Processes for reducing the amount of monofluoroacetate in hydrofluoroolefin production
View Patent ↗A process is disclosed for reducing the amount of monofluoroacetate. The process involves (a) contacting a hydrofluorocarbon with a reactant basic aqueous solution to produce an organic phase solution containing a hydrofluoroolefin and an aqueous phase solution containing a monofluoroacetate; and (b) heating the aqueous phase solution to an effective temperature to reduce the amount of monofluoroacetate in the aqueous phase solution, wherein fluoride concentration in the aqueous phase solution is substantially high. Another process is disclosed for reducing the amount of monofluoroacetate. The process involves (a) contacting a first batch of hydrofluorocarbon with a first batch of reactant basic aqueous solution to produce a first batch of organic phase solution containing a hydrofluoroolefin and a first batch of aqueous phase solution containing a monofluoroacetate; (b) separating the first batch of organic phase solution from the first batch of aqueous phase solution; (c) mixing a second batch of hydrofluorocarbon and a second batch of reactant basic aqueous solution with the separated first batch of organic phase solution to produce a second batch of organic phase solution containing a hydrofluoroolefin and a second batch of aqueous phase solution containing a monofluoroacetate; (d) combining the first batch of aqueous phase solution with the second batch of aqueous phase solution; and (e) heating the combined aqueous phase solutions to an effective temperature to reduce the amount of monofluoroacetate in the combined aqueous phase solutions, wherein fluoride concentration in the combined aqueous phase solutions is substantially high.
1. A process for reducing the amount of monofluoroacetate in hydrofluoroolefin production, comprising:
(a) contacting a hydrofluorocarbon with a reactant basic aqueous solution to produce an organic phase solution comprising a hydrofluoroolefin and an aqueous phase solution comprising a monofluoroacetate;
(b) separating said aqueous phase solution from said organic phase solution; and
(c) heating said aqueous phase solution to an effective temperature to reduce the amount of monofluoroacetate in said aqueous phase solution, wherein fluoride concentration in said aqueous phase solution is at least 0.5 wt %.
2. The process of claim 1 wherein said hydrofluorocarbon is a hydrofluoropropane and said hydrofluoroolefin is a hydrofluoropropene.
3. The process of claim 2 wherein said hydrofluoropropane is 1,1,1,2,3-pentafluoropropane and said hydrofluoropropene is 2,3,3,3-tetrafluoro-1-propene.
4. The process of claim 2 wherein said hydrofluoropropane is 1,1,1,2,3,3-hexafluoropropane and said hydrofluoropropene is 1,2,3,3,3-pentafluoro-1-propene.
5. The process of claim 2 wherein said hydrofluoropropane is 1,1,1,3,3-pentafluoropropane and said hydrofluoropropene is 1,3,3,3-tetrafluoropropene.
6. The process of claim 1 wherein said aqueous phase solution is heated to a temperature of from about 80° C. to about 300° C.
7. The process of claim 1 wherein said aqueous phase solution is heated to a temperature of from about 100° C. to about 225° C.
8. The process of claim 1 wherein said aqueous phase solution is heated to a temperature of from about 125° C. to about 200° C.
9. The process of claim 1 wherein fluoride concentration in said aqueous phase solution is at least 5 wt %.
10. The process of claim 1 wherein fluoride concentration in said aqueous phase solution is at least 12 wt %.
11. The process of claim 1 wherein the total amount of monofluoroacetate in said aqueous phase solution is reduced to less than about 10 ppmw.
12. The process of claim 1 wherein the total amount of monofluoroacetate in said aqueous phase solution is reduced to less than about 5 ppmw.
13. The process of claim 1 wherein the total amount of monofluoroacetate in said aqueous phase solution is reduced to less than about 0.5 ppmw.
14. The process of claim 1 wherein said monofluoroacetate is FCH 2 COOK, FCH 2 COONa, or mixtures thereof.
15. The process of claim 1 wherein said reactant basic aqueous solution is made from an inorganic base.
16. The process of claim 15 wherein said inorganic base is sodium hydroxide, potassium hydroxide, or mixtures thereof.
17. The process of claim 1 wherein said hydrofluorocarbon contacts with said reactant basic aqueous solution in the presence of a phase transfer catalyst.
18. The process of claim 17 wherein said phase transfer catalyst is methyltri-n-octylammonium chloride, tetra-n-butylammonium bromide, or mixtures thereof.
19. The process of claim 1 wherein said hydrofluorocarbon contacts with said reactant basic aqueous solution in the presence of an organic solvent.
20. The process of claim 19 wherein said organic solvent is tetrahydrofuran.
21. A process for reducing the amount of monofluoroacetate in hydrofluoroolefin production, comprising:
(a) contacting a first batch of hydrofluorocarbon with a first batch of reactant basic aqueous solution to produce a first batch of organic phase solution comprising a hydrofluoroolefin and a first batch of aqueous phase solution comprising a monofluoroacetate;
(b) separating said first batch of organic phase solution from said first batch of aqueous phase solution;
(c) mixing a second batch of hydrofluorocarbon and a second batch of reactant basic aqueous solution with said separated first batch of organic phase solution to produce a second batch of organic phase solution comprising a hydrofluoroolefin and a second batch of aqueous phase solution comprising a monofluoroacetate;
(d) combining said first batch of aqueous phase solution with said second batch of aqueous phase solution; and
(e) heating said combined aqueous phase solutions to an effective temperature to reduce the amount of monofluoroacetate in said combined aqueous phase solutions, wherein fluoride concentration in said combined aqueous phase solutions is substantially high.
22. The process of claim 21 wherein said first batch of hydrofluorocarbon is the same as said second batch of hydrofluorocarbon.