IP Library Granted Patent US 11,920,005
Granted Patent B2
US 11,920,005 · App. 17/246,204 · Granted Mar 5, 2024

Use of multifunctional CO2 for depolymerization of polyethylene terephthalate

Inventors: Maohong Fan (Ames, IA); Wenyang Lu (Laramie, WY); Jinwen Zhang (Pullman, WA)
Assignees: UNIVERSITY OF WYOMING; WASHINGTON STATE UNIVERSITY
C08J11/14B01J3/008B01J3/02C08J2367/02
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Quick Facts
Patent No.
US 11,920,005
App. No.
17/246,204
Granted
Mar 5, 2024
Kind
B2
Abstract

A high-efficiency, low-energy consumption and environmental-friendly recycling technology for PETE plastic waste is disclosed. The degradation of PETE plastic waste includes a method for attacking the —O— ester linkage in the repeat unit of PETE plastic with water in saturated pressure and CO 2 in supercritical (Sc) conditions.

Claims (15)

1. An environmentally friendly method for recycling polyethylene terephthalate (PETE), comprising:

pre-loading a supercritical high temperature reactor with a weight ratio of a polyethylene terephthalate and a deionized (DI) water in excess of 1:10;

injecting CO2 into the supercritical high temperature reactor at an injection pressure in excess of 500 psi;

sealing the weight ratio of the polyethylene terephthalate and the deionized water and the CO2 within the supercritical high temperature reactor;

setting a reaction temperature of the supercritical high temperature reactor with a controller, wherein the reaction temperature is in excess of 160° C.;

heating the weight ratio of the polyethylene terephthalate and the deionized water and the CO2 within the supercritical high temperature reactor to the reaction temperature; and

reacting the weight ratio of the polyethylene terephthalate and the deionized water and the CO2 within the reactor for a reaction duration in excess of 0.25 hrs.

2. The method of claim 1 , wherein the weight ratio of the polyethylene terephthalate and the deionized (DI) water is ≤1:30.

3. The method of claim 1 , wherein the reaction temperature is 240° C.

4. The method of claim 1 , wherein the reaction time is 2.0 hrs.

5. The method of claim 1 , further comprising:

collecting the CO2 after the completion of the reaction from the supercritical high temperature reactor.

6. The method of claim 1 , further comprising:

collecting a solid product reactant from the supercritical high temperature reactor, wherein the solid product reactant comprises polyenes and benzoic acid crystals; and

collecting a liquid product reactant from the supercritical high temperature reactor, wherein the liquid product reactant comprises ethylene glycol.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2021
From: FAN, MAOHONG; LU, WENYANG
To: UNIVERSITY OF WYOMING
Reel/Frame 056132/0805 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2021
From: ZHANG, JINWEN
To: WASHINGTON STATE UNIVERSITY
Reel/Frame 056132/0932 →
Continuity (2)
Provisional Application 63018189 · Apr 30, 2020
Related Publication 20210340351A1 · Nov 4, 2021