The process of claim 1, wherein step (c) includes forming a graphene oxide layer mass having an inter-plane spacing d 00 2 of 0.4 nm to 0.7 nm and an oxygen content no less than 20% by weight; and step (d) includes heat-treating the graphene oxide layer mass to an extent that an inter-plane spacing d 00 2 is decreased to a value of from 0.3354 nm to 0.36 nm and the oxygen content is decreased to less than 2% by weight.

The process of claim 1, wherein said graphene oxide gel has a viscosity greater than 2,000 centipoise when measured at 20 ° C prior to said shear-induced thinning and the viscosity is reduced to less than 2,000 centipoise during or after shear-induced thinning.

The process of claim 1, wherein said graphene oxide gel has a viscosity from 500 centipoise to 500,000 centipoise when measured at 20 * C prior to said shear-induced thinning 2

The process of claim 1, wherein said graphene oxide gel has a viscosity no less than 5,000 centipoise when measured at 20 * C prior to said shear-induced thinning and the viscosity is reduced to less than 2,000 centipoise during or after shear-induced thinning.

The process of claim 1, wherein said graphene oxide gel has a viscosity that decreases by at least 10 times when a shear rate is increased at 20 *C.

The process of claim 1, wherein shear-induced thinning is conducted via a procedure selected from coating, casting, injection molding, compression molding, resin- transfer molding, extrusion, pultrusion, filament winding.

The process of claim 1, wherein said step (d) includes heat treating said graphene oxide layer mass under a compressive stress.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 100 nm.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 100 nm but less than 10 pm.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 10 pm.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 100 pm.

The process of claim 1, wherein said graphene oxide gel is prepared by immersing a graphitic material in a powder or fibrous form in an oxidizing liquid to form an initially optically opaque and dark suspension in a reaction vessel at a reaction temperature for a length of time sufficient to obtain a graphene oxide gel that is a homogeneous solution and also optically transparent, translucent, or brown-colored, wherein said graphene oxide gel is composed of graphene oxide molecules dissolved in an acidic medium having a p H value of no higher than 5 and said graphene oxide molecules have an oxygen content no less than 20% by weight.

The process of claim 1, wherein said graphene oxide gel is prepared by immersing a graphitic material in an oxidizing agent to form an initially optically opaque and dark suspension and allowing an oxidizing reaction to proceed until a homogeneous and 3 optically transparent, translucent, or brown-color solution is formed, and wherein said graphitic material is selected from natural graphite, artificial graphite, meso-phase carbon, meso-phase pitch, meso-carbon micro-bead, soft carbon, hard carbon, coke, carbon fiber, carbon nano-fiber, carbon nano-tube, or a combination thereof.

The process of claim 1, wherein said steps (b) and (c) include feeding a sheet of a solid substrate material from a roller to a deposition zone, depositing a layer of graphene oxide gel onto a surface of said sheet of solid substrate material to form a graphene oxide gel layer thereon, drying said graphene oxide gel to form a dried graphene oxide layer deposited on said substrate surface, and collecting graphene oxide layer-deposited substrate sheet on a collector roller.

The process of claim 1, wherein the unitary graphene material further contains a discrete solid carbon, graphite, or graphene filler phase dispersed in said unitary graphene material to form a unitary graphene matrix composite structure and said filler phase is selected from a carbon or graphite fiber, carbon or graphite nano-fiber, carbon nano-tube, carbon nano-rod, meso-phase carbon particle, meso-carbon micro-bead, expanded graphite flake with a thickness greater than 100 nm, single-layer graphene sheet, multi-layer graphene platelet with a thickness less than 100 nm, exfoliated graphite or graphite worm, coke particle, needle coke, carbon black or acetylene black particle, activated carbon particle, or a combination thereof; wherein said carbon, graphite, or graphene filler phase occupies a weight fraction of 0.01% to 99% based on the total composite structure weight.

The process of claim 1, wherein said heat treatment temperature contains a temperature in a thermal reduction regime of 100 ° C-500 * C and the unitary graphene material has an oxygen content less than 5%, an inter-graphene spacing less than 0.4 nm, and/or a thermal conductivity of at least 100 W/mK.

The process of claim 1, wherein said heat treatment temperature contains a temperature in the range of 500 * C-1,250 * C and the unitary graphene material has an oxygen content less than 1%, an inter-graphene spacing less than 0.345 nm, a thermal conductivity of at least 1,300 W/mK, and/or an electrical conductivity no less than 3,000 S/cm.

The process of claim 1, wherein said heat treatment temperature contains a temperature in the range of 1,250 * C- 2,000 * C and the unitary graphene material has an 4 oxygen content less than 0.01%, an inter-graphene spacing less than 0.337 nm, a thermal conductivity of at least 1,500 W/mK, and/or an electrical conductivity no less than 5,000 S/cm.

The process of claim 1, wherein said heat treatment temperature contains a temperature greater than 2,000 * C and the unitary graphene material has an oxygen content no greater than 0.001%, an inter-graphene spacing less than 0.336 n m, a mosaic spread value no greater than 0.7, a thermal conductivity of at least 1,700 W/mK, and/or an electrical conductivity no less than 10,000 S/cm.

The process of claim 1, wherein said heat treatment temperature contains a temperature no less than 2,500 * C and the unitary graphene material has an inter-graphene spacing less than 0.336 nm, a mosaic spread value no greater than 0.4, a thermal conductivity greater than 1,700 W/mK, and/or an electrical conductivity greater than 10,000 S/cm.

The process of claim 1, wherein the unitary graphene material exhibits an inter- graphene spacing less than 0.337 nm and a mosaic spread value less than 1.0.

The process of claim 1, wherein the unitary graphene material exhibits a degree of graphitization no less than 40% and/or a mosaic spread value less than 0.7.

The process of claim 1, wherein the unitary graphene material exhibits a degree of graphitization no less than 80% and/or a mosaic spread value no greater than 0.4.

The process of claim 1, wherein said unitary graphene material contains chemically bonded graphene molecules or chemically merged graphene planes that are parallel to one another.

The process of claim 1, wherein said unitary graphene material contains no complete grain boundary therein, is a graphene single crystal, or a poly-crystal graphene structure with graphene molecules being oriented along a preferred direction.

The process of claim 1, wherein said graphene oxide gel is obtained from a graphitic material having a maximum original graphite grain size and said unitary graphene material is a single crystal or a poly-crystal graphene structure having a grain size larger than said maximum original grain size.

The process of claim 1, wherein said graphene oxide gel is obtained from a graphitic material having multiple graphite crystallites exhibiting no preferred crystalline orientation as determined by an X-ray diffraction or electron diffraction method and wherein said unitary graphene material is a single crystal or a poly-crystal graphene structure having a preferred crystalline orientation as determined by said X-ray diffraction or electron diffraction method.

The process of claim 1, wherein said unitary graphene material contains a combination of sp2 and sp 3 electronic configurations.

The process of claim 1, wherein said graphene oxide gel is obtained by immersing a graphitic material in a powder or fibrous form in an oxidizing liquid medium in a reaction vessel at a reaction temperature for a length of time sufficient to obtain a homogeneous solution composed of graphene oxide molecules dissolved in the liquid medium, wherein said homogeneous solution is optically transparent, translucent, or brown colored and said graphene oxide molecules have an oxygen content no less than 20% by weight and a molecular weight less than 43,000 g/mole while in a gel state.

The process of claim 1, wherein said step of heat-treating induces chemical linking, merging, or chemical bonding of graphene oxide molecules, and/or re-graphitization or re-organization of a graphitic structure.

The process of claim 1, wherein said unitary graphene material has an electrical conductivity greater than 3,000 S/cm, a thermal conductivity greater than 600 W/m K, a physical density greater than 1.8 g/cm3, and/or a tensile strength greater than 40 MPa.

The process of claim 1, wherein said unitary graphene material has an electrical conductivity greater than 5,000 S/cm, a thermal conductivity greater than 1,000 W/mK, a physical density greater than 1.9 g/cm3, and/or a tensile strength greater than 60 MPa.

The process of claim 1, wherein step (c) includes forming a graphene oxide layer mass having an inter-plane spacing d 00 2 of 0.4 nm to 0.7 nm and an oxygen content no less than 20% by weight; and step (d) includes heat-treating the graphene oxide layer mass to an extent that an inter-plane spacing d 00 2 is decreased to a value of from 0.3354 nm to 0.36 nm and the oxygen content is decreased to less than 2% by weight.

The process of claim 1, wherein said graphene oxide gel has a viscosity greater than 2,000 centipoise when measured at 20 ° C prior to said shear-induced thinning and the viscosity is reduced to less than 2,000 centipoise during or after shear-induced thinning.

The process of claim 1, wherein said graphene oxide gel has a viscosity from 500 centipoise to 500,000 centipoise when measured at 20 * C prior to said shear-induced thinning 2

The process of claim 1, wherein said graphene oxide gel has a viscosity no less than 5,000 centipoise when measured at 20 * C prior to said shear-induced thinning and the viscosity is reduced to less than 2,000 centipoise during or after shear-induced thinning.

The process of claim 1, wherein said graphene oxide gel has a viscosity that decreases by at least 10 times when a shear rate is increased at 20 *C.

The process of claim 1, wherein shear-induced thinning is conducted via a procedure selected from coating, casting, injection molding, compression molding, resin- transfer molding, extrusion, pultrusion, filament winding.

The process of claim 1, wherein said step (d) includes heat treating said graphene oxide layer mass under a compressive stress.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 100 nm.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 100 nm but less than 10 pm.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 10 pm.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 100 pm.

The process of claim 1, wherein said graphene oxide gel is prepared by immersing a graphitic material in a powder or fibrous form in an oxidizing liquid to form an initially optically opaque and dark suspension in a reaction vessel at a reaction temperature for a length of time sufficient to obtain a graphene oxide gel that is a homogeneous solution and also optically transparent, translucent, or brown-colored, wherein said graphene oxide gel is composed of graphene oxide molecules dissolved in an acidic medium having a p H value of no higher than 5 and said graphene oxide molecules have an oxygen content no less than 20% by weight.

The process of claim 1, wherein said graphene oxide gel is prepared by immersing a graphitic material in an oxidizing agent to form an initially optically opaque and dark suspension and allowing an oxidizing reaction to proceed until a homogeneous and 3 optically transparent, translucent, or brown-color solution is formed, and wherein said graphitic material is selected from natural graphite, artificial graphite, meso-phase carbon, meso-phase pitch, meso-carbon micro-bead, soft carbon, hard carbon, coke, carbon fiber, carbon nano-fiber, carbon nano-tube, or a combination thereof.

The process of claim 1, wherein said steps (b) and (c) include feeding a sheet of a solid substrate material from a roller to a deposition zone, depositing a layer of graphene oxide gel onto a surface of said sheet of solid substrate material to form a graphene oxide gel layer thereon, drying said graphene oxide gel to form a dried graphene oxide layer deposited on said substrate surface, and collecting graphene oxide layer-deposited substrate sheet on a collector roller.

The process of claim 1, wherein the unitary graphene material further contains a discrete solid carbon, graphite, or graphene filler phase dispersed in said unitary graphene material to form a unitary graphene matrix composite structure and said filler phase is selected from a carbon or graphite fiber, carbon or graphite nano-fiber, carbon nano-tube, carbon nano-rod, meso-phase carbon particle, meso-carbon micro-bead, expanded graphite flake with a thickness greater than 100 nm, single-layer graphene sheet, multi-layer graphene platelet with a thickness less than 100 nm, exfoliated graphite or graphite worm, coke particle, needle coke, carbon black or acetylene black particle, activated carbon particle, or a combination thereof; wherein said carbon, graphite, or graphene filler phase occupies a weight fraction of 0.01% to 99% based on the total composite structure weight.

The process of claim 1, wherein said heat treatment temperature contains a temperature in a thermal reduction regime of 100 ° C-500 * C and the unitary graphene material has an oxygen content less than 5%, an inter-graphene spacing less than 0.4 nm, and/or a thermal conductivity of at least 100 W/mK.

The process of claim 1, wherein said heat treatment temperature contains a temperature in the range of 500 * C-1,250 * C and the unitary graphene material has an oxygen content less than 1%, an inter-graphene spacing less than 0.345 nm, a thermal conductivity of at least 1,300 W/mK, and/or an electrical conductivity no less than 3,000 S/cm.

The process of claim 1, wherein said heat treatment temperature contains a temperature in the range of 1,250 * C- 2,000 * C and the unitary graphene material has an 4 oxygen content less than 0.01%, an inter-graphene spacing less than 0.337 nm, a thermal conductivity of at least 1,500 W/mK, and/or an electrical conductivity no less than 5,000 S/cm.

The process of claim 1, wherein said heat treatment temperature contains a temperature greater than 2,000 * C and the unitary graphene material has an oxygen content no greater than 0.001%, an inter-graphene spacing less than 0.336 n m, a mosaic spread value no greater than 0.7, a thermal conductivity of at least 1,700 W/mK, and/or an electrical conductivity no less than 10,000 S/cm.

The process of claim 1, wherein said heat treatment temperature contains a temperature no less than 2,500 * C and the unitary graphene material has an inter-graphene spacing less than 0.336 nm, a mosaic spread value no greater than 0.4, a thermal conductivity greater than 1,700 W/mK, and/or an electrical conductivity greater than 10,000 S/cm.

The process of claim 1, wherein the unitary graphene material exhibits an inter- graphene spacing less than 0.337 nm and a mosaic spread value less than 1.0.

The process of claim 1, wherein the unitary graphene material exhibits a degree of graphitization no less than 40% and/or a mosaic spread value less than 0.7.

The process of claim 1, wherein the unitary graphene material exhibits a degree of graphitization no less than 80% and/or a mosaic spread value no greater than 0.4.

The process of claim 1, wherein said unitary graphene material contains chemically bonded graphene molecules or chemically merged graphene planes that are parallel to one another.

The process of claim 1, wherein said unitary graphene material contains no complete grain boundary therein, is a graphene single crystal, or a poly-crystal graphene structure with graphene molecules being oriented along a preferred direction.

The process of claim 1, wherein said graphene oxide gel is obtained from a graphitic material having a maximum original graphite grain size and said unitary graphene material is a single crystal or a poly-crystal graphene structure having a grain size larger than said maximum original grain size.

The process of claim 1, wherein said graphene oxide gel is obtained from a graphitic material having multiple graphite crystallites exhibiting no preferred crystalline orientation as determined by an X-ray diffraction or electron diffraction method and wherein said unitary graphene material is a single crystal or a poly-crystal graphene structure having a preferred crystalline orientation as determined by said X-ray diffraction or electron diffraction method.

The process of claim 1, wherein said unitary graphene material contains a combination of sp2 and sp 3 electronic configurations.

The process of claim 1, wherein said graphene oxide gel is obtained by immersing a graphitic material in a powder or fibrous form in an oxidizing liquid medium in a reaction vessel at a reaction temperature for a length of time sufficient to obtain a homogeneous solution composed of graphene oxide molecules dissolved in the liquid medium, wherein said homogeneous solution is optically transparent, translucent, or brown colored and said graphene oxide molecules have an oxygen content no less than 20% by weight and a molecular weight less than 43,000 g/mole while in a gel state.

The process of claim 1, wherein said step of heat-treating induces chemical linking, merging, or chemical bonding of graphene oxide molecules, and/or re-graphitization or re-organization of a graphitic structure.

The process of claim 1, wherein said unitary graphene material has an electrical conductivity greater than 3,000 S/cm, a thermal conductivity greater than 600 W/m K, a physical density greater than 1.8 g/cm3, and/or a tensile strength greater than 40 MPa.

The process of claim 1, wherein said unitary graphene material has an electrical conductivity greater than 5,000 S/cm, a thermal conductivity greater than 1,000 W/mK, a physical density greater than 1.9 g/cm3, and/or a tensile strength greater than 60 MPa.

The process of claim 1, wherein step (c) includes forming a graphene oxide layer mass having an inter-plane spacing d 00 2 of 0.4 nm to 0.7 nm and an oxygen content no less than 20% by weight; and step (d) includes heat-treating the graphene oxide layer mass to an extent that an inter-plane spacing d 00 2 is decreased to a value of from 0.3354 nm to 0.36 nm and the oxygen content is decreased to less than 2% by weight.

The process of claim 1, wherein said graphene oxide gel has a viscosity greater than 2,000 centipoise when measured at 20 ° C prior to said shear-induced thinning and the viscosity is reduced to less than 2,000 centipoise during or after shear-induced thinning.

The process of claim 1, wherein said graphene oxide gel has a viscosity from 500 centipoise to 500,000 centipoise when measured at 20 * C prior to said shear-induced thinning 2

The process of claim 1, wherein said graphene oxide gel has a viscosity no less than 5,000 centipoise when measured at 20 * C prior to said shear-induced thinning and the viscosity is reduced to less than 2,000 centipoise during or after shear-induced thinning.

The process of claim 1, wherein said graphene oxide gel has a viscosity that decreases by at least 10 times when a shear rate is increased at 20 *C.

The process of claim 1, wherein shear-induced thinning is conducted via a procedure selected from coating, casting, injection molding, compression molding, resin- transfer molding, extrusion, pultrusion, filament winding.

The process of claim 1, wherein said step (d) includes heat treating said graphene oxide layer mass under a compressive stress.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 100 nm.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 100 nm but less than 10 pm.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 10 pm.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 100 pm.

The process of claim 1, wherein said graphene oxide gel is prepared by immersing a graphitic material in a powder or fibrous form in an oxidizing liquid to form an initially optically opaque and dark suspension in a reaction vessel at a reaction temperature for a length of time sufficient to obtain a graphene oxide gel that is a homogeneous solution and also optically transparent, translucent, or brown-colored, wherein said graphene oxide gel is composed of graphene oxide molecules dissolved in an acidic medium having a p H value of no higher than 5 and said graphene oxide molecules have an oxygen content no less than 20% by weight.

The process of claim 1, wherein said graphene oxide gel is prepared by immersing a graphitic material in an oxidizing agent to form an initially optically opaque and dark suspension and allowing an oxidizing reaction to proceed until a homogeneous and 3 optically transparent, translucent, or brown-color solution is formed, and wherein said graphitic material is selected from natural graphite, artificial graphite, meso-phase carbon, meso-phase pitch, meso-carbon micro-bead, soft carbon, hard carbon, coke, carbon fiber, carbon nano-fiber, carbon nano-tube, or a combination thereof.

The process of claim 1, wherein said steps (b) and (c) include feeding a sheet of a solid substrate material from a roller to a deposition zone, depositing a layer of graphene oxide gel onto a surface of said sheet of solid substrate material to form a graphene oxide gel layer thereon, drying said graphene oxide gel to form a dried graphene oxide layer deposited on said substrate surface, and collecting graphene oxide layer-deposited substrate sheet on a collector roller.

The process of claim 1, wherein the unitary graphene material further contains a discrete solid carbon, graphite, or graphene filler phase dispersed in said unitary graphene material to form a unitary graphene matrix composite structure and said filler phase is selected from a carbon or graphite fiber, carbon or graphite nano-fiber, carbon nano-tube, carbon nano-rod, meso-phase carbon particle, meso-carbon micro-bead, expanded graphite flake with a thickness greater than 100 nm, single-layer graphene sheet, multi-layer graphene platelet with a thickness less than 100 nm, exfoliated graphite or graphite worm, coke particle, needle coke, carbon black or acetylene black particle, activated carbon particle, or a combination thereof; wherein said carbon, graphite, or graphene filler phase occupies a weight fraction of 0.01% to 99% based on the total composite structure weight.

The process of claim 1, wherein said heat treatment temperature contains a temperature in a thermal reduction regime of 100 ° C-500 * C and the unitary graphene material has an oxygen content less than 5%, an inter-graphene spacing less than 0.4 nm, and/or a thermal conductivity of at least 100 W/mK.

The process of claim 1, wherein said heat treatment temperature contains a temperature in the range of 500 * C-1,250 * C and the unitary graphene material has an oxygen content less than 1%, an inter-graphene spacing less than 0.345 nm, a thermal conductivity of at least 1,300 W/mK, and/or an electrical conductivity no less than 3,000 S/cm.

The process of claim 1, wherein said heat treatment temperature contains a temperature in the range of 1,250 * C- 2,000 * C and the unitary graphene material has an 4 oxygen content less than 0.01%, an inter-graphene spacing less than 0.337 nm, a thermal conductivity of at least 1,500 W/mK, and/or an electrical conductivity no less than 5,000 S/cm.

The process of claim 1, wherein said heat treatment temperature contains a temperature greater than 2,000 * C and the unitary graphene material has an oxygen content no greater than 0.001%, an inter-graphene spacing less than 0.336 n m, a mosaic spread value no greater than 0.7, a thermal conductivity of at least 1,700 W/mK, and/or an electrical conductivity no less than 10,000 S/cm.

The process of claim 1, wherein said heat treatment temperature contains a temperature no less than 2,500 * C and the unitary graphene material has an inter-graphene spacing less than 0.336 nm, a mosaic spread value no greater than 0.4, a thermal conductivity greater than 1,700 W/mK, and/or an electrical conductivity greater than 10,000 S/cm.

The process of claim 1, wherein the unitary graphene material exhibits an inter- graphene spacing less than 0.337 nm and a mosaic spread value less than 1.0.

The process of claim 1, wherein the unitary graphene material exhibits a degree of graphitization no less than 40% and/or a mosaic spread value less than 0.7.

The process of claim 1, wherein the unitary graphene material exhibits a degree of graphitization no less than 80% and/or a mosaic spread value no greater than 0.4.

The process of claim 1, wherein said unitary graphene material contains chemically bonded graphene molecules or chemically merged graphene planes that are parallel to one another.

The process of claim 1, wherein said unitary graphene material contains no complete grain boundary therein, is a graphene single crystal, or a poly-crystal graphene structure with graphene molecules being oriented along a preferred direction.

The process of claim 1, wherein said graphene oxide gel is obtained from a graphitic material having a maximum original graphite grain size and said unitary graphene material is a single crystal or a poly-crystal graphene structure having a grain size larger than said maximum original grain size.

The process of claim 1, wherein said graphene oxide gel is obtained from a graphitic material having multiple graphite crystallites exhibiting no preferred crystalline orientation as determined by an X-ray diffraction or electron diffraction method and wherein said unitary graphene material is a single crystal or a poly-crystal graphene structure having a preferred crystalline orientation as determined by said X-ray diffraction or electron diffraction method.

The process of claim 1, wherein said unitary graphene material contains a combination of sp2 and sp 3 electronic configurations.

The process of claim 1, wherein said graphene oxide gel is obtained by immersing a graphitic material in a powder or fibrous form in an oxidizing liquid medium in a reaction vessel at a reaction temperature for a length of time sufficient to obtain a homogeneous solution composed of graphene oxide molecules dissolved in the liquid medium, wherein said homogeneous solution is optically transparent, translucent, or brown colored and said graphene oxide molecules have an oxygen content no less than 20% by weight and a molecular weight less than 43,000 g/mole while in a gel state.

The process of claim 1, wherein said step of heat-treating induces chemical linking, merging, or chemical bonding of graphene oxide molecules, and/or re-graphitization or re-organization of a graphitic structure.

The process of claim 1, wherein said unitary graphene material has an electrical conductivity greater than 3,000 S/cm, a thermal conductivity greater than 600 W/m K, a physical density greater than 1.8 g/cm3, and/or a tensile strength greater than 40 MPa.

The process of claim 1, wherein said unitary graphene material has an electrical conductivity greater than 5,000 S/cm, a thermal conductivity greater than 1,000 W/mK, a physical density greater than 1.9 g/cm3, and/or a tensile strength greater than 60 MPa.

The process of claim 1, wherein step (c) includes forming a graphene oxide layer mass having an inter-plane spacing d 00 2 of 0.4 nm to 0.7 nm and an oxygen content no less than 20% by weight; and step (d) includes heat-treating the graphene oxide layer mass to an extent that an inter-plane spacing d 00 2 is decreased to a value of from 0.3354 nm to 0.36 nm and the oxygen content is decreased to less than 2% by weight.

The process of claim 1, wherein said graphene oxide gel has a viscosity greater than 2,000 centipoise when measured at 20 ° C prior to said shear-induced thinning and the viscosity is reduced to less than 2,000 centipoise during or after shear-induced thinning.

The process of claim 1, wherein said graphene oxide gel has a viscosity from 500 centipoise to 500,000 centipoise when measured at 20 * C prior to said shear-induced thinning 2

The process of claim 1, wherein said graphene oxide gel has a viscosity no less than 5,000 centipoise when measured at 20 * C prior to said shear-induced thinning and the viscosity is reduced to less than 2,000 centipoise during or after shear-induced thinning.

The process of claim 1, wherein said graphene oxide gel has a viscosity that decreases by at least 10 times when a shear rate is increased at 20 *C.

The process of claim 1, wherein shear-induced thinning is conducted via a procedure selected from coating, casting, injection molding, compression molding, resin- transfer molding, extrusion, pultrusion, filament winding.

The process of claim 1, wherein said step (d) includes heat treating said graphene oxide layer mass under a compressive stress.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 100 nm.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 100 nm but less than 10 pm.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 10 pm.

The process of claim 1, wherein said unitary graphene material has a thickness greater than 100 pm.

The process of claim 1, wherein said graphene oxide gel is prepared by immersing a graphitic material in a powder or fibrous form in an oxidizing liquid to form an initially optically opaque and dark suspension in a reaction vessel at a reaction temperature for a length of time sufficient to obtain a graphene oxide gel that is a homogeneous solution and also optically transparent, translucent, or brown-colored, wherein said graphene oxide gel is composed of graphene oxide molecules dissolved in an acidic medium having a p H value of no higher than 5 and said graphene oxide molecules have an oxygen content no less than 20% by weight.

The process of claim 1, wherein said graphene oxide gel is prepared by immersing a graphitic material in an oxidizing agent to form an initially optically opaque and dark suspension and allowing an oxidizing reaction to proceed until a homogeneous and 3 optically transparent, translucent, or brown-color solution is formed, and wherein said graphitic material is selected from natural graphite, artificial graphite, meso-phase carbon, meso-phase pitch, meso-carbon micro-bead, soft carbon, hard carbon, coke, carbon fiber, carbon nano-fiber, carbon nano-tube, or a combination thereof.

The process of claim 1, wherein said steps (b) and (c) include feeding a sheet of a solid substrate material from a roller to a deposition zone, depositing a layer of graphene oxide gel onto a surface of said sheet of solid substrate material to form a graphene oxide gel layer thereon, drying said graphene oxide gel to form a dried graphene oxide layer deposited on said substrate surface, and collecting graphene oxide layer-deposited substrate sheet on a collector roller.

The process of claim 1, wherein the unitary graphene material further contains a discrete solid carbon, graphite, or graphene filler phase dispersed in said unitary graphene material to form a unitary graphene matrix composite structure and said filler phase is selected from a carbon or graphite fiber, carbon or graphite nano-fiber, carbon nano-tube, carbon nano-rod, meso-phase carbon particle, meso-carbon micro-bead, expanded graphite flake with a thickness greater than 100 nm, single-layer graphene sheet, multi-layer graphene platelet with a thickness less than 100 nm, exfoliated graphite or graphite worm, coke particle, needle coke, carbon black or acetylene black particle, activated carbon particle, or a combination thereof; wherein said carbon, graphite, or graphene filler phase occupies a weight fraction of 0.01% to 99% based on the total composite structure weight.

The process of claim 1, wherein said heat treatment temperature contains a temperature in a thermal reduction regime of 100 ° C-500 * C and the unitary graphene material has an oxygen content less than 5%, an inter-graphene spacing less than 0.4 nm, and/or a thermal conductivity of at least 100 W/mK.

The process of claim 1, wherein said heat treatment temperature contains a temperature in the range of 500 * C-1,250 * C and the unitary graphene material has an oxygen content less than 1%, an inter-graphene spacing less than 0.345 nm, a thermal conductivity of at least 1,300 W/mK, and/or an electrical conductivity no less than 3,000 S/cm.

The process of claim 1, wherein said heat treatment temperature contains a temperature in the range of 1,250 * C- 2,000 * C and the unitary graphene material has an 4 oxygen content less than 0.01%, an inter-graphene spacing less than 0.337 nm, a thermal conductivity of at least 1,500 W/mK, and/or an electrical conductivity no less than 5,000 S/cm.

The process of claim 1, wherein said heat treatment temperature contains a temperature greater than 2,000 * C and the unitary graphene material has an oxygen content no greater than 0.001%, an inter-graphene spacing less than 0.336 n m, a mosaic spread value no greater than 0.7, a thermal conductivity of at least 1,700 W/mK, and/or an electrical conductivity no less than 10,000 S/cm.

The process of claim 1, wherein said heat treatment temperature contains a temperature no less than 2,500 * C and the unitary graphene material has an inter-graphene spacing less than 0.336 nm, a mosaic spread value no greater than 0.4, a thermal conductivity greater than 1,700 W/mK, and/or an electrical conductivity greater than 10,000 S/cm.

The process of claim 1, wherein the unitary graphene material exhibits an inter- graphene spacing less than 0.337 nm and a mosaic spread value less than 1.0.

The process of claim 1, wherein the unitary graphene material exhibits a degree of graphitization no less than 40% and/or a mosaic spread value less than 0.7.

The process of claim 1, wherein the unitary graphene material exhibits a degree of graphitization no less than 80% and/or a mosaic spread value no greater than 0.4.

The process of claim 1, wherein said unitary graphene material contains chemically bonded graphene molecules or chemically merged graphene planes that are parallel to one another.

The process of claim 1, wherein said unitary graphene material contains no complete grain boundary therein, is a graphene single crystal, or a poly-crystal graphene structure with graphene molecules being oriented along a preferred direction.

The process of claim 1, wherein said graphene oxide gel is obtained from a graphitic material having a maximum original graphite grain size and said unitary graphene material is a single crystal or a poly-crystal graphene structure having a grain size larger than said maximum original grain size.

The process of claim 1, wherein said graphene oxide gel is obtained from a graphitic material having multiple graphite crystallites exhibiting no preferred crystalline orientation as determined by an X-ray diffraction or electron diffraction method and wherein said unitary graphene material is a single crystal or a poly-crystal graphene structure having a preferred crystalline orientation as determined by said X-ray diffraction or electron diffraction method.

The process of claim 1, wherein said unitary graphene material contains a combination of sp2 and sp 3 electronic configurations.

The process of claim 1, wherein said graphene oxide gel is obtained by immersing a graphitic material in a powder or fibrous form in an oxidizing liquid medium in a reaction vessel at a reaction temperature for a length of time sufficient to obtain a homogeneous solution composed of graphene oxide molecules dissolved in the liquid medium, wherein said homogeneous solution is optically transparent, translucent, or brown colored and said graphene oxide molecules have an oxygen content no less than 20% by weight and a molecular weight less than 43,000 g/mole while in a gel state.

The process of claim 1, wherein said step of heat-treating induces chemical linking, merging, or chemical bonding of graphene oxide molecules, and/or re-graphitization or re-organization of a graphitic structure.

The process of claim 1, wherein said unitary graphene material has an electrical conductivity greater than 3,000 S/cm, a thermal conductivity greater than 600 W/m K, a physical density greater than 1.8 g/cm3, and/or a tensile strength greater than 40 MPa.

The process of claim 1, wherein said unitary graphene material has an electrical conductivity greater than 5,000 S/cm, a thermal conductivity greater than 1,000 W/mK, a physical density greater than 1.9 g/cm3, and/or a tensile strength greater than 60 MPa.