In situ exfoliation method to fabricate a graphene-reinforced polymer matrix composite (G-PMC)
US-9896565-B2 · Feb 20, 2018 · US
US12460064B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12460064-B2 |
| Application number | US-202117374522-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 13, 2021 |
| Priority date | Oct 19, 2012 |
| Publication date | Nov 4, 2025 |
| Grant date | Nov 4, 2025 |
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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.
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What is claimed is: 1 . A graphene-reinforced polymer matrix composite, comprising a distribution of graphite microparticles and mechanically exfoliated single-or multi-layer graphene nanoparticles in a thermoplastic polymer matrix, wherein the composite comprises contamination-free graphene-polymer interfaces, wherein the polymer adheres to or is covalently bonded to the graphene-polymer interfaces, wherein the single-or multi-layer graphene nanoparticles are directionally aligned, thereby providing one-, two- or three-dimensional reinforcement of the polymer matrix phase, and wherein between about 50% to about 90% by weight of the graphite microparticles and the single-or multi-layer graphene nanoparticles are the single-or multi-layer graphene nanoparticles. 2 . The graphene-reinforced polymer matrix composite of claim 1 , wherein the directional alignment of the single-or multi-layer graphene nanoparticles is achieved by an in situ exfoliation of graphite in a molten thermoplastic polymer phase. 3 . The graphene-reinforced polymer matrix composite of claim 2 , wherein the in situ exfoliation of graphite is performed by using a single screw extruder with axial fluted extensional mixing elements or spiral fluted extensional mixing elements. 4 . The graphene-reinforced polymer matrix composite of claim 1 , wherein the single- or multi-layer graphene nanoparticles comprise essentially pure and uncontaminated single- or multi-layer graphene nanoparticles. 5 . The graphene-reinforced polymer matrix composite of claim 4 , wherein the single- or multi-layer graphene nanoparticles comprise essentially pure and uncontaminated graphene nanoparticles less than 25 nanometers thick along a c-axis direction. 6 . The graphene-reinforced polymer matrix composite of claim 4 , wherein the single- or multi layer graphene nanoparticles comprise essentially pure and uncontaminated graphene nanoparticles less than IO nanometers thick along a c-axis direction. 7 . The graphene-reinforced polymer matrix composite of claim 1 , 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 graphene-reinforced polymer matrix composite of claim 1 , wherein the composite comprises between about0.1% and about 50% by weight of graphene. 9 . The graphene-reinforced polymer matrix composite of claim 1 , wherein the composite comprises between about 5% and about 50% by weight of graphene. 10 . The graphene-reinforced polymer matrix composite of claim 1 , wherein the composite comprises between about 10% and about 30% by weight of graphene. 11 . The graphene-reinforced polymer matrix composite of claim 1 , wherein the composite comprises between about 0.1% and about 30% by weight of essentially pure and uncontaminated graphene nanoparticles. 12 . The graphene-reinforced polymer matrix composite of claim 2 , wherein the graphite comprises expanded graphite. 13 . The graphene-reinforced polymer matrix composite of claim 2 , wherein the graphite doped with other elements to modify a surface chemistry of the single- or multi-layer graphene nanoparticles. 14 . The graphene-reinforced polymer matrix composite of claim 2 , 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. 15 . A polymer composition comprising a host thermoplastic polymer and the graphene-reinforced polymer matrix composite of claim 1 distributed therein. 16 . The polymer composition of claim 15 , wherein the host thermoplastic 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. 17 . The graphene-reinforced polymer matrix composite of claim 1 , wherein the composite is fabricated by an in situ exfoliation process, comprising: distributing graphite microparticles into a molten thermoplastic polymer phase, wherein at least 50% by weight of the graphite in the graphite microparticles consists of multi-layer graphite crystals between 1.0 and 1000 microns thick along a c-axis direction; and applying a succession of shear strain events to the molten polymer phase in situ 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 mechanically exfoliates the graphite successively with each event until said graphite is at least partially exfoliated to form a distribution in the molten polymer phase of essentially pure and uncontaminated single- and multi-layer graphene nanoparticles less than 25 nanometers thick along the c-axis direction.
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