IP Library Granted Patent US 9,315,432
Granted Patent B2
US 9,315,432 · App. 14/486,143 · Granted Apr 19, 2016

Process for producing 2, 3, 3, 3-tetrafluoropropene and 1, 1-difluoroethylene

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 9,315,432
App. No.
14/486,143
Granted
Apr 19, 2016
Kind
B2
Abstract

To provide an economically advantageous process for producing HFO-1234yf useful as a new refrigerant in sufficiently high yield by one reaction involving thermal decomposition. A process for producing HFO-1234yf and VdF from raw material containing R22, R40 and TFE, by a synthetic reaction involving thermal decomposition, which comprises (a) a step of supplying the R22, the R40 and the TFE to a reactor, as preliminarily mixed or separately, (b) a step of supplying a heat medium to the reactor, and (c) a step of bringing the heat medium in contact with the R22, the R40 and the TFE in the reactor to form the HFO-1234yf and the VdF.

Claims (22)

1. A process for producing 2,3,3,3-tetrafluoropropene and 1,1-difluoroethylene from chlorodifluoromethane, chloromethane and tetrafluoroethylene, the process comprising:

(a) supplying chlorodifluoromethane, chloromethane and tetrafluoroethylene to a reactor, as preliminarily mixed or separately,

(b) supplying a heat medium to the reactor, and

(c) contacting the heat medium with chlorodifluoromethane, chloromethane and tetrafluoroethylene in the reactor to form a reaction product comprising 2,3,3,3-tetrafluoropropene and 1,1-difluoroethylene.

2. The process according to claim 1 , wherein a molar ratio of tetrafluoroethylene to chlorodifluoromethane supplied to the reactor ranges from 0.01 to 100.

3. The process according to claim 1 , wherein a molar ratio of chloromethane to chlorodifluoromethane and tetrafluoroethylene in total supplied to the reactor ranges from 0.1 to 10.

4. The process according to claim 1 , wherein chloromethane is supplied to the reactor at a temperature of from 0 to 1,200° C.

5. The process according to claim 1 , wherein chlorodifluoromethane is supplied to the reactor at a temperature of from 0 to 600° C.

6. The process according to claim 1 , wherein tetrafluoroethylene is supplied to the reactor at a temperature of from 0 to 1,200° C.

7. The process according to claim 1 , wherein a temperature in the reactor in said contacting (c) is adjusted to be from 400 to 1,200° C.

8. The process according to claim 1 , wherein the heat medium is supplied to the reactor at a temperature of from 100 to 1,200° C.

9. The process according to claim 1 , wherein the heat medium is at least one selected from the group consisting of steam, nitrogen and carbon dioxide.

10. The process according to claim 1 , wherein the heat medium is supplied at an amount of from 20 to 98 vol % in an entire gas supplied to the reactor.

11. The process according to claim 1 , wherein gas supplied to the reactor has a contact time in the reactor of from 0.01 to 10 seconds.

12. The process according to claim 1 , wherein a pressure in the reactor is from 0 to 2 MPa by gauge pressure.

13. The process according to claim 1 , wherein at least one selected from the group consisting of chlorotrifluoroethylene, trifluoroethylene, hexafluoropropene and octafluorocyclobutane, is further supplied to the reactor.

14. The process according to claim 1 , wherein

the reaction product further comprises chlorotrifluoroethylene, and

a molar ratio of 2,3,3,3-tetrafluoropropene to chlorotrifluoroethylene in the reaction product is ≧9.0.

15. The process according to claim 1 , further comprising:

(d) after said contacting (c), withdrawing from the reactor a reaction mixture comprising 2,3,3,3-tetrafluoropropene and 1,1-difluoroethylene formed in the reactor,

wherein said supplying (a), said supplying (b), and said withdrawing (d) are continuously carried out.

Assignments (2)
CHANGE OF NAME Recorded Aug 7, 2018
From: ASAHI GLASS COMPANY, LIMITED
To: AGC INC.
Reel/Frame 046730/0786 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2014
From: FURUTA, SHOJI; TAKEUCHI, YU
To: ASAHI GLASS COMPANY, LIMITED
Reel/Frame 033887/0638 →