Method for separating 1-chloro-3,3,3-trifluoropropene and hydrogen fluoride, and method for producing 1-chloro-3,3,3-trifluoropropene by using same
US-9221732-B2 · Dec 29, 2015 · US
US9567275B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9567275-B2 |
| Application number | US-201514876384-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 6, 2015 |
| Priority date | Oct 3, 2006 |
| Publication date | Feb 14, 2017 |
| Grant date | Feb 14, 2017 |
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The invention relates to a process for preparing a C3-6 (hydro)fluoroalkene comprising dehydrohalogenating a C3-6 hydro(halo)fluoroalkane in the presence of a zinc/chromia catalyst, wherein the C 3-6 (hydro)fluoroalkene produced is isomerized in the presence of the zinc/chromia catalyst.
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We claim: 1. A process for preparing 2,3,3,3-tetrafluoropropene (CF3CF═CH2) comprising: (i) fluorinating 3,3,3-trifluoro-2-chloropropene (CF3CCl═CH2) with HF in the vapour phase in the presence of a chromia-containing catalyst to produce an intermediate composition comprising 1,1,1,2-tetrafluoro-2-chloropropane (CF3CFClCH3) and 1,1,1,2,2-pentafluoropropane (CF 3 CF 2 CH 3 ); and (ii) dehydrochlorinating the CF3CFClCH3 in the intermediate composition to produce CF3CF═CH2. 2. A process according to claim 1 , wherein step (ii) is carried out in the presence of a zinc/chromia catalyst. 3. A process according to claim 2 , wherein the zinc/chromia catalyst comprises 0.01 to 25% by weight zinc. 4. A process according to claim 2 , wherein the zinc/chromia catalyst is amorphous or from 0.1 to 50% by weight of the catalyst is in the form of one or more crystalline compounds of chromium and/or one or more crystalline compounds of zinc. 5. A process according to claim 1 , wherein CF3CFClCH3 is fluorinated to produce CF3CF2CH3. 6. A process according to claim 5 , wherein CF3CFClClH3 is fluorinated with HF in the presence of a chromia-containing catalyst to produce CF3CF2CH3. 7. A process according to claim 1 , wherein the CF3CF2CH3 is dehydrofluorinated to produce CF3CF═CH2. 8. A process according to claim 1 , wherein the ratio of HF:organics in the fluorinating step is from about 5:1 to about 30:1. 9. A process according to claim 1 , wherein the process is carried out at a temperature of greater than 300° C. 10. A process according to claim 1 , wherein the process is carried out at super-atmospheric pressure. 11. A process according to claim 1 , wherein the process is carried out at a pressure in the range from 1 to 5 bara. 12. A process according to claim 1 , wherein the catalyst is subsequently regenerated. 13. A process according to claim 12 , wherein the regeneration step is oxidative regeneration. 14. A process according to claim 1 , wherein the process is carried out with a diluent gas. 15. A process according to claim 14 , wherein the diluent gas comprises nitrogen. 16. A process according to claim 1 , wherein dehydrochlorination is carried out in the presence of a feed comprising hydrogen fluoride (HF). 17. A process according to claim 1 , wherein the dehydrochlorination is carried out in the absence of added hydrogen fluoride.
to unsaturated halogenated hydrocarbons · CPC title
containing chlorine · CPC title
containing fluorine · CPC title
to unsaturated halogenated hydrocarbons · CPC title
and chlorine · CPC title
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