IP Library Granted Patent US 12,110,444
Granted Patent B2
US 12,110,444 · App. 18/506,244 · Granted Oct 8, 2024

1,2,3,3,3-pentafluropropene production processes

Inventors: Velliyur Nott Mallikarjuna Rao (Wilmington, DE); Mario Joseph Nappa (Leesburg, FL); Allen Capron Sievert (Elkton, MD)
Assignee: THE CHEMOURS COMPANY FC, LLC
C09K5/045C07C17/00C07C17/087C07C17/206C07C17/23C07C17/354C07C17/383C07C19/08C07C19/10
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Quick Facts
Patent No.
US 12,110,444
App. No.
18/506,244
Granted
Oct 8, 2024
Kind
B2
Abstract

A process is disclosed for making CF 3 CF═CHF. The process involves reacting CF 3 CClFCCl 2 F with H 2 in a reaction zone in the presence of a catalyst to produce a product mixture comprising CF 3 CF═CHF. The catalyst has a catalytically effective amount of palladium supported on a support selected from the group consisting of alumina, fluorided alumina, aluminum fluoride and mixtures thereof and the mole ratio of H 2 to CF 3 CClFCCl 2 F fed to the reaction zone is between about 1:1 and about 5:1. Also disclosed are azeotropic compositions of CF 3 CClFCCl 2 F and HF and azeotropic composition of CF 3 CHFCH 2 F and HF.

Claims (12)

1. A process comprising distilling a composition of 1,2,3,3,3-pentafluoropropene (HFO-1225ye), CFO-1215yb, and HFO-1234yf, and optionally one or more members selected from HFO-1243zf, HFC-245eb, HCFC-244eb, HCFC-226ea, HCFC-235bb and HFC-263fb; and isolating HFO-1225ye.

2. The process of claim 1 wherein the HFO-1225ye comprises HFO-E-1225ye and HFO-Z-1225ye.

3. The process of claim 2 wherein the HFO-E-1225ye is present in an amount greater than HFO-Z-1225ye.

4. The process of claim 2 wherein the HFO-E-1225ye is present in an amount less than HFO-Z-1225ye.

5. The process of claim 1 wherein isolating HFO-1225ye comprising isolating HFO-E-1225ye or HFO-Z-1225ye.

6. The process of claim 1 wherein isolating HFO-1225ye comprising isolating HFO-E-1225ye and HFO-Z-1225ye.

7. The process of claim 1 further comprising recovering HFO-1225ye.

8. The process of any of claims 2-4 further comprising recovering at least one of HFO-E-1225ye and HFO-Z-1225ye.

9. A process comprising obtaining an isolated HFO-1225ye composition from a distillation column in which a composition of 1,2,3,3,3-pentafluoropropene (HFO-1225ye), CFO-1215yb, and HFO-1234yf, and optionally one or more members selected from HFO-1243zf, HFC-245eb, HCFC-244eb, HCFC-226ea, HCFC-235bb and HFC-263fb is distilled and using the isolated HFO-1225ye as a refrigerant.

10. The process of claim 9 wherein the HFO-1225ye comprises HFO-E-1225ye and HFO-Z-1225ye and the HFO-E-1225ye is present in an amount greater than HFO-Z-1225ye.

11. The process of claim 9 wherein the HFO-1225ye comprises HFO-E-1225ye and HFO-Z-1225ye and the HFO-E-1225ye is present in an amount less than HFO-Z-1225ye.

12. A process comprising obtaining isolated HFO-1225ye from a distillation column in which a composition of 1,2,3,3,3-pentafluoropropene (HFO-1225ye), CFO-1215yb, and HFO-1234yf, and optionally one or more members selected from HFO-1243zf, HFC-245eb, HCFC-244eb, HCFC-226ea, HCFC-235bb and HFC-263fb, is distilled.

Assignments (1)
SECURITY INTEREST Recorded May 7, 2024
From: THE CHEMOURS COMPANY FC, LLC
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 067341/0844 →
Continuity (8)
Continuation 18206127 · Jun 6, 2023
Continuation 17336575 · Jun 2, 2021
Continuation 16458350 · Jul 1, 2019
Continuation 14050636 · Oct 10, 2013
Division 13539963 · Jul 2, 2012
Division 12301065
Provisional Application 60816649 · Jun 27, 2006
Related Publication 20240076536A1 · Mar 7, 2024