IP Library Granted Patent US 12,201,970
Granted Patent B2
US 12,201,970 · App. 18/061,253 · Granted Jan 21, 2025

Selective catalytic dehydrochlorination of hydrochlorofluorocarbons

Inventor: Mario Joseph Nappa (Leesburg, FL)
Assignee: THE CHEMOURS COMPANY FC, LLC
B01J35/613B01J23/26B01J27/12B01J37/26C07C17/25C07C21/18B01J27/132C07C2527/12
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Quick Facts
Patent No.
US 12,201,970
App. No.
18/061,253
Granted
Jan 21, 2025
Kind
B2
Abstract

A dehydrochlorination process is disclosed. The process involves contacting R f CHClCH 2 Cl with a chromium oxyfluoride catalyst in a reaction zone to produce a product mixture comprising R f CCl═CH 2 , wherein R f is a perfluorinated alkyl group.

Claims (17)

1. A dehydrochlorination process comprising contacting R f CHClCH 2 Cl with a catalyst consisting of chromium oxyfluoride catalyst in a reaction zone at a temperature of about 200° C. to about 500° C. for a contact time of about 5 seconds to about 150 seconds to produce a product mixture comprising R f CCl═CH 2 , wherein R f is a perfluorination alkyl group.

2. The dehydrochlorination process of claim 1 , wherein the temperature is about 275° C. to about 450° C.

3. The dehydrochlorination process of claim 2 , wherein the temperature is about 300° C. to about 400° C.

4. The dehydrochlorination process of claim 1 , wherein the contact time is about 10 seconds to about 100 seconds.

5. The dehydrochlorination process of claim 1 further comprising feeding the R f CHClCH 2 Cl to a reactor containing the chromium oxyfluoride in the reaction zone.

6. The dehydrochlorination process of claim 5 further comprising feeding HF to the reactor.

7. The dehydrochlorination process of claim 6 , wherein a mole ratio of feeding HF to feeding R f CHClCH 2 Cl is about 5:1 to about 25:1.

8. The dehydrochlorination process of claim 6 , wherein a mole ratio of feeding HF to feeding R f CHClCH 2 Cl is about 0.9:1 or less.

9. The dehydrochlorination process of claim 5 further comprising feeding an inert gas to the reactor.

10. The dehydrochlorination process of claim 5 , wherein the reactor comprises a reactor tube.

11. The dehydrochlorination process of claim 1 , wherein R f is CF 3 .

12. The dehydrochlorination process of claim 1 , wherein the product selectivity to R f CCl═CH 2 is at least 90 mole %.

13. The dehydrochlorination process of claim 12 , wherein the product selectivity to R f CCl═CH 2 is at least 95 mole %.

14. The dehydrochlorination process of claim 1 , wherein the dehydrochlorination selectivity to R f CCl═CH 2 is at least 95 mole %.

15. The dehydrochlorination process of claim 14 , wherein the dehydrochlorination selectivity to R f CCl═CH 2 is at least 99 mole %.

16. The dehydrochlorination process of claim 1 , wherein the chromium oxyfluoride has the formula Cr 2 O x F y , wherein x+y/2=3.

17. The dehydrochlorination process of claim 1 , wherein the chromium oxyfluoride comprises an alkali metal content of about 2000 ppm or less and a surface area of from about 10 m 2 /g to about 800 m 2 /g.

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 →