Health Assessment Document for Diesel Emissions - NSCEP | US ...
Health Assessment Document for Diesel Emissions - NSCEP | US ...
Health Assessment Document for Diesel Emissions - NSCEP | US ...
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1 sample collection. There was no breakdown of traffic into numbers of diesel- and gasoline-<br />
2 fueled vehicles.<br />
3 The range of particle-phase P AH concentrations and the mean particle- and vapor-phase<br />
4 PAH concentrations <strong>for</strong> 48 samples collected in the tunnel are tabulated in Table 2-16. The<br />
5 ratios of mean particle-phase PAH concentrations to that ofB[e]P, which is considered to be a<br />
6 nonreactive PAH, are also given in this table.<br />
7 As can be seen from Table 2-l6, alkyl-substituted phenanthrenes in the tunnel samples<br />
8 had relatively high concentrations compared with those of the parent compound. This suggests a<br />
9 significant contribution from diesel vehicle emissions (particularly diesel-fueled trucks) because<br />
1 0 extracts of diesel particulate matter are known to have significant concentrations of methyl and<br />
11 dimethylphenanthrenes (see Table 2-8 and Yu and Hites, 1981).<br />
12 Factor analysis was applied to the tunnel data in an attemptto identify factors associated<br />
13 with different types of vehicles; two factors were obtained. The alkylated phenanthrenes loaded<br />
14 significantly on factor 1, suggesting the diesel vehicles as the source of these compounds.<br />
15 Several of the higher-molecular-weight P AHs loaded onto factor 2, which may be associated<br />
16 with the contribution of gasoline-fueled emissions in the tunnel.<br />
17 Ambient air sampling <strong>for</strong> P AHs was also conducted during a summertime photochemical<br />
18 air pollution episode in Glendora, CA, at· a site situated less than 1 km froin the heavily traveled<br />
19 I-210 freeway and generally downwind ofLos Angeles; there<strong>for</strong>e, the site was affected by motor<br />
20 vehicle emissions (Atkinson et al., 1988). Samples were collected by means ofhigh-volume<br />
21 samplers equipped with Teflon-impregnated glass-fiber filters backed by PUF plugs. Table 2-17<br />
22 shows the average (from three daytime and three nighttime samples) concentrations of P AH<br />
23 measured and the ratios of these concentrations to that ofB[e ]P. Un<strong>for</strong>tunately, no alkylated<br />
24 phenanthrenes were measured.<br />
25 As can be seen from the comparison of Tables 2-16 and 2-17, the concentrations of all<br />
26 P AHs measured in Glendora were much lower than those measured in the tunnel, as would be<br />
27 expected. However, the ratios of the concentrations of particle-bound PAH to those ofB[e]P<br />
28 were also different <strong>for</strong> the two sites, usually much lower <strong>for</strong> the Glendora site (except <strong>for</strong> higher<br />
29 molecular weight PAHs, indeno[1,2,3-cd]pyrene, benzo[ghi]perylene, and coronene). This may<br />
30 indicate either contributions from sources other than motor vehicles in the Glendora study or<br />
31 P AH photochemical trans<strong>for</strong>mations occurring on particles prior to or during high-volume<br />
32 sample collections (or both). The generally higher P AH concentrations <strong>for</strong> nighttime versus<br />
33 daytime sampling periods (Atkinson et al., 1988) seem to support the latter possibility. However,<br />
34 the influence of meteorology cannot be excluded. This conclusion is also consistent with high<br />
35 levels of photochemical pollutants observed in Glendora; <strong>for</strong> example, the daily maxima of 0 3<br />
2/1/98 2-49 DRAFT --DO NOT CITE OR QUOTE