Method for preparing hexafluoroethane
A technology of hexafluoroethane and monochloropentafluoroethane, which is applied in the field of preparation of hexafluoroethane, can solve the problems of severe heat release, poor catalyst selectivity, and difficulties in industrial production
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Embodiment 1
[0027] For pentafluoroethane industrialized units, mixtures of pentafluoroethane, monochloropentafluoroethane, dichlorotetrafluoroethane, tetrafluoroethane, trifluoroethane, extractant and other mixtures obtained through extraction and separation, after purification Distillation, drying, gas chromatographic analysis of the distillate, the results are as listed in Table 1, the composition of crude chloropentafluoroethane, no chlorotrifluoromethane was detected.
[0028] Table 1
[0029] composition CF 3 CHF 2 CF 3 CH 2 f CF 3 CCIF 2 CF 3 CCl 2 f Content (V%) 0.74 0.05 98.26 0.95
preparation Embodiment 1
[0030] Catalyst preparation example 1: Cr-Mg-Al catalyst
[0031] Chromium chloride and magnesium nitrate are dissolved in pure water, wherein the weight ratio of chromium:magnesium is 19:1, and a mixed solution with a concentration of 20% is made, and reacted with ammonia solution with a concentration of 5%, and the pH value of the reaction solution is 8.5~ Stop adding ammonia water at 9.5, filter the resulting hydroxide precipitate, wash thoroughly with pure water, then dry the obtained co-precipitate at 120°C, knead with aluminum fluoride:precipitate at a weight ratio of 1:5, and extrude with an extruder The strips are formed, and the strip particles made are loaded into the catalyst burner, and the N 2 Ignition in air flow (gradually increase the temperature to 400°C) to obtain the catalyst precursor. Cool down to 100°C with nitrogen gas, start to use N 2 Dilute HF atmosphere for fluorination (gradually increase the temperature to 450°C), pass N after fluorination 2 C...
preparation Embodiment 2
[0032] Catalyst preparation example 2: Cr-Al catalyst
[0033] Dissolve chromium chloride in pure water to make a solution of 20% concentration, and react with 5% ammonia solution by stirring. When the pH value of the reaction solution is 8.5 to 9.0, stop adding 5% ammonia water, and filter the produced hydrogen to oxidize The precipitate was washed thoroughly with pure water, and then the obtained precipitate was dried at 120°C. The aluminum fluoride and the precipitate were kneaded at a weight ratio of 1:5, extruded with an extruder, and the strip-shaped particles were packed into Catalyst burner, in N 2 Ignition in air flow (gradually increase the temperature to 400°C) to obtain the catalyst precursor. Cool down to 100°C with nitrogen gas, start to use N 2 Dilute HF atmosphere for fluorination (gradually increase the temperature to 450°C), pass N after fluorination 2 Cool down to room temperature, seal the package, and prepare for use.
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