Comparison of Real-Time and Offline Mass Spectrometry Methods for Quantitation of Fluorotelomer Alcohols in Aqueous
Gabrielle V West1,2, Kenneth S Docherty1, Matthew S Clifton3
1Center for Environmental Measurement and Modeling, Air Methods and Characterization Division, U.S. EPA, 109 T.W. Alexander Drive, Research Triangle Park, North Carolina27711, United States.
Abstract:
Per- and polyfluoroalkyl substances (PFAS) are highly water-, grease-, and heat-resistant compounds known as "forever chemicals" due to their resistance to degradation. Aqueous film-forming foams (AFFFs) are PFAS-containing firefighting foams and a known source of environmental PFAS contamination. Recent research characterizing PFAS contamination at historical AFFF usage sites has advanced our understanding of environmental fate and transport of water-soluble PFAS. However, emissions of volatile or semivolatile PFAS from AFFFs during their storage and application and from AFFF-contaminated sites remain largely uncharacterized, in part due to analytical method limitations. This work quantified fluorotelomer alcohols (FTOHs) in the headspace above three AFFF formulations using two emerging analytical techniques: thermal desorption-gas chromatography/mass spectrometry (TD-GC/MS) and real-time iodide chemical ionization mass spectrometry (I-CIMS). Thermal desorption tube samples were collected for offline analysis via TD-GC/MS, while I-CIMS simultaneously sampled the headspace. Then, the FTOH headspace concentrations quantified by the two techniques were compared. In all three formulations, 6:2 and 8:2 FTOHs were the most and second-most abundant, respectively. The FTOH concentrations quantified by TD-GC/MS ranged from 0.06 to 2.0 μg/m3, while those quantified by I-CIMS ranged from 0.13 to 4.4 μg/m3. The percent error between the two methods ranged from 10 to 102%. These results underscore the need for additional research exploring the factors that impact the quantitative accuracy of both methods.
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