The influence of functional groups on the pyrolysis of per- and polyfluoroalkyl substances

Abstract

Thermal treatment is a widely used remediation strategy for PFAS-contaminated materials such as soil, spent sorbents, and domestic waste. To better understand the effectiveness and environmental impact of thermal treatments for PFAS-contaminated materials, a fundamental understanding of PFAS thermal degradation mechanisms is required. This work aims to study the pyrolysis of six representative PFAS compounds, all of which have an eight-carbon length but with different functional groups. To assess the thermal stability and pyrolysis products of these six PFAS compounds, evolved gas analysis (EGA) was performed using thermogravimetric analysis/differential scanning calorimetry (TGA/DSC) coupled with an infrared spectrometer (IR) and a mass spectrometer (MS), as well as pyrolysis-GCMS (Pyr-GCMS). The EGA data demonstrates that compounds with lower estimated vapor pressures were generally found to be more thermally labile, and the presence of an ionic bond necessitates higher temperatures for pyrolysis. Pyrolysis at 900 °C yielded a variety of fluorinated organic compounds at significant signals. Tetrafluoroethene constituted the majority of the Pyr-GCMS signal for all the compounds. Moreover, a significant fraction of detected products was unable to be identified, underscoring a need for better tools to help with the identification of unknowns. Pyrolysis can occur through random chain scission, scission of the functional group, scission of the terminal CF₃ group, and HF elimination. Some compounds may undergo more complete beta-scission to produce smaller pyrolysis products compared to others. The presence of acidic protons within the functional group can help facilitate HF elimination, whereas the salt form of a PFAS compound is less likely to undergo HF elimination. Termination of radical intermediates can either be recombination with a CF₃ radical or hydrogen abstraction (H-abstraction). Observed hydrogen-substituted products indicate that functional groups with higher hydrocarbon character may lead to more H-abstraction terminated products. Overall findings show that the functional group of a PFAS may decrease or increase its thermal stability and lead to different profiles of pyrolysis products.