FIELD: industrial organic synthesis. SUBSTANCE: difluorochloromethane is subjected to pyrolysis in presence of steam and 1,1,2,2- tetrafluorochloroethane. Products are "quenched", freed of hydrochloric acid, neutralized, compressed, and condensed. Further, using multistage rectification, tetrafluoroethylene and fraction with boiling range from -42 to 0 C are isolated, the latter essentially containing difluorochloromethane, octafluorocyclobutane, 1,1,2,2- tetrafluorochloroethane, and hexafluoropropylene. These constituents are separated by water absorption and difluorochloromethane and 1,1,2,2- tetrafluorochloroethane are then desorbed and returned into pyrolysis process, whereas octafluorocyclobutane and hexafluoropropylene are isolated by rectifying non-absorbed gas fraction. Absorption is carried out in countercurrent mode at 5-25 C and pressure 3-7 atm in column-type apparatus passing water downward from the top and pyrolysis product from below at water-to-products weight ratio (50:150):1. EFFECT: enhanced process efficiency and new valuable product (octafluorocyclobutane) obtained. 2 cl, 2 tbl
| Title | Year | Author | Number | 
|---|---|---|---|
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 | RU2167847C1 | 
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 | RU2186052C1 | 
| METHOD OF SYNTHESIS OF TETRAFLUOROETHYLENE | 1991 | 
 | RU2097369C1 | 
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 | RU2162835C2 | 
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 | RU2097370C1 | 
Authors
Dates
1999-09-10—Published
1997-04-07—Filed