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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 />

117

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