Abstract: A sheet-shaped member is provided and includes a porous carbon material including a material obtained from carbonization of a raw material including rice husk, the raw material having a silicon content of at least 5 wt %, the raw material is heat treated before carbonization, and the raw material is treated by an alkali treatment after carbonization to reduce the silicon content, the porous carbon material having a specific surface area of at least 10 m2/g as measured by the nitrogen BET method, a pore volume of at least 0.1 cm3/g as measured by the BJH method and MP method, and an R value of 1.

Abstract: A method includes producing a diiminopyrrole compound by mixing an aromatic 3-pyrroline compound, an iodinating agent, and ammonia based on Chemical Formula 1 below, in which ring A is an aromatic group:

Abstract: A porous carbon material having a value of a specific surface area by a nitrogen BET method of 1×102 m2/g or more, a volume of fine pores by a BJH method of 0.3 cm3/g or more, and a particle size of 75 ?m or more, alternatively, a porous carbon material having a value of a specific surface area by a nitrogen BET method of 1×102 m2/g or more, a total of volumes of fine pores having a diameter of from 1×10?9 m to 5×10?7 m, obtained by a non-localized density functional theory method, of 1.0 cm3/g or more, and a particle size of 75 ?m or more.

Abstract: Disclosed herein is a fungicide, including a porous carbon material and a silver member adhered to the porous carbon material, wherein a value of a specific surface area based on a nitrogen BET, namely Brunauer, Emmett, and Teller method is equal to or larger than 10 m2/g, and a volume of a fine pore based on a BJH, namely Barrett, Joyner, and Halenda method and an MP, namely Micro Pore method is equal to or larger than 0.1 cm3/g.

Abstract: A filter medium of the present invention includes a porous carbon material having a value of a specific surface area by a nitrogen BET method of 1×102 m2/g or more, a volume of fine pores by a BJH method of 0.3 cm3/g or more, and a particle size of 75 ?m or more, alternatively, a porous carbon material having a value of a specific surface area by a nitrogen BET method of 1×102 m2/g or more, a total of volumes of fine pores having a diameter of from 1×10?9 m to 5×10?7 m, obtained by a non-localized density functional theory method, of 1.0 cm3/g or more, and a particle size of 75 ?m or more.

Abstract: A porous carbon material composite formed of a porous carbon material and a functional material and equipped with high functionality. The porous carbon material composite is formed of (A) a porous carbon material obtainable from a plant-derived material having a silicon (Si) content of 5 wt % or higher as a raw material; and (B) a functional material adhered on the porous carbon material, and has a specific surface area of 10 m2/g or greater as determined by the nitrogen BET method and a pore volume of 0.1 cm3/g or greater as determined by the BJH method and MP method.

Abstract: A sheet-shaped member is provided and includes a porous carbon material including a material obtained from carbonization of a raw material including rice husk, the raw material having a silicon content of at least 5 wt %, the raw material is heat treated before carbonization, and the raw material is treated by an alkali treatment after carbonization to reduce the silicon content, the porous carbon material having a specific surface area of at least 10 m2/g as measured by the nitrogen BET method, a pore volume of at least 0.1 cm3/g as measured by the BJH method and MP method, and an R value of 1.

Abstract: A carbon-polymer complex is provided and includes a porous carbon material and a binder, wherein the porous carbon material includes a material obtained from carbonization of a raw material including rice husk, the raw material having a silicon content of at least 5 wt %, the raw material is heat treated before carbonization, and the raw material is treated by an alkali treatment after carbonization to reduce the silicon content, the porous carbon material having a specific surface area of at least 10 m2/g as measured by the nitrogen BET method, a pore volume of at least 0.1 cm3/g as measured by the BJH method and MP method, and an R value of 1.5 or greater, wherein the porous carbon material includes mesopores having pore sizes from 2 nm to 50 nm and obtained from the alkali treatment of the raw material after carbonization, the porous carbon material further includes macropores and micropores.

Abstract: An air-metal secondary battery has an electrode including a porous carbon material, wherein the porous carbon material has a specific surface area of 280 m2/g or more, preferably 700 m2/g or more, more preferably 1,500 m2/g or more, as determined by a nitrogen BET method, and the air-metal secondary battery has an average charging voltage of 4.4 V or less, preferably 4.3 V or less, more preferably 4.1 V or less.

Abstract: A porous carbon material wherein a particle diameter is 10 ?m or more but 1 cm or less; wherein a bulk specific gravity is 0.20 g/cm3 or more; and wherein a mesopore volume is 0.10 cm3/g or more.

Abstract: An image forming apparatus includes a linehead and a control unit. The linehead of an image forming apparatus includes a common ink chamber, a plurality of nozzles, an individual ink flow path, an ink supply path, a first piezoelectric actuator, and a second piezoelectric actuator. One end of the individual ink flow path is connected to the nozzle. The ink supply path is connected to the individual ink flow path and the common ink chamber. When putting the nozzle into a drying prevention state, the control unit deforms the first piezoelectric actuator in a direction in which a capacity of the individual ink flow path increases, to thereby draw an interface of ink to inside the nozzle. Further, the control unit deforms the second piezoelectric actuator, to thereby close the ink supply path.

Abstract: A porous carbon material composite formed of a porous carbon material and a functional material and equipped with high functionality. The porous carbon material composite is formed of (A) a porous carbon material obtainable from a plant-derived material having a silicon (Si) content of 5 wt % or higher as a raw material; and (B) a functional material adhered on the porous carbon material, and has a specific surface area of 10 m2/g or greater as determined by the nitrogen BET method and a pore volume of 0.1 cm3/g or greater as determined by the BJH method and MP method.

Abstract: A porous carbon material having a value of a specific surface area by a nitrogen BET method of 1×102 m2/g or more, a volume of fine pores by a BJH method of 0.3 cm3/g or more, and a particle size of 75 ?m or more, alternatively, a porous carbon material having a value of a specific surface area by a nitrogen BET method of 1×102 m2/g or more, a total of volumes of fine pores having a diameter of from 1×10?9 m to 5×10?7 m, obtained by a non-localized density functional theory method, of 1.0 cm3/g or more, and a particle size of 75 ?m or more.

Abstract: A carbon-polymer complex is provided and includes a porous carbon material and a binder, wherein the porous carbon material includes a material obtained from carbonization of a raw material including rice husk, the raw material having a silicon content of at least 5 wt %, the raw material is heat treated before carbonization, and the raw material is treated by an alkali treatment after carbonization to reduce the silicon content, the porous carbon material having a specific surface area of at least 10 m2/g as measured by the nitrogen BET method, a pore volume of at least 0.1 cm3/g as measured by the BJH method and MP method, and an R value of 1.5 or greater, wherein the porous carbon material includes mesopores having pore sizes from 2 nm to 50 nm and obtained from the alkali treatment of the raw material after carbonization, the porous carbon material further includes macropores and micropores.

Abstract: A porous carbon material comprising a material obtained from carbonization of a raw material including one or both of seaweed stem and straw, the raw material having a silicon content of at least 5 wt %, the raw material is heat treated before carbonization, and the raw material is treated by an alkali treatment after carbonization to reduce the silicon content, the porous carbon material having a value of specific surface area of at least 10 m2/g as measured by the nitrogen BET method, a pore volume of at least 0.1 cm3/g as measured by the BJH method and MP method, and an R value of 1.5 or greater, wherein the porous carbon material includes mesopores having pore sizes from 2 nm to 50 nm and obtained from the alkali treatment of the raw material after carbonization, the porous carbon material further includes macropores and micropores.

Abstract: A porous carbon material is provided. The porous carbon material having a value of specific surface area of at least 10 m2/g as measured by a nitrogen BET method, a pore volume of at least 0.1 cm3/g as measured by a BJH method and a MP method, and a R value of 1.5 or greater, wherein the R value is expressed as R=B/A, wherein A is an intensity at an intersection between a baseline of a diffraction peak of a (002) plane as obtained based on powdery X-ray diffractometry of the porous carbon material and a perpendicular line downwardly drawn from the diffraction peak of the (002) plane, and wherein B is an intensity of the diffraction peak of the (002) plane.

Abstract: Disclosed herein is a fungicide, including: a porous carbon material; and a silver member adhered to the porous carbon material, wherein a value of a specific surface area based on a nitrogen BET, namely Brunauer, Emmett, and Teller method is equal to or larger than 10 m2/g, and a volume of a fine pore based on a BJH, namely Barrett, Joyner, and Halenda method and an MP, namely Micro Pore method is equal to or larger than 0.1 cm3/g.

Abstract: By a process for producing a porous carbon material from a plant-derived material as a raw material, said process including carbonizing the plant-derived material at 800° C. to 1,400° C. and then applying a treatment with an acid or alkali, a porous carbon material having a value of specific surface area of at least 10 m2/g as measured by the nitrogen BET method, a silicon content of at most 1 wt % and a pore volume of at least 0.1 cm3/g is obtainable from a plant-derived material, which has a silicon content of at least 10 wt %, as a raw material. Also provided is a process for producing a porous carbon material equipped with excellent functionality so that the porous carbon material can be used, for example, as an anode material for batteries, an adsorbent, masks, adsorbing sheets, or carriers.

Abstract: An electrode material for a secondary cell includes a porous carbon material having an absolute value of a differential value of a mass using a temperature as a parameter exceeding 0 at 360° C. and being 0.016 or more at 290° C. provided by thermally analyzing a mixture of the porous carbon material and S8 sulfur at a mass ratio of 1:2.

Abstract: [Object] To provide an adsorbent, an adsorbent sheet, and a carbon/polymer composite for adsorbing a virus having further improved virus adsorption capability. [Solving Means] An adsorbent for adsorbing a virus according to the present invention has a specific surface area value as measured by the nitrogen BET method of 10 m2/g or more and a pore volume as measured by the BJH method of 0.1 cm3/g or more. An adsorbent sheet for adsorbing a virus according to the present invention includes a porous carbonaceous material having a specific surface area value as measured by the nitrogen BET method of 10 m2/g or more and a pore volume as measured by the BJH method of 0.1 cm3/g or more. A carbon/polymer composite for adsorbing a virus according to the present invention includes a porous carbonaceous material having a specific surface area value as measured by the nitrogen BET method of 10 m2/g or more and a pore volume as measured by the BJH method of 0.1 cm3/g or more; and a binder.