Fluorine removal from antimony fluorohalide catalyst using chlorocarbons

US11904301B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11904301-B2
Application numberUS-201917273342-A
CountryUS
Kind codeB2
Filing dateSep 6, 2019
Priority dateSep 7, 2018
Publication dateFeb 20, 2024
Grant dateFeb 20, 2024

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A method of chlorinating a antimony fluorohalide catalyst is disclosed. In one embodiment the method comprises contacting an antimony fluorohalide catalyst that contains one or more fluorines with a regenerating agent chosen from 2-chloro-3,3,3-trifluoropropene (1233xf), 1,1,1,3-tetrachloropropane (250fb), 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb) and combinations of 1233xf, 250fb, and 244bb, under conditions effective to exchange at least one fluorine in the antimony fluorohalide catalyst with chlorine. The method can be used to regenerate spent antimony fluorohalide catalyst, for example regenerating SbCl 5 from SbF 5 .

First claim

Opening claim text (preview).

What is claimed is: 1. A method of chlorinating an antimony fluorohalide catalyst comprising: contacting an antimony fluorohalide catalyst that contains one or more fluorines with a regenerating agent chosen from 2-chloro-3,3,3-trifluoropropene (1233xf), 1,1,1,3-tetrachloropropane (250th), 2-chloro-1,1,1,2-tetrafluoropropane (244bb), and combinations of two or more of 1233xf, 250fb, and 244bb under conditions effective to exchange at least one fluorine in the antimony fluorohalide catalyst with chlorine. 2. The method of claim 1 wherein the regenerating agent comprises 1233xf. 3. The method of claim 1 wherein the regenerating agent comprises 250fb. 4. The method of claim 1 wherein the regenerating agent comprises 244bb. 5. The method of claim 1 wherein the antimony fluorohalide catalyst comprises at least one of (i) SbF n X 5-n , wherein n is an integer of 1 to 5, and X is a halogen other than fluorine; and (ii) as SbFD m X′ 3-m , wherein m is an integer of 1 to 3, and X′ is a halogen other than fluorine; or mixtures of (i) and (ii). 6. The method of claim 5 wherein the antimony fluorohalide catalyst comprises SbF n X 5-m , wherein n is an integer of 1 to 5, and X is chlorine and the product is a chlorine-containing catalyst. 7. The method of claim 5 wherein the antimony fluorohalide catalyst comprises SbF m X′ 3-m , wherein m is an integer of 1 to 3, and X′ is chlorine. 8. The method of claim 5 wherein the antimony fluorohalide catalyst comprises SbF 3 . 9. The method of claim 5 wherein the antimony fluorohalide catalyst comprises SbF n X 5-n , wherein n is an integer of 1 to 5, and X is chlorine and SbF m X′ 3-m , wherein m is an integer of 1 to 3, and X′ is chlorine. 10. The method of claim 5 wherein the antimony fluorohalide catalyst comprises SbF 5 , SbF 4 Cl, SbF 3 Cl 2 , or mixtures thereof. 11. The method of claim 5 wherein the antimony fluorohalide catalyst comprises SbF 4 Cl and SbF 3 Cl 2 . 12. The method of claim 1 wherein the contacting occurs at a temperature between about 80° C. and about 120° C. 13. The method of claim 1 wherein the molar ratio of the regenerating agent to the antimony fluorohalide catalyst to the agent is between about 1 to about 5. 14. A method of regenerating and recovering a spent antimony fluorohalide catalyst to produce a chlorinated antimony catalyst comprising: (a) treating a spent antimony fluorohalide catalyst comprising (i) SbF n X 5-n , wherein n is an integer of 1 to 5, and X is a halogen other than fluorine, or (ii) SbF m X′ 3-m , wherein m is an integer of 1 to 3, and X′ is a halogen other than fluorine, or mixtures of (i) and (ii), with a regenerating agent chosen from 2-chloro-3,3,3-trifluoropropene (1233xf), 1,1,1,3-tetrachloropropane (250th), 2-chloro-1,1,1,2-tetrafluoropropane (244bb), and combinations of two or more of 1233xf, 250fb, and 244bb, under conditions effective to produce a chlorinated antimony catalyst; and (b) recovering the chlorinated antimony catalyst. 15. The method of claim 14 wherein the chlorinated antimony catalyst comprises SbC 5 . 16. The method of claim 14 wherein the chlorinated antimony catalyst comprises SbC 3 . 17. The method of claim 14 wherein the contacting occurs at a temperature between about 80° C. and about 120° C.; and the molar ratio of the regenerating agent to the spent antimony is between about 1 to about 5. 18. A composition comprising: at least one antimony fluorohalide catalyst selected from the group consisting of (i) SbF n X 5-n , wherein n is an integer of 1 to 5, and X is a halogen other than fluorine, and (ii) SbF m X′ 3-m , wherein m is an integer of 1 to 3, and X′ is a halogen other than fluorine, or mixtures of (i) and (ii); and at least one compound selected from the group consisting of 2-chloro-3,3,3-trifluoropropene (1233xf), 1,1,1,3-tetrachloropropane (250fb), 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb), and combinations of two or more of 1233xf, 250fb, and 244bb.

Assignees

Inventors

Classifications

  • B01J27/32Primary

    of catalysts comprising compounds of halogens · CPC title

  • B01J27/10Primary

    Chlorides · CPC title

  • of binary type SbX3 or SbX5 with X representing a halogen, or mixed of the type SbX3X'2 with X,X' representing different halogens · CPC title

  • B01J27/12Primary

    Fluorides · CPC title

  • fluorine-containing · CPC title

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What does patent US11904301B2 cover?
A method of chlorinating a antimony fluorohalide catalyst is disclosed. In one embodiment the method comprises contacting an antimony fluorohalide catalyst that contains one or more fluorines with a regenerating agent chosen from 2-chloro-3,3,3-trifluoropropene (1233xf), 1,1,1,3-tetrachloropropane (250fb), 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb) and combinations of 1233xf, 250fb, and 2…
Who is the assignee on this patent?
Chemours Co Fc Llc
What technology area does this patent fall under?
Primary CPC classification B01J27/32. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Feb 20 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 4 related publications on this page (citations in our corpus or others sharing the same primary CPC).