Abstract: Disclosed is a method for preparing a bimetallic perovskite loaded grapheme-like carbon nitride photocatalyst, comprising: 11) dissolving SbCl3 and AgCl in HCl solution under heating and constant stirring; then adding CsCl in the heated solution to form sediment on the bottom of the beaker; collecting the sediment and wash it with ethanol, and finally drying in an oven to obtain Cs2AgSbCl6 powder; 12) adding melamine into an aluminum oxide crucible and placing it into a muffle furnace for calcination and finally cooling to room temperature naturally to obtain g-C3N4 samples; 13) adding the Cs2AgSbCl6 bimetallic perovskite and the g-C3N4 into a solvent, and stirring after subjecting to ultrasound, and drying after centrifuging to obtain the photocatalyst. Provided is a new idea for the combination of bimetallic halide perovskite and photocatalytic material, and the preparation method has mild conditions, simple operation, and is favorable for large-scale production.

Abstract: A method for preparing a support for an electrode catalyst including forming first and second polymer layers having charges different from each other on a surface of a carbon support and carbonizing the result, wherein the polymers included in the first and the second polymer layers are an aromatic compound including a heteroatom, and the first or the second polymer includes a pyridine group.

Abstract: Methods for forming a rhenium-containing film on a substrate by a cyclical deposition are disclosed. The method may include: contacting the substrate with a first vapor phase reactant comprising a rhenium precursor; and contacting the substrate with a second vapor phase reactant. Semiconductor device structures including a rhenium-containing film formed by the methods of the disclosure are also disclosed.

Abstract: Catalysts for producing a branched aliphatic alkene are described. The catalyst can include a catalytic alkali metal or alkali metal composite on a mixed metal oxide support that includes a Column 1 metal and at least one of a Column 3 metal, a Column 4 metal or a lanthanide. The catalyst can have less than 50 wt. % of a metal carbonate. Methods of producing branched aliphatic alkenes by contacting the catalyst of the present invention with an aliphatic alpha olefin are also described.

Abstract: A system for oxidative conversion of a mixed hydrocarbon feed stream to a product stream containing at least one olefin is provided. The system includes a plurality of reactors each capable of oxidatively dehydrogenating at least a portion of a hydrocarbon in the mixed hydrocarbon feed, and each reactor able to operate at different set of reaction conditions from other reactors in the plurality of reactors. All of the reactors use the same oxygen transfer agent to produce at least one olefin. In some embodiments, at least one reactor is optimized to oxidatively couple methane to produce ethylene, while other reactors are optimized to oxidatively dehydrogenate ethane to ethylene or to oxidatively dehydrogenate propane to ethylene and/or propylene. All of the reactors feed into a single regeneration unit for the oxygen transfer agent. A method of oxidatively converting the mixed hydrocarbon feed to an olefin is also provided.

Abstract: Provided is a porous material which is not easily damaged even when being exposed to a high temperature in a low oxygen atmosphere, and has heat resistance improved. A porous material includes aggregates formed of a nonoxide containing silicon and a binding material formed of an oxide ceramic binding the aggregates to each other while keeping a plurality of pores. The porous material has a phase containing oxygen on a surface of the aggregates including a boundary surface with the binding material. In the porous material, a content ratio of oxygen in the aggregates is preferably from 2 to 25% by mass relative to the mass of the aggregates.

Abstract: Processes for manufacturing nitrogen oxide storage materials and lean NOx trap catalysts are disclosed. Also disclosed are nitrogen oxide storage material made by processes comprising barium carbonate (BaCO3) and ceria (CeO2) by using Ba(OH)2 instead of most or all Ba(OOCH3)2 to reduce cost and reduce harmful byproducts. Aspects of the present invention also relate generally to lean NOx trap (LNT) comprising nitrogen oxide storage materials.

Abstract: Butadiene is made from a butene rich feed by passing a superheated butene rich feed including superheated steam and oxygen at a temperature of at least about 343° C. (650° F.) over a catalyst bed having a depth of over about 69 cm (27 inches) of granules of ferritic oxidative dehydrogenation catalyst. Inlet conditions being controlled such that the oxidative dehydrogenation reactions initially occur in the lower most layers of catalyst. Process control includes monitoring the temperature throughout the bed and increasing the inlet temperature in response to a drop in the temperature in the active layer, when the active layer of oxidative dehydrogenation catalyst begins to become deactivated so that the reaction zone moves upwardly in the oxidative dehydrogenation bed.

Abstract: A catalyst comprising a Group IIIA metal, a Group VIII noble metal, and an optional promoter metal, on a support selected from silica, alumina, silica-alumina compositions, rare earth modified alumina, and combinations thereof, doped with iron, a Group VIB metal, a Group VB metal, or a combination thereof, offers decreased reactivation time under air soak in comparison with otherwise identical catalysts. Reducing reactivation time may, in turn, reduce costs, both in inventory and capital.

Abstract: A catalyst consisting of structurally ordered mesoporous carbon containing a transition metal and a method for preparing the same are provided. The method for preparing the catalyst includes forming a mixture of a carbon precursor and structurally ordered mesoporous silica, carbonizing the mixture to form a composite, and removing mesoporous silica from the composite.

Abstract: A catalyst comprising palladium, bismuth, and at least one third element X selected from the group consisting of P, S, Sc, V, Ga, Se, Y, Nb, Mo, La, Ce, and Nd, wherein the catalyst further comprises a support.

Abstract: The purpose of the present invention is to provide a spherical or ellipsoidal magnesium alcoholate having a narrow particle size distribution even when the particle size is small. The present invention provides a method for producing a magnesium alcoholate by adding in a portionwise manner to a reaction system and reacting, metallic magnesium, an alcohol, and at least one of a halogen or a halogen atom-containing compound in the reaction system under alcohol reflux, which is a method for producing a magnesium alcoholate characterized in that a mixture of metallic magnesium, an alcohol, and at least one of a halogen or a halogen atom-containing compound is added to the reaction system at each portionwise addition.

Abstract: Surfaces of silicone particles are hydrophilized by plasma treatment. The hydrophilized silicone particles are readily dispersible in aqueous materials without a need for dispersants, typically surfactants. In aqueous cosmetic applications externally applied to the skin such as skin care cosmetics, make-up cosmetics, antiperspirant cosmetics, and UV care cosmetics, for example, products free of skin irritation concern can be formulated because formulation is possible without a need for surfactants.

Abstract: Using conventional synthesis methods, when an unsaturated carboxylic acid or a derivative thereof is synthesized from a hydroxycarboxylic acid or a derivative thereof by a dehydration reaction using a catalyst, the yield has been low. Accordingly, an object of the present invention is to provide a catalyst capable of synthesizing unsaturated carboxylic acids or derivatives thereof by a dehydration reaction that produces a high yield. The synthetic catalyst comprises an apatite compound containing an alkali metal in a crystal structure thereof, and the invention further includes methods for synthesizing an unsaturated carboxylic acid and/or a derivative thereof. The methods comprise contacting the aforementioned synthetic catalyst with the hydroxycarboxylic acid and/or a derivative thereof, so as to synthesize the unsaturated carboxylic acid and/or a derivative thereof by a dehydration reaction.

Abstract: A composition for oxidizing dimethyl ether includes an alloy supported on carbon, the alloy being of platinum, ruthenium, and palladium. A process for oxidizing dimethyl ether involves exposing dimethyl ether to a carbon-supported alloy of platinum, ruthenium, and palladium under conditions sufficient to electrochemically oxidize the dimethyl ether.

Abstract: The electrocatalyst for the electrochemical conversion of carbon dioxide includes a copper material supported on titania nanotubes. The copper material may be pure copper, copper and ruthenium, or copper and iron supported on the titania nanotubes. The electrocatalyst is prepared by first dissolving copper nitrate trihydrate in deionized water to form a salt solution. Titania nanotubes are then added to the salt solution to form a suspension, which is then heated. A urea solution is added to the suspension to form the electrocatalyst in solution. The electrocatalyst is then removed from the solution. In addition to dissolving the copper nitrate trihydrate in the volume of deionized water, either iron nitrate monohydrate or ruthenium chloride may also be dissolved in the deionized water to form the salt solution.

Abstract: The invention is directed in a first aspect to a sulfur-carbon composite material comprising: (i) a bimodal porous carbon component containing therein a first mode of pores which are mesopores, and a second mode of pores which are micropores; and (ii) elemental sulfur contained in at least a portion of said micropores. The invention is also directed to the aforesaid sulfur-carbon composite as a layer on a current collector material; a lithium ion battery containing the sulfur-carbon composite in a cathode therein; as well as a method for preparing the sulfur-composite material.

Abstract: The present disclosure is directed to a desulphurisation agent for removing sulphurous species from a diluent or process stream, and a use of such agent. In some examples, the agent may include a compound of manganese, pore forming particles and a compound of copper. The agent may be introduced into or mixed with the diluent or process stream to effectuate removal of sulphorous species from the diluent or process stream.

Abstract: Disclosed is an alloy of the formula: Fe3?xAl1+xMyTzTat wherein M represents at least one catalytic specie selected from the group consisting of Ru, Ir, Pd, Pt, Rh, Os, Re and Ag; T represents at least one element selected from the group consisting of Mo, Co, Cr, V, Cu, Zn, Nb, W, Zr, Y, Mn, Cd, Si, B, C, O, N, P, F, S, CI, Na and Ti; and Ta represents tantalum. Such an alloy can be used as an electrode material for the synthesis of sodium chlorate. It can also be used as a coating for protection against corrosion.

Abstract: An object of the present invention is to provide a fuel cell electrode catalyst with which high durability and a high maximum output density are obtained even when a fuel cell is continuously operated for long time; a method for producing the fuel cell electrode catalyst; a fuel cell in which the catalyst is used; and the like. A method for producing a fuel cell electrode catalyst is provided, the method including: a step of preparing a catalyst precursor comprising each atom of a metal element, carbon, nitrogen, and oxygen, and comprising copper as the metal element; and a contact step of bringing the catalyst precursor and an acid solution into contact with each other to obtain a catalyst.

Abstract: The creation of a catalyst that can be used for a wide variety of applications including the steps of developing preliminary information regarding the catalyst, using the preliminary information to produce a template of the catalyst, and using the template of the catalyst to produce the catalyst.

Abstract: An object of the present invention is to suppress flooding phenomenon in an electrode catalyst for fuel cells containing a metal atom, a carbon atom, a nitrogen atom and an oxygen atom. A production process of an electrode catalyst for fuel cells is provided which includes a fluorination step of bringing a catalyst body into contact with fluorine, the catalyst body having an atom of at least one metal element selected from the group consisting of zinc, titanium, niobium, zirconium, aluminum, chromium, manganese, iron, cobalt, nickel, copper, strontium, yttrium, tin, tungsten, cerium, samarium and lanthanum, a carbon atom, a nitrogen atom and an oxygen atom.

Abstract: The present invention relates to a method of preparing catalysts based on molybdenum sulphide, with an alkaline promoter incorporated, said catalysts being employed in the production of alcohols, especially ethanol, from synthesis gas. The method involves reaction of molybdenum hexacarbonyl (Mo(CO)6) with sulphur, so as to generate molybdenum sulphide, in which an alkaline promoter is then incorporated, so as to obtain a solid catalyst for application in processes of production of alcohols from synthesis gas, selective for ethanol.

Abstract: Provided are a catalyst for hydrolysis and use of a titanium dioxide-based composition which are capable of removing COS and HCN simultaneously at high degradation percentages. The catalyst for hydrolysis is a catalyst for hydrolysis of carbonyl sulfide and hydrogen cyanide, having at least: an active component containing, as a main component, at least one metal selected from the group consisting of barium, nickel, ruthenium, cobalt, and molybdenum; and a titanium dioxide-based support supporting the active component.

Abstract: A method of preparation of metal-chalcogen-nitrogen-carbon (M-Ch-N—C) catalytic material utilizing a sacrificial support approach and using inexpensive and readily available precursors is described. Furthermore, the catalytic materials synthesized using the disclosed methods include multiple types of active sites.

Abstract: A catalyst for the treatment of exhaust gas emissions is disclosed. The catalyst can comprise ceria-alumina particles having a ceria phase present in a weight percent of the composite in the range of about 20% to about 80% on an oxide basis, an alkaline earth metal component supported on the ceria-alumina particles, wherein the CeO2 is present in the form of crystallites that are hydrothermally stable and have an average crystallite size less than 160 ? after aging at 950° C. for 5 hours in 2% O2 and 10% steam in N2.

Abstract: An improved composition capable of forming a translucent coating on a construction material surface comprising at least: a) photocatalytic titanium dioxide particles having at least a de-NOx activity; b) a silicon based-material in which said particles are dispersed, wherein said silicon based material includes at least one polysiloxane; and c) particles having a de-HNO3 activity selected from calcium carbonate, magnesium carbonate and mixtures thereof.

Abstract: The present invention concerns an oxygen reduction catalyst comprising composite particles in which primary particles of a titanium compound is dispersed into a carbon structure, wherein the composite particles have titanium, carbon, nitrogen and oxygen as constituent elements, and with regard to a ratio of number of atoms of each of the elements when titanium is taken as 1, a ratio of carbon is larger than 2 and 5 or less, a ratio of nitrogen is larger than 0 and 1 or less, and a ratio of oxygen is 1 or more and 3 or less, and an intensity ratio (D/G ratio) of D band peak intensity to G band peak intensity in a Raman spectrum is in the range of 0.4 to 1.0. The oxygen reduction catalyst according to the present invention has satisfactory initial performance and excellent start-stop durability.

Abstract: The present invention provides a catalyst which is not corroded in an acidic electrolyte or at a high potential, is excellent in durability and has high oxygen reduction ability. The catalyst of the present invention is characterized by including a niobium oxycarbonitride. The catalyst of the invention is also characterized by including a niobium oxycarbonitride represented by the composition formula NbCxNyOz, wherein x, y and z represent a ratio of the numbers of atoms and are numbers satisfying the conditions of 0.01?x?2, 0.01?y?2, 0.01?z?3 and x+y+z?5.

Abstract: An optimized catalyst system is disclosed for the pyrolysis of solid biomass material. The catalyst system is also suitable in upgrading reactions for biocrude. The system includes a carbonate species on a substantially inert support. The carbonate species can be an inorganic carbonate and/or an inorganic hydrogencarbonate.

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: The present invention discloses a process for producing a nano calcium carbonate slurry from a feedstock of waste gypsum, wherein: an aqueous gypsum slurry of the feedstock is mixed with ammonia water by stirring; with CO2 injected in the slurry is under continuous stirring until the calcium sulfate in the waste gypsum is completely carbonated into nano calcium carbonate; after filtration, the filter cake is dispersed in water to obtain the nano calcium carbonate slurry. This process is easy to operate and to obtain a low-cost and a lower decomposition temperature of calcium carbonate. The present invention also discloses a nano calcium carbonate slurry and its application in preparation of a CaO-based carbon dioxide adsorbent and complex catalyst used for a reactive sorption enhanced reforming process for hydrogen production from methane.

Abstract: A method of making ceramic membranes, and the ceramic membranes so formed, comprising combining a ceramic precursor with an organic or inorganic comonomer, forming the combination as a thin film on a substrate, photopolymerizing the thin film, and pyrolyzing the photopolymerized thin film.

Abstract: It is an object of the present invention to provide an oxygen reducing catalyst having high catalytic activity and high durability using a transition metal (such as titanium); and a method for producing a fuel cell electrode catalyst using the oxygen reducing catalyst. The present invention provides the oxygen reduction catalyst including titanium, carbon, nitrogen, and oxygen as constituent elements at a specific ratio, wherein in XRD measurement using a Cu—K? ray, peaks are each present in at least regions A and B among regions A to D which occupy 2? ranges of 42° to 43°, B: 36.5° to 37°, 25° to 26°, and 27° to 28°, respectively; and each of maximum peak intensities IA, IB, IC, and ID in the regions A to D satisfies both relationships of IA>IB and 0.3?(IA/(IA+IC+ID))?1.

Abstract: A supported catalyst useful in processes for chemically refining hydrocarbon feedstocks, the catalyst comprising a metal from Group 6, a metal from Group 8, and optionally phosphorous, wherein the carrier or support, comprises porous alumina comprising: (a) equal to or greater than about 78% to about 95% of TPV in pores having a diameter of less than about 200 Angstroms (A); (b) greater than about 2% to less than about 19% of the TPV in pores having a diameter of about 200 to less than about 1000 A; (c) equal to or greater than 3% to less than 12% of the TPV in pores having a diameter equal to or greater than about 1000 A.

Abstract: A system and method for splitting water to produce hydrogen and oxygen employing sunlight energy are disclosed. Hydrogen and oxygen may then be stored for later use as fuels. The system and method use inorganic capping agents that cap the surface of semiconductor nanocrystals to form photocatalytic capped colloidal nanocrystals, which may be deposited on a substrate and treated to form a photoactive material. The photoactive material may be employed in the system to harvest sunlight and produce energy necessary for water splitting. The system may also include elements necessary to collect, transfer and store hydrogen and oxygen, for subsequent transformation into electrical energy.

Abstract: A process for producing an oxygen reducing catalyst including a step of heat-treating, in a non-oxidizing atmosphere, a catalyst precursor including a compound (i) supplying a carbon element and a nitrogen element by heating in a non-oxidizing atmosphere, and a compound (ii) containing at least one element of iron and cobalt. Also disclosed is an oxygen reducing catalyst, a fuel cell catalyst layer including the oxygen reducing catalyst, an electrode including the fuel cell catalyst layer, a membrane-electrode assembly including the electrode and a fuel cell including the membrane-electrode assembly.

Abstract: The present invention relates to petrochemistry, gas chemistry, coal chemistry, particularly the invention relates to a catalyst for synthesis of hydrocarbons from CO and H2 and a preparation method thereof. The catalyst is pelletized and comprises at least Raney cobalt as active component in an amount of 1-40% by weight based on the total weight of the catalyst, metallic aluminium in an amount of 25-94% by weight based on the total weight of the catalyst and a binder in an amount of 5-30% by weight based on the total weight of the catalyst. The present invention provides the catalyst stability to overheating and high productivity of hydrocarbons C5-C100 for synthesis of hydrocarbons from CO and H2.

Abstract: An ionic liquid functionalized reduced graphite oxide (IL-RGO)/TiO2 nanocomposite was synthesized and used to reduce CO2 to a hydrocarbon in the presence of H2O vapor.

Abstract: Surface treatment agent with high photocatalytic and sanitary effects based on TiO2 nanoparticles comprising 10 to 500 g of TiO2nanoparticles per 1 liter of water, and binding ingredient A, which is an inorganic binder selected from the group comprising ZnO, MgO, CaO, Ca(OH)2, Mg(OH)2, CaCO3, MgCO3, Na2CO3, K2CO3 in the amount of 0.1 to 10% by weight related to the N weight of TiO2. Agent for treatment of surfaces for application on surfaces, which comprise a minimum of 50% of substances selected from the group formed by CaCO3, MgCO3 ZnO, MgO, CaO, Ca(OH)2, Mg(OH)2 or their mixtures, where the agent contains 10 to 500 g of TiO2 nanoparticles per 1 liter of water, and optionally contains a minimum of 0.1 wt % H2CO3 related to the weight of TiO2.

Abstract: [Problem] To provide a catalyst which has high oxygen reduction activity, also has excellent durability, and is inexpensive and excellent in electric power generation cost as compared with noble metal catalysts such as platinum. [Solution to problem] A catalyst for a polymer electrolyte fuel cell, including a graphitized carbon powder and a niobium oxycarbonitride or a titanium oxycarbonitride as an active substance, and a polymer electrolyte fuel cell using the catalyst.

Abstract: A fuel cell electrode catalyst which includes, at least, M1 that is at least one element selected from 3 to 7 group transition metal elements; M2 that is at least one element selected from iron group elements; M3 that is at least one element selected from 13 group elements; carbon; nitrogen; and oxygen, as constitutional elements, wherein when the atomic ratios of the elements (M1:M2:M3:carbon:nitrogen:oxygen) are represented by a:b:c:x:y:z, 0<a<1, 0<b?0.5, 0<c<1, 0<x?6, 0<y?2, 0<z?3 and a+b+c=1, and BET specific surface area is 100 m2/g or more.

Abstract: Catalytic forms and formulations are provided. The catalytic forms and formulations are useful in a variety of catalytic reactions, for example, the oxidative coupling of methane. Related methods for use and manufacture of the same are also disclosed.

Abstract: The invention describes the preparation of electrocatalysts, both anodic (aimed at the oxidation of the fuel) and cathodic (aimed at the reduction of the oxygen), based on mono- and plurimetallic carbon nitrides to be used in PEFC (Polymer electrolyte membrane fuel cells), DMFC (Direct methanol fuel cells) and H2 electrogenerators. The target of the invention is to obtain materials featuring a controlled metal composition based on carbon nitride clusters or on carbon nitride clusters supported on oxide-based ceramic materials. The preparation protocol consists of three steps. In the first the precursor is obtained through reactions of the type: a) sol-gel; b) gel-plastic; c) coagulation-flocculation-precipitation.

Abstract: The present invention relates to a method for producing esters from triglycerides by using solid heterogeneous catalysts comprised of calcined calcium carbonate, particularly for obtaining biodiesel.

Abstract: A method of making a metal oxide nanoparticle comprising contacting an aqueous solution of a metal salt with an oxidant. The method is safe, environmentally benign, and uses readily available precursors. The size of the nanoparticles, which can be as small as 1 nm or smaller, can be controlled by selecting appropriate conditions. The method is compatible with biologically derived scaffolds, such as virus particles chosen to bind a desired material. The resulting nanoparticles can be porous and provide advantageous properties as a catalyst.

Abstract: Catalysts of the invention are not corroded in acidic electrolytes or at high potential and have excellent durability and high oxygen reducing ability. A catalyst includes a metal oxycarbonitride containing niobium and at least one metal M selected from the group consisting of tin, indium, platinum, tantalum, zirconium, copper, iron, tungsten, chromium, molybdenum, hafnium, titanium, vanadium, cobalt, manganese, cerium, mercury, plutonium, gold, silver, iridium, palladium, yttrium, ruthenium, lanthanum, cerium, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, lutetium and nickel. A process for making the catalyst involves a heat treatment.

Abstract: A process for conversion of conventional sand granules (or other particulates) to a ‘core-shell’ adsorbent granules in which GO (or GO-f) coating imparts nano structural features on the surface of the sand granules (or other particulates). Such materials are useful in a variety of engineering applications such as water purification, catalysis, capacitors, proppants, casting, and magnetic shielding.

Abstract: A metal compound catalyst is formed by vaporizing a quantity of catalyst material and a quantity of carrier thereby forming a vapor cloud, exposing the vapor cloud to a co-reactant and quenching the vapor cloud. The nanoparticles are impregnated onto supports. The supports are able to be used in existing heterogeneous catalysis systems. A system for forming metal compound catalysts comprises means for vaporizing a quantity of catalyst material and a quantity of carrier, quenching the resulting vapor cloud, forming precipitate nanoparticles comprising a portion of catalyst material and a portion of carrier, and subjecting the nanoparticles to a co-reactant. The system further comprises means for impregnating the of supports with the nanoparticles.

Abstract: The invention relates to a method for producing micro-nano combined active systems in which nanoparticles of a first component are bonded to microparticles of a second component, comprising the following steps: (a) producing a low-ligand colloidal suspension containing nanoparticles of the first component, (b) adding microparticles to the colloidal suspension containing the nanoparticles or adding the colloidal suspension containing the nanoparticles to a dispersion containing the microparticles and intensively mixing so that the nanoparticles adsorb onto the microparticles, (c) separating the microparticles and the nanoparticles bonded thereto from the liquid and drying the microparticles and the nanoparticles bonded thereto.