Abstract: Boron nitride nanotubes are prepared by a process which includes: (a) creating a source of boron vapor; (b) mixing the boron vapor with nitrogen gas so that a mixture of boron vapor and nitrogen gas is present at a nucleation site, which is a surface, the nitrogen gas being provided at a pressure elevated above atmospheric, e.g., from greater than about 2 atmospheres up to about 250 atmospheres; and (c) harvesting boron nitride nanotubes, which are formed at the nucleation site.

Abstract: Sulfur dioxide (SO2) is removed from a carbon dioxide feed gas by maintaining the feed gas at elevated pressure(s) in the presence of oxygen (O2), water and NOx for a period of time sufficient to convert SO2 to sulfuric acid and NOx to nitric acid and produce SO2-depleted, NOx-lean carbon dioxide gas. The invention resides in separating the sulfuric and nitric acids from said SO2-depleted, NOx-lean carbon dioxide gas, and then neutralizing the acids by reaction with an alkaline sorbent in an acid/sorbent reactor system to produce sorbent-derive sulfate. The method has particular application in the removal of SO2 and NOx from flue gas produced by oxyfuel combustion of a carbonaceous fuel.

Abstract: Disclosed is a composition containing a fluorine-containing urethane compound (A) and a fluorine-containing polymer (B) having a repeating unit derived from a fluorine-containing monomer represented by the following formula (I): CH2?C(—X)—C(?O)-A-Rf??(I) (wherein X represents a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a CFX1X2 group (wherein X1 and X2 respectively represent a hydrogen atom, a fluorine atom or a chlorine atom), a cyano group, a straight or branched chain fluoroalkyl group having 1-20 carbon atoms, a substituted or unsubstituted benzyl group, or a substituted or unsubstituted phenyl group; A represents a divalent group; and Rf represents a straight or branched chain perfluoroalkyl group having 1-6 carbon atoms).

Abstract: A fuel cell is formed by stacking an electrolyte electrode assembly and a pair of separators alternately. Each of the separators includes first to third plates. A first cylindrical portion provided at a first small diameter end portion of one separator is inserted into a fuel gas supply passage of the other separator. The first cylindrical portion is subjected to a crimping process such that a joint portion as a predetermined overlapping portion is formed integrally with the one separator and the other separator.

Abstract: A method and system produce a synthesis gas from a biogas. The method provides a more economic process control and a higher yield. For this purpose hydrogen sulfide and carbon dioxide of the biogas are nearly completely separated in separate cleaning steps before a catalytic conversion of the biogas, wherein hydrogen sulfide is biologically removed by the admixture of oxygen and/or oxidation agents containing oxygen. The oxygen, or the oxidation agent, is dosed such that an excess of oxygen of at least 1.0 vol.-% is present in the cleaned biogas (methane gas). The biogas is concentrated without any dehumidification, heated, and mixed with superheated steam. Due to the excess of oxygen, thermal energy is additionally created during the reforming process by an exothermal oxidation of oxygen contained in the biogas together with hydrogen in the catalyst bed for the endothermal conversion of methane to the synthesis gas.

Abstract: The disclosure provides methods for preparation of multiphasic micro-components, such as core-shell or anisotropic (e.g., Janus) multiphasic particles with well-defined structures using electrohydrodynamic co-jetting of two polymer solutions containing polyelectrolytes. Suitable polyelectrolytes include polyacrylic acid (PAA), poly(acrylamide acrylic acid (PAAm), and/or poly(acryl amide-co-acrylic acid) (PAAm-AA), sodium polystyrene sulfonate (PSS), polyethylene imine (PEI), polypeptides, copolymers and combinations of these. Control of certain variables, such as relative conductivities of the two jetting solutions, controls the particle morphologies formed, leading to a predetermined phase orientation for the same polymer system. In certain aspects, after cross-linking, core-shell particles are stable in aqueous solutions and exhibit reproducible swelling behavior, while maintaining the original core-shell geometry.

Abstract: Methods and compositions for stabilizing the activity of catalytic compositions during catalytic processes, such as alkylation. A catalytic composition comprising a partially deactivated ionic liquid catalyst may be regenerated by reaction with a metal to form reactivated catalyst and an inorganic catalyst precursor; and the catalytic composition may be amended in-process by addition of an organic catalyst precursor for reaction with the inorganic catalyst precursor to form fresh ionic liquid catalyst. The organic catalyst precursor may be protected from water, e.g., during handling, by hydrophobic material(s).

Abstract: A fuel cell includes an electrode assembly, current collectors, and electroconductive separators. The electrode assembly includes an anode, a cathode, and a polymer electrolyte membrane arranged between the anode and cathode. The current collectors are arranged adjacent to the anode and cathode, respectively. The electroconductive separates are arranged outside the current collectors and have passages for feeding gases to the anode and cathode. The polymer electrolyte membrane includes an aromatic polymer having a sulfoalkylfluorene unit in its principal chain. An ion-exchange resin is used for the solid polymer electrolyte. An electrolyte membrane uses the ion exchange resin. A membrane/electrode assembly is used for the fuel cell.

Abstract: An anode provided with an electrocatalytic coating comprising tin, preferably tetravalent and in form of mixed oxide, prepared by the method for the manufacturing of an electrode, comprising applying a solution of a precursor for the pyrolytic formation of a tin-containing coating to a substrate of a valve metal, followed by the execution of thermal treatment, wherein the precursor solution comprises stannic hydroxychloride and a method of preparing the same.

Abstract: The invention relates to boron carbide and to a method for making the same, as well as to a super-abrasive material and a machine device including said boron carbide. The boron carbide of the invention has the following formula BC5 and has a diamond-type cubic structure with a mesh parameter a=3.635±0.006 &angst. The boron carbide of the invention can particularly be used in the field of machining.

Abstract: A configuration in which particles of pitch 2 having a softening point in the range of 70 to 200° C. and a diameter equal to or smaller than 30 ?m are held on the surfaces of particles of a refractory raw material 3 having a diameter equal to or smaller than 50 ?m is employed. This pitch-containing refractory raw material 1 can be used with the pitch being in a fine-particle form without any aggregation even after the long-term storage. Using it as a part of a raw material formulation allows the fine particles of pitch to be uniformly dispersed during the mixing or kneading process. The resulting carbon-containing refractory has an excellent corrosion resistance. It also provides suppressed increase in the Young's modulus while maintaining the level of strength, thereby being excellent in thermal spalling resistance even with the carbon content ratio being low.

Abstract: A method for converting a supported metal nitrate into the corresponding supported metal oxide comprises heating the metal nitrate to effect its decomposition under a gas mixture that contains nitric oxide and has an oxygen content of <5% by volume. The method provides very highly dispersed metal oxide on the support material. The metal oxide is useful as a catalyst or as a catalyst precursor.

Abstract: A phase change ink including (a) a phase change ink carrier and (b) a colorant comprising a carbon allotrope.

Abstract: A Ziegler-Natta procatalyst composition in the form of solid particles and comprising magnesium, halide and transition metal moieties, said particles having an average size (D50) of from 10 to 70 ?m, characterized in that at least 5 percent of the particles have internal void volume substantially or fully enclosed by a monolithic surface layer (shell), said layer being characterized by an average shell thickness/particle size ratio (Thickness Ratio) determined by SEM techniques for particles having particle size greater than 30 ?m of greater than 0.2.

Abstract: The invention relates to a method for removing heavy metal ions from the lattice of tectosilicates or phyllosilicates, especially from zeolite mineral, particularly clinoptilolite, by exchanging ions with calcium ions. According to the inventive method, the zeolite rock is brought in contact with hydrochloric and ammonium-containing solutions in a chain of exchange reactors such that a large part of the cations of the lattice are replaced with ammonium ions, and the ammonium ions located in the lattice are replaced with calcium in a basic calcium hydroxide solution. The ammonium or ammonia used in the process is conducted in the circuit by binding the same in hydrochloric acid as an ammonium ion from the exchange solutions by conveying anhydrous ammonia and can be fed back to the exchange solution. The ions from the lattice that are exchanged are essentially precipitated as phosphate, carbonate, or hydroxide.

Abstract: The present invention relates to a method for preparing iron-containing porous organic-inorganic hybrid materials where the organic compound ligand is bonded to a central metal and has a large surface area and pores of molecular size or nano size, by irradiating microwaves instead of heat treatments such as the conventional electric heating, etc. as the heat source of the hydrothermal or solvothermal synthesis reaction, after reacting a metal or metal salt and organic compound to form crystal nuclei by a predetermined pre-treatment operation in the presence of a solvent. In another aspect, a method of the present invention further comprises the step of purifying the obtained porous organic-inorganic hybrid materials by treating them with inorganic salt. In particular, a method of the present invention is characterized by not using a hydrofluoric acid.

Abstract: A method for recovering base metal values from oxide ore is provided, where the ore includes a first group metal selected from iron, magnesium and aluminum and a second group metal selected from nickel, cobalt and copper. The method includes reducing ore particle size to suit the latter unit operations, favoring contact of the metal elements, contacting the ore with ferric or ferrous chloride, hydrated or anhydrous, to produce a mix of ore and iron(II or III) chloride, subjecting the mixture of the ore and ferric or ferrous chloride to enough energy to decompose the chlorides into hydrochloric acid and a iron oxide, contacting the readily-formed hydrochloric acid with the base metal oxides from the second group, forming their respective chlorides, selectively dissolve the produced base metal chlorides, leaving the metals as oxides and in the solid state, and recovering the dissolved base metal values from aqueous solution.

Abstract: The invention provides a method of using an alcohol and a primary or secondary amine as the starting material to produce the corresponding secondary amine easily at a high yield and a catalyst used therein. The invention relates to a film-type catalyst for production of a tertiary amine, which is used in producing a tertiary amine from an alcohol and a primary or secondary amine as the starting material, and a process for producing a tertiary amine, which includes reacting an alcohol with a primary or secondary amine in the presence of the film-type catalyst.

Abstract: According to a first embodiment of a production method of an oxidation catalyst device for exhaust gas purification of the present invention, a plurality of slurries containing a catalyst precursor prepared from mutually different organic acids is coated respectively on a porous filter carrier (2) and calcined. According to a second embodiment of the present invention, the slurry contains the catalyst precursor having a particle diameter distribution ranging from 0.5 to 10 ?m, and the slurry has a viscosity equal to or below 2.0 mPa·s. The oxidation catalyst device of the present invention is composed of a composite metal oxide on a surface of a cell division and a surface of an air pore of the porous filter carrier having a wall-flow structure.

Abstract: Gas generation of a non-aqueous electrolyte battery having a negative active material that intercalates/deintercalates lithium ions at a potential not lower than 1.2 V relative to the potential of lithium as negative electrode is suppressed. A non-aqueous electrolyte battery comprising a non-aqueous electrolyte containing an electrolyte salt and a non-aqueous solvent, a positive electrode and a negative electrode is characterized in that the main active material of said negative electrode is an active material that intercalates/deintercalates lithium ions at a potential not lower than 1.2 V relative to the potential of lithium and the auxiliary active material of said negative electrode is an active material that at least intercalates lithium ions at a potential lower than 1.