Abstract: A hydrogen generation apparatus employs a thermocatalytic reactor (60) formed of a top plate (62), a bottom plate (66), and a reactor core (64) disposed between the top an bottom plates. The reactor core has a reaction surface (64a) and a combustion surface (64b), each surface having a raised periphery defining opposing ends (61a and 61b) and opposing sides (63a and 63b). The reaction surface (64a) and the top plate (62) together define a reaction chamber and the combustion surface (64b) and the bottom plate (66) together define a combustion chamber. The reaction core (64) has a first set of a plurality of spaced apart, substantially straight radiating fins (76a) extending from the reaction surface (64a) and a second set of a plurality of spaced part, substantially straight radiating fins (76b) extending from the combustion surface (64b).

Abstract: The present disclosure provides teachings relating to ammonia-based hydrogen generation apparatus and associated methods of use. Exemplary methods and apparatus comprise a thermocatalytic hydrogen generation reactor which includes a reaction chamber containing a catalyst-coated substrate, and a combustion chamber containing a catalyst-coated substrate. Exemplary catalyst-coated substrates include, but are not limited to, metal foam, monolith, mesh, ceramic foam or ceramic monolith.

Abstract: A subject matter of the present invention is compositions which generate nitrogenous gas, with a low decomposition temperature, and processes for the generation of nitrogenous gas comprising the decomposition of such compositions. Said compositions comprise: from 20 to 80% by weight of azodicarbonamide, from 20 to 80% by weight of a nitrogenous reducing charge, from 0 to less than 10% by weight of at least one additive; said azodicarbonamide and said nitrogenous reducing charge representing at least 90% of their weight and said nitrogenous reducing charge comprising: at least one compound from a first family of reducing components chosen from tetrazole, tetrazole derivatives and their salts, salts of bitetrazole and of its derivatives, 5,5?-azobitetrazole salts, polyvinyltetrazoles and their mixtures; and/or at least one compound from a second family of reducing components chosen from dicyandiamide, 1-hydrobenzotriazole, silicon nitride, nitroguanidine, guanidine nitrate and their mixtures.

Abstract: A method of producing hard wear resistant layer with improved wear resistance. The method is a reactive arc-evaporation based process using a cathode including as main constituent at least one phase of a refractory compound Mn+1AXn (n=1, 2 or 3), wherein M is one or more metals selected from the groups IIIB, IVB, VB, VIIB and VIIB of the periodic table of elements, A is one or more elements selected from the groups IIIA, IVA, VA and VIA of the periodic table of elements, and wherein X is carbon and/or nitrogen.

Abstract: A nitride crystal is characterized in that, in connection with plane spacing of arbitrary specific parallel crystal lattice planes of the nitride crystal obtained from X-ray diffraction measurement performed with variation of X-ray penetration depth from a surface of the crystal while X-ray diffraction conditions of the specific parallel crystal lattice planes are satisfied, a uniform distortion at a surface layer of the crystal represented by a value of |d1-d2|/d2 obtained from the plane spacing d1 at the X-ray penetration depth of 0.3 ?m and the plane spacing d2 at the X-ray penetration depth of 5 ?m is equal to or lower than 2.1×10?3.

Abstract: A luminescent particle includes an interior portion of the luminescent particle comprising a luminescent compound that reacts with atmospherically present components and a passivating layer on an outer surface of the luminescent particle that is operable to inhibit the reaction between the luminescent compound and the atmospherically present components.

Abstract: The invention is directed to a solid, porous material, suitable for generating nitrogen gas, said material having a porosity of 20 to 75 vol. %, and a composition comprising, based on the weight of the material of 60 to 90 wt. % of sodium azide, 0.1 to 20 wt. % of an inert chemical coolant based on at least one inorganic salt having a heat capacity of at least 1400 J/K/kg, 0.1 to 20 wt. % of modifying agent selected from metal oxides and metal carbonates, and a binder, selected from the group consisting of at least one alkali metal silicate, preferably waterglass, or a poly-tetrazole, in an amount of between 3 and 15 wt. %.

Abstract: A method for concentrating effectively the heavy nitrogen isotope 15N to 50 atom % or more in which 14N15N and/or 15N2, which are molecules containing a heavy nitrogen isotope of 15N, are concentrated by distilling successively nitrogen N2 using plural distillation columns T1 to T4 each of which includes at least one condenser C1 to C4 and at least one reboiler R1 to R4 and is arranged in series, and a part of nitrogen in the distillation is drawn out to be subjected to isotope scrambling in an isotope scrambler S1, and nitrogen after the isotope scrambling is returned to the distillation to produce nitrogen N2 with a 15N concentration of 50 atom % or more.

Abstract: The present invention relates to a process of enriching element content in stable isotopes of light elements in ion-exchange chromatography. The process comprises development of band of light elements in a chromatographic column; elution of said band in a discontinuous basis so as to disconnect said chromatographic column at particular stage; and finally the process comprises of regeneration step.

Abstract: A bioreactor designed to produce N2O from organic nitrogen and/or reactive nitrogen in waste is coupled to a hardware reactor device in which the N2O is consumed in a gas phase chemical reaction, e.g., catalytic decomposition to form oxygen and nitrogen gas. Heat from the exothermic reaction may be used to generate power. The bioreactor may use communities of autotrophic microorganisms such as those capable of nitrifier denitrification, ammonia oxidizing bacteria, and/or ammonia oxidizing archaea. A portion of the N2O dissolved in aqueous effluent from the bioreactor may be separated to increase the amount of gas phase N2O product. The amount of the gas phase N2O in a gas stream may also be concentrated prior to undergoing the chemical reaction. The N2O may alternatively be used as an oxidant or co-oxidant in a combustion reaction, e.g., in the combustion of methane.

Abstract: An apparatus of generating fluorinated gas compounds by means of reacting liquid stock with gaseous material is characterized by providing a circulating system comprised of a reaction chamber where a liquid mixture containing the liquid stock reacts with the gaseous material, a fluid conduit through which the liquid mixture alone flows, an upper fluid channel through which the reacted liquid mixture moves from the top of the reaction chamber to the top of the fluid conduit, and a lower fluid channel through which the liquid mixture moves from the bottom of the fluid conduit to the bottom of the reaction chamber, and sparging into the bottom of the reaction chamber (A) the virgin gaseous material and (B) at least one selected from the fluorinated gas compounds resulted from the reaction in the reaction chamber, including the first fluorinated gas product generated in the first cycle of the reaction and the second or later gas product resulted from further fluorinating the first or later gas product in the succ

Abstract: A colloidal suspension of III-V semiconductor nanoparticles.

Abstract: A method of fractionating biomass, by permeability conditioning biomass suspended in a pH adjusted solution of at least one water-based polar solvent to form a conditioned biomass, intimately contacting the pH adjusted solution with at least one non-polar solvent, partitioning to obtain an non-polar solvent solution and a polar biomass solution, and recovering cell and cell derived products from the non-polar solvent solution and polar biomass solution. Products recovered from the above method. A method of operating a renewable and sustainable plant for growing and processing algae.

Abstract: This invention provides a comprehensive solution which comprises the production of a bed of ash-containing hot char via the pyrolysis of coal which generates a hydrogen rich gas that, subsequent to its cleanup, can be synthesized into chemicals and/or transportation fuels, while the hot char is used to: (i) reduce SO2 and NOX to elemental sulfur and to elemental nitrogen, respectively; (ii) react hot char with CO2 to reduce it to CO, a valuable chemical that can be converted into fertilizer or into a fuel gas that can be used for electric or thermal power generation; (iii) trap particulate matter in the bed of char to join the ash in the char to form a combined ash which is eventually converted to inert slag; and (iv) filter the mercury through a portion of the char to prevent it from being emitted into the atmosphere.

Abstract: A reversible hydrogen storage composition having an empirical formula of: Li(x+z)NxMgyBzHw where 0.4?x?0.8; 0.2?y?0.6; 0<z?0.4, x+y+z=1 and “w” varies from 0 to 2x+2y+4z. This composition shows greater low temperature reversible hydrogen storage compared to binary systems such as MgH2—LiNH2.

Abstract: The invention provides a method for the combined production of (i) a fertilizer selected from the group consisting of ammonium nitrate, ammonium phosphates or a combination thereof, (ii) a concentrated stream of CO2 through an indirect neutralization of ammonia with an acid selected from the group consisting of nitric acid, phosphoric acid, a salt thereof and a combination thereof; said method comprising: (I) reacting a carbonate product with a reagent selected from the group consisting of nitric acid, phosphoric acid, a salt thereof, and a mixture thereof to form CO2, and a fertilizer containing an ammonia component; and (II) separating at least a portion of said carbon dioxide from said fertilizer in a condensed and relatively concentrated stream.

Abstract: A manufacturing method of a nitride crystalline film includes following steps. First, a substrate is provided. Next, a first nitride crystalline film is formed on the substrate. A patterned mask is then formed on the first nitride crystalline film. The patterned mask covers a first part of the first nitride crystalline film and exposes a second part of the first nitride crystalline film. Afterwards, the second part is etched, and the first part is maintained. After that, the patterned mask is removed. The first part is then etched to form a plurality of nitride crystal nuclei. Next, a second nitride crystalline film is formed on the substrate, and the second nitride crystalline film is made to cover the nitride crystal nuclei. A nitride film and a substrate structure are also provided.

Abstract: State-of-the-art electronic structure calculations provide the likelihood of the availability of YLi3N2, ZrLi3N2, NbLi3N2, MoLi3N2, TcLi3N2, RuLi3N2, RhLi3N2, GeLi3N2, InLi3N2, and SnLi3N2 as compounds for reaction with hydrogen under suitable conditions. Such calculations also provide the likelihood of the availability of YLi3N2Hn, ZrLi3N2Hn, NbLi3N2Hn, MoLi3N2Hn, TcLi3N2Hn, RuLi3N2Hn, RhLi3N2Hn, PdLi3N2Hn, AgLi3N2Hn, CdLi3N2Hn, AlLi3N2Hn, GaLi3N2Hn, GeLi3N2Hn, InLi3N2Hn, SnLi3N2Hn, and SbLi3N2H, (here n is an integer having a value of 1-6) as solid hydrides for the storage of hydrogen. These materials offer utility for hydrogen storage systems.

Abstract: Devices and components that can interact with or modify propagation of electromagnetic waves are provided. The design, fabrication and structures of the devices exploit the properties of reactive composite materials (RCM) and reaction products thereof.

Abstract: A semiconductor device including a metallic compound Hfx1Moy1Nz1 as an electrode. The work function of the electrode can be modulated by doping the metallic compound with dopants including nitrogen, silicon or germanium. The metallic compound of the present invention is applicable to PMOS, NMOS, CMOS transistors and capacitors.

Abstract: A method for producing fine silver particles which is characterized by making an aqueous silver ammine complex solution and a reducing agent solution come in contact with each other in an open space to reduce the silver ammine complex and deposit fine silver particles, either in which the contacting is conducted by (i) a method of spraying an aqueous silver ammine complex solution and a reducing agent solution through nozzles or (ii) a method of discharging an aqueous silver ammine complex solution and a reducing agent solution from obliquely downward nozzles opposite to each other to thereby produce fine silver particles which are free from coarse particles having particle sizes of 5 ?m or more and have a mean particle size of primary particles of 0.08 to 1.0 ?m and crystallite sizes of 20 to 150 nm or in which an aqueous silver ammine complex solution having a silver concentration of 20 to 180 g/L and an organic reducing agent solution having a reducing agent concentration of about 0.6 to about 1.

Abstract: Provided is a thermal expansion inhibitor which has a much broader application range and which can be used with ease. Used is a thermal expansion inhibitor comprising a manganese nitride crystal.

Abstract: A method of recovering carbon dioxide from a synthesis gas stream generated within a synthesis gas facility. After the synthesis gas stream is passed through at least one process heat exchanger of the steam generation system located downstream of the water-gas shift reactor, the temperature of the synthesis gas stream is increased while simultaneously adding steam to the synthesis gas stream. Thereafter, the synthesis gas stream is added to an absorption system having an absorption zone utilizing a solvent to absorb the carbon dioxide and a regeneration zone to disengage the carbon dioxide from the solvent and thereby regenerate the solvent. Heat is transferred from the synthesis gas stream to the regeneration zone to promote disengagement of the carbon dioxide from the steam and such that between about 40 percent and about 90 percent of the carbon dioxide originally present in the synthesis gas stream is recovered.

Abstract: A hydrothermally stable, microporous organic-inorganic hybrid membrane based on silica, having an mean pore diameter of between 0.2 and 1.5 nm, is characterised in that between 5 and 40 mole % of the Si—O—Si bonds have been replaced by moieties having the one of the formulas: Si—{[CmH(n-1)X]—Si—}q, Si—[CmH(n-2)X2]—Si or Si—CmHn—Si{(CmHn)—Si—}y in which m=1-8, n=2m, 2m-2, 2m-4, 2m-6 or 2m-8; provided that n?2, X=H or (CH2)pSi, p=0 or 1, and q=1, 2, 3 or 4. The membrane can be produced by acid-catalysed hydrolysis of suitable bis-silane precursors such as bis(trialkoxysily)alkanes, preferably in the presence of monoorganyl-silane precursors such as trialkoxy-alkylsilanes.

Abstract: In various embodiments, the present disclosure provides a method of fixing nitrogen. An amount of titania catalyst is provided and contacted with a feed stream that includes nitrogen. The titania catalyst is heated. The heated titania catalyst fixes nitrogen in the feed stream to form nitrogen products, such as nitrates. The nitrogen products are then removed from the titania catalyst. In some examples, the titania catalyst is treated with a base. In further examples, the catalytic process is carried out in the absence of light for photochemically activating the titania catalyst.

Abstract: The invention relates to a method of separating fluids from mixtures using a zeolite known as ITQ-32 consisting of a two-dimensional pore system comprising channels with openings formed by 8 tetrahedra which are interconnected by channels with openings formed by 12 tetrahedra. The inventive method comprises at least the following steps: a) the zeolite ITQ-32 material is brought into contact with the mixture of fluids, b) one or more of the components are adsorbed in the zeolite ITQ-32 material, c) the non-adsorbed components are extracted, and d) one or more of the components adsorbed in the zeolite ITQ-32 material are recovered.

Abstract: The detecting and monitoring of solid structure or phase transformation, such as those used for testing the formation of gas hydrates and their inhibition by chemical additives may be conducted in a multi-test assembly of laboratory bench scale loops. The test loop contains a fluid that includes water and hydrate-forming guest molecules such as methane, ethane, carbon dioxide and the like at hydrate-forming conditions of low temperature and high pressure. A small bit or “pig” may be circulated through the test loop at variable speeds. The pig may be moved or impelled through the test loop remotely. The formation of hydrates may be monitored with consistent and reproducible results.

Abstract: Provided is a production method for producing a solid product by a reaction of gaseous raw materials with a plurality of components including a step of conducting the reaction using a reactor disposed in a vertical direction; a step of feeding the gaseous raw materials with a plurality of components from the upper part of the reactor; a step of, in the lower part of the reactor, forming a seal gas layer composed of a gas having a high density and fed continuously from the lower part of the reactor; a step of discharging an exhaust gas containing a by-product gas generated by the reaction and unreacted gaseous raw materials from somewhere in the upper part of the formed seal gas layer; and a step of accommodating a solid product in the seal gas layer of the lower part.

Abstract: A nitridosilicate-based compound is produced by reacting an alkaline-earth metal compound capable of generating an alkaline-earth metal oxide by heating or a rare earth compound capable of generating a rare earth oxide by heating with at least a silicon compound, while the alkaline-earth metal compound or the rare earth compound is being reduced and nitrided by the reaction with carbon in an atmosphere of nitriding gas. Because of this, a nitridosilicate-based compound of high quality can be produced industrially at low cost.

Abstract: An electrode material for an anode of a rechargeable lithium battery, containing a particulate comprising an amorphous Sn.A.X alloy with a substantially non-stoichiometric ratio composition. For said formula Sn.A.X , A indicates at least one kind of an element selected from a group consisting of transition metal elements, X indicates at least one kind of an element selected from a group consisting of O, F, N, Mg, Ba, Sr, Ca, La, Ce, Si, Ge, C, P, B, Pb, Bi, Sb, Al, Ga, In, Tl, Zn, Be, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, As, Se, Te, Li and S, where the element X is not always necessary to be contained. The content of the constituent element Sn of the amorphous Sn.A.X alloy is Sn/(Sn+A+X)=20 to 80 atomic %.

Abstract: In order to reduce incoming atmospheric carbon dioxide levels in compressed air prior to cryogenic distillation, a water spray cooling tower equipped with biocatalytic packing, or fed with absorptive reagents, is used to convert gaseous carbon dioxide into bicarbonate ions which dissolve in the cooling water. The hydration reaction and refrigeration occur synergistically. The bicarbonate ions are subsequently removed from the solution using the heat from the compressed air in a regenerator re-boiler unit, and then fed to a percolation cooling tower for releasing CO2 and cooling.

Abstract: The efficiency of an etching process may be increased in various ways, and the cost of an etching process may be decreased. Unused etchant may be isolated and recirculated during the etching process. Etching byproducts may be collected and removed from the etching system during the etching process. Components of the etchant may be isolated and used to general additional etchant. Either or both of the etchant or the layers being etched may also be optimized for a particular etching process.

Abstract: A process for synthesizing a halogenated nitrogen represented by a formula of NFxL3-x, where L represents a halogen other than fluorine, and 1?x?3 is provided. This process includes the step of (a) reacting an ammonium complex compound that is one selected from the group consisting of NH4F.nHF, (NH4)yMFz.mHF and a mixture of these and that is in liquid form, with an interhalogen compound or a mixture of an interhalogen compound and F2 gas, wherein 1<n, 1?y?4, 2?z?8, 0.1?m, and M represents one selected from the group consisting of elements of group 1 to group 16 of periodic table and a mixed element of these elements.

Abstract: The invention relates to a process for the incorporation of nanophosphors (phosphors) into micro-optical structures, and to corresponding illuminants. In this impregnation process, a micro-optical system comprising inverse opal powders is filled with a dispersion of a nanophosphor.

Abstract: A method of forming Mn+1AXn, where M is an early transition metal (such as Ti) or mixtures thereof, A is a group III or IV element (such as Si) or mixtures thereof and X is C, N or mixtures thereof, the method comprising the steps of providing a precursor of formula Mn+1AXn and reacting the Mn+1Xn with A to provide Mn+1AXn. The Mn+1Xn may be ordered and/or twinned (eg by mechanical alloying, thermal treatment etc. prior to reacting with A, ordered and/or twinned during its formation from M and X. A may be present during the formation of Mn+1Xn from M and X or during the ordering and/or twinning of disordered Mn+1Xn. The Mn+1AXn produced is substantially free from MX and or other residual phases.

Abstract: Provided is a thermal expansion inhibitor which has a much broader application range and which can be used with ease. Used is a thermal expansion inhibitor comprising a manganese nitride crystal.

Abstract: The invention uses a feed of atmospheric air and mixes the air with hydrogen. The hydrogen and air mixture is fed into a catalytic reactor where a deoxygenation reaction occurs. The deoxygenation reaction uses a platinum catalyst to produce water from oxygen and hydrogen. The nitrogen passes through the catalytic reactor without reacting with the hydrogen, the oxygen, or the water. The water is separated from the nitrogen in a dryer. The nitrogen may then be used in drilling and production operations. The water is fed into an electrolyzer where an electrolysis reaction occurs. The electrolyzer passes an electrical current through the water to produce gaseous oxygen and hydrogen. The hydrogen is recycled back to the catalytic reactor and the oxygen may be vented or sold.

Abstract: State-of-the-art electronic structure calculations provide the likelihood of the availability of YLi3N2, ZrLi3N2, NbLi3N2, MoLi3N2, TcLi3N2, RuLi3N2, RhLi3N2, GeLi3N2, InLi3N2, and SnLi3N2 as for reaction with hydrogen under suitable conditions. Such calculations also provide the likelihood of the availability of YLi3N2Hn, ZrLi3N2Hn, NbLi3N2Hn, MoLi3N2Hn, TcLi3N2Hn, RuLi3N2Hn, RhLi3N2Hn, PdLi3N2Hn, AgLi3N2Hn, CdLi3N2Hn, AlLi3N2Hn, GaLi3N2Hn, GeLi3N2Hn, InLi3N2Hn, SnLi3N2Hn, and SbLi3N2H, (here n is an integer having a value of 1-6) as solid hydrides for the storage of hydrogen. These materials offer utility for hydrogen storage systems.

Abstract: An AlxGayIn1-x-yN substrate in which particles having a grain size of at least 0.2 ?m on a surface of the AlxGayIn1-x-yN substrate are at most 20 in number when a diameter of the AlxGayIn1-x-yN substrate is two inches, and a cleaning method with which the AlxGayIn1-x-yN substrate can be obtained are provided. Further, an AlxGayIn1-x-yN substrate in which, in a photoelectron spectrum of a surface of the AlxGayIn1-x-yN substrate by X-ray photoelectron spectroscopy with a detection angle of 10°, a ratio between a peak area of C1s electrons and a peak area of N1s electrons (C1s electron peak area/N1s electron peak area) is at most 3, and a cleaning method with which the AlxGayIn1-x-yN substrate can be obtained are provided.

Abstract: A catalyst composition and a process for using it to decompose nitrous oxide into nitrogen and oxygen are disclosed. The catalyst composition has surface area of about 1 to about 200 m2/g after exposure to a calcination temperature of between about 400° C. and about 900° C., or about 1 to about 100 m2/g after exposure to a calcination temperature of between about 400° C. and about 950° C.

Abstract: A nitride crystal is characterized in that, in connection with plane spacing of arbitrary specific parallel crystal lattice planes of the nitride crystal obtained from X-ray diffraction measurement performed with variation of X-ray penetration depth from a surface of the crystal while X-ray diffraction conditions of the specific parallel crystal lattice planes are satisfied, a uniform distortion at a surface layer of the crystal represented by a value of |d1?d2|/d2 obtained from the plane spacing d1 at the X-ray penetration depth of 0.3 ?m and the plane spacing d2 at the X-ray penetration depth of 5 ?m is equal to or lower than 2.1×10?3.

Abstract: A method and system of providing compressed substantially oxygen-free exhaust gas for industrial purposes including the steps of extracting exhaust gas from a lean burn engine consuming a mixture of natural gas fuel and air, passing the extracted exhaust gas through a cooling step to cause entrained water vapor therein to condense out, separating and disposing of the condensed water, measuring the oxygen content of the exhaust gas, using the measurement to regulate the quantity of natural gas fed into an igniter into which the exhaust gas is also fed so that substantially all of the oxygen in the exhaust gas is consumed by combustion with the natural gas in the igniter to provide at an outlet of the igniter substantially oxygen-free exhaust gas, and compressing the substantially oxygen-free exhaust gas to provide compressed exhaust gas for industrial applications.

Abstract: Floating slow-release fertilizer is designed to significantly reduce carbon dioxide in the atmosphere. This granulated fertilizer has a density lighter than seawater. Therefore its pellets can float on the surface of seawater. After being dispensed into water, the pellets are able to continually release certain nutrients for a period of time. During this period, an otherwise inanimate water region is temporarily suitable for plant growth. Floating slow-release fertilizer enables the growth of planting phytoplankton in ocean to remove CO2 from atmosphere. The advantages of the fertilizer are as following: all nature, effective, no byproduct, no land using, no pollution, using solar energy mainly, small investment, easy to control, low operation cast.

Abstract: Crystalline scintillator materials comprising nano-scale particles of metal halides are provided. The nano-scale particles are less than 100 nm in size. Methods are provided for preparing the particles. In these methods, ionic liquids are used in place of water to allow precipitation of the final product. In one method, the metal precursors and halide salts are dissolved in separate ionic liquids to form solutions, which are then combined to form the nano-crystalline end product. In the other methods, micro-emulsions are formed using ionic liquids to control particle size.

Abstract: The present invention is directed to carbon monoxide oxidation reactions in the presence of an O2 containing gas, nitrogen oxide conversion reactions, volatile organic compound conversion reactions in the presence of an O2 containing gas, and combinations thereof, and catalysts for use in those reactions. The catalyst comprises cobalt, its oxides or mixtures thereof and ruthenium, its oxides or mixtures thereof.

Abstract: The invention provides methods, compositions, and systems for a reversible hydrogen storage material. The hydrogen storage material contains a lithium-magnesium compound, having LiMgN in a dehydrogenated state and a hydrogenated lithium magnesium product in a hydrogenated state, where the hydrogenated and dehydrogenated states are reversible. The lithium-magnesium compound is formed by reacting MgH2 and LiNH2 in a substantially inert atmosphere in amounts sufficient to obtain a hydrogen adsorption of at least 3 wt %, and in many cases up to about 8.1 wt %.

Abstract: This invention relates to a solid divided composition comprising grains whose mean size is greater than 25 ?m and less than 2.5 mm, wherein each grain is provided with a solid porous core and a homogeneous continuous metal layer consisting of at least one type of transition non-oxidised metal and extending along a gangue coating the core in such a way that pores are inaccessible. A method for the production of said composition and for the use thereof in the form of a solid catalyst is also disclosed.

Abstract: The present invention provides a method and a system for stripping volatile compounds such as ammonia from liquids. Part of the ammonia is stripped from the liquid in a system having a shunt through which liquid such as e.g. fermented biomass can be diverted in the form of a side stream in liquid contact with a main fermentor(s). The stripper system is connected to an evaporator. In the evaporator aqueous liquid is heated at a pressure below atmospheric pressure whereby vapor is developed at a temperature below 100° C. The vapor from the evaporator is directed to the liquid medium containing ammonia and this results in ammonia being stripped from the liquid and transferred to the vapor phase. The vapor phase is condensed in a first condenser at a low pressure, and the liquid thus obtained is further treated in a stripper unit at a higher pressure.

Abstract: A III-V nitride, e.g., GaN, substrate including a (0001) surface offcut from the <0001> direction predominantly toward a direction selected from the group consisting of <10-10> and <11-20> directions, at an offcut angle in a range that is from about 0.2 to about 10 degrees, wherein the surface has a RMS roughness measured by 50×50 ?m2 AFM scan that is less than 1 nm, and a dislocation density that is less than 3E6 cm?2. The substrate may be formed by offcut slicing of a corresponding boule or wafer blank, by offcut lapping or growth of the substrate body on a corresponding vicinal heteroepitaxial substrate, e.g., of offcut sapphire. The substrate is usefully employed for homoepitaxial deposition in the fabrication of III-V nitride-based microelectronic and opto-electronic devices.

Abstract: The invention pertains to a layered ammonia oxidation catalyst. The layered catalyst causes ammonia to be selectively oxidized in the presence of an oxidant such as air, while minimizing the formation of nitrogen oxides (NOx). The layered catalyst comprises a refractory oxide support such as gamma alumina upon which a platinum component is deposited and a vanadia component is deposited on the platinum. The catalyst is preferably disposed on a substrate such as a metal foil whose surface contains a “herringbone” pattern.