Use of a gas chromatography–mass spectrometry organic aerosol monitor for in-field detection of fine particulate organic compounds in source apportionment. (4th May 2018)

• Record Type: Journal Article
• Authors: Cropper, Paul M.; Eatough, Delbert J.; Overson, Devon K.; Hansen, Jaron C.; Caka, Fern; Cary, Robert A.
• Is Part Of: Journal of the Air & Waste Management Association. Volume 68:Number 5(2018)
• Page Start: 390
• Page End: 402
• Publication Date: 2018-05-04
• Subjects: Air -- Pollution -- Periodicals; Air quality management -- Periodicals; Hazardous wastes -- Management -- Periodicals; Air Pollution -- prevention & control -- Periodicals; Hazardous Waste -- prevention & control -- Periodicals; Waste Management -- Periodicals; 628.5305
• DOI: 10.1080/10962247.2017.1363095
• Languages: English
• ISSNs: 1047-3289

Abstract

ABSTRACT: A study was conducted on the Brigham Young University campus during January and February 2015 to identify winter-time sources of fine particulate material in Utah Valley, Utah. Fine particulate mass and components and related gas-phase species were all measured on an hourly averaged basis. Light scattering was also measured during the study. Included in the sampling was the first-time source apportionment application of a new monitoring instrument for the measurement of fine particulate organic marker compounds on an hourly averaged basis. Organic marker compounds measured included levoglucosan, dehydroabietic acid, stearic acid, pyrene, and anthracene. A total of 248 hourly averaged data sets were available for a positive matrix factorization (PMF) analysis of sources of both primary and secondary fine particulate material. A total of nine factors were identified. The presence of wood smoke emissions was associated with levoglucosan, dehydroabietic acid, and pyrene markers. Fine particulate secondary nitrate, secondary organic material, and wood smoke accounted for 90% of the fine particulate material. Fine particle light scattering was dominated by sources associated with wood smoke and secondary ammonium nitrate with associated modeled fine particulate water. Implications : The identification of sources and secondary formation pathways leading to observed levels of PM2.5 (particulate matter with an aerodynmaic diameter <2.5 μm) is important in making regulatory decisions on pollution control. The use of organic marker compounds in this assessment has proven useful; however, data obtained on a daily, or longer, sampling schedule limit the value of the information because diurnal changes associated with emissions and secondary aerosol formation cannot be identified. A new instrument, the gas chromtography–mass spectrometry (GC-MS) organic aerosol monitor, allows for the determination on these compounds on an hourly averaged basis. The demonstrated potential value of hourly averaged data in a source apportionment analysis indicates that significant improvement in the data used for making regulatory decisions is possible.