In situ exfoliation method to fabricate a graphene-reinforced polymer matrix composite (G-PMC)

US9896565B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9896565-B2
Application numberUS-201314437040-A
CountryUS
Kind codeB2
Filing dateMar 14, 2013
Priority dateOct 19, 2012
Publication dateFeb 20, 2018
Grant dateFeb 20, 2018

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

A method for forming a graphene-reinforced polymer matrix composite is disclosed. The method includes distributing graphite microparticles into a molten thermoplastic polymer phase; and applying a succession of shear strain events to the molten polymer phase so that the molten polymer phase exfoliates the graphite successively with each event until at least 50% of the graphite is exfoliated to form a distribution in the molten polymer phase of single- and multi-layer graphene nanoparticles less than 50 nanometers thick along the c-axis direction.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for forming a graphene-reinforced polymer matrix composite, comprising: (a) distributing graphite microparticles into a molten thermoplastic polymer phase, wherein at least 50% by weight of the graphite in the graphite microparticles consists of multilayer graphite crystals between 1.0 and 1000 microns thick along a c-axis direction; and (b) applying a succession of shear strain events to the molten polymer phase so that the shear stress within said molten polymer phase is equal to or greater than the Interlayer Shear Strength (ISS) of said graphite microparticles and said molten polymer phase exfoliates the graphite successively with each event said graphite is at least partially exfoliated to form a distribution in the molten polymer phase of single- and multi-layer graphene nanoparticles less than 10 nanometers thick along the c-axis direction; (c) wherein the amount of graphite added to said polymer phase in combination with the number of shear strain events are effective to provide graphene-reinforced polymer matrix composites or polymer master batches containing between about 1.0 and about 50 wt % pure and uncontaminated graphene. 2. The method of claim 1 , wherein the graphite particles are prepared by crushing and grinding a graphite-containing mineral to millimeter-sized dimensions. 3. The method of claim 2 , wherein the millimeter-sized particles are reduced to micron-sized dimensions using ball milling and attritor milling. 4. The method of claim 3 , wherein the graphite particles are extracted from the micron-sized particle mixture by a flotation method. 5. The method of claim 4 , wherein the extracted graphite particles are incorporated in a polymer matrix using a single screw extruder with axial fluted extensional mixing elements or spiral fluted extensional mixing elements. 6. The method of claim 5 , wherein the graphite-containing polymer matrix is subjected to repeated extrusion to induce exfoliation of the graphitic material, thus forming a uniform dispersion of graphene nanoparticles in the polymer matrix. 7. The method of claim 6 , wherein the polymer is selected from the group consisting of polyether-etherketones, polyetherketones, polyphenylene sulfides, poly-ethylene sulfides, polyetherimides, polyvinylidene fluorides, polysulfones, polycarbonates, poly-phenylene ethers/oxides, nylons, aromatic thermoplastic polyesters, aromatic polysulfones, thermoplastic polyimides, liquid crystal polymers, thermoplastic elastomers, polyethylenes, polypropylenes, polystyrene, polymethylmethacrylate, polyacrylonitrile, ultra-high-molecular-weight polyethylene, polytetrafluoroethylene, acrylonitrile butadiene styrene, polyamides, poly-phenylene oxide, polyoxymethylene plastic, polyimides, polyaryletherketones, polyvinylchloride, acrylics, and mixtures of two or more thereof. 8. The method of claim 1 , wherein the succession of shear strain events is applied until at least 50% by weight of the graphite is exfoliated to form a distribution in the molten polymer phase of single- and multi-layer graphene nanoparticles less than 10 nanometers thick along the c-axis direction. 9. The method of claim 1 , wherein the succession of shear strain events is applied until at least 90% by weight of the graphite is exfoliated to form a distribution in the molten polymer phase of single- and multi-layer graphene nanoparticles less than 10 nanometers thick along the c-axis direction. 10. The method of claim 1 , wherein the succession of shear strain events is applied until at least 80% by weight of the graphite is exfoliated to form a distribution in the molten polymer phase of single- and multi-layer graphene nanoparticles less than 10 nanometers thick along the c-axis direction. 11. The method of claim 1 , wherein the succession of shear strain events is applied until at least 75% by weight of the graphite is exfoliated to form a distribution in the molten polymer phase of single- and multi-layer graphene nanoparticles less than 10 nanometers thick along the c-axis direction. 12. The method of claim 1 , wherein the succession of shear strain events is applied until at least 70% by weight of the graphite is exfoliated to form a distribution in the molten polymer phase of single- and multi-layer graphene nanoparticles less than 10 nanometers thick along the c-axis direction. 13. The method of claim 1 , wherein the succession of shear strain events is applied until at least 60% by weight of the graphite is exfoliated to form a distribution in the molten polymer phase of single- and multi-layer graphene nanoparticles less than 10 nanometers thick along the c-axis direction. 14. The method of claim 1 , wherein the graphite is doped with other elements to modify a surface chemistry of the exfoliated graphene nanoparticles. 15. The method of claim 1 , wherein the graphite is expanded graphite. 16. The method of claim 1 , wherein a surface chemistry or nanostructure of the dispersed graphite is modified to enhance bond strength with the polymer matrix to increase strength and stiffness of the graphene composite. 17. The method of claim 1 , wherein the graphene nanoparticles are directionally aligned thereby providing one-, two- or three-dimensional reinforcement of the polymer matrix phase. 18. The method of claim 1 , wherein said graphene-reinforced polymer matrix composite contains residual graphite microparticles. 19. A graphene-reinforced polymer matrix composite prepared by the method of claim 1 . 20. The graphene-reinforced polymer matrix composite of claim 19 , wherein said composite contains between about 0.1% and about 30% by weight of graphene. 21. The graphene-reinforced polymer matrix composite of claim 19 , wherein said composite contains between about 1% and about 10% by weight of graphene. 22. The graphene-reinforced polymer matrix composite of claim 19 , wherein said composite contains between about 5% and about 50% by weight of graphene. 23. The graphene-reinforced polymer matrix composite of claim 19 , wherein said composite contains between about 10% and about 30% by weight of graphene. 24. The graphene-reinforced polymer matrix composite of claim 19 , wherein the polymer is selected from the group consisting of polyether-etherketones, polyetherketones, poly-phenylene sulfides, polyethylene sulfides, polyetherimides, polyvinylidene fluorides, polysulfones, polycarbonates, polyphenylene ethers/oxides, nylons, aromatic thermoplastic polyesters, aromatic polysulfones, thermoplastic polyimides, liquid crystal polymers, thermoplastic elastomers, poly-ethylenes, polypropylenes, polystyrene, polymethylmethacrylate, polyacrylonitrile, ultra-high-molecular- weight polyethylene, polytetrafluoroethylene, acrylonitrile butadiene styrene, poly-amides, polyphenylene oxide, polyoxymethylene plastic, polyimides, polyaryletherketones, polyvinylchloride, acrylics, and mixtures thereof. 25. The graphene-reinforced polymer matrix composite of claim 19 comprising residual graphite microparticles. 26. A graphene-reinforced polymer matrix composite comprising a thermoplastic polymer bonded or adhered to single- and/or multi-layer graphene nanoparticles, wherein said nanoparticles are less than 10 nanometers thick along a c-axis direction, and wherein said composite contains between about 0.1% and about 30% by weight of pure and uncontaminated graphene. 27. The graphene-reinforced po

Assignees

Inventors

Classifications

  • Polysulfones; Polyethersulfones · CPC title

  • Nanostructured additives · CPC title

  • Reinforced macromolecular compounds with nanosized materials, e.g. nanoparticles, nanofibres, nanotubes, nanowires, nanorods or nanolayered materials · CPC title

  • Thermoplastic resins · CPC title

  • C08K3/04Primary

    Carbon · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9896565B2 cover?
A method for forming a graphene-reinforced polymer matrix composite is disclosed. The method includes distributing graphite microparticles into a molten thermoplastic polymer phase; and applying a succession of shear strain events to the molten polymer phase so that the molten polymer phase exfoliates the graphite successively with each event until at least 50% of the graphite is exfoliated to …
Who is the assignee on this patent?
Univ Rutgers
What technology area does this patent fall under?
Primary CPC classification C08K3/04. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 20 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).