Abstract: The present invention provides a novel cost efficient method for carbonizing lignocellulosic material to carbonized particles or agglomerates, preferably carbon powder. Also uses of said particles or agglomerates are disclosed.

Abstract: A material that can be used in a wide temperature range and a manufacturing method thereof are provided. A graphene compound has a substituted or unsubstituted chain group. The chain group has one or more ester groups or carboxyl groups and contains a Si atom. The chain group is bonded to a graphene layer through the Si atom. A method for forming a graphene compound includes a step of stirring graphene oxide and a Lewis base and a step of mixing a silicon compound having one or more ester groups or carboxyl groups into the mixed solution and stirring the obtained mixed solution. The Lewis base is butylamine, pentylamine, hexylamine, diethylamine, dipropylamine, dibutylamine, triethylamine, tripropylamine, or pyridine.

Abstract: Provided is a method of producing isolated graphene sheets directly from a carbon/graphite precursor. The method comprises: (a) providing a mass of aromatic molecules wherein the aromatic molecules are selected from petroleum heavy oil or pitch, coal tar pitch, a polynuclear hydrocarbon, or a combination thereof; (b) heat treating this mass and using chemical or mechanical means to form graphene domains dispersed in a disordered matrix of carbon or hydrocarbon molecules, wherein the graphene domains are each composed of from 1 to 30 planes of hexagonal carbon atoms or fused aromatic rings having a length or width from 5 nm to 20 ?m and an inter-graphene space between two planes of hexagonal carbon atoms or fused aromatic rings no less than 0.4 nm; and (c) separating and isolating the planes of hexagonal carbon atoms or fused aromatic rings to recover graphene sheets from the disordered matrix.

Abstract: Select embodiments of the present invention employ biological means to direct assemble CNT-based nanostructures, allowing for scaling to macrostructures for manufacture. In select embodiments of the present invention, a method is provided for assembling DNA-functionalized SWNTs by phosphodiester bonding catalyzed by ssDNA-ligase to form macroscopic CNT aggregates.

Abstract: A method of making stable aqueous dispersions and concentrates of cobalt oxide nanoparticles is described, wherein a reaction mixture comprising cobalt(II) ion, a carboxylic acid, a base, an oxidant and water is formed, and in which cobalt oxide nanoparticles are formed. Cobalt oxide nanoparticles ranging in average crystallite size from about 4 nm to 15 nm are described. The cobalt oxide nanoparticles may be isolated and redispersed to form stable, homogeneous, aqueous dispersions of cobalt oxide nanoparticles containing from about 1 to about 20 weight percent cobalt oxide.

Abstract: 2-dimensional carbon thin films are described, as well as their processes of preparation, and their specific uses. The 2-dimensional carbon thin films are fabricated by preparing an organic polymeric thin film precursor, which is then subjected to a carbonisation process to remove at least some of the non-carbon atoms. Using the disclosed process, 2-dimensional carbon thin films having improved dimensional characteristics can be reliably prepared, which presents clear advantages in applications which have until now been restricted to the use of 2-dimensional carbon thin films having less useful dimensions.

Abstract: A method comprising reacting an aluminum mineral polymorph or a gallium mineral polymorph with an acid at an aluminum metal to acid molar ratio or gallium metal to acid molar ratio sufficient to produce M13 nanoscale clusters, M nano-agglomerates, or a M13 slurry, wherein M is Al or Ga.

Abstract: Provided is a method for continuously preparing graphene oxide nanoplatelets by electrochemical treatment, comprising using a continuous graphite product, successively processing two step treatments, i.e. an electrochemical intercalation and an electrolytic oxidation stripping. The electrochemical intercalation is carried out in a concentrated acid, using a graphite material as an anode and energizing under a soaking condition such that acid radical ions enter into graphite interlamination under the drive of an electric field, to form an intercalated graphite continuous material with first-order or low-order intercalation. The electrolytic stripping is using the intercalated continuous graphite material as an anode, energizing in an aqueous electrolyte solution, and performing oxidation stripping.

Abstract: The present invention discloses a preparation method of a sulfonated two-dimensional titanium carbide nanosheet, which comprises the following steps of preparing two-dimensional titanium carbide by using aluminum atomic layers in hydrofluoric acid chemical stripping layer-shaped titanium aluminum carbide; preparing sulfanilic acid diazosalt; conducting a sulfonation reaction between the two-dimensional titanium carbide and the sulfanilic acid diazosalt to prepare the sulfonated two-dimensional titanium carbide nanosheet. The sulfonated two-dimensional titanium carbide nano material prepared through the present invention has good dispersity in water and common organic solvents, and a single-layer or few-layer sulfonated two-dimensional titanium carbide nanosheet with large size and high quality can be obtained after ultrasonic treatment is performed on a dispersion liquid.

Abstract: A polyimide film suitable for use in the fabrication of a graphite layer includes a polyimide derived from reaction of diamine monomers with dianhydride monomers, and a foaming agent incorporated in the polyimide. Moreover, a process of fabricating a graphite film includes providing a polyamic acid solution formed by reaction of diamine monomers with dianhydride monomers, incorporating a foaming agent into the polyamic acid solution, forming a polyimide film from the polyamic acid solution, applying a first thermal treatment so that the polyimide film is carbonized to form a carbon film, and applying a second thermal treatment so that the carbon film is converted to a graphite film.

Abstract: The present invention relates to a process for producing an aqueous suspension of precipitated calcium carbonate, an aqueous suspension of precipitated calcium carbonate and a precipitated calcium carbonate obtained by the process, a process comprising the precipitated calcium carbonate and its use.

Abstract: Compositions are provided that can include nanoscale particles including metal cations such as cerium having an average particle size of less than 10 nm. The nanoscale particles can include cerium and oxygen. Methods for forming nanoparticles are provided. The methods can include exposing a metal cation within a solution to radiation to form metal nanoparticles that can include metal cations. The methods can include exposing a cerium salt solution to radiation to form the nanoparticles. The methods can include exposing solvated metal cations to radiation to precipitate nanoparticles that include metal cations such as Ce. The methods can include exposing the homogeneous solution to radiation to precipitate nanoparticles. The methods can include: providing an aqueous solution comprising metal cations; and increasing the pH of the aqueous solution with radiation to form nanoparticles that include metal cations. Nanoparticle generators are provided.

Abstract: The disclosure discloses an apparatus for continuous preparation of carbon nanotubes, comprising a main reactor, a separator and a return pipe, wherein the main reactor comprises a raw gas inlet, a return feed inlet, a protective gas inlet and a reaction material outlet; the separator is fluid communicated with the reaction material outlet of the main reactor at a top of the separator; a magnetic separating unit is arranged in the top of the separator at a side proximal to the main reactor; a product outlet and a material recycling port are arranged at a bottom of the separator respectively; the product outlet is located at a side distal to the main reactor; the recycling port is located at a side proximal to the main reactor; one end of the return pipe is fluid communicated with the material recycling port of the separator, and the other end is fluid communicated with the return feed inlet of the main reactor; the apparatus further comprises a tail gas outlet.

Abstract: The method of synthesizing magnetite/maghemite core/shell nanoparticles is a modified co-precipitation method for producing iron oxide (Fe3O4/?-Fe2O3) nanoparticles that allows for production of the Fe3O4/?-Fe2O3 core/shell nanoparticles with a desired shell thickness ranging between about 1 nm to 5 nm for biomedical and data storage applications. Aqueous solutions of ferric and ferrous salts are mixed at room temperature and pH of the mixture is raised to 10. The mixture is then heated at 80° C. for different lengths of time at atmospheric pressure to adjust particle size, and the precipitate is dried at 120° C. in vacuum. Oxidation in an oxygen atmosphere for different lengths of time is used to adjust the thickness of the ?-Fe2O3 shell.

Abstract: The problem addressed by the present invention is to provide an apparatus for preparing ultrathin graphene pieces capable of preparing ultrathin graphene pieces in which less than 10 pieces of graphene are overlapped in large quantities, a method for preparing ultrathin graphene pieces capable of preparing the ultrathin graphene pieces with high yield, an ultrathin graphene piece in which less than 10 pieces of graphene are overlapped, a capacitor having high performance by using the ultrathin graphene piece as an electrode, and an efficient method of manufacturing the capacitor.

Abstract: The present invention relates to activated carbon sorbents including nitrogen. In various embodiments, the present invention provides an activated carbon sorbent including a halogen- or halide-promoted activated carbon, the activated carbon sorbent particles including nitrogen in a surface layer of the sorbent particles. In various embodiments, the present invention provides a method of reducing the pollutant content in a pollutant-containing gas using the activated carbon sorbent. In various embodiments, the activated carbon sorbent can remove mercury from a mercury-containing gas that includes sulfur(VI) such as SO3 more efficiently than other sorbents.

Abstract: The present invention relates to a method for preparing graphene which comprises subjecting expanded graphite to high speed homogenization to prepare a feed solution and then subjecting the same to high pressure homogenization, thereby increasing the degree of dispersion of expanded graphite in the feed solution and so improving the efficiency of high pressure homogenization. Therefore, the present method has features that the efficiency of graphene preparation is excellent and the size of graphene to be prepared is uniform, compared with a conventional process.

Abstract: Provided are compositions for and methods of producing hydrogen. For example, the compositions comprise nanocrystals, a catalyst, a source of electrons, and an aqueous medium. The nanocrystals, catalyst, aqueous medium, and, optionally, the source of electrons are present as a mixture. The methods produce hydrogen by exposing the compositions to electromagnetic radiation (e.g., solar flux).

Abstract: A method for industrially manufacturing large-size graphene comprises following steps: (1) mixing graphite and concentrated sulfuric acid to obtain a mixed liquid, and ultrasonically treating the mixed liquid to obtain an upper layer of graphene and a lower layer of concentrated sulfuric acid liquid under condition that a chemical intercalation and a mechanical stripping were performed simultaneously; (2) separating the upper layer of graphene and the lower layer of concentrated sulfuric acid liquid; (3) the graphene separated in the step (2) being washed with water, filtered, and dried to obtain a large-size graphene. The method has the advantages of good peeling effect, great graphene size, repeated use of sulfuric acid as an intercalating agent, environment-friendliness, resource saving and wide industrial application prospect.

Abstract: The present disclosure relates to a process for the synthesis of highly crystalline carbon nanotubes (CNTs). Processes known in the art employ post-synthesis processes such as oxidation or hydrothermal treatment to produce CNTs with high crystallinity. The present disclosure produces highly crystalline CNTs at a low growth temperature and without hydrogen flow condition and without employing any post-production process. The process disclosed in the present disclosure produces CNTs having a crystallinity greater than 5 which makes them suitable for various industrial applications.