IP Library Granted Patent US 8,501,319
Granted Patent B2
US 8,501,319 · App. 12/676,129 · Granted Aug 6, 2013

Pre-formed assemblies of solgel-derived nanoparticles as 3D scaffolds for composites and aerogels

Inventors: Nicholas Leventis (Rolla, MO); Chariklia Sotiriou-Leventis (Rolla, MO)
Assignee: The Curators of the University of Missouri, University of Missouri System, Office of Technology and Special Projects
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Quick Facts
Patent No.
US 8,501,319
App. No.
12/676,129
Granted
Aug 6, 2013
Kind
B2
Abstract

A composite material that includes a dopant comprised of pre-formed, three dimensional assemblies of skeletal structures that are comprised of solgel derived nanoparticles. The composite material includes a chemically bonded, in situ formed, polymer coating that at least partially coats mesoporous surfaces of the nanoparticles to provide enhancement of random dispersion of the dopant and to minimize or avoid agglomeration. Further, the polymer may be functionalized or the mesoporous surfaces of the nanoparticles may be treated to enable stronger chemical bonding between the dopant and the polymer.

Claims (36)

1. A composite material, comprising:

pre-formed, three dimensional assemblies of skeletal structures comprising nanoparticles having mesoporous surfaces, said skeletal structures comprising mesoporous spaces; and

a polymerized-in-place polymer coating at least partially coating the mesoporous surfaces of the nanoparticles;

wherein the polymer coating at least substantially fills the mesoporous spaces of said skeletal structures.

2. The composite material of claim 1 , wherein the polymer coating comprises a conformal coating.

3. The composite material of claim 1 , wherein the three dimensional assemblies are formed by chemical modification of skeletal structures in a co-gelation process of tetramethoxysilane and a bidentate free radical initiator.

4. The composite material of claim 3 , wherein the three dimensional assemblies are formed by chemical modification of skeletal structures in a co-gelation process of tetramethoxysilane and a bidentate free radical initiator, wherein the bidentate free radical initiator is of the formula:

5. The composite material of claim 4 , wherein the assemblies of skeletal structures are predispersed within a polymer matrix.

6. The composite material of claim 3 , wherein the three dimensional assemblies are formed by chemical modification of skeletal structures in a co-gelation process of tetramethoxysilane and a bidentate free radical initiator, wherein the bidentate free radical initiator is of the formula:

7. The composite material of claim 1 , further comprising a chemical coupling agent forming a bridge between the polymer coating and mesoporous surfaces of the nanoparticles.

8. The composite material of claim 7 , wherein the coupling agent comprises a silane.

9. The composite material of claim 1 , wherein the flexural strength of a monolith of the composite material comprising skeletal structures having the polymer coating is about 300 times greater than a second composite material having a skeletal structure of nanoparticles lacking the polymer coating and the density of the composite material is less than about 4 times that of the second composite material.

10. A composite material comprising:

pre-formed, three dimensional assemblies of skeletal structures comprising nanoparticles having mesoporous surfaces, said skeletal structures comprising mesoporous spaces, the assemblies substantially uniformly dispersed within the composite material; and

a polymerized-in-place polymer coating at least partially coating the mesoporous surfaces of the nanoparticles, and at least substantially filling the mesoporous spaces of said skeletal structures.

11. The composite material of claim 10 , wherein the skeletal structures comprises an aerogel.

12. The composite material of claim 10 , wherein the polymer coating comprises a conformal polymer coating.

13. The composite material of claim 10 , further comprising a chemical coupling agent forming a bridge between the polymer coating and mesoporous surfaces of the nanoparticles.

14. The composite material of claim 13 , wherein the coupling agent comprises a silane.

15. The composite material of claim 10 , wherein the skeletal structures comprise silica.

16. The composite material of claim 15 wherein the skeletal structures are formed in a sol gel process.

17. The composite material of claim 16 , wherein the polymer is selected from polyimide, polymethylmethacrylate, polystyrene and other polyolefins, epoxy, polyurethane, polyurea.

18. The composite material of claim 10 , wherein the flexural strength of the aerogel having the polymer coating is about 300 times greater than a second aerogel lacking the polymerized-in-place polymer coating, and the density of the aerogel less than about 4 times that of the second aerogel.

19. The composite material of claim 10 , wherein the polymer is selected from polyimide, polymethylmethacrylate, polystyrene and other polylefins, epoxy, polyurethane, and polyurea.

20. A composite material comprising:

pre-formed, three dimensional assemblies of skeletal structures comprising nanoparticles having mesoporous surfaces, said skeletal structures comprising mesoporous spaces, the nanoparticles derived from solgel, the assemblies substantially uniformly dispersed with the composite material; and

a polymerized-in-place polymer coating at least partially coating and adhered to mesoporous surfaces of the nanoparticles, the polymer coating adherence to the mesoporous surfaces being enhanced by chemical bonding;

wherein the polymer coating at least substantially fills the mesoporous spaces of said skeletal structures.

21. The composite material of claim 20 , further comprising a chemical coupling agent forming a bridge between the polymer coating and mesoporous surfaces of the nanoparticles.

22. The composite material of claim 20 , wherein the flexural strength of the aerogel having the polymerized-in-place polymer coating is about 300 times greater than a second aerogel lacking the polymerized-in-place polymer coating and the density of the aerogel is less than 3 times that of the second aerogel.

23. The composite material of claim 20 , wherein the polymer coating comprises a conformal polymer coating.

24. A composite material having a silica dopant comprised of a 3D assembly of skeletal structures comprised of sol-gel derived nanoparticles having mesoporous surfaces, said skeletal structures comprising mesoporous spaces, wherein the silica has been surface-modified to form a chemical bond with an in situ-formed polymer matrix, the polymer matrix forming a chemical continuum with the dopant, wherein the polymer matrix forms a polymer coating, and wherein the polymer coating at least substantially fills the mesoporous spaces of said skeletal structures.

25. A method of manufacturing a composite material having a silica dopant comprised of a 3D assembly of skeletal structures comprised of sol-gel derived nanoparticles having mesoporous surfaces, the skeletal structures having mesoporous spaces, the method comprising:

forming wet gels substantially comprised of strands of nanoparticles distributed in said 3D skeletal structures comprising mesoporous spaces, the nanoparticles derived from a silica dopant by means of a sol-gel process,

exchanging pore-filling solvent with monomer precursors able to develop chemical bonding with the surface of silica, and

polymerizing the monomer to form a polymer coating which at least substantially fills the space between the strands of nanoparticles and the mesoporous spaces of said skeletal structures.

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 18, 2015
From: MISSOURI UNIVERSITY OF SCIENCE AND TECHNOLOGY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 037127/0907 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2010
From: LEVENTIS, NICHOLAS; SOTIRIOU-LEVENTIS, CHARIKLIA
To: THE CURATORS OF THE UNIVERSITY OF MISSOURI
Reel/Frame 024097/0109 →
Continuity (3)
Provisional Application 60970741 · Sep 7, 2007
Provisional Application 60970742 · Sep 7, 2007
Related Publication 20100310831A1 · Dec 9, 2010