Verfahren zur Herstellung von Hexafluorpropan und Perfluorpropan
Perfluoroisobutene-MeOH adduct (2H-octafluoroisobutyl methyl ether) converted to hexafluoropropane by reaction with trialkyl amine (e.g., triethylamine) and H2O. 1,1,1,3,3-Pentafluoropropene also produced in lesser amounts. Electrolysis of reaction product in anhydrous HF (at 10 - 50 C, 0 - 140 kPa,...
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creator | HANSEN, JOHN C CHEBURKOV, YURI |
description | Perfluoroisobutene-MeOH adduct (2H-octafluoroisobutyl methyl ether) converted to hexafluoropropane by reaction with trialkyl amine (e.g., triethylamine) and H2O. 1,1,1,3,3-Pentafluoropropene also produced in lesser amounts. Electrolysis of reaction product in anhydrous HF (at 10 - 50 C, 0 - 140 kPa, and 50 - 300 amps/m anode area) yields C3F8 and some CF3CFHCF3 condensed out of gas stream from electrolysis cell. |
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Electrolysis of reaction product in anhydrous HF (at 10 - 50 C, 0 - 140 kPa, and 50 - 300 amps/m anode area) yields C3F8 and some CF3CFHCF3 condensed out of gas stream from electrolysis cell.</description><edition>7</edition><language>ger</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; APPARATUS THEREFOR ; CHEMISTRY ; ELECTROLYTIC OR ELECTROPHORETIC PROCESSES ; ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTIONOF COMPOUNDS OR NON-METALS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2000</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20000302&DB=EPODOC&CC=DE&NR=69512288T2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20000302&DB=EPODOC&CC=DE&NR=69512288T2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>HANSEN, JOHN C</creatorcontrib><creatorcontrib>CHEBURKOV, YURI</creatorcontrib><title>Verfahren zur Herstellung von Hexafluorpropan und Perfluorpropan</title><description>Perfluoroisobutene-MeOH adduct (2H-octafluoroisobutyl methyl ether) converted to hexafluoropropane by reaction with trialkyl amine (e.g., triethylamine) and H2O. 1,1,1,3,3-Pentafluoropropene also produced in lesser amounts. 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Electrolysis of reaction product in anhydrous HF (at 10 - 50 C, 0 - 140 kPa, and 50 - 300 amps/m anode area) yields C3F8 and some CF3CFHCF3 condensed out of gas stream from electrolysis cell.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS APPARATUS THEREFOR CHEMISTRY ELECTROLYTIC OR ELECTROPHORETIC PROCESSES ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTIONOF COMPOUNDS OR NON-METALS METALLURGY ORGANIC CHEMISTRY |
title | Verfahren zur Herstellung von Hexafluorpropan und Perfluorpropan |
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