Bio-inspired method to obtain multifunctional dynamic nanocomposites

Patent metadata

Field	Value
Publication number	US-9938368-B2
Application number	US-201314383038-A
Country	US
Kind code	B2
Filing date	Mar 7, 2013
Priority date	Mar 7, 2012
Publication date	Apr 10, 2018
Grant date	Apr 10, 2018

Abstract

A method for a polymeric or nanocomposite material. The method includes assembling a multiphase hard-soft structure, where the structure includes a hard micro- or nano-phase, and a soft micro- or nano-phase that includes a polymeric scaffold. In the method, the polymeric scaffold includes dynamically interacting motifs and has a glass transition temperature (T g ) lower than the intended operating temperature of the material.

First claim

What is claimed is:

1. A method of obtaining a polymeric or composite material, comprising
assembling a multiphase hard-soft structure that comprises
a hard microphase, and
a soft micro- or nano-phase comprising a polymeric scaffold,

wherein the polymeric scaffold comprises dynamically interacting motifs and has a glass transition temperature (T g ) lower than the intended operating temperature of the material,
wherein the hard phase comprises an amorphous or crystalline assembly of oligomers or polymers having a melting temperature (Tm) or a Tg higher than the intended operating temperature of the material,
wherein the dynamically interacting motifs are supramolecular interaction motifs comprising mono-dentate or multi-dentate hydrogen bonding groups, ionic interacting groups, pi-pi stacking groups, metal-ligand interacting groups, or hydrophobic interacting groups,
wherein the soft phase is covalently linked to the hard phase,
wherein the Tm and Tg for the hard phase oligomers or polymers is in the range of −50° C. to 350° C., the intended operating temperature of use is in the range of −100° C. to 300° C., and the Tg for the soft phase polymers is in the range of −150° C. to 250° C., and
wherein the hard phase is prepared from a polymer which assembles into a spherical or cylindrical microstructure upon processing, and the soft phase comprises homo-oligomers or homo-polymers comprising dynamically interacting motifs, co-oligomers or co-polymers comprising different dynamically interacting motifs, or co-oligomers or co-polymers comprising dynamically interacting motifs and an additional functional co-monomer.

2. The method of claim 1 , wherein the soft phase comprises a linear, branched, hyper-branched or dendritic polymeric structure, or a combination thereof.

3. The method of claim 2 , wherein the soft phase comprises acrylic, polyvinyl, polysiloxane, polyester or polyethylene.

4. The method of claim 1 , wherein the hard phase comprises styrene, polynorbornene or polycarbonate.

5. The method of claim 1 , wherein the assembling comprises:
obtaining an oligomer or polymer for formation of the hard phase, the oligomer or polymer comprising functional groups for attachment to the polymeric scaffold;
preparing oligomeric or polymeric macromolecules attached to the oligomer or polymer by growth of the macromolecules from the oligomer or polymer, or by attachment of pre-synthesized macromolecules to the oligomer or polymer, wherein the macromolecules comprise monomers bearing the dynamically interacting motifs; and
processing the oligomeric or polymeric macromolecules attached to the oligomer or polymer to produce the multiphase hard-soft structure.

6. The method of claim 1 , wherein the soft phase comprises oligomers or polymers comprising dynamically interacting motifs as well as latent covalent cross-linking functional groups which form permanent covalent connections in the soft phase.

7. The method of claim 1 , wherein the soft phase comprises oligomers or polymers comprising dynamically interacting motifs as well as a filler or other soft-phase reinforcement material.

8. The method of claim 1 , wherein the soft phase comprises co-oligomers or co-polymers comprising dynamically interacting motifs and one or more non-DIM functional monomers.

9. The method of claim 1 , wherein the Tm and the Tg of the hard phase is higher than the Tg of the soft phase.

10. The method of claim 1 , wherein the spherical or cylindrical microstructure is a structure with one or more domain dimensions in the range of 1-1000 nm.

11. The method of claim 1 , wherein the hard phase comprises preformed micro- or nano-objects selected from the group consisting of spheres, cubes, fibrils, rods and sheets, and a combination thereof.

12. A nanocomposite material which is self-healing at an intended operating temperature and which is a multiphase hard-soft structure that comprises:
a hard micro- or nano-phase, and
a soft micro- or nano-phase comprising a polymeric scaffold having dynamically interacting motifs,
wherein the soft phase has a glass transition temperature (Tg) lower than the intended operation temperature of the material,
wherein the hard phase comprises (i) an amorphous or crystalline assembly of oligomers or polymers having a melting temperature (Tm) higher than the intended operating temperature of the material, or (ii) an amorphous or crystalline assembly of oligomers or polymers having a Tg higher than the intended operating temperature of the material, or (iii) a preformed micro- or nano-object selected from the group consisting of spheres, cubes, fibrils, rods, and sheets, or (iv) a combination thereof,
wherein the soft phase is covalently linked to the hard phase,
wherein the Tm and Tg for the hard phase oligomers or polymers is in the range of −50° C. to 350° C., the intended operating temperature of use is in the range of −100° C. to 300° C., and the Tg for the soft phase polymers is in the range of −150° C. to 250° C., and
wherein the dynamic interacting motifs are supramolecular interaction motifs comprising a metal-ligand interacting group, and the metal-ligand interacting group comprises an imidazole moiety and a metal cation.

13. A composite material which is self-healing at an intended operating temperature and which is a multiphase hard-soft structure that comprises:
a hard micro- or nano-phase, and
a soft micro- or nano-phase comprising a polymeric scaffold having dynamically interacting motifs,
wherein the soft phase has a glass transition temperature (Tg) lower than the intended operation temperature of the material,
wherein the dynamically interacting motifs are supramolecular interaction motifs comprising at least one of mono-dentate or multi-dentate hydrogen bonding groups, ionic interaction groups, pi-pi stacking groups, metal-ligand interacting groups, or hydrophobic interacting groups,
wherein the hard phase comprises (i) an amorphous or crystalline assembly of oligomers or polymers having a melting temperature (Tm) higher than the intended operating temperature of the material, or (ii) an amorphous or crystalline assembly of oligomers or polymers having a Tg higher than the intended operating temperature of the material, or (iii) a preformed micro- or nano-object selected from the group consisting of spheres, cubes, fibrils, rods, and sheets, or (iv) a combination thereof,
wherein the soft phase is covalently linked to the hard phase,
wherein the Tm and Tg for the hard phase oligomers or polymers is in the range of −50° C. to 350° C., the intended operating temperature of use is in the range of −100° C. to 300° C., and the Tg for the soft phase polymers is in the range of −150° C. to 250° C., and
wherein the hard phase is prepared from a polymer which assembles into a spherical or cylindrical microstructure upon processing when the hard phase comprises (i) or (ii), and
wherein the soft phase comprises homo-oligomers or homo-polymers comprising dynamically interacting motifs, co-oligomers or co-polymers comprising different dynamically interacting motifs, or co-oligomers or co-polymers comprising dynamically interacting motifs and an additional functional co-monomer.

14. A nanocomposite material which is self-healing at an intended operating temperature and which is a multiphase hard-soft structure that comprises:
a hard micro- or nano-phase, and
a soft micro- or nano-phase comprising a polymeric scaffold having dynamically interacting motifs,
wherein the soft phase has a glass transition temperature (Tg) lower than the intended operation temperature of the material,
wherein the hard phase compris

Assignees

• Univ California

Inventors

• Kushner Aaron M
• Guan Zhibin
• Williams Gregory
• Chen Yulin

Classifications

• C08L51/10

  grafted on to inorganic materials · CPC title

• C08G83/008

  Supramolecular polymers · CPC title

• C08K3/36 Primary

  Silica · CPC title

• C08F292/00

  Macromolecular compounds obtained by polymerising monomers on to inorganic materials · CPC title

• C08F293/005

  using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent · CPC title