Reaktionsgleichung
[Cl:1][C:2]([Cl:8])([F:7])[C:3]([F:6])([F:5])[F:4].[Cl:9][C:10]([F:16])([F:15])[C:11]([Cl:14])([F:13])[F:12].[H][H].Cl.C(F)(F)C(F)F.C(F)(F)C(Cl)(F)F.C(F)C(F)(F)F.C(Cl)(F)C(F)(F)F>>[C:3]([F:6])([F:5])([F:4])[C:2]([Cl:8])([Cl:1])[F:7].[C:10]([Cl:9])([F:16])([F:15])[C:11]([Cl:14])([F:13])[F:12]Komponenten
Edukt 8
Produkt 1
Versuchsvorschrift
A mixture containing about 8% 2,2-dichloro-1,1,1,2-tetrafluoroethane (CFC-114a) and about 92% 1,2-dichloro-1,1,2,2-tetrafluoroethane (CFC-114) and hydrogen were fed to the reactor for a period of 477 hours. For an 11 hour period at 470° C., at an average time in synthesis of 67 hours, with a feed molar ratio of hydrogen to CFC-114/114a isomers of 2.1:1, and a liquid feed rate of 2.0 mL/hr of the combined 2,2-dichloro and the 1,2-dichloro isomers, the average conversion of the 2,2-dichloro isomer was 86% and the average conversion of the 1,2-dichloro isomer was 48%. The reactor effluent contained in addition to HCl and hydrogen, 2.3% HFC-134, 10.2% HCFC-124a and 13.9% CFC-114, as well as 0.4% HFC-134a, 1.6% HCFC-124 and 0.3% CFC-114a.
Aufarbeitung
- waitFor an 11 hour period at 470° C.
- customat an average time in synthesis of 67 hours
Quellen und Nachweise
- ORD-Eintrag
- ord-c0cbd90676e14e8fb958ead3358f6c91
- Quelldatensatz
- uspto-grants-1993_05
- Patentnummer
- US05208397
Verknüpfte Notizen
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