Shape-memory polymers and methods of making and use thereof

Patent metadata

Field	Value
Publication number	US-10647812-B2
Application number	US-201615579629-A
Country	US
Kind code	B2
Filing date	Jun 6, 2016
Priority date	Jun 5, 2015
Publication date	May 12, 2020
Grant date	May 12, 2020

Abstract

Described are shape-memory polymers that have a composite prepolymer crosslinked with a stoichiometric amount of a multifunctional crosslinker, the composite prepolymer having a branched or telechelic prepolymer having a low polydispersity reacted with a non-crystalline chain extender. Also described are methods of making shape-memory polymers by reacting a branched or telechelic prepolymer having a low polydispersity with a non-crystalline chain extender to form a composite prepolymer, and crosslinking a stoichiometric amount of a multifunctional crosslinker with the composite prepolymer, thereby forming the shape-memory polymer.

First claim

What is claimed is:

1. A shape-memory polymer consists essentially of: a composite prepolymer crosslinked with a stoichiometric amount of a multifunctional isocyanate crosslinker, said composite prepolymer comprising a branched or telechelic polycaprolactone prepolymer having a low polydispersity reacted with a non-crystalline polyol chain extender.

2. The shape-memory polymer of claim 1 , wherein the branched polycaprolactone prepolymer is present and comprises 3 or more branches.

3. The shape-memory polymer of claim 1 , wherein the branched polycaprolactone prepolymer is present and each branch of the branched polycaprolactone prepolymer is substantially the same molecular weight.

4. The shape-memory polymer of claim 1 , wherein the molecular weight of the branched polycaprolactone prepolymer or the telechelic polycaprolactone prepolymer is 6,000 g/mol or less, as determined by HNMR.

5. The shape-memory polymer of claim 1 , wherein the molecular weight of each branch of the branched polycaprolactone prepolymer or the telechelic polycaprolactone prepolymer is 2,000 g/mol or less, as determined by HNMR.

6. The shape-memory polymer of claim 1 , wherein the molecular weight of the non-crystalline polyol chain extender is from 50 g/mol to 1,200 g/mol.

7. The shape-memory polymer of claim 1 , wherein the composite prepolymer comprises hydroxyl end groups; wherein the molecular weight of the composite prepolymer is from 2,000 g/mol to 8,000 g/mol; wherein the composite prepolymer has a polydispersity index of from 1 to 2.0; or a combination thereof.

8. The shape-memory polymer of claim 1 , wherein the multifunctional isocyanate crosslinker comprises 2 reactive groups.

9. The shape-memory polymer of claim 1 , wherein the effective molecular weight between crosslinks of the shape-memory polymer is from 1,000 g/mol to 10,000 g/mol.

10. The shape-memory polymer of claim 1 , wherein the shape-memory polymer comprises a residue of a free radical scavenger.

11. The shape-memory polymer of claim 1 , wherein the shape-memory polymer has an elastic energy density of 1 MJ/m 3 or more; an energy storage efficiency of 50% or more; a strength of 1 MPa or more; a strain fixity of 65% or more; a stress free or unconstrained shape recovery ratio of 0.9 or more; a stress free or unstrained melting temperature of 40° C. or less as measured by differential scanning calorimetry; or a combination thereof.

12. A method of making the shape-memory polymer of claim 1 , comprising: reacting a branched or telechelic polycaprolactone prepolymer having a low polydispersity with a non-crystalline polyol chain extender to form a composite prepolymer, and crosslinking stoichiometric amount of a multifunctional isocyanate crosslinker with the composite prepolymer, thereby forming the shape-memory polymer.

13. The method of claim 12 , further comprising stretching the shape-memory polymer having an unstretched length to form a stretched shape-memory polymer having a post-stretched length.

14. The method of claim 13 , wherein the post-stretched length is from 100% to 600% longer than the unstretched length.

15. The method of claim 13 , further comprising heating the stretched shape-memory polymer to a temperature above the melting temperature of the stretched shape-memory polymer.

16. The method of claim 13 , wherein the unstretched shape memory polymer has a stress free or unstained melting temperature of from 35° C. to 50° C. as measured by differential scanning calorimetry; wherein the stretched shape-memory polymer has a melting temperature of 40° C. or less as measured by differential scanning calorimetry; or a combination thereof.

Assignees

• Univ Rochester

Inventors

• Anthamatten Mitchell
• Meng Yuan

Classifications

• G01R33/46

  NMR spectroscopy · CPC title

• C08G2280/00

  Compositions for creating shape memory · CPC title

• C08G63/912

  derived from hydroxycarboxylic acids · CPC title

• G01N25/4866

  by using a differential method · CPC title

• C08G63/08

  Lactones or lactides · CPC title