Method for purifying fluid that includes trifluoroethylene, and method for producing trifluoroethylene
US-2016347693-A1 · Dec 1, 2016 · US
US9249072B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9249072-B2 |
| Application number | US-201214233868-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 18, 2012 |
| Priority date | Jul 19, 2011 |
| Publication date | Feb 2, 2016 |
| Grant date | Feb 2, 2016 |
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The invention provides a process comprising contacting (1243zf) or (253fb) with hydrogen in the presence of a hydrogenation catalyst to produce a composition comprising 1,1,1-trifluoropropane (263fb).
Opening claim text (preview).
The invention claimed is: 1. A process for the preparation of a composition comprising 1,1,1-trifluoropropane (263fb), comprising the step of: reacting one of 3,3,3-trifluoropropene (1243zf) or 3-chloro-1,1,1-trifluoropropane (253fb) with hydrogen in the presence of a catalyst and in the presence of 263fb to produce 1,1,1-trifluoropropane (263fb), wherein 263fb is introduced into the reaction vessel or zone in which the reaction is conducted before the start of the reacting step. 2. A process according to claim 1 , wherein said process is conducted in the vapor phase. 3. A process according to claim 1 , said process further comprising the steps of: (i) providing a mixture of 263fb and at least a portion of said 1243zf; and (ii) contacting said mixture with said hydrogen. 4. A process according to claim 1 , wherein said reacting step is carried out at a temperature of from about −25 to about 300° C. and a pressure of from about 0 to about 40 bara. 5. A process according to claim 2 , wherein the reacting step is carried out at a temperature of from about 0 to about 300° C. 6. A process according to claim 5 , wherein the reacting is carried out at a temperature of from about 20 to about 200° C. 7. A process according to claim 6 , wherein the reacting is carried out at a temperature of from about 50 to about 150° C. 8. A process according to claim 1 comprising reaction of 1243zf with said hydrogen, wherein the molar ratio of hydrogen: 1243zf is from about 1:1 to about 40:1. 9. A process according to claim 1 , comprising the reaction of 253fb with said hydrogen, wherein the molar ratio of hydrogen: 253fb is from about 1:1 to about 40:1. 10. A process according to claim 1 wherein said catalyst comprises one of a supported or unsupported transition metal selected from Ni, Pd, Pt, Re, Rh, Ru and mixtures thereof. 11. A process according to claim 10 , wherein said catalyst is supported on at least one of alumina, titania, silica, zirconia or fluorides of the foregoing, calcium fluoride, carbon or barium sulphate. 12. A process according to claim 10 , wherein said catalyst is (a) platinum supported on alumina Pt/Al2O3; or (b) chlorotris(triphenylphosphine)rhodium(I). 13. A process according to claim 1 , wherein said process is carried out in the liquid phase in a solvent comprising 263fb and in which said catalyst is chlorotris(triphenylphosphine)rhodium(I) (Wilkinson's catalyst).
by splitting-off hydrogen halides from halogenated hydrocarbons · CPC title
by dehalogenation · CPC title
by hydrogenation · CPC title
containing fluorine · CPC title
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