The present invention discloses a graphene composite material and a preparation method thereof. By adding pleated graphene oxide microspheres and a catalyst to a precursor, the pleated graphene oxide microspheres are allowed to be highly dispersed and gradually disassociated into single-layer graphene oxide sheets during the process of polycondensation, the partially esterified molecules react with the hydroxyl and carboxyl group on the surface of graphene oxide sheets to form a chemical bond, and the graphene oxide is thermally reduced, to finally obtain a composite material comprising PET and graphene sheets having PET grated to the surface.

The present disclosure provides a composite material. The composite material includes 20 to 40 weight percent (wt. %) of a polymerizable component; 6 to 40 wt. % of ceramic fibers; and 30 to 70 wt. % of nanoclusters. Each of the ceramic fibers has a diameter and a length, the ceramic fibers having an arithmetic mean diameter of 0.3 micrometers to 5 micrometers, and the length of fifty percent of the ceramic fibers (based on a total number of the ceramic fibers) is at least 10 micrometers and the length of ninety percent of the ceramic fibers is no greater than 500 micrometers. The present disclosure also provides a method of making the composite material. The method includes obtaining components and admixing the components to form a composite material. Further, the present disclosure provides a method of using a composite material including placing a composite material near or on a tooth surface, changing the shape of the composite material near or on a tooth surface, and hardening the composite material. In addition, the present disclosure provides dental products and kits. Hardened composite materials can exhibit high strength.

Disclosed a preparation method of a green, biodegradable, and multifunctional collagen-based nanocomposite film, and overcomes the problems of difficult biodegradation, poor barrier property, and single function of food packaging materials in the existing technologies. The present invention includes the following steps: adding silicate nanosheet into deionized water for ultrasonic dispersion; then adding polyphenolic acid into the mixture, wherein a mass ratio of the polyphenolic acid to the silicate nanosheet is 1:(0.2˜1); and adjusting the pH value to 3.0˜4.0 to obtain a solution A; adding collagen with a concentration of 5 g/L into an acetic acid solution, and fully dissolving the collagen to obtain a solution B; isovolumetrically mixing the solution A with the solution B, stirring at room temperature, and adjusting the pH value to 4.5˜5.5 to obtain a casting solution; and pouring the casting solution into a polytetrafluoroethylene mold, and naturally drying to obtain a nanocomposite film.

The present invention provides methods for uniform growth of nanostructures such as nanotubes (e.g., carbon nanotubes) on the surface of a substrate, wherein the long axes of the nanostructures may be substantially aligned. The nanostructures may be further processed for use in various applications, such as composite materials. For example, a set of aligned nanostructures may be formed and transferred, either in bulk or to another surface, to another material to enhance the properties of the material. In some cases, the nanostructures may enhance the mechanical properties of a material, for example, providing mechanical reinforcement at an interface between two materials or plies. In some cases, the nanostructures may enhance thermal and/or electronic properties of a material. The present invention also provides systems and methods for growth of nanostructures, including batch processes and continuous processes.

The present invention relates to a process for the production of naso-fibrillar cellulose gels by providing cellulose fibres and at least one filler and/or pigment; combining the cellulose fibres and the at least one filler and/or pigment; and fibrillating the cellulose fibres in the presence of the at least one filler and/or pigment until a gel is formed, as well as the nano-fibrillar cellulose gel obtained by this process and uses thereof.

A nanoparticle or agglomerate which contains connected multi-walled spherical fullerenes coated in layers of graphite. In different embodiments, the nanoparticles and agglomerates have different combinations of: a high mass fraction compared to other carbon allotropes present, a low concentration of defects, a low concentration of elemental impurities, a high Brunauer, Emmett and Teller (BET) specific surface area, and/or a high electrical conductivity. Methods are provided to produce the nanoparticles and agglomerates at a high production rate without using catalysts.

It is provided a phyllosilicate having a layered structure in the form of platelets and comprising an intercalating agent between the platelets, wherein the intercalating agent is a polyester of a molecular weight of 274 to 30,000 g/mol, and wherein the phyllosilicate is other than a phyllosilicate modified through ionic interchange. It is also provides a polymer nanocomposite comprising a polyethylene terephthalate (PET) polymer an the phyllosilicate mentioned above, as well as preparation processes for the preparation of the intercalated phyllosilicate and the PET nanocomposite. The PET nanocomposite is particularly useful for packaging, particularly for food and drink packaging.

Branched aramid nanofibers (ANFs) can be made by controlled chemical splitting of micro and macroscale aramid fiber by adjusting the reaction media containing aprotic component, protic component and a base. Branched ANFs have uniform size distribution of diameters in the nanoscale regime (below 200 nm) and high yield exceeding 95% of the nanofibers with this diameter. The method affords preparation of branched ANFs with 3-20 branches per one nanofiber and high aspect ratio. Branched ANFs form hydrogel or aerogels with highly porous 3D percolating networks (3DPNs) frameworks that are made into different shapes. Polymers and nanomaterials are impregnated into the 3DPNs through several methods. Gelation of branched ANFs facilitates layer-by-layer deposition in a process described as gelation assisted layer-by-layer deposition (gaLBL). A method of manufacturing battery components including ion conducting membranes, separators, anodes, and cathodes is described. The method of manufacturing of materials with high mechanical performance based on branched ANFs and 3DPNs from them is disclosed.

The present invention belongs to the technical field of organic supermolecules, and specifically discloses a 3,4-ethylenedioxythiophene (EDOT) polymer capable of supramolecular assembly with carbon-based materials, and a preparation method thereof The polymer of the present invention is a polymer with 3,4-ethylenedioxythiophene-2-acetylene as the main chain and alkoxy as the side chain. The polymer is prepared as follows: subjecting EDOT to bromination, to give 2,5-dibromo-3,4-ethylenedioxythiophene; then reacting 2,5-dibromo-3,4-ethylenedioxythiophene and trimethylsilyl acetylene (TMSA) to give bis(trimethylsilyl)-3,4-ethylenedioxythiophene; removing trimethylsilyl (TMS) protecting groups from the bis(trimethylsilyl)-3,4-ethylenedioxythiophene, and subjecting the obtained compound and 2,5-dibromo-3,4-ethylenedioxythiophene to Sonogashira coupling to give an EDOT polymer. The polymer of the present invention can form a supramolecular assembly system with carbon nanotubes (CMTs), which involves 71-71 adsorption of the main chain and entanglement of the side chain.

Methods of forming composite materials, which may include filament winding two or more carbon nanotube yarns to form one or more material layers, contacting the yarns with a resin, and applying one or more stretching forces to the material layers. Composite materials also are provided.