Composition comprising HF and 1,3,3,3-tetrafluoropropene
US-10029963-B2 · Jul 24, 2018 · US
US10590052B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10590052-B2 |
| Application number | US-201816018191-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 26, 2018 |
| Priority date | Dec 19, 2013 |
| Publication date | Mar 17, 2020 |
| Grant date | Mar 17, 2020 |
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A process for producing a main (hydro)halocarbon compound, including the formation of a mixture of compounds including hydrogen fluoride, Z-3,3,3-trifluoro-1-chloropropene and one or more other (hydro)halocarbon compounds, distillation of this mixture making it possible to collect, firstly, an azeotropic composition, and, secondly, at least one of the compounds of the mixture. The (hydro) halocarbon compounds are preferably selected among tetrachlorofluoropropanes, trichlorodifluoropropanes, dichlorotrifluoropropanes, chlorotetrafluoropropanes, pentafluoropropanes, dichlorodifluoropropenes, chlorotrifluoropropenes and tetrafluoropropenes.
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The invention claimed is: 1. A process for producing a (hydro)halocarbon compound comprising from 1 to 3 carbon atoms, comprising: forming a mixture of compounds comprising hydrogen fluoride, Z-3,3,3-trifluoro-1-chloropropene and two or more (hydro)halocarbon compounds comprising from 1 to 3 carbon atoms; distilling the mixture to, firstly, an azeotropic composition comprising hydrogen fluoride, Z-3,3,3-trifluoro-1-chloropropene and two or more (hydro)halocarbon compounds comprising from 1 to 3 carbon atoms, and, secondly, at least one of the compounds of the mixture. 2. The process as claimed in claim 1 , comprising distilling the mixture to collect, firstly, the azeotropic composition, and, secondly, hydrogen fluoride. 3. The process as claimed in claim 1 , comprising distilling the mixture to collect, firstly, the azeotropic composition, and, secondly, E-3,3,3-trifluoro-1-chloropropene. 4. The process as claimed in claim 1 , wherein the at least one of the compounds of the mixture comprises 3,3,3-trifluoro-1-chloropropene. 5. The process as claimed in claim 1 , wherein the at least one of the compounds of the mixture comprises E-3,3,3-trifluoro-1-chloropropene. 6. The process as claimed in claim 1 , wherein the forming the mixture of compounds comprises a fluorination step, comprising the reaction of a chloro compound with hydrogen fluoride. 7. The process as claimed in claim 6 , comprising separating the azeotropic composition into two immiscible liquid fractions, namely a fraction rich in hydrogen fluoride and a fraction poor in hydrogen fluoride, the fraction rich in hydrogen fluoride containing a higher proportion of hydrogen fluoride than the fraction poor in hydrogen fluoride; and the fraction rich in hydrogen fluoride being, where appropriate, recycled into the fluorination step. 8. The process as claimed in claim 7 , comprising separating the azeotropic composition by decantation. 9. The process as claimed in claim 6 , wherein the chloro compound is 1,1,1,3,3-pentachloropropane or 1,1,3,3-tetrachloropropene. 10. The process as claimed in claim 1 , wherein the two or more (hydro)halocarbon compounds comprise three carbon atoms. 11. The process as claimed in claim 1 , wherein the two or more (hydro)halocarbon compounds is selected from the group consisting of tetrachlorofluoropropanes, trichlorodifluoropropanes, dichlorotrifluoropropanes, chlorotetrafluoropropanes, pentafluoropropanes, dichlorodifluoropropenes, trichlorofluoropropenes, chlorotrifluoropropenes and tetrafluoropropenes.
containing fluorine · CPC title
by distillation · CPC title
Geometrical isomers · CPC title
Azeotropic distillation · CPC title
containing fluorine · CPC title
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