TY - JOUR
T1 - Major source categories for PM2.5 in Pittsburgh using PMF and UNMIX
AU - Pekney, Natalie
AU - Davidson, Cliff
AU - Robinson, Allen
AU - Zhou, Liming
AU - Hopke, Philip
AU - Eatough, Delbert
AU - Rogge, Wolfgang
N1 - Funding Information:
This research was conducted as a part of the Pittsburgh Air Quality Study which was supported by the US Environmental Protection Agency under contract R82806101 and the US Department of Energy National Energy Technology Laboratory under contract DE-FC26-01NT41017. This paper has not been subject to EPA’s peer and policy review, and therefore does not necessarily reflect the views of the Agency. No official endorsement should be inferred.
PY - 2006/10/1
Y1 - 2006/10/1
N2 - An objective of the Pittsburgh Air Quality Study was to determine the major sources of PM2.5 in the Pittsburgh region. Daily 24-hour averaged filter-based data were collected for 13 months, starting in July 2001, including sulfate and nitrate data from IC analysis, trace element data from ICP-MS analysis, and organic and elemental carbon from the thermal optical transmittance (TOT) method and the NIOSH thermal evolution protocol. These data were used in two source-receptor models, Unmix and PMF. Unmix, which is limited to a maximum number of seven factors, resolved six source factors, including crustal material, a regional transport factor, secondary nitrate, an iron, zinc and manganese factor, specialty steel production and processing, and cadmium. PMF, which has no limit to the number of factors, apportioned the PM 2.5 mass into ten factors, including crustal material, secondary sulfate, primary OC and EC, secondary nitrate, an iron, zinc and manganese factor, specialty steel production and processing, cadmium, selenium, lead, and a gallium-rich factor. The Unmix and PMF common factors agree reasonably well, both in composition and contributions to PM2.5. To further identify and apportion the sources of PM2.5, specific OC compounds that are known markers of some sources were added to the PMF analysis. The results were similar to the original solution, except that the primary OC and EC factor split into two factors. One factor was associated with vehicles as identified by the hopanes, PAH's, and other OC compounds. The other factor had strong correlations with the OC and EC ambient data as well as wood smoke markers such as levoglucosan, syringols, and resin acids.
AB - An objective of the Pittsburgh Air Quality Study was to determine the major sources of PM2.5 in the Pittsburgh region. Daily 24-hour averaged filter-based data were collected for 13 months, starting in July 2001, including sulfate and nitrate data from IC analysis, trace element data from ICP-MS analysis, and organic and elemental carbon from the thermal optical transmittance (TOT) method and the NIOSH thermal evolution protocol. These data were used in two source-receptor models, Unmix and PMF. Unmix, which is limited to a maximum number of seven factors, resolved six source factors, including crustal material, a regional transport factor, secondary nitrate, an iron, zinc and manganese factor, specialty steel production and processing, and cadmium. PMF, which has no limit to the number of factors, apportioned the PM 2.5 mass into ten factors, including crustal material, secondary sulfate, primary OC and EC, secondary nitrate, an iron, zinc and manganese factor, specialty steel production and processing, cadmium, selenium, lead, and a gallium-rich factor. The Unmix and PMF common factors agree reasonably well, both in composition and contributions to PM2.5. To further identify and apportion the sources of PM2.5, specific OC compounds that are known markers of some sources were added to the PMF analysis. The results were similar to the original solution, except that the primary OC and EC factor split into two factors. One factor was associated with vehicles as identified by the hopanes, PAH's, and other OC compounds. The other factor had strong correlations with the OC and EC ambient data as well as wood smoke markers such as levoglucosan, syringols, and resin acids.
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U2 - 10.1080/02786820500380271
DO - 10.1080/02786820500380271
M3 - Article
AN - SCOPUS:33745830172
SN - 0278-6826
VL - 40
SP - 910
EP - 924
JO - Aerosol Science and Technology
JF - Aerosol Science and Technology
IS - 10
ER -