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
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
<strong>PM2.5</strong> emissions and receptor modell<strong>in</strong>g<br />
4.6.2 Comparison of receptor modell<strong>in</strong>g results with output from<br />
the PCM model<br />
90. Both receptor modell<strong>in</strong>g methods and the PCM model <strong>in</strong>evitably have<br />
weaknesses and uncerta<strong>in</strong>ties associated with their outputs. The chemical<br />
mass balance approach to source apportionment is limited to quantify<strong>in</strong>g<br />
those sources for which source chemical profiles are available as <strong>in</strong>puts and<br />
consequently this may miss many m<strong>in</strong>or sources. Additionally, the source<br />
chemical profile <strong>in</strong>formation is derived <strong>in</strong> the ma<strong>in</strong> from US studies which<br />
may not be wholly applicable to the UK situation. One example is that of road<br />
vehicle emissions, for which Y<strong>in</strong> et al. (2010) highlight differences <strong>in</strong> the vehicle<br />
parc between the fleet at the time of sampl<strong>in</strong>g and the vehicles used <strong>in</strong> the<br />
key North American study which characterised the source emissions profiles.<br />
This <strong>in</strong>evitably adds uncerta<strong>in</strong>ties to the assignments. In the case of PCM,<br />
those components estimated by dispersion modell<strong>in</strong>g are only as good as the<br />
source emissions <strong>in</strong>ventories, which for some sources are subject to very large<br />
uncerta<strong>in</strong>ties aris<strong>in</strong>g from the difficulties <strong>in</strong> collect<strong>in</strong>g suitable data.<br />
91. Comparison of the two approaches to source apportionment is made especially<br />
difficult by the fact that the source categories <strong>in</strong> the two models do not map<br />
directly onto one another. However, by mak<strong>in</strong>g certa<strong>in</strong> assumptions, it is possible<br />
to compare generic categories. The other key reservation <strong>in</strong> compar<strong>in</strong>g the two<br />
modell<strong>in</strong>g approaches is that data are not available for the same time periods.<br />
The Y<strong>in</strong> et al. (2010) study <strong>in</strong>volved aerosol sampl<strong>in</strong>g over a 12-month period<br />
from May 2007 to April 2008. Daily <strong>PM2.5</strong> samples were collected for five<br />
days (Monday to Friday) at the beg<strong>in</strong>n<strong>in</strong>g of each month us<strong>in</strong>g two co-located<br />
samplers at each site. Consequently, the results, although cover<strong>in</strong>g a 12-month<br />
period, represent the analysis of only 60 weekday samples. On the other hand,<br />
results from the PCM represent the analysis of annual means for the year 2009.<br />
A comparison of the outputs of the two approaches appears <strong>in</strong> Table 4.6 and<br />
Figure 4.11. In order to make this comparison, source categories disaggregated<br />
by the PCM have had to be comb<strong>in</strong>ed <strong>in</strong> order to map onto the sources identified<br />
by the chemical mass balance receptor model, and <strong>in</strong> some cases categories<br />
identified by the receptor model have had to be comb<strong>in</strong>ed <strong>in</strong> order to match the<br />
PCM outputs. The assumptions made are listed <strong>in</strong> the notes to Table 4.6.<br />
92. View<strong>in</strong>g Table 4.6 and Figure 4.11, the most obvious difference is <strong>in</strong> the<br />
secondary <strong>in</strong>organic fraction and this can be expla<strong>in</strong>ed by the use of different<br />
sampl<strong>in</strong>g periods. The traffic and off-road/smok<strong>in</strong>g eng<strong>in</strong>e categories are<br />
broadly similar for the two models, especially when view<strong>in</strong>g the sum of the two<br />
categories, given that the CMB model probably does not adequately dist<strong>in</strong>guish<br />
off-road emissions from malfunction<strong>in</strong>g on-road vehicles. By far the largest<br />
divergence between the models is <strong>in</strong> the category of <strong>in</strong>dustry/commercial/<br />
domestic emissions (14% of total emissions <strong>in</strong> the PCM and 2% <strong>in</strong> the CMB).<br />
This category (see note to Table 4.6) <strong>in</strong> the case of the PCM comprises the<br />
sum of <strong>in</strong>dustry, commercial and domestic categories and half of the longrange<br />
transported primary <strong>particulate</strong> <strong>matter</strong>, while for the CMB model it is<br />
the sum of natural gas, coal and wood combustion aerosol. S<strong>in</strong>ce a substantial<br />
proportion of the <strong>in</strong>dustrial, commercial and domestic categories <strong>in</strong> the PCM<br />
model comprises particles from the combustion of natural gas and coal, there is<br />
a very real divergence. It appears that the NAEI uses a very high emission factor<br />
for emissions from natural gas combustion. However, the PCM also <strong>in</strong>cludes<br />
113