The present application pertains to dispersions comprising oxidized, discrete carbon nanotubes and high-surface area carbon nanotubes. The oxidized, discrete carbon nanotubes comprise an interior and exterior surface, each surface comprising an interior surface oxidized species content and an exterior surface oxidized species content. The interior surface oxidized species content differs from the exterior surface oxidized species content by at least 20%, and as high as 100%. The high-surface area nanotubes are generally single-wall nanotubes. The BET surface area of the high-surface area nanotubes is from about 550 m.sup.2/g to about 1500 m.sup.2/g according to ASTM D6556-16. The aspect ratio is at least about 500 up to about 6000. The dispersions comprise from about 0.1 to about 30% by weight nanotubes based on the total weight of the dispersion.

A method for preparing porous inorganic particles is disclosed. The method includes the steps of: (a) preparing an emulsion comprising an inorganic precursor and a polar solvent; (b) adding an organic solvent to the emulsion of step (a) to swell emulsion particles; (c) mixing the swollen emulsion of step (b) with polymer particles having a positive charge on the surface thereof; (d) adding a surfactant to the mixture of step (c) and removing the organic solvent; (e) adding an initiator to the result of step (d) to polymerize the same; and (f) firing the result of step (e) to remove the polymer particles so as to form macropores.

A method of forming a titania-coated inorganic particle comprising the steps of (a) stirring a mixture of a titania precursor such as a titanium alkoxide and an inorganic particle such as a hollow glass particles in an organic solvent such as an alcohol for more than 1 h to cause adsorption of the titania precursor on the surface of the inorganic particle; and (b) adding water dropwise to the mixture under stirring to convert the titania precursor to titania which then forms a coating on the inorganic particle. A method for forming a paint formulation, a titania-coated inorganic particle, a paint formulation comprising a titania-coated inorganic particle and use of a titania-coated inorganic particle in a paint formulation is also described.

Preparation of two-dimensional indium selenide, other two-dimensional materials and related compositions via surfactant-free deoxygenated co-solvent systems.

The present disclosure relates to a composition that includes a metal chalcogenide having a surface and a ligand, where the ligand is covalently bound to the surface. In some embodiments of the present disclosure, the metal chalcogenide may be defined by MX.sub.z, where Z is between 1 and 3, inclusively, M (a metal) includes at least one of Sc, Zr, Hf, Zr, Ti, Nb, Ta, V, Mo, Cr, Re, W, S, Pt, Fe, Cu, Sb, In, Zn, Cd, P, and/or Mn, and X (a chalcogenide) includes at least one of S, Se, and/or Te.

The powder of the magnetoplumbite-type hexagonal ferrite is an aggregate of particles of a compound represented by Formula (1), and, in a particle size distribution based on number measured by a laser diffraction scattering method, in a case where a mode value is defined as a mode diameter, a diameter at a cumulative percentage of 10% is defined as D10 and a diameter at a cumulative percentage of 90% is defined as D90, the mode diameter is equal to or greater than 5 μm and less than 10 μm and an expression of (D90−D10)/mode diameter≤3.0 is satisfied. In Formula (1), A represents at least one metal element selected from the group consisting of Sr, Ba, Ca, and Pb, and x satisfies 1.5≤x≤8.0.

AFe.sub.(12-x)Al.sub.xO.sub.19  Formula(1)

The present invention relates to: layered gallium arsenide (GaAs), which is more particularly layered GaAs, which, unlike the conventional bulk GaAs, has a two-dimensional crystal structure, has the ability to be easily exfoliated into nanosheets, and exhibits excellent electrical properties by having a structure that enables easy charge transport in the in-plane direction; a method of preparing the same; and a GaAs nanosheet exfoliated from the same.

Described herein are processes for preparation of a carbon foam material, the processes including the steps of heating in a microwave heating apparatus a mixture including a coal material and at least one additional agent. The additional agent can be a flux agent such a carbohydrate syrup, a secondary flux agent, a lignocellulosic waste material, a conductive carbon compound, a solvent, and combinations thereof. Also described are processes for calcining a carbon foam material in a furnace, a microwave heating apparatus, or an inductive field heater. The described calcining process can impart electrical conductivity and mechanical strength to carbon foams. Also described are carbon foam materials, calcined carbon foams, and composite materials. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure.

The present disclosure relates to a process for producing sheets of a composite material comprising a graphene film arranged on an amorphous carbon substrate, the process comprising the steps of: a) providing a lignin source and an aqueous solution to form a composition, b) depositing the composition on a metal surface, c) heating the composition on the metal surface to form the composite material.

Provided are a method for directly preparing expanded graphite or graphene under normal temperature and normal pressure, a graphene material, and a product. The method comprises the following specific steps: firstly dispersing graphite in an acidic medium containing an oxidizing agent, and then enabling obtained suspension liquid to stand under normal temperature and normal pressure, thus obtaining expanded graphite. The method does not involve any high-temperature high-pressure reaction process, is safe in operation, low in energy consumption and high in efficiency, and is environmentally-friendly. Obtained expanded graphite can realize 50-1500 times of volume expansion, and an sp2 hybridization structure of a graphene sheet layer is basically not damaged; and the obtained expanded graphite can be widely applied to the fields of energy storage, heat management, photoelectronic devices, solar cells, anti-corrosive materials, various composite materials, and the like. The prepared expanded graphite can also be used as a precursor for preparing high-quality graphene, and the high-quality graphene basically containing no defects can be obtained by peeling off the expanded graphite.