Disclosed are a catalyst for producing olefin and a preparation method thereof. The catalyst for producing olefin includes: a support including an alumina and a sub-support component; and a catalytic component comprising a metal component and an alkali metal impregnated on the support. The preparation method includes: providing a support comprising a sub-support component and an alumina; preparing pre-catalyst by dipping a metal component oxide in the support and calcining it; and dipping a metal component oxide and an alkali metal oxide in the pre-catalyst and calcining it.

A catalyst for producing unsaturated aldehyde and unsaturated carboxylic acid, wherein the cumulative pore volume (A) of pores having a pore diameter of 1 m or more and 100 m or less, in the catalyst, is 0.12 ml/g or more and 0.19 ml/g or less, and the ratio (A/B) of the cumulative pore volume (A) to the cumulative pore volume (B) of pores having a pore diameter of 1 m or more and 100 m or less, in a pulverized product not passing through a Tyler 6 mesh, in a pulverized product obtained by pulverization of the catalyst under a particular condition is 0.30 or more and 0.87 or less.

In one aspect, catalyst modules are described herein comprises structural catalyst bodies having cross-sectional flow channel geometries and surface features for enhanced catalytic activity. In some embodiments, the catalyst modules and associated structural catalyst bodies are suitable for use in high particulate matter environments. Briefly, a catalyst module comprises a framework and a plurality of structural catalyst bodies positioned in the framework, a structural catalyst body comprising an outer peripheral wall and a plurality of inner partition walls forming individual flow channels of rectangular cross-section, the outer peripheral wall resistant to localized flexural failures induced by material between adjacent structural catalyst bodies of the module.

A composite catalyst includes a carrier and noble metal particles supported by the carrier, wherein the carrier is a nitrogen-doped porous carbon composite material having a plurality of passages. The nitrogen-doped porous carbon composite material can include a nitrogen-doped porous carbon material and a plurality of metal oxide particles. The plurality of metal oxide particles can be uniformly distributed in the nitrogen-doped porous carbon material. The plurality of metal oxide particles can be partially exposed through the plurality of passages. The noble metal particles can be tightly combined with the exposed metal oxide particles to achieve recombination. And the noble metal particles can be at least one of Pd metal particles, Pt metal particles, Ru metal particles, Rh metal particles, Ir metal particles, Au metal particles, or a combination thereof.

A nanocomposite composition for oxidative desulfurization of liquid hydrocarbon fuels, is disclosed. The nanocomposite composition comprises an amorphous mesoporous titania-silica (TiO.sub.2SiO.sub.2) nanocomposite oxidative desulfurization (ODS) catalyst-adsorbent, including, a chelating agent, an alcohol, an alkoxides precursor of silica and titania, water, an organic polymer and a textural agent. The nanocomposite ODS catalyst-adsorbent is prepared with the aid of polyethylene glycol (PEG) as directing agent and citric acid (CA) as chelating agent. The PEG increases the specific surface area and average pore diameter of ODS catalyst-adsorbent, which facilitates the diffusion of bulky sulfur compounds into porosities of catalyst and adsorption of oxidized sulfur compounds on the catalyst surface. The citric acid controls the hydrolysis and condensation of titanium precursor, which improves ODS performance of catalyst-adsorbent. Further, the prepared ODS catalyst-adsorbent is a dual function material capable of catalyzing the oxidation sulfur compounds and their removal to an ultra-low level in hydrocarbon fuel.

The catalyst for ammoxidation of the present invention contains a catalyst particle containing molybdenum, bismuth and iron, and has a ratio of hollow particles of 23% or less. Furthermore, a method for producing the catalyst for ammoxidation includes a step of preparing a catalyst precursor slurry containing molybdenum, bismuth and iron and having a solid concentration of 30% by mass or less, a step of spray-drying the catalyst precursor slurry at a drier inlet temperature of 120 C. to 240 C. to thereby obtain a dried particle and a step of calcining the dried particle at 500 to 750 C.

The invention relates to titanium oxide aerogels, in particular to titanium oxide binary or ternary (e.g. titanium oxide-carbon) aerogel monoliths possessing ordered meso- and macroporosity. The porous scaffold can be made with or without addition of binders and/or surfactants. The aerogel obtained by this method has a specific surface area greater than 60 m2/g and porosity larger than 60%. The surface area ranges from 60 to 300 m2/g. The porosity can reach as high as 99.6%. The size of the titanium oxide crystals are between 5 nm and 100 nm. The aerogel contains 100% titanium oxide. The composite (binary or ternary) aerogel can be prepared by adding at least 10% carbon in the form of (carbon nanotubes, carbon nanofibers, carbon microfibers, exfoliated graphene, cellulose fibers, polymer fibers, metallic and metal oxide nano and microfibers etc.). The aerogel can be prepared with a predeterminable shape. It can be shaped in a mold having a shape of a cylinder, cube, sheet or sphere. The aerogel can be also transformed into a supported or self-standing film with a thickness. The material can be used as a self-cleaning filter e.g. in a solar-thermal water and air purification system, in mesoscopic solar cells e.g. dye sensitized solar cells, multifunctional filler in polymer composites, in ceramics, in metals, thermoelectric material to convert (waste) heat into electricity, heat insulation material and electrode material in lithium ion batteries and supercapacitors.

A catalyst for oxidising ammonia comprises a selective catalytic reduction (SCR) catalyst and a composite heterogeneous extruded honeycomb having longitudinally extending parallel channels, which channels being defined in part by channel walls having a total longitudinal length, wherein the channel walls comprise a pore structure including a periodic arrangement of porous cells embedded in an inorganic matrix component, at least some of which porous cells are defined at least in part by an active interface layer of a catalytically active material comprising a precious metal supported on particles of a support material.

This invention relates to a composite composition for harmful gas removal containing a copper-manganese catalyst, which is capable of removing ambient and indoor pollutants, such as carbon monoxide and volatile organic compounds, the composite composition including a copper-manganese composite catalyst hybridized with an inorganic layer compound, an inorganic filler, activated carbon, and a binder.

A method for the catalytic conversion of ketoacids, including methods for increasing the molecular weight of ketoacids, the method comprising the steps of providing in a reactor a feedstock comprising at least one ketoacid. The feedstock is then subjected to one or more CC coupling reaction(s) in the presence of hydrogen, and in the presence of a catalyst system having both hydrogenation activity and CC coupling activity.