Process for the manufacture of 2,3,3,3-tetrafluoropropene by gas phase fluorination of pentachloropropane
US-9278895-B2 · Mar 8, 2016 · US
US9828315B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9828315-B2 |
| Application number | US-201715453992-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 9, 2017 |
| Priority date | Jan 21, 2011 |
| Publication date | Nov 28, 2017 |
| Grant date | Nov 28, 2017 |
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The present invention provides a process of catalytic fluorination in gas phase of product 1,1,1,2,3-pentachloropropane or/and 1,1,2,2,3-pentachloropropane into product 2,3,3,3-tetrafluoropropene in presence of a catalyst.
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The invention claimed is: 1. A process for producing 2,3,3,3-tetrafluoropropene (1234yf) comprising: introducing 1,1,1,2,3-pentachloropropane (240db) and/or 1,1,2,2,3-pentachloropropane (240aa), HF, and a first mixture comprising 1,1,1,2,2-pentafluoropropane (245cb), 2-chloro-3,3,3-trifluoropropene (1233xf) and 2,3,3,3-tetrafluoropropene (1234yf) into a gas phase fluorination reactor containing a fluorination catalyst, wherein at least a part of the 245cb introduced to the reactor is provided from a recycle loop, and (ii) producing 1234yf and 1233xf in the reactor, wherein 1234yf and recycled 245cb form an equilibrium in the reactor thus resulting in increased production of 1234yf and a constant rate of 245cb in the recycle loop. 2. The process of claim 1 , wherein the 1,1,1,2,3-pentachloropropane (240db) and/or 1,1,2,2,3-pentachloropropane (240aa), HF, and first mixture are introduced to the reactor under conditions sufficient to produce a reaction mixture comprising 2,3,3,3-tetrafluoropropene (1234yf), 2-chloro-3,3,3-trifluoro-1-propene (1233xf) and 1,1,1,2,2-pentafluoropropane (245cb), the process further comprising; (iii) separating the reaction mixture into a first stream comprising 2,3,3,3 tetrafluoropropene (1234yf) and a second stream comprising 2-chloro-3,3,3-trifluoro-1-propene (1233xf) and 1,1,1,2,2-pentafluoropropane (245cb); and (iv) recycling at least a part of the second stream back to step (i). 3. The process of claim 1 , wherein the process is carried out in a single stage. 4. The process of claim 1 , wherein the product 2,3,3,3-tetrafluoropropene is present at a concentration of at least 1%. 5. The process of claim 1 , wherein said catalyst is a chromium catalyst. 6. The process of claim 4 , wherein said catalyst further comprises a co-catalyst selected from the group consisting of Ni, Co, Zn, Mn, Mg and mixtures thereof, and wherein said co-catalyst is present in an amount from about 1-10 wt % of said fluorination catalyst. 7. The process of claim 1 , wherein the process is carried out in the presence of a catalyst comprising Ni—Cr. 8. The process of claim 1 , wherein said catalyst is supported on a support comprising fluorinated alumina, fluorinated chromia, fluorinated activated carbon or graphite carbon. 9. The process of claim 1 , wherein the fluorination catalyst is activated with a fluorine-containing compound. 10. The process of claim 1 , wherein the 1,1,1,2,3-pentachloropropane contains up to 40 mol % of isomer 1,1,2,2,3-pentachloropropane. 11. The process of claim 1 , wherein the process is carried out at a pressure from 3 to 20 bars. 12. The process of claim 1 , wherein the process carried out at a temperature of from 200 to 450° C. 13. The process of claim 11 , wherein the process carried out at a temperature of 350 to 450° C.
Nickel and chromium · CPC title
by distillation · CPC title
with scandium, yttrium, aluminium, gallium, indium or thallium · CPC title
by splitting-off hydrogen halides from halogenated hydrocarbons · CPC title
the other compound being HX · CPC title
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