US2017313639A1PendingUtilityA1

Integrated process to produce 2,3,3,3-tetrafluoropropene

Assignee: HONEYWELL INT INCPriority: Mar 15, 2013Filed: Jul 20, 2017Published: Nov 2, 2017
Est. expiryMar 15, 2033(~6.6 yrs left)· nominal 20-yr term from priority
C07C 17/38C07C 17/25C07C 19/08C07C 19/10C07C 21/18C07C 17/386C07C 21/04C07C 19/01C07C 17/206C07C 17/087Y02P20/582Y02P20/125Y02P20/10
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Claims

Abstract

The invention relates to a separation process whereby 2-chloro-3,3,3-trifluoropropene (1233xf) is separated from a mixture containing other fluorinated organics and high boiling materials such as dimers using azeotropes of HF formed by adding appropriate amounts to the mixture which facilitate separation by, e.g. distillation.

Claims

exact text as granted — not AI-modified
1 - 20 . (canceled) 
     
     
         21 . An azeotrope composition comprising HF and at least one or more organics selected from the group consisting of trichlorofluoropropene (1231) isomers, 1,1,1,2,2-pentafluoropropane (245cb), dichlorotrifluoropropane (243) isomers, trichlorodifluorpropane (242) isomers, and 1,1,2,3-tetrachloropropene (1230xa). 
     
     
         22 . The azeotrope composition according to  claim 21  in which a 243 isomer is 2,3-dichloro-1,1,1-triflurorpropane (243db). 
     
     
         23 . The azeotrope composition of  claim 21  which is a binary or tertiary azeotrope. 
     
     
         24 . The azeotrope composition of  claim 21  wherein the HF-azeotrope is selected from the group consisting of 1230xa/HF and 243db/HF. 
     
     
         25 . The azeotrope composition of  claim 21  wherein the concentration of HF ranges from 5 to 95 wt %. 
     
     
         26 . The azeotrope composition of  claim 24  herein the concentration of HF ranges from 20 to 80 wt %. 
     
     
         27 . The azeotrope composition of  claim 25  wherein the concentration of HF ranges from 30 to 70 wt %. 
     
     
         28 . A composition comprising HF-azeotropes of 1233xf and at least one organic selected from trichlorofluoropropene (1231) isomers, 2,3-dichloro-3,3-difluoropropene (1232xf), 2-chloro-1,1,1,2,2-pentafluoropropane (245cb), dichlorotritluoropropane (243) isomers, and trichlorodifluorpropane (242) isomers. 
     
     
         29 . The composition of  claim 28  wherein the concentration of HF ranges from 5 to 95 wt %. 
     
     
         30 . The composition of  claim 29  wherein the concentration of HF ranges from 20 to 80 wt %. 
     
     
         31 . The composition of  claim 30  wherein the concentration of HF ranges from 30 to 70 wt. 
     
     
         32 . A composition comprising 2-chloro-3,3,3-trifluoropropene (1233xf) and at least one organic selected from trichiorofluoropropene (1231) isomers, 2,3-dichloro-3,3-difluoropropene (1232xt), 2-chloro-1,1,1,2-tetrafluoropropane (244bb), 1,1,1,2,2-pentafluoropropane (245cb), dichlorotrifluoropropane (243), and trichlorodifluorpropane (242), and one or more dimers selected from the group consisting of C 6 H 3 F 6 Cl, C 6 H 3 F 7 Cl 2 , C 6 F 6 Cl 2 , C 6 H 5 Cl 2 , C 6 F 5 Cl 3 , C 6 H 3 F 2 Cl 5 , and combinations thereof. 
     
     
         33 . The composition according to  claim 32  wherein HF is additionally present. 
     
     
         34 . The composition according to  claim 32  in which a 243 isomer is 2,3-dichloro-1,1,1-triflurorpropane (243db). 
     
     
         35 . A composition comprising one or more dimers selected from the group consisting of C 6 H 3 F 6 Cl, C 6 H 3 F 7 Cl 2 , C 6 F 6 Cl 2 , C 6 H 8 Cl 2 , C 6 F 5 Cl 3 , C 6 H 3 F 2 Cl 5 , and combinations thereof.

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