Growth in Production and Environmental Deposition of Trifluoroacetic Acid Due To Long‐Lived CFC Replacements and Anesthetics

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Authors: Lucy Hart, Ryan Hossaini, Oliver Wild, Andrea Mazzeo, Crispin Halsall, Xuewei Hou, Zihao Wang, Martyn P. Chipperfield, Jgor Arduini, Paul B. Krummel, Chris R. Lunder, Jens JMühle
+6 more Simon O’Doherty, 박선영, Stefan Reimann, Kieran Stanley, R. F. Weiss, Dickon Young
Cited by: 3
References: 56

Abstract

Abstract Trifluoroacetic acid (TFA) is a persistent pollutant with potential long‐term effects on the environment and on health. Recent studies using ice core records report large increases (up to tenfold) in Arctic TFA deposition since the 1970s, and trends suggest long‐lived chlorofluorocarbon (CFC) replacements may be a major source. Here, we use a chemical transport model to examine the global TFA budget arising from CFC replacements–hydrochlorofluorocarbons (HCFCs), hydrofluorocarbons (HFCs)–and inhalation anesthetics. Global TFA deposition from these sources increased ∼3.5‐fold from 6.8 (5.9–7.6) Gg/yr in 2000 to 21.8 (18.6–25.0) Gg/yr in 2022, with cumulative deposition reaching 335.5 Gg. We find HCFC‐123, HCFC‐124, and HFC‐134a account for most modeled TFA production and that long‐lived CFC replacements account for virtually all of the observed Arctic deposition trend. At lower latitudes, our analysis supports the recent emergence of hydrofluoroolefins (HFOs) as a TFA source. We conclude that increased TFA monitoring is required.

Fields of Study & Subjects

Per- and polyfluoroalkyl substances research Atmospheric Ozone and Climate Fluoride Effects and Removal

Publication details

Journal / source
Geophysical Research Letters
Publisher
American Geophysical Union (AGU)
Volume
53
Issue
3
Publication date
4 February 2026
Language
EN