A method for preparation of mesoporous nitrogen-doped carbon includes forming a composition by solubilizing a nitrogen-containing polymer in an aqueous solution of ZnCl.sub.2 and drying the aqueous solution, the method further includes heating the composition after drying to a temperature sufficiently high to carbonize the nitrogen-containing polymer to form the mesoporous nitrogen-doped carbon.

A method for preparation of mesoporous nitrogen-doped carbon includes forming a composition by solubilizing a nitrogen-containing polymer in an aqueous solution of ZnCl.sub.2 and drying the aqueous solution, the method further includes heating the composition after drying to a temperature sufficiently high to carbonize the nitrogen-containing polymer to form the mesoporous nitrogen-doped carbon.

The present invention relates to a carbonaceous material having a silicon element content of less than 200 ppm, a powder conductivity of 10.0 to 22.0 S/cm, a total amount of surface functional groups of 0.22 to 0.36 meq/g, and a pore volume of 0.10 to 0.20 cm.sup.3/g in terms of pores having a pore size of not less than 4 nm as measured by a BJH method.

An impregnation liquid is provided, which includes (A) phenolic resin, (B) diazonaphthoquinone-based compound or a derivative thereof, (C) ionic compound, and (D) organic solvent. The weight of (A) phenolic resin and the weight of (B) diazonaphthoquinone-based compound or a derivative thereof have a ratio of 0.2:0.8 to 0.9:0.1, and the weight of (C) ionic compound and the total weight of (A) phenolic resin and (B) diazonaphthoquinone-based compound or a derivative thereof have a ratio of 0.2:1 to 1.4:1. The impregnation liquid can be used to form an activated carbon layer to wrap and to be directly in contact with the surface of a mesh.

An impregnation liquid is provided, which includes (A) phenolic resin, (B) diazonaphthoquinone-based compound or a derivative thereof, (C) ionic compound, and (D) organic solvent. The weight of (A) phenolic resin and the weight of (B) diazonaphthoquinone-based compound or a derivative thereof have a ratio of 0.2:0.8 to 0.9:0.1, and the weight of (C) ionic compound and the total weight of (A) phenolic resin and (B) diazonaphthoquinone-based compound or a derivative thereof have a ratio of 0.2:1 to 1.4:1. The impregnation liquid can be used to form an activated carbon layer to wrap and to be directly in contact with the surface of a mesh.

The present invention covers a novel method for creating an adsorbent and the resulting novel adsorbent. The method may be used to remove pollutants/unwanted chemicals from water, air, other gases, biological fluids (such as blood, urine, lipids, protein fluids), and other fluids (such as fuel). The adsorbent may be used to remove heavy metals (for example, lead), organic pollutants, inorganic non-meal pollutants (for example, nitrates and bromates). Accordingly, the current invention has many applications including but not limited to water treatment, wastewater treatment, biomedical fluid treatments, gas cleanup, and fuel (oil, gas) cleanup.

The present invention covers a novel method for creating an adsorbent and the resulting novel adsorbent. The method may be used to remove pollutants/unwanted chemicals from water, air, other gases, biological fluids (such as blood, urine, lipids, protein fluids), and other fluids (such as fuel). The adsorbent may be used to remove heavy metals (for example, lead), organic pollutants, inorganic non-meal pollutants (for example, nitrates and bromates). Accordingly, the current invention has many applications including but not limited to water treatment, wastewater treatment, biomedical fluid treatments, gas cleanup, and fuel (oil, gas) cleanup.

A composition and method for fabricating graphitic nanocomposites in solid state matrices is presented. The process for fabricating graphitic nanocomposites in solid state matrices may include selecting one or a mixture of specific graphitic nanomaterials. The graphitic nanomaterial(s) may be functionalizing with a moiety similar to the building blocks of the solid state matrices. The functionalized graphitic nanomaterials are mixed with the building blocks of the solid state matrices. The mixture may be cured, which causes in situ formation of the sol-gel solid state matrices that entraps and/or covalently links with the graphitic nanomaterials during the network growing process. This process allows the nanomaterials to be introduced into the matrices homogeneously without forming large aggregations.

Composite carbon particles including a porous carbon material and a silicon component, the composite carbon particle having an average aspect ratio of 1.25 or less, and a ratio (I.sub.Si/I.sub.G) of a peak intensity (I.sub.Si) in the vicinity of 470 cm.sup.−1 to a peak intensity (I.sub.G) in the vicinity of 1580 cm.sup.−1 as measured by Raman spectroscopy of 0.30 or less, wherein the porous carbon material satisfies V.sub.1/V.sub.0>0.80 and V.sub.2/V.sub.0<0.10, when a total pore volume at a maximum value of a relative pressure P/P.sub.0 is defined as V.sub.0 and P.sub.0 is a saturated vapor pressure, a cumulative pore volume at a relative pressure P/P.sub.0=0.1 is defined as V.sub.1, a cumulative pore volume at a relative pressure P/P.sub.0=10.sup.−7 is defined as V.sub.2 in a nitrogen adsorption test, and has a BET specific surface area of 800 m.sup.2/g or more.

A method of producing a porous carbon is provided that can change type of functional groups, amount of functional groups, or ratio of functional groups while inhibiting its pore structure from changing. A method of producing a porous carbon includes: a first step of carbonizing a material containing a carbon source and a template source, to prepare a carbonized product; and a second step of immersing the carbonized product into a template removing solution, to remove a template from the carbonized product, and the method is characterized by changing at least two or more of the following conditions: type of the material, ratio of the carbon source and the template source, size of the template, and type of the template removal solution, to thereby control type, amount, or ratio of functional groups that are present in the porous carbon.