Abstract: A reduced puffing needle coke is formed, which includes a reduced nitrogen content within the coke so that the coke particles do not experience as much puffing during the formation of graphitized carbon articles produced from such coke upon heating to graphitization temperatures.

Abstract: The invention concerns materials for eliminating oxides of nitrogen NO and NO2 present in exhaust gases, in particular from the internal combustion engines of automotive vehicles operating in a medium which is super-stoichiometric in oxidising agents, which can adsorb oxides of nitrogen then desorb the oxides of nitrogen by elevating the temperature with respect to the adsorption temperature or by passage of a rich mixture, said materials comprising mixed oxides the metals of which are in octahedral coordination, with the octahedra connecting together so that the structure generates lamellae. Said materials adsorb oxides of nitrogen by insertion and do not become poisoned in contact with oxides of sulphur and carbon contained in the gases. In the presence of a group VIII metal, said materials are capable of eliminating oxides of nitrogen adsorbed by reduction during the passage of a rich mixture.

Abstract: Mats for absorbing one or more fluids are disclosed. The mats comprise fiberglass and optionally, one or more additional fibers, such as low melt thermoplastic binders. Multilayer are disclosed featuring glass fiber sandwiched between one or more nonwoven fabrics on one or more faces. Methods for manufacturing and using the mats to absorb/adsorb one or more fluids are disclosed. A medium comprising fiberglass and one or more sources of additional fiber is also disclosed, as are kits for absorbing fluids using the mats or the medium.

Abstract: Provided herein are adsorbents and methods of using the adsorbents to at least partially remove one or more adsorbates. In an aspect, an adsorbate within a phase is at least partially removed by providing an adsorbent material and contacting the adsorbent material with the phase having an adsorbate, to at least partially remove the adsorbate. Various adsorbents are disclosed having the chemical formula RE1-x-y-zBxB?yB?zOw, where RE is RE is a rare earth metal, B is a trivalent metal ion, B? is a transition metal ion or an alkaline earth element, B? is a transition metal ion, 0?x?0.25, 0?y?0.95, 0?z?0.75, w is a number which results in charge balance, and x+y+z<1.

Abstract: The invention relates to an adsorber element and to a method for the production thereof, comprising a carrier material (1) on which adsorbent particles (3) are arranged as the adsorber layer using a binding agent (2). According to the invention, the adsorber layer comprises inorganic fibers (4) and the binding agent (2) is designed as a colloid.

Abstract: An object of the present invention is to improve hydrocarbon adsorbing property when zeolite is used as an adsorbent for hydrocarbons. The present invention provides an adsorbent for hydrocarbons characterized by comprising A Type of ?-zeolite having a SiO2/Al2O3 ratio (molar ratio) in a range of 10 or more and less than 200 and B Type of ?-zeolite having a SiO2/Al2O3 ratio (molar ratio) in a range from 200 to 1,000, and a catalyst for exhaust gas purification containing said adsorbent for hydrocarbons.

Abstract: An object of the present invention is to provide an aqueous-liquid-absorbing agent which comprises water-absorbent resin particles as essential components and is suitable for uses in sanitary materials. As a means of achieving this object, an aqueous-liquid-absorbing agent according to the present invention is an aqueous-liquid-absorbing agent comprising water-absorbent resin particles as essential components, wherein the water-absorbent resin particles are obtained by a process including the step of polymerizing a water-soluble ethylenically unsaturated monomer and have a crosslinked structure in their inside; with the aqueous-liquid-absorbing agent exhibiting an absorption rate (FSR) of not less than 0.2 g/g/s, a water absorption capacity (CRC) of 5 to 25 g/g, a saline flow conductivity (SFC) of not less than 400×10?7 cm3·s/g, and a wet porosity of not less than 20%.

Abstract: A granular material having a high strength and a large BET specific surface area composed of porous particles comprising calcium oxide and calcium hydroxide wherein the calcium oxide is contained in an amount of 30 to 80 weight % based on a total amount of the calcium oxide and calcium hydroxide and the porous particles have a BET specific surface area of 40 m2/g or more, or composed of porous particles comprising calcium oxide, magnesium oxide, calcium hydroxide, and magnesium hydroxide wherein a ratio of an amount of magnesium to a total of an amount of calcium and an amount of magnesium is in the range of 0.05 to 0.80, a total hydroxide content in the whole particles is in the range of 1 to 20 weight % and the porous particles have a BET specific surface area of 50 m2/g or more.

Abstract: Compositions, and processes utilizing such compositions, are provided for reducing mercury emissions during fuel combustion Such compositions comprise a sorbent, a bromine source and a chlorine source Such compositions exhibit improved thermal stability as compared to that of the sorbent by itself.

Abstract: A system for reversibly storing hydrogen includes a storage tank with an internal volume with a thermally conducting composite material situated within the storage tank and having a three-dimensional and interconnected framework of a conductive metal within the internal volume of the storage tank.

Abstract: The present invention provides a method for constructing a fractal network structure in hydrogen storage material to improve the hydrogen uptake at room temperature, the method including the following steps: providing a hydrogen storage material comprising a source and a receptor of hydrogen atoms, wherein the source is disposed above the receptor, and a chemical bridge is disposed between the source and the receptor, wherein the chemical bridge is composed of precursor material; and treating the hydrogen storage material to construct a fractal network structure of mesopores and micropores in the receptor, so as to enhance the hydrogen storage capacity of the hydrogen storage material at room temperature.

Abstract: This invention relates to novel adsorbent compositions for adsorbing pesticides like chlorpyrifos and malathion. This composition consists of nanoparticles of gold/silver supported on activated alumina or magnesia in powder or other forms. This invention includes a device and a method for decontaminating water contaminated with pesticides. This device consists of a housing provided with an inlet and an outlet. The housing is loaded with nanoparticles of gold/silver supported on activated magnesia. Contaminated water is allowed to pass through the housing while pesticides are adsorbed by the composition. Decontaminated water flows out through the outlet.

Abstract: Disclosed herein is an improved pan agglomeration process for forming porous absorbent particles suitable for use as an animal litter. The process eliminates the need for a pre-wetting step, while forming agglomerates that are up to 65% lighter in weight than the raw material feed. In addition, the agglomerates can incorporate performance-enhancing actives, such as odor-controlling carbon.

Abstract: In one embodiment, a hydrogen storage system includes a core of hydrogen sorbent material and a shell of crystalline metal hydride material enclosing at least a portion of the core of hydrogen sorbent material. In another embodiment, the hydrogen storage system further includes an intermediate layer of amorphous metal hydride material, at least a portion of which being positioned between the core of hydrogen sorbent material and the shell of crystalline metal hydride material.

Abstract: According to one aspect of the present invention, a hybrid hydrogen storage system is provided. In one embodiment, the hybrid hydrogen storage system includes: a first hydrogen storage material present at a first volume percent (%) having a first gravimetric capacity and a first volumetric capacity; and a second hydrogen storage material forming an unreacted mixture with the first hydrogen storage material and present at a second volume % being 100 volume % minus the first volume %, the second storage material having a second gravimetric capacity and a second volumetric capacity, the first gravimetric capacity at the first volume % being higher or lower than the second gravimetric capacity at the second volume %, and the first volumetric capacity at the first volume % being the other of higher or lower than the second volumetric capacity at the second volume %.

Abstract: Sorbent components containing calcium, alumina, and silica are used in combination during coal combustion to produce environmental benefits. Sorbents are added to the coal ahead of combustion and/or are added into the flame or downstream of the flame, preferably at minimum temperatures to assure complete formation of the refractory structures that result in various advantages of the methods. When used together, the components reduce emissions of elemental and oxidized mercury; increase the level of Hg, As, Pb, and/or Cl in the coal ash; decrease the levels of leachable heavy metals (such as Hg) in the ash, preferably to levels below the detectable limits; and make a highly cementitious ash product.

Abstract: A method for preparing radioactive-substance adsorbent depositing on a carriable structure is revealed. The method uses a supercritical fluid to mix a first solution with a carrier. The first solution includes an extractant dissolved in a first solvent. By low surface tension and high permeability of the supercritical fluid, the extractant in the first solution deposit evenly on the carrier so as to form an adsorbent. Thus the adsorbent formed provides better adsorptivity for the radioactive substances.

Abstract: Novel uses and methods of use for inorganic and macroreticulate polymer bonding to metals to control moisture and oxygen in OLED, and other like devices, are provided. Materials having color change capacity are also provided for the removal of moisture from an OLED, where the material changes color upon reaching its capacity and thereby signals the user that the OLED is no longer protected from moisture damage.

Abstract: Discloses are stabilized calcium pyrophosphate nanotubes, a process for making calcium pyrophosphate nanotubes comprising agitating at less than 2 OkHz an aqueous suspension of a calcium and a phosphate for a time sufficient to precipitate said inorganic calcium pyrophosphate nanotubes, and uses thereof.

Abstract: A composite sorbent material is disclosed which comprises A) a housing of a dense, insoluble material having openings therein and B) a porous polymer gel housed within said housing, said housing being provided with openings therein for fluid communication between said porous monolithic polymer gel and the surroundings, and said porous monolithic polymer gel occupying the inner space of said housing and being kept on place within said housing by mechanical means. Processes for the preparation of composite sorbent materials by cryoprecipitation are also disclosed as well as the use of the composite sorbent material according to the invention e.g. for the removal of pollutants from gases or liquids, for the enrichment or separation of molecules and for cell culture.

Abstract: Disclosed are a liquid heating element and a method for production thereof, and more particularly a solid ingredient A, a liquid ingredient B produced from the solid ingredient A, a liquid heating element produced from the liquid ingredient B and a method for producing the liquid heating element. The solid ingredient is produced by heating activated carbon, kaolin, copper sulfide and phosphoric acid (H3PO4) to a temperature ranging from 1,000 to 1,200° C. The liquid ingredient H is produced by mixing the solid ingredient A with silicon powder and distilled water and heating the mixture. The liquid heating element is produced by mixing the liquid ingredient B with ethylene glycol, leaving the mixture and then filtering the mixture. Since the liquid heating element is very stable and generates heat with minimum power consumption, it can be applied to various heat management systems.

Abstract: Compositions and associated methods directed to the removal of sulfurous compounds from air are presented herein. The compositions and methods may be able to treat air with H2S concentrations of at least 1000 ppm. The compositions and associated methods are used to remove sulfurous compounds from air associated with wastewater systems in various aspects.

Abstract: The present invention relates to a catalyst for reducing mercury, which comprises a reagent comprising any of the sulfites of potassium, sodium, calcium and magnesium, or any of the phosphates thereof, or a combination of them, as a main reagent of a catalyst component. And the present invention relates to the catalyst for reducing mercury, wherein the catalyst component is mixed with a different salt as an agent for inhibiting crystallization of the catalyst component.

Abstract: An adsorbent including a porous member having holes and a nanostructure formed on at least a portion of a surface of the porous member, and an air cleaning device including the adsorbent. A porous filter including a porous member having holes and a nanostructure formed on at least a portion of a surface of the porous member, and an air cleaning device including the porous filter. A method of cleaning air for decomposing a hazardous substance using the porous filter and a decomposition gas including a superheated water vapor. A method of manufacturing a porous filter including the steps of growing a nanostructure on at least a portion of a surface of a porous member having holes, allowing a catalyst particle to be contained in a dispersion gas including a superheated water vapor, and spraying the dispersion gas on a surface of the nanostructure to attach the catalyst particle thereto.

Abstract: A deoxidizer includes a porous body of fluorite-type cerium oxide represented by CeOx (where x is a positive number smaller than 2) and having a reversible oxygen deficiency. The deoxidizer has a specific surface area of 0.6 to 1.8 m2/g and a pore median diameter of 1.6 to 5.3 ?m. The cerium oxide used for the deoxidizer is produced by: firing a cerium-containing salt in the atmosphere at 500° C. to 1400° C. for 1 to 20 hours, to produce fluorite-type cerium oxide composed of a porous body; and firing the cerium oxide at 700° C. to 1100° C. for 1 to 3 hours in a reducing atmosphere having a hydrogen concentration equal to or above the lower explosive limit, to remove oxygen from the cerium oxide and produce the fluorite-type cerium oxide represented by CeOx and having a reversible oxygen deficiency.

Abstract: The present invention pertains to a natural product litter composition as well as methods of preparing and using a natural product litter as a sorbent for liquids. The sorbent contains 1 to 10% by weight Aspen particles and 90 to 99% by weight ground grain byproducts including red dog wheat and wheat middlings. The sorbency of a ground grain litter can be improved by pelletization and crumbling.

Abstract: The present invention relates to a method for the production of a quickly wettable material containing natural hydrocolloid in the form of a shaped body, in which a material containing natural hydrocolloid in the form of a shaped body is exposed to a plasma.

Abstract: In one aspect, the invention provides a hydrogen storage material that is formed by reacting solid precursors (a) and (b). The (a) precursor is a compound containing X—H and Y—H bonds, where X is a Group 13 and Y is a Group 15 element. Preferably X is boron (B—H) and Y is nitrogen (N—H). Most preferably, the precursor (a) is borazane. The (b) precursor is preferably a hydride, such as LiH or LiAlH4. Another feature of the present invention is a novel hydrogen storage composition material that is formed as an intermediate (INT) in the reaction of the (a) with the (b) precursors. The INT hydrogen storage material can be a quaternary B—H—Li—N composition. Other aspects of hydrogen storage materials are provided herein.

Abstract: The present invention relates to a method for isolating and/or purifying at least one polypeptide from a polypeptide-containing sample, characterized in that the sample is contacted with a boron carbide support material at a pH which allows the binding of the polypeptide to the boron carbide support material. Such isolating can, for example, be used to remove polypeptides from a sample or else to purify and/or to concentrate polypeptides. A matrix comprising a boron carbide support material for purification of polypeptides is further disclosed according to the invention.

Abstract: A fuel cell system includes: a fuel supply unit supplying a fuel; an air supply unit supplying air; a stack including a membrane electrode assembly (MEA) having an air path and a fuel path; a gas-liquid separator connected to an outlet of the fuel path and an outlet of the air path for separating gas-liquid into high-temperature liquid and moisture gas; a mixer mixing the high-temperature liquid separated by the gas-liquid separator and a fuel supplied from the fuel supply unit and connecting the gas-liquid separator and the MEA; a moisture absorbent connected to the gas-liquid separator to absorb condensed liquid in the high-temperature moisture gas; and a heat exchanger to vaporize the liquid absorbed by the moisture absorbent.

Abstract: Herein are disclosed adducts of amines and polycarboxylic acids, and methods of making such adducts. Such adducts can be used to remove cyanogen chloride. Also disclosed are methods of providing such adducts on supports to form filter media. Also disclosed are methods of combining such filter media with catalysts and/or with porous polymeric webs to form filter systems.

Abstract: Using zeolites as the active adsorbent, adsorbent laminates have been fabricated with various sheet supports. These adsorbent laminates have been successfully operated for oxygen enrichment at high PSA cycle frequencies, such as upwards of at least 150 cycles per minute. Methods for making suitable adsorbent laminates are described. The methods generally involve forming a slurry comprising a liquid suspending agent, an adsorbent and a binder. Laminates are made by applying the slurry to support material or admixing support material with the slurry. The slurry can be applied to support material using a variety of techniques, including roll coaters, split roll coaters, electrophoretic deposition, etc. One method for making laminates by mixing support material with the adsorbent slurry comprises depositing the slurry onto a foraminous wire, draining the slurry material, and pressing the material to form a ceramic adsorbent paper. Spacers can be formed on adsorbent laminates to space one laminate from another.

Abstract: An adsorption structure is described that includes at least one adsorbent member formed of an adsorbent material and at least one porous member provided in contact with a portion of the adsorbent member to allow gas to enter and exit the portion of the adsorbent member. Such adsorption structure is usefully employed in adsorbent-based refrigeration systems. A method also is described for producing an adsorbent material, in which a first polymeric material is provided having a first density and a second polymeric material is provided having a second density, in which the second polymeric material is in contact with the first polymeric material to form a structure. The structure is pyrolyzed to form a porous adsorbent material including a first region corresponding to the first polymeric material and a second region corresponding to the second polymeric material, in which at least one of the pore sizes and the pore distribution differs between the first region and the second region.

Abstract: The present invention is a method and material for using a sorbent material to capture and stabilize mercury. The method for using sorbent material to capture and stabilize mercury contains the following steps. First, the sorbent material is provided. The sorbent material, in one embodiment, is nano-particles. In a preferred embodiment, the nano-particles are unstabilized nano-Se. Next, the sorbent material is exposed to mercury in an environment. As a result, the sorbent material captures and stabilizes mercury from the environment. In the preferred embodiment, the environment is an indoor space in which a fluorescent has broken.

Abstract: The present invention is a method and material for using a sorbent material to capture and stabilize mercury. The method for using sorbent material to capture and stabilize mercury contains the following steps. First, the sorbent material is provided. The sorbent material, in one embodiment, is nano-particles. In a preferred embodiment, the nano-particles are unstabilized nano-Se. Next, the sorbent material is exposed to mercury in an environment. As a result, the sorbent material captures and stabilizes mercury from the environment. In the preferred embodiment, the environment is an indoor space in which a fluorescent has broken.

Abstract: The present invention is within the field of chromatography. More precisely, it relates to a novel chromatography medium, namely a hydrophobic medium provided with different lids excluding molecules over a certain size due to the porosity of the hydrophobic medium and/or the porosity of the lid. The invention also relates to use of the separation medium for purification of large molecules, which do not enter the separation medium, as well as small molecules, which enter the separation medium and are eluted from there.

Abstract: The present invention relates to a doped hydrogen storage material according to the general formula: MgxByMzHn wherein: (i) the ratio of x/y is in the range of from 0.15 to 1.5; (ii) z is in the range of from 0.005 to 0.35; (iii) x+y+z equals 1; (iv) M= is one or more metals selected from the group of selected Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu and Zn; (v) n is no more than 4y; and wherein x/y does not equal 0.5 and at least part of the doped hydrogen storage material is amorphous. The present invention further relates to the use of doped hydrogen storage materials according to the invention for storing hydrogen and a method for reversibly desorbing and/or absorbing hydrogen.

Abstract: An absorbent includes a ferromagnetic nucleus with a one-layer or two-layer shell or devoid thereof and the nucleus is embodied in the form of a plate with a planar size that ranges from 500-5000 ?m and the thickness is equal to 0.1-1000 ?m. The method for producing the inventive magnetically-operated absorbent includes evaporating and/or melting a magnetic material powder in a low-temperature plasma, quenching and condensing the thus obtained vaporized and/or melt-particle product in a gas flux, and transferring the product precipitated in the form of crystals or micro slugs of corresponding metals, correspondingly to a stabilizer-containing dispersion medium and holding in the medium until a gas release is over. Then the crystals or micro slugs are processed by flattening, for example pressing so that the plates of a specified thickness are obtained.

Abstract: Disclosed are porous-shell particles, methods of making the particles, and uses thereof. In one aspect, the porous-shell particles are superficially porous particles.

Abstract: The invention relates to sorption materials for removing of heavy metal ions from ground water and surface aquifer systems, and can be used by enterprises in chemical and metallurgical industry which utilize etching and galvanic technologies. The sorbent for removing of heavy metal ions from water is composed of ground zeolite and nanophase material, where the nanophase material consists of nanophase iron hydroxide and nanophase boehmite in the following ratio, mass %: Nanophase iron hydroxide 12-18 Nanophase boehmite ?5-13 Ground zeolite the rest. Technical result is the enhanced purification effectiveness of the sorbent due to a wider range of heavy metals it can absorb when purifying highly contaminated water.

Abstract: Carbon monoxide is removed from streams by adsorption on an adsorption composition which comprises copper, zinc and zirconium oxides and whose copper-comprising component has a degree of reduction, expressed as weight ratio of metallic copper to the sum of metallic copper and copper oxides, calculated as CuO, of at least 45% and not more than 75%.

Abstract: Metal sorbent compositions for removing a metal contaminant from a fluid, such as removal of mercury from a coal-fired flue gas stream, and methods for making and using the same are provided. The subject metal sorbent compositions comprise an effective amount of an aqueous dispersion of microfine elemental sulfur particles on an adsorbent substrate, and optionally, a metal capture enhancing agent such as a halogen source and/or an oxidizing agent in an amount providing a metal capture enhancing effect on the metal sorbent composition. The subject metal sorbent compositions are prepared by drying an aqueous dispersion of microfine elemental sulfur particles on an adsorbent substrate, such as on a substrate of microfine particles of a refractory material and the like. Also provided are kits for use in preparing the subject compositions, and compositions produced by the methods. The subject compositions, kits and systems find use in a variety of different applications.

Abstract: The problem to be solved by the present invention is to provide a monolith adsorbent which can adsorb a target sample easily in a short time or regardless of whether the amount of the sample is small or large and extract the sample with a small amount of solvent, and easily secure the sample necessary for analysis, and a method and an apparatus for adsorption and retention using the same. The present invention, as the means for solving the problem, is a monolith adsorbent formed by allowing a monolith structure body to contain an adsorbing material such as activated carbon or graphite, exposing the adsorbing material on the surface of the structure body and further surface-treating the surface of the monolith structure body with a hydrophobic or hydrophilic compound or a resin.

Abstract: A method of making palladium-containing nanoscale catalyst particles comprising subjecting a starting material to laser energy so as to form a vapor and condensing the vapor so as to form the catalyst particles. The catalyst comprises nanoscale particles of palladium and/or palladium oxide incorporated in and/or on nanoscale particles of a metal or metal oxide. The nanoscale catalyst, which can be incorporated in the tobacco cut filler, cigarette wrapper and/or cigarette filter of a cigarette, is useful for low-temperature and near-ambient temperature catalysis. The nanoscale catalyst can convert carbon monoxide and nitric oxide that are found in mainstream smoke to carbon dioxide and nitrogen, respectively. The nanoscale catalyst may also be incorporated into a hydrocarbon conversion reactor, into a vehicle exhaust emissions system, into a laser, into a fuel cell or used in an air filter or for emissions reduction in the cold starting of an automobile engine.

Abstract: The present invention discloses a method and an apparatus for reactivating lime-based sorbents and increasing the carbon dioxide-capture capacity of the sorbent in the combustion of carbon-containing fuels. The method of the present invention seeks to increase the carbon dioxide capture capacity of lime-based sorbents by applying concentrated or 100% carbon dioxide directly to a lime-based sorbent. Optionally, the lime-based sorbent may be pretreated using a hydration process after each process of carbon dioxide separation. The regenerated sorbent is carbonated in a presence of concentrated carbon dioxide and elevated temperatures. The invention is useful in reducing the need to add additional sorbent to maintain the carbonation/calcination cycle. The regenerative potential of the sorbent as manifested by the present invention leads to increased carbon dioxide-capture capacity of the sorbent.

Abstract: The present invention provides a new molecular recognition material, wherein the control of morphology is possible and the selectivity and capture efficiency of the template molecule are excellent, and to provide a simple production method thereof. The molecular recognition material of the present invention is a core-shell particle, which has a shell layer on the core particle surface, and the material is characterized in that template molecules are imprinted on the above-described shell layer. And a production method of the molecular recognition material of the present invention comprising: (a) introducing an iniferter group on the core particle surface, (b) adsorbing the template molecule, after process (a), onto the core particle surface, and (c) forming the shell layer, after process (b), on the core particle surface.

Abstract: Provided are gas storage medium, a gas storage apparatus having the same and a method thereof. The gas storage medium includes a plurality of material layers each having a variable valence, wherein each of the material layers includes redundant electrons that are not participated in chemical bonding.

Abstract: A material compound comprising MgO. CaCO3 comprising granules of a size distribution between as a solid solution of MgO and CaCO3. and a method of fabricating the same.

Abstract: An agglomerate for use in economical bulk treatment of contaminated sediments with minimal environmental impact is formed from a sorbent, bentonite clay and sand. The agglomerate has sufficient density so as to sink through a water column into sediment below the water column and is still sufficiently light as to be capable of mixing with the sediment when subjected only to bioturbation. The agglomerate can be formed into pellets and applied to a water column over contaminated sediment by broadcast methods, so as to permit economical remediation of contaminated sediment with negligible environmental impact.

Abstract: Disclosed is a titanate nanostructure, especially, represented by a chemical formula of NaKTi3O7. A method for preparation of a titanate nanostructure is also provided. The method includes mixing titanium dioxide powder with an alkaline solution to prepare a titanium dioxide solution; and carrying out hydrothermal synthesis of the prepared titanium dioxide solution at a temperature of 120° C. to 180° C. for 12 to 72 hours.