IP Library › Granted Patent US 12,630,690
Granted Patent B2
US 12,630,690 · App. 17/989,960 · Granted May 19, 2026

Recycling of plastics by solvent-targeted recovery and precipitation (STRAP)

Inventors: George W. Huber (Middleton, WI); Kevin L. Sánchez-Rivera (Madison, WI); Reid C Van Lehn (Madison, WI); Ted Walker (Madison, WI); Panzheng Zhou (Madison, WI)
Assignee: Wisconsin Alumni Research Foundation
C08J11/08C08J2323/06C08J2323/08C08J2323/12C08J2327/06C08J2329/04C08J2367/02C08J2377/02C08J2377/06
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Quick Facts
Patent No.
US 12,630,690
App. No.
17/989,960
Granted
May 19, 2026
Kind
B2
Abstract

Disclosed herein is a method to recover constituent polymers in multilayer plastic films or mixed plastic wastes. The method comprises selectively dissolving a polymer in a solvent at a temperature, wherein the polymer is soluble, but other polymers in the multilayer plastic film or mixed plastic waste are not. The solubilized polymer is then separated from the multilayer plastic film or mixed plastic waste by mechanical filtration and precipitated by changing the temperature and/or adding a cosolvent. The process is repeated for each of the polymer component, resulting in a number of segregated streams that can then be recycled. Computational tools can be used to select solvent systems and temperatures that selectively dissolve different polymers from among all of the components.

Claims (33)

1 . A method to recover constituent polymers in a multilayer plastic film or mixed plastic waste, comprising:

(a) selectively dissolving one or more polymers in a solvent at a temperature, wherein the one or more polymers are soluble, but other polymers in the multilayer plastic film or mixed plastic waste are not, to yield a solubilized polymer fraction;

(b) mechanically separating the solubilized polymer fraction from the multilayer plastic film or mixed plastic waste;

(c) precipitating each polymer of the solubilized polymer fraction from the solvent; and

(d) repeating steps (a), (b), and (c) for each different additional polymers in the multilayer plastic film or mixed plastic waste using a solvent and a temperature that selectively dissolves one or more of the additional polymers, wherein a different solvent is used for each step (a).

2 . The method of claim 1 , further comprising using computational tools to select the solvent and the temperature that selectively dissolves the one or more polymers from among all of the components present in the multilayer plastic film or mixed plastic waste.

3 . The method of claim 2 , wherein the computational tools include calculating Hansen solubility parameters (HSPs), molecular dynamics (MD) simulations, and combined quantum chemical and statistical mechanical modeling.

4 . The method of claim 1 , further comprising a deinking step to remove ink from the multilayer plastic film or mixed plastic waste before step (a).

5 . The method of claim 4 , wherein the deinking step is conducted by treating the multilayer plastic film or mixed plastic waste in a solvent comprising tetrahydrofuran (THF) and N,N-dimethylformamide (DMF).

6 . The method of claim 1 , further comprising cutting the multilayer plastic film or mixed plastic waste into stamps ≤1 cm 2 before step (a).

7 . The method of claim 1 , further comprising shredding the multilayer plastic film or mixed plastic waste into strips ≤5 mm, ≤4 mm, ≤3 mm, or ≤2 mm before step (a).

8 . The method of claim 1 , wherein in step (c), at least one polymer of the solubilized polymer fraction is precipitated from the solvent by adding an antisolvent.

9 . The method of claim 1 , wherein in step (c), at least one polymer of the solubilized polymer fraction is precipitated from the solvent by changing the temperature of the solvent.

10 . The method of claim 1 , wherein the multilayer plastic film consists essentially of polyethylene (PE), ethylene vinyl alcohol (EVOH) and polyethylene terephthalate (PET).

11 . The method of claim 10 , wherein in step (a), the PE is selectively dissolved in toluene, and the EVOH is selectively dissolved in dimethyl sulfoxide (DMSO).

12 . The method of claim 11 , wherein in step (c), the solubilized PE is precipitated by adding acetone, and the solubilized EVOH is precipitated by adding water.

13 . The method of claim 10 , wherein in step (a), the PE is selectively dissolved in toluene or a C 6 to C 12 alkane, and the EVOH is selectively dissolved in a solvent comprising DMSO and water.

14 . The method of claim 13 , wherein in step (c), the solubilized PE is precipitated by lowering the temperature of the toluene, and the solubilized EVOH is precipitated by lowering the temperature of the DMSO and water.

15 . The method of claim 10 , wherein the multilayer plastic film further comprises a tie layer comprising ethylene vinyl acetate (EVA).

16 . The method of claim 15 , wherein the EVA is dissolved in toluene in step (a) and precipitated by adding acetone in step (c) together with the PE, and the EVA is separated from the PE after step (c) by selectively dissolving the EVA in N-methylpyrrolidinone (NMP).

17 . The method of claim 15 , wherein the EVA is dissolved in toluene in step (a) together with the PE, and the EVA is separated from the PE in step (c) by lowering the temperature of the toluene to precipitate the PE.

18 . The method of claim 1 , wherein the multilayer plastic film consists essentially of polyethylene terephthalate glycol (PETG), PE, EVOH and PET.

19 . The method of claim 18 , wherein in step (a), the PETG is selectively dissolved in a solvent comprising DMF and THF, the PE is selectively dissolved in toluene, and the EVOH is selectively dissolved in a solvent comprising DMSO and water.

20 . The method of claim 19 , wherein in step (c), the solubilized PETG is precipitated by adding 1-propanol, the solubilized PE is precipitated by lowering the temperature of the toluene, and the solubilized EVOH is precipitated by lowering the temperature of the DMSO and water.

21 . The method of claim 1 , wherein the mixed plastic waste consists essentially of PE, polypropylene (PP), polyvinyl chloride (PVC), PET and polyamide (PA).

22 . The method of claim 21 , wherein in step (a), the PE is selectively dissolved in dodecane, and the PP is selectively dissolved in toluene.

23 . The method of claim 22 , wherein in step (c), the solubilized PE is precipitated by lowering the temperature of the dodecane, and the solubilized PP is precipitated by lowering the temperature of the toluene.

24 . The method of claim 1 , wherein the multilayer plastic film consists essentially of PE, EVOH and nylon.

25 . The method of claim 24 , wherein in step (a), the PE is selectively dissolved in toluene, and the EVOH is selectively dissolved in a solvent comprising DMSO and water.

26 . The method of claim 25 , wherein in step (c), the solubilized PE is precipitated by lowering the temperature of the toluene, and the solubilized EVOH is precipitated by lowering the temperature of the DMSO and water.

27 . The method of claim 1 , wherein the mixed plastic waste consists essentially of PVC, low-density polyethylene (LDPE), PP, high-density polyethylene (HDPE), PET, nylon 6,6,6, nylon 6, and nylon 6,6.

28 . The method of claim 27 , wherein in step (a), the PVC is selectively dissolved in THF, the LDPE is selectively dissolved in a C 6 to C 12 alkane, the PP is selectively dissolved in tetrahydropyran (THP) at about 90° C., the HDPE is selectively dissolved in toluene, the PET is selectively dissolved in γ-valerolactone (GVL) at about 160° C., the nylon 6,6,6 is selectively dissolved in 1,2-propanediol at about 135° C., the nylon 6 is selectively dissolved in DMSO at about 145° C., and the nylon 6,6 is selectively dissolved in formic acid at about 65° C.

29 . The method of claim 28 , wherein in step (c), the solubilized PVC is precipitated by adding water, the solubilized LDPE is precipitated by lowering the temperature of the C 6 to C 12 alkane, the solubilized PP is precipitated by lowering the temperature of the THP, the solubilized HDPE is precipitated by lowering the temperature of the toluene, the solubilized PET is precipitated by lowering the temperature of the GVL, the solubilized nylon 6,6,6 is precipitated by lowering the temperature of the 1,2-propanediol, the solubilized nylon 6 is precipitated by lowering the temperature of the DMSO, and the solubilized nylon 6,6 is precipitated by adding water.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2023
From: HUBER, GEORGE; SANCHEZ-RIVERA, KEVIN; VAN LEHN, REID; ZHOU, PANZHENG; WALKER, THEODORE
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 063415/0366 →
CONFIRMATORY LICENSE Recorded Dec 15, 2022
From: UNIVERSITY OF WISCONSIN-MADISON
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 062136/0654 →
Continuity (2)
Provisional Application 63280669 · Nov 18, 2021
Related Publication 20230174736A1 · Jun 8, 2023
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