Abstract: One aspect of the present invention relates to a carbonaceous material that has a benzene adsorption amount of 30 to 60%, a vitamin B12 adsorption amount of more than 50.0 mg/g, and a micropore volume of mesopores of 0.13 to 0.30 cm3/g as calculated from a nitrogen adsorption isotherm by a BJH method.

Abstract: A carbonaceous material for electric double-layer capacitors that is based on a plant-derived carbon precursor, in which carbonaceous material: a BET specific surface area is 1,900 to 2,500 m2/g; an average pore size is 2.2 to 2.6 nm as determined by a nitrogen adsorption method; a volume of micropores having a pore size of 2 nm or smaller is 0.84 to 1.30 cm3/g as determined by the MP method; a ratio of a volume of micropores having a pore size of 1 to 2 nm with respect to the volume of the micropores having a pore size of 2 nm or smaller is 25 to 50% as determined by the MP method; and a volume of mesopores having a pore size of 2 to 50 nm is 0.16 to 0.4 cm3/g as determined by the BJH method; and a method of producing same.

Abstract: Provided is a mercury adsorbent that can efficiently adsorb and remove mercury and/or a mercury compound contained in a liquid hydrocarbon and can suppress corrosive action even when used for a long time. The mercury adsorbent comprises an activated carbon including a mineral acid supported thereon, the activated carbon having a specific surface area of 1000 m2/g or larger and a volume of micropores of 80 cm3/g or larger, each of the micropores having a pore radius of 8 ? or smaller, and the mercury adsorbent has a moisture content of from 0.1 to 3 wt %.

Abstract: A carbonaceous material for electric double-layer capacitors that is based on a plant-derived carbon precursor, in which carbonaceous material: a BET specific surface area is 1,900 to 2,500 m2/g; an average pore size is 2.2 to 2.6 nm as determined by a nitrogen adsorption method; a volume of micropores having a pore size of 2 nm or smaller is 0.84 to 1.30 cm3/g as determined by the MP method; a ratio of a volume of micropores having a pore size of 1 to 2 nm with respect to the volume of the micropores having a pore size of 2 nm or smaller is 25 to 50% as determined by the MP method; and a volume of mesopores having a pore size of 2 to 50 nm is 0.16 to 0.4 cm3/g as determined by the BJH method; and a method of producing same.

Abstract: A carbonaceous material for electric double-layer capacitors that is based on a plant-derived carbon precursor, in which carbonaceous material: a BET specific surface area is 1,900 to 2,500 m2/g; an average pore size is 2.2 to 2.6 nm as determined by a nitrogen adsorption method; a volume of micropores having a pore size of 2 nm or smaller is 0.84 to 1.30 cm3/g as determined by the MP method; a ratio of a volume of micropores having a pore size of 1 to 2 nm with respect to the volume of the micropores having a pore size of 2 nm or smaller is 25 to 50% as determined by the MP method; and a volume of mesopores having a pore size of 2 to 50 nm is 0.16 to 0.4 cm3/g as determined by the BJH method.

Abstract: The object of the present invention is to provide a carbonaceous material which is obtainable from plant-derived char and has a decreased specific surface area. Further, the object of the present invention is to provide a non-aqueous electrolyte secondary battery having excellent dedoping capacity, non-dedoping capacity, and charge-discharge efficiency. The object can be solved by a carbonaceous material for non-aqueous electrolyte secondary batteries characterized in that the carbonaceous material is obtained by heat-treating plant-derived char which is demineralized in gas-phase, and carbon precursor or volatile organic compound under a non-oxidizing gas atmosphere; and a specific surface area determined by a BET method is 10 m2/g or less.

Abstract: A carbonaceous material for electric double-layer capacitors that is based on a plant-derived carbon precursor, in which carbonaceous material: a BET specific surface area is 1,900 to 2,500 m2/g; an average pore size is 2.2 to 2.6 nm as determined by a nitrogen adsorption method; a volume of micropores having a pore size of 2 nm or smaller is 0.84 to 1.30 cm3/g as determined by the MP method; a ratio of a volume of micropores having a pore size of 1 to 2 nm with respect to the volume of the micropores having a pore size of 2 nm or smaller is 25 to 50% as determined by the MP method; and a volume of mesopores having a pore size of 2 to 50 nm is 0.16 to 0.4 cm3/g as determined by the BJH method.

Abstract: A porous carbon material for electrodes of energy storage devices comprising: a porous carbon material; 0.5 to 5 parts by mass of an insulating material having a boiling point of 150° C. or more based on 100 parts by mass of the porous carbon material; and 0.25 to 15 parts by mass of a conductive additive based on 100 parts by mass of the insulating material, wherein the insulating material and the conductive additive are carried on the porous carbon material in combination, and the porous carbon material has a BET specific surface area of 1300 to 2050 m2/g.

Abstract: The object of the present invention is to provide a carbonaceous material which is obtainable from plant-derived char and has a decreased specific surface area. Further, the object of the present invention is to provide a non-aqueous electrolyte secondary battery having excellent dedoping capacity, non-dedoping capacity, and charge-discharge efficiency. The object can be solved by a carbonaceous material for non-aqueous electrolyte secondary batteries characterized in that the carbonaceous material is obtained by heat-treating plant-derived char which is demineralized in gas-phase, and carbon precursor or volatile organic compound under a non-oxidizing gas atmosphere; and a specific surface area determined by a BET method is 10 m2/g or less.

Abstract: A porous carbon material for electrodes of energy storage devices comprising: a porous carbon material; 0.5 to 5 parts by mass of an insulating material having a boiling point of 150° C. or more based on 100 parts by mass of the porous carbon material; and 0.25 to 15 parts by mass of a conductive additive based on 100 parts by mass of the insulating material, wherein the insulating material and the conductive additive are carried on the porous carbon material in combination, and the porous carbon material has a BET specific surface area of 1300 to 2050 m2/g.

Abstract: The object of the present invention is to provide a manufacturing method of carbonaceous material for a negative electrode of lithium ion capacitors, wherein the carbonaceous material is obtained from plant-derived char as a source, potassium and iron are sufficiently removed, and an average particle diameter thereof is small; and a carbonaceous material for a negative electrode of lithium ion capacitors. The object can be solved by a method for manufacturing a carbonaceous material having an average diameter of 3 to 30 ?m, for a negative electrode of lithium ion capacitors comprising the steps of: (1) heating plant-derived char having an average particle diameter of 100 to 10000 ?m at 500° C. to 1250° C. under an inert gas atmosphere containing a halogen compound to demineralize in a gas-phase, (2) pulverizing a carbon precursor obtained by the demineralization in a gas-phase, (3) calcining the pulverized carbon precursor at less than 1100° C. under a non-oxidizing gas atmosphere.

Abstract: Provided is a manufacturing method of carbonaceous material for a negative electrode of non-aqueous electrolyte secondary batteries, wherein the carbonaceous material is obtained from plant-derived char as a source, potassium is sufficiently removed, and an average particle diameter thereof is small; and a carbonaceous material for a negative electrode of non-aqueous electrolyte secondary batteries. The method for manufacturing a carbonaceous material having an average particle diameter of 3 to 30 ?m, for a negative electrode of non-aqueous electrolyte secondary batteries includes the steps of: (1) heating plant-derived char having an average particle diameter of 100 to 10000 ?m at 500° C. to 1250° C. under an inert gas atmosphere containing halogen compound to demineralize in a gas-phase, (2) pulverizing a carbon precursor obtained by demineralization in a gas-phase, (3) calcining the pulverized carbon precursor at 1000° C. to 1600° C. under an non-oxidizing gas atmosphere.

Abstract: There is provided a carbon material for polarizable electrodes in which a heterocyclic aromatic compound is adsorbed on an activated carbon, wherein the heterocyclic aromatic compound comprises a five- or six-membered ring having two or more nitrogen atoms as ring-forming atoms; a ratio (N/C) of nitrogen atoms to carbon atoms in the heterocyclic aromatic compound is 0.4 or more; 1 to 35 parts by mass of the heterocyclic aromatic compound is adsorbed based on 100 parts by mass of the activated carbon; and the carbon material for polarizable electrodes has a benzene adsorption capacity of 25 to 75% by mass.

Abstract: The object of the present invention is to provide a manufacturing method of carbonaceous material for a negative electrode of non-aqueous electrolyte secondary batteries, wherein the carbonaceous material is obtained from plant-derived char as a source, potassium is sufficiently removed, and an average particle diameter thereof is small; and a carbonaceous material for a negative electrode of non-aqueous electrolyte secondary batteries. The object can be solved by a method for manufacturing a carbonaceous material having an average particle diameter of 3 to 30 ?m, for a negative electrode of non-aqueous electrolyte secondary batteries comprising the steps of: (1) heating plant-derived char having an average particle diameter of 100 to 10000 ?m at 500° C. to 1250° C. under an inert gas atmosphere containing halogen compound to demineralize in a gas-phase, (2) pulverizing a carbon precursor obtained by demineralization in a gas-phase, (3) calcining the pulverized carbon precursor at 1000° C. to 1600° C.

Abstract: There is provided a carbon material for polarizable electrodes in which a heterocyclic aromatic compound is adsorbed on an activated carbon, wherein the heterocyclic aromatic compound comprises a five- or six-membered ring having two or more nitrogen atoms as ring-forming atoms; a ratio (N/C) of nitrogen atoms to carbon atoms in the heterocyclic aromatic compound is 0.4 or more; 1 to 35 parts by mass of the heterocyclic aromatic compound is adsorbed based on 100 parts by mass of the activated carbon; and the carbon material for polarizable electrodes has a benzene adsorption capacity of 25 to 75% by mass.

Abstract: The object of the present invention is to provide a manufacturing method of carbonaceous material for a negative electrode of lithium ion capacitors, wherein the carbonaceous material is obtained from plant-derived char as a source, potassium and iron are sufficiently removed, and an average particle diameter thereof is small; and a carbonaceous material for a negative electrode of lithium ion capacitors. The object can be solved by a method for manufacturing a carbonaceous material having an average diameter of 3 to 30 ?m, for a negative electrode of lithium ion capacitors comprising the steps of: (1) heating plant-derived char having an average particle diameter of 100 to 10000 ?m at 500° C. to 1250° C. under an inert gas atmosphere containing a halogen compound to demineralize in a gas-phase, (2) pulverizing a carbon precursor obtained by the demineralization in a gas-phase, (3) calcining the pulverized carbon precursor at less than 1100° C. under a non-oxidizing gas atmosphere.

Abstract: The object of the present invention is to provide a carbonaceous material which is obtainable from plant-derived char and has a decreased specific surface area. Further, the object of the present invention is to provide a non-aqueous electrolyte secondary battery having excellent dedoping capacity (discharge capacity), non-dedoping capacity (irreversible capacity), and charge-discharge efficiency. The object can be solved by a carbonaceous material for non-aqueous electrolyte secondary batteries characterized in that the carbonaceous material is obtained by heat-treating plant-derived char which is demineralized in gas-phase, and carbon precursor (i.e. non-graphitizable carbon precursor, graphitizable carbon, or mixture thereof) or volatile organic compound under a non-oxidizing gas atmosphere; and a specific surface area determined by a BET method is 10 m2/g or less.

Abstract: A composite adsorbent which comprises a composite powder composed of a particulate compound, a plastic powder adhered to the compound, and at least one adsorptive substance selected from powdery, particulate and fibrous substances; a composite material adsorbent which comprises a particulate compound and at least one adsorptive substance selected from powdery, particulate and fibrous substances, both of which have the plastic powder adhered thereto; methods for producing composite adsorbents; a water purification material comprising a composite adsorbent; and a water purifier comprising a composite material. The composite adsorbent exhibits a reduced resistance when a liquid passes through it, and is excellent in performance capabilities for the removal of free chlorine, THM, a heavy metal and the like. The composite adsorbent also provides water transmitted through it with satisfactory clarity, and is less prone to cause discrepancies in performance capabilities between respective purifiers.

Abstract: A polarizing electrode for an electric double layer capacitor has good moldability and can achieving higher density of electrode and higher capacity, and an electric double layer capacitor employs the same. The electric double layer capacitor is made of an activated carbon obtained by activating a hard-to-graphitize material (for example, phenol resin) with water vapor, and the activated carbon has a median particle size within a range from 4 ?m to 8 ?m in the particle size distribution and at least a peak observed on the side of smaller particle size than the median particle size in the particle size distribution.

Abstract: A composite particulate article which comprises a particulate article and, carried thereon, a fine particulate compound entangled in a fibrillated fiber; a method for preparing the composite particulate article; a gas clarifying material comprising the composite particulate article; a water clarifying material comprising the composite particulate article; and a water clarifying device using the water clarifying material. The composite particulate article exhibits a reduced resistance to the passing of a gas or a liquid through it, without detriment to the performance capabilities inherent in the particulate article, and also satisfactorily exerts the specific performance capabilities of the fine particulate compound with respect to adsorption or a catalytic reaction.