An Experimental Study of the Formation of Perfluoroisobutene

This paper presents an experimental study that focuses on the formation of perfluoroisobutene (i-C 4 Fg). Experiments were carried out at atmospheric pressure in a quartz flow tube reactor over the temperature range of 823 to 1273K and an initial reactant feed concentration of 2% with the balance ni...

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Veröffentlicht in:Combustion science and technology 1998-05, Vol.134 (1-6), p.65-85
Hauptverfasser: Salmon, R. P., Difelice, J. J., Ritter, E. R.
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Ritter, E. R.
description This paper presents an experimental study that focuses on the formation of perfluoroisobutene (i-C 4 Fg). Experiments were carried out at atmospheric pressure in a quartz flow tube reactor over the temperature range of 823 to 1273K and an initial reactant feed concentration of 2% with the balance nitrogen. Reactants studied include chlorodifluoromethane (CHF 2 Cl), 1,1,1,2-tetrafluoro-2-chloroethane (CF 3 CHFCl), trifluoromethane (CHF 3 ), perfluoropropene (C 3 F 6 ), and mixtures of these species. Effluent gas concentrations were obtained using a water cooled gas sampling probe, and analysis of products was performed via on line gas chromatography with flame ionization detection and gas chromatography with mass selective detection. C 3 F 6 pyrolysis produced more than 22% i-C.F, yield, while mixtures with CHF 2 Cl and CHF 3 resulted in i-C 4 F g yields of 14% and 28%, respectively. The pyrolysis of CF3CHFCI resulted in slightly greater than 6% i-C 4 F g yield, and CHF 2 Cl decomposition produced up to 6% i-C 4 F g yield, while CHF 2 Cl/CF 3 CHFC1 copyrolysis produced 8% yield of i-C 4 F g . These results show that the addition of a difluoromethylene (iCF 2 ) source increases i-C 4 F g production. This suggests that a major pathway to i-C 4 F g production may be C 3 F 6 isomerization to singlet perfluorodimethylcarbene (l:C(CF 3 ) 2 ) and subsequent collisional stabilization to the triplet carbene (3:C(CF 3 ) 2 ) followed by either 1:CF 2 addition or further reaction with C 3 F 6 . This work focuses on an experimental study. Detailed modeling work is ongoing.
doi_str_mv 10.1080/00102209808924126
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P. ; Difelice, J. J. ; Ritter, E. R.</creator><creatorcontrib>Salmon, R. P. ; Difelice, J. J. ; Ritter, E. R.</creatorcontrib><description>This paper presents an experimental study that focuses on the formation of perfluoroisobutene (i-C 4 Fg). Experiments were carried out at atmospheric pressure in a quartz flow tube reactor over the temperature range of 823 to 1273K and an initial reactant feed concentration of 2% with the balance nitrogen. Reactants studied include chlorodifluoromethane (CHF 2 Cl), 1,1,1,2-tetrafluoro-2-chloroethane (CF 3 CHFCl), trifluoromethane (CHF 3 ), perfluoropropene (C 3 F 6 ), and mixtures of these species. Effluent gas concentrations were obtained using a water cooled gas sampling probe, and analysis of products was performed via on line gas chromatography with flame ionization detection and gas chromatography with mass selective detection. C 3 F 6 pyrolysis produced more than 22% i-C.F, yield, while mixtures with CHF 2 Cl and CHF 3 resulted in i-C 4 F g yields of 14% and 28%, respectively. The pyrolysis of CF3CHFCI resulted in slightly greater than 6% i-C 4 F g yield, and CHF 2 Cl decomposition produced up to 6% i-C 4 F g yield, while CHF 2 Cl/CF 3 CHFC1 copyrolysis produced 8% yield of i-C 4 F g . These results show that the addition of a difluoromethylene (iCF 2 ) source increases i-C 4 F g production. This suggests that a major pathway to i-C 4 F g production may be C 3 F 6 isomerization to singlet perfluorodimethylcarbene (l:C(CF 3 ) 2 ) and subsequent collisional stabilization to the triplet carbene (3:C(CF 3 ) 2 ) followed by either 1:CF 2 addition or further reaction with C 3 F 6 . This work focuses on an experimental study. 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P.</creatorcontrib><creatorcontrib>Difelice, J. J.</creatorcontrib><creatorcontrib>Ritter, E. R.</creatorcontrib><title>An Experimental Study of the Formation of Perfluoroisobutene</title><title>Combustion science and technology</title><description>This paper presents an experimental study that focuses on the formation of perfluoroisobutene (i-C 4 Fg). Experiments were carried out at atmospheric pressure in a quartz flow tube reactor over the temperature range of 823 to 1273K and an initial reactant feed concentration of 2% with the balance nitrogen. Reactants studied include chlorodifluoromethane (CHF 2 Cl), 1,1,1,2-tetrafluoro-2-chloroethane (CF 3 CHFCl), trifluoromethane (CHF 3 ), perfluoropropene (C 3 F 6 ), and mixtures of these species. Effluent gas concentrations were obtained using a water cooled gas sampling probe, and analysis of products was performed via on line gas chromatography with flame ionization detection and gas chromatography with mass selective detection. C 3 F 6 pyrolysis produced more than 22% i-C.F, yield, while mixtures with CHF 2 Cl and CHF 3 resulted in i-C 4 F g yields of 14% and 28%, respectively. The pyrolysis of CF3CHFCI resulted in slightly greater than 6% i-C 4 F g yield, and CHF 2 Cl decomposition produced up to 6% i-C 4 F g yield, while CHF 2 Cl/CF 3 CHFC1 copyrolysis produced 8% yield of i-C 4 F g . These results show that the addition of a difluoromethylene (iCF 2 ) source increases i-C 4 F g production. This suggests that a major pathway to i-C 4 F g production may be C 3 F 6 isomerization to singlet perfluorodimethylcarbene (l:C(CF 3 ) 2 ) and subsequent collisional stabilization to the triplet carbene (3:C(CF 3 ) 2 ) followed by either 1:CF 2 addition or further reaction with C 3 F 6 . This work focuses on an experimental study. Detailed modeling work is ongoing.</description><subject>Air pollution caused by fuel industries</subject><subject>Applied sciences</subject><subject>Energy</subject><subject>Energy. 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Control</topic><topic>Perfluoroisobutene</topic><topic>pyrolysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salmon, R. P.</creatorcontrib><creatorcontrib>Difelice, J. J.</creatorcontrib><creatorcontrib>Ritter, E. R.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Combustion science and technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salmon, R. P.</au><au>Difelice, J. J.</au><au>Ritter, E. R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An Experimental Study of the Formation of Perfluoroisobutene</atitle><jtitle>Combustion science and technology</jtitle><date>1998-05-01</date><risdate>1998</risdate><volume>134</volume><issue>1-6</issue><spage>65</spage><epage>85</epage><pages>65-85</pages><issn>0010-2202</issn><eissn>1563-521X</eissn><coden>CBSTB9</coden><abstract>This paper presents an experimental study that focuses on the formation of perfluoroisobutene (i-C 4 Fg). Experiments were carried out at atmospheric pressure in a quartz flow tube reactor over the temperature range of 823 to 1273K and an initial reactant feed concentration of 2% with the balance nitrogen. Reactants studied include chlorodifluoromethane (CHF 2 Cl), 1,1,1,2-tetrafluoro-2-chloroethane (CF 3 CHFCl), trifluoromethane (CHF 3 ), perfluoropropene (C 3 F 6 ), and mixtures of these species. Effluent gas concentrations were obtained using a water cooled gas sampling probe, and analysis of products was performed via on line gas chromatography with flame ionization detection and gas chromatography with mass selective detection. C 3 F 6 pyrolysis produced more than 22% i-C.F, yield, while mixtures with CHF 2 Cl and CHF 3 resulted in i-C 4 F g yields of 14% and 28%, respectively. The pyrolysis of CF3CHFCI resulted in slightly greater than 6% i-C 4 F g yield, and CHF 2 Cl decomposition produced up to 6% i-C 4 F g yield, while CHF 2 Cl/CF 3 CHFC1 copyrolysis produced 8% yield of i-C 4 F g . These results show that the addition of a difluoromethylene (iCF 2 ) source increases i-C 4 F g production. This suggests that a major pathway to i-C 4 F g production may be C 3 F 6 isomerization to singlet perfluorodimethylcarbene (l:C(CF 3 ) 2 ) and subsequent collisional stabilization to the triplet carbene (3:C(CF 3 ) 2 ) followed by either 1:CF 2 addition or further reaction with C 3 F 6 . This work focuses on an experimental study. Detailed modeling work is ongoing.</abstract><cop>London</cop><pub>Taylor &amp; Francis Group</pub><doi>10.1080/00102209808924126</doi><tpages>21</tpages></addata></record>
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subjects Air pollution caused by fuel industries
Applied sciences
Energy
Energy. Thermal use of fuels
Exact sciences and technology
gas chromatograph
gas chromatography
Metering. Control
Perfluoroisobutene
pyrolysis
title An Experimental Study of the Formation of Perfluoroisobutene
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