Preparation of tetrafluoroethylene from the pyrolysis of pentafluoropropionate salts

Typical yields of TFE obtained from pyrolysis of potassium pentafluoropropionate obtained from the acid-base neutralization method are >98%. [Display omitted] •Equimolar mixtures of tetrafluoroethylene and carbon dioxide were prepared.•Higher yields of TFE than previous literature reports by this...

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Veröffentlicht in:Journal of fluorine chemistry 2017-04, Vol.196 (C), p.107-116
Hauptverfasser: Hercules, Daniel A., Parrish, Cameron A., Sayler, Todd S., Tice, Kevin T., Williams, Shane M., Lowery, Lauren E., Brady, Michael E., Coward, Robert B., Murphy, Justin A., Hey, Trevyn A., Scavuzzo, Anthony R., Rummler, Lucy M., Burns, Emory G., Matsnev, Andrej V., Fernandez, Richard E., McMillen, Colin D., Thrasher, Joseph S.
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Sprache:eng
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Zusammenfassung:Typical yields of TFE obtained from pyrolysis of potassium pentafluoropropionate obtained from the acid-base neutralization method are >98%. [Display omitted] •Equimolar mixtures of tetrafluoroethylene and carbon dioxide were prepared.•Higher yields of TFE than previous literature reports by this route are reported.•The method based on the pyrolysis of potassium pentafluoropropionate is preferred.•A higher purity of the tetrafluoroethylene/carbon dioxide mixture was obtained.•This method of preparation of tetrafluoroethylene is suitable for academic institutions. The use of tetrafluoroethylene (TFE) in academic institutions beyond a few millimoles has often been inhibited by the compound's inherent danger and general lack of commercial availability. On the other hand, TFE is prepared industrially on a rather large scale by a number of major fluorochemical companies via the pyrolysis of chlorodifluoromethane at high temperatures, yielding TFE and HCl. For a few years at The University of Alabama and Clemson University, we have been preparing TFE on a 100+-gram scale by the pyrolysis under dynamic vacuum of pentafluoropropionate salts, which can be obtained from the neutralization of pentafluoropropionic acid with a M(OH)n (where M=Li, Na, K, and Cs for n=1 and Mg, Ca, and Ba for n=2). Additionally, potassium pentafluoropropionate can be prepared from the reaction of potassium trimethylsilanolate and ethyl pentafluoropropionate. The pentafluoropropionate salts and their decomposition products have been characterized by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), accelerating rate calorimetry (ARC), nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry, Fourier transform-infrared (FTIR) spectrophotometry, scanning electron microscopy (SEM)/energy dispersive spectroscopy (EDAX), X-ray diffraction (XRD), and single-crystal X-ray crystallography, where applicable. Typical yields of TFE obtained from pyrolysis of potassium pentafluoropropionate obtained from the acid-base neutralization method are >98%, while yields of TFE from the same salt prepared by the silanolate method from ethyl pentafluoropropionate are ca. 80%.
ISSN:0022-1139
1873-3328
DOI:10.1016/j.jfluchem.2016.10.004