The Global Threat from the Irreversible Accumulation of Trifluoroacetic Acid (TFA)
- PMID: 39475534
- PMCID: PMC11562725
- DOI: 10.1021/acs.est.4c06189
The Global Threat from the Irreversible Accumulation of Trifluoroacetic Acid (TFA)
Abstract
Trifluoroacetic acid (TFA) is a persistent and mobile substance that has been increasing in concentration within diverse environmental media, including rain, soils, human serum, plants, plant-based foods, and drinking water. Currently, TFA concentrations are orders of magnitude higher than those of other per- and polyfluoroalkyl substances (PFAS). This accumulation is due to many PFAS having TFA as a transformation product, including several fluorinated gases (F-gases), pesticides, pharmaceuticals, and industrial chemicals, in addition to direct release of industrially produced TFA. Due to TFA's extreme persistence and ongoing emissions, concentrations are increasing irreversibly. What remains less clear are the thresholds where irreversible effects on local or global scales occur. There are indications from mammalian toxicity studies that TFA is toxic to reproduction and that it exhibits liver toxicity. Ecotoxicity data are scarce, with most data being for aquatic systems; fewer data are available for terrestrial plants, where TFA bioaccumulates most readily. Collectively, these trends imply that TFA meets the criteria of a planetary boundary threat for novel entities because of increasing planetary-scale exposure, where potential irreversible disruptive impacts on vital earth system processes could occur. The rational response to this is to instigate binding actions to reduce the emissions of TFA and its many precursors.
Keywords: PFAS; PMT; environmental monitoring; multigenerational exposure; trifluoroacetic acid; vPvM.
Conflict of interest statement
The authors declare no competing financial interest.
Figures
References
-
- Janda J.; Nödler K.; Brauch H. J.; Zwiener C.; Lange F. T. Robust Trace Analysis of Polar (C2-C8) Perfluorinated Carboxylic Acids by Liquid Chromatography-Tandem Mass Spectrometry: Method Development and Application to Surface Water, Groundwater and Drinking Water. Environmental Science and Pollution Research 2019, 26 (8), 7326–7336. 10.1007/s11356-018-1731-x. - DOI - PubMed
-
- Neuwald I. J.; Hübner D.; Wiegand H. L.; Valkov V.; Borchers U.; Nödler K.; Scheurer M.; Hale S. E.; Arp H. P. H.; Zahn D. Ultra-Short-Chain PFASs in the Sources of German Drinking Water: Prevalent, Overlooked, Difficult to Remove, and Unregulated. Environ. Sci. Technol. 2022, 56, 6380. 10.1021/acs.est.1c07949. - DOI - PubMed
-
- Liang S. H.; Steimling J. A.; Chang M. Analysis of Ultrashort-Chain and Short-Chain (C1 to C4) per- and Polyfluorinated Substances in Potable and Non-Potable Waters. Journal of Chromatography Open 2023, 4, 100098. 10.1016/j.jcoa.2023.100098. - DOI
-
- Tian Y.; Yao Y.; Chang S.; Zhao Z.; Zhao Y.; Yuan X.; Wu F.; Sun H. Occurrence and Phase Distribution of Neutral and Ionizable Per- and Polyfluoroalkyl Substances (PFASs) in the Atmosphere and Plant Leaves around Landfills: A Case Study in Tianjin, China. Environ. Sci. Technol. 2018, 52 (3), 1301–1310. 10.1021/acs.est.7b05385. - DOI - PubMed
-
- Chen H.; Yao Y.; Zhao Z.; Wang Y.; Wang Q.; Ren C.; Wang B.; Sun H.; Alder A. C.; Kannan K. Multimedia Distribution and Transfer of Per- and Polyfluoroalkyl Substances (PFASs) Surrounding Two Fluorochemical Manufacturing Facilities in Fuxin, China. Environ. Sci. Technol. 2018, 52 (15), 8263–8271. 10.1021/acs.est.8b00544. - DOI - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
