Abstract: The present invention is a method for manufacturing a high-performance composite active material of zinc oxide powder, which is a method for manufacturing a high-performance composite active zinc oxide material powder as an aid for an operation of shaping and vulcanization of rubber/plastic materials, generally carried out by mixing an alkali solution and a calcium compound, in combination with addition of a zinc salt to directly carry out a chemical reaction therewith through mixture so as to obtain a precipitation solution of a predetermined pH value, following a process of filtering to remove water to form an intermediate powder material, which is subjected to drying to form zinc oxide long crystal material exhibiting nanometer scale high performance composite activity, helping achieve a purpose of diversification of application of zinc oxide power in industry.

Abstract: A highly active quaternary mixed transition metal oxide material has been developed. The material may be sulfided to generate metal sulfides which are used as a catalyst in a conversion process such as hydroprocessing. The hydroprocessing may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

Abstract: The present invention provides an oxygen scavenger composition comprising a granule having: an ? layer containing a water retention agent, a swelling agent, a metal salt and water; a ? layer containing iron; and a ? layer containing a porous support, wherein the granule forms a layer structure in order of the ? layer, the ? layer and the ? layer from an inside to an outside of the granule.

Abstract: Provided is a method for producing an inorganic oxide in the form of a thin film, the method including a step of bringing a first liquid and a second liquid into contact with each other, the first liquid having an inorganic oxide precursor dissolved therein, the second liquid phase-separating from the first liquid and having a substance dissolved therein, the substance reacting with the inorganic oxide precursor of the first liquid to form an inorganic oxide derived from the inorganic oxide precursor. The segment size of the first liquid at the time of contact between the first and second liquids is 500 ?m or smaller.

Abstract: A mixed metal oxide catalyst includes NiMnO nanoparticles on a TiO2 nanoparticle support. The catalyst may be used to produce biodiesel from waste oils, such as used cooking oils, through a transesterification reaction. The process of producing biodiesel using waste oils using the mixed metal oxide catalyst eliminates a need for quenching, reduces issues related to saponification and glycerol recovery, and allows for easy recovery and reuse of the mixed metal oxide catalyst in an economical and environmentally friendly way.

Abstract: A method is described of producing a catalyst-containing composite oxygen ion membrane and a catalyst-containing composite oxygen ion membrane in which a porous fuel oxidation layer and a dense separation layer and optionally, a porous surface exchange layer are formed on a porous support from mixtures of (Ln1?xAx)wCr1?yByO3?? and a doped zirconia. Adding certain catalyst metals into the fuel oxidation layer not only enhances the initial oxygen flux, but also reduces the degradation rate of the oxygen flux over long-term operation. One of the possible reasons for the improved flux and stability is that the addition of the catalyst metal reduces the chemical reaction between the (Ln1?xAx)wCr1?yByO3?? and the zirconia phases during membrane fabrication and operation, as indicated by the X-ray diffraction results.

Abstract: A catalyst comprising: a titanium oxide having an anatase-type crystal structure, and having the vertices and the ridge lines, wherein in a single titanium oxide particle, a vertex density per unit surface area is 8.0×10?4 nm?2 or more, and a ridge line density per unit surface area is 5.0×10?2 nm or more, or a ridge line density per unit volume is 8.0×10?3 nm?2 or more. A complex comprising: a material having a porous structure; and said catalyst. A membrane electrode assembly comprising: an anode; cathode; and an electrolyte membrane, wherein the cathode carries said catalyst on at least a surface of the cathode.

Abstract: A particulate composition said composition comprises a metal carbonate and/or a metal bicarbonate and a compound of aluminium, characterised in that the weight ratio of metal carbonate plus metal bicarbonate compounds to said compound of aluminium is at least 3:1. The composition is useful for removing halogenated compounds from a hydrocarbon-containing process stream.

Abstract: A highly active quaternary mixed transition metal oxide material has been developed. The material may be sulfided to generate metal sulfides which are used as a catalyst in a conversion process such as hydroprocessing. The hydroprocessing may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

Abstract: The present invention relates to a method for producing potassium titanate, and the present invention provides a method for producing potassium titanate which uses anatase-phased titanium dioxide to simplify the process by a hydrothermal method, and thus may improve economical efficiency and productivity, and in which the reaction temperature, the reaction time and the molar ratio of a precursor may be controlled to produce a high-purity potassium titanate whisker having a nano size of an uniform shape.

Abstract: A method for producing an iron-containing filter material for water treatment includes the steps of reacting a trivalent iron compound and a base inside a vessel until the trivalent iron is completely neutralized, to obtain an iron hydroxide and a salt consisting of the anion of the trivalent iron compound and the cation of the base; feeding the iron hydroxide and the salt into ceramic membranes to wash the iron hydroxide from the salt in cross-flow; feeding the iron hydroxide suspension to a membrane filter press where part of the water is removed, to obtain a panel having a moisture content of less than 77% by weight; inserting the panel into containers; and positioning the containers inside a refrigeration chamber operating at atmospheric pressure and at temperatures less than 0° C. for a time between 24 and 240 hours.

Abstract: The copper oxide nanoparticles synthesized using Rhatany root extract involves preparing the Rhatany root extract by adding powdered Rhatany roots to boiling water, allowing the mixture to soak overnight, and removing any solid residue by filtering to obtain the aqueous extract. The copper oxide nanoparticles are prepared by mixing equal volumes of the aqueous Rhatany root extract and 0.1 M aqueous copper sulfate, heating the mixture at 80° C. for 40 minutes, and adding 1 M sodium hydroxide dropwise to the mixture to precipitate CuO. The precipitate is removed by centrifuge, washed with ethanol, dried, and calcined at 400° C. for 4 hours to obtain the copper oxide nanoparticles. The resulting nanoparticles proved effective in degrading wastewater dyes, showed anticancer activity against human cervical cancer by cell viability assay, and showed antibacterial activity against various strains of bacteria by agar diffusion.

Abstract: A method of synthesizing copper oxide nanoparticles includes preparing a liquid extract of Rumex vesicarius, dissolving copper salt in the liquid extract to provide a solution with copper nanoparticles, adding a base to the solution with copper nanoparticles to form a precipitate including copper oxide nanoparticles. Copper oxide nanoparticles prepared according to the method are effective photocatalysts for degrading organic dyes and antibacterial agents and exhibit anticancer activities.

Abstract: A unique crystalline mixed transition metal tungstate material has been developed material may be sulfided to generate metal sulfides which are used as a catalyst in a conversion process such as hydroprocessing. The hydroprocessing may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodesilication, hydrodearomatization, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

Abstract: A ceria-zirconia-based composite oxide oxygen storage material with a fast oxygen storage rate having an OSC ability enabling fast response to changes in exhaust gas which does not greatly fluctuate in composition, but varies at a fast rate near the stoichiometric air-fuel ratio, an exhaust gas purification catalyst, and a honeycomb structure for exhaust gas purification are provided. A ceria-zirconia-based composite oxide oxygen storage material, which oxygen storage material has a molar ratio of cerium and zirconium, by cerium/(cerium+zirconium), of 0.33 to 0.90, has an ion conductivity measured by an AC impedance method of 1×10?5S/cm or more at 400° C., and contains metal ions M of one or more types of rare earth elements selected from Sm3+, Eu3+, Pr3+, Gd3+, and Dy3+ with a coordination number of over 7.0 in an amount of 0.5 mol % to 15 mol % with respect to the total amount of cations.

Abstract: A three-way catalyst article, and its use in an exhaust system for internal combustion engines, is disclosed. The catalyst article for treating exhaust gas comprising: a substrate; and a single catalyst layer deposited directly on the substrate; wherein the single catalyst layer comprises a first platinum group metal (PGM) component, an oxygen storage component (OSC) material, and an inorganic oxide; and wherein the single catalyst layer has a total washcoat loading of less than 2.4 g/in3.

Abstract: A hydrated lime product exhibiting superior reactivity towards HCl and SO2 in air pollution control applications. Also disclosed is a method of providing highly reactive hydrated lime and the resultant lime hydrate where an initial lime feed comprising calcium and impurities is first ground to a particle-size distribution with relatively course particles. Smaller particles are then removed from this ground lime and the smaller particles are hydrated and flash dried to form a hydrated lime, which is then milled to a significantly smaller particle size than that of the relatively course particles. The resultant lime hydrate product has available CaOH of greater than 92%, a citric acid reactivity of less than 20 seconds, a BET surface area greater than 18, a D90 less than 10 ?m, a D50 less than 4 ?m, a D90/D50 less than 3, and a large pore volume of greater than 0.2 BJH.

Abstract: The present invention relates to a honeycomb structured body including a honeycomb fired body in which multiple through-holes are arranged longitudinally in parallel with one another with a partition wall therebetween, wherein the honeycomb fired body is an extrudate containing ceria-zirconia composite oxide particles, ?-alumina particles, ?-alumina, and ?-alumina fibers, and the honeycomb fired body has a porosity of 55 to 70%.

Abstract: Carbon nanoparticles are decorated with ultrafine hafnium promethium nanowires. Exemplary nanowires of hafnium promethium oxide (e.g., Hf0.7Pm0.3O2) have been fabricated. The carbon nanoparticles decorated with hafnium promethium nanowires may be used in reactions for reducing carbon dioxide to methanol, and have applications as a photocatalyst for energy applications.

Abstract: An oxygen evolution catalyst of the formula: Sr2MCoO5 where M=Al, Ga wherein M is bonded with four oxygen atoms to form a tetrahedron. The catalyst is operated at a potential of less than 1.58 volts vs. RHE at a current density of 50 ?A/cm2 for a pH of 7-13. The catalyst is operated at a potential of less than 1.55 volts vs. RHE at a current density of 50 ?A/cm2 and a pH of 13. The oxygen evolution catalyst of the formula: Sr2GaCoO5 wherein the catalyst is operated at a potential of less than 1.53 volts vs. RHE at a current density of 50 ?A/cm2 and a pH of 7. The oxygen evolution catalyst of formula: Sr2GaCoO5 wherein the catalyst maintains a current within 94% after 300 minutes at a potential of 1.645 volts vs. RHE wherein the current is greater than 1 milliamp and a pH of 7.