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Updated: Jun 12, 2025

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
Published on: December 16, 2022
Repurposing HFC-125 to tetrafluoroethylene: A step toward a more sustainable fluoropolymer feedstock strategy
Hiroto Iwasaki1, Naoyuki Hoshiya2, Yosuke Kishikawa2
1Department of Nanopharmaceutical Sciences, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan.
Abstract:
The urgency to reduce hydrofluorocarbon (HFC) emissions, particularly HFC-125 (pentafluoroethane, CF3CF2H), has driven efforts to develop sustainable alternatives. Herein, we present a method for converting HFC-125 into tetrafluoroethylene (TFE), an industrially valuable monomer for fluoropolymer production. Our approach uses potassium hexamethyldisilazide (KHMDS), optimizing reaction conditions at -50°C to achieve high TFE yields without any observable byproducts. This low-temperature method offers a safer and more sustainable alternative to traditional high-temperature processes for TFE production, which involve hazardous byproducts and complex handling. We also demonstrated that various chemical reactions using freshly generated TFE, including thiol addition, trifluorovinylation, radical addition, amination, alcohol addition, and polymerization, can be performed, extending the utility of this approach. Moreover, a continuous flow process for the conversion of HFC-125 to TFE at room temperature was achieved without cryogenic equipment. This dual-purpose solution addresses both environmental sustainability of fluorochemicals and the growing demand for fluoropolymers in various industries.
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