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. 2020 Dec 31;93(6):826–843. doi: 10.1002/wer.1483

Table 4.

PFAS thermal degradation by‐products reported

Reference Parent PFAS Treatment temperature Atmosphere Fluorinated by‐products notedA
NRC Alaska (2019) PFOS and PFOA (measured in contaminated soil sample)

425–815°C (kiln)

980–1,200°C (secondary combustion)

Oxidizing PFBA, PFPeA, PFHxA, PFHpA, PFOA, PFNA, PFDA, PFDoA, PFTeA, PFBS, FOSA, PFUnA, PFHxS, PFOS, NMeFOSAA, NEtFOSAA, 6:2 FTS
Major (2019) PFOA, PFOS, PFHxS, PFNA, PFBS, and PFHpA 1,000°C Oxidizing PFBA, PFBS, PFPeA, PFHxA, PFHxS, PFHpA, PFOA, PFOS, PFNA, PFDA, PFUnA, PFDoA
Watanabe et al. (2018) PFOA, PFHxA, PFOS (on GAC) 700°C Reducing Incomplete balance suggests volatile organofluoro compounds
Watanabe et al. (2016)

PFOA, PFHxA (on GAC)

PFOS (on GAC)

800°C

900°C

1,000°C

700–1,000°C

Reducing

PFPeA, PFBA

PFBA

None

None

García et al. (2007) PTFE

750°C

850°C

950°C

1,050°C

Oxidizing

CF4, C2F6, benzoyl fluoride

CF4, C2F6

CF4, C2F6, C3F6, benzenepentafluoro

CF4, C2F6, benzenepentafluoro

Yamada et al. (2005)

Fluorotelomer‐based acrylic polymer (C0.33H0.40O0.04F0.19Cl0.04)

Treated polyester fiber (2% F by weight)

600°C

1,000°C

725°C

Oxidizing

Flurobenzene, difluorobenzene, ·CF3, ·CF2CH=CH2

·CF3, ·CF2CH=CH2

·CF3

Krusic et al. (2005) PFOA

307°C

355–385°C

Vacuum

Perfluoro‐1‐heptene

1‐H‐perfluoroheptane, perfluoro‐1‐heptene

Krusic and Roe (2004) Ammonium PFOA 196–234°C Vacuum 1‐H‐perfluoroheptane
Ellis et al. (2003) PTFE 550°C Oxidizing fluoroacids
Taylor and Yamada (2003) PFOS

600°C

900°C

Oxidizing

CF4 or C2F6 (postulated), 1,1‐difluroethene

CF4 or C2F6 (postulated)

Ellis et al. (2001) PTFE 500°C Oxidizing Tetrafluoroethene, hexafluoropropene, trifluoroacetate, cyclo‐octafluorobutane, CF3(CF2)nCOOH, CF3O(CF2)mCOOH, monofluoracetic acid, difluoroacetic acid
Conesa and Font (2001) PTFE 700°C Oxidizing C2F2, C2F4, CF4, CHF3, CH2F2, C2F6, ·CFO, CH2F2, cyclo‐C4F8, C3F3
Reducing same
Simon and Kaminsky (1998) PTFE 500–600°C Reducing Trifluroethylene, hexafluroproprene, cyclo‐octafluorobutane
Jun et al. (1995) PTFE 510–600°C Reducing Tetrafluoroethylene, hexafluroproprene, cyclo‐octafluorobutane
Baker and Kasprzak (1993) PTFE 400°C

Oxidizing

Reducing

Tetrafluoroethylene, hexafluropropylene, trifluoroacetyl fluoride, fluoroform, perfluoroisobutylene

hexafluropropylene, perfluoroisobutylene

Blake and Tomlinson (1971) Fluoroacetic acid 295–382°C Vacuum Fluoroacetyl fluoride
Sheppard and Sharts (1969), Kissa (2001) Perfluoroalkanoic acid 550°C Not identified Perfluoroalkenes, hydrogen fluoride
Perfluoroalkanoic potassium salt 165–200°C Perfluoroalkenes
Scheel et al. (1968) PTFE 550°C Reducing Carbonyl fluoride
Lewis and Naylor (1947) PTFE 600–700°C Reducing Tetrafluoroethylene
A

Compound acronym definition can be found in the source reference.