Fluorine removal from antimony fluorohalide catalyst using chlorocarbons
US-2024173700-A1 · May 30, 2024 · US
US10166538B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10166538-B2 |
| Application number | US-201414763874-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 20, 2014 |
| Priority date | Jan 29, 2013 |
| Publication date | Jan 1, 2019 |
| Grant date | Jan 1, 2019 |
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A fluorination catalyst such as a chromium oxide-based fluorination catalyst may be activated or reactivated by contacting the catalyst. with a source of reactive fluorine, for example nitrogen trifluoride (NF3) or fluorine (F2). Fluorinated compounds may be prepared by the gas phase reaction of hydrogen fluoride (HF) with various substrates such as chlorinated compounds. A number of metal oxide-based catalysts have been developed for this purpose.
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What is claimed is: 1. A method of reactivating a spent or depleted chromium oxide-based fluorination catalyst, comprising contacting the spent or depleted chromium oxide-based fluorination catalyst with an agent that is a source of reactive fluorine selected from the group consisting of interhalogens, hypofluorites, fluorinated peroxides, OF 2 , O 2 F 2 , N 2 F 2 , N 2 F 4 , SOF 4 , SOF 2 , XeF 2 , XeF 4 , XeF 6 , KrF 2 , FNO, FNO 2 , FClO 3 , and mixtures thereof. 2. The method of claim 1 , wherein the chromium oxide-based fluorination catalyst is a bulk (unsupported) or supported chromium oxide-based fluorination catalyst. 3. The method of claim 1 , wherein the fluorination catalyst has been used to catalyze the fluorination of a chloroolefin or chloroalkane using HF. 4. The method of claim 1 , wherein the contacting is carried in a gas phase at a temperature of about 330° C. to about 400° C. 5. A method of activating a chromium oxide-based fluorination catalyst, comprising contacting a chromium oxide-based fluorination catalyst precursor with an agent that is a source of reactive fluorine selected from the group consisting of interhalogens, hypofluorites, fluorinated peroxides, OF 2 , O 2 F 2 , N 2 F 2 , N 2 F 4 , SOF 4 , SOF 2 , XeF 2 , XeF 4 , XeF 6 , KrF 2 , FNO, FNO 2 , FClO 3 , and mixtures thereof. 6. The method of claim 5 , wherein the chromium oxide-based fluorination catalyst precursor is comprised of bulk (unsupported) or supported chromium oxide. 7. The method of claim 5 , wherein the contacting is carried in a gas phase at a temperature of about 300° C. to about 400° C. 8. A fluorination process, alternately comprising reaction stages and regeneration stages, wherein the reaction stages comprise reacting a compound with HF in gas phase in the presence of a chromium oxide-based fluorination catalyst to produce a fluorinated compound and the regeneration stages comprise contacting the fluorination catalyst with an agent that is a source of reactive fluorine selected from the group consisting of interhalogens, hypofluorites, fluorinated peroxides, OF 2 , O 2 F 2 , N 2 F 2 , N 2 F 4 , SF 4 , SOF 4 , SOF 2 , XeF 2 , XeF 4 , XeF 6 , KrF 2 , FNO, FNO 2 , FClO 3 , and mixtures thereof. 9. The fluorination process of claim 8 , wherein the chromium oxide-based fluorination catalyst is a bulk (unsupported) or supported chromium oxide-based fluorination catalyst. 10. The fluorination process of claim 8 , additionally comprising a preliminary activation stage which comprises contacting a fluorination catalyst precursor with an agent that is a source of reactive fluorine.
fluorine-containing · CPC title
with simultaneous increase of the number of halogen atoms · CPC title
Chromium · CPC title
Manganese · CPC title
with chromium, molybdenum, tungsten or polonium · CPC title
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