IP Library Granted Patent US 11,795,291
Granted Patent B2
US 11,795,291 · App. 17/529,643 · Granted Oct 24, 2023

Process for the depolymerization of polyethylene terephthalate (PET)

Inventors: Adel Essaddam (Terrebonne, CA); Fares Essaddam (Terrebonne, CA)
Assignee: 9449710 CANADA INC.
C08J11/24C08J2367/02
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Quick Facts
Patent No.
US 11,795,291
App. No.
17/529,643
Granted
Oct 24, 2023
Kind
B2
Abstract

The present disclosure relates to the formation of dimethyl terephthalate (DMT) and mono ethylene glycol (MEG). The present invention also relates to the depolymerization of polyethylene terephthalate (PET) and the recovery of dimethyl terephthalate (DMT) and mono ethylene glycol (MEG) using sodium methoxide as a catalyst.

Claims (24)

1. A process for depolymerization of polyester comprised in a feedstock to form a terephthalate; the process comprising:

(i) mixing the feedstock comprising the polyester with a first portion of methanol to form a first mixture;

(ii) subsequent to (i), adding a methoxide to the first mixture;

(iii) admixing; and

(iv) subsequent to (iii), adding a second portion of methanol to the first mixture to form a second mixture, such that the methoxide concentration in the second mixture is maintained between about 0.2 wt % and about 5 wt %; thereby forming the terephthalate.

2. The process of claim 1 , wherein adding the second portion of methanol to the first mixture is performed continuously.

3. The process of claim 1 , wherein the polyester is selected from the group consisting of polyethylene terephthalate, polytrimethylene terephthalate, and polybutylene terephthalate.

4. The process of claim 1 , wherein the terephthalate is dimethyl terephthalate.

5. The process of claim 1 , wherein the methoxide is sodium methoxide.

6. The process of claim 1 , wherein the process further forms a glycol.

7. The process of claim 6 , wherein the glycol is mono ethylene glycol.

8. The process of claim 6 , wherein the glycol is obtained in at least about 80 mol % yield.

9. The process of claim 6 , wherein the glycol is obtained in at least about 85 mol % yield.

10. The process of claim 6 , wherein the glycol is obtained in at least about 90 mol % yield.

11. The process of claim 1 , wherein the methoxide concentration in the second mixture is maintained between about 0.2 wt % and about 3 wt %.

12. The process of claim 1 , wherein the methoxide concentration in the second mixture is maintained between about 0.2 wt % and about 2 wt %.

13. The process of claim 1 , wherein the terephthalate is obtained in at least about 90 mol % yield.

14. The process of claim 1 , wherein the terephthalate is obtained in at least about 95 mol % yield.

15. The process of claim 1 , wherein the terephthalate is obtained in at least about 99 mol % yield.

16. The process of claim 1 , wherein the amount of the first portion of methanol is between about 0.1 and about 0.5 kg/kg of the feedstock.

17. The process of claim 1 , wherein the amount of the first portion of methanol is between about 0.2 and about 0.4 kg/kg of the feedstock.

18. The process of claim 1 , wherein the amount of the first portion of methanol is about 0.3 kg/kg of the feedstock.

19. The process of claim 1 , wherein step (i) is conducted for about 15 mins to about 120 mins.

20. The process of claim 1 , wherein step (i) is conducted at a temperature between about 50° C. and about 100° C.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2022
From: ESSADDAM, ADEL; ESSADDAM, FARES
To: 9449710 CANADA INC.
Reel/Frame 059261/0708 →
Continuity (3)
Continuation 16821870 · Mar 17, 2020
Provisional Application 62821270 · Mar 20, 2019
Related Publication 20220135761A1 · May 5, 2022
Cited By (1)
US 12,415,901