Golf ball consisting of an inner part comprising at least an elastomeric polymer and a reinforcing agent comprising graphene nano-platelets in which at least 90% of the nano-platelets has a lateral size (x, y) from 50 to 50,000 nm and a thickness (z) from 0.34 to 45 nm, and a C/O ratio ≥100:1.

The present invention relates to a partially oxidized graphene and a method for preparing the same. Since the partially oxidized graphene is prepared by subjecting the partially oxidized graphite to a high pressure homogenization, the exfoliation efficiency is excellent, the inherent characteristics of graphene are maintained even without using a reduction step after exfoliation, and the dispersibility thereof in organic solvents is excellent, and thus the invention can be applied to various fields.

A graphene nanostructure has a nanographene, a π conjugated functional group bonded to the nanographene via a pyrazine skeleton, and at least one Br group and/or at least one CN group introduced into the π conjugated functional group. A graphene nanostructure preferably has an average size of 1 nm or larger to 100 nm or smaller, a band gap of 0.01 eV or higher to 1.2 eV or lower, and/or a HOMO level of −6.0 eV or higher to −4.0 eV or lower. As the π conjugated functional group into which the Br group(s) and/or the CN group(s) are/is introduced, a 4-bromobenzene group, a 4,5-dibromobenzene group, a 5-bromopyridine group, a 5-bromopyrazine group, a benzonitrile group, a phthalonitrile group, or a 2,3-dicyanopyrazine group is desirable.

The present disclosure provides a method of graphene exfoliation and/or stabilization. Both graphene and silica are mixed in an organic solvent to form a liquid precursor, which is then directed through an orifice formed by a metal cylinder and a flat metal plate. The metal cylinder is pressed against the flat metal plate by a high pressure. The high shear between the metal cylinder and the flat metal plate breaks down the thick layers of graphene to thin layers, which are stably dispersed in the gel formed by the silica.

A method for preparing a three-dimensional porous graphene material, including: a) constructing a CAD model corresponding to a required three-dimensional porous structure, and designing an external shape and internal structure parameters of the model; b) based on the CAD model, preparing a three-dimensional porous metal structure using a metal powder as material; c) heating the three-dimensional porous metal structure and preparing a metal template of the required three-dimensional porous structure; d) placing the metal template in a tube furnace and heating the metal template to a temperature of between 800 and 1000° C.; standing for 0.5-1 hr, introducing a carbon source to the tube furnace for continued reaction, cooling resulting products to room temperature to yield a three-dimensional graphene grown on the metal template; and e) preparing a corrosive solution, and immersing the three-dimensional graphene in the corrosive solution.

In order to prepare highly conductive and highly dispersible graphene and obtain an electrode for a lithium ion battery with good output characteristics and cycle characteristics, there is provided a graphene composition containing thiourea, the element ratio of sulfur to carbon being 0.04 or more and 0.12 or less in X-ray photoelectron spectroscopy measurement.

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 %.

A lithium ion secondary battery includes at least a positive electrode, a negative electrode, and an electrolyte solution. The negative electrode includes a negative electrode current collector and a negative electrode mixture layer. The negative electrode mixture layer is formed on a surface of the negative electrode current collector. The negative electrode mixture layer includes graphite particles, inorganic filler particles, lithium titanate particles, and a water-based binder. The inorganic filler particles have an average primary particle size that is ½ or less of an average primary particle size of the graphite particles. The lithium titanate particles have an average primary particle size of 1 μm or less. A ratio of an average primary particle size of the lithium titanate particles with respect to an average primary particle size of the inorganic filler particles is one or less.

A graphene oxide Janus nanosheets relatively permeability modifier (RPM) for carbonate formations. The graphene oxide Janus nanosheets RPM may be used to treat a water and hydrocarbon producing carbonate formation to reduce water permeability in the formation and increase the production of hydrocarbons. The graphene oxide Janus nanosheet RPM includes a first side having negatively charged functional groups and a second side having alkyl groups. The alkyl groups may include C8 to C30 alkyls. The negatively charged functional groups may include carboxyl groups, epoxy groups, and hydroxyl groups. Methods of reducing water permeability of a carbonate formation using the graphene oxide Janus nanosheets RPM and methods of manufacturing the graphene oxide Janus nanosheets RPM are also provided.