IP Library Granted Patent US 8,884,083
Granted Patent B2
US 8,884,083 · App. 13/370,397 · Granted Nov 11, 2014

Selective catalytical dehydrochlorination of hydrochlorofluorocarbons

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,884,083
App. No.
13/370,397
Granted
Nov 11, 2014
Kind
B2
Abstract

A dehydrochlorination process is disclosed. The process involves contacting R f CHClCH 2 Cl with a catalyst in a reaction zone to produce a product mixture comprising R f CCl═CH 2 , wherein said catalyst comprises MY supported on carbon, and wherein R f is a perfluorinated alkyl group, M=K, Na or Cs, and Y=F, Cl or Br.

Claims (22)

1. A dehydrochlorination process comprising contacting R f CHClCH 2 Cl with a catalyst in a reaction zone to produce a product mixture comprising R f CCl═CH 2 , wherein said catalyst comprises an alkali metal halide salt of the formula MY supported on carbon, and wherein R f is a perfluorniated alkyl group, M=K, Na or Cs, and Y=F, Cl or Br and wherein the catalyst contains from about 5wt % to about 40wt % alkali metal halide salt based on the total amount of alkali metal halide salt and carbon.

2. The dehydrochlorination process of claim 1 wherein the carbon is an activated carbon.

3. The dehydrochlorination process of claim 2 wherein the carbon is an acid washed activated carbon.

4. The dehydrochlorination process of claim 1 wherein M is K and Y is F or Cl.

5. The dehydrochlorination process of claim 1 wherein the temperature in the reaction zone is from about 140° C. to about 400° C.

6. The dehydrochlorination process of claim 5 wherein the temperature in the reaction zone is from about 150° C. to about 250° C.

7. The dehydrochlorination process of claim 6 wherein the temperature in the reaction zone is from about 175° C. to about 225° C.

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

9. The dehydrochlorination process of claim 1 wherein the product selectivity to R f CCl═CH 2 is at least 96 mole %.

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

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

12. The dehydrochlorination process according to claim 1 wherein the catalyst contains from about 10 wt % to about 30 wt % alkali metal halide salt based on the total amount of alkali metal halide salt and carbon.

13. A dehydrochlorination process comprising contacting R f CHClCH 2 Cl with a catalyst in a reaction zone to produce a product mixture comprising R f CCl═CH 2 , wherein said catalyst comprises MY supported on carbon, and wherein R f is a perfluorniated alkyl group, M=K, Na or Cs, and Y=F, Cl or Br, wherein the product selectivity to R f CCl═CH 2 is at least 90 mole %.

14. The dehydrochlorination process of claim 13 wherein the carbon is an activated carbon.

15. The dehydrochlorination process of claim 14 wherein the carbon is an acid washed activated carbon.

16. The dehydrochlorination process of claim 13 wherein M is K and Y is F or Cl.

17. The dehydrochlorination process of claim 13 wherein the temperature in the reaction zone is from about 140° C. to about 400° C.

18. The dehydrochlorination process of claim 17 wherein the temperature in the reaction zone is from about 150° C. to about 250° C.

19. The dehydrochlorination process of claim 18 wherein the temperature in the reaction zone is from about 175° C. to about 225° C.

20. The dehydrochlorination process of claim 13 wherein the product selectivity to R f CCl═CH 2 is at least 96 mole %.

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

22. The dehydrochlorination process of claim 13 wherein R f is CF 3 .

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Apr 4, 2018
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
To: THE CHEMOURS COMPANY FC, LLC
Reel/Frame 045845/0913 →
SECURITY INTEREST Recorded Apr 4, 2018
From: THE CHEMOURS COMPANY FC, LLC
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 045846/0011 →
SECURITY AGREEMENT Recorded Jun 10, 2015
From: THE CHEMOURS COMPANY FC LLC; THE CHEMOURS COMPANY TT, LLC
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 035839/0675 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2015
From: E. I. DU PONT DE NEMOURS AND COMPANY
To: THE CHEMOURS COMPANY FC, LLC
Reel/Frame 035432/0023 →