Air quality expert group - Fine particulate matter (PM2.5) in ... - Defra
Air quality expert group - Fine particulate matter (PM2.5) in ... - Defra
Air quality expert group - Fine particulate matter (PM2.5) in ... - Defra
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<strong>PM2.5</strong> emissions and receptor modell<strong>in</strong>g<br />
background site <strong>in</strong> Birm<strong>in</strong>gham. They used a thermal separation of organic<br />
carbon from elemental carbon and were able to determ<strong>in</strong>e the radiocarbon<br />
content of each. By mak<strong>in</strong>g a number of assumptions, they were able to<br />
disaggregate the carbonaceous component of the <strong>PM2.5</strong> <strong>in</strong>to the follow<strong>in</strong>g<br />
components:<br />
• EC biomass, represent<strong>in</strong>g elemental carbon from the burn<strong>in</strong>g of wood and<br />
other contemporary fuels.<br />
• EC fossil, represent<strong>in</strong>g elemental carbon from the combustion of fossil fuels<br />
predom<strong>in</strong>antly <strong>in</strong> diesel eng<strong>in</strong>es but <strong>in</strong>clud<strong>in</strong>g, for example, <strong>in</strong>dustrial oil<br />
and coal combustion.<br />
• OC fossil, represent<strong>in</strong>g organic compounds derived from fossil fuel sources<br />
and hence <strong>in</strong>clud<strong>in</strong>g emissions from road vehicles, but also of solventderived<br />
compounds from <strong>in</strong>dustry and secondary particles derived from<br />
them.<br />
• OC biomass, represent<strong>in</strong>g organic carbon from the combustion of wood<br />
and other biomass fuels.<br />
• OC biogenic, represent<strong>in</strong>g primary organic carbon conta<strong>in</strong>ed, for example,<br />
<strong>in</strong> vegetative detritus, but also secondary organic carbon deriv<strong>in</strong>g from<br />
biogenic precursors.<br />
96. The average composition of the samples analysed by Heal et al. (2011) appears<br />
<strong>in</strong> Figure 4.12 where it is compared with data from Zurich, Switzerland, and<br />
Göteborg, Sweden. In Table 4.7, the masses of organic carbon reported for<br />
the Birm<strong>in</strong>gham sites have been converted to approximate masses of organic<br />
<strong>matter</strong>, so as to give a breakdown of the carbonaceous aerosol based upon<br />
the average concentration (over 26 samples) of total carbon of 5.00 µg m -3 <strong>in</strong><br />
the <strong>PM2.5</strong> fraction. The rather low percentage attributable to the burn<strong>in</strong>g of<br />
wood and other biomass tends to confirm the low contributions seen <strong>in</strong> the<br />
results of Y<strong>in</strong> et al. (2010), but perhaps the most strik<strong>in</strong>g f<strong>in</strong>d<strong>in</strong>g is the high<br />
percentage attributable to biogenic organic carbon. Given the relatively modest<br />
contribution of vegetative detritus shown by Y<strong>in</strong> et al. (2010) and seen <strong>in</strong> Figure<br />
4.10, this is most probably largely secondary organic carbon, and it appears that<br />
secondary organic <strong>matter</strong> (OM) from biogenic precursors makes a much larger<br />
contribution to the overall total OM than secondary organic carbon from fossil<br />
fuel precursors.<br />
97. The work by Heal et al. (2011) to dist<strong>in</strong>guish contemporary from fossil carbon<br />
suggests that a large proportion of secondary organic carbon is biogenic <strong>in</strong><br />
orig<strong>in</strong> (Table 4.7) and hence unlikely to decrease significantly <strong>in</strong> concentration <strong>in</strong><br />
the foreseeable future as it is unlikely to be subject to control measures.<br />
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