A method for the manufacture of reduced graphene oxide from kish graphite including: A. The provision of kish graphite, B. Optionally, a pre-treatment of kish graphite, C. The intercalation of kish graphite with a persulfate salt and an acid at room temperature to obtain intercalated kish graphite, D. The expansion of the intercalated kish graphite to obtain expanded kish graphite and E. An oxidation step of the expanded kish graphite to obtain graphene oxide and F. A reduction of graphene oxide into reduced graphene oxide.

A graphene product obtained from Graphene Nanofibers (GNFs), having a modified crystal structure and a defined size distribution. The product is non toxic and has useful biological properties such as modification of the adipocytes phenotype. The product can be used in cosmetics.

The invention provides a method for preparing graphene which method comprises the steps of: (a) forming a graphite/water mixture; and (b) introducing the graphite/water mixture into a cavitation reactor using at least two offset nozzles; a cavitation reactor for use in the method wherein the cavitation reactor has a cavitation chamber wherein the cavitation chamber has at least two offset inlet nozzles which are directed towards the centre of the cavitation chamber and at least one outlet; and graphene having a carbon content of at least about 98 wt %.

Provided herein are graphene nanoribbons with high structural uniformity and low levels of impurities and methods of synthesis thereof. Also provided herein are graphene nanoplatelets of superior structural uniformity and low levels of impurities and methods of synthesis thereof. Further provided herein are mixtures of graphene nanoribbons and graphene nanoplatelets of good structural uniformity and low levels of impurities and methods of synthesis thereof. The method includes, for example, the steps of depositing catalyst on a constantly moving substrate, forming carbon nanotubes on the substrate, separating carbon nanotubes from the substrate, collecting the carbon nanotubes from the surface where the substrate moves continuously and sequentially through the depositing, forming, separating and collecting steps. Further processing steps convert the synthesized carbon nanotubes to graphene nanoribbons, graphene nanoplatelets and mixtures thereof.

The present invention relates to an antiviral composition comprising graphene quantum dots as an active ingredient, and has been completed by identifying that the graphene quantum dots can exert an antiviral effect by inhibiting the ability of a virus to infect cells. Therefore, the antiviral composition according to the present invention is expected to not only be utilized in various forms, such as a film, a fiber, clothing, food, feed, and a disinfectant, for preventing or blocking viral infections, but also be used as an effective therapeutic factor for viral diseases.

Methods include producing tunable carbon structures and combining carbon structures with a polymer to form a composite material. Carbon structures include crinkled graphene. Methods also include functionalizing the carbon structures, either in-situ, within the plasma reactor, or in a liquid collection facility. The plasma reactor has a first control for tuning the specific surface area (SSA) of the resulting tuned carbon structures as well as a second, independent control for tuning the SSA of the tuned carbon structures. The composite materials that result from mixing the tuned carbon structures with a polymer results in composite materials that exhibit exceptional favorable mechanical and/or other properties. Mechanisms that operate between the carbon structures and the polymer yield composite materials that exhibit these exceptional mechanical properties are also examined.

A method for continuously mass-manufacturing graphene using thermal plasma, the method for continuously mass-manufacturing graphene includes the steps of: (a) injecting an inert gas into a plasma device to generate plasma; (b) injecting expandable graphite and graphite intercalation compounds (GIC) into the plasma device in constant amounts; and (c) allowing the expandable graphite and GIC to be expanded by thermal plasma treatment so that graphene is exfoliated.

A method of producing high conductivity carbon material from coal includes subjecting the coal to a dissolution process to produce a solubilized coal material, and subjecting the solubilized coal material to a pyrolysis process to produce the high conductivity carbon material.

A voltage tunable solar-blind UV detector using a EG/SiC heterojunction based Schottky emitter bipolar phototransistor with EG grown on p-SiC epi-layer using a chemically accelerated selective etching process of Si using TFS precursor.

Methods include producing tunable carbon structures and combining carbon structures with a polymer to form a composite material. Carbon structures include crinkled graphene. Methods also include functionalizing the carbon structures, either in-situ, within the plasma reactor, or in a liquid collection facility. The plasma reactor has a first control for tuning the specific surface area (SSA) of the resulting tuned carbon structures as well as a second, independent control for tuning the SSA of the tuned carbon structures. The composite materials that result from mixing the tuned carbon structures with a polymer results in composite materials that exhibit exceptional favorable mechanical and/or other properties. Mechanisms that operate between the carbon structures and the polymer yield composite materials that exhibit these exceptional mechanical properties are also examined.