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; 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: 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: 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 present invention provides a polarized electrode 12 containing mixed activated carbon composed of at least two activated carbons with different specific surface areas, and the specific surface area of the mixed activated carbon is not less than 900 m2/g and less than 1900 m2/g. By setting the specific surface area of the mixed activated carbon to less than 1900 m2/g, the resistance reduction ratio of the polarized electrode 12 rapidly increases.

Abstract: The present invention provides an evaporated fuel gas adsorbent, an evaporated fuel gas trapping apparatus that uses the adsorbent, an activated carbon, and a process for producing the activated carbon. The evaporated fuel gas adsorbent is capable of improving adsorptivity and desorptivity by reliably preventing a temperature rise and a temperature fall caused by heat generated in response to the adsorption and desorption of evaporated fuel gas, is capable of achieving a size reduction of the device, and is capable of being easily produced. The activated carbon has high mechanical strength and high abrasive resistance, has many pores suitable to adsorb an organic solvent, especially, evaporated fuel gas, and has a high packing density. The activated-carbon producing process is industrially advantageous.

Abstract: The invention aims at providing a mercury adsorbent which is optimized in base activated carbon, sulfur amount carried, and heat treatment conditions, and is enhanced in mercury adsorption performance, and a process for producing the adsorbent, which can be put into industrial practice advantageously. The aim is attained by a mercury adsorbent made up of sulfur-carried activated carbon, with which sulfur is carried on activated carbon and which exhibits a sulfur peak top of the temperature of sulfur desorption at 534° C. to 537° C. in a calorimetric curve measured by a differential scanning calorimeter at a temperature rise rate of 10° C./minute under a nitrogen atmosphere, and a process for production of the adsorbent.

Abstract: The present invention provides a polarized electrode 12 containing mixed activated carbon composed of at least two activated carbons with different specific surface areas, and the specific surface area of the mixed activated carbon is not less than 900 m2/g and less than 1900 m2/g. By setting the specific surface area of the mixed activated carbon to less than 1900 m2/g, the resistance reduction ratio of the polarized electrode 12 rapidly increases.

Abstract: The present invention provides an evaporated fuel gas adsorbent, an evaporated fuel gas trapping apparatus that uses the adsorbent, an activated carbon, and a process for producing the activated carbon. The evaporated fuel gas adsorbent is capable of improving adsorptivity and desorptivity by reliably preventing a temperature rise and a temperature fall caused by heat generated in response to the adsorption and desorption of evaporated fuel gas, is capable of achieving a size reduction of the device, and is capable of being easily produced. The activated carbon has high mechanical strength and high abrasive resistance, has many pores suitable to adsorb an organic solvent, especially, evaporated fuel gas, and has a high packing density. The activated-carbon producing process is industrially advantageous.

Abstract: A high-density evaporated fuel gas adsorbent and process for forming such capable of preventing temperature rise and temperature fall caused with adsorption and desorption of an evaporated fuel gas, capable of stably maintaining adsorbing and desorbing properties of the adsorbent, and capable of preventing a heat storage component from leaking out therefrom. The adsorbent is formed by mixing together microcapsules in each of which a substance that absorbs or releases heat in response to phase change is encased and activated carbon in which pore volume in an average pore diameter of 50 nm to 1000 nm is 0.3 mL/g or more and in which half-value width of a D-band peak in the vicinity of 1360 cm?1 and half-value width of a G-band peak in the vicinity of 1580 cm?1 are both equal to 100 cm?1 or more in a Raman spectroscopic analysis, and by molding these integrally.

Abstract: The present invention provides an activated carbon produced by a process, which includes: activating a carbonaceous material, to obtain an activated carbonaceous material; and contacting the activated carbonaceous material with an acid. Another embodiment of the present invention provides an electrode for an electric double-layer capacitor, which includes the above-described activated carbon. Another embodiment of the present invention provides a filter, which includes the above-described activated carbon. Another embodiment of the present invention provides a shaped article, which includes the above-described activated carbon. Another embodiment of the present invention provides a method for producing activated carbon, which includes activating a carbonaceous material, to obtain an activated carbonaceous material; and contacting the activated carbonaceous material with an acid, to obtain the activated carbon.