Journal
ENVIRONMENTAL SCIENCE & TECHNOLOGY LETTERS
Volume 7, Issue 5, Pages 343-350Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.estlett.0c00114
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Funding
- Early Career Award from the U.S. Environmental Protection Agency Science to Achieve Results (STAR) Program [RD83966]
- NIH [5P30GM103329-05]
- University of North Dakota Pilot Postdoctoral Program from the Office of Vice President for Research & Economic Development
- Larson Foundation
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The aims of this study were two-fold: (1) to improve our understanding of the thermal stability of per- and polyfluoroalkyl substances and (2) to investigate their decomposition mechanisms on spent granular activated carbon (GAC) during thermal reactivation. We studied seven perfluoroalkyl carboxylic acids (PFCAs), three perfluoroalkyl sulfonic acids (PFSAs), and one perfluoroalkyl ether carboxylic acid (PFECA) in different atmospheres (N-2, O-2, CO2, and air). The destabilization of studied compounds during thermal treatment followed first-order kinetics. The temperature needed for thermally destabilizing PFCAs increased with the number of perfluorinated carbons (n(CF2)). Decomposition of PFCAs such as perfluorooctanoic acid (PFOA) on GAC initiated at temperatures as low as 200 degrees C. The PFECA was even more readily decomposed than PFCA with the same n(CF2). PFSAs such as perfluorooctanesulfonic acid (PFOS), on the other hand, required a much higher temperature (>= 450 degrees C) to decompose. Volatile organofluorine species were the main thermal decomposition product of PFOA and PFOS at low to moderate temperatures (<= 600 degrees C). Efficient mineralization to fluoride ions (>80%) of PFOA and PFOS on GAC occurred at 700 degrees C or higher, accompanied by near complete PFOA and PFOS decomposition (>99.9%). Thermal decomposition pathways of PFOA were proposed.
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