Process for the manufacture of 2-chloro-3,3,3-trifluoropropene by gas phase fluorination of pentachloropropane
US-9284240-B2 · Mar 15, 2016 · US
US10414704B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10414704-B2 |
| Application number | US-201615014583-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 3, 2016 |
| Priority date | Oct 22, 2010 |
| Publication date | Sep 17, 2019 |
| Grant date | Sep 17, 2019 |
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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-chloro-3,3,3-trifluoropropene in presence of a catalyst and oxygen.
Opening claim text (preview).
The invention claimed is: 1. A catalytic fluorination process for producing 2-chloro-3,3,3-trifluoropropene comprising: activating a fluorination catalyst with a fluorine-containing compound, wherein the fluorination catalyst is a chromium catalyst further comprising a zinc co-catalyst, said zinc co-catalyst being present in an amount from about 1-10 wt % of said fluorination catalyst, and reacting 1,1,1,2,3-pentachloropropane and/or 1,1,2,2,3-pentachloropropane in a gas phase in the presence of HF, oxygen, and the activated fluorination catalyst and the absence of a polymerization stabilizer, wherein the fluorination reaction takes place at a reaction pressure and activating the fluorination catalyst takes place at a pressure above the reaction pressure. 2. The process according to claim 1 , wherein the ratio of oxygen with respect to 1,1,1,2,3-pentachloropropane and/or 1,1,2,2,3-pentachloropropane is 0.05 to 15 mole %. 3. The process according to claim 1 , wherein said catalyst is supported on a support selected from the group consisting of fluorinated alumina, fluorinated chromia, fluorinated activated carbon and graphite carbon. 4. The process according to claim 1 , wherein the 1,1,1,2,3-pentachloropropane contains up to 40 mol % of isomer 1,1,2,2,3-pentachloropropane. 5. The process according to claim 1 , wherein the process is carried out at a temperature of from 200 to 450° C. 6. The process according to claim 1 , wherein the process is carried out with a contact time from 6 to 100 sec. 7. The process according to claim 1 , wherein the process is carried out with a molar ratio HF:240 from 3:1 to 150:1. 8. The process according to claim 1 wherein the process is continuous.
Use of additives, e.g. for stabilisation · CPC title
the other compound being HX · CPC title
Nickel and chromium · CPC title
by splitting-off hydrogen halides from halogenated hydrocarbons · CPC title
containing fluorine · CPC title
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