Abstract: A solid oxide fuel cell assembly (SOFC) and a method for making the SOFC are provided. An exemplary method includes forming a functionalized zeolite templated carbon (ZTC). The functionalized ZTC is formed by forming a CaX zeolite, depositing carbon in the CaX zeolite using a chemical vapor deposition (CVD) process to form a carbon/zeolite composite, treating the carbon/zeolite composite with a solution comprising hydrofluoric acid to form a ZTC, and treating the ZTC to add catalyst sites. The functionalized ZTC is incorporated into electrodes by forming a mixture of the functionalized ZTC with a calcined solid oxide electrolyte and calcining the mixture. The method includes forming an electrode assembly, forming the SOFC assembly, and coupling the SOFC assembly to a cooling system.

Abstract: Highly mesoporous activated carbon products are disclosed with mesoporosities characterized by mesopore volumes of 0.7 to 1.0 cubic centimeters per gram or greater. Also disclosed are activated carbon products characterized by a Molasses Number of about 500 to 1000 or greater. Also disclosed are activated carbon products characterized by a Tannin Value of about 100 to 35 or less. The activated carbon products may be further characterized by total pore volumes of at least 0.85 cubic centimeters per gram and BET surface areas of at least about 800 square meters per gram. The activated carbon product may be derived from a renewable feedstock.

Abstract: This invention introduces a method of preparing a carbon-based sulfur-loading iron-containing adsorbent for mercury removal, which can solve the problems in the prior art that sulfur-rich heavy organic materials have low-value utilization and the elemental mercury in atmosphere is hard to be efficiently and economically removed by the existing mercury removal agents. A carbon-based sulfur-loading iron-containing adsorbent for mercury removal is prepared in this invention. The adsorbent with a porous structure is prepared in situ by performing steps such as chemical activation of sulfur-rich heavy organic materials that are rich in iron. The adsorbent prepared herein has good mercury removal performance in simulated coal-fired flue gas. This invention not only improves the utilization value of sulfur-rich heavy organic materials, but also prevents SOX pollution caused by the combustion of sulfur-rich heavy organic materials and controls mercury pollution in the coal-fired flue gas.

Abstract: Composition comprising a) a polymer comprising recurring units derived from vinylidene fluoride monomer and at least one monomer carrying at least one functional group selected from carboxyl groups, ester groups and hydroxyl groups, and b) a microporous adsorbent carbon material having a specific surface area (BET) of at least 700 m2/g, a pore volume in the range of from 0.1 to 0.7 m3/g, at least 60% of said pore volume being formed by micropores having a pore radius of 2 nm or less.

Abstract: An object of the present invention is to provide a method for removing geniposide or genipin or both from a material containing geniposide or genipin or both. The present invention is a method for removing geniposide or genipin or both from a material containing geniposide or genipin or both, the method comprising treating the material containing geniposide or genipin or both using an activated carbon having (a) a methylene blue adsorption ability of 50 ml/g or more; and (b) an iodine adsorption ability of 750 mg/g or more, thereby removing geniposide or genipin or both.

Abstract: In one aspect, the disclosure relates to processes for preparation of a carbon foam material, the process comprising heating in a microwave heating apparatus a mixture comprising a coal material and a flux agent. In other aspects, relates to processes for preparation of a carbon foam material, the process comprising heating in a microwave heating apparatus a mixture comprising a coal material, a foaming pitch material and a flux agent. In a further aspect, the mixture comprising a coal material, a foaming pitch material and a flux agent after heating in the microwave heating apparatus can form a pseudo-fluid material. In a still further aspect, the pseudo-fluid material can be arranged in mold, and then further heated to form a carbon foam. The disclosure, in further aspects, relates to processes further providing carbon materials such as carbon composite materials, graphite, graphite flakes, and graphene.

Abstract: The present invention provides a composite conductive material having excellent dispersibility and a method for producing the same. In an embodiment, the method includes supporting a catalyst on surfaces of carbon particles; heat treating the catalyst in a helium or hydrogen atmosphere such that the catalyst penetrate the surfaces of the carbon particles and are impregnated beneath the surfaces of the carbon particles at a contact point between the carbon particles and the impregnated catalyst; and heating the carbon particles having the impregnated catalyst disposed therein in the presence of a source gas to grow carbon nanofibers from the impregnated catalyst to form a composite conductive material, wherein the source gas contains a carbon source, and wherein the carbon nanofibers extend from the contact point to above the surfaces of the carbon particles.

Abstract: The present disclosure provides composites comprising an open cell foam and a small pore area material, methods for their preparation, articles of manufacture comprising them and methods for preparing the same.

Abstract: Provided herein is a method for manufacturing activated carbon that providing a carbon material in a reactor, carbonizing the carbon material by a first heat-treating under an inert gas atmosphere, first activating the carbonized carbon material by a second heat-treating under an oxidizing gas atmosphere, and second activating the first activated material by a third heat-treating under a carbon dioxide atmosphere.

Abstract: The present application is directed to methods for solvent-free preparation of polymers and their subsequent processing into activated carbon materials. These methods unexpectedly demonstrate ability to tune pore structure in the polymer gel and carbon produced there from, while also providing distinct advantages over the current art.

Abstract: A carbonaceous material, based on the total weight of the carbonaceous material, contains 1-99 wt % of a carbon element, 0.2-60 wt % of a magnesium element, 0.5-60 wt % of an oxygen element and 0.1-40 wt % of a chlorine element. The process for preparing the carbonaceous material include (1) Mixing a solid carbon source, a precursor and water to produce a mixture; wherein said precursor contains a magnesium source and a chlorine source; (2) Drying the resulting mixture obtained in Step (1) to produce a dried mixture; and (3) Calcining the dried mixture obtained in Step (2). The carbonaceous material can be used in catalytic oxidation of hydrocarbons.

Abstract: The invention concerns high-performance adsorbents based on activated carbon of high meso- and macroporosity which are present in the form of discrete grains of activated carbon, wherein: at least 55% of the total pore volume of the high-performance adsorbents are formed by pores (i.e. meso- and macropores) having pore diameters of more than 20 ?, the high-performance adsorbents have a measure of central tendency pore diameter of more than 25 ?, and the high-performance adsorbents have a BET surface area of at least 1250 m2/g. These high-performance adsorbents are obtainable by a novel process comprising specific two-stage activation, and have, in addition to the aforementioned properties, an excellent abrasion and bursting resistance, so that they are useful for a multiplicity of different applications.

Abstract: A carbon pyrolyzate material is disclosed, having utility as an adsorbent as well as for energy storage and other applications. The pyrolyzate material comprises microporous carbon derived from low cost naturally-occurring carbohydrate source material such as polysaccharides. In adsorbent applications, the carbon pyrolyzate may for example be produced in a particulate form or a monolithic form, having high density and high pore volume to maximize gas storage and delivery, with the pore size distribution of the carbon pyrolyzate adsorbent being tunable via activation conditions to optimize storage capacity and delivery for specific gases of interest.

Abstract: An energy storage device such as an electric double layer capacitor has positive and negative electrodes, each including a blend of respective first and second activated carbon materials having distinct pore size distributions. The blend (mixture) of first and second activated carbon materials may be equal in each electrode.

Abstract: A process for treating a composition comprising one or more desired (hydro)halocarbons and one or more undesired halogenated hydrocarbon containing impurities so as to reduce the concentration of at least one undesired halogenated hydrocarbon containing impurity, the process comprising contacting the composition with an adsorbent comprising a carbon molecular sieve.

Abstract: A method for using plasma to activate biochar is disclosed where reactive gas(es) are excited by external power; biochar set on a sample holder is electrically biased or set at a floating potential so that charged particles of a certain type are attracted to the biochar, leading to intensive chemical reactions.

Abstract: A pyrolyzed monolith carbon physical adsorbent that is characterized by at least one of the following characteristics: (a) a fill density measured for arsine gas at 25° C. and pressure of 650 torr that is greater than 400 grams arsine per liter of adsorbent; (b) at least 30% of overall porosity of the adsorbent including slit-shaped pores having a size in a range of from about 0.3 to about 0.72 nanometer, and at least 20% of the overall porosity including micropores of diameter <2 nanometers; and (c) having a bulk density of from about 0.80 to about 2.0 grams per cubic centimeter, preferably from 0.9 to 2.0 grams per cubic centimeter.

Abstract: To reduce size and weight of canister while improving adsorbing/desorbing performance by optimizing adsorbent that fills chamber located at air release side. Adsorbent filling chambers 8, 9 located at air port 5 side, of a plurality of chambers 5˜8 that are arranged in series along an air flow direction in case 2, is formed by macroscopic pore whose diameter is 50 nm or greater. The adsorbent has hollow cylindrical shape whose inside thickness is 0.6 to 1.5 mm and whose outside diameter is 4 to 6 mm or hollow spherical shape whose inside thickness is 0.6 to 1.5 mm and whose diameter is 4 to 6 mm. A ratio of volume of the macroscopic pore whose diameter is less than 500 nm to total volume of the macroscopic pore whose diameter is equal to or greater than 50 nm is within a range of 30 to 70%.

Abstract: The invention relates to: a pre-treatment method for plant biomass hydrolysis reaction raw materials characterized in comprising a process for mixing a solid catalyst and solid substrate beforehand and grinding same simultaneously (grinding process); a plant biomass hydrolysis reaction raw material pre-treated by said pre-treatment method; and a plant biomass saccharification method comprising a process for hydrolyzing said hydrolysis reaction raw material. The invention provides an efficient and practical pre-treatment method for plant biomass hydrolysis reaction raw materials that can improve the saccharification yield and saccharide concentration of plant biomass hydrolysis reactions, a plant biomass hydrolysis reaction raw material obtained therefrom, and a plant biomass saccharification method.

Abstract: A composition is provided that includes mesoporous starburst carbon domains. Each of the mesoporous starburst carbon domains is incorporated with particles of metal or metal oxide in an amount of from 40 to 85 total weight percent of the composition. The metal or metal oxide particles can include tin, cobalt, copper, molybdenum, nickel, iron, or ruthenium, or an oxide thereof. The resulting composition when combined with a binder forms a battery electrode. Such a battery electrode operating as an anode in a lithium ion battery has gravimetric capacity of more than 1000 milliampere hours per gram after 15 galvanostatic cycles.

Abstract: A method of producing an activated carbon, comprising selecting a raw material for direct-activation, applying a solution of at least 50% phosphoric acid by weight at a ratio of from 0.01 pounds to 0.3 pounds of phosphoric acid solution per pound to the raw material selected for direct activation to produce a phosphoric acid treated raw material, and direct-activating the phosphoric acid treated raw material via a gas activation process to produce an activated carbon.

Abstract: A method of forming a structured adsorbent sheet is provided. The method includes, combining a nano-adsorbent powder and a binder material to form an adsorbent material, and sandwiching a porous electrical heating substrate between two layers of adsorbent material. The nano-adsorbent powder may be a nano-particle adsorbent. The nano-adsorbent powder may be selected from the group consisting of crystal zeolite, activated carbon, activated alumina, silica gel, and metal organic framework (MOF).

Abstract: Provided are an adsorptive carbon which can effectively adsorb vivotoxins such as advanced glycation end products (AGEs), and an adsorbent containing the adsorptive carbon as an active ingredient. The adsorptive carbon according to the present invention has a total pore volume of 0.10 to 1.0 mL/g, an average pore diameter of 1.0 to 2.0 nm, and an absorbance of an infrared absorption band at 1650-1800 cm?1 of no less than 0.005.

Abstract: Biomass combustion processes may be controlled to intentionally generate a carbon-containing ash, from which activated carbon is produced according to the methods disclosed. Some variations provide an economically attractive process for producing an activated carbon product, the process comprising combusting a carbon-containing feedstock to generate energy, combustion products, and ash, wherein the ash contains at least 10 wt % carbon; separating and recovering carbon contained in said ash; and further activating or treating the separated carbon, to generate an activated carbon product. Many process variations are disclosed, and uses for the activated carbon product are disclosed.

Abstract: A carbon adsorbent adapted for adsorptive storage and subsequent desorptive release of a decomposition-susceptible gas is described. Such carbon adsorbent comprises porosity in which mesopore volume is less than 0.25 cm3/gm of carbon adsorbent, in which the porosity comprises at least 80% by volume micropores, and at least 65% by volume of the micropores have pore diameter in a range of from 0.3 to 0.72 nm. The carbon adsorbent has a nitrogen adsorption BET surface area greater than 800 m2/g of carbon adsorbent, measured at 77° K, and a bulk density that is greater than 0.55 g/cc of carbon adsorbent. The carbon adsorbent can be utilized in gas storage and dispensing packages of varying type, to provide a safe and reliable source of decomposition-susceptible gas, e.g., acetylene for applications such as gas welding/cutting applications, atomic absorption spectroscopy applications, chemical synthesis and microelectronic products manufacturing.

Abstract: An adsorbent media has a pore volume/media volume of at least about 0.12 cc pore volume/cc media, a specific heat capacity of less than about 2.9 J/cc pore volume, and a pressure drop of less than about 4.0 inH2O/ft media at a superficial air velocity of about 500 ft/min, wherein the adsorbent media is in a concentrator system. An extruded honeycomb adsorbent media has a cell density of more than about 200 cells per square inch (cspi), % open area of at least about 50%, an activated carbon content of at least about 50% by weight based on total weight, and a pressure drop of less than about 4.0 inH2O/ft media at a superficial fluid velocity of about 500 ft/min.

Abstract: Nanoporous activated carbon material having a high specific capacitance in EDLCs and controlled oxygen content, and methods for making such activated carbon material. Reduction of oxygen content is achieved by (a) curing a carbon precursor/additive mixture in an inert or reducing environment, and/or (b) refining (heating) activated carbon material after synthesis in an inert or reducing environment. The inert or reducing environment used for curing or refining is preferably substantially free of oxygen.

Abstract: In at least one embodiment, a compressed gaseous fuel storage pellet is provided comprising a gas adsorbent material and a thermally conductive material extending substantially an entire dimension of the pellet and having a thermal conductivity of at least 75 W/mK. The pellet may include at least two layers of gas adsorbent material spaced apart along a compression direction of the pellet and a substantially continuous layer of the thermally conductive material disposed between the at least two layers of gas adsorbent material. The pellet may further include thermally conductive projections which intersect the layer(s) of thermally conductive material.

Abstract: Catalyst compositions comprising molybdenum, sulfur and an alkali metal ion supported on a nanofibrous, mesoporous carbon molecular sieve are useful for converting syngas to higher alcohols. The compositions are produced via impregnation and may enhance selectivity to ethanol in particular.

Abstract: An absorbent pad that contains activated carbon to reduce confinement odor in a vacuum-packaged food product is provided. An embodiment of absorbent pad contains activated carbon and an antimicrobial agent that further reduces confinement odor by two mechanisms of action: reducing bacterial counts in the liquid purge that cause breakdown of carbohydrates and proteins in food products; and trapping of confinement odor-causing breakdown products by the activated carbon. The absorbent body in the absorbent pad actively draws in liquid purge and dissolved volatile breakdown products in the vacuum package that produce confinement odor, which produces greater and more rapid contact of odor-causing compounds with the activated carbon.

Abstract: The invention provides a hydrogen storage material comprising a porous carbon material having oxygen-containing functional groups on the surface, and Li bonded to the surface of the porous carbon material. The hydrogen storage material of the invention has more excellent hydrogen storage capacity than the prior art.

Abstract: There is provided a method for producing a graphite material and a graphite material produced by the method The method includes a kneading step of adding a hydrophobic binding material to a first carbonaceous raw material containing coke powder, followed by heat kneading to obtain a mixture, a pulverizing step of pulverizing the mixture obtained in the kneading step to obtain a second carbonaceous raw material, a granulating step of obtaining a granulated powder using the second carbonaceous raw material obtained in the pulverizing step, a hydrophilic binding material and a solvent, a molding step of subjecting the granulated powder obtained in the granulating step to cold isostatic press molding to obtain a molded body, a burning step of burning the molded body obtained in the molding step to obtain a burnt product, and a graphitizing step of graphitizing the burnt product obtained in the burning step.

Abstract: Provided is a composite adsorbent material and a method for preparing the same. The composite adsorbent material comprises a porous host material of activated carbon impregnated with silica-gel and calcium chloride, and is useful for adsorbing high levels of water vapor. The composite adsorbent material is used in low temperature heat driven adsorption cooling and dehumidification systems.

Abstract: A system for converting solar energy to chemical energy, and, subsequently, to thermal energy includes a light-harvesting station, a storage station, and a thermal energy release station. The system may include additional stations for converting the released thermal energy to other energy forms, e.g., to electrical energy and mechanical work. At the light-harvesting station, a photochemically active first organometallic compound, e.g., a fulvalenyl diruthenium complex, is exposed to light and is photochemically converted to a second, higher-energy organometallic compound, which is then transported to a storage station. At the storage station, the high-energy organometallic compound is stored for a desired time and/or is transported to a desired location for thermal energy release.

Abstract: Mesoporous activated carbon is disclosed. In at least some embodiments, virgin activated carbon to be processed may be coconut shell-based. The enhanced activated carbon may have a mesopore structure of at least about 10%. The enhanced activated carbon may be produced through a calcium-catalyzed activation process. A chelator may also be used. Catalyzed thermal activation may be carried out until a desired mass loss is achieved.

Abstract: A method produces activated carbon, suitable in particular for use in double-layer condensers. The method includes a) producing a mixture of a preferably pulverulent carbon material, a base and a hydrophilic polymer chemically inert to the base, b) pressing the mixture produced in step a) to form a pressing and c) activating the pressed body produced in step b).

Abstract: An adsorbent for an oral administration, comprising a surface-modified spherical activated carbon wherein an average diameter is 0.01 to 1 mm, a specific surface area determined by a BET method is 700 m2/g or more, a volume of pores having a pore diameter of 7.5 to 15000 nm is from 0.25 mL/g to 1.0 mL/g, a total amount of acidic groups is 0.30 to 1.20 meq/g, and a total amount of basic groups is 0.20 to 0.7 meq/g, is disclosed.

Abstract: Disclosed is a self-supporting solid compacted composition of material comprising an ammonia storage material capable of reversibly absorbing and desorbing ammonia in its ammonia saturated state and compacted to such a density that it has of at least 70% of the single crystal density of said material in its ammonia-saturated state in admixture with one or more additive incapable of storing ammonia and having a thermal conductivity of at least five times the thermal conductivity of the ammonia storage material at a temperature of from at least ?45° C. to 250° C., as well as a process for preparing it.

Abstract: Systems and methods for treating a fluid with a body are disclosed. Various aspects involve treating a fluid with a porous body. In select embodiments, a body comprises ash particles, and the ash particles used to form the body may be selected based on their providing one or more desired properties for a given treatment. Various bodies provide for the reaction and/or removal of a substance in a fluid, often using a porous body comprised of ash particles. Computer-operable methods for matching a source material to an application are disclosed. Certain aspects feature a porous body comprised of ash particles, the ash particles have a particle size distribution and interparticle connectivity that creates a plurality of pores having a pore size distribution and pore connectivity, and the pore size distribution and pore connectivity are such that a first fluid may substantially penetrate the pores.

Abstract: Sorbents for removal of mercury and other pollutants from gas streams, such as a flue gas stream from coal-fired utility plants, and methods for their manufacture and use are disclosed. Embodiments include brominated sorbent substrate particles having a carbon content of less than about 10%. Other embodiments include one or more oxidatively active halides of a nonoxidative metal dispersed on sorbent substrate particles mixed with activated carbon in an amount up to 30% by weight.

Abstract: A device for stabilizing fuel in a fuel tank comprises activated carbon. The activated carbon is configured to be inserted into or installed inside a fuel tank, so that it is in contact with the fuel. The device allows the activated carbon to be in contact with the fuel, but does not allow it to be dispersed in the fuel. A method for stabilizing fuel in a fuel tank comprises adding the device to the fuel tank so that it is in contact with the fuel.

Abstract: A hydrogen storage alloy unit comprises a porous body 7 having a large number of holes (spaces) 9 allowing hydrogen atoms to pass through, and a hydrogen storage alloy covering a surface of the porous body 7, inclusive of surfaces of the holes thereof. The hydrogen storage alloy includes a hydrogen storage base formed of a hydrogen storage material, and a catalytic layer covering a surface of the hydrogen storage base. The porous body 7 is formed of an assembly of hydrogen storage fibers 8 formed by vapor-depositing the hydrogen storage alloy onto nanofibers.

Abstract: A carbon or ceramic monolithic materials with an M2 (macroporous/microporous) hierarchised porous structure is provided as well as method for preparing said materials using a macro/meso/microporous silica cavity. Such materials may be used, in particular for the production of hydrogen purifiers, supercapacitors or electrodes, or else for carrying out catalysed chemical reactions in a heterogeneous phase.

Abstract: An orally administered adsorbent which has a high ability of adsorbing indoxylsulfuric acid, indoleacetic acid, and indole, a method permitting easy and advantageous production of the same, and a drug using the same. The orally administered adsorbent is obtained from spherical particles of activated carbon by carbonizing and activating spherical particles of a furfuryl alcohol resin obtained by resinifying furfuryl alcohol through a self-condensation reaction and curing the resinified furfuryl alcohol.

Abstract: An active material of the present invention has fine pores formed in the interlayer of a carbon material capable of exhibiting electrochemical double layer capacitance. The fine pores are formed by forming an oxidized graphite structure combined with oxygen in the interlayer of a part or whole of the carbon material containing soft carbon and then removing a part or whole of oxygen in the interlayer. A method for producing an energy storage active material for use in an electrochemical double layer capacitor comprises pre-treating a carbon material through heat treatment and oxidizing the pre-treated carbon material using an oxidant. The method further comprises reducing the oxidized carbon material through heat treatment. The interlayer distances of an active material for respective steps, measured by a powder X-ray diffraction method, are 0.33˜0.36 nm in the pre-treatment step, 0.5˜2.1 nm in the oxidation step, and 0.34˜0.5 nm in the reduction step.

Abstract: Adsorbed natural gas (ANG) technology is an energy efficient approach for storing NG at room temperature and low pressure. ANG technology can be applied to several aspects of the NG industry. The usage of an adsorbent material in natural gas storage and transport may provide increased storage density of NG at a given pressure and decreased pressure of gaseous fuel at a given gas density. Such adsorbent materials have been shown to store substantial quantities of natural gas at relatively modest pressures. Because lower-pressure vessels can be far less expensive than comparable sized high-pressure vessels, ANG based storage can be used to lower the cost of storing natural gas in various applications.

Abstract: The present invention involves the use of nanoporous carbons derived from partially or fully demetalized metal carbides in personal protection equipment for the irreversible absorption/adsorption of both broad and specific targeted gases. These materials have been specifically processed to provide enhanced effective loadings against specific harmful volatile organic compounds.

Abstract: The present invention provides for a device for reducing a volatile organic compound (VOC) content of a gas comprising a manganese oxide (MnOx) catalyst. The manganese oxide (MnOx) catalyst is capable of catalyzing formaldehyde at room temperature, with complete conversion, to CO2 and water vapor. The manganese oxide (MnOx) catalyst itself is not consumed by the reaction of formaldehyde into CO2 and water vapor. The present invention also provides for a device for reducing or removing a particle, a VOC and/or ozone from a gas comprising an activated carbon filter (ACF) on a media that is capable of being periodically regenerated.

Abstract: A method of producing an activated carbon, comprising selecting a raw material for direct-activation, applying a solution of at least 50% phosphoric acid by weight at a ratio of from 0.01 pounds to 0.3 pounds of phosphoric acid solution per pound to the raw material selected for direct activation to produce a phosphoric acid treated raw material, and direct-activating the phosphoric acid treated raw material via a gas activation process to produce an activated carbon.

Abstract: A method for producing an activated carbon material includes forming an aqueous mixture of a natural, non-lignocellulosic carbon precursor and an inorganic compound, heating the mixture in an inert or reducing atmosphere, cooling the heated mixture to form a first carbon material, and removing the inorganic compound to produce an activated carbon material. The activated carbon material is suitable to form improved carbon-based electrodes for use in high energy density devices.