels, stoves and burning conditions. In this study, the organic aerosol mass spectra produced from burning a range of solid fuels in several stoves have been compared using an ACSM. The same samples of biomass briquettes and smokeless coal were burnt in a conventional and Ecodesign stove, while different batches of wood, peat, and smoky coal were also burnt in the conventional stove and the OA mass spectra compared to those previously obtained using a boiler stove. The results shows that although certain ions (e.g., m/z 60) remain important markers for solid fuel burning, the peak intensities obtained at specific m/z values were not constant with variations ranging from <5% to >100 %. Using the OA mass spectra of peat, wood and coal as anchoring profiles and the variation of individual m/z values for the upper/lower limits in ME-2 analysis (the limits approach), the respective contributions of these fuels to ambient sub-micron aerosols during a winter period in Dublin were evaluated and compared with the conventional a value approach. The ME-2 solution was stable for the limits approach with uncertainties in the range of 2–7 %, while relatively large uncertainties (8–29 %) were found for the a value approach. Nevertheless, both approaches showed good agreement overall, with the burning of peat (39 % vs 41 %) and wood (14 % vs 11 %) accounting for the majority of ambient organic aerosol during polluted evenings, despite their small uses. This study, thus, accounts for the source variability in ME-2 modelling and provides better constraints on the primary factor contributions to the ambient organic aerosol estimations. The finding from this study has significant implications for public health and policymakers considering that it is often the case that different batches of solid fuels are often burned in different stoves in real-world applications.

scholarly journals Carbonaceous aerosols contributed by traffic and solid fuel burning at a polluted rural site in Northwestern England

2011 ◽  
Vol 11 (4) ◽  
pp. 1603-1619 ◽  
Author(s):  
D. Liu ◽  
J. Allan ◽  
B. Corris ◽  
M. Flynn ◽  
E. Andrews ◽  
...  
Keyword(s):  
Solid Fuel ◽  
Mass Fraction ◽  
Organic Aerosol ◽  
Radiative Properties ◽  
Rural Site ◽  
Specific Information ◽  
Carbonaceous Aerosols ◽  
Traffic Emission ◽  
Aerosol Mass ◽  
Fuel Burning

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.

Sign in / Sign up

Export Citation Format

Share Document