Patent classifications
C01B32/354
MOLDED ADSORBENT AND WATER PURIFICATION CARTRIDGE
To improve a performance for removing soluble lead and finely particulate lead. A molded adsorbent (1) includes an adsorption material (3) and a fibrous binder (5). The adsorption material (3) contains activated carbon (3A) and zeolite (3B). A central particle size D50 of the activated carbon (3A) is 27 μm or more and 35 μm or less, a central particle size D50 of the zeolite (3B) is 24 μm or more and 31 μm or less, and a content rate of the zeolite (3B) is 10 mass % or more and 70.5 mass % or less.
Magnetic composite containing polyethylenimine functionalized actived carbon and methods thereof
A polymer/activated carbon composite made up of a branched polyethylenimine and magnetic cores involving Fe.sub.3O.sub.4 disposed activated carbon. The magnetic cores have activated carbonyl groups on the surface. A process for removing organic dyes, such as methyl red, as well as heavy metal ions from a polluted aqueous solution or an industrial wastewater utilizing the composite is introduced. A method of synthesizing the polymer/activated carbon composites is also specified.
ELECTRODES FOR ELECTROCHEMICAL CAPACITORS BASED ON SURFACE-MODIFIED CARBON
A process for preparing surface-modified carbon, comprising adding carbon material to a solution of a reaction product of primary aromatic amine and excess molar amount of nitrite source, and recovering surface-modified carbon bearing redox-active sites. Surface-modified carbon material, electrodes and capacitors based thereon are also provided.
METHOD OF RECYCLING CARBON TO A FEEDSTOCK GAS REACTOR
A method of using a feedstock gas reactor is described. A hydrocarbon, such as methane, is chemical decomposed in the feedstock gas reactor using heat of combustion generated from the combustion of a combustible gas. A mixed product stream is extracted from the feedstock gas reactor. The mixed product stream comprises hydrogen, carbon, and water. At least a portion of the one or more combustion product gases are vented from the combustion chamber. At least some of the carbon is activated using the vented one or more combustion product gases. At least some of the activated carbon is recycled to the feedstock gas reactor.
Reactor, System and Method for Carbon-Based Material Post-Modification
A carbon-based material post-modification reactor includes: a feeding port located upstream from the carbon-based material post-modification reactor and adapted to feed a carbon-based raw material into the reactor; a discharging port located downstream from the carbon-based material post-modification reactor and adapted to output a modified carbon-based material; and a screw conveying device disposed in the reactor to simultaneously convey and turn over the carbon-based raw material in the reactor, between the feeding port and the discharging port; and an intake device for inputting ozone gas to the interior of the carbon-based material post-modification reactor. The screw conveying device includes a shaft portion, reverse inner spiral blade group and forward outer spiral blade group. The screw conveying device simultaneously conveys forward, conveys reversely, and turns over the carbon-based raw material in the carbon-based material post-modification reactor, thereby enhancing the performance of post-modification reaction.
Sulfur-carbon composite and method for preparing same
A method for preparing a sulfur-carbon composite including: (a) stirring a porous carbon material in a solvent mixture including a carbonate-based compound and a volatile solvent and then drying; and (b) mixing the dried porous carbon material with sulfur and then depositing the sulfur in and on the porous carbon material by a heat melting method. A method for preparing a sulfur-carbon composite including: (a) mixing and stirring a porous carbon material and sulfur in a solvent mixture including a carbonate-based compound and a volatile solvent and then drying; and (b) depositing the sulfur in and on the porous carbon material by a heat melting method. In the sulfur-carbon composite, sulfur present in and on the porous carbon material, a proportion of β-monoclinic sulfur phase to sulfur contained in the sulfur-carbon composite is 90% or more based on a total molar ratio of sulfur.
Apparatus for removing chemotherapy compounds from blood
A filter apparatus for removing small molecule chemotherapy agents from blood is provided. The filter apparatus comprises a housing with an extraction media comprised of polymer coated carbon cores. Also provided are methods of treating a subject with cancer of an organ or region comprising administering a chemotherapeutic agent to the organ or region, collecting blood laded with chemotherapeutic agent from the isolated organ, filtering the blood laden with chemotherapeutic agent to reduce the chemotherapeutic agent in the blood and returning the blood to the subject.
Apparatus for removing chemotherapy compounds from blood
A filter apparatus for removing small molecule chemotherapy agents from blood is provided. The filter apparatus comprises a housing with an extraction media comprised of polymer coated carbon cores. Also provided are methods of treating a subject with cancer of an organ or region comprising administering a chemotherapeutic agent to the organ or region, collecting blood laded with chemotherapeutic agent from the isolated organ, filtering the blood laden with chemotherapeutic agent to reduce the chemotherapeutic agent in the blood and returning the blood to the subject.
Carbonaceous material and method for producing same
The present invention relates to a carbonaceous material which is derived from a plant, having a specific surface area of 1800 to 3000 m.sup.2/g as measured by a BET method, a hydrogen element content of 0.42% by mass or less and an oxygen element content of 1.5% by mass or less.
CARBONACEOUS MATERIAL AND METHOD FOR PRODUCING SAME, WATER PURIFICATION FILTER, AND WATER PURIFIER
One aspect of the present invention relates to a carbonaceous material having a BET specific surface area calculated from a nitrogen adsorption isotherm by a BET method, of 750 m.sup.2/g or more and 1000 m.sup.2/g or less, a ratio of a pore volume of pores of 0.3875 to 0.9125 nm calculated from the nitrogen adsorption isotherm by a HK method to a total pore volume calculated from the nitrogen adsorption isotherm by the HK method, of 80% or more, and an average pore diameter obtained by the following formula using the BET specific surface area and the total pore volume calculated from the nitrogen adsorption isotherm by the HK method, of 1.614 nm or less: D=4000×V/S (wherein D represents the average pore diameter (nm), V represents the total pore volume (mL/g), and S represents the specific surface area (m.sup.2/g)).