TY - JOUR
T1 - Investigating a two-component model of solid fuel organic aerosol in London: processes, PM1 contributions, and seasonality
AU - Young, Dominique
AU - Allan, J D
AU - Williams, P I
AU - Green, D C
AU - Harrison, R M
AU - Yin, J
AU - Flynn, Michael
AU - Gallagher, Martin
AU - Coe, H
N1 - This work was supported in part by the UK Natural Environment Research Council (NERC) ClearfLo project (grant ref. NE/H008136/1) and is coordinated by the National Centre for Atmospheric Science (NCAS). Additional support for the aerosol measurements was provided by the Department of Environment, Food and Rural Affairs (DEFRA). D. E. Young was supported by a NERC PhD studentship (ref. NE/I528142/1). The authors would like to thank James Lee from NCAS at the University of York for the CO, NO and NO2 data as well as for logistical assistance at the North Kensington supersite during the IOPs. The authors would also like to thank Anja Tremper at King’s College London for assisting with instrument maintenance. Additional thanks to the Sion Manning School in North Kensington and adjacent community centre.Processed data are available through the ClearfLo project archive at the British Atmospheric Data Centre (http://badc. nerc.ac.uk/browse/badc/clearflo). Raw data are archived at the University of Manchester and are available on request.
PY - 2015/3/5
Y1 - 2015/3/5
N2 - Solid fuel emissions, including those from biomass burning, are increasing in urban areas across the European Union due to rising energy costs and government incentives to use renewable energy sources for heating. In order to help protect human health as well as to improve air quality and pollution abatement strategies, the sources of combustion aerosols, their contributions, and the processes they undergo need to be better understood. A high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) was therefore deployed at an urban background site between January and February 2012 to investigate solid fuel organic aerosols (SFOA) in London. The variability of SFOA was examined and the factors governing the split between the two SFOA factors derived from Positive Matrix Factorisation (PMF) were assessed. The concentrations of both factors were found to increase during the night and during cold periods, consistent with domestic space heating activities. The split between the two factors is likely governed predominantly by differences in burn conditions where SFOA1 best represents more efficient burns and SFOA2 best represents less efficient burns. The differences in efficiency may be due to burner types or burn phase, for example. Different fuel types and levels of atmospheric processing also likely contribute to the two factors. As the mass spectral profile of SFOA is highly variable, the findings from this study may have implications for improving future source apportionment and factorisation analyses. During the winter, SFOA was found to contribute 38% to the total non-refractory submicron organic aerosol (OA) mass, with similar contributions from both SFOA factors (20% from SFOA1 and 18% from SFOA2). A similar contribution of SFOA was derived for the same period from a compact time-of-flight AMS (cToF-AMS), which measured for a full calendar year at the same site. The seasonality of SFOA was investigated using the year-long data set where concentrations were greatest in the autumn and winter. During the summer, SFOA contributed 11% to the organic fraction, where emissions resulted from different anthropogenic activities such as barbecues and domestic garden wood burning. The significant contribution of SFOA to total organic mass throughout the year suggests that the negative effects on health and air quality, as well as climate, are not just confined to winter as exposure to these aerosols and the associated black carbon can also occur during the summer, which may have significant implications for air-quality policies and mitigation strategies.
AB - Solid fuel emissions, including those from biomass burning, are increasing in urban areas across the European Union due to rising energy costs and government incentives to use renewable energy sources for heating. In order to help protect human health as well as to improve air quality and pollution abatement strategies, the sources of combustion aerosols, their contributions, and the processes they undergo need to be better understood. A high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) was therefore deployed at an urban background site between January and February 2012 to investigate solid fuel organic aerosols (SFOA) in London. The variability of SFOA was examined and the factors governing the split between the two SFOA factors derived from Positive Matrix Factorisation (PMF) were assessed. The concentrations of both factors were found to increase during the night and during cold periods, consistent with domestic space heating activities. The split between the two factors is likely governed predominantly by differences in burn conditions where SFOA1 best represents more efficient burns and SFOA2 best represents less efficient burns. The differences in efficiency may be due to burner types or burn phase, for example. Different fuel types and levels of atmospheric processing also likely contribute to the two factors. As the mass spectral profile of SFOA is highly variable, the findings from this study may have implications for improving future source apportionment and factorisation analyses. During the winter, SFOA was found to contribute 38% to the total non-refractory submicron organic aerosol (OA) mass, with similar contributions from both SFOA factors (20% from SFOA1 and 18% from SFOA2). A similar contribution of SFOA was derived for the same period from a compact time-of-flight AMS (cToF-AMS), which measured for a full calendar year at the same site. The seasonality of SFOA was investigated using the year-long data set where concentrations were greatest in the autumn and winter. During the summer, SFOA contributed 11% to the organic fraction, where emissions resulted from different anthropogenic activities such as barbecues and domestic garden wood burning. The significant contribution of SFOA to total organic mass throughout the year suggests that the negative effects on health and air quality, as well as climate, are not just confined to winter as exposure to these aerosols and the associated black carbon can also occur during the summer, which may have significant implications for air-quality policies and mitigation strategies.
KW - mass-spectrometer data
KW - residential wood combustion
KW - biomass-burning smoke
KW - source apportionment
KW - high-resolution
KW - air-pollution
KW - particulate matter
KW - urban
KW - time
KW - particles
U2 - 10.5194/acp-15-2429-2015, 2015
DO - 10.5194/acp-15-2429-2015, 2015
M3 - Article
SN - 1680-7316
VL - 15
SP - 2429
EP - 2443
JO - Atmospheric Chemistry and Physics
JF - Atmospheric Chemistry and Physics
IS - 5
ER -