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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creator | 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. |
description | 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%. |
doi_str_mv | 10.1016/j.jfluchem.2016.10.004 |
format | Article |
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[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%.</description><identifier>ISSN: 0022-1139</identifier><identifier>EISSN: 1873-3328</identifier><identifier>DOI: 10.1016/j.jfluchem.2016.10.004</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Acid-base neutralization ; Calorimetry ; Chemical compounds ; Chlorodifluoromethane ; Crystallography ; Differential scanning calorimetry ; Electron microscopy ; Fourier transforms ; Hazards ; Heat measurement ; Infrared spectrophotometers ; Institutions ; Mass spectrometry ; Mass spectroscopy ; Neutralization ; NMR ; Nuclear magnetic resonance ; Potassium ; Pyrolysis ; Salt ; Salts ; Scanning electron microscopy ; Single crystals ; Spectrophotometry ; Spectroscopy ; Synthesis and pyrolysis of potassium pentafluoropropionate ; Tetrafluoroethylene ; Tetrafluoroethylene (TFE) ; Tetrafluoroethylene-carbon dioxide mixture ; Thermal analysis ; Thermogravimetric analysis ; Use of TFE in academic institutions ; Vacuum ; X-ray crystallography ; X-ray diffraction</subject><ispartof>Journal of fluorine chemistry, 2017-04, Vol.196 (C), p.107-116</ispartof><rights>2016 Elsevier B.V.</rights><rights>Copyright Elsevier BV Apr 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-b1a5aad8fa5b473b2dd83b93f5194454979724656cdd6064a91dd1bd4ae9ff3e3</citedby><cites>FETCH-LOGICAL-c481t-b1a5aad8fa5b473b2dd83b93f5194454979724656cdd6064a91dd1bd4ae9ff3e3</cites><orcidid>0000-0003-1479-1897 ; 0000000314791897</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022113916303591$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/1413793$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Hercules, Daniel A.</creatorcontrib><creatorcontrib>Parrish, Cameron A.</creatorcontrib><creatorcontrib>Sayler, Todd S.</creatorcontrib><creatorcontrib>Tice, Kevin T.</creatorcontrib><creatorcontrib>Williams, Shane M.</creatorcontrib><creatorcontrib>Lowery, Lauren E.</creatorcontrib><creatorcontrib>Brady, Michael E.</creatorcontrib><creatorcontrib>Coward, Robert B.</creatorcontrib><creatorcontrib>Murphy, Justin A.</creatorcontrib><creatorcontrib>Hey, Trevyn A.</creatorcontrib><creatorcontrib>Scavuzzo, Anthony R.</creatorcontrib><creatorcontrib>Rummler, Lucy M.</creatorcontrib><creatorcontrib>Burns, Emory G.</creatorcontrib><creatorcontrib>Matsnev, Andrej V.</creatorcontrib><creatorcontrib>Fernandez, Richard E.</creatorcontrib><creatorcontrib>McMillen, Colin D.</creatorcontrib><creatorcontrib>Thrasher, Joseph S.</creatorcontrib><title>Preparation of tetrafluoroethylene from the pyrolysis of pentafluoropropionate salts</title><title>Journal of fluorine chemistry</title><description>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%.</description><subject>Acid-base neutralization</subject><subject>Calorimetry</subject><subject>Chemical compounds</subject><subject>Chlorodifluoromethane</subject><subject>Crystallography</subject><subject>Differential scanning calorimetry</subject><subject>Electron microscopy</subject><subject>Fourier transforms</subject><subject>Hazards</subject><subject>Heat measurement</subject><subject>Infrared spectrophotometers</subject><subject>Institutions</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Neutralization</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Potassium</subject><subject>Pyrolysis</subject><subject>Salt</subject><subject>Salts</subject><subject>Scanning electron microscopy</subject><subject>Single crystals</subject><subject>Spectrophotometry</subject><subject>Spectroscopy</subject><subject>Synthesis and pyrolysis of potassium pentafluoropropionate</subject><subject>Tetrafluoroethylene</subject><subject>Tetrafluoroethylene (TFE)</subject><subject>Tetrafluoroethylene-carbon dioxide mixture</subject><subject>Thermal analysis</subject><subject>Thermogravimetric analysis</subject><subject>Use of TFE in academic institutions</subject><subject>Vacuum</subject><subject>X-ray crystallography</subject><subject>X-ray diffraction</subject><issn>0022-1139</issn><issn>1873-3328</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFkEtLxDAUhYMoOI7-BSm6bk2a9JGdMviCAV2M65AmN7Sl09QkI8y_N6XjWrgQ7uU7h5OD0C3BGcGkfOiz3gwH1cI-y-MejxnG7AytSF3RlNK8PkcrjPM8JYTyS3TlfY8xrnBVr9Du08EknQydHRNrkgDByWhnnYXQHgcYITHO7pPQQjIdnR2OvvMzOcEYTuQUJ-plgMTLIfhrdGHk4OHm9K7R18vzbvOWbj9e3zdP21SxmoS0IbKQUtdGFg2raJNrXdOGU1MQzljBeMWrnJVFqbQucckkJ1qTRjMJ3BgKdI3uFl_rQye86gKoVtlxBBUEYYRWnEbofoFiyu8D-CB6e3BjzCUIpxXlNS_qSJULpZz13oERk-v20h0FwWKuWfTir2Yx1zzfY81R-LgIIX70pwM354BRge7cHEPb7j-LX1yvi4Q</recordid><startdate>20170401</startdate><enddate>20170401</enddate><creator>Hercules, Daniel A.</creator><creator>Parrish, Cameron A.</creator><creator>Sayler, Todd S.</creator><creator>Tice, Kevin T.</creator><creator>Williams, Shane M.</creator><creator>Lowery, Lauren E.</creator><creator>Brady, Michael E.</creator><creator>Coward, Robert 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BV</general><general>Elsevier</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>7U7</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0003-1479-1897</orcidid><orcidid>https://orcid.org/0000000314791897</orcidid></search><sort><creationdate>20170401</creationdate><title>Preparation of tetrafluoroethylene from the pyrolysis of pentafluoropropionate salts</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-b1a5aad8fa5b473b2dd83b93f5194454979724656cdd6064a91dd1bd4ae9ff3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acid-base neutralization</topic><topic>Calorimetry</topic><topic>Chemical compounds</topic><topic>Chlorodifluoromethane</topic><topic>Crystallography</topic><topic>Differential scanning calorimetry</topic><topic>Electron microscopy</topic><topic>Fourier transforms</topic><topic>Hazards</topic><topic>Heat measurement</topic><topic>Infrared spectrophotometers</topic><topic>Institutions</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Neutralization</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Potassium</topic><topic>Pyrolysis</topic><topic>Salt</topic><topic>Salts</topic><topic>Scanning electron microscopy</topic><topic>Single crystals</topic><topic>Spectrophotometry</topic><topic>Spectroscopy</topic><topic>Synthesis and pyrolysis of potassium pentafluoropropionate</topic><topic>Tetrafluoroethylene</topic><topic>Tetrafluoroethylene (TFE)</topic><topic>Tetrafluoroethylene-carbon dioxide mixture</topic><topic>Thermal analysis</topic><topic>Thermogravimetric analysis</topic><topic>Use of TFE in academic institutions</topic><topic>Vacuum</topic><topic>X-ray crystallography</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hercules, Daniel A.</creatorcontrib><creatorcontrib>Parrish, Cameron A.</creatorcontrib><creatorcontrib>Sayler, Todd S.</creatorcontrib><creatorcontrib>Tice, Kevin T.</creatorcontrib><creatorcontrib>Williams, Shane M.</creatorcontrib><creatorcontrib>Lowery, Lauren E.</creatorcontrib><creatorcontrib>Brady, Michael E.</creatorcontrib><creatorcontrib>Coward, Robert B.</creatorcontrib><creatorcontrib>Murphy, Justin A.</creatorcontrib><creatorcontrib>Hey, Trevyn A.</creatorcontrib><creatorcontrib>Scavuzzo, Anthony R.</creatorcontrib><creatorcontrib>Rummler, Lucy M.</creatorcontrib><creatorcontrib>Burns, Emory G.</creatorcontrib><creatorcontrib>Matsnev, Andrej V.</creatorcontrib><creatorcontrib>Fernandez, Richard E.</creatorcontrib><creatorcontrib>McMillen, Colin D.</creatorcontrib><creatorcontrib>Thrasher, Joseph S.</creatorcontrib><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications 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Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>OSTI.GOV</collection><jtitle>Journal of fluorine chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hercules, Daniel A.</au><au>Parrish, Cameron A.</au><au>Sayler, Todd S.</au><au>Tice, Kevin T.</au><au>Williams, Shane M.</au><au>Lowery, Lauren E.</au><au>Brady, Michael E.</au><au>Coward, Robert B.</au><au>Murphy, Justin A.</au><au>Hey, Trevyn A.</au><au>Scavuzzo, Anthony R.</au><au>Rummler, Lucy M.</au><au>Burns, Emory G.</au><au>Matsnev, Andrej V.</au><au>Fernandez, Richard E.</au><au>McMillen, Colin D.</au><au>Thrasher, Joseph S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of tetrafluoroethylene from the pyrolysis of pentafluoropropionate salts</atitle><jtitle>Journal of fluorine chemistry</jtitle><date>2017-04-01</date><risdate>2017</risdate><volume>196</volume><issue>C</issue><spage>107</spage><epage>116</epage><pages>107-116</pages><issn>0022-1139</issn><eissn>1873-3328</eissn><abstract>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%.</abstract><cop>Lausanne</cop><pub>Elsevier B.V</pub><doi>10.1016/j.jfluchem.2016.10.004</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-1479-1897</orcidid><orcidid>https://orcid.org/0000000314791897</orcidid><oa>free_for_read</oa></addata></record> |
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source | ScienceDirect Journals (5 years ago - present) |
subjects | Acid-base neutralization Calorimetry Chemical compounds Chlorodifluoromethane Crystallography Differential scanning calorimetry Electron microscopy Fourier transforms Hazards Heat measurement Infrared spectrophotometers Institutions Mass spectrometry Mass spectroscopy Neutralization NMR Nuclear magnetic resonance Potassium Pyrolysis Salt Salts Scanning electron microscopy Single crystals Spectrophotometry Spectroscopy Synthesis and pyrolysis of potassium pentafluoropropionate Tetrafluoroethylene Tetrafluoroethylene (TFE) Tetrafluoroethylene-carbon dioxide mixture Thermal analysis Thermogravimetric analysis Use of TFE in academic institutions Vacuum X-ray crystallography X-ray diffraction |
title | Preparation of tetrafluoroethylene from the pyrolysis of pentafluoropropionate salts |
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