1963
DOI: 10.1021/ac60200a049
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Separation of Some Low Molecular Weight Fluorocarbons by Gas Chromatography.

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Cited by 21 publications
(6 citation statements)
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“…The identity of the two minor peaks, due to ^2^2 * ^4 ^8 ' confirmed due to lack of • reference gases (2). Duplicate chromatograms for identical sample mixtures were reproducible within ±1,5% for major components.…”
Section: Resultsmentioning
confidence: 78%
“…The identity of the two minor peaks, due to ^2^2 * ^4 ^8 ' confirmed due to lack of • reference gases (2). Duplicate chromatograms for identical sample mixtures were reproducible within ±1,5% for major components.…”
Section: Resultsmentioning
confidence: 78%
“…4 We were not able to identify iso-C 5 F 10 as (CF 3 ) 4 C or as (CF 3 ) 2 CF-CF 2 -CF 3 . 5 Per F-heptane I and per F-heptane II are both branched heptanes of unknown structure.…”
Section: Resultsmentioning
confidence: 99%
“…Ne and CF 4 were obtained from Matheson Gas Products, C 3 F 6 and CH 2 F 2 from Peninsular Chemical Research, CHF 3 , CH 3 F and C 2 F 6 from Baker. Perfluoro-isobutene was prepared by pyrolysis of c-C 4 F g [5]. Organic purity was monitored by VPC analysis; no impurities could be detected.…”
Section: Methodsmentioning
confidence: 99%
“…Analysis was carried out, using a Burrell Kromo Tog Model K D vapor phase chromatograph on a 10 foot silica gel column (9), operating between 50 and 275 "C, with thermal conductivity detectors. The instrument was calibrated with known quantities of each of the perfluorocarbons found in the photolysis (apart from difluoroacetylene, which is unstable even at low concentrations (10)).…”
Section: Methodsmentioning
confidence: 99%
“…It is difficult to justify exclusively a mechanism for the formation of perfluoropropane. Reactions [7] to [9] indicate a probable pathway3 3The authors are grateful to a referee for suggesting this mechanism.…”
Section: Difluoromethyiene Reactionsmentioning
confidence: 99%