IP Library Granted Patent US 10,808,084
Granted Patent B2
US 10,808,084 · App. 15/712,997 · Granted Oct 20, 2020

Methods for making renewable and chemically recyclable crosslinked polyester elastomers

Inventors: Jacob Paul Brutman (Red Bank, NJ); Deborah Kay Schneiderman (Chicago, IL); Marc Andrew Hillmyer (Minneapolis, MN); Guilhem Xavier De Hoe (Minneapolis, MN)
Assignee: Regents of the University of Minnesota
C08J3/24C08J11/24C08K3/013C08K3/36C08K9/00C08J2367/04C08K3/04C08K3/22C08K3/26Y02W30/706
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Quick Facts
Patent No.
US 10,808,084
App. No.
15/712,997
Granted
Oct 20, 2020
Kind
B2
Abstract

A method includes reacting a polymer derived from a lactone with a cyclic carbonate compound comprising 2 to 5 cyclic carbonate moieties and a catalyst to form a crosslinked polylactone elastomer.

Claims (15)

1. A method comprising reacting:

a polymer comprising a monomeric unit derived from a lactone selected from the group consisting of β-lactones, γ-lactones and δ-lactones; with

a cyclic carbonate compound comprising 2 to 5 cyclic carbonate moieties;

an initiator compound chosen from alcohols and aromatic polyols; and

a catalyst;

to form a crosslinked polylactone elastomer, wherein the polylactone elastomer comprises linear monomeric units derived from the initiator compound, linear monomeric units derived from the polymer, and branched monomeric units derived from the cyclic carbonate compound.

2. The method of claim 1 , wherein the lactone is alkyl-substituted.

3. The method of claim 1 , wherein the lactone is a valerolactone.

4. The method of claim 1 , wherein the cyclic carbonate compound comprises 2 cyclic carbonate moieties, and wherein the cyclic carbonate moieties comprise a ring with 4 to 6 members.

5. The method of claim 1 , wherein the cyclic carbonate ranges from 0.25 mol % to 2 mol % with respect to the amount of lactone in the reaction.

6. The method of claim 1 , wherein the catalyst comprises a guanidyl moiety.

7. The method of claim 6 , wherein the catalyst is a bicyclic compound.

8. The method of claim 1 , wherein the catalyst is present at about 0.1 mol % with respect to the amount of lactone in the reaction.

9. The method of claim 1 , further comprising reacting the crosslinked polylactone elastomer to convert hydroxyl end groups thereon to acetate groups, wherein the hydroxyl end groups on the polylactone elastomer are converted to acetate groups by exposing the elastomer to a reaction mixture comprising acetic anhydride and an amine.

10. The method of claim 1 , further comprising reacting the crosslinked polylactone elastomer with a polyol and a catalyst selected from the group consisting of Sn(II), Sn(IV), and combinations thereof, to depolymerize the polylactone and recover at least 90% of the lactone reactant.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 28, 2020
From: DE HOE, GUILHEM XAVIER
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 053905/0366 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2020
From: BRUTMAN, JACOB PAUL; SCHNEIDERMAN, DEBORAH KAY
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 053743/0217 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2020
From: HILLMYER, MARC ANDREW
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 051809/0156 →
CONFIRMATORY LICENSE Recorded Nov 15, 2017
From: UNIVERSITY OF MINNESOTA
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 044456/0506 →
Continuity (2)
Provisional Application 62398894 · Sep 23, 2016
Related Publication 20180100041A1 · Apr 12, 2018