Abstract: An improved process for converting an oil suspension of nanoparticles (NPs) into a water suspension of NPs, wherein water and surfactant plus salt is used instead of merely water and surfactant, leading to greatly improved NP aqueous suspensions.

Abstract: A method is described for lowering the nitrate content in a cobalt catalyst precursor formed by impregnating a catalyst support with cobalt nitrate, comprising calcining the impregnated support in air to effect partial denitrification and subsequently heating the calcined impregnated support to a temperature below 250° C. in the presence of a gas mixture comprising 0.1-10% hydrogen by volume in an inert gas.

Abstract: The invention relates to a multi-layer catalyst made from niobium for the catalytic conversion of hydrocarbons, comprising a) a support component made from a doped or undoped oxide or hydroxide of an element of the V sub-group of the periodic table, or mixtures thereof, b) a layer of a promoter compound, selected from oxygen, sulphur or phosphorus compounds of an element of the VI, VII and VIII sub-group or a phosphoxy compound and mixtures thereof and c) a layer comprising a compound of platinum metal. The invention further relates to a method for production of the catalyst and the use thereof.

Abstract: The present invention pertains to combustion catalysts, including processes for achieving increased thermal output from combustion processes, processes for improved combustion in boilers and furnaces, processes for reducing the emission of undesirable pollutants, and processes for increasing the combustion of carbon.

Abstract: An embodiment relates to a photocatalytic composite material comprising (a) a first component that generates a photoexcited electron and has at least a certain minimum bandgap to absorb visible light and a structure that substantially prevents the recombination of the photoexcited electron and a hole; (b) a second component that adsorbs/absorbs an oxide of carbon; and (c) a third component that splits the oxide of carbon into carbon and oxygen using the photoexcited electron.

Abstract: A catalyst comprising a dehydrogenation catalyst and a water gas shift co-catalyst can be used for the dehydrogenation of alkylaromatic hydrocarbons to alkenylaromatic hydrocarbons. For instance, the catalyst can be used for the dehydrogenation of ethylbenzene to styrene. The catalyst can include an iron compound, a potassium compound, and a cerium compound.

Abstract: An improved carrier useful for preparing a catalyst having excellent catalytic performance when used in the production of alkylene oxide, such as ethylene oxide. The carrier is obtained by a) impregnating a preformed alpha-alumina carrier with at least one modifier selected from among alkali metal silicates and alkaline earth metal silicates, b) drying the impregnated carrier; and c) calcining dried carrier. The carrier may optionally be washed, prior to being impregnated by conventional catalytic material and/or promoter material.

Abstract: The invention relates to a supported catalyst based on palladium-?-alumina, which is characterized in that the catalyst support material contains 1 to 1000 ppm by mass of sodium oxide and has a specific pore volume of 0.4 to 0.9 ml/g and a BET surface area of 150 to 350 m2/g. The invention further relates to a process for hydrogenating polyunsaturated ethers with hydrogen to the corresponding saturated ethers, in which the catalyst used is such a catalyst.

Abstract: A particulate desulphurisation material includes one or more nickel compounds, a zinc oxide support material, and one or more alkali metal compounds wherein the nickel content of the material is in the range 0.3 to 10% by weight and the alkali metal content of the material is in the range 0.2 to 10% by weight. A method of making the desulphurisation material includes the steps: (i) contacting a nickel compound with a particulate zinc support material and an alkali metal compound to form an alkali-doped composition, (ii) shaping the alkali-doped composition, and (iii) drying, calcining, and optionally reducing the resulting material. The desulphurisation material may be used to desulphurise hydrocarbon gas streams with reduced levels of hydrocarbon hydrogenolysis.

Abstract: A method of producing a Fischer-Tropsch catalyst by preparing a nitrate solution, wherein preparing comprises forming at least one metal slurry and combining the at least one metal slurry with a nitric acid solution; combining the nitrate solution with a basic solution to form a precipitate; promoting the precipitate to form a promoted mixture, wherein promoting comprises combining the precipitate with (a) silicic acid and one or more selected from the group consisting of non-crystalline silicas, crystalline silicas, and sources of kaolin or (b) at least one selected from non-crystalline silicas and sources of kaolin, in the absence of silicic acid; and spray drying the promoted mixture to produce catalyst having a desired particle size. Catalyst produced by the disclosed method is also described.

Abstract: An improved process to produce high surface area nanoparticle vanadium phosphorus oxide catalysts comprises the steps of reducing vanadium-containing compounds in an alcohol solution selected from the group consisting of isobutanol and benzyl alcohol and any combination derives thereof under reflux for 4 to 6 hours to form a suspended mixture; reacting dopants and phosphorus-containing compounds to the suspended mixture under reflux for 30 minutes to 3 hours to form precursors of the vanadium phosphorus oxide catalysts; drying the formed precursors; and calcining the dried precursors in a flow of gaseous n-butane/air mixture at 400 to 460° C. to form activated vanadium phosphorus oxide catalysts.

Abstract: A photocatalyst film of which at least one main surface contains photo-semiconductor particles; said main surface being a surface that becomes hydrophilic by irradiation with light, wherein the hydrophilization speed thereof when it is irradiated with light having a half-value width of 15 nm or less after kept in a dark place is less than 2 (l/deg/min/105) in an irradiated-light wavelength region of 370 nm or more and is 2 (l/deg/min/105) or more at least partly in an irradiated-light wavelength region of 300 to 360 nm.

Abstract: A particulate unsupported superacid catalyst for use in fluid catalytic cracking is provided comprising doped silica which has been doped with from about 1 to about 99 wt %, based on the weight of the catalyst composition, of at least one inorganic oxide dopant selected from the group consisting of rare earth metal oxides, alkaline earth metal oxides, zinc oxide, magnesium oxide, manganese oxide, yttrium oxide, niobium oxide, zirconium oxide and titanium oxide, and wherein the doped silica has been anion-modified by an anion selected from the group consisting of phosphate, tungstate, and sulphate.

Abstract: The present invention relates to an esterification catalyst composition that includes a zirconium compound and a method for producing an ester compound, which includes the steps of esterifying alcohol and carboxylic acid compounds by using the same, and it may be applied to a mass synthesis process.

Abstract: A catalyst and a method for selective hydrogenation of acetylene and dienes in light olefin feedstreams are provided. The catalyst retains higher activity and selectivity after regeneration than conventional selective hydrogenation catalysts. The catalyst contains a first component and a second component supported on an inorganic support. The inorganic support contains at least one salt or oxide of zirconium, a lanthanide, or an alkaline earth.

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 process utilising the gases carbon monoxide, carbon dioxide and hydrogen to produce alcohols directly, comprises the steps of bringing a fluid mixture comprising carbon monoxide, carbon dioxide and hydrogen into contact with the surfaces of a supported tubular porous catalyst membrane having a range of pore sizes including micropores, mesopores and macropores, controlling the temperature of the said catalyst membrane, maintaining a pressure over said catalyst membrane of from 88 to 600 kPa, and recovering alcohol containing product formed by contact of the fluid mixture with said catalyst membrane.

Abstract: A process for producing geometric shaped catalyst bodies K whose active material is a multielement oxide which comprises the element Mo, the elements Bi and/or V and one or more of the elements Co, Ni, Fe, Cu and alkali metals, in which sources of the different elements are used to obtain a finely divided mixture which is coarsened to a powder by press agglomeration, the coarsened powder is used to form, by press agglomeration, shaped bodies V which are separated into undamaged shaped bodies V+ and into damaged shaped bodies V?, the undamaged shaped bodies V+ are converted by thermal treatment to the shaped catalyst bodies K, and the damaged shaped bodies V? are comminuted and recycled into the obtaining of the finely divided mixture.

Abstract: A NOx storage material comprises a support, a potassium salt impregnated on the support, the potassium impregnated on the support is promoted with a platinum group metal, and wherein the NOx storage material has an electrical property which changes based on the amount of NOx loading on the NOx storage material. An apparatus for direct NOx measurement includes a sensor coated with the NOx storage material. A method of determining NOx flux in a NOx containing gas comprises exposing the gas to the apparatus and converting a signal developed by the apparatus to a signal representative of the NOx flux.

Abstract: Aircraft catalysts, systems, and methods are disclosed. In one or more embodiments, the catalysts comprise a substrate, at least a first washcoat layer on the substrate comprising a refractory metal oxide support having a catalytic metal component dispersed on the refractory metal oxide support, and an overcoat washcoat layer on the first layer comprising a manganese component. Catalysts prepared in accordance with embodiments of the invention exhibit improved life when used in aircraft.

Abstract: Bimetallic, supported catalysts for production of 1-hexene from ethylene are manufactured by impregnating a porous, solid support material with at least one catalytic chromium compound and at least one catalytic tantalum compound. The bimetallic, supported catalysts have high catalytic turnover, high selectivity for 1-hexene production, a low tendency for metals to leach from the catalysts during manufacturing and use compared to catalysts manufactured using known techniques. Moreover, the catalysts can be reused in multiple synthesis runs. High turnover, high selectivity, and reusability improve yields and reduce the costs associated with producing 1-hexene from ethylene, while the absence of metal leaching reduces the potential environmental impacts of using toxic metal catalysts (e.g., chromium).

Abstract: A catalyst having at least 5 weight percent of an alumina compound useful for the dehydrogenation of alkylaromatic hydrocarbons to alkenylaromatic hydrocarbons and methods of use are disclosed.

Abstract: A process for producing a ringlike oxidic shaped body by mechanically compacting a pulverulent aggregate introduced into the fill chamber of a die, wherein the outer face of the resulting compact corresponds to that of a frustocone.

Abstract: A method of producing a catalyst precursor comprising iron phases by co-feeding a ferrous nitrate solution and a precipitation agent into a ferric nitrate solution to produce a precipitation solution having a desired ferrous:ferric nitrate ratio and from which catalyst precursor precipitates; co-feeding a ferric nitrate solution and a precipitation agent into a ferrous nitrate solution to produce a precipitation solution having a desired ferrous:ferric nitrate ratio and from which catalyst precursor precipitates; or precipitating a ferrous precipitate from a ferrous nitrate solution by contacting the ferrous nitrate solution with a first precipitation agent; precipitating a ferric precipitate from ferric nitrate solution by contacting the ferric nitrate solution with a second precipitation agent and combining the ferrous and ferric precipitates to form the catalyst precursor, wherein the ratio of ferrous:ferric precipitates is a desired ratio.

Abstract: A method comprising contacting a support with a chromium-containing compound and a tin-containing compound to produce a catalyst precursor, and activating the catalyst precursor in a temperature range of from about 400° C. to about 700° C. to produce a polymerization catalyst. A method comprising contacting a support with a chromium-containing compound and a tin-containing compound to produce a catalyst precursor, activating the catalyst precursor in a temperature range of from about 400° C. to about 700° C. to produce a polymerization catalyst, and contacting the polymerization catalyst with ethylene in a reaction zone under suitable reaction conditions to form polyethylene wherein the molecular weight distribution of the polyethylene is broadened.

Abstract: To provide a production process of an oxidation catalyst apparatus for purifying an exhaust gas which enables to oxidize and purify particulate matter in the exhaust gas of an internal combustion engine at a lower temperature. The production process of the oxidation catalyst apparatus 1 for purifying an exhaust gas comprises a step of burning a plurality of metal compounds to obtain a burnt product, a step of mixing and grinding the obtained burnt product with water and a binder which is a sol comprising zirconia to prepare a slurry, a step of applying the slurry to a porous filter base material 2, and a step of burning the porous filter base material 2 to form a porous catalyst layer 3 supported on the porous filter base material 2. The porous catalyst layer 3 has a thickness in a range of 10 to 150 ?m and fine pores having a diameter in a range of 0.01 to 5 ?m, the total porosity of and the porous filter base material 2 and the porous catalyst layer 3 have a porosity of 35 to 70% as a whole.

Abstract: A catalyst which comprises a carrier and silver deposited on the carrier, which carrier has a surface area of at least 1.3 m2/g, a median pore diameter of more than 0.8 ?m, and a pore size distribution wherein at least 80% of the total pore volume is contained in pores with diameters in the range of from 0.1 to 10 ?m and at least 80% of the pore volume contained in the pores with diameters in the range of from 0.1 to 10 ?m is contained in pores with diameters in the range of from 0.

Abstract: The invention relates to a catalyst with large surface area structure, in particular for steam-reforming catalysts, which is characterised in that the large surface area structure is formed of a large number of round or parallel penetrating holes of polygonal cross-section, wherein the catalyst carrier is prepared in the injection moulding process, coated with a washcoat and then impregnated with the active component. The catalyst carrier includes at least one sinterable material and has a lateral pressure resistance of at least 700 N. The invention further relates to a process for the preparation of such catalysts and the use thereof in a reactor.

Abstract: A process for producing a supported Fischer-Tropsch catalyst includes treating, in an activation stage (12), a particulate pre-reduction cobalt nitrate-based supported Fischer-Tropsch synthesis catalyst precursor containing reducible cobalt oxides, with hydrogen as a reducing gas in order to reduce the cobalt oxides over a period of time to Co, with ammonia and water being formed, the reduction including a time period when predominantly CoO is reduced to Co. Unreacted hydrogen is withdrawn (20), which thus includes water and treated to lower its dewpoint (14). At least a portion of the withdrawn unreacted hydrogen is returned to the activation stage (12) as recycle hydrogen (26). An ammonia concentration is maintained in the activation stage (12), at least during the time when predominantly CoO is reduced to Co, of less than 250 volume parts per million (‘vppm’).

Abstract: A method of strengthening a precipitated unsupported iron catalyst by: preparing a precipitated unsupported iron catalyst containing copper and potassium; adding a solution comprising a structural promoter to the previously prepared catalyst; drying the mixture; and calcining the dried catalyst. A method for preparing an iron catalyst, the method comprising: precipitating a catalyst precursor comprising iron phases selected from hydroxides, oxides, and carbonates; adding a promoter to the catalyst precursor to yield a promoted precursor; drying the promoted precursor to yield dried catalyst; and calcining the dried catalyst, wherein the catalyst further comprises copper and potassium. A method of preparing a strengthened precipitated iron catalyst comprising: co-precipitating iron, copper, magnesium, and aluminum; washing the precipitate; alkalizing the precipitate; and drying the precipitate to yield a dried catalyst precursor.

Abstract: A catalyst for use in the Fischer-Tropsch process, and a method to prepare the catalyst is disclosed. The catalyst of the present invention has a higher surface area, more uniform metal distribution, and smaller metal crystallite size than Fischer-Tropsch catalysts of the prior art.

Abstract: A catalyst on an oxidic support and processes for selectively hydrogenating unsaturated compounds in hydrocarbon streams comprising them using these catalysts are described.

Abstract: An object of the present invention is to provide a catalyst composition containing a perovskite-type composite oxide which exhibits a satisfactory catalytic performance over a long time even in a high temperature atmosphere and has a stable quality in which Rh and/or Pt dissolves to form a solid solution at a high rate. To achieve the object described above, in the present invention the catalyst composition is prepared to comprise an Rh-containing perovskite-type composite oxide represented by the following general formula (I) and/or a Pt-containing perovskite-type composite oxide represented by the following general formula (II) and a thermostable oxide optionally containing a noble metal.

Abstract: To provide an SO3 reduction catalyst for purifying an exhaust gas capable of efficiently reducing the amount of SO3 that is present in a combustion exhaust gas and is a starting substance of S-containing substances such as acid ammonium sulfate causing deterioration of performance of the catalyst or corrosion of apparatuses disposed downstream of the catalyst, or capable of controlling the generation of SO3 in the catalyst itself; a preparation process of the catalyst; and an exhaust gas purifying method using the catalyst. In the catalyst for purifying a combustion exhaust gas containing nitrogen oxides, 50 wt. % or greater of the amount of Ru and/or Ir to be supported is adjusted to fall within a depth of 150 ?m from the surface layer of a substrate; and the catalyst is prepared by immersing the substrate in a metal colloid solution of Ru and/or Ir to be supported or an aqueous solution containing at least one compound selected from compounds of Ru and/or Ir to be supported.

Abstract: A catalyst composition comprising a support having a surface area of at least 500 m2/kg, and deposited on the support: silver metal, a metal or component comprising rhenium, tungsten, molybdenum or a nitrate- or nitrite-forming compound, and a Group IA metal or component comprising a Group IA metal having an atomic number of at least 37, and in addition potassium, wherein the value of the expression (QK/R)+QHIA is in the range of from 1.5 to 30 mmole/kg, wherein QHIA and QK represent the quantities in mmole/kg of the Group IA metal having an atomic number of at least 37 and potassium, respectively, present in the catalyst composition, the ratio of QHIA to QK is at least 1:1, the value of QK is at least 0.01 mmole/kg, and R is a dimensionless number in the range of from 1.5 to 5, the units mmole/kg being relative to the weight of the catalyst composition.

Abstract: Catalyst for the polymerization and/or copolymerization of olefins which has a chromium content of from 0.01 to 5% by weight, based on the element in the finished catalyst, is supported on a finely divided inorganic support and is obtainable by concluding calcination at temperatures of from 350 to 1050° C. and has a zinc content of from 0.01 to 10% by weight, based on the element in the finished catalyst.

Abstract: A process and catalyst for the liquid phase selective hydrogenation of alkynes to alkenes with high selectivity to alkenes relative to alkanes, high alkyne conversion, and sustained catalytic activity comprising a reactant comprising an alkyne and a non-hydrocarbon solvent/absorbent, contacting the reactant stream with a hydrogen-containing stream in the presence of a supported, promoted, Group VIII catalyst, removing the solvent/absorbent, and recovering the alkene product.

Abstract: A catalyst and process is disclosed to selectively upgrade a paraffinic feedstock to obtain an isoparaffin-rich product for blending into gasoline. The catalyst comprises a support of a tungstated oxide or hydroxide of a Group IVB (IUPAC 4) metal, a phosphorus component, and at least one platinum-group metal component which is preferably platinum. The catalyst has a structure other than a hetropoly anion structure.

Abstract: A catalyst and a method for selective hydrogenation of acetylene and dienes in light olefin feedstreams are provided. The catalyst retains higher activity and selectivity after regeneration than conventional selective hydrogenation catalysts. The catalyst contains a first component and a second component supported on an inorganic support. The inorganic support contains at least one salt or oxide of zirconium, a lanthanide, or an alkaline earth.

Abstract: A method is described for lowering the nitrate content in a cobalt catalyst precursor formed by impregnating a catalyst support with cobalt nitrate, comprising calcining the impregnated support in air to effect partial denitrification and subsequently heating the calcined impregnated support to a temperature below 250° C. in the presence of a gas mixture comprising 0.1-10% hydrogen by volume in an inert gas.

Abstract: A method for the preparation of a catalyst or catalyst precursor comprising: (a) admixing a carrier material, a homogeneous crystalline solid solution of a cobalt compound and one or more d-metal compounds and/or one or more co-catalysts or precursors thereof, and optionally a liquid; (b) forming the mixture of step (a); and (c) optionally drying and/or calcining the product of step (b).

Abstract: A process for treating a carrier, or a precursor thereof, to at least partly remove impurities comprising contacting the carrier, or the precursor thereof, with a treatment solution comprising a salt; a process for preparing a catalyst; the catalyst; a process for preparing an olefin oxide by reacting an olefin with oxygen in the presence of the catalyst; and a process for preparing a 1,2-diol, a 1,2-diol ether or an alkanolamine.

Abstract: The present invention relates to a catalyst used for producing dimethylether, a method of producing the same, and a method of producing dimethylether using the same. More particularly, the present invention relates to a catalyst used for producing dimethylether comprising a methanol synthesis catalyst produced by adding one or more promoters to a main catalyst comprised of a Cu—Zn—Al metal component and a dehydration catalyst formed by mixing Aluminum Phosphate (AlPO4) with gamma alumina, a method of producing the same, and a method of producing dimethylether using the same, wherein a ratio of the main catalyst to the promoter in the methanol synthesis catalyst is in a range of 99/1 to 95/5, and a mixing ratio of the methanol synthesis catalyst to the dehydration catalyst is in a range of 60/40 to 70/30.

Abstract: A catalyst for the hydrogenation of C4-dicarboxylic acids and/or derivatives thereof, preferably maleic anhydride, in the gas phase comprises a) 20-94% by weight of copper oxide (CuO), preferably 40-92% by weight of CuO, in particular 60-90% by weight of CuO, and b) 0.005-5% by weight, preferably 0.01-3% by weight, in particular 0.05-2% by weight, palladium and/or a palladium compound (calculated as metallic palladium) and c) 2-79.995% by weight, preferably 5-59.99% by weight, in particular 8-39.95% by weight, of an oxidic support selected from the group consisting of the oxides of Al, Si, Zn, La, Ce, the elements of groups IIIA to VIIIA and of groups IA and IIA of the Periodic Table of the Elements.

Abstract: A catalyst for use in a Fischer-Tropsch synthesis reaction which comprises cobalt supported on alumina, in which: the catalyst average particle size is in the range 20 to 100 ?m; the specific surface area of the impregnated and calcined catalyst particles is greater than 80 m2/g; the average pore size of the impregnated and calcined catalyst is at least 90 ? (9 nm); and the pore volume of the impregnated and calcined catalyst is greater than 0.35 cm3g.

Abstract: An embodiment of the present invention comprises a ceramic catalyst comprising a porous ceramic/silica glass substrate having substantially interconnecting pores with an average pore size of approximately 2 micron or less and particles comprising one or more noble metals on the surface of the substantially interconnecting pores. The noble metal particles may be either amorphous and/or crystalline nano-particles. The noble metals preferably may comprise silver, gold, rhodium, and/or palladium. The average pore size may be approximately 1 micron or less, 0.5 microns or less, 0.3 microns or less, 0.2 microns or less, 100 nanometers or less, 50 nanometers or less, or between 50 nanometers and 150 nanometers. Other embodiments of the present invention are directed to methods of manufacturing the ceramic catalyst and novel glass compositions used to manufacture the ceramic catalyst and using the ceramic catalyst at temperatures above 200° C. to produce hydrogen gas and to store hydrogen gas.

Abstract: Processes for preparing a composition comprising (i) an acidic metal oxide containing substantially no zeolite, (ii) an alkali metal, alkaline earth metal, and mixtures thereof, and (iii) an oxygen storage component are disclosed. Preferably, the process comprise forming a single slurry of components (i)–(iii), spray drying and calcining to obtain metal oxide particles comprising components (i)–(iii). Preferably, the slurry comprise a base peptized acidic metal oxide containing slurry wherein the component (ii) is provided in the slurry as a metal of the base. Compositions prepared are impregnated with a noble metal to provide compositions useful to reduce gas phase reduced nitrogen species and NOx in an effluent off gas of a fluid catalytic cracking regenerator.

Abstract: A method of making an exhaust treatment catalyst includes dispersing a metal-based material in a first solvent to form a first slurry and allowing polymerization of the first slurry to occur. Polymerization of the first slurry may be quenched and the first slurry may be allowed to harden into a solid. This solid may be redistributed in a second solvent to form a second slurry. The second slurry may be loaded with a silver-based material, and a silver-loaded powder may be formed from the second slurry.

Abstract: Provided is a novel heteropolyacid catalyst useful for partial oxidation of methacrolein (MACR) to methacrylic acid (MAA), as represented by the following formula 1: PMoaAbBcCdDeEfOg??(1) wherein A, B, C, D, E, a, b, c, d, e, f, and g are as defined in the specification. Provided is also a method for producing the heteropolyacid catalyst. The heteropolyacid catalyst produced by the method exhibits excellent catalyst activity in terms of conversion rate, selectivity, and yield.

Abstract: A molten-salt type catalyst is adapted for purifying particulate materials, which are contained in an exhaust gas emitted from an internal combustion engine and contain carbon. It includes a solid support and a catalytic ingredient. The catalytic ingredient is loaded on the solid support, and includes at least one member selected from the group consisting of silver nitrate, alkali metal nitrate, alkaline-earth metal nitrate and rare-earth nitrate. The molten-type catalyst can efficiently burn and remove the particulate materials even in a low temperature range.