A method for the manufacture of pristine graphite from Kish graphite including three different steps A, B and C; the pristine obtained with among others a high amount of carbon atoms, i.e. a pristine graphene having a high purity; and the use of this pristine graphene.

A method for the manufacture of pristine graphite from Kish graphite including three different steps A, B and C; the pristine obtained with among others a high amount of carbon atoms, i.e. a pristine graphene having a high purity; and the use of this pristine graphene.

The invention provides a method for the production of graphene-structured products. The method generally comprises contacting at a conversion temperature ranging from about 850° C. to about 1100° C. in an inert atmosphere coal with a molten salt to produce a graphene-structured product. In an alternate embodiment, the method comprises contacting at a conversion temperature ranging from about 850° C. to about 1100° C. in an inert atmosphere coal with a molten salt to produce a graphene-structured product; and, separating a rare earth element from the graphene-structured product.

The invention provides a method for the production of graphene-structured products. The method generally comprises contacting at a conversion temperature ranging from about 850° C. to about 1100° C. in an inert atmosphere coal with a molten salt to produce a graphene-structured product. In an alternate embodiment, the method comprises contacting at a conversion temperature ranging from about 850° C. to about 1100° C. in an inert atmosphere coal with a molten salt to produce a graphene-structured product; and, separating a rare earth element from the graphene-structured product.

A porous graphene film, its manufacturing method and an electronic product are provided. The method of manufacturing the porous graphene film includes: mixing a dispersion liquid of graphene with a dispersion liquid of particles, and performing a film-forming process to form a mixed film of graphene and particles; and removing the particles in the mixed film of graphene and particles to form the porous graphene film. The porous graphene film prepared by the method has a large specific surface area and an excellent electroconductivity.

A porous graphene film, its manufacturing method and an electronic product are provided. The method of manufacturing the porous graphene film includes: mixing a dispersion liquid of graphene with a dispersion liquid of particles, and performing a film-forming process to form a mixed film of graphene and particles; and removing the particles in the mixed film of graphene and particles to form the porous graphene film. The porous graphene film prepared by the method has a large specific surface area and an excellent electroconductivity.

The method for synthesizing graphene derivatives from asphaltene includes one or more steps that are based on thermal and/or chemical treatments. In the thermal treatment, asphaltene was carbonized in a rotating quartz-tube furnace under an inert atmosphere (N.sub.2). This carbonization process was performed at a temperature range of 400-950° C. The carbonization process converted asphaltene molecules into graphene derivatives by eliminating the alkyl side chains, exfoliating the aromatic layers (n), and expanding the aromatic sheet diameter (L.sub.a). The chemical treatment, on the other hand, was performed on the asphaltene (i.e., graphene precursor) by dispersing the asphaltene molecules in a liquid intercalating agent to functionalize the asphaltene and expand the inter-layer distance between the aromatic sheets (intercalation). In this intercalation process, the graphitic surface of asphaltene is oxidized to form asphaltene oxide, and then graphene oxide (GO), which is a nonconductive hydrophilic carbon material.

The method for synthesizing graphene derivatives from asphaltene includes one or more steps that are based on thermal and/or chemical treatments. In the thermal treatment, asphaltene was carbonized in a rotating quartz-tube furnace under an inert atmosphere (N.sub.2). This carbonization process was performed at a temperature range of 400-950° C. The carbonization process converted asphaltene molecules into graphene derivatives by eliminating the alkyl side chains, exfoliating the aromatic layers (n), and expanding the aromatic sheet diameter (L.sub.a). The chemical treatment, on the other hand, was performed on the asphaltene (i.e., graphene precursor) by dispersing the asphaltene molecules in a liquid intercalating agent to functionalize the asphaltene and expand the inter-layer distance between the aromatic sheets (intercalation). In this intercalation process, the graphitic surface of asphaltene is oxidized to form asphaltene oxide, and then graphene oxide (GO), which is a nonconductive hydrophilic carbon material.

Provided are graphene nanosheets having a polyaromatic hydrocarbon concentration of less than about 0.7% by weight and a tap density of less than about 0.08 g/cm.sup.3, as measured by ASTM B527-15 standard. The graphene nanosheets also have a specific surface area (B.E.T) greater than about 250 m.sup.2/g. Also provided are processes for producing graphene nanosheets as well as for removing polyaromatic hydrocarbons from graphene nanosheets, comprising heating said graphene nanosheets under oxidative atmosphere, at a temperature of at least about 200° C.

Provided are graphene nanosheets having a polyaromatic hydrocarbon concentration of less than about 0.7% by weight and a tap density of less than about 0.08 g/cm.sup.3, as measured by ASTM B527-15 standard. The graphene nanosheets also have a specific surface area (B.E.T) greater than about 250 m.sup.2/g. Also provided are processes for producing graphene nanosheets as well as for removing polyaromatic hydrocarbons from graphene nanosheets, comprising heating said graphene nanosheets under oxidative atmosphere, at a temperature of at least about 200° C.