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Organic molecular tracers, also referred to as organic molecular markers, are compounds or compound classes of interest in the field of air quality because they can help identify particulate emission sources, as they are relatively unique to those sources. This approach is generally applied to particulate matter under 2.5μm in diameter because of the formation mechanisms and the health risks associated with this size regime^[1]. With tracer compounds,the principles of mass balance are used to 'trace' emissions from the source to the receptor site where a sample is taken. Organic compounds have gained popularity as tracers as analysis costs have decreased, the quality of the measurements has improved, and species that were historically good tracers, such as lead, have decreased in ambient concentrations due to various factors including government regulation.

Requirements for Organic Molecular Tracers

In order to be used as a tracer, a compound must be emitted preferentially by some sources and not by others, giving the emission source a relatively unique chemical makeup. The compound must react slowly enough in the atmosphere that it is chemically conserved from the emission source to the receptor site where an ambient sample may be taken. Additionally, a tracer species should not be formed in the atmosphere and it should not volatilize during transport, in order to maintain a mass balance.^[2]. Tracer compounds must then be of primary origins, which are created through condensation and coagulation of mainly combustion and biological sources^[3].

Example of Organic Molecular Tracers

Samples have been analyzed from many known biogenic and anthropogenic emissions sources such as diesel and gasoline vehicles, cigarette smoke, road dust, vegetative detritus, wood smoke, and meat cooking. Examples of some results of preferential emissions from sources include hopanes, polycyclic aromatic hydrocarbons and steranes ^[4] from different types of mobile sources, retene and methoxyphenols from wood smoke, odd n-alkanes and even n-alkanoic acids from vegetative detritus, cholesterol and the C16 and C18 n-alkanoic acids from cooking, and lighter n-alkanes from brake wear.^[5]

Analysis using Organic Molecular Markers

Chemical analysis of ambient and source samples is performed using gas chromatography-mass spectrometry, and the chemical profile of the emission sources can be compared to an ambient sample using chemical mass balance techniques to identify the ambient mass contribution from each pollution source. This approach assumes that an ambient air sample has particulate matter contributions from a linear combination of emission sources. If the chemical compositions of local sources are not available, source apportionment models such as Positive Matrix Factorization and principal components analysis can be used by employing statistical methods to identify emissions sources from time series of ambient samples.

References

^ Pope Ca, 3rd; Burnett, R. T.; Thun, M. J.; Calle, E. E.; Krewski, D.; Ito, K.; Thurston, G. D. (2002). "Cancer, cardiopulmonary mortality, and long-term exposure to fine particulate air pollution". J. Amer. Med. Assoc. 287 (9): 1132–1141. doi:10.1001/jama.287.9.1132. PMC 4037163. PMID 11879110.{{cite journal}}: CS1 maint: numeric names: authors list (link)
^ Cass, Glen R (1998). "Organic molecular tracers for particulate air pollution sources". TrAC Trends in Analytical Chemistry. 17 (6): 356–366. doi:10.1016/S0165-9936(98)00040-5.
^ H Seinfeld and N. Pandis. Atmospheric chemistry and physics: from air pollution to climate change‎. (2006)
^ Rogge, Wolfgang F. (1993). "Sources of fine organic aerosol 1-9". Environmental Science and Technology. 27 (13): 2700–2711. doi:10.1021/es00049a008. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
^ Schauer, James J. (1999). "Measurement of Emissions from Air Pollution Sources. 1-5". Environmental Science and Technology. 36 (6): 1169–1180. doi:10.1021/es0108077. PMID 11944666. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)

External links

EPA-Chemical Mass Balance 8.2

[pope-1] Pope Ca, 3rd; Burnett, R. T.; Thun, M. J.; Calle, E. E.; Krewski, D.; Ito, K.; Thurston, G. D. (2002). "Cancer, cardiopulmonary mortality, and long-term exposure to fine particulate air pollution". J. Amer. Med. Assoc. 287 (9): 1132–1141. doi:10.1001/jama.287.9.1132. PMC 4037163. PMID 11879110.{{cite journal}}: CS1 maint: numeric names: authors list (link)

[cass-2] Cass, Glen R (1998). "Organic molecular tracers for particulate air pollution sources". TrAC Trends in Analytical Chemistry. 17 (6): 356–366. doi:10.1016/S0165-9936(98)00040-5.

[3] H Seinfeld and N. Pandis. Atmospheric chemistry and physics: from air pollution to climate change‎. (2006)

[Rogge-4] Rogge, Wolfgang F. (1993). "Sources of fine organic aerosol 1-9". Environmental Science and Technology. 27 (13): 2700–2711. doi:10.1021/es00049a008. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)

[Schauer-5] Schauer, James J. (1999). "Measurement of Emissions from Air Pollution Sources. 1-5". Environmental Science and Technology. 36 (6): 1169–1180. doi:10.1021/es0108077. PMID 11944666. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)

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