The contribution of fluoropolymer thermolysis to trifluoroacetic acid (TFA) in environmental media.
Contribution
Fluorompolymer
Pyrolysis
Rainwater
Trifluoroacetic acid
Journal
Chemosphere
ISSN: 1879-1298
Titre abrégé: Chemosphere
Pays: England
ID NLM: 0320657
Informations de publication
Date de publication:
May 2019
May 2019
Historique:
received:
19
11
2018
revised:
27
01
2019
accepted:
29
01
2019
pubmed:
8
2
2019
medline:
4
4
2019
entrez:
8
2
2019
Statut:
ppublish
Résumé
The source of trifluoroacetic acid (TFA) has long been a controversial issue. Fluoropolymer thermolysis is expected to be a potential anthropogenic source except for CFC alternatives. However, its TFA yield and contributions have rarely been reported more recently. In this study, we investigated the thermal properties of three kinds of fluoropolymers, including poly (vinylidene fluoride-co-hexafluropropylene) (PVDF-HFP), poly (vinylidene fluoride-co-chlorotrifluoroethylene) (PVDF-CTFE) and poly (tetrafluoroethylene) (PTFE). A laboratory simulation experiment was then performed to analyze the TFA levels in the thermolysis products and hence to examine the TFA yields of these fluoropolymers. Thermolysis of these fluoropolymers occurred in the temperature ranges from ∼400 °C to ∼650 °C, with the peak weight loss rate at around 550-600 °C. TFA could be produced through fluoropolymer thermolysis when being heated to 500 °C and above. Average TFA yields of PTFE, PVDF-HFP and PVDF-CTFE were 1.2%, 0.9% and 0.3%, respectively. Furthermore, the contribution of fluoropolymer thermolysis and CFC alternatives to rainwater TFA in Beijing, China was evaluated by using a Two-Box model. The degradation of fluoropolymers and HCFCs/HFCs could explain 37.9-43.4 ng L
Identifiants
pubmed: 30731384
pii: S0045-6535(19)30193-6
doi: 10.1016/j.chemosphere.2019.01.174
pii:
doi:
Substances chimiques
Chlorofluorocarbons
0
Fluorocarbons
0
Polymers
0
chlorotrifluoroethylene
AF215GW34G
Trifluoroacetic Acid
E5R8Z4G708
tetrafluoroethylene
OMW63Z518S
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
637-644Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.