Graft polymerization initiated on graphitic nanomaterials and their nanocomposite formation

Patent metadata

Field	Value
Publication number	US-9688538-B2
Application number	US-201514614982-A
Country	US
Kind code	B2
Filing date	Feb 5, 2015
Priority date	Feb 5, 2014
Publication date	Jun 27, 2017
Grant date	Jun 27, 2017

Abstract

An improved graft polymerization method from general graphitic structures with organic based monomers through the mechanism of Reversible Addition-Fragmentation Chain Transfer (RAFT) polymerization was developed. Organic hybrid nanomaterials comprising graphitic structures are covalently bonded via chemically reactive groups on the outer walls of the structure. Methods for forming the covalently bonded structures to many organic based monomers and/or polymers may occur through RAFT polymerization utilizing dithioester as a chain transfer agent. The method may also comprise nanocomposite formation of such organic hybrid nanomaterials with common plastic(s) to form graphitic nanocomposite reinforced plastic articles.

First claim

What is claimed is:

1. A method for forming a graphitic nanocomposite comprising:
functionalizing at least one graphitic nanomaterial, wherein the at least one graphitic nanomaterial is functionalized by thiolating a surface; and
mixing the at least one graphitic nanomaterial with at least one free-radical initiator and at least one type of monomer in at least one type of organic solution to provide a reaction mixture, wherein the reaction mixture forms a polymerized graphitic nanocomposite, the at least one graphitic nanomaterial is linked to another graphitic nanomaterial by a linking structure, and the at least one free-radical initiator is azobisisobutyronitrile (AIBN), 4,4′-azobis(4-cyanovaleric acid), 1,1′-azobis(cyclohexanecarbonitrile), or 2,2′-azobis(2-methylpropionamidine) dihydrochloride,
wherein further the linking structure comprises a dithioester and the at least one type of monomer, and a ratio of the at least one graphitic nanomaterial to a polymer provided by the graphitic nanocomposite is equal to or between about 10 to 30%.

2. The method of claim 1 , wherein the polymerized graphitic nanocomposite exhibits conductivity equal to or greater than 1 S/m.

3. The method of claim 1 , wherein the polymerized graphitic nanocomposite has a processing temperature equal to or greater than 1° C.

4. The method of claim 1 , wherein the polymerized graphitic nanocomposite exhibits improved physical strength equal to or greater than 1% in comparison to a polymer of the at least one monomer.

5. The method of claim 1 , wherein a ratio of the at least one graphitic nanomaterial to a polymer provided by the graphitic nanocomposite is equal to or between about 20 to 30%.

6. The method of claim 2 , wherein the polymerized graphitic nanocomposite has a color or transparency different from a polymer of the at least one type of monomer without the graphitic nanomaterials.

7. The method of claim 1 , wherein the mixing step provides for Reversible Addition-Fragmentation Chain Transfer (RAFT) polymerization.

8. The method of claim 1 , wherein the at least one graphitic nanomaterial is carbon black, carbon fiber, graphite, graphene, graphene oxides, carbon nanotubes, or fullerenes.

9. The method of claim 1 , wherein the functionalizing step is performed with phosphorus pentasulfide (P 4 S 10 ), Lawesson's reagent: 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide (C 14 H 14 O 2 P 2 S 4 ), Belleau's Reagent: 2,4-Bis(4-phenoxyphenyl)-1,3-dithia-2,4-diphosphetane-2,4-disulfide (C 24 H 18 O 2 P 2 S 4 ) or Davy's Reagent: 2,4-Bis(methylthio)-1,3,2,4-dithiadiphosphetane-2,4-disulfide (C 2 H 6 P 2 S 6 ).

10. The method of claim 1 , wherein the at least one graphitic nanomaterial is carboxylized prior to the functionalizing step.

11. The method of claim 1 , wherein the at least one type of monomer is a methacrylate, methacrylamide, acrylonitrile, styrene, butadiene, vinyl acetate, or octadecyl acrylate.

12. The method of claim 1 , wherein the at least one organic solution is toluene, N-methyl-2-pyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, 4-butyrolactone or 1,3-dimethyl-2-imidazolidinone.

13. The method of claim 1 , wherein the polymerized graphitic nanocomposite comprises a polymer selected from polyethylene (PE), poly(methyl methacrylate) (PMMA), acrylonitrile-butadiene-styrene copolymers (ABS), polycarbonate (PC), or polyurethane (PU).

14. The method of claim 1 , wherein the reaction mixture is refluxed for equal to or between 12 to 48 hours.

15. The method of claim 1 , wherein the reaction mixture is refluxed at temperatures equal to or between 110 to 200° C.

16. The method of claim 14 , further comprising:
cooling the reaction mixture;
adding tetrahydrofuran to the reaction mixture;
adding the reaction mixture to methanol; and
precipitating a polymerized graphitic nanocomposite.

17. The method of claim 1 , further comprising:
removing solvents from the reaction mixture; and
curing the reaction mixture at a temperature equal to or between 25-400° C.

18. The method of claim 17 , wherein the reaction mixture is cured for 1 second to 24 hours.

Assignees

• Curran Seamus
• Liao Kang-Shyang
• Wang Alexander
• Univ Houston System

Inventors

• Curran Seamus
• Liao Kang-Shyang
• Wang Alexander

Classifications

• C01B32/174

  Derivatisation; Solubilisation; Dispersion in solvents · CPC title

• C08J2323/06

  Polyethene · CPC title

• C08J2355/02

  Acrylonitrile-Butadiene-Styrene [ABS] polymers · CPC title

• C01B32/194

  After-treatment · CPC title

• C08J2333/12

  Homopolymers or copolymers of methyl methacrylate · CPC title