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Climate in the Arctic is changing at a rapid pace. When vegetation reacts to these changes, chemicals called biogenic volatile organic compounds (BVOCs) can be released into the atmosphere in new ways. This project seeks to investigate how climate change affects the quantity and type of BVOCs released into the atmosphere on the North Slope of Alaska (NSA). In addition, we are interested in the chemical reactions these BVOCs undergo in the Arctic atmosphere. Project goals will be accomplished through field work on the NSA, and collection and laboratory analysis of atmospheric samples. Specifically, the project intends to measure the concentration of BVOCs and their secondary organic aerosol products during North Slope of Alaska field campaigns. In addition to BVOCs and organic acids, the measurements include additional baseline measurements of other volatile organic compounds (VOC) and aerosol components. We are reporting inorganic ions, alkanes, and polycyclic aromatic hydrocarbons (PAHs) for aerosol composition and select aromatic and oxidized VOCs. The time period for these detailed measurements is Jun - Aug 2023 for Utqiagvik, Alaska (AK). VOC measurements were made by proton transfer reaction mass spectrometry. The proton transfer reaction mass spectrometer (PTR-MS) was operated with Hydronium (H3O+) ion at the Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) site in Utqiagvik, AK from 170623 to 130823. Total suspended particulate matter samples were collected on quartz fiber filters at a roughly weekly schedule. These filters were then used for offline analysis. Offline measurement of cations and anions was conducted using ion chromatography. Offline measurement of alkanes and PAH was conducted using thermal desorption gas chromatography - mass spectrometry.
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A Novel Method for Carbonate Quantification in Atmospheric Particulate Matter
Inorganic carbonate can be an important component of atmospheric particulate matter in arid environments where mineral dust components contribute significantly to air particulate matter. Carbonate carbon (CC) is only rarely quantified in atmospheric studies and methods to quantify carbonate in atmospheric samples are rare. In this manuscript, we present a novel protocol for quantifying carbonate carbon in atmospheric particulate matter samples, through the acidification of aerosol filters at ambient pressure and temperature and subsequent measurement of carbon dioxide (CO2) released upon acidification. This method is applicable to a variety of filter media used in air pollution studies, such as Teflon, cellulose, or glass fiber filters. The method allows the customization of the filter area used for analysis (up to 24 cm2) so that sufficient CO2 can be detected when released and to assure that the sample aliquot is representative of the whole filter. The resulting detection limits can be as low as 0.12 µg/cm2. The analysis of a known amount of sodium bicarbonate applied to a filter resulted in a relative error within 15% of the known mass of bicarbonate when measured 20 min after acidification. A particulate matter sample with aerodynamic diameter larger than 2.5 µm (PM>2.5) collected via cascade impaction on a high-volume aerosol sampler yielded good precision, with a CC concentration of 4.4 ± 0.3 µgC/cm2 for six replicates. The precision, accuracy, and reproducibility of this method of CC measurement make it a good alternative to existing quantification methods.
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- Award ID(s):
- 1832016
- PAR ID:
- 10200385
- Date Published:
- Journal Name:
- Atmosphere
- Volume:
- 11
- Issue:
- 6
- ISSN:
- 2073-4433
- Page Range / eLocation ID:
- 661
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.3390/atmos11060661
